Massive Sulfide Deposits Research Articles

PLATE TECTONICS AS A TOOL FOR GLOBAL SCREENING OF MAGMATIC ARCS AND PREDICTIONS FOR RELATED PORPHYRY DEPOSITS

Abstract The formation of most mineral deposits is closely linked to a geodynamic context—for example, the association of porphyry Cu-Au-Mo deposits with subduction and development of volcanic arcs. This paper proposes a new approach to the global screening of volcanic arcs and their duration, as a predictive method for a mineral systems-based approach (e.g., discovery of potential porphyry occurrences). The method utilizes geospatial and temporal analytics run on a combination of large global data sets and a global plate tectonic model (covering the time period 600 Ma to present) containing plate boundaries. The method involves (1) calculating present-day arc volcano-to-trench distances and obtaining average volcanic-arc widths in both continental and intraoceanic settings, (2) applying these values to the paleotrenches contained in the plate tectonic model on 53 time intervals spread throughout the Phanerozoic, (3) unreconstructing the results back to present day, and (4) summing up all magmatic arc occurrences using their cumulative durations. This results in a spatiotemporal model of the total cumulative duration of magmatic arc activity at the global scale, back to 600 Ma, that is updatable and can serve as a proxy to predict porphyry deposit likelihood. The model output is tested against a porphyry copper occurrence data set to validate the approach as a predictive proxy for arc-related porphyry deposits. The alignment of the model results with data control is high for most geologic time periods throughout the Phanerozoic—up to 90% in the case of buffered (1σ) magmatic arcs and up to 100% in the case of buffered magmatic arcs with an additional search distance (2σ). Recent advances in plate tectonic model quality and detail now offer a higher level of precision and confidence than ever before and enable tools for the prediction and screening of porphyry deposit locations, as well as opening the potential to screen for other geodynamic context-dependent commodities (e.g., orogenic gold, volcanogenic massive sulfide, or Ni and platinum group element-sulfide deposits), particularly in the search for poorly exposed or subsurface orebodies.

Acid Mine Drainage Effects in the Hydrobiology of Freshwater Streams from Three Mining Areas (SW Portugal): A Statistical Approach.

Aljustrel, Lousal and S. Domingos mines are located in the Iberian Pyrite Belt (IPB), one of the greatest massive sulfide ore deposits worldwide. These mines’ surrounding streams are affected by Acid Mine Drainage (AMD). The main purpose of this study was to understand AMD influence in the water quality and diatom behavior. Thus, waters and diatoms were sampled in 6 sites from the 3 selected mines on winter and summer of 2016. The highest concentrations were found in acidic sites: A3 (Aljustrel—Al, Cd, Cu, Fe and Zn (and lowest pH)) and L1 (Lousal—As, Mn, Ca, Mg, SO42− and conductivity). The most abundant diatom species was Pinnularia aljustrelica with 100% of dominance in A3 and S1 acidic sites, which puts in evidence this species adaptation to AMD harsh conditions. Multivariate cluster analysis allowed us to reinforce results from previous studies, where spatial differences were more relevant than seasonal ones. In 12 years (2004–2016), and with many transformations undertaken (re-opening and rehabilitation), there is a conservative behavior in the biological species (diatoms) and physicochemical concentrations (metals, pH and sulfates) from these three mining sites. This type of biogeochemical diagnosis is necessary for the sustainable use of these waters and the prevention of the polluting process, aimed to protect the water ecosystem and its biodiversity.

Iron isotopes constrain sub-seafloor hydrothermal processes at the Trans-Atlantic Geotraverse (TAG) active sulfide mound

Sub-seafloor hydrothermal processes along volcanically active plate boundaries are integral to the formation of seafloor massive sulfide deposits and to oceanic iron cycling, yet the nature of their relationship is poorly understood. Here we apply iron isotope analysis to sulfide minerals from the Trans-Atlantic Geotraverse (TAG) mound and underlying stockwork, 26°N Mid-Atlantic Ridge, to trace hydrothermal processes inside an actively-forming sulfide deposit in a sediment-free mid-ocean ridge setting. We show that data for recently formed chalcopyrite imply hydrothermal fluid–mound interactions cause small negative shifts (<−0.1‰) to the δ56Fe signature of dissolved iron released from TAG into the North Atlantic Ocean. Texturally distinct types of pyrite, in turn, preserve a δ56Fe range from −1.27 to +0.56‰ that reflects contrasting precipitation mechanisms (hydrothermal fluid–seawater mixing vs. conductive cooling) and variable degrees of progressive hydrothermal maturation during the >20 kyr evolution of the TAG complex. The identified processes may explain iron isotope variations found in fossil onshore sulfide deposits.

