Seasonal greenhouse gas emissions (methane, carbon dioxide, nitrous oxide) from engineered landfills: daily, intermediate, and final California cover soils

Compared with natural ecosystems and managed agricultural systems, engineered landfills represent a highly managed soil system for which there has been no systematic quantification of emissions from coexisting daily, intermediate, and final cover materials. We quantified the seasonal variability of CH, CO, and NO emissions from fresh refuse (no cover) and daily, intermediate, and final cover materials at northern and southern California landfill sites with engineered gas extraction systems. Fresh refuse fluxes (g m d [± SD]) averaged CH 0.053 (± 0.03), CO 135 (± 117), and NO 0.063 (± 0.059). Average CH emissions across all cover types and wet/dry seasons ranged over more than four orders of magnitude (<0.01-100 g m d) with most cover types, including both final covers, averaging <0.1 g m d with 10 to 40% of surface areas characterized by negative fluxes (uptake of atmospheric CH). The northern California intermediate cover (50 cm) had the highest CH fluxes. For both the intermediate (50-100 cm) and final (>200 cm) cover materials, below which methanogenesis was well established, the variability in gaseous fluxes was attributable to cover thickness, texture, density, and seasonally variable soil moisture and temperature at suboptimal conditions for CH oxidation. Thin daily covers (30 cm local soil) and fresh refuse generally had the highest CO and NO fluxes, indicating rapid onset of aerobic and semi-aerobic processes in recently buried refuse, with rates similar to soil ecosystems and windrow composting of organic waste. This study has emphasized the need for more systematic field quantification of seasonal emissions from multiple types of engineered covers.     

In vitro methane removal by volcanic pumice soil biofilter columns over one year

Soil methane (CH(4)) biofilters, containing CH(4)-oxidizing bacteria (methanotrophs), are a promising technology for mitigating greenhouse gas emissions. However, little is known about long-term biofilter performance. In this study, volcanic pumice topsoils (0-10 cm) and subsoils (10-50 cm) were tested for their ability to oxidize a range of CH(4) fluxes over 1 yr. The soils were sampled from an 8-yr-old and a 2-yr-old grassed landfill cover and from a nearby undisturbed pasture away from the influence of CH(4) generated by the decomposing refuse. Methane was passed through the soils in laboratory chambers with fluxes ranging from 0.5 g to 24 g CH(4) m(-3) h(-1). All topsoils efficiently oxidized CH(4). The undisturbed pasture topsoil exhibited the highest removal efficiency (24 g CH(4) m(-3) h(-1)), indicating rapid activation of the methanotroph population to the high CH(4) fluxes. The subsoils were less efficient at oxidizing CH(4) than the topsoils, achieving a maximum rate oxidation rate of 7 g CH(4) m(-3) h(-1). The topsoils exhibited higher porosities; moisture contents; surface areas; and total C, N, and available-P concentrations than the subsoils, suggesting that these characteristics strongly influence growth and activity of the CH(4)-oxidizing bacteria. Soil pH values and available-P levels gradually declined during the trial, indicating a need to monitor chemical parameters closely so that adjustments can be made when necessary. However, other key soil physicochemical parameters (moisture, total C, total N) increased over the course of the trial. This study showed that the selected topsoils were capable of continually sustaining high CH(4) removal rates over 1 yr, which is encouraging for the development of biofilters as a low-maintenance greenhouse gas mitigation technology.     

Evaluation of nitrate nitrogen fluxes from a tile-drained watershed in central Iowa

