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Special Issue for the 9th International Conference on Carbonaceous Particles in the Atmosphere

Description: Carbonaceous particles are a minor constituent of the atmosphere but have a profound effect on air quality, human health, visibility and climate. The importance of carbonaceous particles has been increasingly recognized and become a mainstream topic at numerous conferences. Such was not the case in 1978, when the 1st International Conference on Carbonaceous Particles in the Atmosphere (ICCPA), or ''Carbon Conference'' as it is widely known, was introduced as a new forum to bring together scientists who were just beginning to reveal the importance and complexity of carbonaceous particles in the environment. Table 1 lists the conference dates, venues in the series as well as the proceedings, and special issues resulting form the meetings. Penner and Novakov (Penner and Novakov, 1996) provide an excellent historical perspective to the early ICCPA Conferences. Thirty years later, the ninth in this conference series was held at its inception site, Berkeley, California, attended by 160 scientists from 31 countries, and featuring both new and old themes in 49 oral and 83 poster presentations. Topics covered such areas as historical trends in black carbon aerosol, ambient concentrations, analytic techniques, secondary aerosol formation, biogenic, biomass, and HULIS1 characterization, optical properties, and regional and global climate effects. The conference website, http://iccpa.lbl.gov/, holds the agenda, as well as many presentations, for the 9th ICCPA. The 10th ICCPA is tentatively scheduled for 2011 in Vienna, Austria. The papers in this issue are representative of several of the themes discussed in the conference. Ban-Weiss et al., (Ban-Weiss et al., accepted) measured the abundance of ultrafine particles in a traffic tunnel and found that heavy duty diesel trucks emit at least an order of magnitude more ultrafine particles than light duty gas-powered vehicles per unit of fuel burned. Understanding of this issue is important as ultrafine particles have been shown to ...
Date: December 11, 2009
Creator: Strawa, A.W.; Kirchstetter, T.W. & Puxbaum, H.
Partner: UNT Libraries Government Documents Department

Measured Black Carbon Deposition on the Sierra Nevada Snow Pack and Implication for Snow Pack Retreat

Description: Modeling studies show that the darkening of snow and ice by black carbon deposition is a major factor for the rapid disappearance of arctic sea ice, mountain glaciers and snow packs. This study provides one of the first direct measurements for the efficient removal of black carbon from the atmosphere by snow and its subsequent deposition to the snow packs of California. The early melting of the snow packs in the Sierras is one of the contributing factors to the severe water problems in California. BC concentrations in falling snow were measured at two mountain locations and in rain at a coastal site. All three stations reveal large BC concentrations in precipitation, ranging from 1.7 ng/g to 12.9 ng/g. The BC concentrations in the air after the snow fall were negligible suggesting an extremely efficient removal of BC by snow. The data suggest that below cloud scavenging, rather than ice nuclei, was the dominant source of BC in the snow. A five-year comparison of BC, dust, and total fine aerosol mass concentrations at multiple sites reveals that the measurements made at the sampling sites were representative of large scale deposition in the Sierra Nevada. The relative concentration of iron and calcium in the mountain aerosol indicates that one-quarter to one-third of the BC may have been transported from Asia.
Date: January 12, 2010
Creator: Hadley, O.L.; Corrigan, C.E.; Kirchstetter, T.W.; Cliff, S.S. & Ramanathan, V.
Partner: UNT Libraries Government Documents Department

Modified thermal-optical analysis using spectral absorption selectivity to distinguish black carbon from pyrolized organic carbon

