施用碱稳定污泥污水土壤经γ-辐照后土壤溶液中Cu和Zn

Soil samples collected from several acid soils in Guangdong, Fujian, Zhejiang and Anhui provinces of the southern China were employed to characterize the chemical species of aluminumions in the soils. The proportion of monomeric inorganic Al to total Al in soil solution was in the range of 19% to 70%, that of monomeric organic Al (Al-OM) to total Al ranged from 7.7% to 69%, and that of the acid-soluble Al to total Al was generally smaller and was lower than 20% in most of the acid soils studied. The Al-OM concentration in soil solution was positively correlated with the content of dissolved organic carbon (DOC) and also affected by the concentration of Al³⁺. The complexes of aluminum with fluoride (Al-F) were the predominant forms of inorganic Al, and the proportion of Al-F complexes to total inorganic Al increased with pH. Under strongly acid condition, Al³⁺ was also a major form of inorganic Al, and the proportion of Al³⁺ to total inorganic Al decreased with increasing pH. The proportions of Al-OH and Al-SO₄ complexes to total inorganic Al were small and were not larger than 10% in the most acid soils. The concentration of inorganic Al in solution depended largely on pH and the concentration of total F in soil solution. The concentrat ions of Al-OM, Al³⁺, Al-F and Al-OH complexes in topsoil were higher than those in subsoil and decreased with the increase in soil depth. The chemical species of aluminumions were influenced by pH. The concentrations of Al-OM, Al³⁺, Al-F complexes and Al-OH complexes decreased with the increase in pH.     

上海市土壤中持久性毒害污染物和盐分含量特征研究

Some farmland soils in Shanghai had high salinity levels, suggesting secondary salinization of the soils. The soil problems in Shanghai were studied, including the salinity and nitrate nitrogen (NO₃^--N) concentrations, heavy metal pollution characteristics, and organochlorine pesticide (OCP) residual levels and polycyclic aromatic hydrocarbon (PAH) contents. Accumulation of NO₃^--N in vegetable soils was the most significant among different functional soils. Heavy metal pollution was significant in the samples collected from the sewage-irrigated land and roadside. The identification of the metal sources through multivariate statistical analysis indicated that Pb, Zn, Cu and Cr in urban soils were from the traffic pollutants; excessive application of fertilizer and irrigation were the main reasons for the metal pollution in agricultural soils; Ni in the observed soils was controlled by parent soils. OCPs could still be detected in farmland soils but degraded greatly in last 20 years after prohibition of their usage. PAHs with 2-3 rings were the main components in industrial soils. The concentrated PAHs in the investigated soils were likely from petroleum and coal combustion.     

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).     

Impact of drilling waste pollution on land cover in a high subarctic forest-tundra zone

Global climate changes can lead to the destruction of the permafrost zone and contribute to the active transfer of pollutants to natural waters. This can be especially pronounced in the areas of oil and gas production in the Arctic. This study aimed to define the landscape components (i.e., groundwater, soil water, soil, and indicator plant species) of chemical pollution with metals, oil hydrocarbons, and polycyclic aromatic hydrocarbons, from the discharge of drill cuttings. Studies at two sites in the forest-tundra zone of Western Siberia (Russia) were carried out within two years of pollution. Pollutant migration was found in peaty-gley heavy loamy soils and iron-illuvial clayey podburs, but lateral migration of different pollutants did not exceed 200 m. Additionally, radial migration was practically absent owing to the high buffering capacity of the soil organic horizon and the upward flow of matter in the seasonal melt layer. The main indicators of drilling waste pollution were high concentrations of Sr, Ba, petroleum hydrocarbons, and Cl^- ions. At the waste disposal sites, the concentration of Ba and Sr in the soil water were 1 150 and 1 410 μg L^-1, respectively; in groundwater, they reached 721 and 2 360 μg L^-1, respectively. In the soil, Ba and Sr accumulated in the peaty horizon (798 and 706 mg kg^-1, respectively). The concentration of Cl^- ions in the soil water at the site of waste discharge was 1 912 mg L^-1, and at a distance of 200 m, it decreased to 77.4 mg L^-1. The Cl^- concentration in the groundwater was lower, and at a distance of 200 m, it was 38.9 mg L^-1. The highest concentration of petroleum hydrocarbons in the surface layer was found in the peaty-gley soils (up to 2 400 mg kg^-1). In glandular-illuvial podburs, it was 420 mg kg^-1. In horizons BH and BC, it was close to the background values (27 and 33 mg kg^-1, respectively). Alkalinization of soils and water under the influence of drill cuttings led to the death of oligotrophic and acidophilic vegetation at a distance of up to 50 m, and to the restructuring of the species and spatial structure of plant communities up to 100 m.     

