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1985 - Mycological Society of America

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<strong>Mycological</strong> <strong>Society</strong><br />

<strong>of</strong> <strong>America</strong><br />

NEWSLETTER<br />

Vol. 36 No. 1 June <strong>1985</strong>


SUSTAINING MEMBERS<br />

ANALYTAB PRODUCTS<br />

TED PELLA, INC. (PELCO)<br />

CAMSCO PRODUCE COMPANY,INC.<br />

PFIZER,<br />

INC.<br />

CAROLINA BIOLOGICAL SUPPLY<br />

PIONEER HI-BRED INTERNATIONAL, INC.<br />

DEKALB-PFIZER GENETICS<br />

THE QUAKER<br />

OATS COYPANY<br />

DIFCO LABORATORIES<br />

ROHM AND HAAS COYPANY<br />

HOFFMAN-LA<br />

ROCHE INC.<br />

SCHERING CORPORATION<br />

LANE SCIENCE EQUIPMENT COMPANY<br />

ELI LILLY & COMPANY<br />

MERCK SHARP AND DOHYE RESEARCH LABS<br />

SMITH KLINE & FRENCH LABORATORIES<br />

SOUTHWEST MOLD AND ANTIGEN LABS<br />

SPRINGER-VERLAG NEW YORK<br />

MILES LABORATORIES<br />

SYLVAN SPAWN LABORATORY,<br />

INC.<br />

NALGE COMPANY/SYBRON CORPORATION<br />

TRIARCH,<br />

INC.<br />

NEW BRUNSWICK SCIENTIFIC COMPANY<br />

WYETH LABORATORIES<br />

The <strong>Society</strong> is extremely grateful for the support <strong>of</strong> its Sustaining<br />

Members. These organizations are listed above in alphabetical order.<br />

Patronize them and let their representatives know <strong>of</strong> our appreciation<br />

whenever possible.<br />

OFFICERS OF THE MYCOLOGICAL SOCIETY OF AMERICA<br />

Officers<br />

Councilors<br />

Henry C. Aldrich, President Sandra Anagnostakis (1983-85)<br />

Roger D. Goos, President-elect Martha Christiansen (1983-86)<br />

James M. Trappe, Vice-president Alan Jaworski (1983-87)<br />

Harold H. Burdsall, Jr., Secretary Richard E. Yoske (1983-86)<br />

Amy Y. Rossman, Treasurer David Malloch (<strong>1985</strong>-88)<br />

Richard T.,.Hanlin, Past President (1984) Gareth Morgan-Jones (1983-86)<br />

Harry D. Thiers, Past President (1983) Francis A. Uecker (1982-85)


MYCOLOGICAL SOCIETY OF AMERICA NEWSLETTER<br />

Volume 36, No. 1, June <strong>1985</strong><br />

Walter J. Sundberg, Editor<br />

Department <strong>of</strong> Botany<br />

Southern Illinois University<br />

Carbondal e, I1 1 i noi s, 62901<br />

(618) 536-2331<br />

TABLE OF CONTENTS<br />

Sustaining Members .......... i<br />

Officers <strong>of</strong> the MSA ......... i<br />

Table <strong>of</strong> Contents .......... 1<br />

Editor's Note ............ 1<br />

General Announcements ........ 2<br />

Calender <strong>of</strong> Meetings and Forays ... 3<br />

Forthcoming Courses ......... 4<br />

New <strong>Mycological</strong> Research ....... 5<br />

Fungi for Distribution ........ 6<br />

Fungi Wanted ............. 7<br />

Identi fications ........... 10<br />

Publications Available ........ 11<br />

New Sooks by MSA Members ....... 12<br />

Pub1 ications Wanted ......... 13<br />

Annual Yeeti ng Program ........ 14<br />

Annual Meeting Abstracts ....... 15<br />

Uni v. 41 berta Mold Herbarium ........ 45<br />

Computer S<strong>of</strong>tware Available ........ 46<br />

MSA Placement Service ........... 46<br />

Travels and Visits ............. 50<br />

Assistantships and Fellowships Available . . 51<br />

Vacancies for Mycologists ......... 52<br />

Positions Wanted .............. 53<br />

Changes in Affiliation or Status ...... 54<br />

Papers, Seminars, Symposia, and Workshops . 55<br />

Honors, Awards, and Promotions ....... 56<br />

Personal News .. + ............ 57<br />

Associations and Clubs ........... 57<br />

Notes and Comments ............. 58<br />

Changes <strong>of</strong> Address for Respondence ..... 60<br />

Affi 1 iated Societies ............ 61<br />

EDITOR 'S NOTE<br />

This issue contains the program (pg. 14) and abstracts (pgs. 15-45). Your attention is<br />

also called to the announcement and application form for the new MSA Placement Service (pgs.<br />

46-49) and to the advertisement from Far West Fungi on page 53. A special note to a1 1 MSA<br />

Newsletter contributors is included on page 54.<br />

Unless otherwise noted, a1 1 creative fi 1 lers (art, poetry, etc.) included are heret<strong>of</strong>ore<br />

unpublished. Gareth Morgan-Jones prepared the cover "medley". The drawings were done by Jean<br />

J. Sang1 ier via J. W. Bennett (pg. 9), Christopher Best (pg. 12), and Yves Renaud (back cover).<br />

With permission from David Minter, the poetry (pgs. 9 & 15) is reprinted from the BMS Foray<br />

Programne, April <strong>1985</strong>. Finally, we thank Royal1 T. Moore for the submission <strong>of</strong> numerous<br />

"my~010gi~m~" (one-1 iners), some <strong>of</strong> which grace these pages.<br />

In order to conserve space (and reduce cost), readers are encouraged to use the MSA<br />

Di rectory for addresses where thei r response is requested. Mycol ogi sts, however, seem almost<br />

nomadic, sometimes making this approach difficult. Therefore, in this issue we are trying a new<br />

partial solution this problem (see pg. 60). Please make the included changes in your Directory<br />

as they will not appear in future Newsletter issues.<br />

Lastly, I wish to acknowledge the able and pleasant assistance <strong>of</strong> Linda Neuman who typed<br />

most <strong>of</strong> this issue and helped master our new letter qua1 ity printer. The ever-cooperative labor<br />

provided at mailing time by the SIU-C Mycology graduate students is also appreciated.


GENERAL ANNOUNCEMENTS<br />

ATTENTION BRITISH MEMBERS<br />

Dave Minter reminds MSA members in sterling areas that they can avoid bank charges in<br />

converting their MSA subscription to dollars by sending subscriptions in sterling to him at<br />

C.M.I., Ferry Lane, Kew, Surrey, TW9 3AF, U. K. Calculate the value <strong>of</strong> your subscripion using<br />

the dollar/sterling rate in the newspaper <strong>of</strong> the day you post the subscription, and please make<br />

sure your 1986 subscription arrives at the C.Y.I. by 1 January 1986.<br />

MSA PLACEMENT SERVICE<br />

Prospective graduates in mycology seeking employment are urged to register with the MSA<br />

Placement Service by completing the Employee Data Form published elsewhere in this issue <strong>of</strong> the<br />

MSA Newsletter. Data on prospective employees are provided to potential employers where thei r<br />

qualifications meet job requirements. Likewise, persons seeking employment are provided with a<br />

printout <strong>of</strong> vacant positions that match their training. Inqui ries regarding the service should<br />

be addressed to either Gareth Morgan-Jones, Auburn University, or Me1 vin S. Fuller, University<br />

<strong>of</strong> Georgia.<br />

TEACHING CULTURES<br />

Those who teach mycology should be aware that an array <strong>of</strong> identified fungal cultures are<br />

available for teaching purposes from the <strong>America</strong>n Type Culture Collection for $12 a piece. A<br />

catalog <strong>of</strong> these cultures and their uses can be obtained free <strong>of</strong> charge from the ATCC.<br />

THE MYCOLOGY GUIDEBOOK<br />

For several years we have been working, albeit rather slowly, toward a revision <strong>of</strong> the<br />

Mycology Guidebook. It seems appropriate now that we actual ly start thinking about the<br />

organization <strong>of</strong> the new edition and its contents. This requires that members <strong>of</strong> the MSA get<br />

involved in terms <strong>of</strong> their ideas and input, as well as writing parts <strong>of</strong> the text. Below are<br />

some questions which are merely guidelines for getting started. Other comments w i l l be<br />

welcomed with enthusiasm!<br />

1. Are you interested in writing part(s) <strong>of</strong> the new edition <strong>of</strong> the Vycology Guidebook?<br />

2. Did you write one or more sections <strong>of</strong> the present edition.?<br />

3. How useful have you found the present Guidebook?<br />

4. Which subject areas should be added to the text?<br />

5. Which, if any, subject areas might be deleted?<br />

6. Do you have any suggestions on the organization <strong>of</strong> the materials included in the text? For<br />

example, is the present organization (i.e.,<br />

the categories <strong>of</strong> General Information,<br />

Taxonomic Groups, Ecological Groups, Fungi as Bi 01 ogical Tools, and the accompanying<br />

Appendices) a good format?<br />

7. It has been suggested that the new edition <strong>of</strong> the Guidebook be published in Spanish as well<br />

as English. Do you agree or disagree with this idea?<br />

Please send comments to these questions as well as other suggestions, etc. to J. Ammirati,<br />

Chair, Mycology Guidebook Committee, Department <strong>of</strong> Botany, KB-15, University <strong>of</strong> Washington,<br />

Seattle, WA 98195.<br />

TO ALL MYCOLOGICAL WRITERS<br />

The MYCOLOGIA MEMOIRS Committee wants book-length manuscripts for review. Contact T. M.<br />

Hammill for details.


CALENDAR OF MEETINGS, FORAYS, AND WORKSHOPS<br />

August <strong>1985</strong><br />

1-4 The Annual Meeting and foray <strong>of</strong> the NORTH AMERICAN MYCOLOGICAL ASSOCIATION<br />

(NAMA) will be hosted by the <strong>Mycological</strong> Association <strong>of</strong> Washington (MAW), and<br />

will be held at Canaan Valley Resort State Park near El kins, West Virginia.<br />

Kent H. McKnight will serve as head foray mycologist with numerous other guest<br />

speakers and workshop leaders from the YSA membership. <strong>Mycological</strong> and other<br />

resort activities will abound (I plan to bring my roller sk6tes--ed.)<br />

Registration: $60.00. Meals $65.00. Room $44-$120.00. Contact Frances Usenik,<br />

2327 49th Street, NW, Washington, DC 20007.<br />

<strong>1985</strong> ANNUAL MEETING OF THE SOCIETY OF INDUSTRIAL MICROBIOLOGY will be held at<br />

the Westin Hotel, in Copley Place, Boston, MA. For more information contact:<br />

Forrest S. Yoy, Morton Thiokol , Inc., Ventron Division 150 9ndover Street,<br />

Danvers, MA 01932; Phone (617) 774-3100 or Stephen W. Queener, Research<br />

Associate, Eli Lilly and Company, Indianapolis, IN 46285; Phone (317) 261-7454.<br />

TENTH ANNUAL NORTHEASTERN MYCOLOGICAL FORAY will be held at the State University<br />

<strong>of</strong> New York, Oneonta, NY. Principal mycologists will be David Malloch,<br />

University <strong>of</strong> Toronto, David Pegler, Royal Botani cal Gardens, Kew England, and<br />

Currie Marr, State University <strong>of</strong> New York. For more information contact: Pat<br />

and Jim Kronick, 1951 Lowell Lane, Merrick, NY 11566.<br />

BMS SON OF TRUFFLE HUNT will be held at Cotswolds. Contact Jane Ingham, 21<br />

Loughmi 11 Road, Pershore, Worcestershi re.<br />

TELLURIDE MUSHROOM CONFERENCE. Foray in forests surrounding Tell uri de, an<br />

historic Colorado mining town. Courses include mushroom identification,<br />

cul ti vation, and ethnomycol ogy. For further information contact: Emanuel<br />

Salzman, P. 0. Box 5503, Denver, CO 80217-5503. Phone: (303) 296-1218.<br />

1-18 MUSHROOM STUDY TOUR OF THE HIMALAYAS. Organized by Gary Linc<strong>of</strong>f, Andrew Weil<br />

and Emanuel Salzman. Foray in the forests surrounding the hill stations, the<br />

beautiful old summer resorts <strong>of</strong> the British colonial days, in the foothills <strong>of</strong><br />

the great Himalayas. For more information contact: Emanuel Salzman, P. O.Box<br />

5503, Denver, CO 80217-5503. Phone: (303) 296-1218.<br />

BMS AUTUMN FORAY will be held at Chester.<br />

Contact Dave Minter for details.<br />

THE A. H. SMITH FORAY will be held near Baraboo, Wisconsin. Contact Jan Phelps:<br />

UWC-Baraboo, 1006 Connie Road, Baraboo, W I 53913.<br />

The Westwater Inn, Olympia, Washington, will be the site <strong>of</strong> the WESTERN<br />

INTERNATIONAL FOREST DISEASE WORK CONFERENCE. For particulars contact: Ken<br />

Russel 1 , Dept . o f Natural Resources, Di vision <strong>of</strong> Pri vate Forestry and<br />

Recreation, MQ-11, Olympia, WA 98504; (206) 545-0953; or Walt Thies, USDA<br />

Forest Service, Forestry Sciences Laboratory, 3200 Jefferson Way, Corvall is, OR<br />

97331; (503) 757-4396.<br />

32ND CHARLES HORTON PECK ANNUAL MYCOLOGICAL FORAY will be held in the Arnot<br />

Teaching and Research Forest <strong>of</strong> Cornell University, located in Van Etten, New<br />

York. For more information and/or reservation forms contact: R. P. Korf, PECK<br />

FORAY COORDINATOR, Plant Path01 ogy, Cornel 1 University, Ithaca, NY 14853.


4<br />

October - <strong>1985</strong><br />

BMS MINI-FORAY IN SPAIN (Barcelona, Catalonia, and Monseny). Yrite David Minter<br />

or Henry Descal s, Department de Botani ca, Facul tat de Bi 01 ogi cas, Uni versi tat de<br />

Barcelona, Diagonal 645, Rarcel ona 08028, Spain.<br />

THE OREGON MYCOLOGICAL SOCIETY FALL FORAY will be held along the northern Oregon<br />

Coast. Guest mycologist will be Joseph Ammirati. For information on the<br />

location contact J. Preston Alexander, Rt. 1, Box 158, Forest Grove, OR 97116.<br />

November <strong>1985</strong><br />

23<br />

April 1986<br />

BMS Meeting on TOXIC FUNGI at ~odrell' Laboratories, Kew.<br />

to learn more.<br />

Contact David Minter<br />

7-10<br />

THE HKITISH MYCOLOGICAL SOCIETY GEhERAL MEETING in Bristol. Topic:<br />

"Evolutionary Biology <strong>of</strong> the Fungi ." Learn more from David Minter.<br />

23-27<br />

BMS SPECIALIST WORKSHOP ON ASCOMYCETES will occur at CMI.<br />

Contact David Minter.<br />

May - 1986<br />

3-4<br />

MID-ATLANTIC STATES MYCOLOGY CONFERENCE is tentatively set at Towson State<br />

College, Towson, Maryland. Interested persons should contact Jerry Motta, Dept.<br />

<strong>of</strong> Botany, University <strong>of</strong> Maryland, College Park, MD 20742.<br />

BMS ANNUAL SPRING FORAY (jointly held with the Botanical <strong>Society</strong> <strong>of</strong> Edinburgh)<br />

wi 11 be in Gal loway, based at Newton Stewart. Write Alan Bennell , Royal Botanic<br />

Garden, Edinburgh.<br />

August 1986<br />

30-Sept. 4<br />

FOURTH INTERNATIONAL FUNGAL SPORE SYMPOSIUM wi 11 be he1 d in Scot1 and (Sti rl i ng<br />

University). The host wi 11 be John Smith, University <strong>of</strong> Strathclyde, Glasgow,<br />

Scot 1 and.<br />

FORTHCOMING COURSES<br />

David Minter and Paul Cannon wi 11 conduct an international course on ASCOPIYCETE TAXONOMY,<br />

7-18 October <strong>1985</strong>, at the Universidad Austral de Chi le, Valdivia, Chile. Further information<br />

is avai 1 able from Dr. H. Peredo, Instituto Silvicul tura, Uni versidad Austral, Casi 11 a 567,<br />

Valdivia, Chile.<br />

MUSHROOM TOXICOLOGY will be <strong>of</strong>fered by N. S. Weber & K. Cochran, Sept. 15-21 at Dillman's<br />

Sand Lake Lodge, Lac Du Flambeau, W I 54538.<br />

N. S. Weber will teach MUSHROOMS OF SLEEPING BEAK DUNES, July 22-26, at the Leelanau<br />

Center for Education, Glen Arbor, MI 49636.<br />

WOOD DETERIORATION, Fall Quarter <strong>of</strong> <strong>1985</strong>, (3 cr.). by Elmer L. Schmidt, Department Forest<br />

Products, University <strong>of</strong> Minnesota, St. Paul, MN 55108<br />

A MUSHRUMF'US - AN MSA FORAY


NEW MYCOLOGICAL RESEARCH<br />

G. C. ADAMS: Genetics <strong>of</strong> virulence and hypovirulence <strong>of</strong> Leucostoma persoonii and -- L. cincta<br />

(anamorphs: Cytospora spp. ).<br />

J. P. ALEXANDER: The effects <strong>of</strong> endogenous growth regulators on the growth and differentiation<br />

<strong>of</strong> a range <strong>of</strong> wild fleshy fungi.<br />

W. C. HAKEWELL: Studies on color guides, color standards, and color dictionaries.<br />

P. R. BECKJORD: Survey <strong>of</strong> the ectomycorrhizal epigeous fungi <strong>of</strong> oaks and conifers on surface<br />

mines and - in forests <strong>of</strong> western Mary1 and and factors for their ecology, sociology, and<br />

phaenol ogy .<br />

T. SEGAN: The genus Amanita in southern Illinois.<br />

S. E. CARPENTER: Revision <strong>of</strong> the ~hialeoideae and Ombrophiloideae (Helotiales, Leotiaceae).<br />

M. A. CASTELLANO: Monograph <strong>of</strong> Hysterangium.<br />

M.-M. CHEN: Epidemiology <strong>of</strong> white pine blister rust <strong>of</strong> sugar pine and the study <strong>of</strong> resistance<br />

<strong>of</strong> Pinus radiata to western gall rust: identification <strong>of</strong> fungal pathogens; ecology <strong>of</strong> and<br />

resistance to tree rusts; and edible fungi <strong>of</strong> China.<br />

P. K. DUBLISH: Aeromycological studies <strong>of</strong> a stud-farm.<br />

D. H. PFISTER: An inventory <strong>of</strong> the <strong>Mycological</strong> Literature from 1753 to 1821 with Jean Boise as<br />

Research Bibliographer.<br />

G. C. YAYE (with D. H. Pfister & Jean 8oise): <strong>Mycological</strong> Literature.<br />

R. KENDRICK: Pathogenicity <strong>of</strong> Hyphomycetes to Spruce Budworm; model ing the impact <strong>of</strong><br />

herbicides on pond ecosystems; morphology and taxonomy <strong>of</strong> VAY fungi ; and use <strong>of</strong><br />

biotechnology and a dual fungal culture to produce lipids from cellulosic wastes.<br />

R. W. YERRIGAN: Relationships in Agaricus (sub) section Hortenses.<br />

R. KOFFMAN: Studies on Aspergi 11 us clavatus and Psi locybe tampanensi s.<br />

R. K. S. KUSHWAHA: Biology <strong>of</strong> Chrysosporium and allied fungi from soil with special reference<br />

to their morphology and taxonomy.<br />

G. LIM: Fungal enzymes; production <strong>of</strong> aroma chemicals by fungi.<br />

P. D. MILLNER: Interactions among saprophytic root-colonizing bacteria and fungi, and VA<br />

mycorrhi zae that affect plant nutrition; protein and enzyme analysis <strong>of</strong> VA mycorrhizae and<br />

Endogone as related to growth, colonization, and nutrient translocation.<br />

G. M. MUELLER (with Stephen Rehner): DNA-DNA hybridization as a means for studying<br />

phylogeneti c re1 ati onshi ps among species <strong>of</strong> Laccari a.<br />

M. E. NOOKDELOOS: Taxonomy and ecology <strong>of</strong> Agarics from Boreal and Arctic regions (esp.<br />

Entolomataceae, Tricholomataceae). Entoloma sensu lato in eastern Canada and northeastern<br />

USA.<br />

S. L. PEELE: New compounds for anti-tumor and anti-cancer activity from mushrooms.<br />

S. A. REHNER: Taxonomy <strong>of</strong> A roc be sect. Pediadeae and a phylogenetic analysis (based on<br />

mol ecul ar approaches) +b$-<br />

o rocybe sect. Pedi adeae including comparisons to selected taxa<br />

within the Bolbiticeae.


E. L. SCHMIDT: Shiitake yields on red and bur oak, effects <strong>of</strong> white rot fungi on bonding<br />

systems <strong>of</strong> aspen waferboard, and the influence <strong>of</strong> aliphatic acids on spore germination <strong>of</strong><br />

wood decay fungi.<br />

M. SPEAR: Media and techniques for large-scale production <strong>of</strong> ectomycorrhizal inoculum.<br />

W. J. SUNDBERG (with Raafat Mohamnadkhani ): lJl trastructural development and hi stochemi stry <strong>of</strong><br />

clamp connection formation in Cyathus 01 la. -<br />

3. M. TRAPPE: Hypogeous fungi and their mycorrhizae--comparison <strong>of</strong> Spain with Oregon and<br />

Cal i fornia (grant from I1.S.-Spain Cooperative Research Awards) ; mycorrhiza-Rhizobium<br />

interactions in tropical woody legumes (Indo-U.S. Science & Technology Initiative Awards).<br />

R. C. ULLRICH: The following are studying the aspects <strong>of</strong> biology in Schizophyllum in Ull rich's<br />

Lab; Eunice Fruel i ger--0rotidine-5 ' -monophosphate decarboxylase and its gene; Brent<br />

Suckner--ri bosomal RNA genes ; Lisa Phel ps--cytochrome oxidase suhuni t I I mi tochondri a1<br />

gene from; Charles Specht--mappi ng mi tochondri a1 genes; and A1 fredo Munoz--tryptophan<br />

brosynthesi s.<br />

D. WEBER (with Vic Bundersoa): Development <strong>of</strong> an interactive video disc for a visual<br />

identification key to mushrooms (Exxon Educational Foundation Grant).<br />

W. YUN: Taxonomy <strong>of</strong> hypogeous fungi in China.<br />

BASIDIOMYCETES<br />

J. P. Alexander can provide Pleurotus ostreatus (wild types from the Pacific Northwest), and<br />

other Pleurotus sp., and a1 so cul-calvatia booniana (Pacific Northwest).<br />

M. A. Caste1 lano will send Hysterangium specimens.<br />

M.-M.<br />

Chen has stored spores <strong>of</strong> Endocronartium (western gal 1 rust).<br />

P. K. Dub1 ish <strong>of</strong>fers Phyllacteria dal bergiae on leaves <strong>of</strong> Dal bergra sisso (preserved material ).<br />

S. L. Peele has dried specimens, cultures, and spores f rom4mani ta phal loides, A. muscari a,<br />

Pleurotus sapidus as well as many species <strong>of</strong> Psilocybe and Panacolus. sea for free<br />

i nformation or call Florida Mycology ~esearch--904) 478-3912.<br />

R. E.<br />

I<br />

Tulloss <strong>of</strong>fers specimens <strong>of</strong> Amanita spp. from the pine Barrens <strong>of</strong> New Jersey (largely<br />

section Lepi dell a).<br />

MISCELLANEOUS<br />

K. Diebolt has cultures <strong>of</strong> ectomycorrhizal fungi--send for a list.<br />

A MUSHRUMOR - A HIiVT OF ANOTHER NAME CHANGE FOR THE CO!.!MERCIAL MUSHROOM


FUNGI WANTED<br />

ACRASIOVYCETES<br />

R. L. Blanton: Cultures <strong>of</strong> Copromyxa protea.<br />

MYXOMYCETES<br />

K. L. Rraun: Myxomycete specimens from Mexico.<br />

T. W. Gaither: Collections <strong>of</strong> any Didymium species.<br />

H. W. Kel ler: Myxomycetes--speci es <strong>of</strong> the genera Peri chaena and Li cea; corticol ous myxomycetes<br />

from 1 i vi ng trees and vines; myxomycetes from Mexico; specimens <strong>of</strong> Licea fimicol a (common<br />

on dung from herbivorous animal s--cow, bison, horse).<br />

S. L. Stephenson : Myxomycetes, especially col lections from western North <strong>America</strong>.<br />

OOMYCETES<br />

H. H. Ho: Phytophthora japonica (P. - oryzeae), and Phytophthora areceae (A1 type).<br />

ZYGOYYCETES<br />

B. Yendrick (with M. Srundrett): Wishes to exchange pot cultures or spores <strong>of</strong> VAM fungi.<br />

J. M. Trappe: Specimens <strong>of</strong> Endogonaceae.<br />

ASCOMYCETES<br />

G. C. 4dams: Recent collections <strong>of</strong> Leucostoma and Valsa with host identifications.<br />

S. E. Carpenter: Cultures and specimens <strong>of</strong> any Phial eoi deae and Ombrophi 1 oideae (He1 oti ales,<br />

Leot i aceae ).<br />

K. Di ebol t : Cultures <strong>of</strong> Wynnea ameri cana .<br />

K. Esser: The perfect stage <strong>of</strong> the Ascomycete Cochliobolus lunatus.<br />

J. H. Hai nes: Specimens <strong>of</strong> Hyal oscyphaceae.<br />

M. Harrington: Recently collected, ai r-dried specimens <strong>of</strong> Sarcoscypha to culture. Please ship<br />

. . by overnight delivery system, and they shall gladly reimburse costs. Send c/o L. R.<br />

Batra, Rm. 313, Bldg. OllA, USDA, Re1 tsvi 1 le, MD 20705. Telephone 301-344-2317 (call<br />

collect) for any needed information on how to collect or ship these fungi.<br />

T. Iturri aga: Cultures or specimens or both <strong>of</strong> Strossmayeria (Helotiales) and its anamorph<br />

Pseudospi ropes.<br />

L. M. Kohn: Cultures and specimens <strong>of</strong> sclerotium-forming Ascomycetes.<br />

H. J. Kronenberg: Cordyceps si nensi s and Cordyceps ci cadae<br />

J. M. Trappe: Specimens <strong>of</strong> hypogeous Ascomycetes.


W. Zhuang: Discomycetes (with pigmented apothecia) on fungi.<br />

BASIDIOMYCETES<br />

J. P. Alexander: Cultures <strong>of</strong> Ramaria botrytis, Sparassis crispa, 2. radicata, HerIcium<br />

abieti s, Fistul ina hepatica, Vol variel la bombyci na, and Agari cus augustus.<br />

J. Ammi rati : Corti nari us, subgenera Dermocybe, Leprocybe, and Yyxaci um with notes and/or<br />

kodachromes. Yelanotus with note's and/or kodachromes and spore deposits for culture work.<br />

0. Bermudes: Cultures <strong>of</strong> Amanita spp. He would also like cultures <strong>of</strong> known ectomycorrhiza<br />

formers and dried specimens <strong>of</strong> amanitin- and phalloidin-containing mushrooms. He will pay<br />

postage.<br />

H. H. Surdsall : Armillaria mellea collections with complete notes as to field characters,<br />

suspected pathogenicity, and host; cultures, single spore isolates and any other<br />

information concerning the col lections.<br />

M. Caste1 lano: Cultures or specimens <strong>of</strong> Hysterangium (Phal laceae).<br />

K. Diebol t: Cultures <strong>of</strong> Gyrodon merul ioides and Sui 1 lus borinus.<br />

M. F. Doyle: Pacific Island agarics (notes preferred and/or photos, but he's a realist).<br />

R. E. Halling: Collybia and Marasmiellus. Notes on color and odor always helpful.<br />

R. W. Kerrigan: Cultures/spore prints <strong>of</strong> wild Agaricus bisporus and its close relatives.<br />

Vouchers, notes, and kodachromes appreciated.<br />

R. K<strong>of</strong>fman: Gymnopilus spectabilis.<br />

H. J. Kronenberg: Ganoderma lucidum, and Poria -- cocos.<br />

A. S. Yethven: Collections <strong>of</strong> Clavariadelphus from North <strong>America</strong> with color notes and spore<br />

deposits, and cultures <strong>of</strong> Clavariadelphus from Rorth Ameri ca.<br />

H. P. Mol itoris: Cultures <strong>of</strong> Yelanotaenium ruppiae (a marine basidiomycete, Usti laginales).<br />

M. E. Noordeloos: Specimens <strong>of</strong> Entoloma (sensu lato incl . Leptonia; Nolanea: Pouzarel la,<br />

Ecci 1 ia; A1 boleptonia). Notes and slides on fresh material are necessary!<br />

S. L. Peele: Cultures or spores <strong>of</strong> Psilocybe zapotecorum.<br />

J. Pfi ster: Recent exsiccatae and spore prints <strong>of</strong> Me1 anoleuca gramnopodia, - M. graminicola, - M.<br />

verrucipes, - M. subal pina, and - M. subbrevipes for enzymatic studies.<br />

D. Prusso: Specimens <strong>of</strong> Tulostoma from North <strong>America</strong> including collection data.<br />

S. Rehner: Cultures and/or spore prints plus voucher specimens (notes & photos; if possible)<br />

<strong>of</strong> Agrocybe, Bol bi tius, Conocybe, Gastrocybe (especially Agcocybe pediades, A.<br />

subpediades, 4. semiorbiaclaris, A. retigera, A. thinlenta, - A. arval is, - A.<br />

cyl indracalaegeri ta, Gastrocybe lareri tia, C o n o c y b m .<br />

M. Spear: Cultures <strong>of</strong> Agaricus subrufesceus and other unusual Agaricus spp.<br />

W. J. Sundberg: Lepiota spp. (sensu lato; notes and/or photographs helpful ).<br />

J. M. Trappe: Specimens <strong>of</strong> hypogeous Basidiomycetes.


R. E. Tulloss: We1 1 -documented collections <strong>of</strong> Amani t a spp. with slides if possible--please<br />

inquire, first.<br />

DEUTEROMYCETES<br />

W. D. Jennsen : Tri choderma vi ri de .<br />

R. K<strong>of</strong>fman : Aspergi 11 us cl avatus.<br />

R. K. S. Yushwaha: Cultures <strong>of</strong> Chrysosporium, Arthroderma, and Halbranchea.<br />

J. Y. McPartland: Cultures <strong>of</strong> any race (1 thru 6) <strong>of</strong> Fusarium oxysporum F. sp. vasinfectum.<br />

M. Wingfiel d: Leptographi um spp., Verti ci cl adiel 1 a spp., and Phial ocephal a spp.<br />

MISCELLANEOUS<br />

G. Guzman: Duplicates for the Herbarium <strong>of</strong> INIREB (XAL).<br />

W. Lanier: Cultures <strong>of</strong> any fungus which parasitizes pest insects or nematodes. Contact him at<br />

BIOSIS, 3788 Fabian Way, Palo Alto, CA 94303.<br />

R. E. Scott: Cultures <strong>of</strong> psychrophil ic fungi. Please contact him by letter with culturing<br />

conditions, etc. before sending (See Changes <strong>of</strong> Address).<br />

J. F. White & Garry T. Cole: Endophytic fungi from grasses <strong>of</strong> North <strong>America</strong>.<br />

To An Unwanted Ascomycete<br />

A fungus by a spore trap grew,<br />

A di scomycete fresh and new.<br />

And, heedless <strong>of</strong> its likely fate<br />

It soon began to sporulate.<br />

Its spores, released, flew in a trice<br />

Into my spore trap's orifice.<br />

Ah, waste! Its chosen situation<br />

Has spoiled all chance <strong>of</strong> propagation,<br />

And oh! My whole week's record messed<br />

With spores from this unwanted guest.<br />

Fool i sh Pezi za ! Better hide ,<br />

Or 1'11 deploy the fungicide!<br />

---Fel ici ty Jackson


10<br />

IDENTIFICATIONS<br />

The following are willing to identify the taxa specified.<br />

MYXOMYCETES<br />

H. W. Kel ler: Myxomycetes--species <strong>of</strong> Peri chaena and Licea, and corticolous myxomycetes.<br />

ZYGOMYCETES<br />

S. M. Berch: Vesi cular-arbuscul ar mycorrhi zal fungi ,. Endogonaceae<br />

J. M. Trappe: Endogonaceae.<br />

ASCOMYCETES<br />

S. E. Carpenter: Leoti aceae (He1 o ti ales).<br />

J. H. Haines: Hyaloscyphaceae.<br />

A. Y. Rossman: All members <strong>of</strong> the Hypocriales including Nectria and Gibberella as specimens or<br />

cultures forming ascocarps. Fresh specimens are preferred.<br />

L. J. Spielman: Val sa, Leucostoma, and the anamorphs in Cytospora.<br />

J. M. Trappe: Hypogeous Ascomycetes.<br />

BASIDIOMYCETES<br />

J. P. Alexander: Calvatia sp., and Pleurotus sp.<br />

M. A. Caste1 lano: Hysterangium<br />

G. P. Chamuris: Stereum S.S. or s.1.; temperate or tropical.<br />

M.-M.<br />

Chen : Cronartium, Coleosporium, Melampsora, Chrysomyxa; Lenzites, and Daedalea.<br />

R. E. Halling: Collybia and Marasmiellus.<br />

M. E. Noordeloos: Entoloma sensu lato (only possible with notes and slides).<br />

J. M. Trappe: Hypogeous Basidiomycetes.<br />

R. E. Tulloss: Amanita (Please inquire, first).<br />

W. Yun: Me1 anogaster<br />

DEUTEROMYCETES<br />

M.-M.<br />

Chen: Cytospora<br />

M. Wingfield: Leptographium spp.<br />

'<br />

"What's happened to the truffle hunterslr' rrTheyrve gone underground. "


PUBLICATIONS AVAI LABLE--FOR GIVE-AWAY, SALE, OR EXCHANGE<br />

11<br />

Gaston Guzman has the following for exchange or sale: SULLETIN OF THE MEXICAN SOCIETY OF<br />

MYCOLOGY, Vol . 19 (1984), 356 pages and 16 color plates. $15 US (back numbers are a1 so<br />

avai 1 able) .<br />

Machiel E. Noordeloos has reprints on Entoloma for sale or exchange. Send for a list.<br />

Joachim Schl iemann has available: Fries' ICONES SELECTAE HYMENOMYCETUM, 1/11; Persoon Is<br />

SYNOPSIS METHODICA FUNGOORUM 111 I ; Vai 1 lant Is BOTANICON PARISIENSE ; and a 1 arger number <strong>of</strong><br />

other duplicate titles. Send for list or specify desiderata.<br />

Christian Vol bracht has a list <strong>of</strong> duplicates from his mycological collection.<br />

Harold W. Keller has 4. E. Nannenga-Bremekamp's DE NEDERLANDSE NYXOYYCETEN, 1974, 2nd<br />

edition (with supplement).<br />

Richard Rlanton has for sale: AMERICAN JOURNAL OF ROTANY, Vols. 60 (1973) through 70<br />

(1983) for $4/volume plus postage. Also, JOURNAL OF PROTOZOOLOGY, Vols. 23 (1976) through 31<br />

(1984) for $51~01 ume plus postage.<br />

Mo-Mei Chen has for sale PRELIMINARY ANALYSIS OF THE RUST FLORA IN THE FOREST OF TIBET<br />

(abstract in Enqlish); THE GUIDE BOOK ON LABORATORY IDENTIFICATION OF PORE FUNGI (in Chinese);<br />

A NEW GENUS, ST~LBECHRYSOMYXA CHEN GEN NOV. <strong>of</strong> Chrysomyxaceae on Rhododendron, and THE INDEX.OF<br />

TREE DISEASES OF CHINA.<br />

Hi romi tsu Hagiwara wants to exchange the MYXOMYCETOUS WORLD by Hagiwara & Izawa, including<br />

ca. 80 excel lent color photographs with Japanese explanations, for any book(s) or reprint(s) on<br />

Myxomycetes .<br />

Donald T. Kowal ski has for sale originals <strong>of</strong> Lister's A MONOGRAPH OF THE MYCETOZOA, Vols.<br />

1, 2, & 3 for $350; and April 1926 NATIONAL GEOGRAPHIC (Watercolors <strong>of</strong> Slime Molds) for $10.<br />

Robert E. Macho1 has for sale MYCOTAXON, Vols. 1-20 and some old mushroom books--send for<br />

list.<br />

Stephen L. Peele has available one free issue <strong>of</strong> THE MUSHROOM CULTURE, The Journal <strong>of</strong><br />

Mushroom Cultivation (see Changes <strong>of</strong> Address).<br />

Richard W.<br />

Kerri gan has free information on easy classroom cultivation <strong>of</strong> Pleurotus.<br />

Philip A. Orpurt has for sale MYCOLOGIA, Vols. 41-64 (1949-1972) bound (Ch. brown) $8 each<br />

($192); and Vol s. 65-75 (1973-1983) unbound, $5 each ($55).<br />

Walter J. Sundberg will sell Sundberg & Richardson, MUSHROOMS AND OTHER FLESHY FUNGI OF<br />

LAND BETWEEN THE LAKES, 64 p., 98 color photos, 1980. Prepay $3.65 (includes postage and<br />

padded mai 1 i ng envelope).<br />

Jenifer Huang McBeath has a reprint for give away entitled SYYPTOMOLOGY ON SPRUCE TREES<br />

AND SPORE CHARACTERISTICS OF A BUD RUST PATHOGEN, Phytopathology 74:456-461, 1984.<br />

Dieter Schierenberg has special lists <strong>of</strong> books in Botany and Mycology.<br />

Prinsengracht 485-487, 1016 HP, Amsterdam, Holland.<br />

Write him at<br />

Rodham E. Tulloss has, for the cost <strong>of</strong> copying & postage, a BIBLIOGRAPHY & INDEX TO NORTH<br />

AMERICAN LITERATURE ON AMANITA with over 300 references, approx. 250 indexed, over 200 taxa.<br />

Herbert N. Humphrey has for sale a Periodical Library, chiefly mycological, also plant<br />

path01 ogical and botanical journal s dating from 1872. Examples include: ANNALES MYCOLOGICI ,<br />

Vols. 1-36; BULLETIN DE LA SOCIETE MYCOLOGIQUE DE FRANCE, Vols. 7, 11, 29, 35-55;<br />

PHYTOPATHOLOGY, Vol s. 1-59; AMERICAN JOURNAL OF BOTANY, Vol s. 16-23; and many more. For a<br />

complete list, write to Herbert N. Humphrey, 4040 Maybelle Avenue, Oakland, CA 94619.


Bryce Kendrick is <strong>of</strong>fering A YOUNG PERSONS' COLOURING HOOK OF FUNGI, THE FIFTH KINGDOM<br />

(avai 1 able this summer), THE ENCYCLOPEDIA OF MUSHROOMS, and several references on<br />

Deuteromycetes. Write him for a list.<br />

NEW BOOKS BY MSA MEMBERS<br />

The fol 1 owing announcements were recei ved in response to the MSA Newsletter questionnai re:<br />

Alan Bessette. <strong>1985</strong>. GUIDE TO SOME EDIBLE AND POISONOUS FUNGI OF NEW YORK. 41 color<br />

photographs and descriptions <strong>of</strong> fungi, many <strong>of</strong> which are found throughout the United<br />

States. A1 though designed for the novice, experienced collectors will also appreciate the<br />

color qua1 ity and diversity <strong>of</strong> specimens. Cost is $3.95 including postage and handl ing.<br />

Available from A1 an Bessette, Utica College <strong>of</strong> Syracuse Uni versity, 1600 Burrstone Road,<br />

Utica, NY 13502. Make checks payable to Otica College <strong>of</strong> Syracuse University.<br />

J. Cramer, has just received the manuscript for the fourth fully revised edition <strong>of</strong> Rolf<br />

Singer's THE AGAKICULES. Typesetting has been started, and publication is scheduled for<br />

winter <strong>1985</strong>-86.<br />

Nancy S. Weber & Alexander H. Smith. Photographs by Dan Guravich. <strong>1985</strong>. A FIELD GUIDE TO<br />

SOUTHERN MUSHROOMS. Avai lable from Uni veri si ty <strong>of</strong> Michigan Press, Ann Arbor, 48109.<br />

$16.50 less 10% pr<strong>of</strong>essional discount (+ 4% sales tax in MI), + $1.00 handl ing for first<br />

copy, $.25 for each additional copy.<br />

Kenneth B. Raper. 1984. THE DICTYOSTELIDS. Princeton University Press. 453 pp.,<br />

illustrated. $75.00.<br />

Joost A. Stalpers. 1983. A REVISION OF THE GENUS SPOROTRICHUM, Studies in Mycology No. 24.<br />

Centraal bureau voor Schimnelcultures, P. 0. Box 273, 3740 AG Baarn, The Netherlands. 105<br />

pp. hfl. 25.<br />

M. A. Schipper and Joost A. Stalpers. 1984. A REVISION OF THE GENUS KHIZOPUS, Studies in<br />

Mycology No. 25. Centraalbureau voor Schimmelcultures, P. 0. 273, 3740 AG Baarn, The<br />

Nether1 ands. 34pp. hf 1. 10.<br />

Randy Yolina. <strong>1985</strong>. PROCEEDINGS OF THE 6TH NORTH AMERICAN CONFERENCE ON MYCORRHIZAE.<br />

Published by the Forest Research Laboratory, Oregon State University. 471pp. $20.00 plus<br />

$2.25 for postage and handl ing. To order, send check payable to OSU College <strong>of</strong> Forestry,<br />

to Col lege <strong>of</strong> Forestry, Oregon State Uni versi ty, Corvall is, OR 97331-5704.


