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柴达木盆地新生代湖相叠层石沉积序列及古环境意义 被引量:6
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作者 曾令旗 伊海生 +1 位作者 夏国清 袁桃 《现代地质》 CAS CSCD 北大核心 2017年第6期1251-1260,共10页
气候、沉积环境和湖平面的演变直接或间接地影响湖相叠层石的生长,因而叠层石的出现可以作为此三者变化的判别标志。通过对比研究柴达木盆地西部地区西岔沟、长尾台两条新生代陆相地层剖面中近10个湖相叠层石的发育层位、垂向沉积序列,... 气候、沉积环境和湖平面的演变直接或间接地影响湖相叠层石的生长,因而叠层石的出现可以作为此三者变化的判别标志。通过对比研究柴达木盆地西部地区西岔沟、长尾台两条新生代陆相地层剖面中近10个湖相叠层石的发育层位、垂向沉积序列,表明叠层石主要发育于新生代两个气候温暖湿润的高湖面时期,而且叠层石沉积亦同时出现在青藏高原其他邻近陆相新生代盆地,显示区域性的大规模异常湿润性气候,以强蒸发和强降水的交替为特征;划分出的4种含叠层石基本沉积序列中,叠层石可在泥岩或砂砾岩硬底上生长,含叠层石灰岩层之上通常是细粒碎屑沉积或间断面,这暗示了叠层石的生长出现在滨湖、浅湖相次级湖泛面附近,或指示湖水的突然加深。 展开更多
关键词 湖相叠层石 沉积序列 中新世 高原湖泛事件 柴达木盆地
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CGSG系列标准物质元素分馏效应及主量微量元素单元内均匀性探究 被引量:6
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作者 吴石头 王亚平 +4 位作者 詹秀春 Andreas Kronz Klaus Simon 许春雪 田欢 《岩矿测试》 CAS CSCD 北大核心 2016年第6期612-620,共9页
探究CGSG系列标准物质(CGSG-1、CGSG-2、CGSG-4、CGSG-5)的元素分馏效应及均匀性问题有助于开展其质量评估和应用推广。本文采用电子探针(EMPA)和激光剥蚀电感耦合等离子体质谱(LA-ICP-MS)研究了CGSG标准物质中的元素分馏效应、主量和... 探究CGSG系列标准物质(CGSG-1、CGSG-2、CGSG-4、CGSG-5)的元素分馏效应及均匀性问题有助于开展其质量评估和应用推广。本文采用电子探针(EMPA)和激光剥蚀电感耦合等离子体质谱(LA-ICP-MS)研究了CGSG标准物质中的元素分馏效应、主量和微量元素单元内均匀性,并报道了主量和微量元素分析数据。结果表明,在50μm激光束斑下,CGSG系列标准物质的元素分馏效应可忽略不计。EMPA均匀性指数结果显示,CGSG标准物质主量元素的单元内均匀性满足要求;以MPI-DING标准物质为参照,LA-ICP-MS测试CGSG标准物质中的大多数微量元素的单元内均匀性良好。与已报道的数据相比,本文报道的EMPA主量元素数据偏差在2%以内;LA-ICP-MS主量元素数据偏差在5%以内,微量元素数据基本匹配,少数元素由于分析不确定度较大等原因,如Cr、Ge、Cd、As、Tl等与已报道数据偏差较大。总体上,本文报道的分析数据可为CGSG定值数据库提供进一步的补充。 展开更多
关键词 CGSG标准物质 元素分馏 均匀性检验 电子探针 激光剥蚀电感耦合等离子体质谱
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193nm ArF准分子激光系统对LA-ICP-MS分析中不同基体的剥蚀行为和剥蚀速率探究 被引量:22
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作者 吴石头 许春雪 +2 位作者 Klaus Simon 肖益林 王亚平 《岩矿测试》 CSCD 北大核心 2017年第5期451-459,共9页
探究LA-ICP-MS分析中不同基体的剥蚀行为和剥蚀速率,可为激光参数设定、基体匹配选择、数据质量保证等方面提供重要参考。本文研究了193 nm ArF准分子激光系统对人工合成/地质样品玻璃、常见矿物和粉末压片的剥蚀行为,同时探究了激光参... 探究LA-ICP-MS分析中不同基体的剥蚀行为和剥蚀速率,可为激光参数设定、基体匹配选择、数据质量保证等方面提供重要参考。本文研究了193 nm ArF准分子激光系统对人工合成/地质样品玻璃、常见矿物和粉末压片的剥蚀行为,同时探究了激光参数(束斑直径、能量密度和剥蚀频率)对剥蚀速率的影响情况。从剥蚀坑形貌可知,193nm ArF激光对玻璃和绝大多数矿物的剥蚀行为良好,但对石英相对较差,这可能与石英内含有微观包裹体,剥蚀过程中局部受热不均有关。粉末压片的剥蚀行为呈现出不可控,可通过提高粉末压片的压制压力或降低粉末颗粒的粒径来改善剥蚀行为;当剥蚀深度大于1.5倍束斑直径时,剥蚀速率随剥蚀深度的增加而逐渐减小,剥蚀深度最多可达束斑直径的两倍左右(RESOlution M-50型号激光系统,3.0 J/cm2激光能量密度);剥蚀速率随激光能量密度的增加而增大,但基本不受剥蚀频率(2~20 Hz)影响。不同基体具有特征的剥蚀速率,本文报道了43种基体的剥蚀速率参数,总体而言,NIST系列玻璃的剥蚀速率大于地质样品玻璃,碳酸盐矿物和硫化物矿物大于硅酸岩矿物,粉末压片大于玻璃和常见矿物。 展开更多
关键词 193nm ArF激光 剥蚀行为 剥蚀速率 能量密度
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激光剥蚀-电感耦合等离子体质谱:双外标结合基体归一定量校准策略 被引量:7
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作者 吴石头 王亚平 许春雪 《分析化学》 SCIE EI CAS CSCD 北大核心 2017年第7期965-972,共8页
