Emission of the greenhouse gases nitrous oxide and methane from constructed wetlands in europe

The potential atmospheric impact of constructed wetlands (CWs) should be examined as there is a worldwide increase in the development of these systems. Fluxes of N(2)O, CH(4), and CO(2) have been measured from CWs in Estonia, Finland, Norway, and Poland during winter and summer in horizontal and vertical subsurface flow (HSSF and VSSF), free surface water (FSW), and overland and groundwater flow (OGF) wetlands. The fluxes of N(2)O-N, CH(4)-C, and CO(2)-C ranged from -2.1 to 1000, -32 to 38 000, and -840 to 93 000 mg m(-2) d(-1), respectively. Emissions of N(2)O and CH(4) were significantly higher during summer than during winter. The VSSF wetlands had the highest fluxes of N(2)O during both summer and winter. Methane emissions were highest from the FSW wetlands during wintertime. In the HSSF wetlands, the emissions of N(2)O and CH(4) were in general highest in the inlet section. The vegetated ponds in the FSW wetlands released more N(2)O than the nonvegetated ponds. The global warming potential (GWP), summarizing the mean N(2)O and CH(4) emissions, ranged from 5700 to 26000 and 830 to 5100 mg CO(2) equivalents m(-2) d(-1) for the four CW types in summer and winter, respectively. The wintertime GWP was 8.5 to 89.5% of the corresponding summertime GWP, which highlights the importance of the cold season in the annual greenhouse gas release from north temperate and boreal CWs. However, due to their generally small area North European CWs were suggested to represent only a minor source for atmospheric N(2)O and CH(4).     

Greenhouse gases in non-oxygenated and artificially oxygenated eutrophied lakes during winter stratification

Concentrations of dissolved methane (CH4), carbon dioxide (CO2), and nitrous oxide (N2O) were measured in the water columns of non-oxygenated and artificially oxygenated, ice-covered eutrophied lakes in the mid-boreal zone in Finland during late winter 1997 and 1999. Sampling was conducted during winter stratification, the critical period for oxygen (O2) deficiency in seasonally ice-covered, thermally stratified lakes. Oxygen concentrations were maintained at least at a moderate level throughout the oxygenated water columns, whereas the non-oxygenated columns suffered anoxic hypolimnia. The mean concentrations of dissolved CH4 exceeding the atmospheric equilibrium were greater in the non-oxygenated water columns (20.6-154 microM) than in the oxygenated ones (0.01-1.41 microM). In contrast, the mean excess CO2 concentrations varied less between the non-oxygenated and oxygenated sites (0.28-0.47 and 0.25-0.31 mM, respectively). Oxygenated water columns had greater mean excess concentrations of N2O (0.018-0.032 microM) than the non-oxygenated ones (0.005-0.024 microM). If the accumulated greenhouse gas stores in the water columns during winter are assumed to be released to the atmosphere during the spring overturn, the global warming potentials (GWP, time horizon 100 yr) of these potential emissions at the non-oxygenated, eutrophic study sites ranged from 177 to 654 g CO2 equivalent (CO2-e) m-2 compared with 144 to 173 g CO2-e m-2 at the oxygenated sites. The increase in the accumulation of CH4 was the main reason for the higher GWP of the non-oxygenated sites. Anthropogenic eutrophication of lake ecosystems can generate increased CH4 emissions due to associated O2 depletion of their sediment and water column.     

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.     

