Multi-stage Ag–Bi–Co–Ni–U and Cu–Bi vein mineralization at Wittichen,Schwarzwald, SW Germany: geological setting,ore mineralogy,and fluid evolution

The Wittichen Co–Ag–Bi–U mining area (Schwarzwald ore district, SW Germany) hosts several unconformity-related vein-type mineralizations within Variscan leucogranite and Permian to Triassic redbeds. The multistage mineralization formed at the intersection of two fault systems in the last 250 Ma. A Permo-Triassic ore stage I with minor U–Bi–quartz–fluorite mineralization is followed by a Jurassic to Cretaceous ore stage II with the main Ag and Co mineralization consisting of several generations of gangue minerals that host the sub-stages of U–Bi, Bi–Ag, Ni–As–Bi and Co–As–Bi. Important ore minerals are native elements, Co and Ni arsenides, and pitchblende; sulphides are absent. The Miocene ore stage III comprises barite with the Cu–Bi sulfosalts emplectite, wittichenite and aikinite, and the sulphides anilite and djurleite besides native Bi, chalcopyrite, sphalerite, galena and tennantite. The mineral-forming fluid system changed from low salinity (<5 wt.% NaCl) at high temperature (around 300°C) in Permian to highly saline (around 25 wt.% NaCl + CaCl₂) at lower temperatures (50–150°C) in Triassic to Cretaceous times. Thermodynamic calculations and comparison with similar mineralizations worldwide show that the Mesozoic ore-forming fluid was alkaline with redox conditions above the hematite–magnetite buffer. We suggest that the precipitation mechanism for native elements, pitchblende and arsenides is a decrease in pH during fluid mixing processes. REE patterns in fluorite and the occurrence of Bi in all stages suggest a granitic source of some ore-forming elements, whereas, e.g. Ag, Co and Ni probably have been leached from the redbeds. The greater importance of Cu and isotope data indicates that the Miocene ore stage III is more influenced by fluids from the overlying redbeds and limestones than the earlier mineralization stages.     

Genesis of the Au–Bi–Cu–As, Cu–Mo ± W, and base–metal Au–Ag mineralization at the Mountain Freegold (Yukon, Canada): constraints from Ar–Ar and Re–Os geochronology and Pb and stable isotope compositions

The genesis of mineralized systems across the Mountain Freegold area, in the Dawson Range Cu–Au?±?Mo Belt of the Tintina Au province was constrained using Pb and stable isotope compositions and Ar–Ar and Re–Os geochronology. Pb isotope compositions of sulfides span a wide compositional range (²⁰⁶Pb/²⁰⁴Pb, 18.669–19.861; ²⁰⁸Pb/²⁰⁴Pb, 38.400–39.238) that overlaps the compositions of the spatially associated igneous rocks, thus indicating a magmatic origin for Pb and probably the other metals. Sulfur isotopic compositions of sulfide minerals are broadly similar and their δ³⁴S (Vienna-Canyon Diablo Troilite (V-CDT)) values range from ?1.4 to 3.6 ‰ consistent with the magmatic range, with the exception of stibnite from a Au–Sb–quartz vein, which has δ³⁴S values between ?8.1 and ?3.1 ‰. The δ³⁴S values of sulfates coexisting with sulfide are between 11.2 and 14.2 ‰; whereas, those from the weathering zone range from 3.7 to 4.3 ‰, indicating supergene sulfates derived from oxidation of hypogene sulfides. The δ¹³C (Vienna Peedee Belemnite (VPDB)) values of carbonate range from ?4.9 to 1.1 ‰ and are higher than magmatic values. The δ¹⁸O (V-SMOW) values of magmatic quartz phenocrysts and magmatic least-altered rocks vary between 6.2 and 10.1 ‰ and between 5.0 and 10.1 ‰, respectively, whereas altered magmatic rocks and hydrothermal minerals (quartz and magnetite) are relatively ¹⁸O-depleted (4.2 to 7.9 ‰ and ?6.3 to 1.5 ‰, respectively). Hydrogen isotope compositions of both least-altered and altered igneous rock samples are D-depleted (from ?133 to ?161 ‰ Vienna-Standard Mean Ocean Water (V-SMOW)), consistent with differential magma degassing and/or post-crystallization exchange between the rocks and meteoric ground water. Zircon from a chlorite-altered dike has a U–Pb crystallization age of 108.7?±?0.4 Ma; whereas, the same sample yielded a whole-rock Ar–Ar plateau age of 76.25?±?0.53 Ma. Likewise, molybdenite Re–Os model ages range from 75.8 to 78.2 Ma, indicating the mineralizing events are genetically related to Late Cretaceous volcano-plutonic intrusions in the area. The molybdenite Re–Os ages difference between the nearby Nucleus (75.9?±?0.3 to 76.2?±?0.3 Ma) and Revenue (77.9?±?0.3 to 78.2?±?0.3 Ma) mineral occurrences suggests an episodic mineralized system with two pulses of hydrothermal fluids separated by at least 2 Ma. This, in combination with geological features suggest the Nucleus deposit represents the apical and younger portion of the Revenue–Nucleus magmatic-hydrothermal system and may suggest an evolution from the porphyry to the epithermal environments.     

