Literature DB >> 33777125

Dimensionality-reduction techniques for complex mass spectrometric datasets: application to laboratory atmospheric organic oxidation experiments.

Abigail R Koss1, Manjula R Canagaratna2, Alexander Zaytsev3, Jordan E Krechmer2, Martin Breitenlechner3, Kevin J Nihill1, Christopher Y Lim1, James C Rowe1, Joseph R Roscioli2, Frank N Keutsch3, Jesse H Kroll1.   

Abstract

Oxidation 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.

Entities:  

Year:  2020        PMID: 33777125      PMCID: PMC7995644          DOI: 10.5194/acp-20-1021-2020

Source DB:  PubMed          Journal:  Atmos Chem Phys        ISSN: 1680-7316            Impact factor:   6.133


  19 in total

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2.  Kinetic analysis of sequential multistep reactions.

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Journal:  J Phys Chem B       Date:  2007-11-10       Impact factor: 2.991

3.  Evaluation of a New Reagent-Ion Source and Focusing Ion-Molecule Reactor for Use in Proton-Transfer-Reaction Mass Spectrometry.

Authors:  Jordan Krechmer; Felipe Lopez-Hilfiker; Abigail Koss; Manuel Hutterli; Carsten Stoermer; Benjamin Deming; Joel Kimmel; Carsten Warneke; Rupert Holzinger; John Jayne; Douglas Worsnop; Katrin Fuhrer; Marc Gonin; Joost de Gouw
Journal:  Anal Chem       Date:  2018-10-01       Impact factor: 6.986

4.  Secondary organic aerosol formation from acyclic, monocyclic, and polycyclic alkanes.

Authors:  James F Hunter; Anthony J Carrasquillo; Kelly E Daumit; Jesse H Kroll
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5.  Recent Discoveries and Future Challenges in Atmospheric Organic Chemistry.

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6.  The atmospheric oxidation mechanism of 1,2,4-trimethylbenzene initiated by OH radicals.

Authors:  Yun Li; Liming Wang
Journal:  Phys Chem Chem Phys       Date:  2014-09-07       Impact factor: 3.676

7.  The statistical evolution of multiple generations of oxidation products in the photochemical aging of chemically reduced organic aerosol.

Authors:  Kevin R Wilson; Jared D Smith; Sean H Kessler; Jesse H Kroll
Journal:  Phys Chem Chem Phys       Date:  2011-12-12       Impact factor: 3.676

8.  Carbon oxidation state as a metric for describing the chemistry of atmospheric organic aerosol.

Authors:  Jesse H Kroll; Neil M Donahue; Jose L Jimenez; Sean H Kessler; Manjula R Canagaratna; Kevin R Wilson; Katye E Altieri; Lynn R Mazzoleni; Andrew S Wozniak; Hendrik Bluhm; Erin R Mysak; Jared D Smith; Charles E Kolb; Douglas R Worsnop
Journal:  Nat Chem       Date:  2011-01-09       Impact factor: 24.427

9.  An iodide-adduct high-resolution time-of-flight chemical-ionization mass spectrometer: application to atmospheric inorganic and organic compounds.

Authors:  Ben H Lee; Felipe D Lopez-Hilfiker; Claudia Mohr; Theo Kurtén; Douglas R Worsnop; Joel A Thornton
Journal:  Environ Sci Technol       Date:  2014-05-21       Impact factor: 9.028

10.  Using collision-induced dissociation to constrain sensitivity of ammonia chemical ionization mass spectrometry ( N H 4 + CIMS) to oxygenated volatile organic compounds.

Authors:  Alexander Zaytsev; Martin Breitenlechner; Abigail R Koss; Christopher Y Lim; James C Rowe; Jesse H Kroll; Frank N Keutsch
Journal:  Atmos Meas Tech       Date:  2019-03-20       Impact factor: 4.176

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  1 in total

1.  Nontarget Screening Exhibits a Seasonal Cycle of PM2.5 Organic Aerosol Composition in Beijing.

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Journal:  Environ Sci Technol       Date:  2022-03-18       Impact factor: 11.357

  1 in total

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