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1.
Carbon sequestration in soil organic matter of degraded Sahelian agro-ecosystems could play a significant role in the global carbon (C) uptake through terrestrial sinks while, simultaneously, contributing to sustainable agriculture and desertification control. The paper documents the results of a two-year pilot project in Senegal assessing real project opportunities with main emphasis on the West-Central Agricultural Region (Old Peanut Basin). Current total system C content in this region, calculated on the basis of in situ soil and biomass carbon measurements, amounted to 28 t ha–1 with 11 t C ha–1 in soils (0–20 cm) and 6.3 t C ha–1 in trees. Potential changes in soil C, simulated with CENTURY for a 25-year period, ranged from –0.13 t C ha–1 yr–1 under poor management to +0.43 t C ha–1 yr–1 under optimum agricultural intensification. Simulated changes in crop yields varied from –62% to +200% under worst and best management scenarios respectively. Best management practices that generate the highest sequestration rates are economically not feasible for the majority of local smallholders, unless considerable financial support is provided. Especially when applied on a larger scale, such packages risk to undermine local, opportunistic management regimes and, in the long run, also the beneficiaries capacity to successfully adapt to their constantly changing environment.  相似文献   

2.
Carbon sequestration in soil organic matter of degraded Sahelian agro-ecosystems could play a significant role in the global carbon (C) uptake through terrestrial sinks while, simultaneously, contributing to sustainable agriculture and desertification control. The paper documents the results of a two-year pilot project in Senegal assessing real project opportunities with main emphasis on the West-Central Agricultural Region (Old Peanut Basin). Current total system C content in this region, calculated on the basis of in situ soil and biomass carbon measurements, amounted to 28 t ha–1 with 11 t C ha–1 in soils (0–20 cm) and 6.3 t C ha–1 in trees. Potential changes in soil C, simulated with CENTURY for a 25-year period, ranged from –0.13 t C ha–1 yr–1 under poor management to +0.43 t C ha–1 yr–1 under optimum agricultural intensification. Simulated changes in crop yields varied from –62% to +200% under worst and best management scenarios respectively. Best management practices that generate the highest sequestration rates are economically not feasible for the majority of local smallholders, unless considerable financial support is provided. Especially when applied on a larger scale, such packages risk to undermine local, opportunistic management regimes and, in the long run, also the beneficiaries capacity to successfully adapt to their constantly changing environment.  相似文献   

3.
In the present study, the wet and dry depositions of particulate NO3−, SO42−, Cl− and NH4+ were measured using a wet/dry sampler as a surrogate surface. Gas phase compounds of nitrogen, sulfur and chloride (HNO3, NH3, SO2 and HCl) were measured by an annular denuder system (ADS) equipped with a back up filter for the collection of particles with diameter ≤ 5 μm. Ambient concentrations of NO, NO2 and SO2 were also taken into consideration. Sampling was conducted at an urban site in the center of the city of Thessaloniki, northern Greece. The presence of the aerosol species was examined by cold/warm period and the possible compounds in dry deposits were also considered. Dry deposition fluxes were found to be well correlated with ambient particle concentrations in order to be used for the calculation of particle deposition velocity. Average particulate deposition velocities calculated were 0.36, 0.20, 0.20 and 0.10 cm s− 1 for Cl−, NO3−, SO42− and NH4+, respectively. Total dry deposition fluxes (gas and particles) were estimated at 3.24 kg ha− 1 year− 1 for chloride (HCl + p-Cl), 9.97 kg ha− 1 year− 1 for nitrogen oxidized (NO + NO2 + HNO3 + p-NO3), 5.32 kg ha− 1 year− 1 for nitrogen reduced (NH3 + p-NH4) and 15.77 kg ha− 1 year− 1 for sulfur (SO2 + p-SO4). 70–90% total dry deposition was due to gaseous species deposition. The contribution of dry deposition to the total (wet + dry) was at the level of 60–70% for sulfur and nitrogen (oxidized and reduced), whereas dry chloride deposition contributed 35% to the total. The dry-to-wet deposition ratio of all the studied species was found to be significantly associated with the precipitation amount, with nitrogen species being better and higher correlated. Wet, dry and total depositions measured in Thessaloniki, were compared with other countries of Europe, US and Asia.  相似文献   

