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.     

Two‐Stage Ditch Floodplains Enhance N‐Removal Capacity and Reduce Turbidity and Dissolved P in Agricultural Streams

Two‐stage ditches represent an emerging management strategy in artificially drained agricultural landscapes that mimics natural floodplains and has the potential to improve water quality. We assessed the potential for the two‐stage ditch to reduce sediment and nutrient export by measuring water column turbidity, nitrate (NO₃^?), ammonium (NH₄⁺), and soluble reactive phosphorus (SRP) concentrations, and denitrification rates. During 2009‐2010, we compared reaches with two‐stage floodplains to upstream reaches with conventional trapezoid design in six agricultural streams. At base flow, these short two‐stage reaches (<600 m) reduced SRP concentrations by 3‐53%, but did not significantly reduce NO₃^? concentrations due to very high NO₃^? loads. The two‐stage also decreased turbidity by 15‐82%, suggesting reduced suspended sediment export during floodplain inundation. Reach‐scale N‐removal increased 3‐24 fold during inundation due to increased bioreactive surface area with high floodplain denitrification rates. Inundation frequency varied with bench height, with lower benches being flooded more frequently, resulting in higher annual N‐removal. We also found both soil organic matter and denitrification rates were higher on older floodplains. Finally, influence of the two‐stage varied among streams and years due to variation in stream discharge, nutrient loads, and denitrification rates, which should be considered during implementation to optimize potential water quality benefits.     

FATE OF NITROGEN AND PHOSPHORUS ENTERING A GULF COAST FRESHWATER LAKE: A CASE STUDY1

ABSTRACT: Nitrogen and P fluxes, transformations and water quality functions of Lake Verret (a coastal Louisiana freshwater lake), were quantified. Ortho-P, total-P, NH₄⁺-N NO₃ -N and TKN in surface water collected from streams feeding Lake Verret averaged 104, 340, 59, 185, and 1,060 mg 1^?1, respectively. Lake Verret surface water concentrations of ortho-P, total-P, NH⁺-N, NO₃^?_-N and TKN averaged 66, 191, 36, 66, and 1,292 μg 1^?1. The higher N and P concentrations were located in areas of the lake receiving drainage. Nitrification and denitrification processes were significant in removing appreciable inorganic N from the system. In situ denitrification rates determined from acetylene inhibition techniques show the lake removes 560 mg N m^?2 yr^?1. Laboratory investigations using sediment receiving 450 μg NH⁺₄-N (N-15 labeled) showed that the lake has the potential to remove up to 12.8 g N m^?2 yr^?1. Equilibrium studies of P exchanges between the sediment and water column established the potential or adsorption capacity of bottom sediment in removing P from the overlying water. Lake Verret sediment was found to adsorb P from the water column at concentrations above 50 μg P 1^?1 and the adsorption rates were as great as 300 μg P cm^?2 day^?1 Using the ¹³⁷C s dating techniques, approximately 18 g N m^?2 yr^?1 and 1.2 g P m^?2 yr^?1 were removed from the system via sedimentation. Presently elevated nutrient levels are found only in the upper reaches of the lake receiving nutrient input from runoff from streams draining adjacent agricultural areas. Nitrification, denitrification, and adsorption processes at the sediment water interface over a relatively short distance reduces the N and P levels in the water column. However, if the lake receives additional nutrient loading, elevated levels will likely cover a larger portion of the lake, further reducing water quality in the lake.     

DIN Retention‐Transport Through Four Hydrologically Connected Zones in a Headwater Catchment of the Upper Mississippi River1

