6 research outputs found

    Population productivity of shovelnose rays: inferring the potential for recovery

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    Copyright: This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. There is recent evidence of widespread declines of shovelnose ray populations (Order Rhinopristiformes) in heavily fished regions. These declines, which are likely driven by high demand for their fins in Asian markets, raises concern about their risk of over-exploitation and extinction. Using life-history theory and incorporating uncertainty into a modified Euler-Lotka model, the maximum intrinsic rates of population increase (rmax) were estimated for nine species from four families of Rhinopristiformes, using four different natural mortality estimators. Estimates of mean rmax, across the different natural mortality methods, varied from 0.03 to 0.59 year-1 among the nine species, but generally increased with increasing maximum size. Comparing these estimates to rmax values for other species of chondrichthyans, the species Rhynchobatus australiae, Glaucostegus typus, and Glaucostegus cemiculus were relatively productive, while most species from Rhinobatidae and Trygonorrhinidae had relatively low rmax values. If the demand for their high-value products can be addressed then population recovery for some species is likely possible, but will vary depending on the species

    Age, growth and maturity of oceanic whitetip shark (Carcharhinus longimanus) from Papua New Guinea

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    Oceanic whitetip sharks (Carcharhinus longimanus) in the Western Central Pacific have been overfished and require improved assessment and management to enable planning of recovery actions. Samples from 103 individuals (70 males and 33 females; 76.0-240- and 128-235-cm total length (TL) respectively) were used to estimate age, growth and maturity parameters from sharks retained by longline fisheries in Papua New Guinea. Back-calculation was used because of the low number of juveniles and a multimodel framework with Akaike's information criterion corrected for small sample size (AIC(c)) estimated growth parameters. The von Bertalanffy growth model provided the best fitting growth model for both sexes. Parameter estimates for males were: asymptotic length (L-infinity) = 315.6 cm TL; growth coefficient (k) = 0.059 year(-1); and length at birth (L-0) = 75.1 cm TL. For females, the parameter estimates were: L-infinity = 316.7 cm TL; k = 0.057 year(-1); and L-0 = 74.7 cm TL. Maximum age was estimated to be 18 years for males and 17 years for females, with a calculated longevity of 24.6 and 24.9 years respectively. Males matured at 10.0 years and 193 cm TL, whereas females matured at 15.8 years and 224 cm TL. C. longimanus is a slow-growing, late-maturity species, with regional variation in life history parameters, highlighting increased vulnerability to fishing pressure in this region

    Age and growth of tiger shark (Galeocerdo cuvier) from Western Australia

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    The tiger shark (Galeocerdo cuvier) is believed to be a fast-growing shark that has shown regional variation in growth. Vertebrae samples were taken from 124 tiger sharks (60 females, 38 males, 26 of unknown sex) caught in Western Australia (WA) from 1994 to 1998. Samples were aged using standard vertebral ageing techniques, and the data were used to create length-at-age curves. Dahl-Lee back-calculation was used because of the low number of small juveniles (<140-cm fork length, FL) captured. Males (n = 38) were found to have an age range of 3-21 years and a length range of 145-306 cm FL; females (n = 60) had an age range of 2-31 years and a length range of 118-361 cm FL. A Bayesian multi-model approach to growth-curve fitting was used, and the von Bertalanffy model provided the best fit to back-calculated data on the basis of deviance information criterion (DIC). Parameter estimates for the combined-sex back-calculated data were as follows: Asymptotic length (L∞) = 372 cm FL; growth-completion coefficient (k) = 0.067 year-1; and length-at-birth (L0) = 65.8 cm FL. Growth of WA tiger sharks was slower than that of tiger sharks from most other regions, but similar to that observed on the eastern coast of Australia

    Untangling the Indonesian tangle net fishery: Describing a data-poor fishery targeting large, threatened rays (Superorder Batoidea)

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    1.Shark-like rays (Order Rhinopristiformes) are among the most threatened families of marine fish, yet little is known about their populations. These rays are normally taken as opportunistic catch in fisheries targeting other species and are thus poorly reported. One exception is the Indonesian tangle net fishery, which targets shark-like rays. 2.Market surveys of Muara Angke landing site in Jakarta, north-western Java were conducted between 2001 and 2005, and the landed catch from the tangle net fishery was recorded (the Muara Angke landing site includes landings from more than one fishery). 3.In total, 1,559 elasmobranchs (sharks and rays) were recorded, comprising 24 species of rays and nine species of sharks. The most abundant species landed were the pink whipray Pateobatis fai and the bottlenose wedgefish Rhynchobatus australiae, the latter being the main target species. 4.Catch composition varied based on differences in species catchability and may also be indicative of localized declines. The fishery was highly selective for larger sized individuals, while smaller size classes of many ray species, including the target species, were also caught in other Indonesian fisheries, resulting in fishing pressure across all age classes. 5.The decline of tangle net vessels in the fishery and the potential shift in catch composition in the Indonesian tangle net fishery increase concerns about the status of shark-like rays and stingrays in Indonesia

    Can multi-species shark longline fisheries be managed sustainably using size limits? Theoretically, yes. Realistically, no

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    Size limits are a common fisheries management strategy that are applied to many fisheries and species. Most size limits use a minimum legal size to protect adult fish as per the ‘reproduce at least once’ paradigm, where stock collapse becomes impossible if every adult can produce one spawner prior to harvest. These approaches can be useful in fisheries where determining catch is difficult and therefore catch limits can be ineffective and potentially cause stock decline. Shark longline fisheries can be complicated to manage due to a deficiency of species-level reporting. Catch limits are therefore difficult to determine, creating a need for other management measures. Here, three different size-based management approaches were tested using the shark longline fishery from Papua New Guinea as a case study. These approaches included minimum size, maximum size and harvest slot approaches. Age-structured Leslie matrix models revealed a broad range of productivities for 12 commonly caught species, ranging from low population growth rates of 1% per year for pelagic thresher sharks Alopias pelagicus to >33% per year for blue sharks Prionace glauca. Therefore, different harvest strategies were required for each species to be fished sustainably. However, management could be applied by grouping similar and easily distinguishable groups of species together. Synthesis and applications. The most pragmatic harvest strategy for all shark species included in this study was to limit harvest to mature individuals using minimum legal sizes. This provided sufficient resilience for all species to tolerate higher levels of fishing mortality than the Papua New Guinea (PNG) longline fishery could impose. Legal minimum lengths were derived from the largest length-at-maturity within each species group. However, while this produced a sustainable harvest strategy, issues with selectivity, post-release mortality, interactions with other fisheries, economic viability and illegal, underreported and unregulated fishing were challenges to restricting fishing to the correct size classes and overall management efficacy. Therefore, while theoretically viable harvest strategies were outlined, it is apparent that size limits would not ensure that these shark species are fished sustainably. Therefore, the PNG longline fishery cannot operate sustainably if it were to reopen using size limits as its sole management strategy

    Widespread diversity deficits of coral reef sharks and rays

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    A global survey of coral reefs reveals that overfishing is driving resident shark species toward extinction, causing diversity deficits in reef elasmobranch (shark and ray) assemblages. Our species-level analysis revealed global declines of 60 to 73% for five common resident reef shark species and that individual shark species were not detected at 34 to 47% of surveyed reefs. As reefs become more shark-depleted, rays begin to dominate assemblages. Shark-dominated assemblages persist in wealthy nations with strong governance and in highly protected areas, whereas poverty, weak governance, and a lack of shark management are associated with depauperate assemblages mainly composed of rays. Without action to address these diversity deficits, loss of ecological function and ecosystem services will increasingly affect human communities
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