Light splitting in nanoporous gold and silver

Figure Persented: Nanoporous gold and silver exhibit strong, omnidirectional broad-band absorption in the far-field. Even though they consist entirely of gold or silver atoms, these materials appear black and dull, in great contrast with the familiar luster of continuous gold and silver. The nature of these anomalous optical characteristics is revealed here by combining nanoscale electron energy loss spectroscopy with discrete dipole and boundary element simulations. It is established that the strong broad-band absorption finds its origin in nanoscale splitting of light, with great local variations in the absorbed color. This nanoscale polychromaticity results from the excitation of localized surface plasmon resonances, which are imaged and analyzed here with deep sub-wavelength, nanometer spatial resolution. We demonstrate that, with this insight, it is possible to customize the absorbance and reflectance wavelength bands of thin nanoporous films by only tuning their morphology. © 2011 American Chemical Society

Ecomorphological diversity of Australian tadpoles

Ecomorphology is the association between an organism’s morphology and its ecology. Larval anuran amphibians (tadpoles) are classified into distinct ecomorphological guilds based upon morphological features and observations of their ecology. The extent to which guilds comprise distinct morphologies resulting from convergent evolution, the degree of morphological variability within each guild, and the degree of continuity in shape between guilds has not previously been examined in a phylogenetically-informed statistical framework. Here we examine tadpole ecomorphological guilds at a macroevolutionary scale by examining morphological diversity across the Australian continent. We use ecological data to classify species to guilds, and geometric morphometrics to quantify body shape in the tadpoles of 188 species, 77% of Australian frog diversity. We find that the ecomorphological guilds represented by Australian species are morphologically distinct, but there is substantial morphological variation associated with each guild, and all guilds together form a morphological continuum. However in a phylogenetic comparative context there is no significant difference in body shape among guilds. We also relate the morphological diversity of the Australian assemblage of tadpoles to a global sample and demonstrate that ecomorphological diversity of Australian tadpoles is limited with respect to worldwide species. Our results demonstrate that general patterns of ecomorphological variation are upheld in Australian tadpoles, but tadpole body shape is more variable and possibly generalist than generally appreciated.Emma Sherratt, Marion Anstis, J. Scott Keog

Local biases drive, but do not determine, the perception of illusory trajectories

When a dot moves horizontally across a set of tilted lines of alternating orientations, the dot appears to be moving up and down along its trajectory. This perceptual phenomenon, known as the slalom illusion, reveals a mismatch between the veridical motion signals and the subjective percept of the motion trajectory, which has not been comprehensively explained. In the present study, we investigated the empirical boundaries of the slalom illusion using psychophysical methods. The phenomenon was found to occur both under conditions of smooth pursuit eye movements and constant fixation, and to be consistently amplified by intermittently occluding the dot trajectory. When the motion direction of the dot was not constant, however, the stimulus display did not elicit the expected illusory percept. These findings confirm that a local bias towards perpendicularity at the intersection points between the dot trajectory and the tilted lines cause the illusion, but also highlight that higher-level cortical processes are involved in interpreting and amplifying the biased local motion signals into a global illusion of trajectory perception

Local biases drive, but do not determine, the perception of illusory trajectories

When a dot moves horizontally across a set of tilted lines of alternating orientations, the dot appears to be moving up and down along its trajectory. This perceptual phenomenon, known as the slalom illusion, reveals a mismatch between the veridical motion signals and the subjective percept of the motion trajectory, which has not been comprehensively explained. In the present study, we investigated the empirical boundaries of the slalom illusion using psychophysical methods. The phenomenon was found to occur both under conditions of smooth pursuit eye movements and constant fixation, and to be consistently amplified by intermittently occluding the dot trajectory. When the motion direction of the dot was not constant, however, the stimulus display did not elicit the expected illusory percept. These findings confirm that a local bias towards perpendicularity at the intersection points between the dot trajectory and the tilted lines cause the illusion, but also highlight that higher-level cortical processes are involved in interpreting and amplifying the biased local motion signals into a global illusion of trajectory perception

Adult frogs and tadpoles have different macroevolutionary patterns across the Australian continent

Published online: 14 August 2017Developmental changes through an animal’s life are generally understood to contribute to the resulting adult morphology. Possible exceptions are species with complex life cycles, where individuals pass through distinct ecological and morphological life stages during their ontogeny, ending with metamorphosis to the adult form. Antagonistic selection is expected to drive low genetic correlations between life stages, theoretically permitting stages to evolve independently. Here we describe, using Australian frog radiation, the evolutionary consequences on morphological evolution when life stages are under different selective pressures. We use morphometrics to characterize body shape of tadpoles and adults across 166 species of frog and investigate similarities in the two resulting morphological spaces (morphospaces) to test for concerted evolution across metamorphosis in trait variation during speciation. A clear pattern emerges: Australian frogs and their tadpoles are evolving independently; their markedly different morphospaces and contrasting estimated evolutionary histories of body shape diversification indicate that different processes are driving morphological diversification at each stage. Tadpole morphospace is characterized by rampant homoplasy, convergent evolution and high lineage density. By contrast, the adult morphospace shows greater phylogenetic signal, low lineage density and divergent evolution between the main clades. Our results provide insight into the macroevolutionary consequences of a biphasic life cycle.Emma Sherratt, Marta Vidal-García, Marion Anstis and J. Scott Keog

