INTRODUCTION Top

The loggerhead marine turtle (Caretta caretta) is distributed in worldwide subtropical regions (Pritchard 1997Pritchard P.C.H. 1997. Evolution, phylogeny, and current status. In: Lutz P.L., Musick J.A. (eds), The biology of sea turtles. CRC Press, Boca Raton, FL, pp. 1-28.). As with other marine turtle species (Meylan et al. 1990Meylan A.B., Bowen B.W., Avise J.C. 1990. A genetic test of the natal homing versus social facilitation models for green turtle migration. Science 248: 724-727.), this species is philopatric (Bowen et al. 1993Bowen B.W., Avise J.C., Richardson J.I., Meylan A., Margaritoulis D., Hopkins-Murphy S.R. 1993. Population structure of loggerhead turtles (Caretta caretta) in the Northwestern Atlantic Ocean and Mediterranean Sea. Conserv. Biol. 7: 834-844.), a behaviour that contrasts with this wide distribution (Bowen 2003Bowen B.W. 2003. What is a Loggerhead Turtle? The genetic perspective. In: Bolten A., Witherington B. (eds), Loggerhead Sea Turtles. Smithsonian Institution Press, Washington D.C. pp. 7-27.). As a consequence of natal homing, females generally return to nest to the beaches where they hatched, creating a spatial genetic structuring that can be easily detected using maternally inherited markers, such as those found in the mitochondrial DNA (mtDNA) (Bowen et al. 1993Bowen B.W., Avise J.C., Richardson J.I., Meylan A., Margaritoulis D., Hopkins-Murphy S.R. 1993. Population structure of loggerhead turtles (Caretta caretta) in the Northwestern Atlantic Ocean and Mediterranean Sea. Conserv. Biol. 7: 834-844., Laurent et al. 1993Laurent L., Lescure J., Excoffier L., Bowen B.W., Domingo M., Hadjichristophorou M., Kornaraky L., Trabucht G. 1993. Genetic studies of relationships between Mediterranean and Atlantic populations of loggerhead turtle Caretta caretta with a mitochondrial marker. Comptes Rendus de l’Académie des Sciences de la Vie. Sciences de la Vie, Paris 316: 1233-1239., Encalada et al. 1998Encalada S.E., Bjorndal K.A., Bolten A.B., Zurita J.C., Schroeder B., Possardt E., Sears C.J., Bowen B.W. 1998. Population structure of loggerhead turtle (Caretta caretta) nesting colonies in the Atlantic and Mediterranean as inferred from mitochondrial DNA control region sequences. Mar. Biol. 130: 567-575., Bowen et al. 2005Bowen B.W., Bass A.L., Soares L., Toonen R.J. 2005. Conservation implications of complex population structure: lessons from the loggerhead turtle (Caretta caretta). Mol. Ecol. 14: 2389-2402., Bowen and Karl 2007Bowen B.W., Karl S.A. 2007. Population genetics and phylogeography of sea turtles. Mol. Ecol. 16: 4886-4907., Carreras et al. 2007Carreras C., Pascual M., Cardona L., Aguilar A., Margaritoulis D., Rees A.F., Turkozan O., Levy Y., Gasith A., Aureggi M., Khalil M. 2007. The genetic structure of the loggerhead sea turtle (Caretta caretta) in the Mediterranean as revealed by nuclear and mitochondrial DNA and its conservation implications. Conserv. Genet. 8: 761-775., Lee 2008Lee P.L.M. 2008. Molecular ecology of marine turtles: New approaches and future directions. J. Exp. Mar. Biol. Ecol. 356: 25-42. ). The definition of these genetic management units (Moritz 1994Moritz C. 1994. Defining Evolutionarily Significant Units for Conservation. Trends Ecol. Evol. 9: 373-375.) is considered a milestone in conservation of these endangered animals (Hamann et al. 2010Hamann M., Godfrey M.H., Seminoff J.A., Arthur K., Barata P.C.R., Bjorndal K.A., Bolten A., Broderick A.C., Campbell L.M., Carreras C., Dutton P.H., Epperly S., Fitzsimmons N.N., Formia A., Girondot M., Hays G.C., Jiunn C.I., Kaska Y., Lewison R., Mortimer J.A., Nichols W.J., Reina R.D., Shanker K., Spotila J.R., Tomás J., Wallace B.P., Work T.M., Zbinden J.A., Godley B.J. 2010. Global research priorities for sea turtles: informing management and conservation in the 21st century. Endang. Species Res. 11: 245-269., Wallace et al. 2011Wallace B.P., DiMatteo A.D., Bolten A.B., Chaloupka M.Y., Hutchinson B.J., Abreu-Grobois F.A., Mortimer J.A., Seminoff J.A., Amorocho D., Bjorndal K.A., Bourjea J., Bowen B.W., Duenas R.B., Casale P., Choudhury B.C., Costa A., Dutton P.H., Fallabrino A., Finkbeiner E.M., Girard A., Girondot M., Hamann M., Hurley B.J., Lopez-Mendilaharsu M., Marcovaldi M.A., Musick J.A., Nel R., Pilcher N.J., Troeng S., Witherington B., Mast R.B. 2011. Global Conservation Priorities for Marine Turtles. PLoS One 6(9): e24510. ).

