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	<title>social attention &#8211; Science</title>
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	<title>social attention &#8211; Science</title>
	<link>https://scienmag.com</link>
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		<title>Up Is Not Down: Head Movements Pull Attention in Opposite Directions Depending on Axis</title>
		<link>https://scienmag.com/up-is-not-down-head-movements-pull-attention-in-opposite-directions-depending-on-axis/</link>
		
		<dc:creator><![CDATA[Glenn Wilkins]]></dc:creator>
		<pubDate>Tue, 13 Oct 2026 23:11:40 +0000</pubDate>
				<category><![CDATA[Psychology & Psychiatry]]></category>
		<category><![CDATA[anticipatory inference]]></category>
		<category><![CDATA[attentional orienting]]></category>
		<category><![CDATA[but this study questions that assumption by exploring vertical versus horizontal head and gaze cues.]]></category>
		<category><![CDATA[dimensional asymmetry]]></category>
		<category><![CDATA[eye-head coordination]]></category>
		<category><![CDATA[gaze perception]]></category>
		<category><![CDATA[gaze-head integration]]></category>
		<category><![CDATA[head movements]]></category>
		<category><![CDATA[joint attention]]></category>
		<category><![CDATA[overshoot effect]]></category>
		<category><![CDATA[psychophysics]]></category>
		<category><![CDATA[regardless of head orientation]]></category>
		<category><![CDATA[social attention]]></category>
		<category><![CDATA[social attention primarily driven by eye movements]]></category>
		<category><![CDATA[spatial cueing]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=269331</guid>

					<description><![CDATA[New experiments show that attention follows vertically tilting heads but moves opposite to horizontally turning heads, revealing a dimensional asymmetry in how the brain integrates gaze and head cues.]]></description>
										<content:encoded><![CDATA[<p>When someone turns their head to the left while keeping their eyes locked on you, your attention does something strange: it drifts in the opposite direction. This counterintuitive phenomenon, known as the overshoot effect, has fascinated vision scientists for decades. Now a new study suggests that this quirk of social attention is not a universal rule of the human brain but a peculiarity of horizontal space. When heads tilt up or down instead of turning left or right, attention follows the head rather than fleeing from it. The finding, published in the journal Attention, Perception, &amp; Psychophysics, reveals a striking dimensional asymmetry in how the mind reads the attention of others, and it challenges long-standing theories of how gaze and head cues are combined.</p>
<p>The research, conducted by Felix J. Götz, Paul M. Heineck, Anne Böckler, and Andreas B. Eder at the Julius-Maximilians-University of Würzburg, set out to answer a deceptively simple question: does the brain integrate gaze and head information the same way in vertical space as it does in horizontal space? The dominant models of social attention, developed largely to explain horizontal effects, implicitly assume that it does. Hierarchical accounts propose that the eyes are the privileged signal, with head orientation playing a subordinate role. Holistic accounts instead argue that gaze, head, and body cues are merged in parallel into a single estimate of where another person is looking. Both frameworks predict that a misaligned configuration, in which the head points one way and the eyes another, should produce similar attentional consequences regardless of whether the misalignment occurs along the horizontal or the vertical axis.</p>
<p>The Würzburg team suspected otherwise, and their reasoning drew on the biomechanics of real eye-head coordination. In everyday life, people glance left and right with ease while keeping the head nearly still, but looking up or down typically requires a tighter coupling of eyes and head, because vertical eye mobility is comparatively restricted. Misalignments between eye and head direction therefore occur far more often along the horizontal axis than the vertical one. If the visual system has internalized these ecological regularities, it should treat a vertically tilted head as a more reliable predictor of where attention is heading, while in the horizontal plane it may lean more heavily on gaze information and anticipate how the eyes will move next. To test this, the researchers needed stimuli in which the head itself visibly moved, rather than the static photographs used in most classic overshoot experiments.</p>
<p>Across four preregistered experiments, participants viewed centrally presented faces of four models wearing uniform black shirts against a white background. Each trial began with a fixation cross, followed by a neutral head image for one second. The image was then replaced by a shifted version: the head turned left or right, or tilted up or down. After 300 milliseconds, a blue circle or square appeared at one of two locations on the relevant axis, and participants classified its shape as quickly as possible. Crucially, the cues were entirely non-predictive; targets were equally likely to appear at cued and uncued locations, so any response-time differences reflected spontaneous shifts of attention rather than learned expectancies. Gaze visibility was manipulated between experiments, with the models either gazing directly at the observer or keeping their eyes closed.</p>
<p>The first two experiments probed the vertical dimension. In Experiment 1, with direct gaze maintained throughout, forty-three participants identified targets significantly faster when the target location matched the direction of the head tilt, a head-congruency effect of roughly twelve milliseconds, with an effect size of dz = 0.67. Attention, in other words, followed the head upward or downward rather than overshooting away from it. But a rival explanation remained: the vertical tilt also displaced the eye region toward the target, so the effect might have been driven by the position of the eyes rather than the head itself. Experiment 2 eliminated this confound by repeating the procedure with closed eyes. The head-congruency effect not only persisted but grew dramatically stronger, reaching dz = 1.60, with targets at head-congruent locations detected about seventeen milliseconds faster. Vertical cueing, the authors concluded, genuinely reflects head orientation, not displaced eye position.</p>
