Ore metal redistribution by hydrocarbon–brine and hydrocarbon–halide melt phases, North Range footwall of the Sudbury Igneous Complex, Ontario, Canada

We report methane-dominant hydrocarbon (fluid) inclusions (CH₄±C₂H₆–C₂H₂, C₃H₈) coexisting with primary brine inclusions and secondary halide melt (solid NaCl) inclusions in Au–Pt-rich quartz-sulfide-epidote alteration veins associated with the footwall-style Cu–PGE (platinum-group element)–Au deposits at the Fraser Mine (North Range of the Sudbury Igneous Complex). Evidence for coentrapment of immiscible hydrocarbon–brine, and hydrocarbon–halide melt mixtures is demonstrated. A primary CH₄–brine assemblage was trapped during quartz growth at relatively low T (min. T _trapping∼145–315°C) and P (max. P _trapping∼500 bar), prior to the crystallization of sulfide minerals in the veins. Secondary inclusions contain solid halite and a mixture of CH₄, C₂H₆–C₂H₂ and C₃H₈ and were trapped at a minimum T of ∼710°C. The halite inclusions may represent halide melt that exsolved from crystallizing sulfide ores that texturally postdate (by replacement) early alteration quartz hosting the primary, lower T brine–CH₄ assemblage. Laser ablation ICP-MS analyses show that the brine, hydrocarbon and halide melt inclusions contain significant concentrations of Cu (0.1–1 wt% range), Au, Bi, Ag and Pt (all 0.1–10 ppm range). Cu:Pt and Cu:Au ratios in the inclusions are significantly (up to 4 log units) lower than in the host alteration veins and adjacent massive sulfide ore veins, suggesting either (1) early Cu loss from the volatiles by chalcopyrite precipitation or (2) enhanced Au and Pt solubilities relative to Cu at the temperatures of entrapment. Concentration ratios between coexisting brine and CH₄ inclusions are lower for Cu, Au, Bi and Ag than for other elements (Na, Ca, Fe, Mn, Zn, Pb) indicating that during interaction with the brine, the hydrocarbon phase was enriched in ore metals. The high concentrations of ore metals in hydrocarbon, brine and halide melt phases confirm that both aqueous and non-aqueous volatiles were carriers of precious metals in the Sudbury environment over a wide range of temperatures. Volatile evolution and magmatic sulfide differentiation were clearly part of a single, continuous process in the Sudbury footwall. The exsolution of H₂O-poor volatiles from fractionated sulfide liquid may have been a principal mechanism controlling the final distribution of PGE and Au in the footwall ore systems. The study reports the first measurements of precious metal concentrations in fluid inclusions from a magmatic Ni–Cu–PGE environment (the Sudbury district). Electronic Supplementary Material Supplementary material is available for this article at     

Hydrothermal alteration and Cu–Ni–PGE mobilization in the charnockitic rocks of the footwall of the South Kawishiwi intrusion,Duluth Complex,USA

