Geochemical Characteristics,Origin, and Evolution of Ore‐Forming Fluids of the Khut Copper Skarn Deposit,West of Yazd in Central Iran

The Khut copper skarn deposit is located at about 50 km northwest of Taft City in Yazd province in the middle part of the Urumieh‐Dokhtar magmatic arc. Intrusion of granitoid of Oligocene–Miocene age into carbonate rocks of the Triassic Nayband Formation led to the formation of marble and a calcic skarn. The marble contains high grade Cu mineralization that occurs mainly as open space filling and replacement. Cu‐rich sulfide samples from the mineralized marble are also anomalous in Au, Zn, and Pb. In contrast, the calcic skarn is only weakly anomalous in Cu and W. The calcic skarn is divided into garnet skarn and garnet–pyroxene skarn zones. Paragenetic relationships and microthermometric data from fluid inclusions in garnet and calcite indicate that the compositional evolution of skarn minerals occurred in three main stages as follows. (i) The early prograde stage, which is characterized by Mg‐rich hedenbergite (Hd_53.7Di_42.3–Hd_86.1Di_9.5) with Al‐bearing andradite (69.8–99.5 mol% andradite). The temperature in the early prograde skarn varies from 400 to 500°C at 500 bar. (ii) The late prograde stage is manifested by almost pure andradite (96.2–98.4 mol% andradite). Based on the fluid inclusion data from garnet, fluid temperature and salinity in this stage is estimated to vary from 267 to 361°C and from 10.1 to 21.1 wt% NaCl equivalent, respectively. Pyrrhotite precipitation started during this stage. (iii) The retrograde stage occurs in an exoskarn, which consists of an assemblage of ferro‐actinolite, quartz, calcite, epidote, chlorite, sphalerite, pyrite, and chalcopyrite that partially replaces earlier mineral assemblages under hydrostatic conditions during fracturing of the early skarn. Fluids in calcite yielded lower temperatures (T < 260°C) and fluid salinity declined to ～8 wt% NaCl equivalent. The last stage mineralization in the deposit is supergene weathering/alteration represented by the formation of iron hydroxide, Cu‐carbonate, clay minerals, and calcite. Sulfur isotope data of chalcopyrite (δ³⁴S of +1.4 to +5.2‰) show an igneous sulfur source. Mineralogy and mineral compositions of the prograde assemblage of the Khut skarn are consistent with deposition under intermediately oxidized and slightly lower fS₂ conditions at shallow crustal levels compared with those of other typical Fe‐bearing Cu–Au skarn systems.     

北秦岭板山坪岩体锆石U-Pb年代学及岩石成因研究

板山坪岩体是北秦岭二郎坪群中的侵入岩。为了查明该岩体的成因,对该岩体进行了锆石U-Pb年代学、锆石原位Hf同位素研究以及矿物化学分析等方面的研究。研究结果表明,板山坪岩体岩性组成主要为石英闪长岩和花岗闪长岩,花岗闪长岩内部存在暗色包体。本次研究获得板山坪石英闪长岩锆石U-Pb年龄为442.7～432.2 Ma,花岗闪长岩锆石U-Pb年龄为436.8～432.7 Ma,暗色包体锆石U-Pb年龄为437.6 Ma。锆石176Hf/177Hf值为0.282 737～0.282 736,εHf（t）值集中分布在8.4～9.4之间,二阶段Hf模式年龄（TDM2）在876～832 Ma之间。石英闪长岩结晶温压分别为673 ℃～745 ℃和0.19～0.54 GPa,花岗闪长岩结晶温压分别为657 ℃～730 ℃和0.48～0.96 GPa,暗色包体结晶温压分别为680 ℃～734 ℃和0.69～1.65 GPa。综合分析认为板山坪岩体为复式岩体,两期结晶年龄分别为496～487 Ma和442～432 Ma。岩石来源于地幔分离出来的新生下地壳。     

河南桐柏围山城地区主要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。     

Spatial variability of watermass conditions within the European Epicontinental Seaway during the Early Jurassic (Pliensbachian–Toarcian)

