J. P. Schwarz
Cooperative Institute for Research in Environmental Sciences
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Featured researches published by J. P. Schwarz.
Aerosol Science and Technology | 2010
J. P. Schwarz; J. R. Spackman; R. S. Gao; A. E. Perring; Eilene S. Cross; Timothy B. Onasch; Alexander Ahern; William Wrobel; P. Davidovits; Jason S. Olfert; Manvendra K. Dubey; Claudio Mazzoleni; D. W. Fahey
A single particle soot photometer (SP2) uses an intense laser to heat individual aerosol particles of refractory black carbon (rBC) to vaporization, causing them to emit detectable amounts of thermal radiation that are used to quantify rBC mass. This approach is well suited for the detection of the majority of rBC mass loading in the ambient atmosphere, which occurs primarily in the accumulation mode (∼ 1–300 fg-rBC/particle). In addition to operator choices about instrument parameters, SP2 detection of rBC number and/or mass can be limited by the physical process inherent in the SP2 detection technique — namely at small rBC mass or low laser intensities, particles fail to heat to vaporization, a requirement for proper detection. In this study, the SP2s ability to correctly detect and count individual flame-generated soot particles was measured at different laser intensities for different rBC particle masses. The flame-generated soot aerosol used for testing was optionally prepared with coatings of organic and non-organic material and/or thermally denuded. These data are used to identify a minimum laser intensity for accurate detection at sea level of total rBC mass in the accumulation mode (300 nW/(220-nm PSL)), a minimum rBC mass (∼ 0.7-fg rBC-mass corresponding to 90 nm volume-equivalent diameter) for near-unity number detection efficiency with a typical operating laser intensity (450 nW/(220-nm PSL)), and a methodology using observed color temperature to recognize laser intensity insufficient for accurate rBC mass detection. Additionally, methods for measurement of laser intensity using either laboratory or ambient aerosol are presented.
Scientific Reports | 2013
J. P. Schwarz; R. S. Gao; A. E. Perring; J. R. Spackman; D. W. Fahey
The effect of anthropogenic black carbon (BC) aerosol on snow is of enduring interest due to its consequences for climate forcing. Until now, too little attention has been focused on BCs size in snow, an important parameter affecting BC light absorption in snow. Here we present first observations of this parameter, revealing that BC can be shifted to larger sizes in snow than are typically seen in the atmosphere, in part due to the processes associated with BC removal from the atmosphere. Mie theory analysis indicates a corresponding reduction in BC absorption in snow of 40%, making BC size in snow the dominant source of uncertainty in BCs absorption properties for calculations of BCs snow albedo climate forcing. The shift reduces estimated BC global mean snow forcing by 30%, and has scientific implications for our understanding of snow albedo and the processing of atmospheric BC aerosol in snowfall.
Aerosol Science and Technology | 2013
R. S. Gao; A. E. Perring; Troy Thornberry; Andrew W. Rollins; J. P. Schwarz; Steven J. Ciciora; D. W. Fahey
We report the design of a small optical particle counter with high sensitivity and low construction cost for atmospheric aerosol measurements. Particle sensing is based on the detection of the forward scattering of laser light. The separation of the laser beam and scattered light is achieved with a novel yet simple optical system. A laboratory prototype system with a 405-nm laser and photomultiplier tube detector has successfully detected polystyrene latex particles as small as 125 nm in diameter with unit efficiency. Theoretical calculations suggest that a lower detectable size limit of 100 nm can be achieved with reduction of background scattered light. The new counter will be useful in a variety of ground-based as well as small balloon-borne applications such as vertical profiling and in situ measurement of particles from explosive volcanic eruptions. Copyright 2013 American Association for Aerosol Research
Aerosol Science and Technology | 2018
B. Mason; Nicholas L. Wagner; G. Adler; E. Andrews; C. A. Brock; Timothy D. Gordon; D. A. Lack; A. E. Perring; Mathews S. Richardson; J. P. Schwarz; M. A. Shook; K. L. Thornhill; Luke D. Ziemba; D. M. Murphy
Abstract During the SEAC4RS campaign in 2013, inflight measurements of light-absorption by aerosol in biomass burning and agriculture fire plumes were collected along with concomitant measurements of aerosol extinction, scattering, and black carbon mass concentration. Here, we compare three measurements of aerosol absorption coefficients: from a photoacoustic spectrometer (PAS), a particle soot absorption photometer (PSAP), and a continuous light absorption photometer (CLAP). Each of these absorption measurements was collected in three visible spectral regions: red, green, and blue (although the precise wavelength and bandwidth vary with each instrument). The absorption measurements were compared during the plumes, in the boundary layer, and in the free troposphere. The slopes from the comparison ranged from 0.6 to 1.24. For biomass burning plumes, the uncertainty in the absorption measurements translates into a range in single scattering albedos of 0.93–0.94 at a wavelength of 660 nm, 0.94–0.95 at 532 nm and 0.92–0.95 at 405 nm. Overall, the aerosol absorption instruments agreed within their stated accuracies. Comparisons with simultaneous measurements of refractive black carbon mass concentration (collected by a single particle soot photometer), were used to derive the mass absorption coefficients (MAC). For all wavelengths, the MAC was high by greater than a factor of three compared to the expected MAC for black carbon.
