Genesis of the Huangshannan high-Ni tenor magmatic sulfide deposit in the Eastern Tianshan,northwest China: Constraints from PGE geochemistry and Os–S isotopes

The Huangshannan magmatic Ni-Cu sulfide deposit is one of a group of Permian magmatic Ni-Cu deposits located in the southern Central Asian Orogenic belt in the Eastern Tianshan, northwest China. It is characterized by elevated Ni tenor (concentrations in recalculated 100% sulfide) in sulfide within ultramafic rocks (9–19 wt%), with values much higher than other deposits in the region. Sulfides of the Huangshannan deposit are composed of pentlandite, chalcopyrite, and pyrrhotite and the host rock is relatively fresh, indicating that the high-Ni tenor is a primary magmatic feature rather than formed by alteration processes. It is shown that sulfides with high-Ni tenor can be generated by sulfide-olivine equilibrium at an oxygen fugacity of QFM +0.5, for magmas containing 450 ppm Ni and 20% olivine. Ores with >10 wt% sulfur have relatively low PGE and Ni tenors compared to other ores, R factor (mass ratio of silicate to sulfide liquid) modeling of Ni indicates that they formed at moderate R values (150–600). Based on this constraint on R values, ores with <10 wt% sulfides in the Huangshannan deposit can be segregated from a similar parental magma with 0.05 ppb Os, 0.023 ppb Ir, and 0.5 ppb Pd at R values between 600 and 3000. This, coupled with the supra-cotectic proportions of sulfide liquid to cumulus silicates in the Huangshannan ores imply mechanical transport and deposition of sulfide liquid in a magma pathway or conduit, in which sulfides must have interacted with large volumes of silicate magma. Platinum and Pd depletion relative to other platinum group elements (PGEs) are observed in fresh and sulfide-rich samples (S > 4.5 wt%). As sulfide-rich samples are also depleted in Cu, and as interstitial sulfides in those samples are physically interconnected at a scale of several cms, the low Pt and Pd anomalies are attributed to solid Pt and Pd phases crystallization and retention with the monosulfide solid solution (MSS) and Cu-rich sulfide liquid percolation during MSS fractionation. This finding indicates that Pt anomalies in sulfide-rich rocks from magmatic Ni-Cu deposits in the Eastern Tianshan are the result of sulfide fractionation rather than a hydrothermal effect. ¹⁸⁷Os/¹⁸⁸Os_(278Ma) values of the lherzolite samples vary from 0.27 to 0.37 and γOs_(278Ma) values vary from 110 to 189, indicating significant magma interaction with crustal sulfides, rich in radiogenic Os. Well constrained γOs values and δ³⁴S values (−0.4 to 0.8‰) indicate that crustal contamination occurred at depth before the arrival of the magma in the Huangshannan chamber. Regionally, deposits with high-Ni tenor have not been reported other than the Huangshannan deposit; however, many intrusions with high-Ni contents in olivine are present in NW China, such as the Erhongwa, Poyi and Poshi intrusions. Those intrusions are capable of forming high-Ni tenor sulfides due to olivine-sulfide-silicate equilibrium and relative high-Ni content in parent magma, making them attractive exploration targets.     

东昆仑夏日哈木镍铜硫化物矿床成矿岩浆条件:流体挥发份化学组成与碳同位素组成制约

夏日哈木镍铜硫化物矿床是我国东昆仑造山带新发现的全球岛弧环境最大的岩浆镍铜硫化物矿床。早泥盆世镁铁-超镁铁质成矿岩体中不同类型岩石的辉石中流体挥发份化学组成和碳同位素组成表明,流体挥发份总量较低,平均含量为888mm~3.STP/g(STP:标准温度和大气压)。流体挥发份组成以H_2O为主(48mol%),其次为H_2(26%)、CO_2(15%)和CO(5%)。H_2S含量从二辉橄榄岩(10mm~3/g)、橄榄辉石岩(18mm~3/g)到二辉辉石岩(28mm~3/g)逐渐增加,表明岩浆就位结晶演化过程中含硫组分的加入。CO_2的δ~(13)C值(-23.5‰~-5.0‰)位于地壳和地幔值范围之间。CH_4同系物碳同位素组成随碳数具有总体正序、局部反序的分布特征,显示大洋沉积有机质热裂解成因特征。夏日哈木成矿镁铁-超镁铁质岩体流体组分中较低的H2_O含量和较高的H_2含量表明,岩浆演化处于还原性挥发份条件,地幔岩浆源区存在俯冲洋壳沉积有机质,岩浆房围岩的混染和富S流体的加入可能是夏日哈木岩浆镍铜硫化物矿床硫饱和的主要机制。     

