Fluid sources and stable isotope signatures in authigenic carbonates from the Northern Apennines,Italy     

《Marine and Petroleum Geology》2017

Authigenic carbonates are frequently associated with methane cold-seep systems, which extensively occur in various geologic settings worldwide. Of interest is the relation between the fluids involved in their formation and the isotopic signals recorded in the carbonate cements. Along the Northern Apennines foothills (Italy), hydrocarbons and connate waters still seeping nowadays are believed to be the primary sources for the formation of fossil authigenic carbonate found in Plio-Pleistocene marine sediments. Four selected outcrops of dolomitic authigenic carbonates were analysed to compare signature of seeping fluids with fractionation of stable carbon and oxygen isotopes recorded in the carbonate.Along the foothills, deep methane-rich fluids spontaneously rise to the surface through mud volcanoes or are exploited in wells drilled nearby to the fossil Plio-Pleistocene authigenic carbonates. The plumbing system providing fluids to present-day cold seeps was structurally achieved in Late Miocene and Plio-Pleistocene. δ¹³C values of methane, which vary from −51.9 to −43.0‰ VPDB, indicate that gas composition from the deep hydrocarbon reservoirs is relatively uniform along the foothills. On the contrary, δ¹³C in fossil authigenic carbonates strongly varies among different areas and also within the same outcrop.The different carbon sources that fed the investigated carbonates were identified and include: thermogenic methane from the deep Miocene reservoirs, ¹³C-enriched CO₂ derived from secondary methanogenesis and microbial methane from Pliocene successions buried in the Po Plain. The δ¹³C variability documented among samples from a single outcrop testifies that the authigenic carbonates might represent a record of varying biogeochemical processes in the hydrocarbon reservoirs. The sources of stable oxygen isotopes in authigenic carbonates are often ascribed to marine water. Oxygen isotopic fractionation in the dolomite cements indicates that marine pore water couldn't be the sole source of oxygen. δ¹⁸O values provide a preliminary evidence that connate waters had a role in the carbonates precipitation. The concomitant occurrence of active cold seepages and fossil record of former plumbing systems suggests that generation and migration of hydrocarbons are long-lasting and very effective processes along the Northern Apennines foothills.  相似文献   

湖泊碳酸盐在过去环境变化研究中的应用   总被引：2，自引：0，他引：2       下载免费PDF全文

郭金春  马海州  宋恩玉  陈宁 《盐湖研究》2008,16(2):66-72

国内外的研究成果表明,湖泊沉积碳酸盐矿物及其微量元素、同位素分布特征记录了全球或区域古气候环境演变历史,可以从中提取大量定量化的古气候参数。因此,可以根据湖泊碳酸盐矿物的含量和碳、氧同位素变化等信息推知其形成时期的气候环境,重建古环境,揭示气候环境演变的规律。湖泊碳酸盐是一种研究古环境演化重要的代用指标,在过去气候环境变化研究中有广阔的应用前景。  相似文献   

Improvement of Oxygen Release from Calcium Peroxide‐polyvinyl Alcohol Beads by Adding Low‐cost Bamboo Biochar and Its Application in Bioremediation          下载免费PDF全文

Chih‐Hung Wu  Shih‐Hsien Chang  Chi‐Wen Lin 《洁净——土壤、空气、水》2015,43(2):287-295

  相似文献   

Paramagnetic lattice defects in quartz for applications to ESR dating     

《Quaternary Geochronology》2015

Quartz is one of the minerals useful for ESR dating with many applications. Although the study has quite a long history since 1980's, ESR dating of quartz is still in a developing stage. After the basis in physics for the ESR signals in quartz is described, the current status of ESR dating of quartz is summarized for applications to fault gouge, tephra and sediment. Both basic studies for mechanisms and practical applications with independent age controls are still necessary to establish the protocols.  相似文献   

大荔人遗址黄土-古土壤剖面岩石磁学性质研究   总被引：1，自引：0，他引：1       下载免费PDF全文

霍俊杰  Reidar Lovlie  李斌  苏朴 《地球物理学报》2010,53(6):1463-1474

自从大荔人化石被发现以来,其遗址剖面便成为研究热点.先前的研究主要集中在地层的对比划分与头盖骨年龄的推断方面,然而对于载磁矿物的鉴定及其古气候含义方面的研究却相对较少.鉴于此,本文运用热磁分析、饱和等温剩磁和剩磁矫顽力谱分析、磁滞回线分析、频率磁化率分析、热退磁分析等方法,对大荔人遗址剖面进行了系统的岩石磁学性质研究,鉴定出其主要载磁矿物为磁铁矿,赤铁矿,磁赤铁矿,磁畴状态主要是似单畴.磁铁矿,赤铁矿是样品中特征剩磁的携带者;主要起源于成土作用的超顺磁颗粒和新生成的亚铁磁性矿物,是古土壤样品磁化率增强的主要贡献者;古土壤中软磁性矿物的含量高于黄土.样品中磁赤铁矿的含量并不高.黄土-古土壤样品的频率磁化率曲线,古里雅冰芯氧同位素、细微粒浓度曲线,岐山五里铺剖面有机质含量曲线在古气候记录方面具有一致性,都展示出至少从MIS5以来,气候从冰期到间冰期的变化是渐变的,反之则表现了突变特征.上述岩石磁学研究丰富了大荔剖面的磁学领域研究内容,为相关课题的深入研究提供了依据.  相似文献   

Local variability of sedimentation rate in Lake Arendsee, Germany     

Burkhard W. Scharf  Bertram Boehrer  Conrad Kopsch 《Limnologica》2010,40(2):97-101