P. K. Dub1 ish needs pub1 ications on aeromycol ogical studies.<br />

PUBLICATIONS WANTED 13<br />

J. Schl iemann would 1 i ke important old books on mushrooms, iconographies, rare titles; he<br />

is also interested in all give-away, sale, or exchange lists.<br />

E. W. Smith is in need <strong>of</strong> the Index <strong>of</strong> Plant Diseases (USDA Handbook 165).<br />

C. Volbracht is looking for any books on Mycology printed before 1900.<br />

D. Bermudes needs Charles David Badham's ESCULENT FUNGUSES OF ENGLAND 1847.<br />

R. Critchfield, Sr. wants any reprints on identification, taxonomy, morphology, and<br />

ecology <strong>of</strong> myxomycetes, and is willing to reimburse for reprints and/or postage.<br />

R. K<strong>of</strong>fman would like to obtain a copy <strong>of</strong> THE GENUS ASPERGILLUS by Raper & Fennell.<br />

R. Y. S. Kushwaha needs publications on taxonomy, ecology <strong>of</strong> Chrysosporium and members <strong>of</strong><br />

Gymnoascaceae.<br />

R. E. Macho1 wants old mushroom books, including incomplete, very early works, if the<br />

parts on mushrooms are intact.<br />

R. E. Scott would like reprints and any information on microscopic psychrophilic fungi,<br />

(e.g.) culture conditions, enzyme purifications, and secondary products (See Changes <strong>of</strong><br />

Address ).<br />

R. W. Yerri gan needs literature on Agaricus and old spawn catalogs.<br />

S. L. Stephenson would like reprints on Myxomycetes.<br />

J. P. Alexander would like THE FUNGI by Gaumann; Wolf & Wolf's THE FUNGI, Academic Press;<br />

PUFFBALLS & THEIR ALLIES..by A. Smith; and A NEW MONOGRAPH ON PLEUROTUS by Yiller (?).<br />

R. L. Tulloss needs both volumes <strong>of</strong> C. H. Kauffman's AGARICACEAE OF MICHIGAN.<br />

T M. Hammi 11 would 1 i ke the CANADIAN JOURNAL OF BOTANY, 1981, Vol . 59; and Gaumann 's THE<br />

FUNGI: A DESCRIPTION OF THEIR MORPHOLOGICAL FEATURES AND EVOLUTIONARY DEVELOPMENT.<br />

M. F. Doyle would like reprints, etc. on insular mycology and long-distance fungal<br />

dispersal.<br />

Gui 1 lermo Rodri guez-Scherzer wishes reprints or books (pri nci pal ly on Polyporaceae sensu<br />

lato) free or in exchange for mexican fungi (Ascomycetes and Basidiomycetes). Contact him at<br />

Herbario Metropol itano (UAMIZ), Departamento de Biologia, Uni versidad Autonoma<br />

Metropol - i tana-Iztapal apa, Apartado Postal 47-017, Mexico, 0. F. 07800.<br />

T-shirts, with this design<br />

in white on deep Fusarium purple,<br />

are available from:<br />

Mycoproducts, P. 0. Box 3050<br />

P. o. Box 3050<br />

Durham, NC 27705-1050


MYCOLOGICAL SOCIETY OF AMERICA<br />

<strong>1985</strong> ANNUAL MEETING PROGRAM<br />

University <strong>of</strong> Florida, Gainesvil le, Florida<br />

Saturday, August 10<br />

All Day:<br />

Foray to San Felasco Hammock State Preserve and University <strong>of</strong> Florida's<br />

Horticultural Farm, Alachua County.<br />

Morni ng: Yi ni Symposium. Recent Advances in Cryotechnol ogy<br />

Afternoon: Workshop. Recent Advances in Cryotechnol ogy<br />

Sunday, August 11<br />

Morni nglEarly<br />

Afternoon:<br />

Late Afternoon<br />

and Evening:<br />

All Day:<br />

Foray to Lake Yize, Austin Cary Memorial Forest, Alachua Co.<br />

Foray to Cedar Key on Florida's Gulf Coast isightseeing and dinner included)<br />

Meeting <strong>of</strong> the MSA Council<br />

Monday, August 12<br />

Morning: Session 1. Contributed Papers. Taxonomy<br />

Session 2. Symposium. Factors Effecting Morphogenesis in Achlya<br />

Session 3. Posters. Ecol ogy, Morphol ogy , and Taxonomy<br />

Afternoon: Session 3. (continued)<br />

Session 4. Contributed Papers. Siochemistry and Physiology<br />

Session 5. Contributed Papers. Ecology<br />

Session 6. Symposium. Recent Trends in the Study <strong>of</strong><br />

Heterobasidi omycetes<br />

Evening:<br />

AIBS Plenary Session<br />

Tuesday, August 13<br />

Morning: Session 7. Contributed Papers. Morphology and Taxonomy<br />

Session 8. Symposium. Recent Advances in the Biology <strong>of</strong> the Cultivated<br />

Mushroom<br />

Session 9. Posters. Biochemistry, Cytology, Genetics, Medical Mycology,<br />

Physiology and Ul trastructure<br />

Afternoon: Session 9. (continued)<br />

Session 10. Contributed Papers. Cytology and Ul trastructure<br />

Session 11. Contributed Papers. Genetics and Taxonomy<br />

Session 12. .Symposi urn. Beta-Gl ucans: Thei r Biosynthesi s and Degradation<br />

Evening: Session 13. Nomenclature Open House and Discussion<br />

Wednesday, - August 14<br />

Morni ng :<br />

MSA Breakfast and Business Meeting<br />

Presidential Address. Henry C. Aldrich. From Taxonomy to<br />

Biochemistry - The Odyssey <strong>of</strong> a Myxomycetologist


Afternoon : Annual Lecture. Franz Oberwi nkler. Evolutionary Trends in Basidi omycetes.<br />

Session 14: Contributed Papers. Biochemistry and Physiology<br />

Session 15: Contributed Papers. Genetics, Taxonomy, and Ul trastructure<br />

15<br />

Evening:<br />

Awards Presentat ion and Soci a1<br />

Thursday, August 15<br />

Morning: Session 16: Contributed Papers. Cytology and Ul trastructure<br />

Session 17. Symposium. Observations on the Macromycetes <strong>of</strong> the Deep South<br />

and Gulf Coast Regions<br />

MSA MEETING NOTES<br />

Gerald Benny wants to make all attending this year's MSA Annual Meeting in Gainesville<br />

aware <strong>of</strong> the following points.<br />

It may be possible to arrange for (a) .pick up at the airport or bus station if using these<br />

modes <strong>of</strong> transportation and (b) some pre- or post-meeting field excursions to nearby collecting<br />

areas. Write or call Gerald Benny in advance for arrangements.<br />

For those arriving for field trips, appetites can be serviced at the Snack Bar on the<br />

second floor <strong>of</strong> the Reitz Union or <strong>of</strong>f campus on University Avenue (just north <strong>of</strong> the campus).<br />

Several places, which can be reached by car, are a1 so located on Archer Road (south <strong>of</strong> the<br />

campus ) .<br />

Bartram Room B-22, which wi 11 be used for specimen study, identification, display, etc.,<br />

will be open Saturday and Sunday evenings and Sunday during the day by arrangement. Jim<br />

Kimbrough's room (Bartram 218, West Wing) houses the Mycology Library and will serve as a<br />

resource room.<br />

ABSTRACTS<br />

Abstracts <strong>of</strong> the papers scheduled for presentation at the <strong>1985</strong> MSA Annual Meeting are<br />

included a1 phabetical ly by author on the following pages.<br />

Truffle Hunting<br />

The truffle's an elusive chap,<br />

he doesn't have a sti pe or cap!<br />

He doesn't have a gill or pore,<br />

or veil or ring or volva or.. .<br />

skeletal trama, what a miser!<br />

Yet still he makes good mycorrhiza!<br />

And if you open him then ee-bah<br />

gum! He's got a 1 ovely gleba!<br />

With every tree he will not grow,<br />

when Autumn comes, no flashy show.<br />

A modest fungus, that's for sure,<br />

all curled up in the forest floor.<br />

4 we1 1 -trained dog or truffle pig<br />

(they say) will scent him out and dig<br />

him up, though with his habits mild<br />

I s till prefer the truffle child!<br />

Black, white, or brown our truffles be,<br />

too small and soily for your tea.<br />

So gastronomes must go abroad,<br />

to eat the truffle perigord.<br />

But to the beech woods take your rake<br />

and clear the leaves and start to<br />

scrape:<br />

they're fun to fine in their own way,<br />

so come on, join our next foray!<br />

---Jane Ingham


Adarns, G. M. W., see Rlackwell, M.<br />

G.R. ALlAGA and J. POMMERVILLE. The Department <strong>of</strong><br />

B~ology, Texas A&M IJnt versity, College Station, TX<br />

77843. Characterizat~on <strong>of</strong> the ktnetosomal region in the<br />

zoospores <strong>of</strong> Allomyces macrogynus.<br />

The aquatic fungus, Allomyces macrogynus, possesses<br />

unlflagllate zoospores with a slngle functional kinetosome<br />

(basal body) closely associated with the nucleus, the<br />

flagellar rootlet, and the basal mitochondr~on. This study<br />

was undertaken in an effort to determine more precisely<br />

the structure, orientation, and cornposition <strong>of</strong> the rootlet.<br />

Electron micrographs show that the rootlet is located next<br />

to that portion <strong>of</strong> the klnetosome which contains the<br />

characteristlc cartwheel structure. In longitudinally and<br />

transversely sectioned zoospores, the rootlet is composed<br />

<strong>of</strong> three electron dense bands, each separated by loosely<br />

packed fibrillar material. The outer band <strong>of</strong> the rootlet is<br />

adjacent to the basal mttochondrion whlch partially<br />

surrounds the rootlet while the inner band is linked to the<br />

kinetosome by short repeating extensions. The posterior<br />

portion <strong>of</strong> the nucleus is closely associated with the<br />

klnetosome forming an extension Into the most proximal<br />

region. Zoospores were osmotically lysed or mechanically<br />

disrupted in order to isolate the kinetosome fraction by<br />

density gradient centrif ugatlon. L~ght and electron<br />

microscopy <strong>of</strong> thls fraction showed that the kinetosome<br />

was separated w~th the nucleus, nuclear cap,<br />

cap-associated mitochondria, basal m~tochondrion, and<br />

flagellar rootlet, indicating that these organelles are<br />

associated with the kinetosome. Two-dtmensional<br />

polyacrylamide gel electrophores~s was performed on the<br />

kinetosomal fractions in order to characterize the proteins<br />

present. Further puriftcatlon <strong>of</strong> the kinetosome and the<br />

associated rootlet IS needed in order to determine the<br />

molecular composition <strong>of</strong> the structures.<br />

Arnerson, H. V., see Gray, 0. J.<br />

Arnrnirati , J. F., see Muel ler, G. M., et. a1 .<br />

Anderson, J. R., see Hintz, W. E., et. al.<br />

Anderson, J. R., see Meyer, R. J., et. al.<br />

J.B. ANDERSON. Mushroom Research Group, Erindale<br />

College, University <strong>of</strong> Toronto, Mississauga,<br />

Ontario, Canada L5L 1C6. Breeding behavior <strong>of</strong><br />

Agaricus species.<br />

Cultivated strains <strong>of</strong> Agaricus bisporus are, for the<br />

most part, genetically uniform. One goal <strong>of</strong> our research<br />

is to use wild populations <strong>of</strong> Agaricus as a<br />

source <strong>of</strong> genetic variability which can be transferred<br />

into the background <strong>of</strong> A. bisporus by forced somatic<br />

hybridization. From the increased range <strong>of</strong> inherited<br />

variability in hybrid cells or their derivatives,<br />

strains improved with respect to yield, shelf<br />

life, temperature optima for growth and fruiting, or<br />

any other parameter could be selected. Information<br />

on the mating systems <strong>of</strong> wild Agaricus spp. is a prerequisite<br />

to any breeding program. We have found,<br />

that, consistent with earlier reports, A. bitorquis<br />

is unifactorially heterothallic, with multiple<br />

alleles at the mating-type locus. Although nuclear<br />

migration was previously unknown in Agaricus, we<br />

found a strain <strong>of</strong> A. bitorquis whose nuclei apparently<br />

migrate within the opposing mycelium <strong>of</strong> some compatible<br />

mates. A. vaporarius, which is very closely<br />

related to A. bisporus, was also unifactorially<br />

hrterothallic. Further, A. bisporus, -and A.<br />

bitorquis, and A. vaporariuswere intersterile wiTh<br />

one another. The mating systems <strong>of</strong> several other<br />

species, A. silvicola, A. campestris. A. placomyces,<br />

and A. arvensis -yere not clear. I w~li describe the<br />

use <strong>of</strong> auxotrophic and drug-resistance aucations as<br />

markers for selec~ion <strong>of</strong> interspecies h~!terokoryons<br />

in pairings <strong>of</strong> intact, living mycelia ~nd in fusions<br />

<strong>of</strong> protoplasts and I will discuss the DKOSDeCtS<br />

. .<br />

<strong>of</strong><br />

- -<br />

overcoming intersterility barriers in Agaricus for<br />

breeding purposes.<br />

Anderson, R. C., see Liberta, A. E.<br />

Antonopoulos, A. A., see Wene, E. G.<br />

A.A. ANTONOPOULOS and E.G. WENE, Argonne National Laboratory,<br />

Energy and Environmental Systems, 9700 South<br />

Cass Ave., Argonne, IL 60439. Mutagenesis studies on<br />

Fusariwn oxyspom isolates.<br />

Selected Ftlsariwn strains have been studied to determine<br />

their potential for ethanol production from the<br />

decomposition and fermentation <strong>of</strong> biomass. In addition<br />

to screening strains isolated from natural habitats,<br />

new strains have been developed through W-<br />

irradiation <strong>of</strong> microconidia. In several cases W-<br />

mutants were more effective glucose and xylose fermenters<br />

and cellulase enzyme producers than the parental<br />

strains. Methodology and the results <strong>of</strong> mutagenesis<br />

efforts will be discussed.<br />

Arnott, H. J., see Whitney, K. D.<br />

Austin, W. L., see Wilfred, A., et. a1 .<br />

C. W. BACON and D. M. EINTON. Toxicology and<br />

Biological Constituents Research Unit, Russell<br />

Research Center, USDAIARS, Athens, GA 30613.<br />

Efficacy <strong>of</strong> Iodonitrotetrazolium violet for<br />

determining endophyte infected tall fescue seeds.<br />

A rapid and simple spectrophotometric method <strong>of</strong><br />

measuring the infection and viability <strong>of</strong> the fungal<br />

endophyte, Acremonium sp., in seed <strong>of</strong> tall fescue is<br />

presented and partially characterized. The assay is<br />

based on the reduction <strong>of</strong> a tetrazolium salt,<br />

2-(p-iodopheny1)-3-(p-nitropheny1)-5-phenyl<br />

tetrazolium chloride (INTI, by whole seed in the<br />

presence <strong>of</strong> nitrogen and Triton X-100. The method<br />

depends upon dehydrogenase enzyme activity to reduce<br />

the colorless INT into a violet-red compound<br />

(formazan) which is made water soluble by the Triton<br />

X-100. The procedure can be completed in a 24 to 48<br />

h period; the INT-formazan product is measured at<br />

490 nm, and the infection status <strong>of</strong> the seed lot<br />

assessed. The simplicity and rapidity <strong>of</strong> this<br />

method have many advantages over previously used<br />

methods (Eliza, seed growth, and microscopy) that<br />

are either complex, long andlor cannot distinguish<br />

living from dead fungi in seed. Several inhibitors<br />

and substrates <strong>of</strong> the electron transport system were<br />

used to determine the site <strong>of</strong> INT reduction in<br />

noninfected seed and contrasted with the apparent<br />

absence under anaerobic conditions in infected seed.<br />

E. R. BADHAM. Carolina Fungi, Inc. 2736<br />

Lakeview Dr., Raleigh, NC 27609. The influence <strong>of</strong><br />

humidity upon transpiration and growth in the mushroom<br />

Psilocybe cubensis.<br />

The influence <strong>of</strong> humidity upon individual<br />

basidiocarps <strong>of</strong> Psilocybe cubensis was studied using<br />

an environmentally controlled wind tunnel and a computer<br />

program which helped to model growth and


development. Regression models were developed which<br />

were able to explain 77% <strong>of</strong> the variation in the<br />

transpiration rate and 68% <strong>of</strong> the variation in growth<br />

rate. Transpiration and growth <strong>of</strong> this mushroom were<br />

significantly correlated with the humidity <strong>of</strong> the air.<br />

The fastest growth and the lowest transpiration<br />

occurred at the highest humidities. No inhibition <strong>of</strong><br />

growth was detected at 0 pascals VDD (100% RH).<br />

Misting accelerated growth and transpiration while<br />

light had no effect. Although humidity was a very<br />

important factor influencing transpiration and growth,<br />

the size and shape <strong>of</strong> the mushroom were also important<br />

in water relations. The final water content <strong>of</strong><br />

basidiocarps with thin stipes or those with large<br />

surface area/volume ratios was significantly lower<br />

than that <strong>of</strong> thick stiped mushrooms or those with<br />

small surface area/volume ratios even though humidity<br />

was equal. Growth rates under conditions which<br />

promoted the highest levels <strong>of</strong> hydration <strong>of</strong> the<br />

