Effects of redox on the phosphorus removal ability of iron-rich phosphorus sorption materials.

Iron-rich phosphorus (P) sorption materials (PSMs) are often used in P removal structures, a best management practice able to sequester dissolved P from surface runoff, subsurface drainage, and wastewater. The use of bottom-upward flow in these structures is of great interest, but it creates an intrinsic complication: the presence of stagnant water between flow events may cause structures to develop anoxic conditions. It is unknown whether the redox sensitivity of iron (Fe), the predominant element in Fe-rich PSMs, will affect P binding under anoxic conditions. Understanding the potential impact of intermittent anoxic conditions on the solubility of previously adsorbed P is imperative for determining the feasibility of the bottom-up flow design. The objective of this research was to investigate the (1) development of anoxic conditions in the presence of Fe-rich PSM and tile drainage, (2) Fe-bound P mobilization and solubility, and (3) changes in P sorption capacity of Fe-rich PSMs after oxic conditions are restored. Three Fe-rich PSMs were tested in batch incubation studies: acid mine drainage residual, Fe-coated alumina, and steel metal shavings. Non-treated and P-treated PSM samples were incubated in biogeochemical reactors for as long as necessary to reach Eh = -200 mV. After incubation, dissolved P concentrations in P-treated samples and non-treated samples were similarly low, indicating stability of P retention of PSMs under anoxic conditions. The P removal ability of non-treated PSMs before and after undergoing incubation was not significantly altered, as determined in flow-through experiments. Potentially harmful trace metals were not detected in the incubated solutions. Our research shows that the development of anoxic conditions does not significantly impact PSMs Fe-bound P dissolution, and the P removal ability of PSMs persists after oxic conditions are reestablished.

Phosphate removal by low-cost industrial byproduct iron shavings: Efficacy and longevity.

Iron shavings (IS) are low-cost industrial byproducts that show great potential in removing phosphorus (P) from contaminated water. This work investigates the effectiveness of IS for P (PO4-P) removal and emphasizes its pretreatment and longevity. A 4-d pretreatment of IS with 2.5 % NaCl resulted in a significant increase in P adsorption capacity, from approximately 1.0 to 2.5 mg/g. In column tests, the P removal efficiency remained above 60 % over 60 d, with a capacity of 4.1 mg P/g. Longevity tests involved seven adsorption-regeneration cycles, with an effective IS regeneration by 1 N NaOH and neutralization by HCl solution (pH=2), and the P adsorption capacity only slightly decreased from 2.14 to 1.75 mg P/g. To significantly improve the IS regeneration operation, we employed induction heating and compared an intermittent 10-s induction heating with an isothermal hot NaOH (85 ℃) treatment in 10-min desorption tests (95.3 % versus 56.6 % regeneration). We further found that IH completely regenerated IS in 5 min with 100 s of IH application, but 30 min were needed for hot NaOH (85 ℃) treatment. SEM/EDX, XRD, and XPS tests were conducted to track the changes in the morphology, crystallinity, and surface oxidation products of IS in the cycle tests. Notably, IS surface changed from coarse to smooth with fewer reactive sites and a higher conversion of amorphous Fe oxides to more crystalline Fe3O4, resulting in lower reactivity and fewer exposed Fe0 sites over multiple cycles. All of these mechanisms contributed to the deterioration in P removal capacity. Overall, this study provides a solid foundation for applying low-cost IS in effectively removing P from agricultural runoff.

Techno-Economic Analysis of Phosphorus Removal Structures.

