On the relation between recent neurobiological data on perception (and action) and the Husserlian theory of constitution

The phenomenological theory of constitution promises a solution for the problem of consciousness insofar as it changes the traditional terms of this problem by systematically correlating subject and object in the unifying context of intentional acts. I argue that embodied constitution must depend upon the role of kinesthesia as a constitutive operator. In pursuing the path of intentionality in its descent from an idealistic level of pure constitution to this fully embodied kinesthetic constitution, we are able to gain access to different ontological regions such as physical thing, owned body and shared world. Neuroscience brings to light the somatological correlates of noemata. Bridging the gap between incarnation and naturalisation represents the best way of realizing the foundational program of transcendental phenomenology.     

Stimulus properties of conspecific behavior

Two experiments identified the conditions in which the behavior of one bird acquired discriminative control of the behavior of a second bird. The schedule-controlled behaviors of the “stimulus” bird were differentially correlated with the components of a multiple schedule according to which the pecking of an “experimental” bird produced food. In Experiment 1, three pairs of pigeons acquired a successive discrimination and two reversals with the conspecific stimuli. Experiment 2 included a control condition in which no systematic relationship existed between the conspecific stimuli and the component schedules. While differential responding during the components of the multiple schedule was again found when the conspecific stimuli were available, differential responding did not occur in the control condition. Test conditions included in the experiments indicated that (a) the differential responding was not dependent on the discriminative properties of reinforcement, (b) the pecking of the stimulus and experimental birds was temporally interrelated, (c) the visual conspecific stimuli were critical to the maintenance of the discrimination, and (d) the observed stimulus control immediately generalized to an unfamiliar conspecific.     

Choice in a "self-control" paradigm: effects of a fading procedure

Pigeons chose between an immediate 2-second reinforcer (access to grain) and a 6-second reinforcer delayed 6 seconds. The four pigeons in the control group were exposed to this condition initially. The four experimental subjects first received a condition where both reinforcers were delayed 6 seconds. The small reinforcer delay was then gradually reduced to zero over more than 11,000 trials. Control subjects almost never chose the large delayed reinforcer. Experimental subjects chose the large delayed reinforcer significantly more often. Two experimental subjects showed preference for the large reinforcer even when the consequences for pecking the two keys were switched. The results indicate that fading procedures can lead to increased “self-control” in pigeons in a choice between a large delayed reinforcer and a small immediate reinforcer.     

Multiple and concurrent schedule performance: independence from concurrent and successive schedule contexts

Six pigeons were trained on multiple variable-interval schedules and performance was measured in the presence or absence of another variable-interval schedule (the common schedule) arranged concurrently with both components. Manipulations included varying the rate of reinforcement on the common schedule, leaving the common schedule unchanged while the components of the multiple schedule were varied, varying the multiple schedule components in the absence of the common schedule, and varying one component of the multiple schedule while the other component and the common schedule were unchanged. The normal rate-increasing and rate-decreasing effects of reinforcement rate increase were found, except that changing one multiple schedule component did not affect the response rate in the successively available common schedule component. Both concurrent and multiple schedule performance undermatched obtained reinforcement-rate ratios, but the degree of undermatching in multiple schedules was reliably greater. Allocation of responses between multiple schedule components was unaffected by the concurrent availability of reinforcement, and allocation of responses between concurrent schedules was unaffected by the successive availability of different reinforcement rates.     

Parameters affecting the maintenance of negatively reinforced key pecking

Three negative reinforcement experiments employing a key-peck response are described. In Experiment I, pigeons shocked on the average of twice per minute (imposed condition) could produce, by pecking a key, an alternate condition with correlated stimuli. Delayed shocks were added, across sessions, to the alternate condition until pecking stopped. Two of three pigeons continued to peck despite a 100% increase in shock frequency. In Experiment II, pigeons were shocked in the imposed condition four times per minute. The postresponse delay to shock was held constant by delivering, in the alternate condition, the next shock, or the next two, three, or four shocks from the imposed-condition shock schedule. All three subjects continued to peck with no change in delay to the first two postresponse shocks but with a 75% reduction in shock frequency. In Experiment III, a response produced an immediate shock followed by a shock-free period. Three of four subjects continued to respond despite reduced delay to shock. Delay-to-shock or shock-frequency reduction was sufficient to maintain key pecking, but neither was necessary. The conditions that negatively reinforce the pigeon's key peck were similar to conditions that negatively reinforce the rat's bar press.     

Elicited responding in chain schedules.