Ultramafic-hosted volcanogenic massive sulfide deposits from Cuban ophiolites

Ultramafic-hosted volcanogenic massive sulfide deposits (UM-VMS) located in the Havana-Matanzas ophiolite (Cuba) are the only known example of this type of mineralization in the Caribbean realm. UM-VMS from Havana-Matanzas are enriched in Cu, Ni, Co, Au, and Ag. The mineralization consists of massive sulfide bodies mostly composed of pyrrhotite and hosted by serpentinized upper mantle peridotites. Chemical composition of unaltered cores in Cr-spinel grains found within the massive sulfide mineralization and in the peridotite host indicates formation in the fore-arc region of the Greater Antilles volcanic arc. A first stage of serpentinization probably took place prior to the sulfide mineralization event. The UM-VMS mineralization formed by the near-complete replacement of the silicate assemblage of partially serpentinized peridotites underneath the seafloor. The sequence of sulfide mineralization has been divided into two stages. The first stage is characterized by a very reduced hydrothermal mineral assemblage consisting of pyrrhotite, Co–Ni–Fe diarsenides, chalcopyrite, Co-rich pentlandite, and electrum. In the second stage, pyrite and Co–Ni–Fe sulfarsenides partially replaced pyrrhotite and diarsenides, respectively, under a more oxidizing regime during the advanced stages of ongoing serpentinization. The proposed conceptual genetic model presented here can be useful for future exploration targeting this type of deposit in the Caribbean region and elsewhere.

A mineralogical and geochemical application for determining hydrothermal alteration zones associated with volcanic-hosted massive sulphide deposits at Tasik Chini area, Peninsular Malaysia

The volcanic-hosted massive sulphide (VHMS) deposits of the Tasik Chini area, Peninsular Malaysia are hosted by Permian felsic volcanic rocks (∼ 290 Ma) of rhyolitic to rhyodacitic composition and comprise two deposits (Bukit Botol and Bukit Ketaya). Although the ores and the felsic volcanic host rocks of these deposits have metamorphosed to greenschist facies and were affected by a complex deformation history, the hydrothermal alteration zones associated with mineralization are preserved and show systematic mineralogical and geochemical changes with increasing proximity to the ore bodies. The geometry of alteration assemblages of the Bukit Botol and Bukit Ketaya deposits shows they occur as semi-conformable or stratabound zones around the ore lenses. According to petrography study and short wavelength infrared (SWIR) spectra measurements supported by X-Ray diffractometer (XRD), the Bukit Botol deposit is characterised by proximal quartz-sericite-pyrite and distal quartz-sericite alteration zones, whereas distal quartz-chlorite-sericite-pyrite-pyrophyllite ± kaolinite and proximal quartz-chlorite-pyrite ± carbonate ± pyrophyllite form the alteration assemblages of the Bukit Ketaya deposit. The geochemical data is coherent with the mineralogical characteristics, using the Ishikawa alteration (AI) and chlorite-carbonate-pyrite (CCPI) indexes, showing the important of chlorite and sericite formation in the ore proximal and ore distal zones. In addition, the molar elemental ratios of Na2O/Al2O3 versus K2O/Al2O3 and MgO/Al2O3 versus K2O/Al2O3 support that the abundance of muscovite (sericite) and chlorite controlled the intensity of alteration at the both deposits. The results of this study indicate that the combination of mineralogy and geochemistry studies help in defining specific alteration styles and related mineral geochemical variations of the VHMS deposits in Tasik Chini area.

High-Precision CA-ID-TIMS U-Pb Zircon Geochronology of Felsic Rocks in the Finlayson Lake VMS District, Yukon: Linking Paleozoic Basin-Scale Accumulation Rates to the Occurrence of Subseafloor Replacement-Style Mineralization

