Secondary organic aerosol (SOA), formed via complex chemical mechanisms, is a major contributor to atmospheric aerosol pollution and climate forcing worldwide. Aqueous-phase oxidation serves as an important pathway for SOA formation, with aqueous SOA (aqSOA) exhibiting light absorption across the ultraviolet–visible range. This study investigates the formation and absorption properties of aqSOA in the Sichuan Basin, China. Results indicate that aqSOA mainly originated from aged biomass-burning emissions through aqueous-phase processing rather than from gas-phase photochemical oxidation, particularly under high aerosol liquid water content conditions during pollution periods. Substantial enhancement of brown carbon absorption by SOA was observed between 370 and 660 nm (27.5 %–43.2 %). These findings highlight the significant contribution of aqSOA formation from aged biomass-burning emissions to the brown carbon budget and absorption, especially at night. The mean aerosol absorption Ångström exponents between 370 and 880 nm (AAE370–880) were 1.95, which is higher than the values reported for fresh and photochemically aged biomass-burning emissions. This study elucidates the formation and light-absorbing characteristics of aqSOA derived from aged biomass-burning emissions and highlights the important role of aqueous-phase reactions in aerosol pollution and radiative absorption.
Natural Science Foundation of Chongqing MunicipalityCSTB2022NSCQ-MSX0504National Natural Science Foundation of China42305126National Key Research and Development Program of China2023YFC3709301Introduction
Organic aerosol (OA) constitutes a dominant fraction (20 %–90 %) of atmospheric aerosol, with significant implications for air quality and climate forcing (Jimenez et al., 2009). Field observations consistently indicate that secondary OA (SOA), formed by the atmospheric oxidation of volatile organic compounds (VOCs) and primary OA (POA), accounts for most OA worldwide (Ervens et al., 2011; Huang et al., 2014; Kourtchev et al., 2016). Recent results demonstrate that aqueous-phase oxidation serves as an important pathway for SOA formation, and aqueous SOA (aqSOA) exhibits light absorption across the ultraviolet–visible (UV–Vis) range (Gilardoni et al., 2016; Lim et al., 2010; McNeill 2015; Powelson et al., 2014; Sun et al., 2010). However, the formation mechanisms and absorption properties of aqSOA remain poorly understood, which hinders efforts to improve air quality and reduce uncertainties in global climate estimates.
Several studies suggest that aqSOA represents a major component of SOA formed in fog, clouds and aerosol water (Ervens et al., 2011; Ortiz-Montalvo et al., 2012; Tan et al., 2012; Xu et al., 2022). Oxygenated VOCs with high water solubility and low Henry's law constants, such as methylglyoxal and glycolaldehyde, are important aqSOA precursors (Ortiz-Montalvo et al., 2012; Tan et al., 2012). Limited laboratory studies have demonstrated that levoglucosan and phenolic species produced from biomass burning can also act as aqSOA precursors (Yu et al., 2016; Zhao et al., 2014). Gilardoni et al. (2016) reported direct ambient observations of aqSOA formation from biomass-burning emissions in fog, water and wet aerosol. Additionally, recent studies have reported that aqSOA with high molecular weight (e.g., 4-ethylphenol), formed through aqueous-phase photochemical oxidation, can exhibit strong light absorptivity in the UV range (Herrmann et al., 2015; Ye et al., 2019). Furthermore, previous laboratory studies have demonstrated that certain aqSOA components, such as π-conjugated compounds and imidazoles with C = N bonds, produced by aldol condensation and aqueous-phase carbonyl compound reactions, respectively, strongly absorb light in the near-UV region (Drozd and McNeill, 2014; Kampf et al., 2012; Nozière and Esteve, 2007; Powelson et al., 2014). Despite numerous studies on the formation and optical properties of aqSOA, limited ambient observations still hinder a better understanding of its role in atmospheric chemistry and climate.
China has experienced severe PM2.5 pollution under stagnant high-humidity conditions, during which SOA, a major PM2.5 component, originated largely from fossil fuel combustion and biomass burning (Huang et al., 2014; Wang et al., 2016, 2021; Xu et al., 2022). Field observations indicate that highly oxidized SOA can form through aqueous-phase processing driven by acid-catalyzed oxidation (Meng et al., 2020; Xu et al., 2017), and aqSOA is derived from biomass-burning OA (BBOA) and fossil-fuel OA through aqueous-phase reactions (Wang et al., 2021; Zhao et al., 2019). Limited laboratory studies have reported that aqueous-phase reactions serve as an important oxidation pathway for nitrophenol products such as 5-nitrovanillin and 4-nitroguaiacol, which exhibit strong UV absorption and higher formation and transformation rates in more acidic solutions (Kroflic et al., 2015; Li et al., 2023; Pang et al., 2019; Yang et al., 2021). However, observations of aqSOA formation and optical properties in China remain limited, with most research focusing on the North China Plain (NCP). Similar to the NCP, the Sichuan Basin (SCB), characterized by high humidity and frequent biomass burning, is also the main region with severe aerosol pollution in China (Tian et al., 2019; Wang et al., 2018; Yang et al., 2011).
Previous research has reported that aqSOA from different regions can exhibit distinct formation mechanisms and optical properties due to varying emission sources and ambient conditions (Bao et al., 2023, 2024; Wang et al., 2021; Xu et al., 2017). Wang et al. (2021) reported the rapid aqueous-phase conversion of fossil-fuel primary OA (FF-POA) to aqSOA under high-humidity conditions during a winter haze event in Beijing, China, with the resulting aqSOA exhibiting substantially lower light absorption than its primary precursor due to decreased aromaticity. Similarly, Huang et al. (2023) demonstrated that the aqueous-phase oxidation of fossil fuel combustion emissions played a critical role in SOA formation under high relative humidity (RH) conditions during winter. Xu et al. (2022) reported that biomass burning is a significant non-fossil source of aqSOA under high RH and high aerosol liquid water content (ALWC), especially during the fall-to-winter period, when open burning of post-harvest agricultural crop residues is widespread in China. While aqSOA formation has been extensively studied during winter, autumn – despite featuring both high ALWC and strong biomass-burning emissions – has received considerably less attention (Feng et al., 2022; Qiu et al., 2016; Zhao et al., 2019). In contrast to these studies in the NCP, research in the SCB has reported that the effect of aqueous-phase reactions on oxygenated OA (OOA) formation was significant when ALWC was below 200 µg m−3, but became insignificant when ALWC exceeded 200 µg m−3. Additionally, aqueous-phase oxidation probably did not contribute to the decay of brown carbon (BrC) during summer in the SCB (Bao et al., 2024). In the SCB, autumn is the typical biomass-burning season following the harvest of rape and rice, during which biomass burning contributes significantly more to OA than in other seasons (Chen et al., 2017; Tao et al., 2014; Yang et al., 2019). In summary, the intensive biomass-burning emissions and high ALWC during autumn in the SCB likely result in aqSOA formation pathways that differ from those in other seasons. To date, limited studies have explored the dynamic evolution and optical properties of aqSOA in the SCB, especially during autumn, leaving ambient aqSOA processing poorly understood. Therefore, a more detailed characterization of the aqSOA formation and optical properties is important to reveal the key factors contributing to haze formation in this region.
In this study, a time-of-flight aerosol chemical speciation monitor (ToF-ACSM) and a series of collocated instruments were deployed to characterize the dynamic evolution of aqSOA from biomass burning under real ambient conditions. The study was conducted in a typical city with relatively severe air pollution in the SCB from 21 October to 23 November 2022. Observations revealed that haze formation was significantly driven by BBOA and aqSOA. This study demonstrates that aqSOA forms from aged BBOA through aqueous-phase reactions. Furthermore, the results demonstrate that aqSOA derived from aged BBOA exhibits strong UV absorption and contributes to positive radiative forcing. These results elucidate the formation and light-absorbing properties of aqSOA from aged biomass-burning emissions, providing insights for improved simulations of its atmospheric and climatic impacts.
