共查询到20条相似文献，搜索用时 39 毫秒
1.
Economic important minerals and ore deposits are common in hydrothermal altered serpentinized zone. Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) satellite sensor is capable of discrimination of such hydrothermal mineralized zone and detection of hydrothermal altered minerals. In the present study, the hydrothermal altered serpentinized harzburgites of Wadi Hibi area of Northern Oman Mountains have been discriminated by using ASTER VNIR–SWIR spectral bands by image processing methods and the occurrences of Ni-magnesioferrite–magnetite–awaruite in the rocks are studied. The color composite RGB image developed using ASTER spectral bands 8, 4 and 1, mapped well the occurrence of weathered peridotites by pale green to dark blue in colors and discriminated the hydrothermally altered serpentinized rocks by pale brown to dark blue colors due to the strong absorption of OH and Mg–OH molecules that occurred in the serpentine minerals of the rocks in the study area. The ASTER band ratios 4/7, 4/1, and 2/3 × 4/3 RGB images studied are capable of discrimination of hydrothermal mineralized areas more clear by pale blue to purple colors due to the strong absorption of such hydroxyl bearing serpentine minerals. The studied image processing methods are evaluated by applying to the region of Wadi Sarami situated in the Semail ophiolite (Oman). In addition to that, the occurrence of serpentine minerals namely, lizardite and antigorite in the hydrothermally altered serpentinized region are detected qualitatively and quantitatively using Spectral Angle Mapper (SAM) supervised classification image processing method and studied.The interpreted images are verified in the field and checked for the occurrences of minerals including Ni-magnesioferrite, magnetite, pentlandite and awaruite and are confirmed through laboratory studies. Petrographic study of serpentinized harzburgites shows that the rocks consist predominantly of antigorite and lizardite serpentines, olivine and have the opaque minerals assemblage of Ni-magnesioferrite + magnetite + awaruite + pentlandite developed during serpentinization of the rock. The occurrences of such minerals are confirmed by XRD, electron microprobe analyses and spectral measurements in the laboratory.ASTER sensor proved its capability in discriminating the hydrothermal altered serpentinized zone and detecting the mineral occurrences and thus the study recommends the technique to the exploration geologists, scientists and mining geologists for mapping of such rocks and minerals in the similar arid region. 相似文献
2.
《Applied Geochemistry》2006,21(8):1301-1321
Low-quality pore waters containing high concentrations of dissolved H+, SO4, and metals have been generated in the East Tailings Management Area at Lynn Lake, Manitoba, as a result of sulfide-mineral oxidation. To assess the abundance, distribution, and solid-phase associations of S, Fe, and trace metals, the tailings pore water was analyzed, and investigations of the geochemical and mineralogical characteristics of the tailings solids were completed. The results were used to delineate the mechanisms that control acid neutralization, metal release, and metal attenuation. Migration of the low-pH conditions through the vadose zone is limited by acid-neutralization reactions, resulting in the development of distinct pore-water pH zones at depth; the neutralization reactions involve carbonate (pH ⩾ 5.7), Al-hydroxide (pH ⩾ 4.0), and aluminosilicate solids. As the zone of low-pH pore water expands, the pH will then be primarily controlled by less soluble solids, such as Fe(III) oxyhydroxides (pH < 3.5) and the relatively more recalcitrant aluminosilicates (pH ⩾ 1.3). Precipitation/dissolution reactions involving secondary Fe(III) oxyhydroxides and hydroxysulfates control the concentrations of dissolved Fe(III). Concentrations of dissolved SO4 are principally controlled by the formation of gypsum and jarosite. Geochemical extractions indicate that the solid-phase concentrations of Ni, Co, and Zn are associated predominantly with reducible and acid-soluble fractions. The concentrations of dissolved trace metals are therefore primarily controlled by adsorption/complexation and (or) co-precipitation/dissolution reactions involving secondary Fe(III) oxyhydroxide and hydroxysulfate minerals. Concentrations of dissolved metals with relatively low mobility, such as Cu, are also controlled by the precipitation of discrete minerals. Because the major proportion of metals is sequestered through adsorption and (or) co-precipitation, the metals are susceptible to remobilization if low-pH or reducing conditions develop within the tailings. 相似文献
3.