basidiocarp were rapid (up to estimated 4% increase<br />

in dry weight per hour).<br />

Barro, S. C., see Dunn, P. H., et. al.<br />

Barstow, W. E., see Freshour, G. D., et. al.<br />

- W.E. - BARSTOW, W.L. LINGLE and G.D. FRESHOUR.<br />

Botany Department, The Uni versi ty <strong>of</strong><br />

Georgia, Athens, GA 30602. The association<br />

<strong>of</strong> tubular and rough ER with gamma particle<br />

proteins in Blastocladiella emersonii ,<br />

Blastocladiella bri tannica, m a r i a<br />

anguillulae.<br />

The presporulation coenocytic thallus <strong>of</strong> B.<br />

emersonii, E.britannica and<br />

characterized by the<br />

~~~<br />

bundles' <strong>of</strong> tubular elements which ramify<br />

through the cytoplasm. The individual<br />

tubules are composed <strong>of</strong> a single unit<br />

membrane averaging 8.7 nm in thickness. At<br />

this time each individual tubule is<br />

surrounded by an 80 to 100 nm ribosome-free<br />

zone. When the tubules occur in bundles<br />

there is a regular 100 to 150 nm center to<br />

center spacing which results in numerous<br />

hexagonal arrays as observed in cross<br />

section. During the early stages <strong>of</strong><br />

zoosporangium formation the bundles <strong>of</strong><br />

tubules lose their ordered re1 ationship to<br />

each other and the previously clearly<br />

defined ri bosome-f ree area around each<br />

tubule becomes less distinct. At this time<br />

there is a rapid increase in rough ER and<br />

frequent connections are found between the<br />

tubules and cisternae <strong>of</strong> rough EH. The<br />

cisternae <strong>of</strong> rough ER contain the protein<br />

precursors <strong>of</strong> gamma particles. By the time<br />

<strong>of</strong> papilla formation the tubules had<br />

disappeared. We assume that the tubule<br />

membranes had been converted to rough EK.<br />

L. R. BATRA. U. S. Dept. Agriculture, Beltsville<br />

Agricultural Research Center, Beltsville, Maryland<br />

20705. Deceit and corruption: Ericaceae blights<br />

caused by Monilinia spp. mimic host flowers and<br />

exploit pollinators as vectors.<br />

A group <strong>of</strong> Monilinia spp. invades diverse Ericaceae<br />

(1). One species,, M. vaccinii-corymbosi (Reade)<br />

Honey is polytrophic on Vaccinium corymbosum L. and<br />

its several related species. In contrast, most other<br />

Monilinia spp. on the Ericaceae are rather species<br />

specific. They cause' a blight <strong>of</strong> nascent spring<br />

17<br />

shoots and mummification <strong>of</strong> fruit, e.g. the "mummy<br />

berry" stage in blueberries, cranberries (Vaccinium)<br />

and huckelberries (Gaylussacia). Recently we reported<br />

a new and unusual mechanism for dispersal <strong>of</strong> these<br />

pathogens where infected shoots, including leaves<br />

mimic flowers (2). The pathogen elicits behavior <strong>of</strong><br />

particular insect pollinators so that they are<br />

attracted to infected parts where they lick the<br />

mantle <strong>of</strong> conidia, and become contaminated with<br />

spores. When these insects subsequently visit host<br />

flowers, the conidia are deposited on their stigmas,<br />

resulting in infected ovaries; and other floral<br />

parts, to be further dispersed. Here I discuss<br />

significance <strong>of</strong> comingling <strong>of</strong> inocula <strong>of</strong> several<br />

sympatric Monilinia spp.: M. azaleae Honey, M.<br />

baccarum (SchrBt.) Whet. , g. megalospora (Wor.)<br />

Whet., fi. oxycocci (Wor.) Honey, M. polycodii<br />

(Reade) Honey, 1. vaccinii-corymbosi and others.<br />

At least one pair <strong>of</strong> Monilinia spp. hybridizes.<br />

1. Batra, L. R. 1983. Mycologia 75: 131-152.<br />

2. Batra, L. R. and S. W. T. Batra. <strong>1985</strong>.<br />

Science 226 (May issue).<br />

Beattie, S. W., see Hammill, T. M., et. al., a.<br />

Beattie, S. W., see Hammill, T. Y., et. al., b.<br />

- G. - L. BENNY J. L. .GIBSON, and J. W. KIMBROUGH.<br />

-9<br />

Department <strong>of</strong> Botany, University <strong>of</strong> Florida,<br />

Gainesville, FL 32611.<br />

Cytochemical observations on the merosporangia,<br />

merosporangiospores, and pseudophial ides <strong>of</strong><br />

Linderina pennispora.<br />

Young Linderina pennispora merosporangiospores<br />

have several discernible layers and spines<br />

embedded in their walls. Fewer layers are<br />

produced in the walls <strong>of</strong> the subtending<br />

pseudophialides, but the septum and an associated<br />

lobate structure (the abscission vacuole or<br />

labyrinthiform organelle) are chemically different<br />

than the other walls. Cytochemical studies<br />

revealed the presence <strong>of</strong> a glucose- or<br />

mannose-containing cell coat on the merosporangia.<br />

The wall <strong>of</strong> the merosporangium and<br />

merosporangiospore, and the neck <strong>of</strong> the<br />

pseudophialide are chemically different from the<br />

remainder <strong>of</strong> the wall <strong>of</strong> the pseudophialide or the<br />

labyrinthiform organelle. Polysaccharides appear<br />

to be present in the wall <strong>of</strong> the merosporangium,<br />

the spore spines, and the lenticular cavity.<br />

D. A. BETTERLEY. Spawn Mate, Inc., 555 North<br />

First St., San Jose, CA 95112.<br />

Biological control <strong>of</strong> pathogens <strong>of</strong><br />

cultivated mushrooms (Agaricus spp.).<br />

This paper serves as a brief review <strong>of</strong> biological<br />

control attempts in mushroom cultivation<br />

and discussion <strong>of</strong> recent progress in<br />

the isolation and introduction <strong>of</strong> microbial<br />

antagonists to reduce disease incidence. In<br />

most cases, the antagonist must colonize the<br />

compost and/or casing materials in the<br />

presence <strong>of</strong> pesticides or conditions used to<br />

control other pathogens.<br />

Sciarid flies (Lycoriella spp.:Diptera)<br />

have been effectively controlled in small<br />

scale trials using several systems, among<br />

them isolates <strong>of</strong> Erynia montana (Entomophthorales),<br />

nematodes parasitic to sciarid<br />

larvae, and Bacillus thuringiensis.


Nematodes, both parasitic and saprophytic,<br />

can cause yield reductions. Arthrobotrys<br />

species can be effective, although proper<br />

sanitation is a simpler remedy. Work is<br />

beginning on the control <strong>of</strong> Verticillium<br />

disease and bacterial mummy disease with the<br />

use <strong>of</strong> bacterial antagonists. The greatest<br />

success to date has been the control <strong>of</strong><br />

bacterial blotch disease with antagonistic<br />

strains <strong>of</strong> Pseudomonas fluorescens selected<br />

by Dr. Peter Fahy in Australia. Cooperative<br />

trials are underway in the U.S. for disease<br />

control in mushroom houses and also for<br />

increased postharvest quality <strong>of</strong> mushrooms.<br />

6. E. & H. V. T. COTiER. Department <strong>of</strong> Biology,<br />

Virginia Polytechnic Institute and State University,<br />

Blacksburg, VA 24061, U. S. A.<br />

Can sporocarp pattern measure the spatial pattern <strong>of</strong><br />

the vegetative mycelium? - A test using the bolete,<br />

Boletinellus merulioida.<br />

Ecological studies <strong>of</strong> higher fungi have depended on<br />

sporocarps as a measure <strong>of</strong> fungal presence,<br />

productivity, or dominance. A major criticism <strong>of</strong> these<br />

studies has been that the relationship <strong>of</strong> the<br />

sporocarps to the vegetative mycelium is unknown. The<br />

accuracy <strong>of</strong> a sporocarp-determined distribution pattern<br />

was tested by using sclerotia as a marker <strong>of</strong> the<br />

vegetative mycelium <strong>of</strong> Boletinellus rerulioidea. The<br />

spatial pattern <strong>of</strong> the vegetative mycelium was<br />

determined in 64 2 x 2 q contiguous quadrats and was<br />

compared to the spatial pattern <strong>of</strong> sporocarps produced<br />

in the quadrats over a 4-year period. Year-to-year<br />

sporocarp frequency in the quadrats varied greatly, and<br />

and sporocarp frequency for a single year was an<br />

unreliable indication <strong>of</strong> the pattern <strong>of</strong> the vegetative<br />

mycelium. However, cumulative sporocarp frequency over<br />

the 4-year period provided a good estimate <strong>of</strong> the<br />

spatial pattern <strong>of</strong> the mycelium. Sporocarp and<br />

sclerotial densities were centered around and declined<br />

outward from Fraxinus americam trees. In a nearby,<br />

second set <strong>of</strong> contiguous quadrats, no sporocarps were<br />

observed over the four years; neither were sclerotia<br />

present in the plot despite the presence <strong>of</strong> E.<br />

emeric-. The relationship between B. peruliow and<br />

E. meric- is also discussed.<br />

MEREDITH BLACKWELL, ANTHONY J. KINNEY, PAUL T.<br />

RADFORD, and CATHERINE M. DUGAS. Department <strong>of</strong><br />

Botany, Louisiana State University, Baton Rouge,<br />

Louisiana 70803, and R. L. GILBERTSON. Department<br />

<strong>of</strong> Plant Pathology, University <strong>of</strong> Arizona, Tucson,<br />

Arizona 85721. The chemical basis <strong>of</strong> Melzer's<br />

reaction.<br />

For the last hundred years mycologists have used<br />

Melzer's reaction as a taxonomic character. Two<br />

previous studies attribute the blue staining<br />

(amyloid) reaction to the presence <strong>of</strong> amylose in<br />

five species <strong>of</strong> Basidiomycetes. We have verified<br />

the presence <strong>of</strong> amylose and a correlated amyloid<br />

reaction in additional species <strong>of</strong> Basidiomycetes<br />

and in an ascomycete. Amylose and amylopectin were<br />

not detected in species which showed a red<br />

(dextrinoid) reaction. Species with a dextrinoid<br />

reaction did appear to have high concentrations <strong>of</strong><br />

certain quarternary ammonium compounds (QACs),<br />

which are known to form a red periodide complex<br />

with KI The QACs were measured quantitatively,<br />

after &A extraction <strong>of</strong> the fungus, by a<br />

spectrophotometric technique. They were tentatively<br />

identified as choline and glycine betaine by a<br />

combination <strong>of</strong> ion-exchange chromatography and<br />

2-dimensional thin layer chromatography. Con-<br />

firmation <strong>of</strong> this identification is at present<br />

being sought utilizing mass spectrometry. It is<br />

interesting to note that QAC accumulation,<br />

especially accumulation <strong>of</strong> glycine betaine, has<br />

been associated with salt and water stresses in<br />

angiosperms. QACs could be <strong>of</strong> ecological<br />

significance in fungi.<br />

MEREDITH BLACKWELL and G. MIKE W. ADAMS.<br />

Department <strong>of</strong> Botany, Louisiana State University,<br />

Baton Rouge, Louisiana 70803. The exudate <strong>of</strong><br />

Inonotus dryadeus.<br />

Inonotus dryadeus is a common root parasite <strong>of</strong><br />

hardwoods in the Gulf Coast region. Basidiocarp<br />

development is characterized by the transport <strong>of</strong> a<br />

watery exudate to the maturing basidiocarp surface.<br />

As much as 5 ml <strong>of</strong> exudate can be transported in 12<br />

hrs. While the mechanism <strong>of</strong> transport is<br />

uncertain, it is known that the exudate moves in<br />

thick-walled hyphae which lack cytoplasm and<br />

contain few septa; these hyphae end 1-2 mm from the<br />

basidiocarp surface. Cytoplasm is restricted to<br />

thin-walled hyphae which extend to the margin <strong>of</strong><br />

the basidiocarp. Similar transport hyphae are also<br />

present in Laetiporus sulphureus, d. persicinus,<br />

and other polypores which produce exudates.<br />

Exudate <strong>of</strong> i. dtiadeus from both living and dead<br />

trees <strong>of</strong> different species in characterized by low<br />

pH, high organic salt content, several free amino<br />

acids in low concentrations, and a variety <strong>of</strong><br />

unidentified proteins. The unconcentrated exudate<br />

has antibiotic activity at room temperature against<br />

all gram positive bacteria tested as well as<br />

Pseudomonas aeru~inosa. Activity is confined to a<br />

heat stable, low (


JEAN R. BOISE. The New York Botanical Garden,<br />

Bronx, NY 10458. A traditional fungal taxonomist<br />

tries cladistics.<br />

Resting aporea were eeparate, not organized into a<br />

cyetoeorue: they were ruet brown in color, amooth<br />

walled, and were 4-4.6 pa in diameter.<br />

19<br />

Cladistic methodology is employed to avail a fresh<br />

perspective on the taxonomy <strong>of</strong> the melanommataceous<br />

species named in Trematosphaeria. Congruence<br />

testing supports disposition <strong>of</strong> the taxa in a manner<br />

similar to that arrived at by traditional analysis.<br />

Outgroup comparison, using the Lophiostomataceae,<br />

provides evidence to reject the proposal that<br />

Trematosphaeria is a synonym <strong>of</strong> Melanomma, but more<br />

detailed statements about species placement are<br />

severely limited by the lack <strong>of</strong> studies on intrafamilial<br />

relationships in the outgroup and by the<br />

high degree <strong>of</strong> parallelism that is accepted in the<br />

taxonomy <strong>of</strong> the two families.<br />

Boucias, 0. G., see Pendland, J. C.<br />

S.M. BOYETCHKO and J.P. Tewari. Department <strong>of</strong> Plant<br />

Science, University <strong>of</strong> Alberta, Edmonton, Alberta,<br />

Canada T6G 2P5. A new Glomus with dimorphic<br />

chlamydospores.<br />

A previously unknown species <strong>of</strong> Glomus mycorrhizal<br />

with barley in Alberta was isolated.The proposed<br />

new species, Glomus dimorphicum sp. nov. is<br />

dimorphic, poTETTng both single (130 - 300 pm in<br />

diameter) and grouped chlamydospores (50 - 130 pm in<br />

diameter). The young single spores possess three<br />

wall layers: an outer hyaline wall layer which<br />

eventually sloughs <strong>of</strong>f, a middle laminated layer and<br />

a thin inner wall layer. Older spores <strong>of</strong> the single<br />

type lack the outer hyaline wall layer. The spores<br />

<strong>of</strong> the grouped type form discrete radiate<br />

clusters. The wall layers in these grouped spores<br />

are similar to those <strong>of</strong> the older single spore in<br />

having two wall layers. The spores <strong>of</strong>ten have soil<br />

particles agglutinated to their wall surfaces which<br />

makes study <strong>of</strong> the spore surface difficult. X-ray<br />

energy dispersive analyses facilitated the<br />

identification <strong>of</strong> the relatively clean areas <strong>of</strong> the<br />

outer hyaline wall layer. Examination <strong>of</strong> the roots<br />

<strong>of</strong> barley has revealed extensive hyphal<br />

colonization, very few vesicles and no arbuscul es.<br />

J. P. BRASELTON. Department <strong>of</strong> Botany, Ohio<br />

Univereity, Athene, OH 45701.<br />

Ultraatructure <strong>of</strong> Plaemodio~hora di~lantherae, A<br />

Plaamodiophoromycete Parasite on the Shoal Graaa.<br />

- ---<br />

Halodule wriahtii<br />

Plaemodio~hora di~lantherae (Ferdinandaen et<br />

Winge) Cook infected shoal graee, Halodule<br />

wriahtii Aecheraon, collected from the Indian<br />

River in Florida. In actively growing ehoota, color.<br />

<strong>of</strong> galla were white to light creaa near the shoot apex<br />

but light to dark brown beginning three to five nodea<br />

from the apex. The paraeite wae contained within the<br />

inner cortex, infected celle <strong>of</strong> which were enlarged to<br />

ee much aa 250 pm in maximum diameter. All etagee <strong>of</strong><br />

development appeared to be <strong>of</strong> the cyetogenoua phaae:<br />

no eporangie were obaerved. Ultraatructurally P.<br />

di~lantherae had eeveral feature8 coneietent with<br />

cystogenoue plasmodia <strong>of</strong> other Plaemodiophoromycetee:<br />

Plaemodia occurred within cytoplaaa <strong>of</strong> hoet celle,<br />

centrioles were paired end-to-end, and aynaptonemal<br />

coaplexee (SCe) occurred in nuclei <strong>of</strong> transitional<br />

plasmodia. The haploid chromosome number a8<br />

determined by counting the SCa wae nine, the loweet<br />

haploid number reported for Plaaaodiophoromycetee.<br />

Brewer, C., see Iturriaga, T.<br />

S.A. BRUNT and J.C. SILVER. Department <strong>of</strong><br />

Microbiology. University <strong>of</strong> Toronto, West Hill,<br />

Ontario, Canada, MlClA4. The effect <strong>of</strong> the steroid<br />

hormone antheridiol on secreted proteins in the fungus<br />

Achlya ambisexualis.<br />

The steroid hormone antheridiol induced changes in<br />

proteins in the secreted fraction <strong>of</strong> the fungus<br />

Achlya 'ambisexualis. When the 35~-labeled proteins<br />

from control and hormone-treated cells were analyzed<br />

using SDS polyacrylamide gel electrophoresis and<br />

fluorography both qualitative and quantitative changes<br />

were observed. The most prominent proteins observed<br />

in the secreted protein fraction from control cells<br />

had molecular weights <strong>of</strong> 57,000 (57K), 54,000 (54K)<br />

and 50,000 (50K) respectively. Con A affinity<br />

chromotography and treatment with the enzyme Endoglycosidase<br />

H strongly suggested that the latter two<br />

proteins were glycoproteins. After hormone treatment<br />

the 54K and 50K proteins were barely detectable but<br />

there was nearly a two-fold increase in the<br />

accumulation <strong>of</strong> a doublet <strong>of</strong> prominently labeled<br />

proteins with relative molecular weights <strong>of</strong> 44,400<br />

(44.4K) and 43,000 (43K) respectively. Neither <strong>of</strong><br />

these two proteins bound to a Con A column or were<br />

sensitive to enzymatic cleavage with Endoglycosidase<br />

H. Cleavage <strong>of</strong> the 54K and 50K proteins from control<br />

cells with Endoglycosidase H produced a 45K protein<br />

which migrated close to the 44.4K and 43K protein<br />

doublet from hormone-treated cells. These<br />

observations suggest that the steroid hormone<br />

antheridiol may induce changes in glycoprotein<br />

processing <strong>of</strong> secreted proteins in Achlya.<br />

(Supported by NSERC, Canada)<br />

Bunderson, C. V., see Weber, D. J., et. al.<br />

Sunderson, E. O., see Weber, D. J., et. al.<br />

L. M. CARRIS, D. A. GLAWE, and L. I?. GRAY. Dept. <strong>of</strong><br />

Plant Pathology, and USDA-ARS, Univ. <strong>of</strong> Illinois,<br />

Urbana, IL 61801. Isdlation <strong>of</strong> fungal pathogens <strong>of</strong><br />

soybeans from cysts <strong>of</strong> Heterodera glycines in<br />

Illinois.<br />

Cysts <strong>of</strong> Heterodera glycines, the soybean cyst nematode,<br />

were collected 1983-1984 from soybean fields in<br />

Illinois. Of over 50 species <strong>of</strong> fungi isolated from<br />

cysts, three were identified as known soybean pathogens.<br />

Identification <strong>of</strong> Corynespora cassiicola and<br />

Phialophora gregata, causal agents <strong>of</strong> Target Spot and<br />

Brown Stem Rot diseases, respectively, was confirmed<br />

by demonstrating their pathogenicity on 'Century'<br />

soybeans. Neocosmospora vasinfecta, causal agent <strong>of</strong><br />

Neocosmospora Stem Rot, was identified on the basis<br />

<strong>of</strong> morphological and cultural characters. This is<br />

the first report <strong>of</strong> C. cassiicola and N. vasinfecta<br />

from soybean fields in Illinois.<br />

MICHAEL A. CASTELLANO and R. MOLINA Forestry<br />

Sciences Laboatory, Pacific Northwest Forest and<br />

Range Experiment Station, Corvallis, OR 97331.<br />

Distribution, ecology and mycorrhizal potential <strong>of</strong><br />

some Pacific Northwest fungi.<br />

Mycorrhizae have been synthesized in pure culture


20<br />

for the first time with hypogeous Basidiomycota in<br />

the genera Alpova, Cautieria, Leucogaster,<br />

Leucophleps, Mycolevis, Radiigera and Ascomycotina<br />

in the genus Ceopora. These combinations gave<br />

positive results: Alpova trappei Fogel with<br />

Douglas-f ir, lodgepole pine, and Sitka spruce ;<br />

Gautieria monticola Harkn. and g. crispa Stewart L<br />

Trappe with lodgepole pine and Douglas-fir or Sitka<br />

spruce, respectively; Cautieria otthii Trog. with<br />

lodgepole pine and Sitka spruce; Geopora cooperi<br />

Harkn. and Leucogaster rubescens Zeller h Dodge<br />

only with Douglas-fir; Leucophleps spinispora Fogel<br />

and Mycolevis Sicci~leba Smith with Douglas-fir,<br />

~p ~-<br />

lodgepole pine, ponderosa pine, and western<br />

hemlock; Radiigera fuscoaleba Zeller only with<br />

western hemlock. In addition, Boletus mirabilis<br />

Murr., a lignicolous agaric, and Lycoperdon<br />

pyriforme Pers., a <strong>of</strong>ten lignicolous true puffball,<br />

formed mycorrhizae with western hemlock. The<br />

relationship <strong>of</strong> these results to the ecology <strong>of</strong><br />

these taxa is discussed.<br />

Cavender, J. C., see Hammer C. A.<br />

T.E. CHASE and R.C. ULLRICH. Botany Dept., University<br />

-- <strong>of</strong> Vermont, Burlington, VT 05405. Genetics <strong>of</strong> intersterility<br />

in Heterobasidion annosum.<br />

Our mating studies using a world-wide collection <strong>of</strong><br />

strains <strong>of</strong> this root-rotting basidiomycete provide<br />

data on the genetic system determining intersterile<br />

groups (i.e., biological, species). We have identified<br />

five intersterility (IS) genes. The IS genes and alleles<br />

are designated: VI+/Vl-, Vz+/VZ-, V3+/V3-, St/<br />

S-, and P+/P-. To be interfertile, two homokaryons<br />

must each carry a + allele for the same IS gene (e.g.,<br />

in the case <strong>of</strong> V1+ VZ- V3- S+ P- x Vl- V2- L13+ S+ P-<br />

the two are interfertile by virtue <strong>of</strong> St. Homozygosity<br />

for the positive alleles <strong>of</strong> any IS gene suffices<br />

and negative alleles do not affect the positive interaction.<br />

These IS genes function to determine intersterility<br />

and interfertility independently <strong>of</strong> incompatibility<br />

(i.e., mating type) alleles. Therefore,<br />

within interfertile groups, compatible homokaryons<br />

must be heterozygous for incompatibility alleles<br />

(e.g., A1 x A?). Many <strong>of</strong> the first isolates studied<br />

from nature carry - alleles for all V genes and are<br />

either S+/P- or S-/P+. Consequently, the IS' and 'PI<br />

intersterile groups were recognized first. The V<br />

genes were implicated subsequently when samples were<br />

increased. Our conclusions are based on analyses <strong>of</strong><br />

crosses involving progeny from naturally-occurring<br />

isolates and interfertile crosses. These data provide<br />

the first model for the genetic basis <strong>of</strong> intersterility<br />

and speciation in higher fungi.<br />

Choi, H. T., see Ross, I. K., et. al.<br />

Chung, W. C., see Setliff, E. C.<br />

W. G. CIBULA and C. L. OVREBO. Earth Resources Laboratory,<br />

NASA, NSTL Station, MS 39529 and Matthaei<br />

Botanical Gardens, The University <strong>of</strong> Michigan, Ann<br />

Arbor, MI 48105. Diversity and distribution <strong>of</strong><br />

mycorrhizal basidiomycetes in two Pinus taeda plots<br />

in Mississippi.<br />

Mycorrhizal basidiomycetes were inventoried in 2<br />

plots <strong>of</strong> Pinus taeda on a weekly basis in 1974-1975,<br />

1975-76 and 1983-84. The 120 x 120 foot plots have<br />

25 year old trees at 10 foot spacings, resulting in<br />

144 subplots. The two plots differ with seedlings<br />

<strong>of</strong> one having received a single dose <strong>of</strong> N-P-K<br />

fertilizer at the age <strong>of</strong> one year. The total wood<br />

volume today in the fertilized plot is twice that<br />

<strong>of</strong> the unfertilized plot. A greater diversity <strong>of</strong><br />

fungi and a greater number <strong>of</strong> sporophores occurred in<br />

the fertilized plot during each sampling period.<br />

Collection data from each subplot have been entered<br />

into a computer in such a manner that the spatial<br />

distribution <strong>of</strong> sporophore production for each<br />

species on each collectiondate, along with seasonal<br />

or yearly sums, has been preserved. These sum files<br />

were subjected to various statistical tests, such as<br />

the Pearson r correlation coefficient, for further<br />

analysis. Species showing good spatial correlations<br />

between seasons include Cortinarius semisanguineus,<br />

Suillus decipiens and Tricholoma flavovirens.<br />

Also,.an algorithm has been developed to calculate<br />

the relationship between the species in a specific<br />

subplot with all other species within the subplot.<br />

Differences in aircraft radiometric remote sensor<br />

values between 0.4 & 2.5 pm correlate well with the<br />

differences in mycorrhizal involvement demonstrated<br />

by the observed field data.<br />

W. G. CIBULA, D. P. LEWIS and N. S. WEBER.<br />

m~r/~RL,at'l. Space Tech. Lab., NSTL, MS<br />

39529; Temple-Eastex, Evadale TX 77615;<br />

Herbarium, Univ. <strong>of</strong> Mich., Ann Arbor, MI<br />

48109. Observations on the boletes <strong>of</strong> the<br />

Gulf Coast region.<br />

The diversity <strong>of</strong> boletes in southeastern<br />

North <strong>America</strong> is perhaps the greatest on the<br />

continent. These mycorrhizal fungi include a<br />

number <strong>of</strong> species which are seldom<br />

encountered in other regions <strong>of</strong> North<br />

<strong>America</strong>. Some elements <strong>of</strong> the bolete flora<br />

such as Boletellus ananus occur elsewhere in<br />

tropical regions, particularly the Asian<br />

tropics. Other species such as Boletus<br />

catervatus, described from the Asian tropics,<br />

have been found on the Gulf Coast. Species<br />

diversity in Suillus and Leccinum appears to<br />

be lower in the Coastal Plain than elswhere<br />

in North <strong>America</strong> while that <strong>of</strong> Tylopilus,<br />

Strobilomyces, and Boletus seems to be<br />

greater.<br />

Clark, J., see Hu, F.-S, et. al. -<br />

Clark, J., see Hu, F.-S.<br />

- K.W. OOCHRAN. Departments <strong>of</strong> Epidemiology and <strong>of</strong><br />

~rmacology, University <strong>of</strong> Michigan, Ann Arbor, M I<br />

48109, and NAMA Committee. Cases reported to the<br />

NAMA Mushroan Poisoning Case Registry in 1984.<br />

In 1984 the Registry received 61 reports involving<br />

87 cases, sane involving earlier events. Most cases<br />

(87%) involved mushrcuns ingested for fccd; 8% for<br />

non-nutritional recreation; 5% accidently by<br />

children Eight cases involved unknown s~ecies: 6<br />

cases, mixed species - all Amanita. ~hlo~o~hyllun<br />

mol Mites was the most frequently reported species<br />

&followed<br />

by Annillaria mellea, 6; mnita<br />

pantherina and Collybia acervata, 4; Amanita<br />

muscaria and Leucoagaricus naucinus, 3. TWO fatal<br />

cases involved Amanita bisporigera and Psi locybe<br />

cubensis, the latter anaphylactically. With the<br />

newly reported cases, 2 or more incidents have now<br />

been reported to the Registry for the following<br />

species (syrnptams for all were gastrointestinal and<br />

as noted): Amanita muscaria, 5 -2 with very viscous<br />

mucus, 1 each ha1 lucination and unconscious; A.<br />

virosa 4; millaria mellea, 6; Collybia acervatya<br />

-I


4-a 11 severe GI; Cratere llus cornucopioides, 2;<br />

Galerina autumnalis, 2 - severe GI; Lactarius<br />

chelidonius, 2; Leumagarias naucinus, 4; Lepiota<br />

-<br />

rubrotincta, 2; Phaeolepiota aurea, 2f Pleurotus<br />

ostreatus, 2; Psilocybe plbensis. 2 muscle tremors<br />

and CNS; Russula & 3ental is, 2; Scleroderma<br />

citrinum, 2. More extensive reporting <strong>of</strong> cases,<br />

where pr<strong>of</strong>essiona 1 or amateur mycologists are<br />

involved, is needed.<br />

S. D. COHEN and J. J. MOTTA. Department <strong>of</strong> Botany,<br />

University <strong>of</strong> Maryland, College Park, MD 20742.<br />

Associated protein changes with rhizomorph differentiation<br />

in Armillaria mellea.<br />

Molecular events associated with the differentiation<br />

<strong>of</strong> rhizomorphs on undifferentiated mycelium <strong>of</strong><br />

Armillaria mellea have not been studied previously.<br />

Undifferentiated mycelium is induced to differentiate<br />

rhizomorphs in a minimal medium containing minute<br />

amounts <strong>of</strong> alcohol. This transformation is accomplished<br />

in four distinct stages; induction, initiat<br />

ion, differentiation and rhizomorph elongat ion.<br />

Inhibitor studies with cycloheximide and actinomycin<br />

D indicate that rhizomorph differentiation is regulated<br />

at the transcriptional level. Quantitative<br />

differences exist between induced and non-induced<br />

mycelia with respect to the total amount <strong>of</strong> protein.<br />

Protein extracts from induced and non-induced mycelia<br />

were analyzed by one-dimensional polyacrylamide gel<br />

electrophoresis. The number <strong>of</strong> peptides differed<br />

when induced and non-induced mycelia were coinpared.<br />

Cole. R. J., see Yates, I. E., et. al.<br />

J. C. Cooke Biology Group, University <strong>of</strong> Connecticut<br />

at Avery Point, Groton, CT 06340. VA mycorrhizal<br />

fungi associated with Amnophila breviligulata in a<br />

Connecticut sand dune.<br />

Recent studies on VA fungi associated with Ammophila<br />

breviligulata from marine sand dunes have shown a<br />

positive correlation between the percent cover <strong>of</strong><br />

the dune by Ammophila and VA fungal spores from<br />

rhizosphere samples. Spore density and spore species<br />

have been shown to increase with the age and stability<br />

<strong>of</strong> the dunes. Samples from a dune-beach area <strong>of</strong><br />

Bluff Point State Preserve in southeastern Connecticut<br />

have produced findings that support the results<br />

reported in other studies. The dune is a tombolo <strong>of</strong><br />

medium fine sand and is known as Bluff Point Beach<br />

and Bushy Point Beach. Samples were taken from the<br />

rhizosphere <strong>of</strong> Ammophila plants on three parallel<br />

transects at regular intervals. The transects were<br />

2 meters apart and crossed the dune from the south<br />

facing side on Fisher's Island Sound to the north<br />

facing side on the Poquonock River. A modified wetseiving<br />

procedure that emphasized counts <strong>of</strong> VA spores<br />

<strong>of</strong> Gigaspora larger than 0.27 mm was used. The<br />

results <strong>of</strong> the findings will be presented.<br />

Cooper, M. O., see Ellzey, J. T., et. al.<br />

Cotter, D. 4., see Harris, S. D.<br />

Cotter, H. V. T., see Bills, G. F.<br />

J.M. CURLIN, Department <strong>of</strong> Botany, University <strong>of</strong><br />

California, Davis, California 95616. Ultrastructural<br />

features <strong>of</strong> Microstroma juglandis:<br />

A taxonomic anomaly.<br />

Microstroma juglandis (Heterobasidiomycetes-<br />

Cryptobasidial El-a eaf parasite <strong>of</strong> several<br />

Juglans species. The life cycle includes a<br />

yeast phase but repetitive germination is<br />

unknown. The basidium, which is aseptate, bears<br />

8 or more symnetrical ly attached basidiospores<br />

on short, peg-like structures. In the process<br />

<strong>of</strong> conducting growth studies under various<br />

environmental conditions, it was observed that<br />

some isolates form hyphal strands in culture.<br />

Three fixation techniques have been compared in<br />

the preparation <strong>of</strong> this organism for electron<br />

microscopy, including the technique <strong>of</strong> freeze<br />

substitution. A study <strong>of</strong> the ul trastructrual<br />

features <strong>of</strong> this fragile organism <strong>of</strong>fers new<br />

data concerning the taxonomic position <strong>of</strong> this<br />

obscure pathogen.<br />

KURT R. DAHLRERG. Campbell Institute for<br />

Research and Technology. P.O. Box 311.<br />

Napoleon, OH 13545.<br />

AGARICUS SOMATIC CELL HYBRIDIZATION.<br />

The commercial mushroom fungus Agaricus<br />

bisporus (A. brunnescens) is generally<br />

considered to have limited genetic<br />

diversity. Extensive inbreeding <strong>of</strong><br />

commercial strains as well as the inherent<br />

difficulties associated with secondary<br />

homothallism have led researchers to<br />

believe that the upper l i m i t <strong>of</strong> strain<br />

improvement is being approached.<br />

One alternative to a traditional mushroom<br />

breeding program which may hold promise to<br />

increase genetic diversity and result in<br />

improved mushroom strains is interspecies<br />

hybridization. Recent efforts have<br />

attempted to create interspecies hybrids<br />

through protoplast fusion. Although this<br />

technique has proven to be quite<br />

successful among other fungal groups,<br />

methods to create, fuse, and regenerate<br />

Agaricus protoplasts are inefficient, and<br />

much additional research is needed.<br />

Research efforts by several groups to<br />

achieve successful fusion <strong>of</strong> Agaricus<br />

protoplasts and the advantages <strong>of</strong> using<br />

protoplast methodologies w i l l be reviewed<br />

and compared to previous attempts to<br />

create improved mushroom strains.<br />

Oashek, W. V., see Taylor, R., et. al.<br />

-- 6. DEML, Lehrstuhl Spezielle Botanik, Universitat<br />

Tubingen, Auf der Morgenstelle 1, D-7400 Tubingen,<br />

Fed. Rep. <strong>of</strong> Germany.<br />

Recent trends in the taxonomy <strong>of</strong> the phragmobasidial<br />

Ustilaginales.<br />

For a long time the smuts have been considered as a<br />

more or less uniform group <strong>of</strong> parasitic fungi. But<br />

in truth the term "smut fungi" describes rather a<br />

type <strong>of</strong> infection than a natural group <strong>of</strong> fungi.<br />

Quite recently the phragmobasidial Ustilaginales have<br />

been analized by modern techniques, such as enzymatic<br />

patterns, siderophore formation under low iron conditions,<br />

and sequences <strong>of</strong> 5s ribosomal RNA. As a<br />

result <strong>of</strong> these studies carried out on cultures it


-<br />

can be assumed that even the Ustilaginales s. str.<br />

seem not to represent a homogeneous taxon.<br />

On that basis a number <strong>of</strong> species <strong>of</strong> the genera<br />

Anthracoidea, Far sia, ~icrobotr~um, S hacelotheca<br />

soorisorium. ~- ~<br />

a&laao<br />

~<br />

were restu#kTGTiE;<br />

mbrphologicai characteristics and the germinat ion <strong>of</strong><br />

teliospores.<br />

In consideration <strong>of</strong> the host plants, the site and<br />

morphology <strong>of</strong> the sori, tel iospore formation and<br />

germination, as well as the criteria cited above, the<br />

phragmobasidial Ustilaginales can be divided into at<br />

least three clusters.<br />

1) Genera which parasitize monocotyledonous hosts,<br />

2) genera which parasiteze dicotyledonous hosts -<br />

these groups show an obvious affinity to the<br />

heterobasidiomycetous yeast genera Leucosporidium<br />

and Rhodos oridium -, and<br />

3) Far ria, aPgenus which is unique because <strong>of</strong> the<br />

&on <strong>of</strong> the tel iospores.<br />

Dorner, J. W., see Yates, I. E., et. al.<br />

Dugas, C. M., see Blackwell, M., et. al.<br />

Dunn, P. H., see Durall, 0. M.<br />

P. H. DUNN, S. C. BARRO, AND M. A. POTH. USDA Forest<br />

Service, Pacific Southwest Forest and Range Experiment<br />

Station, Forest Fire Laboratory, 4955 Canyon Crest Dr.,<br />

Riverside, CA 92507. Comparison <strong>of</strong> physiological<br />

methods to measure soil microbial biomass.<br />

Fungi generally account for three-fourths <strong>of</strong> the<br />

microbial biomass in soil. Two <strong>of</strong> the preferred<br />

physiological methods <strong>of</strong> measuring the total microbial<br />

biomass are the fumigation and incubation technique<br />

<strong>of</strong> Jenkinson and Powlson and the glucose addition<br />

technique <strong>of</strong> Anderson and Domsch. The glucose<br />

addition method gives potential biomass for a site<br />

while the fumigation technique gives a measure <strong>of</strong><br />

current biomass. The soil microbial biomass in a<br />

chaparral chronosequence (six separate sites) was<br />

evaluated with both methods using soil from beneath<br />

several Adenostoma fasciculatum (~f) and Ceanothus<br />

greggii (Cg) shrubs at each site. The two methods<br />

indicated similar trends in biomass fluctuation with<br />

stand age. Regression analysis showed that the two<br />

methods were directly related for both shrub species<br />

(Af: r= 0.85, Cg: r= 0.62, combined: r= 0.73).<br />

D. M. and P. H. WNN. Pacific Southwest<br />

Forest and mge Experiment Station, Forest Service,<br />

U. S. Department <strong>of</strong> Agriculture, Forest Fire Laboratory,<br />

4955 Canyon Crest Drive, Riverside, CA 92507.<br />

The use <strong>of</strong> an ultrasonic probe for renwing fungal<br />

spores from California bay ( m a r i a cal ifornica<br />

(H. & A.) Nutt.) leaves.<br />

Root, leaf, and soil washing techniques were developed<br />

to facilitate the isolation <strong>of</strong> fmgi present in the<br />

vegetative state rather than those in a transient<br />

spore state. These techniques have used shaking<br />

and txlbbling mechanics to remwe transient spores,<br />

leaving behind resident fmgi. The resident fmgi<br />

can then be isolated by plating leaf, root, and<br />

soil particles onto growing media. The washing<br />

efficiency <strong>of</strong> these methods has been low. In some<br />

studies, as many as 60 one-minute washings per sanple<br />

were required. In bacteriological research, an<br />

ultrasonic probe has been used to dislodge bacteria<br />

from soil. Ramval efficiency is higher than that<br />

achieved by shaking mechanics. Results <strong>of</strong> washing<br />

cal if ornia bay leaves and subsequent f ungal isolation<br />

confirm previous studies m bacteria. Ultrasonicaticm<br />

was fmd to be more efficient than shaking in the<br />

renwal <strong>of</strong> transient spores from leaves. Results<br />

from sampling waste water for viable transient spores<br />

indicated that the duration <strong>of</strong> washing and the<br />

anperage used with the probe must be adjusted to<br />

aquire maximm remwal efficiency, but at the saw<br />

time avoid injury to the transient spores and<br />

vegetative mycel im.<br />

M.J.DYKSTRA and E.J.NOGA. School <strong>of</strong> Veterinary<br />

Medicine, North Carol ina State University, Raleigh,<br />

NC 27606. A Newly Described Oomycete Disease <strong>of</strong><br />

Fish, Menhaden Ulcerative Mycosi s (MUM).<br />

In the spring, summer, and fall <strong>of</strong> 1984, deep skin<br />

ulcers were noted in a large proportion <strong>of</strong> menhaden<br />

collected from the estuaries <strong>of</strong> North Carolina. Wet<br />

mounts <strong>of</strong> lesion material showed broad, aseptate<br />

hyphae in 54 out <strong>of</strong> 56 lesions. Histopathology<br />

revealed broad, aseptate hyphae in 90% <strong>of</strong> the lesions<br />

to which the fish had mounted an immune response leading<br />

to large granulomas surrounding the hyphae. Lesion<br />

material from 39 fish was placed on nutrient media for<br />

14 hours at room temperature at which time emerging<br />

hyphal tips were removed to fresh media. Twelve <strong>of</strong><br />

the lesions contained Achls or Sa role nia sp., 13<br />

contained imperfect fuF, and 9$kXdk fungi.<br />

In some cases, hyphae were teased from the lesion.<br />

After 14 hours, the growing tips were transferred and<br />

Achly; sp. was subsequently identified. The intense<br />

granu omatous response to the fungus coupled with the<br />

absence <strong>of</strong> any other predominant parasites in the<br />

lesions suggests the deep involvement <strong>of</strong> the fungus<br />

with the disease. The ubiquity <strong>of</strong> the fungal genera<br />

involved further suggests that other environmental<br />

factors are the primary cause <strong>of</strong> the disease with the<br />

fungi being heavily involved in the lethal end-stage<br />

<strong>of</strong> the disease. It is particularly unusual to find<br />

Oomycetes in the high salinities (up to 1.3 ppt) from<br />

which the fish were collected.<br />

J. J. ELLIS. Northern Regional Research Center, ARS,<br />

USDA, Peoria, IL 61604. Species and varieties in the<br />

Rhizopus microsporus group as indicated by their DNA<br />

complementarity.<br />

Deoxyribonucleic acid renaturation studies between<br />

authenticated strains <strong>of</strong> Rhizopus species that f om<br />

short sporangiophores support conclusions that most<br />

<strong>of</strong> those published species should be considered<br />

varieties <strong>of</strong> R. microsporus.<br />

Strains <strong>of</strong> R. chinensis<br />

var . liquefaciens , ;: . pseudochinensis, R . oligosporus,<br />

R. cohnii, R. rhizopodiformis, and R. pygmaeus<br />

gave high nuclear DNA relatedness with strains <strong>of</strong> R.<br />

microsporus and R. chinensis. In contrast, strains<br />

<strong>of</strong> R. tritici and R. niveus showed low relatedness<br />

with R. microsporus and R . chinensis, but much higher<br />

relatedness with strains <strong>of</strong> R . arrhizus . Theref ore,<br />

nuclear DNA complementarity studies are consistent,<br />

for the most part, with conclusions recently based on<br />

morphological observations concerning varieties and<br />

species <strong>of</strong> Rhizopus .<br />

J. T. ELLZEY, M. 0. COOPER and T. H. HAMMONS.<br />

Biological Sciences, University <strong>of</strong> Texas at<br />

El Paso, El Paso, TX. 79968-0519. Ultrastructure<br />

<strong>of</strong> membrane-bounded structures<br />

within hypovirulent strains <strong>of</strong> Endothia<br />

(Cryphonectria) parasitica.<br />

Transmission electron microscopy <strong>of</strong> freezesubstituted<br />

hyphae <strong>of</strong> virulent and hypovirulent<br />

strains <strong>of</strong> Endothia (Cryph0nectria)para-


sitica has revealed the presence <strong>of</strong> aggregates<br />

<strong>of</strong> membrane-bounded structures (30-80nm<br />

in diam) within the hypovirulent and convert<br />

strains (113; 802 and 713). Such particles<br />

were not observed within the virulent strains<br />

(67 and 155). Utilizing a polyethylene glycol<br />

extraction procedure followed by negative<br />

staining with 0.5% uranyl acetate, two subpopulations<br />

<strong>of</strong> spherical particles (21-42 nm<br />

in diam) and (52-92 nm in diam) were obtained<br />

from the hypovirulent and convert strains.<br />

No such particles were isolated from the virulent<br />

strains. Diphenylamine, orcinol and e-<br />

thidium bromide tests are being conducted to<br />

determine if there is an association between<br />

nucleic acids and the membrane-bounded structures<br />

which were obtained from polyethylene<br />

glycol extractions <strong>of</strong> hyphae.<br />

--<br />

G.W. Erdos Dept. Micro. & Cell Sci. & C.M. West<br />

Dept. Anatomy, Univ. <strong>of</strong> Florida, Gainesville, FL<br />

32611. Use <strong>of</strong> monoclonal antibodies for the<br />

localization <strong>of</strong> carbohydrate in Dictyostelium.<br />

Glycoproteins (GP) that bind wheat germ agglutinin<br />

(WGA) are secreted into the medium during<br />

development in liquid. To determine which <strong>of</strong><br />

these became associated with the insoluble<br />

extracel lular matrix during normal development on<br />

a solid substratum, monoclonal antibodies were<br />

raised against cellular WGA binding glycoproteins.<br />

Three clones were chosen which produced anti bodies<br />

against distinct families <strong>of</strong> developmentally<br />

regulated GPs. The epitopes are carbohydrates<br />

since they are pronase resistant and periodate<br />

sensitive. Thin sections <strong>of</strong> 20 hr. culminants<br />

were labelled indirectly using an ammonium sulfate<br />

fraction <strong>of</strong> hybridoma culture supernatant followed<br />

by goat antimouse IgG bound to colloidal gold.<br />

Antibody 81.8 labelled the plasma membrane (PM) &<br />

internal vesicles <strong>of</strong> prespore & prestalk cells &<br />

the PM 81 central vacuole <strong>of</strong> stalk cells. Secreted<br />

