Trace element retention and release on minerals and soil in a constructed wetland

Constructed wetlands are one method under investigation for the remediation of trace element-contaminated agricultural drainwater. A greater understanding of the retention of trace elements by the bulk soil and soil constituents is necessary for their safe and effective use. To determine the capacity of soil, calcite, and goethite-coated quartz sand for retention of As, Mo, and V under field conditions, an in situ method was used whereby permeable bags containing those minerals were placed near the sediment surface of a flow-through constructed wetland for 3 or 12 mo. Accumulations of As, Mo, and V occurred on goethite-coated sand. Concentrations of Mo on goethite-coated sand were much higher in samples from a wetland cell with a water depth of 15 cm (38.23 +/- 7.27 mg kg(-1)) compared with those from a cell with a water depth of 3 cm (8.30 +/- 1.45 mg kg(-1)). Calcite sorbed no As and low amounts of Mo and V, indicating that it is not an important sink for those elements under these conditions. In soil bags, total As and V concentrations showed little change over 12 mo. Molybdenum accumulated in the soil bags, resulting in total concentrations (12 mo) of 27.22 +/- 2.69 mg kg(-1) and 11.42 +/- 1.35 mg kg(-1) at water depths of 15 and 3 cm, respectively. Nearly half of the Mo accumulation on soil became water soluble after air-drying. This has important implications for systems that may undergo changes in redox status, possibly resulting in large fluxes of water-soluble Mo.     

Nutrients and Heavy Metals in Legacy Sediments: Concentrations,Comparisons with Upland Soils,and Implications for Water Quality

Concentrations of nutrients and heavy metals in streambank legacy sediments are needed to estimate watershed exports and to evaluate against upland inputs. Concentrations of nutrients and heavy metals were determined for legacy sediments in 15 streambanks across northeastern Maryland, southeastern Pennsylvania, and northern Delaware. Samples were collected from multiple bank depths from forested, agricultural, urban, and suburban sites. Analyses were performed for fine (<63 μm) and coarse sediment fractions. Nutrient and heavy metal concentrations were significantly higher in fine than coarse legacy sediments and water extractable nutrient concentrations were significantly greater for fine sediments. Nutrient and heavy metal concentrations were highest in streambank legacy sediments associated with urban land use, but few differences were found with bank depth. Total N (40–3,970 mg/kg) and P (25–1,293 mg/kg) and bioavailable P (0.25–48.8 mg/kg) concentrations for legacy sediments were lower than those for upland soils. This suggests that legacy sediments could serve as sink or source of N and P depending on the redox conditions and stream water nutrient concentrations. However, despite low concentrations, caution should be exercised since streambank erosion and legacy sediment mass loadings could be high, these sediments are in immediate proximity of aquatic ecosystems, and biogeochemical transformations could result in release of the nutrients.     

Metal release from bottom sediments of Ocoee Lake No. 3, a primary catchment area for the Ducktown Mining District

Ocoee Lake No. 3 is the first reservoir receiving suspended sediments contaminated with trace metals discharged by acid mine effluents from the Ducktown Mining District, Tennessee. Bottom sediments (0-5 cm) from the lake were sampled to assess the potential for future adverse environmental effects if no remediation controls or activities are implemented. The sediments were found to include a major component (173 +/- 19 g kg(-1)) that dissolved in 6 mol L(-1) HCl within 24 h. This acid-soluble and relatively labile fraction contained high concentrations of Fe (460 +/- 40 g kg(-1)), Al (99 +/- 11 g kg(-1)), Mn (10 +/- 8 g kg(-1)), Cu (2000 +/- 700 mg kg(-1)), Zn (1300 +/- 200 mg kg(-1)), and Pb (300 +/- 200 mg kg(-1)). When the pH of water in contact with the sediment was decreased experimentally from 6.4 to 2.6, the concentrations of dissolved trace metals increased by factors of 2200 for Pb, 160 for Cu, 21 for Zn, 9 for Cd, 8 for Ni, and 5 for Co. The order in which metals were released with decreasing pH was the reverse of that reported for pH-dependent sorption of these metals in upstream systems. Substantial release of trace metals from the sediment was observed even by a modest decrease of pH from 6.4 to 5.9. Therefore, the metal-rich sediment of the lake should be considered as potentially hazardous to bottom-dwelling aquatic species and other organisms in the local food chain. In addition, if the reservoir is dredged or if the dam is removed, the accumulated sediment may have to be treated for recovery of sorbed metals.     

