Leachate chemistry of field-weathered spent mushroom substrate

Passive leaching by rainfall and snowmelt is a popular method to treat piles of spent mushroom substrate (SMS) before its reuse. During this field weathering process, leachate percolates into the underlying soils. A field study was conducted to examine the chemistry of SMS leachate and effects of infiltration. Two SMS piles were deposited (90 and 150 cm in height) over a Typic Hapludult and weathered for 24 mo. Leachate was collected biweekly using passive capillary samplers. The SMS leachate contained high concentrations of dissolved organic carbon (DOC; 0.8-11.0 g L(-1)), dissolved organic nitrogen (DON; 0.1-2 g L(-1)), and inorganic salts. The pH, electrical conductivity, and acid neutralizing capacity were 6.6 to 9.0, 21 to 66 ds m(-1), and 10 to 75 mmolc L(-1), respectively. Inorganic chemistry of the leachate was dominated by K+, Cl-, and SO24-. Leachate DOC was predominantly low molecular weight (<1000 Da) organic acids. During 2 yr of weathering, the 90-cm SMS pile released (per cubic meter of SMS) 3.0 kg of DOC, 1.6 kg of dissolved N, and 26.6 kg of inorganic salts. The 150-cm pile released (per cubic meter of SMS) 2.8 kg of DOC, 0.7 kg of dissolved N, and 13.6 kg of inorganic salts. The 150 cm pile retained more water and exhibited lower net nitrification compared with the 90-cm pile. The top 90 cm of soil retained 20 to 89% of the leachate solutes. Weathering of SMS in piles of 90 cm depth or greater may adversely affect ground water quality.     

Dissolved organic carbon fluxes under bare soil

The flux of dissolved organic carbon (DOC) in soil facilitates transport of nutrients and contaminants in soil. There is little information on DOC fluxes and the relationship between DOC concentration and water flux in agricultural soils. The DOC fluxes and concentrations were measured during 2.5 yr using 30 automatic equilibrium tension plate lysimeters (AETPLs) at 0.4 m and 30 AETPLs at 1.20-m depth in a bare luvisol, previously used as an arable soil. Average annual DOC fluxes of the 30 AETPLS were 4.9 g C m(-2) y(-1) at 0.4 m and 2.4 g C m(-2) y(-1) at 1.2 m depth. The average leachate DOC concentrations were 17 mg C L(-1) (0.4 m) and 9 mg C L(-1) (1.2 m). The DOC concentrations were unrelated to soil moisture content or average temperature and rarely dropped below 9 mg C L(-1) (0.4 m) and 5 mg C L(-1) (1.2 m). The variability in cumulative DOC fluxes among the plates was positively related to leachate volume and not to average DOC concentrations at both depths. This suggests that water fluxes are the main determinants of spatial variability in DOC fluxes. However, the largest DOC concentrations were inversely proportional to the mean water velocity between succeeding sampling periods, suggesting that the maximal net DOC mobilization rate in the topsoil is limited. Elevated DOC concentrations, up to 90 mg C L(-1), were only observed at low water velocities, reducing the risks of DOC-facilitated transport of contaminants to groundwater. The study emphasizes that water flux and velocity are important parameters for DOC fluxes and concentrations.     

Temperature and microbial activity effects on trace element leaching from metalliferous peats

Due to geochemical processes, peat soils often have elevated concentrations of trace elements, which are gradually released following drainage for agriculture. Our objectives were to use incubation temperatures to vary microbial activity in two metalliferous peats (M7 acidic peat and M3 neutral peat) from the Elba, New York region, and to use periodic leaching to assess the extent of trace element release from these soils. Dried soils were mixed with glass beads to maintain aeration, moistened, and incubated at 4, 16, 28, and 37 degrees C in 10-cm-diameter x 8-cm-tall columns. Five incubation-leaching cycles were performed, each consisting of 7.3 d of incubation (28 d for the final cycle) followed by 16 h of leaching with synthetic acid rain at 2.5 mm h(-1). Microbial activity was determined initially and after the final leaching by measuring C mineralization following glucose stimulation. Cumulative respiration results were ranked 28 > 16 > 4 > 37 degrees C, with M7 acidic peat respiration values greater than M3 neutral peat at each temperature. Initial leachate pH levels were between 2 and 4, with acidification less pronounced and shorter-lived for the M3 peat. Leachate S, dissolved organic carbon (DOC), NO3-N, and trace elements declined with successive leachings (rebounding slightly in the final M3 leachate), with concentrations typically greater in the M7 leachate. Elemental losses followed the same general ranking (28 > 16 > 4 > 37 degrees C); losses at 28 degrees C were 15 to 22% for As, Cd, Ni, and Zn from the M7 peat; losses from M3 were comparable only for Cu (1%) and Ni (19%). The correlation of respiration with S, DOC, and trace elements losses indicates that microbial processes mediated the release of trace elements in both peat soils. Neutral M3 peat pH levels limited losses of most analytes.     

