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1.
应用水中有机组分包括酚、苯、溶解烃气、紫外吸收光谱和荧光光谱测试的烃以及δ13℃1进行的化探测量,在测区发现I级异常1个,Ⅱ级异常4个,Ⅲ级异常3个,为油气勘探提供了具体部位;同时还发现了钾的高值异常带,且勘探证明在深层地下水中K+的含量可达5791.5ppm。因此为油气与钾盐兼探指出了有利地段。  相似文献   

2.
植物化石和土壤中的有机质碳同位素指标常用来反映古气候的变化,然而碳同位素这个指标在特定地区反映气候的定量关系缺乏检验。研究剖面选择自中国的秦岭(34°14'24″N,106°55'30″E)到蒙古人民共和国北部,接近贝加尔湖地区(51°35'08″N, 100°45'49″E)的研究剖面线,选择了3种C3植物(Artemisia scoparia, Ajania achilleides 和 Artemisia frigida),在剖面线上沿南北方向上每隔4'到5'采取一个样点,共选取161个C3植物茎叶样品进行了δ13 C值测定。同时收集了剖面线附近气象站的降水、气温等资料,用插值方法得到每个采样点的气温、降水数据。分析表明:C3植物的δ13 C值分布范围为-30 ‰ ~-22 ‰ ,其平均值为-26.81 ‰ ,该平均值较全球C3植物δ13 C平均值偏正。通过对比C3植物δ13 C与年均温、年均降水量、生长季节的干燥度等随纬度的变化规律,发现C3植物δ13 C、年均降水量、生长季节的干燥度有非常一致的变化趋势,而C3植物δ13 C和年均温不具有一致性。通过一元回归分析也同样发现C3植物δ13 C与年均降水量呈线性负相关关系(y=-0.0077x-24.838,n=161,R2=0.4418,p=0.01),与生长季节的干燥度呈线性正相关关系(y=0.7328x-28.806,n=161,R2=0.3685,p=0.01),而与年均温度没有明显的相关关系(y=-0.0461x-26.756,n=161,R2=0.0232,p=0.01)。在本研究区C3植物δ13 C对年均降水量和生长季节的干燥度响应十分显著,而对温度的响应不明显。研究区具有明显的降水和温度的梯度分布特征,是验证植物碳同位素与气候关系的理想场所,而土壤中的有机质碳同位素与其地面上的植物碳同位素息息相关。研究也说明,在本研究区或其他气候植物组合相似的地区可以利用古土壤中的有机质碳同位素来定量或半定量地反映古气候的变化。  相似文献   

3.
为了揭示蜗牛化石壳体碳酸盐（文石）稳定同位素组成的古气候和古生态环境指示意义,对采集于河南荥阳邙山末次冰期黄土剖面上部中的粉华蜗牛（Cathaica pulveratrix）化石壳体碳酸盐进行了碳、氧稳定同位素分析,同时还对全岩有机物质（SOM）碳同位素组成以及全岩磁化率和粒度等气候替代指标进行分析,结果显示：剖面中反映蜗牛食物碳同位素组成的壳体δ13CSSA的变化,与反映古植被碳同位素组成的全岩有机物质碳同位素组成（δ13CSOM）无显著的相关关系,但是壳体13C相对于SOM的富集程度（Δδ13CSSA-SOM）的变化与石笋氧同位素记录的末次冰期东亚夏季风强度演化同步一致;   壳体δ18OSSA的变化不但与黄土磁化率、粒度等气候替代指标变化具有显著相关性,同样也与末次冰期东亚夏季风强度演化同步一致。这些特征,一方面说明受季风环流控制的气候温湿程度变化左右蜗牛夏季活动的几率和食物的类型,干冷气候条件下,相对温湿夏季成为蜗牛活动主要时期,相对富集13C苔藓、菌类和植物可能是蜗牛的主要食物;   另一方面暗示蜗牛化石壳体碳酸盐稳定同位素组成能够指示气候温湿程度和生态环境的变化。  相似文献   

