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Hexavalent chromium (Cr6+) is a toxic carcinogenic pollutant that might be released by the mining and processing of ultramafic rocks and nickel laterites and which requires permanent removal from the contaminated biosphere. Ultramafic material can also serve as a feedstock for the sequestration of CO2 resulting from the growth of new minerals, raising the intriguing proposition of integrated sequestration of both pollutants, CO2 and chromium, into magnesium carbonates. Such a synergistic process downstream of ore recovery and mineral processing could be an elegant proposition for more sustainable utilisation and management of the Earth's resources. We have therefore carried out an experimental and microanalytical study to investigate potentially suitable carbonate minerals. Uptake of chromium in carbonate phases was determined, followed by identification of the crystalline phases and characterisation of the local structural environment around the incorporated chromium centres. The results suggest that neither nesquehonite nor hydromagnesite have the structural capacity to incorporate Cr6+ or Cr3+ significantly at room temperature. We therefore propose that further research into this technology should focus on laboratory assessments of other phases, such as layered double hyroxides, that have a natural structural capacity to uptake both chromium and CO2.

Primary mining of technology metal ores is needed to enable effective decarbonisation. The use of nickel in rechargeable batteries is expected to increase global demand for nickel rapidly over the coming years. Over 60% of annual global nickel production originates from nickel laterites, with Indonesia and the Philippines leading the market. Mining of nickel laterite ore can adversely affect the environment through the release of CO2 and potentially hazardous elements (PHE), such as hexavalent chromium, or asbestiform minerals. Through our better understanding of the social and environmental impacts of mining operations and the availability of technologies that can potentially mitigate adverse impact, it is paramount to aim for more responsible mining and metal recovery operations. This study focuses on the Sta Cruz nickel laterite deposit in the Philippines. Through a multi-scale and multi-technique analytical programme and drawing on existing knowledge1,2, we appraise the deposit holistically, focusing on (i) the geochemistry and mineralogy of major commodities and trace metals, such as the platinum group elements; (ii) carbonate forming metals, e.g. magnesium and (iii) the presence and ecotoxicity of PHE and minerals. We use this understanding to assess the potential for a circular economy in mining, via complete utilisation of the ore to maximise the metal output and minimise the waste produced. This includes the removal of CO2 through the formation of carbonate minerals (mineral carbonation). We also investigate the potential of carbonates to immobilise chromium crystallographically alongside the CO2. This aspect of mineral carbonation is currently poorly understood. We have carried out laboratory synthesis of chromium-doped carbonates at ambient P-T conditions, which indicates that the most common magnesium carbonates do not readily accommodate chromium. However, other carbonate-bearing minerals, including those belonging to layered double hydroxides, present

Significant theoretical storage capacity is available in saline aquifer formations, however there is a need to transition these from undiscovered to discovered storage resources if we are to meet climate targets. Unlocking this considerable storage resource requires considerable effort in terms of time, money and resources. The Storage Readiness Level concept provides a useful indication of the technical activities required to mature prospective storage sites towards development. The process is underway for the UK Bunter Sandstone saline aquifer, with several carbon storage licences issued, which include substantive obligations to acquire new data to de-risk the storage resource. Comprehensive understanding at both site and regional scales will be required to manage the storage resource effectively. Regional studies such as those underway at the British Geological Survey will support commercial efforts to unlock the storage capacity of the Bunter Sandstone.

Correct interpretation of soft-bodied fossils relies on a thorough understanding of their taphonomy. While the focus has often been on the primary roles of decay and early diagenesis, the impacts of deeper burial and metamorphism on fossil preservation are less well understood. We document a sequence of late-stage mineral replacements in panarthropod fossils from the Sirius Passet Lagerstätte (North Greenland), an important early Cambrian Burgess Shale–type (BST) biota. Muscle and gut diverticula were initially stabilized by early diagenetic apatite, prior to being pervasively replaced by quartz and then subordinate chlorite, muscovite, and chloritoid during very low- to low-grade metamorphism. Each new mineral replicates the soft tissues with different precision and occurs in particular anatomical regions, imposing strong biases on the biological information retained. Muscovite and chloritoid largely obliterate the tissues’ original detail, suggesting that aluminum-rich protoliths may have least potential for conserving mineralized soft tissues in metamorphism. Overall, the fossils exhibit a marked shift toward mineralogical equilibration with the matrix, obscuring primary taphonomic modes. Sequential replacement of the phosphatized soft tissues released phosphorus to form new accessory monazite (and apatite and xenotime), whose presence in other BST biotas might signal the prior, more widespread, occurrence of this primary mode of preservation. Our results provide critical context for interpreting the Sirius Passet biota and for identifying late-stage overprints in other biotas.

