Indicator mineralogy of kimberlite boulders from eskers in the Kirkland Lake and Lake Timiskaming areas, Ontario, Canada     

Ingrid M. Kjarsgaard  M.Beth McClenaghan  Bruce A. Kjarsgaard  Larry M. Heaman 《Lithos》2004,77(1-4):705-731

Sixteen kimberlite boulders were collected from three sites on the Munro and Misema River Eskers in the Kirkland Lake kimberlite field and one site on the Sharp Lake esker in the Lake Timiskaming kimberlite field. The boulders were processed for heavy-mineral concentrates from which grains of Mg-ilmenite, chromite, garnet, clinopyroxene and olivine were picked, counted and analyzed by electron microprobe. Based on relative abundances and composition of these mineral phases, the boulders could be assigned to six mineralogically different groups, five for the Kirkland Lake area and one for the Lake Timiskaming area. Their indicator mineral composition and abundances are compared to existing data for known kimberlites in both the Kirkland Lake and Lake Timiskaming areas. Six boulders from the Munro Esker form a compositionally homogeneous group (I) in which the Mg-ilmenite population is very similar to that of the A1 kimberlite, located 7–12 km N (up-ice), directly adjacent to the Munro esker in the Kirkland Lake kimberlite field. U–Pb perovskite ages of three of the group I boulders overlap with that of the A1 kimberlite. Three other boulders recovered from the same localities in the Munro Esker also show some broad similarities in Mg-ilmenite composition and age to the A1 kimberlite. However, they are sufficiently different in mineral abundances and composition from each other and from the A1 kimberlite to assign them to different groups (II–IV). Their sources could be different phases of the same kimberlite or—more likely—three different, hitherto unknown kimberlites up-ice of the sample localities along the Munro Esker in the Kirkland Lake kimberlite field. A single boulder from the Misema River esker, Kirkland Lake, has mineral compositions that do not match any of the known kimberlites from the Kirkland Lake field. This suggests another unknown kimberlite exists in the area up-ice of the Larder Lake pit along the Misema River esker. Six boulders from the Sharp Lake esker, within the Lake Timiskaming field, form a homogeneous group with distinct mineral compositions unmatched by any of the known kimberlites in the Lake Timiskaming field. U–Pb perovskite age determinations on two of these boulders support this notion. These boulders are likely derived from an unknown kimberlite source up-ice from the Seed kimberlite, 4 km NW of the Sharp Lake pit, since indicator minerals with identical compositions to those of the Sharp Lake boulders have been found in till samples collected down-ice from Seed. Based on abundance and composition of indicator minerals, most importantly Mg-ilmenite, and supported by U–Pb age dating of perovskite, we conclude that the sources of 10 of the 16 boulders must be several hitherto unknown kimberlite bodies in the Kirkland Lake and Lake Timiskaming kimberlite fields.  相似文献   

GEOCHEMICAL CHARACTERISTICS OF PLATINUM GROUP ELEMENTS IN JINCHUAN SUPER-LARGE SULFIDE COPPER-NICKEL DEPOSIT, JINCHANG CITY, GANSU PROVINCE, CHINA     

WANG Ruiting MAO Jingwen HE Ying WANG Dongsheng TANG Zhongli 《大地构造与成矿学(英文版)》2005,29(2):152-163

The platinum-group element geochemistry of rocks and ores from Jinchuan super-large copper-nickel sulfide deposit is systemically studied in this paper. The Cu/Pd mean ratio of Jinchuan intrusion is lower than that of original mantle magma, which indicates that these ultrabasic rocks were crystallized from magma that lost Pd in the form of melting segregation of sulfides. The PGE of the rocks show trend of partial melting, similar to that of mantle peridotite, which shows that magma formation occurs during rock-forming and ore-forming processes. The chondrite normalized PGE patterns of the rocks and ores are well related to each other, which signifies the signatures of multi-episode magmatic intrusion, melting and differentiation in the formation processes of rocks and ores. In addition, analyses about the relation between PGE and S, and study on Re-Os isotopes indicate that few contamination of the crustal substances occurred during the magmatic intrusion and the formation of deposit. However, contamination by crustal substances helps to supply part of the S for the enrichment of PGE. Meanwhile, the hydrothermal process is also advantageous for the enrichment of PGE, especially lbr Pt and Pd, due to deep melting segregation. The characteristic parameters （such as Pt/（Pt＋Pd）, （Pt＋Pd）/（Ru＋Ir＋Os）, Pd/Ir, Cu/（Ni＋Cu）, and so on.） for platinum-group elements for Jinchuan sulfide copper-nickel deposit show the same features as those for sulfide copper-nickel deposit related to basic magma, which also illustrates its original magma property representative of Mg-high tholeiite. Therefore, it is the marie （not ultramafic） magma that resulted in the formation of the superlarge sulfide copper-nickel deposit enriched in Cu and PGE. To sum up, the geochemical characteristics of platinum-group elements in rocks and ores from Jinchuan copper-nickel sulfide deposit are constrained by the continental rift tectonic environment, the parent magma features, the enriched mantel magma source, the complex metallogenesis and PGE geochemical signatures, and this would be rather significant for the study about the genetic mechanism of copper-nickel sulfide deposits.  相似文献   

