Artículos de revistas sobre el tema "Aerosol origins"
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1
EVERTS, SARAH. "AEROSOL ORIGINS". Chemical & Engineering News 85, n.º 10 (5 de marzo de 2007): 10. http://dx.doi.org/10.1021/cen-v085n010.p010a.
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Song, Congbo, Manuel Dall'Osto, Angelo Lupi, Mauro Mazzola, Rita Traversi, Silvia Becagli, Stefania Gilardoni et al. "Differentiation of coarse-mode anthropogenic, marine and dust particles in the High Arctic islands of Svalbard". Atmospheric Chemistry and Physics 21, n.º 14 (28 de julio de 2021): 11317–35. http://dx.doi.org/10.5194/acp-21-11317-2021.
Resumen
Abstract. Understanding aerosol–cloud–climate interactions in the Arctic is key to predicting the climate in this rapidly changing region. Whilst many studies have focused on submicrometer aerosol (diameter less than 1 µm), relatively little is known about the supermicrometer aerosol (diameter above 1 µm). Here, we present a cluster analysis of multiyear (2015–2019) aerodynamic volume size distributions, with diameter ranging from 0.5 to 20 µm, measured continuously at the Gruvebadet Observatory in the Svalbard archipelago. Together with aerosol chemical composition data from several online and offline measurements, we apportioned the occurrence of the coarse-mode aerosols during the study period (mainly from March to October) to anthropogenic (two sources, 27 %) and natural (three sources, 73 %) origins. Specifically, two clusters are related to Arctic haze with high levels of black carbon, sulfate and accumulation mode (0.1–1 µm) aerosol. The first cluster (9 %) is attributed to ammonium sulfate-rich Arctic haze particles, whereas the second one (18 %) is attributed to larger-mode aerosol mixed with sea salt. The three natural aerosol clusters were open-ocean sea spray aerosol (34 %), mineral dust (7 %) and an unidentified source of sea spray-related aerosol (32 %). The results suggest that sea-spray-related aerosol in polar regions may be more complex than previously thought due to short- and long-distance origins and mixtures with Arctic haze, biogenic and likely blowing snow aerosols. Studying supermicrometer natural aerosol in the Arctic is imperative for understanding the impacts of changing natural processes on Arctic aerosol.
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Xia, Junji, Fengrong Zhu, Xingbing Zhao, Jing Liu, Hu Liu, Guotao Yuan, Qinning Sun et al. "Optical Properties and Possible Origins of Atmospheric Aerosols over LHAASO in the Eastern Margin of the Tibetan Plateau". Remote Sensing 16, n.º 10 (10 de mayo de 2024): 1695. http://dx.doi.org/10.3390/rs16101695.
Resumen
The accuracy of cosmic ray observations by the Large High Altitude Air Shower Observatory Wide Field-of-View Cherenkov/Fluorescence Telescope Array (LHAASO-WFCTA) is influenced by variations in aerosols in the atmosphere. The solar photometer (CE318-T) is extensively utilized within the Aerosol Robotic Network as a highly precise and reliable instrument for aerosol measurements. With this CE318-T 23, 254 sets of valid data samples over 394 days from October 2020 to October 2022 at the LHAASO site were obtained. Data analysis revealed that the baseline Aerosol Optical Depth (AOD) and Ångström Exponent (AE) at 440–870 nm (AE440–870nm) of the aerosols were calculated to be 0.03 and 1.07, respectively, suggesting that the LHAASO site is among the most pristine regions on Earth. The seasonality of the mean AOD is in the order of spring > summer > autumn = winter. The monthly average maximum of AOD440nm occurred in April (0.11 ± 0.05) and the minimum was in December (0.03 ± 0.01). The monthly average of AE440–870nm exhibited slight variations. The seasonal characterization of aerosol types indicated that background aerosol predominated in autumn and winter, which is the optimal period for the absolute calibration of the WFCTA. Additionally, the diurnal daytime variations of AOD and AE across the four seasons are presented. Our analysis also indicates that the potential origins of aerosol over the LHAASO in four seasons were different and the atmospheric aerosols with higher AOD probably originate mainly from Northern Myanmar and Northeast India regions. These results are presented for the first time, providing a detailed analysis of aerosol seasonality and origins, which have not been thoroughly documented before in this region, also enriching the valuable materials on aerosol observation in the Hengduan Mountains and Tibetan Plateau.
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Laskin, Alexander, Julia Laskin y Sergey A. Nizkorodov. "Mass spectrometric approaches for chemical characterisation of atmospheric aerosols: critical review of the most recent advances". Environmental Chemistry 9, n.º 3 (2012): 163. http://dx.doi.org/10.1071/en12052.
Resumen
Environmental contextAtmospheric aerosols have profound effects on the environment through several physicochemical processes, such as absorption and scattering of sunlight, heterogeneous gas–particle reactions and adverse effects on the respiratory and cardiovascular systems. Understanding aerosol atmospheric chemistry and its environmental impact requires comprehensive characterisation of the physical and chemical properties of particles. Results from mass spectrometry provide important new insights into the origin of atmospheric aerosols, the evolution of their physicochemical properties, their reactivity and their effect on the environment. AbstractThis manuscript presents an overview of the most recent instrument developments for the field and laboratory applications of mass spectrometry (MS) to investigate the chemistry and physics of atmospheric aerosols. A range of MS instruments, employing different sample introduction methods, ionisation and mass detection techniques are used both for ‘online’ and ‘offline’ characterisation of aerosols. Online MS techniques enable detection of individual particles with simultaneous measurement of particle size distributions and aerodynamic characteristics and are ideally suited for field studies that require high temporal resolution. Offline MS techniques provide a means for detailed molecular-level analysis of aerosol samples, which is essential to gain fundamental knowledge regarding aerosol chemistry, mechanisms of particle formation and atmospheric aging. Combined, complementary MS techniques provide comprehensive information on the chemical composition, size, morphology and phase of aerosols – data of key importance for evaluating hygroscopic and optical properties of particles, their health effects, understanding their origins and atmospheric evolution. Over the last few years, developments and applications of MS techniques in aerosol research have expanded remarkably as evident by skyrocketing publication statistics. The goal of this review is to present the most recent developments in the field of aerosol mass spectrometry for the time period of late 2010 to early 2012, which have not been conveyed in previous reviews.
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Hofer, Sabine, Norbert Hofstätter, Albert Duschl y Martin Himly. "SARS-CoV-2-Laden Respiratory Aerosol Deposition in the Lung Alveolar-Interstitial Region Is a Potential Risk Factor for Severe Disease: A Modeling Study". Journal of Personalized Medicine 11, n.º 5 (19 de mayo de 2021): 431. http://dx.doi.org/10.3390/jpm11050431.
Resumen
COVID-19, predominantly a mild disease, is associated with more severe clinical manifestation upon pulmonary involvement. Virion-laden aerosols and droplets target different anatomical sites for deposition. Compared to droplets, aerosols more readily advance into the peripheral lung. We performed in silico modeling to confirm the secondary pulmonary lobules as the primary site of disease initiation. By taking different anatomical aerosol origins into consideration and reflecting aerosols from exhalation maneuvers breathing and vocalization, the physicochemical properties of generated respiratory aerosol particles were defined upon conversion to droplet nuclei by evaporation at ambient air. To provide detailed, spatially-resolved information on particle deposition in the thoracic region of the lung, a top-down refinement approach was employed. Our study presents evidence for hot spots of aerosol deposition in lung generations beyond the terminal bronchiole, with a maximum in the secondary pulmonary lobules and a high preference to the lower lobes of both lungs. In vivo, initial chest CT anomalies, the ground glass opacities, resulting from partial alveolar filling and interstitial thickening in the secondary pulmonary lobules, are likewise localized in these lung generations, with the highest frequency in both lower lobes and in the early stage of disease. Hence, our results suggest a disease initiation right there upon inhalation of virion-laden respiratory aerosols, linking the aerosol transmission route to pathogenesis associated with higher disease burden and identifying aerosol transmission as a new independent risk factor for developing a pulmonary phase with a severe outcome.
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Worton, D. R., A. H. Goldstein, D. K. Farmer, K. S. Docherty, J. L. Jimenez, J. B. Gilman, W. C. Kuster et al. "Origins and composition of fine atmospheric carbonaceous aerosol in the Sierra Nevada Mountains, California". Atmospheric Chemistry and Physics Discussions 11, n.º 6 (20 de junio de 2011): 17071–125. http://dx.doi.org/10.5194/acpd-11-17071-2011.
Resumen
Abstract. In this paper we report chemically resolved measurements of organic aerosol (OA) and related tracers during the Biosphere Effects on Aerosols and Photochemistry Experiment (BEARPEX) at the Blodgett Forest Research Station, California. OA contributed the majority of the mass to the fine atmospheric particles and was predominately oxygenated (OOA). The highest concentrations of OA were during sporadic wildfire influence when aged plumes were impacting the site. In situ measurements of particle phase molecular markers were dominated by secondary compounds and could be categorized into three factors or sources: (1) aged biomass burning emissions and oxidized urban emissions, (2) oxidation products of temperature-driven local biogenic emissions and (3) local light-driven emissions and oxidation products. There were multiple biogenic components that contributed to OA at this site whose contributions varied diurnally, seasonally and in response to changing meteorological conditions, e.g., temperature and precipitation events. Concentrations of isoprene oxidation products were larger when temperatures were higher due to more substantial emissions of isoprene and enhanced photochemistry. Methyl chavicol oxidation contributed similarly to OA during both identified meteorological periods. In contrast, the abundances of monoterpene oxidation products in the particle phase were greater during cooler conditions, even though emissions of the precursors were lower. Following the first precipitation event of the fall the abundances of the monoterpene oxidation products increased dramatically, although the mechanism is not known. OA was correlated with the anthropogenic tracers 2-propyl nitrate and carbon monoxide (CO), consistent with previous observations, while being comprised of mostly non-fossil carbon (>75 %). The correlation between OA and an anthropogenic tracer does not necessarily identify the source of the carbon as being anthropogenic but instead suggests a coupling between the anthropogenic and biogenic components in the air mass that might be related to the source of the oxidant and/or the aerosol sulfate. Observations of organosulfates of isoprene and α-pinene provided evidence for the likely importance of aerosol sulfate in spite of neutralized aerosol. This is in contrast to laboratory studies where strongly acidic seed aerosols were needed in order to form these compounds. These compounds together represented only a minor fraction (< 1 %) of the total OA mass and suggest that other mechanisms, e.g., NOx enhancement of oxidant levels, are more likely to be responsible for the majority of the anthropogenic enhancement of biogenic secondary organic aerosol observed at this site.
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Worton, D. R., A. H. Goldstein, D. K. Farmer, K. S. Docherty, J. L. Jimenez, J. B. Gilman, W. C. Kuster et al. "Origins and composition of fine atmospheric carbonaceous aerosol in the Sierra Nevada Mountains, California". Atmospheric Chemistry and Physics 11, n.º 19 (12 de octubre de 2011): 10219–41. http://dx.doi.org/10.5194/acp-11-10219-2011.
Resumen
Abstract. In this paper we report chemically resolved measurements of organic aerosol (OA) and related tracers during the Biosphere Effects on Aerosols and Photochemistry Experiment (BEARPEX) at the Blodgett Forest Research Station, California from 15 August–10 October 2007. OA contributed the majority of the mass to the fine atmospheric particles and was predominately oxygenated (OOA). The highest concentrations of OA were during sporadic wildfire influence when aged plumes were impacting the site. In situ measurements of particle phase molecular markers were dominated by secondary compounds and along with gas phase compounds could be categorized into six factors or sources: (1) aged biomass burning emissions and oxidized urban emissions, (2) oxidized urban emissions (3) oxidation products of monoterpene emissions, (4) monoterpene emissions, (5) anthropogenic emissions and (6) local methyl chavicol emissions and oxidation products. There were multiple biogenic components that contributed to OA at this site whose contributions varied diurnally, seasonally and in response to changing meteorological conditions, e.g. temperature and precipitation events. Concentrations of isoprene oxidation products were larger when temperatures were higher during the first half of the campaign (15 August–12 September) due to more substantial emissions of isoprene and enhanced photochemistry. The oxidation of methyl chavicol, an oxygenated terpene emitted by ponderosa pine trees, contributed similarly to OA throughout the campaign. In contrast, the abundances of monoterpene oxidation products in the particle phase were greater during the cooler conditions in the latter half of the campaign (13 September–10 October), even though emissions of the precursors were lower, although the mechanism is not known. OA was correlated with the anthropogenic tracers 2-propyl nitrate and carbon monoxide (CO), consistent with previous observations, while being comprised of mostly non-fossil carbon (>75%). The correlation between OA and an anthropogenic tracer does not necessarily identify the source of the carbon as being anthropogenic but instead suggests a coupling between the anthropogenic and biogenic components in the air mass that might be related to the source of the oxidant and/or the aerosol sulfate. Observations of organosulfates of isoprene and α-pinene provided evidence for the likely importance of aerosol sulfate in spite of neutralized aerosol although acidic plumes might have played a role upwind of the site. This is in contrast to laboratory studies where strongly acidic seed aerosols were needed in order to form these compounds. These compounds together represented only a minor fraction (<1%) of the total OA mass, which may be the result of the neutralized aerosol at the site or because only a small number of organosulfates were quantified. The low contribution of organosulfates to total OA suggests that other mechanisms, e.g. NOx enhancement of oxidant levels, are likely responsible for the majority of the anthropogenic enhancement of biogenic secondary organic aerosol observed at this site.
