Multiple isotopes (C-S-N-H) and bound biomarkers in asphaltenes: New constraints on the classification and genesis of reservoir bitumens from the northwestern Sichuan Basin, South China

IF 2.6 3区 地球科学 Q2 GEOCHEMISTRY & GEOPHYSICS
Susu Wang , Jian Chen , Wanglu Jia , Ping’an Peng
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Abstract

Reservoir bitumens in the northwestern Sichuan basin are significant for elucidating the sources and charging history of oil and gas, given their widespread occurrence in multiple strata in the area and abundant biomarkers. The debate regarding the origin and genesis of these bitumens has persisted for a long time, due to severe biodegradation and the development of multiple sets of high maturity source rocks with few biomarkers for oil-source correlation. To resolve these questions, asphaltenes, which are more resistant to biodegradation than free hydrocarbons, were systematically analyzed with the bulk multi-isotopes (C-S-N-H), bound molecules and the carbon isotopic compositions of bound individual n-alkanes. These characteristics were then compared to those of bulk bitumen and free hydrocarbons, leading to three main conclusions. In most samples, relatively abundant 25-norhopanes and 17-nortricylic terpanes were identified along with n-alkanes in free hydrocarbons, suggesting at least two oil charging events. In the samples having free n-alkanes, the carbon isotopic compositions of asphaltene-bound n-alkanes closely resemble those of corresponding free n-alkanes. Moreover, the bulk C-S-N isotopic compositions of asphaltene also approach those of corresponding bulk bitumen. These results suggest that the source of the oil charges occuring at different times are mostly the same for an individual sample, though different bitumen samples may have distinct sources. Free hydrocarbons, including n-alkanes and biomarkers, may have been produced by the secondary cracking of asphaltenes. Second, the integration of bulk C-S-N isotopic compositions of the asphaltenes and bitumens has enabled the studied samples to be classified into four groups. Source facies is the primary control of the distinct isotopic compositions with other factors like biodegradation, thermal maturity and migration having only minor influence. In combination with biomarkers, the organic matter and sedimentary environment of source rocks could be characterized for each group. A careful comparison of the bulk C-S-N isotopic compositions of asphaltenes and bitumens with those previously reported for source rocks (organic C and S and bulk N isotopes) suggests the main source rocks in the Upper Ediacarian-Lower Cambrian Formations, supporting the conclusions of previous studies. Furthermore, those source rocks in much younger formations, such as the Middle Permian as well as the Middle Devonian Formations, may also have contributed significantly to the widespread reservoir bitumens in the region. These findings highlight the usefulness of bulk C-S-N isotopic composition of asphaltenes for distinguishing oils with complex genesis and large gas exploration potential of the Upper Paleozoic source rocks in the region.

沥青质中的多同位素(C-S-N-H)和结合生物标记:华南四川盆地西北部储层沥青质分类与成因的新约束
四川盆地西北部的储层沥青质广泛存在于该地区的多个地层中,并具有丰富的生物标志物,因此对于阐明油气的来源和充注历史具有重要意义。由于严重的生物降解和多套高成熟度源岩的发育,以及用于油源关联的生物标志物很少,有关这些沥青质的来源和成因的争论一直持续了很长时间。沥青质比游离碳氢化合物更耐生物降解,为了解决这些问题,我们系统地分析了沥青质的多同位素(C-S-N-H)、结合分子以及结合的单个正构烷烃的碳同位素组成。然后将这些特征与块状沥青和游离碳氢化合物的特征进行了比较,得出了三个主要结论。在大多数样本中,除了游离碳氢化合物中的正构烷烃外,还发现了相对丰富的 25-正构烷烃和 17-正构萜烯,这表明至少发生过两次石油充填事件。在具有游离正构烷烃的样本中,与沥青结合的正构烷烃的碳同位素组成与相应的游离正构烷烃非常相似。此外,块状沥青质的 C-S-N 同位素组成也接近于相应块状沥青的 C-S-N 同位素组成。这些结果表明,尽管不同的沥青样品可能有不同的来源,但不同时间出现的油荷来源对于单个样品来说大多是相同的。游离碳氢化合物(包括正构烷烃和生物标记物)可能是由沥青质二次裂解产生的。其次,通过整合沥青质和沥青的大体积 C-S-N 同位素组成,可以将所研究的样本分为四组。源面是控制不同同位素组成的主要因素,生物降解、热成熟度和迁移等其他因素的影响较小。结合生物标志物,可以确定每组源岩的有机物质和沉积环境特征。将沥青质和沥青气的大体积 C-S-N 同位素组成与之前报告的源岩(有机 C 和 S 以及大体积 N 同位素)进行仔细比较后发现,主要的源岩位于上埃迪卡拉-下寒武纪地层,这支持了之前研究的结论。此外,二叠纪中期和泥盆纪中期地层等更年轻地层中的源岩也可能对该地区广泛存在的储层沥青做出了重要贡献。这些发现突出表明,沥青质的大体积 C-S-N 同位素组成有助于区分该地区上古生界源岩中成因复杂的油类和具有巨大天然气勘探潜力的油类。
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来源期刊
Organic Geochemistry
Organic Geochemistry 地学-地球化学与地球物理
CiteScore
5.50
自引率
6.70%
发文量
100
审稿时长
61 days
期刊介绍: Organic Geochemistry serves as the only dedicated medium for the publication of peer-reviewed research on all phases of geochemistry in which organic compounds play a major role. The Editors welcome contributions covering a wide spectrum of subjects in the geosciences broadly based on organic chemistry (including molecular and isotopic geochemistry), and involving geology, biogeochemistry, environmental geochemistry, chemical oceanography and hydrology. The scope of the journal includes research involving petroleum (including natural gas), coal, organic matter in the aqueous environment and recent sediments, organic-rich rocks and soils and the role of organics in the geochemical cycling of the elements. Sedimentological, paleontological and organic petrographic studies will also be considered for publication, provided that they are geochemically oriented. Papers cover the full range of research activities in organic geochemistry, and include comprehensive review articles, technical communications, discussion/reply correspondence and short technical notes. Peer-reviews organised through three Chief Editors and a staff of Associate Editors, are conducted by well known, respected scientists from academia, government and industry. The journal also publishes reviews of books, announcements of important conferences and meetings and other matters of direct interest to the organic geochemical community.
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