Net global warming potential and greenhouse gas intensity in irrigated cropping systems in northeastern Colorado

The impact of management on global warming potential (GWP), crop production, and greenhouse gas intensity (GHGI) in irrigated agriculture is not well documented. A no-till (NT) cropping systems study initiated in 1999 to evaluate soil organic carbon (SOC) sequestration potential in irrigated agriculture was used in this study to make trace gas flux measurements for 3 yr to facilitate a complete greenhouse gas accounting of GWP and GHGI. Fluxes of CO2, CH4, and N2O were measured using static, vented chambers, one to three times per week, year round, from April 2002 through October 2004 within conventional-till continuous corn (CT-CC) and NT continuous corn (NT-CC) plots and in NT corn-soybean rotation (NT-CB) plots. Nitrogen fertilizer rates ranged from 0 to 224 kg N ha(-1). Methane fluxes were small and did not differ between tillage systems. Nitrous oxide fluxes increased linearly with increasing N fertilizer rate each year, but emission rates varied with years. Carbon dioxide efflux was higher in CT compared to NT in 2002 but was not different by tillage in 2003 or 2004. Based on soil respiration and residue C inputs, NT soils were net sinks of GWP when adequate fertilizer was added to maintain crop production. The CT soils were smaller net sinks for GWP than NT soils. The determinant for the net GWP relationship was a balance between soil respiration and N2O emissions. Based on soil C sequestration, only NT soils were net sinks for GWP. Both estimates of GWP and GHGI indicate that when appropriate crop production levels are achieved, net CO2 emissions are reduced. The results suggest that economic viability and environmental conservation can be achieved by minimizing tillage and utilizing appropriate levels of fertilizer.     

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.     

Emission of CO2, CH4 and N2O from freshwater marsh in northeast of China

The wetlands play an important role in carbon storage, especially at high latitudes, at which they store nearly one-third of global soil carbons. However, few studies have investigated the emissions of CO(2), CH(4) and N(2)O in the long-term, especially effects of freeze-thaw cycles on these gases emissions in freshwater marsh ecosystems. In this paper, we collected greenhouse gas emission data from a freshwater marsh area in China for 4 years, evaluated their release variables and speculated on their potential atmospheric impact. For this paper, we report on the CO(2), CH(4) and N(2)O emission rates recorded from June 2002 to November 2005 in the Sanjiang Plain of northeast China. We measured their interannual variations and fluctuations, as well as factors affecting their emissions, and estimated their regulation and freeze-thaw cycle impacts. Our results revealed obvious CO(2) and CH(4) emission fluctuations during the winter months, and during the freeze-thaw cycle, and a strong interannual variation during the growing season. Overall, we documented a close relationship between the CO(2) and CH(4) emissions, implicating some regulatory commonality. We determined that the marsh was a N(2)O sink during the winter, but a significant source of N(2)O during the freeze-thaw cycle as the temperature increased, especially in early summer. During the thaw-freeze period, the N(2)O levels were positively correlated with the water depth. Additionally, water depth greatly governed the interannual variation of the N(2)O emissions from the marshes during the thaw-freeze period.     

Greenhouse gas emissions and soil indicators four years after manure and compost applications

Understanding how carbon, nitrogen, and key soil attributes affect gas emissions from soil is crucial for alleviating their undesirable residual effects that can linger for years after termination of manure and compost applications. This study was conducted to evaluate the emission of soil CO2, N2O, and CH4 and soil C and N indicators four years after manure and compost application had stopped. Experimental plots were treated with annual synthetic N fertilizer (FRT), annual and biennial manure (MN1 and MN2, respectively), and compost (CP1 and CP2, respectively) from 1992 to 1995 based on removal of 151 kg N ha(-1) yr(-1) by continuous corn (Zea mays L.). The control (CTL) plots received no input. After 1995, only the FRT plots received N fertilizer in the spring of 1999. In 1999, the emissions of CO2 were similar between control and other treatments. The average annual carbon input in the CTL and FRT plots were similar to soil CO2-C emission (4.4 and 5.1 Mg C ha(-1) yr(-1), respectively). Manure and compost resulted in positive C and N balances in the soil four years after application. Fluxes of CH4-C and N2O-N were nearly zero, which indicated that the residual effects of manure and compost four years after application had no negative influence on soil C and N storage and global warming. Residual effects of compost and manure resulted in 20 to 40% higher soil microbial biomass C, 42 to 74% higher potentially mineralizable N, and 0.5 unit higher pH compared with the FRT treatment. Residual effects of manure and compost on CO2, N20, and CH4 emissions were minimal and their benefits on soil C and N indicators were more favorable than that of N fertilizer.     

