Ligumia nasuta

Ge­o­graphic Range

The east­ern pond mus­sel is found from the James River of Vir­ginia north to the St. Lawrence drainages in Canada, west to Lake Erie, Ohio and Michi­gan.

In Michi­gan L. na­suta is found in the lower penin­sula in drainages on the east­ern side of the state. Gen­er­ally, this is a pond and lake species. (Burch, 1975; van der Schalie, 1938; Wat­ters, 1995)

Habi­tat

The east­ern pond­mus­sel is usu­ally found in lakes, ponds, or quiet wa­ters of streams. Sub­strates it in­hab­its are vari­able. In the Huron River this species was found on sandy bot­toms of quiet pools or in sandy areas of beach pools. (Cum­mings and Mayer, 1992; van der Schalie, 1938; Wat­ters, 1995)

  • Aquatic Biomes
  • rivers and streams

Phys­i­cal De­scrip­tion

The east­ern pond­mus­sel is up to 10 cm (4 inches) long , and is elon­gate in shape, usu­ally over twice as long as high. The shell is usu­ally fairly thin and com­pressed, and this species has a dis­tinct pos­te­rior ridge. The an­te­rior end is rounded, the pos­te­rior end pointed. The dor­sal mar­gin is straight and the ven­tral mar­gin is straight to curved as it .

Umbos are low, being raised only slightly above the hinge line. The beak sculp­ture has dou­ble-looped ridges.

The pe­rios­tracum (outer shell layer) is smooth, ex­cept for growth lines and tan to dark green, some­times with fine green rays. Older spec­i­mens tend to be more brown or black.

On the inner shell, the left valve has one to two pseudo­car­di­nal teeth, which are tri­an­gu­lar and del­i­cate. The two lat­eral teeth are straight and long. The right valve has one tri­an­gu­lar pseudo­car­di­nal tooth The one lat­eral is also straight and long.

The beak cav­ity is shal­low to mod­er­ately deep. Al­though the nacre is white, oc­ca­sion­ally it is has a pink or salmon tint and is iri­des­cent at the pos­te­rior end.

In Michi­gan, this species can be con­fused with the black sand­shell. The black sand­shell is more cylin­dri­cal, not as pointed pos­te­ri­orly, and is gen­er­ally larger and thicker. (Cordeiro, 2003; Nedeau, et al., 2000; Wat­ters, 1995)

  • Sexual Dimorphism
  • sexes shaped differently
  • Range length
    10 (high) cm
    3.94 (high) in

De­vel­op­ment

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)

Re­pro­duc­tion

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.

Ligu­mia na­suta is a long-term brooder. In the Huron River in Michi­gan, it was gravid from early Au­gust to late June. It prob­a­bly spawns in July in Michi­gan. (Lefevre and Cur­tis, 1912; Wat­ters, 1995)

  • Breeding interval
    The eastern pondmussel breeds once in the warmer months of the year.
  • Breeding season
    In Michigan, the breeding season is probably July.
  • Range gestation period
    11 (high) 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

Lifes­pan/Longevity

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.

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. (Oesch, 1984)

Com­mu­ni­ca­tion and Per­cep­tion

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. Man­tle flaps in the lamp­si­lines are mod­i­fied to at­tract po­ten­tial fish hosts. How the east­ern pond­mus­sel at­tracts and/or 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)

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.

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)

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

While fresh­wa­ter mus­sels re­quire a host fish for meta­mor­pho­sis, the host for the east­ern pond­mus­sel is un­known.

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

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

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

There are no sig­nif­i­cant neg­a­tive im­pacts of mus­sels on hu­mans.

Con­ser­va­tion Sta­tus

Ligu­mia na­suta is listed as En­dan­gered in Delaware and Ohio, Threat­ened in New Jer­sey and Spe­cial Con­cern in Mass­a­chu­setts. It is also a Species of Con­cern in Rhode Is­land. The IUCN Red List con­sid­ers this species Lower Risk, near Threat­ened on the IUCN Red List. (Hove, 2004)

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 Ligu­mia" (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/​ligumiagenustext.​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.

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.

Nedeau, E., M. Mc­Col­lough, B. Swartz. 2000. The fresh­wa­ter mus­sels of Maine. Au­gusta, Maine: Maine De­part­ment of In­land Fish­eries and Wildlife.

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.