Raymond M. Hoff

Bio: Raymond M. Hoff is an academic researcher from University of Maryland, Baltimore County. The author has contributed to research in topics: Lidar & Air quality index. The author has an hindex of 37, co-authored 95 publications receiving 5999 citations. Previous affiliations of Raymond M. Hoff include University of Maryland, Baltimore & National Water Research Institute.

THE CALIPSO MISSION: A Global 3D View of Aerosols and Clouds

Abstract: Aerosols and clouds have important effects on Earth's climate through their effects on the radiation budget and the cycling of water between the atmosphere and Earth's surface. Limitations in our understanding of the global distribution and properties of aerosols and clouds are partly responsible for the current uncertainties in modeling the global climate system and predicting climate change. The CALIPSO satellite was developed as a joint project between NASA and the French space agency CNES to provide needed capabilities to observe aerosols and clouds from space. CALIPSO carries CALIOP, a two-wavelength, polarization-sensitive lidar, along with two passive sensors operating in the visible and thermal infrared spectral regions. CALIOP is the first lidar to provide long-term atmospheric measurements from Earth's orbit. Its profiling and polarization capabilities offer unique measurement capabilities. Launched together with the CloudSat satellite in April 2006 and now flying in formation with the A-train satellite constellation, CALIPSO is now providing information on the distribution and properties of aerosols and clouds, which is fundamental to advancing our understanding and prediction of climate. This paper provides an overview of the CALIPSO mission and instruments, the data produced, and early results.

Remote sensing of particulate pollution from space: have we reached the promised land?

Abstract: The recent literature on satellite remote sensing of air quality is reviewed. 2009 is the 50th anniversary of the first satellite atmospheric observations. For the first 40 of those years, atmospheric composition measurements, meteorology, and atmospheric structure and dynamics dominated the missions launched. Since 1995, 42 instruments relevant to air quality measurements have been put into orbit. Trace gases such as ozone, nitric oxide, nitrogen dioxide, water, oxygen/tetraoxygen, bromine oxide, sulfur dioxide, formaldehyde, glyoxal, chlorine dioxide, chlorine monoxide, and nitrate radical have been measured in the stratosphere and troposphere in column measurements. Aerosol optical depth (AOD) is a focus of this review and a significant body of literature exists that shows that ground-level fine particulate matter (PM2.5) can be estimated from columnar AOD. Precision of the measurement of AOD is +/-20% and the prediction of PM2.5 from AOD is order +/-30% in the most careful studies. The air quality needs that can use such predictions are examined. Satellite measurements are important to event detection, transport and model prediction, and emission estimation. It is suggested that ground-based measurements, models, and satellite measurements should be viewed as a system, each component of which is necessary to better understand air quality.

Validation of the Saharan dust plume conceptual model using lidar, meteosat, and ECMWF Data

Abstract: Lidar observations collected during the Lidar In-space Technology Experiment experiment in conjunction with the Meteosat and European Centre for Medium-Range Weather Forecasts data have been used not only to validate the Saharan dust plume conceptual model constructed from the GARP (Global Atmospheric Research Programme) Atlantic Tropical Experiment data, but also to examine the vicissitudes of the Saharan aerosol including their optical depths across the west Africa and east Atlantic regions. Optical depths were evaluated from both the Meteosat and lidar data. Back trajectory calculations were also made along selected lidar orbits to verify the characteristic anticyclonic rotation of the dust plume over the eastern Atlantic as well as to trace the origin of a dust outbreak over West Africa. A detailed synoptic analysis including the satellite-derived optical depths, vertical lidar backscattering cross section profiles, and back trajectories of the 16–19 September 1994 Saharan dust outbreak over the easte...