Southern Peru contains important epithermal Au–Ag (± base metals) deposits, such as Canahuire, Tucari, Santa Rosa, Caylloma, Shila and Paula. The Chapi Chiara gold prospect is located in this region and is part of a paleo-stratovolcano of the Upper Miocene–Pliocene. The hydrothermal alteration of the prospect was characterized based on spectroradiometric data, geochemistry and petrography. The mineralogical data, interpreted based on reflectance spectroscopy, were spatialized using the sequential indicator simulation technique for producing probabilistic maps of alteration. The inner part of the paleo-stratovolcano (SW sector) is marked by three main cores of advanced argillic alteration (AAA) (quartz–alunite supergroup minerals–kaolinite–dickite ± topaz ± pyrophyllite ± diaspore) associated with topographic highs. The AAA1 core is surrounded by argillic alteration (quartz–illite–paragonitic illite–smectite ± pyrite) and propylitic alteration (quartz–plagioclase–chlorite–calcite–epidote–smectite ± kaolinite ± pyrite ± chalcopyrite ± magnetite). The central sector of the prospect, situated in the NE flank of the paleo-stratovolcano, is characterized by hydrothermal breccias structured towards N65E. The main mineral phases comprise quartz and abundant pyrite, sometimes with traces of As. Anomalous geochemical values of Ag, As, Bi, Hg, Se, Sb and Te coincide with high gold contents in this sector of the prospect. Jarosite and goethite are evidence of a subsequent supergene event. Based on the mineralogical characterization, we conclude the existence of a high sulfidation epithermal system in Chapi Chiara. Hypogene minerals of higher temperature in the SW sector of the prospect, such as diaspore, pyrophyllite and topaz in the AAA zone, and epidote in the propylitic alteration zone, can reveal that the system is currently in a relatively deep erosion level, suggesting its proximity in relation to the interface between a deep epithermal system and a mesothermal system. 相似文献
4.
《Applied Geochemistry》2006,21(7):1093-1108
Peña del Hierro is an abandoned mine site located in the catchment area of the Tinto river (Pyrite Belt, SW Spain). As leaching from the spoils affect the quality of the stream water, the waste dumps have been characterized for mineralogy, geochemistry and granulometry to obtain an estimate of the potential pollution. Waste rock dumps in Peña del Hierro are very heterogeneous and are mainly composed of acid volcanic tuffs > gossan > shales > roasted pyrite ashes > floated pyrite. The volcanic tuffs, the gossan and the shales coexist in the same piles. The roasted pyrite ashes and the floated pyrite form more homogeneous dumps. The dissolution of pyrite concentrated in pyrite ashes and floated pyrite units can generate acid mine drainage. Nevertheless, acid volcanic tuffs, which are rich in pyrite and have no neutralizing minerals, are the main source of these acidic effluents. Only muscovite might partially neutralize the acidity, but the dissolution of this mineral is too slow to compensate for acidity. The occurrence of jarosite in the <2 mm fraction indicates that extreme acid mine drainage occurs. The gossan and roasted pyrite ashes have high contents of trace elements. According to their concentration, As (46–1710 ppm), Pb (113–3455 ppm) and Hg (0–53) are some of the most important toxic trace elements in these wastes. In dumps mainly composed of volcanic tuffs most of the trace elements derive from the gossan mixed in the piles. Gossan is stable in an oxidizing environment, but acidic effluents (pH < 2) can dissolve Fe oxyhydroxides from them and release high amounts of trace elements to the stream water. This research contributes to estimating the production of acid mine drainage and the actual contamination risk of potentially toxic elements in soils and waters of this area, and could be the base for possible future mitigation actions in other areas affected by mining wastes. 相似文献
5.
《Journal of South American Earth Sciences》2007,23(2-3):193-212
The latest evolution of the Neoproterozoic Agudos Grandes Batholith (Apiaí domain, SE Brazil) is marked by an important change in the type of granitic magmatism. The “late-orogenic” Piedade, Roseira, Serra dos Lopes, and Pilar do Sul granites are elliptical plutons with roughly concentric zoning and a spatial arrangement suggesting a continuous southwestward migration of the magmatic focus. The main rock types are “contaminated” calc-alkaline granites that range from mafic-rich (color index > 10), porphyritic biotite (±muscovite) granite-granodiorite in Piedade to pink, equigranular, muscovite–biotite leucogranite (CI < 5) strongly affected by hydrothermal effects in Pilar do Sul. U–Pb monazite dating indicates that these plutons were emplaced during 600–605 Ma, slightly after the main “synorogenic” magmatic stage (615–610 Ma), which was dominated by high-K, calc-alkaline, metaluminous, porphyritic hornblende-biotite granites with minor peraluminous leucogranite bodies. The “postorogenic” granites are divided into two groups on the basis of pluton shapes and U–Pb dating, both with “A-type” affinities. The approximately 585 Ma group (São Miguel Arcanjo and Capão Bonito granites) relates to the Itu granitic province, which developed around 10 m.y. after the cessation of the main regional compressional events, and cross-cuts the reworked border of the Paranapanema plate; the younger, approximately 565 Ma group is represented by two elongated plutons (Serra da Batéia and Serra da Queimada) that seem to reflect coeval orogenic events farther east in the Ribeira belt. The modal composition, magnetic susceptibility, and mafic mineral chemistry of the late-orogenic granites are consistent with an origin by contamination of metaluminous, oxidized, calc-alkaline magmas with crustal melts. 相似文献
6.
