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22 November 2019

Sarotherodon galilaeus (mango tilapia)

Publication: CABI Compendium
65484
Datasheet Types: Cultured aquatic species, Invasive species, Host animal

Abstract

This datasheet on Sarotherodon galilaeus covers Identity, Overview, Distribution, Dispersal, Biology & Ecology, Environmental Requirements, Impacts, Uses, Management, Genetics and Breeding, Further Information.

Identity

Preferred Scientific Name
Sarotherodon galilaeus Linnaeus, 1758
Preferred Common Name
mango tilapia
Other Scientific Names
Chromis galilaeus Linnaeus, 1758
Chromis lateralis Duméril, 1858
Chromis mircrostomus Lortet, 1883
Chromis pleuromelas Duméril, 1858
Chromis tiberiadis Lortet, 1883
Sarotherodon galilaeus Linnaeus, 1758
Sarotherodon galileus galilaeus Linnaeus, 1758
Tilapia galilaea Linnaeus, 1758
Tilapia galilaea galilaea Linnaeus, 1758
Tilapia galilaea pleuromelas Duméril, 1858
Tilapia lateralis Duméril, 1858
Tilapia macrocentra Duméril, 1858
Tilapia microstoma Lortet, 1883
Tilapia pleuromelas Duméril, 1858
International Common Names
English
St. Peter's fish
Local Common Names
Egypt
bolti nalawi
Germany
Prachtmaulbrüter
Israel
amnon hagalil
amnun galil
nusht abiad
Jordan
okkar
Nigeria
epia
garagaza
gargaza
ifunu
karwa
mpupa
tome
tsokungi
ukuobu
Russian Federation
tsikhlida
Senegal
wass
USA
St. Peter's fish

Pictures

Sarotherodon galilaeus (mango tilapia); adult, length 25cm. Upper Egypt, August 2010.
Adult
Sarotherodon galilaeus (mango tilapia); adult, length 25cm. Upper Egypt, August 2010.
©Magdy A. Saleh/via Fishbase (Image can be freely copied and altered, as long as original author and source are properly acknowledged)

Overview


Sarotherodon galilaeus galilaeus
like other tilapia species is of importance as a food fish. It is used for aquaculture and has been naturalized in many countries. S. galilaeus galilaeus has been listed in the IUCN Red List of as a vulnerable species (Stiassny, 1996).

Taxonomic Tree

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Description


Sarotherodon galilaeus galilaeus
has 14-17 dorsal spines, 13 dorsal soft rays, 3 anal spines, and 9-12 anal soft rays (FishBase, 2004). Melanin patches are found only in occasional individuals, and the caudal is naked except at the base. Reproductive individuals are greyish dorsally and silvery ventrally. Dorsal and caudal fins are with pinkish margins. Pectoral fins usually extend to above the vent or spinous anal fin. Males have longer soft dorsal and anal fin rays.

Pathogens Carried

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Distribution


Sarotherodon galilaeus galilaeus
is found in Africa and Eurasia. It is distributed in: the Jordan system especially in lakes, the coastal rivers of Israel, the Nile system including the delta lakes and Lake Albert and Turkana, Jebel Mara, the Chad Basin, the Shari River, the Central Congo Basin, the Ubanghi and Uele Rivers, Lake Kotto, the Niger, Ogun, Volta, Corubal, Gambia, Casamance and Senegal Rivers, Draa (Morocco) and Adrar (Mauritania) (FishBase, 2004). Populations in Lake Ejagham, Cameroon are vulnerable (Baillie and Groombridge, 1996).

Distribution Map

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Distribution Table

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Introductions

Introduced toIntroduced fromYearReasonsIntroduced byEstablished in wild throughReferencesNotes
Natural reproductionContinuous restocking
ChinaAfrica1981
Unknown
NoNo 
CongoSudan1953
International organisation
YesNo 
JapanUSA1964
Unknown
NoNo
Chiba and et al. (1989)
 
South AfricaIsrael1959
Unknown
NoNo 

Anatomy


Sarotherodon galilaeus galilaeus
have fine teeth and are microphagous and omnivorous.