定量校准策略是激光剥蚀电感耦合等离子体质谱(AICP-MS)分析技术的重要组成部分,直接影响分析数据的质量。本研究评估了现有玻璃标准物质定值不确定度的相对大小,并探究了NIST、MPI-DING和USGS系列玻璃标准物质之间的基体效应。结果表明... 定量校准策略是激光剥蚀电感耦合等离子体质谱(AICP-MS)分析技术的重要组成部分,直接影响分析数据的质量。本研究评估了现有玻璃标准物质定值不确定度的相对大小,并探究了NIST、MPI-DING和USGS系列玻璃标准物质之间的基体效应。结果表明,NIST610的定值不确定度优于其它玻璃标准物质,在本实验条件下,NIST、MPI-DING和USGS系列玻璃标准物质之间的基体效应可忽略不计。在此基础上提出了双外标结合基体归一定量校准策略,外标分别为NIST610和St Hs6/80-G。此策略克服了由于NIST610主量成分与地质样品差别大而造成的主量元素准确度差以及St Hs6/80-G中某些微量元素含量低、定值不确定度较大等缺点。对比采用3种定量校准策略(单外标NSIT610基体归一法、单外标St Hs6/80G基体归一法和双外标基体归一法)校准的ML3B-G数据可知,双外标基体归一法有效避免了单外标基体归一法的不足,并提高了分析数据的准确度。采用双外标结合基体归一定量校准策略校准了BCR-2G、CGSG-2和KL-2G中的主量元素和微量元素。结果表明,绝大多数分析数据在定值不确定度范围内,验证了此校准策略的实用性。同时,本研究得到的主量微量元素数据进一步补充了BCR-2G、CGSG-2和KL-2G的定值数据库。 展开更多
关键词 激光剥蚀-电感耦合等离子体质谱 定量标准策略 定值不确定度 基体效应 微区分析
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Deciphering fluid inclusions in high-grade rocks 被引量:3
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作者 Alfons van den Kerkhof Andreas Kronz Klaus Simon 《Geoscience Frontiers》 SCIE CAS CSCD 2014年第5期683-695,共13页
The study of fluid inclusions in high-grade rocks is especially challenging as the host minerals have been normally subjected to deformation, recrystallization and fluid-rock interaction so that primary in- clusions, ... The study of fluid inclusions in high-grade rocks is especially challenging as the host minerals have been normally subjected to deformation, recrystallization and fluid-rock interaction so that primary in- clusions, formed at the peak of metamorphism are rare. The larger part of the fluid inclusions found in metamorphic minerals is typically modified during uplift. These late processes may strongly disguise the characteristics of the "original" peak metamorphic fluid. A detailed microstructural analysis of the host minerals, notably quartz, is therefore indispensable for a proper interpretation of fluid inclusions. Cathodoluminescence (CL) techniques combined with trace element analysis of quartz (EPMA, LA- [CPMS) have shown to be very helpful in deciphering the rock-fluid evolution. Whereas high-grade metamorphic quartz may have relatively high contents of trace elements like Ti and A1, low- temperature re-equilibrated quartz typically shows reduced trace element concentrations. The result- ing microstructures in CL can be basically distinguished in diffusion patterns (along microfractures and grain boundaries), and secondary quartz formed by dissolution-reprecipitation. Most of these textures are formed during retrograde fluid-controlled processes between ca. 220 and 500 ℃, i.e. the range of semi-brittle deformation (greenschist-facies) and can be correlated with the fluid inclusions. In this way modified and re-trapped fluids can be identified, even when there are no optical features observed under the microscope. 展开更多
关键词 Fluid inclusionsGranuliteCharnockiteCathodoluminescenceLA-ICPMSQuartz
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The significance of cherts as markers of Ocean Plate Stratigraphy and paleoenvironmental conditions:New insights from the Neoproterozoic-Cambrian Blovice accretionary wedge,Bohemian Massif 被引量:1