The paper describes mineralogy of the low grade metamorphosed manganese sediments, which occur in sedimentary complexes of the Pai Khoi Ridge and the Polar Urals and volcanosedimentary complexes of the Central and South Urals. The degree of metamorphism of the rocks studied corresponds to PT conditions of the prehnite–pumpellyite (deposits of Pai Khoi and Polar and South Urals) and green schist (deposits of the Central Urals) facies. One hundred and nine minerals were identified in the manganese-bearing rocks on the basis of optical and electron microscopy, X-ray diffraction, and microprobe analysis. According to the variations in the amount of major minerals of the manganese rocks of the Urals, they are subdivided on carbonate (I), oxide–carbonate–silicate (II), and oxide–silicate (III) types. Carbonates, various Mn2 +-bearing silicates associated with oxides and carbonates, and braunite (Mn3 +-bearing silicate) are the major Mn hosts in types I, II, and III, respectively. Because of the different oxidation state of Mn, the rocks of types I and II are termed as “reduced” and the rocks of type III, as “oxidized”. The formation of a certain mineralogical type of metamorphic assemblage is controlled by the content of organic matter in the primary sediments. The sequence type I → type II → type III reflects the decrease in the amount of organic matter in metalliferous sediments. Mineralogical data indicate that manganese in the primary sediments accumulated in a silicate form (MnSi gel, glass, etc). During diagenesis, the Mn–Si phase was transformed to neotokite with subsequent formation of caryopilite and further crystallization of pyroxmangite, rhodonite, tephroite, and other silicates due to reactions involving caryopilite. The hydrated Mn-silicates (caryopilite and/or friedelite) and the spatially associated parsettensite, stilpnomelane, and other minerals are the index minerals of the low grade metamorphism. Under PT conditions of prehnite–pumpellyite facies, nearly 70% of silicate minerals are hydrous. The metamorphosed Mn-bearing sediments are characterized by the low-temperature caryopilite (or tephroite-caryopilite-pyroxmangite ± rhodonite) and the high-temperature caryopilite-free (or tephroite-pyroxmangite ± rhodonite) facies. Their PT conditions correspond to zeolite and prehnite-pumpellyite (the low-temperature) and green schist and higher grade (the high-temperature) facies. 相似文献
7.
《Chemie der Erde / Geochemistry》2016,76(3):353-362
Active and abandoned mine activities constitute the sources of deterioration of water and soil quality in many parts of the world, particularly in the African Copperbelt regions. The accumulation in soils and the release of toxic substances into the aquatic ecosystem can lead to water resources pollution and may place aquatic organisms and human health at risk. In this study, the impact of past mining activity (i.e., abandoned mine) on aquatic ecosystems has been studied using ICP-MS analysis for trace metals and Rare Earth Elements (REE) in sediment samples from Lubumbashi River (RL) and Tshamilemba Canal (CT), Katanga, Democratic Republic of the Congo (DRC). Soil samples from surrounding CT were collected to evaluate trace metal and REE concentrations and their spatial distribution. The extent of trace metal contamination compared to the background area was assessed by Enrichment Factor (EF) and Geoaccumulation Index (Igeo). Additionally, the trace metal concentrations probable effect levels (PELs) for their potential environmental impact was achieved by comparing the trace metal concentrations in the sediment/soil samples with the Sediment Quality Guidelines (SQGs). Spearman's Rank-order correlation was used to identify the source and origin of contaminants. The results highlighted high concentrations of trace metals in surface sediments of CT reaching the values of 40152, 15586, 610, 10322, 60704 and 15152 mg kg−1 for Cu, Co, Zn, Pb, Fe and Mn, respectively. In the RL, the concentrations reached the values of 24093, 2046, 5463, 3340, 68290 and 769 mg kg−1 for Cu, Co, Zn, Pb, Fe and Mn, respectively. The ΣREE varied from 66 to 218 and 142–331 mg kg−1 for CT and RL, respectively. The soil samples are characterized by variable levels of trace metals. The EF analysis showed “extremely severe enrichment” for Cu and Co. However, no enrichment was observed for REE. Except for Mo, Th, U, Eu, Mo, Ho and Tm for which Igeo is classified as “moderately polluted and/or unpolluted”, all elements in different sites are classified in the class 6, “extremely polluted”. The trace metal concentrations in all sampling sites largely exceeded the SQGs and the PELs for the Protection of Aquatic Life recommendation. Cu and Co had positive correlation coefficient values (r = 0.741, P < 0.05, n = 14). This research presents useful tools for the evaluation of water contamination in abandoned and active mining areas. 相似文献
8.