Excess phosphorus (P) is a major pollutant in aquatic systems. Phosphorus removal structures, landscape-scale filters designed to capture dissolved P from runoff, drainage, and wastewater offer promise in curbing P pollution. While the environmental benefits of various P removal structures are well documented, the cost-effectiveness of each structure's ability to sequester P is lacking. In this study, we compare the cost-effectiveness of P removal of the most prominent P removal structures. Specifically, we calculate the average cost per kilogram (kg) of P removed by eight different P removal structures across a range of parameter assumptions. Absent constraints, we found that (1) larger structures that use (2) regionally available phosphorus sorption materials that are (3) byproducts of industrial production (e.g., metal shavings and steel slag) rather than manufactured are more cost-effective. The average cost of P removal for most structures varies from $100 to 1300 per kg in our baseline estimations, which is comparable to the average cost for wastewater treatment. This work provides further information to guide the optimal implementation of P removal structures for conservationists.

Consequences of 33 Years of Plastic Film Mulching and Nitrogen Fertilization on Maize Growth and Soil Quality.

Plastic film mulching and urea nitrogen fertilization are widely used in agricultural ecosystems, but both their long-term use may leave a negative legacy on crop growth, due to deleterious effects of plastic and microplastic accumulation and acidification in soil, respectively. Here, we stopped covering soil with a plastic film in an experimental site that was previously covered for 33 years and compared soil properties and subsequent maize growth and yield between plots that were previously and never covered with the plastic film. Soil moisture was about 5-16% higher at the previously mulched plot than at the never-mulched plot, but NO3- content was lower for the former when with fertilization. Maize growth and yield were generally similar between previously and never-mulched plots. Maize had an earlier dough stage (6-10 days) in previously mulched compared to never-mulched plots. Although plastic film mulching did add substantial amounts of film residues and microplastic accumulation into soils, it did not leave a net negative legacy (given the positive effects of the mulching practice in the first place) for soil quality and subsequent maize growth and yield, at least as an initial effect in our experiment. Long-term urea fertilization resulted in a pH decrease of about 1 unit, which bring a temporary maize P deficiency occurring in early stages of growth. Our data add long-term information on this important form of plastic pollution in agricultural systems.

Estimating the variability of steel slag properties and their influence in phosphorus removal ability.

Steel slag has been proven to be an effective phosphorus (P) removal media, and a potential aid to mitigate point and nonpoint P pollution in freshwater systems. However, the behavior of steel slag as a P sorption material (PSM) is often oversimplified through the generalization of its chemical and physical properties, preventing proper design of P removal structures. In this work, we tested eighteen steel slag samples from different batches, production processes, and steel-making plants, for the purpose of relating slag origin and chemical and physical properties to P removal ability, under two different flow regimes. Slag samples were also coated with aluminum (Al) and tested for P removal. Characterization included elemental composition, particle density, buffer capacity, and P removal ability. There was great variability in the evaluated properties across slag sources and origin, compelling the individual characterization of steel slag samples, since their intrinsic characteristics were key variables in determining their potential P removal capacity. Specifically, electrical conductivity (EC), bulk density, particle density and magnesium (Mg) content could explain around 70% of the variability of P removal by uncoated steel slags. Increasing residence time (RT) always increased P removal for uncoated slags. Steel slags showed a high variability in their P removal ability, but such variability was considerably decreased by coating the slags with Al. Additionally, the Al-coating process significantly improved P removal performance under more rapid flows (lower RT).

Less Agricultural Phosphorus Applied in 2019 Led to Less Dissolved Phosphorus Transported to Lake Erie.

Extreme precipitation events affect water quantity and quality in various regions of the world. Heavy precipitation in 2019 resulted in a record high area of unplanted agricultural fields in the U.S. and especially in the Maumee River Watershed (MRW). March-July phosphorus (P) loads from the MRW drive harmful algal bloom (HAB) severity in Lake Erie; hence changes in management that influence P export can ultimately affect HAB severity. In this study, we found that the 2019 dissolved reactive P (DRP) load from March-July was 29% lower than predicted, while the particulate P (PP) load was similar to the predicted value. Furthermore, the reduced DRP load resulted in a less severe HAB than predicted based on discharge volume. The 29% reduction in DRP loss in the MRW occurred with a 62% reduction in applied P, emphasizing the strong influence of recently applied P and subsequent incidental P losses on watershed P loading. Other possible contributing factors to this reduced load include lower precipitation intensity, altered tillage practices, and effects of fallow soils, but more data is needed to assess their importance. We recommend conservation practices focusing on P application techniques and timing and improving resiliency against extreme precipitation events.

