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Hormone and Metabolite Profiles in Nesting Green and Flatback Turtles: Turtle Species with Different Life Histories

DOI: 10.1155/2014/503209

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Abstract:

Herbivorous turtle, Chelonia mydas, inhabiting the south China Sea and breeding in Peninsular Malaysia, and Natator depressus, a carnivorous turtle inhabiting the Great Barrier Reef and breeding at Curtis Island in Queensland, Australia, differ both in diet and life history. Analysis of plasma metabolites levels and six sex steroid hormones during the peak of their nesting season in both species showed hormonal and metabolite variations. When compared with results from other studies progesterone levels were the highest whereas dihydrotestosterone was the plasma steroid hormone present at the lowest concentration in both C. mydas and N. depressus plasma. Interestingly, oestrone was observed at relatively high concentrations in comparison to oestradiol levels recorded in previous studies suggesting that it plays a significant role in nesting turtles. Also, hormonal correlations between the studied species indicate unique physiological interactions during nesting. Pearson correlation analysis showed that in N. depressus the time of oviposition was associated with elevations in both plasma corticosterone and oestrone levels. Therefore, we conclude that corticosterone and oestrone may influence nesting behaviour and physiology in N. depressus. To summarise, these two nesting turtle species can be distinguished based on the hormonal profile of oestrone, progesterone, and testosterone using discriminant analysis. 1. Introduction Hormones have various functions across animal taxa. In birds, for example, testosterone is linked to mating success, while corticosterone has been shown to support energetically demanding processes [1]. In vertebrates glucocorticoid hormones can assist in the modulation of life-history events, survival probabilities, and fecundity [2]. Similarly steroid hormones play an essential role in the reproductive behaviour and sexual development in marine turtles [3]. Sex determination in sea turtles is regulated by incubation temperatures and by exogenous steroid hormones [4, 5]. In addition to determining sex, steroids have also been causally related to various physiological and behavioural actions in sea turtles. For example, corticosterone and testosterone have been associated with hepatic regulation and ovarian function during nesting activities in Caretta caretta [6–8]. Corticosterone concentration decreases when a turtle is subjected to stress or drops to low levels when a female turtle is breeding [9–11]. Nesting Lepidochelys olivacea during arribadas (mass nesting behaviour) maintain low corticosterone level as a mechanism of

