1,081 research outputs found

    Porphyry copper enrichment linked to excess aluminium in plagioclase

    Get PDF
    PublishedPorphyry copper deposits provide around 75%, 50% and 20% of world copper, molybdenum and gold, respectively1. The deposits are mainly centred on calc-alkaline porphyry magmatic systems2, 3 in subduction zone settings1. Although calc-alkaline magmas are relatively common, large porphyry copper deposits are extremely rare and increasingly difficult to discover. Here, we compile existing geochemical data for magmatic plagioclase, a dominant mineral in calc-alkaline rocks, from fertile (porphyry-associated) and barren magmatic systems worldwide, barren examples having no associated porphyry deposit. We show that plagioclase from fertile systems is distinct in containing ‘excess’ aluminium. This signature is clearly demonstrated in a case study carried out on plagioclase from the fertile La Paloma and Los Sulfatos copper porphyry systems in Chile. Further, the presence of concentric zones of high excess aluminium suggests its incorporation as a result of magmatic processes. As excess aluminium has been linked to high melt water contents, the concentric zones may record injections of hydrous fluid or fluid-rich melts into the sub-porphyry magma chamber. We propose that excess aluminium may exclude copper from plagioclase, so enriching the remaining melts. Furthermore, this chemical signature can be used as an exploration indicator for copper porphyry deposits.The project would not have been possible without the financial and logistical support of Anglo American, including former and current staff: J. Coppard, V. Irarrazaval, M. Buchanan, E. Liebmann, R. Mattos Pino, E. Centino, J. Andronico, R. Mauricio, D. Fernando and J. Zamorano. J. Spratt (Natural History Museum, London) and S. Pendray (University of Exeter) are thanked for EPMA support and thin section preparation, respectively. K. Cashman (Bristol University), S. Hesselbo, J. Pickles and S. Broom-Fendley (University of Exeter), and reviewer J. Richards (University of Alberta), are gratefully acknowledged for comments on the manuscript

    A review of the potential for rare earth element resources from European red muds: examples from SeydiƟehir, Turkey and Parnassus-Giona, Greece

    Get PDF
    ArticleRare earth elements (REE) are viewed as ‘critical metals’ due to a complex array of production and political issues, most notably a near monopoly in supply from China. Red mud, the waste product of the Bayer process that produces alumina from bauxite, represents a potential secondary resource of REE. Karst-bauxite deposits represent the ideal source material for REE-enriched red mud as the conditions during formation of the bauxite allow for the retention of REE. The REE pass through the Bayer Process and are concentrated in the waste material. Millions of tonnes of red mud are currently stockpiled in onshore storage facilities across Europe, representing a potential REE resource. Red mud from two case study sites, one in Greece and the other in Turkey, has been found to contain an average of approximately 1 000 ppm total REE, with an enrichment of light over heavy REE. Although this is relatively low grade when compared with typical primary REE deposits (Mountain Pass and Mount Weld up to 80 000 ppm), it is of interest because of the large volumes available, the cost benefits of reprocessing waste, and the low proportion of contained radioactive elements. This work shows that around 12 000 tonnes of REE exist in red mud at the two case study areas alone, with much larger resources existing across Europe as a whole.The research leading to these results has received funding from the European 669 Community’s Seventh Framework Programme ([FP7/2007-2013]) under Grant 670 Agreement no. 309373

    Alkali-rich replacement zones in evolved NYF pegmatites: metasomatic fluids or immiscible melts?

