Articles | Volume 18, issue 17
https://doi.org/10.5194/acp-18-13215-2018
© Author(s) 2018. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/acp-18-13215-2018
© Author(s) 2018. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Research article
| 
13 Sep 2018
Research article |
| 13 Sep 2018
| 13 Sep 2018
Source apportionment of atmospheric aerosol in a marine dusty environment by ionic/composition mass balance (IMB)
João Cardoso
CESAM & Dep. Environ, Aveiro University, Aveiro, Portugal
Department of Science and Technology, Cape Verde University, Praia, Cabo Verde
Susana M. Almeida
TN, Instituto Superior Técnico, Lisbon University,
Bobadela, Portugal
Teresa Nunes
CESAM & Dep. Environ, Aveiro University, Aveiro, Portugal
Marina Almeida-Silva
TN, Instituto Superior Técnico, Lisbon University,
Bobadela, Portugal
Mário Cerqueira
CESAM & Dep. Environ, Aveiro University, Aveiro, Portugal
Célia Alves
CESAM & Dep. Environ, Aveiro University, Aveiro, Portugal
Fernando Rocha
Geobiotec & Dep. Geosciences, Aveiro University, Aveiro, Portugal
Paula Chaves
TN, Instituto Superior Técnico, Lisbon University,
Bobadela, Portugal
Miguel Reis
TN, Instituto Superior Técnico, Lisbon University,
Bobadela, Portugal
Pedro Salvador
Environ Dep, CIEMAT, Madrid, Spain
Begoña Artiñano
Environ Dep, CIEMAT, Madrid, Spain
Casimiro Pio
CORRESPONDING AUTHOR
CESAM & Dep. Environ, Aveiro University, Aveiro, Portugal
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Guilherme Martins Pereira, Leonardo Yoshiaki Kamigauti, Rubens Fabio Pereira, Djacinto Monteiro dos Santos, Thayná da Silva Santos, José Vinicius Martins, Célia Alves, Cátia Gonçalves, Ismael Casotti Rienda, Nora Kováts, Thiago Nogueira, Luciana Rizzo, Paulo Artaxo, Regina Maura de Miranda, Marcia Akemi Yamasoe, Edmilson Dias de Freitas, Pérola de Castro Vasconcellos, and Maria de Fatima Andrade
EGUsphere, https://doi.org/10.5194/egusphere-2024-2212, https://doi.org/10.5194/egusphere-2024-2212, 2024
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The chemical composition of fine particulate matter was studied in the megacity of São Paulo (Brazil) during a polluted period. Vehicular-related sources were dominant; however, a high contribution of biomass burning was observed and correlated with sample ecotoxicity. Emerging biomass burning sources, such as forest fires and sugarcane bagasse-based power plants, highlight the need for additional control measures alongside stricter rules concerning vehicular emissions.
Natalie M. Mahowald, Longlei Li, Julius Vira, Marje Prank, Douglas S. Hamilton, Hitoshi Matsui, Ron L. Miller, Louis Lu, Ezgi Akyuz, Daphne Meidan, Peter G. Hess, Heikki Lihavainen, Christine Wiedinmyer, Jenny Hand, Maria Grazia Alaimo, Célia Alves, Andres Alastuey, Paulo Artaxo, Africa Barreto, Francisco Barraza, Silvia Becagli, Giulia Calzolai, Shankararaman Chellam, Ying Chen, Patrick Chuang, David D. Cohen, Cristina Colombi, Evangelia Diapouli, Gaetano Dongarra, Konstantinos Eleftheriadis, Johann Engelbrecht, Corinne Galy-Lacaux, Cassandra Gaston, Dario Gomez, Yenny González Ramos, Roy M. Harrison, Chris Heyes, Barak Herut, Philip Hopke, Christoph Hüglin, Maria Kanakidou, Zsofia Kertesz, Zbigniew Klimont, Katriina Kyllönen, Fabrice Lambert, Xiaohong Liu, Remi Losno, Franco Lucarelli, Willy Maenhaut, Beatrice Marticorena, Randall V. Martin, Nikolaos Mihalopoulos, Yasser Morera-Gomez, Adina Paytan, Joseph Prospero, Sergio Rodríguez, Patricia Smichowski, Daniela Varrica, Brenna Walsh, Crystal Weagle, and Xi Zhao
EGUsphere, https://doi.org/10.5194/egusphere-2024-1617, https://doi.org/10.5194/egusphere-2024-1617, 2024
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Aerosol particles are an important part of the Earth system, but their concentrations are spatially and temporally heterogeneous, as well as variable in size and composition. Here we present a new compilation of PM2.5 and PM10 aerosol observations, focusing on the spatial variability across different observational stations, including composition, and demonstrate a method for comparing the datasets to model output.
Natalie M. Mahowald, Longlei Li, Julius Vira, Marje Prank, Douglas S. Hamilton, Hitoshi Matsui, Ron L. Miller, Louis Lu, Ezgi Akyuz, Daphne Meidan, Peter Hess, Heikki Lihavainen, Christine Wiedinmyer, Jenny Hand, Maria Grazia Alaimo, Célia Alves, Andres Alastuey, Paulo Artaxo, Africa Barreto, Francisco Barraza, Silvia Becagli, Giulia Calzolai, Shankarararman Chellam, Ying Chen, Patrick Chuang, David D. Cohen, Cristina Colombi, Evangelia Diapouli, Gaetano Dongarra, Konstantinos Eleftheriadis, Corinne Galy-Lacaux, Cassandra Gaston, Dario Gomez, Yenny González Ramos, Hannele Hakola, Roy M. Harrison, Chris Heyes, Barak Herut, Philip Hopke, Christoph Hüglin, Maria Kanakidou, Zsofia Kertesz, Zbiginiw Klimont, Katriina Kyllönen, Fabrice Lambert, Xiaohong Liu, Remi Losno, Franco Lucarelli, Willy Maenhaut, Beatrice Marticorena, Randall V. Martin, Nikolaos Mihalopoulos, Yasser Morera-Gomez, Adina Paytan, Joseph Prospero, Sergio Rodríguez, Patricia Smichowski, Daniela Varrica, Brenna Walsh, Crystal Weagle, and Xi Zhao
Earth Syst. Sci. Data Discuss., https://doi.org/10.5194/essd-2024-1, https://doi.org/10.5194/essd-2024-1, 2024
Preprint withdrawn
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Aerosol particles can interact with incoming solar radiation and outgoing long wave radiation, change cloud properties, affect photochemistry, impact surface air quality, and when deposited impact surface albedo of snow and ice, and modulate carbon dioxide uptake by the land and ocean. Here we present a new compilation of aerosol observations including composition, a methodology for comparing the datasets to model output, and show the implications of these results using one model.
María Ángeles López-Cayuela, Carmen Córdoba-Jabonero, Diego Bermejo-Pantaleón, Michaël Sicard, Vanda Salgueiro, Francisco Molero, Clara Violeta Carvajal-Pérez, María José Granados-Muñoz, Adolfo Comerón, Flavio T. Couto, Rubén Barragán, María-Paz Zorzano, Juan Antonio Bravo-Aranda, Constantino Muñoz-Porcar, María João Costa, Begoña Artíñano, Alejandro Rodríguez-Gómez, Daniele Bortoli, Manuel Pujadas, Jesús Abril-Gago, Lucas Alados-Arboledas, and Juan Luis Guerrero-Rascado
Atmos. Chem. Phys., 23, 143–161, https://doi.org/10.5194/acp-23-143-2023, https://doi.org/10.5194/acp-23-143-2023, 2023
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An intense Saharan dust outbreak crossing the Iberian Peninsula in springtime was monitored to determinine the specific contribution of fine and coarse dust particles at five lidar stations, strategically covering its SW–central–NE pathway. Expected dust ageing along the transport started unappreciated. A different fine-dust impact on optical (~30 %) and mass (~10 %) properties was found. Use of polarized lidar measurements (mainly in elastic systems) for fine/coarse dust separation is crucial.
Clémence Rose, Martine Collaud Coen, Elisabeth Andrews, Yong Lin, Isaline Bossert, Cathrine Lund Myhre, Thomas Tuch, Alfred Wiedensohler, Markus Fiebig, Pasi Aalto, Andrés Alastuey, Elisabeth Alonso-Blanco, Marcos Andrade, Begoña Artíñano, Todor Arsov, Urs Baltensperger, Susanne Bastian, Olaf Bath, Johan Paul Beukes, Benjamin T. Brem, Nicolas Bukowiecki, Juan Andrés Casquero-Vera, Sébastien Conil, Konstantinos Eleftheriadis, Olivier Favez, Harald Flentje, Maria I. Gini, Francisco Javier Gómez-Moreno, Martin Gysel-Beer, Anna Gannet Hallar, Ivo Kalapov, Nikos Kalivitis, Anne Kasper-Giebl, Melita Keywood, Jeong Eun Kim, Sang-Woo Kim, Adam Kristensson, Markku Kulmala, Heikki Lihavainen, Neng-Huei Lin, Hassan Lyamani, Angela Marinoni, Sebastiao Martins Dos Santos, Olga L. Mayol-Bracero, Frank Meinhardt, Maik Merkel, Jean-Marc Metzger, Nikolaos Mihalopoulos, Jakub Ondracek, Marco Pandolfi, Noemi Pérez, Tuukka Petäjä, Jean-Eudes Petit, David Picard, Jean-Marc Pichon, Veronique Pont, Jean-Philippe Putaud, Fabienne Reisen, Karine Sellegri, Sangeeta Sharma, Gerhard Schauer, Patrick Sheridan, James Patrick Sherman, Andreas Schwerin, Ralf Sohmer, Mar Sorribas, Junying Sun, Pierre Tulet, Ville Vakkari, Pieter Gideon van Zyl, Fernando Velarde, Paolo Villani, Stergios Vratolis, Zdenek Wagner, Sheng-Hsiang Wang, Kay Weinhold, Rolf Weller, Margarita Yela, Vladimir Zdimal, and Paolo Laj
Atmos. Chem. Phys., 21, 17185–17223, https://doi.org/10.5194/acp-21-17185-2021, https://doi.org/10.5194/acp-21-17185-2021, 2021
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Aerosol particles are a complex component of the atmospheric system the effects of which are among the most uncertain in climate change projections. Using data collected at 62 stations, this study provides the most up-to-date picture of the spatial distribution of particle number concentration and size distribution worldwide, with the aim of contributing to better representation of aerosols and their interactions with clouds in models and, therefore, better evaluation of their impact on climate.
Paolo Laj, Alessandro Bigi, Clémence Rose, Elisabeth Andrews, Cathrine Lund Myhre, Martine Collaud Coen, Yong Lin, Alfred Wiedensohler, Michael Schulz, John A. Ogren, Markus Fiebig, Jonas Gliß, Augustin Mortier, Marco Pandolfi, Tuukka Petäja, Sang-Woo Kim, Wenche Aas, Jean-Philippe Putaud, Olga Mayol-Bracero, Melita Keywood, Lorenzo Labrador, Pasi Aalto, Erik Ahlberg, Lucas Alados Arboledas, Andrés Alastuey, Marcos Andrade, Begoña Artíñano, Stina Ausmeel, Todor Arsov, Eija Asmi, John Backman, Urs Baltensperger, Susanne Bastian, Olaf Bath, Johan Paul Beukes, Benjamin T. Brem, Nicolas Bukowiecki, Sébastien Conil, Cedric Couret, Derek Day, Wan Dayantolis, Anna Degorska, Konstantinos Eleftheriadis, Prodromos Fetfatzis, Olivier Favez, Harald Flentje, Maria I. Gini, Asta Gregorič, Martin Gysel-Beer, A. Gannet Hallar, Jenny Hand, Andras Hoffer, Christoph Hueglin, Rakesh K. Hooda, Antti Hyvärinen, Ivo Kalapov, Nikos Kalivitis, Anne Kasper-Giebl, Jeong Eun Kim, Giorgos Kouvarakis, Irena Kranjc, Radovan Krejci, Markku Kulmala, Casper Labuschagne, Hae-Jung Lee, Heikki Lihavainen, Neng-Huei Lin, Gunter Löschau, Krista Luoma, Angela Marinoni, Sebastiao Martins Dos Santos, Frank Meinhardt, Maik Merkel, Jean-Marc Metzger, Nikolaos Mihalopoulos, Nhat Anh Nguyen, Jakub Ondracek, Noemi Pérez, Maria Rita Perrone, Jean-Eudes Petit, David Picard, Jean-Marc Pichon, Veronique Pont, Natalia Prats, Anthony Prenni, Fabienne Reisen, Salvatore Romano, Karine Sellegri, Sangeeta Sharma, Gerhard Schauer, Patrick Sheridan, James Patrick Sherman, Maik Schütze, Andreas Schwerin, Ralf Sohmer, Mar Sorribas, Martin Steinbacher, Junying Sun, Gloria Titos, Barbara Toczko, Thomas Tuch, Pierre Tulet, Peter Tunved, Ville Vakkari, Fernando Velarde, Patricio Velasquez, Paolo Villani, Sterios Vratolis, Sheng-Hsiang Wang, Kay Weinhold, Rolf Weller, Margarita Yela, Jesus Yus-Diez, Vladimir Zdimal, Paul Zieger, and Nadezda Zikova
Atmos. Meas. Tech., 13, 4353–4392, https://doi.org/10.5194/amt-13-4353-2020, https://doi.org/10.5194/amt-13-4353-2020, 2020
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The paper establishes the fiducial reference of the GAW aerosol network providing the fully characterized value chain to the provision of four climate-relevant aerosol properties from ground-based sites. Data from almost 90 stations worldwide are reported for a reference year, 2017, providing a unique and very robust view of the variability of these variables worldwide. Current gaps in the GAW network are analysed and requirements for the Global Climate Monitoring System are proposed.
