Modelling and mapping long-term risks due to reactive nitrogen effects: An overview of LRTAP convention activities

2008 ◽  
Vol 154 (3) ◽  
pp. 482-487 ◽  
Author(s):  
T. Spranger ◽  
J.-P. Hettelingh ◽  
J. Slootweg ◽  
M. Posch
2020 ◽  
Author(s):  
Pascal Wintjen ◽  
Frederik Schrader ◽  
Martijn Schaap ◽  
Burkhard Beudert ◽  
Christian Brümmer

<p>Reactive nitrogen (N<sub>r</sub>) compounds comprise essential nutrients for plants. However, a large supply of nitrogen by fertilization through atmospheric deposition may be harmful for ecosystems such as peatlands and may lead to a loss of biodiversity, soil acidification and eutrophication. In addition, nitrogen compounds may cause adverse human health impacts. Large parts of N<sub>r</sub> emissions originate from anthropogenic activities.  Emission hotspots of ΣN<sub>r</sub>, i.e. the sum of all N<sub>r</sub> compounds, are related to crop production and livestock farming (mainly through ammonia, NH<sub>3</sub>) and fossil fuel combustion by transport and industry (mainly through nitrogen oxides, NO<sub>2 </sub>and NO). Such additional amount of N<sub>r</sub> will enhance its biosphere-atmosphere exchange, affect plant health and can influence its photosynthetic capacity. Therefore, it is necessary to thoroughly estimate the nitrogen exchange between biosphere and atmosphere.</p><p>For measuring the nitrogen mixing ratios a converter for reactive nitrogen (TRANC: Total Reactive Atmospheric Nitrogen Converter) was used. The TRANC converts all reactive nitrogen compounds, except for nitrous oxide (N<sub>2</sub>O), to nitric oxide (NO) and is coupled to a fast-response chemiluminescence detector (CLD). Due to a low detection limit and a response time of about 0.3s the TRANC-CLD system can be used for flux calculation based on the eddy covariance (EC) technique. Flux losses, which are related to the experimental setup, different response characteristics and the general high reactivity of most N gases and aerosols, occur in the high frequency range. We estimated damping factors of approximately 20% with an empirical cospectral approach.</p><p>For getting a reliable prediction of ΣN<sub>r</sub> fluxes through deposition models, long-term flux measurements offer the possibility to verify the nitrogen uptake capacity and to investigate exchange characteristics of ΣN<sub>r </sub>in different ecosystems.</p><p>In this study, we compare modelled dry deposition fluxes using the deposition module DEPAC (DEPosition of Acidifying Compounds) within the chemical transport model LOTOS-EUROS (LOng Term Ozone Simulation – EURopean Operational Smog) against ΣN<sub>r</sub> flux measurements of the TRANC-CLD for a remote mixed forest site with hardly any local anthropogenic emission sources. This procedure allows to determine the background load and the natural exchange characteristics of nitrogen under low atmospheric concentrations. Therefore, the broad-scale dry deposition predicted directly by LOTOS-EUROS was compared to site-specific modelling results obtained using measured meteorological input data as well as the directly measured ΣN<sub>r</sub> fluxes. In addition, the influence of land-use weighting in LOTOS-EUROS was examined. We further compare our results to ΣN<sub>r</sub> deposition estimates obtained with canopy budget techniques. Measured ΣN<sub>r</sub> dry deposition at the site was 4.5 kg N ha<sup>-</sup><sup>1</sup> yr<sup>-</sup><sup>1</sup>, in close agreement with modelled estimates using DEPAC with measured drivers (5.2 kg N ha<sup>-</sup><sup>1</sup> yr<sup>-</sup><sup>1</sup>) and as integrated in the chemical transport model LOTOS-EUROS (5.2 kg N ha<sup>-</sup><sup>1</sup> yr<sup>-</sup><sup>1</sup> to 6.9 kg N ha<sup>-</sup><sup>1</sup> yr<sup>-</sup><sup>1</sup> depending on the weighting of land-use classes).</p><p>Our study is the first one presenting 2.5 years flux measurements of ΣN<sub>r</sub> above a remote mixed forest. Further verifications of long-term flux measurements against deposition models are useful to improve them and result in better understanding of exchange processes of ΣN<sub>r</sub>.</p>


2011 ◽  
Vol 45 (32) ◽  
pp. 5853-5862 ◽  
Author(s):  
Antoni L. Zbieranowski ◽  
Julian Aherne

2017 ◽  
Vol 17 (16) ◽  
pp. 10071-10091 ◽  
Author(s):  
Jeffrey A. Geddes ◽  
Randall V. Martin

