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The petrography and mineral chemistry of magnetite from fifteen volcanogenic massive sulfide (VMS) deposits in Canada, and the Lasail VMS deposit in Oman, as well as from two VMS-associated banded iron formations (BIF), Austin Brook (New Brunswick, Canada) and Izok Lake (Nunavut, Canada), were investigated using optical microscopy, electron probe micro-analyzer (EPMA), and laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS). The method of robust estimation for compositional data (robCompositions) was applied to investigate geochemical censored data. Among thirty-seven elements analyzed by EPMA and/or LA-ICP-MS in magnetite from the studied deposits/bedrock lithologies, only the results for Si, Ca, Zr, Al, Mg, Ti, Zn, Co and Ni contain < 40% censored values, and thus could be imputed using robCompositions. Imputed censored data were transformed using centered log-ratios to overcome the closure effect on compositional data. Transformed data were classified by partial least squares-discriminant analysis (PLS-DA) to identify different compositional characteristics of magnetite from VMS deposits and BIFs. The integration of petrography and mineral chemistry identifies three types of magnetite in VMS settings: magmatic, hydrothermal, and metamorphic. Magmatic magnetite in VMS deposit host bedrocks is characterized by ilmenite exsolution and may be overprinted by metamorphism. Some VMS deposits contain hydrothermal magnetite, which is intergrown with sulfides, and shows a metamorphic overprint as it is partly replaced by common metamorphic minerals including chlorite, sericite, anthophyllite, and/or actinolite, whereas the majority of the deposits are characterized by metamorphic magnetite formed by replacing pre-existing sulfides and/or silicates, and is intergrown with metamorphic minerals. Among VMS deposits of the Noranda mining district, the West Ansil deposit is characterized by hydrothermal-metamorphic magnetite zoned by inclusion-free cores and Si- and Mg-rich rims. Magnetite from the studied VMS-associated BIFs is also metamorphic in origin. Aluminum, Ti and Zn contents of magnetite can separate BIF from the other mineralized and un-mineralized bedrock lithologies in the studied VMS settings.PLS-DA shows that variable compositions of magnetite slightly discriminate different studied deposits/bedrock lithologies. The geochemical observations suggest that the variation in magnetite chemistry from different VMS settings might be sourced from differences in: 1) the composition and temperature of parental magmas or hydrothermal fluids, 2) the composition of host bedrocks, 3) the composition of co-forming minerals, and 4) oxygen fugacity. PLS-DA distinguishes magnetite compositions from the studied VMS deposits and BIFs from that of the other ore deposit types including Ni–Cu, porphyry Cu-Mo-Au, iron oxide-copper- gold, iron oxide-apatite, and the Bayan Obo REE-Fe-Nb deposit. Magnetite from the VMS settings on average contains lower concentrations of Si, Zr, Al, Mg, Ti, Zn, Co and Ni relative to that from the other mineral deposit types. PLS-DA of magnetite data from VMS deposits and BIFs of the Bathurst mining camp as well as PLS-DA of magnetite compositions from various mineral deposit types yield discrimination models for application to mineral exploration for VMS deposits using indicator minerals in Quaternary lithified sedimentary rocks. 相似文献
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Brian Menounos Gerald Osborn John J. Clague Brian H. Luckman 《Quaternary Science Reviews》2009,28(21-22):2049-2074
We summarize evidence of the latest Pleistocene and Holocene glacier fluctuations in the Canadian Cordillera. Our review focuses primarily on studies completed after 1988, when the first comprehensive review of such evidence was published. The Cordilleran ice sheet reached its maximum extent about 16 ka and then rapidly decayed. Some lobes of the ice sheet, valley glaciers, and cirque glaciers advanced one or more times between 15 and 11 ka. By 11 ka, or soon thereafter, glacier cover in the Cordillera was no more extensive than at the end of the 20th century. Glaciers were least extensive between 11 and 7 ka. A general expansion of glaciers began as early as 8.4 ka when glaciers overrode forests in the southern Coast Mountains; it culminated with the climactic advances of the Little Ice Age. Holocene glacier expansion was not continuous, but rather was punctuated by advances and retreats on a variety of timescales. Radiocarbon ages of wood collected from glacier forefields reveal six major periods of glacier advance: 8.59–8.18, 7.36–6.45, 4.40–3.97, 3.54–2.77, 1.71–1.30 ka, and the past millennium. Tree-ring and lichenometric dating shows that glaciers began their Little Ice Age advances as early as the 11th century and reached their maximum Holocene positions during the early 18th or mid-19th century. Our data confirm a previously suggested