Testing the dorsal stream attention hypothesis: Electrophysiological correlates and the effects of ventral stream damage

The roles of dorsal and ventral processing streams in visual orienting and conscious perception were examined in two experiments. The first employed high density EEG with source localization. The second comprised a neuropsychological case study. Visual orienting was assessed with an attention procedure, where peripheral letters cued participants towards a target location. In the perception procedure participants responded to the same letters by performing an explicit conscious discrimination. In Experiment 1, the peripheral letters elicited rapid dorsal stream activation in the attention procedure, and this activation preceded top-down enhancement of target processing in occipital cortex. In the perception procedure early ventral stream activation was seen. In addition, peripheral letters elicited an “early directing attention negativity” (EDAN) over parietal recording sites in the attention procedure, but not in the perception procedure. In Experiment 2, a patient with a bilateral ventral stream lesion but preserved dorsal stream function showed clear disruption to performance in the perception procedure, whilst exhibiting a normal visual orienting effect in the attention procedure. Taken together these findings (1) highlight the distinct roles of the dorsal and ventral streams in attention and perception, and (2) suggest how these streams might interact, via reentrant effects of attention on perceptual processing.     

Dual-target search for high and low prevalence X-ray threat targets

Recent studies have shown that the prevalence of target presentation in visual search has an impact on target detection rates, and also that searching for two targets leads to a decrement in performance (the “dual-target cost”). In the present experiments, we added to previous work that has examined the interaction between the prevalence effect and dual-target cost, and also to previous work that has examined a full range of prevalence levels. We found no interaction between the dual-target cost and prevalence effect, though the response criterion in dual-target search did interact with target prevalence in an unexpected manner. Furthermore, we detected anasymmetry in the prevalence effect: It was more marked for high than low prevalence. Implications for real-world tasks are discussed.     

Incidental encoding of numerosity in visual long-term memory

The visual system can readily extract numerosity information from brief experiences. This numerical perception is characterized by diminishing accuracy as numerosity increases, and impaired discrimination for similar quantities and large magnitudes. Here we assess whether these properties apply more broadly to numerosity in visual long-term memory. In surprise memory tests, we observed: Remarkable accuracy in estimating the number of repetitions of an exemplar image (Experiment 1a), that this accuracy decreased but remained high when estimating over categories (Experiments 1b and 1c), that numerical discrimination from memory exhibited psychophysical distance and size effects (Experiment 2), that these effects may derive from stored representations rather than post hoc approximation (Experiment 3a), and that they can reflect total elapsed experience in addition to discrete counts (Experiment 3b). Similar to how numerosity is readily extracted during visual perception, our results suggest that numerosity is encoded incidentally in visual long-term memory.     

The speed of visual recognition memory

Two processes are thought to support visual recognition memory (VRM): Familiarity and recollection. The former is generally considered to be faster. However, the relationship between the precise onset of the two processes is unclear. Here, we use a novel paradigm, the SAB (Speed and Accuracy Boosting procedure) that constrains participants to use their fastest strategy and provides a continuous distribution of their reaction times. We show that fast recognition occurs as early as ~370 ms, a limit that appears incompressible whatever types of stimuli were used. In a second experiment, running the SAB in conjunction with a modified version of the remember/know paradigm, we show that responses up to ~420 ms are based solely on familiarity. These time limits of 370 ms and 420 ms provide strong constraints on the neural mechanisms underlying VRM and suggest that the fastest, familiarity-based, responses could rely on the visual ventral stream only.     

Assessing visual search performance differences between Transportation Security Administration Officers and nonprofessional visual searchers

Some visual searches depend upon accuracy (e.g., radiology, airport security screening), and it is important for both theoretical and applied reasons to understand what factors best predict performance. The current study administered a visual search task to both professional (Transportation Security Administration Officers) and nonprofessional (members of Duke University) searchers to examine group differences in which factors predict accuracy. Search speed—time taken to terminate search—was the primary predictor for nonprofessional searchers (accounting for 59% of their accuracy variability) and for the least experienced professional searchers (37% of variability). In contrast, consistency—how similarly (in terms of search speed) an individual spent searching from trial to trial—was the primary predictor for the most experienced professional visual searchers (39% of variability). These results inform cognitive theory by illuminating factors that differentially affect search performance between participants, and real-world issues by identifying search behaviours (consistency in particular) important to experienced professional searchers.     

