Soil Inorganic Phosphorus Fractionation and Availability under Greenhouse Subsurface Irrigation

Inorganic phosphorus (P) fractions and their availability under subsurface irrigation were investigated in a greenhouse planted for 5 years with tomato. Irrigation was applied when soil water conditions reached the predefined maximum allowable depletion (MAD) for different treatments, e.g., ?10 kPa, ?16 kPa, ?25 kPa, ?40 kPa, and ?63 kPa. Concentrations of five inorganic P fractions, which include of soluble / loosely bound P, aluminum (Al) P, iron (Fe) P, calcium (Ca) P, and occluded P, were obtained by following a sequential chemical fractionation procedure. Results showed that the effect of subsurface irrigation and schedules on inorganic P fractions was more pronounced in topsoil layers than in deep soils. The concentrations of soluble / loosely bound P, Al P, and Fe P generally decreased with soil depth, having the largest values at the depths of 0–10 cm and 10–20 cm. In all the irrigation treatments, Al P and Fe P were the dominant fractions at the depths of 0–10 cm, 10–20 cm, and 20–30 cm, whereas Ca P and occluded P were most predominant at the depths of 30–40 cm and 40–60 cm. Soluble or loosely bound P, Al P, and Fe P were the main sources contributing to plant-available P, whereas Fe P and Al P were the two most important sources for contribution to plant-available P. Frequent irrigation with small amounts of water (e.g., irrigation with MAD of ?16 kPa and ?25 kPa) yielded larger concentrations of soluble / loosely bound P, Al P, and Fe P, which are the main sources of plant-available P. However, infrequent irrigation with larger amounts of water in each irrigation event led to greater concentrations of Ca P and occluded P, which are relatively less available to plants.     

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.     

Availability of soil boron fractions to M.26 apple rootstock

The availability of various boron (B) fractions in soil to M.26 apple (Malus spp.) rootstock was examined. The study was carried out in a greenhouse on soils with diverse chemical and physical properties. The following B fractions were determined: (i) B in soil solution, (ii) B non‐specifically adsorbed on soil surface, (iii) B specifically adsorbed on soil colloid surfaces, (iv) B occluded in Mn oxyhydroxides, (v) B occluded in noncrystalline aluminum (Al) and iron (Fe) oxides, (vi) B occluded in crystalline Al and Fe oxides, (vii) B fixed with soil silicates, and (viii) total soil B. In the studied soils there were: 0.07–0.17 mg kg^‐1 B in soil solution, 0.01–0.03 mg kg^‐1 B non‐specifically adsorbed on soil surface, 0.04–0.08 mg kg^‐1 B specifically adsorbed on soil colloid surfaces, 0.28–0.67 mg kg^‐1 B occluded in manganese (Mn) oxides, 4.03–17.22 mg kg^‐1 B occluded in noncrystalline Al and Fe oxides, 8.93–50.62 mg kg^‐1 B occluded in crystalline Al and Fe oxides, 12.2–42.5 mg kg^‐1 B fixed with soil silicate, and 52.9–82.2 mg kg^‐1 total B. Simple correlation analysis showed positive correlation between B contents in M.26 apple rootstocks and amounts of B in soil solution (r=0.77), B non‐specifically adsorbed on soil colloid surfaces (r=0.65), B specifically adsorbed on soil surface (r=0.76) and B occluded in Mn oxyhydroxides (r=0.77). No relation was found between plant B contents and amounts of B occluded in non‐crystalline and crystalline Al and Fe oxides, B fixed with soil silicates and total B. The results indicated that extraction of B by 0.1 M NH₂OH HCl solution adequately represented amounts of B in soil solution, B non‐specifically and specifically adsorbed on soil compound surfaces and B occluded in Mn oxyhydroxides to assess availability of B to apple trees.     

