Molecular and isotopic compositions of bitumens in Silurian tar sands from the Tarim Basin,NW China: Characterizing biodegradation and hydrocarbon charging in an old composite basin

Biodegradation and oil mixing in Silurian sandstone reservoirs of the Tarim Basin, one of the largest composite basins in China, were investigated by analyzing the molecular characteristics and stable carbon isotopic signatures of low-molecular-weight (LMW) saturated hydrocarbons and high-molecular-weight (HMW) asphaltenes. Detection of 25-norhopanes and 17-nortricyclic terpanes in most Silurian tar sands from the Tabei Uplift in the Tarim Basin suggests a much greater degree of biodegradation here than in the Tazhong Uplift. This explains the relatively more abundant tricyclic terpanes, gammacerane, pregnane and diasteranes in tar sands from the Tabei Uplift than in those from the Tazhong Uplift. Hence, care must be taken when assigning oil source correlations using biomarkers in tar sands because of the biodegradation and mixing of oils derived from multiple sources in such an old composite basin. Asphaltenes in the tar sands seem to be part of the oil charge before biodegradation, depending on the relative anti-biodegradation characteristics of asphaltenes, the similarity in carbon isotopic signatures for asphaltenes and their pyrolysates, and the consistent product distribution for flash pyrolysis and for regular steranes in asphaltene pyrolysates, regardless of whether the tar sands were charged with fresh oil. According to the relative distributions of regular steranes and the relatively abundant 1,2,3,4-tetramethylbenzene significantly enriched in ¹³C, the oil sources for asphaltenes in the tar sands might be related to lower Paleozoic marine source rocks formed in euxinic conditions. Nevertheless, the relatively low abundance of gammacerane and C₂₈ regular steranes observed in asphaltene pyrolysates and residual hydrocarbons, within limited samples investigated in this work, made a direct correlation of oils originally charged into Silurian tar sands with those Cambrian source rocks, reported so far, seem not to be possible. Comparison of carbon isotopic signatures of n-alkanes in asphaltene pyrolysates with those of LMW saturated hydrocarbons is helpful in determining if the abundant n-alkanes in tar sands are derived from fresh oil charges after biodegradation. The limited carbon isotopic data for n-alkanes in LMW saturated hydrocarbons from the tar sands can be used to classify oils charged after biodegradation in the composite basin into four distinct groups.     

Effect of atmospheric CO2 and solar activity on wind regime and water column stability in the major global upwelling areas

It is not clear whether global warming will favour or reduce global ocean phytoplankton productivity in coastal areas. Moreover, the relative contributions made by natural and/or anthropogenic factors to possible changes in phytoplankton productivity are not clear. As the relationship between primary production and alongshore wind forcing is well established for the Eastern Boundary Current (EBC) ecosystems, our aim is to determine whether the changes experienced over the last five decades (1958–2007) in atmospheric CO₂ and solar activity have been able to affect the wind regime and water column stability in the most biologically productive upwelling areas of California, Canary, Humboldt and Benguela. We approached the work by statistically studying the effect of solar activity and atmospheric CO₂ on surface alongshore wind stress and on water column stability. There was an increasing trend in wind stress and water column stability in all the upwelling areas over the period studied (with the single exception of stability in the California EBC system). The analysis of detrended series evidenced significant relationships between atmospheric CO₂ concentration and wind stress and water column stability in the coastal upwelling areas investigated. In addition, wind stress and stability data were found to be consistent, with negative linear relationships between wind stress and CO₂ in most of the sites in the Benguela, Canary and Humboldt regions associated, as expected, to positive relationships when water column stability is used as regressand. The results of the present study suggest that greenhouse gas forcing, independent of its well known general increasing trend, was able to decrease wind stress intensity and increase water column stability for the period 1958 to present in most of the sites of the four Eastern Boundary Ecosystems studied, with the one exception of the California region. Conversely, the impact of solar activity appeared to be quite low compared to the greenhouse gas forcing.     

深海热液区主要成分的高温高压拉曼光谱分析

模拟深海热液口环境(最高压力40 MPa,最高温度350℃),对深海热液区的主要成分CO2、CH4及其混合物的水溶液在不同压力和温度条件下的拉曼光谱进行探测和分析,结果显示:常温低压下CO2水溶液的Fermi双峰分别位于1 384.9 cm-1和1 278.3 cm-1处,CH4的水溶液拉曼峰υ1位于2 912.1 cm-1处,均比其气相的拉曼频移小;常温下CO2和CH4水溶液的拉曼特征峰随压力(≤40 MPa)的变化均不明显;在40 MPa的压力下随着温度的升高(≤350℃),CO2水溶液的Fermi双峰分别向高波数区移动了约3.4 cm-1和7.0 cm-1,而CH4水溶液的拉曼峰υ1向低波数区移动了约3.1cm-1;混合后升温过程中CO2的双峰分别向高波数区移动了约4.3 cm-1和3.8 cm-1,CH4的特征峰υ1向低波数区移动了4.5 cm-1。说明在室温到350℃范围内温度的变化对CO2和CH4水溶液拉曼频移有影响,频移量与温度线性相关,而压力在≤40 MPa范围内的改变对拉曼频移影响不明显。     

碳市场与电力市场机制影响下发电机组成本分析与竞争力研究

碳市场和电力市场将共同发挥市场对资源优化配置的决定性作用,对共同市场主体发电企业带来经营和发展挑战.在考虑碳成本的基础上,采用发电机组经济性影响模型,定量分析了碳市场不同发展阶段对发电机组发电成本的影响,定量评价不同能源结构投资收益经济性,以及对集中竞价市场出清顺序的影响.结果表明,随着有偿配额比例和碳价增加,碳成本占...     

