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111.
Abstract Fluids and sediments from Deep Sea Drilling Project/Ocean Drilling Program Legs (56, 57, 87 and 186) along a transect extending from the subducting plate, across the midslope and upper slope of the Japan Trench forearc were analyzed for B and B isotopes in order to assess their composition and fluid–sediment interaction. At the reference Site 436 on the subducting plate, changes in B contents and B isotopes are controlled by the lithology and diagenesis only. The midslope Sites 440 and 584 showed stronger variations in the B geochemistry, which can be related to diagenesis and tectonic dewatering along faults. The strongest changes in the B geochemistry were observed on the upper slope Sites 1150 and 1151, where profound down‐hole freshening (chlorinities as low as ~310 mmol) coincides with a B enrichment (up to 9.3 × seawater concentration). The B isotope pore fluid profile of Site 1150 displayed a bimodal variation with depth, first increasing to values more positive than seawater, then shifting to lower signatures typical for deep‐seated fluids, whereas Site 1151 showed a constant B decrease with depth. Sites 1150 and 1151 sediments showed B increases with depth to values as high as ~164 p.p.m. and isotopic compositions ranging from ~+4 to ?9‰. A linear decrease in Bsolid/Bfluid ratio, suggests that B geochemistry of the upper slope sites is controlled by fluid–rock interaction and deep‐seated fluid flow, whereas constant Bsolid/Bfluid ratios were observed at the reference site on the incoming plate. This fluid overprint is probably caused by normal faults in the sediment cover which might be interconnected to deep thrusts in the underlying Cretaceous accreted wedge. This suggests that the erosive Japan Trench margin is characterized by back‐flux of deep‐seated, B‐enriched fluids into the ocean, which is facilitated by extensional normal faulting as a result of tectonic erosion and subsidence.  相似文献   
112.
This investigation used two approaches to examine the flux of bank-derived carbonate particles and determine the potential influence of benthic carbonate particle dissolution on the carbon chemistry of the waters around the Hawaiian Archipelago. First, the particle flux near several representative carbonate banks in the Hawaiian Archipelago was measured and compared with the flux at a distal site (ALOHA) approximately 100 km north of Oahu, Hawaii. The results of four sediment trap deployments on three carbonate banks in the Hawaiian Archipelago demonstrate that the flux of bank-derived carbonate particles are consistently one to two orders of magnitude higher than the fluxes at the distal station. Furthermore, the mineralogy of the carbonate flux near the banks, which includes very soluble bank-derived aragonite and magnesian calcite particles, is distinctly different from that of the distal fluxes. Second, the chemistry of the waters at each bank station along the archipelago was characterized and compared with the chemistry of the distal waters to determine if differences in the particle flux were reflected in the carbon chemistry. Higher alkalinity and carbonate ion concentrations were observed around all of the banks studied. The saturation state of these waters suggests that the dissolution of some magnesian calcite and aragonite phases could explain the higher alkalinity values. Calculations suggest that the dissolution of benthically-derived aragonite and magnesian calcite may be an important component of the North Pacific alkalinity budget and a potential sink for anthropogenic CO2.  相似文献   
113.
Comprehensive GC/MS analysis was applied to both the mobile liquid phase (seepage water) and the immobile solid matter of discrete layers derived from a waste deposit landfill. The vertical distribution of organic compounds supports information on the transport, transfer and transformation processes with depth and, consequently, with time.Numerous low molecular weight organic contaminants of natural and xenobiotic origin were identified and partially quantified. Several were selected to act as molecular indicators for different processes. Interpretation of their occurrence and concentration profiles (considering possible waste sources) and their molecular properties allowed us to (i) differentiate immobile and mobile fractions, (ii) reveal restrictions in the vertical transport by transfer processes between particulate and water phase, (iii) identify dynamic accumulations of individual contaminants and (iv) estimate approximate residence times. In addition, intensive degradation processes were pointed out for the natural fraction of the organic matter by way of determination of specific transformation products. Besides the transformation of natural components, transformation of numerous xenobiotics was recognised. In particular, with respect to an important group of contaminants, the phthalate-based plasticisers, a detailed view of (i) the influence of transfer and transport phenomena on transformation processes as well as (ii) the consecutive appearance of different degradation steps in both seepage water and solid waste was pointed out. The information provides a valuable base for the prediction of the long term behaviour of organic contaminants in waste deposit landfills.  相似文献   
114.
115.
The constant capacitance model, a chemical surface complexation model, was applied to selenite, Se(IV), adsorption on 36 soils selected for variation in soil chemical properties. The constant capacitance model was able to fit Se(IV) adsorption by optimizing one monodentate Se(IV) surface complexation constant and the surface protonation constant. A general regression model was developed for predicting these surface complexation constants for Se(IV) from easily measured soil chemical characteristics. These chemical properties were inorganic carbon content, organic carbon content, iron oxide content, aluminum oxide content, and surface area. The prediction equations were used to obtain values for the surface complexation constants for four additional soils, thereby providing a completely independent evaluation of the ability of the constant capacitance model to describe Se(IV) adsorption. The model’s ability to predict Se(IV) adsorption was quantitative on one soil and semi-quantitative on three soils. Incorporation of these prediction equations into chemical speciation-transport models will allow simulation of soil solution Se(IV) concentrations under diverse non-calcareous agricultural and environmental conditions without the requirement of soil specific adsorption data and subsequent parameter optimization.  相似文献   
116.