碱稳定污泥污水对土壤可提取有机碳和铜的影响

An incubation experiment was conducted to evaluate the potential for water contamination with sludge-derived organic substances and copper following land application of alkaline-stabilised sewage sludge. Two contrasting sludge-amended soils were studied. Both soils were previously treated with urban and ruralalkaline biosolids separately at sludge application rates of 0, 30 and 120 t ha^-1 fresh product. The air-driedsoil/sludge mixtures were wetted with distilled water, maintained at 40 % of water-holding capacity and equilibrated for three weeks at 4 ℃ before extraction. Subsamples were extracted with either distilled wateror 0.5 mol L^-1 K₂SO₄ solution. The concentrations of organic C in the aqueous and chemical extracts were determined directly with a total organic carbon (TOC) analyser. The concentrations of Cu in the twoextracts were also determined by atomic absorption spectrophotometry The relationship between the two extractable organic C fractions was examined, together with that between extractable organic C concentration and extractable Cu concentration. Application of alkaline biosolids increased the concentrations of soil mobile organic substances and Cu. The results are discussed in terms of a possible increase in the potential for leaching of sludge-derived organics and Cu in the sludge-amended soils.     

碱茅根际土壤盐分动态变化研究

A glasshouse experiment using a rhizobox technique was conducted to examine salt dynamics in the rhizosphere of a salt-tolerant grass, Puccinellia ciliata Bor. ‘Irwin Hunter', grown in a loamy soil, and to study the effect of rainfall flush on salt accumulation in the rhizosphere. The rhizobox (10 × 5.5 × 50 cm) had a nylon mesh (1 μm) positioned vertically in the middle to create two compartments filled with soil amended with 1 g NaCl kg^-1. The plants were grown in one compartment only. Flushed treatments received 275 mL of deionized water two days before harvest. In the plant-growing compartment, soils were sectioned vertically at 5 cm intervals. Significant differences in soil electrical conductivity (EC) (P < 0.05) and pH (P < 0.05) were observed for depths, but not between flushed and non-flushed treatments. In the no-plant compartment (rhizosphere), soil cores were taken horizontally at depths of 5, 20 and 40 cm and sliced at 1, 2, 3, 4, 5, 7, 10, 15 and 20 mm away from the roots. Soil EC and Cl^- concentration at the 5 and 20 cm depths, and Na⁺ concentration at the 5 cm depth significantly decreased (P < 0.05) with the distance away from the root, but no significant differences were observed in soil pH and concentrations of the K⁺ and Ca²⁺. The flush treatment only had significant influence on soil EC, pH, and Cl^- concentration at the 20 cm depth. Thus, salt accumulation could occur in the rhizosphere of salt-tolerant species on saline soils, and the periodic low rainfall might not have a strong influence on salt distribution in the rhizosphere and/or root zone.     

玉米秸秆应用和腐化对钙质苏打土改良的影响: 实验室试验研究

A laboratory lysimeter experiment was conducted to investigate the effects of forage corn (Zea mays L.) stalk application on the CO₂ concentration in soil air and calcareous sodic soil reclamation. The experimental treatments tested were soil exchangeable sodium percentage (ESP) levels of 1, 11, and 19, added corn stalk contents of 0 to 36 g kg^-1, and incubation durations of 30 and 60 days. The experimental results indicated that corn stalk application and incubation significantly increased CO₂ partial pressure in soil profile and lowered pH value in soil solution, subsequently increased native CaCO₃ mineral dissolution and electrolyte concentration of soil solution, and finally significantly contributed to reduction on soil sodicity level. The reclamation effciency of calcareous sodic soils increased with the added corn stalk. When corn stalks were added at the rates of 22 and 34 g kg^-1 into the soil with initial ESP of 19, its ESP value was decreased by 56% and 78%, respectively, after incubation of 60 days and the leaching of 6.5 pore volumes (about 48 L of percolation water) with distilled water. Therefore, crop stalk application and incubation could be used as a choice to reclaim moderate calcareous sodic soils or as a supplement of phytoremediation to improve reclamation effciency.     

