Nitrification,acidification, and nitrogen leaching from subtropical cropland soils as affected by rice straw-based biochar: laboratory incubation and column leaching studies

Purpose

Few studies have examined the effects of biochar on nitrification of ammonium-based fertilizer in acidic arable soils, which contributes to NO₃ ^? leaching and soil acidification.

Materials and methods

We conducted a 42-day aerobic incubation and a 119-day weekly leaching experiment to investigate nitrification, N leaching, and soil acidification in two subtropical soils to which 300 mg N kg^?1 ammonium sulfate or urea and 1 or 5 wt% rice straw biochar were applied.

Results and discussion

During aerobic incubation, NO₃ ^? accumulation was enhanced by applying biochar in increasing amounts from 1 to 5 wt%. As a result, pH decreased in the two soils from the original levels. Under leaching conditions, biochar did not increase NO₃ ^?, but 5 wt% biochar addition did reduce N leaching compared to that in soils treated with only N. Consistently, lower amounts of added N were recovered from the incubation (KCl-extractable N) and leaching (leaching plus KCl-extractable N) experiments following 5 wt% biochar application compared to soils treated with only N.

Conclusions

Incorporating biochar into acidic arable soils accelerates nitrification and thus weakens the liming effects of biochar. The enhanced nitrification does not necessarily increase NO₃ ^? leaching. Rather, biochar reduces overall N leaching due to both improved N adsorption and increased unaccounted-for N (immobilization and possible gaseous losses). Further studies are necessary to assess the effects of biochar (when used as an addition to soil) on N.     

Critical loads for nitrogen deposition on forest ecosystems

Critical loads for N deposition are derived from an ecosystem's anion and cation balance assuming that the processes determining ecosystem stability are soil acidification and nitrate leaching. Depending on the deposition of S, the parent soil material, and the site quality critical N deposition rates will range between 20 to 200 mmol m^?2 yr^?1 (3 to 14 kg ha^?1 yr^?1) on silicate soils and reach 20 to 390 mmol m^?2 yr^?1 (3 to 48 kg ha^?1) on calcareous soils.     

Nitrification and Methane Oxidation in Forest Soil: Acid Deposition, Nitrogen Input and Plant Effects

In a laboratory incubation experiment, nitrification potential, methane oxidation, N₂O and CO₂ release were studied in the organic soil layer (0–10 cm) of field lysimeters containing re-established soil profiles from a 100-year-old Scots pine (Pinus sylvestris) forest of Norway. The experiment was designed as a full factorial (3 factors; N fertilisation rates, soil acidification, and plants), with three replicates. The more acidic irrigation (pH 3) significantly reduced nitrification potential and N₂O fluxes, methane oxidation and CO₂ release. We concluded that the reduction in soil N₂O release by severe acid deposition is partly due to reduction in nitrification potential. The highest N₂O fluxes were observed in the combination of fertilised planted and less acidic pH treatment. N fertilisation (90 kg N ha^?1 y^?1 with NH₄NO₃) increased soil N₂O release by a factor of 8 and decreased CH₄ oxidation by 60–80%. Plant effects on soil nitrification potential and methane oxidation rates are discussed.     

Response of spodic B horizons to acid precipitation in northernmost Fennoscandia

In northernmost Fennoscandia there is concern about the possible environmental effects of the sulphur emissions from Russian nickel smelters on the Kola Peninsula. The purpose of this study was to investigate to what extent the soils of this region may delay the response to pH changes through sulphate adsorption, and whether there are evidence for strong soil acidification effects. To this end 26 spodic B horizons were collected along a transect from northernmost Sweden to north-easternmost Norway, only 10 km from the Pechenganikel smelter. As the pH(H₂O) was > 4.8 in all soils, and as the exchangeable Ca/Al ratio was high, there were no evidence for strong soil acidification effects. Water-extractable SO₄ was clearly affected by the S deposition and thus SO₄ was at least partly mobile in the soils; it is therefore possible that soil solutions close to the smelter may have been acidified. In spite of this, sulphate adsorption was found to be more important than cation exchange reactions as a delaying process against soil acidification, at least in the top 10 cm of the B horizon. For the top 20 cm of the B horizon it was estimated that S04 adsorption can neutralize, on average, 700 mmol_c, m^?2 of acid before the pH is decreased to 4.4. Thus if the S deposition remains unchanged, decades are required to severely acidify most soils in the affected parts of Norway and Finland.     

