Increase in speed eliminates duration expansion of a novel motion stimulus.

A novel motion stimulus is perceived to last longer than the subsequent motion stimulus moving in the opposite direction. A previous study suggested that the discrepancy in the processing latency for different onset types, as measured by reaction time, may play a role in this duration expansion. The present study examined whether the speed of motion stimuli influences this duration expansion. Experiment 1 demonstrated that the duration expansion ceased to occur when the stimulus speed increased. Experiment 2 showed that the increase in the speed reduced the reaction time for various onset types. However, the size of the changes in the reaction time did not match the reduction in the magnitude of the duration expansion observed in Experiment 1. These results suggest that the increase in speed eliminates the duration expansion of the novel motion stimulus, but the difference in the processing latency alone may not be the sole mechanism.

Face adaptation induces duration distortion of subsequent face stimuli in a face category-specific manner.

Studies have shown that duration perception depends on several visual processes. However, the stages of visual processes that contribute to duration perception remain unclear. This study examined the effects of categorical differences in face adaptation on perceived duration. In all the experiments, we compared the perceived durations of human, monkey, and cat faces (comparison stimuli) after adapting to a human face. Results revealed that the human comparison stimuli were perceived shorter than the monkey and cat comparison stimuli (categorical face adaptation on duration perception [CFAD]). The difference between the face categories disappeared when the adapting stimulus was rendered unrecognizable by phase scrambling, indicating that adaptation to low-level visual properties cannot fully account for the CFAD effect. Furthermore, CFAD was preserved but attenuated when the adapting stimulus was inverted or a 1,000-ms interval was inserted before the comparison stimuli, which implied that CFAD occurred as long as the adapting stimulus was perceived as a face and not simply based on conceptual category processes. These findings indicate that face adaptation affects perceived duration in a category-specific manner (the CFAD effect) and highlights the involvement of visual categorical processes in duration perception.

Visual images of disgusting creatures facilitated attentional orienting and delayed attentional disengagement.

Numerous studies have suggested that threatening stimuli induce a spatial attention bias; however, only a few studies have investigated spatial attention biases for disgusting stimuli. Moreover, past studies generally reported that the spatial attention bias to disgusting images is not robustly in normal individuals. We hypothesized that this was due to the unfamiliar of the images, so we prepared the creature's images that were clearly categorized as disgusting and examined the effects of disgusting images on spatial attention bias. A disgusting or an emotionally neutral image was paired and presented with an (emotionally neutral) filler image. After a temporal interval, a target appeared at either the position where a disgusting or a neutral image was presented (valid condition) or where a filler image was presented (invalid condition). Participants pressed a key corresponding to the target's position as quickly and accurately as possible. We varied the position-response correspondence among three experiments. The results showed that the RTs in the invalid condition was longer for the disgusting images than for the neutral images when the position of a disgusting image was not naturally associated with the left-right hand position. We interpreted the results in that that disgusting images generally slowed down attentional disengagement process but the manual responses were inhibited for the position where a disgusting image appeared when the locations of keys and targets were congruent. The present results suggest that disgusting images affect not only attentional processes but also manual responses related to the selection and initiation of responses.

Corticospinal excitability and somatosensory information processing of the lower limb muscle during upper limb voluntary or electrically induced muscle contractions.

Neural interactions between upper and lower limbs underlie motor coordination in humans. Specifically, upper limb voluntary muscle contraction can facilitate spinal and corticospinal excitability of the lower limb muscles. However, little remains known on the involvement of somatosensory information in arm-leg neural interactions. Here, we investigated effects of voluntary and electrically induced wrist flexion on corticospinal excitability and somatosensory information processing of the lower limbs. In Experiment 1, we measured transcranial magnetic stimulation (TMS)-evoked motor evoked potentials (MEPs) of the resting soleus (SOL) muscle at rest or during voluntary or neuromuscular electrical stimulation (NMES)-induced wrist flexion. The wrist flexion force was matched to 10% of the maximum voluntary contraction (MVC). We found that SOL MEPs were significantly increased during voluntary, but not NMES-induced, wrist flexion, compared to the rest (P < .001). In Experiment 2, we examined somatosensory evoked potentials (SEPs) following tibial nerve stimulation under the same conditions. The results showed that SEPs were unchanged during both voluntary and NMES-induced wrist flexion. In Experiment 3, we examined the modulation of SEPs during 10%, 20% and 30% MVC voluntary wrist flexion. During 30% MVC voluntary wrist flexion, P50-N70 SEP component was significantly attenuated compared to the rest (P = .003). Our results propose that the somatosensory information generated by NMES-induced upper limb muscle contractions may have a limited effect on corticospinal excitability and somatosensory information processing of the lower limbs. However, voluntary wrist flexion modulated corticospinal excitability and somatosensory information processing of the lower limbs via motor areas.

