Wolf-Rayet stars     

Allan J. Willis 《Astrophysics and Space Science》1996,237(1-2):145-168

This paper reviews the current status of knowledge regarding the basic physical and chemical properties of Wolf-Rayet stars; their overall mass loss and stellar wind characteristics and current ideas about their evolutionary status. WR stars are believed to be the evolved descendents of massive O-type stars, in which extensive mass loss reveals successive stages of nuclear processed material: WN stars the products of interior CNO-cycle hydrogen burning, and WC and WO stars the products of interior helium burning. Recent stellar evolution models, particularly those incorporating internal mixing, predict results which are in good accord with the different chemical compositions observationally inferred for WN, WC and WO stars. WR stars exhibit the highest levels of mass loss amongst earlytype stars: mass loss rates, typically, lie in the range [1–10]×10⁻⁵ M _⊙yr⁻¹. Radiation pressure-driven winds incorporating multi-scattering in high ionisation-stratified winds may cause these levels, but additional mechanisms may also be needed.  相似文献   

Some Characteristics of a Propagating Brittle Tensile Crack     

Merle E. Hanson  Allan R. Sanford 《Geophysical Journal International》1971,24(3):231-244

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Fall days of the SNC meteorites: Evidence for an SNC meteoroid stream,and a common site of origin     

Allan H. Treiman 《Meteoritics & planetary science》1992,27(1):93-95

Abstract— Four of the SNC meteorites of putative Martian origin are falls. Two of these fell on October 3: Chassigny in 1815 and Zagami in 1962. The probability of this coincidence arising from random fall days is approximately 1 in 60. If this coincidence is not the result of chance, it suggests that some of the SNC meteorites are derived from a meteoroid stream. In that Chassigny and Zagami span nearly the full range of SNC lithologies and histories, the coincidence of fall days is consistent with suggestions that all of the SNCs came from a single site (impact crater) on their parent planet.  相似文献   

The Balderton Sand and Gravel: Pre-Ipswichian cold stage fluvial deposits near Lincoln,England     

Allan Brandon  Michael G. Sumbler 《第四纪科学杂志》1991,6(2):117-138

The Balderton Terrace marks a former course of the River Trent between Newark and the Lincoln Gap. The principal deposit, the Balderton Sand and Gravel, is interpreted as a braided river sediment. Ice wedge casts truncated by intraformational erosion surfaces at many levels indicate syndepositional permafrost. Remnant cover deposits overlying the Balderton Sand and Gravel include the partly aeolian Whisby Sand. Locally, both the upper part of the Balderton Sand and Gravel and the cover deposits exhibit features indicative of temperate climate pedogenesis. All these deposits are affected by subsequent cryoturbation. On the basis of these features and the geomorphological and topographical relationship to other terrace deposits of the area, the Balderton Sand and Gravel and Whisby Sand are regarded as post-Hoxnian and pre-lpswichian, i.e. Wolstonian. Electron spin resonance age determinations for fossil elephant teeth and amino acid analyses on molluscs from the Balderton Sand and Gravel suggest correlation with Oxygen Isotope Stage 6. The Balderton Sand and Gravel has yielded a cold-climate mammalian fauna dominated by woolly mammoth and woolly rhinoceros, though rarer species suggest periods of milder climate. Silts from channels near the base of the deposit have produced pollen, mollusc, ostracod and beetle assemblages also indicating a cold climate.  相似文献   

The critical inclination problem: A simple treatment     

R. R. Allan 《Celestial Mechanics and Dynamical Astronomy》1970,2(1):121-122

A short analysis is presented in the hope of clarifying the situation.  相似文献   

Distribution of Uranium in the crust of the northwestern canadian shield as shown by lake-sediment analysis     

E.M. Cameron  R.J. Allan 《Journal of Geochemical Exploration》1973,2(3):237-250

In 1972 a reconnaissance geochemical survey was carried out by the Geological Survey of Canada in the northwestern Canadian Shield. Samples of nearshore lake sediment were collected, by helicopter, from 36,000 sq. miles of the Bear and Slave Structural Provinces. Sample density was one per 10 miles. These samples have since been analyzed for 27 elements. This paper is concerned with the distribution of uranium in 1,241 samples from the western third of the survey area. This region mainly comprises the Bear Province, of Proterozoic age.The Bear Province, which is a metallogenic province for uranium, also appears to be a geochemical province for this element. Uranium is four times more abundant in lake sediments from this area (5.3 p.p.m. U) as compared to the eastern part of the Slave Province (1.3 p.p.m. U). The lake-sediment data are in agreement with analyses of composite rock samples from two parts of the survey area.Within the Bear Province the regional distribution of uranium is controlled mainly by the distribution of Proterozoic granitic rocks. Nearly all areas of 5 p.p.m. U or greater in lake sediments are underlain by Proterozoic granites, or are near to these rocks. Within the granite areas, uranium is distributed along two sets of regularly spaced linear trends. The highest contents in lake sediment, which include values up to 300 p.p.m. U, commonly occur near the intersections of the two trends. These trends correspond to a set of northeast and a set of northwest strike-slip faults and lineaments that were produced by east-west compression of the Bear Province during and after the Hudsonian Orogeny (1750 m.y.). Outside the western margin of the survey area, complex epigenetic mineralization is associated with northeasterly-trending faults. Uranium has been produced from veins of this type at Port Radium and at the Rayrock Mine. Since it is associated with faults, this type of mineralization tends to occur in topographic depressions, that often contain lakes and swamps. Lake-sediment analysis is believed to be an excellent means of detecting such mineralization, both within the survey area and possibly elsewhere in the Canadian Shield. The data obtained during 1972 provide a basis for more detailed prospecting in the region.  相似文献   

