A Critical Appraisal of Field Evidence From A Regional Survey for Acid Deposition Effects On Scottish Moorland Podzols

Samples have been collected from major horizons of 34 podzol profiles distributed throughout Scotland, all developed from granite or granitic tills and under Calluna moorland. the pH in water and calcium chloride pastes, exchangeable cations and cation exchange capacity, and extractable aluminium of the soils collected have been measured, and the results studied in relation to reported atmospheric deposition of H⁺, non-marine sulphur and nitrate. for all horizons, significant positive correlations were found between soil pH and rainfall mean pH, as might be expected when the critical load of H⁺ deposition is exceeded. Acidifying pollutant deposition also apparently increased soil extractable aluminium concentrations in the B and C horizons. However, exchangeable base cation concentrations tended to increase, rather than decrease, with increasing precipitation acidity. This effect was attributed to increases in biogeochemical cycling of base cations, increases in leaching inputs of base cations from overlying A/E horizon soils, and increases in the inputs of base cations leached from upslope. the results suggest that the simple steady state mass approach to the quantification of critical loads, as often applied, may be an oversimplification.     

Sorption of tetracycline to sediments and soils: assessing the roles of pH,the presence of cadmium and properties of sediments and soils

Batch sorption experiments were conducted to evaluate the sorption behavior of tetracycline (TC, H₃L) on sediments and soils in the presence and absence of cadmium (Cd), as affected by pH and properties of sediments and soils. The results indicated stronger nonlinearity and higher capacity of TC sorption on sediments than on soils. Sorption of TC also strongly depended on environmental factors and sediment/soil properties. Lower pH facilitated TC sorption through a cation exchange mechanism, which also took place at pH values above 5.5, where TC existed as a zwitterion (H₂L⁰) or anions (HL^- and L^2-). When pH was above 7, however, ligand-promoted dissolution of TC might occur due to TC weakening the Al-O bond of aluminum oxide and the Fe-O bond of iron oxide. Natural organic matter (NOM) plays a more important role in TC sorption than cation exchange capacity (CEC) and clay contents. The presence of Cd (II) increased TC sorption on both sediments and soils, which resulted from the decrease of equilibrium solution pH caused by Cd²⁺ exchange with H⁺ ions of sediment/soil surfaces. The increase of TC sorption was also related to the formation of TC-Cd complexes, where Cd²⁺ acted as a bridge between the sediment/soil and TC.     

The Buffer Capacity of Calcareous Soils in Gansu Province of China

In this study, we added increments of acid and base to three calcareous soils from the eastern, middle and western parts of Gansu Province (China) and to three treated soils to remove calcium carbonate, organic matter and both carbonate and organic matter, respectively. the titration curves were measured and the magnitudes of buffer capacities as a function of pH were computed. It was found that the buffer capacity of calcareous soil is mainly attributed to calcium carbonate, as expected from the chemical composition of calcareous soil, while cation exchange system, silicate buffer system and organic matter play a minor role. the results clearly show that these soils of Gansu Province will not become a problem in the near future from the entrance of H⁺ into these soils.     

Aluminium in tea plantations: mobility in soils and plants, and the influence of nitrogen fertilization

The levels of extractable aluminum (Al) in soils of tea plantations, Al concentrations in tea leaves and the impact of nitrogen fertilization on these two parameters were investigated. In addition, the properties of soils from tea plantations were compared to those from soils of adjacent non-tea fields to evaluate the effect of land use conversion (from non-tea soils to tea soils). Exchangeable Al (extracted in 1 mol l⁻¹ KCl) ranged from 0.03 to 7.32 cmol_c kg⁻¹ in 94 tea fields and decreased rapidly with increasing soil pH. In comparison with non-tea soils, tea soils had a significantly lower pH and exchangeable Mg²⁺ concentration but higher organic matter contents and exchangeable K⁺ concentration. Contents of extractable Al were not different (P > 0.05) between these two soils. The concentrations of Al in mature tea leaves correlated significantly with exchangeable Al in soil samples taken at a depth of 20–40 cm and with exchangeable Al saturations in soil sampled at␣depths of 0–20 and 20–40 cm. In the pot experiment, nitrogen fertilization significantly increased extractable Al levels but decreased soil pH and the levels of exchangeable base cations. Nevertheless, the levels of Al in mature leaves and young shoots were significantly reduced by the application of large amounts of N fertilizer.     

