Fixation of radiocaesium in an acid brown forest soil

The OAh and Ah horizons of acid brown and podzolic forest soils are reported to fix more radiocaesium than the mineral B horizons beneath them. We determined the respective influence of organic matter and clay minerals on the magnitude of Cs⁺ retention in a strongly acid brown forest soil in Belgium. The soil contained mica throughout the profile. Vermiculite was identified in the OAh and Ah horizons, and hydroxy interlayered vermiculite (HIV) in the Bw horizon. The OAh and Ah clay fraction retained much more Cs⁺ than the Bw horizon. The extraction of Al interlayers by Na-citrate resulted in a marked increase in Cs⁺ fixation in the Bw clays as well as the collapse of the vermiculitic layers after K⁺ saturation. Organic matter had a strong but indirect effect on Cs⁺ fixation. In the Bw horizon, acid weathering of layer silicates releases free Al and produces HIV minerals in which Al polymers block the access of radiocaesium onto Cs⁺-specific sites. In OAh and Ah horizons, free Al is complexed by organic acids. Consequently, the interlayer specific sites remain accessible for Cs⁺ fixation.     

Mineralogical control of organic carbon dynamics in a volcanic ash soil on La Réunion

In soil carbon dynamics, the role of physicochemical interactions between organic matter and minerals is not well understood nor quantified. This paper examines the interactions between soil organic matter and poorly crystalline aluminosilicates in a volcanic ash soil on La Réunion in the southern tropics. The soil examined is a profile composed of a surface soil (L-Ao-E-Bh) overlying four buried horizons (horizons 2Bw, 3Bw, 4Bw, 5Bw) that have all developed from successive tephra deposits. Non-destructive spectroscopy (XRD, FTIR and NMR of Si and Al) showed that the mineralogical composition varies from one buried horizon to another. Further, we show that buried horizons characterized by large amounts of crystalline minerals (feldspars, gibbsite) have the least capacity to store organic matter and the fastest carbon turnover. In contrast, buried horizons containing much poorly crystalline material (proto-imogolite and proto-imogolite allophane, denoted LP-ITM) store large amounts of organic matter which turns over very slowly. To understand the mechanism of interactions between LP-ITM and organic matter better, we focused on a horizon formed exclusively of LP-ITM. We demonstrate, using Δ¹⁴C and δ¹³C values, that even though LP-ITM is extraordinarily effective at stabilizing organic matter, C linked to LP-ITM is still in dynamic equilibrium with its environment and cycles slowly. Based on Δ¹⁴C values, we estimated the residence time of organic C as ∼ 163 000 years for the most stabilized subhorizon, a value that is comparable to that for organic carbon stabilized in Hawaiian volcanic soils. However, this calculation is likely to be biased by the presence of microcharcoal. We characterized the organo-mineral binding between organic matter and LP-ITM by ²⁷Al NMR, and found that the organic matter is not only chelated to LP-ITM, but it may also limit the polymerization of mineral phases to a stage between proto-imogolite and proto-imogolite allophane. Our results demonstrate the important role of poorly crystalline minerals in the storage of organic C, and show that mineral and organic compounds have to be studied simultaneously to understand the dynamics of organic C in the soil.     

Acidity neutralization mechanism in a forested watershed in Central Japan

The contributions of cation exchange and mineral weathering to the neutralization of acidity in the Jingahata watershed in central Japan were estimated through a laboratory weathering experiment and runoff chemistry measurements. The laboratory experiment was conducted in a stirred-flow reactor for a whole soil sample collected from the C horizon in the watershed. The concentration ratios of base cations (Ca²⁺, Mg²⁺, K⁺ and Na⁺) to Si (BC/Si) released during the steady-state stage of the laboratory experiment were in good agreement with the ratios of the net flux of base cations to the flux of Si in the streamwater (BC _{N ET}/Si _L).This result suggests that the acidity in the watershed is neutralized primarily by mineral weathering without causing a net loss of base cations from exchange sites. The alkalinity/acidity balance estimated for the watershed shows that the total weathering rate of base cations is approximately 3.26 keq ha^?1 yr^?1. Weathering of plagioclase (An₄₁) contributes 83% of the total weathering rate. The dominant acidity source is CO₂ released within the soil horizons, accounting for roughly 85% of the total acidity flux (3.20 keq ha^?1 yr^?1). This high internal production of acidity suppresses the relative importance of atmospheric acidity inputs (0.3 keq ha^?1 yr^?1).     

