Growth, Mortality and Exploitation Levels of Sphyraena sphyraena (Pisces: Sphyraenidae) and Apsilus fuscus (Pisces: Lutjanidae) in Ghanaian Waters
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Sphyraena sphyraena (Linnaeus, 1758) and Apsilus fuscus (Valenciennes, 1830) are commercially important fish species in Ghana. The stocks are exploited mainly by the artisanal and semi-industrial fisheries. Growth and mortality rates, and exploitation levels of the two stocks in inshore waters of Ghana were assessed as a contribution to fill the knowledge gap on the species. Samples were obtained from three landing sites along the coast of Ghana from February to July, 2017. Length-frequency data were used to estimate growth, mortality and exploitation ratios. The modal class for S. sphyraena was 37.0–39.9 cm total length (TL) and 34.0–35.9 cm TL for A. fuscus. The length and weight relationships established that growth in S. sphyraena was negative allometric, whereas that of A. fuscus was isometric. The estimated growth parameters from the length frequency data fitted with the von Bertalanffy growth function were asymptotic length (L∞) of 69.9 cm TL for S. sphyraena and 53.5 cm TL for A. fuscus. The growth constant (K) was calculated as 1.64 yr-1 for S. sphyraena and 0.50 yr-1 for A. fuscus. The mean length-at-first capture (Lc) was found to be lower than the mean length at sexual maturity (Lm) for both species. The sex ratio showed a dominance of females over males in S. sphyraena, and 1:1 for A. fuscus. The total mortality rate (Z) for S. sphyraena was more than for A. fuscus. The estimated natural mortality (M) was 1.88 yr-1 for S. sphyraena and 0.74 yr-1 for A. fuscus whilst fishing mortality (F) rate was 3.04 yr-1 for S. sphyraena and 0.93 yr-1 for A. fuscus. The exploitation ratio showed that both fish stocks were exploited over the optimum levels. The estimated population parameters of the species obtained from the study, therefore, might be useful for the sustainable management of the stocks.
References
-
Ayivi, S. S. A. (2012). Seasonal trend and abundance of Sparids in Ghanaian coastal waters: An assessment of the artisanal fisheries sector (Final project, United Nations University). pp. 1–30. Retrieved from http://www.unuftp.is/static/fellows/document/sylvia11prf.pd.
Google Scholar
1
-
Koranteng, K. A. (2001). Structure and dynamics of demersal assemblages on the continental shelf and upper slope off Ghana, West Africa. Marine Ecology Progress Series, 220, 1-12. Retrieved from http://www.jstor.org/stable/24864838.
Google Scholar
2
-
Nunoo, F. K. E., Asiedu, B., Amador, K., Belhabib, D., & Pauly, D. (2014). Reconstruction of marine fisheries catches for Ghana, 1950–2010. Vancouver (Canada): Fisheries Centre, University of British Columbia.
Google Scholar
3
-
Bannerman, P. & Cowx, I.G. (2002). Stock Assessment of the big-eye grunt (Brachydeuterus auritus) fishery in Ghanaian Coastal Waters. Fisheries Research 59, 197-207.
Google Scholar
4
-
Aggrey-Fynn J., Fynn-Korsah S. & Appiah, N. (2013). Length-weight relationships and food preference of two coastal marine fishes, Galeiodes decadactylus (Polynemidae) and Sphyraena sphyraena (Sphyraenidae) off Cape Coast, Ghana. West African Journal of Applied Ecology. 21(1): 87-96.
Google Scholar
5
-
Palomera, I., Olivar, M. P., Salat, J., Sabatés, A., Coll, M., Garcıa, A., & Morales-Nin, B. (2007). Small pelagic fish in the NW Mediterranean Sea: An ecological review. Progress in Oceanography, 74, 377-396.
Google Scholar
6
-
Afonso, P., Porteiro, F. M., Santos, R. S., Barreiros, J. P., Worms, J., & Wirtz, P. (1999). Coastal marine fishes of São Tomé Island (Gulf of Guinea). Life and Marine Sciences 17(A), 65-92.
Google Scholar
7
-
Aggrey-Fynn, J., & Sackey-Mensah, R. (2012). Species diversity and relative abundance of fisheries resources found in beach seine along the central coast of Ghana. West African Journal of Applied Ecology, 20(1), 1-9.
Google Scholar
8
-
Belhabib, D., & Pauly, D. (2015). Fisheries Catch Reconstructions: West Africa: Part II [R]. Fisheries Centre Research Reports, 23, (3). doi: 10.14288/1.0354314.