Ion leaching from a sugar maple forest in response to acidic deposition and nitrification

Year-to-year variation in acidic deposition within a mature sugar maple-dominated forest and in leaching of ions from the associated podzolic soil were examined at the Turkey Lakes Watershed between 1981 and 1986. Below-canopy inputs to the soil of SO₄ ^2? and NO₃ ^? in throughfall averaged 640 and 295 eq. ha^?1 yr^?1; the corresponding ranges were 493–917 and 261–443 eq. ha^?1 yr^?1. The contribution of atmospheric deposition to SO₄ ^2? NO₃ ^? and Ca²⁺ leaching decreased over the six years. During the study period, the mean annual volume-weighted NO₃ ^? concentration decreased in throughfall and forest-floor percolate and increased in the mineral-soil solution collected below the effective rooting zone. A substantial shift in the balance between SO₄ ^2? and NO₃ ^?leaching from the mineral soil was observed; leaching of SO₄ ^2?decreased and NO₃ ^? leaching increased with time. Leaching of Ca²⁺ and Mg²⁺ from the soil was increased as a result of excess NO₃ ^? production in the soil. The calculated output of NO₃ ^? from the soil, which averaged 1505 eq. ha^?1 yr^?1, considerably exceeded the atmospheric deposition of NO₃ ^?, whereas SO₄ ^2? outputs were only moderately greater than inputs.     

Temporal and Spatial Variations in Soil Water Chemistry at Three Acid Forest Sites

As acid deposition declines, recovery from acidification is delayed by the fact that the soil processes that earlier buffered against acidification are now being reversed. Monitoring of within catchment processes is thus desirable. However, soil sampling is destructive and not suitable for long-term monitoring at a single site, whereas sampling of soil water with suction lysimeters may be more suitable. In this paper we evaluate 8–11 years of soil water chemistry from E- and B-horizons in three acid forest soil plots within monitored catchments. Five years of sampling also included the C-horizon. To our knowledge, this is the first long-term lysimeter study including the E-horizon showing recovery from acidification, and one of few studies including the B-horizon. Soil water concentrations of SO₄ decreased significantly between –9.5 and –1.4 μeq L^-1 yr^-1, with much higher rates of change at two southern sites compared to a northern site, where levels and changes of deposition were lower. The average annual bulk deposition of S ranged between 3 kg S ha^-1 at the northernmost site to 11 kg S ha^-1 at the southernmost site. The SO₄ decline in E-horizons was smaller than the decline in deposition, which indicated leaching of SO₄ from the O-horizon. At the two southern sites, a weaker decline in SO₄ in the B-horizon compared to the E-horizon indicated desorption of SO₄. The negative trends in SO₄ were to a large extent balanced by decreases in base cations but there were also tendencies of recovery from acidification in soil solution at the southern sites by increasing pH and ANC. However, these were contradicted by increasing Al concentrations. A high influence of marine salts in the early 1990s may have delayed the recovery. Decreasing trends of the Ca/(H⁺)² ratio in the soil solution, most pronounced at one of the southern sites, suggested that the soils were becoming more acidic, although the soil solution tended to recover.     

Ozone,acidic precipitation,and soil Mg impacts on soil and loblolly pine seedling nutrient status after three growing seasons

Recent studies have suggested that the growth of loblolly pine (Pinus taeda L.) has declined in the southeastern United States, possibly due to acidic deposition and air pollutants, especially under conditions of low nutrient availability. Consequently, the potential for individual and synergistic impacts of O₃, acidic precipitation, and soil Mg status on the nutrient status of loblolly pine seedlings and soil was investigated over a 3 yr study period. Thirty-six open top chambers equipped with a rainfall exclusion/addition system were utilized to administer three levels of O₃ (subambient, ambient, or twice ambient) and two acidic precipitation treatments (pH 3.8 or 5.2) to seedlings growing in 24-L plastic pots containing soil having either 35 or 15 mg kg^?1 of exchangeable Mg. Each chamber contained 36 pots, and each treatment combination was replicated six times for a total of 1296 individual pots. After three seasons, throughfall and foliar nutrition data indicated that foliar leaching was not accelerated by increasing the acidity of precipitation from pH 5.2 to 3.8 and that increasing O₃ did not act to exacerbate foliar leaching. Further, foliar nutrient concentrations were not significantly affected by precipitation pH or O₃ treatments. Soil and soil solution data also indicate no accelerated soil leaching associated with chronic acidic precipitation. Differences in soil Mg treatments were reflected in soil solution and seedling Mg contents, but the 15 mg kg^?1 soil Mg treatment was not sufficiently low enough to induce Mg deficiency in the seedlings.     

