The paper pondshell is found in the Mississippi River drainage, the middle St. Lawrence river drainage, the Rio Grande River system in Texas and the Ochlockonee River system in Florida. In its eastern range U. imbecillis is also found in the Altamaha River system in Georgia north to the Chowan River system, and the Gunpowder River system in Maryland.
In Michigan this species is found in Lake Erie and the Clinton, Huron, St. Joseph (Maumee River), the Grand and Kalamazoo Rivers, and the Saginaw River system, as well as lakes in these systems. (Burch, 1975)
On the Huron it was found mainly in the upper portion of the river. In general it is usually found in ponds, lakes, or mud-bottomed pools of creeks and rivers. (Cummings and Mayer, 1992; van der Schalie, 1938)
The paper pondshell is up to 10 cm (4 inches) long , and is oblong and elongate in shape. The shell is usually fairly thin and compressed in younger individuals, inflated in older individuals. The anterior end is rounded, the posterior end somewhat pointed. Dorsally, posterior margin is straight. The ventral margin is straight to moderately rounded.
Umbos are flattened, are not above the hinge line, and are situated anteriorly. The beak sculpture is fine, with two or three double-looped ridges followed by fine concentric lines.
The periostracum (outer shell layer) is shiny and smooth except for growth lines. The shell is yellow in younger individuals. Older individuals are yellow on the umbo, the rest of the shell being greenish occasionally with fine green rays, and the posterior slope is black.
On the inner shell, both valves lack pseudocardinal and lateral teeth. The beak cavity is shallow to moderately deep. Although the nacre is white, silvery or bluish-white and is iridescent at the posterior end.
In Michigan, this species can be confused with the cylindrical papershell, giant floater and creeper. All these species have umbos slightly above the hinge line. The cylindrical papershell often has a slight pinch in the middle and is slightly more inflated. The giant floater is slightly more rounded. The creeper has a small pseudocardinal tooth or swelling. (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.
Utterbackia imbecillis is a long-term brooder. In the Huron, it was gravid from late July to early June, and the spawning season is probably June to July.
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; Watters, 1995)
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 paper pondshell 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. (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. (Arey, 1921; 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 metamorphosis 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 other lab trials, glochidia metamorphosed on the spotfin shiner, greenthroat darter, yellow perch and the banded killifish. Utterbackia imbecillis has also metamorphosed on non-fish species (the tiger salamander and bullfrog) as well as non-native fish species (not listed here). (Hoeh and Trdan, 1985; Hove, et al., 1995; Howells, 1997; Parker, et al., 1980; Stern and Felder, 1978; Trdan and Hoeh, 1982; Watters and O'Dee, 1997)
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.
This species was formerly known as Anodonta imbecillis.
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.
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.
Hove, M., R. Engelking, E. Long, M. Peteler, E. Peterson. 1995. Anodontoides ferussacianus and Anodonta imbecillis host suitability tests. Triannual Unionid Report, 6: 1.
Howells, R. 1997. New fish hosts for nine freshwater mussels (Bivalvia: Unionidae) in Texas. Texas Journal of Science, 49: 255-258.
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.
Parker, R., M. Vidrine, C. Hackney. 1980. A new centrarchid host for the paper pond shell, Anodonta imbecillis Say (Bivalvia: Unionidae). ASB (Association of Southeast Biologists) Bulletin, 27: 54-55.
Stern, E., D. Felder. 1978. Identification of host fishes for four species of freshwater mussels (Bivalvia: Unionidae). American Midland Naturalist, 100: 233-236.
Trdan, R., W. Hoeh. 1982. Eurytopic host use by two congeneric species of freshwater mussel (Pelecypoda: Unionidae: Anodonta). American Midland Naturalist, 108: 381-388.
Watters, G. 1995. A guide to the freshwater mussels of Ohio. Columbus, Ohio: Ohio Department of Natural Resources.
Watters, G., S. O'Dee. 1997. Surrogate hosts: transformation on exotic and non-piscine hosts. Triannual Unionid Report, 11: 35. Accessed October 04, 2005 at http://ellipse.inhs.uiuc.edu/FMCS/TUR/TUR11.2.html.
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.