Habitat List

CategorySub categoryHabitatPresenceStatus
Freshwater    
Brackish    

Climate

Climate typeDescriptionPreferred or toleratedRemarks
A - Tropical/Megathermal climateAverage temp. of coolest month > 18°C, > 1500mm precipitation annuallyPreferred 

Air Temperature

ParameterLower limit (°C)Upper limit (°C)
Mean annual temperature2228

Water Tolerances

ParameterMinimum valueMaximum valueTypical valueStatusLife stageNotes
Bicarbonate (mg/l)  28OptimumBroodstock 
Dissolved oxygen (mg/l)  <3.0HarmfulAdult 
Dissolved oxygen (mg/l)  <3.0HarmfulFry 
Dissolved oxygen (mg/l)  >0.5OptimumFry 
Dissolved oxygen (mg/l)  >5.0OptimumAdult 
Dissolved oxygen (mg/l)  >5.0OptimumLarval 
Hardness (mg/l of Calcium Carbonate)6 dH15 dH OptimumAdult 
Water pH (pH)68 OptimumAdult 
Water pH (pH)7.07.5 OptimumBroodstock 
Water pH (pH)7.07.5 OptimumLarval 
Water pH (pH)7.07.5 OptimumFry 
Water temperature (ºC temperature)2228 OptimumAdult 

List of Diseases and Disorders

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Impact Summary

CategoryImpact
Fisheries / aquaculturePositive

Uses List

Human food and beverage > Fresh meat
Human food and beverage > Frozen meat
Human food and beverage > Whole

Behaviour


Sarotherodon galilaeus galilaeus
is known to occur at temperatures as low as 9°C (Trewavas, 1983.). It is known to forms schools occasionally and are territorial in behaviour. It prefers open waters but juveniles and breeding adults are found inshore (Trewavas and Teugels, 1991). It often associated with beds of submerged vegetation in Sudd lakes. It feeds on algae and fine organic debris.
S. galilaeus galilaeus broods the eggs and the larvae in the mouth and known as a bi-parental mouth brooder (Bailey, 1994). The initiative throughout courting and mating is taken predominantly by the female. The female is mainly responsible for the excavation of nest and defending mating territory. Pair-formation exists and is dissolved as soon as the eggs are in the parental mouth (FishBase, 2004).

Reproduction

Unmanaged ponds are the most widely used hatchery system. Ponds require low input and management but also result in low production. Net enclosures, tanks and ponds are used as hatchery systems for propagation. Net enclosures are usually made of fine nylon, plastic mosquito netting or cotton mesh. Net enclosures or ‘hapas’ can be any manageable size from 1-40 m² with a depth of 1-2 m. Spawning units in a tank system are usually circular tanks of 1-6 m diameter containing 0.5-0.7 m of water.

Growout Management Table

Growout Management

Growout production systems practised in Sarotherodon galilaeus galilaeus culture are ponds, cages, tanks and rice fields. Different types of ponds are used for culture of S. galilaeus galilaeus. The most widespread but most unproductive are low input ponds with uncontrolled breeding and irregular harvesting. Higher yields are achieved by employing monosex fish for stocking in fertilized well-managed ponds. The advantage of using cages and tanks for culture is avoidance of overbreeding. Intensive culture is more common in tanks and cages.

Seed Supply and Species Availability


Sarotherodon galilaeus galilaeus
fry and fingerling stages are used to stock aquaculture ponds. Fry are produced in hatchery systems.

Reproduction and Seed Production Systems

Reproduction Conditions
ParameterValueRemarks
FertilizationExternal1 
Reproductive guildGuarders1 
Reproductive guildExternal - Bearers1 
Broodstock Conditions
ParameterValueRemarks
BreedingNaturalyes 
ModeAssistedyes 
ModeUnassistedyes 
Culture system Stocking densityExtensiveyes 
Culture system Stocking densitySemi-intensiveyes 
Culture system Stocking densityIntensiveyes 
Sex ratio male/femaleSex ratio male/female1:2-7 
Egg production/kgEgg production/kg (/female)600-2000 
Egg Nursery Conditions
Egg Nursery Conditions
ParameterValueRemarks
Culture system Stocking densityExtensiveyes 
Egg ProductionTime to hatch (hours)96 
Larval Nursery Conditions
ParameterValueRemarks
Culture system Stocking densityExtensiveyes 
Larval ProductionTime to fry (days)12 
Larval ProductionFirst feed (days)9-12 
Fry Nursery Conditions
ParameterValueRemarks
Culture system Stocking densityExtensiveyes 
Culture system Stocking densitySemi-intensiveyes 
Culture system Stocking densityIntensiveyes 

