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1.
Carlos J.A.P. Martins 《Astrophysics and Space Science》2003,283(4):439-444
I briefly present the Organizing Committee's and my own motivation for organizing this workshop, and I suggest a few key questions
for which we will try to find possible answers in the coming days.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
2.
C.A. Mendoza-Briceño 《Astrophysics and Space Science》1997,256(1-2):387-392
The thermal evolution of structures is investigated for different values of the size of structure. A simplified cooling function and a constant heating mechanism are assumed. Analytical criteria for thermal instability are obtained. It is found that the response of the thermal structure not only depends on the amplitude of the disturbances, but also on whether the disturbance increases or decreases the initial steady temperature. Additionally, the evolution of the structure is examined numerically by using a time-dependent code under the assumption that the inertia terms are small. In particular, the analytical criteria obtained for thermal instability are verified. 相似文献
3.
4.
Larisa A. Yakovina Yakiv V. Pavlenko Carlos Abia 《Astrophysics and Space Science》2003,288(3):279-286
Lithium abundances in the atmospheres of the super Li-rich C-giants WZ Cas and WX Cyg are derived by the spectral synthesis
technique using the Li I resonance line at λ670.8 nm and three subordinate lines at λλ 812.6, 610.4 and 497.2 nm. The differences
between the Li abundances derived from the λ670.8 nm line and the λλ 497.2, 812.6 nm lines do not exceed ±0.5 dex. The lithium
line at λ610.4 nm provides typically lower abundances than the resonance line (by ≈ 1 dex). The mean LTE and NLTE Li abundances
from three Li I lines (excluding λ610.4 nm) are 4.7, 4.9 for WZ Cas, and 4.6, 4.8 for WX Cyg, respectively.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
5.
Miguel Cerviño 《Astrophysics and Space Science》2003,284(2):897-900
Evolutionary synthesis models have been used to study the physical properties of unresolved populations in a wide range of
scenarios. Unfortunately, their self-consistency is difficult to test and there are some theoretical open questions without
an answer: (1) The change of the homology relations assumed in the computation of isochrones due to the effect of stellar
winds (or rotation) and the discontinuities in the stellar evolution are not considered. (2) There is no consensus about how
the isochrones must be integrated. (3) The discreteness of the stellar populations (that produce an intrinsic statistical
dispersion) usually are not taken into account, and model results are interpreted in a deterministic way instead of a statistical
one. The objective of this contribution is to present some inconsistencies in the computation and some cautions in the application
of the results of such codes.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
6.
Verónica Oliveros Gilbert Féraud Luis Aguirre Luis Ramírez Michel Fornari Carlos Palacios Miguel Parada 《Mineralium Deposita》2008,43(3):281-293
The 40Ar/39Ar geochronological method was applied to date magmatic and hydrothermal alteration events in the Mantos Blancos mining district
in the Coastal Cordillera of northern Chile, allowing the distinction of two separate mineralization events. The Late Jurassic
Mantos Blancos orebody, hosted in Jurassic volcanic rocks, is a magmatic-hydrothermal breccia-style Cu deposit. Two superimposed
mineralization events have been recently proposed. The first event is accompanied by a phyllic hydrothermal alteration affecting
a rhyolitic dome. The second mineralization event is related to the intrusion of bimodal stocks and sills inside the deposit.
Because of the superposition of several magmatic and hydrothermal events, the obtained 40Ar/39Ar age data are complex; however, with a careful interpretation of the age spectra, it is possible to detect complex histories
of successive emplacement, alteration, mineralization, and thermal resetting. The extrusion of Jurassic basic to intermediate
volcanic rocks of the La Negra Formation is dated at 156.3 ± 1.4 Ma (2σ) using plagioclase from an andesitic lava flow. The first mineralization event and associated phyllic alteration affecting
the rhyolitic dome occurred around 155–156 Ma. A younger bimodal intrusive event, supposed to be equivalent to the bimodal
stock and sill system inside the deposit, is probably responsible for the second mineralization event dated at ca. 142 Ma.
Other low-temperature alteration events have been dated on sericitized plagioclase at ca. 145–146, 125, and 101 Ma. This is
the first time that two distinct mineralization events have been documented from radiometric data for a copper deposit in
the metallogenic belt of the Coastal Cordillera of northern Chile.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
7.
8.
