Rebecca Sharman

Luminance cues constrain chromatic blur discrimination in natural scene stimuli

Introducing blur into the color components of a natural scene has very little effect on its percept, whereas blur introduced into the luminance component is very noticeable. Here we quantify the dominance of luminance information in blur detection and examine a number of potential causes. We show that the interaction between chromatic and luminance information is not explained by reduced acuity or spatial resolution limitations for chromatic cues, the effective contrast of the luminance cue, or chromatic and achromatic statistical regularities in the images. Regardless of the quality of chromatic information, the visual system gives primacy to luminance signals when determining edge location. In natural viewing, luminance information appears to be specialized for detecting object boundaries while chromatic information may be used to determine surface properties.

The role of motion and number of element locations in mirror symmetry perception

The human visual system has specialised mechanisms for encoding mirror-symmetry and for detecting symmetric motion-directions for objects that loom or recede from the observers. The contribution of motion to mirror-symmetry perception has never been investigated. Here we examine symmetry detection thresholds for stationary (static and dynamic flicker) and symmetrically moving patterns (inwards, outwards, random directions) with and without positional symmetry. We also measured motion detection and direction-discrimination thresholds for horizontal (left, right) and symmetrically moving patterns with and without positional symmetry. We found that symmetry detection thresholds were (a) significantly higher for static patterns, but there was no difference between the dynamic flicker and symmetrical motion conditions, and (b) higher than motion detection and direction-discrimination thresholds for horizontal or symmetrical motion, with or without positional symmetry. In addition, symmetrical motion was as easy to detect or discriminate as horizontal motion. We conclude that whilst symmetrical motion per se does not contribute to symmetry perception, limiting the lifetime of pattern elements does improve performance by increasing the number of element-locations as elements move from one location to the next. This may be explained by a temporal integration process in which weak, noisy symmetry signals are combined to produce a stronger signal.

Visual adaptation alters the apparent speed of real-world actions

The apparent physical speed of an object in the field of view remains constant despite variations in retinal velocity due to viewing conditions (velocity constancy). For example, people and cars appear to move across the field of view at the same objective speed regardless of distance. In this study a series of experiments investigated the visual processes underpinning judgements of objective speed using an adaptation paradigm and video recordings of natural human locomotion. Viewing a video played in slow-motion for 30 seconds caused participants to perceive subsequently viewed clips played at standard speed as too fast, so playback had to be slowed down in order for it to appear natural; conversely after viewing fast-forward videos for 30 seconds, playback had to be speeded up in order to appear natural. The perceived speed of locomotion shifted towards the speed depicted in the adapting video (‘re-normalisation’). Results were qualitatively different from those obtained in previously reported studies of retinal velocity adaptation. Adapting videos that were scrambled to remove recognizable human figures or coherent motion caused significant, though smaller shifts in apparent locomotion speed, indicating that both low-level and high-level visual properties of the adapting stimulus contributed to the changes in apparent speed.

Edge enhancement improves disruptive camouflage by emphasising false edges and creating pictorial relief

Disruptive colouration is a visual camouflage composed of false edges and boundaries. Many disruptively camouflaged animals feature enhanced edges; light patches are surrounded by a lighter outline and/or a dark patches are surrounded by a darker outline. This camouflage is particularly common in amphibians, reptiles and lepidopterans. We explored the role that this pattern has in creating effective camouflage. In a visual search task utilising an ultra-large display area mimicking search tasks that might be found in nature, edge enhanced disruptive camouflage increases crypsis, even on substrates that do not provide an obvious visual match. Specifically, edge enhanced camouflage is effective on backgrounds both with and without shadows; i.e. this is not solely due to background matching of the dark edge enhancement element with the shadows. Furthermore, when the dark component of the edge enhancement is omitted the camouflage still provided better crypsis than control patterns without edge enhancement. This kind of edge enhancement improved camouflage on all background types. Lastly, we show that edge enhancement can create a perception of multiple surfaces. We conclude that edge enhancement increases the effectiveness of disruptive camouflage through mechanisms that may include the improved disruption of the object outline by implying pictorial relief.

Dissociating the effect of disruptive colouration on localisation and identification of camouflaged targets

Disruptive camouflage features contrasting areas of pigmentation across the animals’ surface that form false edges which disguise the shape of the body and impede detection. In many taxa these false edges feature local contrast enhancement or edge enhancement, light areas have lighter edges and dark areas have darker edges. This additional quality is often overlooked in existing research. Here we ask whether disruptive camouflage can have benefits above and beyond concealing location. Using a novel paradigm, we dissociate the time courses of localisation and identification of a target in a single experiment. We measured the display times required for a stimulus to be located or identified (the critical duration). Targets featured either uniform, disruptive or edge enhanced disruptive colouration. Critical durations were longer for identifying targets with edge enhanced disruptive colouration camouflage even when presented against a contrasting background, such that all target types were located equally quickly. For the first time, we establish empirically that disruptive camouflage not only conceals location, but also disguises identity. This shows that this form of camouflage can be useful even when animals are not hidden. Our findings offer insights into how edge enhanced disruptive colouration undermines visual perception by disrupting object recognition.