Google Scholar
9
-
Belhabib, D., Ramdeen, S., & Pauly, D. (2015). An attempt at reconstructing the marine fisheries catches in the Congo (Ex-Zaïre), 1950-2010. Fisheries catch reconstructions: West Africa, Part II.
Google Scholar
10
-
Schneider, W. (1990). Field guide to the commercial marine resources of the Gulf of Guinea. FAO species identification sheets for fishery purposes.
Google Scholar
11
-
Stevens, M. H., Smith, S. G., & Ault, J. S. (2019). Life history demographic parameter synthesis for exploited Florida and Caribbean coral reef fishes. Fish and Fisheries, 20(6), 1196-1217.
Google Scholar
12
-
de Morais, L., Sagna, A., Nunoo, F., Camara, K., Carpenter, K.E., Djiman, R., … Quartey, R. (2015). Apsilus fuscus. The IUCN Red List of Threatened Species 2015: e.T194364A2322498. http://dx.doi.org/10.2305/IUCN.UK.2015-4.RLTS.T194364A2322498.en.
Google Scholar
13
-
Najmudeen, T. M., Seetha, P. K., & Zacharia, P. U. (2015). Fishery and population dynamics of the obtuse barracuda Sphyraena obtusata (Cuvier) landed by trawlers at Cochin, south-west coast of India. Indian Journal of Fisheries, 62(2), 14-18.
Google Scholar
14
-
Aheto, D., Asare, N., Quaynor, B., Tenkorang, E., Asare, C., & Okyere, I. (2015). Profitability of small-scale fisheries in Elmina, Ghana. Sustainability, 4(11): 2785-2794.
Google Scholar
15
-
Mensah, M. A., Korateng, K. A., Bortey, A., & Yeboah, D. A. (2006). The state of world fisheries from a fishworkers perspective: The Ghanaian situation. International Collective in Support of Fishworkers, India. 104 pp.
Google Scholar
16
-
Edwards, J., Gills A., & Abohweyere, P. (2001). A revision of Irvine’s marine fishes of tropical West Africa. Darwin Initiative Report, 2, 157.
Google Scholar
17
-
Le Cren, E. D. (1951). The length-weight relationship and seasonal cycle in gonadal weight.
Google Scholar
18
-
Lagler, K. F. (1956). Freshwater fisheries biology. William C. Brown. Co., Dubuque, Iowa, 421 p.
Google Scholar
19
-
Sparre, P., & Venema, S. C. (1992). Introduction to tropical fish assessment. Part I–Manual, FAO Fisheries Technical Paper, 306(1), 376.
Google Scholar
20
-
Pauly, D. & Munro, J. L. (1984). Once more on the comparison of growth in fish and invertebrates. ICLARM Fishbyte 2, 21 pp.
Google Scholar
21
-
King, M. (1995). Fisheries biology, assessment and management. Fishing News Books, Hartnolds Ltd, Bodmin, Cornwall, Great Britain. 341 pp.
Google Scholar
22
-
Pauly, D. (1980). On the interrelationships between natural mortality, growth parameters, and mean environmental temperature in 175 fish stocks. ICES Journal of Marine Science, 39(2), 175-192.
Google Scholar
23
-
Gulland, J. A. (1971). The fish resources of the ocean. West Byfleet, Surrey. Fishing News (Books), Ltd., for FAO, 255.
Google Scholar
24
-
Allam, S. M., Faltas, S. N., & Ragheb, E. (2004). Reproductive biology of Sphyraena species in the Egyptian Mediterranean waters off Alexandria. Egyptian Journal of Aquatic Research, 30, 255-270.
Google Scholar
25
-
Allam, S., Faltas, S., & Ragheb, E. (2005). Stock assessment of Barracuda, genus Sphyraena, along the Egyptian Mediterranean Coast. Egyptian Ministry of Commerce and Industry, 31(2), 281-292.
Google Scholar
26
-
Ayo-Olalusi, C. I., & Abeke-Ayoade, A. (2018). Population parameters of barracuda, Sphyraena afra (Family: Sphyraenidae) from coastal waters of Lagos State, Nigeria. Zoology and Ecology, 28(4), 376-383.
Google Scholar
27
-
Kasim, H. M. (2000). Fishery, stock assessment and management of the barracuda resource in India. In V. N. Pillai & N. G. Menon (Eds.), Central Marine Fisheries Research Institute (pp. 1-15) Kerala, India.
Google Scholar
28
-
Petrakis, G., & Stergiou, K. I. (1995). Weight-length relationships for 33 fish species in Greek waters. Fisheries Research, 21(3-4), 465-469.
