Mainly an Atlantic coast species, the eastern ellliptio is found in the Apalachicola river system, Altamaha River system of Georgia north to the St. Lawrence River system of Canada. In the Interior Basin it is found west to Lake Superior and within the Hudson Bay drainage.
The eastern elliptio is mainly found in stable shoals of lakes or river-lakes in the northern part of the lower peninsula and the upper peninsula. It was most abundant in substrates composed of clay mixed with marl and fine sand, but rarely in mud. Depths where it seemed most common were one to 1.6 m (3 to 5 feet). (Matteson, 1948c; van der Schalie, 1938)
The eastern elliptio is up to 12.5 cm (5 inches) long , and is quadrate or rectangular in shape. The shell is heavy and compressed with an angular posterior ridge and prominent posterior slope. The anterior end is rounded, the posterior end rounded to bluntly pointed. The dorsal margin is straight and the ventral margin is straight to slightly curved.
Umbos are low, being raised only slightly above the hinge line. The beak sculpture has 5-6 ridges.
The periostracum (outer shell layer) is tan or brown, sometimes with green rays. Older specimens tend to be more brown or black.
On the inner shell, the left valve has two pseudocardinal teeth, which are triangular and rough. The two lateral teeth are straight to slightly curved and moderately long. The right valve has one triangular, rough pseudocardinal tooth, and one straight to slightly curved, long, lateral tooth.
The beak cavity is shallow. The nacre is purple, rose-colored or white.
In Michigan, this species can be confused with the spike. The eastern ellipse is slightly more rhomboidal, more compressed, and has a slightly more prominent posterior ridge. (Cordeiro, 2003; Nedeau, et al., 2000)
Fertilized eggs are brooded in the marsupia (water tubes) up to one months, depending on environmental conditions, 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 glochida 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; Matteson, 1948c)
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 fertilized in the suprabranchial chambers, then pass into water tubes of the gills, where they develop into larvae, called glochidia. (Lefevre and Curtis, 1912; 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.
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 they are found 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.
Unionids in general may have some form of chemical reception to recognize fish hosts. Mantle flaps in the lampsilines are modified to attract potential fish hosts. How the snuffbox attracts its main fish host, the logperch, is unknown. However, the mantle flaps are darkened and may resemble food for the logperch.
Glochidia respond to both touch, light and some chemical cues. In general, when touched or a fluid is introduced, they will respond by clamping shut. (Arey, 1921; Brusca and Brusca, 2003; Watters, 1995)
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. (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.
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 transformations 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, green sunfish, the largemouth bass, the orangespotted sunfish, and the white crappie. (Cummings and Watters, 2004; Lefevre and Curtis, 1912; Matteson, 1948c; Matteson, 1955; Tedla and Fernando, 1969; Young, 1911)metamorphosed on the
Mussels are ecological indicators. Their presence in a water body usually indicates good water quality.
This species is not on any federal or state lists.
Elliptio complanatus.is synonomous with
An detailed life history of this species was done by Max Matteson in the early 1940s in northern Michigan. (Matteson, 1948c)
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.
Brusca, R., G. Brusca. 2003. Invertebrates. Sunderland, Massachusetts: Sinauer Associates, Inc..
Burch, J. 1975. Freshwater unionacean clams (Mollusca: Pelecypoda) of North America. Hamburg, Michigan: Malacological Publications.
Cordeiro, J. 2003. "Family Unionidae: Genus Elliptio" (On-line). Freshwater mussels of the New York metropolitan region and New Jersey, A guide to their identification, biology, and conservation. Accessed September 05, 2006 at http://cbc.amnh.org/mussel/elliptiogenustext.html.
Cummings, K., C. Mayer. 1992. Field guide to freshwater mussels of the Midwest. Champaign, Illinois: Illinois Natural History Survey Manual 5. Accessed August 25, 2005 at http://www.inhs.uiuc.edu/cbd/collections/mollusk/fieldguide.html.
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 25, 2005 at http://184.108.40.206/Musselhost/.
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.
Matteson, M. 1948. The taxonomic and distributional history of the fresh-water mussel Elliptio complanatus (Dillwyn, 1817). Nautilus, 61: 127-132.
Matteson, M. 1948. The taxonomic and distributional history of the fresh-water mussel Elliptio complanatus (Dillwyn, 1817) (continued). Nautilus, 62: 13-1.
Matteson, M. 1948. Life history of Elliptio complanatus (Dillwyn, 1817). American Midland Naturalist, 40: 690-723.
Matteson, M. 1955. Studies on the natural history of the Unionidae. American Midland Naturalist, 53: 126-145.
Nedeau, E., M. McCollough, B. Swartz. 2000. The freshwater mussels of Maine. Augusta, Maine: Maine Dept. of Insland Fisheries and Wildlife.
Oesch, R. 1984. Missouri naiades, a guide to the mussels of Missouri. Jefferson City, Missouri: Missouri Department of Conservation.
Tedla, S., C. Fernando. 1969. Observations on the glochidia of Lampsilis radiata (Gmelin) infesting yellow perch, Perca flavescens (Mitchill) in the Bay of Quinte, Lake Ontario. Canadian Journal of Zoology, 47: 705-712.
Watters, G. 1995. A guide to the freshwater mussels of Ohio. Columbus, Ohio: Ohio Department of Natural Resources.
Young, D. 1911. The implantation of the glochidium on the fish. Univerity of Missouri Bulletin Science Series, 2: 1-20.
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.