Symmetric patterns are more appealing to human observers than asymmetric ones. Here, we investigate the visual information processing mechanisms underlying this aesthetic preference. All stimuli were derived from phase scrambled versions of forty face or nature images. In addition to the scrambled images, there were four other types of test image: symmetric, in which one part of the image was a reflection of another around an axis; repetitive, in which one part of the image was a copy of the other; anti-symmetric, similar to symmetric but with the contrast of one side reversed; and interleaved patterns, in which half of the symmetric pattern was replaced by a scrambled image. The number of axes ranged from 1 to 16 for all image types. The task of our 20 observers was to give a preference rating to each image on a 6-point Lickert scale. The preference rating increased with the number of axes for all stimulus types. The observers showed a similar preference for symmetric and repetitive patterns and slightly less preference for anti-symmetric patterns. The preference for interleaved patterns was much less than for other types of stimuli. Preference for an image cannot be explained by either the ecological significance of its content or the slope of its amplitude spectrum. Instead, preference can be accounted for by the complexity of the image.
Following single-photon dissociation of CH(2)I(2) at 248 nm, I(2) molecular elimination is detected by using cavity ring-down absorption spectroscopy. The technique comprises two laser beams propagating in a perpendicular configuration, in which a tunable laser beam along the axis of the ring-down cell probes the I(2) fragment in the B (3)Π(ou)(+) - X (1)Σ(g)(+) transition. The nascent vibrational populations for v = 0, 1, and 2 levels are obtained with a population ratio of 1:(0.65 ± 0.10):(0.30 ± 0.05), corresponding to a Boltzmann-like vibrational temperature of 544 ± 73 K. The quantum yield of the ground state I(2) elimination reaction is determined to be 0.0040 ± 0.0025. With the aid of ab initio potential energy calculations, the pathway of molecular elimination is proposed on the energetic ground state CH(2)I(2) via internal conversion, followed by asynchronous three-center dissociation. A positive temperature effect supports the proposed mechanism.
A primary dissociation channel of Br(2) elimination is detected following a single-photon absorption of (COBr)(2) at 248 nm by using cavity ring-down absorption spectroscopy. The technique contains two laser beams propagating in a perpendicular configuration. The tunable laser beam along the axis of the ring-down cell probes the Br(2) fragment in the B(3)Π(ou)(+)-X(1)Σ(g)(+) transition. The measurements of laser energy- and pressure-dependence and addition of a Br scavenger are further carried out to rule out the probability of Br(2) contribution from a secondary reaction. By means of spectral simulation, the ratio of nascent vibrational population for v = 0, 1, and 2 levels is evaluated to be 1:(0.65 ± 0.09):(0.34 ± 0.07), corresponding to a Boltzmann vibrational temperature of 893 ± 31 K. The quantum yield of the ground state Br(2) elimination reaction is determined to be 0.11 ± 0.06. With the aid of ab initio potential energy calculations, the pathway of molecular elimination is proposed on the energetic ground state (COBr)(2) via internal conversion. A four-center dissociation mechanism is followed synchronously or sequentially yielding three fragments of Br(2) + 2CO. The resulting Br(2) is anticipated to be vibrationally hot. The measurement of a positive temperature effect supports the proposed mechanism.
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