Inhibition of return (IOR) is an inhibitory aftereffect of visuospatial orienting, typically resulting in slower responses to targets presented in an area that has been recently attended. Since its discovery, myriad research has sought to explain the causes and effects underlying this phenomenon. Here, we briefly summarize the history of the phenomenon, and describe the early work supporting the functional significance of IOR as a foraging facilitator. We then shine a light on the discordance in the literature with respect to mechanism — in particular the lack of theoretical constructs that can consistently explain innumerable dissociations. We then describe three diagnostics (central arrow targets, locus of slack logic and the psychological refractory period, and performance in speed-accuracy space) used to support our theory that there are two forms of inhibition of return — the form which is manifest being contingent upon the activation state of the reflexive oculomotor system. The input form, which operates to decrease the salience of inputs, is generated when the reflexive oculomotor system is suppressed; the output form, which operates to bias responding, is generated when the reflexive oculomotor system is not suppressed. Then, we subject a published data set, where inhibitory effects had been generated while the reflexive oculomotor system was either active or suppressed, to diffusion modeling. As we hypothesized, based on the aforementioned theory, the effects of the two forms of IOR were best accounted for by different drift diffusion parameters.
Inhibition of return (IOR) represents a delay in responding to a previously inspected location and is viewed as a crucial mechanism that sways attention toward novelty in visual search. Although most visual processing occurs in retinotopic, eye-centered, coordinates, IOR must be coded in spatiotopic, environmental, coordinates to successfully serve its role as a foraging facilitator. Early studies supported this suggestion but recent results have shown that both spatiotopic and retinotopic reference frames of IOR may co-exist. The present study tested possible sources for IOR at the retinotopic location including being part of the spatiotopic IOR gradient, part of hemifield inhibition and being an independent source of IOR. We conducted four experiments that alternated the cue-target spatial distance (discrete and contiguous) and the response modality (manual and saccadic). In all experiments, we tested spatiotopic, retinotopic and neutral (neither spatiotopic nor retinotopic) locations. We did find IOR at both the retinotopic and spatiotopic locations but no evidence for an independent source of retinotopic IOR for either of the response modalities. In fact, we observed the spread of IOR across entire validly cued hemifield including at neutral locations. We conclude that these results indicate a strategy to inhibit the whole cued hemifield or suggest a large horizontal gradient around the spatiotopically cued location.
Chromatic stimuli across a boundary of basic color categories (BCCs; eg blue and green) are discriminated faster than colorimetrically equidistant colors within a given category. Russian has two BCCs for blue, sinij 'dark blue' and goluboj 'light blue'. These language-specific BCCs were reported to enable native Russian speakers to discriminate cross-boundary dark and light blues faster than English speakers (Winawer et al., 2007, PNAS, 4, 7780-7785). We re-evaluated this finding in two experiments that employed identical tasks as in the cited study. In Experiment 1, Russian and English speakers categorized colors as sinij / goluboj or dark blue / light blue respectively; this was followed by a color discrimination task. In experiment 2 Russian speakers initially performed the discrimination task on sinij / goluboj and goluboj / zelënyj 'green' sets. They then categorized these colors in three frequency contexts with each stimulus presented: (i) an equal number of times (unbiased); more frequent (ii) either sinij or goluboj; (iii) either goluboj or zelënyj. We observed a boundary response speed advantage for goluboj / zelënyj but not for sinij / goluboj. The frequency bias affected only the sinij / goluboj boundary such that in a lighter context, the boundary shifted towards lighter shades, and vice versa. Contrary to previous research, our results show that in Russian, stimulus discrimination at the lightnessdefined blue BCC boundary is not reflected in processing speed. The sinij / goluboj boundary did have a sharper categorical transition than the dark blue / light blue boundary,
Since the 1990s, there has been an ongoing discussion in religious studies about the uses of the terms “secular” and “religious.” This article applies the methodology of the critical study of religion within the psychology of religion. There are two main strategies to construct a research program in this field: (1) studying how religious senses occur (neurotheology, transpersonal psychology) and (2) studying how religious representations emerge (cognitive religious studies). This paper provides an overview of these two paradigms through the lens of the religious/secular dichotomy. Scholars who are trying to understand the nature of religious phenomena ignore a significant amount of data labeled as “secular.” The author then suggests studying such representations or senses beyond the religious/secular dichotomy.
