Árni Gunnar Ásgeirsson

Episodic retrieval and feature facilitation in intertrial priming of visual search

Huang, Holcombe, and Pashler (Memory & Cognition, 32, 12–20, 2004) found that priming from repetition of different features of a target in a visual search task resulted in significant response time (RT) reductions when both target brightness and size were repeated. But when only one feature was repeated and the other changed, RTs were longer than when neither feature was repeated. From this, they argued that priming in visual search reflected episodic retrieval of memory traces, rather than facilitation of repeated features. We tested different variations of the search task introduced by Huang et al., with the aim of uncovering when priming is episodic and when feature based. We found that varying the signal strength of target against distractors had a strong effect on the priming pattern. In difficult search with low signal-to-noise ratios of target against distractors, the priming patterns were episodic. When feature contrasts between target and distractors were increased, priming of different features was independent and additive. Our results suggest that, during inefficient search,priming can be episodic but that, for more efficient search, priming from different features occurs independently. The results support two-stage (or multistage) accounts of priming in visual search.

Saccade performance in the nasal and temporal hemifields

There are numerous asymmetries in anatomy between the nasal and temporal hemiretinae, which have been connected to various asymmetries in behavioral performance. These include asymmetries in Vernier acuity, saccade selection, and attentional function, in addition to some evidence for latency differences for saccadic eye movements. There is also evidence for stronger retinotectal neural projection from the nasal than the temporal hemiretina. There is, accordingly, good reason to predict asymmetries in saccadic performance depending on which hemifield the saccade trigger stimuli are presented in, but the evidence on this is mixed. We tested for asymmetries in both saccade latency and landing point accuracy in a variety of different saccade tasks. We found no evidence for any asymmetries in saccade latency and only modest evidence for asymmetries in landing point accuracy. While this lack of asymmetry is surprising in light of previous findings of attentional asymmetries, it may reflect that cortical input to midbrain eye control centers mitigates any retinal and retinotectal asymmetry.

Repetition priming in selective attention: A TVA analysis

Current behavior is influenced by events in the recent past. In visual attention, this is expressed in many variations of priming effects. Here, we investigate color priming in a brief exposure digit-recognition task. Observers performed a masked odd-one-out singleton recognition task where the target-color either repeated or changed between subsequent trials. Performance was measured by recognition accuracy over exposure durations. The purpose of the study was to replicate earlier findings of perceptual priming in brief displays and to model those results based on a Theory of Visual Attention (TVA; Bundesen, 1990). We tested 4 different definitions of a generic TVA-model and assessed their explanatory power. Our hypothesis was that priming effects could be explained by selective mechanisms, and that target-color repetitions would only affect the selectivity parameter (α) of our models. Repeating target colors enhanced performance for all 12 observers. As predicted, this was only true under conditions that required selection of a target among distractors, but not when a target was presented alone. Model fits by TVA were obtained with a trial-by-trial maximum likelihood estimation procedure that estimated 4-15 free parameters, depending on the particular model. We draw two main conclusions. Color priming can be modeled simply as a change in selectivity between conditions of repetition or swap of target color. Depending on the desired resolution of analysis; priming can accurately be modeled by a simple four parameter model, where VSTM capacity and spatial biases of attention are ignored, or more fine-grained by a 10 parameter model that takes these aspects into account.

Random reward priming is task-contingent: the robustness of the 1-trial reward priming effect

Consistent financial reward of particular features influences the allocation of visual attention in many ways. More surprising are 1-trial reward priming effects on attention where reward schedules are random and reward on one trial influences attentional allocation on the next. Those findings are thought to reflect that rewarded features become more salient than unrewarded ones on the subsequent trial. Here we attempt to conceptually replicate this effect, testing its generalizability. In three versions of an analogous paradigm to the additional singleton paradigm involving singleton search for a Gabor patch of odd spatial frequency we found no evidence of reward priming, while we only partially replicate the reward priming in the exact original paradigm tested by Hickey and colleagues. The results cast doubt on the proposal that random reward enhances salience, suggested in the original papers, and highlight the need for a more nuanced account. In many other paradigms reward effects have been found to progress gradually, becoming stronger as they build up, and we argue that for robust reward priming, reward schedules need to be more consistent than in the original 1-trial reward priming paradigm.