灌溉施用氮肥后氮素在土壤中的转化及淋失状况: 土柱模拟研究

A soil column method was used to compare the effect of drip fertigation (the application of fertilizer through drip irrigation systems, DFI) on the leaching loss and transformation of urea-N in soil with that of surface fertilization combined with flood irrigation (SFI), and to study the leaching loss and transformation of three kinds of nitrogen fertilizers (nitrate fertilizer, ammonium fertilizer, and urea fertilizer) in two contrasting soils after the fertigation. In comparison to SFI, DFI decreased leaching loss of urea-N from the soil and increased the mineral N (NH₄⁺-N + NO₃^--N) in the soil. The N leached from a clay loam soil ranged from 5.7% to 9.6% of the total N added as fertilizer, whereas for a sandy loam soil they ranged between 16.2% and 30.4%. Leaching losses of mineral N were higher when nitrate fertilizer was used compared to urea or ammonium fertilizer. Compared to the control (without urea addition), on the first day when soils were fertigated with urea, there were increases in NH₄⁺-N in the soils. This confirmed the rapid hydrolysis of urea in soil during fertigation. NH₄⁺-N in soils reached a peak about 5 days after fertigation, and due to nitrification it began to decrease at day 10. After applying NH₄⁺-N fertilizer and urea and during the incubation period, the mineral nitrogen in the soil decreased. This may be related to the occurrence of NH₄⁺-N fixation or volatilization in the soil during the fertigation process.     

苏南地区土壤重金属向蔬菜的迁移研究

Vegetable fields in peri-urban areas receive large amounts of extraneous heavy metals because of rapid urbanization and industrialization in China. The concentrations of Cu, Zn, and Pb in 30 soil samples and 32 vegetable samples, collected from 30 different sites in southern Jiangsu Province of China, were measured and their transfer from soil to vegetable was determined. The results showed that the soil samples had wide ranges of pH (4.25-7.85) and electrical conductivity (EC) (0.24-3.42 dS m^-1). Among the soil samples, there were four soil samples containing higher Cu and two soil samples containing higher Zn concentrations than those specified in the Chinese Soil Environmental Quality Standard II. However, no vegetable sample was found to contain a high level of Cu or Zn. In contrast, one vegetable sample contained 0.243 mg Pb kg^-1 FW, which was above the Chinese Food Hygiene Standard, whereas the corresponding soil Pb concentration was lower than the Chinese Soil Environmental Quality Standard II. The transfer coefficients of Cu of all vegetable samples exceeded the suggested coefficient range, implying that extraneous Cu had high mobility and bioavailability to vegetables. There was no significant correlation between extractable soil heavy metal concentrations with four kinds of extractants and soil pH, EC, heavy metal concentrations in vegetables and soils, except that soil pH correlated well with the extractable soil Cu, Zn, and Pb concentrations with 1.0 mol L^-1 NH₄NO₃. Moreover, diethylenetriamine pentaacetic acid (DTPA) extraction method was a more effcient method of extracting heavy metals from the soils independent of soil pH and EC than other three methods used.     

氟化物对酸性土壤溶液组成的影响

Atmospheric emissions of fluoride from an aluminium smelter-alumina refinery located on the northern coast of Galicia, NW Spain, increase the content of fluorine in soils and vegetation in the vicinity of the complex. The effects of the addition of fluoride solutions on the chemical properties of soil samples from the area surrounding the complex were investigated in laboratory experiments. Addition of fluoride to soils resulted in increases in pH and concentrations of Fe, Al, and organic matter in the equilibrium solutions and decreases in concentrations of Ca, Mg, and K. No consistent effects were observed on the Cu, Mn, or Zn concentrations. Most of the Al in solution was bound to organic matter. Within the fraction “labile aluminium,” the concentration of Al-OH complexes decreased and the Al-F complexes increased, especially AlF3 and AlF4-, which are less toxic than Al3+ and Al-OH species.     