Occurrence of metals in soil and ground water near chromated copper arsenate-treated utility poles

To thoroughly investigate the metal contamination around chromated copper arsenate (CCA)/polyethylene glycol (PEG)-treated utility poles, a total of 189 soil samples obtained from different depths and distances near six treated poles in the Montreal area (Canada) were analyzed for Cu, Cr, and As content. Various soil physicochemical properties were also determined. Ground water samples collected below the poles were analyzed for metals and bioassays with Daphnia magna were conducted. Generally, sandy soils had lower contaminant levels than clayey and organic soils. Copper concentrations in soil were highest followed by As and Cr. The highest Cu (1460 +/- 677 mg kg(-1)), As (410 +/- 150 mg kg(-1)), and Cr (287 +/- 32 mg kg(-1)) concentrations were found at the ground line and immediately adjacent to the pole. Contaminant levels then decreased with distance, approaching background levels within 0.1 m from the pole for Cr and 0.5 m for Cu and As. Chromium and Cu levels generally approached background levels at a depth of 0.5 m. Average As content near the pole on all study sites was three to eight times higher than Quebec's Level C criterion (50 mg kg(-1)), although it dropped to 31 mg kg(-1) at 0.1 m. Results also showed that As persisted up to 1 m in soil depth (17-54 mg kg(-1)). Copper and Cr concentrations in ground water samples were always <1.000 mg L(-1) and <0.05 mg L(-1), respectively and Cr(VI) was <0.02 mg L(-1). One sample contained an As concentration >0.025 mg L(-1) but bioassays showed that, overall, ground water had a low ecotoxic potential.     

Patterns of short-term sedimentation in a freshwater created marsh

This study investigated different sedimentation measurement techniques and examined patterns of short-term sedimentation in two 1-ha replicate created freshwater marshes in central Ohio, USA. Short-term (one-year) sediment accumulation above feldspar, clay, glitter, and sand artificial marker horizons was compared at different water depths and distances from wetland inflow. A sediment budget was also constructed from turbidity and suspended sediment data for comparison with marker horizons. Glitter and sand marker horizons were the most successful for measuring sediment accumulation (81-100% marker recovery), while clay markers were completely unsuccessful. The sedimentation rate for both wetlands averaged 4.9 cm yr(-1) (36 kg m(-2) yr(-1)), and ranged from 1.82 to 9.23 cm yr(-1) (12.4 to 69.7 kg m(-2) yr(-1)). Sedimentation rates in deep, open water areas were significantly higher than in shallow, vegetated areas for both wetlands (t test, p < 0.05). However, observed sedimentation patterns may be attributed more to preferential flow through open water areas than to water depth or presence of vegetation. Contrary to the expected spatial distribution, sedimentation was highly variable within the wetlands, suggesting that bioturbation and turbulence may cause significant resuspension or that high hydrologic loads may distribute sediments throughout the basins. A sediment budget estimated sediment retention of approximately 740 g m(-2) yr(-1) per wetland (43% removal rate), yet gross sediment accumulation was 36,000 g m(-2) yr(-1) measured by marker horizons. These results suggest that erosive forces may have influenced sedimentation, but also may indicate problems with the sediment budget calculation methodology.     

Removal of organic matter and nitrogen from river water in a model floodplain

A significant improvement in river water quality cannot be expected unless nonpoint-source contaminants are treated in addition to the further treatment of point-source contaminants. If river water is sprayed over a floodplain, the consequent water filtration through the sediment profile can simultaneously remove organic matter and nitrogen in the water through aerobic and denitrifying reactions. This hypothesis was tested using lysimeters constructed from polyvinyl chloride (PVC) pipe (150 cm long, 15 cm in diameter) packed with loamy sand floodplain sediment. Water was applied to the top of the lysimeters at three different flow rates (48, 54, and 68 mm d(-1)). Concentrations of NO3 and dissolved oxygen (DO), chemical oxygen demand (COD), and redox potential (Eh) in the water were measured as functions of depth after the system reached steady states for both water flow and reactions. At the rate of 68.0 mm d(-1), a reducing condition for denitrification developed below the 5-cm depth due to the depletion of O2 by organic matter degradation in the surface oxidizing layer; Eh and DO were below 205 mV and 0.4 mg L(-1), respectively. At a depth of 70 cm, COD and NO3-N concentration decreased to 5.2 and 3.8 mg L(-1) from the respective influent concentrations of 17.1 and 6.2 mg L(-1). Most biodegradable organic matter was removed during flow and further removal of NO3 was limited by the lack of an electron donor (i.e., organic matter). These results indicate that the floodplain filtration technique has great promise for treatment of contaminated river water.     

