Acta Nat. Sci.   |  e-ISSN: 2718-0638

Original article | Acta Natura et Scientia 2021, Vol. 2(2) 118-123

Determination of Sexual Dimorphism in the Freshwater Blenny, Salaria fluviatilis (Asso, 1801), Distributed in Brackish Water Habitats

Sule Gurkan & Deniz Innal

pp. 118 - 123   |  DOI: https://doi.org/10.29329/actanatsci.2021.350.05   |  Manu. Number: MANU-2109-29-0003.R1

Published online: November 01, 2021  |   Number of Views: 73  |  Number of Download: 697


Abstract

The present study aimed to determine the presence of the sexual dimorphism based on the morphometric measurements in a total of 60 samples (♀: 26; ♂: 14, immature; 20) which were obtained in April 2017 from the population of Salaria fluviatilis which shows distribution in the brackish waters in the Karpuzçay Creek (Antalya, Turkey). As a result of the morphometric analysis performed in both sexes of samples, it has been determined that there were differences between body parts in terms of total length (TL), dorsal fin length (DFL), snout length, and eye diameters in the head area. Accordingly, it has been observed that the lengths of allometric growing body parts of males were greater than that of females. The properties of sexual dimorphism in the body parts of freshwater blenny cause significant differences between sexes in brackish water forms. The differences in male individuals such as TL and long DFL are important criteria for the selection of large male individuals for sexual selection in mating. It was thought that the increase in snout length and eye diameter in the head region gives males some advantages in various areas such as feeding performance from the habitat, male selection of females in mating, and swimming performance.

Keywords: Blennid species, Salaria fluviatilis, Dimorphic structure, Morphometric features, Phenotypic response


How to Cite this Article?

APA 6th edition
Gurkan, S. & Innal, D. (2021). Determination of Sexual Dimorphism in the Freshwater Blenny, Salaria fluviatilis (Asso, 1801), Distributed in Brackish Water Habitats . Acta Natura et Scientia, 2(2), 118-123. doi: 10.29329/actanatsci.2021.350.05

Harvard
Gurkan, S. and Innal, D. (2021). Determination of Sexual Dimorphism in the Freshwater Blenny, Salaria fluviatilis (Asso, 1801), Distributed in Brackish Water Habitats . Acta Natura et Scientia, 2(2), pp. 118-123.

Chicago 16th edition
Gurkan, Sule and Deniz Innal (2021). "Determination of Sexual Dimorphism in the Freshwater Blenny, Salaria fluviatilis (Asso, 1801), Distributed in Brackish Water Habitats ". Acta Natura et Scientia 2 (2):118-123. doi:10.29329/actanatsci.2021.350.05.

