scholarly journals Nitrogen oxides emission from two beech forests subjected to different nitrogen loads

2006 ◽  
Vol 3 (3) ◽  
pp. 293-310 ◽  
Author(s):  
B. Kitzler ◽  
S. Zechmeister-Boltenstern ◽  
C. Holtermann ◽  
U. Skiba ◽  
K. Butterbach-Bahl

Abstract. We analysed nitrogen oxides (N2O, NO) and carbon dioxide (CO2) emissions from two beech forest soils close to Vienna, Austria, which were exposed to different nitrogen input from the atmosphere. The site Schottenwald (SW) received 20.2 kg N ha−1 y−1 and Klausenleopoldsdorf (KL) 12.6 kg N ha−1 y−1 through wet deposition. Nitric oxide emissions from soil were measured hourly with an automatic dynamic chamber system. Daily N2O measurements were carried out by an automatic gas sampling system. Measurements of nitrous oxide (N2O) and CO2 emissions were conducted over larger areas on a biweekly (SW) or monthly (KL) basis by manually operated chambers. We used an autoregression procedure (time-series analysis) for establishing time-lagged relationships between N-oxides emissions and different climate, soil chemistry and N-deposition data. It was found that changes in soil moisture and soil temperature significantly effected CO2 and N-oxides emissions with a time lag of up to two weeks and could explain up to 95% of the temporal variations of gas emissions. Event emissions after rain or during freezing and thawing cycles contributed significantly (for NO 50%) to overall N-oxides emissions. In the two-year period of analysis the annual gaseous N2O emissions at SW ranged from 0.64 to 0.79 kg N ha−1 y−1 and NO emissions were 0.24 to 0.49 kg N ha−1 per vegetation period. In KL significantly lower annual N2O emissions (0.52 to 0.65 kg N2O-N kg ha−1 y−1) as well as considerably lower NO-emissions were observed. During a three-month measurement campaign NO emissions at KL were 0.02 kg N ha−1), whereas in the same time period significantly more NO was emitted in SW (0.32 kg NO-N ha−1). Higher N-oxides emissions, especially NO emissions from the high N-input site (SW) may indicate that atmospheric deposition has an impact on emissions of gaseous N from our forest soils. At KL there was a strong correlation between N-deposition and N-emission over time, which shows that low N-input sites are especially responsive to increasing N-inputs.

2005 ◽  
Vol 2 (5) ◽  
pp. 1381-1422 ◽  
Author(s):  
B. Kitzler ◽  
S. Zechmeister-Boltenstern ◽  
C. Holtermann ◽  
U. Skiba ◽  
K. Butterbach-Bahl

Abstract. We analysed nitrogen oxides (N2O, NO and NO2) and carbon dioxide (CO2) emissions from two beech forest soils close to Vienna, Austria, which were exposed to different nitrogen input from the atmosphere. The site Schottenwald (SW) received 22.6 kg N y-1 and Klausenleopoldsdorf (KL) 13.5 kg N y-1 through wet and dry deposition. Nitrogen oxide emissions from soil were measured hourly with an automatic dynamic chamber system. Daily N2O measurements were carried out by an automatic gas sampling system. Measurements of nitrous oxide (N2O) and CO2 emissions were conducted over larger areas on a biweekly (SW) or monthly (KL) basis by manually operated chambers. We used an autoregression procedure (time-series analysis) for establishing time-lagged relationships between N-oxide emissions and different climate, soil chemistry and N-deposition data. It was found that changes in soil moisture and soil temperature significantly effected CO2 and N-oxide emissions with a time lag of up to two weeks and could explain up to 95% of the temporal variations of gas emissions. Event emissions after rain or during freezing and thawing cycles contributed significantly (for NO 50%) to overall N-oxides emissions. In the two-year period of analysis the annual gaseous N2O losses at SW ranged from 0.65 to 0.77 kg N ha-1 y-1 and NO losses were 0.18 to 0.67 kg N ha-1 per vegetation period. In KL significantly lower annual N2O emissions (0.52 kg N2O-N kg ha-1 y-1) as well as considerably lower NO-losses were observed. During a three-month measurement campaign NO losses at KL were 0.02 kg, whereas in the same time period significantly more NO was emitted in SW (0.32 kg NO-N ha-1). Higher N-oxide emissions, especially NO emissions from the high N-input site (SW) indicate that atmospheric deposition had a strong impact on losses of gaseous N from our forest soils. At KL there was a strong correlation between N-deposition and N-emission over time, which shows that low N-input sites are especially responsive to increasing N-inputs.


