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1.
Argentian mercurian gold,golden-yellow in colour,is a variety of native gold containing Ag and Hg,coccurring as hexagonal and tetragonal crystals in hairy,milk-droplet or irregular forms.Its microhardness Hv=91kg/mm^2,equivalent to 3.04on Mons‘scale,and the reflectance is 70.35%(589nm).Chemical analysis gave:Au 56.05-67.33,Ag18.29-31.06 and Hg 10-14.82%,as well as minor Cu.In a few samples Bi or Fe was also detected.The simplified formula is (Au0.52Ag0.36Hg0.09Cu0.02)0.99.X-ray analysis suggests the mineral is of isometric system,with space group=Oh^5-Fm3m,a0=0.40803nm,V=0.06739nm^3,and Z=4.Argentian mercurian gold occurs in a Ag-multimetal deposit at Xiacun,Baiyu County,Sichuan Province,As observed in the mining district,the mineral is distributed along the fissures of the main metallic minerals pyrite,tetrahedrite,chalcopyrite,arsenopyrite,galena,sphalerite,etc.,or in the sulfide veinlets developed in the.fissures of these minerals.Also found in the mineral deposit are native gold,argentite,sulvanite,bournonite,boulangrite,etc.  相似文献   

2.
Using the methods of electron spectroscopy of the surface and SEM–EDS, it is shown that native gold of the deposit related to the epithermal Au–Ag ore formation contains oxidized gold with an oxidation degree of Au (I) or higher on the surface. A thin layer (~15 nm) with high concentrations of Ag and S and an underlying SiO2-bearing layer with a thickness of ~30–60 nm play a protective role providing preservation of Ag and Au sulfides in the surface parts of the Au–Ag grains under the oxidizing conditions. S-rich marginal parts of native gold particles may be represented by solid solutions Ag2–xAu x S or (with a lack of S) by agglomerates of Ag n Au m S clusters. The formation of surface zoning in the nanoscale on the surface of native Au is abundant in nature and may be applied in prospecting.  相似文献   

3.
《Applied Geochemistry》1999,14(2):147-158
This study evaluates several southern Appalachian Piedmont mining districts for Hg contamination in surface waters and determines potential relationships between Hg discharged from historical mining operations and site-specific physical factors. Water samples were collected from 3 fluvial systems that drain areas where Hg was used to amalgamate Au from ore during the 19th century. Each of the fluvial systems exhibit similar physical characteristics such as climate, vegetation, and rock type. Total Hg (HgT) determinations were made using cold vapour atomic fluorescence spectroscopy techniques. Concentrations of HgT in the southern Appalachian Piedmont range from 1–3 ng l−1 in waters of the Arbacoochee, Alabama, and South Mountains, North Carolina, Mining Districts to 13 ng l−1 in waters of the Dahlonega Mining District in Georgia. The correlation between HgT and total suspended solids (TSS) at the southern Appalachian sites was good with a coefficient of determination (r2) of 0.82. A clear trend between environmentally-available Fe (FeE) and HgT (r2=0.86) was also evident. The correlation between HgT and FeE most likely reflects similarities in the mechanisms that control the aqueous concentrations of both metals (i.e., the particle-reactive nature of the two elements), allowing for the sorption of Hg onto Fe-oxyhydroxides. Hence, increased loads of TSS from erosional events are probably responsible for higher stream water HgT concentrations. Vegetation at these sites, which is heavy due to the warm, humid climate of the SE, may help reduce the total amount of Hg released from contaminated mining sites to the rivers by controlling erosion, hence, decreasing the input of contaminated particles into streams and rivers.These southern Appalachian mining sites used Hg amalgamation techniques similar to those used in other precious metals mining districts, such as the highly contaminated Comstock Au–Ag district in Nevada, yet HgT concentrations are orders of magnitude lower; This difference in concentration between the southern Appalachian districts and the Comstock district may correlate to the relative amounts of Hg that were used in each. However, other variables were evaluated to determine if physio-chemical differences such as climate could influence HgT concentrations in surface waters of the two areas.  相似文献   