epitopes <strong>of</strong> this anti body were incorporated into<br />

the slime sheath. Antibody 83.5 was prespore<br />

specific being localized on the PM & internally.<br />

Secreted GPs <strong>of</strong> this family were incorporated in<br />

the slime sheath & the stalk tube. Antibody 40<br />

labelled both prestalk cells & to a lesser extent<br />

prespore cells. This epitope was localized in the<br />

slime sheath only in the prespore area. Thoughts<br />

on methodologies for the preservation <strong>of</strong><br />

carbohydrate epitopes are also considered.<br />

R. C. EVANS and H. STEMPEN. Biology Department,Rutgers<br />

University, Camden, NJ 08102. Localization <strong>of</strong> protein<br />

in the hyphal sheath <strong>of</strong> Bipolaris maydis race T.<br />

Previous studies have demonstrated that thesheath-like<br />

extension <strong>of</strong> the cell wall found on germ tubes and hyphal<br />

tips <strong>of</strong> Bipolaris maydis race T contains antigenic<br />

material. Experiments utilizing rabbit IgG antiserum<br />

showed the ferritin label concentrated in discrete<br />

patches within the fibrillar matrix <strong>of</strong> the<br />

sheath and more evenly distributed on the outer surface<br />

<strong>of</strong> the hyphal wall proper. When germinated conidia<br />

were treated with papain there was a considerable<br />

reduction in the localization <strong>of</strong> the ferritin label in<br />

the sheath, indicating that the antigenic material is<br />

proteinaceous in nature. When germinated conidia were<br />

reacted with ~ odavue~ protein visualization reagents,<br />

darkly-staining patches could also be observed in the<br />

sheath using light microscopy. Prior treatment with<br />

papain reduced or eliminated this staining, lending<br />

support to the hypothesis that protein is localized in<br />

these regions. Previous studies have also shown that<br />

the sheath reacts with diaminobenzidine and hydrogen<br />

peroxide (DAB/H202) to form a dark product, and experiments<br />

were performed to determine if the protein component<br />

<strong>of</strong> the sheath has peroxidase activity. However,<br />

the DAB/H202 reaction product accumulates primarily in<br />

the fibrillar portion <strong>of</strong> the sheath, and the intensity<br />

<strong>of</strong> the reaction is not diminished by prior treatment<br />

with anti-Bipolaris antiserum nor heat. Thus, the<br />

proteinaceous patches in the sheath are not directly<br />

involved in the DAB/H202 reaction.<br />

D. F. FARR. Mycology Laboratory, Plant Protection<br />

Institute,U.S. Department <strong>of</strong> Agriculture,Beltsville<br />

Agricultural Research Center, Beltsville, Maryland<br />

20705. Ccmputerization <strong>of</strong> the National Fungus<br />

Collections.<br />

Over the last five years the Mycology Laboratory has<br />

successfiill~ implenazted a ~rojecto computerize<br />

the specimen label data in the National Fungus<br />

Collections. Currently about 220,000 specimens <strong>of</strong><br />

rusts, smuts, and polypores have been catalogued.<br />

OLn ex~eriences during the project's developent as<br />

well as our current procedures will be discussed. We<br />

have found that to a large extent the overall management<br />

<strong>of</strong> the project is wre brtant than the types<br />

<strong>of</strong> cquter hardware or s<strong>of</strong>tware. Factors that we<br />

have found critical to the success <strong>of</strong> the project,<br />

such as the addition <strong>of</strong> unique nunbers to each specimen,<br />

will be briefly discussed. Same general characteristics<br />

<strong>of</strong> the kinds and distributions <strong>of</strong> the<br />

specimens in the NFC will be ~resented. In addition<br />

to providing research scientists with listings <strong>of</strong><br />

various groups <strong>of</strong> f q i for their own studies, the<br />

data base is also being utilized in other ways such<br />

as the revision <strong>of</strong> the Index <strong>of</strong> Plant Diseases in<br />

the United States (USDA, Agriculture Handbook No.<br />

165) .<br />

'and 0. K. Miller Jr. Department <strong>of</strong> Biology,<br />

VPI & SU, Blacksburg, Va. 24061. A biosystematic study<br />

<strong>of</strong> the AGROCYBE PRAECOX species complex.<br />

Certain members <strong>of</strong> the genus AGROCYBE (Bolbitiaceae,<br />

Basidiomycetes) are highly polymorphic and form species<br />

complexes. As a result, considerable taxonomic<br />

confusion is associated with these groups <strong>of</strong> species.<br />

The A. PRAECOX species complex is the subject <strong>of</strong> this<br />

study. Biosystematic techniques have been employed to<br />

help define the range and limits <strong>of</strong> variation among<br />

taxa in this complex. This study focuses on mating<br />

compatibility and correlated morphological<br />

characteristics. Mating relationships <strong>of</strong> populations<br />

obtained from three disjunct geographic. regions<br />

(western North <strong>America</strong>, eastern North <strong>America</strong>, and<br />

western Europe) have been examined. Regional mating<br />

relationships were analysed by confronting two<br />

compatible single spore isolates per collection in<br />

every unique combination. Out <strong>of</strong> nine populations<br />

representing w. North <strong>America</strong>, two intersterile mating<br />

compatibility groups were identified. However, only one<br />

mating compatibility group was identified from nine<br />

populations representing e. North <strong>America</strong>. Two<br />

intersterility groups were identified from four<br />

collections representing w. Europe. Mating<br />

relationships among populations from the three<br />

geographic regions and their correlated morphological<br />

characteristics are compared and discussed.


24<br />

L. FREDERICK, IVAN L. ROTlI, and lXETER P E N D ~ ~ .<br />

Howard University, Washington, DC 20059, University <strong>of</strong><br />

Georgia, Athens, GA 30605, and U. S. Forest Service,<br />

Mge Tinter and Wildlife Division, Atlanta, GA 30309<br />

The "peridial platelets" <strong>of</strong> Clast&m<br />

cation.<br />

- a clarifi-<br />

Fuller, N. S., see Freshour, G. 0.. et. al.<br />

J.1:. GEMMA and R.E. KOSKE. Department <strong>of</strong> Botany,<br />

university <strong>of</strong> Rhode Island, Kingston, R. I. 02881.<br />

Seasonal Spore Dormancy in Gigaspor5 gigantea.<br />

Structures that have been described as "peridial<br />

platelets" =present the key diagnostic feature typifying<br />

the myxcmycete genus Clastodenra. Tnese discrete<br />

flattened structures that persist in sporangia<br />

<strong>of</strong> I17embers <strong>of</strong> the genus have been reported to be <strong>of</strong><br />

peridial origin. \Ve have investigated the nature <strong>of</strong><br />

these "peridial" platelets with scanning electron<br />

microscopy and have found them to be ontogenetically<br />

related to the capillitial system instead <strong>of</strong> being<br />

derived from the peridium. Platelets develop from<br />

the dichotcmised ends <strong>of</strong> capillitial branches that<br />

broaden into oval or elongate, flattened, anastarosed<br />

segrrents. They nray have a m t h to slightly pitted<br />

outer surface and smat veined undersurface. me<br />

platelets are relatively thick and the expanded portion<br />

has a clear uninterrupted continuity with the<br />

narm cvlindric ends <strong>of</strong> the ca~illitial branches.<br />

During the early stages <strong>of</strong> sporkgial develomnt the<br />

capillitial system and sporoplasm are enveloped by a<br />

thin &rano& peridium. When the sporangib<br />

matures the peridium disintegrates exposing the<br />

underlying cmillitial platelets and the spore mass.<br />

The only portion <strong>of</strong> the-peridium that persists in a<br />

nature sporangium is a collar-like mant at the top<br />

<strong>of</strong> the stalk.<br />

Frederick, L., see Howell-Major, Y., et. al.<br />

Frederick, L., see Wilfred, A., et. al.<br />

- G.D.FRESHOUR, -<br />

W.E.8ARSTUW and M.S.FULLER.<br />

Botany Department, The University <strong>of</strong><br />

Georgia, Athens, GA 30602. The<br />

ultrastructure <strong>of</strong> mitosis in Rhizidiomyces<br />

apophysatus.<br />

Serial sections <strong>of</strong> the early stages <strong>of</strong><br />

germination and <strong>of</strong> sporogenesi s in R.<br />

a o h satus revealed the following features<br />

(I) the angle between the<br />

centrioles <strong>of</strong> prophase nuclei is ca. 135'<br />

(2) the nuclear envelope persists and is<br />

fenestrated at the poles (3) the nucleolus<br />

disperses into a pocket to the sides <strong>of</strong> the<br />

metaphase chromosomes and is not seen at<br />

later stages (4) Golgi membranes and<br />

vesicles are abundant adjacent to the<br />

centrioles and polar fenestrae at prophase<br />

and metaphase (5) during metaphase vesicles<br />

move into the spindle apparatus and are<br />

found on either side <strong>of</strong> the metaphase<br />

chromosomes. At anaphase these i n t ranucl ear<br />

vesicles move ahead <strong>of</strong> the advancing<br />

chromosomes (6) perinuclear ER and<br />

microbodies surround the nuclei during<br />

anaphase and telophase (7) during telophase<br />

the daughter nuclei are formed by the<br />

addition <strong>of</strong> new envelope to existing<br />

membranes (8) the mid-region <strong>of</strong> the original<br />

nucleus is excluded at telophase. The<br />

morphological events <strong>of</strong> mitosis in K.<br />

apophysatus supports the taxonomic<br />

separation <strong>of</strong> the Hyphochytriomycota from<br />

the Oomycota and Chytridiomycota.<br />

Freshour, G. D., see Rarstow, W. E., et. al.<br />

Monthly field collections <strong>of</strong> Gigaspora gigantea<br />

demonstrated seasonal variation in spore number and<br />

percent spore germination. An increase in spore<br />

number in September was correlated with a reduction<br />

in percent germination that continued over a 2 month,<br />

period. Germination <strong>of</strong> spores on sand plates increased<br />

from 4.2% in September to 945 in December. This<br />

agrees with previously reported evidence for a spore<br />

dormancy period that was found for other vesicular<br />

arbuscular mycorrhizal (VAM) species grown in pot<br />

culture.<br />

R. V. GESSNER, R. I\'. SCIIUL:, :lnd bl. :A. RObLXYO.<br />

Department <strong>of</strong> Bio1ogic:ll Sciences, licstcrn I1 1 ino is<br />

University, blacomb, IL blJS5. Popul:~t ion gcnct ic<br />

analysis <strong>of</strong> blorchel la spp.<br />

Starch gel electrophoresis was utilized to investigate<br />

inheritance patterns and the population<br />

structure <strong>of</strong> blorcllella spp. from west centrill<br />

I1 1 inois. Twelve enzymes encoded by 16 presumpr ive<br />

loci were analyzed from tissue homogenotes <strong>of</strong> broth<br />

grown mycelium and field collected ascocarps. Data<br />

were analyzed to determine the extent <strong>of</strong> intrn- and<br />

inter-specific variation within and among populations.<br />

In order to determine the potential for gene flow<br />

between individuals, single iiscospore cultures from<br />

individual ascocnrps <strong>of</strong><br />

-<br />

M.<br />

--<br />

del iciosa were studied<br />

and preliminary data silggcst that the a1 1 eles<br />

segregate in a Hendel inn manner. Elect romorph<br />

differences were greater between M. ~leliciosa and<br />

-!I.<br />

csculenta than among individual isolates <strong>of</strong><br />

either species. These data support the division <strong>of</strong><br />

these taxa into separate species.<br />

- J. L. GIBSON. Department <strong>of</strong> Botany, University <strong>of</strong><br />

FloZdGainesvil le, FL 32611.<br />

Light and Electron Microscopy <strong>of</strong> Endogone<br />

pisiformis.<br />

Sporocarpic tissues, including zygosporangia and<br />

zygospores, <strong>of</strong> Endogone pisiformis were examined<br />

with both light and electron microscopy. The<br />

sporocarps are covered by a peridium <strong>of</strong><br />

thick-walled, branched, tapering hyphae that stain<br />

reddish-brown in Melzer's reagent. The<br />

zygosporangia develop from the fusion <strong>of</strong> paired,<br />

apposed gametangia. A primary zygosporangium is<br />

disrupted by an expanding secondary<br />

zygosporangium, within which the zygospore<br />

develops. Zygosporangial and zygospore walls<br />

contrast in staining properties with both light<br />

and electron microscopy. Gametangial septa are<br />

mult iperforate and glebal hyphae possess<br />

infrequent septa with single, central<br />

perforations. The primary constituents <strong>of</strong> the<br />

zygospore cytoplasm are two types <strong>of</strong> lipid globule<br />

that differ in their staining properties.<br />

-- J. L. GIBSON and J. W. Kimbrough. Department <strong>of</strong><br />

Botany, University <strong>of</strong> Florida, Gainesville, FL<br />

32611.<br />

Ultrastructure and development <strong>of</strong> Glaziella<br />

aurantiaca.<br />

Glaziella aurantiaca is a fungus that has been


collected infrequently in lowland tropics and has<br />

been traditional ly placed in the Endogonaceae. The<br />

data here from both light and electron microscopy<br />

indicate that this fungus is an ascomycete. The<br />

septa <strong>of</strong> sporocarpic hyphae have central pores<br />

with plugs <strong>of</strong> electron opaque material and<br />

associated Woronin bodies, a septa1 configuration<br />

typical <strong>of</strong> ascomycetes. The asci form in locules<br />

<strong>of</strong> pseudoparenchyma within the thin walls <strong>of</strong> the<br />

hollow sporocarps. A single, large spore forms<br />

within each ascus. By maturity the ascus wall has<br />

disintegrated and the large ascospore lies within<br />

the remnants <strong>of</strong> the pseudoparenchynatous locule.<br />

Previous researchers have mistaken this unispored<br />

ascus for a terminal chlamydospore and thus<br />

erroneously placed this fungus in the<br />

Endogonaceae.<br />

Gibson, J. L., see Benny, G. L., et. al.<br />

R. L. GILBERTSON. Department <strong>of</strong> Plant Pathology,<br />

University <strong>of</strong> Arizona, Tucson, AZ 85721, and<br />

MEREDITH BLACKWELL. Department <strong>of</strong> Botany,<br />

Louisiana State University, Baton Rouge, LA 70803.<br />

Host and geographical distribution <strong>of</strong> Gulf Coast<br />

wood-rotting fungi.<br />

The Gulf Coast is characterized within the United<br />

States by high average summer and winter<br />

temperatures, long frost free periods, high<br />

rainfall and humidity, and a diverse flora <strong>of</strong> both<br />

hardwood and conifers which act as substrates for<br />

wood-rotting fungi. Temperate, tropical, and<br />

presumed endemic species are characteristic <strong>of</strong> the<br />

fungal flora. We have been particularly interested<br />

in fungi which are associated with living trees.<br />

Some polypore and agaric species associated with<br />

Quercus virginiana (live oak) show a distinct<br />

seasonality <strong>of</strong> fruiting while others are perennial.<br />

Two species are restricted to live oak and several<br />

are more commonly associated with this species than<br />

others in the western gulf region. Species<br />

composition <strong>of</strong> fungi associated with live oak<br />

changes significantly in the western part <strong>of</strong> the 2.<br />

virginiana range. Twenty-five species <strong>of</strong><br />

polypores, agarics, and corticoid fungi are known<br />

to be associated with Juniperus virginiana (eastern<br />

red cedar) in the gulf coast region. Fungal<br />

species composition and frequency are reduced on<br />

this host in central Texas. Only one species<br />

associated with J. virginiana is known to occur on<br />

species <strong>of</strong> western juniper.<br />

Ginns, J. H., see Redhead, S. A.<br />

Glawe, 0. A., see Carris, L. M., et. al.<br />

D. A. GLAWE, and J. D. ROGERS. Dept. <strong>of</strong> Plant Pathology,<br />

Univ. <strong>of</strong> Illinois, Urbana, IL 61801, and Dept.<br />

<strong>of</strong> Plant Pathology, Washington State Univ., Pullman,<br />

WA 99164. Conidial states <strong>of</strong> some species <strong>of</strong><br />

Diatrypaceae and Xylariaceae.<br />

Anamorphs <strong>of</strong> Eutypa spinosa (Pers.: Fr.) Tul. and<br />

Hypoxylon microplacum (Berk. & Curt.) J. H. Yiller<br />

were studied in culture on uotato dextrose anar - (PDA) .<br />

and in moist chambers. Diatrype vicinula (Nyl.) Berl.<br />

Eutypella angulosa (Nits.) Sacc., and Graphostroma<br />

latystoma (Schw.) Pirozynski were cultured on Bonar's<br />

Prodification <strong>of</strong> Leonian's medium, or on PDA amended<br />

with yeast extract. Eutypa spinosa produced a<br />

Selenosporella-like state with sympodially proliferating<br />

conidiogenou~ cells and cylindrical conidia; 11.<br />

microplacum produced a hyphomycetous state with sympodially<br />

and percurrently proliferating conidiogenous<br />

cells and cylindrical conidia; 2. vicinula produced<br />

s<strong>of</strong>t-walled pycnidia, percurrently proliferating conidiogenous<br />

cells, and filiform conidia; g. angulosa<br />

produced irregular, pycnidium-like conidiomata, percurrently<br />

proliferating conidiogenous cells, and cylindrical<br />

conidia; G. platystoma produced a<br />

Nodulisporium state with sympodially proliferating conidiogenous<br />

cells and obovoid to ellipsoid conidia.<br />

Similarities in conidial ontogeny and morphology, as<br />

well as certain resemblances <strong>of</strong> teleomorphs, suggest<br />

that the Diatrypaceae and Xylariaceae are relatively<br />

closely related.<br />

Gochenaur, S. E., see last page <strong>of</strong> abstracts.<br />

ROGER D. GOOS, University <strong>of</strong> Rhode Island, Botany<br />

Department, Kingston, RI 02881. A preliminary<br />

survey <strong>of</strong> aero-aquatic fungi in Rhode Island.<br />

The aero-aquatic fungi are a unique ecological<br />

group, adapted to life in aquatic habitats, where<br />

they develop on submerged vegetation and sporulate<br />

when the substrate becomes exposed to air. Largely<br />

through the work <strong>of</strong> Webster and his associates,<br />

knowledge about the group has expanded markedly in<br />

recent years. Relatively little work has been done<br />

on the group in North <strong>America</strong>. Results <strong>of</strong> surveys<br />

in Rhode Island indicate that the aeroaquatic fungi<br />

are well represented in our area, and have revealed<br />

some new records for North <strong>America</strong>.<br />

Gordon, W. R., see Howell-Major, M.. et. al.<br />

Grassucci, R. A., see Hammill, T. M., et. a1<br />

D. J. GRAY and H. V. AMERSON. University <strong>of</strong><br />

Florida, ItAS AREC, P.O. Box 388, Leesburg, FL<br />

32749-0388 and Botany Department, North Carolina<br />

State University, Raleigh, NC 27650. Potential <strong>of</strong><br />

- in vitro screening for fusiform rust resistance in<br />

l o b m pine embryos.<br />

Fusiform rust (Cronartium uercuum (Berk.) Miyabe<br />

ex Shirai f. sp. fusiformebion <strong>of</strong> loblolly<br />

pine (Pinus taeda -red<br />

in vitro in the same<br />

manner as inivivo. A number<strong>of</strong> tential host<br />

responses to infection were identified fi vitro as<br />

early as 36 hours after basidiospore inomion<br />

including rapid necrosis, cell wall appositions,<br />

periderm and hypertrophy with hyperplasia. The<br />

development <strong>of</strong> rapid necrosis was satistically<br />

correlated with a seed line exhibiting long term<br />

field resistance. This suggested that in vitro<br />

resistance screening could dramatically reTuce the<br />

evaluation time needed to select resistant trees<br />

and seed lines. In addition, incorporation <strong>of</strong> fi<br />

vitro screening with tissue culture propagation may<br />

b e e d to produce elite genotypes not obtainable<br />

with conventional breeding practices.<br />

Gray, L. E., see Carris, L. M., et. al.<br />

C.A. HAMMER AND J.C. CAVENDER. Botany Department. Ohio<br />

University, Athens, Ohio 15701. Dictyostelids in S.E.<br />

Ohio agricultural soils.<br />

A survey <strong>of</strong> dictyostelids in agricultural and forest<br />

soils <strong>of</strong> some S.E. Ohio farms and a seasonal study in<br />

soils <strong>of</strong> four agricultural fields indicate that the<br />

ecolopy <strong>of</strong> sone species is directly affected by agricultural<br />

treatment. In both survey (1 25 soil samples)


26<br />

and seasonal study (450 soil samples), Dictvostelium<br />

sohaerocephalum showed a positive response to pasturing<br />

when adjacent woods or old field are used for comparis011.<br />

A similar but less pronounced response was<br />

noted for 2. mucoroides. Polysphondilium violaceum had<br />

an opposite response. Polysphondilium pallidurn was<br />

found more frequently in the survey from pastures and<br />

old fields than from tilled fields, hay fields or<br />

woods. Both Dictvostelium discoideun and 2. polyceph-<br />

- alum were restricted to the undisturbed forest sites,<br />

while D. aureo-stipes and D. puroureum showed little<br />

or no response to agricultural treatment. Forest soil<br />

had the greatest diversity <strong>of</strong> dictyostelid species,<br />

followed by old fields, pastures, tilled fields and<br />

hay fields. The seasonal study indicated that fluctuations<br />

in total dictyostelid density closely follow<br />

fluctuations in the soil moisture through time and<br />

were most pronounced in soils <strong>of</strong> the woods and old<br />

field. The results demonstrate a possible role for the<br />

cellular slime molds as indicators <strong>of</strong> soil conditions<br />

which may be relevant for enhancing soil biological<br />

input into agricultural systems.<br />

T. M. HAMMILL, S. W. BEATTIE, and R. A. GRASSUCCI.<br />

SUNY-Oswego Laboratory for Ultrastructural Studies,<br />

SUNY College <strong>of</strong> Arts and Science, Oswego, NY 13126.<br />

Scanning electron microscopy <strong>of</strong> zyqosporogenesis in<br />

Mucor mucedo .<br />

--<br />

Mated cultures <strong>of</strong> Mucor mucedo L. :Fr., NRRL 3634 (-)<br />

X NRRL 3635 (+), w - r m 10 C with a photoperiod<br />

<strong>of</strong> 12 h light alternatinq with 12 h darkness.<br />

Primary fixation for SEF! was done for 3 h in an unbuffered<br />

mixture <strong>of</strong> 2% ql utaraldehyde and 2% formal dehyde.<br />

Postfixation was in unbuffered 1% 0s04. Dehydration<br />

in ethanol was followed by transition to<br />

acetone and critical point drying in a Sorvall CPD<br />

System.<br />

The position <strong>of</strong> gametangial septa, formed after fusion<br />

<strong>of</strong> progametangial tips, was determined easily in<br />

SEM images. Suspensors, delimited as a result <strong>of</strong><br />

gametangial septation, contained unequal amounts <strong>of</strong><br />

protoplasmic contents, sugqesting that gametangia<br />

contribute disproportionately to zygospores. Branched<br />

micronyphae were observed commonly over the surface<br />

<strong>of</strong> developing zygospores. The outer wall <strong>of</strong> gametangia<br />

became ruptured and torn as the warty projections,<br />

characteristic <strong>of</strong> mature zygospores, developed from<br />

the underside, initially at the position <strong>of</strong> the fusion<br />

septum. Enlargement <strong>of</strong> zygospore initials was<br />

radial in the plane <strong>of</strong> the fusion septum. Then,<br />

zygospores enlarged toward gametangial septa. As a<br />

result , developing zygospores changed shape from<br />

oblong-ell iptical to spherical. Warty projections on<br />

zyqospores were conical with lonqi tudinal ridges.<br />

They commonly had remnants <strong>of</strong> ruptured wall material<br />

on their tips.<br />

T. M. HAMMILL, S. W. BEATTIE, R. A. GRASSUCCI, D. A.<br />

USSMAN, and C. T. WARE. SUNY-Oswego Laboratory for<br />

Ultrastructural Studies. SUNY Colleae <strong>of</strong> Arts and Science,<br />

Oswego, NY 13126. - ~ransmission electron microscopy<br />

<strong>of</strong> zygosporogenesis in Mucor mucedo. I. Early<br />

stages.<br />

Mated cultures <strong>of</strong> M. mucedo were grown as described<br />

above. Fixation fTr m s according to procedures<br />

published elsewhere by the senior author. Gametangia1<br />

septa, which divided programetangia into gametangia<br />

and suspensors, contained numerous plasmodesmata connecting<br />

suspensors and gametangia. Gametangial septa<br />

developed an electron-opaque layer on the suspensor<br />

side. They also showed a variety <strong>of</strong> swellings. At<br />

the margins <strong>of</strong> gametangial septa, conspicuously thick-<br />

ened areas were formed, suggestive <strong>of</strong> a support function.<br />

The conical "warts," which ornament mature zygospores,<br />

were electron-opaque. They initiated as e-<br />

lectron-opaque thickenings in the developing zygospore<br />

wall,. "Mart" initials appeared on fusion septa, and<br />

it appears that fusion septa may only partially dissolve<br />

and then evaginate rather than dissolve completely.<br />

More work should clarify this. Zygospore<br />

wal! layers are deposited beneath qametangial wall<br />

layers which rupture as a zygospore inflates. "Wart"<br />

initials become confluent at their bases. Protoplasmic<br />

projections into regions between developing<br />

"warts" contained numerous vesicles, consistent with<br />

developmental models for wall deposition. Karyogamy<br />

appears to occur shortly after plasmogamy. Nuclei in<br />

prozygospores <strong>of</strong>ten were seen to have variable shapes<br />

and to contain microtubules. Zygospores developed<br />

numerous lipid qlobules. There is no evidence to date<br />

which supports a zygospore/zygosporangium dichotomy.<br />

Hammons, T. H., see Ellzey, (1. T., et. al.<br />

Harding, K., ,ee Pommerville, J., et. al.<br />

S. D. HARRIS and D. A. COTTER, Department <strong>of</strong> Biology,<br />

University <strong>of</strong> Windsor, Windsor, Ontario, Canada<br />

N9B 3P4. Characterization <strong>of</strong> Saccharmyces<br />

cerevisiae mutants unable to grow in trehalose<br />

containing media.<br />

Haploid vegetative cells <strong>of</strong> the yeast Saccharomyces<br />

cerevisiae contain two trehalase activities. The<br />

activity located in the cytoplasm has a neutral pH<br />

optimum and is responsible for the breakdown <strong>of</strong><br />

endogenously synthesized trehalose. The activity<br />

located in the vacuole is active at an acidic pH<br />

value and has not been assigned a cellular function.<br />

We have found that growth <strong>of</strong> vegetative cells on<br />

exogenous trehalose induces the trehalase activity<br />

which functions at the acidic pH value. Cells grown<br />

on maltose, as well as stationary phase glucose<br />

grown cells also express this activity. We have<br />

isolated a mutant that does not grow on trehalose<br />

or maltose, and fails to express this enzyme activity.<br />

The mutant grows well on glucose and sucrose,<br />

but enters the stationary phase earlier than wildtype<br />

cells. Preliminary evidence indicates that the<br />

mutant is not impaired in trehalose transport.<br />

Arrested mutant cells appear to accumulate carbohydrate<br />

material in the vacuole. These results<br />

suggest that this vacuolar trehalase activity has a<br />

degradative function in glucose depleted cells,<br />

while being specifically induced by growth on<br />

trehalose or maltose.<br />

Harrison, J. A,, see Jaworski, A. J.<br />

Haskins, E. F., see McGuinness, M. D.<br />

E. F. HASKINS and M. D. McGUINNESS. Department o f<br />

Botany, University <strong>of</strong> Washington, Seattle, WA 98195.<br />

Light and electron microscopical studies on Semimorula<br />

liquescens.<br />

Semimorula 1 iquescens is a protoplasmodial slime mold<br />

which produces sessile fruiting bodies. We have<br />

recently discovered the occurrence <strong>of</strong> synaptonemal<br />

complexes during sporulation in this species. The<br />

possible taxonomic affinity <strong>of</strong> this organism with the<br />

Myxomycetes and Protostelia will be discussed.<br />

Heath, M. C., see Meyer, S. L. F.


W. M. HESS. Department <strong>of</strong> Botany and Range<br />

Science, Brigham Young University, Provo, UT<br />

84602.<br />

Invaginations in plasmalemmas <strong>of</strong> grass smut<br />

teliospores (Ustilaqo bullata) viewed by<br />

stereo projection.<br />

Invaginations in plasmalemmas <strong>of</strong> U, bullata<br />

teliospores were studied by freeze-fracture<br />

procedures. More variation was evident in PF<br />

and EF surfaces when spores were wet for 13<br />

hr than when spores were only wet for 6 min<br />

before freezing for f reeze-f racture. Plasma<br />

membranes <strong>of</strong> germinated spores which were not<br />

fixed prior to freezing had fewer disruptions<br />

than plasma membranes <strong>of</strong> spores which were<br />

germinated and fixed. If spores were<br />

germinated then desiccated before freezing<br />

for freeze-fracture, membrane disruptions<br />

were less severe than when spores were<br />

germinated then fixed before freezefracturing.<br />

The only treatment which made it<br />

possible to get consistent images <strong>of</strong> both PF<br />

and EF plasma membrane surfaces was<br />

desiccation followed by wetting spores only 6<br />

min before freezing for freeze-fracturing.<br />

Hinton, D. M., see Racon, C. W.<br />

WILLIAM E. HINTZ, JAMES B. ANDERSON, PAUL A. HORGEN<br />

Dept. Botany, Univ. Toronto, Erindale Campus,<br />

Mississauga, Ont. L5L 1C6. Mitochondria1<br />

inheritance in Agaricus bitorquis.<br />

We have used polymorphisms in mitochondrial (mt) DNA<br />

restriction patterns as phy:ical markers to examine<br />

organelle inheritance in crosses between sexually<br />

compatible strains <strong>of</strong> Agaricus bitorquis. When two<br />

sexually compatible monkaryotic strains are paired,<br />

a fluffy zone <strong>of</strong> mycelium appears at the confluence<br />

<strong>of</strong> the two cultures. The cells in the fluffy zone<br />

are predominately dikaryotic. Usually the zone <strong>of</strong><br />

dikaryotic hyphae remains at the line where the<br />

cultures meet; nuclear migration generally does not<br />

occur in Agaricus. However, a variant strain (Ag<br />

8-11 donates nuclei that migrate in the mycelium <strong>of</strong><br />

some compatible mates following hyphal anastomosis.<br />

In a series <strong>of</strong> crosses between Ag 8-1 and compatible<br />

mates the mitochondrial types <strong>of</strong> the compatible<br />

mates predominated in the dikaryon formed after<br />

nuclear migration from Ag 8-1 had occurred. A<br />

dikaryon (Ag 471, resulting from crossing the<br />

variant Ag 8-1 with a recipient strain Ag 34-2,<br />

carries the same mtDNA and mitochondrial plasmids as<br />

strain Ag 34-2 as determined by mtDNA restriction<br />

analysis, however the copy number <strong>of</strong> the three Ag<br />

34-2 mitochondrial plasmids is greatly increased in<br />

the dikaryon (Ag 47). This suggests that in strains<br />

isogenic for mtDNAs plasmid copy number is<br />

influenced either by the nuclear genotype or by the<br />

nuclear status (monokaryotic vs dikaryotic) <strong>of</strong> the<br />

strain.<br />

H. H. HO. Department <strong>of</strong> Biology, State University<br />

<strong>of</strong> New York, NY 12561. The validity <strong>of</strong> Phytophthora<br />

melonis and P. sinensis. --<br />

Phytophthora melonis was erected by Katsura (1968)<br />

as the causal agent <strong>of</strong> foot rot <strong>of</strong> cucumber in<br />

Japan. It was characterized by semi-papillate,<br />

non-proliferating sporangia and chlamydospores.<br />

Since then, a similar disease known as dieback,<br />

root rot, crown rot or blight was reported on<br />

various cucurbits in Egypt, Iran, Taiwan and the<br />

2 7<br />

mainland <strong>of</strong> China, but the pathogen was identified<br />

as p. drechsleri, p. melonis or p. sinensis sp. nov.<br />

9 comparative study <strong>of</strong> these isolates with the type<br />

or authentic cultures <strong>of</strong> p. drechsleri, g. melonis<br />

and p. sinensis was conducted and they were found<br />

to be similar in cultural, morphological and pathological<br />

characteristics. The original description<br />

<strong>of</strong> p. melonis was inaccurate and misleading, because<br />

upon re-examination, the type culture produced<br />

distinctly non-papillate and internally proliferating<br />

sporangia in water and chlamydospores could not<br />

be found. Since P. sinensis was erected solely<br />

based on comparison with Katsura's erroneous description,<br />

the new epithet is not warranted. When<br />

studied under similar cultural conditions, neither<br />

-- P. melonis nor p. sinensis was specifically distinct<br />

from p. ,drechsleri. Thus, to avoid further nomenclatural<br />

confusion, both p. melonis and p. sinensis<br />

should be treated as synonyms <strong>of</strong> p. drechsleri which<br />

has priority.<br />

Hocking, A. D., see Pitt, J. I., et. al.<br />

Horgen, P. A., see Hintz, W. E., et. al.<br />

Horgen, P. A., see Horton, J. S.<br />

Horgen, P. A., see rleyer, R. J., et. al.<br />

P.A. HORGEN. Mushroom Research Group, Univ. <strong>of</strong><br />

Toronto, Erindale Campus, Mississauga, Ont. L5L 1C6<br />

Biotechnological Approaches to Mushroom Strain<br />

Improvement, Are They Possible?<br />

Three unique plasmid-like DNA components were isolated<br />

from a strain <strong>of</strong> Agaricus bitorquis. The DNA<br />

moieties were linear, possessing regions <strong>of</strong> terminal<br />

inverted repeated sequences. Plasmid-like DNAs have<br />

been observed in a number <strong>of</strong> wild Agaricus isolates;<br />

no plasmid-like DNAs have been found in cultivated<br />

strains <strong>of</strong> A. bisporus. No homology was detected between<br />

the plasmids and the nuclear or mitochondrial<br />

genomes <strong>of</strong> either wild or cultivated Agaricus. The<br />

three plasmids are distinctly different and appear to<br />

independently replicate. Restriction fragments <strong>of</strong><br />

the mushroom plasmids have been cloned. Inorgennello<br />

transcription and translation <strong>of</strong> Agaricus mitochondria<br />

will determine if the plasmid DNA sequences<br />

carry any expressed genetic information. Transformation<br />

strategies using antibiotic resistance genes and<br />

mushroom plasmid origins <strong>of</strong> replication will be discussed.<br />

Heterologous hybridization approaches have<br />

been used to isolate specific gene sequences for both<br />

nuclear and mitochondr ial genes for Agaricus. These<br />

sequences will provide a preliminary gene bank for<br />

Agaricus. Mitochondria1 DNA studies indicate that<br />

considerable restriction pattern heterogeneity exists<br />

in the wild Agaricus while none exists in the cultivated<br />

Agaricus. The genome size <strong>of</strong> A. bitorquis is<br />

twice that <strong>of</strong> A. bisporus. Preliminary evidence suggests<br />

that mitochondrial genome type and mushroom<br />

plasmid copy number may be under nuclear control.<br />

The feasibility <strong>of</strong> using recombinant DNA approaches<br />

to genetically alter the commercial mushroom will be<br />

discussed.<br />

J.S. HORTON and P.A. HORGEN. Department <strong>of</strong> Botany,<br />

Erindale Campus, Univ. <strong>of</strong> Toronto, Mississauga, Ont.<br />

L5L 1C6. The steroidal regulation <strong>of</strong> gene products<br />

in Achlya.<br />

The addition <strong>of</strong> antheridiol to undifferentiated cultures<br />

<strong>of</strong> Achlya elicits several changes in macromolecular<br />

syntheses during the ontogeny <strong>of</strong> antheridiol<br />

branch initials. There is an enhancement <strong>of</strong>


28<br />

RNA and protein synthesis suggesting both gene<br />

activation and gene product accumulation. Both<br />

ribosomal and poly (A+) mRNA are stimulated by<br />

antheridiol. The pheromone affects the acetylation<br />

<strong>of</strong> histones prior to mRNA synthesis and branch<br />

initiation. In vitro measurements indicate that<br />

antheridiol and a cytosol component (receptor).<br />

dramatically stimulate transcription. We have also<br />

measured the levels <strong>of</strong> RNA polymerase I1 during male<br />

development utilizing immunological techniques.<br />

Changes <strong>of</strong> protein populations during female<br />

development have been examined. Most recently, an<br />

antheridiol-induced basic polypeptide <strong>of</strong> 64,000<br />

daltons (ABP) has been identified. The qualitative<br />

synthesis <strong>of</strong> ABP commenced 30-60 minutes after<br />

antheridiol addition and continued for 6 hours. ABP<br />

synthesis in male E87 was detected throughout sexual<br />

morphogenesis in matings with the female 734. Two<br />

other species <strong>of</strong> Achlya also synthesized ABP in<br />

response to antheridiol. Synthesis <strong>of</strong> the inducible<br />

polypeptide was not associated with a general<br />

branching response. Studies using actinomycin D<br />

suggested a transcriptional control <strong>of</strong> ABP. We are<br />

presently constructing a cDNA library and will be<br />

screening this library for ABP sequences using<br />

differential colony hybridization.<br />

2. R. HOSFORD. Dept. <strong>of</strong> Biolopical Sciences, Central<br />

Llashington University, El lensburn, \.!A SG926.<br />

Mutinus xylogenus: a rare phalloid found in the<br />

Amazon Basin.<br />

A rare phalloid collected in the Amazon Basin, is<br />

identified as Mutinus xylogenus. This, the third<br />

known report <strong>of</strong> the species since 1855, extends the<br />

range to Brazil and confirms a very narrow equatorial<br />

distribution. The species is distinquished by its<br />

1) minute size (up to 5 mn tall), 2) epixylous habit,<br />

and 3) glebal mass covering the apex <strong>of</strong> the receptacle.<br />

A1 though some workers have placed the species<br />

in the monotypic genus Xylophallus, the author<br />

retains it in the genus Mutinus.<br />

R. J. HOWARD. E. I. duPont de Nemours & Co., Inc.<br />

Agricultural Chemicals Department, Experimental<br />

Station, Wilmington, DE 19898.<br />

Freeze-substitution.<br />

Freeze-substitution is a fixation and dehydration<br />

technique for the preparation <strong>of</strong> specimens for microscopy.<br />

Fixation is initially accomplished by<br />

rapid freezing. Frozen samples are dehydrated,<br />

chemically fixed with OsO at low temperatures,<br />

embedded and thi n-secti odd. The technique <strong>of</strong>fers<br />

the enormous advantages <strong>of</strong> cry<strong>of</strong>ixation in samples<br />

that are examined in section: better preservation <strong>of</strong><br />

cellular structure (cf. J. Ultrastruct. Res. 66:224,<br />

J. Cell Sci. 48:89, Protoplasma 103:281, Exp. Mycol.<br />

5: 167) and new opportunities for imnunocytochemistry.<br />

Freeze-substitution is ideally suited for the preparation<br />

<strong>of</strong> cells grown in monolayers or suspension<br />

but also can be used for the study <strong>of</strong> some tissues.<br />

Each step in the freeze-substitution process will be<br />

considered so that the interested investigator is<br />

prepared for the afternoon demonstration.<br />

YP:IGAXT i-IQ-PNOR, W. a. CX)RDON, and L. FEDERICK.<br />

Howard University, Washington, DC 20059 Protein and<br />

esterase patterns <strong>of</strong> isolates <strong>of</strong> a natural mutant <strong>of</strong><br />

. Pleuro~ra<br />

--- -- . dodqei -----, a wi ld t w strain, and FJ. te~~i--<br />

c9&-<br />

Protein 3nd esterasn p.tterns <strong>of</strong> mycelial extdacts <strong>of</strong><br />

four isolates <strong>of</strong> a spontaneous mutant <strong>of</strong> Neurospora<br />

. dcdaei s homthallic species, have been compared<br />

L-.<br />

with those <strong>of</strong> isolates <strong>of</strong> t!e wild type and <strong>of</strong> M.<br />

-- terricola. Morpholcqically, the mutant is distinwished<br />

from the wild type and from 3. terricola by<br />

its round or peanut px?-sha@ ascos-mres t!at m~y<br />

vary in n3unber from 8 to 16 psr ascus. Pr<strong>of</strong>iles were<br />

separated on vertical polyacrylamide gel electrophoresis.<br />

Clear differences have heen found between<br />

protein pr<strong>of</strong>iles <strong>of</strong> the wild type, the mutant isolates,<br />

and N. terricola. Twenty-tm protein bands<br />

appear to distinguish the wild type <strong>of</strong> the species.<br />

Isolates <strong>of</strong> the mutant have yielded patterns with<br />

up to 30 separate banes. Sixteen bands have been<br />

comn to all isolates studied. In the protein<br />

pr<strong>of</strong>iles <strong>of</strong> the different isolates bands were<br />

present that were unique to each strain. Distinct<br />

differences hav? also ken noted in esterase<br />

patterns <strong>of</strong> the strains studied.<br />

F.-S. HU and J. CLARK School <strong>of</strong> Biological Sciences,<br />

University <strong>of</strong> Kentucky, Lexington, Kentucky 40506.<br />

Mitochondria <strong>of</strong> senescing Physarum polycephalum<br />

plasmodia.<br />

Plasmodia <strong>of</strong> the myxomycete Physarum polycephalum<br />

undergo senescence after a period <strong>of</strong> growth as macroplasmodia<br />

on agar medium, but appear to be immortal<br />

when grown as microplasmodia in shake culture. These<br />

and other culture studies were the basis for a<br />

hypothesis that senescence is due to the infectious<br />

degeneration <strong>of</strong> an organelle (mitochondrion) similar<br />

to that reported in Podospora anserina mycelia.<br />

Therefore, the mitochondria <strong>of</strong> young, senesci ng and<br />

immortal plasmodia have been examined for differences<br />

in morphological structure and DNA content. For<br />

senescing plasmodia there appears to be an increase<br />

in the number and size <strong>of</strong> spherical osmophilic bodies<br />

that are present in the mitochondria, but to date no<br />

indication <strong>of</strong> mi tochondri a1 DNA changes have been<br />

found.<br />

F.-S. HU, S. STEINER and J. CLARK School <strong>of</strong> Biological<br />

Sciences, University <strong>of</strong> Kentucky, Lexington,<br />

Kentucky 40506.<br />

Phospholipids <strong>of</strong> Physarum polycephalum and Didymium<br />

iridis.<br />

Axenic semi-defined shake cultures <strong>of</strong> Phjsarum polycephalum<br />

plasmodia and heat-killed bacteria supplemented<br />

corn-meal agar cultures <strong>of</strong> Didymium iridis<br />

plasmodia and myxamoeba were labeled with radioactive<br />

phosphate and the phospholipids extracted with a<br />

chlor<strong>of</strong>orm-methanol system. The individual phospholipids<br />

were then isolated by 2-dimensional chromatography<br />

on partially EDTA-impregnated silicic acid<br />

paper, located by autoradiography and quantitated by<br />

scintillation spectroscopy. The phospholipid composi<br />

tion <strong>of</strong> Didymium i ridi s plasmodia is 38% phosphatidylethanolamine,<br />

35% phosphatidylchol ine, 12%<br />

phosphatidyli nosi to1 , 5$ phosphatidylserine, 4%<br />

~hos~hatidvlalvcerol<br />

- -- . 2.5% cardioli~id. 0.5% ~hosohatidic<br />

acid and 4% unidentified lipids. -~he phospholipids<br />

<strong>of</strong> Didymium iridis myxamoeba and ~hysarum<br />

polycephalum plasmodia are,similar. A fraction <strong>of</strong> the<br />

unidentified lipids are a1 kaline-stable s~hinaoli~ids.<br />

some <strong>of</strong> which were sugar-contai ni ng and had t6e chro--<br />

matographi c properties <strong>of</strong> sphi ngoglycol i pi ds. The<br />

a1 kal ine-stable lipid composition <strong>of</strong> the P. polycep-<br />

&plasmodium and Q. iridis myxamoeba were similar<br />

in that they each contained four chromatographically<br />

similar sphingolipids, while the D. iridis plasmodium,<br />

on the other hand, displayed only a single major<br />

alkaline-stable lipid.


Hubbes, Y., see Spielman, L. J.<br />

R. A. HUMBER. USDA Insect Pathology Research Unit,<br />

Boyce Thompson Institute, Tower Rd., Ithaca, NY 14853.<br />

PhpZogenetic position <strong>of</strong> the EntomophthoraZes within<br />

the Zggomycetes.<br />

Several diverse lines <strong>of</strong> evidence indicate that the<br />

Entomophthorales occupy a primitive position anmg<br />