In order to constrain spatial variability in watermass conditions within the European Epicontinental Seaway prior to, during and after the Toarcian Oceanic Anoxic Event, carbon (δ¹³C_bel, δ¹³C_carb) and oxygen (δ¹⁸O_bel, δ¹⁸O_carb) isotope records were obtained from three sections in the Grands Causses Basin (southern France). These data were then compared with similar records along a north–south transect across the European Epicontinental Seaway. As the conclusions reached here strongly depend on the reliability of belemnite calcites as archives of palaeoceanographic changes, an attempt was made to improve the understanding of isotope signals recorded in belemnite calcite. Intra‐rostral carbon and oxygen‐isotope data from six belemnite specimens belonging to the genus Passaloteuthis were collected. Intra‐rostral carbon‐isotopes are influenced by vital effects, whereas oxygen‐isotopes reflect relative changes in temperature and salinity. Palaeotemperatures calculated from δ¹⁸O_bel‐isotope records from the Grands Causses Basin confirm relatively low temperatures throughout the Late Pliensbachian. Similar cool water conditions have previously been shown in Germany, England, Spain and Portugal. A temperature increase of up to 6 °C is observed across the Pliensbachian–Toarcian boundary. A pronounced negative shift of at least ?3‰ (Vienna‐Pee Dee Belemnite) is recorded in bulk carbonate carbon during the lower Harpoceras serpentinum zone, typical of the Toarcian Oceanic Anoxic Event. Before and after the Toarcian Oceanic Anoxic Event, a good correlation between δ¹³C_carb and δ¹³C_bel exists, indicating well‐ventilated bottom‐waters and normal marine conditions. Instead, data for the Toarcian Oceanic Anoxic Event indicate the development of a strong north–south gradient in salinity stratification and surface‐water productivity for the Western Tethyan realm. This study thus lends further support to a pronounced regional overprint on carbon and oxygen‐isotope records in epicontinental seaways.     

广西梧州思委银矿区花岗岩的岩石成因：锆石U-Pb测年、岩石地球化学和Hf同位素约束

本文对广西梧州思委银矿区思委岩体中细粒黑云母二长花岗岩进行了系统的锆石U-Pb年代学、岩石地球化学和Hf同位素分析研究,以深入探讨其岩石成因。LA-ICP-MS锆石U-Pb定年获得了思委岩体黑云母二长花岗岩成岩年龄为165±1Ma。思委岩体黑云母二长花岗岩为一套弱过铝质高钾钙碱性系列花岗岩,富集U、K、Pb等元素,亏损Nb、Ta、P、Ti等元素;球粒陨石标准化REE配分模式为右倾斜配分模式,轻重稀土元素分异强烈,富集轻稀土元素,重稀土元素平坦分布。锆石Hf同位素分析花岗岩锆石ε_(Hf)(t)值分布在-15.9~8.7之间,Hf同位素二阶段模式年龄(t2DM)在652~2255Ma之间,表明岩浆源区既有直接源于亏损地幔分异的新生地壳的迅速重熔,也有不同比例的古老地壳的混合作用。花岗岩成岩可能是受古太平洋板块持续俯冲作用影响,焊接板片开裂形成的岩浆上侵。     

白云鄂博赋矿白云岩与微晶丘和碳酸岩墙的碳氧同位素对比研究

本文通过方解石和白云石的碳和氧同位素分析,对比研究了白云鄂博赋矿白云岩、黑脑包微晶丘、北京西山微晶丘、宽沟北正常沉积灰岩和白云鄂博碳酸岩墙,从而探讨了赋矿白云岩的成因及其与超大型Fe-Nb-REE矿床的成因关系。结果为:①黑脑包腮林忽洞群顶部微晶丘和北京西山寒武系顶部微晶丘碳酸盐的δ~(13)C值都在0±2‰左右,δ~(18)O值为18.3‰～25.1‰,均具有典型海相沉积碳酸盐岩的特点;②白云鄂博东矿采场δ~(13)C值为-7.9‰～-1.1‰,δ~(18)O值为9.1‰～20.9‰;矿区东西两端δ~(13)C值-7.9‰～-0.6‰,δ~(18)O值8.6‰～25.7‰;均介于地幔流体与典型沉积碳酸盐岩之间。部分赋矿白云岩样品中白云石与方解石之间的碳氧同位素分馏△~(13)C和△~(18)O值均小于0‰,表明其受到过次生蚀变作用,低δ~(18)O值白云石样品所对应的负△~(18)O值反映了地幔镁质流体对沉积碳酸盐岩的强烈交代作用;③矿区—富稀土碳酸岩墙的δ~(13)C值为-7.2‰～-4.7‰,δ~(18)O价值为11.9‰～16.4‰,表明其碳酸岩岩浆并非原始地幔来源,而可能与俯冲板块携带的沉积碳酸盐岩与地幔流体在深部的高温混合熔融有关。碳酸岩墙中白云石与方解石之间的碳和氧同位素分馏均小于0‰,说明该碳酸岩墙中的白云石与方解石并非同成因矿物,至少其中之一为     