Effects of H2SO4 and HNO3 on Soil Acidification and Aluminum Speciation in Variable and Constant Charge Soils

The difference in effect on acidification and species of aluminum speciation between HNO₃ and H₂SO₄for two contrasting types of soils in surface charge was investigated. The results show that the effect of H₂SO₄ on acidification of variable charge soils (Ferric Acrisol and Haplic Acrisol) of subtropical regions wasweaker than that of HNO₃, due to the specific adsorption of SO₄ ^2- and the accompanied release of OH^-. For two constant charge soils, Haplic Luvisol andEutric Cambisol, the difference in effect between the two acids is small. The concentrations of total inorganic monomeric aluminum, Al³⁺, Al-F complexes and Al-SO₄complexes in the extract from variable charge soils are alsolower in H₂SO₄ systems than those in HNO₃ systems, whereas the reverse is true for constant charge soils, except the concentration of Al³⁺. For variable charge soils, Al-F complexes are the major species of inorganic monomeric aluminum at high pH butAl³⁺ might contribute to a largepart at low pH, while for constant charge soils Al-F complexes contribute almost exclusively to the inorganic monomeric aluminum. The presence of a large amount of SO₄ ^2- in the extract from the constant charge soilsleads to a higher proportion of Al-SO₄ complexes in totalinorganic monomeric aluminum than that from variable charge soil, although the numerical value of proportion is small.     

pH对酸性土壤中铝的溶出和铝离子形态分布的影响

ＰＨ对酸性土壤中铝的溶出和土壤溶液中铝离子形态分布的影响的研究结果表明,土壤中铝的溶出量随ＰＨ降低而增加,ＰＨ对不同土壤中铝的溶出的影响不同,三种土壤中铝的溶出量受ＰＨ影响的大小顺序是：红壤〉赤红壤〉砖红壤,说明不同类型土壤中铝的溶出对外来酸的敏感和程度不同。     

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     

Changes in aluminum pools of andisols due to soil acidification

Abstract

Aluminum concentrations in soil solutions are not only controlled by inorganic clay minerals but also by organically bound aluminum. The objective of this study was to determine which pools contribute to Al dissolution. Soil samples were taken at various distances from tree trunks and at various depths at the Rolling Land Laboratory (RLL), Hachioji, Tokyo. Selective dissolution techniques were used to analyze the changes in pools of solid-phase aluminum. Soil pH values around Hinoki cypresses were in the aluminum buffer range. Exchangeable aluminum contents in soils under Hinoki cypresses were 104 mmol_c kg-^?1 on the average. This value was similar to that of the cation exchange capacity (CEC) of Andisols at RLL at a soil pH of 4. The relationship between the soil pH and exchangeable, organically bound, and amorphous aluminum pools showed that dissolved aluminum ions in the soil solution were primarily derived from the amorphous Al pool. Dissolved aluminum ions were substituted with base cations of soils, resulting in the increase of the content of exchangeable Al and/or the formation of complexes with organic matter which increased the proportion of organically bound Al pools. Increase in the proportion of organically bound Al pools indicated the importance of complexation with soil organic matter for controlling the aluminum concentration in the soil solution.     

ALUMINUM SPECIATION OF AMENDED ACID TROPICAL SOIL AND ITS EFFECTS ON PLANT ROOT GROWTH

Exchangeable and soluble soil aluminum (Al) is limiting plant growth in many soils worldwide. This study evaluated the effects of increasing rates of dolomite and magnesium carbonate (MgCO₃) on Al³⁺, pH, dissolved organic carbon, cations, anions, and Al speciation on oil palm Deli dura × AVROS pisifera root growth. Dolomite and MgCO₃ additions significantly raised linearly soil solution pH, magnesium (Mg²⁺), nitrate (NO₃ ^?) and chlorine (Cl^?) concentrations; exponentially decreased the activity of phytotoxic Al species [aluminum (Al³⁺), aluminum sulfate (Al₂SO₄), and aluminum fluoride (AlF₃)]; and reduced manganese (Mn) concentration and activity. High activity of those species exponentially reduced root dry weight. Optimum oil palm growth was achieved at: <50 μM monomeric Al, < 30 μM Mn, and <0.20 unit of the ratio Al+Mn to calcium (Ca)+Mg. High activity of Al species and Mn in acidic soil solution cause significant reduction of the root growth. Soil acidity alleviation either with dolomite or MgCO₃ mitigates the toxic effect of Al and Mn.     

Aluminum solubility of strongly acidified allophanic Andosols from Kagoshima Prefecture,southern Japan

Abstract

The aluminum solubility of acidified soils both from furrows and under tree canopies of a tea garden was studied using equilibrium experiments in 0.01 mol L^?1 CaCl₂ solution systems. The soils were originally classified as allophanic Andosols. The furrow soils were more severely acidified because of the heavy application of nitrogen fertilizer, especially in the upper soil horizons (pH[H₂O] of 3.6–3.8 in the A1 and 2A2 horizons). These acidified soils were characterized by the dissolution of allophanic materials (allophane, imogolite and allophane-like materials) and by an increase in Al–humus complexes. Ion activity product (IAP) values of the strongly acidified soil horizons were largely undersaturated with respect to imogolite (allophanic clay) or gibbsite. Plots of p(Al³⁺) as a function of pH strongly indicated that Al solubility of the soils was largely controlled by Al–humus complexes, especially in the A1 horizon. In the canopy soils, which were more weakly acidified (pH[H₂O] 4.9–5.0), Al solubility was close to that of gibbsite and allophanic materials, indicating that the solubility is partly controlled by these minerals.     