<p>Experiments 3 and 4 then turned to the horizontal axis, and here the classic pattern re-emerged in unexpected form. With direct gaze and dynamic head turns, Experiment 3 replicated the overshoot effect: participants responded faster to targets appearing opposite to the head direction, with a significant effect of dz = 0.65. This confirmed that the overshoot survives the transition from static images to moving heads. The surprise came in Experiment 4, where the researchers removed all gaze information by closing the models&#8217; eyes. Standard cue-weighting logic predicted that without eyes to compete with, head orientation should dominate and the overshoot should reverse into head-following. Instead, the opposite happened. The head-opposite bias grew even stronger, reaching dz = 0.92, with head-incongruent targets identified about thirteen milliseconds faster. Attention fled from the direction of the head turn even when there were no eyes to read at all.</p>
<p>Exploratory comparisons across the four experiments reinforced the dimensional dissociation. Pooling the vertical experiments, the head-congruency effect was significantly larger with eyes closed than with eyes open, an interaction confirmed by linear mixed models fitted to log-transformed single-trial response times. The same pattern appeared horizontally, where the overshoot-like bias was modestly amplified without visible gaze, though the authors flag this horizontal modulation as tentative given its smaller size and exploratory status. Taken together, the results suggest that direct gaze acts as an additional attentional signal that attenuates head-based cueing in both dimensions, but that it never changes the direction of the effect. Vertical attention follows heads; horizontal attention flees them, with or without eyes.</p>
<p>What could produce such a bizarre horizontal bias in the complete absence of gaze? The authors propose that observers do not merely encode the current geometric relationship between eyes and head but engage in anticipatory inference about how another person&#8217;s attention will be realigned. A dynamically turning head implies that attention is in transit. In the vertical dimension, where eye and head movements are tightly coupled, the head is a trustworthy forecast of where the person will look, so observers orient toward it. In the horizontal dimension, where the eyes roam independently, a turning head may signal that the person is disengaging from one location and redirecting attention elsewhere, prompting observers to orient toward the likely source of that shift. Removing gaze information may increase the ambiguity of the observed movement, encouraging richer, intention-based interpretations, such as avoidance or disengagement, rather than simple directional reading. This account aligns with the idea of attention reading, in which observers dynamically integrate head, gaze, and motion cues to predict where someone&#8217;s attention will land next.</p>
<p>The findings are difficult to reconcile with strictly hierarchical models, which cannot explain head-following in the vertical dimension, or with holistic models, which predict no dimensional asymmetries at all and certainly cannot accommodate a horizontal head-opposite bias when no gaze is visible. Instead, they favor flexible, predictive frameworks in which cue integration is constrained by the biomechanics and ecology of eye-head coordination. The authors acknowledge limitations: response times offer only an indirect window onto attention compared with eye tracking, the stimulus set comprised just four models, and the horizontal and vertical manipulations were run in separate experiments for methodological reasons. Yet the consistency of the dissociation across four preregistered studies, with all materials and data publicly available on the Open Science Framework, makes a compelling case. The next time a friend tilts their chin toward the ceiling, your attention will dutifully follow. But should they swing their head to the side while their eyes stay on you, your mind, ever the fortune-teller, will already be looking where they are about to look next.</p>
<p><strong>Subject of Research:</strong> Dimensional asymmetries in social attention and gaze-head cue integration during dynamic head movements</p>
<p><strong>Article Title:</strong> Dimensional asymmetries in social attention: Dynamic head movements elicit opposite attentional biases in vertical versus horizontal dimensions</p>
<p><strong>Article References:</strong> Götz, F. J., Heineck, P. M., Böckler, A., &amp; Eder, A. B. (2026). Dimensional asymmetries in social attention: Dynamic head movements elicit opposite attentional biases in vertical versus horizontal dimensions. <em>Attention, Perception, &amp;amp; Psychophysics, 88</em>(7), Article 205. <a href="https://doi.org/10.3758/s13414-026-03351-3" rel="noopener noreferrer">https://doi.org/10.3758/s13414-026-03351-3</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.3758/s13414-026-03351-3" rel="noopener noreferrer">10.3758/s13414-026-03351-3</a></p>
<p><strong>Keywords:</strong> social attention, gaze-head integration, overshoot effect, spatial cueing, head movements, eye-head coordination, joint attention, anticipatory inference, gaze perception, attentional orienting, dimensional asymmetry, psychophysics</p>
]]></content:encoded>
					
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">269331</post-id>	</item>
		<item>
		<title>Newborns Show Sex Differences in Attention Within Hours of Birth, Cambridge Study Finds</title>
		<link>https://scienmag.com/newborns-show-sex-differences-in-attention-within-hours-of-birth-cambridge-study-finds/</link>
		
		<dc:creator><![CDATA[Harold Sullivan]]></dc:creator>
		<pubDate>Mon, 12 Oct 2026 08:15:49 +0000</pubDate>
				<category><![CDATA[Social Science]]></category>
