2020
DOI: 10.1038/s41598-020-75183-6
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A biphasic navigational strategy in loggerhead sea turtles

Abstract: The homing journeys of nine loggerhead turtles translocated from their nesting beach to offshore release sites, were reconstructed through Argos and GPS telemetry while their water-related orientation was simultaneously recorded at high temporal resolution by multi-sensor data loggers featuring a three-axis magnetic sensor. All turtles managed to return to the nesting beach area, although with indirect routes encompassing an initial straight leg not precisely oriented towards home, and a successive homebound s… Show more

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Cited by 9 publications
(7 citation statements)
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“…Turtles travelling to targets on mainland coasts may simply have to make the correct decision to turn left or right when reaching the coast and then can follow the shore to their destination [ 14 , 37 ]. In a similar way, migrating birds may reorientate homewards when they reach land after a sea crossing [ 28 ] and many terrestrial animals use visual landmarks to orientate [ 38 , 39 ].…”
Section: Discussionmentioning
confidence: 99%
“…Turtles travelling to targets on mainland coasts may simply have to make the correct decision to turn left or right when reaching the coast and then can follow the shore to their destination [ 14 , 37 ]. In a similar way, migrating birds may reorientate homewards when they reach land after a sea crossing [ 28 ] and many terrestrial animals use visual landmarks to orientate [ 38 , 39 ].…”
Section: Discussionmentioning
confidence: 99%
“…Our results indicate a period of consistent, immediate offshore dispersal in white sharks after release from capture, with most individuals relocating into continental shelf waters (≥40-60 m depth, ∼10-30 km offshore) within ∼6 h and remaining there for the duration of their deployments (up to 136.2 h). Although some animals can exhibit disorientation and reduced movement rates immediately following capture (e.g., Luschi et al, 2020), rapid post-release offshore movements, similar to our observations in white sharks, have also been described across a range of marine taxa (Gunn et al, 2003;Mangel et al, 2011;Afonso and Hazin, 2014;Barnes et al, 2016), and have been interpreted to be a "flight" response associated with capture stress (Lear and Whitney, 2016). Supporting this explanation, offshore dispersal of white sharks coincided with a period of faster tailbeats (i.e., rapid movement), which gradually slowed to a more constant average rate, indicating a population-level recovery period (return to "baseline" tailbeat signature) of 9.7 h. This pattern and rate of TBC recovery is similar to that identified for common blacktip sharks (Carcharhinus limbatus, 9 h; Whitney et al, 2016), but longer than for tiger sharks (Galeocerdo cuvier, 4 h; Andrzejaczek et al, 2019a), potentially suggesting lower sensitivity to capture in tiger sharks (consistent with Gallagher et al, 2014).…”
Section: Discussionmentioning
confidence: 99%
“…Another mechanism could be the interaction of atropine and dopamine release [ 8 ]. While proteomic studies in retinal cells are ongoing, treatment with atropine in humans was accompanied by an increase of choroidal thickness and abolished choroidal thinning due to hyperopic defocus [ 71 ]. This is reminiscent of very similar observations in animal models: muscarinic acetylcholine agonists cause choroidal thinning in chickens, whereas antagonists cause thickening [ 72 ].…”
Section: Discussionmentioning
confidence: 99%