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   

基于穆斯堡尔谱技术的铁化学种及其在相关表生地球科学研究中的应用   总被引：4，自引：3，他引：1  

郑国东 《矿物岩石地球化学通报》2008,27(2)

由于铁元素分布的广泛性和化学反应的活泼性,它在地球科学研究中具有极为重要的应用意义。与其他多种方法相比较,穆斯堡尔技术是铁元素化学种检测最为有效的方法之一,许多研究结果显示铁元素化学种在相关表生坩球科学研究中的应用前景广阔,例如滑坡带地球化学、湖泊沉积环境、岩石光谱特征、重金属污染沉积物及其环境修复技术等。  相似文献   

滇西沘江流域水体中重金属元素的地球化学特征   总被引：6，自引：1，他引：5  

李瑞萍  王安建  曹殿华  王高尚  李以科  耿诺 《地质通报》2008,27(7):1071-1078

通过测定流经兰坪金顸铅锌矿区的沘江水体中Pb、Zn、Cd、As的含量和底泥中重金属元素的化学形态的含量,分析了重金属元素的分布和化学形态的变化。结果表明,沘江水遭到了Cd污染,底泥已经成为重金属元素的蓄积库,以国家土壤环境质量标准（Ⅲ级）衡量,Pb、Zn、Cd和舡分别超标3．4倍、15．8倍、106倍和2．6倍。沘江水中重金属元素含量的峰值在矿山附近的下游,而底泥中重金属元素的峰值在矿山下游30-50km的地方,矿业活动、水流变缓、pH等水体环境条件的变化都能影响水和底泥中重金属元素的含量。底泥中的Pb以碳酸盐结合态为主,Zn和Cd以铁锰氧化物结合态为主,而As以残渣态为主。Pb、Cd、Zn三种元素的环境有效态含量比较高,对沘江流域生态环境具有潜在的巨大的危害。  相似文献   

塔里木克拉通东北缘二叠纪镁铁质岩浆氧化物与硫化物成矿条件对比     

徐文博  张铭杰  包亚文  满毅  李思奥  王鹏 《地质学报》2022,96(12):4257-4274

塔里木克拉通东北缘坡北、磁海等地二叠纪幔源岩浆活动形成了镍钴硫化物矿床和铁钴氧化物矿床，两者赋矿镁铁 超镁铁岩体的年龄相近(290~260 Ma)，主、微量元素和Sr Nd Hf同位素组成相似，分配系数接近的微量元素比值分布于相同趋势线，揭示两者岩浆源区相同，可能为俯冲板片流体交代的亏损地幔或软流圈地幔。两类矿床镁铁 超镁铁质岩中Co与Ni含量正相关，Co主要富集在基性程度高的岩石中；块状硫化物与磁铁矿矿石中Co与Ni相关性差，Co和Ni具有不同的富集机制，Co热液富集作用明显。北山镁铁 超镁铁杂岩体是地幔柱相关软流圈上涌，诱发俯冲板片交代的亏损岩石圈地幔发生部分熔融，形成的高镁母岩浆演化过程中经历壳源混染、硫化物饱和富集镍钴形成铜镍钴硫化物矿床，富铁母岩浆氧逸度高、富水，岩浆分离结晶磁铁矿、叠加热液作用富集钴，形成铁钴氧化物矿床。  相似文献   

胶东海阳所超镁铁岩中强亲铁元素的地球化学特征及其构造环境探讨     

马雪盈  刘庆  闫方超  何苗  张宏远 《岩石学报》2021,37(8):2562-2578

强亲铁元素与亲石元素具有不同的地球化学行为，因此能够从不同的角度为造山带中超镁铁岩的成因及演化提供重要信息。位于苏鲁造山带东北端的胶东海阳所超镁铁岩主要由橄榄岩和辉石岩组成，它们常以团块状赋存于花岗质片麻岩中。虽然前人对这些超镁铁岩已经开展大量岩石学研究，但关于其成因及构造属性仍存在较大争议。本文开展了海阳所超镁铁岩的全岩主微量元素、强亲铁元素及Re-Os同位素的分析工作，结果显示蛇纹石化橄榄岩具有较高的MgO和Fe₂O₃^T含量，较低的Al₂O₃、TiO₂和CaO含量，明显富集流体迁移元素（U、Pb），亏损高场强元素（Zr、Hf），强亲铁元素没有发生明显分异，但Ru显示正异常，表明海阳所蛇纹石化橄榄岩是经历了低-中等程度部分熔融及熔/流体交代作用影响的残余地幔橄榄岩。海阳所辉石岩的主量元素表现出明显的结晶分异特征，稀土元素较原始地幔富集，铂族元素（PGEs）含量较低且发生了明显的分异，表明辉石岩的地幔源区经历过高程度的部分熔融和硫化物的分离。海阳所蛇纹石化橄榄岩的Os同位素地球化学特征表现出大洋亲和性，与辉石岩不具有熔体-残留体的关系。由于该地区发育较深层次的韧性剪切带，蛇纹石化橄榄岩中的橄榄石与辉石表现出韧性变形的特征，同时有辉石岩侵入到橄榄岩的现象，表明该地区的蛇纹石化地幔橄榄岩与辉石岩既不同时，也不同源，因此，暗示了该套岩石组合可能形成于大洋核杂岩（OCC）与洋脊型蛇绿岩（MOR）堆晶岩交互发育环境。  相似文献   

