Super-recognisers: Face recognition performance after variable delay intervals

Outstanding long-term face recognition of suspects is a hallmark of the exceptionally skilled police ‘super-recognisers’ (SRs). Yet, research investigating SR's memory for faces mainly employed brief retention intervals. Therefore, in Experiment 1, 597 participants (121 SRs) viewed 10 target videos and attempted identification of targets from 10 target-present line-ups after 1–56 days. In Experiment 2, 1,421 participants (301 SRs) viewed 20 target videos, and after a baseline of no delay to 28 days,—10 target-present and 10 target-absent line-ups, to assess correct line-up rejections. Overall, delay positively correlated with hits but not with correct rejections. Most, but not all SRs, made more correct identifications and correct rejections than controls at all retention intervals, demonstrating that many SRs possess enhanced long-term face memory. This research adds to the knowledge of SR's skillsets, and enhances the case for the selection of SRs to identity critical roles—particularly policing.     

Face detection dissociates from face identification

We describe three experiments in which viewers complete face detection tasks as well as standard measures of unfamiliar face identification. In the first two studies, participants viewed pareidolic images of objects (Experiment 1) or cloud scenes (Experiment 2), and their propensity to see faces in these scenes was measured. In neither case is performance significantly associated with identification, as measured by the Cambridge Face Memory or Glasgow Face Matching Tests. In Experiment 3 we showed participants real faces in cluttered scenes. Viewers’ ability to detect these faces is unrelated to their identification performance. We conclude that face detection dissociates from face identification.     

Face detection in normal and prosopagnosic individuals

Face detection, the process of finding a face in a visual scene, is a critical step in face processing, yet it has received relatively little attention compared with other face processes. The present study addresses this crucial first stage by investigating the effect of inversion on face detection and by examining how individuals with developmental prosopagnosia perform on face detection tasks. Fourteen control participants and fourteen individuals with developmental prosopagnosia (DPs) were tested with two face detection tasks: (1) Face versus Non‐Face, where arrays of small images were presented, one of which could contain a face and (2) Face versus Face Parts, where a two‐tone face could be embedded in a larger array of similar two‐tone face parts. On each trial, participants made a speeded response if a face was present in the visual display. On almost all measures both normal and prosopagnosic individuals showed strong inversion effects with significantly worse performance with inverted faces. This shows that the simple task of detection can show inversion effects comparable to those seen for other face tasks, including recognition. Finally, while there were prosopagnosics who were well within the normal range for detection, there were significant group differences, particularly for the case of the Face versus Face Parts, where prosopagnosics were worse than controls on upright but not on inverted face detection.     

Face distinctiveness and delayed testing: differential effects on performance and confidence

The author investigated the effect of delayed testing on participants' memory for distinctive and typical faces. Participants viewed distinctive and typical faces and were then tested for recognition immediately or after a delay of 3, 6, or 12 weeks. Consistent with prior research, analysis of measure of sensitivity (d') showed that participants performed better on distinctive rather than typical faces, and memory performance declined with longer retention intervals between study and testing. Furthermore, the superior performance on distinctive faces had vanished by the 12-week test. Contrary to d' data, however, an analysis of confidence scores indicated that participants were still significantly more confident on trials depicting distinctive faces, even with a 12-week delay between study and recognition testing.     

Face detection differs from categorization: Evidence from visual search in natural scenes

In this study, we examined whether the detection of frontal, ¾, and profile face views differs from their categorization as faces. In Experiment 1, we compared three tasks that required observers to determine the presence or absence of a face, but varied in the extents to which participants had to search for the faces in simple displays and in small or large scenes to make this decision. Performance was equivalent for all of the face views in simple displays and small scenes, but it was notably slower for profile views when this required the search for faces in extended scene displays. This search effect was confirmed in Experiment 2, in which we compared observers’ eye movements with their response times to faces in visual scenes. These results demonstrate that the categorization of faces at fixation is dissociable from the detection of faces in space. Consequently, we suggest that face detection should be studied with extended visual displays, such as natural scenes.     

Language representation in the human brain: evidence from cortical mapping

The manner in which the human brain processes grammatical-syntactic and lexical-semantic functions has been extensively debated in neurolinguistics. The discreteness and selectivity of the representation of syntactic-morphological properties in the dominant frontal cortex and the representation of the lexical-semantics in the temporo-parietal cortex have been questioned. Three right-handed adult male neurosurgical patients undergoing left craniotomy for intractable seizures were evaluated using various grammatical and semantic tasks during cortical mapping. The sampling of language tasks consisted of trials with stimulation (experimental) and without stimulation (control) from sites in the dominant fronto-temporo-parietal cortex The sampling of language implicated a larger cortical area devoted to language (syntactic-morphological and lexical-semantic) tasks. Further, a large part of the fronto-parieto-temporal cortex was involved with syntactic-morphological functions. However, only the parieto-temporal sites were implicated with the ordering of lexicon in sentence construction. These observations suggest that the representation of language in the human brain may be columnar or multilayered.     