单宁酸对不同pH茶园土壤中活性铝形态分布的影响

采集云南省普洱市和江西省南昌县两地典型的茶园土壤,通过添加HCl和Ca(OH)2调节土壤pH,研究不同pH(3.0、3.5、4.0、4.5)茶园土壤添加0.4 mmol·kg 1、2.0 mmol·kg 1、4.0 mmol·kg 1、8.0 mmol·kg 1、12.0 mmol·kg 1单宁酸后,活性铝形态交换态铝(Al3+)、单聚体羟基铝[Al(OH)2+、Al(OH)+2]、酸溶无机铝[Al(OH)03]和腐殖酸铝[Al-HA]的分布特征。结果表明:单宁酸添加量为0~0.4 mmol·kg 1和0~2.0 mmol·kg 1时,江西南昌和云南普洱茶园土壤中交换态铝随土壤pH的增加呈明显下降趋势,而羟基态铝、酸溶无机铝和腐殖酸铝呈逐渐上升趋势;当单宁酸浓度增至2.0 mmol·kg 1以上时,随土壤pH的增加,单宁酸对活性铝释放的抑制作用增强,各形态活性铝含量都较低,且不同pH处理土壤间的差异不显著。0~20 cm土层土壤与20~40 cm土层土壤变化规律大致相似,总体上看,下层土壤活性铝总量高于上层。云南普洱茶园土壤活性铝总量明显高于江西南昌的茶园土壤。相关分析表明,0~20 cm土层土壤中,pH与羟基态铝、腐殖酸铝、土壤酸碱缓冲容量(pHBC)呈正相关(r=0.796,P0.01;r=0.960,P0.01;r=0.852,P0.01);pHBC与交换态铝、羟基态铝呈负相关(r=0.904,P0.01;r=0.645,P0.05),而与腐殖酸铝呈正相关(r=0.795,P0.01)。同时,单宁酸加入浓度为0~0.4 mmol·kg 1时,土壤pH明显上升,之后随着单宁酸加入浓度的增加土壤pH持续下降,土壤pH(YpH)与单宁浓度(CDN)在此阶段基本符合方程:YpH=0.04CDN+3.82(R2=0.95,P0.01)的线性变化趋势,在单宁酸浓度达到8.0~12.0 mmol·kg 1时,土壤pH基本不再变化。     

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。     

Biogeochemistry of aluminum in a forest catchment in the Czech Republic impacted by atmospheric inputs of strong acids

The Lysina catchment in the Czech Republic was studied to investigate the biogeochemical response of Al to high loadings of acidic deposition. The catchment supports Norway spruce plantations and is underlain by granite and podzolic soil. Atmospheric deposition to the site was characterized by high H⁺ and SO₄ ^2– fluxes in throughfall. The volume-weighted average concentration of total Al (Al_t) was 28 mol L^–1 in the O horizon soil solution. About 50% of Al_t in the O horizon was in the form of potentially-toxic inorganic monomeric Al (Al_i). In the E horizon, Al_t increased to 71 mol L^–1, and Al_i comprised 80% of Al_t. The concentration of Al_t (120 mol L^–1) and the fraction of Al_i (85%) increased in the lower mineral soil due to increases in Al_i and decreases in organic monomeric Al (Al_o). Shallow ground water was less acidic and had lower Al_t concentration (29 mol L^–1). The volume-weighted average concentration of Al_t was extremely high in stream water (60 mol L^–1) with Al_i accounting for about 60% of Al_t. The major species of Al_i in stream water were fluorocomplexes (Al-F) and aquo Al³⁺. Soil solutions in the root zone were undersaturated with respect to all Al-bearing mineral phases. However, stream water exhibited Al_i concentrations close to solubility with jurbanite. Acidic waters and elevated Al concentrations reflected the limited supply of basic cations on the soil exchange complex and slow weathering, which was unable to neutralize atmospheric inputs of strong acids.