Results: In general, between 2006 and 2010, the discrete choice e

Results: In general, between 2006 and 2010, the discrete choice experiment indicated

that the smoking continuation rate decreased for highly dependent smokers and increased for low and moderately dependent smokers. Regarding individual measures, increases in tobacco price consistently persuaded smokers of all dependence levels to attempt to quit smoking, whereas factors such as risk information and a smoking ban were effective only for low-dependence smokers. Current smokers show less support for a price increase and legislation of health promotion than nonsmokers. Of current smokers, those with greater nicotine dependence support these policies less. Conclusions: The shift of preference for intended attempts to quit is diverse according to nicotine dependence. These differences may be derived from the variations of their time and risk preference and their trust in the tobacco price policies.”
“The link between adaptation

Crenolanib and evolutionary change remains the most central and least understood evolutionary problem. Rapid evolution and diversification of avian beaks is a textbook example of such a link, yet the mechanisms that enable beak’s precise adaptation and extensive adaptability MI-503 mouse are poorly understood. Often observed rapid evolutionary change in beaks is particularly puzzling in light of the neo-Darwinian model that necessitates coordinated changes in developmentally distinct precursors and correspondence between functional and genetic modularity, which should preclude evolutionary diversification. I show that during first 19 generations after colonization of a novel environment, house finches (Carpodacus mexicanus) express an array of distinct, but adaptively equivalent beak morphologies-a result of compensatory developmental interactions between beak length and width in accommodating

microevolutionary change in beak depth. Directional selection was largely confined to the elimination of extremes formed by these developmental interactions, while long-term stabilizing selection along a single axis-beak depth-was mirrored in the structure of beak’s additive genetic covariance. These results emphasize three principal points. click here First, additive genetic covariance structure may represent a historical record of the most recurrent developmental and functional interactions. Second, adaptive equivalence of beak configurations shields genetic and developmental variation in individual components from depletion by natural selection. Third, compensatory developmental interactions among beak components can generate rapid reorganization of beak morphology under novel conditions and thus greatly facilitate both the evolution of precise adaptation and extensive diversification, thereby linking adaptation and adaptability in this classic example of Darwinian evolution.

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