scholarly journals Combining two complementary micrometeorological methods to measure CH<sub>4</sub> and N<sub>2</sub>O fluxes over pasture

2016 ◽  
Vol 13 (4) ◽  
pp. 1309-1327 ◽  
Author(s):  
Johannes Laubach ◽  
Matti Barthel ◽  
Anitra Fraser ◽  
John E. Hunt ◽  
David W. T. Griffith
Keyword(s):  
Large Fraction ◽  
Industrial Sector ◽  
N2o Emissions ◽  
Emission Rates ◽  
Co2 Fluxes ◽  
Nitrogen Inputs ◽  
Animal Excreta ◽  
N2o Fluxes ◽  
Ch4 And N2o ◽  
Carbon Dioxide Co2

Abstract. New Zealand's largest industrial sector is pastoral agriculture, giving rise to a large fraction of the country's emissions of methane (CH4) and nitrous oxide (N2O). We designed a system to continuously measure CH4 and N2O fluxes at the field scale on two adjacent pastures that differed with respect to management. At the core of this system was a closed-cell Fourier transform infrared (FTIR) spectrometer, which measured the mole fractions of CH4, N2O and carbon dioxide (CO2) at two heights at each site. In parallel, CO2 fluxes were measured using eddy-covariance instrumentation. We applied two different micrometeorological ratio methods to infer the CH4 and N2O fluxes from their respective mole fractions and the CO2 fluxes. The first is a variant of the flux-gradient method, where it is assumed that the turbulent diffusivities of CH4 and N2O equal that of CO2. This method was reliable when the CO2 mole-fraction difference between heights was at least 4 times greater than the FTIR's resolution of differences. For the second method, the temporal increases of mole fractions in the stable nocturnal boundary layer, which are correlated for concurrently emitted gases, are used to infer the unknown fluxes of CH4 and N2O from the known flux of CO2. This method was sensitive to “contamination” from trace gas sources other than the pasture of interest and therefore required careful filtering. With both methods combined, estimates of mean daily CH4 and N2O fluxes were obtained for 56 % of days at one site and 73 % at the other. Both methods indicated both sites as net sources of CH4 and N2O. Mean emission rates for 1 year at the unfertilised, winter-grazed site were 8.9 (±0.79) nmol CH4 m−2 s−1 and 0.38 (±0.018) nmol N2O m−2 s−1. During the same year, mean emission rates at the irrigated, fertilised and rotationally grazed site were 8.9 (±0.79) nmol CH4 m−2 s−1 and 0.58 (±0.020) nmol N2O m−2 s−1. At this site, the N2O emissions amounted to 1.21 (±0.15) % of the nitrogen inputs from animal excreta and fertiliser application.

scholarly journals Combining two complementary micrometeorological methods to measure CH<sub>4</sub> and N<sub>2</sub>O fluxes over pasture

2015 ◽  
Vol 12 (18) ◽  
pp. 15245-15299 ◽  
Author(s):  
J. Laubach ◽  
M. Barthel ◽  
A. Fraser ◽  
J. E. Hunt ◽  
D. W. T. Griffith
Keyword(s):  
Large Fraction ◽  
Industrial Sector ◽  
N2o Emissions ◽  
Emission Rates ◽  
Co2 Fluxes ◽  
Nitrogen Inputs ◽  
Animal Excreta ◽  
N2o Fluxes ◽  
Ch4 And N2o ◽  
Carbon Dioxide Co2

