Octopus briareus

Ge­o­graphic Range

Caribbean reef oc­to­puses, Oc­to­pus bri­areus, are pre­dom­i­nately found in the Neotrop­i­cal re­gion of the world in warm wa­ters. The range of this species stretches from south­ern Florida in North Amer­ica, through the south­east coast of the Gulf of Mex­ico, the Ba­hamas, and the Caribbean, and con­tin­ues south to the north­ern coast of South Amer­ica. Caribbean reef oc­to­puses have also been known to range into the West In­dies and off the coast of Curaçao. ("Cephalopods of the world: An an­no­tated and il­lus­trated cat­a­logue of cephalo­pod species known to date", 2014)

Habi­tat

Caribbean reef oc­to­puses are pri­mar­ily found in trop­i­cal re­gions, off the coast, in shal­low wa­ters rang­ing from 3-20 me­ters. These oc­to­puses pre­dom­i­nantly in­habit areas with water tem­per­a­tures around 20-30°C. Caribbean reef oc­to­puses are nor­mally found in or around coral reefs, which they use for pro­tec­tion and dens. The dens cho­sen by these oc­topods are usu­ally dark and ex­clude other or­gan­isms. ("Cephalopods of the world: An an­no­tated and il­lus­trated cat­a­logue of cephalo­pod species known to date", 2014; Borer and Lane, 1971; Brunt and Davies, 1994; Jor­dan, 2010)

  • Range depth
    3 to 20 m
    9.84 to 65.62 ft

Phys­i­cal De­scrip­tion

Caribbean reef oc­to­puses are typ­i­cally bright green and blue with red-brown specks across their bod­ies. Chro­matophores, which are spe­cial­ized cells in the skin, allow these oc­to­puses to change col­ors in order to blend in with their back­ground and dis­guise them­selves from preda­tors and prey. These oc­to­puses have siz­able, promi­nent dark red-brown eyes. Their man­tles, the body ex­clud­ing their arms, are an av­er­age of 54 mm long and have been known to grow up to 120 mm. This or­gan­ism, on av­er­age, weighs 1 kg.

At hatch­ing, the young are 15mm, with arms of 7-9mm and a man­tle av­er­ag­ing 5.5 mm. These oc­to­puses emerge with the ap­pear­ance of small adults.

Caribbean reef oc­to­puses have seven rows of teeth. The longest of these oc­to­puses' eight arms, the sec­ond and third, grow, on av­er­age, five times the length of the man­tle. Each arm con­sists of two rows of suck­ers, which are con­nected by loose webs that as­sist in hunt­ing. In males, the right third arm has a hec­to­coty­lus that de­posits sper­matophores, sacks con­tain­ing the sperm for mat­ing. ("Cephalopods of the world: An an­no­tated and il­lus­trated cat­a­logue of cephalo­pod species known to date", 2014; Ka­plan, 1982)

  • Sexual Dimorphism
  • sexes shaped differently
  • Average mass
    1 kg
    2.20 lb
  • Range length
    120 (high) mm
    4.72 (high) in
  • Average length
    54 mm
    2.13 in

De­vel­op­ment

Caribbean reef oc­to­puses hatch roughly 80 days after the eggs are laid. At hatch­ing, they are 15mm, with arms of 7-9mm and a man­tle av­er­ag­ing 5.5 mm. They exit the egg about 15 sec­onds after they first crack it. These oc­to­puses emerge with the ap­pear­ance of small adults. Caribbean reef oc­to­puses grow at a rapid rate, in­creas­ing their weight by 5 per­cent a day. Once oc­to­puses have sex­u­ally ma­tured at five months, they will con­tinue to grow, and ex­hibit in­de­ter­mi­nate growth. By the time they die they will weigh one-third of the amount of food they have eaten over the course of their life. (Sax­ena, 2005; Scheel, et al., 2017)

