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Andréa Dde Almeida Castanho
,
Paulo Artaxo
,
J. Vanderlei Martins
,
Peter V. Hobbs
,
Lorraine Remer
,
Marcia Yamasoe
, and
Peter R. Colarco

Abstract

The Chesapeake Lighthouse and Aircraft Measurements for Satellites (CLAMS) experiment was carried out off the central East Coast of the United States in July 2001. During CLAMS, aerosol particle mass was measured at two ground stations and on the University of Washington’s Convair 580 research aircraft. Physical and chemical characteristics of the aerosols were identified and quantified. Three main aerosol regimes were identified in the region and are discussed in this work: local pollution/sea salt background, long-range transported dust, and long-range transported pollution. The major component measured in the fine mode of the aerosol on the ground at Wallops Island, Virginia, was sulfate, estimated as NH4HSO4, which accounted for 55% ± 9% on average of the fine particle mass (FPM) during the experiment period. Black carbon concentrations accounted for 3% ± 1% of FPM; soil dust was also present, representing on average 6% ± 8% of FPM. The difference between the sum of the masses of the measured compounds and the total fine particle mass was 36% ± 10% of FPM, which is attributed primarily to nitrates and organic carbon that were not measured. Aerosol chemical composition in the atmospheric column is also discussed and compared with ground-based measurements. Aerosol dust concentration reached 40% of FPM during an incursion of Saharan dust between 24 and 26 July. Sulfate aerosol reached 70% of FPM during the transport of regional pollution on 17 July. Moderate Resolution Imaging Spectroradiometer (MODIS) aerosol optical thickness, coupled with air parcel back trajectories, supported the conclusion of episodes of long-range transport of dust from the Sahara Desert and pollutants from the continental United States.

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Sachin Patade
,
Vaughan T. J. Phillips
,
Pierre Amato
,
Heinz G. Bingemer
,
Susannah M. Burrows
,
Paul J. DeMott
,
Fabio L. T. Goncalves
,
Daniel A. Knopf
,
Cindy E. Morris
,
Carl Alwmark
,
Paulo Artaxo
,
Christopher Pöhlker
,
Jann Schrod
, and
Bettina Weber

Abstract

To resolve the various types of biological ice nuclei (IN) with atmospheric models, an extension of the empirical parameterization (EP) is proposed to predict the active IN from multiple groups of primary biological aerosol particles (PBAPs). Our approach is to utilize coincident observations of PBAP sizes, concentrations, biological composition, and ice nucleating ability. The parameterization organizes PBAPs into five basic groups: 1) fungal spores, 2) bacteria, 3) pollen, 4) viral particles, plant/animal detritus, 5) algae, and their respective fragments. This new biological component of the EP was constructed by fitting predicted concentrations of PBAP IN to those observed at the Amazon Tall Tower Observatory (ATTO) site located in the central Amazon. The fitting parameters for pollen and viral particles and plant/animal detritus, which are much less active as IN than fungal and bacterial groups, are constrained based on their ice nucleation activity from the literature. The parameterization has empirically derived dependencies on the surface area of each group (except algae), and the effects of variability in their mean sizes and number concentrations are represented via their influences on surface area. The concentration of active algal IN is estimated from literature-based measurements. Predictions of this new biological component of the EP are consistent with previous laboratory and field observations not used in its construction. The EP scheme was implemented in a 0D parcel model. It confirms that biological IN account for most of the total IN activation at temperatures warmer than −20°C and at colder temperatures dust and soot become increasingly more important to ice nucleation.

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Federico Bianchi
,
Victoria A. Sinclair
,
Diego Aliaga
,
Qiaozhi Zha
,
Wiebke Scholz
,
Cheng Wu
,
Liine Heikkinen
,
Rob Modini
,
Eva Partoll
,
Fernando Velarde
,
Isabel Moreno
,
Yvette Gramlich
,
Wei Huang
,
Alkuin Maximilian Koenig
,
Markus Leiminger
,
Joonas Enroth
,
Otso Peräkylä
,
Angela Marinoni
,
Chen Xuemeng
,
Luis Blacutt
,
Ricardo Forno
,
Rene Gutierrez
,
Patrick Ginot
,
Gaëlle Uzu
,
Maria Cristina Facchini
,
Stefania Gilardoni
,
Martin Gysel-Beer
,
Runlong Cai
,
Tuukka Petäjä
,
Matteo Rinaldi
,
Harald Saathoff
,
Karine Sellegri
,
Douglas Worsnop
,
Paulo Artaxo
,
Armin Hansel
,
Markku Kulmala
,
Alfred Wiedensohler
,
Paolo Laj
,
Radovan Krejci
,
Samara Carbone
,
Marcos Andrade
, and
Claudia Mohr

