Direct contribution by soil arthropods to nutrient availability through body and faecal nutrient content

Summary The direct contribution made by soil arthropods to nutrient dynamics was investigated in pine forests that differed in soil nutrient status. Nutrient concentrations (K⁺, Ca²⁺, Mg²⁺, PO ₄ ^3– , N, C) in the most abundant species and groups of arthropods in two Pinus nigra forests were compared, and distinct differences were found among taxonomic groups. In the rank order: collembolans, oribatides, isopods, diplopods, Ca²⁺ and Mg²⁺ concentrations increased, while N and C concentrations decreased. The nutrient concentrations in individuals of the same species but originating from the different forests were similar, except for the isopod Philoscia muscorum. The total and available nutrient concentrations in food and faeces of the collembolan Tomocerus minor and the isopod Philoscia muscorum were compared. The isopod faeces contained relatively less K⁺ and Mg²⁺, and more Ca²⁺, PO ₄ ^3– , and greater N availability, compared with the food material. The collembolan faeces showed a higher availability of all nutrients measured. The N species appeared to be changed by collembolans; their faeces contained high NO ₃ ^– concentrations, while their food contained relatively high concentrations of NH ₄ ⁺ . These findings were examined in relation to their significance for ecosystem functioning. It was concluded that about 12% of the total K⁺, PO ₄ ^3– , N and 2% of the Ca²⁺ in the organic layer was found in the mesofauna. It was calculated that faeces production by the collembolans resulted in a 2.4 times higher NO ₃ ^– availability in the forest floor.     

Simulated effects of acid deposition on podzolic soils: Consequences of process and parameter aggregation

Solution cation concentrations and base cation leaching were simulated for a homogenous soil block and a soil showing five horizons of a podzolic forest soil. The dynamic model ACIDIC simulated water flow, nutrient uptake for tree growth, and cation exchange between H⁺, Al³⁺, Ca²⁺, Mg²⁺ and K⁺ in forest soil. In the multi-layer simulations exchangeable base cation concentrations changed most in the O horizon. The subsoil had a decisive effect on the pH of the runoff and base cation leaching from the soil. The one-layer model underestimated Ca and Mg leaching and overestimated H⁺ and Al concentrations in the runoff. In the eluvial and the top of illuvial horizon the solution Al / (Ca + Mg) ratio exceeded that in one-layer structure more than 10-fold. Cases with the horizon-specific cation exchange coefficient values and mean coefficient values for all layers showed only minor differences in Al / (Ca + Mg) ratio. The vertical variation in the soil chemical properties should be accounted for even if some details of processes and parameters were unavailable.     

不同白榆品系对滨海盐碱地的改良效果及盐分离子的分布与吸收

为揭示不同白榆(Ulmus pumila L.)品系对滨海盐碱地土壤盐分的改良作用及盐分离子在土壤-白榆系统中的分布与吸收特征,筛选适宜在滨海盐碱地造林的耐盐白榆品系,以中度盐渍化生境下4年生的6种白榆品系(1,5,28,30,46,105号)为试验材料,采用野外取样与室内测试相结合的方法,研究了Na+、K+、Ca2+、Mg2+等盐离子在土壤及白榆品系各器官(根、茎、叶)中的分布特征。结果表明:(1)白榆可降低滨海盐碱地土壤中盐离子及全盐含量,不同白榆品系较对照的土壤全盐含量降低了55.0%～63.1%,30号白榆降幅最大。(2)不同白榆品系将Na+、K+、Ca2+、Mg2+优先积累到叶中,且叶中维持较高的K+/Na+、Ca2+/Na+、Mg2+/Na+比值,不同白榆品系通过建立新的离子平衡以适应盐胁迫环境。(3)不同白榆品系的离子吸收选择性系数均为SK,NaSCa,NaSMg,Na,其对K+的吸收选择性大于对Ca2+、Mg2+吸收选择性;种内差异导致不同白榆品系对Na+、K+、Ca2+、Mg2+吸收选择能力不同,28号白榆根系对K+的吸收性最强,5号白榆根系对Ca2+、Mg2+的吸收性最强。     

Can acidification associated with nitrification increase available soil phosphate or reduce the rate of phosphate fixation?

