Integrated biostratigraphy and carbon isotope stratigraphy of the Lower Cretaceous (Barremian to Albian) Adriatic-Dinaridic carbonate platform deposits in Istria, Croatia     

Blanka Cvetko Tešovi?  Bosiljka Glumac 《Cretaceous Research》2011,32(3):301-324

The Adriatic-Dinaridic carbonate platform (ADCP) was one of the largest and relatively well preserved Mesozoic platforms in the Mediterranean region (central Tethys). The peninsula Istria, in the northwestern part of the ADCP, is built up predominantly of shallow-water carbonates of the Middle Jurassic (Dogger) to Eocene age and, to a lesser extent, of Paleogene clastic deposits (flysch and calcareous breccia). This study focuses on a Lower Cretaceous (Barremian to Albian) succession of strata at five localities in western Istria. Stratigraphic determinations are based on identification of nine microfossil assemblages (benthic foraminifera and calcareous algae Dasycladales) and on using their taxa as index fossils. The age of strata with these microfossil assemblages, however, is questionable. Most of the age uncertainties are associated with a regional emersion, which occurred on the ADCP during the Aptian or close to the Aptian-Albian transition. It is unclear what portions of the Upper Aptian and/or Lower Albian are missing along this unconformity. A stable isotope study was conducted on homogenous micritic matrix samples in an attempt to resolve some of these uncertainties. Variations in carbon isotope compositions proved useful for stratigraphic correlation between the examined successions of strata, for improving their age determination, and for relating them to other coeval successions that span an important time interval of major oceanographic changes and carbon-cycle perturbations associated with the Early Aptian oceanic anoxic event (OAE 1a).  相似文献   

水中氯代烃单体碳同位素分析中预富集方法进展     

凌媛  黄毅  尚文郁  谢曼曼  刘舒波  孙青 《岩矿测试》2011,30(6):795-801

高精度准确测定氯代烃单体碳同位素对示踪污染物来源,了解污染物的生物降解过程具有重要意义。在环境转化过程中,有机污染物的同位素组成可能是稳定不变的,也有可能发生改变。若污染物的同位素组成在迁移转化过程中不变,根据其同位素组成可以示踪污染物的来源;若同位素组成变化,根据同位素分馏结果,可以评价环境中有机污染物降解发生的可能性和程度。本文综述了固相微萃取、静态顶空进样、吹扫-捕集、多级串联技术等前处理方法与气相色谱-燃烧-同位素比值质谱仪(GC-C-IRMS)联用分析水中氯代烃单体碳同位素的研究进展,比较了分析方法的优缺点。液-液萃取较少用于水中氯代烃的单体同位素分析。静态顶空进样、固相微萃取、吹扫-捕集都是无溶剂富集技术,与GC-C-IRMS联用分析水中氯代烃单体同位素过程中不存在或存在小且恒定的可校正的同位素分馏,分析精度一般优于1‰,没有二次污染,降低了杂质干扰,提高了GC-C-IRMS的分辨率和分析精度,降低了检测限。从静态顶空进样、固相微萃取、吹扫-捕集,到多级串联等技术与GC-C-IRMS联用分析水中氯代烃单体同位素比值,检测限逐渐降低。目前,吹扫-捕集-GC-C-IRMS在分析水中氯代烃中应用最广泛,重现性好、检测限低。针内微萃取、管内微萃取、搅动棒吸附萃取和顶空进样吸附萃取等前处理方法与GC-C-IRMS仪联用具有一定的应用前景。  相似文献   

