dcsimg

Diagnostic Description

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Diagnosis: The larvae of all Sparisoma may well be identical, and DNA sequencing is required to identify species. Transitional recruits develop the basic markings probably shared by all members of the genus, but small juveniles of Sparisoma acquire distinct patterns that separate most, if not all, regional species. S. viride diverges from the remainder of the genus the earliest, with some individuals smaller than 10 mm SL showing a distinct pattern of markings, in particular an undivided prominent white bar on the caudal fin base.

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Comprehensive Description

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Description: This type shares the characteristic markings of larval and transitional Sparisoma. Recruits become distinct early on when the leukophores on the base of their caudal fin coalesce into a distinct white bar and they develop rows of round white spots, with the two above the pectoral fin most visible. Characteristically, there are no melanophores extending into the white bar (at least until about 15 mm SL, but by then the white bar and rows of white spots are clearly prominent).

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Diagnostic Description

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Relationship between fork length (FL) and maximum body depth (D): D = 0.10 + 0.33(FL); FL = -0.40 + 3.06(D), for n = 79, length range (cm, FL) = 13.5-25.5 (Ref. 3191). A distinctive, colorful and abundant fish. Young adults and females with scales outlined in darker gray; often bright red below. Super males green, with bright yellow spot at upper edge of gill cover, yellow bar at base of tail, curved orange-yellow mark on caudal fin rays (Ref. 26938). Initial phase fish with a brown head, the scales of the upper two-thirds of the body with pale centers and dark brown edges, the lower third of body and fins bright red. Terminal phase males are green with three diagonal orange bands on upper half of head
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Recorder
Rodolfo B. Reyes
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Life Cycle

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The type of reproductive behavior is related to the color phase of the males involved.
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Susan M. Luna
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Morphology

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Dorsal spines (total): 9; Dorsal soft rays (total): 10; Analspines: 3; Analsoft rays: 9
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Trophic Strategy

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Has been observed to graze on live corals like Montastrea annularis probably due to the absence of adequate seagrasses and large seaweeds in the area (Ref. 6496). Also cleaned by Thalassoma noronhanum observed at Fernando de Noronha Archipelago off northeastern Brazil (Ref. 36301) and by Elacatinus figaro observed off the coast of São Paulo, southeastern Brazil (Ref. 40102). Herbivore (Ref. 33499, 57616).
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Biology

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Inhabits coral reefs with clear water (Ref. 13628). Young may be found in seagrass beds and other heavily vegetated bottoms. Feeds mainly on soft algae, but has been observed to graze on live corals like, Montastraea annularis (Ref. 6496). Produces a significant amount of sediment through bioerosion using its strong beak-like jaws and constantly re-growing teeth (Ref. 6485). Protogynous; strictly diurnal, spends the night sleeping on the bottom (Ref. 5221). Found singly or small in small groups.
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Importance

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fisheries: minor commercial; aquarium: commercial; price category: high; price reliability: very questionable: based on ex-vessel price for species in this family
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Comprehensive Description

provided by Smithsonian Contributions to Zoology
Sparisoma viride (Bonnaterre)

Scarus viridis Bonnaterre, 1788, p. 96, pl. 50: fig. 193.

Sparisoma viride.—Schultz, 1958, p. 114, fig. 28.—Winn and Bardach, 1960, pp. 31–33, fig. 2B [males].—Randall and Randall, 1963, p. 54.—Cervigon, 1966, p. 623, figs. 267–268.—Stark and Davis, 1966, p. 339 [night habits].

Sparus abildgaardi Bloch, 1791, p. 22, pl. 259.

Sparisoma abildgaardi.—Schultz, 1958, p. 121, pls. 4C, 24A, B.—Winn and Bardach, 1960, p. 33–35 [females].—Randall and Randall, 1963, pp. 54.

See Schultz (1958, pp. 114, 121) for other synonyms.

No ridge on upper dental plate and canines, if present, behind middle of length of dental plate; dermal flap of anterior nostril, with multifid cirri in adults, more ribbon-like in young; interorbital space flattish or nearly so; membranes just behind tips of dorsal spines usually without cirrus, or rarely 1 or 2, in addition to tip of dorsal spine, which bears a terminal cirrus.