MethodsSampling site
An intensive field campaign investigating the chemical and physical properties of aerosols was conducted at a site in Yongchuan, China, (29°21′25′′ N, 105°54′6′′ E), a city experiencing severe aerosol pollution, from 21 October to 23 November 2022. This site is representative of an urban environment, surrounded by restaurants, shopping malls, and residential buildings, and is located in a parallel ridge-and-valley area between the two megacities of the SCB (Chongqing center and Chengdu) (Fig. S1 in the Supplement). It is primarily influenced by multiple local emission sources, including traffic (arterial roads 600 m to the east and 300 m to the west) and a variety of residential activities such as biomass burning and fossil fuel combustion. The absence of dynamic interference from neighbouring buildings allowed the measurements to clearly capture the characteristics and evolution of haze pollution at this site.
Instrumentation
During the campaign, non-refractory aerosol (NR-PM2.5) species, including OA, ammonium (NH4), nitrates (NO3), sulfates (SO4), and chlorides (Chl), were measured online using the ToF-ACSM (Aerodyne Research Inc.). Ambient aerosols were pumped into the ToF-ACSM at a flow rate of 3 L min−1 through a PM2.5 cyclone (URG-2000-30ED) and a Nafion dryer (MD-110-48S, Perma Pure, Inc.), reducing the RH to below 30 %. The measurement principle has been described in detail in previous studies (Fröhlich et al., 2013; Ng et al., 2011c).
Aerosol light absorption (Absλ) and equivalent black carbon (BCλ) mass concentrations were measured in real time at seven wavelengths (370, 470, 520, 590, 660, 880, and 950 nm) using an aethalometer (AE33, Magee Scientific). Sampled particles were dried using a Nafion dryer (MD-70024S-3, Perma Pure, Inc.) before measurements. The light attenuation coefficients were converted to Absλ using the real-time compensation parameter, and the nonlinear loading effects of quartz filters were corrected online through parallel measurements of attenuation values (ATN1 and ATN2) (Collaud Coen et al., 2010; Drinovec et al., 2015). The scattering effects of quartz filters were modified automatically by a fixed multiple-scattering parameter (2.14) (Sect. S3 in the Supplement). Detailed measurement methods and principles of AE33 are described in Drinovec et al. (2015).
During the campaign, gaseous species (including O3, NO2, and CO) were continuously measured by gas analyzers (49i, 42i, and 48i, Thermo Scientific) that were maintained and calibrated weekly. Hourly meteorological parameter data, including temperature (T), RH, and PM2.5 mass concentrations, were obtained from the National Environmental Monitoring Station, located near our sampling site (http://www.cnemc.cn/, last access: 30 November 2022).
Data analysisToF-ACSM data analysis
The raw mass spectra data measured by the ToF-ACSM were analyzed using Tofware v2.5.13 (Tofwerk AG) in Igor Pro 6.37 (WaveMetrics, Inc.). The ionization efficiency and relative ionization efficiency (RIE) were regularly calibrated using a scanning mobility particle sizer, consisting of a differential mobility analyzer (SMPS 3081A, TSI) and a condensation particle counter (CPC 3775, TSI). A comprehensive overview of the operation and calibration procedures of the ToF-ACSM is provided in Bao et al. (2023). In accordance with previous studies, the default RIE values for OA, NO3, and Chl were set to 1.4, 1.1, and 1.3, respectively (Canagaratna et al., 2007; Elser et al., 2016). The ionization efficiency value (236 ions per pg) and RIE values of SO4 (1.2) and NH4 (4.3) were estimated from the calibrations of pure ammonium sulfate and ammonium nitrate (ANMF), respectively. Meanwhile, a particle collection efficiency (CE) was introduced to compensate for the particle losses associated with the particle bounce at the vaporizer, which is affected by aerosol acidity, the contribution of ammonium nitrate, and phase state (Matthew et al., 2008). Middlebrook et al. (2012) developed a CE algorithm for the ToF-ACSM to quantify aerosol species. Their results indicated that a constant CE value of 0.45 should be used when: (1) ANMF is below 40 % or (2) particles are either partially or fully neutralized. In this study, aerosol particles were dried using a Nafion dryer (RH <30%) before sampling by the ToF-ACSM, and ANMF was consistently maintained below 40 %. As shown in Fig. S2, the average ratio of the measured NH4 to the predicted NH4, which is required to fully neutralize SO4, NO3, and Chl, was approximately 1. Under these conditions, the CE value typically used at this site was not affected. The typical default CE value (0.5) was applied throughout the sampling period, which was consistent with previous research (Bao et al., 2025; Peng et al., 2025; Sun et al., 2016a, b; Zhao et al., 2019). While the typical default CE is 10 % higher than 0.45, the difference is small, considering the 30 % uncertainty determined for CE (Bahreini et al., 2009). Additionally, the strong correlation between NR-PM2.5 and PM2.5 mass concentrations supports the validity of the CE value (Fig. S3).
The mass spectral matrix of OA for m/z 10–120 was analysed through positive matrix factorization (PMF) with the multilinear engine (ME-2) implemented in SoFi (Source Finder, version 6.3) (Canonaco et al., 2013; Paatero, 1999; Paatero and Tapper, 1994). Briefly, an unconstrained PMF analysis was performed to determine the number and types of source factors. Subsequently, the constrained ME-2 approach was applied to minimize rotational ambiguity by testing a-values from 0 to 1 in steps of 0.1 (Elser et al., 2016; Wang et al., 2019b; Zhong et al., 2021). Ions with a signal-to-noise ratio (SNR) below 0.2 were discarded, whereas those with an SNR between 0.2 and 2 were downweighted by a factor of 2 (Bao et al., 2023; Paatero and Hopke, 2003). Finally, five OA factors were resolved with the rotational parameter set to zero (fpeak=0), including three POA factors (BBOA, coal-combustion OA (CCOA), and hydrocarbon-like OA (HOA)) and two SOA factors (OOA and aqSOA) (Figs. S9 and S10). Detailed diagnostic plots of the PMF results are presented in the Supporting Information (Figs. S4–S10), and the details of OA source apportionment procedures are described in Sect. S1.
Aerosol liquid water content
ALWC is controlled by meteorological conditions (T and RH) as well as by inorganic and OA components. During the campaign, ALWC controlled by the inorganic fraction was estimated with the ISORROPIA-II thermodynamic model, based on mass concentrations of ammonium, nitrate, sulfate, and chloride measured by the ToF-ACSM, together with the meteorological parameters (T and RH) from the National Environmental Monitoring Station (Fountoukis and Nenes, 2007). The calculations were performed in forward type and metastable mode within ISORROPIA-II (Hennigan et al., 2015). The model simulated the thermodynamic equilibrium of the NH4+-SO42--NO3--Cl−-H2O system and subsequently calculated the ALWC. Following established methods, the organic contribution to ALWC was estimated using the Zdanovskii-Stokes-Robinson mixing rule, as discussed in Sect. S2 (Guo et al., 2015; Huang et al., 2020; Nguyen et al., 2016; Xu et al., 2022). In this study, the ALWC with organic species ranged from 0.1 to 35.2 µg m−3, with an average of 1.9±3.0µg m−3, accounting for 3.7±2.2% of total ALWC. As organic species had minor effects on total ALWC (<5%), the ALWC was determined only considering inorganic species (Chen et al., 2021; Guo et al., 2015; Liu et al., 2017).