Furthermore, this genetic structuring has been used in the determination of the origin of turtles in feeding grounds. A loggerhead sea turtle may undertake vast migrations across the oceans during its life (Bowen et al. 1995Bowen B.W., Abreu-Grobois A., Balazs G.H., Kamezaki N., Limpus C.J., Ferl R.J. 1995. Trans-Pacific migrations of the loggerhead turtle (Caretta caretta) demonstrated with mitochondrial DNA markers. Proc. Natl. Acad. Sci. USA 92: 3731-3734., Bolten et al. 1998Bolten A.B., Bjorndal K.A., Martins H.R., Dellinger T., Biscoito M.J., Encalada S.E., Bowen B.W. 1998. Transatlantic developmental migrations of loggerhead sea turtles demonstrated by mtDNA sequence analysis. Ecol. Appl. 8: 1-7.). Thus, turtles produced at very different distant nesting sites might use the same feeding grounds during their development stages (Laurent et al. 1998Laurent L., Casale P., Bradai M.N., Godley B.J., Gerosa G., Broderick A.C., Schroth W., Schierwater B., Levy A.M., Freggi D., Abd El-Mawla E.M., Hadoud D.A., Gomati H.E., Domingo M., Hadjichristophorou M., Kornaraky L., Demirayak F., Gautier C. 1998. Molecular resolution of marine turtle stock composition in fishery bycatch: a case study in the Mediterranean. Mol. Ecol. 7: 1529-1542., Carreras et al. 2006Carreras C., Pont S., Maffucci F., Pascual M., Barcelo A., Bentivegna F., Cardona L., Alegre F., SanFelix M., Fernandez G., Aguilar A. 2006. Genetic structuring of immature loggerhead sea turtles (Caretta caretta) in the Mediterranean Sea reflects water circulation patterns. Mar. Biol. 149: 1269-1279., Maffucci et al. 2006Maffucci F., Kooistra W., Bentiveyna F. 2006. Natal origin of loggerhead turtles, Caretta caretta, in the neritic habitat off the Italian coasts, Central Mediterranean. Biol. Conserv. 127: 183-189.). Fisheries interactions in these feeding grounds are one of the major threats to the species (Carreras et al. 2004Carreras C., Cardona L., Aguilar A. 2004. Incidental catch of the loggerhead turtle Caretta caretta off the Balearic Islands (western Mediterranean). Biol. Conserv. 117: 321-329., Camiñas et al. 2006Camiñas J.A., Baez J.C., Valeiras X., Real R. 2006. Differential loggerhead by-catch and direct mortality due to surface longlines according to boat strata and gear type. Sci. Mar. 70: 661-665., Álvarez de Quevedo et al. 2010Álvarez de Quevedo I., Cardona L., De Haro A., Pubill E., Aguilar A. 2010. Sources of bycatch of loggerhead sea turtles in the western Mediterranean other than drifting longlines. ICES J. Mar. Sci. 67: 677-685., Baez et al. 2010Baez J.C., Real R., Macias D., de la Serna J.M., Bellido J.J., Camiñas J.A. 2010. Captures of swordfish Xiphias gladius (Linnaeus 1758) and loggerhead sea turtles Caretta caretta (Linnaeus 1758) associated with different bait combinations in the Western Mediterranean surface longline fishery. J. Appl. Ichthyol. 26: 126-127.), often resulting in high levels of mortality (Casale et al. 2007Casale P., Mazaris A.D., Freggi D., Basso R., Argano R. 2007. Survival probabilities of loggerhead sea turtles (Caretta caretta) estimated from capture-mark-recapture data in the Mediterranean Sea. Sci. Mar. 71: 365-372. , 2008bCasale P., Freggi D., Rocco M. 2008b. Mortality induced by drifting longline hooks and branchlines in loggerhead sea turtles, estimated through observation in captivity. Aquatic Conservation-Marine and Freshwater Ecosystems 18: 945-954.). Mixed stock analyses using mtDNA markers (Grant et al. 1980Grant W.S., Milner G.B., Krasnowski P., Utter F.M. 1980. Use of biochemical genetic variants for identification of Sockeye salmon (Oncorhynchus nerca) stocks in Cook Inlet, Alaska. Can. J. Fish. Aquat. Sci. 37: 1236-1247., Pella and Milner 1987Pella J.J., Milner G.B. 1987. Use of genetic marks in stock composition analysis. In Ryman N., Utter F. (eds), Population Genetics and Fishery Management. Univ. Washington Press, Seattle and London, pp. 247-276., Pella and Masuda 2001Pella J., Masuda M. 2001. Bayesian methods for analysis of stock mixtures from genetic characters. Fish. Bull. 99: 151-167., Bolker et al. 2007Bolker B.M., Okuyama T., Bjorndal K.A., Bolten A.B. 2007. Incorporating multiple mixed stocks in mixed stock analysis: ‘many-to-many’ analyses. Mol. Ecol. 16: 685-695.) have been used to assess relative impacts of threats (Bowen and Karl 2007Bowen B.W., Karl S.A. 2007. Population genetics and phylogeography of sea turtles. Mol. Ecol. 16: 4886-4907., Lee 2008Lee P.L.M. 2008. Molecular ecology of marine turtles: New approaches and future directions. J. Exp. Mar. Biol. Ecol. 356: 25-42.). Both the metapopulation genetic and mixed stock analyses are very sensitive to significant gaps of information in the description of the genetic signature of the nesting areas. For several nesting beaches, the sample size for genetic characterization is low in comparison with the numbers of adult females nesting there, while no samples at all have been collected for others.

