Indirect radiative forcing and climatic effect of the anthropogenic nitrate aerosol on regional climate of China   总被引：4，自引：0，他引：4  

李树  王体健  庄炳亮  韩永 《大气科学进展》2009,26(3):543-552

The regional climate model (RegCM3) and a tropospheric atmosphere chemistry model (TACM) were coupled, thus a regional climate chemistry modeling system (RegCCMS) was constructed, which was applied to investigate the spatial distribution of anthropogenic nitrate aerosols, indirect radiative forcing, as well as its climatic effect over China. TACM includes the thermodynamic equilibrium model ISORROPIA and a condensed gas-phase chemistry model. Investigations show that the concentration of nitrate aerosols is relatively high over North and East China with a maximum of 29 μg m^-3 in January and 8 μg m^-3 in July. Due to the influence of air temperature on thermodynamic equilibrium, wet scavenging of precipitation and the monsoon climate, there are obvious seasonal differences in nitrate concentrations. The average indirect radiative forcing at the tropopause due to nitrate aerosols is -1.63 W m^-2 in January and -2.65 W m^-2 in July, respectively. In some areas, indirect radiative forcing reaches $-$10 W m^-2. Sensitivity tests show that nitrate aerosols make the surface air temperature drop and the precipitation reduce on the national level. The mean changes in surface air temperature and precipitation are -0.13 K and -0.01 mm d^-1 in January and -0.09 K and -0.11 mm d^-1 in July, respectively, showing significant differences in different regions.  相似文献   

广州夏季雨水硝酸盐δ15N变化特征   总被引：3，自引：0，他引：3  

陈法锦  贾国东  陈建芳  张海生 《地球化学》2010,39(2):154-158

通过对广州2007年夏季雨水硝酸盐δ15的研究,讨论了广州地区雨水硝酸盐的主要来源及与之有关的大气化学演变过程。雨水硝酸盐占δ15N的变化趋势与N2O5含量的相似。暗示雨水硝酸盐δ15N与氮氧化合物的大气化学过程之间存在某种联系。白天雨水硝酸盐δ15N值偏低,与OH自由基氧化NOx生成硝酸盐的“白天反应”为主要反应相一致;18：00以后硝酸盐δ15N值呈升高趋势,则与N2O5累积的“夜间反应”成为主导反应相一致。因“白天反应”生成的HNO3的δ15N值受同位素分馏影响较小,白天雨水硝酸盐占δ15N值更能准确反映大气NOx的来源。白天雨水硝酸盐占δ15N平均值为2．5‰±2．1‰,表明除火力发电厂和机动车尾气排放来源外,雷电以及海源对大气NOx可能也有潜在贡献。  相似文献   

Tracing groundwater nitrate sources in the Dakar suburban area: an isotopic multi‐tracer approach     

M. Diédhiou  S. Cissé Faye  O. C. Diouf  S. Faye  A. Faye  V. Re  S. Wohnlich  F. Wisotzky  U. Schulte  P. Maloszewski 《水文研究》2012,26(5):760-770

The Dakar region is a mega city with multiple contaminant sources from urban expansion as well as industrial and agricultural activities. The major part of the region is underlain by unconfined sandy aquifer, which is vulnerable to contaminants derived from human land use. At present, the contaminated groundwater which extends over a large area in the suburban zone of Thiaroye poses a threat to the future of this valuable resource, and more specifically, a health threat. This study focuses on nitrate pollution occurrences and associated processes using nitrate isotope data (¹⁵N_NO3, ¹⁸O_NO3) combined with environmental isotopic tracers (¹⁸O, ²H, and ³H). Samples from 36 wells were collected to determine the level, distribution, and sources of contamination in relation to land use. Results indicate that shallow groundwater in the urbanized area of Thiaroye shows distinct evidence of surface contamination with nitrate as much as 300 mg/l NO₃^?. In rural area not serviced by water supply distribution network, much higher NO₃^? contents were found in few wells due to household and livestock feedlots. In most groundwater samples δ¹⁵N values ranged from + 10 to + 22‰, indicative of predominantly human and animal wastes. This was confirmed by environmental isotope data which suggest a mixture of polluted recharge waters. By using the dual δ¹⁵N vs δ¹⁸O as well as δ¹⁵N vs NO₃^? approach, denitrification may occur to some extent but it is blurred by mixing with new infiltrated nitrates and cycling derived from continuous leaky septic system. Results suggest that nitrate contamination of the aquifer is a consequence of unregulated urbanisation (homemade latrines), continuing contaminant transfer in shallow water depth where aerobic conditions prevail. Copyright © 2011 John Wiley & Sons, Ltd.  相似文献   

