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1.
Abstract

Surface horizons from Podzolic and Gleysolic soils were collected in various parts of the province of Quebec, Canada, and equilibrated with various amounts of KH2PO4 in 0.01 M CaCl2 for 48 hours. P sorption data conformed to the linear form of the Langmuir and Freundlich equations. P solubility isotherms showed evidence of hydroxyapatite formation in most samples studied, whereas equilibration solutions of only few samples were saturated with respect to either dicalcium phoshate dihydrate or octocalcium phosphate. These reaction products were associated to soil pH and levels of added phosphate. The average values of the Langmuir sorption maximum for these studied Gleysolic and Podzolic samples were 763 and 1096 μg/g respectively. These values were higher than those obtained by the segmented and modified Freundlich models.

Relationships between the soil characteristics and P sorption parameters were evaluated by regression analysis. Among all variables, oxalate‐extractable Fe plus Al content of the Podzolic samples and the ratio of oxalate—extractable Al to clay of the Gleysolic samples gave the best significant correlation coefficients. Furthermore, soil pH and various ratios such as pyrophosphate‐extractable Fe and Al, oxalate‐extractable Fe and organic matter to clay were found to be significantly correlated only with the P sorption parameters of the Gleysolic samples.  相似文献   

2.
Abstract

Different forms of soil aluminum (Al) are involved in the retention of anions and cations, phytotoxicity of Al in acid soils, CEC reduction and soil physical properties such as aggregate stability and water infiltration. Therefore it is desirable to quantify the different forms of Al in soil especially acidic soils. A rationale was developed from a literature survey to identify the following fractions of Al: (a) exchangeable quantified by 1M KC1 extraction; (b) organic bound quantified by 0.1M CuCl2 + 0.5M KCl extraction; (c) sorhed Al extractable with 1M NE4OAc at pH 4.0; (d) amorphous Al oxide and hydroxide and amorphous aluminosilicates (if present) extractable with 0.2M ammonium oxalate at pH 3.0; and (e) interlayered Al extractable with 0. 33M sodium citrate at pH 7.3. Pools (a), (b), and (c) are extracted sequentially. Amorphous Al oxide and hydroxide (pool d) is calculated from ammonium oxalate extractable Al minus (a + b + c). Interlayered Al is calculated from sodium citrate extractable Al minus ammonium oxalate extractable Al. The latter two extractions are done on separate subsamples of soils. From preliminary studies and data for 13 soil samples it is suggested that this fractionation of soil Al is more meaningful than that obtained by the KCl ‐> K4P2O7 ‐> ammonium oxalate > citrate‐bicarbonate‐dithionite extraction sequence.  相似文献   

3.
Abstract

Phosphate (P) sorption characteristics of six natural Ghanaian Oxisols, selected because of their hydrological and topographical suitability for agriculture, were evaluated. Availability of P appears to be adequate for half of the soils as suggested by the Bray P1 test and determination of the standard P requirement (SPR), i.e., the amount of P sorbed at a concentration of 0.2 ppm P (6.46 μM). The SPR was found to be very closely related to Pmax (Langmuir P sorption capacity), which in turn, was significantly correlated with oxalate‐extractable aluminum (Al) (Alo) and iron (Fe) (Feo) and related (not significantly) to the difference between dithionite‐citrate‐bicarbonate‐extractable Fe (Fed) and oxalate‐extractable Fe. Accordingly, Pmax is fairly well predicted by the model of Borggaard: Pca]e=0.211#lbÀlo+0.115#lbFeo+ 0.05#lb(Fed‐Feo)+0.3, except for one soil strongly enriched in Fe oxides, mainly goethite. This goethite was found by X‐ray diffraction analysis to consist of crystals larger than normally found for pedogenic Fe oxides. The difference between Pmax and Pcalc for this soil could, therefore, be attributed to the occurrence of these large Fe oxide crystals, because P sorption will decrease with increasing crystal size (decreasing specific surface area).  相似文献   