The Mediterranean Sea hosts an independent regional management unit (Wallace et al. 2010Wallace B.P., DiMatteo A.D., Hurley B.J., Finkbeiner E.M., Bolten A.B., Chaloupka M.Y., Hutchinson B.J., Alberto Abreu-Grobois F., Amorocho D., Bjorndal K.A., Bourjea J., Bowen B.W., Briseno Duenas R., Casale P., Choudhury B.C., Costa A., Dutton P.H., Fallabrino A., Girard A., Girondot M., Godfrey M.H., Hamann M., Lopez-Mendilaharsu M., Marcovaldi M.A., Mortimer J.A., Musick J.A., Nel R., Pilcher N.J., Seminoff J.A., Troeng S., Witherington B., Mast R.B. 2010. Regional Management Units for Marine Turtles: A Novel Framework for Prioritizing Conservation and Research across Multiple Scales. PLoS One 5(12): e15465.) of loggerhead sea turtles, genetically separated from those in the Atlantic Ocean (Carreras et al. 2011Carreras C., Pascual M., Cardona L., Marco A., Bellido J.J., Castillo J.J., Tomás J., Raga J.A., Sanfelix M., Fernandez G., Aguilar A. 2011. Living Together but Remaining Apart: Atlantic and Mediterranean Loggerhead Sea Turtles (Caretta caretta) in Shared Feeding Grounds. J. Hered. 102: 666-677.). Although individuals are found at sea throughout the region, regular nesting is concentrated in the eastern basin (Broderick et al. 2002Broderick A.C., Glen F., Godley B.J., Hays G.C. 2002. Estimating the number of green and loggerhead turtles nesting annually in the Mediterranean. Oryx 36: 227-235., Margaritoulis et al. 2003Margaritoulis D., Argano R., Baran I., Bentivegna F., Bradai M.N., Cami-as J.A., Casale P., De Metrio G., Demetropoulos A., Gerosa G., Godley B.J., Hadoud D.A., Houghton J., Laurent L., Lazar B. 2003. Loggerhead Turtles in the Mediterranean Sea: Present Knowledge and Conservation Perspectives. In: Bolten A, Witherington BE (eds), Loggerhead Sea Turtles. Smithsonian Books, Washington D.C. pp. 175-198., Casale and Margaritoulis 2010Casale P., Margaritoulis D. 2010. Sea turtles in the Mediterranean: distribution, threats and conservation priorities. IUCN/SSC Marine Turtle Specialist Group, Gland, Switzerland ) with only sporadic nesting in the western basin (Delaugerre and Cesarini 2004Delaugerre M., Cesarini C. 2004. Confirmed nesting of the loggerhead turtle in Corsica. Marine Turtle Newsletter 104: 12., Bentivegna et al. 2008Bentivegna F., Treglia G., Hochscheid S. 2008. The first report of a loggerhead turtle Caretta caretta nest on the central Tyrrhenian coast (western Mediterranean). Mar. Biodiv. Rec. 1: 1-3., Tomás et al. 2008Tomás J., Gazo M., Alvarez C., Gozalbes P., Perdiguero D., Raga J.A., Alegre F. 2008. Is the Spanish coast within the regular nesting range of the Mediterranean loggerhead sea turtle (Caretta caretta)? J. Mar. Biol. Ass. U. K. 88: 1509-1512., Casale et al. 2012Casale P., Palilla G., Salemi A., Napoli A., Prinzi M., Genco L., Bonaviri D., Mastrogiacomo A., Oliverio M., Lo Valvo M. 2012. Exceptional sea turtle nest records in 2011 suggest an underestimated nesting potential in Sicily (Italy). Acta Herpetol. 7: 181-188.). Genetic studies of Mediterranean nesting populations started two decades ago, measuring restriction length polymorphisms (RLPFs) of the mtDNA (Bowen et al. 1993Bowen B.W., Avise J.C., Richardson J.I., Meylan A., Margaritoulis D., Hopkins-Murphy S.R. 1993. Population structure of loggerhead turtles (Caretta caretta) in the Northwestern Atlantic Ocean and Mediterranean Sea. Conserv. Biol. 7: 834-844., Laurent et al. 1993Laurent L., Lescure J., Excoffier L., Bowen B.W., Domingo M., Hadjichristophorou M., Kornaraky L., Trabucht G. 1993. Genetic studies of relationships between Mediterranean and Atlantic populations of loggerhead turtle Caretta caretta with a mitochondrial marker. Comptes Rendus de l’Académie des Sciences de la Vie. Sciences de la Vie, Paris 316: 1233-1239.). However, only one of those studies (Laurent et al. 1993Laurent L., Lescure J., Excoffier L., Bowen B.W., Domingo M., Hadjichristophorou M., Kornaraky L., Trabucht G. 1993. Genetic studies of relationships between Mediterranean and Atlantic populations of loggerhead turtle Caretta caretta with a mitochondrial marker. Comptes Rendus de l’Académie des Sciences de la Vie. Sciences de la Vie, Paris 316: 1233-1239.) sampled multiple nesting areas within the Mediterranean and suggested that internal structuring might exist. A fine scale sampling effort within Turkey confirmed this hypothesis at a local level (Schroth et al. 1996Schroth W., Streit B., Schierwater B. 1996. Evolutionary handicap for turtles. Nature 384: 521-522.). The sequencing of a 380-bp fragment of the hyper-variable region of the D-loop of the mtDNA and the increasing of sampled locations has markedly improved the knowledge of Mediterranean genetic structure and different management units (Moritz 1994Moritz C. 1994. Defining Evolutionarily Significant Units for Conservation. Trends Ecol. Evol. 9: 373-375.) were defined (Encalada et al. 1998Encalada S.E., Bjorndal K.A., Bolten A.B., Zurita J.C., Schroeder B., Possardt E., Sears C.J., Bowen B.W. 1998. Population structure of loggerhead turtle (Caretta caretta) nesting colonies in the Atlantic and Mediterranean as inferred from mitochondrial DNA control region sequences. Mar. Biol. 130: 567-575., Laurent et al. 1998Laurent L., Casale P., Bradai M.N., Godley B.J., Gerosa G., Broderick A.C., Schroth W., Schierwater B., Levy A.M., Freggi D., Abd El-Mawla E.M., Hadoud D.A., Gomati H.E., Domingo M., Hadjichristophorou M., Kornaraky L., Demirayak F., Gautier C. 1998. Molecular resolution of marine turtle stock composition in fishery bycatch: a case study in the Mediterranean. Mol. Ecol. 7: 1529-1542., Carreras et al. 2007Carreras C., Pascual M., Cardona L., Aguilar A., Margaritoulis D., Rees A.F., Turkozan O., Levy Y., Gasith A., Aureggi M., Khalil M. 2007. The genetic structure of the loggerhead sea turtle (Caretta caretta) in the Mediterranean as revealed by nuclear and mitochondrial DNA and its conservation implications. Conserv. Genet. 8: 761-775., Chaieb et al. 2010Chaieb O., Ouaer A.E., Maffucci F., Bradai M.N., Bentivegna F., Said K., Chatti N. 2010. Genetic survey of loggerhead sea turtle Caretta caretta nesting population in Tunisia. Marine Biodiversity Records 3: 1-6.). A recently designed set of primers (Abreu-Grobois et al. 2006Abreu-Grobois A., Horrocks J., Formia A., Leroux R., Velez-Zuazo X., Dutton P.H., Soares L., Meylan A., Browne D. 2006. New mtDNA d-loop primers which work for a variety of marine turtle species may increase the resolution capacity of mixed stock analysis. Proceedings of the 26th Annual Symposium on Sea Turtle Biology and Conservation, p. 179.) notably increased the length of the fragment sequenced, allowing enhanced description of management units, inter-population connections and genetic barriers within the Mediterranean (Yilmaz et al. 2011Yilmaz C., Turkozan O., Bardakci F. 2011. Genetic structure of loggerhead turtle (Caretta caretta) populations in Turkey. Biochem. Syst. Ecol. 39: 266-276., Saied et al. 2012Saied A., Maffucci F., Hochscheid S., Dryag S., Swayeb B., Borra M., Ouerghi A., Procaccini G., Bentivegna F. 2012. Loggerhead turtles nesting in Libya: an important management unit for the Mediterranean stock. Mar. Ecol. Prog. Ser. 450: 207-224., Clusa et al. 2013Clusa M., Carreras C., Pascual M., Demetropoulos A., Margaritoulis D., Rees A.F., Hamza A.A., Khalil M., Aureggi M., Levy Y., Turkozan O., Marco A., Aguilar A., Cardona L. 2013. Mitochondrial DNA reveals Pleistocenic colonisation of the Mediterranean by loggerhead turtles (Caretta caretta). J. Exp. Mar. Biol. Ecol. 439: 15-24.).

Despite these recent efforts, one notable omission from profiling using longer sequences is the breeding aggregation of Kyparissia Bay, which represents the second largest loggerhead nesting aggregation in the region (Margaritoulis et al. 2003Margaritoulis D., Argano R., Baran I., Bentivegna F., Bradai M.N., Cami-as J.A., Casale P., De Metrio G., Demetropoulos A., Gerosa G., Godley B.J., Hadoud D.A., Houghton J., Laurent L., Lazar B. 2003. Loggerhead Turtles in the Mediterranean Sea: Present Knowledge and Conservation Perspectives. In: Bolten A, Witherington BE (eds), Loggerhead Sea Turtles. Smithsonian Books, Washington D.C. pp. 175-198., Casale and Margaritoulis 2010Casale P., Margaritoulis D. 2010. Sea turtles in the Mediterranean: distribution, threats and conservation priorities. IUCN/SSC Marine Turtle Specialist Group, Gland, Switzerland). Genetic samples for this population remain limited to those 21 first published two decades ago in an RLPF study (Bowen et al. 1993Bowen B.W., Avise J.C., Richardson J.I., Meylan A., Margaritoulis D., Hopkins-Murphy S.R. 1993. Population structure of loggerhead turtles (Caretta caretta) in the Northwestern Atlantic Ocean and Mediterranean Sea. Conserv. Biol. 7: 834-844.) and sequenced later using the 380-bp primers (Encalada et al. 1998Encalada S.E., Bjorndal K.A., Bolten A.B., Zurita J.C., Schroeder B., Possardt E., Sears C.J., Bowen B.W. 1998. Population structure of loggerhead turtle (Caretta caretta) nesting colonies in the Atlantic and Mediterranean as inferred from mitochondrial DNA control region sequences. Mar. Biol. 130: 567-575.). Studies of other Greek aggregations using these primers suggested that western Greek sites could be grouped, as no differences were detected among them (Carreras et al. 2007Carreras C., Pascual M., Cardona L., Aguilar A., Margaritoulis D., Rees A.F., Turkozan O., Levy Y., Gasith A., Aureggi M., Khalil M. 2007. The genetic structure of the loggerhead sea turtle (Caretta caretta) in the Mediterranean as revealed by nuclear and mitochondrial DNA and its conservation implications. Conserv. Genet. 8: 761-775.). However, the extra length of the new sequences is highly polymorphic (Monzon-Arguello et al. 2010Monzon-Arguello C., Rico C., Naro-Maciel E., Varo-Cruz N., Lopez P., Marco A., Lopez-Jurado L.F. 2010. Population structure and conservation implications for the loggerhead sea turtle of the Cape Verde Islands. Conserv. Genet. 11: 1871-1884.) and haplotypes that are common among different nesting areas often split into different regional variants thus increasing the power to detect differentiation among populations (Monzon-Arguello et al. 2010Monzon-Arguello C., Rico C., Naro-Maciel E., Varo-Cruz N., Lopez P., Marco A., Lopez-Jurado L.F. 2010. Population structure and conservation implications for the loggerhead sea turtle of the Cape Verde Islands. Conserv. Genet. 11: 1871-1884., Shamblin et al. 2012Shamblin B.M., Bolten A.B., Bjorndal K.A., Dutton P.H., Nielsen J.T., Abreu-Grobois F.A., Reich K.J., Witherington B.E., Bagley D.A., Ehrhart L.M., Tucker A.D., Addison D.S., Arenas A., Johnson C., Carthy R.R., Lamont M.M., Dodd M.G., Gaines M.S., LaCasella E., Nairn C.J. 2012. Expanded mitochondrial control region sequences increase resolution of stock structure among North Atlantic loggerhead turtle rookeries. Mar. Ecol. Prog. Ser. 469: 145-160. , Clusa et al. 2013Clusa M., Carreras C., Pascual M., Demetropoulos A., Margaritoulis D., Rees A.F., Hamza A.A., Khalil M., Aureggi M., Levy Y., Turkozan O., Marco A., Aguilar A., Cardona L. 2013. Mitochondrial DNA reveals Pleistocenic colonisation of the Mediterranean by loggerhead turtles (Caretta caretta). J. Exp. Mar. Biol. Ecol. 439: 15-24.). For instance, two nesting areas in Libya that were indistinguishable using short fragments became significantly different using the longer ones (Saied et al. 2012Saied A., Maffucci F., Hochscheid S., Dryag S., Swayeb B., Borra M., Ouerghi A., Procaccini G., Bentivegna F. 2012. Loggerhead turtles nesting in Libya: an important management unit for the Mediterranean stock. Mar. Ecol. Prog. Ser. 450: 207-224.). Thus, it is clear that the relationship of the important nesting beach of Kyparissia within the Mediterranean needs to be elaborated using the new sequences. This will complete the knowledge of genetic structuring within the region and will inform an important part of the baseline for future MSA analysis.

