Comment on acp-2021-729

Abstract. The predominating role of aerosol Fuchs surface area, AFuchs, in determining the occurrence of new particle formation (NPF) events in Beijing was elucidated in this study. The analysis was based on a field campaign from 12 March to 6 April 2016 in Beijing, during which aerosol size distributions down to ∼ 1 nm and sulfuric acid concentrations were simultaneously monitored. The 26 days were classified into 11 typical NPF days, 2 undefined days, and 13 non-event days. A dimensionless factor, LΓ, characterized by the relative ratio of the coagulation scavenging rate over the condensational growth rate (Kuang et al., 2010), was applied in this work to reveal the governing factors for NPF events in Beijing. The three parameters determining LΓ are sulfuric acid concentration, the growth enhancement factor characterized by contribution of other gaseous precursors to particle growth, Γ, and AFuchs. Different from other atmospheric environments, such as in Boulder and Hyytiälä, the daily-maximum sulfuric acid concentration and Γ in Beijing varied in a narrow range with geometric standard deviations of 1.40 and 1.31, respectively. A positive correlation between the estimated new particle formation rate, J1.5, and sulfuric acid concentration was found with a mean fitted exponent of 2.4. However, the maximum sulfuric acid concentrations on NPF days were not significantly higher (even lower, sometimes) than those on non-event days, indicating that the abundance of sulfuric acid in Beijing was high enough to initiate nucleation, but may not necessarily lead to NPF events. Instead, AFuchs in Beijing varied greatly among days with a geometric standard deviation of 2.56, whereas the variabilities of AFuchs in Tecamac, Atlanta, and Boulder were reported to be much smaller. In addition, there was a good correlation between AFuchs and LΓ in Beijing (R2 = 0.88). Therefore, it was AFuchs that fundamentally determined the occurrence of NPF events. Among 11 observed NPF events, 10 events occurred when AFuchs was smaller than 200 µm2 cm−3. NPF events were suppressed due to the coagulation scavenging when AFuchs was greater than 200 µm2 cm−3. Measured AFuchs in Beijing had a good correlation with its PM2.5 mass concentration (R2 = 0.85) since AFuchs in Beijing was mainly determined by particles in the size range of 50–500 nm that also contribute to the PM2.5 mass concentration.

<strong class="journal-contentHeaderColor">Abstract.</strong> Understanding chemical processes leading to the formation of atmospheric aerosol particles is crucial to improve our capabilities in predicting the future climate. However, those mechanisms are still inadequately characterized, especially in polar regions. In this study, we report observations of neutral and charged aerosol precursor molecules and chemical cluster composition (qualitatively and quantitatively), as well as air ions and aerosol particle number concentrations and size distributions from the Marambio research station (64<span class="inline-formula">^∘</span>15<span class="inline-formula">^′</span> S, 56<span class="inline-formula">^∘</span>38<span class="inline-formula">^′</span> W), located north of the Antarctic Peninsula. We conducted measurements during the austral summer, between 15 January and 25 February 2018. The scope of this study is to characterize new particle formation (NPF) event parameters and connect our observations of gas-phase compounds with the formation of secondary aerosols to resolve the nucleation mechanisms at the molecular scale. NPF occurred on 40 % of measurement days. All NPF events were observed during days with high solar radiation, mostly with above-freezing temperatures and with low relative humidity. The averaged formation rate for 3 nm particles (<span class="inline-formula"><i>J</i>₃</span>) was 0.686 cm<span class="inline-formula">^−3</span> s<span class="inline-formula">^−1</span>, and the average particle growth rate (GR<span class="inline-formula">_{3.8–12 nm}</span>) was 4.2 nm h<span class="inline-formula">^−1</span>. Analysis of neutral aerosol precursor molecules showed measurable concentrations of iodic acid (IA), sulfuric acid (SA), and methane sulfonic acid (MSA) throughout the entire measurement period with significant increase in MSA and SA concentrations during NPF events. We highlight SA as a key contributor to NPF processes, while IA and MSA likely only contribute to particle growth. Mechanistically, anion clusters containing ammonia and/or dimethylamine (DMA) and SA were identified, suggesting significant concentration of ammonia and DMA as well. Those species are likely contributing to NPF events since SA alone is not sufficient to explain observed nucleation rates. Here, we provide evidence of the marine origin of the measured chemical precursors and discuss their potential contribution to the aerosol phase.