Abstract. New Zealand's largest industrial sector is pastoral agriculture, giving rise to a large fraction of the country's emissions of methane (CH4) and nitrous oxide (N2O). We designed a system to continuously measure CH4 and N2O fluxes at the field scale on two adjacent pastures that differed with respect to management. At the core of this system was a closed-cell Fourier-transform infrared spectrometer (FTIR), measuring the mole fractions of CH4, N2O and carbon dioxide (CO2) at two heights at each site. In parallel, CO2 fluxes were measured using eddy-covariance instrumentation. We applied two different micrometeorological ratio methods to infer the CH4 and N2O fluxes from their respective mole fractions and the CO2 fluxes. The first is a variant of the flux-gradient method, where it is assumed that the turbulent diffusivities of CH4 and N2O equal that of CO2. This method was reliable when the CO2 mole-fraction difference between heights was at least 4 times greater than the FTIR's resolution of differences. For the second method, the temporal increases of mole fractions in the stable nocturnal boundary layer, which are correlated for concurrently-emitted gases, are used to infer the unknown fluxes of CH4 and N2O from the known flux of CO2. This method was sensitive to "contamination" from trace gas sources other than the pasture of interest and therefore required careful filtering. With both methods combined, estimates of mean daily CH4 and N2O fluxes were obtained for 60 % of days at one site and 77 % at the other. Both methods indicated both sites as net sources of CH4 and N2O. Mean emission rates for one year at the unfertilised, winter-grazed site were 8.2 (± 0.91) nmol CH4 m−2 s−1 and 0.40 (± 0.018) nmol N2O m−2 s−1. During the same year, mean emission rates at the irrigated, fertilised and rotationally-grazed site were 7.0 (± 0.89) nmol CH4 m−2 s−1 and 0.57 (± 0.019) nmol N2O m−2 s−1. At this site, the N2O emissions amounted to 1.19 (± 0.15) % of the nitrogen inputs from animal excreta and fertiliser application.

scholarly journals Water Salinity Should Be Reduced for Irrigation to Minimize Its Risk of Increased Soil N2O Emissions

2018 ◽  
Vol 15 (10) ◽  
pp. 2114 ◽  
Author(s):  
Qi Wei ◽  
Junzeng Xu ◽  
Linxian Liao ◽  
Yawei Li ◽  
Haiyu Wang ◽  
...  
Keyword(s):  
Saline Water ◽  
N2o Emission ◽  
Salinity Level ◽  
N2o Emissions ◽  
Low Salinity ◽  
Nitrogen Inputs ◽  
Salinity Levels ◽  
N2o Fluxes ◽  
Moisture Dynamics ◽  
Irrigated Soils

To reveal the effect of irrigation salinity on soil nitrous oxide (N2O) emission, pot experiments were designed with three irrigation salinity levels (NaCl and CaCl2 of 1, 2.5 and 4 g/L equivalence, Ec = 3.6, 8.1 and 12.7 ds/m), either for 0 kg N/ha (N0) or 120 kg N/ha (N120) nitrogen inputs. N2O emissions from soils irrigated at different salinity levels varied in a similar pattern which was triggered by soil moisture dynamics. Yet, the magnitudes of pulse N2O fluxes were significantly varied, with the peak flux at 5 g/L irrigation salinity level being much higher than at 2 and 8 g/L. Compared to fresh water irrigated soils, cumulative N2O fluxes were reduced by 22.7% and 39.6% (N0), 29.1% and 39.2% (N120) for soils irrigated with 2 and 8 g/L saline water, while they were increased by 87.7% (N0) and 58.3% (N120) for soils irrigated with 5 g/L saline water. These results suggested that the effect degree of salinity on consumption and production of N2O might vary among irrigation salinity ranges. As such, desalinating brackish water to a low salinity level (such as 2 g/L) before it is used for irrigation might be helpful for solving water resources crises and mitigating soil N2O emissions.

scholarly journals Automatic high-frequency measurements of full soil greenhouse gas fluxes in a tropical forest

2018 ◽  
Author(s):  
Elodie Alice Courtois ◽  
Clément Stahl ◽  
Benoit Burban ◽  
Joke Van den Berge ◽  
Daniel Berveiller ◽  
...  
Keyword(s):  
High Frequency ◽  
Co2 Flux ◽  
Appropriate Technology ◽  
Flux Chamber ◽  
Soil Co2 Flux ◽  
Reliable Estimation ◽  
Closure Time ◽  
N2o Fluxes ◽  
Ch4 And N2o ◽  
Carbon Dioxide Co2

Abstract. Measuring in situ soil fluxes of carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O) continuously at high frequency requires appropriate technology. We tested the combination of a commercial automated soil CO2 flux chamber system (LI-8100A) with a CH4 and N2O analyzer (Picarro G2308) in a tropical rainforest for 4 months. A chamber closure time of 2 minutes was sufficient for a reliable estimation of CO2 and CH4 fluxes (100 % and 98.5 % of fluxes were above Minimum Detectable Flux – MDF, respectively). This closure time was generally not suitable for a reliable estimation of the low N2O fluxes in this ecosystem but was sufficient for detecting rare major peak events. A closure time of 25 minutes was more appropriate for reliable estimation of most N2O fluxes (85.6 % of measured fluxes are above MDF ± 0.002 nmol m−2 s−1). Our study highlights the importance of adjusted closure time for each gas.

