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Mozambique tilapia

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Mozambique tilapia
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Actinopterygii
Order: Cichliformes
Family: Cichlidae
Genus: Oreochromis
Species:
O. mossambicus
Binomial name
Oreochromis mossambicus
Synonyms
  • Chromis mossambicus W. K. H. Peters, 1852
  • Chromis niloticus var. mossambicus W. K. H. Peters, 1852
  • Sarotherodon mossambicus (W. K. H. Peters, 1852)
  • Tilapia mossambica (W. K. H. Peters, 1852)
  • Tilapia mossambica mossambica (W. K. H. Peters, 1852)
  • Tilapia mossambicus (W. K. H. Peters, 1852)
  • Chromis dumerilii Steindachner, 1864
  • Tilapia dumerilii (Steindachner, 1864)
  • Chromis vorax Pfeffer, 1893
  • Tilapia vorax (Pfeffer, 1893)
  • Chromis natalensis M. C. W. Weber, 1897
  • Sarotherodon mossambicus natalensis (M. C. W. Weber, 1897)
  • Tilapia natalensis (M. C. W. Weber, 1897)
  • Tilapia arnoldi Gilchrist & W. W. Thompson, 1917
  • Oreochromis mossambicus bassamkhalafi Khalaf, 2009

The Mozambique tilapia (Oreochromis mossambicus) is an oreochromine cichlid fish native to southeastern Africa. Dull colored, the Mozambique tilapia often lives up to a decade in its native habitats. It is a popular fish for aquaculture. Due to human introductions, it is now found in many tropical and subtropical habitats around the globe, where it can become an invasive species because of its robust nature. These same features make it a good species for aquaculture because it readily adapts to new situations. It is known as black tilapia in Colombia[2] and as blue kurper in South Africa.[3]

Description

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The native Mozambique tilapia is laterally compressed, and has a deep body with long dorsal fins, the front part of which have spines. Native coloration is a dull greenish or yellowish, and weak banding may be seen. Adults reach up to 39 cm (15 in) in standard length and up to 1.1 kg (2.4 lb).[4] Size and coloration may vary in captive and naturalized populations due to environmental and breeding pressures. It lives up to 11 years.[4]

Distribution and habitat

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An adult male in breeding condition

The Mozambique tilapia is native to inland and coastal waters in southeastern Africa, from the Zambezi basin in Mozambique, Malawi, Zambia and Zimbabwe to Bushman River in South Africa's Eastern Cape province.[1][5] It is threatened in its home range by the introduced Nile tilapia. In addition to competing for the same resources, the two readily hybridize.[1][6] This has already been documented from the Zambezi and Limpopo Rivers, and it is expected that pure Mozambique tilapia eventually will disappear from both.[1]

Otherwise it is a remarkably robust and fecund fish, readily adapting to available food sources and breeding under suboptimal conditions. Among others, it occurs in rivers, streams, canals, ponds, lakes, swamps and estuaries, although it typically avoids fast-flowing waters, waters at high altitudes and the open sea.[1][4] It inhabits waters that range from 17 to 35 °C (63–95 °F).[4][7]

Invasiveness

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Mozambique tilapia from West Bengal, India.

The Mozambique tilapia or hybrids involving this species and other tilapia are invasive in many parts of the world outside their native range, having escaped from aquaculture or been deliberately introduced to control mosquitoes.[8] The Mozambique tilapia has been nominated by the Invasive Species Specialist Group as one of the 100 worst invasive species in the world.[9] It can harm native fish populations through competition for food and nesting space, as well as by directly consuming small fish.[10] In Hawaii, striped mullet Mugil cephalus are threatened because of the introduction of this species. The population of hybrid Mozambique tilapia x Wami tilapia in California's Salton Sea may also be responsible for the decline of the desert pupfish, Cyprinodon macularius.[11][12][13]

Hybridization

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As with most species of tilapia, Mozambique tilapia have a high potential for hybridization. They are often crossbred with other tilapia species in aquaculture because purebred Mozambique tilapia grow slowly and have a body shape poorly suited to cutting large fillets. However, Mozambique tilapia have the desirable trait of being especially tolerant of salty water.[14] Also, hybrids between certain parent combinations (such as between Mozambique and Wami tilapia) result in offspring that are all or predominantly male. Male tilapia are preferred in aquaculture as they grow faster and have a more uniform adult size than females. The "Florida Red" tilapia is a popular commercial hybrid of Mozambique and blue tilapia.[15]

Behavior

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Feeding

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Mozambique tilapia are omnivorous. They can consume detritus, diatoms, phytoplankton,[16] invertebrates, small fry and vegetation ranging from macroalgae to rooted plants.[17][18] This broad diet helps the species thrive in diverse locations.

