2016
DOI: 10.1016/j.pocean.2016.01.006
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The influence of oceanographic features on the foraging behavior of the olive ridley sea turtle Lepidochelys olivacea along the Guiana coast

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Cited by 36 publications
(38 citation statements)
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“…The average size of our migrant turtles was larger than those found by Meylan, Meylan, and Gray () (mean CCL in Martinique: 85.9 cm vs. 81.9 cm), who performed a series of laparoscopies on juvenile green turtles in Panama to determine the minimum size at sexual maturity. Although the turtles tracked from Martinique waters were smaller (CCL range: 78.5–93 cm) than the reproductive females observed in French Guiana (CCL range: 103–133 cm, Chambault, de Thoisy, Kelle, et al, ), Costa Rica (CCL range: 95.5–110.9 cm, Troëng, Evans, Harrison, & Lagueux, ), Ascension Island (CCL range: 100–130 cm, Hays, Broderick, Glen, & Godley, ), and Guinea‐Bissau (CCL range: 92–103 cm, Godley, Almeida, et al, ; Godley, Lima, et al, ), this suggests that our migrant individuals are close to reach sexual maturity. These turtles might therefore initiate their migration, either to discover new developmental habitats (Carr, Carr, & Meylan, ) or to directly reach adult habitats (foraging grounds or breeding sites).…”
Section: Discussionmentioning
confidence: 89%
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“…The average size of our migrant turtles was larger than those found by Meylan, Meylan, and Gray () (mean CCL in Martinique: 85.9 cm vs. 81.9 cm), who performed a series of laparoscopies on juvenile green turtles in Panama to determine the minimum size at sexual maturity. Although the turtles tracked from Martinique waters were smaller (CCL range: 78.5–93 cm) than the reproductive females observed in French Guiana (CCL range: 103–133 cm, Chambault, de Thoisy, Kelle, et al, ), Costa Rica (CCL range: 95.5–110.9 cm, Troëng, Evans, Harrison, & Lagueux, ), Ascension Island (CCL range: 100–130 cm, Hays, Broderick, Glen, & Godley, ), and Guinea‐Bissau (CCL range: 92–103 cm, Godley, Almeida, et al, ; Godley, Lima, et al, ), this suggests that our migrant individuals are close to reach sexual maturity. These turtles might therefore initiate their migration, either to discover new developmental habitats (Carr, Carr, & Meylan, ) or to directly reach adult habitats (foraging grounds or breeding sites).…”
Section: Discussionmentioning
confidence: 89%
“…That is the reason why many species perform long‐distance migrations, exploiting distinct habitats during their life cycle. In the marine realm, such long migrations have been reported in seabirds (e.g., Egevang et al, ; Storr, ), cetaceans (e.g., Fossette et al, ; Garrigue et al, ; Rasmussen et al, ), pinnipeds (e.g., Hindell et al, ; Robinson et al, ), large pelagic fishes (e.g., Block et al, ; Potter, Galuardi, & Howell, ; Skomal et al, ), and sea turtles (e.g., Chambault et al, ; Chambault, de Thoisy, Heerah, et al, ; Chambault et al, ; Polovina et al, ).…”
Section: Introductionmentioning
confidence: 93%
“…Therefore, integrating ABI can complement ocean observing platforms such as Argo floats, gliders and other autonomous vehicles to provide unique and cost-effective data from poorly sampled ocean regions (Block et al, 2016;Bograd, Block, Costa, & Godley, 2010;Fedak, 2004;Harcourt et al, 2019;Hays et al, 2016;Hussey et al, 2015;Roemmich et al, 2010;Roquet et al, 2014). For instance, ABI in the marine environment have been deployed on pinnipeds (Bailleul et al, 2015;Roquet et al, 2014), cetaceans (Laidre et al, 2010), marine turtles (Chambault et al, 2015(Chambault et al, , 2016McMahon et al, 2005;McMahon & Hays, 2006;Patel et al, 2018), sharks (Coffey & Holland, 2015;Payne et al, 2018), fish (Block, Costa, Boehlert, & Kochevar, 2002), flying seabirds (Wilson et al, 2002;Wilson & Vandenabeele, 2012), penguins (Charrassin, Park, Maho, & Bost, 2002;Sala, Pisoni, & Quintana, 2017) and sirenians (Hagihara et al, 2018). Animals can travel to regions that are relatively inaccessible to other ocean observing technologies.…”
Section: Introductionmentioning
confidence: 99%
“…Not all olive ridley populations, however, are oceanic nomads; some groups have been observed to habitually occupy neritic waters near nesting sites, as observed in North West Australia (McMahon et al, 2007;Whiting et al, 2007), French Guiana (Plot et al, 2015), and Oman (Rees et al, 2012). This behavior may be explained by nearby food resource abundance, favorable temperatures, or other oceanic conditions (Plot et al, 2015;Chambault et al, 2016Chambault et al, , 2017 but nevertheless demonstrates significant behavioral plasticity for the species throughout their global range.…”
Section: Introductionmentioning
confidence: 99%
“…Through their nomadic migrations these turtles can encounter different local environmental conditions, which can determine the travel direction, traveling speed, diving behavior and residence time (Chambault et al, 2016(Chambault et al, , 2017(Chambault et al, , 2019. Mesoscale eddies, which drive ocean productivity in the open ocean, transport heat, salts and nutrients (Revelles et al, 2007), are known to aggregate different sea turtle species, both in cold-core cyclonic eddies, and in warm-core anticyclonic eddies (Polovina et al, 2006;Mansfield et al, 2014;Chambault et al, 2016Chambault et al, , 2019.…”
Section: Introductionmentioning
confidence: 99%