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Abstract: Long‐term measurements (1972–2015) of the reflectivity of Uranus at 472 and 551 nm display variability that is incompletely explained by seasonal effects. Spectral analysis shows that this nonseasonal variability tracks the 11 year solar cycle. Two mechanisms could cause solar modulation: (a) nucleation onto ions or electrons created by galactic cosmic rays (GCR) or (b) UV‐induced aerosol color changes. Ion‐aerosol theory is used to identify expected relationships between reflectivity fluctuations and GCR flux, tested with multiple regression and compared to the linear response predicted between reflectivity and solar UV flux. The statistics show that 24% of the variance in reflectivity fluctuations at 472 nm is explained by GCR ion‐induced nucleation, compared to 22% for a UV‐only mechanism. Similar GCR‐related variability exists in Neptune's atmosphere; hence, the effects found at Uranus provide the first example of common variability in two planetary atmospheres driven through energetic particle modulation by their host star. [ABSTRACT FROM AUTHOR]

Two vertical cosmic ray telescopes for atmospheric cosmic ray ionization event detection are compared. Counter A, designed for low power remote use, was deployed in the Welsh mountains; its event rate increased with altitude as expected from atmospheric cosmic ray absorption. Independently, Counter B's event rate was found to vary with incoming particle acceptance angle. Simultaneous co-located comparison of both telescopes exposed to atmospheric ionization showed a linear relationship between their event rates. [ABSTRACT FROM AUTHOR]

During a 4-week run in October-November 2006, a pilot experiment was performed at the CERN Proton Synchrotron in preparation for the Cosmics Leaving OUtdoor Droplets (CLOUD) experiment, whose aim is to study the possible influence of cosmic rays on clouds. The purpose of the pilot experiment was firstly to carry out exploratory measurements of the effect of ionising particle radiation on aerosol formation from trace H2SO4 vapour and secondly to provide technical input for the CLOUD design. A total of 44 nucleation bursts were produced and recorded, with formation rates of particles above the 3 nm detection threshold of between 0.1 and 100 cm-3 s-1, and growth rates between 2 and 37 nm h-1. The corresponding H2SO4 concentrations were typically around 106 cm-3 or less. The experimentally-measured formation rates and H2SO4 concentrations are comparable to those found in the atmosphere, supporting the idea that sulphuric acid is involved in the nucleation of atmospheric aerosols. However, sulphuric acid alone is not able to explain the observed rapid growth rates, which suggests the presence of additional trace vapours in the aerosol chamber, whose identity is unknown. By analysing the charged fraction, a few of the aerosol bursts appear to have a contribution from ion-induced nucleation and ion-ion recombination to form neutral clusters. Some indications were also found for the accelerator beam timing and intensity to influence the aerosol particle formation rate at the highest experimental SO2 concentrations of 6 ppb, although none was found at lower concentrations. Overall, the exploratory measurements provide suggestive evidence for ion-induced nucleation or ion-ion recombination as sources of aerosol particles. However in order to quantify the conditions under which ion processes become significant, improvements are needed in controlling the experimental variables and in the reproducibility of the experiments. Finally, concerning technical aspects, the most important lessons for the CLOUD design include the stringent requirement of internal cleanliness of the aerosol chamber, as well as maintenance of extremely stable temperatures (variations below 0.1 °C). [ABSTRACT FROM AUTHOR]