Differential reinforcement of other-than-vocalization as a control procedure in the conditioning of infant vocalization rate

The purpose of the present study is to demonstrate reinforcement control over infant vocalization rates using a DRO schedule to control for elicitation of social stimulation. Mothers of four 2 1/2- to 3-month-old infants provided social reinforcement for their infants' vocalization under two schedules: continuous reinforcement (CRF) and differential reinforcement of other-than-vocalization (DRO). In a repeated-reversal single-subject experimental design, all four infants produced systematically higher vocalization rates during CRF, even though densities of social stimulation during DRO were equal to or greater than densities provided during CRF. Thus, whatever its elicitation value, social stimulation may reinforce infant vocalization rates.     

A parametric variation of delayed reinforcement in infants.

This study is an exploration of the parameters of delayed reinforcement with 6 infants (2 to 6 months old) in two experiments using single-subject repeated-reversal designs. In Experiment 1, unsignaled 3-s delayed reinforcement was used to increase infant vocalization rate when compared to a differential-reinforcement-of-other-than-vocalization condition and a yoked, no-contingency comparison condition. In Experiment 2, unsignaled 5-s delayed reinforcement was used to increase infant vocalization rate when compared to an alternating-treatments comparison condition. The alternating-treatments comparison consisted of 3-min components of differential reinforcement of other behavior and 3-min components of a nontreatment baseline. Successful conditioning was obtained in both experiments. These results contrast with those of previous infancy researchers who did not obtained conditioning with delays of 3 s and who attributed their findings to the limitations of the infant's memory capacity. We present an alternative conceptual framework and methodology for the analysis of delayed reinforcement in infants.     

Reinforcement of vocalizations through contingent vocal imitation

Maternal vocal imitation of infant vocalizations is highly prevalent during face-to-face interactions of infants and their caregivers. Although maternal vocal imitation has been associated with later verbal development, its potentially reinforcing effect on infant vocalizations has not been explored experimentally. This study examined the reinforcing effect of maternal vocal imitation of infant vocalizations using a reversal probe BAB design. Eleven 3- to 8-month-old infants at high risk for developmental delays experienced contingent maternal vocal imitation during reinforcement conditions. Differential reinforcement of other behavior served as the control condition. The behavior of 10 infants showed evidence of a reinforcement effect. Results indicated that vocal imitations can serve to reinforce early infant vocalizations.     

Acquisition of a spatially defined operant with delayed reinforcement.

Two experiments investigated the role of an immediate, response-produced auditory stimulus during acquisition, via delayed reinforcement, of a response selected to control for possible unprogrammed, operandum-related sources of response feedback. Experimentally naive rats were exposed to a delayed-food reinforcement condition, specifically a tandem fixed-ratio 1 differential-reinforcement-of-other-behavior 30-s schedule. The response was defined as breaking a photocell beam located near the ceiling at the rear of the operant conditioning chamber. In Experiment 1, rates of photobeam breaking by each rat increased from near zero, regardless of the presence or absence of a tone that immediately followed the response initiating the delay interval. Though not essential, the tone facilitated response acquisition and resulted in more efficient response patterns at stability. Experiment 2 demonstrated that photobeam-breaking response rates under the delayed reinforcement contingency exceeded those in a preceding baseline condition in which no food was delivered. In addition, upon introduction of the delayed reinforcement procedure, correspondence between response patterns and the requirements of the reinforcement schedule increased over baseline levels in the absence of a food contingency. Together with a previous report of Lattal and Gleeson (1990), the present results suggest that response acquisition with delayed reinforcement is a robust phenomenon that may not depend on a mechanically defined response or an immediate external stimulus change to mediate the temporal gap between response and reinforcer.     

Effect of signaled reinforcement on response variability

Three experiments examined the effect of signaling reinforcement on rats' lever pressing on contingencies that reinforced variable responding to extend the exploration of signaled reinforcement to a schedule that has previously not been examined in this respect. In Experiment 1, rats responding on a lag-8 variability schedule with signaled reinforcement displayed greater levels of variability (U values) than rats on the same schedule lacking a reinforcement signal. In Experiment 2, rats responding on a differential reinforcement of least frequent responses schedule also displayed greater operant variability with a signal for reinforcement compared with rats without a reinforcement signal. In Experiment 3, a reinforcement signal decreased the variability of a response sequence when there was no variability requirement. These results offer empirical corroboration that operant variability responds to manipulations in the same manner as do other forms of operant response and that a reinforcement signal facilitates the emission of the required operant.     

Vocalization and looking behaviour of Down's syndrome infants.

