Lithologic controls on mineralization at the Lagunas Norte high-sulfidation epithermal gold deposit, northern Peru

The 13.1-Moz high-sulfidation epithermal gold deposit of Lagunas Norte, Alto Chicama District, northern Peru, is hosted in weakly metamorphosed quartzites of the Upper Jurassic to Lower Cretaceous Chimú Formation and in overlying Miocene volcanic rocks of dacitic to rhyolitic composition. The Dafne and Josefa diatremes crosscut the quartzites and are interpreted to be sources of the pyroclastic volcanic rocks. Hydrothermal activity was centered on the diatremes and four hydrothermal stages have been defined, three of which introduced Au ± Ag mineralization. The first hydrothermal stage is restricted to the quartzites of the Chimú Formation and is characterized by silice parda, a tan-colored aggregate of quartz-auriferous pyrite–rutile ± digenite infilling fractures and faults, partially replacing silty beds and forming cement of small hydraulic breccia bodies. The δ³⁴S values for pyrite (1.7–2.2?‰) and digenite (2.1?‰) indicate a magmatic source for the sulfur. The second hydrothermal stage resulted in the emplacement of diatremes and the related volcanic rocks. The Dafne diatreme features a relatively impermeable core dominated by milled slate from the Chicama Formation, whereas the Josefa diatreme only contains Chimú Formation quartzite clasts. The third hydrothermal stage introduced the bulk of the mineralization and affected the volcanic rocks, the diatremes, and the Chimú Formation. In the volcanic rocks, classic high-sulfidation epithermal alteration zonation exhibiting vuggy quartz surrounded by a quartz–alunite and a quartz–alunite–kaolinite zone is observed. Company data suggest that gold is present in solid solution or micro inclusions in pyrite. In the quartzite, the alteration is subtle and is manifested by the presence of pyrophyllite or kaolinite in the silty beds, the former resulting from relatively high silica activities in the fluid. In the quartzite, gold mineralization is hosted in a fracture network filled with coarse alunite, auriferous pyrite, and enargite. Alteration and mineralization in the breccias were controlled by permeability, which depends on the type and composition of the matrix, cement, and clast abundance. Coarse alunite from the main mineralization stage in textural equilibrium with pyrite and enargite has δ³⁴S values of 24.8–29.4?‰ and $ {\delta^{18 }}{{\mathrm{O}}_{{\mathrm{S}{{\mathrm{O}}_4}}}} $ values of 6.8–13.9?‰, consistent with H₂S as the dominant sulfur species in the mostly magmatic fluid and constraining the fluid composition to low pH (0–2) and logfO₂ of ?28 to ?30. Alunite–pyrite sulfur isotope thermometry records temperatures of 190–260 °C; the highest temperatures corresponding to samples from near the diatremes. Alunite of the third hydrothermal stage has been dated by ⁴⁰Ar/³⁹Ar at 17.0?±?0.22 Ma. The fourth hydrothermal stage introduced only modest amounts of gold and is characterized by the presence of massive alunite–pyrite in fractures, whereas barite, drusy quartz, and native sulfur were deposited in the volcanic rocks. The $ {\delta^{18 }}{{\mathrm{O}}_{{\mathrm{S}{{\mathrm{O}}_4}}}} $ values of stage IV alunite vary between 11.5 and 11.7?‰ and indicate that the fluid was magmatic, an interpretation also supported by the isotopic composition of barite (δ³⁴S?=?27.1 to 33.8?‰ and $ {\delta^{18 }}{{\mathrm{O}}_{{\mathrm{S}{{\mathrm{O}}_4}}}} $ ?=?8.1 to 12.7?‰). The Δ³⁴S_py–alu isotope thermometry records temperatures of 210 to 280 °C with the highest values concentrated around the Josefa diatreme. The Lagunas Norte deposit was oxidized to a depth of about 80 m below the current surface making exploitation by heap leach methods viable.     