4.
This paper reports results of a comparison of two popular rice growth models- Ceres-Rice and ORYZA1N for the same input conditions. Both models use different approaches for simulating growth and yield, are sensitive to climate change parameters, and represent two major schools of crop modelling. A dataset of 32 experiments consisting of 98 treatments was assembled from an extensive literature search. These experiments were conducted over the period of 1980–1993 in diverse Indian locations from 11° N–33° N. The treatments varied in N management, sowing dates, varieties and seasons. The flowering duration in the dataset varied between 37 and 86 days and grain yields between 2587 kg ha–1 and 8877 kg ha–1. Seven treatments from this dataset, one for each variety, were selected for calibration. The genetic coefficients of different varieties used in the analysis for both models were estimated from this short-listed dataset by repeated iterations until a close match between simulated and observed phenology and yield was obtained in these treatments. Similarly 11 treatments with zero or low N applications were used for calibration of initial soil N for different locations. The remaining 80 treatments were used for validation of the models. Both models predicted satisfactorily the trends of leaf area and dry matter growth, grain number, days to flowering and grain yields. Simulated yields were within +15% of the measurements. Considering that the field measurements also generally have 10–15% error and that the treatments widely varied in weather conditions, particularly in temperature, it was concluded that both models are adequate to simulate the effects of climate change on rice yields in diverse agro-environments of India that are free from all pests.  相似文献   

5.
Forest inventories and remote sensing are the two principal data sources used to estimate carbon (C) stocks and fluxes for large forest regions. National governments have historically relied on forest inventories for assessments but developments in remote sensing technology provide additional opportunities for operational C monitoring. The estimate of total C stock in live forest biomass modeled from Landsat imagery for the St. Petersburg region was consistent with estimates derived from forest inventory data for the early 1990s (272 and 269 TgC, respectively). The estimates of mean C sink in live forest biomass also agreed well (0.36 and 0.34 Mg C ha–1 yr–1). Virtually all forest lands were accumulating C in live biomass, however when the net change in total ecosystem C stock was considered, 19% of the forest area were a net source of C. The average net C sink in total ecosystem biomass is quite weak (0.08 MgC ha–1 yr–1 and could be reversed by minor increases in harvest rates or a small decline in biomass growth rates.  相似文献   

6.
Forest inventories and remote sensing are the two principal data sources used to estimate carbon (C) stocks and fluxes for large forest regions. National governments have historically relied on forest inventories for assessments but developments in remote sensing technology provide additional opportunities for operational C monitoring. The estimate of total C stock in live forest biomass modeled from Landsat imagery for the St. Petersburg region was consistent with estimates derived from forest inventory data for the early 1990s (272 and 269 TgC, respectively). The estimates of mean C sink in live forest biomass also agreed well (0.36 and 0.34 Mg C ha–1 yr–1). Virtually all forest lands were accumulating C in live biomass, however when the net change in total ecosystem C stock was considered, 19% of the forest area were a net source of C. The average net C sink in total ecosystem biomass is quite weak (0.08 MgC ha–1 yr–1 and could be reversed by minor increases in harvest rates or a small decline in biomass growth rates.  相似文献   

7.
Precipitation samples were collected by filtrating bulk sampler in Kitakyushu City, Japan, from January 1988 to December 1990. Volume weighted annual mean of pH was 4.93, but the pH distribution indicated that most probable value lay in the range pH 6.0–6.4. Volume weighted annual mean concentrations of major ionic components were as follows; SO 4 2– : 84.2, NO 3 – : 28.1, Cl–: 86.3, NH 4 + : 45.5, Ca2+: 63.3, Mg2+: 27.0, K+: 3.4, Na+: 69.0 µ eq l–1. The highest concentrations of these ionic components were observed in winter and the lowest occurred in the rainy season. The ratio of ex-SO 4 2– /NO 3 – exhibited the lowest ratio in summer, and the highest ratio in winter. Good correlations were obtained between Cl– and Na+, ex-SO 4 2+ and ex-Ca2+, NO 3 – and ex-Ca2+, and NH 4 + and ex-SO 4 2– , respectively. However, no correlation between Cl– and Na+ with Ca2+ was observed. The relationship of H+ with (ex-SO 4 2– + NO 3 – ) - (ex-Ca2+ + NH 4 + ) indicated positive correlation.  相似文献   

