Studies have been made of the boron content and distribution in recent Mytilus edulis shells by mapping the alpha particle distribution produced by the 10B (n,α)7Li reaction using cellulose nitrate track detectors. Boron is concentrated in the inorganic parts of the shell matrix and is enriched in aragonite relative to calcite by a factor of 1.5–2. The B contents in different parts of individual shells and in different specimens from a given locality are well defined, particularly for the aragonite layer. A correlation was found between the B in the aragonite layer and the salinity of the water in which the shells grew. The method shows promise as a means of using the boron content of fossil shells to determine paleosalinity. 相似文献
Growth rates of four Pacific ferromanganese deposits have been determined by uranium-series and hydration-rind dating techniques. This represents the first time these two methods have been applied to the same samples. Of the four samples analyzed, two agree in both techniques and two show a wide disparity. The samples that do not agree have uranium-series rates which are low compared to those deduced by the hydration-rind techniques. The same samples also display steep232Th activity gradients in the outer layers of the ferromanganese material. Since the half-life of232Th is extremely long (1010 yr), these gradients could not be due to radioactive decay. This suggests that the distribution of230Th, at least in these cases, may also be a result of some process other than radioactive decay.One of our samples which has a steep232Th gradient produces a230Th “exposure age” which is indistinguishable to the calculated hydration age within the analytical uncertainty. The rate of growth calculated on the basis of the slope of the decline of230Th within the deposit, however, is low by over one order of magnitude when compared to the rate determined by the hydration-rind method. Although previous results indicate that the distribution of232Th is usually quite random within ferromanganese deposits, our results indicate that caution should be exercised when assessing their growth rates on the basis of uranium-series results. 相似文献
Examination of odd-hydrogen production and loss processes in the lower stratosphere reveals that the large abundances of midlatitude ClO recently measured requires a reassessment of the OH yield from methane oxidation due to a more rapid initiation of the methane oxidation sequence by atomic chlorine. Using a steady state calculation for OH and an iterative procedure for evaluating odd-hydrogen production from the methane oxidation sequence, we demonstrate that both OH and reactive chlorine are amplified below 25 km. The amplified values of OH and ClO are found to be consistent with recent measurements of ClO concentrations and of OH column abundances. 相似文献
The diffusion of Xe in olivine, a major mineral in both meteorites and lunar samples, was studied. Xe ions were implanted at 200 keV into single-crystal synthetic-forsterite targets and the depth profiles were measured by alpha particle backscattering before and after annealing for 1 hour at temperatures up to 1500°C. The fraction of implanted Xe retained following annealing was strongly dependent on the implantation dose. Maximum retention of 100% occurred for an implantion dose of 3 × 1015 Xe ions/cm2. Retention was less at lower doses, with ≥ 50% loss at 1 × 1014 Xe ions/cm2. Taking the diffusion coefficient at this dose as a lower limit, the minimum activation energy necessary for Xe retention in a 10 μm layer for 107 years was calculated as a function of metamorphic temperature. For example, an activation energy of 50 kcal/mole implies Xe retention may be possible for metamorphic temperatures below 500°C. 相似文献
Pore water chemistry (total dissolved CO2, NH4, NO3, NO2, PO4, Si(OH)4, Ca, Mg, Fe, Mn, SO4, H2S and F, and titration alkalinity), solid phase chemistry (Corg, Porg, CTOT, NTOT, F, SiOPAL and SII), and sediment characteristics (porosity, dry bulk density and formation factors) were determined on a centimeter-scale spacing in the upper 20–40 cm of sediments under intense upwelling areas on the Peru continental shelf. These data demonstrate that carbonate fluorapatite (CFA) is precipitating from pore waters in the upper few centimeters of a gelatinous mud with high organic carbon content (up to 20% Corg), very high porosity ( > 0.96 ml cm−3) and very low dry bulk density (< 0.1 g cm−3). Dissolved phosphate concentrations at the sediment-water interface range from 20 to 100 μM, orders of magnitude higher than bottom-water concentrations, and much higher than predicted from regeneration of organic matter. The mechanism of this interfacial phosphate release is unclear, but is apparently uncoupled from carbon and nitrogen metabolism and thus may be linked either to dissolution of fish debris or to the presence of a microbial mat in surficial sediments. Fluoride is incorporated into CFA by diffusion from the overlying seawater, and carbonate ions are provided from pore-water alkalinity. Magnesium concentrations in this reaction zone are not significantly different from those of seawater, suggesting that magnesium depletion is not a necessary prerequisite for CFA precipitation.
The environment of precipitation is interface-linked rather than driven by organic diagenesis of phosphorus deeper in the sediment. Most of the cores display a wide range of diagenetic characteristics below the immediate interfacial region, but almost all show the precipitation signature near the interface. This interface-linked early diagenetic porewater environment for the precipitation of CFA explains many of the geochemical characteristics of phosphorites and provides a “testable” model to compare the modern phosphogenic analog with ancient phosphorite deposits. Two of the cores display very high solid phase phosphorus and fluoride contents reflecting the presence of apparently modern pelletal apatites. 相似文献
Electron probe microanalyser measurements of trace elements with high accuracy are challenging. Accurate Al measurements in olivine are required to calibrate SIMS implant reference materials for measurement of Al in the solar wind. We adopt a combined EPMA/SIMS approach that is useful for producing SIMS reference materials as well as for EPMA at the ~ 100 µg g?1 level. Even for mounts not polished with alumina photoelectron spectroscopy shows high levels of Al surface contamination. In order to minimise electron beam current density, a rastered 50 × 100 µm electron beam was adequate and minimised sensitivity to small Al‐rich contaminants. Reproducible analyses of eleven SIMS‐cleaned spots on San Carlos olivine agreed at 69.3 ± 1.0 µg g?1. The known Al mass fraction was used to calibrate an Al implant into San Carlos. Accurate measurements of Al were made for olivines in the pallasites: Imilac, Eagle Station and Springwater. Our focus was on Al in olivine, but our technique could be refined to give accurate electron probe measurements for other contamination‐sensitive trace elements. For solar wind, it is projected that the Al/Mg abundance ratio can be determined to 6%, a factor of 2 more precise than the solar spectroscopic ratio. 相似文献