The Vergenoeg fluorite deposit in the Bushveld Complex in South Africa is hosted by a volcanic pipe-like body. The distribution characteristics, composition and formation conditions of high-field-strength element (HFSE)-rich minerals in different lithological units of the deposit were investigated by optical and cathodoluminescence microscopy, scanning electron microscopy, X-ray fluorescence, inductively-coupled plasma mass-spectrometry and electron-probe microanalysis. The Vergenoeg host rocks comprise a diverse silica-undersaturated assemblage of fayalite–magnetite–fluorite with variably subordinate apatite and mineral phases enriched in rare-earth elements (REEs). The Sm–Nd isotope systematics of the fluorite from the various lithological units of the pipe support the model that the HFSE budget of the Vergenoeg pipe was likely derived from a Lebowa-type granitic magma. Isotopically, there is no evidence for other REE sources. Formation of the pipe, including development of the fluorite mineralization, occurred within the same time frame as the emplacement of other magmatic rock units of the Bushveld Complex (Sm–Nd isochron age for fluorite separates: 2040 ± 46 Ma). Hydrothermal alteration is manifested in strongly disturbed Rb–Sr isotope systematics of the Vergenoeg deposit, but did not affect its HFSE and REE budget. Whole-rock chondrite-normalized REE + Y distribution patterns of two types were observed: (i) flat patterns characteristic of magnetite–fluorite unit, gossan, metallurgical-grade fluorite (“metspar”) plugs and siderite lenses, and (ii) U-shaped patterns showing enrichment towards the heaviest REE (Tm–Lu) observed in the fayalite-rich units. Common HFSE minerals are complex Nb-rich oxides (samarskite, fergusonite), REE phosphates and fluorocarbonates. Additionally, fluocerite and REE silicates, whose identification requires further work, were found. Most of the HFSE-rich minerals are spatially associated with Fe-rich phases (e.g., pyrite, magnetite, greenalite and hematite). To a smaller extent, they are found finely disseminated or healing micro-fractures in fluorite. The whole-rock REE + Y distribution patterns of the individual lithological units are mainly controlled by the distribution of Yb-rich and Y-rich xenotime in these rocks. The common occurrence of bastnäsite-(Ce) in the gossan, “metspar” plugs and especially in the rhyolitic carapace at the pipe–wall-rock contact, controls the REE + Y distribution patterns of these rocks. HFSE minerals in the Vergenoeg pipe rocks have formed in several stages. Samarskite and coarse fluorapatite belong to the primary mineral assemblage. Fergusonite and Yb-rich xenotime formed during high- to moderate-temperature hydrothermal activity. Significant remobilization of the HFSE from the early-crystallized minerals (breakdown of fluorapatite and possibly allanite with release of REE + Y) and subsequent partial redistribution of these elements into near surface rocks are inferred. The late-stage assemblages are characterized by the presence of fine-grained REE fluorocarbonates, monazite-(Ce), monazite-(La) and xenotime-(Y). 相似文献
9.
Although the Ity deposit is the oldest operating mine in Ivory Coast, very few studies exist on this deposit. It is situated in Western Ivory Coast, some 700 km northwest of Abidjan. The mine is presently operated and mined by SMI (Société des mines d'Ity — Society of Ity Mines), and has produced one million ounces of gold since its opening in 1991. All mined ore bodies are hosted in laterite and clay formations. The gold deposits in the Ity area form a cluster of mining operations of various sizes (Flotouo, Zia, Mont Ity), hosted in a Birimian volcano-sedimentary belt. The mineralization is mostly located at the contact between a granodiorite–tonalite intrusive body and sediments. Primary gold mineralization occurs in the form of veinlets and, mostly, skarn at the contact between the granitic intrusion and limestone. Calc-silicate minerals such as diopside and andradite dominate the skarn. However, the economic gold mineralization at Ity is associated with the saprolitic zone (50–120 m thick), and consists of several mineralized lenses of clayey and ferruginous material (“Terres noires”), and of sedimentary breccia layers. A thick laterite horizon (a minimum of 10 m) overlies the saprolite and covers the land throughout the region; it is mineralized in the deposit area. This contribution provides a summary of the geological and mineralogical relationships at the Ity deposit, presents new data on skarn-type gold mineralization, and summarizes its history, from the first findings, through exploration and mining assessment. 相似文献
10.
The Pingshui Cu–Zn deposit is located in the Jiangshan–Shaoxing fault zone, which marks the Neoproterozoic suture zone between the Yangtze block and Cathaysia block in South China. It contains 0.45 million tons of proven ore reserves with grades of 1.03 wt.% Cu and 1.83 wt.% Zn. This deposit is composed of stratiform, massive sulfide ore bodies, which contain more than 60 vol.% sulfide minerals. These ore bodies are hosted in altered mafic and felsic rocks (spilites and keratophyres) of the bimodal volcanic suite that makes up the Neoproterozoic Pingshui Formation. Metallic minerals include pyrite, chalcopyrite, sphalerite, tennantite, tetrahedrite and magnetite, with minor galena. Gangue minerals are quartz, sericite, chlorite, calcite, gypsum, barite and jasper. Three distinct mineralogical zones are recognized in these massive sulfide ore bodies: a distal zone composed of sphalerite + pyrite + barite (zone I); an intermediate zone characterized by a pyrite + sphalerite + chalcopyrite assemblages (zone II); and a proximal zone containing chalcopyrite + pyrite + magnetite (zone III). A thin, layer of exhalative jaspilite overlies the sulfide ore bodies except in the proximal zone. The volcanic rocks of the Pingshui Formation are all highly altered spilites and keratophyres, but their trace element geochemistry suggests that they were generated by partial melting of the depleted mantle in an island arc setting. Homogenization temperatures of the primary fluid inclusions in quartz from massive sulfide ores are between 217 and 328 °C, and their salinities range from 3.2 to 5.7 wt.% NaCl equivalent. Raman spectroscopy of the fluid inclusions showed that water is the dominant component, with no other volatile components. Fluid inclusion data suggest that the ore-forming fluids were derived from circulating seawater. The δ34S values of pyrite from the massive sulfide ores range from − 3.6‰ to + 3.4‰, indicating that the sulfur was primarily leached from the arc volcanic rocks of the Pingshui Formation. Both pyrite from the massive sulfide ores and plagioclase from the spilites have similar lead isotope compositions, implying that the lead was also derived from the Pingshui Formation. The low lead contents of the massive sulfide ores and the geochemistry of their host rocks are similar to many VMS Cu–Zn deposits in Canada (e.g., Noranda) and thus can be classified as belonging to the bimodal-mafic subtype. The presence of magnetite and the absence of jaspilite and barite at the − 505 m level in the Pingshui deposit suggest that this level is most likely the central zone of the original lateral massive sulfide ore bodies. If this interpretation is correct, the deep part of the Pingshui Cu–Zn deposit may have significant exploration potential. 相似文献
11.