Medial frontal cortex is currently viewed as the main hub of the performance monitoring system; upon detection of an error committed, it establishes functional connections with brain regions involved in task performance, thus leading to neural adjustments in them. Previous research has identified targets of such adjustments in the dorsolateral prefrontal cortex, posterior cortical regions, motor cortical areas, and subthalamic nucleus. Yet most of such studies involved visual tasks with relatively moderate cognitive load and strong dependence on motor inhibition – thus highlighting sensory, executive and motor effects while underestimating sensorimotor transformation and related aspects of decision making. Currently there is ample evidence that posterior parietal cortical areas are involved in task-specific neural processes of decision making (including evidence accumulation, sensorimotor transformation, attention, etc.) – yet, to our knowledge, no EEG studies have demonstrated post-error increase in functional connectivity in the theta-band between midfrontal and posterior parietal areas during performance on non-visual tasks. In the present study, we recorded EEG while subjects were performing an auditory version of the cognitively demanding attentional condensation task; this task involves rather non-straightforward stimulus-to-response mapping rules, thus, creating increased load on sensorimotor transformation. We observed strong pre-response alpha-band suppression in the left parietal area, which presumably reflected involvement of the posterior parietal cortex in task-specific decision-making processes. Negative feedback was followed by increased midfrontal theta-band power and increased functional coupling in the theta band between midfrontal and left parietal regions. This could be interpreted as activation of the performance monitoring system and top–down influence of this system on the posterior parietal regions involved in decision making, respectively. This inter-site coupling related to negative feedback was stronger for subjects who tended to commit errors with slower response times. Generally, current findings support the idea that slower errors are related to the state of outcome uncertainty caused by failures of task-specific processes, associated with posterior parietal regions.
Microsaccadic eye movements belong to the category of micromovements, such as tremor and drift, though their functional purpose is still debated. Spatial cueing paradigms typically require fixational control, but this does not eliminate all oculomotor activity associated with the preparation of saccades in the cued direction. During the antisaccade task, planning and execution are separate processes and we therefore hypothesise that we may notice reduced microsaccade behaviour during the execution of antisaccade tasks as compared to saccade trials. The study is based on an eyetracking experiment involving 22 participants asked to perform saccades and antisaccades in blocked or mixed sets of trials. Each participant contributed to three main blocks: 50 trials in the fixed saccade block, 50 trials in the fixed antisaccade block, and 200 trials in the mixed saccade — antisaccade condition. In the saccade trials, a green fixation cross is displayed at the centre of the screen, whereas during the antisaccade trials the fixation cross is red, allowing participants to prepare the appropriate response (but not direction) prior to the target. The results of the study imply a strong latency cost of antisaccades as compared to prosaccades and an additional cost of mixed blocks, though these two effects did not interact. Crucially, in the blocked antisaccade trials, we predict that a supressed oculomotor system would lead to a lower occurrence of microsaccades initiated by the participants, in particular the trials where observers did not make erroneous prosaccades. We believe this may be due to participants having enough time to prepare the top-down control of the oculomotor system, which leads to a predictable pattern for each participant, where they either suppress microsaccadic movements completely or do not throughout the entire block. We also predict that in the mixed block participants have less time to prepare the top-down microsaccade suppression and we will test this by comparing data between the saccade, the antisaccade and mixed blocks
The allocation of attention can occur not only in space, but also in time. Application of Rescorla's "truly random control" procedure about independency of cues and targets allowed us to differentiate the impact of endogenous (voluntary) and exogenous (automatic) components of temporal attention on the performance separately and within their interaction. In a random dot motion task, variation of luminance and motion of dots, that represent the cue, affects the engagement of exogenous mode. Temporal contingency between cues and targets or its absence affects the impact of endogenous mode. Combining these conditions, the results are as follows. For endogenous cues, we see improvement of both speed and accuracy at early cue target onset asynchrony. For exogenous cues, we see improvement of response times, but not accuracy. When both are involved, we observe a trade-off of speed and accuracy. This parallels from the auditory modalities of alertness cueing but with purely visual stimuli.