Description: Black carbon (BC), a main component of combustion-generated soot, is a strong absorber of sunlight and contributes to climate change. Measurement methods for BC are uncertain, however. This study presents a method for analyzing the BC mass loading on a quartz fiber filter using a modified thermal-optical analysis method, wherein light transmitted through the sample is measured over a spectral region instead of at a single wavelength as the sample is heated. Evolution of the spectral light transmission signal depends on the relative amounts of light-absorbing BC and char, the latter of which forms when organic carbon in the sample pyrolyzes during heating. Absorption selectivities of BC and char are found to be distinct and are used to apportion the amount of light attenuated by each component in the sample. Light attenuation is converted to mass concentration based on derived mass attenuation efficiencies (MAE) of BC and char. The fraction of attenuation due to each component are scaled by their individual MAE values and added together as the total mass of light absorbing carbon (LAC). An iterative algorithm is used to find the MAE values for both BC and char that provide the best fit to the carbon mass remaining on the filter (derived from direct measurements of thermally evolved CO{sub 2}) at temperatures higher than 480 C. This method was applied to measure the BC concentration in precipitation samples collected from coastal and mountain sites in Northern California. The uncertainty in measured BC concentration of samples that contained a high concentration of organics susceptible to char ranged from 12 to 100 percent, depending on the mass loading of BC on the filter. The lower detection limit for this method was approximately 0.35 {micro}g BC and uncertainty approached 20 percent for BC mass loading greater than 1.0 {micro}g BC.
Date: April 14, 2008
Creator: Hadley, Odelle; Hadley, O.L.; Corrigan, C.E. & Kirchstetter, T.W.
Partner: UNT Libraries Government Documents Department

Response of California temperature to regional anthropogenic aerosol changes

Description: In this paper, we compare constructed records of concentrations of black carbon (BC)--an indicator of anthropogenic aerosols--with observed surface temperature trends in California. Annual average BC concentrations in major air basins in California significantly decreased after about 1990, coincident with an observed statewide surface temperature increase. Seasonal aerosol concentration trends are consistent with observed seasonal temperature trends. These data suggest that the reduction in anthropogenic aerosol concentrations contributed to the observed surface temperature increase. Conversely, high aerosol concentrations may lower surface temperature and partially offset the temperature increase of greenhouse gases.
Date: May 12, 2008
Creator: Kirchstetter, Thomas; Novakov, T.; Kirchstetter, T.W.; Menon, S. & Aguiar, J.
Partner: UNT Libraries Government Documents Department

Aerosol organic carbon to black carbon ratios: Analysis ofpublished data and implications for climate forcing

Description: Measurements of organic carbon (OC) and black carbon (BC)concentrations over a variety of locations worldwide, have been analyzed to infer the spatial distributions of the ratios of OC to BC. Since these ratios determine the relative amounts of scattering and absorption, they are often used to estimate the radiative forcing due to aerosols. An artifact in the protocol for filter measurements of OC has led to widespread overestimates of the ratio of OC to BC in atmospheric aerosols. We developed a criterion to correct for this artifact and analyze corrected OC to BC ratios. The OC to BC ratios, ranging from 1.3to 2.4, appear relatively constant and are generally unaffected by seasonality, sources or technology changes, at the locations considered here. The ratios compare well with emission inventories over Europe and China but are a factor of two lower in other regions. The reduced estimate for OC/BC in aerosols strengthens the argument that reduction of soot emissions maybe a useful approach to slow global warming.
Date: July 11, 2005
Creator: Novakov, T.; Menon, S.; Kirchstetter, T.W.; Koch, D. & Hansen, J.E.
Partner: UNT Libraries Government Documents Department

Trends in on-road vehicle emissions of ammonia

Description: Motor vehicle emissions of ammonia have been measured at a California highway tunnel in the San Francisco Bay area. Between 1999 and 2006, light-duty vehicle ammonia emissions decreased by 38 {+-} 6%, from 640 {+-} 40 to 400 {+-} 20 mg kg{sup -1}. High time resolution measurements of ammonia made in summer 2001 at the same location indicate a minimum in ammonia emissions correlated with slower-speed driving conditions. Variations in ammonia emission rates track changes in carbon monoxide more closely than changes in nitrogen oxides, especially during later evening hours when traffic speeds are highest. Analysis of remote sensing data of Burgard et al. (Environ Sci. Technol. 2006, 40, 7018-7022) indicates relationships between ammonia and vehicle model year, nitrogen oxides, and carbon monoxide. Ammonia emission rates from diesel trucks were difficult to measure in the tunnel setting due to the large contribution to ammonia concentrations in a mixed-traffic bore that were assigned to light-duty vehicle emissions. Nevertheless, it is clear that heavy-duty diesel trucks are a minor source of ammonia emissions compared to light-duty gasoline vehicles.
Date: July 15, 2008
Creator: Kean, A.J.; Littlejohn, D.; Ban-Weiss, G.A.; Harley, R.A.; Kirchstetter, T.W. & Lunden, M. M.
Partner: UNT Libraries Government Documents Department