Regime dependent changes in global precipitation   总被引：1，自引：1，他引：0  

Richard P. Allan 《Climate Dynamics》2012,39(3-4):827-840

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Molecular modelling of rare earth element complexation in subduction zone fluids     

Jelle van Sijl  Neil L. Allan  Wim van Westrenen 《Geochimica et cosmochimica acta》2009,73(13):3934-3947

Complexation of (trace) elements in fluids plays a critical role in determining element mobility in subduction zones, but to date, the atomic-scale processes controlling elemental solubilities are poorly understood. As a first step towards computer simulation of element complexation in subduction zone fluids, a thermodynamic cycle was developed to investigate the hydration environment and energetics of lanthanide complexes using density functional theory. The first solvation shell is explicitly defined and the remaining part of the aqueous fluid is modelled using a polarisable continuum model, which allows extrapolation to a broad pressure and temperature range.We illustrate our method by comparing solvation of lanthanide series elements in H₂O in the presence of fluoride or chloride for conditions relevant to subduction zones. The energetics of lanthanide- and lanthanide-fluoride/chloride hydration complexes were determined computationally. Calculated hydration free energies for trivalent lanthanides with explicit eight- and nine-fold coordinated first hydration shells show good agreement with literature data at room pressure and temperature. The hydration free energy is more negative for smaller complexes (heavy lanthanides) relative to larger complexes (light lanthanides), with the difference between La and Lu in water amounting to 361 kJ mol⁻¹. The hydration free energy of all lanthanide ions becomes less negative with increasing pressure (p) and temperature (T) up to 2.5 GPa and 1000 K (typical conditions in the upper part of subducting slabs). The free energy difference between light- and heavy-lanthanides remains essentially unchanged at elevated (p, T) conditions. There are minor geometrical differences in local hydration environment between light lanthanide-chloride (La-Nd) and heavy lanthanide-chloride (Pm-Lu) hydrated complexes, without a distinguishable energy difference. Complexation with fluoride is energetically more favourable than with chloride by 206 ± 4 kJ mol⁻¹ across the entire lanthanide series. The association of fluoride-water and chloride-water fragments with lanthanide-water complexes is energetically more favourable for aqueous lanthanide complexes surrounded by fewer first hydration shell water molecules.The methods developed in this study, in conjunction with simulation of the energetics of trace element incorporation into minerals, open the possibility to use molecular modelling to constrain elemental behaviour in subduction zones.  相似文献   

Electronic environments in carrollite, CuCo₂S₄, determined by soft X-ray photoelectron and absorption spectroscopy     

Alan N. Buckley  William M. Skinner  Allan Pring 《Geochimica et cosmochimica acta》2009,73(15):4452-4467

Fracture surfaces of a natural carrollite specimen have been characterised by synchrotron and conventional X-ray photoelectron spectroscopy and near-edge X-ray absorption spectroscopy. For the synchrotron X-ray measurements, the mineral surfaces were prepared under clean ultra high vacuum and were unoxidised. The characterisation was undertaken primarily to establish unequivocally the oxidation state of the Cu in the mineral, but also to obtain information on the electronic environments of the Co and S, and on the surface species. Experimental and simulated Cu L_2,3-edge absorption spectra confirmed an oxidation state of Cu^I, while Co 2p photoelectron and Co L_2,3 absorption spectra were largely consistent with the Co^III established previously by nuclear magnetic resonance spectroscopy. S 2p photoelectron spectra provided no evidence for S to be present in the bulk in more than one state, and were consistent with an oxidation state slightly less negative than S^-II. Therefore it was concluded that carrollite can be best represented by Cu^ICo^III₂(S₄)^-VII. The Cu^I oxidation state is in agreement with that expected for Cu tetrahedrally coordinated by S, but is in disagreement with the Cu^II deduced previously from some magnetic, magnetic resonance and Cu L-edge X-ray absorption spectroscopic measurements. A significant concentration of S species with core electron binding energies both lower and higher than the bulk value were formed at fracture surfaces, and these entities were assigned to monomeric and oligomeric surface S species. The density of Cu d states calculated for carrollite differed from that previously reported but was consistent with the observed Cu L₃ X-ray absorption spectrum. The initial oxidation of carrollite in air under ambient conditions was confirmed to be congruent, unlike the incongruent reaction undergone by a number of non-thiospinel sulfide minerals.  相似文献   

Towards molecular-level understanding of geochemical processes in mineral exploration     

Joël Brugger  Allan Pring  Frank Reith  Barbara Etschmann  Weihua Liu 《Journal of Geochemical Exploration》2009

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