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1.
Abstract

Twelve soils with low‐medium phosphorus (P) retention capacities were equilibrated for 3 months with soluble phosphate at a rate of 100 mg P kg‐1 soil. The P sorption properties of these soils both with and without added P were studied, including equilibrium P concentration (EPCo), standard P requirement (SPR), soil P sorption capacity (b), maximum buffer capacity (MBC), and P sorption index (P‐SI). In general, the soils with no added P showed low values of all the above parameters. Oxalate extractable aluminum appeared to be the major responsible element for the control of P sorption in these soils. The addition of P to these soils had a considerable effect on their P sorption properties. The changes in EPCo were well correlated with P sorption index (r=0.80; p≤0.01 ). The EPCo values of the soils with and without added P were closely correlated to bicarbonate extractable P (P0lsen) and calcium chloride extractable P (PCaC12), with r=0.80, and r=0.99 (p≤0.001), respectively. Ninety percent of the variability in EPCo was explained by the corresponding variability in POlsen when a curvilinear relationship was adopted. The P sorption properties examined appear to be useful parameters to assess the environmental impact of soil P on the quality of surface waters.  相似文献   

2.
Abstract

Poor accessibility and cost of soil testing reduce effectiveness of fertilizer use on small‐scale subsistence farms, and inadequate funding promotes adoption of soil tests in developing countries with minimal validation. For example, Mehlich I extraction of phosphorus (P) currently used extensively in Guatemala may not be suitable for Guatemala's broad range of soils. At least four alternatives are available but relatively untested [Bray 1, Mehlich III, Olsen, and pressurized hot water (PHW)]. Pressurized hot water is relatively simple and inexpensive but is not yet tested against other extraction methods under variable P or potassium (K) fertilization levels. To determine whether PHW‐extracted nutrients could be used to predict maize yield and nutrient concentration and uptake, soil, plant tissue and grain samples were obtained from a multiple‐site field study, and calibration studies were conducted using five rates of P and three rates of K on soils incubated without plants or cropped with maize in greenhouse and field conditions. In the multiple‐site field study, maize yield related significantly to PHW‐extractable P (r2=0.36) and to leaf P concentration (r2=0.23), but Mehlich I–extractable P did not. In the two soils used in the greenhouse study, maize yield, vegetative P concentration, and total P uptake by maize were predicted by PHW‐extractable P (R2=0.72, 0.75, and 0.90, respectively). In the field experiment, grain yield was not improved by P or K application, but P concentration of maize leaf tissue did relate significantly with PHW‐extracted P (R2=0.40). Mehlich I did not. There were no yield responses to K application in any experiment, but relationships defined between extractable K for all five K‐extraction procedures and soil‐applied K were similarly significant. In comparison, PHW was as good as or better than Olsen whereas Bray 1 and Mehlich III were less consistent. Mehlich I was overall the poorest P extractant. Mehlich I extraction of P should be replaced by one of the four alternatives tested. PHW is the least expensive and, therefore, most viable for use in Guatemala soils.  相似文献   

3.
Abstract

Investigating the relation between concentration or release of phosphorus (P) into soil solution (CaCl2‐P, determined by 0.01 M CaCl2 extraction of soils) and soil test phosphorus (Olsen P, or 0.5 N NaHCO3‐extractable soil phosphorus) for 10 widely ranging and variously managed soils from central Italy, a change point was evident where the slopes of two linear relationships meet. In other words, it was possible to distinguish two sections of the plots of CaCl2‐P against Olsen P, for which increases of CaCl2‐P per unit of soil test P increase were significantly (p<0.05) greater above than below these change points. Values of change point ranged from 14.8 to 253.1 mg kg?1 Olsen P and were very closely correlated (p<0.001) to phosphorus sorption capacity of soils. Similar change points were also previously observed when Olsen P (and also Mehlich 3 P) of surface soils was related to the P concentration of surface runoff and subsurface drainage. Because insufficient data are available relating P in surface soils and amount of P loss by overland, subsurface, or drainage flow, using the CaCl2 extraction of soil can be convenient to determine a change point in soil test P, which may be used in support of agricultural and environmental P management.  相似文献   