A motion-induced position shift that depends on motion both before and after the test probe.

Two versions of the flash grab illusion were used to examine the relative contributions of motion before and motion after the test flash to the illusory position shift. The stimulus in the first two experiments was a square pattern that expanded and contracted with an outline square flashed each time the motion reversed producing a dramatic difference in perceived size between the two reversals. Experiment 1 showed a strong illusion when motion was present before and after the flashed tests or just after the flashes, but no significant effect when only the pre-flash motion was present. In Experiment 2, motion always followed the flash, and the duration of the pre-flash motion was varied. The results showed a significant increase in illusion strength with the duration of pre-flash motion and the effect of the pre-flash motion was almost 50% that of the post-flash motion. Finally, Experiment 3 tested the position shifts when the linear motion of a disk before the flash was orthogonal to its motion after the flash. Here, the results again showed that the pre-flash motion made a significant contribution, about 32% that of the post-flash motion. Several models are considered and even though all fail to some degree, they do offer insights into the nature of the illusion. Finally, we show that the empirical measure of the relative contribution of motion before and after the flash can be used to distinguish the mechanisms underlying different illusions.

Relationships between autistic traits, taste preference, taste perception, and eating behaviour.

Individuals with autism spectrum disorder exhibit atypical taste perception and eating behaviours. However, little is known about the effect of autistic traits on eating behaviours in the general population. This study explored the relationships between autistic traits, taste preferences, taste perceptions, and eating behaviours among Japanese population using an online questionnaire survey. The results showed significant effect of autistic traits on eating behaviours, that people with higher autistic traits tended to have higher selective eating behaviours, such as increased sensitivity to food texture and mixed flavours. Moreover, selective eating behaviours were correlated with the preference for sour taste and aftertaste sensitivity. Those results suggest that eating behaviours can be influenced by the relationship between autistic traits, taste perceptions, and taste preferences. We discuss these results in the context of previous findings, and future investigations into the possibility of solving selective eating problems in individuals with autism.

Phase dependent modulation of cortical activity during action observation and motor imagery of walking: An EEG study.

Action observation (AO) and motor imagery (MI) are motor simulations which induce cortical activity related to execution of observed and imagined movements. Neuroimaging studies have mainly investigated where the cortical activities during AO and MI of movements are activated and if they match those activated during execution of the movements. However, it remains unclear how cortical activity is modulated; in particular, whether activity depends on observed or imagined phases of movements. We have previously examined the neural mechanisms underlying AO and MI of walking, focusing on the combined effect of AO with MI (AO+MI) and phase dependent modulation of corticospinal and spinal reflex excitability. Here, as a continuation of our previous studies, we investigated cortical activity depending on gait phases during AO and AO+MI of walking by using electroencephalography (EEG); 64-channel EEG signals were recorded in which participants observed walking with or without imagining it, respectively. EEG source and spectral analyses showed that, in the sensorimotor cortex during AO+MI and AO, the alpha and beta power were decreased, and power spectral modulations depended on walking phases. The phase dependent modulations during AO+MI, but not during AO, were like those which occur during actual walking as reported by previous walking studies. These results suggest that combinatory effects of AO+MI could induce parts of the phase dependent activation of the sensorimotor cortex during walking even without any movements. These findings would extend understanding of the neural mechanisms underlying walking and cognitive motor processes and provide clinically beneficial information towards rehabilitation for patients with neurological gait dysfunctions.

Gait-phase-dependent and gait-phase-independent cortical activity across multiple regions involved in voluntary gait modifications in humans.

Modification of ongoing walking movement to fit changes in external environments requires accurate voluntary control. In cats, the motor and posterior parietal cortices have crucial roles for precisely adjusting limb trajectory during walking. In human walking, however, it remains unclear which cortical information contributes to voluntary gait modification. In this study, we investigated cortical activity changes associated with visually guided precision stepping using electroencephalography source analysis. Our results demonstrated frequency- and gait-event-dependent changes in the cortical power spectrum elicited by voluntary gait modification. The main differences between normal walking and precision stepping were as follows: (a) the alpha, beta or gamma power decrease during the swing phases in the sensorimotor, anterior cingulate and parieto-occipital cortices, and (b) a power decrease in the theta, alpha and beta bands and increase in the gamma band throughout the gait cycle in the parieto-occipital cortex. Based on the previous knowledge of brain functions, the former change was considered to be related to execution and planning of leg movement, while the latter change was considered to be related to multisensory integration and motor awareness. Therefore, our results suggest that the gait modification is achieved by higher cortical involvements associated with different sensorimotor-related functions across multiple cortical regions including the sensorimotor, anterior cingulate and parieto-occipital cortices. The results imply the critical importance of the cortical contribution to voluntary modification in human locomotion. Further, the observed cortical information related to voluntary gait modification would contribute to developing volitional control systems of brain-machine interfaces for walking rehabilitation.