3,4-Dimethylpyrazol phosphate effect on nitrous oxide, nitric oxide, ammonia, and carbon dioxide emissions from grasslands

Intensively managed grasslands are potentially a large source of NH3, N2O, and NO emissions because of the large input of nitrogen (N) in fertilizers. Addition of nitrification inhibitors (NI) to fertilizers maintains soil N in ammonium form. Consequently, N2O and NO losses are less likely to occur and the potential for N utilization is increased, and NH3 volatilization may be increased. In the present study, we evaluated the effectiveness of the nitrification inhibitor 3,4-dimethylpyrazol phosphate (DMPP) on NH3, N2O, NO, and CO2 emissions following the application of 97 kg N ha(-1) as ammonium sulfate nitrate (ASN) and 97 kg NH4+ -N ha(-1) as cattle slurry to a mixed clover-ryegrass sward in the Basque Country (northern Spain). After slurry application, 16.0 and 0.7% of the NH4+ -N applied was lost in the form of N2O and NO, respectively. The application of DMPP induced a decrease of 29 and 25% in N2O and NO emissions, respectively. After ASN application 4.6 and 2.8% of the N applied was lost as N2O and NO, respectively. The application of DMPP with ASN (as ENTEC 26; COMPO, Münster, Germany) unexpectedly did not significantly reduce N2O emissions, but induced a decrease of 44% in NO emissions. The amount of NH4+ -N lost in the form of NH3 following slurry and slurry + DMPP applications was 7.8 and 11.0%, respectively, the increase induced by DMPP not being statistically significant. Levels of CO2 emissions were unaffected in all cases by the use of DMPP. We conclude that DMPP is an efficient nitrification inhibitor to be used to reduce N2O and NO emissions from grasslands.     

Carbon, nitrogen balances and greenhouse gas emission during cattle feedlot manure composting

Carbon and N losses reduce the agronomic value of compost and contribute to greenhouse gas (GHG) emissions. This study investigated GHG emissions during composting of straw-bedded manure (SBM) and wood chip-bedded manure (WBM). For SBM, dry matter (DM) loss was 301 kg Mg(-1), total carbon (TC) loss was 174 kg Mg(-1), and total nitrogen (TN) loss was 8.3 kg Mg(-1). These correspond to 30.1% of initial DM, 52.8% of initial TC, and 41.6% of initial TN. For WBM, DM loss was 268 kg Mg(-1), TC loss was 154 kg Mg(-1), and TN loss was 1.40 kg Mg(-1), corresponding to 26.5, 34.5, and 11.8% of initial amounts. Most C was lost as CO2 with CH4 accounting for <6%. However, the net contribution to greenhouse gas emissions was greater for CH4 since it is 21 times more effective at trapping heat than CO2. Nitrous oxide (N2O) emissions were 0.077 kg N Mg(-1) for SBM and 0.084 kg N Mg(-1) for WBM, accounting for 1 to 6% of total N loss. Total GHG emissions as CO2-C equivalent were not significantly different between SBM (368.4 +/- 18.5 kg Mg(-1)) and WBM (349.2 +/- 24.3 kg Mg(-1)). However, emission of 368.4 kg C Mg(-1) (CO2-C equivalent) was greater than the initial TC content (330.5 kg Mg(-1)) of SBM, raising the question of the net benefits of composting on C sequestration. Further study is needed to evaluate the impact of composting on overall GHG emissions and C sequestration and to fully investigate livestock manure management options.     