A Comparison of the Short-Term Dynamics of Soil “Damage” Due to Enhanced Nitrogen Deposition As Ammonium Sulphate Or Nitric Acid

An experiment has been conducted to contrast the effects of enhanced oxidised and reduced nitrogen deposition upon key chemical parameters in a Calluna moorland podzol. A 40 cm deep podzol profile, derived from granite, was reconstructed in one hundred 4.2 cm diameter cores. for 20 weeks, the cores were subjected twice weekly to simulated rainfall containing either twice ambient nitrogen deposition in Aberdeen, or further enhanced nitrogen (further 2- and 6-fold increases) as nitric acid or ammonium sulphate. to quantify the dynamics of soil change in each horizon, randomly selected cores were destructively analysed every two weeks and the soils analysed. Increased nitrogen inputs, regardless of form, substantially and immediately reduced surface soil pH_water via the mobile anion or salt effect. for the higher nitrogen treatments, the pH reduction was seen throughout the profile. Longer term soil acidification was also seen in the pH_{calcium chloride} results over the 20 weeks. at a given nitrogen deposition rate, the effects of ammonium sulphate and nitric acid on soil pH_{calcium chloride} were similar. the ammonium sulphate treatments were especially effective at reducing base saturation throughout much of the profile, the direct base cation leaching being associated with substantial ammonium accumulation. the results suggest that the direct base cation leaching caused by ammonium deposition needs to be considered when assessing atmospheric pollution “damage” to heathland soils.     

酸沉降下加速土壤酸化的影响因素

酸沉降对土壤和水域的酸化影响是土壤环境化学研究前沿的热点问题之一。酸沉降的化学组成对酸性土壤的进一步酸化起着催化剂的作用。在酸雨影响下,SO42-、NO-3、有机阴离子是加速土壤酸化和盐基淋溶损失的主要阴离子,外源H+的进入会加速铝离子水解。自然因素与人为因素导致土壤酸化的实际酸化速率差异表明:HCO3-、RCOO-在土壤剖面中的淋失状况可反映自然土壤的酸化速率,而SO42-和NO-3淋溶产生的质子负荷揭示土壤受人为因素影响的酸化速率。通过计算酸沉降的主要化学成分进入土壤前后的质子负荷平衡,与酸中和容量(ANC)相结合,反映酸沉降加速土壤酸化的进程。     

Retention of 137cesium in acid sulphate soils of South Central Thailand

Adsorption and desorption of ¹³⁷Cs by acid sulphate soils from the Nakhon Nayok province, South Central Plain of Thailand located near the Ongkarak Nuclear Research Center (ONRC) were investigated using a batch equilibration technique. The influence of added limestone (12 and 18 tons ha^-1) on ¹³⁷Cs adsorption-desorption was studied. Based on Freundlich isotherms, both adsorption and desorption of ¹³⁷Cs were nonlinear. A large portion (98.26-99.97%) of added ¹³⁷Cs (3.7 × 10³-7.03 × 10⁵ Bq l^-1) was sorbed by the soils with or without added lime. The higher lime treatments, however, favoured stronger adsorption of ¹³⁷Cs as compared with soil with no lime, which was supported by higher K_ads values. The addition of lime, the cation exchange capacity and pH of the soil increased and hence favoured the stronger adsorption of ¹³⁷Cs. Acid sulphate soils with a high clay content, medium to high organic matter, high CEC, and predominant clay types consisting of a mixture of illite, kaolinite, and montmorillonite were the main soil factors contributing to the high ¹³⁷Cs adsorption capacity. Competing cations such as NH₄⁺, K⁺, Na⁺, Ca²⁺, and Mg²⁺ had little influence on ¹³⁷Cs adsorption as compared with liming, where a significant positive correlation between K_ads and soil pH was observed. The ¹³⁷Cs adsorption-desorption characteristics of the acid sulphate soils studied exhibited a very strong irreversible sorption pattern. Only a small portion (0.09-0.58%) of ¹³⁷Cs adsorbed at the highest added initial ¹³⁷Cs concentration was desorbed by four successive soil extractions. Results clearly demonstrated that Nakhon Nayok province acid sulphate soils have a high ¹³⁷Cs adsorption capacity, which limits the ¹³⁷Cs bioavailability.     