In the Neoarchean (~ 2.7 Ga) contact metamorphosed charnockitic footwall of the Mesoproterosoic (1.1 Ga) South Kawishiwi intrusion of the Duluth Complex, the primary metamorphic mineral assemblage and Cu–Ni–PGE sulfide mineralization is overprinted by an actinolite + chlorite + cummingtonite + prehnite + pumpellyite + quartz + calcite hydrothermal mineral assemblage along 2–3 cm thick veins. In calcite, hosted by the hydrothermal alteration zones and in a single recrystallized quartz porphyroblast, four different fluid inclusion assemblages are documented; the composition of these fluid inclusions provide p–T conditions of the fluid flow, and helps to define the origin of the fluids and evaluate their role in the remobilization and reprecipitation of the primary metamorphic sulfide assemblage.Pure CO₂ fluid inclusions were found as early inclusions in recrystallized quartz porphyroblast. These inclusions may have been trapped during the recrystallization of the quartz during the contact metamorphism of the footwall charnockite in the footwall of the SKI. The estimated trapping pressure (1.6–2.0 kbar) and temperature (810–920 °C) conditions correspond to estimates based on felsic veins in the basal zones of the South Kawishiwi intrusion.Fluid inclusion assemblages with CO₂–H₂O–NaCl and CH₄–N₂–H₂O–NaCl compositions found in this study along healed microfractures in the recrystallized quartz porphyroblast establish the heterogeneous state of the fluids during entrapment. The estimated trapping pressure and temperature conditions (240–650 bar and 120–150 °C for CO₂–H₂O–NaCl inclusions and 315–360 bar and 145–165 °C for CH₄–N₂–H₂O–NaCl inclusions) are significantly lower than the p–T conditions (> 700 °C and 1.6–2 kbar) during the contact metamorphism, indicating that this fluid flow might not be related to the cooling of the Duluth Complex and its contact aureole. The presence of chalcopyrite inclusions in these fluid inclusions and in the trails of these fluid inclusion assemblages confirms that at least on local scale these fluids played a role in base metal remobilization. No evidences have been observed for PGE remobilization and transport in the samples. The source of the carbonic phase in the carbonic assemblages (CO₂; CH₄) could be the graphite, present in the metasedimentary hornfelsed inclusions in the basal zones of the South Kawishiwi intrusion.The hydrothermal veins in the charnockite can be characterized by an actinolite + cummingtonite + chlorite + prehnite + pumpellyite + calcite (I–II) + quartz mineral assemblage. Chlorite thermometry yields temperatures around 276–308 °C during the earliest phase of the fluid flow. In the late calcite (II) phase, high salinity (21.6–28.8 NaCl + CaCl₂ equiv. wt.%), low temperature (90–160 °C), primary aqueous inclusions were found. Chalcopyrite (± sphalerite ± millerite), replacing and intersecting the early hydrothermal phases, are associated to the late calcite (II) phase. The composition of the formational fluids in the Canadian Shield is comparable with the composition of the studied fluid inclusions. This suggests that the composition of the fluids did not change in the past 2 Ga and base metal remobilization by formational fluids could have taken place any time after the formation of the South Kawishiwi intrusion.Sulfur isotope studies carried out on the primary metamorphic (δ³⁴S = 7.4–8.9‰) and the hydrothermal sulfide mineral assemblage (δ³⁴S = 5.5–5.7‰) proves, that during the hydrothermal fluid flow the primary metamorphic ores were remobilized.     

Multi-stage hydrothermal processes involved in “low-sulfide” Cu(–Ni)–PGE mineralization in the footwall of the Sudbury Igneous Complex (Canada): Amy Lake PGE zone, East Range

The Amy Lake PGE zone is a “low-sulfide-type” Cu-(Ni-)PGE mineralization in the East Range footwall of the 1.85 Ga Sudbury Igneous Complex occurring in a 100-m-wide Sudbury Breccia belt that coincides with an impact-related major fracture zone (Bay Fault zone). Detailed hydrothermal alteration mapping, fluid inclusion, trace element, and stable isotope studies revealed a complex alteration and mineralization history in a multi-source, multi-stage Sudbury-related hydrothermal system. The two major stages of syn-Sudbury hydrothermal activity are characterized by similarly high-salinity, high-temperature fluids that are (1) locally derived from footwall granophyre bodies, and typified with high Ni/Cu and PGE/S ratios and high REE contents (magmatic–hydrothermal stage), and (2) a more voluminous Cu–Ni–PGE-rich fluid flux probably originated from the Sudbury Igneous Complex/footwall contact (hydrothermal stage). The second hydrothermal flux was introduced by brittle fractures in the area and resulted in a complex zonation of alteration assemblages and mineralization governed by local footwall composition. The Sudbury-related hydrothermal event was overprinted by shear-related epidote veining and calcite–chlorite replacement, both regionally present in the Sudbury structure. Based on analogies, the most important factors involved in the formation of hydrothermal low-sulfide mineralization are proposed to be (1) accumulation of PGE-enriched fluids, (2) large-scale brittle structures as conduits to these fluids, and (3) adequate host rock composition as a chemical trap resulting in sulfide and PGM precipitation. In environments meeting these criteria, hydrothermal PGE mineralization is known to have formed not only in the Sudbury footwall but also from mafic–ultramafic intrusions associated with primary magmatic PGE from several locations around the world.     

