The effects of soil carbon on phosphorus and sediment loss from soil trays by overland flow

Soil chemical constituents influence soil structure and erosion potential. We investigated manure and inorganic fertilizer applications on soil chemistry (carbon [C] quality and exchangeable cations), aggregation, and phosphorus (P) loss in overland flow. Surface samples (0-5 cm) of a Hagerstown (fine, mixed, semiactive, mesic Typic Hapludalf) soil, to which either dairy or poultry manure or triple superphosphate had been applied (0-200 kg P ha(-1) yr(-1) for 5 yr), were packed in boxes (1 m long, 0.15 m wide, and 0.10 m deep) to field bulk density (1.2 g cm(-3)). Rainfall was applied (65 mm h(-1)), overland flow collected, and sediment and P loss determined. All amendments increased Mehlich 3-extractable P (19-177 mg kg(-1)) and exchangeable Ca (4.2-11.5 cmol kg(-1)) compared with untreated soil. For all treatments, sediment transport was inversely related to the degree of soil aggregation (determined as ratio of dispersed and undispersed clay; r = 0.51), exchangeable Ca (r = 0.59), and hydrolyzable carbohydrate (r = 0.62). The loss of particulate P and total P in overland flow from soil treated with up to 50 kg P ha(-1) dairy manure (9.9 mg particulate phosphorus [PPI, 15.1 mg total phosphorus [TP]) was lower than untreated soil (13.3 mg PP, 18.1 mg TP), due to increased aggregation and decreased surface soil slaking attributed to added C in manure. Manure application at low rates (<50 kg P ha(-1)) imparts physical benefits to surface soil, which decrease P loss potential. However, at greater application rates, P transport is appreciably greater (26.9 mg PP, 29.5 mg TP) than from untreated soil (13.3 mg PP, 18.1 mg TP).     

Interactions between soil texture and placement of dairy slurry application: II. Leaching of phosphorus forms

Managing phosphorus (P) losses in soil leachate folllowing land application of manure is key to curbing eutrophication in many regions. We compared P leaching from columns of variably textured, intact soils (20 cm diam., 20 cm high) subjected to surface application or injection of dairy cattle (Bos taurus L.) manure slurry. Surface application of slurry increased P leaching losses relative to baseline losses, but losses declined with increasing active flow volume. After elution of one pore volume, leaching averaged 0.54 kg P ha(-1) from the loam, 0.38 kg P ha(-1) from the sandy loam, and 0.22 kg P ha(-1) from the loamy sand following surface application. Injection decreased leaching of all P forms compared with surface application by an average of 0.26 kg P ha(-1) in loam and 0.23 kg P ha(-1) in sandy loam, but only by 0.03 kg P ha(-1) in loamy sand. Lower leaching losses were attributed to physical retention of particulate P and dissolved organic P, caused by placing slurry away from active flow paths in the fine-textured soil columns, as well as to chemical retention of dissolved inorganic P, caused by better contact between slurry P and soil adsorption sites. Dissolved organic P was less retained in soil after slurry application than other P forms. On these soils with low to intermediate P status, slurry injection lowered P leaching losses from clay-rich soil, but not from the sandy soils, highlighting the importance of soil texture in manageing P losses following slurry application.     

Land application of domestic effluent onto four soil types: plant uptake and nutrient leaching