Light absorption measurements
The Absλ was partitioned into contributions from BC and BrC, a group of colored OA compounds, denoted as Absλ,BC and Absλ,BrC, respectively, such that Absλ=Absλ,BC+Absλ,BrC, and characterized by the absorption Ångström exponent (AAE) (Laskin et al., 2015). Here, Absλ was derived from BCλ mass concentrations at each wavelength using the mass absorption cross-section (MACλ) (Absλ=BCλ×MACλ), with MACλ values assumed to be 18.47, 14.54, 13.14, 11.58, 10.35, 7.77, and 7.19 m2 g−1 at 370, 470, 520, 590, 660, 880, and 950 nm, respectively (Drinovec et al., 2015; Zhu et al., 2017). Absorbance at 880 nm (Abs880) was attributed solely to BC. The following formula was used to determine Absλ,BC values (Drinovec et al., 2015; Kirchstetter and Novakov, 2004; Moosmüller et al., 2009; Qin et al., 2018; Wang et al., 2021; Zhu et al., 2017):
1Absλ,BC=Abs880×880/λ-AAEBC2AAEBC=log10(Abs880/Abs950)÷log10(880/950)
A detailed description of Absλ,BC and Absλ,BrC calculations is provided in Sect. S3. Previous studies have demonstrated that AAEBC is sensitive to the refractive index, size distribution, and coating state of carbonaceous aerosols (Gyawali et al., 2009; Lack and Langridge, 2013; Li et al., 2019). In this study, the uncertainties in AbsBC and AbsBrC estimations were analyzed (Sect. S3). The relative uncertainties of AbsBC and AbsBrC were [-46%, +21%] and [-112%, +42%] at 370 nm, respectively. Absλ,BrC comprises contributions from primary and secondary BrC (Absλ,BrC,pri and Absλ,BrC,sec). Absλ,BrC,sec was calculated using the minimum R-squared method (MRS) at each wavelength (Wang et al., 2019b; Wu and Yu, 2016; Wu et al., 2024). Further details on the MRS method and Absλ,BrC,sec estimation are provided in Sect. S3.
The light absorption contribution of each OA component at each wavelength, as analyzed using multiple linear regression (Qin et al., 2018; Xie et al., 2019), is expressed as follows:
AbsBrC=a×OOA+b×BBOA+c×CCOA+d×aqSOA+e×HOA.
where [OOA], [BBOA], [CCOA], [aqSOA], and [HOA] denote the mass concentrations of the corresponding OA components. Coefficients a–e are constants used to optimize the Absλ of each OA component and are equivalent to MAC values at each wavelength (i.e., a–e at 370 nm represented MAC370,OOA, MAC370,BBOA, MAC370,CCOA, MAC370,aqSOA, and MAC370,HOA, respectively). Here, the normalized mean bias, root mean square error, and index of agreement were used to evaluate the performance of the multiple linear regression method (Sect. S4) (Li et al., 2011). The index of agreement values for Abs370,BrC and Abs470,BrC were 0.99 and 1.00, respectively, both exceeding 0.95. The slopes of the linear regression between the AE33-measured and MLR-estimated absorption coefficients were 0.81 and 0.96 for Abs370,BrC and Abs470,BrC (close to unity), respectively. These results indicate good agreement between the AE33 measurement and the MLR-reconstructed Abs370,BrC.
Time series of (a) RH and T, (b) NR-PM2.5 species measured by the ToF-ACSM and BC, (c) Abs370,BrC and MAC370,BrC, and (d) mass fractions of OA factors during the campaign. The pollution period (BC + NR-PM2.5>75µg m−3) is highlighted by the shaded areas.
Results and discussionEnhanced OA formation from BBOA and aqSOA during pollution periods
The temporal variations of PM2.5 species concentrations, meteorological parameters, Abs370,BrC and MAC370,BrC during the campaign are shown in Fig. 1. Wind speeds were consistently low (0.3±0.2 m s−1), indicating stagnant atmospheric conditions throughout the study period. The average concentrations of O3 and NO2 during the campaign were 24.8 ± 16.1 and 14.2 ± 6.8 ppb, respectively. The total PM2.5 (BC + NR-PM2.5) mass concentrations ranged from 7.0 to 175.5 µg m−3, with an average of 48.4 ± 27.8 µg m−3. The average concentrations of OA, NO3, SO4, NH4, Chl, and BC were 24.1 ± 18.1, 8.3 ± 6.2, 6.2 ± 3.4, 5.2 ± 2.7, 0.2 ± 0.1, and 4.7 ± 2.9 µg m−3, accounting for 46.6 ± 10.7 %, 17.7 ± 8.0 %, 13.2±4.4 %, 11.2 ± 2.7 %, 0.3 ± 0.2 %, and 10.1±5.5% of total PM2.5, respectively. OA accounted for the largest fraction of PM2.5, highlighting its significant contribution to PM2.5 pollution in the SCB (Bao et al., 2023; Wang et al., 2018). The OA fractions of PM2.5 in this study are comparable to those reported in wintertime studies in the SCB and are significantly higher than those observed in winter in other Chinese regions (Table S1 in the Supplement). Meanwhile, elevated levels of Abs370,BrC and MAC370,BrC, ranging from 5.8 to 210.2 Mm−1 (42.4 ± 28.5 Mm−1) and from 0.6 to 7.0 m2 g−1 (2.1 ± 0.9 m2 g−1), respectively, were observed during the campaign.
According to the Chinese National Ambient Air Quality Standard (GB 3095-2012) (MEE, 2012), the Grade I and Grade II 24 h limits for PM2.5 are 35 and 75 µg m−3, respectively. The Grade II limit, based on the WHO Phase-1 interim target (IT-1), is higher than the WHO Air Quality Guideline value (15 µg m−3), the EU daily limit (25 µg m−3), and the U.S. 24 h standard (35 µg m−3). During the campaign, the mean PM2.5 concentration was 1.4 times the Grade I limit (35 µg m−3). Pollution periods (PP) were defined as days with daily PM2.5 mass concentrations exceeding the Grade II limit (75 µg m−3), whereas days with PM2.5 below 75 µg m−3 were defined as clean periods (CP). During PP, the average mass concentrations of BC + NR-PM2.5 and OA were 2.5 and 3.1 times those during CP, respectively, corresponding to 102.3 ± 26.9 and 57.4 ± 22.5 µg m−3. As shown in Fig. 2, the chemical composition of PM2.5 differed substantially between PP and CP. Compared with other species, a significantly higher contribution of OA was observed during PP (56.6 %) than during CP (46.6 %) (Student's t-test, p<0.001) (Fig. 2).