Abstract Felsic igneous complexes and associated volcano-sedimentary rocks in continental back-arc environments host large-tonnage and/or high-grade volcanogenic massive sulfide (VMS) deposits. The emplacement mechanisms, style, and preservation of these deposits is thought to be partially dependent on depositional rates of the host lithofacies (i.e., discrete volcanic eruptions) relative to the setting of massive sulfide genesis on the seafloor as mounds and/or via subseafloor replacement of existing strata. The localization and occurrence of subseafloor replacement-style VMS deposits is therefore strongly influenced by the characteristics of the volcano-sedimentary facies in the hosting basin and the rates of their emplacement; the latter are poorly constrained in the literature due to the difficulty of obtaining high-precision dates that make this possible in Phanerozoic and older rocks. New high-resolution U-Pb geochronology and detailed regional stratigraphic investigation indicate that Devonian-Mississippian volcanic rocks and associated VMS mineralization in the Yukon-Tanana terrane in the Finlayson Lake district, Yukon, Canada, were erupted or emplaced during distinct time periods (ca. 363.3, 362.8, and 355.2 Ma) in two discrete submarine basins: the Kudz Ze Kayah formation and the Wolverine Lake group. The VMS deposits in both settings are contained within intrabasinal rocks that accumulated at rapid rates of ~350 to 2,000 m/m.y. over 0.6 to 1.4 m.y. Locally, these rates reach peak rates up to 7,500 m/m.y. in the Wolverine Lake group, which are interpreted to reflect facies deposition by mass transport complexes or turbidity currents. These new dates indicate that rapid accumulation of volcanic rocks in the back-arc basins was critical for localizing subseafloor replacement-style mineralization and the development of the Zn-enriched GP4F, Kudz Ze Kayah, and Wolverine VMS deposits. Rapid depositional processes observed in these deposits and their host basins are interpreted to have an important role in developing highly porous and permeable, water-saturated lithofacies that provide optimal conditions for enhancing zone refining processes and subsequent preservation of massive sulfide mineralization, which are key in the development of high-grade and large-tonnage VMS deposits. It is herein suggested that quantitative basin-scale accumulation rates, as a result of new U-Pb geochronological methods and increased precision combined with detailed stratigraphic and facies analysis, may provide important perspectives on the formation of continental back-arc basins and the localization of VMS deposits in other continental margin environments globally.

Geology, Geochemistry, and Geochronology of the Giant Rio Tinto VMS Deposit, Iberian Pyrite Belt, Spain

Abstract The Rio Tinto deposit is a giant volcanogenic massive sulfide deposit (VMS) that contains more than 500 Mt of pyrite-rich massive sulfides and more than 2 Gt of mineralized stockwork. Three broad lithostratigraphic groups occur in the regional stratigraphy: the phyllite-quartzite group, the volcano-sedimentary complex, and the Baixo Alentejo Flysch Group. These three major packages reflect the evolution of a depositional environment from a stable platform to deposition in pull-apart continental basins during oblique subduction and collision and coeval synorogenic flysch sequence. The volcano-sedimentary complex, which hosts massive sulfide mineralization at Rio Tinto, can be divided into four major units: (1) the Mafic Siliciclastic Unit, (2) the Lower Sedimentary Unit, (3) the Felsic Unit, and (4) the Upper Sedimentary Unit. The Felsic Unit is further subdivided based on new U-Pb zircon geochronology into three distinct subunits. Felsic Unit I (ca. 356 Ma) includes dome complexes dominated by rhyodacite and reflects the onset of felsic magmatism in the region. Felsic Unit II (ca. 352–348 Ma) represents the main interval of volcanic activity, also dominated by rhyodacite domes and related aprons, and is associated with widespread VMS mineralization. Felsic Unit III (ca. 340 Ma) reflects a late pulse of rhyolitic volcanism. Massive sulfides occur as two different styles of mineralization: (1) replacive ores as discordant pipes hosted by glass-rich felsic rocks and enclosed by a large zone of stockwork-like mineralization and (2) overlying shale-hosted exhalative mineralization in small anoxic basins, probably formed during the collapse of the volcanic domes of Felsic Unit II in the Middle-Late Tournaisian. New lithogeochemical data illustrate two types of mafic rocks in the Mafic Siliciclastic Unit: a basaltic andesite and a high–Ti-Zr basalt, both of tholeiitic affinity. Using immobile element ratios (heavy rare earth elements [HREEs], Al, Y, Zr, and Ti) of the Felsic Unit, fundamental differences have been recognized between the subunits. The unmineralized Felsic Unit I is characterized by high Zr content (225–300 ppm) and a pronounced Eu negative anomaly, and probably represents the most fractionated rocks. Felsic Unit II is characterized by Zr values between 50 and 200 ppm. The low Zr values of the mineralized unit contrast with the typically high Zr values of the felsic rocks related to volcanogenic massive sulfides elsewhere and, at a regional scale, can help to discriminate potentially fertile domes from barren volcanism.

Petrochemical evaluation of gahnite from volcanogenic massive sulfide deposits in Betul belt, Central India: Insight from petrography and in‐situ trace element geochemistry