Land application has become a widely applied method for treating wastewater. However, it is not always clear which soil-plant systems should be used, or why. The objectives of our study were to determine if four contrasting soils, from which the pasture is regularly cut and removed, varied in their ability to assimilate nutrients from secondary-treated domestic effluent under high hydraulic loadings, in comparison with unirrigated, fertilized pasture. Grassed intact soil cores (500 mm in diameter by 700 mm in depth) were irrigated (50 mm wk(-1)) with secondary-treated domestic effluent for two years. Soils included a well-drained Allophanic Soil (Typic Hapludand), a poorly drained Gley Soil (Typic Endoaquept), a well-drained Pumice Soil formed from rhyolitic tephra (Typic Udivitrand), and a well-drained Recent Soil formed in a sand dune (Typic Udipsamment). Effluent-irrigated soils received between 746 and 815 kg N ha(-1) and 283 and 331 kg P ha(-1) over two years of irrigation, and unirrigated treatments received 200 kg N ha(-1) and 100 kg P ha(-1) of dissolved inorganic fertilizer over the same period. Applying effluent significantly increased plant uptake of N and P from all soil types. For the effluent-irrigated soils plant N uptake ranged from 186 to 437 kg N ha(-1) yr(-1), while plant P uptake ranged from 40 to 88 kg P ha(-1) yr(-1) for the effluent-irrigated soils. Applying effluent significantly increased N leaching losses from Gley and Recent Soils, and after two years ranged from 17 to 184 kg N ha(-1) depending on soil type. Effluent irrigation only increased P leaching from the Gley Soil. All P leaching losses were less than 49 kg P ha(-1) after two years. The N and P leached from effluent treatments were mainly in organic form (69-87% organic N and 35-65% unreactive P). Greater N and P leaching losses from the irrigated Gley Soil were attributed to preferential flow that reduced contact between the effluent and the soil matrix. Increased N leaching from the Recent Soil was the result of increased leaching of native soil organic N due to the higher hydraulic loading from the effluent irrigation.     

Effects of soil phosphorus status on environmental risk assessment of glyphosate and glufosinate-ammonium

The increased use of herbicides poses a risk to the aquatic environment. Easy and economical methods are needed to identify the fields where specific environment protection measures are needed. Phosphorus (P) and organophosphorus herbicides compete for the same adsorption sites in soil. In this study the relationship between P obtained in routine Finnish agronomic tests (acid ammonium acetate [P(AC)]) and adsorption of glyphosate and glufosinate-ammonium was investigated to determine whether P(AC) values could be used in the risk assessment. The adsorption of glyphosate ((N-(phosphonomethyl)glycine) and glufosinate-ammonium (2-amino-4-(hydroxymethylphosphinyl)butanoic acid) was studied in a clay and a sandy loam soil enriched with increasing amounts of P added as potassium dihydrogen phosphate. Desorption was also determined for some P-enriched soil samples. The adsorption of both herbicides diminished with increasing P(AC) value. The correlations between Freundlich adsorption coefficients obtained in the adsorption tests and P(AC) were nonlinear but significant (r > 0.98) in both soils. The exponential models of the relationship between soil P(AC) values and glyphosate adsorption were found to fit well to an independent Finnish soil data set (P < 0.1 for glyphosate and P < 0.01 for glufosinate-ammonium). The desorption results showed that glufosinate-ammonium sorption is not inversely related to soil P status, and the high correlation coefficients obtained in the test of the model were thus artifacts caused by an abnormal concentration of exchangeable potassium in soil. The solved equations are a useful tool in assessing the leaching risks of glyphosate, but their use for glufosinate-ammonium is questionable.     

Chicken manure biochar as liming and nutrient source for acid Appalachian soil

Acid weathered soils often require lime and fertilizer application to overcome nutrient deficiencies and metal toxicity to increase soil productivity. Slow-pyrolysis chicken manure biochars, produced at 350 and 700°C with and without subsequent steam activation, were evaluated in an incubation study as soil amendments for a representative acid and highly weathered soil from Appalachia. Biochars were mixed at 5, 10, 20, and 40 g kg into a Gilpin soil (fine-loamy, mixed, active, mesic Typic Hapludult) and incubated in a climate-controlled chamber for 8 wk, along with a nonamended control and soil amended with agronomic dolomitic lime (AgLime). At the end of the incubation, soil pH, nutrient availability (by Mehlich-3 and ammonium bicarbonate diethylene triamine pentaacetic acid [AB-DTPA] extractions), and soil leachate composition were evaluated. Biochar effect on soil pH was process- and rate-dependent. Biochar increased soil pH from 4.8 to 6.6 at the high application rate (40 g kg), but was less effective than AgLime. Biochar produced at 350°C without activation had the least effect on soil pH. Biochar increased soil Mehlich-3 extractable micro- and macronutrients. On the basis of unit element applied, increase in pyrolysis temperature and biochar activation decreased availability of K, P, and S compared to nonactivated biochar produced at 350°C. Activated biochars reduced AB-DTPA extractable Al and Cd more than AgLime. Biochar did not increase NO in leachate, but increased dissolved organic carbon, total N and P, PO, SO, and K at high application rate (40 g kg). Risks of elevated levels of dissolved P may limit chicken manure biochar application rate. Applied at low rates, these biochars provide added nutritional value with low adverse impact on leachate composition.     