Coloration of males: opercular flap with round white (yellow) spot, posterior edge of opercle white (red); caudal fin deeply forked, with a lunate white (red) bar submarginally and distal edge green; on base of caudal fin and peduncle 1 to 3 light (orange or yellow) spots; light streak (red) bounded by green from corner of mouth across cheek; no dark spot on base of pectoral.

Coloration of females (abilgaardi): margins of scales dark brown, centers pale, several isolated ones white, arranged in 6 vertical rows; posterior margin of gill cover black (reddish brown); lower part of body below level of pectoral base white (blood red), caudal fin red, and in young a broad white bar occurs on basal one-third, distal two-thirds barred.

Winn and Bardach (1960, pp. 31–33) determined that abilgaardi represents the immature and females of viride.

RANGE. Central and western Atlantic Ocean.

Sparisoma aurofrenatum (Cuvier and Valenciennes)

Scarus aurofrenatus Cuvier and Valenciennes, 1839, p. 191.

Sparisoma aurofrenatum.—Schultz, 1958, p. 115, figs. 29, 30.—Winn and Bardach, 1960, p. 33.—Randall and Randall, 1963, p. 54.—Cervigon, 1966, p. 619, figs. 264–265.

See Schultz (1958, p. 115) for other synonyms.

Characterized by having a flattish interorbital space (slightly convex in young); anterior nasal tentacle ribbon-like without cirri in specimens shorter than 40 mm, but cirri developing on larger ones; membranes behind tips of dorsal spines without cirri; canines occurring on adults, absent on immature.

Coloration of adult males: White streak from corner of mouth past lower edge of orbit ending on naked area behind eye; white spot or dash may occur just behind eye; a few small brown spots occurring on 3rd or 4th scales in row below lateral line, then below or behind them a white spot; tips of outer caudal fin rays brownish; edges of dorsal and anal fins dusky; dorsal base of pectoral dusky.

Females and immature specimens have a white saddle-like spot on the dorsal edge of the caudal peduncle just behind the dorsal fin base; a silvery spot may occur on the middle of the opercle; the young have a row of white scales along the base of the dorsal fin; some immature females are plain dark brown without a white peduncular spot, but with brown crossbars on the under side of the head as in other species of Sparisoma.

Both sexes plain dark brown on shoulder area under opercular apparatus; white gland dorsally sharply contrasting with blackish around it.

RANGE.—Central and western Atlantic Ocean.

Calotomus Gilbert, 1890, p. 70.

Characterized by having 4 median predorsal scales; flexible dorsal spines, gill membranes joined to isthmus without free fold; anterior nasal opening with broad dermal cirrus; internal edge of coalesced teeth serrated; and externally on dental plate 2 to 4 rows (more on adults) of obliquely arranged imbricated pointed incisor-like teeth; midside of upper dental place may have 1 to 4 canines, hooked out and backward; gill rakers 2 to 4+1+7 to 13.

RANGE.—Eastern, central and western Pacific Ocean, Hawaiian Islands, Indian Ocean, and Red Sea.

Calotomus spinidens (Quoy and Gaimard)

Scarus spinidens Quoy and Gaimard, 1824, p. 289.—Bauchot and Guibè, 1960, p. 299 [holotype no. 571 in Paris Museum].

Calotomus spinidens—Schultz, 1958, p. 124, pls. 5B, 24C; 1960, p. 250, pl. 108C, 109C—Briggs, 1964, p. 707.—Munro, 1967, p. 430, fig. 821 [New Guinea].

Cryptotomus spinidens.—Kamohara, 1963, p. 21, pl. 6: fig. 4 [Okinawa].—Marshall, 1965, p. 320.

Callyodon carolinus Cuvier and Valenciennes, 1839, p. 291.—Bauchot and Guibè, 1960, p. 290 [holotype no. 560].

Callyodon sandwicensis Cuvier and Valenciennes, 1839, p. 295.—Bauchot and Guibè, 1960, p. 290 [holotype no. 568].

Calotomus sandwicensis.—Gosline and Brock, 1960, p. 236 [Hawaiian Islands].

Callyodon genistriatus Cuvier and Valenciennes, 1839, p. 293.—Bauchot and Guibè, 1960, p. 291 [holotype no. 576].