Summary Using microcosms containing decomposing Pinus nigra litter, the effects of introducing two species of soil arthropods, the fungivorous collembolan Tomocerus minor and the detritivorous isopod Philoscia muscorum, have been studied. The effects of these animals on microbial respiration, on dehydrogenase and cellulase activity, and on the concentration of exchangeable macronutrients (Ca²⁺, Mg²⁺, K⁺, NO _inf3 ^sup- , NH _inf4 ^sup+ , PO _inf4 ^sup3- ) were measured. Both species enhanced microbial activity and the concentration of exchangeable nitrate, ammonium, and phosphate. Ca²⁺ and Mg²⁺ concentrations were lowered in the microcosms with animals. The differences between the two species were mainly quantitative, and it appears that the effect of isopods is direct, whereas the collembolans show direct and indirect effects. Positive effects of the presence of animals were found when microbial activities or concentrations of exchangeable nutrients in microcosms without animals were low; negative effects were found when they were relatively high. Thus, soil arthropods have a buffering role in soil processes. These results ae discussed against a background of a supposed succession of sugar fungi/bacteria to more slowly growing decomposing fungi.Dedicated to the late Prof. Dr. W. Kühnelt     

Changes in Chemical Properties of an Oxisol Due to Gypsum Application

The increasing demand for fertilizers and the fact that the world reserves of phosphorus (P) and potassium (K) are depletable make appropriate soil management a critical factor in agriculture. Techniques for the fertilizer use and soil acidity corrective are becoming increasingly necessary to minimize the cost of yield and increase the nutrient efficiency. In view of the aforementioned, the present study aimed to assess the effects of gypsum application on the leaching of cations in the soil profile. A completely randomized design in a 5 × 4 factorial arrangement, with five replicates, was used. The treatments corresponded to five gypsum rates (0, 1, 2, 4, and 8 magnesium (Mg) ha^?1) applied on broadcast of soil and at four depth sampled (0–5, 6–10, 11–15, and 16–20 cm). Gypsum application increased the fertility in depth, with the leaching of cations. There was an increase in soil pH, exchangeable K⁺ and calcium (Ca²⁺), sulfur (S–SO₄^2?), P, boron (B), and manganese (Mn) concentration, cation exchange capacity (CEC), K⁺ and Ca²⁺ saturation, Ca²⁺/Mg²⁺, Ca²⁺/K⁺, and K⁺/(Ca²⁺ + Mg²⁺) ratios, and electrical conductivity in soil depth. On the other hand, there was a decrease in exchangeable Mg²⁺ and potential acidity hydrogen and aluminum (H⁺ + Al³⁺), available silicon (Si), Mg²⁺ saturation, and Ca²⁺/K⁺ and Mg²⁺/K⁺ ratio. These results demonstrate that the gypsum application in an Oxisol with 690 g kg^?1 of clay improves the root system with a significant increase in the soil fertility in the profile.     

Aluminium release in relation to the determination of cation exchange capacity of some podzolized New Zealand soils

In upper mineral horizons, CEC by compulsive and isotopic exchange methods, using Ba²⁺ as the saturating cation, gave higher values than the effective CEC at natural soil pH, and much higher values than CEC determined with m NH₄OAc at pH 7. Cumulative Al release during leaching was considerably higher using Mg²⁺ and Ba²⁺ chlorides than K⁺ and NH₄⁺ chlorides, and gave a different shape extraction curve. Basal spacing of the dominant dioctahedral vermiculite in the soil clays contracted from 14.5Å to 10.0–10.9 Å when saturated with NH₄⁺ and K⁺, restricting release of interlayer Al. Lower horizons, containing a large proportion of Al-chlorite in the clay fraction, which did not contract with any of the cations, showed more normal exchange behaviour. On leaching, Al release was slightly greater with K⁺ and NH₄⁺, than with Mg²⁺ and Ba²⁺, chlorides. The implication of the results for CEC measurements is discussed.     

