Stratigraphy and base metal mineralization in the Otavi Mountain Land, Northern Namibia—a review and regional interpretation

Sediment-hosted base metal sulfide deposits in the Otavi Mountain Land occur in most stratigraphic units of the Neoproterozoic Damara Supergroup, including the basal Nosib Group, the middle Otavi Group and the uppermost Mulden Group. Deposits like Tsumeb (Pb–Cu–Zn–Ge), Kombat (Cu–Pb–Zn), Berg Aukas (Zn–Pb–V), Abenab West (Pb–Zn–V) all occur in Otavi Group dolostones, whereas siliciclastic and metavolcanic rocks host Cu–(Ag) or Cu–(Au) mineralization, respectively. The Tsumeb deposit appears to have been concentrated after the peak of the Damara orogeny at around 530 Ma as indicated by radiometric age data.Volcanic hosted Cu–(Au) deposits (Neuwerk and Askevold) in the Askevold Formation may be related to ore forming processes during continental rifting around 746 Ma. The timing of carbonate-hosted Pb–Zn deposits in the Abenab Subgroup at Berg Aukas and Abenab is not well constrained, but the stable (S, O, C) and Pb isotope as well as the ore fluid characteristics are similar to the Tsumeb-type ores. Regional scale ore fluid migration typical of MVT deposits is indicated by the presence of Pb–Zn occurrences over 2500 km² within stratabound breccias of the Elandshoek Formation. Mulden Group siliciclastic rocks host the relatively young stratiform Cu–(Ag) Tschudi resource, which is comparable to Copperbelt-type sulfide ores.     

Geochronological framework and Pb, Sr isotope geochemistry of the Qingchengzi Pb–Zn–Ag–Au orefield, Northeastern China

The Qingchengzi orefield in northeastern China, is a concentration of several Pb–Zn, Ag, and Au ore deposits. A combination of geochronological and Pb, Sr isotopic investigations was conducted. Zircon SHRIMP U–Pb ages of 225.3 ± 1.8 Ma and 184.5 ± 1.6 Ma were obtained for the Xinling and Yaojiagou granites, respectively. By step-dissolution Rb–Sr dating, ages of 221 ± 12 Ma and 138.7 ± 4.1 Ma were obtained for the sphalerite of the Zhenzigou Zn–Pb deposit and pyrargyrite of the Ag ore in the Gaojiabaozi Ag deposit, respectively. Pb isotopic ratios of the Ag ore at Gaojiabaozi (²⁰⁶Pb/²⁰⁴Pb = 18.38 to 18.53) are higher than those of the Pb–Zn ores (²⁰⁶Pb/²⁰⁴Pb = 17.66 to 17.96; Chen et al. [Chen, J.F., Yu, G., Xue, C.J., Qian, H., He, J.F., Xing, Z., Zhang, X., 2005. Pb isotope geochemistry of lead, zinc, gold and silver deposit clustered region, Liaodong rift zone, northeastern China. Science in China Series D 48, 467–476.]). Triassic granites show low Pb isotopic ratios (²⁰⁶Pb/²⁰⁴Pb = 17.12 to 17.41, ²⁰⁷Pb/²⁰⁴Pb = 15.47 to 15.54, ²⁰⁸Pb/²⁰⁴Pb = 37.51 to 37.89) and metamorphic rocks of the Liaohe Group have high ratios (²⁰⁶Pb/²⁰⁴Pb = 18.20 to 24.28 and 18.32 to 20.06, ²⁰⁷Pb/²⁰⁴Pb = 15.69 to 16.44 and 15.66 to 15.98, ²⁰⁸Pb/²⁰⁴Pb = 37.29 to 38.61 and 38.69 to 40.00 for the marble of the Dashiqiao Formation and schist of the Gaixian Formation, respectively).Magmatic activities at Qingchengzi and in adjacent regions took place in three stages, and each contained several magmatic pulses: ca. 220 to 225 Ma and 211 to 216 Ma in the Triassic; 179 to 185 Ma, 163 to 168 Ma, 155 Ma and 149 Ma in the Jurassic, as well as ca. 140 to 130 Ma in the Early Cretaceous. The Triassic magmatism was part of the Triassic magmatic belt along the northern margin of the North China Craton produced in a post-collisional extensional setting, and granites in it formed by crustal melting induced by mantle magma. The Jurassic and Early Cretaceous magmatism was related to the lithospheric delamination in eastern China. The Triassic is the most important metallogenic stage at Qingchengzi. The Pb–Zn deposits, the Pb–Zn–Ag ore at Gaojiabaozi, and the gold deposits were all formed in this stage. They are temporally and spatially associated with the Triassic magmatic activity. Mineralization is very weak in the Jurassic. Ag ore at Gaojiabaozi was formed in the Early Cretaceous, which is suggested by the young Rb–Sr isochron age, field relations, and significantly different Pb isotopic ratios between the Pb–Zn–Ag and Ag ores. Pb isotopic compositions of the Pb–Zn ores suggest binary mixing for the source of the deposits. The magmatic end-member is the Triassic granites and the other metamorphic rocks of the Liaohe Group. Slightly different proportions of the two end-members, or an involvement of materials from hidden Cretaceous granites with slightly different Pb isotopic ratios, is postulated to interpret the difference of Pb isotopic compositions between the Pb–Zn–(Ag) and Ag ores. Sr isotopic ratios support this conclusion. At the western part of the Qingchengzi orefield, hydrothermal fluid driven by the heat provided by the now exposed Triassic granites deposited ore-forming materials in the low and middle horizons of the marbles of the Dashiqiao Formation near the intrusions to form mesothermal Zn–Pb deposits. In the eastern part, hydrothermal fluids associated with deep, hidden Triassic intrusions moved upward along a regional fault over a long distance and then deposited the ore-forming materials to form epithermal Au and Pb–Zn–Ag ores. Young magmatic activities are all represented by dykes across the entire orefield, suggesting that the corresponding main intrusion bodies are situated in the deep part of the crust. Among these, only intrusions with age of ca. 140 Ma might have released sufficient amounts of fluid to be responsible for the formation of the Ag ore at Gaojiabaozi.Our age results support previous conclusions that sphalerite can provide a reliable Rb–Sr age as long as the fluid inclusion phase is effectively separated from the “sulfide” phase. Our work suggests that the separation can be achieved by a step-resolution technique. Moreover, we suggest that pyrargyrite is a promising mineral for Rb–Sr isochron dating.     

