Organic carbon stocks and soil erodibility in Canary Islands Andosols

Soil organic carbon (SOC) plays a key role in the structural stability of soils and in their resistance against erosion. However, and as far as andic soils are concerned, these mechanisms and processes, as well as the influence of the different types of SOC on aggregate stability, are not fully understood. The targets of this paper are: (i) to determine the content and forms of SOC in Andosols under evergreen forest vegetation [laurel (Laurus) and heather (Erica) forest] and (ii) to find out the role of soil organic matter (SOM) in the aggregate stability and in the resistance of Andosols to water erosion. Soil samples have been collected in 80 sites in a 40 km² area under udic soil moisture regime. In them, fulvic and humic acids, Walkley–Black SOC, pyrophosphate-extractable SOC, Fe and Al, potassium sulphate extractable SOC, dissolved SOC, acid oxalate-extractable Fe, Al and Si, USLE K-factor and aggregate stability have been determined. The Andosols over volcanic ash are Aluandic Andosols (non-allophanic Andosols), whereas over basaltic lava flows are Silandic Andosols (allophanic Andosols). The surface (0–30 cm) samples analyzed contain 9.5–30 kg C m^− 2 being significantly higher in allophanic Andosols (p < 0.5). Organic carbon adsorbed onto the mineral fraction (extractable pyrophosphate, C_p) accounts for 35–55% of the total SOC. All samples show a high stability to slaking and raindrop impact, being the first one highly correlated (r = 0.6) with pyrophosphate extractable C (C_p), Fe (Fe_p), and Al (Al_p) in allophanic Andosols, unlike non-allophanic ones. The stability to raindrop impact correlates with pyrophosphate extractable C (C_p) and Fe (Fe_p) in both types of soils (r = 0.3–0.6, p < 0.05). These findings suggest that the high stability to both slaking and water-drop impact is due to the occurrence of allophane–Fe–OC complexes, rather than to the total OC, and the active Fe and Al forms, generated by the weathering of volcanic materials, constitute an essential constituent responsible for C sequestration and resistance to degradation in these soils.     

Secondary salinity effects on soil microbial biomass

Secondary soil salinilization is a big problem in irrigated agriculture. We have studied the effects of irrigation-induced salinity on microbial biomass of soil under traditional cotton (Gossypium hirsutum L.) monoculture in Sayhunobod district of the Syr-Darya province of northwest Uzbekistan. Composite samples were randomly collected at 0–30 cm depth from weakly saline (2.3 ± 0.3 dS m⁻¹), moderately saline (5.6 ± 0.6 dS m⁻¹), and strongly saline (7.1 ± 0.6 dS m⁻¹) replicated fields, 2-mm sieved, and analyzed for pH, electrical conductivity, total C, organic C (C_Org), and extractable C, total N and P, and exchangeable ions (Ca²⁺, Mg²⁺, K⁺, Na⁺, Cl⁻, and CO₃²⁻), microbial biomass (C_mic). The Na⁺ and Cl⁻ concentrations were 36-80% higher in strongly saline compared to weakly saline soil. The C_Org concentration was decreased by 10% and C_Ext by 40% by increasing soil salinity, whereas decrease in C_mic ranged from 18-42% and the percentage of C_Org present as C_mic from 8% to 26%. We conclude that irrigation-induced secondary salinity significantly affects soil chemical properties and the size of soil microflora.     

Arsenic Chemistry in Soils: An Overview of Thermodynamic Predictions and Field Observations

