独居石矿物地球化学对南秦岭宁陕地区Be- Nb伟晶岩成因的指示

近年来,在秦岭造山带宁陕伟晶岩区发现了数条Be-Nb稀有金属伟晶岩矿脉。本文通过扫描电镜和电子探针分析了Be-Nb伟晶岩中独居石的矿物学特征和矿物成分。研究结果表明,伟晶岩脉中的独居石可分为两类:Ⅰ类独居石主要分布在石英、长石等造岩矿物内部,在背散射图像中多数Ⅰ类独居石内部均匀,部分可见振荡环带,具有较高的Th O₂含量(7.0%～13.9%,平均10.5%);Ⅱ类独居石单矿物在背散射图像下同样显示内部均匀,但亮度明显低于Ⅰ类独居石,且Th O₂含量较低(0.9%～4.4%,平均2.2%)。这指示了Ⅰ类独居石的岩浆成因和Ⅱ类独居石的热液成因。岩浆成因独居石具有较高的Th O₂含量与独居石中磷钙钍石的类质同象替代密切相关。岩浆成因独居石的U-Pb测年结果为200.8±2.1 Ma,代表伟晶岩的成岩年龄,该年龄结果接近宁陕岩基中的二长花岗岩。岩浆和热液成因独居石的εNd值的范围为4.6～3.0,这与二长花岗岩的εNd值范围基本一致,说明区内Be-Nb伟晶岩与上述二长花岗岩的同源性。综上所述,本研究认为宁陕地区Be-Nb伟晶岩...     

独居石成因特征与U-Th-Pb定年及三江特提斯构造演化研究例析

独居石U-Th-Pb定年在地质年代学研究中占有重要地位,但其成因类型的识别和年龄值的合理地质解释始终是研究的难点。论文通过对比分析岩浆、热液和沉积成因独居石的内部结构、矿物组合以及稀土和微量元素地球化学特征,厘定了不同成因类型独居石的鉴别标志;并以三江特提斯构造演化研究为例,探讨了独居石的U-Th-Pb定年及其合理地质应用。不同地质环境中形成的独居石具有不同的内部结构和矿物组合及元素组成:岩浆独居石可能存在较宽且平直的岩浆环带,常与磷钙钍石共生;相对富集重稀土,具有较高的Y、Sc、Th、U、Sm、Gd等含量和Th/U比值,较低的La、Ce含量和稀土总量,显示为Eu强烈亏损的右倾斜分布模式。而热液独居石可能存在与流体作用有关的扇形环带,常与斜钍石共生;沉积独居石形态多不规则,与自生矿物相伴生。它们具有典型的四分组稀土分布模式,稀土总量较高,相对富集轻稀土(如La、Ce),贫Y、Sc、Th、U、Sm、Gd等,Th/U比值较低。独居石U-Th-Pb定年限定了松潘-甘孜造山带204~190Ma的早期变质作用和168~158Ma的局部热干扰,约140~130Ma冈底斯浅色花岗岩的形成与地壳的缩短加厚及快速隆升作用,约33~22Ma 红河断裂带与伸展作用有关的岩体侵位和左行走滑运动年代(且北部的去顶剥蚀作用要比中部早9Ma),约8~11Myr的东喜马拉雅构造结"挤出"构造变形时限。     

贵州遵义镍-钼富集层中独居石的发现及成因意义

对贵州遵义天鹅山-黄家湾镍-钼富集层中镍-钼矿石进行了电子探针研究,在镍-钼矿石中发现了稀土独立矿物——独居石,呈不规则的细粒、蠕虫状分布于矿石中,并与镍、钼的独立矿物共生;独居石La和Ce的含量高(La2O3含量变化范围为25.70%～30.52%,Ce2O3含量变化范围为22.96%～27.68%),贫Sm、Th(Sm2O3含量的变化范围为0.49%～0.80%,ThO2含量的变化范围为0%～0.19%),具有热液成因独居石的化学成分特征。镍-钼矿石中稀土矿物独居石的发现为镍-钼矿层的热液成因提供了直接的矿物学证据。     

