Differing controls on river‐ and lake‐water hydrogen and oxygen isotopic values in the western United States

Surface water oxygen and hydrogen isotopic values are commonly used as proxies of precipitation isotopic values to track modern hydrologic processes while proxies of water isotopic values preserved in lake and river sediments are used for paleoclimate and paleoaltimetry studies. Previous work has been able to explain variability in USA river‐water and meteoric‐precipitation oxygen isotope variability with geographic variables. These studies show that in the western United States, river‐water isotopic values are depleted relative to precipitation values. In comparison, the controls on lake‐water isotopic values are not well constrained. It has been documented that western United States lake‐water input values, unlike river water, reflect the monthly weighted mean isotopic value of precipitation. To understand the differing controls on lake‐ and river‐water isotopic values in the western United States, we examine the seasonal distribution of precipitation, evaporation and snowmelt across a range of seasonality regimes. We generate new predictive equations based on easily measured factors for western United States lake‐water, which are able to explain 69–63% of the variability in lake‐water hydrogen and oxygen isotopic values. In addition to the geographic factors that can explain river and precipitation values, lake‐water isotopic values need factors related to local hydrologic and climatic characteristics to explain variability. Study results suggest that the spring snowmelt runs off the landscape via rivers and streams, depleting river and stream‐water isotopic values. By contrast, lakes receive seasonal contributions of precipitation in proportion to the seasonal fraction of total annual precipitation within their watershed. Climate change may alter the ratio of snow to rain fall, affecting water resource partitioning between rivers and lakes and by implication of groundwater. Paleolimnological studies must account for the multiple drivers of water isotopic values; likewise, studies based on the isotopic composition of fossil material need to distinguish between species that are associated with rivers versus lakes. Copyright © 2010 John Wiley & Sons, Ltd.     

Root‐related rhodochrosite and concretionary siderite formation in oxygen‐deficient conditions induced by a ground‐water table rise

Sedimentological, mineralogical, stable carbon and oxygen isotope determinations and biomarker analyses were performed on siderite concretions occurring in terrestrial silts to understand their formation and to characterize the sedimentary and diagenetic conditions favouring their growth. High δ¹³C values (6·4‰ on average) indicate that siderite precipitated in an anoxic environment where bacterial methanogenesis operated. The development of anoxic conditions during shallow burial was induced by a change in sedimentary environment from flood plain to swamp, related to a rise of the ground‐water table. Large amounts of decaying plant debris led to efficient oxygen consumption within the pore‐water in the peat. Oxygen depletion, in combination with a decrease in sedimentation rate, promoted anoxic diagenetic conditions under the swamp and favoured abundant siderite precipitation. This shows how a change in sedimentary conditions can have a profound impact on the early‐diagenetic environment and carbonate authigenesis. The concretions contain numerous rhizoliths; they are cemented with calcium‐rhodochrosite, a feature which has not been reported before. The rhodochrosite cement has negative δ¹³C values (?16·5‰ on average) and precipitated in suboxic conditions due to microbial degradation of roots coupled to manganese reduction. The exceptional preservation of the epidermis/exodermis and xylem vessels of former root tissues indicates that the rhodochrosite formed shortly after the death of a root in water‐logged sediments. Rhodochrosite precipitated during the initial stages of concretionary growth in suboxic microenvironments within roots, while siderite cementation occurred simultaneously around them in anoxic conditions. These suboxic microenvironments developed because oxygen was transported from the overlying oxygenated soil into sediments saturated with anoxic water via roots acting as permeable conduits. This model explains how separate generations of carbonate cements having different mineralogy and isotopic compositions, which would conventionally be regarded as cements precipitated sequentially in different diagenetic zones during gradual burial, can form simultaneously in shallow burial settings where strong redox gradients exist around vertically oriented permeable root structures.     