scholarly journals Methane and nitrous oxide sources and emissions in a subtropical freshwater reservoir, South East Queensland, Australia

2014 ◽  
Vol 11 (18) ◽  
pp. 5245-5258 ◽  
Author(s):  
K. Sturm ◽  
Z. Yuan ◽  
B. Gibbes ◽  
U. Werner ◽  
A. Grinham
Keyword(s):  
Nitrous Oxide ◽  
Water Column ◽  
Water Flux ◽  
No Production ◽  
Pore Waters ◽  
Ch4 Production ◽  
N2o Fluxes ◽  
Ch4 And N2o ◽  
Diffusive Fluxes ◽  
Carbon Dioxide Co2

Abstract. Reservoirs have been identified as an important source of non-carbon dioxide (CO2) greenhouse gases with wide ranging fluxes for reported methane (CH4); however, fluxes for nitrous oxide (N2O) are rarely quantified. This study investigates CH4 and N2O sources and emissions in a subtropical freshwater Gold Creek Reservoir, Australia, using a combination of water–air and sediment–water flux measurements and water column and pore water analyses. The reservoir was clearly a source of these gases as surface waters were supersaturated with CH4 and N2O. Atmospheric CH4 fluxes were dominated by ebullition (60 to 99%) relative to diffusive fluxes and ranged from 4.14 × 102 to 3.06 × 105 μmol CH4 m−2 day−1 across the sampling sites. Dissolved CH4 concentrations were highest in the anoxic water column and sediment pore waters (approximately 5 000 000% supersaturated). CH4 production rates of up to 3616 ± 395 μmol CH4 m−2 day−1 were found during sediment incubations in anoxic conditions. These findings are in contrast to N2O where no production was detected during sediment incubations and the highest dissolved N2O concentrations were found in the oxic water column which was 110 to 220% supersaturated with N2O. N2O fluxes to the atmosphere were primarily through the diffusive pathway, mainly driven by diffusive fluxes from the water column and by a minor contribution from sediment diffusion and ebullition. Results suggest that future studies of subtropical reservoirs should monitor CH4 fluxes with an appropriate spatial resolution to ensure capture of ebullition zones, whereas assessment of N2O fluxes should focus on the diffusive pathway.

scholarly journals High methane emissions dominated annual greenhouse gas balances 30 years after bog rewetting

2015 ◽  
Vol 12 (14) ◽  
pp. 4361-4371 ◽  
Author(s):  
M. Vanselow-Algan ◽  
S. R. Schmidt ◽  
M. Greven ◽  
C. Fiencke ◽  
L. Kutzbach ◽  
...  
Keyword(s):  
Greenhouse Gas ◽  
Carbon Sink ◽  
Plant Litter ◽  
Time Span ◽  
Initial Increase ◽  
Emission Rates ◽  
Ch4 Emissions ◽  
Long Time ◽  
Ch4 And N2o ◽  
Carbon Dioxide Co2

Abstract. Natural peatlands are important carbon sinks and sources of methane (CH4). In contrast, drained peatlands turn from a carbon sink to a carbon source and potentially emit nitrous oxide (N2O). Rewetting of peatlands thus potentially implies climate change mitigation. However, data about the time span that is needed for the re-establishment of the carbon sink function by restoration are scarce. We therefore investigated the annual greenhouse gas (GHG) balances of three differently vegetated sites of a bog ecosystem 30 years after rewetting. All three vegetation communities turned out to be sources of carbon dioxide (CO2) ranging between 0.6 ± 1.43 t CO2 ha−2 yr−1 (Sphagnum-dominated vegetation) and 3.09 ± 3.86 t CO2 ha−2 yr−1 (vegetation dominated by heath). While accounting for the different global warming potential (GWP) of CO2, CH4 and N2O, the annual GHG balance was calculated. Emissions ranged between 25 and 53 t CO2-eq ha−1 yr−1 and were dominated by large emissions of CH4 (22–51 t CO2-eq ha−1 yr−1), with highest rates found at purple moor grass (Molinia caerulea) stands. These are to our knowledge the highest CH4 emissions so far reported for bog ecosystems in temperate Europe. As the restored area was subject to large fluctuations in the water table, we assume that the high CH4 emission rates were caused by a combination of both the temporal inundation of the easily decomposable plant litter of purple moor grass and the plant-mediated transport through its tissues. In addition, as a result of the land use history, mixed soil material due to peat extraction and refilling can serve as an explanation. With regards to the long time span passed since rewetting, we note that the initial increase in CH4 emissions due to rewetting as described in the literature is not inevitably limited to a short-term period.

