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81.
In this paper, we examined the role of bedrock groundwater discharge and recharge on the water balance and runoff characteristics in forested headwater catchments. Using rigorous observations of catchment precipitation, discharge and streamwater chemistry, we quantified net bedrock flow rates and contributions to streamwater runoff and the water balance in three forested catchments (second‐order to third‐order catchments) underlain by uniform bedrock in Japan. We found that annual rainfall in 2010 was 3130 mm. In the same period, annual discharge in the three catchments varied from 1800 to 3900 mm/year. Annual net bedrock flow rates estimated by the chloride mass balance method at each catchment ranged from ?1600 to 700 mm/year. The net bedrock flow rates were substantially different in the second‐order and third‐order catchments. During baseflow, discharge from the three catchments was significantly different; conversely, peak flows during large storm events and direct runoff ratios were not significantly different. These results suggest that differences in baseflow discharge rates, which are affected by bedrock flow and intercatchment groundwater transfer, result in the differences in water balance among the catchments. This study also suggests that in these second‐order to third‐order catchments, the drainage area during baseflow varies because of differences between the bedrock drainage area and surface drainage area, but that the effective drainage area during storm flow approaches the surface drainage area. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
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B. Galle J. Mellqvist D.W. Arlander I. Fløisand M.P. Chipperfield A.M. Lee 《Journal of Atmospheric Chemistry》1999,32(1):147-164
Vertical columns of HF, HCl, HNO3, ClONO2, N2O, ClO and COF2 were measured at Harestua, Norway (60.22° N, 10.75° E, Elevation 600 a.s.l.) beginning on 24 November 1994 and concluding on 1 May 1995 during Phase-III of the SESAME (Second European Stratospheric Arctic and Mid-latitude Experiment) measurement campaign. The vertical columns of HCl, HNO3 and ClONO2 measured on 81 days were compared with columns calculated by the 3-D Cambridge model SLIMCAT. In addition the results were also interpreted by comparison with a photochemical trajectory model. Good agreement was seen for HCl while the nitrogen compounds showed larger discrepancies, especially for ClONO2. Evidence for chlorine activation was seen with 65% reduction of the chlorine reservoirs (HCl + ClONO2) while the levels of ClO were greatly enhanced. Interpretation of the loss with the trajectory model indicated condensation of chlorine on PSCs. The vertical column ratio of COF2 and HF was measured to 0.21 outside the vortex and a factor of two lower inside. The recovery of ClONO2 was seen to be much faster than that of HCl in the early spring. 相似文献
85.
利用精密量热仪测定了MgCl_2、MgCl_2·2H_2O、MgCl_2·4H_2O和MgCl_2·6H_2O在298.15°K溶于水的积分溶解热,并利用Pitzer电解质溶液的。~ΦL方程,计算了溶质的相对表观摩尔热焓,从而得到标准溶解焓分别为(KJ·mol~(-1))—155.86±0.17、—79.45±O.17,—41.78±O.18和—14.58±0.16;晶格能分别为—2490.36,—3158.37,—3772.70和—4376.56。二、四、六水合物的标准生成焓分别为—1289.39,—1898.72和—2497.58;水合焓分别为—76.41,—114.08和—141.28。 相似文献
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氯化钠存在下氯化亚锡-十六烷基三甲基氯化铵体系浮选分离复杂金属基体中锇 总被引:1,自引:0,他引:1
研究了氯化钠存在下氯化亚锡-十六烷基三甲基氯化铵体系对Os(Ⅳ)-三氯锡酸络阴离子的浮选行为。实验表明,在盐酸介质中,体系可以浮选分离Os(Ⅳ),其浮选率为95.2%。98.0%。方法加标回收率为94.0%-98.5%,精密度为2.1%-7.7%(RSD,n=5)。方法可用于从大量基体金属中分离Os(Ⅳ),对实际样品分离的分析结果与其他方法推荐值相符。 相似文献
89.
K. v. Czapiewski E. Czuba L. Huang D. Ernst A.L. Norman R. Koppmann J. Rudolph 《Journal of Atmospheric Chemistry》2002,43(1):45-60
The stable carbon isotope ratios of nonmethane hydrocarbons (NMHC) and methyl chloride emitted from biomass burning were determined by analyzing seven whole air samples collected during different phases of the burning process as part of a laboratory study of wood burning. The average of the stable carbon isotope ratios of emitted alkanes, alkenes and aromatic compounds is identical to that of the burnt fuel; more than 50% of the values are within a range of ±1.5 of thecomposition of the burnt fuel wood. Thus for the majority of NMHC emitted from biomass burning stable carbon isotope ratio of the burnt fuel a good first order approximation for the isotopic composition of the emissions. Of the more than twenty compounds we studied, only methyl chloride and ethyne differed in stable carbon isotope ratios by more than a few per mil from the composition of the fuel. Ethyne is enriched in 13C by approximately 20–30, and most of the variability can beexplained by a dependence on flame temperature. The 13C values decreaseby 0.019 /K (±0.0053/K) with increasing temperature. Methyl chloride is highly depleted in 13C, on average by25. However the results cover a wide range of nearly 30. Specifically, in two measurements with wood from Eucalyptus (Eucalyptus delegatensis) as fuel we observed the emission of extremely light methyl chloride (–68.5and–65.5). This coincides with higher than average emission ratiosfor methyl chloride (15.5 × 10–5 and 18 ×10–5 mol CH3Cl/mol CO2). These high emission ratios are consistent with the highchlorine content of the burnt fuel, although, due to the limited number of measurements, it would be premature to generalize these findings. The limited number of observations also prevents any conclusion on a systematic dependence between chlorine content of the fuel, emission ratios and stable carbon isotope ratio of methyl chloride emissions. However, our results show that a detailed understanding of the emissions of methyl chloride from chloride rich fuels is important for understanding its global budget. It is also evident that the usefulness of stable carbon isotope ratios to constrain the global budget of methyl chloride will be complicated by the very large variability of the stable carbon isotope ratio of biomass burning emissions. Nevertheless, ultimately the large fractionation may provide additional constraints for the contribution of biomass burning emissions to the atmospheric budget of methyl chloride. 相似文献
90.
Samira Krimissa Jean-Luc Michelot Lhoussaine Bouchaou Jacques Mudry Youssef Hsissou 《Comptes Rendus Geoscience》2004,336(15):1363-1369
The origin of chloride ions in groundwater from the Chtouka-Massa plain (Morocco) was studied by using chemical and isotopic analyses of water, and petrographic and chemical analyses of rocks. It appears that the schist formation, which forms the basement of the studied aquifer, is the main source of the high Cl? concentrations in groundwater. In these schists, chloride is, for a part, probably contained in biotites, and is released into groundwater through the weathering of these minerals. However, the exceptionally high chloride contents of these schists are difficult to explain if one does not assume that they also contain evaporitic-type minerals. To cite this article: S. Krimissa et al., C. R. Geoscience 336 (2004). 相似文献