Unionidae

The Unionidae are a family of freshwater mussels, the largest in the order Unionida, the bivalve molluscs sometimes known as river mussels, or simply as unionids.[1][2]

Unionidae
Six endangered species of Unionidae
Scientific classification
Kingdom: Animalia
Phylum: Mollusca
Class: Bivalvia
Order: Unionida
Superfamily: Unionoidea
Family: Unionidae
Fleming, 1828
Genera

See text

The range of distribution for this family is world-wide. It is at its most diverse in North America, with about 297 recognised taxa,[3][4][5] but China and Southeast Asia also support very diverse faunas.

Freshwater mussels occupy a wide range of habitats, but most often occupy lotic waters, i.e. flowing water such as rivers, streams and creeks.

Origin and early diversification

The recent phylogenetic study reveals that the Unionidae most likely originated in Southeast and East Asia in the Jurassic, with the earliest expansions into North America and Africa (since the mid-Cretaceous) followed by the colonization of Europe and India (since the Paleocene).[6]

Life history

Unionidae burrow into the substrate, with their posterior margins exposed. They pump water through the incurrent aperture, obtaining oxygen and food. They remove phytoplankton and zooplankton, as well as suspended bacteria, fungal spores, and dissolved organic matter.[7][8][9][10][11][12][13][14][15][16] Despite extensive laboratory studies, which of these filtrates unionoids actually process remains uncertain. In high densities, they have the ability to influence water clarity [17][18] but filtration rates are dependent on water temperature, current velocity, and particle size and concentration. In addition, gill morphology can determine particle size filtered, as well as the rate.[11]

Reproduction

Unionidae are distinguished by a unique and complex lifecycle. Most unionids are of separate sex, although some species, such as Elliptio complanata, are known to be hermaphroditic.[19]

The sperm is ejected from the mantle cavity through the male’s excurrent aperture and taken into the female's mantle cavity through the incurrent aperture. Fertilised eggs move from the gonads to the gills (marsupia) where they further ripen and metamorph into glochidia, the first larval stage. Mature glochidia are released by the female and then attach to the gills, fins, or skin of a host fish. A cyst is quickly formed around the glochidia, and they stay on the fish for several weeks or months before they fall off as juvenile mussels, which then bury themselves in the sediment.

Some of the species in the Unionidae, commonly known as pocketbook mussels, have evolved a remarkable reproductive strategy. The edge of the female's body that protrudes from the valves of the shell develops into an imitation of a small fish complete with markings and false eyes. This decoy moves in the current and attracts the attention of real fish. Some fish see the decoy as prey, while others see a conspecific, i.e. a member of their own species. Whatever they see, they approach for a closer look and the mussel releases huge numbers of larvae from her gills, dousing the inquisitive fish with her tiny, parasitic young. These glochidial larvae are drawn into the fish's gills, where they attach and trigger a tissue response that forms a small cyst in which the young mussel resides. It feeds by breaking down and digesting the tissue of the fish within the cyst.[20]

Sex is determined by a region located on the mitochondrial DNA, the male open-reading frame (M-ORF) and female open-reading frame (F-ORF). Hermaphroditic mussels lack these regions and contain a female-like open-reading frame dubbed hermaphroditic open-reading frame (H-ORF). In many mussels, the hermaphroditic state is ancestral and the male sex evolved later. This region of the mitochondria also may be responsible for the evolution of doubly uniparental inheritance seen in freshwater mussels.[21]

Genera

Fossilization and taphonomic implications

In large enough quantities, unionid shells can have enough of an impact on environmental conditions to affect the ability of organic remains in the local environment to fossilize.[22] For example, in the Dinosaur Park Formation, fossil hadrosaur eggshell is rare[22] because the breakdown of tannins from local coniferous vegetation would have caused the ancient waters to become acidic.[22] Eggshell fragments are present in only two microfossil sites, both of which are dominated by the preserved shells of invertebrate life, including unionids.[22] The slow dissolution of these shells releasing calcium carbonate into the water raised the water's pH high enough to prevent the eggshell fragments from dissolving before they could be fossilized.[22]

