308 research outputs found

    Investigation of the Stock Structure of Atlantic Walrus (Odobenus rosmarus rosmarus) in Canada and Greenland Using Dental Pb Isotopes Derived from Local Geochemical Environments

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    The chemical composition of animal tissues such as teeth appears to reflect an individual's exposure to its geochemical environment. In this study, the lead (Pb) isotope composition of dental cementum was used to investigate the stock structure of Atlantic walrus (Odobenus rosmarus rosmarus) in the Canadian Arctic and Greenland. The 12 communities providing walrus samples for this study represent most of the Canadian and Greenlandic villages where walrus still form an important part of the traditional Inuit diet. Significant differences between locations in mean Pb isotope ratios and the limited overlap of the ranges of values indicate that each village harvested walrus herds that exploited substantially different geological/geographical habitats. This geographic segregation based on isotopic signatures suggests that most walrus stocks (i.e., the groups of walrus that interact with hunters at each community) are more localized in their range than previously thought. 208Pb/207Pb and 208Pb/204Pb were the most important stock discriminators, reflecting the influence of local geological Th/U composition (i.e., 208Pb) on Pb isotope composition in walrus teeth. 204Pb-based isotope ratios in walrus were consistently higher (more radiogenic) and more homogeneous than those in regional terrestrial bedrock, a difference probably due to selective leaching of radiogenic Pb from mineral phases into seawater and mixing during weathering and transport. Dental Pb isotope signatures may have widespread application to stock discrimination of other coastal marine mammal species.La composition chimique de tissus animaux tels que les dents semble reflĂ©ter l'exposition d'un individu Ă  son milieu gĂ©ochimique. Pour la prĂ©sente Ă©tude, on a utilisĂ© la composition isotopique du plomb (Pb) contenu dans le cĂ©ment pour examiner la structure du stock du morse de l'Atlantique (Odobenus rosmarus rosmarus) dans l'Arctique canadien et le Groenland. Les 12 communautĂ©s qui ont fourni les Ă©chantillons de morse pour ce projet reprĂ©sentent la majoritĂ© des villages canadiens et groenlandais oĂč le morse constitue toujours une grande partie du rĂ©gime alimentaire traditionnel des Inuits. Des diffĂ©rences marquĂ©es entre les sites dans la moyenne des rapports isotopiques du Pb et le faible recoupement des gammes de valeurs rĂ©vĂšlent que chaque village prĂ©levait des morses au sein de troupeaux qui exploitaient des habitats gĂ©ologiques/gĂ©ographiques bien distincts. Cette sĂ©grĂ©gation gĂ©ographique fondĂ©e sur des signatures isotopiques suggĂšre que la plupart des stocks de morses (c.-Ă -d. le groupe de morses qui interagit avec les chasseurs dans chaque communautĂ©) sont plus localisĂ©s dans leur territoire qu'on ne le pensait auparavant. 208Pb/207Pb et 208Pb/204Pb Ă©taient les grands caractĂšres discriminants des stocks, reflĂ©tant l'influence de la composition gĂ©ologique locale Th/U (c-Ă -d. 208Pb) sur la composition isotopique du Pb dans les dents du morse. Les rapports isotopiques fondĂ©s sur 204Pb Ă©taient constamment plus Ă©levĂ©s (plus radiogĂ©niques) et plus homogĂšnes que ceux du substratum terrestre, la diffĂ©rence Ă©tant probablement due Ă  la lixiviation sĂ©lective du Pb radiogĂ©nique passant des phases minĂ©rales dans l'eau de mer et Ă  son mĂ©lange durant la mĂ©tĂ©orisation et le transport. Les signatures isotopiques du plomb dentaire peuvent avoir de vastes applications dans la discrimination des stocks d'autres espĂšces de mammifĂšres marins cĂŽtiers

    A Comparison of Modern and Preindustrial Levels of Mercury in the Teeth of Beluga in the Mackenzie Delta, Northwest Territories, and Walrus at Igloolik, Nunavut, Canada