Nutrient and trace element leaching following mine reclamation with biosolids

Mine reclamation with biosolids increases revegetation success but nutrient addition well in excess of vegetation requirements has the potential to increase leaching of NO3 and other biosolids constituents. A 3-yr water quality monitoring study was conducted on a Pennsylvania mine site reclaimed with biosolids applied at the maximum permitted and standard loading rate of 134 Mg ha(-1). Zero-tension lysimeters were installed at 1-m depth 1 yr before reclamation: three in the biosolids application area, one in a control area (no biosolids). Before reclamation, all water samples had pH in the range 4.7 to 6.2, acidity < 20 mg L(-1), and very low levels of all other measured parameters. Following reclamation, percolate water in the biosolids-treated area had lower pH and greater acidity than the control area. Acidity was greatest during the first winter following biosolids application, decreased during the spring, and showed a similar pattern but with much smaller concentrations the second year. Maximum first- year leachate NO3 concentrations were approximately 300 mg L(-1) and half as large the second year. Estimated inorganic N leaching loss during the first 2 yr after biosolids application was 2327 kg N ha(-1). Aluminum, Mn, Cu, Ni, Pb, and Zn followed similar leaching patterns as did acidity, and their mobilization appeared to be the result of the increased acidity. These results indicate that large applications of low-C/N-ratio biosolids could negatively impact area water quality and that biosolids reclamation practices should be modified to reduce this possibility.     

Accelerated weathering of biosolid-amended copper mine tailings

Application of municipal biosolids to mine tailings can enhance revegetation success, but may cause adverse environmental impacts, such as increased leaching of NO3- and metals to ground water. Kinetic weathering cells were used to simulate geochemical weathering to determine the effects of biosolid amendment on (i) pH of leachate and tailings, (ii) leaching of NO3- and SO4(2-), (iii) leaching and bioavailability (DTPA-extractable) of selected metals, and (iv) changes in tailing mineralogy. Four Cu mine tailings from southern Arizona differing in initial pH (3.3-7.3) and degree of weathering were packed into triplicate weathering cells and were unamended and amended with two rates (equivalent to 134 and 200 Mg dry matter ha(-1)) of biosolids. Biosolid application to acid (pH 3.3) tailings resulted in pH values as high as 6.3 and leachate pH as high as 5.7, and biosolids applied to circumneutral tailings resulted in no change in tailing or leachate pH. Concentrations of NO3--N of up to 23 mg L(-1) occurred in leachates from circumneutral tailings. The low pH of the acidic tailing apparently inhibited nitrification, resulting in leachate NO3--N of <5 mg L(-1). Less SO4(2-)-S was leached in biosolid-amended versus unamended acid tailings (final rate of 0.04 compared with 0.11 g SO4(2-)-S wk(-1)). Copper concentrations in leachates from acidic tailings were reduced from 53 to 27 mg L(-1) with biosolid amendment. Copper and As concentrations increased slightly in leachates from biosolid-amended circumneutral tailings. Small increases in DTPA-extractable Cu, Ni, and Zn occurred in all tailings with increased biosolid rate. Overall, there was little evidence of potential for adverse environmental impacts resulting from biosolid application to these Cu mine tailings.     

