High-Time-Resolution Aerosol Chemistry and Machine-Learning Sensitivity Reveal a Highland Triad Mechanism Driving PM2.5 in Xining (Qinghai–Tibet Plateau)

Fine particulate matter (PM2.5) formation mechanisms in fragile highland ecosystems remain inadequately constrained, particularly regarding thermodynamic non-linearities (aerosol pH, liquid water content) and their interaction with geochemical modulation. Here, we present comprehensive year-long online measurements from Xining, Qinghai-Tibet Plateau, integrating hourly measurements of water-soluble ions, inorganic elements, and gaseous precursors with ISORROPIA-II thermodynamic modeling and ensemble machine learning. Median pH was 4.38 but exhibited two distinct pH regimes (14.8% pH < 3.0, 11.5% pH > 7.2), with acute acidification enhancing toxic metal solubility (Fe, Pb by 3-5×), and it posed distinct ecological risks. Our analysis reveals a distinct “highland mechanism triad” governing PM2.5 dynamics: (1) winter meteorological confinement amplifying dust-catalyzed sulfate formation (SOR = 0.68); (2) spring alkaline dust buffering (pH > 7.2) that titrates NH3 and suppresses nitrate formation (NOR < 0.10); and (3) summer photochemical oxidation constrained by chronic NH3 limitation within an oxidant-excess regime. Random Forest achieved optimal prediction for the chemically active inorganic fraction (RMSE = 6.63 μg/m3, R2 = 0.91) by learning regime-specific non-linearities, with local sensitivity analysis identifying Ca2+, SO42−, and Al as chemically sensitive drivers (S > 0.35) while revealing NH3’s seasonally variable influence (rank 15 in winter, significant in summer; S > 0.28), subsequently complemented by global SHAP analysis, which further revealed NO3− as the most robust predictor (ranking 1st–2nd) and captured NH3’s non-linear threshold effects (). Positive Matrix Factorization apportioned secondary aerosols (30.11%) within a unique alkaline–dust matrix. These findings demonstrate that highland PM2.5 inorganic chemistry operates through fundamentally different pathways than lowland photochemical haze, with acid-induced toxic metal activation providing a new target for ecological protection in this fragile ecosystem. Seasonally adaptive mitigation is required: concurrent SO2-NH3 control in winter, dust suppression infrastructure in spring, and agricultural NH3 capture in summer. This integrated framework provides a transferable methodology for air-quality management in alkaline dust-dominated, NH3-limited highland ecosystems (>2000 m).

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Journal
Atmosphere
Published
2026-02-13
DOI
https://doi.org/10.3390/atmos17020200
Primary Topic
Atmospheric chemistry and aerosols
Type
article
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article

High-Time-Resolution Aerosol Chemistry and Machine-Learning Sensitivity Reveal a Highland Triad Mechanism Driving PM2.5 in Xining (Qinghai–Tibet Plateau)

Weijun Song, Zihong Liang, Xiaofeng Hu, Guojuan Qu et al.
Atmosphere
Atmospheric chemistry and aerosols
article

High-Time-Resolution Aerosol Chemistry and Machine-Learning Sensitivity Reveal a Highland Triad Mechanism Driving PM2.5 in Xining (Qinghai–Tibet Plateau)

Weijun Song, Zihong Liang, Xiaofeng Hu, Guojuan Qu, Chunyan Sun, Anan Qi
article en

Abstract

Fine particulate matter (PM2.5) formation mechanisms in fragile highland ecosystems remain inadequately constrained, particularly regarding thermodynamic non-linearities (aerosol pH, liquid water content) and their interaction with geochemical modulation. Here, we present comprehensive year-long online measurements from Xining, Qinghai-Tibet Plateau, integrating hourly measurements of water-soluble ions, inorganic elements, and gaseous precursors with ISORROPIA-II thermodynamic modeling and ensemble machine learning. Median pH was 4.38 but exhibited two distinct pH regimes (14.8% pH < 3.0, 11.5% pH > 7.2), with acute acidification enhancing toxic metal solubility (Fe, Pb by 3-5×), and it posed distinct ecological risks. Our analysis reveals a distinct “highland mechanism triad” governing PM2.5 dynamics: (1) winter meteorological confinement amplifying dust-catalyzed sulfate formation (SOR = 0.68); (2) spring alkaline dust buffering (pH > 7.2) that titrates NH3 and suppresses nitrate formation (NOR < 0.10); and (3) summer photochemical oxidation constrained by chronic NH3 limitation within an oxidant-excess regime. Random Forest achieved optimal prediction for the chemically active inorganic fraction (RMSE = 6.63 μg/m3, R2 = 0.91) by learning regime-specific non-linearities, with local sensitivity analysis identifying Ca2+, SO42−, and Al as chemically sensitive drivers (S > 0.35) while revealing NH3’s seasonally variable influence (rank 15 in winter, significant in summer; S > 0.28), subsequently complemented by global SHAP analysis, which further revealed NO3− as the most robust predictor (ranking 1st–2nd) and captured NH3’s non-linear threshold effects (). Positive Matrix Factorization apportioned secondary aerosols (30.11%) within a unique alkaline–dust matrix. These findings demonstrate that highland PM2.5 inorganic chemistry operates through fundamentally different pathways than lowland photochemical haze, with acid-induced toxic metal activation providing a new target for ecological protection in this fragile ecosystem. Seasonally adaptive mitigation is required: concurrent SO2-NH3 control in winter, dust suppression infrastructure in spring, and agricultural NH3 capture in summer. This integrated framework provides a transferable methodology for air-quality management in alkaline dust-dominated, NH3-limited highland ecosystems (>2000 m).

AtmosphereVol. 17(2)
Qinghai University (CN)
Openalex Percentile: Top 67%
Atmospheric chemistry and aerosols
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