		<category><![CDATA[autism]]></category>
		<category><![CDATA[Autism Research Centre]]></category>
		<category><![CDATA[biological influences on infant development]]></category>
		<category><![CDATA[biological versus social origins of gender traits]]></category>
		<category><![CDATA[Biology of Sex Differences]]></category>
		<category><![CDATA[Cambridge infant study]]></category>
		<category><![CDATA[early behavioral differences between boys and girls]]></category>
		<category><![CDATA[early sex differences in cognition]]></category>
		<category><![CDATA[face preference]]></category>
		<category><![CDATA[hormones]]></category>
		<category><![CDATA[infant attention differences]]></category>
		<category><![CDATA[infant attention within hours of birth]]></category>
		<category><![CDATA[infant gaze]]></category>
		<category><![CDATA[infant visual preferences]]></category>
		<category><![CDATA[nature and nurture]]></category>
		<category><![CDATA[newborn gender behavior]]></category>
		<category><![CDATA[newborn infants]]></category>
		<category><![CDATA[newborn social attention]]></category>
		<category><![CDATA[prenatal factors]]></category>
		<category><![CDATA[sex differences]]></category>
		<category><![CDATA[sex differences in early infancy]]></category>
		<category><![CDATA[social attention]]></category>
		<category><![CDATA[social vs non-social stimuli in infants]]></category>
		<category><![CDATA[University of Cambridge]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=264106</guid>

					<description><![CDATA[Cambridge researchers report that newborn girls and boys differ on average in attention to faces versus objects within hours of birth, suggesting prenatal biological factors contribute alongside later experience.]]></description>
										<content:encoded><![CDATA[<p>One of the longest-running debates in psychology concerns the origins of differences between men and women in behaviour, cognition and social development. Are these differences learned, absorbed from a culture that treats boys and girls differently from the moment they are born, or do they partly reflect biological factors that operate before a child has any experience of the social world at all? A new study from the University of Cambridge offers what its authors describe as a unusually direct way into that question, because it examines infants just hours after birth, an age at which postnatal socialisation has barely begun.</p>
<p>The research, published in the journal Biology of Sex Differences, tested 130 newborn infants, each examined only hours after delivery. The team, based at the University&#8217;s Autism Research Centre, presented the babies with two videos shown side by side. One was a social stimulus: a human face moving naturally. The other was a non-social stimulus: a Newton&#8217;s cradle, the familiar desk toy in which a row of metallic balls swings under gravity and their mechanical properties, transferring momentum from one end of the row to the other. Neither stimulus carried cultural meaning; one simply depicted a person, the other depicted moving objects.</p>
<p>The central finding was that, regardless of sex, newborn infants generally preferred to look at the social stimulus. Human faces, it seems, exert a powerful pull on attention from the very start of life. But when the researchers compared the two sexes, a consistent on-average difference emerged. Female infants spent a greater proportion of their looking time on the face, while male infants spent a greater proportion of their time on the swinging balls. The effect is a difference in averages between groups, not a categorical split, and the researchers are explicit that there is substantial variation within each sex and considerable overlap between them.</p>
<p>The result matters because of its timing. Within hours of birth, an infant has had almost no exposure to gendered clothing, toys, parental expectations or any of the countless cultural signals that shape development in the months and years that follow. If differences in social attention are already measurable at this point, the authors argue, then prenatal biological factors that differ between the sexes during pregnancy, such as sex hormone levels and genetic influences, are likely to contribute to them. That does not mean biology determines everything; rather, it suggests that prenatal factors set up early tendencies that later interact with experience.</p>
<p>The study is, in an important sense, a replication. In 2000, researchers at the University of Cambridge published a study reporting that newborn girls, on average, looked longer at faces while newborn boys, on average, looked longer at objects. That finding was influential but also contested, and scientists in the field called for it to be repeated under more rigorous conditions. Until now, no team had attempted it. The reason is practical as much as scientific: carrying out controlled experimental research on newborn infants is extraordinarily difficult. Recruitment must happen around unpredictable deliveries, testing windows are measured in hours, and every aspect of the procedure has to be gentle enough for babies only recently out of the womb.</p>
<p>The new study was designed to answer those methodological criticisms. Compared with the original 2000 experiment, it used more controlled experimental testing conditions and a more reliable method for monitoring infant gaze. Crucially, the researchers who analysed the videos of the babies&#8217; eyes were blind to two things: the sex of each baby, and whether the baby was looking at the social or the non-social stimulus. This double-blinding of the analysis stage ensured that the expectations of the people coding the data could not bias the results, a safeguard that addresses one of the most common sources of concern in observational infant research.</p>
<p>Yumnah Khan, a PhD student at the Autism Research Centre and the lead researcher on the study, placed the finding in the context of the lab&#8217;s broader research programme. Our recent research has also shown that on-average sex differences are present in brain structure at birth and emerge prenatally, she said. This new study tells us that there are not only on-average sex differences in the brain but also in attention and behaviour. In other words, the structural and the behavioural evidence now point in the same direction: some differences between the sexes are detectable before postnatal experience could plausibly have produced them.</p>