References

[1]  M. Hau, R. E. Ricklefs, M. Wikelski, K. A. Lee, and J. D. Brawn, “Corticosterone, testosterone and life-history strategies of birds,” Proceedings of the Royal Society B. Biological Sciences, vol. 277, no. 1697, pp. 3203–3212, 2010.
[2]  E. J. Crespi, T. D. Williams, T. S. Jessop, and B. Delehanty, “Life history and the ecology of stress: how do glucocorticoid hormones influence life-history variation in animals?” Functional Ecology, vol. 27, no. 1, pp. 93–106, 2013.
[3]  D. Crews, J. Sakata, and T. Rhen, “Developmental effects on intersexual and intrasexual variation in growth and reproduction in a lizard with temperature-dependent sex determination,” Comparative Biochemistry and Physiology C: Pharmacology Toxicology and Endocrinology, vol. 119, no. 3, pp. 229–241, 1998.
[4]  T. Wibbels, J. J. Bull, and D. Crews, “Chronology and morphology of temperature-dependent sex determination.,” Journal of Experimental Zoology, vol. 260, no. 3, pp. 371–381, 1991.
[5]  D. Crews, A. R. Cantú, T. Rhen, and R. Vohra, “The relative effectiveness of estrone, estradiol-17β, and estriol in sex reversal in the red-eared slider (Trachemys scripta), a turtle with temperature-dependent sex determination,” General and Comparative Endocrinology, vol. 102, no. 3, pp. 317–326, 1996.
[6]  J. M. Whittier, F. Corrie, and C. Limpus, “Plasma steroid profiles in nesting loggerhead turtles (Caretta caretta) in Queensland, Australia: relationship to nesting episode and season,” General and Comparative Endocrinology, vol. 106, no. 1, pp. 39–47, 1997.
[7]  M. Hamann, T. S. Jessop, C. J. Limpus, and J. M. Whittier, “Interactions among endocrinology, seasonal reproductive cycles and the nesting biology of the female green sea turtle,” Marine Biology, vol. 140, no. 4, pp. 823–830, 2002.
[8]  M. Hamann, C. J. Limpus, and J. M. Whittier, “Patterns of lipid storage and mobilisation in the female green sea turtle (Chelonia mydas),” Journal of Comparative Physiology B, vol. 172, no. 6, pp. 485–493, 2002.
[9]  T. S. Jessop, N. N. FitzSimmons, C. J. Limpus, and J. M. Whittier, “Interactions between behavior and plasma steroids within the scramble mating system of the promiscuous green turtle, Chelonia mydas,” Hormones and Behavior, vol. 36, no. 2, pp. 86–97, 1999.
[10]  T. S. Jessop, C. J. Limpus, and J. M. Whittier, “Plasma steroid interactions during high-density green turtle nesting and associated disturbance,” General and Comparative Endocrinology, vol. 115, no. 1, pp. 90–100, 1999.
[11]  T. S. Jessop, “Modulation of the adrenocortical stress response in marine turtles (Cheloniidae): evidence for a hormonal tactic maximizing maternal reproductive investment,” Journal of Zoology, vol. 254, no. 1, pp. 57–65, 2001.
[12]  R. A. Valverde, D. W. Owens, D. S. MacKenzie, and S. M. Amoss Jr., “Basal and stress-induced corticosterone levels in olive Ridley sea turtles (Lepidochelys olivacea) in relation to their mass nesting behavior,” Journal of Experimental Zoology, vol. 284, pp. 652–662, 1999.
[13]  T. S. Jessop and M. Hamann, “Hormonal and metabolic responses to nesting activities in the green turtle, Chelonia mydas,” Journal of Experimental Marine Biology and Ecology, vol. 308, no. 2, pp. 253–267, 2004.
[14]  S. Wright, Samson Wright's Applied Physiology, Oxford University Press, Oxford, UK, 1984.
[15]  K. A. Bjorndal, “Nutritional ecology of sea turtles,” Copeia, pp. 736–751, 1985.
[16]  A. D. Tucker and M. A. Read, “Frequency of foraging by gravid green turtles (Chelonia mydas) at Raine Island, Great Barrier Reef,” Journal of Herpetology, vol. 35, no. 3, pp. 500–503, 2001.
[17]  K. Schmidt-Nielsen, “Energy metabolism,” in Animal Physiology, Adaptation and Environment, K. Schmidt-Nielsen, Ed., p. 612, Cambridge University Press, Cambridge, Mass, USA, 2004.
[18]  J. F. Leatherland, “Thyroid response to ovine thyrotropin challenge in cortisol- and dexamethasone-treated rainbow trout, Salmo gairdneri,” Comparative Biochemistry and Physiology A, vol. 86, no. 2, pp. 383–387, 1987.
[19]  C. J. Limpus, “The flatback turtle, Chelonia depressa Garman in southeast Queensland, Australia,” Herpetologica, vol. 27, pp. 431–446, 1971.
[20]  C. J. Limpus, C. J. Parmenter, R. Parker, and N. Ford, “The flatback turtle Chelonia depressa in Queensland the Peak Island rookery,” Herpetofauna, vol. 13, pp. 14–18, 1981.
