scholarly journals Wet and Dry Deposition Flux of Major Inorganic Ions at a High-Altitude Site in Himalayan Region (India)

2020 ◽  
Author(s):  
Anshu Sharma
PLoS ONE ◽  
2016 ◽  
Vol 11 (7) ◽  
pp. e0158616 ◽  
Author(s):  
Lijuan Zhu ◽  
Jiakai Liu ◽  
Ling Cong ◽  
Wenmei Ma ◽  
Wu Ma ◽  
...  

2020 ◽  
Author(s):  
Athanasios Nenes ◽  
Maria Kanakidou ◽  
Spyros Pandis ◽  
Armistead Russell ◽  
Shaojie Song ◽  
...  

<p>Nitrogen oxides (NOx) and ammonia (NH<sub>3</sub>) from anthropogenic and biogenic emissions are central contributors to particulate matter (PM) concentrations worldwide. Ecosystem productivity can also be strongly modulated by the atmospheric deposition of this inorganic "reactive nitrogen" nutrient. The response of PM and nitrogen deposition to changes in the emissions of both compounds is typically studied on a case-by-case basis, owing in part to the complex thermodynamic interactions of these aerosol precursors with other PM constituents. In the absence of rain, much of the complexity of nitrogen deposition is driven by the large difference in dry deposition velocity when a nitrogen-containing molecule is in the gas or condensed phase.</p><p>Here we present a simple but thermodynamically consistent approach that expresses the chemical domains of sensitivity of aerosol particulate matter to NH<sub>3</sub> and HNO<sub>3</sub> availability in terms of aerosol pH and liquid water content. From our analysis, four policy-relevant regimes emerge in terms of sensitivity: i) NH<sub>3</sub>-sensitive, ii) HNO<sub>3</sub>-sensitive, iii) combined NH<sub>3</sub> and HNO<sub>3</sub> sensitive, and, iv) a domain where neither NH<sub>3</sub> and HNO<sub>3</sub> are important for PM levels (but only nonvolatile precursors such as NVCs and sulfate). When this framework is applied to ambient measurements or predictions of PM and gaseous precursors, the “chemical regime” of PM sensitivity to NH3 and HNO3 availability is directly determined. </p><p>The same framework is then extended to consider the impact of gas-to-particle partitioning, on the deposition velocity of NH<sub>3</sub> and HNO<sub>3</sub> individually, and combined affects the dry deposition of inorganic reactive nitrogen. Four regimes of deposition velocity emerge: i) HNO<sub>3</sub>-fast, NH<sub>3</sub>-slow, ii) HNO<sub>3</sub>-slow, NH<sub>3</sub>-fast, iii) HNO<sub>3</sub>-fast, NH<sub>3</sub>-fast, and, iv) HNO<sub>3</sub>-slow, NH<sub>3</sub>-slow. Conditions that favor strong partitioning of species to the aerosol phase strongly delay the deposition of reactive nitrogen species and promotes their accumulation in the boundary layer and potential for long-range transport. </p><p>The use of these regimes allows novel insights and is an important tool to evaluate chemical transport models. Most notably, we find that nitric acid displays considerable variability of dry deposition flux, with maximum deposition rates found in the Eastern US (close to gas-deposition rates) and minimum rates for North Europe and China. Strong reductions in deposition velocity lead to considerable accumulation of nitrate aerosol in the boundary layer –up to 10-fold increases in PM2.5 nitrate aerosol, eventually being an important contributor to high PM2.5 levels observed during haze episodes. With this new understanding, aerosol pH and associated liquid water content can be understood as control parameters that drive PM formation and dry deposition flux and arguably can catalyze the accumulation of aerosol precursors that cause intense haze events throughout the globe.</p>


2005 ◽  
Vol 39 (2) ◽  
pp. 329-335 ◽  
Author(s):  
Masahiro Utiyama ◽  
Tsutomu Fukuyama ◽  
Kazuhiko Sakamoto ◽  
Hidekazu Ishihara ◽  
Atsuyuki Sorimachi ◽  
...  

2015 ◽  
Vol 15 (2) ◽  
pp. 951-972 ◽  
Author(s):  
Y. P. Pan ◽  
Y. S. Wang

Abstract. Atmospheric deposition is considered to be a major process that removes pollutants from the atmosphere and an important source of nutrients and contaminants for ecosystems. Trace elements (TEs), especially toxic metals deposited on plants and into soil or water, can cause substantial damage to the environment and human health due to their transfer and accumulation in food chains. Despite public concerns, quantitative knowledge of metal deposition from the atmosphere to ecosystems remains scarce. To advance our understanding of the spatiotemporal variations in the magnitudes, pathways, compositions and impacts of atmospherically deposited TEs, precipitation (rain and snow) and dry-deposited particles were collected simultaneously at 10 sites in Northern China from December 2007 to November 2010. The measurements showed that the wet and dry depositions of TEs in the target areas were orders of magnitude higher than previous observations within and outside China, generating great concern over the potential risks. The spatial distribution of the total (wet plus dry) deposition flux was consistent with that of the dry deposition, with a significant decrease from industrial and urban areas to suburban, agricultural and rural sites, while the wet deposition exhibited less spatial variation. In addition, the seasonal variation of wet deposition was also different from that of dry deposition, although they were both governed by the precipitation and emission patterns. For the majority of TEs that exist as coarse particles, dry deposition dominated the total flux at each site. This was not the case for potassium, nickel, arsenic, lead, zinc, cadmium, selenium, silver and thallium, for which the relative importance between wet and dry deposition fluxes varied by site. Whether wet deposition is the major atmospheric cleansing mechanism for the TEs depends on the size distribution of the particles. We found that atmospheric inputs of copper, lead, zinc, cadmium, arsenic and selenium were of the same magnitude as their increases in the topsoil of agricultural systems. At a background forest site in Northern China, the total deposition flux of lead observed in this study (14.1 mg m−2 yr−1) was twice that of the critical load calculated for temperate forest ecosystems in Europe. These findings provide baseline data needed for future targeting policies to protect various ecosystems from long-term heavy metal input via atmospheric deposition.


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