scholarly journals CH<sub>4</sub> and N<sub>2</sub>O dynamics in the boreal forest–mire ecotone

2015 ◽  
Vol 12 (2) ◽  
pp. 281-297 ◽  
Author(s):  
B. Tupek ◽  
K. Minkkinen ◽  
J. Pumpanen ◽  
T. Vesala ◽  
E. Nikinmaa
Keyword(s):  
Ground Water ◽  
N2o Emission ◽  
N2o Emissions ◽  
Summer Drought ◽  
Drought Period ◽  
Local Climate ◽  
N2o Fluxes ◽  
Ch4 And N2o ◽  
Water Saturated ◽  
Boreal Landscapes

Abstract. In spite of advances in greenhouse gas research, the spatiotemporal CH4 and N2O dynamics of boreal landscapes remain challenging, e.g., we need clarification of whether forest–mire transitions are occasional hotspots of landscape CH4 and N2O emissions during exceptionally high and low ground water level events. In our study, we tested the differences and drivers of CH4 and N2O dynamics of forest/mire types in field conditions along the soil moisture gradient of the forest–mire ecotone. Soils changed from Podzols to Histosols and ground water rose downslope from a depth of 10 m in upland sites to 0.1 m in mires. Yearly meteorological conditions changed from being exceptionally wet to typical and exceptionally dry for the local climate. The median fluxes measured with a static chamber technique varied from −51 to 586 μg m−2 h−1 for CH4 and from 0 to 6 μg m−2 h−1 for N2O between forest and mire types throughout the entire wet–dry period. In spite of the highly dynamic soil water fluctuations in carbon rich soils in forest–mire transitions, there were no large peak emissions in CH4 and N2O fluxes and the flux rates changed minimally between years. Methane uptake was significantly lower in poorly drained transitions than in the well-drained uplands. Water-saturated mires showed large CH4 emissions, which were reduced entirely during the exceptional summer drought period. Near-zero N2O fluxes did not differ significantly between the forest and mire types probably due to their low nitrification potential. When upscaling boreal landscapes, pristine forest–mire transitions should be regarded as CH4 sinks and minor N2O sources instead of CH4 and N2O emission hotspots.

scholarly journals Methane and nitrous oxide fluxes across an elevation gradient in the tropical Peruvian Andes

2014 ◽  
Vol 11 (8) ◽  
pp. 2325-2339 ◽  
Author(s):  
Y. A. Teh ◽  
T. Diem ◽  
S. Jones ◽  
L. P. Huaraca Quispe ◽  
E. Baggs ◽  
...  
Keyword(s):  
Elevation Gradient ◽  
Laboratory Data ◽  
Montane Forest ◽  
N2o Emissions ◽  
Ch4 Flux ◽  
Peruvian Andes ◽  
Modelling Studies ◽  
N2o Fluxes ◽  
Ch4 And N2o ◽  
Montane Grasslands

