occurs (regularly, as a native taxon) in multiple nations
Regularity: Regularly occurring
Type of Residency: Year-round
Regularity: Regularly occurring
Type of Residency: Year-round
Global Range: Members of this family are found throughout Europe, Asia, and in Africa, Indonesia, the Philippines and Australia. This species was introduced a long time ago to North America and has spread widely. However, it has been reported in Pleistocene deposits in Chicago so it may already have been in North America at the time of European settlement (Burch 1989).
Depth range (m): 0 - 14
Depth range (m): 0 - 14
Note: this information has not been validated. Check this *note*. Your feedback is most welcome.
Habitat Type: Freshwater
Non-Migrant: No. All populations of this species make significant seasonal migrations.
Locally Migrant: No. No populations of this species make local extended movements (generally less than 200 km) at particular times of the year (e.g., to breeding or wintering grounds, to hibernation sites).
Locally Migrant: No. No populations of this species make annual migrations of over 200 km.
Molecular Biology and Genetics
Barcode data: Bithynia tentaculata
There are 3 barcode sequences available from BOLD and GenBank. Below is a sequence of the barcode region Cytochrome oxidase subunit 1 (COI or COX1) from a member of the species. See the BOLD taxonomy browser for more complete information about this specimen and other sequences.
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Download FASTA File
Statistics of barcoding coverage: Bithynia tentaculata
Public Records: 3
Specimens with Barcodes: 9
Species With Barcodes: 1
National NatureServe Conservation Status
Rounded National Status Rank: NNA - Not Applicable
Rounded National Status Rank: NNA - Not Applicable
Bithynia tentaculata, common names the mud bithynia or common bithynia, or faucet snail is a relatively small species of freshwater snail with gills and an operculum, an aquatic prosobranch gastropod mollusk in the family Bithyniidae.
- Bithynia tentaculata f. codia
- Bithynia tentaculata f. excavata
- Bithynia tentaculata f. gigas
- Bithynia tentaculata f. producta Menke, 1828
The width of the shell is 5–7 mm.
The faucet snail has a shiny pale brown shell, oval in shape, with a relatively large and rounded spire consisting of 5–6 somewhat flattened whorls, no umbilicus, and a very thick lip. The aperture is less than half the height of the shell.
Adult Bithynia tentaculata possess a white, calcareous, tear-drop to oval-shaped operculum with distinct concentric rings. The operculum of juveniles, however, is spirally marked. The operculum (on the back of the foot) is always situated very close to the aperture of the shell. The animal itself has pointed, long tentacles and a simple foot with the right cervical lobe acting as a channel for water.
Distribution: palearctic, including:
- Czech Republic - least concern (LC)
- Germany - common species overall in Germany, but is listed as endangered (gefährdet) in Saxony and in Thuringia
- British Isles: Great Britain and Ireland
Great Lakes Region: Bithynia tentaculata was first recorded in Lake Michigan in 1871, but was probably introduced in 1870. It spread to Lake Ontario by 1879, the Hudson River by 1892, and other tributaries and water bodies in the Finger Lakes region during the 20th century. It was introduced to Lake Erie sometime before 1930. This snail’s range extends in 1992 from Quebec and Wisconsin to Pennsylvania and New York. It has been recorded from Lake Huron, but only a few individuals were found in benthic samples from Saginaw Bay in the 1980s and 1990s.
This snail lives in slow-running freshwater habitat such as low-velocity rivers, and standing-water bodies such as lakes. The species flourishes in calcium-rich waters.
It is commonly found in freshwater ponds, shallow lakes, and canals. This species is found on the substrate in fall and winter (including gravel, sand, clay, mud or undersides of rocks) and on aquatic macrophytes (including milfoil, Myriophyllum spicatum and muskgrass, Chara spp.) in warmer months.  It lives mostly in shoals, but is also found at depths of up to 5 m. Bithynia tentaculata inhabits intertidal zones in the Hudson River But in general, this snail inhabits waters with pH of 6.6–8.4, conductivity of 87–2320 μmhos/cm, Ca2+ of 5–89 ppm, and Na+ of 4–291 ppm. It can potentially survive well in water bodies with high concentrations of K+ and low concentrations of NO3-. In the Saint Lawrence River, it tends to occur in relatively unpolluted, nearshore areas and amongst dreissenid mussel beds.