Aerosol size distribution and new particle formation events in the suburb of Xi'an, northwest China

&amp;lt;p&amp;gt;The Cloud Condensation Nuclei (CCN) budget, the aerosol particles population that could become cloud droplets, can be influenced by primary aerosol particles emitted by different sources (anthropogenic or biogenic) or by secondary particles that have undergone growth processes or chemical transformations. Aerosol particles originated by nucleation of precursor gases in the atmosphere have been identified as an important source of CCN particles. The influence of New Particle Formation (NPF) events to CCN concentrations is highly dependent on the environment where it takes place. Specifically, the study of the influence of NPF events on CCN concentration at high-altitude sites, where atmospheric conditions favor the formation of clouds, is a very interesting scientific goal.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;&amp;amp;#160;&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;This study presents CCN measurements combined with aerosol size distribution at a high-altitude station in the South East of Spain: a remote high mountain site (Sierra Nevada; SNS, 2500 m a.s.l.). Due to its high altitude, the aerosol particles over SNS station are often representative of pristine free troposphere conditions, especially in winter and nighttime. During summer, SNS station is frequently influenced by transport of pollutants from Granada city to Sierra Nevada station as a result of mixing layer growth and the activation of the mountain-valley breeze phenomenon as well as by NPF events at midday (De Arruda Moreira et al., 2019; Casquero-Vera et al., 2020).&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;&amp;amp;#160;&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;In this study, we analyze the influence of NPF events to CCN concentrations during summer 2019 at the SNS high-altitude station. The study period (from June to August of 2019) was characterized by 67 NPF events, 16 undefined events and 13 non-events days. Following Rose et al. (2017) criteria, only those NPF events referred as type I, i.e. with clear particle growth from smallest sizes, were selected to investigate the contribution of NPF events on CCN concentrations. In this sense, we selected the 15 clearest NPF events for this analysis.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;&amp;amp;#160;&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Results show clear differences in the diurnal evolution of CCN concentration between NPF event and non-event days, demonstrating the large influence of NPF to CCN concentrations, especially at high supersaturations (Rejano et al., 2021). NPF events have been estimated to increase the CCN concentrations by 175% at SS=0.5%, evidencing NPF events as one of the major CCN source at this mountain site&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;&amp;amp;#160;&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;&amp;amp;#160;&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;&amp;lt;strong&amp;gt;Acknowledgments&amp;lt;/strong&amp;gt;: This work was supported by the European Union's Horizon 2020 research and innovation programme through project ACTRIS 2 (grant agreement No 654109), by the Spanish Ministry of Economy and Competitiveness through projects CGL2016-81092-R, CGL2017-90884-REDT and RTI2018-101154-A-I00 and by University of Granada Plan Propio through Visiting Scholars program. The Spanish Ministry of Universities funds Fernando Rejano under the predoctoral program FPU (FPU19/05340).&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;&amp;amp;#160;&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;&amp;lt;strong&amp;gt;References&amp;lt;/strong&amp;gt;&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Casquero-Vera, et al. (2020) Atmos. Chem. Phys. &amp;lt;strong&amp;gt;20, &amp;lt;/strong&amp;gt;14253&amp;amp;#8211;14271.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;De Arruda Moreira et al. (2019) Atmos. Chem. Phys. &amp;lt;strong&amp;gt;19&amp;lt;/strong&amp;gt;, 1263-1280.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Rejano et al. (2021) Sci. Tot Envi., &amp;lt;strong&amp;gt;762&amp;lt;/strong&amp;gt;, 143100.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Rose et al. (2017) Atmos. Chem. Phys. &amp;lt;strong&amp;gt;17&amp;lt;/strong&amp;gt;, 1529-1541.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;tract HTML here.&amp;lt;/p&amp;gt;