Genetic relations among basic lavas and ultramafic nodules: Evidence from oxygen isotope compositions

¹⁸O values of unaltered basic lavas range from 4.9 to 8.3 but different types of basalts are usually restricted to narrow and distinct ranges of isotopic composition. The average ¹⁸O values for Hawaiian tholeiites, mid-ocean ridge tholeiites, and alkali basalts are 5.4, 5.7, and 6.2 permil, respectively. Potassic lavas and andesites tend to be more ¹⁸O rich with ¹⁸O values between 6.0 and 8.0 permil. The differences among the oxygen isotopic compositions of most of these lavas can be attributed to partial melting of isotopically distinct sources. The oxygen isotope compositions of the sources may be a function of prior melting events which produce ¹⁸O-depleted partial melts and ¹⁸O-enriched residues as a consequence of relatively large isotopic fractionations that exist at high temperatures. It is proposed that lavas with relatively low ¹⁸O values are derived from primitive, ¹⁸O-depleted sources whereas ¹⁸O-rich basalts are produced from refractory sources that have already produced partial melts. High temperature fractionations among silicate liquids and coexisting minerals can be used in conjunction with the oxygen isotope compositions of ultramafic nodules to place constraints on the genetic relations between some nodules and different types of basic lavas.     

The La Unión Au ± Cu prospect,Camagüey District,Cuba: fluid inclusion and stable isotope evidence for ore-forming processes

The Camagüey district, Cuba, is known for its epithermal precious metal deposits in a Cretaceous volcanic arc setting. Recently, the La Unión prospect was discovered in the southern part of the district, containing gold and minor copper mineralization interpreted as porphyry type. Mineralization is hosted in a 73.0 ± 1.5 Ma calc–alkaline I-type oxidized porphyry quartz diorite intrusive within volcanic and volcaniclastic rocks of the early Cretaceous Guáimaro Formation. The porphyry is affected by propylitic alteration and crosscut by a network of quartz and carbonate veinlets and veins. Chlorite, epidote, sericite, quartz, and pyrite are the main minerals in the early veins which are cut by late carbonate and zeolite veins. Late barite pseudomorphously replaces pyrite. Gold is associated with pyrite as disseminations in the altered quartz diorite and in the veins, occurring as inclusions or filling fractures in pyrite with 4 g/t Au in bulk samples, and up to 900 ppm Au in in pyrite. Fluid inclusion and oxygen isotope data are consistent with a H₂O–NaCl–(KCl) mineralizing fluid, derived from the quartz diorite magma, and trapped at least at 425°C and 1.2 kbar. This primary fluid unmixed into two fluid phases, a hypersaline aqueous fluid and a low-salinity vapor-rich fluid. Boiling during cooling may have played an important role in metal precipitation. Pyrite δ³⁴S values for the La Unión prospect range between 0.71‰ and 1.31‰, consistent with a homogeneous magmatic sulfur source. The fluids in equilibrium with the mineralized rocks have estimated δ¹⁸O values from 8‰ to 11.8‰, calculated for a temperature range of 480–505°C. The tectonic environment of the La Unión prospect, its high gold and low copper contents, the physical–chemical characteristics of the mineralizing fluids and the isotopic signature of the alteration minerals and fluids indicate that the La Unión gold mineralization is similar to the porphyry gold type, even though the ore-related epidote–chlorite alteration can be classified as propylitic and not the classic potassic and/or phyllic alteration. The low copper contents in the prospect could be due to a mineralizing fluid previously saturated in copper, which is indicated by trapped chalcopyrite crystals in high-temperature fluid inclusions. The low-temperature paragenesis, represented by carbonate, zeolite and barite, indicates epithermal overprint. The study shows the potential for other gold porphyry-type deposits in the Cretaceous volcanoplutonic arc of Cuba.     

