云南磷铝石谱学特征研究

使用电子探针、X射线粉晶衍射仪、傅里叶变换红外光谱仪、激光拉曼光谱仪、紫外可见分光光度计等仪器,对最近在云南发现的一种达到宝石级别的磷铝石进行了化学成分、矿物组成、红外吸收光谱、拉曼光谱、紫外可见吸收光谱等方面的研究。化学成分分析结果表明,该磷铝石的主要化学成分为P和Al,并含有少量的Fe和V;X射线粉晶衍射结果显示,该磷铝石的矿物成分主要为磷铝石,杂质较少;红外光谱与拉曼光谱分析均检出磷酸根基团的特征峰,红外光谱分析还显示有结晶水与结构水的存在;紫外可见吸收光谱在300和420 nm附近的吸收归属于Fe3+,630 nm附近较宽缓的吸收带由Fe3+和V3+共同产生。并将磷铝石与绿松石进行了谱学方面的对比分析,以便更好地区分两者。     

The source of sulfur in sulfide deposits in the Siberian Platform traps (from isotope data)

The source of sulfur in giant Norilsk-type sulfide deposits is discussed. A review of the state of the problem and a critical analysis of existing hypotheses are made. The distribution of δ³⁴S in sulfides of ore occurrences and small and large deposits and in normal sedimentary, metamorphogenic, and hypogene sulfates is considered. A large number of new δ³⁴S data for sulfides and sulfates in various deposits, volcanic and terrigenous rocks, coals, graphites, and metasomatites are presented. The main attention is focused on the objects of the Norilsk and Kureika ore districts. The δ³⁴S value varies from -14 to + 22.5‰ in sulfides of rocks and ores and from 15.3 to 33‰ in anhydrites. In sulfide-sulfate intergrowths and assemblages, δ³⁴S is within 4.2-14.6‰ in sulfides and within 15.3-21.3‰ in anhydrites. The most isotopically heavy sulfur was found in pyrrhotite veins in basalts (δ³⁴S = 21.6‰), in sulfate veins cutting dolomites (δ³⁴S = 33‰), and in subsidence caldera sulfates in basalts (δ³⁴S = 23.2-25.2‰). Sulfide ores of the Tsentral’naya Shilki intrusion have a heavy sulfur isotope composition (δ³⁴S = + 17.7‰ (n = 15)). Thermobarogeochemical studies of anhydrites have revealed inclusions of different types with homogenization temperatures ranging from 685 °C to 80 °C. Metamorphogenic and hypogene anhydrites are associated with a carbonaceous substance, and hypogene anhydrites have inclusions of chloride-containing salt melts. We assume that sulfur in the trap sulfide deposits was introduced with sulfates of sedimentary rocks (δ³⁴S = 22-24‰). No assimilation of sulfates by basaltic melt took place. The sedimentary anhydrites were “steamed” by hydrocarbons, which led to sulfate reduction and δ³⁴S fractionation. As a result, isotopically light sulfur accumulated in sulfides and hydrogen sulfide, isotopically heavy sulfur was removed by aqueous calcium sulfate solution, and “residual” metamorphogenic anhydrite acquired a lighter sulfur isotope composition as compared with the sedimentary one. The wide variations in δ³⁴S in sulfides and sulfates are due to changes in the physicochemical parameters of the ore-forming system (first of all, temperature and P_ch4) during the sulfate reduction. The regional hydrocarbon resources were sufficient for large-scale ore formation.     

Geochemistry of organic matter and elements of black shale during weathering in Northern Guizhou,Southwestern China: Their mobilization and inter-connection

