Margaritifera margaritifera

Ge­o­graphic Range

Mar­gar­i­tifera mar­gar­i­tifera, also known as the fresh­wa­ter pearl mus­sel or the east­ern pearl­shell, is na­tive to Eu­ro­pean rivers and streams. The range stretches from Nor­way to Spain and pop­u­la­tions are found in Great Britain and Scot­land. This species has also been in­tro­duced to North Amer­ica, where siz­able pop­u­la­tions are found in the north­east­ern United States and east­ern Cana­dian coast. ("Na­ture­Serve Ex­plorer: An on­line en­cy­clo­pe­dia of life", 2009; Skin­ner, et al., 2003)

Habi­tat

Fresh­wa­ter pearl mus­sels live buried or partly buried in stream bed sub­strates that have sandy patches sur­rounded by boul­ders and large rocks. They favor rif­fles, com­mon sites for heavy sed­i­men­ta­tion. Areas of fast-flow­ing water low in ni­trates and phos­phates and shaded by ri­par­ian growth are pre­ferred due to the lower like­li­hood of algal blooms. (Moorkens, 2000; Skin­ner, et al., 2003)

Ju­ve­nile fresh­wa­ter pearl mus­sels are more vul­ner­a­ble to fluc­tu­a­tion in en­vi­ron­men­tal con­di­tions than adults and have stricter re­quire­ments for sur­vival as a re­sult. While adults can tem­porar­ily tol­er­ate muddy or silty con­di­tions, ju­ve­niles can­not sur­vive in those habi­tats. They must set­tle in sandy habi­tats in­ter­spersed with rocks and boul­ders. They re­quire clear water not sat­u­rated with small sed­i­ment par­ti­cles that in­ter­fere with their abil­ity to feed. Water that is 0.3 to 0.4 me­ters deep and flow­ing at a rate of 0.25 to 0.75 me­ters per sec­ond is also nec­es­sary for these mus­sels to feed prop­erly. The pH of the water must be under 7.5 in order to sup­port ju­ve­nile pop­u­la­tions. (Hastie, et al., 2000; Skin­ner, et al., 2003)

  • Aquatic Biomes
  • benthic
  • rivers and streams
  • Range depth
    0.3 to 0.4 m
    0.98 to 1.31 ft

Phys­i­cal De­scrip­tion

As bi­valve mol­lusks, fresh­wa­ter pearl mus­sels have hard shells con­sist­ing of two plates at­tached to a hinge. The color and thick­ness of the shell changes over time. Ju­ve­niles have thin shells that are yel­low­ish-brown, whereas adults have thicker shells that are dark, glossy black. All fresh­wa­ter pearl mus­sels, re­gard­less of age, are roughly kid­ney-shaped and have an ap­pendage on the base of their shell called a foot. The foot al­lows them to bur­row into yield­ing ground, move slowly about on sandy soil, and an­chor them­selves in place. They also have a siphon to draw in water, gills to fil­ter out ed­i­ble ma­te­r­ial, and a sec­ond siphon to expel fil­tered water. (Degerman, et al., 2006; Skin­ner, et al., 2003)

Male, fe­male, and her­maph­ro­ditic fresh­wa­ter pearl mus­sels are iden­ti­cal in ap­pear­ance. Dif­fer­ent sexes have the same col­oration and, given equal amounts of food, grow at the same rate. It is there­fore im­pos­si­ble to dis­cover the sex of or­gan­isms with­out dis­sect­ing them.

Fresh­wa­ter pearl mus­sels typ­i­cally grow to 10 to 13 cm in length, al­though there will be a large amount of vari­abil­ity in size in a healthy pop­u­la­tion. A par­tic­u­larly large spec­i­men was over 17 cm long, new­born fresh­wa­ter pearl mus­sels may be smaller than 1 cm long. (Bauer, 1987; Degerman, et al., 2006)

  • Sexual Dimorphism
  • sexes alike
  • Range length
    17.6 (high) cm
    6.93 (high) in
  • Average length
    11.5 cm
    4.53 in

