西成铅锌矿化集中区热水沉积成矿作用的岩矿证据

热水沉积成矿与正常沉积矿床在矿质来源和成矿机制上有很大的差异 ,反映在岩矿石结构构造上也有明显的差异性。虽然都有特征的沉积韵律条带、纹层构造 ,但由于热水沉积成矿矿质浓度大而形成了稠密而富集的组构 ,二者可区分。通过对西成铅锌矿化集中区两类热水沉积矿床的岩矿石组构进行论证 ,认为他们不但以上述特征区别于正常沉积矿床 ,而且各自也有差异 ,厂坝式矿床在组构上保留了原始沉积富而大的特点 ,虽有矿物粒度在变质作用中重结晶加粗的富集过程 ,但没有完全破坏原始的热水沉积构造。毕家山式矿床也具有原始沉积特点 ,但在改造过程中有热液叠加交代充填的现象 ,而原始沉积特点则又可区别于热液矿床 ,硅质岩的结构构造就是明显的证据。     

新疆塔木铅锌矿成矿流体特征与矿床成因

新疆塔木铅锌矿赋存于石炭系碳酸盐岩断层破碎带中,矿体和手标本尺度呈现管/脉构造特点。管/脉壁主要由闪锌矿、方铅矿构成,管/脉中心充填白云石Ⅱ,管内可见钡-钾长石微粒,暗示成矿流体淋滤下伏地质体。充填期白云石Ⅱ较第Ⅰ期白云岩化灰岩表现出贫13C、18O的特点,反映成矿过程可能存在贫13C、18O的物质加入。鉴于白云石Ⅱ流体包裹体均一温度为119～191℃、闪锌矿流体包裹体存在CH4、C2H6、H2S气相组分、邻区达木斯乡和什拉甫剖面下石炭统有4个沥青显示点和24个荧光显示点、麦盖提斜坡海相石炭系曲1井、麦3井原油δ13C介于-34‰～-31‰之间及流体包裹体液相组分未见SO42-,可以推测成矿作用与热化学硫酸盐还原(TSR)过程相关。综合上述因素,可以认为新疆塔木铅锌矿为后生的与TSR作用相关的矿床。     

Fine-particle Mn and other metals linked to the introduction of MMT into gasoline in Sydney, Australia： Results of a natural experiment

PM2.5 particulates were analyzed using accelerator-based ion beam methods for a suite of 21 species （H, C, Na, Al, Si, P, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Br, Pb） to evaluate the contribution to Sydney air associated with the introduction of MMT as a replacement for Pb. MMT was discontinued in 2004. Teflon filters continuously sampled for 7 years from 1998 to 2004 were analyzed from two sites： a suburb （Mascot） close to the Central Business District [CBD （n=718）] and a high trafficked area, and a relatively rural （background） setting, ～20 km west of the CBD （n=730）. Mean Mn concentrations in air at the background site increased from 1.5- 1.6 ng/m^3 to 〈2 ng/m^3 at the time of the greatest MMT use whereas those at Mascot increased from about 2 to 5 ng/m^3. From the maximum values, the Mn showed a steady decrease at both sites concomitant with the decreasing use of MMT. Lead concentrations in air at both sites decreased from 1998 onwards, concomitant with the phase out of leaded gasoline in 2002. A high correlation was obtained for the relationship between Mn in air and lead replacement gasoline （LRG） use （R2 0.83） and an improved correlation for Mn/Al＋Si＋K and LRG use （R2 0.93）. With Mn concentrations normalized to background values of Al＋Si＋K to account for the lithogenically-derived Mn, the proportion of anthropogenic Mn was -70%. Changes for Mn and Pb in the particulates are attributed to the before-during-after use of MMT and decreasing use of Pb in gasoline.     

新疆阿舍勒火山岩型块状硫化物铜矿硫、铅同位素地球化学

通过对矿石矿物与容矿围岩Ｓ、Ｐｂ同位素地球化学的研究，证实阿舍勒铜矿区Ⅰ号矿床与Ⅱ号矿床在成因上具有显著差异，即Ⅰ号矿床成矿金属与细碧岩同源，硫则来自于火山喷气；Ⅱ号矿床成矿金属可能来自石英角斑质凝灰岩的海水淋滤，硫可能是多源的。这一认识为开拓找矿思路提供了新的依据。铅同位素资料还反映基－酸性火山岩来自两个源区。     