Cretaceous–Tertiary convergence and continental collision,Sanandaj–Sirjan Zone,western Iran

The Sanandaj–Sirjan Zone contains the metamorphic core of the Zagros continental collision zone in western Iran. The zone has been subdivided into the following from southwest to northeast: an outer belt of imbricate thrust slices (radiolarite, Bisotun, ophiolite and marginal sub-zones, which consist of Mesozoic deep-marine sediments, shallow-marine carbonates, oceanic crust and volcanic arc, respectively) and an inner complexly deformed sub-zone (late Palaeozoic–Mesozoic passive margin succession). Rifting and sea-floor spreading of Tethys occurred in the Permian to Triassic but in the Sanandaj–Sirjan Zone extension-related successions are mainly of Late Triassic age. Subduction of Tethyan sea floor in the Late Jurassic to Cretaceous produced deformation, metamorphism and unconformities in the marginal and complexly deformed sub-zones. Deformation climaxed in the Late Cretaceous when a major southwest-vergent fold belt formed associated with greenschist facies metamorphism and post-dated by abundant Palaeogene granitic plutons. In the southwest of the zone a Late Cretaceous island arc—passive margin collision occurred with ophiolite emplacement onto the northern Arabian margin similar to that in Oman. Final closure of Tethys was not completed until the Miocene when Central Iran collided with the northeast Arabian margin.     

Petrogenesis of the Bao'anzhai granite and associated Mo mineralization,western Dabie orogen,east-central China: Constraints from zircon U–Pb and molybdenite Re–Os dating,whole-rock geochemistry,and Sr–Nd–Pb–Hf isotopes

Recently, many Mo deposits genetically related to emplacement of Early Cretaceous granites have been found in the Dabie–Qinling belt. A typical intrusion that combines magmatism and metallogenesis, the Bao'anzhai granite, yields a zircon ²³⁸U–²⁰⁶Pb age of 123.2 ± 1.1 Ma and a molybdenite Re–Os isochron age of 122.5 ± 2.7 Ma. This granite is characterized by high silica and alkali, but low Mg, Fe, and Ca. It is enriched with light rare earth elements (REEs) and large-ion lithophile elements (LILEs, Rb, K, Th, U) but depleted of heavy REEs, high field strength elements (HFSEs, Nb, Ta, Ti, and Y), and Sr. This high-K granite has medium initial ⁸⁷Sr/⁸⁶Sr ratios (0.706518–0.707116) and low initial Pb isotopic ratios [(²⁰⁶Pb/²⁰⁴Pb)_i, 16.423–16.699; (²⁰⁷Pb/²⁰⁴Pb)_i, 15.285–15.345; (²⁰⁸Pb/²⁰⁴Pb)_i, 37.335–37.633], and is characterized by low ?_Nd(t) and ?_Hf(t) values (?14.92 to??14.22 and??21.67 to??19.19, respectively). These data indicate that this pluton is a high-K calc-alkaline fractionated I-type granitite. It was generated by partial melting of the Yangtze lower crust, which is probably similar to Neoproterozoic TTG-like magmatic rocks at the north Yangtze Block under a non-thickened lower crust environment (<35 km). The ores also have low radiogenic Pb isotopes (²⁰⁶Pb/²⁰⁴Pb, 16.592–17.674; ²⁰⁷Pb/²⁰⁴Pb, 15.300–15.476; ²⁰⁸Pb/²⁰⁴Pb, 37.419–37.911) and low Re content in molybdenite (5.693–10.970 ppm), suggesting a crustal magmatic source for the metallogenic minerals in the Mo deposit.     

Geochronology,geochemistry and Sr–Nd–Hf–S–Pb isotopes of the Early Cretaceous Taoxihu Sn deposit and related granitoids,SE China

