新疆西天山智博铁矿岩浆-热液成矿作用—来自安山岩矿物学的证据

本文以智博铁矿区内的安山岩为研究对象,通过详细的野外地质调查,并利用电子显微镜和电子探针,对安山岩中的主要矿物进行了系统的岩相学观察和矿物学研究。研究表明,智博安山岩中斜长石主要为Na-高钠长石,具低TiO2,高Na2O和Al2O3的特点;辉石主要为普通辉石,具高TiO2,高Al2O3的特点;角闪石主要为镁角闪石和阳起石,具低TiO2和Al2O3,高MgO的特点;副矿物磁铁矿具高TiO2,低MgO和Al2O3的特点。辉石、角闪石矿物化学特征表明,智博铁矿安山岩的母岩浆属于壳幔混源的玄武质岩浆,构造环境为火山岛弧环境。智博安山岩中单斜辉石结晶温度为1225℃左右,结晶压力约0.795GPa,结晶深度约26km。智博铁矿后期的热液作用也参与了磁铁矿成矿,对智博铁矿的成矿有一定的贡献。     

江南造山带东段桃岭岩体的地球化学特征及其成因

位于江南造山带东段赣东北地区的桃岭岩体地球化学特征总体表现为高钾钙碱性系列,弱过铝质-强过铝质,高Mg#值。桃岭岩体富集轻稀土和大离子亲石元素,亏损高场强元素,具弱的Eu负异常(δEu=0.62~0.81)(样品TL-1除外δEu=0.47)。锆石LA—ICPMS U—Pb定年获得桃岭岩体的成岩年龄为早白垩世(140±1)Ma。岩体初始~(87)Sr/~(86)Sr为0.7131~0.7141,ε_(Nd)(t)值为-7.43~-6.71。结合前人研究,笔者认为早白垩世(约140 Ma)交代的地幔发生部分熔融,幔源岩浆底侵,使地壳深处(至少40 km)的变质沉积岩发生部分熔融,并且与少量的幔源岩浆发生了岩浆混合作用,形成了桃岭岩体。     

嵩山地区熊耳群火山岩岩石学、地球化学及成因探讨

近年在河南省嵩山地区发现有熊耳群火山岩地层。通过岩石学、地球化学特征及成因研究,认为嵩山地区熊耳群火山岩主要为弱过铝质流纹岩,属于高钾钙碱性系列-钾玄岩系列,以高硅、高钾、过铝、贫钠、贫钙镁为特征;轻稀土富集,重稀土亏损,轻重稀土分馏较为明显,Eu强烈负异常,Ce微弱负异常;富Ba而贫Sr,Rb,U,富Zr而贫Nb,Th,Hf,Ta;岩石属A型岩浆作用产物,形成于板内拉张环境。     

义敦岛弧带夏塞早白垩世A型花岗岩成因:锆石U-Pb年代学、地球化学及Hf同位素制约

义敦岛弧带晚中生代侵入岩体目前仍缺乏高精度的年代学数据制约,其成因也存在争论。作者首次在岛弧带中段夏塞银铅锌多金属矿区发现与成矿关系密切的黑云母二长花岗岩。本文对其开展了年代学、地球化学和Hf同位素分析,探讨成因及构造背景。LA-ICP-MS锆石U-Pb定年结果为103±1 Ma(MSWD=0.5),为早白垩世晚期岩浆活动产物。花岗岩属高钾钙碱性岩系,具有高硅、富碱和铁、贫钙和镁特征,Si O2含量为72.94%~74.98%,K2O+Na2O=7.56%~8.08%,铝饱和指数A/CNK=1.06~1.10,属弱过铝质岩石。岩石富集Zr、Hf等高场强元素和U、Th等大离子亲石元素,明显亏损Ba和Sr。REE具有明显的Eu负异常(δEu=0.13~0.25),总体呈较陡右倾的LREE富集和HREE相对亏损特征。岩相学和地球化学显示其为铝质A型花岗岩。Hf同位素组成εHf(t)=–2.7~0.6,二阶段模式年龄TDM2=925~1095 Ma。地球化学及Hf同位素揭示夏塞岩体为软流圈地幔与壳源长英质岩浆混合成因,并经历了斜长石、正长石和褐帘石等矿物的分离结晶。夏塞花岗岩体具有后碰撞花岗岩特征,形成于早白垩世晚期弧-陆碰撞造山后伸展构造背景。     

Trace element and Nd isotope analyses of apatite in granitoids and metamorphosed granitoids from the eastern Central Asian Orogenic Belt: Implications for petrogenesis and post-magmatic alteration