Environmental impact of the former Pb–Zn mining and smelting in East Belgium

In the mining district of Plombières-La Calamine (East Belgium), extensive Pb–Zn mining activities resulted in an important contamination of overbank sediments along the Geul river. Moreover, a huge amount of heavy metals is stored in a dredged mine pond tailing, which is located along the river. In the dredged mine pond tailing sediments, Pb–Zn minerals control the solubility of Zn, Pb and Cd. Although Pb, Zn and Cd display a lower solubility in overbank sediments compared to the mine tailing pond sediments, elevated concentrations of Pb, Zn and Cd are still found in the porewater of the overbank sediments. The considerable ‘actual’ and ‘potential’ mobility of Zn, Pb and Cd indicates that the mine pond tailing sediments and the overbank sediments downstream from the mine pond tailing represent a considerable threat for the environment. Besides the chemical remobilisation of metals from the sediments, the erosion of overbank sediments and the reworking of riverbed sediments act as a secondary source of pollution.     

Brine pool deposition for the Zn–Pb–Cu massive sulphide deposits of the Bathurst mining camp, New Brunswick, Canada. I. Comparisons with the Iberian pyrite belt

The Ordovician Zn–Pb–Cu massive sulphide ore deposits of the Bathurst mining camp share many features with those of the Devonian/Carboniferous Iberian pyrite belt, particularly the tendency to large size (tonnage and metal content); shape, as far as can be determined after allowing for deformation; metal content, particularly Fe/Cu, Pb/Zn and Sn; mineral assemblages (pyrite + arsenopyrite ± pyrrhotite and lack or rarity of sulphates); sulphide textures (particularly framboidal pyrite); lack of chimney structures and rubble mounds; irregular metal or mineral zoning; and the low degree of zone refining compared to Hokuroku ores. The major differences between the provinces are the lack of vent complexes and the presence of Sn–Cu ores in the Iberian pyrite belt. There are also similarities in the geological setting of the two camps: both lie within continental terranes undergoing arc-continent and continent–continent collision, and in each case massive sulphide mineralisation followed ophiolite obduction; the ore deposits are associated with bimodal volcanic rocks derived from MORB and continental crust and marine shales; and mineralisation was locally accompanied or followed by deposition of iron formations.Fluid inclusion data from veins in stockworks from at least six of the Iberian massive sulphide deposits point to sulphide deposition having taken place in basins containing mostly spent saline, ore-forming fluids (brine pools), and it is suggested that most of the major features of the Bathurst deposits can be explained by similar processes. The proposed model is largely independent of ocean sulphate and O₂ content, whereas low values of each are requisites for the current, spreading-plume model of sulphide deposition in the Bathurst camp.     