The effects of throughfall manipulation on soil leaching in a deciduous forest

The effects of changing precipitation on soil leaching in a deciduous forest were examined by experimentally manipulating throughfall fluxes in the field. In addition to an ambient treatment (AMB), throughfall fluxes were reduced by 33% (DRY treatment) and increased by 33% (WET treatment) using a system of rain gutters and sprinklers on Walker Branch Watershed, Tennessee. Soil leaching was measured with resin lysimeters in the O horizons and with ceramic cup lysimeters in the E (25 cm) and Bt (70 cm) horizons. Large and statistically significant treatment effects on N fluxes were found in the O horizons (lower N fluxes in the DRY and higher N fluxes in the WET treatment). Together with the greater O horizon N content observed in the DRY treatment, this suggested that N was being immobilized at a greater rate in the DRY treatment than in the AMB or WET treatments. No statistically significant treatment effects on soil solution were found in the E horizons with the exception of (Ca2+ + Mg2+) to K+ ratio. Statistically significant treatment effects on electrical conductivity (EC), pH, Ca2+, Mg2+, K+, Na+, SO4(2-), and Cl- were found in the Bt horizons due to differences between the DRY and other treatments. Despite this, calculated fluxes of Ca2+, Mg2+, K+, Na+, SO4(2-), and Cl- were lowest in the DRY treatment. These results suggest that lower precipitation will cause temporary N immobilization in litter and long-term enrichment in soil base cations whereas increased precipitation will cause long-term depletion of soil base cations.     

Phosphorus leaching from cow manure patches on soil columns

The loss of P in overland flow or leachate from manure patches can impair surface water quality. We studied leaching of P from 10-cm-high lysimeters filled with intact grassland soil or with acid-washed sand. A manure patch was created on two grassland and two sand-filled lysimeters, and an additional two grass lysimeters served as blanks. Lysimeters were leached in the laboratory during 234 d with a diluted salt solution, and column effluent was passed through a 0.45-microm filter, analyzed for pH, dissolved reactive P (DRP), and total dissolved P (TDP). At the end of the experiment lysimeter soil was sampled and analyzed for pH, available P, and oxalate-extractable P, Fe, and Al. The concentration of TDP in the effluent from the sand column increased to 25 mg L-1 during the first weeks and remained above 10 mg L-1 during the rest of the percolation. In effluent from grass + patch lysimeters TDP gradually increased to 4 mg L-1. Both in the manure and in the effluent of the sand lysimeter P was found mainly in the form of DRP, but in the effluent from the grass lysimeters was found mainly as dissolved unreactive P (DUP=TDP-DRP). Earthworm activity was responsible for decomposition of the manure patch on the grass lysimeters. Manure patches and their remains were found to be a long-term source of high concentrations of P in leachates. Spreading of patches after a grazing period could reduce their possible negative impacts on the environment.     

Sorption and fractionation of dissolved organic matter and associated phosphorus in agricultural soil

Mobility of dissolved organic matter (DOM) strongly affects the export of nitrogen (N) and phosphorus (P) from soils to surface waters. To study the sorption and mobility of dissolved organic C and P (DOC, DOP) in soil, the pH-dependent sorption of DOM to samples from Ap, EB, and Bt horizons from a Danish agricultural Humic Hapludult was investigated and a kinetic model applicable in field-scale models tested. Sorption experiments of 1 to 72 h duration were conducted at two pH levels (pH 5.0 and 7.0) and six initial DOC concentrations (0-4.7 mmol L(-1)). Most sorption/desorption occurred during the first few hours. Dissolved organic carbon and DOP sorption decreased strongly with increased pH and desorption dominated at pH 7, especially for DOC. Due to fractionation during DOM sorption/desorption at DOC concentrations up to 2 mmol L(-1), the solution fraction of DOM was enriched in P indicating preferred leaching of DOP. The kinetics of sorption was expressed as a function of how far the solution DOC or DOP concentrations deviate from "equilibrium." The model was able to simulate the kinetics of DOC and DOP sorption/desorption at all concentrations investigated and at both pH levels making it useful for incorporation in field-scale models for quantifying DOC and DOP dynamics.     

南充市近十年酸雨变化特征及降水化学组成研究

依据南充市2003~2012年城区降水环境监测统计资料,分析了酸雨变化特征及降水离子化学组成。研究表明:这十年,酸雨频率平均为50.4%,2007年降雨量为最高,呈波动递减趋势变化,降水年平均pH值为4.88,呈现"低—高—低"的变化特征,城区酸雨频率和降水pH值月均值变化呈现高低交替的波动趋势。城区降水中主要阳离子成分是Ca2+,主要阴离子成分是SO2-4和NO-3。(SO2-4/NO-3)比值逐年下降,平均比值为7.82,酸雨污染类型仍以硫酸型为主;降水(NH+4+Ca2+)/(SO2-4+NO-3)和Ca2+/NH+4比值呈波动性变化,2007年分别达到最高值为6.71和50.27,除2010年比值均较低小于1外,近年来均有增加趋势,表明碱性离子缓冲能力增强了,降水酸度降低,pH值增加,但2007年pH值较低,主要与降雨量有关。综合分析,降水酸度不仅是酸性离子和碱性离子中和作用,也受其他离子浓度和降雨量、风向等气候条件、距离传输以及地形等影响。     

