The Goldilocks effect: human infants allocate attention to visual sequences that are neither too simple nor too complex.  
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PMID: 22649492 Owner: NLM Status: MEDLINE 
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Human infants, like immature members of any species, must be highly selective in sampling information from their environment to learn efficiently. Failure to be selective would waste precious computational resources on material that is already known (too simple) or unknowable (too complex). In two experiments with 7 and 8montholds, we measure infants' visual attention to sequences of events varying in complexity, as determined by an ideal learner model. Infants' probability of looking away was greatest on stimulus items whose complexity (negative log probability) according to the model was either very low or very high. These results suggest a principle of infant attention that may have broad applicability: infants implicitly seek to maintain intermediate rates of information absorption and avoid wasting cognitive resources on overly simple or overly complex events. 
Authors:

Celeste Kidd; Steven T Piantadosi; Richard N Aslin 
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Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, NonU.S. Gov't; Research Support, U.S. Gov't, NonP.H.S. Date: 20120523 
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Title: PloS one Volume: 7 ISSN: 19326203 ISO Abbreviation: PLoS ONE Publication Date: 2012 
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Created Date: 20120531 Completed Date: 20121009 Revised Date: 20130624 
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Nlm Unique ID: 101285081 Medline TA: PLoS One Country: United States 
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Languages: eng Pagination: e36399 Citation Subset: IM 
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Brain and Cognitive Sciences, University of Rochester, Rochester, New York, United States of America. ckidd@bcs.rochester.edu 
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physiology* Child Development / physiology* Humans Infant Learning / physiology* Photic Stimulation Regression Analysis Visual Perception / physiology* 
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Journal Information Journal ID (nlmta): PLoS One Journal ID (isoabbrev): PLoS ONE Journal ID (publisherid): plos Journal ID (pmc): plosone ISSN: 19326203 Publisher: Public Library of Science, San Francisco, USA 
Article Information Download PDF Kidd et al. This is an openaccess article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Received Day: 13 Month: 12 Year: 2011 Accepted Day: 5 Month: 4 Year: 2012 collection publication date: Year: 2012 Electronic publication date: Day: 23 Month: 5 Year: 2012 Volume: 7 Issue: 5 Elocation ID: e36399 ID: 3359326 PubMed Id: 22649492 Publisher Id: PONED1124980 DOI: 10.1371/journal.pone.0036399 
The Goldilocks Effect: Human Infants Allocate Attention to Visual Sequences That Are Neither Too Simple Nor Too Complex Alternate Title:Infants Prefer Medially Complex Events  
Celeste Kidd^{1}*  
Steven T. Piantadosi^{1}  
Richard N. Aslin^{1}^{2}  
Antoni RodriguezFornellsedit1 
Role: Editor 
1Brain and Cognitive Sciences, University of Rochester, Rochester, New York, United States of America 

2Center for Visual Science, University of Rochester, Rochester, New York, United States of America 

University of Barcelona, Spain 

Correspondence: * Email: ckidd@bcs.rochester.edu Contributed by footnote: Conceived and designed the experiments: CK STP RNA. Performed the experiments: CK. Analyzed the data: CK STP. Contributed reagents/materials/analysis tools: CK STP RN. Wrote the paper: CK STP RN. 
Human infants face two daunting problems as they begin to learn about their surroundings. First, they enter the postnatal world with only rudimentary mechanisms–provided by their evolutionary heritage–for interpreting environmental information. Second, the potential information available in the environment is both voluminous and complex. These two problems led William James to coin his famous phrase about “the blooming, buzzing confusion” that confronts the newborn ^{[1]}. Nonetheless, infants show remarkable feats of learning, beginning in the last trimester of fetal life, continuing through the perinatal period, and accelerating through infancy and early childhood ^{[2]}–^{[5]}. Infants are able to extract the statistical properties of their environment in a diverse array of learning tasks and domains, including sounds, words, people, shapes, and objects ^{[6]}–^{[11]}. But how is it that infants are able to learn efficiently in such a complex environment? One solution is to have a small set of innate biases; for example, seeking to look at and listen to biologically significant stimuli such as faces and speech. However, innate biases alone cannot be the solution for the vast majority of stimuli from which infants must learn. Given the slow timecourse of evolution, we also need general purpose learning mechanisms to deal with a changing environment and with classes of stimuli that could not plausibly be processed by a small set of specialized mechanisms.
Here, we focus on this generalpurpose learning mechanism by avoiding the use of special stimuli and asking whether infants deploy a sensible (and likely implicit) strategy for allocating attention to arbitrary, neutral stimuli. Our goal is to determine whether infants are biased to gather information from the environment in a principled way that serves as a key component of an efficient learning mechanism ^{[12]}, ^{[13]}. Specifically, we provide evidence that infants avoid spending time examining stimuli that are either too simple (highly predictable) or too complex (highly unexpected) according to their implicit beliefs about the probabilistic structure of events in the world. Rather, infants allocate their greatest amount of attention to events of intermediate surprisingness–events that are likely to have just enough complexity so that they are interesting, but not so much that they cannot be understood. This approach builds on a longstanding tradition in developmental psychology, as exemplified by Piaget ^{[13]}. He argued that when children are confronted with a new piece of information, they initially attempt to incorporate it within their existing knowledge structures through a process of assimilation. When this is not possible, children either fail to learn new structures (and move on to sample other information) or they adapt by creating new knowledge structures, a process he called accommodation.
