恒电荷土壤和可变电荷土壤动电性质的研究 Ⅱ.阴离子吸附和pH的影响

本工作研究了阴离子吸附和ＰＨ对恒电荷土壤（黄棕壤和黑土）和可变电荷土壤（砖红壤）动电性质的影响。结果表明,砖红壤吸附不同阴离子后的ζ电位随ＰＨ升高由正电位移至负电位,在ζ电位－ＰＨ曲线上均有一个等电点（ＩＥＰ）在ＰＨ３．５～８之间,相同ＰＨ升高由正电红壤的ζ电位随吸附阴离子的负移顺序是ＨＰＯ４＾２－〉Ｆ＾－〉ＳＯ４＾２－〉Ｃｌ＾－〉ＮＯ３＾－。作为恒电荷土壤的黄棕壤和黑土,在不同电解发质溶液中的ε     

The Applicability of the Local and International Water Quality Guidelines to Al-Gassim Region of Central Saudi Arabia

The quality of 109 water samples, comprised of 70 drinking waterand 39 irrigation water samples, in Al-Gassim Region of SaudiArabia was investigated with respect to total dissolved salts(TDS), electric conductivity (EC), pH, total hardness and themajor cations (Ca²⁺, Mg²⁺, Na⁺ and K⁺) andanions (Cl^-, SO₄ ^2-, NO₃ ^-,F^- andHCO₃ ^-) beside coliform bacteria as an indicator offaecal contamination.The concentrations of TDS varied widely, from 109 to 6995 mgL^-1, with a mean of 1427 mg L^-1. Of the 109 watersamples examined, 81 (74.3%) comply with the maximumpermissible drinking water limits set by the local and international standards and guidelines and 28 (25.7%) were abovethe limits of these standards. The concentrations of the cationsand anions (with the exception of NO₃ ^- and F^-)follow, more or less, a trend similar to TDS. NO₃ ^- concentrations (range 0–30 mg L^-1) comply with the limitof 50 mg L^-1 NO₃ ^- as the highest tolerableNO₃ ^- content. The concentrations of F^- indrinking water (range 0.2–1.5 mg L^-1) are alarming since88% of samples were below the lower permissible limit of 0.6 mgL^-1 set by SASO (1984), the guideline of the WHO is 1.5 mgL^-1 while the EEC maximum concentration lies within the range 0.7–1.5 mg L^-1. Microbiological analyses showednegative coliform tests, which confirms that they are devoid ofany faecal contamination.     

采前营养液处理对水培小白菜硝酸盐积累的影响

开展了在采收前减少小白菜营养液中的氮量或在去除硝态氮的基础上加入渗调离子以试图降低小白菜的硝酸盐积累的试验。结果表明,在去除营养液中的硝态氮后,在营养液中加入Cl-、SO42-、苹果酸根离子、山梨酸根离子、乙酸根离子是降低溶液培养小白菜硝酸盐积累的有效措施,但处理后采收的时间不可推迟太久。而只减少营养液中氮肥用量会使产量迅速下降,硝酸盐含量降低却缓慢,加入渗调离子可缓解因去除氮肥引起的小白菜产量的下降。     

