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181.
J. L. Simón M. A. Soriano L. E. Arlegui J. Gracia C. L. Liesa A. Pocoví 《Environmental Geology》2008,53(5):1057-1065
Space and time variations of alluvial karst subsidence in the central Ebro Basin are analysed in trenches (paleodolines),
aerial photographs (historical dolines) and field surveys (present-day active dolines). The measured subsidence rates, as
well as a comparison between densities of paleodolines computed in randomly selected scan-lines and density of active dolines
computed in maps, suggest that present-day subsidence in favourable areas is more intense than that of Pleistocene times.
According to diachronic maps drawn from (a) different aerial photographs taken after 1946 and (b) field surveys on deformations
in urbanized areas, subsidence behaved as a nearly steady process while the whole area was used for agriculture. In contrast,
rapid changes (through periods of several tens of years) have occurred in urbanized areas, in which dolines expand their boundaries
through small marginal collapses, shifting sharply their sinking centres to neighbouring sites. These rapid changes do not
have an equivalent in observed paleodolines. 相似文献
182.
This work deals with disposal of slurries generated during the cutting and polishing processes of slabs of decorative sedimentary
carbonate rocks in the north western Sicily. At present, they are used as fillers of dismantled quarries near the sawmills
and, as a final step of reclamation, are covered with earth layers. In spite of such inexpensive solution, there is lack of
knowledge about the composition of the waste. In order to assess if there is any threat for the environment and to suggest
indications for alternative solutions, such as recycling or inactivation processes, the slurries were analysed by XR diffraction,
simultaneous thermal analysis, ICP/MS, ionic chromatography, FTIR, UV-Vis, COD and TOC measurements, grain size analysis.
Results indicate that the slurries can threaten the groundwater, because of the high chemical oxygen demand; furthermore they
can modify the mechanism of groundwater recharge, because of their grain size distribution. Some laboratory tests show that,
even in very aggressive conditions, the solid pollutants persist in the waste and slowly release into water the products of
their degradation. The slurry therefore should be subjected to inactivation treatment before disposal or, alternatively, recycled
as secondary raw material for a suitable process. 相似文献
183.
The Hill Country of Central Texas, USA, is undergoing rapid socioeconomic development, but environmental management of this
region is hampered by misconceptions about local bedrock, soils, terrain, and hydrologic processes. The Hill Country is underlain
mostly by Glen Rose Limestone (Lower Cretaceous) and exhibits a stepped terrain, which has been incorrectly attributed to
alternating hard and soft bedrock strata. Other characteristics mistakenly attributed to this landscape include thin soils
with scant water-retention capabilities, and rapid runoff as the dominant hydrologic process. This report presents new findings:
unweathered bedrock is well indurated, but interbeds exhibit variable weathering rates. Recessive slopes (“risers”) on this
stepped terrain result from rapid deterioration of strata having generally heterogeneous depositional fabrics (bioturbation
and irregular clay partings) in contrast to ledge-forming strata having homogeneous fabrics. A stony regolith is thus formed
beneath risers, providing porous and permeable ground that retards runoff and promotes the formation of moderately deep to
deep (two-tiered) regolith/soil zones. These surficial materials on local steep slopes compose important natural environmental
buffers; they support diverse biota and enhanced geochemical cycling of nutrients; they also exhibit significant water retention
and enhanced erosion abatement. Proper land management demands recognition of these attributes in the siting, design, and
construction of facilities. 相似文献
184.
A new method of estimating the ratio between in situ rock stresses and tectonics based on empirical and probabilistic analyses 总被引:1,自引:0,他引:1
This paper describes a new procedure for assessing the ratio between in situ stresses in rock masses by means of K (K = σH / σv, being σH and σv principal stress) and tectonics for purposes of engineering geology and rock mechanics. The method combines the use of the logic decision tree and the empirical relationship between the Tectonic Stress Index, TSI, and a series of K in situ values obtained from an extensive database. The decision tree considers geological and geophysical factors affecting stress magnitudes both on the regional and local scale. The TSI index is defined by geological and geomechanical parameters. The method proposed provides an assessment of the magnitude of horizontal stresses of tectonic origin. Results for several regions of Europe are presented and the possible applications of the procedure are discussed. 相似文献
185.