References
  1. Akşiray, F. (1987). Türkiye deniz balıkları tayın anahtarı. İstanbul Üniversitesi Fen Fakültesi Hidrobiologi Araştırma Enstitüsü Yayınları (in Turkish). [Google Scholar]
  2. Alp, A., & Kara, C. (2007). Distribution pattern and morphological differences between the sexes of river blenny, Salaria fluviatilis (Asso, 1801), in the Ceyhan River Basin, Turkey. Turkish Journal of Zoology, 31(2), 113-120. [Google Scholar]
  3. Bergmann, C. (1847). Ueber die Verhältnisse der Wärmeökonomie der Thiere zu ihrer Grösse. Gottinger Studien, vol. 3, pp. 595-708. [Google Scholar]
  4. Choo, C. K., & Liew, H. C. (2006). Morphological development and allometric growth patterns in the juvenile seahorse Hippocampus kuda Bleeker. Journal of Fish Biology, 69(2), 426-445. https://doi.org/10.1111/j.1095-8649.2006.01105.x [Google Scholar] [Crossref] 
  5. Côte, I. M., & Hunte, W. (1989). Male and female mate choice in the redlip blenny: why bigger is better. Animal Behaviour, 38(1), 78-88. https://doi.org/10.1016/S0003-3472(89)80067-3 [Google Scholar] [Crossref] 
  6. Côté, I. M., Vinyoles, D., Reynolds, J. D., Doadrioc, I.,& Perdices, A. (1999). Potential impacts of gravel extraction on Spanish populations of river blennies Salaria fuviatilis (Pisces, Blenniidae). Biological Conservation, 87(3), 359-367. https://doi.org/10.1016/S0006-3207(98)00072-X [Google Scholar] [Crossref] 
  7. Crivelli, A. J. (1996). The freshwater fish endemic to the Mediterranean region. An action plan for their conservation. Tour du Valat Publication (in French). [Google Scholar]
  8. Crivelli, A. J. (2006). Salaria fluviatilis. The IUCN Red List of Threatened Species 2006: e.T60764A12407160. https://dx.doi.org/10.2305/IUCN.UK.2006.RLTS.T60764A12407160.en. Downloaded on 31 October 2021. [Google Scholar]
  9. Fabre, N., Oliva, F., Garcia-Galea, E., & Vinyoles, D. (2014). Plasticity in secondary sexual characteristics in male freshwater blenny Salaria fluviatilis. Canadian Journal of Zoology, 92(6), 537-543. https://doi.org/10.1139/cjz-2013-0233 [Google Scholar] [Crossref] 
  10. Gulland, J. A. (1969). Manual of methods for fish stock assessment. Part 1. Fish population analysis. FAO, Rome, Italy. [Google Scholar]
  11. Innal, D. (2019). Diversity and length-weight relationships of Blennid Species Actinopterygii, Blenniidae) from Mediterranean Brackish Waters in Turkey. Aquatic Sciences and Engineering, 34(3), 96-102. https://doi.org/10.26650/ASE2019573052 [Google Scholar] [Crossref] 
  12. Keith, P., Persat, H., Feunteun, E., & Allardi, J. (2011). Les Poissons d’eau douce de France. Muséum national d'Histoire naturelle, Paris; Biotope, Mèze, 552 p. (Inventaires & biodiversité ; 1). [Google Scholar]
  13. Kottelat, M., & Freyhof, J. (2007). Handbook of European freshwater fishes. Publications Kottelat. [Google Scholar]
  14. Laporte, M., Berrebi, P., Claude, J., Vinyoles, D., Pourovira, Q., Raymond, J-D. & Magnan, P. (2018). The ecology of sexual dimorphism in size and shape of the freshwater blenny Salaria fluviatilis. Current Zoology, 64(2), 183-191. https://doi.org/10.1093/cz/zox043 [Google Scholar] [Crossref] 
  15. Laporte, M., Claude, J., Berrebi, P., Perret, P., & Magnan, P. (2016a). Shape plasticity in response to water velocity in the freshwater blenny Salaria fluviatilis. Journal of Fish Biology, 88(3), 1191-1203. https://doi.org/10.1111/jfb.12902 [Google Scholar] [Crossref] 
  16. Laporte, M., Dalziel, A. C., Martin, N., & Bernatchez, L. (2016b). Adaptation and acclimation of traits associated with swimming activity in Lake Whitefish (coregonus clupeaformis) ecotypes. BMC Evolutionary Biology, 16, 160. https://doi.org/10.1186/s12862-016-0732-y [Google Scholar] [Crossref] 
  17. Laporte, M., Mattei, J., Perret, P., Roché, B., Vinyoles, D., Goren M., Bacha M., Mourad Z., Pou i Rovira Q., Berrebi P., & Magnan P. (2013). New maximum lengths for freshwater blenny (Salaria fluviatilis Asso, 1801) and length comparison between continental and island rivers. Cybium, 37(4), 309-313. https://doi.org/10.26028/cybium/2013-374-013 [Google Scholar] [Crossref] 
  18. Neat, F. C., Lengkeek, E. P., Westerbeek, E. P., Laarhoven, B., & Videller, J. J. (2003). Behavioural and morphological differences between lake and river populations of Salaria fluviatilis. Journal of Fish Biology, 63(2), 374-387. https://doi.org/10.1046/j.1095-8649.2003.00159.x [Google Scholar] [Crossref] 
  19. Rensch, B. (1950). Die Abhängigkeit der relativen Sexualdifferenz von der Körpergröße. Bonner zoologische Beiträge, 1, 58-69 (in German). [Google Scholar]
  20. Rispoli, V. F., & Wilson, A. B. (2008). Sexual size dimorphism predicts the frequency of multiple mating in the sex-role reversed pipefish Syngnathus typhle. Journal of Evolutionary Biology, 21(1), 30-38. https://doi.org/10.1111/j.1420-9101.2007.01470.x [Google Scholar] [Crossref] 
  21. Roché, B. (2001). Atlas des poissons d’eau douce de Corse. Direction régionale de l’environnement Corse. Imprimerie Bastiaise, Bastia, Corse. [Google Scholar]
  22. Shine, R. (1989). Ecological causes for the evolution of sexual dimorphism: a review of the evidence. Quarterly Review of Biology, 64(4), 419-461. https://doi.org/10.1086/416458 [Google Scholar] [Crossref] 
  23. Vinyoles, D., & De Sostoa, A. (2007). Life-history traits of the endangered river blenny Salaria fluviatilis (Asso, 1801) and their implications for conservation. Journal of Fish Biology, 70(4), 1088-1108. https://doi.org/10.1111/j.1095-8649.2007.01371.x [Google Scholar] [Crossref]