Mechanisms of Phosphorus Removal by Phosphorus Sorbing Materials.

Stormwater filters are a structural best management practice designed to reduce dissolved P losses from runoff. Various industrial byproducts are suitable for use as P sorbing materials (PSMs) for the treatment of drainage water; P sorption by PSMs varies with material physical and chemical properties. Previously, P removal capacity by PSMs was estimated using chemical extractions. We determined the speciation of P when reacted with various PSMs using X-ray absorption near edge structure (XANES) spectroscopy. Twelve PSMs were reacted with P solution in the laboratory under batch or flow-through conditions. In addition, three slag materials were collected from working stormwater filtration structures. Phosphorus K-edge XANES spectra were collected on each reacted PSM and compared with spectra of 22 known P standards using linear combination fitting in Athena. We found evidence of formation of a variety of Ca-, Al-, and/or Fe-phosphate minerals and sorbed phases on the reacted PSMs, with the exact speciation influenced by the chemical properties of the original unreacted PSMs. We grouped PSMs into three general categories based on the dominant P removal mechanism: (i) Fe- and Al-mediated removal [i.e., adsorption of P to Fe- or Al-(hydro-)oxide minerals and/or precipitation of Fe- or Al-phosphate minerals]; (ii) Ca-mediated removal (i.e., precipitation of Ca-phosphate mineral); and (iii) both mechanisms. We recommend the use of Fe/Al sorbing PSMs for use in stormwater filtration structures where stormwater retention time is limited because reaction of P with Fe or Al generally occurs more quickly than Ca-P precipitation.

Investigation of Atrazine Sorption to Biochar With Titration Calorimetry and Flow-Through Analysis: Implications for Design of Pollution-Control Structures.

Atrazine is one of the most common broad-leaf herbicides used in the world. However, due to extensive use for many years, atrazine often appears in surface and groundwater. Atrazine transport is inhibited by degradation or sorption to soil components, especially organic matter. Biochar is a charcoal-like material produced from pyrolysis of biomass. Due to the amount and type of functional groups found on biochar, this product has shown potential for sorption of atrazine from solution. There is an interest in developing best management practices utilizing biochar to filter atrazine from non-point drainage with pollution-control structures such as blind inlets. The objective of this study was to explore the kinetics and thermodynamics of atrazine sorption to biochar using two different approaches: flow-through sorption cells and isothermal titration calorimetry (ITC). Twenty-five milligrams of an oak (Quercus spp.)-derived biochar was suspended in water and titrated 25 times (0.01 mL per titration) with atrazine at three different concentrations, and by a single titration (0.25 mL), with heat of reaction directly measured with ITC. A benchtop atrazine sorption study that simulated the titration experiment was also conducted. A continuous flow-through system was used to quantify the impact of contact time on atrazine sorption to biochar. Atrazine sorption to biochar displayed both exothermic and endothermic signals within each titration, although the net reaction was exothermic and proportional to the degree of sorption. Net enthalpy was -4,231 ± 130 kJ mole-1 atrazine sorbed. The existence of both exotherms and endotherms within a single titration, plus observation of an initial fast reaction phase from 0 to 300 s followed by a slower phase, suggested multiple sorption mechanisms to biochar. Results of flow-through tests supported kinetics observations, with the 300 s contact time removing much more atrazine compared to 45 s, while 600 s improved little compared to 300 s. Based on flow-through results, annual atrazine removal goal of 50%, and typical Midwestern U.S. tile drainage conditions, a pollution-control structure implementing this biochar sample would require 32 and 4 Mg for a design utilizing a contact time of 45 and 300 s, respectively. Future work is necessary for estimating degradation of atrazine sorbed to biochar.

