756 research outputs found

    Long-term evolution of highly alkaline steel slag drainage waters

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    © 2015, Springer International Publishing Switzerland. The disposal of slag generated by the steel industry can have negative consequences upon the surrounding aquatic environment by the generation of high pH waters, leaching of potentially problematic trace metals, and rapid rates of calcite precipitation which smother benthic habitats. A 36-year dataset was collated from the long-term ambient monitoring of physicochemical parameters and elemental concentrations of samples from two steel slag leachate-affected watercourses in northern England. Waters were typified by elevated pH ( > 10), high alkalinity, and were rich in dissolved metals (e.g. calcium (Ca), aluminium (Al), and zinc (Zn)). Long-term trend analysis was performed upon pH, alkalinity, and Ca concentration which, in addition to Ca flux calculations, were used to highlight the longevity of pollution arising as a result of the dumping and subsequent leaching of steel slags. Declines in calcium and alkalinity have been modest over the monitoring period and not accompanied by significant declines in water pH. If the monotonic trends of decline in alkalinity and calcium continue in the largest of the receiving streams, it will be in the region of 50–80 years before calcite precipitation would be expected to be close to baseline levels, where ecological impacts would be negligible

    PFAS River Export Analysis Highlights the Urgent Need for Catchment-Scale Mass Loading Data

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    Source apportionment of per-and polyfluoroalkyl substances (PFAS) requires an understanding of the mass loading of these compounds in river basins. However, there is a lack of temporally variable and catchment-scale mass loading data, meaning identification and prioritization of sources of PFAS to rivers for management interventions can be difficult. Here, we analyze PFAS concentrations and loads in the River Mersey to provide the first temporally robust estimates of PFAS export for a European river system and the first estimates of the contribution of wastewater treatment works (WwTWs) to total river PFAS export. We estimate an annual PFAS export of 68.1 kg for the River Mersey and report that the yield of perfluorooctanesulfonic acid (PFOS) and perfluorooctanoic acid (PFOA) in the catchment is among the highest recorded globally. Analysis of river and WwTW loads indicates approximately one-third of PFOA emitted from WwTWs is potentially stored in the catchment and approximately half of PFOS transported by the River Mersey may not originate from WwTWs. As governments move toward regulation of PFAS in WwTW effluents, our findings highlight the complexity of PFAS source apportionment and the need for catchment-scale mass loading data. This study indicates that strategies for reducing PFAS loading that focus solely on WwTW effluents may not achieve river water quality targets

    Narrow-band anisotropic electronic structure of ReS2

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    We have used angle-resolved photoemission spectroscopy to investigate the band structure of ReS 2, a transition-metal dichalcogenide semiconductor with a distorted 1T crystal structure. We find a large number of narrow valence bands, which we attribute to the combined influence of structural distortion and spin-orbit coupling. We further show how this leads to a strong in-plane anisotropy of the electronic structure, with quasi-one-dimensional bands reflecting predominant hopping along zigzag Re chains. We find that this does not persist up to the top of the valence band, where a more three-dimensional character is recovered with the fundamental band gap located away from the Brillouin zone center along kz. These experiments are in good agreement with our density-functional theory calculations, shedding light on the bulk electronic structure of ReS2, and how it can be expected to evolve when thinned to a single layer

    Quantifying CO2 Removal at Enhanced Weathering Sites: a Multiproxy Approach

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    Enhanced weathering is a carbon dioxide (CO 2) mitigation strategy that promises large scale atmospheric CO 2 removal. The main challenge associated with enhanced weathering is monitoring, reporting, and verifying (MRV) the amount of carbon removed as a result of enhanced weathering reactions. Here, we study a CO 2 mineralization site in Consett, Co. Durham, UK, where steel slags have been weathered in a landscaped deposit for over 40 years. We provide new radiocarbon, δ 13 C, 87 Sr/ 86 Sr, and major element data in waters, calcite precipitates, and soils to quantify the rate of carbon removal. We demonstrate that measuring the radiocarbon activity of CaCO 3 deposited in waters draining the slag deposit provides a robust constraint on the carbon source being sequestered (80% from the atmosphere, 2σ = 8%) and use downstream alkalinity measurements to determine the proportion of carbon exported to the ocean. The main phases dissolving in the slag are hydroxide minerals (e.g., portlandite) with minor contributions (<3%) from silicate minerals. We propose a novel method for quantifying carbon removal rates at enhanced weathering sites, which is a function of the radiocarbon-apportioned sources of carbon being sequestered, and the proportion of carbon being exported from the catchment to the oceans