This species functions as both a scraper and a collector-filterer, grazing on algae on the substrate, as well as using its gills to filter suspended algae from the water column. When filter feeding, algae is sucked in, condensed, and then passed out between the right tentacle and exhalant siphon in pellet-like packages which are then eaten. The ability to filter feed may play a role in allowing populations of the faucet snail to survive at high densities in relatively eutrophic, anthropogenically influenced water bodies. Bithynia tentaculata feeds selectively on food items. The faucet snail is known in Eurasia to feed on black fly larvae.
Bithynia tentaculata is dioecious (it has two separate sexes) and lays its eggs on rocks, wood and shells in organized aggregates arranged in double rows, in clumps of 1–77. Egg-laying occurs from May to July when water temperature is 20°C or higher, and sometimes a second time in October and November by females born early in the year. The density of eggs on the substrate can sometimes reach 155 clumps/m2. Fecundity may reach up to 347 eggs and is greatest for the 2nd year class. Eggs hatch in three weeks to three months, depending on water temperature. Oocytes develop poorly at temperatures of 30 - 34°C. Growth usually does not occur from September to May. The lifespan varies regionally and can be anywhere from 17–39 months.
The faucet snail has the potential to be a good biomonitor for contaminants such as Cd, Zn, and methylmercury (MeHg) because there are good correlations between environmental concentrations and snail tissue concentrations with respect to these toxic compounds.
- As first intermediate host for Prosthogonimus ovatus
- As an intermediate host for Sphaeridiotrema globulus
- As first intermediate hosts and as second intermediate host for Cyanthocotyle bushiensis.
- As second intermediate host for Echinostoma revolutum
- As intermediate host for Syngamus trachea
- Capillariidae, probably Capillaria obsignata
- Bithynia tenataculata is a suspected intermediate host for Leyogonimus polyoon
Other interspecific relationship
Natural dispersal of this snail is known to occur by passive transport in birds.
This article incorporates public domain text from reference.
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- Rebekah M. Kipp & Amy Benson. 2008. Bithynia tentaculata. USGS Nonindigenous Aquatic Species Database, Gainesville, FL. http://nas.er.usgs.gov/queries/FactSheet.asp?speciesID=987 Revision Date: 2/28/2007.
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- Beran L. (2009). "The first record of Anisus vorticulus (Troschel, 1834) (Gastropoda: Planorbidae) in Croatia?". Malacologica Bohemoslovaca 8: 70. PDF.
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- Bithynia tentaculata www.mollbase.de, Verbreitungsatlas Schleswig-Holstein 1991, accessed 19 October 2008.
- Bithynia tentaculata
- Mills, E.L., J.H. Leach, J.T. Carlton and C.L. Secor. 1993. Exotic species in the Great Lakes: a history of biotic crises and anthropogenic introductions. Journal of Great Lakes Research 19(1):1-54.
- Carr, J. F. and J. K. Hiltunen. 1965. Changes in the bottom fauna of western Lake Erie from 1930 to 1961. Limnology and Oceanography 10: 551-569.
- Krieger, K. A. 1985. Snail distribution in Lake Erie, USA, Canada; the influence of anoxia in the southern central basin nearshore zone. Ohio Journal of Science 85(5):230-244.
- Nalepa, T.F., D.L. Fanslow, M.B. Lansing, G.A. Lang, M. Ford, G. Gostenik and D.J. Hartson. 2002. Abundance, Biomass, and Species Composition of Benthic Macroinvertebrates Populations in Saginaw Bay, Lake Huron, 1987-1996. NOAA Great Lakes Environmental Research Laboratory and Cooperative Institute for Limnology and Ecosystem Research, Michigan, Ann Arbor. 32 pp.
- Vincent, B., H. Rioux and M. Harvey. 1981. Factors affecting the structure of epiphytic gastropod communities in the St. Lawrence River (Quebec, Canada). Hydrobiologia 220:57-71.
- Vaillancourt, G. and E. Lafarriere. 1983. Relationship between the quality of the environment and the benthic groupings in the littoral zone of the St. Lawrence River, Canada. Naturaliste Canadien (Quebec) 110(4):385-396.
