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181.
Rising atmospheric pCO2 and ocean acidification originating from human activities could result in increased dissolution of metastable carbonate minerals
in shallow-water marine sediments. In the present study, in situ dissolution of carbonate sedimentary particles in Devil’s
Hole, Bermuda, was observed during summer when thermally driven density stratification restricted mixing between the bottom
water and the surface mixed layer and microbial decomposition of organic matter in the subthermocline layer produced pCO2 levels similar to or higher than those levels anticipated by the end of the 21st century. Trends in both seawater chemistry
and the composition of sediments in Devil’s Hole indicate that Mg-calcite minerals are subject to selective dissolution under
conditions of elevated pCO2. The derived rates of dissolution based on observed changes in excess alkalinity and estimates of vertical eddy diffusion
ranged from 0.2 mmol to 0.8 mmol CaCO3 m−2 h−1. On a yearly basis, this range corresponds to 175–701 g CaCO3 m−2 year−1; the latter rate is close to 50% of the estimate of the current average global coral reef calcification rate of about 1,500 g
CaCO3 m−2 year−1. Considering a reduction in marine calcification of 40% by the year 2100, or 90% by 2300, as a result of surface ocean acidification,
the combination of high rates of carbonate dissolution and reduced rates of calcification implies that coral reefs and other
carbonate sediment environments within the 21st and following centuries could be subject to a net loss in carbonate material
as a result of increasing pCO2 arising from burning of fossil fuels. 相似文献
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184.
Previous research has identified the importance of the role of land cover in the global carbon cycle. In particular, forests have been identified as a significant carbon sink that can mitigate the rate of global climate change. Policy makers are faced with complex and difficult challenges in getting timely and useful information in monitoring global forest resources. Recent advances in the tools and methods of forest carbon accounting have produced new, innovative approaches to forest-based carbon inventories. But it is important as new tools are developed that scientists understand the needs of policy makers and that policy makers understand the capabilities and limitations of forest inventory methods. This paper explores four different policy applications that rely, or could benefit from, national carbon inventories. The goal is to help build a bridge between the communities of climate policy makers and scientists specialized in forest carbon inventories. To this end, we pursue three specific objectives: First we provide an overview for policy makers about approaches to forest carbon inventories, paying particular attention to the contributions of remote sensing technologies. Second, we outline the issues particularly relevant to forest inventory scientists who are interested in responding to public policy needs. We then discuss the tradeoffs between information cost, accuracy, precision, transparency and timeliness that need to be balanced in long-term monitoring of forest carbon. Finally, the article concludes with a series of observations and recommendations for the implementation of forest carbon inventories as increasingly central components of global climate change policy. 相似文献
185.
Manuela A. Fehr Per S. Andersson Carl-Magnus Mörth 《Geochimica et cosmochimica acta》2008,72(3):807-826
Holocene sediments from the Gotland Deep basin in the Baltic Sea were investigated for their Fe isotopic composition in order to assess the impact of changes in redox conditions and a transition from freshwater to brackish water on the isotope signature of iron. The sediments display variations in δ56Fe (differences in the 56Fe/54Fe ratio relative to the IRMM-14 standard) from −0.27 ± 0.09‰ to +0.21 ± 0.08‰. Samples deposited in a mainly limnic environment with oxygenated bottom water have a mean δ56Fe of +0.08 ± 0.13‰, which is identical to the mean Fe isotopic composition of igneous rocks and oxic marine sediments. In contrast, sediments that formed in brackish water under periodically euxinic conditions display significantly lighter Fe isotope signatures with a mean δ56Fe of −0.14 ± 0.19‰. Negative correlations of the δ56Fe values with the Fe/Al ratio and S content of the samples suggest that the isotopically light Fe in the periodically euxinic samples is associated with reactive Fe enrichments and sulfides. This is supported by analyses of pyrite separates from this unit that have a mean Fe isotopic composition of −1.06 ± 0.20‰ for δ56Fe. The supply of additional Fe with a light Fe isotopic signature can be explained with the shelf to basin Fe shuttle model. According to the Fe shuttle model, oxides and benthic ferrous Fe that is derived from dissimilatory iron reduction from shelves is transported and accumulated in euxinic basins. The data furthermore suggest that the euxinic water has a negative dissolved δ56Fe value of about −1.4‰ to −0.9‰. If negative Fe isotopic signatures are characteristic for euxinic sediment formation, widespread euxinia in the past might have shifted the Fe isotopic composition of dissolved Fe in the ocean towards more positive δ56Fe values. 相似文献