The seasonal variation in soil water acid neutralizing capacity in peaty podzols in Mid-Wales

Between 1985 and 1990, bulk precipitation and soil solution from the organic (Oh) and mineral (Bs) horizons of a well developed podzol were regularly sampled at a moorland catchment in Mid-Wales. Samples were analysed for pH, major cations, major anions, and dissolved organic carbon (DOC). Acid neutralizing capacity (ANC) was estimated by the charge balance method. Average monthly ANC of soil solutions from the Oh horizon varied seasonally, with a maximum in July and a minimum in February. In contrast, H⁺ concentrations varied little. Solute deposition, dominated by sodium and chloride, also varied seasonally with a winter maximum, which is reflected in the soil solution chemical composition. In the Oh horizon during winter, the increase in base cation (Na) concentrations led to release of H⁺ through ion exchange. ANC declined in the absence of any buffering mechanism. In summer, the depletion of exchangeable acidity that occurred in winter, was replenished by H⁺ produced by the dissociation of organic acids. During this period, organic anions contribute to an increase in ANC, while H⁺ concentrations remained similar to those in winter. These processes probably influenced the acidity and ANC of Bs horizon soil solutions but to a lesser extent than in the Oh horizon. Other mechanisms such as weathering and ion exchange involving H⁺ and Al may buffer solution acidity in the mineral soil.     

The effects of feeding byOniscus asellus (Isopoda) on nutrient cycling in an incubated hardwood forest soil

Summary Oniscus asellus produced changes in the nutrients leached from Oie and Oa horizons of a hardwood forest soil. Soil with isopods lost more K⁺ (54%) from the Oie horizon and more Ca²⁺ (25%), Mg²⁺ (40%), and water-extractable S (23%) from the Oa horizon than soil without isopods. In contrast, soils with isopods lost less Ca²⁺ (39076) from the Oie horizon and less dissolved C-bonded S (33%) from the Oa horizon than soil without isopods. In addition, the Oia and Oa horizons exhibited different nutrient dynamics. When isopods were present, the Oa horizon leachates accumulated more Na⁺ K⁺, Ca²⁺, Mg²⁺, NO₃ ^– , water-soluble SO₄ ^2–, and dissolved C-bonded S, and the Oie horizon retained more of these nutrients. The type of leaching solution also had a major effect on nutrients. Leaching with a simulated soil solution resulted in smaller nutrient losses for K⁺ and Mg²⁺ in both horizons and for Na⁺, Ca²⁺, and NO₃ ^– in the Oa horizon than leaching with distilled water.     

Shrinkage of initially very wet soil blocks, cores and clods from a range of European Andosol horizons

In advanced stages of volcanic ash soil formation, when more clay is formed, soil porosity values and soil water retention capacities are large and the soils show pronounced shrinkage on drying. Soil shrinkage is a key issue in volcanic soil environments because it often occurs irreversibly when topsoils dry out after changes from permanent grassland or forest to agriculture. European Andosols have developed in a wide range of climatic conditions, leading to a wide range in intensity of both weathering and organo‐mineral interactions. The question arises as to whether these differences affect their shrinkage properties. We aimed to identify common physically based shrinkage laws which could be derived from soil structure, the analysis of soil constituents, the selected sampling size and the drying procedure. We found that the final volumetric shrinkage of the initially field‐wet (56–86% of total porosity) or capillary‐wet (87–100% of total porosity) undisturbed soil samples was negatively related to initial bulk density and positively related to initial capillary porosity (volumetric soil water content of soil cores after capillary rise). These relationships were linear for the soil clods of 3–8 cm³, with final shrinkage ranging from 21.2 to 52.2%. For soil blocks of 240 cm³ and soil cores of 28.6 cm³ we found polynomial and exponential relationships, respectively, with thresholds separating shrinkage and nearly non‐shrinkage domains, and larger shrinkage values for the soil cores than for the soil blocks. For a given sample size, shrinkage was more pronounced in the most weathered and most porous Andosol horizons, rich in Al‐humus, than in the less weathered and less porous Andosol horizons, poor in Al‐humus. The Bw horizons, being more weathered and more porous, shrank more than the Ah horizons. We showed that the structural approach combining drying kinetics under vacuum, soil water analysis and mercury porosimetry is useful for relating water loss and shrinkage to soil structure and its dynamics. We also found that the more shrinkage that occurred in the Andosol horizon, the more pronounced was its irreversible mechanical change.     

