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.     

Changes of Some Components of Precipitation in East Germany after the Unification

A network of 15 sites of precipitation monitoring was built-up to characterize the spatial and temporal changes of pollutants over East Germany. Rain water samples were analysed and characterized regarding their acidity, conductivity, main water soluble components (Cl^-, NO₃ ^-, SO₄ ^2-, Na⁺, NH₄ ⁺, K⁺, Ca²⁺, Mg²⁺), volume and the meteorological parameters. Dependent on the changes of emission of pollutants, resulting from the reformation of industry, the decrease of stock farming, and increase of traffic (by the factor of ≈1.5) in East Germany, a drop could be observed with the sulphate and calcium concentrations in the precipitation by 20 to 50 and 30 to 70%, respectively. An increase could not be ascertained with the nitrate concentration and the acidity.     

Long Term Trend of Chemical Constituents in Tokyo Metropolitan Area in Japan

In recent years, acid rain has been a social problem all over the world. In Japan, it is also a big problem especially in the metropolitan area. Then, we have measured major ions such as H⁺, Na⁺, NH₄ ⁺, K⁺, Mg²⁺, Ca²⁺, Cl^?, NO₃ ^?, and SO₄ ^2? in precipitation and dry deposition samples which had been collected at 9 sampling sites at Hiyoshi, Mita, Kashiwa, Shiki, Fujisawa, Yokosuka, Mitaka, Hachiouji, and Ashikaga in Tokyo Metropolitan area for 10 years since 1990. The average pH of precipitation in their sites was 4.56 (n=1906). As the results of multiple regression analysis showed that pH of precipitation was determined by 5 ions such as NH₄ ⁺, nssCa²⁺(non sea salt calcium), nssCl^?(non sea salt chloride), NO₃ ^?, nssSO₄ ^2?(non sea salt sulfate) in the most of the sampling sites. Therefore, it is very important to investigate the behavior of these ions to understand the acidification of rain in Tokyo Metropolitan area. In this study, a long term trend of each ion concentration in precipitation and wet deposition was also investigated the base on the data we had observed at 7 sites for 10 years by the statistical method.     

Evaluation of the Characteristics of Acid Precipitation in Taipei,Taiwan Using Cluster Analysis

This work investigated the characteristics of acid precipitation collected in Taipei, Taiwan during 1991–1995 by performing cluster analysis. The extent to which meteorological conditions influence precipitation chemistry was also elucidated. Three potential sources of water-soluble ions in rainwater were identified: seasalt aerosols (Na⁺, Cl^- and Mg²⁺), anthropogenic pollutants (H⁺ and NO₃ ^-), and mixing sources associated with sulfate (nss-SO₄ ^2-, NH₄ ⁺ and Ca²⁺). As the northeast flow prevailed during the northeast monsoon season, the concentrations of seasalt and sulfate ions in rainwater were significantly high. During that season, a typically high ratio of nss-SO₄ ^2-/NO₃ ^- was also observed, indicating that Taipei might receive foreign pollutants via a long-range transport. In contrast, when the Pacific high dominated the region, nitrate concentration in rainwater was significantly elevated. Also during that period, the ratio of nss-SO₄ ^2-/NO₃ ^- was substantially lower, indicating the prominence of acidic substances contributed by local sources.     

Comparison of Long-Term Precipitation Chemistry Measurements at the Hubbard Brook Experimental Forest,New Hampshire

From 1978 through 1989, a wet-onlyprecipitation collector operated for the NationalAtmospheric Deposition Program, an independantwet-only collector, and a bulk precipitation collectorwere co-located at the Hubbard Brook ExperimentalForest (HBEF) in central New Hampshire. A secondbulk precipitation collector was maintained at anotherlocation within the HBEF. There were statisticallysignificant differences between the chemistry fromco-located wet-only collections for Ca²⁺,K⁺, NH₄ ⁺, pH, and NO₃ ^-. Thedifferences for K⁺ and pH though statisticallysignificant were very small but consistant. Thedifferences for Ca²⁺ were related to earlycontamination problems, and differences inNH₄ ⁺ and NO₃ ^- were related toepisotic events. Bulk precipitation was significantlyricher in K⁺ than wet-only precipitation. Therewere no differences for any ions between the bulkcollections at the two locations. While there wereminor differences, after 1981 when the contaminationproblems had been resolved, data from all collectorsat all locations adequately characterized theprecipitation chemistry of the site.     