Li-Sr-Nd isotope signatures of the plume and cratonic lithospheric mantle beneath the margin of the rifted Tanzanian craton (Labait) 总被引:3,自引:2,他引:1
Sonja Aulbach Roberta L. Rudnick William F. McDonough 《Contributions to Mineralogy and Petrology》2008,155(1):79-92
Lithium concentrations and isotopic compositions of olivine and 87Sr/86Sr and 143Nd/144Nd of coexisting clinopyroxene from peridotite xenoliths from the Quaternary Labait volcano, Tanzania, document the influence
of rift-related metasomatism on the ancient cratonic mantle. Olivines show negative correlations between Fo content and both
δ7Li and Li concentrations. Olivines in iron-rich peridotites (Fo85–87) have high Li concentrations (3.2–4.8 ppm) and heavy δ7Li (+5.2 to +6.6). In contrast, olivines in ancient, refractory peridotites have lower Li concentrations (∼2 ppm) and relatively
light δ7Li (+2.6 to +3.5). This reflects mixing between ancient, refractory cratonic lithosphere and asthenosphere-derived rift magmas.
A uniquely fertile, deformed, high-temperature garnet lherzolite, interpreted to be from the base of the lithosphere, has
a 87Sr/86Sr of 0.7029 and 143Nd/144Nd of 0.51286, similar to HIMU oceanic basalts. It provides the best estimate of the Sr–Nd isotope composition of the upwelling
mantle (i.e., plume, sensu lato) underlying this portion of the East African Rift, and is slightly less radiogenic compared
to previous estimates of the plume that were based on rift basalts. Although elevated δ7Li are not exclusive to HIMU source regions, the data collectively indicate that the plume beneath Labait has HIMU characteristics
in Sr, Nd and Li isotope composition.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
186.
The effects of metamorphism on O and Fe isotope compositions in the Biwabik Iron Formation, northern Minnesota 总被引:3,自引:0,他引:3
Elizabeth Valaas Hyslop John W. Valley Clark M. Johnson Brian L. Beard 《Contributions to Mineralogy and Petrology》2008,155(3):313-328
The Biwabik Iron Formation of Minnesota (1.9 Ga) underwent contact metamorphism by intrusion of the Duluth Complex (1.1 Ga).
Apparent quartz–magnetite oxygen isotope temperatures decrease from ∼700°C at the contact to ∼375°C at 2.6 km distance (normal
to the contact in 3D). Metamorphic pigeonite at the contact, however, indicates that peak temperatures were greater than 825°C.
The apparent O isotope temperatures, therefore, reflect cooling, and not peak metamorphic conditions. Magnetite was reset
in δ18O as a function of grain size, indicating that isotopic exchange was controlled by diffusion of oxygen in magnetite for samples
from above the grunerite isograd. Apparent quartz–magnetite O isotope temperatures are similar to calculated closure temperatures
for oxygen diffusion in magnetite at a cooling rate of ∼5.6°C/kyr, which suggests that the Biwabik Iron Formation cooled from
∼825 to 400°C in ∼75 kyr at the contact with the Duluth Complex. Isotopic exchange during metamorphism also occurred for Fe,
where magnetite–Fe silicate fractionations decrease with increasing metamorphic grade. Correlations between quartz–magnetite
O isotope fractionations and magnetite–iron silicate Fe isotope fractionations suggest that both reflect cooling, where the
closure temperature for Fe was higher than for O. The net effect of metamorphism on δ18O–δ56Fe variations in magnetite is a strong increase in δ18OMt and a mild decrease in δ56Fe with increasing metamorphic grade, relative to the isotopic compositions that are expected at the low temperatures of initial
magnetite formation. If metamorphism of Iron Formations occurs in a closed system, bulk O and Fe isotope compositions may
be preserved, although re-equilibration among the minerals may occur for both O and Fe isotopes.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
187.
David M. Sherman Caroline L. Peacock Christopher G. Hubbard 《Geochimica et cosmochimica acta》2008,72(2):298-310
Sorption of U(VI) to goethite is a fundamental control on the mobility of uranium in soil and groundwater. Here, we investigated the sorption of U on goethite using EXAFS spectroscopy, batch sorption experiments and DFT calculations of the energetics and structures of possible surface complexes. Based on EXAFS spectra, it has previously been proposed that U(VI), as the uranyl cation , sorbs to Fe oxide hydroxide phases by forming a bidentate edge-sharing (E2) surface complex, >Fe(OH)2UO2(H2O)n. Here, we argue that this complex alone cannot account for the sorption capacity of goethite (α-FeOOH). Moreover, we show that all of the EXAFS signal attributed to the E2 complex can be accounted for by multiple scattering. We propose that the dominant surface complex in CO2-free systems is a bidentate corner-sharing (C2) complex, (>FeOH)2UO2(H2O)3 which can form on the dominant {101} surface. However, in the presence of CO2, we find an enhancement of UO2 sorption at low pH and attribute this to a (>FeO)CO2UO2 ternary complex. With increasing pH, U(VI) desorbs by the formation of aqueous carbonate and hydroxyl complexes. However, this desorption is preceded by the formation of a second ternary surface complex (>FeOH)2UO2CO3. The three proposed surface complexes, (>FeOH)2UO2(H2O)3, >FeOCO2UO2, and (>FeOH)2UO2CO3 are consistent with EXAFS spectra. Using these complexes, we developed a surface complexation model for U on goethite with a 1-pK model for surface protonation, an extended Stern model for surface electrostatics and inclusion of all known UO2-OH-CO3 aqueous complexes in the current thermodynamic database. The model gives an excellent fit to our sorption experiments done in both ambient and reduced CO2 environments at surface loadings of 0.02-2.0 wt% U. 相似文献
188.