<p>Professor Sir Simon Baron-Cohen, Director of the Autism Research Centre, who supervised the study, framed the result as a contribution to one of psychology&#8217;s oldest arguments. This study addresses the age-old question of whether nature plays any role at all in shaping sex differences in the human mind and brain, he said. The fact that we observe these differences within hours of birth, before extensive postnatal experience has occurred, suggests that prenatal factors play a role, and that these prenatal factors, sex hormones and/or genes, go on to interact with postnatal experience. In other words, it&#8217;s nature and nurture, not nature or nurture. That formulation is a deliberate rejection of the binary framing that has often dominated public discussion of the topic, in which commentators are asked to choose between a fully biological and a fully cultural account.</p>
<p>Other members of the team emphasised the limits of what the study can claim. Dr Alex Tsompanidis, Assistant Research Professor at the Autism Research Centre, noted that sex differences at birth are important as starting points, but that they do not fully determine how children learn and develop in later life, because biological and social factors always interact, contributing to the rich diversity of human societies. Professor Carrie Allison, Deputy Director of the Centre, stressed the statistical character of the finding: the differences do not apply to all male or all female infants, and are only seen when groups are compared on average. Our future research needs to better understand that variation, she said, pointing to the overlap between the sexes as a key target for further work.</p>
<p>The team&#8217;s next step is a longitudinal follow-up study, already underway and funded by the K. Lisa Yang Centre for Autism Research at Cambridge, part of the Yang Tan Collective. By following the same children over time, the researchers hope to determine whether these earliest differences in attention contribute to later differences in children&#8217;s minds, brains and behaviour. The stakes extend beyond the nature-versus-nurture debate itself. Girls, on average, learn to talk earlier and develop social skills faster than boys, and conditions such as autism, which is diagnosed about twice as often in boys as in girls, may be connected to the same developmental pathways. The researchers hope that by understanding the origins of the earliest sex differences, scientists can better understand neurodiversity and the conditions in which it is expressed. The original study was supported by the Wellcome Trust, the Simon Foundation Autism Research Initiative and a PhD studentship from Trinity College, Cambridge and the Cambridge Trust.</p>
<p><strong>Subject of Research:</strong> Sex differences in newborn social attention and their prenatal origins</p>
<p><strong>Article Title:</strong> Sex differences in attention are present at birth, study finds</p>
<p><strong>Article References:</strong> Sex differences in attention are present at birth, study finds. (n.d.). <a href="https://www.eurekalert.org/news-releases/1144240" rel="noopener noreferrer">Original publication</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> Not provided</p>
<p><strong>Keywords:</strong> newborn infants, sex differences, social attention, prenatal factors, Autism Research Centre, University of Cambridge, Biology of Sex Differences, face preference, nature and nurture, infant gaze, autism, hormones</p>
]]></content:encoded>
					
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">264106</post-id>	</item>
		<item>
		<title>Babies&#8217; Gaze Between Eyes and Mouth Shifts With Speech Rhythm, Autism Family History and Language</title>
		<link>https://scienmag.com/babies-gaze-between-eyes-and-mouth-shifts-with-speech-rhythm-autism-family-history-and-language/</link>
		
		<dc:creator><![CDATA[Ophelia Keating]]></dc:creator>
		<pubDate>Wed, 07 Oct 2026 10:49:33 +0000</pubDate>
				<category><![CDATA[Medicine]]></category>
		<category><![CDATA[ADHD]]></category>
		<category><![CDATA[attention deficit hyperactivity disorder (ADHD) genetic factors]]></category>
		<category><![CDATA[autism]]></category>
		<category><![CDATA[Autism risk in infants]]></category>
		<category><![CDATA[developmental psychology]]></category>
		<category><![CDATA[developmental trajectory of face gaze]]></category>
		<category><![CDATA[early indicators of social communication difficulties]]></category>
		<category><![CDATA[early markers of autism]]></category>
		<category><![CDATA[eye tracking]]></category>
		<category><![CDATA[face perception in autism spectrum disorder]]></category>
		<category><![CDATA[face scanning]]></category>
		<category><![CDATA[family history]]></category>
		<category><![CDATA[gaze patterns between eyes and mouth]]></category>
		<category><![CDATA[impact of speech rhythm on infant gaze]]></category>
		<category><![CDATA[infancy]]></category>
		<category><![CDATA[infant face-scanning behavior]]></category>
		<category><![CDATA[influence of family history on autism development]]></category>
		<category><![CDATA[language development]]></category>
		<category><![CDATA[longitudinal study]]></category>
		<category><![CDATA[longitudinal study of infant attention]]></category>
		<category><![CDATA[social attention]]></category>
		<category><![CDATA[speech rhythm and social attention]]></category>
		<category><![CDATA[theta frequency]]></category>
		<category><![CDATA[visual attention]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=244117</guid>

					<description><![CDATA[A longitudinal eye-tracking study of 160 infants shows that attention to eyes versus mouths shifts with age, is modulated by speech-like movement frequencies, and is shaped by family history of autism and ADHD as well as emerging language skills.]]></description>
