新疆“帕米尔式”铁矿床成因与成矿背景分析     

张德贤  曹汇  曾敏  许明珠  李广旭  星显宏 《岩石学报》2016,32(12):3847-3864

帕米尔式"铁矿床是新疆西昆仑地区重要的磁铁矿床类型之一,其矿床地质特征、形成时代明显有别于典型的BIFs类型磁铁矿床。本文以塔什库尔干地区翁吉勒磁铁矿床和孜勒依磁铁矿床作为研究对象,通过研究其赋矿围岩和岩体的岩石地球化学特征、矿石矿相学特征、磁铁矿微量元素地球化学特征和原位Pb-Pb同位素特征,探讨了"帕米尔式"磁铁矿床的矿床成因和成矿背景。岩石地球化学研究表明翁吉勒黑云母二长花岗岩具有高SiO_2、Al_2O_3、K_2O和Na_2O。低MgO、CaO和TiO_2,而Na_2O/K_2O值变化范围很小。铝饱和指数为(1.44~1.51),显示其具有为弱过铝质岩石的特征,稀土总量富集,具有强的负Eu异常。在微量元素蛛网图上显示其富集大离子亲石元素(LILE),如K、Rb、Sr、Ba及轻稀土元素(LREE),亏损Nb、Ta,P、Ti等高场强元素。而黑云母石英片岩稀土含量亦较富集,具有中等强度的负Eu异常。低的Rb/Sr比,明显的Th、Zr、Hf、Nb、Ta,P、Ti负异常,明显的Ba正异常,显示岩石具有古大陆边缘环境的富铝沉积岩特征。翁吉勒黑云母二长花岗岩和布伦阔勒岩群黑云母石英片岩地球化学性质非常相似,表明翁吉勒黑云母二长花岗岩的形成与布伦阔勒岩群黑云母石英片岩的重熔有关。锆石LA ICP-MS定年结果表明翁吉勒黑云母二长花岗岩形成于15.0±0.3Ma和15.4±0.2Ma。磁铁矿LA ICP-MS微量元素地球化学特征表明翁吉勒铁矿床中的磁矿床中主要Si、Mn、Zn、Sn、Hf和Pb相对较高,其中Mn和Ga变化范围较大,而孜勒依铁矿床中的磁铁矿具有相对较高的亲石元素,如Mg、Al、Ti、V、Co、Ni、Ga和Sc等,其Mn和Zn含量较低且变化范围较大,其它元素变化范围均相对较窄。二者相比,翁吉勒铁矿床中的磁铁矿中微量元素变化范围相对较大,而孜勒依铁矿床中的磁铁矿变化范围较小。两个矿床的磁铁矿的原位Pb-Pb同位素存在明显的不同,两类岩石全岩Pb同位素与两个矿床中磁铁矿Pb-Pb同位素研究表明翁吉勒铁矿床中磁铁矿可能与黑云母二长花岗岩有关,为热液成因。综上所述,在塔什库尔干地区不仅存在与沉积作用有关的铁矿床,还可能存在一部分与年轻岩浆岩有关的热液型磁铁矿床。  相似文献   

南沙群岛海域长腹剑水蚤(Oithona spp.)的种类组成、数量分布及其与环境因子的关系   总被引：1，自引：0，他引：1  

杜飞雁  王亮根  王雪辉  宁加佳  谷阳光  李亚芳 《海洋与湖沼》2016,47(6):1176-1184

中小型桡足类是海洋食物网中重要的中间环节,在碳循环里细菌碳和藻类碳向高营养级转化的过程中扮演重要角色。本文通过分析2013年3—4月、6—7月、9—10月和11—12月南沙群岛海域(111°30′E—112°30′E,4°30′N—11°30′N)的生态环境调查数据,对长腹剑水蚤属(Oithona)的种类组成、数量分布及其与环境因子的关系进行了研究。结果表明:(1)南沙群岛海域共出现长腹剑水蚤15种(包括1个未定种),其中线长腹水蚤(Oithona linearis)、粗长腹剑水蚤(O.robusta)和长刺长腹剑水蚤(O.longispina)为南沙群岛海域首次记录,长腹剑水蚤属种类组成沿水深变化的现象较为明显,该属虽然在南沙群岛海域广泛分布,但单种的出现频率较低,其种类出现的季节性较强;(2)南沙群岛海域的长腹剑水蚤可以划分为常见广布组群Ⅰ和低频组群Ⅱ;(3)长腹剑水蚤年均栖息密度为30ind./m3,季节变化呈单峰型,秋季最高、冬季最低,高数量区主要出现在受南沙西部沿岸流和东部沿岸流影响的近岸海域;(4)在0—750m水深范围内,长腹剑水蚤数量沿水深梯度的垂直变化明显,呈现由浅至深数量明显减少的趋势,长腹剑水蚤主要集中分布在0—75m的水层中,75—500m数量急剧降低至最低后,在500—750m基本维持不变;(5)GAM分析表明,纬度、海水温度、盐度和叶绿素a浓度对长腹剑水蚤数量均有影响,以纬度的影响最为显著,其中长腹剑水蚤属最适温度为28.6—29.2℃,最适盐度为32.6—33.2,最适叶绿素a浓度为5—10μg/L;(6)长腹剑水蚤属更适栖息于低温和低盐,且受沿岸流影响的环境中。因此,其数量分布的季节变化与季风驱动的沿岸流势力强弱密切相关。  相似文献   