XANES analysis of the mechanisms of arsenic removal in biological iron and manganese treatment unit     

Yoko Fujikawa Daisuke Yoneda Atushi Minami Hiroshi Yashima Toshio Tonokai Sotoji Tani Masami Fukui Tatuhide Hamasaki Masataka Sugahara 《中国地球化学学报》2006,25(B08):113-113

Biological iron and manganese removal utilizing indigenous iron and manganese oxidizing bacteria （IRB hereafter） in groundwater can also be applied to arsenic removal according to our pilot-scale test. The arsenic removal probably occurred through sorption and complexation of arsenic to iron and manganese oxides formed by enzymic action of IRB. We investigated the chemical properties of iron and manganese oxides in IRB floc and the valence state of arsenic sorbed to the floc to clarify the mechanisms of the arsenic [especially As （Ⅲ）] removal. The floc samples were collected from two drinking water plants using IRB （Jyoyo and Yamatokoriyama, Japan）, and our pilot - scale test site where arsenic and iron removal using IRB is under way （Mukoh, Japan）. The Jyoyo and Yamatokoriyama IRB floc samples were subjected to As （Ⅲ） and As（Ⅴ） sorption experiments. The elemental composition of the floc samples was measured. XANES spectra were collected on As, Fe and Mn K-edges at synchrotron radiation facility Spring 8 （Hyogo, Japan）. FT-IR and the X-ray diffraction spectra of the samples were also obtained. The IRB floc contained ca. 35 % Fe, 0.3%-3.5% Mn and 2%-6% P. The samples were highly amorphous and contained ferrihidrites and hydrated iron phosphate. According to XANES analyses of IRB, As associated with IRB was in ＋5 valence state when As （Ⅲ） （or As （Ⅴ）） was added in laboratory sorption test, Fe in ＋3 valence state, and Mn a mixture of＋3 and ＋4 valence states. Small shift was observed in the XANES spectra of IRB on As K-edge as the equilibration time of the sorption experiment was increased. Gradual oxidation of a small amount of As （Ⅲ） associated with IRB or change in arsenic binding with sorption site were the probable mechanism.  相似文献   

胃肠酸度下中药及补铁制剂中铁活性的影响研究     

刘淑娟  王达成  杨沁羽 《华东地质学院学报》2006,29(2):159-163

在人体胃肠液的酸度条件下,采用正辛醇-水分配体系模拟药物在人体肠胃中的分配情况,研究了中药和补铁制剂中铁的形态及其在人体内的吸收情况,并探讨了中药不同比例的配伍、胃肠酸度及还原性物质的存在对水溶态铁和醇溶态铁的影响。结果表明,药物溶液中的铁形态与药物本身特性和配伍情况有关,酸度及配伍对药物中铁的溶出率和溶液中铁的形态有较大影响,人体对铁的吸收与胃肠酸度和还原性物质的存在有关。  相似文献   

Adsorption of Pentachlorophenol onto Oxide and Clay Minerals： Surface Reaction Model and Environmental Implications     

