The purple wartyback is found in the Mississippi drainage, the Lake St. Clair drainage, the Detroit River and Lake Erie.
The purple wartyback is up to 12.7 cm (5 inches) long, and is round. The shell is fairly thick, heavy and compressed. The anterior end is rounded, the posterior end somewhat angled. The dorsal margin is straight to slightly rounded and the ventral margin is broadly rounded. (Cummings and Mayer, 1992; Oesch, 1984; Watters, 1995)
The periostracum (outer shell layer) has several pustules, and ridges on the dorsal wing. Younger specimens are yellowish to greenish brown, while older specimens tend to be more uniformly brown. (Cummings and Mayer, 1992; Oesch, 1984; Watters, 1995)
On the inner shell, the left valve has two widely divergent, serrated, thin and low pseudocardinal teeth. The two lateral teeth are striated, and straight to slightly curved. The right valve has one heavy, triangular serrated pseudocardinal tooth with a small tooth on either side. The right, single lateral tooth is slightly curved and striated. (Cummings and Mayer, 1992; Oesch, 1984; Watters, 1995)
In Michigan, this species can be confused with the pimpleback. The pimpleback usually has a prominent green ray, lacks a dorsal wing and purple nacre. (Cummings and Mayer, 1992; Oesch, 1984; Watters, 1995)
Fertilized eggs are brooded in the marsupia (water tubes) up to three months, where they develop into larvae, called glochidia. The glochidia are then released into the water where they must attach to the gill filaments and/or general body surface of the host fish. After attachment, epithelial tissue from the host fish grows over and encapsulates the glochidium, usually within a few hours. The glochidium then metamorphoses into a juvenile mussel within a few days or weeks. After metamorphosis, the juvenile is sloughed off as a free-living organism. Juveniles are found in the substrate where they develop into adults. (Arey, 1921; Lefevre and Curtis, 1910)
Age to sexual maturity for this species is unknown. Unionids are gonochoristic (sexes are separate) and viviparous. The glochidia, which are the larval stage of the mussels, are released live from the female after they are fully developed.
In general, gametogenesis in unionids is initiated by increasing water temperatures. The general life cycle of a unionid, includes open fertilization. Males release sperm into the water, which is taken in by the females through their respiratory current. The eggs are internally fertilized in the suprabranchial chambers, then pass into water tubes of the gills, where they develop into glochidia.
The purple wartyback is a short-term brooder. On the Huron River, it was gravid from late May to early August. It likely spawns in early May. (Lefevre and Curtis, 1912; van der Schalie, 1938; Watters, 1995)
Females brood fertilized eggs in their marsupial pouch. The fertilized eggs develop into glochidia. There is no parental investment after the female releases the glochidia.
The age of mussels can be determined by looking at annual rings on the shell. However, no demographic data on this species has been recorded.
Mussels in general are rather sedentary, although they may move in response to changing water levels and conditions. Although not thoroughly documented, the mussels may vertically migrate to release glochidia and spawn. Often this species is buried under the substrate. (Oesch, 1984)
The middle lobe of the mantle edge has most of a bivalve's sensory organs. Paired statocysts, which are fluid filled chambers with a solid granule or pellet (a statolity) are in the mussel's foot. The statocysts help the mussel with georeception, or orientation.
Mussels are heterothermic, and therefore are sensitive and responsive to temperature.
Unionids in general may have some form of chemical reception to recognize fish hosts. How the purple wartyback attracts or if it recognizes its fish host is unknown.
In general, unionids are filter feeders. The mussels use cilia to pump water into the incurrent siphon where food is caught in a mucus lining in the demibranchs. Particles are sorted by the labial palps and then directed to the mouth. Mussels have been cultured on algae, but they may also ingest bacteria, protozoans and other organic particles.
The parasitic glochidial stage absorbs blood and nutrients from hosts after attachment. Mantle cells within the glochidia feed off of the host’s tissue through phagocytocis. (Arey, 1921; Meglitsch and Schram, 1991; Watters, 1995)
Unionids in general are preyed upon by muskrats, raccoons, minks, otters, and some birds. Juveniles are probably also fed upon by freshwater drum, sheepshead, lake sturgeon, spotted suckers, redhorses, and pumpkinseeds. (Cummings and Mayer, 1992; Watters, 1995)
Unionid mortality and reproduction is affected by unionicolid mites and monogenic trematodes feeding on gill and mantle tissue. Parasitic chironomid larvae may destroy up to half the mussel gill. (Cummings and Mayer, 1992; Watters, 1995)
Fish hosts are determined by looking at both lab metamorphosis and natural infestations. Looking at both is necessary, as lab transformations from glochidia to juvenile may occur, but the mussel may not actually infect a particular species in a natural situation. Natural infestations may also be found, but glochidia will attach to almost any fish, including those that are not suitable hosts. Lab transformations involve isolating one particular fish species and introducing glochidia either into the fish tank or directly inoculating the fish gills with glochidia. Tanks are monitored and if juveniles are later found the fish species is considered a suitable host.
In lab trials, black bullhead, the yellow bullhead, the channel catfish, and the flathead catfish. These species generally co-exist with the purple wartyback, but no natural infestations have been observed. (Cummings and Watters, 2004; Hove, et al., 1994; Hove, 1997; Hove, M.C., Engelking, R.A., Peteler, M.E, et al., 1997)metamorphosed on the
Mussels are ecological indicators. Their presence in a water body usually indicates good water quality.