A Comparison of the Short-Term Dynamics of Soil “Damage” Due to Enhanced Nitrogen Deposition As Ammonium Sulphate Or Nitric Acid

An experiment has been conducted to contrast the effects of enhanced oxidised and reduced nitrogen deposition upon key chemical parameters in a Calluna moorland podzol. A 40 cm deep podzol profile, derived from granite, was reconstructed in one hundred 4.2 cm diameter cores. for 20 weeks, the cores were subjected twice weekly to simulated rainfall containing either twice ambient nitrogen deposition in Aberdeen, or further enhanced nitrogen (further 2- and 6-fold increases) as nitric acid or ammonium sulphate. to quantify the dynamics of soil change in each horizon, randomly selected cores were destructively analysed every two weeks and the soils analysed. Increased nitrogen inputs, regardless of form, substantially and immediately reduced surface soil pH_water via the mobile anion or salt effect. for the higher nitrogen treatments, the pH reduction was seen throughout the profile. Longer term soil acidification was also seen in the pH_{calcium chloride} results over the 20 weeks. at a given nitrogen deposition rate, the effects of ammonium sulphate and nitric acid on soil pH_{calcium chloride} were similar. the ammonium sulphate treatments were especially effective at reducing base saturation throughout much of the profile, the direct base cation leaching being associated with substantial ammonium accumulation. the results suggest that the direct base cation leaching caused by ammonium deposition needs to be considered when assessing atmospheric pollution “damage” to heathland soils.     

Modelling the effects of acid precipitation on soil leachates: A simple approach

A model is proposed to provide a simple, yet quantitatively valid perspective for the extent of soil (and lake) acidification to be expected for chemically and biologically active soils under the threat of acid precipitation. The model attempts to predict the acid (H⁺ + Al³⁺ + Fe³⁺) and base (Na⁺ + K⁺ + Mg²⁺ + Ca²⁺) cation losses from the soil, calculated from the rate and amount of acid cation retention when the rate of acid cation input is constant. It is assumed that the total amount of acidity retained by the soil is limited and qualitatively follows a Freundlich-type “absorption” isotherm. Required input information for the model includes (i) the total amounts of acid and base cations received by the soil via precipitation and weathering (minus normal leaching losses), (ii) the exchangeable base cation content and total number of cation exchange sites of the soil prior to the onset of acid precipitation.     

模拟氮沉降对土壤酸化和土壤盐基离子含量的影响

在温室内对1年生盆栽杉木幼苗进行模拟试验,以研究氮沉降对土壤酸化和土壤盐基离子含量的影响.以NH4NO3为外加氮源,设置5种处理,分别为N0(对照,0 g m-2 a-1,以N计,下同)、N1(6 g m-2 a-1)、N2(12 g m-2 a-1)、N3(24 g m-2 a-1)和N4(48 g m-2 a-1),每处理重复6次.经过18个月的处理后,对盆栽土壤进行取样分析.结果显示,随着氮沉降量的增加,土壤pH值逐渐下降,而土壤交换性酸度和交换性Al3+则不断增加.经N1、N2、N3和N4处理后,土壤交换性盐基总量分别下降6.29%、8.94%、10.07%和10.38%,土壤阳离子交换量分别下降5.07%、7.27%、8.53%和8.83%.随氮沉降量的增加,土壤NH4+-N、NO3--N含量逐渐增加.低氮处理(N1、N2)使土壤交换性K+、Ca2+、Mg2+含量增加,而高氮处理(N3、N4)则呈相反趋势.氮沉降由于增加了土壤活性氮的含量,加速了土壤酸化,从而导致了盐基离子的淋失.图3表3参41     