Nitrate N fluxes from tile-drained watersheds have been implicated in water quality studies of the Mississippi River basin, but actual NO3-N loads from small watersheds during long periods are poorly documented. We evaluated discharge and NO3-N fluxes passing the outlet of an Iowa watershed (5134 ha) and two of its tile-drained subbasins (493 and 863 ha) from mid-1992 through 2000. The cumulative NO3-N load from the catchment was 168 kg ha(-1), and 176 and 229 kg ha(-1) from the subbasins. The outlet had greater total discharge (1831 mm) and smaller flow-weighted mean NO3-N concentration (9.2 mg L(-1)) than the subbasins, while the larger subbasin had greater discharge (1712 vs. 1559 mm) and mean NO3-N concentration (13.4 vs. 11.3 mg L(-1)) than the smaller subbasin. Concentrations exceeding 10 mg L(-1) were common, but least frequent at the outlet. Nitrate N was generally not diluted by large flows, except during 1993 flooding. The outlet showed smaller NO3-N concentrations at low flows. Relationships between discharge and NO3-N flux showed log-log slopes near 1.0 for the subbasins, and 1.2 for the outlet, considering autocorrelation and measurement-error effects. We estimated denitrification of subbasin NO3-N fluxes in a hypothetical wetland using published data. Assuming that temperature and NO3-N supply could limit denitrification, then about 20% of the NO3-N would have been denitrified by a wetland constructed to meet USDA-approved criteria. The low efficiency results from the seasonal timing and NO3-N content of large flows. Therefore, agricultural and wetland best management practices (BMPs) are needed to achieve water quality goals in tile-drained watersheds.     

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.     

Effect of sampling frequency on estimates of cumulative nitrous oxide emissions

It is generally recognized that soil N(2)O emissions can exhibit pronounced day-to-day variations; however, measurements of soil N(2)O flux with soil chambers typically are done only at discrete points in time. This study evaluated the impact of sampling frequency on the precision of cumulative N(2)O flux estimates calculated from field measurements. Automated chambers were deployed in a corn/soybean field and used to measure soil N(2)O fluxes every 6 h from 25 Feb. 2006 through 11 Oct. 2006. The chambers were located in two positions relative to the fertilizer bands-directly over a band or between fertilizer bands. Sampling frequency effects on cumulative N(2)O-N flux estimation were assessed using a jackknife technique where populations of N(2)O fluxes were constructed from the average daily fluxes measured in each chamber. These test populations were generated by selecting measured flux values at regular time intervals ranging from 1 to 21 d. It was observed that as sampling interval increased from 7 to 21 d, variances associated with cumulative flux estimates increased. At relatively frequent sampling intensities (i.e., once every 3 d) N(2)O-N flux estimates were within +/-10% of the expected value at both sampling positions. As the time interval between sampling was increased, the deviation in estimated cumulative N(2)O flux increased, such that sampling once every 21 d yielded estimates within +60% and -40% of the actual cumulative N(2)O flux. The variance of potential fluxes associated with the between-band positions was less than the over-band position, indicating that the underlying temporal variability impacts the efficacy of a given sampling protocol.     

Nitrogen fluxes through unsaturated zones in five agricultural settings across the United States

The main physical and chemical controls on nitrogen (N) fluxes between the root zone and the water table were determined for agricultural sites in California, Indiana, Maryland, Nebraska, and Washington from 2004 to 2005. Sites included irrigated and nonirrigated fields; soil textures ranging from clay to sand; crops including corn, soybeans, almonds, and pasture; and unsaturated zone thicknesses ranging from 1 to 22 m. Chemical analyses of water from lysimeters and shallow wells indicate that advective transport of nitrate is the dominant process affecting the flux of N below the root zone. Vertical profiles of (i) nitrogen species, (ii) stable isotopes of nitrogen and oxygen, and (iii) oxygen, N, and argon in unsaturated zone air and correlations between N and other agricultural chemicals indicate that reactions do not greatly affect N concentrations between the root zone and the capillary fringe. As a result, physical factors, such as N application rate, water inputs, and evapotranspiration, control the differences in concentrations among the sites. Concentrations of N in shallow lysimeters exhibit seasonal variation, whereas concentrations in lysimeters deeper than a few meters are relatively stable. Based on concentration and recharge estimates, fluxes of N through the deep unsaturated zone range from 7 to 99 kg ha(-1) yr(-1). Vertical fluxes of N in ground water are lower due to spatial and historical changes in N inputs. High N fluxes are associated with coarse sediments and high N application rates.     