4.
Detailed mineralogical and geochemical studies of the volcanogenic sulphide mineralization in the Spanish part of the Iberian Pyrite Belt (IPB) define two geochemical, mineralogical and spatial gold associations: (1) the Tharsis-Sotiel-Migollas type in which the gold is enriched with (Co?±?Bi) in the stockworks and interaction zones at the base of the massive sulphide mound; and (2) the Rio Tinto-Aznalcóllar-La Zarza type in which the gold is enriched in facies with a polymetallic (Zn?+?Ag?±?As?±?Tl?±?Hg) signature in a distal position or blocked beneath the massive sulphides. The first type is localized within a domain covering the southern half of the belt which is characterized by an abundance of sedimentary facies. The paragenesis shows that the gold association formed at high temperature (>300?°C) during the initial phases of massive sulphide genesis; the gold, which occurs in patches of very auriferous electrum (Au?>?75?wt.%), was transported by chloride complexes. The second type is found in the northern domain of the belt where volcanic facies are predominant. The paragenesis shows that the gold association formed at lower temperature (<280?°C) late in the massive sulphide genesis. This gold was transported by bisulphide complexes [Au(HS)2 ?] and is contained in Ag- and Hg-rich electrum (up to 61.0 and 30.5?wt.% respectively) and/or auriferous arsenopyrite (mean of 280?ppm Au), two mineral expressions that are able to coexist. It would appear that sulphur activity and oxygen fugacity were important factors in controlling the distribution of gold between the two host minerals and also in determining the Ag content of the electrum. This antithetic behaviour of the gold in the IPB reflects differences in the gold mineralizing fluids that may be due to the geologic environment; i.e. either dominantly sedimentary and acting as a mechanical barrier for gold bearing fluids, or dominantly volcanic and more open to seawater circulation. The fact that possible complications can occur during massive sulphide genesis, in response to the source and evolution of the fluids, raises the question of whether one or two gold influxes are involved. For example, the two gold associations could derive from a single gold influx, with remobilization and redistribution of the gold from the early (Co?±?Bi) facies giving rise to the later gold paragenesis of the (Zn?+?Ag?±?As?±?Tl?±?Hg) facies; this would not have occurred or would have been limited at the Tharsis-Sotiel-Migollas type orebodies. Alternatively, the two gold associations could reflect two separate evolutionary processes distinguished by the gold appearing either early or late in the hydrothermal fluids. Knowing the gold association of a massive sulphide deposit is an advantage when exploring for potential host facies.  相似文献   

5.
《Applied Geochemistry》2006,21(11):1969-1985
Gossan Creek, a headwater stream in the SE Upsalquitch River watershed in New Brunswick, Canada, contains elevated concentrations of total Hg (HgT up to 60 μg/L). Aqueous geochemical investigations of the shallow groundwater at the headwaters of the creek confirm that the source of Hg is a contaminated groundwater plume (neutral pH with Hg and Cl concentrations up to 150 μg/L and 20 mg/L, respectively), originating from the Murray Brook mine tailings, that discharges at the headwaters of the creek. The discharge area of the contaminant plume was partially delineated based on elevated pH and Cl concentrations in the groundwater. The local groundwater outside of the plume contains much lower concentrations of Hg and Cl (<0.1 μg/L and 3.8 mg/L, respectively) and displays the chemical characteristics of an acid-sulfate weathering system, with low pH (4.1–5.5) and elevated concentrations of Cu, Zn, Pb and SO4 (up to 5400 μg Cu/L, 8700 μg Zn/L, 70 μg Pb/L and 330 mg SO4/L), derived from oxidation of sulfide minerals in the Murray Brook volcanogenic massive sulfide deposit and surrounding bedrock. The HgT mass loads measured at various hydrologic control points along the stream system indicate that 95–99% of the dissolved HgT is attenuated in the first 3–4 km from the source. Analyses of creek bed sediments for Au, Ag, Cu, Zn, Pb and Hg indicate that these metals have partitioned strongly to the sediments. Mineralogical investigations of the contaminated sediments using analytical scanning electron microscopy (SEM), transmission electron microscopy (TEM) and scanning transmission electron microscopy (STEM), reveal discrete particles (<1–2 μm) of metacinnabar (HgS), mixed Au–Ag–Hg amalgam, Cu sulfide and Ag sulfide.  相似文献   