Mycorrhizal (Rhizophagus Intraradices) Symbiosis and Fe and Zn Availability in Calcareous Soil

Greenhouse experiment was conducted to assess the iron (Fe) and zinc (Zn) fractionation patterns in soils of arbuscular mycorrhizal (AM) fungus-inoculated and uninoculated maize plants fertilized with varying levels of Fe and Zn. Soil samples were collected for Fe and Zn fractions and available Fe, Zn and phosphorus (P) contents besides organic and biomass carbon (BMC), soil enzymes and glomalin. Major portion of Fe and Zn fractionations was found to occur in the residual form. Mycorrhizal symbiosis increased the organically bound forms of Fe and Zn while reducing the crystalline oxide, residual Fe and Zn fractions, indicating the transformation of unavailable forms into available forms. Soil enzymes, viz. dehydrogenase and acid phosphatase activities in M+ soils, were significantly higher than M? soil consistently. Overall, the data suggest that mycorrhizal symbiosis enhanced the availability of Fe and Zn as a result of preferential fractionation and biochemical changes that may alleviate micronutrient deficiencies in calcareous soil.

Abbreviations: AM: arbuscular mycorrhiza; Fe: Iron; Zn: Zinc; P: Phosphorous; Amox-Zn: amorphous oxide bound zinc; Cryox-Zn: crystalline oxide bound zinc; DAS: days after sowing; DTPA: diethylene Triamine Penta Acetic Acid; MnO₂-Zn: manganese oxide bound zinc; OC-Zn: organically bound zinc; WSEX: water soluble plus exchangeable zinc; MnO₂ Fe: manganese oxide bound iron; OC-Fe: Organically bound iron; WSEX Fe: water soluble plus exchangeable iron.     

Extractability and Transformation of Copper and Zinc Added to Tropical Savanna Soil under Long-Term Pasture

The extractability and slow reactions of copper (Cu) and zinc (Zn) in a weathered savanna soil under Brachiaria decumbens, Digitaria smutsii, and Stylosanthes guianensis pastures were determined in a laboratory incubation study using a sequential extraction to remove operationally defined fractions of the metals, consisting of exchangeable, organically bound, precipitate [occluded in aluminum (Al) and iron (Fe) oxides], and residual metal fractions. The soils from the pasture fields were spiked with 100 mg Cu kg^–1 soil and 200 mg Zn kg^–1 soil for 24 weeks. Copper and Zn extractable with 1 N potassium nitrate (KNO₃) solution decreased exponentially with time but reached a steady state after 2–3 weeks. The concentrations of Cu and Zn exchangeable with potassium (K) were greater in the Digitaria smutsii field soil than Brachiaria decumbens and Stylosanthes guianensis field soils. The exchangeability of added Cu and Zn (indexed Mⁿ⁺ _(exch)) with time was described by a simple exponential decay equation: Mⁿ⁺ _(exch) = αe^βt, where α is a constant, β is a coefficient that defines the rate of transformation of added Cu and Zn from the exchangeable to nonexchangeable pools, and t is time. The β values for Cu (0.040–0.076 mg kg^–1 d^–1) were almost 10 times greater than those of Zn (0.005–0.007 mg kg^–1 d^–1). Sequential extraction of added Cu and Zn indicated that between 26 and 30% of the total Cu and between 19 and 30% of the total Zn were associated with organic matter. Similarly, between 35 and 38% of total Cu and between 47 and 60% of total Zn were associated with Fe, Al, and manganese (Mn) oxides. The differential capacity of the pasture fields to transform added Cu and Zn from exchangeable and labile form to nonlabile and nonexchangeable form appears to be governed by organic matter (OM), pH, and active Fe ratio in the pasture field soils.     