Streambanks: A net source of sediment and phosphorus to streams and rivers.

Sediment and phosphorus (P) are two primary pollutants of surface waters. Many studies have investigated loadings from upland sources or even streambed sediment, but in many cases, limited to no data exist to determine sediment and P loading from streambanks on a watershed scale. The objectives of this paper are to review the current knowledge base on streambank erosion and failure mechanisms, streambank P concentrations, and streambanks as P loading sources and then also to identify future research needs on this topic. In many watersheds, long-term loading of soil and associated P to stream systems has created a source of eroded soil and P that may interact with streambank sediment and be deposited in floodplains downstream. In many cases streambanks were formed from previously eroded and deposited alluvial material and so the resulting soils possess unique physical and chemical properties from adjacent upland soils. Streambank sediment and P loading rates depend explicitly on the rate of streambank migration and the concentration of P stored within bank materials. From the survey of literature, previous studies report streambank total P concentrations that consistently exceeded 250 mg kg(-1) soil. Only a few studies also reported water soluble or extractable P concentrations. More research should be devoted to understanding the dynamic processes between different P pools (total P versus bioavailable P), and sorption or desorption processes under varying hydraulic and stream chemistry conditions. Furthermore, the literature reported that streambank erosion and failure and gully erosion were reported to account for 7-92% of the suspended sediment load within a channel and 6-93% of total P. However, significant uncertainty can occur in such estimates due to reach-scale variability in streambank migration rates and future estimates should consider the use of uncertainty analysis approaches. Research is also needed on the transport rates of dissolved and sediment-bound P through the entire stream system of a watershed to identify critical upland and/or near-stream conservation practices. Extensive monitoring of the impact of restoration/rehabilitation efforts on reducing sediment and P loading are limited. From an application standpoint, streambank P contributions to streams should be more explicitly accounted for in developing total maximum daily loads in watersheds.

Phosphate sorption by three potential filter materials as assessed by isothermal titration calorimetry.

Phosphorus eutrophication of lakes and streams, coming from drained farmlands, is a serious problem in areas with intensive agriculture. Installation of phosphate (P) sorbing filters at drain outlets may be a solution. The aim of this study was to improve the understanding of reactions involved in P sorption by three commercial P sorbing materials, i.e. Ca/Mg oxide-based Filtralite-P, Fe oxide-based CFH-12 and Limestone in two particle sizes (2-1 mm and 1-0.5 mm), by means of isothermal titration calorimetry (ITC), sorption isotherms, sequential extractions and SEM-EDS. The results indicate that P retention by CFH is due to surface complexation by rapid formation of strong Fe-P bonds. In contrast, retention of P by Filtralite-P and Limestone strongly depends on pH and time and is interpreted due to formation of calcium phosphate precipitate(s). Consequently, CFH can unambiguously be recommended as P retention filter material in drain outlets, whereas the use of Filtralite-P and Limestone has certain (serious) limitations. Thus, Filtralite-P has high capacity to retain P but only at alkaline pH (pH ≥ 10) and P retention by Limestone requires long-time contact and a high ratio between sorbent and sorbate.

Forage and tree seedling growth in a soil with an encased swine sludge layer.

