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1.
LING Yuan ZHENG Mianping WANG Shuxian SUN Qing XIE Bingjing ZHANG Chengjun 《《地质学报》英文版》2021,95(2):648-658
n-Alkanes are widely used in paleoenvironmental reconstructions.However,our understanding of changes in the distribution of n-alkanes with climatic and environmental factors remains unclear in arid/semi-arid regions.We sampled 26 surface sediments from three climatic zones across the southwestern Tibetan Plateau to evaluate the sensitivity of chain length distributions of n-alkanes to climatic and environmental parameters.Our observations demonstrate that average chain length (ACL), proportion of aquatic macrophyte (Paq),carbon preference index (CPI) and ratio of the contents of nC27 and nC31 (nC27/nC31) are all sensitive to hydroclimatic conditions.In contrast to commonly-adopted assumptions,the correlations between these indices and hydrological parameters are not always good,which indicates that the interpretation of n-alkane indices is special on the southwestern Tibetan Plateau.These might be related to the vegetation characteristics and seasonality of biological activity,and need to be considered in paleoclimatic reconstruction.The impact of seasonal precipitation on n-alkanes indices was also evaluated. 相似文献
2.
高海拔地区由于特殊的自然环境对气候变化和营养输入的响应十分敏感.在人类活动逐渐加强的背景下，高山湖泊高分辨率的沉积物记录了人与自然相互作用的演变过程.选取云南西北部典型高山湖泊——错恰湖，获取长度37 cm的连续湖泊沉积序列，基于铅铯测年法得到年代深度模型，并对湖芯样品进行总有机碳、总氮及正构烷烃的多指标测定和元素测量，结合气象监测数据探讨分析错恰湖的有机质来源和流域环境演化特征.根据气候代用指标的变化，两百年来错恰湖泊环境及区域气候演化可以分成4个主要阶段：1807-1900年：湖泊水位上升、湖面扩大，有机质丰度下降，有机质以外源贡献为主，内源比例上升；1900-1950年：湖泊水位开始下降、湖面收缩，有机质丰度下降，外源有机质来源增加；1950-1982年：湖泊水位下降、湖面进一步收缩，有机质丰度下降，外源输入比例继续增加；1982-2007年：湖泊水位下降、湖面收缩，有机质含量上升且以陆源输入为主，同时内源贡献比例开始增加.在元素测定结果中，人类活动对应了湖泊沉积重金属含量变化的3个阶段：1950年以前，重金属含量低且稳定，可视作自然背景阶段，人类影响忽略不计；1950年以后，湖泊流域工农业逐渐发展，人为干扰凸显；直到1982年以后，冶炼工业的进步加强了重金属的污染态势，并通过大气传输沉降被湖泊沉积物记录.错恰湖沉积记录的分析讨论在总结该区域气候环境演化历史的同时，加深了对气候人类活动湖泊生态系统相互作用过程的理解，为高山湖泊响应人类活动影响提供了证据. 相似文献
3.
对中国东北地区小兴安岭与松嫩平原过渡带五大连池青石钻孔湖相沉积物进行了有机地球化学分析,检测出丰富的正构烷烃生物标志化合物.本文主要讨论了正构烷烃的分布及其单体碳同位素组成特征.正构烷烃具有前峰型和双峰型两种分布特征,表明其有机质为混合来源,包括低等菌藻类生物和陆生高等植物输入.正构烷烃的分布特征表明,自35.2ka B.P.以来,nC27/nC31和ACL指标共同记录了东北地区小兴安岭与松嫩平原过渡带的植被以草本为主.对C27、C29和C31长链正构烷烃进行了单体碳同位素测定,并利用二元模式估算了C3和C4植物相对生物量,结果表明,自35.2ka B.P.以来,研究区的植被以C3植物为主.期间在典型冷暖气候事件中,受温度变化的影响,C3/C4植物的相对生物量有明显的变化,在全新世大暖期(6.0ka B.P.),受温度升高影响,C3植物的生物量显著减少,C4植物的生物量则明显增加;而在两次典型冷气候事件(中全新世降温事件8.2ka B.P.和新仙女木事件12.9ka B.P.)时期,受温度降低影响,C3植物的生物量有增加的趋势,C4植物的生物量则相对呈减少的趋势;在末次冰盛期21.0ka B.P.时,受明显低温特征的影响,C3植物生物量高达80.0％,这可能是当时低温的气候特征抑制了C4植物的生长.研究结果对探索我国东北地区C3/C4植物分布格局,并为评估未来气候演化对该地区植被格局和农业生产的影响提供科学依据. 相似文献
4.