日光温室番茄缺镁与土壤盐分组成及离子活度的关系

研究了石灰性土壤日光温室不同栽培年限及番茄不同程度缺镁的土壤水溶盐分中离子组成、比例及Mg2+、Ca2+、K+离子活度等的变化及关系.结果表明:随着栽培年限的增加,温室土壤水溶盐分中Ca2+、K+、NO3-含量显著增加;水溶性盐分中阳离子以Ca2+为主,栽培5 a后NO3-成为阴离子主要成分;土壤中NO3-含量的增加是导致土壤盐分累积的主要因素.随番茄缺镁程度的加剧,土壤水溶性盐中Ca2+、K+、NO3-、全盐量及Ca2+/Mg2+、K+/Mg2+摩尔比均呈增加趋势,番茄出现缺镁的土壤含盐量达到盐渍化水平.随着土壤盐分含量增加,Ca2+、Mg2+活度均呈指数下降趋势,番茄缺镁的土壤溶液中Mg2+和Ca2+活度显著低于不缺镁土壤,(K+)/(Mg2+)、(Ca2+)/(Mg2+)活度比显著高于不缺镁土壤,(K+)/(Mg2+)活度比随缺镁程度加剧达显著差异,番茄缺镁的土壤溶液(K+)/(Mg2+)活度比大于1.盐分累积使Mg2+活度大幅降低以及K+富集对植物吸收Mg2+的拮抗作用是石灰性土壤上番茄缺镁的主要诱因.     

Sites and processes of nutrient accumulation in the subsoil through water percolation from the plow layer in a submerged paddy soil microcosm

The leaching of nutrients from the plow layer by water percolation and their accumulation in the subsoil observed in a Japanese paddy field (Katoh et al. 2004: Soil Sci. Plant Nutr., 50, 721-729) were determined semi-quantitatively in a soil column experiment. Ca²⁺, Mg²⁺, K⁺, Mn²⁺, Fe²⁺, and phosphate in percolating water from the plow layer soil column were retained in the subsoil columns that were connected to the plow layer soil column. Fe²⁺, K⁺, and phosphate accumulated in the uppermost part of the subsoil. Accumulation of Fe²⁺ in the uppermost part of the subsoil was presmnably due to the cation exchange process with concomitant desorption of Ca²⁺. In contrast, Ca²⁺ and Mg²⁺ in percolating water from the plow layer soil colmnn accumulated once in the subsoil, and translocated downwards slowly with successive water percolation. Considerable amounts of inorganic carbon (IC) and dissolved organic carbon (DOC) in percolating water from the plow layer soil column were also retained in the subsoil columns. IC did not accumulate a gaseous form.     

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.     

Apparent cation-exchange equilibria in podzolic forest soils

The Gaines–Thomas selectivity coefficient, K, was used to express the relation between the cations in solution and the cations in exchange sites in podzolic forest soils. Soil solution was obtained by centrifuging a fresh bulked soil sample. Exchangeable cations HX, AlX, CaX, MgX and KX and effective cation-exchange capacity, CEC_e, were determined with 0.1 m BaCl₂. Apparent values of K indicated a preference of Ca²⁺ over Mg²⁺ and over Al³⁺ in O, A and B horizons (log K_Al–Ca < 0 and log K_Mg–Ca < 0), whereas log K_K–Ca and log K_H–Ca exceeded zero. The horizons were similar with respect to log K_H–Ca, and the differences in log K_Mg–Ca were small. Log K_K–Ca and log K_Al–Ca increased in the horizons in the order O < A < B. Log K_Al–Ca was not significantly correlated with the fraction AlX/CEC_e. Log K_Mg–Ca was positively correlated with the fractions HX/CEC_e and AlX/CEC_e, and negatively correlated with log (CaX/MgX). The selectivity coefficient of binary cation exchange seemed to be applicable to in situ soil solutions. However, the fraction of each cation on exchange sites should be based on the CEC_e rather than on the sum of the two cations. The latter, also, seemed to be acceptable in cases of exchangeable cations with a large relative content in soil, e.g. in Al³⁺–Ca²⁺ exchange in A and B horizons, and in H⁺–Ca²⁺ exchange in O and A horizons.     