Immediate action effects motivate actions based on the stimulus-response relationship.

The theory of event coding, an influential framework for action planning, suggests that humans first integrate stimulus, response, and action effect into representation (an event file) via their contingencies, and then, the activation of expected action effects drives the associated response. While previous studies have typically examined such functions of action effects after, rather than before or during, the acquirement of the representation, Eitam et al. (Exp Brain Res 229:475-484, 2013a) demonstrated that the presence of immediate feedback to action (i.e., action effects) can instantly elicit faster responses than delayed feedback. However, the underlying mechanism of this faciliatory effect remains unclear. Specifically, while the response-effect relationship has been highlighted, the role of stimuli has not been investigated. To address this issue, the present study conducted four experiments. We first reproduced the faciliatory effects of immediate action effects with between- and within-participants design (Experiments 1 and 2, respectively). Then, we assessed whether immediate action effects facilitate response speed, when stimuli (Experiment 3) and a combination of stimuli and responses (Experiment 4) determined the delay of action effects. The identical response was executed faster when driven by stimuli associated with immediate effects than by those associated with lagged effects. This result indicates that immediate action effects do not reinforce the execution of specific motor actions itself, but facilitate actions depending on the stimulus-response relationship. We discuss the potential mechanism of the facilitation effect.

Precise force controls enhance loudness discrimination of self-generated sound.

Motor executions alter sensory processes. Studies have shown that loudness perception changes when a sound is generated by active movement. However, it is still unknown where and how the motor-related changes in loudness perception depend on the task demand of motor execution. We examined whether different levels of precision demands in motor control affects loudness perception. We carried out a loudness discrimination test, in which the sound stimulus was produced in conjunction with the force generation task. We tested three target force amplitude levels. The force target was presented on a monitor as a fixed visual target. The generated force was also presented on the same monitor as a movement of the visual cursor. Participants adjusted their force amplitude in a predetermined range without overshooting using these visual targets and moving cursor. In the control condition, the sound and visual stimuli were generated externally (without a force generation task). We found that the discrimination performance was significantly improved when the sound was produced by the force generation task compared to the control condition, in which the sound was produced externally, although we did not find that this improvement in discrimination performance changed depending on the different target force amplitude levels. The results suggest that the demand for precise control to produce a fixed amount of force may be key to obtaining the facilitatory effect of motor execution in auditory processes.

People have modest, not good, insight into their face recognition ability: a comparison between self-report questionnaires.

Whether people have insight into their face recognition ability has been intensely debated in recent studies using self-report measures. Although some studies showed people's good insight, other studies found the opposite. The discrepancy might be caused by the difference in the questionnaire used and/or the bias induced using an extreme group such as suspected prosopagnosics. To resolve this issue, we examined the relationship between the two representative self-report face recognition questionnaires (Survey, N = 855) and then the extent to which the questionnaires differ in their relationship with face recognition performance (Experiment, N = 180) in normal populations, which do not include predetermined extreme groups. We found a very strong correlation (r = 0.82), a dominant principal component (explains > 90% of the variance), and comparable reliability between the questionnaires. Although these results suggest a strong common factor underlying them, the residual variance is not negligible (33%). Indeed, the follow-up experiment showed that both questionnaires have significant but moderate correlations with actual face recognition performance, and that the correlation was stronger for the Kennerknecht's questionnaire (r = - 0.38) than for the PI20 (r = - 0.23). These findings not only suggest people's modest insight into their face recognition ability, but also urge researchers and clinicians to carefully assess whether a questionnaire is suitable for estimating an individual's face recognition ability.

Dynamic presentation boosts the Ebbinghaus illusion but reduces the Müller-Lyer and orientation contrast illusions.

