Organic facies and geochemical aspects in Neogene neritic sediments of the Takafu syncline area of central Japan: Paleoenvironmental and sedimentological reconstructions

Abstract Organic petrological observations of kerogen macerals and organic geochemical analyses of carbon isotopes of kerogen macerals and biomarkers were conducted on Neogene neritic sediments of the Takafu syncline area of central Japan. The Senmi, Sakainomiya and Lower Shigarami Formations in that area were deposited at the neritic provinces on the southern edge of the paleo‐Japan Sea during the Late Miocene to Early Pliocene. Sedimentary organic matter in these formations was almost terrigenous in origin. Changes in kerogen maceral compositions reflect sedimentological and tectonic histories evaluated in previous studies from sedimentary facies and paleontology. It was found that carbon isotope ratios (δ¹³C) of kerogen macerals increased from ?28‰ to ?25‰ from the Sakainomiya to the lower part of the Lower Shigarami Formations. The cause of that increase was presumably the expansion of C₄ plants into southwest Japan. The timing was concordant with that of the expansion of C₄ plant grasslands in East Asia. The oxicity (oxic to anoxic) conditions of sea bottoms evaluated from pristane/phytane ratios varied. Particularly, in the lower part of the Senmi Formation, layers in which no steroid biomarkers could be detected were found, and had presumably formed under oxic conditions when strong biodegradation had occurred. Concentrations of regular (C₂₇–C₂₉) steranes and dinosteranes were higher in the Sakainomiya and Lower Shigarami Formations. This indicates that dinoflagellates‐dominant primary productions were higher at those stages. In addition, concentrations of diatomaceous biomarkers such as C₂₆ norsterane increased from the Lower Shigarami Formation, thus adding diatoms to the major producers. Furthermore, similar associations between the increases of δ¹³C values of kerogen macerals and concentrations of diatomaceous biomarkers were observed in the Takafu syncline area. Thus, the expansion of C₄ plants was possibly associated with the high production of diatom in the shallow‐marine areas of the paleo‐Japan Sea during the Neogene Period.     

鄂尔多斯北部直罗组中烃类包裹体地球化学特征及来源分析

对鄂尔多斯盆地东胜地区中侏罗统直罗组砂岩中烃类包裹体进行镜下观察、描述，利用压碎抽提法对烃类包裹体进行色谱—质谱分析，并与白垩系油苗、三叠系油砂及源岩抽提物进行对比，目的是探讨其来源。包裹体油生物标志物成熟度参数，C29ααα甾烷20S/(S+R)、C32αβ藿烷22S/(S+R)比值基本达到平衡值，利用甲基菲指数计算的镜质体反射率参数介于0.64%～0.82％之间，显示包裹体中石油烃已接近成熟—成熟热演化阶段；物质来源及沉积环境参数，ααα20R甾烷百分含量C27>C28相似文献   

The Atmospheric Oxidation of the HS Radical: Reaction with NO2

The atmospheric reaction between HS and NO₂ was theoretically investigated at 298 K and 1 atm of pressure. Our results show that the first reaction step will lead to the formation of HSNO₂ or HSONO, spontaneously and exothermically. HSONO easily decomposes into HSO + NO. On the other hand, HSNO₂ can hardly dissociate in the reactants, and its isomerization to other adducts is much hindered. Production of HNO + SO and SNO + OH was found to be unfavorable. Thus, the main products would be HSO + NO and HSNO₂, and new investigations focusing on the atmospheric fate of HSNO₂ are suggested. A general discussion of the fate of HS under atmospheric conditions is presented. Recent investigations indicate that NO₂, O₂ and N₂O should be the most important oxidants of HS, while the O₃ influence will not be significant.     

百色盆地低熟油的地球化学特征及成因机制

对百色盆地几个典型低熟油进行了常规的有机地球化学分析,并重点以百－５井低熟油为对象,详细总结了饱和烃,芳烃生物标志物地球化学特征及其组合,结果表明陆生高等植物和微生物大量繁衍及其对高等植物的改造的贡献可能是形成百色盆地第三系低熟油的主要原因。     

傅立叶变换红外光谱联用技术在化石燃料分析中的应用

对傅立叶变换红外光谱联用技术在化石燃料分析中的应用进行了较全面的总结评述,重点介绍了气相色谱／红外光谱联机、高压液相色谱／红外光谱联机、薄层色谱／红外光谱联机、超临界流体色谱／红外光谱联机、裂解色谱／红外光谱联机、热重分析／红外光谱联机、气相色谱／红外光谱／质谱三机联用技术等在化石燃料的结构组分分析、成因机理研究及其勘探等诸方面的重要应用,尤其是在芳香族化合物和几何异构体的分离鉴定方面发挥出的突出功效。引用文献５９篇。     

对流层平流层气溶胶粒子的形态和化学组成

分析研究了１９９３年和１９９４年的８月、９月在香河地区上空采集的单个气溶胶粒子的形态及化学元素和化合物的组成。结果表明：１９９３年,在对流层大气中的气溶胶颗粒经常出现不规则形的粒子,可能是土壤粒子;而在平流层大气中的颗粒以具有“卫星”结构的硫酸粒子为主;硫酸铵粒子则经常出现在对流层的中、下部。香河地区上空颗粒物的化学元素组成比较复杂,单一化学元素组成的粒子较少,粒子主要含有Ｓｉ,Ｆｅ,Ａｌ和Ｓ等元素。气溶胶的化合物有硫酸盐、硅酸盐、硝酸盐和磷酸盐等     