行为遗传学：解决面孔特异性问题争论的新思

面孔刺激的加工存在特异性,但“特异性”的具体内涵仍存在争议。面孔特异性假说认为面孔刺激具有特异性;而专家假说则认为存在特异性的是整体加工的模式。通过对相关领域近年来主要的研究结果的总结,发现争论中混淆了两个概念——加工类型和刺激类型,二者正交分解可将争论归纳为三个假设：1）面孔整体加工特异性的假设;2）面孔刺激特异性的假设;3）专家加工特异性的假设。在未来的研究中,行为遗传学可为解决该争论提供合适的方法     

Face to face with an enactive approach: A sensorimotor account of face detection and recognition

The enactive approach to perception describes experience as a temporally extended activity of skillful engagement with the environment. This paper pursues this view and focuses on prosopagnosia both for the light that the theory can throw on the phenomenon, and for the critical light the phenomenon can throw on the theory. I argue that the enactive theory is insufficient to characterize the unique nature of experience specific to prosopagnosic subjects. There is a distinct difference in the overall process of detection (with respect to eye movement sequence) of familiar and unfamiliar faces in prosopagnosia; in contrast, normal subjects use the same scanning strategy when exploring both kinds of faces despite an obvious difference in qualitative character. In light of this limitation I outline a supplemental view basing sensorimotor contingencies upon the establishment and reaffirmation of regularities within the organism as it engages with the environment.     

Controlling human fixed-interval performance

Both high and relatively constant rates of responding without post-reinforcement pauses and lower rates with pauses after reinforcement are produced by human subjects under fixed-interval (FI) schedules. Such FI rates and patterns may be controlled when subjects are provided with different histories of conditioning and different conditions of response cost (reinforcement penalties per response). Subjects with a conditioning history under ratio schedules typically produce high and relatively constant rates of responding under FI schedules; this responding does not change systematically with changes in FI value. In contrast, subjects with a history under schedules which produce little or no responding between reforcements [such as differential-reinforcement-of-low-rate (DRL) schedules] tend to pause after reinforcement and respond at low rates under FI schedules, whether or not they also have ratio conditioning histories; cost increases the likelihood of this type of performance. For DRL-history subjects, post-reinforcement pauses increase and response rates decrease as FI values increase.     

行为遗传学:解决面孔特异性问题争论的新思路

面孔刺激的加工存在特异性,但"特异性"的具体内涵仍存在争议.面孔特异性假说认为面孔刺激具有特异性;而专家假说则认为存在特异性的是整体加工的模式.通过对相关领域近年来主要的研究结果的总结,发现争论中混淆了两个概念--加工类型和刺激类型,二者正交分解可将争论归纳为三个假设:1)面孔整体加工特异性的假设;2)面孔刺激特异性的假设;3)专家加工特异性的假设.在未来的研究中,行为遗传学可为解决该争论提供合适的方法.     

Noise effects on human performance: a meta-analytic synthesis

Noise is a pervasive and influential source of stress. Whether through the acute effects of impulse noise or the chronic influence of prolonged exposure, the challenge of noise confronts many who must accomplish vital performance duties in its presence. Although noise has diffuse effects, which are shared in common with many other chronic forms of stress, it also exerts its own specific influences on various forms of cognitive and motor response. We present a quantitative evaluation of these influences so that their harmful effects can be mitigated, their beneficial effects exploited, and any residual effects incorporated and synthesized into selection, training, and design strategies to facilitate human performance capacities. Predictions of single and joint moderator effects were made on the basis of major theories of noise and performance, specifically those explanations based on arousal, masking, or cognitive-resource mechanisms. These predictions were tested through moderator analyses of effects as a function of task type, performance measure, noise type and schedule, and the intensity and duration of exposure. Observed outcome effects (797 effect sizes derived from 242 studies) varied as a function of each of these moderators. Collective findings identified continuous versus intermittent noise, noise type, and type of task as the major distinguishing characteristics that moderated response. Mixed evidence was obtained for the traditional arousal and masking explanations for noise effects. The overall pattern of findings was most consistent with the maximal adaptability theory, a mental-resource-based explanation of stress and performance variation.     