2005 ◽  
Vol 2 (5) ◽  
pp. 1423-1455 ◽  
Author(s):  
B. Kitzler ◽  
S. Zechmeister-Boltenstern ◽  
C. Holtermann ◽  
U. Skiba ◽  
K. Butterbach-Bahl

Abstract. We measured nitrogen oxides (N2O and NOx), dinitrogen (N2) and carbon dioxide (CO2) emissions from a spruce-fir-beech forest soil in the North Tyrolean limestone Alps in Austria. The site received 12.1 kg nitrogen via wet and dry deposition. Fluxes of nitric oxide (NO) were measured by an automatic dynamic chamber system on an hourly basis over a two year period. Daily N2O emissions were obtained by a semi-automatic gas measuring system. In order to cover spatial variability biweekly manual measurements of N2O and CO2 emissions were carried out, additionally. For acquiring information on the effects of soil and meteorological conditions and of N-deposition on N-emissions we chose the autoregression procedure (time-series analysis) as our means of investigation. Hence, we could exclude the data's autocorrelation in the course of the time. We found that soil temperature, soil moisture and wet N-deposition followed by air temperature and precipitation were the most powerful influencing parameters effecting N-emissions. With these variables up to 89% of observed temporal variations of N-emissions could be explained. During the two-year investigation period between 2.5 and 3.5% of deposited N was reemitted in form of N2O whereas only 0.2% were emitted as NO. At our mountain forest site the main end-product of microbial activity processes was N2 and trace gases (N2O and NO) were only of minor importance.


2020 ◽  
Vol 56 (7) ◽  
pp. 1077-1090 ◽  
Author(s):  
Ling Song ◽  
Julia Drewer ◽  
Bo Zhu ◽  
Minghua Zhou ◽  
Nicholas Cowan ◽  
...  

Abstract Agricultural and forest soils with low organic C content and high alkalinity were studied over 17 days to investigate the potential response of the atmospheric pollutant nitric oxide (NO) and the greenhouse gas nitrous oxide (N2O) on (1) increased N deposition rates to forest soil; (2) different fertilizer types to agricultural soil and (3) a simulated rain event to forest and agricultural soils. Cumulative forest soil NO emissions (148–350 ng NO-N g−1) were ~ 4 times larger than N2O emissions (37–69 ng N2O-N g−1). Contrary, agricultural soil NO emissions (21–376 ng NO-N g−1) were ~ 16 times smaller than N2O emissions (45–8491 ng N2O-N g−1). Increasing N deposition rates 10 fold to 30 kg N ha−1 yr−1, doubled soil NO emissions and NO3− concentrations. As such high N deposition rates are not atypical in China, more attention should be paid on forest soil NO research. Comparing the fertilizers urea, ammonium nitrate, and urea coated with the urease inhibitor ‘Agrotain®,’ demonstrated that the inhibitor significantly reduced NO and N2O emissions. This is an unintended, not well-known benefit, because the primary function of Agrotain® is to reduce emissions of the atmospheric pollutant ammonia. Simulating a climate change event, a large rainfall after drought, increased soil NO and N2O emissions from both agricultural and forest soils. Such pulses of emissions can contribute significantly to annual NO and N2O emissions, but currently do not receive adequate attention amongst the measurement and modeling communities.