4.
Abstract

Changes in agronomic and environmental soil phosphorus (P) availability parameters, i.e., Mehlich‐ and Olsen‐extractable P, reversibly‐adsorbed P, soil‐solution P, and equilibrium‐P concentration were determined following equilibration of 13 Italian soils with five rates of P application (0, 12.5, 25, 50, and 100 mg P kg‐1 soil). Soil P availability as determined by each parameter increased with added P. The relative change in soil P availability with added P was a function of soil sorption index silicon (SI), according to the equation DP=(Padded)a*exp(b+g*SI). This equation accounted for 94 to 98% of the variance in soil‐P availability. The inclusion of SI in a soil testing program may increase the reliability in assessing both soil‐P fertilizer requirements and the vulnerability of a soil to P loss in runoff following land application of fertilizer or manure P.  相似文献   

5.
Abstract

A study was undertaken to evaluate the agreement among different university laboratories performing the Olsen, Bray P1, and Mehlich I tests for P on a diverse group of noncalcareous agricultural soils and to develop relationships among the Olsen, Bray P1, Mehlich I, and Mehlich III soil tests. For each test, the results from the individual laboratories were highly correlated (r2 0.90) and in almost all instances the slopes of the equations describing the relationships among laboratories approached one, The results indicate that the Olsen, Bray P1 and Mehlich I soil tests may be performed with a high degree of precision when standard soil test procedures are followed.

Of the three most commonly performed tests in the U.S. (Olsen, Bray P1, and Mehlich I), the Olsen and Mehlich I tests were the most highly correlated (r2 = 0.87) although the Mehlich I test removed approximately one and one half times more P than did the Olsen test. Bray P1 and Olsen and Mehlich I P were less highly correlated (r2 ≤ 0.72) and the relationships between these variables were influenced by the texture of the soils. The quantity of P removed by the Bray P1 test was on the order of two and three times greater than that removed by the Olsen and Mehlich I tests, respectively. The Bray P1 and Mehlich III soil tests were highly correlated (r2 = 0.97) and similar quantities of P were extracted from the soil by the two tests.  相似文献   

6.
Abstract

Optimum crop production depends, among other things, on the maintenance of adequate plant nutrients in the root zone. The objective of this study was to find a reliable index for assessing needs for supplemental phosphorus (P) in soils of Morogoro District, Tanzania. Six indices of P availability, namely: Bray and Kurtz No. 1 (BK1), Bray and KurtzNo.2 (BK2), Mehlich 1, Mehlich 3, Olsen and ammonium bicarbonate‐DTPA (AB‐DTPA), were evaluated. Evaluation of the P indices involved relating extractable P contents by different methods with crop response data expressed as relative yields. The response data was obtained from pot trials with soil samples from ten repesentative soils designated as benchmark soils of the district. Treatments were absolute control, 0, 10, 20, and 30 mg P kg‐1 of soil. Correlation of maize relative yields with soil test values by the six indices of P availability resulted in correlation coefficients ranging from 0.65 to 0.90. The Olsen method gave the highest r value suggesting that it was superior to the others. However, using the Cate and Nelson approach, the Olsen and ammonium bicarbonate‐DTPA methods were found to be at par and superior to the others. They each accounted for 76% of the variations observed in maize relative yields, respectively. The critical P levels for the indices were 10.50 mg P kg‐1 for Olsen and 2.80 mg P kg‐1 for the AB‐DTPA method. Phosphorus fertility categories were delineated in relation to Olsen extractable P as: low (<6.50 mg P kg‐1), medium (6.50 to 23.0 mg P kg‐1), and high (>23.0 mg P kg‐1). Based on this classification it was determined that 16%, 25 %, and 59% of the surveyed area had low, medium, and high P levels, respectively. About 40% of the surveyed area may, therefore, require fertilization with P for optimum yields.  相似文献   