Abstract: Dissolved inorganic nitrogen (DIN) retention‐transport through a headwater catchment was synthesized from studies encompassing four distinct hydrologic zones of the Shingobee River Headwaters near the origin of the Mississippi River. The hydrologic zones included: (1) hillslope ground water (ridge to bankside riparian); (2) alluvial riparian ground water; (3) ground water discharged through subchannel sediments (hyporheic zone); and (4) channel surface water. During subsurface hillslope transport through Zone 1, DIN, primarily nitrate, decreased from ～3 mg‐N/l to <0.1 mg‐N/l. Ambient seasonal nitrate:chloride ratios in hillslope flow paths indicated both dilution and biotic processing caused nitrate loss. Biologically available organic carbon controlled biotic nitrate retention during hillslope transport. In the alluvial riparian zone (Zone 2) biologically available organic carbon controlled nitrate depletion although processing of both ambient and amended nitrate was faster during the summer than winter. In the hyporheic zone (Zone 3) and stream surface water (Zone 4) DIN retention was primarily controlled by temperature. Perfusion core studies using hyporheic sediment indicated sufficient organic carbon in bed sediments to retain ground water DIN via coupled nitrification‐denitrification. Numerical simulations of seasonal hyporheic sediment nitrification‐denitrification rates from perfusion cores adequately predicted surface water ammonium but not nitrate when compared to 5 years of monthly field data (1989‐93). Mass balance studies in stream surface water indicated proportionally higher summer than winter N retention. Watershed DIN retention was effective during summer under the current land use of intermittently grazed pasture. However, more intensive land use such as row crop agriculture would decrease nitrate retention efficiency and increase loads to surface water. Understanding DIN retention capacity throughout the system, including special channel features such as sloughs, wetlands and floodplains that provide surface water‐ground water connectivity, will be required to develop effective nitrate management strategies.     

Bioremediation of residual fertilizer nitrate: II. Soil redox potential and soluble iron as indicators of soil health during treatment

The prospect of using wastewater containing high loads of soluble organic matter (OM) for removing residual agricultural chemicals (fertilizer, pesticide, or herbicide) in farm soil, although promising, could have adverse effects on soil agricultural quality as a result of development of redoximorphic features in the soil profile. In this study, the effect of organic carbon supplement for bioremediation of residual fertilizer nitrate on soil properties, redox potential (Eh), pH, and metal ion mobilization was studied using sandy soils packed in columns. The study was included in a general project, described elsewhere (Ugwuegbu et al., 2000), undertaken to evaluate use of controlled water table management (WTM) systems to supply organic carbon for creating a reduced environment conducive to denitrification of residual fertilizer nitrate leaching from the farm to subsurface water. The columns were subjected to subirrigation with water containing soluble organic carbon in the form of glucose. The work was carried out in two experimental setups and the long-term effect of a range of glucose concentrations on the Eh, pH, and soluble levels of Fe and Mn was investigated. From the results obtained, it could be concluded that excessive organic carbon supplement to soil can have adverse effects on soil quality and that Eh and soluble Fe are the two most practical parameters for monitoring soil health during treatment of farm chemicals.     

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.     

Estimating Nitrogen Loading to Ground Water and Assessing Vulnerability to Nitrate Contamination in a Large Karstic Springs Basin,Florida1

Abstract: A nitrogen (N) mass‐balance budget was developed to assess the sources of N affecting increasing ground‐water nitrate concentrations in the 960‐km² karstic Ichetucknee Springs basin. This budget included direct measurements of N species in rainfall, ground water, and spring waters, along with estimates of N loading from fertilizers, septic tanks, animal wastes, and the land application of treated municipal wastewater and residual solids. Based on a range of N leaching estimates, N loads to ground water ranged from 262,000 to 1.3 million kg/year; and were similar to N export from the basin in spring waters (266,000 kg/year) when 80‐90% N losses were assumed. Fertilizers applied to cropland, lawns, and pine stands contributed about 51% of the estimated total annual N load to ground water in the basin. Other sources contributed the following percentages of total N load to ground water: animal wastes, 27%; septic tanks, 12%; atmospheric deposition, 8%; and the land application of treated wastewater and biosolids, 2%. Due to below normal rainfall (97.3 cm) during the 12‐month rainfall collection period, N inputs from rainfall likely were about 30% lower than estimates for normal annual rainfall (136 cm). Low N‐isotope values for six spring waters (δ¹⁵N‐NO₃ = 3.3 to 6.3‰) and elevated potassium concentrations in ground water and spring waters were consistent with the large N contribution from fertilizers. Given ground‐water residence times on the order of decades for spring waters, possible sinks for excess N inputs to the basin include N storage in the unsaturated zone and parts of the aquifer with relatively sluggish ground‐water movement and denitrification. A geographical‐based model of spatial loading from fertilizers indicated that areas most vulnerable to nitrate contamination were located in closed depressions containing sinkholes and other dissolution features in the southern half of the basin.     

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.     