4.
Abstract

Surface soils from ten soil series representing five great groups were collected from Alaska. These soils were selected from the important agricultural areas covering a wide geographic distribution. These soils can be divided into two distinct groups based on their parent material: loess and volcanic ash. Phosphorus sorption maxima were calculated based on the Langmuir isotherms. The volcanic ash soils (Cryandept and Cryorthods) showed an average P‐sorption maxima of 10,122 mg/kg and loess soils averaged 3,934 mg/kg. Both groups have similar portions of phosphorus in the organic form (19%) and occluded form (8 to 9%). The nonoccluded‐P in the volcanic ash soils and the loess soils was 68% and 43% respectively, and the Calcium‐P was 4% and 29% respectively.

Regression analysis indicated that aluminum and iron are primarily responsible for P‐sorption. The dithionite extractable Al is responsible for P‐sorption in volcanic ash soils, while oxalate extractable Al is responsible for P‐sorption in loess soils. Dithionite and oxalate extractable Fe probably play a secondary role in P‐sorption. The sorption isotherm, regression analysis and the P‐fractionation data provide the agronomist with useful information to estimate P requirement of newly cleared soils.  相似文献   

5.
Abstract

Few studies have utilized a statistical approach for the evaluation and comparison of breakthrough profiles obtained from soil column investigations. Our objective was to investigate the use of nonlinear estimation techniques to identify the phosphorus (P) breakthrough point and other parameters endemic to breakthrough data. Four soils exhibiting a range in physical and chemical properties were leached under saturated‐flow conditions with a 10 mg P/L solution for 34 d. Leachate P concentrations were analyzed by flow injection colorimetric analysis. A four‐parameter segmented exponential model provided a good fit for the breakthrough data in each soil tested. In addition to identifying the breakthrough point, the model parameters provided estimates of other identifiable aspects of a breakthrough profile including background P concentration, equilibrium P concentration, and the rate of concentration change once breakthrough is attained. Estimation of these parameters also facilitated statistical comparison of breakthrough profiles from different soils. Single and joint hypothesis tests showed that significant differences existed among the breakthrough profiles, the breakthrough points, and the rates of concentration change. Additionally, simulation was used to examine the correlation structure between the estimated breakthrough point and 17 soil properties. The simulation showed that 6 soil properties— ammonium oxalate extractable aluminum (Al) and iron (Fe), citrate dithionite extractable Al, CaCl2 and acetate extractable P, and P sorption capacity— were strongly correlated with P breakthrough.  相似文献   

6.
Abstract

Highly calcareous soils are abundant in Iran. The calcium carbonate equivalent (CCE) of these soils reach up to 650 g kg?1. Although phosphorus (P) fertilizer is being widely used in these soils, little information, if any, is available about P status in such soils. The objectives of this study were to 1) determine inorganic P forms in 18 surface soils of southern Iran, 2) study P readsorption during different stages of fractionation schemes, 3) assess the ability of NaOH to extract aluminum (Al)‐P, and 4) evaluate the relationships between P availability indices and inorganic P forms. Eighteen soil samples with a wide range of physicochemical properties were selected for this study. Inorganic P forms was determined by sequential extraction with NaHCO3, NH4OAc, NH4F, NaOH, citrate dithionite (CD), and H2SO4, which are referred to as Ca2‐P, Ca8‐P, Al‐P, Fe‐P, occluded P (O‐P), and Ca10‐P. Phosphorus readsorption in different stages was determined by 1 M MgCl2. Furthermore, a fractionation scheme without an NH4F step was used to evaluate the ability of NaOH to extract Al‐P. NaHCO3 (Olsen‐P) and MgCl2‐extractable P (Exch‐P) were regarded as P-availability indices. The abundance of different P forms was in the order Ca2‐P<Fe‐P<Al‐P<O‐P<Ca8‐P<Ca10‐P. Ca2‐P was highly correlated with Olsen‐P and Exch‐P. Ca2‐P, Olsen‐P, and Exch‐P showed a relationship with CCE, citrate–bicarbonate–dithionite extractable Fe (Fed), and Al (Ald). Phosphorus readsorption appeared to be important only in the Ca8‐P step, and the content of readsorbed P was related to Ca8‐P, CCE, and clay content of the soils. In the present study, Al‐P and Fe‐P accounted for 10 and 5% of the sum of the inorganic P fractions, respectively, and Fe‐P showed a strong relationship with Feo, whereas Al‐P showed a significant relationship with oxalate‐extractable Al (Alo) and Ald. It was found that one extraction with NaOH is not a good indicator for Fe‐ and Al‐P, and the ability of NaOH to extract Al‐P was reduced with increase in Al‐P content.  相似文献   