伴随阴离子对马铃薯种植冲击土中钾素固持与淋溶的影响

A column study was carried out to assess the influence of accompanying anions on potassium (K) leaching at potato growing sites with different soil textures (sandy loam and clay loam) in northwestern India. Potassium was applied in the top 15 cm layer of soil column at 30 and 60 mg K kg^-1 through different sources having different accompanying anions (Cl^-, SO₄^2-, NO₃^- and H₂PO₄^-). Maximum K was retained in the top 0--15 cm layer with a sharp decrease in K content occurring in 15--30 cm layer of the soil column. The trend was similar for both levels of applied K as well as frequency of leaching and soil type. The decrease of K content in soil column after four leaching events was maximum in case of Khanaura sandy loam, while only minor decrease was observed in Hundowal clay loam when K was applied at 60 mg K kg^-1, indicating higher potential of clay rich soil to adsorb K. In general, the K leaching in presence of the accompanying anions followed the order of SO₄^2- ≤ H₂PO₄^2- < NO₃^- = Cl^-. Highest 1 mol L^-1 CH3COONH4-extractable K was retained when K was applied along with SO42- and H2PO4- anions, and the least was retained when accompanying anion was Cl^-1. The influence of anions was more pronounced in the light textured soil and at high amounts of K application. Higher levels of K application resulted in higher losses of K, especially in sandy loam soil as observed from the leachate concentration. Among the different K sources, the maximum amount of K leaching was noticed in the soil column amended with KCl. After four leachings, the maximum amount of K leached out was 6.40 mg L^-1 in Hundowal clay loam and 9.29 mg L^-1 in Khanaura sandy loam at 60 mg K kg^-1 of soil application through KCl. These concentrations were lower than the recommended guideline of the World Health Organisation (12.00 mg L^-1).     

恒电荷土壤与可变电荷土壤对Cl~-和NO_3~-吸附的差异及其机理

对 3种可变电荷土壤和 4种恒电荷土壤在不同 pH、不同浓度、不同相伴阴阳离子下混合体系中Cl-和NO3-的吸附进行了测定。结果表明 ,在Cl-和NO3- 共存体系中 ,Cl-比例增大使可变电荷土壤Na+吸附量及OH-释放量增加 ,而对恒电荷土壤影响不大。Cl-和NO3-吸附量随平衡Cl-和NO3-浓度增加而增大 ,随pH升高而减少。但恒电荷土壤在上述各种条件下对Cl-和NO3-吸附均相同 ,而可变电荷土壤对Cl-吸附量大于NO3-的吸附量 ;NO3-、Cl-的选择系数为 0.51～0.78,Cl-和NO3-的相对吸附量分别为56.9%和 43.1%。在不同相伴阳离子下 ,可变电荷土壤平衡溶液Cl-/NO3-比值均小于 1,且为Na+K+Ca2+Mg2+Fe3+;而恒电荷土壤Cl-/NO3-比值为 1左右 ,且不受阳离子类型的影响。由此认为 ,Cl-和NO3-在两类土壤中均以电性吸附为主 ,恒电荷土壤对Cl-和NO3-的亲合力及吸附机理相同 ;而可变电荷土壤对Cl-的亲合力 NO3- ,Cl-存在着专性吸附     

Increase in Cation Adsorption Induced by Surface Complexation of Sulfate on Andisols and Prediction by “Four-Plane Model”

Abstract

The “Four-plane model” is one of the surface complexation models developed for analyzing the electrostatic charge of synthetic oxides. This model which was applied to the B horizon of Andisols, was equilibrated with an electrolyte solution containing KCl, KNO₃, K₂SO₄ in the concentration range of 0.0033, 0.01, 0.033, 0.1 M, and pH range of 2 to 11. The amounts of NO₃ ^-, Cl^-, SO₄ ^2-, and K⁺ adsorbed were determined from the products remaining in the liquid phase. The increase in the pH value results in the increase of K⁺ adsorption, and decrease of anion adsorption. The increase in the equilibrium concentration increased both K⁺ and anion adsorption. The parameters of the model were determined by measurements and the iterative method. The model have a good agreement between calculated and measured values of cation and anion adsorption. Among the anion species, the amount of adsorbed anions was in the order of SO₄ ^2-?Cl^->NO₃ ^-. The differences in the degree of adsorption were mainly associated with the differences in the equilibrium constants of surface complexation. The surface complexation of the anions produced a negative charge and increased cation adsorption. The degree of surface complexation was most significant in the K₂SO₄ solution, and the phenomenon was considered to be important not only for anion adsorption but also for cation adsorption on Andisols.     