2005 ◽  
Vol 2 (4) ◽  
pp. 779-827 ◽  
Author(s):  
M. Kesik ◽  
P. Ambus ◽  
R. Baritz ◽  
N. Brüggemann ◽  
K. Butterbach-Bahl ◽  
...  

Abstract. Forest soils are a significant source for the primary and secondary greenhouse gases N2O and NO. However, current estimates are still uncertain due to the still limited number of field measurements and the herein observed pronounced variability of N trace gas fluxes in space and time, which are due to the variation of environmental factors such as soil and vegetation properties or meteorological conditions. To overcome these problems we further developed a process-oriented model, the PnET-N-DNDC model, which simulates the N trace gas exchange on the basis of the processes involved in production, consumption and emission of N trace gases. This model was validated against field observations of N trace gas fluxes from 19 sites obtained within the EU project NOFRETETE, and shown to perform well for N2O (r=0.68, slope=0.76) and NO (r2=0.78, slope=0.73). For the calculation of a European-wide emission inventory we linked the model to a detailed, regionally and temporally resolved database, comprising climatic properties (daily resolution), and soil parameters, and information on forest areas and types for the years 1990, 1995 and 2000. Our calculations show that N trace gas fluxes from forest soils may vary substantial from year to year and that distinct regional patterns can be observed. Our central estimate of NO emissions from forest soils in the EU amounts to 98.4, 84.9 and 99.2 kt N yr-1, using meteorology from 1990, 1995 and year 2000, respectively. This is <1.0% of pyrogenic NOx emissions. For N2O emissions the central estimates were 86.8, 77.6 and 81.6 kt N yr-1, respectively, which is approx. 14.5% of the source strength coming from agricultural soils. An extensive sensitivity analysis was conducted which showed a range in NO emissions from 44.4 to 254.0 kt N yr-1 for NO and 50.7 to 96.9 kt N yr-1 for N2O, for year 2000 meteorology. The results show that process-oriented models coupled to a GIS are useful tools for the calculation of regional, national, or global inventories of biogenic N-trace gas emissions from soils. This work represents the most comprehensive effort to date to simulate NO and N2O emissions from European forest soils.


2005 ◽  
Vol 2 (4) ◽  
pp. 353-375 ◽  
Author(s):  
M. Kesik ◽  
P. Ambus ◽  
R. Baritz ◽  
N. Brüggemann ◽  
K. Butterbach-Bahl ◽  
...  

Abstract. Forest soils are a significant source for the primary and secondary greenhouse gases N2O and NO. However, current estimates are still uncertain due to the still limited number of field measurements and the herein observed pronounced variability of N trace gas fluxes in space and time, which are due to the variation of environmental factors such as soil and vegetation properties or meteorological conditions. To overcome these problems we further developed a process-oriented model, the PnET-N-DNDC model, which simulates the N trace gas exchange on the basis of the processes involved in production, consumption and emission of N trace gases. This model was validated against field observations of N trace gas fluxes from 19 sites obtained within the EU project NOFRETETE, and shown to perform well for N2O (r2=0.68, slope=0.76) and NO (r2=0.78, slope=0.73). For the calculation of a European-wide emission inventory we linked the model to a detailed, regionally and temporally resolved database, comprising climatic properties (daily resolution), and soil parameters, and information on forest areas and types for the years 1990, 1995 and 2000. Our calculations show that N trace gas fluxes from forest soils may vary substantial from year to year and that distinct regional patterns can be observed. Our central estimate of NO emissions from forest soils in the EU amounts to 98.4, 84.9 and 99.2 kt N yr−1, using meteorology from 1990, 1995 and year 2000, respectively. This is <1.0% of pyrogenic NOx emissions. For N2O emissions the central estimates were 86.8, 77.6 and 81.6 kt N yr−1, respectively, which is approx. 14.5% of the source strength coming from agricultural soils. An extensive sensitivity analysis was conducted which showed a range in emissions from 44.4 to 254.0 kt N yr−1 for NO and 50.7 to 96.9 kt N yr−1 for N2O, for year 2000 meteorology. The results show that process-oriented models coupled to a GIS are useful tools for the calculation of regional, national, or global inventories of biogenic N trace gas emissions from soils. This work represents the most comprehensive effort to date to simulate NO and N2O emissions from European forest soils.