The composite face illusion: A whole window into our understanding of holistic face perception

Two identical top halves of a face are perceived as being different when their bottom halves belong to different faces, showing that the parts of a face cannot be perceived independently from the whole face. When this visual illusion is inserted in a matching task, observers make more mistakes and/or are slower at matching identical top face halves aligned with different bottom halves than when the bottom halves are spatially offset: The composite face effect. This composite face paradigm has been used in more than 60 studies that have provided information about the specificity and nature of perceptual integration between facial parts (“holistic face perception”), the impairment of this process in acquired prosopagnosia, its developmental course, temporal dynamics, and neural basis. Following a review of the main contributions made with the paradigm, I explain its rationale and strengths, and discuss its methodological parameters, making a number of proposals for its optimal use and refinement in order to improve our understanding of holistic face perception. Finally, I explain how this standard composite face paradigm is fundamentally different than the application to facial parts of a congruency/interference paradigm that has a long tradition in experimental psychology since Stroop (1935), and which was originally developed to measure attentional and response interference between different representations rather than perceptual integration. Moreover, a version of this congruency/interference paradigm used extensively over the past years with composite faces lacks a baseline measure and has decisional, attentional, and stimulus confounds, making the findings of these studies impossible to interpret in terms of holistic perception. I conclude by encouraging researchers in this field to concentrate fully on the standard composite face paradigm, gaze contingency, and other behavioural measures that can help us take one of the most important challenges of visual perception research: Understanding the neural mechanisms of holistic face perception.     

Effects of peripheral eccentricity and head orientation on gaze discrimination

Visual search tasks support a special role for direct gaze in human cognition, while classic gaze judgement tasks suggest the congruency between head orientation and gaze direction plays a central role in gaze perception. Moreover, whether gaze direction can be accurately discriminated in the periphery using covert attention is unknown. In the present study, individual faces in frontal and in deviated head orientations with a direct or an averted gaze were flashed for 150 ms across the visual field; participants focused on a centred fixation while judging the gaze direction. Gaze discrimination speed and accuracy varied with head orientation and eccentricity. The limit of accurate gaze discrimination was less than ±6° eccentricity. Response times suggested a processing facilitation for direct gaze in fovea, irrespective of head orientation, however, by ±3° eccentricity, head orientation started biasing gaze judgements, and this bias increased with eccentricity. Results also suggested a special processing of frontal heads with direct gaze in central vision, rather than a general congruency effect between eye and head cues. Thus, while both head and eye cues contribute to gaze discrimination, their role differs with eccentricity.     

Lecturers' faces fatigue their students: Face identity aftereffects for dynamic and static faces

Face adaptation has been used as a tool to probe our representations for facial identity. It has also been claimed to play a functional role in face processing, perhaps calibrating the visual system towards encountered faces. However, for this to be so, face aftereffects must be observable following adaptation to ecologically valid moving stimuli, not just after prolonged viewing of static images. We adapted our participants to videos, static image sequences or single images of the faces of lecturers who were personally familiar to them. All three stimulus types produced significant, and equivalent, face identity aftereffects, demonstrating that aftereffects are not confined to static images but can occur after exposure to more naturalistic stimuli. It is also further evidence against explanations of face adaptation effects solely in terms of low-level visual processing.     

The role of eye fixations in concentration and amplification effects during multiple object tracking

When tracking spatially extended objects in a multiple object tracking task, attention is preferentially directed to the centres of those objects (attentional concentration), and this effect becomes more pronounced as object length increases (attentional amplification). However, it is unclear whether these effects depend on differences in attentional allocation or differences in eye fixations. We addressed this question by measuring eye fixations in a dual-task paradigm that required participants to track spatially extended objects, while simultaneously detecting probes that appeared at the centres or near the endpoints of objects. Consistent with previous research, we observed concentration and amplification effects: Probes at the centres of objects were detected more readily than those near their endpoints, and this difference increased with object length. Critically, attentional concentration was observed when probes were equated for distance from fixation during free viewing, and concentration and amplification were observed without eye movements during strict fixation. We conclude that these effects reflect the prioritization of covert attention to particular spatial regions within extended objects, and we discuss the role of eye fixations during multiple object tracking.     

Flexible target representations underlie repetition priming in visual search

Repeating target features across consecutive visual search trials can influence response time. Three experiments are reported that show that this repetition priming is dependent on the exact stimulus configuration and feature type. In Experiment 1 the target was defined relative to distractors by its orientation and target colour was task irrelevant. The roles played by these features were reversed in Experiment 2. Repeating target colour across trials speeded responses in both Experiments 1 and 2. Repeating orientation significantly slowed responses in Experiment 1 but had no significant effect in Experiment 2. Existing feature-based and episodic memory-based explanations of priming cannot account for these data, but instead more flexible explanations are required. Experiment 3 showed that significant positive priming results from repeating distractor-defining orientation, indicating that priming of pop-out effects previously reported in the literature may result from combined target and distractor effects.