新疆拜城波孜果尔碱性岩中副矿物的特征

在野外地质调查的基础上,结合室内显微镜观察及电子探针分析测试,对新疆拜城波孜果尔碱性岩中的副矿物的矿物学特征和化学成分进行了研究.发现这些副矿物常以共生组合的形式产在碱性岩中,主要分布在石英二长闪长岩和石英二长岩中.烧绿石中U、Th和REE替代Ca、Na.独居石富含LREE,Th和LREE相互替代;根据独居石中w(La+ Ce) ＞40％和La/Nd比值在1.6～4.5,推断独居石为热液成因.磷钇矿中富含REE,且以HREE为主;w(Th)＞w(U).锆石中Zr/Hf比值在60％以上,符合碱性岩特征;其Th/U比值为0.6,属于岩浆锆石.星叶石中w(Rb2O)、w(Cs2O)较高.萤石中Y、Ce替代Ca.锆石中的钍石w(U)明显高于磁铁矿中钍石w(U).在石英二长岩中,烧绿石的w(CaO)、w(TiO2)、w(ZrO2)、w(U3O8),磷钇矿的w(Y2O3),星叶石的w(TiO2),萤石的w(Ca),氟碳铈镧矿的w(CaO)较丰富;而在石英二长闪长岩中,烧绿石的w(Ce2O3),磷钇矿的REE含量,星叶石的w(Nb2O5)、w(Rb2O),萤石w(Ce)、w(Y)和氟碳铈镧矿的w(La2O3)较高.     

不同成因锆石阴极发光及微量元素特征:以新疆阿尔泰地区花岗岩和伟晶岩为例

新疆阿勒泰可可托海地区出露大量花岗岩和伟晶岩脉,利用阴极发光显微照相(CL)、电子探针背散射(BSE)和激光剥蚀电感耦合等离子质谱技术(LA-ICP-MS),观察和分析岩石中锆石的内部结构、稀土元素及Th,U含量后结果表明:该区花岗岩锆石具振荡环带和强烈的阴极发光特征,Th/U比值较高(Th/U=0.16～0.99),轻稀土亏损、重稀土富集,具较大的Ce正异常,为典型岩浆成因锆石。伟晶岩(KP-08-11)锆石为热液锆石,不具振荡环带和阴极发光,具低的Th/U比值(0.01～0.13),强烈富集稀土元素,尤其是轻稀土元素较花岗岩锆石高一个数量级,Ce的正异常相对较低。伟晶岩(KP3-08-1)锆石为变质重结晶锆石,Th/U比值分布范围较广(0.01～0.78),强烈亏损稀土元素,稀土元素配分模式存在显著的"REE四分组效应"。微量元素特征表明,伟晶岩(KP-08-11)锆石可能结晶自富U贫Th的残余岩浆流体,而伟晶岩(KP3-08-1)的锆石经历了蜕晶质化和变质重结晶作用,但依然保持了共存伟晶岩熔体的微量元素特征。     

可尔因稀有金属矿床液态不混溶作用的地球化学特征证据

可尔因稀有金属矿床位于松潘-甘孜造山带东部,是川西地区发现的巨型伟晶岩型稀有金属矿床;矿体主要赋存于钠长石锂辉石型伟晶岩中,围绕可尔因岩体成群成带分布。矿床地球化学特征研究表明,碳、氢-氧同位素和锶同位素特征显示成矿流体来源于壳源岩浆。二云母花岗岩与伟晶岩间相似的地球化学特征表明,两者均属于地壳重熔成因,含矿伟晶岩中的成矿物质来源于二云母花岗岩;二云母花岗岩与伟晶岩间存在Al_2O_3、Na_2O和Si_2O,K_2O相分离的现象;从二云母花岗岩至伟晶岩Li、Be、Nb、Ta等稀有元素,F、B等挥发分含量,∑REE、∑Ce/∑Y、(La/Yb)n、(Gd/Yb)n、δEu等具有突变现象;所有这些特征表明伟晶岩可能是由二云母花岗岩岩浆液态不混溶分异结晶形成,岩浆演化过程中,轻重稀土的分异导致稀有元素越来越富集,最终在远离岩体的部位形成富含稀有金属的伟晶岩和矿体。     

