15 research outputs found

    ODP Site 1224: a missing link in the investigation of seafloor weathering

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    A section of Eocene (46 Ma) upper oceanic crust was recovered at Ocean Drilling Program (ODP) Site 1224 in the northeast Pacific basin. The secondary mineralogy and geochemistry of altered basalts and isotopic composition of Ca-carbonate were studied to determine the extent and nature of alteration at this site. Most basalts are &lt;5% altered to secondary mineral assemblages of Fe-oxyhydroxides, celadonite, saponite, Ca-carbonate, trace pyrite, and rare phillipsite and quartz. Alteration is concentrated within brown and dark gray haloes, which formed adjacent to veins and fractures. Haloes comprise 10% of the core (9% dark gray; 1% brown); veins comprise &lt;1% of the core, with an average of 18 veins per meter of recovered cores. Calculated chemical fluxes, which account for groundmass alteration and the composition and abundance of secondary minerals associated with veins, vesicles, and haloes, indicate significant additions of Si, FeT, Mg, Ca, and CO2 and minor additions of Al, Mn, and Na to the crust. The magnitude of these fluxes is low relative to other drilled volcanic sections such as Sites 504, 896, 417, and 418. 87Sr/86Sr ratios (0.70776 to 0.70824) and trace element ratios (Mg/Ca) of calcite imply that Ca-carbonate formed within 20 Ma of crustal formation from relatively unaltered seawater. Oxygen isotope data yield Ca-carbonate formation temperatures of 4 to 11°C. The relative freshness of the Site 1224 lavas is attributed to the capping of the volcanic section by massive flows.<br/

    The regulation of climate engineering

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    Intentional interventions in global physical, chemical, and biological systems on a massive scale are receiving increasing attention in hopes of reducing the threat of anthropogenic climate change. Known as climate engineering, or geoengineering, research is moving forward, but regulation remains inadequate, due in part to significant regulatory challenges. This essay asserts that key to overcoming these regulatory challenges is distinguishing between the two primary forms of climate engineering, and between deployment and research. One of climate engineering's two primary forms, carbon dioxide removal, can largely be addressed through existing legal instruments. In the case of solar radiation management, the other primary form, focusing initially on research can bypass the geopolitical quagmire of deployment. Two other major challenges to developing regulation for solar radiation management research remain: establishing regulatory legitimacy, and developing an appropriate definition of research. Potential regulatory forms include centralized international legal instruments, fully or partially private transnational networks, and norms developed from the bottom up

    The linkage disequilibrium maps of three human chromosomes across four populations reflect their demographic history and a common underlying recombination pattern

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    The extent and patterns of linkage disequilibrium (LD) determine the feasibility of association studies to map genes that underlie complex traits. Here we present a comparison of the patterns of LD across four major human populations (African-American, Caucasian, Chinese, and Japanese) with a high-resolution single-nucleotide polymorphism (SNP) map covering almost the entire length of chromosomes 6, 21, and 22. We constructed metric LD maps formulated such that the units measure the extent of useful LD for association mapping. LD reaches almost twice as far in chromosome 6 as in chromosomes 21 or 22, in agreement with their differences in recombination rates. By all measures used, out-of-Africa populations showed over a third more LD than African-Americans, highlighting the role of the population's demography in shaping the patterns of LD. Despite those differences, the long-range contour of the LD maps is remarkably similar across the four populations, presumably reflecting common localization of recombination hot spots. Our results have practical implications for the rational design and selection of SNPs for disease association studies
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