Piaget had no objective measure of assimilation or accommodation; they remained hypothetical constructs. However, in subsequent research, a proxy for these theoretical constructs centered on the relative duration of visual attention to objects or events varying in complexity or familiarity. Many researchers have speculated about what underlying mental operations are indexed by infants’ looking times or attentional patterns ^{[14]} (for review, see Aslin 2007 ^{[15]}). The generally accepted view is that looking times reflect some combination of (a) stimulusdriven attention, (b) memory of past stimuli, and (c) comparison between the current and the past stimuli. If infants are presented with an already familiar stimulus, they prefer it over a novel stimulus, but quickly tire of it after a brief period of refamiliarization (habituation), and subsequently show preferences for novel stimuli. Similarly, if repeatedly exposed to an initially novel stimulus, infant looking times decline and then recover to the presentation of another novel (i.e., completely unfamiliar) stimulus. Theoretical accounts for these familiarity and novelty preferences all share a common theme: As infants attempt to encode various features of a visual stimulus, the efficiency or depth of this encoding process determines their subsequent preferences. Familiarity preferences arise when infants have not yet completed encoding the familiar stimulus into memory, or when the novel stimulus is too dissimilar from the infants’ existing mental representations to be readily encoded ^{[16]}–^{[22]}.
However, these theories lacked an objective measure of the relevant independent variable–an event’s complexity or relationship to existing representations. Instead, researchers overwhelmingly relied on qualitative judgments of stimulus complexity to select materials to test infants’ visual preferences. These qualitative judgments relied on inferences about infants’ existing mental representations, to which researchers had no direct access. With no reasonable way of modeling infants’ existing representations, it was impossible to quantitatively measure the complexity of the information conveyed by a particular stimulus. Thus, researchers had only post hoc estimates of stimulus complexity–those obtained by measuring the very patterns of visual preferences that the theories were designed to predict. Two exceptions are Civan, Teller & Palmer 2005 ^{[23]} and Kaldy & Blaser 2006 ^{[24]} in that both papers quantified the perceptual salience of visual stimuli in order to effectively demonstrate its importance in eliciting infants’ preferences for novel versus familiar stimuli.
We overcome these problems by formalizing a notion of stimulus complexity and behaviorally testing the relationship between complexity and infants’ probability of looking away at each successive point in a sequence of events. We assume that at each point in the experiment–and in everyday life–infants have used observed data to form probabilistic expectations about what events are likely and unlikely to be observed next ^{[25]}, ^{[26]}. We model these expectations using an idealized observer model of our experimental stimuli. We then measure complexity as the negative log probability of an event according to this idealized model. This measure quantifies each event’s information content^{[27]}. (This measure has also been called surprisal^{[28]}, since it may also be interpreted as representing the “surprise” of seeing the outcome.) We show that infants preferentially look away at events that are either very simple (high probability) or very complex (low probability), according to the idealized model. Intuitively, high probability events convey little information–infants’ attentional resources are best spent elsewhere. Low probability events may indicate that the observed stimuli are unlearnable, unstructured, or difficult to use predictively in the future. Negative log probability also quantifies the number of bits of information an ideal observer would require to encode that sequence of events in memory. Thus, infants may avoid stimuli that require encoding too much information or information that could only be extracted by prolonged attention to rare events, thereby incurring a higher processing cost than shifting attention to less complex events.
The behavioral experiment measured the point, in a sequence of events, when an infant looked away from a visual display. The displayed stimuli were easily captured by a simple statistical model. In Experiment 1, we presented each infant with 42 unique animated displays, each featuring one of 42 uniquely colored and patterned boxes occluding one of 42 unique familiar objects (e.g., a ball). Each scene display began with the occluder rising and falling, thus appearing to reveal and then reobscure the object hidden behind it (Fig. 1(a) and Video S1). To maintain infants’ attention early in the experiment, the first reveal always showed an object. For example, a blue polkadotted occluder might rise to reveal a toy fire truck. On subsequent reveals, the same object appeared in the box according to some probability randomly assigned to that trial. For example, if a trial were associated with the probability of 0.3, then 30% of the time an object would be present behind the box. Probabilities ranged from 0 to 1 in increments of 0.05 (i.e., 0.0, 0.05, 0.1, 0.15, etc.), such that there were 21 possible probabilitiesofappearance that could be associated with an object on a particular trial. The sequences of object reveals thus varied in terms of their informationtheoretic properties: some events in a sequence were highly predictable (e.g., a ball appears still in the box after having appeared on each of ten previous reveals), and others were less predictable (e.g., a rattle appears to have disappeared from within the box after having appeared on each of the ten previous reveals). The objects, boxes, and order in which the probabilitiesofappearance were presented were randomized across infants, and each of the 21 probabilitiesofappearance occurred twice (for a total of 42 trials). Each animated sequence of events continued until the infant met the lookaway criterion, which was defined as gaze directed offscreen for greater than 1 consecutive second (see Video S3 for lookaway example). To address uncertainty about infants’ mental representations and their agerelated or uniquely individual processing speeds and biases for stimulus salience, we exhaustively randomized and counterbalanced all of these extraneous variables (e.g., sequence order, object identity, object familiarity, spatial location).