The quantitative characterization of carbon isotopes of n-alkanes is commonly carried out in organic geochemical studies. Possible controls on carbon isotopes include source organic matter, maturity, fractionation during oil expulsion and migration, and the mixing of different oils. In this study of the origin of crude oils in the western Pearl River Mouth Basin, the influences of all of these factors have been considered in reaching a conclusion. Carbon isotopes of n-alkanes in the crude oils, and the extracts of the two effective source rocks (the Wenchang and Enping formations) in the basin, exhibit clear differences. The Wenchang source rocks have heavy δ13C values that remain almost constant or become slightly heavier with increasing carbon number. The Enping source rocks have light δ13C values that become lighter with increasing carbon number. Two groups of oils in this area were identified based on the carbon isotopes of the n-alkanes; groupIoils are similar to extracts of the Wenchang source rocks. However, the groupIIoils are different from both the Wenchang and Enping source rocks and the carbon isotopic profiles of their n-alkanes exhibit a “V” feature with increasing carbon number. The results of artificial thermal maturation experiments indicate that, from the early stage to the peak stage of oil generation (with EasyRo between 0.64% and 1.02%), the δ13C values of n-alkanes in the pyrolysis oils become heavier by about 3‰ with increasing thermal maturity, but the shape of the carbon isotopic profiles are not significantly changed. Calculated δ13C values of n-alkanes in “mixed” artificial pyrolysis oils indicate that the mixture of oils generated from the same source rocks with different maturities could not change the carbon isotopic profile of the n-alkanes, however, a mixing of the Wenchang and Enping oils could give the “V” feature in the profiles, similar to the groupIIoils in this area. The groupIIoils appear to be mixed Wenchang and Enping oils, the latter being the dominant component in the mixture. We conclude that the source organic matter and the degree of mixing are the main factors controlling the carbon isotopic characteristics of n-alkanes in crude oils in the western Pearl River Mouth Basin. 相似文献
5.
Two comparative simulation experiments(a normal atmospheric-pressure opening system and a 20 MPa closed system)were conducted to study the geochemical evolution of n-alkane,sterane,and terpane biomarkers in the process of oil cracking into gas under different pressures.With an initial experimental temperature set at 300°C,the temperature was increased to 650°C at a heating rate of 30°C/h.The products were tested every 50°C starting at 300°C,and a pressure of 20 MPa was achieved using a water column.The low-maturity crude oil sample was from the Paleogene system in the Dongying sag in eastern China.The threshold temperature obtained for the primary oil cracking process in both pressure systems was 450°C.Before the oil was cracked into gas,some components,including macromolecular n-alkanes,were cracked into medium-or small-sized n-alkanes.The secondary oil cracking of heavy hydrocarbon gases of C2–5to methane mainly occurred between 550°C to 650°C,and the parameters Ln(C1/C2)and Ln(C1/C3),as well as the dry coefficients,increased.Overpressure inhibited the oil cracking process.In the 20 MPa system,the oil conversion rate decreased,the temperature threshold for gas generation rose,and oil cracking was inhibited.Compared with the normal pressure system,high-carbon n-alkanes and other compounds in the 20 MPa pressure system were reserved.Furthermore,the parameters∑C21-/∑22+,Ln(C1/C2),and Ln(C1/C3),as well as the dry coefficients,decreased within the main temperature range.During secondary oil cracking(550°C to 600°C),the Ph/nC18and Pr/nC17decreased.High pressure influenced the evolution of the biomarkers Ts and Tm,C31homohopane,C29sterane,and their related maturity parameters to different extents during oil cracking under different temperature ranges. 相似文献
6.
通过自然条件下沙表层和水面溢油的模拟风化实验,采用GC-MS作为检测器,研究原油中的正构烷烃在厦门地区的风化规律.结果表明,在一个月的风化模拟实验中,两种不同介质溢油风化均明显体现轻组分的正构烷烃丢失现象,且正构烷烃组分在水面溢油的风化速率低于沙表层溢油速率1～2个碳数.沙上模拟实验后期APr/APh比值明显受到风化影响,诊断比值不适用于油源鉴别.诊断比值An-C17/APr、An-C18/APh在短期风化过程中受风化影响小.水面溢油模拟实验结束后发现水体中n-C13-n-C29的正构烷烃组分含量升高2.9%～327.4%. 相似文献
7.
