607 research outputs found

    Échapper à l'élévation des mers

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    Dans les Samoa américaines, des scientifi ques utilisent des SIG et des marégraphes pour mesurer l'évolution du repli de la mangrove suite à l'élévation du niveau des mers

    Escaping the rising sea

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    Researchers in American Samoa are employing GIS, satellite imagery and tide gauges to track the landward retreat of mangrove forests in response to rising sea level

    Elasmobranch captures in the Fijian pelagic longline fishery

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    Pelagic longline fisheries for relatively fecund tuna and tuna-like species can have large adverse effects on incidentally caught species with low-fecundity, including elasmobranchs. Analyses of observer programme data from the Fiji longline fishery from 2011 to 2014 were conducted to characterize the shark and ray catch composition and identify factors that significantly explained standardized catch rates. Catch data were fitted to generalized linear models to identify potentially significant explanatory variables. With a nominal catch rate of 0.610 elasmobranchs per 1000 hooks, a total of 27 species of elasmobranchs were captured, 48% of which are categorized as Threatened under the IUCN Red List. Sharks and rays made up 2.4% and 1.4%, respectively, of total fish catch. Blue sharks and pelagic stingrays accounted for 51% and 99% of caught sharks and rays, respectively. There was near elimination of ‘shark lines’, branchlines set at or near the sea surface via attachment directly to floats, after 2011. Of caught elasmobranchs, 35% were finned, 11% had the entire carcass retained, and the remainder was released alive or discarded dead. Finning of elasmobranchs listed in CITES Appendix II was not observed in 2014. There were significantly higher standardized shark and ray catch rates on narrower J-shaped hooks than on wider circle hooks. Based on findings from previous studies on single factor effects of hook width and shape, the smaller minimum width of the J-shaped hooks may have caused the higher shark and ray catch rates. For sharks, the effect of hook width may have exceeded the effect of hook shape, where small increases in shark catch rates have been observed on circle vs J-shaped hooks. Shark and ray standardized catch rates were lowest in the latter half of the year. Focusing effort during the second half of the year could reduce elasmobranch catch rates

    Seabird Bycatch in Pelagic Longline Fisheries Is Grossly Underestimated when Using Only Haul Data

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    Hundreds of thousands of seabirds are killed each year as bycatch in longline fisheries. Seabirds are predominantly caught during line setting but bycatch is generally recorded during line hauling, many hours after birds are caught. Bird loss during this interval may lead to inaccurate bycatch information. In this 15 year study, seabird bycatch was recorded during both line setting and line hauling from four fishing regions: Indian Ocean, Southern Ocean, Coral Sea and central Pacific Ocean. Over 43,000 albatrosses, petrels and skuas representing over 25 species were counted during line setting of which almost 6,000 seabirds attempted to take the bait. Bait-taking interactions were placed into one of four categories. (i) The majority (57%) of bait-taking attempts were “unsuccessful” involving seabirds that did not take the bait nor get caught or hooked. (ii) One-third of attempts were “successful” with seabirds removing the bait while not getting caught. (iii) One-hundred and seventy-six seabirds (3% of attempts) were observed being “caught” during line setting, with three albatross species – Laysan (Phoebastria immutabilis), black-footed (P. nigripes) and black-browed (Thalassarche melanophrys)– dominating this category. However, of these, only 85 (48%) seabird carcasses were retrieved during line hauling. Most caught seabirds were hooked through the bill. (iv) The remainder of seabird-bait interactions (7%) was not clearly observed, but likely involved more “caught” seabirds. Bait taking attempts and percentage outcome (e.g. successful, caught) varied between seabird species and was not always related to species abundance around fishing vessels. Using only haul data to calculate seabird bycatch grossly underestimates actual bycatch levels, with the level of seabird bycatch from pelagic longline fishing possibly double what was previously thought

    Ever Green: An Enduring System of Parks and Greenways in Detroit

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    http://deepblue.lib.umich.edu/bitstream/2027.42/110956/1/ever_green.pd

    Instrumental variable approaches to identifying the causal effect of educational attainment on dementia risk

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    PURPOSE: Education is an established correlate of cognitive status in older adulthood, but whether expanding educational opportunities would improve cognitive functioning remains unclear given limitations of prior studies for causal inference. Therefore, we conducted instrumental variable (IV) analyses of the association between education and dementia risk, using for the first time in this area, genetic variants as instruments as well as state-level school policies. METHODS: IV analyses in the Health and Retirement Study cohort (1998-2010) used two sets of instruments: (1) a genetic risk score constructed from three single-nucleotide polymorphisms (SNPs; n = 7981); and (2) compulsory schooling laws (CSLs) and state school characteristics (term length, student teacher ratios, and expenditures; n = 10,955). RESULTS: Using the genetic risk score as an IV, there was a 1.1% reduction in dementia risk per year of schooling (95% confidence interval, -2.4 to 0.02). Leveraging compulsory schooling laws and state school characteristics as IVs, there was a substantially larger protective effect (-9.5%; 95% confidence interval, -14.8 to -4.2). Analyses evaluating the plausibility of the IV assumptions indicated estimates derived from analyses relying on CSLs provide the best estimates of the causal effect of education. CONCLUSIONS: IV analyses suggest education is protective against risk of dementia in older adulthood

    Electronic monitoring for improved accountability in western Pacific tuna longline fisheries

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    The collection of accurate fisheries catch data is critical to ensuring sustainable management of tuna fisheries, mitigating their environmental impacts and for managing transboundary fish stocks. These challenges are exemplified by the western Pacific tuna longline fishery, who's management includes >26 nations, but is informed by critically low coverage of fishing activities by scientific observers. The gap in observer data could be filled by electronic monitoring (EM), but there are few trials that span multiple nations. A large-scale trial of EM systems on tuna longliners based in Palau, Federated States of Micronesia and the Republic of the Marshall Islands, is reported on. Comparisons are made of catch rates of market and bycatch species in corresponding EM, logbook and human observer data. Retained species were under-reported in logbooks by up to three times and discards of many species were not reported in logbooks. Discards identified in the EM data included threatened species such as marine turtles. Catch rate estimates from EM data were comparable to those estimated by human observers. EM data recorded a higher species diversity of catches than logbook data. Analysis of the EM data indicated clusters of bycatch that were associated with specific fishing practices. These results suggest further expansion of EM could inform improved management of both target and bycatch species. Ultimately greater coverage of EM data could contribute to reconciling debates in international stock allocation schemes and support actions to reduce the impacts of the fishery on threatened bycatch species

    The Solar Benchmark: Rotational Modulation of the Sun Reconstructed from Archival Sunspot Records

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    We use archival daily spot coverage measurements from Howard et al. (1984) to study the rotational modulation of the Sun as though it were a distant star. A quasi-periodic Gaussian process measures the solar rotation period Prot=26.3±0.1P_\mathrm{rot} = 26.3 \pm 0.1 days, and activity cycle period Pcyc=10.7±0.3P_\mathrm{cyc} = 10.7 \pm 0.3 years. We attempt to search for evidence of differential rotation in variations of the apparent rotation period throughout the activity cycle and do not detect a clear signal of differential rotation, consistent with the null results of the hare-and-hounds exercise of Aigrain et al. (2015). The full reconstructed solar light curve is available online.Comment: Accepted for publication in MNRA
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