《Applied Geochemistry》2005,20(3):639-659
The oxidation of sulfide minerals from mine wastes results in the release of oxidation products to groundwater and surface water. The abandoned high-sulfide Camp tailings impoundment at Sherridon, Manitoba, wherein the tailings have undergone oxidation for more than 70 a, was investigated by hydrogeological, geochemical, and mineralogical techniques. Mineralogical analysis indicates that the unoxidized tailings contain nearly equal proportions of pyrite and pyrrhotite, which make up to 60 wt% of the total tailings, and which are accompanied by minor amounts of chalcopyrite and sphalerite, and minute amounts of galena and arsenopyrite. Extensive oxidation in the upper 50 cm of the tailings has resulted in extremely high concentrations of dissolved SO4 and metals and As in the tailings pore water (pH < 1, 129,000 mg L−1 Fe, 280,000 mg L−1 SO4, 55,000 mg L−1 Zn, 7200 mg L−1 Al, 1600 mg L−1 Cu, 260 mg L−1 Mn, 110 mg L−1 Co, 97 mg L−1 Cd, 40 mg L−1 As, 15 mg L−1 Ni, 8 mg L−1 Pb, and 3 mg L−1 Cr). The acid released from sulfide oxidation has been extensive enough to deplete carbonate minerals to 6 m depth and to partly deplete Al-silicate minerals to a 1 m depth. Below 1 m, sulfide oxidation has resulted in the formation of a continuous hardpan layer that is >1 m thick. Geochemical modeling and mineralogical analysis indicate that the hardpan layer consists of secondary melanterite, rozenite, gypsum, jarosite, and goethite. The minerals indicated mainly control the dissolved concentrations of SO4, Fe, Ca and K. The highest concentrations of dissolved metals are observed directly above and within the massive hardpan layer. Near the water table at a depth of 4 m, most metals and SO4 sharply decline in concentration. Although dissolved concentrations of metals and SO4 decrease below the water table, these concentrations remain elevated throughout the tailings, with up to 60,600 mg L−1 Fe and 91,600 mg L−1 SO4 observed in the deeper groundwater. During precipitation events, surface seeps develop along the flanks of the impoundment and discharge pore water with a geochemical composition that is similar to the composition of water directly above the hardpan. These results suggest that shallow lateral flow of water from a transient perched water table is resulting in higher contaminant loadings than would be predicted if it were assumed that discharge is derived solely from the deeper primary water table. The abundance of residual sulfide minerals, the depletion of aluminosilicate minerals in the upper meter of the tailings and the presence of a significant mass of residual sulfide minerals in this zone after 70 a of oxidation suggest that sulfide oxidation will continue to release acid, metals, and SO4 to the environment for decades to centuries. 相似文献
12.
《Russian Geology and Geophysics》2015,56(6):844-873
The Tomtor massif of Paleozoic ultramafic alkaline rocks and carbonatites is located in the northern part of the Sakha Republic (Yakutia). The massif (its total area is ~ 250 km2) is ~ 20 km in diameter, with a rounded shape and a concentrically zoned structure. The core of the massif consists of carbonatites surrounded by a discontinuous ring of ultramafic rocks and foidolites. The outer part is composed of alkali and nepheline syenites. All rocks are weathered and covered with eluvium, which is the thickest after carbonatites enriched in phosphates and REE. The weathering profile consists of four layers, from the top: kaolinite-crandallite, siderite, goethite, and francolite. The highest-grade ores are observed in the bedded deposit which fills depressions in “sagging” eluvium. The ores are laminated and cryptogranular, with high Nb, Y, Sc, and REE contents (on average, 4.5% Nb2O5, 7-10% REE2O3, 0.75% Y2O3, and 0.06% Sc2O3). The highest-grade ores are natural Nb and REE concentrates. The total REE content in some layers is > 10%. The morphologic features of the highest-grade phosphate ores from the northern part of the Burannyi site were studied. The ore-forming minerals belong to the pyrochlore group, crandallite group (goyazite), and monazite-Ce. The pyrochlore group minerals occur mainly as crystals that were completely replaced by barium-strontium pyrochlore and/or plumbopyrochlore but retained the original faces; also, they occur as numerous conchoidal fragments. The grains of the pyrochlore group minerals sometimes have a zonal structure, with an unaltered pyrochlore core and a reaction rim. Goyazite occurs predominantly as colloform grains. According to SEM and TEM data, monazite occurs in the ores as ~ 50 nm particles, which cover the outer part of halloysite tubes (800–3000 nm long and 300 nm in diameter) as a dense layer and make up peculiar biomorphic aggregates. The mineralogical data, the occurrence of biomorphic aggregates, and the close association of organic remains with ore minerals suggest that the high-grade ores of the Tomtor deposit, including the Burannyi site, resulted from a hydrothermal-sedimentary process with a presumably important role of bioaccumulation of REE phosphates. 相似文献
13.