Formation of Ni–Cu–Platinum Group Element sulfide mineralization in the Sudbury Impact Melt Sheet

Summary The Ni–Cu–Platinum Group Element (PGE) sulfide deposits of the Sudbury Structure have provided a major portion of the worlds total nickel production and their host rocks have been the subject of numerous research studies, yet a number of perplexing problems remain to be solved. On the one hand, studies seeking to explain the formation of the Sudbury Structure have now converged on a genetic model which proposes that the Main Mass and Offset Dykes of the Sudbury Igneous Complex (SIC) were produced by crystallization of an impact-generated melt sheet. On the other hand, these models have yet to be fully reconciled with the production of the very large volume of magmatic Ni, Cu, Co, and PGE-rich sulfide mineralization and the associated mafic rock types. This paper explores this problem using new precious metal data from the Main Mass and Offset Dykes. These data are used to understand the relationships between these rocks, and to provide constraints on how the Ni–Cu–PGE sulfide ore deposits fit into the geological evolution of the Sudbury Structure.In the two drill cores selected for study in this project, the Mafic Norite has 1–5 modal percent pyrrhotite plus chalcopyrite, and elevated Ni (40–1000ppm), Cu (40–1140ppm), and PGE (1.9–7.8ppb Pd, 1.8–7.3ppb Pt); this is overlain by Felsic Norite that contains pyrrhotite, and has a wide range in concentration of Ni (13–257ppm), Cu (7–328ppm), and PGE (<0.01–6.4ppb Pd, <0.01–5ppb Pt). For a similar range of MgO, the upper portion of the Felsic Norite unit has 5–10 times lower Ni and Cu abundances than within-plate basalts and local crustal rocks, and PGE abundance levels are mostly below analytical determination limits. Stratigraphic studies of other compositional profiles around the SIC demonstrate that this depletion signature of Ni, Cu, and PGE is widespread and developed not only above mineralized embayments and offsets, but also above barren sections of the lower contact of the SIC.The depletion of the upper part of the Felsic Norite in Ni, Cu and PGE is presumably due to equilibration of the magma with magmatic sulfide, and accumulation of this dense sulfide liquid. Results of modeling indicate that the parental magma giving rise to the Mafic and Felsic Norites had initial Ni and Cu contents of 210 and 110ppm, respectively. In addition, Ni, Cu and PGE tenors calculated in 100% sulfide from the Copper Cliff Offset average 13% Cu, 6% Ni, 18ppm Pd, and 19ppm Pt indicating that these sulfides had formed by fractionation from magmas that contained 310ppm Ni, 310ppm Cu, 18ppb Pd and 19ppb Pt. These values are factors of 3 to 5 higher than the Ni, Cu, Pd, and Pt contents of the Onaping Formation with average values of 55ppm Ni, 48ppm Cu, and 4.9ppb Pd as well as the marginal sulfide-poor phase of the Worthington Offset quartz diorite, which has average values of 61ppm Ni, 59ppm Cu, 2.8ppb Pd and 4.0ppb Pt. Both the Onaping Formation and the marginal quartz diorite are believed to represent the initial composition of a large component of the melt sheet. There is therefore a fundamental problem in reconciling the initial metal contents of the SIC magma as indicated by the marginal phases of the Offset dykes and that of the Onaping Formation with the composition of the SIC magma at the times of formation of the sulfides as indicated by their Ni, Cu and PGE tenors.It is proposed that because the SIC melt sheet was initially superheated with a temperature of 1700°C, it was able to dissolve 5 times as much S as it could at its liquidus temperature of 1200°C. It was also initially composed of an emulsion of mafic and felsic melts (Marsh and Zieg, 1999), which may have formed discrete magma cells. As the temperature of the melt sheet decreased, some of these magma cells became S-saturated and the resultant Ni–Cu–PGE sulfides settled downwards and on reaching magma cells lower in the melt sheet were re-dissolved thereby raising the Ni, Cu and PGE contents of the lower magma cells. It was from these enriched magma cells that precipitation of the ore-forming Ni–Cu–PGE sulfide melts eventually took place.The mineral potential of Offset and embayment structures appears to be empirically linked to the thickness of the overlying noritic rocks; for example, the most heavily mineralized embayments and Offset Dykes are located in areas where the Felsic Norite is thickest. It appears unlikely that the entire 1–3km-thick melt sheet was convectively mixing throughout its lateral extent, and so the heterogeneity in sulfide distribution was retained after crystallization and cooling.     