De­vel­op­ment

The zy­gote that forms when sperm and egg meet in­side of the fe­male (or her­maph­ro­dite) mus­sel is called a glochid­ium (plural glochidia). Glochidia spend sev­eral weeks de­vel­op­ing in­side of the mus­sel, even­tu­ally grow­ing 0.6 to 0.7 mm in size and re­sem­bling tiny mus­sels with their shells held open. The glochidia are then re­leased into the open water, where they float with the cur­rent. The next stage of de­vel­op­ment oc­curs on a fish host. If a glochid­ium makes phys­i­cal con­tact with a fish's gills, it will clamp onto the gills and begin de­vel­op­ing into a ju­ve­nile fresh­wa­ter pearl mus­sel. The pres­ence of glochidia in the gills of a fish has no ob­serv­able neg­a­tive ef­fects on the host, but helps the glochidia dis­perse over a wider range than could be pos­si­ble by freely float­ing in a stream. Host at­tach­ments typ­i­cally occur within sev­eral hours of glochidia re­lease. Most glochidia never find a host and die after six days of float­ing in the cur­rent. (Degerman, et al., 2006; Skin­ner, et al., 2003)

Many dif­fer­ent fish can act as hosts to glochidia. In Eu­rope, these fish in­clude huchen (Hucho hucho), At­lantic salmon (Salmo salar), brown trout (Salmo trutta), and Eurasian dace (Phox­i­nus phox­i­nus). Hosts in the United States are pri­mar­ily salmon and trout species, in­clud­ing coho salmon (On­co­rynchus kisutch), rain­bow trout (On­corhynchus mykiss), cutt­throat trout (On­corhynchus clarkii clarkii), chi­nook salmon (On­corhynchus tshawytscha), and sock­eye salmon (On­corhynchus nerka). Brook trout (Salveli­nus fonti­nalis) can also serve as hosts. ("Na­ture­Serve Ex­plorer: An on­line en­cy­clo­pe­dia of life", 2009)

After eight to nine months de­vel­op­ing in a fish's gills, the glochidia de­tach them­selves. This is when young fresh­wa­ter pearl mus­sels are the most vul­ner­a­ble, as there are many fac­tors that could re­sult in death. Should glochidia land in clean gravel or sand sub­strate, they will likely sur­vive and start to grow. But if glochidia land in un­fa­vor­able sub­strates, such as mud or silt, they die. Glochidia are also likely to per­ish if they have not de­vel­oped to a suf­fi­cient size in the host fish. High lev­els of am­mo­nia, ni­trate, phos­phate, sodium, potas­sium, cal­cium, and mag­ne­sium - all of which are chem­i­cals com­monly in­tro­duced to rivers by hu­mans - also have a neg­a­tive im­pact on glochidia sur­vival. For rea­sons not fully un­der­stood, ju­ve­nile mus­sels grow­ing in lo­ca­tions with siz­able aquatic in­sect (Chi­rono­mi­dae) pop­u­la­tions are more likely to sur­vive. If the ju­ve­nile mus­sel sur­vives, its de­vel­op­ment will be slower than an adult's - about one to two mil­lime­ters per year. It will take about twenty years for the ju­ve­nile mus­sel to be­come an adult, at which time it will con­tin­u­ally grow about three mil­lime­ters per year until its death. (Bud­den­siek, 1995; Degerman, et al., 2006; Skin­ner, et al., 2003)

Re­pro­duc­tion

Fresh­wa­ter pearl mus­sels are dioe­cious, mean­ing that fe­males and males exist in the species. Both sexes can also change into her­maph­ro­dites, al­though males rarely do. Her­maph­ro­dites fre­quently can be found in low-den­sity pop­u­la­tions, where there are not enough males to fer­til­ize all of the fe­males. (Bauer, 1987)

In early sum­mer months, cued by ris­ing tem­per­a­tures, males re­lease sperm into the water col­umn, where it is in­gested by fe­males car­ry­ing eggs. There is a draw­back to this sys­tem; since sperm is swept away by the cur­rent, not all fe­males may be­come fer­til­ized in a fresh­wa­ter pearl mus­sel colony. In ad­di­tion, pop­u­la­tions with low num­bers of males may not be able to pro­duce enough sperm to fer­til­ize most of the fe­males. Be­cause of this, mus­sels can un­dergo asex­ual re­pro­duc­tion and self-fer­til­ize as her­maph­ro­dites. For ex­am­ple, fe­males who are po­si­tioned far up­stream of males will not be­come fer­til­ized, and thus may be­come tem­po­rary her­maph­ro­dites. Since her­maph­ro­dites form due to the in­abil­ity of a male to fer­til­ize a fe­male, it is very un­likely for any males to be­come her­maph­ro­dites. (Bauer, 1987)

