I. Nuaaman
Environment Canada
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Featured researches published by I. Nuaaman.
Science | 2012
Christopher D. Cappa; Timothy B. Onasch; Paola Massoli; Douglas R. Worsnop; T. S. Bates; Eben S. Cross; P. Davidovits; Jani Hakala; K. Hayden; B. T. Jobson; Katheryn R. Kolesar; D. A. Lack; Shao-Meng Li; Daniel Mellon; I. Nuaaman; Jason S. Olfert; Tuukka Petäjä; Patricia K. Quinn; Chen Song; R. Subramanian; Eric J. Williams; Rahul A. Zaveri
Dark Forcing Soot, or black carbon, is a ubiquitous atmospheric pollutant whose warming effect might be second only to carbon dioxide. When black carbon is emitted, it combines with other aerosols to form heterogeneous mixtures. Models have predicted that internal mixing of black carbon with other materials can double the amount of radiation absorbed. Cappa et al. (p. 1078) report that in situ measurements of the enhancement of radiation absorption by these mixed black carbon–containing particles in the atmosphere show a much smaller effect. Thus, many climate models may be overestimating the amount of warming caused by black carbon emissions. Direct measurements show that ambient atmospheric particulate black carbon absorbs less solar radiation than theory suggested. Atmospheric black carbon (BC) warms Earth’s climate, and its reduction has been targeted for near-term climate change mitigation. Models that include forcing by BC assume internal mixing with non-BC aerosol components that enhance BC absorption, often by a factor of ~2; such model estimates have yet to be clearly validated through atmospheric observations. Here, direct in situ measurements of BC absorption enhancements (Eabs) and mixing state are reported for two California regions. The observed Eabs is small—6% on average at 532 nm—and increases weakly with photochemical aging. The Eabs is less than predicted from observationally constrained theoretical calculations, suggesting that many climate models may overestimate warming by BC. These ambient observations stand in contrast to laboratory measurements that show substantial Eabs for BC are possible.
Environmental Science & Technology | 2011
D. A. Lack; Christopher D. Cappa; Justin M. Langridge; Roya Bahreini; Gina Buffaloe; C. A. Brock; K. Cerully; D. J. Coffman; Katherine Hayden; John S. Holloway; Paola Massoli; Shao-Meng Li; Robert McLaren; Ann M. Middlebrook; R. H. Moore; Athanasios Nenes; I. Nuaaman; Timothy B. Onasch; J. Peischl; A. E. Perring; Patricia K. Quinn; T. B. Ryerson; Joshua P. Schwartz; Ryan Spackman; Steven C. Wofsy; D. R. Worsnop; B. Xiang; Eric Williams
Atmospheric emissions of gas and particulate matter from a large ocean-going container vessel were sampled as it slowed and switched from high-sulfur to low-sulfur fuel as it transited into regulated coastal waters of California. Reduction in emission factors (EFs) of sulfur dioxide (SO₂), particulate matter, particulate sulfate and cloud condensation nuclei were substantial (≥ 90%). EFs for particulate organic matter decreased by 70%. Black carbon (BC) EFs were reduced by 41%. When the measured emission reductions, brought about by compliance with the California fuel quality regulation and participation in the vessel speed reduction (VSR) program, are placed in a broader context, warming from reductions in the indirect effect of SO₄ would dominate any radiative changes due to the emissions changes. Within regulated waters absolute emission reductions exceed 88% for almost all measured gas and particle phase species. The analysis presented provides direct estimations of the emissions reductions that can be realized by California fuel quality regulation and VSR program, in addition to providing new information relevant to potential health and climate impact of reduced fuel sulfur content, fuel quality and vessel speed reductions.
Journal of Geophysical Research | 2012
T. S. Bates; Patricia K. Quinn; Amanda A. Frossard; Lynn M. Russell; Jani Hakala; Tuukka Petäjä; Markku Kulmala; David S. Covert; Christopher D. Cappa; S.-M. Li; K. L. Hayden; I. Nuaaman; Robert McLaren; Paola Massoli; Manjula R. Canagaratna; Timothy B. Onasch; Donna Sueper; D. R. Worsnop; William C. Keene
Atmospheric Chemistry and Physics | 2013
Christopher D. Cappa; Eric J. Williams; D. A. Lack; Gina Buffaloe; D. J. Coffman; K. L. Hayden; Scott C. Herndon; S.-M. Li; Paola Massoli; Robert McLaren; I. Nuaaman; Timothy B. Onasch; Patricia K. Quinn
Atmospheric Chemistry and Physics | 2013
Gina Buffaloe; D. A. Lack; Eric J. Williams; D. J. Coffman; K. L. Hayden; S.-M. Li; I. Nuaaman; Paola Massoli; Timothy B. Onasch; Patricia K. Quinn; Christopher D. Cappa
Science | 2013
Christopher D. Cappa; Timothy B. Onasch; Paola Massoli; Douglas R. Worsnop; T. S. Bates; Eben S. Cross; P. Davidovits; Jani Hakala; K. Hayden; B. T. Jobson; Katheryn R. Kolesar; D. A. Lack; Shao-Meng Li; Daniel Mellon; I. Nuaaman; Jason N. Olfert; Tuukka Petäjä; Patricia K. Quinn; Chen Song; R. Subramanian; Eric J. Williams; Rahul A. Zaveri
Atmospheric Chemistry and Physics | 2015
I. Nuaaman; S.-M. Li; K. L. Hayden; Timothy B. Onasch; Paola Massoli; Donna Sueper; D. R. Worsnop; T. S. Bates; Patricia K. Quinn; Robert McLaren
Journal of Geophysical Research | 2012
T. S. Bates; Patricia K. Quinn; Amanda A. Frossard; Lynn M. Russell; Jani Hakala; Tuukka Petäjä; Markku Kulmala; David S. Covert; Christopher D. Cappa; S.-M. Li; Katherine Hayden; I. Nuaaman; Robert McLaren; Paola Massoli; Manjula R. Canagaratna; Timothy B. Onasch; Donna Sueper; D. R. Worsnop; William C. Keene
Archive | 2008
I. Nuaaman; Robert A. McLaren; Andrew Y. Ng; Alla A. Kornilova; Sophie Moukhtar
AAAR 30th Annual Conference. | 2011
Paola Massoli; Timothy B. Onasch; I. Nuaaman; Shao-Meng Li; Katherine Hayden; Donna Sueper; Christopher D. Cappa; Jani Hakala; T. S. Bates; Patricia K. Quinn; Douglas R. Worsnop