盘锦湿地芦苇生态系统长期通量观测研究

针对2004年5月26日-2005年10月15日盘锦湿地芦苇生态系统碳通量、感热通量和潜热通量资料进行分析。结果表明:芦苇湿地具有较强的碳汇作用;2005年芦苇湿地固定二氧化碳为13.32 t/hm2,日平均感热通量和潜热通量分别为2 464 kJ/m2和3 880 kJ/m2。2004年和2005年6～9月的日累积值波文比平均值均为0.15。芦苇湿地碳通量、感热通量和潜热通量的日动态呈单峰单谷型变化,极值出现在中午前后,夜间线形平直。芦苇生长季白天通量绝对值远较夜间大,白天碳吸收,夜间碳排放。CO2浓度年平均日变化曲线亦为单谷单峰型,夜间浓度较高且逐渐升高,直到日出前达到峰值;日出后急剧下降,傍晚又开始逐渐增加。芦苇湿地感热通量昼正夜负,潜热通量与林地不同,全天为正。各通量季节变化明显,冬季CO2通量日变化不明显,趋近于零;感热通量总体向上输送,春季数值较大,生长季数值较小;潜热通量冬季最小,接近0,春季开始显著增加,生长季达到最大。     

The influence of medium-range transport on O3 levels at a rural site in Israel

Simultaneous ozone measurements were made at a rural site, 25 km SSW of the city of Jerusalem, and in the center of the city during a period of 28 months. The ozone data were supplemented by SO₂, NO/NO _x ,and meteorological measurements at both sites. Elevated ozone concentrations were recorded at the rural site, mostly during the spring months (May and June) during which the monthly averages and the monthly averages of the daily 30 min maximum levels equalled those measured in the city. During the summer months, both average and peak levels were lower at the rural site by 20 and 35 ppb. The increased ozone levels at the rural site were accompanied by a parallel increase of SO₂ and NO _x ,suggesting hat the excess ozone at the rural site is a result of a transformation during transport of air pollutants from coastal sources.     

On the significance of CO2 inclusions in plagioclase microphenocrysts in tholeiite from Moeraki,New Zealand

Liquid plus vapour inclusions of CO₂ are widespread in plagioclase microphenocrysts in small tholeiitic intrusions and tephra of the Moeraki and adjacent areas of northeast Otago, New Zealand. They imply the presence of immiscible CO₂ droplets in the magma at depths of about 7–14 km. Their presence within 5 μm of the edges of microphenocrysts as little as 35 μm thick and 118 μm long indicates minimal feldspar crystal growth during the final ascent and quenching of the magma. Delicate branching clusters of lath-like microphenocrysts escaped disruption during this ascent. Such CO₂ inclusions are a potential source of ‘excess argon’ perturbing K-Ar age determinations. Received March 24, 1993/Accepted September 10, 1993     

单柱离子色谱测定二氧化锰产品中无机阴离子杂质

采用了单柱离子色谱法测ＭｎＯ２产品中无机离子杂质；提出了消除干扰的可行途径，将Ｌａ（ＯＨ）３加入后能同时消除进样峰的干扰和溶剂峰的出现。选用１．７５ｍｍｏｌ／Ｌ邻苯二甲酸１．７５ｍｍｏｌ／Ｌ三羟甲基氨基甲烷为混合淋洗剂测定Ｆ＾－，Ｃｌ＾－，ＮＯ３＾和ＳＯ＾２－４，其标准加入回收率为９５％－１０５％；ＲＳＤ（ｎ＝７）为２．４７％－８．０８％。     

The biogeochemical sulfur cycle in the marine boundary layer over the Northeast Pacific Ocean

The major components of the marine boundary layer biogeochemical sulfur cycle were measured simultaneously onshore and off the coast of Washington State, U.S.A. during May 1987. Seawater dimethylsulfide (DMS) concentrations on the continental shelf were strongly influenced by coastal upwelling. Concentration further offshore were typical of summer values (2.2 nmol/L) at this latitude. Although seawater DMS concentrations were high on the biologically productive continental shelf (2–12 nmol/L), this region had no measurable effect on atmospheric DMS concentrations. Atmospheric DMS concentrations (0.1–12 nmol/m³), however, were extremely dependent upon wind speed and boundary layer height. Although there appeared to be an appreciable input of non-sea-salt sulfate to the marine boundary layer from the free troposphere, the local flux of DMS from the ocean to the atmosphere was sufficient to balance the remainder of the sulfur budget.