基于地理加权回归模型的博斯腾湖湖滨绿洲土壤盐分离子含量高光谱估算

以博斯腾湖湖滨绿洲为研究区,分析HCO_3~–、Cl~–、SO_4~(2–)、Ca~(2+)、Mg~(2+)、Na~++K~+等主要土壤盐分离子含量与土壤高光谱反射率的分数阶微分光谱变换与RSI、DSI、NDSI等二维土壤指数的相关性优选特征波段,构建基于地理加权回归模型的土壤盐分离子含量估算模型。研究结果表明:Na~++K~+的微分变换特征波段集中在468～724 nm与1 182～1 539 nm,二维土壤指数的特征波段集中在1 742～2 395 nm,基于RSI的特征波段优选下地理加权回归模型对Na~++K~+含量的估算效果较好,建模集R~2=0.94,RMSE=0.22,验证集R~2=0.74,RMSE=0.19;SO_4~(2–)含量在1.2阶优选的位于469～636 nm波段估算效果较佳,建模集R~2=0.91,RMSE=0.02,验证集R~2=0.75,RMSE=0.33;Ca~(2+)、Mg~(2+)优选的特征波段主要集中在912～2 340 nm的近红外波段;Cl~–含量在1阶的近红外波段建模效果较好,建模集R~2=0.74,RMSE=0.03,验证集R~2=0.93,RMSE=0.11;含量相对较高的Na~++K~+、SO_4~(2–)、Cl~–的地理加权回归模型精度高于含量较低的Ca~(2+)、Mg~(2+)。     

Chemical Composition of Precipitation, Throughfall and Soil Solutions at Two Forested Sites in Guangzhou, South China

Rain water at two forested sites in Guangzhou (south China) show high concentrations of SO₄ ^2?, NO₃ ^? and Ca²⁺ and display a remarkable seasonal variation, with acid rain being more important during the spring and summer than during the autumn and winter. The amount of acid rain represents about 95% of total precipitation. The sources of pollutants from which acid rain developed includes both locally derived and long-middle distance transferred atmosphere pollutants. The seasonal variation in precipitation chemistry was largely related to the increasing neutralizing capacity of base cations in rainwater in winter. Soil acidification is highlighted by high H⁺ and Al³⁺ concentrations in soil solutions. The variation in elemental concentration in soil solution was related to nitrification (H⁺, NH₄ ⁺ and NO₃ ^?) and cation exchange reaction (H⁺, Al³⁺) in soil. The negative effect of soil acidification is partly dampened by substantial deposition of base cations (Ca²⁺, Mg²⁺ and K⁺) in this area.     

Evalution of Acid Deposition in Korea

This study was carried out to evaluate acid depositions and to understand their effect. Wet precipitation has been collected at twenty-four sites in Korea for one year of 1999. The ion concentrations such as H⁺, Na⁺, K⁺, Mg²⁺, NH₄ ⁺, Ca²⁺, Cl^?, NO₃ ^? and SO₄ ^2? were chemically analyzed and determined. Precipitation had wide range of pH(3.5～8.5), and volume-weighted average was 5.2. The contribution amounts of Cl^?, SO₄ ^2? and NO₃ ^? in anion were shown to be 54%, 32%, and 14%, respectively and those of Na⁺ and NH₄ ⁺ in cation were 32% and 25%. The ratios of Cl^? and Mg²⁺ to Na⁺ in precipitation were similar to those of seawater, which imply that great amount of Cl^? and Mg²⁺ in precipitation could be originated from seawater. The concentration of H⁺ is little related with SO₄ ^2?, NO₃ ^? and Cl^? ions, whereas nss^?SO₄ ^2? and NO₃ ^? are highly correlated with NH₄ ⁺, which could suggest that great amount of SO₄ ^2? and NO₃ ^? exist in the form of ammonium associated salt. The annual wet deposition amounts (g m^?2year^?1) of SO₄ ^2?, NO₃ ^?, Cl^?, H⁺, NH₄ ⁺, Na⁺, K⁺, Ca²⁺ and Mg²⁺ were estimated as 0.88～4.89, 0.49～4.37, 0.30～9.80, 0.001～0.031, 0.06～2.15, 0.27～4.27, 0.10～3.81, 0.23～1.59 and 0.03～0.63.     

