Sebastes serranoidesRockfish

Ge­o­graphic Range

Olive rock­fish are typ­i­cally found in the Pa­cific Ocean off the coast of Cal­i­for­nia from Del Norte County to Baja Cal­i­for­nia, Mex­ico and is usu­ally found around a depth of 5-100 m (Love and West­phal, 1981). These rock­fish are com­monly called “long-term res­i­dents”, in­di­cat­ing that mi­gra­tion is not com­mon in this species de­spite changes in water con­di­tions. (Green, Green­ley and Starr, 2014). (Green, et al., 2014; Love and West­phal, 1981)

Habi­tat

Ju­ve­nile olive rock­fish are pelagic fish, oc­cu­py­ing a depth less than 100 m. They live close to the shore in rock reefs and kelp forests (Green, Green­ley, and Starr, 2014). After a few months, how­ever, they are found at vary­ing depths (Love and West­phal, 1981). (Green, et al., 2014; Love and West­phal, 1981)

  • Range depth
    5 to 100 m
    16.40 to 328.08 ft

Phys­i­cal De­scrip­tion

Se­bastes ser­ra­noides is gray in color and darker dor­sally. There may be vis­i­ble white spots along the sides, and the fins may have a yel­low tint with a dusky edge. Olive rock­fish have large scales that get smaller to­wards the head. The head is com­pressed and has a long, pointed snout with a lower pro­trud­ing jaw (Eigen­mann and Eigen­mann, 1890). The ju­ve­niles tend to be a lighter brown than the adults and have ir­reg­u­lar spots above the lat­eral line. They may also have small black spots vis­i­ble on the anal fins and a large black spot be­tween dor­sal spines 8 and 11. This large spot is typ­i­cally ab­sent in adult rock­fish larger than 35 cm (Love, 1978). The males usu­ally have larger eyes and longer pec­toral fin. Fe­males tend to grow larger than the males (Love, Yoklavich, and Thorstein­son, 2002). (Eigen­mann and Eigen­mann, 1890; Love, 1978; Love, et al., 2002)

  • Sexual Dimorphism
  • female larger

De­vel­op­ment

Mem­bers of the Se­bastes genus are known to have in­ter­nal fer­til­iza­tion and are ovo­vi­vip­a­rous fishes. The eggs are car­ried and hatch in­side of the ovaries of the fe­male (Hal­dor­son and Love, 1991; Love and Caselle, 1998). The lar­vae of S. ser­ra­noides are re­leased from De­cem­ber through March, the ma­jor­ity of which are re­leased in Jan­u­ary (Love and West­phal, 1981). When the lar­vae are re­leased, they stay in the upper layer of the water. After a month, the lar­vae be­come pelagic ju­ve­niles (Love and Caselle, 1998). After a pe­riod of about 3 to 6 months, these fish begin to set­tle in wa­ters of var­i­ous depths, par­tic­u­larly in rocky reefs and kelp habi­tats (Love and West­phal, 1981). (Hal­dor­son and Love, 1991; Love and Caselle, 1998; Love and West­phal, 1981)

Re­pro­duc­tion

Not much is known about the mat­ing be­hav­iors of olive rock­fish, but it is spec­u­lated that there are sev­eral mech­a­nisms in place to pre­vent cross-breed­ing be­tween closely re­lated species of Se­bastes that have the same mat­ing sea­son. The male cop­u­la­tory or­gans of the olive rock­fish are small mak­ing it dif­fi­cult for other species to fer­til­ize the fe­males of S. ser­ra­noides. There may also be au­di­tory, vi­sual, and chem­i­cal mech­a­nisms at work that pre­vent cross-breed­ing (Love and West­phal, 1981). (Love and West­phal, 1981)

Not much is known about the re­pro­duc­tive gen­eral be­hav­iors of the olive rock­fish; how­ever, the mat­ing sea­son of S. ser­ra­noides is be­lieved to be from Oc­to­ber to De­cem­ber, peak­ing in No­vem­ber (Love, 1978). (Love, 1978)

  • Breeding season
    October to December, peaking in November

Not much is known about the amount of parental in­vest­ment of the olive rock­fish after birth; how­ever, Se­bastes ser­ra­noides is an ovo­vi­vip­a­rous, tak­ing care of the eggs until they are ready to be hatched (Hal­dor­son and Love, 1991; Love and Caselle, 1998). (Hal­dor­son and Love, 1991; Love and Caselle, 1998)