Sex­ual ma­tu­rity varies with growth rate of the mus­sel, but is typ­i­cally reached in twenty years. The faster the mus­sel can de­velop, the sooner it will be­come sex­u­ally ma­ture. Once they are sex­u­ally ma­ture, fresh­wa­ter pearl mus­sels re­lease sperm or pro­duce eggs every year until they die, al­though only two out of every three fe­males in a typ­i­cal pop­u­la­tion will be fer­tile each year. (Bauer, 1987; Bauer, 1987)

In­ter­est­ingly, fe­cun­dity does not ap­pear to be af­fected by pol­lu­tion, pop­u­la­tion den­sity of mus­sels, or water dis­charge, al­though those fac­tors will cer­tainly af­fect the sur­vival of the off­spring. (Bauer, 1987)

  • Breeding interval
    Sexually mature freshwater pearl mussels breed once every year until their death.
  • Breeding season
    Breeding occurs from June to July.
  • Range number of offspring
    1 to 4000000
  • Range gestation period
    1 to 3 months
  • Range age at sexual or reproductive maturity (female)
    10 to 20 years
  • Average age at sexual or reproductive maturity (female)
    20 years
  • Range age at sexual or reproductive maturity (male)
    10 to 20 years
  • Average age at sexual or reproductive maturity (male)
    20 years

Fer­til­ized eggs spend roughly four weeks de­vel­op­ing in­side the fe­male mus­sel be­fore they are re­leased to the open water. (Degerman, et al., 2006)

  • Parental Investment
  • no parental involvement
  • pre-fertilization
    • provisioning
    • protecting
      • female
  • pre-hatching/birth
    • provisioning
      • female
    • protecting
      • female

Lifes­pan/Longevity

Fresh­wa­ter pearl mus­sels are a long-lived species. The av­er­age lifes­pan ranges from 86 to 102 years, al­though lifes­pan varies greatly with en­vi­ron­men­tal fac­tors such as water qual­ity. The old­est fresh­wa­ter pearl mus­sel was found to be 280 years old. How­ever, few fresh­wa­ter pearl mus­sels sur­vive their first year; most are ei­ther washed away by the cur­rent as glochidia or die due to un­suit­able liv­ing con­di­tions as ju­ve­niles. (Bauer, 1987; Degerman, et al., 2006; Skin­ner, et al., 2003)

  • Range lifespan
    Status: wild
    280 (high) years
  • Average lifespan
    Status: wild
    93 years

Be­hav­ior

Being seden­tary an­i­mals, fresh­wa­ter pearl mus­sels tend to stay in one place and fil­ter food from the water col­umn. Most par­tially bury them­selves in the sand and leave about a third of their shell ex­posed, al­though some com­pletely bury them­selves. If they need to re­lo­cate, fresh­wa­ter pearl mus­sels can use their foot organ to slowly move across sandy sed­i­ments. This foot organ is also the pri­mary means by which adult mus­sels an­chor them­selves to stream beds. Ju­ve­niles, which are con­sid­er­ably smaller than adults and there­fore at greater risk of being swept away by the cur­rent, can also an­chor them­selves to rocks using a thread­like organ called a byssus thread. (Degerman, et al., 2006; Skin­ner, et al., 2003)

Home Range

The home range size of fresh­wa­ter pearl mus­sels is un­known, al­though they typ­i­cally move lit­tle once es­tab­lished at a site.

Food Habits

Fresh­wa­ter pearl mus­sels fil­ter small or­ganic par­ti­cles from the water col­umn. It is not known ex­actly what they eat, but the or­gan­ism's diet likely con­sists of fun­gal spores, bac­te­ria, tiny phy­lo­plank­ton and zoo­plank­ton, and other very small fil­ter­able par­ti­cles. (Degerman, et al., 2006; Skin­ner, et al., 2003)

Algal blooms can in­ter­fere with a fresh­wa­ter pearl mus­sel's abil­ity to fil­ter food from the water. Pop­u­la­tions of zebra mus­sels and other bi­valves can also lead to com­pe­ti­tion for food, as both groups fil­ter for sim­i­lar food ma­te­r­ial. (Degerman, et al., 2006)