Relationship between footwall composition,crustal contamination,and fluid–rock interaction in the Platreef,Bushveld Complex,South Africa

In the northern limb of the 2.06-Ga Bushveld Complex, the Platreef is a platinum group elements (PGE)-, Cu-, and Ni-mineralized zone of pyroxenite that developed at the intrusion margin. From north to south, the footwall rocks of the Platreef change from Archaean granite to dolomite, hornfels, and quartzite. Where the footwall is granite, the Sr-isotope system is more strongly perturbed than where the footwall is Sr-poor dolomite, in which samples show an approximate isochron relationship. The Nd-isotope system for samples of pyroxenite and hanging wall norite shows an approximate isochron relationship with an implied age of 2.17 ± 0.2 Ga and initial Nd-isotope ratio of 0.5095. Assuming an age of 2.06 Ga, the ɛNd values range from −6.2 to −9.6 (ave. −7.8, n = 17) and on average are slightly more negative than the Main Zone of the Bushveld. These data are consistent with local contamination of an already contaminated magma of Main Zone composition. The similarity in isotope composition between the Platreef pyroxenites and the hanging wall norites suggests a common origin. Where the country rock is dolomite, the Platreef has generally higher plagioclase and pyroxene δ ¹⁸O values, and this indicates assimilation of the immediate footwall. Throughout the Platreef, there is considerable petrographic evidence for sub-solidus interaction with fluids, and the Δ _{plagioclase–pyroxene} values range from −2 to +6, which indicates interaction at both high and low temperatures. Whole-rock and mineral δD values suggest that the Platreef interacted with both magmatic and meteoric water, and the lack of disturbance to the Sr-isotope system suggests that fluid–rock interaction took place soon after emplacement. Where the footwall is granite, less negative δD values suggest a greater involvement of meteoric water. Consistently higher values of Δ _{plagioclase–pyroxene} in the Platreef pyroxenites and hanging wall norites in contact with dolomite suggest prolonged interaction with CO₂-rich fluid derived from decarbonation of the footwall rocks. The overprint of post crystallization fluid–rock interaction is the probable cause of the previously documented lack of correlation between PGE and sulfide content on the small scale. The Platreef in contact with dolomite is the focus of the highest PGE grades, and this suggests that dolomite contamination played a role in PGE concentration and deposition, but the exact link remains obscure. It is a possibility that the CO₂ produced by decarbonation of assimilated dolomite enhanced the process of PGE scavenging by sulfide precipitation.     

Tremolite–calcite veins in the footwall of the Simplon Fault,Antigorio Valley,Lepontine Alps (Italy)

The lowermost units of the nappe pile of the Lepontine Alps crop out in the Antigorio valley in the footwall of the Simplon Fault. The whole orthogneiss section of the Antigorio Unit is exposed on both sides of the valley, sandwiched between the Mesozoic metasedimentary sequences of the Baceno unit below and the Tèggiolo unit above. The petrography and mineral composition of tremolite–calcite veins occurring in dolomite marble in both metasedimentary sequences were investigated. Tremolite–calcite (with lesser talc and minor phlogopite) veins have rhythmic banded texture. Banding is due to cyclic differences in modal abundances and fabric of tremolite and calcite. These veins are very similar to those occurring in dolomite rafts within the Bergell granite and it is inferred that they formed by the same “fracture-reaction-seal” mechanism. Veins formed by reaction of a silica-rich aqueous fluid with the host dolomite marble along fractures. According to thermo-barometric calculations, based on electron microprobe analyses, reaction occurred at temperatures between 450 and 490°C and minimum pressure of 2–3 kbar. Such temperature conditions occurred in this footwall region of the Simplon Fault Zone around 15 Ma, during exhumation and cooling of the nappe pile and a transition to brittle behaviour. Aqueous, silica-rich fluids concentrated along fractures, forming tremolite–calcite veins in the dolomite marbles and quartz veins in the orthogneiss.     