内蒙古大石寨地区稀土元素的区域分布特征

总结了内蒙古大石寨地区1∶25万区域地球化学调查获得的1点/4km2的水系沉积物组合样品中的La、Ce、Pr、Nd、Sm、Eu、Gd、Tb、Dy、Ho、Er、Tm、Yb、Lu、Y等15种稀土元素的区域地球化学分布特征。稀土元素分布与研究区中部的黑云母花岗岩密切相关,轻稀土主要分布在该岩体外围的二叠系地层中,重稀土主要分布在该岩体上方。该岩体上方和外围地层的稀土元素分布、稀土元素总量、轻重稀土比及δCe、δEu、(La/Sm)N、(La/Tb)N、(La/Lu)N、(Ce/Yb)N、(Gd/Lu)N等稀土元素分馏特征的差异明显。利用区域地球化学调查水系沉积物样品中的稀土元素含量,可获得研究区可靠的稀土元素区域地球化学分布特征,也可反映研究区地质特点,并为区域地球化学异常解译提供参考资料。     

白云鄂博西矿区伴生型萤石矿床的稀土元素地球化学特征及其指示意义

内蒙古白云鄂博伴生型萤石矿床是举世瞩目的超大型矿床,但萤石成因目前仍然存在争议。本文在系统研究白云鄂博西矿区地质特征及含萤石矿石分布规律的基础上,针对萤石矿石与赋矿H8白云岩开展了主量、微量、稀土元素地球化学研究。结果表明:西矿区萤石属于白云石型矿石,萤石和白云岩的稀土元素特征均为轻稀土元素相对富集,重稀土元素相对亏损,萤石和白云岩稀土元素配分曲线具有相似性;所有样品均表现出Ba、Th、Sm、Ce的含量相对较高,特别是Ba、Th的含量明显偏高,矿区萤石单矿物δEu值为0.93~1.14,既有正异常又有负异常,δCe值为1.15~2.11,平均1.51,表现为Ce的正异常。综合研究区萤石矿床地质、微量、稀土元素特征和(Y＋La)-Y/La、Y/Ho-La/Ho、Tb/Ca-Tb/La关系图,结合前人对萤石成矿流体的研究结果,认为白云鄂博西矿区伴生型萤石矿属于中高温热液交代型矿床,矿床成因与我国典型沉积改造型、热液填充型萤石矿床不同,与侵入花岗岩无关,主要成矿物质F和Ca元素源自加里东期钙质碳酸岩岩浆衍生的中高温流体对早期白云岩的交代作用。     

甘肃龙首山芨岭铀矿区A型似斑状花岗岩地质特征及其地质意义

似斑状花岗岩是芨岭岩体重要的侵入单元,研究其特征可为钠交代型铀矿化的成因机制研究提供依据。本文通过对芨岭铀矿区外围似斑状花岗岩的岩石学、同位素年代学、地球化学研究,认为其具有低硅、富铝、贫铁和镁、低钙和较高TFe O/Mg O值的岩石化学特征,其轻稀土分馏强烈、重稀土分馏较弱,具铕中等负异常,相对富集Rb、Th、U、La、Ce、Hf、Sm、Gd,而相对亏损Ba、Nb、Ta、Sr、Ti等元素,且(Zr+Nb+Ce+Y)含量和Ga/Al值明显高于Ⅰ型和S型花岗岩均值。上述地球化学特征表明它是铝质A型花岗岩,说明早古生代(458.3±2.3Ma)祁连山-龙首山造山作用已进入晚期的后碰撞伸展环境。芨岭铝质A型似斑状花岗岩既是钠交代型铀矿的主要铀源,又为矿体定位提供充足的容矿空间。     

