Relationships among dissolved organic matter,iron, and discharge in a moorland stream

Dissolved organic matter (DOM) and iron in a moorland stream were determined at 8-hour intervals over a 6-month period to examine relationships with streamflow. Regression of both solutes on discharge were positive and explained 50–70 per cent of the variance in the solute data, but better predictions were obtained in both cases when a covariate reflecting temporal variation in the relationships was introduced (explained variance 80–90 per cent). Variations in the regression of Fe on DOM were also identified, indicating differences in the complexing power of DOM for Fe and possible variations in the chemical composition of the DOM.     

胜利油气区有机包裹体研究及其在油气勘探中的应用

应用显微光度术、显微傅立叶红外光谱（Ｍｉｃｒｏ－ＦＴ．ＩＲ）和飞行时间二次离子质谱（ＴＯＦ－ＳＩＭＳ）等原位微分析技术并结合均一温度测量对胜利油气区下第三系沙河街组沙三段中有机包裹体进行了研究。区分出两类有机包裹体，即原生有机包裹体和次生有机包裹体。结果表明两类有机包裹体特征不同，二者物质组成、有机质成分及化学结构、热演化程度等差别也较大。结合地质分析表明原生有机包裹体是沙三段烃源岩生成烃类运移产物，具“自生自储”特点，而次生有机包裹体是沙四段烃源岩生成的烃类二次运移的产物。沙三段是沙河街组油气运移和聚集的主要层位，因而是寻找油气资源的主要目标层。研究表明，有机包裹体是研究油气生成、运移、聚集和演化等成藏系统最有效的手段之一，在油气勘探中有重要的应用意义。     

耕作措施对陕西耕作土壤碳储量的影响模拟*

鉴于农业生态系统土壤有机碳(SOC)平衡对中国农业可持续发展的重要性,文章以陕西农业生态系统为对象,整合农业生物地球化学模型(DNDC)与陕西农业地理信息系统数据库,利用陕西地区气象和作物资料,对陕西省2000年作物生长发育和土壤碳循环进行了模型模拟,实例探讨了耕作管理对土壤碳储量的影响,并由此评价生物地球化学模型在气候变化、土壤性质及农业耕作管理措施对土壤碳含量影响方面的预测能力。敏感性分析表明土壤性状,尤其是初始有机碳含量是影响模型区域尺度模拟的最主要敏感因素。区域模拟使用灵敏系数分析法,分别采用敏感因子的最大、最小值驱动模型在每一模拟单元内的运算,以产生一个土壤有机碳变化的范围值,土壤有机碳变化的真实值应以较大机率包含在这一范围内。分析模拟结果可以得出3点结论: 1)2000年陕西耕作土壤总有机碳储量约为103TgC,是一个大气CO₂源,向大气释放碳0.5TgC; 2)提高作物秸秆还田率是提高陕西农田碳库储量的有效可行措施,将作物秸秆还田率从当前的15 ％ 提高到50 ％ 或90 ％ 会使陕西农田土壤从大气CO₂源转变为汇,每年分别增加土壤有机碳库储量0.7TgC或2.1TgC; 3)施用有机农肥(500kg/hm²)也会增加土壤碳输入,从而提高土壤碳储量,使陕西农田系统转变为较弱的碳(C)源,每年可多固定0.2TgC。     

方差技术在生物礁识别中的应用

在海相碳酸盐岩勘探中,生物礁滩的识别对确定储层有利相带具有重要意义.方差技术是检测地下断层、地层不连续变化现象及异常地质体卓有成效的一种技术,这里首先介绍了它的基本原理,然后重点展示和分析该技术在YB生物礁识别,沉积相带刻画中的应用成果,证实其技术优势和良好的应用前景.     

峨嵋玄武岩流体包裹体中铂钯的测定方法研究

峨嵋玄武岩同生流体包裹体在800℃爆裂后，2．0g／L NH4Cl溶液提取流体中Pt、Pd，C-410树脂富集-电感耦合等离子体质谱测定，方法相对误差小于25％。激光拉曼光谱与四级质谱测定包裹体的气液成分结果表明：流体中存在一定量的有机组分，这对Pt、Pd以有机螯合态形式进入流体提供了可能。     

Optical properties of low molecular weight and colloidal organic matter: Application of the ultrafiltration permeation model to DOM absorption and fluorescence