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.     

The distribution of platinum group elements (PGE) and other chalcophile elements among sulfides from the Creighton Ni–Cu–PGE sulfide deposit, Sudbury, Canada, and the origin of palladium in pentlandite

Concentrations of platinum group elements (PGE), Ag, As, Au, Bi, Cd, Co, Mo, Pb, Re, Sb, Se, Sn, Te, and Zn, have been determined in base metal sulfide (BMS) minerals from the western branch (402 Trough orebodies) of the Creighton Ni–Cu–PGE sulfide deposit, Sudbury, Canada. The sulfide assemblage is dominated by pyrrhotite, with minor pentlandite, chalcopyrite, and pyrite, and they represent monosulfide solid solution (MSS) cumulates. The aim of this study was to establish the distribution of the PGE among the BMS and platinum group minerals (PGM) in order to understand better the petrogenesis of the deposit. Mass balance calculations show that the BMS host all of the Co and Se, a significant proportion (40–90%) of Os, Pd, Ru, Cd, Sn, and Zn, but very little (<35%) of the Ag, Au, Bi, Ir, Mo, Pb, Pt, Rh, Re, Sb, and Te. Osmium and Ru are concentrated in equal proportions in pyrrhotite, pentlandite, and pyrite. Cobalt and Pd (∼1 ppm) are concentrated in pentlandite. Silver, Cd, Sn, Zn, and in rare cases Au and Te, are concentrated in chalcopyrite. Selenium is present in equal proportions in all three BMS. Iridium, Rh, and Pt are present in euhedrally zoned PGE sulfarsenides, which comprise irarsite (IrAsS), hollingworthite (RhAsS), PGE-Ni-rich cobaltite (CoAsS), and subordinate sperrylite (PtAs₂), all of which are hosted predominantly in pyrrhotite and pentlandite. Silver, Au, Bi, Mo, Pb, Re, Sb, and Te are found predominantly in discrete accessory minerals such as electrum (Au–Ag alloy), hessite (Ag₂Te), michenerite (PdBiTe), and rhenium sulfides. The enrichment of Os, Ru, Ni, and Co in pyrrhotite, pentlandite, and pyrite and Ag, Au, Cd, Sn, Te, and Zn in chalcopyrite can be explained by fractional crystallization of MSS from a sulfide liquid followed by exsolution of the sulfides. The early crystallization of the PGE sulfarsenides from the sulfide melt depleted the MSS in Ir and Rh. The bulk of Pd in pentlandite cannot be explained by sulfide fractionation alone because Pd should have partitioned into the residual Cu-rich liquid and be in chalcopyrite or in PGM around chalcopyrite. The variation of Pd among different pentlandite textures provides evidence that Pd diffuses into pentlandite during its exsolution from MSS. The source of Pd was from the small quantity of Pd that partitioned originally into the MSS and a larger quantity of Pd in the nearby Cu-rich portion (intermediate solid solution and/or Pd-bearing PGM). The source of Pd became depleted during the diffusion process, thus later-forming pentlandite (rims of coarse-granular, veinlets, and exsolution flames) contains less Pd than early-forming pentlandite (cores of coarse-granular).     