Sediment amendment with Phoslock® in Clatto Reservoir (Dundee, UK): Investigating changes in sediment elemental composition and phosphorus fractionation

Lanthanum-modified bentonite clay (Phoslock(?) is a lake remediation tool designed to strip dissolved phosphorus (P) from the water column and increase the sediment P-sorption capacity. This study investigated short term alterations in sediment elemental composition and sediment P-fractions based on sediment cores taken 2 days before and 28 days following the application of 24 t of Phoslock? to a 9 ha, man-made reservoir. Following the application, sediment lanthanum (La) content increased significantly (p < 0.05; n = 4) in the top 8 cm of the sediment, thereby theoretically increasing sediment P-binding capacity on the whole reservoir scale by 250 kg. Mass balance calculations were used to estimate the theoretical binding of release-sensitive P (P(mobile); sum of 'labile P', 'reductant-soluble P' and 'organic P' fraction) by La across the top 4 cm and 10 cm depth of sediment. The amended mass of La in the sediment had the potential to bind 42% of P(mobile) present in the top 4 cm or 17% of P(mobile) present in the top 10 cm. However, with the exception of a significant increase (p<0.05; n=4) in the 'residual P' fraction in the top 2 cm, sediment P-fractions, including P(mobile,) did not differ significantly following the Phoslock? application. Experimental P-adsorption studies indicated P-saturation values for Phoslock? of 21,670 mg P kg?1 Phoslock?. Sequential extraction of P from saturated Phoslock? under laboratory conditions indicated that around 21% of P bound by Phoslock? was release-sensitive, while around 79% of bound P was unlikely to be released under reducing or common pH (5-9) conditions in shallow lakes. Applying Phoslock? is, therefore, likely to increase the P-sorption capacity of sediments under reducing conditions.     

Metal distribution and stability in constructed wetland sediment

The A-01 wetland treatment system (WTS) is a surface flow wetland planted with giant bulrush [Schoenoplectus californicus (C.A. Mey.) Palla] that is designed to remove Cu and other metals from the A-01 National Pollution Discharge Elimination System (NPDES) effluent at the Savannah River Site near Aiken, SC. Copper, Zn, and Pb concentrations in water were usually reduced 60 to 80% by passage through the treatment system. The Cu concentrations in the wetland sediments increased from about 4 to 205 and 796 mg kg(-1), respectively, in the organic and floc sediment layers in cell 4A over a 5-yr period. Metal concentrations were higher in the two top layers of sediment (i.e., the floc and organic layers) than in the deeper inorganic layers. Sequential extraction was used to evaluate remobilization and retention of Cu, Pb, Zn, Mn, and Fe in the wetland sediment. Metal remobilization was determined by the potentially mobile fraction (PMF) and metal retention by the recalcitrant factor (RF). The PMF values were high in the floc layer but comparatively low in the organic and inorganic layers. High RF values for Cu, Zn, and Pb in the organic and inorganic layers indicated that these metals were strongly bound in the sediment. The RF values for Mn were lower than for the other elements especially in the floc layer, indicating low retention or binding capacity. Retention of contaminants was also evaluated by distribution coefficient (Kd) values. Distribution coefficient (Kd) values were lower for Cu and Zn than for Pb, indicating a smaller exchangeable fraction for Pb.     

