Impact of organic matter addition on pH change of paddy soils

Purpose

The objective of the present study was to explore the effect of initial pH on the decomposition rate of plant residues and the effect of residue type on soil pH change in three different paddy soils.

Materials and methods

Two variable charge paddy soils (Psammaquent soil and Plinthudult soil) and one constant charge paddy soil (Paleudalfs soil) were used to be incubated at 45 % of field capacity for 105 days at 25 °C in the dark after three plant residues (Chinese milk vetch, wheat straw, and rice straw) were separately added at a level of 12 g?kg^?1 soil. Soil pH, CO₂ escaped, DOC, DON, MBC, MBN, NH ₄ ⁺ , and NO ₃ ^? during the incubation period were dynamically determined.

Results and discussion

Addition of the residues increased soil pH by 0.1–0.8 U, and pH reached a maximum in the Psammaquent and Plinthudult soils with low initial pH at day 105 but at day 3 in the Paleudalfs soil with high initial pH. Incorporation of Chinese milk vetch which had higher concentration of alkalinity (excess cations) and nitrogen increased soil pH more as compared with incorporation of rice and wheat straws. Microbial activity was the highest in Chinese milk vetch treatment, which resulted in the highest increase of soil pH as compared with addition of rice and wheat straws. However, nitrification seemed to be inhibited in the variable charge soils of Psammaquent and Plinthudult but not in the constant charge soil of Paleudalfs.

Conclusions

The effectiveness of increasing soil pH after incorporation of the plant materials would be longer in low initial pH soils of Psammaquent and Plinthudult than in high initial pH soil of Paleudalfs. In order to achieve the same degree of pH improvement, higher amounts of plant residues should be applied in constant charge soils than in variable charge soils.     

pH change, carbon and nitrogen mineralization in paddy soils as affected by Chinese milk vetch addition and soil water regime

Purpose

The aim of the research was to explore the effect of Chinese milk vetch (CM vetch) addition and different water management practices on soil pH change, C and N mineralization in acid paddy soils.

Materials and methods

Psammaquent and Plinthudult paddy soils amended with Chinese milk vetch at a rate of 12 g?kg^?1 soil were incubated at 25 °C under three different water treatments (45 % field capacity, CW; alternating 1-week wetting and 2-week drying cycles, drying rewetting (DRW) and waterlogging (WL). Soil pH, dissolved organic carbon, dissolved organic nitrogen (DON), CO₂ escaped, microbial biomass carbon, ammonium (NH₄ ⁺) and nitrate (NO₃ ^?) during the incubation period were dynamically determined.

Results and discussion

The addition of CM vetch increased soil microbial biomass concentrations in all treatments. The CM vetch addition also enhanced dissolved organic N concentrations in all treatments. The NO₃–N concentrations were lower than NH₄–N concentrations in DRW and WL. The pH increase after CM vetch addition was 0.2 units greater during WL than DRW, and greater in the low pH Plinthudult (4.59) than higher pH Paleudalfs (6.11) soil. Nitrogen mineralization was higher in the DRW than WL treatment, and frequent DRW cycles favored N mineralization in the Plinthudult soil.

Conclusions

The addition of CM vetch increased soil pH, both under waterlogging and alternating wet–dry conditions. Waterlogging decreased C mineralization in both soils amended with CM vetch. Nitrogen mineralization increased in the soils subjected to DRW, which was associated with the higher DON concentrations in DRW than in WL in the acid soil. Frequent drying–wetting cycles increase N mineralization in acid paddy soils.     

