506 research outputs found

    How Much Longer Will it Take? A Ten-year Review of the Implementation of United Nations General Assembly Resolutions 61/105, 64/72 and 66/68 on the Management of Bottom Fisheries in Areas Beyond National Jurisdiction

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    The United Nations General Assembly (UNGA) in 2002 adopted the first in a series of resolutions regarding the conservation of biodiversity in the deep sea. Prompted by seriousconcerns raised by scientists, non-governmental organizations (NGOs) and numerous States,these resolutions progressively committed States to act both individually and through regional fishery management organizations (RFMOs) to either manage bottom fisheries in areas beyond national jurisdiction to prevent significant adverse impacts on deep-sea species, ecosystems and biodiversity or else prohibit bottom fishing from taking place.Ten years have passed since the adoption of resolution 61/105 in 2006, calling on States to take a set of specific actions to manage bottom fisheries in areas beyond national jurisdiction to protect vulnerable marine ecosystems (VMEs) from the adverse impacts of bottom fishing and ensure the sustainability of deep-sea fish stocks. Despite the considerable progress by some RFMOs, there remain significant gaps in the implementation of key elements and commitments in the resolutions. The Deep Sea Conservation Coalition (DSCC) has prepared this report to assist the UNGA in its review in 2016 and to address the following question: How effectively have the resolutions been implemented

    Commentary: consistency of EEG source localization and connectivity estimates

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    Bahar Moezzi and Mitchell R. Goldsworth

    Colony-specific foraging areas of lactating New Zealand fur seals

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    Copyright © 2008 Inter-Research.During 2005 and 2006, 21 lactating New Zealand fur seals Arctocephalus forsteri were tracked from 4 breeding colonies in southern Australia. The distance between colonies ranged between 46 and 207 km. In total, 101 foraging trips were recorded (2 to 19 trips ind.–1). Seals initiated foraging trips on a colony-specific bearing (Cape Gantheaume 141 ± 34°, Cape du Couedic 188 ± 12°, North Neptune Island 204 ± 12° and Liguanea Island 235 ± 19°). During autumn, seals from Cape du Couedic, North Neptune Island and Liguanea Island predominantly targeted distant oceanic waters associated with the subtropical front (STF), while seals from Cape Gantheaume targeted shelf waters associated with a seasonal coastal upwelling, the Bonney upwelling. The distance of each colony from the STF (based on the preferred colony bearing) or the Bonney upwelling in the case of Cape Gantheaume was correlated with the maximum straight-line distances travelled (Cape Gantheaume 119 ± 57 km, Cape du Couedic 433 ± 99 km, North Neptune Island 564 ± 97 km and Liguanea Island 792 ± 82 km). The organisation of colony-specific foraging grounds appears to be influenced by the proximity of colonies to predictable local upwelling features, as well as distant oceanic frontal zones. Knowledge of whether New Zealand fur seals utilise colony-specific foraging grounds may be important in predicting and identifying critical habitats and understanding whether management requirements are likely to vary between different colonies.Alastair Martin Mitri Baylis, Brad Page, Simon David Goldsworth

    Spatial separation of foraging habitats among New Zealand fur seals

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    We studied the foraging behaviour of lactating female, adult male and juvenile New Zealand (NZ) fur seals to compare and contrast their foraging strategies and assess the degree of spatial separation of their foraging habitats. Adult male fur seals are longer and heavier than lactating females, which are longer and heavier than juveniles. Trip duration was positively correlated with the distance travelled by all age/sex groups. Juveniles conducted longer trips and travelled further from the colony than males. Both juveniles and males conducted longer trips and travelled further than females, which made brief trips because they were provisioning pups. There were no seasonal differences in the behaviour of males, but females and juveniles foraged closer to the colony in summer when they were moulting and females had younger pups. Behavioural differences were recorded between lactating female, male and juvenile seals in the directional bearing from the colony, the distance travelled, the minimum size of the area that was potentially visited and the horizontal swim speed. Intra-specific foraging competition among these age/sex groups was minimal because lactating females typically used continental shelf waters and males utilised deeper waters over the shelf break, adjacent to female foraging grounds. Furthermore, juveniles used pelagic waters, up to 1000 km south of the habitats used by adults. Differences in the habitats used by females, males and juveniles were also apparent in the seafloor gradient, the SST and the surface chl a concentration, with females using regions with the highest chl a concentrations. Results from this study suggest that smaller seals cannot efficiently utilise prey in the same habitats as larger seals because smaller seals do not have the capacity to spend enough time underwater at the greater depths.Brad Page, Jane McKenzie, Michael D. Sumner, Michael Coyne, Simon D. Goldsworth

