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dc.contributor.authorTilmes, Simone
dc.contributor.authorEmmons, Louisa
dc.contributor.authorGarcia-Menendez, Fernando
dc.contributor.authorBrown-Steiner, Benjamin E
dc.contributor.authorSelin, Noelle E
dc.contributor.authorPrinn, Ronald G
dc.contributor.authorMonier, Erwan
dc.date.accessioned2018-09-06T15:36:25Z
dc.date.available2018-09-06T15:36:25Z
dc.date.issued2018-06
dc.date.submitted2018-05
dc.identifier.issn1680-7324
dc.identifier.issn1680-7316
dc.identifier.urihttp://hdl.handle.net/1721.1/117646
dc.description.abstractThe detection of meteorological, chemical, or other signals in modeled or observed air quality data - such as an estimate of a temporal trend in surface ozone data, or an estimate of the mean ozone of a particular region during a particular season - is a critical component of modern atmospheric chemistry. However, the magnitude of a surface air quality signal is generally small compared to the magnitude of the underlying chemical, meteorological, and climatological variabilities (and their interactions) that exist both in space and in time, and which include variability in emissions and surface processes. This can present difficulties for both policymakers and researchers as they attempt to identify the influence or signal of climate trends (e.g., any pauses in warming trends), the impact of enacted emission reductions policies (e.g., United States NOxState Implementation Plans), or an estimate of the mean state of highly variable data (e.g., summertime ozone over the northeastern United States). Here we examine the scale dependence of the variability of simulated and observed surface ozone data within the United States and the likelihood that a particular choice of temporal or spatial averaging scales produce a misleading estimate of a particular ozone signal. Our main objective is to develop strategies that reduce the likelihood of overconfidence in simulated ozone estimates. We find that while increasing the extent of both temporal and spatial averaging can enhance signal detection capabilities by reducing the noise from variability, a strategic combination of particular temporal and spatial averaging scales can maximize signal detection capabilities over much of the continental US. For signals that are large compared to the meteorological variability (e.g., strong emissions reductions), shorter averaging periods and smaller spatial averaging regions may be sufficient, but for many signals that are smaller than or comparable in magnitude to the underlying meteorological variability, we recommend temporal averaging of 10-15 years combined with some level of spatial averaging (up to several hundred kilometers). If this level of averaging is not practical (e.g., the signal being examined is at a local scale), we recommend some exploration of the spatial and temporal variability to provide context and confidence in the robustness of the result. These results are consistent between simulated and observed data, as well as within a single model with different sets of parameters. The strategies selected in this study are not limited to surface ozone data and could potentially maximize signal detection capabilities within a broad array of climate and chemical observations or model output.en_US
dc.description.sponsorshipUnited States. Department of Energy (Grant DE-FG02-94ER61937)en_US
dc.publisherCopernicus Publicationsen_US
dc.relation.isversionofhttp://dx.doi.org/10.5194/acp-18-8373-2018en_US
dc.rightsCreative Commons Attribution 4.0 International Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourceCopernicus Publicationsen_US
dc.titleMaximizing ozone signals among chemical, meteorological, and climatological variabilityen_US
dc.typeArticleen_US
dc.identifier.citationBrown-Steiner, Benjamin et al. “Maximizing Ozone Signals Among Chemical, Meteorological, and Climatological Variability.” Atmospheric Chemistry and Physics 18, 11 (June 2018): 8373–8388 © 2018 Author(s)en_US
dc.contributor.departmentMassachusetts Institute of Technology. Center for Global Change Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Earth, Atmospheric, and Planetary Sciencesen_US
dc.contributor.departmentMassachusetts Institute of Technology. Joint Program on the Science & Policy of Global Changeen_US
dc.contributor.mitauthorBrown-Steiner, Benjamin E
dc.contributor.mitauthorSelin, Noelle E
dc.contributor.mitauthorPrinn, Ronald G
dc.contributor.mitauthorMonier, Erwan
dc.relation.journalAtmospheric Chemistry and Physicsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2018-08-28T12:22:52Z
dspace.orderedauthorsBrown-Steiner, Benjamin; Selin, Noelle E.; Prinn, Ronald G.; Monier, Erwan; Tilmes, Simone; Emmons, Louisa; Garcia-Menendez, Fernandoen_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-6396-5622
dc.identifier.orcidhttps://orcid.org/0000-0001-5925-3801
dc.identifier.orcidhttps://orcid.org/0000-0001-5533-6570
mit.licensePUBLISHER_CCen_US


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