We present in situ trace element and Nd isotopic data of apatites from metamorphosed and metasomatized (i.e., altered) and unaltered granitoids in the Songnen and Jiamusi massifs in the eastern Central Asian Orogenic Belt, with the aim of fingerprinting granitoid petrogenesis, including both the magmatic and post-magmatic evolution processes. Apatites from altered granitoids (AG) and unaltered granitoids (UG) are characterized by distinct textures and geochemical compositions. Apatites from AG have irregular rim overgrowths and complex internal textures, along with low contents of rare earth elements (REEs), suggesting the re-precipitation of apatite during epidote crystallization and/or leaching of REEs from apatite by metasomatic fluids. ε_Nd(t) values of the these apatites are decoupled from zircon ε_Hf(t) values for most samples, which can be attributed to the higher mobility of Nd as compared to Sm in certain fluids. Apatites from UG are of igneous origin based on their homogeneous or concentric zoned textures and coupled Nd-Hf isotopic compositions. Trace element variations in igneous apatite are controlled primarily by the geochemical composition of the parental melt, fractional crystallization of other REE-bearing minerals, and changes in partition coefficients. Sr contents and Eu/Eu* values of apatites from UG correlate with whole-rock Sr and SiO₂ contents, highlighting the effects of plagioclase fractionation during magma evolution. Apatites from UG can be subdivided into four groups based on REE contents. Group 1 apatites have REE patterns similar to the host granitoids, but are slightly enriched in middle REEs, reflecting the influence of the parental melt composition and REE partitioning. Group 2 apatites exhibit strong light REE depletions, whereas Group 3 apatites are depleted in middle and heavy REEs, indicative of the crystallization of epidote-group minerals and hornblende before and/or during apatite crystallization, respectively. Group 4 apatites are depleted in heavy REEs, but enriched in Sr, which are features of adakites. Some unusual geochemical features of the apatites, including the REE patterns, Sr contents, Eu anomalies, and Nd isotopic compositions, indicate that inherited apatites are likely to retain the geochemical features of their parental magmas, and thus provide a record of small-scale crustal assimilation during magma evolution that is not evident from the whole-rock geochemistry.     

江西德兴斑岩铜矿石英闪长玢岩成因及成矿学意义

为探究石英闪长玢岩成因及幔源基性岩浆对斑岩铜矿的贡献,本文选取德兴矿床石英闪长玢岩开展了锆石U-Pb定年、Hf同位素和全岩地球化学研究。获得石英闪长玢岩LA-ICP-MS锆石U-Pb年龄为169 Ma,与成矿花岗闪长斑岩侵位时间一致,岩体为中侏罗世岩浆活动的产物。石英闪长玢岩具有低的SiO₂(58.41%~63.12%)和K₂O(1.68%~2.94%)含量及A/CNK值(0.85~1.04),富集大离子亲石元素和轻稀土元素,亏损高场强元素Nb、Ta、Ti和重稀土元素,属于钙碱性到高钾钙碱性系列岩石。具有相对亏损的锆石Hf同位素组成,εHf(t)=2.20~7.93(最大值7.93),指示其源区为岩石圈地幔。锆石稀土元素配分模式图显示出明显的正Ce异常,岩浆氧逸度(lg f_O2)为-20.05~-6.66,达到磁铁矿-赤铁矿氧逸度等级,指示石英闪长玢岩结晶自高氧逸度岩浆。全岩地球化学特征显示,德兴石英闪长玢岩与成矿花岗闪长斑岩及其暗色包体符合岩浆混合的演化趋势,说明成矿花岗闪长斑岩可能是中侏罗世幔源基性岩浆和地壳酸性岩浆大规模混合作用的产物,并且石英闪长玢岩代表了岩浆混合过程中的幔源基性端员。结合前人研究成果,认为在中侏罗世伸展构造背景下,软流圈物质上涌导致新元古代受交代的岩石圈地幔部分熔融形成幔源基性岩浆,基性岩浆的底侵作用诱发下地壳物质熔融并与之发生一定程度的岩浆混合作用,形成了花岗闪长斑岩的母岩浆。高氧逸度幔源岩浆的加入可抑制斑岩体系硫化物的过早饱和,同时为德兴矿床注入了成矿所需的部分挥发分和金属元素。     

Late Jurassic Volcanism Deduced from Geochemical,Geochronological, and Sr-Nd-Hf Isotopic Composition Characteristics of the Nanyuan Formation,South China

The Nanyuan Formation contains information related to the Mesozoic tectonic transformation. In this study, three representative profiles were surveyed from the Nanyuan Formation, and multiple analyses were conducted. Zircon U-Pb dating yielded their ages as approximately 158–146 Ma. The volcanic rocks are enriched in Rb, Th, U, K, and Pb and depleted in Nb, Ta, P, and Ti, implying their affinity for I-type granites. The ε_Nd(t) values(-8.3 to-6.0),(⁸⁷Sr/⁸⁶Sr)_...     