8.
Application of nitrate fertilizers on two types of forest soils led to a marked increase in the NO emission rate indicating a large potential for NO production in these soils. The largest fluxes on the fertilized plots were up to 60 ng NO–N m–2 s–1. About 0.35% of the applied nitrogen was lost as NO within about 14 days after fertilization. The fluxes from the unfertilized forest soils were in the range 0.1 to 0.8 ng NO–N m–2 s–1 with a median value of 0.3 ng NO–N m–2 s–1. If this value, obtained during June and August to September, is representative for the growing season (150 days), it corresponds to an annual emission of 0.04 kg NO–N ha–1. This is about 30% of the value obtained for an unfertilized agricultural soil. Because of the large areas occupied by forests in Sweden the flux of NO from forest soils represents a significant contribution to the total flux of NO from soils in Sweden.Earlier observations of equilibrium concentrations for NO have been verified. These were found to range from 0.2 to 2 ppbv for an unfertilized forest soil and up to 170 ppbv for a fertilized soil. At the rural site in Sweden where these measurements were performed the ambient concentrations where found to be less than this equilibrium concentration, and consequently there was generally a net emission of NO.There are still large uncertainties about the global flux of NO from soils. Using direct measurements on three different types of ecosystems and estimates based on a qualitative discussion for the remaining land areas, a global natural source for NO of the order of 1 Tg N a–1 was obtained. If 0.35% of the total annual production of fertilizer nitrogen is lost as NO, fertilization of soils may contribute with 20% to the natural flux from soils.  相似文献   

9.
An experimental study is described of Fe(III)-S(IV) formation constants measured as a function of pH (1–3), ionic strength (0.2–0.5 M) and [Fe(III)] T (2.5–5.0×10–4 M) using a continuous-flow spectrophotometric technique to make observations 160 ms after mixing. Preliminary experiments using pulse-accelerated-flow (PAF) spectrophotometry to measure rate constants on a microsecond timescale are also described. The conditional formation constant at 25 °C can be modeled with the following equation: {ie307-1} where {ie307-2}K 7 andK 8 can be interpreted as intrinsic constants for the coordination of HSO 3 – by FeOH2+ and Fe3+, respectively, but until further evidence is obtained they should be regarded as fitting constants. PAF spectrophotometry showed that the initial reaction of Fe(III) with S(IV) (pH 2.0) is characterized by a second-order rate constant of 4×106 M–1 s–1 which is comparable to rate of reaction of FeOH2+ with SO 4 2– . However, the PAF results should be regarded as preliminary since unexpected features in the initial data indicate that the reaction may be more complex than expected.  相似文献   

10.
Rainwater samples were collected for the monsoon period of 1988 and 1991–1996 at Dayalbagh (Agra), a suburban site situated in semiaridregion. The mean pH was 7.01 ±1.03 well above 5.6, which is the reference pH. Concentration of Ca2+ was observed to be highest followed by Mg2+, NH4 +,SO4 2–, Cl–,NO3 –, Na+, F– and K+. The ratios of SO4 2– + NO3 – andCa2+ + Mg2+ (TA/TC) have been considered as indicatorfor acidity. In the Agra region ratio of TA/TC is quite below 1.0 indicating alkaline nature of rainwater. The lowest value of 0.24 was observed in 1991 likely due to the lowest rain depth of the decade. The highest value of 0.54 was observed in 1996, a year with a large rain depth and increase in line (vehicular traffic) and area sources (population growth). Good correlation between Ca2+ and NO3 –,Ca2+ and SO4 2– andSO4 2– and NO3 –,indicates that wind carried dust and soil play a significant role in neutralization of precipitation acidity.  相似文献   