Impact of boron fertilization on boron fractions at different crop growth stages in cauliflower_cowpea_okra sequence in an inceptisols of North East India

Abstract

A field experiment was conducted at Horticultural Experimental Farm, Assam Agricultural University, Jorhat during the year 2015–17 to assess the impact of boron fertilization on dynamics of boron fractions in soil and crop yields in cauliflower–cowpea–okra cropping sequence. Five levels of boron (0, 0.5, 1.0, 1.5 and 2.0?kg ha^?1) along with the recommended dose of NPK fertilizer were applied in soil in cauliflower once in each 2 years (2015–17) of experimentation to assess the direct effect of boron fertilization, while cowpea and okra were grown as a suceeding test crop to study the residual effects of boron fertilization in the cropping sequence. Among the different levels of boron, the highest content of all the boron fractions in soil was recorded at rate of 2?kg B ha^?1 at different crop growth stages for all the three crops. Progressive decrease in content of all the boron fractions with crop ageing was noticed. The content of different boron fractions in soil follows the order readily soluble boron (RSB)<oxide bound boron (OXB)<organic bound boron (ORBB)<specifically adsorbed boron (SAB) <residual boron, respectively. The boron level of 2?kg B ha^?1 was found to prominent in increasing the yield in all the crops. In respect of contributions of different boron fractions to yield of crops, oxide bound boron(2.10) was found to be the highest contributor of cauliflower yield, while the residual boron (1.10), contributed the highest to cowpea yield and organic bound boron fraction (1.24) was found to be most prominent contributor of boron in leveraging okra yield.     

Chemical Fractions of Mn in Acidic Soils and Selection of Suitable Soil Extractants for Assessing Mn Availability to Maize (Zea Mays L.)

Twenty surface (0–15 cm) samples of acidic soils were analyzed for water soluble (WS), exchangeable (EX), lead displaceable (Pb-disp.), acid soluble (AS), manganese (Mn) oxide occluded (MnOX), organically bound (OB), amorphous Fe oxide occluded (AFeOX), crystalline iron (Fe) oxide occluded (CFeOX) and residual (RES) fractions of Mn, and also for extractable Mn in some common soil extractants: (diethylenetriaminepentaacetic acid (DTPA) (pH 7.3), DTPA (pH 5.3), AB-DTPA (pH 7.6), Mehlich-3 (pH 2.0), Modified Olsen, 0.005 M calcium chloride (CaCl₂), 1 M magnesium chloride (MgCl₂) and ion exchange resins. The WS-Mn fraction showed a significant and positive correlation with Mn extractable in DTPA (pH 5.3) and AB-DTPA (pH 7.6), while both WS-Mn and EX-Mn fractions correlated significantly and positively with Mn concentration and uptake by maize plants grown in these soils. The AB-DTPA (pH 7.6) and DTPA (pH 5.3) appeared suitable to assess the availability of Mn in acidic soils.     

Fractionation and colorimetric determination of boron in soils

We attempted to modify and evaluate existing sequential fractionation schemes for B involving the use of chemicals, which subsequently do not interfere with the measurement of B by colorimetry. Also evaluated was the contribution of various soil B fractions to the amount of B extracted by hot CaCl₂, CaCl₂‐mannitol, salicylic acid, ammonium acetate, HCl, and tartaric acid. For this purpose, 17 soils with diverse properties were used. The extraction scheme proposed here partitioned B into five pools, (i) readily soluble, (ii) specifically adsorbed, (iii) oxide bound, (iv) organically bound, and (v) residual boron, respectively extracted with 0.01 M CaCl₂, 0.05 M KH₂PO₄, 0.175 M NH4‐oxalate (pH 3.25), 0.5 M NaOH, and HF + H₂SO₄ + HClO₄. The procedure of elimination of color from extracts of oxide bound, organically bound, and residual B fractions was also evolved. Relationships of individual B fractions with physicochemical properties of the experimental soils confirmed the general validity of the proposed fractionation scheme. The relationships of different B fractions with extractable B in soils suggest that hot CaCl₂ and salicylic acid may be better extractants for available B in soils.     