										<content:encoded><![CDATA[<p>Where do babies look when they watch a face? For decades, developmental scientists have debated whether infants at elevated genetic risk for autism scan faces differently from their peers, and the literature has produced a frustrating tangle of contradictory findings. A new longitudinal study, published in the Journal of Autism and Developmental Disorders, suggests that part of the confusion may come from two overlooked sources of variability: the speed at which a mouth moves, and the presence of attention deficit hyperactivity disorder (ADHD) in the family. By following 160 infants from five months to three years of age, the research team, led by Mary Agyapong of King&#8217;s College London together with colleagues at Birkbeck, University of London, has produced one of the most detailed pictures yet of how early face-scanning behaviour unfolds in children with and without a family history of autism or ADHD.</p>
<p>The study drew on the STAARS cohort, the Studying Autism and ADHD Risk in Siblings project, recruited through the Birkbeck Centre for Brain and Cognitive Development. Families were enrolled if they had a first-degree relative with a clinical diagnosis of autism, a clinical or probable research diagnosis of ADHD, or if they had typically developing older children and no first-degree relatives with either condition. The final sample comprised 79 infants with an elevated likelihood of autism, 31 with an elevated likelihood of ADHD, 21 with elevated likelihood of both conditions, and 29 with typical likelihood for neither. Each child visited the lab at five, ten and fourteen months for eye-tracking sessions, and returned for developmental and language assessments at 36 months, allowing the researchers to connect infant gaze patterns with later language outcomes.</p>
<p>The experimental task was elegantly simple. At each visit, infants watched pairs of ten-second silent videos of a woman&#8217;s face presented side by side on a screen. In each pair, the mouth flashed open and closed at one of three temporal frequencies: a slow one hertz, a mid-range six hertz, or a fast ten to fifteen hertz, depending on the age of the infant. The mid-frequency condition is scientifically crucial because fluent speech carries most of its energy in the theta band, roughly four to eight hertz, the rhythm at which syllables are produced. Neural oscillations in this theta range are thought to be central to how the brain segments and processes speech, and previous work has shown that even newborns show theta-frequency neural activity related to speech perception. The researchers wanted to know whether babies&#8217; eyes are drawn to mouths moving at this language-relevant rhythm.</p>
<p>Gaze was recorded with a Tobii TX-300 infrared eye tracker sampling at 120 hertz while infants sat on a parent&#8217;s lap. The team computed an eye-mouth looking index, or EMI, defined as the proportion of face-directed looking time spent on the eyes relative to the eyes plus the mouth combined. An index above 0.5 signals a preference for the eyes; below 0.5, a preference for the mouth. Trials with fewer than 25 percent valid gaze samples were discarded, and the longitudinal data were analysed with generalised linear mixed models, a statistical framework well suited to the missing data and bounded proportions that characterise infant eye-tracking studies.</p>
<p>The developmental pattern was clear. Across the whole sample, the eye-mouth index declined significantly between five and fourteen months, meaning that as babies grew older they shifted their attention progressively away from the eyes and toward the mouth. This replicates a well-established trajectory: typically developing infants look predominantly at the eyes before about five months of age and then increasingly favour the mouth through the first year, precisely the period during which they begin to comprehend and produce their first words. Interestingly, the researchers did not observe the re-orienting back toward the eyes around twelve months that some earlier studies reported, and they note that other work has found mouth attention persisting in both monolingual and bilingual children up to age five, supporting the idea that watching a moving mouth is adaptive for language learning.</p>
<p>Temporal frequency also mattered. Infants looked more at the eyes relative to the mouth when watching the slow one hertz faces than when watching the six hertz, speech-like faces. In other words, mouths moving at the rhythm of syllabic speech captured more attention than slowly moving mouths, providing partial behavioural support for the idea that human infants, like rhesus monkeys in earlier work by Asif Ghazanfar and colleagues, are perceptually tuned to theta-frequency facial movement. The effect was not exclusive, however: there was no significant difference in looking between the mid-frequency and high-frequency conditions, suggesting that the tuning is not a narrow bandpass filter but perhaps reflects a broader preference shaped by arousal and stimulus salience, which the authors flag as a target for future research measuring physiological arousal.</p>
<p>The most striking findings concerned family history. Infants with an elevated likelihood of autism showed a significantly larger eye-mouth index than infants with typical likelihood, meaning they looked relatively more at the eyes and less at the mouth across infancy. The authors interpret this as a possible developmental delay in the usual shift from eyes to mouth, since prolonged eye preference is normally a feature of younger infants. Crucially, this effect was attenuated when there was also a family history of ADHD: the interaction between autism and ADHD familial likelihood was significant, and at fourteen months the EL-autism group showed a larger index than the EL-autism-plus-ADHD group. A family history of ADHD on its own was also associated with more eye relative to mouth looking at fourteen months, a novel result in a population that has been almost entirely neglected by the eye-tracking literature. The authors argue that future family-history studies of autism should systematically map ADHD in the family, because its presence may mask or modify the effects researchers are trying to detect, potentially explaining some of the heterogeneity in previous reports.</p>