CARBON CONTENT OF SEDIMENTS OF SMALL RESERVOIRS1

ABSTRACT: Carbon content was measured in sediments deposited in 58 small reservoirs across the United States. Reservoirs varied from 0.2 to 4000 km2 in surface area. The carbon content of sediment ranged from 0.3 to 5.6 percent, with a mean of 1.9 ± 1.1 percent. No significant differences between the soil and sediment carbon content were found using a paired t-test or ANOVA. The carbon content of sediments in reservoirs was similar to the carbon content of surface soils (0–10 cm) in the watershed, except in watersheds with shrub or steppe (desert) vegetation. Based on the sediment accumulation rates measured in each reservoir, the calculated organic carbon accumulation rates among reservoirs ranged from 26 to 3700 gC m^-2yr^-1, with a mean of 675 ± 739 gC m^-2yr^-1. The carbon content and accumulation rates were highest in sediments from grassland watersheds. High variability was found in carbon content, carbon accumulation, and sediment accumulation rates due to individual watershed and reservoir characteristics rather than to any broad physiographic patterns. The carbon accumulation rates in these reservoir sediments indicate that reservoir sediments could be a significant sink for organic carbon.     

Identification of Sediment Sources in Forested Watersheds With Surface Coal Mining Disturbance Using Carbon and Nitrogen Isotopes1

Abstract: Sediments and soils were analyzed using stable carbon and nitrogen isotope ratio mass spectrometry and carbon and nitrogen elemental analyses to evaluate the their ability to indicate land‐use and land management disturbance and pinpoint loading from sediment transport sources in forested watersheds disturbed by surface coal mining. Samples of transported sediment particulate organic matter were collected from four watersheds in the Southern Appalachian forest region of southeastern Kentucky. The four watersheds had different surface coal mining history that were classified as undisturbed, active mining, and reclaimed conditions. Soil samples were analyzed including reclaimed grassland soils, undisturbed forest soils, geogenic organic matter associated with coal fragments in mining spoil, and soil organic matter from un‐mined grassland soils. Statistically significant differences were found for all biogeochemical signatures when comparing transported sediments from undisturbed watersheds and surface coal mining disturbed watersheds, and the results were attributed to differences in erosion sources and the presence of geogenic organic matter. Sediment transport sources in the surface coal mining watersheds were analyzed using Monte Carlo mass balance un‐mixing and it was found that: δ¹⁵N showed the ability to differentiate streambank erosion and surface soil erosion; and δ¹³C showed the ability to differentiate soil organic matter and geogenic organic matter. Results from the analyses suggest that streambank erosion downstream of surface coal mining sites is an especially significant source of sediment in coal mining disturbed watersheds. Further, the results suggest that the sediment transport processes governing streambank erosion loads are taking longer to reach geomorphologic equilibrium in the watershed as compared with the surface erosion processes. The dual‐isotope technique provides a useful method for further investigation of the impact of surface coal mining in the uplands of the watershed upon the geomorphologic state of the channel and the source of organic matter in aquatic systems impacted by surface coal mining.     

Simulation of Nitrogen Transport in Soil Under Municipal Wastewater Application Using LEACHN1

Abstract: To reduce the risk of surface and ground water pollution from nitrate, and in so doing improve the quality of receiving waters, better management options for land application of wastewater must be explored. In order to determine proper and environmentally safe wastewater land application methods, different application scenarios were simulated in this study to determine the fate and transport of nitrogen in sand‐filled field lysimeters. The Leaching Estimation and CHemistry Model for Nutrients (LEACHN) model was used to assess alternative wastewater land application scenarios: applications of low‐, medium‐, or high‐N concentration wastewaters, at different rates (0.06, 0.19, 0.31, or 0.6 m³/m²/day), under continuous or intermittent application. In the simulations, the NO₃^?‐N levels decreased in the leachate with an increase in wastewater application rates, due to enhanced denitrification in the upper anoxic zone of the soil generated under high flow rates. With low‐N concentrated wastewater, under all tested flow rates, the NO₃^?‐N levels in the leachate were below the permissible limit. When medium‐N wastewater was applied, the NO₃^?‐N level in leachate from the highest flow rate was below the permissible limit. Therefore, wastewater with low‐N concentrations, about 10 and 0.5 mg/l NO₃^?‐N and NH₄⁺‐N, may be continuously applied to soil at all tested flow rates, with minimal nitrate pollution problems. Medium and high‐N concentrated wastewaters increased nitrate levels in the leachate, as compared to their levels in the low‐N concentrated wastewater. It appears that while low‐N wastewater can be safely applied to land without much nitrate leaching problems, the application of medium and high‐N wastewater could pose nitrate pollution problems. The simulation with intermittent application of low‐, medium‐, and high‐N concentrated wastewater at different rates showed a 51‐89% greater reduction in NO₃^?‐N levels in the leachate, than for continuous application under all tested wastewater N‐levels and flow rates. Also, the levels of NO₃^?‐N in their leachates were below the permissible limit. Therefore, wastewater with high levels of nitrogenous compounds (up to 54 NO₃‐N mg/l) could be treated through an intermittent application to land.     