Distribution of Boron in Different Fractions in Some Alkaline Calcareous Soils

Distribution of boron (B) in different fractions is still not well defined when it is applied in B-deficient alkaline calcareous soil and after harvesting of the sown crop. In the present greenhouse experiment with green gram crop, three B-deficient soils with calcium carbonate contents of 0.8 (S I), 2.1 (S II), and 4.6 (S III) percent were collected from different sites in Ludhiana and Bhatinda Districts, Punjab, India. The treatments composed of five levels of soil-applied B (0, 0.5, 0.75, 1.0, and 1.5 mg B kg^?1) soil and the experiment was laid out in Completely Randomized Design (CRD) factorial design with three replications. Mean readily soluble, specifically adsorbed, and oxide-bound B fractions got increased significantly with increase in B applications. Distribution of readily soluble B was more in low calcareous soil than in high calcareous soil. Mean values of specifically adsorbed, oxide-bound, residual, and total B were significantly more in high calcareous soils as compared to low calcareous soils. At maturity, specifically adsorbed B converted into other fractions to maintain equilibrium in soil solution. Organically bound B was greater than the oxide-bound B fraction. Among all fractions, residual fraction accounted for the major portion of the total B. Available B was negatively and significantly correlated with calcium carbonate (CaCO₃) content of soil (r = ?0.99*). At the same time, specifically bound B was also negatively and significantly correlated with readily soluble B (r = ?0.99*) whereas organically bound B was positively correlated with organic carbon content of soil (r = ?0.99*).     

Impact of Soil Sorption Characteristics and Bedrock Composition on Phosphorus Concentrations in two Bohemian Forest Lakes

Phosphate (PO₄-P) sorption characteristics of soils and bedrock composition were determined in catchments of two mountain lakes, Ple?né Lake (PL) and ?ertovo Lake (CT), situated in the Bohemian Forest (Czech Republic). The aim was to explain higher terrestrial P export to mesotrophic PL compared to oligotrophic CT. Concentrations of Al and Fe oxides were the dominant parameters affecting soil ability to adsorb PO₄-P. Depending on concentrations of Al and Fe oxides, P sorption maxima varied from 9.7 to 70.5 mmol kg^?1 and from 7.4 to 121 mmol kg^?1 in organic and mineral soil horizons, respectively. The catchment weighted mean PO₄-P sorption capacity was 3.4 mol m^?2 and 11.9 mol m^?2 in the PL and CT soils, respectively. The higher PO₄-P sorption capacity in the CT catchment was predominantly associated with higher pools of soil and Fe oxides. The CT bedrock (mica schist) released one order of magnitude less P than the PL bedrock (granite) within a pH range of catchment soils (pH_CaCl2 of 2.5–4.5). The higher ability of PL bedrock to release P and the lower ability of PL soils to adsorb PO₄-P thus contributed to the higher terrestrial P loading of this lake.     

Influence of soil applied boron on yield of berseem (Trifolium alexandrium L.) and soil boron fractions in calcareous soils