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Chrit, Mounir, Karine Sartelet, Jean Sciare, Jorge Pey, Nicolas Marchand, Florian Couvidat, Karine Sellegri y Matthias Beekmann. "Modelling organic aerosol concentrations and properties during ChArMEx summer campaigns of 2012 and 2013 in the western Mediterranean region". Atmospheric Chemistry and Physics 17, n.º 20 (23 de octubre de 2017): 12509–31. http://dx.doi.org/10.5194/acp-17-12509-2017.
Resumen
Abstract. In the framework of the Chemistry-Aerosol Mediterranean Experiment, a measurement site was set up at a remote site (Ersa) on Corsica Island in the northwestern Mediterranean Sea. Measurement campaigns performed during the summers of 2012 and 2013 showed high organic aerosol concentrations, mostly from biogenic origin. This work aims to represent the organic aerosol concentrations and properties (oxidation state and hydrophilicity) using the air-quality model Polyphemus with a surrogate approach for secondary organic aerosol (SOA) formation. Biogenic precursors are isoprene, monoterpenes and sesquiterpenes. In this work, the following model oxidation products of monoterpenes are added: (i) a carboxylic acid (MBTCA) to represent multi-generation oxidation products in the low-NOx regime, (ii) organic nitrate chemistry and (iii) extremely low-volatility organic compounds (ELVOCs) formed by ozonolysis. The model shows good agreement of measurements of organic concentrations for both 2012 and 2013 summer campaigns. The modelled oxidation property and hydrophilic organic carbon properties of the organic aerosols also agree reasonably well with the measurements. The influence of the different chemical processes added to the model on the oxidation level of organics is studied. Measured and simulated water-soluble organic carbon (WSOC) concentrations show that even at a remote site next to the sea, about 64 % of the organic carbon is soluble. The concentrations of WSOC vary with the origins of the air masses and the composition of organic aerosols. The marine organic emissions only contribute to a few percent of the organic mass in PM1, with maxima above the sea.
9
Hsieh, W. C., W. D. Collins, Y. Liu, J. C. H. Chiang, C. L. Shie, K. Caldeira y L. Cao. "Climate response due to carbonaceous aerosols and aerosol-induced SST effects in NCAR community atmospheric model CAM3.5". Atmospheric Chemistry and Physics 13, n.º 15 (5 de agosto de 2013): 7489–510. http://dx.doi.org/10.5194/acp-13-7489-2013.
Resumen
Abstract. This study used the Community Atmospheric Model 3.5 (CAM3.5) to investigate the effects of carbonaceous aerosols on climate. The simulations include control runs with 3 times the mass of carbonaceous aerosols as compared to the model's default carbonaceous aerosol mass, as well as no-carbon runs in which carbonaceous aerosols were removed. The slab ocean model (SOM) and the fixed sea surface temperature (SST) were used to examine effects of ocean boundary conditions. Throughout this study, climate response induced by aerosol forcing was mainly analyzed in the following three terms: (1) aerosol radiative effects under fixed SST, (2) effects of aerosol-induced SST feedbacks, and (3) total effects including effects of aerosol forcing and SST feedbacks. The change of SST induced by aerosols has large impacts on distribution of climate response; the magnitudes in response patterns such as temperature, precipitation, zonal winds, mean meridional circulation, radiative fluxes, and cloud coverage are different between the SOM and fixed SST runs. Moreover, different spatial responses between the SOM and fixed SST runs can also be seen in some local areas. This implies the importance of SST feedbacks on simulated climate response. The aerosol dimming effects cause a cooling predicted at low layers near the surface in most carbonaceous aerosol source regions. The temperature response shows a warming (cooling) predicted in the north (south) high latitudes, suggesting that aerosol forcing can cause climate change in regions far away from its origins. Our simulation results show that direct and semidirect radiative forcing due to carbonaceous aerosols decreases rainfall in the tropics. This implies that carbonaceous aerosols have possibly strong influence on weakening of the tropical circulation. Most changes in precipitation are negatively correlated with changes of radiative fluxes at the top of model. The changes in radiative fluxes at top of model are physically consistent with the response patterns in cloud fields. On global average, low-level cloud coverage increases, and mid- and high-level cloud coverage decreases in response to changes in radiative energy induced by aerosol forcing. An approximated moisture budget equation was analyzed in order to understand physical mechanism of precipitation changes induced by carbonaceous aerosols. Our results show that changes in tropical precipitation are mainly dominated are mainly dominated by the dynamic effect (i.e., vertical moisture transport carried by the perturbed flow).
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Shcherbakov, Valery, Olivier Jourdan, Christiane Voigt, Jean-Francois Gayet, Aurélien Chauvigne, Alfons Schwarzenboeck, Andreas Minikin et al. "Porous aerosol in degassing plumes of Mt. Etna and Mt. Stromboli". Atmospheric Chemistry and Physics 16, n.º 18 (23 de septiembre de 2016): 11883–97. http://dx.doi.org/10.5194/acp-16-11883-2016.
Resumen
Abstract. Aerosols of the volcanic degassing plumes from Mt. Etna and Mt. Stromboli were probed with in situ instruments on board the Deutsches Zentrum für Luft- und Raumfahrt research aircraft Falcon during the contrail, volcano, and cirrus experiment CONCERT in September 2011. Aerosol properties were analyzed using angular-scattering intensities and particle size distributions measured simultaneously with the Polar Nephelometer and the Forward Scattering Spectrometer probes (FSSP series 100 and 300), respectively. Aerosols of degassing plumes are characterized by low values of the asymmetry parameter (between 0.6 and 0.75); the effective diameter was within the range of 1.5–2.8 µm and the maximal diameter was lower than 20 µm. A principal component analysis applied to the Polar Nephelometer data indicates that scattering features of volcanic aerosols of different crater origins are clearly distinctive from angular-scattering intensities of cirrus and contrails. Retrievals of aerosol properties revealed that the particles were "optically spherical" and the estimated values of the real part of the refractive index are within the interval from 1.35 to 1.38. The interpretation of these results leads to the conclusion that the degassing plume aerosols were porous with air voids. Our estimates suggest that aerosol particles contained about 18 to 35 % of air voids in terms of the total volume.
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Hsieh, W. C., W. D. Collins, Y. Liu, J. C. H. Chiang, C. L. Shie, K. Caldeira y L. Cao. "Climate response due to carbonaceous aerosols and aerosol-induced SST effects in NCAR community atmospheric model CAM3.5". Atmospheric Chemistry and Physics Discussions 13, n.º 3 (20 de marzo de 2013): 7349–96. http://dx.doi.org/10.5194/acpd-13-7349-2013.
Resumen
Abstract. This study used Community Atmospheric Model 3.5 (CAM3.5) to investigate the effects of carbonaceous aerosols on climate. The simulations include control runs with carbonaceous aerosols and no carbon runs in which carbonaceous aerosols were removed. The Slab Ocean Model (SOM) and the fixed Sea Surface Temperature (SST) were used to examine effects of ocean boundary conditions. Throughout this study, climate response induced by aerosol forcing was mainly analyzed in the following three terms: (1) aerosol radiative effects under fixed SST, (2) effects of aerosol-induced SST feedbacks , and (3) total effects including effects of aerosol forcing and SST feedbacks. The change of SST induced by aerosols has large impacts on distribution of climate response, the magnitudes in response patterns such as temperature, precipitation, zonal winds, mean meridional circulation, radiative fluxes and cloud coverage are different between the SOM and fixed SST runs. Moreover, different spatial responses between the SOM and fixed SST runs can also be seen in some local areas. This implies the importance of SST feedbacks on simulated climate response. The aerosol dimming effects cause a cooling predicted at low layers near the surface in most of carbonaceous aerosol source regions. The temperature response shows a warming (cooling) predicted in the north (south) high latitudes, suggesting that aerosol forcing can cause climate change in regions far away from its origins. Our simulation results show that warming of the troposphere due to black carbon decreases rainfall in the tropics. This implies that black carbon has possibly strong influence on weakening of the tropical circulation. Most of these changes in precipitation are negatively correlated with changes of radiative fluxes at the top of model. The changes in radiative fluxes at top of model are physically consistent with the response patterns in cloud fields. On global average, low-level cloud coverage increases, mid- and high-level cloud coverage decreases in response to changes in radiative energy induced by aerosol forcing. An approximated moisture budget equation was analyzed in order to understand physical mechanism of precipitation changes induced by carbonaceous aerosols. Our results show that changes in tropical precipitation are mainly dominated by dynamic effect, i.e. vertical moisture transport carried by the perturbed flow.
12
de Oliveira, Aline M., Cristina T. Souza, Nara P. M. de Oliveira, Aline K. S. Melo, Fabio J. S. Lopes, Eduardo Landulfo, Hendrik Elbern y Judith J. Hoelzemann. "Analysis of Atmospheric Aerosol Optical Properties in the Northeast Brazilian Atmosphere with Remote Sensing Data from MODIS and CALIOP/CALIPSO Satellites, AERONET Photometers and a Ground-Based Lidar". Atmosphere 10, n.º 10 (2 de octubre de 2019): 594. http://dx.doi.org/10.3390/atmos10100594.
Resumen
A 12-year analysis, from 2005 to 2016, of atmospheric aerosol optical properties focusing for the first time on Northeast Brazil (NEB) was performed based on four different remote sensing datasets: the Moderate Resolution Imaging Spectroradiometer (MODIS), the Aerosol Robotic Network (AERONET), the Cloud-Aerosol LIDAR with Orthogonal Polarization (CALIOP) and a ground-based Lidar from Natal. We evaluated and identified distinct aerosol types, considering Aerosol Optical Depth (AOD) and Angström Exponent (AE). All analyses show that over the NEB, a low aerosol scenario prevails, while there are two distinct seasons of more elevated AOD that occur every year, from August to October and January to March. According to MODIS, AOD values ranges from 0.04 to 0.52 over the region with a mean of 0.20 and occasionally isolated outliers of up to 1.21. Aerosol types were identified as sea spray, biomass burning, and dust aerosols mostly transported from tropical Africa. Three case studies on days with elevated AOD were performed. All cases identified the same aerosol types and modeled HYSPLIT backward trajectories confirmed their source-dependent origins. This analysis is motivated by the implementation of an atmospheric chemistry model with an advanced data assimilation system that will use the observational database over NEB with the model to overcome high uncertainties in the model results induced by still unvalidated emission inventories.
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Saito, Y., K. Shiraishi, A. Nishimura, T. Kirinaka, Y. Sakurai y T. Tomida. "Fluorescence Database of Aerosol-Candidate-Substances for Fluorescence Lidar Application". EPJ Web of Conferences 237 (2020): 07016. http://dx.doi.org/10.1051/epjconf/202023707016.
Resumen
A database containing spectrum and cross-section of the fluorescence of substances has been made. In test of forest environment monitoring by our Laser-Induced Fluorescence Spectrum (LIFS) lidar, the database showed that the origin substance of the aerosol observed by the lidar was cedar pollen, and the concentration was calculated using the cross-section. In the urban atmosphere monitoring, three substances stored in the database were proposed to be the origins of the aerosol. Based on these experiments, we discuss the usefulness of the fluorescence database in lidar observations.
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Takahama, S., R. E. Schwartz, L. M. Russell, A. M. Macdonald, S. Sharma y W. R. Leaitch. "Organic functional groups in aerosol particles from burning and non-burning forest emissions at a high-elevation mountain site". Atmospheric Chemistry and Physics 11, n.º 13 (6 de julio de 2011): 6367–86. http://dx.doi.org/10.5194/acp-11-6367-2011.