Characterized by having the caudal fin truncate in young, then concave, finally in adults deeply concave; length of middle rays of caudal fin three-fourths to equal to longest pectoral fin ray.

Coloration a mottled gray and reddish brown background, bright red mottlings in fins, and lower jaw with red blotches; radiating from eye 2 prominent bands (red when alive) extending to rear of mouth; snout barred; dark blotch between dorsal spines I and II and half-grown specimens; base of last 3 soft dorsal rays may have black spot; caudal fin with white distal margin sometimes bordered submarginally with dark line; anus black under scaly sheath; base of pectoral brown in small specimens.

The following collections were made during the IIOE, Cruise 9 of the Anton Bruun: USNM 201565 Sta. FT–2, Market, Mombasa, Kenya, 16 November 1964, 1 spec. 235 mm; USNM 201567, Sta. HA–17, channel reef at SE end West Island [Ile Picard], Aldabra Islands, 4 December 1964, 1 spec, 205 mm; USNM 201566, Sta. RS–37, Farquhar Islands, 6 December 1964, 1 spec, 145 mm; USNM 201568, Sta. RS–41, KA39, Amirantes Island, 10 spec.

The following are from Diego Garcia Atoll: Sta. HA67–3, 12 June 1967, 1 spec, 125 mm; Sta. HA67–16, 22 June 1967, 2 spec., 56 and 99 mm.

RANGE. Revillagigedos Islands, Hawaiian Islands, central and western Pacific Ocean, Indian Ocean, and Red Sea.

Calotomus japonicus (Cuvier and Valenciennes)

Callyodon japonicus Cuvier and Valenciennes, 1839, p. 294, pl. 406.—Bauchot and Guibè, 1961, p. 259, [lectotype no. 8229 in Paris Museum].

Calotomus japonicus.—Schultz, 1958, p. 125, pls. 5A, 24D.—Munro, 1967, p. 431, fig. 822 [New Guinea].

Characterized by a rounded caudal fin at all sizes, with the distal edge dusky, not white; length of middle caudal fin rays equal in young to or longer than longest pectoral fin ray.

General background coloration reddish brown, with numerous tiny light spots on scales; also several larger white spots on upper sides; and 2 rows of white spots on lower side; fins mottled; head with numerous white specks; caudal fin barred.

The following specimens were collected during the IIOE by the Anton Bruun: From Nossi-Bè, Madagascar: USNM 201510, Field No. JR–53, 30 January 1964, 8 spec, 50–137 mm; USNM 201503, Field No. JR–75, 17 February 1964, 12 spec, 56–126mm;USNM 201509, Tulear Harbor, Madagascar, 11 August 1964, 5 spec, 46–66 mm. From Andromache Reef, south of entrance to Port Kilindini, Mombasa Harbor: USNM 201513, Sta. HA–1, 15 November 1964; 1 spec, 60 mm; USNM 201507, Sta. HA–2, 16 November 1964, 7 spec, 33 to 85 mm. From the Comoro Islands: USNM 201508, Sta. HA–8, 24 November 1964, 11 spec, 40–67 mm; USNM 201504, Sta. HA–9, 24 November 1964, 0–9 ft., 2 spec, 35–40 mm. From the Farquhar Islands USNM 201506, Sta. RS–37, 6 December 1964, 17 spec, 50–131 mm; USNM 201512, Sta. HA–18, 6 December 1964, 1 spec, 59 mm; USNM 201503, Cruise 9, Sta. RS–41; KA–39, Amirantes Island, 10 spec, 75–154 mm.

In addition, the following were collected at Diego Garcia Atoll, Chagas Archipelogo: Sta. HA67–2, 11 June 1967, 2 spec, 26 and 47 mm; Sta. HA67–16, 22 June 1967, 6 spec., 45–93 mm; Sta. HA67–49, 20 July 1967, 3 spec, 68–113 mm.

The following collection is from the Te Vega Expedition, Cruise 6: USNM 201511, Sta. 243, lagoon east side of Puk Puk Island, Bougainville, Solomon Islands, 9 March 1965, 1 spec, 93 mm.

RANGE.—Hawaiian Islands, western Pacific Ocean, and Indian Ocean.

Leptoscarus Swainson, 1839, pp. 172, 226.