A greenhouse experiment was conducted in North-west India to study the effect of soil applied boron on yield of berseem (Trifolium alexandrium L.) and soil boron fractions in boron deficient calcareous soils. Three soils with varying calcium carbonate content viz. 0.75% (Soil I), 2.6% (Soil II), and 5.7% (Soil III) were collected from different sites of Ludhiana, Bathinda, and Shri Muktsar Sahib districts, Punjab, India. The treatments consisted of six levels of soil applied boron viz. 0.5, 0.75, 1.0, 1.25, 1.5, and 2.0 mg B kg^?1 along with control. The green fodder yield and dry matter yield increased significantly at 0.75 mg B kg^?1 soil treatment level in the first cutting, while these were significant at 1.0 mg B kg^?1 soil treatment level in all soils at second, third, and fourth cuttings. Among all three calcareous soils, Soil I with lower calcium carbonate was the best soil in respect of mean yield in comparison to Soil II and Soil III. Combined effect of boron level and soils had significant effect on yield of berseem. There was a significant increase in mean dry root biomass at 1.0 mg B kg^?1 soil level over control and then remained non-significant with further high levels of soil applied boron. The mean dry root biomass decreased significantly for the soils having 0.75%, 2.6%, and 5.7% calcium carbonate levels. Readily soluble fraction is considered to be easily available fraction of B for plant uptake and consisted of 0.47–0.62% in Soil I, 0.31–0.43% in Soil II, and 0.24–0.34% in Soil III of the total boron. Among all B fractions, mean readily soluble, specifically adsorbed, and oxide-bound fractions got increased significantly with increase in B levels. Readily soluble and organically bound B fractions were more in Soil I as compared to Soil II and Soil III. Specifically adsorbed boron, oxide bound fraction, residual and total boron were more in Soil III in comparison to Soil I and Soil II. Among all fractions, residual fraction accounted for the major portion of the total B. It comprised of 92.71–93.90% in Soil I, 94.51–95.40% in Soil II, and 94.91–95.25% in Soil III of the total boron.     

Organic and Mineral Fertilization: Effects on Physical Characteristics and Boron Dynamic in an Agricultural Soil

Abstract

The mineral and organic fertilizations on lettuce (Lactuca sativa L.) cultivation were investigated to understand the correlations between soil physical and mechanical indexes and boron (B) dynamic (adsorption, desorption, fractions) in soil. The fertilization with compost (derived by wine‐producing residues) and integrated fertilization (compost plus ammonium nitrate) increased the soil workability, as do the extent of aggregation, the water retention, and the cation exchange of the soil. The physical (colloids index, Ic) and mechanical (shear resistance, τ) properties showed a significantly higher value in compost and integrated fertilization plots. The biomass application to the soil influences the sorption B behavior, which is related to the soil shear strength and the compaction susceptibility; the Langmuir maximum adsorption for B was positively related with plastic deformation (De) and dry bulk density (Db) and negatively related to water infiltration (Wi), τ, and compressibility index (Cs).

The B desorption was not modified by the variation on soil mechanical resistance; no correlation was found between B desorption index and physical–mechanical parameters of the soil. The B fractions, not readily available for plants, occluded in aluminium (Al) and iron (Fe) oxyhydroxides (Ox‐B) and organically bound (OM‐B), were negatively correlated with colloid index (Ic), Wi, τ, and moisture content (U), and were positively correlated with De, Db, and compressibility index (Cp, related to organic‐matter content of the soil).     

Transformations and Availability of Iron to Wheat as Influenced by Phosphorus and Manganese Fertilization in a Typic Haplustept Soil

An investigation was conducted using Typic Haplustept, sandy loam soil, to investigate the interactive effects of phosphorus (P) and manganese (Mn) fertilization on native iron (Fe) pools in soil and their availability to wheat (cv. PBW-343) crop. Phosphorus fertilization moved Fe from residual mineral fraction of Fe to manganese oxides (MnOX), organic matter (OM), amorphous (AMPOX), and crystalline (CRYOX) Fe and Al oxide fractions. However, Mn application decreased specifically adsorbed (SAD)–Fe and CRYOX–Fe but increased OM–Fe and mineral fraction of Fe. Available Fe in soil decreased as Olsen P and P:Mn ratio increased in the soil. Higher Olsen P (>60 mg P kg^?1soil) reduced mean Fe uptake by shoot. P content and P:Mn ratio in soil as well as in root and shoot were inversely related to Fe concentration in both the plant parts. The role of soil Fe associated with oxides and organic matter was found most notable in Fe nutrition of wheat.     

