东天山白山钼矿地球化学特征及地质意义

白山钼矿赋矿岩体为花岗斑岩,其主量、微量及稀土元素地球化学特征研究表明,岩体属过铝质高钾钙碱性系列,并相对富集大离子亲石元素(Rb,Th,Sr等),亏损高场强元素(Nb,Ce,Zr等),以及具有LREE富集的右倾稀土元素分布模式。根据矿物稀土元素作为示踪剂提供的信息表明,含钼矿物的石英脉稀土元素组成和分布模式与壳幔同熔型花岗岩有众多相似之处,推测该成矿物质来源与花岗岩岩浆有关,来自同一源区,形成于碰撞后演化阶段向板内转化的构造环境,并具相同的成岩方式与成岩成矿同期。     

Early Cretaceous adakitic granites in the Northern Dabie Complex, central China: Implications for partial melting and delamination of thickened lower crust

To date, few adakitic rocks have been reported in direct association with contemporary intra-continental extensional structures, which has cast doubt on genetic models involving partial melting of the lower crust. This study presents Early Cretaceous (143-129 Ma, new Sensitive high-resolution ion microprobe (SHRIMP) zircon U-Pb ages) adakitic granites, which are directly associated with a contemporary metamorphic core complex (i.e., the Northern Dabie Complex in the Dabie area). These granites exhibit relatively high Sr contents, negligible to positive Eu and Sr anomalies, high La/Yb and Sr/Y ratios, but very low Yb and Y contents, similar to subducted oceanic crust-derived adakites. They are also characterized, however, by very low MgO or Mg^# and Ni values, and Nd-Sr isotope compositions (ε_Nd(t) = −14.6 to −19.4 and (⁸⁷Sr/⁸⁶Sr)_i = 0.7067-0.7087) similar to Triassic continent-derived eclogites subducted in the Dabie-Sulu Orogen. Additionally, late granitic dikes in the adakitic intrusions exhibit low Sr contents, clearly negative Eu and Sr anomalies, low La/Yb and Sr/Y ratios, but relatively high Yb and Y contents, similar to 118-105 Ma granites in the Northern Dabie Complex. Based on composition and geochronology data of Neoproterozoic amphibolites and orthogneisses, Triassic high- to ultra-high pressure metamorphic rocks, and Early Cretaceous mafic-ultramafic intrusive rocks, and the constraints provided by experimental melt data for tonalites, metabasaltic rocks and eclogites, we suggest that the adakitic granites were most probably generated by partial melting of thickened amphibole or rutile-bearing eclogitic lower crust as a consequence of Triassic-Middle Jurassic subduction and thrusting. The late dikes probably originated from plagioclase-bearing intermediate granulites. Moreover, we suggest that late Mesozoic delamination or foundering of thickened eclogitic lower crust is also a more plausible mechanism for the petrogenesis of Early Cretaceous mafic-ultramafic intrusive rocks in the Dabie area, and probably involved partial melting of a mixed source comprising eclogitic lower crust that had delaminated or foundered into upper lithospheric or asthenospheric mantle peridotite. Asthenospheric upwelling in response to post-collisional delamination of lithospheric mantle was likely to have provided the heat source for the Cretaceous magmatism.     

Downstream patterns of bed sediment-borne metals,minerals and organic matter in a stream system receiving acidic mine effluent: A preliminary study

Different downstream variation patterns were observed for a range of bed sediment-borne metals (aqua regia-extractable fraction) in a subtropical stream system receiving acid mine drainage. Mine-originated Fe tended to be deposited in the acidic (mean pH < 4.9) upstream reach in forms of goethite and/or hematite. In contrast, other metals tended to be transported farther downstream and settled in a low-gradient reach with high pH (mean pH > 5.6). The peak of sediment-borne Al, Be, Ca, Cd, Co, Cu, La, Mn, Ni and Zn corresponded very well with the peak of the sediment-borne organic matter, suggesting a close association between the water-borne organic colloids and the inorganic metal oxides/hydroxides during their transport. The marked increase in the sediment-borne Al and Pb started more upstream than the other metals, suggesting that the water-borne Al and Pb were more susceptible to pH rise-induced precipitation, as compared to the other metals. It appeared that the organic colloids played no important role in Pb transport and settlement. The iron precipitates had a limited role to play in affecting the transport and fates of other metals since they were predominantly formed and deposited in the acidic reach, which made them incapable of scavenging cationic metals by co-precipitation or adsorption.     