Removal and distribution of iron, manganese, cobalt, and nickel within a Pennsylvania constructed wetland treating coal combustion by-product leachate

A flow-through wetland treatment system was constructed to treat coal combustion by-product leachate from an electrical power station at Springdale, Pennsylvania. In a nine-compartment treatment system, four cattail (Typha latifolia L.) wetland cells (designated Cells 1 through 4) successfully removed iron (Fe) and manganese (Mn) from the inlet water; Fe and Mn concentrations were decreased by an average of 91% in the first year (May 1996-May 1997), and by 94 and 98% in the second year (July 1997-June 1998), respectively. Cobalt (Co) and nickel (Ni) were decreased by an average of 39 and 47% in the first year, and 98 and 63% in the second year, respectively. Most of the metal removed by the wetland cells was accumulated in sediments, which constituted the largest sink. Except for Fe, metal concentrations in the sediments tended to be greater in the top 5 cm of sediment than in the 5- to 10- or 10- to 15-cm layers, and in Cell 1 than in Cells 2, 3, and 4. Plants constituted a much smaller sink for metals; only 0.91, 4.18, 0.19, and 0.38% of the Fe, Mn, Co, and Ni were accumulated annually in the aboveground tissues of cattail, respectively. A greater proportion of each metal (except Mn) was accumulated in cattail fallen litter and submerged Chara (a macroalga) tissues, that is, 2.81, 2.75, and 1.05% for Fe, Co, and Ni, respectively. Considerably higher concentrations of metals were associated with cattail roots than shoots, although Mn was a notable exception.     

Uptake and release of phosphorus from overland flow in a stream environment

Phosphorus runoff from agricultural fields has been linked to fresh-water eutrophication. However, edge-of-field P losses can be modified by benthic sediments during stream flow by physiochemical processes associated with Al, Fe, and Ca, and by biological assimilation. We investigated fluvial P when exposed to stream-bed sediments (top 3 cm) collected from seven sites representing forested and agricultural areas (pasture and cultivated), in a mixed-land-use watershed. Sediment was placed in a 10-m-long, 0.2-m-wide fluvarium to a 3-cm depth and water was recirculated over the sediment at 2 L s(-1) and 5% slope. When overland flow (4 mg dissolved reactive phosphorus [DRP] and 9 mg total phosphorus [TP] L(-1)) from manured soils was first recirculated, P uptake was associated with Al and Fe hydrous oxides for sediments from forested areas (pH 5.2-5.4) and by Ca for sediments from agricultural areas (pH 6.5-7.2). A large increase (up to 200%) in readily available P NH4Cl fraction was noted. After 24 h, DRP concentration in channel flow was related to sediment solution P concentration at which no net sorption or desorption of P occurs (EPC0) (r2 = 0.77), indicating quasi-equilibrium. When fresh water (approximately 0.005 mg P L(-1) mean base flow DRP at seven sites) was recirculated over the sediments for 24 h, P release kinetics followed an exponential function. Microbial biomass P accounted for 34 to 43% of sediment P uptake from manure-rich overland flow. Although abiotic sediment processes played a dominant role in determining P uptake, biotic process are clearly important and both should be considered along with the location and management of landscape inputs for remedial strategies to be effective.     

In situ ground water denitrification in stratified, permeable soils underlying riparian wetlands

The ground water denitrification capacity of riparian zones in deep soils, where substantial ground water can flow through low-gradient stratified sediments, may affect watershed nitrogen export. We hypothesized that the vertical pattern of ground water denitrification in riparian hydric soils varies with geomorphic setting and follows expected subsurface carbon distribution (i.e., abrupt decline with depth in glacial outwash vs. negligible decline with depth in alluvium). We measured in situ ground water denitrification rates at three depths (65, 150, and 300 cm) within hydric soils at four riparian sites (two per setting) using a 15N-enriched nitrate "push-pull" method. No significant difference was found in the pattern and magnitude of denitrification when grouping sites by setting. At three sites there was no significant difference in denitrification among depths. Correlations of site characteristics with denitrification varied with depth. At 65 cm, ground water denitrification correlated with variables associated with the surface ecosystem (temperature, dissolved organic carbon). At deeper depths, rates were significantly higher closer to the stream where the subsoil often contains organically enriched deposits that indicate fluvial geomorphic processes. Mean rates ranged from 30 to 120 microg N kg(-1) d(-1) within 10 m versus <1 to 40 microg N kg(-1) d(-1) at >30 m from the stream. High denitrification rates observed in hydric soils, down to 3 m within 10 m of the stream in both alluvial and glacial outwash settings, argue for the importance of both settings in evaluating the significance of riparian wetlands in catchment-scale N dynamics.     