2006 ◽  
Vol 3 (4) ◽  
pp. 383-395 ◽  
Author(s):  
B. Kitzler ◽  
S. Zechmeister-Boltenstern ◽  
C. Holtermann ◽  
U. Skiba ◽  
K. Butterbach-Bahl

Abstract. We measured nitrogen oxides (N2O and NOx), dinitrogen (N2) and carbon dioxide (CO2) emissions from a spruce-fir-beech forest soil in the North Tyrolean limestone Alps in Austria. The site received 10.6–11.9 kg N ha−1 y−1 nitrogen as bulk deposition. Fluxes of nitric oxide (NO) were measured by an automatic dynamic chamber system on an hourly basis over a two year period. Daily N2O emissions were obtained by a semi-automatic gas measuring system. In order to cover spatial variability biweekly manual measurements of N2O and CO2 emissions were carried out in addition. For acquiring information on the effects of soil and meteorological conditions and of N-deposition on N-emissions we chose the auto-regression procedure (time-series analysis) as our means of investigation. Hence, we could exclude the data's autocorrelation in the course of the time. We found that soil temperature, soil moisture and bulk N-deposition followed by air temperature and precipitation were the most powerful influencing parameters effecting N-emissions. With these variables, up to 89% of observed temporal variations of N-emissions could be explained. During the two-year investigation period between 2.5 and 3.5% of deposited N was reemitted in form of N2O whereas only 0.2% were emitted as NO. At our mountain forest site the main end-product of microbial activity processes was N2 and trace gases (N2O and NO) were only of minor importance.


2005 ◽  
Vol 2 (4) ◽  
pp. 977-995 ◽  
Author(s):  
U. Skiba ◽  
J. Dick ◽  
R. Storeton-West ◽  
S. Fernades-Lopez ◽  
C. Wood ◽  
...  

Abstract. Intensive livestock farms emit large concentrations of NH3, most of which is deposited very close to the source. The presence of trees enhances the deposition. Rates to down wind forests can exceed 40 kg N ha-1. The steep gradient in large NH3 concentration and deposition at the edge of a downwind forest to background concentrations within a few hundred meters provides an ideal site to study the effect of different rates of N deposition on biological and chemical processes under similar environmental conditions. We have investigated the effect of different rates of NH3 deposition (62, 45, 24 and 5 kg NH3-N ha-1 y-1) on the flux of NO and N2O from soil in a mixed woodland downwind of a large poultry farm (160000 birds) in Scotland, which has been operating for about 40 years. Measurements were carried out for a 6 month period, with hourly NO flux measurements, daily N2O fluxes close to the farm and monthly at all sites and monthly cumulative wet and dry N deposition. The increased NH3 and NH4+ deposition to the woodland increased emissions of NO and N2O and soil available NH4+ and NO3- concentrations. Average NO and N2O fluxes measured 15, 25 and 45 m downwind of the farm were 111.2±41.1, 123.3±40.7, 38.3±28.8 µg NO-N m-2 h-1 and 9.9±7.5, 34.3±33.3 and 21.2±6.1 µg NO-N m-2 h-1, respectively. At the background site 270 m downwind the N2O flux was reduced to 1.75±2.1 µg N2O-N m-2 h-1. NO emissions were significantly influenced by seasonal and daily changes in soil temperature and followed a diurnal pattern with maximum emissions approximately 3h after noon. For N2O no consistent diurnal pattern was observed. Changes in soil moisture content had a less clear effect on the NO and N2O flux. On average the NO emissions expressed as a fraction of the elevated N deposited were 7.1% (at 15 m), 6% (at 25 m) and 2.3% (at 45 m) downwind of the farm, whereas for N2O the emissions were only 2.8% (at 15 m), 3% (at 25 m) and 3% (at 45 m) downwind. These emission fractions exceed the emission factor of 1% advised by the IPCC for N2O emissions resulting from atmospheric N deposition.


