Overview
Comprehensive Description
Biology
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Randall, J.E., G.R. Allen and R.C. Steene 1990 Fishes of the Great Barrier Reef and Coral Sea. University of Hawaii Press, Honolulu, Hawaii. 506 p. (Ref. 2334)
http://www.fishbase.org/references/FBRefSummary.php?id=2334&speccode=13770
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Distribution
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Myers, R.F. 1991 Micronesian reef fishes. Second Ed. Coral Graphics, Barrigada, Guam. 298 p. (Ref. 1602)
http://www.fishbase.org/references/FBRefSummary.php?id=1602&speccode=4306
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Range Description
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Geographic Range
Blue streak wrasses inhabit Indo-pacific coral reefs, including the Great Barrier Reef. They range from Queensland and the South Seas through the East Indies to the Red Sea, Zanzibar and Mauritius (Marshall, 1964)
Biogeographic Regions: pacific ocean (Native )
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MacNae, W. & M. Kalk (eds) (1958). A natural history of Inhaca Island, Mozambique. Witwatersrand Univ. Press, Johannesburg. I-iv, 163 pp.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=6266
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Anon. (1996). FishBase 96 [CD-ROM]. ICLARM: Los Baños, Philippines. 1 cd-rom pp.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=5909
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Randall, J.E. (1992). Red Sea Reef Fishes. Immel Publishing.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=6091
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Anon. (2000). FishBase 2000 [CD-ROM]. ICLARM: Los Baños, Laguna, Philippines. 4 cd-roms pp.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=6542
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Smith, J.L.B. & M.M. Smith (1963). The fishes of Seychelles. Department of Ichthyology, Rhodes University. Grahamstown.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=5926
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Bock, K.R. (1996). Checklist of the reef fishes of Diani and Galu, Kenya. Journal of East African natural History 85: 5-22.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=6357
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Bock, K.R. (1975). Preliminary checklist of the fishes of the south bank, Kilifi Creek, Kenya. Journal of the East Africa Natural History Society and National Museum 148.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=6136
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McClanahan, T.R. (1994). Kenya coral reef lagoon fish: effects of fishing, substrate complexity, and sea urchins. Coral Reefs 13: 231-241
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=5911
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Letourneur, Y., M. Harmelin-Vivien & R. Galzin (1993). Impact of hurricane Firinga on fish community structure on fringing reefs of Reunion Island, S.W. Indian Ocean. Environmental Biology of Fishes 37: 109-120
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=6048
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Physical Description
Morphology
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Randall, J.E., G.R. Allen and R.C. Steene 1990 Fishes of the Great Barrier Reef and Coral Sea. University of Hawaii Press, Honolulu, Hawaii. 506 p. (Ref. 2334)
http://www.fishbase.org/references/FBRefSummary.php?id=2334&speccode=13770
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Physical Description
Adult blue streak wrasses usually grow to be 4 inches long (Grant,1978).
Wrasses possess a smooth, compressed, elongate body with a pointed snout. They have small mouths with prominent lips. They have jaws and teeth, particularly 2 canines that are curved anteriorly in each jaw.
Wrasses have a rounded caudal fin along with a dorsal fin consisting of 9 spines and 9-11 rays and an anal fin with 2-3 spines and 9-10 rays (Marshall, 1964). Wrasses have very small scales and the head is normally scaleless.
Blue streak wrasses are brilliant blue with a broad jet-black band that runs from the tip of the snout to the end of the tail, starting out narrow at the anterior end and gradually broadening towards the posterior end. This band usually takes up most of the tail, except the upper and lower rays which are a shade of blue (Marshall, 1966). Young wrasses are sometimes all black, except for a pale streak along the lower, upper and back caudal rays (Marshall, 1964).
The colors of young and adult wrasses differ (Smith, 1965). They are also known to change colors based on mood (Grant, 1978).
There is no geographic variation in morphology or coloration.
