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Impact of volcanism on the formation and hydrocarbon generation of organic-rich shale in the Jiyang Depression, Bohai Bay Basin, China
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作者 Jia-Hong Gao xin-ping liang +5 位作者 Zhi-Jun Jin Quan-You Liu Chang-Rong Li Xiao-Wei Huang Ju-Ye Shi Peng Li 《Petroleum Science》 SCIE EI CAS CSCD 2024年第3期1539-1551,共13页
Globally,most organic-rich shales are deposited with volcanic ash layers.Volcanic ash,a source for many sedimentary basins,can affect the sedimentary water environment,alter the primary productivity,and preserve the o... Globally,most organic-rich shales are deposited with volcanic ash layers.Volcanic ash,a source for many sedimentary basins,can affect the sedimentary water environment,alter the primary productivity,and preserve the organic matter(OM)through physical,chemical,and biological reactions.With an increasing number of breakthroughs in shale oil exploration in the Bohai Bay Basin in recent years,less attention has been paid to the crucial role of volcanic impact especially its influence on the OM enrichment and hydrocarbon formation.Here,we studied the petrology,mineralogy,and geochemical characteristics of the organic-rich shale in the upper submember of the fourth member(Es_(4)^(1))and the lower submember of the third member(Es_(3)^(3))of the Shahejie Formation,aiming to better understand the volcanic impact on organic-rich shale formation.Our results show that total organic carbon is higher in the upper shale intervals rich in volcanic ash with enriched light rare earth elements and moderate Eu anomalies.This indicates that volcanism promoted OM formation before or after the eruption.The positive correlation between Eu/Eu*and Post-Archean Australian Shale indicates hydrothermal activity before the volcanic eruption.The plane graph of the hydrocarbon-generating intensity(S1+S2)suggests that the heat released by volcanism promoted hydrocarbon generation.Meanwhile,the nutrients carried by volcanic ash promoted biological blooms during Es_(4)^(1 )and Es_(3)^(3) deposition,yielding a high primary productivity.Biological blooms consume large amounts of oxygen and form anoxic environments conducive to the burial and preservation of OM.Therefore,this study helps to further understand the organic-inorganic interactions caused by typical geological events and provides a guide for the next step of shale oil exploration and development in other lacustrine basins in China. 展开更多
关键词 Volcanic ash Hydrocarbon generation Organic-rich shale Shahejie Formation Jiyang Depression
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Effects of alfalfa saponin extract on mRNA expression of Ldlr, LXRα, and FXR in BRL cells
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作者 xin-ping liang Dong-qiang ZHANG +4 位作者 Yan-yan CHEN Rui GUO Jie WANG Cheng-zhang WANG Ying-hua SHI 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE CAS CSCD 2015年第6期479-486,共8页
We studied the effects of alfalfa saponin extract(ASE) on low density lipoprotein receptor(Ldlr), liver X receptor α(LXRα), and farnesoid X receptor(FXR) in normal and hyperlipidemic Buffalo rat liver(BRL)... We studied the effects of alfalfa saponin extract(ASE) on low density lipoprotein receptor(Ldlr), liver X receptor α(LXRα), and farnesoid X receptor(FXR) in normal and hyperlipidemic Buffalo rat liver(BRL) cells. Normal and hyperlipidemic BRL cells were divided into eight groups: normal, or normal cells treated with 50, 100, and 150 mg/L ASE, hyperlipidemic, or hyperlipidemic cells treated with 50, 100, and 150 mg/L ASE. After treatment for 24 h, Ldlr, LXRα, and FXR m RNA expression levels were measured by quantitative real-time polymerase chain reaction(q RT-PCR). Data showed that m RNA expression of Ldlr in normal BRL cells was significantly up-regulated by ASE treatment and m RNA expressions of LXRα and FXR were significantly down-regulated both in normal and hyperlipidemic BRL cells after ASE treatment. Thus, ASE might ameliorate hepatic steatosis by regulating genes involved in cholesterol metabolism, including up-regulation of Ldlr as well as down-regulation of LXRα and FXR. 展开更多
关键词 Alfalfa saponin extract Hyperlipidemic BRL cells Cholesterol metabolism m RNA expression
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