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Reactive nitrogen (Nr) plays a key role in the atmospheric environment and its deposition has induced large negative impacts on ecosystem health and services. Five-year continuous in-situ monitoring of N deposition, including wet (total nitrogen ( W TN), total dissolved nitrogen ( W TDN), dissolved organic nitrogen ( W DON), ammonium nitrogen ( W AN) and nitrate nitrogen ( W NN)) and dry ( D NH 3 , D HNO 3 , D pNH 4 + , D pNO 3 − and D NO 2 ) deposition, had been conducted since August 2008 to December 2013 (wet) and May 2011 to December 2013 (dry) in Yan-ting, China, a typical agricultural area in the central Sichuan Basin. Mean annual total N deposition from 2011 to 2013 was 30.8 kg N ha −1 yr −1 , and speculated that of 2009 and 2010 was averaged 28.2 kg N ha −1 yr −1 , respectively. Wet and dry N deposition accounted for 76.3% and 23.7% of annual N deposition, respectively. Reduced N ( W AN, D NH 3 and D pNH 4 + ) was 1.7 times of oxidized N ( W NN, D HNO 3 , D NO 2 and D pNO 3 − ) which accounted for 50.9% and 30.3% of TN, respectively. Maximum loadings of all N forms of wet deposition, gaseous NH 3 , HNO 3 and particulate NH 4 + in dry deposition occurred in summer and minimum loadings in winter. Whether monthly, seasonal or annual averaged, dissolved N accounted for more than 70% of the total. N deposition in the central Sichuan Basin increased during the sampling period, especially that of ammonium compounds, and has become a serious threat to local aquatic ecosystems, the surrounding forest and other natural or semi-natural ecosystems in the upper reaches of the Yangtze River. [ABSTRACT FROM AUTHOR]

Atmospheric nitrogen (N) deposition plays an important role in the global N cycle. Data for dry and wet N deposition in agricultural ecosystem of Shaanxi in China is still imperfect; in this study, we continuously measured concentrations and fluxes of dry N deposition from 2010 to 2013 in Yangling district of Shaanxi province and wet N deposition from 2010 to 2012. The average annual concentrations of NH, NO, HNO, particulate ammonium, and nitrate (pNH and pNO) varied among 3.9-9.1, 6.6-8.0, 1.2-1.4, 3.1-4.3, and 3.3-4.8 μg N m, respectively, with mean values of 6.0, 7.2, 1.3, 3.8, and 4.1 μg N m, respectively, during the entire monitoring period. The annual NH-N and NO-N concentrations in precipitation ranged 3.9-4.3 and 2.8-3.4 mg N L with the mean values of 4.1 and 3.3 mg N L. The NH-N/NO-N ratio in rainfall averaged 1.2. Dry N deposition flux was determined to be 19.2 kg N ha year and the wet N deposition flux was 27.2 kg N ha year. The amount of total atmospheric N deposition (dry plus wet) reached 46.4 kg N ha year, in which dry deposition accounted 41 %. Gaseous N deposition comprised over 75 % of the dry deposition, and the proportion of oxidized N in dry deposition was equal to the reduced N. Therefore, the results suggest that more stringent regional air pollution control policies are required in the target area and that N deposition is an important nutrient resource from the atmosphere that must be taken into consideration in nutrient management planning of agricultural ecosystems. [ABSTRACT FROM AUTHOR]

The study of emissions and depositions of atmospheric reactive nitrogen species (N r s) in a region is important to uncover the sources and sinks of atmospheric N r s in the region. In this study, atmospheric total N r s depositions including both wet-only and dry deposition were monitored simultaneously across major land-use types in a 105 km2 catchment called Jinjing River Catchment (JRC) in subtropical central China from 2015 to 2016. Based on activity data and emission factors for the main N r s emission sources, ammonia (NH 3) and nitrogen oxides (NO x) emission inventories for the catchment were also compiled. The estimated total N r s deposition in JRC was 35.9 kg N ha−1 yr−1, with approximately 49.7 % attributed to reduced compounds (NH x), and 40.5 % attributed to oxidized (NO y). The total N r s emission rate in JRC was 80.4 kg N ha−1 yr−1, with 61.5 and 18.9 kg N ha−1 yr−1 from NH 3 and NO x emissions, respectively. Livestock excretion and fertilization were the two main contributing emission sources for NH 3 , while vehicle sources contributed the bulk of NO x emissions. The net atmospheric budgets of N r s in paddy field, forest, and tea field were +3.7, −36.1, and +23.8 kg N ha−1 yr−1, respectively. At the catchment scale, the net atmospheric budget of N r s was +47.7 kg N ha−1 yr−1, with +43.7 kg N ha−1 yr−1 of NH x and +4.0 kg N ha−1 yr−1 of NO y , indicating that the subtropical catchment was net sources of atmospheric N r s. Considering that excessive atmospheric N r emissions and deposition may cause adverse effects on the environment, effects should be conducted to mitigate the N r s emissions from agriculture and transportation, and increasing the area of forest is good for reducing the net positive budget of atmospheric N r s in the subtropical catchments in China. [Display omitted] • Mean atmospheric N r deposition was 36 kg N ha−1 yr−1 in a subtropical catchment in a 2-yr study. • Total N r emissions in catchment were 80 kg N ha−1 yr−1, with 62 kg N ha−1 yr−1 from NH 3 emissions. • The net N r budget showed high emissions due to NH 3 emissions from livestock and fertilization. • Paddy and tea fields were net sources of N r s, while forest was a net strong sink of N r s. Both atmospheric emissions and depositions of Nrs were high, and the net budget showed high emissions in a typical agricultural catchment in subtropical central China. [ABSTRACT FROM AUTHOR]