Impacts of fertilization practices on pH and the pH buffering capacity of calcareous soil

Modern intensive agricultural practices, particularly the use of nitrogen fertilizers, have accelerated soil acidification on a global scale. The soil pH buffering capacity (pHBC) is often used to quantify the soil acidification rate. Calcareous soils have relatively higher pH and pHBC, reflecting the presence of carbonate minerals; however, the impact of long-term fertilization treatment on pH and pHBC is poorly understood for calcareous soils. Here, calcareous soil samples (0–20 cm) were collected from fields receiving six different fertilization treatments for 22 years: control (CK, unfertilized but planted); nitrogen (N); nitrogen and phosphorus (NP); nitrogen, phosphorus and potassium (NPK); combined manure and NPK (NPKM); and combined corn-stover and NPK (NPKS). Both pH and pHBC significantly decreased for all treatments relative to CK. NPKS treatment had the lowest soil pH. Compared with CK, the soil pHBC decreased 5.7 to 17.3% under different treatments. The calcium carbonate (CaCO₃) content was significantly reduced by fertilization treatments, with a maximum decrease under the NPKS treatment. Structural equation model (SEM) analysis revealed that calcium carbonate and soil organic matter (SOM) made important contributions to effective cation exchangeable capacity (ECEC). Soil pHBC was directly controlled by ECEC, while CaCO₃ and SOM indirectly contributed to the pHBC through ECEC. These results indicated that NPKS treatment induces more severe soil acidification, reflecting the higher H⁺ input and lower pHBC under this treatment.     

Influence of Different Forms of Iron and Aluminum on the Nature of Soil Acidity of Some Inceptisols,Alfisols, and Ultisols

Abstract

Fifteen acid soils of Mizoram representing Ultisols and Inceptisols, and Madhya Pradesh, representing Alfisols, were studied to characterize the nature of acidity in relation to different forms of iron (Fe) and aluminum (Al). The mean contents of Fe and Al were extracted by various extracting reagents and were found to be in descending order as followed: dithionite>oxalate>pyrophosphate>ammonium acetate>KCl. The electrostatically bonded EB‐H⁺ and EB‐Al³⁺ acidity comprised 28.3 and 71.7% of exchangeable acidity whereas EB‐H⁺, EB‐Al³⁺, exchangeable, and pH‐dependent acidities comprised 9.8, 30.7, 40.5, and 59.5% of total potential acidity. All forms, of acidity showed significant correlation with pH_k and organic carbon. Among the different forms, Fe and Al caused most of the variations in different forms of soil acidity but the effect of different forms of Al are more active and directly participate in the formation of EB‐H⁺, EB‐Al³⁺, and exchangeable acidity.     

Acid and mineral components determining the exchangeable acidity in mineral horizons of taiga soils of the Komi Republic

Analysis of acid components in soil-KCl suspension filtrates from the mineral horizons was performed on the basis of analytical data reported between 1958 and 2003, including the data on more than 60 soil profiles (about 300 horizons) from the taiga zone of the Komi Republic. It was shown that the acid ions Al³⁺, H⁺ (exchangeable hydrogen), and Fe³⁺ and the basic ion H₃SiO ₄ ^? are the main components determining the pH of filtrates. Groups of horizons with the predominance of specific ions were separated.     

Biogeochemistry of two Appalachian deciduous forest sites in relation to episodic stream acidification

Bulk precipitation, throughfall, and soil water chemistry were studied from November 1983 to November 1984 at two ridge-top Appalachian deciduous forest sites to isolate causes of differing episodic stream acidification. The Fork Mountain site in West Virginia, which exhibited little episodic stream acidification, had lower deposition of H⁺ and SO _inf4 ^sup2? and greater reductions of H⁺ in the water circulating through the forest canopy, forest floor, and mineral soil than the Peavine Hill site in Pennsylvania. Greater neutralization at Fork Mountain was linked to higher Ca and Mg carbonate contents in the sandstone and shale soil parent materials. Fork Mountain had greater amounts of exchangeable bases in the organic and mineral soil horizons. Neither site appeared to be accumulating SO _inf4 ^sup2? in the soil, with Peavine Hill losing 56% more than was received in bulk deposition. Anions in soil leachate at Fork Mountain were largely balanced by Ca²⁺ and Mg²⁺, while at the Peavine Hill site A1" was the dominant cation. Results suggest that the typically-low carbonate content of sandstone and shale soil parent materials commonly found in Appalachian forests may be a key parameter controlling soil and stream acidification. Data for the one-year period also suggest bulk deposition of H⁺ was 63% greater at Peavine Hill than Fork Mountain.     