Lysimeter study with a cambic Arenosol exposed to artificial acid rain: I. Concentrations of ions in leachate

The effects of artificial acid rain on soil leachate composition were studied in a lysimeter experiment. Cambic Arenosol (Typic Udipsamment) in monolith lysimeters was treated for 6 1/2 yr with 125 mm yr^?1 artificial rain in addition to natural precipitation. Artificial acid rain was produced from groundwater with H₂SO₄ added. pH levels of 6.1, 4 and 3 were used. Increasing content of H₂SO₄ in the artificial rain increased the concentration of Ca²⁺ and Mg²⁺ in the leachate significantly. The pH of the leachate was slightly reduced only by the most acidic treatment (pH 3). The H^+? retention was not accompanied by a proportionate increase in the Al ion concentration. A slight increase in the Al ion concentration was only observed in the leachate from the pH 3-treated lysimeter. We conclud that cation exchange and/or weathering were the main buffer mechanisms in the soil. The study supports conclusions from other acidification studies, that acidic precipitation is likely to increase the leaching of Ca²⁺ and Mg²⁺ from soils.     

One equation to analyse the pH of soil systems

Starting from the basic equations of chemical equilibrium, an analytical mathematical expression is derived that relates pH to base saturation, concentration of acid anions (SO₄^2?, NO₃^?, etc.) and other properties of the soil and soil solution. The equation is particularly valid in acid soils (low base saturation and relatively large, >100 μmol_c dm^?3, concentration of acid anions) in the range in which cation exchange is the buffering mechanism. Values of pH, alkalinity and degassed pH calculated with the aid of this equation compared well to values measured in three forest-floor horizons; calculated pH values also compared well to values measured on a number of acid soils. The equation is also used to derive analytical mathematical expressions for alkalinity, soil leaching sensitivity (a measure of the sensitivity of a soil solution to become dominated by A1³⁺), and other variables of interest in the context of acidification.     

Impacts of acid precipitation on coniferous forest ecosystems

This paper summarizes the results from current studies in Norway. One main approach is the application of artificial acid ‘rain’ and of lime to field plots and lysimeters. Application during two growth seasons of 50 mm mo^?1 of ‘rain water’ of pH 3 to a podzol soil increased the acidity of the humus and decreased the base saturation. The reduction in base saturation was mainly due to leaching of Ca and Mg. Laboratory experiments revealed that decomposition of pine needles was not affected by any acid ‘rain’ treatment of the field plots. Liming slightly retarded the decomposition. No nitrification occurred in unlimed soils (pH 4.4-4.1). Liming increased nitrification. The soil enchytraeid (Ohgochaeta) fauna was not much affected by the acidification. Germination of spruce seeds in acidified mineral soil was negatively affected when soil pH was 4.0 or lower. Seedling establishment was even more sensitive to increasing soil acidity. Analysis of throughfall and stemflow water in southernmost Norway reveals that the total deposition of H₂SO₄ beneath spruce and pine is approximately two times the deposition in open terrain. A large part of this increase is probably due to dry deposition. Increased acidity of the rain seems to increase the leaching of cations from the tree crowns. Tree-ring analysis of spruce (Picea abies (L.) Karst.) and pine (Pinus sylvestris L.) has been based on comparisons between regions differently stressed by acid precipitation and also between sites presumed to differ in sensitivity to acidification. No effect that can be related to acid precipitation has yet been detected on diameter growth.     