<p>Language added a further layer of nuance. At fourteen months, infants who had already said their first words, as measured by an item on the Mullen Scales of Early Learning, showed a smaller concurrent eye-mouth index, that is, more mouth looking, than infants who had not yet produced words, with a medium-to-large effect. This fits the experience-dependent view of face attention: once babies begin talking, watching mouth movements may help them refine and imitate the shapes of words they hear from speakers. Yet the long-term picture was more surprising. When the researchers controlled for fourteen-month word status, higher receptive language scores at 36 months were associated with greater looking to the eyes, not the mouth, across infancy. This ran counter to the authors&#8217; prediction and to some previous findings linking mouth preference to better later language. One interpretation, drawing on recent work by Viktorsson and colleagues, is that looking at the eyes supports gaze following and joint attention, which are themselves foundational for word learning. The takeaway, the authors suggest, is that both eyes and mouth matter: mouth looking serves emerging language skills in the moment, while eye engagement relates to the interpersonal foundations of language that come to fruition in toddlerhood.</p>
<p>Not every hypothesis was confirmed. There were no significant differences between likelihood groups in parent-reported comprehension or production vocabulary at fourteen months on the MacArthur-Bates Communicative Development Inventory, although girls comprehended significantly more words than boys, consistent with the broader literature on early sex differences in language. Nor did the frequency effect interact with word status, and neither expressive nor receptive language at 36 months related to infant EMI until first-word status was taken into account. The authors are candid about the limitations of their design. The silent videos isolated mouth movement in a way naturalistic speech does not, arousal was not measured, and the cohort, though prospective and well characterised, was underpowered to examine actual autism or ADHD diagnoses as outcomes. Causal conclusions are therefore off the table.</p>
<p>Even with those caveats, the study delivers a message that resonates well beyond specialist circles: the way a baby looks at a face is not a single fixed trait but a moving target shaped by age, by the rhythm of the face itself, by the constellation of conditions in the family, and by the child&#8217;s own blossoming language. For researchers hunting early markers of neurodevelopmental conditions, the implication is that heterogeneous findings may partly reflect unmeasured heterogeneity in the samples, particularly the under-appreciated role of familial ADHD. For parents, the study offers no cause for alarm but a fascinating window into the infant mind, revealing that from the earliest months, babies are already calibrating their gaze to the rhythms of human communication, sampling eyes and mouths in a dynamic balance that foreshadows the conversational partners they will one day become.</p>
<p><strong>Subject of Research:</strong> Infant eye-tracking study of visual attention to eyes versus mouths in relation to familial autism and ADHD likelihood and language development</p>
<p><strong>Article Title:</strong> Infant Attention to Eyes Versus Mouth Varies With Mouth Movement Speed, Family History of Autism and Language Development</p>
<p><strong>Article References:</strong> Agyapong, M., Mason, L., Begum Ali, J., Johnson, M. H., Charman, T., Jones, E. J. H., the STAARS Team, Bazelmans, T., Dafner, L., Ersoy, M., Gliga, T., Goodwin, A., Haartsen, R., Halkola, H., Hendry, A., Holman, R., Kalwarowsky, S., Kolesnik, A., Lloyd-Fox, S., &#8230; Taylor, C. (2026). Infant Attention to Eyes Versus Mouth Varies With Mouth Movement Speed, Family History of Autism and Language Development. <em>Journal of Autism and Developmental Disorders</em>. <a href="https://doi.org/10.1007/s10803-026-07516-9" rel="noopener noreferrer">https://doi.org/10.1007/s10803-026-07516-9</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1007/s10803-026-07516-9" rel="noopener noreferrer">10.1007/s10803-026-07516-9</a></p>
<p><strong>Keywords:</strong> autism, ADHD, infancy, eye-tracking, language development, visual attention, face scanning, theta frequency, family history, longitudinal study, social attention, developmental psychology</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">244117</post-id>	</item>
		<item>
		<title>Where We Look Next Depends on How Close a Face Gets</title>
		<link>https://scienmag.com/where-we-look-next-depends-on-how-close-a-face-gets/</link>
		
		<dc:creator><![CDATA[Glenn Wilkins]]></dc:creator>
		<pubDate>Sat, 12 Sep 2026 12:50:23 +0000</pubDate>
				<category><![CDATA[Psychology & Psychiatry]]></category>
		<category><![CDATA[approach and avoidance]]></category>
		<category><![CDATA[attention and reward mechanisms]]></category>
		<category><![CDATA[attentional bias]]></category>
		<category><![CDATA[dwell time]]></category>
		<category><![CDATA[experimental psychology on gaze and attention]]></category>
		<category><![CDATA[eye tracking]]></category>
		<category><![CDATA[face approach and recede effects]]></category>
		<category><![CDATA[face perception]]></category>
		<category><![CDATA[gaze allocation]]></category>
		<category><![CDATA[gaze-triggered feedback]]></category>
		<category><![CDATA[gaze-triggered social outcomes]]></category>
		<category><![CDATA[human attention]]></category>
		<category><![CDATA[influence of movement on visual attention]]></category>
		<category><![CDATA[interpersonal distance]]></category>
		<category><![CDATA[linear mixed-effects model]]></category>
		<category><![CDATA[motion perception and gaze behavior]]></category>
		<category><![CDATA[perception of approaching and receding faces]]></category>
		<category><![CDATA[social attention]]></category>