We modeled the sequences of reveals using a Markov Dirichletmultinomial model (MDM). The Dirichletmultinomial is a generalpurpose statistical model that uses observed event counts to compute a posterior distribution for an underlying multinomial distribution on events. The Dirichletmultinomial makes parametric assumptions about the form of the prior probability and the likelihood of an event and is often used in Bayesian statistics because of its computational simplicity (see Materials and Methods). We apply this to a timeseries of events by making a Markov assumption that each event is statistically independent (i.e., not dependent on the ordering of the preceding events). Thus, the model can take some previously observed sequence of events–corresponding to an individual infant’s observations before they have looked away–and compute the probability of every possible next event. We hypothesize that infants’ probability of looking away at the next event in a sequence is at least partially determined by the informationtheoretic properties of that event, according to the model. Specifically, at each point in a sequence of events, the model assigns each event a probability, and the negative log of this probability provides a natural informationtheoretic measure of the complexity of the next event according to the model’s current expectations about which events are likely.
Fig. 2 illustrates the logic of the experiment and analysis. In the first example, the observer sees a sequence of four A events in a row. In this case, the observed data consist of entirely A’s. These data are combined with the prior–essentially a smoothing term to avoid zero probabilities–to form an updated posterior belief with high probability of A but nonzero probability of B (“Updated belief” column). The complexity (negative log probability) of the next event is determined using this posterior, which represents the model’s updated belief about the true distribution of events. Thus, if the next event is an A–an event that is highly likely according to the model’s posterior–the complexity of that event would be low (i.e., the event would be highly predictable according to the model). We hypothesize that infants would be more likely to look away at this event. Conversely, if the previous observations assign A very low probability (second example), A will have very high complexity (i.e., the event would be highly surprising according to the model) and infants should terminate the sequence of events by looking away. If the previous observations make A moderately likely (third example), the occurrence of an A event will convey a “Goldilocks” amount of information, leading infants to be less likely to look away. If infants do not look away, then the modeling step is repeated for the next item in the sequence. This means that infants may look away at different points in different sequences, but we predict systematicity in these lookaways: regardless of how far into a sequence an infant has made it without looking away, their probability of looking away on the next object will depend on its complexity, conditioning on all previous observations.
We note that this type of modeling and analysis contrasts with most previous infant studies, which typically tested for differences in overall mean looking times. Here, we are predicting a binary outcome (whether an infant looks away) at each individual event in the sequence. This is a more precise prediction based on probabilities computed online.
Fig. 3 shows infants’ probability of looking away, as a function of that event’s negative log probability according to the model, and collapsing across infants, sequences, and sequence positions. The diamonds show raw probability of lookaway, binning complexity into 5 discrete bins. The curve represents the fit of a Generalized Additive Model ^{[29]}, which attempts to find a smooth relationship between complexity and lookaway probability. This figure shows a Ushaped relationship between infant lookaway probability and the online modelbased estimate of complexity, with infants looking away from events that are especially predictable or especially surprising. There is a “Goldilocks” value of complexity around 1.25 bits, corresponding to infants’ preferred information rate in this task.
Although the plot in Fig. 3 provides a revealing picture of the relationship between indexes of complexity and looking durations, there are likely other factors that influence when infants will look away from the displays. For instance, lowinformation and highinformation events may tend to occur later in a sequence, after learners have developed expectations about the distributional properties of the events. If infants tend not to look away early, perhaps because they are initially captured by the salience of the display independent of its complexity, they would appear to disprefer low and high complexity. To address this potential confound, we performed a regression analysis that controls for the influence of temporal and other factors on lookaway probability. When infants look away in a trial, they provide no more data for the remainder of the trial. Because of this, such data violate the independence assumptions of standard logistic (or linear) regression. An appropriate model for this kind of data–used primarily in biostatistics to study, for example, predictors of mortality–is known as a survival analysis^{[30]}, ^{[31]}. We used a type of survival analysis known as a Cox regression, that measures the log linear influence of predictors on lookaway probability, while respecting the fact that once infants look away they provide no additional data on the same trial. Importantly, this regression also controls for a baseline lookaway distribution, which is fit nonparametrically to the data, thereby removing the influence of an average distribution of looking times before testing the significance of the other predictors. We note that this regression does not include subject effects, but we develop more sophisticated analysis methods that include a range of subject effects in forthcoming work ^{[32]}.