Evidence from mantle xenoliths for relatively thin (<100 km) continental lithosphere below the Phanerozoic crust of southernmost South America

Garnet peridotite xenoliths in the Quaternary Pali-Aike alkali olivine basalts of southernmost South America are samples of the deeper portion of continental lithosphere formed by accretion along the western margin of Gondwanaland during the Phanerozoic. Core compositions of minerals in garnet peridotites indicate temperatures of 970 to 1160°C between 1.9 and 2.4 GPa, constraining a geothermal gradient which suggests a lithospheric thickness of approximately 100 km below this region. Previously, this lithosphere may have been heated and thinned to ≤80 km during the Jurassic break-up of Gondwanaland, when widespread mafic and silicic volcanism occurred in association with extension in southern South America. Subsequent cooling, by up to >175°C, and thickening, by about 20 km, of the lithosphere is reflected in low-temperature (<970°C) spinel peridotites by chemical zonation of pyroxenes involving a rimward decrease in Ca, and in moderate- and high-temperature (>970°C) peridotites by textural evidence for the transformation of spinel to garnet. A recent heating event, which probably occurred in conjunction with modal metasomatism related to the genesis of the Pali-Aike alkali olivine basalts, has again thinned the lithosphere to <100 km. Evidence for this heating is preserved in moderate- and high-temperature (>970°C) peridotites as chemical zonation of pyroxenes involving a rimward increase in Ca, and by kelyphitic rims around garnet. The majority of moderate- and high-temperature (>970°C) xenoliths are petrochemically similar to the asthenospheric source of mid-oceanic ridge basalts: fertile (>20% modal clinopyroxene and garnet), Fe-rich garnet lherzolite with major element composition similar to estimates of primitive mantle, but large-ion-lithophile and light-rare-earth element depletion relative to heavy-rare-earth elements, and with Sr, Nd, Pb, Os, and O isotopic compositions similar to MORB. In contrast, infertile, Mg-rich spinel harzburgite is predominant among low-temperature (<970°C) xenoliths. This implies a significant chemical gradient and increasing density with depth in the mantle section represented by the xenoliths, and the absence of a deep, low density, olivine-rich root below the southernmost South American crust such as has been inferred below Archean cratons. With respect to both temperature/rheology and chemistry/density, the subcontinental mantle lithosphere below southernmost South America is similar to that below oceanic crust. It is interpreted to have formed by tectonic capture, during the Paleozoic, of a segment of what had previously been oceanic lithosphere generated at a late Proterozoic mid-oceanic spreading ridge.     

Advances in understanding the Kombolgie Subgroup and unconformity-related uranium deposits in the Alligator Rivers Uranium Field and how to explore for them using lithogeochemical principles

The Alligator Rivers Uranium Field (ARUF) includes the mined and unmined Jabiluka, Ranger, Koongarra and Nabarlek unconformity-related uranium deposits and several small prospects including the newly discovered King River prospect. Uranium mineralisation is hosted by a variety of metamorphosed Nimbuwah Domain lithologies that are unconformably overlain by the Kombolgie Subgroup, a basin package of unmetamorphosed arenites and mafic volcanics. All of the uranium deposits and prospects preserve an identical alteration assemblage that is subdivided into a distal and proximal alteration zone. The distal alteration zone comprises an assemblage of sericite and chlorite that replace albite and amphibole. In some cases, this alteration can be traced >1000 m from the proximal alteration zone that is dominated by uraninite, hematite, chlorite and sericite. Uranium precipitated in the basement as uraninite at 1680 Ma at around 200°C from a fluid having δ¹⁸O_fluid values of 3.0±2.8‰ and δD_fluid values of ?28±13‰ VSMOW reflecting an evolved marine source. These geochemical properties are indistinguishable from those recorded by diagenetic illite and chlorite that were collected from the Kombolgie Subgroup sandstones across the ARUF. The illite and chlorite formed in diagenetic aquifers, and where these aquifers intersected favourable basement rocks, such as those containing graphite or other reductants, U was precipitated as uraninite. Therefore, it is proposed that the Kombolgie Subgroup is the source for fluids that formed the deposits. A post-ore alteration assemblage dominated by chlorite, but also comprising quartz±dolomite±sulfide veins cut the uranium mineralisation at all deposits and has historically been recorded as part of the syn-ore mineralisation event. However, these minerals formed anywhere between 1500 to 630 Ma from fluids that have distinctly lower δ¹⁸O_fluid values around 1.5‰ and lower δD_fluid values around ?45‰ reflecting a meteoric water origin. Despite unconformity-related uranium deposits having a large alteration halo, they remain difficult to find. The subtle alteration of albite to sericite several hundred metres from mineralisation occurs in isolation of any increase in trace elements such as U and radiogenic Pb and can be difficult or impossible to identify in hand specimen. Whole rock geochemical data indicate that Pearce Element Ratio (PER) analysis and General Element Ratio (GER) analysis may vector into this subtle alteration because it does not rely on an increase in trace elements to identify proximity to ore. PER and GER plots, Al/Ti vs (2Ca + Na + K)/Ti, Na/Al vs (Na + K)/Al, K/Al vs (Na + K)/Al and (Fe + Mg)/Al vs (Na + K)/Al provide a visual guide that readily distinguish unaltered from altered samples. A plot of (Na + K)/Al and (Fe + Mg)/Al on the x-axis against the concentration of trace elements on the y-axis reveals that U, Pb, Mo, Cu, B, Br, Ce, Y, Li, Ni, V and Nd are associated with the most intensely altered samples. The lithogeochemical vectors should aid explorers searching for uranium mineralisation in a prospective basin environment, but exploration must first focus on the characteristics of the basin to assess its mineralisation potential. A holistic model that describes the evolution of the Kombolgie Subgroup from deposition through diagenesis to formation of the uranium deposits in the underlying basement rocks is presented and has application to other basins that are considered prospective for unconformity-related uranium deposits. The model outlines that explorers will need to consider the thickness of the sedimentary pile, its lithological composition relative to depositional setting, the depth to which the sediments were buried during diagenesis and the degree of diagenesis achieved, which may be time dependant, before deciding on the prospectivity of the basin.     