Google Scholar
29
-
López, F., Jakes, U., Gonzalez, A., & Floresramírez, S. (2016). Length-weight and length-length relationships, and condition factor of the pelican barracuda Sphyraena idiastes (Perciformes: Sphyraenidae) in the Gulf of California, Mexico. California Fish and Game, 102(4), 183-187.
Google Scholar
30
-
Zavala-Leal, I., Palacios-Salgado, D., Ruiz-Velazco, J. M., Valdez-Gonzalez, F., Manuel Pacheco-Vega, J., Grana-dos-Amores, J., & Ramon Flores-Ortega, J. (2018). Reproductive aspects of Sphyraena ensis (Perciformes: Sphyraenidae) inhabiting the coast of San Blas Nayarit, southeast Gulf of California. California Fish and Game, 104(1), 7-18.
Google Scholar
31
-
Oliveira, M. T., Santos, M. N., Coelho, R., Monteiro, V., Martins, A., & Lino, P. G. (2015). Weight–length and length–length relationships for reef fish species from the Cape Verde Archipelago (tropical north‐eastern Atlantic). Journal of Applied Ichthyology, 31(1), 236-241.
Google Scholar
32
-
Gallardo-Cabello, M., Sarabia-Méndez, M., Espino-Barr, E., & Anislado-Tolentino, V. (2010). Biological aspects of Lutjanus peru in Bufadero Bay, Michoacán, México: growth, reproduction and condition factors. Revista de Biologia Marina y Oceanografia, 45(2).
Google Scholar
33
-
Razi, A., & Noori, A. (2018). Length-weight, condition factor and gonadosomatic index of blackspot snapper, Lutjanus fulviflamma (Forsskal, 1775) (Perciformes: Lutjanidae) in the northern Persian Gulf. International Journal of Aquatic Biology, 6(2), 66-74.
Google Scholar
34
-
De Sylva, D. P. (1963). Systematics and life-history of the great barracuda Sphyraena barracuda (Walbaum). Studies in Tropical Oceanography 1, 179. Retrieved from https://scholarlyrepository.miami.edu/trop_ocean/1.
Google Scholar
35
-
Allam, S. M., Faltas, S. N., & Ragheb, E. (2004). Age and growth of barracudas in the Egyptian Mediterranean waters. Egyptian Journal of Aquatic Research, 30(B), 281-289.
Google Scholar
36
-
Schmidt, T. W. (1989). Food habits, length-weight relationship and condition factor of young great barracuda, Syphraena barracuda (Walbaum), from Florida Bay, Everglades National Park, Florida. Bulletin of Marine Science, 44(1), 163-170.
Google Scholar
37
-
Rejitha, B. T., & Pillai, P. M. (2015). Estimation of length-weight relationship of six coral reef fishes of order Perciformes from Gulf of Mannar, southeast coast of India. International Journal of Fisheries and Aquatic Studies, 3(1): 305-307.
Google Scholar
38
-
Agboola, J. I. and Anetekhai, M. A. (2008). Length-weight relationships of some fresh and brackish water fishes in Badagry creek, Nigeria. Journal of Applied Ichthyology 24: 623-625.
Google Scholar
39
-
Newman, S. J., Williams, D. M., & Russ, G. R. (1996). Age validation, growth and mortality rates of the tropical snappers (Pisces: Lutjanidae) Lutjanus adetii (Castelnau, 1873) and L. quinquelineatus (Bloch, 1790) from the central Great Barrier Reef, Australia. Marine and Freshwater Research, 47(4), 575-584.
Google Scholar
40
-
Kumolu-Johnson, C. A., & Ndimele, P. E. (2010). Length-weight relationships and condition factors of twenty-one fish species in Ologe Lagoon, Lagos, Nigeria. Asian Journal of Agricultural Sciences, 2(4), 174-179.
Google Scholar
41
-
Gomez, G. J., Guzman, R. A., & Marcano, L. A. (1996). Biological aspects of the yellow eye snapper (Lutjanus vivanus) (Pisces: Lutjanidae) from the Los Hermanos Islands, Eastern Venezuela. Biology, fisheries, and culture of tropical groupers and snappers, 51-58.
Google Scholar
42
-
Bagenal, T. B. & Tesch, T. B. (1978). Age and growth In Bagenal, T. (Ed.), Methods for Assessment of Fish Production in Freshwaters, (3rd ed.). IBP Handbook No. 3, Oxford: Blackwell Science Publications. Pp. 101-136.
Google Scholar
43
-
Sumer, C., Ozdemir, G., & Ertekin, H. (2014). Age, growth and reproduction of the striped seabream, Lithognathus mormyrus (Pisces: Sparidae), in the Beymelek Lagoon (southwestern coast of Turkey). Cahiers de Biologie Marine, 55(1), 37-42.