Abstract. Reactive nitrogen oxides (NOy) are a major constituent of the nitrogen deposited from the atmosphere, but observational constraints on their deposition are limited by poor or nonexistent measurement coverage in many parts of the world. Here we apply NO2 observations from multiple satellite instruments (GOME, SCIAMACHY, and GOME-2) to constrain the global deposition of NOy over the last 2 decades. We accomplish this by producing top-down estimates of NOx emissions from inverse modeling of satellite NO2 columns over 1996–2014, and including these emissions in the GEOS-Chem chemical transport model to simulate chemistry, transport, and deposition of NOy. Our estimates of long-term mean wet nitrate (NO3−) deposition are highly consistent with available measurements in North America, Europe, and East Asia combined (r =  0.83, normalized mean bias  = −7 %, N =  136). Likewise, our calculated trends in wet NO3− deposition are largely consistent with the measurements, with 129 of the 136 gridded model–data pairs sharing overlapping 95 % confidence intervals. We find that global mean NOy deposition over 1996–2014 is 56.0 Tg N yr−1, with a minimum in 2006 of 50.5 Tg N and a maximum in 2012 of 60.8 Tg N. Regional trends are large, with opposing signs in different parts of the world. Over 1996 to 2014, NOy deposition decreased by up to 60 % in eastern North America, doubled in regions of East Asia, and declined by 20 % in parts of western Europe. About 40 % of the global NOy deposition occurs over oceans, with deposition to the North Atlantic Ocean declining and deposition to the northwestern Pacific Ocean increasing. Using the residual between NOx emissions and NOy deposition over specific land regions, we investigate how NOx export via atmospheric transport has changed over the last 2 decades. Net export from the continental United States decreased substantially, from 2.9 Tg N yr−1 in 1996 to 1.5 Tg N yr−1 in 2014. Export from China more than tripled between 1996 and 2011 (from 1.0 to 3.5 Tg N yr−1), before a striking decline to 2.5 Tg N yr−1 by 2014. We find that declines in NOx export from some western European countries have counteracted increases in emissions from neighboring countries to the east. A sensitivity study indicates that simulated NOy deposition is robust to uncertainties in NH3 emissions with a few exceptions. Our novel long-term study provides timely context on the rapid redistribution of atmospheric nitrogen transport and subsequent deposition to ecosystems around the world.


2016 ◽  
Vol 103 ◽  
pp. 308-319 ◽  
Author(s):  
Arnab Bhowmik ◽  
Ann-Marie Fortuna ◽  
Larry J. Cihacek ◽  
Andy I. Bary ◽  
Craig G. Cogger

2013 ◽  
Vol 6 (4) ◽  
pp. 927-936 ◽  
Author(s):  
B. Tuzson ◽  
K. Zeyer ◽  
M. Steinbacher ◽  
J. B. McManus ◽  
D. D. Nelson ◽  
...  

Abstract. A quantum cascade laser based absorption spectrometer for continuous and direct measurements of NO and NO2 was employed at the high-altitude monitoring site Jungfraujoch (3580 m a.s.l., Switzerland) during a three-month campaign in spring/summer 2012. The total reactive nitrogen, NOy, was also measured in the form of NO after conversion on a gold catalyst. The aim was to assess the suitability of the instrument for long-term monitoring of the main reactive nitrogen species under predominantly free tropospheric air conditions. A precision (1σ) of 10 and 3 ppt for NO and NO2 was achieved under field conditions after 180 s averaging time. The linear dynamic range of the instrument has been verified for both species from the detection limit up to 45 ppb. The spectrometer shared a common sampling inlet with a chemiluminescence-based analyzer. The comparison of the time series shows excellent agreement between the two techniques and demonstrates the adequacy of the laser spectroscopic approach for this kind of demanding environmental applications.


2012 ◽  
Vol 5 (6) ◽  
pp. 8969-8993 ◽  
Author(s):  
B. Tuzson ◽  
K. Zeyer ◽  
M. Steinbacher ◽  
J. B. McManus ◽  
D. D. Nelson ◽  
...  

Abstract. A quantum cascade laser based absorption spectrometer for continuous and direct measurements of NO and NO2 was employed at the high-altitude monitoring site Jungfraujoch (3580 m a.s.l., Switzerland) during a three month campaign in Spring/Summer 2012. The total reactive nitrogen, NOy, was also measured in the form of NO after conversion on a gold catalyst. The aim was to assess the suitability of the instrument for long-term monitoring of the main reactive nitrogen species under predominantly free tropospheric air conditions. A precision (1σ) of 10 and 3 ppt for NO and NO2 was achieved with 180 s averaging time under field conditions. The linear dynamic range of the instrument has been verified for both species from the detection limit to ≈45 ppbv. The spectrometer shared a common sampling inlet with a chemiluminescence-based analyzer. The comparison of the time series shows excellent agreement between the two techniques and demonstrates the adequacy of the laser spectroscopic approach for this kind of demanding environmental applications.


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