Marco Pandolfi, Lucas Alados-Arboledas, Andrés Alastuey, Marcos Andrade, Christo Angelov, Begoña Artiñano, John Backman, Urs Baltensperger, Paolo Bonasoni, Nicolas Bukowiecki, Martine Collaud Coen, Sébastien Conil, Esther Coz, Vincent Crenn, Vadimas Dudoitis, Marina Ealo, Kostas Eleftheriadis, Olivier Favez, Prodromos Fetfatzis, Markus Fiebig, Harald Flentje, Patrick Ginot, Martin Gysel, Bas Henzing, Andras Hoffer, Adela Holubova Smejkalova, Ivo Kalapov, Nikos Kalivitis, Giorgos Kouvarakis, Adam Kristensson, Markku Kulmala, Heikki Lihavainen, Chris Lunder, Krista Luoma, Hassan Lyamani, Angela Marinoni, Nikos Mihalopoulos, Marcel Moerman, José Nicolas, Colin O'Dowd, Tuukka Petäjä, Jean-Eudes Petit, Jean Marc Pichon, Nina Prokopciuk, Jean-Philippe Putaud, Sergio Rodríguez, Jean Sciare, Karine Sellegri, Erik Swietlicki, Gloria Titos, Thomas Tuch, Peter Tunved, Vidmantas Ulevicius, Aditya Vaishya, Milan Vana, Aki Virkkula, Stergios Vratolis, Ernest Weingartner, Alfred Wiedensohler, and Paolo Laj
Atmos. Chem. Phys., 18, 7877–7911, https://doi.org/10.5194/acp-18-7877-2018, https://doi.org/10.5194/acp-18-7877-2018, 2018
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This investigation presents the variability in near-surface in situ aerosol particle light-scattering measurements obtained over the past decade at 28 measuring atmospheric observatories which are part of the ACTRIS Research Infrastructure, and most of them belong to the GAW network. This paper provides a comprehensive picture of the spatial and temporal variability of aerosol particles optical properties in Europe.
Andrés Esteban Bedoya-Velásquez, Francisco Navas-Guzmán, María José Granados-Muñoz, Gloria Titos, Roberto Román, Juan Andrés Casquero-Vera, Pablo Ortiz-Amezcua, Jose Antonio Benavent-Oltra, Gregori de Arruda Moreira, Elena Montilla-Rosero, Carlos David Hoyos, Begoña Artiñano, Esther Coz, Francisco José Olmo-Reyes, Lucas Alados-Arboledas, and Juan Luis Guerrero-Rascado
Atmos. Chem. Phys., 18, 7001–7017, https://doi.org/10.5194/acp-18-7001-2018, https://doi.org/10.5194/acp-18-7001-2018, 2018
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This study focuses on the analysis of aerosol hygroscopic growth during the SLOPE I campaign combining active and passive remote sensors at ACTRIS Granada station and in situ instrumentation at a mountain station (Sierra Nevada station, SNS). The results showed good agreement on gamma parameters by using remote sensing with respect to those calculated using Mie theory at SNS, with relative differences lower than 9 % at 532 nm and 11 % at 355 nm.
Xavier Querol, Andrés Alastuey, Gotzon Gangoiti, Noemí Perez, Hong K. Lee, Heeram R. Eun, Yonghee Park, Enrique Mantilla, Miguel Escudero, Gloria Titos, Lucio Alonso, Brice Temime-Roussel, Nicolas Marchand, Juan R. Moreta, M. Arantxa Revuelta, Pedro Salvador, Begoña Artíñano, Saúl García dos Santos, Mónica Anguas, Alberto Notario, Alfonso Saiz-Lopez, Roy M. Harrison, Millán Millán, and Kang-Ho Ahn
Atmos. Chem. Phys., 18, 6511–6533, https://doi.org/10.5194/acp-18-6511-2018, https://doi.org/10.5194/acp-18-6511-2018, 2018
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We show the main drivers of high O3 episodes in and around Madrid. High levels of ultrafine particles (UFPs) are evidenced, but we demonstrate that most O3 arises from the fumigation of high atmospheric layers, whereas UFPs are generated inside the PBL. O3 contributions from the fumigation of the vertical recirculation of regional air masses, hemispheric transport, and horizontally from direct urban plume transport are shown. Complexity arises from the need to quantify them to abate surface O3.
Alfonso J. Fernández, Michaël Sicard, Maria J. Costa, Juan L. Guerrero-Rascado, José L. Gómez-Amo, Francisco Molero, Rubén Barragán, Daniele Bortoli, Andrés E. Bedoya-Velásquez, María P. Utrillas, Pedro Salvador, María J. Granados-Muñoz, Miguel Potes, Pablo Ortiz-Amezcua, José A. Martínez-Lozano, Begoña Artíñano, Constantino Muñoz-Porcar, Rui Salgado, Roberto Román, Francesc Rocadenbosch, Vanda Salgueiro, José A. Benavent-Oltra, Alejandro Rodríguez-Gómez, Lucas Alados-Arboledas, Adolfo Comerón, and Manuel Pujadas
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2018-370, https://doi.org/10.5194/acp-2018-370, 2018
Revised manuscript not accepted
Guilherme Martins Pereira, Kimmo Teinilä, Danilo Custódio, Aldenor Gomes Santos, Huang Xian, Risto Hillamo, Célia A. Alves, Jailson Bittencourt de Andrade, Gisele Olímpio da Rocha, Prashant Kumar, Rajasekhar Balasubramanian, Maria de Fátima Andrade, and Pérola de Castro Vasconcellos
Atmos. Chem. Phys., 17, 11943–11969, https://doi.org/10.5194/acp-17-11943-2017, https://doi.org/10.5194/acp-17-11943-2017, 2017
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São Paulo, Brazil, has relatively relaxed regulations for ambient air pollution standards and often presents high air pollution levels due to emissions of airborne particles from local sources and long-range transport of biomass burning smoke. High risks associated with particulate matter exposure were observed in most samples. The results highlighted the contribution of vehicular emissions and the significant input from biomass combustion in the dry season.
Evangelia Diapouli, Manousos I. Manousakas, Stergios Vratolis, Vasiliki Vasilatou, Stella Pateraki, Kyriaki A. Bairachtari, Xavier Querol, Fulvio Amato, Andrés Alastuey, Angeliki A. Karanasiou, Franco Lucarelli, Silvia Nava, Giulia Calzolai, Vorne L. Gianelle, Cristina Colombi, Célia Alves, Danilo Custódio, Casimiro Pio, Christos Spyrou, George B. Kallos, and Konstantinos Eleftheriadis
Atmos. Chem. Phys., 17, 3673–3685, https://doi.org/10.5194/acp-17-3673-2017, https://doi.org/10.5194/acp-17-3673-2017, 2017
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This study examined the contribution of two natural sources (long-range transport of African dust and sea salt) to the airborne particulate matter concentrations, in 5 southern European cities (Porto, Barcelona, Milan, Florence, Athens). The results demonstrated that natural sources are often expressed with high-intensity events, leading even to exceedances of the EU air quality standards. This effect was more pronounced in the case of African dust intrusions in the eastern Mediterranean area.
Fulvio Amato, Andrés Alastuey, Angeliki Karanasiou, Franco Lucarelli, Silvia Nava, Giulia Calzolai, Mirko Severi, Silvia Becagli, Vorne L. Gianelle, Cristina Colombi, Celia Alves, Danilo Custódio, Teresa Nunes, Mario Cerqueira, Casimiro Pio, Konstantinos Eleftheriadis, Evangelia Diapouli, Cristina Reche, María Cruz Minguillón, Manousos-Ioannis Manousakas, Thomas Maggos, Stergios Vratolis, Roy M. Harrison, and Xavier Querol
Atmos. Chem. Phys., 16, 3289–3309, https://doi.org/10.5194/acp-16-3289-2016, https://doi.org/10.5194/acp-16-3289-2016, 2016
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Harmonized source apportionment of atmospheric particulate matter (PM10 and PM2.5) at 5 EU cities (Barcelona, Florence, Milan, Athens and Porto) reveals that vehicle exhaust (excluding nitrate) plus non-exhaust contributes 16–32 % to PM10 and 15–36 % to PM2.5. Secondary PM represents 37–82 % of PM2.5. Biomass burning varies from < 2 to 24 % of PM10, depending on the residential heating fuel. Other sources are local dust (7–19 % of PM10), industries (4–11 % of PM10), shipping, sea salt and Saharan dust.
V. Crenn, J. Sciare, P. L. Croteau, S. Verlhac, R. Fröhlich, C. A. Belis, W. Aas, M. Äijälä, A. Alastuey, B. Artiñano, D. Baisnée, N. Bonnaire, M. Bressi, M. Canagaratna, F. Canonaco, C. Carbone, F. Cavalli, E. Coz, M. J. Cubison, J. K. Esser-Gietl, D. C. Green, V. Gros, L. Heikkinen, H. Herrmann, C. Lunder, M. C. Minguillón, G. Močnik, C. D. O'Dowd, J. Ovadnevaite, J.-E. Petit, E. Petralia, L. Poulain, M. Priestman, V. Riffault, A. Ripoll, R. Sarda-Estève, J. G. Slowik, A. Setyan, A. Wiedensohler, U. Baltensperger, A. S. H. Prévôt, J. T. Jayne, and O. Favez
Atmos. Meas. Tech., 8, 5063–5087, https://doi.org/10.5194/amt-8-5063-2015, https://doi.org/10.5194/amt-8-5063-2015, 2015
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A large intercomparison study of 13 Q-ACSM was conducted for a 3-week period in the region of Paris to evaluate the performance of this instrument and to monitor the major NR-PM1 chemical components. Reproducibility expanded uncertainties of Q-ACSM concentration measurements were found to be 9, 15, 19, 28, and 36% for NR-PM1, NO3, OM, SO4, and NH4, respectively. Some recommendations regarding best calibration practices, standardized data processing and data treatment are also provided.
E. Alonso-Blanco, F. J. Gómez-Moreno, L. Núñez, M. Pujadas, M. Cusack, and B. Artíñano
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acpd-15-25231-2015, https://doi.org/10.5194/acpd-15-25231-2015, 2015
Revised manuscript not accepted
R. Fröhlich, V. Crenn, A. Setyan, C. A. Belis, F. Canonaco, O. Favez, V. Riffault, J. G. Slowik, W. Aas, M. Aijälä, A. Alastuey, B. Artiñano, N. Bonnaire, C. Bozzetti, M. Bressi, C. Carbone, E. Coz, P. L. Croteau, M. J. Cubison, J. K. Esser-Gietl, D. C. Green, V. Gros, L. Heikkinen, H. Herrmann, J. T. Jayne, C. R. Lunder, M. C. Minguillón, G. Močnik, C. D. O'Dowd, J. Ovadnevaite, E. Petralia, L. Poulain, M. Priestman, A. Ripoll, R. Sarda-Estève, A. Wiedensohler, U. Baltensperger, J. Sciare, and A. S. H. Prévôt
Atmos. Meas. Tech., 8, 2555–2576, https://doi.org/10.5194/amt-8-2555-2015, https://doi.org/10.5194/amt-8-2555-2015, 2015
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Source apportionment (SA) of organic aerosol mass spectrometric data measured with the Aerodyne ACSM using PMF/ME2 is a frequently used technique in the AMS/ACSM community. ME2 uncertainties due to instrument-to-instrument variations are elucidated by performing SA on ambient data from 14 individual, co-located ACSMs, recorded during the first ACTRIS ACSM intercomparison study at SIRTA near Paris (France). The mean uncertainty was 17.2%. Recommendations for future studies using ME2 are provided.