Polyphenols dynamics and phytotoxicity in a soil amended by olive mill wastewaters

The effects of unprocessed olive mill wastewaters (OMW) on soil characteristics were investigated. Phenolic compounds levels in the treated soil were compared to those of a control soil profile. Results showed that OMW infiltration caused a modification of soil physicochemical characteristics. Phenolic compounds were detected at a depth of 1.2m four months after the last application of OMW. A moderate phytotoxic residual phenolic fraction (F) was extracted from the superficial soil layer 1 year after the OMW application. This residual F had a phytotoxic potential comparable to that of 25-fold diluted OMW.     

Amendment effects on soil test phosphorus

Applications of animal manures have increased soil test P values in many parts of the USA and thus increased the risk that soil P will be transferred to surface water and decrease water quality. To continue farming these areas, landowners need tools to reduce the risk of P losses. A field experiment was conducted near Kurten, TX, on a Zulch fine sandy loam (thermic Udertic Paleustalfs) with Bray-1 P values exceeding 3000 mg P kg(-1) soil (dry wt.) in the A(p) horizon to evaluate the effectiveness of soil amendments for reducing soil test P values. Soils were amended annually from 1999 to 2001 with 1.5 and 5.0 Mg gypsum ha(-1), 1.4 Mg alum ha(-1), or 24.4 Mg ha(-1) of waste paper product high in Al alone or in combination with 1.5 Mg gypsum ha(-1) and/or 1.4 Mg alum ha(-1). These treatments supplied a maximum of 225 and 1163 kg ha(-1) yr(-1) of Al and Ca, respectively. Soil Bray-1 P and dissolved reactive P levels were monitored from 1999 to 2004. None of the soil amendment treatments affected Bray-1 P values. Only annual additions of 5.0 Mg gypsum ha(-1) from 1999 to 2001 significantly reduced soil dissolved reactive P. Dissolved reactive P levels reached minimal levels after two applications of 5.0 Mg gypsum ha(-1) but increased in 2003 and 2004. These results indicate that soil dissolved reactive P levels can be reduced if sufficient amounts of gypsum were added to supply Ca in amounts similar to the soil test P values.     

Long-term effect of a single application of organic refuse on carbon sequestration and soil physical properties

Restoration of degraded lands could be a way to reverse soil degradation and desertification in semiarid areas and mitigate greenhouse gases (GHG). Our objective was to evaluate the long-term effects of a single addition of organic refuse on soil physical properties and measure its carbon sequestration potential. In 1988, a set of five plots (87 m(2) each) was established in an open desert-like scrubland (2-4% cover) in Murcia, Spain, to which urban solid refuse (USR) was added in a single treatment at different rates. Soil properties were monitored over a 5-yr period. Sixteen years after the addition, three of the plots were monitored again (P0: control, P1: 13 kg m(-2), P2: 26 kg m(-2) of USR added) to assess the lasting effect of the organic addition on the soil organic carbon (SOC) pools and on the physical characteristics of the soil. The SOC content was higher in P2 (16.4 g kg(-1)) and in P1 (11.8 g kg(-1)) than in P0 (7.9 g kg(-1)). Likewise, aerial biomass increased from 0.18 kg m(-2) in P0 up to 0.27 kg m(-2) in P1 and 0.46 kg m(-2) in P2. This represents a total C sequestration of 9.5 Mg ha(-1) in P2 and 3.4 Mg ha(-1) in P1, most of the sequestered C remaining in the recalcitrant soil pool. Additionally, higher saturated hydraulic conductivity, aggregate stability, and available water content values and lower bulk density values were measured in the restored plots. Clearly, a single addition of organic refuse to the degraded soils to increase the potential for C sequestration was effective.     