Gahnite occurs in diverse rock types and metamorphosed mineral deposits. The gahnite geochemistry is being used as an exploration tool for zinc sulfide deposits. In the present study, the geochemistry of gahnite and associated minerals viz. sphalerite, garnet, sillimanite, staurolite, anthophyllite, biotite, ilmenite, and chlorite, and their petrography have been used in studying the genesis, metamorphic evolution, deposit characterization, and exploration significance of seven Palaeoproterozoic volcanogenic massive sulfides (VMS) deposits in the Betul belt in the Central Indian Tectonic Zone, India. Different textural types of gahnites are recognized in the Betul belt. Field investigations of textural and geochemical characteristics suggest that the gahnites were formed by multiple geological processes: desulfidation of sphalerite, breakdown of almandine garnet, and zincian staurolite, and chloritization of zincian biotite corresponding with regional metamorphism. The temperature conditions of gahnite formation are estimated to be ~600–650°C using empirical Ti in biotite thermometry. The elemental concentrations in gahnites vary from Zn/Fe ratio 2–4; Co 1–30 ppm; Ga 14–573 ppm and Mn 126–3422 ppm, indicating that bimodal volcanics and volcano‐sedimentary rocks as protolith. High Mn content in gahnite suggests an influx of magmatic‐hydrothermal fluid in the protolith. Variations of trace elements (Mg vs. Al/V, Ti vs. Co/Mn, Co vs. V/Ga, Mn vs. Zn/Fe) and high‐temperature of gahnite formation attest to sensu stricto VMS type mineralization in Betul belt, which is entirely different from SEDEX, Broken Hill‐type, and non‐sulfide deposits. Principal component analysis of trace elements shows the geochemical variations at a few deposits and reveals that gahnites were formed as a result of the competing effect of fS2‐fO2 and governed by bulk rock composition.

Depth Profiles of Re-Os Geochemistry in Drill Cores from Hole U1530A in Brothers Volcano Hydrothermal Field, Kermadec Arc: Mobilization and Extreme Enrichment of Os by Volcanic Gas

AbstractBetter understanding metallogenesis in oceanic crust depends on costly sea-floor drilling projects in areas where metal-bearing deposits, such as sea-floor massive sulfide deposits, are currently forming. In 2018, International Ocean Discovery Program (IODP) Expedition 376 recovered drill cores from an active hydrothermal field at Brothers volcano, in the Kermadec arc. These provide insight into the formation of mineral deposits along arcs, the structure and permeability of hydrothermal sites, and the relationship between the discharge of magmatic fluids and the deep biosphere. We report whole-rock major and trace element compositions and the Re-Os isotope geochemistry of hydrothermally altered volcanic rocks in a core from Hole U1530A, extending 453 m beneath the sea floor, and unaltered volcanic rocks in cores from four other drilling sites and interpret these data to better understand subseafloor mixing of hydrothermal fluids and ambient seawater. The core exhibits more radiogenic 187Os/188Os values than typical basal values in four intervals. We propose two causal mechanisms of these radiogenic values: (1) mixing between seawater and hydrothermal fluid, associated with abundant deposition of sulfide or sulfate minerals; and (2) ingress of seawater with radiogenic 187Os/188Os values, associated with abundant chlorite and high porosity. Extreme Os enrichments up to 61.5 ppb are interpreted as the result of mobilization of Os as OsO4 or OsF6 and transport by volcanic gas, which also affected the Re-Os geochemistry of the rocks from the other Expedition 376 holes. Mobilization and transport of Os by volcanic gas may be an appreciable factor in the influx of unradiogenic Os into the ocean.

Age and Chemostratigraphy of the Finlayson Lake District, Yukon: Implications for Volcanogenic Massive Sulfide (VMS) Mineralization and Tectonics along the Western Laurentian Continental Margin

Abstract The Yukon-Tanana terrane in the Finlayson Lake district, Yukon, represents one of the first arc–back-arc systems that formed adjacent to the Laurentian continental margin in the mid-Paleozoic. Back-arc rocks contain many large and high-grade volcanogenic massive sulfide (VMS) deposits. This study integrates U-Pb zircon geochronology, lithogeochemistry, and Hf-Nd isotopes to establish precise controls on tectonomagmatic activity adjacent to the western Laurentian margin in the Late Devonian to Early Mississippian. High-precision chemical abrasion- (CA-) ID-TIMS U-Pb zircon geochronology defines coeval arc (ca. 363.1 to 348 Ma) and back-arc (ca. 363.3 to 355.0 Ma) magmatism in the Finlayson Lake district that intruded continental crust of Laurentian affinity (e.g., Snowcap assemblage). Mafic and felsic rocks display geochemical and isotopic characteristics that are consistent with being formed from mixtures of depleted asthenosphere and enriched lithospheric mantle sources. These melts variably entrained Laurentian continental crust via high-temperature crustal melting due to basaltic underplating. The high-temperature back-arc felsic magmatism occurs at specific time periods coinciding with VMS deposits and supports previous genetic models for VMS mineralization that suggest elevated heat flow and hydrothermal circulation were due to regional-scale rift-related magmatism rather than from local subvolcanic intrusions. The short timescales and transient nature of tectonomagmatic events in the Finlayson Lake district suggest that rapid and complex subduction initiation of oceanic and continental crust fragments facilitated coeval compression, extension, and magmatism in the arc and back-arc regions. We thus reevaluate the presently accepted tectonostratigraphic framework of the Finlayson Lake district and suggest revised interpretations that shed light on VMS depositional environments and a possible broader association with the ca. 358 Ma Antler Orogeny. Results of this study have implications for incipient tectonics, magmatism, and mineralization along the western Laurentian continental margin and other orogenic belts globally.

