| Autor: |
Xiawei Yu, Xiyuan Chi, Hui Kang, Zhouqing Xie, Haicong Zhan, Cheng Liu, Shidong Fan, Pengzhen He |
| Rok vydání: |
2018 |
| Předmět: |
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| Zdroj: |
Atmospheric Chemistry and Physics. 18:14465-14476 |
| ISSN: |
1680-7324 |
| DOI: |
10.5194/acp-18-14465-2018 |
| Popis: |
The rapid mass increase of atmospheric nitrate is a critical driving force for the occurrence of fine-particle pollution (referred to as haze hereafter) in Beijing. However, the exact mechanisms for this rapid increase of nitrate mass have not been well constrained from field observations. Here we present the first observations of the oxygen-17 excess of atmospheric nitrate ( Δ 17 O ( NO 3 - ) ) collected in Beijing haze to reveal the relative importance of different nitrate formation pathways, and we also present the simultaneously observed δ 15 N ( NO 3 - ) . During our sampling period, 12 h averaged mass concentrations of PM2.5 varied from 16 to 323 µ g m −3 with a mean of ( 141±88 (1SD)) µ g m −3 , with nitrate ranging from 0.3 to 106.7 µ g m −3 . The observed Δ 17 O ( NO 3 - ) ranged from 27.5 ‰ to 33.9 ‰ with a mean of ( 30.6±1.8 ) ‰, while δ 15 N ( NO 3 - ) ranged from −2.5 ‰ to 19.2 ‰ with a mean of ( 7.4±6.8 ) ‰. Δ 17 O ( NO 3 - ) -constrained calculations suggest nocturnal pathways ( N 2 O 5 + H 2 O / Cl - and NO3+HC ) dominated nitrate production during polluted days ( PM2.5≥75 µ g m −3 ), with a mean possible fraction of 56–97 %. Our results illustrate the potentiality of Δ17O in tracing nitrate formation pathways; future modeling work with the constraint of isotope data reported here may further improve our understanding of the nitrogen cycle during haze. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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