锆石微量元素示踪锂成矿岩浆-热液演化过程

锂成矿过程中的岩浆- 热液演化过程目前仍不清楚。锆石作为花岗岩和伟晶岩中普遍存在的副矿物,其微量元素成分演化可以记录岩浆演化过程。本文以松潘- 甘孜构造带可尔因地区的花岗岩和伟晶岩中的锆石作为研究对象,对其进行原位微量元素分析。锆石的形态结构特征显示花岗闪长岩与花岗岩中的锆石为岩浆锆石,而伟晶岩中的锆石受到不同程度热液作用影响。元素分析结果显示,从太阳河花岗闪长岩到可尔因二云母花岗岩到无锂辉石伟晶岩到锂辉石伟晶岩,锆石中的稀有金属元素(Li、Sn、Nb、Ta和Hf)和U含量逐渐升高,锆石的Zr/Hf比值逐渐降低。除此之外,太阳河花岗闪长岩和可尔因二云母花岗岩中的锆石具有较低的Fe含量,而无锂辉石伟晶岩和锂辉石伟晶岩中的锆石具有明显升高的Fe含量,且锆石Fe含量与稀有金属元素含量具有正相关关系,反映出热液作用越强,稀有金属含量越高的特征。热液导致伟晶岩中锆石的U- Pb体系受到改造,使得获得的年龄不可靠,而伟晶岩铌钽矿U- Pb年龄(210 Ma)相对可靠。基于锆石的微量元素特征,我们认为太阳河花岗闪长岩与锂成矿伟晶岩没有成因联系,二云母花岗岩与锂成矿伟晶岩具有成因联系,但是二云母花岗岩不是成矿伟晶岩的直接母岩。二云母花岗岩和无锂辉石伟晶岩Li锆石/Li全岩接近甚至超过1,指示其与全岩成分不平衡,表明岩浆演化过程中曾形成富锂熔体,且富锂熔体的形成与液态不混溶作用无关,而是岩浆分异的结果。富锂熔体可能在区域拆离断层作用下从岩浆体系中分离,随后不断演化形成了锂辉石伟晶岩,而残余岩浆逐渐冷却结晶形成了二云母花岗岩和无锂辉石伟晶岩。基于锆石中的微量元素可以有效示踪锂成矿过程,并且利用碎屑锆石的微量元素特征还可以指示区域富锂岩浆的存在及其形成时代,有望成为示踪区域锂成矿的一种新方法。     

Zoning and sectoriality of monazite-(Ce) from granite pegmatites of the central and South Urals

Zonal and sectorial monazite-(Ce) crystals from ceramic granite pegmatites of the Adui pluton are enriched in Ce and La, whereas monazite from the miarolitic gemstone pegmatites at the western contact of the pluton are enriched in Nd, Sm, Gd, and Y. This difference is caused by earlier crystallization of ceramic pegmatites and higher temperatures of their formation (650–600°C for ceramic pegmatites and 550–300°C for miarolitic pegmatites). Monazites from ceramic and miarolitic pegmatites of the Adui pluton differ in La and Nd contents, but their compositional trend in La-Nd coordinates is similar to the variation in monazite composition from the early to late granite pegmatites in the Ilmeny Mountains. It is suggested that decrease in temperature is a factor controlling REE contents in monazite. Heterovalent P ↔ Si and REE ↔ Th, Ca isomorphism in the consecutive zones of growth pyramids in monazite is both unidirectional and wave-like. Monazite from granite pegmatites of the Adui pluton and Ilmeny Mountains crystallized mainly under slightly alkaline conditions.     