Chemical analysis of soil and leachate from experimental wetland mesocosms lined with coal combustion products

Small-scale (1 m2) wetland mesocosm experiments were conducted over two consecutive growing seasons to investigate the effects on soil and leachate chemistry of using a recycled coal combustion product as a liner. The coal combustion product used as a liner consisted of flue gas desulfurization (FGD) by-products and fly ash. This paper provides the chemical characteristics of mesocosm soil and leachate after 2 yr of experimentation. Arsenic, Ca, and pH were higher in FGD-lined mesocosm surface soil relative to unlined mesocosms. Aluminum was higher in the soils of unlined mesocosms relative to FGD-lined mesocosms. No significant difference of potentially phytotoxic B was observed between lined and unlined mesocosms in the soil. Higher pH, conductivity, and concentrations of Al, B, Ca, K, and S (SO4-S) were observed in leachate from lined mesocosms compared with unlined controls while Fe, Mg, and Mn were higher in leachate from unlined mesocosms. Concentrations of most elements analyzed in the leachate were below national primary and secondary drinking water standards after 2 yr of experimentation. Initially high pH and soluble salt concentrations measured in the leachate from the lined mesocosms may indicate the reason for early effects noted on the development of wetland vegetation in the mesocosms.     

Sorption of trace metals by standard and micro suction cups in the absence and presence of dissolved organic carbon

Both the bioavailability of a trace metal (TM) in a soil and the risk of leaching to the ground water are linked to the metals concentration in the soil solution. Sampling soil solution by tension lysimetry with suction cups is a simple and established technique that is increasingly used for monitoring dissolved TM in soils. Of major concern, however, is the sorption of TM by the walls of the samplers. Metal sorption by different materials used in suction cups can vary widely, depending also on the chemistry of the soil solution. We compared the sorption of Cu, Zn, Cd, and Pb by different standard-size and micro suction cups in the laboratory at two pH values (4.5 and 7.5 or 8.0) in absence and presence of dissolved organic carbon (DOC). In addition, we investigated the sorption of DOC from different origins by the cup materials. At both pH values, the weakest sorption of all four TMs was exhibited by standard-size suction cups based on nylon membranes and by hollow fibers made from polyvinyl alcohol (PVA). At alkaline pH, borosilicate glass, ceramic materials, and polytetrafluorethylene (PTFE) mixed with silicate were characterized by generally strong sorption of all investigated TMs. In addition, Cu and Pb were strongly sorbed at low pH by PTFE-silicate and a ceramic material used for the construction of standard-size suction cups. On the other hand, sorption of Cu, Zn, and Cd by ceramic capillaries produced from pure aluminum oxide was negligible at low pH. Micro suction cups made of an unknown polymerous tube sorbed Cu strongly, but were well suited to monitor Zn, Cd, and Pb at low pH, and, in the presence of DOC, also at high pH. Major cations (Na+, Mg2+, K+, Ca2+) and anions (Cl-, NO3-, SO4(2-)) were not or very weakly sorbed by all cup materials, except for Mg2+, K+, and Ca2+ by borosilicate glass at pH 7.5. Trace metal sorption by suction cups was generally greatly reduced in the presence of DOC, especially at alkaline pH. The sorption of DOC itself depended on its source. Dissolved organic carbon from leaf litter extracts with a probably large hydrophobic fraction was sorbed more strongly than mainly hydrophilic DOC from a mineral soil solution.     

Fly ash and lime-stabilized biosolid mixtures in mine spoil reclamation: simulated weathering