We measured the thickness and the dry weight of recently deposited sediment along several transects across Lake Arendsee in order to quantify the sedimentation rate and its local variability. As a time marker, we used an artificial marl layer that was deposited by a remediation program in the year 1995. A portion of the sediment deposited during the year was transported from the littoral and the top of the submerged hills to the foot of the slope, where we found the greatest deposition. Within the same lake, the deposited sediment layer varied by a factor of 4 between minimal and maximal values over the same time periods. Lake Arendsee is a holomictic and eutrophic lake with depletion of oxygen in summer time.  相似文献   

湖泊无机碳酸盐矿物氧同位素组成差值及其单矿物同位素组成的确定          下载免费PDF全文

曾承  吴鑫  钱晨阳 《盐湖研究》2010,18(1):21-28

湖积物中不同无机碳酸盐矿物常常混杂在一起,其氧同位素组成(δ18O)差异会影响碳酸盐δ18O环境信息提取的可靠性。不同矿物之间δ18O差值明显且幅度不一。20~25℃时生成的白云石比共生的方解石富集18O可能为0‰~9‰不等,亦或方解石比白云石可能更富集18O达0‰~12.3‰。常温状态,相同条件下形成的文石δ18O值较方解石高出0‰~1‰,或者方解石较文石δ18O值高出0‰~4.47‰。镁方解石中MgCO3的mol百分含量每增加1%,其δ18O值相对于纯方解石δ18O值增加0.06‰~0.17‰。在利用碳酸盐δ18O进行气候及环境研究时,不能根据某种差值进行校正,而应进行单矿物测试。由此,对不同无机碳酸盐矿物的分离及同位素测试、推算方法进行了归纳和述评。  相似文献   

Separation of Vanillin and Syringaldehyde from Oxygen Delignification Spent Liquor by Macroporous Resin Adsorption     

Zhaojiang Wang  Kefu Chen  Jun Li  Qianqian Wang  Jie Guo 《洁净——土壤、空气、水》2010,38(11):1074-1079

This paper reports on an approach for separating vanillin and syringaldehyde (VSA) from oxygen delignification spent liquor using non‐polar macroporous resin. The effects of temperature and pH on the adsorption isotherms were studied. The adsorption capacity and adsorption equilibrium constant were obtained using the Langmuir adsorption model at pH<4.5, where the ionization of the VSA to ionic forms was negligible. The standard enthalpy change was calculated using the van't Hoff equation and clearly showed that the adsorption is an exothermic process. The effect of pH on the adsorption isotherm is well‐described by a modified Langmuir model and shows that the adsorption equilibrium constant decreases significantly with the increasing pH. The VSA adsorbed on macroporous resin was eluted by ethyl ether. The separated VSA contained 37.51% vanillin, 31.88% syringaldehyde. The recoveries of VSA were 96.2 and 94.7%, respectively.  相似文献   

Using ocean quahog (<Emphasis Type="Italic">Arctica islandica</Emphasis>) shells to reconstruct palaeoenvironment in Öresund,Kattegat and Skagerrak,Sweden     

Elena Dunca  Harry Mutvei  Peter Göransson  Carl-Magnus Mörth  Bernd R. Schöne  Martin J. Whitehouse  Mikael Elfman  Susanne P. Baden 《International Journal of Earth Sciences》2009,98(1):3-17

Shells of Arctica islandica collected between 1884 and 2004 from Öresund, Kattegat and Skagerrak (Swedish West Coast) were used to monitor local climate variations and the influence of human activities on the local environment. For this purpose, we analysed the growth, structure and chemical composition of these shells and compared them with shells collected from Kiel Bay, Norway and Iceland. The growth rate of the studied shells registers an NAO periodicity of ca 8 years. However, the observed signal is weak because of other environmental interferences that are either of natural or anthropogenic origin. For example, the oxygen isotope ratios show temperature fluctuation, but also the influx of low salinity water. Higher contents of S, N, Cu, Zn, As, Cd and P in shell portions formed during the last century are related to human activities such as mining and industrial development. Our study indicates that in order to use Arctica shells as archives of climate change it is necessary to study the full range of environmental data that is recorded in the shells by using a multi element and isotope approach in combination with different analytical techniques including investigation of growth rates and shell structure.  相似文献   

Comparison of an Electrochemical and Luminescence‐Based Oxygen Measuring System for Use in the Biodegradability Testing According to Closed Bottle Test (OECD 301D)     

Judith Friedrich  Andreas Längin  Klaus Kümmerer 《洁净——土壤、空气、水》2013,41(3):251-257

The effects of persistent organic pollutants on the aquatic environment still can hardly be assessed. Therefore, ready biodegradability is a desired key characteristic of chemicals. Accordingly, biodegradation testing is of utmost importance and is a vital part within the risk assessment for organic chemicals. In the closed bottle test (CBT; OECD 301D) the degree of biological degradation of a chemical is assessed by monitoring the oxygen consumption so far with a Clark electrode as standard method. However, this method is time‐consuming, laborious and led to frequent fluctuations of the test results, which limited their validity. Due to these shortcomings, an optical system that enables contact‐free measuring of the oxygen concentration in a closed bottle, based on dynamic luminescence quenching, was examined. The test results were compared to those obtained with the “classical” electrochemical technique (Clark electrode). At first, a basic standard for the handling of the new instrument in the laboratory was developed. Then possible influencing factors, reliability, comparability, and reproducibility of the test results were investigated by running the CBTs in parallel with the electrode and optode method. The findings proved the new optode method to be unambiguously superior to the electrode technique. The frequency of fluctuations of the test results and time and effort necessary for the test run could considerably be reduced. The degradation kinetics of the test substances could be followed easily in the CBT by increasing the measuring points without much additional effort.  相似文献