We included a number of control covariates that could plausibly influence infant lookaways using a stepwise procedure that only added variables that improved model fit. These variables included whether an object was present, whether the presence of the object was the same as the previous reveal, how many sequences the infant had already observed, and the uncertainty in the model about the correct distribution of events. This was measured by the differential entropy of the multinomial parameters in the MDM model. We also included linear and quadratic complexity terms. To aid in interpretation of the regression coefficients, complexity was standardized before being squared (i.e., it was shifted and scaled to have mean 0 and standard deviation 1) to test for a significant quadratic trend of complexity on lookaways. This stepwise procedure revealed a significant effect only for squared complexity ( ), and no other variables (see Table 1). This indicates that the Ushape observed in Fig. 2 is statistically significant, even after controlling for an overall baseline lookaway distribution and the other potentially confounding variables (see Materials and Methods). The magnitude of this effect can be understood by considering , which is the factor that the baseline lookaway probability is multiplied by for each increase in squared surprisal of standard deviation from the overall mean in the experiment. This effect is relatively small, though statistically reliable.
In Experiment 1, objects were either present or absent from behind a single occluder. Perhaps a more typical context in real life, though, is for different events to occur in a multiobject scene, thereby allowing infants’ attention to be attracted to both individual events and transitions between events. In Experiment 2, we presented each infant with 32 unique sequentialevent displays (Fig. 1(b) and Video S2). Each display presented an animated scene consisting of three uniquely patterned boxes, each concealing a unique familiar object (e.g., a cookie). The locations of the three boxes for a given sequence were chosen randomly but remained static throughout a scene. The box locations were randomly shuffled between event sequences, but no more than two boxes appeared on either half of the screen. Neither the patterns on the boxes nor the objects were repeated across event sequences so that each objectbox pair was independent and unique. Each event in a sequence consisted of an object that popped out of a box, and then back into the box. Each event lasted 2 seconds in total duration (1second “popup”, 1second “popdown”). Events were presented sequentially with no overlap or delay. The same 32 event sequences were presented to every infant. However, the objects, boxes, and order in which the 32 event sequences were presented were randomized across infants. This design ensured that differences in looking times across event sequences were not driven by differences in scene items or presentation order. Each animated sequence of events continued until the infant met the lookaway criterion, which was defined as gaze directed offscreen for greater than 1 consecutive second.
Results from Experiment 2 are shown in Fig. 4. As in Experiment 1, there is a Ushaped relationship between lookaway probability and complexity, as measured by the same MDM model (assuming event independence) used in Experiment 1. The Cox regression for Experiment 2 included all of the covariates used in Experiment 1, except whether an object was present, since there was always an object popping up from behind one of the three boxes. However, because there are three different boxobject pairs in each scene, we also included covariates measuring whether the current event is the first time an object has appeared from behind a box, and a factor measuring how many objects have not yet popped up. Results of this analysis are shown in Table 1. As in Experiment 1, this analysis revealed significant effects of squared complexity ( ). Here, , meaning that each increase of squared complexity standard deviation from the mean resulted in a lookaway probability that was a factor of times greater. This is a much larger effect than that found in Experiment 1. There was also a significant linear effect of complexity, indicating that the U is not symmetric about the mean ( ), and an effect of trial number, likely representing effects of fatigue ( ), although this is small compared to the complexity effects ( ).
We also applied the MDM model to the data from Experiment 2 under an assumption of eventorder dependence. That is, instead of treating every event as independent, we examined whether lookaways were predicted by the immediately preceding event (i.e., a transitional model). Fig. 5 shows that a Ushaped function also describes this transitional model, and the Cox regression confirms that this effect is highly significant ( ). This analysis also revealed an effect of trialnumber ( ).
Finally, one can ask which of the two models better accounts for infants’ behavior on the task in Experiment 2. The predictions of the transitional and nontransitional models are difficult to distinguish because they are closely related: Complexity of both models is correlated at ( ). However, if both are entered into a Cox regression along with all variables found to be significant, the transitional complexity is significant ( ), but the nontransitional complexity is not ( ). This provides strong evidence that infants track transitional probabilities, but the null result for the nontransitional model is difficult to interpret due to its correlation with the transitional model and the noise inherent in infant data.
The results of the experiments reported here have important implications for two interrelated hypotheses concerning infants’ attention. First, infants behave as if they are employing a principled inferential process for learning about events in the world. The particular MDM model used in our analyses took as inputs a series of observed events or transitions between events to form probabilistic expectations about what events are most likely to occur in the future. The model was necessary to determine what complexity a set of stimulus events conveys to an ideal observer. A failure of either of these components–the probabilistic model or the linking assumption that maps level of complexity onto looking times–would have yielded null results.
Second, infants appear to allocate their attention in order to maintain an intermediate level of complexity. A powerful feature of our analyses was the ability, via the Cox regression, to control for potential confounds such as the number of items that have not appeared yet, item repeats, and an arbitrary baseline distribution of lookaway probabilities. To our knowledge, the hypothesis that infants prefer a particular level of information has not been tested while controlling for these other variables, and our analyses therefore provide several methodological advances. Rather than predicting infants’ average looking time to a stimulus, our analyses predicted the precise event in a sequence when an infant would terminate (i.e., look away from) the display. Although others have observed Ushaped behavior in infants under some circumstances, our results provide the first evidence that the informationtheoretic properties of a formal model provide a significant predictor of infant lookaways, over and above the effects of other variables, for a large set of arbitrary, neutral visual stimuli. Interestingly, this Ushaped pattern is similar to those obtained with many earlier models of visual attention based on depth of processing or difficulty of encoding the stimulus ^{[17]}–^{[19]}. This could indicate that while earlier models did not computationally define the stimulus properties they hypothesized as the mediators of infant looking times (i.e., complexity), the properties they explored are nevertheless relevant in guiding infants’ visual attention. Our results also provide a formal account for why infants show novelty preferences (when two test stimuli fall on the left half of the Ushaped function, the stimulus with greater complexity elicits more attention) or familiarity preferences (when two test stimuli fall on the right half of the Ushaped function, the stimulus with lesser complexity elicits more attention).
