氧同位素分析在东濮凹陷下第三纪沉积环境中的应用

主要介绍了氧同位素的地球化学特征，并利用这些特征在沉积环境方面的指示意义，分析了东濮凹陷下第三系盐湖沉积的氧同位素。分析结果表明：尽管保存在碳酸盐中的氧同位素的值不能定量地反映原始氧同位素的值，不能够作为区分海陆相的标志，但它可以定性地探讨碳酸盐沉积时的沉积环境。通过对东濮凹陷下第三系盐湖沉积的氧同位素分析发现，从沙四上到沙一时期，除了沙三上的δ^18O有些突变外，基本上呈递增趋势。这反映出，从沙四上到沙一时期该区的气候逐渐向干早过渡；沙四上到沙三上一段δ＾18Ｏ明显比沙一和沙二上伯低，说明在沙四上到沙三上时期，该沉积区的蒸发作用还不是很显著，而另一方面也说明在由沙三上向沙二上过渡时，该区可能存在一次气候突变，使得沙二上和沙一时期的蒸发量远大于降雨量，δ^18O的值也因此迅速增大。同时，也做了碳酸盐同位素系数Z值的研究，其揭示的沉积环境特征与氧同位素基本相同。     

马里亚纳海槽热液烟囱的显微构造及形成温度研究

本文通过对马里亚纳海槽海底热液烟囱体试样进行的扫描电镜(SEM)观测和δ18O值测定,研究了以蛋白石为主的中低温热液矿物类型和形成温度.表明纯硅质烟囱的氧同位素温度低于40℃,与黄铁矿、白铁矿和重晶石共生的热液烟囱氧同位素温度接近100℃,反映了马里亚纳海槽海底热液活动的产生条件和性质.     

渐新世/中新世分界的地层学事件

介绍渐新世/中新世分界面(即古近纪/新近纪分界面)附近的浮游有孔虫和钙质超微化石事件及其新年龄。2004年国际地层年代表确定该分界面位于第58长偏心率周期弱振幅处,古地磁事件C6Cn.2n底面,经天文调谐后的年龄为23.03 Ma。发生在该界面附近的生物地层学事件主要是浮游有孔虫Paragloborotalia kugleri的始现面(22.96 Ma)和钙质超微化石Sphenolithus delphix的末现面(23.11 Ma)。在南海北部东沙群岛附近的大洋钻探ODP1148站,渐新世/中新世界面以崩塌沉积物为特征,有明显沉积间断,标志南海当时有较大范围的构造运动。     

超过例外氧暴露时限的空气巡回潜水实验中若干生理功能的观察

17名潜水员安全地进行了55人次超过美国海军例外氧暴露时限1.5—3倍的空气巡回潜水实验。生理功能观察和肺活量测定结果表明,在水深70m以浅,潜水员均保持了相当好的智力和操作能力,在连续3d 3倍氧暴露时限的巡潜后期,只有3人肺活量下降,且在次日测定时已见恢复,表明上述暴露是安全的。美国海军例外氧暴露时限中对于70m以浅空气暴露的相应规定显得保守。     

水体势能的大气复氧法——势能增氧生态床法

天然河流水质受到污染,但水能依然存在且可以利用。研究了利用水体的势能进行大气复氧的方法,并将其引进污水生物处理领域。被污染的河水通过势能增氧生态床法进行原位生态修复后,其水质可达到地表水Ⅲ类标准,而且大大降低了污水处理费用。该研究革除了鼓风曝气进行大气复氧(利用动能),突破了污水生物处理的"障碍",充分发挥利用水体势能进行大气复氧的运行费用低的优点,开辟了水能利用的新领域。     

南海西部浮游有孔虫记录的MIS 3期表层海洋环境变化

对南海西部越南岸外上升流区17954-2站浮游有孔虫属种组合变化、浮游有孔虫氧同位素、AMS14C测年的分析以及浮游有孔虫表层海水温度、温跃层转换函数的研究结果表明:在MIS3期,南海西部表层海水温度大体呈现暖-冷-暖的变化趋势;温跃层深度由浅到深阶段性变化;短时间尺度上温度与温跃层发生幅度较大的快速变化。暖事件（IS）对应于浮游有孔虫暖水种、混合层属种含量的增加,冷水种、温跃层属种含量的减少以及冬夏SST的升高;冷事件则与之相反。表层海水生产力亦大致呈现3个阶段（61～51ka,51～42ka和42～32ka）的变化,在千年尺度的快速气候事件中,暖事件对应浮游有孔虫生产力属种含量降低,冷事件对应升高。此外,在MIS3内部分暖事件（IS6和IS11～13）表现出表层海水温度降低,温跃层深度变浅和表层海水生产力升高的状况,表明该区此时上升流的存在,其形成原因推测是由于东亚夏季风加强的结果。     