Characterized by having 4 median predorsal scales; flexible dorsal spines, gill membranes broadly joined to isthmus without free fold; no free, imbricate, incisorlike teeth present externally on dental plates; coalesced teeth of dental plate with external canines on upper jaw of adult males absent in young and on females.

Leptoscarus vaigiensis (Quoy and Gaimard)

Scarus vaigiensis Quoy and Gaimard, 1824, p. 288.—Bauchot and Guibè, 1960, p. 298 [holotype no. 567 in Paris museum].

Leptoscarus vaigiensis.—Schultz, 1958, p. 126, pls. 4A, 25A, B; 1960, p. 251, pls. 108F, 109D, E.—Kamohara, 1963, p. 121, pl. 6: fig. 3 [Japan].—Marshall, 1965, p. 319, pl. 46.—Munro, 1967, p. 430, fig. 820 [New Guinea].

Scarus bottae Cuvier and Valenciennes, 1839, p. 262.—Bauchot and Guibè, 1960, p. 292 [syntypes 2456, 2457, 2458].

Leptoscarus caeruleopunctatus.—Marshall, 1965, p. 319.

Scarichthys coeruleopunctatus.—Ben-Tuvia, 1966, p. 271 [Mediterranean Sea].

See Schultz (1958, p. 126) for other synonyms.

Background coloration reddish brown, lighter brown ventrally; head, body, and fins may be richly speckled with dark brown dots (blue when alive), pectoral base blackish; ventrally 3 lengthwise rows of scales having brown centers, giving appearance of 3 light and dark alternating streaks behind and below pectoral fin base; males with canine teeth on upper dental plates, absent on females.

The following specimens were collected during the IIOE by the Anton Bruun: From Nossi-Bè, Madagascar: USNM 201535, Sta. JR–53, 20 January 1964, 7 spec, 64–220 mm; USNM 201528, Sta. JR–76, 18 February 1964, 1 spec, 30 mm; USNM 201532, Tulear Harbor, Madagascar, 11 August 1964, 27 spec, 39–98 mm; USNM 201526, Sta. 420, Field No. LK–64–100, dip net in Sargassum weed, 3°7′S, 40°39′E, 5 November 1964, 1 spec, 36 mm. From Mombosa Harbor: USNM 201539, Sta. HA–2, 2 spec, not measured; USNM 201537, Sta. HA–2, 16 November 1964, 22 spec, 22–190 mm; USNM 201538, Sta. FT–2, 16 November 1964, 1 spec, 225 mm. From the Comoro Islands: USNM 201530, Sta. HA–8, 24 November 1964, 1 spec, 47 mm; USNM 201527, Sta. HA–9, 24 November 1964, 1 spec, 34 mm; USNM 201533, Sta. FT–11, market and Msasani Bay, Dar-es-Salaam, 30 November 1964, 4 spec, 47–104 mm. From the Farquhar Islands: USNM 201531, Sta. HA–18, 6 December 1964, 26 spec, 17–125 mm; USNM 201534, Sta. RS–37, 6 December 1964, 2 spec, 76–95 mm; USNM 201536, Sta. HA–19, Amirante Islands, St. Joseph Island, Resource Island, 10 spec, 22–185 mm. From Diego Garcia Atoll: Sta. HA–67–16, 22 June 1967, 1 spec, 78 mm.

RANGE.—Central and western Pacific Ocean, Indian Ocean, Red Sea, and Mediterranean Sea through Suez Canal.

Crypototomus Cope, 1871, p. 462.

Characterized by having 4 median predorsal scales; dorsal spines flexible; gill membranes broadly joined to isthmus with a narrow free fold across isthmus; elongate form, pointed snout, angle between dorsal and ventral profile of head 40° to 50°; no dermal cirrus on anterior nostril with raised rim; external incisorlike teeth at front of mouth, teeth slanting forward; canine teeth present on side of upper jaw of half-grown specimens and adults.

RANGE.—Western Atlantic Ocean.
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bibliographic citation
Schultz, Leonard P. 1969. "The taxonomic status of the controversial genera and species of parrotfishes with a descriptive list (family Scardiae)." Smithsonian Contributions to Zoology. 1-49. https://doi.org/10.5479/si.00810282.17

Stoplight parrotfish

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The stoplight parrotfish (Sparisoma viride) is a species of marine ray-finned fish, a parrotfish from the family Scaridae, inhabiting coral reefs in Florida, Caribbean Sea, Gulf of Mexico, Bermuda and as far south as Brazil.[3] It mainly feeds on algae by scraping and excavating it with its teeth. Like most of its relatives, it is able to change sex.