Bounding the role of black carbon in the climate system: A scientific assessment

Abstract: Black carbon aerosol plays a unique and important role in Earth's climate system. Black carbon is a type of carbonaceous material with a unique combination of physical properties. This assessment provides an evaluation of black-carbon climate forcing that is comprehensive in its inclusion of all known and relevant processes and that is quantitative in providing best estimates and uncertainties of the main forcing terms: direct solar absorption; influence on liquid, mixed phase, and ice clouds; and deposition on snow and ice. These effects are calculated with climate models, but when possible, they are evaluated with both microphysical measurements and field observations. Predominant sources are combustion related, namely, fossil fuels for transportation, solid fuels for industrial and residential uses, and open burning of biomass. Total global emissions of black carbon using bottom-up inventory methods are 7500 Gg yr−1 in the year 2000 with an uncertainty range of 2000 to 29000. However, global atmospheric absorption attributable to black carbon is too low in many models and should be increased by a factor of almost 3. After this scaling, the best estimate for the industrial-era (1750 to 2005) direct radiative forcing of atmospheric black carbon is +0.71 W m−2 with 90% uncertainty bounds of (+0.08, +1.27) W m−2. Total direct forcing by all black carbon sources, without subtracting the preindustrial background, is estimated as +0.88 (+0.17, +1.48) W m−2. Direct radiative forcing alone does not capture important rapid adjustment mechanisms. A framework is described and used for quantifying climate forcings, including rapid adjustments. The best estimate of industrial-era climate forcing of black carbon through all forcing mechanisms, including clouds and cryosphere forcing, is +1.1 W m−2 with 90% uncertainty bounds of +0.17 to +2.1 W m−2. Thus, there is a very high probability that black carbon emissions, independent of co-emitted species, have a positive forcing and warm the climate. We estimate that black carbon, with a total climate forcing of +1.1 W m−2, is the second most important human emission in terms of its climate forcing in the present-day atmosphere; only carbon dioxide is estimated to have a greater forcing. Sources that emit black carbon also emit other short-lived species that may either cool or warm climate. Climate forcings from co-emitted species are estimated and used in the framework described herein. When the principal effects of short-lived co-emissions, including cooling agents such as sulfur dioxide, are included in net forcing, energy-related sources (fossil fuel and biofuel) have an industrial-era climate forcing of +0.22 (−0.50 to +1.08) W m−2 during the first year after emission. For a few of these sources, such as diesel engines and possibly residential biofuels, warming is strong enough that eliminating all short-lived emissions from these sources would reduce net climate forcing (i.e., produce cooling). When open burning emissions, which emit high levels of organic matter, are included in the total, the best estimate of net industrial-era climate forcing by all short-lived species from black-carbon-rich sources becomes slightly negative (−0.06 W m−2 with 90% uncertainty bounds of −1.45 to +1.29 W m−2). The uncertainties in net climate forcing from black-carbon-rich sources are substantial, largely due to lack of knowledge about cloud interactions with both black carbon and co-emitted organic carbon. In prioritizing potential black-carbon mitigation actions, non-science factors, such as technical feasibility, costs, policy design, and implementation feasibility play important roles. The major sources of black carbon are presently in different stages with regard to the feasibility for near-term mitigation. This assessment, by evaluating the large number and complexity of the associated physical and radiative processes in black-carbon climate forcing, sets a baseline from which to improve future climate forcing estimates.

The Environmental Protection Agency

Abstract: The Environmental Protection Agency (EPA) provides access to information on a variety of topics related to the environment and strives to inform citizens of health risks. The EPA also has an extensive library network that consists of 26 libraries throughout the United States, which provide access to a plethora of information to EPA employees, scientists, and researchers. The EPA implemented a reorganization project to digitize their materials so they would be more accessible to a wider range of users, but this plan was drastically accelerated when the EPA was threatened with a budget cut. It chose to close and reduce the hours and services of some of their libraries. As a result, the agency was accused of denying users the “right to know” by making information unavailable, not providing an adequate strategic plan, and discarding vital materials. This case study explores the background of the digitization project, the practices implemented, and the critiques of the project.

Sources and distributions of dust aerosols simulated with the GOCART model

Abstract: The global distribution of dust aerosol is simulated with the Georgia Tech/Goddard Global Ozone Chemistry Aerosol Radiation and Transport (GOCART) model. In this model all topographic lows with bare ground surface are assumed to have accumulated sediments which are potential dust sources. The uplifting of dust particles is expressed as a function of surface wind speed and wetness. The GOCART model is driven by the assimilated meteorological fields from the Goddard Earth Observing System Data Assimilation System (GEOS DAS) which facilitates direct comparison with observations. The model includes seven size classes of mineral dust ranging from 0.1–6 μm radius. The total annual emission is estimated to be between 1604 and 1960 Tg yr−1 in a 5-year simulation. The model has been evaluated by comparing simulation results with ground-based measurements and satellite data. The evaluation has been performed by comparing surface concentrations, vertical distributions, deposition rates, optical thickness, and size distributions. The comparisons show that the model results generally agree with the observations without the necessity of invoking any contribution from anthropogenic disturbances to soils. However, the model overpredicts the transport of dust from the Asian sources to the North Pacific. This discrepancy is attributed to an overestimate of small particle emission from the Asian sources.