模拟酸雨对森林红壤中铝的溶出及不同土层酸度变化的影响

为进一步探明酸沉降对森林红壤及生态环境的影响，模拟长沙地区降水酸度及离子组成，采用浸泡试验对两种森林红壤活性铝的释出及土壤理化性质的变化进行了研究。结果表明，模拟酸雨浸泡初期，土壤活性铝的释出量随浸泡次数的增加而增加，原始土壤pH值愈低，活性铝释出愈多；强酸度、高离子浓度（AR4）模拟酸雨对土壤中活性铝的溶出量远大于基础酸雨（AR3）及弱酸、低离子浓度酸雨（AR2）和对照酸雨（AR1）。模拟酸雨酸度愈大，对土壤pH值的影响愈明显，不同土层间，以A层土壤pH值下降最明显，B、C层土壤则下降较小。模拟酸雨模拟浸泡土壤25年后，土壤阳离子交换量均有不同程度下降，有机质含量高，原土壤阳离子交换量大的土壤下降幅度也大。     

环丙沙星在亚高山草甸不同深度土壤上的吸附及其影响因素

兽用抗菌药物环丙沙星(CIP,ciprofloxacin)的大量使用引发了人们的广泛关注.文章研究了CIP在亚高山草甸土剖面土壤上的吸附动力学、吸附热力学和pH、有机质含量、阳离子交换量等因素对吸附的影响,以揭示CIP在亚高山草甸土上的吸附机制,为CIP的生态风险评价提供一定的依据.结果表明,CIP在亚高山草甸土上的吸附过程符合准二级动力学模型,并分为快吸附和慢吸附阶段,快吸附为0—6 h,慢吸附为6—48 h.CIP在供试土壤中的吸附等温线均能被Freundlich方程及线性方程很好的拟合,且|ΔH^θ|小于40 kJ·mol^-1,说明其吸附过程以物理吸附为主.其吸附等温线符合L-型,表明在CIP浓度较低时,草甸土与CIP分子间作用力较强,而浓度增大至一定程度时,溶剂分子与CIP分子间作用力占主导地位,吸附减弱.剖面土壤上CIP的吸附量随温度升高和土壤深度增加下降,这与有机质含量、阳离子交换量、黏粒含量以及pH有关.实验表明,在pH=5时,其吸附量最高.pH值在3—5时,吸附量随pH升高而升高,而在pH>5时,吸附量随pH升高而降低.表明阳离子交换为其吸附机制之一.     

施氮与凋落物去除影响下中亚热带阔叶林土壤氮素矿化潜势和硝化潜势研究

氮沉降影响土壤氮循环,而凋落物是土壤有机氮的主要来源,因此,为了探讨氮沉降和凋落物是否去除作用下,亚热带森林土壤潜在的氮素矿化与硝化作用,选择已进行8年模拟氮沉降试验的亚热带罗浮栲(Castanopsis fabri)常绿阔叶林土壤为研究对象,野外样地氮添加设置3个水平:对照(CK,0 kg·hm^?2·a^?1)、低氮(LN,75 kg·hm^?2·a^?1)、高氮(HN,150 kg·hm^?2·a^?1),两种凋落物管理方式(保留凋落物,L和去除凋落物,R),土壤采样后,通过室内间歇淋洗好气培养法,研究土壤氮素矿化潜势差异,以及不同底物条件下(铵态氮水平:N 0,100、150、200 mg·kg^?1)土壤硝化潜势的差异。结果表明:土壤氮素快速矿化主要在培养前7 d,矿化累积量(Nt)为102.81—153.71 mg·kg^?1,矿化潜势(N0)范围为193.84—289.80 mg·kg^?1,N0依次为:保留凋落物低氮(LN-L)>保留凋落物对照(CK-L)>去除凋落物低氮(LN-R)>去除凋落物对照(CK-R)>去除凋落物高氮(HN-R)>保留凋落物高氮(HN-L);两种凋落物处理方式下,LN水平土壤的Nt与N0均高于CK、HN。保留凋落物情况下,有较高的土壤硝化潜势;在无添加硝化底物(铵态氮水平为N 0 mg·kg^?1)的条件下,野外氮添加水平高的土壤硝化潜势也高;而在添加不同硝化底物(铵态氮)的条件下,土壤硝化潜势并未随硝化底物水平的增加而增加,且硝化底物水平为N 100 mg·kg^?1时硝化潜势最大。研究表明,虽然保留凋落物可以增加土壤氮矿化潜势,而氮沉降则影响氮矿化潜势。当研究土壤硝化潜势时,应当根据土壤类型等因素选择合适的硝化底物(铵态氮)添加量。     