4.
结合含水量、TOC含量和TOC/TN比值变化曲线,18·5kaB·P·以来的四海龙湾玛珥湖沉积物全岩有机碳同位素组成（δ13CTOC）记录可划分为3个阶段:1)末次冰期晚期（18·5～14·7kaB·P·）,δ13CTOC值偏正,变化范围为-29·50‰～-26·18‰,平均值约为-28·10‰;2)末次冰消期（14·7～11·7kaB·P·）,δ13CTOC值显著偏负,变化范围为-33·92‰～-28·40‰,平均值约为-31·75‰,在δ13CTOC值变化曲线上表现为一个低谷,但在类似YoungerDryas的冷干事件期间（12·7～11·7kaB·P·）,δ13CTOC值再次显著偏正,最高可达-28·4‰;3)全新世以来（11·7kaB·P.至今）,δ13CTOC值变化幅度不大（-30·85‰～-27·37‰）,基本上都在平均值-29·1‰左右。研究表明,大气CO2浓度变化是影响18·5kaB·P·以来四海龙湾玛珥湖δ13CTOC值变化的主导因素。  相似文献   

5.
甲烷稳定碳同位素组成（δ^13C1）作为气态烃的示踪剂,是近地表油气化探中常用的判别烃类来源的方法。油气化探中分析土壤中不同赋存状态的烃类的甲烷稳定碳同位素,一直沿用有机地球化学中的标准来确定地表土壤中的烃类属何种成因,所获得的结果往往令人难以信服。通过对已知区近地表土壤不同赋存状态烃类的甲烷碳同位素特征分析,认为由于分馏现象、成壤母岩、运移机制等,近地表化探烃类异常的甲烷碳同位素有其自身的特点,在应用时应考虑甲烷碳同位素比值的干扰因素,从而把地表痕量轻烃稳定碳同位素与地下深部油气建立相应的联系,反映真假异常,提高油气化探异常的可信度。  相似文献   

6.
藏北双湖县巴岭乡地区出露一套深水相黑色页岩地层,包括下侏罗统曲色组和中侏罗统色哇组二个组地层单元。根据菊石化石控制的生物地层时代,下伏曲色组划归Pliensbachian-Toarcian 阶,上覆色哇组级代表Aalenian-Bajocian 期沉积,二者之间为连续沉积,是目前西藏特提斯域菊石化石控制程度最高的中下侏罗统地层。野外实测了索布查J2/J1界线剖面,按2m间距采集了148件样品,室内开展了无机碳(δ13Ccarb)和有机碳(δ13Ckero)分析,目的是揭示早侏罗世末期到中侏罗世初期这一时段的古海洋演化过程。研究结果表明,曲色组沉积期古海水δ13CDIC偏正,而色哇组δ13CDIC偏负,J2/J1界线上下δ13Ccarb值显示阶步式负向偏移的特点。根据相关分馏方程计算,Toarcian期海洋浮游植物繁盛,δ13CDIC偏正,海水营养盐NO3浓度偏低,而Aalenian期海洋浮游植物衰减,δ13CDIC偏低,NO3浓度升高。沉积有机质或干酪根碳同位素δ13Ckero在J2/J1界线上下与δ13Ccarb变化趋势一致,也具有由高值逐渐偏低的特点,但δ13Ccarb和δ13Ckero变化曲线的波峰和波谷并不同步,这是因为海源和陆源有机质相对含量高低变化所致。文中根据碳同位素质量平衡方程,定量的描述了索布查界线剖面陆源和海源有机质比例的变化过程,讨论了曲色组和色哇组烃源岩在油气勘探中的意义。  相似文献   

7.
通过对中国西北干旱区石羊河流域民勤盆地三角城古湖泊沉积物有机质碳同位素组成(δ13Corg)分析,表明末次冰期与全新世时气候和植被有明显的差异,末次冰期δ13Corg总体偏轻(-30‰～-25‰),而全新世碳同位素组成则有较大的变化,在早全新世碳同位素组成有多次短期快速变重(-10‰左右)的变化,中全新世碳同位素组成总体偏重(-20‰～-10‰),晚全新世碳同位素组成偏轻(-25‰左右)。分析表明湖泊沉积物有机质碳同位素组成反映了陆生C3植物和湖泊内源水生植物变化的关系,末次冰期以来西北干旱区C4植物不发育,偏重的有机质碳同位素值与C4植物无关。从沉积物中有机质组分、元素等分析表明,末次冰期时主要以河流相沉积为主,湖泊中有机质主要来源于上游祁连山的陆生C3植物,有机碳含量较低,表明当时的上游的陆生植被不繁盛,区域气候较干冷;从全新世开始,三角城古湖泊开始形成,沉积物中碳同位素组成偏重的有机质主要来源于湖泊中的沉水植物,此时湖泊水体较大,湖泊生产力较高。而沉积物中有机质碳同位素组成偏轻时期的有机质主要来源于挺水植物、陆生C3植物,较低的有机碳含量说明该时期陆生植被不发育,气候较干冷,湖泊水体较小  相似文献   