An omission procedure was employed to study elicited pecking in the first component of a two-component chain schedule. Both components were fixed-interval schedules correlated with colored keylights. The first response following the initial-link schedule produced a second fixed-interval schedule. We studied several fixed-interval lengths in two conditions: a standard response-dependent condition and an omission-contingent condition. The omission-contingent condition differed from the response-dependent condition in that responses during the initial fixed interval terminated the trial (omitting the terminal component and grain). If the terminal component was not omitted, a response following the terminal link's requirement produced 4-s access to grain. Pigeons responded during more than 70% of the initial links in the omission-contingent condition and responded during more than 90% of the initial links in the response-dependent condition. In general, rates of responding were consistent with the percentage data. The responding in the omission condition suggests that there may be elicited pecking, in chain schedules using pigeons, that is not the result of contingent conditioned reinforcement.     

Graded differential reinforcement: Response-dependent reinforcer amount

After key pecking had been autoshaped, six pigeons were exposed to a condition in which the duration of grain availability at the end of an 8-second trial depended on the number of responses emitted during the trial (0.25-second access to grain per response). This procedure, called correlated reinforcement, alternated across conditions with the automaintenance baseline in which the 8-second trial terminated with a constant 2.5-second access to grain. Two control procedures were run; in both, the reinforcer durations were yoked to those obtained in the last correlated session. In the yoked control no responses were required, but in the single-response yoked control at least one response was required to receive the yoked duration. The correlated condition maintained response rates above those produced by the two control conditions. These results may be accounted for by differential reinforcement.     

Finding a home: Developmental and neurobiological perspectives on cultural models

This article looks at cultural models in the light of human development, and neurobiological findings in motivation, learning, and cognition. It is argued that at the individual level, the acquisition of cultural models relies on several innate, neurobiologically based motivational, learning, and cognitive systems. These are: (a) a primary motivation to form social bonds which is driven by affect; (b) highly specialized social learning circuits, involving, but not limited to, mirror neuron systems, that facilitate the encoding of social information through implicit, embodied, imitational learning processes; and (c) the formation of culturally based templates for behavior and cognition centered around structures, collectively known as the “default mode network,” which is essential to self‐understanding, autobiographical memory, social cognition, prospection, and theory‐of‐mind. Cultural models, it is argued, are acquired through innate motivational processes that tie the individual emotionally to a secure base of familiar people and customs. This instinctual desire for proximity to others facilitates the efficient, largely implicit, patterning of knowledge and expectations. Shared knowledge and expectations, in turn, create a common, mostly implicit or unconscious, experience of subjectivity within groups. This allows each individual to automatically and effortlessly interact with similarly enculturated others.     

Individual differences in neonatal “imitation” fail to predict early social cognitive behaviour

The influential hypothesis that humans imitate from birth – and that this capacity is foundational to social cognition – is currently being challenged from several angles. Most prominently, the largest and most comprehensive longitudinal study of neonatal imitation to date failed to find evidence that neonates copied any of nine actions at any of four time points (Oostenbroek et al., [2016] Current Biology, 26, 1334–1338). The authors of an alternative and statistically liberal post‐hoc analysis of these same data (Meltzoff et al., [2017] Developmental Science, 21, e12609), however, concluded that the infants actually did imitate one of the nine actions: tongue protrusion. In line with the original intentions of this longitudinal study, we here report on whether individual differences in neonatal “imitation” predict later‐developing social cognitive behaviours. We measured a variety of social cognitive behaviours in a subset of the original sample of infants (N = 71) during the first 18 months: object‐directed imitation, joint attention, synchronous imitation and mirror self‐recognition. Results show that, even using the liberal operationalization, individual scores for neonatal “imitation” of tongue protrusion failed to predict any of the later‐developing social cognitive behaviours. The average Spearman correlation was close to zero, mean r_s = 0.027, 95% CI [?0.020, 0.075], with all Bonferroni adjusted p values > .999. These results run counter to Meltzoff et al.'s rebuttal, and to the existence of a “like me” mechanism in neonates that is foundational to human social cognition.     

Brief presentations are sufficient for pigeons to discriminate arrays of same and different stimuli

Four pigeons first learned to discriminate 16-item arrays of same from different pictorial stimuli. They were then tested with reduced exposure to the pictorial arrays, brought about by changes in the stimulus viewing requirement under fixed-ratio (FR) and fixed-interval (FI) schedules. Increasing the FR requirement enhanced discriminative performance up to 10 pecks; increasing the FI requirement enhanced discriminative performance up to 5 s. Exposures to the stimulus arrays averaging only 2 s supported reliable discrimination. Pigeons thus discriminate same from different stimuli with considerable speed, suggesting that same-different discrimination behavior is of substantial adaptive significance.