Due to their robust nature, Mozambique tilapias often over-colonize the habitat around them, eventually becoming the most abundant species in a particular area. When over-crowding happens and resources get scarce, adults will sometimes cannibalize the young for more nutrients. Mozambique tilapia, like other fish such as Nile tilapia and trout, are opportunistic omnivores and will feed on algae, plant matter, organic particles, small invertebrates and other fish.[19] Feeding patterns vary depending on which food source is the most abundant and the most accessible at the time. In captivity, Mozambique tilapias have been known to learn how to feed themselves using demand feeders. During commercial feeding, the fish may energetically jump out of the water for food.[16]

Social structure

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Mozambique tilapias often travel in groups where a strict dominance hierarchy is maintained. Positions within the hierarchy correlate with territoriality, courtship rate, nest size, aggression, and hormone production.[20] In terms of social structure, Mozambique tilapias engage in a system known as lek-breeding, where males establish territories with dominance hierarchies while females travel between them. Social hierarchies typically develop because of competition for limited resources including food, territories, or mates. During the breeding season, males cluster around certain territory, forming a dense aggregation in shallow water.[21] This aggregation forms the basis of the lek through which the females preferentially choose their mates. Reproductive success by males within the lek is highly correlated to social status and dominance.[22]

In experiments with captive tilapias, evidence demonstrates the formation of linear hierarchies where the alpha male participates in significantly more agonistic interactions. Thus, males that are higher ranked initiate much more aggressive acts than subordinate males. However, contrary to popular belief, Mozambique tilapias display more agonistic interactions towards fish that are farther apart in the hierarchy scale than they do towards individuals closer in rank. One hypothesis behind this action rests with the fact that aggressive actions are costly. In this context, members of this social system tend to avoid confrontations with neighboring ranks in order to conserve resources rather than engage in an unclear and risky fight. Instead, dominant individuals seek to bully subordinate tilapias both for an easy fight and to keep their rank.[23]

Communication and aggression

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Urine in Mozambique tilapias, like many freshwater fish species, acts as a vector for communication amongst individuals. Hormones and pheromones released with urine by the fish often affect the behavior and physiology of the opposite sex. Dominant males signal females through the use of a urinary odorant. Further studies have suggested that females respond to the ratio of chemicals within the urine, as opposed to the odor itself. Nevertheless, females are known to be able to distinguish between hierarchical rank and dominant vs. subordinate males through chemicals in urine.

Urinary pheromones also play a part in male – male interaction for Mozambique tilapias. Studies have shown that male aggression is highly correlated with increased urination. Symmetrical aggression between males resulted in an increase in the release of urination frequency. Dominant males both store and release more potent urine during agonistic interactions. Thus, both the initial stage of lek formation and the maintenance of social hierarchy may highly depend on the males’ varying urinary output.[24]

Aggression amongst males usually involve a typical sequence of visual, acoustic, and tactile signals that eventually escalates to physical confrontation if no resolution is reached. Usually, conflict ends before physical aggression as fights are both costly and risky. Bodily damage may impede an individual's ability to find a mate in the future. In order to prevent cheating, in which individual may fake his own fitness, these aggressive rituals incur significant energetic costs. Thus, cheating is prevented by the sheer fact that the costs of initiating a ritual often outweigh the benefits of cheating. In this regard, differences between individuals in endurance plays a critical role in resolving the winner and the loser.[25]

Reproduction

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In the first step in the reproductive cycle for Mozambique tilapia, males excavate a nest into which a female can lay her eggs. After the eggs are laid, the male fertilizes them. Then the female stores the eggs in her mouth until the fry hatch; this act is called mouthbrooding.[26] One of the main reasons behind the aggressive actions of Mozambique tilapias is access to reproductive mates. The designation of Mozambique tilapias as an invasive species rests on their life-history traits: Tilapias exhibit high levels of parental care as well as the capacity to spawn multiple broods through an extended reproductive season, both contributing to their success in varying environments.[27] In the lek system, males congregate and display themselves to attract females for matings. Thus, mating success is highly skewed towards dominant males, who tend to be larger, more aggressive, and more effective at defending territories. Dominant males also build larger nests for the spawn.[21] During courtship rituals, acoustic communication is widely used by the males to attract females. Studies have shown that females are attracted to dominant males who produce lower peak frequencies as well as higher pulse rates. At the end of mating, males guard the nest while females take both the eggs and the sperm into their mouth. Due to this, Mozambique tilapias can occupy many niches during spawning since the young can be transported in the mouth.[28] These proficient reproductive strategies may be the cause behind their invasive tendencies.