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    Mercury (Hg) concentrations were compared in modern and preindustrial teeth of belugas (Delphinapterus leucas) and walrus (Odobenus rosmarus rosmarus) at sites in the Canadian Arctic so that the relative amounts of natural and anthropogenic Hg in modern animals could be estimated. Mercury levels in the teeth of Beaufort Sea belugas captured in the Mackenzie Delta, Northwest Territories, in 1993 were significantly (p = 0.0001) higher than those in archeological samples dated A.D. 1450-1650. In terms of geometric means, the Hg levels in modern animals were approximately four times as high as preindustrial levels in 10-year-old belugas, rising with age to 17 times as high in 30-year-olds. Because Hg levels in modern teeth were highly correlated with those in soft tissues, including muscle and muktuk, which are part of traditional human diets, it is likely that soft-tissue Hg has increased to a similar degree over the past few centuries. The increase was not due to dietary differences over time, as shown by analysis of stable-C and -N isotopes in the teeth, and was unlikely to be due to sex differences or to chemical diagenesis of historical samples. Industrially related Hg inputs to the Arctic Ocean and Canadian Arctic Archipelago may be the most likely explanation for the increase. If so, then 80-95% of the total Hg in modern Beaufort Sea belugas more than 10 years old may be attributed to anthropogenic activities. In contrast, tooth Hg concentrations in walrus at Igloolik, Nunavut, were no higher in the 1980s and 1990s than in the period A.D. 1200-1500, indicating an absence of industrial Hg in the species at this location.On a comparĂ© les concentrations de mercure (Hg) dans des dents de bĂ©lugas (Delphinapterus leucas) et de morses (Odobenus rosmarus rosmarus) de notre Ă©poque et de l'Ăšre prĂ©industrielle, Ă  des lieux situĂ©s dans l'Arctique canadien de façon Ă  estimer les montants relatifs de Hg naturel et anthropique chez les individus contemporains. Les niveaux de mercure dans les dents de bĂ©lugas de la mer de Beaufort capturĂ©s en 1993 dans le delta du Mackenzie (Territoires du Nord-Ouest) Ă©taient sensiblement (p = 0,0001) plus Ă©levĂ©s que ceux des Ă©chantillons archĂ©ologiques remontant Ă  une pĂ©riode situĂ©e entre 1450 et 1650 de notre Ăšre. En termes de moyenne gĂ©omĂ©trique, les niveaux de Hg chez les animaux actuels Ă©taient prĂšs de quatre fois plus Ă©levĂ©s que les niveaux prĂ©industriels chez les bĂ©lugas ĂągĂ©s de 10 ans, augmentant avec l'Ăąge jusqu'Ă  ĂȘtre 17 fois plus Ă©levĂ©s chez les bĂ©lugas de 30 ans. Vu que le niveau de Hg dans les dents actuelles Ă©tait fortement corrĂ©lĂ© Ă  celui des tissus mous - y compris les muscles et le muktuk, qui font partie de l'alimentation humaine traditionnelle -, il est probable que la concentration de Hg dans les tissus mous a subi une augmentation similaire au cours des derniers siĂšcles. Comme le montre l'analyse des isotopes de calcium stable et d'azote stable trouvĂ©s dans les dents, cette augmentation n'Ă©tait pas due Ă  des diffĂ©rences alimentaires au cours des annĂ©es, et elle n'Ă©tait probablement pas causĂ©e par la diffĂ©rence de sexe ou la diagenĂšse chimique d'Ă©chantillons historiques. L'explication la plus plausible de l'augmentation est l'apport de Hg industriel dans l'ocĂ©an Arctique et l'archipel Arctique. Si tel est le cas, on pourrait attribuer entre 80 et 95 p. cent du Hg total prĂ©sent chez le bĂ©luga actuel de la mer de Beaufort aux activitĂ©s anthropiques. En revanche, les concentrations de Hg dans les dents de morses provenant d'Igloolik (Nunavut) n'Ă©taient pas plus Ă©levĂ©es dans les annĂ©es 1980 et 1990 qu'au cours de la pĂ©riode situĂ©e entre 1200 et 1500 apr. J.-C., signalant ainsi l'absence de Hg industriel chez cette espĂšce Ă  cet endroit

    Arctic Sentinels: Global mercury emissions have stabilized over the past decade, yet levels in Arctic marine mammals have risen by an order of magnitude. Scientists struggle to explain why.

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    Global mercury emissions have stabilized over the past decade, yet levels in Arctic marine mammals have risen by an order of magnitude. Scientists struggle to explain why

    Exceptionally low mercury concentrations and fluxes from the 2021 and 2022 eruptions of Fagradalsfjall volcano, Iceland

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    Mercury (Hg) is naturally released by volcanoes and geothermal systems, but the global flux from these natural sources is highly uncertain due to a lack of direct measurements and uncertainties with upscaling Hg/SO2 mass ratios to estimate Hg fluxes. The 2021 and 2022 eruptions of Fagradalsfjall volcano, southwest Iceland, provided an opportunity to measure Hg concentrations and fluxes from a hotspot/rift system using modern analytical techniques. We measured gaseous Hg and SO2 concentrations in the volcanic plume by near-source drone-based sampling and simultaneous downwind ground-based sampling. Mean Hg/SO2 was an order of magnitude higher at the downwind locations relative to near-source data. This was attributed to the elevated local background Hg at ground level (4.0 ng m-3) likely due to emissions from outgassing lava fields. The background-corrected plume Hg/SO2 mass ratio (5.6 × 10-8) therefore appeared conservative from the near-source to several hundred meters distant, which has important implications for the upscaling of volcanic Hg fluxes based on SO2 measurements. Using this ratio and the total SO2 flux from both eruptions, we estimate the total mass of gaseous Hg released from the 2021 and 2022 Fagradalsfjall eruptions was 46 ± 33 kg, equivalent to a flux of 0.23 ± 0.17 kg d-1. This is the lowest Hg flux estimate in the literature for active open-conduit volcanoes, which range from 0.6 to 12 kg d-1 for other hotspot/rift volcanoes, and 0.5-110 kg d-1 for arc volcanoes. Our results suggest that Icelandic volcanic systems are fed from a particularly Hg-poor mantle. Furthermore, we demonstrate that the aerial near-source plume Hg measurement is feasible with a drone-based active sampling configuration that captures all gaseous and particulate Hg species, and recommend this as the preferred method for quantifying volcanic Hg emissions going forward