The classic Saliency Model by Itti and Koch launched many studies that contributed to the modelling of layers for vision and visual attention. The aim of this study is to improve the existing saliency model by using a neural network to generate salience maps to model human saccade generation. The proposed model uses a Leaky Integrate-and-Fire layer for temporal predictions, and replaces spatial salience with a deep learning neural network in order to create a generative model that combines spatial and temporal predictions. The results involve a deep neural network which is able to predict eye movements based on unsupervised learning from raw image input, as well as supervised learning from fixation maps retrieved during an eye-tracking experiment with 35 participants at later stages in order to train a 2D softmax layer. The results imply that it is possible to match model human fixation locations but temporal distributions are still limited by the accuracy of the leaky algorithm.
As a foraging facilitator, Inhibition of return (IOR) must be coded in spatiotopic coordinates. Early reports confirmed this suggestion but these results have been recently challenged. The present study was designed to examine the reference frame of IOR and to test whether retinotopic IOR might be a part of the spatiotopic IOR gradient. We conducted four experiments with spatiotopically and retinotopically cued coordinates and an intervening saccade between the cue and target presentations. We alternated the response modality (manual and saccadic) and the cue-target spatial distance (fixed and contiguous). Our data showed evidence for an independent source of retinotopic IOR neither at discrete locations nor as a gradient; moreover, we observed the spread of IOR across the whole validly cued hemifield. We propose that these results indicate a strategy to attend and then inhibit the entire cued hemifield.
Transcranial alternating current stimulation (tACS) can be used to modulate brain activity. tACS was shown to induce frequency-, state-, and phase- dependent effects which makes tACS a neurostimulation technique that provides a more valuable predictable outcome. However, the impact of different tACS intensities has not been systematically investigated yet. Here, we proposed to investigate the effects of tACS of the primary motor cortex (M1) delivered at different intensities.
There is a common assumption that application of stimulation for longer duration or for higher intensity leads to more reliable physiological and behavioral effects. However, previous studies performed using different transcranial electrical stimulation methods such as transcranial direct current stimulation (tDCS) and/or at high-frequency such as tACS at ripple range, showed non-monotonic effect of stimulation intensity. Nevertheless, tDCS and high-frequency tACS potentially rely on different mechanisms of neuromodulation with respect to conventional tACS delivered at EEG range (1 – 70 Hz).
In this study we applied 20 Hz tACS to the primary motor cortex (M1) to investigate potential non-monotonic effect of tACS intensities (ranging from 0.25 mA to 2 mA with 0.25 mA interval between conditions) on the M1 excitability measured as the peak-to-peak amplitude of TMS-induced motor evoked potentials (MEPs). As for control, we used 1 mA 10 Hz (alpha) tACS and a no stimulation condition.
Preliminary results (N = 9) showed increase of MEPs for higher intensities (1.5 mA, 2 mA) of stimulation. In addition, an interesting effect emerged for those subjects with a lower motor threshold which showed a higher MEPs modulation effect of beta-tACS
Transcranial direct current stimulation (tDCS) is a promising tool for modulation of learning and memory, allowing to transiently change cortical excitability of specific brain regions with physiological and behavioral outcomes. A detailed exploration of factors that can moderate tDCS effects on episodic long-term memory (LTM) is of high interest due to the clinical potential for patients with traumatic or pathological memory deficits and with cognitive impairments. This commentary discusses findings by Marián et al. (2018) recently published in Cortex within a broad context of brain stimulation in memory research.