黄河北煤田岩浆岩侵入区内矿井地温分布规律研究—以潘店井田为例

通常情况下,地温会随深度增加而呈线性增加,地温影响着井下采掘工作面的环境温度。随着矿井深度的变化,空气所受到的压力状态也随之发生改变。当风流沿井巷向下流动时,空气的压力值增大。空气的压缩会出现放热(或吸热),从而使矿井温度升高。随着矿井向深部开采,井下作业环境条件恶化,岩层温度将达到摄氏几十度的高温。新汶孙村煤矿-800 m水平部分工作面温度高达30~33℃,巨野矿区龙固矿井-850 m水平所有工作面温度高达34~36℃,已严重影响了工人劳动效率。黄河北煤田潘店井田东部有燕山期岩浆岩活动,含煤地层的上中下部均有岩浆岩侵入,针对岩浆岩侵蚀地区采用钻孔简易测温和近似稳态测温等手段,详细查明地温分布规律,通过区内地温资料对比发现,该区有岩浆岩侵蚀影响的地段比没有岩浆岩侵蚀的地段地温高2.6~7.2℃。     

基于地震作用和场地影响确定广东省设计地震动参数

在对《建筑抗震设计规范(GB50011-2001)》和《建筑工程抗震性态设计通则(试用,CECS 160:2004)》研究的基础上,根据广东地区的场地和地震作用特点,确定出了广东省甲、乙、丙类建筑不同设防水准的地震动峰值加速度,以及广东省91个城镇的特征周期分区值,为广东省建筑物抗震设计提供了更加可靠的地震动参数。     

粉质黏土强度指标的水化学敏感性研究

通过对重塑粉质黏土的液、塑限和固结慢速直剪试验,探讨了粉质黏土液限、塑性指数及抗剪强度与不同浓度NaCl孔隙溶液的关系。试验结果表明,随着孔隙溶液浓度增加,液限随之减小,塑性指数表现出粉土的性质;不同竖向正应力下的强度随浓度变化表现出较大的差异,正应力较低时,强度不断减小,而正应力较高时,则强度不断增大,正应力介于二者之间强度则先降后升;内摩擦角随浓度增加而增大,最终趋于稳定;黏聚力先迅速减小后逐渐回升,且均为负值。其性质变化主要是因为扩散双电层、颗粒间作用力以及孔隙比发生了改变。基于Terzaghi的有效应力原理,对饱和粉质黏土固结慢速直剪试验测得的负值黏聚力进行了分析和讨论,认为渗透压力对黏聚力起了非常重要的作用,从而使黏聚力成为负值。     

近场地震作用下不规则层间隔震结构的动力响应分析

层间隔震结构作为一种新型的隔震形式,不仅可以降低上部结构的动力响应,还可以弥补基础隔震结构的不足.现有研究多集中在远场地震作用下的规则层间隔震结构.本文利用通用结构分析与设计软件SAP2000分别模拟了一幢8层带裙房钢筋混凝土框架层间隔震结构、基础隔震结构和抗震结构,分析并对比了三种结构在近场地震作用下动力响应特征.结果表明在近场条件下三种结构顶层均出现不同程度的鞭梢效应;相比抗震结构两种隔震结构具有很好的减震效果,而且基础隔震结构的减震效果好于层间隔震结构;由于结构刚度突变的部位剪力较大,所以应对其裙楼顶部予以加强.     

Evaluating legacy contaminants and emerging chemicals in marine environments using adverse outcome pathways and biological effects-directed analysis

