Airborne Aerosol in Situ Measurements during TCAP: A Closure Study of Total Scattering

We present a framework for calculating the total scattering of both non-absorbing and absorbing aerosol at ambient conditions from aircraft data. Our framework is developed emphasizing the explicit use of chemical composition data for estimating the complex refractive index (RI) of particles, and thus obtaining improved ambient size spectra derived from Optical Particle Counter (OPC) measurements. The feasibility of our framework for improved calculations of total scattering is demonstrated using three types of data collected by the U.S. Department of Energy’s (DOE) aircraft during the Two-Column Aerosol Project (TCAP). Namely, these data types are: (1) size distributions measured by a suite of OPC’s; (2) chemical composition data measured by an Aerosol Mass Spectrometer and a Single Particle Soot Photometer; and (3) the dry total scattering coefficient measured by a integrating nephelometer and scattering enhancement factor measured with a humidification system. We demonstrate that good agreement (~10%) between the observed and calculated scattering can be obtained under ambient conditions (RH < 80%) by applying chemical composition data for the RI-based correction of the OPC-derived size spectra. We also demonstrate that ignoring the RI-based correction or using non-representative RI values can cause a substantial underestimation (~40%) or overestimation (~35%) of the calculated scattering, respectively

Information content analysis for a novel TES-based hyperspectral microwave atmospheric sounding instrument

In context of numerical weather prediction (NWP), increased usage of satellites radiance observations from passive microwave sensors have brought significant improvements in the forecast skills. In the infrared spectral region, hyperspectral sounder instruments such as IASI have already benefitted the NWP assimilation systems, but they are useful only under clear sky conditions. Currently, microwave instruments are providing wealth of information on clouds, precipitation and surface etc., but only with limited number of channels. Furthermore, due to limited number of channels and with poor signal-to-noise ratio, existing passive microwave sensors have very poor resolution and accuracy. We are currently developing a new microwave instrument concept, based on superconducting filterbank spectrometers, which will enable high spectral resolution observations of atmospheric temperature and humidity profiles across the microwave/sub-millimeter wavelength region with photon-noise-limited sensitivity. This study aims at investigating the information content on temperature and water-vapour that could be provided by such a hyperspectral microwave instrument under clear sky-conditions. Here, we present a new concept of Transition Edge Sensors (TESs)-based hyperspectral microwave instrument for atmospheric sounding applications. In this study, for assessing the impact of hyperspectral sampling in microwave spectral region in clear sky-conditions, we have estimated the information content as standard figure of merit called as degrees of freedom for signal (DFS). The DFS for a set of temperature and humidity sounding channels (50-60 GHz, 118GHz and 183 GHz) have been analyzed under the linear optimal estimation theory framework

A Closure Study of Total Scattering Using Airborne In Situ Measurements from the Winter Phase of TCAP

We examine the performance of our approach for calculating the total scattering coefficient of both non-absorbing and absorbing aerosol at ambient conditions from aircraft data. Our extended examination involves airborne in situ data collected by the U.S. Department of Energy's (DOE) Gulf Stream 1 aircraft during winter over Cape Cod and the western North Atlantic Ocean as part of the Two-Column Aerosol Project (TCAP). The particle population represented by the winter dataset, in contrast with its summer counterpart, contains more hygroscopic particles and particles with an enhanced ability to absorb sunlight due to the larger fraction of black carbon. Moreover, the winter observations are characterized by more frequent clouds and a larger fraction of super-micron particles. We calculate model total scattering coefficient at ambient conditions using size spectra measured by optical particle counters (OPCs) and ambient complex refractive index (RI) estimated from measured chemical composition and relative humidity (RH). We demonstrate that reasonable agreement (similar to 20% on average) between the observed and calculated scattering can be obtained under subsaturated ambient conditions (RH < 80%) by applying both screening for clouds and chemical composition data for the RI-based correction of the OPC-derived size spectra

Overview of the 2010 Carbonaceous Aerosols and Radiative Effects Study (CARES)