In this study, five OA factors were resolved using the PMF model. More details are provided in Sect. S1, and the mass spectra of these factors are shown in Fig. S9. HOA was characterized by alkyl fragment ion series at CnH2n-1+ and CnH2n+1+ (m/z 41, 43, 55, and 57), which are typical of primary combustion emissions (Elser et al., 2016; Lanz et al., 2007). BBOA was identified by prominent signals at m/z 60 (mainly C2H4O2+) and m/z 73 (mainly C3H5O2+), which correspond to fragments of levoglucosan and mannosan from incomplete biomass burning (Alfarra et al., 2007). CCOA showed high signals of unsaturated hydrocarbon ion fragments such as PAH-related ion fragments (m/z 77, 91, 115), indicative of traditional coal combustion (Sun et al., 2016a). OOA was distinguished by a dominant signal at m/z 44 (mainly CO2+) and a strong correlation with oxygenated ions (Ng et al., 2011b). AqSOA also correlated strongly with oxygenated ions, such as m/z 43 (mainly C2H3O+) and m/z 44, and exhibited a notably higher signal at m/z 29 (mainly CHO+) than other OA factors, consistent with previous reports (Sun et al., 2016a; Xu et al., 2019; Zhao et al., 2019; Zhong et al., 2021). Moreover, BBOA correlated strongly with m/z 60 (mainly C2H4O2+) and m/z 73 (Pearson's r2 (r2) =0.85, 0.80, p<0.001); CCOA was strongly correlated with Chl and m/z 115 (r2=0.56, 0.48, p<0.001); HOA correlated with NO2 and m/z 41 (r2=0.47, 0.59, p <0.001); and OOA and aqSOA were significantly correlated with NO3/NH4 (r2=0.77, 0.75, p<0.001) and SO4/ALWC (r2=0.67, 0.85, p<0.001), respectively (Fig. S10). These results confirm the robustness and physicochemical plausibility of the five OA factors identified in this study. Overall, the average concentration of BBOA was 8.6 ± 7.7 µg m−3 and accounted for the highest proportion of OA (34.8 ± 11.2 %), followed by OOA (5.5 ± 3.5 µg m−3, 21.7 ± 11.4 %), CCOA (4.0±3.3µg m−3, 15.7 ± 7.1 %), HOA (3.5 ± 2.8 µg m−3, 14.6 ± 8.1 %), and aqSOA (3.3 ± 2.9 µg m−3, 13.2 ± 5.9 %) (Fig. 1). These results identified BBOA as the dominant component of OA in autumn in the SCB. Notably, the fraction of BBOA in OA in this study was much higher than those reported in wintertime studies in China (Table S1).
The contributions of BBOA and aqSOA to OA increased from CP (31.7 % and 12.6 %, respectively) to PP (38.6 % and 14.1 %, respectively), whereas those of CCOA, HOA, and OOA decreased. Significantly higher RH and ALWC were observed during PP (58.5 ± 12.4 % and 69.4 ± 30.3 µg m−3, respectively) than during CP (49.8 ± 8.9 % and 37.1±20.8µg m−3, respectively) (p<0.001), whereas temperature showed no significant difference (p>0.1). The average wind speed during CP was 1.3 times that during PP, reaching 0.32±0.18 m s−1. These results indicate that the atmosphere during PP was characterized by stagnation, higher RH, and elevated ALWC, likely leading to distinct sources and chemical processing of OA compared with CP.
Diurnal variations of PM2.5 species, BC, OA factors, m/z 29, m/z 60, and m/z 115 mass concentrations during the (a) clean period (CP) (BC + NR-PM2.5<75µg m−3) and (b) pollution period (PP) (BC + NR-PM2.5>75µg m−3). The pie charts on the left side of panels (a) and (b) show the average mass contributions of different chemical compositions to BC + NR-PM2.5 during CP and PP, respectively. Meanwhile, the average mass contributions of OOA, BBOA, CCOA, aqSOA, and HOA to OA are shown in the pie charts in the middle of panels (a) and (b), respectively.
Compared with CP, OA concentration exhibited an evident diurnal variation during PP. As shown in Fig. 2, the OA concentration peaked at 12:00 local time (LT) (82.7 µg m−3) during daytime in PP, whereas in CP, the peak occurred at 21:00 LT. During PP, OA increased rapidly at a rate of 7.8 µg m−3 h−1 from 09:00 to 12:00 LT, accompanied by a significant decrease in NO3. BBOA and aqSOA concentrations exhibited similar diurnal patterns to OA, with high values during daytime and a rapid increase from 09:00 to 12:00 LT during PP. Previous studies have indicated that the aqSOA mass spectrum showed a higher signal at m/z 29 (CHO+) than other OA factors (Gilardoni et al., 2016; Meng et al., 2020; Wang et al., 2021). During PP, the tracer ion fragments for BBOA (m/z 60) and aqSOA (m/z 29) peaked at 12:00 LT (1.2 µg m−3) and 13:00 LT (4.3 µg m−3), respectively. Additionally, ALWC correlated more strongly with aqSOA concentration (r2=0.86, p<0.001) than with BBOA concentration (r2=0.58, p<0.001). Both ALWC and aqSOA concentrations peaked at 13:00 LT, later than the BBOA peak (12:00 LT), supporting that ALWC might play a significant role in the chemical processing that converts BBOA to aqSOA during PP. In contrast, odd oxygen (Ox= O3+ NO2) showed weak correlations with both OOA and aqSOA concentrations throughout the campaign (p>0.1, data not shown). Although the average Ox concentration was higher during PP (51.1 ± 19.6 ppb) than during CP (36.9 ± 14.0 ppb), no significant correlation was observed in either period. These results suggest that gas-phase photochemical oxidation might played a limited role in SOA formation in this study.
In summary, these results suggest that OA was the dominant component of PM2.5, especially during PP in the SCB. During PP, BBOA and aqSOA contributed significantly to the daytime increase in OA concentration. Previous studies have shown that the autumn harvest period – specifically October and November – is characterized by intensified biomass burning in the SCB, primarily due to post-harvest crop-residue burning (Chen et al., 2017; Tao et al., 2014). Thus, daytime aqSOA formation during PP might be related to high aerosol water content and BBOA emissions (Bao et al., 2023; Chen et al., 2017, 2019; Tao et al., 2014). Additionally, Gilardoni et al. (2016) found that aqSOA, such as guaiacol dimer (C14H14O4+), could be formed from aged biomass-burning emissions in both fog water and wet aerosol, especially under high ALWC conditions. To further explore the formation of aqSOA from biomass-burning emissions through aqueous-phase reactions, the next section discusses the dynamic evolution of aqSOA in relation to BBOA.
Biomass-burning emissions as precursors for aqSOA
Figure 3 shows a strong positive correlation between the mass fraction (%) of aqSOA in total PM2.5 and ALWC during the campaign (r2=0.64, p<0.001). The contribution of aqSOA increased with increasing f29 values (the normalized signal at m/z 29). Notably, the aqSOA factor showed significantly higher f29 and f60 values (0.167 and 0.011, respectively) than the OOA factor (0.017 and 0.002, respectively) (Fig. S9). Moreover, both aqSOA concentrations and f29 were strongly correlated with ALWC (r2=0.85, 0.73, p<0.001) (Fig. 3). The average oxygen-to-carbon ratio (O : C) of the aqSOA factor (0.85) was 2.7 times that of the BBOA factor (0.31), whereas the hydrogen-to-carbon (H : C) ratios were similar (1.74 for aqSOA and 1.81 for BBOA), indicating the replacement of a hydrogen atom by an OH moiety (Lim et al., 2010; Ng et al., 2011a). These results were similar to aqSOA results in Italy and Beijing (Gilardoni et al., 2016; Zhao et al., 2019).
Scatter plot of the mass fraction of aqSOA in BC + NR-PM2.5 versus ALWC, coloured by f29 (normalized signal at m/z 29) during the campaign. f29 (mainly CHO+) is a tracer for alcohol compounds and is used to monitor the aqueous-phase oxidation of organic compounds, such as glyoxal.
Previous studies indicate that aqueous-phase processes contribute to SOA formation from fossil fuel emissions (Ervens et al., 2011; Huang et al., 2023; Wang et al., 2021; Xu et al., 2022; Yan et al., 2017). Wang et al. (2021) and Xu et al. (2022) have highlighted the role of aqueous-phase reactions in SOA formation, particularly in regions with substantial anthropogenic emissions. In this study, a strong anticorrelation was observed between the mass fraction of fossil-fuel-related OA components (sum of CCOA, HOA and OOA) and ALWC at high f29 values (r2=0.48, p<0.001, data not shown), consistent with recent findings (Wang et al., 2021). This indicates that aqSOA may also be produced by aqueous-phase reactions of fossil-fuel-related OA components.
