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1.
We present the preliminary results of a study of how small stellar systems merge to form larger ones. As we display the families of galaxies in the μe - Re plane (effective surface brightness versus effective radius) we realize that different morphological types occupy different loci, evidencing the different physical mechanisms operating in each family. As proposed by Capaccioli et al. (1992) this diagram is the logical equivalent of the HR diagram for stars. Here we take some initial steps in understanding of how we can establish the evolutionary tracks, solely due to dynamical processes, in the μe - Re plane, ultimately making a dwarf elliptical to turn into a normal elliptical galaxy. This revised version was published online in August 2006 with corrections to the Cover Date.  相似文献   
2.
Abstract— The mineral compositions of 250 micrometeorites have been studied and olivines and low-calcium pyroxenes with crystals larger than 5 μm have been analyzed. While magnesium-rich grains dominate, the Fa content of olivine may reach 50% and the Fs content of pyroxene may reach 26%. The Ca and Mn of the olivine show no consistent trends with increasing Fe, but Cr shows a negative correlation. For low-Ca pyroxene, Al and Cr contents are generally higher than in pyroxenes of equilibrated chondrites but similar to those of highly unequilibrated chondrites. Calcium-bearing pyroxene, feldspar and chromite are rare in the micrometeorites which were selected because of their high Mg, Si, Fe and their low Ca and Al content. All these minerals are found as coarse-grained particles often with adhering iron-rich scoria or as clasts in fine-grained or scoriaceous micrometeorites. Apart from a few particles which could be the debris of ordinary chondrites, most micrometeorites probably come from a common source similar, but not identical to carbonaceous chondrites, as shown by their lower Ni and S content and their different oxygen isotopic composition assuming two measurements performed on olivine grains prove to be typical.  相似文献   
3.
Abstract— Platinum group elements (PGE) enrichments are found in Fe-Ni blebs (<1 μm) in Al- and Cr-rich objects in the ordinary chondrites Ste. Marguerite, Forest Vale, Montferré. In Ste. Marguerite, high ZrO2 concentrations (baddeleyite) are also present in a chromite inclusion. Iridium enrichment in this material compared to its metal content is confirmed by INAA. The widespread occurrence of PGE in Al- and Cr-rich objects, mostly present in H-group chondrites of nearly equilibrated types, must be taken into account to understand their conditions of formation.  相似文献   
4.
Abstract Dahmani is a shocked LL6 fragmental breccia. According to the composition of the silicates (olivine Fa30,32.6, orthopyroxene Fs24.5–26.3) and of the metal (a 60% Ni taenite) it is one of the most oxidised known.  相似文献   
5.
Seventy-seven gem opals from ten countries were analyzed by inductively coupled plasma-mass spectrometry (ICP-MS) through a dilution process, in order to establish the nature of the impurities. The results are correlated to the mode of formation and physical properties and are instrumental in establishing the geographical origin of a gem opal. The geochemistry of an opal is shown to be dependant mostly on the host rock, at least for examples from Mexico and Brazil, even if modified by weathering processes. In order of decreasing concentration, the main impurities present are Al, Ca, Fe, K, Na, and Mg (more than 500 ppm). Other noticeable elements in lesser amounts are Ba, followed by Zr, Sr, Rb, U, and Pb. For the first time, geochemistry helps to discriminate some varieties of opals. The Ba content, as well as the chondrite-normalized REE pattern, are the keys to separating sedimentary opals (Ba > 110 ppm, Eu and Ce anomalies) from volcanic opals (Ba < 110 ppm, no Eu or Ce anomaly). The Ca content, and to a lesser extent that of Mg, Al, K and Nb, helps to distinguish gem opals from different volcanic environments. The limited range of concentrations for all elements in precious (play-of-color) compared to common opals, indicates that this variety must have very specific, or more restricted, conditions of formation. We tentatively interpreted the presence of impurities in terms of crystallochemistry, even if opal is a poorly crystallized or amorphous material. The main replacement is the substitution of Si4+ by Al3+ and Fe3+. The induced charge imbalance is compensated chiefly by Ca2+, Mg2+, Mn2+, Ba2+, K+, and Na+. In terms of origin of color, greater concentrations of iron induce darker colors (from yellow to “chocolate brown”). This element inhibits luminescence for concentrations above 1000 ppm, whereas already a low content in U (≤ 1 ppm) induces a green luminescence.  相似文献   
6.