Published information, both theoretical and experimental, on As chemical behavior in soils is reviewed. Because of many emission sources, As is ubiquitous. Thermodynamic calculations revealed that As(V) species (HAsO ₄ ^2- >H₂AsO ₄ ^- at pH 7) are more abundant in soil solutions that are oxidized more than pe+pH>9. Arsenic is expected to be in As(III) form (HAsO ₂ ⁰ =H₃AsO ₃ ⁰ >AsO ₂ ^- =H₂AsO ₃ ^- at pH 7) in relatively anoxic soil solutions with pe+pH<7. Adsorption on soil colloids is an important As scavenging mechanism. The adsorption capacity and behavior of these colloids (clay, oxides or hydroxides surfaces of Al, Fe and Mn, calcium carbonates, and/or organic matter) are dependent on ever-changing factors, such as hydration, soil pH, specific adsorption, changes in cation coordination, isomorphous replacement, crystallinity, etc. Because of the altering tendencies of soil colloids properties, adsorption of As has become a complex, empirical, ambiguous, and often a self contradicting process in soils. In general, Fe oxides/hydroxides are the most commonly involved in the adsorption of As in both acidic and alkaline soils. The surfaces of Al oxides/hydroxides and clay may play a role in As adsorption, but only in acidic soils. The carbonate minerals are expected to adsorb As in calcareous soils. The role of Mn oxides and biogenic particles in the As adsorption in soils appears to be limited to acidic soils. Kinetically, As adsorption may reach over 90% completion in terms of hours. Precipitation of a solid phase is another mechanism of As removal from soil solutions. Thermodynamic calculations showed that in the acidic oxic and suboxic soils, Fe-arsenate (Fe₃(AsO₄)₄)₂) may control As solubility, whereas in the anoxic soils, sulfides of As(III) may control the concentrations of the dissolved As in soil solutions. In alkaline acidic oxic and suboxic soils, precipitation of both Fe- and Ca-arsenate may limit As concentrations in soil solutions. Field observations suggest that direct precipitation of discrete As solid phases may not occur, except in contaminated soils. Chemisorption of As oxyanions on soil colloid surfaces, especially those of Fe oxide/hydroxides and carbonates, is believed to a common mechanisms for As solid phase formation in soils. It is suggested that As oxyanions gradually concentrate on colloid surfaces to a level high enough to precipitate a discrete or mixed As solid phase. Arsenic volatilization is another As scavenging mechanism operating in soils. Many soil organisms are capable of converting arsenate and arsenite to several reduced forms, largely methylated arsines which are volatile. These organisms may generate different or similar biochemical products. Methylation and volatilization of As can be affected by several biotic (such as type of organisms, ability of organism for methylation, etc.) and abiotic factors (soil pH, temperature, redox conditions, methyl donor, presence of other ions, etc.) factors. Information on the rate of As biotransformations in soils is limited. In comparison to the biologically assisted volatilization, the chemical volatilization of As in soils is negligible.     

Sodium hypochlorite oxidation reduces soil organic matter concentrations without affecting inorganic soil constituents

Oxidative treatment can isolate a stable organic matter pool in soils for process studies of organic matter stabilization. Wet oxidation methods using hydrogen peroxide are widely used for that purpose, but are said to modify poorly crystalline soil constituents. We investigated the effect of a modified NaOCl oxidation (pH 8) on the mineral composition of 12 subsoils (4.9–38.2 g organic C kg^?1) containing varying amounts of poorly crystalline mineral phases, i.e. 1.1–20.5 g oxalate‐extractable Fe kg^?1, and of different phyllosilicate mineralogy. Post‐oxidative changes in mineral composition were estimated by (i) the determination of elements released into the NaOCl solution, (ii) the difference in dithionite‐ and oxalate‐extractable Si, Al and Fe, and (iii) the specific surface areas (SSAs) of the soils. The NaOCl procedure reduced the organic C concentrations by 12–72%. The amounts of elements released into the NaOCl extracts were small (≤ 0.14 g kg^?1 for Si, ≤ 0.13 g kg^?1 for Al, and ≤ 0.03 g kg^?1 for Fe). The SSA data and the amounts of dithionite‐ and oxalate‐extractable elements suggest that the NaOCl oxidation at pH 8 does not attack pedogenic oxides and hydroxides and only slightly dissolves Al from the poorly crystalline minerals. Therefore, we recommend NaOCl oxidation at pH 8 for the purpose of isolating a stable organic matter pool in soils for process studies of organic matter stabilization.     

The effect of soil pH manipulation on chemical properties of an agricultural soil from northern Idaho

Abstract

Selected chemical properties of an artificially acidified agricultural soil from northern Idaho were evaluated in a laboratory study. Elemental S and Ca(OH)₂were used to manipulate the soil pH of a Latahco silt loam (fine‐silty, mixed, frigid Argiaquic Xeric Argialboll), which had an initial pH of 5.7. A 100 day incubation period resulted in a soil pH manipulation range of 3.3 to 7.0. Chemical properties evaluated included: N mineralization rate, extractable P, AI, Mn, Ca, Mg and K and CEC. N mineralization rate (assessed by anaerobic incubation) decreased with decreasing soil pH. Nitrification rate also decreased as NH₄ ⁺‐N accumulated under acid soil conditions. Sodium acetate extractable P was positively linearly correlated (R²= 0.87) with soil pH over the entire pH range evaluated. Potassium chloride extractable Al was less than 1.3 mg kg^‐1of soil at pH values higher than 4.4. Consequently, potential Al toxicity problems in these soils are minimal. Extractable Mn increased with decreasing soil pH. Soil CEC, extractable Mg, and extractable K all decreased with increasing soil pH from 3.3 to 7.0. Extractable Ca levels were largely unaffected by changing soil pH. It is likely that the availability of N and P would be the most adversely affected parameters by soil acidification     