Cross-flow ultrafiltration (CFF) is often used to obtain separation and concentration of colloids from bulk natural water samples. Application of the ultrafiltration permeation model allows the quantitative determination of the low molecular weight material (LMW, < 1 kDa) and colloids in bulk dissolved organic matter (DOM) from measurements of time series permeate samples obtained from CFF. Detailed analysis of a Yukon River water sample shows that DOM absorption coefficient and fluorescence follow the permeation model and that the complex spectral optical properties of LMW DOM can be reconstructed from CFF data. A combination of measured and modeled data indicates that the LMW contribution to bulk DOM optical properties obtained from CFF can be grossly underestimated by the use of a low concentration factor (CF, the ratio of initial sample volume to retentate volume). Even at a relatively high CF of 19, optical properties of LMW DOM calculated from measurements of the retentate or integrated permeate would underestimate true values by 5–36%. In the Yukon River sample, LMW dissolved organic carbon represented 26% of the bulk concentration, but only 3–14% of the colored DOM was in the LMW fraction while 31–33% of bulk DOM florescence was due to LMW DOM. The contrasting optical properties of LMW and colloidal DOM support the concept that analysis of bulk DOM absorption and fluorescence properties reveals information about DOM molecular weight.     

地幔岩流体包裹体的稀土元素初步研究

地幔流体REE的研究有助于了解地幔区域化学不均一性、地幔的富集与亏损等地幔地球化学特征。当前对地幔流体的REE研究，主要是通过对比富CO2包裹体与贫CO2包裹体的地幔岩或地幔矿物的测试分析来间接获得信息。本尝试运用电感耦合等离子体质谱（ICP-MS）和热爆方法，直接测定了长白山地区的地幔捕虏体中流体-熔体包裹体REE含量。初步研究显示流体-熔体包裹体中富含REE，尤其LREE相对富集；REE组成曲线右倾，Eu弱正异常，与地幔岩的寄主玄武岩REE组成特征相似，反映源区地幔岩的交代特征。     

原子荧光光谱法测定化探样品时有机质对As,Sb,Bi的干扰

通过研究黑龙江省森林沼泽景观区有机水系沉积物（泥炭）、土壤中As,Sb,Bi的测定结果，发现样品中的有机质对王水消解氢化物原子荧光法测定上述元素存在极大的干扰，提出采用低温（＜450℃）灰化处理可完全消除干扰。对比研究还发现，过去森林沼泽景观区的区域化探扫面资料中的As,Sb,Bi数据存在问题，应专门对其进行评价研究。     

Hydrochemical behaviour of dissolved nitrogen and carbon in a headwater stream of the Canadian Shield: relevance of antecedent soil moisture conditions

This paper examines the impact of contrasting antecedent soil moisture conditions on the hydrochemical response, here the changes in dissolved nitrogen (NO₃^?, NH₄⁺ and dissolved organic nitrogen (DON)) and dissolved organic carbon (DOC) concentrations, of a first‐order stream during hydrological events. The study was performed in the Hermine, a 5 ha forested watershed of the Canadian Shield. It focused on a series of eight precipitation events (spring, summer and fall) sampled every 2 or 3 h and showing contrasted antecedent moisture conditions. The partition of the eight events between two groups (dry or wet) of antecedent moisture conditions was conducted using a principal component analysis (PCA). The partition was controlled (first axis explained 86% of the variability) by the antecedent streamflow, the streamflow to precipitation ratio Q/P and by the antecedent groundwater depth. The mean H⁺, NO₃^?, NH₄⁺, total dissolved nitrogen and DOC concentrations and electrical conductivity values in the stream were significantly higher following dry antecedent conditions than after wetter conditions had prevailed in the Hermine, although the temporal variability was high (17 to 138%). At the event scale, a significantly higher proportion of the changes in DON, NO₃^?, and DOC concentrations in the stream was explained by temporal variations in discharge compared with the seasonal and annual scales. Two of the key hydrochemical features of the dry events were the synchronous changes in DOC and flow and the frequent negative relationships between discharge and NO₃^?. The DON concentrations were much less responsive than DOC to changes in discharge, whereas NH was not in phase with streamflow. During wet events, the synchronicity between streamflow and DON or NO₃^? was higher than during dry events and discharge and NO₃^? were generally positively linked. Based on these observations, the hydrological behaviour of the Hermine is conceptually compatible with a two‐component model of shallow (DON and DOC rich; variable NO₃^?) and deep (DON and DOC poor; variable NO₃^?) subsurface flow. The high NO₃^? and DOC levels measured at the early stages of dry events reflected the contribution from NO₃^?‐rich groundwaters. The contribution of rapid surface flow on water‐repellent soil materials located close to the stream channel is hypothesized to explain the DOC levels. An understanding of the complex interactions between antecedent soil moisture conditions, the presence of soil nutrients available for leaching and the dynamics of soil water flow paths during storms is essential to explain the fluxes of dissolved nitrogen and carbon in streams of forested watersheds. Copyright © 2007 John Wiley & Sons, Ltd.     