大沟谷钠长石岩型金矿床Pb、S、Sr同位素特征初探

大沟谷金矿床产于震旦系乐晶峡群钠长石岩带底部陡倾斜钠长石岩中。金矿床铅同位素组成变化大^206Pb/^204Pb17.356-19.306,^207Pb/^204Pb15.330-15.862,^208Pb/^204Pb37.532-39.957。u值在8.23-10.6之间，黄铁矿δ^34S值在5.1‰-13.4‰之间，铅同位素组成具线性相关关系，^206Pb/^204Pb与^207Pb/^204Pb线性方程y=0.24x 11.19,r=0.83,^206Pb/^204Pb与^208Pb/^204Pb方程为y=1.3x 14.8,r=0.93，黄铁矿铅硫同位素组成具负相关关系，钠长石岩Rb、Sr含量较低，^87Sr/^86Sr值为0.72263-0.73150，平均0.72595。综合铅、锶、硫同位素特征，可以认为大沟谷金矿床成矿物质主要来自高u值基底碎屑沉积岩及钠化基性火成岩。     

安徽省东至县查册桥金矿地质特征及硫铅同位素示踪

东至县查册桥金矿位于扬子陆块北缘,矿床规模达中型。为了解成矿物质来源,对查册桥金矿矿石进行了硫、铅同位素分析。结果显示:δ(34S)变化范围为1.8×10~(-3)～18.1×10~(-3),平均值为11.09×10~(-3),较集中分布在10×10~(-3)～15×10~(-3)之间,分布宽泛;矿石硫化物矿物206 Pb/204 Pb值介于17.954～19.748之间,207 Pb/204 Pb值介于15.608～15.786之间,208 Pb/204 Pb值介于38.107～39.411之间,它们的μ值9.43～9.77;ω值32.63～38.83;w(Th)/w(U)值介于3.31～3.93,Δβ值18.45～30.06;Δγ值22.96～57.97。硫、铅同位素特征表明查册桥金矿床成矿物质主要来源于上地壳,其形成与陆内造山作用和岩浆作用密切相关。     

Mineralogy and Isotope Geochemistry of Active Submarine Hydrothermal Field at Suiyo Seamount, Izu–Bonin Arc, West Pacific Ocean

This report presents mineralogical, geochemical and isotopic data on samples obtained using the Benthic Multi‐coring System (BMS) to drill a submarine hydrothermal deposit developed in a caldera on the summit of the Suiyo Seamount in the Izu–Bonin Island Arc, south of Japan. This deposit is regarded as the first example of Kuroko‐type sulfide mineralization on a volcano at the volcanic front of an island arc. The mineralization and hydrothermal alteration below the 300 × 150‐m area of active venting was investigated to depths of 2–9 m below the sea floor. Drilling beneath the area of active venting recovered a sequence of altered volcanic rocks (dacite lavas, pyroclastic rocks of dacite–rhyolite compositions and pumice) associated with sulfide veining and patches/veins of anhydrite. No massive sulfide was found, however, and the subsea‐floor mineralization to 10 m depth is dominated by anhydrite and clay minerals with some sulfides. Sulfide‐bearing samples contained high Au (up to 42 ppm), Ag (up to 263 ppm), As (up to 1550 ppm), Hg (up to 55 ppm), Sb (up to 772 ppm), and Se (up to 24 ppm). Electron probe microanalyzer indicated that realgar, orpiment, and mimetite were major As‐bearing minerals. The sulfides were also characterized by high Zn (>10%) compared to Cu (<6.3%) and Pb (<0.6%). The δ²⁰²Hg/¹⁹⁸Hg, δ²⁰²Hg/¹⁹⁹Hg and δ²⁰²Hg/²⁰⁰Hg of the sulfide‐bearing dacite samples and a sulfide chimney decreased with increasing Hg/Zn concentration ratio. The variation of the δ²⁰²Hg/¹⁹⁸Hg ranged from ?2.8 to +0.5‰ to relative to S‐HG02027. The large range of these δ²⁰²Hg/¹⁹⁸Hg was greater than might be expected for such a heavy element and may be due to a predominance of kinetic effects. The variation of δ²⁰²Hg/¹⁹⁸Hg of sulfide‐bearing dacite samples suggested that light Hg isotope in the vapor mixed with oxygenated seawater near sea floor during mineralization. Lead isotope ratios of the sulfide were very similar to those of the dacite lava, suggesting that lead is of magmatic origin. The ⁸⁷Sr/⁸⁶Sr ratio (0.70872) of anhydrite was different from that of the dacite lava, and suggests an Sr derivation predominantly from seawater. Hydrothermal alteration of the dacite in the Suiyo hydrothermal field was characterized by Fe‐sulfides, anhydrite, barite, montmorillonite, chlorite/montmorillonite mixed‐layer minerals, mica, and chlorite with little or no feldspar or cristobalite. Hydrothermal clay minerals changed with depth from montmorillonite to chlorite/montmorillonite mixed‐layer minerals to chlorite and mica. Hydrogen isotope ratios of chlorite/montmorillonite and mixed‐layer, mica‐chlorite composites obtained below the active venting sites ranged from ?49 to ?24‰, suggesting seawater as the dominant fluid causing alteration. Oxygen isotope ratios of anhydrite ranged from 9.2 to 10.4‰ and anhydrite formation temperatures were calculated to be 188–207°C. Oxygen isotope ratios ranged from +5.2 to +9.2‰ for montmorillonite, +3.2 to +4.5‰ for chlorite/montmorillonite mixed‐layer minerals, and +2.8 to +3.8‰ in mixtures of chlorite and mica. The formation temperatures of montmorillonite and of the chlorite–mica mixture were 160–250°C and 230–270°C, respectively. The isotope temperatures for clay minerals (220–270°C) and anhydrite (188°C) were significantly lower than the borehole temperature (308.3°C) measured just after the drilling, suggesting that temperature at this site is now higher than when clay minerals and anhydrite were formed.     