The Taoxihu deposit (eastern Guangdong, SE China) is a newly discovered Sn polymetallic deposit. Zircon U-Pb dating yielded 141.8 ± 1.0 Ma for the Sn-bearing granite porphyry and 145.5 ± 1.6 Ma for the biotite granite batholith it intruded. The age of the granite porphyry is consistent (within error) with the molybdenite Re–Os isochron age (139.0 ± 1.1 Ma) of the Sn mineralization, indicating a temporal link between the two. Geochemical data show that the granite porphyry is weakly peraluminous, contain high Si, Na and K, low Fe, Mg, Ca and P, and relatively high Rb/Sr and low K/Rb values. The rocks are enriched in Rb, Th, U, K, and Pb and depleted in Ba, Sr, Ti and Eu, resembling highly fractionated I-type granites. They contain bulk rock initial ⁸⁷Sr/⁸⁷Sr of 0.707371–0.707730 and εNd(t) of −5.17 to −4.67, and zircon εHf(t) values from −6.67 to −2.32, with late Mesoproterozoic T_DM2 ages for both Nd and Hf isotopes. This suggests that the granite porphyry was likely formed by the partial melting of the crustal basement of Mesoproterozoic overall residence age with minor mantle input.δ³⁴S_CDT values of the Taoxihu chalcopyrite and pyrite range from 0.1 to 2.1‰ (average: 0.9‰), implying a dominantly magmatic sulfur source. The ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb ratios of the Taoxihu sulfide ores are 18.497–18.669, 15.642–15.673 and 38.764–38.934, respectively, indicating a mainly upper continental crustal lead source with minor mantle contribution. The highly fractionated and reduced (low calculated zircon Ce⁴⁺/Ce³⁺ and Eu_N/Eu_N¹ values) nature of the ore-forming granitic magma may have facilitated the Sn enrichment and played a key role in the Sn mineralization. We propose that the ore-forming fluids at Taoxihu were of magmatic-hydrothermal origin derived from the granite porphyry, and that both the granite porphyry and the Sn mineralization were likely formed in an extensional setting, possibly related to the subduction slab rollback of the Paleo-Pacific Plate.     

Comparative Study of Gacun and Youre Silver–Lead–Zinc–Copper Deposits in Sichuan, SW China, and their Mineralization Significance

The large Gacun silver–lead–zinc–copper deposit in Sichuan Province is one of the largest volcanogenic massive sulfide(VMS) deposits in China. The deposit consists of western and central ore bodies, which form a vein–stockwork mineralization system corresponding to hydrothermal channels, and eastern ore bodies, which form an exhalative chemical sedimentary system derived from a brine pool in a submarine basin. The Youre lead–zinc deposit, which is currently under exploration and lies adjacent to the southern part of the Gacun deposit, is characterized by intense silicification and vein–stockwork structures and consists of massive silicified rhyolitic volcanics, banded rhyolitic tuff, and phyllitic sericite tuff. From a comparison of their ore-bearing horizons, the Gacun and Youre deposits have a continuous and stable hanging wall(calcareous slate and overlying andesite) and foot wall(rhyolite–dacite breccia and agglomerate), and the lithologic sequence includes lower intermediate to felsic rocks and upper felsic rocks. Thus, the Youre deposit, which comprises relatively thinly layered low–grade ore, is regarded as forming a southward extension of the Gacun deposit. A further comparison of the structures of the ore-bearing belts between the two deposits suggests that the Youre ore bodies are similar to the western ore bodies of the Gacun deposit. Moreover, the characteristics of fluid inclusions and stable isotopes in the Youre deposit are also similar to those of the western ore bodies of the Gacun deposit. Genetic models of the deposits are proposed for the Gacun–Youre ore district, and massive concealed ore bodies may occcur in the Youre deposit at depths that are similar to those of the eastern ore bodies of the Gacun deposit.     

Scale,causality, and the new organism–environment interaction

The fallout from environmental determinism of the early 20th century steered geography away from biological and evolutionary thought. Yet it also set in motion the diversification of how geographers conceive environment, how these environments shape and are shaped by humans, and how scaling negotiates the interpretation of this causality. I illustrate how this plurality of scalar perspectives and practices in geography is embedded in the organism–environment interaction recently articulated in the life sciences. I describe the new fields of epigenetics and niche construction to communicate how ideas about scale from human and physical geography come together in the life sciences. I argue that the two subdisciplinary modes or ‘moments’ of scalar thinking in geography are compatible, even necessary, through their embodiment in organisms. To procure predictability, organisms practice an epistemological scaling to rework the mental and material boundaries and scales in their environment. Yet organisms are also embedded in ontological flux. Boundaries and scales do not remain static because of the agency of other organisms to shape their own predictability. I formally define biological scaling as arising from the interplay of epistemological and ontological moments of scale. This third moment of scale creates local assemblages or topologies with a propensity for persistence. These ‘lumpy’ material outcomes of the new organism–environment interaction have analogues in posthuman and new materialist geographies. They also give formerly discredited Lamarckian modes of inheritance a renewed, but revised acceptance. This article argues for a biological view of scale and causality in geography.     