塔东地区古城4井上寒武统—中、上奥陶统流体地球化学示踪

通过对塔东地区古城4井上寒武统和中、上奥陶统碳酸盐岩围岩及充填物的碳、氧、锶同位素地球化学和流体包裹体成分的对比研究表明,充填于中、上奥陶统和上寒武统的流体分属于2个不同来源的流体体系。充填于中、上奥陶统灰岩裂缝中方解石脉的w(87Sr)/w(86Sr)介于0.7084~0.7088,它与早奥陶世海水的w(87Sr)/w(86Sr)相近;流体体系为CH4-H2O体系;充填物与围岩间具有明显的碳、氧同位素差异,表明上部流体体系中的流体来自于奥陶系地层本身。上寒武统白云岩裂缝中方解石脉的w(87Sr)/w(86Sr)为0.7138,明显地高于同时代海水的锶同位素值;流体体系为CO2-H2O体系;下部流体体系中的流体为外来富锶流体。上、下流体体系间互不连通暗示着上寒武统地层具有相对较好的保存条件。     

Carbon and oxygen isotopic composition of car- bonate cements of different phases in terrigenous siliciclastic reservoirs and significance for their origin： A case study from sandstones of the Triassic Yanchang Formation, southwestern Ordos Basin, China

Early carbonate cements in the Yanchang Formation sandstones are composed mainly of calcite with relatively heavier carbon isotope （their δ^18O values range from -0.3‰- -0.1‰） and lighter oxygen isotope （their δ^18O values range from -22.1‰- -19.5‰）. Generally, they are closely related to the direct precipitation of oversaturated calcium carbonate from alkaline lake water. This kind of cementation plays an important role in enhancing the anti-compaction ability of sandstones, preserving intragranular volume and providing the mass basis for later disso- lution caused by acidic fluid flow to produce secondary porosity. Ferriferous calcites are characterized by relatively light carbon isotope with δ^13C values ranging from -8.02‰ to -3.23‰, and lighter oxygen isotope with δ^18O values ranging from -22.9‰ to -19.7‰, which is obviously related to the decarboxylation of organic matter during the late period of early diagenesis to the early period of late diagenesis. As the mid-late diagenetic products, ferriferous cal- cites in the study area are considered as the characteristic authigenic minerals for indicating large-scaled hydrocarbon influx and migration within the clastic reservoir. The late ankerite is relatively heavy in carbon isotope with δ^13C values ranging from -1.92‰ to -0.84‰, and shows a wide range of variations in oxygen isotopic composition, with δ^18O values ranging from -20.5‰ to -12.6‰. They are believed to have nothing to do with decarboxylation, but the previously formed marine carbonate rock fragments may serve as the chief carbon source for their precipitation, and the alkaline diagenetic environment at the mid-late stage would promote this process.     

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

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     

Fe-Cu-Zn-Mo同位素示踪氧化还原过程

非传统稳定同位素（Fe-Cu-Zn-Mo）理论与数据相结合提高了科研工作者对地质体系氧化还原过程的理解。本文对这一相对较新的领域进行了综述,包括与氧化还原过程相关的同位素分馏理论和实验约束、时空尺度下的氧逸度以及同位素示踪氧化还原过程。稳定同位素理论预测,Fe-Cu-Zn-Mo同位素应该对氧化还原状态的变化能够做出响应。结果表明,Fe同位素作为岩浆过程、表生过程、俯冲带流体性质"氧逸度计"应用前景广阔;Cu同位素在岩浆、热液、陆地系统可以很好地示踪氧化还原过程;Zn同位素由于络合过程分馏已经被用在许多不同环境中作为含硫/碳流体迁移的敏感示踪剂;Mo同位素作为古氧逸度计可有效重建古海洋-大气氧化还原状态。