Show simple item record

dc.contributor.authorKoss, Abigail R.
dc.contributor.authorNihill, Kevin J.
dc.contributor.authorLim, Christopher Yung-Ta
dc.contributor.authorRowe, James Clifford.
dc.contributor.authorKroll, Jesse
dc.date.accessioned2020-06-02T16:51:03Z
dc.date.available2020-06-02T16:51:03Z
dc.date.issued2020-01
dc.identifier.issn1680-7316
dc.identifier.urihttps://hdl.handle.net/1721.1/125614
dc.description.abstractOxidation of organic compounds in the atmosphere produces an immensely complex mixture of product species, posing a challenge for both their measurement in laboratory studies and their inclusion in air quality and climate models. Mass spectrometry techniques can measure thousands of these species, giving insight into these chemical processes, but the datasets themselves are highly complex. Data reduction techniques that group compounds in a chemically and kinetically meaningful way provide a route to simplify the chemistry of these systems but have not been systematically investigated. Here we evaluate three approaches to reducing the dimensionality of oxidation systems measured in an environmental chamber: positive matrix factorization (PMF), hierarchical clustering analysis (HCA), and a parameterization to describe kinetics in terms of multigenerational chemistry (gamma kinetics parameterization, GKP). The evaluation is implemented by means of two datasets: synthetic data consisting of a three-generation oxidation system with known rate constants, generation numbers, and chemical pathways; and the measured products of OH-initiated oxidation of a substituted aromatic compound in a chamber experiment. We find that PMF accounts for changes in the average composition of all products during specific periods of time but does not sort compounds into generations or by another reproducible chemical process. HCA, on the other hand, can identify major groups of ions and patterns of behavior and maintains bulk chemical properties like carbon oxidation state that can be useful for modeling. The continuum of kinetic behavior observed in a typical chamber experiment can be parameterized by fitting species' time traces to the GKP, which approximates the chemistry as a linear, first-order kinetic system. The fitted parameters for each species are the number of reaction steps with OH needed to produce the species (the generation) and an effective kinetic rate constant that describes the formation and loss rates of the species. The thousands of species detected in a typical laboratory chamber experiment can be organized into a much smaller number (10-30) of groups, each of which has a characteristic chemical composition and kinetic behavior. This quantitative relationship between chemical and kinetic characteristics, and the significant reduction in the complexity of the system, provides an approach to understanding broad patterns of behavior in oxidation systems and could be exploited for mechanism development and atmospheric chemistry modeling.en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (Grant AGS-1638672)en_US
dc.description.sponsorshipErwin-Schrödinger-Stipendium (Grant J-3900)en_US
dc.language.isoen
dc.publisherCopernicus GmbHen_US
dc.relation.isversionofhttps://dx.doi.org/10.5194/acp-20-1021-2020en_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceCopernicus Publicationsen_US
dc.titleDimensionality-reduction techniques for complex mass spectrometric datasets: Application to laboratory atmospheric organic oxidation experimentsen_US
dc.typeArticleen_US
dc.identifier.citationKoss, Abigail R. et al. “Dimensionality-reduction techniques for complex mass spectrometric datasets: Application to laboratory atmospheric organic oxidation experiments.” Atmospheric Chemistry and Physics 20 (2020): 1021-1041 © 2020 The Author(s)en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Civil and Environmental Engineeringen_US
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.updated2020-03-24T13:43:31Z
dspace.date.submission2020-03-24T13:43:33Z
mit.journal.volume20en_US
mit.journal.issue2en_US
mit.licensePUBLISHER_CC
mit.metadata.statusComplete


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record