Abstract. New particle formation (NPF) and growth are a major source of atmospheric fine particles. In polluted urban environments, NPF events are frequently observed with characteristics distinct from those in clean environments. Here we simulate NPF events in urban Beijing with a discrete-sectional model that couples cluster dynamics and multicomponent particle growth. In the model, new particles are formed by sulfuric acid–dimethylamine nucleation, while particle growth is driven by particle coagulation and the condensation of sulfuric acid, its clusters, and oxygenated organic molecules (OOMs). A variable simulation domain in the particle size space is applied to isolate newly formed particles from preexisting ones, which allows us to focus on new particle formation and growth rather than the evolution of particles of non-NPF origin. The simulation yields a rich set of information including the time-dependent NPF rates, the cluster concentrations, the particle size distributions, and the time- and size-specific particle chemical compositions. These can be compared with the field observations to comprehensively assess the simulation–observation agreement. Sensitivity analysis with the model further quantifies how metrics of NPF events (e.g., particle survival probability) respond to model input variations and serves as a diagnostic tool to pinpoint the key parameter that leads to simulation–observation discrepancies. Seven typical NPF events in urban Beijing were analyzed. We found that with the observed gaseous precursor concentrations and coagulation sink as model inputs, the simulations roughly captured the evolution of the observed particle size distributions; however, the simulated particle growth rate was insufficient to yield the observed particle number concentrations, survival probability, and mode diameter. With the aid of sensitivity analysis, we identified under-detected OOMs as a likely cause for the discrepancy, and the agreement between the simulation and the observation was improved after we modulated particle growth rates in the simulation by adjusting the abundance of OOMs.

The formation of new atmospheric aerosol particles and their subsequent growth have been observed under different environmental conditions globally; such observations are few over northwest China. Here, we present an analysis of some case studies for new particle formation (NPF) events from two distinct suburban locations in northern China during May and June of two consecutive years, and provide more information to understand the characteristics of NPF events in North China. Particle number size distribution was measured at suburbs of Beijing (39.75° N, 116.96° E) during 1 June to 2 July 2013 and at suburbs of Xi’an (34.09° N, 108.55° E) during 1 to 25 May 2014. The average of total particle number concentration in the similar size range of 10–487 nm at the suburbs of Beijing (9.0 × 103 cm−3) was about two times higher than those observed at Xi’an (4.7 × 103 cm−3), and the mean particle mode diameter at Beijing was 1.4-fold higher than that at Xi’an. The estimated total condensation sink (CS) at Beijing (3.11 × 10−2 s−1) was also higher than at Xi’an (1.13 × 10−2 s−1). The frequency of NPF events at suburb of Beijing was 24%, lower than that in Xi’an (50%), and also lower than urban site of Beijing (35% in June) and another suburb of Beijing (over 50% in June). The NPF events with (Class I) or without (Class II) subsequent growth were both observed at the two suburb sites. The derived GR at the suburb of Beijing (range from 4.6 to 8.6 nm h−1) was a little higher than that at Xi’an (range from 3.3 to 6.7 nm h−1), which are generally comparable to typical values in mid-latitude reported in previous studies. The air masses coming from north or northwest China favor the occurrence of NPF event under low condensation sink and clear days. The number size distributions of freshly nucleated particles showed clear bimodal distributions on both sites. Additionally, Mode Dp of nucleated particles at the two sites was 17 ± 1 nm and 22 ± 4 nm, respectively during the periods with NPF events. The case study of NPF events at the two suburb sites shows that the surface area concentration and total scattering coefficient (SC) was significant decreased during the NPF events at both sites. High temperature, low condensation sink and low relative humidity furthered the occurrence of NPF events, and wind direction shifts were important for the subsequent growth of particles. NPF events in the suburbs of Beijing usually occurred when relative humidity (RH) &lt; 55%, CS &lt; 0.02 s−1, or 55% &lt; RH &lt; 68%, CS &lt; 0.01 s−1. However, there is no clear range for Xi’an. Furthermore, we observed that some NPF events occurred at higher RH and very low CS in this study on both sites, which means that low CS may be more important than low RH for the particle formation on clear days.

New particle formation (NPF) in the atmosphere i.e. nucleation of gas phase precursors and continuing condensa- tional growth is a crucial secondary transformation process. The freshly nucleated particles can grow into sizes where they can act as cloud condensation nuclei (CCN) and further influence cloud and climate-relevant properties. Hence, the detailed knowledge on the formation mechanisms of new particles and their subsequent growth will help us to improve our under- standing on the regional air pollution and global climate change. Recent-developed measurement techniques enable to ex- plore atmospheric nucleation by measuring particles/clusters down to 1 nm. NPF events have been observed in a variety of atmospheric environments. Several methods including field observation, laboratory simulations and model calculations are implemented to investigate the nucleation mechanisms and growth properties. Good agreement between particle formation rates and gaseous sulfuric acid concentrations is observed, indicating that sulfuric acid is a key compnent in the atmospheric nucleation process. In addition, the low-volatile organic vapors are found to be involved in new particle formation. However, the huge variations of the particle formation and growth rates in diverse atmospheric environments suggest that a consistent picture on formation mechanisms of new particles does not achieve. Long-term continuous measurements of NPF events have been first performed in the urban atmosphere of Beijing since 2004. Up to now, NPF events have been observed in many different environments, including coastal area, high-elevation mountain, rural site as well as urban region in China. The cur- rent nucleation mechanisms are developed based on the observation in clean environment. Hence, whether it could well ex- plain the NPF events occurred in the polluted atmosphere with strong oxidation capacity is a key issue to be addressed in further studies. This paper reviews the measurement techniques for investigating atmospheric new particle formation and growth, summarizes the observation results in various typical environments, introduces the current understanding of the nu- cleation mechanisms and discusses the main scientific questions that need further researches. Keywords new particle formation; nucleation mechanism; growth property; measurement technique; precursor 1 引言