Rb–Sr and Sm–Nd study of granite–charnockite association in the Pudukkottai region and the link between metamorphism and magmatism in the Madurai Block

Pudukkottai region in the northeastern part of the Madurai Block exposes the garnetiferous pink granite that intruded the biotite gneiss. Charnockite patches are associated with both the rock types. Rb–Sr biotite and Sm–Nd whole-rock isochron ages indicate a regional uplift and cooling at ～550 Ma. The initial Nd isotope ratios (\(\varepsilon _{\text {Nd}}^{\mathrm {t}}=-20\) to ?22) and Nd depleted-mantle model ages (T_DM = 2.25 to 2.79 Ga) indicate a common crustal source for the pink-granite and associated charnockite, while the biotite gneiss and the charnockite within it represent an older crustal source (\(\varepsilon _{\text {Nd}}^{\mathrm {t}}= -29\) and T_DM = > 3.2 Ga). The Rb–Sr whole-rock data and initial Sr–Nd isotope ratios also help demonstrate the partial but systematic equilibration of Sr isotope and Rb/Sr ratios during metamorphic mineral-reactions resulting in an ‘apparent whole-rock isochron’. The available geochronological results from the Madurai Block indicate four major periods of magmatism and metamorphism: Neoarchaean–Paleoproterozoic, Mesoproterozoic, mid-Neoproterozoic and late-Neoproterozoic. We suggest that the high-grade and ultrahigh-temperature metamorphism was preceded by magmatism which ‘prepared’ the residual crust to sustain the high P–T conditions. There also appears to be cyclicity in the tectono-magmatic events and an evolutionary model for the Madurai Block should account for the cyclicity in the preserved records.     

Petrogenesis of the Mesoproterozoic (1.23?Ga) Sudbury dyke swarm and its questionable relationship to plate separation

The Mesoproterozoic (~1.23 Ga) Sudbury dyke swarm was emplaced at equatorial latitudes and cross-cuts the Grenville, Southern and Superior Provinces of the Canadian Shield. The dyke swarm has been linked to the break-up of the Mesoproterozoic supercontinent Columbia (1.8 to 1.3 Ga). The Sudbury dykes are alkaline olivine diabases that extend ~300 km to the W and NW from the Grenville Front. Major element trends and MELTS modeling indicate fractional crystallization of olivine and plagioclase. Detailed mineral chemical analyses across a 90-m-wide dyke shows a symmetric M-shaped pattern indicating vertical flow differentiation. The highest measured Fo value of olivine from the chilled margin of one dyke is 70, suggesting the parental magmas of the dykes were evolved. Unlike other dykes of the Canadian Shield, the Sudbury dykes do not show significant chemical variation across the length of the swarm. The Sudbury dykes have high Sr/Y (>10), La/Yb_N (>5) and Sm/Yb_PM (>2.4) values indicating they originated from a garnet-bearing source. The low Th/Nb (<1.5) values contrast with the low Nb/La (<0.6) and La/Ba (~0.4) values, suggesting a possible lithospheric mantle or subduction-modified mantle source. In the context of Grenvillian tectonics, the Sudbury dykes intruded the Laurentian craton and parautochthonous rocks. The dykes occupy pre-existing west to northwest trending faults, suggesting that they exploited regional structural heterogeneities during the closure of the Elzevir basin (i.e., 1,250 to 1,190 Ma). The alkaline composition, limited spatial-chemical variation, volume, geometry and regional geological context suggest that the dykes are not likely related to a mantle plume or the break-up of a supercontinent.     

Native Alloys of the Pd–Pt and Ni–Cu–Al Systems from the AS Luna-24

The close intergrowth of two native alloys of the compositions Ni_0.59Cu_0.24Al_0.15Fe_0.01Mn_0.01 and Pd_0.55Pt_0.36Rh_0.09 with a size of 10 μm has been discovered in the regolith from the Mare Crisium. A conclusion on its exhalative origin is made.     

The Ordovician Gabbro–Tonalite–Trondhjemite Complex and Associated Volcanic Rocks in the Paleozoic Suture between the Urals and Kazakhstan

Doklady Earth Sciences - This paper reports new data on the Early Ordovician age established for granitoids of the gabbro—tonalite–trondhjemite complex in the Denisovka ophiolite zone...     