Rapid changes in carbon and phosphorus after rewetting of dry soil

Drying–rewetting (DRW) cycles are important for soil organic matter turnover; however, few studies have considered the short-term effects on nutrient availability. The pulses in soil respiration, extractable C, P and N pools were quantified after a single DRW cycle (ten sampling times over 49 h). Soil was pre-incubated with or without glucose (2.5 g kg⁻¹) for 10 days to induce differences in the size and activity of the microflora and then either subjected to a single DRW cycle (7-day drying period) or kept constantly moist. A resin extractable P (P_resin) method was used and compared to extraction of dissolved organic (DOP) and inorganic P (DIP) with a salt solution. The pulse in soil respiration, extractable organic C (EOC), P_resin, DOP and DIP was immediate and greatest in the first 2 h. The P_resin pulse was two to three times that measured by solution extraction (DIP). Also, P_resin quantified temporal changes in P not apparent in DIP, indicating the advantage of anion-exchange membranes in quantifying short-term changes in P availability. The P_resin pulse was smaller in the soil incubated with glucose showing that P pulses will be quantitatively smaller in a soil with an active microbial biomass. In contrast to P, pre-incubation with glucose did not alter EOC concentration or the pulse in EOC after rewetting. The P_resin pulse had disappeared by 49 h after DRW despite continued elevated rates of respiration. The sustained increase in DIP following DRW may have implications for plant availability or environmental losses.     

Effects of tillage and nitrogen management on soil chemical and physical properties after 23 years of continuous sorghum

Long-term tillage and nitrogen (N) management practices can have a profound impact on soil properties and nutrient availability. A great deal of research evaluating tillage and N applications on soil chemical properties has been conducted with continuous corn (Zea Mays L.) throughout the Midwest, but not on continuous grain sorghum (Sorghum bicolor (L.) Moench). The objective of this experiment was to examine the long-term effects of tillage and nitrogen applications on soil physical and chemical properties at different depths after 23 years of continuous sorghum under no-till (NT) and conventional till (CT) (fall chisel-field cultivation prior to planting) systems. Ammonium nitrate (AN), urea, and a slow release form of urea were surface broadcast at rates of 34, 67, and 135 kg N ha⁻¹. Soil samples were taken to a depth of 15 cm and separated into 2.5 cm increments. As a result of lime applied to the soil surface, soil pH in the NT and CT plots decreased with depth, ranging from 6.9 to 5.7 in the NT plots and from 6.5 to 5.9 in the CT plots. Bray-1 extractable P and NH₄OAc extractable K was 20 and 49 mg kg⁻¹ higher, respectively, in the surface 2.5 cm of NT compared to CT. Extractable Ca was not greatly influenced by tillage but extractable Mg was higher for CT compared to NT below 2.5 cm. Organic carbon (OC) under NT was significantly higher in the surface 7.5 cm of soil compared to CT. Averaged across N rates, NT had 2.7 Mg ha⁻¹ more C than CT in the surface 7.5 cm of soil. Bulk density (Δ_b) of the CT was lower at 1.07 g cm⁻³ while Δ_b of NT plots was 1.13 g cm⁻³. This study demonstrated the effect tillage has on the distribution and concentration of certain chemical soil properties.     