We present a supervised machine learning (ML) framework to automatically identify new particle formation (NPF) events and analyze key atmospheric factors associated with their occurrence and growth. We applied ML to detect NPF events using start time and particle concentrations across size ranges, while identifying atmospheric variables including ambient temperature, relative humidity, solar radiation intensity (SRI), wind speed, wind direction, boundary layer height, total organics, sulfate, nitrate, total surface area concentration, sulfur dioxide, and turbulent kinetic energy (TKE). We analyzed a 6‐year data set from the Atmospheric Radiation Measurement at the Southern Great Plains (SGP) site in Oklahoma, USA. Using long‐term ground‐based measurements, we identified NPF events and applied Random Forest Classifiers, which achieved 90%–95% prediction accuracy. Feature importance analysis highlighted SRI, relative humidity, and ambient temperature as the most influential variables, contributing normalized importances of 28%, 17%, and 10%. Partial Dependence Plots (PDPs) indicated that higher SRI and lower relative humidity were critical in promoting NPF formation at SGP. Seasonally, NPF events were more frequent in winter (42.1%) and spring (35.5%), and least in summer (4.0%). Particle growth rates also exhibited a seasonal variation, with the lowest in winter (below 2 nm hr −1 ) and highest in late spring and early summer (exceeding 5 nm hr −1 ). Temperature, turbulent kinetic energy, and aerosol properties were the primary factors of growth rate variability. This study advances predictive modeling of NPF, offers insights for future campaign deployments, and demonstrates the effectiveness of ML in understanding the formation and growth of atmospheric aerosols.

Formation of Ultrafine particles (UFPs) in the urban atmosphere is expected to be less favored than in the rural atmosphere due to the high existing particle surface area acting as a sink for newly-formed particles Despite the large condensation sink (CS) values, previous comparative studies between rural and urban site reported higher frequency of new particle formation (NPF) events over urban sites in comparison to background sites as well as higher particle formation and growth rates attributed to the higher concentration of condensable species. The present study aims to better understand the environmental factors favoring, or disfavoring, atmospheric NPF over Lille, a large city North of France and to analyze their impact on particle number concentration using a long-term dataset (4 years : 1st July 2017 to 31st December 2020). The results highlight a strong seasonal variation of the NPF occurrences with a maximum observed during spring (27 events) and summer (53 events). It was found that high temperature (T > 295 K), low RH (RH < 45 %) and high solar radiation are ideal to observe NPF events over Lille. Relatively high values of condensation sink (CS ~ 2.10-2 s-1) are reported during event days suggesting that high CS does not inhibit the occurrence of NPFt over our site. Moreover, the particle Growth Rate (GR15.7-30 nm) was positively correlated with the temperature most probably linked to the higher emissions of precursors. Finally, the nucleation strength factor (NSF) was calculated to highlight the impact of those NPF events on particle number concentrations. NSF15.7-100 reaches a maximum of 4 in summer, indicating an enormous contribution of NPF events to particle number concentration at this time of the year.

In urban and remote atmospheres, new particle formation (NPF) events often occur after dust storms, which can have further impacts on regional and global climate. Additionally, the levels of gaseous precursors and condensation sink (CS) resulting from anthropogenic emissions can also influence the occurrence and intensity of NPF events. Over the past decade, China has implemented various air quality improvement actions, leading to significant changes in air pollutant emissions. However, there have been limited studies on the long-term evolution of NPF events caused by the synergy of dust storms and anthropogenic emissions. This study aims to analyze the characteristics of dust-related NPF events in Beijing from 2009 to 2017 and compare them with non-dust NPF events. The results show that the formation rates of dust-related NPF events decreased due to the reduction of SO2 emissions. However, the growth rates remained stable, possibly due to the increasing oxidation capacity in Beijing. These findings contribute to a deeper understanding of the climate effects of natural dust under the influence of anthropogenic emission control measures.