Lagoon-biogas emissions and carbon balance estimates of a swine production facility

Gaseous emissions from animal manure storage facilities can contribute to global greenhouse gas inventories. Biogas fluxes were measured for one year from a 2-ha anaerobic lagoon that received waste from a 10500-head swine (Sus scrofa) finishing operation in southwestern Kansas. During 2001, ebullition of biogas was measured continuously by using floating platforms equipped with gas-collection domes. Periodically, the composition of the biogas was determined by using gas chromatography. Detailed records of feed quality and quantity and animal weights and gains also were obtained to determine the carbon budget of the facility (barns and lagoon). Flux of biogas was very seasonal, with peak emission (18.7 mol m(-2) d(-1)) occurring in early June. Nearly 50% of the annual biogas losses occurred during a 30-d period beginning on day of year (DOY) 146. Flux patterns suggest that the start of the high biogas production period was governed by temperature, while the decline in production in mid-June was caused by substrate limitations. Average biogas composition was 0.71 L CH4 L(-1). The quantity of CH4 released from the lagoon was 86.3 Mg yr(-1), which represents about 38 g of CH4 per kg of animal weight gain. The average flux density of biogas from the lagoon was 382 mol m(-2) yr(-1) or 728 mol yr(-1) per resident animal where the resident animal population was 10500. Flux rates of CH4 were 1.7 to 3.4 times less than predictions made with Intergovernmental Panel on Climate Change (IPCC) models. Additional research is needed on the carbon budgets of other animal feeding operations so that better estimates of greenhouse gas emissions can be determined.     

POTENTIAL CLIMATE CHANGE IMPACTS ON WATER RESOURCES IN THE GREAT PLAINS1

ABSTRACT: This paper reports on the current assessment of climate impacts on water resources, including aquatic ecosystems, agricultural demands, and water management, in the U.S. Great Plains. Climate change in the region may have profound effects on agricultural users, aquatic ecosystems, and urban and industrial users alike. In the central Great Plains Region, the potential impacts of climate changes include changes in winter snowfall and snow-melt, growing season rainfall amounts and intensities, minimum winter temperature, and summer time average temperature. Specifically, results from general circulation models indicate that both annual average temperatures and total annual precipitation will increase over the region. However, the seasonal patterns are not uniform. The combined effect of these changes in weather patterns and average seasonal climate will affect numerous sectors critical to the economic, social and ecological welfare of this region. Research is needed to better address the current competition among the water needs of agriculture, urban and industrial uses, and natural ecosystems, and then to look at potential changes. These diverse demands on water needs in this region compound the difficulty in managing water use and projecting the impact of climate changes among the various critical sectors in this region.     

SOIL-SOILN simulations of water drainage and nitrate nitrogen transport from soil core lysimeters

Water resources protection from nitrate nitrogen (NO3-N) contamination is an important public concern and a major national environmental issue. The abilities of the SOIL-SOILN model to simulate water drainage and nitrate N fluxes from orchardgrass (Dactylis glomerata L.) were evaluated using data from a 3-yr field experiment. The soil is classified as a Hagerstown silt loam soil (fine, mixed, semiactive, mesic Typic Hapludalf). Nitrate losses below the 1-m depth from N-fertilized grazed orchardgrass were measured with intact soil core lysimeters. Five N-fertilizer treatments consisted of a control, urine application in the spring, urine application in the summer, urine application in the fall, and feces application in the summer. The SOIL-SOILN models were evaluated using water drainage and nitrate flux data for 1993-1994, 1994-1995, and 1995-1996. The N rate constants from a similar experiment with inorganic fertilizer and manure treatments under corn (Zea mays L.) were used to evaluate the SOILN model under orchardgrass sod. Results indicated that the SOIL model accurately simulated water drainage for all three years. The SOILN model adequately predicted nitrate losses for three urine treatments in each year and a control treatment in 1994-1995. However, it failed to produce accurate simulations for two control treatments in 1993-1994 and 1995-1996, and feces treatments in all three years. The inaccuracy in the simulation results for the control and feces treatments seems to be related to an inadequate modeling of N transformation processes. In general, the results demonstrate the potential of the SOILN model to predict NO3-N fluxes under pasture conditions using N transformation rate constants determined through the calibration process from corn fields on similar soils.     

