Spatial analysis of phosphorus sorption capacity in a semiarid altered wetland

The observed increase in phosphorus (P) loading into the Jordan River could increase eutrophication processes in Lake Kinneret, the only freshwater lake in Israel, which provides 25% of the country's drinking water. The P may originate from the peat soils of the highly altered Hula Valley's semiarid wetland ecosystem through which the Jordan River runs. The objectives of this research were to ascertain the sorption capacity of these soils and to identify areas with high potential for P release from soils to ground water. We extracted 80 soil samples collected across the valley with ammonium oxalate and determined the ratio of extractable P to Fe and Al, from which we derived the degree of phosphorus saturation (DPS). A relatively low DPS (<15%) was observed in Histosols compared with the high DPS (>30%) observed in many of the hydromorphic organo-mineral soils. We used a sequential Gaussian simulation technique to assess the spatial pattern of the DPS and found that the Histosols have a low probability (<10%) of exceeding the widely used environmental DPS threshold of 25%. The areas characterized by mineral soils, such as hydromorphic Vertisols and various marl redoximorphic soils, have a high probability (>60%) of exceeding the threshold value. The ability to predict the concentrations of dissolved P in ground water based on DPS values was somewhat impaired because of the preferential flow characteristics in this altered wetland.     

Is colloid-facilitated phosphorus leaching triggered by phosphorus accumulation in sandy soils?

The leaching of colloidal phosphorus (P(coll)) contributes to P losses from agricultural soils. In an irrigation experiment with undisturbed soil columns, we investigated whether the accumulation of P in soils due to excess P additions enhances the leaching of colloids and P(coll) from sandy soils. Furthermore, we hypothesized that large concentrations of P(coll) occur at the onset of leaching events and that P(coll) mobilized from topsoils is retained in subsoils. Soil columns of different P saturation and depth (0-25 and 0-40 cm) were collected at a former disposal site for liquid manure and at the Thyrow fertilization experiment in northeastern Germany. Concentrations of total dissolved P, P(coll), Fe(coll), Al(coll), optical density, zeta potential, pH, and electrical conductivity of the leachates were determined. Colloidal P concentrations ranged from 0.46 to 10 micromol L(-1) and contributed between 1 and 37% to total P leaching. Large P(coll) concentrations leached from the P-rich soil of the manure disposal site were rather related to a large P-content of colloids than to the mobilization of additional colloids. Concentrations of colloids and P(coll) in leachates from P-poor and P-rich columns from Thyrow did not differ significantly. In contrast, accumulation of P in the Werbellin and the Thyrow soil consistently increased dissolved P concentrations to maximum values as high as 300 micromol L(-1). We observed no first-flush of colloids and P(coll) at the beginning of the leaching event. Concentrations of P(coll) leached from 40-cm soil columns were not smaller than those leached from 25-cm columns. Our results illustrate that an accumulation of P in sandy soils does not necessarily lead to an enhanced leaching of colloids and P(coll), because a multitude of factors independent from the P status of soils control the mobility of colloids. In contrast, P accumulation generally increases dissolved P concentrations in noncalcareous soils due to the saturation of the P sorption capacity. This indicates that leaching of dissolved P might be a more widespread environmental problem in areas with P-saturated sandy soils than leaching of P(coll).     

Estimating dissolved reactive phosphorus concentration in surface runoff water from major Ontario soils

Phosphorus (P) loss from agricultural land in surface runoff can contribute to eutrophication of surface water. This study was conducted to evaluate a range of environmental and agronomic soil P tests as indicators of potential soil surface runoff dissolved reactive P (DRP) losses from Ontario soils. The soil samples (0- to 20-cm depth) were collected from six soil series in Ontario, with 10 sites each to provide a wide range of soil test P (STP) values. Rainfall simulation studies were conducted following the USEPA National P Research Project protocol. The average DRP concentration (DRP30) in runoff water collected over 30 min after the start of runoff increased (p < 0.001) in either a linear or curvilinear manner with increases in levels of various STPs and estimates of degree of soil P saturation (DPS). Among the 16 measurements of STPs and DPSs assessed, DPS(M3) 2 (Mehlich-3 P/[Mehlich-3 Al + Fe]) (r2 = 0.90), DPS(M3)-3 (Mehlich-3 P/Mehlich-3 Al) (r2 = 0.89), and water-extractable P (WEP) (r2 = 0.89) had the strongest overall relationship with runoff DRP30 across all six soil series. The DPS(M3)-2 and DPS(M3)-3 were equally accurate in predicting runoff DRP30 loss. However, DPS(M3)-3 was preferred as its prediction of DRP30 was soil pH insensitive and simpler in analytical procedure, ifa DPS approach is adopted.     