The effect of contingent and non-contingent vocal stimulation on vocalization and looking behaviour was investigated for 10 Down's syndrome infants. There were two experimental sessions consisting of four stages, namely 1 min base-line, 1 min experimental condition, a further 1 min base-line and a final 2 min experimental condition. Maternal vocal stimulation was contingent upon infant vocalization for the experimental conditions of one session and was presented every 10 s independent of infant vocalization for the experimental conditions of the other session. Neither condition increased infant vocalization but there was a significant decrease in looking at mother during the base-line stages which followed maternal vocalization (F = 5.07, d.f. = 4, 28, P less than 0.01). It is suggested that looking behaviour may be an important indication of competence in pre-linguistic social communication for developmentally delayed infants.     

Noncontingent reinforcement without extinction plus differential reinforcement of alternative behavior during treatment of problem behavior

The effects of noncontingent reinforcement (NCR) without extinction during treatment of problem behavior maintained by social positive reinforcement were evaluated for five individuals diagnosed with autism spectrum disorder. A continuous NCR schedule was gradually thinned to a fixed‐time 5‐min schedule. If problem behavior increased during NCR schedule thinning, a continuous NCR schedule was reinstated and NCR schedule thinning was repeated with differential reinforcement of alternative behavior (DRA) included. Results showed an immediate decrease in all participants’ problem behavior during continuous NCR, and problem behavior maintained at low levels during NCR schedule thinning for three participants. Problem behavior increased and maintained at higher rates during NCR schedule thinning for two other participants; however, the addition of DRA to the intervention resulted in decreased problem behavior and increased mands.     

Eye contact as a setting event for infant learning

Three-month-old human infants received social reinforcement contigent upon each vocalization. The experimenter wore eye glasses with lenses composed of clear acetate, skin-toned opaque shields, or life-size photographs of the experimenter's eyes (with direct or averted gaze), and maintained visual contact with the infant's eyes (via pinholes in the lenses) during all sessions. Each group of three subjects experienced two of the four possible lens conditions. During baseline and extinction sessions vocalization rate was quite similar under each lens condition. During conditioning sessions, however, vocalizations exceeded baseline rates in all but the opaque lens condition. In this study eye contact was neither a reinforcing, discriminative, nor eliciting stimulus. Eye contact was a setting stimulus (catalyst) for the response-reinforcement relationship.     

Influence of a televised model's vocalization pattern on infants

To assess the influence of a televised model's vocalizations on the vocal patterns of infant viewers, 32 infants at 6 months of age were presented either a televised adult model repeating a novel phoneme pattern (/ba/ba/ba/ba) or a control televised presentation of adult conversation selected from typical daytime programming. Sequential analyses of infant vocalizations revealed that infants exposed to the televised model altered their vocalization pattern, as indicated by a significant increase over base line levels in their production of a patterned series of discrete vocalizations. Infants exposed to the televised conversation showned no increase in this pattern of vocalization, and none of the infants in the study produced the novel phoneme (/ba/). The results indicate that televised presentation of discrete, repeated vocalizations can have an influence on the vocalization pattern of infants. The potential role of television in infant development is discussed.     

Patterning of infant vocal behavior

Three-month-old infants received two consecutive 5-minute periods of adult social stimulation. In both periods the adult talked, smiled, and touched the infant and in a natural manner tried to elicit vocalizations from the infant. In the first period the adult became unresponsive for 5 sec contingent upon each infant vocalization (time-out, negative reinforcement). In the second period the infant received the same number of time-out periods at the same intervals but independently of vocal responding (yoked, noncontingent control). Negative reinforcement did not suppress infant vocal rate, but the contingent withdrawal of social stimulation did cause the infant to pause more frequently between vocal responses. These pauses generally occurred immediately after the contingently, as compared with the noncontingently, delivered time-out period. The infant appears to recognize the difference between contingent and noncontingent stimulation and pauses after the occurrence of the former. Adult social reinforcement changes the pattern and not the rate of infant vocal responding.     

Infant-adult vocal interaction dynamics depend on infant vocal type,child-directedness of adult speech,and timeframe

This study explored the temporal contingencies between infant and adult vocalizations as a function of the type of infant vocalization, whether adult caregivers’ vocalizations were infant-directed or other-directed, and the timescale of analysis. We analyzed excerpts taken from day-long home audio recordings that were collected from nineteen 12- to 13-month-old American infants and their caregivers using the LENA system. Three 5-minute sections having high child vocalization rates were identified within each recording and coded by trained researchers. Infant and adult vocalizations were sequenced and defined as contingent if they occurred within 1 s, 2 s, or 5 s of each other. When using 1 s or 2 s definitions of temporal adjacency, infant vocalizations generally predicted subsequent infant-directed adult vocalizations. A reflexive vocalization (i.e. a cry or a laugh) was the strongest predictor. Likewise, within 1–2 s timeframes, infant-directed adult speech generally predicted infant vocalizations with reflexive vocalizations being particularly predictive. Infant vocalizations predicted fewer subsequent other-directed adult vocalizations and were less likely following other-directed adult vocalizations when considering up to 5 s lags. This suggests an understudied communicative role for infants of non-infant-directed adult speech. These results demonstrate the importance of timescale in studying infant-adult interactions, support the communicative significance of reflexive infant vocalizations and other-directed adult speech in addition to more commonly studied vocalization types, and highlight the challenges of determining direction(s) of influence when using only two-event sequences.     

