The fate of freshly added phosphorus in representative agricultural soils

Surface and subsurface samples from 26 representative agricultural soils (13 Entisols, 9 Alfisols and 4 Vertisols) from Central and South Western Greece were equilibrated for a week with P solutions ranging from zero to 800 mg P kg^?1 soil. The Freundlich and in the cases of high fine carbonate content (> 6%) the linear equations described the sorption isotherms in a satisfactory way. Sequential fractionation indicated that a 0.1 M NaOH plus 1 M NaCl + 0.3 M Na-citrate + 1 M NaHCO₃ (buffer) solution extracted more than 60% of the P retained by Entisols containing low to medium fine carbonates and by Vertisols, and less than 60% by Entisols with a high fine carbonate content. In all Entisols, this percentage decreased significantly at P additions higher than 150 mg kg^?1. The opposite was observed in Vertisols, in which this fraction was the most important part of the retained P up to the maximum P addition. In contrast, in Alfisols this fraction reached 100%, but in the case of high Bray-P (> 50 ppm) it was more than 100% of the retained P. The second fraction extracted with the 0.3 M Na-citrate + 1 M NaHCO₃ buffer plus Na-dithionite was found to be much smaller than the first fraction, increasing with P additions in absolute amounts but remaining constant as a percentage of the retained P, ranging from 15–35% among the studied samples. The third fraction obtained with 1 M HCl solution showed a peculiar behaviour. It was close to zero of the retained P in samples containing carbonates (Entisols and Vertisols) at P additions up to 300 mg kg^?1 soil, but increased significantly at higher P additions and almost doubled in Entisols. Finally, the P fraction obtained after seven successive extractions with 0.01 M CaCl₂, correlated well by a polynomial of 2nd degree equation with NaOH+CB-P and linearly with Olsen-P and Bray-P.     

Verhalten von Schwermetallen in Böden 1. Untersuchungen zur Schwermetallmobilität

Behaviour of heavy metals in soils. 1. Heavy metal mobility 158 soil samples with widely varying composition were analysed for their total, EDTA, DTPA and CaCl₂ extractable contents of Cd, Zn, Mn, Cu and Pb. By means of single and multiple regressions the relations between the different heavy metal fractions and the pH, organic carbon and clay content were considered. The correlations between the total, EDTA and DTPA extractable contents are very close, whereas the CaCl₂ extractable contents are not or only weakly correlated with these fractions. According to these statistical results the former fractions are considered to be the total quantity (total content) and the reactive quantity (EDTA and DTPA extractable contents) of the heavy metals, whereas the CaCl₂ extractable fraction represents the mobile fraction of the heavy metals in soils. The multiple regressions show that the mobile content of heavy metals is closely correlated with each of the quantity fractions and with soil pH. In the same way the proportion of the mobile fraction (in %) of the total, EDTA and DTPA extractable heavy metal content of the soil samples is closely related to the soil pH. Hereby the proportion of the mobile content of the various elements increases in the pH range 6,5 - 3 below element-specific threshold pH values (in brackets) in the order Cd (6,5) > Mn (5,7) > Zn (5,3) > Cu (4,5) > Pb (3,5). In the pH range 6,5 - 7,5 mainly Cu and to a lesser degree also Pb show an increasing mobility due to the influence of soluble organic substances.     

Extractable Silicon in Soils of the South African Sugar Industry and Relationships with Crop Uptake

Reports of sugarcane yield responses to silicon (Si), coupled with mounting evidence that elevated crop Si levels reduce both biotic and abiotic stresses, account for the interest in the Si nutrition of this crop. In terms of managing Si supplies to sugarcane in South Africa, uncertainties exist regarding, first, the reserves of plant-available Si in soils, and second, the reliability of soil-test methods for predicting Si availability. In this study, extractable Si was measured in 112 soils collected from sugarcane-producing fields in South Africa. Soils were selected on the basis of dominant soil types and included Inceptisols, Alfisols, Mollisols, Vertisols, Oxisols, Entisols, and Ultisols, varying widely in chemical properties, texture, and extent of weathering. Extractants employed were 0.01 M calcium chloride (CaCl₂) and 0.02 N sulfuric acid (H₂SO₄). Silicon extracted with 0.02 N H₂SO₄ ranged from 2 to 293 mg kg^?1, whereas with 0.01 M CaCl₂ the range was 5 to 123 mg kg^?1. With both extractants, extractable Si decreased significantly with decreasing pH, exchangeable calcium (Ca), and total cations. In soils with potassium chloride (KCl)–extractable Al+H levels of greater than 0.5 cmol_cL^?1, extractable Si levels were consistently low, suggesting that soluble Al is implicated in reducing plant-available Si levels. Extractable Si levels were not related to the Bache and Williams P-sorption indices of soils. In the second part of the investigation, sugarcane leaf Si concentrations from 28 sites were related to soil extractable Si levels. The CaCl₂ soil test proved markedly superior to H₂SO₄ as a predictive test for leaf Si levels.     