Real-time quantification of mcrA, pmoA for methanogen, methanotroph estimations during composting

Composting is the controlled biological decomposition of organic matter by microorganisms during predominantly aerobic conditions. It is being increasingly adopted due to its benefits in nutrient recycling, soil reclamation, and urban land use. However, it poses an environmental concern related to its contribution to greenhouse gas production. During composting, activities of methanogenic and methanotrophic communities influence the net methane (CH4) release into the atmosphere. Using quantitative polymerase chain reaction (qPCR), this study was aimed at assessing the changes in the methyl-coenzyme M reductase (mcrA) and particulate methane monooxygenase (pmoA) copy numbers for estimation of methanogenic and methanotrophic communities, respectively. Open-windrow composting of beef cattle (Bos Taurus L.) manure with temperatures reaching > 55 degrees C was effective indegrading commensal Escherichia coli within the first week. Quantification of community DNA revealed significant differences in mcrA and pmoA copy numbers between top and middle sections. Consistent mcrA copy numbers (7.07 to 8.69 log copy number g(-1)) were detected throughout the 15-wk composting period. However, pmoA copy number varied significantly over time, with higher values during Week 0 and 1 (6.31 and 5.41 log copy number g(-1), respectively) and the lowest at Week 11 (1.6 log copy number g(-1)). Net surface CH4 emissions over the 15-wk period were correlated with higher mcrA copy number. Higher net ratio of mrA: pmoA copy numbers was observed when surface CH4 flux was high. Our results indicate that mcrA and pmoA copy numbers vary during composting and that methanogen and methanotroph populations need to be examined in conjunction with net CH4 emissions from open-windrow composting of cattle feedlot manure.     

Methane oxidation in two Swedish landfill covers measured with carbon-13 to carbon-12 isotope ratios

The release of methane (CH4) from landfills to the atmosphere and the oxidation of CH4 in the cover soils were quantified with static chambers and a 13C-isotope technique on two landfills in Sweden. One of the landfills had been closed and covered 17 years before this investigation while the other was recently covered. On both landfills, the tops of the landfills were compared with the sloping parts in the summer and winter. Emitted CH4, captured in chambers, was significantly enriched in 13C during summer compared with winter (P < 0.0001), and was enriched relative to anaerobic-zone methane. The difference between emitted and anaerobic zone delta 13C-CH4 was used to estimate soil methane oxidation. In summer, these differences ranged from 9 to 26@1000, and CH4 oxidation was estimated to be between 41 and 50% of the produced CH4 in the new landfill, and between 60 and 94% in the old landfill. In winter, when soil temperature was below 0 degree C, no difference in delta 13C was observed between emitted and anaerobic-zone CH4, suggesting that there was no soil oxidation. The temperature effect shown in this experiment suggests that there may be both seasonal and latitudinal differences in the importance of landfill CH4 oxidation. Finally the isotopic fractionation factor (alpha) varied from 1.023 to 1.038 and was temperature dependent, increasing at colder temperatures. Methanotrophic bacteria appeared to have high growth efficiencies and the majority of the methane consumed in incubations did not result in immediate CO2 production.     

Methane emissions from free-ranging cattle: comparison of tracer and integrated horizontal flux techniques

Accurate measurements of methane (CH4) emission rates from livestock in their undisturbed natural environments are required to assess their impacts on radiative forcing (i.e., enhanced greenhouse effect) and the environment. Here we compare results from two nonintrusive techniques for the measurement of CH4 emissions from cattle. The cows were kept in an outdoor feeding strip that allowed them to follow natural behavioral patterns but contained them within a well defined space. In the first technique, nitrous oxide (N2O) was released as a tracer at the upwind edge of the feeding strip, and the downwind concentrations of N2O and CH4 were measured simultaneously using Fourier transform infrared (FTIR) spectroscopy. Average CH4 emission per cow was calculated each half-hour on three separate days from the correlation between the two gases. The second technique was the integrated horizontal flux (IHF) or 1-D mass-balance method, in which we used the measured vertical profiles of CH4 concentration and windspeed downwind of the cows to determine the total CH4 emission. Comparing the IHF results to the known release rate of N2O allowed us to test the IHF technique independently. We found agreement within 10% for all comparisons on all days. The daily CH4 emission rate averaged over all tracer and IHF measurements was 342 g CH4 head(-1) d(-1). This is within the range of previous measurements for mature lactating dairy cattle (200-430 g CH4 head(-1) d(-1)) but higher than expected for yearling cattle. The high CH4 emissions are accompanied by high CO2 emissions determined from the FTIR measurements. The bias is most likely due to the measurements being made during and after supplementary feeding of the cattle.     