The closure of swine farms requires decommissioning of lagoons that contain large amounts of swine solids (sludge). Sludge is typically transported and land applied to soils. However, in some cases this process could be economically prohibitive and/or unpractical. An alternative idea is to encase sludge with lagoon soil berms after removing overlying effluent, followed by establishment of forages or short-rotation woody crops on the encased sludge. The objective of this study was to investigate growth potential for several forages and tree species into a pure layer of swine sludge. Alfalfa (Meticago sativa), bermudagrass (Cynodon dactylon), switchgrass (Panicum virgatum), green ash (Fraxinus pennsylvanica), black locust (Robinia pseudoacacia), and sycamore (Platanus occidentalis) were established in 40 cm deep pots consisting of a lagoon berm soil overlaying a sludge layer for 12 w followed by analysis of aboveground and belowground biomass production. "New" and "old" sludge was collected from an active 10 year old lagoon and decommissioned 50 year old lagoon, respectively. A control (soil only) was used. Encased sludge treatments increased forage biomass production. Sycamore and green ash were sensitive to new sludge but not old sludge as these species had less biomass production in new sludge than control and showed tissue trace nutrient deficiencies. While both sludge materials contained adequate nutrients, the new sludge had a salt concentration 1.8 times higher than old sludge as indicated by electrical conductivity (12.4 mS). Thus, the forage crops and black locust were able to thrive in new sludge due to their salt tolerance.

Trapping phosphorus in runoff with a phosphorus removal structure.

Reduction of phosphorus (P) inputs to surface waters may decrease eutrophication. Some researchers have proposed filtering dissolved P in runoff with P-sorptive byproducts in structures placed in hydrologically active areas with high soil P concentrations. The objectives of this study were to construct and monitor a P removal structure in a suburban watershed and test the ability of empirically developed flow-through equations to predict structure performance. Steel slag was used as the P sorption material in the P removal structure. Water samples were collected before and after the structure using automatic samples and analyzed for total dissolved P. During the first 5 mo of structure operation, 25% of all dissolved P was removed from rainfall and irrigation events. Phosphorus was removed more efficiently during low flow rate irrigation events with a high retention time than during high flow rate rainfall events with a low retention time. The six largest flow events occurred during storm flow and accounted for 75% of the P entering the structure and 54% of the P removed by the structure. Flow-through equations developed for predicting structure performance produced reasonable estimates of structure "lifetime" (16.8 mo). However, the equations overpredicted cumulative P removal. This was likely due to differences in pH, total Ca and Fe, and alkalinity between the slag used in the structure and the slag used for model development. This suggests the need for an overall model that can predict structure performance based on individual material properties.

Alternative poultry litter storage for improved transportation and use as a soil amendment.

Transportation of poultry litter out of nutrient limited watersheds such as the Illinois River basin (eastern Oklahoma) is a logical solution for minimizing phosphorus (P) losses from soils to surface waters. Transportation costs are basedon mass of load and distance transported. This study investigated an alternative litter storage technique designed to promote carbon (C) degradation, thereby concentrating nutrients for the purpose of decreasing transportation costs through decreased mass. Poultry litter was stored in 0.90-Mg conical piles under semipermeable tarps and adjusted to 40% moisture content, tested with and without addition of alum (aluminum sulfate). additional study was conducted using 3.6-Mg piles under the same conditions, except tested with and without use of aeration pipes. Samples were analyzed before and after (8 wk) storage. Litter mass degradation (i.e., loss in mass due to organic matter decomposition) was estimated on the basis of changes in litter total P contents. Additional characterization included pH, total nutrients, moisture content, total C, and degree of humification. Litter storage significantly decreased litter mass (16 to 27%), concentrated nutrients such as P and potassium (K) and increased proportion of fulvic and humic acids. The addition of aeration pipes increased mass degradationrelative to piles without aeration pipes. Nitrogen volatilization losses were minimized with alum additions. Increases in P and K concentrations resulted in greater monetary value per unit mass compared with fresh litter. Such increases translate to increased litter shipping distance and cost savings of $17.2 million over 25 yr for litter movement out of eastern Oklahoma.

Maximizing ammonium nitrogen removal from solution using different zeolites.