		<category><![CDATA[social cognition]]></category>
		<category><![CDATA[social cues in visual attention]]></category>
		<category><![CDATA[social gaze and facial movement]]></category>
		<category><![CDATA[social meaning and attention modulation]]></category>
		<category><![CDATA[value-driven attention]]></category>
		<category><![CDATA[value-driven attention and social cues]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=194471</guid>

					<description><![CDATA[A new eye-tracking study shows that when a person's gaze triggers a virtual face to approach, they later look less at that face, revealing that gaze-triggered interpersonal-distance outcomes can systematically reshape subsequent attentional allocation.]]></description>
										<content:encoded><![CDATA[<p>Human attention is not a passive camera. It is shaped by history, by reward, by social meaning, and—according to a new study—by the apparent movements of other people through the space between us. In a carefully controlled experiment published in Attention, Perception, &amp; Psychophysics, researchers at the University of Tsukuba in Japan found that when a participant&#8217;s gaze triggered a face to appear to approach, that same face later received less attention when it was shown again, motionless, on the screen. Faces that appeared to recede, by contrast, produced no reliable change in how they were subsequently viewed. The finding is subtle but consequential: it suggests that gaze itself can act as a trigger for social outcomes that later reshape where we direct our eyes, and that the direction of that reshaping is not what a simple reward-learning account might predict.</p>
<p>The study, led by Canling An of the Doctoral Program in Psychology at the University of Tsukuba together with Soichiro Matsuda of the university&#8217;s Institute of Human Sciences, tackled a question that sits at the intersection of two established research traditions. The first concerns value-driven attention: a large body of work has shown that stimuli previously associated with reward continue to capture attention even when they are no longer relevant to the task at hand. Faces associated with social reward, monetary outcomes, and emotional expressions can all bias visual selection in lasting ways. The second tradition concerns interpersonal distance, a fundamental dimension of social perception. Approaching stimuli are oriented to faster, and stimuli in near, peripersonal space measurably alter neural markers of attentional engagement. What had remained unclear was whether repeated exposure to distance-related social outcomes—someone seeming to come closer or move away in response to being looked at—would leave a measurable trace in later patterns of gaze allocation.</p>
<p>To answer that question, the researchers designed an experiment that carefully disentangles the initiating role of gaze from the ongoing experience of watching a stimulus change. Fifty adults, all students at the University of Tsukuba with normal or corrected-to-normal vision, completed two experimental blocks in a within-subjects design: one Approach block and one Recede block. Each block contained a Baseline phase, a Training phase, and a Test phase. In the Baseline and Test phases, participants simply viewed two static neutral female faces drawn from the AIST Facial Expression Database, each measuring roughly 9.75 degrees of visual angle and displayed on either side of, or above and below, a central fixation point. The dependent variable was the proportion of total dwell time directed at whichever face had been designated the gaze-triggered face in that block.</p>
<p>The Training phase was where the manipulation lived. Participants viewed a single face on each trial, and if they fixated on the gaze-triggered face for 300 milliseconds, a two-second animation was launched. Crucially, once triggered, the animation proceeded independently of any further gaze behavior. In the Approach condition, the face grew to approximately 635 by 635 pixels—a simulated advance toward the observer, from an estimated apparent distance of roughly 110–130 centimeters down to about 70–85 centimeters. In the Recede condition, the face shrank to roughly 152 by 152 pixels, corresponding to an apparent withdrawal to around 300–360 centimeters. The static comparison face remained unchanged for the same duration. Because the animation ran on its own after the 300-millisecond trigger threshold was met, the design avoided the continuous gaze–stimulus coupling of classic gaze-contingent paradigms and instead captured a discrete, everyday feature of social interaction: sustained gaze can mark a transition point after which interpersonal events unfold without depending moment to moment on where the eyes go next.</p>
<p>The technical execution reflected considerable methodological care. Eye movements were recorded with a Tobii X3-120 screen-based tracker sampling at 120 Hz, with calibration accuracy required to be below one degree of visual angle before testing. Each block consisted of four baseline trials, forty-eight training trials—twenty-four with the gaze-triggered face and twenty-four with the static face in randomized order—and four test trials. Baseline and test trial counts were deliberately kept low to limit fatigue and minimize additional exposure that might itself alter gaze patterns. Participants received no verbal instructions and were never told about the contingencies linking their gaze to the animations. Condition order and the assignment of face identities to the gaze-triggered role were counterbalanced across participants. After the experiment, participants completed the Japanese version of the Autism-Spectrum Quotient, whose scores served as an individual-difference measure given prior evidence linking autistic traits to variation in gaze behavior.</p>