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

Lifes­pan/Longevity

Rock­fish are known to be slow-grow­ing (Hal­dor­son and Love, 1991) with a life span of around 30-50 years (Green, Green­ley, and Starr, 2014). (Green, et al., 2014; Hal­dor­son and Love, 1991)

Be­hav­ior

Olive rock­fish are known to be rel­a­tively sta­ble and are likely to stay in one area de­spite changes in water con­di­tions. They are also more ac­tive dur­ing the day than at night (Green, Green­ley, and Starr, 2014). At around 1 to 4 inches, ju­ve­niles are typ­i­cally found in schools, but as they grow larger, they tend to pre­fer soli­tude (Lim­baugh, 1955). (Green, et al., 2014; Lim­baugh, 1955)

Home Range

Se­bastes ser­ra­noides are typ­i­cally found off the coast of Cal­i­for­nia from Del Norte County to Baja Cal­i­for­nia, Mex­ico.

Com­mu­ni­ca­tion and Per­cep­tion

Not much is known about com­mu­ni­ca­tion of olive rock­fish, but it is sus­pected that there are au­di­tory, vi­sual, and chem­i­cal mech­a­nisms used by the fish in order to pre­vent cross-breed­ing be­tween closely re­lated species (Love and West­phal, 1981). (Love and West­phal, 1981)

Food Habits

The food habits of the olive rock­fish change as the fish gets older and de­pend­ing on the sea­son. Ju­ve­nile rock­fish are de­pen­dent on plank­ton and small fishes found in mid­wa­ters as a source of food. Dur­ing the up­welling pe­riod, the rock­fish de­pends more on nek­ton, such as squid and young rock­fish. The de­pen­dence on young rock­fish, how­ever, de­creases in the fall and win­ter due to the ju­ve­niles be­com­ing older and are un­able to be eas­ily caught. Dur­ing these sea­sons, other prey are tar­geted, such as the north­ern an­chovy. The diet of adult rock­fish mainly con­sists of small fishes, such as blue rock­fish, young olive rock­fish, and pipefish, and of sub­strate-ori­ented prey, such as oc­to­pus and squid (Love & West­phal, 1981). (Love and West­phal, 1981)

  • Animal Foods
  • fish
  • mollusks
  • aquatic crustaceans

Pre­da­tion

Dur­ing the up­welling pe­riod, ju­ve­nile olive rock­fish, as well as other species of rock­fish, are an im­por­tant food source for adult rock­fish and other fish species (Love and West­phal, 1981). Not much is known about what or­gan­isms prey on the adults of this species. (Love and West­phal, 1981)

Ecosys­tem Roles

Ju­ve­nile rock­fish are an im­por­tant food source for other adult rock­fish and other species of fish. The adults of this species feed on small fishes and on sub­strate-ori­ented prey, such as oc­to­pus and squid (Love and West­phal, 1981). Pre­da­tion is im­por­tant for the reg­u­la­tion of the pop­u­la­tion sizes of these food sources (John­son, 2006). The olive rock­fish were thought to be re­plac­ing the kelp bass in the areas around cen­tral and north­ern Cal­i­for­nia (Lim­baugh, 1955), but this is un­likely since the two fish species do not typ­i­cally rely on the same food sources (Love and West­phal, 1981). (John­son, 2006; Lim­baugh, 1955; Love and West­phal, 1981)

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Olive rock­fish are im­por­tant both as a sports fish and in the com­mer­cial fish­ing in­dus­try (Schroeder and Love, 2002; O’Far­rell and Bots­ford, 2006; Love et al., 1990). (Love, et al., 1990; O'Far­rell and Bots­ford, 2006; Schroeder and Love, 2002)

  • Positive Impacts
  • food

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

Not much is known about the olive rock­fish's neg­a­tive im­pacts on hu­mans.