Identifying sources of snowmelt acidification with a watershed mixing model

We used ionic tracers to estimate the volume of old (soil and ground) water interacting with snowmelt in eleven Adirondack, NY watersheds. The contribution of old water varied from 66 to 90%, with no general relationship between old water % and soil depth to till. This approach also discriminated between watershed retention and release of particular ions to lake outlet water during snowmelt. Most watersheds released NO₃ ^? during snowmelt, in addition to the snowpack NO₃ ^?. Nitrification of snowpack NH₄ ⁺ explained part of the additional NO₃ ^? in lake out outlet water, but some NO₃ ^? was likely mineralized nitrogen from soil organic matter. All watersheds retained NH₄ ⁺ as well. Nitrogen release was greatest in the acidic watersheds in the southwestern Adirondacks, a region thought to be impacted by anthropogenic deposition. During snowmelt, Ca²⁺ and Mg²⁺ ions (presumably from soil exchange sites) were also released from most watersheds. In watersheds with acidic (minimum pH<4.6) lake outlet water, Al was also released during snowmelt. Thus, lake outlet water acidification during snowmelt was both buffered by cation release, and intensified by NO₃ ^? release. If the soil exchangeable cation pools were not replenished prior to snowmelt, or NO₃ ^? mobilization were increased, acidification during snowmelt would intensify.     

Sensitivity of Scottish Upland Moorland Podzols Derived from Sandstones and Quartzites to Acidification: the Potential Importance of the Mobile Anion Effect

Soil samples were collected from the main horizons of Scottish upland moorland podzols derived from quartzite or Devonian and Torridonian sandstones. The soils were subjected to routine chemical analysis and the results studied in relation to potential acidification effects of atmospheric deposition. Stronger correlations were observed for soil pH_water than for soil pH in CaCl₂ with wet deposition fluxes of mobile strong-acid anions. Exchangeable Al³⁺ correlated more strongly with wet deposition fluxes of mobile strong-acid anions than with H⁺ deposition flux. It is suggested that the direct effects of mobile anion enhancement upon soil pH_water must be taken into account when assessing damage to, and hence critical loads of, acidification-sensitive mineral soils.     

Nitrification and acidification from urea application in red soil (Ferralic Cambisol) after different long-term fertilization treatments

Purpose

Long-term manure applications can prevent or reverse soil acidification by chemical nitrogen (N) fertilizer. However, the resistance to re-acidification from further chemical fertilization is unknown. The aim of this study was to examine the effect of urea application on nitrification and acidification processes in an acid red soil (Ferralic Cambisol) after long-term different field fertilization treatments.

Materials and methods

Soils were collected from six treatments of a 19-year field trial: (1) non-fertilization control, (2) chemical phosphorus and potassium (PK), (3) chemical N only (N), (4) chemical N, P, and K (NPK), (5) pig manure only (M), and (6) NPK plus M (NPKM; 70 % N from M). In a 35-day laboratory incubation experiment, the soils were incubated and examined for changes in pH, NH₄ ⁺, and NO₃ ^?, and their correlations from urea application at 80 mg N kg^?1(?80) compared to 0 rate (?0).

Results and discussion

From urea addition, manure-treated soils exhibited the highest acidification and nitrification rates due to high soil pH (5.75–6.38) and the lowest in the chemical N treated soils due to low soil pH (3.83–3.90) with no N-treated soils (pH 4.98–5.12) fell between. By day 35, soil pH decreased to 5.21 and 5.81 (0.54 and 0.57 unit decrease) in the NPKM-80 and M-80 treatments, respectively, and to 4.69 and 4.53 (0.43 and 0.45 unit decrease) in the control-80 and PK-80 treatments, respectively, with no changes in the N-80 and NPK-80 treatments. The soil pH decrease was highly correlated with nitrification potential, and the estimated net proton released. The maximum nitrification rates (K _max) of NPKM and M soils (14.7 and 21.6 mg N kg^?1 day^?1, respectively) were significantly higher than other treatments (2.86–3.48 mg N kg^?1 day^?1). The priming effect on mineralization of organic N was high in manure treated soils.

Conclusions

Field data have shown clearly that manure amendment can prevent or reverse the acidification of the red soil. When a chemical fertilizer such as urea is applied to the soil again, however, soil acidification will occur at possibly high rates. Thus, the strategy in soil N management is continuous incorporation of manure to prevent acidification to maintain soil productivity. Further studies under field conditions are needed to provide more accurate assessments on acidification rate from chemical N fertilizer applications.     

