The large-scale spatial dynamics and population structure of marine top predators are poorly known. We present electronic tag and photographic identification data showing a complex suite of behavioral patterns in white sharks. These include coastal return migrations and the fastest known transoceanic return migration among swimming fauna, which provide direct evidence of a link between widely separated populations in South Africa and Australia. Transoceanic return migration involved a return to the original capture location, dives to depths of 980 meters, and the tolerance of water temperatures as low as 3.4 degrees C. These findings contradict previous ideas that female white sharks do not make transoceanic migrations, and they suggest natal homing behavior.
Effective ocean management and conservation of highly migratory species depends onresolving overlap between animal movements and distributions, and fishing effort.However, this information is lacking at a global scale. Here we show, using a big-data approach that combines satellite-tracked movements of pelagic sharks and global fishing fleets, that 24% of the mean monthly space used by sharks falls under the footprint of pelagic longline fisheries. Space-use hotspots of commercially valuable sharks and of internationally protected species had the highest overlap with longlines (up to 76% and 64%, respectively), and were also associated with significant increases in fishing effort.We conclude that pelagic sharks have limited spatial refuge from current levels of fishing effort in marine areas beyond national jurisdictions (the high seas). Our results demonstrate an urgent need for conservation and management measures at high-seas hotspots of shark space use, and highlight the potential of simultaneous satellite surveillance of megafauna and fishers as a tool for near-real-time, dynamic management.Industrialised fishing is a major source of mortality for large marine animals (marine megafauna) 1-6 . Humans have hunted megafauna in the open ocean for at least 42,000 years 7 , but international fishing fleets targeting large, epipelagic fishes did not spread into the high seas (areas beyond national jurisdiction) until the 1950s 8 . Prior to this, the high seas constituted a spatial refuge largely free from exploitation as fishing pressure was concentrated on continental shelves 3,8 . Pelagic sharks are among the widest ranging vertebrates, with some species exhibiting annual ocean-basin-scale migrations 9 , long term trans-ocean movements 10 , and/or fine-scale site fidelity to preferred shelf and open ocean areas 5,9,11 . These behaviours could cause extensive spatial overlap with different fisheries from coastal areas to the deep ocean. On average, large pelagic sharks account for 52% of all identified shark catch worldwide in target fisheries or as bycatch 12 . Regional declines in abundance of pelagic sharks have been reported 13,14 , but it is unclear whether exposure to high fishing effort extends across ocean-wide population ranges and overlaps areas in the high seas where sharks are most abundant 5,13 .Conservation of pelagic sharkswhich currently have limited high seas management 12,15,16would benefit greatly from a clearer understanding of the spatial relationships between sharks' habitats and active fishing zones. However, obtaining unbiased estimates of shark and fisher distributions is complicated by the fact that most data on pelagic sharks come from catch records and other fishery-dependent sources 4,15,16 .Here, we provide the first global estimate of the extent of space use overlap of sharks with industrial fisheries. This is based on the analysis of the movements of pelagic sharks tagged with satellite transmitters in the Atlantic, Indian and Pacific oceans, together with fishing vessel movements m...
Between June and December 2005, active and passive acoustic telemetry was used to examine fine scale movements of 13 white sharks (Carcharodon carcharias) (ten passive, three active) at Mossel Bay. A total of 24 active trackings (ranging from 2 h to 103 h in duration) were conducted. Patterns of rate of movement (ROM), swimming linearity (LI), swimming bearing, and instantaneous swimming speed (ISS) were assessed. A conversion quotient (Q) of 1.21 between ISS and ROM (10 min sample interval) was calculated suggesting ROM is a good indicator of white shark activity. The mean ROM for tracked sharks was 0.52 m·s −1 , with a greatest sustained ROM of 1.33 m·s −1 (4.8 km·h −1 ).Sharks displayed greatest LI and ROM during directional travels between the three persistent aggregation sites. The majority of the shark movement was, however, non-linear as the sharks repeat patrolled at the three aggregation sites. Two of these sites were not associated with pinniped presence, and sharks typically patrolled back and forth parallel to the shore line at a comparatively low ROM which suggested resting. The third aggregation site was adjacent to Seal Island, and despite low LI, sharks displayed a high ROM, indicating high activity levels. We propose that the high ROM is related to maximising search area when patrolling to hunt Cape fur seals (Arctocephalus p. pusillus).
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