8.
鄂尔多斯盆地上、下古生界地层包裹体气体与气藏中气体地球化学性质对比表明:上古生界气藏中气体与包裹体中气体地球化学性质相似,气藏中气体的地球化学性质能代表成藏初期气体的原始特征;而下古生界气藏中气体与包裹体中气体的地球化学性质差别很大,下古生界气藏中的气体与下古生界源岩模拟生成气体也有非常大的差别。因此,下古生界气藏中的气体不能代表来自下古生界源岩产生天然气。结合前人关于奥陶系源岩的模拟生成天然气、包裹体中气体以及靖边气田天然气的地球化学特征,提出来源于奥陶系的天然气应具有δ13C1<-38‰、δ13C2<-28‰的特征。下古生界地层包裹体中气体与气藏中气体地球化学性质对比表明,下古生界气田天然气乙烷碳同位素的变化范围也比甲烷碳同位素的变化范围大很多,乙烷碳同位素不适合作为判断靖边气田天然气来源的标准。在此基础上,以上古生界天然气甲烷碳同位素的平均值(-32.90‰)与下古生界δ13C1<-38‰天然气甲烷碳同位素的平均值(-39.04‰)分别作为上、下古生界来源天然气甲烷碳同位素的界限值,通过简单计算认为靖边气田大约85%的天然气来源于上古生界煤系。  相似文献   

9.
测定了新疆罗布泊地区湖相沉积物CK-2钻孔样品的总有机碳含量（TOC）及其同位素组成、碳酸盐含量和C/N比值等环境代用指标,以及石膏矿物的质谱-铀系年龄。测试结果表明,20～9kaB.P.期间沉积物δ13Corg.在-23.4‰～-16.1‰之间波动且阶段性明显,与TOC呈现良好的相关关系,整体变化趋势同南极Dome C冰芯中记录的全球大气CO2浓度一致;C/N比值表明有机碳来源主要是陆生高等植物。因此大气CO2浓度变化是影响20～9kaB.P.期间罗布泊湖相沉积物δ13Corg.值变化的主导因素,周围山体上C3/C4植物相对生物量的变化则是另一重要因素。依据δ13Corg.的变化序列将此时间段湖区古环境的演化分成6个阶段:20.0～14.1kaB.P.期间受到末次盛冰期的影响,气温偏低,湖水丰沛;14.1～13.3kaB.P.是一个气候不稳定期,冷暖波动较频繁,但以暖为趋势;13.3～12.8kaB.P.期间经历了一段冷期,于12.8kaB.P.结束了末次冰期,随后气候开始转暖至11.8kaB.P.;其后气温再次变冷并维持到10kaB.P.;最后从10kaB.P.进入全新世暖期。δ13Corg.序列明显向偏负方向变化,表明该地区变暖的趋势相当明显。罗布泊地区日益干旱化是全球气候变化的结果,尤其是受到全球CO2浓度的不断升高所制约。  相似文献   