N.A. Roslyakov M.V. Kirillov N.S. Morozova S.M. Zhmodik Yu.A. Kalinin G.V. Nesterenko N.V. Roslyakova D.K. Belyanin V.V. Kolpakov 《Russian Geology and Geophysics》2013,54(5):483-494
Holocene shallow (0.5–4.5 m, rarely more) and Pliocene–Pleistocene deep (> 25 m) placers occur within the China tectonic depression. The shallow placers are associated with the formation of the present-day drainage valleys of the China River under permafrost conditions, and the deep ones are localized within the preglacial paleovalleys of the river basin. An integrated geological and geochemical study was carried out at ten shallow commercial placers, eight of which are classified as poorly studied and “unconventional.” Placers are considered “unconventional” based on their technological characteristics (commercial gold is small (? 0.25 to + 0.1 mm), thin (? 0.1 mm), and micron-sized or “bound” (invisible)), geomorphologic conditions of formation, confinement to the oxidized zone of active permafrost, significant portion of fine hydrogenic gold, and several other minor features.The formation of shallow “unconventional” placers is controlled by the conditions of active permafrost. Under aerobic conditions, suprapermafrost waters form an oxidized zone, in which iron hydroxides impart a yellowish reddish color to water-bearing rocks. Long-lived geochemical barriers (biogenic, reduction, electrochemical, sorption, and others), including gravitational differentiation, play an important role in the concentration of small and thin gold.Alluvial deposits in Meso-Cenozoic tectonic depressions, such as the China basin, are the most promising in terms of “unconventional” placers. The main factors favoring the formation of these localities and the criteria for their assessment are large feeding sources of gold (mainly carbonaceous and sulfide) mineralization, endogenic and exogenic dispersion aureoles with thin and invisible gold; increased thickness of the suprapermafrost active layer and its temporal and spatial stability, contributing to the formation and functioning of oxidized horizons with the accumulation of ferric hydroxide and hydrogenic gold; specific morphologic varieties of hydrogenic gold, which are the fundamental criterion for primary gold mineralization with migratable metal; fine-clastic clay-rich composition of recent alluvial or alluvial-talus sediments, produced by water reworking of ancient gold-bearing weathering crusts; and development of broad floodplains filled with Holocene sediments and their junction with talus-solifluction erosional slopes. 相似文献
14.
《Applied Geochemistry》2006,21(10):1760-1780
Sulfide-rich mine tailings in Adak that are exposed to weathering cause acid mine drainage characterized by low pH (2–4) and high SO4 (up to 800 mg L−1). Surface water, sediment and soil samples collected in this study contain higher concentrations of As, Cu, Fe and Zn, compared to the target and/or intervention limits set by international regulatory agencies. In particular, high As concentrations in water (up to 2900 μg L−1) and sediment (up to 900 mg kg−1) are of concern. There is large variability in trace element concentrations, implying that both physical (grain size) and chemical factors (pH, secondary phases as sulfides, Al-oxides or clay minerals) play an important role in their distribution. The low pH keeps the trace elements dissolved, and they are transported farther downstream. Trace element partition coefficients are low (log Kd = 0.3–4.3), and saturation indices calculated with PHREEQC are <0 for common oxide and sulfidic minerals. The sediment and soil samples indicate an enhanced pollution index (up to 17), and high enrichment factors for trace elements (As up to 38,300; Zn up to 800). Finally, leaves collected from different plant types indicate bioaccumulation of several elements (As, Al, Cu, Fe and Zn). However, some of the plants growing in this area (e.g., Salix, Equisétum) are generally resistant to metal toxicity, and hence, liming and phytoremediation could be considered as potential on-site remediation methods. 相似文献
15.