The common name, stoplight, comes from the marked yellow spot near the pectoral fin, which is clearly visible only in specimens in the terminal phase.

Sex Change & Coloring

The stoplight parrotfish is a protogynous hermaphrodite that shows full sexual dichromatism, meaning that it changes its sex from female to male during its lifespan, and its color changes with its sex change.[4] The sex change is most likely due to the control of hormones, in particular, 11-ketetestosterone (11-KT).[5] The timing of the sex change can vary depending on population density, growth, and mortality rates. Early sex changes may occur if sexually active individuals have a higher mortality rate or have reduced growth rates.[6]

Stoplight parrotfish in its initial phase

The stoplight parrotfish has 3 life phases: juvenile, initial, and terminal. The colors of the stoplight parrotfish in the initial phase, when it could be either a male or a female, are dramatically different from those in the terminal phase, when it is definitely a male.[5] During the juvenile and initial phase, the parrotfishes are colored brown with a red belly. During the terminal phase, the parrotfishes are a vivid green color with yellow spots on the tail base of their caudal fin.[4][7] However, some males do not change color at the same time they change sex, therefore becoming female-mimic males (also termed initial phase males). During the initial phase, about 4% of the smaller parrotfish individuals are males.[7]

Habitat

The stoplight parrotfish inhabit shallow coral reefs not disturbed by humans in Florida, the Caribbean Sea, Gulf of Mexico, Bermuda and Brazil.[4] They are only active during the day and spend most of their time foraging, swimming, or hovering.[4][7] At night, they remain hidden under coral boulders.[4] Large individuals typically spend more time swimming and spend a significant amount of time sheltering among crevices,[7] while smaller individuals spend more time hovering.[7] The stoplight parrotfish have a high density in areas of higher algal production. As adults, the stoplight parrotfish are site-attached with limited home ranges.[6]

In the Florida Keys, the stoplight parrotfish were found most frequently in areas with high cover of the macroalgae Dictyota. They have also been found to select for the branching coral Porites porites, however Dictyota are an effective recruitment substrate when branching corals are not available.[8]

Due to its abundance in the Caribbean, the stoplight parrotfish are very ecologically important there.[6]

Onshore and Offshore Reefs

Onshore coral reefs have a greater proportion of older juvenile fish, suggesting that the mortality and/or emigration of adults is more common onshore.[8] Stoplight parrotfishes on offshore coral reefs have a greater average standard length, greater mean asymptotic size, and live twice as long as other fish from onshore coral reefs. Fish onshore were no older than 4 years, while the fish offshore reached 7–8 years. The age difference between offshore and onshore reefs could be due to the stoplight parrotfish migrating from onshore to offshore reefs with age, however, there is no evidence of ontogenetic migration.[6]

Feeding & Foraging

The stoplight parrotfish employs a scraping and excavating grazing mode and feeds almost exclusively on algae that are associated with dead coral substrates.[4] They have higher grazing rates and assimilation efficiencies in areas with high-quality food.[6]

Their preferred food types are large, sparse turfs growing on carbonate substrates that are inhibited by endolithic algae. Algae have high levels of proteins, a high energetic value, along with a high yield, making it preferable to the stoplight parrotfish. As facultative corallivores, adult fish will occasionally feed on living corals (mainly Montastrea annularis). In healthy coral reef environments, the detriment of coral-feeding by parrotfish tends to be offset by the benefits of their algal feeding. In declining coral reefs, however, corallivory by parrotfish may act synergystically with other stressors to depress coral growth and recovery.[9] Crutose corallines are not preferred, whether or not they do or do not have algal turf.[4]

Their foraging strategy is called “search and nip” and they spend short bouts of energy on swimming, feeding, and hovering.[7]

Growth Rate

The stoplight parrotfish grow continuously throughout life[4] and their growth rate increases with higher food availability.[6] The largest class of stoplight parrotfish is when they are in their terminal phase.[6]