There are no significant negative impacts of mussels on humans.
Renee Sherman Mulcrone (author).
living in the Nearctic biogeographic province, the northern part of the New World. This includes Greenland, the Canadian Arctic islands, and all of the North American as far south as the highlands of central Mexico.
having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.
uses smells or other chemicals to communicate
an animal that mainly eats decomposed plants and/or animals
particles of organic material from dead and decomposing organisms. Detritus is the result of the activity of decomposers (organisms that decompose organic material).
animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature
union of egg and spermatozoan
a method of feeding where small food particles are filtered from the surrounding water by various mechanisms. Used mainly by aquatic invertebrates, especially plankton, but also by baleen whales.
mainly lives in water that is not salty.
having a body temperature that fluctuates with that of the immediate environment; having no mechanism or a poorly developed mechanism for regulating internal body temperature.
fertilization takes place within the female's body
A large change in the shape or structure of an animal that happens as the animal grows. In insects, "incomplete metamorphosis" is when young animals are similar to adults and change gradually into the adult form, and "complete metamorphosis" is when there is a profound change between larval and adult forms. Butterflies have complete metamorphosis, grasshoppers have incomplete metamorphosis.
having the capacity to move from one place to another.
the area in which the animal is naturally found, the region in which it is endemic.
an organism that obtains nutrients from other organisms in a harmful way that doesn't cause immediate death
photosynthetic or plant constituent of plankton; mainly unicellular algae. (Compare to zooplankton.)
an animal that mainly eats plankton
breeding is confined to a particular season
remains in the same area
reproduction that includes combining the genetic contribution of two individuals, a male and a female
uses touch to communicate
movements of a hard surface that are produced by animals as signals to others
uses sight to communicate
reproduction in which fertilization and development take place within the female body and the developing embryo derives nourishment from the female.
Arey, L. 1921. An experimental study on glochidia and the factors underlying encystment. J. Exp. Zool., 33: 463-499.
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Burch, J. 1975. Freshwater unionacean clams (Mollusca: Pelecypoda) of North America. Hamburg, Michigan: Malacological Publications.
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Cummings, K., G. Watters. 2004. "Mussel/Host Data Base" (On-line). Molluscs Division of the Museum of Biological Diversity at the Ohio State University. Accessed September 24, 2005 at http://188.8.131.52/Musselhost/.
Graf, D. 2002. Historical biogeography and late glacial origin of the freshwater pearly mussel (Bivalvia: Unionidae) faunas of Lake Erie, North America. Occasional Papers of Mollusks, 6: 175-211.
Haag, W., M. Warren. 1997. Host fishes and reproductive biology of six freshwater mussel species from the Mobile Basin, USA. Journal of the North American Benthological Society, 16: 576-585.
Hoeh, W., R. Trdan. 1985. Freshwater mussels (Pelecypoda: Unionidae) of the major tributaries of the St. Clair River, Michigan. Malacological Review, 18: 115-116.
Hove, M.C., Engelking, R.A., Peteler, M.E, , Hove, M.C., Engelking, R.A., Peteler, M.E, Hove, M.C., Engelking, R.A., Peteler, M.E, Peterson, E.M., Kapuscinski, A.R., Sovell, L.A. and E.R. Evers. 1997. Suitable fish hosts for glochidia of four freshwater mussels. Conservation and Management of Freshwater Mussels II. Proceedings of a UMRCC Symposium, 16-18 October 1995, St. Louis, Missouri: 21-25. Accessed October 04, 2005 at http://ellipse.inhs.uiuc.edu/FMCS/Meetings/Symp1995Abs.html.
Hove, M. 2004. "Links to each state's listed freshwater mussels, invertebrates, or fauna" (On-line). Accessed September 21, 2005 at http://www.fw.umn.edu/Personnel/staff/Hove/State.TE.mussels.
Hove, M. 1997. Ictalurids serve as suitable hosts for the purple wartyback. Triannual unionid report, 11: 4. Accessed October 01, 2005 at http://ellipse.inhs.uiuc.edu/FMCS/TUR/TUR11.html#p4.
Hove, M., R. Engelking, E. Evers, M. Peteler, E. Peterson.. 1994. Cyclonaias tuberculata host suitability tests. Triannual unionid report, 5.
Lefevre, G., W. Curtis. 1912. Experiments in the artificial propagation of fresh-water mussels. Proc. Internat. Fishery Congress, Washington. Bull. Bur. Fisheries, 28: 617-626.
Lefevre, G., W. Curtis. 1910. Reproduction and parasitism in the Unionidae. J. Expt. Biol., 9: 79-115.
Meglitsch, P., F. Schram. 1991. Invertebrate Zoology, Third Edition. New York, NY: Oxford University Press, Inc.
Oesch, R. 1984. Missouri naiades, a guide to the mussels of Missouri. Jefferson City, Missouri: Missouri Department of Conservation.
Watters, G. 1995. A guide to the freshwater mussels of Ohio. Columbus, Ohio: Ohio Department of Natural Resources.
van der Schalie, H. 1938. The naiad fauna of the Huron River, in southeastern Michigan. Miscellaneous Publications of the Museum of Zoology, University of Michigan, 40: 1-83.