Cognate clinopyroxene from Paleogene mantle xenolith-bearing basanite lavas (East Serbia, SE Europe): the role of dissolution of mantle orthopyroxene

The study focuses on clinopyroxene from mantle xenolith-bearing East Serbian basanites and suggests that dissolution of mantle orthopyroxene played an important role in at least some stages of the crystallization of these alkaline magmas. Five compositional types of clinopyroxene are distinguished, some of them having different textural forms: megacrysts (Type-A), green/colourless-cored phenocrysts (Type-B), overgrowths and sieve-textured cores (Type-C), rims and matrix clinopyroxene (Type-D), and clinopyroxene from the reaction rims around orthopyroxene xenocrysts (Type-E). Type-A is high-Al diopside that probably crystallized at near-liquidus conditions either directly from the host basanite or from compositionally similar magmas in previous magmatic episodes. Type-B cores show high ^VIAl/^IVAl≥1 and low Mg# of mostly <75 and are interpreted as typical xenocrysts. Type-C, D and E are interpreted as typical cognate clinopyroxene. Type-D has Mg#<78, Al₂O₃?=?6–13?wt.%, TiO₂?=?1.5–4.5?wt.%, and Na₂O?=?0.4–0.8?wt.% and compositionally similar clinopyroxene is calculated by MELTS as a phase in equilibrium with the last 30?% of melt starting from the average host lava composition. Type-C has Mg#?=?72–89, Al₂O₃?=?4.5–9.5?wt.%, TiO₂?=?1–2.5?wt.%, Na₂O?=?0.35–1?wt.% and Cr₂O₃?=?0.1–1.5?wt.%. This clinopyroxene has some compositional similarities to Type-E occurring exclusively around mantle orthopyroxene. Cr/Al vs Al/Ti and Cr/Al vs Na/Ti plots revealed that Type-C clinopyroxene can crystallize from a mixture of the host basanite magma and 2–20?wt.% mantle orthopyroxene. Sieve-textured Type-C crystals show characteristics of experimentally produced skeletal clinopyroxene formed by orthopyroxene dissolution suggesting that crystallization of Type-C was both texturally and compositionally controlled by orthopyroxene breakdown. According to FeO/MgO^cpx/melt modelling the first clinopyroxene precipitating from the host basanite was Type-A (T?~?1250?°C, p?~?1.5?GPa). Dissolution of orthopyroxene produced decreasing FeO/MgO^melt and crystallization of Type-E and sieve-textured Type-C clinopyroxene (0.3–0.8?GPa and 1200–1050?°C). The melt composition gradually shifted towards higher FeO/MgO^melt ratios precipitating more evolved Type-C and Type-D approaching near-solidus conditions (<0.3?GPa; ~950?°C).     

拉斯曼丘陵新生代剥露作用的裂变径迹证据

在西南极和横贯南极山脉地区,新生代裂谷和剥露作用非常普遍。但是,文献中很少记录东南极地区的新生代剥露作用。文中根据东南极普里兹湾拉斯曼丘陵地质样品的磷灰石裂变径迹年龄和热历史的模拟,认为在东南极海岸边缘存在新生代的隆升和伸展作用,其年龄为始于(49.8±12)Ma。该年龄略晚于西南极裂谷系的启动年龄(约60~50Ma)。由于差异隆升作用,在拉斯曼丘陵地区发育了更新的正断层作用——拉斯曼丘陵拆离断层的新活动,其年龄为约5.4Ma。东南极周缘新生代裂谷和伸展作用的普遍存在,是冈瓦纳裂解以来大陆分离和印度洋形成的结果。     

Environmental Geochemistry of Mining Activities in Panzhihua Region, Southwestern China

INTRODUCTIONMining activlties have significant envi ronmenta1 inll)ac'l ssuch as visual intrusions, dust, noise, blasting, trafflc and h}'drology (Kwolek, l999; Ripley et al., l996 ). The l)rot'csst'sof mineral extraction, processing, smelting and refinlng;1rt'never approximate to the environmental neutrality, but tht' affected areas can be ameliorated (KwoIek, l999; Klukanov;1;llltlRapant, 1999). The regions, where mining activities are I,r('sent or continuous for a long tlme, are pote…     