7.
Abstract

Water treatment residuals (WTR) can adsorb tremendous amounts of phosphorus (P). A soil that had biosolids applied eight times over 16 years at a rate of 6.7 Mg ha?1 y?1 contained 28 mg kg?1 ammonium–bicarbonate diethylenetriaminepentaacetic acid (AB‐DTPA), 57 mg kg?1 Olsen, 95 mg kg?1 Bray‐1, and 53 mg kg?1 Mehlich‐III extractable P. To 10 g of soil, WTRs were added at rates of 0, 0.1, 1, 2, 4, 6, 8, and 10 g, then 20 mL of distilled deionized H20 (DI) were added and the mixtures were shaken for 1 week, filtered, and analyzed for soluble (ortho‐P) and total soluble P. The soil–WTR mixtures were dried and P extracted using DI, AB‐DTPA, Olsen, Bray‐1, and Mehlich‐III. Results indicated that all methods except AB‐DTPA showed reduced extractable‐P concentrations with increasing WTR. The AB‐DTPA extractable P increased with increasing WTR rate. The water‐extractable method predicted P reduction best, followed by Bray‐1 and Mehlich‐III, and finally Olsen.  相似文献   

8.
Soil testing is widely adopted as an essential diagnostic tool for identifying soil nutrient factors that limit sustained crop production. A systematic approach for rapid soil testing and fertilizer recommendation has been introduced and widely used in China by Agro Services International (ASI), USA. To verify the usefulness and reliability of the ASI method in soil testing and fertilizer recommendation in comparison with other commonly used traditional soil testing methods, 294 soil samples from major agricultural regions and soil types in China with a wide range of soil pH, from 5.1 to 8.9, were taken and analyzed for available phosphorus (P) and potassium (K) by the ASI multielement extraction solution and selected traditional methods, Olsen extractant for P, ammonium acetate (NH4OAc) extractant for K, and multielement extractant Mehlich 3 for P and K. Also, 46 soils were selected from northern China regions for a greenhouse trial with sorghum seedlings to determine if the soil testing values correlate well with plant response. Results indicated that the amount of soil P extracted by the ASI method (ASI P) was correlated to both soil extractable P tested by the Olsen extractant (Olsen P) and Mehlich 3 extractant (Mehlich 3 P). The correlation coefficient of ASI P with Mehlich 3 P (R2 = 0.86) was greater than that of ASI P with Olsen P (R2 = 0.74) across all selected soils. A good correlation was also found between the exchangeable K from the ASI method with the traditional ammonium acetate method (R2 = 0.81) and the Mehlich 3 method (R2 = 0.85). The results from the greenhouse trial showed that the extractable P and exchangeable K by the ASI multielement extraction solution could be used to represent the fertility status of soil P and K for the selected soils. Regression analysis indicated that the relative dry-matter yield of the sorghum plants can be predicted with either ASI P and ASI K values with the correlation coefficients (R2) values of 0.78 and 0.72 respectively and could be a good measure for soil testing and fertilizer recommendation in the selected soils and regions in China.  相似文献   

9.
Abstract

Soil phosphorus (P) extractants are often selected according to the correlation or regression between test values and crop performance (e.g., P uptake and/ or yield). Although this criterion is an essential determinant of extractant performance, it is often inadequate for evaluating whether extractants accurately discriminate between P‐deficient and P‐sufficient soils, or whether they produce reliable critical level estimates or repeatable soil P measurements. Four supplementary indices were evaluated that may provide a more direct assessment of extractant performance. The potential use and reliability of the indices were investigated in an evaluation of four soil P extractants, Modified Truog, Mehlich 3, Olsen, and ion‐exchange resin, using data from a greenhouse experiment. Coefficients of determination between relative dry matter yield and extractable P failed to identify differences among the extractants, ranging from 0.95 to 0.97. Coefficients of determination between extractable P and P added ranged from 0.96 to 0.97 except for one method at 0.83. The proposed indices, however, produced a ranking of the extractants related to their performance. The Kappa efficiency (K EFF) index indicated that Mehlich 3 provided better detection of P‐sufficient and P‐deficient soils than either Olsen or Truog (K FFF values of 0.92, 0.83, and 0.68, respectively). These index values reflect that the extradants correctly detected P deficiency in 17 of 18, 17 of 18, and 15 of 18 soils. The slight superiority of Mehlich 3 over Olsen was due to its correct detection of 9 of 9 P‐sufficient soils while the Olsen and Truog extradants correctly detected 8 of 9 P‐sufficient soils. Further studies are needed, especially field studies, to determine whether these indices accurately reflect the reliability of the extradants for use in diagnosis and recommendation. Because these indices directly assess success in identifying deficient and sufficient conditions, their use in extractant evaluations should provide more specific, purposeful evaluations than methods based solely on correlation and regression.  相似文献   

