Skip to main content
Log in

Palustriella falcata (Brid.) Hedenäs (Amblystegiaceae, Bryopsida) with pluristratose lamina: morphological variability of specimens in springs of the Italian Alps

  • Original Article
  • Published:
Plant Systematics and Evolution Aims and scope Submit manuscript

Abstract

Pluristratose leaf lamina in pleurocarpous aquatic mosses is a mysterious morphological character state because of its recurrence among unrelated lineages. It has been found sporadically around the world in phylogenetically distant taxa, and is thought to be a mutation and/or adaptation to aquatic habitats. During an extensive survey of bryophytes in spring habitats in the Italian Alps (Province of Trento), we found different numbers of leaf lamina cell layers among specimens of Palustriella falcata. We carried out a thorough study, measuring a set of morphological characters that identify variability among specimens within the same spring and among multiple springs. The main goals were to assess the amount of morphological variability, to quantify the concordance among morphological traits, and to test to what extent environmental variables account for morphological variability. Our results showed that, in many cases, morphological characters differed even among shoots within a spring. We found positive and significant partial correlation between pluristratose lamina and width of costa, but negative correlation between pluristratose lamina and length of cells. Constrained multivariate analysis showed that 40.3% of this morphological variation was explained by a set of environmental variables, but most importantly, we observed extensive pluristratose laminae in constantly submerged habitats. We interpreted the different numbers of cell layers in the leaf lamina as a phenotypic continuum from P. falcata, with a single layer of cells, to Palustriella pluristratosa Stech & Frahm, with a multilayered lamina. In addition we offer a point of view concerning the evolutionary significance of this trait, its possible origin, and its evolution in aquatic mosses.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  • APHA (2000) Standard methods for the examination of water and wastewater. American Public Health Association, Washington

    Google Scholar 

  • Barrett SCH, Eckert CG, Husband BC (1993) Evolutionary processes in aquatic plant populations. Aquat Bot 44:105–145

    Article  Google Scholar 

  • Beever JE, Fife AJ (2008) Hypnobartlettia fontana is an environmental form of Cratoneuropsis relaxa (Bryophyta: Amblystegiaceae). N Z J Bot 46:341–345

    Google Scholar 

  • Buryova B, Shaw AJ (2005) Phenotypic plasticity in Philonotis fontana (Bryopsida: Bartramiaceae). J Bryol 27:13–22

    Article  Google Scholar 

  • Cantonati M, Gerecke R, Bertuzzi E (2006) Springs of the Alps, sensitive ecosystems to environmental change: from biodiversity assessments to long-term studies. Hydrobiologia 562:59–96

    Article  CAS  Google Scholar 

  • Ernande B, Dieckmann U (2004) The evolution of phenotypic plasticity in spatially structured environments: implications of intraspecific competition, plasticity costs and environmental characteristics. J Evol Biol 17:613–628

    Article  CAS  PubMed  Google Scholar 

  • Ghalambor CK, McKay JH, Carroll SP, Reznick DN (2007) Adaptive versus non-adaptive phenotypic plasticity and the potential for contemporary adaptation in new environments. Funct Ecol 21:394–407

    Article  Google Scholar 

  • Glime JM, Vitt DH (1984) The physiological adaptations of aquatic Musci. Lindbergia 10:41–52

    Google Scholar 

  • Gordon ND, McMahon TA, Finlayson BL, Gippel CJ, Nathan RJ (2004) Stream hydrology: an introduction for ecologists, 2nd edn. Wiley, West Sussex

    Google Scholar 

  • Hedenäs L (1993) Field and microscope keys to the Fennoscandian species of the CalliergonScorpidiumDrepanocladus complex, including some related or similar species. Biodetektor, Märsta

    Google Scholar 

  • Hedenäs L (2001) Environmental factors potentially affecting character states in pleurocarpous mosses. Bryologist 104:72–91

    Article  Google Scholar 

  • Hedenäs L (2003) The European species of the CalliergonScorpidiumDrepanocladus complex, including some related or similar species. Meylania 28:1–116

    Google Scholar 

  • Hedenäs L (2008) Molecular variation in Drepanocladus aduncus s.l. does not support recognition of more than one species in Europe. J Bryol 30:108–120