all zygomycete orders. Asexual propagules in the<br />

EntomophthoraLes arise as conidia and cannot be<br />

regarded as sporangioles; further,,these conidia<br />

develop so rapidly after discharge that they <strong>of</strong>ten<br />

behave more like thallic propagules than differentiated<br />

spores. It appears that the common mucoroid<br />

sporangium did not evolve until after the Entomophthorales<br />

had diverged from the ancestral zygomycete<br />

line. Zygosporogenesis in the Entomophthorales is<br />

strictly homothallic.and morphologically simple. The<br />

heterothallic mating systems <strong>of</strong> mucoroid fungi and<br />

hormonally mediated development, unusual behavioral<br />

patterns <strong>of</strong> approaching gametangia in many genera,<br />

and decorations <strong>of</strong> the zygophores in genera such as<br />

Phycomyces indicate that these mucoroid fungi are<br />

more evolutionarily advanced than entomophthoralean<br />

fungi. Nuclei <strong>of</strong> mucoroid fungi and the Ancylistaceae<br />

(the most primitive <strong>of</strong> the three entomophthoralean<br />

families) are similar in size and appearance.<br />

However, the spindle polar structures <strong>of</strong> mucoroid<br />

fungi have been found to be intranuclear while those<br />

<strong>of</strong> the Entomophthorales and all other fungi investigated<br />

so far are extranuclear.<br />

T. ITURRIAGA and C. BREWER. Jardin Botanico de<br />

Caracas, Apartado. 2156, Caracas, Venezuela and<br />

Apartado 1998, Caracas 1010A, Venezuela.<br />

Cerro Neblina Expeditions.<br />

Cerro Neblina is a National Park, with an area <strong>of</strong><br />

1,360,000 hectares, located in the southernmost part<br />

<strong>of</strong> Venezuela along its border with Brazil. It is<br />

located at 0'40" north <strong>of</strong> the equator, and its altitude<br />

is 3.014 meters above sea level. It is the<br />

highest elevation in the Guayana <strong>of</strong> Venezuela.<br />

Its interest relies in the fact that it is an unexplored<br />

region, and it is one <strong>of</strong> the most isolated and<br />

least known <strong>of</strong> the mountains <strong>of</strong> the Guayana Highland.<br />

The Highland area belongs to the Guayana shield, one<br />

<strong>of</strong> the oldest parts <strong>of</strong> South <strong>America</strong>. Flora and Fauna<br />

are very poorly known. In Cerro Neblina altitudes<br />

extend from 100 meters in the lowland rainforest to<br />

3040 meters on the peaks, in a linear distance <strong>of</strong> 6<br />

km. It is considered as one <strong>of</strong> the most diverse<br />

tepuy-systems in the Guayana because <strong>of</strong> its biological<br />

diversity. Expeditions have continued for one year,<br />

and up to now 120 scientists have participated.<br />

Zoological and botanical collections amounting to<br />

20,000 specimens from 12 camps. Many new species,<br />

some new genera, one new family, and numerous<br />

endemic species to that region have been found.<br />

A. J. JAWORSKI and J. A. HARRISON, Botany Department<br />

University <strong>of</strong> Georgia, Athens, Georgia 30602<br />

Two regulatory classes <strong>of</strong> messenger RNA in<br />

Blastocladiella emersonii zoospores.<br />

Previous work had shown that B. emersonii zoospores<br />

contained messenger RNA that was synthesized<br />

during the growth phase (GPrnRNA) and late sporulation<br />

(LSmRNA). GPmRNA in the zoospore is bound to 80s<br />

monoribosomes while the LSmRNA is bound to polyribo-<br />

29<br />

somes. Studies using the wheat germ in vitro protein<br />

synthesizing system and aurintricarboxylic acid (an<br />

inhibitor <strong>of</strong> protein synthesis initiation) confirmed<br />

that both GPmRNA and LSmRNA have completed the<br />

initiation steps <strong>of</strong> protein synthesis and are blocked<br />

from translstion at some stage <strong>of</strong> elongation.<br />

During the first sixty minutes <strong>of</strong> sporulation,<br />

polyribosomes disaggregate into 80s monoribosomes.<br />

During later stages <strong>of</strong> sporulation these ribosomes<br />

re-assemble into polyribosomes. At Tt8 (60 minutes<br />

into sporulation) GPmRNA is found on S ribosomes.<br />

A portion <strong>of</strong> the GPmRNA re-assembles into polyribosomes<br />

by T180, but from T until zoospore release,<br />

polyribosomes containing E@%NA disassemble. During<br />

this transition. LSmRNA is synthesized and is found<br />

exclusively on zoospore polyribosomes.<br />

Analysis <strong>of</strong> in vitro activity <strong>of</strong> zoospore<br />

monoribosomes and polyribosomes in the wheat germ<br />

S150 system revealed that only zoospore pol.yribosomes<br />

were active. Likewise, only RNA extracted from zoospore<br />

polyribosomes was active in the wheat germ S30<br />

system. The factor(s) responsible for the translation<br />

inhibition <strong>of</strong> 80s monoribosomes has not been<br />

identified. Supported by NSF Grant PCM 83.09775.<br />

D.T.JENKINS. Biolog! Dept., University <strong>of</strong> Alabama at<br />

Birmingham, Birmingham, AL 35294. The Genus Amanita<br />

in the Southeastern United States.<br />

In the southeastern U.S. members <strong>of</strong> the genus Amanita<br />

compose one <strong>of</strong> the rest conspicuous and beautiful segments<br />

<strong>of</strong> the myc<strong>of</strong>lora. The very ornate fruit bodies<br />

<strong>of</strong> Amanita cokeri, the large size <strong>of</strong> Amanita daucipes<br />

or Amanita polypyrmis, the very bright colors <strong>of</strong><br />

Amanita caesarea or Amanita parcivolvata, the small,<br />

delicate appearance <strong>of</strong> Amanita farinosa, these and<br />

many other examples can be used to illustrate the<br />

uniqueness <strong>of</strong> this F.enus among the southern mushrooms.<br />

Due to the combination <strong>of</strong> environmental and geographic<br />

factors and the variety <strong>of</strong> forest types, the southeastern<br />

U.S. is recc.gnized as one <strong>of</strong> the best localities<br />

in the world for collecting and studying members<br />

<strong>of</strong> this genus. Coll.ecting seasons are usually long<br />

and rainfall more than adequate for their growth.<br />

Since it is suspected that most Amanitas are mycorrhizal,<br />

the great variety <strong>of</strong> forest types allows for the<br />

growth <strong>of</strong> many different taxa. From the mixed deciduous<br />

and pine forests <strong>of</strong> the Appalachian mountains to<br />

the longleaf pine-turkey oak forests <strong>of</strong> the gulf<br />

ccastal regions. meribers <strong>of</strong> this genus are an intricate<br />

part <strong>of</strong> the forests systems. The purpose <strong>of</strong> this<br />

presentation is to provide a panorama <strong>of</strong> the genus<br />

Amanita in the sout!leastern U.S. Representative slides<br />

from some <strong>of</strong> the nearly 100 taxa recognized from this<br />

region will be shown. Unique morphological features<br />

will be highlighted taxonomic relationships will be<br />

clarified, and mycolrrhizal possibilities discussed.<br />

Johnson, J. L., see V il galys, R., et. a1 .<br />

Jones, J. P., see Tuttle, G. A.<br />

HAROLD W. KELLER and JEAN D. SCHOKNECHT. Department <strong>of</strong><br />

Biology, The University <strong>of</strong> Texas at Arlington,<br />

Arlington, TX 76019 and Department <strong>of</strong> Life Sciences,<br />

Indiana State University, Terre Haute, IN 47809.<br />

A new species <strong>of</strong> Didymium (Myxomycetes) isolated from<br />

bovine dung.<br />

Moist chamber cultures <strong>of</strong> bovine dung collected from<br />

the Pawnee National Grassland in Colorado have yielded<br />

abundant sporangia <strong>of</strong> a new species <strong>of</strong> Didymium.<br />

Spore to spore cultivation was completed on sterilized


ovine dung and on agar under controlled laboratory<br />

conditions. The phaneroplasmodium is milky white.<br />

This taxon typically forms white, subglobose sporangia<br />

0.2 to 0.4 mrn in diameter. occasionally producing<br />

straight or branched plasmodiocarps up to 1.5 mm in<br />

length. It belongs to the group <strong>of</strong> Didymia with<br />

crystalline, white, eggshell-like peridia. Some <strong>of</strong><br />

the larger fructifications contain crystalline bodies<br />

attached to capillitial threads. A columella is<br />

absent, and the fruiting bodies contain abundant,<br />

typical didymiaceous capillitium. The spores are<br />

echinulate, 9-10 pm in diameter, and subglobose,<br />

encircled by an equatorial ridge that serves as the<br />

site for spore wall dehiscence at germination. The<br />

spores are reminiscent to those <strong>of</strong> Didymium saturnus<br />

Keller. The sporangia <strong>of</strong> this new taxon resemble<br />

Didymium nullifilum (Kow.) Farr, but differ in the<br />

abundant capillitium and spores with an equatorial<br />

ridge.<br />

R. W. Kerrigan. Department <strong>of</strong> Biological<br />

Sciences, University <strong>of</strong> California, Santa<br />

Barbara, CA 93106. Systematics and<br />

potential utilization <strong>of</strong> the genus Agaricus.<br />

Phenotypic plasticity, apparent polymorphism,<br />

and a lack <strong>of</strong> distinctive micr<strong>of</strong>ea tures complicate<br />

the systematics <strong>of</strong> Agaricus at the<br />

species level. It is less difficult, however,<br />

to recognize infrageneric species<br />

groupings. Biochemical features have become<br />

increasingly important in delimiting sections<br />

<strong>of</strong> Agaricus. The occurrence and properties<br />

<strong>of</strong> mushroom phenoloxidases are particularly<br />

useful in this regard. One section, Horten-<br />

ses, comprises the widely cultivated species<br />

- A. bisporus and its allies. The relationships<br />

in this group appear to be quite close;<br />

analysis on the basis <strong>of</strong> morphology alone is<br />

difficult. Complementary biochemical and/or<br />

molecular approaches would seem well suited<br />

to the resolution <strong>of</strong> such problems.<br />

The phylogeny <strong>of</strong> A. bisporus, and the<br />

relationship <strong>of</strong> wild to cultivated strains,<br />

is at present unclear. There are indications<br />

that wild strains may have greater disease<br />

resistance than do cultivated strains. There<br />

may exist in nature a large and untapped pool<br />

<strong>of</strong> genetic variation useful in crop improvement.<br />

Study <strong>of</strong> the tetrasporic ancestral<br />

complex may indicate how traits such as spore<br />

number are controlled, perhaps leading to<br />

cultivated heterothallic strains. Species<br />

with different initiation requirements could<br />

help to reveal how initiation proceeds.<br />

R. W. Kerrigan and I. K. Ross. Department <strong>of</strong><br />

Biological Sciences, University <strong>of</strong> California,<br />

Santa Barbara, CA 93106. Further<br />

investigations <strong>of</strong> spore number in Agaricus.<br />

Recent experiments and observations lend<br />

further support to the concept <strong>of</strong> basidiospore<br />

number as a dynamic phenomenon.<br />

Earlier hypotheses regarding the influence <strong>of</strong><br />

sporocarp age and harves t-related stress on<br />

spore number may have been incorrect. Low<br />

temperature, on the other hand, has repeatedly<br />

been found to cause a pronounced reduction<br />

in average spore number. There are indications<br />

<strong>of</strong> additional factors possibly influencing<br />

the extent to which three- and twospored<br />

basidia may occur in the hymenium <strong>of</strong><br />

predominately tetrasporic species.<br />

Current knowledge regarding the nuclear<br />

and/or genetic composition <strong>of</strong> spores borne<br />

upon three- and two-spored basidia w i l l be<br />

presented.<br />

J.L.Kerwin,Christopher A.Simmons and R.K.Washino.<br />

Dept. <strong>of</strong> Entomology, University <strong>of</strong> California, Davis,<br />

CA 95616. Regulation <strong>of</strong> oosporogenesis by Lagenidium<br />

giganteum.<br />

Induction and maturation <strong>of</strong> Lagenidium giganteum oospores<br />

are complex developmental processes influenced<br />

by exogenous lipid media supplements and a variety <strong>of</strong><br />

calcium-dependent events. Sterols, which are necessary<br />

for induction <strong>of</strong> oosporogenesis, enhance uptake <strong>of</strong><br />

fatty acids from growth media. Unsaturated 16- and<br />

18-carbon fatty acids increase oospore induction and<br />

maturation. Enrichment <strong>of</strong> the fatty acyl compounds <strong>of</strong><br />

the fungus with unsaturated moieties appears to affect<br />

cyclic nucleotide metabolism and promotes cellular and<br />

vesicular fusion events by regulating membrane fluidity.<br />

Using a variety <strong>of</strong> inhibitory compounds, the<br />

calcium-binding protein calmodulin and calcium-specific<br />

channels have been implicated in L. giganteum oosporogenesis.<br />

Hypotheses concerning the role <strong>of</strong> calcium<br />

in regulating cellular and vesicular fusion are<br />

presented.<br />

ST. W. KIMBROUGH. Department <strong>of</strong> Botany, university<br />

<strong>of</strong> Florida, Gainesville, FL 32611. The twilight<br />

years <strong>of</strong> W. A. Murrill in Florida.<br />

After resigning as Director-in-Chief <strong>of</strong> the New<br />

York Botanical Garden in August, 1924, W. A. Murrill,<br />

after a few years <strong>of</strong> wandering, settled in Florida<br />

where he spent approximately 30 years around the<br />

University <strong>of</strong> Florida in Gainesville. As noted by<br />

Pr<strong>of</strong>. George F. We3er (Mycologia 53: 543-557), Dr.<br />

Murrill left the Garden as a very troubled man.<br />

Health problems continued to plague him and were<br />

perhaps responsible for his remaining in Gainesville.<br />

Through the concern and attention <strong>of</strong> Pr<strong>of</strong>essors<br />

George Weber and Erdman West, Curator <strong>of</strong> the Herbarium,<br />

Dr. Murrill was able to regain his strength<br />

and composure. In was during his first summer months<br />

in Gainesville that Dr. Murrill became enthused by<br />

the large number <strong>of</strong> mushrooms that weremew to him.<br />

His previous trips to Florida had evidently been<br />

for short visits during the winter months.<br />

During my first years in Gainesville, Pr<strong>of</strong>. WeLer<br />

and I were fortunate to have opportunities to visit<br />

with Dr. Fred Seaver in Winter Park, Florida. It<br />

was during these visits that I learned many interesting<br />

things about Murrill and his activities. It is<br />

these and other undocumented events that I would<br />

like to present to you today.<br />

Kimbrough, J. W., see Benny, G. L., et. al.<br />

Kimbrough, J. W., see Gibson, J. L.<br />

Kinney, A. J., see Rlackwell, Y., et. al.<br />

---<br />

M. A. KLICH. U. S. D. A. Southern Regional<br />

Research Center, P.O. Box 19687, New Orleans,<br />

LA 70179. Prediction <strong>of</strong> the susceptibility <strong>of</strong><br />

cotton plants to invasion by Aspergillus<br />

f lavus.<br />

Cotton grown in the low desert areas <strong>of</strong> the USA<br />

is susceptible to invasion by Aspergillus flavus<br />

-.


Link. The 'fungus produces ailatoxin, a potent<br />

carcinogen, in the cotton seed. In order to assess<br />

the feasibility <strong>of</strong> certain control measures,<br />

field studies on the ecology <strong>of</strong> the fungus were<br />

undertaken. Results have shown that the fungus<br />

may enter the plant through a variety <strong>of</strong> natural<br />

openings and move up into the seeds <strong>of</strong> developing<br />

bolls. Receptivity <strong>of</strong> the plant to invasion via<br />

these natural openings does not remain constant<br />

through the growing season. A. flavus inoculated<br />

onto the involucral nectaries <strong>of</strong> flowers caused<br />

significant increases in contamination levels<br />

in seeds from early season flowers, but not from late<br />

season flowers. We found that bolls from early<br />

season flowers remained susceptible to mold invasion<br />

through the involucral nectaries for 25-30 days<br />

after anthesis. Susceptibility <strong>of</strong> early season<br />

flowers is strongly influenced by drought stress.<br />

Plants with noon water potential readings between<br />

1.6 and 1.9 MPa were most susceptible to invasion<br />

by A. flavus. A preliminary predictive model for<br />

fungal invasion <strong>of</strong> cotton plants, based on tine <strong>of</strong><br />

flowering and water potential, has been developed.<br />

L.M. KOHN. Dept. <strong>of</strong> Botany, University <strong>of</strong> Toronto,<br />

Erindale College, Mississauga, Ontario L5L 1C6,<br />

Canada. Microconidial anamorphs: A new source <strong>of</strong><br />

characters in the Helotiales?<br />

Microconidia produced from phialides are<br />

characteristic <strong>of</strong> the Sclerotiniaceae and are<br />

produced by at least one species <strong>of</strong> the<br />

Dermateaceae. Both in the field and under standard<br />

laboratory conditions, microconidia fail to germinate<br />

vegetatively; in a few cases, they have been<br />

demonstrated to function as spermatia. Under the<br />

assumption that they show little morphological or<br />

ontogenetic diversity, previous workers have left a<br />

legacy <strong>of</strong> poor descriptions and illustrations and<br />

have failed to exploit these morphs as a source <strong>of</strong><br />

characters. On the basis <strong>of</strong> preliminary review, some<br />

microconidial anamorphs, eg., those associates with<br />

the genus Botryotinia Whetzel, show little variation,<br />

while others, eg., that associated with Ciborinia<br />

camelliae Kohn, are distinctive for a single<br />

teleomorphic species. The possibility that<br />

microconidial characters have been highly conserved<br />

in some teleomorphic genera yet have diversified in<br />

others may <strong>of</strong>fer insight into inter- and<br />

infra-generic relationships in the Sclerotiniaceae,<br />

as well as into familial relationships in the<br />

Helotiales. Microconidial anamorphs may be analysed<br />

on the following criteria: location <strong>of</strong> anamorph<br />

within the host, presentation <strong>of</strong> phialides, phialidic<br />

and microconidial morphology, microconidiogenesis,<br />

and presence and color <strong>of</strong> mucilage. Existing<br />

accommodation <strong>of</strong> some microconidial anamorphs in<br />

form-genera such as Myrioconium Sydow should be<br />

further refined to codify descriptions.<br />

Koons, K., see Wach, M. P., et. al.<br />

Koske, R. E., see Gemma, J. N.<br />

R. E. KOSKE. Department <strong>of</strong> Botany, Univ. <strong>of</strong> Rhode<br />

Island, Kingston, RI 02881. The VA mycorrhizal<br />

fungal community <strong>of</strong> Seashore State Park, Virginia.<br />

Seventeen species <strong>of</strong> VAM fungi were isolated from the<br />

sand dunes at Seashore State Park, Virginia Beach,<br />

Virginia. Average species richness (no. VAMF species1<br />

root zone) was 5.0 for plants <strong>of</strong> Ammo hila brevil i u<br />

lata (range 2-8) and 8.5 for Unio +!-(-a aniculata range<br />

m). The average species richnessPfor this site<br />

(all host species) was 6.11, extending the observation<br />

31<br />

<strong>of</strong> increasing average species richness along the<br />

Atlantic Coast dunes with decreasing latitude. Importance<br />

values (IV) were calculated for VAMF species by<br />

sumning their relative frequency, relative density,<br />

and relative dominance. The latter parameter is<br />

derived from the product <strong>of</strong> spore density and spore<br />

volume. The maximum possible value for IV is 300.<br />

On the basis <strong>of</strong> their IV. the dominant species <strong>of</strong> VAM<br />

fungi at the site were ~lomus tortuosum (1~=90.0),<br />

Acaulospora scrobiculata.<br />

~ani'er, J. L., see Yates, I. E., et. al.<br />

Lewis, 0. P., see Cibula, W. G., et. al.<br />

A.E. LIBERTA and R.C. ANDERSON. Department <strong>of</strong> Biological<br />

Sciences, Illinois State University, Normal, IL<br />

61761. Comparison <strong>of</strong> VM1 species composition, spore<br />

abundance, and inoculwn potential in an Illinois<br />

prairie and selected agricultural sites.<br />

Three VAbf parameters were compared for five sites at<br />

Weston Cemetery Prairie (Nos. 1-S), for adjacent inorganically<br />

fertilized corn and oat fields (site Nos.<br />

6 & 7), and for an organically fertilized corn field<br />

(site No. 8) located in a nearby Illinois county.<br />

Sites 1-6 were sampled in July, 1982 & 1984, while<br />

sites 7 & 8 were sampled in July, 1984. Spore analysis<br />

showed Gtomub ~ a d to be c the ~ most abun- ~<br />

dant taxon at all sample sites in both 1982 & 1984,<br />

and G. geodpohwn to be present at all sample sites except<br />

No. 8. Other species represented at two or more<br />

<strong>of</strong> the five prairie sites were G. culedoniwn, G. moddeae,<br />

Gigig~poha ~ o d p o and ~ , G. m#cgcvr&. Sites<br />

6 & 7 also contained spores <strong>of</strong> G. mahgahita. Oneway<br />

ANOVA <strong>of</strong> total spores per site showed no significant<br />

differences between sites in 1984, but significant<br />

differences between sites 1,2,4, & 6 in 1982. However,<br />

for the 1984 data, oneway ANOVA'S <strong>of</strong> spore<br />

counts for each species by site revealed significant<br />

(P < 0.05) differences between sites for G. ~u.~c~cu-<br />

.k&m and G. mahgahita. Sites 6,7, & 8 had significantly<br />

lower spore counts for G. 6~cicd.eatum than<br />

the prairie sites, and sites 6 & 7 had significantly<br />

higher counts for G. mc~gatLita than the other sites.<br />

Spores <strong>of</strong> G. mchocahyxun and Sc~c~ocyd.tid ninuoda<br />

were only isolated from site No. 8. Oneway ANOVA<br />

showed that VAbf colonization was significantly lower<br />

for bioassay plants grown in soil from sites 7 & 8<br />

than for those grown in soil from other sites.<br />

Lingle, W. L., see Barstow, W. E., et. al.<br />

W.L. LINGLE* D.J. O'KANE~, D. PORTER*, and<br />

J.E. WAMPLER~. "Department <strong>of</strong> Botany and<br />

t~e~artment <strong>of</strong> Biochemistry, University <strong>of</strong><br />

Georgia, Athens, GA 30602. Localization <strong>of</strong><br />

light emitting tissue in the bioluminescent<br />

mushroom, PaneZZus stipticus.<br />

Fruiting bodies <strong>of</strong> PaneZZus stipticus (Bull.<br />

: Fr.)Kar. emit light steadily for extended<br />

periods with peak emission at 535 nm. The<br />

bioluminescence capacity develops with the.<br />

fruiting body. Very young caps (plus stipe)<br />

have negligible bioluminescence (5x10' h~/s),<br />

while fresh, mature caps emit 2-3x10~ ~v/s.


32<br />

Long photographic exposures (2-4h) suggested<br />

that the major portion <strong>of</strong> light was emitted<br />

from the gill edges and in some cases from<br />

the hymenopodium. This was confirmed by low<br />

light-level video microscopy. The portion<br />

<strong>of</strong> the luminescent hyphae coincides with the<br />

location <strong>of</strong> the cheilocystidia. In senescing<br />

fruiting bodies 30-60% <strong>of</strong> the tbtal light<br />

emission could be detected from the pileus<br />

after the removal <strong>of</strong> the gills, in agreement<br />

with the observations <strong>of</strong> Buller (1924). In<br />

fresh, mature basidiocarps, however, light<br />

emission from the pileus, after removal <strong>of</strong><br />

the gills was less than 10% <strong>of</strong> that <strong>of</strong> the<br />

gills. The cheilocystidia. which are cytologically<br />

distinct from the basidia, contain<br />

numerous lipid-like granules and. more mitochondria<br />

than are found in other hymenial<br />

cells. Supported by NSF grants PCM82-08534,<br />

BRS82-14960 and NIH grant GM-20829.<br />

D. J. LODGE. Center for Energy and Environment<br />

Research, G.P.O. Box 3682 San Juan, PR 00936.<br />

Colonization <strong>of</strong> eastern cottonwood roots by endo- and<br />

ectomycorrhizal fungi on a dredge spoil island.<br />

Colonization <strong>of</strong> Populus deltoides roots by VAendo-<br />

and ectomycorrhizal fungi was studied on Eagle<br />

Island in Wilmington, North Carolina. Viable<br />

mycorrhizal inoculum was initially absent from the<br />

dredge spoils. The frequency <strong>of</strong> non-mycorrhizal trees<br />

was significantly lower than it would have been if P,<br />

deltoides had only been able to form one type <strong>of</strong><br />

mycorrhizal association. The increased probability<br />

<strong>of</strong> infection associated with the ability to form both<br />

endo- and ectomycorrhizae could have favored the<br />

evolution <strong>of</strong> endo-/ectomycorrhrzal species among<br />

plants which are primary colonizers, assuming that<br />

both groups <strong>of</strong> fungi facilitate plant establishment.<br />

The percentage <strong>of</strong> root length infected by ectomycorrhizal<br />

fungi decreased with distance from the old<br />

forest on one end <strong>of</strong> the island (the nearest source<br />

<strong>of</strong> inoculum), and increased with tree diameter class.<br />

These two variables accounted for 62% <strong>of</strong> the variation<br />

in ectomycorrhizal root length. Endomycorrhlzae<br />

were absent from cottonwoods which were not associated<br />

with other potential hosts <strong>of</strong> endomycorrhzzal<br />

fungi, which suggests that root-to-root contacts may<br />

be important in local spread. The percentage <strong>of</strong> fine<br />

root length infected by endomycorrhizal fungi was<br />

negatively correlated with distance from the nearest<br />

road, which suggests that traffic might have<br />

dispersed soil containing endomycorrhlzal inoculum<br />

along roads. The patterns observed for infection by<br />

endo- and ectomycorrhizal fungi were consistent with<br />

soil-borne and air-borne dispersal, respectively.<br />

A03 *LIi


ferent dikaryons are maintained as individuals are as<br />

follows:<br />

1. I find that dikaryons differing in one or both parent<br />

monokaryons exhibit antagonisms with each other.<br />

I obtained these results using 4 parent monokaryons to<br />

construct all combinations <strong>of</strong> dikaryons.<br />

2. The cytoplasmic (mitochondrial) backround <strong>of</strong> the dikaryons<br />

may mediate these interactions; in fact, a<br />

difference in mitochondrial types alone may be enough<br />

to cause incompatibility.<br />

3. Once formed, dikaryons produced by dikaryoojmonokaryon<br />

matings exhibit antagonism toward the parent<br />

dikaryon.<br />

From these studies, I conclude that continuity <strong>of</strong> mating<br />

colonies, in either sexual process is short-lived.<br />

,in investigation <strong>of</strong> the cytological bases <strong>of</strong> these interactions<br />

is currently underway.<br />

Mayfield, J. E., see Taylor, R., et. al.<br />

McGuinness, M. D., see Haskins, E. F.<br />

M.D. MCGUINNESS and E.F. HASKINS. Department <strong>of</strong><br />

Botany, University <strong>of</strong> Washington, Seattle, WA 98195.<br />

Fultiple alleles at the mating type locus in<br />

Echinostelium coelocephalum.<br />

Four isolates <strong>of</strong> Echinostelium coeloce halum have<br />

been aeneticall v anal vzed for t F--- e presence <strong>of</strong> heterothall<br />

ism. cros;ing experiments involving the parental<br />

generation <strong>of</strong> each isolate have demonstrated they are<br />

all heterothallic. The nature <strong>of</strong> the mating system<br />

in each isolate is a one locus bi-allelic system<br />

similar to that <strong>of</strong> the other myxomycetes thus far<br />

genetically analyzed. When tester clones <strong>of</strong> different<br />

mating types from each isolate were crossed in all<br />

possible pairwise combinations, protoplasmodia were<br />

produced by every cross. These data establish that<br />

each isolate possesses a unique pair <strong>of</strong> mating alleles.<br />

The presence <strong>of</strong> multiple mating alleles in these<br />

isolates <strong>of</strong> E. coelocephelum represents the first<br />

multiple allelic mating system in the myxomycetes<br />

outside the Physarales.<br />

McLaughlin, D. J., see O'Donnell, K. L.<br />

D. J. MCLAUGHLIN and K. L. OIDONNELL. Dept. <strong>of</strong><br />

Botany, University <strong>of</strong> Minnesota, St. Paul, MN 55108.<br />

Nuclear division in the Heterobasidiomycetes: problems<br />

and pros'wcts.<br />

Nuclear division has been inv'kstigated ultrastructurally in<br />

relatively few Heterobasidiomycetes. Many orders remain<br />

unstudied, and a representative sampling <strong>of</strong> the genera in<br />

those orders which have been studied is still lacking. In<br />

the organisms examined a variety <strong>of</strong> spindle pole body<br />

forms and nuclear division features have been revealed<br />

which may clarify the systematics and provide guidance<br />

in interpreting evolution. The following topics will be<br />

discussed: 1, technical problems and advances in<br />

methodology; 2, utility <strong>of</strong> the data, i.e., its limitations<br />

and its predictive value; and , 3, groups or species where<br />

studies are needed or may be especially informative. While<br />

nuclear division studies by themselves may not solve the<br />

problem <strong>of</strong> evolution <strong>of</strong> the Heterobasidiomycetes, they<br />

hold promise as a part <strong>of</strong> the solution.<br />

.C. McMorris, Chemistry <strong>of</strong> Oogoniols, Department <strong>of</strong><br />

Chemistry, University <strong>of</strong> California, San Diego,<br />

La Jolla, California 92093.<br />

Achlya contains many steroids including<br />

fucosterol, 24-methylene cholesterol and cholesterol.<br />

The major steroid fucosterol is the precursor <strong>of</strong><br />

33<br />

antheridiol and deoxyantheridiol in female strains<br />

<strong>of</strong> Achlya and <strong>of</strong> oogoniols in male strains as well,<br />

<strong>of</strong> course, as hermaphroditic strains. At least<br />

eight oogoniols have been identified in culture<br />

liquids <strong>of</strong> Achlya heterosexualis. The steroids<br />

designated oogoniol -1, -2 and -3 are isobutyrate,<br />

propionate and acetate esters <strong>of</strong> the C3 hydroxyl<br />

<strong>of</strong> oogoniol. Each compound was originally thought<br />

to be pure but was later found to be a mixture with<br />

the dehydro analogue.<br />

Thus dehydrooogoniol is the 7-0x0-lla, 158, 29-<br />

trihydroxy derivative <strong>of</strong> fucosterol and retains the<br />

carbon skeleton <strong>of</strong> fucosterol. Biosynthetic evidence<br />

indicates that it is the precursor <strong>of</strong> oogoniol which<br />

is the C24(28) dihydro derivative. The former<br />

compound is about 100 times more active, biologically,<br />

than oogoniol and it may be the true femaleactivating<br />

hormone or pheromone in Achlya. The<br />

significance <strong>of</strong> esterification <strong>of</strong> the C3 hydroxyl<br />

leading to less polar steroids oogoniol-1 etc.,<br />

is unclear since biological activity is not affected.<br />

R.J. MEYER, M. MOHAN, J.B. ANDERSON, and P.A. HORGEN<br />

Dept. Botany, Univ. Toronto, Erindale Campus,<br />

Mississauga, Ontario L5L 1C6. Analysis <strong>of</strong> plasmids<br />

in Agaricus.<br />

Two plasmid-like DNA components are observed when<br />

total DNA from a strain <strong>of</strong> Agaricus bitorquis is<br />

subjected to agarose gel electrophoresis. One is 4<br />

kb in size; the other is 7.5 kb. The 7.5 kb component<br />

consists <strong>of</strong> two distinct plasmids; complete restrictions<br />

generate fragments that add up to 15 kb<br />

(Mohan et al. 1984. Current Genetics 8:615). Our<br />

goal is to clone each <strong>of</strong> the Agaricus plasmids in a<br />

bacterial plasmid vector for use in further<br />

studies. To date we have cloned several EcoRl restriction<br />

fragments <strong>of</strong> pEMl into pUC18 and used the<br />

recombinant plasmids as probes against mitochondrial<br />

and plasmid DNA preparations from various strains <strong>of</strong><br />

- A. bitorquis and A. brunnescens.The data collected<br />

supports the earlier interpretation <strong>of</strong> Mohan et al.<br />

. ~estriction maps <strong>of</strong> pEMl and pEM2 have<br />

been constructed by analysis <strong>of</strong> partial restrictions.<br />

In spite <strong>of</strong> their different restriction<br />

sites, pEMl and pEM2 have some homology, at least<br />

under the stringency used thus far. No homology has<br />

been observed between one <strong>of</strong> the cloned fragments<br />

and mitochondrial DNA, which suggests that the plasmids<br />

are not simply fragments <strong>of</strong> the mitochondrial<br />

genome. No homology has been detected between one<br />

<strong>of</strong> the cloned fragments and other plasmids in different<br />

strains<strong>of</strong> fi. bitorquis. Studies with other<br />

cloned fragments <strong>of</strong> pEkl and pEM2 will also be<br />

reported.<br />

----<br />

S. L. F. MEYER and M. C. HEATH. Botany Dept.,<br />

Univ. <strong>of</strong> Toronto, Toronto, Ontario M5S 1Al.<br />

Comparison <strong>of</strong> chemically-induced and fungal-induced<br />

cell death in epidermal cells <strong>of</strong> cowpea.<br />

The objectives <strong>of</strong> this study were 1) to determine<br />

if stages occur during plant cell death that can be<br />

identified by light microscopy, 2) to see whether<br />

fungal-induced cell death includes stages similar<br />

to those that occur when cell death is caused by a<br />

nonliving agent, and 3) to correlate stages<br />

observed by light microscopy with ultrastructural<br />

features <strong>of</strong> the dying cells. The abiotic factor<br />

used to kill cells was copper chloride. The stages<br />

in the death process that it initiated in cowpea<br />

epidernal cells included slowing and cessation <strong>of</strong><br />

cytoplasmic streaming, morphological changes in the<br />

cytoplasm such as the appearance <strong>of</strong> "bubbles", and<br />

shrinkage <strong>of</strong> protoplasts. The morphological


34<br />

features seen by light microscopy were reflected in<br />

the distinctive ultrastructural appearance <strong>of</strong> the<br />

cytoplasm. Studies are underway to compare this<br />

chemically-induced cell death with death induced in<br />

the same cell type by Cochliobolus heterostrophus<br />

Race 0, a non~athonen <strong>of</strong> cowDeas that ~enetrates<br />

and kills epiderrnai cells. A<br />

Miller, Jr.. 0. K., see Flynn, T. M.<br />

Miller, 0. K., Jr., see Vilgalys, R.<br />

Miller, 0. K., Jr., see Vilgalys, R., et. al.<br />

STEVEN L. m. Department <strong>of</strong> Biology, Virginia<br />

Polytechnic Institute and State University, Blacksburg,<br />

VA 24061. Early basidiosporogenesis and spore release<br />

mechanisms in the gasteroid and agaricoid Russulales.<br />

Ballistosporic discharge appears to be a conservative<br />

phenomenon in most basidiomycetes, resulting from a<br />

prescribed sequence <strong>of</strong> biochemical and developmental<br />

processes. Ultrastructural characterization <strong>of</strong><br />

sterigma formation, spore orientation and development,<br />

and spore release mechanisms may provide valuable<br />

systematic information to aid the understanding <strong>of</strong><br />

evolution in the basidiomycetes. Morphologically and<br />

ecologically the Russulales are a homogeneous group.<br />

However, this order contains both ballistosporic and<br />

statismosporic, agaricoid and gasteroid taxa. Spore<br />

symmetry and ability to forcibly discharge spores are<br />

therefore fundamental systematic characteristics, yet<br />

ballistosporic and statismosporic basidiosporogenesis<br />

has not been critically examined. Early<br />

basidiosporogenesis, spore-wall tegumentation, and<br />

differentiation <strong>of</strong> the hilar appendix were<br />

ultrastructurally compared in eight genera <strong>of</strong> agaricoid<br />

and gasteroid Russulales. Six layers were present in<br />

all developing spores, two <strong>of</strong> which were associated<br />

with an evanescent pellicle and four were derived from<br />

the sterigma and young spore. Ontogeny <strong>of</strong> spore-wall<br />

ornamentation was similar in all genera, however<br />

diversity in the degree <strong>of</strong> ornamentation resulted from<br />

differentiation <strong>of</strong> the four enduring wall layers.<br />

Developmental anatomy associated with spore release<br />

mechanisms was also examined. Systematic implications<br />

<strong>of</strong> basidiosporogenesis in the evolution <strong>of</strong> the<br />

Russulales and other secotioid and gasteroid<br />

basidiomycetes will be discussed.<br />

STEVEN L. MILLER. Department <strong>of</strong> Biology, Virginia<br />

Polytechnic Institute and State University,<br />

Blacksburg, VA 24061. Ectomycorrhizae in the<br />

Russulales-a systematic interpretation.<br />

The morphology and anatomy <strong>of</strong> ectomycorrhizae reflect<br />

many characteristics present in the fruiting<br />

structures and vegetative mycelium <strong>of</strong> a particular<br />

fungal symbiont. In addition, ectomycorrhizae may<br />

possess characteristics which are not present in the<br />

fungus alone or are ignored in the taxonomy and<br />

systematics <strong>of</strong> the fungus. Ectomycorrhizal<br />

morphology has not been used to evaluate the<br />

systematic position <strong>of</strong> a particular taxon or group <strong>of</strong><br />

ectomycorrhizal fungi.<br />

Ectomycorrhi zae <strong>of</strong> several genera <strong>of</strong> gasteroid and<br />

agaricoid Russulales were synthesized in the<br />

laboratory using the growth-pouch technique.<br />

Mycel ial plugs were used as the source <strong>of</strong> inoculum.<br />

Mantle morphology and anatomy were compared using<br />

one micrometer thick cross and longitudinal plastic<br />

sections. Sulfo-aldehyde staining <strong>of</strong> the ectomycorrhizal<br />

root1 ets indicated the presence <strong>of</strong> sesquiterpenoid<br />

lactones. Lateral rootlets showed a tendency<br />

to grow toward the inoculum plugs, contact the plugs<br />

and become ectomycorrhizal. The implications <strong>of</strong><br />

ectomycorrhizal formation, ectomycorrhizal morphology<br />

and anatomy, and host lateral root behavior in the<br />

evolution <strong>of</strong> the Russulales will be discussed.<br />

C.W. MIMS ano N.L. NICKERSON. Department <strong>of</strong> Biology,<br />

Stephen F. Austin State University, Nacogdoches,<br />

TX 75962, and Research Station, Agriculture Canada,<br />

Kentville, Nova Scotia, B4N 155. Ultrastructure <strong>of</strong><br />

the host-pathogen relationship in red leaf disease<br />

<strong>of</strong> lowbush blueberry.<br />

Red leaf disease <strong>of</strong> blueberry is caused by the basidiomycetous<br />

fungus Exobasidium vaccinii Wor. This<br />

fungus produces a p e m e l i u m that invades the<br />

rhizomes <strong>of</strong> Vaccinium angustifolium Ait. Symptoms<br />

are seen on infected shoots soon after buds break in<br />

the spring and the reddish leaves for which the<br />

disease is named soon become apparent. In this<br />

study TEM was used to examine the host-pathogen<br />

relationship in infected leaves.<br />

Exobasidium vaccinii produced a system <strong>of</strong> slender,<br />

branched, septate hyphae within infected leaves.<br />

Although hyphae were routinely observed within cells<br />

<strong>of</strong> the lower epidermis, elsewhere hyphae grew almost<br />

exclusively in an intercellular fashion. Hyphae typically<br />

filled the intercel lular spaces near the<br />

lower epidermis but were rather sparse elsewhere<br />

in the leaf. The haustorial apparatus consisted <strong>of</strong><br />

short, finger-like or lobed structures that arose<br />

from intercellular hyphae in close association with<br />

host cells. Each haustorium contained distinctive<br />

membranous inclusions and had one or more electronopaque<br />

haustorial caps. Haustoria usually appeared<br />

to be ensheathed by host cell wall material although<br />

some haustorial caps appeared to penetrate the host<br />

wall.<br />

Mohan, M., see Meyer, R. J., et. al.<br />

Molina, R., see Castellano, M. 4.<br />

GARETH MORGAN-JONES. Department <strong>of</strong> Botany,<br />

P l a n t P m g y Microbiology, Auburn<br />

University, ~iabama 36849. ~oncerni ng<br />

Dia orthe phaseolorum f.sp. caulivora, and<br />

-!+-<br />

sov ean stem canker in the southeastern<br />

~n?ted States.<br />

Incidence <strong>of</strong> soybean stem canker has greatly<br />

increased in the southeastern U.S. during<br />

the last five years and losses<br />

*<br />

from the disease<br />

are estimated at over 40 million dollars.<br />

Southeastern biotypes <strong>of</strong> g. haseol orum f. sp.<br />

caulivoia, which have the abi ity to kill the<br />

soybean plant well before harvest, differ<br />

from northern isolates in cultural characteristics<br />

in vitro, including colony appearance<br />

and color, growth rate at different temperatures,<br />

stroma size and perithecial and ascospore<br />

morphology. Some differences in morphology<br />

<strong>of</strong> the anamorphic Phomo sis state,<br />

particularly conidiophore 77- ranching, are also<br />

evident between southeastern and northern<br />

isolates. These facts, together with data<br />

from host inoculation experiments, using<br />

several soybean cul tivars, indicate that a<br />

separate, easily distinguishable, forma<br />

speciales exists in the s0utheast.r<br />

symptoms induced by this organism are demonstrated<br />

and an account given <strong>of</strong> its morphology


Motta, J. J., see Cohen, S. D.<br />

G. M. MUELLER', J. F. AMMIRATI, and L. SHIH, Dept.<br />

3 Etany, Field Museum <strong>of</strong> Natural Hist., Chicago,<br />

IL 60605-2496 and Dept. <strong>of</strong> Botany, U. <strong>of</strong> Washington,<br />

Seattle, WA 98195. Intra- and Intercontinental<br />

pairing studies in Laccaria (Agaricales).<br />

The study <strong>of</strong> incompatibility groups within species<br />

<strong>of</strong> Laccaria from Sweden by Nils Fries and Greg<br />

~ueller revealed a close correlation between<br />

taxonomic species and biological species. It was<br />

unclear, however, if similar results could be<br />

obtained when using isolates from a larger and more<br />

diverse geographical area. Studies pairing Laccaria<br />

isolates from Sweden with those from east=<br />

western U.S.A. have established that, at least in<br />

some cases, taxonomic species from both sides <strong>of</strong> the<br />

Atlantic are compatible on the basis <strong>of</strong> clamp<br />

connection formation when grown in the laboratory.<br />

Also, preliminary pairing studies using North<br />

<strong>America</strong>n isolates <strong>of</strong> L. laccata have not uncovered<br />

additional incompati6ilityoups beyond the two<br />

reported by these workers. This suggests that,<br />

unlike certain other morphologically variable<br />

taxonomic species (e.g., Armillaria mellea) in which<br />

numerous incompatibility groups h a v e detected,<br />

- L. laccata probably consists <strong>of</strong> relatively few<br />

incompati6il ity groups. These studies support using<br />

such a study regime in Laccaria. While such a<br />

comprehensive pairing study is impractical in genera<br />

with large numbers <strong>of</strong> species, pairing studies may<br />

prove useful within species complexes.<br />

lprevious address: Dept. <strong>of</strong> Botany, U.<br />

Seattle. WA 98195<br />

<strong>of</strong> Washington<br />

J. T. MULLINS. Department <strong>of</strong> Botany, University <strong>of</strong><br />

Florida. Gainesville, FL 32611. Carbohydrate<br />

hydrolases and morphogenesis in Achlya.<br />

Endocellulase (1,4-beta-D-Glucan-4-glucanohydrolase,<br />

EC 3.2.1.4) has been implicated in the regulation <strong>of</strong><br />

growth and development <strong>of</strong> Achlya ambisexualis Raper,<br />

via modifications in the structural integrity <strong>of</strong> the<br />

cellulose component <strong>of</strong> the hyphal wall. The induction<br />

and secretion <strong>of</strong> endocellulase into the culture medium<br />