Nutrients,Trace Elements and Net N Mineralization in Acidic Kenyan Soils

The nutrients status and properties in Kenyan soils (Kiambu, Mbeere Districts) are reported with the aim to elucidate the factors of productivity decline. According to the FAO (1988) system the studied soils were classified as humic Nitisols, haplic Acrisols or luvic Arenosols. The soils were found acidic, as a result of leaching of exchangeable cations and they are poor in organic carbon. Cation exchange capacity was extremely low in the sandy soils of Mbeere. Available phosphorus and exchangeable K⁺ were low inducing a crucial problem of soil fertility. Among the micronutrients, manganese extracted by DTPA was most abundant element, while micronutrients extracted by 4 M HNO₃ ranked as follows: Fe>Mn>Zn>Cu. Copper (DTPA) was low and manganese was extremely high in Kiambu. Iron content varied greatly, while decreased zinc was observed in Mbeere. Nitrogen mineralization over an incubation period of 30 weeks ranged from 54.64 to 145.50 mg kg^?1 and represents 4.53–21.09% of the total soil nitrogen. Soil nitrogen was associated to soil organic carbon and was strongly correlated to total soil N. Water harvesting, liming, and improved management of composting and manure are amongst the measures to restore soil fertility.     

Soil Properties Influence Distribution of Extractable Boron in Soil Profile

Depth distribution of boron (B) extractable by hot calcium chloride (HCC), potassium dihydrogen phosphate (PDP), and tartaric acid (TA) in some typical B‐deficient Inceptisols, Entisols, and Alfisols in relation to soil properties was studied. The magnitude of B extraction followed the order HCC > PDP > TA for Inceptisols, TA > HCC > PDP for Entisols, and PDP > HCC > TA for Alfisols and showed a decrease along soil depth. The low pH of TA and effective desorption of B by phosphate of PDP are attributed to their higher efficiency in extracting B in Entisols and Alfisols, respectively. A decrease in organic carbon (C), clay, and amorphous iron oxide content was responsible for the observed decrease in extractable B along depth of soil profile. The HCC showed more efficiency than PDP and TA for extracting B in soils high in organic C. Multiple regression equations explained only 21, 57, and 59% of the variability in PDP‐, HCC‐, and TA‐extractable B content in soils by the soil properties analyzed, of which organic C and clay were the most important. There were dynamic equilibria among the amount of B extracted by the extractants, indicating B extraction by them from more or less similar pools in the soils.     

Bestimmung von Mikronährstoffen und Schwermetallen in Böden mit dem Verfahren der Elektro‐Ultrafiltration (EUF) durch Zugabe von DTPA

With the electro–ultrafiltration (EUF) technique, the plant availability of several plant nutrients in soils can be characterized. The basic principle of EUF is that an electric field is induced using platinum electrodes. Ions in the soil suspension move either to the cathode or to the anode and are filtrated through ultra‐membrane filters. In the standard EUF procedure, two extractions steps are used: 30 min at 20°C and 5 min at 80°C. However, the determination of micronutrients and heavy metals with the standard EUF procedure is not possible, because the solubility of these elements in water is low and most of the watersoluble elements are precipitated when passing the platinum electrodes. The addition of DTPA, a well known complexing agent, during a third EUF fraction (5 min at 80°C) enables extraction of micronutrients and heavy metals. Highest concentrations in the 33 soils of the study were found for iron, followed by zinc, manganese, lead, copper, and nickel. Lower concentrations were obtained for cobalt, chromium, cadmium, and molybdenum. For two soils, the EUF/DTPA procedure was compared to CaCl₂/DTPA and EDTA soil extraction methods, showing that higher or comparable amounts were found with CaCl₂/DTPA and much higher amounts with the EDTA method. These results reveal that the EUF/DTPA technique in principle can be used for the determination of plant‐available micronutrients and heavy metals. However, in a next step the relationship between EUF/DTPA‐extractable elements and their availability for plants needs to be quantified.     

