Dreissena bugensis

Ge­o­graphic Range

Orig­i­nally, Dreis­sena bu­gen­sis had a re­stricted dis­tri­b­u­tion. Quagga mus­sels were lo­cated in the Dnieper-Bug Es­tu­ary and In­guletz river in Ukraine where they were first dis­cov­ered in 1890. They began to ex­pand through­out East­ern Eu­rope into the Black Sea, Dnieper River, Prip­iat River, Main and Rhine Rivers, and to the Don and Manych Rivers. Then, 40 years after the open­ing of the Volga-Don canal, they in­vaded the Volgo-Caspian. The canal con­nected the two. They have also spread to North Amer­ica and Canada, in Lake On­tario in 1991. The quagga mus­sel has spread through­out the Great Lakes and the Mis­sis­sippi River, into Michi­gan, Mis­souri, New York, Nevada, Ohio, Penn­syl­va­nia, Col­orado, Ari­zona and Cal­i­for­nia. (Mills, et al., 1996; Rin­te­len and Van Damme, 2014)

Habi­tat

Quagga mus­sels live in fresh­wa­ter es­tu­ar­ine habi­tats. Dur­ing the plank­tonic stage the larva swims as a free-liv­ing crea­ture in the water. When the mus­sels be­come ju­ve­niles they at­tach to nat­ural hard sur­faces such as rocks, wood, and plants na­tive to the fresh­wa­ter lake or pond. In deeper wa­ters where there is less tur­bu­lence, they are also able to col­o­nize soft sur­faces such as sand. These mus­sels also at­tach them­selves to man-made struc­tures made of steel, wood, nylon, metal pip­ing, or con­crete. Ma­ture mus­sels tend to at­tach them­selves to these sur­face struc­tures right under the sur­face of the water less than 100 me­ters down un­less the wind ag­i­tates them, in which case they will live a lit­tle deeper down. They have been found as deep as 140 m, though most are found at a depth of about 4 to 10 m. (Brit­ton, 2007; Ian­niello, 2013; Mills, et al., 1996; Ussery and McMa­hon, 1995)

  • Aquatic Biomes
  • lakes and ponds
  • rivers and streams
  • Range depth
    140 (high) m
    459.32 (high) ft

Phys­i­cal De­scrip­tion

Dreis­sena bu­gen­sis, also known as the quagga mus­sel is a fresh­wa­ter bi­valve mol­lusk. Dur­ing the lar­val, or veliger stage the quagga mus­sel is mi­cro­scopic at a size rang­ing from 40 to 462 mi­crom­e­ters. A full grown quagga mus­sel is no larger than a thumb­nail, which is about 30 to 40 mil­lime­ters. The shell of the mus­sel is a light brown to al­most white by the hinge of the shell with black or dark brown stripes/rings. The shell is fan-shaped with edges that come to points on both sides. Be­tween the ven­tral and dor­sal sides the shell has a very rounded angle, or ca­rina. The ven­tral side of the shell is con­vex, mak­ing it im­pos­si­ble for the shell to be able to stand up. When quag­gas are looked at from the ven­tral view it is very clear that the two valves of the mus­sel are asym­met­ri­cal. (Ben­son, et al., 2013; Sykes, 2010; "Quagga Mus­sels", 2014)

  • Range length
    30 to 40 mm
    1.18 to 1.57 in

De­vel­op­ment

The life cycle of the quagga mus­sel starts when fer­til­iza­tion is done ex­ter­nally in the water. Sev­eral days after fer­til­iza­tion, tro­chophore larva de­velop, start­ing the plank­tonic stage of de­vel­op­ment. A tro­chophore is a free-swim­ming larva. In 4 to 5 days the tro­chophore will change into a D-shaped veliger. Soon the larva will form a part of its shell called the um­bone mak­ing the larva known as an um­bonal veliger. Then the veliger will de­velop a foot shaped struc­ture, a char­ac­ter­is­tic of all mol­lusks, be­com­ing a pe­di­veliger. With the for­ma­tion of the shell and foot the pe­di­veliger is now able to at­tach it­self to a sub­strate and start de­vel­op­ing into a ju­ve­nile mus­sel. Quagga mus­sels often stay in the form of a veliger for sev­eral weeks be­fore start­ing the process of be­com­ing a ma­ture mus­sel. Once a veliger be­comes a ju­ve­nile mus­sel it has en­tered into the ben­thic stage of de­vel­op­ment where it be­comes ses­sile and be­gins to grow. When a fe­male set­tles into the ju­ve­nile stage, it can start re­pro­duc­ing on its sec­ond year of life. (Ian­niello, 2013)