pattern of episodic but successively greater Holocene glacier expansion from the early Holocene to the climactic advances of the Little Ice Age, presumably driven by decreasing summer insolation throughout the Holocene. Proxy climate records indicate that glaciers advanced during the Little Ice Age in response to cold conditions that coincided with times of sunspot minima. Priority research required to further advance our understanding of late Pleistocene and Holocene glaciation in western Canada includes constraining the age of late Pleistocene moraines in northern British Columbia and Yukon Territory, expanding the use of cosmogenic surface exposure dating techniques, using multi-proxy paleoclimate approaches, and directing more of the research effort to the northern Canadian Cordillera. 相似文献
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The Ni-Co-(PGE) sulfide deposits of the Thompson Nickel Belt (TNB) in Northern Manitoba, Canada are part of the fifth largest nickel camp in the world based on contained nickel; past production from the TNB deposits is 2500 kt Ni. The Thompson Deposit is located on the eastern and southern flanks of the Thompson Dome structure, which is a re-folded nappe structure formed during collision of the Trans-Hudson Orogen with the Canadian Shield at 1.9–1.7 Ga. The Thompson Deposit is almost entirely hosted by P2 member sulfidic metasedimentary rocks of the Paleoproterozoic Ospwagan Group. Variably serpentinised and altered dunites, peridotites and pyroxenites contain disseminated sulfides and have a spatial association with sediment-hosted Ni sulfides which comprise the bulk of the ore types. These rocks formed from rift-related komatiitic magmas that were emplaced at 1.88 Ga, and subsequently deformed by boudinage, thinning, folding, and stacking.Disseminated sulfide mineralization in the large serpentinised peridotite and dunite intrusions that host the Birchtree and Pipe Ni-Co sulfide deposits typically has 4–6 wt% Ni in 100% sulfide. The disseminated sulfides in the less abundant and much smaller boudinaged serpentinised peridotite and dunite bodies associated with the Thompson Deposit have 7–10 wt% Ni in 100% sulfide. The majority of Thompson Mine sulfides are hosted in the P2 member of the Pipe Formation which is a sulfidic schist developed from a shale prololith; the mineralization in the schist includes both low Ni tenor (<1 wt% Ni in sulfide) and barren sulfide (<200 ppm Ni) and a Ni-enriched sulfide with 1–18 wt% Ni in 100% sulfide. The semi-massive and massive sulfide ores show a similar range in Ni tenor to the metasediment-hosted mineralization, but there are discrete populations with maximum Ni tenors of ∼8, 11 and 13 wt% Ni in 100% sulfide. The variations in Ni tenor are related to the Ni/Co ratio (high Ni/Co correlates with high Ni tenor sulfide) and this relationship is produced by the different Ni/Co ratios in sulfides with a range in proportions of pyrrhotite and pentlandite. Geological models of the ore deposit, host rocks, and sulfide geochemical data in three dimensions reveal that the Thompson Deposit forms an anastomosing domain on the south and east flanks of a first order D3 structure which is the Thompson Dome. In detail, a series of second order doubly-plunging folds on the eastern and southern flank control the geometry of the mineral zones. The position of these folds on the flank of the Thompson Dome is a response to the anisotropy of the host rocks during deformation; ultramafic boudins and layers of massive quartzite in ductile metasedimentary rocks control the geometry of the doubly-plunging F3 structures. The envelope of mineralization is almost entirely contained within the P2 member of the Pipe formation, so the deposit is clearly folded by the first order and second order D3 structures. The sulfides with highest Ni tenor (typically >13 wt% Ni in sulfide) define a systematic trend that mirrors the configuration of the second order doubly-plunging F3 structures on the flanks of the Dome. Although moderate to high Ni tenor mineralization is sometimes localized in fold hinges, more typically the highest Ni tenor mineralization is located on the flanks of the fold structures.There is no indication of the mineralogical and geochemical signatures of sedimentary exhalative or hydrothermal processes in the genesis of the Thompson ores. The primary origin of the mineralization is undoubtedly magmatic and this was a critical stage in the development of economic mineralization. Variations in metal tenor in disseminated sulfides contained in ultramafic rock indicate a higher magma/sulfide ratio in the Thompson parental magma relative to Birchtree and Pipe. The variation in Ni tenor of the semi-massive and massive sulfide broadly supports this conclusion, but the variations in metal tenor in the Thompson ores was likely created partly during deformation. The sequence of rocks was modified by burial and loading of the crust (D2 events) to a peak