Comparison of DAYCENT-simulated and measured nitrous oxide emissions from a corn field

Accurate assessment of N(2)O emission from soil requires continuous year-round and spatially extensive monitoring or the use of simulation that accurately and precisely predict N(2)O fluxes based on climatic, soil, and agricultural system input data. DAYCENT is an ecosystem model that simulates, among other processes, N(2)O emissions from soils. The purpose of the study was to compare N(2)O fluxes predicted by the DAYCENT model to measured N(2)O fluxes from an experimental corn field in central Iowa. Soil water content temperature and inorganic N, simulated by DAYCENT were compared to measured values of these variables. Field N(2)O emissions were measured using four replicated automated chambers at 6-h intervals, from day of year (DOY) 42 through DOY 254 of 2006. We observed that DAYCENT generally accurately predicted soil temperature, with the exception of winter when predicted temperatures tended to be lower than measured values. Volumetric water contents predicted by DAYCENT were generally lower than measured values during most of the experimental period. Daily N(2)O emissions simulated by DAYCENT were significantly correlated to field measured fluxes; however, time series analyses indicate that the simulated fluxes were out of phase with the measured fluxes. Cumulative N(2)O emission calculated from the simulations (3.29 kg N(2)O-N ha(-1)) was in range of the measured cumulative N(2)O emission (4.26 +/- 1.09 kg N(2)O-N ha(-1)).     

Atmospheric emissions of nitrous oxide, methane, and carbon dioxide from different nitrogen fertilizers

Alternative N fertilizers that produce low greenhouse gas (GHG) emissions from soil are needed to reduce the impacts of agricultural practices on global warming potential (GWP). We quantified and compared growing season fluxes of NO, CH, and CO resulting from applications of different N fertilizer sources, urea (U), urea-ammonium nitrate (UAN), ammonium nitrate (NHNO), poultry litter, and commercially available, enhanced-efficiency N fertilizers as follows: polymer-coated urea (ESN), SuperU, UAN + AgrotainPlus, and poultry litter + AgrotainPlus in a no-till corn ( L.) production system. Greenhouse gas fluxes were measured during two growing seasons using static, vented chambers. The ESN delayed the NO flux peak by 3 to 4 wk compared with other N sources. No significant differences were observed in NO emissions among the enhanced-efficiency and traditional inorganic N sources, except for ESN in 2009. Cumulative growing season NO emission from poultry litter was significantly greater than from inorganic N sources. The NO loss (2-yr average) as a percentage of N applied ranged from 0.69% for SuperU to 4.5% for poultry litter. The CH-C and CO-C emissions were impacted by environmental factors, such as temperature and moisture, more than the N source. There was no significant difference in corn yield among all N sources in both years. Site specifics and climate conditions may be responsible for the differences among the results of this study and some of the previously published studies. Our results demonstrate that N fertilizer source and climate conditions need consideration when selecting N sources to reduce GHG emissions.     

Gas dynamics in eutrophic lake sediments affected by oxygen, nitrate, and sulfate

In many freshwater ecosystems, the contents of NO3- and SO4(2-) have increased, whereas O2 has been depleted due to the increased acid and nutrient loads. These changes may affect carbon turnover and the dynamics of the major greenhouse gases CO2, CH4, and N2O. We studied the effects of O2, NO3-, and SO4(2-) availability on carbon mineralization, and fluxes of CO2, CH4, and N2O in the sediments of hyper-eutrophic Lake Kev?t?n, Finland. Undisturbed sediment cores from the deep (9 m) and shallow (4 m) profundal were incubated in a laboratory microcosm with oxic and anoxic water flows with NO3- or SO4(2-) concentrations of 0, 30, 100, 300, and 2000 microM. The carbon mineralization rate (i.e., the sum of released CO2-C and CH4-C) was not affected by the oxidants. However, the oxidants did change the pathways of carbon degradation and the release of CH4. All of the oxidants depressed CH4 fluxes in the shallow profundal sediments, which had low organic matter content. In the deep profundal sediments rich in organic matter, the CH4 release was reduced by O2 but was not affected by SO4(2-) (the effect of NO3- was not studied). There was an increase in N2O release as the overlying water NO3- concentration increased. Anoxia and highly elevated NO3- concentrations, associated with eutrophication, increased drastically the global warming potential (GWP) of the sedimentary gases in contrast to the SO4(2-) load, which had only minor effects on the GWP.     