Large historical changes of fossil-fuel black carbon aerosols

Description: Anthropogenic emissions of fine black carbon (BC) particles, the principal light-absorbing atmospheric aerosol, have varied during the past century in response to changes of fossil-fuel utilization, technology developments, and emission controls. We estimate historical trends of fossil-fuel BC emissions in six regions that represent about two-thirds of present day emissions and extrapolate these to global emissions from 1875 onward. Qualitative features in these trends show rapid increase in the latter part of the 1800s, the leveling off in the first half of the 1900s, and the re-acceleration in the past 50 years as China and India developed. We find that historical changes of fuel utilization have caused large temporal change in aerosol absorption, and thus substantial change of aerosol single scatter albedo in some regions, which suggests that BC may have contributed to global temperature changes in the past century. This implies that the BC history needs to be represented realistically in climate change assessments.
Date: September 26, 2002
Creator: Novakov, T.; Ramanathan, V.; Hansen, J.E.; Kirchstetter, T.W.; Sato, M.; Sinton, J.E. et al.
Partner: UNT Libraries Government Documents Department

Indoor, outdoor and regional profiles of PM2.5 sulfate, nitrateand carbon

Description: Fine particle concentrations were measured simultaneously at three locations: a regional monitoring site in Fresno, California, a backyard of an unoccupied residence in Clovis, California located 6 km northeast of the regional site; and indoors at the same residence. Measurements included 10-min determination of PM{sub 2.5} nitrate, sulfate and carbon using an automated collection and vaporization system, and black carbon measured by light attenuation through a filter deposit. Specific outdoor PM{sub 2.5} constituents were compared to assess the appropriateness of using regional data to model indoor concentrations from outdoor sources. The outdoor data show that, in general, the regional results provide a good representation of the concentrations seen at the building exterior. The indoor concentrations showed considerable attenuation as well as a broadening and time-lag for the concentration peaks. The concentration reduction was the largest for PM{sub 2.5} nitrate, which appears to undergo phase changes in addition to indoor deposition and penetration losses.
Date: January 31, 2002
Creator: Hering, S. V.; Lunden, M. M.; Kirchstetter, T. W.; Thatcher, T. L.; Revzan, K. L.; Sextro, R. G. et al.
Partner: UNT Libraries Government Documents Department

Optical and Physical Properties from Primary On-Road Vehicle ParticleEmissions And Their Implications for Climate Change

Description: During the summers of 2004 and 2006, extinction and scattering coefficients of particle emissions inside a San Francisco Bay Area roadway tunnel were measured using a combined cavity ring-down and nephelometer instrument. Particle size distributions and humidification were also measured, as well as several gas phase species. Vehicles in the tunnel traveled up a 4% grade at a speed of approximately 60 km h{sup -1}. The traffic situation in the tunnel allows the apportionment of emission factors between light duty gasoline vehicles and diesel trucks. Cross-section emission factors for optical properties were determined for the apportioned vehicles to be consistent with gas phase and particulate matter emission factors. The absorption emission factor (the absorption cross-section per mass of fuel burned) for diesel trucks (4.4 {+-} 0.79 m{sup 2} kg{sup -1}) was 22 times larger than for light-duty gasoline vehicles (0.20 {+-} 0.05 m{sup 2} kg{sup -1}). The single scattering albedo of particles - which represents the fraction of incident light that is scattered as opposed to absorbed - was 0.2 for diesel trucks and 0.3 for light duty gasoline vehicles. These facts indicate that particulate matter from motor vehicles exerts a positive (i.e., warming) radiative climate forcing. Average particulate mass absorption efficiencies for diesel trucks and light duty gasoline vehicles were 3.14 {+-} 0.88 m{sup 2} g{sub PM}{sup -1} and 2.9 {+-} 1.07 m{sup 2} g{sub PM}{sup -1}, respectively. Particle size distributions and optical properties were insensitive to increases in relative humidity to values in excess of 90%, reinforcing previous findings that freshly emitted motor vehicle particulate matter is hydrophobic.
Date: January 23, 2009
Creator: Strawa, A.W.; Kirchstetter, T.W.; Hallar, A.G.; Ban-Weiss, G.A.; McLaughlin, J.P.; Harley, R.A. et al.
Partner: UNT Libraries Government Documents Department