Re­pro­duc­tion

Oc­to­puses are monog­a­mous, mean­ing one fe­male and male mate. Caribbean reef oc­to­puses do not have a known mat­ing rit­ual. Be­cause oc­to­puses are soli­tary, mates are op­por­tunis­ti­cally cho­sen. Sex­ual re­pro­duc­tion can occur in two dif­fer­ent ways for Caribbean reef oc­to­puses. Males can ei­ther mount the fe­male, reach its hec­to­coty­lus, the sperm con­tain­ing ten­ta­cle, into her oviduct, re­leas­ing its sperm to cover the eggs, or take off its hec­to­coty­lus and give it to the fe­male so that she can store his arm in her man­tle and use it when the eggs are ready to be in­ter­nally fer­til­ized. The males die sev­eral months after fer­til­iz­ing the eggs, while the fe­males die shortly after lay­ing the eggs. (Scheel, et al., 2017)

Oc­to­puses are semel­parous, mean­ing that they only breed once in their life­time be­fore death, and oviparous, which means they are egg lay­ers. Al­though oc­to­puses breed year-round, spawn­ing peaks around Feb­ru­ary-March. Oc­to­puses reach sex­ual ma­tu­rity at five months, but may not re­pro­duce for sev­eral years. Fe­male oc­to­puses can lay up to 200,000 eggs, each of which take ap­prox­i­mately 65 days to hatch. When oc­to­puses hatch, they weigh 0.095g and are 15mm in length on av­er­age. Be­cause both the par­ents are usu­ally de­ceased by the time the eggs hatch, oc­to­puses emerge from their eggs fully in­de­pen­dent. (Aron­son, 1986; Han­lon, 1977; Sax­ena, 2005; Scheel, et al., 2017)

  • Breeding interval
    Octopuses breed once in their lifetime.
  • Breeding season
    Although octopuses breed year-round, spawning peaks around February-March. Most breed between six months to a few years after they reach maturity.
  • Range number of offspring
    200,000 (high)
  • Average gestation period
    65 days
  • Average time to independence
    0 minutes
  • Average age at sexual or reproductive maturity (female)
    5 months
  • Average age at sexual or reproductive maturity (male)
    5 months

Male Caribbean reef oc­to­puses do not have any parental in­volve­ment other than pro­vid­ing sperm to fer­til­ize the eggs. The male oc­to­puses are dead by the time the eggs have hatched. The fe­males pro­tect the eggs pre-fer­til­iza­tion by keep­ing them in­side of their body cav­i­ties. Once the fe­males lay the eggs in crevices, they do not leave them alone, not even to feed. The fe­male oc­to­puses pro­tect the eggs from preda­tors and keep them clean by push­ing water past them. The fe­males usu­ally die be­fore the eggs hatch. (Sax­ena, 2005; Scheel, et al., 2017)

  • Parental Investment
  • female parental care
  • pre-fertilization
    • protecting
      • female
  • pre-hatching/birth
    • protecting
      • female

Lifes­pan/Longevity

Caribbean reef oc­to­puses live 10-12 months, on av­er­age, in the wild. The spo­radic feed­ing habits of these oc­to­puses will de­crease their lifes­pan in the wild. When kept in cap­tiv­ity, these oc­to­puses live 10-17 months on av­er­age. In cap­tiv­ity, their lifes­pan can be de­creased by can­ni­bal­ism, dis­ease, lab­o­ra­tory ac­ci­dents, and es­capes. Male Caribbean reef oc­to­puses die a few months after they give their hec­to­coty­lus to the fe­males for re­pro­duc­tion. The fe­males usu­ally die shortly after lay­ing the eggs and en­sur­ing the eggs are well hid­den to max­i­mize chance of sur­vival. (Han­lon and Forsythe, 1985; Sax­ena, 2005)

  • Average lifespan
    Status: wild
    10-12 months
  • Average lifespan
    Status: captivity
    10-17 months

Be­hav­ior

Caribbean reef oc­to­puses are soli­tary. They live alone in dens along coral reefs, only in­ter­act­ing with oth­ers for mat­ing pur­poses. These oc­to­puses are ter­ri­to­r­ial and de­fend their den, along with the sur­round­ing area, from other oc­to­puses and preda­tors. They can kill other oc­to­puses within their ter­ri­tory and then eat them.