Fractures within hydrothermal systems represent major pathways for fluid flow, and it is therefore vital that we understand processes occurring along them as these may have an impact on productivity of hot fluids during geothermal exploitation. This is especially important where hydrothermal activity crosses contrasting rock types, as fluid movement can result in a range of fluid�rock reactions, mineral dissolution and precipitation, and possible changes in fracture permeability. Here we report evidence of fluid-rock reactions within basement carbonates and overlying volcanic rocks within hydrothermally altered rocks of the eastern trans-Mexico volcanic belt, as part of the Europe-Mexico collaborative ‘GEMex’ project (EU-H2020, GA No. 727550). Identified reactions within basement carbonates include initial high temperature Si-metasomatism linked to igneous intrusions to form minerals such as olivine, wollastonite, garnet and diopside, followed by subsequent lower temperature hydration (back reaction) at lower temperatures, where olivine and diopside hydrate to form serpentine and talc. Reactions of overlying andesitic units include Ca-metasomatism and bleaching through interaction of rising acidic, carbonate-equilibrated fluids. Secondary minerals produced during these reactions appear to seal fractures, implying tectonic reactivation of fractures to maintain long-term fluid flow through fracture zones.

A light REE (LREE)-bearing mineral called chevkinite (Ce, La, Ca, Th)4(Fe2+, Mg)2(Ti, Fe3+)3Si4O22, originating from a heavy metal placer deposit Aksu Diamas in Turkey, previously assessed for potential REE extraction as a by-product of magnetite production, was studied using scanning electron microscopy with energy and wavelength-dispersive spectrometers (SEM EDS-WDS). This mineral exhibits analytical challenges associated with severe X-ray energy overlaps between the REE, titanium, and barium. Here, we present an iterative process, showing that SEM EDS-WDS is a viable technique for obtaining good quality quantitative data. SEM EDS-WDS is an in situ, non-destructive, and relatively non-expensive technique, but operator’s experience is essential to obtain good quality data. In cases where the peak fitting remains challenging, in particular, and where the constituents have large differences in abundance, an assessment of the X-ray spectrum to qualitatively assign all peaks is essential prior to quantitative analysis

Silica cementation exerts a key control on the compaction and geotechnical properties of mudstones, and by extension, the style of hydrocarbon and/or mineral systems present in a given sedimentary basin. Integrated microscopic and bulk geochemical observations demonstrate that siliceous mudstones in the Bowland Shale Formation, a target for UK shale gas extraction, exhibit abundant dispersed, discrete, μm-scale quartz cements, and exhibit silica enrichment (‘excess’) above a local detrital Si/Al threshold of 2.5. Dissolution of siliceous radiolarian tests during early diagenesis is identified as the main source of silica (opal A) required for quartz precipitation, either via opal CT or directly to quartz, and potentially generated as a product of anoxic marine ‘weathering’ (dissolution) of reactive silicates during early diagenesis. Excess silica correlates with free hydrocarbons (S1) normalised to total organic carbon (oil saturation index; OSI); we propose early diagenetic quartz precipitation suppressed pore collapse (‘buttress effect’), retaining the pore space capacity to host oil. Quartz precipitation was likely catalysed, for example via low porewater pH, elevated Al and/or Fe oxide content, and/or abundant labile organic matter. Juxtaposition of siliceous mudstones and mudstones lacking quartz cement indicates silica was immobile beyond the bed scale. Thus metre-scale siliceous packages likely represent more prospective units within the Bowland Shale (in terms of unconventional hydrocarbons), on the basis of early diagenetic biogenic-derived quartz cementation leading to improved hydrocarbon storage capacity coupled to enhanced brittleness. These findings are relevant for shale oil and shale gas systems, specifically where oil retained in pores subsequently cracks to generate gas. These findings also suggest the Bowland Shale is a sub-class of black shale, defined by the potential to host a relatively large volume of early diagenetic fluids, derived from ano

Improving our ability to predict the interactions between CO2 and reservoir rocks at geological time scales is of key importance if carbon capture and storage (CCS) is to have a role in climate-change mitigation, particularly in the light of likely regulatory requirements. Understanding and identifying the relevant geological processes over long time scales can be obtained only at natural-analogue sites. At one such site, in the Salt Wash Graben area of Utah, USA, widespread bleaching affects the Middle Jurassic red-bed “wet dune” Entrada Sandstone. Previous work has proposed a genetic link between the bleaching and spatially concomitant recent and modern CO2-rich fluids. The results presented here challenge some of the previous models and come from a detailed petrographic examination of mineralized fractures in the Entrada Sandstone that are centered in vertical extensions to the bleaching. These fractures typically contain complex mineralization assemblages. Pyrite was a paragenetically early phase, identifiable from common pseudomorphs of mixed iron oxides and oxyhydroxides that rarely contain relict pyrite. The pyrite contains up to 3 wt% arsenic. The volume of fracture-adjacent bleached sandstone is sufficient to have been the source of iron for the pyrite originally present in the fracture. The pyrite pseudomorphs occur at the center of fracture- and pore-filling cements that comprise intergrowths of hematite–goethite–jarosite–gypsum, an assemblage that suggests that their formation resulted from the oxidative alteration of pyrite, a genetic link supported by the arsenic present in the iron-bearing minerals. The presence of jarosite and proximal removal of earlier, sandstone-hosted carbonates are consistent with, and indicative of, the low-pH conditions associated with pyrite oxidation reactions. Calcite- and gypsum-cemented fractures crosscut, and contain fragments of, the pyrite-pseudomorphic and -oxidation assemblages, proving that they postdate pyrite form

