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Asian Journal of Animal and Veterinary Advances

Year: 2012 | Volume: 7 | Issue: 10 | Page No.: 921-927
DOI: 10.3923/ajava.2012.921.927
Meristic, Morphometrics and Length-weight Relationship of Tropical Silverside, Atherinomorus duodecimalis (Valenciennes in Cuvier and Valenciennes, 1835) in Seagrass and Mangrove Habitats of Tinggi Island, Johor, Malaysia
A.G. Mazlan, Y.S. Chung, C.C. Zaidi, A. Samat, A. Arshad, Y.G. Seah, Gazi Mahabubul Alam and K.D. Simon

Abstract: The present study describes the meristic, morphometric and Length Weight Relationship (LWR) of tropical silverside, Atherinomorus duodecimalis (Atheriniformes: Atherinidae) an important fishery in the Sea grass and mangrove habitat of Tinggi Island, Johor, Malaysia. A series of sampling survey was conducted in seagrass and mangrove habitats of Tinggi Island, using beach seine net. A total of 94 specimens (3.7-10.3 cm TL) used in this study. The results showed that meristic and morphometric features of the fish studied agreed well with a description of the holotype specimen MNHN A. 4382 and other silverside specimens. The only exception was observed in the upper jaw length and eye diameter as a percentage of head length. The allometric coefficient ‘b’ of the length weight relationship indicated negative allometric growth (b<3.0) in seagrass habitat and positive allometric growth (b>3.0) in mangrove habitat. To the best knowledge of the authors, this study presented the first reference on LWR for this species from Johor waters, Malaysia.

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A.G. Mazlan, Y.S. Chung, C.C. Zaidi, A. Samat, A. Arshad, Y.G. Seah, Gazi Mahabubul Alam and K.D. Simon, 2012. Meristic, Morphometrics and Length-weight Relationship of Tropical Silverside, Atherinomorus duodecimalis (Valenciennes in Cuvier and Valenciennes, 1835) in Seagrass and Mangrove Habitats of Tinggi Island, Johor, Malaysia. Asian Journal of Animal and Veterinary Advances, 7: 921-927.

Keywords: mangrove, Population growth, habitat, Atherinomorus duodecimalis and coastal waters

INTRODUCTION

The atherinid tropical silverside A. duodecimalis (family Atherinidae) is stenohaline fish and widely distributed in the eastern Indian and West Pacific Oceans (Ivantsoff and Crowley, 1991; Takemura et al., 2004). This fish species is commonly available in shallow coastal waters, estuaries, mangrove habitats and seagrass habitats (Matsuura and Kimura, 2005). It usually occurs in schools along shorelines and underneath the jetty facilities of the populated islands. Planktonic eggs of this species are easily recognized by observing the entangling filaments on chorion membrane.

Fig. 1: Atherinomorus duodecimalis (Carpenter and Niem, 1999)

This fish is important as forage for commercial fishes and used as bait and dried cat food (Ivantsoff and Crowley, 2000). Detail studies on the meristic, morphometric characteristic and length-weight relationship of A. duodecimalis (Fig. 1) are still lacking in Malaysia coastal waters.

Comparing anatomical features of organisms has been the basis for taxonomic classification of organisms and differentiation among stocks as well as closely related species. Those comparisons are usually carried out using differences in body measurements (morphometry) or differences in numbers of anatomical structures (meristics) (Bagenal, 1978; Bookstein, 1991).

LWRs are useful in fishery management for both applied and basic use (Pitcher and Hart, 1982) to: (i) estimate weight from length observations, (ii) calculate production and biomass of a fish population and/or (iii) provide information on stocks or organism condition at the corporal level.

Therefore, in the present study, we examined the meristic, morphometric characteristic and LWR of A. duodecimalis available in the seagrass and mangrove habitats of Tinggi Island, Johor, Malaysia.