Residual soil nitrate after potato harvest

Nitrogen loss by leaching is a major problem, particularly with crops requiring large amounts of N fertilizer. We evaluated the effect of N fertilization and irrigation on residual soil nitrate following potato (Solanum tuberosum L.) harvests in the upper St-John River valley of New Brunswick, Canada. Soil nitrate contents were measured to a 0.90-m depth in three treatments of N fertilization (0, 100, and 250 kg N ha(-1)) at two on-farm sites in 1995, and in four treatments of N fertilization (0, 50, 100, and 250 kg N ha(-1)) at four sites for each of two years (1996 and 1997) with and without supplemental irrigation. Residual soil NO3-N content increased from 33 kg NO3-N ha(-1) in the unfertilized check plots to 160 kg NO3-N ha(-1) when 250 kg N ha(-1) was applied. Across N treatments, residual soil NO3-N contents ranged from 30 to 105 kg NO3-N ha(-1) with irrigation and from 30 to 202 kg NO3-N ha(-1) without irrigation. Residual soil NO3-N content within the surface 0.30 m was related (R2 = 0.94) to the NO3-N content to a 0.90-m depth. Estimates of residual soil NO3-N content at the economically optimum nitrogen fertilizer application (Nop) ranged from 46 to 99 kg NO3-N ha(-1) under irrigated conditions and from 62 to 260 kg NO3-N ha(-1) under nonirrigated conditions, and were lower than the soil NO3-N content measured with 250 kg N ha(-1). We conclude that residual soil NO3-N after harvest can be maintained at a reasonable level (<70 kg NO3-N ha(-1)) when N fertilization is based on the economically optimum N application.     

Impact of intensive market gardening on the nutrient status of hydromorphic soil in the Ojo area of Lagos metropolis,Nigeria

Summary This study evaluates the impact of intensive market gardening on the nutrient status of hydromorphic soil in the Ojo area of Lagos metropolis. Following 15–20 years of continuous market gardening, the organic matter content of the 0–10 cm layer of the hydromorphic soil has been reduced to 75 percent of the level found in a swamp forest soil used as a control. The extent of the organic matter decline in the cultivated soil is slight compared with the degree of organic matter diminution in well-drained soil used for shifting or continuous cultivation. This is due to the low degree of humus mineralisation in water-logged soil and the application of organic manure.In spite of regular application of both organic and inorganic fertilisers, the levels of exchangeable calcium, magnesium, potassium and sodium are lower in the 0–10 cm and 10–20 cm layers of the intensively cultivated hydromorphic soil used for market gardening than in the swamp forest control areas. The mean level of extractable manganese is lower in the 10–20 cm layer of the cultivated soil. These differences are due to nutrient immobilisation and removal in harvested vegetables, and to nutrient loss from the market gardening plots through erosion. There is, however, a build-up of available phosphorus in the surface layer of the market garden soil due to the application of inorganic phosphate fertilisers.The levels of mineral nutrients in the surface layers of the cultivated soil are within the optimal ranges for most arable crops, suggesting that the soil is not impoverished. This is due to the judicious application of both organic and inorganic fertilisers, and is indicative of the fact that hydromorphic soils can support continuous cultivation under proper management.Dr A.O. Aweto is a Senior Lecturer in the Department of Geography, and Mr G.M. Ogurie was until recently a geography student in the same department.     

CONTROLLING PHOSPHORUS IN RUNOFF FROM LONG TERM DAIRY WASTE APPLICATION FIELDS1

ABSTRACT: Phosphorus (P) in runoff from long term animal waste application fields can contribute to accelerated eutrophication of surface waters. Manure when applied at nitrogen (N) agronomic rates generally increases soil P concentrations, which can increase runoff of soluble P. Along the North Bosque River in central Texas, dairy waste application fields are identified as the most controllable nonpoint source of soluble P in a total maximum daily load. To evaluate P reduction practices for fields high in soil extractable P, edge‐of‐field runoff was measured from paired plots of Coastal bermudagrass (Cynodon dactylon) and sorghum (Sorghum bicolor)/ winter wheat (Triticum spp.). Plots (about 0.4 ha) received manure at P agronomic rates following Texas permit guidelines and commercial N during the pretreatment period. During the post‐treatment period, control plots continued to receive manure at P agronomic rates and commercial N. Treatment plots received only commercial N during the post‐treatment period. Use of only commercial N on soils with high extractable P levels significantly decreased P loadings in edge‐of‐field runoff by at least 40 percent, but runoff concentrations sometimes increased. No notable changes in extractable soil P concentrations were observed after five years of monitoring due to drought conditions limiting forage uptake and removal.     