Adsorption complex,pH relationships in some acid mediterranean forest soil profiles

Acid soils in some mediterranean forests were investigated for the composition of the adsorption complex and the gradients in soil pH. The effective CEC (235–838 mmol_c kg^?1) and base saturation (93–98 %) are highest in ectorganic horizons. In the mineral horizons the effective CEC (23–52 mmol_c kg^?1) and base saturation (11–40 %) are much lower. The exchange complex of mineral horizons consists for 90 (AEh) to 40 percent (Bw2) of organic matter. The effective CEC of the mineral clay fraction is low (60 mmol_c kg^?1 clay). The clear trends in soil pH within the ectorganic layer of deciduous and sclerophyllous oak forests are attributed to vertical spatial separation of nitrogen mineralization (ammonification and strongly impeded nitrification) and nutrient uptake by roots (mainly NH₄). This leads to a high effective CEC in the fermentation layer and acidification of the uppermost part of the mineral soil. In contrast to the situation in temperate forests this process is impeded in mediterranean coniferous forests, where litter decomposition is extremely slow and both proton production and consumption take place in the organic rich mineral horizon.     

生物结皮发育对风沙土盐基离子释放和矿物风化的影响

为探明生物结皮发育对风沙土盐基离子释放和矿物风化的影响,以进一步明确生物结皮的风化成土作用。以典型风沙土上发育的生物结皮为对象,通过模拟淋溶试验比较不同类型生物结皮(藻结皮、藻—藓混生结皮和藓结皮)覆盖土壤的盐基离子释放规律,探究盐基离子释放量随淋溶液pH的变化趋势,以及量化生物结皮覆盖土壤的矿物风化速率。结果表明:矿物风化反应阶段不同种类盐基离子的淋出量均较为平缓,生物结皮覆盖土壤的各盐基离子总淋出量表现为Ca²⁺＞K⁺＞Mg²⁺＞Na⁺,其中藻结皮覆盖土壤的盐基离子总淋出量最高,比无结皮、混生结皮和藓结皮分别增加了112.0%,31.2%,27.1%。淋溶液pH显著影响盐基离子的淋溶释放,且其作用程度因离子种类和结皮类型而异。生物结皮覆盖提升了土壤的易风化矿物含量、风化程度和速率,藻结皮、混生结皮和藓结皮覆盖土壤的风化速率相比无结皮分别提升了61.2%,27.1%,152.6%,并且风化速率随淋溶液pH降低而提升。综上,生物结皮能显著促进风沙土矿物风化,其对风沙土改良和修复具有积极意义。     

悬着水位对铝硅酸盐的稳定性及土壤发生的影响

The mineral stability and solute activities of soil solution extracted from selected horizons of seven studied pedons of Alfisols in Kentucky, USA, and the relationship between distribution of iron-manganese concretions and the restrictive layers were investigated. The results showed that the genesis and development of these soils and mineral weathering trends were strongly influenced by the depth of bedrock and the presence of perched water tables at lithic (limestone) interfaces due to the dissolution and buffering effect of limestone bedrock. The extractable Mg/Ca ratio as depth function and soil depth above bedrock could be used as indices of weathering and degree of soil development. Maximum iron-manganese concretion accumulation was found to occur in the horizon overlying clay horizon (>40% clay) with a sharp increase in clay content (>10%), which suggested that zones of Fe-Mn concretion accumulation in soils of the Inner Bluegrass Region appeared to be a sensitive genetic indicator of argillic horizons with restrictive permeability.     

Estimation of Mineral Weathering Rates under Field Conditions Based on Base Cation Budget and Strontium Isotope Ratios

Base cation (BC) concentrations of rain, throughfall, percolation from leaf litter, and soil solution were periodically measured in two forests: Kannondai (red pine stand on volcanic soil) and Yasato (deciduous stands on granitic soil). Calculation of a BC budget gave the rate of BC release from soils; the BCs originated from mineral weathering and cation exchange. Weathering rates under field conditions were estimated from the Sr isotope ratios (⁸⁷Sr/⁸⁶Sr) of water and soil samples. Isotope ratios decreased in the order rain > throughfall > percolation > soil solution. Clay and silt had extremely high isotope ratios; this suggests that the sandy fraction, whose isotope ratio was smaller than that of the soil solution, was the main contributor to mineral weathering. Estimated BC weathering rates (kmol_c·ha^?1y^?1) were 1.16 for Ca and 0.57 for Mg at Kannondai, and 0.82 for Ca and 0.51 for Mg at Yasato. The unexpected high weathering rate of granitic soil in Yasao was due to the wide coverage of the original parent material by volcanic ash. The contribution of cation exchange derived by subtraction was a little smaller than the weathering rates and was similar to the values estimated from a dynamic model that we developed.     

