The evolutionary history of early-type galaxies as derived from the fundamental plane     

M.A. Pahre  S.G. Djorgovski  R.R. De Carvalho 《Astrophysics and Space Science》2001,276(2-4):983-990

The fundamental plane (FP) scaling relations and their evolution are a powerful tool for studying the global properties of early-type galaxies and their evolutionary history. The form of the FP, as derived by surveys in the local Universe at wavelengths ranging from the U to the K band, cannot be explained by metallicity variations alone among early-type galaxies; systematic variations in age, dark matter content, or homology breaking are required. A large-scale study of early-type galaxies at 0.1 < z < 0.6demonstrates that the SB intercept of the FP, the rest frame (U-V) colour, and the absorption line strengths all evolve passively, thereby implying a high mean formation redshift for the stellar content. The slope of the FP evolves with redshift, which is broadly consistent with systematic age effects occurring along the early-type galaxy sequence. The implication that the least luminous early-type galaxies formed later than the luminous galaxies is discussed in the context of the evolution of thecolour–magnitude relation, the Butcher–Oemler effect and hierarchical galaxy formation models. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

Envelopes of rapidly rotating neutron stars     

D. De Niem  U. Geppert  H. -J. Wiebicke 《Astrophysics and Space Science》1985,110(2):331-336

Motivated by the discovery of the millisecond pulsars, we consider the effect of rapid rotation on the envelope of a neutron star. Solving the equation of hydrostatic equilibrium we find expressions for the density and oblateness as functions of radius and polar angle.  相似文献   

Poisson-distributed patterns of explosive eruptive activity   总被引：1，自引：0，他引：1  

Servando De la Cruz-Reyna 《Bulletin of Volcanology》1991,54(1):57-67

The study of patterns of eruption occurrence could lead to a better understanding of the physics behind the volcanic process. However, various attempts to find a single statistical distribution that describes the occurrences of volcanic eruptions have not been successful. Global data show that, if the energies of point events in time (eruptions) are properly accounted above a certain noise level, the stochastic process — whose realization consists of explosive volcanic events — can be well represened by a Poisson point process, though not necessarily stationary. Many previous attempts to describe patterns of eruption occurrences were hampered by counting events with all levels of explosivity in the same category. When eruptions are separated by their sizes, the occurrence patterns of the higher magnitude eruptions become clearly Poissonian. In this study eruptions are classified by size using the Volcanic Explosivity Index (Newhall and Self 1982). Further analysis of the magnitude-characterized eruption data shows direct relations among the energy of eruptions, mean rate of occurrences and distribution of repose intervals between eruptions. An important result from the analysis of energy and mean rate of occurrence data is that, for global data, the product of those parameters is a constant. Simple load-and-discharge models provide an explanation of the random features of the volcanic processes. These considerations lead to the definition of a constinuous magnitude scale for volcanic eruptions which can consistently measure the energy and the rate-of-occurrence of eruptions over a wide range of values.  相似文献   

Crustal and upper mantle structures of the brazilian coast     

Jorge Luis De Souza 《Pure and Applied Geophysics》1991,136(2-3):245-264

The Rayleigh wave phase and group velocities in the period range of 24–39 sec, obtained from two earthquakes which occurred in northeastern brazil and which were recorded by the Brazilian seismological station RDJ (Rio de Janeiro), have been used to study crustal and upper mantle structures of the Brazilian coastal region. Three crustal and upper mantle models have been tried out to explain crustal and upper mantle structures of the region. The upper crust has not been resolved, due basically to the narrow period range of the phase and group velocities data. The phase velocity inversions have exhibited good resolutions for both lower crust and upper mantle, with shear wave velocities characteristic of these regions. The group velocity data inversions for these models have showed good results only for the lower crust. The shear wave velocities of the lower crust (3.86 and 3.89 km/sec), obtained with phase velocity inversions, are similar to that (=3.89 km/sec) found byHwang (1985) to the eastern South American region, while group velocity inversions have presented shear velocity (=3.75 km/sec) similar to that (=3.78 km/sec) found byLazcano (1972) to the Brazilian shield. It was not possible to define sharply the crust-mantle transition, but an analysis of the phase and group velocity inversions results has indicated that the total thickness of the crust should be between 30 and 39 km. The crustal and upper mantle model, obtained with phase velocity inversion, can be used as a preliminary model for the Brazilian coast.  相似文献   

