419 research outputs found

    Calculating the balance between atmospheric CO2 drawdown and organic carbon oxidation in subglacial hydrochemical systems

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    In order to constrain CO2 fluxes from biogeochemical processes in subglacial environments, we model the evolution of pH and alkalinity over a range of subglacial weathering conditions. We show that subglacial waters reach or exceed atmospheric pCO2 levels when atmospheric gases are able to partially access the subglacial environment. Subsequently, closed system oxidation of sulfides is capable of producing pCO2 levels well in excess of atmosphere levels without any input from the decay of organic matter. We compared this model to published pH and alkalinity measurements from 21 glaciers and ice sheets. Most subglacial waters are near atmospheric pCO2 values. The assumption of an initial period of open system weathering requires substantial organic carbon oxidation in only 4 of the 21 analyzed ice bodies. If the subglacial environment is assumed to be closed from any input of atmospheric gas, large organic carbon inputs are required in nearly all cases. These closed system assumptions imply that order of 10 g m−2 y−1 of organic carbon are removed from a typical subglacial environment—a rate too high to represent soil carbon built up over previous interglacial periods and far in excess of fluxes of surface deposited organic carbon. Partial open system input of atmospheric gases is therefore likely in most subglacial environments. The decay of organic carbon is still important to subglacial inorganic chemistry where substantial reserves of ancient organic carbon are found in bedrock. In glaciers and ice sheets on silicate bedrock, substantial long‐term drawdown of atmospheric CO2 occurs

    Quantitative bedrock geology of Brazil

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    Author Posting. © American Geophysical Union, 2007. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geochemistry Geophysics Geosystems 8 (2007): Q05014, doi:10.1029/2006GC001505.We quantitatively analyze the area-age distribution of sedimentary, igneous, metamorphic, and ultramafic bedrock on the basis of data from the digital geologic map of Brazil, published as a GIS map by the Brazilian Geological Survey. Bedrock units exclusively encompassing sedimentary rocks, igneous rocks, or metamorphic rocks cover 40.4%, 31.5%, and 17.7%, respectively, of the total bedrock area. These numbers have to be considered minimum estimates of the areal abundance of sedimentary, igneous, and metamorphic bedrock because polygons defined by mixed lithologies cover ~8.5–9.5% of the total bedrock area. These mixed units are sedimentary rocks with igneous and/or metamorphic contributions (1.4%), metamorphic rocks with sedimentary contributions (1.2%), metamorphic rocks with igneous contributions (1.5%), igneous rocks with sedimentary and/or metamorphic contributions (4.4%), and ultramafic units with sedimentary, igneous, and/or metamorphic contributions (~1–2%). The average ages of major lithologic units, weighted according to bedrock area, are as follows: sedimentary rocks (average stratigraphic age of 248 ± 5 [1σ] Myr; median stratigraphic age of 87.5 Myr), igneous rocks (1153 ± 13 [1σ] Myr), metamorphic rocks (1678 ± 30 [1σ] Myr), and ultramafic rocks (~1227 ± 25 [1σ] Myr). The average bedrock age of Brazil is 946 ± 7 [1σ] Myr. The range in lithologic composition and age structure of the various bedrock units reflects the complex tectonic makeup of Brazil that ranges from Neogene sedimentary cover in the Amazon Basin to Precambrian cratons (Guyana and Brazilian shields) and Transamazonian greenstone belts. The average spatial resolution of the data is 232 km2 polygon−1 and is sufficient to perform area-age analyses of individual river drainage basins larger than ~5,000 km2.B.P.E. acknowledges financial support from the U.S. National Science Foundation (NSF-EAR-0125873) and the Woods Hole Oceanographic Institution

    Cations extraction of sandy-clay soils from Cavado valley, Portugal, using sodium salts solutions