The use of large quantities of neutral coal fly ash (NFA) may be facilitated by co-application with a lime-stabilized biosolid (LSB) for the reclamation of acid mine spoil (AMS). Although NFA may not aid in the mitigation of acid drainage, questions concerning the leachability and mineralogy of native and NFA- and LSB-born metals must be addressed. In this study, the potential long-term influence of LSB and NFA on AMS leachate chemistry and trace element mineralogy was evaluated using laboratory weathering and selective dissolution techniques. The application of LSB at a rate sufficient to neutralize the potential acidity of the AMS increased leachate pH from approximately 3 to 7.5 for the duration of the study. Fly ash rates (1X, 1.5X, and 2X LSB rate) did not affect leachate pH. The dominant electrolytes in all leachates were Ca and SO4, the concentrations of which were mirrored by solution electrical conductivity (EC). Leachate concentrations of Al, Fe, Mn, K, Cu, Ni, and Zn were significantly reduced by LSB application, whereas concentrations of Ca, SO4, Mg, Cl, F, B, and P were increased. Nitrate concentrations were not affected by LSB. With the exception of leachate B, which increased with increasing NFA rate and was regenerated during the weathering study, NFA did not affect leachate composition. Sequential selective dissolution indicated a transformation of Co, Cr, Cu, Ni, Pb, and Zn into less labile mineral pools with weathering. The results of these evaluations suggest that the application of NFA during AMS reclamation would have little effect on leachate chemistry or the mineralogy of trace elements. Thus, the high-volume application of NFA to AMS during reclamation may offer an additional opportunity for the use of this combustion by-product.     

Coupled effects of treated effluent irrigation and wetting-drying cycles on transport of triazines through unsaturated soil columns

The physical and chemical parameters controlling the movement of atrazine (6-chloro-N2-ethyl-N4-isopropyl-l,3,5-triazine-2,4-diamine; 98.8%) and prometryn [N,N'-bis(1-methylethyl)-6-(methylthio)-l,3,5triazine-2,4-diamine; 99.5%] were investigated in columns infiltrated with treated effluent under unsaturated transient conditions and subjected to drying events at 22 or 60 degrees C followed by rewetting. Three soils varying in soil pH and texture and three solutions were used. The infiltrating solutions consisted of either a CaCl2 matrix (CC), a swine waste-derived lagoon effluent (SW), or a simulated buffer solution (SB) representative of the element composition and pH of the SW but with no dissolved organic matter. Several parameters were monitored including leachate triazine concentrations, pH, dissolved organic carbon (DOC), inorganic carbon, and flow rates. Compared with CC, application of SW and SB increased column leachate pH, enhanced dissolution of organic carbon and particle dispersion, and decreased average flow rates, which allowed for increased desorption time. The coupled effect of these processes enhanced movement of triazines in some cases, with SW generally having the greatest effect. The individual effect of increased pH was more pronounced for prometryn (pKa=4.05) versus atrazine (pKa=1.66), and most dramatic for the soil with the lowest initial pH. High-temperature drying, which simulated intensive evaporation, further enhanced the dissolution of soil organic matter and the reduction in leachate flow rates with SW and SB applications; however, the net effect under the experimental conditions employed varied with soil type. Relative to low-temperature drying, high-temperature drying in the silty clay loam-packed columns reduced pesticide migration.     

成都市郊区雾水中阴离子变化的研究

本文用冷凝法采集雾水样品,用离子色谱法测定雾水样品中阴离子(氟离子、氯离子、亚硝酸根离子、硝酸根离子、硫酸根离子)的浓度,研究表明雾水中阴离子浓度与雾的浓密有关,雾水中硫酸根离子含量最高;雾水中阴离子浓度随大雾的消失而降低;雾水中阴离子浓度大于雨水。所得结果对在大雾天气情况下保护人体健康有一定参考意义。     

Ryegrass cover crop effects on nitrate leaching in spring barley fertilized with 15NH415NO3

Cover crops are a management option to reduce NO3 leaching under cereal grain production. A 2-yr field lysimeter study was established in Uppsala, Sweden, to evaluate the effect of a perennial ryegrass (Lolium perenne L.) cover crop interseeded in barley (Hordeum vulgare L.) on NO3-N leaching and availability of N to the main crop. Barley and ryegrass or barley alone were seeded in mid-May 1992, in lysimeters (03-m diam. x 1.2-m depth) of an undisturbed, well-drained, sandy loam soil. Fertilizer N was applied at the same time as labeled l5NH415NO3 (10 atom % 15N) at a rate of 100 kg N ha(-1). In 1993, barley was reseeded in May in the lysimeters but with nonlabeled NH4NO3 and no cover crop (previous year's cover crop incorporated just prior to seeding). Barley yields and total and fertilizer N uptake in Year 1 (1992) were unaffected by cover crop. Total aboveground N uptake by the ryegrass was 28 kg ha(-1) at the time of incorporation the following spring. Recovery of fertilizer-derived N in May 1993 was about 100%; 53% in soil, 46% in barley, <2% in ryegrass, and negligible amounts in leachate. In May 1994, the corresponding figures were: 32% in soil, <3% in barley, and, again, negligible amounts in leachate. The cover crop reduced concentrations of NO3-N in the leachate considerably (<5 mg L(-1), compared with 10 to 18 mg L(-1) without cover crop) at most sampling times from November 1992 to April 1994, and reduced the total amount of NO3-N leached (22 compared with 8 kg ha(-1)).     