Measuring and simulating pH buffer capacity of calcareous soils using empirical and mechanistic models

ABSTRACT

We studied (i) the pH buffer capacity (pHBC) of calcareous soils varied widely in calcite and texture, (ii) the contribution of soil properties to pHBC and (iii) the significance of using a model based on calcite dissolution to estimate the pHBC of calcareous soils. The pHBC of soils was measured by adding several rates of HCl to soils (100–6500 mM H⁺ kg^–1), in a 0.01 M CaCl₂ background and an equilibration time of 24 h. The pHBC (mM H⁺ kg^–1 pH^?1) varied from 55 to 3383, with the mean of 1073. The pHBC of the soils was strongly correlated with soil CaCO₃ equivalent (calcite) (r = 0.94), sand (r = ?0.72), silt (r = 0.60), EC (r = 0.63), pH (r = 0.55), and weakly (r = 0.37) but significantly with clay content. The attained pHBC values indicated that calcite was probably the main buffer system in these soils. The chemical equilibrium model successfully predicted pH titration curves based on calcite dissolution, indicating buffering of acid inputs in the calcareous soils is dominated by calcite dissolution. The model can be used to simulate acidification of calcareous soils and to provide information for making environmental management decisions.     

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

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

pH,nitrogen mineralization,and KCl-extractable aluminum as affected by initial soil pH and rate of vetch residue application: results from a laboratory study

Purpose

Initial soil pH determines the direction and magnitude of pH change after residue addition. This study aimed to evaluate the relative importance of initial soil pH and rate of residue application in determining subsequent pH change, nitrogen (N) mineralization, and soil-exchangeable aluminum (Al).

Materials and methods

An incubation experiment was conducted for 102 days on a Plinthudult soil and a Paleudalf soil, where pH gradients were produced after application of direct current (DC). Rates of vetch applications were 0, 5, 15, 30, and 50 g kg^?1 soil.

Results and discussion

Increasing rates of vetch application caused greater increases in soil pH, but no consistent increase in soil pH at higher initial pH range (4.40～6.74), because of nitrification. There was a positive correlation between alkalinity production and the initial soil pH at day 14, while correlations became negative at days 56 and 102. Mineral N accumulated as NH₄ ⁺–N in low pH soils, due to limited nitrification, while NO₃ ^?–N dominated in higher pH soils. Application of vetch decreased KCl-extractable Al, probably because of complexation of Al by organic matter and precipitation of Al as a result of increased pH, reductions in Al concentration increased with increasing rates of vetch application. However, this amelioration effect on Al concentration weakened with time in higher pH soils.

Conclusions

Application of vetch residue can significantly increase soil pH and concentrations of mineral N and reduce exchangeable Al. These amelioration effects are enhanced with increased rate of vetch addition and vary with time depending on the initial pH of the soil.     

Acidification and salinization of soils with different initial pH under greenhouse vegetable cultivation

Purpose

Field survey and sampling of vegetable greenhouse soils were conducted in Shouguang, Shandong Province, and Ningbo, Zhejiang Province to study the acidification and salinization characteristics of soils with different initial soil pH values and greenhouse cultivation time.

Materials and methods

The pH, electrical conductivity (EC), and ion composition of 74 composite soil samples were analyzed to evaluate their relation to soil acidification and salinization.

Results and discussion

Compared with their corresponding open-field soils, acidification and salinization of the greenhouse soils occurred in both 0-20 cm and 20-40 cm soil layers for the Shouguang and Ningbo soils. The soil pH decreased gradually at different rates as greenhouse cultivation time increased in the two surveyed regions, but the opposite trend was observed for soil EC. For the Shouguang soils, while the percentages of K⁺ and NO₃ ^? increased dramatically and Ca²⁺ and HCO₃ ^- decreased significantly after the soils were converted to greenhouse use, the correlation between soil pH and EC was significant, and the stepwise multiple regression analysis further showed that there was a significant correlation between pH and the percent of Ca²⁺ and HCO₃ ^?.