Emissions of ammonia, methane, carbon dioxide, and nitrous oxide from dairy cattle housing and manure management systems

Concentrated animal feeding operations emit trace gases such as ammonia (NH?), methane (CH?), carbon dioxide (CO?), and nitrous oxide (N?O). The implementation of air quality regulations in livestock-producing states increases the need for accurate on-farm determination of emission rates. The objective of this study was to determine the emission rates of NH?, CH?, CO?, and N?O from three source areas (open lots, wastewater pond, compost) on a commercial dairy located in southern Idaho. Gas concentrations and wind statistics were measured each month and used with an inverse dispersion model to calculate emission rates. Average emissions per cow per day from the open lots were 0.13 kg NH?, 0.49 kg CH?, 28.1 kg CO?, and 0.01 kg N?O. Average emissions from the wastewater pond (g m(-2) d(-1)) were 2.0 g NH?, 103 g CH?, 637 g CO?, and 0.49 g N?O. Average emissions from the compost facility (g m(-2) d(-1)) were 1.6 g NH?, 13.5 g CH?, 516 g CO?, and 0.90 g N?O. The combined emissions of NH?, CH?, CO?, and N?O from the lots, wastewater pond and compost averaged 0.15, 1.4, 30.0, and 0.02 kg cow(-1) d(-1), respectively. The open lot areas generated the greatest emissions of NH?, CO?, and N?O, contributing 78, 80, and 57%, respectively, to total farm emissions. Methane emissions were greatest from the lots in the spring (74% of total), after which the wastewater pond became the largest source of emissions (55% of total) for the remainder of the year. Data from this study can be used to develop trace gas emissions factors from open-lot dairies in southern Idaho and potentially other open-lot production systems in similar climatic regions.     

Matrix based fertilizers reduce nitrogen and phosphorus leaching in three soils

We compared the efficacy of matrix based fertilizers (MBFs) formulated to reduce NO3-, NH4+, and total phosphorus (TP) leaching, with Osmocoate 14-14-14, a conventional commercial slow release fertilizer (SRF) and an unamended control in three different soil textures in a greenhouse column study. The MBFs covered a range of inorganic N and P in compounds that are relatively loosely bound (MBF 1) to more moderately bound (MBF 2) and more tightly bound compounds (MBF 3) mixed with Al(SO4)3H2O and/or Fe2(SO4)3 and with high ionic exchange compounds starch, chitosan and lignin. When N and P are released, the chemicals containing these nutrients in the MBF bind N and P to a Al(SO4)3H2O and/or Fe2(SO4)3 starch-chitosan-lignin matrix. One milligram (8000 spores) of Glomus intradices was added to all formulations to enhance nutrient uptake. In all three soil textures the SRF leachate contained a higher amount of NH4+, NO3- and TP than leachate from all other fertilizers. In all three soils there were no consistent differences in the amount of NH4+, NO3- and TP in the MBF leachates compared to the control leachate. Plants growing in soils receiving SRF had greater shoot, root and total biomass than all MBFs regardless of Al(SO4)3H2O or Fe2(SO4)3 additions. Arbuscular mycorrhizal infection in plant roots did not consistently differ among plants growing in soil receiving SRF, MBFs and control treatments. Although the MBFs resulted in less plant growth in this experiment they may be applied to soils growing plants in areas that are at high risk for nutrient leaching to surface waters.     

Greenhouse gas emissions during co-composting of calf mortalities with manure

Composting may be a viable on-farm option for disposal of cattle carcasses. This study investigated greenhouse gas emissions during co-composting of calf mortalities with manure. Windrows were constructed that contained manure + straw (control compost [CK]) or manure + straw + calf mortalities (CM) using two technologies: a tractor-mounted front-end loader or a shredder bucket. Composting lasted 289 d. The windrows were turned twice (on Days 72 and 190), using the same technology used in their creation. Turning technology had no effect on greenhouse gas emissions or the properties of the final compost. The CO2 (75.2 g d(-1) m(-2)), CH4 (2.503 g d(-1) m(-2)), and N2O (0.370 g d(-1) m(-2)) emissions were higher (p < 0.05) in CM than in CK (25.7, 0.094, and 0.076 g d(-1) m(-2) for CO2, CH4, and N2O, respectively), which reflected differences in materials used to construct the compost windrows and therefore their total C and total N contents. The final CM compost had higher (p < 0.05) total N, total C, and mineral N content (NO3*+ NO2* + NH4+) than did CK compost and therefore has greater agronomic value as a fertilizer.     