Relationship between soil test phosphorus and phosphorus in runoff: effects of soil series variability

Phosphorus loss in runoff from agricultural fields has been identified as an important contributor to eutrophication. The objective of this research was to determine the relationship between phosphorus (P) in runoff from a benchmark soil (Cecil sandy loam; fine, kaolinitic, thermic Typic Kanhapludult) and Mehlich III-, deionized water-, and Fe(2)O(3)-extractable soil P, and degree of phosphorus saturation (DPS). Additionally, the value of including other soil properties in P loss prediction equations was evaluated. Simulated rainfall was applied (75 mm h(-1)) to 54 1-m(2) plots installed on six fields with different soil test phosphorus (STP) levels. Runoff was collected in its entirety for 30 min and analyzed for total P and dissolved reactive phosphorus (DRP). Soil samples were collected from 0- to 2-, 0- to 5-, and 0- to 10-cm depths. The strongest correlation for total P and DRP occurred with DPS (r(2) = 0.72). Normalizing DRP by runoff depth resulted in improved correlation with deionized water-extractable P for the 0- to 10-cm sampling depth (r(2) = 0.81). The STP levels were not different among sampling depths and analysis of the regression equations revealed that soil sampling depth had no effect on the relationship between STP and P in runoff. For all forms of P in runoff and STP measures, the relationship between STP and runoff P was much stronger when the data were split into groups based on the ratio of oxalate-extractable Fe to Al. For all forms of P in runoff and all STP methods, R(2) increased with the inclusion of oxalate-extractable Al and Fe in the regression equation. The results of this study indicate that inclusion of site-specific information about soil Al and Fe content can improve the relationship between STP and runoff P.     

Phosphorus saturation in spodosols impacted by manure

Significant amounts of phosphorus (P) accumulate in soils receiving animal manures that could eventually result in unacceptable concentrations of dissolved P loss through surface runoff or subsurface leaching. The degree of phosphorus saturation (DPS) relates a soil's extractable P to its P sorbing capacity, and is reportedly a predictor of the P likely to be mobilized from a system. A DPS value (DPS-1) was derived that expressed the percentage of Mehlich 1-extractable P to the sorbing capacity of a Spodosol (expressed as the sum of oxalate-extractable Fe and Al). Values of DPS-1 were determined in various horizons of soil in current and abandoned dairy systems in South Florida's Lake Okeechobee watershed to assess P release potential. Land use within the dairies was classified as highly impacted by cattle (intensive and holding), and minimally impacted by cattle (pasture, forage, or native) areas. The A and E horizon of soils in heavily manure-impacted intensive and holding areas for both active and abandoned dairies generally had higher DPS-1 values than the pasture, forage, and native area soils, which were minimally impacted by manure. Degree of P saturation was also calculated as a percentage of Mehlich 1-extractable P to the sum of Mehlich 1-extractable Fe and Al (DPS-2). Both DPS-1 and DPS-2 were shown to be significantly (P = 0.0001) related to water-extractable P for all soil horizons, suggesting that either index can be used as an indicator for P loss potential from a soil.     