Release of sulphate-sulphur, potassium, calcium and magnesium from spent mushroom compost under field conditions

 The release of SO₄ ^2–-S, K⁺, Ca²⁺ and Mg²⁺ from soil amended with spent mushroom compost (SMC), a byproduct of mushroom production, was measured in leachate from field lysimeters for 30 weeks. Rates of application were 0 and 80 t ha^–1 moist SMC. The SMC contained 1.7% K, 6.5% Ca, 0.4% Mg and 1.2% S (of which 87% is SO₄ ^2–-S), and has a C : S ratio of 26. The break-through curves of ion leaching were polymodal indicating the preservation of soil structure in the lysimeters and its influence on leaching. SO₄ ^2–-S release from SMC was rapid (first-order exponential) and was very similar to the release from a laboratory incubation. The release of K⁺, Ca²⁺ and Mg²⁺ was described using first/zero-order models which were also used to describe their release in the laboratory. The rate and amount of Ca²⁺ release was similar in the field and laboratory, but the amount of K⁺ (and to a lesser extent Mg²⁺) release was less in the field than in the laboratory. Recoveries of SMC applied nutrients in leachate were 80% of S (263 kg ha^–1), 3% of K (14 kg ha^–1), 16% of Ca (284 kg ha^–1) and 37% of Mg (40 kg ha^–1). Little if any S was mineralised. Using SMC could provide plants with S, K, Ca and Mg but there is potential for SO₄ ^2–-S losses via leaching. Received: 7 April 1999     

Soil Solution as Affected by Plant Residues and Nitrogen Rates

Cation mobility in acidic soils with low organic‐matter contents depends not only on sorption intensity but also on the solubility of the species present in soil solution. In general, the following leaching gradient is observed: potassium (K⁺) > magnesium (Mg²⁺) > calcium (Ca²⁺) > aluminum (Al³⁺). To minimize nutrient losses and ameliorate the subsoil, soil solution must be changed, favoring higher mobility of M²⁺ (metal ions) forms. This would be theoretically possible if plant residues were kept on the soil surface. An experiment was conducted in pots containing a Distroferric Red Latosol, with soil solution extractors installed at two depths. Pearl millet, black oat, and oilseed radish residues were laid on the soil surface, and nitrogen (as ammonium nitrate) was applied at rates ranging from 0 to 150 mg kg^?1. Corn was grown for 52 days. Except for K⁺ and ammonium (NH₄ ⁺), nitrogen rates and plant residues had little effect upon the concentrations and forms of the elements in the soil solution. Presence of cover crop residues on soil surface decreased the effect of nitrogen fertilizer on Ca leaching. More than 90% of the Ca²⁺, Mg²⁺, and K⁺ were found as free ions. The Al³⁺ was almost totally complexed as Al(OH₃)⁰. Nitrogen application increased the concentrations of almost all the ions in soil solution, including Al³⁺, although there was no modification in the leaching gradient.     

Phosphorus mineralization in subarctic agricultural and forest soils

Summary Potential P and C mineralization rates were determined in a 12-week laboratory incubation study on subarctic forest and agricultural soil samples with and without N fertilizer added. There was no significant difference in net inorganic P produced between N fertilized and unfertilized soils. The forest soil surface horizons had the highest net inorganic P mineralized, 32 mg P kg^-1 soil for the Oie and 17 mg P kg^-1 soil for the Oa. In the cropped soils net inorganic P immobilization started after 4 weeks and lasted through 12 weeks of incubation. Cumulative CO₂–C evolution rates differed significantly among soils, and between fertilizer treatments, with the N-fertilized soils evolving lower rates of CO₂–C than the unfertilized soils. Soils from the surface horizons in the forest evolved the highest rates of CO₂–C (127.6 and 89.4 mg g^-1 soil for the Oie and Oa horizons, respectively) followed by the cleared uncropped soil (42.8 mg g^-1 soil C), and the cropped soils (25.4 and 29.0 mg g^-1 soil C). In vitro soil respiration rates, or potential soil organic matter decomposition rates, decreased with increasing time after clearing and in accord with the degree of disturbance. Only soils with high potential C mineralization rates and high organic P to total P ratios, mineralized P by the end of the study. Mineralizable P appeared to be associated with readily mineralizable organic C.     