Variations of (a) OA factor mass concentrations, (b) OA mass concentrations, f29 (a tracer for alcohol compounds), and mass fraction of OA factors as a function of ALWC. Data were grouped into different bins according to a 10 µg m−3 increment of ALWC.
Figure 4 shows the relationships between ALWC and the concentrations of OA factors as well as f29 during the campaign. The mass concentrations of all five resolved OA factors increased with increasing ALWC. However, compared with other OA factors, aqSOA and BBOA increased more significantly, from 1.1 and 4.9 to 5.2 and 10.8 µg m−3, respectively, when 20 µg m−3< ALWC <60µg m−3. Notably, only the aqSOA concentration continued to rise under high ALWC conditions (>100µg m−3). This enhancement likely resulted from the formation of more water-soluble organic species, such as glyoxal and methylglyoxal, which were subsequently oxidized to aqSOA via aqueous-phase reactions in aerosol liquid water (Carlton et al., 2007; Ervens et al., 2011; Tan et al., 2012).
As shown in Fig. 4b, the mass fraction of aqSOA increased significantly from 5 % at ALWC <20µg m−3 to 17 %–22 % at ALWC >60µg m−3, accompanied by a corresponding decrease in the OOA fraction. In contrast, the contributions of POA (BBOA + CCOA + HOA) and SOA (OOA + aqSOA) remained relatively stable across different ALWC levels (58 %–68 % and 32 %–42 % for POA and SOA, respectively). This result suggests aqSOA forms more intensively than OOA through aqueous-phase reactions, although it may also be formed from OOA, consistent with recent studies in northwestern China (Zhao et al., 2019; Zhong et al., 2021).
Furthermore, f29 (CHO+) increased from 0.010 to 0.227 as a function of ALWC (Fig. 4b). A pronounced rise in f29 from 0.055 to 0.210 occurred when ALWC increased from 60 to 100 µg m−3 (p<0.001), tracking the concurrent increase in OA mass concentrations (13.2–109.1 µg m−3). Previous laboratory analyses of organic standards have found that species without alcohol groups showed low f29 (<0.05), while polyols and species with non-acid OH groups, which are common products of biomass-burning emissions, displayed high f29 values (0.05–0.15) (Canagaratna et al., 2015; Gilardoni et al., 2016; Zhao et al., 2014). This further supports the potential formation of organic compounds with hydroxyl groups, such as glyoxal and methylglyoxal, under high ALWC conditions. Overall, these results demonstrate that the observed aqSOA could be formed predominantly from biomass-burning emissions through aqueous-phase reactions, reinforcing the important role of BBOA in increasing PM2.5 mass concentration.
Scatter plots of aqSOA versus (a, b) BBOA and (c, d) OOA mass concentrations, coloured by ALWC during CP and PP. The size of the symbols panel in (b) and (d) increases with the increase in the f29 value, which is a tracer for alcohol compounds.
To identify the formation of aqSOA and its precursors under different PM2.5 pollution levels, the relationships between aqSOA and BBOA or OOA mass concentrations, as well as key ion-fragment tracers, were analyzed separately during CP and PP. The correlation (r2) between aqSOA and BBOA was stronger during PP (0.64) than during CP (0.54) (p<0.001, Fig. 5a, c). Although both aqSOA and BBOA concentrations increased with increasing ALWC during both periods, the correlations of ALWC with aqSOA and BBOA were relatively stronger during PP than during CP (p<0.001). As shown in Fig. 5b, d, f29 was highly correlated with aqSOA formation during both CP and PP. A subset of data points with high aqSOA and OOA concentrations displayed relatively low f29 values (0.071–0.102), as shown in Fig. 5d. For these points, the average value of f44 (normalized signal of m/z 44) (0.103 ± 0.024) was 1.3 times that of the overall dataset (0.080 ± 0.035) during PP, likely due to the formation of more-oxidized OOA under high ALWC values (>80µg m−3) (Xu et al., 2017). Previous studies have found that f29 values for polyols and species with non-acid OH groups from biomass-burning emissions were typically lower than 0.15 (Canagaratna et al., 2015; Gilardoni et al., 2016; Zhao et al., 2014). Moreover, the mass fraction of aqSOA showed a stable increasing trend and remained elevated (from 18 % to 22 %) at ALWC >80µg m−3, accompanied by a corresponding decrease in OOA (from 15 % to 10 %) (Fig. 4b). In contrast to OOA (p>0.1), aqSOA concentration showed a strong positive correlation with ALWC (r2=0.73, p<0.001) when ALWC >80µg m−3 during PP. However, no such correlations were observed during CP (p>0.1). Notably, a strong anticorrelation between aqSOA and OOA concentrations was observed during PP at ALWC >80µg m−3 when f29>0.15 (r2=0.76, p<0.001), but not during CP (p<0.1) (Fig. 5b, d). These results indicated that aqSOA formation was more intensive than OOA at high ALWC levels during PP.
Previous research demonstrated that f44 could be used as a tracer for aged SOA, f43 (normalized signal at m/z 43) for POA and fresh SOA, and f60 (presence of anhydrosugars) for BBOA (Cubison et al., 2011; Ng et al., 2010). Additionally, m/z 44 and 43 are typically from different functional groups, and their ratio changes as a function of atmospheric aging. The triangle plot of f44 versus f43 has been widely used to characterize OA evolution, whereas that of f44 versus f60 is commonly used to track the aging of BBOA (Ortega et al., 2013; Paglione et al., 2020; Xu et al., 2017, 2019). In this study, the bottom region of the triangle (Fig. 6) was dominated by BBOA, CCOA, and HOA, which exhibited low f44 (0.040, 0.017, and 0.016, respectively), indicating fresh, less-oxidized emissions. In contrast, the f44 of SOA factors (OOA and aqSOA; 0.118 and 0.117, respectively) were observably higher, reflecting their oxidized nature. The f44 of aqSOA was close to that observed in fog (Gilardoni et al., 2016; Kim et al., 2019), highlighting the role of aqueous-phase reactions in this study. Moreover, the relative abundance of m/z 45 (mainly HCO2+), a tracer ion for carboxylic acids, was higher in the aqSOA spectrum than in the OOA spectrum (Fig. S9), consistent with previous findings that aqueous-phase reactions are important sources of oxygenated organic compounds, including organic acids (Ervens et al., 2011; Kim et al., 2019; McNeill, 2015; Sun et al., 2010; Yu et al., 2014). As shown in Fig. 6b, BBOA and aqSOA displayed higher f60 values (0.019 and 0.011, respectively) than CCOA (0.009) and HOA (0.008). The f60 value of OOA was 0.002, which is lower than the typical background level (0.003) observed in the atmosphere unaffected by biomass burning (Cubison et al., 2011). The mass spectrometry feature of aqSOA, characterized by elevated f44 and f60 values, placed it in the schematic region of aged BBOA reported in previous studies (Cubison et al., 2011; Ortega et al., 2013). Additionally, BBOA contains abundant water-soluble organic compounds, such as sugars, phenols, and organic acids, that can efficiently form aqSOA through aqueous-phase reactions, such as oxidation and oligomerization reactions (Ervens et al., 2011; Gilardoni et al., 2016; Lee et al., 2013; Lei et al., 2024; Li et al., 2020; Powelson et al., 2014). In contrast, OOA formation primarily relies on the gas-phase oxidation of VOCs with high-reactivity, such as aromatics and long-chain alkanes, by OH radicals, which have low concentrations in BBOA plumes (Akagi et al., 2011; Jimenez et al., 2009; Shrivastava et al., 2017; Yokelson et al., 2007). This suggests that BBOA acts as an important precursor for aqSOA instead of OOA through aqueous-phase reactions. These results are consistent with previous studies, and most of the observed data fall within the triangle space (Bao et al., 2023; Kim et al., 2019; Paglione et al., 2020). Notably, aqSOA formation processes can be more intense and significant during autumn due to elevated precursor concentrations (e.g., BBOA), ALWC, and RH values, though the underlying chemical pathways are robust and can occur year-round (Bao et al., 2023; Tang et al., 2025; Zeng et al., 2025).