<p>The analysis centered on dwell-time proportion—the fraction of dwell time on the gaze-triggered face relative to the total dwell time on both faces—averaged at the participant level for each Condition-by-Phase combination and entered into a linear mixed-effects model fitted with the lme4 package in R. Fixed effects included condition, phase, and their interaction, along with centered AQ scores and their squared terms, with gender and condition order as exploratory covariates. Participant identity was modeled as a random effect with random intercepts and by-condition slopes, and the model was fitted by restricted maximum likelihood. Fifty participants remained in the final sample after two were excluded for insufficient valid trials, and the overall valid trial rate was 99.4 percent. At baseline, dwell-time proportion sat close to chance in both conditions—0.52 in the Approach condition and 0.51 in the Recede condition—confirming that participants began with no inherent preference for either face.</p>
<p>The results hinged on a significant Condition-by-Phase interaction, β = 0.07, with a 95 percent confidence interval from 0.03 to 0.12 and p = .002. A main effect of Phase was also present, indicating overall lower dwell-time proportions at test. The pairwise comparisons told the more interesting story: in the Approach condition, dwell-time proportion significantly decreased from baseline to test, falling from a mean of 0.52 to 0.48, a change of roughly five percentage points that reached significance with a Bonferroni-corrected p value of .013. In the Recede condition, the numerical shift went the other way, rising from 0.51 to 0.54, but this increase did not reach statistical significance. Robustness checks using a logit-transformed outcome reproduced the same pattern, and model diagnostics, including DHARMa residual tests, showed no substantial deviations. Notably, none of the individual-difference or demographic covariates—AQ scores, gender, or block order—produced significant effects.</p>
<p>The direction of the approach effect deserves particular attention. A reward-learning framework might lead one to expect that a face that reliably responds to gaze with social engagement—an approach, an apparent closing of distance—would come to attract more looking, much as stimuli paired with reward continue to capture attention after the reward is gone. Instead, the participants looked less at the approaching face at test. The authors are careful about interpretation. Reduced gaze allocation, they argue, may reflect a redistribution of attention rather than subjective dislike or a stable negative evaluation of the face. One plausible account involves monitoring: during training, participants may have actively monitored the face to verify that its approach had completed, and when both faces were later presented as static, that monitoring demand was gone and attention was reallocated elsewhere. On this reading, gaze-triggered distance changes redistribute later gaze rather than simply increasing looking toward the approach-associated stimulus.</p>
<p>The authors are equally explicit about what the data cannot establish. Because the same face identities were consistently paired with specific outcomes during training and then shown as static at test, the design cannot definitively separate effects of face identity from effects of outcome history. Nor can it determine whether any association was attributed to the face itself or to the experienced gaze-triggered event. A further constraint is that approach and recede were implemented through changes in face size, so distance changes were necessarily accompanied by visual size changes; the study cannot determine whether the observed shifts reflect processing of interpersonal distance, of size, or of both. The use of neutral female faces in a screen-based task may also have limited the social salience of the signals and constrains generalizability to naturalistic interactions. The authors note that the observed effects do not imply subjective evaluation, value acquisition, or a specific learning mechanism, and that the null effect in the Recede condition could mask individual differences in the direction of gaze shifts that canceled out at the group level.</p>
<p>Even with these caveats, the paradigm opens a controlled window onto a phenomenon that most theories of social attention have treated only indirectly: the aftereffects of gaze-triggered social outcomes. In everyday life, looking at someone frequently precedes consequences—a step closer, a turn away, an approach or withdrawal—that then proceed without depending on continued gaze. The Tsukuba design isolates exactly that structure, separating the discrete triggering role of sustained gaze from the unfolding of the outcome and from any concurrent motion during assessment. The authors suggest that future work incorporating non-gaze-triggered control conditions, such as randomized onset of size changes, could establish whether the effects depend on the gaze-triggered structure itself rather than on motion per se, while varying facial expressions could test whether the modulation of gaze allocation generalizes across social and affective contexts. For now, the study delivers a provocative core finding: the eyes do not merely select the social world—they help set in motion the very outcomes that later select where the eyes will go.</p>
<p><strong>Subject of Research:</strong> How gaze-triggered changes in apparent interpersonal distance affect subsequent gaze allocation to face stimuli</p>
<p><strong>Article Title:</strong> Condition-specific changes in gaze allocation following gaze-triggered interpersonal-distance outcomes</p>
<p><strong>Article References:</strong> An, C., &amp; Matsuda, S. (2026). Condition-specific changes in gaze allocation following gaze-triggered interpersonal-distance outcomes. <em>Attention, Perception, &amp;amp; Psychophysics, 88</em>(7), Article 185. <a href="https://doi.org/10.3758/s13414-026-03322-8" rel="noopener noreferrer">https://doi.org/10.3758/s13414-026-03322-8</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.3758/s13414-026-03322-8" rel="noopener noreferrer">10.3758/s13414-026-03322-8</a></p>
<p><strong>Keywords:</strong> gaze allocation, interpersonal distance, eye tracking, social attention, gaze-triggered feedback, value-driven attention, approach and avoidance, dwell time, face perception, attentional bias, linear mixed-effects model, social cognition</p>
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