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.     

Nutrient balance in Scots pine (Pinus sylvestris L.) forest. 2. Effects of plant growth and N-deposition on soil solution and leachate chemistry in a lysimeter experiment

Three years of N application to a Cambic arenosol (Typic Udorthent) in two lysimeter series, one with and one without young saplings of Pinus sylvestris L. have produced significant changes in soil solution and leachate chemistry. An application of 30 kg N/ha^*yr^?1 significantly increased NO₃ ^? leaching from the soil. This N load was also sufficient to significantly increase the mobility of the phyto-toxic elements Al³⁺ and Mn²⁺, likewise to increase leaching of the important plant nutrients Ca²⁺, Mg²⁺ and K⁺. At a N load of 90 kg N/ha^*yr^?1 significant increase in NH₄ ⁺ leaching was observed, but total leaching of NH₄ ⁺ was still very low compared to NO₃ ^? leaching. No significant treatment effects were found for SO₄ ^2?, Fe²⁺ and Cl^? in the leachate. Trees grown in the lysimeters buffered the acidifying effect of N application and increased the leachate pH by 0.2 pH units compared to lysimeters without trees.     

Influence of surface‐applied poultry manure on topsoil and subsoil acidity and salinity: A leaching column study

It has been suggested that surface applications of animal manure can ameliorate both top and subsoil acidity. For that reason, the effects of surface incorporation (0–5 cm) of a high rate of poultry manure to an acid soil on pH and exchangeable and soluble Al in the top‐ and subsoil were investigated in a leaching column study. During the experimental period of 108 d, columns received a total of 875 mm with leaching events occurring after 9, 37, 58, and 86 d. Incorporation of poultry manure into the surface 5 cm resulted in a large rise in pH measured in both 1M KCl and in soil solution. This liming effect was attributed primarily to the substantial CaCO₃ content of poultry manure. In the 15–45 cm layer, pH_KCl was not significantly different between poultry manure and control treatments but surprisingly, soil‐solution pH was substantially less in the poultry‐manure treatments. Exchangeable Al was significantly less in poultry manure than in control in all soil layers although the effect was most marked in the 0–5 cm layer. However, although concentrations and activities of monomeric Al (Al_mono), and the proportion of total Al present as Al_mono, in soil solution were lower under poultry manure than in control in the 0–5 cm layer, the reverse was, in fact, the case in lower soil horizons. This was attributed to a soluble‐salt effect, originating from the large cation content of poultry manure, displacing exchangeable Al³⁺ and H⁺ back into soil solution. Indeed, electrical conductivity and concentrations of Ca²⁺, Mg²⁺_, K⁺, and Na⁺ in soil solution were substantially higher in the poultry‐manure than in the control treatments at all soil depths. Poultry‐manure applications also resulted in substantial increases in the concentrations of Ca²⁺_, Mg²⁺_, K⁺, Na⁺, Al_mono, NH , and NO in leachates, particularly at the fourth leaching. It was concluded that although surface application of poultry manure can raise soil pH in the topsoil, increases in soluble‐salt concentrations in soil solution can greatly modify this effect in the subsoil.     

pH and solubility of aluminium in acidic forest soils: a consequence of reactions between organic acidity and aluminium alkalinity