前寒武纪沉积岩中自生独居石的发现及其意义

由于受到葛家屯组中发现自生方铅矿的启发 ,首次于大连前寒武纪震旦系十三里台组泥岩中发现了自生独居石 ,这一发现为在中国北方前寒武纪沉积岩中寻找自生独居石提供了重要的线索。它为进一步探索 U、Th- Pb同位素测年拓展了新的研究领域和提供了可能性。本文列举了中国北方前寒武纪沉积岩中 Ce元素异常以及 REE较高的例证 ,认为上述地区都有可能发现自生独居石。同时介绍了最近又在北京十三陵中元古代的常州沟组和串岭沟组所发现自生独居石的新资料。研究表明 ,自生独居石的电子探针扫描形态 ,与岩浆岩、变质岩及砂矿中截然不同。在地质年代分布上 ,元古宙 REE相对丰度较高 ,特别是 L REE较高的泥质岩多数来自古陆壳上。资料对比结果显示 :在 L a+Ce+Nd、Yb+Y、Sm+Gd+Dy三角图中 ,北京十三陵元古宙泥质岩、大连震旦系十三里台组泥岩和辽南 -辽西中元古代泥质岩都属于近古陆的沉积类型。首次提出 ,中国北方元古宙沉积与南方震旦系磷块岩沉积环境存在明显的不同并反映在三角图中 ,前者离 L a+Ce+Nd端点近 ,而后者由于成因上属于洋流上升沉积物而远离该端点。按照大连震旦系十三里台组沉积环境特点 ,自生独居石应为生物成矿作用的产物 ,含矿物泥岩形成于总体氧化环境中的局部还原亚环境中。基于此 ,建立了     

阿尔泰喀纳斯早泥盆纪钾质富镁英安岩：俯冲沉积物熔体交代

阿尔泰造山带喀纳斯地区出露一套钾质富镁英安岩,锆石U Pb定年显示其形成于早泥盆世（411±4 Ma）。该套英安岩富SiO2（6471～6777 wt％）,MgO（328～353 wt％）和K2O（212～275 wt％）,贫Na2O（170～185 wt％）,K2O/Na2O比值介于（120～153）,具较高的Al2O3（1412～1533 wt％）和较低的CaO（112～128 wt％）,ASI指数>18,显示过铝质钙碱性岩浆系列特征,明显不同于初始的高镁安山质岩浆。样品具有中等的Cr（134×10-6～153×10-6）、Co（1747×10-6～1865×10-6）、Ni（71.64×10-6～80.76×10-6）含量,富集大离子亲石元素Rb、K和高场强元素U、Th、Pb及LREE,发育Sr、Ba及“TNT”（Ta、Nb、Ti）负异常,显示俯冲带岩浆岩地球化学特征。其高的Mg#（5171～5247）和低的εNd(t)值（-46～-42）说明该套火山岩可能来自遭受强烈交代作用的地幔楔部分熔融。样品具有较高的Ba/La、Pb/La比值和较低的Th/Yb、Nb/Y比值,显示地幔交代作用以俯冲沉积物熔体的交代作用为主。以上地球化学特征说明,喀纳斯钾质富镁英安岩可能主要是受俯冲沉积物熔体交代的上覆地幔橄榄岩部分熔融的产物,阿尔泰泥盆纪处于俯冲作用相关的活动大陆边缘构造环境。此外,该套火山岩的形成时代制约了其下覆的哈巴河群沉积上限,显示哈巴河群沉积于早泥盆世之前。     

赣东北地区不同时代硅质岩的地球化学特征及其地质意义

赣东北地区硅质岩各时代均有不同程度的发育,各时代硅质岩的SiO2含量变化范围为74．90％～97．19％,Si／Al为10．84～93．21,与Al2O3呈较好的负相关关系,表明它们含有较高比例的陆源泥质沉积物,硅质岩样品的Al2O3／(Al2O3+F2O3)=0．60～0．99,Ce／Ce=0．99～1．22,(La／Ce)N=0．91～1．83,V／Y<5．78,Ti／V>17。上述特征表明本区硅质岩形成于大陆边缘构造环境,而与大洋盆地及洋中脊构造环境无关。自古生代以来,该地区没有出现深海大洋盆地环境。     

REE partitioning between monazite and garnet: Implications for petrochronology

Rare‐earth element and Y partitioning between garnet and monazite was measured in metamorphic rocks from western Norway to provide more confidence in tying monazite U/Th–Pb dates to P–T conditions recorded in garnet. A subset of samples has low‐Y garnet mantles and low‐Y monazite cores that gave Y‐partitioning temperatures similar to independently determined metamorphic temperatures. In combination with previously published data, these monazite–garnet pairs have temperature‐dependent partitioning of the HREE from Dy to Lu, and nonsystematic partitioning of the LREE from La–Gd. The temperature‐dependent partitioning must be considered when using HREE to assess which portions of garnet and monazite might have coexisted, but experiments are needed to place the dependence on a firm footing.     