3D Constrained Gravity Inversion and TEM, Seismic Reflection and Drill-Hole Analysis for New Target Generation in the Neves–Corvo VMS Mine Region, Iberian Pyrite Belt

Located in the Iberian pyrite belt, the Neves–Corvo mine is a world-class massive sulfide deposit and the largest operating mine in Portugal with underground mining down to 1000 m depth focused on massive and stockwork Cu, Zn, Pb rich ores. Gravimetric data have had a leading role in the discovery of the seven known deposits, together with time-domain electromagnetic (TEM) ground data. In this work, we present the results of a 3D constrained gravity inversion carried out with legacy ground gravity data. The 3D gravity inversions were carried out using an updated density database containing approximately 142,000 measurements. A recently constructed 3D geological model based on reprocessed 2D seismic reflection, 3D seismic, TEM and updated geology from detailed surface mapping and drill-hole data, was used to constrain the inversions. The results show multiple high-density anomalies that may indicate the presence of mineralization at depth. These anomalies were therefore cross-checked with holes previously drilled. Approximately 97% of more than 1000 available surface drill-holes located on or at a distance of less than 200 m from the high-density anomalies intersected mineralization. However, gravity anomalies have been drilled in the past and particularly dense black shales or rhyolitic/gabbroic rocks have been intersected. To increase the success of future drilling, gravimetric anomalies have been correlated spatially with high-conductivity TEM zones and strong-amplitude seismic reflections, because igneous rocks usually present weak-to-moderate conductivity and a massive column of black shales presents a seismic signature quite different from that of mineralization. We concluded that some of these locations represent high-quality targets to consider following up with drilling and further exploration.

3D self-potential tomography of seafloor massive sulfide deposits using an autonomous underwater vehicle

Seafloor massive sulfide (SMS) deposits contain abundant metals, such as Cu, Zn, Au, and Ag, which are of growing economic interest. Currently, the exploration of SMS deposits has entered into a new stage of resource assessment, so we need a geophysical method to rapidly obtain the 3D structure of these SMS deposits. We report here a self-potential (SP) survey performed with an autonomous underwater vehicle (AUV) at the Yuhuang hydrothermal field on the ultraslow-spreading Southwest Indian Ridge with a water depth ranging from 1300 m to 2200 m. The electric-field sensors are attached to the tail of the AUV to record the electric field approximately 50 m above the seafloor. The electric field strength is observed to reach an amplitude of 0.6 mV/m at this known SMS deposit. SP tomography is used to obtain the 3D structure of the ore body, and benchmark numerical tests are first performed on synthetic cases to optimize the inversion algorithm parameters to estimate the ore location. The 3D SP tomography reveals a south-sloping ore body, which is 100 m long in the north–south direction and nearly 200 m long in the east–west direction. The vertical extent of the ore body is approximately 100 m. These results suggest that an AUV-based SP survey and tomography are potentially useful exploration methods to characterize the geometry of SMS deposits. This method may play an important role in resource assessment in concert with other geophysical methods, such as magnetic and induced-polarization surveys.

Automated Multi-Scale and Multivariate Geological Logging from Drill-Core Hyperspectral Data

Hyperspectral drill-core scanning adds value to exploration campaigns by providing continuous, high-resolution mineralogical data over the length of entire boreholes. However, multivariate mineralogical data must be transformed into lithological domains such that it is compatible with interpolation techniques and be usable for geomodeling. Manual interpretation of multivariate drill-core data is a challenging, time-consuming and subjective task, and automated or semi-automated approaches are needed. However, naive machine-learning techniques that ignore the distinct spatial structure and multi-scale nature of geological systems tend to produce geologically unreasonable results. Automated geological logging and multi-scale hierarchical domaining of drill-cores has been previously addressed in several studies by means of scalograms from a wavelet transform and tessellation, albeit exploiting only univariate information. The methodology involves the extraction of the local first principal component at a neighborhood of each observation, and the segmentation of the resulting series of scores with a continuous wavelet transform for boundary detection. In this way, the correlation pattern between the variables is incorporated into the segmentation. The scalogram accurately locates the geological boundaries at depth and yields hierarchical geological domains with mineralogical composition characteristics. The performance of this approach is demonstrated on a synthetic as well as a real multivariate dataset. The real dataset consists of mineral abundances derived from drill-core hyperspectral imaging data acquired in Elvira, a shale-hosted volcanogenic massive sulfide deposit located in the Iberian Pyrite Belt, where 7000 m of drill-core were acquired along 80 boreholes. The extracted domains are sensible from a geological point of view and spatially coherent across the boreholes in cross-sections. The results at relevant scales were qualitatively validated by comparing against the lithological log. This method is fast, is appropriate for multivariate geological data along boreholes, and provides a choice of scales for hierarchical geological domains along boreholes with mineralogical composition characteristics that can be modeled in 3D. Our approach provides an automatic way to transform hyperspectral image-derived mineral maps into vertically coherent geological units that are appropriate inputs for 3D geological modeling workflows. Moreover, the method improves the boundary detection and geological domaining by making use of multivariate information.

