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Describing the Body Shapes of three populations of Sardinella lemuru (Bleeker, 1853) from Mindanao Island, Philippines Using Relative Warp Analysis

Author Affiliations

  • 1Department of Biological Sciences, MSU-Iligan Institute of Technology, 9200 Iligan City, PHILIPPINES

Int. Res. J. Biological Sci., Volume 3, Issue (6), Pages 6-17, June,10 (2014)

Abstract

This study utilized landmark-based geometric morphometrics to determine and describe the body shape variation of Sardinella lemuru populations collected from the bays of Butuan City, Dipolog City, and Pagadian City in Mindanao, Philippines. A total of 30 males and 30 females from each sampling site were digitized and landmarked using 18 landmark points in the fish’s body. Relative warps (RW) for within and between populations were obtained. Significant results for variation between sexes were emphasized by multivariate analysis of variance (MANOVA), canonical variate analysis (CVA), and discriminant function analysis (DFA). RWs show that females exhibit body shapes that are geared to support large number of eggs (i.e. distended belly area) ensuring successful reproductive rate while males exhibit a more slender body and are generally smaller than females. Significant differences were also observed between populations of S. lemuru which can be attributed to geographic isolation permitting little to no interaction between populations. Environmental factors, overfishing/overexploitation could also be considered as factors influencing these morphological variations. Hence, this study showed that landmark-based geometric morphometric methods is an effective tool in describing body shape variations that exist within and between populations of S. lemuru. This initial method in distinguishing between populations is important in proper management of these species.