Monazite–xenotime miscibility gap thermometry. I. An empirical calibration

Rare earth element (REE) and yttrium concentrations of coexisting monazite and xenotime were determined from a suite of seven metapelites from the Variscan fold belt in NE Bavaria, Germany. The metapelites include a continuous prograde, mainly low-P (3–5 kbar) metamorphic profile from greenschist (c. 400 °C) to lower granulite facies conditions (c. 700 °C). The LREE (La–Sm) are incorporated preferentially in monoclinic monazite (REO₉ polyhedron), whereas the HREE plus Y are concentrated in tetragonal xenotime (REO₈ polyhedron). The major element concentrations of both phases in all rocks are very similar and do not depend on metamorphic grade. Monazite consists mainly of La, Ce and Nd (La_0.20–0.23, Ce_0.41–0.45, Nd_0.15–0.18)PO₄, all other elements are below 6 mol%. Likewise, xenotime consists mainly of YPO₄ with some Dy and Gd solid solutions (Y_0.76–0.80, Dy_0.05–0.07, Gd_0.04–0.06). In contrast, the minor HREE concentrations in monazite increase strongly with increasing metamorphic grade: Y, Dy and Gd increase by a factor of 3–5 from greenschist to granulite facies rocks. Monazite crystals often show zonation with cores low in HREE and rims high in HREE that is interpreted as growth zonation attained during prograde metamorphism. Similarly, Sm and Nd in xenotimes increase by a factor of 3–4 with increasing metamorphic grade. Prograde zonation in single crystals of xenotime was not observed. The X_HREE+Y in monazite and X_LREE in xenotime of the seven rocks define two limbs along the strongly asymmetric miscibility gap from c. 400 °C to 700 °C. The empirical calibration of the monazite miscibility gap limb coexisting with xenotime is appropriate for geothermometry. Due to its contents of U and Th, monazite has often been used for U–Pb age determination. The combination of our empirical thermometer on prograde zoned monazite along with possible age determination of zoned single crystals may provide information about prograde branches of temperature–time paths.     

Prograde metamorphic sequence of REE minerals in pelitic rocks of the Central Alps: implications for allanite–monazite–xenotime phase relations from 250 to 610 °C

The distribution of REE minerals in metasedimentary rocks was investigated to gain insight into the stability of allanite, monazite and xenotime in metapelites. Samples were collected in the central Swiss Alps, along a well‐established metamorphic field gradient that record conditions from very low grade metamorphism (250 °C) to the lower amphibolite facies (～600 °C). In the Alpine metapelites investigated, mass balance calculations show that LREE are mainly transferred between monazite and allanite during the course of prograde metamorphism. At very low grade metamorphism, detrital monazite grains (mostly Variscan in age) have two distinct populations in terms of LREE and MREE compositions. Newly formed monazite crystallized during low‐grade metamorphism (<440 °C); these are enriched in La, but depleted in Th and Y, compared with inherited grains. Upon the appearance of chloritoid (～440–450 °C, thermometry based on chlorite–choritoid and carbonaceous material), monazite is consumed, and MREE and LREE are taken up preferentially in two distinct zones of allanite distinguishable by EMPA and X‐ray mapping. Prior to garnet growth, allanite acquires two growth zones of clinozoisite: a first one rich in HREE + Y and a second one containing low REE contents. Following garnet growth, close to the chloritoid–out zone boundary (～556–580 °C, based on phase equilibrium calculations), allanite and its rims are partially to totally replaced by monazite and xenotime, both associated with plagioclase (± biotite ± staurolite ± kyanite ± quartz). In these samples, epidote relics are located in the matrix or as inclusions in garnet, and these preserve their characteristic chemical and textural growth zoning, indicating that they did not experience re‐equilibration following their prograde formation. Hence, the partial breakdown of allanite to monazite offers the attractive possibility to obtain in situ ages, representing two distinct crystallization stages. In addition, the complex REE + Y and Th zoning pattern of allanite and monazite are essential monitors of crystallization conditions at relatively low metamorphic grade.     