Platinum Mineralization in Multimetal Gold–Polymetallic,Au–Bi,Cu–Mo Porphyry,Cu–Ni,Titanomagnetite, and Copper–Sulfide Ore Deposits and Occurrences of the Upper Amur Region (Far East,Russia)

New data on platinum mineralization in ores, metasomatic rocks, concentrates, and tailings and wastes of some gold–polymetallic, Au–Bi, Cu–Mo porphyry, Cu–Ni, and titanomagnetite ore deposits and occurrences of the Upper Amur Region are presented. The contents of platinoids, Au and Ag in multimetal ores of gold-polymetallic, Au–Bi, Cu–Mo porphyry, Cu–Ni, and titanomagnetite ore deposits and ore occurrences are given. In addition, recommendations on the necessity of continuing scientific studies, revision, and resampling works in the search for platinoids in other complex ores of deposits and occurrences of the Upper Amur Region are given.     

Origin of the Maoduan Pb–Zn–Mo deposit, eastern Cathaysia Block, China: geological, geochronological, geochemical, and Sr–Nd–Pb–S isotopic constraints

The Maoduan Pb–Zn–Mo deposit is in hydrothermal veins with a pyrrhotite stage followed by a molybdenite and base metal stage. The Re–Os model ages of five molybdenite samples range from 138.6 ± 2.0 to 140.0 ± 1.9 Ma. Their isochron age is 137.7 ± 2.7 Ma. Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) zircon U–Pb dating of the nearby exposed Linggen granite porphyry gave a ²⁰⁶Pb/²³⁸U age of 152.2 ± 2.2 Ma and the hidden Maoduan monzogranite yielded a mean of 140.0 ± 1.6 Ma. These results suggest that the intrusion of the Maoduan monzogranite and Pb–Zn–Mo mineralization are contemporaneous. δ ³⁴S values of sulfide minerals range from 3.4‰ to 4.8‰, similar to magmatic sulfur. Four sulfide samples have ²⁰⁶Pb/²⁰⁴Pb = 18.252–18.432, ²⁰⁷Pb/²⁰⁴Pb = 15.609–15.779, and ²⁰⁸Pb/²⁰⁴Pb = 38.640–39.431, similar to the age-corrected data of the Maoduan monzogranite. These isotope data support a genetic relationship between the Pb–Zn–Mo mineralization and the Maoduan monzogranite and probably indicate a common deep source. The Maoduan monzogranite has geochemical features similar to highly fractionated I-type granites, such as high SiO₂ (73.7–75.2 wt.%) and alkalis (K₂O + Na₂O = 7.8–8.9 wt.%) and low FeO_t (0.8–1.3 wt.%), MgO (~0.3 wt.%), P₂O₅ (~0.03 wt.%), and TiO₂ (~0.2 wt.%). The granitic rocks are enriched in Rb, Th, and U but depleted in Ba, Sr, Nb, Ta, P, and Ti. REE patterns are characterized by marked negative Eu anomalies (Eu/Eu^* = 0.2–0.4). The Maoduan monzogranite, having (⁸⁷Sr/⁸⁶Sr) _t  = 0.7169 to 0.7170 and ε_Nd(t) = −13.8 to −13.7, was probably derived from mixing of partial melts from enriched mantle and the Paleoproterozoic Badu group in an extensional tectonic setting.     

Geochronology,geochemistry, Sr–Nd–Hf isotopic compositions,and petrogenetic and tectonic implications of Early Cretaceous intrusions associated with the Duolong porphyry–epithermal Cu–Au deposit,central Tibet

This article reports new zircon laser ablation-multicollector-inductively coupled plasma-mass spectrometry U–Pb and Hf isotope, whole-rock major and trace element, and Sr–Nd isotope data for mineralized and barren intrusions associated with the Duolong porphyry–epithermal copper–(gold) deposit (DPCD, a mining camp containing several individual deposits) in the western Qiangtang Terrane (QT), central Tibet. These data are used to further our understanding of the geological evolution of this region. The mineralized and barren DPCD intrusions are typical I-type granitoids that were synchronously emplaced at ca. 112.6–125.9 Ma. These igneous rocks show arc affinities that are characterized by enrichments in the light rare earth elements (La_N/Yb_N = 4.08–15.23) and the light ion lithophile elements (Rb, Th, U, K, and Pb), and depletions in the high field strength elements (Nb, Ta, and Ti). They have ⁸⁷Sr/⁸⁶Sr_(i) values of 0.7046–0.7079, _Nd(t) values of –6.0 to +1.1, and two-stage Nd model ages of ca. 823–1410 Ma. Zircons from these intrusive rocks have variable but generally positive ε_Hf(t) values (–2.7 to +13.7) and relatively young zircon Hf crustal model ages of 335–1351 Ma. Combining these data with geochemical data reported in recent studies, we infer that the mineralized and barren DPCD intrusions formed in a continental marginal arc setting and likely originated from a common parental magma that was result of magma mixing of juvenile crust-derived basaltic melts and old lower crust-derived melts. The formation of the DPCD intrusions indicates that the Bangongco–Nujiang oceanic lithosphere was still undergoing northward subduction beneath the western QT at ca. 112.6–125.9 Ma, suggesting in turn that the oceanic basin have not closed completely during the Early Cretaceous. These new data also indicate that the processes that occur during the subduction of oceanic crust in continental marginal arc settings produce and preserve juvenile crustal material, leading to net continental crust vertical growth and thickening.     

