东疆白石头泉含黄玉天河石花岗岩体的地球化学：分带和岩浆演化   总被引：2，自引：0，他引：2  

顾连兴  吴昌志  张遵忠  苟晓琴  刘四海  郑远川  张光辉 《高校地质学报》2007,13(2):207-223

白石头泉含黄玉的天河石花岗岩体Rb-Sr等时线年龄209.6±9.6 Ma，从下至上可分为5个连续过渡的岩相带，即淡色花岗岩（a带），含天河石花岗岩（b带），天河石花岗岩（c带），含黄玉天河石花岗岩（d带）以及黄玉钠长花岗岩（e带）。岩体的岩石地球化学特征是高F（> 2 %）、高 Rb (500×10-6～1 087×10-6)，低 P2O5 (≤0.06%)，Na2O>K2O，弱过铝 (A/NKC=1.00~1.11)、翼型稀土元素配分曲线 (ΣREE=28.6×10-6~231.9×10-6)、低(La/Lu)N值 (0.11~0.68)、强烈Eu负异常(Eu/Eu* = 0.0005~0.0110)、Nd同位素富集（εNd (t )= -4.4~-4.9）。该岩体的岩浆是中地壳云母片麻岩部分熔融的产物。从a带到e带的地球化学变化是：（1）F，A2O3和Na2O含量逐渐增加，而SiO2，（Fe2O3+FeO+MgO+MnO）、FeO和K2O含量逐渐减少，在标准矿物的Qz-Ab-Or图上总体向Ab角顶移动；（2）总体而言，Cr，Ni，Co，V，W，Nb，Zr，U，Th和Y含量逐渐减少，而F，Li，Rb，Hf，Ta，Sn，Sc，Ga和Zn含量逐渐增加，但d带到e带间存在Li，Rb，Sn，Sc和Zn含量的突降；（3）K/Rb，Al/Ga，Nb/Ta和Zr/Hf值下降， 但K/Cs，Th/U，(La/Lu)N值上升；（4）全岩的δ18O 值从a带的9.25 ‰~9.75 ‰降低到e带的7.32 ‰，d带与e带间存在2.1‰的δ18O值突降。岩浆从a带到e带的垂向分带是分离结晶和流体输运的共同结果。岩体的d带与e带存在明显的成分间断。在矿物成分上表现为黄玉、钠长石和白云母的剧增，钾长石和天河石的剧减。在主量元素上表现为 Na2O和CaO含量的剧增，SiO2和K2O含量的剧减。在微量元素上表现为F，Ga，Sr和Ba含量的剧增，Li，Rb，Sc，Zn和Sn含量的剧减。在稀土元素上，Eu/Eu*和(La/Lu)N值增加，而ΣREE值降低。在氧同位素特征上，δ18O值显著降低。这种间断不仅受分离结晶和流体输运的制约，也与天水加入、围岩混染和亚固相线淋滤有关。  相似文献   

安徽庐枞盆地中巴家滩岩体的岩石地球化学特征及成因   总被引：6，自引：5，他引：6  

刘珺　周涛发袁峰  范裕吴明安  陆三明钱存超 《岩石学报》2007,23(10):2615-2622

巴家滩岩体位于长江中下游庐枞中生代火山岩盆地的中心地带,出露面积约4km2.岩性主要为辉石二长岩和含英辉石二长岩,发育黄铁矿化和黄铜矿化.野外及室内证据表明该岩体可分为两期,第一期表现为闪长质岩石包体;第二期主要为旱阶段的辉石二长岩和晚阶段的含石英辉石二长岩.巴家滩岩体随着由早到晚的演化,其SiO2含量、总碱含量(Na2O K2O)和岩石的氧化度不断增高.稀土配分整体呈右倾趋势,轻稀土富集,重稀土分馏不明显.岩石学、稀土和微量元素地球化学特征表明巴家滩岩体成岩物质来源于富含金云母的富集地幔Ⅱ.巴家滩岩体属于橄榄玄粗岩系,形成于伸展构造环境.巴家滩岩体具有高Al2O2、Sr、St/Y、La/Yb,低Y、Yb、Sr正异常,Eu弱负异常,与沙溪岩体的特征相似,早期包体的Cu含量高达0.8402,推断在其深部可能有可能有类似沙溪岩体的矿化岩浆存在.  相似文献   