- Ricciardi, A., F.G. Whoriskey, and J.B. Rasmussen. 1997. The role of the zebra mussel (Dreissena polymorpha) in structuring macroinvertebrate communities on hard substrata. Canadian Journal of Fisheries and Aquatic Sciences 54: 2596–2608.
- Brendelberger, H. 1997. Contrasting feeding strategies of two freshwater gastropods, Radix peregra (Lymnaeidae) and Bithynia tentaculata (Bithynidae). Archiv fur Hydrobiologie 140(1):1-21.
- Pavlichenko, V.I. 1977. The role of Hydropsyche angustipennis (Trichoptera: Hydropsychidae) larvae in destroying black flies in flowing reservoirs of the Zaporozyhe oblast, USSR. Ekologiya (Moscow) 1:104-105.
- Korotneva, N.V. and I.N. Dregol’skaya. 1992. Effect of the elevated temperature in the habitat of fresh water mollusk Bithynia tentaculata L. on its oogenesis. Tsitologiya 34(2):30-36.
- Desy, J.C., J.-F. Archambault, B. Pinel-Alloul, J. Hubert and P.G.C. Campbell. 2000. Relationships between total mercury in sediments and methyl mercury in the freshwater gastropod prosobranch Bithynia tentaculata in the St. Lawrence River, Quebec. Canadian Journal of Fisheries and Aquatic Sciences 57(Suppl. 1):164-173.
- Flessas, C., Y. Couillard, B. Pinel-Alloul, L. St-Cyr and P.G.C. Campbell. 2000. Metal concentrations in two freshwater gastropods (Mollusca) in the St. Lawrence River and relationships with environmental contamination. Canadian Journal of Fisheries and Aquatic Sciences 57(Suppl. 1):126-137.
- Mattison, R.G., T.S. Dunn, R.E.B. Hanna, W.A. Nizami and Q.M. Ali. 1995. Population dynamics of freshwater gastropods and epidemiology of their helminth infections with emphasis on larval parmphistomes in northern India. Journal of Helminthology 69(2):125-138.
- Morley, N. J., M. E. Adam and J. W. Lewis. 2004. The role of Bithynia tentaculata in the transmission of larval digeneans from a gravel pit in the Lower Thames Valley. Journal of Helminthology 78(2):129-135.
- Toledo, R., C. Munoz-Antoli, M. Perez and J.G. Esteban. 1998. Larval trematode infections in freshwater gastropods from the Albufera Natural Park in Spain. Journal of Helminthology 72(1):79-82.
- Prosthogonimus ovatus (Parasite Species Summary)
- Sauer, J.S., Cole, R.A., and Nissen, J.M., 2007, Finding the exotic faucet snail (Bithynia tentaculata): Investigation of waterbird die-offs on the Upper Mississippi River National Wildlife and Fish Refuge: U.S. Geological Survey Open-File Report 2007–1065, 3 p.
- Cyanthocotyle bushiensis (Parasite Species Summary)
- Echinostomum revolutum (Parasite Species Summary)
- Syngamus trachea (Parasite Species Summary)
- Chapter 35 - Miscellaneous Parasitic Diseases - Field Manual of Wildlife Diseases
- von Proschwitz, T. 1997. Bithynia tentaculata (L.) in Norway – a rare species on the edge of its western distribution, and some notes on the dispersal of freshwater snails. Fauna (Oslo) 50(3):102-107.
- Kelly, P.M. and J.S. Cory. 1987. Operculum closing as a defense against predatory leeches in four British freshwater prosobranch snails. Hydrobiologia 144(2):121-124.
|Wikimedia Commons has media related to Bithynia tentaculata.|
- Bithynia tentaculata at www.science.mcmaster.ca
- Brendelberger H.: Growth of juvenile Bithynia tentaculata (Prosobranchia, Bithyniidae) under different food regimes: a long-term laboratory study. J. Moll. Stud. (1995), 61, 89-95. (abstract)
- Shiro Tashiro, J. and S.D. Colman. 1982. Filter-feeding in the freshwater prosobranch snail Bithynia tentaculata: bioenergetic partitioning of ingested carbon and nitrogen. American Midland Naturalist 107(1): 114-132.
- PAN Pesticides Database - Chemical Toxicity Studies
- Bithynia tentaculata Species account and photograph at Mollusc Ireland.
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