Caribbean reef oc­to­puses are noc­tur­nal, and the night pro­tects them from preda­tors and makes it eas­ier to sneak up on prey.

Oc­to­puses are monog­a­mous, mean­ing one fe­male and male mate. Caribbean reef oc­to­puses do not have a known mat­ing rit­ual. The male ei­ther mounts the fe­male, or take off its hec­to­coty­lus and give it to the fe­male so that she can store it and use the sperm when the eggs are ready to be in­ter­nally fer­til­ized.

Caribbean reef oc­to­puses have many ways to com­mu­ni­cate with other oc­to­puses. These or­gan­isms have a sender-re­ceiver match (a species-spe­cific vo­cal­iza­tion) that al­lows them to com­mu­ni­cate with each other. Oc­to­puses use a com­plex skin dis­play, using the chro­matophores, to form pat­terns that other oc­to­puses are able to com­pre­hend. These oc­to­puses also use their lay­ers of iri­do­cytes deep in the der­mis of their skin, which pro­duce re­flec­tions off the skin, sig­nal­ing to other oc­to­puses. (Aron­son, 1991; Han­lon and Mes­sen­ger, 1996; Igle­sias, et al., 2014; Sny­der­man and Wise­man, 1996)

Home Range

Caribbean reef oc­to­puses are seden­tary. They mainly stay around the same reef, and even the same den, for the ma­jor­ity of their lives. These oc­to­puses are known to only change dens a few times over their life­times. They al­most al­ways re­turn to their dens after hunt­ing. Caribbean reef oc­to­puses change their dens when they are dis­turbed by an in­truder. Home range and ter­ri­tory sizes have not been re­ported in lit­er­a­ture. (Aron­son, 1991; Igle­sias, et al., 2014; Sny­der­man and Wise­man, 1996)

Com­mu­ni­ca­tion and Per­cep­tion

In gen­eral, all oc­to­puses have high-acu­ity-lens eyes on the sides of their heads. This place­ment forces them to use monoc­u­lar vi­sion, which means they only use one eye at a time. They are also color blind, but are able to dis­tin­guish be­tween dif­fer­ent hues and bright­nesses. Oc­to­puses re­spond to sound and use it as a way to find prey. Oc­to­puses have var­i­ous ways of com­mu­ni­cat­ing among them­selves. These or­gan­isms have a sender-re­ceiver match (a species-spe­cific vo­cal­iza­tion) that al­lows them to com­mu­ni­cate with each other. Oc­to­puses use a com­plex skin dis­play, using the chro­matophores, to form pat­terns that other oc­to­puses are able to com­pre­hend. An­other form of com­mu­ni­ca­tion for these species are using their lay­ers of iri­do­cytes in the der­mis of their skin, which pro­duce re­flec­tions off the skin, sig­nal­ing to other oc­to­puses. Oc­to­puses can also change the ap­pear­ance of their skin and their pos­ture, shap­ing their bod­ies into dif­fer­ent pat­terns. These or­gan­isms use their ad­vanced eye­sight and ten­ta­cles, loaded with nerve end­ings, to per­ceive their en­vi­ron­ment. (Bouwma and Her­rnkind, 2010; Byrne, et al., 2002; Shashar and Cronin, 1996)

Food Habits

Caribbean reef oc­to­puses are car­ni­vores. Their pri­mary prey are Caribbean spiny lob­sters (Pan­ulirus argus). These oc­to­puses have also been known to eat other aquatic crus­taceans (i.e., crabs and shrimp), small fish, and small mol­lusks. They are also known to eat other Caribbean reef oc­to­puses, mak­ing the smaller ones vul­ner­a­ble. Caribbean reef oc­to­puses use their seven rows of teeth, suck­ers on their arms, and the web-like struc­tures that con­nect the tops of their arms to­gether to cap­ture and eat prey. These oc­to­puses are known to hur­dle them­selves over reefs, sur­pris­ing their prey, and cap­tur­ing them in their web. Then, the oc­to­puses reach un­der­neath, grab­bing their prey, and guide it to­wards their mouths. They also snatch their prey with an arm and roll it up un­der­neath of them, after which they eat the prey. Less fre­quently, Caribbean reef oc­to­puses have been known to lurk be­hind their prey and grab it with their front arms. Oc­to­puses' food in­take de­pends on the amount of food avail­able, the water tem­per­a­ture (higher tem­per­a­tures favor more food eaten), and whether or not the fe­male is preg­nant (two weeks be­fore lay­ing the eggs, the fe­male re­duces her food in­take by 50 per­cent). ("Sci­en­tists in the Sea", 1972; Borer and Lane, 1971; Borer, 1971; Brunt and Davies, 1994; Han­lon and Mes­sen­ger, 1996)