MATERIALS AND METHODS

A series of catch survey was carried out in the seagrass and mangrove habitats of Tinggi Island, Johor using beach seine net (100 ftx6 ft; 5 mm mesh size) from January 2008 to December 2009. All catches were sorted in accordance to the standard protocol listed by Sparre and Venema (1998). Fresh sub-samples were kept in the ice chest prior to further biological investigation at Tinggi Island field-laboratory. Species identification was made in accordance to Masuda et al. (1984), Ivantsoff and Crowley (2000), Matsuura et al. (2000), Kimura et al. (2001) and Kimura and Matsuura (2003). Counts and measurements generally followed Hubbs and Lagler (1958) and Simon et al. (2010a). All measurements were made with a digital caliper (absolute digimatic digital calipers, Mitutoyo, Japan) to the nearest 0.01 cm and weighed to the nearest 0.1 g. All sub-samples were then fixed in 10% formalin prior to the laboratory analyses and further preserved in the 70% alcohol. Length-weight Relationships (LWRs) were calculated using the allometric regression analysis (W = aLb) (Le Cren, 1951; Abdallah, 2002; Ekelemu and Samuel, 2006; Bayhan et al., 2008; Simon et al., 2009; Ozvarol et al., 2010; Sivashanthini et al., 2009; Bok et al., 2011; Sasi and Berber, 2012).

RESULTS AND DISCUSSION

In this study, a total number of 94 A. duodecimalis individual was collected from seagrass (n = 47) and mangrove habitats (n = 47). Meristic counts and measurements of this individual are shown in Table 1.

Table 1: Counts and measurements of the holotype, other specimens and Tinggi Island specimens of Atherinomorus duodecimalis
Figures in parentheses indicate mean values, holotype and other specimen’s measurements were taken from Kimura et al. (2001)

Measurements of morphometric characteristic were given in mean values and expressed in relative percentage to standard length, head length, pelvic fin length and caudal peduncle depth. Relationship between morphometric parameters with standard length of A. duodecimalis from seagrass and mangrove habitats are shown in Fig. 2. Two different habitats displayed different size fishes have been caught in this study but established totally similar pattern of morphometric characteristic in relationship with standard length.

In general, the meristic and morphometric positions of the fishes studied agreed well with the holotype specimen MNHN A. 4382 and other silverside specimens documented by Kimura et al. (2001). The only exceptions were slight differences in the upper jaw length and eye diameter (expressed as a percentage of head length). Variations occur in meristic and morphometric characteristic among similar species of fish from different geographic location were reported to be influenced by the environmental variables (Jennings et al., 2001; King, 1995; Bagenal, 1978). Detail population growth condition of this species was estimated using the allometric regression analysis (W = aLb).

Fig. 2(a-b): Relationship between morphometric parameters with standard length of from (a) Seagrass habitat and (b) Mangrove habitat

Fig. 3(a-b): Length-weight relationship of Atherinomorus duodecimalis from (a) Seagrass habitat and (b) Mangrove habitat

The results showed that the regression coefficient ‘b’ of A. duodecimalis was 2.75±0.13 (χ2 = 0.352; r2 = 0.953) for seagrass habitat and 3.81±0.33 (χ2 = 0.033; r2 = 0.695) for mangrove habitat (Fig. 3). The specimens collected from the seagrass habitat were found larger in size compared with collected from mangrove habitat. However, the population growth pattern as elucidated from a regression coefficient ‘b’ values demonstrated different pattern of a population growth conditions between these two habitats. The results indicated that atherinids collected from seagrass habitat displayed a negative allometric population growth pattern (b<3.0), in comparison with the fish collected in the mangrove habitat displayed a positive allometric population growth pattern (b>3.0).

The results also denoted that fishes collected from mangrove habitat have a weight increase faster than length, showing that this habitat provides abundant food supply in comparison to seagrass habitat. The functional roles of mangrove’s environment as major feeding and nursery ground for wide ranges of euryhaline fish species are documented (Faunce et al., 2004; Robertson and Duke, 1987). However, the ‘b’ values also changes due to changes in physiological growth condition such as food availability and gonads development for the respective population (Le Cren, 1951; Jennings et al., 2001; Simon et al., 2010b).

CONCLUSIONS

This study has described the meristic, morphometric and length-weight relationship of A. duodecimalis in Malaysian coastal waters. The results showed that meristic and morphometric features of the fish studied agreed well with the description of the holotype specimen MNHN A. 4382 and other silverside specimens. However, this study also reported the distinction in the upper jaw length and eye diameter as a percentage of head length from the holotype MNHN A. 4382 and other silverside specimens. The LWR obtained from the present study showed negative allometric growth (b<3.0) in seagrass samples while positive allometric growth (b>3.0) in mangrove samples. To the best of our knowledge, this study presented the first reference on the LWR for this fish species from Johor waters, Malaysia. Recent development in taxonomic revisions among the atherinids fish has revealed a need to re-describe a group of morphologically similar silverside in the Malaysian coastal waters.