博格达造山带东段早石炭世火山岩地球化学特征及构造属性

博格达造山带东段克孜库都克地区七角井组玄武岩和中酸性火山碎屑岩及少量流纹岩在时空上构成双峰式火山岩组合。玄武岩LA-ICP-MS锆石U-Pb年龄为331.0±3.0Ma,属于早石炭世晚期;Si O2含量为47.68%~48.82%,Ti O2含量(1.83%~2.17%)略高于N型大洋中脊玄武岩,高Al(Al2O3含量为15.56%~16.09%),富钠贫钾(Na2O/K2O=5.44~7.76),低Mg(Mg O含量为5.97%~7.17%,Mg#为43~47),表明其原始岩浆发生过明显的橄榄石和辉石的分离结晶作用。玄武岩具有近于平坦的稀土配分模式,轻微负Eu异常(δEu=0.89~0.93),相对富集Rb、Ba、P,亏损Th、Nb、Ta、Sr、Ti等不相容元素。火山岩岩石地球化学特征表明:研究区玄武岩可能是亏损尖晶石相地幔橄榄岩向石榴石相地幔橄榄岩过渡的产物,且在其上升过程中受到较弱程度的地壳物质混染,形成于陆内裂谷环境,其地球动力学体制可能与古亚洲洋壳向先存的准噶尔-吐哈陆块斜向俯冲,产生的侧向撕裂力拉张陆块有关。克孜库都克地区早石炭世玄武岩构造属性的确立进一步证实了博格达造山带在石炭纪时期处于大陆裂谷演化过程的观点,为进一步深入理解博格达地区石炭纪构造岩浆演化过程提供了新的地质与年代学依据。     

雅鲁藏布缝合带巴尔蛇绿岩边部石英菱镁岩成因

石英(滑石)菱镁岩是基性岩、超基性岩与富CO2流体反应形成的一套硅化-碳酸盐化蚀变岩,常伴生金、汞、菱镁矿、碱金属矿化而在国外备受关注,但国内相关研究较薄弱。巴尔蛇绿岩位于西藏阿里地区,石英菱镁岩主要出露在蛇绿岩体东北边界,出露厚度约20 m,近北西西向延伸数千米。本文系统研究了雅鲁藏布缝合带西段巴尔蛇绿岩边部石英菱镁岩矿物学及地球化学特征。根据尖晶石镜下特征,划分为两个阶段:一阶段石英菱镁岩中尖晶石稳定存在,二阶段石英菱镁岩中尖晶石几乎全部蚀变(代表更强程度蚀变作用)。石英菱镁岩主要地球化学组成为Si O2、Mg O及CO2,8件样品主量元素含量变化较大,Si O2/Mg O比值波动较大,反映石英菱镁岩形成为非等化学过程。蛇纹石化橄榄岩与石英菱镁岩有着相似微量元素分布规律,表明同源性,但两者仍有较明显差异:两阶段石英菱镁岩LREE都较地幔橄榄岩略富集,从地幔橄榄岩到两阶段石英菱镁岩,HREE先亏损再略富集。微量元素标准化图解中,Sr在橄榄岩与石英菱镁岩中都为正异常,其含量随蚀变强度增强而增加。此外,两阶段石英菱镁岩均无Au、Hg矿化。     

滇西新街岩体LA-ICP-MS锆石U-Pb年龄、Hf同位素和地球化学及其构造意义

新街岩体位于昌宁-孟连带北段,主要岩性为二长花岗岩。LA-ICP-MS锆石U-Pb定年结果表明,新街岩体侵位于约82Ma。岩体Si O2含量为74.28%~75.17%,富钾(K2O/Na2O=1.44~1.73)和较低钙Ca O(0.37%~0.41%),铝饱和指数(A/CNK)为1.121~1.156,富集Rb、Th、K、LREE等元素,相对亏损Nb、Ta、Ti、Zr、Hf等高场强元素。这些特征表明,新街岩体属于强过铝质S型花岗岩。新街岩体负且变化范围大的锆石εHf(t)值(-16.9~-0.5)和古老的Hf同位素地壳模式年龄(1.19~2.28Ga),表明其主要来源于古老地壳物质的重熔,并有不同程度的幔源物质加入。由于喜马拉雅新特提斯洋封闭发生在65Ma左右,新街岩体很可能是在喜马拉雅新特提斯洋洋壳俯冲的地球动力学背景下形成的。