Reactive dissolved Hg (HgR), non-reactive dissolved Hg (HgNR), particulate Hg (HgP), dissolved organic C (DOC), particulate organic C (POC), salinity and other interpretative parameters were determined in water samples collected in the North Channel and in adjacent areas of the Tagus estuary (Portugal). Higher concentrations of both dissolved and particulate Hg in the North Channel indicate a pollution source and raise the possibility of Hg escaping to adjacent areas by tidal action. This transport was confirmed by the increase of HgR with salinity and HgNR with DOC, along a longitudinal axis paralleling the North Channel. Apparently, Hg leaving this channel is progressively complexed by inorganic and organic ligands. Near the mouth of the estuary, values decreased reflecting dilution with seawater. Moreover the HgP:POC ratio also increased seaward, suggesting mixing with Hg enriched particles that escaped the North Channel, or incorporation of dissolved Hg species in river-derived particles. These results suggest that the pathway of anthropogenic Hg in contaminated waters may be identified by their enrichment in organic matter, both in the dissolved and particulate fraction. 相似文献
9.
Jos M. Marques Paula M. Carreira Maria Rosrio Carvalho Maria J. Matias Fraser E. Goff Maria J. Basto Rui C. Graa Luís Aires-Barros Luís Rocha 《Applied Geochemistry》2008,23(12):3278-3289
This paper reviews the geochemical, isotopic (2H, 18O, 13C, 3H and 14C) and numerical modelling approaches to evaluate possible geological sources of the high pH (11.5)/Na–Cl/Ca–OH mineral waters from the Cabeço de Vide region (Central-Portugal). Water–rock interaction studies have greatly contributed to a conceptual hydrogeological circulation model of the Cabeço de Vide mineral waters, which was corroborated by numerical modelling approaches. The local shallow groundwaters belong to the Mg–HCO3 type, and are derived by interaction with the local serpentinized rocks. At depth, these type waters evolve into the high pH/Na–Cl/Ca–OH mineral waters of Cabeço de Vide spas, issuing from the intrusive contact between mafic/ultramafic rocks and an older carbonate sequence. The Cabeço de Vide mineral waters are supersaturated with respect to serpentine indicating that they may cause serpentinization. Magnesium silicate phases (brucite and serpentine) seem to control Mg concentrations in Cabeço de Vide mineral waters. Similar δ2H and δ18O suggest a common meteoric origin and that the Mg–HCO3 type waters have evolved towards Cabeço de Vide mineral waters. The reaction path simulations show that the progressive evolution of the Ca–HCO3 to Mg–HCO3 waters can be attributed to the interaction of meteoric waters with serpentinites. The sequential dissolution at CO2 (g) closed system conditions leads to the precipitation of calcite, magnesite, amorphous silica, chrysotile and brucite, indicating that the waters would be responsible for the serpentinization of fresh ultramafic rocks (dunites) present at depth. The apparent age of Cabeço de Vide mineral waters was determined as 2790 ± 40 a BP, on the basis of 14C and 13C values, which is in agreement with the 3H concentrations being below the detection limit. 相似文献
10.
The passivation of calcite by acid mine water. Column experiments with ferric sulfate and ferric chloride solutions at pH 2 总被引:2,自引:1,他引:1
Josep M. Soler Marco Boi Jos Luis Mogolln Jordi Cama Carlos Ayora Peter S. Nico Nobumichi Tamura Martin Kunz 《Applied Geochemistry》2008,23(12):3579-3588
Column experiments, simulating the behavior of passive treatment systems for acid mine drainage, have been performed. Acid solutions (HCl or H2SO4, pH 2), with initial concentrations of Fe(III) ranging from 250 to 1500 mg L−1, were injected into column reactors packed with calcite grains at a constant flow rate. The composition of the solutions was monitored during the experiments. At the end of the experiments (passivation of the columns), the composition and structure of the solids were measured. The dissolution of calcite in the columns caused an increase in pH and the release of Ca into the solution, leading to the precipitation of gypsum and Fe–oxyhydroxysulfates (Fe(III)–SO4–H+ solutions) or Fe–oxyhydroxychlorides (Fe(III)–Cl–H+ solutions). The columns worked as an efficient barrier for some time, increasing the pH of the circulating solutions from 2 to 6–7 and removing its metal content. However, after some time (several weeks, depending on the conditions), the columns became chemically inert. The results showed that passivation time increased with decreasing anion and metal content of the solutions. Gypsum was the phase responsible for the passivation of calcite in the experiments with Fe(III)–SO4–H+ solutions. Schwertmannite and goethite appeared as the Fe(III) secondary phases in those experiments. Akaganeite was the phase responsible for the passivation of the system in the experiments with Fe(III)–Cl–H+ solutions. 相似文献