《Gondwana Research》2009,15(4):569-586
This paper outlines the CHIME (chemical Th–U-total Pb isochron method) dating method, which is based on precise electron microprobe analyses of Th, U and Pb in Th- and U-bearing accessory minerals such as monazite, xenotime, zircon and polycrase. The age-mapping technique that is applicable to young monazite and zircon is also described. CHIME dating consists of analyzing multiple spots within homogeneous age domains that show sufficient compositional variation, and then these data are used to construct a “pseudo-isochron” from which an age can be obtained via regression. This method, when coupled with discrimination of possibly concordant age data by chemical criteria such as the (Ca + Si)/(Th + U + Pb + S) ratio for monazite and Ca and S contents for zircon, has the potential advantage of significant precision, and the ability to work with minerals that have a significant initial common Pb component. This technique can identify two or more homogeneous domains that are separated by age gaps smaller than the error on individual spot age analysis. Many features that are insignificant in major element analysis can have major impact in the acquisition of trace element data. Critical factors include the roles of collimator slit, detector gas, background estimation, accelerating voltage, probe current, X-ray interferences and count rate in affecting the accuracy, and a way to apply the Th and U interference correction without pure Th- and U-oxides or synthesized pure ThSiO4. The age-mapping procedure for young monazite and zircon includes acquiring PbMα (or PbMβ) intensity of individual pixels with multiple spectrometers, correcting background with background maps computed from a measured background intensity by the intensity relationships determined in advance of the measurement, calibrating of intensity with standards and calculating of ages from the Th, U and Pb concentrations. This technique provides age maps that show differences in age domains on the order of 20 Ma with in monazite as young as 100 Ma. The effect of sample damage by irradiation of intense and prolonged probe measurement is also described. 相似文献
16.
The Fairview and Sheba mines are two of the major gold mines in the Paleoarchean Barberton Greenstone Belt of Southern Africa. At these mines, gold is associated with quartz–carbonate ± rutile veins and occurs both as “invisible” gold finely dispersed in sulfides (primarily pyrite and arsenopyrite), and as visible electrum grains hosted in pyrite. Up to approximately 1000 ppm Au are contained in pyrite, and up to approximately 1700 ppm in arsenopyrite. Mapping of trace element distribution in sulfide minerals using electron microprobe and proton probe techniques revealed multiple events of ore formation and Au mineralisation. At Fairview mine, three stages of pyrite formation were identified, the last of which is associated with arsenopyrite, electrum and other sulfide minerals (sphalerite, chalcopyrite, galena, gersdorffite, and Sb-sulfides). At Sheba mine, pyrite was deposited in two stages, and electrum is associated with the second stage. At both mines, the last stage of sulfide formation is the main stage of Au deposition, and is associated with mobilisation of Au, As, Sb, Cu, Zn, and Ni. The host rock composition seems to have affected the composition of pyrite, since higher Ni and Co concentrations (up to 1.4 and 1.6 wt.%, respectively) have been measured in meta-(ultra)mafic host rocks in comparison with chert and metagreywacke. Arsenopyrite is chemically zoned, and has Sb- and S-rich cores and As- and Ni-rich rims. This zoning indicates variations in fluid compositions (decreasing Sb and increasing Ni), and crystallisation conditions (increasing As content for increasing temperature). Geothermometric estimates based on the As content of arsenopyrite (As ≤ 32 at.%) indicate temperatures up to ~ 420 °C for the crystal rims. Petrographic and cathodoluminescence observations of quartz associated with gold mineralisation show only local brittle deformation, and no plastic deformation. This supports the notion that the ore-transporting veins were emplaced late in the deformation history. Variations of cathodoluminescence of quartz are correlated with changing Al contents (Al ≤ 0.16 wt.%), and can be related to fluctuations in the pH of the mineralising fluids. 相似文献
17.
Jana Just Bernhard Schulz Helga de Wall Fred Jourdan Manoj K. Pandit 《Gondwana Research》2011,19(2):402-412
The in-situ “chemical” Th–U–Pb dating of monazite with the electron microprobe is used to unravel the Neoproterozoic tectono-thermal history of the “Erinpura Granite” terrane in the foreland of the Delhi Fold Belt (DFB) in the NW Indian craton. These granitoids are variably deformed and show effects of shearing activity. Monazites from the Erinpura granitoids recorded two main events; (1) protolith crystallization at 863 ± 23 Ma and (2) recrystallization and formation of new Th-poor monazite at 775 ± 26 Ma during shear overprint. Some components of the Erinpura granitoids, such as the Siyawa Granite and granites exposed near Sirohi town, show evidence of migmatization. This migmatization event is documented by anatexis and associated monazite crystallization at 779 ± 16 Ma. The age data indicate an overlap in timing between anatectic event and ductile shear deformation. The end of the tectono-thermal event in the Sirohi area is constrained by a 736 ± 6 Ma Ar–Ar muscovite age data from the ductile shear zone. 相似文献
18.