Resumen
Abstract. Ambient particles collected on teflon filters at the Peak of Whistler Mountain, British Columbia (2182 m a.s.l.) during spring and summer 2009 were measured by Fourier transform infrared (FTIR) spectroscopy for organic functional groups (OFG). The project mean and standard deviation of organic aerosol mass concentrations (OM) for all samples was 3.2±3.3 (μg m−3). Measurements of aerosol mass fragments, size, and number concentrations were used to separate fossil-fuel combustion and burning and non-burning forest sources of the measured organic aerosol. The OM was composed of the same anthropogenic and non-burning forest components observed at Whistler mid-valley in the spring of 2008; during the 2009 campaign, biomass burning aerosol was additionally observed from fire episodes occurring between June and September. On average, organic hydroxyl, alkane, carboxylic acid, ketone, and primary amine groups represented 31 %±11 %, 34 %±9 %, 23 %±6 %, 6 %±7 %, and 6 %±3 % of OM, respectively. Ketones in aerosols were associated with burning and non-burning forest origins, and represented up to 27 % of the OM. The organic aerosol fraction resided almost entirely in the submicron fraction without significant diurnal variations. OM/OC mass ratios ranged mostly between 2.0 and 2.2 and O/C atomic ratios between 0.57 and 0.76, indicating that the organic aerosol reaching the site was highly aged and possibly formed through secondary formation processes.
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Cazorla, A., R. Bahadur, K. J. Suski, J. F. Cahill, D. Chand, B. Schmid, V. Ramanathan y K. Prather. "Relating aerosol absorption due to soot, organic carbon, and dust to emission sources determined from in-situ chemical measurements". Atmospheric Chemistry and Physics Discussions 13, n.º 2 (6 de febrero de 2013): 3451–83. http://dx.doi.org/10.5194/acpd-13-3451-2013.
Resumen
Abstract. Estimating the aerosol contribution to the global or regional radiative forcing can take advantage of the relationship between the spectral aerosol optical properties and the size and chemical composition of aerosol. Long term global optical measurements from observational networks or satellites can be used in such studies. Using in-situ chemical mixing state measurements can help us to constrain the limitations of such estimates. In this study, the Absorption Ångström Exponent (AAE) and the Scattering Ångström Exponent (SAE) derived from 10 operational AERONET sites in California are combined for deducing chemical speciation based on wavelength dependence of the optical properties. In addition, in-situ optical properties and single particle chemical composition measured during three aircraft field campaigns in California between 2010 and 2011 are combined in order to validate the methodology used for the estimates of aerosol composition using spectral optical properties. Results from this study indicate a dominance of mixed types in the classification leading to an underestimation of the primary sources, however secondary sources are better classified. The distinction between carbonaceous aerosols from fossil fuel and biomass burning origins is not clear, since their optical properties are similar. On the other hand, knowledge of the aerosol sources in California from chemical studies help to identify other misclassification such as the dust contribution.
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Cazorla, A., R. Bahadur, K. J. Suski, J. F. Cahill, D. Chand, B. Schmid, V. Ramanathan y K. A. Prather. "Relating aerosol absorption due to soot, organic carbon, and dust to emission sources determined from in-situ chemical measurements". Atmospheric Chemistry and Physics 13, n.º 18 (17 de septiembre de 2013): 9337–50. http://dx.doi.org/10.5194/acp-13-9337-2013.
Resumen
Abstract. Estimating the aerosol contribution to the global or regional radiative forcing can take advantage of the relationship between the spectral aerosol optical properties and the size and chemical composition of aerosol. Long term global optical measurements from observational networks or satellites can be used in such studies. Using in-situ chemical mixing state measurements can help us to constrain the limitations of such estimates. In this study, the Absorption Ångström Exponent (AAE) and the Scattering Ångström Exponent (SAE) derived from 10 operational AERONET sites in California are combined for deducing chemical speciation based on wavelength dependence of the optical properties. In addition, in-situ optical properties and single particle chemical composition measured during three aircraft field campaigns in California between 2010 and 2011 are combined in order to validate the methodology used for the estimates of aerosol chemistry using spectral optical properties. Results from this study indicate a dominance of mixed types in the classification leading to an underestimation of the primary sources, however secondary sources are better classified. The distinction between carbonaceous aerosols from fossil fuel and biomass burning origins is not clear, since their optical properties are similar. On the other hand, knowledge of the aerosol sources in California from chemical studies help to identify other misclassification such as the dust contribution.
17
Ulke, Ana G. "Influence of Regional Transport Mechanisms on the Fingerprint of Biomass-Burning Aerosols in Buenos Aires". Advances in Meteorology 2019 (29 de diciembre de 2019): 1–13. http://dx.doi.org/10.1155/2019/6792161.
Resumen
The study focuses on the transport of aerosol particles resulting from biomass burning in central South America towards the megacity of Buenos Aires by the South American Low-Level Jet. In particular, the cases are studied in which the exit area of the Jet reaches the La Plata Basin with no precipitation associated, herein called Chaco Jet 1 (CJ1), which could remove aerosols from the atmosphere on their way towards the city. CJ1 events registered within the five-year period of 2001–2005 are examined along with changes in the optical properties of aerosols over the city from measurements from the Aerosol Robotic Network (AERONET) site. Three-dimensional backward trajectories of CJ1 were obtained to verify the connection between the receptor site and the biomass-burning source region. A cluster analysis of the trajectories allows further characterizing the features and impacts of regionally transported aerosols. A subsample of days on which impacts of the contribution of biomass burning could have occurred, showed a statistically significant increase in aerosol optical depth and Ångström exponent, reflected by an increase in the peak of the derived volume size distribution in the fine fraction size range, which also shifts slightly towards bigger radii. The days with AOD greater than 0.15 show overall behaviour like other urban sites with pollution of different origins. The evaluation of the selected data reveals that higher values of AOD and changes in the Ångström exponent are linked to the dispersion of biomass-burning aerosols. Air mass trajectories coinciding with the CJ1 core present the strongest impact on aerosol characteristics, which can be seen in spectral measurements.
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Gallo, Francesca, Janek Uin, Kevin J. Sanchez, Richard H. Moore, Jian Wang, Robert Wood, Fan Mei et al. "Long-range transported continental aerosol in the eastern North Atlantic: three multiday event regimes influence cloud condensation nuclei". Atmospheric Chemistry and Physics 23, n.º 7 (6 de abril de 2023): 4221–46. http://dx.doi.org/10.5194/acp-23-4221-2023.
Resumen
Abstract. The eastern North Atlantic (ENA) is a region dominated by pristine marine environment and subtropical marine boundary layer clouds. Under unperturbed atmospheric conditions, the regional aerosol regime in the ENA varies seasonally due to different seasonal surface-ocean biogenic emissions, removal processes, and meteorological regimes. However, during periods when the marine boundary layer aerosol in the ENA is impacted by particles transported from continental sources, aerosol properties within the marine boundary layer change significantly, affecting the concentration of cloud condensation nuclei (CCN). Here, we investigate the impact of long-range transported continental aerosol on the regional aerosol regime in the ENA using data collected at the U.S. Department of Energy's (DOE) Atmospheric Radiation Measurement (ARM) user facility on Graciosa Island in 2017 during the Aerosol and Cloud Experiments in the Eastern North Atlantic (ACE-ENA) campaign. We develop an algorithm that integrates number concentrations of particles with optical particle dry diameter (Dp) between 100 and 1000 nm, single scattering albedo, and black carbon concentration to identify multiday events (with duration >24 consecutive hours) of long-range continental aerosol transport in the ENA. In 2017, we detected nine multiday events of long-range transported particles that correspond to ∼ 7.5 % of the year. For each event, we perform HYSPLIT 10 d backward trajectories analysis, and we evaluate CALIPSO aerosol products to assess, respectively, the origins and compositions of aerosol particles arriving at the ENA site. Subsequently, we group the events into three categories, (1) mixture of dust and marine aerosols, (2) mixture of marine and polluted continental aerosols from industrialized areas, and (3) biomass burning aerosol from North America and Canada, and we evaluate their influence on aerosol population and cloud condensation nuclei in terms of potential activation fraction and concentrations at supersaturation of 0.1 % and 0.2 %. The arrival of plumes dominated by the mixture of dust and marine aerosol in the ENA in the winter caused significant increases in baseline Ntot. Simultaneously, the baseline particle size modes and CCN potential activation fraction remained almost unvaried, while cloud condensation nuclei concentrations increased proportionally to Ntot. Events dominated by a mixture of marine and polluted continental aerosols in spring, fall, and winter led to a statistically significant increase in baseline Ntot, a shift towards larger particular sizes, a higher CCN potential activation fractions, and cloud condensation nuclei concentrations of >170 % and up to 240 % higher than during baseline regime. Finally, the transported aerosol plumes characterized by elevated concentration of biomass burning aerosol from continental wildfires detected in the summertime did not statistically contribute to increase baseline aerosol particle concentrations in the ENA. However, particle diameters were larger than under baseline conditions, and CCN potential activation fractions were >75 % higher. Consequentially, cloud concentration nuclei concentrations increased by ∼ 115 % during the period affected by the biomass burning events. Our results suggest that, through the year, multiday events of long-range continental aerosol transport periodically affect the ENA and represent a significant source of CCN in the marine boundary layer. Based on our analysis, in 2017, the multiday aerosol plume transport dominated by a mixture of dust and marine aerosol, a mixture of marine and polluted continental aerosols, and biomass burning aerosols caused increases in the NCCN baseline regime of, respectively, 6.6 %, 8 %, and 7.4 % at SS 0.1 % (and, respectively, 6.5 %, 8.2 %, and 7.3 % at SS 0.2 %) in the ENA.
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Sheoran, Rahul, Umesh Chandra Dumka, Dimitris G. Kaskaoutis, Georgios Grivas, Kirpa Ram, Jai Prakash, Rakesh K. Hooda, Rakesh K. Tiwari y Nikos Mihalopoulos. "Chemical Composition and Source Apportionment of Total Suspended Particulate in the Central Himalayan Region". Atmosphere 12, n.º 9 (19 de septiembre de 2021): 1228. http://dx.doi.org/10.3390/atmos12091228.
Resumen
The present study analyzes data from total suspended particulate (TSP) samples collected during 3 years (2005–2008) at Nainital, central Himalayas, India and analyzed for carbonaceous aerosols (organic carbon (OC) and elemental carbon (EC)) and inorganic species, focusing on the assessment of primary and secondary organic carbon contributions (POC, SOC, respectively) and on source apportionment by positive matrix factorization (PMF). An average TSP concentration of 69.6 ± 51.8 µg m−3 was found, exhibiting a pre-monsoon (March–May) maximum (92.9 ± 48.5 µg m−3) due to dust transport and forest fires and a monsoon (June–August) minimum due to atmospheric washout, while carbonaceous aerosols and inorganic species expressed a similar seasonality. The mean OC/EC ratio (8.0 ± 3.3) and the good correlations between OC, EC, and nss-K+ suggested that biomass burning (BB) was one of the major contributing factors to aerosols in Nainital. Using the EC tracer method, along with several approaches for the determination of the (OC/EC)pri ratio, the estimated SOC component accounted for ~25% (19.3–29.7%). Furthermore, TSP source apportionment via PMF allowed for a better understanding of the aerosol sources in the Central Himalayan region. The key aerosol sources over Nainital were BB (27%), secondary sulfate (20%), secondary nitrate (9%), mineral dust (34%), and long-range transported mixed marine aerosol (10%). The potential source contribution function (PSCF) and concentration weighted trajectory (CWT) analyses were also used to identify the probable regional source areas of resolved aerosol sources. The main source regions for aerosols in Nainital were the plains in northwest India and Pakistan, polluted cities like Delhi, the Thar Desert, and the Arabian Sea area. The outcomes of the present study are expected to elucidate the atmospheric chemistry, emission source origins, and transport pathways of aerosols over the central Himalayan region.
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Gobbi, G. P., F. Angelini, P. Bonasoni, G. P. Verza, A. Marinoni y F. Barnaba. "Sunphotometry of the 2006–2007 aerosol optical/radiative properties at the Himalayan Nepal Climate Observatory-Pyramid (5079 m a.s.l.)". Atmospheric Chemistry and Physics 10, n.º 22 (29 de noviembre de 2010): 11209–21. http://dx.doi.org/10.5194/acp-10-11209-2010.