10.
Abstract

Phosphorus extractants have not been tested extensively in the Southeast. An experiment was carried out to compare four P extractant methods using samples from a field P‐K factorial experiment with soybeans (Glycine max (L.) Merr.) at three locations in Georgia over four years. There were five P rates ranging from none to 80 kg ha‐1. Soils and plant tissue were sampled at mid‐summer and yields were recorded. The four P extractants compared were Olsen, Mehlich 1, Mehlich 2, and Bray 1. Quadratic regressions for soil P versus plant P and P rates were not significant compared to linear regressions. There were no significant yield responses to P. All extractants except Olsen were similar in their response to added fertilizer P as measured by linear r2 values. Olsen P gave lower linear r2 values both with P rate and with plant P. Mehlich 1 values were highly correlated with Mehlich 2 (0.94**) and Bray 1 (0.96**). Mehlich 2 and Bray 1 gave nearly the same soil P values with linear regressions of slope of 1.0 and low intercepts. Results from these experiments show that Mehlich 1, Mehlich 2, or Bray 1 could be used successfully on these soils, but that Olsen should be avoided.  相似文献   

11.
Abstract

A new soil extractant (H3A) with the ability to extract NH4, NO3, and P from soil was developed and tested against 32 soils, which varied greatly in clay content, organic carbon (C), and soil pH. The extractant (H3A) eliminates the need for separate phosphorus (P) extractants for acid and calcareous soils and maintains the extract pH, on average, within one unit of the soil pH. The extractant is composed of organic root exudates, lithium citrate, and two synthetic chelators (DTPA, EDTA). The new soil extractant was tested against Mehlich 3, Olsen, and water for extractable P, and 1 M KCl and water‐extractable NH4 and NO2/NO3. The pH of the extractant after adding soil, shaking, and filtration was measured for each soil sample (5 extractants×2 reps×32 soils=320 samples) and was shown to be highly influential on extractable P but has no effect on extractable NH4 or NO2/NO3. H3A was highly correlated with soil‐extractable inorganic N (NH4, NO2/NO3) from both water (r=0.98) and 1 M KCl (r=0.97), as well as being significantly correlated with water (r=0.71), Mehlich 3 (r=0.83), and Olsen (r=0.84) for extractable P.  相似文献   

12.
Phosphorus (P) is an essential nutrient for plant growth and reproduction. One of the tasks of soil testing is to identify whether the soil P level is sufficient to meet crop requirements, and if not, to provide an estimate of the quantity of P that must be added for good growth of a given crop. Data for 12 soils (11 series) from Hawaii were used to develop correlations between critical P concentrations in soil solution derived from P sorption isotherms with P extracted with Mehlich 3, Olsen, or modified Truog solutions. Extractable P, in turn, was correlated with P fertilizer requirements. Critical P levels in soil solution reported in the literature for various crops ranged from 0.005 mg L?1 for cassava (Manihot esculenta) to 0.30 for lettuce (Lactuca sativa) and to 1.6 for nonmycorrhizal onions (Allium cepa). The P buffer coefficient, defined as the ratio of fertilizer P added to extractable P, averaged 2.2, 4.2, and 8.6 for the modified Truog, Olsen, and Mehlich 3, respectively. Phosphorus requirements for certain crops could be estimated by the following steps: (i) obtaining (possibly one time only) soil solution P levels via P sorption isotherm for a given soil (series or family), (ii) identifying the critical soil solution P for a given crop from the literature, (iii) regressing soil solution P against extractable P, and (iv) establishing relationships between extractable P and fertilizer P.  相似文献   