Iron isotopic systematics of UHP eclogites respond to oxidizing fluid during exhumation

The iron stable isotope compositions (δ⁵⁶Fe) and iron valence states of ultrahigh‐pressure eclogites from Bixiling in the Dabie orogen belt, China, were measured to trace the changes of geochemical conditions during vertical transportation of earth materials, for example, oxygen fugacity. The bulk Fe³⁺/ΣFe ratios of retrograde eclogites, determined by Mössbauer spectroscopy, are consistently higher than those of fresh eclogites, suggesting oxidation during retrograde metamorphism and fluid infiltration. The studied eclogites (five samples) display limited mid‐ocean ridge basalts (MORB)‐like (~0.10‰) δ⁵⁶Fe values, which are indistinguishable from their protoliths, that is, gabbro cumulates formed through differentiation of mantle‐derived basaltic magma. This suggests that Fe isotope fractionation during continental subduction is limited. Garnet separates display limited δ⁵⁶Fe variation ranging from ?0.08 ± 0.07 ‰ to 0.02 ± 0.07‰, whereas coexisting omphacite displays a large variation of δ⁵⁶Fe values from 0.15 ± 0.07‰ to 0.47 ± 0.07‰. Omphacite also has highly variable Fe³⁺/ΣFe ratios from 0.367 ± 0.025 to 0.598 ± 0.024, indicating modification after peak metamorphism. Omphacite from retrograde eclogites has elevated Fe³⁺/ΣFe ratios (0.54–0.60) compared to that from fresh eclogites (~0.37), whereas garnet displays a narrow range of ferric iron content with Fe³⁺/ΣFe ratios from 0.039 ± 0.013 to 0.065 ± 0.022. The homogenous δ⁵⁶Fe values and Fe³⁺/ΣFe ratios of garnet suggest that it survived the retrograde metamorphism and preserved its Fe‐isotopic features and ferric contents of peak metamorphism. Because of similar diffusion rates of Fe and Mg in garnet and omphacite, and constant Δ²⁶Mg_{omphacite‐garnet} values (1.14 ± 0.04‰), equilibrium iron isotope fractionation between garnet and omphacite was probably achieved during peak metamorphism. Elevated Fe³⁺/ΣFe ratios of omphacite from retrograde eclogites and variant Δ⁵⁶Fe_{omphacite‐garnet} values of the studied eclogites (0.13 ± 0.10‰ to 0.48 ± 0.10‰) indicate that oxidized geofluid infiltration resulted in the elevation of δ⁵⁶Fe values of omphacite during retrograde metamorphism.     

广西栗木钨锡铌钽矿区流体包裹体及氢氧同位素研究

本文通过对广西栗木矿区金竹源矿床和水溪庙矿床的流体包裹体研究,得出该矿区流体包裹体主要有两相H_2O-NaCl和H_2O-NaCl-CO_2两种类型。显微测温结果表明:两相H_2O-NaCl型流体包裹体均一温度主要集中于181.9~258.8℃,盐度w(Na Cleq)主要集中于4.01%~6.87%,密度0.690~0.988 g/cm3;H_2O-NaCl-CO_2型流体包裹体均一温度为178.5~331.1℃,主要集中在两个温度段,分别为高-中温段(265.3~315.5℃)和中-低温段(202.3~264.1℃),盐度w(NaCleq)主要集中在0.21%~5.05%,密度为0.678~0.886 g/cm3。栗木矿区成矿流体有两个温度集中段,且具有低盐度、低密度的特征。氢氧同位素研究结果表明:金竹源矿床钨锡铌钽矿化花岗岩石英δD值为-73.6‰~-62.8‰,δ~(18)OV-SMOW值为7.5‰~8.9‰,计算得δ~(18)OH2O值为6.00‰~7.40‰;水溪庙矿床钨锡铌钽矿化花岗岩石英δD值为-73.8‰~-58.3‰,δ~(18)OV-SMOW值为11.0‰~13.2‰,计算得δ~(18)OH2O值为9.50‰~11.70‰,水溪庙矿床含钨锡石英脉石英δD值为-75.3‰~-56.6‰,δ~(18)OV-SMOW值为11.8‰~14.1‰,计算得δ~(18)OH2O值为2.20‰~4.50‰。栗木矿区钨锡铌钽矿化花岗岩成矿流体来源于岩浆水,含钨锡石英脉成矿流体来源于岩浆水和大气降水的混合流体。     

Dynamic responses of atmospheric carbon dioxide concentration to global temperature changes between 1850 and 2010