Re­pro­duc­tion

Fer­til­iza­tion is ex­ter­nal for Dreis­sena bu­gen­sis, so mat­ing is lim­ited to males and fe­males in prox­im­ity to each other re­leas­ing their ga­metes into the water. (Ian­niello, 2013)

Dreis­sena bu­gen­sis are pro­lific breed­ers and they pro­duce ga­metes in abun­dance. Fe­male dreis­senids can pro­duce 40,000 eggs in one re­pro­duc­tive cycle. Fe­males and males live to­gether and fer­til­iza­tion is ex­ter­nal once the ga­metes are re­leased into the water. Water tem­per­a­ture has an ef­fect on re­pro­duc­tion, as warmer water tem­per­a­tures have shown to ini­ti­ate quagga mus­sel spawn­ing. Typ­i­cally, quagga mus­sels re­pro­duce year round. (Ian­niello, 2013)

  • Breeding season
    Mating takes place year-round.

There is no parental care for Dreis­sena bu­gen­sis. Fer­til­iza­tion oc­curs out­side the body of the fe­male, and the de­vel­op­ing mus­sels are en­tirely in­de­pen­dent of the par­ents. (Ian­niello, 2013)

  • Parental Investment
  • no parental involvement

Lifes­pan/Longevity

Typ­i­cally the lifes­pan of the Dreis­sena bu­gen­sis is 4 to 5 years. (Ian­niello, 2013)

  • Typical lifespan
    Status: wild
    4 to 5 years

Be­hav­ior

Adult quagga mus­sels are ses­sile, mean­ing that they are fixed in one place and im­mov­able. The lar­val stage is free-swim­ming. (Mackie, 2010)

Com­mu­ni­ca­tion and Per­cep­tion

These mol­lusks have no head or eyes. There­fore, they are not able to see. They are able to de­tect chem­i­cals in the water, as well as grav­ity, move­ment, and tem­per­a­ture. If quagga mus­sels feel threat­ened, they will tightly close their shell. (Mackie, 2010)

Food Habits

These mus­sels are fil­ter feed­ers, mean­ing that they fil­ter plank­ton and nu­tri­ents sus­pended in the water. They use cilia, hair-like pro­jec­tions, to pull water into their shell through a tube-like struc­ture, the in­cur­rent siphon. The nu­tri­ents are then fil­tered out and the water then leaves the body of the mus­sel through an­other tube-like struc­ture, the ex­cur­rent siphon. Adult mus­sels are able to fil­ter out about one liter of water each day. Fil­ter­ing can re­move phy­to­plank­ton, zoo­plank­ton, and algae. (Mackie, 2010)

Pre­da­tion

Quagga mus­sels have few nat­ural preda­tors. One preda­tor is yel­low perch, Perca flavescens. A study in 1994 showed that yel­low perch found D. bu­gen­sis un­palat­able, yet ten years later a sec­ond study found that yel­low perch had in­tro­duced the quagga mus­sel into its diet, be­com­ing one of its few nat­ural preda­tors. (Pop­ple, 2006)

Ecosys­tem Roles

As an in­va­sive species, Dreis­sena bu­gen­sis has a sig­nif­i­cant im­pact on the en­vi­ron­ment. Quagga mus­sels can fil­ter large quan­ti­ties of water, de­creas­ing the lev­els of plank­ton and nu­tri­ents in the water, de­priv­ing other or­gan­isms. Quagga mus­sels often co-habi­tate with the closely re­lated zebra mus­sel, Dreis­sena poly­mor­pha, an­other in­va­sive species. Quagga mus­sels have ac­tu­ally dis­placed zebra mus­sels in Ukraine, and ap­pear to be doing so in the Great Lakes as well. Quagga mus­sels are ca­pa­ble of col­o­niz­ing sur­faces at greater depths than zebra mus­sels, so they tend to dom­i­nate at these lower depths.