In this study, we analysed the mtDNA diversity of the Kyparissia Bay nesting population using the 800-bp fragment with a primer set that includes the traditional 380-bp mtDNA fragment (Abreu-Grobois et al. 2006Abreu-Grobois A., Horrocks J., Formia A., Leroux R., Velez-Zuazo X., Dutton P.H., Soares L., Meylan A., Browne D. 2006. New mtDNA d-loop primers which work for a variety of marine turtle species may increase the resolution capacity of mixed stock analysis. Proceedings of the 26th Annual Symposium on Sea Turtle Biology and Conservation, p. 179.) and we compared the results obtained with haplotype frequencies obtained from the available published literature. The objectives of this study were to a) characterize the mtDNA diversity of the Kyparissia nesting population, b) to define the degree of genetic differentiation between the Kyparissia and the other nesting populations and c) to test whether the use of longer sequences and the inclusion of Kyparissia Bay changes the previously defined genetic structuring within the Mediterranean.

MATERIALS AND METHODSTop

Samples from the Kyparissia Bay nesting area (KYP, Fig. 1) were collected during the 2012 nesting season. Skin plug samples were collected from loggerhead (C. caretta) nesting females, during the covering phase, after egg deposition. Pseudoreplication was avoided by taking only one sample from each uniquely identified, tagged nesting turtle. Samples were stored in 90% ethanol.

We amplified a long (~800 bp) fragment of the mitochondrial DNA (mtDNA) control region using the primers LCM15382 (5’-GCTTAACCCTAAAGCATTGG-3’) and H950 (5’-GTCTCGGATTTAGGGGTTT-3’) (Abreu-Grobois et al. 2006Abreu-Grobois A., Horrocks J., Formia A., Leroux R., Velez-Zuazo X., Dutton P.H., Soares L., Meylan A., Browne D. 2006. New mtDNA d-loop primers which work for a variety of marine turtle species may increase the resolution capacity of mixed stock analysis. Proceedings of the 26th Annual Symposium on Sea Turtle Biology and Conservation, p. 179.), which includes the short region (~380 bp) historically surveyed for several marine turtle species in previous studies (Encalada et al. 1998Encalada S.E., Bjorndal K.A., Bolten A.B., Zurita J.C., Schroeder B., Possardt E., Sears C.J., Bowen B.W. 1998. Population structure of loggerhead turtle (Caretta caretta) nesting colonies in the Atlantic and Mediterranean as inferred from mitochondrial DNA control region sequences. Mar. Biol. 130: 567-575., Laurent et al. 1998Laurent L., Casale P., Bradai M.N., Godley B.J., Gerosa G., Broderick A.C., Schroth W., Schierwater B., Levy A.M., Freggi D., Abd El-Mawla E.M., Hadoud D.A., Gomati H.E., Domingo M., Hadjichristophorou M., Kornaraky L., Demirayak F., Gautier C. 1998. Molecular resolution of marine turtle stock composition in fishery bycatch: a case study in the Mediterranean. Mol. Ecol. 7: 1529-1542., Carreras et al. 2007Carreras C., Pascual M., Cardona L., Aguilar A., Margaritoulis D., Rees A.F., Turkozan O., Levy Y., Gasith A., Aureggi M., Khalil M. 2007. The genetic structure of the loggerhead sea turtle (Caretta caretta) in the Mediterranean as revealed by nuclear and mitochondrial DNA and its conservation implications. Conserv. Genet. 8: 761-775., Chaieb et al. 2010Chaieb O., Ouaer A.E., Maffucci F., Bradai M.N., Bentivegna F., Said K., Chatti N. 2010. Genetic survey of loggerhead sea turtle Caretta caretta nesting population in Tunisia. Marine Biodiversity Records 3: 1-6.). Extraction and amplification were conducted using the Phire® Animal Tissue Direct PCR Kit (Finnzymes) following the manufacturer’s specifications. Each 50-μl reaction contained 0.5 mm of the sample skin, 1× Phire® Animal Tissue PCR Buffer, 0.5 μM of each primer and 1 μL of Phire® Hot Start II DNA Polymerase. After an initial 5 min denaturing step (98°C), our PCR protocol consisted of 40 cycles of the following temperature regime: 5 s at 98°C (denaturing), 5 s at 60.6°C (annealing) and 20 s at 72°C (extension). In addition, we included a final extension step of 1 min at 72°C. The resulting PCR product were visualized in agarose gel and we removed single-stranded DNA by digesting 45 μL of PCR product with 9 μL of a combined Exonuclease I and Shrimp Alkaline Phosphatase solution (ExoSAP®). The reaction was incubated for 30 min at 37°C, followed by 10 min incubation at 80°C to inactivate the two enzymes. We sequenced both forward and reverse strands using a 3730XL Automatic Sequencer (Macrogen Inc. sequencing service). Sequences were aligned using Geneious v5.5 (Drummond et al. 2011Drummond A.J., Ashton B., Buxton S., Cheung M., Cooper A., Heled J., Moir R., Stones-Havas S., Sturrock S., Thierer T., Wilson A. 2011. Geneious v5.5 created by Biomatters. Available from http://www.geneious.com) or BioEdit v7.1.11 (Hall 1999Hall T.A. 1999. BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symposium Series 41: 95-98.) and compared with known loggerhead haplotypes found in the database maintained by the Archie Carr Center for Sea Turtle Research (http://accstr.ufl.edu/), which includes all published long and short haplotypes.

