White sharks, Carcharodon carcharias, are often described as elusive, with little information available due to the logistical difficulties of studying large marine predators that make long-distance migrations across ocean basins. Increased understanding of aggregation patterns, combined with recent advances in technology have, however,
The number of shark-human interactions and shark bites per capita has been increasing since the 1980s, leading to a rise in measures developed to mitigate the risk of shark bites. Yet many of the products commercially available for personal protection have not been scientifically tested, potentially providing an exaggerated sense of security to the people using them. We tested five personal shark deterrents developed for surfers (Shark Shield Pty Ltd [Ocean Guardian] Freedom+ Surf, Rpela, SharkBanz bracelet, SharkBanz surf leash, and Chillax Wax) by comparing the percentage of baits taken, distance to the bait, number of passes, and whether a shark reaction could be observed. We did a total of 297 successful trials at the Neptune Islands Group Marine Park in South Australia, during which 44 different white sharks (Carcharodon carcharias) interacted with the bait, making a total of 1413 passes. The effectiveness of the deterrents was variable, with the Freedom+ Surf affecting shark behaviour the most and reducing the percentage of bait taken from 96% (relative to the control board) to 40%. The mean distance of sharks to the board increased from 1.6 ± 0.1 m (control board) to 2.6 ± 0.1 m when the Freedom Surf+ was active. The other deterrents had limited or no measureable effect on white shark behavour. Based on our power analyses, the smallest effect size that could be reliably detected was ∼15%, which for the first time provides information about the effect size that a deterrent study like ours can reliably detect. Our study shows that deterrents based on similar principles—overwhelming a shark’s electroreceptors (the ampullae of Lorenzini) with electrical pulses—differ in their efficacy, reinforcing the need to test each product independently. Our results will allow private and government agencies and the public to make informed decisions about the use and suitability of these five products.
The use of fatty acid (FA) tracers is a growing tool in trophic ecology, yet FA profiles are driven by a number of abiotic and biotic parameters, making interpretation and appropriate use confusing for ecologists.
We undertook a global analysis, compiling FA profiles of 106 chondrichthyan (shark, ray and chimaera) populations, as a model to test the utility of FA profiles to partition a priori trophic guilds, phylogeny, water temperature and habitats. Individual FAs characterizing these four factors were identified, promoting the use of these FAs as ecological tracers across taxa.
Habitat type was linked to five FAs: 16:0, 18:0 and biologically essential 22:6ω3 (indicative of the deep sea), 20:5ω3 (non‐complex demersal and deep‐sea demersal) and 20:4ω6 (reef and brackish water). Temperature was a key driver of four FAs (22:5ω6, 22:4ω6, 20:1ω9 and 20:5ω3), while trophic guild and phylogeny were important drivers of two pairs of FA tracers (18:0 and 20:5ω3; 20:1ω9 and 18:1ω9, respectively).
This analysis provides a novel understanding of the biological and ecological information that can be inferred from FA profiles and further validates the use of FAs as tracers to investigate the trophic ecology of chondrichthyans.
Future research should prioritize ex situ studies to further disentangle the influence of factors across taxa and tissue types, quantify biomodification, enabling the use of quantitative methods for diet determination and further develop ‘FATscapes’ to elucidate fine‐scale trophic geography and climate variability. Additionally, the creation of a taxonomically inclusive FA data repository will enable further meta‐analyses.
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