Geochemical Distribution of Selected Heavy Metals in Stream Sediments Affected by Tannery Activities

Bayesian regularized back-propagation neural network (BRBPNN) was developed for trend analysis, acidity and chemical composition of precipitation in North Carolina using precipitation chemistry data in NADP. This study included two BRBPNN application problems: (i) the relationship between precipitation acidity (pH) and other ions (NH₄ ⁺, NO₃ ^?, SO₄ ^2?, Ca²⁺, Mg²⁺, K⁺, Cl^? and Na⁺) was performed by BRBPNN and the achieved optimal network structure was 8-15-1. Then the relative importance index, obtained through the sum of square weights between each input neuron and the hidden layer of BRBPNN(8-15-1), indicated that the ions' contribution to the acidity declined in the order of NH₄ ⁺ > SO₄ ^2? > NO₃ ^?; and (ii) investigations were also carried out using BRBPNN with respect to temporal variation of monthly mean NH₄ ⁺, SO₄ ^2? and NO₃ ^? concentrations and their optimal architectures for the 1990–2003 data were 4-6-1, 4-6-1 and 4-4-1, respectively. All the estimated results of the optimal BRBPNNs showed that the relationship between the acidity and other ions or that between NH₄ ⁺, SO₄ ^2?, NO₃ ^? concentrations with regard to precipitation amount and time variable was obviously nonlinear, since in contrast to multiple linear regression (MLR), BRBPNN was clearly better with less error in prediction and of higher correlation coefficients. Meanwhile, results also exhibited that BRBPNN was of automated regularization parameter selection capability and may ensure the excellent fitting and robustness. Thus, this study laid the foundation for the application of BRBPNN in the analysis of acid precipitation.     

塔里木盆地西南缘典型灌区土壤盐渍化特征分析——以塔吉克阿巴提镇为例

在野外GPS定点定位调查、土壤样品分析的基础上,借助Excel和ArcGIS9.3等软件,对新疆自治区喀什市岳普湖县塔吉克阿巴提镇0-30cm土层的盐离子特征、灌区土壤盐渍化现状及空间分布特征进行了分析。结果表明,0-30cm土层土壤中的离子以Cl^-,SO₄^2-,Na⁺,Ca²⁺为主Na+与Cl^-呈极显著正相关关系,相关系数为0.98,HCO₃^-与其它6种离子(Na⁺,Ca²⁺,Mg²⁺,K⁺,Cl^-,SO₄^2-)呈负相关关系受灌排系统影响较大的农田0-30cm土壤中Cl^-/SO₄^2-比值远小于不受灌排系统影响的荒地农田和荒地0-30cm土壤中的Cl^-/SO₄^2-比值与总盐呈正相关关系,相关系数依次为0.68和0.32。现阶段对塔吉克阿巴提镇灌区农业危害最严重的是氯化物-硫酸盐盐渍化土,硫酸盐盐渍化土表现为盐渍化土地向非盐渍化土地转变的过渡类型非盐渍化农田及轻度盐渍化农田主要分布在开垦较早,灌排系统畅通的区域,灌排系统不畅通的区域仍然处于脱盐缓慢或持续积盐的状态。     

Effect of cations on the growth of fluorescent pseudomonad isolates from spinach roots grown in soils with different salinity levels

Abstract

Effect of Inorganic ion concentrations in culture solution on the growth of Pseudomonas putida and P. fluorescens Isolates from spinach roots grown in soils with high-salinity (H-soil) and low-salinity (L-soil) levels was investigated. Both H- and L-soils were taken from the topsoil of a greenhouse for spinach cultivation and a nearby fallow field, respectively. In the H-soil inorganic ions had accumulated due to the high rates of application of fertilizer. Among the ions, the concentrations of Ca²⁺, NO₃ ^-, and SO₄ ^2- in the H-soil were significantly higher than those in the L-soil. Among the inorganic ions tested (K⁺, Na⁺, Ca²⁺, Mg²⁺, Cl^-, NO₃ ^-, and SO₄ ^2-), Ca²⁺ was found to be the most inhibitory on the growth of isolates. In addition, the isolates from the H-soil were more Ca²⁺-tolerant than those from the L-soil.

Consequents the growth tolerance to Ca²⁺ stress of the total 80 isolates, 40 each from the H-soil and L-soil, was compared at 150 mM Ca²⁺. Most isolates from the H-soil showed a significantly higher tolerance. The higher tolerance to Ca²⁺ of the isolates from the H-soil may have been acquired through selection under increasing Ca²⁺ stress in the field. The Ca²⁺ tolerance of the fluorescent pseudomonad strains may account for their survival and root-colonizing activity in soils with Ca²⁺ accumulation.     

