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Investigating atmospheric nitrate sources and formation pathways between heating and non-heating seasons in urban North China
Abstract In urban North China, nitrate ( NO 3 − ) is a primary contributor to haze formation. So far, the production processes and source apportionments of atmospheric NO 3 − during the heating season (i.e. the wintertime) have not yet been well understood. This study determined δ 15 N– NO 3 − , δ 1...
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Published in: | Environmental research letters 2023-03, Vol.18 (3), p.34006 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Abstract
In urban North China, nitrate (
NO
3
−
) is a primary contributor to haze formation. So far, the production processes and source apportionments of atmospheric
NO
3
−
during the heating season (i.e. the wintertime) have not yet been well understood. This study determined δ
15
N–
NO
3
−
, δ
18
O–
NO
3
−
, and Δ
17
O–
NO
3
−
of aerosol samples to compare the potential sources and formation pathways of atmospheric
NO
3
−
during heating (November to March) and non-heating (April to May) seasons. Combining stable isotope composition with the MixSIAR model based on Δ
17
O–
NO
3
−
showed that NO
3
+ DMS/HC (dimethyl sulfate/hydrocarbon) pathway was the dominant process of atmospheric nitrate formation during the heating season (mean = 52.88 ± 16.11%). During the non-heating season, the contributions of NO
3
+ DMS/HC (mean = 37.89 ± 13.57%) and N
2
O
5
+ H
2
O (mean = 35.24 ± 3.75%) pathways were comparable. We found that Δ
17
O–
NO
3
−
was negatively correlated with wind speed and positively correlated with relative humidity during the heating season, possibly associated with the sources and production of atmospheric
NO
3
−
. In specific, in a dust storm event, the very low Δ
17
O–
NO
3
−
is likely associated with particles from land surface. Under the premise of considering
15
N fractionation, the constraint-based on δ
15
N–
NO
3
−
illustrated that coal combustion was the major source of NO
x
emission during the heating season, and the relative contribution of coal combustion decreased rapidly from the heating season (mean = 42.56 ± 15.50%) to the non-heating season (mean = 21.86 ± 4.91%). Conversely, the proportion of NO
x
emitted by soil microbes rose significantly from the heating (mean = 9.67 ± 5.99%) to non-heating season (mean = 24.02 ± 11.65%). This study revealed differences in the sources and formation processes of atmospheric
NO
3
−
during the heating and non-heating seasons, which are of significance to atmospheric nitrogen oxide/nitrate pollution mitigation. |
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ISSN: | 1748-9326 1748-9326 |
DOI: | 10.1088/1748-9326/acb805 |