NITROGEN TRANSFORMATIONS IN SEDIMENTS AS AFFECTED BY CHEMICAL AMENDMENTS1

ABSTRACT: A study was conducted to elucidate some of the chemical factors affecting the rate and pathways of N transformations in lake sediments. The main emphasis was placed on modifying a noncalcareous sediment with CaCO₃ to approximate the composition of a calcareous sediment. Additionally, the effects of Ca²⁺, CO₃^2-, Mg2⁺ and OH^- were evaluated by using appropriate chemicals. Further, the effect of aluminum sulfate was evaluated with both sediment types. Sediment pH at 7 days was not affected by CaCO₃, but was decreased by aluminum sulfate. The CaCO₃ treatment increased the rate of ammonification, nitrification, reduction of acetylene to ethylene and methane formation, while with few exceptions the other treatments decreased the rate of the transformations studied. Aluminum sulfate, which has been proposed as a lake restoration treatment, increased ammonification but decreased most of the other transformations.     

Hydrologic Controls on Nitrogen and Phosphorous Dynamics in Relict Oxbow Wetlands Adjacent to an Urban Restored Stream

Although wetlands are known to be sinks for nitrogen (N) and phosphorus (P), their function in urban watersheds remains unclear. We analyzed water and nitrate (NO₃^?) and phosphate (PO₄^3?) dynamics during precipitation events in two oxbow wetlands that were created during geomorphic stream restoration in Baltimore County, Maryland that varied in the nature and extent of connectivity to the adjacent stream. Oxbow 1 (Ox1) received 1.6‐4.2% and Oxbow 2 (Ox2) received 4.2‐7.4% of cumulative streamflow during storm events from subsurface seepage (Ox1) and surface flow (Ox2). The retention time of incoming stormwater ranged from 0.2 to 6.7 days in Ox1 and 1.8 to 4.3 days in Ox2. Retention rates in the wetlands ranged from 0.25 to 2.74 g N/m²/day in Ox1 and 0.29 to 1.94 g N/m²/day in Ox2. Percent retention of the NO₃^?‐N load that entered the wetlands during the storm events ranged from 64 to 87% and 23 to 26%, in Ox1 and Ox2, respectively. During all four storm events, Ox1 and Ox2 were a small net source of dissolved PO₄^3? to the adjacent stream (i.e., more P exited than entered the wetland), releasing P at a rate of 0.23‐20.83 mg P/m²/day and 3.43‐24.84 mg P/m²/day, respectively. N and P removal efficiency of the oxbows were regulated by hydrologic connectivity, hydraulic loading, and retention time. Incidental oxbow wetlands have potential to receive urban stream and storm flow and to be significant N sinks, but they may be sources of P in urban watersheds.     

EFFECTS OF FOREST FERTILIZATION ON STREAM WATER CHEMISTRY IN THE APPALACHIANS1

ABSTRACT: Stream water chemistry was monitored on two watersheds on the Fernow Experimental Forest in north-central West Virginia to determine the effects of forest fertilization on annual nutrient exports. Ammonium nitrate and triple superphosphate were applied simultaneously at rates of 336 kg ha^?1 N and 224 kg ha^?1 P₂O₅, respectively, which are similar to rates used in commercial forest operations. The treatment significantly increased outputs of several ions. Annual outputs of nitrate N increased as much as 18 times over pretreatment levels, and calcium and magnesium increased as much as three times over pretreatment levels the first year after fertilization. Outputs for these nutrients were elevated for all three post-treatment years. Although nitrate N increased significantly, only about 20 percent of the applied fertilizer was accounted for in stream water exports. Outputs of phosphate P declined following fertilization, probably because the watersheds are phosphorus deficient, but by the third year, they slightly exceeded predicted values. Estimated nutrient losses to deep seepage were substantial, especially on the leakier south-facing catchmeat, on which some nutrient losses were equal to or greater than those in stream water. When the nutrient exports associated with both stream discharge and ground water recharge were combined, the percentages of applied N that were lost were similar on the two watersheds, averaging 27.5 percent. Less than 1 percent of the applied P was lost from either watershed in the combination of streamflow and deep seepage.     