NITROGEN CONTENT AND ACIDITY OF RAIN ON THE GEORGIA COAST1

ABSTRACT: Since nitrogen is a nutrient frequently in short supply in coastal ecosystems, an estimate of the nitrogen input via rain was made for the Georgia coast. Water samples collected in 34 separate storms during a 12 month period were analysed for concentrations of ammonia, nitrate plus nitrite, and dissolved organic nitrogen (DON). The range and average concentration in micromoles of nitrogen per liter was 0.0 to 137 (6.3) for ammonia, 1.0 to 21 (7.9) for nitrate plus nitrite, and 0.0 to 13.6 (4.0) for DON. DON, not usually measured in rain, comprised up to 62% of the total nitrogen content. The annual amount of nitrogen contributed by rain to the coast was about 0.3 g N/m². This value is a small fraction of the calculated nitrogen requirements of coastal plants. More than half the rain samples had pH values less than the CO₂ equilibrium pH of 5.6. Values as low as 4.2 were in the range of pH values reported for acid rain in Europe and the northeastern U.S. Total titratable acidity was measured for 12 summer rainwater samples. The results fox 7 individual storms showed a highly linear relation between hydrogen ion concentration and total acidity. However, the elope of the regression line indicated that increases in acidity were not a result of addition of strong acid alone.     

Role of organic matter in microbial transport during irrigation with sewage effluent

Reduction of migration of fecal coliforms (FC) and streptococci (FS) by limiting the leaching in effluent-irrigated soil was tested in lysimeters packed with quartz sand without or with added biosolids compost or with one of two clayey soils. The 200-L, 70-cm-deep lysimeters were either planted with a Eucalyptus camaldulensis or an Oroblanco citrus tree (in the sand only), or not planted. The Eucalyptus was irrigated with oxidation pond effluent (OPE) and the Oroblanco with mechanical-biological treatment plant effluent (MBTPE). The leaching fraction (LF) ranged from 0.2 to about 1.0, and the residence time (RT) from under 1 to 40 d. The Eucalyptus was also tested under intermittent leaching (RT 11-20 d) and deficit irrigation (without leaching for about 6 mo) regimes. Under MBTPE irrigation there was little or no leaching of FC and FS. Under OPE irrigation at LF 1 without a Eucalyptus there was little or no bacterial leaching at irrigation rates below 40 L d(-1) per lysimeter (RT > or = 0.8 d). Bacterial counts in the leachate were substantial in the presence of a Eucalyptus tree under LF 0.2 and intermittent leaching regimes, and when sand-packed unplanted lysimeters received OPE effluent at >45 L d(-1). Bacterial recovery peaked at LF 0.2, at up to 45% of the input level. At LF 1 (RT 0.6-2.8 d) and with intermittent leaching the recoveries were minute. Bacterial counts in the washout from the deficit-irrigated lysimeters were typical of nonpolluted soils. The bacterial concentration and recovery patterns in the leachate mostly matched the organic carbon (OC) load in the irrigation water, and its concentration and bioavailablity in the leachate. We related the leaching patterns of the fecal bacteria to their relative reproduction and die-off rates, and to the dependence of their regrowth on available carbon sources.     

Determining sources of dissolved organic carbon and disinfection byproduct precursors to the McKenzie River, Oregon

