The rainbow mussel is found in the Ohio, Tennessee and upper Mississippi river systems. In the Great Lakes it is found in drainages of Lakes Michigan, Huron, Ontario and Erie. The southern limit of this species is difficult to define because of taxonomic uncertainties of species and subspecies in the south.
Found in Michigan's lower peninsula, V. iris occurs in the Lake Michigan tributaries from the Muskegon south to the St. Joseph River on the west side of the state. On the east side of the state it is also found in the Saginaw River drainages and Lake Erie drainages. (Burch, 1975)
The rainbow is found in cool, clear, upper reaches of small to medium streams. Substrates it inhabits include sandy mud, coarse sand, or gravel, in areas near faster currents.
In the Huron River it was found on sand and gravel shoals that had a good current. This species is also found in Lake Erie. (Cummings and Mayer, 1992; van der Schalie, 1938; Watters, 1995)
The rainbow is up to 7.6 cm (3 inches) long , and is elongate and oblong in shape. The shell is usually fairly thin. Males are compressed and females are inflated. The
anterior end is uniformly rounded, the posterior end sharply rounded in females to bluntly pointed in males. The dorsal margin is straight and the ventral margin is straight to gently curved.
Umbos are low, even, or raised slightly above the hinge line. The beak sculpture has four to six double-looped ridges, the first two or three concentric. The umbos also have tubercles at the posterior end.
The periostracum (outer shell layer) is smooth except for growth lines. The shell is yellow to yellow-green with heavy broken green rays. The rays are more numerous on the posterior two-thirds of the shell.
On the inner shell, the
left valve has two
pseudocardinal teeth, which are small, erect, and divergent and sharp-pointed. The two lateral teeth are straight, short and fine. The right valve has one erect, columnar pseudocardinal tooth. Anterior to this tooth sometimes is a smaller nacreous swelling. The one lateral tooth has short and thin.
The beak cavity is shallow. The nacre is bluish-white, more blue posteriorly, and beak cavity is cream-colored. The posterior end is iridescent.
In Michigan, the rainbow can be confused with the ellipse and the rayed bean. The rays on the ellipse are fine, wavy and generally unbroken. The rainbow also has a longer hinge line and has finer teeth. The rayed bean is smaller and generally darker in color and more inflated. (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.
Villosa iris is a long-term brooder. In the Huron River in Michigan, it was gravid from mid-August to the following mid-July. It probably spawns from late July to mid-August 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. Often they are found buried under the substrate. (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. Mantle flaps in the lampsilines are modified to attract potential fish hosts. The rainbow mussel has a mantle flap resembling an aquatic insect. If the mussel recognizes a specific 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. (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 lab trials, Villosa iris glochidia metamorphosed on the green sunfish, smallmouth bass, largemouth bass, Suwanee bass, spotted bass, striped shiner, streamline chub, mosquitofish, greenside darter, rainbow darter, bluebreast darter, blackside darter, and yellow perch. (Neves, et al., 1985; Watters and O'Dee, 1997; Zale and Neves, 1982)
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.
Villosa iris is listed as Endangered in Illinois and Wisconsin. In Michigan and North Carolina it is considered Special Concern. (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.
Neves, R., L. Weaver, A. Zale. 1985. An evaluation of host fish suitability for glochidia of Villosa vanuxemi and V. nebulosa (Pelecypoda: Unionidae). America Midland Naturalist, 113: 13-19.
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. 1997. Potential hosts for Villosa iris (Lea, 1829). Triannual unionid report, 12: 7. Accessed October 01, 2005 at http://ellipse.inhs.uiuc.edu/FMCS/TUR/TUR12.html#p9.
Zale, A., R. Neves. 1982. Fish hosts of four species of lampsiline mussels (Mollusca: Unionidae) in Big Moccasin Creek, Virginia. Canadian Journal of Zoology, 60: 2535-2542.
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.