M. Brines, M. Dall'Osto, D. C. S. Beddows, R. M. Harrison, F. Gómez-Moreno, L. Núñez, B. Artíñano, F. Costabile, G. P. Gobbi, F. Salimi, L. Morawska, C. Sioutas, and X. Querol
Atmos. Chem. Phys., 15, 5929–5945, https://doi.org/10.5194/acp-15-5929-2015, https://doi.org/10.5194/acp-15-5929-2015, 2015
K. E. Yttri, J. Schnelle-Kreis, W. Maenhaut, G. Abbaszade, C. Alves, A. Bjerke, N. Bonnier, R. Bossi, M. Claeys, C. Dye, M. Evtyugina, D. García-Gacio, R. Hillamo, A. Hoffer, M. Hyder, Y. Iinuma, J.-L. Jaffrezo, A. Kasper-Giebl, G. Kiss, P. L. López-Mahia, C. Pio, C. Piot, C. Ramirez-Santa-Cruz, J. Sciare, K. Teinilä, R. Vermeylen, A. Vicente, and R. Zimmermann
Atmos. Meas. Tech., 8, 125–147, https://doi.org/10.5194/amt-8-125-2015, https://doi.org/10.5194/amt-8-125-2015, 2015
J. Fröhlich-Nowoisky, C. Ruzene Nespoli, D. A. Pickersgill, P. E. Galand, I. Müller-Germann, T. Nunes, J. Gomes Cardoso, S. M. Almeida, C. Pio, M. O. Andreae, R. Conrad, U. Pöschl, and V. R. Després
Biogeosciences, 11, 6067–6079, https://doi.org/10.5194/bg-11-6067-2014, https://doi.org/10.5194/bg-11-6067-2014, 2014
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We have investigated the presence of archaea as well as their amoA gene diversity in aerosol particles collected over 1 year in central Europe and found that, within the 16S and amoA gene, Thaumarchaeota prevail and experience a diversity peak in fall, while only few Euryarchaeota were detected primarily in spring. We also compared the results with airborne archaea from Cape Verde and observe that the proportions of Euryarchaeota seem to be enhanced in coastal air compared to continental air.
P. Salvador, S. Alonso-Pérez, J. Pey, B. Artíñano, J. J. de Bustos, A. Alastuey, and X. Querol
Atmos. Chem. Phys., 14, 6759–6775, https://doi.org/10.5194/acp-14-6759-2014, https://doi.org/10.5194/acp-14-6759-2014, 2014
M. Dall'Osto, X. Querol, A. Alastuey, M. C. Minguillon, M. Alier, F. Amato, M. Brines, M. Cusack, J. O. Grimalt, A. Karanasiou, T. Moreno, M. Pandolfi, J. Pey, C. Reche, A. Ripoll, R. Tauler, B. L. Van Drooge, M. Viana, R. M. Harrison, J. Gietl, D. Beddows, W. Bloss, C. O'Dowd, D. Ceburnis, G. Martucci, N. L. Ng, D. Worsnop, J. Wenger, E. Mc Gillicuddy, J. Sodeau, R. Healy, F. Lucarelli, S. Nava, J. L. Jimenez, F. Gomez Moreno, B. Artinano, A. S. H. Prévôt, L. Pfaffenberger, S. Frey, F. Wilsenack, D. Casabona, P. Jiménez-Guerrero, D. Gross, and N. Cots
Atmos. Chem. Phys., 13, 8991–9019, https://doi.org/10.5194/acp-13-8991-2013, https://doi.org/10.5194/acp-13-8991-2013, 2013
X. Querol, A. Alastuey, M. Viana, T. Moreno, C. Reche, M. C. Minguillón, A. Ripoll, M. Pandolfi, F. Amato, A. Karanasiou, N. Pérez, J. Pey, M. Cusack, R. Vázquez, F. Plana, M. Dall'Osto, J. de la Rosa, A. Sánchez de la Campa, R. Fernández-Camacho, S. Rodríguez, C. Pio, L. Alados-Arboledas, G. Titos, B. Artíñano, P. Salvador, S. García Dos Santos, and R. Fernández Patier
Atmos. Chem. Phys., 13, 6185–6206, https://doi.org/10.5194/acp-13-6185-2013, https://doi.org/10.5194/acp-13-6185-2013, 2013
Related subject area
Subject: Aerosols | Research Activity: Field Measurements | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
A multi-site passive approach to studying the emissions and evolution of smoke from prescribed fires
The annual cycle and sources of relevant aerosol precursor vapors in the central Arctic during the MOSAiC expedition
Opinion: How will advances in aerosol science inform our understanding of the health impacts of outdoor particulate pollution?
Measurement report: Intra-annual variability of black carbon and brown carbon and their interrelation with meteorological conditions over Gangtok, Sikkim
Long-range transport of air pollutants increases the concentration of hazardous components of PM2.5 in northern South America
Dominant influence of biomass combustion and cross-border transport on nitrogen-containing organic compound levels in the southeastern Tibetan Plateau
Impacts of elevated anthropogenic emissions on physicochemical characteristics of black-carbon-containing particles over the Tibetan Plateau
Online characterization of primary and secondary emissions of particulate matter and acidic molecules from a modern fleet of city buses
Atmospheric evolution of environmentally persistent free radicals in the rural North China Plain: effects on water solubility and PM2.5 oxidative potential
Two distinct ship emission profiles for organic-sulfate source apportionment of PM in sulfur emission control areas
Automated compound speciation, cluster analysis, and quantification of organic vapors and aerosols using comprehensive two-dimensional gas chromatography and mass spectrometry
Measurement report: Occurrence of aminiums in PM2.5 during winter in China – aminium outbreak during polluted episodes and potential constraints
Bridging gas and aerosol properties between the northeastern US and Bermuda: analysis of eight transit flights
The behaviour of charged particles (ions) during new particle formation events in urban Leipzig, Germany
Exploring the sources of light-absorbing carbonaceous aerosols by integrating observational and modeling results: insights from Northeast China
Measurement report: Characteristics of airborne black-carbon-containing particles during the 2021 summer COVID-19 lockdown in a typical Yangtze River Delta city, China
Aerosol optical properties within the atmospheric boundary layer predicted from ground-based observations compared to Raman lidar retrievals during RITA-2021
Hygroscopic growth and activation changed submicron aerosol composition and properties in the North China Plain
Measurement report: Formation of tropospheric brown carbon in a lifting air mass
Vertical variability of aerosol properties and trace gases over a remote marine region: a case study over Bermuda
Differences in aerosol and cloud properties along the central California coast when winds change from northerly to southerly
International airport emissions and their impact on local air quality: chemical speciation of ambient aerosols at Madrid–Barajas Airport during the AVIATOR campaign
Significant role of biomass burning in heavy haze formation in a megacity: Molecular-level insights from intensive PM2.5 sampling on winter hazy days
The local ship speed reduction effect on black carbon emissions measured at a remote marine station
High-altitude aerosol chemical characterization and source identification: insights from the CALISHTO campaign
Measurement report: Impact of emission control measures on environmental persistent free radicals and reactive oxygen species – a short-term case study in Beijing
Characterizing water solubility of fresh and aged secondary organic aerosol in PM2.5 with the stable carbon isotope technique
Measurement report: Impact of cloud processes on secondary organic aerosols at a forested mountain site in southeastern China
Critical contribution of chemically diverse carbonyl molecules to the oxidative potential of atmospheric aerosols
Seasonal Investigation of Ultrafine Particle Composition in an Eastern Amazonian Rainforest
Measurement report: Vanadium-containing ship exhaust particles detected in and above the marine boundary layer in the remote atmosphere
Diverging trends in aerosol sulfate and nitrate measured in the remote North Atlantic in Barbados are attributed to clean air policies, African smoke, and anthropogenic emissions
Technical note: Quantified organic aerosol subsaturated hygroscopicity by a simple optical scatter monitor system through field measurements
Diverse sources and aging change the mixing state and ice nucleation properties of aerosol particles over the western Pacific and Southern Ocean
The water-insoluble organic carbon in PM2.5 of typical Chinese urban areas: light-absorbing properties, potential sources, radiative forcing effects, and a possible light-absorbing continuum
Measurement report: Size-resolved secondary organic aerosol formation modulated by aerosol water uptake in wintertime haze
In situ measurement of organic aerosol molecular markers in urban Hong Kong during a summer period: temporal variations and source apportionment
Technical note: Determining chemical composition of atmospheric single particles by a standard-free mass calibration algorithm
Different formation pathways of nitrogen-containing organic compounds in aerosols and fog water in northern China
Impact of weather patterns and meteorological factors on PM2.5 and O3 responses to the COVID-19 lockdown in China
Daytime and nighttime aerosol soluble iron formation in clean and slightly polluted moist air in a coastal city in eastern China
Non-negligible secondary contribution to brown carbon in autumn and winter: inspiration from particulate nitrated and oxygenated aromatic compounds in urban Beijing
Non-sea-salt aerosols that contain trace bromine and iodine are widespread in the remote troposphere
Simultaneous organic aerosol source apportionment at two Antarctic sites reveals large-scale and ecoregion-specific components
Measurement report: Optical characterization, seasonality, and sources of brown carbon in fine aerosols from Tianjin, North China: year-round observations
High-resolution analyses of concentrations and sizes of black carbon particles deposited on northwest Greenland over the past 350 years – Part 2: Seasonal and temporal trends in black carbon originated from fossil fuel combustion and biomass burning
Bayesian inference-based estimation of hourly primary and secondary organic carbon in suburban Hong Kong: multi-temporal-scale variations and evolution characteristics during PM2.5 episodes
Formation and chemical evolution of SOA in two different environments: A dual chamber study
Enhanced daytime secondary aerosol formation driven by gas-particle partitioning in downwind urban plumes
Multiple eco-regions contribute to the seasonal cycle of Antarctic aerosol size distributions
Rime El Asmar, Zongrun Li, David J. Tanner, Yongtao Hu, Susan O'Neill, L. Gregory Huey, M. Talat Odman, and Rodney J. Weber
Atmos. Chem. Phys., 24, 12749–12773, https://doi.org/10.5194/acp-24-12749-2024, https://doi.org/10.5194/acp-24-12749-2024, 2024
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Prescribed burning is an important method for managing ecosystems and preventing wildfires. However, smoke from prescribed fires can have a significant impact on air quality. Here, using a network of fixed sites and sampling throughout an extended prescribed burning period in 2 different years, we characterize emissions and evolutions of up to 8 h of PM2.5 mass, black carbon (BC), and brown carbon (BrC) in smoke from burning of forested lands in the southeastern USA.
Matthew Boyer, Diego Aliaga, Lauriane L. J. Quéléver, Silvia Bucci, Hélène Angot, Lubna Dada, Benjamin Heutte, Lisa Beck, Marina Duetsch, Andreas Stohl, Ivo Beck, Tiia Laurila, Nina Sarnela, Roseline C. Thakur, Branka Miljevic, Markku Kulmala, Tuukka Petäjä, Mikko Sipilä, Julia Schmale, and Tuija Jokinen
Atmos. Chem. Phys., 24, 12595–12621, https://doi.org/10.5194/acp-24-12595-2024, https://doi.org/10.5194/acp-24-12595-2024, 2024
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We analyze the seasonal cycle and sources of gases that are relevant for the formation of aerosol particles in the central Arctic. Since theses gases can form new particles, they can influence Arctic climate. We show that the sources of these gases are associated with changes in the Arctic environment during the year, especially with respect to sea ice. Therefore, the concentration of these gases will likely change in the future as the Arctic continues to warm.
Imad El Haddad, Danielle Vienneau, Kaspar R. Daellenbach, Robin Modini, Jay G. Slowik, Abhishek Upadhyay, Petros N. Vasilakos, David Bell, Kees de Hoogh, and Andre S. H. Prevot
Atmos. Chem. Phys., 24, 11981–12011, https://doi.org/10.5194/acp-24-11981-2024, https://doi.org/10.5194/acp-24-11981-2024, 2024
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This opinion paper explores how advances in aerosol science inform our understanding of the health impacts of outdoor particulate pollution. We advocate for a shift in the way we target PM pollution, focusing on the most harmful anthropogenic emissions. We highlight key observations, modelling developments, and emission measurements needed to achieve this shift.