Soil erosion and sediment sources in an Ohio watershed using beryllium-7, cesium-137, and lead-210

Soil cores and suspended sediments were collected within the Old Woman Creek, Ohio (OWC) watershed following a thunderstorm and analyzed for 7Be, 137Cs, and 210Pb activities to compare the effects of till vs. no-till management on soil erosion and sediment yield. The upper reaches of the watershed draining tilled agricultural fields were disproportionately responsible for the majority of the suspended sediment load compared with lower in the watershed (2.0-7.0 metric tons/km2 [Mg/km2] vs. 1.2-2.6 Mg/km2). About 6 to 10 times more sediment was derived from the subbasins that are predominantly tilled (6.8-12.4 Mg/km2) compared with the subbasins undergoing no-till practices (0.5-1.1 Mg/km2). In undisturbed soils the 210Pb activities decreased with movement toward the bottom of the cores to the constant supported 210Pb value at a depth of about 10 cm. There was a subsurface maximum in 137Cs activity within the top 10 cm. In contrast, the 210Pb and 137Cs distributions in soils that are currently or were previously tilled were nearly homogeneous with depth, reflecting continuing or previous mixing by plowing. The activities of 210Pb and 7Be were linearly correlated and were higher in suspended sediments derived from no-till subbasins than those derived from tilled subbasins, indicating that the soil surface is the source of suspended sediment. This study demonstrates that no-till farming results in decreases in soil erosion and decreases in suspended sediment discharges and that those eroded sediments have a radionuclide signature corresponding to the tillage practice and the depth of erosion.     

The effect of river pulsing on sedimentation and nutrients in created riparian wetlands

Sedimentation under pulsed and steady-flow conditions was investigated in two created flow-through riparian wetlands in central Ohio over 2 yr. Hydrologic pulses of river water lasting for 6 to 8 d were imposed on each wetland from January through June during 2004. Mean inflow rates during pulses averaged 52 and 7 cm d(-1) between pulses. In 2005, the wetlands received a steady-flow regime of 11 cm d(-1) with no major hydrologic fluctuations. Thirty-two sediment traps were deployed and sampled once per month in April, May, June, and July for two consecutive years in each wetland. January through March were not sampled in either year due to frozen water surfaces in the wetlands. Gross sedimentation (sedimentation without normalizing for differences between years) was significantly greater in the pulsing study period (90 kg m(-2)) than in the steady-flow study period (64 kg m(-2)). When normalized for different hydrologic and total suspended solid inputs between years, sedimentation for April through July was not significantly different between pulsing and steady-flow study periods. Sedimentation for the 3 mo that received hydrologic pulses (April, May, and June) was significantly lower during pulsing months than in the corresponding steady-flow months. Large fractions of inorganic matter in collected sediments indicated that allochthonous inputs were the main contributor to sedimentation in these wetlands. Organic matter fractions of collected sediments were consistently greater in the steady-flow study period (1.8 g kg(-1)) than in the pulsed study period (1.5 g kg(-1)), consistent with greater primary productivity in the water column during steady-flow conditions.     

Selenium distribution and fluxes in intertidal wetlands, San Francisco Bay, California

Selenium (Se) concentrations exceeding ecological guidelines for sediments and suspended particulate matter (SPM) have been observed in the northern reach of the San Francisco Bay estuary. Longterm availability of elevated Se in wetland sediments depends in part on the fluxes controlling Se distribution. The relative contribution of sedimentary vs. post-depositional Se fluxes in two San Francisco Bay intertidal wetlands was estimated. Selenium concentrations on surface wetland sediments were compared with levels on SPM, and with previously established background levels in San Francisco Bay sediments. Sediment Se fluxes to the wetlands were measured directly using sediment traps. Although dissolved Se concentrations are higher than particulate Se concentrations in San Francisco Bay water, sediment input into the system provides the major flux of Se. Strong correlation between Se and C on SPM (r2 = 0.81) indicates the importance of organic particulate deposition. Dependence on sediment texture was qualitatively established by measuring Se on particle-size separates. Normalization to Al showed that 65% of Se spatial variability is related to sediment texture. Selenium is further enriched in the marsh via post-depositional inputs, probably due to in situ adsorption from overlying water and chemical reduction. According to sediment flux measurements, enrichment in the marsh is equivalent to 20 to 25% of the particulate Se flux, thereby defining the marsh as a Se sink. These findings highlight the need for more intensive monitoring of SPM as the major source of Se to intertidal wetlands.     