Pre­da­tion

Ju­ve­nile fresh­wa­ter pearl mus­sels are eaten by cray­fish, eels, and North Amer­i­can muskrats (On­da­tra zi­bethi­cus). Adult fresh­wa­ter pearl mus­sels do not ap­pear to have any preda­tors. Their thicker shells and larger size pro­tect them from or­gan­isms that typ­i­cally eat ju­ve­niles. (Degerman, et al., 2006)

Ecosys­tem Roles

It has been sug­gested that fresh­wa­ter pearl mus­sels help to keep water clean, al­though their en­vi­ron­men­tal im­pact on water qual­ity is not fully un­der­stood. How­ever, an av­er­age sized adult fresh­wa­ter pearl mus­sel can fil­ter 50 L of water each day, and they also ex­crete waste prod­ucts that are bro­ken down by de­tri­tus-eat­ing or­gan­isms. Those waste prod­ucts con­tain im­por­tant nu­tri­ents for plant life. Fish in gen­eral, par­tic­u­larly fish in the gen­era On­corhynchus and Salmo are im­por­tant hosts for these mus­sels. This com­men­sal re­la­tion­ship does not harm the fish hosts. (Degerman, et al., 2006; Skin­ner, et al., 2003)

Species Used as Host

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

As the name might sug­gest, fresh­wa­ter pearl mus­sels were com­mer­cially im­por­tant in the pearl in­dus­try be­fore they achieved en­dan­gered sta­tus. Il­le­gal har­vest of pearls from pop­u­la­tions of fresh­wa­ter pearl mus­sels con­tinue today, mak­ing it nec­es­sary for wildlife agen­cies to keep se­cret the exact lo­ca­tions of fresh­wa­ter pearl mus­sel pop­u­la­tions. (Skin­ner, et al., 2003)

  • Positive Impacts
  • body parts are source of valuable material

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

There are no ad­verse ef­fects of fresh­wa­ter pearl mus­sels on hu­mans.

Con­ser­va­tion Sta­tus

Fresh­wa­ter pearl mus­sels are listed as an en­dan­gered species and con­ser­va­tion ef­forts have pri­mar­ily been di­rected to­wards in­creas­ing ju­ve­nile pop­u­la­tions. Many pop­u­la­tions con­sist of only adults be­cause en­vi­ron­men­tal con­di­tions are too harsh for ju­ve­niles. Eu­troph­i­ca­tion, where chem­i­cals added into the river cause algal blooms, are par­tic­u­larly dev­as­tat­ing as they in­ter­fere with the fresh­wa­ter pearl mus­sel's abil­ity to ob­tain food, re­pro­duce, and ob­tain oxy­gen from the water. (Moorkens, 2000; Skin­ner, et al., 2003)

An at­tempt to con­serve fresh­wa­ter pearl mus­sels must in­clude an ef­fort to re­store pop­u­la­tions of host fish. In some mus­sel pop­u­la­tions, a lack of host fish for glochidia to at­tach to has led to de­creased num­bers of ju­ve­niles. Causes for the lack of host fishes vary de­pend­ing on the needs of the fish species; com­mon rea­sons in­clude acid­i­fi­ca­tion of lakes and streams and the in­tro­duc­tion of in­va­sive host species that out-com­pete na­tive pop­u­la­tions.

Hu­mans have also im­pacted pop­u­la­tions of fresh­wa­ter pearl mus­sels. Over-har­vest­ing of mus­sels for pearls has di­min­ished many pop­u­la­tions. This prac­tice has been out­lawed in an ef­fort to pro­tect sur­viv­ing pop­u­la­tions, but it con­tin­ues il­le­gally today. (Skin­ner, et al., 2003)

Other Com­ments

Fresh­wa­ter pearl mus­sels have sea­sonal growth bands on their shells. Dif­fer­ences in size be­tween bands can be used as an in­di­ca­tor of the avail­abil­ity of food and the qual­ity of the water in past years.

The fresh­wa­ter pearl mus­sel fam­ily, Mar­gar­i­tiferi­dae is be­lieved, at 200 mil­lion years old, to be the old­est large fresh­wa­ter mus­sel fam­ily in the world. (Degerman, et al., 2006)

Con­trib­u­tors

Daniel Mitchell (au­thor), The Col­lege of New Jer­sey, Keith Pecor (ed­i­tor), The Col­lege of New Jer­sey, Tanya Dewey (ed­i­tor), Uni­ver­sity of Michi­gan-Ann Arbor.

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

Palearctic

living in the northern part of the Old World. In otherwords, Europe and Asia and northern Africa.