Development of a Continental Volcanic Field: Petrogenesis of Pre-caldera Intermediate and Silicic Rocks and Origin of the Bandelier Magmas, Jemez Mountains (New Mexico, USA)     

Rowe  M. C.; Wolff  J. A.; Gardner  J. N.; Ramos  F. C.; Teasdale  R.; Heikoop  C. E. 《Journal of Petrology》2007,48(11):2063-2091

The Miocene–Quaternary Jemez Mountains volcanic field(JMVF) is the site of the Valles caldera and associated BandelierTuff. Caldera formation was preceded by > 10 Myr of volcanismdominated by intermediate composition rocks (57–70% SiO₂)that contain components derived from the lithospheric mantleand Precambrian crust. Simple mixing between crust-dominatedsilicic melts and mantle-dominated mafic magmas, fractionalcrystallization, and assimilation accompanied by fractionalcrystallization are the principal mechanisms involved in theproduction of these intermediate lavas. A variety of isotopicallydistinct crustal sources were involved in magmatism between13 and 6 Ma, but only one type (or two very similar types) ofcrust between 6 and 2 Ma. This long history constitutes a recordof accommodation of mantle-derived magma in the crust by meltingof country rock. The post-2 Ma Bandelier Tuff and associatedrhyolites were, in contrast, generated by melting of hybridizedcrust in the form of buried, warm intrusive rocks associatedwith pre-6 Ma activity. Major shifts in the location, styleand geochemical character of magmatism in the JMVF occur withina few million years after volcanic maxima and may correspondto pooling of magma at a new location in the crust followingsolidification of earlier magma chambers that acted as trapsfor basaltic replenishment. KEY WORDS: crustal anatexis; fractional crystallization; Jemez Mountain Volcanic Field; Valles Caldera; radiogenic isotopes; trace elements  相似文献   

Analytical perspective on trace element species of interest in exploration   总被引：1，自引：0，他引：1  

Gwendy E. M. Hall 《Journal of Geochemical Exploration》1998,61(1-3)

Analysis of soil and sediment samples, using selective extraction methods to distinguish different phases, is of particular interest in exploration geochemistry to locate deeply buried mineral deposits. There are various mechanisms of binding labile elements in the secondary environment, including physical and chemical sorption, precipitation, chelation and complexation. Phases present in soils and sediments which are likely to scavenge ‘free' elements include amorphous Mn and Fe oxides, the humic and fulvic components of humus, and clays. This paper reviews these forms of trace elements and the methods in current use to quantify them. Examples of precision data, both for control and survey samples, are given with respect to trace elements dissolved from the ‘soluble organic' component of humus, Mn oxides and amorphous Fe oxides. The high sensitivity of inductively coupled plasma mass spectrometry (ICP–MS) is required to measure accurately and precisely a large suite of trace elements, especially where only small fractions of elements are dissolved by such leaches as the commercially available Enzyme and MMI (Mobile Metal Ion) extractions. The relative standard deviations (RSD) obtained for 33 elements (e.g. Ag, Cd, In, I) in the standard reference sample (SRM), TILL-2, are in the range 0.5–8% for the hydroxylamine hydrochloride (NH₂OH·HCl) leach designed to extract hydrous Fe and Mn oxides. The corresponding RSDs for elements in the reactive Mn oxide phase extracted by the Enzyme leach are in the range 3–19% except for some trace elements at levels close to detection limit (e.g. Cd, Bi). The RSDs obtained for field duplicates are inferior to those for analytical replicates (i.e. sample splits), probably a reflection of different concentrations of the host phase. In one soil survey, the Fe extracted by a 0.25 M NH₂OH·HCl leach ranged conservatively from 0.2 to 1.7% whereas the Mn extracted by the Enzyme leach varied extensively, from 0.3 to >999 ppm. In contrast, precision, at 1–7% RSD, for field duplicates was found to be comparable with that for both analytical duplicates and the SRM, LKSD-4, for elements associated with the humic and fulvic component of humus samples sieved to <177 μm.  相似文献   