NITRATE TRANSFORMATIONS IN SOUTHERN ONTARIO STREAM SEDIMENTS1

The transformation of nitrate was investigated in diverse stream sediments from six areas of Southern Ontario, Canada. Laboratory Experiments conducted with intact 0-5 cm depth sediment cores overlain with aerated 5 mg/l nitrate-N solution reveald considerable nitrate depletion during a six-day period as a resuit of denitrification and nitrate reduction to ammonium. Nitrification and ammonification also occurred simultaneously with nitrate reduction in many stream sediments. Mixed 0-5 cm depth sediments collected from 81 stream sites were used to examine the relationship between microbial nitrate removal and sediment characteristics. Rates of nitrate-N loss from aerated 5 mg/l nitrate-N solutions overlying these sediments ranged between 11 and 171 mg/m²/day for a 24-hour incubation period. Rates of nitrate loss for the 24-hour period exhibited a significant positive correlation (r=0.72) with sediment ammonium content. Organic carbon, total nitrogen and sediment texture also had significant but weak correlations with nitrate loss.     

Using Fly Ash as a Marker to Quantify Culturally‐Accelerated Sediment Accumulation in Playa Wetlands

Wetlands in the Rainwater Basin in Nebraska are vulnerable to sediment accumulation from the surrounding watershed. Sediment accumulation has a negative impact on wetland quality by decreasing the depth and volume of water stored, and the plant community species composition and density growing in the wetland. The objective of this study was to determine the amount of sediment that has accumulated in five selected wetlands in the Rainwater Basin in Nebraska. Soil cores were taken at five or six locations along transects across each wetland. This study used the fly ash, which is generated by coal‐burning locomotives that were present generally in the late 1800s and early 1900s, as a marker to quantify the sediment deposition rates. The cores were divided into 5 cm sections and the soils were analyzed using a fly ash extraction and identification technique. Results indicate that the average depth of sediment ranged from 23.00 to 38.00 cm. The annual average depth of sediment accumulation ranged from 0.18 cm/yr to 0.29 cm/yr. The annual sediment accumulation rate from both wind erosion and water erosion in these five sampling wetlands was between 1.946 and 3.225 kg/m²/yr. The results of this research can be used to develop restoration plans for wetlands. The fly ash testing technology can also be applied to other areas with the railroads across the United States.     

Impact of Dredging on Phosphorus Transport in Agricultural Drainage Ditches of the Atlantic Coastal Plain1

Abstract: Drainage ditches can be a key conduit of phosphorus (P) between agricultural soils of the Atlantic Coastal Plain and local surface waters, including the Chesapeake Bay. This study sought to quantify the effect of a common ditch management practice, sediment dredging, on fate of P in drainage ditches. Sediments from two drainage ditches that had been monitored for seven years and had similar characteristics (flow, P loadings, sediment properties) were sampled (0‐5 cm) after one of the ditches had been dredged, which removed fine textured sediments (clay = 41%) with high organic matter content (85 g/kg) and exposed coarse textured sediments (clay = 15%) with low organic matter content (2.2 g/kg). Sediments were subjected to a three‐phase experiment (equilibrium, uptake, and release) in recirculating 10‐m‐long, 0.2‐m‐wide, and 5‐cm‐deep flumes to evaluate their role as sources and sinks of P. Under conditions of low initial P concentrations in flume water, sediments from the dredged ditch released 13 times less P to the water than did sediments from the ditch that had not been dredged, equivalent to 24 mg dissolved P. However, the sediments from the dredged ditch removed 19% less P (76 mg) from the flume water when it was spiked with dissolved P to approximate long‐term runoff concentrations. Irradiation of sediments to destroy microorganisms revealed that biological processes accounted for up to 30% of P uptake in the coarse textured sediments of the dredged ditch and 18% in the fine textured sediments of the undredged ditch. Results indicate that dredging of coastal plain drainage ditches can potentially impact the P buffering capacity of ditches draining agricultural soils with a high potential for P runoff.     