Instream Large Wood: Denitrification Hotspots with Low N2O Production

We examined the effect of instream large wood on denitrification capacity in two contrasting, lower order streams — one that drains an agricultural watershed with no riparian forest and minimal stores of instream large wood and another that drains a forested watershed with an extensive riparian forest and abundant instream large wood. We incubated two types of wood substrates (fresh wood blocks and extant streambed wood) and an artificial stone substrate for nine weeks in each stream. After in situ incubation, we collected the substrates and their attached biofilms and established laboratory‐based mesocosm assays with stream water amended with ¹⁵N‐labeled nitrate‐N. Wood substrates at the forested site had significantly higher denitrification than wood substrates from the agricultural site and artificial stone substrates from either site. Nitrate‐N removal rates were markedly higher on woody substrates compared to artificial stones at both sites. Nitrate‐N removal rates were significantly correlated with biofilm biomass. Denitrification capacity accounted for only a portion of nitrate‐N removal observed within the mesocosms in both the wood controls and instream substrates. N₂ accounted for 99.7% of total denitrification. Restoration practices that generate large wood in streams should be encouraged for N removal and do not appear to generate high risks of instream N₂O generation.     

Nitrate Dynamics in Two Streams Impacted by Wastewater Treatment Plant Discharge: Point Sources or Sinks?

We examined nitrate processing in headwater stream reaches downstream of two wastewater treatment plant outfalls during low streamflow. Our objectives were to quantify nitrate mass flux before and after effluent discharge and to use field and laboratory techniques to assess the mechanism of nitrate uptake. Microcosm experiments were utilized to determine the location of nitrate processing, and molecular biomarkers were used to detect and quantify microbial denitrification. At one site, downstream nitrate mass flux was significantly (p = 0.01) lower than sum of upstream and wastewater effluent fluxes, indicating rapid stream assimilation of incoming nitrate in the vicinity of the point source. Microcosm experiments supported the theory that nitrate processing occurs in sediments. Molecular assays for denitrifcation‐associated functional genes nosZ, nirS, and nirK, provided evidence that effluent contained enriched denitrifying communities relative to ambient stream water. Nitrate loss at the site with greater uptake was correlated with sulfate loss (p < 0.01; r² = 0.86), suggesting a possible link between sulfate reducing bacteria and denitrifying bacterial communities. Results suggest there is an opportunity to better understand nitrate dynamics in cases where point sources may act as point sinks under specific sets of conditions.     

EFFECT OF A POINT SOURCE INPUT ON STREAM NUTRIENT RETENTION1

ABSTRACT: We examined the effect of a point source (PS) input on water chemistry and nutrient retention in Spavinaw Creek, Arkansas, during summer baseflows in 1998 and 1999. The nutrient uptake length (S_w) concept was used to quantify the impact of nutrient inputs in the receiving stream. We used an artificial injection upstream of the PS inputs to estimate background S and used the natural decline in nutrient concentrations below the PS to estimate the net nutrient uptake length (S_net). S_w for soluble reactive phosphorus (SRP) in the upstream reference section was O.75 km, but S_net ranged from 9.0 to 31 km for SRP and 3.1 to 12 km for NO₃‐N in the reach below the PS. S_net‐SRP was significantly correlated with discharge whereas S_net‐NO₃‐N was correlated with the amount of NO₃‐N enrichment from the PS. In order to examine specific mechanisms of P retention, loosely exchangeable P and P Sorption Index (PSI) of stream sediments were measured. Sediments exhibited little natural P buffering capacity (low PSI) above the PS, but P loading from the PS further reduced PSI. Loosely exchangeable P in the sediments also increased three fold below the PS, indicating sediments removed some water column P. The physical process of flow and sediment sorption apparently regulated P retention in Spavinaw Creek, whereas the level of N enrichment and possibly biotic uptake and denitrification influenced N retention. Regardless of the mechanism, Spavinaw Creek demonstrated little ability to retain PS‐added nutrients because net nutrient uptake lengths were in the km range.     