硫氮沉降下西北荒漠煤矿区周边土壤性质的变化特点

近年来中国大部分区域大气硫、氮沉降速率趋于平稳甚至下降,但西北地区煤炭行业的快速发展使得硫、氮沉降速率加快.燃煤电厂作为酸前体物的主要排放源之一,在其周围开展硫、氮沉降效应研究,可为合理评价煤矿区大气污染物控制措施的实施效果提供数据支撑.该文以宁东能源化工基地3个燃煤电厂为采样点,研究了电厂周围土壤化学和生物学性质的变...     

Influence of sea salts on drainage water and soil chemistry of two different soil types: soil leaching experiments under laboratory conditions

The effects of sea-salt on drainage water and soil chemistry was studied using two different soil types and setting up five soil-leaching experiments under controlled laboratory conditions. The objectives of the soil-leaching experiments were to provide information of the variability of soils and their drainage water chemistry following the input of different sea-salt solutions with different times which was similar to the precipitation input experienced during the storms in fields. Analyses were presented of major ions (Na+, Ca2+, Mg2+, Cl-, NO3-, SO4(2-) and NH4+) and pH for drainage water. At the end of the experiment, CEC (cation exchange capacity), %BS (percent base saturation), exchangeable capacity of Na, Ca and Mg and pH were also analysed for soil horizon chemistry. The results showed an increase in concentration of most of the major ions in the drainage water, though some adsorption of Na, Ca and Mg had taken place; so the result being a significant decrease in soil water pH. The chemical characteristics of each soil horizons also showed significant changes with the sea-salt applications compared to initial chemical characteristics. However, comparison of data from the four different sea-salt applications under different soil type or land-use didn't indicate the additional role that different land management could play in drainage water or soil chemistry.     

Seasonal Changes in Soil Atmospheric Co2 Concentrations in Two Upland Catchments and Associated Changes in River Water Chemistry

Seasonal changes in river water chemistry and in soil atmospheric CO₂ concentrations at two depths and drainage water solute composition at two upland peaty podzol sites in north east Scotland were monitored over 12 months. the CO₂ concentrations were controlled by changes in soil temperature and moisture status. Highest CO₂ concentrations were observed in late summer 1988 when both soil temperatures and the moisture status of the soils were high. Then maximum CO₂ concentrations of 4% (v/v) were recorded for one of the sites. No significant correlations between seasonal changes in soil CO₂ concentrations and river water solute composition were observed. Nevertheless the field results and laboratory experiments indicated that in upland areas, where soils with acid surface horizons are common, soil CO₂ substantially influences river water chemistry at baseflow, increasing the pH and cation concentration of the soil water draining into the river. the results suggest that transfer of carbon as dissolved CO₂ in drainage water is a significant pathway for CO₂ transfer to the atmosphere.     

Release of mobile forms of hazardous elements from glassworks fly ash into soils

The release of hazardous elements from the wastes of high-temperature processes represents a risk to the environment. We focused on the alteration of fly ash (FA) from glassworks collected from an electrostatic filter. FA contains elevated concentrations of Zn and Ba, among other elements. Overtime, small amounts of FA have been emitted from the factory and settled into the surrounding environment (soil). In order to assess the possible risks to the environment, samples of FA were placed in small nylon bags and deposited in 11 different soil horizons (containing diverse vegetation cover such as spruce and beech and also unforested areas). Samples of the FA in bags were exposed in the soils for 1 year. Then, the bags were collected, and the exposed soils in the direct vicinity of the FA bags were sampled. The total concentrations of Zn and Ba in the FA, as well as in the soil samples (original and exposed), were determined by ICP MS. The “mobile fraction” was determined as the exchangeable (acid extractable) fraction of the modified BCR sequential extraction procedure (SEP). The SEP results indicate that Zn and Ba may pose a potential environmental risk. Their concentrations in the first, most mobile, and bioavailable fraction increased in all the exposed soils. The most significant increases were observed in the upper soil horizons (litter and A horizon). The risk to the environment was evaluated on the basis of the Risk Assessment Code.     

