Structure of the Middle Urals,east of the main Uralian Fault     

M. Friberg  G. A. Petrov 《Geological Journal》1998,33(1):37-48

In the Middle Urals, volcanic-arc and back-arc basin rocks of Ordovician to Devonian age occur in the Tagil Synform. These outboard terranes were thrust westwards in the late Carboniferous onto continental margin associations of late Proterozoic and Palaeozoic age, now exposed in the Central Uralian Uplift. The Main Uralian Fault coincides approximately with the suture separating the outboard terranes from the East European Platform margin. New fieldwork in the hinterland of the Middle Urals in the area east of the Tagil Synform has found structural evidence favouring E-directed thrusting of accreted terranes and eugeoclinal allochthons in the late Palaeozoic. The upper tectonic units are composed of ophiolite mélange and volcano-sedimentary rocks of Ordovician to Devonian age; they are thrust onto high-grade gneisses, some of possible microcontinental affinities, extensively intruded by mid-Palaeozoic granitic plutons. The nappes in the hinterland are refolded by major upright antiforms and synforms that fold the entire tectonostratigraphy. After thrust assembly, all tectonic units east of the Main Uralian Fault were intruded by late Carboniferous to early Permian granites. Reflection seismic profiles (recorded to 8 s TWT), recently reprocessed at Cornell University, image the major fold structures and demonstrate that they are restricted to the upper crust, being underlain by an extensive zone of flat-lying middle crustal reflectivity. At 10–15 km depth the latter appears to truncate all structures, including the late- to post-tectonic granitoids and extensional faults, east of the Main Uralian Fault. Previous studies (potential-field, refraction- and wide-angle-reflection seismics) have identified an anomalously deep crust under the Tagil Synform and have concluded that the root zone of the orogen is located beneath this belt. The new evidence presented here supports this interpretation, with back-thrusting of the oceanic rocks eastwards over Palaeozoic accreted terranes. © 1998 John Wiley & Sons, Ltd.  相似文献   

阿拉斯加型岩体的基本特征、成岩过程及成矿作用   总被引：2，自引：2，他引：0  

崔梦萌  白洋  罗扬  苏本勋  肖燕  王静  潘旗旗  高东林 《矿床地质》2020,39(3):397-418

阿拉斯加型岩体是一类具有独特的岩性环带状结构的镁铁-超镁铁质侵入体,常呈链状分布于汇聚板块边缘。其形成时代跨度较大,从元古代到新生代均有分布,以中生代最为发育。大部分阿拉斯加型岩体规模较小,出露面积约12～14 km~2或更小,平面上呈近似同心环状结构,垂直剖面上呈管道状。岩体中心为纯橄岩,向外依次包括异剥橄榄岩、橄榄单斜辉石岩、单斜辉石岩、角闪单斜辉石岩、角闪石岩和辉长岩。造岩矿物为橄榄石、单斜辉石、角闪石等,副矿物为铬铁矿、磁铁矿、钛铁矿等,超镁铁质岩石中少或无斜方辉石,斜长石仅出现在边缘的辉长质岩石中。磁铁矿在单斜辉石岩和角闪石岩中为常见矿物,含量最高达15%～20%。阿拉斯加型岩体的主量元素成分揭示所有岩石均为与拉斑玄武质岩浆分异有关的亚碱性堆晶岩。微量元素成分上显示平坦的稀土元素配分型式和较低的微量元素含量,且富集大离子亲石元素,亏损高场强元素。矿物化学特征上,橄榄石富镁且Fo值变化较大;单斜辉石主要为富Ca的透辉石,其成分变化具有弧堆晶趋势;角闪石主要是镁角闪石和韭角闪石;铬铁矿富集Fe-Al,贫Cr。这些特征揭示,该类岩体成因明显不同于层状岩体和阿尔卑斯型岩体。综合岩石学、矿物学和地球化学分析表明,阿拉斯加型岩体形成于与板块俯冲作用有关的岛弧或者活动大陆边缘背景下,其母岩浆为受到熔/流体交代的地幔楔部分熔融产生的含水玄武质岩浆。各岩相为未受明显地壳混染的同源母岩浆在地壳深度结晶分异的产物。阿拉斯加型岩体的岩浆体系具有含水且高氧逸度的特征,其通常为铂族元素和铬铁矿矿床的重要载体,无或少铜镍矿化。  相似文献   

