Smectite formation in metalliferous sediments near the East Pacific Rise at 13°N   总被引：1，自引：0，他引：1  

荣坤波  曾志刚  殷学博  陈帅  王晓媛  齐海燕  马瑶 《海洋学报(英文版)》2018,37(9):67-81

A 43 cm long E271 sediment core collected near the East Pacific Rise(EPR) at 13°N were studied to investigate the origin of smectite for understanding better the geochemical behavior of hydrothermal material after deposition.E271 sediments are typical metalliferous sediments. After removal of organic matter, carbonate, biogenic opal,and Fe-Mn oxide by a series of chemical procedures, clay minerals(2 μm) were investigated by X-ray diffraction,chemical analysis and Si isotope analysis. Due to the influence of seafloor hydrothermal activity and close to continent, the sources of clay minerals are complex. Illite, chlorite and kaolinite are suggested to be transported from either North or Central America by rivers or winds, but smectite is authigenic. It is enriched in iron, and its contents are highest in clay minerals. Data show that smectite is most likely formed by the reaction of hydrothermal Fe-oxyhydroxide with silica and seawater in metalliferous sediments. The Si that participates in this reaction may be derived from siliceous microfossils(diatoms or radiolarians), hydrothermal fluids, or detrital mineral phases. And their δ30 Si values are higher than those of authigenic smectites, which implies that a Si isotope fractionation occurs during the formation because of the selective absorption of light Si isotopes onto Feoxyhydroxides. Sm/Fe mass ratios(a proxy for overall REE/Fe ratio) in E271 clay minerals are lower than those in metalliferous sediments, as well as distal hydrothermal plume particles and terrigenous clay minerals. This result suggests that some REE are lost during the smectite formation, perhaps because their large ionic radii of REE scavenged by Fe-oxyhydroxides preclude substitution in either tetrahedral or octahedral lattice sites of this mineral structure, which decreases the value of metalliferous sediments as a potential resource for REE.  相似文献   

福建李坊重晶石矿床中硅质岩硅、氧同位素组成及成因意义          下载免费PDF全文

陈宪  黎敦朋  崔碧云 《地质找矿论丛》2020,35(2):154-160

福建李坊大型重晶石矿床围岩中发育层状硅质岩,为了研究硅质岩的成因,本文对14件硅质岩样品进行了硅、氧同位素分析。结果表明:δ(~(30)Si)分布范围为-0.3×10~(-3)～+0.1×10~(-3),平均值为-0.1×10~(-3);δ(~(18)O)分布范围为10.6×10-3～18.9×10-3,平均值为14.7×10~(-3)。基于该层状硅质岩的δ(~(30)Si)和δ(~(18)O)分布范围特征,结合野外地质调查研究工作的认识,该硅质岩应为原生沉积成因,二氧化硅来源于热水沉积;根据燧石-海水氧同位素地质温度计估算石英的形成温度为100.2℃—198.7℃,平均值为146.0℃,即该硅质岩形成于热水沉积,暗示李坊重晶石矿床形成于热水沉积作用。  相似文献   

ICP-AES法测定金属硅中硼磷铝锰钙镁铁等28种微量和痕量元素     

乔爱香  江冶  李如燕 《江苏地质》2021,45(4):450-454

采用ICP-AES法对金属硅中的B、P、Al、Mn、Ca、Mg、Fe等28种微量和痕量元素进行分析。根据元素的化学性质制定预处理方法,优化ICP-AES光谱仪测试样品的最佳工作条件。在缺少金属硅标准物质的情况下,选择硅含量较高的国家一级岩石标准物质（GBW07106）进行试验,该标准物质的回收率在95.0%～104.4%之间,相对标准偏差RSD在0.21%～4.01%之间。实际分析工作表明,该方法准确、快速,符合DZ/T 0130—2006的要求。  相似文献   