7.
The more labile forms of aluminium in a range of soils from areas of permanent grassland were determined with a number of selective extractants. The amounts of exchangeable A1 extracted with molar KCl were dependent upon pH, while the amounts exchangeable with 0.3 M LaCl3, although much greater, were not well correlated with pH. There were good correlations between soil organic C content and A1 extracted by (i) 0.5 M EDTA and (ii) 0.1 M potassium pyrophosphate. Pyrophosphate extracted greater amounts than any of the other extractants (sodium citrate/dithionite, ammonium oxalate (dark), acid oxalate (UV radiation), as well as those already mentioned). It was concluded that much of the extractable A1 in soils was associated with organic matter. Addition of lime to one of the soils reduced the amount of A1 extracted by all reagents except dithionite and acid oxalate solutions. There were considerable differences between soils in their release of A1 to continuous leaching with 0.01 M CaCl2. Despite these differences between the soils in organically bound extractable Al, the differences in the amounts and patterns of release of A1 with CaCl2 did not appear to be related to organic matter contents, nor to the other determined properties.  相似文献   

8.
Abstract

Acid oxalate reagent was used at various concentrations, pH values, shaking times, and soil to solution ratios to find the optimum conditions for the extraction of Al, Fe, and Si from short‐range‐order materials in soils and stream‐bed deposits. The optimum conditions vary with the nature of the soil sample and its components. For most soils maximum amounts of Al, Fe, and Si were extracted with 0.15M acid oxalate reagent at pH 3.0 with a soil to solution ratio of 1:100 and shaking for 4 h in the dark at 20°C. Soils with more than 5% oxalate‐extractable Al or Fe require a 0.20M oxalate solution at pH 3.0 with a soil to solution ratio of 1:200.

Allophane is extracted by acid oxalate reagent after shaking for 2 h and it may be estimated from the 4 h oxalate‐extractable Si values. Ferrihydrite is extracted after shaking for 4 h, and it may be estimated from the oxalate‐extractable Fe values. Either sodium oxalate or ammonium oxalate may be used  相似文献   

9.
Abstract

Phosphorus sorption studies were conducted on volcanic ash influenced surface horizons of 29 northern Idaho soils. Results show that the amount of P sorbed was significantly correlated with citrate‐dithionite extractable aluminum (r = .64**), but not with Fe. Other significantly correlated soil properties were: percent base saturation (r = ‐.73**), percent clay (r = .42**), and exchangeable acidity (r = .39*).  相似文献   

10.
Abstract

We compared sequential and separate extraction procedures for estimating non‐crystalline and crystalline aluminum (Al) and iron (Fe) in a floodplain forest soil. We used 0.2M acid ammonium oxalate (pH 3.0) to estimate non‐crystalline Al and Fe, dithionite‐citrate‐bicarbonate to estimate crystalline Fe, and 0.1M sodium hydroxide (NaOH) to estimate crystalline Al. Both separate and various combinations of sequential extractions were compared, as well as variations in soil:solution ratio, extraction time, extraction temperature, and the use of field‐moist versus dried soils. A sequential oxalate/NaOH extraction, using 0.4 g dry weight equivalent of field‐moist soil and a soil:solution ratio of 1:100, gave the best estimate of non‐crystalline Al and Fe and crystalline Al, while a separate 16 hour DCB extraction at room temperature, using 0.8 g dry weight equivalent of field‐moist soil and a soil:solution ratio of 1:50, gave the best estimate for non‐crystalline plus crystalline Fe. A sequential oxalate/NaOH extraction followed by a separate DCB extraction is a relatively simple procedure for estimating amounts of non‐crystalline and crystalline Al and Fe in large numbers of soil samples.  相似文献   