Vectors to ore in replacive volcanogenic massive sulphide deposits of the northern Iberian Pyrite Belt: Major and trace element mineral chemistry

As part of a broader characterization and study of vectors to ore in VMS systems of the Iberian Pyrite Belt (IPB, Spain), we have investigated in detail mineral chemistry vectors in a representative replacive deposit hosted in felsic volcanic rocks. At the Aguas Teñidas deposit (northern IPB) the hydrothermal system affected rocks of an originally homogeneous composition extending hundreds of metres beyond its footprint. The major and trace element chemistry of white micas, chlorite and carbonates have been analysed by electron microprobe (EMP) and laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) to characterize geochemical vectors across the extent of the hydrothermal system at Aguas Teñidas.White micas are dominated by muscovite in both regionally altered lithologies and within the hydrothermal system, with coexisting paragonite occurring in a halo beyond the first disseminated pyrite surrounding the stockwork and in the proximal hanging wall. Systematic variations have been observed in FeO/(FeO + MgO) and Na2O/(Na2O + K2O) across the alteration zone.Chlorite is predominantly clinochlore in composition, with chamosite restricted to the centre of the hydrothermal system. In regionally altered lithologied it is characterized by a constantly low Al and AlIV at variable Fe/(Fe + Mg); in rocks influenced by the hydrothermal system it presents higher AlIV and total Al, and a progressive increase in Al, AlIV and Fe/(Fe + Mg) towards its core.Regional carbonates consist of calcite, with additional dolomite forming in proximal rocks. Iron content in dolomite increases towards the centre of the hydrothermal system, with ankeritic compositions becoming dominant.Systematic variations in Ba, Cs, Li, Pb, Rb, Sn, Sr, Tl and Zn have been observed in white micas consistent with a proximal-distal transition (vector). Trends in chlorite have been less well characterized due to analytical limitations, although variations have been observed in the contents of As, Co, Li and Zn.A schematic model has been proposed which accounts for the observed mineralogical and mineral chemistry trends across the hydrothermal footprint of the Aguas Teñidas VMS deposit. Major element signatures in white micas and chlorite are interpreted as having been controlled by the upwards and outwards flow of hot reducing Fe-rich hydrothermal fluids producing a coupled increase in temperature and fluid Fe/(Fe + Mg), and a decrease in fO2, with increasing fluid/rock ratios towards the centre of the stockwork.The data presented herein are not only applicable to VMS exploration in the IPB, but on a broader scale improve our general understanding of vectors to ore in VMS deposits in general.

Lithospheric conductors reveal source regions of convergent margin mineral systems

The clean energy transition will require a vast increase in metal supply, yet new mineral deposit discoveries are declining, due in part to challenges associated with exploring under sedimentary and volcanic cover. Recently, several case studies have demonstrated links between lithospheric electrical conductors imaged using magnetotelluric (MT) data and mineral deposits, notably Iron Oxide Copper Gold (IOCG). Adoption of MT methods for exploration is therefore growing but the general applicability and relationship with many other deposit types remains untested. Here, we compile a global inventory of MT resistivity models from Australia, North and South America, and China and undertake the first quantitative assessment of the spatial association between conductors and three mineral deposit types commonly formed in convergent margin settings. We find that deposits formed early in an orogenic cycle such as volcanic hosted massive sulfide (VHMS) and copper porphyry deposits show weak to moderate correlations with conductors in the upper mantle. In contrast, deposits formed later in an orogenic cycle, such as orogenic gold, show strong correlations with mid-crustal conductors. These variations in resistivity response likely reflect mineralogical differences in the metal source regions of these mineral systems and suggest a metamorphic-fluid source for orogenic gold is significant. Our results indicate the resistivity structure of mineralized convergent margins strongly reflects late-stage processes and can be preserved for hundreds of millions of years. Discerning use of MT is therefore a powerful tool for mineral exploration.