Natural and synthetic chemicals are essential to our daily lives, food supplies, health care, industries and safe sanitation. At the same time protecting marine ecosystems and seafood resources from the adverse effects of chemical contaminants remains an important issue. Since the 1970s, monitoring of persistent, bioaccumulative and toxic (PBT) chemicals using analytical chemistry has provided important spatial and temporal trend data in three important contexts; relating to human health protection from seafood contamination, addressing threats to marine top predators and finally providing essential evidence to better protect the biodiversity of commercial and non-commercial marine species. A number of regional conventions have led to controls on certain PBT chemicals over several years (termed ‘legacy contaminants’; e.g. cadmium, lindane, polycyclic aromatic hydrocarbons [PAHs] and polychlorinated biphenyls [PCBs]). Analytical chemistry plays a key role in evaluating to what extent such regulatory steps have been effective in leading to reduced emissions of these legacy contaminants into marine environments. In parallel, the application of biomarkers (e.g. DNA adducts, CYP1A-EROD, vitellogenin) and bioassays integrated with analytical chemistry has strengthened the evidence base to support an ecosystem approach to manage marine pollution problems. In recent years, however, the increased sensitivity of analytical chemistry, toxicity alerts and wider environmental awareness has led to a focus on emerging chemical contaminants (defined as chemicals that have been detected in the environment, but which are currently not included in regulatory monitoring programmes and whose fate and biological impacts are poorly understood). It is also known that natural chemicals (e.g. algal biotoxins) may also pose a threat to marine species and seafood quality. Hence complex mixtures of legacy contaminants, emerging chemicals and natural biotoxins in marine ecosystems represent important scientific, economic and health challenges. In order to meet these challenges and pursue cost-effective scientific approaches that can provide evidence necessary to support policy needs (e.g. the European Marine Strategy Framework Directive), it is widely recognised that there is a need to (i) provide marine exposure assessments for priority contaminants using a range of validated models, passive samplers and biomarkers; (ii) integrate chemical monitoring data with biological effects data across spatial and temporal scales (including quality controls); and (iii) strengthen the evidence base to understand the relationship between exposure to complex chemical mixtures, biological and ecological impacts through integrated approaches and molecular data (e.g. genomics, proteomics and metabolomics). Additionally, we support the widely held view that (iv) that rather than increasing the analytical chemistry monitoring of large number of emerging contaminants, it will be important to target analytical chemistry towards key groups of chemicals of concern using effects-directed analysis. It is also important to evaluate to what extent existing biomarkers and bioassays can address various classes of emerging chemicals using the adverse outcome pathway (AOP) approach now being developed by the Organization for Economic Cooperation and Development (OECD) with respect to human toxicology and ecotoxicology.     

新疆库米什盆地硝酸盐类矿床成矿离子迁移规律及成矿模型

为了深入认识库米什盆地硝酸盐矿床成矿离子的空间分布特征、表层沉积物中硝酸盐含量较高的原因,以盆地硝酸盐矿床为研究对象,开展研究区内各类补给水样和沉积物样可溶性盐类物质化学组成的定量分析研究;结合野外地质踏勘工作,探讨研究区硝酸盐矿床成矿离子的迁移规律,初步建立盆地硝酸盐矿床沉积成矿作用模型.结果表明,K+、Na+、NO...     

吉林红旗岭1号和7号岩体中含矿超镁铁质岩的矿物化学特征:对岩浆演化过程以及铜镍硫化物矿床形成机制的约束

本文对吉林红旗岭1号和7号岩体中含矿超镁铁质岩的主要造岩矿物进行了详细研究。两岩体的主要造岩矿物为贵橄榄石、古铜辉石、单斜辉石、斜长石、角闪石和金云母。岩浆的暗色矿物结晶顺序为:橄榄石→斜方辉石→单斜辉石→角闪石→黑云母,与镜下实际观察一致,是岩浆在不同深度结晶的产物。原始岩浆来自上地幔,两岩体进入高位岩浆房中的熔体的MgO含量分别13.98%和14.22%、Mg#值分别为72.22和71.05,为含水的高镁的苦橄质玄武岩浆。深部岩浆房深度距地表约26～27km,岩浆房内的结晶温度介于1280～1379℃之间,即结晶于下地壳中。岩浆由深部上升到高位(浅部)岩浆房中的过程是近绝热的,也是快速完成的。岩浆可能经历了两次岩浆房的演化过程,岩浆在上升到高位岩浆房之前,在深部曾经历了较短时间的橄榄石和少量辉石的分离结晶作用;但在高位岩浆房中混染了地壳物质,与此同时,还经历了同源岩浆混合作用以及岩浆过冷却作用,这些都有利于岩浆体系中成矿元素含量增高以及硫达到饱和状态,使金属硫化物熔离并晶出,从而使岩体发生铜镍矿化作用。     

鲕粒成因研究的新进展

鲕粒的成因一直是一个谜一样的沉积学难题。Brehm等在2006年的实验室研究的结果表明,将鲕粒的形成可以与叠层石进行类比,是一个特殊的球状微生物席的产物,从而将鲕粒归为微生物成因。最近,来自于巴哈马现代鲕粒的研究,Duguid等在2010年认为,鲕粒形成与微生物活动不存在一个直接的关系,重新强调了鲕粒形成的化学过程,即...