Quagga mus­sels also have few nat­ural preda­tors, ex­cept for yel­low perch, which al­lows them to fur­ther dom­i­nate wa­ter­ways. The pre­da­tion by yel­low perch may ac­tu­ally be­come detri­men­tal, as a bot­u­lism caus­ing bac­te­ria called Clostrid­ium bot­u­linum that ac­cu­mu­lates in the quagga mus­sels through their feed­ing habits is now being ex­posed to the pre-ex­ist­ing food chain. Clostrid­ium bot­u­linum has al­ready caused heavy dam­age in Lake Erie, killing tens of thou­sands of bird and fish species, pos­ing a se­ri­ous threat to what­ever ecosys­tem it is pre­sent in. (Pop­ple, 2006; Hickie, 2010; Mills, et al., 1996; Pop­ple, 2006)

Com­men­sal/Par­a­sitic Species
  • bac­terium, Clostrid­ium bot­u­linum

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

There are no known pos­i­tive ef­fects of Dreis­sena bu­gen­sis on hu­mans.

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

Dreis­sena bu­gen­sis is a per­sis­tent in­va­sive species, form­ing thick lay­ers on wa­ter­ways, im­ped­ing water flow, even clog­ging pipes in water treat­ment plants. The fil­ter feed­ing abil­i­ties of quagga mus­sels lower plank­ton lev­els and re­lease pseu­do­fe­ces that raise acid lev­els in the water it in­hab­its, caus­ing is­sues for other or­gan­isms in their habi­tat. (Hickie, 2010; Hod­dle, 2011)

Con­ser­va­tion Sta­tus

Dreis­sena bu­gen­sis is cat­e­go­rized as "least con­cern" by the IUCN. As a sig­nif­i­cant in­va­sive species, with a grow­ing pop­u­la­tion, ef­forts are con­cerned with con­trol­ling pop­u­la­tions, rather than con­ser­va­tion. (Mackie, 2010)

Con­trib­u­tors

Ash­ley Eaton (au­thor), Grand View Uni­ver­sity, Cody Red­mond (au­thor), Grand View Uni­ver­sity, LundyS Van­sy­lalom (au­thor), Grand View Uni­ver­sity, Fe­lic­i­tas Aven­dano (ed­i­tor), Grand View Uni­ver­sity, Dan Chib­nall (ed­i­tor), Grand View Uni­ver­sity, An­gela Miner (ed­i­tor), An­i­mal Di­ver­sity Web Staff.

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

acoustic

uses sound to communicate

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

ectothermic

animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature

estuarine

an area where a freshwater river meets the ocean and tidal influences result in fluctuations in salinity.

external fertilization

fertilization takes place outside the female's body

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.

introduced

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

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.

native range

the area in which the animal is naturally found, the region in which it is endemic.

phytoplankton

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

planktivore

an animal that mainly eats plankton

sedentary

remains in the same area

sessile

non-motile; permanently attached at the base.

Attached to substratum and moving little or not at all. Synapomorphy of the Anthozoa

sexual

reproduction that includes combining the genetic contribution of two individuals, a male and a female

tactile

uses touch to communicate

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).

year-round breeding

breeding takes place throughout the year

zooplankton

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

Ref­er­ences

Wis­con­sin DNR. 2014. "Quagga Mus­sels" (On-line). EEK-Crit­ter Cor­ner. Ac­cessed March 01, 2014 at http://​dnr.​wi.​gov/​org/​caer/​ce/​eek/​critter/​invert/​quaggamussel.​htm.