6.
The mineral and geochemical compositions of noble-metal (first of all, gold) deposits of the Fennoscandian, Siberian, and Northeast Asian orogenic belts are considered. These deposits are of several types: Au (disseminated Au–sulfide and Au–quartz), Au–Bi, Au–Ag, Au–Sb, Ag–Sb, Au–Sb–Hg, and Ag–Hg. They formed in different geodynamic settings as a result of the active motion of crustal tectonic blocks of different nature. Subduction processes (both at the front and at the rear of continent-marginal and island-arc magmatic arcs) resulted in Au–Ag, Ag–Sb, Ag–Hg, Au–Sb–Hg, and Au–Bi deposits. Collision events gave rise to Au and Au–Bi deposits. Intraplate continental rifting and formation of orogenic belts along the boundaries of block (plate) sliding led to the origin of Au and Au–Bi ores in association with Au–Ag, Au–Sb–Hg, and complex ores. In all cases, the formation of noble-metal mineralization was accompanied by magmatism of different types and metamorphism. Because of this diversity of ores, there is no single concept of the genesis of noble-metal mineralization. Several competing models of genesis exist: hydrothermal-metamorphic, pluton-metamorphic, plutonic, activity of mantle fluid flows, and multistage concentration during the crust–mantle interaction with the leading role of sedimentary complexes.  相似文献   

7.
We carried out experiments on crystallization of Fe-containing melts FeS2Ag0.1–0.1xAu0.1x (x = 0.05, 0.2, 0.4, and 0.8) with Ag/Au weight ratios from 10 to 0.1. Mixtures prepared from elements in corresponding proportions were heated in evacuated quartz ampoules to 1050 ºC and kept at this temperature for 12 h; then they were cooled to 150 ºC, annealed for 30 days, and cooled to room temperature. The solid-phase products were studied by optical and electron microscopy and X-ray spectroscopy. The crystallization products were mainly from iron sulfides: monoclinic pyrrhotite (Fe0.47S0.53 or Fe7S8) and pyrite (Fe0.99S2.01). Gold–silver sulfides (low-temperature modifications) are present in all synthesized samples. Depending on Ag/Au, the following sulfides are produced: acanthite (Ag/Au = 10), solid solutions Ag2–xAuxS (Ag/Au = 10, 2), uytenbogaardtite (Ag/Au = 2, 0.75), and petrovskaite (Ag/Au = 0.75, 0.12). They contain iron impurities (up to 3.3 wt.%). Xenomorphic micro- (<1–5 μm) and macrograins (5–50 μm) of Au–Ag sulfides are localized in pyrite or between the grains of pyrite and pyrrhotite. High-fineness gold was detected in the samples with initial ratio Ag/Au ≤ 2. It is present as fine and large rounded microinclusions or as intergrowths with Au–Ag sulfides in pyrite or, more seldom, at the boundary of pyrite and pyrrhotite grains. This gold contains up to 5.7 wt.% Fe. Based on the sample textures and phase relations, a sequence of their crystallization was determined. At ~1050 ºC, there are probably iron sulfide melt L1 (Fe,S ? Ag,Au), gold–silver sulfide melt L2 (Au,Ag,S ? Fe), and liquid sulfur LS. On cooling, melt L1 produces pyrrhotite; further cooling leads to the crystallization of high-fineness gold (macrograins from L1 and micrograins from L2) and Au–Ag sulfides (micrograins from L1 and macrograins from L2). Pyrite crystallizes after gold–silver sulfides by the peritectic reaction FeS + LS = FeS2 at ~743 ºC. Elemental sulfur is the last to crystallize. Gold–silver sulfides are stable and dominate over native gold and silver, especially in pyrite-containing ores with high Ag/Au ratios.  相似文献   

8.
Geology and mineralogy of the Ulakhan Au-Ag epithermal deposit (northeastern Russia, Magadan Region) are considered. A four-stage scheme of mineral formation sequence is proposed. Concentrations of Au and Ag in minerals of early and late parageneses were determined. It has been established that uytenbogaardtite is associated with native gold and hypergenesis stage minerals — goethite, hydrogoethite, or limonite replacing pyrite. The compositions of uytenbogaardtite (Ag3AuS2), acanthite (Ag2S), and native gold were studied. The composition of the Ulakhan uytenbogaardtite is compared with those of Au and Ag sulfides from other deposits. Thermodynamic calculations in the system H2O–Fe–Au–Ag–S–C–Na–Cl were carried out, which simulate the interaction of native gold and silver with O2- and CO2-saturated surface waters (carbonaceous, sulfide-carbonaceous, and chloride-sodium-carbonaceous) in the presence and absence of acanthite and pyrite at 25 °C and 1 bar. In closed pyrite-including systems, native silver and kustelite are replaced by acanthite; electrum, by uytenbogaardtite, acanthite, and pure gold; and native gold with a fineness of 700–900‰, by pure gold and uytenbogaardtite. Under the interaction with surface waters in the presence of Ag2S and pyrite, Au-Ag alloys form equilibrium assemblages with petrovskaite or uytenbogaardtite and pure gold. The calculation results confirmed that Au and Ag sulfides can form after native gold in systems involving sulfide-carbon dioxide solutions (H2Saq > 10–4 m). The modeling results support the possible formation of uytenbogaardtite and petrovskaite with the participation of native gold in the hypergenesis zone of epithermal Au-Ag deposits during the oxidation of Au(Ag)-containing pyrite, acanthite, or other sulfides.  相似文献   