    Toward an assessment of the global inventory of present-day mercury releases to freshwater environments

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    Aquatic ecosystems are an essential component of the biogeochemical cycle of mercury (Hg), as inorganic Hg can be converted to toxic methylmercury (MeHg) in these environments and reemissions of elemental Hg rival anthropogenic Hg releases on a global scale. Quantification of effluent Hg releases to aquatic systems globally has focused on discharges to the global oceans, rather than contributions to freshwater systems that affect local exposures and risks associated with MeHg. Here we produce a first-estimate of sector-specific, spatially resolved global aquatic Hg discharges to freshwater systems. We compare our release estimates to atmospheric sources that have been quantified elsewhere. By analyzing available quantitative and qualitative information, we estimate that present-day global Hg releases to freshwater environments (rivers and lakes) associated with anthropogenic activities have a lower bound of ~1000 Mg· a−1. Artisanal and small-scale gold mining (ASGM) represents the single largest source, followed by disposal of mercury-containing products and domestic waste water, metal production, and releases from industrial installations such as chlor-alkali plants and oil refineries. In addition to these direct anthropogenic inputs, diffuse inputs from land management activities and remobilization of Hg previously accumulated in terrestrial ecosystems are likely comparable in magnitude. Aquatic discharges of Hg are greatly understudied and further constraining associated data gaps is crucial for reducing the uncertainties in the global biogeochemical Hg budget

    Stable isotope food-web analysis and mercury biomagnification in polar bears ( Ursus maritimus )

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    Mercury (Hg) biomagnification occurs in many ecosystems, resulting in a greater potential for toxicological effects in higher-level trophic feeders. However, Hg transport pathways through different food-web channels are not well known, particularly in high-latitude systems affected by the atmospheric Hg deposition associated with snow and ice. Here, we report on stable carbon and nitrogen isotope ratios, and Hg concentrations, determined for 26, late 19th and early 20th century, polar bear ( Ursus maritimus ) hair specimens, collected from catalogued museum collections. These data elucidate relationships between the high-latitude marine food-web structure and Hg concentrations in polar bears. The carbon isotope compositions of polar bear hairs suggest that polar bears derive nutrition from coupled food-web channels, based in pelagic and sympagic primary producers, whereas the nitrogen isotope compositions indicate that polar bears occupy > fourth-level trophic positions. Our results show a positive correlation between polar bear hair Hg concentrations and ÎŽ 15 N. Interpretation of the stable isotope data in combination with Hg concentrations tentatively suggests that polar bears participating in predominantly pelagic food webs exhibit higher mercury concentrations than polar bears participating in predominantly sympagic food webs.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/73930/1/j.1751-8369.2009.00114.x.pd

    Exceptionally low mercury concentrations and fluxes from the 2021 and 2022 eruptions of Fagradalsfjall volcano, Iceland

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    Mercury (Hg) is naturally released by volcanoes and geothermal systems, but the global flux from these natural sources is highly uncertain due to a lack of direct measurements and uncertainties with upscaling Hg/SO2 mass ratios to estimate Hg fluxes. The 2021 and 2022 eruptions of Fagradalsfjall volcano, southwest Iceland, provided an opportunity to measure Hg concentrations and fluxes from a hotspot/rift system using modern analytical techniques. We measured gaseous Hg and SO2 concentrations in the volcanic plume by near-source drone-based sampling and simultaneous downwind ground-based sampling. Mean Hg/SO2 was an order of magnitude higher at the downwind locations relative to near-source data. This was attributed to the elevated local background Hg at ground level (4.0 ng m−3) likely due to emissions from outgassing lava fields. The background-corrected plume Hg/SO2 mass ratio (5.6 × 10−8) therefore appeared conservative from the near-source to several hundred meters distant, which has important implications for the upscaling of volcanic Hg fluxes based on SO2 measurements. Using this ratio and the total SO2 flux from both eruptions, we estimate the total mass of gaseous Hg released from the 2021 and 2022 Fagradalsfjall eruptions was 46 ± 33 kg, equivalent to a flux of 0.23 ± 0.17 kg d−1. This is the lowest Hg flux estimate in the literature for active open-conduit volcanoes, which range from 0.6 to 12 kg d−1 for other hotspot/rift volcanoes, and 0.5–110 kg d−1 for arc volcanoes. Our results suggest that Icelandic volcanic systems are fed from an especially Hg-poor mantle. Furthermore, we demonstrate that the aerial near-source plume Hg measurement is feasible with a drone-based active sampling configuration that captures all gaseous and particulate Hg species, and recommend this as the preferred method for quantifying volcanic Hg emissions going forward
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