Hydrogeochemistry and environmental isotopes of ground water in Jeju volcanic island,Korea: implications for nitrate contamination     

Dong‐Chan Koh  Ho‐Wan Chang  Kwang‐Sik Lee  Kyung‐Seok Ko  Yongje Kim  Won‐Bae Park 《水文研究》2005,19(11):2225-2245

Ground water from springs and public supply wells was investigated for hydrochemistry and environmental isotopes of ³H, ¹⁸O and D in Jeju volcanic island, Korea. The wells are completed in a basaltic aquifer and the upper part of hydrovolcanic sedimentary formation. Nitrate contamination is conspicuous in the coastal area where most of the samples have nitrate concentrations well above 1 mg NO₃ N/l. Agricultural land use seems to have a strong influence on the distribution of nitrate in ground water. Comparison of stable isotopic compositions of precipitation and ground water show that ground water mostly originates from rainy season precipitation without significant secondary modification and that local recharge is dominant. ³H concentration of ground water ranged from nearly zero to 5 TU and is poorly correlated with vertical location of well screens. The occurrence of the ³H‐free, old ground water is due to the presence of low permeability layers near the boundary of the basaltic aquifer and the hydrovolcanic sedimentary formation, which significantly limits ground water flow from the upper basaltic aquifer. The old ground water exhibited background‐level nitrate concentrations despite high nitrate loadings, whereas young ground water had considerably higher nitrate concentrations. This correlation of ³H and nitrate concentration may be ascribed to the history of fertilizer use that has increased dramatically since the early 1960s in the island. This suggests that ³H can be used as a qualitative indicator for aquifer vulnerability to nitrate contamination. Copyright © 2005 John Wiley & Sons, Ltd.  相似文献   

The effect of transient storage on nitrate uptake lengths in streams: an inter‐site comparison     

Laura K. Lautz  Donald I. Siegel 《水文研究》2007,21(26):3533-3548

Surface water–groundwater interaction in the hyporheic zone may enhance biogeochemical cycling in streams, and it has been hypothesized that streams exchanging more water with the hyporheic zone should have more rapid nitrate utilization. We used simultaneous conservative solute and nitrate addition tracer tests to measure transient storage (which includes hyporheic exchange and in‐stream storage) and the rate of nitrate uptake along three reaches within the Red Canyon Creek watershed, Wyoming. We calibrated a one‐dimensional transport model, incorporating transient storage (OTIS‐P), to the conservative solute breakthrough curves and used the results to determine the degree of transient storage in each reach. The nitrate uptake length was quantified from the exponential decrease in nitrate concentration with distance during the tracer tests. Nitrate uptake along the most downstream reach of Red Canyon Creek was rapid (turnover time K^?1_c = 32 min), compared with nitrate uptake reported in other studies (K^?1_c = 12 to 551 min), but other sites within the watershed showed little nitrate retention or loss. The uptake length S_w‐NO^?₃ for the most downstream reach was 500 m and the mass transfer coefficient V_f‐NO^?₃ was 6·3 m min^?1. Results from 15 other nitrate‐addition tracer tests were used to create a regression model relating transient storage and measures of stream flow to nitrate uptake length. The model, which includes specific discharge and transient storage area, explains almost half the variability in nitrate uptake length (adjusted R² = 0·44) and is most effective for comparing sites with very different stream characteristics. Although large differences in specific discharge and storage zone area explain inter‐site differences in nitrate uptake, other unmeasured variables, such as available organic carbon and microbial community composition, are likely important for predicting differences in nitrate uptake between sites with similar specific discharge rates and storage zone areas, such as when making intra‐site comparisons. Copyright © 2007 John Wiley & Sons, Ltd.  相似文献   

Ground Based FTIR Measurements of Stratospheric Species from Harestua, Norway During Sesame and Comparison with Models     