9.
Shuiyindong is one of the largest and highest grade stratabound Carlin-type gold deposits in China. This paper reports on the results of petrographic studies, electron microprobe analyses (EMPA) of arsenian pyrite, and the mass transfer during mineralization and alteration, and it presents the deposit-scale distributions of Au, As, Sb, Hg, Tl, and trace elements in a representative cross section across the Shuiyindong Carlin-type gold deposit, Guizhou Province. The main objectives were to identify the precipitation mechanisms of minerals, or elements from fluids, and the migration paths of ore-forming fluids.Petrographic and EMPA studies indicate that gold in the primary ores is mainly hosted by arsenian pyrite. Mass transfer associated with alteration and mineralization shows that Au, As, Sb, Hg, Tl, and S were significantly added to all mineralized rocks, Fe2O3 and SiO2 were immobile in the main orebodies that are hosted in bioclastic limestone, and CaO, Na2O, Sr, and Li were removed from country rocks. The relations between Fe and S indicate that the sedimentary rocks at the Shuiyindong deposit contain more iron than is needed to combine with all of their contained sulfur to form pyrite. This suggests that sulfidation and decarbonation were the principal mechanism of gold precipitation at the Shuiyindong deposit. Hg, Sb, and As commonly formed sulfide minerals, such as stibnite, realgar, and orpiment, in late-stage quartz–calcite veins, or absorbed by organic matter in argillite. Fluid cooling presumably led to depositions of stibnite, realgar, and orpiment in late-stage quartz–calcite veins. Organic matter likely served as a reductant in argillite for the ore fluids, causing the precipitation of As, Sb, Hg, and S, as well as Au.Deposit-scale distributions of gold and other relevant elements reflect the passage of fluids through the rocks. Rock strata and structures allowed the ore-forming fluids to migrate horizontally along the unconformity surface of the Middle–Upper Permian, converge on the high position of an anticline, and then ascend into the overlying strata along the anticlinal axis. The distributions of the major and trace elements show that elements that accompanied the ore-forming fluids include Au, As, Sb, Hg, Tl, and S, and that Na2O and Li were exhausted in the Longtan Formation at the anticlinal core during gold mineralization. The enrichment of Co, Cr, and Ni in the Longtan Formation at the anticlinal core might be associated with deformation that formed the anticline, or with gold mineralization. Different host rocks were preferentially mineralized by different elements. The bioclastic limestone is commonly enriched in Au, whereas the argillite is preferentially enriched in As, Hg, Sb, and Tl. The zonation of ore-forming elements in the deposit appears to be Sb–Tl–As–Hg–Au–Hg–As (from bottom to top). Enrichment of Au, As, Sb, Hg, and Tl provides useful guidance for the exploration for Carlin-type gold deposits in Guizhou. Anomalies of As and Hg in soil or stream sediment might be an important clue and these elements can be used as indicator elements. Ore-forming fluids migrated along the unconformity surface of the Middle–Upper Permian and the anticlinal axis, so these are favorable sites for exploration for Carlin-type gold deposits in Guizhou.  相似文献   

10.
Mercury (Hg) and methylmercury (CH3Hg+) concentrations in streambed sediment and water were determined at 27 locations throughout the Sacramento River Basin, CA. Mercury in sediment was elevated at locations downstream of either Hg mining or Au mining activities where Hg was used in the recovery of Au. Methylmercury in sediment was highest (2.84 ng/g) at a location with the greatest wetland land cover, in spite of lower total Hg at that site relative to other river sites. Mercury in unfiltered water was measured at 4 locations on the Sacramento River and at tributaries draining the mining regions, as well as agricultural regions. The highest levels of Hg in unfiltered water (2248 ng/l) were measured at a site downstream of a historic Hg mining area, and the highest levels at all sites were measured in samples collected during high streamflow when the levels of suspended sediment were also elevated. Mercury in unfiltered water exceeded the current federal and state recommended criterion for protection of aquatic life (50 ng/l as total Hg in unfiltered water) only during high streamflow conditions. The highest loading of Hg to the San Francisco Bay system was attributed to sources within the Cache Creek watershed, which are downstream of historic Hg mines, and to an unknown source or sources to the mainstem of the Sacramento River upstream of historic Au mining regions. That unknown source is possibly associated with a volcanic deposit. Methylmercury concentrations also were dependent on season and hydrologic conditions. The highest levels (1.98 ng/l) in the Sacramento River, during the period of study, were measured during a major flood event. The reactivity of Hg in unfiltered water was assessed by measuring the amount available for reaction by a strong reducing agent. Although most Hg was found to be nonreactive, the highest reactivity (7.8% of the total Hg in water) was measured in the sample collected from the same site with high CH3Hg+ in sediment, and during the time of year when that site was under continual flooded conditions. Although Hg concentrations in water downstream of the Hg mining operations were measured as high as 2248 ng/l during stormwater runoff events, the transported Hg was found to have a low potential for geochemical transformations, as indicated by the low reactivity to the reducing agent (0.0001% of the total), probably because most of the Hg in the unfiltered water sample was in the mercury sulfide form.  相似文献   

