Environmental Redox Changes of the Ancient Sea in the Yangtze Area during the Ordo-Silurian Transition     

YAN Detian  CHEN Daizhao  WANG Qingchen  WANG Jianguo  CHU Yang 《《地质学报》英文版》2008,82(3):679-689

Extensive organic-matter （OM） rich facies （black shales） occur in the Ordo-Silurian boundary successions in the Yangtze area, South China. To investigate the redox changes of the Yangtze Sea during the Ordo-Silurian transition, two OM sections （Wangjiawan in Yichang, Hubei Province, and Sanjiaguan in Zhangjiajie, Hunan Province） straddling the Ordo-Silurian boundary are studied. The measurements finished in this study include contents of the total organic carbon （TOC）, pyrite sulphur, and different species of Fe, including dithionite-extractable Fe （FED）, pyrite Fe （FeP）, HCl-extractable Fe （FeH）, and total Fe （FeT）, in black shales, as well as other redox proxies, such as the SIC ratio, the ratio between highly reactive Fe （FeHR = FeD ＋ FeP） and FeT, and the FeP/（FeP ＋ FeH） ratio, known as the degree of pyritization （DOP）. In the Wangjiawan section, the Middle Ashgill sediments have high FeHR/FeT ratios （0.20-0.77; avg. 0.45）, high DOP values （0.21-0.72; avg. 0.54）, and a relatively constant sulfur content independent of the organic carbon content. By the contrast, the mid-early Hirnantian deposits generally have low FeHR/FeT ratios （0.10-0.35; avg. 0.21）, low DOP values （0.11- 0.40; avg. 0.28）, and SIC values are clustering on the normal marine value （SIC = 0.36）. The late Hirnantian and early Rhuddanian deposits, similar to those of the Middle Ashgill deposits, are characterized by high FeHR/FeT ratios （0.32-0.49; avg. 0.41）, high DOP values （0.46-0.68; avg. 0.53） and fairly constant sulfur contents. These data suggest the occurrences of marine anoxia on the Yangtze Sea shelf during intervals of the Mid Ashgill, Late Hirnantian and Early Rhuddanian, and ventilated and oxygenated marine conditions during the mid-early Hirnantian time. The mid-early Hirnantian ventilated event was concomitant with the global glacial period, likely resulted from the glacio-eustatic sea-level fall and subsequent circulation of cold, dense oxygenated waters  相似文献   

青海省柴达木盆地西北缘盐类矿产遥感预测研究     

张彤蕴  朱谷昌  杨自安  石菲菲  张建国 《矿产与地质》2008,22(6):551-555

利用ETM多光谱遥感图像,在对盐湖区的遥感影像特征和主要地物光谱特征分析的基础上,通过波段组合变换,压抑粘土及砂砾层等地物的影响,将盐类矿产信息增强提取出来。对比前人的钾盐矿田勘查成果,所提取的盐类信息异常与现代新盐带、湿盐滩和现正在开采的钾盐矿区十分吻合。结合区域地质背景与成矿条件的分析研究,圈定了4个预测区、9处有利地段,为进一步盐类矿产勘查提供了科学依据和目标地。  相似文献   

石笋流体包裹体中的惰性气体及其在重建长江中游古温度变化中的作用   总被引：2，自引：0，他引：2  

方念乔  胡超涌 《地学前缘》2008,15(4):132-137

文中讨论了一种评估古气温变化的新方法。我们成功地利用石笋流体包裹体所捕获的Xe/Ar比值,重建了末次冰盛期以来盛行东亚季风的长江中游地区的气候演化。一种表达成ln(CXe/CAr)的对数式被证明与冷暖周期变化具有密切的关系。从研究的石笋中所提出的δ13C与Mg/Ca曲线一般随区域古气温波动而变化,但不能排除其中有另类气候信号的叠加。我们的工作则明确地指出,流体包裹体所记录的Xe/Ar在各种反映温度变化的替代指标中可能是最好的一种。整体而言,ln(CXe/CAr)曲线与那些基本随暖期和冷期振荡的曲线保持一致。将稀有气体曲线与δ13C和Mg/Ca信号整合对比之后,我们在研究区划分出末次冰盛期以来8组暖/冷旋回。整合后的气温变化模式合理地解释了过去20000年里的区域环境变化。  相似文献   