Similar hypotheses about how adults allocate their limited resources in the language domain–for example, those supporting a uniform information principle ^{[33]}–^{[37]}–may suggest that what we have observed in infants reflects a ubiquitous constraint across domains and developmental levels. In addition, other theories propose that learners allocate attention to stimuli containing just the right level of complexity because optimal complexity triggers just the right amount of “arousal” in the learner ^{[38]}. The Ushaped function may result from the basic response properties of neural systems ^{[39]}, although determining the precise mechanism will require further research.
In summary, our findings are consistent with theories that suggest infants actively seek to maintain an intermediate level of information absorption, avoiding allocating cognitive resources to either overly predictable or overly surprising events. It is important to note that we are not claiming that this Goldilocks effect is the only factor in infants’ allocation of attention. Certainly, there are speciestypical preferences and effects of learning that can dominate infants’ attentional behavior. We argue that when these other factors are controlled for, there remains a significant Ushaped effect of complexity that is well accounted for by our model. Further investigation is required to determine how infants’ preference for intermediate levels of information affects the outcome of learning, either by enhancing the rate of learning or its asymptotic level.
All research was approved by the Research Subjects Review Board at the University of Rochester (protocol RSRB00024570). Parents volunteering their infants for the study were fully informed of the study procedures and completed written informed consent and permission forms in advance of the study.
In Experiments 1 and 2, we presented infants with animated displays depicting event sequences varying in their predictability. All displays featured uniquely colored and patterned boxes (e.g., pink polka dots) that were animated to reveal unique familiar objects (e.g., a ball; see Videos S1 and S2 for examples). A Matlab script was used to generate each of the animated displays. Neither the boxes nor the objects were repeated across event sequences so that each objectbox pair was independent and unique. The objects, boxes, and order in which the event sequences were presented were also randomized across infants. This design ensured that differences in looking time across event sequences were not driven by differences in scene items or presentation order.
In Experiment 1, each animated sequence featured one unique object occluded by one box. The box opened (1 second) and closed (1 second) repeatedly, each time revealing the contents of the box. The object always appeared in the box on the first reveal event. On subsequent reveal events, the object was either present or absent depending on the predictability of the event sequence selected for that trial (a value between 0 and 1). So, for example, a single trial might feature a purple striped box occluding a small toy train with a probabilityofappearance of 0.5. The sequence of events (object appears = 1, empty box = 0) might be: 1, 1, 0, 1, 0, 1, 0, 1, 0, 0. The reveals were presented sequentially with no overlap or delay. There were 21 unique probabilitiesofappearance (increments of 0.05 between 0 and 1, e.g., 0, 0.05, 0.1, 0.15, …) and all were presented to each infant twice (42 trials in total) in a random order.
In Experiment 2, each animated display featured three boxes of three unique colors and patterns (e.g., yellow stripes, blue polka dots, green stars), each concealing a unique object (e.g., a cookie, a spoon, a car). The locations of the three boxes for a given sequence were chosen randomly but remained static throughout a scene. The box locations were randomly shuffled on the screen between event sequences, with the constraint that no more than two boxes appeared on either half of the screen. Each event in a sequence consisted of one of the three unique objects popping out from behind one of the three boxes (1 second), and then back into the box (1 second). Thus, the total duration of each event was 2 seconds, and events were presented sequentially with no overlap or delay. There were 32 unique event sequences that varied in the probability that each of the three objects appeared from behind their respective occluding boxes. Some sequences were simple (e.g., A, A, A, A, A, A, …), while others were more complex (e.g., A, B, A, B, A, C, …). All event sequences were presented to each infant (32 trials in total).
The procedures for Experiments 1 and 2 were identical, with two exceptions: the type of displays used (singlebox in Experiment 1 and threebox in Experiment 2) and the number of trials presented to each infant (42 in Experiment 1 and 32 in Experiment 2). Each infant was seated on his or her parent’s lap in front of a tablemounted Tobii 1750 eyetracker. The infant was positioned such that his or her eyes were approximately 23 inches from the monitor, the recommended distance for accurate eyetracking. At this viewing distance, the 17inch LCD screen subtended 24×32 degrees of visual angle. Each of the three boxes was 5×5 degrees. To prevent parental influence on the infant’s behavior, the parent holding the infant was asked to wear headphones playing music, wear a visor, lower their eyes, and abstain from interacting with their infant throughout the experiment.