Conclusions

Soil acidification and salinization are common in greenhouse soils with different initial soil pH. Soil acidification in the Shouguang soils is a result of decrease in the percent of Ca²⁺, HCO₃ ^? due to over application of N and K fertilizers. Future research should be devoted to understanding the relevant mechanisms in greenhouse soils with lower initial soil pH values to assess if there are correlations between soil acidification and salinization under greenhouse cultivation.     

Increases in pH and soluble salts influence the effect that additions of organic residues have on concentrations of exchangeable and soil solution aluminium

It has been suggested that additions of organic residues to acid soils can ameliorate Al toxicity. For this reason the effects of additions of four organic residues to an acid soil on pH and exchangeable and soil solution Al were investigated. The residues were grass, household compost, filter cake (a waste product from sugar mills) and poultry manure, and they were added at rates equivalent to 10 and 20 t ha^?1. Additions of residues increased soil pH measured in KCl (pH_(KCl)) and decreased exchangeable Al³⁺ in the order poultry manure > filter cake > household compost > grass. The mechanism responsible for the increase in pH differed for the different residues. Poultry manure treatment resulted in lower soil pH measured in water (pH_(water)) and larger concentrations of total (Al_T) and monomeric (Al_mono) Al in soil solution than did filter cake. 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. The considerably larger concentrations of soluble C in soil solution originating from the poultry manure may also have maintained greater concentrations of Al in soluble complexed form. There was a significant negative correlation (r = ?0.94) between pH_(KCl) and exchangeable Al. Concentrations of Al_T and Al_mono in soil solution were not closely related with pH or exchangeable Al. The results suggest that although additions of organic residues can increase soil pH and decrease Al solubility, increases in soluble salt and soluble C concentrations in soil solution can substantially modify these effects.     

Equilibria of weak acids and organic Al complexes explain activity of H+ and Al3+ in a salt extract of exchangeable cations

Two sequential extractions with unbuffered 0.1 m BaCl₂ were done to study the release of salt-exchangeable H⁺ and Al from mineral horizons of five Podzols and a Cambisol. Released Al was found to have a charge close to 3+ in all horizons and in both extractions. This finding was supported by the near-equality of the titrated exchangeable acidity (EA_T) and the sum of exchangeable acids (EA = H_e + 3Al_e, calculated from the pH and Al concentration of the extract). The ratio between EA of the second and the first extraction was over 0.50 in the Bs2 and C horizons and smaller in the other horizons. H⁺ was assumed to be in equilibrium with weak acid groups, and the modified Henderson–Hasselbach equation, pK_HH = pH ? n log (α/(1 ? α)), was used to explain pH of the extract. The degree of dissociation (α) was calculated as the ratio between effective and potential cation exchange capacity. Value of the empirical constant n was found to be near unity in most horizons. When the monoprotic acid dissociation was assumed in all horizons, pK_HH had the same value in both extractions. For Al³⁺, two equilibrium models were evaluated, describing (i) complexation reactions of Al³⁺ with soil organic matter, and (ii) equilibrium with Al(OH)₃. Apparent equilibrium constants were written as (i) pK_o = xpH ? pAl³⁺, and (ii) log Q_gibbs= log Al³⁺ ? 3log H^+. The two extractions gave an average reaction stoichiometry x close to 2 in all horizons. Results suggest that an equilibrium with organic Al complexes can be used to express dissolved Al³⁺, aluminium being apparently bound to bidentate sites. The value of log Q_gibbs was below the solubility of gibbsite (log K_gibbs = 8.04) in many horizons. In addition, log Q_gibbs of the second extraction was greater than that of the first extraction in all horizons except the C horizon. This indicates that equilibrium with Al(OH)₃ cannot explain dissolved Al³⁺ in the soils. We propose that the models of pK_HH and pK_o can be used to simulate exchangeable H⁺ and Al³⁺ in soil acidification models.     

Effects of biomass ash,bone meal,and alkaline slag applied alone and combined on soil acidity and wheat growth

Purpose

The purpose of this study is to examine the effects of combined application of biomass ash (BA), bone meal (BM), and alkaline slag (AS) on soil acidity, nutrient contents, uptake of the nutrients by wheat, and wheat growth.