Niederschlags-Chemismus und atmosphärische Element-Deposition in einem an der Nordseeküste von Schleswig-Holstein gelegenen Agrarökosystem

Precipitation chemistry and atmospheric element-deposition in an agroecosystem at the North-Sea Coast of Schleswig-Holstein The objective of this study was to examine the chemistry of bulk precipitation and atmospheric element inputs in an arable soil near the North Sea coast of Schleswig-Holstein, North Germany. Bulk precipitation was collected at weekly intervals from November 1989 to October 1991. Precipitation amount, pH, electrical conductivity, and concentrations of Na⁺, K⁺, NH₄⁺, Mg²⁺, Ca²⁺, Cl^?, NO₃^?, and SO₄^2? were recorded. The average volume-weighted pH was 5.5 and the average EC was 92 μS cm^?1. Sodium and Cl^? were with 64% and 76% the dominant ions (equivalent concentration) in bulk precipitation indicating the influence of the North Sea. The contribution of marine alkalinity to neutralization reactions of bulk precipitation was negligible (1%). The neutralizing substances NH₃ (63%) and Carbonate (36%) were more important. Deposition rates were in 1990 and 1991 97.0 and 51.7 kg Na⁺ ha^?1, 6.2 and 4.0 kg K⁺ ha^?1, 15.0 and 8.4 kg Mg²⁺ ha^?1, 13.2 and 10.4 kg Ca²⁺ ha^?1, 12.3 and 9.5 kg NH₄⁺-N ha^?1, 8.0 and 5.9 kg NO₃^?-N ha^?1, 168 and 83.1 kg Cl^? ha^?1 and 19.1 and 12.7 kg SO₄^2?-S ha^?1. In 1990 both more westerly winds and stronger wind-forces occurred than in 1991 and resulted in higher inputs of marine origin. Calculated on Cl^? basis 93% of Na⁺, 55% of K⁺, 74% of Mg²⁺, 24% of Ca²⁺, and 36% of SO₄^2? were of marine origin. Atmospheric input of marine origin supplied 39–72% of Mg and 21–37% of S requirement for crop production. The North Sea is an important source providing significant amounts of these elements to agricultural crops.     

recent lake acidification and recovery trends in southern quebec,canada

A total of 51 lakes in southern Quebec, Canada, were sampled between 1985 and 1993 to study changes in water chemistry following reductions in SO₂ emissions (main precursor of acid precipitation). Time series analysis of precipitation chemistry revealed significant reductions in concentrations and deposition of SO₄ ^2- from 1981 to 1992 in southern Quebec as well as reductions in concentrations and deposition of base cations (Ca²⁺, Mg²⁺), NO₃ ^- and H⁺ in the western section of the study area. Reductions in atmospheric inputs of SO₄ ^2- have resulted in decreased lakewater SO₄ ^2- concentrations in the majority of the lakes in our study, although only a small fraction (9 of 37 lakes used in the temporal analysis) have improved significantly in terms of acidity status (pH, acid neutralizing capacity – ANC). The main response of the lakes to decreased SO₄ ^2- is a decrease in base cations (Ca²⁺+Mg²⁺), which was observed in 17 of 37 lakes. Seventeen lakes also showed significant increases in dissolved organic carbon (DOC) over the period of study. The resulting increases in organic acidity as well as the decrease in base cations could both play a role in delaying the recovery of our lakes.     

Trends in the Chemistry of Acidified Bohemian Lakes from 1984 to 1995: I. Major Solutes

Temporal changes in major solute concentrations in six Czech Republic lakes were monitored during the period 1984–1995. Four chronically-acidic lakes had decreasing concentrations of strong-acid anions (C_SA = SO₄ ^2- + NO^{3 -} + Cl^-), at rates of 3.0 to 9.0 μeq L^-1 yr^-1. Decreases in SO₄ ^2-, NO₃ ^-, and Cl^- (at rates up to 5.1 μeq L^-1 yr^-1, 3.2 μeq L^-1 yr^-1, and 0.6 μeq L^-1 yr^-1, respectively) occurred. The response to the decrease in deposition of S was rapid and annual decline of SO₄ ^2- in lake water was directly proportional to SO₄ ^2- concentrations in the acidified lakes. Changes in NO₃ ^- concentrations were modified by biological consumption within the lakes. The decline in C^SA was accompanied in the four most acidic lakes by decreases in Al_T, increases in pH at rates of 0.011 to 0.016 pH yr^{- 1}, and decreases of Ca²⁺ and Mg²⁺ (but not Na⁺) in three lakes. The acid neutralizing capacity (ANC) increased significantly in all six lakes. Increases in base cation concentrations (CB = Ca²⁺ + Na⁺ + Mg²⁺ + K⁺) were the principal contributing factor to ANC increases in the two lakes with positive ANC, whereas decrease in C_SA was the major factor in ANC increases in the four chronically-acidic lakes. The continued chemical recovery of these lakes depends on the uncertain trends in N deposition, the cycling of N in the lakes and their catchments, and the magnitude of the future decrease in S deposition.     