11.
This paper is focused on the new data for geology, mineralogy, and geochemistry of stockworks consisting of steep and gentle quartz veins and veinlets forming a complex multilevel structure at the Rodion deposit. These stockworks range from 25 to 150 m in thickness. Average gold grade is 1.8 g/t. Ore minerals pyrite, arsenopyrite, chalcopyrite, sphalerite, galena, and native gold are predominantly concentrated on the vein and veinlet walls. Thermal metamorphism caused by the intrusion of the Ulakhan granodiorite pluton is the important singularity of the deposit. The deposit ore is enriched in chalcophile microelements Au, Ag, As, Sb, Cu, Pb, Zn, and Bi as compared to the average composition of the upper crust and hosting Permian sequences. The enrichment factors range from a few to hundreds of times. Bi, W, Pb, Ag, and Na2O are positively correlated between each other and with Au. The highest correlation coefficient 0.59 is between Au and Bi. Au is negatively correlated with Ba, Li, Co, Ni, Mn, Ti, and Be. The stockwork ores were formed involving homogeneous low-saline (9.4–4.3 wt % NaCl equiv) substantially aqueous bicarbonate-chloride fluid at 275–330°C and 300–1840 bar fluid pressure. Fluid has a high concentration of CO2 (up to 349 g/kg of water) and is reductive (СО2/СН4 = 17–37.3). Na and Ca are the major cations in the fluid, whereas K and Mg are minor. In addition, many microelements were detected in the fluid: As, Li, Rb, Cs, Mo, Ag, Sb, Cu, Zn, Cd, Pb, U, Ga, Ge, Ti, Mn, Fe, Co, Ni, V, Cr, Y, Zr, Sn, Ba, W, Au, Hg, and REE. The results obtained are consistent with the metamorphic–magmatic formation model of orogenic gold–quartz deposits within the Yana–Kolyma belt.  相似文献   

12.
Separated gold grains from 94 samples of the Vaal Placer, Klerksdorp gold field, South Africa have been analyzed for Au, Ag and Hg. Average gold grain compositions in these samples range from 80 to 95 weight percent Au, 4 to 18 weight percent Ag and 0.5 to 4 weight percent Hg with an average composition around Au 90, Au 8, Hg 2. Individual grains are homogeneous but significant differences exist between gold grains from single small samples and also between average compositions in separate samples. The data do not fit any simple model of gold compositional control by provenance or by metamorphic homogenization.  相似文献   

13.
The «Selektor-C» software package and standard thermodynamic functions of ternary Ag–Au–Hg solid solutions were used for developing physicochemical models in natural processes with participation of gold, silver and mercury. On the example of the Kyuchyus Au–Sb–Hg deposit we have worked out hypogene and hypergene models of formation of native gold, including mercuric gold. We obtained thermodynamic evidence that the Kyuchyus deposit ores formed with the origin of electrum at the early main productive quartz–sulfide stage and ternary Au–Ag–Hg solid solutions at the late non-substantive Au-bearing stages.  相似文献   

