Shortfin corvinas are demersal, living and feeding near the sandy or gravelly bottoms of shallow coastal (inshore) waters, although they can be found at depths up to 100 meters. Individuals found north of Point Banda, Mexico are most common in protected bays and estuaries and is also found in mangrove forests. This species is often associated with beds of eelgrass (Zostera marina) and river mouths. ("Cynoscion parvipinnis", 2012; Chao, et al., 2012; Fischer, et al., 1995; Froese and Béarez, 2012; Pondella and Williams, 2008; Pondella and Williams, 2009; Tenera Environmental, 2004)
Body coloration is gray to blue on the dorsal surface fading to silver to white sides with a pale ventral surface, while the area at the base of pectoral fin is darker than the body. The color of the interior of the mouth ranges from pale yellow to orange. The dorsal fin consists of 8 to 11 spiny rays and 21 to 24 soft rays. The anal fin has 2 spiny rays and 10 to 11 soft rays; the caudal fin is concave; lower jaw protruding, extending beyond upper jaw; upper jaw originating behind posterior margin of eye; 1 to 2 prominent canines on upper jaw; multiple tooth rows; chin without barbel or distinct pores; (9) 10 to 12 gill rakers with (8) 7 to 9 on lower limb of first arch; pelvic fins extending well beyond tips of short pectoral fins; interior of operculum dark; arch in lateral line above pectoral fin. Atractoscion nobilis by the absence of raised ridge along ventral surface in the former. (Agbayani, et al., 2011; Anònim, 1994; Cannon, 1953; Fischer, et al., 1995; Froese and Béarez, 2012; International Gamefish Association, 2001; Tenera Environmental, 2004)is distinguished from juvenile specimens of
This species is a pelagic broadcast spawner. (Fischer, et al., 1995)
Other members of the genus Cynoscion have been observed to produce audible vibrations by contracting muscles around the swim bladder (“croaking”) during mating season, presumably to alert potential mates to their presence. This behavior has yet to be formally documented in . Breeding interval is unknown; most likely once per breeding season. Spawning has been documented in Mexican populations in late April. (Agbayani, et al., 2011; Fischer, et al., 1995; Froese and Béarez, 2012; Tenera Environmental, 2004)
As this species is a broadcast spawner, there is no parental care for offspring. (Fischer, et al., 1995)
Most active at night, with peak activity occurring at sunrise and sunset in shallow water areas. During the day, the shortfin corvina tends to remain around cover such as deeper water; shaded areas around docks, piers and bridges; or channels in rocky areas. Individuals become increasingly solitary with age, forming temporary age-segregated schools of less than a dozen members. (Anònim, 1994; Cannon, 1953; Fischer, et al., 1995; Pondella and Williams, 2008; Pondella and Williams, 2009; Tenera Environmental, 2004)
As with other members of the family Sciaenidae, is anatomically capable of producing a “croaking” sound via the rapid and repeated contraction of muscles against the swim bladder. The shortfin corvina makes use of its lateral line, and well-developed eyes which are sensitive to, and highly perceptive of changes in ambient light levels to immediately locate its prey. Its olfactory sense detects potential prey located outside the range of its previous two senses. (Anònim, 1994; Fischer, et al., 1995; Froese and Béarez, 2012)
Shortfin corvina larvae feed upon copepods, amphipods, and other planktonic organisms, becoming increasingly piscivorous with age. Adults are opportunistic carnivores, feeding primarily on crustaceans and other fish at trophic level 2.8 and above. Important forage fishes include anchovies and silversides Anchoa and Atherinops, the “CIQ Complex Gobies” (Clevelandia ios, Ilypnus gilbert, and Quietula y-cauda) of the family Gobiidae (a primary food source for juvenile shortfin corvina); the California killifish (Fundulus parvipinnis), and viviparous perches of the family Embiotocidae. The California grunion (Leuresthes tenuis) is particularly important, and has been observed aggressively feeding upon them in shallow water during the grunion’s bimonthly summer spawning events. Shortfin corvina have been observed to repeatedly jump out of the water in pursuit of prey at dawn and dusk. Groups of up to 4 individuals have been seen driving schools of forage fish to the surface before breaking the surface of the water in what may represent a form of cooperative hunting effort. The enlarged canine teeth aid in the capture and subdual of larger forage fish. (Fischer, et al., 1995; Froese and Béarez, 2012; Pondella and Williams, 2008; Pondella and Williams, 2009; Tenera Environmental, 2004)
Pinnipeds in the families Phocidae and Otariidae are the most common predators of adult fish in protected bays. Due to their relatively large size, the only other predators of adult shortfin corvina are large sharks and groupers, with the giant sea bass (Stereolepis gigas), soupfin shark (Galeorhinus galeus) and broadnose sevengill shark (Notorynchus cepedianus) most prominent in the northern part of their range. In the southern range of , hammerhead sharks (Sphyrna spp.), the tiger shark (Galeocerdo cuvier), and various other Carcharhiniform sharks become prominent, in addition to several groupers in the genus Mycteroperca. (Anònim, 1994; Fischer, et al., 1995; Froese and Béarez, 2012; Tenera Environmental, 2004)
The shortfin corvina utilizes countershading as a means of camouflage against potential predators. Juveniles may aggregate in beds of the eelgrass Zostera marina for protection. (Tenera Environmental, 2004)
The primary impact of Atherinopsidae, Engraulidae, and Embiotocidae, as well as the California killifish (Fundulus parvipinnis), and the California halfbeak (Hyporhamphus rosae). This provides an interesting example of the way that two organisms need not be aware of the others’ existence to compete in the same ecosystem. (Fischer, et al., 1995; Froese and Béarez, 2012; Pondella and Williams, 2008; Pondella and Williams, 2009; Tenera Environmental, 2004)upon their ecosystem is via their predation on other fish species. In brackish water environments, the shortfin corvina directly competes with avian species for forage fishes in the families
There are no known negative effects of (Froese and Béarez, 2012)on humans.