Greenhouse gas fluxes from an irrigated sweet corn (Zea mays L.)-potato (Solanum tuberosum L.) rotation

Intensive agriculture and increased N fertilizer use have contributed to elevated emissions of the greenhouse gases carbon dioxide (CO(2)), methane (CH(4)), and nitrous oxide (N(2)O). In this study, the exchange of CO(2), N(2)O, and CH(4) between a Quincy fine sand (mixed, mesic Xeric Torripsamments) soil and atmosphere was measured in a sweet corn (Zea mays L.)-sweet corn-potato (Solanum tuberosum L.) rotation during the 2005 and 2006 growing seasons under irrigation in eastern Washington. Gas samples were collected using static chambers installed in the second-year sweet corn and potato plots under conventional tillage or reduced tillage. Total emissions of CO(2)-C from sweet corn integrated over the season were 2071 and 1684 kg CO(2)-C ha(-1) for the 2005 and 2006 growing seasons, respectively. For the same period, CO(2) emissions from potato plots were 1571 and 1256 kg of CO(2)-C ha(-1). Cumulative CO(2) fluxes from sweet corn and potato fields were 17 and 13 times higher, respectively, than adjacent non-irrigated, native shrub steppe vegetation (NV). Nitrous oxide losses accounted for 0.5% (0.55 kg N ha(-1)) of the applied fertilizer (112 kg N ha(-1)) in corn and 0.3% (0.59 kg N ha(-1)) of the 224 kg N ha(-1) applied fertilizer. Sweet corn and potato plots, on average, absorbed 1.7 g CH(4)-C ha(-1) d(-1) and 2.3 g CH(4)-C ha(-1) d(-1), respectively. The global warming potential contributions from NV, corn, and potato fields were 459, 7843, and 6028 kg CO(2)-equivalents ha(-1), respectively, for the 2005 growing season and were 14% lower in 2006.     

Modelling air temperature gradients across managed small streams in western Washington

Leaving riparian strips on both sides of a stream is widely accepted to be an effective management approach in sustaining the valuable functions of stream and riparian ecosystems. The authors' overall objective is to provide microclimatic information for assessing the effectiveness of these strips. During the summer of 1993 and 1994, air temperatures were collected across 20 small, buffered streams in western Washington, USA, including five streams sampled before and after harvesting of the forest. These data were statistically analysed to examine the effects of adjacent harvesting with preservation of 16–72 m riparian forest strips. Regression models were developed to predict air temperatures at the stream and buffer edges, the difference between two locations, and seasonal changes. The authors found: (1) clearcutting in winter 1993/94 increased air temperature on the stream by up to 4°C, and changes in temperature variability from the stream to the upland, measured by coefficient of variation (CV), were significantly higher after harvesting; (2) forest buffers provided minimal protection for stream air temperature during the middle of summer (July) but were more effective early and late in the season; (3) buffer width was not a significant variable in predicting stream air temperature, suggesting that even a 72 m buffer was not sufficient to maintain a stream environment because of greater depth of edge influences.1998 Academic Press     