Abstract. Understanding the particle number size distributions in diversified atmospheric environments is important in order to design mitigation strategies related to submicron particles and their effects on regional air quality, haze and human health. In this study, we conducted 15 different field measurement campaigns between 2007 and 2011 at 13 individual sites in China, including five urban sites, four regional sites, three coastal/background sites and one ship cruise measurement along eastern coastline of China. Size resolved particles were measured in the 15–600 nm size range. The median particle number concentrations (PNCs) were found to vary in the range of 1.1−2.2 × 104 cm−3 at urban sites, 0.8−1.5 × 104 cm−3 at regional sites, 0.4−0.6 × 104 cm−3 at coastal/background sites, and 0.5 × 104 cm−3 during cruise measurement. Peak diameters at each of these sites varied greatly from 24 to 115 nm. Particles in the 15–25 nm (nucleation mode), 25–100 nm (Aitken mode) and 100–600 nm (accumulation mode) range showed different characteristics at each sites, indicating the features of primary emissions and secondary formation in these diversified atmospheric environments. Diurnal variations show a build-up of accumulation mode particles belt at regional sites, suggesting the contribution of regional secondary aerosol pollution. Frequencies of new particle formation (NPF) events were much higher at urban and regional sites than at coastal sites and during cruise measurement. The average growth rates (GRs) of nucleation mode particles were 8.0–10.9 nm h−1 at urban sites, 7.4–13.6 nm h−1 at regional sites and 2.8–7.5 nm h−1 at coastal sites and during cruise measurement. The high gaseous precursors and strong oxidation at urban and regional sites not only favored the formation of particles, but also accelerated the growth rate of the nucleation mode particles. No significant difference in condensation sink (CS) during NPF days were observed among different site types, suggesting that the NPF events in background areas were more influenced by the pollutant transport. In addition, average contributions of NPF events to potential cloud condensation nuclei (CCN) at 0.2% super-saturation in the afternoon of all sampling days were calculated as 11% and 6% at urban sites and regional sites, respectively. On the other hand, NPF events at coastal sites and during cruise measurement had little impact on potential production of CCN. This study provides a large data set of particle size distribution in diversified atmosphere of China, improving our general understanding of emission, secondary formation, new particle formation and corresponding CCN activity of submicron aerosols in Chinese environments.

The aerosol number spectrum and gas pollutants were measured and the new particle formation (NPF) events were discussed in Nanjing. The results showed that the size distributions of aerosol number concentrations exhibited distinct seasonal variations, implying the relations of particle sizes and their sources and sinks. The number concentrations of particles in the nuclei mode (10–30 nm), Aitken mode (30–100 nm), accumulation mode (100–1000 nm) and coarse mode (>1 μm) varied in the order of summer > spring > autumn, summer > autumn > spring, autumn > summer > spring, and spring > autumn >summer, respectively. The diurnal variation of total aerosol number concentrations showed three peaks in all observed periods, which corresponded to two rush hours and the photochemistry period at noon. In general, the NPF in summer occurred under the conditions of east winds and dominant air masses originating from marine areas with high relative humidity (50%–70%) and strong solar radiations (400–700 W m−2). In spring, the NPF were generally accompanied by low relative humidity (14%–30%) and strong solar radiations (400–600 W m−2). The new particle growth rates (GR) were higher in the summertime in the range of 10–16 nm h−1. In spring, the GR were 6.8–8.3 nm h−1. Under polluted air conditions, NPF events were seldom captured in autumn in Nanjing. During NPF periods, positive correlations between 10–30 nm particles and O3 were detected, particularly in spring, indicating that NPF can be attributed to photochemical reactions.

