Abstract. Size-resolved measurements of atmospheric aerosol and cloud condensation nuclei (CCN) concentrations and hygroscopicity were conducted over a full seasonal cycle at the remote Amazon Tall Tower Observatory (ATTO, March 2014–February 2015). In a preceding companion paper, we presented annually and seasonally averaged data and parametrizations (Part 1; Pöhlker et al., 2016a). In the present study (Part 2), we analyze key features and implications of aerosol and CCN properties for the following characteristic atmospheric conditions: Empirically pristine rain forest (PR) conditions, where no influence of pollution was detectable, as observed during parts of the wet season from March to May. The PR episodes are characterized by a bimodal aerosol size distribution (strong Aitken mode with DAit ≈ 70nm and NAit ≈ 160cm−3, weak accumulation mode with Dacc ≈ 160nm and Nacc ≈ 90cm−3), a chemical composition dominated by organic compounds, and relatively low particle hygroscopicity ($ąppa$Ait ≈ 0.12, $p̨pa$acc ≈ 0.18). Long-range-transport (LRT) events, which frequently bring Saharan dust, African biomass smoke, and sea spray aerosols into the Amazon Basin, mostly during February to April. The LRT episodes are characterized by a dominant accumulation mode (DAit ≈ 80nm, NAit ≈ 120cm−3 vs. Dacc ≈ 180nm, Nacc ≈ 310cm−3), an increased abundance of dust and salt, and relatively high hygroscopicity ($kp̨a$Ait ≈ 0.18, $kaą$acc ≈ 0.35). The coarse mode is also significantly enhanced during these events. Biomass burning (BB) conditions characteristic for the Amazonian dry season from August to November. The BB episodes show a very strong accumulation mode (DAit ≈ 70nm, NAit ≈ 140cm−3 vs. Dacc ≈ 170nm, Nacc ≈ 3400cm−3), very high organic mass fractions ( ∼ 90%), and correspondingly low hygroscopicity ($kap$̨Ait ≈ 0.14, $kappącc ≈ 0.17). Mixed-pollution (MPOL) conditions with a superposition of African and Amazonian aerosol emissions during the dry season. During the MPOL episode presented here as a case study, we observed African aerosols with a broad monomodal distribution (D ≈ 130nm, NCN, 10 ≈ 1300cm−3), with high sulfate mass fractions (∼ 20%) from volcanic sources and correspondingly high hygroscopicity ($kappątextless 100 nm ≈ 0.14, $kappa$̨textgreater 100 nm ≈ 0.22), which were periodically mixed with fresh smoke from nearby fires (D ≈ 110nm, NCN, 10 ≈ 2800cm−3) with an organic-dominated composition and sharply decreased hygroscopicity ($kappa$ t̨extless 150 nm ≈ 0.10, $kappa$ ęxtgreater 150 nm ≈ 0.20). Insights into the aerosol mixing state are provided by particle hygroscopicity ($kappa$) dt̨ribution plots, which indicate largely internal mixing for the PR aerosols (narrow $kappa$ disįbution) and more external mixing for the BB, LRT, and MPOL aerosols (broad $kappa$ distb̨utions). The CCN spectra (CCN concentration plotted against water vapor supersaturation) obtained for the different case studies indicate distinctly different regimes of cloud formation and microphysics depending on aerosol properties and meteorological conditions. The measurement results suggest that CCN activation and droplet formation in convective clouds are mostly aerosol-limited under PR and LRT conditions and updraft-limited under BB and MPOL conditions. Normalized CCN efficiency spectra (CCN divided by aerosol number concentration plotted against water vapor supersaturation) and corresponding parameterizations (Gaussian error function fits) provide a basis for further analysis and model studies of aerosol–cloud interactions in the Amazon.