Based on the institutional vs the individual view of culture and the theory of individualism–collectivism in explaining the in-group–outgoup distinction that people make in different cultures, we predicted that Chinese people would make less cooperative decisions than Australians in mixed-motive business situations in which no formal or informal sanction systems were in place. We also predicted that Chinese would be less cooperative with foreigners than with fellow Chinese when they were in a foreign territory, whereas Australians would be equally cooperative with members of both groups. Data from two cross-national experiments provided general support for these predictions. Moreover, the results of Study 2 showed that the nation effects on cooperative decision-making were mediated by individual cultural orientation on vertical and horizontal individualism. The theoretical and practical implications of these findings are discussed in the context of cross-cultural business settings. Journal of International Business Studies (2005) 36, 622–636. doi:10.1057/palgrave.jibs.8400169

Severe haze pollution frequently occurred in China during winter. Mechanisms for the formation and evolution of high PM2.5 (particulate matter with aerodynamic diameter of 2.5 μm or less) episodes, however, remain poorly understood. We characterize two extreme haze episodes in the Yangtze River Delta region of China from 1 to 9 December (Episode I) and 19 to 24 December (Episode II) in 2016 using comprehensive measurements and model analyses. The aqueous sulfur dioxide (SO2) oxidation catalyzed by mineral ions and the heterogeneous uptakes of SO2, sulfuric acid (H2SO4), nitrogen dioxide (NO2), nitrogen trioxide (NO3), nitrogen pentoxide (N2O5), and nitric acid (HNO3) on mineral aerosols are included in the model to better represent the formation of sulfate‐nitrate‐ammonium. The optimized mechanisms substantially improve the simulations of PM2.5 composition, particularly for sulfate and nitrate. The two episodes show different synoptic conditions and evolution stages, with gradual PM2.5 increase under stagnant weather conditions in Episode I (Stage I: Slow Increase Stage, Stage II: Rapid Formation Stage, and Stage III: Dissipation Stage) and with explosive PM2.5 increase mostly associated with cross‐border transport from North China in Episode II (Stage I′: Clean Stage, Stage II′: Fast Transport Stage, and Stage III′: Clear Stage). The concentrations of sulfate‐nitrate‐ammonium increased evidently and became the key components of PM2.5 during haze episodes. The heterogeneous conversion from SO2 to sulfate on mineral aerosols is the main reason for sulfate increase, accounting for more than 50% of sulfate production. This study provides a better understanding of the causes for winter haze in China.

An ethanol solution containing one or two fullerene C 60 molecules was studied via molecular dynamics simulation. We found that the ethanol molecules form several solvation shells around the central fullerene molecule. Radial distribution functions (RDFs) and hydrogen-bond analyses were employed to detect the structure of the ethanol molecules in the solvation shells. The ethanol molecules in the first solvation shell tend to have their nonpolar alkyl groups exposed to the C 60 surface while the polar hydroxyl groups point outward to maintain a hydrogen-bond network with a clathrate-like structure. Such orientation of the ethanol molecules in the first solvation shell modulates the orientation of the ethanol molecules in the second solvation shell to have the hydroxyl groups pointing inward. The potential of mean force (PMF) between two C 60 molecules in ethanol solution showed that C 60 molecules tend to aggregate in the ethanol solution. There is no ethanol molecule in the intersolute area if the distance between the centers of mass of two C 60 molecules is shorter than 10.2 Å. The ethanol molecules near the intersolute area tend to have their methyl groups penetrating into the intersolute region if the distance between two C 60 molecules is short, although the hydroxyl groups have smaller volume. We analyzed the dynamic properties of the ethanol molecules in different solvation shells and found that the relaxation is much slower than that of water solution of C 60 molecules. In addition, the relaxation of the first solvation shell is slower than that in other solvation shells. The lifetime of the hydrogen-bond in the first solvation shell is also longer than that in other solvation shells while the reorientation of the hydrogen-bonded ethanol pair contributes little to break the hydrogen-bonds.