安徽省××地区富硒土壤地球化学评价     

邢润华  贾十军 《安徽地质》2008,18(3)

安徽省××地区土壤Se含量>0.4mg/kg的面积100km2,富硒土壤受湖泊沉积环境控制.富硒区土壤环境质量低于土壤三级标准限值,农业营养元素K20、N、有机质丰富.精米Se含量>0.04mg/kg,高于对比区两倍,重金属元素未超标.  相似文献   

中国西南地区二叠纪乐平世陆生生物大灭绝期煤中砷和硒的演化及古环境意义   总被引：1，自引：1，他引：0       下载免费PDF全文

雒昆利  李会杰  牛彩香  陈同斌 《古地理学报》2008,10(4):385-394

为了探讨中国西南地区二叠系乐平统(上二叠统)龙潭组中下部煤系不同煤组分中砷、硒的含量和演化及古环境意义,对近10年来采集于中国西南扬子地台的二叠系乐平统龙潭组主采煤层的原煤、亮煤、煤矸石、黄铁矿结核等样品中砷、硒元素含量进行了测定和分析,并与中国华北地台一些煤矿的上石炭统-下二叠统太原组、山西组的原煤、镜煤、亮煤、煤矸石、黄铁矿结核等样品中砷、硒含量进行对比分析。结果表明：西南地区乐平统龙潭组煤的砷、硒含量变化较大,但总体高于华北晚石炭世和早二叠世煤的砷、硒含量;西南二叠系乐平统龙潭组大多数的亮煤中砷、硒含量高于原煤全煤样(刻槽样)中的砷、硒含量,也远远高于同煤层煤矸石的含量,龙潭组部分亮煤的砷含量尤其高,为55～338 mg/kg,还发现砷含量为89 mg/kg的亮煤。但华北上石炭统-下二叠统的镜煤中的砷、硒含量与之相反,低于原煤全煤样的砷、硒含量,其中砷含量非常低,为063～129 mg/kg。说明西南地区上二叠统煤中的砷和硒与煤的有机质密切相关,可能主要来源于成煤古植物。在西南乐平世早、中期第Ⅰ幕陆生生物集群灭绝事件期间,陆生动物的食物--植物中有毒有害元素砷、硒含量明显增加,陆生环境或泥炭沼泽中可溶性砷、硒含量增加。  相似文献   

硫铅酸盐“S”型瞬凝水泥干法护壁堵漏技术研究          下载免费PDF全文

彭振斌 《探矿工程》1995,(2):41-42,60

介绍了硫铝酸盐“Ｓ”型瞬凝水泥干法者漏时使用的配方,阐述了输送工具和扫孔钻具的设计以及灌注工艺技术。  相似文献   

Sulfur Isotope Fractionation in Magmatic Systems：Models of Rayleigh Distillation and Selective Flux   总被引：2，自引：0，他引：2  

