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World Status, Exploitation and Trade - WIDECAST

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INTRODUCTIONMigration <strong>and</strong> philopatry: malesOverall, whilst there is very little direct information on long distancereproductive movements of adult male sea turtles, the few data that areavailable are consistent with the pattern demonstrated for adult females.Virtually all tagging programmes have exclusively involved tagging femaleson the nesting beach; very few males have ever been tagged <strong>and</strong>, in thegeneral absence of suitable tag-return data, there is very little evidencefor philopatry in males. Males, of course, contribute half of the totalgenetic constitution of the population. It may well be the case that malesfeed <strong>and</strong> migrate with the females from each population, but perhaps someproportion of them disperse widely <strong>and</strong> subsequently join any convenientfemale aggregation.The best evidence available on male movements in Chelonia mydas relates tothe apparently isolated C. mydas population in Hawaii (Dizon <strong>and</strong> Balazs,1982). Two males, tagged in 1975 <strong>and</strong> 1970, were recorded to remigrate tothe same nest area in later years, in 1976 <strong>and</strong> 1977, <strong>and</strong> in 1979,respectively (radio telemetry indicated that both males <strong>and</strong> females remainclosely associated with the nesting beach area during the nesting season).Overall, during the ten-year period up to 1982, 294 turtles tagged at theHawaii nesting ground have been re-sighted, <strong>and</strong> this includes 87 males(Balazs, 1983). Seven of these males have been shown to make long distancemigrations between feeding grounds <strong>and</strong> the nesting area (or vice versa), <strong>and</strong>one of the seven has been recorded to make the return journey from feedinggrounds to the nesting area <strong>and</strong> back (Balazs, 1983). Three of 575 malestagged in the Galapagos, presumably while breeding, were subsequentlyrecaptured; one in Costa Rica <strong>and</strong> two in Peru (Green, 1984a). Similarly,two males tagged on Scilly in French Polynesia were subsequently recapturedin Fiji; females from this population have also been recaptured at othersites in western Oceania (Anon, 1979).Hawksbill migrationAlthough little concerted tagging of Hawksbills has been undertaken, <strong>and</strong> isdifficult in the absence of dense nesting aggregations, there is littleevidence as yet to counter the prevailing notion that the species tends tobe a mainly sedentary coral reef dweller; equally, there is little evidencesubstantiating the idea. A few examples of apparently purposefullong-distance migration are known (Parmenter, 1983). These include:movement between the Solomon Isl<strong>and</strong>s <strong>and</strong> Papua New Guinea, the TorresStraits <strong>and</strong> the Solomons, Sabah <strong>and</strong> the central Philippines, Tortuguero(Costa Rica) <strong>and</strong> Nicaragua. It may well be that the small number ofreported long distance movements is a simple function of the small number ofHawksbills that have been tagged <strong>and</strong> recaptured, <strong>and</strong> it is possible thatindividuals move long distances between feeding <strong>and</strong> nesting areas, <strong>and</strong> amongdifferent feeding areas, more commonly than observations indicate.Maturation periodCaptive-reared Green Turtle females (at Cayman Turtle Farm) become sexuallymature at a minimum of 8 or 9 years; the mean age of maturation at CTF isprobably greater than this (Wood <strong>and</strong> Wood, 1980), perhaps 10 or 11 years ormore. Until quite recently it had widely been assumed that maturation inthe wild occurred after a similar period (sources cited by Hirth, 1971).17

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