Degree of phosphorus saturation thresholds in manure-amended soils of alberta

The risk of P losses from agricultural land to surface and ground water generally increases as the degree of soil P saturation increases. A single-point soil P sorption index (PSI) was validated with adsorption isotherm data for determination of the P sorption status of Alberta soils. Soil P thresholds (change points) were then examined for two agricultural soils after eight annual applications of different rates of cattle manure and for three agricultural soils after one application of different rates of cattle manure. Linear relationships were found between soil-test P (STP) levels up to 1000 mg kg(-1) and desorbed P in the five Alberta soils. Weak linear relationships were also found between STP and runoff dissolved reactive phosphorus (DRP) in three of these soils. Change points for the degree of P saturation (DPS) were detected in four of the five soils at 3 to 44% for water-extractable P (WEP) and at 11 to 51% for CaCl(2)-extractable P (CaCl(2)-P). Change points were not found for DPS or runoff DRP. Overall DPS thresholds for the five soils combined were 27% for WEP and 44% for CaCl(2)-P at a critical desorbable-P value of 1 mg L(-1). The corresponding STP levels (44 mg kg(-1) for WEP and 71 mg kg(-1) for CaCl(2)-P) are similar to agronomic thresholds for crops grown on Alberta soils. Soluble P losses in overland flow and leaching may be greater in soils with DPS values that exceed these thresholds than in soils with lower DPS values.     

Disturbance of water-extractable phosphorus determination by colloidal particles in a heavy clay soil from the Netherlands

Water extraction methods are widely used to extract phosphorus (P) from soils for both agronomic and environmental purposes. Both the presence of soil colloids in soil water filtrates, and the contribution of colloidal P to the molybdate-reactive phosphorus (MRP) concentration measured in these filtrates, are well documented. However, relatively little attention has been given to the direct disturbance by colloids of MRP measurement. The objective of this paper is to show this influence found for water extracts with a soil to solution ratio of 1:60 (v/v) (P(w)), obtained from a heavy clay soil in the Netherlands. Colloidal particles, which passed a 0.45-mum filter, caused a large overestimation of MRP. The low ionic strength of the P(w) filtrates (on average 0.64 mmol(c) L(-1)) probably caused soil dispersion and increased detachment of colloids from soil during extraction. After NaCl addition, followed by 0.45-mum filtration, MRP was on average 93% lower. This can be ascribed to flocculation of colloids and removal by filtration. A low ionic strength can thus lead to the direct disturbance by colloidal particles of MRP measurement in waters from soils sensitive to release of colloids.     

Relating soil phosphorus to dissolved phosphorus in runoff: a single extraction coefficient for water quality modeling

Phosphorus transport from agricultural soils contributes to eutrophication of fresh waters. Computer modeling can help identify agricultural areas with high potential P transport. Most models use a constant extraction coefficient (i.e., the slope of the linear regression between filterable reactive phosphorus [FRP] in runoff and soil P) to predict dissolved P release from soil to runoff, yet it is unclear how variations in soil properties, management practices, or hydrology affect extraction coefficients. We investigated published data from 17 studies that determined extraction coefficients using Mehlich-3 or Bray-1 soil P (mg kg(-1)), water-extractable soil P (mg kg(-1)), or soil P sorption saturation (%) as determined by ammonium oxalate extraction. Studies represented 31 soils with a variety of management conditions. Extraction coefficients from Mehlich-3 or Bray-1 soil P were not significantly different for 26 of 31 soils, with values ranging from 1.2 to 3.0. Extraction coefficients from water-extractable soil P were not significantly different for 17 of 20 soils, with values ranging from 6.0 to 18.3. The relationship between soil P sorption saturation and runoff FRP (microg L(-1)) was the same for all 10 soils investigated, exhibiting a split-line relationship where runoff FRP rapidly increased at P sorption saturation values greater than 12.5%. Overall, a single extraction coefficient (2.0 for Mehlich-3 P data, 11.2 for water-extractable P data, and a split-line relationship for P sorption saturation data) could be used in water quality models to approximate dissolved P release from soil to runoff for the majority of soil, hydrologic, or management conditions. A test for soil P sorption saturation may provide the most universal approximation, but only for noncalcareous soils.     