We reviewed all published long (~800 bp) and short (~380 bp) mtDNA haplotype frequencies in Mediterranean nesting areas (Fig. 1). When different sample sets were available from the same location, we used only the one with the highest number of samples in order to avoid pseudoreplication. Only sample sets with at least 10 samples were considered for the analysis. Finally, sample sets covering an area that has been demonstrated to include genetically different units were also discarded. In order to assess the genetic diversity of Kyparissia compared with the other Mediterranean nesting sites, we calculated haplotype diversity (h) and nucleotide diversity (π) (Nei 1982Nei M. 1982. Evolution of Human Races at the Gene Level. In: Bonne-Tamir B., Cohen T., Goodman R.M. (eds), Human Genetics Part A: The Unfolding Genome. Alan R. Liss, New York, pp. 167-181.) of each population using the program Arlequin 5.1 (Excoffier et al. 2005Excoffier L., Laval G., Schneider S. 2005. Arlequin (version 3.0): An integrated software package for population genetics data analysis. Evol. Bioinform. 1: 47-50.). Fu’s Fs neutrality test for the detection of population growth (Fu 1997Fu Y.X. 1997. Statistical tests of neutrality of mutations against population growth, hitchhiking and background selection. Genetics 147: 915-925.) was undertaken with the DnaSP software package (Rozas et al. 2003Rozas J., Sanchez-DelBarrio J.C., Messeguer X., Rozas R. 2003. DnaSP, DNA polymorphism analyses by the coalescent and other methods. Bioinf. 19: 2496-2497.). Fs tends to be negative under an excess of recent mutations and a significant negative value was taken as evidence of recent population expansion. Differentiation among population pairs was assessed considering genetic distances (Φ_st). Significance of differentiation was also tested by computing the exact test, based on haplotype frequencies (Goudet et al. 1996Goudet J., Raymond M., de Meeüs T. 1996. Testing differentiation in diploid populations. Genetics 144: 1931-1938.) and by chi-square tests, in which values were compared with the distributions observed by randomizing individuals among populations using Monte-Carlo resampling (Rolf and Bentzen 1989Rolf D.A., Bentzen P. 1989. The statistical analysis of mitochondrial DNA polymorphisms: X² and the problem of small samples. Mol. Biol. Evol. 6: 539-545). We also performed a locus by locus analysis of AMOVA in order to detect which polymorphisms of the sequence were more informative. All these analyses were performed using Arlequin 5.1 (Excoffier et al. 2005Excoffier L., Laval G., Schneider S. 2005. Arlequin (version 3.0): An integrated software package for population genetics data analysis. Evol. Bioinform. 1: 47-50.). Genetic distances were used to perform a principal coordinate analysis (PCA) with the package GenAlEX 6.2 (Peakall and Smouse 2006Peakall R., Smouse P.E. 2006. GENALEX 6: genetic analysis in Excel. Population genetic software for teaching and research. Mol. Ecol. Notes 6: 288-295.) and a UPGMA consensus tree was build using the software TFPGA 1.3 as a result of 1000 permutations (Miller 1997Miller M. 1997. Tools for population genetic analyses (TFPGA) 1.3; a Windows program for the analysis of allozyme and molecular population genetic data. Documentation file. Available at: http://www.marksgeneticsoftware.net/tfpga.htm.). A sequential Bonferroni correction was not applied for multiple pairwise comparisons, since they dramatically increase the probability for type II error (β: assume no differentiation when it does exist), an effect that becomes worse as many p-values are discarded (Perneger 1998Perneger T.V. 1998. What’s wrong with Bonferroni adjustments. British Med. J. 316: 1236-1238., Cabin and Mitchell 2000Cabin R.J., Mitchell R.J. 2000. To Bonferroni or not to bonferroni: when and how are the questions. Bull. Ecol. Soc. Am. 81: 246-248., Moran 2003Moran M.D. 2003. Arguments for rejecting the sequential Bonferroni in ecological studies. Oikos 100: 403-405.). However, we included a false discovered rate (FDR) correction that calculates the most appropriate threshold for the P-value significance considering the multiple comparisons involved in the analysis under an expected original threshold of P<0.05 (Narum 2006Narum S.R. 2006. Beyond Bonferroni: Less conservative analyses for conservation genetics. Conserv. Genet. 7: 783-787.).

Finally, we used the program POWSIM 4.1 (Ryman and Palm 2006Ryman N., Palm S. 2006. POWSIM: a computer program for assessing statistical power when testing for genetic differentiation. Mol. Ecol. Notes 6: 600-602.) to evaluate the statistical power of the long (~800 bp) mtDNA marker in the Mediterranean. Statistical power is defined as the probability of rejecting H₀, thus accepting H₁ (no differentiation among populations), and is an essential complement to assess the reliability of the non-significant pairwise comparisons. The program simulates the divergence of different populations and estimates the probability of false negatives by resampling them. Thus, statistical power is expressed as the proportion of non-significant outcomes (1000 replicates) of the diverged populations. We simulated different levels of divergence (F_st) by fixing the number of effective population size (Ne) at 500 and modifying the number of generations of divergence (t) (Ryman et al. 2006Ryman N., Palm S., Andre C., Carvalho G.R., Dahlgren T.G., Jorde P.E., Laikre L., Larsson L.C., Palme A., Ruzzante D.E. 2006. Power for detecting genetic divergence: differences between statistical methods and marker loci. Mol. Ecol. 15: 2031-2045.). We determined the statistical power of our marker by considering sample sizes of 10, 20, 30, 50 and 100, thus covering the range of sample sizes from Mediterranean nesting beaches, and adjusting the program for organelle (mtDNA) data (Larsson et al. 2009Larsson L.C., Charlier J., Laikre L., Ryman N. 2009. Statistical power for detecting genetic divergence-organelle versus nuclear markers. Conserv. Genet. 10: 1255-1264.).

RESULTSTop

A total of 36 sequences were obtained from females at the Kyparissia Bay nesting aggregation, and three haplotypes were found, when either the short or the long fragment was considered. These haplotypes were the widespread CC-A2/CC-A2.1 (Genebank EU179445, (Shamblin et al. 2012Shamblin B.M., Bolten A.B., Bjorndal K.A., Dutton P.H., Nielsen J.T., Abreu-Grobois F.A., Reich K.J., Witherington B.E., Bagley D.A., Ehrhart L.M., Tucker A.D., Addison D.S., Arenas A., Johnson C., Carthy R.R., Lamont M.M., Dodd M.G., Gaines M.S., LaCasella E., Nairn C.J. 2012. Expanded mitochondrial control region sequences increase resolution of stock structure among North Atlantic loggerhead turtle rookeries. Mar. Ecol. Prog. Ser. 469: 145-160.)), the Greek haplotype CC-A6/CC-A6.1 (Genebank JQ350705, (Yilmaz et al. 2012Yilmaz C., Turkozan O., Bardakci F., White M., Kararaj E. 2012. Loggerhead turtles (Caretta caretta) foraging at Drini Bay in Northern Albania: Genetic characterisation reveals new haplotypes. Acta Herpetol. 7: 155-162., Clusa et al. 2013Clusa M., Carreras C., Pascual M., Demetropoulos A., Margaritoulis D., Rees A.F., Hamza A.A., Khalil M., Aureggi M., Levy Y., Turkozan O., Marco A., Aguilar A., Cardona L. 2013. Mitochondrial DNA reveals Pleistocenic colonisation of the Mediterranean by loggerhead turtles (Caretta caretta). J. Exp. Mar. Biol. Ecol. 439: 15-24.)) and the haplotype CC-A31/CC-A31.1 (Genebank AM949678, (Garofalo et al. 2009Garofalo L., Mingozzi T., Mico A., Novelletto A. 2009. Loggerhead turtle (Caretta caretta) matrilines in the Mediterranean: further evidence of genetic diversity and connectivity. Mar. Biol. 156: 2085-2095.)), previously found only in Calabria (Italy; Tables 1 and 2). The Kyparissia Bay nesting area showed moderate levels of variability compared with the other Mediterranean nesting populations (Table 3) and no recent expansion was suggested irrespective of the length of the marker (Fu’s Fs neutrality test P<0.05 in both cases).