Materials and methods

A pot experiment with an Ultisol collected from Anhui province, China, was conducted to compare the effects of BA, BM, and AS applied alone and combined on soil acidity; soil nutrient contents; uptake of N, P, K, Ca, and Mg by wheat, and wheat growth.

Results and discussion

Application of BA, BM, and AS alone and combined increased soil pH and decreased soil exchangeable Al³⁺. BA + BM + AS showed the greatest ameliorating effect on soil acidity, and soil pH of the treatment increased by 1.24 units compared with control. Application of BA + BM + AS reduced soil exchangeable Al³⁺ and increased soil exchangeable calcium and magnesium to a greater extent than BA + BM and single application of the amendments. The BM-containing amendments substantially increased soil available phosphorous by 66–93% compared with control. Application of the amendments alone and combined enhanced the uptake of N, P, K, Ca, and Mg by wheat and thus promoted wheat growth and increased yield of wheat grains. Application of BA + BM + AS and BA + BM showed greater effects on nutrient uptake and wheat growth than single application of the amendments. Wheat straw weights of the two treatments were 11.1 and 10.1 times greater than that of control. The data were 2.7, 4.8, and 5.6 times for the treatments of BA, AS, and BM. The contents of Cd, Cr, Zn, and Cu in wheat grains were lower than standard limits, except for the single BA treatment.

Conclusions

BA + BM + AS is the best choice for amelioration of acid soils and promotion of crop production.

     

Effect of low energy-consuming biochars in combination with nitrate fertilizer on soil acidity amelioration and maize growth

Purpose

We evaluated the ameliorative effects of crop straw biochars either alone or in combination with nitrate fertilizer on soil acidity and maize growth.

Materials and methods

Low energy-consuming biochars were prepared from canola and peanut straws at 400 °C for 2 h. Incubation experiment was conducted to determine application rate of biochars. Afterward, maize crop was grown in pots for 85 days to investigate the effects of 1 % biochars combined with nitrate fertilizer on soil pH, exchangeable acidity, and maize growth in an Ultisol collected from Guangdong Province, China.

Results and discussion

Application of 0.5, 1.0, and 1.5 % either canola straw biochar (CSB) or peanut straw biochar (PSB) increased soil pH by 0.15, 0.27, 0.34, and 0.30, 0.58, 0.83 U, respectively, after 65-day incubation. Soil pH was increased by 0.49, 0.72, 0.78, and 0.88 U when 1 % CSB or PSB was applied in combination with 100 and 200 mg N/kg of nitrate, respectively, after maize harvest in greenhouse pot experiment. These low-cost biochars when applied alone or in combination with nitrate not only reduced soil exchangeable acidity, but also increased Ca²⁺, Mg²⁺, K⁺, Na⁺, and base saturation degree of the soil. A total of 49.91 and 80.58 % decreases in exchangeable acidity were observed when 1 % CSB and PSB were incubated with the soil for 65 days, compared to pot experiment where 71.35, 78.64, 80.2, and 81.77 % reductions of exchangeable acidity were observed when 1 % CSB and PSB were applied in combination with 100 and 200 mg N/kg of nitrate, respectively. The higher contents of base cations (Ca²⁺, Mg²⁺, K⁺, Na⁺) in biochars also influenced the plant growth. The higher biomass in CSB-treated pots was attributed to the higher K content compared to PSB. The higher percent reduction in exchangeable Al³⁺ by applying 1 % CSB combined with 200 mg N/kg of nitrate consistently produced maximum biomass (129.65 g/pot) compared to 100 mg N/kg of nitrate and 1 % PSB combined with 100 and 200 mg N/kg of nitrate. The exchangeable Al³⁺ mainly responsible for exchangeable acidity was decreased with the application of biochars and nitrate fertilizer. A highly significant negative relationship was observed between soil exchangeable Al³⁺ and plant biomass (r ²?=?0.88, P?<?0.05).