11.
Abstract

Phosphate sorption isotherms were determined for 16 representative major soils developed from different parent materials on Okinawa. Phosphate sorption characteristics were satisfactorily described by the Langmuir equation, which was used to determine phosphorus (P) sorption maxima of the soils. Phosphate sorption maxima ranged from 630 to 2208 mg P kg‐1 soil (mean 1,362 mg P kg‐1). The standard P requirement (i.e., the amount of P required to attain 0.2 mg P L‐1 equilibrium solution) followed the same trend as sorption maximum (r =0.94***), with values ranging from 132 to 1,020 mg P kg‐1 soil (mean 615 mg P kg‐1). This mean value corresponds to fertilizer addition of 923 kg P ha‐1 indicating that the soils have high P fertilizer requirements. Results of simple linear regression analysis indicated that sorption maximum was significantly correlated with clay content, organic matter, oxalate iron (Fe), pyrophosphate Fe, DCB aluminum (Al), oxalate Al, and pyrophosphate Al, but not with DCB Fe, pH, or available P content. The best regression model for predicting sorption maximum was the combination of clay, organic matter, pyrophosphate Fe, and DCB Al which altogether explained 79% of the variance in sorption maximum. The equation obtained could offer a rapid estimation of P sorption in Okinawan soils.  相似文献   

12.
Abstract

The importance of various soil components on copper (Cu) retention by Spodosois was investigated. Copper sorption and extraction were conducted on samples from the B horizon from six Danish Spodosois. The investigation was conducted on untreated samples, on hydrogen peroxide‐treated samples (to remove organic matter), on oxalate‐treated samples [to remove amorphous to poorly crystalline aluminum (Al) and iron (Fe) oxides], on hydroxylamine‐treated samples [to remove manganese (Mn) oxides]. Subfractions treated with hydrogen peroxide (H2O2) were further treated with oxalate and citrate‐bicarbonate‐dithionite (CBD). Sorption of Cu from an initial 10‐6 M solution after 48 hours was determined in the pH range 3 to 7 using 0.1M sodium nitrate (NaNO3) as the background electrolyte. The pH‐dependent sorption curve (sorption edge) was shifted to a higher pH with decreasing Al oxide content in the soils, and for the treated sample after removal of organic matter and Al and Fe oxides. A negligible effect was seen after removal of the Mn oxides because of their low abundance. Extraction of sorbed Cu at pH 4 to 6 with 0.1M nitric acid (HNO3) for 24 hours confirmed the sorption results, in inasmuch as removal of the Al (and Fe) oxides increased Cu extractability. Therefore, it was concluded that in the soils investigated, Cu retention is mainly determined by the oxalate‐extractable Al fraction with a minor contribution due to crystalline Fe oxides.  相似文献   

13.
Abstract

The efficiency of Mehlich‐3 reagent as an extractant for aluminum (Al) and iron (Fe) was studied in Galician coal mine soils, in the process of reclamation. Mehlich‐3 Al and Fe values were compared to those from other Al and Fe tests and with phosphorus (P) sorption. The soils are very heterogeneous, consisting mainly of carbonaceous and non‐carbonaceous clays and shales, which are often rich in pyrite. Some of them have been amended with topsoil or fly ash. One hundred forty samples, from 0 to 15 or 15 to 30 cm, were analyzed. The pH values ranged from 2.7 to 8.4; oxalate and pyrophosphate Al from 0 to 1.17%, and 0.02 to 0.58%, respectively; and oxalate and pyrophosphate Fe from 0.02 to 2.25% and 0 to 1.28%, respectively; PSI (P sorption index) values varied between 0 and 55.1. The Mehlich‐3 Al values ranged from 24 to 2600 mg kg‐1. A close relationship was observed between Mehlich‐3 and oxalate Al values (r=0.77), although the regression line tended to be curvilinear. Mehlich‐3 Al was better correlated than oxalate Al to pyrophosphate Al (r=0.66 vs. r=0.59) and also to pH‐NaF (r=0.89 vs. r=0.74). The Mehlich‐3 Al is almost as good as oxalate Al in estimating non‐crystalline Al, the correlation coefficients between log PSI and log (Mehlich‐3 Al) or log (oxalate Al) being 0.51 and 0.57, respectively. The Mehlich‐3 Fe correlated to available (r=0.63), exchangeable (r=0.65) and soluble Fe (r=0.66), but not to non‐crystalline Fe.  相似文献   

