Hot stars in old stellar populations: a continuing need for intermediate ages

We present numerical investigations into the formation of massive stars from turbulent cores of density structure  ρ∝ r ^−1.5  . The results of five hydrodynamical simulations are described, following the collapse of the core, fragmentation and the formation of small clusters of protostars. We generate two different initial turbulent velocity fields corresponding to power-law spectra   P ∝ k ⁻⁴  and   P ∝ k ^−3.5  , and we apply two different initial core radii. Calculations are included for both completely isothermal collapse, and a non-isothermal equation of state above a critical density  (10⁻¹⁴ g cm⁻³)  . Our calculations reveal the preference of fragmentation over monolithic star formation in turbulent cores. Fragmentation was prevalent in all the isothermal cases. Although disc fragmentation was largely suppressed in the non-isothermal runs due to the small dynamic range between the initial density and the critical density, our results show that some fragmentation still persisted. This is inconsistent with previous suggestions that turbulent cores result in the formation of a single massive star. We conclude that turbulence cannot be measured as an isotropic pressure term.     

Systematics of calcium partitioning between olivine and silicate melt: implications for melt structure and calcium content of magmatic olivines

A systematic characterization of the chemical factors that control calcium partitioning between olivine and melt in a magmatic environment was undertaken using experiments performed on compositionally simple systems (CaO-MgO-SiO₂, CaO-MgO-Al₂O₃-SiO₂, CaO-MgO-Al₂O₃-SiO₂-Cr₂O₃, CaO-MgO-Al₂O₃-SiO₂-TiO₂, CaO-MgO-Al₂O₃-SiO₂-Na₂O, CaO-MgO-Al₂O₃-SiO₂-FeO, CaO-MgO-Al₂O₃-SiO₂-FeO-Na₂O) over a wide range of temperature (1050–1530 °C) at one bar pressure. The calcium concentration of olivines is shown to be dependent not only on the forsterite content of the olivine but to a large extent on melt composition. For a fixed CaO content of the melt, these results show that the CaO concentration of olivine is strongly sensitive to the amount of alumina, alkali and ferrous iron present in the coexisting melt. Oxygen fugacity and temperature are not found directly to affect Ca partitioning. It is thus proposed that the systematic variations of the calcium content of olivine may be used as an “in-situ chemical potentiometer” of the lime activity of the melt. Based upon these data in synthetic systems, an empirical model describing Ca partitioning between olivine and melt is developed. When applied to natural olivines this model reproduces their Ca content, where melt composition is known, to within ±10% relative. The model may therefore be used to predict changes in melt composition during olivine crystallization and/or to assess whether an olivine is in equilibrium with its host magma. Finally, the wide range of Ca partitioning observed at fixed crystal composition confirms that minor element partitioning between crystal and melt cannot be predicted from the physical characteristics of the crystal alone, and that the non-ideality of the melt has to be taken into account. Received: 12 June 1998 / Accepted: 1 February 1999     

Climate and climate change in western canada as simulated by the Canadian regional climate model

Abstract

A þrst climate simulation performed with the novel Canadian Regional Climate Model (CRCM) is presented. The CRCM is based on fully elastic non‐hydrostatic þeld equations, which are solved with an efþcient semi‐implicit semi‐Lagrangian (SISL) marching algorithm, and on the parametrization package of subgrid‐scale physical effects of the second‐generation Canadian Global Climate Model (GCMII). Two 5‐year integrations of the CRCM nested with GCMII simulated data as lateral boundary conditions are made for conditions corresponding to current and doubled CO₂ scenarios. For these simulations the CRCM used a grid size of 45 km on a polar‐stereographic projection, 20 scaled‐height levels and a time step of 15 min; the nesting GCMII has a spectral truncation of T32, 10 hybrid‐pressure levels and a time step of 20 min. These simulations serve to document: (1) the suitability of the SISL numerical scheme for regional climate modelling, (2) the use of GCMII physics at much higher resolution than in the nesting model, (3) the ability of the CRCM to add realistic regional‐scale climate information to global model simulations, and (4) the climate of the CRCM compared to that of GCMII under two greenhouse gases (GHG) scenarios.     

The geochemistry of gem opals as evidence of their origin

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.     

The UBV orbital phase curves of Rhea,Dione, and Tethys

Orbital phase curves are reported for Rhea (SV), Dione (SIV), and Tethys (SIII). Variations of 0.2 mag. and 0.8 mag. were found for Rhea and Dione respectively, while no variation of Tethys was detected. Some color variations are also reported.     

Effects of scattered solar radiation and absorption by SO2 on the photodissociation processes in the stratosphere of Venus

In the stratosphere of Venus, the available luminous flux which locally produces the photodissociation processes at a given altitude may be divided into three parts: direct incoming downward flux, flux resulting from the reflection on the surface of the clouds, and flux due to molecular scattering. A relatively simple computation method has been used to evaluate the relative importance of these three parts at altitudes between 65 and 100 km. It is shown that the extra contribution of the reflected and scattered fluxes to photodissociation processes cannot be neglected in the uv and visible regions. In the case of SO₂, for instance, which presents an absorption band in the uv, the photodissociation coefficient is increased 30% due to these effects. Calculations of the photodissociation coefficients of CO₂, O₃, H₂S, and SO₂ are presented. As a result of the increase by 60% in the ozone photolysis rate, the calculated O₂ infrared band at 1.27 μm is larger by a factor of nearly 2 than is expected from a calculation without taking albedo or scattering into account.     

Factors affecting rural landholders’ adaptation to climate change: Insights from formal institutions and communities of practice

This study explores the factors affecting rural landholders’ adaptation to climate change from the perspectives of formal institutions and communities of practice. Semi-structured interviews were conducted with formal institutions (e.g. South Australian government agencies) and communities of practice (e.g. farm systems groups) within two natural resource management regions in South Australia. Both groups noted that rural landholders autonomously adapt to a variety of risks, including those induced by climate variability; however, the types and levels of adaptation varied among individuals as a result of variety of barriers to adaptation. The lack of communication and engagement processes established between formal institutions and communities of practice was one major barrier. The paper presents and discusses a model for transferring knowledge and information on climate change among formal institutions, communities of practice, trusted individual advisors and rural landholders, and for supporting the co-management of climate change across multiple groups in rural agricultural areas in Australia and elsewhere.