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Recently, a new method has been introduced for the estimation of photosynthetic oxygen production from the triple isotope composition (δ17O and δ18O) of dissolved O2 in the ocean and of air O2 in ice cores. This method is based on the deviations (17Δ) from mass dependent respiratory fractionation, the major process affecting the isotopic composition of air O2. To apply this method, the slope in the 17O/16O vs. 18O/16O relationship used for 17Δ calculation must be known with high accuracy. Using numerical simulations and closed system experiments, we show how the respiratory slope is manifested in the 17Δ of O2 in situations where respiration is the only process affecting oxygen isotopic composition (kinetic slope), and in systems in steady state between photosynthesis and respiration (steady state slope). The slopes of the fractionation line in these two cases are different, and the reasons of this phenomenon are discussed. To determine the kinetic respiratory slope for the dominant O2 consumers in aquatic systems, we have conducted new experiments using a wide range of organisms and conditions and obtained one universal value (0.5179 ± 0.0006) in ln(δ17O + 1) vs. ln(δ18O + 1) plots. It was also shown that the respiratory fractionations under light and dark are identical within experimental error. We discuss various marine situations and conclude that the kinetic slope 0.518 should be used for calculating 17Δ of dissolved O2. In contrast, a steady state fractionation slope should be used in global mass balance calculations of triple isotope ratios of O2 in air records of ice cores. 相似文献
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The variations of δ17O and δ18O in recent meteoric waters and in ice cores have proven to be an important tool for investigating the present and past hydrologic cycle. In order to close significant information gaps in the present distribution of δ17O and δ18O of meteoric water, we have run precise measurements, with respect to VSMOW, on samples distributed globally from low to high latitudes. Based on the new and existing data, we present the Global Meteoric Water Line (GMWL) for δ17O and δ18O as:
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Vertical profiles of temperature and humidity were measured over the sea in two series of 48 hours each, during the summer near the Israeli coast of the Mediterranean. A prominent inversion was observed in the temperature profiles. In the first series the average height of the inversion base was 350m and in the second, 600m. In the inversion a very sharp decrease of the absolute humidity was found. Below the inversion down to the sea surface the atmosphere was well mixed. A significant diurnal oscillation was observed at the height of the inversion base. During the day the inversion moved up and during the night it moved down. This movement was 250m in the first series and 450m in the second. The movement of the inversion base was almost adiabatic. It is suggested that the fluctuation in the height of the inversion base is mainly due to the developing breeze. 相似文献
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The isotopic composition of atmospheric O2 depends on the rates of oxygen cycling in photosynthesis, respiration, photochemical reactions in the stratosphere and on δ17O and δ18O of ocean and leaf water. While most of the factors affecting δ17O and δ18O of air O2 have been studied extensively in recent years, δ17O of leaf water—the substrate for all terrestrial photosynthesis—remained unknown. In order to understand the isotopic composition of atmospheric O2 at present and in fossil air in ice cores, we studied leaf water in field experiments in Israel and in a European survey. We measured the difference in δ17O and δ18O between stem and leaf water, which is the result of isotope enrichment during transpiration. We calculated the slopes of the lines linking the isotopic compositions of stem and leaf water. The obtained slopes in ln(δ17O + 1) vs. ln(δ18O + 1) plots are characterized by very high precision (∼0.001) despite of relatively large differences between duplicates in both δ17O and δ18O (0.02-0.05‰). This is so because the errors in δ18O and δ17O are mass-dependent. The slope of the leaf transpiration process varied between 0.5111 ± 0.0013 and 0.5204 ± 0.0005, which is considerably smaller than the slope linking liquid water and vapor at equilibrium (0.529). We further found that the slope of the transpiration process decreases with atmospheric relative humidity (h) as 0.522-0.008 × h, for h in the range 0.3-1. This slope is neither influenced by the plant species, nor by the environmental conditions where plants grow nor does it show strong variations along long leaves. 相似文献
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Variations in oxygen and hydrogen isotope ratios of water and ice are powerful tools in hydrology and ice core studies. These variations are controlled by both equilibrium and kinetic isotope effects during evaporation and precipitation, and for quantitative interpretation it is necessary to understand how these processes affect the isotopic composition of water and ice. Whereas the equilibrium isotope effects are reasonably well understood, there is controversy on the magnitude of the kinetic isotope effects of both oxygen and hydrogen and the ratio between them. In order to resolve this disagreement, we performed evaporation experiments into air, argon and helium over the temperature range from 10 to 70 °C. From these measurements we derived the isotope effects for vapor diffusion in gas phase (εdiff(HD16O) for D/H and εdiff(H218O) for 18O/16O). For air, the ratio εdiff(HD16O)/εdiff(H218O) at 20 °C is 0.84, in very good agreement with Merlivat (1978) (0.88), but in considerable inconsistency with Cappa et al. (2003) (0.52). Our results support Merlivat’s conclusion that measured εdiff(HD16O)/εdiff(H218O) ratios are significantly different than ratios calculated from simplified kinetic theory of gas diffusion. On the other hand, our experiments with helium and argon suggest that this discrepancy is not due to isotope effects of molecular collision diameters. We also found, for the first time, that the εdiff(HD16O)/εdiff(H218O) ratio tends to increase with cooling. This new finding may have important implications to interpretations of deuterium excess (d-excess = δD − 8δ18O) in ice core records, because as we show, the effect of temperature on d-excess is of similar magnitude to glacial interglacial variations in the cores. 相似文献
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We developed a new semi-analytical source zone depletion model (SZDM) for multicomponent light nonaqueous phase liquids (LNAPLs) and incorporated this into an existing screening model for estimating cleanup times for chemical spills from railroad tank cars that previously considered only single-component LNAPLs. Results from the SZDM compare favorably to those from a three-dimensional numerical model, and from another semi-analytical model that does not consider source zone depletion. The model was used to evaluate groundwater contamination and cleanup times for four complex mixtures of concern in the railroad industry. Among the petroleum hydrocarbon mixtures considered, the cleanup time of diesel fuel was much longer than E95, gasoline, and crude oil. This is mainly due to the high fraction of low solubility components in diesel fuel. The results demonstrate that the updated screening model with the newly developed SZDM is computationally efficient, and provides valuable comparisons of cleanup times that can be used in assessing the health and financial risk associated with chemical mixture spills from railroad-tank-car accidents. 相似文献
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