The rare mineral kalistrontite, K 2 Sr(SO 4 ) 2 , has been discovered in exceptional quantities in exploration boreholes targeting Permian polyhalite [K 2 Ca 2 Mg(SO 4 ) 4 ·2(H 2 O)]-bearing evaporite deposits in North Yorkshire, U.K. The ka - listrontite is associated with anhydrite, polyhalite, halite, magnesite, and traces of celestine in the Fordon (Evaporite) Formation, English Zechstein 2 cycle, at depths of ~1.5 to 1.7 km below surface. It was first encountered here during quantitative X-ray diffraction assays of composited drill-core samples over an identified ~50 m interval in York Potash Ltd.’s boreholes SM6, SM9, and deflections SM9A and 9B. X-ray diffraction including structural refinement, thermal analysis, Raman spectroscopy, petrographic examina - tion, quantitative microanalysis, and Sr isotopic analysis have been employed to fully characterize the kalistrontite and determine its genesis to understand its distribution and significance for the polyhalite deposits. Petrographic examination reveals that the kalistrontite is present in two general forms. First as irregularly shaped, poikilotopic millimeter-scale patches of subhedral, equant to elongate millimeter-scale crystals that enclose fine, rounded, irregular anhedral and rarely euhedral crystals of anhydrite, halite, and magnesite. Second as a vein-fill formed of an interlocking mosaic of elongate sub-millimeter scale, euhedral crystals that are compositionally zoned and again enclose fine rounded anhydrite and halite crystals at vein margins. Kalistrontite displays largely replacive contact relationships with both the earlier and generally simultaneously formed anhydrite and halite but before at least some of the polyhalite. Vein-fill kalistrontite was deposited by mineralizing fluids proceeding along fractures, patchily replacing the pre-existing low-porosity anhydrite and halite. EDX microanalysis of the North Yorkshire kalistrontite indicates a purer composition than previously reported but so

SUMMARY: Subsurface 3D geological models of aquifer and seal rock systems from two contrasting analogue sites have been created as the first step in an investigation into methodologies for geological storage of carbon dioxide in saline aquifers. Development of the models illustrates the utility of an integrated approach using digital techniques and expert geological knowledge to further geological understanding. The models visualize a faulted, gently dipping Permo-Triassic succession in Lincolnshire and a complex faulted and folded Devono-Carboniferous succession in eastern Scotland. The Permo-Triassic is present in the Lincolnshire model to depths of 2 km OD, and includes the aquifers of the Sherwood Sandstone and Rotliegendes groups. Model-derived thickness maps test and refine Permian palaeogeography, such as the location of a carbonate reef and its associated seaward slope, and the identification of aeolian dunes. Analysis of borehole core samples established average 2D porosity values for the Rotliegendes (16%) and Sherwood Sandstone (20%) groups, and the Zechstein (5%) and Mercia Mudstone (<10%) groups, which are favourable for aquifer and seal units respectively. Core sample analysis has revealed a complex but well understood diagenetic history. Re-interpretation of newly reprocessed seismic data in eastern Scotland has significantly reduced interpretative uncertainty of aquifer and seal units at depths of up to 6 km OD in a complex faulted and folded Devonian-Carboniferous succession. Synthesis of diverse data in the 3D geological model defines a set of growth folds and faults indicative of active Viséan to Westphalian dextral-strike slip, with no major changes in structural style throughout the Carboniferous, in contrast to some published tectonic models. Average 2D porosity values are 14-17% in aquifer units and <2% in the seal unit, with a ferroan dolomite cement occluding porosity at depth.

Brachiopod carbonate from Early Permian brachiopod shells from low palaeolatitude north Iran and higher palaeolatitude Pakistan Karakorum were screened for diagenesis and analysed for oxygen isotope ratios to derive seawater palaeotemperatures. Screening techniques employed included SEM ultrastuctural analysis, cathodoluminescence (CL), image analysis of CL images, trace-element (Sr, Mn, Fe) determinations, and carbon and oxygen stable-isotope determinations. The Karakorum shells were found to be diagenetically altered, but those from north Iran were judged to be pristine. Using data from pristine material, two distinct time slices were analysed: the early and middle Asselian. The maximum calculated temperatures in the middle Asselian are about 2 oC lower than those for the early Asselian. The average temperature for both time slices is similar to modern tropical sea-surface temperatures, indicating that low-latitude Early Permian ocean waters in Iran did not undergo significant cooling during the final Glacial III episode of Gondwanan glaciation. This confirms other evidence based on biotic provinces, which suggests that during the Permo-Carboniferous glaciation, the low-latitude warm belt became narrower and confined to the western Tethys and Cathaysian provinces, and was not subject to a reduction in temperature, but rather a reduction in size.