Chemical composition of rock-forming minerals in granitoids associated with Au–Bi–Cu,Cu–Mo,and Au–Ag mineralization at the Freegold Mountain,Yukon, Canada: magmatic and hydrothermal fluid chemistry and petrogenetic implications

The chemical compositions of rock-forming minerals have been determined for both altered and least-altered igneous rocks spatially associated with numerous mineralized zones (Nucleus Au–Bi–Cu–As deposit, Revenue Au ± Cu and Stoddart Cu–Mo ± W mineral occurrences, and Laforma Au–Ag deposit) across the Freegold Mountain area, Yukon, Canada. Within the study area, K-feldspar has a narrow compositional range (89.4–91% Or), whereas plagioclase spans a wide range (4.4–70.07% An). In all of the investigated samples, T _Ab = T _An = T _Or, suggesting that magmatic equilibrium between the coexisting plagioclase and K-feldspar was maintained. Igneous amphibole phenocrysts from hypabyssal dikes are typically calcic, whereas the Stoddart Cu–Mo ± W, Laforma Au–Ag, and Goldy Au mineralization are associated with Mg-enriched primary amphibole of edenite composition, and Au–Bi–Cu–As mineralization from Nucleus is related to Al-enriched primary amphibole of ferropargasite composition. Primary biotite phenocrysts across the Freegold Mountain area re-equilibrated with oxidized magma (f(O₂) values between 10–13 and 10–11.5 bars, lying between the Ni/NiO and the magnetite/haematite buffers). However, biotite and amphibole phenocrysts from Stoddart, Goldy, Laforma, and the Highway zones crystallized from a more oxidized magma, as indicated by their elevated X _Mg up to 0.65, relative to biotite and hornblende from Nucleus and Revenue characterized by a lower X _Mg (typically < 0.50). This suggests that various sources and (or) rapid emplacement were involved in magma genesis, as further supported by the considerable variation of pressure (1.8–7.3 kb) of amphibole crystallization and of the total Al content in least-altered biotite (2.6–2.9 afu) within the Freegold Mountain area. Biotite and apatite equilibrated within the T range of 520–780°C, consistent with temperatures of equilibration between ilmenite and magnetite, and their compositions indicate that they formed from an oxidized I-type magma. Magma differentiated by fractional crystallization (indicated by the presence of normally zoned plagioclase with Ca-rich cores and Na-enriched outer rims) and multiple magma mixing (supported by the presence of reversed zoned plagioclase and coexistence of normally and reversely zoned plagioclase). Lower X _Mg biotite associated with the mineralized (Cu–Mo ± W) potassic alteration incorporated more F and Cl relative to least-altered biotite with higher X _Mg. In both Nucleus and Revenue Au–Cu mineralizations, secondary biotite composition varies with respect to the associated alteration mineral assemblages. Although secondary biotite in the skarn re-equilibrated with F-poor fluids, secondary biotite from the pervasive biotitization is related to F- and Cl-enriched fluids, and secondary biotite from the phyllitic zone is related to F-, Cl-, and Mg-depleted fluids, thus consistent with a change in mineralizing fluid composition during mineralization.     

Re–Os and U–Pb geochronology of the Duobaoshan porphyry Cu–Mo–(Au) deposit,northeast China,and its geological significance

The large-scale Duobaoshan porphyry Cu–Mo–(Au) deposit is located at the north segment of the Da Hinggan Mountains, northeast China. Six molybdenite samples from the Duobaoshan deposit were selected for Re–Os isotope measurement to define the mineralization age of the deposit, yieldings a Re–Os isochron age of 475.9 ± 7.9 Ma (2σ), which is accordant with the Re–Os model ages of 476.6 ± 6.9–480.2 ± 6.9 Ma. This age is consistent with the age of the related granodiorite porphyry, which was dated as 477.2 ± 4 Ma by zircon U–Pb analysis using LA-ICP-MS. These ages disagree with the previous K–Ar age determinations that suggest a correlation of intrusive rocks of the Duobaoshan area with the Hercynian intrusive rocks of Carboniferous–Permian age. These ages demonstrate that the Duobaoshan granodiorite porphyry and related Cu–Mo deposit occurred in the Early Ordovician. The rhenium content of molybdenite varies from 290.9 to 728.2 μg/g, with an average content of 634.8 μg/g. The high rhenium content in molybdenite of the Duobaoshan deposit suggests that the ore-forming materials may be mainly of mantle source.     

