Begoña Artíñano Rodríguez De Torres

Dr. Begoña Artíñano Rodríguez De Torres

Department of Environment, CIEMAT, 28040 Madrid, Spain
orcid

Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 December 2004 in Atmospheric Environment
Verified
Journal Article
Closed access
XQXavier Querol
Xavier Querol
Andrés Alastuey UrósAndrés Alastuey Urós
Andrés Alastuey Urós
CRC.R. Ruiz
C.R. Ruiz
Begoña Artíñano Rodríguez De TorresBegoña Artíñano Rodríguez De Torres
Begoña Artíñano Rodríguez De Torres
HHH.C. Hansson
H.C. Hansson
JSJ. Schneider
J. Schneider

1 November 2007 in Atmospheric Environment
Verified
Journal Article
Closed access
XQXavier Querol
Xavier Querol
Mar VianaMar Viana
Mar Viana
Andrés Alastuey UrósAndrés Alastuey Urós
Andrés Alastuey Urós
FAFulvio Amato
Fulvio Amato
TMT. Moreno
T. Moreno
JZJ. Zabalza
J. Zabalza

1 November 2011 in Atmospheric Environment
Verified
Journal Article
Closed access
CPCasimiro Pio
Casimiro Pio
MCMário Cerqueira
Mário Cerqueira
RHRoy M. Harrison
Roy M. Harrison
TNTeresa Nunes
Teresa Nunes
Fátima MiranteFátima Mirante
Fátima Mirante
MMManuel Matos
Manuel Matos

1 June 2008 in Atmospheric Environment
Verified
Journal Article
Closed access
XQXavier Querol
Xavier Querol
Andrés Alastuey UrósAndrés Alastuey Urós
Andrés Alastuey Urós
TMT. Moreno
T. Moreno
Mar VianaMar Viana
Mar Viana
SCSonia Castillo
Sonia Castillo
ACAna María Sánchez de la Campa
Ana María Sánchez de la Campa

1 September 2004 in Journal of Aerosol Science
Verified
Journal Article
Closed access
XQXavier Querol
Xavier Querol
Andrés Alastuey UrósAndrés Alastuey Urós
Andrés Alastuey Urós
Mar VianaMar Viana
Mar Viana
Sergio RodríguezSergio Rodríguez
Sergio Rodríguez
Begoña Artíñano Rodríguez De TorresBegoña Artíñano Rodríguez De Torres
Begoña Artíñano Rodríguez De Torres
JGJ.I. Gil
J.I. Gil

28 May 2015 in Atmospheric Chemistry and Physics
Verified
Journal Article
Open access
PDF file
MBM. Brines
M. Brines
MDM. Dall'Osto
M. Dall'Osto
DBD. C. S. Beddows
D. C. S. Beddows
Roy HarrisonRoy Harrison
Roy Harrison
FGF. Gómez-Moreno
F. Gómez-Moreno
XQXavier Querol
Xavier Querol
Road traffic emissions are often considered the main source of ultrafine particles (UFP, diameter smaller than 100 nm) in urban environments. However, recent studies worldwide have shown that – in high-insolation urban regions at least – new particle formation events can also contribute to UFP. In order to quantify such events we systematically studied three cities located in predominantly sunny environments: Barcelona (Spain), Madrid (Spain) and Brisbane (Australia). Three long-term data sets (1–2 years) of fine and ultrafine particle number size distributions (measured by SMPS, Scanning Mobility Particle Sizer) were analysed. Compared to total particle number concentrations, aerosol size distributions offer far more information on the type, origin and atmospheric evolution of the particles. By applying k-means clustering analysis, we categorized the collected aerosol size distributions into three main categories: "Traffic" (prevailing 44–63% of the time), "Nucleation" (14–19%) and "Background pollution and Specific cases" (7–22%). Measurements from Rome (Italy) and Los Angeles (USA) were also included to complement the study. The daily variation of the average UFP concentrations for a typical nucleation day at each site revealed a similar pattern for all cities, with three distinct particle bursts. A morning and an evening spike reflected traffic rush hours, whereas a third one at midday showed nucleation events. The photochemically nucleated particles' burst lasted 1–4 h, reaching sizes of 30–40 nm. On average, the occurrence of particle size spectra dominated by nucleation events was 16% of the time, showing the importance of this process as a source of UFP in urban environments exposed to high solar radiation. Nucleation events lasting for 2 h or more occurred on 55% of the days, this extending to > 4 h in 28% of the days, demonstrating that atmospheric conditions in urban environments are not favourable to the growth of photochemically nucleated particles. In summary, although traffic remains the main source of UFP in urban areas, in developed countries with high insolation urban nucleation events are also a main source of UFP. If traffic-related particle concentrations are reduced in the future, nucleation events will likely increase in urban areas, due to the reduced urban condensation sinks.