WU Daqing DIAO Guiyi YUAN Peng PENG Jinlian 《《地质学报》英文版》2006,80(2):192-199

The adsorption of pentachlorophenol （PCP） onto quartz, kaolinite, illite, montmorillonite and iron oxides has been investigated by batch equilibrium techniques. The pH-dependent isotherms are curves with peak values, the position of which is at about pH = 5-6 depending on the mineral species. Based on distribution of both speciation of surface hydroxyls on minerals and PCP in solution a surface reaction model involving surface complexation and surface electrostatic attraction is presented to fit the pH-dependent isotherms, and both reaction constants are calculated. The results show that on quartz and phyllosilicate minerals the predominant adsorption reaction is surface complexation, meanwhile both of surface electrostatic attraction and surface complexation are involved on the iron oxide minerals. The reaction constants of surface electrostatic adsorption are usually one to three orders in magnitude, larger than that of surface complexation. The concentration-dependent isotherms can be well fitted by Langmnir equation with the correlation coefficient R〉0.93 for kaolinite and iron oxides. The maximum adsorption is found in the order： hematite 〉 lepidocrocite 〉 goethite 〉 kaolinite 〉 quartz 〉 montmorillonite ≈ illite, which can be interpreted by consideration of both reaction mechanism and surface hydroxyl density. The significant adsorption of PCP onto mineral surfaces suggests that clay and iron oxide minerals will play an important role as HIOCs are adsorbed in laterite or latertoid soil, which is widespread in South China.  相似文献   

红旗岭镁铁-超镁铁岩侵入体及铜镍硫化物矿床的成岩成矿机制   总被引：7，自引：0，他引：7  

杨言辰  孙德有  马志红  许文良 《吉林大学学报(地球科学版)》2005,35(5):593-600

红旗岭铜镍矿床地处华北地台与吉黑地槽系接触带--辉发河断裂北侧.区内出露30多个镁铁-超镁铁质岩体,其中1、7号超镁铁岩体中赋存铜镍硫化物矿(床)体.含矿岩体分相明显,各类岩石均具堆积结构.铜镍矿体呈似板状、脉状、透镜状及囊状赋存于超镁铁岩体底部橄榄辉岩相中.岩石学和地球化学研究表明,7号岩体形成以流动分异为主,1号岩体为重力分异;原始岩浆属拉斑玄武质,块状矿石系压滤作用产物,后续岩浆的补给和混合补充了成矿物质,硫化物不混溶程度受挥发分制约,矿床属岩浆深部熔离分异成因,成矿时代为印支期.  相似文献   

苏鲁超高压变质带岗上石榴石橄榄岩岩体：中国大陆科学钻探卫星孔（CCSD-PP3钻孔）初步研究   总被引：7，自引：4，他引：7  

杨经绥陈世忠  张仲明许志琴吴才来  刘福来李天福陈松永  陆永增 《岩石学报》2005,21(2):293-304

大陆科学钻探在江苏岗上超镁铁岩体上打了一个卫星孔(CCSD-PP3),孔深705m,穿透428m厚超镁铁岩体,其下主要为不同类型片麻岩及少量榴辉岩。该岩体产在苏鲁超高压变质带中,面积1370×700m,上覆约10m厚第四纪盖层。岩心柱可以粗分为4段,370m上部超镁铁岩,50m片麻岩夹榴辉岩,60m下部超镁铁岩,225m片麻岩类。榴辉岩夹在片麻岩中,片麻岩有正、副之分。榴辉岩石榴石中发现柯石英假象,表明岩石经历超高压变质作用。超镁铁岩主要岩性为纯橄岩和含石榴石纯橄岩,含石榴石纯橄岩出现3层,总厚度仅90m,与不舍石榴石的纯橄岩无截然界线。岩相学研究观测到石榴石中保留橄榄石、单斜辉石和尖晶石等超高压变质之前的矿物组合,以及退变质矿物替代石榴石的现象。岩石化学成分总体变化小,SiO242.17-44.79,平均43.78;MgO46.35-48.98,平均47.42,Mg#值(=Mg/(Mg Fe)×100)为91.89-92.75,平均92.4,属于高Mg型;Al2O3和CaO丰度低,分别为0.66-0.27,平均0.43,和0,01-0.35,平均0.13;REE总量较原始地幔亏损,但LREE相对HREE富集。结合矿物组合特征,说明这套岩石属亏损型,但可能经历了流体热液的改造;纯橄岩和含石榴石纯橄岩成分的一致型,说明后者是前者经变质改造形成。SHRIMPU-Pb定年测得含石榴石纯榄岩中锆石存在两组年龄,超高压变质阶段新形成的锆石时代为240±2.7Ma,核部残留岩浆锆石给出726±56Mao前者与区域上超高压变质年龄十分吻合,后者与大别-苏鲁区域上新元古代大规模花岗质岩浆侵位时代。岗上超镁铁岩体可能记录了早期侵位到地壳,在陆陆俯冲碰撞阶段被俯冲岩片带入到柯石英形成深度,以及随岩片折返到地表的整个历史。  相似文献