Secondary alterations of globular and platy phyllosilicates of the glauconite–illite series in the Precambrian and Vendian–Cambrian rocks

Previously published and new data on secondary transformations of the globular and platy phyllosilicates of the glauconite–illite series from the Upper Proterozoic terrigenous rocks of the Olenek and Anabar uplifts (East Siberia), Srednii Peninsula (Murmansk coast), and Vendian–Cambrian boundary rocks of the Podolian Dniester area (Ukraine) are generalized for the first time. Plastic deformation, aluminization, chloritization, berthierinization, as well as replacement of phyllosilicates of different morphology by corrensite- chlorite and pyrite at different lithogenesis stages, are considered and lithological-mineralogical characteristics of the glauconite-bearing rocks are reported. The structural, crystal-chemical, genetic, and isotopegeochronological features of di- and trioctahedral phyllosilicates are discussed.     

Characteristics and Classification of the Geothermal Gradient in the Beijing–Tianjin–Hebei Plain,China

Mathematical Geosciences - Study of the characteristics and classification of geothermal gradients can effectively guide the exploration and development of geothermal resources. In this paper, we...     

The tectonics and stages of the geological history of the Yenisei–Khatanga Basin and the conjugate Taimyr Orogen

A new interpretation of the seismic profile series for the Taimyr Orogen and the Yenisei–Khatanga Basin is given in terms of their tectonics and geological history. The tectonics and tectonostratigraphy of the Yenisei–Khatanga and the Khatanga–Lena basins are considered. In the Late Vendian and Early Paleozoic, a passive continental margin and postrift shelf basin existed in Taimyr and the Yenisei–Khatanga Basin. From the Early Carboniferous to the Mid-Permian, the North and Central Taimyr zones were involved in orogeny. The Late Paleozoic foredeep was formed in the contemporary South Taimyr Zone. In the Middle to Late Triassic, a new orogeny took place in the large territory of Taimyr and the Noril’sk district of the Siberian Platform. A synorogenic foredeep has been recognized for the first time close to the Yenisei–Khatanga Basin. In the Jurassic and Early Cretaceous, this basin was subsided under transpressional conditions. Thereby, anticlinal swells were formed from the Callovian to the Aptian. Their growth continued in the Cenozoic. The Taimyr Orogen underwent tectonic reactivation and apparently right-lateral transpression from Carboniferous to Cenozoic.     

Shear deformation and strength of the interphase between the soil–rock mixture and the benched bedrock slope surface

A series of benched excavations were typically carried out on the bedrock slope surface to improve the stability of the soil–rock mixture (S–RM) fill slope. It is difficult to devise an in situ, large-scale direct shear test for the interphase between the S–RM fill and the benched bedrock slope surface. This study introduced a comprehensive approach to investigate the shear deformation and strength of the interphase. First the soil–rock distribution characteristics were analyzed by test pitting, image analysis, and sieve test. Then the PFC2D random structure models with different rock block size distributions were built, and large-scale numerical shear tests for the interphase were performed after calibrating model parameters through laboratory tests. The stress evolution, damage evolution and failure, deformation localization (based on a principle proposed in this paper), rotation of rock blocks, and shear strength were systematically investigated. It was found that as the rock block proportion and rock block size (rock block proportion of 50 %) increase, the fluctuations of the post-peak shear stress–displacement curves of the interphase become more obvious, and the shear band/localized failure path network becomes wider. Generally, smaller rock blocks are of greater rotation angles in the shear band. The peak shear stress and internal friction angle of the interphase increase, while the cohesion decreases with growth of the rock block proportion. However, all these three parameters increase as the rock block size (rock block proportion of 50 %) increases.     

The Linear Coregionalization Model and the Product–Sum Space–Time Variogram

The product covariance model, the product–sum covariance model, and the integrated product and integrated product–sum models have the advantage of being easily fitted by the use of marginal variograms. These models and the use of the marginals are described in a series of papers by De Iaco, Myers, and Posa. Such models allow not only estimating values at nondata locations but also prediction in future times, hence, they are useful for analyzing air pollution data, meteorological data, or ground water data. These three kinds of data are nearly always multivariate and because the processes determining the deposition or dynamics will affect all variates, a multivariate approach is desirable. It is shown that the use of marginal variograms for space–time modeling can be extended to the multivariate case and in particular to the use of the Linear Coregionalization Model (LCM) for cokriging in space–time. An application to an environmental data set is given.     

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.