The effect of Ferralsol mineralogy on the distribution of organic C across aggregate size fractions under native vegetation and no‐tillage agriculture

No‐tillage management can increase soil surface layer organic C (OC) levels compared with conventional tillage. The mechanisms underlying this increase in highly weathered tropical soils, such as Ferralsols, are not well established. The objective of this study was therefore to evaluate the influence of mineralogy on aggregation and the apportionment of OC across aggregate size fractions in a Brazilian Ferralsol under native vegetation (NV) and no‐tillage management for 10 (NT10) or 20 (NT20) yrs. Under native vegetation, soil OC generally increased with increasing aggregate size while, in response to changing management, soil OC increased in the order NT10 (8.8 g/kg) < NT20 (12.7 g/kg) < NV (19.1 g/kg). There were no significant differences in the mineralogy of the clay size fractions among the three treatments, with the notable exception of the CBD‐extractable Fe oxide fraction (Fe_CBD). The Fe_CBD fraction comprises various pedogenic Fe(hydr)oxides and increased from NT10 (33.9 g/kg) to NT20 (64.2 g/kg). The OC/Fe_CBD mass ratio within aggregates increased in the order NT10 <  NT20 <  NV while R² values for OC and Fe_CBD occurrence follow this same trend, with the NT10 soil showing a weaker correlation (R² = 0.178) compared with the NV soil (R² = 0.533). We propose that formation of organo‐Fe(III) oxide associations is promoted with implementation of NT management and the consequent reduction in macroaggregate turnover. The development of the OC‐Fe(III) oxide associations and their evolution over time within aggregates to more thermodynamically stable entities will strongly influence the long‐term preservation of soil OC.     

Improvement of the NH2OH-HCl-HOAc method for extracting manganese and iron oxides in Japanese Andisols and other soil types in Japan

Abstract

We evaluated the validity of Tessier’s method as applied to the extraction of manganese (Mn) and iron (Fe) oxides in Japanese Andisols and other soil types in Japan. Using the original Tessier’s extractant mixture, 0.04 mol L^?1 hydroxylamine hydrochloride in 25% acetic acid (0.04 mol L^–1 NH₂OH-HCl in 25% HOAc), we found that substantial amounts of short-range-ordered Fe oxides were not extracted from allophanic Andisol samples and that considerable amounts of total Fe oxides were not extracted from all soil types. Relatively high extraction pH and large amounts of short-range-ordered Fe oxides in the Andisol samples might be responsible for incomplete extraction. Stoichiometric calculation indicated that the concentration of NH₂OH-HCl might be insufficient for complete extraction of Fe oxides. The extracted amounts of Mn and Fe increased with increasing concentration of NH₂OH-HCl in the extractant, and most of the Mn and Fe oxides in the soil samples, including samples with as much as 5.6% Fe, were extracted with 0.6 mol L^–1 NH₂OH–HCl in 25% HOAc. As judged from the simultaneous dissolution of aluminum (Al) and silicon (Si) minerals, extraction selectivity of Fe oxides with 0.6 mol L^–1 NH₂OH-HCl in 25% HOAc was comparable to that of the original Tessier’s method and better than that of a modified Community Bureau of Reference (BCR) sequential extraction procedure or a method using an extractant consisting of a mixture of oxalate and ascorbate, especially for Andisol samples.     

Different response of silicate fertilizer having electron acceptors on methane emission in rice paddy soil under green manuring

Cultivation of green manure plants during the fallow season in rice paddy soil has been strongly recommended to improve soil properties. However, green manuring may impact greenhouse gas emission, methane (hereafter, CH₄) in particular, under the flooded rice cultivation and thus, application of chemical amendments being electron acceptors can be an effective mitigation strategy to reduce CH₄ emissions in irrigated rice (Oryza sativa L.) field amended with green manure. To investigate the effect of iron (Fe) slag silicate fertilizer (hereafter, silicate fertilizer), which was effective in reducing CH₄ emission and increasing rice productivity, in green manure-amended paddy soil, the aboveground biomass of Chinese milk vetch (hereafter, vetch) was added at rates of 0, 10, 20, and 40 Mg (fresh weight) ha⁻¹ before the application of silicate fertilizer, which was added at rates of 0 and 2.3 Mg ha⁻¹. Silicate fertilization reduced the seasonal CH₄ flux by ca. 14.5% and increased rice yield by ca. 15.7% in the control (no vetch application) treatment. However, CH₄ production was increased by silicate fertilization in vetch-treated soil particularly at the initial rice growing stage, which was probably due to the enhanced decomposition of added organic matters by the silicate liming effect. In conclusion, silicate fertilization is not effective in reducing CH₄ production in green manure-amended rice paddy soils and its use should be properly controlled.     