An evaluation of chemical methods for extracting copper from rice soils

Abstract

Rice (Oryza sativaL. CV. Lemont) was grown on 19 soils, and eight extractants were evaluated for determining the availability of Cu to rice plants. Correlation analyses were employed as criteria for evaluating methods that would provide the best index of Cu availability. The order of removal of Cu from soils was: 0.5NHC1 + 0.05NA1C1₃> 0.5NHNO₃> 0.5 N HC1 > EDTA + NH₄OAc > 0.1NHC1 > EDTA + (NH₄)₂CO₃? DTPA‐TEA, pH 7.3 >>> 1 N NH₄0Ac, pH 4.8.

Uptake of Cu by rice plants was significantly correlated with soil Cu. Among the eight extractants evaluated, Cu extracted with DTPA‐TEA, pH 7.3 was better related to the concentration (r = 0.563 ) and uptake (r = 0.673 ) of Cu by rice plants grown on the soils with different chemical and physical properties.

A significant negative correlation was found between the concentration of Cu in rice plants and the organic matter content of the soils. Each one percent increase in the organic matter of the soils resulted in a corresponding decrease of approximately one mg/kg in the concentration of Cu in the rice‐plant tissue. Multiple regressions of extractable Cu by eight methods with soil organic matter content accounted for from 53.4 to 70.0% of the variations in the prediction of the concentration of Cu in the rice plants. Combinations of other soil chemical properties measured with extractable Cu did not significantly improve the predictability     

Micronutrients distribution in salt-affected soils of the Punjab in relation to soil properties

Salt-affected soils in arid and semi-arid tracts of the Indian Punjab are prone to deficiency of micronutrients. Nine profiles from alluvial terraces, sand dunes and palaeochannels in the southwestern Punjab were investigated for total and diethylenetriamine-penta-acetic acid (DTPA) extractable Zn, Cu, Mn and Fe. Soil physiography exerted significant influence on the spatial distribution of micronutrients. Total contents varied from 20–78 for Zn, 8–32 for Cu, and 88–466 mg kg^?1 for Mn and 0.82–2.53% for Fe. DTPA-extractable contents varied from 0.10–0.98 for Zn, 0.14–1.02 for Cu, 0.54–13.02 for Fe and 0.82–9.4 mg kg^?1 for Mn. Total contents were higher in fine-textured soil than in coarse-textured soils. Concentration of micronutrients in the surface layer was low and there occurred more accumulation in the Cambic horizon. Organic carbon, pH, clay, silt and calcium carbonate exerted strong influence on the distribution of micronutrients. DTPA extractable Zn, Cu, Mn and Fe increased with increasing organic carbon but decreased with increase in pH and calcium carbonate content. Total micronutrient contents increased with increase in clay, silt and calcium carbonate contents and decreased with increase in sand content.     

Trace elements in Bangladesh paddy soils

Abstract

A study was carried out to investigate the status of four micronutrients, iron (Fe), copper (Cu), manganese (Mn), and zinc (Zn), and five other trace elements, cobalt (Co), chromium (Cr), nickel (Ni), lead (Pb), and strontium (Sr), in paddy soils of Bangladesh. Soil samples were digested by hydrofluoric acid (HF)‐nitric acid (HNO₃)‐perchloric acid (HClO₄) for determination of total contents of the nine elements, while DTPA, ASI and 0.1 Mhydrochloric acid (HC1) methods were used for determination of available Fe, Cu, Mn, and Zn. Total trace element contents were found to vary with physiography on which soils are distributed. In general, Ganges Tidal Floodplain soils had the highest content, whereas terrace soils had the lower content. Among the soil properties examined, clay content had a good relation with total trace element contents in the topsoil, except for Sr. Based on the variation with physiography or clay content, the nine trace elements could be grouped into six groups: Cu, Fe and Zn, Pb, Co and Cr and Ni, Mn, Sr. According to the extractable levels of four micronutrients, Bangladesh paddy soils had the medium to optimum amounts of Fe and Cu, but were deficient sporadically in Mn and extensively in Zn. It was indicated that paddy soils of Bangladesh are yet to be polluted with heavy metals.     