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    Cases of contamination by metals in the water wells of the Cavado Valley in north-west Portugal can be attributed to the heavy leaching of clay soils due to an excess of nitrogen resulting from the intensive use of fertilisers in agricultural areas. This work focuses on the natural weathering characteristics of soils, particularly the clay material, through the study of samples collected near the River Cavado. Samples taken from various sites, after physico-chemical characterisation, were subjected to clay dissolution tests, using sodium salts of different ionic forces, to detect the relationship between certain physico-chemical parameters of water, such as pH, nitrate, chloride and sulphate content, in the dissolution of clay and the subsequent extraction of such cations as Al, Fe and K. In acidic sandy clay soils, the mineralogical composition of which was characterised by a predominance of quartz, micas, kaolinite and K-feldspars, decreases of the clay material/water pH ratio increases dissolution of the micaceous and K-feldspars phases. The presence of nitrates in the aqueous solution apparently advanced the extraction of all three cations Al, Fe and K. The specific surface area of the clay material showed a significant correlation with the main kinetic parameters of cation extraction.TĂȘm ocorrido casos de contaminaçÔes de ĂĄguas de poços, por metais, no vale do Rio CĂĄvado, regiĂŁo noroeste de Portugal. A princĂ­pio, poderiam ser explicĂĄveis pela elevada lixiviação dos solos arenoargilosos da regiĂŁo, quando da prĂĄtica de adubaçÔes intensivas de nitrogĂȘnio em ĂĄreas agrĂ­colas. Assim, estudaram-se as caracterĂ­sticas do intemperismo natural dos solos, particularmente da fração argila, caracterĂ­stica da margem norte do rio CĂĄvado. Coletaram-se amostras de vĂĄrios locais, que foram submetidas, apĂłs caracterização fĂ­sico-quĂ­mica, a ensaios de dissolução a partir de soluçÔes de sais de sĂłdio com diferentes forças iĂŽnicas. O objetivo foi observar as relaçÔes de determinados parĂąmetros fĂ­sico-quĂ­micos da ĂĄgua, tais como: pH, nitratos, cloretos e sulfatos na dissolução das argilas e a conseqĂŒente extração de espĂ©cies quĂ­micas tais como Al, K e Fe. Para solos areno-argilosos, ĂĄcidos, cuja composição mineralĂłgica se caracteriza por um predomĂ­nio de quartzo, micas, caulinita e feldspato-K, o abaixamento do pH da suspensĂŁo solo/ĂĄgua promove a solubilização das fases micĂĄceas e feldspĂĄticas. A presença do nitrato nas soluçÔes aquosas promoveu aparentemente a extração de todos os trĂȘs cĂĄtions: Al, K e Fe. O efeito da ĂĄrea superfĂ­cial especĂ­fica das partĂ­culas dos solos condicionou fortemente vĂĄrios dos parĂąmetros cinĂ©ticos estudados relativos Ă  extração dos cĂĄtions.(undefined

    Unique Neoproterozoic carbon isotope excursions sustained by coupled evaporite dissolution and pyrite burial

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    The Neoproterozoic era witnessed a succession of biological innovations that culminated in diverse animal body plans and behaviours during the Ediacaran–Cambrian radiations. Intriguingly, this interval is also marked by perturbations to the global carbon cycle, as evidenced by extreme fluctuations in climate and carbon isotopes. The Neoproterozoic isotope record has defied parsimonious explanation because sustained 12C-enrichment (low ή13C) in seawater seems to imply that substantially more oxygen was consumed by organic carbon oxidation than could possibly have been available. We propose a solution to this problem, in which carbon and oxygen cycles can maintain dynamic equilibrium during negative ή13C excursions when surplus oxidant is generated through bacterial reduction of sulfate that originates from evaporite weathering. Coupling of evaporite dissolution with pyrite burial drives a positive feedback loop whereby net oxidation of marine organic carbon can sustain greenhouse forcing of chemical weathering, nutrient input and ocean margin euxinia. Our proposed framework is particularly applicable to the late Ediacaran ‘Shuram’ isotope excursion that directly preceded the emergence of energetic metazoan metabolisms during the Ediacaran–Cambrian transition. Here we show that non-steady-state sulfate dynamics contributed to climate change, episodic ocean oxygenation and opportunistic radiations of aerobic life during the Neoproterozoic era

    Soil vs. glass: an integrated approach towards the characterization of soil as a burial environment for the glassware of Cucagna Castle (Friuli, Italy)

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    This research is performed on a selection of archaeological glass finds with corresponding soil samples, excavated on the site of the High Medieval castle Cucagna in Friuli/Northern Italy. In the frame of understanding medieval glass technology and the chemical-physical conditions that influenced the state of preservation of the glass finds, this study uses a multi-analytical line-up of methods to characterize the composition of the glass and basic parameters of the soil including texture, mineralogical composition, pH, redox potential (Eh) and electric conductivity (EC). The results show that glass corrosion in soil not only depends on acidity, alkalinity or glass composition but also on the texture of the soil, measurable as grain-size distribution, and the mineralogical composition. The compositional groups of the glassware from Cucagna indicate the use of various raw material sources, pointing to Northern and Central Italian glass workshops with primary or secondary glass production.[GRAPHICS].FdA – Publicaties zonder aanstelling Universiteit Leide
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