Male Mozambique tilapias synchronize breeding behavior in terms of courtship activity and territoriality in order to take advantage of female spawning synchrony. One of the costs associated with this synchronization is the increase in competition among males, which are already high on the dominance hierarchy. As a result, different mating tactics have evolved in these species. Males may mimic females and sneak reproduction attempts when the dominant male is occupied. Likewise, another strategy for males is to exist as a floater, travelling between territories in an attempt to find a mate. Nevertheless, it is the dominant males who have the greatest reproductive advantage.[29]

Parental care

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Typically, Mozambique tilapias, like all species belonging to the genus Oreochromis and species like Astatotilapia burtoni, are maternal mouthbrooders, meaning that spawn is incubated and raised in the mouth of the mother. Parental care is, therefore, almost exclusive to the female. Males do contribute by providing nests for the spawn before incubation, but the energy costs associated with nest production is low relative to mouthbrooding. Compared to nonmouthbrooders, both mouthbrooding and growing a new clutch of eggs is not energetically feasible. Thus, Mozambique tilapias arrest oocyte growth during mouthbrooding to conserve energy.[30] Even with oocyte arrest, females that mouthbrood take significant costs in body weight, energy, and low fitness. Hence, parental-offspring conflict is visible through the costs and benefits to the parents and the young. A mother caring for her offspring carries the cost of reducing her own individual fitness. Unlike most fish, Mozambique tilapias exhibit an extended maternal care period believed to allow social bonds to be formed.[31]

Use in aquaculture

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An albino strain has been developed in captivity
Capture (blue) and aquaculture (green) production of Mozambique tilapia (Oreochromis mossambicus) in thousand tonnes from 1950 to 2022, as reported by the FAO[32]

Mozambique tilapia are hardy individuals that are easy to raise and harvest, making them a good aquacultural species. They have a mild, white flesh that is appealing to consumers. This species constitutes about 4% of the total tilapia aquaculture production worldwide, but is more commonly hybridized with other tilapia species.[33] Tilapia are very susceptible to diseases such as whirling disease and ich.[26] Mozambique tilapia are resistant to wide varieties of water quality issues and pollution levels. Because of these abilities they have been used as bioassay organisms to generate metal toxicity data for risk assessments of local freshwater species in South Africa rivers.[34]

Mozambique tilapia were one of the species flown on the Bion-M No.1 spacecraft in 2013, but they all died due to equipment failure.[35]

Other names

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The species is known by a number of other names including:

  • Mujair in Indonesia, the name derived from a Javanese breeder Moedjair.
  • Daya in Pakistan
  • Jesus fish in the Elim area of Jamaica, named for their habit of multiplying [36]