Dissolved phosphorus retention and release from a coastal plain in-stream wetland

Dissolved phosphorus (DP) can be released from wetlands as a result of flooding or shifts in water column concentrations. Our objectives were to determine the long-term (1460 d) DP retention and release characteristics of an in-stream wetland, and to evaluate how these characteristics respond to flooding, draining, and changes in DP concentrations. The studied in-stream wetland drains an agriculturally intensive subwatershed in the North Carolina Coastal Plain region. The wetland's DP retention and release characteristics were evaluated by measuring inflow and outflow DP concentrations, DP mass balance, and DP movement across the sediment-water column interface. Phosphorus sorption isotherms were measured to determine the sediment's equilibria P concentration (EPCo), and passive samplers were used to measure sediment pore water DP concentrations. Initially, the in-stream wetland was undersized (0.31 ha) and released 1.5 kg of DP. Increasing the in-stream wetland area to 0.67 ha by flooding resulted in more DP retention (28 kg) and low outflow DP concentrations. Draining the in-stream wetland from 0.67 to 0.33 ha caused the release of stored DP (12.1 kg). Shifts both in sediment pore water DP concentrations and sediment EPCo values corroborate the release of stored DP. Reflooding the wetland from 0.33 to 0.85 ha caused additional release of stored DP into the outflowing stream (10.9 kg). We conclude that for a time period, this in-stream wetland did provide DP retention. During other time periods, DP was released due to changes in wetland area, rainfall, and DP concentrations.     

Evaluation of phosphorus transport in surface runoff from packed soil boxes

Evaluation of phosphorus (P) management strategies to protect water quality has largely relied on research using simulated rainfall to generate runoff from either field plots or shallow boxes packed with soil. Runoff from unmanured, grassed field plots (1 m wide x 2 m long, 3-8% slope) and bare soil boxes (0.2 m wide and 1 m long, 3% slope) was compared using rainfall simulation (75 mm h(-1)) standardized by 30-min runoff duration (rainfall averaged 55 mm for field plots and 41 mm for packed boxes). Packed boxes had lower infiltration (1.2 cm) and greater runoff (2.9 cm) and erosion (542 kg ha(-1)) than field plots (3.7 cm infiltration; 1.8 cm runoff; 149 kg ha(-1) erosion), yielding greater total phosphorus (TP) losses in runoff. Despite these differences, regressions of dissolved reactive phosphorus (DRP) in runoff and Mehlich-3 soil P were consistent between field plots and packed boxes reflecting similar buffering by soils and sediments. A second experiment compared manured boxes of 5- and 25-cm depths to determine if variable hydrology based on box depth influenced P transport. Runoff properties did not differ significantly between box depths before or after broadcasting dairy, poultry, or swine manure (100 kg TP ha(-1)). Water-extractable phosphorus (WEP) from manures dominated runoff P, and translocation of manure P into soil was consistent between box types. This study reveals the practical, but limited, comparability of field plot and soil box data, highlighting soil and sediment buffering in unamended soils and manure WEP in amended soils as dominant controls of DRP transport.     

Particulate phosphorus transport within stream flow of an agricultural catchment

There is interest in quantifying phosphorus (P) loss from intensively grazed dairy landscapes to identify key pathways and target remediation methods. The Bog Burn drains a dairying catchment in Southland, New Zealand, and has been monitored at fortnightly intervals over a 12-mo period at four sites for suspended sediment (SS), dissolved reactive phosphorus (DRP), and total phosphorus (TP). Time-integrated samplers, deployed at 0.6 median water depth at each site (calculated from previous year's flow data), collected sediment samples, which were analyzed for SS, bioavailable phosphorus (BAP), and TP. Mean concentrations of DRP and TP in stream flow and BAP and TP in sediment were generally highest in summer or autumn (0.043 mg DRP L(-1), 0.160 mg TP L(-1), 173 mg BAP kg(-1), 2228 mg TP kg(-1)) and lowest in winter or spring (0.012 mg DRP L(-1), 0.034 mg TP L(-1), 6 mg BAP kg(-1), 711 mg TP kg(-1)), while loads were highest in winter. Analysis of (137)Cs concentrations in trapped sediment, topsoil, subsoil, and stream bed and bank sediment indicated that trapped sediment was derived from topsoil and entered the stream either through tile drainage or, to a lesser extent, overland flow. Because concentrations of DRP and TP in stream flow are in excess of recommended limits for good water quality (>0.01 mg DRP L(-1), 0.033 mg TP L(-1)), management should focus on the topsoil and specifically on decreasing P loss via tile drainage. This is best achieved by decreasing soil Olsen P concentrations, especially because, on average, Olsen P concentrations in the catchment were above the agronomic optimum.