With the addition of our results, we compiled a total of 676 individuals with genetic information for the short fragment and 546 individuals with genetic information for the long fragment (Tables 1, 2). After filtering the data to avoid pseudoreplication, we had 535 samples from 16 nesting populations for the short fragment and 519 samples from 15 nesting populations for the long fragment, since the Tunisia nesting population has only been analysed with short sequences (Tables 1, 2). The long fragment showed deeper differentiation (8 of 14 significant values) between Kyparissia Bay and other Mediterranean nesting areas than the short one (6 of 15 significant values; Table 3). The Kyparissia Bay nesting population was not different to the other western Greek nesting populations (Lakonikos Bay and Zakynthos) when either short or long fragments were compared (Table 3) and was also grouped with these populations by the UPGMA tree with a 64% bootstrap value (Fig. 2). Considering these results and the fact that the three nesting areas exhibited the Greek haplotype CC-A6.1 and the common haplotype CC-A2.1 in similar proportions we grouped them as western Greece (WGR) for subsequent analysis.

Once WGR had been grouped (Table 4), the long fragment showed a much deeper differentiation among rookeries (63 of 78 significant values) than the short fragment (51 of 91 significant values). These differences were more pronounced in those populations in which the short haplotype CC-A2 splits into different long haplotypes, CC-A2.1, CC-A2.8 and CC-A2.9 (SIR, MIS, CRE, ISR). Western Greece was significantly different to all other populations with the exception of Misurata (Libya) using long fragments. The differences between the results from long and short fragments were also reflected in the PCA analysis, where the relative position of the populations where the CC-A2 haplotype splits into two or more variants (SIR, MIS, CRE, ISR) were much clearer along the second principal coordinate (Fig. 3). This finding was confirmed by the locus-by-locus AMOVA, which showed that the extended fragment has three polymorphic sites, two of them very informative (Fig. 4), which correspond to the sites differentiating these haplotypes (locus 121 separates CC-A2.9 from CC-A2.1 and locus 743 separates CC-A2.8 from CC-A2.1). The remaining 12 polymorphic sites were within the short sequence previously analysed.

The analysis of statistical power showed that the long mtDNA marker had low power in detecting low differentiation (e.g. F_st<0.01) but high power in detecting high differentiation (e.g. F_st<0.04) (Fig. 5). The statistical power in detecting intermediate divergence values was highly dependent on sample size, although a sample size of n=10 always yielded low statistical power, even at high differentiation levels. The results were very similar when the chi-square or the exact test were used, although the latter had slightly more power.

DISCUSSIONTop

The present study confirmed the findings of previous work (Monzon-Arguello et al. 2010Monzon-Arguello C., Rico C., Naro-Maciel E., Varo-Cruz N., Lopez P., Marco A., Lopez-Jurado L.F. 2010. Population structure and conservation implications for the loggerhead sea turtle of the Cape Verde Islands. Conserv. Genet. 11: 1871-1884., Shamblin et al. 2012Shamblin B.M., Bolten A.B., Bjorndal K.A., Dutton P.H., Nielsen J.T., Abreu-Grobois F.A., Reich K.J., Witherington B.E., Bagley D.A., Ehrhart L.M., Tucker A.D., Addison D.S., Arenas A., Johnson C., Carthy R.R., Lamont M.M., Dodd M.G., Gaines M.S., LaCasella E., Nairn C.J. 2012. Expanded mitochondrial control region sequences increase resolution of stock structure among North Atlantic loggerhead turtle rookeries. Mar. Ecol. Prog. Ser. 469: 145-160., Clusa et al. 2013Clusa M., Carreras C., Pascual M., Demetropoulos A., Margaritoulis D., Rees A.F., Hamza A.A., Khalil M., Aureggi M., Levy Y., Turkozan O., Marco A., Aguilar A., Cardona L. 2013. Mitochondrial DNA reveals Pleistocenic colonisation of the Mediterranean by loggerhead turtles (Caretta caretta). J. Exp. Mar. Biol. Ecol. 439: 15-24.) that indicated that the new set of primers improves the resolution of population structuring of the loggerhead turtle within the Mediterranean. This improvement is uneven, as it relies on the split of the common CC-A2 haplotype into a widespread haplotype (CC-A2.1) and several regional variants (CC-A2.8 and CC-A2.9) caused by two very informative polymorphic sites outside the short region. Thus, all populations including one of these regional CC-A2 variants (Sirte, Misurata, Crete and Israel) resulted in a higher differentiation level detected with other Mediterranean nesting populations, either using common Φ_st statistics or the PCA. As a consequence, we strongly recommend the use of this new set of primers in future loggerhead turtle genetic studies, especially for foraging areas where information is thus far only available for the short fragment.

The nesting area of Kyparissia Bay represents almost 9% of total nesting in the Mediterranean, considering that recent estimates suggested a reproductive output of approximately 7200 nests per year for the region (Casale and Margaritoulis 2010Casale P., Margaritoulis D. 2010. Sea turtles in the Mediterranean: distribution, threats and conservation priorities. IUCN/SSC Marine Turtle Specialist Group, Gland, Switzerland.), although data of some places may be incomplete. Our study confirmed the genetic differentiation between nesters at this important nesting area and most of the other nesting areas in the Mediterranean, especially when the newer, longer markers were considered. However, it also confirmed the grouping of Kyparissia Bay with both Zakynthos and Lakonikos Bay as an independent genetic unit, as suggested in previous studies with shorter markers (Carreras et al. 2007Carreras C., Pascual M., Cardona L., Aguilar A., Margaritoulis D., Rees A.F., Turkozan O., Levy Y., Gasith A., Aureggi M., Khalil M. 2007. The genetic structure of the loggerhead sea turtle (Caretta caretta) in the Mediterranean as revealed by nuclear and mitochondrial DNA and its conservation implications. Conserv. Genet. 8: 761-775.). This grouping is supported by other lines of evidence, as tagging studies have demonstrated interchange of females between these nesting areas (Margaritoulis 1998Margaritoulis D. 1998. Interchange of nesting loggerheads among Greek beaches. In: Epperly S., Braun-McNeill J. (eds), Proceedings of the seventeenth annual sea turtle symposium. NOAA Technical Memorandum, National Marine Fisheries Service, Southeast Fisheries Science Center, Orlando, Florida, pp. 225-227.), even within the same nesting season (Margaritoulis D, unpublished data). The three nesting areas included in the western Greece group produced more than 2000 nests per year on average, which is around one quarter of all Mediterranean nesting production.