错流超滤技术在海水胶体态铀、钍、镭同位素和有机碳研究中的应用

建立了由预过滤装置、蠕动泵、中空纤维超滤膜(AmiconH10P10-20,标称截留分子量10KDa)和连接管组成的错流超滤系统,利用荧光标记的40KDa葡聚糖和已知放射性活度的234Th示踪剂评估了超滤膜的截留和吸附性质,探讨了234Th在超滤过程中的渗透行为,考查了该系统用于实际海水样品时铀、钍、镭同位素和有机碳的质量平衡状况.结果表明,10Kda中空纤维超滤膜对40Kda葡聚糖具有良好的截留效率(85%),而吸附损失率为18%.铀、钍、镭同位素和有机碳在超滤过程中均达到极佳的质量平衡,回收率R=95%～98%,优于大多数文献报道的值.234Th在超滤过程中的渗透行为可以很好地用渗透模型加以描述.研究组分胶体态含量占“溶解”态含量的份额大小顺序如下:钍同位素、有机碳、镭同位素约等于铀同位素,这与钍为强颗粒活性元素、铀和镭为水溶性元素的地球化学性质相吻合.     

长江流域河水和悬浮物的锂同位素地球化学研究

深入理解流域侵蚀过程中的锂同位素分馏对于运用锂同位素来示踪化学循环和气候变化是十分必要的。研究集中在长江干流和主要支流的水体和悬浮物的锂及锂同位素组成。长江流域水体的锂及锂同位素组成（δ⁷Li）分别为150~4 570 nmol/L和+7.6‰~+28.1‰,两者沿上游至下游的变化趋势相反。悬浮物锂同位素组成（δ⁷Li）变化比较稳定,分别为41~92 μg/g和-4.7‰~+0.7‰,而且总是低于相应水体的锂同位素组成。悬浮物和流体之间的锂同位素分馏系数在0.977和0.992之间,与悬浮物的量及组成存在明显相关性,反映了粘土矿物的吸附和化学风化的程度。锂含量与锂同位素组成之间良好的负相关性表明流域水体的锂来自2个端元混合：其一可能是蒸发盐岩,并伴有深部热泉水;其二可能是硅酸岩。     

U-Pb-Hf isotopic data from detrital zircons in late Carboniferous and Mid-Late Triassic sandstones,and also Carboniferous granites from the Tauride and Anatolide continental units in S Turkey: implications for Tethyan palaeogeography

ABSTRACT

Zircons from Carboniferous sandstones (three samples) and Mid-Late Triassic sandstones (four samples) from the Tauride and Anatolide continental units were analysed for U-Pb-Hf isotopes. For comparison, zircons were also analysed from Carboniferous granites of the Afyon Zone, Anatolides (three samples). A NE African/Arabian source is inferred for both the Carboniferous sandstones of the Taurides (Alada?) and the Anatolides (Konya Complex). In contrast, the Carboniferous Karaburun Melange is characterised by a NW African provenance. A prominent Devonian population occurs in the Carboniferous Karaburun Melange, characterised by mainly positive ε_Hf(t) values that differ significantly from those of the Devonian granites of the Sakarya continental crustal unit (Pontides). Middle-Late Triassic Tauride sandstones include minor Palaeozoic and Early Mesozoic zircons. In contrast, Devonian and Carboniferous zircons are relatively abundant in Late Triassic sandstones of the Karaburun Peninsula. The Hf isotopic compositions of 25 Carboniferous-aged zircons from three samples of Mid-Late Triassic sandstone and one of Late Carboniferous age (one sample) overlap with the ε_Hf(t) values of Carboniferous arc-type granites in the Anatolides. Taking account of the available U-Pb and Lu-Hf isotopic data from comparative crustal units, the Devonian zircon populations from the melanges in the Karaburun Peninsula and the Konya Complex are inferred to have a westerly source (e.g. granitic rocks of Aegean region or central Europe). A tectonic model is proposed in which Palaeozoic Tethys sutured during the late Carboniferous in the west (Aegean region westwards), leaving an eastward-widening oceanic gulf in which sandstone turbidites accumulated, including Devonian zircons.     

Use of an optical oxygen sensor to measure dissolved oxygen in seawater

The use of an optical oxygen sensor to measure dissolved oxygen in seawater was investigated. The sensor is based on the dynamic quenching of an oxygen-sensitive fluorochrome embedded in the tip. Dissolved oxygen in seawater samples collected from eight stations at depths ranging from 3000 to 6000 m was analyzed both with the optical sensor and by the Winkler titration method. The two sets of data did not differ significantly. The stability and simplicity of the method and the good agreement of the results with those of the titration method indicate that the sensor would be useful for fieldwork.