Atmospheric Chemistry and Physics (ACP) is an international scientific journal dedicated to the publication and public discussion of high-quality studies investigating the Earth's atmosphere and the underlying chemical and physical processes. It covers the altitude range from the land and ocean surface up to the turbopause, including the troposphere, stratosphere, and mesosphere.
The main subject areas comprise atmospheric modelling, field measurements, remote sensing, and laboratory studies of gases, aerosols, clouds and precipitation, isotopes, radiation, dynamics, biosphere interactions, and hydrosphere interactions (for details see journal subject areas). The journal scope is focused on studies with general implications for atmospheric science rather than investigations that are primarily of local or technical interest.
We show that atmospheric load of ice nuclei is enhanced for up to 20 days after key rainfall events. The rate of enhancement decreases exponentially with time. Rainfall quantity and frequency are increased for a similar duration and with similar exponential decreases thereby supporting the notion of rainfall feedback. We reveal series of significant feedback in rainfall patterns across Australia over the past century and marked changes in feedback patterns, and we indicate their locations.
E. K. Bigg, S. Soubeyrand, and C. E. Morris
This work represents the first application of two-dimensional gas chromatography to broadly characterize the gas-phase emissions of biomass burning, including comparisons among the emissions from burns of selected conifer, grass, crop residue, and peat fuel types. In these smoke samples, over 700 compounds were detected, which are discussed in the context of potential secondary organic aerosol formation.
L. E. Hatch, W. Luo, J. F. Pankow, R. J. Yokelson, C. E. Stockwell, and K. C. Barsanti
This paper describes a new ensemble methodology for the statistical analysis of atmospheric gas- & particle-phase composition data sets. The methodology reduces the huge amount of data derived from many chamber experiments to show that organic reactivity & resultant particle formation can be mapped into unique clusters in statistical space. The model generated is used to map more realistic plant mesocosm oxidation data, the projection of which gives insight into reactive pathways & precursors.
K. P. Wyche, P. S. Monks, K. L. Smallbone, J. F. Hamilton, M. R. Alfarra, A. R. Rickard, G. B. McFiggans, M. E. Jenkin, W. J. Bloss, A. C. Ryan, C. N Hewitt, and A. R MacKenzie
Glyoxal and methylglyoxal are short-lived organic trace gases and important precursors of secondary organic aerosol. Measurements over oceans are sparse. We present the first in situ glyoxal and methylglyoxal observations over remote temperate oceans, alongside observations of precursor gases. Precursor gases cannot explain observed mixing ratios, highlighting an unknown source. We show a large discrepancy between calculated vertical column densities of glyoxal and those retrieved by satellite.
S. J. Lawson, P. W. Selleck, I. E. Galbally, M. D. Keywood, M. J. Harvey, C. Lerot, D. Helmig, and Z. Ristovski
Ozone holds a certain fascination in atmospheric science. It is ubiquitous in the atmosphere, central to tropospheric oxidation chemistry, yet harmful to human and ecosystem health as well as being an important greenhouse gas. It is not emitted into the atmosphere but is a by-product of the very oxidation chemistry it largely initiates. This review examines current understanding of the processes regulating tropospheric ozone at global to local scales from both measurements and models.
P. S. Monks, A. T. Archibald, A. Colette, O. Cooper, M. Coyle, R. Derwent, D. Fowler, C. Granier, K. S. Law, D. S. Stevenson, O. Tarasova, V. Thouret, E. von Schneidemesser, R. Sommariva, O. Wild, and M. L. Williams