Contribution of separate solid-phase components to the formation of the cation exchange capacity in the main genetic horizons of meadow-chestnut soils

Different types of cation exchange capacity (CEC) and related chemical properties were determined in the main genetic horizons of meadow-chestnut soils in the mesodepressions at the Dzhanybek Research Station of the Institute of Forestry of the Russian Academy of Sciences. In the A horizon, the CEC is mainly due to the organic matter from the clay and coarse fractions, which provides 36% of the soil CEC, and to labile silicates and other clay minerals of the clay fraction. In the Bt horizon, the CEC is mainly provided by the labile minerals of the clay fraction and organic matter of the clay and coarse fractions. The standard soil CEC was found to be significantly higher than the sum of the exchangeable cations in the A horizon and slightly lower than the sum of the exchangeable cations in the Bt and Bca2 horizons. This difference can be related to the fact that the NH₄⁺ ion, which is selectively adsorbed by clay minerals, is used as a displacing cation during the determination of the exchangeable bases, while the Ba²⁺ ion, which is more selectively adsorbed by organic matter, is used during the determination of the standard CEC. In all the genetic horizons, the experimentally determined value of the standard CEC almost coincides with the CEC value obtained by summing the standard CECs of the different particle-size fractions with account for their contents; hence, this parameter is additive in nature.     

Dynamics of Sodium in Saline and Sodic Soils

Abstract

Soil salinization and sodication affect large areas of agricultural land in the world. Amelioration of these soils to make them suitable for agricultural production depends on understanding sodium dynamics and chemical interactions governing nutrient availability. Three locations in eastern Croatia were characterized to the 5‐m depth. The two solonetz‐solonchak soils were alkaline, whereas the solonetz soil had near‐neutral A/E horizon and alkaline deeper horizons. Electrical conductivity of the saturated extract (ECe) was greater than 4 dS m^?1 in the top horizons in the solonetz‐solonchak soils. The solonetz soil had 2.8–4.7 dS m^?1 in shallow A/E, CG, and G horizons and up to 6.3 dS m^?1 below 1.5 m. Highly alkalinized sodic horizons (exchangeable sodium percentage, ESP >20) had 24–47% Ca²⁺ and 27–33% Mg²⁺ on the cation exchange complex. Sodium adsorption ratio (SAR) was high (18–26) in the P horizon and even more so in Bt,na horizon (35–36) of solonetz‐solonchak soils. A strong negative exponential relationship existed between soluble Ca²⁺ and SAR (SAR increased greatly when Ca²⁺ dropped to around 3 mg dm^?3). An increase in pH to greater than 8.4 resulted in an exponential increase in SAR. Leaching of Na⁺ with successive volumes of water was similarly effective for the P and Bt,na horizons in the solonetz‐solonchak soils, but SAR remained greater than 15 even after six successive cycles of leaching. In conclusion, extensive amelioration of tested soils with gypsum and leaching will be required to overcome poor physical and chemical characteristics caused by various degrees of alkalization and sodication to bring these soils into production.     

A Merging Algorithm for Aerosol Size Distribution from Multiple Instruments

The work focuses on application of linear regression method for assessment of soil physicochemical parameters influence on ¹³⁷Cs accumulation. Besides organic matter content and pH, the parameters related to sorption properties of mineral parts and mobile ions concentration were considered. Before linear regression model is applied the data were transformed using Box–Cox formula. Selection of explanatory variables for regression was based on Akaike Information Criterion (AIC). Analysis of residuals distribution showed that linear regression can be applied for assessment of Cs⁺ accumulation in soil horizons. The important conclusion is that Cs⁺ cation migration in soil is usually influenced by more than a single horizon parameter. Common influence of two or more parameters on ¹³⁷Cs activity in soil horizon was observed. Our results suppose that migration of Cs in soil is affected mainly by horizon’s acidity, presence of minerals and ion exchangeable substances. Some processes are probably affected by Cs⁺ individual properties, but other ones are not so selective.     