In this paper we show the seismicity and velocity structure of a segment of the Alpine retro-belt front along the continental collision margin of the Venetian Alps (NE Italy). Our goal is to gain insight on the buried structures and deep fault geometry in a “silent” area, i.e., an area with poor instrumental seismicity but high potential for future earthquakes, as indicated by historical earthquakes (1695 Me = 6.7 Asolo and 1936 Ms = 5.8 Bosco del Cansiglio). Local earthquakes recorded by a dense temporary seismic network are used to compute 3-D Vp and Vp/Vs tomographic images, yielding well resolved images of the upper crust underneath the south-Alpine front. We show the presence of two main distinct high Vp S-verging thrust units, the innermost coincides with the piedmont hill and the outermost is buried under a thick pile of sediments in the Po plain.Background seismicity and Vp/Vs anomalies, interpreted as cracked fluid-filled volumes, suggest that the NE portion of the outermost blind thrust and its oblique/lateral ramps may be a zone of high fluid pressure prone to future earthquakes.Three-dimensional focal mechanisms show compressive and transpressive solutions, in agreement with the tectonic setting, stress field maps and geodetic observations. The bulk of the microseismicity is clustered in two different areas, both in correspondence of inherited lateral ramps of the thrust system. Tomographic images highlight the influence of the paleogeographic setting in the tectonic style and seismic activity of the region. 相似文献
19.
Thick ferromanganese (Fe-Mn) crusts from four Cretaceous seamounts (The Paps, Tropic, Echo and Drago) at the southern Canary Island Seamount Province (CISP) in the northeastern tropical Atlantic were recovered along the flanks and summits from 1700 to 3000 m water depths. CISP is composed of > 100 seamounts and submarine hills, is likely the oldest hotspot track in the Atlantic Ocean, and is the most long-lived of known hotspots globally. The Fe-Mn crusts grow on basalt-sedimentary rock substrates below the northeastern tropical Atlantic core of the oxygen minimum zone (OMZ) with a maximum thickness of 250 mm at a water depth of 2400 m. The mineralogical and chemical composition of these Fe-Mn crusts indicate a hydrogenetic origin. The main Mn minerals are vernadite with minor interlayered todorokite and asbolane-buserite. Fe oxides are essentially ferroxyhyte and goethite. The Fe-Mn crusts show high average contents in Fe (23.5 wt%), Mn (16.1 wt%), and trace elements like Co (4700 μg/g), Ni (2800 μg/g), V (2400 μg/g) and Pb (1600 μg/g). Rare earth elements plus yttrium (REY) averages 2800 μg/g with high proportions of Ce (1600 μg/g). Total platinum group elements (PGEs) average 230 ng/g, with average Pt of 182 ng/g. Two main types of growth layers form the crusts: 1) a dense laminae of oxides with high contents in Mn, Co and Ni associated with vernadite and Cu, Ni, and Zn associated with todorokite; 2) botryoidal layers with high contents in Fe, Ti, V and REY associated with goethite. The Fe-Mn crusts from the CISP region show higher contents in Fe, V, Pb and REY but lower Mn, Co, Ni and PGEs contents than Pacific or Indian ocean seamount crusts. The oldest maximum age of initiation of crust growth was at 76 Ma (Campanian, Late Cretaceous). Using a combination of high resolution Co-chronometer and geochemical data along an Electron Probe Micro Analysis (EPMA) transect, four stages in morphology, chemical contents and growth rates can be differentiated in the the Cenozoic crusts since 28 Ma, which we interpret as due to changes in the ventilation of the North Atlantic OMZ and to the increase of Saharian dust inputs. An earliest growth period, characterized by similar contents of Fe and Mn in the interval 27.8–24.45 Ma (late Oligocene-early Miocene) reflects slow precipitation related to a thick OMZ. An intermediate laminated zone with higher contents of Fe, Si and P, high growth rates reaching 4.5 mm/Ma, and precipitation of Fe-Mn oxides during the interval 24.5–16 Ma is related to periods of ventilation of the OMZ by intrusion of deep upwelling currents. Significant increase in Fe contents at ca. 16 Ma correlates with the onset of incursions of Northern Component Waters into the North Atlantic. Finally, since 12 Ma, the very low growth rates (< 0.5 mm/Ma) of the crust are related to a thick North Atlantic OMZ, an increase in Sahara dust input and a stable thermohaline circulation. 相似文献
20.
《Chemie der Erde / Geochemistry》2017,77(1):195-206
A medium-scale shear zone exposed in the gneiss rocks of the South-western Bohemian Massif (Moldanubian Zone) contains cordierite, whose Na p.f.u. is subject to a significant increase from the centre to the edge of the deformation area, whilst other elements only show negligible variations. Coexisting mineral phases of cordierite include garnet, biotite, and sillimanite. According to the results obtained from the garnet-cordierite Fe2+/Mg2+-exchange thermometer a decrease of peak temperature from 639 °C in the central mylonite to 593 °C in the marginal mylonite can be observed, which indicates significant shear heating. Lithological pressures were estimated by considering the position of cordierite-forming reactions in the P-T field and the stability of coexisting sillimanite. They are subject to a reduction from 0.35 GPa in the highest deformed mylonite to 0.31 GPa at the margin of the shear zone. According to the results of comprehensive petrographic and mineralogical studies the investigated shear zone underwent a Variscan HT-LP metamorphic event implying the formation of cordierite and an Alpine MT-LP event entailing the rotation and decomposition of the cordierite phase. 相似文献