施用碱渣对茶园土壤酸度和茶叶品质的影响

开展田间小区试验研究了不同施用量条件下碱渣对酸化茶园土壤的酸度和茶叶品质的影响.结果表明,施用碱渣可以显著提高土壤pH、土壤交换性盐基和盐基饱和度,降低土壤交换性酸和交换性铝含量,并使土壤中钙、镁养分保持合理比例.施用碱渣提高了茶叶中茶多酚、儿茶素、咖啡碱、氨基酸和叶绿素含量,降低了茶叶中铅含量,使茶叶品质得到改善.碱渣施用量为4 500 kg·hm-2时,可将土壤pH值调节至5.51,达到最适合茶树生长的酸度条件,该条件下生产的茶叶品质也最佳,茶叶茶多酚、儿茶素、咖啡碱、氨基酸和叶绿素含量分别比对照提高22.5%、27.8%、34.9%、69.0%和52.1%,而Pb含量下降51.2%.     

The Chemistry of Throughfall, Stemflow and Soil Water Beneath Oak Woodland and Moorland Vegetation in Upland Wales

The chemistry of bulk precipitation, throughfall, stemflow and soil waters beneath an oak wood (Quercus petraea) canopy and soil waters under moorland vegetation were measured at two sites on acid brown podzolic soils near Llyn Brianne in rural mid-Wales, UK. Between March 1986 and November 1988, precipitation was 4354 mm and annual interception losses from the oak canopy averaged 13% of incident precipitation. Throughfall and stemflow were more acid and concentrations of most solutes were increased 2- to 4-fold compared with bulk precipitation. Nitrate was the only solute retained within the tree canopy. Throughfall collected beneath patches of bracken on the forest floor was less acidic but contained substantially higher concentrations of major ions than bulk precipitation and oak throughfall. the moorland soil was more acidic, contained more exchangeable calcium but less exchangeable aluminium and potassium than the woodland soil. Soil waters beneath both vegetation types were acidic (mean pH range 4.5-4.9) and dominated by sodium and chloride. with the exception of calcium, soil water solute concentrations were greater beneath oak. These differences are ascribed to larger atmospheric inputs beneath the oak canopy compared with the shorter grasses, combined with the effect of differences in nutrient dynamics and water fluxes. Variations in soil water aluminium chemistry are explained in terms of ion exchange and podzolisa-tion processes. the water quality implications of increased upland afforestation of moorland by broadleaved trees are discussed.     

The Chemistry of Throughfall,Stemflow and Soil Water Beneath Oak Woodland and Moorland Vegetation in Upland Wales

The chemistry of bulk precipitation, throughfall, stemflow and soil waters beneath an oak wood (Quercus petraea) canopy and soil waters under moorland vegetation were measured at two sites on acid brown podzolic soils near Llyn Brianne in rural mid-Wales, UK. Between March 1986 and November 1988, precipitation was 4354 mm and annual interception losses from the oak canopy averaged 13% of incident precipitation. Throughfall and stemflow were more acid and concentrations of most solutes were increased 2- to 4-fold compared with bulk precipitation. Nitrate was the only solute retained within the tree canopy. Throughfall collected beneath patches of bracken on the forest floor was less acidic but contained substantially higher concentrations of major ions than bulk precipitation and oak throughfall. the moorland soil was more acidic, contained more exchangeable calcium but less exchangeable aluminium and potassium than the woodland soil. Soil waters beneath both vegetation types were acidic (mean pH range 4.5-4.9) and dominated by sodium and chloride. with the exception of calcium, soil water solute concentrations were greater beneath oak. These differences are ascribed to larger atmospheric inputs beneath the oak canopy compared with the shorter grasses, combined with the effect of differences in nutrient dynamics and water fluxes. Variations in soil water aluminium chemistry are explained in terms of ion exchange and podzolisa-tion processes. the water quality implications of increased upland afforestation of moorland by broadleaved trees are discussed.