Deposition and Leaching of Sulphate and Base Cations in a Mixed Boreal Forest in Eastern Finland

Monthly fluxes of sulphate (SO₄ ^2-) and base cations(Ca²⁺, Mg²⁺, K⁺) were studied from 1993 to 1996 as precipitation passed through forest vegetation and surfacesoil layers in an area receiving low and declining levels of atmospheric sulphate pollution. The canopy was dominated by mature Norway spruce (Picea abies Karsten) and the soilwas a podzol developed on glacial till material. The mean annual bulk deposition of SO₄ ^2- collected in the open was 136 mol_c ha^-1 and that of Ca²⁺, Mg²⁺ and K⁺ was 44, 11 and 25 mol_c ha^-1, respectively. The annual total throughfall deposition of SO₄ ^2- was 318 mol_c ha^-1 and that of Ca²⁺, Mg²⁺ and K⁺ was 151, 64 and 181 mol_cha^-1, respectively. Sulphate was the dominant anion accompanying the base cations leached from the canopy. More than half (58%) of the annual total throughfall deposition ofSO₄ ^2- was retained by the O-horizon and only 15% leached from below the B-horizon. The annual leaching of Ca²⁺, Mg²⁺ and K⁺ from below the B-horizon was14, 25 and 9% of the annual total throughfall deposition, respectively. The transport of base cations through the soil was predominantely countered by SO₄ ^2- anions.     

Deposition of nutrients and major ions by precipitation in south-central Ontario

As part of a study of the substance budgets of lakes in south-central Ontario, a network of precipitation collectors (8 bulk, 7 wet only) was operated to measure the deposition of nutrients and major ions. Results are reported for total P, total Kjeldahl N, NO ₃ ^? ?N, NH ₄ ⁺ ?N, total N, Fe, H⁺, Ca⁺⁺, Mg⁺⁺, Na⁺, K⁺, SO ₄ ⁼ and CL^? for a two year period (August 1976–July 1978). On an equivalent basis the dominant anion in both bulk and wet precipitation was SO ₄ ⁼ , with H⁺ the dominant cation. Precipitation in the study area is more acidic than that analyzed at any other location on the Canadian Shield to date. Concentrations of ions varied by 1 to 3 orders of magnitude between individual precipitation events and annual deposition varied by as much as 2-fold in the two years of study. Annual wet deposition contributed >60% of bulk deposition for all substances except total P. Seasonal trends in deposition with summer maxima were noted for most ions. For Harp Lake, a small Precambrian Lake with a lake area of 12.6% of its total drainage area, precipitation input directly to the lake surface was an important source of nutrients and major ions. This was especially the case for P, N and H⁺ because these substances were retained by the terrestrial drainage basin.     

The role of organic horizons and canopy to modify the chemistry of acidic deposition in some forest ecosystems

To clarify the mechanisms of pH buffering in forest ecosystems, field observations of pH and ionic concentrations in precipitation (R), throughfall (Tf), stemflow (Sf), and leachates from organ c horizons (Lo) were conducted for three years at three stands in Tomakomai (TK) and Teshio (TS) in Hokkaido, northern Japan. Weighted mean rates of H⁺ input as wet deposition at TK and TS were estimated in the range from 0.3 to 1.0 and 0.4–0.6 kmol_c ha^?1 y^?, respectively. While the net H⁺ flux was reduced significantly by the forest canopy, net fluxes of other ions by throughfall, especially for Na⁺, Cl^?, and SO₄ ^2?, were apparently greater than those by precipitation. The canopy modification of the H⁺ flux was more remarkable under deciduous stands than under coniferous stands, suggesting that the efficiency of conifers as the collectors of dry deposition is greater than that of deciduous ones. More than 50% of H⁺ flux due to throughfall was absorbed by the organic horizons and the weighted mean pH of Lo at TK and TS was in the range from 4.9 to 5.5 and 5.0–5.5, respectively. Results from field observation and field leaching experiments, showed that the major H⁺ sinks of the organic horizons are exchange reaction of Ca²⁺, Mg²⁺ and K⁺. Organic acids or organo-metallic complexes of lower pK(=5.0–5.5) played a significant role as counter anions in O horizons leachate in coniferous forests. Our results indicate the importance of biogeochemical modifications in the canopy and organic horizon in acid buffering mechanisms of forest ecosystems.     