Soil–landscape relationships at the lower reaches of a watershed at Bear Creek near Oak Ridge,Tennessee

The watersheds at Bear Creek, Oak Ridge, TN, have similar soil–landscape relationships. The lower reaches of many of these watersheds consist of headwater riparian wetlands situated between sloping non-wetland upland zones. The objectives of this study are to examine the effects of (i) slope and geomorphic processes, (ii) human impacts, and (iii) particular characteristics of soils and saprolite that may effect drainage and water movement in the wetlands and adjacent landscapes in one of these watersheds. A transect was run from west to east in a hydrological monitored area at the lower reaches of a watershed on Bear Creek. This transect extended from a steep side slope position across a floodplain, a terrace, and a shoulder slope. On the upland positions of the Nolichucky Shale, mass wasting, overland flow and soil creep currently inhibit soil formation on the steep side slope position where a Typic Dystrudept is present, while soil stability on the shoulder slope has resulted in the formation of a well-developed Typic Hapludult. In these soils, argillic horizons occur above C horizons on less sloping gradients in comparison to steeper slopes, which have Bw horizons over Cr (saprolite) material. A riparian wetland area occupies the floodplain section, where a Typic Endoaquept is characterized by poorly drained conditions that led to the development of redoximorphic features (mottling), gleying, organic matter accumulation, and minimal development of subsurface horizons. A thin colluvial deposit overlies a thick well developed Aquic Hapludalf that formed in alluvial sediments on the terrace position. The colluvial deposit from the adjacent shoulder slope is thought to result from soil creep and anthropogenic erosion caused by past cultivation practices. Runoff from the adjacent sloping landscape and groundwater from the adjacent wetland area perhaps contribute to the somewhat poorly drained conditions of this profile. Perched watertables occur in upland positions due to dense saprolite and clay plugging in the shallow zones of the saprolite. However, no redoximorphic features are observed in the soil on the side slope due to high runoff. Remnants of the underlying shale saprolite, which occur as small discolored zones resembling mottles, are also present. The soils in the study have a CEC of <10 cmol kg⁻¹, silt loam textures and Fe_d values of 0.5–4.3%. These soils are also mainly acidic and low in total carbon.     

Saturated hydraulic conductivity of soils in the Southern Piedmont of Georgia,USA: Field evaluation and relation to horizon and landscape properties

Saturated hydraulic conductivity (K_s) is one of the soil properties used most often to predict soil behavior and suitability for a variety of uses. Because of the difficulty in K_s measurement and its variability with depth and across the landscape, K_s is commonly predicted from other more easily evaluated properties including texture, clay mineralogy, bulk density, pedogenic structure and cementation. Of these, texture and pedogenic structure are most commonly used to estimate K_s, but the reliability of these estimates has not been evaluated for common soils in the Southern Piedmont of Georgia. Thus, the objectives of this study were to evaluate K_s for major horizons in soils and landscapes in the Georgia Piedmont and to relate K_s to morphological properties of these horizons. Ten sites across the region were selected, and 21 pedons arranged in three transects were described from auger holes and pits. For each pedon, K_s was measured in upper Bt horizons, at 140 cm below the surface (Bt, BC, or C horizon), and at a depth intermediate between the shallow and deep measurements (Bt, BC, or C horizon) with a constant head permeameter. The K_s of individual horizons ranged from 1 × 10^− 8 to 2 × 10^− 5 m s^− 1. At six of 10 sites evaluated, clayey upper Bt horizons had higher K_s than deeper horizons with less clay. This difference was attributed to weaker structure in the deeper BC horizons. Structural differences did not explain all variation in K_s with depth, however. Other soil and landscape properties including parent material composition, colluvium on lower slope positions, C horizon cementation, and depth of soil development also affected K_s of horizons in these soils and should be used to better estimate K_s.     

The mineralization rate of black soil carbon in the deep layers of Japanese volcanic ash soil may be easily accelerated by labile carbon supply

ABSTRACT

The stability of black soil carbon in the deep layers of Japanese volcanic ash soil (i.e., buried A horizons) is often explained by its unique chemical (molecular structure) and physical (associated with short-range-order minerals) recalcitrance. However, the stability of black soil C in buried A horizons may be changed by labile C supply for soil microbes. Here, we hypothesized that the mineralization of black soil C in buried A horizons of Japanese volcanic ash soil could be easily accelerated by a supply of labile C (i.e., a priming effect; PE). To test our hypothesis, we investigated the direction and magnitude of the PE with a buried A horizon in Japan using ¹³C-labeled glucose (2.188 atom %) in a short-term (21 days) incubation study. We also investigated the effect of mineral nitrogen (N), which could contribute to microbial activity in this incubation study. We found that a positive PE occurred by glucose supply with (182%) or without (181%) mineral N input over the 21-day incubation, and its values were very similar to the PE ratios previously reported in other deep soils. The estimated mean residence time (MRT) of black soil C considering PE was clearly accelerated by glucose supply, regardless of mineral N input, compared with the initial soil MRT. These results strongly support our hypothesis that the mineralization rate of black soil C in buried A horizons is easily accelerated by a labile C supply, and it also demonstrates important implications for the effects of global warming on buried A horizons (e.g., increased root exudation, fine root biomass supply, and N deposition) in Japanese volcanic ash soils.     