Abstract

This paper presents an introduction to the Southern Hemisphere High Altitude Experiment on Particle Nucleation and Growth (SALTENA). This field campaign took place between December 2017 and June 2018 (wet to dry season) at Chacaltaya (CHC), a GAW (Global Atmosphere Watch) station located at 5,240 m MSL in the Bolivian Andes. Concurrent measurements were conducted at two additional sites in El Alto (4,000 m MSL) and La Paz (3,600 m MSL). The overall goal of the campaign was to identify the sources, understand the formation mechanisms and transport, and characterize the properties of aerosol at these stations. State-of-the-art instruments were brought to the station complementing the ongoing permanent GAW measurements, to allow a comprehensive description of the chemical species of anthropogenic and biogenic origin impacting the station and contributing to new particle formation. In this overview we first provide an assessment of the complex meteorology, airmass origin, and boundary layer–free troposphere interactions during the campaign using a 6-month high-resolution Weather Research and Forecasting (WRF) simulation coupled with Flexible Particle dispersion model (FLEXPART). We then show some of the research highlights from the campaign, including (i) chemical transformation processes of anthropogenic pollution while the air masses are transported to the CHC station from the metropolitan area of La Paz–El Alto, (ii) volcanic emissions as an important source of atmospheric sulfur compounds in the region, (iii) the characterization of the compounds involved in new particle formation, and (iv) the identification of long-range-transported compounds from the Pacific or the Amazon basin. We conclude the article with a presentation of future research foci. The SALTENA dataset highlights the importance of comprehensive observations in strategic high-altitude locations, especially the undersampled Southern Hemisphere.

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Manfred Wendisch
,
Ulrich Pöschl
,
Meinrat O. Andreae
,
Luiz A. T. Machado
,
Rachel Albrecht
,
Hans Schlager
,
Daniel Rosenfeld
,
Scot T. Martin
,
Ahmed Abdelmonem
,
Armin Afchine
,
Alessandro C. Araùjo
,
Paulo Artaxo
,
Heinfried Aufmhoff
,
Henrique M. J. Barbosa
,
Stephan Borrmann
,
Ramon Braga
,
Bernhard Buchholz
,
Micael Amore Cecchini
,
Anja Costa
,
Joachim Curtius
,
Maximilian Dollner
,
Marcel Dorf
,
Volker Dreiling
,
Volker Ebert
,
André Ehrlich
,
Florian Ewald
,
Gilberto Fisch
,
Andreas Fix
,
Fabian Frank
,
Daniel Fütterer
,
Christopher Heckl
,
Fabian Heidelberg
,
Tilman Hüneke
,
Evelyn Jäkel
,
Emma Järvinen
,
Tina Jurkat
,
Sandra Kanter
,
Udo Kästner
,
Mareike Kenntner
,
Jürgen Kesselmeier
,
Thomas Klimach
,
Matthias Knecht
,
Rebecca Kohl
,
Tobias Kölling
,
Martina Krämer
,
Mira Krüger
,
Trismono Candra Krisna
,
Jost V. Lavric
,
Karla Longo
,
Christoph Mahnke
,
Antonio O. Manzi
,
Bernhard Mayer
,
Stephan Mertes
,
Andreas Minikin
,
Sergej Molleker
,
Steffen Münch
,
Björn Nillius
,
Klaus Pfeilsticker
,
Christopher Pöhlker
,
Anke Roiger
,
Diana Rose
,
Dagmar Rosenow
,
Daniel Sauer
,
Martin Schnaiter
,
Johannes Schneider
,
Christiane Schulz
,
Rodrigo A. F. de Souza
,
Antonio Spanu
,
Paul Stock
,
Daniel Vila
,
Christiane Voigt
,
Adrian Walser
,
David Walter
,
Ralf Weigel
,
Bernadett Weinzierl
,
Frank Werner
,
Marcia A. Yamasoe
,
Helmut Ziereis
,
Tobias Zinner
, and
Martin Zöger

Abstract

Between 1 September and 4 October 2014, a combined airborne and ground-based measurement campaign was conducted to study tropical deep convective clouds over the Brazilian Amazon rain forest. The new German research aircraft, High Altitude and Long Range Research Aircraft (HALO), a modified Gulfstream G550, and extensive ground-based instrumentation were deployed in and near Manaus (State of Amazonas). The campaign was part of the German–Brazilian Aerosol, Cloud, Precipitation, and Radiation Interactions and Dynamics of Convective Cloud Systems–Cloud Processes of the Main Precipitation Systems in Brazil: A Contribution to Cloud Resolving Modeling and to the GPM (Global Precipitation Measurement) (ACRIDICON– CHUVA) venture to quantify aerosol–cloud–precipitation interactions and their thermodynamic, dynamic, and radiative effects by in situ and remote sensing measurements over Amazonia. The ACRIDICON–CHUVA field observations were carried out in cooperation with the second intensive operating period of Green Ocean Amazon 2014/15 (GoAmazon2014/5). In this paper we focus on the airborne data measured on HALO, which was equipped with about 30 in situ and remote sensing instruments for meteorological, trace gas, aerosol, cloud, precipitation, and spectral solar radiation measurements. Fourteen research flights with a total duration of 96 flight hours were performed. Five scientific topics were pursued: 1) cloud vertical evolution and life cycle (cloud profiling), 2) cloud processing of aerosol particles and trace gases (inflow and outflow), 3) satellite and radar validation (cloud products), 4) vertical transport and mixing (tracer experiment), and 5) cloud formation over forested/deforested areas. Data were collected in near-pristine atmospheric conditions and in environments polluted by biomass burning and urban emissions. The paper presents a general introduction of the ACRIDICON– CHUVA campaign (motivation and addressed research topics) and of HALO with its extensive instrument package, as well as a presentation of a few selected measurement results acquired during the flights for some selected scientific topics.

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