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.     

Transport and fate of nitrate in a glacial outwash aquifer in relation to ground water age,land use practices,and redox processes

A combination of ground water modeling, chemical and dissolved gas analyses, and chlorofluorocarbon age dating of water was used to determine the relation between changes in agricultural practices, and NO3- concentrations in ground water of a glacial outwash aquifer in west-central Minnesota. The results revealed a redox zonation throughout the saturated zone with oxygen reduction occurring near the water table, NO3- reduction immediately below it, and then a large zone of ferric iron reduction, with a small area of sulfate (SO4(2-)) reduction and methanogenesis (CH4) near the end of the transsect. Analytical and NETPATH modeling results supported the hypothesis that organic carbon served as the electron donor for the redox reactions. Denitrification rates were quite small, 0.005 to 0.047 mmol NO3- yr(-1), and were limited by the small amounts of organic carbon, 0.01 to 1.45%. In spite of the organic carbon limitation, denitrification was virtually complete because residence time is sufficient to allow even slow processes to reach completion. Ground water sample ages showed that maximum residence times were on the order of 50 to 70 yr. Reconstructed NO3- concentrations, estimated from measured NO3- and dissolved N gas showed that NO3- concentrations have been increasing in the aquifer since the 1940s, and have been above the 714 micromol L(-1) maximum contaminant level at most sites since the mid- to late-1960s. This increase in NO3- has been accompanied by a corresponding increase in agricultural use of fertilizer, identified as the major source of NO3- to the aquifer.     

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.     

Dissolved organic carbon dynamics in a riparian aquifer: effects of hydrology and nitrate enrichment

The capacity of riparian soils to remove nitrate (NO3) from ground water is well established, but the effects of ground water NO3(-)-enrichment on C dynamics are not well studied. We incubated horizontal cores of aquifer material extracted from beneath moderately well-drained (MWD) and poorly drained (PD) soils in a riparian forest in Rhode Island, USA for 132 d, and dosed (flow rate, 170 mL d(-1); dissolved O2, 2 in PD and 5 mg L(-1) in MWD cores) with ground water amended with either Br-, Br(-)+ NO3- (10 mg N L(-1)), or Br(-) + NO3(-) + DOC (20 mg C L(-1)). The DOC was extracted from forest floor material and added during the first 56 d of the experiment. Addition of NO3- had limited effect on CO2 production while DOC amendment had a significant effect in the PD but not in the MWD mesocosms. Total CO2 production (mg CO2-C kg(-1) soil) was 6.3, 7.0, and 10.1 in the PD and 3.6, 4.0, and 4.5 in the MWD cores amended with Br-, Br(-) + NO3-, and Br(-) + NO3(-) + DOC, respectively. Carbon balance (C(bal) = DOC(in) - (DOC(out) + CO2-C) showed a net C retention of 8.0 mg C kg(-1) soil in the DOC-amended MWD cores (equivalent to 50% of the DOC added), and a net C loss of 8.3 mg C kg(-1) soil in similarly treated PD cores. The lack of C retention in the PD cores was ascribed to reductive dissolution of minerals implicated in DOC sorption. These findings underscore that there is marked variation in C dynamics in riparian aquifers that has the potential to influence the fate of NO3- and DOC in the landscape.     

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.     