Each trial was preceded by an animation designed to attract the infant’s attention to the center of the screen–a laughing and cooing baby. Once the infant looked at the attentiongetter, an experimenter who was observing remotely pushed a button to start the trial. For each trial, an animated scene–featuring a single box in Experiment 1, or three boxes in Experiment 2–was played. The animated sequences of reveal events continued until the infant looked away continuously for 1 second, or until the sequence timed out at 60 seconds. The 1second lookaway criterion for trial termination was automatically determined by the Tobii eyetracking software. If the infant looked continuously for the entire 60second sequence, the trial was automatically labeled as a “time out” and discarded before the analysis (2.4% of trials in Experiment 1, 5.4% of trials in Experiment 2). If the trial was terminated before the infant actually looked away, the trial was labeled by an experimenter as a “false stop” and also discarded. False stops, as determined by a separate video recording of the infant’s face, occurred as a result of the Tobii software being unable to detect the infant’s eyes continuously for 1 second, usually due to the infant inadvertently blocking the eyetracker camera’s view of his or her own eyes with head or arm movements (22.1% of trials in Experiment 1, and 20.7% of trials in Experiment 2). Trials in which the infant looked for fewer than four events were also discarded, since it is presumed that too few observations are insufficient for establishing expectations about the distribution of events.
In Experiment 1, 42 infants (mean = 7.9 months, range = 7.0  8.9) were included in the analysis. Fortyfour infants were tested; one infant was excluded due to excessive tiredness (he fell asleep within the first few trials and could not be awakened), and one was excluded due to fussiness. In Experiment 2, 30 infants (mean = 7.6 months, range = 7.0  8.8) were tested, and all participating infants completed the study. In both studies, all infants were born fullterm and had no known health conditions, hearing loss, or visual deficits according to parental report.
Intuitively, infants observe how many times each event occurs in the world, and then use these event counts to infer an underlying probability model of their observations. In Experiment 1, the two possible events are that the screen lifts to reveal that an object is either present or absent. In Experiment 2, there are three possible events corresponding to which of three objects appears from behind its box.
An observer who sees only a single event happen would not likely infer that the single observed event is the only one possible (i.e, has probability of 1); instead, observers likely bring expectations to this learning task. In the MDM model used here, this prior expectation is parameterized by a single free parameter, , which controls the strength of the learner’s prior belief that the distribution of events is uniform. As gets large, the model has strong prior beliefs that the distribution of events in the world is uniform; as approaches zero, the model believes more strongly that the true distribution closely resembles that of the empirically observed event counts. In modeling, we chose a value of = 1, corresponding to a uniform prior expectation about the distribution of events (with expected values 5050 in Experiment 1 and 333333 in Experiment 2). However, the qualitative results–in particular, the Ushaped relationship between complexity and lookaway probability–do not depend strongly on the choice of .
Formally, suppose there are events, , and the th event has been observed times. We are interested in estimating (or scoring) a multinomial distribution parameterized by where is the true (unobserved) probability of event . Under a DirichletMultinomial model,
where is a normalizing constant that depends on the and That is, after observing each event type occur some number of times, the infant may form a representation, of their guess at the true distribution of events. Every distribution can be scored according to Equation 1, allowing one to compute how strongly a learner should believe that any particular is the correct one. We predict that infants’ likelihood of looking away at a current event will depend upon the complexity of that current event, which is determined by both the previously observed events and the identity of the current event. We predict that events of either very low complexity (highly predictable) or very high complexity (highly surprising) will be more likely to trigger a lookaway than events with moderate complexity.When the th event occurs, the main variable of interest here is its negative log probability according to the model. We compute this by integrating over the above posterior distribution on . This corresponds to a measure of the information conveyed by observing event according to an ideal Bayesian learner who had seen all previous events. We predicted that infants would be more likely to look away during events that contained either too little or too much information, giving a Ushaped (quadratic) relationship between this negative log probability measure and the actual observed lookaway probability.
An example of an animated singlebox display used in Experiment 1.
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Click here for additional data file (pone.0036399.s001.mov)
Video S2
An example of an animated threebox display used in Experiment 2.
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Click here for additional data file (pone.0036399.s002.mov)
Video S3
A 7monthold subject attending to a threebox display in Experiment 2, and then looking away (and subsequently terminating the trial).
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Click here for additional data file (pone.0036399.s003.mov)
Notes
Competing Interests: The authors have declared that no competing interests exist.
Funding: CK and STP were supported by Graduate Research Fellowships from the National Science Foundation (www.nsf.gov). The research was supported by grants from the National Institutes of Health (HD37082, www.nih.gov) and the J. S. McDonnell Foundation (220020096, www.jsmf.org) to RNA. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
We thank Johnny Wen for his help with Matlab programming; Holly Palmeri, Laura Zimmermann, and Alyssa Thatcher for their help preparing stimuli and collecting infant data; Allyssa Abel, Madeleine Chansky, Suzanne Horwitz, Katheryn Lukens, Maddie Pelz, Hillary Snyder, Laura Socwell, Lindsay Woods, and Rosemary Ziemnik for their help recruiting and scheduling subjects; and Michael Tanenhaus, Elissa Newport, Josh Tenenbaum, Daphne Bavelier, Ed Vul, Matthew G. McGovern, Katherine S. White, Dan Yurovsky, Roger Levy, Scott Johnson, two anonymous reviewers, and members of CoCoSci, TedLab, and the Aslin and Newport labs for their helpful comments and suggestions.