  • Animal Foods
  • fish
  • mollusks
  • aquatic crustaceans

Pre­da­tion

The known preda­tors of oc­to­puses are sharks, large fish, birds, eels, hu­mans (Homo sapi­ens), other oc­to­puses (feed­ing on smaller in­di­vid­u­als), and some dol­phins and whales. Oc­to­puses have nu­mer­ous anti-preda­tor adap­ta­tions. They have an in­stinct to flee when they feel threat­ened, and they are able to squeeze into smaller spaces, giv­ing them an ad­van­tage over their big­ger preda­tors. Oc­to­puses re­lease ink from a gland which cre­ates a black cloud and al­lows them to es­cape under the dark­ness. Oc­to­puses also are able to change the color of their skin, which is a cryp­tic adap­ta­tion, cam­ou­flag­ing them into their back­ground and hid­ing them from preda­tors. Lastly, oc­to­puses are known to mimic larger an­i­mals by con­fig­ur­ing their bod­ies into dif­fer­ent shapes to scare off preda­tors. (Aron­son, 1991; Sax­ena, 2005; Aron­son, 1991; Sax­ena, 2005)

  • Anti-predator Adaptations
  • mimic
  • cryptic

Ecosys­tem Roles

Caribbean reef oc­to­puses are the hosts for Ag­gre­gata oc­topi­ana, which are par­a­sitic alve­o­lates mainly as­so­ci­ated with in­flam­ma­tion, ul­cer­a­tion, and the de­struc­tion of the host's or­gans, and Di­ge­netic trema­todes. These oc­to­puses are af­fected by ec­topar­a­sitic pro­to­zoans, Ichthy­obodo neca­tor, and meta­zoan par­a­sites in the phy­lum Di­cyemida. Caribbean reef oc­to­puses pri­mar­ily prey on Caribbean spiny lob­sters, Pan­ulirus argus, but are also known to eat aquatic crus­taceans, such as crabs and shrimp, small fish, and small mol­lusks, and other Caribbean reef oc­to­puses. These oc­to­puses are prey for sharks, large fish, birds, eels, hu­mans, Homo sapi­ens, other oc­to­puses, and some dol­phins and whales. (Castel­lanos-Martínez and Gestal, 2013; Gestal, et al., 1999; Glynn and Enochs, 2011; Han­lon and Forsythe, 1985; Han­lon, et al., 1984; Over­street and Hochberg, 1975)

Com­men­sal/Par­a­sitic Species
  • Par­a­sites alve­o­lates (Ag­gre­gata oc­topi­ana)
  • Di­ge­netic trema­todes
  • Ec­topar­a­sitic pro­to­zoans (Ichthy­obodo neca­tor)
  • Meta­zoan par­a­sites (Phy­lum Di­cyemida)

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Caribbean reef oc­to­puses are mainly cap­tured by ar­ti­sanal fish­er­men who end up sell­ing them for pet trade, and, rarely, sold to fish mar­kets for peo­ple to con­sume. These oc­to­puses are used in bio­med­ical re­search, par­tic­u­larly when re­lat­ing the ner­vous sys­tem to be­hav­ior, be­cause of their sim­i­lar be­hav­ior to ver­te­brates. Oc­to­puses have been used to study blood-brain bar­ri­ers, blood pig­ments, im­mune mech­a­nisms, neu­ro­trans­mit­ters, en­vi­ron­men­tal tox­i­col­ogy, and hor­monal con­trol of re­pro­duc­tion and aging. (Han­lon and Forsythe, 1985; Han­lon, 1977)

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

There are no known neg­a­tive eco­nomic im­pacts of Caribbean reef oc­to­puses on hu­mans.