temperature of 750 °C and pressure of 7.5 kbar. The third major phase of deformation (D3) was a sinistral transpression (D3 event) which generated the dome and basin configuration of the TNB. These conditions allowed for progressive deformation and reformation of pyrrhotite and pentlandite into monosulfide solid solution as pressure and temperature increased; this process is termed sulfide kinesis. Separation of the ductile monosulfide solid solution from granular pentlandite would result in an effective separation of Ni during metamorphism, and the monosulfide solid solution would likely be spread out in the stratigraphy to form a broad halo around the main deposit to produce the low Ni tenor sulfide. Reformation of pentlandite and pyrrhotite after the peak D2 event would explain the broad footprint of the mineral system. The effect of the D3 event at lower pressure and temperature would have been to locally redistribute, deform, and repeat the lenses of sulfide.The understanding of the relationships between petrology, stratigraphy, structure, and geochemistry has assisted in formulating a predictive exploration model that has triggered new discoveries to the north and south of the mine, and provides a framework for understanding ore genesis in deformed terrains and the future exploration of the Thompson Nickel Belt. 相似文献
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斑岩铜矿是主要的铜资源,是矿床研究和勘查的重要目标。斑岩铜矿按其与板块构造的关系可分为2种:俯冲带斑岩铜矿和碰撞造山带斑岩铜矿,它们在成矿流体方面有很多区别,其中较大的差别是碰撞造山带斑岩铜矿的钾化蚀变带比俯冲带斑岩铜矿的钾化蚀变带强得多,且范围也相对较宽。文章简述了这2种斑岩矿床的主要地质特征,着重从流体包裹体、蚀变作用和稳定同位素研究来探讨斑铜矿床成矿流体的主要特征,包括成矿流体的成分、形成温度和压力,氢、氧、碳和硫稳定同位素组成。这两种类型的斑岩铜矿中主要发育5种包裹体:M熔体包裹体;Ⅰ液体包裹体;Ⅱ气体包裹体;Ⅲ含子矿物的多相包裹体和CO2_H2O包裹体。Ⅱ类和Ⅲ类包裹体常共存,且均一温度相似,表明成矿流体经历了不混溶和沸腾作用。在Ⅲ类含子矿物的包裹体中发现了含金属硫化物(黄铜矿、黄铁矿)和氧化物(赤铁矿、磁铁矿)子矿物。在斑岩金矿和碰撞造山带的斑岩铜矿中出现CO2_H2O包裹体,在斑岩的斑晶和一些早期石英脉的石英中可见到熔体包裹体以及熔体_流体包裹体,它们代表斑岩岩浆的样品,说明斑岩铜矿的形成经历了岩浆和热液阶段。最近的研究表明,斑岩铜矿的初始流体是中等盐度和密度的岩浆流体。这种流体在上升过程中因压力释放而发生沸腾,形成气体包裹体和含子矿物的高盐度包裹体。 相似文献
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Janet M. Hergt L. Paul Bédard Stefanie M. Brueckner Klaus Peter Jochum Kathryn L. Linge Paul J. Sylvester Michael Wiedenbeck Jon D. Woodhead 《Geostandards and Geoanalytical Research》2008,32(4):397-398
In 2005 the Geostandards and Geoanalytical Research editorial team, in the true spirit of scientific endeavour, embarked on an experiment of our own. We decided to trial a new kind of review, somewhat different from those more typically observed in journals, and one that would provide readers with a summary of analytical developments across a broad range of topics appropriate to the Earth sciences. The first contribution of this kind appeared in 2005, and reported on developments in 2003 (Hergt et al. 2005). The second, this time a biennial review, was published in 2006 and reported on highlights of the 2004 and 2005 literature (Hergt et al. 2006). Based on reprint requests, positive remarks at conferences and strong citations we consider the experiment a resounding success and proudly present here the third in this series. This comprises six individual review sections that cover the main analytical technologies and topical application fields in geoanalysis and geochemistry, including geological and environmental reference materials, ICP‐thermal and secondary ionisation‐mass spectrometry, as well as neutron activation analysis, X‐ray fluorescence and atomic absorption spectrometry. 相似文献
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L. Paul Bédard 《Geostandards and Geoanalytical Research》2008,32(4):399-403
These mature analytical techniques do not show any change in publication level from the previous two years and AAS remains dominant in terms of the number of publications. The last two years have seen fewer technical improvements than in the previous review period. Some interesting papers dealing with uncertainty and quality assurance in INAA were published during 2006–2007. It is suggested that photon activation should be reconsidered because the source of electron accelerators has recently improved. A technique to preconcentrate Se for INAA determination has also been proposed. In the case of AAS, papers on analyte preconcentration continue to be more abundant than those relating to instrumental modification. Sample preparation for AAS is also active and ultrasound‐assisted leaching shows some promising applications. There were an unusual number of reviews concerned with AAS and those important to geological samples are cited here. A technique to preconcentrate Cr in water is presented and a new device to determine As and Se is showing some potential uses. Confocal X‐ray mapping continues to show interesting developments. One group developed a technique to perform XRF inside an oyster and an interesting application of μ‐XRF mapping of sediments is presented. Determination of platinum‐group elements (at μg g1 concentrations) can be carried out very quickly with an improved XRF technique. 相似文献
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