A preliminary assessment of nitrogen-based fresh water acidification in southeastern Canada

Sulphate deposition is the primary cause of acidification in northeastern North America, and new SO₂ emission control is being implemented. However, continuation of existing levels of N deposition may undermine the environmental benefits derived from SO₂ control. This likelihood has been assessed for Canadian lakes. Maximum N deposition (～13 kg N ha^?1 yr^?1) occurs in south-central Ontario and southwestern Quebec. Regional median NO ₃ ^? levels are generally low (<5 μeq L^?1) suggesting that on average, N-based acidification is minor compared to the S-based component. However, examination of the seasonal NO ₃ ^? pattern at 5 intensively monitored basins reveals that 2 of them (in Ontario and Quebec) have incipient N saturation. A regional status for nitrogen-based acidification was qualitatively assessed by classifying survey data to identify cases of NO ₃ ^? leaching. Many lakes throughout southeastern Canada exhibit some leaching, particularly those in south-central Ontario and southwestern Quebec. While the evidence for a deposition-acidification link appears strong, sources of N other than the atmosphere should be considered for certain anomalous cases.     

Soil ecological study on dynamics of K,Mg, and Ca,and soil acidity in shifting cultivation in Northern Thailand

Abstract

Soil degradation caused by excessive land use is presently one of the major constraints on sustainable agriculture in the mountainous area of northern Thailand. In order to obtain basic information about soil fertility problems involved in the transition from traditional shifting cultivation to more intensive upland farming, the dynamics of K, Mg, and Ca, and soil acidity in the farming systems of both Karen and Hmong/Thai peoples were investigated. In the fields that lay fallow for more than 5 y, the soils were highly acidic and poor in exchangeable bases, mainly due to the fact that the fallow vegetation rapidly absorbed inorganic bases (K, Mg, and Ca) in the soils. In the fields both under fallow and cropping within 3 y after the slash and burn practice, the high acidity observed in the soils at the fallow stage seemed to be alleviated by ash input with high alkalinity. The aboveground biomass ranged from 9 to 10 t ha^?1 in the 8 y fallow field and the sum of inorganic bases and alkalinity, which were expected to be added to the soils with ash input, ranged from 3 to 4 kmol( + ) ha^?1 or kmol(-) ha^?1 , respectively. In the fields under continuous cultivation for more than 4 y after the slash and burn practice, the subsoils showed a more acidic nature than in the fields immediately after burning. Judging from the high concentrations of inorganic bases in the soil solution from the subsoils, the decrease of the content of exchangeable bases and resulting soil acidification might have proceeded through leaching loss of these bases. Among the exchangeable bases in the soils, Ca and Mg were generally predominant and K occurred as trace. Comparison of the total contents of the bases with the contents of exchangeable ones showed that most of Ca occurred in an exchangeable form while most of K and Mg occurred in the nonexchangeable forms in the soils. Therefore, Ca was likely to be readily depleted along with soil acidification in continuous cultivation.     

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.     

Natural and anthropogenic components of soil acidification

The following 8 theses are theoretically founded and experimentally quantified. 1. Rocks contain only bases and no acid precursors. Therefore, with the exception of sulfide containing rocks, soils cannot acidify as a result of atmospheric rock weathering. 2. A consumption of protons in rocks and soils results in a decrease of their acid neutralizing capacity (ANC) and can result in the buildup of a base neutralizing capacity (BNC). Strong soil acidification leads to the formation of stronger acids from weaker acids in the solid phase; this may be connected with a decrease in the BNC. 3. Weak acids (carbonic acid) lead in geological times to the depletion of bases without a larger accumulation of labile cation acids. Strong acids (HNO₃, organic acids, H₂SO₄) can lead within a few decades to soil acidification, i.e. to leaching of nutrient cations and the accumulation of labile cation acids. 4. The acid input caused by the natural emission of SO₂ and NO_x can be buffered by silicate weathering even in soils low in silicates. 5. The cause of soil impoverishment and soil acidification is a decoupling of the ion cycle in the ecosystem. 6. Acid deposition in forest ecosystems which persists over decades leads to soil acidification. 7. Formation and deposition of strong acids with conservative anions (SO₄, NO₃) shifts soil chemistry into the Al or Al/Fe buffer range up to great soil depth. In such soils eluvial conditions prevail throughout the solum and even in upper part of the C horizon: in connection with the decomposition of clay minerals, Al and eventually Fe are being eluviated. The present soil classification does not include this soil forming process. 8. In the long run, soil acidification by acid deposition results in the retraction of the root system of acid tolerant tree species from the mineral soil, and in water acidification.     

