56 research outputs found

    High Post-Capture Survival for Sharks, Rays and Chimaeras Discarded in the Main Shark Fishery of Australia?

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    Most sharks, rays and chimaeras (chondrichthyans) taken in commercial fisheries are discarded (i.e. returned to the ocean either dead or alive). Quantifying the post-capture survival (PCS) of discarded species is therefore essential for the improved management and conservation of this group. For all chondrichthyans taken in the main shark fishery of Australia, we quantified the immediate PCS of individuals reaching the deck of commercial shark gillnet fishing vessels and applied a risk-based method to semi-quantitatively determine delayed and total PCS. Estimates of immediate, delayed and total PCS were consistent, being very high for the most commonly discarded species (Port Jackson shark, Australian swellshark, and spikey dogfish) and low for the most important commercial species (gummy and school sharks). Increasing gillnet soak time or water temperature significantly decreased PCS. Chondrichthyans with bottom-dwelling habits had the highest PCS whereas those with pelagic habits had the lowest PCS. The risk-based approach can be easily implemented as a standard practice of on-board observing programs, providing a convenient first-step assessment of the PCS of all species taken in commercial fisheries

    Diving into the vertical dimension of elasmobranch movement ecology

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    This is the final version. Available on open access from the American Association for the Advancement of Science via the DOI in this recordData and materials availability: Processed data and code used in the analysis are accessible from the Zenodo Repository: 10.5281/zenodo.6885455Knowledge of the three-dimensional movement patterns of elasmobranchs is vital to understand their ecological roles and exposure to anthropogenic pressures. To date, comparative studies among species at global scales have mostly focused on horizontal movements. Our study addresses the knowledge gap of vertical movements by compiling the first global synthesis of vertical habitat use by elasmobranchs from data obtained by deployment of 989 biotelemetry tags on 38 elasmobranch species. Elasmobranchs displayed high intra- and interspecific variability in vertical movement patterns. Substantial vertical overlap was observed for many epipelagic elasmobranchs, indicating an increased likelihood to display spatial overlap, biologically interact, and share similar risk to anthropogenic threats that vary on a vertical gradient. We highlight the critical next steps toward incorporating vertical movement into global management and monitoring strategies for elasmobranchs, emphasizing the need to address geographic and taxonomic biases in deployments and to concurrently consider both horizontal and vertical movements.Bertarelli FoundationResearch EnglandMoore FoundationPackard FoundationInstituto Politecnico NacionalDarwin InitiativeGeorgia AquariumRolex Awards for EnterpriseWhitley Fund for Natur

    Relative eye size in elasmobranchs

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    Variation in relative eye size was investigated in a sample of 46 species of elasmobranch, 32 species of sharks and 14 species of batoids (skates and rays). To get a measure of eye size relative to body size, eye axial diameter was scaled with body mass using least-squares linear regression, using both raw species data, where species are treated as independent data points, and phylogenetically independent contrasts. Residual values calculated for each species, using the regression equations describing these scaling relationships, were then used as a measure of relative eye size. Relative and absolute eye size varies considerably in elasmobranchs, although sharks have significantly relatively larger eyes than batoids. The sharks with the relatively largest eyes are oceanic species; either pelagic sharks that move between the epipelagic (0 -200 m) and 'upper' mesopelagic (200-600 m) zones, or benthic and benthopelagic species that live in the mesopelagic (200-1,000 m) and, to a lesser extent, bathypelagic (1,000-4,000 m) zones. The elasmobranchs with the relatively smallest eyes tend to be coastal, often benthic, batoids and sharks. Active benthopelagic and pelagic species, which prey on active, mobile prey also have relatively larger eyes than more sluggish, benthic elasmobranchs that feed on more sedentary prey such as benthic invertebrates. A significant positive correlation was found between absolute eye size and relative eye size, but some very large sharks, such as Carcharodon carcharias have absolutely large eyes, but have relatively small eyes in relation to body mass. Copyright © 2007 S. Karger AG, Base

    A web-based archive for topographic maps of retinal cell distribution in vertebrates

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    Clinical and Experimental Optometry, in conjunction with Optometrists Association Australia and Professor Shaun P Collin of the University of Queensland, announce the launch of a web-based archive of previously published topographic maps of retinal cell distribution in vertebrates. At present, the archive boasts more than 770 different maps of the distribution of retinal neurons (for example, photoreceptors, bipolar cells, amacrine cells, horizontal cells and ganglion cells) in nearly 200 species within all vertebrate classes (Cephalospidomorpha, Actinopterygii, Sarcopterygii, Amphibia, Reptilia, Aves and Mammalia). The distribution of retinal neurons has been studied for more than 100 years and has become a powerful means of predicting the spatial resolving power of the eye and the retinal regions containing specialisations, such as areae centrales, horizontal streaks and foveae, where increased densities of neurons define the way in which a species visually samples its environment. The location of these retinal specialisations thereby identifies the part(s) of the visual field of critical importance for localising food and mates and for predator surveillance. The distribution of sampling elements even reflects the symmetry of a species' ecological habitat. The archive is a unique collection of most of the currently available retinal maps, which also presents relevant information, where known, about eye size, retinal cell density, retinal orientation, cell number, spatial resolving power and the type of specialisation, in addition to basic physical parameters of each species (body size, weight, sex and developmental stage). The archive is accessible at http://www.optometrists.asn.au/ceo/retinalsearch and will be updated regularly. The powerful database is interactive and freely available, providing the opportunity to upload both published and unpublished topographic maps. Following a review process, previously unpublished maps will be 'published' and available online worldwide. It is hoped that this comprehensive new resource will provide not only an up-to-date method of accessing maps of the distribution of retinal neurons in individual species but also allow broader evolutionary comparisons of the visual capabilities, ecology, development and the type(s) of retinal specialisations found in vertebrates
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