As a consequence of this grouping, the overall structuring of Mediterranean nesting areas resulting from our study did not change significantly in relation to previous studies using the long fragment (Clusa et al. 2013Clusa M., Carreras C., Pascual M., Demetropoulos A., Margaritoulis D., Rees A.F., Hamza A.A., Khalil M., Aureggi M., Levy Y., Turkozan O., Marco A., Aguilar A., Cardona L. 2013. Mitochondrial DNA reveals Pleistocenic colonisation of the Mediterranean by loggerhead turtles (Caretta caretta). J. Exp. Mar. Biol. Ecol. 439: 15-24.). However, the increased sampling of this western Greece group increased the degree of differentiation detected between this and the populations of Cyprus, mid-Turkey, Lebanon and eastern Turkey, thus confirming its isolation and status as an independent management unit. Misurata (Libya) was the only population that did not differ from western Greece, but this population showed a low degree of differentiation with almost all Mediterranean nesting populations, probably because of the low sample size of the molecular data defining it. The authors who analysed this population recognized that this low sample size could affect the ability to detect differentiation (Saied et al. 2012Saied A., Maffucci F., Hochscheid S., Dryag S., Swayeb B., Borra M., Ouerghi A., Procaccini G., Bentivegna F. 2012. Loggerhead turtles nesting in Libya: an important management unit for the Mediterranean stock. Mar. Ecol. Prog. Ser. 450: 207-224.), although they did not test it. Our statistical power analysis clearly shows that sample sizes below 20 might fail when detecting differentiation and thus higher numbers are desirable, and this could explain why all but one non-significant value involve one of the two populations with the lowest sample size (Misurata and Lebannon).

Many genetic studies have been conducted in the Mediterranean nesting beaches over the last two decades (Encalada et al. 1998Encalada S.E., Bjorndal K.A., Bolten A.B., Zurita J.C., Schroeder B., Possardt E., Sears C.J., Bowen B.W. 1998. Population structure of loggerhead turtle (Caretta caretta) nesting colonies in the Atlantic and Mediterranean as inferred from mitochondrial DNA control region sequences. Mar. Biol. 130: 567-575., Laurent et al. 1998Laurent L., Casale P., Bradai M.N., Godley B.J., Gerosa G., Broderick A.C., Schroth W., Schierwater B., Levy A.M., Freggi D., Abd El-Mawla E.M., Hadoud D.A., Gomati H.E., Domingo M., Hadjichristophorou M., Kornaraky L., Demirayak F., Gautier C. 1998. Molecular resolution of marine turtle stock composition in fishery bycatch: a case study in the Mediterranean. Mol. Ecol. 7: 1529-1542., Carreras et al. 2007Carreras C., Pascual M., Cardona L., Aguilar A., Margaritoulis D., Rees A.F., Turkozan O., Levy Y., Gasith A., Aureggi M., Khalil M. 2007. The genetic structure of the loggerhead sea turtle (Caretta caretta) in the Mediterranean as revealed by nuclear and mitochondrial DNA and its conservation implications. Conserv. Genet. 8: 761-775., Garofalo et al. 2009Garofalo L., Mingozzi T., Mico A., Novelletto A. 2009. Loggerhead turtle (Caretta caretta) matrilines in the Mediterranean: further evidence of genetic diversity and connectivity. Mar. Biol. 156: 2085-2095., Chaieb et al. 2010Chaieb O., Ouaer A.E., Maffucci F., Bradai M.N., Bentivegna F., Said K., Chatti N. 2010. Genetic survey of loggerhead sea turtle Caretta caretta nesting population in Tunisia. Marine Biodiversity Records 3: 1-6., Yilmaz et al. 2012Yilmaz C., Turkozan O., Bardakci F., White M., Kararaj E. 2012. Loggerhead turtles (Caretta caretta) foraging at Drini Bay in Northern Albania: Genetic characterisation reveals new haplotypes. Acta Herpetol. 7: 155-162., Saied et al. 2012Saied A., Maffucci F., Hochscheid S., Dryag S., Swayeb B., Borra M., Ouerghi A., Procaccini G., Bentivegna F. 2012. Loggerhead turtles nesting in Libya: an important management unit for the Mediterranean stock. Mar. Ecol. Prog. Ser. 450: 207-224., Clusa et al. 2013Clusa M., Carreras C., Pascual M., Demetropoulos A., Margaritoulis D., Rees A.F., Hamza A.A., Khalil M., Aureggi M., Levy Y., Turkozan O., Marco A., Aguilar A., Cardona L. 2013. Mitochondrial DNA reveals Pleistocenic colonisation of the Mediterranean by loggerhead turtles (Caretta caretta). J. Exp. Mar. Biol. Ecol. 439: 15-24.), sometimes resulting in the production of several sample sets for the same locations. The risk of pseudoreplication between different sample sets is very high, especially in view of the small population sizes of some of the nesting beaches. Thus, although all studies took precautions to avoid pseudoreplication of their samples, a filtering process like the one conducted in this study has to be used when different studies of the same location are considered. However, this filtering process has some shortcomings. Firstly, we have shown that statistical power to detect differentiation decreases as the total number of samples decreases. For instance, a total of 25 samples were analysed from Israel and a total of 69 samples were analysed from Sirte, Libya. However, after filtering, only 19 for Israel or 35 for Sirte were used for the analysis. Secondly, some exclusive haplotypes have been found by chance only in sample sets that were not optimal considering the filtering criteria. It is noteworthy that the haplotype CC-A10 has been found in the Mediterranean only in a Greek sample set of ten samples (Table 1). By discarding this sample set, we are ignoring that this haplotype is present not only in Greece but also in the whole Mediterranean Sea. A similar issue can be seen in two of the three sample sets of Sirte (Libya), one with the single sample with a CC-A65.1 and the other with the single sample with a CC-A68 found in the whole Mediterranean (Table 1).