Minirhizotron quantification of soybean root growth as affected by reduced A horizon in soil

Shallow soil A horizon (topsoil) caused by soil erosion and soil movement from cultivation is known to reduce soil and crop productivity. The reduction may be related to limitation of root growth. A field study was conducted to investigate the effects of topsoil thickness on distributions of root density and growth. Soybeans [Glycine max (L.) Merr.] were grown on plots of Mexico silt loam (fine, montmorillonitic, mesic Mollic Endoaqualfs) with topsoil thicknesses of 0, 12.5, 25.0, and 37.5 cm above the Bt horizons. Root density was measured 60 and 90 days after planting using a minirhizotron video‐camera system. Root density was significantly reduced as topsoil thickness decreased from 37.5 to 0 cm. Mean density and net change of the density across profile between 30 and 60 days of growth had a linear function of topsoil thickness. The reduction and lower activity induced by shallow topsoil were attributed to detrimental properties in the Bt horizons. Root distribution pattern and rooting depth were not significantly affected by topsoil thickness. The roots appeared to be accumulated on the upper layers of the Bt horizons. Roots growing in thicker topsoil were more active than roots growing without topsoil. High soil moisture content during the growing season may mitigate the detrimental effects of shallow topsoil, inhibit root penetration, and enhance root activity.     

The acid buffer capacity of some finnish forest soils: Results of acid addition laboratory experiments

Batch acid addition experiments were carried out to determine the acid buffer capacities (amount of acid required to lower soil pH by one unit) of forest soils. Samples of O, E, B (or BC), and C horizons taken from 29 podzolic profiles in southern Finland were used in the experiments. Subsamples of soil were equilibrated for 24 h with NaCl solution containing additions of HCl acid. Cation exchange, mineral dissolution (weathering), and the protonation of organic matter all appeared to have been involved in the buffering of the acid additions. For the O horizon samples, most of the cations released in response to the acid additions were base cations. For the mineral soil samples, most of the cations released were Al³⁺ ions. With the exception of a few samples, the added acid was not fully neutralised and pH was lowered even with the lowest addition treatment. However, the acid addition treatments corresponded to many times the regional annual acid deposition load (1.6–2.0 cmol(c) m^?2). Calculated acid buffer capacities (cmol(c) kg^?1 pH^?1) ranged from 9.8 to 40.8 for O horizon soil samples and from 0.1 (C horizon) to 5.2 (E horizon) for the mineral soil samples. Total acid buffer capacities for a profile (to a depth of 50 cm) ranged from 500 to 2349, with a mean value of 1091 cmol(c) m^?2 pH^?1. It is concluded that, in addition to CEC and base saturation, acid buffer capacity is a useful measure to describe the ecological effects of acid deposition on soil.     

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.     

Analysis of Proton Generation and Consumption of Forest Surface Soils in Hokkaido, Northern Japan

We determined proton budgets of surface soils in a deciduous forest (Df) and a coniferous forest (Cf) of Volcanogenous Regosols in Tomakomai, Hokkaido of northern Japan. The total H⁺ source was 12.9 and 11.6 kmol_c ha^?1 y^?1 at Df and Cf respectively, and the external H⁺ was 1% at Df and 2% at Cf. The primary H⁺ sources were vegetation uptake of base cations and nitrification, while the major H⁺ sinks were release of base cations and NO₃ ⁺ uptake by vegetation. Leaching incubation experiments using A horizon soils including Df and Cf with NH₄ ⁺ solutions (5.3, 15.9 mg N L^?1) showed that H⁺ from nitrification was generally higher in the Df soil than Cf soil, and nitrification of Tomakomai Df soil was the highest in both treatments. Results of multiple regression analyses suggested that pH_kCl and exchangeable Ca²⁺ contributed to the H⁺ generation via nitrification. Leaching experiments with dilute HCl (pH 3.3) revealed that cation release (mainly Ca²⁺) occurred, and the proportion of release by decrease of exchangeable cations was higher than that by mineral weathering. Mineral weathering in the Tomakomai soil was higher than the other soils.