Use of Pb/Pb ratios to investigate the surface integrity of peat cores used to study the recent depositional history and geochemical behaviour of inorganic elements in peat bogs

The well characterised temporal trend in the ²⁰⁶Pb/²⁰⁷Pb atom ratio of atmospheric lead deposition in Scotland during the 20th century was used to investigate the surface integrity of several cores collected by different methods from Flanders Moss ombrotrophic peat bog, central Scotland, during 1996–2001. Based on ²⁰⁶Pb/²⁰⁷Pb profile comparisons, in conjunction with identified ²¹⁰Pb radionuclide inventory deficits for two of the cores, it was deduced that 25 ± 7 yrs worth of material was missing from the more seriously affected core. After allowing for an appropriate vertical offset based on ²⁰⁶Pb/²⁰⁷Pb profile matching, the subsequent matching of profiles of titanium, lead, sulfur, arsenic, iron, phosphorus and manganese in three cores for which total concentration data were available was excellent. Without such offset correction, erroneous conclusions could have been drawn concerning the recent historical record of anthropogenic lead and arsenic deposition, the position of the redox boundary, which controls geochemical cycling and enrichment of iron, and the nutrient recycling status of manganese and phosphorus in the near-surface vegetation. Topographic, vegetative and coring (both device and operator) influences may have been responsible, thus endorsing the use of reliable, multiple core sampling and the use of lead isotope ratio profiles, supplemented by appropriate radionuclide data, in both assessing and ensuring the surface integrity of peat cores.     

内蒙古小西沟铅锌矿床矿石特征及可选性试验研究

小西沟锌铅矿床属于低温热液型矿床,矿石组成复杂,伴生铜和银,研究表明,该矿床矿石中的铅、锌、铜和银主要矿化元素以独立矿物产出,但部分黄铜矿与闪锌矿呈固溶体交生。根据矿石性质确定,该矿床矿石可采用混合浮选铜铅(铜、铅分离)—再浮选锌的工艺流程,通过试验获得符合标准的铜精矿、铅精矿和锌精矿,所用药剂没有环境污染,符合当前技术条件,可以开发利用。     

山东五莲七宝山地区长老庄隐爆角砾岩带特征及意义

七宝山金铜矿位于胶莱盆地西南缘的七宝山地区,在金铜矿外围新发现长老庄含矿隐爆角砾岩带一条, 物探解译工作初步查明了该隐爆角砾岩带地质及地球物理特征：位于激电中梯高阻和低阻接触带上,深部呈低阻、中高激化异常。经钻探验证,在深部发现高品位的银铜铅矿体,矿石中粗粒方铅矿、黄铜矿结晶体肉眼可见,呈团块状富集,铜品位0.493%～5.125%,铅品位0.245%～6.606%,银品位55.2～547.1g/t。表明在金铜矿外围及深部仍具有寻找隐爆角砾岩型高品位银铜铅矿体的潜力。