is required for hyphal tip growth (Canad. J. Bot.<br />

57:2145, 1979) and for hormonally induced branching<br />

(Physiol. Plant. 22:347, 1969; Tissue & Cell 11:585,<br />

1979). Fungi capable <strong>of</strong> growing on cellulose exhibit<br />

three associated enzyme activities: (1) the endocellulase;<br />

(2) 1,4-Beta-D-glucan cellobiohydrolase (EC<br />

3.2.1.91); and (3) Beta-glucosidase (EC 3.2.1.21). The<br />

cooperative action <strong>of</strong> these three enzymes is required<br />

for the complete hydrolysis <strong>of</strong> cellulose to glucose. In<br />

Achlya, where cellulase functions in morphogenesis,<br />

only one <strong>of</strong> these activities (the endocellulase) is<br />

expressed. Thus it is distinctively different from the<br />

enzymes found in those fungi which grow on cellulose.<br />

The beta-glucosidase when functoning in a cel lulase<br />

complex, hydrolyzes cellobiose to glucose and is thus a<br />

cellobiase. In Achlya the beta-glucosidase will not<br />

cleave cellobiose, but instead hydrolyzes a storage<br />

cytoplasmic glucan. It is also active against<br />

laminaribiose .<br />

Nickerson, N. L., see Mims, C. W.<br />

Noga, E. J., see Dykstra, M. J.<br />

F. OBERWINKLER, Lehrstuhl Spezielle Botanik,<br />

Universitat Tubingen, Auf der Morgenstelle 1<br />

D-7400 Tubingen, West Germany.<br />

Mycoparasitic Heterobasidiomycetes.<br />

The majority <strong>of</strong> mycoparasitic Basidiomycetes<br />

are represented by the Heterobasidiomycetes.<br />

They occur in the auriculariaceous genera<br />

Cystobasidium, Platygloea, and Mycogloea,<br />

the tremellaceous genera Tremella, Tetragoniomyces,<br />

Trimorphomyces, and Xenolachne,<br />

and in the holobasidiate genera Carcinomyces,<br />

Christiansenia, and Syzygospora. The<br />

taxonomy <strong>of</strong> these taxa is discussed. Several<br />

mycoparasitic species develop conspicuous<br />

basidiocarps, but most species have tiny<br />

fructifications. Some parasites occur intrahymenially,<br />

i.e. they develop basidia<br />

and/or conidia within the hymenia <strong>of</strong> the<br />

host fungi. There are examples for which it<br />

is doubtful whether they represent parasites<br />

or saprobes.<br />

The ultrastructural differentiations <strong>of</strong> cell<br />

interactions between parasites and hosts<br />

vary considerably, as is demonstrated in<br />

Platygloa peniophorae and Tremella mycophais-<br />

Mycoparasitism <strong>of</strong> Heterobasidiomycetes is<br />

compared with that <strong>of</strong> Homobasidiomycetes and<br />

with parasitism <strong>of</strong> basidiomycetes on plants.<br />

K. L. O'DONNELL and D. J. MCLAUGHLIN. Department<br />

<strong>of</strong> Botanv. University <strong>of</strong> Minnesota. St. Paul, MN 55108.<br />

Nuclear bivision in the ~stila~inackae and ~illetiaceae.<br />

Taxonomic treatments <strong>of</strong> the Ustilaginaceae (smuts) and<br />

Tilletiaceae (bunts) are undoubtedly influenced by the<br />

strong probability <strong>of</strong> convergence (i.e., encysted probasidia<br />

or teliospores and passive basidiospore liberation) as well<br />

as their importance as plant pathogens (Wells 1982). This<br />

study was initiated to evaluate the phylogenetic<br />

relationship <strong>of</strong> these taxa within the Basidiomycota.<br />

Details <strong>of</strong> nuclear division appear to be evolutionarily<br />

conservative; therefore, spindle pole body form and cycle,<br />

and nuclear envelope and nucleolar behavior (Taylor 1983)<br />

together with other mitotic characters (Heath 1980) <strong>of</strong>fer<br />

the potential for evaluating the connection between the<br />

Tilletiales s. str. and Ustilaginales s. str. (Oberwinkler<br />

1982) and other basidiomycetous taxa. Nuclear events in<br />

selected species were examined during basidial and<br />

basidiospore ontogeny and secondary spore andlor yeastlike<br />

cell formation by light microscopy and electron<br />

microscopy. Electron microscopic analysis employed the<br />

freeze-substitution technique (Howard and Aist 19791,<br />

where possible, to minimize fixation artifacts (Thielke<br />

1982) together with selection <strong>of</strong> individual cells from flat<br />

embedments for subsequent serial section analysis.<br />

Preliminary results provide support for some phylogenetic<br />

hypothesis.<br />

O'Donnell, K. L., see McLaughlin, D. J.<br />

O'Kane, D. J., see Lingle, W. L., et. al.<br />

Ovrebo, C. L., see Cibula, W. G.<br />

D. PEKKALL and J.C. SILVER. Department <strong>of</strong><br />

Microbiology, University <strong>of</strong> Toronto, West Hill,<br />

Ontario, Canada. M1C 1A4. Changes in ribosomal<br />

protein phosphorylation during heat shock <strong>of</strong> the<br />

filamentous fungus Achlya ambisexualis.<br />

Heat shock in the fungus Achlya ambisexualis<br />

resulted in a rapid reduction in the rate <strong>of</strong> total


36<br />

protein synthesis followed by a slight increase<br />

(to 30% <strong>of</strong> control levels) at the time that heat<br />

shock proteins were detected. When proteins from<br />

500 mM KC1-dissociated ribosomes from 32~-labeled<br />

control (28'C) and heat-shocked (37.C) cells were<br />

analysed by SDS gel electrophoresis and autoradiography,<br />

several major changes in the phosphorylation<br />

<strong>of</strong> ribosome-associated proteins were seen.<br />

A basic 30 Kd small ribosomal subunit protein highly<br />

phosphorylated in controls exhibited markedly<br />

decreased 32~-labelling after heat shock. This<br />

protein may be analogous to mammalian ribosomal<br />

protein S6. In those ribosomes which were stable<br />

in 500 mM KC1, however, decreased labelling <strong>of</strong> the<br />

30 Kd protein during heat shock was not detected.<br />

This observation suggests that changes in ribosomal<br />

protein phosphorylation may be different in<br />

ribosomes active in protein synthesis and in those<br />

which are inactive. Heat shock also induced a<br />

marked increase in the 32~-labelling <strong>of</strong> a 32 Kd<br />

protein and a marked decrease in the 32p-labslling<br />

<strong>of</strong> a 50 Kd protein. These proteins may be<br />

initiation or elongation factors and their<br />

modification may be involved in the rapid changes<br />

observed in the rate <strong>of</strong> protein synthesis during<br />

heat shock.<br />

(Supported by NSERC, Canada)<br />

Pekkala, D., see Silver, J. C.<br />

Pendergrass, L, see Frederick, L., et. al.<br />

J. C. PENDLAND and D. G. BOUCIAS. Department<br />

<strong>of</strong> Entomology and Nematolo@y, University <strong>of</strong> Florida,<br />

Gainesville, FL 32611.<br />

Lectin-binding characteristics <strong>of</strong> several<br />

entomogenous hyphomycetes.<br />

The hyphomycetous insect pathogens, Nomuraea<br />

rileyi, Paecilowces farinosus - ATCC 2b319,<br />

Meta~hizium anisopliae and Beauveria bassiana were<br />

tested with FITC labeled lectins. Concanavalin A,<br />

specific for glucose and mannose residues, bound to<br />

cell walls (hyphal body and/or mycelium) <strong>of</strong> all<br />

fungi examined. Soybean and wheat germ agglutinins<br />

(affinities for 8-acetylgalactosamine and<br />

N-acetylglucosamine, respectively) bound<br />

inconsistently to some cell wall areas.<br />

Peanut<br />

agglutinin, specific for galactose residues, bound<br />

to walls <strong>of</strong> only 2. farinosus and B. bassiana.<br />

Knowledge <strong>of</strong> the composition <strong>of</strong> fungal surface<br />

residues may be important with respect to insect<br />

defense mechanisms against the invading cells.<br />

Lectins produced by insects (e-g. Anticarsia<br />

gemmatalis) are known to be specifically inhibited<br />

by galactose (or higher concentrations <strong>of</strong> glucose).<br />

Fungal cells (P. farinosus, E. bssiana)a which<br />

bear exposed galactose residues as detected by<br />

FITC peanut agglutinin appear to be especially<br />

efficient in removing hemagglutination activity<br />

from Anticarsia hernolymph indicating absorption <strong>of</strong><br />

this insect lectin to fungal surfaces.<br />

J. L PITT, K. A. WHEELER and A. D. HOCKING. CSIRO<br />

Divn <strong>of</strong> Food Research, P.O. Box 52, North Ryde N.S.W.<br />

2113, Australia Fungi from Indonesian dried fish<br />

Involvement in a project on fish drying in the tropics provided<br />

the opportunity to survey the occurrence <strong>of</strong> spoilage<br />

and other fungi in salted and dried fish in Indonesia<br />

About 50 samples <strong>of</strong> a variety <strong>of</strong> fish types have been examined.<br />

As was to be expected, Eurotium and Aspergillus<br />

species were frequently encountered. Other results were<br />

surprising, for example the total absence <strong>of</strong> the I1dunt1<br />

mould Wallemia sebi, traditionally regarded as the principal<br />

cause <strong>of</strong> spoilage <strong>of</strong> salt fish Equally unexpected was<br />

that the dominant spoilage fungus was an undescribed species,<br />

which we have named Polypaecilum w. Other significant<br />

spoilage fungi included Eurotium spp, Aspergillus<br />

penicilloides and Basipetospora halophila (= Scopulariopsis<br />

halophilica). The number and variety <strong>of</strong> Penicillia encountered<br />

from a tropical environment was also surprising, and<br />

these included several new species. Known mycotoxigenic<br />

fungi were isolated only in low numbers. Preliminary<br />

studies on factors influencing growth <strong>of</strong> these fungi, especially<br />

water activity, temperature and NaCl concentration,<br />

will also be discussed.<br />

J. POMMERVILLE, K. HARDING, and B. STRICKLAND.<br />

The Departments <strong>of</strong> Biology and Chemistry, Texas A&M<br />

Univers~ty, College Station, TX 77843. Slrenin analogs for<br />

the study <strong>of</strong> receptor recognition during male gamete<br />

chemotaxis in Allomyces.<br />

Sirenin, the sexual pheromone <strong>of</strong> the aquatic fungus,<br />

Allomyces macrogynus (Burma 3-35), is produced by female<br />

gametes and acts as an attractant for the male gametes.<br />

In order to better understand the nature <strong>of</strong> thls<br />

communication system, we have synthesized and examined<br />

by chemotactic assay the structure <strong>of</strong> several sirenin<br />

analogs several <strong>of</strong> which exhibit strong male attraction.<br />

The synthesis <strong>of</strong> a dl01 compound containing the blcyclic<br />

structure <strong>of</strong> sirenin but lacking a hydroxymethyl group on<br />

the SIX-membered ring, exhibited activity comparable to<br />

natural slrenln. This led us to test structures lacking the<br />

b~cyclic structure but possessing the diol relationship <strong>of</strong><br />

the above compound. Such diols were found to be qulte<br />

active, demonstrating that the bicyclic structure is not<br />

necessary for chemotact~c activity. From the results <strong>of</strong><br />

other compounds tested, ~t is evident that the structural<br />

requirements <strong>of</strong> the receptor site can be met by molecules<br />

with structures varying considerably from the structure <strong>of</strong><br />

natural sirenin. The evidence suggests that the synthetic<br />

diols are active because the two hydroxyl groups can bind<br />

to the receptor site in the same manner as the two<br />

hydroxyl groups in sirenin. Such preliminary studles will<br />

make it possible to determine in detail the spec~ficity <strong>of</strong><br />

the receptor sites, examine the mechanisms <strong>of</strong> pheromone<br />

inactivation by the male gametes, and investigate the<br />

location, number, and nature <strong>of</strong> the receptor sltes.<br />

Pommerville, J., see Aliaga, 6. R.<br />

Pommerville, J., see Sewall, T.<br />

Porter, D., see Lingle, W. L., et. al.<br />

Poth, M. A., see Dunn, P. H., et. al.<br />

Radford, P. T., see Blackwell, M., et. al.<br />

S.A. REDHEAD and J.H. GINNS. Biosystematics fiesearch<br />

Institute, Agricult~ire Canada, Ottawa, Ont., Canada,<br />

KIA OC6.<br />

Agaric geners causing brown rots.<br />

Relatively Few species <strong>of</strong> agarics are capable <strong>of</strong><br />

causing a brown rot <strong>of</strong> wood. Species in the genera<br />

Coprinus, Hygrophoropsis, Hypsizygus, Lentinus,<br />

and Paxillus have been considered brown rotters.<br />

The aSility to cause a brown rot is a generic<br />

feature in tile aphyllophorales in refined<br />

taxonomic schemes correlating this physiological


character with morphological or anatomical<br />

characters. A reevaluation <strong>of</strong> the list <strong>of</strong> brownrot<br />

agaric qenera resu1.ted in the removal <strong>of</strong><br />

Coprinus as suspect, and the exclusion <strong>of</strong> Lentinus<br />

sensu stricto and Paxillus sensu stricto. Two<br />

new genera, Neolentinus and Heliocybe, are proposed<br />

for :,rown-rot species formerly treated in Lentinus,<br />

and a third new genus, Ussicaulis, for one<br />

previously considered to be a Pleurotus. The<br />

brown-rot genus Tapinella is resurrected as a<br />

link between the hrown-rot family Coni~phoraceae<br />

and the mycorrhizal genus Paxillus, both in<br />

the order Roletales. Recognition <strong>of</strong> the white-rot<br />

genus Lentinula for the Shiitake and allies is<br />

sl~pported I))( decay studies. Six genera <strong>of</strong><br />

agaricoid hyrnenomycetes in at least two orders<br />

now arc consider~d to be brown-rot taxa. Among<br />

agaric genera the formation <strong>of</strong> a brown-rot is a<br />

qerler I c rea t :re.<br />

DON R. REYNOLDS. Natural History Museum,<br />

n o Exposition Boulevard, Los Angeles,<br />

California 90007.<br />

A phylogenetic view <strong>of</strong> the Capnodiaceae<br />

sensu lato.<br />

The Capnodiaceae sensu lato is analyzed<br />

with cladistic technique. The hypothesis<br />

being tested is that the sexual states<br />

and the asexual states <strong>of</strong> monophyletic<br />

pleoholomorphs will have similar trees.<br />

ROBERT H. RIEHL* AND DAVID 0. TOFT. Department <strong>of</strong><br />

Cell Biology, Mayo Clinic, Rochester, MN, 55950. The<br />

Antheridiol Receptor <strong>of</strong> Achlya ambisexualis E87.<br />

We have detected a high affinity bindinz protein<br />

in the cytosol <strong>of</strong> A. ambisexualis male cells ;hat is<br />

specific for antheridiol and a tritium-labeled<br />

analog. Studies have revealed that, in the presence<br />

<strong>of</strong> sodium molybdate, this macromolecule has a<br />

sedimentat ion coefficient <strong>of</strong> 8.3s in sucrose<br />

gradieqts <strong>of</strong> low ionic strength, a Stokes radius <strong>of</strong><br />

56.6 A (Sephacryl 5-300 columns), a molecular<br />

weight <strong>of</strong> approximately 192,000, a frictional ratio<br />

<strong>of</strong> 1.5, and an axial ratio <strong>of</strong> 8.9. The binding<br />

protein can be eluted with 0.24 M KC1 as a single<br />

peak from DEAE-Sephadex A-25 columns. When sucrose<br />

gradients are prepared containing 1 M KC1 without<br />

molybdate, a shift in sedimentation c.oefficient from<br />

8.3s to 3.6s occurs. Recently, we have produced a<br />

monoclonal antibody to one component <strong>of</strong> ,the<br />

antheridiol receptor that cross-reacts with a similar<br />

component <strong>of</strong> the steroid receptors <strong>of</strong> birds and<br />

mammals. These results indicate that this steroid<br />

binding protein from Achlya has in vitro biochemical<br />

properties that are similar to those <strong>of</strong> the steroid<br />

receptors in other organisms and that these<br />

properties may have been evolutionarily conserved.<br />

ROBERT W. ROBERSON, E. S. LUTTRELL, Department <strong>of</strong><br />

Plant Pathology, University <strong>of</strong> Georgia, Athens, GA<br />

30602, and NORMA L. CASHION, formerly CIMMYT. Londres<br />

40, Apdo. Postal 6-641, 06600 Mexico. D.F. Formation<br />

<strong>of</strong> exogenous terminal teliospores in Neovossia indica<br />

(Tilletiaceae).<br />

Teliospores <strong>of</strong> the karnal bunt fungus, Neovossia<br />

indica, develop in extensive shallow cavities<br />

resulting from dissolution <strong>of</strong> the middle layers <strong>of</strong><br />

the pericarp <strong>of</strong> the wheat grain. The cavity is<br />

bounded on the outside by the epidermal and hypodermal<br />

layers <strong>of</strong> the pericarp and on the inside by<br />

the layer <strong>of</strong> cross cells and tube cells. The intercellular<br />

hyphae <strong>of</strong> the fungus line the cavity with a<br />

hymenium-like stroma <strong>of</strong> compacted cells. Short hyphal<br />

37<br />

branches arising from generative cells ir~ the stromal<br />

layer project into the cavity. The tips <strong>of</strong> these<br />

sporogenous branches swell into pyriform teliospore<br />

initials. The primary wall <strong>of</strong> the spore is continuous<br />

with the wall <strong>of</strong> the sporogenous hypha. As the protoplasm<br />

<strong>of</strong> the sporogenous hyphae moves toward its tip<br />

a series <strong>of</strong> empty cells is cut <strong>of</strong>f by septa, and a<br />

final septum delimits the binucleate spore initial.<br />

The two nuclei Fuse and the initial expands enormously<br />

into the globose spiny teliospore. This type<br />

<strong>of</strong> development contrasts with the endogenous formation<br />

<strong>of</strong> teliospores in intercalary hyphal cells with<br />

swollen gelatinous walls reported in Ustilaginaceae..<br />

R.G. ROBERTS. Field and Horticultural Crops Research<br />

Unit, USDA:ARS, R. B. Russell Agricultural Research<br />

Center, P. 0. Box 5677, Athens, GA 30613.<br />

The anamorph <strong>of</strong> Microascus intermedius Emmons & Dodge<br />

During myc<strong>of</strong>loral studies <strong>of</strong> sunflower seeds, an<br />

ascomycete morphologically indistinguishable from<br />

Microascus intermedius was frequently isolated from<br />

low quality seeds. Von Arx erected the genus<br />

Pithoascus for g. nidicola, g. intermedius and other<br />

species lacking anamorphs, with no ascospore germ<br />

pores and with papillate ascomata. The sunflower<br />

isolates <strong>of</strong> M. intermedius were consistently associated<br />

with an undescribed Scopulariopsis anamorph,<br />

especially when grown on sunflower seeds. Conidia<br />

were globose to subglobose, hyaline and measured<br />

4-6(8) X 4-5.5(7.5) micrometers. Annelides measured<br />

4-13 X 2-2.5 micrometers. Fungus-free sunflower<br />

seeds inoculated with ascospores <strong>of</strong> g. intermedius<br />

consistently produced both the anamorphic and teleomorphic<br />

states. Conidial isolates consistently produced<br />

cultures with fertile ascomata <strong>of</strong> g.<br />

intermedius. Both papillate and rostrate ascomata <strong>of</strong><br />

- M. intermedius and g. intermedius were observed in<br />

culture. The identity <strong>of</strong> 8. intermedius was confirmed<br />

by comparison with the type culture <strong>of</strong> g.<br />

intermedius, which is derived from Emmons and Dodge's<br />

original isolate. In light <strong>of</strong> this study, the<br />

acceptance <strong>of</strong> the genus Pithoascus and the family<br />

Pithoascaceae should be re-examined .<br />

Rogers, J. D., see Glawe, D. 4.<br />

Romaine, C. P., see Wach, M. P., et. al.<br />

Romano, M. A., see Gessner, R. V., et. al.<br />

Ross, I. K., see Kerrigan, R. W.<br />

I. K. Ross, H. T. Choi, and R. L. Wilks. Dept. <strong>of</strong><br />

Biological Sciences, University <strong>of</strong> California, Santa<br />

Barbara, CA 93106. sclerotia and phenoloxidase production<br />

in liquid cultures <strong>of</strong> Coprinus congregatus.<br />

The lack <strong>of</strong> uniformity <strong>of</strong> mycelial balls (pellets)<br />

growing in liquid shake culture is well known, but<br />

usually consists <strong>of</strong> physiological differences among<br />

populations <strong>of</strong> relatively similar cells <strong>of</strong> different<br />

ages and environmental conditions. Such cultures <strong>of</strong><br />

higher fungi are not normally known to undergo differentiation<br />

to form structures composed <strong>of</strong> cells <strong>of</strong><br />

different type and function. On agar cultures, 5.<br />

congregatus may form either mushrooms or sclerotia.<br />

The initial development <strong>of</strong> the early stages <strong>of</strong> both<br />

mushrooms and sclerotia are virtually identical aggregations<br />

<strong>of</strong> hyphae and are probably governed by the<br />

same genetic and biochemical pathways. Phenoloxidases<br />

have been implicated in the first light response <strong>of</strong><br />

- C. congregatus and are now known to be associated with<br />

the very early stages <strong>of</strong> primordium formation. This<br />

oaDer reports the development <strong>of</strong> well-defined scler-


38<br />

.otia in liquid shake cultures and the association with<br />

the format ion <strong>of</strong> the sclerotia <strong>of</strong> developmentally<br />

regulated phenoloxidases. The phenoloxidase associated<br />

with the hyphal tip light response appears to be<br />

different from those associated with sclerotial formation.<br />

Since sclerotia and primordia may share the<br />

same pathways, and phenoloxidases are associated with<br />

both kinds <strong>of</strong> development, the liquid shake culture<br />

system may be a convenient method for studying the<br />

regulation <strong>of</strong> the earliest stages <strong>of</strong> morphogenesis in<br />

this fungus.<br />

A. Y. ROSSMAN. Mycology Laboratory, Plant Protection<br />

Institute, U.S. Oepartment <strong>of</strong> Agriculture, Be1 tsville<br />

Agricultural Research Center, Be1 tsville, Maryland<br />

20705. Recent developments at the National Fungus<br />

Collections.<br />

The National Fungus Collections houses almost one<br />

mill ion fungal specimens comprising the largest<br />

mycological herbarium in the world. In the last<br />

several years the Alexopoulos myxomycetes have been<br />

acquired, curated by Or. M. L. Farr, and incorporated<br />

into the general myxomycete collection which now<br />

consists <strong>of</strong> about 40,000 specimens. Initially in<br />

several parts, the Ames herbarium has been organized<br />

and is available for loan. The herbarium <strong>of</strong> Walter<br />

Snell, acquired in 1980, has now been incorporated<br />

into the general collections. Although housed<br />

separately up to now, the herbarium <strong>of</strong> West Virginia<br />

University will be incorporated shortly. The rare<br />

books <strong>of</strong> the John Stevenson Reference Room have been<br />

cleaned and oiled for preservation, damaged bindings<br />

have been reparied, and pamphlets reorganized.<br />

Roth, I. L., see Frederick, L., et. al.<br />

D. J. ROYSE. Department <strong>of</strong> Plant Pathology, Mushroom<br />

Research Center, 211 Buckhout Laboratory, The<br />

Pennsylvania State University, University Park, PA<br />

16802. Use <strong>of</strong> isozyme variation for cell line<br />

identification, homokaryon detection and hybrid<br />

confirmation <strong>of</strong> cultivated mushrooms.<br />

Most electrophoretic studies <strong>of</strong> fungi have focused<br />

primarily on general protein patterns, using some<br />

specific enzymes. The electrophoretic phenotypes<br />

were evaluated on the presence or absence <strong>of</strong> particular<br />

bands. Other workers, however, postulated genetic<br />

bases for the specific enzyme phenotypes observed.<br />

This latter type <strong>of</strong> approach provides far more information<br />

on genetic variability and its inheritance.<br />

Applications for genetic-based isozyme electrophoresis<br />

in selective breeding programs for edible mushrooms<br />

include: cell line authentication, homokaryon detection,<br />

and hybrid confirmation. Cell line authentication<br />

can be accomplished by assessing specific<br />

alleles at specific loci. Genotypic classes <strong>of</strong> isolates<br />

can be recognized by a series <strong>of</strong> loci having<br />

electrophoretic phenotypes with interpretable genetic<br />

bases. For examole. . , in the common cultivated mushroom,<br />

Agaricus brunnescens, over 20,000 genotypic<br />

classes may be recognized on the basis <strong>of</strong> possible<br />

genotypes from the allelic variability exp;essed at<br />

six polymorphic loci. Incorporation <strong>of</strong> breeding stock<br />

genomes into a single hypha can be confirmed by<br />

dimeric enzymes. Mycelial mixtures <strong>of</strong> parental breeding<br />

stocks are easily differentiated from crosses.<br />

The heterodimer can only be produced when both alleles<br />

are present in their separate nuclei in the same<br />

mycelium.<br />

NITIN SAKSENA and H.H.S. Tripathi. Department <strong>of</strong><br />

Botany, Univeristy <strong>of</strong> Saugar, Sagar (M.P.) 470 003,<br />

India.<br />

Fungistatic activity <strong>of</strong> Trichoderma volatiles against<br />

plant pathogens.<br />

The effect <strong>of</strong> volatitles from six cultures <strong>of</strong> Tricho-<br />

derma (L aureoviride, L, harzianum, T. lon ibrachi-<br />

atum, T. konin ii, T. v~ride and T<br />

TZiTat3-5iiAlTe A i i d ~ s ~ a n ~ was o r seen ~ , on<br />

four plant pathogens i.e. Curvularia lunata,<br />

Helminthosporium or zae, Alternaria s o l a n d<br />

Rhozopus nodosus. -&- e percentage <strong>of</strong> spore germination<br />

wasdetermined and it was found that spore<br />

germination was inhibited when the spores were in<br />

contact with the volatiles from Trichoderma species.<br />

NITIN SAKSEIIA and H.H.S. Tripathi. Oepartment <strong>of</strong><br />

Botany, Univeristy <strong>of</strong> Saugar, Sagar (M.P.) 470 003,<br />

India.<br />

Antagonistic effects <strong>of</strong> volatiles <strong>of</strong> Saccharornyces<br />

against some human pathogenic fungi.<br />

Ten species <strong>of</strong> Saccharomyces (S, bis orus<br />

carlsber ensis, ra ilis, T%TFFT: -%<br />

diastitick t r k s k , S. tvrbidans, S.<br />

uvarum, S. rouxii, and S. chevalieq were screenea<br />

forlai?mainst =me five human ~athoaenic<br />

Saccharom ces and that the gas mixtures produced in<br />

d i t e d the sporulation <strong>of</strong> the pathogens to<br />

a large extent.<br />

Schlagnhaufer, B., see Wach, M. P., et. al.<br />

Schoknecht, J. D., see Keller, H. W.<br />

Schulz, R. W., see Gessner, R. V., et. al.<br />

M. A. SHERWOOD-PIKE. Geology Department, University<br />

<strong>of</strong> Oregon, Eugene, OR 97403.<br />

Taxonomy <strong>of</strong> dispersed fossil fungus spores from<br />

Clarkia, northern Idaho.<br />

A diverse assemblage <strong>of</strong> fungal spores was recovered<br />

from Miocene lakebed sediments from Clarkia, Idaho<br />

using standard palynological techniques. Approximately<br />

150 distinct taxa are present. Of those which<br />

have modern analogues, the greatest number are dematiaceous<br />

hyphomycetes. Ascospores <strong>of</strong> Xylariaceae<br />

and loculoascomycetes are also abundant. Although<br />

small spores resembling basidiospores occur, they<br />

are not common. While conditions <strong>of</strong> preservation at<br />

Clarkia are exceptionally good, thin-walled and<br />

hyaline spores have undoubtedly been selectively<br />

destroyed. The absence <strong>of</strong> Uredinales is a striking<br />

feature <strong>of</strong> this and other Tertiary assemblages.<br />

Among the most spectacular spores found are several<br />

cheiroid types and conidia essentially identical to<br />

those <strong>of</strong> the modern aquatic hyphomycete Helicoon<br />

giganteum.<br />

M. A. SHERWOOD-PIKE, Geology Department, University<br />

<strong>of</strong> Oreeon. - - Eunene. - . OR 97403.<br />

Paleoecology <strong>of</strong> a Miocene Myc<strong>of</strong>lora.<br />

Fungal spores and fruitbodies are abundant in many<br />

Tertiary fossil assemblages. A detailed census <strong>of</strong><br />

isolated spores extracted using palynological techniques<br />

and fruitbodies occurring on leaves provided


a data set for analysis and comparison with observations<br />

on the tracheophyte flora <strong>of</strong> the site. A<br />

depauperate flora <strong>of</strong> epiphyllous fungi (e.g. Microthyriaceae,<br />

Meliola) correlates with a cooling climate<br />

and predominantly deciduous flora. Species<br />

composition and relative frequencies <strong>of</strong> dispersed<br />

fungal spores underwent significant changes during<br />

the lacustrine cycle represented by the Clarkia sediments.<br />

Very large spores are more numerous in the<br />

upper, oxidized layers <strong>of</strong> the sediments, possitly<br />

because <strong>of</strong> in situ degradation as the lake became<br />

shallower. Other changes in fungal species composition<br />

may be related to local changes in the tracheophyte<br />

flora or to a changing decompositional environment<br />

due to altered moisture relations. A number <strong>of</strong><br />

highly distinctive spores found at Clarkia have not<br />

been reported elsewhere in the Tertiary; conversely.<br />

there are several spore types characteristic <strong>of</strong> early<br />

Tertiary assemblages which do not occur at Clarkia.<br />

This supports the view that there are fungal spores<br />

whose biogeographic and/or stratigraphic distribution<br />

is limited enough to render them useful tools in<br />

biostratigraphy.<br />

-- T. SEWALL and J. POMMERVILLE. The Department <strong>of</strong><br />

B~ology, Texas A&M University, College Station, TX 77843.<br />

Experimental stud~es <strong>of</strong> gamete cleavage in Allomyces<br />

macrogynus.<br />

The process by which gametes <strong>of</strong> the Chytridlomycete,<br />

Allomyces macrogynus, are formed is not clearly<br />

understood and the problem <strong>of</strong> the orlgin and assembly <strong>of</strong><br />

gamete plasma membrane has not been adequately<br />

addressed in previous studies. Because the Golgl complex<br />

has not been structurally demonstrated and endomembrane<br />

functions have not been elucidated in .4Ilomyces, we used<br />

gametangia grown in droplets <strong>of</strong> culture med~um to follow<br />

development, cleavage, and release <strong>of</strong> uninucleate<br />

planogametes. Transmission electron microscopic<br />

observations <strong>of</strong> cytoplasmic cleavage were conducted using<br />

fixations for enhancement <strong>of</strong> membrane contrast.<br />

Gametangia induced to sporulate with dllute salts (DS)<br />

containing the ionophore, monensin, took much longer to<br />

release gametes than those induced with DS only.<br />

Induction with DS containrng 50 fl monensin resulted in<br />

attenuation <strong>of</strong> cleavage membrane assembly and<br />

subsequent release <strong>of</strong> abnormal gametes with multiple<br />

flagella and nuclei. Monensin is known to affect the ion<br />

gradlent <strong>of</strong> the trans (mature) clsternae <strong>of</strong> the Golgi<br />

complex causing them to dilate and be released as swollen<br />

vacuoles. Although the structural equivalent <strong>of</strong> the Golgi<br />

complex has not been shown in Allomyces, cytochemistry<br />

has indicated its functional equivalent does exrst as<br />

scattered cr sternal or vesicular elements. It appears that<br />

Golgl complex-l~ke functions play a major role in gamete<br />

cleavage in 4. macrogynus.<br />

E.C. SETLIFF and W.C. CHUNG. Forintek Canada<br />

Corp., Western Laboratory, 6620 N.W. Marine Drive,<br />

Vancouver, B.C. V6T 1x2.<br />

The decay <strong>of</strong> Ganoderma applanatum hyphae.<br />

When basidiocarp tissue <strong>of</strong> the white-rot fungus<br />

Ganoderma applanatum (Pers : S.F. Gray) Pat. was<br />

examined from field collections, some samples were<br />

found to have turned from their original dark brown<br />

color to white. Microscopic observations showed<br />

that the bleaching phenomenon was associated with<br />

hyphal discoloration, disintegration, and<br />

disappearance. It was hypothesized that this<br />

bleaching and disintegration <strong>of</strong> fungal tissue may<br />

have been due to the same decay processes that<br />

occur in wood with advanced white-rot.<br />

This led to the question as to whether or not<br />

39<br />

wood-destroying fungi could decay fungal cell<br />

walls. In a soil block test, the wood-destroying<br />

fungi Coriolus versicolor (L. : Fr.) QuGl., Poria<br />

subvermispora PilZt and d placenta (Fr. Cke.<br />

were grown on Pomitopsis pinicola (Pr.) Karst. and<br />

- G. gplanatum fungal substrates and on Alnus rubra<br />

Bong. wood. Based on this preliminary test, it<br />

appears that these fungi are capable <strong>of</strong> causing<br />

substantial decay in fungal cell walls.<br />

Shih, L., see Muel ler, G. M., et. a1 .<br />

- N. SHISHKOFF, Dept. Plant Pathology, Cornell University,<br />

Ithaca, N.Y., 14853. Pattern <strong>of</strong> suberization <strong>of</strong><br />

the,hypodermis <strong>of</strong> onion roots and its relation to pattern<br />

<strong>of</strong> infection by root invading fungi.<br />

The hypodermis <strong>of</strong> roots is a differentiate3 layer <strong>of</strong><br />

cells beneath the epidermis. In some plant families,<br />

such as the Compositae, Liliaceae, Primulaceae, and<br />

Scrophulariaceae, among others, members have a hypodermis<br />

made up <strong>of</strong> two kinds <strong>of</strong> cells -- long rectangular<br />

ones, and short, sometimes isodiametric ones --<br />

which are arranged in a regular pattern. Endomycorrhizal<br />

fungi and certain plant pathogenic fungi usual-<br />

ly penetrate the short cells. Of 124 hypodermal penetrations<br />

on differentiated onion (~llium cepa L.)<br />

root by. Glomus albidus Walker & Rhodes, 99% occurred<br />

through short cells. Of 438 hypodermal penetrations<br />

by Pyrenochaeta terrestris Gorenz, Walker & Carson,<br />

99% were through the short cells. Toluidine blue,<br />

Sudan black B, Sudan IV, and phloroglucinol with HC1<br />

were used to identify suberin in the hypodermis - - <strong>of</strong><br />

onion, Hoya carnosa L., and Maianthemum canadense<br />

Desf. The Casparian strip develops first, in the radial<br />

walls <strong>of</strong> all hypodermal cells. Then the long<br />

rectangular cells become completely suberized. Late<br />

in development, the short cells may become completely<br />

suberized. Until then, the inner and outer tangential<br />

walls are permeable to a number <strong>of</strong> stains, including<br />

aniline blue, calc<strong>of</strong>luor white, neutral red,<br />

and alizarin red sulfate.<br />

Shortle, W. C., see Taylor, R., et. al.<br />

M. E. Silliker. Department <strong>of</strong> Botany, University <strong>of</strong><br />

California, Berkeley, CA 94720.<br />

Mitochondrial inheritance in the Myxomycete,<br />

Didymium iridis.<br />

Didymium iridis (Ditmar) Fries (Order Physarales)<br />

is an isogamous organism; presumably both parents<br />

contribute equally to the mitochondrial population<br />

in the zygote. A large coenocytic plasmodium is<br />

established, precluding cell division as a mechanism<br />

<strong>of</strong> segregating parental mitochondrial types. What<br />

is the fate <strong>of</strong> the two parent's mitochondria in<br />

the life cycle? Restriction enzyme digest pr<strong>of</strong>iles<br />

<strong>of</strong> the mitochondrial DNA were used to trace the<br />

relative survival <strong>of</strong> each mitochondrial type in<br />

crosses. The following results were obtained.<br />

(1) Haploid strains have a distinct and characteristic<br />

restriction pattern although some bands are<br />

conserved between strains. (2) Both parental mitochondrial<br />

types can be detected in plasmodia after<br />

prolonged growth although one parental type is more<br />

abundant than the other in each cross. Based on<br />

these results, I conclude that there is a high<br />

tolerance for mixed mitochondrial populations in<br />

the plasmodium although selection and/or drift<br />

occurs. Mitochondrial inheritance in Didymium will<br />

be compared to different patterns <strong>of</strong> organelle<br />

inheritance in other isogamous organisms. The


40<br />

relationship <strong>of</strong> these results to the life cycle and<br />

the phylogeny <strong>of</strong> D. iridis will be discussed.<br />

J.C. SILVER and D. PEKKALA. University <strong>of</strong> Toronto,<br />

Scarborough Campus, 1265 Military Trail, West Hill,<br />

Canada M1C 1A4. Environmentally induced alterations<br />

in chromatin and protein synthesis in Achlya.<br />

Cell stress such as heat shock, results in several<br />

changes at both the cellular and the molecular levels<br />

in both the oomycete Achlya ambisexualis and in the<br />

zygmocyte Entomophthora aulicae. In both organisms a<br />

characteristic set <strong>of</strong> "stress proteins" is induced<br />

which can be found associated with specific cytoplasmic<br />

and/or nuclear fractions. Interestingly, two <strong>of</strong><br />

the characteristic Achlya heat-shock proteins i.e.<br />

the 74kD and the 86kD proteins appear similar to two<br />

Achlya developmentally regulated nuclear proteins induced<br />

by the steroid hormone antheridiol. In Achlya<br />

heat-shock results in changes in chromatin structure<br />

and in the sensitivity <strong>of</strong> Achlya chromatin to the<br />

enzyme DNase I. The changes in chromatin structure<br />

appear related to the increased histone phosphorylation<br />

which accompanies heat-shock. Heat shock also<br />

appears to alter the deposition <strong>of</strong> actin in Achlya.<br />

For example, nuclei in heat-shocked cells contain<br />

large bundles <strong>of</strong> parallel-oriented filaments and,<br />

studies with NBD-phallocidin, an actin specific<br />

stain, indicate that these intranuclear filaments<br />

contain actin. With heat-shock, the dephosphorylation<br />

<strong>of</strong> a major group <strong>of</strong> 30kD Achlya phosphoproteins was<br />

noted. These proteins could be isolated from Achlya<br />

ribosomes and appear analogous to mammalian ribosomal<br />

protein S6. Changes in the phosphorylation <strong>of</strong> these<br />

and other ribosome-associated proteins may be involved<br />

in the changes observed in the rate <strong>of</strong> protein<br />

synthesis during heat shock.<br />

(Supported by grants from NSERC Canada to J.C.S.)<br />

Silver, J. C., see Rrunt, S. A.<br />

Silver, J. C., see Pekkala, D.<br />

Simmons, C. A., see Kerwin, J. L., et. al.<br />

Smol ich, B. D., see Taylor, J. W., et. a1 .<br />

F. W. SPIEGEL, Department <strong>of</strong> Botany and Microbiology,<br />

University <strong>of</strong> Arkansas, Fayetteville, AR 72701. The<br />

obligately amoeboid cells <strong>of</strong> Eumycetozoa - evidence<br />

for several unique evolutionary origins.<br />

Several <strong>of</strong> the flagellate protostelids and the<br />

myxomycetes have an obligately amoeboid state in the<br />

life cycle which will not become flagellate when<br />

placed in liquid. A well known example <strong>of</strong> such a<br />

state is the plasmoddiun <strong>of</strong> myxomycetes. Among the<br />

protostelids obligate amoebae may be plasmodia,<br />

plurinucleate amoebae, or uninucleate amoebae. In<br />

order to determine the phy1ogeneti.c significance <strong>of</strong><br />

this state <strong>of</strong> the life cycle, it Is necessary to<br />

determine whether it is homologous for all members<br />

<strong>of</strong> the group or if it has evolved independently<br />

several times. Evidence for common origin would only<br />

support data gathered on the flagellar apparatus and<br />

mitosis <strong>of</strong> amoebo-flagellate cells; evidence for<br />

separate origins would help to define some <strong>of</strong> the<br />

major clades <strong>of</strong> Eumycetozoa. Ultrastructure <strong>of</strong> the<br />

cytoskeleton and, in some cases, mitosis in the<br />

obligate amebae <strong>of</strong> Cavostelium apophysatum,<br />

Protosporangium articulatum, and Ceratiomyxella<br />

tahitiensis suggests that the obligately amoeboid<br />

state has evolved independently in each <strong>of</strong> these<br />

species. The characters <strong>of</strong> these states <strong>of</strong> the life<br />

cycle may now be used to identify relationships<br />

between flagellate and non-flagellate Eumvcetozoa.<br />

Supported by NSF grant BSR 83-07376<br />

L. J. SPIELMAN and M. HUBBES. Faculty <strong>of</strong> Forestry,<br />

University <strong>of</strong> Toronto, Toronto, Ont., Canada MSS 1Al.<br />

Variation in virulence and isozyme patterns <strong>of</strong><br />

Septoria musiva, agent <strong>of</strong> Septoria canker <strong>of</strong> hybrid<br />

poplar.<br />

Septoria musiva Pk. causes a serious canker disease<br />

in hybrid poplar plantations and nurseries in the<br />

United States, but is insignificant in Ontario plantations<br />

and nurseries planted with the same clones.<br />

The objective <strong>of</strong> this study was to determine whether<br />

genetic differences between the fungal populations<br />

in Ontario and the U.S. could be responsible for the<br />

low level <strong>of</strong> disease in Ontario. Isozyme patterns<br />

and virulence on hybrid poplars were compared among<br />

isolates <strong>of</strong> 5. musiva from 4 states in the U.S. and<br />

5 locations in Ontario. Patterns <strong>of</strong> acid phosphatase,<br />

alkaline phosphatase, hexokinase, peroxidase,<br />

peptidase, and other enzymes, revealed a high level<br />

<strong>of</strong> genetic variation but showed little regional<br />

differentiation among isolates. IVhen inoculated<br />

into hybrid poplar clones by placement <strong>of</strong> a mycelial<br />

plug over a small wound in the stem, some isolates<br />

varied in virulence depending on the clone, but<br />

other isolates consistently showed either high or<br />

low virulence. Isolates with high virulence originated<br />

from both the U.S. and Ontario, and there was<br />

no difference in the distribution <strong>of</strong> high and low<br />

virulence among isolates from the two countries.<br />

There was no correlation between isozyme patterns<br />

and virulence. Based on these results, we conclude<br />

that 2. musiva exhibits low regional variation in<br />

genotypes, and that populations in Ontario are genetically<br />

similar to populations in other poplargrowing<br />

regions <strong>of</strong> North <strong>America</strong>.<br />

Sriskantha, 4., see Wach, M. P., et. al.<br />

Steiner, S., see Hu, F.-S, et. al.<br />

Stempen, H., see Evans, R. C.<br />

Strickland, R., see Pommerville, J., et. al.<br />

Suryanarayana, K., see Thomas, D. des S.<br />

Sussman, D. A., see Hammill, T. M., et. al.<br />

J. B. SUTHE~ND. BioSource Institute and the Institute<br />

<strong>of</strong> Wood Research, Michigan Technological University,<br />

Houghton, MI 49931. Cellulase and B-glucosidase<br />

regulation in Ischnoderma resinosum.<br />

The white-rot fungus Ischnoderma resinosum, a member<br />

<strong>of</strong> the Poly-ooraceae, was grown with various carbohydrates<br />

in stationary liquid media. Extracellular<br />

filter paper activity, carboxymethyl cellulase, and<br />

8-glucosidase were determined by the 2,4-dinitrosalicylic<br />

acid method. Filter paper activity and carboxymethyl<br />

cellulase were higher in cultures grown on<br />

carboxymethyl cellulose than on either xylan or D-<br />

glucose. In succinate-grown cultures, the addition<br />

<strong>of</strong> either D-cellobiose or carboxymethyl cellulose resulted<br />

in the induction <strong>of</strong> carboxymethyl cellulase.<br />

Cultures grown with carboxymethyl cellulose plus a<br />

second carbohydrate were tested for catabolite repression<br />

<strong>of</strong> cellulase activity. Both filter paper<br />

activity and carboxymethyl cellulase were repressed<br />

by D-xylose, L-arabinose, L-fucose, and D-glucuronic<br />

acid. Carboxymethyl cellulase was also repressed by


D-glucose, D-galactose, L-rhamnose, D-mannose, D-cellobiose,<br />

pectin, D-galacturonic acid, and xylan. B-<br />

Glucosidase activity was induced in succinate-grown<br />

cultures <strong>of</strong> I. resinosum by D-cellobiose. Although<br />

xylan did not induce B-glucosidase in succinate-grown<br />

cultures, 6-glucosidase activity was higher in carboxymethyl<br />

cellulose-grown cultures if xylan was included.<br />

J.W. TAYLOR, B.D. SMOLICH and G. MAY. Department<br />

<strong>of</strong> Botany, University <strong>of</strong> California, Berkeley, CA<br />