Pramod Kumar, Khushboo Sharma, Ankita Malu, Rajeev Rajak, Aparna Gupta, Bidyutjyoti Baruah, Shailesh Yadav, Thupstan Angchuk, Jayant Sharma, Rakesh Kumar Ranjan, Anil Kumar Misra, and Nishchal Wanjari
Atmos. Chem. Phys., 24, 11585–11601, https://doi.org/10.5194/acp-24-11585-2024, https://doi.org/10.5194/acp-24-11585-2024, 2024
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This work monitors and assesses air pollution, especially black and brown carbon, its controlling factor, and its effect on the environment of Sikkim Himalayan region. The huge urban sprawl in recent decades has led to regional human-induced air pollution in the region. Black carbon was highest in April 2021 and March 2022, exceeding the WHO limit. The monsoon season causes huge rainfall over the region, which reduces the pollutants by scavenging (rainout and washout).
Maria P. Velásquez-García, K. Santiago Hernández, James A. Vergara-Correa, Richard J. Pope, Miriam Gómez-Marín, and Angela M. Rendón
Atmos. Chem. Phys., 24, 11497–11520, https://doi.org/10.5194/acp-24-11497-2024, https://doi.org/10.5194/acp-24-11497-2024, 2024
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In the Aburrá Valley, northern South America, local emissions determine air quality conditions. However, we found that external sources, such as regional fires, Saharan dust, and volcanic emissions, increase particulate concentrations and worsen chemical composition by introducing elements like heavy metals. Dry winds and source variability contribute to seasonal influences on these events. This study assesses the air quality risks posed by such events, which can affect broad regions worldwide.
Meng Wang, Qiyuan Wang, Steven Sai Hang Ho, Jie Tian, Yong Zhang, Shun-cheng Lee, and Junji Cao
Atmos. Chem. Phys., 24, 11175–11189, https://doi.org/10.5194/acp-24-11175-2024, https://doi.org/10.5194/acp-24-11175-2024, 2024
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We studied nitrogen-containing organic compounds (NOCs) in particulate matter <2.5 µm particles on the southeastern Tibetan Plateau. We found that biomass burning and transboundary transport are the main sources of NOCs in the high-altitude area. Understanding these aerosol sources informs how they add to regional and potentially global climate changes. Our findings could help shape effective environmental policies to enhance air quality and address climate impacts in this sensitive region.
Jinbo Wang, Jiaping Wang, Yuxuan Zhang, Tengyu Liu, Xuguang Chi, Xin Huang, Dafeng Ge, Shiyi Lai, Caijun Zhu, Lei Wang, Qiaozhi Zha, Ximeng Qi, Wei Nie, Congbin Fu, and Aijun Ding
Atmos. Chem. Phys., 24, 11063–11080, https://doi.org/10.5194/acp-24-11063-2024, https://doi.org/10.5194/acp-24-11063-2024, 2024
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In this study, we found large spatial discrepancies in the physical and chemical properties of black carbon over the Tibetan Plateau (TP). Elevated anthropogenic emissions from low-altitude regions can significantly change the mass concentration, mixing state and chemical composition of black-carbon-containing aerosol in the TP region, further altering its light absorption ability. Our study emphasizes the vulnerability of remote plateau regions to intense anthropogenic influences.
Liyuan Zhou, Qianyun Liu, Christian M. Salvador, Michael Le Breton, Mattias Hallquist, Jian Zhen Yu, Chak K. Chan, and Åsa M. Hallquist
Atmos. Chem. Phys., 24, 11045–11061, https://doi.org/10.5194/acp-24-11045-2024, https://doi.org/10.5194/acp-24-11045-2024, 2024
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Our research on city bus emissions reveals that alternative fuels (compressed natural gas and biofuels) reduce fresh particle emissions compared to diesel. However, all fuels lead to secondary air pollution. Aiming at guiding better environmental policies, we studied 76 buses using advanced emission measurement techniques. This work sheds light on the complex effects of bus fuels on urban air quality, emphasizing the need for comprehensive evaluations of future transportation technologies.
Xu Yang, Fobang Liu, Shuqi Yang, Yuling Yang, Yanan Wang, Jingjing Li, Mingyu Zhao, Zhao Wang, Kai Wang, Chi He, and Haijie Tong
Atmos. Chem. Phys., 24, 11029–11043, https://doi.org/10.5194/acp-24-11029-2024, https://doi.org/10.5194/acp-24-11029-2024, 2024
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A study in the rural North China Plain showed environmentally persistent free radicals (EPFRs) in atmospheric particulate matter (PM), with a notable water-soluble fraction likely from atmospheric oxidation during transport. Significant positive correlations between EPFRs and the water-soluble oxidative potential of PM2.5 were found, primarily attributable to the water-soluble fractions of EPFRs. These findings emphasize understanding EPFRs' atmospheric evolution for climate and health impacts.
Kirsten N. Fossum, Chunshui Lin, Niall O'Sullivan, Lu Lei, Stig Hellebust, Darius Ceburnis, Aqeel Afzal, Anja Tremper, David Green, Srishti Jain, Steigvilė Byčenkienė, Colin O'Dowd, John Wenger, and Jurgita Ovadnevaite
Atmos. Chem. Phys., 24, 10815–10831, https://doi.org/10.5194/acp-24-10815-2024, https://doi.org/10.5194/acp-24-10815-2024, 2024
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The chemical composition and sources of submicron aerosol in the Dublin Port area were investigated over a month-long campaign. Two distinct types of ship emissions were identified and characterised: sulfate-rich plumes from the use of heavy fuel oil with scrubbers and organic-rich plumes from the use of low-sulfur fuels. The latter were more frequent, emitting double the particle number and having a typical V / Ni ratio for ship emission.
Xiao He, Xuan Zheng, Shuwen Guo, Lewei Zeng, Ting Chen, Bohan Yang, Shupei Xiao, Qiongqiong Wang, Zhiyuan Li, Yan You, Shaojun Zhang, and Ye Wu
Atmos. Chem. Phys., 24, 10655–10666, https://doi.org/10.5194/acp-24-10655-2024, https://doi.org/10.5194/acp-24-10655-2024, 2024
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This study introduces an innovative method for identifying and quantifying complex organic vapors and aerosols. By combining advanced analytical techniques and new algorithms, we categorized thousands of compounds from heavy-duty diesel vehicles and ambient air and highlighted specific tracers for emission sources. The innovative approach enhances peak identification, reduces quantification uncertainties, and offers new insights for air quality management and atmospheric chemistry.
Yu Xu, Tang Liu, Yi-Jia Ma, Qi-Bin Sun, Hong-Wei Xiao, Hao Xiao, Hua-Yun Xiao, and Cong-Qiang Liu
Atmos. Chem. Phys., 24, 10531–10542, https://doi.org/10.5194/acp-24-10531-2024, https://doi.org/10.5194/acp-24-10531-2024, 2024
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This study investigates the characteristics of aminiums and ammonium in PM2.5 on clean and polluted winter days in 11 Chinese cities, highlighting the possibility of the competitive uptake of ammonia versus amines on acidic aerosols or the displacement of aminiums by ammonia under high-ammonia conditions. The overall results deepen the understanding of the spatiotemporal differences in aminium characteristics and formation in China.
Cassidy Soloff, Taiwo Ajayi, Yonghoon Choi, Ewan C. Crosbie, Joshua P. DiGangi, Glenn S. Diskin, Marta A. Fenn, Richard A. Ferrare, Francesca Gallo, Johnathan W. Hair, Miguel Ricardo A. Hilario, Simon Kirschler, Richard H. Moore, Taylor J. Shingler, Michael A. Shook, Kenneth L. Thornhill, Christiane Voigt, Edward L. Winstead, Luke D. Ziemba, and Armin Sorooshian
Atmos. Chem. Phys., 24, 10385–10408, https://doi.org/10.5194/acp-24-10385-2024, https://doi.org/10.5194/acp-24-10385-2024, 2024
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Using aircraft measurements over the northwestern Atlantic between the US East Coast and Bermuda and trajectory modeling of continental outflow, we identify trace gas and particle properties that exhibit gradients with offshore distance and quantify these changes with high-resolution measurements of concentrations and particle chemistry, size, and scattering properties. This work furthers our understanding of the complex interactions between continental and marine environments.
Alex Rowell, James Brean, David C. S. Beddows, Zongbo Shi, Avinash Kumar, Matti Rissanen, Miikka Dal Maso, Peter Mettke, Kay Weinhold, Maik Merkel, and Roy M. Harrison
Atmos. Chem. Phys., 24, 10349–10361, https://doi.org/10.5194/acp-24-10349-2024, https://doi.org/10.5194/acp-24-10349-2024, 2024
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Ions enhance the formation and growth rates of new particles, affecting the Earth's radiation budget. Despite these effects, there is little published data exploring the sources of ions in the urban environment and their role in new particle formation (NPF). Here we show that natural ion sources dominate in urban environments, while traffic is a secondary source. Ions contribute up to 12.7 % of the formation rate of particles, indicating that they are important for forming urban PM.
Yuan Cheng, Xu-bing Cao, Sheng-qiang Zhu, Zhi-qing Zhang, Jiu-meng Liu, Hong-liang Zhang, Qiang Zhang, and Ke-bin He
Atmos. Chem. Phys., 24, 9869–9883, https://doi.org/10.5194/acp-24-9869-2024, https://doi.org/10.5194/acp-24-9869-2024, 2024
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The agreement between observational and modeling results is essential for the development of efficient air pollution control strategies. Here we constrained the modeling results of carbonaceous aerosols by field observation in Northeast China, a historically overlooked but recently targeted region of national clean-air actions. Our study suggested that the simulation of agricultural fire emissions and secondary organic aerosols remains challenging.
Yuan Dai, Junfeng Wang, Houjun Wang, Shijie Cui, Yunjiang Zhang, Haiwei Li, Yun Wu, Ming Wang, Eleonora Aruffo, and Xinlei Ge
Atmos. Chem. Phys., 24, 9733–9748, https://doi.org/10.5194/acp-24-9733-2024, https://doi.org/10.5194/acp-24-9733-2024, 2024
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Short-term strict emission control can improve air quality, but its effectiveness needs assessment. During the 2021 summer COVID-19 lockdown in Yangzhou, we found that PM2.5 levels did not decrease despite reduced primary emissions. Aged black-carbon particles increased substantially due to higher O3 levels and transported pollutants. High humidity and low wind also played key roles. The results highlight the importance of a regionally balanced control strategy for future air quality management.
Xinya Liu, Diego Alves Gouveia, Bas Henzing, Arnoud Apituley, Arjan Hensen, Danielle van Dinther, Rujin Huang, and Ulrike Dusek
Atmos. Chem. Phys., 24, 9597–9614, https://doi.org/10.5194/acp-24-9597-2024, https://doi.org/10.5194/acp-24-9597-2024, 2024
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The vertical distribution of aerosol optical properties is important for their effect on climate. This is usually measured by lidar, which has limitations, most notably the assumption of a lidar ratio. Our study shows that routine surface-level aerosol measurements are able to predict this lidar ratio reasonably well within the lower layers of the atmosphere and thus provide a relatively simple and cost-effective method to improve lidar measurements.
Weiqi Xu, Ye Kuang, Wanyun Xu, Zhiqiang Zhang, Biao Luo, Xiaoyi Zhang, Jiangchuang Tao, Hongqin Qiao, Li Liu, and Yele Sun
Atmos. Chem. Phys., 24, 9387–9399, https://doi.org/10.5194/acp-24-9387-2024, https://doi.org/10.5194/acp-24-9387-2024, 2024
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We deployed an advanced aerosol–fog sampling system at a rural site in the North China Plain to investigate impacts of aerosol hygroscopic growth and activation on the physicochemical properties of submicron aerosols. Observed results highlighted remarkably different aqueous processing of primary and secondary submicron aerosol components under distinct ambient relative humidity (RH) conditions and that RH levels significantly impact aerosol sampling through the aerosol swelling effect.
Can Wu, Xiaodi Liu, Ke Zhang, Si Zhang, Cong Cao, Jianjun Li, Rui Li, Fan Zhang, and Gehui Wang
Atmos. Chem. Phys., 24, 9263–9275, https://doi.org/10.5194/acp-24-9263-2024, https://doi.org/10.5194/acp-24-9263-2024, 2024
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Brown carbon (BrC) is prevalent in the troposphere and can efficiently absorb solar and terrestrial radiation. Our observations show that the enhanced light absorption of BrC relative to black carbon at the tropopause can be attributed to the formation of nitrogen-containing organic compounds through the aqueous-phase reactions of carbonyls with ammonium.