Con­ser­va­tion Sta­tus

Caribbean reef oc­to­puses have not been eval­u­ated by the IUCN Red List. These oc­to­puses have no spe­cial sta­tus on the U.S. Fed­eral List, the State of Michi­gan List, nor the in­ter­na­tional list (CITES). Granted there are no major threats to Caribbean reef oc­to­puses, but minor threats in­clude their har­vest­ing by hu­mans for re­search, food, and pet trade. Ad­di­tional threats in­clude bac­te­r­ial in­fec­tions, Vib­rio para­haemolyti­cus, Vib­rio damsela, and Pseudomonas stutzeri; all cause ul­cers that are com­mon when these oc­to­puses are kept close in cap­tiv­ity. (Han­lon and Forsythe, 1985; Han­lon, 1977)

Con­trib­u­tors

Lind­sey Lee (au­thor), Rad­ford Uni­ver­sity, Alex At­wood (ed­i­tor), Rad­ford Uni­ver­sity, Karen Pow­ers (ed­i­tor), Rad­ford Uni­ver­sity, Joshua Turner (ed­i­tor), Rad­ford Uni­ver­sity, Tanya Dewey (ed­i­tor), Uni­ver­sity of Michi­gan-Ann Arbor.

Glossary

Atlantic Ocean

the body of water between Africa, Europe, the southern ocean (above 60 degrees south latitude), and the western hemisphere. It is the second largest ocean in the world after the Pacific Ocean.

World Map

Neotropical

living in the southern part of the New World. In other words, Central and South America.

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.

carnivore

an animal that mainly eats meat

coastal

the nearshore aquatic habitats near a coast, or shoreline.

cryptic

having markings, coloration, shapes, or other features that cause an animal to be camouflaged in its natural environment; being difficult to see or otherwise detect.

ectothermic

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

female parental care

parental care is carried out by females

fertilization

union of egg and spermatozoan

food

A substance that provides both nutrients and energy to a living thing.

indeterminate growth

Animals with indeterminate growth continue to grow throughout their lives.

internal fertilization

fertilization takes place within the female's body

molluscivore

eats mollusks, members of Phylum Mollusca

monogamous

Having one mate at a time.

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.

nocturnal

active during the night

oviparous

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

pet trade

the business of buying and selling animals for people to keep in their homes as pets.

piscivore

an animal that mainly eats fish

reef

structure produced by the calcium carbonate skeletons of coral polyps (Class Anthozoa). Coral reefs are found in warm, shallow oceans with low nutrient availability. They form the basis for rich communities of other invertebrates, plants, fish, and protists. The polyps live only on the reef surface. Because they depend on symbiotic photosynthetic algae, zooxanthellae, they cannot live where light does not penetrate.

saltwater or marine

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

sedentary

remains in the same area

semelparous

offspring are all produced in a single group (litter, clutch, etc.), after which the parent usually dies. Semelparous organisms often only live through a single season/year (or other periodic change in conditions) but may live for many seasons. In both cases reproduction occurs as a single investment of energy in offspring, with no future chance for investment in reproduction.

sexual

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

solitary

lives alone

sperm-storing

mature spermatozoa are stored by females following copulation. Male sperm storage also occurs, as sperm are retained in the male epididymes (in mammals) for a period that can, in some cases, extend over several weeks or more, but here we use the term to refer only to sperm storage by females.

tactile

uses touch to communicate

territorial

defends an area within the home range, occupied by a single animals or group of animals of the same species and held through overt defense, display, or advertisement

tropical

the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.

visual

uses sight to communicate

Ref­er­ences

Food and Agri­cul­ture Or­ga­ni­za­tion of the United Na­tions. Cephalopods of the world: An an­no­tated and il­lus­trated cat­a­logue of cephalo­pod species known to date. Vol­ume 3, Issue 4. Rome, Italy: Food and Agri­cul­ture Or­ga­ni­za­tion of the United Na­tions. 2014.