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.     

Runoff phosphorus losses as related to phosphorus source, application method, and application rate on a Piedmont soil

Land application of animal manures and fertilizers has resulted in an increased potential for excessive P losses in runoff to nutrient-sensitive surface waters. The purpose of this research was to measure P losses in runoff from a bare Piedmont soil in the southeastern United States receiving broiler litter or inorganic P fertilizer either incorporated or surface-applied at varying P application rates (inorganic P, 0-110 kg P ha(-1); broiler litter, 0-82 kg P ha(-1)). Rainfall simulation was applied at a rate of 76 mm h(-1). Runoff samples were collected at 5-min intervals for 30 min and analyzed for reactive phosphorus (RP), algal-available phosphorus (AAP), and total phosphorus (TP). Incorporation of both P sources resulted in P losses not significantly different than the unfertilized control at all application rates. Incorporation of broiler litter decreased flow-weighted concentration of RP in runoff by 97% and mass loss of TP in runoff by 88% compared with surface application. Surface application of broiler litter resulted in runoff containing between 2.3 and 21.8 mg RP L(-1) for application rates of 8 to 82 kg P ha(-1), respectively. Mass loss of TP in runoff from surface-applied broiler litter ranged from 1.3 to 8.5 kg P ha(-1) over the same application rates. Flow-weighted concentrations of RP and mass losses of TP in runoff were not related to application rate when inorganic P fertilizer was applied to the soil surface. Results for this study can be used by P loss assessment tools to fine-tune P source, application rate, and application method site factors, and to estimate extreme-case P loss from cropland receiving broiler litter and inorganic P fertilizers.     

Long-term effects of poultry litter, alum-treated litter, and ammonium nitrate on aluminum availability in soils

Research has shown that alum [Al(2)(SO(4))(3).14H(2)O] applications to poultry litter can greatly reduce phosphorus (P) runoff, as well as decrease ammonia (NH(3)) volatilization. However, the long-term effects of fertilizing with alum-treated litter are unknown. The objectives of this study were to evaluate the long-term effects of normal poultry litter, alum-treated litter, and ammonium nitrate (NH(4)NO(3)) on aluminum (Al) availability in soils, Al uptake by tall fescue (Festuca arundinacea Schreb.), and tall fescue yields. A long-term study was initiated in April of 1995. There were 13 treatments (unfertilized control, four rates of normal litter, four rates of alum-treated litter, and four rates of NH(4)NO(3)) in a randomized block design. All fertilizers were broadcast applied to 52 small plots (3.05 x 1.52 m) cropped to tall fescue annually in the spring. Litter application rates were 2.24, 4.49, 6.73, and 8.98 Mg ha(-1) (1, 2, 3, and 4 tons acre(-1)); NH(4)NO(3) rates were 65, 130, 195, and 260 kg N ha(-1) and were based on the amount of N applied with alum-treated litter. Soil pH, exchangeable Al (extracted with potassium chloride), Al uptake by fescue, and fescue yields were monitored periodically over time. Ammonium nitrate applications resulted in reductions in soil pH beginning in Year 3, causing exchangeable Al values to increase from less than 1 mg Al kg(-1) soil in Year 2 to over 100 mg Al kg(-1) soil in Year 7 for many of the NH(4)NO(3) plots. In contrast, normal and alum-treated litter resulted in an increase in soil pH, which decreased exchangeable Al when compared to unfertilized controls. Severe yield reductions were observed with NH(4)NO(3) beginning in Year 6, which were due to high levels of acidity and exchangeable Al. Aluminum uptake by forage and Al runoff from the plots were not affected by treatment. Fescue yields were highest with alum-treated litter (annual average = 7.36 Mg ha(-1)), followed by normal litter (6.93 Mg ha(-1)), NH(4)NO(3) (6.16 Mg ha(-1)), and the control (2.89 Mg ha(-1)). These data indicate that poultry litter, particularly alum-treated litter, may be a more sustainable fertilizer than NH(4)NO(3).     