Ben­son, A., M. Rich­er­son, E. May­nard, J. Lar­son, A. Fusaro. 2013. "Dreis­sena ros­tri­formis bu­gen­sis" (On-line). USGS-Non­i­dige­nous Aquatic Species. Ac­cessed March 05, 2014 at http://​nas.​er.​usgs.​gov/​queries/​FactSheet.​aspx?​speciesID=95.

Brit­ton, D. 2007. "Zebra & Quagga Mus­sel In­va­sion in North Amer­ica" (On-line pdf). U.S. Fish & Wildlife Ser­vice. Ac­cessed March 01, 2014 at http://​www.​100thmeridian.​org/​ActionTeams/​RioGrande/​zq.​pdf.

Hickie, V. 2010. "The Quagga Mus­sel Cri­sis At Lake Mead Na­tional Recre­ation Area" (On-line). EBSCO Host. Ac­cessed April 04, 2014 at http://​web.​a.​ebscohost.​com/​ehost/​detail?​sid=39c43653-f8df-4732-8450-f77feab6ad2b%40sessionmgr4005&​vid=1&​hid=4206&​bdata=JnNjb3BlPXNpdGU%3d#​db=aph&​AN=52236531.

Hod­dle, M. 2011. "CISR" (On-line). Quagga & Zebra Mus­sels. Ac­cessed April 02, 2014 at https://​cisr.​ucr.​edu/​quagga_​zebra_​mussels.​html.

Ian­niello, R. 2013. "Ef­fects of En­vi­ron­men­tal Vari­ables on the Re­pro­duc­tion of Quagga Mus­sels (Dreis­sena ros­tri­formis bu­gen­sis) in Lake Mead, NV/AZ" (On-line pdf). UNLV. Ac­cessed March 02, 2014 at http://​digitalscholarship.​unlv.​edu/​cgi/​viewcontent.​cgi?​article=2843&​context=thesesdissertations.

Mackie, G. 2010. "Dreis­sena bu­gen­sis" (On-line). Global In­va­sive Species Data­base. Ac­cessed April 04, 2014 at http://​www.​issg.​org/​database/​species/​ecology.​asp?​si=918&​fr=1&​sts=&​lang=EN.

Mackie, G. 2010. "Dreis­sena bu­gen­sis (mol­lucs)" (On-line). Ac­cessed March 10, 2014 at http://​www.​issg.​org/​database/​species/​ecology.​asp?​si=918&​fr=1&​sts=&​lang=EN.

Mills, E., G. Rosen­berg, A. Spi­dle, M. Ludyan­skiy, Y. Pli­gin, B. May. 1996. A re­view of the bi­ol­ogy and ecol­ogy of the quagga mus­sel (Dreis­sena bu­gen­sis), a sec­ond species of dreis­senid in­tro­duced to North Amer­ica. Amer­i­can Zo­ol­o­gist, 36: 271-286.

Pop­ple, I. 2006. "Perch dis­cover na­ture's junk food" (On-line). Mcgill. Ac­cessed April 04, 2014 at http://​www.​mcgill.​ca/​reporter/​37/​02/​ricciardi/​.

Rin­te­len, T., D. Van Damme. 2014. "Range De­scrip­tion" (On-line). Ac­cessed March 10, 2014 at http://​eol.​org/​data_​objects/​28096977.

Sykes, C. 2010. "De­vel­op­ment of an Ef­fi­cient Method for Re­moval of Quagga Mus­sel Veligers from Trans­port Tanks at Wil­low Beach Na­tional Fish Hatch­ery" (On-line pdf). Ac­cessed March 04, 2014 at http://​www.​lcrmscp.​gov/​reports/​2010/​c30_​quagga_​mussel_​10_​26sep12.​pdf.

Ussery, T., R. McMa­hon. 1995. "Com­par­a­tive Study of the Des­ic­ca­tion Re­sis­tance of Zebra Mus­sels (Dreis­sena poly­mor­pha) and Quagga Mus­sels (Dreis­sena bu­gen­sis)" (On-line pdf). Ac­cessed March 01, 2014 at http://​el.​erdc.​usace.​army.​mil/​elpubs/​pdf/​trel95-6.​pdf.