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References
  1. Unionidae. Retrieved through: World Register of Marine Species on 4 January 2012.
  2. Huber, Markus (2010). Compendium of Bivalves. A Full-color Guide to 3'300 of the World's Marine Bivalves. A Status on Bivalvia after 250 Years of Research. Hackenheim: ConchBooks. pp. 901 pp. + CD. ISBN 978-3-939767-28-2.
  3. Williams, J. D, M. L. Warren, K. S. Cummings, J. L. Harris, and R. J. Neves (1993). "Conservation Status of Freshwater Mussels of the United States and Canada". Fisheries. 18 (9): 6–22. doi:10.1577/1548-8446(1993)018<0006:CSOFMO>2.0.CO;2. ISSN 1548-8446.CS1 maint: multiple names: authors list (link)
  4. Burch, John B.. 1975. Freshwater unionacean clams (Mollusca: Pelecypoda) of North America. Biota of Freshwater Ecosystems, Identification Manual No. 11. U.S. Gov. Printing Office. 114p.
  5. Heard, William H. 1979. Identification Manual of the Freshwater Clams of Florida. Fla. Dept. Environmental Regulation, Technical Series 4(2): 1-83.
  6. Bolotov, I.N., Kondakov, A.V., Vikhrev, I.V., Aksenova, O.V., Bespalaya, Y.V. Gofarov, M.Y., Kolosova, Y.S., Konopleva, E.S., Spitsyn, V.M., Tanmuangpak, K. & Tumpeesuwan, S. (2017). Ancient River Inference Explains Exceptional Oriental Freshwater Mussel Radiations.Scientific Reports 7: 2135, doi:10.1038/s41598-017-02312-z
  7. Allan, W. R. (1914). "The food and feeding habits of freshwater mussels." Biological Bulletin 27: 127-147.
  8. Coker, R. E., Shira, A.F., Clark, H.W., Howard, A.D. (1921). "Natural history and propagation of fresh-water mussels." Bulletin of the Bureau of Fisheries 37: 77-181.
  9. Churchill, E. P., Lewis, S.I. (1924). "Food and feeding in fresh-water mussels." Bulletin of the Bureau of Fisheries 39: 439-471.
  10. McMahon, R. F., Bogan, A.E. (2001). Mollusca: Bivalvia. Ecology and classification of North American freshwater invertebrates. J. H. Thorp, Covich, A.P. San Diego, Academic Press: 331-429.
  11. Silverman, H., Nichols S.J, Cherry J.S., Archberger E., Lynn J.S., Dietz T.H. (1997). "Clearance of laboratory-cultured bacteria by freshwater bivalves: differences between lentic and lotic unionids." Canadian Journal of Zoology 75: 1857-1866.
  12. Bärlocher, F., Brendelberger, H. (2004). "Clearance of aquatic hyphomycete spores by a benthic suspension feeder." Limnology and Oceanography 49: 2292-2296.
  13. Roditi, H. A., Fisher, N.S., Sanudo-Wilhelmy, S.A. (2002). "Uptake of dissolved organic carbon and trace elements by zebra mussels." Nature 407: 78-80.
  14. Baines, S. B., Fisher, N.S., Cole, J.J. (2005). "Uptake of dissolved organic matter (DOM) and its importance to metabolic requirements of the zebra mussel, Dreissena polymorpha." Limnology and Oceanography 50: 36-47.
  15. Yeager, M. M., Cherry, D.S., Neves, R.J. (1994). "Feeding and burrowing behaviors of juvenile rainbow mussels, Villosa iris (Bivalvia, Unionidae)." Journal of the North American Benthological Society 133: 217-222.
  16. Nichols, S. J., Silverman, H. Dietx, T.H., Lynn, J.W., Garling, D.L. (2005). "Pathways of food uptake in native (Unionidae) and introduced (Corbiculidae and Dreissenidae) freshwater bivalves." Journal of Great Lakes Research 31: 87-96.
  17. Cohen, R. R. H., Dresler, P.V., Phillips, E.P.J., Cory, R.L. (1984). "The effects of the Asiatic clam, Corbicula fluminea, on phytoplankton of the Potomac River, Maryland." Limnology and Oceanography 29: 170-180.
  18. Phelps, H. L. (1994). "The Asiatic clam (Corbicula fluminea): invasion and system-level ecological change in the Potomac River estuary near Washington, D.C." Estuaries 17: 614-621.
  19. Downing, J. A., Amyot, J.P., Pérusse, M., Rochon, Y. (1989). "Visceral sex, hermaphroditism, and protandry in a population of the freshwater bivalve Elliptio complanata." Journal of the North American Benthological Society 8(1): 92-99.
  20. Piper, Ross (2007), Extraordinary Animals: An Encyclopedia of Curious and Unusual Animals, Greenwood Press.
  21. Breton, S., Stewart, Donald T., Shepardson, Sally, Trdan, Richard J., Bogan, Arthur E., Chapman, Eric G., Ruminas, Adrew J., Piontkivska, Helen, Hoeh, Walter R. (2011). "Novel Protein Genes in Animal mtDNA: A New Sex Determination System in Freshwater Mussels (Bivalvia: Unionoida)?" Molecular Biology and Evolution 28(5): 1645-1659.
  22. Tanke, D.H. and Brett-Surman, M.K. 2001. Evidence of Hatchling and Nestling-Size Hadrosaurs (Reptilia:Ornithischia) from Dinosaur Provincial Park (Dinosaur Park Formation: Campanian), Alberta, Canada. pp. 206-218. In: Mesozoic Vertebrate Life—New Research Inspired by the Paleontology of Philip J. Currie. Edited by D.H. Tanke and K. Carpenter. Indiana University Press: Bloomington. xviii + 577 pp.
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