An experimental study on felsic rock–artificial seawater interaction: implications for hydrothermal alteration and sulfate formation in the Kuroko mining area of Japan     

Yasumasa Ogawa  Naotatsu Shikazono  Daizo Ishiyama  Hinako Sato  Toshio Mizuta 《Mineralium Deposita》2005,39(8):813-821

Experimental studies on the interactions between artificial seawater (ASW) and fresh rhyolite, perlite and weakly altered dacitic tuff containing a small amount of smectite suggest changing cation transfer during smectite-forming processes. Initially, dissolution of K from the rocks accompanies incorporation of Mg and Ca from ASW during both earlier (devitrification stage) and later smectite formation, whereas Ca incorporated with early smectite formation redissolves with progressive reaction. Barium mobility increases toward the later smectite-forming reactions. Therefore, the large amounts of barite, anhydrite and gypsum in Kuroko ore deposits are considered to have precipitated from hydrothermal solutions derived from the interaction with previously altered felsic rocks during late smectite formation, rather than by the reaction with fresh felsic rocks.Editorial handling: D. Lentz  相似文献   

Lead-arsenic soil geochemical study as an exploration guide over the Killik volcanogenic massive sulfide deposit, Northeastern Turkey   总被引：3，自引：0，他引：3  

E. ifti  H. Kolayli  S.Tokel 《Journal of Geochemical Exploration》2005,86(1):49-59

A mountainous terrain, the eastern Pontide tectonic belt, located in northeastern Turkey, contains more than 60 known volcanogenic massive sulfide (VMS) deposits that differ in reserves (0.1–30 million tonnes) and grades. Soil geochemistry is conventionally used in exploration programs to discover concealed VMS deposits in the region. In the present study, Pb and As element pair were used as pathfinder elements to investigate the relationship of their anomalies to a completely delineated ore deposit (Killik VMS deposit) in an orientation survey that served as a natural physical model. Two hundred forty soil samples were analyzed in the present study. The two elements, which represent the opposite ends of the mobility range, revealed high contrast and overlapped each other at the location of the ore deposit due to enhancement of the anomalies by hydromorphic dispersion, which is an indication that soil samples would produce reliable results. The successful delineation of the deposit is remarkable considering the rough topography and the climatic limitations. Previously the extremely moist and temperate climate was thought to cause excessive leaching of the trace element pathfinders from the ore deposits to produce extensive anomalies usually extending away from the mineralization thus, leading to erroneous results and/or extensive anomalous areas. But the present research has shown that the method can be used effectively if the sampling and data evaluation is carefully conducted.  相似文献   

Glacial dispersal studies using indicator minerals and till geochemistry around two eastern Finland kimberlites     

M.L. Lehtonen  J.S. Marmo  A.J. Nissinen  B.S. Johanson  L.K. Pakkanen 《Journal of Geochemical Exploration》2005,87(1):19-43