Atomistic simulations have been carried out to investigate the mechanisms of noble gas incorporation in minerals using both the traditional two-region approach and the “supercell” method. The traditional two-region approach has been used to calculate defect energies for Ne, Ar, Kr and Xe incorporation in MgO, CaO, diopside and forsterite in the static limit and at one atmosphere pressure. The possibilities of noble gas incorporation via both substitution and interstitial mechanisms are studied. The favored mechanism varies from mineral to mineral and from noble gas to noble gas. In all minerals studied, the variation of the solution energies of noble gas substitution with atomic radius appears approximately parabolic, analogous to those for 1+, 2+, 3+ and 4+ trace element incorporation on crystal lattice sites. Noble gas solution energies thus also fall on a curve, similar to those previously observed for cations with different charges, but with much lower curvature.The “supercell” method has been used to investigate the pressure dependence of noble gas incorporation in the same systems. Results indicate a large variation of the solubility of the larger noble gases, Kr and Xe with pressure. In addition, explicit simulation of incorporation at the (0 0 1) surface of MgO shows that the solubility of the heavier noble gases may be considerably enhanced by the presence of interfaces. 相似文献
189.
Nancy L. Chabot Andrew J. Campbell David S. Draper Munir Humayun Elizabeth Cottrell 《Geochimica et cosmochimica acta》2008,72(16):4146-4158
Earth’s core may contain C, and it has been suggested that C in the core could stabilize the formation of a solid inner core composed of Fe3C. We experimentally examined the Fe-C system at a pressure of 5 GPa and determined the Fe-C phase diagram at this pressure. In addition, we measured solid metal/liquid metal partition coefficients for 17 trace elements and examined the partitioning behavior between Fe3C and liquid metal for 14 trace elements. Solid metal/liquid metal partition coefficients are similar to those found in one atmosphere studies, indicating that the effect of pressure to 5 GPa is negligible. All measured Fe3C/liquid metal partition coefficients investigated are less than one, such that all trace elements prefer the C-rich liquid to Fe3C. Fe3C/liquid metal partition coefficients tend to decrease with decreasing atomic radii within a given period. Of particular interest, our 5 GPa Fe-C phase diagram does not show any evidence that the Fe-Fe3C eutectic composition shifts to lower C contents with increasing pressure, which is central to the previous reasoning that the inner core may be composed of Fe3C. 相似文献
190.
Martin R. Lee Mark E. Hodson Maureen MacKenzie Caroline L. Smith 《Geochimica et cosmochimica acta》2008,72(20):4962-4975
Our ability to identify thin non-stoichiometric and amorphous layers beneath mineral surfaces has been tested by undertaking X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM) work on alkali feldspars from pH 1 dissolution experiments. The outcomes of this work were used to help interpret XPS and TEM results from alkali feldspars weathered for <10,000 years in soils overlying the Shap Granite (north-west England). The chemistry of effluent solutions indicates that silica-rich layers a few nanometers in thickness formed during the pH 1 experiments. These layers can be successfully identified by XPS and have lower Al/Si, Na/Si, K/Si and Ca/Si values than the outermost ∼9 nm of unweathered controls. Development of Al-Si non-stoichiometry is coupled with loss of crystal structure to produce amorphous layers that are identifiable by TEM where >∼2.5 nm thick, whereas the crystallinity of albite is retained despite leaching of Na to depths of tens to hundreds on nanometers. Integration of XPS data over the outermost 6-9 nm of naturally weathered Shap feldspars shows that they have stoichiometric Al/Si and K/Si ratios, which is consistent with findings of previous TEM work on the same material that they lack amorphous layers. There is some XPS evidence for loss of K from the outermost couple of nanometers of Shap orthoclase, and the possibility of leaching of Na from albite to greater depths cannot be excluded using the XPS or TEM results. This study demonstrates that the leached layer model, as formulated from laboratory experiments, is inapplicable to the weathering of alkali feldspars within acidic soils, which is an essentially stoichiometric reaction. 相似文献