Abstract. Remote sensing and inverse modelling studies indicate that the tropics emit more CH4 and N2O than predicted by bottom-up emissions inventories, suggesting that terrestrial sources are stronger or more numerous than previously thought. Tropical uplands are a potentially large and important source of CH4 and N2O often overlooked by past empirical and modelling studies. To address this knowledge gap, we investigated spatial, temporal and environmental trends in soil CH4 and N2O fluxes across a long elevation gradient (600–3700 m a.s.l.) in the Kosñipata Valley, in the southern Peruvian Andes, that experiences seasonal fluctuations in rainfall. The aim of this work was to produce preliminary estimates of soil CH4 and N2O fluxes from representative habitats within this region, and to identify the proximate controls on soil CH4 and N2O dynamics. Area-weighted flux calculations indicated that ecosystems across this altitudinal gradient were both atmospheric sources and sinks of CH4 on an annual basis. Montane grasslands (3200–3700 m a.s.l.) were strong atmospheric sources, emitting 56.94 ± 7.81 kg CH4-C ha−1 yr−1. Upper montane forest (2200–3200 m a.s.l.) and lower montane forest (1200–2200 m a.s.l.) were net atmospheric sinks (−2.99 ± 0.29 and −2.34 ± 0.29 kg CH4-C ha−1 yr−1, respectively); while premontane forests (600–1200 m a.s.l.) fluctuated between source or sink depending on the season (wet season: 1.86 ± 1.50 kg CH4-C ha−1 yr−1; dry season: −1.17 ± 0.40 kg CH4-C ha−1 yr−1). Analysis of spatial, temporal and environmental trends in soil CH4 flux across the study site suggest that soil redox was a dominant control on net soil CH4 flux. Soil CH4 emissions were greatest from habitats, landforms and during times of year when soils were suboxic, and soil CH4 efflux was inversely correlated with soil O2 concentration (Spearman's ρ = −0.45, P < 0.0001) and positively correlated with water-filled pore space (Spearman's ρ = 0.63, P <0.0001). Ecosystems across the region were net atmospheric N2O sources. Soil N2O fluxes declined with increasing elevation; area-weighted flux calculations indicated that N2O emissions from premontane forest, lower montane forest, upper montane forest and montane grasslands averaged 2.23 ± 1.31, 1.68 ± 0.44, 0.44 ± 0.47 and 0.15 ± 1.10 kg N2O-N ha−1 yr−1, respectively. Soil N2O fluxes from premontane and lower montane forests exceeded prior model predictions for the region. Comprehensive investigation of field and laboratory data collected in this study suggest that soil N2O fluxes from this region were primarily driven by denitrification; that nitrate (NO3−) availability was the principal constraint on soil N2O fluxes; and that soil moisture and water-filled porosity played a secondary role in modulating N2O emissions. Any current and future changes in N management or anthropogenic N deposition may cause shifts in net soil N2O fluxes from these tropical montane ecosystems, further enhancing this emission source.

scholarly journals Gas chromatography and photoacoustic spectroscopy for the assessment of soil greenhouse gases emissions

2013 ◽  
Vol 43 (2) ◽  
pp. 262-269 ◽  
Author(s):  
Rodrigo da Silveira Nicoloso ◽  
Cimélio Bayer ◽  
Genuir Luis Denega ◽  
Paulo Armando Victória de Oliveira ◽  
Martha Mayumi Higarashi ◽  
...  
Keyword(s):  
Gas Chromatography ◽  
Greenhouse Gases ◽  
Photoacoustic Spectroscopy ◽  
Cropping Systems ◽  
Agricultural Practices ◽  
N2o Emissions ◽  
N2o Fluxes ◽  
Carbon Dioxide Co2 ◽  
Ghg Fluxes

Assessments of soil carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O) emissions are critical for determination of the agricultural practices' potential to mitigate global warming. This study evaluated the photoacoustic spectroscopy (PAS) for the assessment of soil greenhouse gases (GHG) fluxes in comparison to the standard gas chromatography (GC) method. Two long-term experiments with different tillage and cropping systems over a Paleudult were evaluated using static chambers. PAS measurements of CO2 and N2O concentrations showed good relationship and linearity (R2=0.98 and 0.94, respectively) with GC results. However, CH4 measurements were significantly affected by air sample moisture which interfered on CH4 detection by PAS. Overestimation of CO2 and N2O concentrations in air samples determined by PAS (14.6 and 18.7%, respectively) were also related to sampling moisture. CO2 and N2O fluxes showed good agreement between methods (R2=0.96 and 0.95, respectively), though PAS overestimated fluxes by 18.6 and 13.6% in relation to GC results, respectively. PAS showed good sensitivity and was able to detect CO2 and N2O fluxes as low as 332mg CO2 m-2 h-1 and 21µg N2O m-2 h-1. PAS analyzer should be detailed calibrated to reduce humidity interference on CO2, CH4 and N2O concentrations measurements avoiding overestimation or erroneous determination of soil GHG fluxes.