Resumen
Abstract. In spite of being located at the heart of the highest mountain range in the world, the Himalayan Nepal Climate Observatory (5079 m a.s.l.) at the Ev-K2-CNR Pyramid is shown to be affected by the advection of pollution aerosols from the populated regions of southern Nepal and the Indo-Gangetic plains. Such an impact is observed along most of the period April 2006–March 2007 addressed here, with a minimum in the monsoon season. Backtrajectory-analysis indicates long-range transport episodes occurring in this year to originate mainly in the west Asian deserts. At this high altitude site, the measured aerosol optical depth is observed to be about one order of magnitude lower than the one measured at Ghandi College (60 m a.s.l.), in the Indo-Gangetic basin. As for Ghandi College, and in agreement with the in situ ground observations at the Pyramid, the fine mode aerosol optical depth maximizes during winter and minimizes in the monsoon season. Conversely, total optical depth maximizes during the monsoon due to the occurrence of elevated, coarse particle layers. Possible origins of these particles are wind erosion from the surrounding peaks and hydrated/cloud-processed aerosols. Assessment of the aerosol radiative forcing is then expected to be hampered by the presence of these high altitude particle layers, which impede an effective, continuous measurement of anthropogenic aerosol radiative properties from sky radiance inversions and/or ground measurements alone. Even though the retrieved absorption coefficients of pollution aerosols were rather large (single scattering albedo of the order of 0.6–0.9 were observed in the month of April 2006), the corresponding low optical depths (~0.03 at 500 nm) are expected to limit the relevant radiative forcing. Still, the high specific forcing of this aerosol and its capability of altering snow surface albedo provide good reasons for continuous monitoring.
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Law, Katharine S., Andreas Stohl, Patricia K. Quinn, Charles A. Brock, John F. Burkhart, Jean-Daniel Paris, Gerard Ancellet et al. "Arctic Air Pollution: New Insights from POLARCAT-IPY". Bulletin of the American Meteorological Society 95, n.º 12 (1 de diciembre de 2014): 1873–95. http://dx.doi.org/10.1175/bams-d-13-00017.1.
Resumen
Given the rapid nature of climate change occurring in the Arctic and the difficulty climate models have in quantitatively reproducing observed changes such as sea ice loss, it is important to improve understanding of the processes leading to climate change in this region, including the role of short-lived climate pollutants such as aerosols and ozone. It has long been known that pollution produced from emissions at midlatitudes can be transported to the Arctic, resulting in a winter/spring aerosol maximum known as Arctic haze. However, many uncertainties remain about the composition and origin of Arctic pollution throughout the troposphere; for example, many climate–chemistry models fail to reproduce the strong seasonality of aerosol abundance observed at Arctic surface sites, the origin and deposition mechanisms of black carbon (soot) particles that darken the snow and ice surface in the Arctic is poorly understood, and chemical processes controlling the abundance of tropospheric ozone are not well quantified. The International Polar Year (IPY) Polar Study using Aircraft, Remote Sensing, Surface Measurements and Models, Climate, Chemistry, Aerosols and Transport (POLARCAT) core project had the goal to improve understanding about the origins of pollutants transported to the Arctic; to detail the chemical composition, optical properties, and climate forcing potential of Arctic aerosols; to evaluate the processes governing tropospheric ozone; and to quantify the role of boreal forest fires. This article provides a review of the many results now available based on analysis of data collected during the POLARCAT aircraft-, ship-, and ground-based field campaigns in spring and summer 2008. Major findings are highlighted and areas requiring further investigation are discussed.
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Hara, Keiichiro, Chiharu Nishita-Hara, Kazuo Osada, Masanori Yabuki y Takashi Yamanouchi. "Characterization of aerosol number size distributions and their effect on cloud properties at Syowa Station, Antarctica". Atmospheric Chemistry and Physics 21, n.º 15 (13 de agosto de 2021): 12155–72. http://dx.doi.org/10.5194/acp-21-12155-2021.
Resumen
Abstract. We took aerosol measurements at Syowa Station, Antarctica, to characterize the aerosol number–size distribution and other aerosol physicochemical properties in 2004–2006. Four modal structures (i.e., mono-, bi-, tri-, and quad-modal) were identified in aerosol size distributions during measurements. Particularly, tri-modal and quad-modal structures were associated closely with new particle formation (NPF). To elucidate where NPF proceeds in the Antarctic, we compared the aerosol size distributions and modal structures to air mass origins computed using backward trajectory analysis. Results of this comparison imply that aerosol size distributions involved with fresh NPF (quad-modal distributions) were observed in coastal and continental free troposphere (FT; 12 % of days) areas and marine and coastal boundary layers (1 %) during September–October and March and in coastal and continental FT (3 %) areas and marine and coastal boundary layers (8 %) during December–February. Photochemical gaseous products, coupled with ultraviolet (UV) radiation, play an important role in NPF, even in the Antarctic troposphere. With the existence of the ozone hole in the Antarctic stratosphere, more UV radiation can enhance atmospheric chemistry, even near the surface in the Antarctic. However, linkage among tropospheric aerosols in the Antarctic, ozone hole, and UV enhancement is unknown. Results demonstrated that NPF started in the Antarctic FT already at the end of August–early September by UV enhancement resulting from the ozone hole. Then, aerosol particles supplied from NPF during periods when the ozone hole appeared to grow gradually by vapor condensation, suggesting modification of aerosol properties such as number concentrations and size distributions in the Antarctic troposphere during summer. Here, we assess the hypothesis that UV enhancement in the upper troposphere by the Antarctic ozone hole modifies the aerosol population, aerosol size distribution, cloud condensation nuclei capabilities, and cloud properties in Antarctic regions during summer.
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Chazette, Patrick, Julien Totems y Xiaoxia Shang. "Transport of aerosols over the French Riviera – link between ground-based lidar and spaceborne observations". Atmospheric Chemistry and Physics 19, n.º 6 (26 de marzo de 2019): 3885–904. http://dx.doi.org/10.5194/acp-19-3885-2019.
Resumen
Abstract. For the first time, a 355 nm backscatter N2-Raman lidar has been deployed on the western part of the French Riviera to investigate the vertical aerosol structure in the troposphere. This lidar system, based at the AERONET site of Toulon–La Garde, performed continuous measurements from 24 June to 17 July 2014, within the framework of the multidisciplinary program Mediterranean Integrated Studies at the Regional and Local Scales (MISTRALS). By coupling these observations with those of the spaceborne instruments Cloud-Aerosol LIdar with Orthogonal Polarization (CALIOP), Spinning Enhanced Visible and InfraRed Imager (SEVIRI), and Moderate Resolution Imaging Spectroradiometers (MODIS), the spatial extents of the aerosol structures are investigated. The origins of the aerosol plumes are determined using back trajectories computed by the Hybrid Single Particle Lagrangian Integrated Trajectory (HYSPLIT). This synergy allowed us to highlight plumes of particulate pollutants moving in the low and medium free troposphere (up to ∼5 km above the mean sea level) towards the French Riviera. This pollution originates from the Spanish coast, more particularly from Costa Blanca (including Murcia) and Costa Brava–Costa Daurada (including Barcelona). It is mainly due to traffic, but also to petrochemical activities in these two regions. Desert aerosol plumes were also sampled by the lidar. The sources of desert aerosols have been identified as the Grand Erg Occidental and Grand Erg Oriental. During desert dust events, we highlight significant differences in the optical characteristics in terms of the backscatter-to-extinction ratio (BER, inverse of the lidar ratio) between the planetary boundary layer, with 0.024 sr−1 (∼42 sr), and the free troposphere, with 0.031 sr−1 (∼32 sr). These differences are greatly reduced in the case of pollution aerosol plume transport in the free troposphere (i.e., 0.021 and 0.025 sr−1). Transported pollution aerosols appear to have similar BER to what is emitted locally. Moreover, using the correlation matrix between lidar aerosol extinction profiles as a function of altitude, we find that during transport events in the low free troposphere, aerosols may be transferred into the planetary boundary layer. We also note that the relative humidity, which is generally higher in the planetary boundary layer (>80 %), is found to have no significant effect on the BER.
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Moschos, Vaios, Julia Schmale, Wenche Aas, Silvia Becagli, Giulia Calzolai, Konstantinos Eleftheriadis, Claire E. Moffett et al. "Elucidating the present-day chemical composition, seasonality and source regions of climate-relevant aerosols across the Arctic land surface". Environmental Research Letters 17, n.º 3 (28 de febrero de 2022): 034032. http://dx.doi.org/10.1088/1748-9326/ac444b.
Resumen
Abstract The Arctic is warming two to three times faster than the global average, and the role of aerosols is not well constrained. Aerosol number concentrations can be very low in remote environments, rendering local cloud radiative properties highly sensitive to available aerosol. The composition and sources of the climate-relevant aerosols, affecting Arctic cloud formation and altering their microphysics, remain largely elusive due to a lack of harmonized concurrent multi-component, multi-site, and multi-season observations. Here, we present a dataset on the overall chemical composition and seasonal variability of the Arctic total particulate matter (with a size cut at 10 μm, PM10, or without any size cut) at eight observatories representing all Arctic sectors. Our holistic observational approach includes the Russian Arctic, a significant emission source area with less dedicated aerosol monitoring, and extends beyond the more traditionally studied summer period and black carbon/sulfate or fine-mode pollutants. The major airborne Arctic PM components in terms of dry mass are sea salt, secondary (non-sea-salt, nss) sulfate, and organic aerosol (OA), with minor contributions from elemental carbon (EC) and ammonium. We observe substantial spatiotemporal variability in component ratios, such as EC/OA, ammonium/nss-sulfate and OA/nss-sulfate, and fractional contributions to PM. When combined with component-specific back-trajectory analysis to identify marine or terrestrial origins, as well as the companion study by Moschos et al 2022 Nat. Geosci. focusing on OA, the composition analysis provides policy-guiding observational insights into sector-based differences in natural and anthropogenic Arctic aerosol sources. In this regard, we first reveal major source regions of inner-Arctic sea salt, biogenic sulfate, and natural organics, and highlight an underappreciated wintertime source of primary carbonaceous aerosols (EC and OA) in West Siberia, potentially associated with the oil and gas sector. The presented dataset can assist in reducing uncertainties in modelling pan-Arctic aerosol-climate interactions, as the major contributors to yearly aerosol mass can be constrained. These models can then be used to predict the future evolution of individual inner-Arctic atmospheric PM components in light of current and emerging pollution mitigation measures and improved region-specific emission inventories.
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Samaranayake, Lakshman. "COVID-19 and Dentistry: Aerosol and Droplet Transmission of SARS-CoV-2, and Its Infectivity in Clinical Settings". Dental Update 47, n.º 7 (2 de julio de 2020): 600–602. http://dx.doi.org/10.12968/denu.2020.47.7.600.
Resumen
In the last inaugural issue of the Commentary we discussed the origins of the SARS-CoV-2, the probable reasons for its emergence, and how the virus spreads due to the rapid, inter-continental, mass transportation, as well as the human behaviour leading to deforestation and massive urbanization and environmental changes. Here, we outline the issues surrounding infectivity of the SARS-CoV-2, plus its spread through aerosols, droplets and aerosol generating procedures (AGPs) in the dental clinic milieu, as well as its viability in the ambient environment.
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Petit, Jean-Eudes, Cyril Pallarès, Olivier Favez, Laurent Y. Alleman, Nicolas Bonnaire y Emmanuel Rivière. "Sources and Geographical Origins of PM10 in Metz (France) Using Oxalate as a Marker of Secondary Organic Aerosols by Positive Matrix Factorization Analysis". Atmosphere 10, n.º 7 (3 de julio de 2019): 370. http://dx.doi.org/10.3390/atmos10070370.
Resumen
An original source apportionment study was conducted on atmospheric particles (PM10) collected in Metz, one of the largest cities of Eastern France. A Positive matrix factorization (PMF) analysis was applied to a sampling filter-based chemical dataset obtained for the April 2015 to January 2017 period. Nine factors were clearly identified, showing mainly contributions from anthropogenic sources of primary PM (19.2% and 16.1% for traffic and biomass burning, respectively) as well as secondary aerosols (12.3%, 14.5%, 21.8% for sulfate-, nitrate-, and oxalate-rich factors, respectively). Wood-burning aerosols exhibited strong temporal variations and contributed up to 30% of the PM mass fraction during winter, while primary traffic concentrations remained relatively constant throughout the year. These two sources are also the main contributors during observed PM10 pollution episodes. Furthermore, the dominance of the oxalate-rich factor among other secondary aerosol factors underlines the role of atmospheric processing to secondary organic aerosol loadings which are still poorly characterized in this region. Finally, Concentration-Weighted Trajectory (CWT) analysis were performed to investigate the geographical origins of the apportioned sources, notably illustrating a significant transport of both nitrate-rich and sulfate-rich factors from Northeastern Europe but also from the Balkan region.