A critical assessment of soil amendments (slaked lime/acidic fertilizer) for the phytomanagement of moderately contaminated shooting range soils

Purpose  

The effects of the addition of an acidic fertilizer solution and/or slaked lime (5.5 g Ca(OH)₂ kg⁻¹) on a slightly acidic shooting range soil (pH 6.1, % organic carbon 5.4) with moderate metal (e.g., 620 mg kg⁻¹ Pb) and metalloid (17 mg kg⁻¹ Sb) concentrations on metal and Sb solubility and plant accumulation were investigated.     

Behavior of soil boron and boron uptake by M.26 apple rootstock as affected by application of different forms and nitrogen rates

Abstract

The changes in availability and uptake of boron (B) by M.26 apple rootstocks as affected by applications of different forms and rates of nitrogen (N) were examined. The study was carried out in a greenhouse using soil with low contents of organic matter, clay, calcium carbonate, NH₄‐oxalate soluble aluminum (Al) and iron (Fe), NH₂OH·HCl extractable manganese (Mn), poor cation exchange capacity and low pH. Soil N application was in the form of urea, calcium nitrate, ammonium sulphate, or ammonium nitrate at rates of 0, 17, 34, and 51 mg N kg^?1. After 1, 3, and 5 days of N application, soil B fractions were determined: B in soil solution, B specifically and non‐specifically adsorbed on soil surfaces, B occluded in Mn oxyhydroxides, and B occluded in crystalline Al and Fe oxides. The results showed that N as calcium nitrate and ammonium nitrate increased B both in soil solution and non‐specifically adsorbed on soil surface and decreased B concentration on Al and Fe oxides. This indicates that N‐NO₃ inhibited B sorption on Fe and Al oxides. Maximum B desorption from Fe and Al oxides was obtained within one day after N‐NO₃ was supplied. Nitrogen application as calcium nitrate and ammonium nitrate increased availability and uptake of B by plant roots. Thus, it was concluded that apple trees planted on coarse‐textured soils where risk of B deficiency is high, calcium nitrate or ammonium nitrates would be appropriately to apply to keep B more available.     

Silicon,aluminum, and oxalic acid interactions in two California forest soils

Abstract

The release of solid‐phase soil aluminum (Al) from two soils was studied under acidic conditions and also in the presence of monosilicic acid. The soils support mixed‐conifer forests in the mid‐elevation Western Sierra Nevada in northern California, but differ in their state of development and mineralogy as shown by Al, iron (Fe), and silicon (Si) concentrations. The pyrophosphate‐extractable Al (Al_p) pool, which was a main source of released Al, decreased after a two‐month leaching with nitric (HNO₃) or oxalic (HO₂C‐CO₂H) acids. Addition of monosilicic acid (SiO₂.XH₂O) to the acid extractants resulted in a further decrease of Al. Solution monosilicic acid was removed from solution by sorption on Fe oxides/hydroxides in the soil with the higher dithionite‐extractable Fe pool. In the less developed soil with lower pedogenic Fe, the formation of short‐range‐ordered aluminosilicates, even in the presence of a strong Al chelator, was responsible for the removal of a portion of the monosilicic acid from solution. Pedogenic Fe inhibited the formation of short‐range‐ordered aluminosilicates more than the presence of a strong Al chelator. Both the solution phase and surface reactions are important in the pedogenic formation of alumino‐silicate minerals.     

Reductive dissolution of crystalline and amorphous Fe(III) oxides by microorganisms in submerged soil

Summary Reduction of Fe(III) of amorphous and crystalline Fe(III) oxides to Fe(II) in flooded soils was studied using ⁵⁹Fe(OH)₃ and ⁵⁹Fe₂O₃. The results indicated that Fe(III) in the amorphous oxide was readily amenable to microbial reduction in anaerobic soil condition whereas Fe(III) in the crystalline oxide was not. Following soil submergence, the native as well as the applied crystalline Fe(III) oxides were rapidly converted into the amorphous form. The transformation of the crystalline oxides to the amorphous form appears to be a prerequisite for the reduction of Fe(III) of the oxide. This transformation, probably through hydration, is also mediated by microorganisms.     