Mruczek et al. (2015) showed that a moving version of the Ebbinghaus illusion almost doubles in strength compared to the standard version. In their stimulus, the size of the surrounding inducers was modulated between large and small and the whole stimulus was made to drift during the surround modulation. We first replicated the original dynamic Ebbinghaus illusion and then explored dynamic presentations for other simultaneous contrast and geometric illusions. We found no increase in illusion strength in any that we sampled. Here we report the results for the Müller-Lyer illusion and the orientation contrast illusion. Surprisingly, when these two illusions were presented dynamically, their effects were greatly reduced for the Müller-Lyer illusion and eliminated for the orientation contrast illusion.

Rapid saccadic categorization of other-race faces.

The human visual system is very fast and efficient at extracting socially relevant information from faces. Visual studies employing foveated faces have consistently reported faster categorization by race response times for other-race compared with same-race faces. However, in everyday life we typically encounter faces outside the foveated visual field. In study 1, we explored whether and how race is categorized extrafoveally in same- and other-race faces normalized for low-level properties by tracking eye movements of Western Caucasian and East Asian observers in a saccadic response task. The results show that not only are people sensitive to race in faces presented outside of central vision, but the speed advantage in categorizing other-race faces occurs astonishingly quickly in as little as 200 ms. Critically, this visual categorization process was approximately 300 ms faster than the typical button press responses on centrally presented foveated faces. Study 2 investigated the genesis of the extrafoveal saccadic response speed advantage by comparing the influences of the response modality (button presses and saccadic responses), as well as the potential contribution of the impoverished low-spatial frequency spectrum characterizing extrafoveal visual information processing. Button press race categorization was not significantly faster with reconstructed retinal-filtered low spatial frequency faces, regardless of the visual field presentation. The speed of race categorization was significantly boosted only by extrafoveal saccades and not centrally foveated faces. Race is a potent, rapid, and effective visual signal transmitted by faces used for the categorization of ingroup/outgroup members. This fast universal visual categorization can occur outside central vision, igniting a cascade of social processes.

Source memory and social exchange in young children.

Reciprocal interactions require memories of social exchanges; however, little is known about how we remember social partner actions, especially during childhood when we start forming peer-to-peer relationships. This study examined if the expectation-violation effect, which has been observed in adults' source memory, exists among 5-6-year-old children. Forty participants played a coin collection game where they either received or lost coins after being shown an individual with a smiling or angry expression. This set-up generated congruent (smiling-giver and angry-taker) versus incongruent (smiling-taker and angry-giver) conditions. In the subsequent tasks, the children were asked to recall which actions accompanied each individual. The children considered the person with incongruent conditions as being stranger than the person with congruent conditions, suggesting that the former violated the children's emotion-based expectations. However, no heightened source memory was found for the incongruent condition. Instead, children seem to better recognise the action of angry individuals than smiling individuals, suggesting that angry facial expressions are more salient for children's source memory in a social exchange.

Neural correlates of online cooperation during joint force production.

During joint action, two or more persons depend on each other to accomplish a goal. This mutual recursion, or circular dependency, is one of the characteristics of cooperation. To evaluate the neural substrates of cooperation, we conducted a hyperscanning functional MRI study in which 19 dyads performed a joint force-production task. The goal of the task was to match their average grip forces to the target value (20% of their maximum grip forces) through visual feedback over a 30-s period; the task required taking into account other-produced force to regulate the self-generated one in real time, which represented cooperation. Time-series data of the dyad's exerted grip forces were recorded, and the noise contribution ratio (NCR), a measure of influence from the partner, was computed using a multivariate autoregressive model to identify the degree to which each participant's grip force was explained by that of their partner's, i.e., the degree of cooperation. Compared with the single force-production task, the joint task enhanced the NCR and activated the mentalizing system, including the medial prefrontal cortex, precuneus, and bilateral posterior subdivision of the temporoparietal junction (TPJ). In addition, specific activation of the anterior subdivision of the right TPJ significantly and positively correlated with the NCR across participants during the joint task. The effective connectivity of the anterior to posterior TPJ was upregulated when participants coordinated their grip forces. Finally, the joint task enhanced cross-brain functional connectivity of the right anterior TPJ, indicating shared attention toward the temporal patterns of the motor output of the partner. Since the posterior TPJ is part of the mentalizing system for tracking the intention of perceived agents, our findings indicate that cooperation, i.e., the degree of adjustment of individual motor output depending on that of the partner, is mediated by the interconnected subdivisions of the right TPJ.

Smiling enemies: Young children better recall mean individuals who smile.