Soil testing to predict phosphorus leaching

Subsurface pathways can play an important role in agricultural phosphorus (P) losses that can decrease surface water quality. This study evaluated agronomic and environmental soil tests for predicting P losses in water leaching from undisturbed soils. Intact soil columns were collected for five soil types that a wide range in soil test P. The columns were leached with deionized water, the leachate analyzed for dissolved reactive phosphorus (DRP), and the soils analyzed for water-soluble phosphorus (WSP), 0.01 M CaCl2 P (CaCl2-P), iron-strip phosphorus (FeO-P), and Mehlich-1 and Mehlich-3 extractable P, Al, and Fe. The Mehlich-3 P saturation ratio (M3-PSR) was calculated as the molar ratio of Mehlich-3 extractable P/[Al + Fe]. Leachate DRP was frequently above concentrations associated with eutrophication. For the relationship between DRP in leachate and all of the soil tests used, a change point was determined, below which leachate DRP increased slowly per unit increase in soil test P, and above which leachate DRP increased rapidly. Environmental soil tests (WSP, CaCl2-P, and FeO-P) were slightly better at predicting leachate DRP than agronomic soil tests (Mehlich-1 P, Mehlich-3 P, and the M3-PSR), although the M3-PSR was as good as the environmental soil tests if two outliers were omitted. Our results support the development of Mehlich-3 P and M3-PSR categories for profitable agriculture and environmental protection; however, to most accurately characterize the risk of P loss from soil to water by leaching, soil P testing must be fully integrated with other site properties and P management practices.     

Environmental index for estimating the risk of phosphorus loss in calcareous soils of Manitoba

The degree of phosphorus saturation (DPS) has been used in evaluating the risk of P loss from soil to runoff. While techniques are available for calculating DPS for acid soils, no widely used technique exists for neutral to calcareous soils that are typical of the Northern Great Plains, including Manitoba (Canada) soils. This study aimed to develop techniques of calculating the DPS of neutral to alkaline soils. Four measures of soil labile P and ten indices of P sorption capacity were used to calculate the DPS of 115 Manitoba soils. The various DPS calculated were evaluated using water-extractable ((H2O)) P as an index of P susceptibility to runoff loss. The DPS obtained using Olsen-extractable ((Ols)) P and the Langmuir adsorption maximum (ES(max)) ranged from 0.5 to 31.9% while those obtained from P(Ols) and the single-point adsorption index (P(150)) ranged from 0.9 to 73.9%. Of all the DPS evaluated, those that included P(Ols) and Mehlich 3-extractable ((M3)) P as the numerator with either P(150) or ES(max) as the denominator were fairly well correlated with P(H2O) (r values ranged between 0.45 and 0.63). Along with ES(max) and P(150), a new method of calculating DPS was formulated as the ratio of P(Ols) or P(M3) to Ca(M3) or (Ca + Mg)(M3). We found that the ratio of ammonium oxalate-extractable ((ox)) P to (Al + Fe)(ox), which has been widely used to calculate DPS in acid soils, was not suitable for neutral to alkaline soils of Manitoba. In these neutral to alkaline soils, Ca(M3) or (Ca + Mg)(M3) were better indices of P sorption capacity while P(Ols) and P(M3) provided better estimates of labile soil P. The DPS calculated using Ca(M3) or (Ca + Mg)(M3) were well correlated with P(H2O); however, they were numerically smaller than those obtained from the Langmuir adsorption maximum. As such, a saturation coefficient (alpha) with a value of 0.2 was generated to improve the numerical values of the newly estimated DPS. This new approach can be used to estimate the DPS in neutral and calcareous soils without the need to generate a P adsorption maximum.     

Hydrophobicity of soil colloids and heavy metal mobilization: effects of drying

Drying of soil may increase the hydrophobicity of soil and affect the mobilization of colloids after re-wetting. Results of previous research suggest that colloid hydrophobicity is an important parameter in controlling the retention of colloids and colloid-associated substances in soils. We tested the hypothesis that air-drying of soil samples increases the hydrophobicity of water-dispersible colloids and whether air-drying affects the mobilization of colloid-associated heavy metals. We performed batch experiments with field-moist and air-dried (25 degrees C) soils from a former sewage farm (sandy loam), a municipal park (loamy sand), and a shooting range site (loamy sand with 25% C(org)). The filtered suspensions (<1.2 microm) were analyzed for concentrations of dissolved and colloidal organic C and heavy metals (Cu, Cd, Pb, Zn), average colloid size, zeta potential, and turbidity. The hydrophobicity of colloids was determined by their partitioning between a hydrophobic solid and a hydrophilic aqueous phase. Drying increased hydrophobicity of the solid phase but did not affect the hydrophobicity of the dispersed colloids. Drying decreased the amount of mobilized mineral and (organo-)mineral colloids in the sewage farm soils but increased the mobilization of organic colloids in the C-rich shooting range soil. Dried samples released less colloid-bound Cd and Zn than field-moist samples. Drying-induced mobilization of dissolved organic C caused a redistribution of Cu from the colloidal to the dissolved phase. We conclude that drying-induced colloid mobilization is not caused by a change in the physicochemical properties of the colloids. Therefore, it is likely that the mobilization of colloids in the field is caused by increasing shear forces or the disintegration of aggregates.     

