D. Baumgardner
National Autonomous University of Mexico
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Featured researches published by D. Baumgardner.
Atmospheric Research | 2001
D. Baumgardner; Haflidi H. Jonsson; W Dawson; D O'Connor; R Newton
A new airborne particle spectrometer has been developed with the same measurement capabilities of the Forward Scattering Spectrometer Probes (FSSP) models 100 and 300 (FSSP-300 and FSSP-100), two-dimensional optical imaging probe (2D-OAP), the Multiangle Aerosol Spectrometer Probe (MASP) and hot-wire liquid water probe, but with a single integrated system. The cloud, aerosol and precipitation spectrometer (CAPS) measures particles from 0.35 μm to 1.55 mm in diameter and liquid water content (LWC) from 0.01 to 3 g m -3 . In addition to combining five probes into one, it measures airspeed at the sample volume and transmits a data stream that requires no special interfaces to communicate with most computers.
Atmospheric Environment | 2001
Graciela B. Raga; D. Baumgardner; T. Castro; Amparo Martínez-Arroyo; Rafael Navarro-González
Mexico City, one of the largest cities in the world, has a major problem with high levels of anthropogenic gases and aerosols. Some facets of this problem have been studied through measurements made during the past 40 years. These measurements are reviewed and evaluated with respect to physical processes that underlie the primary and secondary formation of gases and aerosols, their spatial and temporal evolution as well as their potential impact on the local and regional environment. Past measurements are heavily biased towards certain locations and time periods, and are of limited use for understanding fundamental processes that govern the formation and evolution of the principal pollutants. Recommendations are made whereby the measurement database could be expanded to better represent the characteristics of Mexico City gases and aerosols and to contribute to mitigation strategies that would lessen the environmental impact of these pollutants. # 2001 Elsevier Science Ltd. All rights reserved.
Journal of Geophysical Research | 2004
Shan-Hu Lee; J. C. Wilson; D. Baumgardner; R. L. Herman; Elliot M. Weinstock; Bernard G. Lafleur; Gregory L. Kok; Bruce E. Anderson; P. Lawson; B. Baker; Anthony W. Strawa; J. V. Pittman; Jeanne M. Reeves; T. P. Bui
[1] Previous studies show that new particle formation takes place in the outflows of marine stratus and cumulus clouds. Here we show measurements of high concentrations of ultrafine particles, diameters (Dp) from 4 to 9 nm (N4–9), in interstitial cloud aerosol. These ultrafine particles indicate that in situ new particle formation occurs interstitially in cirrus clouds. Measurements were made at altitudes from 7 to 16 km over Florida with instruments on the WB-57F aircraft during Cirrus Regional Study of Tropical Anvils and Cirrus Layers-Florida Area Cirrus Experiments (CRYSTAL-FACE) in July 2002. Sizeresolved ice crystal particle concentrations and water vapor concentrations were measured to help identify the presence of cirrus clouds. About 72% of the in-cloud samples showed new particle formation events with the average N4–9 of 3.0 10 3 cm 3 , whereas about 56% of the out-of-cloud samples had events with the lower N4–9of 1.3 10 3 cm 3 . The periods during which high N4–9 appeared were often associated with times of increasing ice water content (IWC) and high relative humidity with respect to ice (RHI); however, the measured N4–9was not quantitatively correlated to IWC. The magnitude and frequency of new particle formation events seen in cirrus clouds were also higher than those previously observed in the tropical/subtropical upper troposphere in the absence of clouds. These results suggest that cirrus clouds may provide favorable conditions for particle formation, such as low temperatures, high RHI, high OH production (due to high water vapor), cloud electricity, and atmospheric convection. At present, however, particle formation mechanisms in clouds are unidentified. INDEX TERMS: 0305 Atmospheric Composition and Structure: Aerosols and particles (0345, 4801); 0320 Atmospheric Composition and Structure: Cloud physics and chemistry; 0335 Atmospheric Composition and Structure: Ion chemistry of the atmosphere (2419, 2427); 0365 Atmospheric Composition and Structure: Troposphere—composition and chemistry; 0368 Atmospheric Composition and Structure: Troposphere—constituent transport and chemistry;
Bulletin of the American Meteorological Society | 2012
D. Baumgardner; Linnea M. Avallone; Aaron Bansemer; St. Borrmann; P. R. A. Brown; Ulrich Bundke; Patrick Y. Chuang; Daniel J. Cziczo; P. R. Field; Martin Gallagher; Jean-François Gayet; Andrew J. Heymsfield; A. Korolev; Martina Krämer; Greg M. McFarquhar; S. Mertes; O. Möhler; S. Lance; P. Lawson; D. Petters; Kerri A. Pratt; G. C. Roberts; D. C. Rogers; O. Stetzer; Jeffrey L. Stith; W. Strapp; Cynthia H. Twohy; Manfred Wendisch
A meeting of 31 international experts on in situ measurements from aircraft was held to identify unresolved questions concerning ice formation and evolution in ice clouds, assess the current state of instrumentation that can address these problems, introduce emerging technology that may overcome current measurement issues and recommend future courses of action that can improve our understanding of ice cloud microphysical processes and their impact on the environment. The meeting proceedings and outcome has been described in detail in a manuscript submitted to the Bulletin of the American Meteorological Society (BAMS) on March 24, 2011. This paper is currently under review. The remainder of this summary, in the following pages, is the text of the BAMS article. A technical note that will be published by the National Center for Atmospheric Research is currently underway and is expected to be published before the end of the year.