广州市空气颗粒物中烃类物质的粒径分布 总被引：13，自引：1，他引：12
用 Andersen六段分级大流量采样器 (粒径为 : 10～ 7.2 μ m, 7.2～ 3.0 μ m, 3.0～ 1.5 μ m, 1.5～ 0.95 μ m, 0.95～ 0.49 μ m, ≤ 0.49 μ m)采集了广州市荔湾区 4个季度的大气颗粒物样品 , 用气相色谱 (GC)定量分析了其中的正构烷烃 (n-alkanes)组分,用气相色谱-质谱 (GC-MS)定量分析了其中的多环芳烃 (PAHs)组分. CPI2(代表石油成因的碳优势指数 )、 CPI3(代表生物成因的碳优势指数 ) 和 Wax(植物蜡含量 )表明了石油成因的烷烃倾向于富集在细颗粒物上,而生物成因的烷烃倾向于富集在粗颗粒物上.正构烷烃和低相对分子质量多环芳烃表现出双峰模型分布,高相对分子质量多环芳烃呈现单峰模型分布,仅在细颗粒段有一峰值.烷烃和芳烃秋冬季的 MMDs(质量中值直径 )比春夏季的大.在高温季节化合物优先富集在细颗粒物上,而在低温季节则向粗的颗粒物方向偏移. 相似文献
8.
南海现代沉积物中正构烷烃碳分子组合特征及其指示意义 总被引：5，自引：0，他引：5
利用1998年6~9月南海海洋环境调查及1987年SO-50中德联合调查中所取得的资料,对南海沉积物中正构烷烃碳分子组合特征进行分析和研究,并将南海与渤海、黄海、东海现代沉积过程中的正构烷烃碳分子组合特征进行对比,结果表明:(1)南海北部沉积物中正构烷烃碳分子分布范围为nC15~nC33,双峰群,居前的低碳数主峰碳为nC19~nC22,居后的高碳数主峰碳为nC27,nC24以后奇碳的优势明显,OEP为2.13,nC23-/nC24 值平均为1.53,沉积物中陆源输入居多;南海南部沉积物中正构烷烃碳分子分布范围为nC15~nC33,呈双峰群,居前的低碳数峰群以nC19~nC23为主峰碳,居后的高碳数峰群以nC27或nC29为主峰碳,OEP为1.58,nC23-/nC24 值平均为2.15,沉积物中海洋生物来源居多。南海沉积物中正构烷烃碳分子为海洋和陆源两种有机质来源。(2)南海南部处于典型热带海洋环境,生物生产力较高,大量硅质、钙质生物在海域繁殖,生物效应降低了陆源物质的丰度。物源效应和生物效应的差异是南海南、北部现代沉积物的碳分子组合分布变化的主要原因。(3)南海现代沉积物各站位沉积物中正构烷烃的P r/Ph值基本小于1,说明沉积物沉积时为缺氧还原的沉积环境,但局部海域沉积环境具有较强的氧化性,沉积物在沉积过程中一定程度上受到涌升的南极底层水的影响。(4)南海与东海、黄海、渤海不同海域沉积物中正构烷烃碳分子组合特征对比可知,各海域沉积物均显示出物源效应。 相似文献
9.
植物正构烷烃及其单体氢同位素在古环境研究中的应用 总被引：5，自引：1，他引：4
正构烷烃是植物类脂的重要组成部分,主要用来维持叶片表面的水分平衡,其平均碳链长度(ACL)作为植物对水分胁迫程度的生理性反映,与植物进化程度存在表观上的联系。高等植物来源烷烃的ACL高于低等植物和水生藻类,裸子植物高于被子植物,C4植物高于C3植物,因此植物正构烷烃具备粗略的植物分类学意义,并在古环境研究中被广泛应用。在河口和海洋沉积物中主要用来判断水生低等植物和陆地高等植物的相对贡献,在古土壤中则用来区分草本/木本植物的消长变化。植物烷烃中的氢元素主要来自光合作用时吸收的环境水,其δD主要受环境条件和生物化学过程影响,但环境条件、气候状况和植被类型的影响可以在很大程度上相互抵消,使烷烃δD具有记录大气降水δD的潜力,从而可以用来重建大气降水δD并反演气候变化。 相似文献
10.
Hydrogen isotope of individual n-alkanes from modern sediments and their application to environments
Zhongping LI Liwu LI Li DU 《中国地球化学学报》2006,25(B08):207-207
Hydrogen isotopes are commonly fractionated to a much greater extent and as a result display larger variations in δ values, In terms of the hydrogen isotope ratios of individual n-alkanes of 16 samples of modern sediments selected from four different locations in the southern part of Gansu, China, the δD values for most of the n-alkanes varied from -150‰-300‰, Variations in δD also occurred between different ranges of n-alkanes, effects of environmental changes on the hydrogen isotopic compositions of individual n-alkanes have been detected. Besides the δD values of n-alkanes, the δD values of lipids including pristane （Pr）, phytane （Ph） were also examined, by the combination of D/H ratios with molecular fingerprinting, Our results further support the notion that hydrogen isotopes of n-alkanes from modern sediments can act as paleoclimatic and paleoenvironmental proxies and provide invaluable new sources of information in the research of paleoenvironment reconstruction. 相似文献