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Zabukovec, Antonin, Gerard Ancellet, Iwan E. Penner, Mikhail Arshinov, Valery Kozlov, Jacques Pelon, Jean-Daniel Paris et al. "Characterization of Aerosol Sources and Optical Properties in Siberia Using Airborne and Spaceborne Observations". Atmosphere 12, n.º 2 (11 de febrero de 2021): 244. http://dx.doi.org/10.3390/atmos12020244.
Resumen
Airborne backscatter lidar at 532 nm and in-situ measurements of black carbon (BC), carbon monoxide excess above background (ΔCO), and aerosol size distribution were carried out over Siberia in July 2013 and June 2017 in order to sample several kinds of aerosol sources. Aerosol types are derived using the Lagrangian FLEXible PARTicle dispersion model (FLEXPART) simulations and satellite observations. Six aerosol types could be identified in this work: (i) dusty aerosol mixture, (ii) Ob valley gas flaring emission, (iii) fresh forest fire, (iv) aged forest fire, (v) urban emissions over the Tomsk/Novosibirsk region (vi) long range transport of Northern China urban emission. The altitude range of aerosol layers is discussed for each aerosol type, showing transport above the boundary layer for long range transport of Northern China emissions or fresh forest fire. Comparisons of aerosol optical properties, BC and ΔCO are made between aged and fresh plumes for both the urban and forest fire emissions. An increase of aerosol optical depth at 532 nm (AOD532), aerosol particle size and ΔCO is found for aged forest fire plumes. Similar results are obtained when comparing the aged urban plume from Northern China with fresh urban emissions from Siberian cities. A flight above gas flaring emissions corresponds to the largest AOD532 and provides a possible range of 50–60 sr for the lidar ratio of these aerosol plumes often encountered in Siberia. Black carbon concentrations are relatively higher for the flaring plume (0.4–0.5 μμg.m−3) than for the urban plume (0.2 μμg.m−3). The largest BC concentrations are found for the fresh forest fire plume. The aerosol type identification and AOD532 provided by CALIOP Version 4.2 data products in air masses with similar origin generally agree with the results obtained from our detailed analysis of the aerosol plume origins.
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Hansen, J., M. Sato, P. Kharecha y K. von Schuckmann. "Earth's energy imbalance and implications". Atmospheric Chemistry and Physics 11, n.º 24 (22 de diciembre de 2011): 13421–49. http://dx.doi.org/10.5194/acp-11-13421-2011.
Resumen
Abstract. Improving observations of ocean heat content show that Earth is absorbing more energy from the Sun than it is radiating to space as heat, even during the recent solar minimum. The inferred planetary energy imbalance, 0.58 ± 0.15 W m−2 during the 6-yr period 2005–2010, confirms the dominant role of the human-made greenhouse effect in driving global climate change. Observed surface temperature change and ocean heat gain together constrain the net climate forcing and ocean mixing rates. We conclude that most climate models mix heat too efficiently into the deep ocean and as a result underestimate the negative forcing by human-made aerosols. Aerosol climate forcing today is inferred to be −1.6 ± 0.3 W m−2, implying substantial aerosol indirect climate forcing via cloud changes. Continued failure to quantify the specific origins of this large forcing is untenable, as knowledge of changing aerosol effects is needed to understand future climate change. We conclude that recent slowdown of ocean heat uptake was caused by a delayed rebound effect from Mount Pinatubo aerosols and a deep prolonged solar minimum. Observed sea level rise during the Argo float era is readily accounted for by ice melt and ocean thermal expansion, but the ascendency of ice melt leads us to anticipate acceleration of the rate of sea level rise this decade.
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Velazquez-Garcia, Alejandra, Joel F. de Brito, Suzanne Crumeyrolle, Isabelle Chiapello y Véronique Riffault. "Assessment of light-absorbing carbonaceous aerosol origins and properties at the ATOLL site in northern France". Aerosol Research 2, n.º 1 (28 de mayo de 2024): 107–22. http://dx.doi.org/10.5194/ar-2-107-2024.
Resumen
Abstract. Understanding the lifecycle of light-absorbing carbonaceous aerosols, from emission to deposition, is critical for assessing their climate impact. This study integrated multi-year aerosol observations from the ATOLL (ATmospheric Observations in liLLe, northern France) platform, with air mass back trajectories and emission inventory as a newly developed “INTERPLAY” (IN-siTu obsERvations, hysPLit, And emission inventorY) approach. Applied to black carbon (BC), the method apportioned source contributions (shipping, vehicular, residential heating, industrial) and studied aerosol aging effects, notably on the brown carbon (BrC) component. Results estimate that, throughout the year, vehicular traffic dominated BC (31 %), followed by shipping (25 %, of which one-third was from canals/rivers) and residential heating (21 %). Comparing INTERPLAY results with the aethalometer model highlights that the “residential sector” BC can be entirely apportioned to BC from wood burning (BCwb), notably in winter, while vehicular traffic corresponds to only about 41 % of BC fossil fuel (BCff) at the ATOLL site, the rest being apportioned to shipping (33 %) and industrial (23 %) emissions. Thus, vehicular traffic and BCff should not be used interchangeably, particularly in regions near intense maritime traffic. Concerning BrC, our analysis confirms a dominant role of residential heating. Focusing on winter, results suggest a considerable decrease in the BrC component only 24 h after emission, with fresh residential emissions being responsible for 72 % of BrC absorption at ATOLL. The results from this study allow for an improved understanding of sources and atmospheric dynamics of light-absorbing carbonaceous aerosols in northern France, being crucial for both source abatement strategies as well as a better assessment of their climate impact.
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Toledano, C., V. E. Cachorro, A. M. de Frutos, B. Torres, A. Berjón, M. Sorribas y R. S. Stone. "Airmass Classification and Analysis of Aerosol Types at El Arenosillo (Spain)". Journal of Applied Meteorology and Climatology 48, n.º 5 (1 de mayo de 2009): 962–81. http://dx.doi.org/10.1175/2008jamc2006.1.
Resumen
Abstract The Aerosol Robotic Network (AERONET) site “El Arenosillo,” equipped with a Cimel sun photometer, has been in operation since 2000. The data collected there are analyzed to establish an aerosol synoptic climatological description that is representative of the region. Different air masses and aerosol types are present over the site depending on the synoptic conditions. The frequent intrusion of dust from the Sahara Desert at El Arenosillo suggested the use of back trajectories to determine the airmass origins of other types of aerosol observed there. The focus of this study is to classify the air masses arriving at El Arenosillo by means of back-trajectory analyses and to characterize the aerosol within each type by means of the aerosol optical depth (AOD) and its spectral signature, given as the Ångström exponent (AE). The goal is to determine how aerosols observed over the station (receptor site) differ depending on source region and transport pathways. Two classification methods are used, one based on sectors and a second based on cluster analysis. The period analyzed is from 2000 to 2004. Both methods show that maritime air masses are predominant, occurring 70% of the time and having relatively low AOD (≈0.1 at 440 nm) and a wide range of AE (from about 0 to 2.0). Air masses with continental characteristics are moderately turbid and have values of AE that average ≈1.4. Air masses arriving from the south and southwest show the distinct features of the desert dust, having moderate to high values of AOD (0.30–0.35 at 440 nm) and low values of AE.
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Dupuy, R., P. Laj y K. Sellegri. "Cn to ccn relationships and cloud microphysical properties in different air masses at a free tropospheric site". Atmospheric Chemistry and Physics Discussions 6, n.º 1 (1 de febrero de 2006): 879–98. http://dx.doi.org/10.5194/acpd-6-879-2006.
Resumen
Abstract. The fraction of aerosol particles activated to droplets (CCN) is often derived from semi-empirical relationships that commonly tend to overestimate droplet number concentration leading to major uncertainties in global climate models. One of the difficulties in relating aerosol concentration to cloud microphysics and cloud albedo lies in the necessity of working at a constant liquid water path (LWP), which is very difficult to control. In this study we observed the relationships between aerosol number concentration (NCN), cloud droplet concentration (Nd) and effective radius (Reff), at the Puy de Dôme (France). A total of 20 cloud events were sampled representing a period of more than 250 h of cloud sampling. Samples are classified first according to air mass origins (Modified Marine, Continental and Polluted) and then according to their liquid water content (Thin, Medium and Thick clouds). The CCN fraction of aerosols appears to vary significantly according to the air mass origin. It is maximum for Continental air masses and minimum for Polluted air masses. Surprisingly, the CCN fraction of Modified Marine air masses fraction is lower than the continental air mass and from expected from previous studies. The limited number of activated particles in Modified Marine air masses is most likely the result of the presence of hydrophobic organic compounds. The limited activation effect leads to a 0.5 to 1 μm increase in Reff with respect to an ideal Marine case. This is significant and implies that the dReff/dNCN of low-continental clouds is higher than expected.
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Fomba, K. W., D. van Pinxteren, K. Müller, Y. Iinuma, T. Lee, J. Collet Jr. y H. Herrmann. "Trace metal characterization of aerosol particles and cloud water during HCCT 2010". Atmospheric Chemistry and Physics Discussions 15, n.º 7 (14 de abril de 2015): 10899–938. http://dx.doi.org/10.5194/acpd-15-10899-2015.
Resumen
Abstract. Trace metal characterization of bulk and size resolved aerosol and cloud water samples were performed during the Hill Cap Cloud Thuringia (HCCT) campaign. Cloud water was collected at the top of Mt. Schmücke while aerosol samples were collected at two stations upwind and downwind of Mt. Schmücke. Fourteen trace metals including Ti, V, Fe, Mn, Co, Zn, Ni, Cu, As, Sr, Rb, Pb, Cr, and Se were investigated during four full cloud events (FCE) that fulfilled the conditions of a continuous air mass flow through the three stations. Aerosol particle trace metal concentrations were found to be lower than those observed in the same region during previous field experiments but were within a similar range to those observed in other rural regions in Europe. Fe and Zn were the most abundant elements with concentration ranges of 0.2–111.6 and 1.1–32.1 ng m−3, respectively. Fe, Mn and Ti were mainly found in coarse mode aerosols while Zn, Pb and As were mostly found in the fine mode. Correlation and enrichment factor analysis of trace metals revealed that trace metals such as Ti and Rb were mostly of crustal origin while trace metals such as Zn, Pb, As, Cr, Ni, V, and Cu were of anthropogenic origin. Trace metals such as Fe, Mn, were of mixed origins including crustal and combustion sources. Trace metal cloud water concentration decreased from Ti, Mn, Cr, to Co with average concentrations of 9.18, 5.59, 5.54, and 0.46 μg L−1, respectively. A non-uniform distribution of soluble Fe, Cu and Mn was observed across the cloud drop sizes. Soluble Fe and Cu were found mainly in cloud droplets with diameters between 16 and 22 μm while Mn was found mostly in larger drops greater than 22 μm. Fe (III) was the main form of soluble Fe especially in the small and larger drops with concentrations ranging from 2.2 to 37.1 μg L−1. In contrast to other studies, Fe (II) was observed mainly in the evening hours, implying its presence was not directly related to photochemical processes. Aerosol cloud interaction did not lead to a mark increase in soluble trace metal concentrations, but led to differences in the chemical composition of the aerosol due to preferential loss of aerosol particles through physical processes including cloud drop deposition to vegetative surfaces.
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Fomba, K. W., D. van Pinxteren, K. Müller, Y. Iinuma, T. Lee, J. L. Collett y H. Herrmann. "Trace metal characterization of aerosol particles and cloud water during HCCT 2010". Atmospheric Chemistry and Physics 15, n.º 15 (10 de agosto de 2015): 8751–65. http://dx.doi.org/10.5194/acp-15-8751-2015.