Ruby–sapphire–spinel mineralization in marble of the middle and southern Urals: Geology,mineralogy, and genesis

Ruby and spinel occurrences hosted in marble on the eastern slope of the Urals are considered. Ruby- and spinel-bearing marble is a specific rock in granite-gneiss complexes of the East Ural Megazone, which formed at the Late Paleozoic collision stage of the evolution of the Urals. Organogenic marine limestone is the protolith of the marble. No relict sedimentary bedding has been retained in the marble. The observed banding is a secondary phenomenon related to crystallization and is controlled by flow cleavage. Magnesian metasomatism of limestone with the formation of fine-grained dolomite enriched in Cr, V, Ti, Mn, Cu, Zn, Ga, and REE took place at the prograde stage of metamorphism. Dedolomitization of rocks with the formation of background calcite marble also developed at the prograde stage. Mg-calcite marble with spinel and ruby of the first type formed in the metamorphic fluid circulation zone. Magnesian metasomatism with the formation of bicarbonate marble with ruby, pink sapphire, and spinel of the second type developed at the early retrograde stage. The formation of mica-bearing mineralized zones with corundum and spinel of the third type controlled by cleavage fractures is related to the pneumatolytic–hydrothermal stage. The data on ruby-bearing marble in the Urals may be used for forecasting and prospecting of ruby and sapphire deposits hosted in marble worldwide.     

Mineralogical,petrological, and geochemical studies of the Limahe mafic–ultramatic intrusion and associated Ni–Cu sulfide ores,SW China

The Limahe Ni–Cu sulfide deposit is hosted by a small mafic–ultramafic intrusion (800 × 200 × 300 m) that is temporally associated with the voluminous Permian flood basalts in SW China. The objective of this study is to better understand the origin of the deposit in the context of regional magmatism which is important for the ongoing mineral exploration in the region. The Limahe intrusion is a multiphase intrusion with an ultramafic unit at the base and a mafic unit at the top. The two rock units have intrusive contacts and exhibit similar mantle-normalized trace element patterns and Sr–Nd isotopic compositions but significantly different cumulus mineralogy and major element compositions. The similarities suggest that they are related to a common parental liquid, whereas the differences point to magma differentiation by olivine crystallization at depth. Sulfide mineralization is restricted to the ultramafic unit. The abundances of sulfides in the ultramafic unit generally increase towards the basal contacts with sedimentary footwall. The δ ³⁴S values of sulfide minerals from the Limahe deposit are elevated, ranging from +2.4 to +5.4‰. These values suggest the involvement of external S with elevated δ ³⁴S values. The mantle-normalized platinum-group element (PGE) patterns of bulk sulfide ores are similar to those of picrites associated with flood basalts in the region. The abundances of PGE in the sulfide ores, however, are significantly lower than that of sulfide liquid expected to segregate from undepleted picrite magma. Cr-spinel and olivine are present in the Limahe ultramafic rocks as well as in the picrites. Mantle-normalized trace element patterns of the Limahe intrusion generally resemble those of the picrites. However, negative Nb–Ta anomalies, common features of contamination with the lower or middle crust, are present in the intrusion but absent in the picrites. Sr–Nd isotopes suggest that the Limahe intrusion experienced higher degrees of contamination with the upper crust than did the picrites. The results of this study permit us to suggest that the parental magma of the Limahe intrusion was derived from picritic magma by olivine fractionation and contamination in a staging chamber at mid-crustal levels. Depletion of PGE in the sulfide ores in the Limahe intrusion is likely due to previous sulfide segregation of the parental magmas in the staging chamber. Sulfide mineralization in the Limahe intrusion is related to second-stage sulfide segregation after the fractionated magmas acquired external S from pyrite-bearing country rocks during magma ascent to the Limahe chamber. The abrupt change in mineralogical and chemical compositions between the ultramafic unit and the overlying unit suggests that at least two separate pulses of magma were involved in the development of the Limahe intrusion. We propose that the Limahe intrusion was once a wider part of a dynamic conduit that fed magma to the overlying subvolcanic dykes/sills or lavas. The ultramafic unit formed by the first, relatively more primitive magma, and the mafic unit formed by the second, relatively more fractionated magma. Immiscible sulfide droplets that segregated from the first magma settled down with olivine crystals to form the sulfide-bearing, olivine-rich rocks in the base of the intrusion. The overlying residual liquids were then pushed out of the chamber by the second magma. Critical factors for the formation of an economic Ni–Cu sulfide deposit in such a small intrusion include the dynamic petrologic processes involved and the availability of external sulfur. The Limahe deposit reminds us that small, multiphase, mafic–ultramafic intrusions in the region should not be overlooked for the potential of economic Ni–Cu sulfide deposits.     