Zeolite minerals are ideal for removing ammonium nitrogen (NH4(+)-N) from animal wastes, leachates, and industrial effluents. The objectives of this study were to compare NH4+ removal and kinetics among several commercially available zeolites under various conditions and determine if calorimetry could provide information regarding kinetics of NH4+ removal. Ammonium sorption onto potassium (K) saturated zeolites was compared using synthetic vs. natural swine effluent and with either traditional batch-shaken system or a "tea bag" approach in which zeolites were contained in a mesh sack and suspended in a solution of swine effluent. Ammonium sorption was measured at four retention times using a flow-through system, and the resulting heat response was measured using isothermal calorimetry. Ammonium removal was not significantly different in synthetic vs. natural swine effluent. Ammonium removal was lower in batch-stirred compared to batch-shaken systems, suggesting that diffusion between particles was rate-limiting in the former system. Flow-through cells possessing contact times > 100 s displayed greater NH4+ sorption than batch systems, suggesting that maintaining high NH4+ concentration in solution, removal of exchange products, and sufficient reaction time are critical to maximizing NH4+ removal by zeolites. Within 100 s after NH4+ addition, endothermic heat responses indicated that NH4(+)-K+ exchange had peaked; this was followed by significant heat rate reduction for 50 min. This confirmed findings of an initial fast NH4(+)-K+ exchange followed by a slower one and suggests the 100-s period of rapid reaction is an indicator of the minimum flow through retention time required to optimize NH4+ sorption to zeolites used in this study.

Subsurface transport of phosphorus in riparian floodplains: influence of preferential flow paths.

For phosphorus (P) transport from upland areas to surface water systems, the primary transport mechanism is typically considered to be surface runoff with subsurface transport assumed negligible. However, certain local conditions can lead to an environment where subsurface transport may be significant. The objective of this research was to determine the potential of subsurface transport of P along streams characterized by cherty or gravel subsoils, especially the impact of preferential flow paths on P transport. At a field site along the Barren Fork Creek in northeastern Oklahoma, a trench was installed with the bottom at the topsoil/alluvial gravel interface. Fifteen piezometers were installed surrounding the trench to monitor flow and transport. In three experiments, water was pumped into the trench from the Barren Fork Creek to maintain a constant head. At the same time, a conservative tracer (Rhodamine WT) and/or potassium phosphate solution were injected into the trench at concentrations at 3 and 100 mg/L for Rhodamine WT and at 100 mg/L for P. Laboratory flow-cell experiments were also conducted on soil material <2 mm in size to determine the effect that flow velocity had on P sorption. Rhodamine WT and P were detected in some piezometers at equivalent concentrations as measured in the trench, suggesting the presence of preferential flow pathways and heterogeneous interaction between streams and subsurface transport pathways, even in nonstructured, coarse gravel soils. Phosphorus transport was retarded in nonpreferential flow paths. Breakthrough times were approximately equivalent for Rhodamine WT and P suggesting no colloidal-facilitated P transport. Results from laboratory flow-cell experiments suggested that higher velocity resulted in less P sorption for the alluvial subsoil. Therefore, differences in flow rates between preferential and nonpreferential flow pathways in the field led to variable sorption. The potential for nutrient subsurface transport shown by this alluvial system has implications regarding management of similar riparian floodplain systems.

The impact of alum addition on organic P transformations in poultry litter and litter-amended soil.

Poultry litter treatment with alum (Al(2)(SO(4))(3) . 18H(2)O) lowers litter phosphorus (P) solubility and therefore can lower litter P release to runoff after land application. Lower P solubility in litter is generally attributed to aluminum-phosphate complex formation. However, recent studies suggest that alum additions to poultry litter may influence organic P mineralization. Therefore, alum-treated and untreated litters were incubated for 93 d to assess organic P transformations during simulated storage. A 62-d soil incubation was also conducted to determine the fate of incorporated litter organic P, which included alum-treated litter, untreated litter, KH(2)PO(4) applied at 60 mg P kg(-1) of soil, and an unamended control. Liquid-state (31)P nuclear magnetic resonance indicated that phytic acid was the only organic P compound present, accounting for 50 and 45% of the total P in untreated and alum-treated litters, respectively, before incubation and declined to 9 and 37% after 93 d of storage-simulating incubation. Sequential fractionation of litters showed that alum addition to litter transformed 30% of the organic P from the 1.0 mol L(-1) HCl to the 0.1 mol L(-1) NaOH extractable fraction and that both organic P fractions were more persistent in alum-treated litter compared with untreated litter. The soil incubation revealed that 0.1 mol L(-1) NaOH-extractable organic P was more recalcitrant after mixing than was the 1.0 mol L(-1) HCl-extractable organic P. Thus, adding alum to litter inhibits organic P mineralization during storage and promotes the formation of alkaline extractable organic P that sustains lower P solubility in the soil environment.

