The evolution of massive close binaries

The results of evolutionary computations for massive binary systems (initial masses of the primary 10M ) with mass ratios between 0.3 and 0.8 are summarized and compared with observations in order to verify how far one can go with the conservative assumption of mass exchange. It is found that conservative mass exchange leads to acceptable first-order models of W-R and massive X-ray binaries. However, the comparison between this theory and observation reveals that for the observed systems (W-R and X-ray binaries) a preference exists for low intial mass ratios; moreover, the X-ray luminosities of the theoretical models are systematically too low, though this may be due to the adopted wind model. In addition, the influences of several parameters (distance between the components, chemical composition, primary mass, mass ratio and atmosphere) are examined. These parameters influence the remnant mass and any further evolution only marginally. Attention is also given to the effect on the system parameters of a supernova explosion of the remnant of the mass-losing component. For a large range of systems a disruption probability smaller than 25% is found.     

210Pb balance in Long Island Sound

A material balance is constructed for excess ²¹⁰Pb (relative to ²²⁶Ra) as a test of the retentivity of Long Island Sound for a reactive heavy metal. Excess ²¹⁰Pb is supplied to Long Island Sound chiefly by direct atmospheric deposition [1 ± 0.2(dis·min^?1)cm^?2·yr^?1]. Rivers supply less than 20% of the atmospheric flux, and other inputs, from open ocean waters, ²²⁶Ra decay, groundwater seepage, and sewage discharge, appear to be negligible. The total input of excess ²¹⁰Pb represents approximately the flux required to maintain the inventory of excess ²¹⁰Pb measured in sediment cores from central Long Island Sound; that is, excess ²¹⁰Pb is lost from Long Island Sound chiefly by radioactive decay. The retention of excess ²¹⁰Pb within Long Island Sound is achieved in two steps: a rapid removal of soluble ²¹⁰Pb onto suspended particles and the ongoing entrapment of particles in the basin by the residual bottom-water influx from the east.     

Ferroan calcite replacement indicates former magnesian calcite skeletons

The replacement by ferroan calcite with preservation of the original structures can be used as a new criterion for identifying skeletons originally composed of high-magnesian calcite. This applies to bryozoa, rugose corals, echinoderms, many foraminifera, most ostracods, red algae, and serpulids. On the other hand, skeletons originally composed of low-magnesian calcite were never replaced by ferroan calcite, as shown by belemnites, brachiopods, and most of the pelecypods. Using this criterion, an original low-magnesian calcite composition is inferred for Tentaculites and some ostracods and foraminifera, whereas a previous high-magnesian calcite composition is inferred for trilobites, oligostegina and certain ooids. Chemical instability of high-magnesian calcite is suggested to be the driving force of the replacement by ferroan calcite. In most of the thirty-seven samples investigated, of Oligocene to Devonian age, the ferrous iron concentration of the interstitial fluid increased during diagenesis, as shown by well established sequences of cement A and B and fissure fill. This offers a relative time scale for diagenetic processes. Ferroan calcites contain up to 6 mol % FeCO₃ and up to 5 mol % MgCO₃. In this range of concentration, the distribution coefficients for Fe and Mg between calcite and solution at about 25°C are about 1 to 0-03, respectively, according to experiments. Possible sources of iron are iron oxides and hydroxides as well as clay minerals including glauconite. Though a submarine origin below the sediment surface is conceivable for ferroan calcite, there are serious limiting conditions such as low Eh and, at the same time, lack in sulphate-reducing bacteria. On the other hand, ferroan ‘dedolomite’, compositional zonality in individual ferroan calcite overgrowths, low δ¹⁸C and δ¹⁸O values, and low Mg concentrations point more to a meteoric-phreatic origin of many ferroan calcite occurrences.     

Calcretes of Olduvai Gorge and the Ndolanya Beds of northern Tanzania

Pedogenic calcretes are closely associated with Pliocene to Holocene wind-worked deposits of volcanic ash in the Olduvai and Ndolanya Beds of northern Tanzania. The typical profile with calcrete consists of an unconsolidated sediment layer, an underlying laminar calcrete, and a lowermost massive calcrete. The laminar calcrete is a relatively pure limestone, whereas massive calcrete is aeolian tuff cemented and replaced by calcite. An Olduvai calcrete profile can develop to a mature stage in only a few thousand years. Carbonatite ash was the dominant source for most of the calcite in the calcretes. Replacement was a major process in formation of the massive calcretes, and oolitic textures have resulted from micrite replacing pelletoid clay coatings around sand grains. Phillipsite and possible other zeolites were extensively replaced in the massive calcretes. Replacement of clay by micrite in the Olduvai calcretes is accompanied by dissolution or leaching of phengitic illite and the formation of clay approaching the composition of halloysite or kaolinite. In the upper calcrete of the Ndolanya Beds, montmorillonite was altered to a kaolinite-type mineral and to dioctahedral chlorite. Authigenic dolomite, zeolite, and dawsonite in the Olduvai calcretes probably received at least some of their components from replaced materials.     

Ice clathrate as a possible source of the atmospheres of the terrestrial planets

The presence and compositions of atmospheres on the terrestrial planets do not follow directly from condensation models which would have Earth accreting near 500°K. No single mechanism yet proposed adequately accounts for the abundances of noble gases and carbon and nitrogen in the atmospheres. We show that the composition of clathrates forming at low temperatures in cold regions of the nebula can be predicted. Addition of about 1 ppm clathrate material to the Earth can explain observed abundances of Ar, Kr, and Xe. Condensation and adsorption processes occuring at 400–500°K are necessary to explain the observed abundances of Ne, H₂O, C, and N. Possible sources of clathrates could be cometary bodies formed in the outer solar system.     

Analysis of stellar occultation data: Effects of photon noise and initial conditions

A new inversion technique for obtaining temperature, pressure, and number density profiles of a planetary atmosphere from an occultation light curve is described. This technique employs an improved boundary condition to begin the numerical inversion and permits the computation of errors in the profiles caused by photon noise in the light curve. We present our assumptions about the atmosphere, optics, and noise and develop the equations for temperature, pressure, and number density and their associated errors. By inverting in equal increments of altitude, Δh, rather than in equal increments of time, Δt, the inversion need not be halted at the first negative point on the light curve as required by previous methods. The importance of the boundary condition is stressed, and a new initial condition is given. Numerical results are presented for the special case of inversion of a noisy isothermal light curve. From these results, simple relations are developed which can be used to predict the noise quality of an occultation. It is found that fractional errors in temperature profiles are comparable to those of pressure and number density profiles. An example of the inversion method is shown. Finally, we discuss the validity of our assumptions. In an appendix we demonstrate that minimum fractional errors in scale height determined from the inversion are comparable to those from an isothermal fit to a noisy isothermal light curve.     

How to compare the surface of Io to laboratory samples

Since one does not know the photometric functions of various parts of Io, one cannot convert the observed geometric albedo of the satellite to a parameter more directly measurable in the laboratory. One must therefore convert laboratory reflectances to geometric albedos before quantitative comparisons between Io's surface and a laboratory sample are made. This procedure involves determining the wavelength dependence of the sample's photometric function. For substances such as sulfur, whose reflectance varies strongly with wavelength, it is incorrect to assume that the photometric function, and hence the ratio (laboratory reflectance/geometric albedo) is independent of wavelength. To illustrate this point, measurements of the color dependence of this ratio for sulfur are presented for the specific case in which the measured laboratory reflectance is the sample's normal reflectance. In general, unless the laboratory reflectance is precisely the geometric albedo, a wavelength-dependent correction factor must be determined before the laboratory sample can be compared quantitatively with Io's surface.