Taiwo Ajayi, Yonghoon Choi, Ewan C. Crosbie, Joshua P. DiGangi, Glenn S. Diskin, Marta A. Fenn, Richard A. Ferrare, Johnathan W. Hair, Miguel Ricardo A. Hilario, Chris A. Hostetler, Simon Kirschler, Richard H. Moore, Taylor J. Shingler, Michael A. Shook, Cassidy Soloff, Kenneth L. Thornhill, Christiane Voigt, Edward L. Winstead, Luke D. Ziemba, and Armin Sorooshian
Atmos. Chem. Phys., 24, 9197–9218, https://doi.org/10.5194/acp-24-9197-2024, https://doi.org/10.5194/acp-24-9197-2024, 2024
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This study uses airborne data to examine vertical profiles of trace gases, aerosol particles, and meteorological variables over a remote marine area (Bermuda). Results show distinct differences based on both air mass source region (North America, Ocean, Caribbean/North Africa) and altitude for a given air mass type. This work highlights the sensitivity of remote marine areas to long-range transport and the importance of considering the vertical dependence of trace gas and aerosol properties.
Kira Zeider, Grace Betito, Anthony Bucholtz, Peng Xian, Annette Walker, and Armin Sorooshian
Atmos. Chem. Phys., 24, 9059–9083, https://doi.org/10.5194/acp-24-9059-2024, https://doi.org/10.5194/acp-24-9059-2024, 2024
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The predominant wind direction along the California coast (northerly) reverses several times during the summer (to southerly). The effects of these wind reversals on aerosol and cloud characteristics are not well understood. Using data from multiple datasets we found that southerly flow periods had enhanced signatures of anthropogenic emissions due to shipping and continental sources, and clouds had more but smaller droplets.
Saleh Alzahrani, Doğuşhan Kılıç, Michael Flynn, Paul I. Williams, and James Allan
Atmos. Chem. Phys., 24, 9045–9058, https://doi.org/10.5194/acp-24-9045-2024, https://doi.org/10.5194/acp-24-9045-2024, 2024
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This paper investigates emissions from aviation activities at an international airport to evaluate their impact on local air quality. The study provides detailed insights into the chemical composition of aerosols and key pollutants in the airport environment. Source apportionment analysis using positive matrix factorisation (PMF) identified three significant sources: less oxidised oxygenated organic aerosol, alkane organic aerosol, and more oxidised oxygenated organic aerosol.
Mingjie Kang, Mengying Bao, Wenhuai Song, Aduburexiati Abulimiti, Fang Cao, Sönke Szidat, and Yanlin Zhang
EGUsphere, https://doi.org/10.5194/egusphere-2024-2098, https://doi.org/10.5194/egusphere-2024-2098, 2024
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Reports on the molecular level knowledge of high temporal resolution PM2.5 components on hazy days are still limited. This study investigated many individual PM2.5 species and sources. The results show biomass burning (BB) was the main source of organic carbon. Moreover, BB enhanced fungal spore emissions and secondary aerosol formation. The contribution of non-fossils increased with increasing haze pollution. These findings suggest BB may be an important driver of haze events in winter.
Mikko Heikkilä, Krista Luoma, Timo Mäkelä, and Tiia Grönholm
Atmos. Chem. Phys., 24, 8927–8941, https://doi.org/10.5194/acp-24-8927-2024, https://doi.org/10.5194/acp-24-8927-2024, 2024
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Black carbon (BC) concentration was measured from 211 ship exhaust gas plumes at a remote marine station. Emission factors of BC were calculated in grams per kilogram of fuel. Ships with an exhaust gas cleaning system (EGCS) were found to have median BC emissions per fuel consumed 5 times lower than ships without an EGCS. However, this might be because of non-EGCS ships running at low engine loads rather than the EGCS itself. A local speed restriction would increase BC emissions of ships.
Olga Zografou, Maria Gini, Prodromos Fetfatzis, Konstantinos Granakis, Romanos Foskinis, Manousos Ioannis Manousakas, Fotios Tsopelas, Evangelia Diapouli, Eleni Dovrou, Christina N. Vasilakopoulou, Alexandros Papayannis, Spyros N. Pandis, Athanasios Nenes, and Konstantinos Eleftheriadis
Atmos. Chem. Phys., 24, 8911–8926, https://doi.org/10.5194/acp-24-8911-2024, https://doi.org/10.5194/acp-24-8911-2024, 2024
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Characterization of PM1 and positive matrix factorization (PMF) source apportionment of organic and inorganic fractions were conducted at the high-altitude station (HAC)2. Cloud presence reduced PM1, affecting sulfate more than organics. Free-troposphere (FT) conditions showed more black carbon (eBC) than planetary boundary layer (PBL) conditions.
Yuanyuan Qin, Xinghua Zhang, Wei Huang, Juanjuan Qin, Xiaoyu Hu, Yuxuan Cao, Tianyi Zhao, Yang Zhang, Jihua Tan, Ziyin Zhang, Xinming Wang, and Zhenzhen Wang
Atmos. Chem. Phys., 24, 8737–8750, https://doi.org/10.5194/acp-24-8737-2024, https://doi.org/10.5194/acp-24-8737-2024, 2024
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Environmental persistent free radicals (EPFRs) and reactive oxygen species (ROSs) play an active role in the atmosphere. Despite control measures having effectively reduced their emissions, reductions were less than in PM2.5. Emission control measures performed well in achieving Parade Blue, but reducing the impact of the atmosphere on human health remains challenging. Thus, there is a need to reassess emission control measures to better address the challenges posed by EPFRs and ROSs.
Fenghua Wei, Xing Peng, Liming Cao, Mengxue Tang, Ning Feng, Xiaofeng Huang, and Lingyan He
Atmos. Chem. Phys., 24, 8507–8518, https://doi.org/10.5194/acp-24-8507-2024, https://doi.org/10.5194/acp-24-8507-2024, 2024
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The water solubility of secondary organic aerosols (SOAs) is a crucial factor in determining their hygroscopicity and climatic impact. Stable carbon isotope and mass spectrometry techniques were combined to assess the water solubility of SOAs with different aging degrees in a coastal megacity in China. This work revealed a much higher water-soluble fraction of aged SOA compared to fresh SOA, indicating that the aging degree of SOA has considerable impacts on its water solubility.
Zijun Zhang, Weiqi Xu, Yi Zhang, Wei Zhou, Xiangyu Xu, Aodong Du, Yinzhou Zhang, Hongqin Qiao, Ye Kuang, Xiaole Pan, Zifa Wang, Xueling Cheng, Lanzhong Liu, Qingyan Fu, Douglas R. Worsnop, Jie Li, and Yele Sun
Atmos. Chem. Phys., 24, 8473–8488, https://doi.org/10.5194/acp-24-8473-2024, https://doi.org/10.5194/acp-24-8473-2024, 2024
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We investigated aerosol composition and sources and the interaction between secondary organic aerosol (SOA) and clouds at a regional mountain site in southeastern China. Clouds efficiently scavenge more oxidized SOA; however, cloud evaporation leads to the production of less oxidized SOA. The unexpectedly high presence of nitrate in aerosol particles indicates that nitrate formed in polluted areas has undergone interactions with clouds, significantly influencing the regional background site.
Feifei Li, Shanshan Tang, Jitao Lv, Shiyang Yu, Xu Sun, Dong Cao, Yawei Wang, and Guibin Jiang
Atmos. Chem. Phys., 24, 8397–8411, https://doi.org/10.5194/acp-24-8397-2024, https://doi.org/10.5194/acp-24-8397-2024, 2024
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Targeted derivatization and non-targeted analysis with Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) were used to reveal the molecular composition of carbonyl molecules in PM2.5, and the important role of carbonyls in increasing the oxidative potential of organic aerosol was found in real samples.
Adam E. Thomas, Hayley S. Glicker, Alex B. Guenther, Roger Seco, Oscar Vega Bustillos, Julio Tota, Rodrigo A. F. Souza, and James N. Smith
EGUsphere, https://doi.org/10.5194/egusphere-2024-2230, https://doi.org/10.5194/egusphere-2024-2230, 2024
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We present measurements of the composition of ultrafine particles collected from the eastern Amazon, a relatively understudied region that is subjected to increasing human influence. We find that while isoprene chemistry is likely significant to ultrafine particle growth throughout the year, compounds related to other sources such as biological spore emissions and biomass burning exhibit striking seasonal differences, implying an extensive variation in regional ultrafine particle sources.
Maya Abou-Ghanem, Daniel M. Murphy, Gregory P. Schill, Michael J. Lawler, and Karl D. Froyd
Atmos. Chem. Phys., 24, 8263–8275, https://doi.org/10.5194/acp-24-8263-2024, https://doi.org/10.5194/acp-24-8263-2024, 2024
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Using particle analysis by laser mass spectrometry, we examine vanadium-containing ship exhaust particles measured on NASA's DC-8 during the Atmospheric Tomography Mission (ATom). Our results reveal ship exhaust particles are sufficiently widespread in the marine atmosphere and experience atmospheric aging. Finally, we use laboratory calibrations to determine the vanadium, sulfate, and organic single-particle mass fractions of vanadium-containing ship exhaust particles.
Cassandra J. Gaston, Joseph M. Prospero, Kristen Foley, Havala O. T. Pye, Lillian Custals, Edmund Blades, Peter Sealy, and James A. Christie
Atmos. Chem. Phys., 24, 8049–8066, https://doi.org/10.5194/acp-24-8049-2024, https://doi.org/10.5194/acp-24-8049-2024, 2024
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To understand how changing emissions have impacted aerosols in remote regions, we measured nitrate and sulfate in Barbados and compared them to model predictions from EPA’s Air QUAlity TimE Series (EQUATES). Nitrate was stable, except for spikes in 2008 and 2010 due to transported smoke. Sulfate decreased in the 1990s due to reductions in sulfur dioxide (SO2) in the US and Europe; then it increased in the 2000s, likely due to anthropogenic emissions from Africa.
Jie Zhang, Tianyu Zhu, Alexandra Catena, Yaowei Li, Margaret Schwab, Pengfei Liu, Akua Asa-Awuku, and James Schwab
EGUsphere, https://doi.org/10.5194/egusphere-2024-1390, https://doi.org/10.5194/egusphere-2024-1390, 2024
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This study shows the derived organic aerosol hygroscopicity under high humidity conditions based on a simple optical scatter monitor system, including two nephelometric monitors (pDR-1500), after knowing the aerosol chemical composition.
Jiao Xue, Tian Zhang, Keyhong Park, Jinpei Yan, Young Jun Yoon, Jiyeon Park, and Bingbing Wang
Atmos. Chem. Phys., 24, 7731–7754, https://doi.org/10.5194/acp-24-7731-2024, https://doi.org/10.5194/acp-24-7731-2024, 2024
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Ice formation by particles is an important way of making mixed-phase and ice clouds. We found that particles collected in the marine atmosphere exhibit diverse ice nucleation abilities and mixing states. Sea salt mixed-sulfate particles were enriched in ice-nucleating particles. Selective aging on sea salt particles made particle populations more externally mixed. Characterizations of particles and their mixing state are needed for a better understanding of aerosol–cloud interactions.
Yangzhi Mo, Jun Li, Guangcai Zhong, Sanyuan Zhu, Shizhen Zhao, Jiao Tang, Hongxing Jiang, Zhineng Cheng, Chongguo Tian, Yingjun Chen, and Gan Zhang
Atmos. Chem. Phys., 24, 7755–7772, https://doi.org/10.5194/acp-24-7755-2024, https://doi.org/10.5194/acp-24-7755-2024, 2024
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In this study, we found that biomass burning (31.0 %) and coal combustion (31.1 %) were the dominant sources of water-insoluble organic carbon in China, with coal combustion sources exhibiting the strongest light-absorbing capacity. Additionally, we propose a light-absorbing carbonaceous continuum, revealing that components enriched with fossil sources tend to have stronger light-absorbing capacity, higher aromaticity, higher molecular weights, and greater recalcitrance in the atmosphere.
Jing Duan, Ru-Jin Huang, Ying Wang, Wei Xu, Haobin Zhong, Chunshui Lin, Wei Huang, Yifang Gu, Jurgita Ovadnevaite, Darius Ceburnis, and Colin O'Dowd
Atmos. Chem. Phys., 24, 7687–7698, https://doi.org/10.5194/acp-24-7687-2024, https://doi.org/10.5194/acp-24-7687-2024, 2024
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The chemical composition of atmospheric particles has shown significant changes in recent years. We investigated the potential effects of changes in inorganics on aerosol water uptake and, thus, secondary organic aerosol formation in wintertime haze based on the size-resolved measurements of non-refractory fine particulate matter (NR-PM2.5) in Xi’an, northwestern China. We highlight the key role of aerosol water as a medium to link inorganics and organics in their multiphase processes.