Journal of experimental psychology: human perception and performance

We examined the nonveridicality of visual direction produced by monocular viewing. In Experiment 1, 19 subjects pointed to a small light and moved a small light to their subjective median plane. The extent of constant error under monocular and binocular viewing conditions differed in both tasks (p less than .001). The monocular-binocular difference was larger when the viewing distance was 25 cm than when it was 50 cm (p less than .01). Also, correlations between phoria and monocular-binocular differences ranged from .58 to .77, depending on viewing distances and tasks. The effects of phoria within the context of Hering's .001). The monocular-binocular difference was larger when the viewing distance was 25 cm than when it was 50 cm (p less than .01). Also, correlations between phoria and monocular-binocular differences ranged from .58 to .77, depending on viewing distances and tasks. The effects of phoria within the context of Hering's .001). The monocular-binocular difference was larger when the viewing distance was 25 cm than when it was 50 cm (p less than .01). Also, correlations between phoria and monocular-binocular differences ranged from .58 to .77, depending on viewing distances and tasks. The effects of phoria within the context of Hering's principle of visual direction can account for these results. In Experiment 2, the same subjects adapted to phoria-induced error by placing a finger over a monocularly viewed target. The difference in their pointing responses before and after the task were reliable (p less than .005), and the correlations between phoria and the pre- to posttest differences were .45 and .77, depending on the number of adaptation trials. We argue that all monocular experiments dealing with visual direction should control for these effects.     

Face to Face

In “Face to Face,” I explore my work as a Jewish analyst with a Lebanese woman, Ara, who is strongly identified with the Palestinian cause. As the work unfolded I find myself thrust into a psychic and social space I had not wanted to inhabit, into the Israeli–Palestinian conflict and the turmoil of Jewish identity. Ara and I were in the midst of ghosts of historical traumas, intersecting and interweaving history and identity between us. It was her history and my history and the history of nations, of broken bonds and damaged victims suddenly all present in the room. I will hold together, in tension, the micro and the macro, the intrapsychic and social, the drama of the encounter between Ara and me and between Palestinians and Jews. I ask what it takes to find one's way into an understanding of the other, a recognition of the other and the legitimacy of their suffering when one's own history is suffused with the trauma of centuries of victimhood. “Face to Face” is an exploration of how to inhabit the Other, how to negotiate difference, moving beyond the dynamics of victim and victimizer, beyond that of oppressor and oppressed to what Emmanuel Levinas refers to as a welcoming of the stranger, a transcendent experience.     

Deferred decision in human signal detection: A preliminary experiment

In the detection task characterized by deferred decision, the observer is allowed to determine how many observations he will make before deciding whether or not a signal is present, and he is called upon to balance the goals of maximizing accuracy and conserving time. The human observer appears capable of using the optimal process of cumulating sensory information over successive observations, but certain common training procedures lead him to use a less efficient process. Though he displays a consistent decision bias, his performance is also in good agreement with the optimal model of the process of terminating a sequence of observations.     

Uncertainty impairs grating detection performance in the cat

Using behavioral techniques, contrast thresholds for detection of grating patterns by the cat were measured under conditions of certainty and uncertainty. For certainty trials, the same combination of spatial and temporal frequencies was presented throughout a test session, whereas with uncertainty, the cat was unable to anticipate which of two spatial (or temporal) frequencies would be presented on a given trial. For most spatiotemporal combinations, uncertainty served to elevate contrast thresholds by almost .3 log units, a finding that parallels the outcome found in human vision. The uncertainty paradigm may provide a useful inferential tool for determining channel bandwidth in cat vision.     

Species differences in temporal control of behavior II: human performance

Human subjects responded on two panels. A differential-reinforcement-of-low-rate schedule with a limited-hold contingency operated on Panel A. In Condition 1, responses on Panel B produced a stimulus on the panel that signalled whether reinforcement was available on Panel A. In Condition 2, responses on Panel B briefly illuminated a digital clock. In both conditions, performance on Panel A was very efficient; with few exceptions, Panel A was pressed only when reinforcement was available. Thus, in effect, a fixed-interval schedule operated on Panel B. In Condition 1, a “break-and-run” response pattern occurred on Panel B; with increasing temporal parameters, the duration of the postreinforcement pause on Panel B increased linearly while overall response rate and running rate (calculated by excluding the postreinforcement pauses) remained approximately constant. In Condition 2, the response pattern on Panel B was scalloped; the postreinforcement pause was a negatively accelerated increasing function of schedule value, while overall response rate and running rate were negatively accelerated decreasing functions of schedule value. The performance of subjects in Condition 2, but not in Condition 1, was highly sensitive to the contingencies in operation, and resembled that of other species on the fixed-interval schedule.