References

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  1. ^ a b c d e Bills, R. (2019). "Oreochromis mossambicus". IUCN Red List of Threatened Species. 2019: e.T63338A174782954. doi:10.2305/IUCN.UK.2019-3.RLTS.T63338A174782954.en. Retrieved 19 November 2021.
  2. ^ "Listado oficial de especies invasoras para Colombia | Parques Nacionales Naturales de Colombia".
  3. ^ "Big Bass". Archived from the original on 2019-06-14. Retrieved 2012-03-22.
  4. ^ a b c d Froese, Rainer; Pauly, Daniel (eds.). "Oreochromis mossambicus". FishBase. September 2019 version.
  5. ^ "GISD". Archived from the original on 2012-09-27. Retrieved 2010-09-12.
  6. ^ Waal 2002
  7. ^ Ford, A.G.P.; et al. (2019). "Molecular phylogeny of Oreochromis (Cichlidae: Oreochromini) reveals mito-nuclear discordance and multiple colonisation of adverse aquatic environments" (PDF). Mol. Phylogenet. Evol. 136: 215–226. doi:10.1016/j.ympev.2019.04.008. PMID 30974200. S2CID 109938635.
  8. ^ Moyle 1976
  9. ^ Courtenay 1989
  10. ^ Courtenay et al. 1974
  11. ^ Courtenay and Robins 1989
  12. ^ Swift et al. 1993
  13. ^ Riedel, R.; B.A. Costa-Pierce (2002). "Review of the Fisheries of the Salton Sea, California, USA: Past, Present, and Future". Reviews in Fisheries Science. 10 (2): 77–112. doi:10.1080/20026491051686. S2CID 214614676.
  14. ^ Wan, Z.Y.; G. Lin; G. Yue (2019). "Genes for sexual body size dimorphism in hybrid tilapia (Oreochromis sp. x Oreochromis mossambicus)". Aquaculture and Fisheries. 4 (6): 231–238. doi:10.1016/j.aaf.2019.05.003. hdl:10356/142831.
  15. ^ "Culture of Hybrid Tilapia: A Reference Profile". 2018-11-21.
  16. ^ a b De Peaza, Mia. "Oreochromis mossambicus (Mozambique Tilapia)" (PDF). The Online Guide to the Animals of Trinidad and Tobago. UWI. Retrieved 24 October 2013.
  17. ^ Mook 1983
  18. ^ Trewevas 1983
  19. ^ "Biology and ecology of Mozambique tilapia (Oreochromis mossambicus)" (PDF). feral.org.au. Archived from the original (PDF) on 29 October 2013. Retrieved 24 October 2013.
  20. ^ Oliveira, Rui F.; Vitor C. Almada; Adelino V. M. Canario (1996). "Social Modulation of Sex Steroid Concentrations in the Urine of Male Cichlid Fish Oreochromis mossambicus". Hormones and Behavior. 30 (1): 2–12. doi:10.1006/hbeh.1996.0002. hdl:10400.1/3206. PMID 8724173. S2CID 1951640.
  21. ^ a b Amorim, M. Clara P.; Almada, Vitor C. (1 March 2005). "The outcome of male–male encounters affects subsequent sound production during courtship in the cichlid fish Oreochromis mossambicus". Animal Behaviour. 69 (3): 595–601. doi:10.1016/j.anbehav.2004.06.016. hdl:10400.12/1440. S2CID 34065315.
  22. ^ Barata, Eduardo N.; Fine, Jared M.; Hubbard, Peter C.; Almeida, Olinda G.; Frade, Pedro; Sorensen, Peter W.; Canário, Adelino V. M. (1 April 2008). "A Sterol-Like Odorant in the Urine of Mozambique Tilapia Males Likely Signals Social Dominance to Females". Journal of Chemical Ecology. 34 (4): 438–449. doi:10.1007/s10886-008-9458-7. PMID 18379847. S2CID 33463442.
  23. ^ Oliveira, R.F.; V.C. Almada (1996). "Dominance hierarchies and social structure in captive groups of the Mozambique tilapia Oreochromis mossambicus (Teleostei Cichlidae)". Ethology Ecology & Evolution. 8: 39–55. doi:10.1080/08927014.1996.9522934. hdl:10400.12/1330.
  24. ^ Barata, Eduardo N; Hubbard, Peter C; Almeida, Olinda G; Miranda, António; Canário, Adelino VM (1 January 2007). "Male urine signals social rank in the Mozambique tilapia (Oreochromis mossambicus)". BMC Biology. 5 (1): 54. doi:10.1186/1741-7007-5-54. PMC 2222621. PMID 18076759.
  25. ^ Ros, Albert F.H.; Klaus Becker; Rui F. Oliveira (30 May 2006). "Aggressive behaviour and energy metabolism in a cichlid fish, Oreochromis mossambicus". Physiology & Behavior. 89 (2): 164–70. doi:10.1016/j.physbeh.2006.05.043. hdl:10400.12/1299. PMID 16828128. S2CID 920011.
  26. ^ a b Popma, 1999
  27. ^ Russell, D. J.; Thuesen, P. A.; Thomson, F. E. (1 May 2012). "Reproductive strategies of two invasive tilapia species Oreochromis mossambicus and Tilapia mariae in northern Australia". Journal of Fish Biology. 80 (6): 2176–2197. Bibcode:2012JFBio..80.2176R. doi:10.1111/j.1095-8649.2012.03267.x. PMID 22551176.
  28. ^ Amorim, M. C. P.; Fonseca, P. J.; Almada, V. C. (1 March 2003). "Sound production during courtship and spawning of Oreochromis mossambicus: male-female and male-male interactions" (PDF). Journal of Fish Biology. 62 (3): 658–672. Bibcode:2003JFBio..62..658A. doi:10.1046/j.1095-8649.2003.00054.x. hdl:10400.12/1452. S2CID 28236698. Archived from the original (PDF) on 4 February 2021.
  29. ^ Oliveira, R. F.; Almada, V. C. (1 June 1998). "Mating tactics and male-male courtship in the lek-breeding cichlid Oreochromis mossambicus". Journal of Fish Biology. 52 (6): 1115–1129. doi:10.1111/j.1095-8649.1998.tb00959.x. hdl:10400.12/1340.
  30. ^ Smith, Carol Johnson; Haley, Samuel R. (1 January 1988). "Steroid profiles of the female tilapia, Oreochromis mossambicus, and correlation with oocyte growth and mouthbrooding behavior". General and Comparative Endocrinology. 69 (1): 88–98. doi:10.1016/0016-6480(88)90056-1. PMID 3360291.
  31. ^ Russock, Howard I. (March 1986). "Preferential Behaviour of Sarotherodon (Oreochromis) mossambicus (Pisces: Cichlidae) Fry to Maternal Models and Its Relevance to the Concept of Imprinting". Behaviour. 96 (3/4): 304–321. doi:10.1163/156853986x00531.
  32. ^ "Fisheries and Aquaculture - Global Production". Food and Agriculture Organization of the United Nations (FAO). Retrieved 2024-05-06.
  33. ^ Gupta and Acosta 2004
  34. ^ Mashifane, TB; Moyo, NAG (29 October 2014). "Acute toxicity of selected heavy metals to Oreochromis mossambicus fry and fingerlings". African Journal of Aquatic Science. 39 (3): 279–285. doi:10.2989/16085914.2014.960358. S2CID 85396607.
  35. ^ Zak, Anatoly. "Bion (12KSM) satellite". RussianSpaceWeb.com. Archived from the original on 9 June 2013. Retrieved 20 May 2013.
  36. ^ Fishbase.org

