Physa acuta Draparnaud, 1805

Diagnostic features

Physa acuta can be distinguished by its completely smooth shell and mottled mantle which can usually be readily seen through the semi-transparent shell. The animal has digitations (finger-like processes) along the mantle edge against the columella and there is no false gill (pseudobranch). Unlike planorbids, the animal, if damaged when alive, does not produce red blood.

Classification

Physa acuta Draparnaud, 1805

Common name: Acute bladder snail, fountain snail

Class Gastropoda

Infraclass Heterobranchia

Megaorder Hygrophila

Order Lymnaeida

Superfamily Planorboidea

Family Physidae

Subfamily: Physinae

Genus Physa  Draparnaud, 1801 (Type species Bulla fontinalis Linnaeus, 1758) (Synonyms  Physella Haldeman, 1842 (Type species Physa globosa Haldeman, 1842); Haitia Clench & Aguayo, 1932 (Type species: Physa (Haitia) elegans Clench & Aguayo, 1932). For a list of additional synonyms see http://www.marinespecies.org/aphia.php?p=taxdetails&id=160462).

Original name: Physa acuta Draparnaud, 1805. In Draparnaud, J. P. R. (1805). Histoire Naturelle des Mollusques Terrestres et Fluviatiles de la France.  Paris : L. Colas, i-viii, 1-164 pp.

Type locality: Garonne River, France (introduced from North America).

SynonymsLymnaea heterostropha Say, 1825 and several others - see http://www.marinespecies.org/aphia.php?p=taxdetails&id=234093

State of taxonomy

This introduced species is often referred to as Physella acuta or sometimes Haitia acuta in the literature. Taylor (2003) transferred Physa acuta to the genus Haitia Clench & Aguayo, 1932 and this was followed in an earlier version of this key.

Biology and ecology

On water weeds, rocks, wood and other vegetation in rivers, streams, ponds, swamps, drains, ditches and similar habitats. Very pollution tolerant and may even be found in sewerage treatment plants. Often abundant. Feeds on algae and detritus. Egg mass a kidney-shaped jelly strip containing many small eggs. Development direct.

P. acuta is the host of the fluke Choanocotyle hobbsi in the Murray-Darling system (Barton et al. 2022).

Distribution

Worldwide. Native to north-eastern United States and adjacent Canada. P. acuta has been introduced widely, and is now in Europe, Asia Minor, Africa, the Mascarene and Macaronesian Islands, India, Nepal, marginal East Asia, Australia, New Zealand, Polynesia, Brasil and Argentina.

Introduced to Australia, probably from North America or Europe. Occurs throughout much of Australia, mainly (but not exclusively) in coastal drainages in agricultural and urban areas where it is usually abundant.

Notes

This introduced species is abundant in many waterways in temperate Australia and is often referred to as Physella acuta or sometimes Haitia acuta.

Physa is easily confused with species of Glyptophysa (Planorbidae) which have similar-shaped, sinistral shells. Physa can be distinguished by its completely smooth shell (Glyptophysa often - but not always - has some periostracal ornament) and mottled mantle which can usually be readily seen through the semi-transparent shell (Glyptophysa has a uniformly dark-coloured mantle). The animal also has digitations (finger-like processes) along the mantle edge against the columella (smooth in Glyptophysa) and there is no false gill (pseudobranch) (present in Glyptophysa). The animal, if damaged when alive, does not produce coloured blood, whereas Glyptophysa has red- coloured blood.

Species of Isidorella should also be compared, but differ from Physa in the same characters given above for Glyptophysa.

Physa mexicana (Philippi in Küster, 1841) - also from North America - is widespread throughout the world as well and is indistinguishable from P. acuta in shell morphology however P. acuta differs in the elongate sarcobelum in the reproductive system which is a feature not seen in P. mexicana (Taylor, 2003)  Because of the similarity of both species it is currently unknown if P. mexicana is present in Australia. Other species such as Physa gyrina (Say, 1821) could also possibly be undetected.

Further reading

Barton, D. P., Zhu, X., Nuhoglu, A., Pearce, L., McLellan, M., & Shamsi, S. (2022). Parasites of selected freshwater snails in the eastern Murray Darling Basin, Australia. International Journal of Environmental Research and Public Health 19(12): 7236 (1-16).

Beesley, P. L., Ross, G. J. B. & Wells, A., Eds. (1998). Mollusca: The Southern Synthesis. Parts A & B. Melbourne, CSIRO Publishing.

Bousset, L., Pointier, J. P., David, P. & Jarne, P. (2014). Neither variation loss, nor change in selfing rate is associated with the worldwide invasion of Physa acuta from its native North America. Biological Invasions 16: 1769-1783.

Campbell, N. J. (1977). Identifying liver fluke snails. Agricultural Gazette of New South Wales 88: 24-26.

Cieplok, A. & Spyra, A. (2020). The roles of spatial and environmental variables in the appearance of a globally invasive Physa acuta in water bodies created due to human activity. Science of the Total Environment 744: 140928.

Clampitt, P. T. 1970. Comparative ecology of the snails Physa gyrina and Physa integra (Basommatophora: Physidae). Malacologia 10: 113-151.

Clench, W. J. & Aguayo, C. G. (1932). Proceedings of the New England Zoological Club 13: 37.

Cope, N. J. & Winterbourn, M. J. (2004). Competitive interactions between two successful molluscan invaders of freshwaters: an experimental study. Aquatic Ecology 38: 83-91.