14.
Abstract

Twenty surface soil samples, representing two major soil orders alfisols and vertisols were extracted with 0.01N Na2 EDTA solution (pH 4.8) at a soil/solution ratio of 1:25. Phosphorus in the extract was determined following ammonium molybdate‐stannous chloride colorimetric method. The EDTA extractable P showed significant positive correlations with extractable P according to the Olsen, Morgan, Bray 1 and 2 and also with inorganic phosphorus fractions associated with Al, Ca and Fe.  相似文献   

15.
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 (Alp) 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.  相似文献   

16.
Minerals with large specific surface areas promote the stabilization of soil organic matter (SOM). We analysed three acidic soils (dystric, skeletic Leptic Cambisol; dystric, laxic Leptic Cambisol; skeletic Leptic Entic Podzol) under Norway spruce (Picea abies) forest with different mineral compositions to determine the effects of soil type on carbon (C) stabilization in soil. The relationship between the amount and chemical composition of soil organic matter (SOM), clay content, oxalate‐extractable Fe and Al (Feo; Alo), and dithionite‐extractable Fe (Fed) before and after treatment with 10% hydrofluoric acid (HF) in topsoil and subsoil horizons was analysed. Radiocarbon age, 13C CPMAS NMR spectra, lignin phenol content and neutral sugar content in the soils before and after HF‐treatment were determined and compared for bulk soil samples and particle size separates. Changes in the chemical composition of SOM after HF‐treatment were small for the A‐horizons. In contrast, for B‐horizons, HF‐soluble (mineral‐associated) and HF‐resistant (non‐mineral‐associated) SOM showed systematic differences in functional C groups. The non‐mineral associated SOM in the B‐horizons was significantly depleted in microbially‐derived sugars, and the contribution of O/N‐alkyl C to total organic C was less after HF‐treatment. The radiocarbon age of the mineral‐associated SOM was younger than that of the HF‐resistant SOM in subsoil horizons with small amounts of oxalate‐extractable Al and Fe. However, in horizons with large amounts of oxalate‐extractable Al and Fe the HF‐soluble SOM was considerably older than the HF‐resistant SOM. In acid subsoils a specific fraction of the organic C pool (O/N‐alkyl C; microbially‐derived sugars) is preferentially stabilized by association with Fe and Al minerals. Stabilization of SOM with the mineral matrix in soils with large amounts of oxalate‐extractable Alo and Feo results in a particularly stable and relatively old C pool, which is potentially stable for thousands of years.  相似文献   