13.
Abstract

Soil nutrient extraction methods, which are currently being used in Malawi, are time consuming and require too many resources. The use of a universal soil extractant would greatly reduce resource requirements. The objectives of the study were to (i) compare the universal soil extractants, Mehlich 3 (M3) and Modified Olsen (MO) with ammonium acetate (AA), Bray P1 (BPl), and diethylene triamine penta acetic acid (DTPA) in the amount of nutrients extracted, (ii) determine the relationship among the extractants for the nutrients they extract, and (iii) determine the critical soil‐test levels of phosphorus (P), potassium (K), and zinc (Zn) for a maize crop. Missing nutrient trials involving P, K, and Zn were conducted on thirty sites across Malawi using maize (Zea mays L.). Phosphorus application rates ranged from 40 to 207 kg P2O5 ha‐1. Potassium and Zn were applied at 75 kg K2O and 10 kg Zn ha‐1, respectively. Procedures of Cate and Nelson were used to identify soil nutrient critical levels. Results showed that the correlations between M3 and BP1, and MO and BPl were highly significant (r=0.93, 0.94, respectively). Mehlich 3 extractable K and AA extractable K (r=0.90), MO and AA extractable K (r=0.94) were highly significant (P<0.01) and the correlations between M3 and AA and MO and AA extractable calcium (Ca) (r=0.92, 0.90, and 0.94, respectively) were also highly significant (P<0.01). The correlations between M3, MO, and AA extractable magnesium (Mg) (r=0.99) were highly significant (P<0.01). Zinc, copper (Cu), and manganese (Mn) extracted with M3 and DTPA were significantly correlated (r=0.89, 0.87, and 0.95, respectively). Correlations between MO and DTPA extractable Zn, Cu, and Mn were also highly correlated (r=0.89,0.85, and 0.95, respectively). Maize grain yields ranged from 730 to 9,400 kg ha‐1. Mehlich 3‐P and MO‐P critical levels were 31.5 and 28.0 μg g‐1, respectively. Mehlich 3 and MO gave a similar critical level of 0.2 cmol kg‐1 for K while Zn critical levels were 2.5, and 0.8 μg g‐1 for M3 and MO, respectively. Mehlich 3 and MO were equally effective in separating responsive to none responsive soils for maize in Malawi.  相似文献   

14.
Abstract

Knowledge of the change in soil extractable phosphorus (P) as a consequence of soil P fertilization could be useful in discriminating soils with a potential for soil P release to runoff or movement of P along the soil profile. In this research, soils with low to medium P retention capacity were equilibrated for 90 days with soluble P (KH2PO4) at rate of 100 mg P kg‐1 soil. After this period, soil samples both with and without the P addition were analyzed using six conventional methods: 1) Olsen, 2) Bray 1,3) Mehlich3,4) Egner, 5) Houba, dilute CaCl2 solution, and 6) distilled water, and three “innovative”; P‐sink methodologies: 1) Fe oxide‐coated paper strip, 2) anion exchange resin membrane, and 3) cation‐anion exchange resin membrane. The soils without P addition had low levels of extracted P as determined by all nine procedures. Net increases in the amount of P extracted from the soils with added P ranged from 4.2 mg kg‐1 (CaCl2 extraction) to 57.6 mg kg‐1 (cation‐anion resin membrane extraction). Relationships between change in extracted P and i) physical and chemical characteristics, and ii) soil P sorption properties are also presented and discussed.  相似文献   