Conclusions

The biochars in combination with nitrate fertilizer are cost-effective options to effectively reduce soil acidity and improve crop growth on sustainable basis.

     

Effects of fertilization practices on aluminum fractions and species in a wheat soil

Purpose

To better understand the effect of fertilizer practices on soil acidification and soil organic matter (SOM) stocks in a rice-wheat system, a field experiment was conducted to (i) investigate the influence of fertilizer practices on the Al forms in solid phases and the distribution of Al species in water extracts and (ii) explore the relationship between the Al forms, the quantity and composition of SOM, and soil acidity.

Materials and methods

Seven fertilizer treatments including CL (no fertilizer), NK, PK, NPK, N₂PK (PK and 125 % of N), NP₂K (NK and 125 % of P), and organic fertilizer (OF) were applied to induce various changes in pH and SOM composition (i.e., total C and N contents, C/N ratio, and SOM recalcitrant indices) in a rice-wheat system. After 6-year cultivation, different pools of Al forms (i.e., amorphous Al; organically bound Al of varying stability; exchangeable Al; water-soluble inorganic Al³⁺, Al-OH, Al-F, Al-SiO₃, and Al-SO₄; and organic Al monomers) were quantified and related with SOM composition and soil pH during the wheat phase.

Results and discussion

Fertilizer types significantly changed soil pH and SOM composition and which explained 84 % of the variance of Al forms using redundancy analysis. An interaction between soil pH and SOM quality on Al forms also existed but only accounted for a very small (6 %) portion of the variation. Compared to CL and chemical fertilizer, OF practice with relative low SOM stabilization is likely to favor the formation of amorphous Al in order to bind more SOM. The decrease in exchangeable acidity and water-extractable Al via hydroxyl-Al precipitation but not in the form of organo-aluminum complexes evidenced this phenomenon. In contrast, chemical fertilizer input increased exchangeable Al and water extract Al (especially Al³⁺), partly at the expense of organically bound Al. The destabilization of organic-aluminum complexes was a mechanism of pH buffering evidenced by the increased soluble Al-dissolved organic matter (DOM) as soil pH decreases. Further, the magnitude of this trend was much greater for elevated N input compared with P input.

Conclusions

Chemical fertilizer with relative high SOM stabilization favored the formation of exchangeable Al and soluble Al resulting in soil acidification, whereas OF with relative low SOM stabilization tended to transform exchangeable Al and soluble Al to amorphous Al, thereby alleviating soil acidification and enhancing C stocks in a rice-wheat system.

     

Acidification and liming of coniferous forest soil: Long-term effects on turnover rates of carbon and nitrogen during an incubation experiment

Forest soils from field plots, subjected to long-term acidification by H₂SO₄ treatment, or to liming, were examined for the effects of treatment on net mineralization and turnover rates of carbon and nitrogen during incubation. The total soil respiration was decreased as a result of acidification, whereas the proportion of labeled C, introduced as ¹⁴C-glucose at start of the incubation, was increased in the CO₂ pool emitted. The accumulation of mineral N (ammonium) was not significantly influenced by acidification, whereas the rate of microbial N turnover, obtained from ¹⁵N-dilution data for the exchangeable NH₄⁺ fraction, was markedly decreased.     

Salts and acids as determinants of the solution composition of acidic forest soils — anion effects

