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...

No abstract

No abstract

SUMMARYTunas (family Scombridae) and sharks in the family Lamnidae are highly convergent for features commonly related to efficient and high-performance(i.e. sustained, aerobic) swimming. High-performance swimming by fishes requires adaptations augmenting the delivery, transfer and utilization of O2 by the red myotomal muscle (RM), which powers continuous swimming. Tuna swimming performance is enhanced by a unique anterior and centrally positioned RM (i.e. closer to the vertebral column) and by structural features (relatively small fiber diameter, high capillary density and greater myoglobin concentration) increasing O2 flux from RM capillaries to the mitochondria. A study of the structural and biochemical features of the mako shark (Isurus oxyrinchus) RM was undertaken to enable performance-capacity comparisons of tuna and lamnid RM. Similar to tunas, mako RM is positioned centrally and more anterior in the body. Another lamnid, the salmon shark (Lamna ditropis), also has this RM distribution, as does the closely related common thresher shark (Alopias vulpinus; family Alopiidae). However, in both the leopard shark(Triakis semifasciata) and the blue shark (Prionace glauca),RM occupies the position where it is typically found in most fishes; more posterior and along the lateral edge of the body. Comparisons among sharks in this study revealed no differences in the total RM quantity (approximately 2–3% of body mass) and, irrespective of position within the body, RM scaling is isometric in all species. Sharks thus have less RM than do tunas(4–13% of body mass). Relative to published data on other shark species,mako RM appears to have a higher capillary density, a greater capillary-to-fiber ratio and a higher myoglobin concentration. However, mako RM fiber size does not differ from that reported for other shark species and the total volume of mitochondria in mako RM is similar to that reported for other sharks and for tunas. Lamnid RM properties thus suggest a higher O2 flux capacity than in other sharks; however, lamnid RM aerobic capacity appears to be less than that of tuna RM.