Long-term phosphorus fertility in wastewater-irrigated cropland

Land treatment of municipal wastewater effluent is a proven method for augmenting freshwater resources and avoiding direct nutrient discharges to surface waters. We assessed changes in soil test phosphorus (P) of the Ap horizon of cropped fields continuously irrigated for 26 yr with secondary effluent from the Penn State University wastewater treatment plant. For annual P additions averaging 97 kg P ha(-1), Mehlich-3 P (M3P) response in the 0- to 20-cm surface soil (initially < 20 mg kg(-1)) was represented by two lines. For the first 12 yr of irrigation, soil test P increased, with 14.5 kg P ha(-1) needed to increase M3P by 1 mg P kg(-1). After the initial buildup, M3P maintained a quasi-steady-state value of approximately 110 mg kg(-1). Over time, the surface soil equilibrium P concentration at zero sorption increased markedly (from < 1 to 5.5 mg P L(-1)), and extractable aluminum (Al) decreased significantly (P < 0.001). Speciation modeling using Visual MINTEQ suggests complexation of Al by dissolved organic carbon at site pH conditions. Loss of Al from the surface layer lowered its P-sorbing capacity, causing added effluent-P to move into the subsoil. Results suggest that current management practices can continue for many years without exceeding the surface soil M3P environmental threshold (200 mg kg(-1)) used in state P-based nutrient policies.     

Fate of atrazine in sandy soil cropped with sorghum

A field study was conducted to determine the fate of atrazine (6-chloro-N2-ethyl-N4-isopropyl-1,3,5-triazine-2,4-diamine) within the root zone (0 to 90 cm) of a sandy soil cropped with sorghum [Sorghum bicolor (L.) Moench] in Gainesville, Florida. Atrazine was uniformly applied at a rate of 1.12 kg ai. ha(-1) to a sorghum crop under moderate irrigation, optimum irrigation, and no irrigation (rainfed), 2 d after crop emergence. Bromide as a tracer for water movement was applied to the soil as NaBr at a rate of 45 kg Br ha(-1), 3 d before atrazine application. Soil water content, atrazine, and Br concentrations were determined as a function of time using soil samples taken from the root zone. Atrazine sorption coefficients and degradation rates were determined by depth for the entire root zone in the laboratory. Atrazine was strongly adsorbed within the upper 30 cm of soil and most of the atrazine recovered from the soil during the growing season was in that depth. The estimated half-life for atrazine was 32 d in topsoil to 83 d in subsoil. Atrazine concentration within the root zone decreased from 0.44 kg ai. ha(-1) 2 days after application (DAA) to 0.1 kg a.i. ha(-1) 26 DAA. Negligible amounts of atrazine (approximately 5 microg kg(-1)) were detected below the 60-cm soil depth by 64 DAA. Most of the decrease in atrazine concentration in the root zone over time was attributed to degradation. In contrast, all applied bromide had leached past the 60-cm soil depth during the same time interval.     

Biosolids affect soil barium in a dryland wheat agroecosystem

In December 2003, the USEPA released an amended list of 15 "candidate pollutants for exposure and hazard screening" with regard to biosolids land application, including Ba. Therefore, we decided to monitor soil Ba concentrations from a dryland wheat (Triticum aestivum L.)-fallow agroecosystem experiment. This experiment received 10 biennial biosolids applications (1982-2003) at rates from 0 to 26.8 dry Mg ha(-1) per application year. The study was conducted on a Platner loam (Aridic Paleustoll), approximately 30 km east of Brighton, CO. Total soil Ba, as measured by 4 M HNO(3), increased with increasing biosolids application rate. In the soil-extraction data from 1988 to 2003, however, we observed significant (P < 0.10) linear or exponential declines in ammonium bicarbonate-diethylenetriaminepentaacetic acid (AB-DTPA) extractable Ba concentrations as a function of increasing biosolids application rates. This was observed in 6 of 7 and 3 of 7 yr for the 0- to 20- and 20- to 60-cm soil depths, respectively. Results suggest that while total soil Ba increased as a result of biosolids application with time, the mineral form of Ba was present in forms not extractable with AB-DTPA. Scanning electron microscopy using energy dispersive spectroscopy verified soil Ba-S compounds in the soil surface, probably BaSO(4). Wet chemistry sequential extraction suggested BaCO(3) precipitation was increasing in the soil subsurface. Our research showed that biosolids application may increase total soil Ba, but soil Ba precipitates are insoluble and should not be an environmental concern in similar soils under similar climatic and management conditions.     

