Chlamydoconcha orcutti

Ge­o­graphic Range

Chlamy­do­con­cha or­cutti is found along the west coast of North Amer­ica (East­ern Pa­cific), from north­ern Cal­i­for­nia (Shell Beach, Sonoma Co. (38.4°N)), south to Punta San Pablo, Baja Cal­i­for­nia Sur (27.2°N). (Carl­ton, 1979; Coan, et al., 2000)

Habi­tat

This species oc­curs near shore, from the in­ter­tidal zone to 40m depth. It was nor­mally found under rocks, crawl­ing or an­chored by byssal threads. Some­times it can also be found within kelp hold­fasts. (Carl­ton, 1979; Coan, et al., 2000)

  • Range depth
    0 to 40 m
    0.00 to 131.23 ft

Phys­i­cal De­scrip­tion

Chlamy­do­con­cha or­cutti is one of the most pe­cu­liar look­ing clams, com­monly known as the “naked clam”. In large adults (see re­pro­duc­tion sec­tion for more in­for­ma­tion about dwarf males) the shells are highly re­duced and com­pletely em­bed­ded in the en­larged, translu­cent white man­tle. The shells grow mostly an­te­ri­orly and have lit­tle pos­te­rior growth, re­sult­ing in an elon­gated, lance­o­late shape. The prodis­so­conch (rudi­men­tary lar­val shell) is often clearly de­mar­cated. (Mor­ton, 1981)

The man­tle is greatly thick­ened and fused, form­ing an “en­ve­lope” that en­closes the shells. The an­te­rior man­tle open­ing acts as the in­halant path­way for the an­i­mal and a pos­te­rior siphon forms the ex­ha­lent open­ing. The dor­sal-lat­eral sur­face of the man­tle ex­hibits many white papil­lae that are re­tractable into pits. The papil­lae have var­i­ous spher­i­cal in­clu­sions that act as se­cre­tory tubules. Those papil­lae may have a chem­i­cal de­fense func­tion pro­tect­ing the an­i­mal from its preda­tors. A group of unique papil­lae also ex­ists be­hind the an­te­rior man­tle open­ing, form­ing an anemone-like disc struc­ture known as the pheromone organ. (Mor­ton, 1981; Rouse, 2011)

Chlamy­do­con­cha or­cutti has a very large and mus­cu­lar foot that en­ables it to crawl around very ac­tively; to­gether with the thick­ened man­tle, they give this an­i­mal an ap­pear­ance of a sea slug rather than a clam. Rouse, 2011 is a video of two live spec­i­mens in cap­tiv­ity– have a look for your­self! (Rouse, 2011)

  • Sexual Dimorphism
  • female larger
  • sexes shaped differently
  • Range length
    4 to 13.5 mm
    0.16 to 0.53 in

De­vel­op­ment

The fer­til­ized eggs are brooded in man­tle cav­i­ties of fe­males, then re­leased as veliger lar­vae. No de­tailed stud­ies have been done on the de­vel­op­ment of this species. How­ever, stud­ies on species from the same su­per­fam­ily show that early cleav­age to lar­val re­lease may take 12-29 days, or even up to 2 months. The veligers feed on the plank­ton and meta­mor­pho­sis into ju­ve­niles. (Jes­persen and Lützen, 2006)

Re­pro­duc­tion

Chlamy­do­con­cha or­cutti has two very dif­fer­ent adult body forms. Large in­di­vid­u­als as de­scribed above are typ­i­cally her­maph­ro­ditic. They pos­sess both fe­male and male re­pro­duc­tive or­gans and both can be func­tional, al­though some­times one sex may be much more de­vel­oped than the other. How­ever, tiny sex­u­ally ma­ture “dwarf” males are often pre­sent. They are sig­nif­i­cantly smaller than the large her­maph­ro­ditic adults and can­not live by them­selves. Dwarf males are typ­i­cally found in­side man­tle cav­i­ties of large in­di­vid­u­als, at­tached by byssal threads. Their shells have promi­nent prodis­so­conchs and are also cov­ered with ex­tended man­tle tis­sue. (Mor­ton, 1981)

Chlamy­do­con­cha or­cutti is a protan­dric se­quen­tial her­maph­ro­dite. In the pres­ence of large con­specifics, plank­tonic larva may meta­mor­phose di­rectly into dwarf male forms, but this is not a per­ma­nent stage. If en­vi­ron­men­tal con­di­tions allow, dwarf males can sub­se­quently de­velop into large her­maph­ro­ditic body form. The evol­lu­tion of dwarf male morphs may rep­re­sent adap­ta­tion to small pop­u­la­tion sizes and iso­lated dis­tri­b­u­tions. (Mor­ton, 1981; Ó Foighil, 1985)

Dwarf males or her­maph­ro­ditic large adults re­lease sper­ma­to­zoa that are taken up by the in­cur­rent siphon of the egg-pro­duc­ing part­ner. The eggs are fer­til­ized and in­cu­bated in the suprabranchial cham­ber of the fe­male/her­maph­ro­dite. (Mor­ton, 1981)

Chlamy­do­con­cha or­cutti are brood­ers, i.e., fer­til­ized eggs and de­vel­op­ing em­bryos are pro­tected in­side the man­tle cav­ity until they are re­leased as free-liv­ing plank­tonic lar­vae. (Mor­ton, 1981)