Aaron Lerer (author), San Diego Mesa College, Paul Detwiler (editor), San Diego Mesa College, Jeremy Wright (editor), University of Michigan-Ann Arbor.
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.
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.
uses sound to communicate
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.
areas with salty water, usually in coastal marshes and estuaries.
an animal that mainly eats meat
uses smells or other chemicals to communicate
the nearshore aquatic habitats near a coast, or shoreline.
active at dawn and dusk
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.
animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature
an area where a freshwater river meets the ocean and tidal influences result in fluctuations in salinity.
fertilization takes place outside the female's body
union of egg and spermatozoan
A substance that provides both nutrients and energy to a living thing.
Animals with indeterminate growth continue to grow throughout their lives.
the area of shoreline influenced mainly by the tides, between the highest and lowest reaches of the tide. An aquatic habitat.
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).
makes seasonal movements between breeding and wintering grounds
eats mollusks, members of Phylum Mollusca
having the capacity to move from one place to another.
specialized for swimming
the area in which the animal is naturally found, the region in which it is endemic.
reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.
An aquatic biome consisting of the open ocean, far from land, does not include sea bottom (benthic zone).
chemicals released into air or water that are detected by and responded to by other animals of the same species
an animal that mainly eats fish
an animal that mainly eats plankton
the kind of polygamy in which a female pairs with several males, each of which also pairs with several different females.
mainly lives in oceans, seas, or other bodies of salt water.
breeding is confined to a particular season
reproduction that includes combining the genetic contribution of two individuals, a male and a female
uses touch to communicate
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).
the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.
movements of a hard surface that are produced by animals as signals to others
uses sight to communicate
animal constituent of plankton; mainly small crustaceans and fish larvae. (Compare to phytoplankton.)
2012. "Cynoscion parvipinnis" (On-line). Encyclopedia of Life. Accessed February 04, 2013 at http://eol.org/pages/1012533/overview.
California Department of Fish and Game. Final California Commercial Landings for 2010. Sacramento, California: California Department of Fish and Game. 2011. Accessed November 24, 2012 at http://www.dfg.ca.gov/marine/landings10.asp.
Agbayani, E., C. Elloran, K. Banasihan. 2011. "Length-Weight Relationship for Cynoscion parvipinnis" (On-line). FishBase. Accessed October 10, 2012 at http://www.fishbase.us/PopDyn/FishLWSummary.php?ID=3581&id2=5657&Genus=Cynoscion&Species=parvipinnis&variable_Length=28&variable_Length_required=Edit+box+can+not+be+blank..
Anònim, 1994. Atlas Pesquero de México. Mexico: Instituto Nacional de la Pesca.
Cannon, R. 1953. How to Fish the Pacific Coast. Menlo Park, California: Lane Publishing Company.
Chao, L., H. Espinosa, L. Findley, A. van der Heiden. 2012. "Cynoscion parvipinnis" (On-line). IUCN Red List of Threatened Species. Accessed November 01, 2012 at www.iucnredlist.org.
Fischer, W., F. Krupp, W. Schneider, C. Sommer, K. Carpenter, V. Niem, L. Chao. 1995. Guía FAO para la Identificación de Especies para los Fines de la Pesca Pacífico centro-oriental Volumen III. Vertebrados - Parte 2. Roma: Organización de las Naciones Unidas para la Agricultura y la Alimentación.
Froese, R., P. Béarez. 2012. "Cynoscion parvipinnis, Shortfin weakfish" (On-line). Accessed September 20, 2012 at http://www.fishbase.us/summary/Cynoscion-parvipinnis.html.
International Gamefish Association, 2001. "Database of IGFA Angling Records until 2001" (On-line). Accessed September 20, 2012 at http://www.igfa.org/.
Pondella, D., J. Williams. 2008. "Fisheries Inventory and Utilization of San Diego Bay, San Diego, California for Surveys Conducted in April and July 2008" (On-line pdf). Unified Port of San Diego. Accessed October 10, 2012 at http://www.portofsandiego.org/public-documents/doc_download/1902-2008-bay-wide-fish-survey.html.
Pondella, D., J. Williams. 2009. "Fisheries Inventory and Utilization of San Diego Bay, San Diego, California for Surveys Conducted in June 2009" (On-line pdf). Unified Port of San Diego. Accessed October 10, 2012 at http://www.portofsandiego.org/public-documents/doc_download/2069-vrg-fish-report-2009.html.
Tenera Environmental, 2004. "SBPP Cooling Water System Effects on San Diego Bay, Volume II: Compliance with Section 316(b) of the Clean Water Act for the South Bay Power Plant" (On-line). Accessed September 22, 2012 at http://swrcb2.swrcb.ca.gov/sandiego/board_decisions/adopted_orders/2004/2004_0154techrptb.pdf.