Soil boron status: impact of lime and fertilizers in an Indian long-term field experiment on a Typic Paleustalf

In Indian agriculture, nitrogen (N) and phosphorus (P) fertilizers are predominantly used by the farmers, often ignoring secondary and micronutrients. Significance of boron (B) in nutrient management studies has been increasingly underlined under intensive cropping systems particularly in acid soils. In order to understand the distribution of soil native B in different fractions and their contribution to plant B uptake as influenced by nutrient management, soil samples collected after wheat (2009–2010) from a long-term experiment (LTE) continuing since 1972–1973 on Typic Paleustalf of Ranchi were subjected to sequential fractionation of soil B. Treatments included N alone, NP, NPK, 150% of recommended NPK, NPK + farmyard manure (FYM), NPK + lime, and an unfertilized-control. Five soil B fractions were determined along with hot CaCl₂-extractable (available) B. Averaged across the treatments, the soil had low organic carbon (C), pH and cation exchange capacity (CEC), and high free sesquioxides. Total B content was 21.7 mg kg^?1. Among different B fractions, residual B was the major contributor to total B and other fractions collectively shared 7% of total B only. Application of N alone depleted readily soluble, specifically adsorbed and organically bound B bringing the contents even below unfertilized-control. Conjoint use of lime or FYM with NPK increased significantly these fractions, whereas a decrease in oxide bound B was noticed under these treatments. Available B was positively correlated with these fractions indicating their significance in controlling B availability in the soil. The study revealed that use of lime or FYM helped modifying the distribution of soil B in different fractions by way of changing soil pH and organic C content, resulting in enrichment of plant available pool. A drastically low available B content in different treatments receiving fertilizers alone, however, suggested the necessity of B fertilization at prescribed rates for maintaining soil B fertility as also high crop yields.     

Soil aluminum and iron fractions and their relationships with P immobilization and other soil properties in andisols of costa rica and panama

Abstract

The immobilization of P is a significant fertility limitation of Andisols in Central America. It is believed that soil Al and Fe fractions have an important influence on P availability. This study was conducted to obtain information on the various forms of Al and Fe in ten pedons derived from volcanic ash in Panama and Costa Rica. Correlations between these Al and Fe fractions and P immobilization were measured by different methods.

The Al and Fe fractions, extracted by acid ammonium oxalate, 4M KOH, sodium pyrophosphate and dithionite‐citrate, were determined, and the correlations between these fractions, P immobilization, and other soil properties made.

It was observed that oxalate extractable Al correlated significantly with P immobilization, which had values of over 85% by the New Zealand method and 96% by the isotherm method. The Al concentration corresponding to this immobilization was over 2%. The difference between oxalate extractable Al and pyrophosphate extractable Al (inorganic Al fraction) correlated with P immobilization also. The pyrophosphate extractable Al fraction had the lowest concentrations and did not correlate with P immobilization. The NaF‐pH and dithionite‐citrate extractable Al correlated significantly with P immobilization.

Oxalate extractable Fe correlated with the P retained by the isotherm method, but dithionite‐citrate extractable Fe was negatively correlation with P immobilized. No correlations were found between the pyrophosphate extractable Fe and other soil properties.     

Availability of Organic and Inorganic Phosphorus Fractions to Wheat in Toposequences of Calcareous Soils