Environmental and production consequences of using alum-amended poultry litter as a nutrient source for corn.

Field trials were established to compare alum-treated poultry litter (ATPL), normal poultry litter (NPL), and triple superphosphate (TSP) as fertilizer sources for corn (Zea mays L.) when applied at rates based on current litter management strategies in Virginia. Trials were established in the Costal Plain and Piedmont physiographic regions near Painter and Orange, VA, respectively. Nitrogen-based applications of ATPL or NPL applied at rates estimated to supply 173 kg of plant-available nitrogen (PAN) ha(-1) resulted in significantly lower grain yields than treatments receiving commercial fertilizer at the same rate in 2000 and 2001 at Painter. These decreases in grain yield at the N-based application rates were attributed to inadequate N availability, resulting from overestimates of PAN as demonstrated by tissue N concentrations. However, at Orange no treatment effects on grain yield were observed. Applications of ATPL did not affect Al concentrations in corn ear-leaves at either location. Exchangeable soil Al concentrations were most elevated in treatments receiving only NH4NO3 as an N source. At N-based application rates, the ATPL resulted in lower Mehlich 1-extractable P (M1-P) and water-extractable soil phosphorus (H2O-P) concentrations compared to the application of NPL. A portion of this reduction could be attributed to lower rates of P applied in the N-based ATPL treatments. Runoff collected from treatments which received ATPL 2 d before conducting rainfall simulations contained 61 to 71% less dissolved reactive phosphorus (DRP) than treatments receiving NPL. These results show that ATPL may be used as a nutrient source for corn production without significant management alterations. Alum-treated poultry litter can also reduce the environmental impact of litter applications, primarily through minimizing the P status of soils receiving long-term applications of litter and reductions in runoff DRP losses shortly after application.

Phosphorus forms in biosolids-amended soils and losses in runoff: effects of wastewater treatment process.

Continuous addition of municipal biosolids to soils based on plant nitrogen (N) requirements can cause buildup of soil phosphorus (P) in excess of crop requirements; runoff from these soils can potentially contribute to nonpoint P pollution of surface waters. However, because biosolids are often produced using lime and/or metal salts, the potential for biosolids P to cause runoff P losses can vary with wastewater treatment plant (WWTP) process. This study was conducted to determine the effect of wastewater treatment process on the forms and amounts of P in biosolids, biosolids-amended soils, and in runoff from biosolids-amended soils. We amended two soil types with eight biosolids and a poultry litter (PL) at equal rates of total P (200 kg ha(-1); unamended soils were used as controls. All biosolids and amended soils were analyzed for various types of extractable P, inorganic P fractions, and the degree of P saturation (acid ammonium oxalate method). Amended soils were placed under a simulated rainfall and all runoff was collected and analyzed for dissolved reactive phosphorus (DRP), iron-oxide-coated filter paper strip-extractable phosphorus (FeO-P), and total phosphorus (EPA3050 P). Results showed that biosolids produced with a biological nutrient removal (BNR) process caused the highest increases in extractable soil P and runoff DRP. Alternatively, biosolids produced with iron only consistently had the lowest extractable P and caused the lowest increases in extractable soil P and runoff DRP when added to soils. Differences in soil and biosolids extractable P levels as well as P runoff losses were related to the inorganic P forms of the biosolids.