Evaluation of ferrous and ferric Mössbauer fractions     

E. De Grave  A. Van Alboom 《Physics and Chemistry of Minerals》1991,18(5):337-342

The Mössbauer fractions f for various ferrous- and/or ferric-containing oxides and oxyhydroxides, silicates and carbonates were evaluated from the experimental temperature dependence of their center shifts, using the Debye approximation for the second-order Doppler shift. It is concluded that ferrous ions exhibit a lower fraction as compared to ferric ions. Using standard mixtures of -Fe₂O₃ with selected Fe²⁺ or Fe³⁺ compounds, it is found that the calculated Fe³⁺ f values are somewhat overestimated with respect to those of Fe²⁺. Possible explanations for this shortcoming are discussed and it is suggested that a different temperature dependence of the intrinsic isomer shift is the most likely reason. This suggestion is corroborated by analyses of hematite and hedenbergite data which are available for temperatures up to 900 K and 800 K respectively.  相似文献   

The geochemistry of gem opals as evidence of their origin     

Eloïse Gaillou  Aurlien Delaunay  Benjamin Rondeau  Martine Bouhnik-le-Coz  Emmanuel Fritsch  Guy Cornen  Christophe Monnier 《Ore Geology Reviews》2008,34(1-2):113

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   

Coupled redox transformations of catechol and cerium at the surface of a cerium(III) phosphate mineral     

Javiera Cervini-Silva  Benjamin Gilbert  Sirine Fakra  Stephan Friedlich  Jillian Banfield   《Geochimica et cosmochimica acta》2008,72(10):2454-2464

Highly insoluble Ce-bearing phosphate minerals form by weathering of apatite [Ca₅(PO₄)₃.(OH,F,Cl)], and are important phosphorous repositories in soils. Although these phases can be dissolved via biologically-mediated pathways, the dissolution mechanisms are poorly understood. In this paper we report spectroscopic evidence to support coupling of redox transformations of organic carbon and cerium during the reaction of rhabdophane (CePO₄·H₂O) and catechol, a ubiquitous biogenic compound, at pH 5. Results show that the oxic–anoxic conditions influence the mineral dissolution behavior. Under anoxic conditions, the release of P and Ce occurs stoichiometrically. In contrast, under oxic conditions, the mineral dissolution behavior is incongruent, with dissolving Ce³⁺ ions oxidizing to CeO₂. Reaction product analysis shows the formation of CO₂, polymeric C, and oxalate and malate. The presence of more complex forms of organic carbon was also confirmed. Near edge X-ray absorption fine structure spectroscopy measurements at Ce-M_4,5 and C-K absorption edges on reacted CePO₄·H₂O samples in the absence or presence of catechol and dissolved oxygen confirm that (1) the mineral surface converts to the oxide during this reaction, while full oxidation is limited to the near-surface region only; (2) the Ce valence remains unchanged when the reaction between CePO₄·H₂O and O₂ but in the absence of catechol. Carbon K-edge spectra acquired from rhabdophane reacted with catechol under oxic conditions show spectral features before and after reaction that are considerably different from catechol, indicating the formation of more complex organic molecules. Decreases in intensity of characteristic catechol peaks are accompanied by the appearance of new π^* resonances due to carbon in carboxyl (ca. 288.5 eV) and carbonyl (ca. 289.3 eV) groups, and the development of broad structure in the σ^* region characteristic of aliphatic carbon. Evolution of the C K-edge spectra is consistent with aromatic-ring cleavage and polymerization. These results further substantiate that the presence of catechol, O₂ (aq) causes both the oxidation of structural Ce³⁺ and the transformation of catechol to more complex organic molecules. Scanning Transmission X-Ray Microscopy measurements at the C K and Ce M_4,5 edges indicate three dominant organic species, varying in complexity and association with the inorganic phase. Untransformed catechol is loosely associated with CeO₂, whereas more complex organic molecules that exhibit lower aromaticity and stronger CO π^* resonances of carboxyl-C and carbonyl-C groups are only found in association with the grains. These results further serve as basis to postulate that, in the presence of O₂, CeO₂ can mediate the oxidative polymerization of catechol to form higher molecular weight polymers. The present work provides evidence for a pathway of biologically-induced, non-enzymatic oxidation of cerium and formation of small CeO₂ particles at room temperature. These findings may have implications for carbon cycling in natural and cerium-contaminated soils and aqueous environments.  相似文献   

Evidence for crustal degassing of CF₄ and SF₆ in Mojave Desert groundwaters     

Daniel A. Deeds  Martin K. Vollmer  Justin T. Kulongoski  Benjamin R. Miller 《Geochimica et cosmochimica acta》2008,72(4):999-1013