Resumen
Abstract. Trace metal characterization of bulk and size-resolved aerosol and cloud water samples were performed during the Hill Cap Cloud Thuringia (HCCT) campaign. Cloud water was collected at the top of Mt. Schmücke while aerosol samples were collected at two stations upwind and downwind of Mt. Schmücke. Fourteen trace metals including Ti, V, Fe, Mn, Co, Zn, Ni, Cu, As, Sr, Rb, Pb, Cr, and Se were investigated during four full cloud events (FCEs) that fulfilled the conditions of a continuous air mass flow through the three stations. Aerosol particle trace metal concentrations were found to be lower than those observed in the same region during previous field experiments but were within a similar range to those observed in other rural regions in Europe. Fe and Zn were the most abundant elements with concentration ranges of 0.2–111.6 and 1.1–32.1 ng m−3, respectively. Fe, Mn, and Ti were mainly found in coarse mode aerosols while Zn, Pb, and As were mostly found in the fine mode. Correlation and enrichment factor analysis of trace metals revealed that trace metals such as Ti and Rb were mostly of crustal origin while trace metals such as Zn, Pb, As, Cr, Ni, V, and Cu were of anthropogenic origin. Trace metals such as Fe and Mn were of mixed origins including crustal and combustion sources. Trace metal cloud water concentration decreased from Ti, Mn, Cr, to Co with average concentrations of 9.18, 5.59, 5.54, and 0.46 μg L−1, respectively. A non-uniform distribution of soluble Fe, Cu, and Mn was observed across the cloud drop sizes. Soluble Fe and Cu were found mainly in cloud droplets with diameters between 16 and 22 μm, while Mn was found mostly in larger drops greater than 22 μm. Fe(III) was the main form of soluble Fe especially in the small and larger drops with concentrations ranging from 2.2 to 37.1 μg L−1. In contrast to other studies, Fe(II) was observed mainly in the evening hours, implying its presence was not directly related to photochemical processes. Aerosol–cloud interaction did not lead to a marked increase in soluble trace metal concentrations; rather it led to differences in the chemical composition of the aerosol due to preferential loss of aerosol particles through physical processes including cloud drop deposition to vegetative surfaces.
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Lachlan-Cope, Thomas, David C. S. Beddows, Neil Brough, Anna E. Jones, Roy M. Harrison, Angelo Lupi, Young Jun Yoon, Aki Virkkula y Manuel Dall'Osto. "On the annual variability of Antarctic aerosol size distributions at Halley Research Station". Atmospheric Chemistry and Physics 20, n.º 7 (17 de abril de 2020): 4461–76. http://dx.doi.org/10.5194/acp-20-4461-2020.
Resumen
Abstract. The Southern Ocean and Antarctic region currently best represent one of the few places left on our planet with conditions similar to the preindustrial age. Currently, climate models have a low ability to simulate conditions forming the aerosol baseline; a major uncertainty comes from the lack of understanding of aerosol size distributions and their dynamics. Contrasting studies stress that primary sea salt aerosol can contribute significantly to the aerosol population, challenging the concept of climate biogenic regulation by new particle formation (NPF) from dimethyl sulfide marine emissions. We present a statistical cluster analysis of the physical characteristics of particle size distributions (PSDs) collected at Halley (Antarctica) for the year 2015 (89 % data coverage; 6–209 nm size range; daily size resolution). By applying the Hartigan–Wong k-mean method we find eight clusters describing the entire aerosol population. Three clusters show pristine average low particle number concentrations (< 121–179 cm−3) with three main modes (30, 75–95 and 135–160 nm) and represent 57 % of the annual PSD (up to 89 %–100 % during winter and 34 %–65 % during summer based on monthly averages). Nucleation and Aitken mode PSD clusters dominate summer months (September–January, 59 %–90 %), whereas a clear bimodal distribution (43 and 134 nm, respectively; Hoppel minimum at mode 75 nm) is seen only during the December–April period (6 %–21 %). Major findings of the current work include: (1) NPF and growth events originate from both the sea ice marginal zone and the Antarctic plateau, strongly suggesting multiple vertical origins, including the marine boundary layer and free troposphere; (2) very low particle number concentrations are detected for a substantial part of the year (57 %), including summer (34 %–65 %), suggesting that the strong annual aerosol concentration cycle is driven by a short temporal interval of strong NPF events; (3) a unique pristine aerosol cluster is seen with a bimodal size distribution (75 and 160 nm, respectively), strongly associated with high wind speed and possibly associated with blowing snow and sea spray sea salt, dominating the winter aerosol population (34 %–54 %). A brief comparison with two other stations (Dome C – Concordia – and King Sejong Station) during the year 2015 (240 d overlap) shows that the dynamics of aerosol number concentrations and distributions are more complex than the simple sulfate–sea-spray binary combination, and it is likely that an array of additional chemical components and processes drive the aerosol population. A conceptual illustration is proposed indicating the various atmospheric processes related to the Antarctic aerosols, with particular emphasis on the origin of new particle formation and growth.
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Gerding, M., G. Baumgarten, U. Blum, J. P. Thayer, K. H. Fricke, R. Neuber y J. Fiedler. "Observation of an unusual mid-stratospheric aerosol layer in the Arctic: possible sources and implications for polar vortex dynamics". Annales Geophysicae 21, n.º 4 (30 de abril de 2003): 1057–69. http://dx.doi.org/10.5194/angeo-21-1057-2003.
Resumen
Abstract. By the beginning of winter 2000/2001, a mysterious stratospheric aerosol layer had been detected by four different Arctic lidar stations. The aerosol layer was observed first on 16 November 2000, at an altitude of about 38 km near Søndre Strømfjord, Greenland (67° N, 51° W) and on 19 November 2000, near Andenes, Norway (69° N, 16° E). Subsequently, in early December 2000, the aerosol layer was observed near Kiruna, Sweden (68° N, 21° E) and Ny-Ålesund, Spitsbergen (79° N, 12° E). No mid-latitude lidar station observed the presence of aerosols in this altitude region. The layer persisted throughout the winter 2000/2001, at least up to 12 February 2001. In November 2000, the backscatter ratio at a wavelength of 532 nm was up to 1.1, with a FWHM of about 2.5 km. By early February 2001, the layer had sedimented from an altitude of 38 km to about 26 km. Measurements at several wavelengths by the ALOMAR and Koldewey lidars indicate the particle size was between 30 and 50 nm. Depolarisation measurements reveal that the particles in the layer are aspherical, hence solid. In the mid-stratosphere, the ambient atmospheric temperature was too high to support in situ formation or existence of cloud particles consisting of ice or an acid-water solution. Furthermore, in the year 2000 there was no volcanic eruption, which could have injected aerosols into the upper stratosphere. Therefore, other origins of the aerosol, such as meteoroid debris, condensed rocket fuel, or aerosols produced under the influence of charged solar particles, will be discussed in the paper. Trajectory calculations illustrate the path of the aerosol cloud within the polar vortex and are used to link the observations at the different lidar sites. From the descent rate of the layer and particle sedimentation rates, the mean down-ward motion of air within the polar vortex was estimated to be about 124 m/d between 35 and 30 km, with higher values at the edge of the vortex.Key words. Atmospheric composition and structure (aerosols and particles; middle atmosphere composition and chemistry) – meteorology and atmospheric dynamics (middle atmosphere dynamics)
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Nemuc, A., J. Vasilescu, C. Talianu, L. Belegante y D. Nicolae. "Assessment of aerosol's mass concentrations from measured linear particle depolarization ratio (vertically resolved) and simulations". Atmospheric Measurement Techniques 6, n.º 11 (27 de noviembre de 2013): 3243–55. http://dx.doi.org/10.5194/amt-6-3243-2013.
Resumen
Abstract. Multi-wavelength depolarization Raman lidar measurements from Magurele, Romania are used in this study along with simulated mass-extinction efficiencies to calculate the mass concentration profiles of different atmospheric components, due to their different depolarization contribution to the 532 nm backscatter coefficient. Linear particle depolarization ratio (δpart) was computed using the relative amplification factor and the system-dependent molecular depolarization. The low depolarizing component was considered as urban/smoke, with a mean δpart of 3%, while for the high depolarizing component (mineral dust) a mean δpart of 35% was assumed. For this study 11 months of lidar measurements were analysed. Two study cases are presented in details: one for a typical Saharan dust aerosol intrusion, 10 June 2012 and one for 12 July 2012 when a lofted layer consisting of biomass burning smoke extended from 3 to 4.5 km height. Optical Properties of Aerosols and Clouds software package (OPAC) classification and conversion factors were used to calculate mass concentrations. We found that calibrated depolarization measurements are critical in distinguishing between smoke-reach aerosol during the winter and dust-reach aerosol during the summer, as well as between elevated aerosol layers having different origins. Good agreement was found between lidar retrievals and DREAM- Dust REgional Atmospheric Model forecasts in cases of Saharan dust. Our method was also compared against LIRIC (The Lidar/Radiometer Inversion Code) and very small differences were observed.
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Nemuc, A., J. Vasilescu, C. Talianu, L. Belegante y D. Nicolae. "Assessment of aerosol's mass concentrations from measured linear particle depolarization ratio (vertically resolved) and simulations". Atmospheric Measurement Techniques Discussions 6, n.º 3 (27 de junio de 2013): 5923–57. http://dx.doi.org/10.5194/amtd-6-5923-2013.
Resumen
Abstract. Multiwavelength depolarization Raman lidar measurements from Magurele, Romania are used in this study along with simulated mass-extinction efficiencies to calculate the mass concentrations profiles of different atmospheric components, due to their different depolarization contribution to the 532 nm backscatter coefficient. Linear particle depolarization ratio (δpart) was computed using the relative amplification factor and the system-dependent molecular depolarization. The low depolarizing component was considered as urban/smoke, with a mean δpart of 3%, while for the high depolarizing component (mineral dust) a mean δpart of 35% was assumed. For this study 11 months of lidar measurements were analyzed. Two study cases are presented in details: one for a typical Saharan dust aerosol intrusion, 10 June 2012 and one for 12 July 2012 when a lofted layer consisting of biomass burning smoke extended from 3 to 4.5 km height. Optical Properties of Aerosols and Clouds software package (OPAC) classification and conversion factors were used to calculate mass concentrations. We found that calibrated depolarization measurements are critical to distinguish between smoke-reach aerosol during the winter and dust-reach aerosol during the summer, as well as between elevated aerosol layers having different origins. Good agreement was found between lidar retrievals and DREAM- Dust REgional Atmospheric Model forecasts in cases of Saharan dust. Our method was also compared against LIRIC (The Lidar/Radiometer Inversion Code) and very small differences were observed.
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Diesch, J. M., F. Drewnick, S. R. Zorn, S. L. von der Weiden-Reinmüller, M. Martinez y S. Borrmann. "Variability of aerosol, gaseous pollutants and meteorological characteristics associated with changes in air mass origin at the SW Atlantic coast of Iberia". Atmospheric Chemistry and Physics 12, n.º 8 (25 de abril de 2012): 3761–82. http://dx.doi.org/10.5194/acp-12-3761-2012.
Resumen
Abstract. Measurements of the ambient aerosol were performed at the Southern coast of Spain, within the framework of the DOMINO (Diel Oxidant Mechanisms In relation to Nitrogen Oxides) project. The field campaign took place from 20 November until 9 December 2008 at the atmospheric research station "El Arenosillo" (37°5'47.76" N, 6°44'6.94" W). As the monitoring station is located at the interface between a natural park, industrial cities (Huelva, Seville) and the Atlantic Ocean, a variety of physical and chemical parameters of aerosols and gas phase could be characterized in dependency on the origin of air masses. Backwards trajectories were examined and compared with local meteorology to classify characteristic air mass types for several source regions. Aerosol number and mass as well as polycyclic aromatic hydrocarbons and black carbon concentrations were measured in PM1 and size distributions were registered covering a size range from 7 nm up to 32 μm. The chemical composition of the non-refractory submicron aerosol (NR-PM1) was measured by means of an Aerosol Mass Spectrometer (Aerodyne HR-ToF-AMS). Gas phase analyzers monitored various trace gases (O3, SO2, NO, NO2, CO2) and a weather station provided meteorological parameters. Lowest average submicron particle mass and number concentrations were found in air masses arriving from the Atlantic Ocean with values around 2 μg m−3 and 1000 cm−3. These mass concentrations were about two to four times lower than the values recorded in air masses of continental and urban origins. For some species PM1-fractions in marine air were significantly larger than in air masses originating from Huelva, a closely located city with extensive industrial activities. The largest fraction of sulfate (54%) was detected in marine air masses and was to a high degree not neutralized. In addition, small concentrations of methanesulfonic acid (MSA), a product of biogenic dimethyl sulfate (DMS) emissions, could be identified in the particle phase. In all air masses passing the continent the organic aerosol fraction dominated the total NR-PM1. For this reason, using Positive Matrix Factorization (PMF) four organic aerosol (OA) classes that can be associated with various aerosol sources and components were identified: a highly-oxygenated OA is the major component (43% OA) while semi-volatile OA accounts for 23%. A hydrocarbon-like OA mainly resulting from industries, traffic and shipping emissions as well as particles from wood burning emissions also contribute to total OA and depend on the air mass origin. A significant variability of ozone was observed that depends on the impact of different air mass types and solar radiation.
