Atmospheric Sampling of Aerosols to Stratospheric Altitudes using High Altitude Balloons

Although carbon dioxide represents a long-lived atmospheric component relevant to global climate change, it is also understood that many additional contributors influence the overall climate of Earth. Among these, short-lived components are more difficult to incorporate into models due to uncertainties in the abundances of these both spatially and temporally. Possibly the most significant of these short-lived components falls under the heading of “black carbon” (BC). There are numerous overlapping definitions of BC, but it is basically carbonaceous in nature and light absorbing. Due to its potential as a climate forcer, an understanding of the BC population in the atmosphere is critical for modeling of radiative forcing. Prior measurements of atmospheric BC generally consist of airplane- and ground-based sampling, typically below 5000 m and restricted in time and space. Given that BC has a residence time on the order of days, short-term variability is easily missed. Further, since the radiative forcing is a result of BC distributed through the entire atmospheric column, aircraft sampling is by definition incomplete. We are in the process of planning a more comprehensive sampling of the atmosphere for BC using high-altitude balloons. Balloon-borne sampling is a highly reliable means to sample air through the entire troposphere and into the lower stratosphere. Our system will incorporate a balloon and a flight train of two modules. One module will house an atmospheric sampler. This sampler will be single-stage (samples all particle sizes together), and will place particles directly on an SEM sample stub for analysis. The nozzle depositing the sample will be offset from the center of the stub, placing the aerosol particles toward the edge. At various altitudes, the stub will be rotated 45 degrees, providing 6-8 sample “cuts” of particle populations through the atmospheric column. The flights will reach approximately 27 km altitude, above which the balloons burst and the modules return to the surface. The second module will contain instrumentation recording temperature, pressure, and humidity, plus a radio beacon to track the location, facilitating recovery. Another instrument we are planning is a small, lightweight optical aerosol spectrometer probe. This would provide a valuable secondary set of data to compare with the actual sampling. The aerosol particle population will be assessed using the SEM at Morehead State University. Over the next several years, sampling is planned at locations both near and far from urban areas, and at intermediate locations. Sampling will be conducted at four times during the year to assess seasonal variations and, at some sites, repeated short-term samplings (e.g., 5 flights in 10 days) will be undertaken to assess short-term variations. In addition, the SEM should permit the assessment of the ratio of BC to organic carbon (OC). Like BC, organic carbon species are produced through biomass burning, but are not as effective as light absorbers, so are not responsible for as much forcing as black carbon. The atmosphere is sampled at a known volumetric rate, resulting in a picture of the atmospheric column density for both BC and OC, information of great use in modeling of the aerosol contribution to climate change.