岩浆侵位机制研究综述   总被引：10，自引：0，他引：10  

许顺山  吴淦国 《地质科技情报》1998,17(4):8-14

岩浆侵位机制是研究地球动力作用的重要依据,综合国内外资料,对岩浆侵位机制提出了按侵位深度,岩浆迁移距离,岩浆结晶程度的分类方案及其联合侵位类型。分别对各类侵位机制 岩浆侵位过程,特点,研究现状进行了综述,并讨论了岩浆定位空间问题和影响岩浆定位的因素。  相似文献   

Ca, Al-rich inclusions in Yamato 791717 (CO3) carbonaceous chondrite: Formation and alteration     

Yangting Lin  Daode Wang  Makoto Kimura 《中国科学D辑(英文版)》1998,41(5):513-521

In three polished thin sections of Yamato 791717 (CO3). fifty-five Ca, Al-rich inclusions were found, which include two hibonite-bearing, eight melilite-rich and forty-five spinel-pyroxene inclusions. Based on the petrography and mineral chemistry of the inclusions, it is proposed that the melilite-rich inclusions and spinel-pyroxene inclusions condensed in the solar nebula, and the hibonite-bearing inclusions crystallized from melts. The heavy alteration of the inclusions in Yamato 791717, which probably took place under a very oxidizing condition in the solar nebular, is also confirmed. Project supported by the National Natural Science Foundation of China (Grant No. 49673200). and by the Japanese Society for Promotion of Sciences (JSPS).  相似文献   

赛马-柏林川碱性杂岩常量组分变异的分离结晶制约     

谭东娟  林景仟  单玄龙 《吉林大学学报(地球科学版)》1998,(4)

赛马－柏林川碱性杂岩体为侵位于古元古宙与新元古宙之间的缓倾斜岩席状岩体,缓倾的张裂隙制约了分异岩浆的侵位和含矿溶液的流通,交代富集的上地幔产生的富碱岩浆与富集的地壳产生的岩浆以不同比例混合,形成了正长质岩浆和霞石正长质岩浆。含地壳组分较高的正长质岩浆,受富钙辉石、角闪石和镁质较高黑云母的结晶分离制约向硅酸过饱和方向演化;霞石正长质岩浆受富钙辉石—霓辉石、白榴石、含Ｆｅ较高黑云母、黑榴石的分离结晶制约发生分异。稀土元素矿床是霞石正长质岩浆分异残余熔体的产物,侵位于岩体最高层位。  相似文献   

Metal-residence sites in lavas and tuffs from Volcán Popocatépetl, Mexico: implications for metal mobility in the environment     

A. C. L. Larocque  James A. Stimac  Claus Siebe 《Environmental Geology》1998,33(2-3):197-208

 Volcan Popocatépetl is a Quaternary stratovolcano located 60 km southeast of Mexico City. The summit crater is the site of recent ash eruptions, excess degassing, and dacite dome growth. The modern cone comprises mainly pyroclastic flow deposits, airfall tephras, debris flows, and reworked deposits of andesitic composition; it is flanked by more mafic monogenetic vents. In least-degassed fallout tuffs and mafic scoria, transition metals are concentrated in phases formed before eruption, during eruption, and after eruption. Preeruptive minerals occur in both lavas and tephra, and include oxides and sulfides in glass and phenocrysts. The magmatic oxides consist of magnetite, ilmenite, and chromite; the sulfides consist of both (Fe,Ni)_1-xS (MSS) and Cu–Fe sulfide (ISS). Syn- and posteruptive phases occur in vesicles in both lavas and tephra, and on surfaces of ash and along fractures. The mineral assemblages in lavas include Cu–Fe sulfide and Fe–Ti oxide in vesicles, and Fe sulfide and Cu–Fe sulfide in segregation vesicles. Assemblages in vesicles in scoria include Fe–Ti oxide and rare Fe–Cu–Sn sulfide. Vesicle fillings of Fe–Ti oxide, Ni-rich chromite, Fe sulfide, Cu sulfide, and barite are common to two pumice samples. The most coarse-grained of the vesicle fillings are Cu–Fe sulfide and Cu sulfide, which are as large as 50 μ in diameter. The youngest Plinian pumice also contains Zn(Fe) sulfide, as well as rare Ag–Cu sulfide, Ag–Fe sulfide, Ag bromide, Ag chloride, and Au–Cu telluride. The assemblage is similar to those typically observed in high-sulfidation epithermal mineralization. The fine-grained nature and abundance of syn- and/or posteruptive phases in porous rocks makes metals susceptible to mobilization by percolating fluids. The abundance of metal compounds in vesicles indicates that volatile exsolution prior to and/or during eruption played an important role in releasing metals to the atmosphere. Received: March 1997 · Accepted: 27 May 1997  相似文献   