Distribution of Forms of Zinc and Their Association with Soil Properties and Uptake in Different Soil Orders in Semi‐arid Soils of Punjab,India

Abstract

Profiles of semi‐arid–zone soils in Punjab, northwest India, were investigated for different forms of zinc (Zn), including total, diethylenetriamine penta‐acetic acid (DTPA)-extractable, soil solution plus exchangeable (Zn), Zn adsorbed onto inorganic sites, Zn bound by organic sites, and Zn adsorbed onto oxide surfaces. Irrespective of the different fractions of Zn present, its content was higher in fine‐textured Alfisols and Inceptisols than in coarse‐textured Entisols. In general, the higher content of Zn was observed in the surface horizon and then decreased in the subsurface horizons. However, none of the forms of Zn exhibited any consistent pattern of distribution. Organic matter and size fractions (clay and silt) had a strong influence on the distribution of different forms of Zn. Based upon the linear coefficient of correlation, the soil solution plus exchangeable Zn, adsorbed onto inorganic sites, and DTPA‐Zn increased with increase in organic carbon but decreased with increase in pH and calcium carbonate content. Total Zn increased with increase in clay and silt content. Among the different forms, Zn bound by organic sites, water soluble plus exchangeable Zn and Zn adsorb onto oxide (amorphous surfaces) were all correlated with DTPA extractable Zn. The uptake of Zn was more in recent floodplain Entisols than very fine textured Alfisols and Inceptisols. Among the different forms soil solution +exchangeable and DTPA‐extractable Zn was positively correlated with total uptake of Zn.     

Distribution of Forms of Copper and their Association with Soil Properties and Uptake in Major Soil Orders in Semi-arid Soils of Punjab,India

Profiles of semi-arid-zone soils in Punjab, northwestern India, were investigated for different forms of copper (Cu), including total Cu, diethylenetriaminepentaacetic acid (DTPA)–extractable Cu, soil solution plus exchangeable Cu, Cu adsorbed onto inorganic sites, Cu bound by organic sites, and Cu adsorbed onto oxide surfaces. When all soils were considered, total Cu content ranged from 7 to 37 mg kg^?1, while DTPA-extractable and soil solution plus exchangeable Cu contents ranged from 0.30 to 3.26 mg kg^?1 and from 0.02 to 0.43 mg kg^?1, respectively. Copper adsorbed onto inorganic sites ranged from 0.62 to 2.6 mg kg^?1 and that onto oxide surfaces ranged from 2.0 to 13.2 mg kg^?1. The Cu bound by organic sites ranged from 1.2 to 12.2 mg kg^?1. The magnitudes of different forms of Cu in soils did not exhibit any consistent pattern of distribution. Organic matter and size fractions (clay and silt) had a strong influence on the distribution of different forms of Cu. The content of all forms of Cu was generally greater in the fine-textured Alfisols and Inceptisols than coarse-textured Entisols. Soil solution plus exchangeable Cu, Cu held onto organic sites, and and Cu adsorbed onto inorganic sites (crystalline) had significant positive correlations with organic carbon and silt contents.The DTPA Cu was positively correlated with organic carbon, silt, and clay contents. Total Cu content strongly correlated with silt and clay contents of soils. Among the forms, Cu held on the organic site, water soluble + exchangeable Cu, and Cu adsorbed onto oxide surface were positively correlated with DTPA-extractable Cu. The DTPA-extractable Cu and soil solution plus exchangeable Cu seems to be good indices of Cu availability in soils and can be used for correction of Cu deficiency in the soils of the region. The uptake of Cu was greater in fine-textured Inceptisols and Alfisols than coarse-textured Entisols. Among the different forms only DTPA-extractable Cu was positively correlated with total uptake of Cu.     

