Formation of ozone and growth of aerosols in young smoke plumes from biomass burning: 1. Lagrangian parcel studies

We have developed a new model of the gas- and aerosol-phase chemistry of biomass burning smoke plumes called Aerosol Simulation Program (ASP). Here we use ASP combined with a Lagrangian parcel model to simulate the chemistry in smoke plumes from three fires: the Otavi savannah fire in Namibia, an Alaska boreal forest fire, and the Timbavati savannah fire. Our model explained the observations of ozone in the Otavi and Alaska plumes fairly well, but our initial model simulation of the Timbavati plume underestimated the concentrations of ozone, OH, and secondary aerosol matter. The Timbavati simulation agrees with observations if we increase OH to equal its observed levels. Heterogeneous reactions of NO2 and SO2 could explain the needed higher concentrations of OH and the rapid formation of ozone, nitrate, and sulfate in the smoke plume if the uptake coefficients on smoke aerosols are large (O(10−3) and O(10−4), respectively). Uncharacterized organic species in the smoke plume were likely responsible for the rapid formation of aerosol organic carbon. The changes in the aerosol size distribution were dominated by plume dilution and condensational growth. The single scattering albedo of the modeled smoke increases from 0.866 to 0.902 over 1 h of aging. The change in aerosol scattering with relative humidity for the modeled fresh smoke matches observations up to 66% RH, but the model greatly overestimates the humidification factor at 80% RH (2.88 versus an observed value of 1.70–1.79). For the aged smoke, the modeled humidification factor is 1.22, slightly below the observed value of 1.40.National Science Foundation (U.S.)Massachusetts Institute of Technology. Presidential FellowshipNational Science Foundation (U.S.) (NSF grant ATM- 0120468)United States. Dept. of Energy (DOE grant DE-FG-R61937)Martin Family Society of Fellows for SustainabilityMassachusetts Institute of Technology. Joint Program on the Science and Policy of Global Chang

ICE IN THE 1994 RABAUL ERUPTION CLOUD - IMPLICATIONS FOR VOLCANO HAZARD AND ATMOSPHERIC EFFECTS

VOLCANIC clouds are an important natural hazard to aircraft1, and host chemical reactions that interest both volcanologists2,3 and atmospheric scientists4-6. Ice has been suggested as a possible component of eruption clouds7, but there has been no direct evidence for its presence. Here we report the detection, using a satellite-borne infrared sensor, of ≳ 2 million tonnes of ice in the cloud produced by the September 1994 eruption of Rabaul volcano, in Papua New Guinea. The cloud also contained relatively low levels of sulphur dioxide (80 ± 50 kilotonnes), compared with other stratospheric eruption clouds. The unusual aspects of this cloud may be related to the entry of sea water into the volcanic vent, and its participation in the eruption column. Past eruptions that occurred in similar (coastal) settings, such as those of Krakatau and Santorini, might have had less effect on the atmosphere than their volume alone would suggest, because the presence of ice may decrease the residence time of ash and sulphur in the atmosphere. In addition, the ability of ice to mask the characteristic spectral signature of volcanic ash will increase the difficulty of designing airborne ash detection systems for aviation safety

Atmospheric composition change: global and regional air quality

Air quality transcends all scales with in the atmosphere from the local to the global with handovers and feedbacks at each scale interaction. Air quality has manifold effects on health, ecosystems, heritage and climate. In this review the state of scientific understanding in relation to global and regional air quality is outlined. The review discusses air quality, in terms of emissions, processing and transport of trace gases and aerosols. New insights into the characterization of both natural and anthropogenic emissions are reviewed looking at both natural (e.g. dust and lightning) as well as plant emissions. Trends in anthropogenic emissions both by region and globally are discussed as well as biomass burning emissions. In terms of chemical processing the major air quality elements of ozone, non-methane hydrocarbons, nitrogen oxides and aerosols are covered. A number of topics are presented as a way of integrating the process view into the atmospheric context; these include the atmospheric oxidation efficiency, halogen and HOx chemistry, nighttime chemistry, tropical chemistry, heat waves, megacities, biomass burning and the regional hot spot of the Mediterranean. New findings with respect to the transport of pollutants across the scales are discussed, in particular the move to quantify the impact of long-range transport on regional air quality. Gaps and research questions that remain intractable are identified. The review concludes with a focus of research and policy questions for the coming decade. In particular, the policy challenges for concerted air quality and climate change policy (co-benefit) are discussed