15.
Accumulation of surplus phosphorus (P) in the soil and the resulting increased transport of P in land runoff contribute to freshwater eutrophication. The effects of increasing soil P (19–194 mg Olsen‐P (OP) kg−1) on the concentrations of particulate P (PP), and sorption properties (Qmax, k and EPCo) of suspended solids (SS) in overland flow from 15 unreplicated field plots established on a dispersive arable soil were measured over three monitoring periods under natural rainfall. Concentrations of PP in plot runoff increased linearly at a rate of 2.6 μg litre−1 per mg OP kg−1 of soil, but this rate was approximately 50% of the rate of increase in dissolved P (< 0.45 μm). Concentrations of SS in runoff were similar across all plots and contained a greater P sorption capacity (mean + 57%) than the soil because of enrichment with fine silt and clay (0.45–20 μm). As soil P increased, the P enrichment ratio of the SS declined exponentially, and the values of P saturation (Psat; 15–42%) and equilibrium P concentration (EPCo; 0.7–5.5 mg litre−1) in the SS fell within narrower ranges compared with the soils (6–74% and 0.1–10 mg litre−1, respectively). When OP was < 100 mg kg−1, Psat and EPCo values in the SS were smaller than those in the soil and vice‐versa, suggesting that eroding particles from soils with both average and high P fertility would release P on entering the local (Rosemaund) stream. Increasing soil OP from average to high P fertility increased the P content of the SS by approximately 10%, but had no significant (P > 0.05) effect on the Psat, or EPCo, of the SS. Management options to reduce soil P status as a means of reducing P losses in land runoff and minimizing eutrophication risk may therefore have more limited effect than is currently assumed in catchment management.  相似文献   

16.
Abstract

Soil test recommendations currently used in Alaska are based on a limited amount of in‐state data along with consideration of data from other states. Recently, Mehlich 3 extractable P has been found to be highly correlated to yield on representative agricultural soils in Alaska. To fully use its multi‐element capability, a study was conducted to correlate Mehlich 3 extractable P and cations (K, Ca, and Mg) with the P and cations extracted by the Bray 1 and ammonium acetate methods respectively.

When Mehlich 3 extractable K and Mg were regressed with ammonium acetate extractable K and Mg respectively, the relationship was essentially one‐to‐one and the relationship held across all soils tested. Significant variation was observed among soils in the extraction of Mehlich 3‐P and Ca relative to Bray 1‐P and ammonium acetate‐Ca. Individual soil character appeared to affect the regressions for extractable P and Ca, even though the R2 values were generally high. The regression slopes for Mehlich 3‐P versus Bray 1‐P ranged from 1.01 to 1.88 with Mehlich 3 extracting an average of 66% more P than Bray 1 in the volcanic ash soils, and 12% more in the loess soils. The regression slopes for Mehlich 3‐Ca versus ammonium acetate‐Ca ranged from 0.95 to 1.33, and the former extracted an average of 17% more Ca than the latter. It is suggested that the regression data of P and Ca can be extrapolated to other soils based on soil classification; to extend the soil test data over a geographic base.  相似文献   

17.
Abstract

Various soil tests are used to estimate phosphorus (P) availability for both crop uptake and potential loss to water. Conversion equations may provide a basis for comparison between different tests and regions, although the extent to which information can be interchanged is uncertain. The objective was to determine and quantify relationships between specific soil test extractants for samples taken annually in October and February over 4 years from four sites in each of eight soil series under grassland. The extractants comprised Mehlich‐3, Morgan, Olsen, Bray‐1, lactate–acetate, CaCl2 (1∶2 and 1∶10 soil–solution ratios), and resin. The results showed distinct relationships for each soil series, for which individual lines regression models (different intercepts and slopes) were superior to a single conversion equation across all soils. The ensuing difference between soils was large and ranged from 1.9 to 8.0 and 9.2 to 15.6 mg kg?1 P for Morgan and Olsen, respectively, at 20 mg kg?1 Mehlich‐3 P. Generally, the environmentally oriented tests CaCl2 and resin correlated best with Morgan. Some soil‐specific limitations were also observed. CaCl2 was less efficient than Morgan, and Morgan less efficient than Mehlich‐3 on a high Fe–P soil derived from Ordovician‐shale diamicton, compared with the general trend for other soils. This finding suggests that further disparity may arise where evaluation of critical, or other, limits across regions involves even a limited sequence of tests.  相似文献   