Changes in Earth's temperature have significant impacts on the global carbon cycle that vary at different time scales, yet to quantify such impacts with a simple scheme is traditionally deemed difficult. Here, we show that, by incorporating a temperature sensitivity parameter(1.64 ppm yr~(-1) ?C~(-1)) into a simple linear carbon-cycle model, we can accurately characterize the dynamic responses of atmospheric carbon dioxide(CO_2) concentration to anthropogenic carbon emissions and global temperature changes between 1850 and 2010(r~2 0.96 and the root-mean-square error 1 ppm for the period from 1960onward). Analytical analysis also indicates that the multiplication of the parameter with the response time of the atmospheric carbon reservoir(～12 year) approximates the long-term temperature sensitivity of global atmospheric CO_2concentration(～15 ppm?C~(-1)), generally consistent with previous estimates based on reconstructed CO_2 and climate records over the Little Ice Age. Our results suggest that recent increases in global surface temperatures, which accelerate the release of carbon from the surface reservoirs into the atmosphere, have partially offset surface carbon uptakes enhanced by the elevated atmospheric CO_2 concentration and slowed the net rate of atmospheric CO_2 sequestration by global land and oceans by ～30%since the 1960 s. The linear modeling framework outlined in this paper thus provides a useful tool to diagnose the observed atmospheric CO_2 dynamics and monitor their future changes.     

Incorporation of a dynamic root distribution into CLM4.5: Evaluation of carbon and water fluxes over the Amazon

Roots are responsible for the uptake of water and nutrients by plants and have the plasticity to dynamically respond to different environmental conditions. However, most land surface models currently prescribe rooting profiles as a function only of vegetation type, with no consideration of the surroundings. In this study, a dynamic rooting scheme, which describes root growth as a compromise between water and nitrogen availability, was incorporated into CLM4.5 with carbon–nitrogen(CN) interactions(CLM4.5-CN) to investigate the effects of a dynamic root distribution on eco-hydrological modeling. Two paired numerical simulations were conducted for the Tapajos National Forest km83(BRSa3) site and the Amazon, one using CLM4.5-CN without the dynamic rooting scheme and the other including the proposed scheme. Simulations for the BRSa3 site showed that inclusion of the dynamic rooting scheme increased the amplitudes and peak values of diurnal gross primary production(GPP) and latent heat flux(LE) for the dry season, and improved the carbon(C) and water cycle modeling by reducing the RMSE of GPP by 0.4 g C m~(-2)d~(-1), net ecosystem exchange by 1.96 g C m~(-2)d~(-1), LE by 5.0 W m~(-2), and soil moisture by 0.03 m~3m~(-3), at the seasonal scale, compared with eddy flux measurements, while having little impact during the wet season. For the Amazon, regional analysis also revealed that vegetation responses(including GPP and LE) to seasonal drought and the severe drought of 2005 were better captured with the dynamic rooting scheme incorporated.     

变分同化框架通过背景误差协方差构建动力平衡约束的研究进展

通过背景误差协方差构建动力平衡约束是变分同化框架设计的重要环节。它不仅帮助实现变量间的协同分析,提高观测使用效率,还能改善变分极小化问题的性状。本文在系统梳理通过背景误差协方差引入动力平衡约束的方式、流程的基础上,对求解目前全球和有限区域变分同化系统普遍采用的准地转平衡和静力平衡约束的共性问题和存在的不足作了归纳总结。分析了求解准地转平衡约束的三类方案:动力平衡方程方案、统计方案和动力-统计相结合方案的优缺点。对照比较了不同垂直离散方案下求解静力平衡约束时遇到的欠定问题的表现以及解决途径。最后,展望了基于背景误差协方差构建动力平衡约束在赤道等特殊地区、高分辨率同化系统、以及集合-变分混合同化系统发展中面临的挑战和机遇。     

内蒙古河套灌区春玉米作物系数试验研究

作物系数曲线是估算作物生长季耗水量变化的重要参数。基于2013年4—9月内蒙古巴彦淖尔市临河区田间水分试验和1994—2013年气象站观测资料,利用水量平衡法反求春玉米作物系数,分析生长季内的变化规律, 建立动态模拟方程,并与联合国粮农组织 (FAO) 分段直线法结果进行比较, 提出胁迫条件下作物系数的叶面积修正方法。结果表明:玉米作物系数随发育进程可用三项式曲线描述,变化趋势与产量水平无关, 但随产量增高而变幅增大;以出苗后相对积温为时间变量建立模拟方程效果较好,决定系数 (R2) 均在0.92以上;模拟计算出各站点最大 (1.30~1.48) 和平均 (0.831~0.919) 作物系数,与FAO分段直线法计算的典型值和区间值基本一致,生长中期平均相对误差为3.4%~7.2%;提出利用相对叶面积指数修正作物系数的计算方法;通过2014年实例检验,土壤水分模拟值与实测值的平均相对误差为6.3%,相对误差小于15%的占95.8%。     