11.
The soil C balance is determined by the difference between inputs (e.g., plant litter, organic amendments, depositional C) and outputs (e.g., soil respiration, dissolved organic C leaching, and eroded C). There is a need to improve our understanding of whether soil erosion is a sink or a source of atmospheric CO2. The objective of this paper is to discover the long-term influence of soil erosion on the C cycle of managed watersheds near Coshocton, OH. We hypothesize that the amount of eroded C that is deposited in or out of a watershed compares in magnitude to the soil C changes induced via microbial respiration. We applied the erosion productivity impact calculator (EPIC) model to evaluate the role of erosion–deposition processes on the C balance of three small watersheds (∼1 ha). Experimental records from the USDA North Appalachian Experimental Watershed facility north of Coshocton, OH were used in the study. Soils are predominantly silt loam and have developed from loess-like deposits over residual bedrock. Management practices in the three watersheds have changed over time. Currently, watershed 118 (W118) is under a corn (Zea mays L.)–soybean (Glycine max [L.] Merr.) no till rotation, W128 is under conventional till continuous corn, and W188 is under no till continuous corn. Simulations of a comprehensive set of ecosystem processes including plant growth, runoff, and water erosion were used to quantify sediment C yields. A simulated sediment C yield of 43 ± 22 kg C ha−1 year−1 compared favorably against the observed 31 ± 12 kg C ha−1 year−1 in W118. EPIC overestimated the soil C stock in the top 30-cm soil depth in W118 by 21% of the measured value (36.8 Mg C ha−1). Simulations of soil C stocks in the other two watersheds (42.3 Mg C ha−1 in W128 and 50.4 Mg C ha−1 in W188) were off by <1 Mg C ha−1. Simulated eroded C re-deposited inside (30–212 kg C ha−1 year−1) or outside (73–179 kg C ha−1 year−1) watershed boundaries compared in magnitude to a simulated soil C sequestration rate of 225 kg C ha−1 year−1 and to literature values. An analysis of net ecosystem carbon balance revealed that the watershed currently under a plow till system (W128) was a source of C to the atmosphere while the watersheds currently under a no till system (W118 and W188) behaved as C sinks of atmospheric CO2. Our results demonstrate a clear need for documenting and modeling the proportion of eroded soil C that is transported outside watershed boundaries and the proportion that evolves as CO2 to the atmosphere.  相似文献   

12.
Rate constants have been measured for the gas-phase reactions of hydroxyl radical with two halons and three of their proposed substitutes and also with CHClBr-CF3 using the discharge-flow-EPR technique over the temperature range 298–460 K. The following Arrhenius expressions have been derived (units are 10–13 cm3 molecule–1 s–1): (9.3 –0.9 +1.0 ) exp{–(1326±33)/T} for CHF2Br; (7.2 –0.6 +0.7 ) exp{–(1111±32)/T} for CHFBrCF3; (8.5 –0.8 +0.9 ) exp{–(1113±35)/T} for CH2BrCF3; (12.8 –1.2 +1.5 ) exp{–(995±38)/T} for CHClBrCF3. The rate constants at 298 K have been estimated to be <2×10–17 cm3 molecule–1 s–1 for CF3Br and CF2Br—CF2Br. The atmospheric lifetimes due to hydroxyl attack have been estimated to be 5.5, 3.3, 2.8, and 1.2 years for CHF2Br, CHFBr—CF3, CH2Br—CF3 and CHClBr—CF3, respectively.  相似文献   

13.
We present the first application of a multi-stage impactor to study volcanic particle emissions to the troposphere from Masaya volcano, Nicaragua. Concentrations of soluble SO4 2–,Cl–, F–, NO3 –, K+, Na+,NH4 +, Ca2+ and Mg2+ were determined in 11 size bins from 0.07 m to >25.5 m. The near-source size distributions showed major modes at 0.5m (SO4 2–, H+,NH4 +); 0.2 m and 5.0 m (Cl–) and 2.0–5.0 m(F–). K+ and Na+ mirrored the SO4 2– size-resolvedconcentrations closely, suggesting that these were transported primarily asK2SO4 and Na2SO4 in acidic solution, while Mg2+ andCa2+ presented modes in both <1 m and >1 m particles. Changes in relative humidity were studied by comparing daytime (transparent plume) and night-time (condensed plume) results. Enhanced particle growth rates were observed in the night-time plume as well as preferential scavenging of soluble gases, such as HCl, by condensed water. Neutralisation of the acidic aerosol by background ammonia was observed at the crater rim and to a greater extent approximately 15 km downwind of the active crater. We report measurements of re-suspended near-source volcanic dust, which may form a component of the plume downwind. Elevated levels ofSO4 2–, Cl–, F–,H+, Na+, K+ and Mg2+ were observed around the 10 m particle diameter in this dust. The volcanic SO4 2– flux leaving the craterwas 0.07 kg s–1.  相似文献   