Dillon, R. T., Wethington, A. R., Rhett, J. M. & Smith, T. P. (2002). Populations of the European freshwater pulmonate Physa acuta are not reproductively isolated from American Physa heterostropha or Physa integra. Invertebrate Biology 121: 226-234.

Dillon, R. T., Wethington, A. R. & Lydeard, C. (2011). The evolution of reproductive isolation in a simultaneous hermaphrodite, the freshwater snail Physa. BMC Evolutionary Biology 11: 1-12.

Dobson, M. (2004). Replacement of native freshwater snails by the exotic Physa acuta (Gastropoda: Physidae) in southern Mozambique; a possible control mechanism for schistosomiasis. Annals of Tropical Medicine & Parasitology 98: 543-548.

Duncan, C. J. (1958). The anatomy and physiology of the reproductive system of the freshwater snail Physa fontinalis. Proceedings of the Zoological Society of London 131: 55-84.

Ebbs, E. T., Loker, E. S. & Brant, S. V. (2018) Phylogeography and genetics of the globally invasive snail Physa acuta Draparnaud 1805, and its potential to serve as an intermediate host to larval digenetic trematodes. BMC Evolutionary Biology 18: 1-17.

Gregoric, D.E. G., de Lucía, M., Torres, S. H., Copa, J. L. E. & Darrigran, G. (2024). Invasive freshwater gastropods in South America: Physa acuta and its expansion to Austral Patagonia in Argentina. Papéis Avulsos de Zoologia 64: e202464029-e202464029.

Jenkins, M. K. (1991). The decline of floodplain gastropod populations in the Lower River Murray, with reference to Glyptophysa connica (Walker 1988 (sic!)) and Physa acuta (Draparnaud 1805). Thesis, BSc Hon., Dept. of Zoology, Univ. of Adelaide.

Kershaw, R. C. (1991). Snail and Slug Pests of Tasmania, Queen Victoria Museum and Art Gallery, Launceston.

Leeuwen, C. H. van , Huig, N., Van der Velde, G., Van Alen, T. A., Wagemaker, C. A., Sherman, C. D., Klaassen, M. & Figuerola, J. (2013). How did this snail get here? Several dispersal vectors inferred for an aquatic invasive species. Freshwater Biology 58: 88-99.

Lydeard, C., Campbell, D. & Golz, M. (2016). Physa acuta Draparnaud, 1805 should be treated as a native of North America, not Europe. Malacologia 59: 347-350.

Mitchell, D. R. & Leung, T. L. F. (2016). Sharing the load: a survey of parasitism in the invasive freshwater pulmonate, Physa acuta (Hygrophila: Physidae) and sympatric native snail populations. Hydrobiologia 766: 165-172.

Ng, T.H., Tan, S.K., Wong, W.H., Meier, R., Chan, S-Y., Tan, H.H. and Yeo, D.C.J. 2016. Molluscs for Sale: Assessment of Freshwater Gastropods and Bivalves in the Ornamental Pet Trade. PLOS One. DOI:10.1371/journal.pone.0161130.

Ohbayashi-Hodoki, K., Ishihama, F. & Shimada, M. (2004). Body size–dependent gender role in a simultaneous hermaphrodite freshwater snail, Physa acuta. Behavioral Ecology 15: 976-981.

Perrin, N. (1986). Les paramètres du cyde vital de Physa acuta (Gastropoda, Mollusca) en milieu experimental. Revue Suisse de Zoologie 93:725- 736.

Ponder, W. F., Clark, S. A. & Dallwitz, M. J. (2000). Freshwater and estuarine molluscs: an interactive, illustrated key for New South Wales. Melbourne, CSIRO Publishing.

Shea, M. (1995). Freshwater molluscs of Sydney. Australian Shell News 88: 4-6.

Smith, B. J. and Kershaw, R. C. (1979). Field guide to the non-marine molluscs of south eastern Australia. Australian National University Press, Canberra, Australia.

Smith, B. J. & Kershaw, R. C. (1981). Tasmanian Land and Freshwater Molluscs. Hobart, University of Tasmania.

Tariel, J., Luquet, É. & Plénet, S. (2020). Interactions between maternal, paternal, developmental, and immediate environmental effects on anti-predator behavior of the snail Physa acuta. Frontiers in Ecology and Evolution 8: 591074.

Taylor D. W. (2003). Introduction to Physidae (Gastropoda: Hygrophila). Biology, classification, morphology. Revista de Biología Tropical (International Journal of Tropical Biology and Conservation) 51(Supplement 1): 1-299.

Wethington, A. R. & Lydeard, C. (2007). A molecular phylogeny of Physidae (Gastropoda: Basommatophora) based on mitochondrial DNA sequences. Journal of Molluscan Studies 73: 241-257.

Wethington, A. R., Wise, J. & Dillon, R. T. (2009). Genetic and morphological characterization of the Physidae of South Carolina (Gastropoda: Pulmonata: Basommatophora), with description of a new species. Nautilus 123: 282-292.

Wethington, A. R. & Lydeard, C. (2019). Physidae Fitzinger, 1833. Pp. 175-180 in C. Lydeard & Cummings, K. S. Freshwater Mollusks of the World: a Distribution Atlas. Baltimore, John Hopkins University Press.

Zukowski, S., Walker, K. F. 2009 Freshwater snails in competition: alien Physa acuta (Physidae) and native Glyptophysa gibbosa (Planorbidae) in the River Murray, South Australia, Marine and Freshwater Research, 60: 999-1005.