The Moreira Gomes deposit of the Cuiú-Cuiú goldfield: Fluid inclusions and stable isotope constraints and implications for the genesis of granite-hosted gold mineralization in the Tapajós Gold Province,Brazil

Moreira Gomes is a recently discovered deposit (21.7 t Au) of the Cuiú-Cuiú goldfield, Tapajós Gold Province, Amazonian Craton. The mineralized zone is about 1200 m long, 30–50 m wide, and at least 400 m in depth. The zone is controlled by a subvertical, east–west-trending structure that is related to a left lateral strike-slip fault system. The host rocks are predominantly tonalites of the Creporizão Intrusive Suite (1997 ± 2 Ma) of uncertain tectonic setting (magmatic arc or post-collision). Hydrothermal alteration and mineralization are predominantly of the fissure-filling type and locally pervasive. Sericitization, chloritization, sulfidation, silicification, carbonatization and epidotization are the observed alteration types. Pyrite is the predominant sulfide mineral and bears inclusions of chalcopyrite, galena, sphalerite and minor hessite and bismuthinite. Gold occurs predominantly as inclusions in pyrite and subordinately in the free-milling state in quartz veins. Ag, Pb and Bi have been detected by semi-quantitative EDS analysis.Three types of fluid inclusions, hosted in quartz veins and veinlets, have been identified. (1) one- and two-phase CO₂ inclusions; (2) two- and three-phase H₂O–CO₂-salt inclusions, and (3) two-phase H₂O-salt inclusions. The CO₂-bearing types are interpreted as the product of phase separation of an immiscible fluid. This fluid presents low to moderate density, low to moderate salinity (1.6–11.8 wt.% NaCl equivalent) and was trapped at 280° to 350 °C. The chemical system of the aqueous inclusions may contain CaCl₂ and/or MgCl₂, salinity varies from zero to 10.1 wt.% NaCl equivalent. Only locally salinities up to 25% have been recorded. This fluid was trapped between 120° and 220 °C and is interpreted as resulting from mixing of a hotter and more saline aqueous fluid (in part derived from phase separation of the H₂O–CO₂ fluid) with a cooler and dilute aqueous fluid.The δ³⁴S values of pyrite (−0.3‰ to 3.9‰) are probably related to magmatic sulfur. The isotopic composition of inclusion fluids and of the fluid in equilibrium with hydrothermal minerals (quartz, chlorite, and calcite) show δ¹⁸O and δD values that range from +0.5 to +9.8‰, and from −49 to −8‰, respectively. Mineral pairs show equilibrium isotopic temperatures that are compatible with the fluid inclusion homogenization temperatures and with textural relationships of the hydrothermal minerals.Isotopic results combined with mineralogical and fluid inclusion data are interpreted to reflect a magmatic-hydrothermal system that evolved in at least three stages. (1) Exsolution of a CO₂-bearing magmatic fluid between 400 °C and 320–350 °C and up to 2.1 kbar (6 km in depth) followed by phase separation and main precipitation of the hydrothermal assemblage composed of chlorite–sericite–pyrite–quartz-gold. (2) Cooling and continuous exsolution of CO₂ produced a CO₂-depleted and slightly more saline aqueous fluid that was trapped mainly at 250°–280 °C. The predominant hydrothermal assemblage of stage 1 continued to form, but epidote is the main phase at this stage. (3) Mixing of the stage 2 aqueous fluid with a cooler and dilute aqueous fluid of meteoric origin, which was responsible for the main carbonatization phase. The mineralizing fluid was neutral to slightly alkaline and relatively reduced. H₂S (and/or HS^-) might have been the main sulfur species in the fluid and Au(HS)^2- was probably the gold transporting complex. Gold deposition occurred as a consequence of a combination of mechanisms, such as phase separation, mixing and fluid-rock interaction.The Moreira Gomes is a granite-hosted gold deposit that is interpreted to be a product of a magmatic-hydrothermal gold system. The age of ore formation (∼1.86 Ga) is consistent with the final stages of evolution of the widespread high-K, calc-alkaline Parauari Intrusive Suite, although the transitional to predominantly alkaline Maloquinha Intrusive Suite cannot be ruled out. Notwithstanding, the deposit does not show the classic features of (oxidized or reduced) intrusion-related gold deposits of Phanerozoic magmatic arcs.