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. 2016 May 25;533(7604):521–526. doi: 10.1038/nature17953

Figure 1. Evolution of HOMs and particles during a typical run.

Figure 1

a, Evolution of selected HOM monomers (E1), dimers (E2) and peroxy radicals (RO2·) at 300 p.p.t.v. α-pinene, 33 p.p.b.v. O3, zero H2 or HONO, 38% relative humidity, 278 K and [H2SO4] < 5 × 104 cm−3 (the same run as shown in Extended Data Fig. 4). The HOMs start to appear soon after the first injection of α-pinene into the chamber at 21:22, 23 October 2013. A HOM monomer is a highly oxygenated molecule derived from α-pinene (C10H16), and a HOM dimer is a covalently bound pair of monomers. Peroxy radicals are identified by an odd H number. The HOMs are charged with an Inline graphic ion in the CI-APi-TOF mass spectrometer. The systematic scale uncertainty on the HOM concentrations is +80%/−45%. b, Evolution of the particle number concentrations measured in the PSM1.8 (red curve) and CPC2.5 (blue curve) particle counters. The high-voltage clearing field (HVCF) was switched off at 05:16, 24 October 2013, marking the transition from neutral (ion-free) to GCR conditions in the chamber. A sharp increase in the rate of particle formation is seen, due to ion-induced nucleation of pure biogenic particles. However, no change occurs in the HOM concentrations (a), because these are predominantly neutral gas-phase molecules. The dotted and dashed curves in b show the PSM1.8 and CPC2.5 distributions, respectively, simulated for this run with the AEROCLOUD kinetic model, which is used to derive the experimental nucleation rates (see Methods).

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