94720. Mitochondria1 DNA evolution in the genus Neurospora<br />

Our study <strong>of</strong> the evolution <strong>of</strong> heterothallic Neurospora spp.<br />

by restriction endonuclease analysis <strong>of</strong> mitochondrial<br />

DNA aims to determine the occurrence <strong>of</strong> ca. 150 sites<br />

recognized by 15 endonucleases in 20 isolates <strong>of</strong> N. crassa,<br />

6 isolates <strong>of</strong> N. intermedia, 5 isolates <strong>of</strong> N. sitophila, and 4<br />

isolates <strong>of</strong> N. tetrasperma In N. crassa we find ten mitochondrial<br />

types, eight <strong>of</strong> which are very similar (separated<br />

by three or less length mutations and 1 site change). The<br />

other two types are distinct (at least 5 length mutations<br />

and 1 site change). Assuming the absence <strong>of</strong> mitochondrial<br />

recombination, the distribution <strong>of</strong> mutations indicates<br />

that length mutations can arise independently.<br />

Comparison <strong>of</strong> the N. crassa mitochondrial types with<br />

preliminary analyses <strong>of</strong> Eco RI restriction fragments <strong>of</strong> the<br />

other isolates shows that both N. sitophilaand N.<br />

tetrasperma form distinct groups but that N. crassa and N.<br />

intermedia isolates are very similar. These results are consistent<br />

with mating data that suggest a hybrid origin for N.<br />

intermedia with N. crassa as the protoperitheciating parent.<br />

Our results suggest that this approach to the study <strong>of</strong> fungal<br />

evolution will be very useful at the population and<br />

species level. Our information permits selection <strong>of</strong><br />

appropriately variable DNA fragments for studies at<br />

higher taxonomic levels.<br />

R. Ta lor, W.V. Dashek, W.C. Shortle and J.E.<br />

& Biology Department, Atlanta University,<br />

Atlanta, GA 30314 and Northeastern Forest Experiment<br />

Station, Durham, NH 03824. Polyphenol oxidase: A<br />

possible regulator <strong>of</strong> the bimodal growth response <strong>of</strong><br />

Coriolus versicolor to polyphenols in culture.<br />

Growth <strong>of</strong> C. versicolor, a wood-decay fungus, in<br />

culture is either inhibited or stimulated by catechol<br />

(CT) dependin9 uDon the ~0lv~hen01 's addition time. -.<br />

whereas' CT inhibited growthvat early log phase, it<br />

stimulated growth during either stationary or decline<br />

phases. Early CT provision (3 day) both altered mitochondrial<br />

pr<strong>of</strong>iles and reduced RER and electron-dense<br />

coated vesicle quantities but late CT supplementation<br />

(13 day) yielded hvphae with abundant electron dense<br />

granules.- To test the hypothesis that these CTinduced<br />

effects could be due to an extracellular<br />

polyphenoloxidase (PPO) yielding a growth modulating<br />

compound, we examined the time-dependent appearance<br />

<strong>of</strong> extracellular PPO emanating from C. versicolor<br />

grown upon a defined medium. ExtracXlular PPO was<br />

detected 8 days after inoculation provided that the<br />

enzyme was assayed at 30' with lOOmM CT in 100mM,<br />

pH 5.0 acetate buffer. This activity was linear<br />

with increasing enzyme concentration and was affected<br />

by boiling. Sephadex 6-100 gel filtration <strong>of</strong> medium<br />

from cultures grown in CT's absence revealed multiple<br />

peaks exhibiting PPO activity. Whereas one eluted<br />

within the void volume, others were retarded. A<br />

comparison <strong>of</strong> extracellular PPO elution pr<strong>of</strong>iles<br />

from medium for cultures grown either in CT's presence<br />

or absence will be detailed.<br />

Tewari, J. P. see Royetchko, S. M.<br />

D. des S. THOMAS and K. SURYANARAYANA, Department<br />

<strong>of</strong> Biology, University <strong>of</strong> Windsor, Windsor,<br />

Ont. Canada N9B 3P4. Calmodulin and<br />

actin during asexual sporulation <strong>of</strong> Achlya.<br />

Recently, we reported the isolation and characterization<br />

<strong>of</strong> a ca2+-dependent activator<br />

protein (Calmodulin, CM) from the water mold<br />

Achlya ambisexualis. This protein, as visualized<br />

bv Indirect Immun<strong>of</strong>luorescence is localized<br />

throughout the cytoplasm as a diffuse<br />

array <strong>of</strong> filaments. Fluorescence is particularly<br />

intense at the hyphal apex. Yhen the<br />

vegetative tip is induced to differentiate<br />

into an asexual sporangium, CM becomes concentrated<br />

in the apical papilla. A band <strong>of</strong><br />

CM persists as a collar around the exit pore<br />

after spore release. Collars <strong>of</strong> CM are also<br />

associated with exit pores <strong>of</strong> both achlyoid<br />

and dictyuchoid cysts <strong>of</strong> Achlya. This suggests<br />

that CM may be associated with sporangial<br />

and cyst lysis (secretion-related<br />

phenomena). We also localized F-actin in<br />

Achlya using rhodamine-conjugated phalloidin.<br />

Peripheral actin plaques are aggregated at<br />

the growing tip. This aggregation disappears<br />

when the tip is induced to become a sporangium.<br />

The maturing sporangia contain intranuclear<br />

actin that remains even in fresh<br />

cysts. Concentrations <strong>of</strong> actin plaques are<br />

also associated with the sites <strong>of</strong> germ tube<br />

and branch emergence. We believe that actin<br />

plaques may be a cytoskeletal link between<br />

the plasma membrane and the cell wall.<br />

T<strong>of</strong>t, D. O., see Riehl, R. M.<br />

Tripathi, H. H. S., see Saksena, Y., a.<br />

Tripathi, H. H. S., see Saksena, N., b.<br />

B. E. TUCKER. Dept. <strong>of</strong> Plant Pathology, N.Y. State<br />

Agr. Exp. Sta., Geneva NY 14456.<br />

The adhesive secondary - mores . (letiferis~ores) <strong>of</strong><br />

Macrobiotophthora vermicola, a nematophagous Entomophthorales<br />

(Zygomycetes): Factors affecting spore<br />

formation and adhesion to the host cuticle.<br />

The formation <strong>of</strong> the letiferispore, by resporulation<br />

<strong>of</strong> a forcibly discharged primary spore (conidium),<br />

is a central event in the life cycle <strong>of</strong> M. vermicola.<br />

The life cycle <strong>of</strong> this nematode destroying Entomophthorales<br />

is presented, and the ultrastructure <strong>of</strong><br />

letiferispore formation is described.<br />

The material responsible for adhesion is mucilagenous,<br />

histologically positive for protein and<br />

carbohydrate, and appears fibrillar when fixed conventionally<br />

for TEM.<br />

Various physical, chemical, and enzymatic treatments<br />

<strong>of</strong> host nematodes failed to prevent adhesion<br />

<strong>of</strong> the letiferispores. The presence <strong>of</strong> a lectinmediated<br />

host recognitionlattachment system (as<br />

found in the Deuteromycetes) is contraindicated by<br />

these results.<br />

41


B. E. TUCKER. Dept. <strong>of</strong> Plant Pathology, N.Y. State<br />

Agr. Exp. Sta.. Geneva NY 14456.<br />

The Nucleus-Associated Organelle <strong>of</strong> Macrobiotophthora<br />

vermicola, a nematophagous Entomophthorales.<br />

The morphology <strong>of</strong> the nucleus-associated organelle<br />

is an important character for current attempts to<br />

elucidate the phylogenetic relationships within the<br />

order Entomophthorales (Zygomycetes). To date, only<br />

five members have been examined, representing three<br />

families, revealing four different morphologies in<br />

NAO ultrastructure. This poster reports the ultrastructural<br />

morphology <strong>of</strong> the NAO <strong>of</strong> Macrobiotophthora<br />

vermicola, which in conventional fixation<br />

appears as a simple hollow cylinder measuring 170<br />

x 90 nm with the internal channel measuring 60 nm<br />

in diamter. The intranuclear component <strong>of</strong> the NAO<br />

consists <strong>of</strong> electron opaque material occluding the<br />

nuclear pores. Intranuclear spindle microtubules<br />

emanate directly from the NAO-INC.<br />

The NAO <strong>of</strong> 5. vermicola is morphologically most<br />

similar to those observed in Basidiobolus ranarum,<br />

and are significantly smaller and lack the fibrillar<br />

taillhandle that is found in Erynia neoaphidis and<br />

Strongwellsea magna.<br />

G.A. Tuttle and J.P. Jones. Dept. Plant Pathology<br />

and Crop Physiology, Louisiana Agricultural<br />

Experiment Station. Louisiana State University<br />

Agricultural Center, Baton Rouge. LA 70803.<br />

Cultural and cytological studies <strong>of</strong> the Hysteriales.<br />

Members <strong>of</strong> the Hysteriales (Loculoascomycetidae) have<br />

been collected from the Gulf Coast area <strong>of</strong> the U.S.,<br />

mainly southern Louisiana, for the past two years.<br />

Commonly collected orgainsms include Rhytidhysterium<br />

--<br />

rufulum. Glonium stellatum, Gloniopsis praelonga, g.<br />

curvata, Hysterographium & and Hysterium insidens.<br />

Cultural studies have been initiated to attem~t to<br />

produce the anamorphs <strong>of</strong> these organinsms. S'ingle<br />

ascospore cultures were established, when possible,<br />

on potato dextrose agar or corn meal agar amended<br />

with two percent glycerin. The anamorph <strong>of</strong> G.<br />

stellatum (Sphaeronaema byssoideum Lohman ?) could be<br />

induced to form when cultures were grown in<br />

continuous light but cultures grown in continuous<br />

darkness failed to fruit. Cytological studies have<br />

been conducted with Glonium stellatum and Gloniopsis<br />

sp. Ascus development in these organisms is similar<br />

to that reported for other ascomycetes. Crozier<br />

formation is followed by karyogamy, meiosis and<br />

mitosis, resulting in eight uninucleate ascospores.<br />

In g. stellatum one additional mitotic division<br />

occurs in the ascospore followed by septun formation,<br />

resulting in a two-celled ascospore with one nucleus<br />

per cell. In Gloniopsis sp. repeated mitotic<br />

divisions with concomitant septum formation in the<br />

ascospore results in a muriform hyaline spore.<br />

Ull rich, R. C., see Chase, T. E.<br />

B. VILGALYS, J. L- JOHNSON, and 0. K. MILLER, JR.<br />

Departments <strong>of</strong> Biology and Anaerobic Microbiology,<br />

Virginia Polytechnic Institute and State University,<br />

Blacksburg, VA 24061. Preliminary characterization <strong>of</strong><br />

DNA' s from Col lvbia species.<br />

Nucleic acid studies involving DNA homology can provide<br />

valuable information for fungal systematics. We have<br />

characterized several fungal DNA' s isolated from<br />

species <strong>of</strong> ollvbia. Collvbia drvoohil* and c.<br />

bubsul~hurea are two closely related, yet intersterile,<br />

species common in North <strong>America</strong>. Both species possess<br />

DNA with a base composition <strong>of</strong> 45% G+C, a relatively low<br />

value for Basidiomycetes. Methods for isolation <strong>of</strong><br />

whole-cell DNA will be presented. The significance <strong>of</strong><br />

DNA homology to systematics <strong>of</strong> Collvbia will be<br />

discussed.<br />

p. VILGALYS and 0. K. MILLER, JR. Dept. <strong>of</strong> Biology,<br />

Virginia Polytechnic Institute and State University,<br />

Blacksburg, VA 24061. Evolutionary systematics <strong>of</strong><br />

Collvbia ~rvoohila<br />

.<br />

The Collvbia glrvo~hila complex consfsts <strong>of</strong> at least six<br />

intersterile groups worldwide. Mating compatibility<br />

within each group is regulated by bifactorial<br />

incompatibility with multiple alleles. In addition,<br />

crosses within one group show heterogenic<br />

incompatibility between geographically separated<br />

populations. Nuclear migration is reduced or absent in<br />

all groups examined. Europe and North <strong>America</strong> each<br />

contain four intersterile groups. Within either<br />

continent, different groups can be distinguished by one<br />

to several reliable morphological features. Groups<br />

existing sympatrically thus behave as good biological<br />

and taxonomic species. Three <strong>of</strong> the European groups<br />

are each intercompatible with one <strong>of</strong> three groups from<br />

North <strong>America</strong>, suggesting conspecificity. Basidiocarps<br />

from intercompatible allopatric populations, however,<br />

are morphologically dissimillar. Electrophoretic<br />

evidence indicates that these allopatric populations<br />

are genetically divergent at a number <strong>of</strong> isozyme loci.<br />

Studies <strong>of</strong> i sozyme inheritance in laboratory<br />

synthesized dikaryons also suggest that divergent<br />

populations <strong>of</strong> the same group show differential<br />

expression <strong>of</strong> isozyme loci. Mating compatibility<br />

between allopatric populations may therefore not be a<br />

good criterion <strong>of</strong> conspecificity. A geographic<br />

component to genetic variation in the drvoohile<br />

group is consfstent with allopatric models <strong>of</strong><br />

evolution. The significance <strong>of</strong> the results to fungal<br />

systematics and evolution wi 11 be discussed.<br />

H.S. VISHNIAC. Dept. Botany and Microbiology, Oklahoma<br />

State University, Stillwater OK 74078. Ribosomal RNA<br />

homologies in the definition <strong>of</strong> basidiobl astomycete<br />

taxa.<br />

The dogma <strong>of</strong> molecular phylogeny states that base<br />

changes in rRNA occur, on average, at constant rates,<br />

so that differences numerous enough to represent an<br />

average rate are proportional to evolutionary distance<br />

The 5s rRNA sequence comparisons <strong>of</strong> Walker and Doolittle<br />

and <strong>of</strong> Huysmans and co-workers indicate an<br />

early divergence <strong>of</strong> Teliomycetes from other fungal<br />

groups, separating those heterobasidiomycetous yeasts<br />

which are doliporous (Filobasidium and a1 1 ies) from<br />

adoliporous yeasts such as Sporidi'obolus and Rhodosporidium.<br />

The larger information content <strong>of</strong>Z5SrRNA<br />

permits superior systematic resolution (to the 1 eve1<br />

<strong>of</strong> genus). Although it also inhibits sequencing,<br />

rRNA-DNA hybridization yields average base sequence<br />

homologies as precisely as required for determining<br />

relatedness. Were the dogma valid, the phylogeny <strong>of</strong><br />

basidiomycetous yeasts should be the same by either<br />

method. 255 rRNA homoloav within the aenera Filobasidiell<br />

a, Fi 1obasidium;- ~eucos~oridi;m, andTEdosporidium<br />

and within the form-genera Cryptococw<br />

Rhodotorul a. and Vanriia is conaruent with suaaested<br />

morphological definition <strong>of</strong> the;e genera, butdieither<br />

with the weight given to dolipores in this group nor<br />

with assimilation characters. Since these yeasts are<br />

more homologous with each other than with Sporidiobolus<br />

or Ustilago, the 5s rRNA phylogeny is in blatant<br />

EFEFadiction to 255 rRNA phylogeny. Ribosomal RNA<br />

homology is not an evolutionary yardstick, but a complex<br />

and conservative character useful in conjunction<br />

with other, preferably morphological, characters.


M.P. WACH, A. SRISKANTHA, K. KOONS, B. SCHLAGNHAUFER,<br />

and C.P. ROMAINE, Department <strong>of</strong> Plant Pathology, The<br />

Pennsylvania State University, University Park, PA<br />

16802. An analysis <strong>of</strong> the viruses associated with<br />

LaFrance disease <strong>of</strong> Agaricus bisporus.<br />

The name LaFrance disease is used to describe a serious<br />

malady <strong>of</strong> the cultivated mushroom, Agaricus<br />

bisporus (Lange) Imbach which is associated with several<br />

types <strong>of</strong> virus-like particles (VLPs). Sporophore<br />

isolates were analyzed for double-stranded RNA (dsRNA)<br />

by gel electrophoresis and for VLPs and a bacilliform<br />

virus by two seroassays and/or electron microscopy to<br />

further clarify the etiology <strong>of</strong> the disease. DsRNA<br />

was detected in 19 <strong>of</strong> 65 isolates and was correlated<br />

with reduced yields and, in some cases, deformed sporophores.<br />

From 2 to 12 dsRNA species xith molecular<br />

weights ranging from 4.3 to 0.21 x 10 were associated<br />

with the disease. Solid support hybridization experiments<br />

suggested that most dsRNAs represent unique<br />

nucleotide sequences. Diseased sporophore isolates<br />

also contained predominantly 19 nm and 25 nm spherical<br />

particles. The dsRNAs most frequently isolated from<br />

intact sporophores copurified with these two particles<br />

Additionally, an RNA-dependent RNA polymerase activity<br />

was detected in spherical particle-enriched preparations.<br />

Also, a single-stranded RNA bacilliform virus<br />

was encountered in ca. 70% <strong>of</strong> diseased sporophore<br />

isolates. A 280 bp copy DNA <strong>of</strong> the genomic RNA was<br />

cloned to establish a spot test for the detection <strong>of</strong><br />

the bacilliform virus and in an effort to construct a<br />

gene vector for A. bisporus.<br />

'present address : Monterey Mushrooms, Research<br />

Laboratory, P.O. Box 189, Watsonville, CA.95077.<br />

C.A. WAGNER.. Department <strong>of</strong> Botany, Ohio<br />

University, Athens, Ohio 4570i. Fine<br />

structure <strong>of</strong> the zoospores <strong>of</strong> Woronina<br />

pythii (~lasmodiophoromycetes).<br />

Free-swimming primary and secondary zoospores<br />

<strong>of</strong> ~oronina - thii , an endoparasite<br />

<strong>of</strong> Pythium (Oomycetpbere examined with<br />

electron microsco~v. The two tv~es <strong>of</strong> zoospores<br />

are ~ltrasiructurall~ inhistinqishable.<br />

Nuclei are electron-opaque with<br />

electron-translucent re~ions. Kinetosomes<br />

are 5OOnm long and occur in pairs that describe<br />

an angle ranping from 70-105 devees<br />

with respect to each other. Kinetosome<br />

cores contain clusters <strong>of</strong> dense-staining<br />

material. The kinetosomes are demarcated by<br />

a terminal plate at the distal end, proximal<br />

to the transition zone. A second plate,<br />

comparable to the axosomal plate described<br />

in many protozoans, defines the proximal end<br />

<strong>of</strong> the flagellum. Each kinetosome is associated<br />

with two simple microtubular rootlets.<br />

One consists <strong>of</strong> a pair <strong>of</strong> microtubules which<br />

appear to end at the plasmalemma a short<br />

distance from where the flagellum emerges.<br />

The second consists <strong>of</strong> three parallel microtubules<br />

which curve and follow the plasmalemma<br />

two-thirds <strong>of</strong> the way around the zoospore.<br />

The fine structure <strong>of</strong> g. pythii ZOOspores<br />

is compared with existing accounts <strong>of</strong><br />

zoospore ultrastructure in other taxa <strong>of</strong> the<br />

Plasmodiophoromycetes.<br />

43<br />

W.F. WALKER. Department <strong>of</strong> Biochemistry,<br />

Dalhousie University, Halifax, Nova Scotia,<br />

S3H 4H7. 5s ribosomal RNA sequences and<br />

ascomycete phylogenetics.<br />

A phylogenetic tree for ascomycete 5s rRHA<br />

sequences is constructed. The endomycetales<br />

yeast sequences form a diverse main branch.<br />

All sequences from mycelial ascomycetes form<br />

another main branch <strong>of</strong> about equal diversity.<br />

Sequences from Pl ectomycetes, Pyrenomycetes<br />

and Discomycetes appear to be about equidistant<br />

from each other. Sequences from<br />

Schizosaccharomyces pombi and Protomyces<br />

inundatus clearly form the most isolated<br />

sequence lineages. The P. inundatus<br />

sequence is nearly equidistant from<br />

ascomycete and ba~idiom~cete sequences.<br />

Prel imi nary results from 5.8s sequence<br />

data more clearly indicate a closer<br />

clustering <strong>of</strong> the P. inundatus sequence<br />

with basidiomycete sequences. Thus,<br />

present RNA sequence data are consistent<br />

with an origin <strong>of</strong> the basidiomycetes<br />

from an ascomycete somewhat resembl i ng<br />

Protomycetales or presumably Taphri nales.<br />

Wampler, J. E., see Lingle, W. L., et. al.<br />

Ware, C. T., see Hammill, T. M., et. al., a.<br />

Washino, R. K., see Kerwin, J. L., et. al.<br />

D. J. WEBER, E. D. BUNDERSON, and C. V. BUNDERSON<br />

Department <strong>of</strong> Botany and Range Science, Brigham Young<br />

University, Provo, UT 84602.<br />

Interactive videodisc as a tool in teaching<br />

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lnaterial for teaching mycological principles, or as a<br />

"field guide" for anyone interested in identifying<br />

fleshy fungi. The videodisc requires a videodisc<br />

player, a TV mo~itor and a n~icrocomputer. S<strong>of</strong>tware<br />

should be available for several microcmputers including<br />

the IBM-PC and the Apple Placintosh.<br />

Weber, N. S., see Cibula, W . G., et. al.<br />

A. L. WELDEN. Department <strong>of</strong> Biology and Mesoamerican<br />

Ecology Institute, Tulane University, New Orleans,<br />

LA 70118. Some distributional Patterns <strong>of</strong> the<br />

Higher Fungi <strong>of</strong> the Gulf Coast.<br />

The higher fungi <strong>of</strong> the Gulf Coast <strong>of</strong> the United<br />

States compose an unusual population <strong>of</strong> tropical,<br />

subtropical, and temperate zone species. Probably


the main reason for this mixture is the lack <strong>of</strong> any<br />

great geographical barriers separating the different<br />

zones. Six distributional patterns are exposed in<br />

this study. Three might be considered as variations<br />

on a single pattern <strong>of</strong> northward migration <strong>of</strong><br />

tropical species. A fourth pattern is the incursion<br />

<strong>of</strong> temperate species into the subtropics, the fifth<br />

is the cosmopolitan pattern; and, finally, the<br />

irrational pattern. This last pattern is undoubtedly<br />

a collection artifact, e.g., Dichopleuropus<br />

spathulatus Corner was discovered in Malaysia and<br />

is now known from its type locality and Lake George,<br />

Florida only.<br />

Imposed over these patterns are the least three<br />

factors: (1) substrate requirements, (2) critical<br />

temperature requirements for growth, and (3)<br />

altitudinal variation. For the fungi these factors<br />

are ill-understood.<br />

Approximately 25-30 Basidiomycetes, and a few<br />

Ascomycetes are shown as examples <strong>of</strong> these distribution<br />

patterns. The Basidiomycete examples are drawn<br />

mainly from thelephoroid and stereoid species, with<br />

a few polyporaceous and tremellaceous fungi added to<br />

demonstrate the wide applicability <strong>of</strong> the patterns.<br />

K. WELLS. Department <strong>of</strong> Botany, University <strong>of</strong><br />

California, Davis, CA 95616. Inter- and intracollection<br />

matings <strong>of</strong> several species <strong>of</strong> Exidiopsis<br />

(Tremellaceae).<br />

Intracollection crosses <strong>of</strong> single-spore isolates <strong>of</strong><br />

Exidiopsis plumbescens (Burt) Wells, E. diversa nom.<br />

prov., E. paniculata E. prov., E. punicea x.<br />

prov., E. calcea (Pers.) Wells, E. effusa (Bref. ex<br />

Sacc.) A. Mbller, E. grisea (Pers.) Bourd. et L.<br />

Maire, and an undesczbed species <strong>of</strong> Exodiopsis demonstrated<br />

that all species are bifactorial. In approximately<br />

50% <strong>of</strong> the mating~, hyphae with simple septa<br />

and uninucleate hyphal segments developed from the<br />

plugs taken from the contact zones (A=B= or A=Bf). In<br />

approximately 25% <strong>of</strong> the matings, hyphae with false<br />

clamps at most septa grew from the plugs. Such hyphae<br />

usually had binucleate terminal segments and uninucleate<br />

subterminal segments (A#=). In the remaining 25%<br />

<strong>of</strong> the crosses, hyphae with true clamps and binucleate<br />

hyphal segments grew from the plugs taken from the<br />

contact zones ( AfBf) . Intercollect ion matings within<br />

a species gave rise to hyphae with true clamps and<br />

binucleate hyphal segments except in those cases<br />

involving duplicate A or B factors. Plugs from the<br />

contact zones <strong>of</strong> crosses between isolates from collections<br />

<strong>of</strong> 2. plumbescens from Vancouver, B.C. south to<br />

northern California and isolates from collections east<br />

<strong>of</strong> Vancouver, B.C. and from northern Idaho usually<br />

grew out into the two monokaryons and a narrow zone<br />

between the monokaryons in which true clamp connections<br />

were formed. Clamp connections were absent in<br />

the contact zones <strong>of</strong> all interspecific crosses. The<br />

morphology <strong>of</strong> the contact zones <strong>of</strong> the interspecific<br />

crosses varied considerably.<br />

E.G. WENE and A.A. ANTBNOPO1TLOS, Argonne National Laboratory,<br />

Energy and Environmental Systems, 9700 South<br />

Cass Ave., Argonne, IL 60439. Ethanol production by<br />

Fusariwn oxyspom on D-xylose under aerobic condit<br />

ions.<br />

Xylose is a major component <strong>of</strong> monosaccharides in hydrolyzates<br />

<strong>of</strong> lignocellulose. The efficient conversion<br />

<strong>of</strong> xylose to ethanol is a major factor in determining<br />

the economic feasibility <strong>of</strong> utilizing lignocelluloses<br />

for ethanol production. Selected strains<br />

<strong>of</strong> Fusariwn oqsporwn efficiently ferment D-xylose to<br />

ethanol, with yields up to 85% <strong>of</strong> theoretical. Controlling<br />

the dissolved oxygen concentration in liquid<br />

cultures is necessary to maximize ethanol production<br />

rates and efficiency. The effect <strong>of</strong> different aeration<br />

rates and D-xylose concentrations on ethanol<br />

productivity will be discussed,<br />

Wene, E. G., see Antonopoulos, A. A.<br />

Wheeler, K. A., see Pitt, J. I., et. al.<br />

K. 0. WHITNEY and H. J. ARNOTT. Department <strong>of</strong><br />

Biology, University <strong>of</strong> Texas at Arlington, Arlington,<br />

TX 76019. Calcium oxal ate crystal devel oprnent in<br />

hyphae <strong>of</strong> Agaricus bi sporus.<br />

Aerial hyphae <strong>of</strong> Agaricus bis orus grown in agar<br />

culture produce abundant ca ?- cium oxalate crystals.<br />

These deposits, when first formed, consist <strong>of</strong><br />

elongate, acicular, "raphide-1 ike" crystals that<br />

ensheath the hypha, giving the elements <strong>of</strong> the aerial<br />

mycelium a bottle-brush appearance. SEM examination<br />

<strong>of</strong> the crystal-bearing hyphae reveals that the<br />

crystals are arranged tangenti a1 1 y on the hyphal<br />

surface. The crystals appear to originate within the<br />

wall <strong>of</strong> the hyphae and increase in length as<br />

additional calcium oxalate is added to the crystal<br />

within the hyphal wall. Scanning electron micrographs<br />

and energy-di spersive x-ray elemental analysis <strong>of</strong><br />

these crystal s will be presented.<br />

ANlTMA WILFRED, L. FREDERICK, and W. LENA AUSTIN.<br />

Hmd University, Washington, DC 20059 Nuclear<br />

behavior during ascospomgenesis in a natural mutaht<br />

<strong>of</strong> Neuxvspra dodgei, a hmthallic species.<br />

A mutant strain <strong>of</strong> NeuroSpora dodgei that appem in<br />

two corn ma1 amr culture plates is characterized by<br />

the formtion <strong>of</strong> round, oval, or peanut pod-shw<br />

ascospores that vary in nmber from 8 to 16 per ascus.<br />

Asci in which spores <strong>of</strong> the mtant form are greatly<br />

enlarged and are, in sm instances, branched. The<br />

nuclear events that occur during the formation <strong>of</strong><br />

asci <strong>of</strong> the mtant have been studied with light<br />

microscopy and canpared with those that occur in cultures<br />

<strong>of</strong> the wild type. Single ascospow isolates<br />

<strong>of</strong> the rmtant were used in the study. Nuclear events<br />

follow the sam pattern in isolates <strong>of</strong> the mutant and<br />

<strong>of</strong> the wild type through the first mitotic division.<br />

In the ascus <strong>of</strong> the wild type, after the first mitot-<br />

ic division, ascospores are delimited. In isolates<br />

<strong>of</strong> the mtant a second mitotic division usually takes<br />

place in the ascus prior to the delimitation <strong>of</strong> ascospores<br />

and results in a 16-nucleated ascal stage.<br />

Subsequently ascospore delimit at ion occurs and results<br />

in the developrrent <strong>of</strong> 8 binucleate peanut podshaped<br />

ascuspom, 16 round uninucleate ascospores ,<br />

or a mixture <strong>of</strong> from 9 to 15 round, oval, or peanut<br />

pod-shaped uninucleate or binucleate ascospo~s.<br />

Following delimitation round or oval ascuspores be-<br />

cane binucleate.<br />

not noted to be-<br />

Peanut pod-shaped ascospores were<br />

quadrinucleate after delimitation.<br />

Wilks, R. L., see Ross, I. K., et. al.<br />

GEORGE J. WONG. Department <strong>of</strong> Botany, 3190 Maile<br />

Way, University <strong>of</strong> Hawaii, Honolulu, Hawaii 96822.<br />

Interfertility between Auricularia polytricha and<br />

Auricularia t enuis.<br />

Three collections <strong>of</strong> Auricularia were collected


from Hawaii. Based on the morphology <strong>of</strong> the<br />

basidiocarps in transverse section, it was<br />

determined that two <strong>of</strong> the collections were<br />

referable to Auricularia polytricha and the third<br />

to A. tenuis. Single spores were isolated from<br />

each collection and self-crossed. Both species<br />

were found to be bifactorial, producing true clamps<br />

in AZB# crosses and false clamps in A#B= crosses.<br />

However, the bifactorial system in the two<br />

Auricularia species differs from the one observed<br />

in agarics such as Schizophyllum commune and<br />

Coprinus lagopus in that nuclear migration,<br />

apparently, does not occur and AZB= crosses are<br />

stable. Crosses performed between A. polytricha<br />

and A. tenuis produced dikaryons and fruiting <strong>of</strong><br />

selected hybrid dikaryons produced basidiocarps<br />

that are morphologically referable to<br />

A. polytricha. These preliminary results indicate<br />

-<br />

that A. polytricha and A. tenuis may be synonymous.<br />

I. E. YATES~, R. J. COLE^, J. L. UNIER~ AND J. W.<br />

DORNER~. l~oxicol. & Biol. Constit. Res. Unit,<br />

Russell Research Cen., USDAIARS, Athens, GA 30613,<br />

*National Peanut Res. Lab., USDA/ARS, Dawson, GA<br />

31742. Bacterial luminescent bioassays <strong>of</strong> aflatoxin<br />

B1 and cyclopiazonic acid toxicities.<br />

Aflatoxin B1 (AFBl), a mycotoxin whose toxicity, hepatocarcinogenicity<br />

and mutagenicity are well characterized,<br />

is produced by only a few strains <strong>of</strong> Aspergillus<br />

flavus and A. parasiticus. A. flavus can also<br />

produce cyclopiazonic acid (CPA), a mycotoxin whose<br />

acute toxicity in laboratory animals though not as<br />

severe as AFBl does cause deleterious effects. Since<br />

both toxins can be produced by A. flavus, CPA and AFBl<br />

could occur simultaneously in the food supply and<br />

interact to alter the toxic expression <strong>of</strong> one another.<br />

The effect <strong>of</strong> AFBl and other mutagens known to attack<br />

the guanine sites in DNA <strong>of</strong> a dark mutant <strong>of</strong> Photobac-<br />

45<br />

terium ~hos~horeum was to cause a reversion to the<br />

bioluminescent condition after 10 h treatment. CPA<br />

did not generate such a response but at higher doses<br />

inhibited the low level bioluminescence observed in<br />

the control by 20 h incubation. The mutant was<br />

treated with stimulatory doses <strong>of</strong> AFBl and simultaneously<br />

with CPA at low concentrations which had no<br />

effect on bioluminescence or at high concentrations<br />

which inhibited bioluminescence. Low doses <strong>of</strong> CPA had<br />

no effect on the stimulation <strong>of</strong> biolumineecence by<br />

AFBl but high doses decreased the stimulation. These<br />

results imply that in this bioassay system, high<br />

levels <strong>of</strong> CPA depress the effect <strong>of</strong> AFB1. The combined<br />

activity <strong>of</strong> the two mycotoxins were examined in<br />

a bacterial bioluminescent system designed to measure<br />

cytotoxicity.<br />

S. E. Gochenaur, Biology Department, Adelphi University,<br />

Garden City, Long Island, New York 11530.<br />

Comparative carbon nutrition <strong>of</strong> members <strong>of</strong> the<br />

EupeniciZ Zim javanica, E. Zapidosa, and E. pine tom<br />

Sections in relation to their taxonomy and ecology.<br />

A EupeniciZZiwn species isolated from an oak-birch<br />

forest is believed to be a member <strong>of</strong> the E. Zapidosa<br />

Section. It has several distinctive features that<br />

include osmophilic growth, a genetically unstable<br />

holomorph, an inability to utilize di- and polysaccharides,<br />

and an extremely slow development with<br />

colony diameters <strong>of</strong> less than 7 mm after 14 da<br />

incubation at room temperature. In spite <strong>of</strong> these<br />

features, this organism is the most abundant<br />

cleistothecial ascomycete and one <strong>of</strong> only five broad<br />

amplitude species in the A horizon. A comparison <strong>of</strong><br />

its carbon nutrition on 35 compounds to the nutrition<br />

<strong>of</strong> 18 other Eupenicillia will be presented along with<br />

some thoughts on the relationship <strong>of</strong> nutrition to the<br />

taxonomy and ecology <strong>of</strong> these species.<br />

THE UNIVERSITY OF ALBERTA MICROFUNGUS COLLECTION AND HERBARIUM<br />

Established in 1960, the University <strong>of</strong> Alberta Yicr<strong>of</strong>ungus Collection and Herbarium (UAMH)<br />

is now the second largest collection <strong>of</strong> filamentous fungi in Canada, and has become nationally<br />

and internationally recognized as an important reference and research facility. Recognizing the<br />

significance <strong>of</strong> UAMH to scientists in Canada and elsewhere, the University <strong>of</strong> Alberta, on<br />

January 1, <strong>1985</strong>, made a major commitment to the future <strong>of</strong> the collection by transferring it to<br />

the University's Devonian Botanic Garden, a facility with which it shares a common role in the<br />

preservation <strong>of</strong> living organisms. The Devonian Botanic Garden, one <strong>of</strong> six interdisciplinary<br />

units within the Office <strong>of</strong> the Vice-President (Research), is directed by P. N. D. Seymour. This<br />

amalgamation consolidates mycological expertise and facilities currently available at each <strong>of</strong><br />

the two centres and will improve the collection's eligibility for obtaining funding from<br />

non-medical granting agencies.<br />

The UAMH preserves a large and unique collection <strong>of</strong> medically important fungi as well as<br />

fungi <strong>of</strong> importance to agriculture, forestry and industry. With an increasing emphasis in<br />

Canada on development <strong>of</strong> industrial and applied research (9iotechnology), there will be an<br />

increasing requirement for accurately identified and properly maintained fungal genotypes. The<br />

objectives <strong>of</strong> the UAMH are to meet this requirement, to maintain the liason with the biological<br />

and medical communities, and to provide improved services to agriculture, forestry and<br />

industrial research.<br />

Fungi in the collection include all groups, but particular emphasis has been placed on mold<br />

fungi (Hyphomycetes). Current acces'sions number over 5000, the majority being represented by<br />

living cultures and herbarium specimens. Many cultures are derived from type collections, and<br />

are useful for verification <strong>of</strong> identifications.<br />

Completion in <strong>1985</strong> <strong>of</strong> an on-line data base containing UAMH strain records, will facilitate<br />

data distr.ibution and retrieval. This data retrieval system, when fully implemented and made<br />

public, will be accessible for on-line searches by any researcher in North <strong>America</strong>, and will<br />

facilitate selection <strong>of</strong> strains appropriate to particular research applications. Publication <strong>of</strong><br />

a new edition <strong>of</strong> the UAMH catalogue is planned for <strong>1985</strong>.<br />

Enquiries regarding UAMH services and cultures should be directed to the Curator, Lynne<br />

Sigler, University <strong>of</strong> Alberta Micr<strong>of</strong>ungus Collection and Herbarium, Devonian Botanic Garden,<br />

1-31 Med. Sci. Bldg., Edmonton, Alberta, Canada T6G 2H7.


4 6<br />

COMPUTER SOFTWARE AVAILABLE--FOR GIVE-AWAY,<br />

SALE, OR EXCHANGE<br />

Gary W. Moorman has an illustrated key to diseases <strong>of</strong> dogwood (Cornus florida) for<br />

Macintosh computer users who have Telos "Filevision" s<strong>of</strong>tware.<br />

Fred Rhoades <strong>of</strong>fers PC-TAXONIASKATAXA. It generates synoptic keys and provides rapid<br />

microcomputer access and editing, including hard-copy key printing. Define keys to 128 taxa,<br />

using 400 character-states. Requirements: IBM PCIXTIAT with 192k memory (128k for ASKATAXA<br />

which does not have editing routines), DOS 2.0 or higher, monitor capable <strong>of</strong> displaying 80<br />

column text. Specify version for IBM color adapter (card) or other adapter (non-colorcompatible<br />

cards and monochrome). $50 for full version. $5 for shortened demo version.<br />

Walter J. Sundberg has available a MYCOLOGICAL DICTIONARY DISK for use with Sensible<br />

Speller (Apple, IIe DOS 3.3), includes most terms in Snell and Dick's "A Glossary <strong>of</strong> Mycology"<br />

and more. $20.00/copy, disk included (available as <strong>of</strong> July 1).<br />

Edmund E. Tylutki would 1 ike to correspond with anyone interested in developing an expert<br />

system for Agaricales, including the application <strong>of</strong> the interactive video disk technology in<br />

the system.<br />

Rod Tul loss has two programs avai 1 able: 1) TAXON wi 11 , given specific or subspeci f i c<br />

epithet or a syllable from such an epithet, find all occurrences <strong>of</strong> that epithet (masculine,<br />

feminine, or neuter endings; capitalized or not) in a dataset. This has been implemented to<br />

search for previous applications <strong>of</strong> epithets. The program wi 11 a1 so provide i nformation on<br />

type locality (where known to the constructor <strong>of</strong> the data files). The program is implemented<br />

in UNIX (Trademark <strong>of</strong> Bell Laboratories) shell on an IBM PC XT running PCIIX. I will charge a<br />

nominal amount per floppy disk copy depending upon whether or not the inquirer supplies hislher<br />

own floppies, and 2) AMANITA.EXPERT is implemented in Univ. <strong>of</strong> New South Wales PROLOG under<br />

UNIX and makes use <strong>of</strong> the UNIX shell in part. If you're interesting in a listing, a copy on<br />

tape, or more detail about the implementation, make inquiry. The project was developed by me<br />

whi le teaching mysel f PROLOG in my job at AT&T Technologies, Engineering Research Center,<br />

Princeton, NJ. A formal release from AT&T may be necessary before the material can be shared<br />

in full.<br />

MSA PLACEMENT SERVICE<br />

The <strong>Society</strong>'s placement service has been established and is<br />

operating well to the extent that it has been used. Only ten<br />

people have placed material on file for seven positions that have<br />

been listed with the service. Prospective employers have been<br />

provided with the records <strong>of</strong> appropriate candidates. In some<br />

cases we have not been able to recommend suitable candidates for<br />

the position listed. Persons seeking placement have been sent job<br />

descriptions that fit their qualifications.<br />

For Dur placement service to be effective, we need many more<br />

records on file. There must be more than ten people who are<br />

looking for jobs at the present time! All members <strong>of</strong> the MSA need<br />

to assist in getting potential employers to list positions with<br />

our service. With more positions and candidates listed, the<br />

service should be valuable to all concerned.


EMPLOYER DATA FORM<br />

MYCOLOGICAL SOCIETY OF mRICA PLACEMENT SERVICE<br />

Please type or print all entries clearly.<br />

1. Record Number: (leave blank)<br />

2. Organization Name:<br />

3. Position Title:<br />

4. Interests. Circle letters from the following:<br />

A. Morphology B. Taxonomy C. Physiology<br />

D. Cytology E. Biochemistry F. Cell Biology<br />

G. Genetics H. Ecology I. Molecular Biology<br />

J. Pathology K. Mycorrhizae L. Medical<br />

M. Development<br />

N,O = other<br />

5. Fungal Group. Circle one or more letters from list:<br />

A. Mycetozoa B. Zoosporic Fungi C. Zygomycetes<br />

D. Ascomycetes E. Basidiomycetes F. Deuteromycetes<br />

G. Trichomycetes H. Pathogenic Fungi I. General<br />

J,K,L,M,N,O = other<br />

6. Degree or Training Desired:<br />

7. Skills Desired. Circle one or more from list:<br />

A. Teaching B. Research C. Administration<br />

D. Public Service E. Curatorial<br />

E-K = other. Please specify.<br />

Terms<br />

9. Closing Date:<br />

10. Contact Person:<br />

Appointment:<br />

11. Dept. or Organization:<br />

12. University or Company :<br />

13. Street:<br />

14. City: State Province :<br />

16. Zip or Postal: 17. Country:<br />

17. Telephone Contact:<br />

Return to: Dr. M. S. Fuller. MSA Placement. Dept. <strong>of</strong> Botany.<br />

University <strong>of</strong> Georgia. Athens, GA 30602.


EMPLOYEE DATA FORM<br />

MYCOLOGICAL SOCIETY OF AMERICA PLACEMENT SERVICE<br />

Please type or print all entries clearly.<br />

, 1. Record Number : (leave blank)<br />

2. Name: last<br />

first<br />

initial<br />

3. Department or Organization: - -<br />

4. University or Street: -----<br />

5. City:<br />

6. State or Province (abbrev.) : -<br />

7. Zip or Postal Code: -<br />

8. Country (abbrev. if >10 characters): -<br />

9. Phone Number:<br />

10. .Degree 1 (M.S. or B.s./B.A.) , Year, Pr<strong>of</strong>essor, Institution:<br />

11. Degree 2 (Ph.D.), Year, Pr<strong>of</strong>essor, Institution:<br />

12. Postdoctoral experience. Year, Pr<strong>of</strong>essor, Institution:<br />

13. Interests. Circle letters from the following:<br />

A. Morphology B. Taxonomy C. Physiology<br />

D. Cytology E. Biochemistry F. Cell Biology<br />

G. Genetics H. Ecology I. Molecular Biology<br />

J. Pathology K. Mycorrhizae L. Medical<br />

M. Development<br />

N,O = other<br />

14. Organisms <strong>of</strong> interest. Circle one or more letters from list:<br />

. .<br />

A. Mycetozoa B. Zoospor ic Fungi C. ~ygomycetes<br />

D. Ascomycetes E. Basidiomycetes F. Deuteromycetes<br />

G. Trichomycetes H. Pathogenic Fungi I. General


15. Job preference. Circle one or more letters from list:<br />

A. Industry B. Univ. teaching C. Univ. research<br />

D. Both B and C E. Governnent F. Curatorial<br />

G. Other than above<br />

Order <strong>of</strong> preference in above by letter: ---- -<br />

16-22. Narrative about job applicant. Use this space to write<br />

anything you would like to have submitted with our report to<br />

a potential employer. Write in the third person. This is<br />

the only place where you can enter special experience. You<br />

have seven lines, each with 65 characters including spaces<br />

and punctuation. You nay hyphenate at the end <strong>of</strong> a line if<br />

it saves you space. Count the number <strong>of</strong> characters per line<br />

or print on graph paper in a rectangle 7 squares by 65<br />

squares. The print out will read as text if you follow<br />

these directions. Program will not underline.<br />

Send completed form to:<br />

Dr. Melvin S. Fuller<br />

MSA Placement Service<br />

Department <strong>of</strong> Botany<br />

University <strong>of</strong> Georgia<br />

Athens, GA, 30602 USA


5 0<br />

TRAVELS AND VISITS<br />

JEAN R. BOISE joined the 8ri ti sh Yycological <strong>Society</strong> in their annual Upland Foray, this year at<br />

Bettyhill, Sutherland on the northern shore <strong>of</strong> Scotland. Then, back at Kew she visited<br />

the Royal Botanic Gardens and Commonwealth rlycol ogical Institute.<br />

Teresita I. Iturriaga lists the following visitors to her lab in 1984:<br />