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Size
Max. size
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Allsop, D.J. and S.A. West 2003 Constant relative age and size at sex change for sequentially hermaphroditic fish. J. Evol. Biol. 16(2003):921-929. (Ref. 55367)
http://www.fishbase.org/references/FBRefSummary.php?id=55367&speccode=3660
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Robertson, D.R. 1974 A study of the ethology and reproductive biology of the labrid fish, Labroides dimidiatus at Heron Island, Great Barrier Reef. University of Queensland, Brisbane. 295 p. Ph.D dissertation. (Ref. 3426)
http://www.fishbase.org/references/FBRefSummary.php?id=3426&speccode=5459
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Diagnostic Description
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Randall, J.E., G.R. Allen and R.C. Steene 1990 Fishes of the Great Barrier Reef and Coral Sea. University of Hawaii Press, Honolulu, Hawaii. 506 p. (Ref. 2334)
http://www.fishbase.org/references/FBRefSummary.php?id=2334&speccode=13770
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Description
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Anon. (1996). FishBase 96 [CD-ROM]. ICLARM: Los Baños, Philippines. 1 cd-rom pp.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=5909
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Ecology
Habitat
Environment
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Lieske, E. and R. Myers 1994 Collins Pocket Guide. Coral reef fishes. Indo-Pacific & Caribbean including the Red Sea. Haper Collins Publishers, 400 p. (Ref. 9710)
http://www.fishbase.org/references/FBRefSummary.php?id=9710&speccode=13770
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Baensch, H.A. and H. Debelius 1997 Meerwasser atlas. Mergus Verlag GmbH, Postfach 86, 49302, Melle, Germany. 1216 p. 3rd edition. (Ref. 27115)
http://www.fishbase.org/references/FBRefSummary.php?id=27115&speccode=4306
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Habitat and Ecology
It feeds on crustaceans ectoparasites and mucus of fishes which gather at specific cleaning ‘stations’ for attention (Pott 1973). Males and females are the same in colour, juveniles are black with a single blue stripe running from snout to the upper part of caudal fin.
It is active in daytime and is reported to be able to produce a protective mucous cocoon at night. Seasonal fluctuation of the activity rate has been observed with almost all individuals always active during late spring and early summer (Kuwamura 1981).
In Japan, spawning occurred within 4-5 months of the year, from late May to early September. Larvae of about 1.8 mm in total length hatch at 30 hours after spawning (Kuwamura 1981).
This species is monochromatic, spawns in harem. Spawning ascent distance was about three m with rapid ascending speed. Spawning activities were seen in March, May, June and November at Enewetak Atoll, Marshall Islands (Colin and Bell 1991). The size of eggs is approximately 0.64 mm and spherical in shape. Eggs contained multiple oil globules
Maximum size of species has been recorded at 22 cm (TL) in New Caledonia and maturity is reached at a size of about six cm TL (Kuwamura 1981, M. Kulbicki pers. comm.). All of the larger adults have an almost completely developed ventroanterior hook in the caudal fin. Maximum lifespan is estimated to be four years (Allsop and West 2003) and minimum population doubling time is approximately 1.4-4.4 years (Froese and Pauly 2008).
It shows cleaning behaviour, which only occurs during the day and particularly in the early morning (Grutter 1996). In captivity it is affected by abundance and size-frequency distribution of the monogenean parasites on the host of fishes, which was more pronounced on larger fish than on small fish (Grutter et al. 2002). It spends 60 to 154 more times cleaning larger fishes (> 12.5 cm SL) than medium (9.5 to 12.5 cm SL) or small sized fish (
It consumes a large number of parasites (1218 +/- 118) each day or 4.8 +/- 0.4 parasites per minute (Grutter 1996) and most of the prey items were juvenile gnathiid isopods (Grutter 1997). The biomass of gnathiids in the diet in New Caledonia was lower than at Lizard Island, but higher than at Heron Island, suggesting that the role of gnathiids in cleaning behaviour is variable (Grutter 1999).
At One Tree Lagoon on the Great Barrier Reef, overall mortality during first year for L. dimidiatus was 50%, juveniles do not shelter within the substratum and displayed relatively high mortality over the first twelve months (Eckert 1987). The average annual mortality ofL. dimidiatus was 11.1 +/- 2.2 %.
Systems
- Marine
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Striped cleaner wrasses tend to dwell in coral or rocky areas on coral reefs (Roughley, 1951). They are commonly found in waters adjacent to shallow coral outcrops along the Great Barrier Reef (Grant, 1978). They are also seen in tide-pools. (Smith, 1965)
They are not migratory.
Aquatic Biomes: reef
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Water temperature and chemistry ranges based on 311 samples.
Environmental ranges
Depth range (m): 0.15 - 99
Temperature range (°C): 20.792 - 29.336
Nitrate (umol/L): 0.019 - 5.255
Salinity (PPS): 32.185 - 40.307
Oxygen (ml/l): 3.591 - 5.079
Phosphate (umol/l): 0.055 - 0.567
Silicate (umol/l): 0.567 - 10.063
Graphical representation
Depth range (m): 0.15 - 99
Temperature range (°C): 20.792 - 29.336
Nitrate (umol/L): 0.019 - 5.255
Salinity (PPS): 32.185 - 40.307
Oxygen (ml/l): 3.591 - 5.079
Phosphate (umol/l): 0.055 - 0.567
Silicate (umol/l): 0.567 - 10.063
Note: this information has not been validated. Check this *note*. Your feedback is most welcome.
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From 1 to 40 meters.
Habitat: reef-associated.