ACKNOWLEDGMENTS

We would like to express our sincere gratitude to Professor Seishi Kimura for his constructive advice in writing this manuscript. We also would like to thanks anonymous referees for their useful comments. This work was supported by Ministry of Science, Technology and Innovation, Malaysia through Science Fund No. 04-01-02-SF0180 and Universiti Kebangsaan Malaysia through Young Researcher Incentive Grant No. GGPM-2011-057.

REFERENCES

  • Abdallah, M., 2002. Length-weight relationship of fishes caught by Trawl off Alexandria, Egypt. Naga ICLARM Quart., 25: 19-20.
    Direct Link    


  • Bagenal, T.B., 1978. Methods for Assessment of Fish Production in Freshwaters. 3rd Edn., Blackwell Scientific Publication, Oxford, UK., Pages: 365


  • Bayhan, B., T.M. Sever and E. Taskavak, 2008. Age, length-weight relationships and diet composition of scaldfish Arnoglossus laterna (Walbaum, 1792) (Pisces: Bothidae) in Izmir Bay (Aegean Sea). J. Anim. Vet. Adv., 7: 924-929.
    Direct Link    


  • Bok, T.D., D. Gokturk, A.E. Kahraman, T.Z. Alicli, T. Acun and C. Ates, 2011. Length-weight relationships of 34 fish species from the Sea of Marmara, Turkey. J. Anim. Vet. Adv., 10: 3037-3042.
    Direct Link    


  • Bookstein, F.L., 1991. Morphometric Tools for Landmark Data: Geometry and Biology. Cambridge University Press, Cambridge, London
    CrossRef    


  • Carpenter, K.E. and V.H. Niem, 1999. The Living Marine Resources of the Western Central Pacific. Volume 4. Bony Fishes part 2 (Mugilidae to Carangidae). FAO, Rome, pp: 2069-2790


  • Faunce, C.H., J.E. Serafy and J.J. Lorenz, 2004. Density-habitat relationships of mangrove creek fishes within the southeastern saline Everglades (USA), with reference to managed freshwater releases. Wetland Ecol. Manage., 12: 377-394.
    CrossRef    


  • Ekelemu, K.J. and A.A.Z. Samuel, 2006. Growth patterns and condition factors of four dominant fish species in Lake Ona, Southern Nigeria. J. Fish. Int., 1: 157-162.
    Direct Link    


  • Hubbs, C.L. and K.F. Lagler, 1958. Fishes of the Great Lakes Region. 2nd Edn., University of Michigan Press, Ann Arbor, MI., USA., pp: 213


  • Ivantsoff, W. and L.E.L.M. Crowley, 1991. Review of the Australian silverside fishes of the genus Atherinomorus (Atherinidae). Aust. J. Mar. Freshwat. Res., 42: 479-505.
    Direct Link    


  • Ivantsoff, W. and L.E.L.M. Crowley, 2000. Family Atherinidae, Silversides or Hardyheads. In: FAO Species Identification Guide for Fishery Purposes: The Living Marine Resources of the Western Central Pacific, Carpenter, K.E. and V.H. Niem (Eds.). Vol. 4, Food and Agriculture Organization of the United Nations, Rome, Italy, pp: 2113-2139


  • Jennings, S., M.J. Kaiser and J.D. Reynolds, 2001. Marine Fisheries Ecology. Blackwell Science Publishing, Oxford, UK., ISBN-13: 9780632050987, Pages: 417


  • Kimura, S., Y. Iwatsuki and T. Yoshino, 2001. Redescriptions of the Indo-West Pacific atherinid fishes, Atherinomorus endrachtensis (Quoy and Gaimard, 1825) and A. duodecimalis (Valenciennes in Cuvier and Valenciennes, 1835). Ichthyol. Res., 48: 167-177.
    CrossRef    


  • Kimura, S. and K. Matsuura, 2003. Fishes of Bitung, Northern Tip of Sulawesi, Indonesia. Ocean Research Institute, University of Tokyo, Tokyo, Japan, Pages: 244