2021 ◽  
Vol 304-305 ◽  
pp. 108434
Author(s):  
Yujie Shi ◽  
Junfeng Wang ◽  
Ya'nan Li ◽  
Jinwei Zhang ◽  
Yunna Ao ◽  
...  
Keyword(s):  

Agronomy ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 1477
Author(s):  
Antonio Marín-Martínez ◽  
Alberto Sanz-Cobeña ◽  
Mª Angeles Bustamante ◽  
Enrique Agulló ◽  
Concepción Paredes

In semi-arid vineyard agroecosystems, highly vulnerable in the context of climate change, the soil organic matter (OM) content is crucial to the improvement of soil fertility and grape productivity. The impact of OM, from compost and animal manure, on soil properties (e.g., pH, oxidisable organic C, organic N, NH4+-N and NO3−-N), grape yield and direct greenhouse gas (GHG) emission in vineyards was assessed. For this purpose, two wine grape varieties were chosen and managed differently: with a rain-fed non-trellising vineyard of Monastrell, a drip-irrigated trellising vineyard of Monastrell and a drip-irrigated trellising vineyard of Cabernet Sauvignon. The studied fertiliser treatments were without organic amendments (C), sheep/goat manure (SGM) and distillery organic waste compost (DC). The SGM and DC treatments were applied at a rate of 4600 kg ha−1 (fresh weight, FW) and 5000 kg ha−1 FW, respectively. The use of organic amendments improved soil fertility and grape yield, especially in the drip-irrigated trellising vineyards. Increased CO2 emissions were coincident with higher grape yields and manure application (maximum CO2 emissions = 1518 mg C-CO2 m−2 d−1). In contrast, N2O emissions, mainly produced through nitrification, were decreased in the plots showing higher grape production (minimum N2O emissions = −0.090 mg N2O-N m−2 d−1). In all plots, the CH4 fluxes were negative during most of the experiment (−1.073−0.403 mg CH4-C m−2 d−1), indicating that these ecosystems can represent a significant sink for atmospheric CH4. According to our results, the optimal vineyard management, considering soil properties, yield and GHG mitigation together, was the use of compost in a drip-irrigated trellising vineyard with the grape variety Monastrell.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Quan Li ◽  
Changhui Peng ◽  
Junbo Zhang ◽  
Yongfu Li ◽  
Xinzhang Song

AbstractForest soils play an important role in controlling global warming by reducing atmospheric methane (CH4) concentrations. However, little attention has been paid to how nitrogen (N) deposition may alter microorganism communities that are related to the CH4 cycle or CH4 oxidation in subtropical forest soils. We investigated the effects of N addition (0, 30, 60, or 90 kg N ha−1 yr−1) on soil CH4 flux and methanotroph and methanogen abundance, diversity, and community structure in a Moso bamboo (Phyllostachys edulis) forest in subtropical China. N addition significantly increased methanogen abundance but reduced both methanotroph and methanogen diversity. Methanotroph and methanogen community structures under the N deposition treatments were significantly different from those of the control. In N deposition treatments, the relative abundance of Methanoculleus was significantly lower than that in the control. Soil pH was the key factor regulating the changes in methanotroph and methanogen diversity and community structure. The CH4 emission rate increased with N addition and was negatively correlated with both methanotroph and methanogen diversity but positively correlated with methanogen abundance. Overall, our results suggested that N deposition can suppress CH4 uptake by altering methanotroph and methanogen abundance, diversity, and community structure in subtropical Moso bamboo forest soils.


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