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Trophic Strategy
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Sano, M., M. Shimizu and Y. Nose 1984 Food habits of teleostean reef fishes in Okinawa Island, southern Japan. University of Tokyo Bulletin, no. 25. v,128p. University of Tokyo Press, Tokyo, Japan. 128 p. (Ref. 6110)
http://www.fishbase.org/references/FBRefSummary.php?id=6110&speccode=9950
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Food Habits
Wrasses are carnivorous. Their diet consists primarily of parasitic copepods and other invertebrates that are taken from the mouth and gill openings of larger fish. They also feed occasionally on free-swimming crustaceans.
Blue streak wrasses are known as common cleaner fish that set up cleaning stations on various parts of coral reefs, usually 3-10ft. deep. They attract larger fish to their stations by making strange, oscillatory swimming movements, and the fish then stop to get cleaned. Wrasses enter the mouth and gill openings and remove any ectoparasites and diseased tissue. The larger fish not only refrain from devouring these small cleaner fish, but actually readily open their mouth and gill cavities so that they are able to clean.
This is clearly a mutualistic relationship between cleaner wrasses and various larger fish of the ocean (Grant, 1978).
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Life History and Behavior
Life Cycle
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Ross, R.M. 1990 The evolution of sex-change mechanisms in fishes. Environ. Biol. Fish. 29(2):81-93. (Ref. 32168)
http://www.fishbase.org/references/FBRefSummary.php?id=32168&speccode=8272
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Life Expectancy
Lifespan/Longevity
Average lifespan
Status: captivity: 4 years.
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Reproduction
Wrasses practice external fertilization in which the female's eggs are released into the water. Mating usually occurs at twilight (Flying Fish Express)
Large males defend reef territories and attract multiple females to these territories, usually by performing a beautiful mating dance. Females live within these territories and spawn with the male. Fertilized eggs form planktonic larvae that move freely with the ocean currents. If the territorial male leaves or dies, the most dominant female will take his role and become male within the next 24 hours. She assumes the territory and mates with the rest of the females.
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Molecular Biology and Genetics
Molecular Biology
Barcode data: Labroides dimidiatus
There are 31 barcode sequences available from BOLD and GenBank. Below is a sequence of the barcode region Cytochrome oxidase subunit 1 (COI or COX1) from a member of the species. See the BOLD taxonomy browser for more complete information about this specimen and other sequences.
-- end --
Download FASTA File
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Statistics of barcoding coverage: Labroides dimidiatus
Public Records: 29
Specimens with Barcodes: 43
Species With Barcodes: 1
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Conservation
Conservation Status
IUCN Red List Assessment
Red List Category
Red List Criteria
Version
Year Assessed
Assessor/s
Reviewer/s
Contributor/s
Justification
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US Federal List: no special status
CITES: no special status
IUCN Red List of Threatened Species: least concern
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Trends
Population
It is common in the southern coral areas of the Ryukyu Islands and Ogasawara Islands (Kataoka et al. 1970), on the inshore rocky reefs, whereas it does not live on the sand or pebble areas (Kuwamura 1981). The populations increased in summer and autumn, but decreased in winter, sometimes nearly zero. About 0.9 individuals per 100 m2 have been recorded at rocky reefs at Shirahama (Kuwamura 1981).
It is common in the Capricorn/ Bunker Group, One Tree and Heron Islands and Wistari Reef, Fairfax, Fitzroy, Llewellyn and Musgrave Islands on the Great Barrier Reef, with 1.77 recruits per 100m2 (Eckert 1984).
In Australia, it was found to be one of the most abundant labrids at Lizard Island, GBR (three individuals per 150 m2) and occurred in similar densities in all habitat zones (Green 1996).
In Hong Kong, it is common in shallow areas of boulders and coral areas, but never abundant (Sadovy and Cornish 2000).
In Fiji, a total of 475 individuals were observed in various UVC surveys with body sizes of 4-17 cm TL (M. Kulbicki pers. comm. 2008).
In New Caledonia, a total of 1,407 individuals were observed in various UVC surveys with body sizes of 3-22 cm TL. In 31 stations, a total of 58 individuals were caught with a total weight of 242.1 g (M. Kulbicki pers. comm. 2008).
In French Polynesia, a total of 568 individuals were observed in various UVC surveys with body sizes of 4-12 cm TL (M. Kulbicki pers. comm. 2008)
In Tonga, a total of 205 individuals were observed in various UVC surveys with body sizes of 3-11 cm TL (M. Kulbicki pers. comm. 2008).
Mean density was 1.5 fish per 100 m2 on coral reefs of the Adang-ra Wi Islands in the Adaman Sea (Satapoomin undated).
It is common at Enewetak Atoll, Marshall Islands (Colin and Bell 1991), Solomon Islands (Allen 2006) and in the Red Sea (Richard and Field 1998).
In Pangkor Island, Malaysia an estimated mean density of 0.33 individuals from three 100 m X 2 m transects was recorded in underwater fish visual surveys (Y. Yusuf unpublished data).