Geochronology,geochemistry and Sr–Nd–Hf isotopes of the Haisugou porphyry Mo deposit,northeast China,and their geological significance

The Haisugou Mo deposit is located in the northern part of the Xilamulun Mo–Cu metallogenic belt in northeastern China. The Mo mineralization mainly occurs as quartz-molybdenite veins within the Haisugou granite, which was emplaced into rocks of the Early Permian Qingfengshan Formation. Zircon U–Pb dating by LA–ICP-MS of the granite yields a crystallization age of 137.6 ± 0.9 Ma, suggesting emplacement during the peak time of Mo mineralization in eastern China, broadly constrained to ca. 150–130 Ma, when tectonic stresses shifted from compression to extension. Whole-rock geochemical data suggest that the granite belongs to the high-K calc-alkaline series, and is characterized by relatively high LREE; low HREE; depletion of Ti, Ba, and Nb; and a moderate negative Eu anomaly. The zircon ε_Hf(t) and whole-rock ε_Nd(t) values for the intrusion range from +4.5 to +10.0 and +0.2 to +1.6, respectively, indicating that the magma originated from the juvenile lower crust source derived from depleted mantle, with some component of ancient continental crust. The granite is also characterized by initial (⁸⁷Sr/⁸⁶Sr)_i ratios ranging from 0.7040 to 0.7074, which suggest some contamination by the upper crust during the ascent of the primitive magma. Moreover, it can be recognized from the whole-rock major and trace element data that significant fractional crystallization occurred during magmatic evolution, with the separation of plagioclase and K-feldspar. Because Mo is an incompatible element and tends to concentrate in the melt during crystallization, fractionation processes likely played an important role in the formation of the Haisugou Mo deposit.     

Deformation,metamorphism, and mobilization of Ni–Cu–PGE sulfide ores at Garson Mine,Sudbury

The Garson Ni–Cu–platinum group element deposit is a deformed, overturned, low Ni tenor contact-type deposit along the contact between the Sudbury Igneous Complex (SIC) and stratigraphically underlying rocks of the Huronian Supergroup in the South Range of the 1.85-Ga Sudbury structure. The ore bodies are coincident with steeply south-dipping, north-over-south D₁ shear zones, which imbricated the SIC, its ore zones, and underlying Huronian rocks during mid-amphibolite facies metamorphism. The shear zones were reactivated as south-over-north, reverse shear zones during D₂ at mid-greenschist facies metamorphism. Syn-D₂ metamorphic titanite yields an age of 1,849?±?6 Ma, suggesting that D₁ and D₂ occurred immediately after crystallization of the SIC during the Penokean Orogeny. The ore bodies plunge steeply to the south parallel to colinear L₁ and L₂ mineral lineations, indicating that the geometry of the ore bodies are strongly controlled by D₁ and D₂. Sulfide mineralization consists of breccia ores, with minor disseminated sulfides hosted in norite, and syn-D₂ quartz–calcite–sulfide veins. Mobilization by ductile plastic flow was the dominant mechanism of sulfide/metal mobilization during D₁ and D₂, with additional minor hydrothermal mobilization of Cu, Fe, and Ni by hydrothermal fluids during D₂. Metamorphic pentlandite overgrows a S₁ ferrotschermakite foliation in D₁ deformed ore zones. Pentlandite was exsolved from recrystallized polygonal pyrrhotite grains after cessation of D₁, which resulted in randomly distributed large pentlandite grains and randomly oriented pentlandite loops along the grain boundaries of polygonal pyrrhotite within the breccia ore. It also overgrows a S₂ chlorite foliation in D₂ shear zones. Pyrrhotite recrystallized and was flattened during D₂ deformation of breccia ore along narrow shear zones. Exsolution of pentlandite loops along the grain boundaries of these flattened grains produced a pyrrhotite–pentlandite layering that is not observed in D₁ deformed ore zones. The overprinting of the two foliations by pentlandite and exsolution of pentlandite along the grain boundaries of flattened pyrrhotite grains suggest that the Garson ores reverted to a metamorphic monosulfide solid solution at temperatures ranging between 550 and 600 °C during D₁ and continued to deform as a monosulfide solid solution during D₂.     