Perception of Fourier and non- Fourier motion by larval zebrafish

articles Zebrafish larvae innately begin responding to moving stimuli shortly after hatching. In their optomotor response, which is elicited by large moving stimuli presented from below or the side 1,2 , larvae swim in the direction of perceived motion. The distance they travel in a given time indicates the effectiveness of the stimulus. By observing the response of many larvae to computer-animated displays, we could determine which attributes of a moving stimulus the zebrafish visual system detects. If luminance-defined features drift smoothly or jump in space, they can produce strong sensations of motion. A number of proposed models explain how motion information can be extracted. In a simple model, a point-to-point comparison is made between the luminance pattern and a spatially displaced copy of the pattern that was seen a short time before 3 . The displacement that gives the best fit tells the brain the direction and speed of movement. A more complex strategy is to look at the Fourier motion energy in the visual scene Although there is evidence that humans can use both feature matching and motion energy to detect movement 7 , they may also sense motion when presented with stimuli in which only secondorder features such as contrast, texture or flicker are moving Here we find that the fish larvae detect moving features of visu- A moving grating elicits innate optomotor behavior in zebrafish larvae; they swim in the direction of perceived motion. We took advantage of this behavior, using computer-animated displays, to determine what attributes of motion are extracted by the fish visual system. As in humans, first-order (luminance-defined or Fourier) signals dominated motion perception in fish; edges or other features had little or no effect when presented with these signals. Humans can see complex movements that lack first-order cues, an ability that is usually ascribed to higher-level processing in the visual cortex. Here we show that second-order (non-Fourier) motion displays induced optomotor behavior in zebrafish larvae, which do not have a cortex. We suggest that second-order motion is extracted early in the lower vertebrate visual pathway. al stimuli in a way that is qualitatively similar to humans: both firstorder and second-order cues drive their behavioral response. Our demonstration of second-order motion detection in fish challenges the idea that higher-level, cortical mechanisms are necessary to explain this capacity of the visual system. RESULTS Optomotor responses to Fourier motion The assay used to measure optomotor responses is similar to the one described previously 2 (Methods). Movies showing drifting gratings evoke strong optomotor responses in almost all fish in a clutch. Fish do not respond to a moving grating with a stripe width narrower than approximately 9°, which is slightly less than the predicted resolution limit of the larval cone mosaic, 6°at this age In the following experiments, responses were normalized to the effect of a designated strong stimulus, a 100% contrast square wave subtending 100°of visual angle per cycle and moving at 1 Hz for 30 seconds Although the fish seemed to follow a motion signal in the movies, it was possible that they were tracking features such as light or dark regions or edges that were being displaced. We did an experiment to show that the optomotor response is truly a response to motion. A motion display was shown of a sine wave grating tha

A role for eyebrows in regulating the visibility of eye gaze direction

The human eye is unique amongst those of primates in having white sclera against which the dark iris is clearly visible. This high-contrast structure makes the gaze direction of a human potentially easily perceptible to others. For a social creature such as a human, the ability to perceive the direction of another’s gaze may be very useful, since gaze usually signals attention. We report data showing that the accuracy of gaze deviation detection is independent of viewing distance up to a certain critical distance, beyond which it collapses. This is, of itself, surprising since most visual tasks are performed better at closer viewing distances. Our data also show that the critical distance, but not accuracy, is affected by the position of the eyebrows so that lowering the eyebrows reduces the critical distance. These findings show that mechanisms exist by which humans could expand or restrict the availability of their gaze direction to others. A way to regulate the availability of the gaze-direction signal could be an advantage. We show that an interpretation of eyebrow function in these terms provides a novel explanation for several well-known eyebrow actions, including the eyebrow flash

Ambiguity in high definition: Gaze determines physical interpretation of ambiguous rotation even in the absence of a visual context

YesPhysical interactions between objects, or between an object and the ground, are amongst the most biologically relevant for live beings. Prior knowledge of Newtonian physics may play a role in disambiguating an object’s movement as well as foveation by increasing the spatial resolution of the visual input. Observers were shown a virtual 3D scene, representing an ambiguously rotating ball translating on the ground. The ball was perceived as rotating congruently with friction, but only when gaze was located at the point of contact. Inverting or even removing the visual context had little influence on congruent judgements compared with the effect of gaze. Counterintuitively, gaze at the point of contact determines the solution of perceptual ambiguity, but independently of visual context. We suggest this constitutes a frugal strategy, by which the brain infers dynamics locally when faced with a foveated input that is ambiguous.J.S. was funded by a College of Life Sciences studentship from the University of Leicester

A New SiC-Whisker-Reinforced Lithium Aluminosilicate Composite

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/65747/1/j.1151-2916.1993.tb04016.x.pd

Default perception of high-speed motion

When human observers are exposed to even slight motion signals followed by brief visual transients—stimuli containing no detectable coherent motion signals—they perceive large and salient illusory jumps. This novel effect, which we call “high phi”, challenges well-entrenched assumptions about the perception of motion, namely the minimal-motion principle and the breakdown of coherent motion perception with steps above an upper limit. Our experiments with transients such as texture randomization or contrast reversal show that the magnitude of the jump depends on spatial frequency and transient duration, but not on the speed of the inducing motion signals, and the direction of the jump depends on the duration of the inducer. Jump magnitude is robust across jump directions and different types of transient. In addition, when a texture is actually displaced by a large step beyond dmax, a breakdown of coherent motion perception is expected, but in the presence of an inducer observers again perceive coherent displacements at or just above dmax. In sum, across a large variety of stimuli, we find that when incoherent motion noise is preceded by a small bias, instead of perceiving little or no motion, as suggested by the minimal-motion principle, observers perceive jumps whose amplitude closely follows their own dmax limits