河南桐柏围山城地区侵入岩年代学与地球化学特征

河南省桐柏围山城地区位于华北板块与扬子板块之间的秦岭造山带与大别造山带的衔接部位,本文对产于该区的主要侵入岩体开展了锆石SHRIMP测年和岩石地球化学特征研究.总共对8件样品开展了SHRIMP测年,其中产于破山银矿区的云斜煌岩获得的锆石SHRIMP测年结果为461.8 ± 9.7 Ma,MSWD＝1.10,表明其形成于加里东中期.在桃园岩体及其南部混染带内产出的变辉长岩、石英闪长岩、花岗闪长岩和黑云母花岗岩共获得了6组年龄数据,分别是431.7 ± 8.3 Ma (MSWD＝0.76)、432.3 ± 7.5Ma (MSWD＝0.45)、470.3 ± 8.3Ma(MSWD＝1.3)、431.5 ± 8.2 Ma(MSWD＝1.6)、433 ± 11 Ma(MSWD＝1.8)和426.7 ± 9.1 Ma(MSWD＝1.6),说明桃园岩体是加里东晚期岩浆侵位产物.梁湾岩体花岗闪长岩和二长花岗岩的锆石SHRIMP测年结果分别为132.5 ± 2.3Ma (MSWD＝1.5)和137.0 ± 3.4Ma (MSWD＝1.9),为燕山中期.锆石SHRIMP测年结果表明,围山城地区主要侵入岩的岩浆活动集中在三个时期,分别是460～470Ma,430Ma和135Ma.侵入岩体的岩石地球化学研究结果表明,与加里东晚期花岗岩相比,燕山中期花岗岩明显富K、Nb和Rb贫Na和Y.Pb-Sr-Nd同位素示踪研究表明,加里东晚期花岗岩明显富含放射性成因Pb,其206Pb/204Pb值为19.342～19.712,平均值19.512,(87Sr/86Sr)i值较低,变化于0.70211~0.704899,εNd (t)值均为正值,变化范围为+3.55～+7.53,显示成岩物质来源较深,可能来自亏损地幔;而燕山中期花岗岩的放射性成因Pb含量低,206Pb/204Pb值为17.278～17.492,平均值17.370, (87Sr/86Sr)i值相对较高,为0.707004~0.716968,εNd(t)值均为较大负值,变化范围为-16.95～-9.76,显示成岩物质来源较浅,可能来自下地壳.围山城地区加里东晚期花岗岩与燕山中期花岗岩岩石地球化学特征上的差别与它们形成时所处的大地构造环境有关,加里东晚期花岗岩形成于弧后环境,而燕山中期花岗岩则形成于华北与扬子两大板块碰撞后的岩石圈减薄与伸展构造环境.     

新疆罗布泊盐湖氢氧锶硫同位素地球化学及钾矿成矿物质来源

罗布泊罗北凹地第四系上部盐层中蕴藏丰富的卤水,卤水中则富含钾（ＫＣｌ平均品位为１．４０％）。文章通过对罗布泊卤水氢、氧、锶及硫同位素等分析及与塔里木盆地（河流）、柴达木盆地等地区对比研究,确定了罗布泊富钾卤水源于地表水,可能主要是塔里木盆地南北缘河流水;卤水中的硫钾等物质组分主要来源于南天山、塔里木盆地西北、西南部中新生代石膏钙芒硝石盐矿床或地层及其古代地层卤水。由于第四纪期间塔里木盆地西部抬升。     

Carbon and Noble Gas Isotopes in the Tengchong Volcanic Geothermal Area, Yunnan, Southwestern China

Carbon and noble gas isotope analyses are reported for bubbling gas samples from the Tengchong volcanic geothermal area near the Indo-Eurasian suture zone. All samples contain a resolvable component of mantle-derived 3He. Occurrence of mantle-derived 3He coincides with surface volcanism. However, 3He occurs over a larger geographic areathan do surface volcanics. δ13C values for CO2 and CH4 vary from -33.4‰ to 1.6 ‰ and from -52.8‰ to -2.8‰, respectively. He and C isotope systematics indicate that CO2 and CH4 in the CO2-rich gases originated predominantly from magmatic component mixed with crustal CO2 produced from carbonate. However, breakdown of organic matter and near-surface processes accounts for the CH4 and CO2 in N2-rich gases. 3He/4He ratio distribution pattern suggests that mantle-derived He and heat sources of high-temperature system in central Tengchong originate from a hidden magma reservoir at subsurface. CO2-rich gases with the highest 3He/4He ratio (5.2 Ra) may be representative of the     