U.S. De­part­ment of In­te­rior. Sci­en­tists in the Sea. None. Wash­ing­ton, D.C.: U.S. De­part­ment of In­te­rior. 1972.

Aron­son, R. 1991. Ecol­ogy, pa­le­o­bi­ol­ogy, and evo­lu­tion­ary con­straint in the oc­to­pus. Bul­letin of Ma­rine Sci­ence, 49/1-2: 245-255.

Aron­son, R. 1986. Life his­tory and den ecol­ogy of Oc­to­pus bri­areus Rob­son in a ma­rine lake. Jour­nal of Ex­per­i­men­tal Ma­rine Bi­ol­ogy and Ecol­ogy, 95/1: 37-56.

Berger, D., M. But­ler IV. 2002. Oc­to­puses in­flu­ence den se­lec­tion by ju­ve­nile Caribbean spiny lob­ster. Ma­rine and Fresh­wa­ter Re­search, 52/8: 1049-1053.

Boal, J. 2006. So­cial recog­ni­tion: A top down view of cephalo­pod be­hav­iour. Life and En­vi­ron­ment, 56/2: 69-79.

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Bouwma, P., W. Her­rnkind. 2010. Sound pro­duc­tion in Caribbean spiny lob­ster Pan­ulirus argus and its role in es­cape dur­ing preda­tory at­tack by Oc­to­pus bri­areus. New Zealand Jour­nal of Ma­rine and Fresh­wa­ter Re­search, 43/1: 3-13.

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Cow­den, R., S. Cur­tis. 1973. Ob­ser­va­tions on liv­ing cells dis­so­ci­ated from the organ of Oc­to­pus bri­areus. Ex­per­i­men­tal and Mol­e­c­u­lar Pathol­ogy, 19: 178-185.

Gestal, C., S. Pas­cual, L. Cor­ral, C. Azevedo. 1999. Ul­tra­struc­tural as­pects of the sporo­gony of Ag­gre­gata oc­topi­ana (Api­com­plexa, Ag­gre­gati­dae), a coc­cid­ian par­a­site of Oc­to­pus vul­garis (Mol­lusca, Cephalopoda) from NE At­lantic Coast. Eu­ro­pean Jour­nal of Pro­tis­tol­ogy, 35/4: 417-425.

Glynn, P., I. Enochs. 2011. Coral Reefs: An Ecosys­tem in Tran­si­tion. Dor­drecht, Nether­lands: Springer.

Grober, M. 1988. Re­sponses of trop­i­cal reef fauna to brit­tle-star lu­mi­nes­cence (Echin­o­der­mata: Ophi­uroidea). Jour­nal of Ex­per­i­men­tal Ma­rine Bi­ol­ogy and Ecol­ogy, 115/2: 157-168.

Han­lon, R., J. Mes­sen­ger. 1996. Cephalo­pod Be­hav­iour. Cam­bridge, Great Britain: Cam­bridge Uni­ver­sity Press.

Han­lon, R., M. Wol­ter­d­ing. 1989. Be­hav­ior, body pat­tern­ing, growth and life his­tory of Oc­to­pus bri­areus cul­tured in the lab­o­ra­tory. Amer­i­can Mala­co­log­i­cal Bul­letin, 7/1: 21-46.

Han­lon, R. 1977. Lab­o­ra­tory rear­ing of the At­lantic reef oc­to­pus, Oc­to­pus bri­areus Rob­son, and its po­ten­tial for mar­i­cul­ture. Jour­nal of the World Aqua­cul­ture So­ci­ety, 8: 471-482.

Han­lon, R., J. Forsythe. 1985. Ad­vances in the lab­o­ra­tory cul­ture of oc­to­puses for bio­chem­i­cal re­search. Lab­o­ra­tory An­i­mal Sci­ence, 35/1: 33-40.

Han­lon, R., J. Forsythe, K. Cooper, A. Din­uzzo, D. Folse, M. Kelly. 1984. Fatal pen­e­trat­ing skin ul­cers in lab­o­ra­tory-reared oc­to­puses. Jour­nal of In­ver­te­brate Pathol­ogy, 44/1: 67-83.

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