Hongyong Li, Xiaopu Lyu, Likun Xue, Yunxi Huo, Dawen Yao, Haoxian Lu, and Hai Guo
Atmos. Chem. Phys., 24, 7085–7100, https://doi.org/10.5194/acp-24-7085-2024, https://doi.org/10.5194/acp-24-7085-2024, 2024
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Organic aerosol is ubiquitous in the atmosphere and largely explains the gap between current levels of fine particulate matter in many cities and the World Health Organization guideline values. This study highlights the dominant contributions of cooking emissions to organic aerosol when marine air prevailed in Hong Kong, which were occasionally overwhelmed by aromatics-derived secondary organic aerosol in continental ouflows.
Shao Shi, Jinghao Zhai, Xin Yang, Yechun Ruan, Yuanlong Huang, Xujian Chen, Antai Zhang, Jianhuai Ye, Guomao Zheng, Baohua Cai, Yaling Zeng, Yixiang Wang, Chunbo Xing, Yujie Zhang, Tzung-May Fu, Lei Zhu, Huizhong Shen, and Chen Wang
Atmos. Chem. Phys., 24, 7001–7012, https://doi.org/10.5194/acp-24-7001-2024, https://doi.org/10.5194/acp-24-7001-2024, 2024
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The determination of ions in the mass spectra of individual particles remains uncertain. We have developed a standard-free mass calibration algorithm applicable to more than 98 % of ambient particles. With our algorithm, ions with ~ 0.05 Th mass difference could be determined. Therefore, many more atmospheric species could be determined and involved in the source apportionment of aerosols, the study of chemical reaction mechanisms, and the analysis of single-particle mixing states.
Wei Sun, Xiaodong Hu, Yuzhen Fu, Guohua Zhang, Yujiao Zhu, Xinfeng Wang, Caiqing Yan, Likun Xue, He Meng, Bin Jiang, Yuhong Liao, Xinming Wang, Ping'an Peng, and Xinhui Bi
Atmos. Chem. Phys., 24, 6987–6999, https://doi.org/10.5194/acp-24-6987-2024, https://doi.org/10.5194/acp-24-6987-2024, 2024
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The formation pathways of nitrogen-containing compounds (NOCs) in the atmosphere remain unclear. We investigated the composition of aerosols and fog water by state-of-the-art mass spectrometry and compared the formation pathways of NOCs. We found that NOCs in aerosols were mainly formed through nitration reaction, while ammonia addition played a more important role in fog water. The results deepen our understanding of the processes of organic particulate pollution.
Fuzhen Shen, Michaela I. Hegglin, and Yue Yuan
Atmos. Chem. Phys., 24, 6539–6553, https://doi.org/10.5194/acp-24-6539-2024, https://doi.org/10.5194/acp-24-6539-2024, 2024
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We attempt to use a novel structural self-organising map and machine learning models to identify a weather system and quantify the importance of each meteorological factor in driving the unexpected PM2.5 and O3 changes under the specific weather system during the COVID-19 lockdown in China. The result highlights that temperature under the double-centre high-pressure system plays the most crucial role in abnormal events.
Wenshuai Li, Yuxuan Qi, Yingchen Liu, Guanru Wu, Yanjing Zhang, Jinhui Shi, Wenjun Qu, Lifang Sheng, Wencai Wang, Daizhou Zhang, and Yang Zhou
Atmos. Chem. Phys., 24, 6495–6508, https://doi.org/10.5194/acp-24-6495-2024, https://doi.org/10.5194/acp-24-6495-2024, 2024
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Aerosol particles from mainland can transport to oceans and deposit, providing soluble Fe and affecting phytoplankton growth. Thus, we studied the dissolution process of aerosol Fe and found that photochemistry played a key role in promoting Fe dissolution in clean conditions. RH-dependent reactions were more influential in slightly polluted conditions. These results highlight the distinct roles of two weather-related parameters (radiation and RH) in influencing geochemical cycles related to Fe.
Yanqin Ren, Zhenhai Wu, Yuanyuan Ji, Fang Bi, Junling Li, Haijie Zhang, Hao Zhang, Hong Li, and Gehui Wang
Atmos. Chem. Phys., 24, 6525–6538, https://doi.org/10.5194/acp-24-6525-2024, https://doi.org/10.5194/acp-24-6525-2024, 2024
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Nitrated aromatic compounds (NACs) and oxygenated derivatives of polycyclic aromatic hydrocarbons (OPAHs) in PM2.5 were examined from an urban area in Beijing during the autumn and winter. The OPAH and NAC concentrations were much higher during heating than before heating. They majorly originated from the combustion of biomass and automobile emissions, and the secondary generation was the major contributor throughout the whole sampling period.
Gregory P. Schill, Karl D. Froyd, Daniel M. Murphy, Christina J. Williamson, Charles Brock, Tomás Sherwen, Mat J. Evans, Eric A. Ray, Eric C. Apel, Rebecca S. Hornbrook, Alan J. Hills, Jeff Peischl, Tomas B. Ryerson, Chelsea R. Thompson, Ilann Bourgeois, Donald R. Blake, Joshua P. DiGangi, and Glenn S. Diskin
EGUsphere, https://doi.org/10.5194/egusphere-2024-1399, https://doi.org/10.5194/egusphere-2024-1399, 2024
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Using single-particle mass spectrometry, we show that trace concentrations of bromine and iodine are ubiquitous in remote tropospheric aerosol, and suggest that aerosols are an important part of the global reactive iodine budget. Comparisons to a global climate model with detailed iodine chemistry are favorable in the background atmosphere; however, the model cannot replicate our measurements near the ocean surface, in biomass burning plumes, and in the stratosphere.
Marco Paglione, David C. S. Beddows, Anna Jones, Thomas Lachlan-Cope, Matteo Rinaldi, Stefano Decesari, Francesco Manarini, Mara Russo, Karam Mansour, Roy M. Harrison, Andrea Mazzanti, Emilio Tagliavini, and Manuel Dall'Osto
Atmos. Chem. Phys., 24, 6305–6322, https://doi.org/10.5194/acp-24-6305-2024, https://doi.org/10.5194/acp-24-6305-2024, 2024
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Applying factor analysis techniques to H-NMR spectra, we present the organic aerosol (OA) source apportionment of PM1 samples collected in parallel at two Antarctic stations, namely Signy and Halley, allowing investigation of aerosol–climate interactions in an unperturbed atmosphere. Our results show remarkable differences between pelagic (open-ocean) and sympagic (sea-ice-influenced) air masses and indicate that various sources and processes are controlling Antarctic aerosols.
Zhichao Dong, Chandra Mouli Pavuluri, Peisen Li, Zhanjie Xu, Junjun Deng, Xueyan Zhao, Xiaomai Zhao, Pingqing Fu, and Cong-Qiang Liu
Atmos. Chem. Phys., 24, 5887–5905, https://doi.org/10.5194/acp-24-5887-2024, https://doi.org/10.5194/acp-24-5887-2024, 2024
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Comprehensive study of optical properties of brown carbon (BrC) in fine aerosols from Tianjin, China, implied that biological emissions are major sources of BrC in summer, whereas fossil fuel combustion and biomass burning emissions are in cold periods. The direct radiation absorption caused by BrC in short wavelengths contributed about 40 % to that caused by BrC in 300–700 nm. Water-insoluble but methanol-soluble BrC contains more protein-like chromophores (PLOM) than that of water-soluble BrC.
Kumiko Goto-Azuma, Yoshimi Ogawa-Tsukagawa, Kaori Fukuda, Koji Fujita, Motohiro Hirabayashi, Remi Dallmayr, Jun Ogata, Nobuhiro Moteki, Tatsuhiro Mori, Sho Ohata, Yutaka Kondo, Makoto Koike, Sumito Matoba, and Teruo Aoki
EGUsphere, https://doi.org/10.5194/egusphere-2024-1498, https://doi.org/10.5194/egusphere-2024-1498, 2024
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Monthly records spanning 350 years from a Greenland ice core reveal trends in black carbon (BC) concentrations and sizes. BC concentrations have risen since the late 19th century due to the inflow of anthropogenic BC, with these particles being larger than those from biomass burning (BB). High BB BC concentration peaks in summer originating from BB could reduce albedo. However, BB BC showed no upward trend until the early 2000s. Our findings are crucial for validating aerosol and climate models.
Shan Wang, Kezheng Liao, Zijing Zhang, Yuk Ying Cheng, Qiongqiong Wang, Hanzhe Chen, and Jian Zhen Yu
Atmos. Chem. Phys., 24, 5803–5821, https://doi.org/10.5194/acp-24-5803-2024, https://doi.org/10.5194/acp-24-5803-2024, 2024
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In this work, hourly primary and secondary organic carbon were estimated by a novel Bayesian inference approach in suburban Hong Kong. Their multi-temporal-scale variations and evolution characteristics during PM2.5 episodes were examined. The methodology could serve as a guide for other locations with similar monitoring capabilities. The observation-based results are helpful for understanding the evolving nature of secondary organic aerosols and refining the accuracy of model simulations.
Andreas Aktypis, Dontavious Sippial, Christina Vasilakopoulou, Angeliki Matrali, Christos Kaltsonoudis, Andrea Simonati, Marco Paglione, Matteo Rinaldi, Stefano Decesari, and Spyros Pandis
EGUsphere, https://doi.org/10.5194/egusphere-2024-1317, https://doi.org/10.5194/egusphere-2024-1317, 2024
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A dual chamber system was deployed in two different environments (Po Valley, Italy and Pertouli forest, Greece) to study the potential of ambient air directly injected into the chambers, to form secondary aerosol. In the Po Valley, the system reacts rapidly forming large amounts of SOA, while in Pertouli the corresponding SOA formation chemistry appears to have been practically terminated before the beginning of most experiments, so there is little additional SOA formation potential left.
Mingfu Cai, Chenshuo Ye, Bin Yuan, Shan Huang, E Zheng, Suxia Yang, Zelong Wang, Yi Lin, Tiange Li, Weiwei Hu, Wei Chen, Qicong Song, Wei Li, Yuwen Peng, Baolin Liang, Qibin Sun, Jun Zhao, Duohong Chen, Jiaren Sun, Zhiyong Yang, and Min Shao
EGUsphere, https://doi.org/10.5194/egusphere-2024-887, https://doi.org/10.5194/egusphere-2024-887, 2024
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This study investigated the daytime secondary organic aerosol (SOA) formation in urban plumes. We observed a significant daytime SOA formation through gas-particle partitioning when the site was affected by urban plumes. Box model simulation indicated that urban pollutants (nitrogen oxide and volatile organic compounds) could enhance the oxidizing capacity, while the elevated volatile organic compounds were mainly responsible for promoting daytime SOA formation.
James Brean, David C. S. Beddows, Eija Asmi, Ari Virkkula, Lauriane L. J. Quéléver, Mikko Sipilä, Floortje Van Den Heuvel, Thomas Lachlan-Cope, Anna Jones, Markus Frey, Angelo Lupi, Jiyeon Park, Young Jun Yoon, Ralf Weller, Giselle L. Marincovich, Gabriela C. Mulena, Roy M. Harrison, and Manuel Dall´Osto
EGUsphere, https://doi.org/10.5194/egusphere-2024-987, https://doi.org/10.5194/egusphere-2024-987, 2024
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Our results emphasize how understanding the geographical variation in surface types across the Antarctic is key to understanding secondary aerosol sources.
Cited articles
Alastuey, A., Querol, X., Castillo, S., Escudero, M., Avila, A., Cuevas, E.,
Torres, C., Romero, P.-M., Exposito, F., García, O., Pedro Diaz, J.,
Dingenen, R. V., and Putaud, J. P.: Characterisation of TSP and PM2.5
at Izaña and Sta. Cruz de Tenerife (Canary Islands, Spain) during a
Saharan Dust Episode (July 2002), Atmos. Environ., 39, 4715–4728,
https://doi.org/10.1016/j.atmosenv.2005.04.018, 2005.
Almeida, S. M., Pio, C. A., Freitas, M. C., Reis, M. A., and Trancoso, M. A.:
Source apportionment of atmospheric urban aerosol based on weekdays/weekend
variability: evaluation of road re-suspended dust contribution, Atmos.
Environ., 40, 2058–2067, https://doi.org/10.1016/j.atmosenv.2005.11.046, 2006a.
Almeida, S. M., Pio, C. A., Freitas, M. C., Reis, M. A., and Trancoso, M. A.:
Approaching PM2.5 and PM2.5−10 source apportionment by
mass balance analysis, principal component analysis and particle size
distribution, Sci. Total Environ., 368, 663–674,
https://doi.org/10.1016/j.scitotenv.2006.03.031, 2006b.
Almeida, S. M., Freitas, M. C., Reis, M., Pinheiro, T., Felix, P. M., and
Pio, C. A.: Fifteen years of nuclear techniques application to suspended
particulate matter studies, J. Radioanal. Nucl. Chem., 297, 347–356,
https://doi.org/10.1007/s10967-012-2354-1, 2013.