高温熔融研制钾长石玻璃标准物质初探   总被引：1，自引：1，他引：0  

宋佳瑶  袁洪林  包志安  陈开运  贺国芬  范超 《岩矿测试》2011,30(4):406-411

激光剥蚀多接收等离子体质谱(LA-MC-ICPMS)是进行原位微区分析微量元素和同位素的重要技术之一,标准样品与样品之间的基体匹配是解决影响该技术准确分析的基体效应和分馏效应的首选方案。长石(特别是长石微区)的Pb同位素组成是示踪岩石形成和演化历史的重要途径,而LA-MC-ICPMS技术则是进行长石Pb同位素原位微区分析的关键技术,然而目前国内外尚没有合适的长石Pb同位素分析标准。文章研究探讨了利用高温炉进行原位微区分析钾长石中Pb同位素组成所用外部标准物质合成条件,结果表明,常规的74μm(200目)碎样无法得到均一的钾长石玻璃,需要将初始钾长石粉末研磨至1300目以下;高温炉合成温度为1680℃;熔融时间为2 h;采用液氮方式淬火。制成的钾长石玻璃除表面具有轻微的不均一性外,内部的Pb同位素比值为1.90779±0.00009(208Pb/206Pb,2s),0.75899±0.00004(207Pb/206Pb,2s),20.909±0.002(206Pb/204Pb,2s),15.871±0.002(207 Pb/204 Pb,2s)和39.888±0.005(208 Pb/204 Pb,2s),相应的相对标准偏差(RSD)分别为0.007%、0.008%、0.016%、0.016%和0.021%。表明利用本研究方法合成的钾长石玻璃可作为潜在的钾长石中Pb同位素组成原位微区分析外部校准物质。  相似文献   

黄土高原沟谷型滑坡整治研究——以延安市子长县阎家沟滑坡为例          下载免费PDF全文

张茂省  韩乾隆  黄玉华  胡炜 《水文地质工程地质》2011,38(2):135-138

以延安市子长县阎家沟滑坡为例,分析了沟谷型滑坡的发育特征和复活机理,认为沟谷型黄土滑坡再次产生失稳破坏的根本原因是水流不断冲刷侵蚀滑坡体,使滑坡前缘产生新的临空面,提出了基于"侧挡+排水"的整治措施,实现了低成本的沟谷型黄土滑坡的整治。  相似文献   

新疆阿克苏地区早寒武世碳酸盐岩沉积环境:微量元素和碳同位素证据   总被引：2，自引：0，他引：2  

姚春彦  马东升  丁海峰  张晓勇 《地球化学》2011,40(1):63-71

对出露于塔里木盆地北缘阿克苏地区寒武系纽芬兰统玉尔吐斯组上部和寒武系第二统肖尔布拉克组下部海相沉积碳酸盐岩进行了氧化-还原敏感元素(Mo、V、Cd和U)及稳定C、O同位素的地球化学剖面研究,以探讨早寒武世沉积碳酸盐岩的沉积环境.研究揭示,尤尔美那克剖面肖尔布拉克组底部和下部含有两个δ13C负异常,谷值分别为-2.1‰和...  相似文献   

滇西北衙金多金属矿床成矿地球化学特征   总被引：10，自引：0，他引：10  

肖晓牛 《地质与勘探》2011,47(2):170-179

北衙金多金属矿床是金沙江-哀牢山-红河断裂带与新生代富碱斑岩有关的斑岩型矿床之一.本文重点提供了流体包裹体中稀土微量元素和矿石S、Pb同位素分析结果,并对成矿流体及成矿物质来源等问题进行了讨论.研究表明,本区流体包裹体稀土总量较低,∑REE介于5.19×10-6～9.0×10-6之间,反映轻重稀土分馏程度的∑LREE/...  相似文献   

100MPa、800℃下Mo和W在流体／花岗质熔体相间分配的实验研究   总被引：3，自引：0，他引：3  

管申进  张辉  唐勇  张锦煦 《地球化学》2011,(6):516-524

利用“RQV-快速内冷淬火”（外加热冷封式）高温高压实验装置,在100MPa、800℃条件下,以东秦岭地区出露的高钾钙碱性岩浆岩（合峪花岗岩）为实验初始物,实验研究了Mo和W在花岗岩-H2O、花岗岩-NaCl（KCl）-H2O及花岗岩-NaF-H2O体系流体／熔体相间的分配行为。实验结果表明,Mo比W更倾向于分配进入流体相（DMo^流体/溶体〉〉DW^流体/溶体）,相对于纯水体系而言,流体介质中Cl和F的存在均有利于Mo和W向流体相迁移富集,随体系内Cl含量的不断增高,Mo和W的分配系数呈线性增大趋势,而在天然花岗岩可能含有的F含量范围之内,F含量的增高将阻碍Mo、W向流体相迁移,流体介质中Na／K（摩尔比）的变化对Mo和W的分配系数没有明显影响,表明体系碱质（Na或K）类型不是Mo和W在流体／熔体相间分配的主要影响因素。  相似文献   