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作者 LukášAckerman Jirízák +5 位作者 Václav Kachlík Jan Pašava KarelZák Andreas Pack František Veselovsky Ladislav Strnad 《Geoscience Frontiers》 SCIE CAS CSCD 2023年第1期162-180,共19页
The Ediacaran to early Cambrian Blovice accretionary complex,Bohemian Massif,hosts abundant chert bodies that formed on an oceanic plate and were involved in subduction beneath the northern margin of Gondwana.Field re... The Ediacaran to early Cambrian Blovice accretionary complex,Bohemian Massif,hosts abundant chert bodies that formed on an oceanic plate and were involved in subduction beneath the northern margin of Gondwana.Field relationships of cherts to their host,their microstructure and elemental as well as isotopic compositions revealed diverse processes of chert petrogenesis reflecting depositional environment and position on the oceanic plate.The deep-water cherts formed through a hydrothermal precipitation of silica-rich gels on outer trench swell of the subducted slab with none or only minor addition of terrigenous material.On the contrary,the shallow-water cherts formed in lagoons on seamount slopes,and at least some of them represent a product of hydrothermal replacement of former carbonate and/or evaporite precursors.For both chert types,the hydrothermal fluids were of low temperature and continuous pervasive hydrothermal alteration of oceanic crust,together with an elevated Si content in Neoproterozoic seawater,served as the major source of silica.On the other hand,minor carbon enrichment in chert is mostly linked to variable incorporation of organic matter that was deposited on the seafloor.Rare earth element(REE)systematics of the cherts indicate predominantly oxygenated environment for the shallow-water cherts whereas the deep-water cherts were deposited in diverse redox conditions,depending on their distance from hydrothermal vent.Using these data,we demonstrate that the cherts once formed a part of Ocean Plate Stratigraphy(OPS)now dismembered and mixed with terrigenous siliciclastic material to form OPS mélanges.Combining our data with those from the existing literature,we show that cherts can serve as significant markers of OPS since the Archean,recording a complex interplay between seafloor-related volcanic(production of MORB-and OIB-like magmas)and sedimentary processes,hydrothermal activity at mid-ocean ridges and seamount chains as well as at outer slopes of subducting slabs.However,the cherts also exhibit a secular change in composition and petrogenesis most profoundly affected by an overturn in seawater silica cycle across the Precambrian-Phanerozoic boundary. 展开更多
关键词 Chert Accretionary wedge EDIACARAN Triple oxygen isotopes Strontium isotopes Ocean Plate Stratigraphy
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