Triangle plots of (a, c)f44 (normalized mass spectrum signal at m/z 44) versus f43 (normalized mass spectrum signal at m/z 43) and (b, d)f44 versus f60 (normalized mass spectrum signal at m/z 60), coloured by ALWC (circles) during CP and PP. The dashed lines in (a) and (c) were derived from Ng et al. (2010) and used to follow the aging of OA components in the atmosphere. The background space (f60<0.003) without biomass burning influence is also shown by the grey shaded area. The background value of secondary aged OA (brown dashed line) and the black dashed lines characterizing the aging of BBOA in (b) and (d) were derived from Cubison et al. (2011). The data points (squares) included the measurements from this study (bordered in red) and previous research (Bao et al., 2023; Gilardoni et al., 2016; Kim et al., 2019; Ng et al., 2011a; Paglione et al., 2020; Xu et al., 2015, 2017, 2019; Zhao et al., 2017, 2019). f43 (mainly C2H3O+) is a tracer for POA and fresh SOA; f44 is a proxy of the OA oxygenation degree and used as a tracer for aged SOA; and f60 is a proxy of anhydrosugars emitted from biomass burning.
During PP, f44 values ranging from 0.022 to 0.140 (0.080 ± 0.035) were significantly higher than those during CP (0.021–0.150, 0.064 ± 0.019) (p<0.001), whereas f43 was slightly lower, with an average of 0.062 ± 0.027. Compared with CP (r2=0.17, slope =-0.53), f44 showed a more pronounced inverse relationship with f43 during PP, characterized by a higher r2 value (0.70) and a regression slope closer to -1 (-1.09). This pattern indicated a greater abundance of aged SOA in the atmosphere during PP (Fig. 6a and c). Notably, data points in the f44–f43 space during PP fell within the upper boundary of the triangle region, with most points located outside the bottom boundary. These results suggested that less oxidized SOA was predominantly formed through aqueous-phase processing instead of gas-phase photochemical oxidation during PP (Kim et al., 2019; Zhao et al., 2019). Moreover, points outside the bottom boundary of the triangle region, characterized by higher f44 (>0.05) and lower f43 (<0.06), were associated with relatively higher ALWC during PP, a feature not observed during CP.
Here, the triangle plots of f44 versus f60, coloured by ALWC under different PM2.5 pollution levels, were analyzed (Fig. 6b, d), while the link between aqSOA and BBOA was further stressed by a schematic representation of aged BBOA. Except for a few outliers, f60 values were consistently higher than 0.003, and most data points fell within the triangular region, suggesting a widespread influence of biomass burning on OA. During PP, f60 ranged from 0.005 to 0.019 (0.010 ± 0.004), similar to the range observed in CP (from 0.004 to 0.019, 0.010 ± 0.003). However, the correlation between f44 and f60 was higher during PP (r2=0.72) than during CP (r2=0.31) (p<0.001). Moreover, data points within the schematic space of aged BBOA showed relatively higher ALWC compared with the overall dataset during PP, a pattern that was not evident during CP.
Regional transport significantly influenced the aging of BBOA in the SCB. Previous studies have demonstrated that northeast winds prevail during autumn in this region, facilitating the transport of pollutants along the Dazhou→Guang'an→Hechuan pathway, and this northeast-southwest transport pathway had a significant impact on Chongqing (Peng et al., 2019; Wang et al., 2018). As shown in Fig. S11, air masses during the campaign predominantly originated from northeastern Chongqing, an area with widespread agricultural burning activities (He et al., 2015; Luo et al., 2020), and were transported over relatively short distances. Compared to other air mass clusters, the highest contribution and concentration of BBOA to total PM2.5 were observed when air masses passed through northeastern Chongqing. The percentage of air mass trajectories that passed through biomass-burning-influenced regions was higher during PP (∼ 57 %) than during CP (∼ 35 %). Unlike Cluster 3 during CP, air masses originating from northeastern Chongqing (Cluster 2) during PP showed significantly higher contributions and concentrations of BBOA (24.7 %, 27.8 µg m−3) and aqSOA (9.4 %, 10.6 µg m-3) than other clusters (p<0.001). In addition, Cluster 2 exhibited notably higher values of ALWC (93.7 µg m−3), Abs370,BrC,sec (105.1 Mm−1), f44 (0.113), and the NO3/ SO4 ratio (2.1, a tracer for BBOA aging (Liu et al., 2024; Zhang et al., 2025)) than other clusters during PP (p<0.001). During PP, approximately 68 % of the trajectories in Cluster 2 passed through biomass-burning-influenced regions, with transport times to the sampling site ranging from 12 to 48 h, consistent with the typical timescale for aqueous-phase aging of biomass-burning emissions reported in earlier works (Cubison et al., 2011; Hennigan et al., 2010; Ortega et al., 2013; Zhu et al., 2023). These results suggest that regionally transported BBOA, primarily originating from northeastern Chongqing, underwent aging to form aqSOA within approximately 12–48 h.
Evolution of BrC Absorption
Previous research indicates that OA from both fresh and aged biomass-burning emissions exhibits light absorption across the UV–Vis range, with significantly higher AAE values than BC, and may contribute to net positive radiative forcing (Laskin et al., 2015). In this study, the absorption properties of BrC and their relationships with the five OA factors were analyzed. The values of Absλ,BrC,pri and Absλ,BrC,sec were obtained using the MRS method, and the Abs value of each OA factor at each wavelength was estimated using the MLR method (Sects. S3 and S4). The mean Abs370,BrC was 42.4 ± 28.5 Mm−1 (accounting for 49.2 % of Abs370), much higher than Abs660,BrC (2.6 ± 1.3 Mm−1, 10.5 %), suggesting high absorption efficiency for BrC in the near-UV region. From 370 to 660 nm, Absλ,BrC,pri and Absλ,BrC,sec accounted for 56.8 %–72.5 % and 27.5 %–43.2 % of Absλ,BrC, respectively, indicating that primary emissions were the dominant contributors to BrC absorption (Fig. S13). However, the contribution of Absλ,BrC,sec to Absλ,BrC increased with wavelength, suggesting that the impact of SOA on AbsBrC should not be ignored. The following analysis demonstrates that aqSOA formed from aged BBOA contributed substantially to the BrC budget and exhibited strong light absorption across the UV–Vis range.
Data at 370 nm, which exhibit higher SNRs and a greater contribution of AbsBrC, were selected to further analyze the correlations of BrC absorption with various OA components. As described in Sect. 2.3.3, the Abs of the five OA factors at each wavelength were obtained using the MLR method (Table S2). The contributions of BBOA (Abs370,BBOA) and aqSOA (Abs370,aqSOA) to Abs370,BrC were 51.9 % and 16.4 %, respectively, exceeding those of CCOA (11.5 %), HOA (9.1 %), and OOA (11.1 %). This pattern is consistent with the higher MAC values of BBOA and aqSOA (Fig. S15).