Wetland conversion to beef cattle pasture changes in soil properties

Background and Objective  Largely influenced by the passage of the Swamp Land Act of 1849, many wetlands have been lost in the coastal plain region of southeastern United States primarily as a result of drainage to convert land for agriculture. While further wetland conversion or loss is universally acknowledged, the process continues with little public recognition of the causes or consequences. This study examined changes in soil carbon, pH, and Mehlich extractable nutrients in soils following conversion of wetland to beef cattle pasture. Methods  To better understand the chemical response of soils during wetland conversion to beef cattle pasture, soil samples were collected from the converted beef cattle pastures and from the adjoining reference wetland. Soil samples were collected from eleven sites in the beef cattle pasture, and from four in the adjoining reference wetland. Data that were collected from the reference wetland sites were used as the reference/baseline data to detect potential changes in soil properties associated with the conversion of wetlands to beef cattle pastures from 1940 to 2002. Results and Discussion  Compared with the adjoining reference wetland, the beef cattle pasture soils in 2002, 62 years after being drained, exhibited: (1) a decrease in organic carbon, TOC (-172.3 g kg^-1), nitrogen, TN (-10.1 g kg^-1), water soluble phosphorus, WSP (-5.1mg kg^-1), and potassium, K (-0.7 mg kg^-1); (2) an increase in soil pH (+1.8 pH unit), calcium, Ca (+88.4 mg kg^-1), magnesium, Mg (+7.5 mg kgc), manganese, Mn (+0.3 mg kg^-1), and iron, Fe (+6.9 mg kg^-1); and (3) no significant changes in sodium (Na), zinc (Zn), copper (Cu), and aluminum (Al). In 2002, the amount of TOC and the concentration of soil organic matter (OM) in pasture fields were significantly lower than the concentration in the reference wetland with average values of 7.8 ± 8 g kg^-1 and 36 ± 26 g kg^-1 and 180.1 ± 188 g kg^-1 and 257 ± 168 g kg^-1, respectively. It appeared that conversion of wetlands was proceeding toward a soil condition/composition like that of mineral soils. Conclusion and Outlook  Overall, conversion of wetland had significant effects on soil carbon, pH, nitrogen, phosphorus, and extractable nutrients. Results of our study have shown a decrease in TOC, TN, WSP, and K and an increase in soil pH, Ca, Mg, Mn, and Fe. These results are important in establishing useful baseline information on soil properties in pasture and adjoining reference wetland prior to restoring and converting pasture back to its original wetland conditions as a major part of the restoration effort being underway.     

Element fractionation in soil from urban-industrialized areas using sequential extraction

Background Goal and Scope  

The application of solid-liquid extraction is proposed to assess extractable fractions of components in soil. The application of a several step scheme could give a lot of information about mobility of metals associated with specific solid phases, especially after separation of top and bottom layers of studied soil. In this study, it was aimed to take into solution metal fractions of major (Ca, Mg, Mn, Fe) and trace elements (Cr, Co, Cu, Zn, As, Cd, Pb) from soil collected in urban areas. The fractions were defined by using chemical extraction operationally. The extraction behavior of studied elements in a six-step sequential extraction procedure is discussed with respect to the properties of the reagents used.     

Effect of elemental sulphur and sulphur containing waste in a calcareous soil in Turkey

The effect of elemental sulphur (S) and S containing waste applications on soil pH treated with 0–2,000 kg ha^‐l elemental S, and 0–100 tons ha‐¹ of waste was determined in the field and the pots. Sorghum (Sorghum bicolor L.) was grown in a Lithic Xerorthent soil which was taken from where the field experiment was conducted in pots receiving 5 kg soil. Plants were harvested 20 weeks after planting or 30 weeks after the applications for determination of dry matter yield and phosphorus (P), iron (Fe), zinc (Zn), manganese (Mn), and copper (Cu) uptake by shoots. EC, NaHCO₃‐extractable P, and DTPA‐extractable Fe, Zn, Mn, Cu also were measured in pot soil at the 5th, 10th, and 30th weeks. All treatments led to a decrease in soil pH though pH tended to increase again during course of time in both field and pot experiments. The both elemental S and waste applications in pot experiment caused an increase in dry matter yield and P, Fe, zinc (Zn), Mn and Cu uptake (mg pot^‐1) by shoots in sorghum plant. There was also an increase in EC of soil due to both applications of S. The concentration of available P extracted by NaHCO₃ in the pot soil, though not significantly different, was slightly higher compared with the control. Waste applications increased DTPA‐extractable Fe content of the soil, DTPA‐extractable Mn and DTPA‐extractable Cu. DTPA‐extractable Zn content, however, was reduced by the same applications.     