Environmental Research Letters | 2008
D. Baumgardner; G Kok; Martina Krämer; F Weidle
In situ measurements have been made in the upper troposphere of the properties of particles containing light absorbing carbon (LAC). These measurements, made in late November 2006 over northern Europe, show that the average LAC mass concentration varies between 1 and 5 ng m−3 over a latitude range 50° to 70°N, with maxima at 50° and 66°. The relative fraction of all particles larger than 0.1 µm that contain LAC decreases at higher latitudes. The derived extinction coefficient, which also increases with latitude, reaches a maximum of 1.4 Mm−1 at 66°. The air mass histories associated with the LAC were evaluated with back trajectory analysis using wind field analysis from the European Center for Median-Range Weather Forecast (ECMWF). A positive correlation exists between the fraction of particles containing LAC and the maximum relative humidity (RH), minimum temperature and maximum number of hours of cloud experienced by the air mass in the 5–10 days prior to being sampled by the aircraft. Air masses arriving from lower altitudes and with trajectories over North America also had larger concentration fractions of LAC. The average LAC mass is in good agreement with previous measurements made over North America for the same latitude range, and the span of values fits best with model predictions of LAC distributions that assume that the LAC transported from surface sources is hydrophobic.
Reference Module in Earth Systems and Environmental Sciences#R##N#Encyclopedia of Atmospheric Sciences (Second Edition) | 2015
D. Baumgardner; J.-F. Gayet; A. Korolev; C. Twohy; J. Fugal
The impact of clouds on weather and climate is determined by their microphysical properties (i.e., the size distribution, water content, optical properties, and shape). Understanding how these properties evolve requires detailed studies with in situ measurements using a suite of different sensors. This article gives an overview of the different techniques that are used to determine these cloud characteristics and examples of some of the types of information that can be extracted from these data.
Atmosfera | 2013
Diana Pozo; Julio C. Marín; Graciela B. Raga; D. Baumgardner
A number of studies have explored the effect of anthropogenic emissions on the development and evolution of precipitation in different types of clouds; however, the magnitude of the effect is still not clear, particularly for the case of deep, mixed-phase clouds. In this study, changes in the parameterization of the autoconversion process were introduced in the Advanced Regional Prediction System (ARPS) model to further evaluate this Atmosfera 26(2), 221-241 (2013)question. The simulations were initialized with cloud droplet distributions measured from an instrumented C-130 aircraft flying 600-800 km offshore in the intertropical convergence zone during the East Pacific Investigations of Climate (EPIC) project. Two contrasting cases were selected, one with and the other without the influence of anthropogenic aerosols. The simulations indicate that the increased cloud condensation nuclei (CCN) concentrations lead to a delay in the formation of rain and to a decrease in precipitation that reaches the surface as a result of the inhibition of the autoconversion of cloud water to rain water and the subsequent delay in the formation of hail. In addition, hail forms at higher levels in the cloud for the case of anthropogenic CCN. The most important process in the production of rain water in both cases is the melting of hail. A decrease in the mass of hail that falls below the freezing level in the polluted case, leads to a decrease in the resulting precipitation at the surface. Changes in the initial concentration of CCN do not appear to influence the storm strength in terms of updrafts and cloud top height, suggesting little sensitivity of the cloud dynamics. A control case simulation using the old microphysics scheme produces much more precipitation than either of the clean and polluted cases. In addition, the clean case with the modified parameterization shows a better agreement to observations than the control case. It is suggested to use the new scheme to simulate deep convective development over tropical maritime regions.
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 Measurement Techniques | 2012
D. Baumgardner; Olga B. Popovicheva; J. D. Allan; V. Bernardoni; J. Cao; F. Cavalli; J. Cozic; Evangelia Diapouli; Kostas Eleftheriadis; P. J. Genberg; C. Gonzalez; M. Gysel; A. John; Thomas W. Kirchstetter; Thomas A. J. Kuhlbusch; M. Laborde; D. A. Lack; T. Müller; Reinhard Niessner; Andreas Petzold; A. Piazzalunga; J.-P. Putaud; Joshua P. Schwarz; Patrick J. Sheridan; R. Subramanian; Erik Swietlicki; G. Valli; R. Vecchi; Mar Viana
Atmospheric Chemistry and Physics | 2010
Karl D. Froyd; D. M. Murphy; P. Lawson; D. Baumgardner; R. L. Herman