郑永飞 《中国地球化学学报》1990,9(1):27-45

The effect of Rayleigh distillation by outgassing of SO2 and H2S on the isotopic composition of sulfur remaining in silicate melts is quantitatively modelled.A threshold mole fraction of sulfur in sulfide component of the melts is reckoned to be of critical importance in shifting the δ^34S of the melts mith respect to the original magmas.The partial equilibrium fractionation in a magmatic system is evaluated by assuming that a non-equilibrium flux of sulfur occurs between magmatic volatiles and the melts,while an equilibrium fractionation is approached between sulfate and sulfide within the melts.The results show that under high fo2 conditions,the sulfate/sulfide ratio in a melt entds to increase,and the δ^34S value of sulfur in a solidified rock might then be shifted in the positive direction.This may either be due to Rayleigh outgassing in case the mole fraction of sulfide is less than the threshold,or due to a unidirectional increase in δ^34S value of the sulfate with decreaing temperature,Conversely,at low fo2,the sulfate/sulfide ratio tends to decrease and the δ^34S value of total sulfur could be driven in the negative direction,either because of the Rayleigh outgassing in case the mole fraction of sulfide is greater than the threshold,or because of a unidirectional decrease inδ^34S value of the sulfide.To establish isotopic equilibrium between sulfate and sulfide,the HM,QFM or WM buffers in the magmatic system are suggested to provide the redox couple that could simultaneously reduce the sulfate and oxidize the sulfide.CaO present in the silicatte Melts is also called upon to participate in the chemical equilibrium between sulfate and sulfide,Consequently,the δ^34S value of an igneous rock could considerably deviate from that of its original magma due to the influence of oxygen fugacity and temperature at the time of magma solidification.  相似文献   

使用价值分析优化方法在功能—技术矩阵求解中的应用     

罗庆生  韩宝玲 《武汉大学学报(信息科学版)》1990,(2)

功能—技术矩阵,经众多工作者的努力研究,已渐趋成熟与实用。但如何利用功能—技术矩阵构造在广义现代设计领域中适用的科学模式,解决多学科设计方案的组成与评价问题,还存在薄弱环节。本文利用“使用价值分析优化”的概念,从设计方案技术先进性和经济合理性的协调统一的角度出发,较好地实现了功能—技术矩阵可行优化组合链的组成与评价,弥补了以往的缺陷。  相似文献   

Selenium contamination in the Colorado River Basin, western USA： Remediation by leaching and nanof＇dtration membranes     

YousifK. Kharaka Evangelos G. Kakouros James J. Thordsen David L. Naftz 《中国地球化学学报》2006,25(B08):100-101

Selenium （Se） is an essential micronutrient to biota, but can become a potent toxicant at elevated concentrations. The natural sources and chemical properties of Se species make the boundary between deficiency and toxicity narrow for some biota, with both phenomena common around the globe. Large areas of farmland in the Colorado River Basin （CRB） generate salinized drainage water with Se concentrations much higher than 5 μg/L, the U.S. Environmental Protection Agency chronic water-quality criterion for the protection of aquatic life. We have carried out detailed field and laboratory studies to investigate Se geochemistry and remediation in two of these areas： the Middle Green River Basin, Utah and the Salton Sea Basin, California, located respectively in the Upper and Lower CRB. Results from these and other studies show that approximately 90% of the dissolved Se in the Colorado River and its tributaries originally is derived from the Upper Cretaceous Mancos Shale and equivalent pyritic marine units that outcrop in the Upper CRB. Selenium is mobilized commonly by biogeochemical oxidation of this pyritic shale and is concentrated mainly as selenate （SeO4^2-） in soils and agricultural drainage water of dry climates by evaporation. Minor （0%-5%） amounts of Se are present as the selenite species （HSeO3^-） and （SEO3^2-）, but these species and the more reduced species, elemental Se （SeO） and selenide （Se^2-）, have much lower solubility and/or have high sorptive affinity towards organic matter, clay minerals and iron oxyhydroxides. The concentration of dissolved Se （-2.5 μg/L） and salinity in the Lower Colorado River water are among the highest of the world major rivers. Because of low precipitation （7 cm/a） and extreme evapotranspiration （-1.8 m/a） rates in the Salton Sea Basin, California, Se values in irrigation water imported from the Colorado River increase to 〉300 μg/L in drainage wastewater. Removal of Se from contaminated wastewater by nanofiltration membranes was demonstrated in laboratory and pilot-scale field experiments.  相似文献   

Determination of total selenium in geological samples by HG-AFS？ After enrichment with thiol cotton fiber     

《中国地球化学学报》2006,25(B08):208-209

  相似文献