Diamondiferous kimberlites occur in eastern Finland, in the areas of Kaavi–Kuopio and Kuhmo. Active diamond exploration has been ongoing in the country for over two decades, but the Karelian craton still remains under explored given its size and potential. In order to develop techniques that can be applied to diamond exploration in glaciated terrains, the Geological Survey of Finland (GTK) carried out a detailed heavy mineral and geochemical survey of Quaternary till in 2001–2003 around two of the known kimberlitic bodies in Finland, Pipe 7 in Kaavi and Dyke 16 in Kuhmo. The mineralogical and geochemical signatures of these two kimberlites were studied in the basal till deposited down-ice from the targets. The kimberlites were selected to represent two different types in terms of shape, size, age and petrology, as well as showing contrasting country rocks and Quaternary deposits. Till samples up to 60 kg in weight were taken by excavator and by drill rig. Kimberlitic indicator mineral grains (0.25–1.0 mm) were concentrated using a GTK modified 3″Knelson Concentrator. Fine fractions (< 0.063 mm) of selected samples were analyzed by XRF and ICP-MS. The indicator grains down-ice from Pipe 7 form a well-defined fan in the basal till that can be followed for at least 2 km with a maximum concentration at 1.2 km distance from the pipe. Another kimberlitic body discovered during the study 300 m down-ice from Pipe 7 demonstrates that there are in fact at least two superimposed indicator fans. The results do not rule out the possibility of even more undiscovered kimberlitic sources in the area. In contrast, the indicator dispersal trail from Dyke 16 is shorter (1 km) and less well-defined than that at Kaavi, mainly due to the lower indicator content in the kimberlite itself and subsequently in till, as well as a large population of background chromites in till. The latter population is likely having been derived from the Archean Näätäniemi serpentinite massif and the associated ultramafic metavolcanics of the Kuhmo greenstone belt, located ca. 30 km up-ice from the sampling area. The indicator maximum at Seitaperä dyke swarm occurs immediately down-ice from the kimberlite, after which the concentration drops rapidly. Results of this study contribute to the overall understanding of the Quaternary history of the Kaavi and Kuhmo areas, and more importantly, provide key information to diamond exploration in these particular regions and also elsewhere in glaciated terrains.  相似文献   

北部湾沉积物粘土矿物分布特征及其环境意义     

何海军 《地质与勘探》2016,52(3):584-593

本文以南海北部湾SO-31沉积柱为研究对象,研究了14C年代学和粘土矿物学特征,并对部分全球气候事件进行了对比,为古环境、古气候的恢复提供基础资料,也为全球重大气候事件在该区域的响应提供信息。结果显示全新世以来地层沉积正常,平均沉积速率为0.57mm/a。粘土成分主要由蒙脱石、伊利石、高岭石和绿泥石组成,组合类型为蒙脱石-伊利石-高岭石-绿泥石型。全新世以来环境气候演变可划分为五个阶段:低温期阶段、干湿交替的寒冷气候阶段、逐渐升温阶段、干旱温暖气候阶段、湿热阶段。气候在每个阶段背景下还存在一些次级波动,总体趋势为干湿交替,温度逐渐上升。由于海域环境及矿物指标的影响,北部湾SO-31沉积柱粘土矿物记录的降温事件时间比其他指标记录的新仙女木降温事件发生时间滞后500~800a。  相似文献   

上扬子会泽地区早三叠世飞仙关组砂岩物源特征:来自重矿物铬尖晶石和碎屑锆石的限定   总被引：1，自引：0，他引：1  

张英利  王宗起  王刚  李谦  林健飞 《地质论评》2016,62(1):54-72

上扬子会泽地区早三叠世飞仙关组主要为河流相的紫红色砂岩,物源主要来自于西部和西北部。碎屑重矿物组合表明物源主要来自于岩浆岩,且重矿物中发现大量碎屑铬尖晶石和锆石。本文运用电子探针微区成分分析和碎屑锆石U-Pb测年方法,对上扬子早三叠世飞仙关组砂岩中铬尖晶石和碎屑锆石进行分析。铬尖晶石电子探针化学成分分析显示,其具有高铬、低Fe~(3+)和高TiO_2含量的特征,源岩分析指示这些铬尖晶石来源于与洋岛/板内、岛弧以及大火成岩省相关的火成岩。同时,碎屑锆石LA-ICP-MS U-Pb年龄测定表明,飞仙关组的物源主要来自于248~272Ma和715~997Ma的岩浆岩。铬尖晶石和碎屑锆石综合分析表明,248~272Ma的物源岩石具有大火成岩省玄武岩特征,主要为峨眉山玄武岩及同期基性侵入岩;715~997M的物源为洋岛/板内玄武岩类,主要为研究区周缘与新元古代苏雄组及其同期的岩浆岩;铬尖晶石指示的岛弧性质物源则可能源自1000~1100Ma的岩浆岩。同时,碎屑锆石还指示古元古代和早寒武世发育岩浆作用,且存在古老的新太古代结晶基底。这些资料为上扬子地区构造演化提供了沉积学的证据。  相似文献   

Characterisation of carbonate minerals from hyperspectral TIR scanning using features at 14 000 and 11 300 nm     