Almeida-Silva, M., Almeida, S. M., Freitas, M. C., Pio, C. A., Nunes, T., and
Cardoso, J.: Impact of Sahara dust transport on Cape Verde atmospheric
element particles. J. Toxicol. Env. Heal. A, 76, 240–251,
https://doi.org/10.1080/15287394.2013.757200, 2013.
Almeida-Silva, M., Almeida, S. M., Cardoso, J., Nunes, T., Reis, M. A.,
Chaves, P. C., and Pio, C. A.: Characterization of the aeolian aerosol from
Cape Verde by k(0)-INAA and PIXE, J. Radioanal. Nucl. Chem., 300, 629–635,
https://doi.org/10.1007/s10967-014-2957-9, 2014.
Amato, F. and Hopke, P. K.: Source apportionment of the ambient
PM2.5 across St. Louis using constrained positive matrix
factorization, Atmos. Environ., 46, 329–337,
https://doi.org/10.1016/j.atmosenv.2011.09.062, 2012.
Amato, F., Alastuey, A., Karanasiou, A., Lucarelli, F., Nava, S., Calzolai,
G., Severi, M., Becagli, S., Gianelle, V. L., Colombi, C., Alves, C.,
Custódio, D., Nunes, T., Cerqueira, M., Pio, C., Eleftheriadis, K.,
Diapouli, E., Reche, C., Minguillón, M. C., Manousakas, M.-I., Maggos,
T., Vratolis, S., Harrison, R. M., and Querol, X.: AIRUSE-LIFE+: a harmonized
PM speciation and source apportionment in five southern European cities,
Atmos. Chem. Phys., 16, 3289–3309, https://doi.org/10.5194/acp-16-3289-2016,
2016.
Andrews, E., Saxena, P., Musarra, S., Hildemann, L. M., Koutrakis, P.,
McMurry, P. H., Olmez, I., and White, W. H.: Concentration and Composition of
Atmospheric Aerosols from the 1995 SEAVS Experiment and a Review of the
Closure between Chemical and Gravimetric Measurements, J. Air Waste Manage.
Assoc., 50, 648–664, https://doi.org/10.1080/10473289.2000.10464116, 2000.
Ashbaugh, L. L., Myrup, L. O., and Flocchini, R. G.: A principal component
analysis of sulfur concentrations in the western United States, Atmos.
Environ., 18, 783–791, https://doi.org/10.1016/0004-6981(84)90262-2, 1984.
Belis, C. A., Karagulian, F., Larsen, B. R., and Hopke, P. K.: Critical
review and meta-analysis of ambient particulate matter source apportionment
using receptor models in Europe, Atmos. Environ., 69, 94–108,
https://doi.org/10.1016/j.atmosenv.2012.11.009, 2013.
Belis, C. A., Larsen, B. R., Amato, F., El Haddad, I., Favez, O., Harrison,
R. M., Hopke, P. K., Nava, S., Paatero, P., Prevot, A., Quass, U., Vecchi,
R., and Viana, M.: European Guide on Air Pollution Source Apportionment with
Receptor Models, JRC Reference Report EUR 26080, Publication Office of
the European Union, ISBN 978-92-79-32514-4, https://doi.org/10.2788/9332, 2014.
Blanchard, C.: Methods for attributing ambient air pollutants to emission
sources, Annu. Rev. Energy Environ., 24, 329–365,
https://doi.org/10.1146/annurev.energy.24.1.329, 1999.
Brunekreef, B. and Fosberg, B.: Epidemiological evidence of effects of coarse
airborne particles on health, Eur. Respir. J., 26, 309–318,
https://doi.org/10.1183/09031936.05.00001805, 2005.
Buseck, P. R. and Pósfai, M.: Airborne minerals and related aerosol
particles: Effects on climate and the environment, PNAS, 96, 3372–3379,
https://doi.org/10.1073/pnas.96.7.3372, 1999.
Canepari, S., Farao, C., Marconi, E., Giovannelli, C., and Perrino, C.:
Qualitative and quantitative determination of water in airborne particulate
matter, Atmos. Chem. Phys., 13, 1193–1202,
https://doi.org/10.5194/acp-13-1193-2013, 2013.
Castillo, S., Moreno, T., Querol, X., Alastuey, A., Cuevas, E., Herrmann, L.,
Mounkaila, M., and Gibbons, W.: Trace element variation in size-fractionated
African desert dusts, J. Arid Environ., 72, 1034–1045,
https://doi.org/10.1016/j.jaridenv.2007.12.007, 2008.
Chen, J., Qiu, S., Shang, J., Wilfrid, O. M. F., Liu, X., Tian, H., and Boman
J.: Impact of relative humidity and water soluble constituents of
PM2.5 on visibility impairment in Beijing, China, Aerosol Air Qual.
Res., 14, 260–268, 2014.
Chen, X. and Yu, J. Z.: Measurement of organic mass to organic carbon ratio in
ambient aerosol samples using a gravimetric technique in combination with
chemical analysis, Atmos. Environ., 41, 8857–8864,
https://doi.org/10.1016/j.atmosenv.2007.08.023, 2007.
Chen, L.-W. A. and Cao, J.: PM2.5 Source Apportionment Using a
Hybrid Environmental Receptor, Environ. Sci. Technol., 52, 6357–6369,
https://doi.org/10.1021/acs.est.8b00131, 2018.
Chiapello, I., Bergametti, G., Chatenet, B., Bousquet, P., and Santos Soares,
E.: Origins of African dust transported over northeastern tropical Atlantic,
J. Geophys. Res., 102, 13701–13709, https://doi.org/10.1029/97JD00259, 1997.
Countess, R. J., Wolff, G. T., and Cadle, S. H.: The Denver Winter Aerosol: A
Comprehensive Chemical Characterization, J. Air Pollut. Control Assoc., 30,
1194–1200, https://doi.org/10.1080/00022470.1980.10465167, 1980.
Dick, W. D., Saxena, P., and McMurry, P. H.: Estimation of water uptake by
organic compounds in submicron aerosols measured during the Southeastern
aerosol and visibility study, J. Geophys. Res., 105, 1471–1479,
https://doi.org/10.1029/1999JD901001, 2000.
Eldred, B.: Internal memo to IMPROVE Staff, available at:
http://vista.cira.colostate.edu/improve/Publications/GrayLit/023_SoilEquation/Soil_Eq_Evaluation.pdf
(last access: 30 August 2018), 2003.
Eltayeb, M. A. H., Injuk, J., Maenhaut, W., and Van Grieken, R. E.: Elemental
Composition of Mineral Aerosol Generated from Sudan Sahara Sand, J. Atmos.
Chem., 40, 247–273, https://doi.org/10.1023/A:1012272208129, 2001.
El-Zanan, H. S., Zielinska, B., Mazzoleni, L. R., and Hansen, D. A.:
Analytical determination of the aerosol organic mass-to-organic carbon ratio,
J. Air Waste Manag. Assoc., 59, 58–69, https://doi.org/10.3155/1047-3289.59.1.58, 2009.
Ervens, B., Turpin, B. J., and Weber, R. J.: Secondary organic aerosol
formation in cloud droplets and aqueous particles (aqSOA): a review of
laboratory, field and model studies, Atmos. Chem. Phys., 11, 11069–11102,
https://doi.org/10.5194/acp-11-11069-2011, 2011.
Formenti, P., Andreae, M. O., Lange, L., Roberts, G., Cafineyer, J., Rajta,
I., Maenhaut, W., Holben, B. N., Artaxo, P., and Lelieveld, J.: Saharan dust
in Brazil and Suriname during the Large-Scale Biosphere-Atmosphere Experiment
in Amazonia (LBA) – Cooperative LBA Regional Experiment (CLAIRE) in March
1998, J. Geophys. Res., 106, 14919–14934, https://doi.org/10.1029/2000JD900827, 2001.
Formenti, P., Elbert, W., Maenhaut, W., Haywood, J., and Andrea, M. O.:
Chemical composition of mineral dust aerosol during Saharan Dust Experiment
(SHADE) airborne campaign in the Cape Verde region, September 2000, J.
Geophys Res., 108, 8576, https://doi.org/10.1029/2002JD002648, 2003.
Gama, C., Tchepel, O., Baldasano, J., Basart, S., Ferreira, J., Pio, C.,
Cardoso, J., and Borrego, C.: Seasonal patterns of Saharan dust over Cape
Verde – a combined approach using observations and modelling, Tellus B, 67,
24410, https://doi.org/10.3402/tellusb.v67.24410, 2015.
Genga, A., Ielpo, P., Siciliano, T., and Siciliano, M.: Carbonaceous
particles and aerosol mass closure in PM2.5 collected in a port
city, Atmos. Res., 183, 245–254, https://doi.org/10.1016/j.atmosres.2016.08.022, 2017.
Ginoux, P., Prospero, J. M., Gill, T. E., Hsu, N. C., and Zhao, M.:
Global-scale attribution of anthropogenic and natural dust sources and their
emission rates based on MODIS deep blue aerosol products, Rev. Geophys., 50,
RG3005, https://doi.org/10.1029/2012RG000388, 2012.
Goodman, A. L., Underwood, G. M., and Grassian, V. H.: A laboratory study of
the heterogeneous reaction of nitric acid on calcium carbonate particles, J.
Geophys. Res., 105, 29053–29064, https://doi.org/10.1029/2000JD900396, 2000.
Grigoratos, T., Samara, C., Voutsa, D., Manoli, E., and Kouras, A.: Chemical
composition and mass closure of ambient coarse particles at traffic and
urban-background sites in Thessaloniki, Greece, Environ Sci. Pollut. Res.,
21, 7708–7722, https://doi.org/10.1007/s11356-014-2732-z, 2014.
Guieu, C., Loye-Pilot, M.-D., Ridame, C., and Thomas, C.: Chemical
characterization of the Saharan dust end-member: Some biogeochemical
implications for the western Mediterranean Sea, J. Geophys. Res., 107, D15,
ACH 5-1–ACH 5-11, https://doi.org/10.1029/2001JD000582, 2002.
Guinot, B., Cachier, H., and Oikonomou, K.: Geochemical perspectives from a
new aerosol chemical mass closure, Atmos. Chem. Phys., 7, 1657–1670,
https://doi.org/10.5194/acp-7-1657-2007, 2007.
Harrison, R. M., Jones, A. M., and Lawrence, R. G.: A pragmatic mass closure
model for airborne particulate matter at urban background and roadside sites,
Atmos. Environ., 37, 4927–4933, https://doi.org/10.1016/j.atmosenv.2003.08.025, 2003.
Henry, R. C., Lewis, C. W., Hopke, P. K., and Williamson, H. J.: Review of
receptor model fundamentals, Atmos. Environ., 18, 1507–1515,
https://doi.org/10.1016/0004-6981(84)90375-5, 1984.
Hopke, P. K.: Receptor Modelling in Environmental Chemistry, Wiley & Sons,
NY, 1985.
Japar, S. M., Szkarlat, A. C., Gorse Jr., R. A., Heyerdahl, E. K., Johnson,
R. L., Rau, J. A., and Huntzicker, J. J.: Comparison of Solvent Extraction
and Thermal Optical Carbon Analysis Methods: Application to Diesel Vehicle
Exhaust Aerosol, Environ. Sci. Technol., 18, 231–234,
https://doi.org/10.1021/es00122a004, 1984.
Journet, E., Balkanski, Y., and Harrison, S. P.: A new data set of soil
mineralogy for dust-cycle modeling, Atmos. Chem. Phys., 14, 3801–3816,
https://doi.org/10.5194/acp-14-3801-2014, 2014.
Kandler, K., Schütz, L., Deutscher, C., Eber, M., Hofmann, H.,
Jäckel, S., Jaenicke, R., Knippertz, P., Lieke K., Massling, A., Petzold,
A., Schladitz, A., Weinzierl, B., Wiedensohler, A., Zorn, S., and Weinbruch,
S.: Size distribution, mass concentration, chemical and mineralogical
composition and derived optical parameters of the boundary layer aerosol at
Tinfou, Morocco, during SAMUM 2006, Tellus B, 61, 32–50,
https://doi.org/10.1111/j.1600-0889.2008.00385.x, 2009.
Kitamori, Y., Mochida, M., and Kawamura, K.: Assessment of the aerosol water
content in urban atmospheric particles by the hygroscopic growth measurements
in Sapporo, Japan, Atmos. Environ., 43, 3416–3423,
https://doi.org/10.1016/j.atmosenv.2009.03.037, 2009.