Different from previous studies on effect of weathering upon geochemical variation along a single weathered profile, this paper provides a new methodology validated by comparing a weathered outcrop samples and their stratigraphic counterpart un-weathered core samples in a nearby shallow borehole. This outcrop and borehole penetrated the Ordovician-Silurian Wufeng–Longmaxi shales, located in the same anticline structure in the northern part of Guizhou Province, Southern China. The mineral composition, major, trace and rare earth elements (REEs) composition and Rock-Eval parameters of outcrop and core samples were analyzed and compared. Organic matter (OM) was observed in the microscope and extracted for elements analysis. The results show that short-term weathering still has significant influence on OM, mineral and elemental composition of black shales. The elements composition shows the outcrop profile was moderately weathered. The REEs compositions do not alter much during weathering process and the REEs composition and their relative ratios still are valid for rock origin determination. The OM, mainly composed by graptolite and bitumen, even entering the highly-over thermal maturity, is still sensitive to the weathering with a systematic loss 30–50% of TOC along the outcrop profile, which suggests that the OM consumption is predominantly controlled by weathering duration and the distance from the weathering surface. In turn, OM has significant influence on the trace elements transportation behavior during weathering. Some trace elements associated with the OM such as V, Cr, Th, U, Ni and Co, change significantly in their absolute concentration during weathering, but their relative ratios do not necessarily change too much and might be still reliable proxies for paleo-environmental determination. The mobility of shale minerals during weathering is in the following order: plagioclase?>?potassium feldspar and dolomite >pyrite and OM. Short-term weathering can also result in considerable transportation of elements and significant variation of minerals content in black shale, which may pose potentially high environmental and engineering risk in the regions rich in black shale.     

塔里木板块东北缘坡北杂岩体矿物成分和铂族元素特征:对硫化物熔离和构造环境的约束

坡北杂岩体位于塔里木板块东北缘北山裂谷带,主要由橄榄岩相、单辉辉石岩相、二辉岩相、辉长岩相、苏长岩相和辉长苏长岩相组成。坡一岩体中硫化物矿体赋存于超镁铁质岩中,而坡东岩体中硫化物矿体赋存于辉长苏长岩相中。坡一和坡东岩体不同岩相中单斜辉石的MgO和CaO含量、斜长石的An值和SiO_2含量连续变化且呈负相关,说明二者可能是同一原始岩浆分离结晶的产物。根据前人计算的原始岩浆成分,我们利用MELTS软件模拟了坡北杂岩体的分离结晶过程。结果表明矿物结晶顺序为:橄榄石→橄榄石+单斜辉石→橄榄石+单斜辉石+斜长石→单斜辉石+斜长石+斜方辉石,与岩相观察一致。坡北杂岩体原始岩浆经过20%分离结晶达到S饱和而发生早期硫化物熔离,形成坡一岩体中矿体。因此,在利用具有最高Fo值(90.9mol%)的橄榄石成分进行的模拟中,坡一岩体早期结晶的纯橄榄岩中橄榄石成分与分离结晶趋势线一致,而斜长橄榄岩中橄榄石成分低于趋势线,可能形成于早期硫化物熔离之后。随后岩浆中S再一次不饱和,但坡一岩体橄榄单辉辉石岩和辉长岩中橄榄石Fo和Ni含量在分离结晶趋势线之下,同时坡东岩体不含矿岩石中铂族元素总量主要在8.9×10~(-9)～29.0×10~(-9)之间,且相对于Ni和Cu明显亏损,说明在岩浆分离结晶晚期再次发生硫化物熔离,而且可能是地壳混染引起的,并形成了坡东岩体中的硫化物矿体。坡东岩体橄榄二辉岩和橄榄辉长苏长岩中橄榄石Fo值(74.5mol%～81.0mol%)较低,但变化范围较大,且Fo和Ni呈负相关关系,这可能是由于橄榄石和硫化物熔体在不平衡状态下发生成分交换造成的。坡北杂岩体超镁铁质岩石中单斜辉石Ti O2含量为0.21%～0.83%,阳离子中呈四次配位的Al(AlZ)为0.8mol%～7.8mol%,与裂谷环境堆晶岩中单斜辉石成分相似。因此,坡北杂岩体可能形成于和塔里木二叠纪地幔柱活动相关的裂谷环境。然而,超镁铁质岩石全岩Nd同位素指示其来源于亏损地幔,并不是地幔柱物质熔融的直接产物。纯橄榄岩和异剥橄榄岩La/Sm,Sm/Yb和La/Yb比值指示其源区为尖晶石二辉橄榄岩地幔。因此,坡北杂岩体源区应为浅部以尖晶石二辉橄榄岩为主的亏损岩石圈地幔,地幔柱在源区部分熔融过程中提供了大量的热。     