Background Used / introduction of The early eye tracking studies of descriptive Yarbus Provided Evidence That an observer's task Influences patterns of eye Movements, a leading to the a tantalizing prospect That an observer's Intentions Could the BE inferred from Their saccade behavior. This is a dynamic and dynamic cognitive companion using a Dynamic Bayesian Network (DBN). Understanding how it comes to human cognitive goals. This model provides a Bayesian, cognitive approach to pre-frontal areas with the colliculus. This method has been previously shown. This is an analysis of the observer’s task. Secondly, it is a state cognitive state . Finally, we ’ve been able to make a difference . Results This is the only factor that influences observers' saccadic behavior. It has been shown that it has been shown that it has been selected for the paradigms. Conclusions Given the generative nature of this model in real time. We have shown that it has been closely coordinated with those of human observers. Many current models of vision The area of interest is within the visual scene. There are three ways to add top-down knowledge and knowledge . First of all, it is given the information available to the visual system. Matches influential theories This of bias signals by Miller & Cohen (2001), and implements selection of state without simply shifting the decision to an external homunculus. Second, our model is a generative and capable of those found in visual search. Third, our model generates relative saccadic vector information as opposed to absolute spatial coordinates. This match is more closely associated with the colliculus.
People often miss them. This phenomenon, reveals the limits of visual awareness. Here, we will investigate the blindness of the patient. Traditional gazecontingent paradigms adapt the display in real time. We’ll compare you with a mouse-contingent paradigm for your mouse. 2) and untethered overt and covert attention (mousecontingent display; Experiment 1). In the case of a person who has been in a state of discomfort, it can lead to change blindness. The results of the show are processed. In addition, there is a need for further changes to the changing target. Finally, it’s possible to establish a direct connection. The results of the show are processed. In addition, there is a need for further changes to the changing target. Finally, it’s possible to establish a direct connection. The results of the show are processed. In addition, there is a need for further changes to the changing target. Finally, it’s possible to establish a direct connection.
People often miss salient events that occur right in front of them. This phenomenon, known as change blindness, reveals the limits of visual awareness. Here, we investigate the role of implicit processing in change blindness using an approach that allows partial dissociation of covert and overt attention. Traditional gaze-contingent paradigms adapt the display in real time according to current gaze position. We compare such a paradigm with a newly designed mouse-contingent paradigm where the visual display changes according to the real-time location of a user-controlled mouse cursor, effectively allowing comparison of change detection with mainly overt attention (gaze-contingent display; Experiment 2) and untethered overt and covert attention (mouse-contingent display; Experiment 1). We investigate implicit indices of target detection during change blindness in eye movement and behavioral data, and test whether affective devaluation of unnoticed targets may contribute to change blindness. The results show that unnoticed targets are processed implicitly, but that the processing is shallower than if the target is consciously detected. Additionally, the partial untethering of covert attention with the mouse-contingent display changes the pattern of search and leads to faster detection of the changing target. Finally, although it remains possible that the deployment of covert attention is linked to implicit processing, the results fall short of establishing a direct connection.
Attending a location in short space. Certain types of exogenous cues - such as sudden peripheral onsets - have been described as reflexive and automatic. However, it has been shown that it has been shown. However, it doesn’t automatically consider this location. It is a test of exogenous responses. We've seen such as saccadic curvature, microsaccades and pupil size. It can be measured as the result of the reaction time. There is no need for a microsaccade after the cue. It was the effect that the process of recovery was observed. It has been shown to be there in a field. Overall, we'll find it in pupil size. It is indicative of whether we see RT or facilitation or not. Microsaccades were not diagnostic in either experiment. Finally, there is no need for any response measures.
It has been noted that it has been the case that it has been recognized as a paradigm. Krüger, MacInnes, and Hunt (2014) propose that it is possible to re-enterrant processing. In the case of experiments, we’ve been working on the asynchrony (CTOA) ranging from -300 to + 1000ms. An analysis of the reaction time has been shown in the analysis of the reaction time. . In the experiment, we’ve eliminated the need for restriction, and (b) the discrete, and (c) blocked discrete CTOAs. Results obtained in the continuous and binned conditions showed no facilitation but robust IOR. We found both early facilitation and IOR in the blocked condition. Overall, he received a suggestion of different underlying mechanisms. Second,