Constraints on the origin of alkaline and calc-alkaline magmas from the Tuxtla Volcanic Field,Veracruz, Mexico

 Lavas erupted in the Tuxtla Volcanic Field (TVF) over the last 7 Ma include primitive basanites and alkali basalts, mildly alkaline Hy-normative mugearites and benmoreites, and calc-alkaline basalts and basaltic andesites. The primitive lavas are silica-undersaturated, with high concentrations of both incompatible and compatible trace elements, variable La/Yb with constant Yb at 6 to 8 times chondritic, and low Sr and O and variable Pb and Nd isotopic ratios. The primitive magmas originated by increasing degrees of melting with pressure decreasing from greater than 30 kbar to 20 kbar, in the garnet stability field. Another group of alkali basalts and hawaiites has lower Ni and Cr concentrations and higher Fe/Mg ratios, and was derived from the primitive group by crystal fractionation at pressures of several kbar. Incompatible trace elements in these silica undersaturated lavas show depletion in high field strength elements (HFSE) relative to large ion lithophile elements, similar to subduction-related basalts. Ba/Nb ratios are nearly constant and thus the HFSE depletion cannot be the result of a residual HFSE-bearing phase in the source, but could be the result of generation from a source contaminated by fluids or melts from the subducted lithosphere. The silica-saturated mugearites and benmoreites, and the calc-alkaline basalts and basaltic andesites, were erupted only between 3.3 and 1.0 Ma. These have incompatible element concentrations generally lower than in the silica-undersaturated lavas, and thus could not have been derived by crystal fractionation from the silica-undersaturated alkaline magmas. Magmas parental to the silica-saturated magmas originated by higher degrees of melting at lower pressures than the primitive magmas. Melting may have been promoted by an influx of fluid from the subducted lithosphere. Trace element and Sr, Nd, Pb and O isotopic data suggest that three components are involved in the generation of TVF magmas: the mantle, a fluid from the subducted lithosphere, and continental crust. TVF alkaline lavas are similar to those erupted in the back-arc region of the MVB and Japan, and show characteristics similar to alkaline magmas erupted in the southern Andean volcanic arc. These low degree melts reach the surface along with calc-alkaline lavas in the TVF due to an extensional stress field that allows their passage to the surface. Received: 15 September 1994/Accepted: 14 February 1995     

An oxygen isotope study of two contrasting orogenic vein gold systems in the Meguma Terrane, Nova Scotia, Canada, with implications for fluid sources and genetic models