In a recent publication in the journal Science of the Total Environment, Zhu et al. (2015) reported the composition, spatial patterns, and factors influencing atmospheric wet nitrogen (N) deposition based on one year's data from 41-monitoring sites in China. We suspect their results may largely underestimate dissolved organic N (DON) but overestimate total particulate N (TPN) in wet deposition due to the uncertainty resulting from the sampling, storage and analysis methods in their study. Our suspicions are based mainly on our experience from earlier measurements and the literature. We therefore suggest that enhanced data quality control on atmospheric N deposition measurements should be taken into account in future studies. [ABSTRACT FROM AUTHOR]

In a publication in Atmospheric Environment ( http://dx.doi.org/10.1016/j.atmosenv.2015.10.081 ), Gu et al. (2015) estimated that “the total nitrogen (N) deposition in 2010 was 2.32 g N m −2 yr −1 ” in China. This value is comparable with previous estimations based on a synthesized dataset of wet/bulk inorganic N deposition observations, which underestimates the total N deposition since their algorithm (equations (2) and (3) in their paper) does not account for dry deposition of NH 3 , HNO 3 , NO x and wet/dry deposition of HONO and organic nitrogen (e.g. amines, amides, PAN). Indeed, Gu et al. (2015) mixed the terminology of wet/bulk deposition and total deposition. Another flawed assumption by Gu et al. (2015) is that all inorganic N in precipitation estimated by their algorithm originates from fertilizer and coal combustion. This is incorrect and almost certainly causes biases in the spatial and temporal distribution of estimated wet/bulk inorganic N deposition (Fig. 5 in their paper), further considering the fact that they neglected important N sources like livestock and they did not consider the nonlinearity between various sources and deposition. Besides the input data on N deposition, the model validation (Sect. 2.3.2) described in their paper also requires clarification because the detailed validation information about the time series of observational dataset versus modeling results was not given. As a result of these combined uncertainties in their estimation of N deposition and the lack of detail for model-measurement comparison, their estimates of the impacts of N deposition on carbon storage in Chinese forests may need further improvement. We suggest the clarification of the terminology regarding N deposition, especially for wet deposition, bulk deposition, gaseous and particulate dry deposition or total deposition since the accurate distinction between these terms is crucial to investigating and estimating the effects of N deposition on ecosystems. [ABSTRACT FROM AUTHOR]

Atmospheric nitrogen (N) deposition is currently high and meanwhile diffuse N pollution is also serious in China. The correlation between N deposition and riverine N export and the contribution of N deposition to riverine N export were investigated in a typical hilly red soil catchment in southern China over a two-year period. N deposition was as high as 26.1 to 55.8 kg N/(ha·yr) across different land uses in the studied catchment, while the riverine N exports ranged from 7.2 to 9.6 kg N/(ha·yr) in the forest sub-catchment and 27.4 to 30.3 kg N/(ha·yr) in the agricultural sub-catchment. The correlations between both wet N deposition and riverine N export and precipitation were highly positive, and so were the correlations between NH 4 + -N or NO 3 − -N wet deposition and riverine NH 4 + -N or NO 3 − -N exports except for NH 4 + -N in the agricultural sub-catchment, indicating that N deposition contributed to riverine N export. The monthly export coefficients of atmospheric deposited N from land to river in the forest sub-catchment (with a mean of 14%) presented a significant positive correlation with precipitation, while the monthly contributions of atmospheric deposition to riverine N export (with a mean of 18.7% in the agricultural sub-catchment and a mean of 21.0% in the whole catchment) were significantly and negatively correlated with precipitation. The relatively high contribution of N deposition to diffuse N pollution in the catchment suggests that efforts should be done to control anthropogenic reactive N emissions to the atmosphere in hilly red soil regions in southern China. [ABSTRACT FROM AUTHOR]