[21]  D. W. Owens and G. J. Ruiz, “New methods of obtaining blood and cerebrospinal fluid from marine turtles,” Herpetologica, vol. 36, pp. 17–20, 1980.
[22]  A. B. Bolten, “Techniques for measuring sea turtles,” in Research and Management Techniques for the Conservation of Sea Turtles, K. L. Eckert, K. A. Bjorndal, F. A. Abreu-Grobois, and M. Donnelly, Eds., pp. 110–114, UCN/SSC: Marine Turtle Specialist Group, 1999.
[23]  K. Coufal and J. M. Whittier, “Identification of oestrone as a major oestrogenic steroid in marine turtle plasma as detected by HPLC. Short Communication,” in Proceedings of the 22nd Annual Symposium on Sea Turtle Biology and Conservation, J. A. Seminoff, Ed., NOAA Technical Memorandum NMFS-SEFSC 503, pp. 200–201, 2003.
[24]  C. E. Franklin, B. M. Davis, S. K. J. Peucker et al., “Comparison of stress induced by manual restraint and immobilisation in the estuarine crocodile, Crocodylus porosus,” Journal of Experimental Zoology A: Comparative Experimental Biology, vol. 298, no. 2, pp. 86–92, 2003.
[25]  M. P. Ikonomopoulou, Steroid hormones, steroid binding proteins and persistent environmental pollutants in green (Chelonia mydas) and flatback (Natator depressus) turtles [Ph.D. thesis], The University of Queensland, St Lucia, Australia, 2008.
[26]  R Core Team, R: A Language and Environment for Statistical Computing, R Foundation for Statistical Computing, Vienna, Austria, 2013, http://www.R-project.org/.
[27]  R. V. Lenth, “lsmeans: Least-squares means,” R package version 1.10-14, 2013, http://CRAN.R-project.org/package=lsmeans.
[28]  F. E. Harrell Jr., C. Dupont, et al., Hmisc: Harrell Miscellaneous, R Package Version 3.12-2, 2013, http://cran.r-project.org/web/packages/Hmisc/index.html.
[29]  W. N. Venables and B. D. Ripley, Modern Applied Statistics, Springer, New York, NY, USA, 2002.
[30]  C. J. Limpus, A Biological Review of Australian Marine Turtles, Queensland Government Environment Protection Agency, Brisbane, Australia, 2009.
[31]  C. J. Limpus, Conservation of Marine Turtles in the Indo-Pacific Region, Queensland Department of Environment and Heritage, Brisbane, Australia, 1995.
[32]  T. Wibbels, D. W. Owens, C. J. Limpus, P. C. Reed, and M. S. Amoss Jr., “Seasonal changes in serum gonadal steroids associated with migration, mating, and nesting in the loggerhead sea turtle (Caretta caretta),” General and Comparative Endocrinology, vol. 79, no. 1, pp. 154–164, 1990.
[33]  D. Gulko and K. Eckert, Eds., Sea Turtles: An Ecological Guide, Mutual Publishing, Honolulu, Hawaii, USA, 2004.
[34]  K. E. Arthur, Ecotoxicology of the cyanobacterium Lyngbya majuscula and health implications for green sea turtles (Chelonia mydas) [Ph.D. Thesis], The University of Queensland, Queensland, Australia, 2005.
[35]  C. J. Limpus, “A biological review of Australian marine turtle species, 5 Flatback turtle, Natator depressus (Garman),” Environmental Protection Agency, Brisbane, Australia, 2007.
[36]  T. Wibbels, D. W. Owens, P. Licht, C. Limpus, P. C. Reed, and M. S. Amoss Jr., “Serum gonadotropins and gonadal steroids associated with ovulation and egg production in sea turtles,” General and Comparative Endocrinology, vol. 87, no. 1, pp. 71–78, 1992.
[37]  P. Licht, W. Rainey, and K. Cliffton, “Serum gonadotropin and steroids associated with breeding activities in the green sea turtle, Chelonia mydas. II. Mating and nesting in natural populations,” General and Comparative Endocrinology, vol. 40, no. 1, pp. 116–122, 1980.
[38]  D. C. Rostal, J. S. Grumbles, K. S. Palmer, V. A. Lance, J. R. Spotila, and F. V. Paladino, “Changes in gonadal and adrenal steroid levels in the leatherback sea turtle (Dermochelys coriacea) during the nesting cycle,” General and Comparative Endocrinology, vol. 122, no. 2, pp. 139–147, 2001.
[39]  D. C. Rostal, D. W. Owens, J. S. Grumbles, D. S. MacKenzie, and M. S. Amoss Jr., “Seasonal reproductive cycle of the Kemp's ridley sea turtle (Lepidochelys kempi),” General and Comparative Endocrinology, vol. 109, no. 2, pp. 232–243, 1998.
[40]  M. P. Ikonomopoulou, A. J. Bradley, J. M. Whittier, and K. Ibrahim, “Identification and properties of steroid-binding proteins in nesting Chelonia mydas plasma,” Journal of Comparative Physiology B, vol. 176, no. 8, pp. 775–782, 2006.
[41]  J. R. Spotila, Sea Turtles: A Complete Guide to their Biology, Behavior, and Conservation, Johns Hopkins University Press, Baltimore, Md, USA, 1994.

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