17.
Abstract

In nineteen surface horizons of red Mediterranean soils from various locations of Greece, phosphorus (P) sorption experiments were conducted and the sorption characteristics were studied in relation to soil properties. Phosphate sorption data were fitted both to the Langmuir and Freundlich equations. From these equations, the following P sorption parameters were determined from the Freundlich equation, X = ACn, the parameters A (the phosphate sorbed at C = 1 mg P/L), n (the P sorption intensity), the P sorption index (PS = X/log C) and maximum P sorption (Xmfr). From the Langmuir equation, C/X = 1/KXm + C/Xm, the parameters K (showing the bonding energy), maximum P sorption (Xmla), the quantity of P adsorbed at a standard concentration of 0.2 mg P/L (P0.2), and P maximum buffering capacity (PMBC). The Freundlich parameter A was strongly correlated to the clay and sesquioxides ("free”; iron and aluminum oxides and amorphous iron oxides) content. Seventy‐four percent of the variance of this parameter was explained by clay and “free”; iron (Fe) content. The Freundlich parameter n was significantly correlated with pH and amorphous iron oxides content, while 52% of its variance was explained by amorphous Fe and dithionite extrac‐table aluminum (Al). The P sorption maxima calculated from the Freundlich equation were in general lower than those calculated by the Langmuir equation. Both these parameters were strongly correlated with clay and more slightly with sesquioxides content. About 50% of their variance was explained by clay content of the soils. The P sorption index was strongly correlated with the clay content and less strongly with dithionite‐extractable Fe and Al. The P‐buffering capacity calculated from the data of Langmuir equation was also strongly correlated with these two parameters. In addition, clay content and dithionite‐extractable Fe and Al were well correlated to the amounts of P required to obtain an equilibrium concentration of 0.2 mg P/L while 61% of the variation of this parameter was explained by the clay and the dithionite‐extractable Fe content. From these findings, it seems that for the red Mediterranean soils from Greece, P sorption is affected by clay content and iron and aluminum oxide contents.  相似文献   

18.
《Geoderma》1986,37(2):137-147
P sorption curves (18 hours, 0.01 M CaCl2) were determined for various A, AB, B and C horizons of six Andepts. Two of these soils were formed in alluvially sorted and redeposited volcanic ash. P buffer capacity (PBC) and equilibrium solution P concentration (EPC) were derived from the curves. PBC was high for all samples indicating large sorption capacities. Soils formed in alluvial ash had lower PBC than those developed in airfall ash. In the latter soils, PBC was affected by degree of weathering. Multiple regression indicated that most variation in PBC was accounted for by citrate-dithionite minus pyrophosphate extractable Al, oxalate minus pyrophosphate extractable Al, and pyrophosphate extractable Fe. This suggests that allophane, crystalline and non-crystalline aluminium hydrous oxides, and Fe associated with organic matter, account for the predominant P-sorbing sites. The low EPC figures, which were correlated with Olsen extractable P, indicate potential P deficiency as a limitation to crop production.  相似文献   

19.
The geochemical processes influencing iron and aluminium mobilization and immobilization processes in mine soils are discussed. The study was carried out on 11 soils from the As Pontes mine dump, in the process of reclamation. The soils differ in age, spoils nature, reclamation tasks and type of vegetation, covering a wide range of physico-chemical conditions. Oxalate and pyrophosphate extractable Al and Fe (Alo, Alp, Feo, Fep), and dithionite extractable Fe (Fed) were analysed. These fractions were related to the solution Al and Fe forms and contents and to other soil properties (Eh, pH, sulfides, organic matter, cation exchange capacity, and composition of the soil solution). Alo ranged between 2.2 and 111.2 cmolc kg-1; 5 to 80% of this Alo was organic aluminium (Alp). Fed ranged between 8.5 and 215.6 cmolc kg-1; 20 to 70% was poorly-criystalline iron (Feo). The solution concentrations of Al and Fe ranged between <0.1 and 319.2, and between <0.1 and 46.7 mg L-1, respectively. The results showed that the spoil nature (mostly carbonaceous clays and slates differing in sulfide content) and the reclamation tasks undertaken (topsoiling, liming with fly ash) determine the forms and contents of Al and Fe in the solid phase as well as in the soil solution and also its distribution between the solid and liquid phases.  相似文献   

20.
Abstract

Paper birch and hybrid poplar were grown in acid minesoils amended with different rates and types of lime. Growth of the trees was correlated with soil pH, Ca, Mg, K, P and three measures of extractable Al ‐ 1 N KCl, 0.01 M CaCl2 and H2O extractable Al. Correlations between soil pH and extractable Al and between the three measures of extractable Al were also determined. Soil pH accounted for the largest share of the total variation in root and shoot growth of both species over all soils. Correlations between tree growth and extractable Al for all soils combined were low and generally non‐significant. Significant correlations were obtained between soil pH and extractable Al and between the three measures of extractable Al, however, the relationships varied among soils.  相似文献   

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