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Mei, Fan, Jian Wang, Shan Zhou, Qi Zhang, Sonya Collier y Jianzhong Xu. "Measurement report: Cloud condensation nuclei activity and its variation with organic oxidation level and volatility observed during an aerosol life cycle intensive operational period (ALC-IOP)". Atmospheric Chemistry and Physics 21, n.º 17 (2 de septiembre de 2021): 13019–29. http://dx.doi.org/10.5194/acp-21-13019-2021.
Resumen
Abstract. Cloud condensation nuclei (CCN) spectrum and the CCN activated fraction of size-resolved aerosols (SR-CCN) were measured at a rural site on Long Island during the Department of Energy (DOE) aerosol life cycle intensive operational period (ALC-IOP) from 15 July to 15 August 2011. During the last week of the ALC-IOP, the dependence of the activated fraction on aerosol volatility was characterized by sampling downstream of a thermodenuder (TD) operated at temperatures up to 100 ∘C. Here we present aerosol properties, including aerosol total number concentration, CCN spectrum, and the CCN hygroscopicity, for air masses of representative origins during the ALC-IOP. The hygroscopicity of organic species in the aerosol is derived from CCN hygroscopicity and chemical composition. The dependence of organic hygroscopicity on the organic oxidation level (e.g., atomic O:C ratio) agrees well with theoretical predictions and results from previous laboratory and field studies. The derived κorg and O:C ratio first increase as TD temperature increases from 20 ∘C (i.e., ambient temperature) to 50 or 75 ∘C and then decrease as TD temperature further increases to 100 ∘C. The initial increases of O:C and κorg with TD temperature below 50 ∘C are likely due to evaporation of more volatile organics with relatively lower O:C and hygroscopicity such as primary organic aerosol. At the high TD temperatures, the decreases of O:C and κorg indicate that evaporated organics were more oxygenated and had lower molecular weights. These trends are different from previous laboratory experiments and field observations, which reported that organic O:C increased monotonically with increasing TD temperature, whereas κorg decreased with the TD temperature. One possible reason is that previous studies were either focused on laboratory-generated secondary organic aerosol (SOA) or based on field observations at locations more dominated by SOA.
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Mogo, S., V. E. Cachorro, J. F. Lopez, E. Montilla, B. Torres, E. Rodríguez, Y. Bennouna y A. M. de Frutos. "In situ measurements of aerosols optical properties and number size distributions in a subarctic coastal region of Norway". Atmospheric Chemistry and Physics Discussions 11, n.º 12 (13 de diciembre de 2011): 32921–64. http://dx.doi.org/10.5194/acpd-11-32921-2011.
Resumen
Abstract. In situ measurements of aerosol optical properties were made in the summer of 2008 at the ALOMAR station facility (69°16 N, 16°00 E), located at a rural site in the north of the island of Andøya (Vesterålen archipelago), approximately 300 km north of the Arctic Circle. The extended three-month campaign was part of the POLARCAT Project (Polar Study using Aircraft, Remote Sensing, Surface Measurements and Models, of Climate, Chemistry, Aerosols, and Transport) of the International Polar Year (IPY-2007-2008). Its goal was to characterize the aerosols of this sub-Arctic area, which are frequently transported to the Arctic region. The ambient light-scattering coefficient, σs (550 nm), at ALOMAR had a measured hourly mean value of 5.41 Mm−1 (StD = 3.55 Mm−1), and the light-absorption coefficient, σa (550 nm), had a measured hourly mean value of 0.40 Mm−1 (StD = 0.27 Mm−1). The scattering/absorption Ångström exponents, αs,a, are used for a detailed analysis of the variations of the spectral shape of σs,a. Whereas αs demonstrates the presence of two particle sizes corresponding to two types of aerosols, the αa demonstrates only one type of absorbing aerosol particles. Values of αa above 1 were not observed. The single-scattering albedo, ω0, ranged from 0.62 to 0.99 (mean = 0.91, StD = 0.05), and the relationships of this property to the absorption/scattering coefficients and the Ångström exponents are presented. The concentration of the particles was monitored using a scanning mobility particle sizer (SMPS), an aerodynamic particle sizer (APS) and an ultrafine condensation particle counter (UCPC). The shape of the median size distribution of the particles in the submicrometer fraction was bimodal, and the submicrometer, micrometer and total concentrations presented hourly mean values of 1277 cm3 (StD = 1563 cm3), 1 cm3 (StD = 1 cm3) and 2463 cm3 (StD = 4251 cm3), respectively. The modal correlations were investigated, and the concentration of particles sized between 30 and 100 nm (Aitken mode) are presented as a function of the concentration of the particles sized between 100 and 390 nm (accumulation mode). The optical and the microphysical parameters are related to each other, and the results are presented. The origins and pathways of air masses were examined by computing the back-trajectories in a trajectory model (HYSPLIT). Six geographical sectors were defined to classify the air masses, and, based on the sector classification, the linkage between the air mass origin and the optical parameters was established. Aerosol size distributions were also evaluated in relation to the air masses. The relationships between the air mass origins and other parameters, especially those related to the single scattering albedo, allow us to describe two characteristic situations: northern and western air masses, which had predominantly marine aerosols, presented lower optical parameter values, indicating predominantly coarser and non-absorbent particles; and eastern and southern air masses, in which continental aerosols were predominant, presented higher values for all optical parameters, indicating the presence of smaller absorbent particles.
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Fuchs, Julia, Jan Cermak y Hendrik Andersen. "Building a cloud in the southeast Atlantic: understanding low-cloud controls based on satellite observations with machine learning". Atmospheric Chemistry and Physics 18, n.º 22 (22 de noviembre de 2018): 16537–52. http://dx.doi.org/10.5194/acp-18-16537-2018.
Resumen
Abstract. Understanding the processes that determine low-cloud properties and aerosol–cloud interactions (ACIs) is crucial for the estimation of their radiative effects. However, the covariation of meteorology and aerosols complicates the determination of cloud-relevant influences and the quantification of the aerosol–cloud relation. This study identifies and analyzes sensitivities of cloud fraction and cloud droplet effective radius to their meteorological and aerosol environment in the atmospherically stable southeast Atlantic during the biomass-burning season based on an 8-day-averaged data set. The effect of geophysical parameters on clouds is investigated based on a machine learning technique, gradient boosting regression trees (GBRTs), using a combination of satellite and reanalysis data as well as trajectory modeling of air-mass origins. A comprehensive, multivariate analysis of important drivers of cloud occurrence and properties is performed and evaluated. The statistical model reveals marked subregional differences of relevant drivers and processes determining low clouds in the southeast Atlantic. Cloud fraction is sensitive to changes of lower tropospheric stability in the oceanic, southwestern subregion, while in the northeastern subregion it is governed mostly by surface winds. In the pristine, oceanic subregion large-scale dynamics and aerosols seem to be more important for changes of cloud droplet effective radius than in the polluted, near-shore subregion, where free tropospheric temperature is more relevant. This study suggests the necessity to consider distinct ACI regimes in cloud studies in the southeast Atlantic.
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Han, Deming, Qingyan Fu, Song Gao, Li Li, Yingge Ma, Liping Qiao, Hao Xu et al. "Non-polar organic compounds in autumn and winter aerosols in a typical city of eastern China: size distribution and impact of gas–particle partitioning on PM<sub>2.5</sub> source apportionment". Atmospheric Chemistry and Physics 18, n.º 13 (4 de julio de 2018): 9375–91. http://dx.doi.org/10.5194/acp-18-9375-2018.
Resumen
Abstract. Aerosol-associated non-polar organic compounds (NPOCs), including 15 polycyclic aromatic hydrocarbons (PAHs), 30 n-alkanes, 2 iso-alkanes, 5 hopanes and 5 steranes, were identified and quantified in PM2.5 samples using the thermal desorption–gas chromatography–mass spectrometry (TD–GC–MS) method. The samples were mainly collected in autumn and winter in a typical city of eastern China. The total concentrations of NPOCs were 31.7–388.7 ng m−3, and n-alkanes were the most abundant species (67.2 %). The heavy-molecular-weight PAHs (four- and five-ring) contributed 67.9 % of the total PAHs, and the middle-chain-length n-alkanes (C25–C34) were the most abundant (72.3 %) in n-alkanes. PAHs and n-alkanes were mainly distributed in the 0.56–1.00 µm fraction, while ∑ (hopanes + steranes) were associated with the 0.32–1.00 µm fraction, suggesting condensation of combustion products was their important origin. The ratio–ratio plots indicated that NPOCs in the local area were affected by photochemical degradation. To reduce the uncertainty caused by only particle NPOC data for source apportionment, the particle and predicted gaseous-phase NPOCs, incorporated with other PM2.5 compound were used as input data for the positive matrix factorization (PMF) model. Eight factors were extracted for both cases: secondary aerosol formation, vehicle exhaust, industrial emission, coal combustion, biomass burning, ship emission, and dust and light NPOCs. These findings highlight the emissions from different aerosol-associated NPOC origins, which caused different size-specific distributions, photodegradation and gas–particle partitioning, which further affect PM2.5 source apportionment. Considering these effects on organic tracers will help us accurately identify the potential sources of aerosols and then asses the contributions from each source.
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Lewis, C. W. y W. Einfeld. "Origins of carbonaceous aerosol in Denver and Albuquerque during winter". Environment International 11, n.º 2-4 (enero de 1985): 243–47. http://dx.doi.org/10.1016/0160-4120(85)90016-9.
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Bressi, M., J. Sciare, V. Ghersi, N. Mihalopoulos, J. E. Petit, J. B. Nicolas, S. Moukhtar et al. "Sources and geographical origins of fine aerosols in Paris (France)". Atmospheric Chemistry and Physics 14, n.º 16 (27 de agosto de 2014): 8813–39. http://dx.doi.org/10.5194/acp-14-8813-2014.
Resumen
Abstract. The present study aims at identifying and apportioning fine aerosols to their major sources in Paris (France) – the second most populated "larger urban zone" in Europe – and determining their geographical origins. It is based on the daily chemical composition of PM2.5 examined over 1 year at an urban background site of Paris (Bressi et al., 2013). Positive matrix factorization (EPA PMF3.0) was used to identify and apportion fine aerosols to their sources; bootstrapping was performed to determine the adequate number of PMF factors, and statistics (root mean square error, coefficient of determination, etc.) were examined to better model PM2.5 mass and chemical components. Potential source contribution function (PSCF) and conditional probability function (CPF) allowed the geographical origins of the sources to be assessed; special attention was paid to implement suitable weighting functions. Seven factors, namely ammonium sulfate (A.S.)-rich factor, ammonium nitrate (A.N.)-rich factor, heavy oil combustion, road traffic, biomass burning, marine aerosols and metal industry, were identified; a detailed discussion of their chemical characteristics is reported. They contribute 27, 24, 17, 14, 12, 6 and 1% of PM2.5 mass (14.7 μg m−3) respectively on the annual average; their seasonal variability is discussed. The A.S.- and A.N.-rich factors have undergone mid- or long-range transport from continental Europe; heavy oil combustion mainly stems from northern France and the English Channel, whereas road traffic and biomass burning are primarily locally emitted. Therefore, on average more than half of PM2.5 mass measured in the city of Paris is due to mid- or long-range transport of secondary aerosols stemming from continental Europe, whereas local sources only contribute a quarter of the annual averaged mass. These results imply that fine-aerosol abatement policies conducted at the local scale may not be sufficient to notably reduce PM2.5 levels at urban background sites in Paris, suggesting instead more coordinated strategies amongst neighbouring countries. Similar conclusions might be drawn in other continental urban background sites given the transboundary nature of PM2.5 pollution.
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Jang, Kyoung-Soon, A. Young Choi, Mira Choi, Hyunju Kang, Tae-Wook Kim y Ki-Tae Park. "Size-Segregated Chemical Compositions of HULISs in Ambient Aerosols Collected during the Winter Season in Songdo, South Korea". Atmosphere 10, n.º 4 (25 de abril de 2019): 226. http://dx.doi.org/10.3390/atmos10040226.