Social regulatory effects of infant nondistress vocalization on maternal behavior

This study investigated the social regulatory function of infant nondistress vocalization in modulating maternal response. Thirteen infants and their mothers were observed weekly in a face-to-face interaction situation from 4 to 24 weeks. After the occurrences and the speech quality of infant nondistress vocalization were identified, maternal contingent responses to these vocalizations were also coded. Each responsive action was further classified by the change processes involved. Results showed that it was the occurrence of infant nondistress vocalization rather than its speech quality that regulated maternal verbal response concurrently and that infant nondistress vocalization was more likely to be synchronized with maternal facial expression and touch than with head movements. Developmentally, significant individual differences were found in the linear growth patterns of overall maternal response and within the individual modalities when responding to speechlike vocalizations.     

Key pecking of pigeons under variable-interval schedules of briefly signaled delayed reinforcement: effects of variable-interval value.

Key pecking of 4 pigeons was maintained under a multiple variable-interval 20-s variable-interval 120-s schedule of food reinforcement. When rates of key pecking were stable, a 5-s unsignaled, nonresetting delay to reinforcement separated the first peck after an interval elapsed from reinforcement in both components. Rates of pecking decreased substantially in both components. When rates were stable, the situation was changed such that the peck that began the 5-s delay also changed the color of the keylight for 0.5 s (i.e., the delay was briefly signaled). Rates increased to near-immediate reinforcement levels. In subsequent conditions, delays of 10 and 20 s, still briefly signaled, were tested. Although rates of key pecking during the component with the variable-interval 120-s schedule did not change appreciably across conditions, rates during the variable-interval 20-s component decreased greatly in 1 pigeon at the 10-s delay and decreased in all pigeons at the 20-s delay. In a control condition, the variable-interval 20-s schedule with 20-s delays was changed to a variable-interval 35-s schedule with 5-s delays, thus equating nominal rates of reinforcement. Rates of pecking increased to baseline levels. Rates of pecking, then, depended on the value of the briefly signaled delay relative to the programmed interfood times, rather than on the absolute delay value. These results are discussed in terms of similar findings in the literature on conditioned reinforcement, delayed matching to sample, and classical conditioning.     

Operant and nonoperant vocal responding in the mynah: Complex schedule control and deprivation-induced responding

Several recent studies have been concerned with operant responses that are also affected by nonoperant factors, (e.g., biological constraints, innate behavior patterns, respondent processes). The major reason for studying mynah vocal responding concerned the special relation of avian vocalizations to nonoperant emotional and reflexive systems. The research strategy was to evaluate operant and nonoperant control by comparing the schedule control obtained with the vocal response to that characteristic of the motor responses of other animals. We selected single, multiple, and chain schedules that ordinarily produce disparate response rates at predictable times. In multiple schedules with one component where vocal responding (“Awk”) was reinforced with food (fixed-ratio or fixed-interval schedule) and one where the absence of vocal responding was reinforced (differential reinforcement of other behavior), response rates never exceeded 15 responses per minute, but clear schedule differences developed in response rate and pause time. Nonoperant vocal responding was evident when responding endured across 50 extinction sessions at 25% to 40% of the rate during reinforcement. The “enduring extinction responding” was largely deprivation induced, because the operant-level of naive mynahs under food deprivation was comparable in magnitude, but without deprivation the operant level was much lower. Food deprivation can induce vocal responding, but the relatively precise schedule control indicated that operant contingencies predominate when they are introduced.     

The role of the response-reinforcer relation in delay-of-reinforcement effects

The role of the response-reinforcer relation in maintaining operant behavior under conditions of delayed reinforcement was investigated by using a two-operandum (i.e., two-key) procedure with pigeons. Responding on one key was reinforced under a tandem variable-interval differential-reinforcement-of-other-behavior (tandem VI DRO) schedule. The schedule defined a resetting unsignaled delay-of-reinforcement procedure in that a response was required when the interfood interval of the VI schedule lapsed, but further responding during the DRO component on either key reset the time interval. This ensured a fixed delay duration between any response and reinforcement. Responding on another key, physically identical to the first one except for spatial location, otherwise was without consequence. The location of the key correlated with the delay-of-reinforcement procedure varied between sessions according to a semirandom sequence. Differences in response rates between the two keys were greater, with proportionally higher rates on the key correlated with the delay-of-reinforcement procedure, the longer the delay-of-reinforcement procedure remained correlated with the same key. Differences in responding on the two keys also increased within individual sessions. These results suggest that the response-reinforcer relation is the primary determinant of responding when responding is acquired and maintained with delayed reinforcement.     