Re–Os and U–Pb Geochronology of the Erlihe Pb–Zn Deposit, Qinling Orogenic Belt, Central China, and Constraints on Its Deposit Genesis

The Erlihe Pb–Zn deposit is an important mine of the Pb–Zn metallogenic zone in the South Qinling Orogen. It has been considered a sedimentary exhalative deposit in previous investigations because the ore body occurs concordantly at the transitional location of an upright fold. Re and Os isotopic analyses for paragenetic pyrites with sphalerite and galena from the ore body have been used to determine the timing of mineralization and to trace the source of metallogenic materials. The Re–Os isotopic data of four pyrite samples construct an isochron, yielding a weighted average age of 226±17 Ma (mean square weighted deviation=1.7), which is considered the main mineralization age. A dioritic porphyrite vein sample, showing weaker mineralization, was also dated using the SHRIMP zircon U–Pb isotopic method to constrain the youngest metallogenic age of the ore deposit, because it distributes along a group of tensional joints cutting not only the upright fold in the deposit field, but also the main ore bodies. The dioritic porphyrite sample yields a weighted mean 206Pb/238U age of 221±3 Ma, which is slightly younger than the Re–Os isotopic isochron age of the pyrites, considered as the upper age limit of the mineralization, namely the ending age of the mineralization. The Os isotopic compositions of sulfide minerals distribute within a range between Os isotopic compositions of the crust and the mantle, indicating that the ore deposit can be derived from magma-related fluid, and the metallogenic materials are most likely derived from the mixing source of the crust and the mantle. The Erlihe Pb–Zn deposit and associated dioritic porphyrite vein, important records of Qinling tectonic–magmatism–mineralization activities, were formed during the Triassic collisional orogeny processes.     

U–Pb and Ar–Ar geochronology of the Fujiawu porphyry Cu–Mo deposit,Dexing district,Southeast China: Implications for magmatism,hydrothermal alteration,and mineralization

The Fujiawu porphyry Cu–Mo deposit is one of several porphyry Cu–Mo deposits in the Dexing district, Jiangxi Province, Southeast China. New zircon SHRIMP U–Pb data yield a weighted mean ²⁰⁶Pb/²³⁸U age of 172.0 ± 2.1 and 168.5 ± 1.4 Ma from weakly altered granodiorite porphyry and quartz diorite porphyry, respectively. Two hydrothermal biotites from granodiorite porphyry give an Ar–Ar step-heating plateau age of 169.9 ± 1.8 and 168.7 ± 1.8 Ma. Hydrothermal apatite exsolved from altered biotite yields an isotope dilution thermal ionization mass spectrometry isochron age of 164.4 ± 0.9 Ma. The apatite age is similar to the ages obtained from hydrothermal rutile (165.0 ± 1.1 and 164.8 ± 1.6 Ma) and indicates that the magmatism and hydrothermal activity in the Fujiawu deposit occurred in the Middle Jurassic. Hydrothermal fluid circulation related to multiple stages of magma emplacement resulted in Cu–Mo mineralization in the Fujiawu porphyry deposit. The zircon SHRIMP U–Pb ages and the published molybdenite Re–Os age (170.9 ± 1.5 Ma) represent the timing of magma crystallization and Mo mineralization, whereas the rutile and apatite U–Pb ages reflect the timing of Cu mineralization following quartz diorite emplacement. The data suggest slow cooling after emplacement of the quartz diorite porphyry.     

The P–T–t paths of high-grade gneisses,Kaoko Belt,Namibia: Constraints from mineral data,U–Pb allanite and monazite and Sm–Nd/Lu–Hf garnet ages and garnet ion probe data

The Damara Orogeny is a late Neoproterozoic to Cambrian (ca. 570–480 Ma) intracratonic event that affected the Kaoko Belt, the inland branch of the Damara orogen and the Gariep Belt in Namibia and South Africa. This study focuses on the Pan-African evolution of part of the Kaoko Belt between the Puros shear zone and the Village mylonite zone which consists of Mesoproterozoic migmatitic para- and orthogneisses with minor granulite and amphibolite. Pseudosection modeling combined with thermobarometric calculations indicate that the para- and orthogneisses equilibrated at about 670–800 °C and ca. 0.6–0.8 GPa. Some garnets display a pronounced bell-shaped Ca, HREE, Y and Sr zoning, flat zoning profiles of Mn and Fe and concave upward concentration profiles of Sm and Nd. Pressure–temperature estimates obtained on these garnets reveal similar temperatures of 700–750 °C but slightly higher pressures of ca. 0.9 GPa. The preservation of distinct major and trace element zoning in garnet and the existence of broadly similar (near prograde) Sm–Nd and Lu–Hf garnet–whole rock ages of ca. 525 Ma obtained on the same sample indicate an extremely fast cooling path. Retrograde conditions persisted until ca. 490 Ma indicating a slow, late stage near isobaric cooling path. The resulting clockwise P–T–t path is consistent with crustal thickening through continent–continent collision followed by post-collisional extension and suggests that the upper amphibolite to granulite facies terrain of the central Kaoko Belt formed initially in a metamorphic field gradient of ca. 25–35 °C km^− 1 at moderately high pressures.