Geological features and origin of the Huize carbonate-hosted Zn–Pb–(Ag) District, Yunnan, South China

The Huize Zn–Pb–(Ag) district, in the Sichuan–Yunnan–Guizhou Zn–Pb–(Ag) metallogenic region, contains significant high-grade, Zn–Pb–(Ag) deposits. The total metal reserve of Zn and Pb exceeds 5 Mt. The district has the following geological characteristics: (1) high ore grade (Zn + Pb ≥ 25 wt.%); (2) enrichment in Ag and a range of other trace elements (Ge, In, Ga, Cd, and Tl), with galena, sphalerite, and pyrite being the major carriers of Ag, Ge, Cd and Tl; (3) ore distribution controlled by both structural and lithological features; (4) simple and limited wall-rock alteration; (5) mineral zonation within the orebodies; and (6) the presence of evaporite layers in the ore-hosting wall rocks of the Early Carboniferous Baizuo Formation and the underlying basement.Fluid-inclusion and isotope geochemical data indicate that the ore fluid has homogenisation temperatures of 165–220 °C, and salinities of 6.6–12 wt.% NaCl equiv., and that the ore-forming fluids and metals were predominantly derived from the Kunyang Group basement rocks and the evaporite-bearing rocks of the cover strata. Ores were deposited along favourable, specific ore-controlling structures. The new laboratory and field studies indicate that the Huize Zn–Pb–(Ag) district is not a carbonate-replacement deposit containing massive sulphides, but rather the deposits can be designated as deformed, carbonate-hosted, MVT-type deposits. Detailed study of the deposits has provided new clues to the localisation of concealed orebodies in the Huize Zn–Pb–(Ag) district and of the potential for similar carbonate-hosted sulphide deposits elsewhere in NE Yunnan Province, as well as the Sichuan–Yunnan–Guizhou Zn–Pb–(Ag) metallogenic region.     

2: Hydrothermal ore deposits related to post-orogenic extensional magmatism and core complex formation: The Rhodope Massif of Bulgaria and Greece

The Rhodope Massif in southern Bulgaria and northern Greece hosts a range of Pb–Zn–Ag, Cu–Mo and Au–Ag deposits in high-grade metamorphic, continental sedimentary and igneous rocks. Following a protracted thrusting history as part of the Alpine–Himalayan collision, major late orogenic extension led to the formation of metamorphic core complexes, block faulting, sedimentary basin formation, acid to basic magmatism and hydrothermal activity within a relatively short period of time during the Early Tertiary. Large vein and carbonate replacement Pb–Zn deposits hosted by high-grade metamorphic rocks in the Central Rhodopean Dome (e.g., the Madan ore field) are spatially associated with low-angle detachment faults as well as local silicic dyke swarms and/or ignimbrites. Ore formation is essentially synchronous with post-extensional dome uplift and magmatism, which has a dominant crustal magma component according to Pb and Sr isotope data. Intermediate- and high-sulphidation Pb–Zn–Ag–Au deposits and minor porphyry Cu–Mo mineralization in the Eastern Rhodopes are predominantly hosted by veins in shoshonitic to high-K calc-alkaline volcanic rocks of closely similar age. Base-metal-poor, high-grade gold deposits of low sulphidation character occurring in continental sedimentary rocks of synextensional basins (e.g., Ada Tepe) show a close spatial and temporal relation to detachment faulting prior and during metamorphic core complex formation. Their formation predates local magmatism but may involve fluids from deep mantle magmas.The change in geochemical signatures of Palaeogene magmatic rocks, from predominantly silicic types in the Central Rhodopes to strongly fractionated shoshonitic (Bulgaria) to calc-alkaline and high-K calc-alkaline (Greece) magmas in the Eastern Rhodopes, coincides with the enrichment in Cu and Au relative to Pb and Zn of the associated ore deposits. This trend also correlates with a decrease in the radiogenic Pb and Sr isotope components of the magmatic rocks from west to east, reflecting a reduced crustal contamination of mantle magmas, which in turn correlates with a decreasing crustal thickness that can be observed today. Hydrogen and oxygen isotopic compositions of the related hydrothermal systems show a concomitant increase of magmatic relative to meteoric fluids, from the Pb–Zn–Ag deposits of the Central Rhodopes to the magmatic rock-hosted polymetallic gold deposits of the Eastern Rhodopes.     