Evaluating colloidal phosphorus delivery to surface waters from diffuse agricultural sources

Colloid-facilitated phosphorus (P) delivery from agricultural soils in different hydrological pathways was investigated using a series of laboratory and field experiments. A soil colloidal P test was developed that yields information on the propensity of different soils to release P attached to soil colloids. The relationship between turbidity of soil extracts and total phosphorus (TP) was significant (r2 = 0.996, p < 0.001) across a range of agricultural soils, and a strong positive relationship (r2 = 0.86, p < 0.001) was found between "colloidal P" (H2O-CaCl2 extracts) and turbidity. Linear regression of the proportion of fine clay (<2 microm) for each soil type evaluated against the (H2O-CaCl2) colloidal P fraction gave a weak but positive relationship (r2 = 0.38, p = 0.082). The relative contribution of different particle-size fractions in transporting P in agricultural runoff from grassland soils was evaluated using a randomized plot experiment. A significant difference (p = 0.05) in both TP and reactive phosphorus (RP) in subsurface flow was recorded for different particle-size fractions, with most TP transferred either in association with the 2-microm fraction or with the 0.001-microm or smaller fractions. Total P concentrations in runoff were higher from plots receiving P amendments compared with the zero-P plots; however, these differences were only significant for the >0.45-microm particle-size fractions (p = 0.05), and may be evidence of surface applications of organic and inorganic fertilizers being transferred through the soil either as intact organic colloids or attached to mineral particles. Our results highlight the potential for drainage water to mobilize colloids and associated P during rainfall events.     

Agri-environmental thresholds using Mehlich III soil phosphorus saturation index for vegetables in histosols

The P concentration in Norton Creek which drains cultivated Histosols in Quebec showed median concentration exceeding up to 14 times the environmental guideline of 0.03 mg total P L(-1). The aim of this study was to develop environmental and agronomic thresholds using soil tests to provide a tool for P management in Histosols. Soil samples were collected from Histosols across Quebec (82) and in fertilizer trials (66) to calibrate soil test methods against the degree of P saturation (DPS(OX)) using the acid-oxalate method and setting alpha(m) = 0.4, and the water-extractable P (P(W)) (Sissingh, 1971). The field trials on crop response to added P were conducted with carrots (8), potatoes (11), onions (10), Chinese cabbage (7), celery (10), and lettuce (20). Relative yields were computed as yield in control without P divided by highest yield with added P. The Mehlich III (M-III) P extraction was more closely related (r(2) = 0.73) to DPS(OX) than the Bray 1 method (r(2) = 0.62) and the Florida extraction method (r(2) = 0.53). The [P/(Al+gammaFe)](M-III) ratio as index of P saturation (IPS(M-III)) was the most closely related to DPS(OX) (r(2) = 0.88) setting gamma = 5. The critical [P/(Al+5Fe)](M-III) ratio of 0.05 at DPS(OX) = 0.25 and P(W) = 9.7 mg P L(-1) was validated by an independent study from North Carolina. The soil group (low- vs. high-IPS(M-III) soils) significantly influenced crop response to added P. Critical agronomic IPS(M-III) values were found between 0.10 and 0.15. Those environmental and agronomic benchmarks are instrumental for managing the P in vegetable-grown Histosols.     