Resumen
The primary objective of this study was to investigate the molecular compositions of humic-like substances (HULISs) in size-resolved ambient aerosols, which were collected using an Anderson-type air sampler (eight size cuts between 0.43 and 11 μm) during the winter season (i.e., the heating period of 8–12 January 2018) in Songdo, South Korea. The aerosol samples collected during the pre- (preheating, 27 November–1 December 2017) and post-winter (postheating, 12–16 March 2018) periods were used as controls for the winter season samples. According to the concentrations of the chromophoric organics determined at an ultraviolet (UV) wavelength of 305 nm, most of the HULIS compounds were found to be predominantly enriched in particles less than 2.1 μm regardless of the sampling period, which shows that particulate matter (diameter less than 2.5 μm; PM2.5) aerosols were the dominant carriers of airborne organics. Ultrahigh-resolution Fourier transform ion cyclotron resonance mass spectrometry (UHR FT–ICR MS) analysis of the aerosol-carried organic substances revealed that as the aerosol size increased the proportions of CHO and nitrogen-containing CHO (CHON) compounds decreased, while the proportion of sulfur-containing CHO (CHOS) species increased. In particular, the ambient aerosols during the heating period seemed to present more CHO and CHON and less CHOS molecules compared to aerosols collected during the pre- and postheating periods. The aerosols collected during the heating period also exhibited more aromatic nitrogen-containing compounds, which may have originated from primary combustion processes. Overall, the particle size distribution was likely influenced by source origins; smaller particles are likely from local sources, such as traffic and industries, and larger particles (i.e., aged particles) are likely derived from long-range transport generating secondary organic aerosols (SOAs) in the atmosphere. The results of the size-segregated particles can be utilized to understand particle formation mechanisms and shed light on their toxicity to human health.
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Val Martin, M., C. L. Heald, B. Ford, A. J. Prenni y C. Wiedinmyer. "A decadal satellite analysis of the origins and impacts of smoke in Colorado". Atmospheric Chemistry and Physics Discussions 13, n.º 3 (26 de marzo de 2013): 8233–60. http://dx.doi.org/10.5194/acpd-13-8233-2013.
Resumen
Abstract. We analyze the record of aerosol optical depth (AOD) measured by the MODerate resolution Imaging Spectroradiometer (MODIS) aboard the Terra satellite in combination with surface PM2.5 to investigate the impact of fires on aerosol loading and air quality over Colorado from 2000 to 2012, and to evaluate the contribution of local versus transported smoke. Fire smoke contributed significantly to the AOD levels observed over Colorado. During the worst fire seasons of 2002 and 2012, average MODIS AOD over the Colorado Front Range corridor were 20–50% larger than the other 11 yr studied. Surface PM2.5 was also unusually elevated during fire events and concentrations were in many occasions above the daily National Ambient Air Quality Standard (35 μg m−3) and even reached locally unhealthy levels (> 100 μg m−3) over populated areas during the 2012 High Park fire and the 2002 Hayman fire. Over the 13 yr examined, long-range transport of smoke from northwestern US and even California (>1500 km distance) occurred often and affected AOD and surface PM2.5. During most of the transport events, MODIS AOD and surface PM2.5 were reasonable correlated (r2 = 0.2–0.9), indicating that smoke subsided into the Colorado boundary layer and reached surface levels. However, that is not always the case since at least one event of AOD enhancement was disconnected from the surface (r2<0.01 and low PM2.5 levels). Observed plume heights from the Multi-angle Imaging SpectroRadiometer (MISR) satellite instrument and vertical aerosol profiles measured by the space-based Cloud-Aerosol LIdar with Orthogonal Polarization (CALIOP) showed a complex vertical distribution of smoke emitted by the High Park fire in 2012. Smoke was detected from a range of 1.5 to 7.5 km altitude at the fire origin and from ground levels to 12.3 km altitude far away from the source. The variability of smoke altitude as well as the local meteorology were key in determining the aerosol loading and air quality over the Colorado Front Range region. Our results underline the importance of accurate characterization of the vertical distribution of smoke for estimating the air quality degradation associated with fire activity and its link to human health.
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Val Martin, M., C. L. Heald, B. Ford, A. J. Prenni y C. Wiedinmyer. "A decadal satellite analysis of the origins and impacts of smoke in Colorado". Atmospheric Chemistry and Physics 13, n.º 15 (2 de agosto de 2013): 7429–39. http://dx.doi.org/10.5194/acp-13-7429-2013.
Resumen
Abstract. We analyze the record of aerosol optical depth (AOD) measured by the MODerate resolution Imaging Spectroradiometer (MODIS) aboard the Terra satellite in combination with surface PM2.5 to investigate the impact of fires on aerosol loading and air quality over Colorado from 2000 to 2012, and to evaluate the contribution of local versus transported smoke. Fire smoke contributed significantly to the AOD levels observed over Colorado. During the worst fire seasons of 2002 and 2012, average MODIS AOD over the Colorado Front Range corridor were 20–50% larger than the other 11 yr studied. Surface PM2.5 was also unusually elevated during fire events and concentrations were in many occasions above the daily National Ambient Air Quality Standard (35 μg m−3) and even reached locally unhealthy levels (> 100 μg m−3) over populated areas during the 2012 High Park fire and the 2002 Hayman fire. Over the 13 yr examined, long-range transport of smoke from northwestern US and even California (> 1500 km distance) occurred often and affected AOD and surface PM2.5. During most of the transport events, MODIS AOD and surface PM2.5 were reasonable correlated (r2 = 0.2–0.9), indicating that smoke subsided into the Colorado boundary layer and reached surface levels. However, that is not always the case since at least one event of AOD enhancement was disconnected from the surface (r2<0.01 and low PM2.5 levels). Observed plume heights from the Multi-angle Imaging SpectroRadiometer (MISR) satellite instrument and vertical aerosol profiles measured by the space-based Cloud-Aerosol LIdar with Orthogonal Polarization (CALIOP) showed a complex vertical distribution of smoke emitted by the High Park fire in 2012. Smoke was detected from a range of 1.5 to 7.5 km altitude at the fire origin and from ground levels to 12.3 km altitude far away from the source. The variability of smoke altitude as well as the local meteorology were key in determining the aerosol loading and air quality over the Colorado Front Range region. Our results underline the importance of accurate characterization of the vertical distribution of smoke for estimating the air quality degradation associated with fire activity and its link to human health.
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Dall'Osto, M. y R. M. Harrison. "Urban organic aerosols measured by single particle mass spectrometry in the megacity of London". Atmospheric Chemistry and Physics 12, n.º 9 (10 de mayo de 2012): 4127–42. http://dx.doi.org/10.5194/acp-12-4127-2012.
Resumen
Abstract. During the month of October 2006, as part of the REPARTEE-I experiment (Regent's Park and Tower Environmental Experiment) an Aerosol Time-Of-Flight Mass Spectrometer (ATOFMS) was deployed at an urban background location in the city of London, UK. Fifteen particle types were classified, some of which were already discussed (Dall'Osto et al., 2009a,b; Harrison et al., 2012). In this manuscript the origins and properties of four unreported particle types postulated to be due to locally generated aerosols, independent of the air mass type advected into London, are examined. One particle type, originating from lubricating oil (referred to as Ca-EC), was associated with morning rush hour traffic emissions. A second particle type, composed of both inorganic and organic species (called Na-EC-OC), was found enhanced in particle number concentration during evening time periods, and is likely to originate from a source operating at this time of day, or more probably from condensation of semi-volatile species. A third class, internally mixed with organic carbon and sulphate (called OC), was found to spike both in the morning and evenings although it could not unambiguously associated with a specific source or atmospheric process. The fourth class (Secondary Organic Aerosols – Polycyclic Aromatic Hydrocarbon; SOA-PAH) exhibited maximum frequency during the warmest part of the day, and a number of factors point towards secondary aerosol production from traffic-related volatile aromatic compounds. Single particle mass spectra of this particle type showed an oxidized polycyclic aromatic compound signature. A comparison of ATOFMS particle class data is then made with factors obtained by Positive Matrix Factorization and PAH signatures obtained from Aerosol Mass Spectrometer (AMS) data (Allan et al., 2010). Both the Ca-EC and OC particle types correlate with primary Hydrocarbon-like Organic Aerosol (HOA, R2 = 0.65 and 0.50 respectively), and Na-EC-OC correlates weakly with the AMS secondary Oxygenated Organic Aerosol (OOA), (R2 = 0.35). Cluster SOA-PAH was found not to correlate with any AMS signal. A detailed analysis was conducted to identify ATOFMS particle type(s) representative of the AMS cooking aerosol factor (COA), but no convincing associations were found. The combined ATOFMS and AMS results of this REPARTEE study do not always provide an entirely coherent interpretation.
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Diesch, J. M., F. Drewnick, S. R. Zorn, S. L. von der Weiden-Reinmüller, M. Martinez y S. Borrmann. "Variability of aerosol, gaseous pollutants and meteorological characteristics associated with continental, urban and marine air masses at the SW Atlantic coast of Iberia". Atmospheric Chemistry and Physics Discussions 11, n.º 12 (2 de diciembre de 2011): 31585–642. http://dx.doi.org/10.5194/acpd-11-31585-2011.
Resumen
Abstract. Measurements of the ambient aerosol were performed at the Southern coast of Spain, within the framework of the DOMINO (Diel Oxidant Mechanisms In relation to Nitrogen Oxides) project. The field campaign took place from 20 November until 9 December 2008 at the atmospheric research station "El Arenosillo" (37°5'47.76" N, 6&deg44'6.94" W). As the monitoring station is located at the interface between a natural park, industrial cities (Huelva, Seville) and the Atlantic Ocean a variety of physical and chemical parameters of aerosols and gas phase could be characterized in dependency on the origin of air masses. Backwards trajectories were examined and compared with local meteorology to classify characteristic air mass types for several source regions. Aerosol number and mass as well as polycyclic aromatic hydrocarbons and black carbon concentrations were measured in PM1 and size distributions were registered covering a size range from 7 nm up to 32 μm. The chemical composition of the non-refractory submicron aerosol was measured by means of an Aerosol Mass Spectrometer (Aerodyne HR-ToF-AMS). Gas phase analyzers monitored various trace gases (O3, SO2, NO, NO2, CO2) and a weather station provided meteorological parameters. Lowest average submicron particle mass and number concentrations were found in air masses arriving from the Atlantic Ocean with values around 2 μg m−3 and 1000 cm−3. These mass concentrations were about two to four times lower than the values recorded in air masses of continental and urban origins. For some species PM1-fractions in marine air were significantly larger than in air masses originating from Huelva, a closely located city with extensive industrial activities. The largest fraction of sulfate (54%) was detected in marine air masses and was to a high degree not neutralized. In addition small concentrations of methanesulfonic acid (MSA), a product of biogenic dimethyl sulfate (DMS) emissions could be identified in the particle phase. In all air masses passing the continent the organic aerosol fraction dominated the total NR-PM1. For this reason, using Positive Matrix Factorization (PMF) four organic aerosol (OA) classes that can be associated with various aerosol sources and components were identified: a highly-oxygenated OA is the major component contributing an average of 43% of the particulate organic mass while the semi-volatile OA accounts for 23%. A hydrocarbon-like OA mainly resulting from industries, traffic and shipping emissions as well as particles from wood burning emissions also contribute to total OA dependent on the air mass origin. The variability of ozone is not only affected by different types of air masses but also significantly by the diurnal variation as a consequence of the solar radiation as well as local meteorological parameters.
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Deng, Chenjuan, Yiran Li, Chao Yan, Jin Wu, Runlong Cai, Dongbin Wang, Yongchun Liu et al. "Measurement report: Size distributions of urban aerosols down to 1 nm from long-term measurements". Atmospheric Chemistry and Physics 22, n.º 20 (19 de octubre de 2022): 13569–80. http://dx.doi.org/10.5194/acp-22-13569-2022.
Resumen
Abstract. The size distributions of urban atmospheric aerosols convey important information on their origins and impacts. Their long-term characteristics, especially for sub-3 nm particles, are still limited. In this study, we examined the characteristics of atmospheric aerosol size distributions down to ∼1 nm based on 4-year measurements in urban Beijing. Using cluster analysis, three typical types of number size distributions were identified, i.e., daytime new particle formation (NPF) type, daytime non-NPF type, and nighttime type. Combining a power law distribution and multiple lognormal distributions can well represent the sharp concentration decrease of sub-3 nm particles with increasing size and the modal characteristics for those above 3 nm in the submicron size range. The daytime NPF type exhibits high concentrations of sub-3 nm aerosols together with other three modes. However, both the daytime non-NPF type and the nighttime type have a low abundance of sub-3 nm aerosol particles together with only two distinct modes. In urban Beijing, the concentration of H2SO4 monomer during the daytime with NPF is similar to that during the daytime without NPF, while significantly higher than that during the nighttime. The concentration of atmospheric sub-3 nm particles on NPF days has a strong seasonality while their seasonality on non-NPF days is less pronounced. In addition to NPF as the most important source, we show that vehicles can emit sub-3 nm particles as well, although their influence on the measured aerosol population strongly depends on the distance from the road.