大洋玄武质岩石元素间的线性关系及其应用

批式熔融是大洋玄武质岩石形成的主要机制之一。本文建立了批式熔融作用中元素间的线性关系模型,并应用于北秦岭宽坪群变玄武质岩石化学分析资料的研究,对变异图解、相关矩阵、源区成分计算和估计等问题作了讨论。给出了一些具体应用的方法。     

Investigations on the petroleum generation potential of bituminous coals from the Saar region

The Saar basin contains bituminous coals (high volatile A and B). Five coals of Westphalian and Stephanian age with distinctly varying maceral compositions were analysed by Soxhlet extraction and supercritical extraction with different solvents and microscopically. From the data obtained it is concluded that the oldest coals have a potential for oil generation, whereas the younger coals do not. This conclusion is explained by varying liptinite contents and varying adsorption capacities of different vitrinite macerals for bitumen.     

Tertiary deltaic and lacustrine organic facies: comparison of biomarker and kerogen distributions

Biological marker and kerogen compositional data in Tertiary deltaic and lacustrine settings were compared and contrasted. The two settings are represented by (a) coals and organic-carbon-rich shales in a ick deltaic sequence from the Far East, constituting three distinct organic facies, and (b) humic coals and spropelic oil shales in a restricted intermontane (freshwater) lacustrine sequence from western Montana (U.S.A.), constituting two distinct organic facies. Wedistinguish the organic facies in each depositional setting by systematic differences in gross compound class distributions, kerogen and infrared spectral characteristics, molecular character of pyrolyzates, sterane carbon number distribution and sterane/hopane ratios. The kerogens of the three deltaic organic facies are characterized by varying quantities of vitrinite, resinite, sporinite, cutinite and fluorescent amorphinite. Triterpane distributions reveal numerous terrigenous compounds, including oleanane, oleanenes and unidentified C₃₀ (presumably) resin-derived components. The two organic facies of the freshwater lacustrine setting are distinguishedased upon either a vitrinite or an alganite/fluorescent amorphinite predominance in the kerogen. Numerous characteristics facies-related markers are also present, including dehydroabietane (land plant resins) and 4-methylsteranes (perhaps from freshwater dinoflagellate input). The available molecular and petrographic data are evaluated, and characteristics are proposed for distinguishing five organic facies of these two depositional settings. The successful simultaneous use of molecular geochemistry and organic petrography in this study provides a format for refining the organic facies concept.     

泰山玉的致色因素分析

颜色是珠宝玉石宝石学特征研究的重要一项,是影响宝玉石价值的重要因素。泰山玉有4个颜色系列,对各系列泰山玉致色因素的分析研究具有重大意义。通过化学分析和电子探针测试,查明了泰山玉的主要化学成分,对比分析了化学成分与颜色的关系,最终确定了不同颜色系列泰山玉的致色因素。     

N2 fixation variability in the oligotrophic Sulu Sea, western equatorial Pacific region over the past 83 kyr

N₂ fixation is an important biological process that adds new nitrogen to oceans and plays a key role in modulating the oceanic nitrate inventory. However, it is not known how, when, and where N₂ fixation rates have varied in response to past climate changes. This study presents a new record of nitrogen isotopic composition (δ¹⁵N) over the last 83 kyr from a sediment core (KH02-4 SUP8) taken in the Sulu Sea in the western equatorial Pacific region; data allow the N₂ fixation variability in the sea to be reconstructed. Sediments, sinking, and suspended particulate organic matter (POM) all have lighter isotopic values compared to the δ¹⁵N values of substrate nitrate (av. 5.8‰) in North Pacific Intermediate Water. These lighter δ¹⁵N values are regarded as reflecting N₂ fixation in the Sulu Sea surface water. A δ¹⁵N mass balance model shows that N₂ fixation rates were significantly enhanced during 54–34 kyr in MIS-3 and MIS-2. It has been speculated that higher interglacial denitrification rates in the Arabian Sea and the eastern tropical Pacific would have markedly decreased the global oceanic N inventory and contributed to the increase in N₂ fixation in oligotrophic regions, but such a model was not revealed by our study. It is possible that changes in N₂ fixation rates in the Sulu Sea were regional response, and accumulation of phosphate in the surface waters due to enhanced monsoon-driven mixing is thought to have stimulated enhancements of N₂ fixation during MIS-3 and MIS-2.     

济阳坳陷前古近纪烃源岩生烃潜力分析

济阳坳陷前古近系发育多套低勘探程度层系,下古生界寒武系—奥陶系、上古生界石炭系—二叠系和中生界都具有一定的生烃能力并可以提供油气资源。不同地质时期构造和沉积背景的差异形成了具有不同地球化学特征的烃源岩。本文综合地质资料、烃源岩热解和TOC分析资料、镜质体反射率资料、全岩显微组分分析资料、饱和烃和芳香烃色质资料等,系统分析了济阳坳陷前古近系烃源岩分布特征、地化特征和资源潜力。下古生界海相碳酸盐岩系烃源岩分布局限,有机质丰度较低,但类型较好,具有一定的供烃能力。上古生界煤系烃源岩分布范围广,有机质丰度较高,有机质类型相对较差,以生气为主,复杂的构造演化特征导致了这套源岩以二次生气为主。中生界发育了煤系源岩和湖相泥岩两套烃源岩,有机质类型中等,局部发育中等—好烃源岩,成熟度空间差异较大。总体来看,济阳坳陷三套前古近系烃源岩中,上古生界煤系源岩品质最佳,中生界次之,下古生界相对较差。     