Dissolved tetrafluoromethane (CF₄) and sulfur hexafluoride (SF₆) concentrations were measured in groundwater samples from the Eastern Morongo Basin (EMB) and Mojave River Basin (MRB) located in the southern Mojave Desert, California. Both CF₄ and SF₆ are supersaturated with respect to equilibrium with the preindustrial atmosphere at the recharge temperatures and elevations of the Mojave Desert. These observations provide the first in situ evidence for a flux of CF₄ from the lithosphere. A gradual basin-wide enhancement in dissolved CF₄ and SF₆ concentrations with groundwater age is consistent with release of these gases during weathering of the surrounding granitic alluvium. Dissolved CF₄ and SF₆ concentrations in these groundwaters also contain a deeper crustal component associated with a lithospheric flux entering the EMB and MRB through the underlying basement. The crustal flux of CF₄, but not of SF₆, is enhanced in the vicinity of local active fault systems due to release of crustal fluids during episodic fracture events driven by local tectonic activity. When fluxes of CF₄ and SF₆ into Mojave Desert groundwaters are extrapolated to the global scale they are consistent, within large uncertainties, with the fluxes required to sustain the preindustrial atmospheric abundances of CF₄ and SF₆.  相似文献   

Benthic fluxes of mercury species in a lagoon environment (Grado Lagoon,Northern Adriatic Sea,Italy)     

Stefano Covelli  Jadran Faganeli  Cinzia De Vittor  Sergio Predonzani  Alessandro Acquavita  Milena Horvat 《Applied Geochemistry》2008

The role of the major biogeochemical processes in Hg cycling at the sediment–water interface was investigated in the Grado Lagoon (Northern Adriatic Sea). This wetland system has been extensively contaminated from the Idrija Hg Mine (Slovenia) through the Isonzo River suspended load carried by tidal fluxes. Three approaches were used to study the sediment–water exchange of total Hg (THg), methylmercury (MeHg), reactive Hg (RHg) and dissolved gaseous Hg (DGHg): (1) estimation of diffusive fluxes from porewater and overlying water concentrations, (2) measurements of benthic fluxes using a deployed light benthic chamber in situ and (3) measurements of benthic fluxes during oxic–anoxic transition with a laboratory incubation experiment. The THg solid phase, ranging between 9.5 and 14.4 μg g⁻¹, showed slight variability with depth and time. Conversely, MeHg contents were highest (up to 21.9 ng g⁻¹) at the surface; they tended to decrease to nearly zero concentration with depth, thus suggesting that MeHg production and accumulation occur predominantly just below the sediment–water interface. Porewater MeHg concentrations (0.9–7.9 ng L⁻¹, 0.15–15% of THg) varied seasonally; higher contents were observed in the warmer period. The MeHg diffusive fluxes (up to 17 ng m⁻² day⁻¹) were similar to those in the nearby Gulf of Trieste [Covelli, S., Horvat, M., Faganeli, J., Brambati, A., 1999. Porewater distribution and benthic flux of mercury and methylmercury in the Gulf of Trieste (Northern Adriatic Sea). Estuar. Coast. Shelf Sci. 48, 415–428], although the lagoon sediments contained four-fold higher THg concentrations. Conversely, the THg diffusive fluxes in the lagoon (up to 110 ng m⁻² day⁻¹) were one- to two-fold higher than those previously estimated for the Gulf of Trieste. The diurnal MeHg benthic fluxes were highest in summer at both sites (41,000 and 33,000 ng m⁻² day⁻¹ at the fishfarm and in the open lagoon, respectively), thus indicating the influence of temperature on microbial processes. The diurnal variations of dissolved THg and especially MeHg were positively correlated with O₂ and inversely with DIC, suggesting an important influence of benthic photosynthetic activities on lagoon benthic Hg cycling, possibly through the production of organic matter promptly available for methylation. The results from the dark chamber incubated in the laboratory showed that the regeneration of dissolved THg was slightly affected by the oxic–anoxic transition. Conversely, the benthic flux of MeHg was up to 15-fold higher in sediments overlain by O₂ depleted waters. In the anoxic phase, the MeHg fluxes proceeded in parallel with Fe fluxes and the methylated form reached approximately 100% of dissolved THg. The MeHg is mostly released into overlying water (mean recycling efficiency of 89%) until the occurrence of sulphide inhibition, due to scavenging of the available Hg substrate for methylation. The results suggest that sediments in the Grado Lagoon, especially during anoxic events, should be considered as a primary source of MeHg for the water column.  相似文献   

Editorial     

Z. Švestka  C. De Jager 《Solar physics》1969,8(1):3-4

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