2014年春季季风间期东印度洋赤道及其邻近海域硅藻群落   总被引：3，自引：1，他引：2  

薛冰  孙军  丁昌玲  王东晓 《海洋学报》2016,38(2):112-120

2014年4月10日至5月13日在东印度洋赤道区及其邻近海域(10.08°N-6.00°S,80.00°~96.10°E)进行硅藻物种组成和群落结构的调查。分析了45个网采样品,共鉴定出浮游硅藻34属113种(包括变种、变形及未定名种),大部分物种为热带外洋性种以及暖海外洋性种,与该海区的热带及亚热带的环境特征一致。优势种为佛氏梯形藻(Climacodium frauenfeldianum)、地中海细柱藻(Leptocylindrus mediterraneus)、密聚角毛藻(Chaetoceros coarctatus)、美丽漂流藻(Planktoniella foromsa)、大西洋角毛藻那不勒斯变种(Chaetoceros atlanticus var. neapolitanus)、距端假管藻(Pseudosolenia calcar-avis,即距端根管藻Rhizosolenia calcaravis)、圆柱几内亚藻(Guinardia cylindrus)、达蒂角毛藻(Chaetoceros dadayi)、伏氏海线藻(Thalassionema frauenfeldii)、离心列海链藻(Thalassiosira excentrica)、瘤面角毛藻(Chaetoceros bacteriastroides)以及笔尖根管藻粗径变种(Rhizosolenia styliformis var. latissima)等。硅藻的平均细胞丰度为1.855×103个/m3,其平面分布不均匀,赤道断面细胞丰度较低,高值区出现在海区北部。聚类分析发现有7种生态类群,这些硅藻的种类和丰度平面分布与上层水体(200 m以浅)温度、盐度及营养盐的水柱平均值有较好的对应关系。  相似文献   

绿藻水溶性多糖的研究概况和进展   总被引：1，自引：0，他引：1  

李莎兰  洪亮  李诚博  刘晨光 《海洋科学》2016,40(9):145-151

对近年来绿藻多糖的提纯方法、组成结构及应用的研究进展进行了综述。绿藻多糖的提纯需要经过样品的前处理、提取和精制三个步骤,提取方法包括酸提、酶提、加入钙螯合剂提取、微波及超声波辅助提取。绿藻多糖是水溶性的硫酸化杂多糖。从石莼(Ulva)、浒苔(Enteromorpha)、礁膜(Monostroma)、小球藻(Chlorella)、蕨菜(Bracken)及刚毛藻(Bristles)中提取的多糖的化学组成及结构特征各不相同,而且多糖的化学组成和结构特征受提取方式的影响。绿藻多糖的生物相容性、生物可降解性及抗氧化、抗肿瘤、抗凝血、抗炎、免疫调节等多种生物活性使其在食品、医药、化妆品及农业中具有广泛的应用。有关绿藻多糖的精确结构、提纯方法及化学修饰的进一步研究将使绿藻多糖的应用更加广泛。  相似文献   

Apatite Composition of Representative Magnetite‐series and Ilmenite‐series Granitoids in Japan          下载免费PDF全文

Shunso Ishihara  Takeru Moriyama 《Resource Geology》2016,66(1):55-62

Apatites of representative magnetite‐series and ilmenite‐series granitoids were studied in the Japanese Islands. Concentrations of the volatile components F, Cl and SO₃ are differently distributed in apatites of these granitoid series. Apatites are always fluoroapatite. They have weakly higher F content in the ilmenite series than in the magnetite series. In contrast, Cl and SO₃, are significantly concentrated in apatites of the magnetite series compared to the ilmenite series. These characteristics reflect the original concentrations of these components in the host granitic magmas. A high fO₂ seems most important for the S‐concentration as sulfate in apatite of the magnetite series. REE and Y are only erratically high in the studied apatites.  相似文献   

云南磷铝石谱学特征研究   总被引：1，自引：0，他引：1  

魏中枢  狄敬如 《岩石矿物学杂志》2018,37(1):169-174

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。  相似文献   

Nature and source of the ore-forming fluids associated with orogenic gold deposits in the Dharwar Craton     