14.
Abstract. The Yuryang gold deposit, comprising a Te‐bearing Au‐Ag vein mineralization, is located in the Cheonan area of the Republic of Korea. The deposit is hosted in Precambrian gneiss and closely related to pegmatite. The mineralized veins display massive quartz textures, with weak alteration adjacent to the veins. The ore mineralization is simple, with a low Ag/Au ratio of 1.5:1, due to the paucity of Ag‐phases. Ore mineralization took place in two different mineral assemblages with paragenetic time; early Fe‐sulfide mineralization and late Fe‐sulfide and Au‐Te mineralization. The early Fe‐sulfide mineralization (pyrite + sphalerite) occurred typically along the vein margins, and the subsequent Au‐Te mineralization is characterized by fracture fillings of galena, sphalerite, pyrrhotite, Te‐bearing minerals (petzite, altaite, hessite and Bi‐Te mineral) and electrum. Fluid inclusions characteristically contain CO2 and can be classified into four types (Ia, Ib, IIa and IIb) according to the phase behavior. The pressure corrected temperatures (≥500d?C) indicate that the deposit was formed at a distinctively high temperature from fluids with moderate to low salinity (<12 wt% equiv. NaCl) and CH4 (1?22 mole %). The sphalerite geo‐barometry yield an estimated pressure about 3.5 ?2.1 kbar. The dominant ore‐deposition mechanisms were CO2 effervescence and concomitant H2S volatilization, which triggered sulfidation and gold mineralization. The measured and calculated isotopic compositions of fluids (δ18OH2O = 10.3 to 12.4 %o; δDH2O = ‐52 to ‐77 %o) may indicate that the gold deposition originated from S‐type magmatic waters. The physicochemical conditions observed in the Yuryang gold deposit indicate that the Jurassic gold deposits in the Cheonan area, including the Yuryang gold deposit are compatible with deposition of the intrusion‐related Au‐Te veins from deeply sourced fluids generated by the late Jurassic Daebo magmatism.  相似文献   

15.
Gold deposits of Uzbekistan are localized in the Kyzylkum, Nurata, and Kurama ore districts of the Kyzylkum-Kurama metallogenic belt. They comprise a consecutive series of deposit types corresponding to the series of geochemical associations: (Au-W)—(Au-As)—(Au-Te)—(Au-Ag)—(Au-Sb)—(Au-Hg), which are arranged as a system of zones in orebodies, deposits, ore fields, and ore districts. The distribution of chemical elements characterized by average global concentrations in the crust within the ppm-ppb (10−6-10−9 t) range was studied in ores of gold deposits using an ICP MS Elan DRC II device. Mineral nanoassemblages with a grain size of 10−6 to 10−9 m were examined with a Jeol YXA 8800R Superprobe. The Au-W, Au-As, and Au-Te associations with Bi tellurides and maldonite in ore dominate at hypo- and meso-abyssal gold deposits of the Kyzylkum district (Muruntau, Myutenbay). The contribution of the Au-Sb association with Pb, Ag, and Fe sulfoantimonites and aurostibite increases at the Daughyztau, Kokpatas, and Amantaitau gold deposits. The Au-As, Au-Te, and Au-Sb associations with Bi tellurides, maldonite, sulfoantimonites, and aurostibite dominate at the mesoabyssal gold deposits of the Nurata district (Charmitan, Guzhumsay). The Au-Te and Au-Ag associations with Au, Ag, Pb, Sb, Bi, and Hg tellurides and Bi selenides dominate at the hypabyssal gold deposits of the Kurama district (Kochbulak, Kayragach). The gold-silver deposits of the Kyzylkum district (Kosmanachi, Vysokovol’tnoe) and the Kurama district (Kyzylalmasay, Arabulak) are close in composition. They are characterized by development of intermetallides, sulfides, sulfosalts, and selenides of Au-Ag and occasionally Au-Sb associations. Fineness of gold decreases from early to late geochemical associations, whereas the size of gold grains increases in the same direction from nanogold to visible gold. The studies at the micro- and nanolevel make it possible to establish the attributes of specific gold mineralization, to substantiate prospecting guides, and to estimate the erosion level and resource potential of hidden ore objects. The greater and more diverse a set of micro- and nanominerals, the larger a gold deposit is.  相似文献   