Adsorption features of Cu(II), Pb(II), and Zn(II) by an ordinary chernozem from nitrate,chloride, acetate,and sulfate solutions

The effect of Cl^?,SO ₄ ^2? , CH₃COO^?, and NO ₃ ^? anions on the adsorption of copper, lead, and zinc by an ordinary chernozem has been studied. The effect of the anions on the adsorption of Cu²⁺, Pb²⁺, Zn²⁺ ions is significant but uncertain. It has been shown that the attendant anions affect the shape of the adsorption isotherms, which are described by the Langmuir, Freundlich, or Henri equations. The constants of the adsorption from a nitrate solution calculated from the Langmuir equation (K _L) decrease in the following order: Cu²⁺ > Pb²⁺ >> Zn²⁺. The values of the maximum adsorption (C _max) decrease in the following order: Cu²⁺ ≥ Zn²⁺ > Pb²⁺ for acetate solutions and in the series Pb²⁺ > Zn²⁺ ≥ Cu²⁺ for nitrate solutions. The values of the Henry constants (K _H) calculated for the adsorption of the same cations from chloride solutions decrease in the same order as the values of K _L. The CH₃COO^? anion has the highest effect on the constant values. The NO ₃ ^? and Cl^? anions “switch their places” depending on the attendant cation, but their effect is always lower than that of the acetate anion. The values of C _max for copper and zinc are most affected by the CH₃COO^? anion, and the adsorption of zinc is most affected by the Cl^? and NO ₃ ^? anions. The assessment of the mobility of the adsorbed cations from the extraction with ammonium acetate (pH 4.8) has shown that the content of the desorbed metals is always lower than the content of the adsorbed cations and varies from 0.025 to 83%. According to their mobility, the adsorbed metals form the following order: Zn²⁺ > Pb²⁺ > Cu²⁺. The effect of the attendant anions on the extractability of the adsorbed cations decreases in the following order: chlorides > sulfates > acetates > nitrates.     

Effects of Forms and Rates of Zinc Fertilizers on Cadmium Concentrations in Two Cultivars of Maize

Abstract

A pot experiment was conducted to investigate the effects of three soluble zinc (Zn) fertilizers on cadmium (Cd) concentrations in two genotypes of maize (Zea mays): Jidan 209 and Changdan 374. Zinc fertilizers were added to soil at four levels: 0, 80, 160, and 240 mg kg^?1 soil as nitrate [Zn(NO₃)₂], chloride (ZnCl₂), and sulfate (ZnSO₄). Cadmium nitrate [Cd(NO₃)₂] was added to all the treatments at a uniform rate equivalent to 10 mg kg^?1 soil. The biomass of maize plants was increased with the application of three zinc fertilizers, of which Zn(NO₃)₂ yielded more than others. Under ZnCl₂ treatment, plant growth was promoted at the lower level and depressed at the higher one. All the three fertilizers decreased Cd concentration in shoots in comparison with treatments without Zn, but there were variations with different forms, especially in plants treated with Zn(NO₃)₂, which had the minimal value. The orders of average Cd concentration in shoots with different zinc fertilizers were ZnSO₄>ZnCl₂>Zn(NO₃)₂ for Jidan 209 and ZnCl₂>ZnSO₄>Zn(NO₃)₂ for Changdan 374, respectively (P<0.001). There was no significant difference between ZnSO₄ and ZnCl₂ treatments. The lowest Cd concentration in shoots was found in the 80‐mg‐kg^?1 soil or 160‐mg‐kg^?1 soil treatment. Cadmium concentration in roots in the presence of ZnCl₂ was the lowest and under ZnSO₄ the highest. The mechanism involved needs to be studied to elucidate the characteristics of complexation of Cl^? and SO₄ ^2? with Cd in plants and their influence on transfer from roots to shoots.     