INFILTRATION OF ATRAZINE AND METABOLITES FROM A STREAM TO AN ALLUVIAL AQUIFER1

ABSTRACT: The infiltration of atrazine, deethylatrazine, and deisopropylatrazine from Walnut Creek, a tributary stream, to the alluvial valley aquifer along the South Skunk River in central Iowa occurred where the stream transects the river's flood plain. A preliminary estimate indicated that the infiltration was significant and warrants further investigation. Infiltration was estimated by measuring the loss of stream discharge in Walnut Creek and the concentrations of atrazine and its metabolites deethylatrazine and deisopropylatrazine, in ground water 1 m beneath the streambed. Infiltration was estimated before application of agrichemicals to the fields during a dry period on April 7, 1994, and after application of agrichemicals during a period of small runoff on June 8, 1994. On April 7, the flux of atrazine, deethylatrazine, and deisopropylatrazine from Walnut Creek into the alluvial valley aquifer ranged from less than 10 to 60 (μg/d)/m², whereas on June 8 an increased flux ranged from 270 to 3060 (μg/d)/m². By way of comparison, the calculated fluxes of atrazine beneath Walnut Creek, for these two dates, were two to five orders of magnitude greater than an estimated flux of atrazine to ground water caused by leaching from a field on a per-unit-area basis. Furthermore, the unit-area flux rates of water from Walnut Creek to the alluvial valley aquifer were about three orders of magnitude greater than estimated recharge to the alluvial aquifer from precipitation. The large flux of chemicals from Walnut Creek to the alluvial valley aquifer was due in part to the conductive streambed and rather fast ground water velocities; average vertical hydraulic conductivity through the streambed was calculated as 35 and 90 m/d for the two sampling dates, and estimated ground water velocities ranged from 1 to 5 m/d.     

Nitrogen oxide and methane emissions under varying tillage and fertilizer management

Comprehensive assessment of the total greenhouse gas (GHG) budget of reduced tillage agricultural systems must consider emissions of nitrous oxide (N2O) and methane (CH4), each of which have higher global warming potentials than carbon dioxide (CO2). Tillage intensity may also impact nitric oxide (NO) emissions, which can have various environmental and agronomic impacts. In 2003 and 2004, we used chambers to measure N2O, CH4, and NO fluxes from plots that had been managed under differing tillage intensity since 1991. The effect of tillage on non-CO2 GHG emissions varied, in both magnitude and direction, depending on fertilizer practices. Emissions of N2O following broadcast urea (BU) application were higher under no till (NT) and conservation tillage (CsT) compared to conventional tillage (CT). In contrast, following anhydrous ammonia (AA) injection, N2O emissions were higher under CT and CsT compared to NT. Emissions following surface urea ammonium nitrate (UAN) application did not vary with tillage. Total growing season non-CO2 GHG emissions were equivalent to CO2 emissions of 0.15 to 1.9 Mg CO2 ha(-1) yr(-1) or 0.04 to 0.53 Mg soil-C ha(-1) yr(-1). Emissions of N2O from AA-amended plots were two to four times greater than UAN- and BU-amended plots. Total NO + N2O losses in the UAN treatment were approximately 50% lower than AA and BU. This study demonstrates that N2O emissions can represent a substantial component of the total GHG budget of reduced tillage systems, and that interactions between fertilizer and tillage practices can be important in controlling non-CO2 GHG emissions.     

Passive flux meter measurement of water and nutrient flux in saturated porous media: bench-scale laboratory tests

The passive nutrient flux meter (PNFM) is introduced for simultaneous measurement of both water and nutrient flux through saturated porous media. The PNFM comprises a porous sorbent pre-equilibrated with a suite of alcohol tracers, which have different partitioning coefficients. Water flux was estimated based on the loss of loaded resident tracers during deployment, while nutrient flux was quantified based on the nutrient solute mass captured on the sorbent. An anionic resin, Lewatit 6328 A, was used as a permeable sorbent and phosphate (PO4(3-)) was the nutrient studied. The phosphate sorption capacity of the resin was measured in batch equilibration tests as 56 mg PO4(3-) g(-1), which was determined to be adequate capacity to retain PO4(3-) loads intercepted over typical PNFM deployment periods in most natural systems. The PNFM design was validated with bench-scale laboratory tests for a range of 9.8 to 28.3 cm d(-1) Darcy velocities and 6 to 43 h deployment durations. Nutrient and water fluxes measured by the PNFM averaged within 6 and 12% of the applied values, respectively, indicating that the PNFM shows promise as a tool for simultaneous measurement of water and nutrient fluxes.