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   

INTERACTIONS BETWEEN AMMONIUM UPTAKE AND NITRATE UPTAKE BY NATURAL PHYTOPLANKTONASSEMBLAGES   总被引：4，自引：0，他引：4  

焦念志 《中国海洋湖沼学报》1993,11(2):97-107

Measurements of ammonium and nitrate uptakes by natural phytoplankton assemblages from Jiaozhou Bay at various combinations of ammonium and nitrate concentrations with 15N trace techniques showed that uptake rate of either nitrogen was influenced by the presence of the other but that the influence of ammonium on nitrate uptake was much greater than, that of nitrate on ammonium uptake. The influence mechanism of ammonium on nitrate uptake manifested as competition at lower concentrations and as inhibition at higher concentrations (ammonium concentration >0.6 umol/L), but no total inhibition appeared within the concentration.range of the experiments (0-10umol/L). The influence of nitrate on ammonium uptake seems to be a result of competition for uptake sites on the cell surface. In view of the in situ nutrient concentration in the given marine . environment, it is believed that both nitrogen sources are utilized by phytoplankton. Nitrate uptake in the presence of ammonium and ammonium uptake in the presen  相似文献   

硝酸根对颗粒状铁降解三氯乙烯的影响(英文)     

Qiong LU　 Lai GUI　 Robert W.GILLHAM 《地学前缘》2005,12(Z1):176-183

为研究硝酸根对颗粒状铁降解三氯乙烯的影响,进行了柱实验和相应的反应铁腐蚀电位测定。在硝酸根离子存在条件下,铁的腐蚀电位相应升高,系统条件也因之发生变化,导致钝性的铁氧化物在铁表面生成。因而,三氯乙烯和硝酸根离子降解速率明显减小, 并且降解速率减小的程度与硝酸根离子的浓度成比例。当污染液流过反应柱时,硝酸根离子与铁反应, 被还原为氨根离子。该反应造成硝酸根离子的浓度梯度,使钝化区在柱中上移,从而影响了三氯乙烯的降解曲线。与三氯乙烯单独与铁反应相比,当含4 7 mg/L硝酸根的三氯乙烯溶液流经反应柱170 孔隙体积后,降解50% 三氯乙烯所需的时间(t50) 从小于4 h增加到大于10 h;而当三氯乙烯溶液中加入100 mg/L硝酸根离子,仅17 孔隙体积溶液流经反应柱后,三氯乙烯降解t50就已大于14 h。研究结果表明,由于硝酸根离子对铁的腐蚀电位和铁表面氧化膜的不利作用,在处理靶污染物为高浓度硝酸根离子和三氯乙烯共同污染的地下水时,铁渗透反应隔栅不是最佳选择。如果靶污染物中硝酸根离子浓度比较低,则在设计铁隔栅时应考虑到硝酸根离子造成的不利因素,相应增加铁墙的厚度,从而确保三氯乙烯的降解效果。  相似文献   

Using the dual isotopes approach to identify the nitrate sources of karst groundwater, Guiyang, Southwest China     

《中国地球化学学报》2006,25(B08):173-174

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Gaseous and Particulate Oxidized and Reduced Nitrogen Species in the Atmospheric Boundary Layer in Scandinavia in Spring     

Asgeir Sorteberg  Øystein Hov  Sverre Solberg  Kjetil Tørseth  Hans Areskoug  Martin Ferm  Kit Granby  Heikki Lättilä  Karin Persson  David Simpson 《Journal of Atmospheric Chemistry》1998,30(2):241-271

Observations of the concentration of several nitrogen containing compounds at five rural Scandinavian sites during March–June 1993 are reported. Total nitrate (NO ₃ ^- + HNO₃) and total ammonium (NH ₄ ⁺ + NH₃) were measured by denuder and filter pack. In general the methods agree well. At all sites the particulate fraction dominated, with the largest fraction of NO ₃ ^- and the lowest of NH ₄ ⁺ at the sites which were closest to the emission sources. The fraction of NO ₃ ^- of total nitrate increased with increasing NO₂ concentrations, indicating that the nighttime conversion of NO₂ to NO ₃ ^- is an important route of formation for NO ₃ ^- . A positive correlation was found between HNO₃ and O₃ in June at all sites, while no correlation was found early in the spring. Model calculations were made with a lagrangian boundary layer photooxidant model for the whole period, and compared to the measured concentrations. The calculated ratio between mean observed and modelled daily maximum concentrations of ozone over the measurement period were within +/–10% at all sites. The models ability to describe the daily ozone maximum concentration was satisfactory with an average deviation of 19–22% from the observed concentrations. HNO₃ was underestimated by over 50% at all sites except the one closest to the emission sources. The correlation between modelled and observed concentrations was generally best for the sites with shortest transport distance from the sources of emission.  相似文献