14.
The Denitrification-Decompostion (DNDC) model was used to estimate the impact of change in management practices on N2O emissions in seven major soil regions in Canada, for the period 1970 to 2029. Conversion of cultivated land to permanent grassland would result in the greatest reduction in N2O emissions, particularly in eastern Canada wherethe model estimated about 60% less N2O emissions for thisconversion. About 33% less N2O emissions were predicted for a changefrom conventional tillage to no-tillage in western Canada, however, a slight increase in N2O emissions was predicted for eastern Canada. GreaterN2O emissions in eastern Canada associated with the adoption of no-tillage were attributed to higher soil moisture causing denitrification, whereas the lower emissions in western Canada were attributed to less decomposition of soil organic matter in no-till versus conventional tilled soil. Elimination of summer fallow in a crop rotation resulted in a 9% decrease in N2O emissions, with substantial emissions occurringduring the wetter fallow years when N had accumulated. Increasing N-fertilizer application rates by 50% increased average emissions by 32%,while a 50% decrease of N-fertilizer application decreased emissions by16%. In general, a small increase in N2O emissions was predicted when N-fertilizer was applied in the fall rather than in the spring. Previous research on CO2 emissions with the CENTURY model (Smith et al.,2001) allowed the quantification of the combined change in N2O andCO2 emissions in CO2 equivalents for a wide range of managementpractices in the seven major soil regions in Canada. The management practices that have the greatest potential to reduce the combined N2O andCO2 emissions are conversion from conventional tillage to permanent grassland, reduced tillage, and reduction of summer fallow. The estimated net greenhouse gas (GHG) emission reduction when changing from cultivated land to permanent grassland ranged from 0.97 (Brown Chernozem) to 4.24 MgCO2 equiv. ha–1 y–1 (BlackChernozem) for the seven soil regions examined. When changing from conventional tillage to no-tillage the net GHG emission reduction ranged from 0.33 (Brown Chernozem) to 0.80 Mg CO2 equiv. ha–1 y–1 (Dark GrayLuvisol). Elimination of fallow in the crop rotation lead to an estimated net GHG emission reduction of 0.43 (Brown Chernozem) to 0.80 Mg CO2 equiv.ha–1 y–1 (Dark Brown Chernozem). The addition of 50% more or 50% less N-fertilizer both resulted in slight increases in combined CO2 and N2O emissions. There was a tradeoff in GHG flux with greaterN2O emissions and a comparable increase in carbon storage when 50% more N-fertilizer was added. The results from this work indicate that conversion of cultivated land to grassland, the conversion from conventional tillage to no-tillage, and the reduction of summerallow in crop rotations could substantially increase C sequestration and decrease net GHG emissions. Based on these results a simple scaling-up scenario to derive the possible impacts on Canada's Kyoto commitment has been calculated.  相似文献   