This study was conducted to determine the main sources of dissolved organic carbon (DOC) and disinfection byproduct (DBP) precursors to the McKenzie River, Oregon (USA). Water samples collected from the mainstem, tributaries, and reservoir outflows were analyzed for DOC concentration and DBP formation potentials (trihalomethanes [THMFPs] and haloacetic acids [HAAFPs]). In addition, optical properties (absorbance and fluorescence) of dissolved organic matter (DOM) were measured to provide insight into DOM composition and assess whether optical properties are useful proxies for DOC and DBP precursor concentrations. Optical properties indicative of composition suggest that DOM in the McKenzie River mainstem was primarily allochthonous--derived from soils and plant material in the upstream watershed. Downstream tributaries had higher DOC concentrations than mainstem sites (1.6 +/- 0.4 vs. 0.7 +/- 0.3 mg L(-1)) but comprised < 5% ofmainstem flows and had minimal effect on overall DBP precursor loads. Water exiting two large upstream reservoirs also had higher DOC concentrations than the mainstem site upstream of the reservoirs, but optical data did not support in situ algal production as a source of the added DOC during the study. Results suggest that the first major rain event in the fall contributes DOM with high DBP precursor content. Although there was interference in the absorbance spectra in downstream tributary samples, fluorescence data were strongly correlated to DOC concentration (R2 = 0.98), THMFP (R2 = 0.98), and HAAFP (R2 = 0.96). These results highlight the value of using optical measurements for identifying the concentration and sources of DBP precursors in watersheds, which will help drinking water utilities improve source water monitoring and management programs.     

Nitrogen and carbon leaching in agroecosystems and their role in denitrification potential

The drainage of water and leaching of dissolved constituents represent major components of agroecosystem mass budgets that have been exceedingly difficult to measure. Equilibrium-tension lysimeters (ETLs) were used to monitor drainage, nitrogen (N), and carbon (C) leaching through Plano silt loam (fine-silty, mixed, superactive, mesic Typic Argiudoll) for a 4-yr period in a restored prairie and N-fertilized no-tillage and chisel-plowed maize (Zea mays L.) agroecosystems. Mean drainage recorded during 4 yr for the prairie, no-tillage, and chisel-plowed ecosystems totaled 461, 1,116, and 1,575 mm and represented 16, 33, and 47% of precipitation plus melting of drifted snow received, respectively. Total inorganic N leaching losses during the 4-yr period for the prairie, no-tillage, and chisel-plowed ecosystems were 0.6, 201, and 179 kg N ha(-1), respectively. Inorganic N leaching represented 26 and 24% of applied fertilizer N additions to the no-tillage and chisel-plowed agroecosystems. Total dissolved C leaching losses were 119, 435, and 502 kg C ha(-1) for the prairie, no-tillage, and chisel-plowed ecosystems, respectively. Sufficient dissolved organic carbon (DOC) and nitrate N (NO3- -N) existed in the prairie and agroecosystems to support subsoil denitrification. Potential denitrification, however, was limited by insufficient lengths of saturated soil conditions in all three ecosystems, the supply of DOC in the agroecosystems, and the supply of nitrate N in the prairie. Based on available DOC and nitrate N, the maximum contribution of denitrification below the root zone in the agroecosystems was less than 25% of the total amount of leached nitrate N and the probable contribution of denitrification was much less.     

Effect of tomato packinghouse wastewater properties on phosphorus and cation leaching in a spodosol

Land application of wastewater is a common practice. However, coarse-textured soils and shallow groundwater in Florida present favorable conditions for leaching of wastewater-applied constituents. Our objective in this study was to determine phosphorus (P) and associated cations (Ca, Mg, K, Na) leaching in a Spodosol irrigated with tomato packinghouse wastewater. We packed 12 polyvinyl chloride soil columns (30 cm internal diameter × 50 cm length) with two soil horizons (Ap and A/E) and conducted 30 sequential leaching events by irrigating with wastewater at low (0.84 cm d), medium (1.68 cm d), and high (2.51 cm d) rates. The control treatment received deionized water at 1.68 cm d Leachate pH was lower (6.4-6.5) and electrical conductivity (EC) was higher in the wastewater-treated columns (0.85-1.78 dS m) than in the control treatment (pH 6.9; EC, 0.12 dS m) due to the low pH (6.2) and high EC (2.16 dS m) of applied wastewater. Mean leachate P concentrations were greatest in the control treatment (0.70 mg L), followed by the high (0.60 mg L) and low and medium wastewater-treated columns (0.28-0.33 mg L). Leachate concentrations of Na, Ca, Mg, and K were significantly ( < 0.05) greater in wastewater-treated columns than in the control. Concentrations of P, Na, and K in leachate remained lower than the concentrations in the applied wastewater, indicating their retention in the soil profile. In contrast, leachate Ca and Mg concentrations were greater than in applied wastewater during several leaching events, suggesting that additional Ca and Mg were leached from the soil. Our results suggest that tomato packinghouse wastewater can be beneficially land-applied at 1.68 cm d in Florida's Spodosols without significant P and cation leaching.