The study aimed at evaluating whether salt-induced mobilization of acidity may be modified by the type of anion. For this purpose, the effects of different neutral salts on the solution composition of acid soils were investigated. The results were compared with those of the addition of acids. Two topsoil (E and A) and two subsoil horizons (Bs and Bw) were treated with NaCl, Na₂SO₄, MgCl₂, MgSO₄, HCl, and H₂SO₄ at concentrations ranging from 0 to 10 mmol dm^?3. With increasing inputs of Cl^? the pH of the equilibrium soil solution dropped, the concentrations of Al and Ca increased, and the molar Ca/(Al³⁺ + AlOH²⁺ + Al(OH)₂⁺) ratios decreased. These effects were the least pronounced when NaCl was added and the most at the HCl treatments. According to the release of acidity, the topsoils were more sensitive for salt-induced soil solution acidification whereas on base of the molar Ca/(Al³⁺ + AlOH²⁺ + Al(OH)₂⁺) ratios, the salt effect seems to be more important for the subsoils. Addition of S0₄^2? salts and H₂SO₄ induced higher pH and lower Al concentrations than the corresponding Cl^? treatments due to the SO₄^2? sorption, especially in the subsoils. The Ca/(Al³⁺ + AlOH²⁺ + Al(OH)₂⁺) ratios were higher than those of the corresponding Cl^? treatments. In subsoils even after H₂SO₄ additions these ratios were not higher than those of the NaCl treatments. The results indicate (I) that speculation about the effects of episodic salt concentrations enhancement on soil solution acidification not only need to consider the ionic strength and the cation type but also the anion type, (II) that salt-induced soil solution composition may be more crucial in subsoils than in topsoils, and (III) that in acid soils ongoing input of HNO₃ due to the precipitation load may induce an even more acidic soil solution than the inputs of H₂SO₄ of the last decade.     

Effects of Alum-treated Waste Water Sludge on Barley Growth

Alum sludge derived from a municipal wastewater plant was used as a soil amendment in a greenhouse study with barley (Hordeum vulgare) as the test crop. Treatment variables included the soil pH (4.5, 5.1 and 6.5), the amount of Al in the sludge (control = 30 mg Al_T/g; alum sludges = 38 and 52 mg Al_T/g), and the sludge application rate (100 and 270 kg N_T/ha). Soil amendment with the two alum sludges reduced soil pH, increased Al³⁺ activity in the soil solution, and reduced barley growth over the 6-week experiment. Barley growth decreased as the Al³⁺ activity in the sludged soil solution increased, but for a given Al³⁺ the phytotoxicity of Al was markedly pH dependent. For example, at a pH of 5.0 ± 0.1 an Al³⁺ activity of 0.5 μM was sufficient to inhibit plant growth by about 50% this IC₅₀ value increased five-fold to about 2.5 μM when the soil pH was 4.5 ± 0.1. This decrease in the toxicity of Al50 with acidification was explained in terms of a competitive interaction between the H⁺-ion and Al³⁺ at the root surface. Stepwise multiple regression allowed the prediction of aerial leaf biomass from soil pH and sludge application rate.     

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.     

Correlations between different acidity forms in amorphous loamy soils of the tundra and taiga zones

Pair correlation coefficients (r) between the acidity parameters for the main genetic horizons of soddy-podzolic soils (SPSs), typical podzolic soils (TPSs), gley-podzolic soils (GPSs), and tundra surfacegley soils (TSGSs) have been calculated on the basis of a previously developed database. A significant direct linear correlation has been revealed between the pH_water and pH_KCl values in the organic and eluvial horizons of each soil, but the degree of correlation decreased when going from the less acidic SPSs to the more acidic soils of other taxons. This could be related to the fact that, under strongly acid conditions, extra Al³⁺ was dissolved in the KCl solutions from complex compounds in the organic horizons and from Al hydroxide interlayers in the soil chlorites. No significant linear correlation has been found between the exchangeable acidity (H _exch) and the activity of the [H]⁺ ions in the KCl extract (a(H⁺)_KCl) calculated per unit of mass in the organic horizons of the SPSs, but it has been revealed in the organic horizons of the other soils because of the presence of the strongest organic acids in their KCl extracts. The high r values between the H _exch and a(H⁺)_KCl in all the soils of the taiga zones have been related to the common source and composition of the acidic components. The correlation between the exchangeable and total (H _tot) acidities in the organic horizons of the podzolic soils has been characterized by high r values because of the common source of the acidity: H⁺ and probably Al³⁺ ions located on the functional groups of organic acids. High r values between the H _exch and a(H⁺)_KCl have been observed in the mineral horizons of all the soils, because the Al³⁺ hydroxo complexes occurring on the surface and in the interlayer spaces of the clay minerals were sources of both acidity forms.