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.     

Soil microbial communities and enzyme activities under various poultry litter application rates

The potential excessive nutrient and/or microbial loading from mismanaged land application of organic fertilizers is forcing changes in animal waste management. Currently, it is not clear to what extent different rates of poultry litter impact soil microbial communities, which control nutrient availability, organic matter quality and quantity, and soil degradation potential. From 2002 to 2004, we investigated the microbial community and several enzyme activities in a Vertisol soil (fine, smectitic, thermic, Udic Haplustert) at 0 to 15 cm as affected by different rates of poultry litter application to pasture (0, 6.7, and 13.4 Mg ha(-1)) and cultivated sites (0, 4.5, 6.7, 9.0, 11.2, and 13.4 Mg ha(-1)) in Texas, USA. No differences in soil pH (average: 7.9), total N (pasture: 2.01-3.53, cultivated: 1.09-1.98 g kg(-1) soil) or organic C (pasture average: 25-26.7, cultivated average: 13.9-16.1 g kg(-1) soil) were observed following the first four years of litter application. Microbial biomass carbon (MBC) and nitrogen (MBN) increased at litter rates greater than 6.7 Mg ha(-1) (pasture: MBC = >863, MBN = >88 mg kg(-1) soil) compared to sites with no applied litter (MBC = 722, MBN = 69 mg kg(-1) soil). Enzyme activities of C (beta-glucosidase, alpha-galactosidase, beta-glucosaminidase) or N cycling (beta-glucosaminidase) were increased at litter rates greater than 6.7 Mg ha(-1). Enzyme activities of P (alkaline phosphatase) and S (arylsulfatase) mineralization showed the same response in pasture, but they were only increased at the highest (9.0, 11.2, and 13.4 Mg ha(-1)) litter application rates in cultivated sites. According to fatty acid methyl ester (FAME) analysis, the pasture soils experienced shifts to higher bacterial populations at litter rates of 6.7 Mg ha(-1), and shifts to higher fungal populations at the highest litter application rates in cultivated sites. While rates greater than 6.7 Mg ha(-1) provided rapid enhancement of the soil microbial populations and enzymatic activities, they result in P application in excess of crop needs. Thus, studies will continue to investigate whether litter application at rates below 6.7 Mg ha(-1), previously recommended to maintain water quality, will result in similar improved soil microbial and biochemical functioning with continued annual litter application.     

Recovery and distribution of biosolids-derived trace metals in a clay loam soil

The long-term mobility of trace metals has been cited as a potential hazard by critics of EPA 503 rule governing the land application of biosolids. The objectives of this study were to assess the accumulation of Cu, Ni, Cd, and Zn within the soil profile; the distribution of exchangeable, specifically adsorbed, organic, and oxide fractions of each metal; and mass balance of Cu, Ni, and Zn 17 yr after a single biosolids application. Biosolids were applied to 1.5- x 2.3-m confined plots of a Davidson clay loam (fine, kaolinitic, thermic Rhodic Kandiudult) in 1984 at 0, 42, 84, 126, 168, and 210 Mg ha(-1). The highest biosolids application supplied 4.5, 750, 43, and 600 kg ha(-1) of Cd, Cu, Ni, and Zn, respectively. Soils were sampled to a depth of 0.9 m and sectioned into 5-cm increments after separating the Ap horizon. Total (EPA-3050B), bioavailable (Mehlich-I), sequential extraction, and dispersible clay analyses were performed on samples from the control, 126 Mg ha(-1), and 210 Mg ha(-1) treatments. Trace metals are still concentrated in the top 0.2 m with slight enrichment down to 0.3 m. More than 85% of applied Cu, Ni, and Zn are still found in the topsoil where biosolids was incorporated and 95% or more of the applied metals were accounted for with mass balance calculations. Mehlich-I results showed a slight increase in metal concentration down to 0.35 m. Biosolids application increased the concentrations of trace metals in all the extracted fractions. The major portions of Cu, Zn, and Ni are associated with the metal-oxides fraction. Dispersible clay content and water-soluble metal contents were low and except for water-soluble Zn they were not affected by biosolids application. Results from this study showed that 17 yr after biosolids application there was negligible movement of trace metals through the soil profile and consequently there is little risk of contamination of ground water at this site.