Biswajit Mishra  Kamal Lochan Pruseth  Pranjit Hazarika  Sakthi Saravanan Chinnasam 《地学前缘(英文版)》2018,9(3):715-726

Neoarchean orogenic gold deposits, associated with the greenstone-granite milieus in the Dharwar Craton include(1) the famous Kolar mine and the world class Hutti deposit;(2) small mines at HiraBuddini, Uti, Ajjanahalli, and Guddadarangavanahalli;(3) prospects at Jonnagiri; and(4) old mining camps in the Gadag and Ramagiri-Penakacherla belts. The existing diametric views on the source of ore fluid for formation of these deposits include fluids exsolved from granitic melts and extracted by metamorphic devolatilization of the greenstone sequences. Lode gold mineralization occurs in structurally controlled higher order splays in variety of host rocks such as mafic/felsic greenstones, banded iron formations, volcaniclastic rocks and granitoids. Estimated metamorphic conditions of the greenstones vary from lower greenschist facies to mid-amphibolite facies and mineralizations in all the camps are associated with distinct hydrothermal alterations. Fluid inclusion microthermometric and Raman spectroscopic studies document low salinity aqueous-gaseous(H_2O + CO_2 ± CH_4 + NaCl) ore fluids,which precipitated gold and altered the host rocks in a narrow P-T window of 0.7-2.5 kbar and 215-320℃. While the calculated fluid O-and C-isotopic values are ambiguous, S-isotopic compositions of pyrite-precipitating fluid show distinct craton-scale uniformity in terms of its reduced nature and a suggested crustal sulfur source.Available ages on greenstone metamorphism, granitoid plutonism and mineralization in the Hutti Belt are tantamount, making a geochronology-based resolution of the existing debate on the metamorphic vs.magmatic fluid source impossible. In contrast, tourmaline geochemistry suggests involvement of single fluid in formation of gold mineralization, primarily derived by metamorphic devolatilization of mafic greenstones and interlayered sedimentary rocks, with minor magmatic contributions. Similarly, compositions of scheelite, pyrite and arsenopyrite point toward operation of fault-valves that caused pressure fluctuation-induced fluid phase separation, which acted as the dominant process of gold precipitation,apart from fluid-rock sulfidation reactions. Therefore, results from geochemistry of hydrothermal minerals and those from fluid inclusion microthermometry corroborate in constraining source of ore fluid,nature of gold transport(by Au-bisulfide complex) and mechanism of gold ore formation in the Dharwar Craton.  相似文献   

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

V.V. Ryabov  O.N. Simonov  S.G. Snisar  A.A. Borovikov 《Russian Geology and Geophysics》2018,59(8):945-961

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.  相似文献   

青海湖地区生物中正构烷烃及其氢同位素组成与影响因素     

段毅  吴应忠  吴保祥  孙涛 《地质学报》2018,92(7):1541-1550

青海湖是我国最大的内陆咸水湖泊。本文应用GC-MS和GC-TC-IRMS同位素分析技术,对青海湖水生生物和周围地区陆生生物中正构烷烃及其氢同位素进行了分析,研究了生物中正构烷烃及其同位素组成。结果显示了不同生物中正构烷烃碳数分布范围在C1 5~C33之间,呈单峰型分布;主峰碳数是水生生物(除海韭菜外)相对较低,主要为C23和C25,陆生木本植物次之,为C27;陆生草本植物较高,为C27和C29;CPI值分布在4.0~29.7之间;ACL值为26.0~29.6,分布与植物类型有关。青海湖水生生物中正构烷烃氢同位素组成分布在-209.8‰~-85.6‰之间,平均值为-169.2‰~-121.2‰;陆生植物的正构烷烃δD值为-196.7‰~-84.3‰之间,平均值为-173.0‰~-108.6‰。青海湖不同水生生物和不同陆生生物之间的正构烷烃氢同位素组成差别显著。研究发现,湖泊的含盐量对水生植物的正构烷烃氢同位素具有显著影响,环境湿度和降水量明显影响了陆生植物的正构烷烃氢同位素组成;植物的正构烷烃平均氢同位素组成随着其ACL值增加,具有变轻的趋势;不同种类植物的正构烷烃合成期间具有不同的氢同位素分馏效应,与陆生植物相比较,水生植物的正构烷烃相对于环境水更富集轻氢同位素,并且随着ACL值增加,环境水和正构烷烃之间的氢同位素分馏增大。  相似文献   

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

Xuan Tang  Jinchuan Zhang  Yang Liu  Chao Yang  Qian Chen  Wei Dang  Panwang Zhao 《Chemie der Erde / Geochemistry》2018,78(1):140-151

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.  相似文献