Liu, G. R., Shi, G. L., Tian, Y. Z., Wang, Y. N., Zhang, C. Y., and Feng, Y.
C.: Physically constrained source apportionment (PCSA) for polycyclic
aromatic hydrocarbon using the Multilinear Engine 2-species ratios (ME2-SR)
method, Sci. Total Environ., 502, 16–21,
https://doi.org/10.1016/j.scitotenv.2014.09.011, 2015.
Lohmann, U. and Feichter, J.: Global indirect aerosol effects: a review,
Atmos. Chem. Phys., 5, 715–737, https://doi.org/10.5194/acp-5-715-2005,
2005.
Malm, W. C., Sisler, J. F., Huffman, D., Eldred, R. A., and Cahill, T. A.:
Spatial and seasonal trends in particle concentration and optical extinction
in the United States, J. Geophys. Res., 99, 1347–1370,
https://doi.org/10.1029/93JD02916, 1994.
Mason B. and Moore C. B.: Principles of Geochemistry, 4 Edn., Wiley &
Sons, New York, 1982.
Mirante, F., Salvador, P., Pio, C., Alves, C., Artinano, B., Caseiro, A., and
Revuelta, M. A.: Size fractionated aerosol composition at roadside and
background environments in the Madrid urban atmosphere, Atmos. Res., 138,
278–292, https://doi.org/10.1016/j.atmosres.2013.11.024, 2014.
Moreno, T., Querol, X., Castillo, S., Alastuey, A., and Cuevas, E.:
Geochemical variations in Aeolian mineral particles from the Sahara-Sahel
dust corridor, Chemosphere, 65, 261–270,
https://doi.org/10.1016/j.chemosphere.2006.02.052, 2006.
Nenes, A., Pandis, S. N., and Pilinis, C.: ISORROPIA: A new thermodynamic
equilibrium model for multiphase multicomponent inorganic aerosols, Aquat.
Geoch., 4, 123–152, https://doi.org/10.1023/A:1009604003981, 1998a.
Nenes, A., Pilinis, C., and Pandis, S. N.: Continued Development and Testing
of a New Thermodynamic Aerosol Module for Urban and Regional Air Quality
Models, Atmos. Environ., 33, 1553–1560, https://doi.org/10.1016/S1352-2310(98)00352-5,
1998b.
Paatero, P.: The multilinear engine – a table-driven least squares program
for solving multilinear problems, including the n-way parallel factor
analysis model, J. Comput. Graph Stat., 8, 854–888,
https://doi.org/10.1080/10618600.1999.10474853, 1999.
Paatero, P. and Tapper, U.: Positive matrix factorization: A non-negative
factor model with optimal utilization of error estimates of data values,
Environmetrics, 5, 111–126, https://doi.org/10.1002/env.3170050203, 1994.
Perrino, C., Canepari, S., and Catrambone, M.: Comparing the Performance of
Teflon and Quartz Membrane Filters Collecting Atmospheric PM: Influence of
Atmospheric Water, Aerosol Air Qual. Res., 13, 137–147,
https://doi.org/10.4209/aaqr.2012.07.0167, 2013.
Pio, C., Cerqueira, M., Harrison, R., Nunes, T., Mirante, F., Alves, C.,
Oliveira, C., Sanchez de la Campa, A., Artíñano, B., and Matos, M.:
OC/EC Ratio Observations In Europe: Re-Thinking The Approach For
Apportionment Between Primary And Secondary Organic Carbon, Atmos. Environ.,
45, 6121–6132, https://doi.org/10.1016/j.atmosenv.2011.08.045, 2011.
Pio, C. A. and Lopes, D.: Chlorine loss from marine aerosol in a coastal
atmosphere, J. Geophys. Res., 103, 25263–25269, https://doi.org/10.1029/98JD02088, 1998.
Pio, C. A., Ramos, M. O., and Duarte, A. C.: Measurement of Carbonates in
Atmospheric Aerosols by Acidification and NDIR Analysis of Evolved
CO2, in: Physico-Chemical Behaviour of Atmospheric Pollutants,
edited by: Angeletti, G. and Restelli, G., Report EUR 15609/1 EN, European
Commission, Brussels, Vol. 1, 712–717, 1994.
Pope III, C. A.: Review, Epidemiological basis for particulate air pollution
health standards, Aerosol Sci. Tech., 32, 4–14, https://doi.org/10.1080/027868200303885,
2000.
Pöschl, U.: Atmospheric aerosols: Composition, transformation climate and
health effects, Angew. Chem. Int. Ed., 44, 7520–7540,
https://doi.org/10.1002/anie.200501122, 2005.
Raes, F., Van Dingenen, R., Vignati, E., Wilson, J., Putaud, J. P., Seinfeld,
J. H., and Adams, P.: Formation and cycling of aerosols in the global
troposphere, Atmos. Environ., 34, 4215–4240,
https://doi.org/10.1016/S1352-2310(00)00239-9, 2000.
Ramanathan, V., Crutzen, P. J., Kiehl, J. T., and Rosenfeld, D.: Aerosols,
Climate, and the Hydrological Cycle, Science, 294, 2119–2124,
https://doi.org/10.1126/science.1064034, 2001.
Rees, S. L., Robinson, A. L., Khlystov, A., Stanier, C. O., and Pandis, S.
N.: Mass Balance Closure and the Federal Reference Method for PM2.5
in Pittsburgh, Pennsylvania, Atmos. Environ., 38, 3305–3318,
https://doi.org/10.1016/j.atmosenv.2004.03.016, 2004.
Reff, A., Eberly, S. I., and Bhave, P. V.: Receptor Modeling of Ambient
Particulate Matter Data Using Positive Matrix Factorization: Review of
Existing Methods, J. Air Waste Manag. Assoc., 57, 146–154,
https://doi.org/10.1080/10473289.2007.10465319, 2007.
Remoundaki, E., Papayannis, A., Kassomenos, P., Mantas, E., Kokkalis, P., and
Tsezos, M.: Influence of Saharan Dust Transport Events on PM2.5
Concentrations and Composition over Athens, Water Air Soil Pollut., 224,
1373, https://doi.org/10.1007/s11270-012-1373-4, 2013.
Rogge, W. F., Hildemann, L. M., Mazurek, M. A., Cass, G. R., and Simoneit B.
R. T.: Sources of Fine Organic Aerosol, 4. Particulate Abrasion Products from
Leaf Surfaces of Urban Plants, Environ. Sci. Technol., 27, 2700–2711,
https://doi.org/10.1021/es00049a008, 1993a.
Rogge, W. F., Mazurek, M. A., Hildemann, L. M., and Cass, G. R.:
Quantifcation of Urban Organic Aerosols at a Molecular Level: Identification,
Abundance and Seasonal Variation, Atmos. Environ., 27, 1309–1330,
https://doi.org/10.1016/0960-1686(93)90257-Y, 1993b.
Russel L. M.: Aerosol Organic-Mass-to-Organic-Carbon Ratio Measurements,
Environ. Sci. Technol., 37, 2982–2987, https://doi.org/10.1021/es026123w, 2003.
Salvador, P., Almeida, S. M., Cardoso, J., Almeida-Silva, M., Nunes, T.,
Cerqueira, M., Alves, C., Reis, M. A., Chaves, P. C., Artinano, B., and Pio,
C.: Composition and origin of PM10 in Cape Verde: Characterization
of long-range transport episodes, Atmos. Environ., 127, 326–339,
https://doi.org/10.1016/j.atmosenv.2015.12.057, 2016.
Scheuvens, D., Kandler, K., Ebert, M., and Weinbruch, S.: Bulk composition of
northern African dust and its source sediments – A compilation, Earth-Sci.
Rev., 116, 170–194, https://doi.org/10.1016/j.earscirev.2012.08.005, 2013.
Schuttlefield, J. D., Cox, D., and Grassian, V. H.: An Investigation of water
uptake on Clays Minerals Using ATR-FTIR Spectroscopy Coupled with Quartz
Crystal microbalance measurements, J. Geophys. Res., 112, D21303,
https://doi.org/10.1029/2007JD008973, 2007.
Sciare, J., Oikonomou, K., Cachier, H., Mihalopoulos, N., Andreae, M. O.,
Maenhaut, W., and Sarda-Estève, R.: Aerosol mass closure and
reconstruction of the light scattering coefficient over the Eastern
Mediterranean Sea during the MINOS campaign, Atmos. Chem. Phys., 5,
2253–2265, https://doi.org/10.5194/acp-5-2253-2005, 2005.
Seinfeld, J. H. and Pandis, S. N.: Atmospheric Chemistry and Physics: From
Air Pollution to Climate Change, 2nd Edn., Wiley, Hoboken, NJ, 1998.
Sempere, R. and Kawamura, K.: Comparative Distributions of Dicarboxylic Acids
and Related Polar Compounds in Snow, Rain and Aerosols from Urban Atmosphere,
Atmos. Environ., 28, 449–459, https://doi.org/10.1016/1352-2310(94)90123-6, 1994.
Speer, R. E., Barnes, H. M., and Brown, R.: An instrument for measuring the
liquid content of aerosols, Aerosol Sci. Technol., 27, 50–61,
https://doi.org/10.1080/02786829708965457, 1997.
Speer R. E., Edney E. O., and Kleindienst T. E.: Impact of organic compounds
on the concentrations of liquid water in ambient PM2.5, Aerosol
Science, 34, 63–77, https://doi.org/10.1016/S0021-8502(02)00152-0, 2003.
Stanier, C., Khlystov, A., Chan, W. R., Mandiro, M., and Pandis, S. N.: A
method for the in-situ measurement of aerosol water content of ambient
aerosols: The Dry-Ambient Aerosol Size Spectrometer (DAASS), Aerosol Sci.
Technol., 38, 215–228, https://doi.org/10.1080/02786820390229525, 2004.
Tanaka, T. Y. and Chiba, M.: A numerical study of the contributions of dust
source regions to the global dust budget, Global Planet Change, 52, 88–104,
https://doi.org/10.1016/j.gloplacha.2006.02.002, 2006.
Tang, I. N. and Munkelwitz, H. R.: Water activities, densities, and
refractive indices of aqueous sulfates and sodium nitrate droplets of
atmospheric importance, J. Geophys. Res., 99, 18801–18808,
https://doi.org/10.1029/94JD01345, 1994.
Tang, I. N., Tridico, A. C., and Fung, K. H.: Thermodynamic and optical
properties of sea salt aerosols, J. Geophysical Res., 102, 23269–23275,
https://doi.org/10.1029/97JD01806, 1997.
Tobias, A., Perez, L., Diaz J., Linares, C., Pey, J., Alastuey, A., and
Querol, X.: Short term effects of particulate matter on total mortality
during Saharan dust outbreaks: a case-crossover analysis in Madrid (Spain),
Sci. Total Environ., 412–413, 386–389, https://doi.org/10.1016/j.scitotenv.2011.10.027,
2011.
Tsyro, S. G.: To what extent can aerosol water explain the discrepancy
between model calculated and gravimetric PM10 and PM2.5?,
Atmos. Chem. Phys., 5, 515–532, https://doi.org/10.5194/acp-5-515-2005,
2005.
Turekian, K. K.: Oceans, Prentice-Hall, Englewood Cliffs, NJ, 1968.
Turpin, B. J. and Lim, H. J.: Species Contributions to PM2.5 Mass
Concentrations: Revisiting Common Assumptions for Estimating Organic Mass,
Aerosol Sci. Technol., 35, 602–610, https://doi.org/10.1029/97JD01806, 2001.
Watson, J. G., Zhu, T., Chow, J. C., Engelbrecht, J., Fujita, E. M., and
Wilson, W. E.: Receptor modeling application framework for particle source
apportionment, Chemosphere, 49, 1093–1136,
https://doi.org/10.1016/S0045-6535(02)00243-6, 2002.
Wedepohl, K. H.: The composition of the continental crust, Geochim.
Cosmochim. Ac., 59, 1217–1232, https://doi.org/10.1016/0016-7037(95)00038-2, 1995.
Xu, J., Imre, D., McGraw, R., and Tang, I.: Ammonium sulphate: Equilibrium
and metastability phase diagrams from 40 to −50 ∘C, J. Phys. Res.
B, 102, 7462–7469, https://doi.org/10.1021/jp981929x, 1998.
Short summary
Atmospheric aerosol was sampled in Cabo Verde and analysed for chemical composition. Very high levels of dust were measured during the winter months, as a result of transport from Africa. Mass balances were applied to the particulate material, permitting the determination of seven different source contributions to the aerosol loading. The balance methodology compared favourably with standard source apportionment methods, showing its capability for the source apportionment of aerosol particles.
Atmospheric aerosol was sampled in Cabo Verde and analysed for chemical composition. Very high...
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