References

  1. Pileggi J. and Thomson B., Fisheries of the United States, 1978, US-NMFS, 7800:120 (1979)
  2. Samonte I.E., Pagulayan R.C., Mayer W.E., Molecular Phylogeny of Philippine Freshwater Sardines Based on Mitochondrial DNA Analysis, The American Genetic Association, 91, 247-253 (2000)
  3. Willette D.A., Bognot E.D.C., Mutia T.M., Santos M.D., Biology and Ecology of Sardines in the Philippines: A Review. Final Draft (2011)
  4. BFAR (Bureau of Fisheries and Aquatic Resources), Philippine fisheries profile Department of Agriculture-BFAR, Manila, Philippines. 54 p. (2000)
  5. Thomas R., Willette D., Santos M., Phylogeography of the goldstripe Sardinella, Sardinella gibbosa, and the Bali Sardinella, Sardinella lemuru, in the Philippine archipelago. Open Conference Systems, 11th National Symposium in Marine Science (2011)
  6. Sustainable Fisheries Partnership, FishSource Profile for Bali sardinella - stock units undefined [FIP: Bali sardinella, SFP]. World Wide Web Electronic Publication Available at http://www.fishsource.com/site/goto_profile_by_uuid/059e7bc0-bfb2-11de-b141-daf105bfb8c2 accessed 2013-08-07 last updated May 4, (2013)
  7. Guanco M.R., Mesa S.V., Belga P.B, Nunal D.R.M., Assessment of the commercial fisheries of Western and Central Visayan Sea, BFAR NFRDI Technical Paper Series 12(1), 1-44 (2009)
  8. Fisheries-induced Evolution. World Wide Web Electronic Article Available at http://webarchive.iiasa.ac.at/Research /EEP/FinE/Objectives.html (2013)
  9. Dorado E., Torres M.A., Demayo C.G., Describing Body Shapes of the White Goby, Glossogobius giuris of Lake Buluan in Mindanao, Philippines using landmark-based geometric morphometric analysis, International Research Journal of Biological Sciences, 1(7), 33-37 (2012)
  10. Nacua S.S., Torres M.A., Demayo, C.G., Sexual Dimorphism in Body Shape of Hypseleotris agilis (Herre, 1927) from Lake Lanao, Philippines, International Research Journal of Biological Sciences, 1(2), 25-31 (2012)
  11. Torres M.A.J., Joshi R.C., Sebastian L.S., Demayo C.G., Geographic phenetic variation in the goldenapple snail, Pomacea canaliculata (Ampullariidae) based on geometric approaches to morphometrics, AESBioflux,3(3), 243-258 (2011)
  12. Webb P.W., Body form, locomotion and foraging in aquatic vertebrates, Amer. Zool.,24, 107–120 (1984)
  13. Walker J.A., Ecological morphology of lacustrine threespine stickleback Gasterosteus aculeatus L. (Gasterosteidae) body shape, Biological Journal of the Linnean Society,61, 3-50 (1997)
  14. Pakkasmaa S. and Piironen J., Morphological differentiation among local trout (Salmo trutta) populations, Biological Journal of the Linnean Society, 72, 231–239 (2001)
  15. Schluter D., Adaptive radiation in sticklebacks: size, shape, and habitat use efficiency, Ecology, 74, 699–709 (1993)
  16. Klingenberg C.P. and Ekau W.A., combined morphometric and phylogenetic analysis of an ecomorphological trend: pelagization in Antarctic fishes (Perciformes: Nototheniidae), Biological Journal of the Linnean Society, 59, 143–177 (1996)
  17. Caldecutt W.J. and Adams D.C., Morphometrics of trophic osteology in the threespine stickleback, Gasterosteus aculeatus, Copeia, 1998: 827–838 (1998)
  18. Douglas M.E., Douglas M.R., Lynch J.M., McElroy D.M., Use of geometric morphometrics to differentiate Gila(Cyprinidae) within the upper Colorado River Basin, Copeia, 2001: 389-400 (2001)
  19. R¨uber L., and Adams D.C., Evolutionary convergence of body shape and trophic morphology in cichlids from Lake Tanganyika, J. Evol. Biol.,14, 325–332 (2001)
  20. Hulsey C.D. and Wainwright P.C., Projecting mechanics into morphospace: disparity in the feeding system of labrid fishes, Proceedings of the Royal Society of London B, Biological Sciences,269, 317–326 (2002)
  21. Rohlf F.J., and Marcus L.F., A revolution in morphometrics, Trends in Ecology & Evolution, 8(4), 129–132 (1993)
  22. Rohlf F.J., NTSYSpc: Numerical Taxonomy System, ver. 2.20, Exeter Publishing, Setauket, NY. (2008)
  23. Darwin C., The Descent of Man and Selection in Relation to Sex. Humbolt, New York (1874)
  24. Anderson, M., Sexual Selection. Princeton University Press, Princeton, New Jersey (1994)
  25. Corti M., Loy A., Cataudella S., Form changes in the sea bass, Dicentrarchus labrax (Moronidae: Teleostei), after acclimation to freshwater: an analysis using shape coordinates, Environ. Biol. Fish., 47, 165–175 (1996)
  26. Dorado E., Torres M.A., Demayo C.G., Sexual Dimorphism in body shapes of the spotted barb fish, Puntius binotatus of Lake Buluan in Mindanao, Philippines, AACL Bioflux,5(5), 321-329 (2012)
  27. Slatkin M., Ecological causes of sexual dimorphism, Evolution, 38, 622–630 (1984)
  28. Shine R., Ecological causes for the evolution of sexual dimorphism: a review of the evidence, The Quarterly Review of Biology, 64, 419–461 (1989)
  29. Parker G.A., The evolution of sexual size dimorphism in fish, Journal of Fish Biology41, 1–20 (1992)
  30. Kitano J., Mori S., Peichel C.L. Sexual Dimorphism in the External Morphology of the Threespine Stickleback Gasterosteus aculeatus), Copeia,, 336-349 (2007)
  31. Mori S., The breeding system of the threespined stickleback, Gasterosteus aculeatus (forma leiura) with reference to spatial and temporal patterns of nesting activity, Behaviour. 126, 97–124 (1993)
  32. Candolin U., and Voigt H.R., Size-dependent selection on arrival times in sticklebacks: why small males arrive first, Evolution, 57, 862–871 (2003)
  33. Wiley T., Simpfendorfer C., Faria V., Mcdavitt M., Range, sexual dimorphism and bilateral asymmetry of rostral tooth counts in the small tooth sawfish Pristis pectinata Latham (Chondrichthyes: Pristidae) of the southeastern United States, Zootaxa, 1810, 51- 59 (2008)
  34. Spoljaric M.A. and Reimchen T.E., Habitat-dependent reduction of sexual dimorphism in geometric body shape of Haida gwaii threespine stickleback, Biological Journal of the Linnean Society, 95, 505–516 (2008)
  35. Turan C., Erguden D., Turan F., Gurlek M., Genetic and Morphologic Structure of Liza abu (Heckel, 1843) Populations from the Rivers Orontes, Euphrates and Tigris, Turk J Vet. Anim. Sci.,28, 729-734 (2004)
  36. Turan C., Erguden D., Gurlek M., Basusta N., Turan F., Morphometric Structuring of the Anchovy (Engraulis encrasicolus L.) in the Black, Aegean and Northeastern Mediterranean Seas, Turk J Vet. Anim. Sci,28, 865-871 (2004)
  37. Stearns S.C., A Natural Experiment in Life-history Evolution: Field data on the introduction of Mosquitofish Gambusia affinis) to Hawaii, Evolution, 37, 601-617 (1983)
  38. Rijnsdorp A. D., Fisheries as a large-scale experiment on life-history evolution: disentangling phenotypic and genetic effects in changes in maturation and reproduction of North Sea plaice, Pleuronectes platessa L., Oecologia, 96, 391–401 (1993)
  39. Stokes K. and Law R., Fishing as an evolutionary force, Mar. Ecol. Prog. Ser.,208, 307–309 (2000)
  40. Allendorf F.W., Ryman N., Utter F., Genetics and fishery management: Past, present and future in populations genetics and fisheries management (N. Ryman and F. Utter, Eds.) University of Washington Press, Seattle and London. pp1-20 (1987)
  41. Wimberger P.H., Plasticity of fish body shape - the effects of diet, development, family and age in two species of Geophagus (Pisces: Chichlidae), Biol. J. Linn. Soc.,45, 197-218 (1992)