The fluted-shell is generally in the Mississippi River drainage, including the Tombigbee River system. To the north it occurs in the St. Lawrence system from north of Lake Superior to Lake Champlain and the Ottawa River. In the Hudson Bay drainage it is found in the Red and Winnipeg systems.
In general, L. costata is sporadically distributed where it is found. In Michigan the fluted shell generally occurs in small to medium sized rivers in both the upper and lower peninsulas. (Burch, 1975; van der Schalie, 1938; Watters, 1995)
The fluted shell is found in medium to large rivers, often in riffles and runs. Substrates it inhabits includes sand, mud, or fine gravel in areas with slow to moderate flow.
In the Huron it was found mainly in areas with noticeable current, with sand and gravel substrates. (Cummings and Mayer, 1992; van der Schalie, 1938; Watters, 1995)
The fluted-shell is up to 17.8 cm (7 inches) long , and is ovate and elongate in shape. The shell is moderately thick, compressed to moderately inflated. The anterior end is uniformly rounded, the posterior end is truncated above and angular where the posterior ridge meets the margin of the shell. The dorsal and ventral margins are straight to slightly curved.
Umbos are low, and not raised above the hinge line. The beak sculpture has three or four concentric and sometimes sinuate ridges.
The periostracum (outer shell layer) is smooth, and younger individuals often has green and brown rays. Older specimens tend to be more brown.
On the inner shell, the left valve has two fused pseudocardinal teeth, which are smooth. The lateral teeth is just a thickened area on the hinge line. The right valve has one (occastionally two) triangular and smooth pseudocardinal tooth.
The beak cavity is shallow. The nacre is blue-white, tinged with cream or salmon-colored at the beak cavity, and iridescent at the posterior end.
In Michigan, this species can be confused with the creek heelsplitter, which is usually smaller and lacks flutings on the wing. (Cummings and Mayer, 1992; Oesch, 1984; Watters, 1995)
Fertilized eggs are brooded in the marsupia (water tubes) up to 11 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 a glochidium, usually within a few hours. The glochidia 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.
Lasmigona compressa is a long-term brooder. In the Huron River in Michigan, it was gravid from early August to late May. It probably spawns from June to July in Michigan. (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.
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. (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 fluted shell attracts and recognizes its fish host is unknown.
Glochidia respond to 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.
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. (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.
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, Lasmigona costata metamorphosed on the banded darter, longnose dace, and northern hogsucker. (Watters, et al., 1999; Watters, et al., 1998)
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.
Lasmigona costata is listed as Endangered in Vermont, Threatened in Kansas and Special Concern in Minnesota. (Hove, 2004)
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.
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.
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.
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.
Watters, G., S. O'Dee, S. Chordas. 1998. New potential hosts for: Strophitus undulatus- Ohio River drainage; Strophitus undulatus - Susquehanna River drainage; Alasimidonta undulata - Susquehanna River drainage; Actinonaias ligamentina - Ohio River drainage; and Lasmigona costata - Ohio River drainage. Triannual Unionid Report, 15: 27-29. Accessed October 04, 2005 at http://ellipse.inhs.uiuc.edu/FMCS/TUR/TUR15.html#p21.
Watters, G., S. Chordas, S. O'Dee, J. Reiger. 1999. Host identification studies for six species of Unionidae. First Symposium of the Freshwater Mollusk Conservation Society, March 16 - 20, 1999 in Chattanooga, Tennessee: 75.
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.