Integrating Multidisciplinary Observations in Vent Environments (IMOVE): Decadal Progress in Deep-Sea Observatories at Hydrothermal Vents

The unique ecosystems and biodiversity associated with mid-ocean ridge (MOR) hydrothermal vent systems contrast sharply with surrounding deep-sea habitats, however both may be increasingly threatened by anthropogenic activity (e.g., mining activities at massive sulphide deposits). Climate change can alter the deep-sea through increased bottom temperatures, loss of oxygen, and modifications to deep water circulation. Despite the potential of these profound impacts, the mechanisms enabling these systems and their ecosystems to persist, function and respond to oceanic, crustal, and anthropogenic forces remain poorly understood. This is due primarily to technological challenges and difficulties in accessing, observing and monitoring the deep-sea. In this context, the development of deep-sea observatories in the 2000s focused on understanding the coupling between sub-surface flow and oceanic and crustal conditions, and how they influence biological processes. Deep-sea observatories provide long-term, multidisciplinary time-series data comprising repeated observations and sampling at temporal resolutions from seconds to decades, through a combination of cabled, wireless, remotely controlled, and autonomous measurement systems. The three existing vent observatories are located on the Juan de Fuca and Mid-Atlantic Ridges (Ocean Observing Initiative, Ocean Networks Canada and the European Multidisciplinary Seafloor and water column Observatory). These observatories promote stewardship by defining effective environmental monitoring including characterizing biological and environmental baseline states, discriminating changes from natural variations versus those from anthropogenic activities, and assessing degradation, resilience and recovery after disturbance. This highlights the potential of observatories as valuable tools for environmental impact assessment (EIA) in the context of climate change and other anthropogenic activities, primarily ocean mining. This paper provides a synthesis on scientific advancements enabled by the three observatories this last decade, and recommendations to support future studies through international collaboration and coordination. The proposed recommendations include: i) establishing common global scientific questions and identification of Essential Ocean Variables (EOVs) specific to MORs, ii) guidance towards the effective use of observatories to support and inform policies that can impact society, iii) strategies for observatory infrastructure development that will help standardize sensors, data formats and capabilities, and iv) future technology needs and common sampling approaches to answer today’s most urgent and timely questions.

Exploration for Byproduct Critical Element Resources: Proxy Development Using a LA–ICP–MS Database

The transition towards zero-CO2 energy generation, storage and transport will require a range of metals that are often considered critical and are produced as byproducts of the production of other metals. This means that the reliance of some critical elements on the production of main metal commodities, such as Cu and Ni, is a significant source of supply risk. However, how can we evaluate resource scarcity and supply risks for elements that we do not routinely analyze for and characterize in present day mined ores? Here we demonstrate a method for exploring for and assessing the byproduct critical element potential of magmatic sulfide and volcanogenic massive sulfide deposits using a LA–ICP–MS database. Our results indicate there are significant enrichments of Sb, Bi, Cd, Co, Se and Te in pentlandite (Ni sulfide), chalcopyrite (Cu sulfide) and sphalerite (Zn sulfide) within these systems, demonstrating the need for a holistic approach to critical element research with unrecovered byproducts in existing mining supply chains having the potential to solve perceived resource scarcity challenges.

Rock Magnetic Signatures of Hydrothermal Mineralization in the Trans‐Atlantic Geotraverse (TAG) Hydrothermal Field

AbstractThe Ocean Drilling Program Leg 158 drill holes from the Trans‐Atlantic Geotraverse hydrothermal field are investigated to understand the rock magnetic signatures of hydrothermal mineralization. A composite columnar section has been constructed through hole correlation to understand the stratigraphic variation of magnetomineralogy within the stockwork. Isothermal remanent magnetization components unmixing, first‐order reversal curve diagrams, low‐temperature magnetic signatures, and electron microscopic analyses disclose magnetic minerals of disparate occurrences related to predominating hydrothermal mineralization reactions in three broad zones: For basaltic basements, serpentinization of olivine phenocrysts during preliminary hydrothermal alteration produces magnetite, in addition to primary titanomagnetite; Chloritized and silicified zone samples contain relict titanomagnetite and exsolved magnetite that survived hydrothermal dissolution; Anhydrite and sulfide zone samples are dominated by magnetite and hematite, likely from oxidation of polymetallic sulfides due to exposure in oxidative seafloor environments during drilling. Our findings suggest that seafloor oxidation potentially modifies the magnetic properties of polymetallic sulfides in hydrothermal deposits, which applies to magnetic tomography of sophisticated subseafloor vent structures and prospecting seafloor massive sulfides (SMS) deposits therein. Meanwhile, we alert future deep‐sea mining that drilling may promote physicochemical alteration of SMS deposits, causing environmental risks. The established magnetic signatures ultimately contribute to understanding the in situ geological preservation of SMS deposits and optimizing exploitation procedures in the future.