Con­ser­va­tion Sta­tus

The olive rock­fish is not a threat­ened species; how­ever, there is ev­i­dence that the pop­u­la­tion of rock­fish found off the coast of south­ern Cal­i­for­nia has de­clined. There was a sharp drop in the pop­u­la­tion dur­ing the 1970s, and the pop­u­la­tion has re­mained at a con­stant low level pos­si­bly due to en­vi­ron­men­tal con­di­tions and over­fish­ing (Love and Caselle, 1998). (Love and Caselle, 1998)

Con­trib­u­tors

Thanh-Van Nguyen (au­thor), Louisiana State Uni­ver­sity, Prosanta Chakrabarty (ed­i­tor), Louisiana State Uni­ver­sity, Tanya Dewey (ed­i­tor), Uni­ver­sity of Michi­gan-Ann Arbor.

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

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

chemical

uses smells or other chemicals to communicate

coastal

the nearshore aquatic habitats near a coast, or shoreline.

diurnal
  1. active during the day, 2. lasting for one day.
fertilization

union of egg and spermatozoan

food

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

internal fertilization

fertilization takes place within the female's body

molluscivore

eats mollusks, members of Phylum Mollusca

motile

having the capacity to move from one place to another.

natatorial

specialized for swimming

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.

pelagic

An aquatic biome consisting of the open ocean, far from land, does not include sea bottom (benthic zone).

piscivore

an animal that mainly eats fish

planktivore

an animal that mainly eats plankton

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

sexual

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

solitary

lives alone

tactile

uses touch to communicate

visual

uses sight to communicate

Ref­er­ences

Eigen­mann, C., R. Eigen­mann. 1890. De­scrip­tion of a new species of Se­bas­todes. Pro­ceed­ings of the Cal­i­for­nia Acad­emy of Sci­ences, 3: 36-38.

Green, K., A. Green­ley, R. Starr. 2014. Move­ments of blue rock­fish (Se­bastes mysti­nus) off cen­tral Cal­i­for­nia with com­par­isons to sim­i­lar species. Plos One, 9: 1-11.

Hal­dor­son, L., M. Love. 1991. Ma­tu­rity and fe­cun­dity in the rock­fishes, Se­bastes spp., a re­view. Ma­rine Fish­eries Re­view, 53: 25-31.

John­son, D. 2006. Pre­da­tion, habi­tat com­plex­ity, and vari­a­tion in den­sity-de­pen­dent mor­tal­ity of tem­per­ate reef fishes. Ecol­ogy, 87: 1179-1188.

Lim­baugh, C. 1955. "Fish life in the kelp beds and the ef­fects of kelp har­vest­ing" (On-line pdf). Ac­cessed No­vem­ber 01, 2015 at http://​escholarship.​org/​uc/​item/​4w36x6mb.

Love, M., J. Caselle. 1998. De­clines in nearshore rock­fish re­cruit­ment and pop­u­la­tions in the south­ern Cal­i­for­nia Bight as mea­sured by im­pinge­ment rates in coastal elec­tri­cal power gen­er­at­ing sta­tions. Fish­ery Bul­letin, 96: 492-501.

Love, M., P. Mor­ris, M. Mc­Crae, R. Collins. 1990. Life his­tory as­pects of 19 rock­fish species (Scor­paenidae: Se­bastes) from the south­ern Cal­i­for­nia Bight. NOAA Tech­ni­cal Re­port NMFS, 87: 1-38.

Love, M., W. West­phal. 1981. Growth, re­pro­duc­tion, and food habits of olive rock­fish, Se­bastes ser­raoides, off cen­tral Cal­i­for­nia. Fish­ery Bul­letin, 79: 533-545.

Love, M., M. Yoklavich, L. Thorstein­son. 2002. The rock­fishes of the north­east Pa­cific. Berke­ley, CA: Uni­ver­sity of Cal­i­for­nia Press.

Love, M. 1978. "As­pects of the life his­tory of the olive rock­fish, Se­bastes ser­ra­noides" (On-line pdf). Ac­cessed Oc­to­ber 06, 2015 at https://​escholarship.​org/​uc/​item/​26j8768b.

O'Far­rell, M., L. Bots­ford. 2006. Es­ti­mat­ing the sta­tus of nearshore rochfk­ish (Se­bastes spp.) pop­u­la­tions with length fre­quency data. Eco­log­i­cal Ap­pli­ca­tions, 16: 977-986.

Schroeder, D., M. Love. 2002. Recre­ational fish­ing and ma­rine fish pop­u­la­tions in Cal­i­fo­nia. Cal­i­for­nia Co­op­er­a­tive Oceanic Fish­eries In­ves­ti­ga­tions Re­port, 43: 182-190.