Cue combination of conflicting color and luminance edges

Abrupt changes in the color or luminance of a visual image potentially indicate object boundaries. Here, we consider how these cues to the visual “edge” location are combined when they conflict. We measured the extent to which localization of a compound edge can be predicted from a simple maximum likelihood estimation model using the reliability of chromatic (L−M) and luminance signals alone. Maximum likelihood estimation accurately predicted the pattern of results across a range of contrasts. Predictions consistently overestimated the relative influence of the luminance cue; although L−M is often considered a poor cue for localization, it was used more than expected. This need not indicate that the visual system is suboptimal but that its priors about which cue is more useful are not flat. This may be because, although strong changes in chromaticity typically represent object boundaries, changes in luminance can be caused by either a boundary or a shadow.

Spatiotemporal and luminance contrast properties of symmetry perception

Recent studies have shown that limiting the lifetime of pattern elements improves symmetry detection, potentially by increasing the number of element locations. Here, we investigate how spatial relocation, luminance contrast modulation and lifetime duration of elements affect symmetry perception in dynamic stimuli. Stimuli were dynamic dot-patterns containing varying amounts of symmetry about a vertical axis. Symmetrical matched-pairs were: (i) relocated to multiple successive, but random locations (i.e., multiple locations condition); (ii) relocated between the same two locations (i.e., two locations condition); (iii) not, relocated, but their luminance contrast was modulated at different temporal frequencies (i.e., one location condition), and (iv) not relocated, but a single pattern was presented at full contrast (i.e., static condition). In the dynamic conditions, we varied the elements’ lifetime duration and temporal frequency of contrast modulation. We measured symmetry detection thresholds using a two-interval forced choice procedure. Our results show improved performance for the multiple locations condition compared to two-location and static conditions, suggesting a cumulative process whereby weak symmetry information is integrated by spatiotemporal filters to increase overall symmetry signal strength. Performance also improved for the static, contrast modulated patterns, but this was explained by a reduction in perceived density. This suggests that different mechanisms mediate symmetry detection in dynamic stimuli and static contrast modulated patterns.

Temporal dynamics of mirror-symmetry perception

Recent studies have suggested that temporal dynamics rather than symmetrical motion-direction contribute to mirror-symmetry perception. Here we investigate temporal aspects of symmetry perception and implicitly, its temporal flexibility and limitations, by examining how symmetrical pattern elements are combined over time. Stimuli were dynamic dot-patterns consisting of either an on-going alternation of two images (sustained stimulus presentation) or just two images each presented once (transient stimulus presentation) containing different amounts of symmetry about the vertical axis. We varied the duration of the two images under five temporal-arrangement conditions: (a) whole patterns in which a symmetric pattern alternated with a noise pattern; (b) delayed halves—the halves of the symmetric and noise patterns were presented with temporal delay; (c) matched-pairs—two alternating images each containing equal amounts of symmetrical matched-pairs; (d) delayed matched-pairs—the same as arrangement (c), but with matched-pairs presented with delay; and (e) static—both images presented simultaneously as one. We found increased sensitivity in sustained compared to transient stimulus presentations and with synchronous compared to delayed matched-pairs stimuli. For the delayed conditions, sensitivity decreased gradually with longer image durations (>60 ms), prominently for the transient stimulus presentations. We conclude that spatial correlations across-the-symmetry-midline can be integrated over time (∼120 ms), and symmetry mechanisms can tolerate temporal delays between symmetric dot-pairs of up to ∼60 ms.

Adaptation to human locomotion speed

Visual judgments of human movement play an important role in social interactions, but relatively little is known about how retinal motion signals are used to estimate human movement speed. We report a new effect which demonstrates that these judgments are subject to modification by exposure to dynamic images. Participants viewed videos of real scenes depicting either groups of figures walking along a High Street or contestants running in the London Marathon. When video playback was speeded up or slowed down slightly relative to natural speed, participants could readily report whether the figures in each video appeared to be moving unnaturally quickly or slowly. However after adapting to slowed-down walking, natural walking speed appeared too fast, and after adapting to speeded-up walking, natural walking speed appeared too slow. Corresponding effects were found for running videos. Adaptation to natural-speed playback had no effect on apparent locomotion speed. These effects are quite different in a number of respects from those previously reported in studies of retinal velocity adaptation using simple patterns such as gratings. Unlike the stimuli used in most previous studies our videos contained a range of speeds and directions due to the unpredictability of natural scenes. Walkers and runners moved in different directions at different speeds, and at varying distances from the camera. Participants also engaged in free viewing rather than fixation. Furthermore over the range of retinal velocities our stimuli contained, adaptation to simple moving patterns causes a significant reduction in apparent velocity at all test velocities, including at the adapting velocity. Our data are consistent with the operation of a qualitatively different process in judgements of locomotion speed in natural scenes.