Abstract

Information on the availability of different soil phosphorus (P) forms is useful for crop production. Phosphorus contents of 12 Iranian calcareous soils from upper‐, mid‐, and lower‐slope positions of two arid and two semiarid toposequences were fractionated to various organic and inorganic pools, and correlations of the P fractions with wheat responses were investigated. Among the inorganic P (IP) fractions, apatite type (Ca₁₀‐P) and dicalcium phosphate equivalents (Ca₂‐P) possessed the highest and the lowest amounts of P reserve in the soils, respectively. On average, about 20% of the total P was found in organic form (OP), of which 32% was labile (LOP), 51% was moderately labile (MLOP), and 17% was nonlabile (NLOP). The amounts of the soil P fractions were considerably influenced by the positions of the soils on the landscapes. The maximum contents of soil IP, Ca₂‐P, Fe‐P (iron‐bound P), and Ca₁₀‐P were observed in the lower‐slope positions. The amount of soil available [0.5 M sodium bicarbonate (NaHCO₃) extractable] P was significantly correlated with Ca₂P (r=0.895), Fe‐P (r=0.760), and Occl‐P (iron‐occluded P) (r=0.897). Direct correlation studies, however, showed that wheat shoot dry‐matter yield (DMY) was significantly affected by the amounts of Ca₂‐P, Fe‐P, OP, LOP, and MLOP fractions both at early (4 weeks) and late (10 weeks) stages of growth. All organic and inorganic P fractions, except Al‐P (aluminum‐bound P), Ca₈‐P (octacalcium phosphate equivalents), and NLOP, also showed significant relations to the amount and/or concentration of P in wheat tissues at 4 and 10 weeks after sowing. Among the measured soil properties, the amount of organic carbon was the most affecting factor on the size of the P fractions.     

Assessment of zinc availability to rice in mollisols of North India

Abstract

The objectives of this study were to (1) characterize zinc (Zn) fractions and their relation to Zn extracted with mixed‐bed ion exchange resin capsules and (2) assess the relationships between the latter and Zn uptake by rice in 12 Mollisols from North India. The Resin Adsorption Quantity (RAQ) of Zn was measured after 1 and 14 days of anaerobic incubation. Six organic and inorganic Zn fractions were determined on anaerobic soil. Zinc uptake by rice was studied in a greenhouse experiment. Soil Zn fractions under reduced conditions followed the order residual Zn (80%)>carbonates and amorphous oxides bound Zn (12%)>weakly organically bound Zn (3%)>crystalline oxides bound Zn (2%)>strongly organically bound Zn (2%)>water soluble + exchangeable Zn (1%). RAQ‐Zn was best correlated with Zn bound to carbonates and amorphous oxides. Due to negative interactions between bicarbonate and Zn uptake, correlations between relative dry matter yield or total Zn uptake and the different Zn fractions, DTPA‐Zn measured on dry soil, or RAQ Zn were not significant. Adjusting soil test values according to soil pH improved the prediction of relative dry matter yield, but further studies are required to determine whether the resin capsule can be used as a soil test for Zn in calcareous soils.     

Extractability of manganese and iron oxides in typical Japanese soils by 0.5 mol L−1 hydroxylamine hydrochloride (pH 1.5)

We investigated the extractability of manganese (Mn) and iron (Fe) oxides from typical Japanese soils (Entisols, Inceptisols, and Andisols) by 0.5?mol?L^?1 hydroxylamine hydrochloride (NH₂OH-HCl) extraction (pH 1.5; 16?h shaking at 25°C; soil:solution ratio 1:40), referred as to HH_mBCR, which is Step 2 (used for the reducible fraction) of the modified BCR (Community Bureau of Reference) sequential extraction procedure. The HH_mBCR procedure extracted almost all Mn oxides from the non-Andisol samples, but failed to extract a part of the Mn oxides from some Andisol samples. The procedure extracted most short-range ordered Fe oxides from non-Andisol samples, but it extracted only 7.5% and 13% of the short-range ordered Fe oxides from allophanic and non-allophanic Andisol samples, respectively. This remarkably low extractability of Fe oxides suggests that the HH_mBCR method is not suitable for extracting oxide-occluded heavy metals from Andisols. Since the extraction rate of short-range ordered Fe oxides from various soils with the extractant was negatively correlated with the amounts of oxalate- and pyrophosphate-extractable Al even when the variability of the extraction pH was reduced by increasing the soil:solution ratio from 1:40 to 1:500, the extractability of Fe oxides would be negatively affected by the presence of active Al, including allophane/imogolite, amorphous Al, and Al-humus complexes. Because these Al constituents are abundant in Andisols, they would be at least partially responsible for the lower extractability of Fe oxides by HH_mBCR from Andisols.     