A lysimeter study of nitrate leaching from grazed grassland as affected by a nitrification inhibitor,dicyandiamide, and relationships with ammonia oxidizing bacteria and archaea

Nitrate (NO₃^?) can contribute to surface water eutrophication and is deemed harmful to human health if present at high concentrations in the drinking water. In grazed grassland, most of the NO₃^?‐N leaching occurs from animal urine‐N returns. The objective of this study was to determine the effectiveness of a nitrification inhibitor, dicyandiamide (DCD), in decreasing NO₃^? leaching in three different soils from different regions of New Zealand under two different rainfall conditions (1260 mm and 2145 mm p.a.), and explore the relationships between NO₃^?‐N leaching loss and ammonia oxidizing bacteria (AOB) and ammonia oxidizing archaea (AOA). The DCD nitrification inhibitor was found to be highly effective in decreasing NO₃^?‐N leaching losses from all three soils under both rainfall conditions. Total NO₃^?‐N leaching losses from the urine patch areas were decreased from 67.7–457.0 kg NO₃^?‐N/ha to 29.7–257.4 kg NO₃^?‐N/ha by the DCD treatment, giving an average decrease of 59%. The total NO₃^?‐N leaching losses were not significantly affected by the two different rainfall treatments. The total NO₃^?‐N leaching loss was significantly related to the amoA gene copy numbers of the AOB DNA and to nitrification rate in the soil but not to that of the AOA. These results suggest that the DCD nitrification inhibitor is highly effective in decreasing NO₃^? leaching under these different soil and rainfall conditions and that the amount of NO₃^?‐N leached is mainly related to the growth of the AOB population in the nitrogen rich urine patch soils of grazed grassland.     

Aluminium sulphate solubility in acid forest soils in Denmark

Ion leaching in 3 sandy spruce forest soils of different origin and pH was investigated in the laboratory. Zero-tension lysimeters containing undisturbed soil columns of varying soil depth were subjected to H₂SO₄ loadings for a period of 9 weeks. The analysis of the resulting leachate supports the hypothesis that Al-sulphate minerals may form in acidic soils when exposed to acid (H₂SO₄) deposition. In the B horizon of a glaciofluvial sandy soil (pH 4.2), both H⁺ and sulphate ions were retained to maintain 2pH + PSO₄ = 11.9 in the leachate solutions. This relation between H⁺ and sulphate activity may be due to an adsorption mechanism or a precipitation mechanism. The precipitation mechanism is favored by the good fit of leachate composition to the conditions for jurbanite [AlOHSO₄] formation from gibbsite [Al(OH)₃]. In the B horizon of a sandy till at pH 3.7, the Al in soil solution (0.5 mmol L^?1) was leached with sulphate. As the sulphate load was increased, some sulphate was retained. This may also be due to the dissolution and precipitation of an Al-sulphate mineral. The ion activity products of leachate solutions from the B horizon of this soil were close to the pK_s reported for jurbanite. The conditions for the possible existence and/or formation of Al-sulphate minerals in acidic soils are discussed.     

The impacts of atmospheric n inputs on throughfall,soil and stream water interactions for different aged forest and moorland catchments in Wales

A study of inorganic-N concentrations in streams, soil waters, throughfall and rainfall was conducted for one year in five moorland and 20 Sitka spruce plantation catchments in upland Wales. The forest ages ranged from 10 to 55 yr. Highly significant positive relationships with forest stand age existed for inorganic-N concentrations in streamwater, B and O horizon soil waters and throughfall. Inorganic-N in streams and B horizon waters was entirely NO₃ ^?. Inorganic-N fluxes in throughfall also showed a significant, positive relationship with stand age. Throughfall flux of inorganic-N in the oldest stand was 25.1 kgN ha^?1 yr^?1, double that in incident rainfall. The older forest stands appear unable to utilise the available N. Nitrification is very active in the soils of these older stands, resulting in significant soil acidification. The processes responsible for the observed NO₃ ^? leaching losses, and the implications for the debate on Nitrogen Critical Loads are discussed.