Figure S16 presents correlations between Abs370,BrC and the mass concentrations of OOA, BBOA, CCOOA, aqSOA, HOA, and the tracer ion m/z 60 (ion fragment tracers of BBOA). Abs370,BrC exhibited the strongest positive correlations with BBOA and m/z 60 (r2=0.77, p<0.001), followed by aqSOA (r2=0.69, p<0.001). In contrast, correlations with HOA (r2=0.36), CCOA (r2=0.25), and OOA (r2=0.09, p>0.1) were much weaker. Among all OA factors (excluding BBOA), aqSOA contributed relatively more to Abs370,BrC (Table S2) and also displayed a stronger correlation with Abs370,BrC. These results may be related to the formation of aqSOA from aged BBOA via aqueous-phase reactions. Gilardoni et al. (2016) demonstrated that aqSOA derived from aged BBOA through aqueous-phase reactions. Gilardoni et al. (2016) demonstrated that aqSOA derived from aged BBOA through aqueous-phase reactions in the ambient atmosphere contributes to the BrC budget and exhibits slightly higher AAE467–660 (AAE of aerosols from 467 to 660 nm) values than fresh or processed biomass-burning emissions in laboratory experiments.
The MAC values of the five resolved OA components (equivalent to coefficients a–e in the MLR method) at different wavelengths are shown in Fig. S15. At 370 nm, BBOA showed the highest MAC (2.37 m2 g−1), followed by aqSOA (1.23 m2 g−1), indicating that oxidation of BBOA to aqSOA reduces light absorption at shorter wavelengths. Previous research found that the MAC of BBOA at 365 nm is twice that of SOA, which was associated with water-soluble BrC (Lorenzo et al., 2017; Washenfelder et al., 2015). The AAE values of the OA factors, calculated by a power-law fitting of their Abs from 370 to 660 nm (Qin et al., 2018; Wang et al., 2019b), are shown in Fig. S15. Notably, aqSOA had the lowest AAE370–660,aqSOA value (3.54), whereas BBOA had the highest AAE370–660,BBOA value (4.93). Moreover, the contribution of aqSOA to AbsBrC increased from 16.4 % at 370 nm to 26.7 % at 660 nm, whereas that of BBOA decreased from 51.9 % to 39.1 % over the same wavelength range. These findings suggest that aqSOA formed from aged BBOA significantly contribute to the light absorption of BrC in the UV–Vis range.
(a) Ternary diagram for the mass fractions of BBOA, CCOA, and HOA in POA, coloured by Abs370,BrC,pri, and (b) scatter plot of BBOA mass concentrations versus Abs370,BrC,pri, coloured by m/z 60 mass concentrations.
Figure 7 shows a ternary contour map that quantifies the contributions of BBOA, CCOA, and HOA to Abs370,BrC,pri. A strong positive correlation (p<0.001) and a steep linear regression slope (1.80) were observed between the BBOA mass concentration and Abs370,BrC,pri. Among these POA factors, high mass fractions of BBOA relative to POA were consistent with high values of Abs370,BrC,pri (Fig. 7a). For example, most data points with Abs370,BrC,pri higher than 49.1 Mm−1 (90th percentile of Abs370,BrC) fell within the region of high BBOA/POA values (>0.5). Moreover, Abs370,BrC,pri increased significantly with increasing BBOA and m/z 60 mass concentrations, exhibiting higher correlation coefficients (r2=0.63 and 0.55) than HOA (r2=0.19) and CCOA (r2=0.14) (Fig. 7b). These results indicate the major contribution of BBOA to primary BrC light absorption at 370 nm.
To understand the relationship between secondary BrC absorption and its chromophores, the correlation between Abs370,BrC,sec and the mass concentrations of SOA factors was analyzed. As shown in Fig. S17, Abs370,BrC,sec increased significantly with increasing aqSOA concentration (r2=0.44, p<0.001), and high Abs370,BrC,sec values were associated with elevated ALWC. In contrast, no such relationship was found for OOA (p>0.1). The slope of the linear regression between aqSOA mass concentrations and Abs370,BrC,sec (3.50) was steeper than that for OOA (Fig. S17), and the MAC values of aqSOA were also higher across the UV–Vis range (Fig. S15).
Scatter plots of Abs370,BrC,pri/ΔCO versus (a, b) BBOA and m/z 60 mass concentrations and Abs370,BrC,sec/ΔCO versus (c, d) aqSOA and ALWC, coloured by the local time.
To further characterize the evolution of secondary BrC absorption, Abs370,BrC,sec was normalized by ΔCO (background-corrected CO mixing ratios) to minimize the effect of boundary layer height (Fig. 8) (DeCarlo et al., 2010). Here, the background CO value (400 ppb) was defined as the lowest 1.25th percentile of CO values during the campaign (Kondo et al., 2006). Figure 8 shows that the ratios of Abs370,BrC,sec/ΔCO increased with both aqSOA concentration and ALWC from 17:00 to 03:00 LT (r2=0.63, 0.57, p<0.001), whereas Abs370,BrC,pri/ΔCO decreased slightly with increasing BBOA and m/z 60 concentrations over the same period (r2=0.35, 0.33, p<0.001). Additionally, the average concentrations of NO3, NH4, and NO2 from 17:00 to 03:00 LT (9.1 µg m−3, 5.6 µg m−3, and 16.0 ppb, respectively) were 1.2, 1.2, and 1.3 times those from 04:00 to 16:00 LT (7.7 µg m−3, 4.7 µg m−3, and 12.6 ppb, respectively). These results are consistent with previous winter observations in the SCB (Peng et al., 2025; Wu et al., 2024).
As discussed in Sect. 3.2, SOA with hydroxyl groups, such as glyoxal and methylglyoxal, can form from aged BBOA through aqueous-phase reactions under high ALWC. Previous studies have shown that oligomers formed through aqueous reactions of glyoxal with NH3, which contain C = C or C = N bonds, exhibit strong absorption in near-UV regions (Laskin et al., 2015; Lee et al., 2013; Nozière et al., 2009; Powelsonet al., 2014). This suggested that secondary BrC chromophores with strong absorption at 370 nm were formed under high ALWC from 17:00 to 03:00 LT, which may be related to aqSOA generated from aged BBOA through aqueous-phase reactions. The low values of Abs370,BrC,sec/ΔCO from 12:00 and 14:00 LT may be related to photolysis and/or photooxidation causing BrC photobleaching (Sareen et al., 2013; Zhao et al., 2015). Overall, our findings suggest that aqSOA formed from biomass-burning emissions contributed significantly to BrC absorption, especially at night during the campaign.
Relationship between (a) AAE370–880 and the mass fraction of aqSOA (faqSOA= aqSOA/OA), coloured by the mass fraction of BBOA (fBBOA= BBOA/OA), and (b) BC-to-OA ratios coloured by faqSOA. (c) Variations of fBBOA as a function of AAE370–880. The red curve in (b) was the best fit curve to data taken from Lu et al. (2015) and described the Abs of fresh and aged BBOA.