References
1.  James W. Year: 1890The Principles of Psychology.Cambridge, MAHarvard University Press 
2.  DeCasper AJ,Fifer WP. Year: 1980Of human bonding: Newborns prefer their mothers’ voices.Science208117411767375928 
3.  RoveeCollier CK,Sullivan MW,Enright M,Lucas D,Fagan JW. Year: 1980Reactivism of infant memory.Science2081159617375924 
4.  Siqueland ER,De Lucia CA. Year: 1969Visual reinforcement of nonnutritive sucking in human infants.Science165114411465801599 
5.  Stevenson HW. Year: 1972Children’s Learning.New YorkAppletonCenturyCrofts 
6.  Fiser J,Aslin RN. Year: 2002Statistical learning of new visual feature combinations by infants.Proceedings of the National Academy of Sciences of the United States of America991582212429858 
7.  Kirkham NZ,Slemmer JA,Johnson SP. Year: 2002Visual statistical learning in infancy: Evidence for a domain general learning mechanism.Cognition83B35B4211869728 
8.  Maye J,Werker JF,Gerken LA. Year: 2002Infant sensitivity to distributional information can affect phonetic discrimination.Cognition82B101B11111747867 
9.  Saffran JR,Aslin RN,Newport EL. Year: 1996Statistical learning by 8monthold infants.Science27419268943209 
10.  Saffran JR,Johnson EK,Aslin RN,Newport EL. Year: 1999Statistical learning of tone sequences by human infants and adults.Cognition70275210193055 
11.  Saylor MM,Baldwin DA,Baird JA,LaBounty J. Year: 2007Infants’ online segmentation of dynamic human action.Journal of Cognition and Development8113128 
12.  Berlyne DE. Year: 1960Conflict, Arousal, and Curiosity, volume 331.New YorkMcGrawHill 
13.  Piaget J. Year: 1970Structuralism.New YorkHarper & Row 
14.  Fantz RL. Year: 1964Visual experience in infants: Decreased attention to familiar patterns relative to novel ones.Science14666814191712 
15.  Aslin RN. Year: 2007What’s in a look?Developmental Science10485317181699 
16.  Dember WN,Earl RW. Year: 1957Analysis of exploratory, manipulatory, and curiosity behaviors.Psychological Review64919613420283 
17.  Hunter MA,Ames EW. Year: 1988A multifactor model of infant preferences for novel and familiar stimuli.Advances in Infancy Research56995 
18.  Kinney DK,Kagan J. Year: 1976Infant attention to auditory discrepancy.Child Development47155164954493 
19.  Roder BJ,Bushnell EW,Sasseville AM. Year: 2000Infants’ preferences for familiarity and novelty during the course of visual processing.Infancy1491507 
20.  Rose SA,Gottfried AW,MelloyCarminar P,Bridger WH. Year: 1982Familiarity and novelty preferences in infant recognition memory: Implications for information processing.Developmental Psychology18704713 
21.  Sokolov E. Year: 1963Perception and the Conditioned Reflex.Oxford, EnglandPergamon 
22.  Wagner SH,Sakovits LJ. Year: 1986A process analysis of infant visual and crossmodal recognition memory: Implications for an amodal code.Advances in Infancy Research4195217 
23.  Civan A,Teller DY,Palmer J. Year: 2005Relations among spontaneous preferences, familiarized preferences, and novelty effects: Measurements with forcedchoice techniques.Infancy7111142 
24.  Kaldy Z,Blaser EA,Leslie AM. Year: 2006A new method for calibrating perceptual salience across dimensions in infants: the case of color vs. luminance.Developmental Science948248916911450 
25.  Téglás E,Vul E,Girotto V,Gonzalez M,Tenenbaum JB,et al. Year: 2011Pure Reasoning in 12 MonthOld Infants as Probabilistic Inference.Science332105421617069 
26.  Xu F,Garcia V. Year: 2008Intuitive statistics by 8monthold infants.Proceedings of the National Academy of Sciences of the United States of America1055012501518378901 
27.  Shannon CE. Year: 1948A Mathematical Theory of Communication.Bell System Technical Journal27379423 
28.  Tribus M. Year: 1961Thermostatics and thermodynamics: an introduction to energy, information and states of matter, with engineering applications.New YorkD. Van Nostrand 
29.  Hastie T,Tibshirani R. Year: 1990Generalized Additive Models.Boca RatonChapman and Hall/CRC 
30.  Hosmer DW,Lemeshow S,May S. Year: 2008Applied Survival Analysis: Regression Modeling of TimetoEvent Data, Second Edition.Hoboken, NJJohn Wiley and Sons 
31.  Klein J,Moeschberger M. Year: 2003Survival Analysis: Techniques for Censored and Truncated Data, Second Edition.New YorkSpringerVerlag 
32.  Piantadosi ST,Kidd C,Aslin RN. Year: forthcoming) RRich methods for infant looking times 
33.  Aylett M,Turk A. Year: 2004The smooth signal redundancy hypothesis: A functional explanation for relationships between redundancy, prosodic prominence, and duration in spontaneous speech.Language and Speech473115298329 
34.  Genzel D,Charniak E. Year: 2002Entropy rate constancy in text.Proceedings of the 40th Annual Meeting of the Association for Computational LinguisticsStroudsburg, PAAssociation for Computational Linguistics199206 
35.  Piantadosi ST,Tily H,Gibson E. Year: 2011Word lengths are optimized for efficient communication.Proceedings of the National Academy of Sciences of the United States of America10893526352921278332 