    Article  Google Scholar 

  • Hedenäs L, Kooijman A (2004) Habitat differentiation within Palustriella. Lindbergia 29:40–50

    Google Scholar 

  • Legendre P, Legendre L (1998) Numerical ecology, 2nd English edn., Elsevier, Amsterdam

    Google Scholar 

  • Ochyra R (1985) Hypnobartlettia fontana gen. et sp. nov. (Musci: Hypnobartlettiaceae fam. nov.), a unique moss from New Zealand. Lindbergia 11:2–8

    Google Scholar 

  • Ochyra R (1989) Animadversion on the moss genus Cratoneuron (Sull) Spruce. J Hattory Bot Lab 67:203–242

    Google Scholar 

  • Ochyra R, Vanderpoorten A (1999) Platyhypnidium mutatum, a mysterious new moss from Germany. J Bryol 21:183–189

    Google Scholar 

  • Ochyra R, Schmidt C, Bültmann H (1998) Grandstenia torrenticola, a new aquatic moss species from Tenerife. J Bryol 20:403–409

    Google Scholar 

  • Pigliucci M (2001) Phenotypic plasticity: beyond nature and nurture. Johns Hopkins University Press, Baltimore

    Google Scholar 

  • Shaw AJ (1986) A new approach to the experimental propagation of bryophytes. Taxon 35:671–675

    Article  Google Scholar 

  • Sokal RR, Rohlf FJ (1995) Biometry. WH Freeman, New York

    Google Scholar 

  • Stech M, Frahm JP (1999) The status of Platyhypnidium mutatum Ochyra R. & Vanderpoorten and the systematic value of the Donrichardsiaceae based on molecular data. J Bryol 21:191–195

    Google Scholar 

  • Stech M, Frahm JP (2001) Palustriella pluristratosa spec. nov. (Amblystegiaceae, Bryopsida), a new aquatic moss species with pluristratose lamina from Switzerland. Bot Helv 111:139–150

    Google Scholar 

  • Vanderpoorten A, Jacquemart AL (2004) Evolutionary mode, tempo, and phylogenetic association of continuous morphological traits in the aquatic moss genus Amblystegium. J Evol Biol 17:279–287

    Article  CAS  PubMed  Google Scholar 

  • Vanderpoorten A, Hedenäs L, Cox CJ, Shaw AJ (2002a) Circumscription, classification, and taxonomy of Amblystegiaceae (Bryopsida) inferred from nuclear and chloroplast DNA sequence data and morphology. Taxon 51:115–122

    Article  Google Scholar 

  • Vanderpoorten A, Hedenäs L, Cox CJ, Shaw AJ (2002b) Phylogeny and morphological evolution of the Amblystegiaceae (Bryopsida). Mol Phylogenet Evol 23:1–21

    Article  CAS  PubMed  Google Scholar 

  • Via S, Gomulkiewicz R, de Jong G, Scheiner SM, Schlichting CD, van Tienderen PH (1995) Adaptive phenotypic plasticity: consensus and controversy. Trends Ecol Evol 10:212–217

    Article  Google Scholar 

  • Vitt DH, Glime JM (1984) Structural adaptation of aquatic Musci. Linbergia 10:95–110

    Google Scholar 

  • West-Eberhard (2003) Developmental plasticity and evolution. Oxford University Press, New York

    Google Scholar 

  • Wyatt R, Stoneburner A (1980) Distribution and phenetic affinities of Donrichardsia, an endemic moss from the Edward Plateu of Texas. Bryologist 83:512–520

    Article  Google Scholar 

Download references

Acknowledgments

This work was financed by the University and Scientific Research Department of the Autonomous Province of Trento (CRENODAT Project: Biodiversity Assessment and Integrity Evaluation of Springs of Trentino—Italian Alps—and Long-Term Ecological Research, 2004–2008).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Daniel Spitale.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Spitale, D., Petraglia, A. Palustriella falcata (Brid.) Hedenäs (Amblystegiaceae, Bryopsida) with pluristratose lamina: morphological variability of specimens in springs of the Italian Alps. Plant Syst Evol 286, 59–68 (2010). https://doi.org/10.1007/s00606-010-0279-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00606-010-0279-0

Keywords

Navigation