Prediction of Soil Cadmium Bioavailability to Cacao (Theobroma cacao L.) using Single-Step Extraction Procedures

In this study, complexation extractants ammonium bicarbonate diethylene triamine pentaacetic acid (AB-DTPA), diethylene triamine pentaacetic acid (DTPA), and ethylene diamine tetraacetic acid (EDTA) and mild cation-exchange extractants calcium chloride (CaCl₂) and ammonium nitrate (NH₄NO₃) were used to evaluate the bioavailability of soil cadmium (Cd) to cacao in the field. Among the five extractants, the extractable Cd generally followed the order EDTA > DTPA > AB-DTPA > CaCl₂ > NH₄NO₃. Correlation analysis was done between the extractable Cd in soil and total Cd content of cacao tissues (nibs, shells, leaves, and pods). The Cd extracted by CaCl₂ and NH₄NO₃ was significantly (P < 0.05) correlated with some of the tissues but their Pearson correlation coefficients were weak. In contrast, extractants AB-DTPA, DTPA, and EDTA showed stronger, significant correlations to the Cd concentration in all four tissues. Overall, regression analysis demonstrated that AB-DTPA, DTPA, or EDTA can be used to predict bioavailable Cd in soils for cacao. Of these, AB-DTPA and DTPA both showed the strongest correlations compared to EDTA. However, the ease of preparation and the superior shelf-life of DTPA over AB-DPTA make it the preferred reagent for Cd bioavailability extractions from cacao soils and is currently being used to develop cost-effective soil treatments to reduce bioavailable Cd to cacao plants.     

The classification, distribution, and extent of soils with a xeric moisture regime in the United States

Soils with cool, moist winters and relatively warm, dry summers, a Mediterranean climate, are recognized as having a xeric moisture regime in Soil Taxonomy. These soils are classified mostly in taxa that use the formative element “xer” in the name. Soil series with either a xeric moisture regime or an aridic regime bordering on a xeric moisture regime make up more than 48,640,000 hectares in the western part of the United States. They are classified in the orders of Mollisols (20,080,000 ha), Aridisols (11,200,000 ha), Alfisols (5,320,000 ha), Inceptisols (4,800,000 ha), Entisols (4,400,000 ha), Vertisols (1,520,000 ha), Andisols (960,000 ha), and Ultisols (960,000 ha).     

Appraisal of Some Soil Tests for Zinc Availability to Late‐Sown Wheat Grown in Mollisols

Abstract

Five soil extractants, namely, 0.005 M diethylene triamine pentaacetic acid (DTPA) (pH 7.3), 0.005 M DTPA+1 M ammonium bicarbonate (pH 7.6), Mehlich 3, 0.01 M ethylene diamine tetraacetic acid (EDTA)+0.05 M ammonium carbonate (pH 8.6), and 1 M magnesium chloride (MgCl₂) (pH 6.0), were evaluated to predict the response of wheat to zinc (Zn) application in Mollisols. These extractants could be arranged in the following decreasing order of their Zn extracting power: Mehlich 3>0.005 M DTPA+1 M ammonium bicarbonate>0.01 M EDTA+0.05 M ammonium carbonate>0.005 M DTPA>1 M MgCl₂. The critical limits of Zn in soil, below which the yield response to late sown wheat (var. UP‐2338) to Zn application could be expected, were 0.57 mg 0.005 M DTPA (pH 7.3) extractable and 1.72 mg Mehlich 3–extractable Zn kg^?1 soil. The critical limit of Zn in whole shoot at 60 days after emergence was found to be 26.1 mg Zn kg^?1 plant tissue. The DTPA and Mehlich 3–extractable soil Zn also correlated significantly and positively with Zn concentration in whole shoot at 60 days after emergence and total Zn uptake by wheat at harvest.     