Previous studies indicate that biomass-burning activity is negligible in summer, and although it may also occur in spring and winter, its intensity is typically lower than in autumn (Chen et al., 2014, 2017; Tao et al., 2014; Yang et al., 2019). Tao et al. (2014) reported that biomass burning contributed 19 ± 11 % to PM2.5 during autumn, significantly higher than in other seasons, and accounted for the highest fraction of organic matter in PM2.5. Additionally, the concentration of BBOA and its fraction in OA during autumn in this study (8.6 ± 7.7 µg m−3 and 34.8 ± 11.2 %, respectively) were respectively higher than those observed during summer (0.41 µg m−3 and 5.7 %, respectively) (Zeng et al., 2025) and winter in the SCB (Tang et al., 2025; Zhang et al., 2023) (Table S1). Notably, the ALWC during autumn in this study (41.6 ± 24.9 µg m−3) was substantially higher than that reported for summer (18.6 ± 35.3 µg m−3; Zeng et al., 2025) and winter (27.4 ± 9.7 µg m−3; Tang et al., 2025) in the SCB. Wang et al. (2018) observed that RH values at Chengdu and Chongqing in autumn were also higher than those in other seasons. Previous research indicates that, while aqueous-chemistry pathways in spring were comparable to those in autumn, photochemical bleaching of BrC was potentially stronger in spring (Wang et al., 2019a). Although winter features lower biomass-burning emissions, secondary BrC could still form from BBOA through aqueous-phase reactions under high NOx and NH4 concentrations and stagnant nighttime conditions, as observed during winter in the SCB (Peng et al., 2025; Wu et al., 2024). In summer, elevated temperature and Ox (Ox= NO2+ O3) levels could enhance photochemical oxidation, promoting secondary BrC formation while also intensifying BrC photobleaching (Wu et al., 2024). In summary, while secondary BrC can derive from BBOA through aqueous-phase reactions in all seasons in the SCB (with the possible exception of spring), the elevated ALWC and BBOA concentrations during autumn are favourable for its aqueous-phase formation.
AAE370–880 is another key parameter for characterizing aerosol absorption properties. Figure 9 displays its correlations with the mass fraction of aqSOA (faqSOA) and BBOA (fBBOA) to OA and the BC-to-OA ratio. During the campaign, a strong positive correlation (r2=0.49, p<0.001) was observed between AAE370–880 and faqSOA, with AAE370–880 reaching values up to 2.65. In contrast, AAE370–880 increased only slightly with increasing fBBOA (r2=0.21, p<0.001) (Fig. 9a, c). AAE was calculated using a power-law fitting of aerosol absorption values (Qin et al., 2018; Wang et al., 2019b). While BC concentration was linearly dependent on AbsBC, OA concentration did not follow the same pattern with AbsBrC. The mixing state of BC and OA, influenced by combustion conditions, can also affect AAE. Previous studies have shown that biomass-burning emissions can impact absorption properties, which is reflected in the relationship between AAE and the BC-to-OA ratio (a measure of the combustion conditions) (Lu et al., 2015; Saleh et al., 2014). Thus, the relationship observed in Fig. 9b reflects the influence of biomass-burning emissions during this campaign. The parameterised curve (black) agrees with prior research (red) for wavelengths from 370 to 880 nm (Lu et al., 2015). When 950 nm was used as the highest wavelength instead of 880 nm, AAE370–950 values differed by less than 10 % from AAE370–880. Notably, data points with high AAE370–880 corresponded to low BC-to-OA ratios and large faqSOA values. Moreover, the average value of AAE370–880 observed in this study (1.95) was higher than AAE370–950 observed in the laboratory experiments on fresh and photochemically aged biomass-burning emissions (i.e., 1.38 and 1.48 for fresh oak and pocosin pine, and 1.42 and 1.73 for aged oak and pocosin pine) (Saleh et al., 2013).
Conclusions
This study conducted comprehensive real-time measurements of the light absorption properties and chemical composition of carbonaceous aerosols during autumn in the Sichuan Basin, China. The findings demonstrated that aqueous secondary organic aerosol (aqSOA) formed from aged biomass-burning emissions under high aerosol liquid water content (ALWC >60µg m−3) conditions significantly contributes to aerosol pollution and light absorption. OA was the dominant component of PM2.5 (46.6 ± 10.7 %) and exhibited strong absorption at UV wavelengths (Abs370,BrC=42.4± 28.5 Mm−1). During PP, aqSOA contributed, on average, 14.1 % to OA (7.6 µg m−3), exhibiting enhanced oxidation (f29=0.141± 0.062, f44=0.080±0.035) and substantial light absorption characteristics (Abs370,BrC=91.6 Mm−1, AAE370–880=2.1). Additionally, less-oxidized aqSOA, formed predominantly through aqueous-phase reactions, instead of gas-phase photochemical oxidation of their precursors, significantly contributed to the dynamic evolution of haze pollution during PP. Backward trajectory analysis further revealed that regionally transported BBOA, which originated primarily from northeastern Chongqing, underwent aqueous-phase aging to aqSOA within approximately 12–48 h. These results underscore that aqueous-phase reactions of BBOA – particularly during the transport of biomass-burning plumes – convert primary emissions into strongly light-absorbing aqSOA, thereby substantially influencing regional haze formation and radiative forcing.
Our findings align with previous laboratory studies on biomass-burning BrC formation, and provide novel ambient quantification of these processes under realistic atmospheric conditions. The parameterized curve of AAE370–880 versus BC-to-OA ratios in this study was consistent with previous laboratory research on biomass-burning emissions. The mean AAE370–880 observed in this study (1.95) was higher than the values reported for fresh and photochemically aged biomass-burning emissions in laboratory experiments, and increased significantly with increasing faqSOA (r2=0.49, p<0.001). Additionally, elevated Abs370,BrC,sec values coincided with high ALWC, NO3, and NH4 levels and correlated strongly with aqSOA concentration (r2=0.44, p<0.001). These results suggest that aqueous-phase reactions of BBOA under high-NOx and high-NH4 conditions produce secondary BrC with particularly strong light absorption. Notably, seasonal variations in biomass-burning emissions and the associated chemical processing of carbonaceous aerosols must be adequately represented in climate and air quality models. Conducting the campaign in autumn, when biomass-burning activity is intense, is critical to avoid underestimating aerosol impacts in this season and overestimating them in other seasons. However, the results may not fully represent aerosol processes in other seasons. The relative uncertainty of AbsBrC at 370 nm, resulting from the choice of AAEBC, ranged from -112% to 42 %. Nevertheless, our results underscore the importance of aqueous-phase processing in transforming biomass-burning emissions, with important implications for climate and air quality modelling. The substantial contribution of aqSOA to aerosol mass and light absorption highlights the requirement for improved representation of aqueous processes in models. The linkages established here among aging timescales, transport pathways, and aqSOA formation provide a transferable framework for understanding aqSOA processing in other humid regions influenced by biomass burning. Research on BrC chromophores is still in its early stages, and quantitative linking their chemical composition and light absorption properties to biomass-burning emissions across different seasons are necessary to improve our understanding of their climatic and environmental effects. Future research should prioritize molecular-level characterization of aqSOA precursors and products, quantification of aqueous reaction rates under ambient conditions, and multi-scale modelling to assess regional climate impacts. This study highlights that aqueous processes play an important role in the evolution of biomass-burning emissions and should be adequately considered in both air quality budgets and climate forcing balance on a global scale.
Data availability
The data generated and analysed in this study are available from 10.5281/zenodo.18635386 (Peng et al., 2026).
The supplement related to this article is available online at https://doi.org/10.5194/acp-26-4131-2026-supplement.
Author contributions
CZ, CP, YD, and ZL designed the experiments. Data analysis and interpretation were performed by CP, ZT, HT, KZ, ZL, and GS. CP, XY, and MT wrote the paper. ZT, YC, XL, LZ, YC, and YF contributed to the paper with useful scientific discussions or comments.
Competing interests
The contact author has declared that none of the authors has any competing interests.
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Acknowledgements
Thanks for the data contributed by the field campaign team.
Financial support
This research has been supported by the Natural Science Foundation of Chongqing Municipality (grant no. CSTB2022NSCQ-MSX0504), the National Natural Science Foundation of China (grant no. 42305126), and the National Key Research and Development Program of China (grant no. 2023YFC3709301).
Review statement
This paper was edited by Barbara Ervens and reviewed by two anonymous referees.
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