Sampling of quartz vein material from two gold deposits of similar geological setting but different ages (The Ovens, 408?Ma; Dufferin, 380?Ma) in the Meguma Terrane of Nova Scotia has been done to compare and contrast their ??¹⁸O_quartz signatures. Despite different ages of formation, quartz from all vein types in each of the deposits (i.e. saddle-reef, bedding-concordant leg reefs, en echelon, discordant) shows limited intra-deposit variation with similar average ??¹⁸O values of +15.2?±?0.9?? (n?=?16) for The Ovens and +15.7?±?0.6?? (n?=?12) for Dufferin. Using an average ??¹⁸O value of +15.4?? for the two deposits, the corresponding ??¹⁸O_H2O values, calculated for 400°C and 350°C based on constraints from mineral assemblages and fluid inclusion studies, indicate averages of 11.4?±?0.2?? and +10.2?±?0.2??, respectively. The isotopic data indicate that: (1) the vein-forming fluids have a metamorphic signature, (2) all vein types in the two deposits represent formation from a single, isotopically homogeneous fluid, and (3) a fluid of similar isotopic signature was generated by two contrasting tectono-thermal events in the Meguma Terrane that were separated by 30?Ma. Integration of these results with previously published data for 14 Meguma gold deposits indicate a general stratigaphic dependence in ??¹⁸O_H2O values for deposits when arranged in their relative stratigraphic position such that ??¹⁸O_H2O values increase upwards in the stratigraphy. This apparent trend cannot be explained by models involving either fluid mixing or cooling of the vein-forming fluids, but instead is modelled using fluid/rock interaction taking into account a change in the modal mineralogy of the metasedimentary rocks upwards in the stratigraphy.     

Hydrogen isotope systematics of submarine basalts

The D/H ratios and water contents in fresh submarine basalts from the Mid-Atlantic Ridge, the East Pacific Rise, and Hawaii indicate that the primary D/H ratios of many submarine lavas have been altered by processes including (1) outgassing, (2) addition of seawater at magmatic temperature, and (3) low-temperature hydration of glass. Decreases in δD and H²O⁺ from exteriors to interiors of pillows are explained by outgassing of water whereas inverse relations between δD and H₂O⁺ in basalts from the Galapagos Rise and the FAMOUS Area are attributed to outgassing of CH₄ and H₂. A good correlation between δD values and H₂O is observed in a suite of submarine tholeiites dredged from the Kilauea East Rift Zone where seawater (added directly to the magma), affected only the isotopic compositions of hydrogen and argon. Analyses of some glassy rims indicate that the outer millimeter of the glass can undergo lowtemperature hydration by hydroxyl groups having δD values as low as ?100.δD values vary with H₂O contents of subaerial transitional basalts from Molokai, Hawaii, and subaerial alkali basalts from the Society Islands, indicating that the primary δD values were similar to those of submarine lavas.Extrapolations to possible unaltered δD values and H₂O contents indicate that the primary δD values of most thoteiite and alkali basalts are near ?80 ± 5: the weight percentages of water are variable, 0.15–0.35 for MOR tholeiites, about 0.25 for Hawaiian tholeiites, and up to 1.1 for alkali basalts. The primary δD values of ?80 for most basalts are comparable to those measured for deep-seated phlogopites. These results indicate that hydrogen, in marked contrast to other elements such as Sr, Nd, Pb, and O, has a uniform isotopic composition in the mantle. This uniformity is best explained by the presence of a homogeneous reservoir of hydrogen that has existed in the mantle since the very early history of the Earth.     

A fluid inclusion and isotopic study of an intrusion-related gold deposit (IRGD) setting in the 380 Ma South Mountain Batholith,Nova Scotia,Canada: evidence for multiple fluid reservoirs