Google Scholar
44
-
Lizama, M. D., & Ambrosio, A. M. (2002). Condition factor in nine species of fish of the Characidae family in the upper Paraná River floodplain, Brazil. Brazilian Journal of Biology, 62(1), 113-124.
Google Scholar
45
-
Kachari, A., Abujam, S., & Das, D. N. (2017). Length-weight relationship (LWR) and condition factor of Amblyceps apangi from Arunachal Pradesh, India. Journal of Aquaculture Engineering and Fisheries Research, 3, 97-107.
Google Scholar
46
-
Fagade, S. O. (1979). Observation of the biology of two species of Tilapia from the Lagos lagoon Nigeria. Bull. Inst. Fond Afr. Nore (Ser. A), 41, 627-658.
Google Scholar
47
-
Rao, M. R. (1985). Ecology and Biology of the Flat Fish Cynoglossus macrolepidotus (Bleeker, 1851) off Bombay Coast (Doctoral dissertation, University of Mumbai, Mumbai, India). Retrieved from http://aquaticcommons.org/15910/1/JIFA19_043.pdf.
Google Scholar
48
-
Blackwell, B.G., Brown, M. L. & Willis, D. W. (2000). Relative Weight (Wr) Status and Current Use in Fisheries Assessment and Management. Reviews in Fisheries Science, (8):1, 1-44, DOI: 10.1080/10641260091129161.
Google Scholar
49
-
Nikolsky, G. V. (1963). Ecology of fishes. In Ecology of fishes. Academic press, London and New York.352 pp.
Google Scholar
50
-
Hosseini, A., Kochanian, P., Marammazi, J., Yavari, V., Savari, A., & Salari-Aliabadi, M. A. (2009). Length-weight relationship and spawning season of Sphyraena jello from Persian Gulf. Pakistan Journal of Biological Sciences: PJBS, 12(3), 296-300.
Google Scholar
51
-
Cruz-Romero, M., Chávez, E. A., Espino, E., & García, A. (1996). Assessment of a snapper complex (Lutjanus spp.) of the eastern tropical Pacific. In Biology, fisheries and culture of tropical groupers and snappers. ICLARM Conference Proceedings 48, 324-330.
Google Scholar
52
-
Kasim, H.M., & Balasubramanian, T. S. (1990). Fishery, growth, yield per recruit and stock assessment of Sphyraena obtusata (Cuvier) off Tuticorin, Gulf of Mannar. Indian Journal of Fisheries, 37(4), 281-288.
Google Scholar
53
-
Abowei, J. F. N., & Davies, O. A. (2009). Aspects of Sphyraena barracuda (Wallbaum, 1992) population dynamics from the fresh water reaches of lower Nun River, Niger Delta, Nigeria. Current Research Journal of Biological Sciences, 1(1), 21-27.
Google Scholar
54
-
Stobberup K. A., Ramos V. D. M., Coelho M. L. (2004). Ecopath model of the Cape Verde coastal ecosystem. Fisheries Center Research Reports 12(7), 39–56.
Google Scholar
55
-
Amponsah S. K. K., Ofori-Danson P. K., Nunoo F. K. E. (2016). Study of the population parameters of the bigeye grunt, Brachydeuterus auritus (Valenciennes, 1831) in Ghanaian coastal waters and its implications for management. International Journal of Fisheries and Aquatic Studies, 4 (6): 413-419.
Google Scholar
56
-
Abowei, J. F. N., George, A. D. I., & Davies, O. A. (2010). Mortality, exploitation rate and Recruitment pattern of Callinectes amnicola (De Rochebrune) from Okpoka Creek, Nigeria Delta, Nigeria. Asian Journal of Agricultural Sciences, 2(1), 27-34.
Google Scholar
57
-
Martinez-Andrade, F. (2003). A comparison of life histories and ecological aspects among snappers (Pisces: Lutjanidae). (Doctoral Dissertations, Louisiana State University and Agricultural and Mechanical College, Louisiana, United States). Retrieved from https://digitalcommons.lsu.edu/gradschool_dissertations/2271.
Google Scholar
58
-
Haight, W. R., Kobayashi, D. R., & Kawamoto, K. E. (1993). Biology and management of deep-water snappers of the Hawaiian Archipelago. Marine Fisheries Review, 55(2), 20-27.
Google Scholar
59
-
Piddocke, T. P., Butler, G. L., Butcher, P. A., Stewart, J., Bucher, D. J., & Christidis, L. (2015). Age and growth of mangrove red snapper Lutjanus argentimaculatus at its cool‐water‐range limits. Journal of Fish Biology, 86(5), 1587-1600.
Google Scholar
60