Effects of climatic factors and soil management on the methane flux in soils from annual and perennial energy crops

Methane flux rates were measured on a loamy sand soil within perennial and annual energy crops in northeast Germany. The study was performed in closed chambers between 2003 and 2005 with four measurements per week. A mixed linear model including the fixed effects of year, rotation period, crop and fertilisation was applied to determine the influence of climatic factors and soil management on the CH₄ flux. Soil water content and air temperature were added as co-variables. With the exception of air temperature, all fixed effects and the co-variable soil water content influenced the CH₄ flux. The soil of annual crops consumed 6.1 μg CH₄ m⁻² h⁻¹, significantly more than the soil of perennial crops with 4.3 μg CH₄ m⁻² h⁻¹. It is suggested that soil water content plays the key role in CH₄ flux between pedosphere and atmosphere. In the range of water contents between 5% and 15%, our model describes that a soil water content increase of 1% induces a net emission of 0.375 μg CH₄ m⁻² h⁻¹. As the soil of the experimental field was well-drained and aerobic, it represented a net sink for CH₄ throughout the study period.     

Relationships between soil pH and microbial properties in a UK arable soil

Effects of changing pH along a natural continuous gradient of a UK silty-loam soil were investigated. The site was a 200 m soil transect of the Hoosfield acid strip (Rothamsted Research, UK) which has grown continuous barley for more than 100 years. This experiment provides a remarkably uniform soil pH gradient, ranging from about pH 8.3 to 3.7. Soil total and organic C and the ratio: (soil organic C)/(soil total N) decreased due to decreasing plant C inputs as the soil pH declined. As expected, the CaCO₃ concentration was greatest at very high pH values (pH > 7.5). In contrast, extractable Al concentrations increased linearly (R² = 0.94, p < 0.001) from below about pH 5.4, while extractable Mn concentrations were largest at pH 4.4 and decreased at lower pHs. Biomass C and biomass ninhydrin-N were greatest above pH 7. There were statistically significant relationships between soil pH and biomass C (R² = 0.80, p < 0.001), biomass ninhydrin-N (R² = 0.90, p < 0.001), organic C (R² = 0.83, p < 0.001) and total N (R² = 0.83, p < 0.001), confirming the importance of soil organic matter and pH in stimulating microbial biomass growth. Soil CO₂ evolution increased as pH increased (R² = 0.97, p < 0.001). In contrast, the respiratory quotient (qCO₂) had the greatest values at either end of the pH range. This is almost certainly a response to stress caused by the low p. At the highest pH, both abiotic (from CaCO₃) and biotic Co₂ will be involved so the effects of high pH on biomass activity are confounded. Microbial biomass and microbial activity tended to stabilise at pH values between about 5 and 7 because the differences in organic C, total N and Al concentrations within this pH range were small. This work has established clear relationships between microbial biomass and microbial activity over an extremely wide soil pH range and within a single soil type. In contrast, most other studies have used soils of both different pH and soil type to make similar comparisons. In the latter case, the effects of soil pH on microbial properties are confounded with effects of different soil types, vegetation cover and local climatic conditions.     

Solubility of soil phosphorus as influenced by urea

The objective of this study was to investigate possible ways of mobilizing residual fertilizer P as a result of local pH elevation caused by urea hydrolysis. The response of water-soluble P (P_w) and dissolved organic C (DOC) to urea hydrolysis was monitored in three cultivated soils and at two P levels for up to 127–135 d and compared with corresponding changes in soils limed with Ca(OH)₂. Hydrolysis of urea was complete in 8–15d during which soil pH increased by 1–1.5 units at the maximum. Subsequently, the pH decreased to or below the original level owing to nitrification. Mobilization of soil P was enhanced substantially in parallel with the increase in pH, the peak P_w occurring simultaneously with the highest pH value. In all urea-treated soils, P_w remained at an elevated level for at least 60d. As compared to urea, elevation of soil pH with Ca(OH)₂ had only a minor and inconsistent influence on P_w. In mobilization of soil P, the urea-induced increase in pH and a simultaneous production of NH₄⁺ ions proved to be superior to liming with Ca(OH)₂. It was hypothesized that when an acid soil is amended with urea, phosphate is first displaced by OH^? ions, resulting in elevated solution P concentrations. A simultaneous dissolution of organic matter contributes to the persistence of high P concentration by competition for sorption sites on Fe and Al oxides, and thus retards the resorption of P.