The atmospheric input of trace species to the world ocean

Abstract: Over the past decade it has become apparent that the atmosphere is a significant pathway for the transport of many natural and pollutant materials from the continents to the ocean. The atmospheric input of many of these species can have an impact (either positive or negative) on biological processes in the sea and on marine chemical cycling. For example, there is now evidence that the atmosphere may be an important transport path for such essential nutrients as iron and nitrogen in some regions. In this report we assess current data in this area, develop global scale estimates of the atmospheric fluxes of trace elements, mineral aerosol, nitrogen species, and synthetic organic compounds to the ocean; and compare the atmospheric input rates of these substances to their input via rivers. Trace elements considered were Pb, Cd, Zn, Cu, Ni, As, Hg, Sn, Al, Fe, Si, and P. Oxidized and reduced forms of nitrogen were considered, including nitrate and ammonium ions and the gaseous species NO, NO2, HNO3, and NH3. Synthetic organic compounds considered included polychlorinated biphenyls (PCBs), hexachlorocyclohexanes (HCHs), DDTs, chlordane, dieldrin, and hexachlorobenzenes (HCBs). Making this assessment was difficult because there are very few actual measurements of deposition rates of these substances to the ocean. However, there are considerably more data on the atmospheric concentrations of these species in aerosol and gaseous form. Mean concentration data for 10° × 10° ocean areas were determined from the available concentration data or from extrapolation of these data into other regions. These concentration distributions were then combined with appropriate exchange coefficients and precipitation fields to obtain the global wet and dry deposition fluxes. Careful consideration was given to atmospheric transport processes as well as to removal mechanisms and the physical and physicochemical properties of aerosols and gases. Only annual values were calculated. On a global scale atmospheric inputs are generally equal to or greater than riverine inputs, and for most species atmospheric input to the ocean is significantly greater in the northern hemisphere than in the southern hemisphere. For dissolved trace metals in seawater, global atmospheric input dominates riverine input for Pb, Cd, and Zn, and the two transport paths are roughly equal for Cu, Ni, As, and Fe. Fluxes and basin-wide deposition of trace metals are generally a factor of 5-10 higher in the North Atlantic and North Pacific regions than in the South Atlantic and South Pacific. Global input of oxidized and reduced nitrogen species are roughly equal to each other, although the major fraction of oxidized nitrogen enters the ocean in the northern hemisphere, primarily as a result of pollution sources. Reduced nitrogen species are much more uniformly distributed, suggesting that the ocean itself may be a significant source. The global atmospheric input of such synthetic organic species as HCH,PCBs, DDT, and HCB completely dominates their input via rivers.

The Collection 6 MODIS aerosol products over land and ocean

Abstract: . The twin Moderate resolution Imaging Spectroradiometer (MODIS) sensors have been flying on Terra since 2000 and Aqua since 2002, creating an extensive data set of global Earth observations. Here, we introduce the Collection 6 (C6) algorithm to retrieve aerosol optical depth (AOD) and aerosol size parameters from MODIS-observed spectral reflectance. While not a major overhaul from the previous Collection 5 (C5) version, there are enough changes that there are significant impacts to the products and their interpretation. The C6 aerosol data set will be created from three separate retrieval algorithms that operate over different surface types. These are the two "Dark Target" (DT) algorithms for retrieving (1) over ocean (dark in visible and longer wavelengths) and (2) over vegetated/dark-soiled land (dark in the visible), plus the "Deep Blue" (DB) algorithm developed originally for retrieving (3) over desert/arid land (bright in the visible). Here, we focus on DT-ocean and DT-land (#1 and #2). We have updated assumptions for central wavelengths, Rayleigh optical depths and gas (H2O, O3, CO2, etc.) absorption corrections, while relaxing the solar zenith angle limit (up to ≤ 84°) to increase poleward coverage. For DT-land, we have updated the cloud mask to allow heavy smoke retrievals, fine-tuned the assignments for aerosol type as function of season/location, corrected bugs in the Quality Assurance (QA) logic, and added diagnostic parameters such topographic altitude. For DT-ocean, improvements include a revised cloud mask for thin-cirrus detection, inclusion of wind speed dependence on the surface reflectance, updates to logic of QA Confidence flag (QAC) assignment, and additions of important diagnostic information. At the same time, we quantified how "upstream" changes to instrument calibration, land/sea masking and cloud masking will also impact the statistics of global AOD, and affect Terra and Aqua differently. For Aqua, all changes will result in reduced global AOD (by 0.02) over ocean and increased AOD (by 0.02) over land, along with changes in spatial coverage. We compared preliminary data to surface-based sun photometer data, and show that C6 should improve upon C5. C6 will include a merged DT/DB product over semi-arid land surfaces for reduced-gap coverage and better visualization, and new information about clouds in the aerosol field. Responding to the needs of the air quality community, in addition to the standard 10 km product, C6 will include a global (DT-land and DT-ocean) aerosol product at 3 km resolution.