柴达木盆地鱼卡地区中侏罗统石门沟组砂岩碎屑组分特征及其物源构造环境分析

利用砂岩碎屑骨架成分统计和碎屑颗粒结构特征分析,研究柴达木盆地北缘鱼卡地区中侏罗统石门沟组碎屑岩的源岩类型及其构造环境。石门沟组砂岩成分成熟度中等、结构成熟度较低,具有近源物源的特点。砂岩碎屑骨架成分统计结果表明石门沟组的物源区构造背景属于再旋回造山带。结合柴达木盆地北缘中侏罗统古地理特征,确认鱼卡地区石门沟组物源区为祁连山造山带。砂岩碎屑组分可能来自于南祁连山上石炭世宗务隆山群火山岩和达肯达坂山群变质岩。     

Whole-rock chemistry of the Gameleira I uranium deposit,Lagoa Real,Brazil

The Lagoa Real uranium (U) province, referred to as Lagoa Real, is located in the state of Bahia, north-eastern Brazil. Lagoa Real has ∼112,000 metric tonnes and average grade of 2700 ppm of U₃O₈, being one of the largest U deposits in the world and the largest in Brazil. Despite its economic and strategic importance, there are gaps in the geological knowledge of the Lagoa Real U deposits. One of them is the lack of extensive whole-rock chemical data sets. Here, we present whole-rock chemical analyses for major and trace elements, including the rare-earth elements (REE), from barren country rocks to uraniferous ore shoot, systematically sampled from an exploratory drill hole. The chemical data indicate that albitite rocks, with and without uraniferous mineralisation, cannot result from sodic syenitic magmatism, as proposed by recent studies. Petrographical and geochemical evidence supports the previously suggested concept that the Lagoa Real albitite rocks resulted from sodic metasomatism of the granitic country rock, known as the São Timóteo granite. Their ore-mineral assemblages and geochemical characteristics are similar to albitite-hosted U deposits worldwide.     

鲜水河断裂带乾宁段岩石特征与内部结构及其物理-化学性质

断裂带的变形行为和断层滑移机制是目前地震研究关注的热点,断裂带岩石特征、内部结构与物理化学性质是确定断层蠕滑或粘滑行为以及断层滑移机制的基础和关键。本文以鲜水河断裂带乾宁段地表出露的断裂岩为研究对象,通过野外地质调查、室内光学显微镜、扫描电镜、粒度统计、粉末X射线衍射分析（XRD）和薄片X射线荧光光谱分析（XRF）等多种研究方法,对鲜水河断裂带岩石特征、结构构造、物性、矿物成分及化学元素分布开展了详细的分析,并探讨了相关变形行为和滑移机制。分析表明：（1）断裂带核部主要由黑色断层泥、浅黄色及黄色断层角砾岩和灰色碎裂岩、灰色断层角砾岩组成,呈单核对称结构;（2）黑色断层泥厚3~5cm,具有快速滑动结构特征,表现为断层粘滑行为。断层泥可划分出13个滑移带,最窄滑移带厚约40μm,至少代表13期古地震事件;（3）断层泥主要由伊利石、高岭石和石英等矿物组成,其中边部伊蒙混层含量异常高,为最新一次古地震的主滑移带。由于伊利石和伊蒙混层（或蒙脱石）为主要黏土矿物的断层泥渗透率低、孔隙流体压力大,以及发现断层泥楔入脉,表明地震过程中断层滑动存在热增压弱化机制;（4）从断层泥不同滑动带中碎块蚀变程度和矿物分布特征来看,地震主滑动带有向碎裂岩方向迁移的趋势。推测断层在滑动过程中,更趋向于向弱矿物含量高（如伊利石、伊蒙混层）、强矿物含量低（如方解石、高岭石）的围岩一侧迁移。     