新疆阿尔泰巴特巴克布拉克铁矿床成矿作用研究

巴特巴克布拉克铁矿床赋存于上志留-下泥盆统康布铁堡组变质火山-沉积岩系中, 近矿围岩为石榴子石矽卡岩、角闪斜长变粒岩和浅粒岩。矿体总体顺层分布, 呈似层状、透镜状及不规则状, 空间上与矽卡岩密切相关。流体包裹体研究表明, 矽卡岩阶段形成的石榴子石中发育纯气体包裹体、气体包裹体、液体包裹体、含子矿物包裹体及熔融包裹体; 退化蚀变阶段发育液体包裹体和少量气体包裹体; 石英-硫化物阶段主要发育液体包裹体、含液体CO₂的三相包裹体及少量纯气体包裹体、气体包裹体和含子矿物包裹体。矽卡岩阶段均一温度变化为217 ℃~499 ℃, 在255 ℃出现峰值, 盐度(NaCl_eq)变化为8.68%~22.65%; 退化蚀变阶段均一温度变化为181 ℃~432 ℃, 在225 ℃出现峰值, 盐度变化为12.85%~22.65%; 石英-硫化物阶段均一温度变化为140 ℃~482 ℃, 在155 ℃出现峰值, 盐度变化为0.18%~42.40%。石榴子石、石英和方解石的 δ¹⁸ O_SMOW 变化为1.8‰~7.1‰, δ¹⁸Ο_Η2Ο为 -4.79‰~4.57‰, δD_SMOW 为 -128‰~-84‰, 表明矽卡岩阶段成矿流体主要为岩浆水, 混合少量大气降水; 石英-硫化物阶段大气降水所占比例明显增加。方解石δ¹³ C_V-PDB 变化为 -3.2‰~-2.0‰, 表明流体中的碳来自深部或地幔。     

安徽黄梅尖地区基性岩脉K-Ar年代学、地球化学特征及地质意义

在野外地质调查和室内综合研究的基础上,通过对黄梅尖地区辉绿玢岩K-Ar年代学、地球化学和Sr-Nd同位素特征进行研究,探讨辉绿玢岩的形成时代、岩石成因及构造背景。K-Ar年代学研究表明,辉绿玢岩形成于~107 Ma,是早白垩世岩浆活动的产物,形成时代晚于该地区火山岩和侵入岩,与该地区铀成矿年龄基本一致;辉绿玢岩的侵入可能是该地区岩浆作用的最后一幕,铀成矿可能与辉绿玢岩具有成因联系。地球化学特征表明,辉绿玢岩富集大离子亲石元素K、Rb、U、Pb和轻稀土元素,亏损高场强元素Nb、Ta、P、Ti,具有较高的Isr值和负εNd(t)值,具有富集地幔源区特征;辉绿玢岩是在地壳伸展和岩石圈减薄的构造背景下,由俯冲交代作用形成的富集地幔部分熔融形成的,表明~107 Ma时该地区仍处于伸展构造环境下。     

Lead isotope evolution of the Central European upper mantle:Constraints from the Bohemian Massif

The Pb isotope composition of the upper mantle beneath Central Europe is heterogeneous due to the subduction of regionally contrasting material during the Variscan and Alpine orogenies.Late Variscan to Cenozoic mantlederived melts allow mapping this heterogeneity on a regional scale for the last ca.340 Myr.Late Cretaceous and Cenozoic anorogenic magmatic rocks of the Bohemian Massif(lamprophyres,volcanic rocks of basanite/tephrite and trachyte/phonolite series) concentrate mostly in the Eger Rift.Cretaceous ultramafic lamprophyres yielded the most radiogenic Pb isotope signatures reflecting a maximum contribution from metasomatised lithospheric mantle,whereas Tertiary alkaline lamprophyres originated from mantle with less radiogenic ~(206)Pb/~(204)b ratios suggesting a more substantial modification of lithospheric source by interaction with asthenosphericderived melts.Cenozoic volcanic rocks of the basanite/tephrite and trachyte/phonolite series define a linear mixing trend between these components,indicating dilution of the initial lithospheric mantle signature by upwelling asthenosphere during rifting.The Pb isotope composition of Late Cretaceous and Cenozoic magmatic rocks of the Bohemian Massif follows the same Pb growth curve as Variscan orogenic lamprophyres and lamproites that formed during the collision between Laurussia,Gondwana,and associated terranes.This implies that the crustal Pb signature in the post-Variscan mantle is repeatedly sampled by younger anorogenic melts.Most Cenozoic mantle-derived rocks of Central Europe show similar Pb isotope ranges as the Bohemian Massif.     