Comparison of the Chemical Composition of Precipitation on the Western and Eastern Coasts of Korea

Precipitation samples were collected at two coastal sites on the Korean Peninsula, Kangwha on the western coast and Yangyang on the eastern coast, from September 1991 to February 1997. The samples were analyzed for concentrations of major ions, in addition to pH and electrical conductivity. The annual volume-weighted mean pH values were 4.89 and 5.05 at Kangwha and Yangyang, respectively. The pH was generally lower at Kangwha than that at Yangyang, especially during the winter, because of reduced neutralizing inputs and greater acid inputs in winter. Dominant ions were different with NH₄ ⁺ and SO₄ ^2- most important at Kangwha and Na⁺ and Cl^- at Yangyang. Neglecting sea salt components, nss-SO₄ ^2- and NO₃ ^- were important anions and nss-Ca²⁺ and NH₄ ⁺ were important cations at both sites. Concentrations of these ions were 1.2–1.6 times higher at Kangwha than at Yangyang. Annual mean concentrations of these ions varied little during the study, while larger seasonal variations were observed. Annual mean nss-SO₄ ^2-/NO₃ ^- ratios at Kangwha and Yangyang were 2.8 and 2.6. The 5 yr annual mean values of nss-SO₄ ^2-/NO₃ ^- showed no trend at Kangwha but a decreasing tendency at Yangyang. The decreasing trend is similar to the decreasing trend in emissions of SO₂/NO_x in South Korea. Regional differences in chemical composition between Kangwha and Yangyang appear to be associated with long-range transport of acidic gases and alkaline dust originated from other regions.     

Chemical Composition of Precipitation in Beijing Area, Northern China

Variations of anions (SO₄ ^2-, NO₃ ^-,NO₂ ^-, Cl^- and F^-),cations (K⁺,Na⁺, Ca²⁺, Mg²⁺ and ⁺) and pH values in precipitation, througfall and stemflow samples collected overa four-year period (1995–1998) in Beijing (two sitesZhongguancun and Mangshan) are presented. The annualvolume-weighted range of pH values were 6.57–7.11 inprecipitation, 5.46–6.86 in thoughfall and 5.32–6.41 instemflow. The fominant anion was , while Ca⁺and NH₄ ⁺ were the main cations in precipitation,throughfall and stemflow. Most of ion concentrations with precipitation, throughfall and stemflow volume showed negative correlation, except for some ones. Significant correlationvalues were also found between ions (SO₄ ^2-,NO₃ ^-, Cl^-, F^-, Ca²⁺,Mg²⁺ andNa⁺) in precipitation, throughfall and stemflow indicatedthe common sources of these ions such as coal combustion,automobile emission and fertilizers application. Compared toprecipitation, there was an increased ion concentration inthroughfall or in stemflow. Changes of ion concentrations werein Quercus liatungensis Koiz. and Pinus tabulaefornisCarr. throughfall (or stemflow) because of different crown andbark qualities of tree species.     

阴离子对可变电荷土壤吸附铜离子的影响机理

根据NO-3、Cl-和SO24-对可变电荷土壤和恒电荷土壤吸附Cu2+的影响的比较,探讨了阴离子对可变电荷土壤吸附Cu2+的影响机理。结果表明,当3种阴离子的浓度相同时,在SO24-体系中铁质砖红壤对Cu2+的吸附率较在NO3-和Cl-体系中大得多,而在浓度相同的3种阴离子体系中,黄棕壤对Cu2+的吸附率相差不大。在离子强度相近的NaCl体系中,砖红壤对Cu2+的吸附率相近。在3种阴离子体系中,随着pH升高,砖红壤对Cu2+的吸附率均增大;但在NO-3体系和Cl-体系中Cu2+的吸附率相近;而在SO24-体系中Cu2+的吸附率最大。随着Na2SO4浓度的增大,铁质砖红壤和砖红壤对Cu2+的吸附率减小。但在0.005 mol L-1和0.05 mol L-1Na2SO4体系中,Cu2+的吸附率大于在不含Na2SO4的体系中者。而在0.5 mol L-1Na2SO4体系中,Cu2+吸附率小于在不含Na2SO4体系中者。在3种浓度的Na2SO4体系中,黄棕壤对Cu2+的吸附率均小于在不含Na2SO4体系中者。总之,阴离子可通过离子强度、专性吸附和形成离子对影响土壤对Cu2+的吸附。在可变电荷土壤中,阴离子对Cu2+吸附的影响机理较在恒电荷土壤中复杂得多。     