10.
当前气候变暖是一个全球面临的重大问题,它对人类赖以生存的植被生态系统造成的影响已经在全球各地逐步显现出来。为了深入了解植物生态系统对环境和气候变化的响应机制,我们需要更好地借鉴地质历史时期气候环境和植物协同演化的重要事件。C4植物作为陆地生产力较强的植物,在植物生态演化中占举足轻重的地位。目前研究表明C4植物可能最晚起源于始新世-渐新世之交,但从它早期起源到随后在生态系统中的大规模扩张时间间隔长达20多个百万年。是什么因素导致了C4植物的起源和扩张是一个悬而未决的重要问题,需要开展大量的调查研究来评估和重建C4植物在过去生态系统中的相对生物量变化。重建C4植物的含量目前主要的方法是建立在C3/C4植物碳同位素和植物内部结构形态差异基础之上。最常运用的研究材料包括(古)土壤有机质、成壤碳酸盐、陆地食草动物体组织、沉积物生物标志物、孢粉、植硅体等。这些方法在重建现代以及地质历史时期C4植物相对生物量变化的研究中发挥了重要作用,但同时也存在很多无法避免的问题。本文介绍了C4植物起源和扩张机制的主流观点以及不同研究材料的碳同位素所推算C4植物生物量的基本原理,并以柴达木盆地大红沟剖面为例,针对新生代湖泊沉积物中陆生高等植物的长链正构烷烃特征和单体烃碳同位素的研究结果,详细讨论C4植物含量重建的方法与缺点,为探讨C4植物起源、演化及控制因素提供参考。我们通过分析前人研究的大红沟剖面长链正构烷烃及单体烃 δ13Calk 值特征,推测在30~24 Ma、20~17 Ma和13~7 Ma期间δ13Calk值显示相对正偏的原因,可能是干旱和C4植物在当地生态系统中出现的双重因素叠加造成的。但这一推断还需要借助于新的研究方法,即单颗粒孢粉碳同位素的方法来提供C4植物的确凿证据。  相似文献   

11.
To understand reaction pathways and isotope systematics during mineral-catalyzed abiotic synthesis of hydrocarbons under hydrothermal conditions, experiments involving magnetite and CO2 and H2-bearing aqueous fluids were conducted at 400 °C and 500 bars. A robust technique for sample storage and transfer from experimental apparatus to stable isotope mass spectrometer provides a methodology for integration of both carbon and hydrogen isotope characterization of reactants and products generated during abiogenic synthesis experiments. Experiments were performed with and without pretreatment of magnetite to remove background carbon associated with the mineral catalyst. Prior to experiments, the abundance and carbon isotope composition of all carbon-bearing components were determined. Time-series samples of the fluid from all experiments indicated significant concentrations of dissolved CO and C1-C3 hydrocarbons and relatively large changes in dissolved CO2 and H2 concentrations, consistent with formation of additional hydrocarbon components beyond C3. The existence of relatively high dissolved alkanes in the experiment involving non-pretreated magnetite in particular, suggests a complex catalytic process, likely involving reinforcing effects of mineral-derived carbon with newly synthesized hydrocarbons at the magnetite surface. Similar reactions may be important mechanisms for carbon reduction in chemically complex natural hydrothermal systems. In spite of evidence supporting abiotic hydrocarbon formation in all experiments, an “isotopic reversal” trend was not observed for 13C values of dissolved alkanes with increasing carbon number. This may relate to the specific mechanism of carbon reduction and hydrocarbon chain growth under hydrothermal conditions at elevated temperatures and pressures. Over time, significant 13C depletion in CH4 suggests either depolymerization reactions occurring in addition to synthesis, or reactions between the C1-C3 hydrocarbons and carbon species absorbed on mineral surfaces and in solution.  相似文献   

12.
New drill cores from the Lower Aptian historical stratotype at Roquefort-La Bédoule (SE France) provide continuous high-resolution geochemical and isotope records which closely track the onset of OAE 1a in a subtropical intra-shelf basin (South Provençal Basin). The drilling operation recovered a total of 180 m of undisturbed sediments in three holes. The lowermost 67 m correspond to the Bedoulian (core LB1) and are here analyzed in high-resolution using geochemical proxies (stable carbon isotopes, stable oxygen isotopes, and carbonate content) and foraminiferal biostratigraphy. Pervasive bioturbation through core LB1 suggests mostly oxygenated bottom water conditions with transient dysoxic episodes, as shown by higher pyrite and glauconite concentrations within the marlstones. Unprecedented resolution over the negative δ13C excursion preceding OAE 1a (segment C3) reveals a characteristic double trough extending over ∼5.5 m in core LB1. This long-lasting negative excursion was possibly linked to multiple pulses of enhanced CO2 release to the atmosphere. Estimated sedimentation rates of 1.6–2 cm/kyr indicate that the negative δ13C excursion lasted >200 kyr, while the main positive carbon isotope shift (segment C4) had a duration of >300 kyr. Fluctuations in δ18O suggest transient episodes of climate warming and cooling at the northern margin of the Tethys or even on a more global scale prior to the onset of OAE 1a.  相似文献   