15.
This paper presents dry deposition flux and deposition velocity of atmospheric particles on white marble and red stone at Dayalbagh, a suburban site of semi arid region, which is 10 km away from the industrial sector of the Agra city where due to agricultural practices vegetation predominates. The wind speed at Agra is mostly in the range of 1–2 m s–1. The atmospheric calm conditions at Agra in summer, monsoon, and winter seasons are 47%, 35%, and 76%, respectively. Industrial areas of the city are away from Dayalbagh and are located in the NE, E, SE, and SW sectors. The main industrial activities, which are in operation in Agra city and its outskirts, are foundry and forging industry. The other industrial activities in Agra are rubber processing, lime oxidation and pulverization, chemicals, engineering and brick refractory kilns. Dry deposition samples were collected on dry days on white marble and red stone (0.224 m × 0.224 m × 0.02 m) using surface washing method. Both slabs were fixed to an iron stand (1.5 m height) at an angle of about 80 from the horizontal and exposed for 24 h on the roof of the faculty building. The order of deposition flux on white marble is NH4+ > Mg2+ > Ca2+ > Na+ > Cl– > K+ > NO3– > SO42– > F– and that on red stone is NH4+ > Mg2+ > Ca2+ > SO42– > Na+ > NO3– > K+ > F– > Cl–. Average dry deposition flux of major ions varies from 3.4 to 128.5 M m–2 d–1. The sum of major cations on white marble and red stone are 516.4 and 450.4 eq m–2 d–1, respectively while sum of major anions are 425.3 and 400.4 eq m–2 d–1 on white marble and red stone, respectively. Higher deposition of all ions was observed when wind blows from NE as most of the Agra Iron foundries and Ferozabad glass industries lie in this direction. The mean values of dry deposition velocity of ions vary between 0.22 cm s–1 to 1.49 cm s–1. Deposition velocity for all ions is higher on white marble than red stone inspite of rougher surface of red stone as compared to white marble. This could be due to the chemical nature of white marble, which is made of dolomite and hence adds significant amount of ions by dissolution during washing. Seasonally the deposition velocity was highest in winter.  相似文献   

16.
The absolute rate constants for the gas-phasereactions of the NO3 radical with a series ofaldehydes such as acetaldehyde, propanal, butanal,pentanal, hexanal and, heptanal were measured overthe temperature range 298–433 K, using a dischargeflow system and monitoring the NO3 radical byLaser Induced Fluorescence (LIF).The measured rate constants at 298 K for thereaction of NO3, in units of 10–14 cm3molecule–1 s–1, were as follows:acetaldehyde 0.32 ± 0.04, propanal 0.60 ± 0.06, butanal 1.46± 0.16, pentanal 1.75 ±0.06, hexanal 1.83 ± 0.36, and heptanal 2.37 ±0.42. The proposed Arrhenius expressions arek1 = (6.2 ± 7.5) × 10–11 exp[–(2826 ± 866)/T] (cm3 molecule–1s–1),k2 = (1.7 ± 1.0) × 10–11 exp[–(2250 ± 192)/T] (cm3 molecule–1s1), k3 =(7.6 ± 9.8) × 1011 exp[–(2466 ± 505)/T] (cm3 molecule–1s–1),k4 = (2.8 ± 1.4) × 10–11 exp[–(2189 ± 156)/T] (cm3 molecule–1s–1), k5 = (7.0 ± 1.8) ×10–11 exp [–(2382 ± 998)/T](cm3 molecule–1 s–1), andk6 = (7.8 ± 1.0) × 10–11 exp[–(2406 ± 481)/T](cm3 molecule–1 s–1).Tropospheric lifetimes for these aldehydes werecalculated at night and during the day for typicalNO3 and OH average concentrations and showed thatboth radicals provide an effective tropospheric sinkfor these compounds and that the night-time reactionwith the NO3 radical can be an important, if notdominant, loss process for these emitted organics andfor NO3 radicals.  相似文献   

