Alasmidonta viridis

Geographic Range

The slippershell is found in the upper Mississippi drainage, and in Ohio Cumberland and Tennessee Rivers. In the St. Lawrence system it is found from Lake Huron to the Ottawa River. In general its range extends from western Maine, south to northern Georgia, west to Arkansas and north to North Dakota.

In Michigan this species is found in smaller creeks and rivers in both the upper and lower peninsula.

• Biogeographic Regions
• nearctic nearctic
  • native native

Habitat

This species is found in creeks and small rivers. Usually it needs fairly good quality water and is found buried in sand and gravel.

• Habitat Regions
• freshwater freshwater

• Aquatic Biomes
• rivers and streams

Physical Description

The slippershell is up to 3.8 cm (1.5 inches) long , and is rhomboidal. Older individuals have fairly thick shells. The anterior end is rounded, the posterior end square and truncated above and sharply rounded below. The dorsal margin is slightly rounded and the ventral margin is straight or slightly arched.

Umbos are raised slightly above the hinge line. The beak sculpture is three to six irregular loops.

The periostracum (outer shell layer) is smooth to rough, yellow-green to yellow-brown with wavy green rays.

On the inner shell, the left valve has two triangular pseudocardinal teeth. The right valve has one single, serrated squarish pseudocardinal tooth. Usually lateral teeth are just thickened areas, but occasionally double teeth are in the left valve.

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

In Michigan, this species can be confused with the elktoe. The slippershell is smaller (therefore has closer growth lines) and lacks the dark blue dots found on the elktoe shell.

• Other Physical Features
• ectothermic ectothermic
• heterothermic heterothermic
• bilateral symmetry bilateral symmetry

• Sexual Dimorphism
• sexes alike

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.

• Development - Life Cycle
• metamorphosis metamorphosis

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.

Alasmidonta viridis is a long-term brooder. In the Huron River in Michigan, it was gravid from early August through late April of the following spring. It probably breeds in early May to July in Michigan.

• Key Reproductive Features
• seasonal breeding seasonal breeding
• gonochoric/gonochoristic/dioecious (sexes separate)
• sexual sexual
• fertilization fertilization
  • internal internal
• viviparous viviparous

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. Often the slippershells are found buried under the substrate.

• Key Behaviors
• parasite parasite
• motile motile
• sedentary sedentary

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. How the slippershell attracts or if it recognizes its fish host is unknown.

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.

• Communication Channels
• chemical chemical

• Perception Channels
• visual visual
• tactile tactile
• vibrations vibrations
• chemical chemical

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.

• Primary Diet
• planktivore planktivore
• detritivore detritivore

• Plant Foods
• algae
• phytoplankton phytoplankton

• Other Foods
• detritus detritus
• microbes

• Foraging Behavior
• filter-feeding filter-feeding

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.

Ecosystem Roles

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

• Ecosystem Impact
• parasite parasite

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

Alasmidonta viridis is on endangered lists in Alabama, Iowa, North Carolina, and Virginia. In Illinois and Wisconsin it is considered threatened, and in Michigan it is a species of special concern.

Other Comments

Alasmidonta viridis is synonymous with Alasmidonta calceolus .

Additional Links

Encyclopedia of Life

Contributors

Renee Sherman Mulcrone (author).

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.

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 .

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. 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.

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.