36.  Jaeger TF. Year: 2010Redundancy and reduction: Speakers manage syntactic information density.Cognitive Psychology61236220434141 
37.  Levy R,Jaeger TF. Year: 2007Speakers optimize information density through syntactic reduction.Advances in Neural Information Processing Systems19849 
38.  Yerkes RM,Dodson JD. Year: 1908The relation of strength of stimulus to rapidity of habitformation.Journal of Comparative Neurology and Psychology18459482 
39.  TurkBrowne NB,Scholl BJ,Chun MM. Year: 2008Habituation in infant cognition and functional neuroimaging.Frontiers in Human Neuroscience211118958202 
40.  Akaike H. Year: 1974A new look at the statistical model identification.IEEE Transactions on Automatic Control196716723 
Figures
[Figure ID: pone0036399g001] 
doi: 10.1371/journal.pone.0036399.g001. Figure 1 Examples of visual displays used in Experiments 1 and 2. a) The object (e.g., a toy fire truck) in the box for Experiment 1 was revealed (or not) by updown animation of an occluder (e.g., a blue polkadotted box). b) In Experiment 2, one of three unique objects (e.g., a baby bottle) popped up from behind one of three highly distinctive boxes. Also see Videos S1 and S2 for examples of animated displays used in these studies. 
[Figure ID: pone0036399g002] 
doi: 10.1371/journal.pone.0036399.g002. Figure 2 Schematic showing several example event sequences and how the ideal observer model combines observed events with a simple prior to form expectations about upcoming events. The next event then conveys some amount of information according to these probabilistic expectations, which is related to infants’ probability of lookaway at a specific next event by a Ushaped function. 
[Figure ID: pone0036399g003] 
doi: 10.1371/journal.pone.0036399.g003. Figure 3 Ushaped curve for singlebox display used in Experiment 1. The solid curve represents the fit of a Generalized Additive Model (GAM) ^{[29]} with binomial link function, relating complexity according to the MDM model ( axis) to infants’ lookaway probability ( axis). The dashed curves show standard errors according to the GAM. The GAM fits include the effect of complexity (negative log probability) and the effect of position in the sequence. Note, the error bars and GAM errors do not take into account subject effects. Vertical spikes on the axis represent data points collected at each complexity value. The red diamonds represent the raw lookaway probabilities binned along the axis. 
[Figure ID: pone0036399g004] 
doi: 10.1371/journal.pone.0036399.g004. Figure 4 Ushaped curve for threebox display used in Experiment 2. The solid curve represents the fit of a GAM, relating complexity as measured by the nontransitional MDM (assuming event independence) to lookaway probability. Dashed curves show GAM standard errors. The GAM fits include the effect of complexity (negative log probability) and the effect of position in the sequence. Note, the error bars and GAM errors do not take into account subject effects. Vertical spikes on the axis represent data points collected at each complexity value. The red diamonds represent the raw lookaway probabilities binned along the axis. 
[Figure ID: pone0036399g005] 
doi: 10.1371/journal.pone.0036399.g005. Figure 5 Ushaped curve for threebox display used in Experiment 2. The solid curve represents the fit of a GAM, relating complexity as measured by the transitional MDM to lookaway probability. Dashed curves show GAM standard errors. The GAM fits include the effect of complexity (negative log probability) and the effect of position in the sequence. Note, the error bars and GAM errors do not take into account subject effects. Vertical spikes on the axis represent data points collected at each complexity value. The red diamonds represent the raw lookaway probabilities binned along the axis. 
Tables
Table 1 Cox Regression Coefficients.
Covariate  Coefficient  exp(coefficient)  Standard error  Zstatistic  Pvalue 
Experiment 1  
Squared complexity  0.052  1.05  0.026  1.969  0.049 
Experiment 2  Nontransitional model  
Complexity  −0.216  0.805  0.094  −2.29  0.022 
Squared complexity  0.269  1.308  0.109  2.47  0.013 
Trial number  0.029  1.030  0.007  3.99  6.5.10^{–5} 
Model uncertainty  0.261  1.298  0.174  1.50  0.13 
Experiment 2  Transitional model  
Squared complexity  0.356  1.43  0.084  4.27  1.9.10^{–5} 
Trial number  0.027  1.03  0.007  3.65  2.7.10^{–4} 
First appearance  0.500  1.64  0.272  1.82  0.069 
All variables found in Experiments 1 and 2 that were added by the stepwise procedure. Note that some nonsignificant variables are added because the stepwise comparison is based on the Akaike information criterion ^{[40]}. These results reveal significant quadratic effects of complexity in both experiments. Complexity and squared complexity were shifted and scaled to have mean of and standard deviation of before being entered into the regression.
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