南极半岛东北海域表层沉积有机质来源及其沉积环境

采用气相色谱-质谱技术对南极半岛东北海域海底表层沉积物的总有机碳、有机质碳同位素(δ13 Corg)和生物标志化合物等进行了测试分析。研究区表层沉积物总有机碳TOC平均值高于现代深海沉积物中的平均含量。δ13 Corg的变化说明该海域有机碳来源呈海洋水生生物来源和陆源混合的特征。正构烷烃的峰型分布、主峰碳、饱和烃轻重比C-21/C+22和(C21+C22)/(C28+C29)、甾烷组合和藿烷组合证实研究区西部表层沉积物有机质来源以陆源高等植物为主,其陆源可能来自于附近的南极半岛和南舍得兰群岛;研究区东部表层沉积物有机质来源偏以海源为主,且以低等浮游生物、藻类及细菌生物等海源输入为主。碳优势指数(Carbon preference index,CPI)、奇偶优势指数(Odd-even Predominance,OEP)和甾烷C29ααα20S/(20S+20R)比值显示研究区D1-7站位和D5-9沉积物有机质演化程度较高,D5-2和D2-4站位的有机质演化程度低,其他站位介于中间状态。饱和烃中姥鲛烷、植烷及其比值(Pr/Ph)等组合显示研究区西部以氧化-弱还原的沉积环境为主,其可能是受高温低盐别林斯高晋海水流和附近火山喷发的影响所致;研究区东部以还原—强还原沉积环境为主,可能是受低温高盐的威德尔底层水(WSBW)和威德尔海深层水(WSDW)影响所致。     

鄂尔多斯盆地西峰地区延长组烃源岩两环烷烃分布特征及其生源

鄂尔多斯盆地西南部西峰地区三叠系延长组烃源岩检出丰富的两环烷烃,主要为C12~C14和C15、C16两组两环烷烃。其相对丰度表现出3种源岩模式:1以低碳数两环烷烃为主,出现于长71和长81段非烃源岩;2两组两环烷烃都很丰富,出现于长73段富有机质烃源岩;3以高碳数两环烷烃为主,主要发现于长73段烃源岩,也见于长72和长81段。尽管长7段热演化程度基本一致,但补身烷异构化指数变化明显,表明补身烷重排不仅受热演化的影响,而且受有机质来源和沉积环境的控制。延长组烃源岩具有明显的高补身烷优势,反映了烃源岩的还原性沉积环境。烃源岩高丰度C15、C16两环烷烃的检出则指示该地区晚三叠世发育淡水湖泊。葡萄藻不仅是该地区中生界石油的重要母质来源,而且可能是这些两环类标志物的直接生源。     

准噶尔盆地西北缘车排子凸起原油类型与油源

准噶尔盆地西北缘南部红车断裂带- 车排子凸起油气藏众多,原油物理化学性质和地球化学特征十分复杂,原油类型及其来源长期存在很大争议。本文在准噶尔盆地不同时代烃源岩生成原油典型地球化学特征与主要油源判识指标归纳总结的基础上,对红车断裂带- 车排子凸起原油地球化学特征和来源进行系统分析研究,将该区域原油分为五类,其中三类原油分别来源于二叠系湖相烃源岩、中—下侏罗统煤系烃源岩、古近系安集海河组湖相烃源岩,另外两类为混合原油,分别为来源于二叠系湖相烃源岩的生物降解稠油与中—下侏罗统煤系烃源岩生成的正常原油和古近系湖相烃源岩生成的正常原油的混合原油。红车断裂带石炭系—白垩系油藏原油主要来源于沙湾凹陷二叠系湖相烃源岩,车排子凸起东北部春风油田稠油来源于沙湾凹陷二叠系湖相烃源岩;车排子凸起东侧- 红车断裂带西侧新近系沙湾组油藏轻质原油来源于四棵树凹陷古近系湖相烃源岩;车排子凸起中部春光油田白垩系—古近系油藏稠油为二叠系来源稠油和侏罗系正常原油的混合原油,新近系沙湾组油藏稠油为二叠系来源稠油与新近系正常原油的混合原油;车排子凸起西部石炭系—古近系油藏轻质原油来源于四棵树凹陷中—下侏罗统煤系烃源岩,而新近系沙湾组油藏轻质原油来源于四棵树凹陷古近系湖相烃源岩。本文对准噶尔盆地西北缘南部地区油气藏成藏研究及区域油气勘探决策具有重要参考作用。     

基于傅里叶变换质谱的烃源岩成熟度评价方法及地质意义

<正>伴随非常规油气资源的勘探开发,油气资源开采的广度和深度进一步扩大,一定程度上缓解了我国油气供需矛盾、保障了我国能源安全,同时有力推动了能源结构战略转型。但同时也对能源地质研究工作提出了新的挑战。有机质成熟度是油气评价的重要参数之一,不同成熟阶段的有机质会对应产出不同成因、不同性质、不同质量的油气,如何准确评价沉积有机质成熟度是当前油气资源勘探开发工作的关键问题之一。前人在科研实践工作中从光学、化学、谱学等角度提出了适用条件各异的成熟度评价方法,在部分地质环境中获得了良好的应用效果,但已有的成熟度指标多受测定方法原理的制约导致其适用性不同程度受限(肖贤明等,2020),制约了油气资源的高质量勘探开发。