Sanjiang Tethyan metallogenesis in S.W. China: Tectonic setting, metallogenic epochs and deposit types

Tectonically, the Sanjiang Tethyan Metallogenic Domain (STMD) is located within the eastern Himalayan–Tibetan Orogen in the Sanjiang Tethys, southwestern China. Although this metallogenic domain was initiated in the Early Palaeozoic, extensive metallogenesis occurred in the Late Palaeozoic, Late Triassic and Himalayan (Tertiary) epochs. Corresponding tectonic settings and environments in the domain are: an arc-basin system related to the subduction of the Palaeo-Tethyan oceanic slabs; a post-collision crustal extension setting caused by the lithospheric delamination or slab breakoff underneath the Sanjiang Tethys during the Late Triassic; large-scale strike-slip faulting and thrusting systems due to the Indo-Asian continent collision since the Palaeocene. In this metallogenic domain important gold, copper, base metals, rare metals and tin ore belts, incorporating a large number of giant deposits, were developed. The main types of deposits include: (1) porphyry copper deposits, controlled by a large-scale strike-slip fault system, (2) VHMS deposits, mainly occurring in intra-arc rift basins and post-collision crustal extensional basins, (3) shear-zone type gold deposits in the ophiolitic mélange zone along the thrusting–shearing system, (4) hydrothermal silver-polymetallic deposits in the Triassic intra-continental rift basins and Tertiary strike-slip pull-apart basins, and (5) Himalayan granite-related greisen-type tin and rare-metallic deposits. Within the metallogenic epochs of the Late Palaeozoic to Cenozoic, the styles and types of the ore deposits changed from VHMS types in the Late Palaeozoic through exhalative-sedimentary type deposits in the Late Triassic, to porphyry-type copper deposits, shear-zone type gold deposits, hydrothermal vein-type silver-polymetallic deposits, greisen-type tin and rare-metal deposits in the Cenozoic. Correspondingly, ore-forming metals also changed from a Pb–Zn–Cu–Ag association through Ag–Cu–Pb–Zn, Fe–Ag–Pb and Ag–Au–Hg associations, to Ag–Cu–Pb–Zn, Cu–Mo, Au, Sn, and Li–Rb–Cs–Nb–Zr–Hf–Y–Ce–Sc associations.     

Laser microprobe sulphur isotope analysis of arsenopyrite: experimental calibration and application to the Boliden Au–Cu–As massive sulphide deposit

Metamorphic remobilization of arsenopyrite-rich ores is a globally important process which can lead to significant concentrations of gold. In order to understand this and related processes, relations of sulphur isotopes can give a number of important clues. To resolve such relations in detail, we have successfully calibrated and applied a laser combustion system for in situ analysis of sulphur isotopic compositions of arsenopyrite. Experimental calibration of the laser fractionation factor (+0.4‰) was obtained by using compositionally and isotopically homogeneous natural samples from ore deposits at Boliden (Sweden) and Freiberg (Germany); subsequent to detailed microscopic study, the S isotope ratios of these samples were measured by conventional and laser combustion techniques.The present application to different types of arsenopyrite in the Palaeoproterozoic metamorphosed VHMS ores of the Boliden Au–Cu–As deposit, Skellefte district, northern Sweden, shows that the sulphur isotope composition of arsenopyrite is essentially unmodified during medium-grade metamorphic recrystallization and remobilization. Here, massive arsenopyrite ore is crosscut by later veins that carry a complex quartz–sulphosalt–sulphide assemblage. The latter ore type is markedly Au-rich compared to the host ore, and thus of significant economic interest. We find that both ore types exhibit very similar sulphur isotope compositions, ca. +2‰ to +3‰ (V-CDT), which is similar to most massive sulphide deposits in the Skellefte district. Thus, the crosscutting Au-rich vein ore has inherited the sulphur isotope composition from sulphur liberated by metamorphic reactions affecting the massive ore, and most likely also inherited the Au through this mechanism. The latter finding clearly has important implications both for the general discussion on, and the prospecting for, similar high-grade Au ores in this world-class mining region.     