Targeting carbon dioxide removal in the European Union     

Oliver Geden  Glen P. Peters  Vivian Scott 《Climate Policy》2019,19(4):487-494

In principle, many climate policymakers have accepted that large-scale carbon dioxide removal (CDR) is necessary to meet the Paris Agreement’s mitigation targets, but they have avoided proposing by whom CDR might be delivered. Given its role in international climate policy, the European Union (EU) might be expected to lead the way. But among EU climate policymakers so far there is little talk on CDR, let alone action. Here we assess how best to ‘target’ CDR to motivate EU policymakers exploring which CDR target strategy may work best to start dealing with CDR on a meaningful scale. A comprehensive CDR approach would focus on delivering the CDR volumes required from the EU by 2100, approximately at least 50 Gigatonnes (Gt) CO₂, according to global model simulations aiming to keep warming below 2°C. A limited CDR approach would focus on an intermediate target to deliver the CDR needed to reach ‘net zero emissions’ (i.e. the gross negative emissions needed to offset residual positive emissions that are too expensive or even impossible to mitigate). We argue that a comprehensive CDR approach may be too intimidating for EU policymakers. A limited CDR approach that only addresses the necessary steps to reach the (intermediate) target of ‘net zero emissions’ is arguably more achievable, since it is a better match to the existing policy paradigm and would allow for a pragmatic phase-in of CDR while avoiding outright resistance by environmental NGOs and the broader public.

Key policy insights

• Making CDR an integral part of EU climate policy has the potential to significantly reshape the policy landscape.

• Burden sharing considerations would probably play a major role, with comprehensive CDR prolonging the disparity and tensions between progressives and laggards.

• Introducing limited CDR in the context of ‘net zero’ pathways would retain a visible primary focus on decarbonization but acknowledge the need for a significant enhancement of removals via ‘natural’ and/or ‘engineered’ sinks.

• A decarbonization approach that intends to lead to a low level of ‘residual emissions’ (to be tackled by a pragmatic phase-in of CDR) should be the priority of EU climate policy.

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Evaluating the economic damage of climate change on global coral reefs     

《Global Environmental Change》2015

This paper evaluates the global economic damage arising from the effects of climate change and associated carbon dioxide concentrations on the loss of coral reefs. We do this by first estimating the effects of sea surface temperature and carbon dioxide concentrations on coral cover. We develop a statistical relationship between coral coverage and sea surface temperature that indicates that the effects are dependent on the temperature range. For example, we find that increasing sea surface temperature causes coral coverage to decrease when sea surface temperature is higher than 26.85 °C, with the estimated reduction being 2.3% when sea surface temperature increases by 1%. In addition, we find that a 1% carbon dioxide increase induces a 0.6% reduction in global coral coverage. We also estimate the resultant loss in economic value based on a meta-analysis of the recreational and commercial value of reef coverage and a crude proportional approach for other value factors. The meta-analysis shows that the coral reef value decreases by 3.8% when coral cover falls by 1%. By combining these two steps we find that the lost value in terms of the global coral reef value under climate change scenarios ranges from US$3.95 to US$23.78 billion annually.  相似文献   

二氧化碳洗井中相关问题的探讨     

樊小舟  高波  崔秀忠 《中国煤炭地质》2015,(1):62-65

二氧化碳洗井方法具有设备简单、用时少,效果好的特点,但随着钻孔深度和孔径加大,井管材料的更新换代,有时也会难以出现壮观的井喷场面,达不到理想的洗井效果,使用范围受到限制的问题。总结多年的洗井经验,依据二氧化碳洗井原理,运用洗井过程中起动压力和用气量的计算公式,进而对洗井深度和影响用气量的因素进行了分析,结果表明:1该方法比较适用于井深300m左右、孔径Φ325mm以内、泥浆相对密度小于1.1g/cm3的新打水井,对大于300m的深井,可采用分层洗井法或压风机引喷法进行洗井。2井喷形成时的二氧化碳气体用量,与瓶内气体的压力、钻杆的下入深度、环空体积、地面管路的长度与直径、钻杆内径、钻井液的密度等成正比,而与水温、气温等成反比;当井的含水层的水柱高度低于70m时,一般不易形成井喷。3二氧化碳洗井适用于井内下入钢管、铸铁管等抗压强度较高的井。对水泥管、塑料管等强度较低的井管则要视情况具体分析。  相似文献   

福建云霄晶洞花岗岩及含石榴子石伟晶岩的硅氧同位素研究   总被引：1，自引：0，他引：1  

高建飞  丁悌平 《地质论评》2011,57(5):670-674

在运用常规方法和激光烧蚀同位素分析方法分别对云霄晶洞花岗岩和伟晶岩(长石、石英和石榴子石)的硅、氧同位素组成进行研究的基础上,探讨了晶涧花岗岩及其含石榴子石伟晶岩的物质来源及形成条件.伟晶岩中的石英和长石的氧、硅同位素组成分别较之花岗岩中的石英和长石的氧、硅同位素组成,均未发生明显变化,表明二者岩浆来源一致.云霄县的乌...  相似文献   