13.
对北黄海盆地侏罗系两块含油砂岩的抽提物进行了常规的有机地球化学分析和碳同位素测试,结果表明它们具有不同的地球化学特征:埋藏较深的油砂抽提物属正常原油,饱和烃以正构烷烃为主,色谱图显示单峰型正态分布;而埋藏较浅的油砂抽提物,在饱和烃色谱图中有明显的UCM鼓包,同时含有完整的低碳数的正构烷烃、姥鲛烷和植烷,全油及族组成碳同位素分布范围广,为-24.7‰~-32.3‰,其中,全油及沥青质碳同位素偏重,饱和烃和芳烃碳同位素轻,反映出遭受了强烈的生物降解作用。与成熟度相关的生物标志物参数显示,原油已进入成熟—高成熟阶段。生物标志物和碳同位素组成表明,母质是在水体较浅的湖相环境下沉积的,受陆源高等植物和低等水生藻类的双源控制。综合判断,研究区存在两期油气充注。  相似文献   

14.
A study was carried out to test the usefulness of surface geochemical methods as regional evaluation tools in petroliferous region of the Mehsana block, North Cambay Basin. A suite of 135 soil samples collected from the depth of 2.5 m, were analyzed for adsorbed light gaseous hydrocarbons and carbon isotopes (δ13Cmethane and δ13Cethane). The light gaseous hydrocarbon analysis show that the concentration ranges 402 ppb, 135 ppb, 70 ppb, 9 ppb and 18 ppb of C1, C2, C3, iC4 and nC4, respectively. The value of carbon isotopic ranges of methane −29.5 to −43.0‰ (PDB) and ethane −19.1 to −20.9‰ (PDB). This data, when mapped, indicates patterns coinciding with major known oil and/or gas field of Sobhasan/Linch in this study area. The existence of un-altered petroliferous microseeps of catagenetic origin is observed in the study area. A regional study, such as the one described here, can provide important exploration facts concerning the regional hydrocarbon potential in a block. This method has been confirmed and can be applied successfully in frontier basins.  相似文献   

15.
To better understand chemical weathering and controlling processes in the Yalong River of the eastern Tibetan Plateau, this study presents major ion concentrations and stable isotopes of the dissolved loads. The isotopic compositions (δ13C-DIC, δ34S and δ18O-SO4) of the dissolved loads are very useful to quantify solute sources and define the carbon budget related with chemical weathering in riverine systems. The isotopic composition of sulphate demonstrates that most of the sulphate is derived from sulphide oxidation, particularly in the upper reach of the Yalong River. The correlations between δ13C-DIC, water chemistry and isotopes of sulphate, suggest that the carbon dynamics are mainly affected by carbonate weathering by sulphuric acid and equilibration processes. Approximately 13% of the dissolved inorganic carbon in the Yalong River originates from carbonate weathering by strong acid. The CO2 consumption rates are estimated to be 2.8 × 105 mol/km2/yr and 0.9 × 105 mol/km2/yr via carbonate and silicate weathering in the Yalong River, respectively. In this study, the influence of sulphide oxidation and metamorphic CO2 on the carbon budget is estimated for the Yalong River draining the eastern Tibetan Plateau.  相似文献   

16.
The isotopic composition of dissolved inorganic carbon （DIC） in estuarine environments has been studied for its significant role in determining the isotopic composition of inorganic/organic matter and its applications to the study of various natural processes. In this paper, based on the stable isotope geochemical characteristics of dis- solved inorganic carbon in the Jiulong River Estuary, the following conclusions are drawn： （1） δ13CDIC values are mainly controlled by the mixing ratio of fresh water and sea water; （2）δ13Cphytoplankton values are linearly related to the δ13CDIC values; （3） δ13CpoM values for the Jiulong River Estuary are affected by anthropogenic pollution signifi- cantly; and （4） the comprehensive analysis of δ13Cphytoplankton, δ13CpoM and δ13CDIc shows that along with increasing salinity, the proportion of POM derived from the degradation of phytoplanktons gradually increases.  相似文献   