    The purpose of mess in action research: building rigour though a messy turn

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    Mess and rigour might appear to be strange bedfellows. This paper argues that the purpose of mess is to facilitate a turn towards new constructions of knowing that lead to transformation in practice (an action turn). Engaging in action research - research that can disturb both individual and communally held notions of knowledge for practice - will be messy. Investigations into the 'messy area', the interface between the known and the nearly known, between knowledge in use and tacit knowledge as yet to be useful, reveal the 'messy area' as a vital element for seeing, disrupting, analysing, learning, knowing and changing. It is the place where long-held views shaped by professional knowledge, practical judgement, experience and intuition are seen through other lenses. It is here that reframing takes place and new knowing, which has both theoretical and practical significance, arises: a 'messy turn' takes place

    Effects of an electric field on white sharks: in situ testing of an electric deterrent

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    Elasmobranchs can detect minute electromagnetic fields, <1 nV cm(-1), using their ampullae of Lorenzini. Behavioural responses to electric fields have been investigated in various species, sometimes with the aim to develop shark deterrents to improve human safety. The present study tested the effects of the Shark Shield Freedom7ℱ electric deterrent on (1) the behaviour of 18 white sharks (Carcharodon carcharias) near a static bait, and (2) the rates of attacks on a towed seal decoy. In the first experiment, 116 trials using a static bait were performed at the Neptune Islands, South Australia. The proportion of baits taken during static bait trials was not affected by the electric field. The electric field, however, increased the time it took them to consume the bait, the number of interactions per approach, and decreased the proportion of interactions within two metres of the field source. The effect of the electric field was not uniform across all sharks. In the second experiment, 189 tows using a seal decoy were conducted near Seal Island, South Africa. No breaches and only two surface interactions were observed during the tows when the electric field was activated, compared with 16 breaches and 27 surface interactions without the electric field. The present study suggests that the behavioural response of white sharks and the level of risk reduction resulting from the electric field is contextually specific, and depends on the motivational state of sharks.Charlie Huveneers, Paul J. Rogers, Jayson M. Semmens, Crystal Beckmann, Alison A. Kock, Brad Page, Simon D. Goldsworth

    Non-Equilibrium Reaction Rates in the Macroscopic Chemistry Method for DSMC Calculations

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    The Direct Simulation Monte Carlo (DSMC) method is used to simulate the flow of rarefied gases. In the Macroscopic Chemistry Method (MCM) for DSMC, chemical reaction rates calculated from local macroscopic flow properties are enforced in each cell. Unlike the standard total collision energy (TCE) chemistry model for DSMC, the new method is not restricted to an Arrhenius form of the reaction rate coefficient, nor is it restricted to a collision cross-section which yields a simple power-law viscosity. For reaction rates of interest in aerospace applications, chemically reacting collisions are generally infrequent events and, as such, local equilibrium conditions are established before a significant number of chemical reactions occur. Hence, the reaction rates which have been used in MCM have been calculated from the reaction rate data which are expected to be correct only for conditions of thermal equilibrium. Here we consider artificially high reaction rates so that the fraction of reacting collisions is not small and propose a simple method of estimating the rates of chemical reactions which can be used in the Macroscopic Chemistry Method in both equilibrium and non-equilibrium conditions. Two tests are presented: (1) The dissociation rates under conditions of thermal non-equilibrium are determined from a zero-dimensional Monte-Carlo sampling procedure which simulates ‘intra-modal’ non-equilibrium; that is, equilibrium distributions in each of the translational, rotational and vibrational modes but with different temperatures for each mode; (2) The 2-D hypersonic flow of molecular oxygen over a vertical plate at Mach 30 is calculated. In both cases the new method produces results in close agreement with those given by the standard TCE model in the same highly nonequilibrium conditions. We conclude that the general method of estimating the non-equilibrium reaction rate is a simple means by which information contained within non-equilibrium distribution functions predicted by the DSMC method can be included in the Macroscopic Chemistry Method
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