Leachability and phytoavailability of nitrogen, phosphorus, and potassium from different bio-composts under chloride- and sulfate-dominated irrigation water

Concerns over increased phosphorus (P) application with nitrogen (N)-based compost application have shifted the trend to P-based composed application, but focusing on one or two nutritional elements does not serve the goals of sustainable agriculture. The need to understand the nutrient release and uptake from different composts has been further aggravated by the use of saline irrigation water in the recent scenario of fresh water shortage. Therefore, we evaluated the leachability and phytoavailability of P, N, and K from a sandy loam soil amended with animal, poultry, and sludge composts when applied on a total P-equivalent basis (200 kg ha(-1)) under Cl(-) (NaCl)- and SO4(2-) (Na2SO4)-dominated irrigation water. Our results showed that the concentration of dissolved reactive P (DRP) was higher in leachates under SO(4)(2-) than Cl(-) treatments. Compost amendments differed for DRP leaching in the following pattern: sludge > animal > poultry > control. Maize (Zea mays L.) growth and P uptake were severely suppressed under Cl(-) irrigation compared with SO4(2-) and non-saline treatments. All composts were applied on a total P-equivalent basis, but maximum plant (shoot + root) P uptake was observed under sludge compost amendment (73.4 mg DW(-1)), followed by poultry (39.3 mg DW(-1)), animal (15.0 mg DW(-1)), and control (1.2 mg DW(-1)) treatment. Results of this study reveal that irrigation water dominated by SO4(2-) has greater ability to replace/leach P, other anions (NO3(-)), and cations (K+). Variability in P release from different bio-composts applied on a total P-equivalent basis suggested that P availability is highly dependent on compost source.     

Greenhouse gas emissions from two soils receiving nitrogen fertilizer and swine manure slurry

The interactive effects of soil texture and type of N fertility (i.e., manure vs. commercial N fertilizer) on N(2)O and CH(4) emissions have not been well established. This study was conducted to assess the impact of soil type and N fertility on greenhouse gas fluxes (N(2)O, CH(4), and CO(2)) from the soil surface. The soils used were a sandy loam (789 g kg(-1) sand and 138 g kg(-1) clay) and a clay soil (216 g kg(-1) sand, and 415 g kg(-1) clay). Chamber experiments were conducted using plastic buckets as the experimental units. The treatments applied to each soil type were: (i) control (no added N), (ii) urea-ammonium nitrate (UAN), and (iii) liquid swine manure slurry. Greenhouse gas fluxes were measured over 8 weeks. Within the UAN and swine manure treatments both N(2)O and CH(4) emissions were greater in the sandy loam than in the clay soil. In the sandy loam soil N(2)O emissions were significantly different among all N treatments, but in the clay soil only the manure treatment had significantly higher N(2)O emissions. It is thought that the major differences between the two soils controlling both N(2)O and CH(4) emissions were cation exchange capacity (CEC) and percent water-filled pore space (%WFPS). We speculate that the higher CEC in the clay soil reduced N availability through increased adsorption of NH(4)(+) compared to the sandy loam soil. In addition the higher average %WFPS in the sandy loam may have favored higher denitrification and CH(4) production than in the clay soil.     

Greenhouse gas emissions during cattle feedlot manure composting

The emission of greenhouse gases (GHG) during feedlot manure composting reduces the agronomic value of the final compost and increases the greenhouse effect. A study was conducted to determine whether GHG emissions are affected by composting method. Feedlot cattle manure was composted with two aeration methods--passive (no turning) and active (turned six times). Carbon lost in the forms of CO2 and CH4 was 73.8 and 6.3 kg C Mg-1 manure for the passive aeration treatment and 168.0 and 8.1 kg C Mg-1 manure for the active treatment. The N loss in the form of N2O was 0.11 and 0.19 kg N Mg-1 manure for the passive and active treatments. Fuel consumption to turn and maintain the windrow added a further 4.4 kg C Mg-1 manure for the active aeration treatment. Since CH4 and N2O are 21 and 310 times more harmful than CO2 in their global warming effect, the total GHG emission expressed as CO2-C equivalent was 240.2 and 401.4 kg C Mg-1 manure for passive and active aeration. The lower emission associated with the passive treatment was mainly due to the incomplete decomposition of manure and a lower gas diffusion rate. In addition, turning affected N transformation and transport in the window profile, which contributed to higher N2O emissions for the active aeration treatment. Gas diffusion is an important factor controlling GHG emissions. Higher GHG concentrations in compost windrows do not necessarily mean higher production or emission rates.