Soil‐plant relationships,micronutrient contents,and cardenolide production in natural populations of Digitalis obscura

The production of secondary metabolites by plants growing in natural populations is conditioned by environmental factors. In the present study, we have investigated the relationships among soil properties, micronutrients in soils and plants, and cardenolide production from wild Digitalis obscura (Scrophulariaceae) populations. Young and mature leaves and soil samples were collected in ten different populations, corresponding to three Mediterranean bioclimatic belts (Thermo‐, Meso‐, and Supramediterranean belts). Soil (total and EDTA‐extractable) and leaf micronutrients (Fe, Mn, Zn, and Cu), and leaf cardenolide accumulation have been determined. Significant negative correlations were observed between Fe, Mn or Zn concentration in leaves and soil pH, as well as between Fe or Mn in leaves and carbonate content of soils. Only EDTA‐extractable Mn was significantly correlated with Mn content in the plants. With regard to cardenolide content in leaves, this parameter was negatively correlated with Zn_leaf in young leaves and with Mn_leaf in old leaves. Positively correlated, however, were Fe and cardenolide content in young leaves. The influence of environmental conditions and leaf micronutrient contents on cardenolide accumulation is discussed.     

Patterns and classification by soil taxonomy of the soils of the southern cook islands

The soil patterns of the six larger islands of the Southern Cook Group in the South Pacific are described. Classification is according to Soil Taxonomy, and six soil orders are recognised: Oxisols, Ultisols, Mollisols, Alfisols, Inceptisols and Entisols, which are further subdivided into 12 suborders, 15 great groups, and 25 subgroups. Classification to series level is outlined in tabular form. The soil pattern on individual islands is basically one of concentricity. The older, more weathered soils (Oxisols and Ultisols) occur on remnant surfaces and grade with either decreasing altitude or age of land surface to Alfisols, Mollisols, Inceptisols, and Entisols, respectively. Many of the soils associated with the coralline makateas have shallow contacts to the underlying limestone and have been separated in lithic subgroups.     

Verhalten von Schwermetallen in Böden. 2. Extraktion mobiler Schwermetalle mittels CaCl2 und NH4NO3

Behaviour of heavy metals in soils. 2. Extraction of mobile heavy metals with CaCl₂ and NH₄NO₃ 156 soil samples from arable fields, grassland and forest stands were analysed for the CaCl₂^? and NH₄NO₃^? extractable contents of Cd, Zn, Mn, Cu and Pb. The average amounts of Cd, Zn, Cu and Pb extracted with CaCl₂ are higher compared with NH₄NO₃ whereas the relation for Mn is vice versa. The proportion of the NH₄NO₃^? extractable contents in percent of the CaCl₂^? extractable contents of Cd, Zn and Pb decrease with increasing pH, whereas the contents of Mn and Cu increase. Inspite of a differing extraction behaviour of the two salt solutions the CaCl₂^? and NH₄NO₃^? extractable amounts of Cd, Mn, Zn und Pb are highly correlated and can be converted one into another. The mobile (CaCl₂, NH₄NO₃) proportion of the corresponding total, EDTA and DTPA heavy metal contents is in close relation to the pH of the soils. Using CaCl₂ solution the threshold pH values for an increasing mobility decrease in the order Cd > Mn > Zn > Cu > Pb, using NH₄NO₃ as extractant the order is Mn > Cd > Zn > Cu > Pb. In the case of CaCl₂ as extractant soluble chloro-Cd-complexes will be formed so that the Cd mobility in soils will be overestimated in most cases.     

Use of NH4 HCO3‐DTPA soil test to assess availability and toxicity of selenium to alfalfa plants

Abstract

This study was carried out to determine if ammonium bicarbonate‐DTPA soil test (AB‐DTPA) of Soltanpour and Schwab for simultaneous extraction of P, K, Zn, Fe, Cu and Mn can be used to determine the availability index for Se. Five Mollisols from North Dakota were treated with sodium selenate and were subjected to several wetting and drying cycles. These soils were extracted with hot water and with ammonium bicarbonate‐DTPA (AB‐DTPA) solution for Se analysis. Alfalfa plants were grown in these soils in a growth chamber to determine plant uptake of Se. In addition to the above experiment, coal mine soil and overburden materials from Western Colorado were extracted and analyzed as mentioned above.

It was found that hot water and AB‐DTPA extracted approximately equal amounts of Se from Mollisols. A high degree of correlation (r =0.96) was found between Se uptake by plants and AB‐DTPA extractable Se. Extractable level of Se in treated soils was decreased with time due to change of selenate to less soluble Se forms and plant uptake of Se. An AB‐DTPA extractable Se level of over 100 ppb produced alfalfa plants containing 5 ppm or higher levels of Se that can be considered toxic to animals. Soils with about 2000 ppb of extractable Se were highly toxic to alfalfa plants and resulted in plant concentrations of over 1000 ppm of Se. The high rate of selenate (4ppm Se) was less toxic to alfalfa plants in soils of high organic matter content. This lower toxicity was accompanied with lower extractable levels of Se.