    Get PDF
    IMA2018 Abstract submission Pegmatite mineralogy, geochemistry, classification and origins IMA2018-1337 Alkali-rich replacement zones in evolved NYF pegmatites: metasomatic fluids or immiscible melts? Axel Muller* 1, John Spratt2, Rainer Thomas3, Ben J. Williamson4, Reimar Seltmann2 1Natural History Museum, University of Oslo, Oslo, Norway, 2Department of Earth Sciences, Natural History Museum, London, United Kingdom, 3Chemistry and Physics of Earth Materials, German Research Centre for Geoscience GFZ, Potsdam, Germany, 4Camborne School of Mines, University of Exeter, Penryn, United Kingdom What is your preferred presentation method?: Oral or poster presentation : Replacement zones (RZ), which are a common feature of evolved granitic pegmatites, are irregular, commonly alkali-rich zones superimposing, cross-cutting and replacing the primary zonation in almost all consolidated pegmatite bodies. RZ are widely considered to result from late-stage metasomatism even though little is known about the melts and/or fluids involved in their formation. However, the observed textures and mineral paragenesis of RZ cannot be explained by metasomatism in a strict sense. In this study, the nature of the late stage silicate melt forming “cleavelandite” RZ is assessed from textural, mineralogical, chemical and melt inclusion studies of evolved, Proterozoic Niobium-Yttrium-Fluorine (NYF) rare metal pegmatites from Evje–Iveland, southern Norway. These were studied as they are mineralogically simple, compared with RZ in evolved Lithium-Caesium-Tantalum (LCT) pegmatites. Silicate melt inclusions in RZ-forming topaz and “cleavelandite” document high H2O contents of up to18 wt.% of the F-rich silicate melt from which the RZ crystallized. In addition, from mineral compositions (“cleavelandite”, “amazonite”, white mica, garnet, columbite group minerals, topaz, fluorite, and beryl), they must have also been strongly alkaline (Na-dominated) with enrichments in F (at least 4 wt.%), Cs, Rb, Ta, Nb, Mn, Ge, Bi, As, and in some cases also Li compared with host pegmatites. These elements are concentrated in a few RZ-forming minerals resulting in very distinctive mineral-trace element signatures. “Amazonite” is strongly enriched in Cs and Rb and often white mica and beryl in Li and Cs. To acquire these mineral compositions, the overall Li-Cs-Ta-poor Evje-Iveland original pegmatite melt must have undergone extreme internal chemical differentiation resulting in melt/melt immiscibility aiding rheology contrasts and resulting in RZ formation. The resulting RZ-forming H2O-F-rich silicate melt would have shown large differences in viscosity and density, and therefore physical flow/transport properties, to the host pegmatite melt resulting in discordant contacts. The mineralogy and melt inclusion data from the Evje-Iveland pegmatites document a gradient of crystallization temperatures within the investigated pegmatite bodies with highest temperatures at the pegmatite margin (during initial emplacement, ~680°C) and lowest temperatures within the RZ (<500°C). Considering the temperature and pressure conditions of the host rocks gneisses and amphibolites (~650°C, up to 5 kbar) at the time of pegmatite emplacement and the crystallization conditions of the RZ, the Evje- Iveland pegmatites and RZ likely formed over a period of 2.2 million years, assuming an exhumation rate of 1.5 mm per million years and a geothermal gradient of 45°C km-1. Such a long crystallization time contradicts the classical view that pegmatites represent strongly undercooled melts which crystallize relatively fast.The attached document is the authors’ submitted version of the oral presentation. You are advised to consult the publisher’s version if you wish to cite from it

    Apatite texture and composition in the Tonglushan porphyry-related skarn system, eastern China: implications for mineral exploration

    Get PDF
    This is the final version. Available on open access from Elsevier via the DOI in this recordData availability: Data will be made available on request.The composition of ‘indicator’ minerals is thought to provide a guide to the potential of magmatic arc systems to form porphyry Cu deposits, but whether this is also the case for endoskarn- and exoskarn-dominated systems remains unclear, despite their importance as a source of Cu, Fe and Au. In a first step to address this, we compare the texture, cathodoluminescence (CL) colour and composition of apatite between relatively fresh quartz monzodiorite (QMD) and porphyry-type-, endoskarn- and Fe-(Cu)-mineralised exoskarn components of the Tonglushan porphyry-skarn system of the Daye ore district, China. In the relatively fresh QMD, apatite luminesces yellow-green due to elevated Mn contents. However, where affected by potassic-sodic alteration, it shows green–blue CL thought to reflect partial removal of Mn and an associated increase in REE. Apatite in the endoskarn is more pervasively replaced and veined, and shows mid-blue luminescence due to relatively low Mn, Mg and Cl. The exoskarns contain apatite with variable grain shapes and navy blue-violet or bright to dark blue CL colours, caused by low Mn and elevated Ce, and with only small patches of pale yellow-green CL. Apatite is near absent in the limestone wall rocks and xenoliths and, therefore, where present in the exoskarns is interpreted to have precipitated from the same fluids as the Fe-(Cu) mineralization. Apatite CL colour and chemistry is indicative of the different styles of alteration and mineralisation in the Tonglushan system and provides insights into the composition of skarn-forming fluids. Our results offer a potentially effective method for utilising apatite as a porphyry and skarn deposit indicator mineral in a range of exploration materials including regolith and stream sediments.China Scholarship CouncilUniversity of ExeterNatural Environment Research Council (NERC

    First Detection of Mycobacterium ulcerans DNA in Environmental Samples from South America

    Get PDF
    The occurrences of many environmentally-persistent and zoonotic infections are driven by ecosystem changes, which in turn are underpinned by land-use modifications that alter the governance of pathogen, biodiversity and human interactions. Our current understanding of these ecological changes on disease emergence however remains limited. Buruli ulcer is an emerging human skin disease caused by the mycobacterium, Mycobacterium ulcerans, for which the exact route of infection remains unclear. It can have a devastating impact on its human host, causing extensive necrosis of the skin and underlying tissue, often leading to permanent disability. The mycobacterium is associated with tropical aquatic environments and incidences of the disease are significantly higher on floodplains and where there is an increase of human aquatic activities. Although the disease has been previously diagnosed in South America, until now the presence of M. ulcerans DNA in the wild has only been identified in Australia where there have been significant outbreaks and in western and central regions of Africa where the disease is persistent. Here for the first time, we have identified the presence of the aetiological agent's DNA in environmental samples from South America. The DNA was positively identified using Real-time Polymerase Chain Reaction (PCR) on 163 environmental samples, taken from 23 freshwater bodies in French Guiana (Southern America), using primers for both IS2404 and for the ketoreductase-B domain of the M. ulcerans mycolactone polyketide synthase genes (KR). Five samples out of 163 were positive for both primers from three different water bodies. A further nine sites had low levels of IS2404 close to a standard CT of 35 and could potentially harbour M. ulcerans. The majority of our positive samples (8/14) came from filtered water. These results also reveal the Sinnamary River as a potential source of infection to humans. © 2014 Morris et al