Alluvial records of medieval and prehistoric tin mining on Dartmoor,southwest England

The role of tin mining in the society of prehistoric Dartmoor and its impact on the local landscape have long been discussed despite equivocal evidence for prehistoric mine sites. A fluvial geomorphological approach, using floodplain stratigraphy, combined with sediment geochemistry and mineralogy, was employed to identify prehistoric tin mining at the catchment scale. Waste sediment, released during hydraulic mining of alluvial tin deposits, caused downstream floodplain aggradation of sands with a diagnostic signature of elevated Sn concentration within the silt fraction. At a palaeochannel site in the Erme Valley, sediment aggradation buried datable peat deposits. A period of aggradation postdating cal. A.D. 1288–1389 is consistent with the 13th century peak in tin production identified in the documentary record. An earlier phase of aggradation, however, occurred between the 4th and 7th centuries A.D., providing evidence of late Roman or early Post Roman tin mining activity on Dartmoor. © 2004 Wiley Periodicals, Inc.     

Halogen elements as indicator of deep-seated orebodies in the Chadong As–Ag–Au deposit, western Guangdong, China

Halogen elements play an important role in the metallogenesis of metallic ore deposits and are involved in the whole process of remobilization, transport and precipitation of metallic elements. However, with the exception of fluorine, which, as a component of fluorite and mica minerals, can be occasionally concentrated in ores, Cl, Br and I are hard to enrich in the ores. Investigations have found that the halogen elements tend to diffuse toward country rocks with the development of hydrothermal alteration in the process of their involvement in metallogenesis, especially during the post-ore stage when extensive halogen diffusion halos over orebodies would be formed. Such halogen element diffusion halos over the Chadong As–Ag–Au deposit extend as widely as 200 m. The largest diffusion extent is for I and the diffusion halos of Br are most noticeable 50–130 m away from the orebodies. In areas of ore exposure and the strongly altered zone, the Cl, Br and I contents are close to those of the strata with a V-shaped distribution pattern in the periphery of the mining district. Comparatively speaking, in going away from the altered zone, the major metallic elements Au and Ag in the deposit tend to decrease suddenly to their normal contents in the strata. This variation feature of halogen elements can be used as geochemical indicators for exploring concealed orebodies at depth. In the Chadong ore deposit, halogen element anomalies can be used to predict concealed orebodies at the depth range of 0–200 m.     

青海德尔尼铜(锌钴)矿床Re-Os年龄及地质意义

东昆仑德尔尼大型铜(锌钴)矿是赋存在蛇绿岩中的块状硫化物矿床,8件块状硫化物矿石的Re-Os同位素等时线年龄为(295.5±7.2) Ma,略小于矿区玄武质熔岩的锆石U-Pb平均年龄(308.2±4.9) Ma,矿床形成于晚石炭世-早二叠世,属于阿尼玛卿洋盆扩张期。成矿时代早于矿区北部印支期花岗岩,证明德尔尼矿床的成因与印支期花岗岩无直接关系。矿石组构、矿物组合和岩石地球化学研究指示,矿床为海底喷流沉积-热液叠加成矿,具有类似于塞浦路斯型块状硫化物矿床的构造背景和矿物组合特征。矿区及外围填图发现,德尔尼铜矿体主要产出在角砾状蛇纹岩中,部分位于蛇纹岩与含碳铁硅质岩之间,这种特殊的赋矿层位可能与晚古生代特提斯洋的快速扩张、岩浆补给少、变质橄榄岩迅速抬升有关。     

皖南上震旦统蓝田组中银铅锌等多金属矿床成因探讨

皖南地区上震旦统蓝田组，是银铅锌等多金属矿床的重要赋矿层位，区域地质，矿床地质和地球化学特征研究表明，银铅锌等多金属矿床是由于热水沉积作用而形成，热水沉积作用受断裂控制明显，主要呈带状沿着祁门－三阳坑一万家桥深断裂NE方向展布，热水学沉积形成了银铅锌等多金属矿床，铁锰矿床以及蓝田组底部数千平方千米含锰碳酸盐岩，这一认识不仅为皖南地区矿床的成因给予了新的解释，也为今后该区矿产资源的勘察工作提供了新的思路。     

Zn–Pb–Cu volcanic-hosted massive sulphide deposits: criteria for distinguishing brine pool-type from black smoker-type sulphide deposition