18.
Abstract

Soil analysis for small farms in developing countries is often inconvenient and prohibitively expensive, yet the information gained from these soil tests could result in significant benefits. Based on tests done on a limited range of soils, the pressurized hot water (PHW) extraction coupled with colorimetric or turbidimetric analysis is a promising alternative. Before this extraction and analysis can be used in developing countries, testing is needed across the range of soils found in these countries. At Brigham Young University (BYU), 228 soils from Guatemala and Morocco were analyzed for NO3‐N, phosphorus (P), and potassium (K) using standard methods (water–CTA, Olsen–molybdic acid and ammonium acetate–atomic absorption, respectively). Results were correlated to values obtained from the PHW extraction coupled with colorimetric or turbidimetric analytical procedures. The relationships between these tests were good (r2 values of 0.96, 0.71, and 0.52 for NO3‐N, P, and K, respectively). In an additional study comparing several P extraction methods for Guatemala soils, relationships between PHW‐extractable P and Olsen‐, Bray I–, and Mehlich I–extractable P (r2 values of 0.75, 0.67, and 0.46, respectively) suggest that PHW is a promising P‐extraction procedure for use in Guatemala. Overall, PHW extraction and accompanying analyses are a less expensive alternative to current soil nutrient extraction and analysis procedures for the soils of Morocco and Guatemala.  相似文献   

19.
Evaluation of five soil phosphorus (P) extractants was done on southwestern Nigerian soils from sedimentary and basement complex parent materials to determine the relationship between the extractants and the most appropriate extractant for the soils. The soils differed in properties. Generally, soils from the basement material had less available P compared with sedimentary material. Olsen extracted the greatest P. Bray 1 measured 67% of Olsen P, Hunter measured 52%, Mehlich measured 42%, and Ambic measured 24%. Positive and significant regression (P < 0.001) existed among Bray 1, Olsen, Mehlich, Hunter, and Ambic extractants. The strongest relationship was found among Olsen, Mehlich, and Ambic P. The relationship between maize P uptake and extracted P was quadratic, whereas the relationship with Mehlich was logarithmic. Bray, Mehlich, and Olsen P were the significant contributors to the maize P uptake and dry-matter yield. Extractants in order of P extraction were Olsen > Bray 1 > Hunter > Mehlich > Ambic.  相似文献   

20.
Abstract

Phosphorus fertilizer recommendations were compared by interpretations from P isotherms, Olsen extractable P and the Mitscherlich‐Bray model based on the Olsen method for 15 soils from the Chaouia (dryland) region of Morocco. The P isotherms were fit to straight line and second degree polynomial equations. The P buffer indexes (PBI) derived from the isotherms were not significantly correlated to P buffer capacities as measured by a single P buffer capacity index, but negatively correlated to Olsen P (r = ‐0.63), relative yield (r = ‐0.76) and P uptake (r = ‐0.66). Phosphorus in solution was a quadratic function of P added in 0.01 M CaCl2equilibrium solution. The P fertilizer recommendations to maintain soil solution P concentrations at 0.01, 0.12 and 0.20 mg P L‐1were higher than recommended by direct interpretation of plant response to Olsen extractable P and the quantity based on the Mitscherlich‐Bray model as calculated from Olsen available P values. The P fertilizer recommended to maintain soil solution P of 0.10 mg P L‐1was significantly correlated with Olsen P (r = 0.71) as was that recommended Mitscherlich‐Bray log transformation model (r = 0.81), and nonlinear least square estimation (r = 0.78). Field research will be needed to evaluate if the P fertilizer recommended to maintain this solution P concentration is adequate for maximum economic wheat grain yield under field conditions  相似文献   

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