The infant vocal-conditioning literature: a theoretical and methodological critique

Most studies of operant conditioning of infant vocalization do not fully use the experimental-analysis-of-behavior methodology that behavioral researchers have developed to study operant phenomena. This could be a contributing factor in their failure to correctly operationalize the definition of reinforcement, severely limiting the amount of information they can provide about operant learning in infants. Furthermore, single-subject-design studies may be added to supplement or replace group experimental designs in the study of infant vocal conditioning if we are to recognize the different learning processes that affect infant learning. Finally, single-subject experimental designs may be crucial to the development of an effective technology of early language intervention.     

Using progressive ratio schedules to evaluate tokens as generalized conditioned reinforcers

The properties of operant reinforcers are dynamic and dependent on a number of variables, such as schedule and effort. There has been sparse research on the generalized conditioned properties of token reinforcement. We evaluated leisure items, edible items, and tokens using a progressive ratio schedule with three children with diagnoses of ASD and developmental delays. The highest break points occurred during the token reinforcement condition for two out of three participants, but response rates tended to be higher with edibles. We then evaluated the effects of presession access to edibles on the break points of edible items and tokens with two participants. Break points decreased only in the edible reinforcement condition, and the participants chose to work for leisure items rather than edibles when presession access to edibles was in place. These findings suggest that the tokens functioned as generalized conditioned reinforcers.     

A comparison of dense-to-lean and fixed lean schedules of alternative reinforcement and extinction

Behavior-reduction interventions typically employ dense schedules of alternative reinforcement in conjunction with operant extinction for problem behavior. After problem behavior is reduced in the initial treatment stages, schedule thinning is routinely conducted to make the intervention more practical in natural environments. In the current investigation, two methods for thinning alternative reinforcement schedules were compared for 3 clients who exhibited severe problem behavior. In the dense-to-lean (DTL) condition, reinforcement was delivered on relatively dense schedules (using noncontingent reinforcement for 1 participant and functional communication training for 2 participants), followed by systematic schedule thinning to progressively leaner schedules. During the fixed lean (FL) condition, reinforcement was delivered on lean schedules (equivalent to the terminal schedule of the DTL condition). The FL condition produced a quicker attainment of individual treatment goals for 2 of the 3 participants. The results are discussed in terms of the potential utility of using relatively lean schedules at treatment outset.     

The origin of language and relative roles of voice and gesture in early communication development

Both vocalization and gesture are universal modes of communication and fundamental features of language development. The gestural origins theory proposes that language evolved out of early gestural use. However, evidence reported here suggests vocalization is much more prominent in early human communication than gesture is. To our knowledge no prior research has investigated the rates of emergence of both gesture and vocalization across the first year in human infants. We evaluated the rates of gestures and speech-like vocalizations (protophones) in 10 infants at 4, 7, and 11 months of age using parent-infant laboratory recordings. We found that infant protophones outnumbered gestures substantially at all three ages, ranging from >35 times more protophones than gestures at 3 months, to >2.5 times more protophones than gestures at 11 months. The results suggest vocalization, not gesture, is the predominant mode of communication in human infants in the first year.     

Resistance to the response-decrementing effects of response-independent reinforcement produced by delay and non-delay schedules of reinforcement

In two experiments, animals were initially exposed to response-dependent schedules of food before exposure to response-independent reinforcement matched for overall rate and temporal distribution of reinforcers to the preceding condition. In Experiment I, response decrements during the response-independent phase were smaller after delayed reinforcement training than after a comparable immediate reinforcement schedule, for both doves and rats. In Experiment II variable-interval and variable-ratio schedules, both with either immediate or delayed reinforcement, were used with rats. Both the delayed reinforcement schedules produced resistance to subsequent response-independent reinforcement, but response decrements were larger after either of the immediate reinforcement conditions. It was concluded that the critical factor in response maintenance under response-independent reinforcement was the type of response-reinforcer contiguities permitted under the response-dependent schedule rather than perception of response-reinforcer “contingencies”. If the response-dependent schedule was arranged so that behaviours other than a designated operant (key pecking or lever pressing) could be contiguous with food, responding was maintained well under response-independent schedules.