四川盆地江油厚坝油砂有机地球化学特征与成因研究   总被引：5，自引：3，他引：2  

罗茂  耿安松  廖泽文  单玄龙 《地球化学》2011,40(3):280-288

四川江油厚坝油砂产出于侏罗系沙溪庙组下段,含油砂层沿北东方向延伸约25 km.露头和岩芯油砂样抽提得到氯仿沥青“A”含量为0.4％～33％.抽提物饱和烃GC-MS分析得到的分子有机地球化学特征表明,油砂油遭受严重生物降解,饱和烃分布呈现双大鼓包,正构烷烃和异构烷烃基木被降解;三环萜烷含量丰富,孕甾烷和升孕甾烷含最也较高...  相似文献   

浙江西部建德群锆石LA-ICP-MS之U-Pb同位素年龄及其地层学意义   总被引：2，自引：0，他引：2  

李祥辉  陈斯盾  罗家洪  王尹  曹珂  刘玲 《地质论评》2011,57(6)

利用LA-ICP-MS测试技术对浙西地区中生代晚期寿昌盆地典型剖面建德群9件凝灰岩和安山岩样品的锆石进行了同位素测年分析。结果显示:建德群锆石206Pb/238U年龄加权平均值范围在134～115Ma之间,属于早白垩世中—晚期;其所属的劳村组、黄尖组、寿昌组和横山组的锆石年龄分别是134～125Ma、125～118Ma、125～121Ma和121～115Ma,各自对应于欧特里夫期—巴雷姆期、阿普特期早—中期、阿普特期早期、阿普特期中期。由此认为,黄尖组的时代与寿昌组+横山组大致相当,前者与后两者横向可能为同时异相,并非上下关系;在寿昌和丽水两个盆地的寿昌组近乎同时,其上为时代大致相当的横山组与馆头组。  相似文献   

Determination of arsenic concentration and distribution in the Floridan Aquifer System     

T. Pichler  R. Price  O. Lazareva  A. Dippold 《Journal of Geochemical Exploration》2011,111(3):84-96

Here we report on the different sampling strategies for almost seven years of sampling rocks/sediments for the determination of As within the Intermediate Aquifer System (IAS) and upper Floridan Aquifer System (FAS), a very large and productive limestone aquifer spanning from Georgia into Florida. In the FAS, As contamination has become a recurring problem during aquifer storage and recovery (ASR), particularly in central and south Florida.To investigate these phenomena, samples from solid drill cores and rock cuttings were collected from the Hawthorn Group, Suwannee Limestone, Ocala Limestone and Avon Park Formation. Samples were taken along drill cores and rock cuttings (referred to as ‘interval’ samples) or from particular drill core sections and rock cuttings (referred to as ‘targeted’ samples) likely to contain elevated concentrations of As as indicated by the presence of pyrite, hydrous ferric oxide, organic matter, clay minerals, fracture surfaces, and high permeable (moldic) zones.Arsenic was present in all of the stratigraphic units at low concentrations, close to the global average for As in limestone of 2.6 mg/kg. The highest As concentration was 69 mg/kg. In all units, however, the average bulk As concentration in the targeted samples was substantially higher than that in the interval samples. Based on direct spot measurements by electron microprobe and indirect calculations, pyrite was identified as the main source of As in the FAS. Concentrations in pyrite ranged from less than 100 mg/kg to more than 11,000 mg/kg. Because pyrite is heterogeneously distributed, both vertically and horizontally in the sampled stratigraphic units, the same was observed for the distribution of As. However, As concentrations generally decreased with depth, i.e., highest As values in the Hawthorn Group and lowest As values in the Ocala Limestone and Avon Park Formation. Compared to pyrite, other trace minerals contained much less As.The average As concentrations of the two types of sample media (solid cores and rock cuttings) were quite similar. These results indicate that if simply the average bulk rock As concentration of a geologic unit is the desired outcome of an investigation, either interval or targeted sampling of rock cuttings, seems to be sufficient. This is particularly important when time and money are a factor. This approach could work equally well for any other trace element. Structural sedimentary information, such as fractures, etc., is likely lost, however, when sampling rock cuttings. Thus, if this information is required, solid core samples need to be collected by hollow core diamond drilling.  相似文献