On the east coast of Peninsular Malaysia, an estimated mean density of 4.55 individuals from twenty 50 m X 5 m transects was recorded in underwater fish visual surveys (Yusuf et al. 2002).
Population Trend
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Threats
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IUCN 2006 2006 IUCN red list of threatened species. www.iucnredlist.org. Downloaded July 2006.
http://www.fishbase.org/references/FBRefSummary.php?id=57073
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Management
Conservation Actions
This species has been observed at protected areas on the Great Barrier Reef, Australia (Hutchins and Sawinston 1996), at Ras Mohammed National Park, Egypt (Bshary 2003) and in the Mafia Island Marine Park, Tanzania (Garpe and Öhman 2003). Given the intensive collection of this species for the aquarium trade, more research is needed on the local and global impact of collection, as well as on the implementation of sustainable harvest and trade measures.
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Relevance to Humans and Ecosystems
Benefits
Importance
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Baensch, H.A. 1992 Neue Meerwasser-Praxis. Tetra Verlag, Melle, Germany. (Ref. 7309)
http://www.fishbase.org/references/FBRefSummary.php?id=7309&speccode=944
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Westneat, M.W. 2001 Labridae. Wrasses, hogfishes, razorfishes, corises, tuskfishes. p. 3381-3467. In K.E. Carpenter and V. Niem (eds.) FAO species identification guide for fishery purposes. The living marine resources of the Western Central Pacific. Vol. 6. Bony fishes part 4 (Labridae to Latimeriidae), estuarine crocodiles. FAO, Rome. (Ref. 9823)
http://www.fishbase.org/references/FBRefSummary.php?id=9823&speccode=4844
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Economic Importance for Humans: Negative
Wrasses are not known to have any negative affects on humans.
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Economic Importance for Humans: Positive
Cleaner wrasses benefit humans by increasing the survival of various economically important fish. They increase the survival of larger fish by eating and removing harmful parasites and diseased tissue from their scales and body.
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Wikipedia
Bluestreak cleaner wrasse
The bluestreak cleaner wrasse (Labroides dimidiatus) is one of several species of cleaner wrasse found on coral reefs in the Indian Ocean and much of the Pacific Ocean, as well as many seas, including the Red Sea and those around Southeast Asia. Like other cleaner wrasses, it eats parasites and dead tissue off larger fishes' skin in a mutualist relationship that provides food and protection for the wrasse, and considerable health benefits for the other fish.[1][2]
Behavior [edit]
Cleaner wrasses usually can be found around cleaning stations. The bigger fish recognise them as cleaner fish because they have a lateral stripe along the length of the body[3] and by their movement patterns. Upon recognising the cleaner and successfully soliciting its attention, client fish adopt a species specific pose to allow the cleaner access to its body surface, gills and sometimes mouth. A species of blenny called Aspidontus taeniatus has evolved this behavior as mimicry, in order to tear small pieces of flesh from bigger fish. Another species the bluestreak fangblenny, Plagiotremus rhinorhynchos, mimics juvenile cleaner wrasse so that its presence is tolerated by the cleaners and, it is assumed, can take advantage of the concentration of potential victims[4]
All cleaner wrasses start their lives as females. In a group of 6–8 cleaner wrasses there is only one male, the rest are females or juveniles. The strongest female changes its sex when the male dies, an occurrence known as sequential hermaphroditism.
Cleaner wrasses sleep in crevices between rocks or corals, covered in a slime layer that is secreted at dusk. In the morning these can be seen floating on the surface. They live about four years and can grow up to four inches.
References [edit]
- ^ Côté, I.M. (2000). "Evolution and ecology of cleaning symbioses in the sea". Oceanography and Marine Biology 38 (1): 311–355.
- ^ Johnsom, M.L. (2012). Biodiversity Sciences http://www.biodiversityscience.com/2012/01/31/high-street-cleaners/
|url=missing title (help). - ^ Stummer, L.E., Weller, J.A., Johnson, M.L., & Côté, I.M. (2005). "Size and stripes: how clients recognise cleaners". Animal Behaviour 68 (1): 145–150. doi:10.1016/j.anbehav.2003.10.018.
- ^ Johnson, Magnus and Hull, Susan (2006). "Interactions between fangblennies (Plagiotremus rhinorhynchos) and their potential victims: fooling the model rather than the client?". Marine Biology 148 (1): 889–897. doi:10.1007/s00227-005-0118-y.
Further reading [edit]
- Meulengracht-Madsen, Jens: (1976) Akvariefisk i farger, J.W. Cappelens forlag AS
- Labroides dimidiatus at FishBase
| Wikispecies has information related to: Labroides dimidiatus |
| Wikimedia Commons has media related to: Labroides dimidiatus |
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