Monazite as an indicator of formation conditions of quartz veins at the Zhelannoe deposit,the Subpolar Urals

At the Zhelannoe quartz deposit, the content of monazite attains 0.5 wt % in unaltered sericitolite and 18 wt % in hydrothermally altered sericitolite. Two monazite generations, including four varieties, characterize the sequence of formation and alteration of sericitolite bodies at the Zhelannoe deposit. Monazite of the first generation occurs in unaltered sericitolite as prismatic and tabular crystals characterized by (Nd,Ce) > La and enrichment in HREEs and ThO₂ (5–16 wt %). Its formation is accompanied crystallization of milk white quartz. Monazite of the second generation occurs in altered sericitolite as the product of recrystallization of the first-generation monazite. The large drusy crystals of second-generation monazite were formed similarly with Alpine-type veins. Monazite of the second generation is characterized by Ce > (La,Nd), low contents of HREEs and ThO₂ (0.5–7 wt %) and high contents of CaO and SO₃ (up to 3–5 wt %). Monazite of the second generation appeared as a result of local superimposed processes and is a characteristic feature of the Zhelannoe deposit.     

冀北赤城红旗营子群黑云斜长片麻岩的岩石学、地球化学及原岩特征

冀北赤城红旗营子群黑云斜长片麻岩具斑状变晶结构,变基质为中、细粒鳞片粒状变晶结构,片麻状构造,局部保留有变余砂状结构。岩石主要由斜长石(28%~32%)、石英(35%~40%)、黑云母(18%~25%)及少量石榴石(2%~8%)和石墨(1%~4%)等组成,其变质演化可能是一个降温、降压的过程。黑云斜长片麻岩样品具有较宽的常量元素变化范围,稀土元素含量不是很高且变化较大,ΣREE介于49.45×10-6~140.10×10-6之间,具有轻稀土富集、重稀土平坦的球粒陨石标准化稀土配分模式,轻、重稀土元素比值为5.23~9.16,(La/Yb)CN值为5.07~8.70。大多数样品具中等程度的负Eu异常和不太明显的负Ce异常,(Eu/Eu*)CN和(Ce/Ce*)CN值分别为0.63~0.81和0.82~1.01。岩石中Rb、Sr、Cs、Ba、Zr、Hf、Nb、Ta、Th和U等微量元素含量均低于上地壳的平均含量,但Sr/Ba和Th/U值高于上地壳的平均值。红旗营子群黑云斜长片麻岩的地球化学特征表明其原岩应为泥质(或含泥质)砂岩,可能形成于大陆岛弧环境。     

准噶尔盆地西北缘晚石炭系-早二叠系火山岩岩石学和地球化学研究

晚石炭纪-早二叠纪,在准噶尔盆地西北缘,发育区域性的火山岩建造,岩性以酸性英安岩和流纹岩为主,同时发育少量中性玄武安山岩和安山岩,多属于中-低钾的钙碱性系列。样品全碱(Na₂O+K₂O)含量为0.99％ ～8.12％,K₂O的含量较低,为3.01％ ～0.05％,稀土元素总量(∑ REE)较低。稀土元素轻重分异,轻稀土元素(LREE)相对于重稀土元素(HREE)富集:(La/Yb)_N=0.76～5.18,且部分样品显示轻微的Eu负异常和Ce正异常:δEu=0.533～1.148,δCe=0.979～1.224。微量元素中大离子亲石元素(LILE)富集,高场强元素Nb、Ta亏损。分析认为石炭系末期-二叠系早期,研究区所处构造环境为洋内弧附近的前弧盆地,发育的火山岩是母源岩浆经历了一定程度分异作用后的产物,以岛弧环境为主,兼具有部分板内大陆环境特征。