    Narrow-band anisotropic electronic structure of ReS2

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    We have used angle resolved photoemission spectroscopy to investigate the band structure of ReS2, a transition-metal dichalcogenide semiconductor with a distorted 1T crystal structure. We find a large number of narrow valence bands, which we attribute to the combined influence of the structural distortion and spin-orbit coupling. We further image how this leads to a strong in-plane anisotropy of the electronic structure, with quasi-one-dimensional bands reflecting predominant hopping along zig-zag Re chains. We find that this does not persist up to the top of the valence band, where a more three-dimensional character is recovered with the fundamental band gap located away from the Brillouin zone centre along kz. These experiments are in good agreement with our density-functional theory calculations, shedding new light on the bulk electronic structure of ReS2, and how it can be expected to evolve when thinned to a single layer.PostprintPeer reviewe

    Evolution of an accretionary complex (LeMay Group) and terrane translation in the Antarctic Peninsula

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    The LeMay Group accretionary complex of Alexander Island (Antarctic Peninsula) comprises a 4 km thick succession of variably deformed turbidites associated with thrust slices of ocean floor basalts. The depositional age and provenance of the succession is uncertain with estimates ranging from Carboniferous to Cretaceous. The accretion history is also poorly established and whether the LeMay Group developed allochthonously and accreted during an episode of Cretaceous terrane translation. We have examined the geochronology and geochemistry of twenty-two samples from across the entire accretionary complex to determine its depositional, provenance and accretion history. The accretionary complex has been subdivided into four separate groups based on detrital zircon U-Pb age and Lu-Hf provenance analysis. Groups 1 and 2 are interpreted to be a continuation of the extensive Permian accretionary complexes of West Gondwana and have a depositional age of c. 255 Ma, with volcaniclastic input from the extensive silicic volcanism of the Choiyoi Province. Accretion of the LeMay Group to the continental margin developed during the mid-Triassic, potentially related to the Peninsula Orogeny and an episode of flat-slab subduction of the proto-Pacific plate. Group 3 is only identified from an island to the west of Alexander Island and has a mid-Cretaceous depositional age and provenance akin to offshore sequences from Thurston Island. A para-autochthonous origin is suggested, with mid-Cretaceous accretion associated with the melange belts of central Alexander Island. Group 4 is also a distinct unit with an Early Jurassic depositional age and a source more closely related to the Antarctic Peninsula

    Palaeozoic – Early Mesozoic geological history of the Antarctic Peninsula and correlations with Patagonia: Kinematic reconstructions of the proto-Pacific margin of Gondwana

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    The Antarctic Peninsula preserves geological evidence of a long-lived continental margin with intrusive, volcaniclastic and accretionary complexes indicating a convergent margin setting from at least the Cambrian to the Cenozoic. We examine the poorly understood units and successions from the Palaeozoic to the Early Mesozoic and develop detailed kinematic reconstructions for this section of the margin. We use existing geochronology, along with newly presented Usingle bondPb detrital zircon geochronology, combined with detailed field evidence to develop correlations between geological units and tectonic events across Patagonia and the proto-Antarctic Peninsula. The continental margin of Gondwana/Pangea was a convergent margin setting punctuated by crustal block translation, deformation, magmatic pulses (flare-ups) and development of thick accretionary complexes. These events are strongly linked to subducting slab dynamics and a para-autochthonous model is proposed for the long-lived margin. Major magmatic pulses are evident during the Ordovician (Famatinian) and Permian, and the magmatic record is reflected in the detrital zircon age profiles of metasedimentary successions of the northern Antarctic Peninsula and Tierra del Fuego. Major tectonic events during the Carboniferous – Permian (Gondwanide Orogeny) and Triassic (Chonide Event – Peninsula Orogeny) are recognised across the Antarctic Peninsula – Patagonia and are correlated to potential terrane suturing and flat slab dynamics. Our kinematic reconstructions developed in GPlates, combined with geological field relationships have allowed us to model the locus of magmatism relative to the active margin and also the likely source for thick sedimentary successions

    Reuse of structural domain–domain interactions in protein networks

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    <p>Abstract</p> <p>Background</p> <p>Protein interactions are thought to be largely mediated by interactions between structural domains. Databases such as <it>i</it>Pfam relate interactions in protein structures to known domain families. Here, we investigate how the domain interactions from the <it>i</it>Pfam database are distributed in protein interactions taken from the HPRD, MPact, BioGRID, DIP and IntAct databases.</p> <p>Results</p> <p>We find that known structural domain interactions can only explain a subset of 4–19% of the available protein interactions, nevertheless this fraction is still significantly bigger than expected by chance. There is a correlation between the frequency of a domain interaction and the connectivity of the proteins it occurs in. Furthermore, a large proportion of protein interactions can be attributed to a small number of domain interactions. We conclude that many, but not all, domain interactions constitute reusable modules of molecular recognition. A substantial proportion of domain interactions are conserved between <it>E. coli</it>, <it>S. cerevisiae </it>and <it>H. sapiens</it>. These domains are related to essential cellular functions, suggesting that many domain interactions were already present in the last universal common ancestor.</p> <p>Conclusion</p> <p>Our results support the concept of domain interactions as reusable, conserved building blocks of protein interactions, but also highlight the limitations currently imposed by the small number of available protein structures.</p
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