Effect of an attendant anion on the balance of cations in the soil-solution system with an ordinary chernozem as an example

The effect of different anions on the balance of heavy metal cations in the soil-solution system has been assessed under model laboratory conditions. It has been found that the uptake of the Cu, Zn, and Pb cations by an ordinary chernozem from solutions of different salts is accompanied by the displacement of the exchangeable cations to the solution in the following order: Ca²⁺ > Mg²⁺ > Na⁺ > K⁺. The sum of the displaced exchangeable cations in most cases exceeds the amount of the adsorbed heavy metal cations. According to the effect of the anions on the displacing capacity of the metal cations, the following series are formed: for copper, SO ₄ ^2? ? Cl^? > OAc^? > NO ₃ ^? ; for lead, Cl^? ? NO ₃ ^? > OAc^?; and, for zinc, SO ₄ ^2? ? Cl^? ? OAc^? > NO ₃ ^? .     

电解质对酸性土壤铝的溶解及铝形态在土壤溶液中的分布的影响

KCl, CaCl₂, NH₄Cl, NaCl, K₂SO₄ and KF solutions were used for studying the effects of cations and anions on the dissolution of aluminum and the distribution of aluminum forms respectively. Power of exchanging and releasing aluminum of four kinds of cations was in the decreasing order Ca²⁺ >K⁺ >NH₄⁺ >Na⁺. The dissolution of aluminum increased with the cation concentration. The adsorption affinity of various soils for aluminum was different. The aluminum in the soil with a stronger adsorption affinity was difficult to be exchanged and released by cations. The Al-F complexes were main species of inorganic aluminum at a low concentration of cations, while Al³⁺ became major species of inorganic aluminum at a high concentration of cations. The results on the effect of anions indicated that the concentrations of total aluminum, three kinds of inorganic aluminum (Al³⁺, Al-F and Al-OH complexes) and organic aluminum complexes (Al-OM) when SO₄^2- was added into soil suspension were lower than those when Cl^- was added. The dissolution of aluminum from soils and the distribution of aluminum forms in solution were affected by the adsorption of F^- on the soil. For soils with strong affinity for F^-, the concentrations of the three inorganic aluminum species in soil solution after addition of F^- were lower than those after addition of Cl^-; but for soils with weak affinity for F^-, the concentrations of Al³⁺ and Al-OM were lower and the concentrations of Al-F complexes and total inorganic aluminum after addition of F^- were higher than those after addition of Cl^-. The increase of F^- concentration in soil solution accelerated the dissolution of aluminum from soils.     

Intercomparison of snow Sampling and Analysis Within the Alpine-Wide Snowpack Investigation (SNOSP)

In order to investigate the seasonal and geographical distribution of snow concentrations anddeposition fluxes of environmentally relevant ionic species in the Alps, the international programSNOSP was initiated. In the framework of this program, intercomparisons of snow samplingtechniques and analytical methods to determine the ionic species C1^-, NO ₃ ^- ,SO ₄ ^2- , K⁺, Na⁺, NH4 ⁺, Mg²⁺, and Ca²⁺, as well as the pH and the specificconductivity were performed. The concentrations of these species in the snow samples collectedin the SNOSP program varied by orders of magnitude with, e.g., concentrations of NO ₃ ^- , SO ₄ ^2- , and NH4 ⁺ ranging from 0.2-60, 0.2-90, and 0.1-60 µeq L^-1,respectively. The intercomparisons revealed a reasonable agreement of the determinations of thespecies Cl^-, NO ₃ ^- , SO ₄ ^2- , Na⁺, and NH4 ⁺ in snow. Results were less satisfactory for K⁺, Mg²⁺, Ca²⁺,and H⁺, mainly due to the very low concentrations. In conclusion, recommendations areformulated for the reliable derivation of chemical inventories from snow packs.     