Magnesium and strontium isotope signatures were determined during different seasons for the main rivers of the Moselle basin, northeastern France. This small basin is remarkable for its well-constrained and varied lithology on a small distance scale, and this is reflected in river water Sr isotope compositions. Upstream, where the Moselle River drains silicate rocks of the Vosges mountains, waters are characterized by relatively high 87Sr/86Sr ratios (0.7128-0.7174). In contrast, downstream of the city of Epinal where the Moselle River flows through carbonates and evaporites of the Lorraine plateau, 87Sr/86Sr ratios are lower, down to 0.70824.Magnesium in river waters draining silicates is systematically depleted in heavy isotopes (δ26Mg values range from −1.2 to −0.7‰) relative to the value presently estimated for the continental crust and a local diorite (−0.5‰). In comparison, δ26Mg values measured in soil samples are higher (∼0.0‰). This suggests that Mg isotope fractionation occurs during mineral leaching and/or formation of secondary clay minerals. On the Lorraine plateau, tributaries draining marls, carbonates and evaporites are characterized by low Ca/Mg (1.5-3.2) and low Ca/Sr (80-400) when compared to local carbonate rocks (Ca/Mg = 29-59; Ca/Sr = 370-2200), similar to other rivers draining carbonates. The most likely cause of the Mg and Sr excesses in these rivers is early thermodynamic saturation of groundwater with calcite relative to magnesite and strontianite as groundwater chemistry progressively evolves in the aquifer. δ26Mg of the dissolved phases of tributaries draining mainly carbonates and evaporites are relatively low and constant throughout the year (from −1.4‰ to −1.6‰ and from −1.2‰ to −1.4‰, respectively), within the range defined for the underlying rocks. Downstream of Epinal, the compositions of the Moselle River samples in a δ26Mg vs. 87Sr/86Sr diagram can be explained by mixing curves between silicate, carbonate and evaporite waters, with a significant contribution from the Vosgian silicate lithologies (>70%). Temporal co-variation between δ26Mg and 87Sr/86Sr for the Moselle River throughout year is also observed, and is consistent with a higher contribution from the Vosges mountains in winter, in terms of runoff and dissolved element flux. Overall, this study shows that Mg isotopes measured in waters, rocks and soils, coupled with other tracers such as Sr isotopes, could be used to better constrain riverine Mg sources, particularly if analytical uncertainties in Mg isotope measurements can be improved in order to perform more precise quantifications.  相似文献   
7.
Seawater samples were collected in the lagoon of Nouméa (southwest New Caledonia) along two transects from eutrophic coastal bays to the oligotrophic barrier reef. Land-based emissions to the lagoon were measured with dissolved and particulate concentrations of chromium (Cr) and nickel (Ni), used as tracers of both terrigenous and industrial (Ni ore treatment) activities, as well as dissolved and particulate concentrations of zinc (Zn), used as a tracer of urban effluents. The spatial variability of metal concentrations was related to geochemical and hydrodynamic conditions, i.e., respectively: (1) natural and anthropogenic emission sources, and chemical processes occurring in the water column; and (2) water residence times. The parameter used to describe the residence time of water masses was the local e-flushing time, i.e. the time required for a tracer mass contained within a given station to be reduced by a factor 1/e. High metal concentrations were found in coastal areas (up to 9000 ng dissolved Ni L−1), and steeply decreased with distance from the coast (down to 101 ng dissolved Ni L−1 near the barrier reef) to reach levels similar to those found in remote Pacific waters, suggesting a rapid renewal of waters close to the barrier. Distributions of metals in the lagoon are controlled upstream by land-based emission sources and later chemical processes. Then hydrodynamics constrain metal distributions, as shown by the observed relationship between local e-flushing times and the spatial variability of metal concentrations. In addition, a change in the direction of prevailing winds yielded a decrease of dissolved metal concentrations at the same site by a factor of 2.5 (Cr and Ni) and 2.9 (Zn). It is suggested that the residence time is a key parameter in the control of elemental concentrations in the lagoon waters, as much as land-based emission sources.  相似文献   
8.