Diagenesis of clastic ores of the Ishkininо Co-bearing massive sulfide deposit (Southern Urals): Mineralogical-geochemical data and thermodynamic modeling

Research subject. The transformed clastic ores (ore diagenites) of the Ishkinino Co-bearing massive sulfide deposit hosted by serpentinites of the Main Uralian Fault Zone.Materials and methods. The structures and textures of the ores were stu died. The trace element contents of sulfides and oxides were determined using LA ICP MS. The physical and chemical modeling of the diagenetic formation of accessory As minerals was conducted using the Selektor program package. Results. The clastic ores are transformed gravelites with angular and rounded clasts of serpentinites, sulfides and chromite in the psammitic matrix of the same mineral composition. No hydrothermal minerals remain in gravelites; they are replaced by crystalline pyrite-2, porous pyrite-3, anhedral pyrite-4, pyrrhotite, chalcopyrite and magnetite. Chalcopyrite and magnetite replace all sulfides, sulfarsenides, chromite and gangue minerals. Chromite occurs as fragmented crystals or inclusions into serpentinite clasts. The matrix hosts euhedral cobaltite crystals with nickeline, gersdorffite and native gold inclusions. Crystalline pyrite-2 is characterized by higher Mn, Co, Ni, Cu and Zn contents. Porous pyrite-3 exhibits higher Co, Cu and Se contents. Anhedral pyrite-4 is enriched in most trace element contents in comparison with other sulfides and pyrite generations. Chalcopyrite is characterized by higher contents of Zn and Se. Pyrrhotite contains the highest Ni and hi gher Co contents.Conclusions. The main trace elements in the ores of the deposit (Co and Ni), as well as Cu, Zn and Mn, are hosted not only in sulfides, but also in oxides. Thus, chromite contains Zn and Ni, while magnetite contains Mn and Cu. Selenium occurs in all sulfides in similar quantities. Tellurium is mostly concentrated in pyrite-4. A comparative analysis of our results with those reported on other massive sulfide deposits showed that the serpentinite-sulfide gravelites of the Ishkinino deposit had been intensely transformed during diagenesis, which resulted in low trace element contents in diagenetic sulfides. The diagenetic alteration of clastic ores led to the formation of authigenic cobaltite, gersdorffite, nickeline and native gold as a result of trace element release from primary hydrothermal minerals. Thermodynamic mode ling showed the possibility of formation of As-bearing minerals (in particular, nickeline) at temperatures of 200°C and below.

Recognizing the evolution of the stratabound polymetallic massive sulfide deposits in Tongling mineralization cluster, east China through colloform pyrite

Stratabound Cu-Au sulfide deposits are widely distributed in the Middle -Lower Yangtze River Mineralization Belt, eastern China. These deposits are strictly distributed along the Carboniferous stratum, but occur in close proximity to the Cretaceous diorite rocks. The simultaneous presence of sedimentary and magmatic evidence leads the genesis of these stratabound massive sulfide deposits to be an open question. Colloform pyrite (Py-c) is widely distributed in stratabound sulfide deposits and its genesis remains controversial which contrarily limits the establishment of a metallogenic model for the stratabound sulfide deposits. In this study, the mineral composition, morphology, microstructure, and organic composition of Py-c were systematically studied using optical microscopy, powder X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), micro-area laser Raman spectroscopy, and gas chromatography-mass spectrometry (GC–MS). Results reveal three types of textures of Py-c: oolitic, concentric-banded, and micritic (no other characteristic texture). The concentric-banded texture shows alternating light and dark bands which are composed of fine and coarse Py-c grains, respectively. All the Py-c ores are similar in phase composition, where the main phase is pyrite, the minor phases are siderite, dolomite, and quartz, and the trace phases are clay minerals (e.g., illite) and organic matter. The size of pyrite crystals varies from 50 nm to 1.4 μm. Most of the pyrite crystals are euhedral and subhedral, where the euhedral crystals show cubic and spheroidic shapes. The surfaces of cubic crystals are smooth and stripless. Detrital and authigenic quartz are found in Py-c ores. Detrital quartz grains are highly round. Py-c mold impressions are widespread on the grain surface. Py-c around the detrital quartz did not recrystallize. Authigenic quartz grains are euhedral and subhedral, cover a size range of hundreds of nanometers to several micrometers, and aggregate to form crystal clusters. In addition, small amounts of organic matters are found co-existing with Py-c. Results of n-alkanes analysis show that organic matters in Py-c consist mainly of microorganisms and terrestrial higher plants, indicating a possibility of forming Py-c by microorganisms which used terrestrial organic matters as electron donors. These systematic analyses indicate that Py-c in Tongling stratabound sulfide deposits was formed through biogeochemical-mediated sedimentation processes in a semi-enclosed sea basin. In Yanshanian period (Jurassic-Cretaceous), Py-c was transformed to macrocrystalline pyrite (Py-m) through recrystallization or to pyrrhotite and chalcopyrite through thermal metamorphism and mineral-fluid reaction. Py-c ores, which have high porosity, high chemical activity, and organic matter, could have played key roles in precipitating Cu and Au from Yanshanian magma-derived hydrothermal fluids and constrained the formation of stratabound sulfide orebodies in the Tongling mineralization cluster.