Does the potential ammonium fixation of soils have an impact on the optimum nitrogen fertilizer rate?

Field experiments were conducted to determine the effect of nitrogen (N) fertilizer forms and doses on wheat (Triticum aestivum L.) on three soils differing in their ammonium (NH₄) fixation capacity [high = 161 mg fixed NH₄-N kg^?1 soil, medium = 31.5 mg fixed NH₄-N kg^?1 soil and no = nearly no fixed NH₄-N kg^?1 soil]. On high NH₄⁺ fixing soil, 80 kg N ha^?1 Urea+ ammonium nitrate [NH₄NO₃] or 240 kg N ha^?1 ammonium sulfate [(NH₄)₂SO₄]+(NH₄)₂SO₄, was required to obtain the maximum yield. Urea + NH₄NO₃ generally showed the highest significance in respect to the agronomic efficiency of N fertilizers. In the non NH₄⁺ fixing soil, 80 kg N ha^?1 urea+NH₄NO₃ was enough to obtain high grain yield. The agronomic efficiency of N fertilizers was generally higher in the non NH₄⁺ fixing soil than in the others. Grain protein was highly affected by NH₄⁺ fixation capacities and N doses. Harvest index was affected by the NH₄⁺ fixation capacity at the 1% significance level.     

Chemical Composition of Rainwater Near Two Historical Monuments The Thann Collegiate (Alsace,France) and the Tours Cathedral (Indre et Loire,France)

In the present study, included within the framework of a Franco-German Research Program for Conservation of HistoricalMonuments, the chemical composition of rainwater was investigated in Thann (Alsace, France) and in Tours (Indre etLoire, France) between 1992 and 1993. A total of 78 and 24samples, respectively, were collected, near the Thann collegiateand the Tours cathedral on a weekly basis and analysed for Cl^-, NO₃ ^-, SO₄ ^2-, Na⁺, NH₄ ⁺, K⁺, Mg²⁺ and Ca²⁺. Results showpH ranged from 3.60 to 6.58 and from 5.49 to 7.01 for Thann andTours, respectively. In Thann, SO₄ ^2- is the major anion and rainwater acidity is neutralised by compounds ofterrigenic origin which come from the soil of the upper Rhinevalley (Ca²⁺; ‘loess’) and the potash mines of Alsace. In Tours, SO₄ ^2- is also the major anion and the acidity is neutralised partially by atmospheric ammonia and partially by compounds of terrigenic origin and by dust fromthe erosion of the cathedral and the works of restoration, in the form of CaCO₃.     

THE EFFECT OF NITROGEN SOURCES ON YIELD AND QUALITY OF SALAD ROCKET GROWN IN DIFFERENT MONTHS OF THE YEAR

The effects of months of the year and nitrogen (N) sources on salad rocket (Eruca sativa Mill.) yield, quality, and nitrate accumulation was investigated during the years 2002 and 2003. In both years, seeds were sown on the first day of April, May, June, July, August and September. Three different nitrogen sources were used: farmyard (cattle) manure (100 tonnes·ha^?1), calcium nitrate [Ca(NO₃)₂]-15.5% N (150 kg N·ha^?1) and ammonium sulfate [(NH₄)₂SO₄)]-21% N (150 kg N·ha^?1). Yield, leaf color, dry matter, vitamin C and total glucosinolate content and nitrate accumulation was assessed. Growing months affected all the assessed parameters significantly both years, with the exception of hue angle in 2003, whereas nitrogen source only influenced yield and nitrate accumulation in 2003. In both years the highest yield was obtained in April, but vitamin C and total glucosinolate contents were higher during summer months, and leaves were slightly darker colored. Chemical fertilizers increased the yield compared to farmyard manure; however, they also increased nitrate accumulation slightly, without any significant difference between them. Nitrate accumulation never exceeded 300 mg kg^?1 fresh weight (FW), which is well below the acceptable daily intake of 3.7 mg nitrate per kg^?1 bodyweight set by European Commission's Scientific Committee on Food.     