Eight Zn–Pb–Cu massive sulphide deposits that appear to have formed on the sea floor (seven in Spain, one in Tasmania) are believed to have been precipitated in brine pools, based on the salinities and temperatures of fluid inclusions in underlying stockworks. Comparing the geological features of these deposits with those of the Zn–Pb–Cu massive sulphide ores of the Hokuroku Basin, Japan, which have formed as mounds from buoyant fluids of low salinity, shows that brine pool deposits have: (1) potentially very large size and tonnage, and high aspect ratio, (2) higher Zn/Cu and Fe/Cu values, (3) no evidence of chimneys, (4) relatively abundant framboidal pyrite and primary mineral banding, (5) reduced mineral assemblages (pyrite-arsenopyrite/pyrrhotite), and minor or rare barite in the massive sulphide, (6) associated stratiform and/or vein carbonates, (7) relatively unimportant zone refining, (8) lack of vertical variation in sphalerite and sulphur isotopic compositions, and (9) evidence of local bacterial sulphate reduction. Application of these criteria to the Rosebery deposit in Tasmania, for which there are no fluid inclusion data, leads to the conclusion that the southern section was deposited as separate lenses in a brine-filled basin or basins. Other potential candidates include Brunswick no. 12 and Heath Steele (Canada), Woodlawn and Captains Flat (New South Wales), Hercules and Que River (Tasmania), and Tharsis and the orebodies at Aljustrel (Spain and Portugal). Recently published fluid inclusion data for Gacun (China) and Mount Chalmers (Queensland) suggest that not all ores deposited from highly saline fluids have reduced mineral assemblages.     

Modeling of fluid pressure evolution related to sediment loading and thrust faulting in the Lanping basin: Implications for the formation of the Jinding Zn–Pb deposit, Yunnan, China

The Jinding Zn–Pb deposit occurs in Cretaceous and Paleocene siliciclastic rocks (mainly sandstones) in the Meso-Cenozoic Lanping basin, western Yunnan, China. With a reserve of approximately 200 Mt of ore containing 6.1% Zn and 1.3% Pb, Jinding is the largest sandstone-hosted Zn–Pb deposit in the world. Most previous studies assumed that the mineralizing fluids were derived from within the basin (including meteoric recharge), and the fluid flow was driven by topographic relief under a hydrostatic regime. In contrast, we propose that the mineralizing system was strongly overpressured based on observations of hydraulic fractures and fluid inclusion data. Numerical modeling results indicate that the overpressures could not have been produced by normal sediment compaction. Thrust faulting and input of mantle-derived fluids are likely responsible for the building-up of the high overpressures. The special hydrodynamic regime and potential contribution of mantle-derived fluids to the mineralizing system distinguish Jinding from other known sedimentary basin-related Pb–Zn deposits.     

Genetic significance of fluid inclusions in the CSA Cu–Pb–Zn deposit, Cobar, Australia