The existence of orphan haplotypes (haplotypes not detected in nesting areas but in feeding grounds) is one of the shortcomings of the mixed stock analysis and leads to mis-assignations. For instance, several individuals exhibiting the CC-A10 haplotype have been found in feeding grounds within the Mediterranean Sea, such as northeastern Spain (Carreras et al. 2006Carreras C., Pont S., Maffucci F., Pascual M., Barcelo A., Bentivegna F., Cardona L., Alegre F., SanFelix M., Fernandez G., Aguilar A. 2006. Genetic structuring of immature loggerhead sea turtles (Caretta caretta) in the Mediterranean Sea reflects water circulation patterns. Mar. Biol. 149: 1269-1279.), the Alboran region (Revelles et al. 2007Revelles M., Carreras C., Cardona L., Marco A., Bentivegna F., Castillo J.J., De Martino G., Mons J.L., Smith M.B., Rico C., Pascual M., Aguilar A. 2007. Evidence for an asymmetrical size exchange of loggerhead sea turtles between the Mediterranean and the Atlantic through the Straits of Gibraltar. J. Exp. Mar. Biol. Ecol. 349: 261-271.), the northern Tunisian Coast, and the Gulf of Gabes (Chaieb et al. 2012Chaieb O., Elouaer A., Maffucci F., Karaa S., Bradai M.N., ElHili H., Bentivegna F., Said K., Chatti N. 2012. Population structure and dispersal patterns of loggerhead sea turtles Caretta caretta in Tunisian coastal waters, central Mediterranean. Endang. Species Res. 18: 35-45.). Thus, although a filtering process is always desirable to avoid pseudoreplication problems in population genetic studies (like the present study), its application in future mixed stock analysis should be carefully considered. Considering the pros and cons of each approach, some studies in the past have pooled all samples available from nesting areas (Carreras et al. 2006Carreras C., Pont S., Maffucci F., Pascual M., Barcelo A., Bentivegna F., Cardona L., Alegre F., SanFelix M., Fernandez G., Aguilar A. 2006. Genetic structuring of immature loggerhead sea turtles (Caretta caretta) in the Mediterranean Sea reflects water circulation patterns. Mar. Biol. 149: 1269-1279., Maffucci et al. 2006Maffucci F., Kooistra W., Bentiveyna F. 2006. Natal origin of loggerhead turtles, Caretta caretta, in the neritic habitat off the Italian coasts, Central Mediterranean. Biol. Conserv. 127: 183-189., Casale et al. 2008aCasale P., Freggi D., Gratton P., Argano R., Oliverio M. 2008a. Mitochondrial DNA reveals regional and interregional importance of the central Mediterranean African shelf for loggerhead sea turtles (Caretta caretta). Sci. Mar. 72: 541-548., Chaieb et al. 2012Chaieb O., Elouaer A., Maffucci F., Karaa S., Bradai M.N., ElHili H., Bentivegna F., Said K., Chatti N. 2012. Population structure and dispersal patterns of loggerhead sea turtles Caretta caretta in Tunisian coastal waters, central Mediterranean. Endang. Species Res. 18: 35-45.), while others used only the best available sample set per site (Monzon-Arguello et al. 2009Monzon-Arguello C., Rico C., Carreras C., Calabuig P., Marco A., Lopez-Jurado L.F. 2009. Variation in spatial distribution of juvenile loggerhead turtles in the eastern Atlantic and western Mediterranean Sea. J. Exp. Mar. Biol. Ecol. 373: 79-86., Giovannotti et al. 2010Giovannotti M., Franzellitti S., Cerioni P.N., Fabbri E., Guccione S., Vallini C., Tinti F., Caputo V. 2010. Genetic characterization of loggerhead turtle (Caretta caretta) individuals stranded and caught as bycatch from the North-Central Adriatic Sea. Amphibia-Reptilia 31: 127-133., Carreras et al. 2011Carreras C., Pascual M., Cardona L., Marco A., Bellido J.J., Castillo J.J., Tomás J., Raga J.A., Sanfelix M., Fernandez G., Aguilar A. 2011. Living Together but Remaining Apart: Atlantic and Mediterranean Loggerhead Sea Turtles (Caretta caretta) in Shared Feeding Grounds. J. Hered. 102: 666-677., Saied et al. 2012Saied A., Maffucci F., Hochscheid S., Dryag S., Swayeb B., Borra M., Ouerghi A., Procaccini G., Bentivegna F. 2012. Loggerhead turtles nesting in Libya: an important management unit for the Mediterranean stock. Mar. Ecol. Prog. Ser. 450: 207-224.).

These results have implications for the conservation of the species as there are large differences in abundance and conservation status among Mediterranean nesting aggregations. While the Greek nesting beaches host the largest aggregations, populations such as those found on the Levantine Mediterranean shores have extremely low numbers of nesting females (Casale and Margaritoulis 2010Casale P., Margaritoulis D. 2010. Sea turtles in the Mediterranean: distribution, threats and conservation priorities. IUCN/SSC Marine Turtle Specialist Group, Gland, Switzerland.). The structuring found among Mediterranean nesting populations (Clusa et al. 2013Clusa M., Carreras C., Pascual M., Demetropoulos A., Margaritoulis D., Rees A.F., Hamza A.A., Khalil M., Aureggi M., Levy Y., Turkozan O., Marco A., Aguilar A., Cardona L. 2013. Mitochondrial DNA reveals Pleistocenic colonisation of the Mediterranean by loggerhead turtles (Caretta caretta). J. Exp. Mar. Biol. Ecol. 439: 15-24., present study) suggests that the recolonization of other nesting beaches from the nesting females from the abundant populations of Greece in case of local extinctions would be difficult. However, the mtDNA fragment analysed in these studies is maternally inherited, so the contribution of males to gene flow among western Greece and the other Mediterranean populations is not considered. This issue remains to be tested using nuclear markers, although previous studies suggested that some male-mediated gene flow may exist within the Mediterranean (Carreras et al. 2007Carreras C., Pascual M., Cardona L., Aguilar A., Margaritoulis D., Rees A.F., Turkozan O., Levy Y., Gasith A., Aureggi M., Khalil M. 2007. The genetic structure of the loggerhead sea turtle (Caretta caretta) in the Mediterranean as revealed by nuclear and mitochondrial DNA and its conservation implications. Conserv. Genet. 8: 761-775., Yilmaz et al. 2011Yilmaz C., Turkozan O., Bardakci F. 2011. Genetic structure of loggerhead turtle (Caretta caretta) populations in Turkey. Biochem. Syst. Ecol. 39: 266-276.).

Knowledge of the genetic structuring of the Mediterranean nesting beaches has been improving since the first studies (Bowen et al. 1993Bowen B.W., Avise J.C., Richardson J.I., Meylan A., Margaritoulis D., Hopkins-Murphy S.R. 1993. Population structure of loggerhead turtles (Caretta caretta) in the Northwestern Atlantic Ocean and Mediterranean Sea. Conserv. Biol. 7: 834-844., Laurent et al. 1993Laurent L., Lescure J., Excoffier L., Bowen B.W., Domingo M., Hadjichristophorou M., Kornaraky L., Trabucht G. 1993. Genetic studies of relationships between Mediterranean and Atlantic populations of loggerhead turtle Caretta caretta with a mitochondrial marker. Comptes Rendus de l’Académie des Sciences de la Vie. Sciences de la Vie, Paris 316: 1233-1239. ), through the use of better markers or better sample sets. The present study aimed to fill one of the remaining gaps by describing one of the largest nesting beaches in the area, but there is still significant work to do. As an example, Libya is thought to host a significant portion of the Mediterranean nesting turtles and possibly has some internal genetic structuring (Saied et al. 2012Saied A., Maffucci F., Hochscheid S., Dryag S., Swayeb B., Borra M., Ouerghi A., Procaccini G., Bentivegna F. 2012. Loggerhead turtles nesting in Libya: an important management unit for the Mediterranean stock. Mar. Ecol. Prog. Ser. 450: 207-224.). A better sample size for Misurata, or samples from other unsampled Libyan nesting beaches, are needed for a full understanding of the regional structuring.

ACKNOWLEDGEMENTSTop

We wish to thank Brian Ground and the ARCHELON volunteers in Greece who collected the samples. The authors wish to acknowledge use of the Maptool program in Figure 1 of this paper. Maptool is a product of SEATURTLE.ORG (information is available at www.seaturtle.org). C. Carreras is supported by the Beatriu de Pinós programme of the Departament d’Universitats, Recerca i Societat de la Informació de la Generalitat de Catalunya. The manuscript was improved by the input of two anonymous reviewers.

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