天津市滨海盐碱地刺槐种植区水盐动态变化规律

[目的]通过对滨海地区盐碱土水盐动态变化规律的研究,为该地区的土壤利用以及植树造林提供科学依据。[方法]以天津大港地区刺槐林土壤为研究对象,研究不同土层的土壤水盐年份变化和盐分离子分布特征。[结果]试验地土壤全年含水量变化范围在11.9%~28.8%;含盐量变化范围在4.2%~18.4%。春(3—5月)秋(9—11月)季节土壤含水量低,含盐量高,土壤盐分含量随土层深度增加逐渐降低;夏季(6—8月),土壤含水量高,含盐量低,土壤盐分含量随土层深度的增加逐渐升高。pH值在7.37~8.39之间,土壤中K+,Na+,Ca2+,Mg2+和Cl-春季表层土壤(0—10cm)含量最高,分别为0.04,4.27,2.69,1.04和10.03g/kg。除SO2-4和HCO-3外,其他盐分离子在春季变异系数(29.99~162.98)明显大于夏秋季节(2.87~88.13)。[结论]不同土层的土壤含水量和含盐量随当地降雨量呈明显的季节性变化;试验地区土壤属于碱性土壤,随季节变化不明显;K+,Na+,Ca2+,Mg2+和Cl-与含盐量变化趋势保持一致,SO2-4和HCO-3随季节变化没有明显的规律性;春季各盐分离子在土壤中分布极为不均。     

两种不同耐盐大麦根际中离子的分布特征

选用耐盐性较强的大麦滩引５号（Ｔ）和盐敏感大麦ＣＴ１６（Ｓ），用根袋法研究了大麦极际中各种盐分离子的分布特征及动态变化。Ｔ大麦土体的ｐＨ高于Ｓ大麦，根际则相反。与非根际比较，Ｔ大麦根际土壤中除Ｋ＾＋离子亏缺外，Ｎａ＾＋，Ｃａ＾２＋，Ｍｇ＾２＋，ＳＯ４＾２－，Ｃｌ＾－及ＨＣＯ３＾－离子均富集；而Ｓ大麦根际土壤中Ｋ＾＋和Ｎａ＾＋离子亏缺，其它离子则不同程度地富集，但除ＨＣＯ３＾－离子外，亏缺或富集的程     

绿洲盐化潮土有效锌含量与盐分离子的相关性及通径分析

以张掖市甘州区和临泽县绿洲盐化潮土为研究对象,通过采集具有代表性、正常耕作种植、前茬为玉米的典型地块0~20 cm耕层土样分析化验,研究了区域土壤有效锌和盐分离子含量特征,运用通径分析方法研究了它们之间的相关性及不同盐分离子对土壤有效锌含量的影响程度。结果表明,河西绿洲灌区盐化潮土有效锌含量介于0.289~0.736 mg/kg之间,平均为0.473 mg/kg,变异系数为18.68%,超过70%的土壤低于缺锌临界值(0.5 mg/kg),且土壤有效锌含量有随含盐量升高而降低的趋势。土壤有效锌含量与HCO_3~–、Mg~(2+)、Na~+含量之间呈极显著负相关,与Cl~–、Ca~(2+)、K~+含量之间呈显著负相关,与SO_4~(2–)含量之间的相关性不显著。Mg~(2+)对土壤有效锌含量表现出强烈的直接和间接负效应,HCO_3~–表现出很大的直接负效应和强烈的间接正效应,Cl~–、K~+和Na~+均表现出较强的直接和间接负效应,SO_4~(2–)表现出较弱的直接和间接正效应,Ca~(2+)表现出较弱的直接和间接负效应。Mg~(2+)、HCO_3~–和Na~+是影响土壤有效锌含量变化的3个主导因素,对决定系数R~2的贡献超过了68%。