CSA mine exploits a ‘Cobar-type’ Cu–Pb–Zn±Au±Ag deposit within a cleaved and metamorphosed portion of the Cobar Supergroup, central New South Wales. The deposit comprises systems of ‘lenses’ that encompass veins, disseminations and semi-massive to massive Cu–Pb–Zn ores. The systems and contained lenses truncate bedding, are approximately coplanar with regional cleavage and similarly oriented shear zones and plunge parallel to the elongation lineation. Systems have extreme vertical continuity (>1000 m), short strike length (400 m) and narrow width (100 m), exhibit vertical and lateral ore-type variation and have alteration haloes. Models of ore formation include classical hydrothermalism, structurally controlled remobilisation and polymodal concepts; syntectonic emplacement now holds sway.Fluid inclusions were examined from quartz±sulphide veins adjacent to now-extracted ore, from coexisting quartz–sulphide within ore, and from vughs in barren quartz veins. Lack of early primary inclusions precluded direct determination of fluids associated with D₂–D₃ ore and vein emplacement. Similarly, decrepitation (by near-isobaric heating) of the two oldest secondary populations precluded direct determination of fluid phases immediately following D₂–D₃ ore and vein emplacement. Post-decrepitation outflow (late D₃ to early post-D₃) is recorded by monophase CH₄ inclusions. Entrained outflow of deeply circulated meteoric fluid modified the CH₄ system; modification is recorded by H₂O+CH₄ and H₂O+(trace CH₄) secondary populations and by an H₂O+(trace CH₄) primary population. The contractional tectonics (D₂–D₃) of ore emplacement was superseded by relaxational tectonics (D_4P) that facilitated meteoric water penetration and return flow.Under D₂ prograde metamorphism, entrapment temperatures (Tt) and pressures (Pt) for pre-decrepitation secondary inclusions are estimated as Tt300–330 °C and Pt1.5–2 kbar≈Plith (the lithostatic pressure). Decrepitation accompanied peak metamorphism (T350–380 °C) in mid- to late-D₃, while in late-D₃ to early post-D₃, essentially monophase CH₄ secondary inclusions were entrapped at Tt350 °C and Pt=1.5–2 kbar≈Plith. Subsequently, abundant CH₄ and entrained meteoric water were entrapped as H₂O+CH₄ secondaries under slowly decreasing temperature (Tt330–350 °C) and constant pressure (Pt1.5–2 kbar). Finally, with increasingly dominant meteoric outflow, H₂O+(trace CH₄) populations record decreasing temperatures (Tt>300 to <350 down to 275–300 °C) at pressures of Phydrostatic<Pt (1 kbar) <Plith (1.5 kbar).The populations of inclusions provide insight into fluid types, flow regimes and P–T conditions during parts of the deposit's evolution. They indirectly support the role of basin-derived CH₄ fluids in ore formation, but provide no insight into a basement-sourced ore-forming fluid. They fully support post-ore involvement of meteoric water. The poorly constrained entrapment history is believed to span 10 Ma from 395 to 385 Ma.     

Refractory- and metallurgical-type chromite ores,Zambales ophiolite,Luzon, Philippines

The Zambales ophiolite is the major source of chromite ore in the Philippines. The chromitites are concordant cumulates and are associated with distinct chromitite-bearing sequences within the mantle peridotites. Refractory and metallurgical chromite deposits are spatially separated and related to different lithologic associations, which crystallized from different parental magmas. — Refractory chromite ores (30–44 wt% Cr₂O₃; 20–30 wt% Al₂O₃) are linked with the peridotite-troctolite-olivine gabbro lineage. Two main types were found: (1) Al-rich refractory ores associated with harzburgites and feldspathic periodotites and (2) more Cr-rich varieties associated with lherzolites. — Metallurgical chromite ores (45–53 wt% Cr₂O₃; 12–18 wt% Al₂O₃) are linked with the peridotite-pyroxenite-norite lineage. Two main types were also found: (1) Cr-rich metallurgical ores associated with orthopyroxenites and (2) more Al-rich varieties related to clinopyroxenites. — The chemical composition of chromite within the deposits varies depending on the chromite/silicate ratios of the ore types and grades continuously into accessory chrome spinels in the wall-rock peridotites. — The geochemistry of accessory chrome spinels in various peridotites and mafic cumulates depends on the mineralogical composition and the stratigraphic position of their host rocks.New address: BEB Erdgas und Erdöl GmbH, Riethorst 12, D-3000 Hannover 51The terms chrome-spinels and chromite are used as follows: 1. Chrome-spinel is only used for those occuring as accessory minerals in various ultramafic and mafic rocks (= accessory chrome-spinels). Their chemical composition has been determined only by microprobe analysis. — 2. Chromite is used for ore and ore deposits (=chromitites); the chemical composition has been determined by wet chemistry (AAS) or by microprobe analysis     

Zn/Cd ratios in calcsilicate-hosted sphalerite ores at Tumurtijn-ovoo, Mongolia

As other calcsilicate-hosted ore deposits the Tumurtijn-ovoo Fe–Mn–Zn deposit is subdued to the question how the ore elements took place, whether linked to epigenetic silicification of a limestone host or bound to syngenetic precipitation during the deposition of a calcareous-siliceous sediment. The comparison of high Zn/Cd ratios of ores from Tumurtijn-ovoo ranging from 514 to 724 with those of other ore deposits relates Tumurtijn-ovoo to the group of submarine hydrothermal deposits which got their ore elements from basaltic source rocks by subseafloor leaching. Hence, respecting geological and textural features of the ores, a synsedimentary precipitation of zinc and cadmium in a volcano-sedimentary environment is suggested for Tumurtijn-ovoo. A group of low Zn/Cd ratios (274–297) is correlated with processes of mobilization and redeposition of sphalerite.     