A set of sheeted quartz veins cutting 380 Ma monzogranite at Sandwich Point, Nova Scotia, Canada, provide an opportunity to address issues regarding fluid reservoirs and genesis of intrusion-related gold deposits. The quartz veins, locally with arsenopyrite (≤5%) and elevated Au–(Bi–Sb–Cu–Zn), occur within the reduced South Mountain Batholith, which also has other zones of anomalous gold enrichment. The host granite intruded (P = 3.5 kbars) Lower Paleozoic metaturbiditic rocks of the Meguma Supergroup, well known for orogenic vein gold mineralization. Relevant field observations include the following: (1) the granite contains pegmatite segregations and is cut by aplitic dykes and zones (≤1–2 m) of spaced fracture cleavage; (2) sheeted veins containing coarse, comb-textured quartz extend into a pegmatite zone; (3) arsenopyrite-bearing greisens dominated by F-rich muscovite occur adjacent the quartz veins; and (4) vein and greisen formation is consistent with Riedel shear geometry. Although these features suggest a magmatic origin for the vein-forming fluids, geochemical studies indicate a more complex origin. Vein quartz contains two types of aqueous fluid inclusion assemblages (FIA). Type 1 is a low-salinity (≤3 wt.% equivalent NaCl) with minor CO₂ (≤2 mol%) and has T _h = 280–340°C. In contrast, type 2 is a high-salinity (20–25 wt.% equivalent NaCl), Ca-rich fluid with T _h = 160–200°C. Pressure-corrected fluid inclusion data reflect expulsion of a magmatic fluid near the granite solidus (650°C) that cooled and mixed with a lower temperature (400°C), wall rock equilibrated, Ca-rich fluid. Evidence for fluid unmixing, an important process in some intrusion-related gold deposit settings, is lacking. Stable isotopic (O, D, S) analyses for quartz, muscovite and arsenopyrite samples from vein and greisens indicate the following: (1) δ¹⁸O_qtz = +11.7‰ to 17.8‰ and δ¹⁸O_musc = +10.7‰ to +11.2‰; (2) δD_musc = −44‰ to−54‰; and (3) δ³⁴S_aspy = +7.8‰ to +10.3‰. These data are interpreted, in conjunction with fluid inclusion data, to reflect contamination of a magmatic-derived fluid (d¹⁸O_H2O {\delta^{{{18}}}}{{\hbox{O}}_{{{{\rm{H}}_{{2}}}{\rm{O}}}}}  ≤ +10‰) by an external fluid (d¹⁸O_H2O {\delta^{{{18}}}}{{\hbox{O}}_{{{{\rm{H}}_{{2}}}{\rm{O}}}}}  ≥ +15‰), the latter having equilibrated with the surrounding metasedimentary rocks. The δ³⁴S data are inconsistent with a direct igneous source based on other studies for the host intrusion (d¹⁸O_H2O {\delta^{{{18}}}}{{\hbox{O}}_{{{{\rm{H}}_{{2}}}{\rm{O}}}}}  = +5‰) and are, instead, consistent with an external reservoir for sulphur based on δ³⁴S_H2S data for the surrounding metasedimentary rocks. Divergent fluid reservoirs are also supported by analyses of Pb isotopes for pegmatitic K-feldspar and vein arsenopyrite. Collectively the data indicate that the vein- and greisen-forming fluids had a complex origin and reflect both magmatic and non-magmatic reservoirs. Thus, although the geological setting suggests a magmatic origin, the geochemical data indicate involvement of multiple reservoirs. These results suggest multiple reservoirs for this intrusion-related gold deposit setting and caution against interpreting the genesis of intrusion-related gold deposit mineralization in somewhat analogous settings based on a limited geochemical data set.     

Global perturbation of the marine Ca isotopic composition in the aftermath of the Marinoan global glaciation

Ca isotopic compositions of Marinoan post-glacial carbonate successions in Brazil and NW Canada were measured. Both basal dolostones display δ^44/40Ca values between 1 and 0.7‰, overlying limestones show a negative Ca isotope excursion to values around 0.1‰, and δ^44/40Ca values rapidly increase up-section to near 2.0‰. In the Brazilian successions, those high δ^44/40Ca values rapidly decrease and stabilize to values between 0.6 and 0.9‰. These Ca isotope secular variation trends are unlike those of Sturtian post-glacial carbonate successions, but similar to those of Marinoan post-glacial carbonate successions in Namibia, suggesting that the perturbation of the marine Ca cycle was global. This recommends Ca isotope stratigraphy as a tool to correlate Neoproterozoic post-glacial carbonate successions worldwide.