Soil podzolization induced by reforestation as shown by sequential and kinetic extractions of Fe and Al

The impact of 60‐year‐old reforestation on soil evolution was studied by following the evolution of Fe and Al distribution as an indicator of early podzolization. We determined the distribution of Al and Fe in soils by combining sequential and kinetic extractions. We extracted the soil sequentially with: 1 mol litre^?1 sodium acetate at pH 5.5 (stage 1); twice with 0.1 mol litre^?1 sodium pyrophosphate at pH 10 (stage 2 and 2b); and with 1 mol litre^?1 hydroxylamine in 4.3 mol litre^?1 acetic acid solution at 90°C (stage 3). For each, we drew a kinetic‐extraction curve. We show that no re‐adsorption, precipitation or complexation with dissolved organic matter occurred for the reaction times recommended in this procedure, that is 6 hours for stage 1, 1.5 hours for stage 2 and 2b and 3 hours for stage 3. For a given extraction, the kinetic curves have the same shape for all samples, that is their behaviour is similar for a given reagent. Sequential extraction can therefore be used to compare the speciation of metals in different samples taken from the same soil. In addition, 60 years after reforestation by beech, a decrease of 12 and 17% is noted in the total Fe and Al contents, respectively, in the 0–10 cm layer, accompanied by a re‐distribution of these elements within the different soil compartments: a decrease of the Fe and Al bound to oxy‐hydroxide in favour of organic complexes and more soluble forms. Sequential extraction is therefore a good indicator of the first pedogenetic modifications induced by human intervention through reforestation.     

Speciation and sorption structure of diphenylarsinic acid in soil clay mineral fractions using sequential extraction and EXAFS spectroscopy

Purpose

The mobility of arsenic (As) in soils is fundamentally affected by the clay mineral fraction and its composition. Diphenylarsinic acid (DPAA) is an organoarsenic contaminant derived from chemical warfare agents. Understanding how DPAA interacts with soil clay mineral fractions will enhance understanding of the mobility and transformation of DPAA in the soil-water environment. The objective of this study was to investigate the speciation and sorption structure of DPAA in the clay mineral fractions.

Materials and methods

Twelve soils were collected from nine Chinese cities which known as chemical weapons burial sites and artificially contaminated with DPAA. A sequential extraction procedure (SEP) was employed to elucidate the speciation of DPAA in the clay mineral fractions of soils. Pearson’s correlation analysis was used to derive the relationship between DPAA sorption and the selected physicochemical properties of the clay mineral fractions. Extended X-ray absorption fine structure (EXAFS) L_III-edge As was measured using the beamline BL14W1 at Shanghai Synchrotron Radiation Facility (SSRF) to identify the coordination environment of DPAA in clay mineral fractions.

Results and discussion

The SEP results showed that DPAA predominantly existed as specifically fraction (18.3–52.8%). A considerable amount of DPAA was also released from non-specifically fraction (8.2–46.7%) and the dissolution of amorphous, poorly crystalline, and well-crystallized Fe/Al (hydr)oxides (20.1–46.2%). A combination of Pearson’s correlation analysis and SEP study demonstrated that amorphous and poorly crystalline Fe (hydr)oxides contributed most to DPAA sorption in the clay mineral fractions of soils. The EXAFS results further demonstrated that DPAA formed inner-sphere complexes on Fe (hydr)oxides, with As-Fe distances of 3.18–3.25 Å. It is likely that the steric hindrance caused by phenyl substitution and hence the instability of DPAA/Fe complexes explain why a substantial amount of DPAA presented as weakly bound forms.

Conclusions

DPAA in clay mineral fractions predominantly existed as specifically, amorphous, poorly crystalline, and crystallized Fe/Al (hydr)oxides associated fractions. Amorphous/poorly crystalline Fe rather than total Fe contributed more to DPAA sorption and DPAA formed inner-sphere complexes on Fe (hydr)oxides.