Phase Chemistry Study of the Zabuye Salt Lake Brine: Isothermal Evaporation at 15°C and 25°C     

NIE Zhen  BU Lingzhong  ZHENG Mianping  ZHANG Yongsheng 《《地质学报》英文版》2010,84(6):1533-1538

Zabuye Salt Lake in Tibet, China is a carbonate-type salt lake, which has some unique characteristics that make it different from other types of salt lakes. The lake is at the latter period in its evolution and contains liquid and solid resources. Its brine is rich in Li, B, K and other useful minor elements that are of great economic value. We studied the concentration behavior of these elements and the crystallization paths of salts during isothermal evaporation of brine at 15°C and 25°C. The crystallization sequence of the primary salts from the brine at 25°C is halite (NaCl) → aphthitalite (3K2SO4·Na2SO4) → zabuyelite (Li2CO3)→ trona (Na2CO3·NaHCO3·2H2O) → thermonatrite (Na2CO3·H2O) → sylvite (KCl), while the sequence is halite (NaCl) → sylvite (KCl) → trona (Na2CO3·NaHCO3·2H2O) → zabuyelite (Li2CO3) → thermonatrite (Na2CO3·H2O) → aphthitalite (3K2SO4·Na2SO4) at 15°C. They are in accordance with the metastable phase diagram of the Na+, K+-Cl?, CO32?, SO42?-H2O quinary system at 25°C, except for Na2CO3·7H2O which is replaced by trona and thermonatrite. In the 25°C experiment, zabuyelite (Li2CO3) was precipitated in the early stage because Li2CO3 is supersaturated in the brine at 25°C, in contrast with that at 15°C, it precipitated in the later stage. Potash was precipitated in the middle and late stages in both experiments, while boron was concentrated in the early and middle stages and precipitated in the late stage.  相似文献   

丁二酸桥联双核铜Cu(C_3N_2H_4)_2(C_4H_5O_4)_2晶体的超分子结构及形貌特征     

陈洪  胡波  吴秀玲  余小红  张荔  肖兵  于梅花  陈敬中 《矿物岩石》2010,30(1)

用XRD,SEM和TEM研究新型配合物Cu(C3N2H4)2(C4H5O4)2的超分子结构和微观形貌,并对新型晶体的平衡外形进行模拟计算,结果表明:该配合物分子具有丁二酸桥联的双核铜结构,中心铜离子处在2个咪唑和4个丁二酸以单齿配位组成的八面体中心,在ab平面,分子中有十四元大环,环内Cu(1)-Cu(2)原子间距为0.8031nm,C(2)-C(2′)为0.4183nm;在ac平面,沿着[010]方向分子内呈现凹的六边形纳米级孔洞;沿[100]方向分子依靠弱的氢键作用,层状堆积成三维超分子结构。此外,随着丁二酸的碳链沿[001]方向无限延伸,形成以铜离子为交叉中心的带状拓扑构型。SEM观察到晶体表面形成有明显的凹坑,区域呈现层状阶梯,说明晶体在(100)面遵照台阶-扭折模型呈层状生长结晶。TEM微区形貌像显示晶体存在条纹和缺陷结构,整体保持柱状构型,这与模拟的晶体平衡外形呈柱状一致。模拟结果表明晶体最易外显晶面为(100)面,外显比例达41.247%,这与晶体超分子层沿[100]方向通过氢键作用堆积,键作用力较弱密切相关。  相似文献