Mostrar el registro sencillo del ítem

dc.contributor.author
Pineda Rojas, Andrea Laura  
dc.contributor.author
Bikiel, Damian Ezequiel  
dc.date.available
2021-01-07T12:34:06Z  
dc.date.issued
2019-09  
dc.identifier.citation
Pineda Rojas, Andrea Laura; Bikiel, Damian Ezequiel; Global and local sensitivity analysis of urban background ozone modelled with a simplified photochemical scheme; Pergamon-Elsevier Science Ltd; Atmospheric Environment; 213; 9-2019; 199-206  
dc.identifier.issn
1352-2310  
dc.identifier.uri
http://hdl.handle.net/11336/121699  
dc.description.abstract
The Generic Reaction Set (GRS) is a simplified photochemical scheme that allows estimation of ozone (O3) concentrations resulting from nitrogen oxides (NOx) and reactive organic compounds (ROC) emissions in an urban area. Due to its simplicity and relative good performance, it has been included in the algorithms of many atmospheric dispersion models. However, few works assess quantitatively the sensitivity of simulated O3 concentrations to the uncertainty in the GRS input variables. In order to do so, in this work we carry out two sensitivity analyses: global (applying an atmospheric dispersion model to a representative real case) and local (using a box-GRS model under a wide range of hypothetical conditions). In the global study, a Monte Carlo analysis is performed to estimate the uncertainty of maximum O3 concentrations that is caused by possible errors in the GRS input variables, applying the DAUMOD-GRS model in the Metropolitan Area of Buenos Aires. Results show that the initial concentration of O3 dominates at all analysed receptors while that of NOx can make a non-negligible contribution if its error is relatively large. In order to further analyse the effect of each parameter individually, a local sensitivity analysis is performed using a box-GRS model under a wide range of conditions. Except for the small NOx-limited region, sensitivity indexes computed for +-1 ppb changes in the initial concentrations of ROC, NOx and O3 are in the ranges 0.00-0.35, 0.00-0.81 and 0.05-0.96, respectively, with that of ozone dominating over most of the isopleth diagram space. In turn, its relative impact increases with decreasing ROC initial concentrations. Reaction rate coefficients have also different effects on O3 peak concentrations depending on the initial conditions of the system. Our results show quantitatively the change of dominant variables under different environments.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Pergamon-Elsevier Science Ltd  
dc.rights
info:eu-repo/semantics/restrictedAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
AIR QUALITY MODELS  
dc.subject
GENERIC REACTION SET  
dc.subject
OZONE  
dc.subject
SENSITIVITY ANALYSIS  
dc.subject
URBAN SCALE  
dc.subject.classification
Meteorología y Ciencias Atmosféricas  
dc.subject.classification
Ciencias de la Tierra y relacionadas con el Medio Ambiente  
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS  
dc.title
Global and local sensitivity analysis of urban background ozone modelled with a simplified photochemical scheme  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2020-11-13T20:47:08Z  
dc.identifier.eissn
1873-2844  
dc.journal.volume
213  
dc.journal.pagination
199-206  
dc.journal.pais
Países Bajos  
dc.journal.ciudad
Amsterdam  
dc.description.fil
Fil: Pineda Rojas, Andrea Laura. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones del Mar y la Atmósfera. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Centro de Investigaciones del Mar y la Atmósfera; Argentina  
dc.description.fil
Fil: Bikiel, Damian Ezequiel. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina  
dc.journal.title
Atmospheric Environment  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://linkinghub.elsevier.com/retrieve/pii/S1352231019303978  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.atmosenv.2019.06.014