Atmospheric Chemistry and Physics | 2009
D. Koch; Michael Schulz; Stefan Kinne; Tami C. Bond; Yves Balkanski; Susanne E. Bauer; Terje K. Berntsen; Olivier Boucher; Mian Chin; Antony D. Clarke; F. Dentener; T. Diehl; Richard C. Easter; D. W. Fahey; Johann Feichter; D. Fillmore; S. Freitag; Steven J. Ghan; Paul Ginoux; S. L. Gong; Larry W. Horowitz; Trond Iversen; A. Kirkevåg; Z. Klimont; Yutaka Kondo; M. Krol; Xiaohong Liu; Cameron Stuart McNaughton; Ron L. Miller; V. Montanaro
Geophysical Research Letters | 2009
Carsten Warneke; R. Bahreini; J. Brioude; C. A. Brock; J. A. de Gouw; D. W. Fahey; Karl D. Froyd; John S. Holloway; Ann M. Middlebrook; Libby Miller; Stephen A. Montzka; D. M. Murphy; J. Peischl; T. B. Ryerson; J. P. Schwarz; J. R. Spackman; P. R. Veres
Journal of Geophysical Research | 2008
J. P. Schwarz; J. R. Spackman; D. W. Fahey; R. S. Gao; Ulrike Lohmann; P. Stier; L. A. Watts; D. S. Thomson; D. A. Lack; Leonhard Pfister; M. J. Mahoney; D. Baumgardner; J. C. Wilson; Jeanne M. Reeves
Atmospheric Chemistry and Physics | 2009
Gunnar Myhre; Tore F. Berglen; Mona Johnsrud; C. R. Hoyle; Terje K. Berntsen; Sundar A. Christopher; D. W. Fahey; Ivar S. A. Isaksen; Thomas A. Jones; Ralph A. Kahn; Norman G. Loeb; Patricia K. Quinn; Lorraine A. Remer; J. P. Schwarz; Karl Espen Yttri
Geophysical Research Letters | 2011
T. B. Ryerson; K. C. Aikin; Wayne M. Angevine; E. Atlas; D. R. Blake; C. A. Brock; F. C. Fehsenfeld; R. S. Gao; J. A. de Gouw; D. W. Fahey; John S. Holloway; D. A. Lack; R. A. Lueb; Simone Meinardi; Ann M. Middlebrook; D. M. Murphy; J. A. Neuman; J. B. Nowak; D. D. Parrish; J. Peischl; A. E. Perring; Ilana B. Pollack; A. R. Ravishankara; James M. Roberts; J. P. Schwarz; J. R. Spackman; Harald Stark; Carsten Warneke; L. A. Watts
Atmospheric Chemistry and Physics | 2012
G. W. Mann; Kenneth S. Carslaw; David A. Ridley; D. V. Spracklen; K. J. Pringle; Joonas Merikanto; Hannele Korhonen; J. P. Schwarz; L. A. Lee; P. T. Manktelow; Matthew T. Woodhouse; Anja Schmidt; Thomas J. Breider; K. M. Emmerson; C. L. Reddington; M. P. Chipperfield; S. J. Pickering
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Cooperative Institute for Research in Environmental Sciences
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