Multi-proxy approach (H/H, O/O, C/C and Sr/Sr) for the evolution of carbonate-rich groundwater in basalt dominated aquifer of Axum area, northern Ethiopia     

Tewodros Alemayehu  Albrecht Leis  Anton Eisenhauer  Martin Dietzel 《Chemie der Erde / Geochemistry》2011,(2):177-187

Isotopic and chemical composition of groundwater from wells and springs, and surface water from the basalt-dominated Axum area (northern Ethiopia) provides evidence for the origin of water and dissolved species. Shallow (depth < 40 m) and deep groundwater are distinguished by both chemical and isotopic composition. Deep groundwater is significantly enriched in dissolved inorganic carbon up to 40 mmol l⁻¹ and in concentrations of Ca²⁺, Mg²⁺, Na⁺ and Si(OH)₄ compared to the shallow type.The δ²H and δ¹⁸O values of all solutions clearly indicate meteoric origin. Shifts from the local meteoric water line are attributed to evaporation of surface and spring water, and to strong water–rock interaction. The δ¹³C_DIC values of shallow groundwater between −12 and −7‰ (VPDB) display the uptake of CO₂ from local soil horizons, whereas δ¹³C_DIC of deep groundwater ranges from −5 to +1‰. Considering open system conditions with respect to gaseous CO₂, δ¹³C_DIC = +1‰ of the deep groundwater with highest PCO₂ = 10^−0.9 atm yields δ¹³C_CO2(gas) ≈ −5‰, which is close to the stable carbon isotopic composition of magmatic CO₂. Accordingly, stable carbon isotope ratios within the above range are referred to individual proportions of CO₂ from soil and magmatic origin. The uptake of magmatic CO₂ results in elevated cations and Si(OH)₄ concentrations. Weathering of local basalts is documented by ⁸⁷Sr/⁸⁶Sr ratios of the groundwater from 0.7038 to 0.7059. Highest values indicate Sr release from the basement rocks. Besides weathering of silicates, neoformation of solids has to be considered, which results in the formation of, e.g., kaolinite and montmorillonite. In several solutions supersaturation with respect to calcite is reached by outgassing of CO₂ from the solution leading to secondary calcite formation.  相似文献   

Solar Photocatalytic Decolorization and Detoxification of Industrial Batik Dye Wastewater Using P(3HB)‐TiO2 Nanocomposite Films     

Nanthini Sridewi  Liu‐Tzea Tan  Kumar Sudesh 《洁净——土壤、空气、水》2011,39(3):265-273

Solar photocatalytic decolorization and detoxification of batik dye wastewater using titanium dioxide (TiO₂) immobilized on poly‐3‐hydroxybutyrate (P(3HB)) film was studied. The effects of initial dye concentration, catalyst concentration, P(3HB) film thickness, and fabrication methods of the nanocomposite films were evaluated against methylene blue, a standard organic dye. It was observed that 0.4 g of P(3HB)‐40 wt% TiO₂ removed 96% of the color under solar irradiation. P(3HB) and TiO₂, mixed concurrently in chloroform followed by stirring for 24 h showed a more even distribution of the photocatalyst on the polymer surface and yielded almost 100% color removal. The photocatalytic films were able to completely decolorize real industrial batik dye wastewater in 3 h and induced a chemical oxygen demand (COD) reduction of 80%. Reusability of the 0.4 g P(3HB)‐40 wt% TiO₂ film in decolorizing the batik dye wastewater was also possible as it gave a high consistent value of decolorization percentage (>80%) even after the sixth repeated usage. Recovery step of the photocatalysts was also not required in this simple treatment system. The decolorized batik dye wastewater had less/no toxic effects on mosquito larvae, Aedes aegypti, and microalgae, Scenedesmus quadricauda indicating simultaneous detoxification process along with the decolorization process.  相似文献   

Characterizing the international carbon capture and storage community     

Jennie C. Stephens  Anders Hansson  Yue Liu 《Global Environmental Change》2011,21(2):379-390

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