新疆阿尔泰可可托海伟晶岩型稀有金属矿床中磷灰石地球化学特征及意义

磷灰石可以记录和保存岩浆和热液活动的信息。可可托海伟晶岩型稀有金属矿床磷灰石发育,为研究该矿床伟晶岩成岩成矿过程提供了优良的条件。已有对可可托海伟晶岩型稀有金属矿床磷灰石的研究集中在其稀土元素特征,较少讨论其对伟晶岩成岩成矿过程的制约。本文选取可可托海伟晶岩型稀有金属矿床富矿伟晶岩脉(3号脉)和相对贫矿伟晶岩脉(1号、2b号和3a号脉)中的磷灰石作为研究对象,进行磷灰石岩相学和地球化学研究。岩相学分析表明,磷灰石主要与钠长石、石英、白云母、锰铝榴石等伴生。EPMA分析显示,磷灰石F含量为3.67%～4.41%,Cl含量小于0.67%,较低的Cl含量表明伟晶岩熔体出溶的流体Cl含量较低;大部分磷灰石MnO含量为4.67%～8.71%,但2b号脉磷灰石MnO含量变化较大(1.23%～14.28%),这是由于2b号脉磷灰石具有分带结构,暗示其遭受后期热液作用,促使磷灰石溶解-再沉淀,导致MnO含量发生较大变化。LA-ICP-MS分析显示,贫矿伟晶岩脉磷灰石的稀土元素含量较低(180×10~(-6));相反,富矿伟晶岩脉磷灰石的稀土元素含量较高( 700×10~(-6)),并具有明显的四分组效应(TE_(1-3)平均值为1.7)。1号脉和3a号脉磷灰石均显示轻稀土元素富集,反映其形成过程中有含Cl热液的参与。3号脉磷灰石显示强烈Eu负异常和Ce正异常,而2b号脉磷灰石显示强烈Ce负异常和中等Eu负异常,这种Eu、Ce异常的差异可能与岩浆-热液阶段大量流体出溶密切相关。磷灰石的沉淀将导致热液中HF含量的降低,促使磷灰石周围铌钽矿结晶和Nb、Ta进入磷灰石中。可见,在伟晶岩形成过程中,磷灰石并非保持稳定,其分带结构和主微量成分变化记录了后期热液活动,暗示后期热液活动对伟晶岩的成矿具有重要作用。     

Chemical Composition of Ancient Celadon Material （1127-1279 A.D.） from Zhejiang, China and Its Implication

The microprobe EDXRF equipment was used for analysis of the major and trace elements in glaze layer-transitive layer-body layer of the celadon from the Altar Yao （Kiln） and Laohudong Yao in the Southern Song Dynasty （1127-1279 A.D.）, Zhejiang, China. The K values of the discriminant factor for the celadon wares are larger than 8, which means the celadon of the Altar Yao and Laohudong Yao are different from that of the Longquan Yao. The former two belong to the Guan Yao system （the Chinese imperial kilns）, but the latter to the Min Yao system （the Chinese popular kilns）. The principle component analysis shows their relationship between the Altar and Laohudong wares with provenance postulation. The thickness of the transitive layer in the Altar and Laohudong wares is obviously different, which reveals the microstructure characteristics of the celadon even though both kinds of wares belong to the imperial kiln system.     

斑纹鲟凝集素(CFL)的初步研究Ⅱ.CFL的分子组成及性质鉴定

采用生化方法对斑纹鲟(Charybdis feriatus)凝集素进行了初步研究.结果表明,斑纹鲟的血清中有动物红细胞和微生物细胞凝集活性的凝集素(Charybdis feriatuslectin,CFL),其活力表现依赖于Ca2+,并为多种糖所抑制;CFL对40℃以上的温度敏感,其活力在pH6.0~8.0内稳定.经巯基乙醇处理和未经巯基乙醇处理的CFL在SDS-PAGE上均为一条蛋白带,说明斑纹鲟凝集素不含二硫键,且只有一种亚基,分子量为40.8 kDa,CFL氨基酸组成分析表明其富含酸性氨基酸.