煤炭显微煤岩组分与工业分析关系研究

通过分析宁夏各煤田中部分具有代表性煤矿勘查阶段钻孔煤岩煤样测试数据,研究了煤的显微煤岩组分与工业分析之间的关系。随着煤中有机组分、无机组分含量的变化,煤的灰分、挥发分、固定碳发生变化。煤中有机组分含量大于90%时,煤中灰分与黏土类含量存在正相关,挥发分与惰质组和壳质组含量均存在正相关,且惰质组含量影响更大;有机组分含量小于90%时,煤中灰分与惰质组和黏土类含量均存在正相关,且惰质组含量影响更大,挥发分与壳质组含量存在正相关。煤中固定碳含量受镜质组含量影响最大,二者存在正相关。     

机器学习在岩矿地球化学研究中的应用——综述与思考

岩石与矿物的地球化学成分数据具有高维度特征。传统的岩矿地球化学成分研究主要采用二元/三元图解判别法,准确率不高,在数理统计方法上有欠缺。机器学习方法非常适用于对大样本高维度的岩矿成分数据进行数理统计处理。本文在介绍机器学习常见算法基本原理的基础上,总结近5年来国内外学者将机器学习方法应用于岩石矿物成分数据研究的实例,包括：① 根据矿物成分溯源其母岩（源岩）、判别矿床类型,② 新生代火山岩溯源,③ 判别变质岩原岩,④ 依据岩浆岩成分判别大地构造环境等。已有的研究实例显示,机器学习方法的准确度明显优于传统的低维度判别法。机器学习本质是分析大样本数据的高维度变量之间的相关、归类等多元统计问题。推广机器学习的应用需要建设开放获取（Open Access）的矿物、岩石成分数据库,同时全面实施开放研究（Open Research）的发表策略。     

内蒙古东胜地区砂岩型铀矿赋矿地层方解石胶结物C、O同位素特征和成因模型

砂岩型铀矿赋矿地层方解石胶结物C、O同位素组成对研究成矿机制具有重要的理论和实践意义。前人在成矿流体来源定性判断方面做了大量的研究工作,但缺乏对成矿混合流体的组分特征及相关参数的定量认识。根据内蒙古东胜地区东南部皂火壕和西北部纳岭沟铀矿床赋矿地层直罗组方解石胶结物C、O同位素组成特征,建立了渗出热卤水和渗入地层水两种不同流体混合生成方解石胶结物C、O同位素组成定量成因模型,并研究了两种流体来源、溶解碳的浓度比、流体比例以及热液温度等综合因素。除少数样品方解石胶结物为地层沉积时形成外,大部分方解石胶结物是热卤水与地层水两种流体混合作用的结果,古生界有机酸脱羧作用导致热卤水中富含CO_2。东胜地区砂岩型铀矿成矿流体地层水与热卤水比例为0.5～0.9,地层水所占的比例较大;热卤水与地层水溶解碳浓度比主要范围为1.5～5.0,部分大于10.0,热卤水中溶解碳浓度较高,是富含CO_2的流体。混合流体温度分为两个主要范围55～80℃、90～140℃,结合古盐度和盐度指数反演,表明成矿流体为有机与无机混合成因的低温热液流体。用砂岩型铀矿赋矿地层方解石胶结物C、O同位素组成,可定量模拟两种流体溶解碳浓度比、流体比例和方解石形成时温度等流体成矿条件,解释碳酸盐胶结物成因,以便从成矿流体角度更好地理解成矿作用过程。     

内蒙古东胜地区砂岩型铀矿赋矿地层方解石胶结物C、O同位素特征和成因模型

砂岩型铀矿赋矿地层方解石胶结物C、O同位素组成对研究成矿机制具有重要的理论和实践意义。前人在成矿流体来源定性判断方面做了大量的研究工作,但缺乏对成矿混合流体的组分特征及相关参数的定量认识。根据内蒙古东胜地区东南部皂火壕和西北部纳岭沟铀矿床赋矿地层直罗组方解石胶结物C、O同位素组成特征,建立了渗出热卤水和渗入地层水两种不同流体混合生成方解石胶结物C、O同位素组成定量成因模型,并研究了两种流体来源、溶解碳的浓度比、流体比例以及热液温度等综合因素。除少数样品方解石胶结物为地层沉积时形成外,大部分方解石胶结物是热卤水与地层水两种流体混合作用的结果,古生界有机酸脱羧作用导致热卤水中富含CO2。东胜地区砂岩型铀矿成矿流体地层水与热卤水比例为0.5~0.9,地层水所占的比例较大;热卤水与地层水溶解碳浓度比主要范围为1.5~5.0,部分大于10.0,热卤水中溶解碳浓度较高,是富含CO2的流体。混合流体温度分为两个主要范围55~80℃、90~140℃,结合古盐度和盐度指数反演,表明成矿流体为有机与无机混合成因的低温热液流体。用砂岩型铀矿赋矿地层方解石胶结物C、O同位素组成,可定量模拟两种流体溶解碳浓度比、流体比例和方解石形成时温度等流体成矿条件,解释碳酸盐胶结物成因,以便从成矿流体角度更好地理解成矿作用过程。