Elliptio complanata

Ge­o­graphic Range

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.

In Michi­gan E. com­planata is found from Cheboy­gan County north through the upper penin­sula. In the lower penin­sula the south­ern­most records were from Lake Huron. One his­tor­i­cal record was from the Clin­ton River. (Burch, 1975; Mat­te­son, 1948a; Mat­te­son, 1948b)

Habi­tat

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)

  • Aquatic Biomes
  • rivers and streams
  • Range depth
    1.6 (high) m
    5.25 (high) ft

Phys­i­cal De­scrip­tion

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)

  • Sexual Dimorphism
  • sexes alike
  • Range length
    12.5 (high) cm
    4.92 (high) in

De­vel­op­ment

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)

Re­pro­duc­tion

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)

  • Breeding season
    In Michigan, the breeding season is mid-July to August.
  • Average gestation period
    10 months

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.

  • Parental Investment
  • pre-fertilization
    • provisioning
  • pre-hatching/birth
    • provisioning
      • female

Be­hav­ior

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)

Com­mu­ni­ca­tion and Per­cep­tion

Three large, dis­tinct gan­glia make up the bi­lat­eral ner­vous sys­tem of a bi­valve. Cere­bro­pleural gan­glia are an­te­rior and give rise to the vis­ceral (gut) gan­glia and pedal (foot) gan­glia.

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)

Food Habits

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)

Pre­da­tion

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)

Ecosys­tem Roles

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.

Lab meta­mor­pho­sis and nat­ural in­fec­tions of El­lip­tio com­planata have been ob­served for the yel­low perch and the banded kil­li­fish,.

In lab tri­als, El­lip­tio com­planata meta­mor­phosed on the 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)

Species Used as Host

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Mus­sels are eco­log­i­cal in­di­ca­tors. Their pres­ence in a water body usu­ally in­di­cates good water qual­ity.

Con­ser­va­tion Sta­tus

This species is not on any fed­eral or state lists.

Other Com­ments

El­lip­tio com­planata is syn­onomous with El­lip­tio com­plana­tus.

An de­tailed life his­tory of this species was done by Max Mat­te­son in the early 1940s in north­ern Michi­gan. (Mat­te­son, 1948c)

Con­trib­u­tors

Renee Sher­man Mul­crone (au­thor).

Glossary

Nearctic

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.

World Map

bilateral symmetry

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.

chemical

uses smells or other chemicals to communicate

detritivore

an animal that mainly eats decomposed plants and/or animals

detritus

particles of organic material from dead and decomposing organisms. Detritus is the result of the activity of decomposers (organisms that decompose organic material).

ectothermic

animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature

fertilization

union of egg and spermatozoan

filter-feeding

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.

freshwater

mainly lives in water that is not salty.

heterothermic

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.

internal fertilization

fertilization takes place within the female's body

metamorphosis

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.

motile

having the capacity to move from one place to another.

native range

the area in which the animal is naturally found, the region in which it is endemic.

parasite

an organism that obtains nutrients from other organisms in a harmful way that doesn't cause immediate death

phytoplankton

photosynthetic or plant constituent of plankton; mainly unicellular algae. (Compare to zooplankton.)

planktivore

an animal that mainly eats plankton

seasonal breeding

breeding is confined to a particular season

sedentary

remains in the same area

sexual

reproduction that includes combining the genetic contribution of two individuals, a male and a female

tactile

uses touch to communicate

vibrations

movements of a hard surface that are produced by animals as signals to others

visual

uses sight to communicate

viviparous

reproduction in which fertilization and development take place within the female body and the developing embryo derives nourishment from the female.

Ref­er­ences

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://​128.​146.​250.​63/​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.