The AB‐DTPA solution extracted on the average about 31% more Se than hot water from the mine and overburden samples and was highly correlated with the latter (r =0.92). The results indicated the presence of bicarbonate‐exchangeable Se in these materials.     

Effects of soil flooding on P transformations in soils of the Mesopotamia region,Argentina

In the Mesopotamia region (Argentina), rice is cropped on a wide range of soil types, and the response of rice to fertilizer application has been inconsistent even in soils with very low levels of available phosphorus. Phosphorus transformations in flooded soils depend on soil characteristics that may affect phosphorus availability. This study was conducted to determine which soil characteristics were related to the changes in P fractions during soil flooding. Soils were chosen from ten sites within the Mesopotamia region that are included in five different soil orders: Oxisols, Ultisols, Alfisols, Mollisols, and Vertisols. Soil phosphorus (P) was fractionated by a modified Hedley method before and after a 45 d anaerobic‐incubation period. Changes in the inorganic P extracted with resin depended on soil pH and were related to the exchangeable‐Fe concentration of soils (extracted with EDTA). Inorganic P extracted with alkaline extractants (NaHCO₃ and NaOH) increased due to soil flooding. This increase was related to the organic‐C (OC) percentage of soils (r² = 0.62, p < 0.01), and ranged from 13 to 55 mg kg^–1. Even though previous studies showed that P associated with poorly crystalline Fe played an important role in the P nutrition of flooded rice, in this study, there was no relationship between ammonium oxalate–extractable Fe and P changes in soils due to flooding. Our results suggest that in the Mesopotamia region, changes in P fractions due to soil flooding are related to soil OC, soil pH, and soluble and weakly adsorbed Fe.     

Extractable Micronutrients Status of Soils in a Plinthitic Landscape at Zaria,Nigeria

Desilication and leaching are processes that accompany plinthilization, leading to nutrient depletion. Soils from 12 profiles in a plinthitic landscape were analyzed for extractable micronutrients [iron (Fe), zinc (Zn), manganese (Mn), and copper (Cu)]. Soils of the landscape from crestal to lower‐slope position contain plinthite in the profile, whereas those of the valley floor are devoid of plinthite. The micronutrients were extracted using diethylenetriaminepentaacetic acid (DTPA) and 0.1 M hydrochloric acid (HCl). The results showed that 0.1 M HCl extracted more of the micronutrients than DTPA. The DTPA‐extractable Fe, Zn, Mn, and Cu in all the soils ranged from 1.15 to 12.44 (mean, 3.69); 0.71 to 2.75 (mean, 1.86); trace 12.44 (mean, 3.35), and trace 3.76 (mean, 0.63) mg kg^?1, respectively. The DTPA‐extractable micronutrient contents were generally greater than the critical available level (4.5 mg kg^?1 for Fe, 0.8 mg kg^?1 for Zn, 1.0 mg kg^?1 for Mn, and 0.2 mg kg^?1 for Cu). The 0.1 M HCl‐extractable micronutrients in the landscape ranged from 8.00 to 30.40 (mean, 15.19); 0.30 to 6.49 (mean, 1.35); 1.00 to 27.20 (mean, 7.74); and 0.26 to 15.0 (mean, 2.77) mg kg^?1 for Fe, Zn, Mn, and Cu, respectively. Both DTPA‐ and 0.1 M HCl‐extractable micronutrients were generally lower in the plinthitic horizons than in the nonplinthitic horizons and higher in the Ap than the subsoil horizons. Correlation analysis showed a significant relationship between DTPA‐Fe and DTPA‐Mn, Cu, and organic carbon (r = 0.913**, 0.411**, and 0.385**). There was a significant and positive relationship between 0.1 M HCl‐extractable Mn and organic carbon (C), total nitrogen (N), and available phosphorus (P) (r = 0.413**, 0.337**, and 0.350**, respectively).