Dataset Information

A database of atmospheric nitrogen concentration and deposition from the nationwide monitoring network in China.

ABSTRACT: Atmospheric nitrogen (N) deposition has increased substantially across China since 1980; however, data for N deposition fluxes since the 2000s has been very limited. Understanding and mitigating the impacts of N deposition requires long-term quantification of dry as well as wet deposition of key reactive nitrogen (Nr) species. Here we present a dataset for inorganic N concentrations and deposition for the period 2010-2015 in China, compiled from the nationwide deposition monitoring network. The dataset comprises information from 32 monitoring sites on concentrations and bulk deposition (wet plus part of dry deposition) fluxes of NH4+-N and NO3--N, air concentrations and dry deposition fluxes of the major Nr species NH3, NO2, HNO3, and particulate NH4+ and NO3-. This unique database is available inter alia to advance understanding of the spatial patterns of inorganic N concentrations and deposition in China and its associated effects, constrain primary Nr (e.g., NH3, NOx) emission inventories, and validate outputs of atmospheric chemistry and transport models.

SUBMITTER: Xu W

PROVIDER: S-EPMC6509345 | biostudies-other | 2019 May

REPOSITORIES: biostudies-other

ACCESS DATA

Publications

A database of atmospheric nitrogen concentration and deposition from the nationwide monitoring network in China.

Xu Wen W Zhang Lin L Liu Xuejun X

Scientific data 20190509 1

Atmospheric nitrogen (N) deposition has increased substantially across China since 1980; however, data for N deposition fluxes since the 2000s has been very limited. Understanding and mitigating the impacts of N deposition requires long-term quantification of dry as well as wet deposition of key reactive nitrogen (Nr) species. Here we present a dataset for inorganic N concentrations and deposition for the period 2010-2015 in China, compiled from the nationwide deposition monitoring network. The ...[more]

PMID: 31073123

Similar Datasets

Project description:Size-segregated aerosol particles were collected using a high volume MOUDI sampler at a coastal urban site in Xiamen Bay, China, from March 2018 to June 2020 to examine the seasonal characteristics of aerosol and water-soluble inorganic ions (WSIIs) and the dry deposition of nitrogen species. During the study period, the annual average concentrations of PM1, PM2.5, PM10, and TSP were 14.8 ± 5.6, 21.1 ± 9.0, 35.4 ± 14.2 μg m-3, and 45.2 ± 21.3 μg m-3, respectively. The seasonal variations of aerosol concentrations were impacted by the monsoon with the lowest value in summer and the higher values in other seasons. For WSIIs, the annual average concentrations were 6.3 ± 3.3, 2.1 ± 1.2, 3.3 ± 1.5, and 1.6 ± 0.8 μg m-3 in PM1, PM1-2.5, PM2.5-10, and PM>10, respectively. In addition, pronounced seasonal variations of WSIIs in PM1 and PM1-2.5 were observed, with the highest concentration in spring-winter and the lowest in summer. The size distribution showed that SO4 2-, NH4 + and K+ were consistently present in the submicron particles while Ca2+, Mg2+, Na+ and Cl- mainly accumulated in the size range of 2.5-10 μm, reflecting their different dominant sources. In spring, fall and winter, a bimodal distribution of NO3 - was observed with one peak at 2.5-10 μm and another peak at 0.44-1 μm. In summer, however, the fine mode peak disappeared, likely due to the unfavorable conditions for the formation of NH4NO3. For NH4 + and SO4 2-, their dominant peak at 0.25-0.44 μm in summer and fall shifted to 0.44-1 μm in spring and winter. Although the concentration of NO3-N was lower than NH4-N, the dry deposition flux of NO3-N (35.77 ± 24.49 μmol N m-2 d-1) was much higher than that of NH4-N (10.95 ± 11.89 μmol N m-2 d-1), mainly due to the larger deposition velocities of NO3-N. The contribution of sea-salt particles to the total particulate inorganic N deposition was estimated to be 23.9-52.8%. Dry deposition of particulate inorganic N accounted for 0.95% of other terrestrial N influxes. The annual total N deposition can create a new productivity of 3.55 mgC m-2 d-1, accounting for 1.3-4.7% of the primary productivity in Xiamen Bay. In light of these results, atmospheric N deposition could have a significant influence on biogeochemistry cycle of nutrients with respect to projected increase of anthropogenic emissions from mobile sources in coastal region.Supplementary informationThe online version contains supplementary material available at 10.1007/s10874-021-09427-8.

Project description:The Chesapeake Bay watershed has been the focus of pioneering studies of the role of atmospheric nitrogen (N) deposition as a nutrient source and driver of estuarine trophic status. Here, we review the history and evolution of scientific investigations of the role of atmospheric N deposition, examine trends from wet and dry deposition networks, and present century-long (1950-2050) atmospheric N deposition estimates. Early investigations demonstrated the importance of atmospheric deposition as an N source to the Bay, providing 25%-40% among all major N sources. These early studies led to the unprecedented inclusion of targeted decreases in atmospheric N deposition as part of the multi-stakeholder effort to reduce N loads to the Bay. Emissions of nitrogen oxides (NOx) and deposition of wet nitrate, oxidized dry N, and dry ammonium (NH4+) sharply and synchronously declined by 60%-73% during 1995-2019. These decreases largely resulted from implementation of Title IV of the 1990 Clean Air Act Amendments, which began in 1995. Wet NH4+ deposition shows no significant trend during this period. The century-long atmospheric N deposition estimates indicate an increase in total atmospheric N deposition in the Chesapeake watershed from 1950 to a peak of ~15 kg N/ha/yr in 1979, trailed by a slight decline of <10% through the mid-1990s, and followed by a sharp decline of about 40% thereafter through 2019. An additional 21% decline in atmospheric N deposition is projected from 2015 to 2050. A comparison of the Potomac River and James River watersheds indicates higher atmospheric N deposition in the Potomac, likely resulting from greater emissions from higher proportions of agricultural and urban land in this basin. Atmospheric N deposition rose from 30% among all N sources to the Chesapeake Bay watershed in 1950 to a peak of 40% in 1973, and a decline to 28% by 2015. These data highlight the important role of atmospheric N deposition in the Chesapeake Bay watershed and present a potential opportunity for decreases in deposition to contribute to further reducing N loads and improving the trophic status of tidal waters.

Dataset Information

A database of atmospheric nitrogen concentration and deposition from the nationwide monitoring network in China.

Publications

A database of atmospheric nitrogen concentration and deposition from the nationwide monitoring network in China.

Similar Datasets

OmicsDI is part of the ELIXIR infrastructure

Tweets