Natural Food Sources

Food sourceLife stagesContribution to total food intake (%)Feeding methodsFeeding frequencyFeeding characteristicsDetails
benthic algae/weeds      
detritus
Aquatic|Adult
Aquatic|Fry
54-70    
periphyton
Aquatic|Adult
Aquatic|Fry
     
phytoplankton
Aquatic|Adult
Aquatic|Fry
     
zoobenthos
Aquatic|Adult
Aquatic|Fry
     
zooplankton
Aquatic|Adult
Aquatic|Fry
     

Genetics Table

CountryLocalityHaploidDiploidMarkersReferences
  2244y
Klinkhardt and et al. (1995)
  2244n
Klinkhardt and et al. (1995)
  2244y
IsraelSea of Galilee 44n 

Electrophoretic Studies

CountryLocalityTotal lociObservedExpectedPolymorphic lociReferences
Côte d'IvoireComoé, Abengourou240.0000.0000.000
KenyaLake Turkana220.0430.04620.136

Links to Websites

NameURLComment
GISD/IASPMR: Invasive Alien Species Pathway Management Resource and DAISIE European Invasive Alien Species Gatewayhttps://doi.org/10.5061/dryad.m93f6Data source for updated system data added to species habitat list.
Global register of Introduced and Invasive species (GRIIS)http://griis.org/Data source for updated system data added to species habitat list.

References

Arkhipchuk VV, 1999. Chromosome database. Database of Dr. Victor Arkhipchuk. Ukraine.
Bailey RG, 1994. Guide to the fishes of the River Nile in the Republic of the Sudan. J. Nat. Hist., 28:937-970.
Baillie J, Groombridge B, eds, 1996. 1996 IUCN red list of threatened animals. Gland, Switzerland: IUCN, 378 pp.
Chiba K, Taki Y Sakai K, Oozeki Y, 1989. Present status of aquatic organisms introduced into Japan. In: De Silva SS, ed., Exotic aquatic organisms in Asia, Proceedings of the Workshop on Introduction of Exotic Aquatic Organisms in Asia, p 63-70, Asian Fish Soc. Spec. Publ. 3,. Manila, Philippines: Asian Fish Society.
FAO, 1997. FAO Database on Introduced Aquatic Species. FAO, Rome, Italy: Food and Agricultural Organization of the United Nations.
FishBase, 2004. Entry for Sarotherodon galilaeus galilaeus. Main ref. Trewavas E, 1983. Tilapiine fishes of the genera Sarotherodon, Oreochromis and Danakilia. London, UK: British Mus. Nat. Hist., 583 pp. Online at www.fishbase.org. Accessed 10 May 2004.
Johnson RP, 1974. Synopsis of biological data on Sarotherodon galilaeus. FAO Fish. Synop. (90), 42 pp.
Klinkhardt M, Tesche M, Greven H, 1995. Database of fish chromosomes. Westarp Wissenschaften, 179 pp.
Kornfield I, 1984. Descriptive genetics of cichlid fishes. In: Turner BJ, ed. Evolutionary genetics of fishes. New York: Plenum Publishing Corporation, 591-616.
McAndrew BJ, Majumdar KC, 1983. Tilapia stock identification using electrophoretic markers. Aquaculture, 30(1/4):249-261.
Paugy D, Traoré K, Diouf PS, 1994. Faune ichtyologique des eaux douces d’Afrique de l’Ouest. In: Teugels GG, Guégan JF, Albaret JJ, eds. Biological diversity of African fresh- and brackish water fishes. Geographical overviews presented at the PARADI Symposium, Senegal, 15-20 November 1993. Ann. Mus. R. Afr. Centr., Sci. Zool., 275:35-66.
Stiassny M, 1996. Sarotherodon galileus ssp. "Ejagham" nom. prov. 2003 IUCN Red List of Threatened Species. Online at www.redlist.org/search/details.php?species=19912. Accessed on 25 May 2004.
Teugels GG, Lévêque C, Paugy D, Traoré K, 1988. État des connaissances sur la faune ichtyologique des bassins côtiers de Côte d’Ivoire et de l’ouest du Ghana. Rev. Hydrobiol. Trop., 21(3):221-237.
Trewavas E, 1983. Tilapiine fishes of the genera Sarotherodon, Oreochromis and Danakilia. London, UK: British Museum of Natural History, 583 pp.
Trewavas E, Teugels GG, 1991. Sarotherodon. In: Daget J, Gosse J-P, Teugels GG, Thys van den Audenaerde DFE, eds. Check-list of the freshwater fishes of Africa (CLOFFA). ISNB, Brussels; MRAC, Tervuren; and ORSTOM, Paris. Vol. 4, 425-437.
Welcomme RL, 1988. International introductions of inland aquatic species. FAO Fisheries Technical Paper, No. 294:x + 318 pp.

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Published online: 22 November 2019

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