    The transition from granite to banded aplite-pegmatite sheet complexes: An example from Megiliggar rocks, Tregonning topaz granite, Cornwall

    Get PDF
    This is the author accepted manuscript. The final version is available from Elsevier via the DOI in this record.The genetic relationship between a granite pluton and adjacent complex of rare-metal pegmatite-aplite-banded sheets (Megiliggar Sheet Complex - MSC) has been studied at the border of the Tregonning topaz granite at Megiliggar Rocks, Cornwall, SW England. Similarities in whole-rock chemical and mineralogical compositions, together with a gradual change in textures away from the granite margin, provide strong evidence for a genetic link between the Tregonning Granite and MSC. The sheets are likely to represent apophyses of residual melt which escaped from the largely crystallised roof of the granite pluton. The escaping melt was peraluminous, had a composition near the F, B, Li slightly enriched granite minimum, and, in comparison with other Cornish granites, was enriched in F, Li, Rb, Cs, Sn, W, Nb, Ta, and U, and depleted in Fe, Mg, Ca, Sr, Th, Zr, and REE. With increasing distance from the Tregonning Granite, the silicate melt crystallised as homogeneous leucogranite sheets and banded complex sheets (i.e. combinations of bands with granitic, aplitic and pegmatitic textures), then layered aplite-pegmatites; this sequence becoming progressively more depleted in the fluxing and volatile elements F, Li, Rb, and Cs, but showing no change in Zr/Hf ratios. The fixed Zr/Hf ratio is interpreted as indicating a direct genetic link (parental melt) between all rock types, however the melt progressively lost fluxing and volatile elements with distance from the granite pluton, probably due to wall-rock reaction or fluid exsolution and migration via fractures. Differentiation of the primary melt into Na-Li-F-rich and separate K-B-rich domains was the dominant chemical process responsible for the textural and mineral diversity of the MSC. On a large (cliff-section) scale, the proximal Na-Li-F-rich leucogranite passes through complex sheets into K-B-rich aplite-pegmatites, whilst at a smaller (< 1 m) scale, the K-B-rich bands are interspersed (largely overlain) by Na-Li-F-rich segregations. The grain size differences between the aplite and pegmatite could be related to pressure fluctuations and/or undercooling.Laser-ablation ICP-MS analyses of micas and tourmaline in Masaryk University Brno were supported by the Czech Science Foundation project No. GA14-13600S. All other analytical work for this contribution was supported by the RVO 67985831 in the Institute of Geology of the Czech Academy of Sciences, Praha. We are grateful to P. Davidson and an anonymous referee for their reviews

    Selection of operational parameters for a smart spraying system to control airborne PM10 and PM2.5 dusts in underground coal mines

    Get PDF
    This is the author accepted manuscript. The final version is available from Elsevier via the DOI in this recordAirborne dust in underground hard coal mines is an ongoing explosion and respiratory health hazard. The latest design solution for controlling dusts, the smart spraying system, is described. From the results of stand tests, the main factors determining the efficiency of the new device are: 1) the integrated real-time acquisition of dust particle size and concentration data, determined using a new optical dust meter; 2) the fractional distribution of water droplets; and 3) the selection of droplet size to capture PM10 and PM2.5. The latter two factors are automatically controlled, based on dust measurements, by varying the pressure of water and compressed air supplied to the sprayer nozzles. The effects of varying these parameters and the results of stand tests are presented. The spraying device was tested for the effectiveness of PM2.5 dust and PM10 dust reduction in underground conditions in the KWK PniĂłwek mine. The tests were based on the following Polish Standards: PN-91/Z-04030/05 and PN91/Z-04030/06, which define the methodology for measurements of inhalable and respirable dust at workplaces using the filtration-weighing method to determine the concentration of inhalable and respirable dust with the spraying system on and off. The results showed that the assumed objective, i.e. development of a dust control device that would reduce PM2.5 dust (by min. 25 %) and PM10 dust (by min. 20 %) more effectively than the currently used solutions, was achieved in the project. At the same time, the device, due to application of dust sensor, continuously adjusts the parameters of spraying streams to the dust concentration level, optimizing the consumption of water and compressed air. Similar results in reduction of PM10 and PM2.5 dust, with an average effectiveness of over 60 % is the undoubted advantage of the device.European Commission Research Fund for Coal and Stee
    • 

    corecore