  • King, M., 1995. Fisheries Biology: Assessment and Management. Fishing News Books Publ., Oxford, UK., ISBN-13: 978-0852382233, Pages: 341


  • Le Cren, E.D., 1951. The length-weight relationship and seasonal cycle in gonad weight and condition in the perch (Perca fluviatilis). J. Anim. Ecol., 20: 201-219.
    CrossRef    Direct Link    


  • Masuda, H., K. Amaoka, C. Araga, T. Uyeno and T. Yoshino, 1984. The Fishes of the Japanese Archipelago. Tokai University Press, Tokyo, Japan, Pages: 437


  • Matsuura, K. and S. Kimura, 2005. Fishes of Libong Island: West Coast of Southern Thailand. Ocean Research Institute, Tokyo, Japan, Pages: 78


  • Matsuura, K., O.K. Sumadhiharga and K. Tsukamoto, 2000. Field Guide to Lombok Island: Identification Guide to Marine Organisms in Seagrass Beds of Lombok Island, Indonesia. University of Tokyo, Tokyo, Japan Pages: 449


  • Ozvarol, Z.A.B., B.A. Balci, M.G.A. Tasli, Y. Kaya and M. Pehlivan, 2010. Age, growth and reproduction of goldband goatfish (Upeneus moluccensis Bleeker (1855)) from the Gulf of Antalya (Turkey). J. Anim. Vet. Adv., 9: 939-945.
    Direct Link    


  • Robertson, A.I. and N.C. Duke, 1987. Mangroves as nursery sites: Comparisons of the abundance and species composition of fish and crustaceans in mangroves and other nearshore habitats in tropical Australia. Mar. Biol., 96: 193-205.
    CrossRef    Direct Link    


  • Sasi, H. and S. Berber, 2012. Age, growth and some biological characteristics of white bream (Blicca bjoerkna L., 1758) in Uluabat lake, in Northwestern of Anatolia. Asian J. Anim. Vet. Adv., 7: 262-267.
    CrossRef    Direct Link    


  • Simon, K.D., Y. Bakar, A. Samat, C.C. Zaidi, A. Aziz and A.G. Mazlan, 2009. Population growth, trophic level, and reproductive biology of two congeneric archer fishes (Toxotes chatareus, Hamilton 1822 and Toxotes jaculatrix, Pallas 1767) inhabiting Malaysian coastal waters. J. Zhejiang Univ. Sci. B, 10: 902-911.
    CrossRef    


  • Simon, K.D., A.G. Mazlan, A. Samat, C.C. Zaidi and A. Aziz, 2010. Size, growth and age of two congeneric archer fishes (Toxotes jaculatrix Pallas, 1767 and Toxotes chatareus Hamilton, 1822) inhabiting Malaysian coastal waters. Sains Malaysiana, 39: 697-704.
    Direct Link    


  • Simon, K.D., Y. Bakar, S.E. Temple and A.G. Mazlan, 2010. Morphometric and meristic variation in two congeneric archer fish species (Toxotes chatareus, Hamilton 1822 and Toxotes jaculatrix, Pallas 1767) inhabiting Malaysian coastal waters. J. Zhejiang. Univ. Sci. B, 11: 871-879.
    PubMed    


  • Takemura, I., T. Sado, Y. Maekawa and S. Kimura, 2004. Descriptive morphology of reared eggs, larvae and juveniles of marine atherinids fish Atherinomorus duodecimalis. Ichthyol. Res., 51: 159-164.
    CrossRef    Direct Link    


  • Sparre, P. and S.C. Venema, 1998. Introduction to tropical fish stock assessment. Manual FAO Fisheries Technical Paper 306/1, Rev. 2, Rome, pp: 407.


  • Sivashanthini, K., G.A. Charles and W.S. Thulasitha, 2009. Length-weight relationship and growth pattern of Sepioteuthis lessoniana lesson 1830 (Cephalopoda: Teuthida) from the Jaffna Lagoon, Sri Lanka. J. Biol. Sci., 9: 357-361.
    CrossRef    Direct Link    


  • Pitcher, T.J. and P.J.B. Hart, 1982. Fisheries Ecology. Croom Helm, North, Central and South America, ISBN-13: 9780870554056, Pages: 414

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