We present new sea-level data from the coasts of southern Tunisia, between the Gulf of Gabès and the Libyan border. The work tests, previously, published evidence on Holocene shorelines, and confirmed that a distinct emergence has occurred in this area during this time. The emergence peak lies at least 186 ± 11 cm above present and is inferred from: (1) AMS radiocarbon dates of subtidal vermetids and boring shells collected in growth position, and (2) careful assessment of tidal heights. Maximum emergence took place between about 6000 and 5000 14C years BP; it cannot be ascribed to tectonics and is probably related to post-glacial hydro-isostatic effects. It challenges the inference of a 3-m global sea-level rise since 6000 years BP due to residual Antarctic melting.  相似文献   
9.
Since a state law issued in 1989, every big town in Colombia has to promote its own preparedness programme for disaster relief in the framework of the Oficina Nacional para la Atencion de Desastres (1987). Such a programme includes a very detailed hazard-zone map for flooding and debris flows in the densely inhabited suburbs of Ibagué city (capital of Tolima Department), as well as enquiries about risk knowledge and consciousness among people who live at high risk. We stress the fact that both detailed hazard-zone maps and enquiries should be closely undertaken at the same time, and that distinguishing previous knowledge, existing consciousness and risk perception to forecast the behaviour of people and of the community in case of disaster, are criteria for a better risk assessment.  相似文献   
10.
Summary Geochemical characteristics were systematically determined for Early Cretaceous samples of carbonatitic rocks from Eastern Paraguay (Rio Apa, Amambay and Central Provinces). The data show that all the occurrences have an enriched isotopic signature and that the carbonatites have negligible or absent crustal signature. A petrogenetic model (parent liquids, fractional crystallization, hydrothermal interactions and weathering) is proposed as a function of incompatible trace element, stable (O-C) and radiogenic (Sr-Nd) isotope variations with the aim to test the significance of carbonatitic complexes as a marker of the metasomatized subcontinental lithospheric mantle. The results indicate that the carbonatites and primary carbonates from eastern Paraguay, and those from the north eastern Paraná Basin (SE Brazil), were affected by metasomatic events distinct in time and composition.
Karbonatite aus Ost-Paraguay und ihre genetische Beziehung zu Kalium-Magmatismus: C O, Sr und Nd isotope
Zusammenfassung Die geochemischen Charakteristika von frühkretazischen Karbonatitproben aus Ostparaguay (Rio Alpa, Amambay und Zentrale Provinzen) wurden untersucht. Die Daten belegen, daß alle Vorkommen eine isotopische Anreicherungssignatur zeigen und daß ihnen eine entsprechende Krustensignatur fehlt. Ein Petrologisches Modell (Ausgangsschmelze, fraktionierte Kristallisation, hydrothermale Interaktion und Verwitterung) wird auf Grund der Verteilung der inkompatiblen Spurenelemente, der stabilen (C-O) und radiogenen (Sr-Nd) Isotope vorgeschlagen. Es versucht die Bedeutung der Karbonatitkomplexe als Markerhorizonte des metasomatischen subkontinentalen Mantels zu überprüfen. Die Ergebnisse zeigen, daß die Karbonatite und die primären Karbonate in Ostparaguay, und jene aus dem Paraná Becken SüdostBrasiliens durch zeitlich und zusammensetzungsmäßig unterschiedliche metasomatische Prozesse erfaßt wurden.


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