Comparative assessment of Japan's long-term carbon budget under different effort-sharing principles

This article assesses Japan's carbon budgets up to 2100 in the global efforts to achieve the 2?°C target under different effort-sharing approaches based on long-term GHG mitigation scenarios published in 13 studies. The article also presents exemplary emission trajectories for Japan to stay within the calculated budget.

The literature data allow for an in-depth analysis of four effort-sharing categories. For a 450?ppm CO₂e stabilization level, the remaining carbon budgets for 2014–2100 were negative for the effort-sharing category that emphasizes historical responsibility and capability. For the other three, including the reference ‘Cost-effectiveness’ category, which showed the highest budget range among all categories, the calculated remaining budgets (20th and 80th percentile ranges) would run out in 21–29 years if the current emission levels were to continue. A 550?ppm CO₂e stabilization level increases the budgets by 6–17 years-equivalent of the current emissions, depending on the effort-sharing category. Exemplary emissions trajectories staying within the calculated budgets were also analysed for ‘Equality’, ‘Staged’ and ‘Cost-effectiveness’ categories. For a 450?ppm CO₂e stabilization level, Japan's GHG emissions would need to phase out sometime between 2045 and 2080, and the emission reductions in 2030 would be at least 16–29% below 1990 levels even for the most lenient ‘Cost-effectiveness’ category, and 29–36% for the ‘Equality’ category. The start year for accelerated emissions reductions and the emissions convergence level in the long term have major impact on the emissions reduction rates that need to be achieved, particularly in the case of smaller budgets.

Policy relevance

In previous climate mitigation target formulation processes for 2020 and 2030 in Japan, neither equity principles nor long-term management of cumulative GHG emissions was at the centre of discussion. This article quantitatively assesses how much more GHGs Japan can emit by 2100 to achieve the 2?°C target in light of different effort-sharing approaches, and how Japan's GHG emissions can be managed up to 2100. The long-term implications of recent energy policy developments following the Fukushima nuclear disaster for the calculated carbon budgets are also discussed.     

从平衡-封闭-静态转向非平衡-开放-动力学研究-热液矿床成因的若干新概念概述

热液金属矿床成因研究过程中,观测与实验始终是密切结合的。上世纪70年代,平衡热力学的实验数据的快速积累,使人们用热力学理论计算可以预测和反演矿石和岩石的成因。但是,没有矿物-水溶液的反应速率数据,又没有与流体力学的结合,搞清楚矿石成因是困难的。七、八十年代,开始研究矿物与水溶液的反应动力学实验。科学家们开始瞄准了从平衡-封闭-静态转向非平衡-开放-动力学研究的这个大方向。1992年我们建立地球化学动力学开放研究实验室。研究高温高压矿物与水反应速率,发现固液的开放体系的自组织现象。实验发现温度影响矿物的各个元素反应速率改变,发现在跨越水临界态时矿物与水反应速率涨落、在近临界的气-液两相不混溶区一些金属进入气相、超临界流体的氧化作用及特别的溶剂性能影响矿物溶解性质。实验证实:临界态区流体与矿石成因有关。水岩相互作用的反应动力学实验温度从低温到550度,揭示矿石的金属来源、迁移、金属与蚀变分带机制。一大批大于300度的矿物与水反应动力学实验在国际界是少有报道的。九十年代,超高压的科学发展,与同步辐射光源的技术进步的结合,使固体地球科学又迈向了地球深内部。我们发展了高温高压流体性质的原位直测(测量850℃水溶液)红外谱,发现深部流体的新性质:气液两相流体的新结构,在临界温度区(300~400℃),水分子氢键网络的破坏受压力影响不大(23MPa~3GPa),同时,出现水的高电导率。研发新仪器为开放-流动-非平衡的反应动力学实验与极端条件下物质性质的直接观测结合,在科学前沿领域开辟了创新道路。