Its typical length is between 1 and 1.5 ft (30–45 cm),[3] but it can reach up to 2 ft (64 cm).[2] It is normally found during the day at depths between 15 and 80 ft (5–25 m),[3] but can be found from 10 to 165 ft (3–50 m)[2]

Reproduction

Stoplight parrotfishes engage in reproductive activity throughout the year.[4] They are harem-forming fishes and territorial terminal phase males defend areas that are shared with 1-14 initial phase parrotfishes, with whom they mate. There is more territorial defense in areas with high-quality food.[6] Single terminal phase males also defend the deeper reef from conspecifics.[4]

Stoplight parrotfish males will often control territories containing many sexually mature females to breed with. Males that have territories and those that don't will have vastly different levels of testosterone.[10]

References

  1. ^ Rocha, L.A.; Choat, J.H.; Clements, K.D.; Russell, B.; Myers, R.; Lazuardi, M.E.; Muljadi, A.; Pardede, S.; Rahardjo, P. (2012). "Sparisoma viride". IUCN Red List of Threatened Species. 2012: e.T190734A17779745. doi:10.2305/IUCN.UK.2012.RLTS.T190734A17779745.en. Retrieved 19 November 2021.
  2. ^ a b c Froese, Rainer; Pauly, Daniel (eds.) (2019). "Sparisoma viride" in FishBase. December 2019 version.
  3. ^ a b c Humann, DeLoach (2002). Reef Fish Identification - Florida Caribbean Bahamas. New World Publications, Inc. ISBN 1-878348-30-2.
  4. ^ a b c d e f g h i j Bruggemann, J. Henrich; van Oppen, Madeleine J.H.; Breeman, Anneke M. (March 17, 1994). "Foraging by the stoplight parrotfish Sparisoma viride. I. Food selection in different, socially determined habitats" (PDF). Marine Ecology Progress Series. 106: 41–55. doi:10.3354/meps106041.
  5. ^ a b Cardwell, J.R.; Liley, N.R. (1991). "Hormonal control of sex and color change in the stoplight parrotfish, Sparisoma viride". General and Comparative Endocrinology. 81 (1): 7–20. doi:10.1016/0016-6480(91)90120-U. PMID 2026318.
  6. ^ a b c d e f g h Paddack, M. J.; Sponaugle, S.; Cowen, R. K. (December 2009). "Small-scale demographic variation in the stoplight parrotfish Sparisoma viride". Journal of Fish Biology. 75 (10): 2509–2526. doi:10.1111/j.1095-8649.2009.02451.x. PMID 20738505.
  7. ^ a b c d e f Hanley, Fred (1984-12-14). "Time-budgeting and foraging strategy of the stoplight parrotfish Sparisoma viride Bonnaterre, in Jamaica". Journal of Experimental Marine Biology and Ecology. 83 (2): 159–177. doi:10.1016/0022-0981(84)90043-1. ISSN 0022-0981.
  8. ^ a b Paddack, Mj; Sponaugle, S (2008-10-13). "Recruitment and habitat selection of newly settled Sparisoma viride to reefs with low coral cover". Marine Ecology Progress Series. 369: 205–212. doi:10.3354/meps07632. ISSN 0171-8630.
  9. ^ Rotjan, Randi D.; Lewis, Sara M. (2008-09-11). "Impact of coral predators on tropical reefs". Marine Ecology Progress Series. 367: 73–91. doi:10.3354/meps07531. ISSN 0171-8630.
  10. ^ Cardwell, J. “Androgen Control of Social Status in Males of a Wild Population of Stoplight Parrotfish, Sparisoma Viride (Scaridae)*1.” Hormones and Behavior, vol. 25, no. 1, Mar. 1991, pp. 1–18., doi:10.1016/0018-506x(91)90035-g.

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Stoplight parrotfish: Brief Summary

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The stoplight parrotfish (Sparisoma viride) is a species of marine ray-finned fish, a parrotfish from the family Scaridae, inhabiting coral reefs in Florida, Caribbean Sea, Gulf of Mexico, Bermuda and as far south as Brazil. It mainly feeds on algae by scraping and excavating it with its teeth. Like most of its relatives, it is able to change sex.

The common name, stoplight, comes from the marked yellow spot near the pectoral fin, which is clearly visible only in specimens in the terminal phase.

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