World Map

asexual

reproduction that is not sexual; that is, reproduction that does not include recombining the genotypes of two parents

benthic

Referring to an animal that lives on or near the bottom of a body of water. Also an aquatic biome consisting of the ocean bottom below the pelagic and coastal zones. Bottom habitats in the very deepest oceans (below 9000 m) are sometimes referred to as the abyssal zone. see also oceanic vent.

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.

colonial growth

animals that grow in groups of the same species, often refers to animals which are not mobile, such as corals.

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.

indeterminate growth

Animals with indeterminate growth continue to grow throughout their lives.

internal fertilization

fertilization takes place within the female's body

introduced

referring to animal species that have been transported to and established populations in regions outside of their natural range, usually through human action.

iteroparous

offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).

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.

oviparous

reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.

phytoplankton

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

planktivore

an animal that mainly eats plankton

polygynandrous

the kind of polygamy in which a female pairs with several males, each of which also pairs with several different females.

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

solitary

lives alone

temperate

that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).

zooplankton

animal constituent of plankton; mainly small crustaceans and fish larvae. (Compare to phytoplankton.)

Ref­er­ences

Na­ture­Serve. 2009. "Na­ture­Serve Ex­plorer: An on­line en­cy­clo­pe­dia of life" (On-line). Ac­cessed Feb­ru­ary 07, 2010 at http://​www.​natureserve.​org/​explorer/​servlet/​NatureServe?​searchName=Margaritifera+margaritifera.

Bauer, G. 1987. Re­pro­duc­tive Strat­egy of the Fresh­wa­ter Pearl Mus­sel Mar­gar­i­tifera mar­gar­i­tifera. Jour­nal of An­i­mal Ecol­ogy, 56/2: 691-704. Ac­cessed Feb­ru­ary 05, 2010 at http://​www.​jstor.​org/​stable/​5077?​seq=1.

Bud­den­siek, V. 1995. The cul­ture of ju­ve­nile fresh­wa­ter pearl mus­sels Mar­gar­i­tifera mar­gar­i­tifera L. in cages. Bi­o­log­i­cal Con­ser­va­tion, 74: 33-40. Ac­cessed Feb­ru­ary 09, 2010 at http://​www.​sciencedirect.​com/​science?_​ob=ArticleURL&_​udi=B6V5X-4002DR0-R&_​user=1086025&_​coverDate=12%2F31%2F1995&_​rdoc=1&_​fmt=high&_​orig=search&_​sort=d&_​docanchor=&​view=c&_​searchStrId=1200849860&_​rerunOrigin=google&_​acct=C000051441&_​version=1&_​urlVersion=0&_​userid=1086025&​md5=1495d4316e2528bd4b106756d08c6038.

Degerman, E., S. Alexan­der­son, J. Bergen­gren, L. Hen­rik­son, B. Jo­hans­son, B. Larsen, H. Soder­berg. 2006. "Restora­tion of Fresh­wa­ter Pearl Mus­sel Streams" (On-line pdf). Ac­cessed Feb­ru­ary 09, 2010 at http://​www.​wwf.​se/​source.​php/​1257735/​Restoration%20of%20FPM%20streams.​pdf.

Hastie, L., P. Boon, M. Young. 2000. Phys­i­cal mi­cro­hab­i­tat re­quire­ments of fresh­wa­ter pearl mus­sels, Mar­gar­i­tifera mar­gar­i­tifera (L.). Hy­dro­bi­olo­gia, 429: 59-71. Ac­cessed Feb­ru­ary 09, 2010 at http://​www.​springerlink.​com/​content/​h3242rxv00778524/​fulltext.​pdf?​page=1.

Moorkens, E. 2000. Con­ser­va­tion man­age­ment of the fresh­wa­ter pearl mus­sel Mar­gar­i­tifera mar­gar­i­tifera. Irish Wildlife Man­u­als, 9: 1-44. Ac­cessed Feb­ru­ary 03, 2010 at http://​www.​npws.​ie/​en/​media/​Media,4583,en.​pdf.

Skin­ner, A., M. Young, L. Hastie. 2003. Ecol­ogy of the Fresh­wa­ter Pearl Mus­sel. Con­serv­ing Natura 2000 Rivers, 2: 1-20. Ac­cessed Feb­ru­ary 03, 2010 at http://​www.​english-nature.​org.​uk/​lifeinukrivers/​publications/​mussel.​pdf.