新疆西天山备战基性-超基性岩矿物地球化学研究及其对铁成矿作用的制约     

骆文娟  张作衡  段士刚  蒋宗胜  王大川  陈杰 《矿床地质》2020,39(3):419-437

文章对备战铁矿区内的基性-超基性岩、中基性岩脉、矿体围岩和铁矿石中的辉石、橄榄石、金云母、铁钛氧化物进行了电子探针分析与显微特征研究。金云母辉石橄榄岩中辉石的化学成分在w(SiO_2)-w(Al_2O_3)图中均落于亚碱性系列区域,在w(Al_2O_3)-w(Na_2O)-w(TiO_2)图中,辉石主要落在拉斑玄武岩系列区域,表明该区岩浆经历了拉斑玄武岩系列演化。备战金云母辉石橄榄岩中橄榄石的w(FeO)较低,介于19.22%～23.79%,w(MgO)较高,介于37.35%～41.30%,Fo变化介于0.74～0.79,属于贵橄榄石。橄榄石中较低的w(FeO)表明其形成于较高的氧逸度环境,而岩浆的拉斑玄武岩系列演化一般发生于低氧逸度条件,综合分析岩浆经历了从低氧逸度到高氧逸度变化的过程。随着岩浆的演化,橄榄石Fo与w(Ni)由负相关变为正相关又变为负相关关系,其中负相关关系表明在岩浆演化过程中橄榄石与粒间硫化物熔浆发生过Ni-Fe交换反应,从另一方面可以认为岩浆中含有丰富的硫,岩浆中的高硫特征很可能是备战磁铁矿为较纯磁铁矿(低Ti)的原因之一。此外,成矿岩浆具有高氧逸度特征,铁钛氧化物固溶体在亚固相条件下的氧化作用使固溶体发生分离以及铁磷络合物的发育等因素是造成矿区磁铁矿为较纯磁铁矿(成分接近分子式Fe_3O_4)的原因。金云母辉石橄榄岩和铁矿石中均发育金云母,表明铁矿与基性-超基性岩的源区都是富含挥发分的。该区铁钛氧化物主要有4种:较纯磁铁矿、含钛铬磁铁矿、铬铁矿、钛铁矿。金云母辉石橄榄岩中的较纯磁铁矿(低Ti),与铁矿石中磁铁矿成分类似,表明两者具有成因联系。结合金云母辉石橄榄岩的显微特征分析,在岩浆阶段曾有一期富铁镁岩浆的加入,这很可能为备战铁矿的形成提供了主要的铁质来源。  相似文献   

Apatite U–Pb geochronology and whole rock,Sr–Nd–Pb isotopic geochemistry of XV mafic-ultramafic intrusion,Bafq, Central Iran: Implications for petrogenesis and tectonic setting     

Sakine Amraei  Mohammad Yazdi  Liang Qiu  Chang-Zhi Wu  Lei Chen  Bertrand Moine  Majid Ghasemi Siani  Qihui Zhang  Shahrokh Rajabpour 《Island Arc》2024,33(1):e12514

The XV mafic-ultramafic intrusion is located in the western part of the Posht-e-Badam Block (PBB) within the Central Iranian Micro-Continent (CIMC). Petrographically, the intrusion is composed of gabbro and pyroxenite. Apatite U–Pb dating has established the crystallization age of this intrusion to be 363 ± 67 Ma. The XV intrusive rocks are tholeiitic to slightly calc-alkaline in nature and are characterized by an enrichment of large ion lithophile elements (LILE) and light rare earth elements (LREE) relative to high field strength elements (HFSE) and Heavy Rare Earth Elements (HREE), respectively. The major oxide elements display continuous trends relative to SiO₂. The ⁸⁷Sr/⁸⁶Sr(i) ratios range from 0.7045 to 0.7056, and the εNd(i) values range from 2.63 to 3.30. In addition, the ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb, and ²⁰⁸Pb/²⁰⁴Pb ratios exhibit a narrow range, varying from 18.68 to 18.70, 15.67 to 15.71, and 38.84 to 38.99, respectively. The geochemical and isotopic characteristics suggest that the parental magma was derived from a Sub- Continental Lithospheric Mantle (SCLM) that was modified by oceanic slab-derived components. The locations of the XV intrusive rocks in εNd(i) versus TDM (Ga) and Nb/La versus discrimination diagrams further support this conclusion. Fractional crystallization is identified as the dominant process influencing the formation of distinct lithological units within the XV intrusive rocks. Our newly presented isotopic and geochronological data, when considered in the regional context, suggest that the XV intrusive rocks were formed in an extensional tectonic setting. In this scenario, upwelling from the asthenospheric mantle induced heating, leading to the melting of previously subduction-modified SCLM. Comparative analysis with previously published ages indicates that extensional magmatism in the PBB continued into the Middle Paleozoic.  相似文献   

壳聚糖硫酸酯金属配合物的抗氧化活性   总被引：1，自引：0，他引：1       下载免费PDF全文

刘松  邢荣娥  蔡圣宝  于华华  李鹏程 《海洋科学》2009,33(11):11-14

以吩嗪硫酸甲酯-NADH为超氧阴离子自由基(O_2~(·-))产生、检测体系和EDTANa_2-Fe(Ⅱ)-H_2O_2为羟自由基(~·OH)产生、检测体系,对壳聚糖硫酸酯铜、锌配合物和不同分子质量壳聚糖进行了抗O_2~(·-)和~·OH自由基的活性研究.结果表明,壳聚糖硫酸酯金属配合物对于O_2~(·-)自由基的清除能力明显高于壳聚糖,在质量浓度为0.025 g/L时,壳聚糖硫酸酯铜配合物对O_2~(·-)自由基的清除能力达到94.18%,壳聚糖硫酸酯锌配合物达到93.19%;壳聚糖硫酸酯铜、锌配合物对~·OH自由基的清除能力(67.39%、60.46%)低于相同分子质量的壳聚糖(88.06%),而高于高分子质量壳聚糖761 ku(18.71%);壳聚糖分子质量大小对O_2~(·-)和~·OH自由基的清除能力有较大影响,质量浓度为1.6 g/L壳聚糖分子质量为20 ku时,对O_2~(·-)清除率达54.69%,而分子质量在761 ku时,对O_2~(·-)清除率仅为35.50%;各样品对O_2~(·-)和~·OH自由基的清除能力均随着质量浓度的增加而上升,壳聚糖硫酸酯铜、锌配合物在相当低的浓度下(0.025 g/L)就可以达到明显清除O_2~(·-)自由基的效果(≥90%).  相似文献