Significant effects of transport on nanoparticles during new particle formation events in the atmosphere of Beijing

Abstract. In this study, we investigate atmospheric new particle formation (NPF) across 65 d in the Bolivian central Andes at two locations: the mountaintop Chacaltaya station (CHC, 5.2 km above sea level) and an urban site in El Alto–La Paz (EAC), 19 km apart and at 1.1 km lower altitude. We classified the days into four categories based on the intensity of NPF, determined by the daily maximum concentration of 4–7 nm particles: (1) high at both sites, (2) medium at both, (3) high at EAC but low at CHC, and (4) low at both. These categories were then named after their emergent and most prominent characteristics: (1) Intense-NPF, (2) Polluted, (3) Volcanic, and (4) Cloudy. This classification was premised on the assumption that similar NPF intensities imply similar atmospheric processes. Our findings show significant differences across the categories in terms of particle size and volume, sulfuric acid concentration, aerosol compositions, pollution levels, meteorological conditions, and air mass origins. Specifically, intense NPF events (1) increased Aitken mode particle concentrations (14–100 nm) significantly on 28 % of the days when air masses passed over the Altiplano. At CHC, larger Aitken mode particle concentrations (40–100 nm) increased from 1.1 × 103 cm−3 (background) to 6.2 × 103 cm−3, and this is very likely linked to the ongoing NPF process. High pollution levels from urban emissions on 24 % of the days (2) were found to interrupt particle growth at CHC and diminish nucleation at EAC. Meanwhile, on 14 % of the days, high concentrations of sulfate and large particle volumes (3) were observed, correlating with significant influences from air masses originating from the actively degassing Sabancaya volcano and a depletion of positive 2–4 nm ions at CHC but not at EAC. During these days, reduced NPF intensity was observed at CHC but not at EAC. Lastly, on 34 % of the days, overcast conditions (4) were associated with low formation rates and air masses originating from the lowlands east of the stations. In all cases, event initiation (∼ 09:00 LT) generally occurred about half an hour earlier at CHC than at EAC and was likely modulated by the daily solar cycle. CHC at dawn is in an air mass representative of the regional residual layer with minimal local surface influence due to the barren landscape. As the day progresses, upslope winds bring in air masses affected by surface emissions from lower altitudes, which may include anthropogenic or biogenic sources. This influence likely develops gradually, eventually creating the right conditions for an NPF event to start. At EAC, the start of NPF was linked to the rapid growth of the boundary layer, which favored the entrainment of air masses from above. The study highlights the role of NPF in modifying atmospheric particles and underscores the varying impacts of urban versus mountain top environments on particle formation processes in the Andean region.

A significant fraction (&gt;50%) of current cloud condensation nuclei (CCN) is estimated to stem from the formation of new particles. But the mechanisms governing new particle formation (NPF) process are still poorly understood, especially regarding preindustrial NPF. In order to investigate preindustrial NPF process and its contribution to CCN budget, intensive ambient observations were carried out between March 28 and June 27, 2022 at the pristine high-altitude Iza&amp;#241;a Atmospheric Observatory (IZO; 2367 m a.s.l., 28&amp;#176;18'32.3"N 16&amp;#176;29'58.1"W), which is located on the island of Tenerife, Canary Islands. This site is characterized by clean air and pristine skies with minimal local anthropogenic influence. Among with other instrumentations, a Multi-scheme chemical IONization (MION) inlet coupled to an atmospheric pressure interface time-of-flight mass spectrometer (APi-ToF-MS) was used to measure the molecular composition of neutral vapours including the less oxygenated organic compounds, sulphuric acid (SA), methane sulfonic acid (MSA), and highly oxygenated organic molecules (HOM) via the fast switching of two reagent ion schemes (Br- and NO3-). A Vocus proton-transfer-reaction time-of-flight mass spectrometer (PTR-ToF) was deployed to measure the potential precursor volatile organic compounds (VOC), dimethylsulphide (DMS) and their oxidation products. Filter samples were collected and analyzed in the laboratory with a filter inlet for gases and aerosols coupled to a high-resolution time-of-flight chemical ionization mass spectrometer (FIGAERO-HR-TOF-CIMS), yielding the molecular composition of particulate organics. During the measurement period, clustering events were frequently observed, particularly in May and June. NPF precursors, e.g., SA and HOM, were also substantially higher in May and June, indicating their potential role in the NPF process. This is also consistent with the time series of their precursors such as DMS, SO2, and terpenes. NPF events in the presence of Sahara dust events were also observed, exhibiting lower levels of organics in the particle phase compared to clear NPF events. In addition, higher levels of marine MSA and SA were observed on some nights, potentially resulting from the updraft and transport from the Atlantic Ocean to the marine free troposphere. The measurements at IZO station provide us with a valuable dataset regarding NPF at this pristine high-altitude location with marine and Sahara dust influences. Chemical characterization of the freshly formed clusters will increase our understanding of the nucleation mechanism responsible for preindustrial NPF, as well as free tropospheric chemistry. Our study will also provide new insights on a molecular basis to better understand present and future aerosols, and their effects on air quality and climate.