Sequential rainwater chemistry constrains in-cloud and below-cloud scavenging at a high-elevation site under contrasting transport regimes

Abstract. High-elevation receptors in monsoon Asia intercept cloud-bearing regional air, yet the event-scale transition from below-cloud removal to a cloud-dominated precipitation signature remains poorly constrained. We collected 203 sequential rainwater fractions from 55 precipitation events in 2023 at the Atmospheric Boundary Layer Eco-Environment Shanghuang Observatory (ABLES; 1128 m a.s.l.) in southeastern China, where complex terrain and frequent cloud occurrence expose the site to contrasting continental and marine transport. Twelve events with at least six fractions were analysed using major-ion chemistry, two independent late-stage baseline estimates, backward trajectories, and reanalysis fields, with near-surface meteorological and turbulence observations available for R3–R6. Anthropogenic-type events began with the largest ionic loads and strongest early decreases, dominated by sulfate, nitrate, and ammonium. Marine-type events had lower but more variable concentrations, whereas calcium persisted relative to secondary inorganic ions in crustal-type events. Median estimated in-cloud contributions were 51.1 % for sulfate, 58.4 % for nitrate, and 49.2 % for ammonium, with event values exceeding 80 %. These fractions exceeded compiled urban medians but overlapped remote-environment ranges. Although not a direct cloud-water measurement, the 0.32 mg L−1 late-event sulfate baseline was one to two orders of magnitude below historical Chinese mountain cloud-water observations and reached the lower range of global mountain records, consistent with sulfur controls extending beyond surface air. By resolving source-dependent within-event transitions hidden by bulk sampling, this study establishes an event- and ion-specific observational benchmark for wet scavenging at an inland mountain receptor and clarifies how continental–marine transport conditions the precipitation signature.

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Publication Details

Published
2026-11-06
DOI
https://doi.org/10.5194/egusphere-2026-6335
Primary Topic
Atmospheric chemistry and aerosols
Type
preprint

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preprint

Sequential rainwater chemistry constrains in-cloud and below-cloud scavenging at a high-elevation site under contrasting transport regimes

Baozhu Ge, Lingkai Dong, Yele Sun, Feili Li et al.
1 links
Atmospheric chemistry and aerosols
preprint

Sequential rainwater chemistry constrains in-cloud and below-cloud scavenging at a high-elevation site under contrasting transport regimes

Baozhu Ge, Lingkai Dong, Yele Sun, Feili Li, Xiaole Pan, Lanzhong Liu, Liquan Yao, YUCHENG CHEN, Jinyuan Xin, Xueling Cheng, Nuohang Liu, Zifa Wang
preprint en

Abstract

Abstract. High-elevation receptors in monsoon Asia intercept cloud-bearing regional air, yet the event-scale transition from below-cloud removal to a cloud-dominated precipitation signature remains poorly constrained. We collected 203 sequential rainwater fractions from 55 precipitation events in 2023 at the Atmospheric Boundary Layer Eco-Environment Shanghuang Observatory (ABLES; 1128 m a.s.l.) in southeastern China, where complex terrain and frequent cloud occurrence expose the site to contrasting continental and marine transport. Twelve events with at least six fractions were analysed using major-ion chemistry, two independent late-stage baseline estimates, backward trajectories, and reanalysis fields, with near-surface meteorological and turbulence observations available for R3–R6. Anthropogenic-type events began with the largest ionic loads and strongest early decreases, dominated by sulfate, nitrate, and ammonium. Marine-type events had lower but more variable concentrations, whereas calcium persisted relative to secondary inorganic ions in crustal-type events. Median estimated in-cloud contributions were 51.1 % for sulfate, 58.4 % for nitrate, and 49.2 % for ammonium, with event values exceeding 80 %. These fractions exceeded compiled urban medians but overlapped remote-environment ranges. Although not a direct cloud-water measurement, the 0.32 mg L−1 late-event sulfate baseline was one to two orders of magnitude below historical Chinese mountain cloud-water observations and reached the lower range of global mountain records, consistent with sulfur controls extending beyond surface air. By resolving source-dependent within-event transitions hidden by bulk sampling, this study establishes an event- and ion-specific observational benchmark for wet scavenging at an inland mountain receptor and clarifies how continental–marine transport conditions the precipitation signature.

Chinese Academy of Sciences (CN), Institute of Atmospheric Physics (CN), Henan Institute of Science and Technology (CN), University of Chinese Academy of Sciences (CN), Zhejiang University of Technology (CN)
National Natural Science Foundation of China, European Centre for Medium-Range Weather Forecasts
Clean water and sanitation, Climate action
Atmospheric chemistry and aerosols
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