Due to a lack of visible tephras in the Dead Sea record, this unique palaeoenvironmental archive is largely unconnected to the well-established Mediterranean tephrostratigraphy. Here we present first results of the ongoing search for cryptotephras in the International Continental Drilling Program (ICDP) sediment core from the deep Dead Sea basin. This study focusses on the Lateglacial (~15–11.4 cal. ka BP), when Lake Lisan – the precursor of the Dead Sea – shrank from its glacial highstand to the Holocene low levels. We developed a glass shard separation protocol and counting procedure that is adapted to the extreme salinity and sediment recycling of the Dead Sea. Cryptotephra is abundant in the Dead Sea record (up to ~100 shards cm-3), but often glasses are physically and/or chemically altered. Six glass samples from five tephra horizons reveal a heterogeneous geochemical composition, with mainly rhyolitic and some trachytic glasses potentially sourced from Italian, Aegean and Anatolian volcanoes. Most shards likely originate from the eastern Anatolian volcanic province and can be correlated using major element analyses with tephra deposits from swarm eruptions of the Süphan Volcano ~13 ka BP and with ashes from Nemrut Volcano, presumably the Lake Van V-16 volcanic layer at ~13.8 ka BP. In addition to glasses that match the TM-10-1 from Lago Grande di Monticchio (15 820±790 cal. a BP) tentatively correlated with the St. Angelo Tuff of Ischia, we further identified a cryptotephra with glass analyses which are chemically identical with those of the PhT1 tephra in the Philippon peat record (13.9–10.5 ka BP), and also a compositional match for the glass analyses of the Santorini Cape Riva Tephra (Y-2 marine tephra, 22 024±642 cal. a BP). These first results demonstrate the great potential of cryptotephrochronology in the Dead Sea record for improving its chronology and connecting the Levantine region to the Mediterranean tephra framework.  相似文献   
117.
This paper addresses the question of how spatial variability in the hydraulic and chemical properties of groundwater systems affects the transport and sorption behavior of pollutants at the field scale. In this paper, we limit our investigations on pollutants that adsorb according to an equilibrium controlled nonlinear Freundlich sorption isotherm. The new contribution of this paper is take into account not only spatially variable Freundlich distribution coefficients KSKS but spatially variable Freundlich nonlinearity parameters p as well. Using a homogenization theory approach, we shortly review the impact of spatially variable hydraulic properties on the transport and extend the theory to spatially variable chemical properties. We show that spatially variable Freundlich exponents cause a very different field scale transport and sorption behavior than spatial variations in the distribution coefficients only since in the first case field scale Freundlich parameters and field scale dispersion coefficients become concentration dependent. In particular, field scale retardation is much larger than small-scale retardation.  相似文献   
118.
The presence of outer stably stratified layers in planetary cores has been suggested for Earth, Saturn and Mercury. In this study, we use a 3-D numerical dynamo model to investigate the effects of a thin stable layer surrounding a convecting interior on the produced magnetic field. We find that a stable layer can destabilize the field morphology through a thermal wind that produces unfavorable zonal flows throughout the core. The direction of these zonal flows is prograde in equatorial regions, unlike a model with no stable layer that has retrograde equatorial flows. Our models therefore suggest that the Earth does not have a stable layer since we observe a westward drift as opposed to an eastward drift. For Saturn, we find that due to coupling of the flows in the stable and unstable layers, the layer does not act to shear out the non-axisymmetry in the observed magnetic field, and therefore cannot explain Saturn’s axisymmetric magnetic field. For Mercury, we find that if the stable layer is thin, it can actively produce strong or weak surface fields and not necessarily attenuate smaller scale features through the skin effect.  相似文献   
119.
In many studies, the distribution of soil attributes depends on both spatial location and environmental factors, and prediction and process identification are performed using existing methods such as kriging. However, it is often too restrictive to model soil attributes as dependent on a known, parametric function of environmental factors, which kriging typically assumes. This paper investigates a semiparametric approach for identifying and modeling the nonlinear relationships of spatially dependent soil constituent levels with environmental variables and obtaining point and interval predictions over a spatial region. Frequentist and Bayesian versions of the proposed method are applied to measured soil nitrogen levels throughout Florida, USA and are compared to competing models, including frequentist and Bayesian kriging, based an array of point and interval measures of out-of-sample forecast quality. The semiparametric models outperformed competing models in all cases. Bayesian semiparametric models yielded the best predictive results and provided empirical coverage probability nearly equal to nominal.  相似文献   
120.
Transverse dispersion, or tracer spreading orthogonal to the mean flow direction, which is relevant e.g, for quantifying bio-degradation of contaminant plumes or mixing of reactive solutes, has been studied in the literature less than the longitudinal one. Inferring transverse dispersion coefficients from field experiments is a difficult and error-prone task, requiring a spatial resolution of solute plumes which is not easily achievable in applications. In absence of field data, it is a questionable common practice to set transverse dispersivities as a fraction of the longitudinal one, with the ratio 1/10 being the most prevalent. We collected estimates of field-scale transverse dispersivities from existing publications and explored possible scale relationships as guidance criteria for applications. Our investigation showed that a large number of estimates available in the literature are of low reliability and should be discarded from further analysis. The remaining reliable estimates are formation-specific, span three orders of magnitude and do not show any clear scale-dependence on the plume traveled distance. The ratios with the longitudinal dispersivity are also site specific and vary widely. The reliability of transverse dispersivities depends significantly on the type of field experiment and method of data analysis. In applications where transverse dispersion plays a significant role, inference of transverse dispersivities should be part of site characterization with the transverse dispersivity estimated as an independent parameter rather than related heuristically to longitudinal dispersivity.  相似文献   
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