Lithogeochemical halos and geochemical vectors to stratiform sediment hosted Zn–Pb–Ag deposits, 1. Lady Loretta Deposit, Queensland

Stratiform sediment hosted Zn–Pb–Ag deposits, often referred to as SEDEX deposits, represent an economically important class of ore, that have received relatively little attention in terms of defining lithochemical halos and geochemical vectors useful to exploration. This study concentrates on the Lady Loretta deposit which is a typical example of the class of Proterozoic SEDEX deposits in northern Australia. We examined the major and trace element chemistry of carbonate-bearing sediments surrounding the deposit and defined a series of halos which extend for several hundred metres across strike and up to 1.5 km along strike. The stratiform ore lens is surrounded by an inner sideritic halo [Carr, G.R., 1984. Primary geochemical and mineralogical dispersion in the vicinity of the Lady Loretta Zn–Pb–Ag deposit, North Queensland. J. Geochem. Expl. 22, 217–238], followed by an outer ankerite/ferroan dolomite halo which merges with low iron dolomitic sediments representative of the regional background compositions. Carbonate within the inner siderite halo varies in composition from siderite to pistomesite (Fe_0.6Mg_0.4CO₃), whereas carbonate in the outer ankerite halo varies from ferroan dolomite to ankerite (Ca_0.5Mg_0.3Fe_0.2CO₃). Element dispersion around the stratiform ore lens is variable with Pb, Cu, Ba and Sr showing very little dispersion (<50 m across strike), Zn and Fe showing moderate dispersion (<100 m) and Mn and Tl showing broad dispersion (<200 m). Within the siderite halo Cu, Mg and Na show marked depletion compared to the surrounding sediments. The magnitude of element dispersion and change in carbonate chemistry around the Lady Loretta orebody has enabled the development of three geochemical vectors applicable to exploration. Whole rock analyses are used to calculate the three vector quantities as follows: (1) SEDEX metal index = Zn + 100Pb + 100Tl; (2) SEDEX alteration index = (FeO + 10MnO)100/(FeO + 10MnO + MgO); (3) manganese content of dolomite: MnO_d = (MnO × 30.41)/CaO. All three vectors increase to ore both across strike and along strike. The manganese content of dolomite (MnO_d) exhibits the most systematic pattern increasing from background values of about 0.2 wt% to a maximum of around 0.6 wt% at the boundary between the ankerite and siderite halos. Siderite within the inner halo contains considerably more Mn with MnO values of 0.4 to 4.0 wt%. It is suggested here that the basket of indices defined at Lady Loretta (Zn, Tl, metal index, alteration index, MnO_d and MnO_s) is applicable in the exploration for stratiform Zn–Pb–Ag deposits in dolomite-rich sedimentary basins generally. The indices defined can firstly assist in the identification of sedimentary units favourable for SEDEX mineralisation, and secondly provide vectors along these units to ore. The alteration index and MnO_d, however, should only be used for exploration dolomitic sequences; they are not recommended for exploration in clastic sequences devoid of carbonates.     

东天山康古尔金矿床成矿物源的同位素地球化学特征

康古尔金矿床属晚古生代火山岩区剪切带蚀变岩型金矿。同位素地球化学研究表明,矿石中铅为正常铅,热液系统硫同位素组成为陨石硫型,矿石中碳、钕同位素组成具深源特征,同时矿石与火山岩围岩中的Ｓｉ、Ｓｒ、Ｓ、Ｐｂ等同位素组成相近,说明成矿物质主要来自矿体围岩———火山岩,晚期有少量来自矿区附近的侵入岩。铅、锶同位素组成反映成矿过程中也有少量壳源物质的加入。     

福建浦城上厂矿田铜钼多金属矿成矿预测研究

根据蚀变分带及矿物组合、矿田地球化学分带及元素组合特征,对矿床类型及成矿模型特征进行探讨。成岩与成矿作用在时空上总体具有由西南向东北迁移演化的特点,上厂矿段为中高温Mo（Cu、Pb、Zn）矿→金竹坑矿段为中低温Cu、Pb、Zn（Ag）矿→雷母寨矿段为中低温Ag、Pb、Zn矿。三者从时间、空间、物源等方面有依存关系,以及矿化类型专属性等,可以将矿田矿床划分斑岩型铜钼多金属矿床及火山-次火山热液型铅锌银多金属矿床2个成矿类型,并类比预测矿田矿化类型及找矿方向。