Persistent elevated nitrate in a riparian zone aquifer

Streamside vegetated buffer strips (riparian zones) are often assumed to be zones of ground water nitrate (NO3(-)) attenuation. At a site in southwestern Ontario (Zorra site), detailed monitoring revealed that elevated NO3(-) -N (4-93 mg L(-1)) persisted throughout a 100-m-wide riparian floodplain. Typical of riparian zones, the site has a soil zone of recent river alluvium that is organic carbon (OC) rich (36 +/- 16 g kg(-1)). This material is underlain by an older glacial outwash aquifer with a much lower OC content (2.3 +/- 2.5 g kg(-1). Examination of NO3(-), Cl(-), SO4(2-), and dissolved organic carbon (DOC) concentrations; N/Cl ratios; and NO3(-) isotopic composition (delta15N and delta18O) provides evidence of four distinct NO3(-) source zones within the riparian environment. Denitrification occurs but is incomplete and is restricted to a narrow interval located within ~0.5 m of the alluvium-aquifer contact and to one zone (poultry manure compost zone) where elevated DOC persists from the source. In older ground water close to the river discharge point, denitrification remains insufficient to substantially deplete NO3(-). Overall, denitrification related specifically to the riparian environment is limited at this site. The persistence of NO3(-) in the aquifer at this site is a consequence of its Pleistocene age and resulting low OC content, in contrast to recent fluvial sediments in modern agricultural terrain, which, even if permeable, usually have zones enriched in labile OC. Thus, sediment age and origin are additional factors that should be considered when assessing the potential for riparian zone denitrification.     

SEDIMENT,NITRATE, AND AMMONIUM IN SURFACE RUNOFF FROM TWO TAHOE BASIN SOIL TYPES 1

ABSTRACT: Few studies have addressed the natural pollution potential of pristine subalpine forested watersheds on a site-specific basis. Consequently, specific source and amounts of nutrient discharge to tributaries of the Tahoe Basin are difficult to identify. The sediment content and nitrate and ammonium levels in surface runoff from two soil types (Meeks and Umpa), four plot conditions (wooded natural and disturbed, open natural and disturbed), and three slopes (gentle, moderate, and steep) were studied using rainfall simulation that applied a 9 cm h¹, 1-h event. A significant (P ≤ 0.005) two-way interaction between soil type and plot condition affected runoff nitrate concentration. Runoff from natural or disturbed open plots contained significantly (P = 0.05) greater nitrate than wooded plots. Peak concentrations of nitrate commonly occurred during early runoff, suggesting that peak nitrate discharge to Lake Tahoe tributaries can be expected during early runoff from snowmelt and summer precipitation events. The highest nitrate runoff concentration and 1-h cumulative loading from the 0.46 m² plots were 6.7 mg L-¹ (Umpa, open natural, 15–30 percent slope), and 0.7 mg (Umpa, open natural, ≥ 30 percent slope), respectively. Ammonium in surface runoff was generally below detection limits (≤ 0.05 μg L^?1). No statistical relationship between runoff nitrate and sediment discharge was detected.     

Influence of geomorphological variability in channel characteristics on sediment denitrification in agricultural streams

Within fluvial systems, the spatial variability of geomorphological characteristics of stream channels and associated streambed properties can affect many biogeochemical processes. In agricultural streams of the midwestern USA, it is not known how geomorphological variability affects sediment denitrification rates, a potentially important loss mechanism for N. Sediment denitrification was measured at channelized and meandering headwater reaches in east-central Illinois, a region dominated by intensive agriculture and high NO(3)-N stream export, between June 2003 and February 2005 using the chloramphenicol-amended acetylene inhibition procedure. Sediment denitrification rates were greatest in separation zones, ranging from 0.6 to 76.4 mg N m(-2) h(-1), compared with riffles, point bars, pools, and a run ranging from 0 to 36.5 mg N m(-2) h(-1). Differences in benthic organic matter (r = 0.70) and the percentage of fine-grained sediments (r = 0.93) in the streambeds controlled much of the spatial variations in sediment denitrification among the geomorphological features. Although two meandering study reaches removed 390 and 99% more NO(3)-N by sediment denitrification than adjacent channelized reaches, NO(3)-N loss rates from all reaches were between 0.1 and 15.7% d(-1), except in late summer. Regardless of geomorphological characteristics, streams in east-central Illinois were not able to process the high NO(3)-N loads, making sediment denitrification in this region a limited sink for N.