  • Parental Investment
  • pre-hatching/birth
    • protecting
      • female

Lifes­pan/Longevity

Most Chlamy­do­con­cha or­cutti adult in­di­vid­u­als were ob­served in fall and win­ter (Au­gust to Jan­u­ary, oc­ca­sion­ally in April), with pop­u­la­tion peaks about Oc­to­ber. Lifes­pan of this species is not de­ter­mined, but the clam could prob­a­bly live for sev­eral years. (Carl­ton, 1979; Mor­ton, 1981)

Be­hav­ior

Chlamy­do­con­cha or­cutti nor­mally at­taches to the bot­tom of rocks, how­ever when de­tached, it can crawl and move ac­tively with it's large, mus­cu­lar foot. (Mor­ton, 1981)

Com­mu­ni­ca­tion and Per­cep­tion

The pheromone organ de­scribed above is sug­gested to be se­cre­tory and might be used to at­tract and guide males. (Bernard, 1897; Mor­ton, 1981)

Food Habits

Chlamy­do­con­cha or­cutti is a sus­pen­sion feeder, it gath­ers food par­ti­cles from the water col­umn by pass­ing cur­rent through its cteni­dia (“gills”). Fil­tered ma­te­r­ial trav­els within food grooves to the mouth. (Mor­ton, 1981)

Pre­da­tion

Spe­cific preda­tors of Chlamy­do­con­cha or­cutti are not iden­ti­fied, but it could be po­ten­tially be pre­dated by a spec­trum of ben­thic preda­tors if they can have ac­cess to it. Chlamy­do­con­cha or­cutti nor­mally hides under rocks; papil­lae on the man­tle of the clam are likely to be chem­i­cal de­fen­sive or­gans that pro­tect the an­i­mal from its preda­tors. (Mor­ton, 1981)

Ecosys­tem Roles

Very lit­tle is known about the ecol­ogy of this species, or its eco­log­i­cal re­la­tion­ships with other species.

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

There are no known pos­i­tive ef­fects of Chlamy­do­con­cha or­cutti on hu­mans.

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

There are no known ad­verse ef­fects of Chlamy­do­con­cha or­cutti on hu­mans.

Con­ser­va­tion Sta­tus

Very lit­tle is known about the pop­u­la­tion sta­tus of this species. It does not re­ceive any spe­cial legal pro­tec­tion.

Con­trib­u­tors

Jingchun Li (au­thor), Spe­cial Pro­jects, George Ham­mond (ed­i­tor), An­i­mal Di­ver­sity Web Staff.

Glossary

Pacific Ocean

body of water between the southern ocean (above 60 degrees south latitude), Australia, Asia, and the western hemisphere. This is the world's largest ocean, covering about 28% of the world's surface.

World Map

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.

chemical

uses smells or other chemicals to communicate

coastal

the nearshore aquatic habitats near a coast, or shoreline.

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.

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.

internal fertilization

fertilization takes place within the female's body

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.

ovoviviparous

reproduction in which eggs develop within the maternal body without additional nourishment from the parent and hatch within the parent or immediately after laying.

pheromones

chemicals released into air or water that are detected by and responded to by other animals of the same species

planktivore

an animal that mainly eats plankton

protandrous

condition of hermaphroditic animals (and plants) in which the male organs and their products appear before the female organs and their products

saltwater or marine

mainly lives in oceans, seas, or other bodies of salt water.

sedentary

remains in the same area

sexual

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

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

Bernard, F. 1897. Note prélim­i­naire sur Chlamy­do­con­cha Or­cutti Dall, Lamel­li­branche à co­quille in­terne. Bul­letin du Muséum d'His­toire Na­turelle, 3: 65-67.

Carl­ton, J. 1979. Chlamy­do­con­cha or­cutti Dall: re­view and dis­tri­b­u­tion of a lit­tle-known bi­valve. Veliger, 21: 375-378.

Coan, E., P. Valen­tich-Scott, F. Bernard. 2000. Bi­valve Seashells of West­ern North Amer­ica. Santa Bar­bara: Santa Bar­bara Musuem.

Jes­persen, Å., J. Lützen. 2006. Re­pro­duc­tion and sperm struc­ture in Ga­le­om­mati­dae (Bi­valvia, Ga­le­om­ma­toidea). Zoomor­phol­ogy, 125: 157-173.

Mor­ton, B. 1981. The bi­ol­ogy and func­tional mor­phol­ogy of Chlamy­do­con­cha or­cutti with a dis­cus­sion on the tax­o­nomic sta­tus of the Chlamy­do­con­chacea (Mol­lusca: Bi­valvia). Jour­nal of Zo­ol­ogy, Lon­don, 195: 81–121.

Rouse, G. 2011. "Chlamy­do­con­cha" (On-line). Ac­cessed Au­gust 19, 2011 at http://​www.​youtube.​com/​watch?​v=Kr7m_​OSzwV8.

Ó Foighil, D. 1985. Form, func­tion and ori­gin of tem­po­rary dwarf males in Pseudopy­thina rugifera (Car­pen­ter, 1864) (Bi­valvia: Ga­le­om­mat­acea). Veliger, 27: 245–252.