Substantial uncertainties still exist in the scientific understanding of the possible interactions between urban and natural (biogenic) emissions in the production and transformation of atmospheric aerosol and the resulting impact on climate change. The US Department of Energy (DOE) Atmospheric Radiation Measurement (ARM) program’s Carbonaceous Aerosol and Radiative Effects Study (CARES) carried out in June 2010 in Central Valley, California, was a comprehensive effort designed to improve this understanding. The primary objective of the field study was to investigate the evolution of secondary organic and black carbon aerosols and their climate-related properties in the Sacramento urban plume as it was routinely transported into the forested Sierra Nevada foothills area. Urban aerosols and trace gases experienced significant physical and chemical transformations as they mixed with the reactive biogenic hydrocarbons emitted from the forest. Two heavily-instrumented ground sites – one within the Sacramento urban area and another about 40 km to the northeast in the foothills area – were set up to characterize the evolution of meteorological variables, trace gases, aerosol precursors, aerosol size, composition, and climate related properties in freshly polluted and “aged” urban air. On selected days, the DOE G-1 aircraft was deployed to make similar measurements upwind and across the evolving Sacramento plume in the morning and again in the afternoon. The NASA B-200 aircraft, carrying remote sensing instruments, was also deployed to characterize the vertical and horizontal distribution of aerosols and aerosol optical properties within and around the plume. This overview provides: (a) the scientific background and motivation for the study, (b) the operational and logistical information pertinent to the execution of the study, (c) an overview of key observations and initial findings from the aircraft and ground-based sampling platforms, and (d) a roadmap of planned data analyses and focused modeling efforts that will facilitate the integration of new knowledge into improved representations of key aerosol processes and properties in climate models

The Two-Column Aerosol Project: Phase I-Overview and impact of elevated aerosol layers on aerosol optical depth

The Two-Column Aerosol Project (TCAP), conducted from June 2012 through June 2013, was a unique study designed to provide a comprehensive data set that can be used to investigate a number of important climate science questions, including those related to aerosol mixing state and aerosol radiative forcing. The study was designed to sample the atmosphere between and within two atmospheric columnsone fixed near the coast of North America (over Cape Cod, MA) and a second moveable column over the Atlantic Ocean several hundred kilometers from the coast. The U.S. Department of Energy's (DOE) Atmospheric Radiation Measurement (ARM) Mobile Facility (AMF) was deployed at the base of the Cape Cod column, and the ARM Aerial Facility was utilized for the summer and winter intensive observation periods. One important finding from TCAP is that four of six nearly cloud-free flight days had aerosol layers aloft in both the Cape Cod and maritime columns that were detected using the nadir pointing second-generation NASA high-spectral resolution lidar (HSRL-2). These layers contributed up to 60% of the total observed aerosol optical depth (AOD). Many of these layers were also intercepted by the aircraft configured for in situ sampling, and the aerosol in the layers was found to have increased amounts of biomass burning material and nitrate compared to aerosol found near the surface. In addition, while there was a great deal of spatial and day-to-day variability in the aerosol chemical composition and optical properties, no systematic differences between the two columns were observed

The Two-Column Aerosol Project: Phase I - Overview and Impact of Elevated Aerosol Layers on Aerosol Optical Depth

The Two-Column Aerosol Project (TCAP), conducted from June 2012 through June 2013, was a unique study designed to provide a comprehensive data set that can be used to investigate a number of important climate science questions, including those related to aerosol mixing state and aerosol radiative forcing. The study was designed to sample the atmosphere be tween and within two atmospheric columns; one fixed near the coast of North America (over Cape Cod, MA) and a second moveable column over the Atlantic Ocean several hundred kilometers from the coast. The U.S. Department of Energy (DOE) Atmospheric Radiation Measurement (ARM) Mobile Facility (AMF) was deployed at the base of the Cape Cod column, and the ARM Aerial Facility was utilized for the summer and winter intensive observation periods. One important finding from TCAP is that four of six nearly cloud-free flight days had aerosol layers aloft in both the Cape Cod and maritime columns that were detected using the nadir pointing second-generation NASA high-spectral resolution lidar (HSRL-2).These layer s contributed up to 60 of the total observed aerosol optical depth (AOD). Many of these layers were also intercepted by the aircraft configured for in situ sampling, and the aerosol in the layers was found to have increased amounts of biomass burning material and nitrate compared to aerosol found near the surface. In addition, while there was a great deal of spatial and day-to-day variability in the aerosol chemical composition and optical properties, no systematic differences between the two columns were observed