References

[edit]
  • "Oreochromis mossambicus". Integrated Taxonomic Information System. Retrieved 10 January 2007.
  • Courtenay W.R. Jr. 1989. Exotic fishes in the National Park System. Pages 237–252 in: Thomas L.K. (ed.). Proceedings of the 1986 conference on science in the national parks, volume 5. Management of exotic species in natural communities. U.S. National Park Service and George Wright Society, Washington, D.C.
  • Courtenay W.R. Jr., and C.R. Robins. 1989. Fish introductions: Good management, mismanagement, or no management? CRC Critical Reviews in Aquatic Sciences 1:159–172.
  • Courtenay, W.R. Jr.; Sahlman, H.F; Miley, W.W. II; Herrema, D.J. (1974). "Exotic fishes in fresh and brackish waters of Florida". Biological Conservation. 6 (4): 292–302. doi:10.1016/0006-3207(74)90008-1.
  • Gupta M.V. and B.O. Acosta. 2004. A review of global tilapia farming practices. WorldFish Center P.O. Box 500 GPO, 10670, Penang, Malaysia.
  • Mook, D (1983). "Responses of common fouling organisms in the Indian River, Florida, to various predation and disturbance intensities". Estuaries. 6 (4): 372–379. doi:10.2307/1351396. JSTOR 1351396. S2CID 87151335.
  • Moyle P.B. 1976. Inland fishes of California. University of California Press, Berkeley, CA. 330 p.
  • Popma, T. Tilapia Life History and Biology 1999 Southern Region Aquaculture Center
  • Swift, C.C.; Haglund, T.R.; Ruiz, M.; Fisher, R.N. (1993). "The status and distribution of the freshwater fishes of southern California". Bulletin of the Southern California Academy of Sciences. 92: 101–167.
  • Trewevas E. 1983. Tilapiine Fishes Of The Genera Sarotherodon, Oreochromis And Danakilia. British Museum Of Natural History, Publication Number 878.Comstock Publishing Associates. Ithaca, New York. 583 p.
  • Waal, Ben van der, 2002. Another fish on its way to extinction?. Science in Africa.
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