D. Green  M. Schodlok 《Australian Journal of Earth Sciences》2016,63(8):951-957

Rapid characterisation of carbonate phases in hyperspectral reflectance spectra acquired from drill core material has important implications for mineral exploration and resource modelling. Major infrared active features of carbonates lie in the thermal region around 6500 nm, 11 300 nm and 14 000 nm, with the latter two features being most useful for differentiating mineral species. A scatter diagram of the wavelength of the 14 000 nm feature vs that of the 11 300 nm feature, powerfully differentiates carbonates. Although the wavelength of the 11 300 nm peak is easily measured, the 14 000 nm trough and peak are commonly weak and their wavelengths can confidently be used only after filtering the spectra, e.g. selecting only those with the trough and peak separated by 175–230 nm, typical of common carbonates. The method is demonstrated with drillhole 120R from the Rosebery polymetallic VHMS deposit in western Tasmania, which has been scanned with the HyLogger-3 system. A 14 000–11 300 plot shows a high degree of clustering of the drillhole 120R data close to the library spectra of calcite, dolomite, Fe-dolomite, ankerite, kutnohorite, rhodochrosite, Fe-rhodochrosite and siderite. The interpreted compositions of the carbonate spectral populations strongly correlate with the chemical populations of 144 analysed carbonates and provide a highly resolved spatial framework for interpreting carbonate alteration.  相似文献   

Hydrogen sulfide measurements in air by passive/diffusive samplers and high-frequency analyzer: A critical comparison     

《Applied Geochemistry》2016

In this study, hydrogen sulfide (H₂S) measurements in air carried out using (a) passive/diffusive samplers (Radiello^® traps) and (b) a high-frequency (60 s) real-time analyzer (Thermo^® 450i) were compared in order to evaluate advantages and limitations of the two techniques. Four different sites in urban environments (Florence, Italy) and two volcanic areas characterized by intense degassing of H₂S-rich fluids (Campi Flegrei and Vulcano Island, Italy) were selected for such measurements. The concentrations of H₂S generally varied over 5 orders of magnitude (from 10⁻¹–10³ μg/m³), the H₂S values measured with the Radiello^® traps (H₂S_R) being significantly higher than the average values measured by the Thermo^® 450i during the trap exposure (H₂S_Ta), especially when H₂S was <30 μg/m³. To test the reproducibility of the Radiello^® traps, 8 passive/diffusive samplers were contemporaneously deployed within an 0.2 m² area in an H₂S-contaminated site at Mt. Amiata (Tuscany, Italy), revealing that the precision of the H₂S_R values was ±49%. This large uncertainty, whose cause was not recognizable, is to be added to that related to the environmental conditions (wind speed and direction, humidity, temperature), which are known to strongly affect passive measurements. The Thermo^® 450i analyzer measurements highlighted the occurrence of short-term temporal variations of the H₂S concentrations, with peak values (up to 5732 μg/m³) potentially harmful to the human health. The Radiello^® traps were not able to detect such temporal variability due to their large exposure time. The disagreement between the H₂S_R and H₂S_Ta values poses severe concerns for the selection of an appropriate methodological approach aimed to provide an accurate measurement of this highly toxic air pollutant in compliance with the WHO air quality guidelines. Although passive samplers may offer the opportunity to carry out low-cost preliminary surveys, the use of the high-frequency H₂S analyzer is preferred when an accurate assessment of air quality is required. In fact, the latter provides precise real-time measurements for a reliable estimation of the effective exposure to hazardous H₂S concentrations, giving insights into the mechanisms regulating the dispersion of this air pollutant in relation to the meteorological parameters.  相似文献   

云南会泽铅锌矿床分散元素的富集机制——兼论浅色闪锌矿富集Cd的原因          下载免费PDF全文

张茂富  周宗桂  熊索菲  宫勇军  姚书振  李行 《地质找矿论丛》2016,31(1):18-28

文章对云南会泽铅锌矿床的黄铁矿、方铅矿和闪锌矿中的分散元素进行了电子探针分析(EMPA),探讨了分散元素的富集机制.结果表明,分散元素含量已达到综合利用指标,且富集规律为:分散元素以类质同象的形式赋存,黄铁矿中分散元素含量较低,而方铅矿中分散元素的含量稍高于闪锌矿.闪锌矿中:Cd富集顺序为红色＞杂色＞黑色,在高温阶段Cd置换Fe,低温阶段Cd置换Zn;Ga通过置换Zn进入闪锌矿,Ge可能主要替代Fe而进入闪锌矿晶格.方铅矿中:Cd和Ga元素置换Fe或Pb先进入方铅矿晶格内,Ge则富集较晚,具体表现为:当Ga含量较低时,元素进入方铅矿品格顺序为Fe,Zn→Cd→Ga,Ge,当Ga含量较高时,元素进入方铅矿品格的顺序依次为Cd,Ga→Ge.  相似文献