17.
The kinetics of the aqueous phase reactions of NO3 radicals with HCOOH/HCOO– and CH3COOH/CH3COO– have been investigated using a laser photolysis/long-path laser absorption technique. NO3 was produced via excimer laser photolysis of peroxodisulfate anions (S2O 8 2– ) at 351 nm followed by the reactions of sulfate radicals (SO 4 – ) with excess nitrate. The time-resolved detection of NO3 was achieved by long-path laser absorption at 632.8 nm. For the reactions of NO3 with formic acid (1) and formate (2) rate coefficients ofk 1=(3.3±1.0)×105 l mol–1 s–1 andk 2=(5.0±0.4)×107 l mol–1 s–1 were found atT=298 K andI=0.19 mol/l. The following Arrhenius expressions were derived:k 1(T)=(3.4±0.3)×1010 exp[–(3400±600)/T] l mol–1 s–1 andk 2(T)=(8.2±0.8)×1010 exp[–(2200±700)/T] l mol–1 s–1. The rate coefficients for the reactions of NO3 with acetic acid (3) and acetate (4) atT=298 K andI=0.19 mol/l were determined as:k 3=(1.3±0.3)×104 l mol–1 s–1 andk 4=(2.3±0.4)×106 l mol–1 s–1. The temperature dependences for these reactions are described by:k 3(T)=(4.9±0.5)×109 exp[–(3800±700)/T] l mol–1 s–1 andk 4(T)=(1.0±0.2)×1012 exp[–(3800±1200)/T] l mol–1 s–1. The differences in reactivity of the anions HCOO– and CH3COO– compared to their corresponding acids HCOOH and CH3COOH are explained by the higher reactivity of NO3 in charge transfer processes compared to H atom abstraction. From a comparison of NO3 reactions with various droplets constituents it is concluded that the reaction of NO3 with HCOO– may present a dominant loss reaction of NO3 in atmospheric droplets.  相似文献   

18.
Henry's law constants KH (mol kg–1 atm–1) for the reaction HOCl(g)=HOCl(aq) near room temperature, literature data for the associated enthalpy change, and solubilities of HOCl in aqueous H2SO4 (46 to 60 wt%) at temperatures relevant to the stratosphere (200 KT230 K) are shown to be thermodynamically consistent. Effective Henry's law constants [H*=mHOCl/pHOCl, in mol kg–1 atm–1] of HOCl in aqueous H2SO4 are given by: ln(H*)=6.4946–mH2SO4(–0.04107+54.56/T)–5862 (1/To–1/T) where T(K) is temperature and To=298.15K. The activity coefficient of HOCl in aqueous H2SO4 has a simple Setchenow-type dependence upon H2SO4 molality.  相似文献   

19.
Absolute rate coefficient measurements have been carried out for the reactions of Cl atoms with propene and a series of 3-halopropenes, at room temperature (298 ± 2) K using a newly constructed laser photolysis-resonance fluorescence (PLP-RF) system. The rate coefficients obtained (in units of cm3 molecule–1 s–1) are: propene (1.40± 0.24) ×10–10, 3-fluoropropene (4.92 ± 0.42) ×10–11, 3-chloropropene (7.47 ± 1.50) × 10–11, 3-bromopropene (1.23± 0.14) ×10–10 and 3-iodopropene (1.29± 0.15) ×10–10. In order to test this new system, the reactions of Cl atoms with acetone and isoprene have also been studied and compared with data previously reported. The rate coefficients determined at room temperature for these last two reactions are (2.93 ± 0.20) ×10–12 cm3 molecule–1 s– 1 and (3.64± 0.20)×10–10 cm3 molecule–1 s–1, respectively. The measured values were independent of pressure over the range 20–200 Torr. The influence of the different halogen atoms substituents on the reactivity of these alkenes with Cl atoms as well as the atmospheric implications of these measurements are studied and discussed for the first time in this work and compared with the reactivity with NO3 and OH radicals.  相似文献   

20.
Rainwater samples were collected in Irbid city using 24 hour sampling periods from December 1996 to April 1998. All samples were analyzed for major cations (Na+, K+, Ca2+ and Mg2+), major anions (Cl–, NO3 – and SO4 2–) and pH. High levels of Ca2+ and SO4 2– were observed. Together, Ca2+ and SO4 2– made up more than 52.4% of the total ion mass, while Ca2+ alone contributed over 39.0% of the total cation. The majority of the rain samples collected had pH values higher than 5.6. The average pH was 6.4±0.9. High values of pH are attributed to the neutralization by natural alkaline local dusts which contain large fractions of calcite. Correlation and mineralogical analyses indicated that Ca2+, K+ and fractions of Na+, SO4 2– and Mg2+ are of crustal origin. Results of the present study suggested that the atmospheric composition in the city is strongly influenced by natural sources rather than anthropogenic.  相似文献   

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