Effects of increasing organic nitrogen inputs on CO2, CH4, and N2O fluxes in a temperate grassland

2021 ◽  
Vol 268 ◽  
pp. 115822
Author(s):  
Jihui Chen ◽  
Yingjun Zhang ◽  
Yi Yang ◽  
Tingting Tao ◽  
Xiao Sun ◽  
...  
Keyword(s):  
Organic Nitrogen ◽  
Temperate Grassland ◽  
Nitrogen Inputs ◽  
N2o Fluxes ◽  
Ch4 And N2o

scholarly journals Methane and nitrous oxide fluxes from the tropical Andes

2013 ◽  
Vol 10 (11) ◽  
pp. 17397-17438 ◽  
Author(s):  
Y. A. Teh ◽  
T. Diem ◽  
S. Jones ◽  
L. P. Huaraca Quispe ◽  
E. Baggs ◽  
...  
Keyword(s):  
Elevation Gradient ◽  
Laboratory Data ◽  
Montane Forest ◽  
N2o Emissions ◽  
Wet Season ◽  
Ch4 Flux ◽  
Modelling Studies ◽  
N2o Fluxes ◽  
Ch4 And N2o ◽  
Montane Grasslands

Abstract. Remote sensing and inverse modelling studies indicate that the tropics emit more CH4 and N2O than predicted by bottom-up emissions inventories, suggesting that terrestrial sources are stronger or more numerous than previously thought. Tropical uplands are a potentially large and important source of CH4 and N2O often overlooked by past empirical and modelling studies. To address this knowledge gap, we investigated spatial, temporal and environmental trends in CH4 and N2O fluxes across a~long elevation gradient (600–3700 m a.s.l.) in the Kosñipata Valley, in the southern Peruvian Andes that experiences seasonal fluctuations in rainfall. The aim of this work was to produce preliminary estimates of CH4 and N2O fluxes from representative habitats within this region, and to identify the proximate controls on soil CH4 and N2O dynamics. Ecosystems across this altitudinal gradient were both atmospheric sources and sinks of CH4 on an annual basis. Montane grasslands (or, puna; 3200–3700 m a.s.l.) were strong atmospheric sources, emitting 56.94 ± 7.81kg CH4-C ha−1 yr−1. Upper montane forest (2200–3200 m a.s.l.) and lower montane forest (1200–2200 m a.s.l.) were net atmospheric sinks (−2.99 ± 0.29 kg CH4-C ha−1 yr−1 and −2.34 ± 0.29 kg CH4-C ha−1 yr−1, respectively); while premontane forests (600–1200 m a.s.l.) fluctuated between source or sink depending on the season (wet season: 1.86 ± 1.50 CH4-C ha−1 yr−1; dry season: −1.17 ± 0.40 CH4-C ha−1 yr−1). Analysis of spatial, temporal and environmental trends in CH4 flux across the study site suggest that soil redox was a dominant control on net CH4 flux. CH4 emissions were greatest from elevations, landforms and during times of year when soils were sub-oxic, and CH4 efflux was inversely correlated with soil O2 concentration (r2 = 0.82, F1, 125 = 588.41, P < 0.0001). Ecosystems across the region were net atmospheric N2O sources. N2O fluxes declined with increasing elevation; N2O emissions from premontane forest, lower montane forest, upper montane forest and montane grasslands averaged 2.23 ± 1.31 kg N2O-N ha−1 yr−1, 1.68 ± 0.44 kg N2O-N ha−1 yr−1, 0.44 ± 0.47 kg N2O-N ha−1 yr−1 and 0.15 ± 1.10 kg N2O-N ha−1 yr−1, respectively. N2O fluxes from premontane and lower montane forests exceeded prior model predictions for the region. Comprehensive investigation of field and laboratory data collected in this study suggest that N2O fluxes from this region were primarily driven by denitrification; that nitrate (NO3−) availability was the principal constraint on N2O fluxes; and that soil moisture and water-filled porosity played a secondary role in modulating N2O emissions. Any current and future changes in N management or anthropogenic N deposition may cause shifts in net N2O fluxes from these tropical montane ecosystems, further enhancing this emission source.

Sign in / Sign up

Export Citation Format

Share Document