17.
东明凹陷土壤吸附烃的石油化探效果   总被引：3，自引：1，他引：3  
李鹤庆  王福 《物探与化探》1991,15(6):459-464
经过对吸附烃各指标的对比研究,发现C3+①指标不受地表干扰因素的影响,它的异常反映的可能是地下油气的信息。用C3+指标圈定了五个异常,其中Ⅰ号异常已经钻出了工业油流;Ⅱ、Ⅲ号异常有很大的油气勘探价值;Ⅳ号异常也有一定的勘探意义;Ⅴ号异常没有勘探价值。同时,地温的Ⅴ号异常已经发展成油田,称三春集油田。水化学的二级异常(Ⅱ2)也钻出了工业油流。这是对地球化学法勘探油气田有效性的有力验证。  相似文献   

18.
Groundwater and surface water samples were collected to improve understanding of the Senegal River Lower Valley and Delta system, which is prone to salinization. Inorganic ion concentrations and environmental isotopes (18O, 2H and 3H) in groundwater, river, lake and precipitation were investigated to gain insight into the functioning of the system with regard to recharge sources and process, groundwater renewability, hydraulic interconnection and geochemical evolution. The geochemical characteristics of the system display mainly cation (Ca2+ and/or Na+) bicarbonated waters, which evolve to chloride water type; this occurs during groundwater flow in the less mineralized part of the aquifer. In contrast, saline intrusion and secondary brines together with halite dissolution are likely to contaminate the groundwater to Na–Cl type. Halite, gypsum and calcite dissolution determine the major ion (Na+, Cl−, Ca2+, Mg2+, SO4 2− and HCO3 −) chemistry, but other processes such as evaporation, salt deposition, ion exchange and reverse exchange reactions also control the groundwater chemistry. Both surface water and groundwater in the system show an evaporation effect, but high evaporated signatures in the groundwater may be due to direct evaporation from the ground, infiltration of evaporated water or enriched rainwater in this region. The stable isotopes also reveal two types of groundwater in this system, which geomorphologically are distributed in the sand dunes (depleted isotopes) and in the flood plain (enriched isotopes). Consideration of the 3H content reinforces this grouping and suggests two mechanisms of recharge: contribution of enriched surface water in recharging the flood plain groundwater and, in the sand dunes area where water table is at depth between 8 and 13 m, slow recharge process characterized the submodern to mixed water.  相似文献   

19.
《Applied Geochemistry》2005,20(11):2116-2137
Samples of mine water from Butte, Montana were collected for paired geochemical and stable isotopic analysis. The samples included two sets of depth profiles from the acidic Berkeley pit lake, deep groundwater from several mine shafts in the adjacent flooded underground mine workings, and the acidic Horseshoe Bend Spring. Beginning in July-2000, the spring was a major surface water input into the Berkeley pit lake. Vertical trends in major ions and heavy metals in the pit lake show major changes across a chemocline at 10–20 m depth. The chemocline most likely represents the boundary between pre-2000 and post-2000 lake water, with lower salinity, modified Horseshoe Bend Spring water on top of higher salinity lake water below. Based on stable isotope results, the deep pit lake has lost approximately 12% of its initial water to evaporation, while the shallow lake is up to 25% evaporated. The stable isotopic composition of SO4 in the pit lake is similar to that of Horseshoe Bend Spring, but differs markedly from SO4 in the surrounding flooded mine shafts. The latter is heavier in both δ34S and δ18O, which may be due to dissolution of hypogene SO4 minerals (anhydrite, gypsum, barite) in the ore deposit. The isotopic and geochemical evidence suggests that much of the SO4 and dissolved heavy metals in the deep Berkeley pit lake were generated in situ, either by leaching of soluble salts from the weathered pit walls as the lake waters rose, or by subaqueous oxidation of pyrite on the submerged mine walls by dissolved Fe(III). Laboratory experiments were performed to contrast the isotopic composition of SO4 formed by aerobic leaching of weathered wallrock vs. SO4 from anaerobic pyrite oxidation. The results suggest that both processes were likely important in the evolution of the Berkeley pit lake.  相似文献   

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