Sequencing Zerovalent Iron Treatment with Carbon Amendments to Remediate Agrichemical-Contaminated Soil

Agrichemical spills and discharges to soil can cause point-source contamination of surface and ground waters. When high contaminant concentrations inhibit natural attenuation in soils, chemical treatments can be used to promote degradation and allow application of treated soils to agricultural lands. This approach was used to remediate soil containing >650 mg atrazine, >170 mg metolachlor and >18,000 mg nitrate kg^?1. Results indicated a decrease in metolachlor concentration to <1 mg kg^?1 within 95 days of chemical treatment with zerovalent iron (Fe⁰, 5% w/w) and aluminum sulfate (Al₂(SO₄)₃, 2% w/w) but after one year >150 mg atrazine and >7000 mg nitrate kg^?1 remained. Laboratory experiments confirmed that subsequent additions of sucrose (table sugar) to the chemically pretreated soil promoted further reductions in atrazine and nitrate concentrations. Field-scale results showed that adding 5% (w/w) sucrose to windrowed and pretreated soil significantly reduced atrazine (<38 mg kg^?1) and nitrate (<2,100 mg kg^?1) concentrations and allowed for land application of the treated soil. These results provide evidence that zerovalent iron in combination with Al₂(SO₄)₃ and sucrose can be used for on-site, field-scale treatment of pesticide- and nitrate-contaminated soil.     

Elemental and Base Anions Deposition in the Snow Cover of North-Eastern Estonia

Snow samples from 18 sites in Estonia were collected in February and March 1996 after 72–110 days of permanent snow cover. Three snow layers corresponding to different snow accumulation periods were separated in each sampling site. Snow water samples were analysed for sulphate (SO₄ ^2-), nitrate (NO₃ ^-), and chloride (Cl^-) ions and elemental composition. Deposition fluxes of 27 chemical species were used for factor, cluster and correlation analysis. The effects of cement dust, oil shale fly ash, sulphur dioxide and chlorine from emissions of thermal power plants were distinguished. A large number of trace metals are strongly correlated with each other (R > 0.8) and with macro-components (except NO₃ ^-), which refers to a common origin, identified as the mineral part of oil shale. Deposition fluxes of Ca, Mg, SO₄ ^2- and a number of mineral components exceed near the power plants 1–2 decimal orders the background value. The deposition fluxes in forested sites are up to 2 times higher than in open land sites. This difference may be caused by more efficient turbulent transfer over rougher surface. It is suggested, that NO₃ ^- and Zn originate mainly and Pb, Cd and Cu partially from non-local or diffuse sources (traffic, domestic heating, far transport). The results of this research could be used to evaluate the air pollution deposition models and for ecological impact estimations.     

Ion elution and release sequence from deep snowpacks in the central Sierra Nevada,California

Elution of Cl^?, SO₄ ^2?, NO₃ ^?, and H⁺ often occurred in that order at a site in the central Sierra Nevada, California, that receives an annual average of 1000 cm of snowfall which is low in acidic components. During eight winter periods of above-base level snowpack outflow, and one spring melt period, on the average 25% of the ions were discharged at the following percentages of outflow volumes: Cl^? at 11%, NO₃ ^? at 13%, SO₄ ^2? at 18%, and H⁺ at 20%. Seven of eight winter outflows were associated with low ionic strength rainfall onto the snowpack. Mean solute concentrations during the first 25% and first 50% of the total outflow were significantly greater than during the last 75% and last 50% of the total outflow for Cl^?, NO₃ ^?, and SO₄ ^2?, but not for H⁺. Maximum solute concentrations were up to 2.9 times the overall event volume-weighted mean concentrations for Cl^?, 3.7 times for NO₃ ^?, 3.0 times for SO₄ ^2?, and 2.9 times for H⁺.