Components of Attention in Grapheme-Color Synesthesia: A Modeling Approach

Grapheme-color synesthesia is a condition where the perception of graphemes consistently and automatically evokes an experience of non-physical color. Many have studied how synesthesia affects the processing of achromatic graphemes, but less is known about the synesthetic processing of physically colored graphemes. Here, we investigated how the visual processing of colored letters is affected by the congruence or incongruence of synesthetic grapheme-color associations. We briefly presented graphemes (10–150 ms) to 9 grapheme-color synesthetes and to 9 control observers. Their task was to report as many letters (targets) as possible, while ignoring digit (distractors). Graphemes were either congruently or incongruently colored with the synesthetes’ reported grapheme-color association. A mathematical model, based on Bundesen’s (1990) Theory of Visual Attention (TVA), was fitted to each observer’s data, allowing us to estimate discrete components of visual attention. The models suggested that the synesthetes processed congruent letters faster than incongruent ones, and that they were able to retain more congruent letters in visual short-term memory, while the control group’s model parameters were not significantly affected by congruence. The increase in processing speed, when synesthetes process congruent letters, suggests that synesthesia affects the processing of letters at a perceptual level. To account for the benefit in processing speed, we propose that synesthetic associations become integrated into the categories of graphemes, and that letter colors are considered as evidence for making certain perceptual categorizations in the visual system. We also propose that enhanced visual short-term memory capacity for congruently colored graphemes can be explained by the synesthetes’ expertise regarding their specific grapheme-color associations.

No arousal-biased competition in focused visuospatial attention

Arousal sometimes enhances and sometimes impairs perception and memory. A recent theory attempts to reconcile these findings by proposing that arousal amplifies the competition between stimulus representations, strengthening already strong representations and weakening already weak representations. Here, we report a stringent test of this arousal-biased competition theory in the context of focused visuospatial attention. Participants were required to identify a briefly presented target in the context of multiple distractors, which varied in the degree to which they competed for representation with the target, as revealed by psychophysics. We manipulated arousal using emotionally arousing pictures (Experiment 1), alerting tones (Experiment 2) and white-noise stimulation (Experiment 3), and validated these manipulations with electroencephalography and pupillometry. In none of the experiments did we find evidence that arousal modulated the effect of distractor competition on the accuracy of target identification. Bayesian statistics revealed moderate to strong evidence against arousal-biased competition. Modeling of the psychophysical data based on Bundesens (1990) theory of visual attention corroborated the conclusion that arousal does not bias competition in focused visuospatial attention.

Synesthesia induced colors do not bias attention in the same manner as physical colors do

Grapheme-color synesthesia affects visual cognition in significant ways. The congruence or incongruence of physical stimuli with synesthetic color affects how quickly and accurately synesthetes respond to stimuli, and the induced color experience may help them memorize achromatic material and performance in visual search, much like physical stimulus features. It has been demonstrated that the content of visual memory can guide attention (e.g. Carlisle & Woodman, 2011). This effect can be measured in the response time costs or benefits related to the presence of memorized color in a visual search display. Retaining color information in memory biases attention towards that specific color in visual search, apparent by response time costs when a matching distractor is present, but a benefit when the target matches the retained color. We investigated whether a synesthetic color is automatically represented in visual memory of observers with color-grapheme synesthesia, and consequently biases attention towards the synesthesia congruent stimuli. A group of synesthetes performed a memory task combined with a visual search for colored Landolt squares to explore this question. Each trial started with the presentation of an achromatic letter, followed by a visual search display. There were three types of search trials; 1) where the target color matched the color associated with the memorized letter, 2) where a distractor color matched the letter, and 3) where the associated color was absent from display. Finally, participants responded to memory probe to ensure that the letter was memorized. We found no significant differences in response times dependent on synesthetically induced colors. However, there were clear costs and benefits of having physical colors in visual memory. This suggests that - unlike physical color - synesthetic colors are not automatically represented in visual memory. Meeting abstract presented at VSS 2015.

Dissociating Contents of Consciousness from Contents of Short-Term Memory

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