Remembering whether a person is cooperative is essential in social interactions. It has been shown that adults have better memory of a person who showed an incongruence between emotional expression and expected behavior (e.g., smiling while stealing). To examine whether children would show similar emotional incongruity effects, we examined 70 children aged 5 or 6 years. They obtained coins that could be exchanged later for rewards (stickers) by answering quiz questions. Then, they participated in the coin collection game where individual persons with smiling or angry expressions appeared one at a time on a computer monitor. These same individuals then either gave coins to or took coins away from the children, leading to congruent (smiling giver and angry taker) and incongruent (smiling taker and angry giver) conditions. After the game, children needed to choose between two faces to indicate which one previously appeared in the game. Participants recognized faces better under the incongruent conditions. In particular, the smiling taker was recognized significantly better than the angry taker, whereas no difference was observed for the smiling and angry givers. Evidently, 5- and 6-year-olds better remember individuals whose facial expression or appearance is incongruent with their expected behavior.

Covert digital manipulation of vocal emotion alter speakers' emotional states in a congruent direction.

Research has shown that people often exert control over their emotions. By modulating expressions, reappraising feelings, and redirecting attention, they can regulate their emotional experience. These findings have contributed to a blurring of the traditional boundaries between cognitive and emotional processes, and it has been suggested that emotional signals are produced in a goal-directed way and monitored for errors like other intentional actions. However, this interesting possibility has never been experimentally tested. To this end, we created a digital audio platform to covertly modify the emotional tone of participants' voices while they talked in the direction of happiness, sadness, or fear. The result showed that the audio transformations were being perceived as natural examples of the intended emotions, but the great majority of the participants, nevertheless, remained unaware that their own voices were being manipulated. This finding indicates that people are not continuously monitoring their own voice to make sure that it meets a predetermined emotional target. Instead, as a consequence of listening to their altered voices, the emotional state of the participants changed in congruence with the emotion portrayed, which was measured by both self-report and skin conductance level. This change is the first evidence, to our knowledge, of peripheral feedback effects on emotional experience in the auditory domain. As such, our result reinforces the wider framework of self-perception theory: that we often use the same inferential strategies to understand ourselves as those that we use to understand others.

Nano Precipitation and Hardening of Die-Quenched 6061 Aluminum Alloy.

Die quenching is applied to an age-hardenable aluminium alloys to obtain super-saturated solid solution. The application is advantageous because it can reduce number of manufacturing processes, and may increase strength by strain aging. If die quenching is realized in forging as well as sheet forming, it may widen industrial applicability further. In this study, Al-Mg-Si alloy AA6061 8 mm-thick billets were reduced 50% in height without cracks by die-quench forging. Supersaturated solid solution was successfully obtained. The die-quenched specimen shows higher hardness with nano precipitates at shorter aging time than the conventional water-quenched specimen.

Gaze-Cueing With Crossed Eyes: Asymmetry Between Nasal and Temporal Shifts.

A person's direction of gaze (and visual attention) can be inferred from the direction of the parallel shift of the eyes. However, the direction of gaze is ambiguous when there is a misalignment between the eyes. The use of schematic drawings of faces in a previous study demonstrated that gaze-cueing was equally effective, even when one eye looked straight and the other eye was averted. In the current study, we used more realistic computer-generated face models to re-examine if the diverging direction of the eyes affected gaze-cueing. The condition where one eye was averted nasally while the other looked straight produced a significantly smaller gaze-cueing effect in comparison with when both eyes were averted in parallel or one eye was averted temporally. The difference in the gaze-cueing effect disappeared when the position of one eye was occluded with a rectangular surface or an eye-patch. These results highlight the possibility that the gaze-cueing effect might be weakened when a direct gaze exists between the cueing eye (i.e., nasally oriented eye) and the target and the effect magnitude might depend on which type of face stimulus are used as a cue.

Contribution of global and local biological motion information to speed perception and discrimination.

To respond to movements of others and understand the intention of others' actions, it is important to accurately extract motion information from body movements. Here, using original and spatially scrambled point-light biological motions in upright and inverted orientations, we investigated the effect of global and local biological motion information on speed perception and sensitivity. The speed discrimination task revealed that speed sensitivity was higher for the original than for scrambled stimuli (Experiment 1) and higher for upright than for inverted stimuli (Experiment 2). Perceived motion speed was slower for the original than for scrambled stimuli (Experiment 2), but regardless of the orientation of the display (Experiment 1). A subsequent experiment comparing different scrambled stimuli of the same actions showed that the higher speed discrimination sensitivity to upright stimuli was preserved even in the scrambled biological motions (Experiment 3). Taken together, our findings suggest that perception of the speed of biological movements emanates from both global and local biological motion signals.