Vertical distribution of phosphorus in agricultural drainage ditch soils

Pedological processes such as gleization and organic matter accumulation may affect the vertical distribution of P within agricultural drainage ditch soils. The objective of this study was to assess the vertical distribution of P as a function of horizonation in ditch soils at the University of Maryland Eastern Shore Research Farm in Princess Anne, Maryland. Twenty-one profiles were sampled from 10 agricultural ditches ranging in length from 225 to 550 m. Horizon samples were analyzed for total P; water-extractable P; Mehlich-3 P; acid ammonium oxalate-extractable P, Fe, and Al (P ox, Fe ox, Al ox); pH; and organic C (n = 126). Total P ranged from 27 to 4882 mg kg(-1), P ox from 4 to 4631 mg kg(-1), Mehlich-3 P from 2 to 401 mg kg(-1), and water-extractable P from 0 to 17 mg kg(-1). Soil-forming processes that result in differences between horizons had a strong relationship with various P fractions and P sorption capacity. Fibric organic horizons at the ditch soil surface had the greatest mean P ox, Fe ox, and Al ox concentrations of any horizon class. Gleyed A horizons had a mean Fe ox concentrations 2.6 times lower than dark A horizons and were significantly lower in total P and P ox. Variation in P due to organic matter accumulation and gleization provide critical insight into short- and long-term dynamics of P in ditch soils and should be accounted for when applying ditch management practices.     

Estimating soil phosphorus requirements and limits from oxalate extract data

Excessive fertilizer and manure phosphorus (P) inputs to soils elevates P in soil solution and surface runoff, which can lead to freshwater eutrophication. Runoff P can be related to soil test P and P sorption saturation, but these approaches are restricted to a limited range of soil types or are difficult to determine on a routine basis. The purpose of this study was to determine whether easily measurable soil characteristics were related to the soil phosphorus requirements (P(req), the amount of P sorbed at a particular solution P level). The P(req) was determined for 18 chemically diverse soils from sorption isotherm data (corrected for native sorbed P) and was found to be highly correlated to the sum of oxalate-extractable Al and Fe (R2 > 0.90). Native sorbed P, also determined from oxalate extraction, was subtracted from the P(req) to determine soil phosphorus limits (PL, the amount of P that can be added to soil to reach P(req)). Using this approach, the PL to reach 0.2 mg P L(-1) in solution ranged between -92 and 253 mg P kg(-1). Negative values identified soils with surplus P, while positive values showed soils with P deficiency. The results showed that P, Al, and Fe in oxalate extracts of soils held promise for determining PL to reach up to 10 mg P L(-1) in solution (leading to potential runoff from many soils). The soil oxalate extraction test could be integrated into existing best management practices for improving soil fertility and protecting water quality.     

Colloidal phosphorus in surface runoff and water extracts from semiarid soils of the western United States

Colloidal particles in runoff may have an important role in P transfer from soils to waterbodies, but remain poorly understood. We investigated colloidal molybdate-reactive phosphorus (MRP) in surface runoff and water extracts of calcareous arable soils from the semiarid western United States. Colloidal MRP was determined by ultrafiltration and operationally defined as MRP associated with particles between 1 microm and 1 nm diameter, although a smaller pore-size filter (0.3 nm) was used to define the lower size limit of colloids in water extracts. In surface runoff from three calcareous soils generated by simulated sprinkler irrigation, colloidal MRP concentrations ranged between 0.16 and 3.07 microM, constituting between 11 and 56% of the MRP in the <1-microm fraction. Concentrations were strongly correlated with agronomic and environmental soil-test P concentrations for individual soils. Water extracts of a range of similar soils contained two size fractions of colloidal MRP: a larger fraction (1.0-0.2 microm) probably associated with fine clays, and a smaller fraction (3-0.3 nm) probably associated with Ca-phosphate minerals. Colloidal MRP was solubilized in the acidic medium of the colorimetric detection procedure, suggesting that a fraction of the filterable MRP in runoff from calcareous soils may not be as readily bioavailable as free phosphate in waterbodies. Our results suggest that colloidal MRP is an important but poorly understood component of P transfer in runoff from calcareous western U.S. soils and should be given greater consideration in mechanistic studies of the P transfer process.     