16.
Chemical composition and mode of occurrences of (Au, Ag)Te2 minerals such as calaverite (AuTe2), sylvanite (AuAgTe4) and krennerite ((Au, Ag)Te2) in epithermal gold telluride ores from Suzaki, Kawazu and Teine are examined. In the ores from Suzaki, (Au, Ag)Te2 minerals occur in microbands of tellurides and fine quartz. The minerals in telluride bands change from krennerite, via calaverite‐native tellurium, to sylvanite, in the order of crystallization. A sample from Kawazu contains sylvanite and native tellurium with stutzite, hessite and tetradymite in the coarser gray quartz part. The Teine sample also contains sylvanite and native tellurium with barite and quartz. The peak patterns of XRD of calaverite, krennerite and sylvanite from Suzaki are almost identical to that of JCPDS 43–1472, JCPDS 8–20 and JCPDS 9–477, respectively. The Te, Au, Cu, and Ag contents of calaverite from Suzaki range from 56.4 to 57.9 wt.%, from 41.6 to 42.6 wt.%, from 0.28 to 0.45 wt.% and from 0.14 to 0.31 wt.%, respectively, corresponding to the formula Au0.97Ag0.01Cu0.02Te2. The Te, Au, Ag, and Cu contents of krennerite from Suzaki range from 59.6 to 61.4 wt.%, from 31.3 to 33.6 wt.%, from 4.91 to 6.13 wt.% and from 0.66 to 0.80 wt.%, respectively, corresponding to the formula Au0.71Ag0.22Cu0.05Te2 with Au and Ag ranging from 0.68 to 0.74 and from 0.20 to 0.25, respectively. The Te, Au, Ag, and Cu contents of sylvanite from Suzaki range from 61.5 to 63.4 wt.%, from 24.1 to 27.4 wt.%, from 10.0 to 12.5 wt.% and from 0.00 to 0.12 wt.%, respectively. The Te, Au, Ag, and Cu contents of sylvanite from Kawazu range from 62.7 to 63.3 wt.%, from 23.5 to 24.1 wt.%, from 12.0 to 12.5 wt.% and from 0.09 to 0.16 wt.%, respectively. The Te, Au, Ag, Cu and Fe contents of sylvanite from Teine range from 61.8 to 63.5 wt.%, from 23.6 to 24.7 wt.%, from 11.9 to 13.3 wt.%, from 0.01 to 1.65 wt.% and from 0.00 to 0.02 wt.%, respectively. The average formulae of sylvanite from Suzaki, Kawazu, and Teine are expressed as Au1.06Ag0.94Cu0.02Te4, Au1.00Ag0.95Cu0.02Te4 and Au1.01Ag0.95Cu0.06Te4, respectively. Judging from the mineral assemblages of these ores and other localities, Au–Te mineralization in the Japanese Islands can be divided into four types: native gold–calaverite at Date and Agawa, krennerite(?native tellurium) at Osore‐zan and Mutsu, sylvanite–native tellurium–hessite at Teine, Kawazu, Kobetsuzawa, and Kato, and polyminerallic assemblages at Suzaki and Kushikino. The pH–Eh diagram of aqueous tellurium species and tellurium minerals at 250°C indicates that (Au, Ag)Te2 minerals in epithermal gold telluride mineralization would have been formed under middle to low Eh and acidic (to intermediate) pH conditions. It is possible that dilute tellurium‐containing fluid would scavenge dilute gold.  相似文献   

17.
赵善仁  吴悦斌 《现代地质》1996,10(4):478-484
五台山—恒山绿岩带Ａｕ、Ａｇ、Ｃｕ矿床可分为二大类型：（１）再生型金银铜矿，产在包括岩浆岩在内的各类岩石断裂构造中，与岩浆期后热液有关；（２）变生型金银铜矿，产于各类变质岩中，具有层控特征（即绿岩型金矿）。在地球化学特征上，再生型矿床与变生型矿床相比，矿体及围岩中Ｍｏ、Ａｇ、Ｐｂ、Ｚｎ、Ｃｄ等成矿及伴生元素明显富集；Ｋ２Ｏ、Ｒｂ、Ｓｒ、Ｂａ、Ｔｈ、Ｕ也明显富集，是后期岩浆热液作用的结果；Ｈｇ、Ｆ的明显富集则与后期构造活动有关；Ｚｎ／Ｃｄ比值较低，说明受到后期岩浆侵入影响；Ｔｈ／Ｕ比值低，可能指示富钙的酸性岩环境。再生型Ａｕ矿化的元素组合为Ｃｄ、Ａｓ、Ｎｉ、Ａｇ、Ｓｂ、Ａｕ、Ｈｇ（Ｂｉ），再生型Ａｇ矿化的元素组合为Ａｓ、Ｓｂ、Ａｇ、Ｃｄ、Ｃｕ、Ｎｉ（Ｍｏ、Ｐｂ、Ｚｎ、Ｂｉ），变生型Ａｕ矿化的元素组合较简单，只为Ａｕ、Ｈｇ、Ａｓ或Ａｕ、Ｃｕ。上述地球化学特征不仅可以有效地区分矿化类型，而且可以作为地球化学找矿和评价的指标  相似文献   