February, ROY HALLING in February, and GARY SAMUELS in April.<br />

AMY ROSSMAN in<br />

ALVIN L. ROGERS is on sabbatical leave (3120-8120185) working in the laboratory <strong>of</strong> G. T. Cole<br />

on immunology <strong>of</strong> the cell wall <strong>of</strong> Candida albicans (with G. T. Cole) and on<br />

gastrointestinal and systemic candidosis in the infant mouse (with G. T. Cole and Pope).<br />

DAN ROYCE and LEE SCHISLER from Penn State were guests <strong>of</strong> Orson K. Miller, Rytas Vilgalys, and<br />

Tim Flynn and addressed the conference on cultivating Shiitake held on May 4th at the<br />

Donaldson Brown Conference Center at Vi rginia Polytechnic Institute & State University.<br />

A. L. J. COLE, Department <strong>of</strong> Botany, University <strong>of</strong> Canterbury, Christchurch, New Zealand,<br />

visited with Gareth Morgan-Jones at Auburn University, April 4-9 and presented a seminar<br />

entitled "Mycology and plant pathology in the Antipodes."<br />

FLORENCE H. NISHIDA participated in Fall 1984 Project Flora Amazonica. She collected fungi in<br />

Acu, Brasil , and will be returning to Brazil in August-September <strong>1985</strong> to visit herbaria,<br />

collect fungi in the Alantic forest and Northeast.<br />

TOMIAR TOKITA, Aseptic Cultivation Research Center <strong>of</strong> Japan, stopped by for two days to acquire<br />

a list <strong>of</strong> live cultures to take back to Japan.<br />

JAMES M. TRAPPE and SHANNON BERCH visited Y. G. Mukerji <strong>of</strong> Delhi University, India, March 29.<br />

Trappe visited David Pegler, Derek Reid, and Bryan Spooner, Royal Botanic Gardens, Yew, on<br />

March 23; and Tom Alexander, University <strong>of</strong> Marburg, Germany, March 30-April 1.<br />

ALFRED0 YUNOZ has extended his postdoctoral study at the University <strong>of</strong> Vermont.<br />

MIKE IVORY from University <strong>of</strong> Oxford visited Mike Wingfield during November to survey pine<br />

diseases, particularly needle diseases.<br />

DAVE JENKENS presented a seminar on the genus Amanita to the Botany Faculty <strong>of</strong> Virginia<br />

Polytechnic Institute and State University, Spring Quarter, <strong>1985</strong>.<br />

Visitors to INIREB in 1984 were A. L. WELDEN in July; and H. C. EVANS from the Commonwealth<br />

Mycologic Institute at Kew in November. Biologist DANIEL MARTINEZ from IVIREB visited the<br />

lab <strong>of</strong> S.-T. Chang in Hong Kong in August 1984.<br />

SCOTT REDHEAD attended the second International Symposi urn on Arctic and A1 pine Mycology at<br />

Ftan, Switzerland and the Symposium on the Tricholomataceae held in Borgotaro, Italy last<br />

fa1 1 . Papers were presented on arctic-a1 pine basidiol ichens and on Crinipell is in Canada.<br />

Visitors to the Mycology Laboratory, USDA-ARS, National Fungus Coll ections, Be1 tsvil le, MD,<br />

during the 1 ast six months included: Rot4 PETERSEN, University <strong>of</strong> Tennessee; CHARLES<br />

HODGES, USDA-FS, temporarily in Washington, DC; MARIA MARGANTA LEON, Bogota, Colombia;<br />

UDORU IJNAHAWUTHI, Bangkok, Thailand; and BEATRICE ANYANGO, Nairobi, Kenya.<br />

To learn current freeze substitution and associated techniques for electron microscopy, JANELLE<br />

CURLIN and WALTER J. SUNDBERG worked with Kerry O'Donnell and David McLaughlin at the<br />

University <strong>of</strong> Minnesota for two weeks in March.<br />

ROYALL T.<br />

MOORE spent an Autumn term (1984) in Gerlind Eger-Hummel's Laboratory in Marburg.


MELVIN S. FULLER spent May and June working with Dr. Kenneth Sederhall at the Institute <strong>of</strong><br />

Physiological Botany in Uppsal a, Sweden.<br />

Visitors to the Farlow Reference Library were: ZUEI-CHIVG CHEN, National University, Taipei;<br />

CHRISTINE YANVILLE, Academy <strong>of</strong> Natural Sciences, Philadelphia; YICHAEL VINCENT, Miami<br />

IJni versi ty, Ohio; and SHIMON TZAHAS, London.<br />

GERARD C. ADAMS travel led to Ki bale Rainforest Preserve near Fort Portal, Uganda, to diagnose<br />

the cause <strong>of</strong> high tree mortality.<br />

YICHAEL F. DOYLE visited the following areas and institutions in Hawaii during late Maylearly<br />

June, <strong>1985</strong>: Hawaii Volcano National Park, The Sishop Yuseum (Honolulu), George Wong's<br />

laboratory at the University <strong>of</strong> Hawai i at ~anoa, and the Pacific Tropical Botanical Garden<br />

(Kawai ).<br />

ASSISTANTSHIPS AND FELLOWSHIPS AVAILABLE<br />

University <strong>of</strong> Texas: Research Assistantships in mycology. Contact Dr. G. T. Cole, Department<br />

<strong>of</strong> Botany, University <strong>of</strong> Texas at Austin, Austin, TX 78712.<br />

Kansas State University: Assistantship for Y.S. or Ph.D. students to work on population<br />

genetics <strong>of</strong> Fusarium monil iforme from corn and sorghum in Kansas. Contact Dr. John F.<br />

Leslie, Dept. <strong>of</strong> Plant Pathology, Kansas State University, Throckmorton Hall, Manhattan,<br />

YS 66506. Phone: (913) 532-6176.<br />

Uni versi ty <strong>of</strong> Vermont: Teaching and/or Research Fell owshi ps, stipend ca. $6,000112 mo.,<br />

tuition remission. Contact Dr. Robert C. Ullrich, Dept. <strong>of</strong> Botany, Life Science Building,<br />

Univ. <strong>of</strong> Vermont, Burlington, VT 05405. Phone: (802) 656-2930.<br />

Brigham Young University: Teaching Assistantships. Contact Darrell Weber, Department <strong>of</strong><br />

Botany, Rri gham Young University, Provo, IJT 84602. Phone: (801) 378-2237.<br />

National University <strong>of</strong> Singapore: Research Schol arshi ps for outstanding university graduates<br />

for research leading to a master's or doctoral degree in various disciplines at the<br />

University. Scholarships are tenable for one year in the first year and, subject to<br />

sati sfactory progress, renewable annual ly for another two years. The Schol arshi ps carry<br />

monthly emoluments ranging from S$800 to $1,100 (US$1.00 = S82.13 approximately); actual<br />

emolument is determined on the candidate's qualifications and experience. Applications<br />

are invited twice a year, in August and February and dead1 ines are October 31 and April 30<br />

respecti vely. Appl ication forms may be obtained from: The Registrar, National Yni versi ty<br />

<strong>of</strong> Singapore, Kent Ridge, Singapore 0511, Republic <strong>of</strong> Singapore, and they should be sent<br />

to Dr. G. Lim, Botany Department, National University <strong>of</strong> Singapore, Kent Ridge, Singapore<br />

0511, Republ ic <strong>of</strong> Singapore.<br />

Southern Ill inoi s University: Doctoral Fellowship, for 1986-1987, with $8,500 stipend plus<br />

tuition waiver for each <strong>of</strong> 3 years (Universi ty-wide competi tion, 5 available). A1 so<br />

Teaching 4ssi stantship (avail able on Departmental competitive basis) for Y.A. or Ph.0.<br />

aspirant in SYSTEMATIC MYCOLOGY. Duties <strong>of</strong> Gen. Biology, Gen. Botany andlor Forest<br />

Pathology. Write W. J. Sundberg, Dept. <strong>of</strong> Botany, SIU, Carbondale, IL 62901.<br />

University <strong>of</strong> A1 aska: Assistantships avail able in FUNGAL PHSIOLOGY, DISEASE ASSESSMENT, etc.<br />

Contact Dr. Jenifer Huang YcBeath, Agricultural & Forestry Experiment Station, University<br />

<strong>of</strong> Alaska, Fairbanks, AK 99701.


VACANCIES FOR MYCOLOGISTS<br />

The Northern Regional Research Center (USDA) seeks the following:<br />

1. An individual with a Ph.D. degree and research experience in insect-microbe<br />

interactions for a RESEARCH SCIENTIST (Insect-Microbial Ecologist) position (GS-11/12 [$25,489<br />

to $39,7111). The individual wi 11 be responsible for conducting research involving the<br />

interactions <strong>of</strong> insects and toxigenic fungi in cereal agrocosystems. The research will examine<br />

the role <strong>of</strong> seed-infesting fungi and their secondary metabolites as these influence insect<br />

behavior and population dynamics. Specific emphasis will be given to mechanisms <strong>of</strong> insect<br />

resistance to fungal toxins. Knowedge <strong>of</strong> and experience in insect chemical ecology, insect<br />

digestive physiol ogylgut microbiology, or natural products chemistry will be factors in<br />

selecting the successful candidate. Send resume to: D. T. Wicklow, Insect/Microbi a1 Ecologist<br />

Search Committee, Northern Regional Research Center, 1815 North University Street, Peoria, IL<br />

61604.<br />

2. An individual with a Ph.D. degree and research experience in correlative ~nicroscopic<br />

and hi stochemi cal studies <strong>of</strong> the fungal infection process, for a POSTDOCTORAL SCIENTIST (Plant<br />

Pathologist) position not to exceed 4 years, in the Vycotoxins in Agricultural Systems Research<br />

group, Fermentation Laboratory (GS 11/12 [$25,489 to $39,7111). The individual will be<br />

responsible for conducting research involving the process <strong>of</strong> fungal infection and role <strong>of</strong><br />

extracell ular fungal enzymes and pathotoxins in the hi stopathol ogy <strong>of</strong> common ear and kernel<br />

rotting molds. Knowledge <strong>of</strong> and experience in transmission electron microscopy, cytochemistry,<br />

and the biochemical basis <strong>of</strong> host-parasi te interactions wi 11 be factors selecting the<br />

successful candidate. Send resume to: 0. T. Wick1 ow, Northern Regional Research Center, 1815<br />

N. University Street, Peoria, IL 61604.<br />

3. SIOLOGICAL TECHNICIAN (Fungal Ecol ogy/Pl ant Path01 ogy) for a position in the<br />

Mycotoxins in Agricultural Systems Research Group (GS 517 [$14,390 to $17,8243). Send brief<br />

resume to D. T. Wicklow, Northern Regional Research Center, 1815 North University Street,<br />

Peoria, IL 61604, and submit both a Personal Qualification Statement (U.S. Govt. Form SF-171)<br />

and a copy <strong>of</strong> college transcripts to Office <strong>of</strong> Personnel Yanagement, Chicago Area Office, Rm.<br />

1402, 55 E. Jackson, Chicago, IL 60604.<br />

Monterey Mushrooms, Inc. is seeking to fill an ENTRY-LEVEL PH.D. POSITION with the<br />

incumbent expected to work as part <strong>of</strong> an interdisciplinary research team on new and innovative<br />

projects related to yield and qual ity. They are looking for individuals who are strongly<br />

motivated, innovative and have leadership capabi 1 i ty coupled with the ability to work with<br />

others.<br />

Monterey Yushrooms, Inc. (an Amfac Company) is a national firm based in Santa Cruz,<br />

California, special izing in production and sale <strong>of</strong> high qual ity, edible mushrooms (Agaricus<br />

- bi sporus). A new 5,500 square foot research faci 1 ity was completed near Watsonvill e,<br />

California in March <strong>of</strong> <strong>1985</strong>.<br />

The successful candidate must demonstrate the ability to investigate aspects <strong>of</strong><br />

physiological , genetic, or path01 ogical problems in fungal systems, with an organismal<br />

orientation. This scientist will be responsible for research in the areas <strong>of</strong> mushroom growth,<br />

reproduction, and qual i ty. Know1 edge <strong>of</strong> nutritional supplements and composti ng science is<br />

he1 pul .<br />

The company <strong>of</strong>fers growth potential, competitive salaries and a full benefit package<br />

including re1 ocati on expense reimbursement. Send your resume or curricul um vitae with three<br />

references to: Dr. Perry Yulleavy, Monterey Mushrooms, Inc., Mushroom Research Laboratory,<br />

P.O. Box 189, Watsonville, CA 95077.<br />

SOYBEAN PLANT PATHOLOGIST (Yycol ogist)--i n connection with the Zambia Agricultural<br />

Research and Extension (ZAMARE) project. Non-tenure track position at the Assistant Pr<strong>of</strong>essor<br />

rank with the University <strong>of</strong> Illinois, dealing with fungal diseases <strong>of</strong> soybean and other field<br />

crops near Lusaka, capital <strong>of</strong> Zambia. For information, contact J. B. Sinclair, Dept. <strong>of</strong> Plant<br />

Pathology, University <strong>of</strong> Illinois, 1102 South Goodwin, Urbana, IL 61801.


POSITIONS WANTED<br />

PETER R. SECKJORU i s seeking employment in forestrylmycorrhi zal research (see Changes <strong>of</strong><br />

Address).<br />

JEYSON DANIEL is interested in a position in a Vycology or Plant Pathology lab. Ph.D. Mycology<br />

(Agaricales) , Y.Sc. (Ag.) in Plant Pathology. Experienced in Plant Pathology and Mycology<br />

lab methods (see Changes <strong>of</strong> Address).<br />

R. K. S. YUSHWAHA is searching for a post-doctoral research fellowshi? for 10-12 months. Y.S.<br />

and Ph.0. with S. C. Agrawal ; taxo-ecology <strong>of</strong> keratinophil ic and copropilous fungi.<br />

FRED RHOADES i s seeki ng a position in Yycol ogylGenera1 Biol ogylSotany undergraduate teachi ng.<br />

4vailable Fall, <strong>1985</strong>. Ph.D., 1978, llniversity <strong>of</strong> Oregon, under George Carroll.<br />

Considerable teaching experience for the 1 ast eight years. Research interests: population<br />

biology <strong>of</strong> 1 ichens and 1 i tter-decomposing basidiornycetes.<br />

BRY3EN JONES seeks a position in Forest Insect Pathology. He will receive his M.Sc. in January<br />

1986 under W. S. Kendrick and his research interests are fungi and biocontrol. His<br />

address is the nepartment <strong>of</strong> Biology, University <strong>of</strong> Waterloo, Water1 00, Ontario, Canada,<br />

N2L 3G1.<br />

GEORGE P. CHAMURIS seeks a research andlor academic post in Mycology. Ph.D. <strong>1985</strong>. With a<br />

speci a1 t y in Wood-decay Basidiornycetes; he has broad biological training and faculty<br />

training.<br />

SHOW THE GROWTH OF<br />

MUSHROOMS<br />

IN YOUR CLASSROOM<br />

Our Mushroom MiniFarms arrive mature and ready to produce their first <strong>of</strong> several crops <strong>of</strong> edible mushrooms.<br />

Reliable and guaranteed, each MiniFarm comes complete with simple instructions.<br />

These "kits" provide a fascinating demonstration <strong>of</strong> reproduction in the higher basidiomycetes. By using several<br />

MiniFarms simultaneously, it is also possible to illustrate phototropism, geotropism, atmospheric control <strong>of</strong><br />

basidiocarp morphology, mass sporulation, and many other phenomena (including the culinary abilities <strong>of</strong> the<br />

instructor! J<br />

The following varieties are presently available: Shiitake (Lentinus edodes), Tree-Oyster (Pleurotus ostreatus ).<br />

Price: 516.95 each, ppd.; substantial discount for full cases.<br />

Please order well in advance. Specify desired week <strong>of</strong> arrival and date <strong>of</strong> class demonstration. Thank you!<br />

FAR WEST FUNGI<br />

PO Box 1333 ( M Goleta, CA 931 16<br />

Your support <strong>of</strong> this business aids and abets a graduate student in mycology.


5 4<br />

CHANGES OF AFFILIATION OR ST9TUS<br />

SHANNON M. BERCH will continue work on mycorrhi zae when she takes up her position as assistant<br />

pr<strong>of</strong>essor, Department <strong>of</strong> Soil Science, University <strong>of</strong> British Columbia, Vancouver, Canada<br />

on September 1, <strong>1985</strong>.<br />

JEAN R. BOISE, having completed her Yuseum Internship at New York, will move to Farlow<br />

Herbarium to work with Don Pfister on the Early <strong>Mycological</strong> Literature Project.<br />

THOYAS E. CHASE will be joining Jim Van Etten's laboratory in the Dept. <strong>of</strong> Plant Pathology at<br />

the University <strong>of</strong> Nebraska, in Lincoln, NE, at the end <strong>of</strong> August to work on viruses that<br />

infect Chlorell a--1 i ke Algae.<br />

LINDA Y. YOHN will assume an assistant pr<strong>of</strong>essorship in the Botany Department, University <strong>of</strong><br />

Toronto, Erindale College as a NSERC University Research Fellow on July 1, <strong>1985</strong>.<br />

SANDRA NEEDHAM, was recently appointed Curator <strong>of</strong> the Canadian Culture Collection <strong>of</strong> Fungi and<br />

Non-medical Bacteria, housed at the Biosystematics Research Institute, Agriculture Canada,<br />

Ottawa. This is a new position in the Yycology Section. Previously, the position <strong>of</strong><br />

Curator was a part-time responsibility for one <strong>of</strong> the B.R.I. mycologists.<br />

GREGORY M. MUELLER has accepted a position as Assistant Curator <strong>of</strong> Botany (Mycology) at the<br />

Field Museum <strong>of</strong> Natural History in Chicago beginning August 1, <strong>1985</strong>.<br />

ZAMIR K. PUNJA, formerly visiting assistant pr<strong>of</strong>essor, Dept. <strong>of</strong> Plant Pathology, North Carol ina<br />

State University, Raleigh, is now a Research Scientist with the Campbell Soup Company,<br />

Davis, CA.<br />

WAYNE LANIER is now Research Director at Siosis, a biological pest control company. Qiosis<br />

research projects are aimed at developing new biorational pest-control agents; emphasis is<br />

on the use <strong>of</strong> organisms already present in the soil, rather than "engineering" novel<br />

strains. See Funqi Wanted for more.<br />

LINDA J. SPIELMAN is now a Research Associate, Department <strong>of</strong> Environmental and Forest Biology,<br />

SUNY College <strong>of</strong> Environmental Science and Forestry, Syracuse, New York.<br />

J. PRESTON ALEXANDER is now at the University <strong>of</strong> Oregon Health Sciences Center in Portland; he<br />

also maintains a workspace at Portland State University.<br />

HAROLD J. LARSEN moved to western Colorado as <strong>of</strong> 4pri.l 1, <strong>1985</strong>, to become the orchard tree and<br />

fruit path01 ogist for Colorado State University and the Department <strong>of</strong> Horticulture.<br />

GERARD C. 4DAYS joined Michigan State University as an Assistant Pr<strong>of</strong>essor in the Department<br />

Botany and Plant Path01 ogy in September 1984.<br />

MICHAEL F. DOYLE will begin study for Ph.D. degree at Rancho Santa Ana Botanic Garden in<br />

September, <strong>1985</strong>.<br />

WANG YUN will be returning to China at the end <strong>of</strong> July <strong>1985</strong> where he will begin work on<br />

hypogeous fungi in China.<br />

HELP THE EDITOR (PLEASE). IN ORDER TO INCREASE OUR EFFECTIVENESS IN PREPARING THE NEWSLETTER,<br />

I ENCOURAGE OUR READERS TO CONSIDER THE FOLLOWING POINTS WHEN PREPARING MATERIAL FOR SUBMISSION<br />

TO THE EDITOR ON THE NEWSLETTER QUESTIONNIARE: (A) WRITE NEATLY AND CLEARLY (PLEASE), (B) USE<br />

PREVIOUS ISSUES ASA GUIDE TO FORMAT, CONTENT, AND DEPTH, AND (C) MAIL THE QUESTIONNAIRE WITH<br />

SUFFICIENT TIME TO REACH THE EDITOR BY THE DEADINE (MANYARE CURRENTLY ARRIVING 5-/2 DAYS AFTER<br />

THE DEADLINE) .


PAPERS, SEMINARS,<br />

SYMPOSIA, AND WORKSHOPS<br />

55<br />

KARL LEO BRAUN JR. made a film and slide presentation on the Myxomycetes, on Varch 21, to the<br />

Glen Helen Association, Yellow Springs, Ohio.<br />

The mycological group at INIREB and in related institutions (Univ. <strong>of</strong> Yorelos, Ilniv. <strong>of</strong><br />

Guadalajara, Univ. <strong>of</strong> Baja--CA, and Univ. <strong>of</strong> Metropol i tana) has 16 young mycologists<br />

working on the myc<strong>of</strong>lora <strong>of</strong> Mexico. In two years they have pub1 ished 25 papers.<br />

CLETUS P. KURTZMAN gave a seminar on "Molecular Taxonomy <strong>of</strong> the Fungi" and visited at the Plant<br />

Pathology Dept., University <strong>of</strong> Illinois at Urbana, in February <strong>1985</strong>.<br />

ORSON Y. YILLER JR. presented a lecture on "The Fungi <strong>of</strong> Western Australia" to the New York<br />

Mycol ogical <strong>Society</strong> in March.<br />

ROYALL T. MOORE presented a paper entitled "Neohaplont analysis <strong>of</strong> the basidiomycete anamorph<br />

~ntrom~co~si s broussonetiae" to the annual veeti ng <strong>of</strong> the Irish ~otanists,-queens llniv.,<br />

Belfast, Ireland on April 3, <strong>1985</strong>.<br />

Sir EDWARD ABRAHAM presented a lecture on "Historical Aspects <strong>of</strong> Penicillins and<br />

Cephalosporins", at the University <strong>of</strong> Wisconsin on May 8.<br />

FREDERICK W. SPIEGEL presented seminars at Ohio IJni versi ty, University <strong>of</strong> Southwestern<br />

Louisiana, and Louisiana State University this past year.<br />

STEVEN L. STEPHENSOI4 gave a seminar "Myxomycete Ecology" to the Department <strong>of</strong> Plant Pathology,<br />

West Virginia University on March 20, <strong>1985</strong>.<br />

JAMES !4. TRAPPE presented "Ectomycorrhizae <strong>of</strong> Leucaena and Cajanus" workshop on biological<br />

nitrogen fixation, Indo-U.S. Science & Techno1 ogy Initiative Program, New Del hi, on March<br />

27; and "Ecological interactions <strong>of</strong> fungi, mammals and trees" at the University <strong>of</strong><br />

Yarburg, Germany, April 1.<br />

RORERT C. ULLRICH presented a paper "Transforming Sasidiomycetes" at the April 13-19 UCLA<br />

Symposium on Molecul ar Biology <strong>of</strong> Filamentous Fungi.<br />

LUNG-CHI NU, presented an invited seminar on the biology <strong>of</strong> cultivated mushrooms at the<br />

University <strong>of</strong> Toledo, Department <strong>of</strong> Biology, February 22. He also led a round table<br />

discussion on current research on developmental biology <strong>of</strong> higher fungi prior to the<br />

seminar.<br />

C. W. HESSELTINE presented a symposium paper entitled "Fermented Foods" at the <strong>America</strong>n Oil<br />

Chemists' <strong>Society</strong> meeting May 6 in Philadelphia, PA. This was one <strong>of</strong> four papers devoted<br />

to vegetable proteins. He will a1 so present the keynote address "Global Significance <strong>of</strong><br />

Yycotoxins" at the International Union <strong>of</strong> Pure and Applied Chemistry meeting July 23 in<br />

Pretoria, South Africa.<br />

GERALDINE C. KAYE presented a paper "J. B. Ell is, Pioneer ~lycologist" at the Northeastern<br />

Mycologists' spring meeting at the New York State Museum, Albany, NY on April 20.<br />

DONALD H. PFISTEK presented "Mycology Universities and 19th Century Science" to the New England<br />

Mycol ogi sts.<br />

A. L. J. COLE presented a seminar entitled "Mycology and Plant Pathology in the Antipodes" to<br />

the Deparatment <strong>of</strong> Botany at Auburn University.<br />

A MUSHRUMMAGE SALE - A KERBARIUM CLEAN OUT


HONORS, AWARDS,<br />

AND PROMOTIONS<br />

LINDA M. YOHN was awarded one <strong>of</strong> fifty University Research Fellowships by the Natural Sciences<br />

and Engineering Research Council <strong>of</strong> Canada.<br />

P. K. DUBLISH was elected Fellow <strong>of</strong> the Indian Phytopathological <strong>Society</strong>.<br />

TIM BEGAN was given the Voigt Natural History <strong>of</strong> Plants Award from Southern Illinois University<br />

in Carbondal e.<br />

EVERETT S. BENEKE received the President's Certificate <strong>of</strong> Appreciation presented by the Medical<br />

<strong>Mycological</strong> <strong>Society</strong> <strong>of</strong> the <strong>America</strong>s in recognition .<strong>of</strong> outstanding support and commitment<br />

to the organization at the annual YMSA banquet on March 2, <strong>1985</strong>.<br />

JAMES F. WHITE, JR. received a Sigma Xi research award, and has been advanced to candidacy for<br />

the Ph.D. degree in mycology under Dr. G. T. Cole's supervision.<br />

ANDREW S.<br />

METHVEN and MICHAEL DOYLE have been nominated for the Honor <strong>Society</strong> <strong>of</strong> Phi Kappa Phi.<br />

STEPHEN A. REHNER received grants from Sigma Xi, University <strong>of</strong> Washington Graduate School , and<br />

NSF (Dissertation Improvement Grant) in support <strong>of</strong> dissertation research. He was also the<br />

recipient <strong>of</strong> The <strong>1985</strong> Student Award from the Puget Sound <strong>Mycological</strong> <strong>Society</strong>.<br />

IRA F. SALKIN was recently promoted from Research Scientist I V (G-27) to Research Scientist V<br />

(6-31). He was a1 so selected to serve as representative <strong>of</strong> the Medical Yycological<br />

<strong>Society</strong> <strong>of</strong> the <strong>America</strong>s to the <strong>Mycological</strong> <strong>Society</strong> <strong>of</strong> <strong>America</strong>.<br />

CARROLL W. DODGE was awarded a medal for "Meritorious Contributions to bledical Mycology" by the<br />

Medical <strong>Mycological</strong> <strong>Society</strong> <strong>of</strong> the <strong>America</strong>s on March 2, <strong>1985</strong>.<br />

ING. BENJAMIN AGUILAR <strong>of</strong> the Inst. Politecnico Nacional at Mexico City is the President <strong>of</strong> the<br />

Mexican <strong>Society</strong> <strong>of</strong> Mycology (<strong>1985</strong>-1986). G. GUZMAN continues as the President <strong>of</strong> the<br />

Editorial Board.<br />

BRYCE KENDRICK has been appointed Associate Dean <strong>of</strong> Graduate Studies at the University <strong>of</strong><br />

Waterloo, and has also been appointed Honorary Secretary <strong>of</strong> The Academy <strong>of</strong> Science <strong>of</strong> The<br />

Royal <strong>Society</strong> <strong>of</strong> Canada. He informs us that he accepted these two appointments only<br />

because he now has a full-time secretary!!<br />

CHRISTOPHER BEST was given the Best Student Paper Award by the Rotany Section at the Illinois<br />

State Academy <strong>of</strong> Science annual meeting in April for his presentation on mycorrhizal root<br />

frequency in acid and non-acid revegetated strip mine spoils.<br />

KENNETH B.<br />

1984.<br />

RAPER was elected Honorary Member <strong>of</strong> the British <strong>Mycological</strong> <strong>Society</strong> in Autumn <strong>of</strong><br />

JOHN S. KARLING, former Head <strong>of</strong> the Department <strong>of</strong> Biological Sciences, Purdue University and<br />

John Wright Distinguished Research Pr<strong>of</strong>essor <strong>of</strong> Bi 01 ogy, Emeritus, has been elected a<br />

Fellow <strong>of</strong> The Royal <strong>Society</strong> <strong>of</strong> Arts, London. A special Yarling Distinguished Lectureship<br />

in biology has been established in his honor at Purdue University.<br />

TERRENCE M.<br />

<strong>1985</strong>.<br />

HAMMILL received the SUNY Chancellor's Award for Excellence in Teaching in May<br />

MOSELIO SCHAECHTER, president <strong>of</strong> FRIENDS <strong>of</strong> the FARLOW and Bulletin Editor for the Boston<br />

~ycological Club, has added to his collection <strong>of</strong> titles that <strong>of</strong> President <strong>of</strong> the <strong>America</strong>n<br />

<strong>Society</strong> <strong>of</strong> Microbiology for <strong>1985</strong>. We expect him to raise the mycological consciousness <strong>of</strong><br />

the 34,000 members <strong>of</strong> ASM!


MICHAEL F. DOYLE was awarded the first <strong>America</strong>n <strong>Society</strong> <strong>of</strong> Plant Taxonomists Graduate Student<br />

Herbarium Travel Grant to enhance his work on a preliminary agaric flora <strong>of</strong> the Hawaiian<br />

Is1 ands.<br />

57<br />

PERSONAL NEWS<br />

EUGENE W. SMITH, who was a first time grandfather as <strong>of</strong> February <strong>1985</strong>, will be retiring from<br />

teaching in June <strong>1985</strong>.<br />

DAVE MINTER announces the birth <strong>of</strong> William John Ynox 'Yinter on November 19, 1984.<br />

SCOTT and JUDY REDHEAD are happy to announce the adoption <strong>of</strong> their third child, Ramona, age 2,<br />

maki ng 1 ife busy indeed.<br />

Sarah Emily Spiegel was born to CHRISTIE and FRED SPIEGEL on April 18, <strong>1985</strong>.<br />

ROBERT and ANGELA BELT <strong>of</strong> Albany, C4, announce the birth <strong>of</strong> their second son, David Andrew, on<br />

May 2, <strong>1985</strong>.<br />

We regret to report the following death:<br />

NORYA L. CASHION was involved in a fatal auto accident in Mexico City on December 15, 1984. A<br />

native <strong>of</strong> South Carol ina, she received her undergraduate degree from Furman University and<br />

her graduate degrees from the University <strong>of</strong> Georgia. In 1983, Dr. Cashion received her<br />

Ph.D. from the Department <strong>of</strong> Plant Pathology under the direction <strong>of</strong> E. S. Luttrell. After<br />

graduation she joined the wheat improvement program at CIMMYT, and had recently been<br />

transferred to the corn improvement program.<br />

ASSOCIATIONS AND CLUBS<br />

These enthusiastic groups form grassroots types <strong>of</strong> mycological organizations which provide<br />

education, enjoyment, edification, and edibles for many. A number <strong>of</strong> these groups are<br />

affiliated with the MSA (see page 61); this involves joining the <strong>Society</strong> on the same terms as a<br />

Personal Member, i.e., dues <strong>of</strong> $25.00, and receipt <strong>of</strong> MYCOLOGIA and the semi-annual MSA<br />

NEWSLETTER.<br />

THE ROSTON MYCOLOGICAL CLUB has just printed a Frequency <strong>of</strong> Occurence Study for 250 species<br />

<strong>of</strong> fungi. This work, which covers the New England area and represents data obtained during the<br />

17-week annual collecting season over a period <strong>of</strong> 20 years, consists <strong>of</strong> 24 pages <strong>of</strong> text and 250<br />

graphs. Each graph illustrates the frequency <strong>of</strong> a single species on a week by week basis.<br />

Price: $4.00, postaged included. Write to: Ron Trial, 98 Pembroke Street, Boston, MA 02118.<br />

Several clubs, including the SAN FRANCISCO MYCOLOGICAL SOCIETY, are currently enhancing the<br />

dialogue, both pro and con, on the subject <strong>of</strong> hunting wild mushrooms for commercial preparation<br />

and/or sale. , Ecological impact, potenti a1 health and/or safety regulation by governmental<br />

agencies, and licensing (for commercial purposes) <strong>of</strong> wild mushroom pickers are some <strong>of</strong> the<br />

issues currently bei ng addressed by individuals, clubs, and government.<br />

A MUSHRHOMB - AN EQUILATERAL MUSHROOM


5 8<br />

NOTES AND COMMENTS<br />

ON ANNOTATING SPECIMENS<br />

Amy Y. Rossman <strong>of</strong>fers the following comments and suggestions on the proper annotation <strong>of</strong><br />

herbarium specimens.<br />

Whenever a borrowed specimen is examined microscopically, it should be annotated. This is<br />

particularly true <strong>of</strong> the type specimens which are partially destroyed in the process <strong>of</strong><br />

microscopic examination; each worker has thi s obl igation to future mycol ogists. (The micros1 ide<br />

<strong>of</strong> type material must be returned with the specimen!)<br />

1. Write your evaluation <strong>of</strong> the materi a1 on special annotation slips or small pieces <strong>of</strong> paper,<br />

preferably paper with a high rag content. This slip will be permanently included with the<br />

specimen.<br />

2. WRITE LEGIBLY! If your annotation is not legible or is so cryptically abbreviated that no<br />

one can crack the code, your words are worthless.<br />

3. Use a pen with permanent ink or pencil .<br />

4. Write the specimen number or note something about the specimen on the annotation slip so<br />

that if separated, the specimen and slip can be reunited.<br />

5. Place the annotation slip inside the packet or attach it to the packet with a paper clip.<br />

Do not glue the slip to the packet or sheet.<br />

A FOREIGN VISITOR AWARD<br />

P. K. Dub1 ish informs us that every year, one MSA member outside the IJSA will be selected<br />

to visit various laboratories in <strong>America</strong> at the expense <strong>of</strong> the Indian Phytopathological<br />

<strong>Society</strong>. Duration <strong>of</strong> the visits are yet to be decided, and funding source(s) are currently<br />

bei ng devel oped.<br />

SUMMARY--YID-ATLANTIC<br />

STATES MYCOLOGY CONFERENCE<br />

The Mid-At1 antic States Yycol ogy Conference was held at George Mason University in<br />

Fairfax, Virginia May 4-5. Thirty mycologists from the region met for a day <strong>of</strong> contributed<br />

papers followed by a foray. The featured speaker was Amy Rossman from the Mycology Laboratory<br />

<strong>of</strong> the Agricultural Research Service at Beltsville, MD. She spoke on her recent Smithsonian<br />

Institution-sponsored trip to study micr<strong>of</strong>ungi in tropical southern Venezuela. The 1986<br />

conference is scheduled for Yay. See Calendar for more.<br />

SPECIMENS TEMPORARILY UNAVAILABLE<br />

During the installation <strong>of</strong> compactors, 15 April <strong>1985</strong> to about 31 March 1986, the<br />

<strong>Mycological</strong> and Vascular Plant Herbaria <strong>of</strong> the Biosystematics Research Institute, Agriculture<br />

Canada (DAO, DAOM) specimens will be moved into storage and will not be available for<br />

consul tation. For further information contact: J. A. Parmelee, Curator, Yycol ogical Herbarium,<br />

or W. J. Cody, Curator, Vascular Plant Herbarium.<br />

HELP, PLEASE<br />

Don Prusso, has specimens collected by Gilman Waldee, J. H. Standen, and G. R. Swank from<br />

1936-1938 in "North Woods". He would appreciate hearing from someone who has knowledge <strong>of</strong> the<br />

location <strong>of</strong> "North Woods".<br />

To grace the walls <strong>of</strong> his lab, Terry W. Hill is interested in obtaining a picture <strong>of</strong> Anton<br />

de Bary or, if no originals can be found, any information on where such a picture may be<br />

available (perhaps as a frontispiece?) for making a photographic copy. See Changes <strong>of</strong> Address.


J. Preston Alexander would like to know <strong>of</strong> attempts and results <strong>of</strong> efforts to culture the<br />

following: Ramaria botrytis, Calvatia gigantea, Sparassis radicata, and Herecium abietes. He<br />

would also like any information on the toxicity <strong>of</strong> Ygaricus subrufescens.<br />

From Oavid Minter: "I'm fascinated by an intriguing social phenomenon: in the U. Y. many<br />

gardens ha= plastic gnomes in them, sitting on 1 ittle plastic toadstools. Stan Hughes (pers.<br />

comm. i .e., over c<strong>of</strong>fee one day at CMI!) tell s me that in North <strong>America</strong> there are 1 ittle<br />

plastic jockeys in gardens, not gnomes!! What I want to know is this: do North <strong>America</strong>n<br />

plastic garden jockeys sit on toadstools too? Come on, <strong>America</strong>n readers, rally round, and find<br />

me the answer!"<br />

HOW TO MAKE DRIED CllLTURES<br />

Several articles have been pub1 ished on how to make dried cultures. 411 require specially<br />

manufactured boxes or slide containers. Amy Y. Rossman suggests this handy way to make dried<br />

cultures from materials always present in the laboratory.<br />

Cut one or two strips <strong>of</strong> agar with the fungus from a Petri plate to a size that will fit<br />

in the slide compartment <strong>of</strong> a single or a double slide mailer. Glue the strips into the mailer<br />

using water-soluble glue such as herbarium or Elmer's glue and let it dry. If the agar is<br />

thick, you may need to prop the lid <strong>of</strong> the mailer open until the agar dries down. Recause agar<br />

is mostly water it always dries very thin thus allowing you to close the cover <strong>of</strong> the slide<br />

mailer and protect any delicate structures that protrude above the surface <strong>of</strong> the agar.<br />

I routinely make dried cultures <strong>of</strong> isolates derived from single ascospores or those that<br />

are currently sporulating but may change with time and transferring. Dried cultures should be<br />

made as vouchers for future identification. Dried specimens are required for types <strong>of</strong> species;<br />

thus, even if a fungus is known primarily as a living culture, a dried culture must be<br />

deposited as a type specimen.<br />

A SINGLE SPORE ISOLATION TECHNIgUE<br />

For those struggling with single-spore isolations, Amy Y. Rossman <strong>of</strong>fers the following<br />

advice.<br />

Rehydrate the specimen with sterile water (usually only a minute or two is necessary).<br />

Pick <strong>of</strong>f pereithecia or other fungal material and place in a drop <strong>of</strong> sterile water in a hanging<br />

drop slide that has been sterilized. I keep hanging drop slides in a jar <strong>of</strong> alcohol and flame<br />

them as needed. Smush (love that description--ed.) the fungal material thoroughly in the drop<br />

<strong>of</strong> water with a not-so-fine needle so that the spores are outside the asci, separated from each<br />

other, and floating freely around in the water. Knock the drop <strong>of</strong> water from the slide onto a<br />

plate <strong>of</strong> agar (I use CMD + antibiotics). Smear the drop around with the flamed rounded end <strong>of</strong><br />

a testube. Don't bother to smear them to the edges <strong>of</strong> the Petri plate; picking spores from<br />

that area is difficult.<br />

The next day look for germinated spores with the 50x lens <strong>of</strong> the dissecting microscope<br />

using transmitted light. Pick <strong>of</strong>f single and/or mass germinated spores with an insect pin<br />

inserted into a needle holder and transfer them to agar plates with routinely-used media. I<br />

always make a slide with 4-6 germinated spores in order to make sure that the germinated spores<br />

are those I want.<br />

FRIENDS OF THE FARLOW WANT YOU!<br />

The Library and Herbarium <strong>of</strong> the Farlow, at Harvard University, house one <strong>of</strong> the world's<br />

most complete coll ections <strong>of</strong> materials related to systematic mycology (and 1 ichenology,<br />

bryology, and phycology as we1 1 ). FRIENDS <strong>of</strong> the FARLOW is an international group <strong>of</strong> amateur<br />

and pr<strong>of</strong>essional botanists concerned with supporting the programs and resources <strong>of</strong> the Farlow.<br />

Members receive a discount on Farlow publications, participate in book sales and other events,<br />

have speci a1 rates for photocopies <strong>of</strong> 1 i brary materi a1 s, and receive a semiannual News1 etter.<br />

Yembership categories are: Associate member, $5-815; Full member, $25; Sponsor, $50-1000;


60<br />

Benefactor, over $1000. Contributions are tax-deductible. For more information please contact<br />

Farlow Reference Library & Herbaruim <strong>of</strong> Cryptogamic Botany, Harvard University, 20 Divinity<br />

Avenue, Cambridge, MA 02138. Phone: (617) 495-2368.<br />

CHANGES OF ADDRESS FOR RESPONDENCE<br />

The following individuals have moved or changed address since the printing <strong>of</strong> the 1984 YSA<br />

Directory and are requesting response to an announcement with this issue <strong>of</strong> the MSA Newsletter.<br />

Please make these changes in your Directory as they will not appear in future Newsletter<br />

issues.<br />

Gerard C. Adams, Dept. <strong>of</strong> Botany & Plant Pathology, Michigan State University, East Lansing, MI<br />

48824.<br />

J. Preston Alexander, Rt. 1, Box 158, Forest Grove, OR 97116.<br />

Feter R. Reckjord, Dept. <strong>of</strong> Horticulture, University <strong>of</strong> Maryland, College Park, YD 20742.<br />

David Bermudes, Boston University, Dept. <strong>of</strong> Biology, 2 Cumrnington St., Boston, MA 02215.<br />

Richard L. Slanton, Dept. <strong>of</strong> Botany, Univ. <strong>of</strong> Texas, Austin, TX 78713.<br />

Jean R. Boise, Farlow Herbarium, Harvard Univ., Cambridge, MA 02138.<br />

Michael Caste1 1 ano, Forestry Sciences Laboratory, Corval 1 is, OR 97331.<br />

Benjamin H. Davis, Rldg. 25, Apt. 6, Quails Run Blvd., Englewood, FL 33533.<br />

- Kent Diebol t, 48-D Plant Science Rldg., Cornell Univ., Ithaca, NY 14853.<br />

- Michael F. Doyle (after September 1, <strong>1985</strong>), Rancho Santa Ana Botanic Garden, 1500 North College<br />

Avenue, Cl aremont , CA 91771.<br />

Terry W. Hill, Dept. <strong>of</strong> Biology, Rhodes College, 2000 North Parkway, Memphis, TN 38112.<br />

Teresi ta Iturri aga, Apartado 62018, Caracas-Venezuel a.<br />

Richard W. Yerrigan, Dept. <strong>of</strong> Biological Sciences, University <strong>of</strong> California, Santa Barbara, CA<br />

93106.<br />

Linda M. Kohn, Dept. <strong>of</strong> Botany, Univ. <strong>of</strong> Toronto, Erindale College, Mississauga, Ontario L5L<br />

1C6. Canada.<br />

Hananya J. Kronenberg, 1418 NW 179th St., Ridgefield, WA 98642.<br />

Harold J. Larsen, Orchard Mesa Research Center, 3168 0-112 Road, Grand Junction, CO 81501.<br />

-<br />

John F. Lesl ie, Dept . <strong>of</strong> Pl ant Path01 ogy, Kansas State Uni versi ty, Throckmorton Hal 1 ,<br />

Manhattan, KS 66506.<br />

John M. YcPartland, 4800 S. Lake Park #1701A, Chicago, IL 60615.<br />

Gregory Mueller (after August 1, <strong>1985</strong>), Dept. <strong>of</strong> Rotany, Field Museum <strong>of</strong> Natural History,<br />

Chicago, IL 60605-2496.<br />

Machiel E. Woordeloos, Ri jksherbarium, Schelpenkade 6, P. 0. Box 9514, NL 2300 RA, Leiden,<br />

Nether1 ands.<br />

- Stephen L. Peele, Curator, Florida Vycology Research Center, P. 0. Box 8104, Pensacola, FL<br />

32505.<br />

Jacques Pfi ster, Uni versi te de Lausanrie, Insti tut de botanique systematique, Ratiment de<br />

Biol ogie, CH - 1015, Lausanne, Swi tzerl and.<br />

Zamir K. Punja, Campbell Institute for Research and Technology, Sox 1314, Route 1, Davis, CA<br />

95616.<br />

- Elmer L. Schmidt, Dept. <strong>of</strong> Forest Products, University <strong>of</strong> P!innesota, 2004 Folwell , St. Paul , MN<br />

55108.<br />

Richard E. Scott, Division or Biochemistry, Dept. <strong>of</strong> Chemistry, Univ. <strong>of</strong> Calgary, Calgary,<br />

Alberta, Canada T2N 1N4. After September <strong>1985</strong>: Section <strong>of</strong> Clinical Chemistry, Department<br />

<strong>of</strong> Laboratory Medicine, Yayo Cl inic, Rochester, MN 55905.<br />

Mark Spear, Sylvan Spawn Laboratory Inc., West Hi1 1 s Industrial Park, Kittanning, PA 16201.<br />

Linda J. Spielman, Department <strong>of</strong> Environmental and Forest Biology, State University <strong>of</strong> New York<br />

Coll ege <strong>of</strong> Envi ronmental Science and Forestry, Syracuse, NY 13210. Phone: (315)<br />

470-6786.<br />

Wang Yun, Institute <strong>of</strong> Forestry & Soil Science, Academia Sinica, Shenyang, China (P.R.C.) .<br />

Wenying Zhuang, Dept. <strong>of</strong> Plant Pathology, Cornell Univ., Ithaca, NY 14853.


AFFILIATED SOCIETIES<br />

The Boston <strong>Mycological</strong> Club, c/o E. H. Halliwell, 855 Commonwealth Avenue,<br />

Newton, MA 02159<br />

Colorado <strong>Mycological</strong> <strong>Society</strong>, Joan L.<br />

Parkway, Denver, CO 80220<br />

Setz, Secretary, 501 Clermont<br />

The <strong>Mycological</strong> <strong>Society</strong> <strong>of</strong> San Francisco, Steve Cochrane, President, P. 0.<br />

Box 11321, San Francisco, CA 94101<br />

The North <strong>America</strong>n Yycological Association,. Gary Linc<strong>of</strong>f, President, New<br />

York Botanical Garden, Bronx, NY 10458<br />

The Ohio Mushroom <strong>Society</strong>, 288 E. North Avenue, East Palestine, OH 44413<br />

Societe Mycologique de France, 36 Rue Ge<strong>of</strong>froy-Ste. Hilaire, Paris V,<br />

France<br />

THE MYCOLOGICAL SOCETY OF AMERICA<br />

AppWcalion for Membersh4p<br />

NAME:<br />

MAIUNG ADDRESS:<br />

ZIP CODE:<br />

TELEPHONE (include area code):<br />

AREA OF INTEREST (check one)<br />

Taxonomy-Morphology<br />

- Ecology-Pathology<br />

- Physiology-Biochemistry<br />

- Cytology-Genetics<br />

Date on which you wish your membership to begin: January 1,19<br />

Signature <strong>of</strong> member endorsing your application:<br />

DUES INFORMATION (check one)<br />

- Associate Member .... S 5.00<br />

(Newsletter only)<br />

- Regular Member ...... $25.00<br />

(Includes MYCOLOGIA and Newsletter)<br />

- Student Member ...... $12.00<br />

- Emeritus Member with<br />

MYCOLOGIA ........ $12.00<br />

(Maximum eligibility - Syears) - Affiliated <strong>Society</strong> ..... $25.00<br />

Completed form and dues are to be sent to Dr, Amv Rossman. Treasurer. National Fungus<br />

Collections, %om 313. Bldg. 01 1A. 8ARC-West. Beltsville. MD 20705. PHONE: (301) 344.3366.<br />

In the U.K. send payment to Dr. David Minter. CMI. Ferry Lane. Kew. Richmond. Surrev. TW9 3AF.


WALTER J. SUNDBERG, EDITOR<br />

MYCOLOGICAL SOCIETY OF AMERICA NEWSLETTER<br />

DEPARTMENT OF BOTANY<br />

SOUTHERN ILLINOIS UNIVERSITY<br />

CARBONDALE, ILLINOIS 62901<br />

USA<br />

#<br />

4<br />

NONPROFIT ORG.<br />

U.S. POSTAGE<br />

PAID<br />

PERMIT NO. 15<br />

CARBONDALE, IL<br />

ROGER GOOS<br />

: DEPTo OF BOTANY<br />

' UNIV* OF RHOOE IS,<br />

KJNGSTON, RoI. 02881

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