Data from two Podzol O and E horizons, sampled in 1-cm layers at 13 points within 2 m × 2 m plots, were used to test the hypothesis that the composition of hydrogen ions (H) and aluminium (Al) adsorbed to the solid-phase soil organic matter (SOM) determines pH and Al solubility in organic-rich acidic forest soils. Organically adsorbed Al was extracted sequentially with 0.5 m CuCl₂ and organically adsorbed H was determined as the difference between total acidity titrated to pH 8.2 and Al extracted in 0.5 m CuCl₂. The quotient between fractions of SOM sites binding Al and H (N_Al/N_H) is shown to determine the variation in pH and Al solubility. It is furthermore shown that models in which pH and Al solubility are linked via a pH-dependent solubility of an Al hydroxide and in which cation exchange between Al³⁺ and Ca²⁺, rather than cation exchange between Al³⁺ and H⁺, is the main pH-buffering process cannot be used to simulate pH or Al solubility in O and E horizons. The fraction of SOM sites adsorbing Al increased by depth in the lower O and throughout the E horizon at the same magnitude as sites adsorbing H decreased. The fraction of sites binding the cations Ca²⁺ + Mg²⁺ + K⁺ + Na⁺ remained constant. It is suggested that a net reaction between Al silicates (proton acceptors) and protonated functional groups in SOM (proton donors) is the long-term chemical process determining the composition of organically adsorbed H and Al in the lower part of the O and in the E horizon of Podzols. Thus, in the long term, pH and Al solubility are determined by the interaction between organic acidity and Al alkalinity.     

Calculations of ion activities in soil solutions from humic horizons

Concentrations of the main components and activities of Ca²⁺, Na⁺, Cl^?, and NO₃^? were determined in soil solutions displaced from chernozem samples (A₁ horizon). To calculate ion activity in these solutions, it was necessary to consider formation of Ca²⁺, Mg² and Na⁺ complexes with organic anions. If 1 : 1-composition of these complexes was assumed, dependence of their stability constants on the ionic strengths was found; this allowed a 17% average error for Ca²⁺ activity and 8% for Na⁺ activity in the calculations. As followed from the computations, 68–80% of the Ca²⁺ and Mg²⁺ were included in ion pairs and complexes with 91–97% of these amounts bound with organic anions. The values for the calcite solubility product were close to those for pure saltwater systems.     

Influence of environmental factors upon the leaching of cations from undisturbed microcosms of beech and spruce litters

The leaching of nutrient cations (Na⁺, K⁺, Mg²⁺ and Ca²⁺) from undisturbed beech and spruce litters was followed in relation to the following environmental factors: nature of the organic layers, temperature, rainfall, quality of rain and stage of humus development. Among them, temperature, quality of rain and type of humus were predominant in modifying leaching rates of the nutrients. But, when the time of sampling was considered, the effects of physical, chemical and biological transformations of the humus on the leaching of cations had to be accounted for. The complexity of the interactions occurring during leaching is also exemplified.     

Acid deposition and ion leaching from a podzolic soil under hardwood forest

The contribution of atmospheric acids to cation leaching from a podzolic soil under mature maple-birch forest in central Ontario was examined during 1983. The movement of base cations was associated largely with NO₃ ^?, SO₄ ^2? and organic acid anions in surface soil horizons, with SO₄ ^2? and NO₃ ^? below the effective rooting zone, and SO₄ ^2? and HCO₃ ^? in streamflow. Mineral soil horizons could adsorb little additional SO₄ ^2? or associated cations at current soil solution SO₄ ^2? concentrations. Therefore it is concluded that the soil in situ lacks a strong affinity for SO₄ ^2?. Current annual inputs to the forest of SO₄ ^2? and NO₃ ^? in bulk precipitation (26.4 and 18.2 kg ha^?1, equivalent to 8.8 kg S and 4.1 kg N ha^?1 , respectively) contributed significantly to cation leaching from the soil. In order to maintain exchangeable cations in soil at current levels, a rate of weathering yielding 29.6, 5.0, 4.4 and 2.2 kg ha^?1 yr^?1 of Ca²⁺, Na⁺, Mg²⁺ and K⁺, respectively, would be required.