High-frequency climatic oscillations during the last deglaciation as revealed by oxygen-isotope records of benthic organisms (Ammersee,southern Germany)

High-resolution oxygen-isotope records of benthic ostracods and molluscs from Ammersee, southern Germany, show high-frequency climatic changes during the last deglaciation and parallel in great detail published faunal and floral variations reconstructed from Norwegian Sea sediments and isotope variations in Greenland ice cores. The marine and the terrestrial records give evidence of a synchronous late glacial climatic development in Greenland, NW- and Mid-Europe. However,¹⁴C-ages of the supraregional climatic events and of two tephra layers in the marine sediments of the northeastern Atlantic Ocean are significantly older than the¹⁴C-ages of the corresponding horizons on land. These differences strongly suggest that major short-term events have affected the exchangeable carbon on earth during the dramatic environmental changes related to the deglaciation and in particular have affected the CO₂-distribution within the ocean and between ocean and atmosphere. Dating methods independent of climatic variations and of the global carbon budget should be given priority to refine the timescales of the marine and atmospheric processes during the last deglaciation.This is the fourth paper in a series of papers published in this issue on high-resolution paleolimnology. These papers were presented at the Sixth International Palaeolimnology Symposium held 19–21 April, 1993 at the Australian National University, Canberra, Australia. Dr. A. F. Lotter and Dr. M. Sturm served as guest editors for these papers.     

辽宁朝阳小塔子沟-东五家子金矿田地球化学特征

在朝阳小塔子沟-东五家子金矿田范围内,北地金矿、小塔子沟金矿和东五家子金矿,因距离岩体的远近不同,形成了不同的特征.石英流体包裹体研究表明,位于岩体内接触带的北地金矿为中温、中-深成热液矿床,位于岩体外接触带的小塔子沟金矿为中温、中成热液矿床,远离岩体的东五家子金矿为中-低温、浅成热液矿床.氢、氧同位素研究表明,北地金矿和小塔子沟金矿的成矿流体主要为岩浆水,东五家子金矿的成矿流体为岩浆水和大气降水混合成因.微量元素研究表明,北地金矿矿石以Mo、Bi等元素相对富集为特征,小塔子沟金矿矿石以Cu、Zn等元素相对富集为特征,东五家子金矿矿石以Pb、Ag等元素相对富集为特征.矿床离岩体越远,金矿物中Au/Ag比值越小.     

Anthropogenic nitrogen deposition induces rapid ecological changes in alpine lakes of the Colorado Front Range (USA)

Recent sediments from two alpine lakes (> 3300 m asl) in the Colorado Front Range (USA) register marked and near-synchronous changes that are believed to represent ecological responses to enhanced atmospheric deposition of fixed nitrogen from anthropogenic sources. Directional shifts in sediment proxies include greater representations of mesotrophic diatoms and increasingly depleted ¹⁵N values. These trends are particularly pronounced since ~ 1950, and appear to chronicle lake responses to excess N derived from agricultural and industrial sources to the east. The rate and magnitude of recent ecological changes far exceed the context of natural variability, as inferred from comparative analyses of a long core capturingthe entire 14,000-year postglacial history of one of the lakes. Nitrogen deposition to these seemingly pristine natural areas has resulted in subtle but detectable limnological changes that likely represent the beginning of a stronger response to nitrogen enrichment.     

三元体系CaCl2?SrCl2?H2O的相平衡及其在钙锶分离中的应用

采用等温溶解平衡法研究了三元体系CaCl₂?SrCl₂?H₂O温度从323.15 K到353.15 K范围内的相平衡。基于该三元体系多温下的相平衡数据,设计开展了实验室模拟南翼山油田卤水中氯化钙和氯化锶在温度323.15 K下的分离实验。实验室模拟钙锶分离实验结果表明,在323.15 K下时分离一次固相产品中的钙锶摩尔比可以从25.46:1降至1.73:1,SrCl₂的回收率为52.47 %,所得一次固相产品在323.15 K下溶解并再次蒸发。钙和锶的摩尔比从1.73:1降至1.1:1,SrCl₂的回收率为78.67 %。