钻井设备老化过程及规律的探讨

本文通过对钻机老化过程及规律的探讨，找出了一种方便而有效衡量钻机老化程度的数量指标，用以定量地度量钻机老化程度，为钻机发挥最佳经济效益起到一定的作用。     

Adsorption characteristics of perchloroethylene in natural sandy materials with low organic carbon content

Laboratory batch tests were conducted to investigate the sorption isotherms and sorption kinetics of the chlorinated hydrocarbon perchloroethylene (PCE) in five natural sandy materials with an organic carbon content (f _oc) in the range 0.080–0.540%. The amended non-linear dual-mode model can describe the sorption isotherms in materials with f _oc in the range 0.080–0.090%. For a sample with a much higher f _oc of 0.54%, the absorption isotherm was found to fit a linear model. These results may indicate that organic carbon is not the main factor influencing the sorption isotherm. The sorption kinetics of PCE in samples with f _oc in the range 0.080–0.090% are not first-order and are different from those observed in the samples with higher f _oc. The sorption process in the materials with lower f _oc involves fast sorption, fast desorption and an equilibrium stage. The results may imply that the factors affecting sorption kinetics of PCE in low f _oc media are pore filling and capillary condensation rather than organic carbon content.     

Iron and Sulfur Chemistry in a Stratified Lake: Evidence for Iron-Rich Sulfide Complexes

A four month study of a man-made lake used for hydroelectric power generation in northeastern Pennsylvania USA was conducted to investigate seasonal anoxia and the effects of sulfide species being transported downstream of the power generation equipment. Water column analyses show that the system is iron-rich compared to sulfide. Total Fe(II) concentrations in the hypolimnion are typically at least twice the total sulfide levels. In situ voltammetric analyses show that free Fe(II) as [Fe(H₂O)₆]²⁺ or free H₂S as H₂S/HS^- are either not present or at trace levels and that iron-rich sulfide complexes are present. From the in situ data and total Fe(II) and H₂S measurements, we infer that these iron-rich sulfide complexes may have stoichiometries such as Fe₂SH³⁺ (or polymeric forms of this and other stoichiometries). These iron-rich sulfide complexes appear related to dissolution of the iron-rich FeS mineral, mackinawite, because IAP calculations on data from discrete bottle samples obtained from bottom waters are similar to the pK_sp of mackinawite. Soluble iron-sulfide species are stable in the absence of O₂ (both in lake waters and the pipeline) and transported several miles during power generation. However, iron-sulfide complexes can react with O₂ to oxidize sulfide and can also dissociate releasing volatile H₂S when the waters containing them are exposed to the atmosphere downstream of the powerplant. Sediment analyses show that the lake is rich in oxidized iron solids (both crystalline and amorphous). Fe concentrations in FeS solids are low (<5 μmole/gr_{dry wt}) and the pyrite concentration ranges from about equal to the solid FeS to 30 times the solid FeS concentration. The degree of pyritization is below 0.12 indicating that pyrite formation is limited by free sulfide, which can react with the iron-rich sulfide complexes.     

黑龙江七星河含煤盆地古近纪-新近纪沉积相及层序地层特征

黑龙江省东部七星河盆地是一新生代聚煤盆地,其含煤地层为古近系宝泉岭组、新近系富锦组。宝泉岭组由各级砂岩、泥岩、炭质泥岩以及褐煤组成,发育滨浅湖相、深-半深湖相、三角洲平原相,属于湖泊沉积体系、三角洲沉积体系。富锦组主要由泥岩、粉砂岩、中砂岩、含砾粗砂岩及煤层、炭质泥岩、硅藻岩组成,发育滨浅湖相、扇三角洲平原相,分别属于湖泊沉积体系和扇三角洲沉积体系。层序SI相当于宝泉岭组,发育低位体系域、湖侵体系域和高位体系域,煤层主要发育高位体系域中后期,成煤环境以滨浅湖淤积沼泽为主。层序SII相当于富锦组,主要发育湖侵体系域、高位体系域,局部地区发育低位体系域,煤层亦主要发育高位体系域中后期,成煤环境以扇三角洲淤积沼泽和滨浅湖淤积沼泽为主。层序SI、SII的高位体系域中后期,盆地基底沉降速率和物源供给处于相对平衡状态,主要发育了扇三角洲淤积沼泽、滨浅湖和滨浅湖淤积沼泽环境,发育可采煤层。