Soil variables for predicting potential phosphorus release in Swedish noncalcareous soils

The accumulation of P in agricultural soils due to fertilization has increased the risk of P losses from agricultural fields to surface waters. In risk assessment systems for P losses, both P release from soil to solution and transport mechanisms need to be considered. In this study, the overall objective was to identify soil variables for prediction of potential P release from soil to solution. Soils from nine sites of the Swedish long-term fertility experiment were used, each with four soil P levels. Phosphorus extractable with CaCl2 was used as an estimate of potential P release from soil to solution. Ammonium lactate-extractable phosphorus (P-AL) or NaHCO3-extractable phosphorus (Olsen P) could not be used alone for prediction of potential P release since soils with high phosphorus sorption capacity (PSC) released less P than soils with low PSC at the same soil test phosphorus (STP) level. Degree of phosphorus saturation (DPS) was calculated as Olsen P or P-AL as a percentage of PSC derived from P sorption isotherms or from Fe and Al extractable in ammonium oxalate. The CaCl2-extractable total phosphorus (CaCl2-TP) was exponentially related to these DPS values (r2 > or = 0.79). The CaCl2-TP was also linearly related to ratios between Olsen P or P-AL and a single-point phosphorus sorption index (PSI; r2 > or = 0.86). These ratios, which are easily determined and gave good correlations with CaCl2-TP, seemed to be the most useful estimates of potential P release for risk assessment systems.     

Phytase supplementation and reduced-phosphorus turkey diets reduce phosphorus loss in runoff following litter application

Concerns about regional surpluses of manure phosphorus (P) leading to increased P losses in runoff have led to interest in diet modification to reduce P concentrations in diets. The objectives of this study were to investigate how dietary P amendment affected P concentrations in litters and P losses in runoff following land application. We grew two flocks of turkeys on the same bed of litter using diets with two levels of non-phytate phosphorus (NPP), with and without phytase. The litters were incorporated into three soils in runoff boxes at a plant-available nitrogen (PAN) rate of 168 kg PAN/ha, with runoff generated on Days 1 and 7 under simulated rainfall and analyzed for dissolved reactive phosphorus (DRP) and total P. Litters were analyzed for water-soluble phosphorus (WSP) and total P, while soils in the runoff boxes were analyzed for WSP and Mehlich-3 phosphorus (M3-P). Formulating diets with lower NPP and phytase both decreased litter total P. Phytase had no significant effect on litter WSP at a 1:200 litter to water extraction ratio, but decreased WSP at a 1:10 extraction ratio. Using a combination of reducing NPP fed and phytase decreased the total P application rate by up to 38% and the P in surplus of crop removal by approximately 48%. Reducing the NPP fed reduced DRP in runoff from litter-amended soils at Day 1, while phytase had no effect on DRP concentrations. Increase in soil M3-P was dependent on total P applied, irrespective of diet. Reducing overfeeding of NPP and utilizing phytase in diets for turkeys should decrease the buildup of P in soils in areas of intensive poultry production, without increasing short-term concerns about dissolved P losses.     

Phosphate release from seasonally flooded soils: a laboratory microcosm study

Phosphorus derived from agricultural practices has been targeted as a leading cause of water quality degradation in Lake Champlain. Mobilization of P from seasonally flooded agricultural soils is a concern. Using 14 soils from a research farm in New York's Champlain Valley, we characterized the available P status, extractable Fe and Al, P sorption capacities, and soluble phosphate release in flooded laboratory microcosms. Quantities of NH4-acetate available P ranged from 3 to 100 mg kg(-1) and fluoride-extractable P from 10 to 211 mg kg(-1). Flooding soils induced significant release of phosphate to the porewater over a 60- to 90-d period in 13 of the 14 soils studied. Porewater phosphate increases ranged from 2.2 to 27.0 times the initial phosphate concentrations. However, floodwater phosphate increases were much lower, with a maximum of 3.6 times the initial concentration. Average porewater phosphate concentrations over the flooding period ranged from 0.046 to 7.0 mg L(-1) and average floodwater P from 0.032 to 3.70 mg L(-1). Ammonium-acetate P and the degree of phosphorus saturation (DPS) were highly correlated with the average porewater and floodwater phosphate concentration. Average ratio of porewater to floodwater phosphate concentrations ranged from 1.0 to 3.3. Five soils that were lower in fluoride-extractable P had increasing porewater phosphate accompanied by increasing porewater Fe2+ and decreasing floodwater phosphate. Results suggest that P solubility and mobility were a function of both the available P status and redox cycling.