18.
三家金矿发现Hg—Au—Ag矿物—α—汞金银矿   总被引：1，自引：0，他引：1  
a-汞金银矿是1986年笔者在河北省青龙县三家金矿某富矿带采集的金矿石标本中发现的,见于矿石光片及人工重砂中。经电子探针分析,平均含Ag 41.53%,Au 22.34%,Hg 36.09%,简化化学式为:(Ag,Au)3Hg。其x射线粉晶数据为:2.382(9) (111),2.060(6)(200),1.461(7)(220),1.245(10)(311),1.194(5)(222),与1929年Pabst等人合成的a汞金矿(含Au 82.75%)可以比较,属等轴晶系。笔者确定它为Hg、Au、Ag金属互化物,且是Hg-Au-Ag系列矿物的新变种。  相似文献   

19.
‘Invisible gold’ in bismuth chalcogenides   总被引：1，自引：0，他引：1  
Gold concentrations have been determined by LA-ICPMS in bismuth chalcogenides (tellurides and sulfosalts, minerals with modular structures; chalcogen X = Te, Se, and S) from 27 occurrences. Deposit types include epithermal, skarn, intrusion-related and orogenic gold. The samples comprised minerals of the tetradymite group, aleksite series, bismuth sulfosalts (cosalite, lillianite, hodrushite, bismuthinite, and aikinite), and accompanying altaite. Gold concentrations in phases of the tetradymite group range from <0.1 to 2527 ppm. Phases in which Bi > X tend to contain lower gold concentrations than Bi2X3 minerals (tellurobismuthite and tetradymite). Cosalite and lillianite contain Au concentrations ranging up to 574 and 3115 ppm, respectively. Bismuthinite derivatives have lower Au concentrations: <2 ppm in bismuthinite and up to 542 ppm in aikinite. In our samples, Au concentrations in altaite range from <0.2 to 1662 ppm.Smoother parts of the LA-ICPMS profiles suggest lattice-bound gold, whereas irregularities on the profiles are best explained by the presence of gold particles (?1 μm in diameter). Plotting Au vs. Ag for the entire dataset gives a wedge-shaped distribution, suggesting that Ag underpins Au uptake in both bismuth tellurides and sulfosalts. In the tellurides, correlation trends suggest statistical substitution of Ag(Au), together with Pb, into the octahedral site in the layers. In sulfosalts, Au follows coupled substitutions in which M1+ (Ag, Cu) enters the structure. In tellurides, the presence of van der Waals gaps at chalcogen-chalcogen contacts provides for p-type semi-conductive properties critical for gold scavenging from fluids. Such weak bonds may also act as sites for nucleation of Au (nano)particles. In sulfosalts, contacts between different species that replace one another are also highly predictable to act as traps for (nano)particulate gold.Invisible gold in Bi-chalcogenides is useful to (i) identify trends of orefield zonation, (ii) discriminate between ‘melt’ and ‘fluid-driven’ scavenging, and (iii) interpret replacement and remobilisation processes. Bismuth chalcogenides have the potential to be significant Au carriers in sulfide-poor Au systems, e.g., intrusion-related gold, with impact on the overall Au budget if mean Au concentrations are high enough and the minerals are sufficiently abundant.  相似文献   

20.
基于GIS空间分析技术,对云南澜沧江中南段多金属矿床的赋矿地层时间谱系、容矿构造空间谱系和矿床成因谱系进行了较系统的分析.研究表明,下-中元古界、三叠系、泥盆系、二叠系是本区最重要的赋矿层位,有两个聚矿期和多个时代地层含矿的特点,不同时代地层的含矿性具有多样性和专属型特征,元古宙火山沉积为主的建造是铁-铜、钨-锡矿为主的赋矿层位,晚古生代-中生代早期是沉积、裂谷火山活动强烈时期,金、铜、铅、锌、银、汞、锑、钨、锡多金属矿床高度聚集.自东向西为中生代坳陷区金、铜、镍成矿带,思茅-龙洞河晚古生代-三叠纪沉积盆地铜、铅、锌、银成矿带,岩浆弧地块钨、锡、铅-锌、铁成矿带,浅变质岩基底铅-锌-银、铁成矿带,被动边缘活动带金、铅-锌-银、锡成矿区和保山-镇康微地块铅-锌、铜、铁、汞成矿带,构成了容矿构造空间谱系.全区多金属矿床有沉积、沉积改造、岩浆-变质热液、火山沉积-火山热液四大成矿谱系,14种成矿类型,铜多金属、铅-锌-银、锡-钨矿床是研究区最具找矿前景的优势矿种.  相似文献   

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