Determinants of associative response latency

The relationship between single-word, free-association response latency and the following characteristics of Kent-Rosanoff words were examined: ( a ) grammatical form class, ( b ) emotionality, ( c ) familiarity, and ( d ) D (the number of different response words given to a stimulus word in a single-word free-association situation by a group of subjects). In addition was examined the relationship between response latency and ( e ) the type of associative linkage constituted by the stimulus-response combination, and ( f ) response frequency. Given the limits posed by the present stimulus material, subject material, and analyses performed, the conclusion was reached that single-word, free-associative response latency is related primarily to D ( r =0.81), secondly to the frequency with which a given stimulus-response combination occurs in a group of subjects.     

Semantic meaning and associative responding

Abstract.— The hypothesis tested was that the search for a response word in a single word, free association situation proceeds in the direction of decreasing semantic similarity between the stimulus and response words. Semantic features were assigned to the 50 first Kent-Rosanoff words and each of the three most frequent response words to each stimulus word, obtained in a single word, free association situation (N =176). An index for the number of semantic features shared by the stimulus and response words was found to decrease with increasing response latency, thus confirming the hypothesis. The findings further supports the assumption that semantic meanings of stimulus and response words are determinants of free. associative responding.     

Auditory event related potentials during lexical categorization in the oddball paradigm.

Event related potentials (ERPs) and reaction times (RTs) were recorded from 18 subjects, performing lexical categorization of words and nonwords. Three sets of monosyllable utterances, differentiated in semantic and rhyming attributes, were presented using the "oddball paradigm." ERPs included a sustained negativity which began approximately 100 msec after stimulus onset and peaked at approximately 400 mses (SN4) poststimulus, in response to target as well as to nontarget word stimuli. Semantic effects on SN4 latency were observed only for target utterances. Nonmeaningful word targets were associated with longer SN4 peak latencies as well as slower RTs compared to meaningful word targets. It is suggested that these longer latencies are due to a longer time required for an exhaustive search in permanent memory before categorizing a stimulus as a nonmeaningful word.     

Neural representation of consciously imperceptible speech sound differences

The concept of subliminal perception has been a subject of interest and controversy for decades. Of interest in the present investigation was whether a neurophysiologic index of stimulus change could be elicited to speech sound contrasts that were consciously indiscriminable. The stimuli were chosen on the basis of each individual subject's discrimination threshold. The speech stimuli (which varied along an F3 onset frequency continuum from /da/ to /ga/) were synthesized so that the acoustical properties of the stimuli could be tightly controlled. Subthreshold and suprathreshold stimuli were chosen on the basis of behavioral ability demonstrated during psychophysical testing. A significant neural representation of stimulus change, reflected by the mismatch negativity response, was obtained in all but 1 subject in response to subthreshold stimuli. Grand average responses differed significantly from responses obtained in a control condition consisting of physiologic responses elicited by physically identical stimuli. Furthermore, responses to suprathreshold stimuli (close to threshold) did not differ significantly from subthreshold responses with respect to latency, amplitude, or area. These results suggest that neural representation of consciously imperceptible stimulus differences occurs and that this representation occurs at a preattentive level.     

The effects of stimulus movement and attention on peripheral stimulus localization by 8- to 26-week-old infants

This study examined the effect of stimulus movement on localization probability and latency during attention and inattention. Forty infants, 10 each at 8, 14, 20, and 26 weeks of age were presented with a central stimulus. Then, a peripheral stimulus was presented (static or dynamic checkerboard). Stimulus movement did not affect localization probability. Infants localized the dynamic peripheral stimulus more quickly than the static peripheral stimulus when there was no focal stimulus. Focal stimulus attention attenuated this difference in localization latency between static and dynamic stimuli. Signal detection analysis showed that sensitivity to the peripheral stimulus increased over this age range along with a decrease in the bias against responding. The effects of attention were on response bias rather than stimulus sensitivity. These results imply attention affected the localization response to the peripheral stimulus but did not affect the sensitivity of the sensory and perceptual pathways to peripheral stimuli.     

On the automaticity of emotion processing in words and faces: event-related brain potentials evidence from a superficial task

The degree to which emotional aspects of stimuli are processed automatically is controversial. Here, we assessed the automatic elicitation of emotion-related brain potentials (ERPs) to positive, negative, and neutral words and facial expressions in an easy and superficial face-word discrimination task, for which the emotional valence was irrelevant. Both emotional words and facial expressions impacted ERPs already between 50 and 100 ms after stimulus onset, possibly reflecting rapid relevance detection. Following this initial processing stage only emotionality in faces but not in words was associated with an early posterior negativity (EPN). Therefore, when emotion is irrelevant in a task which requires superficial stimulus analysis, automatically enhanced sensory encoding of emotional content appears to occur only for evolutionary prepared emotional stimuli, as reflected in larger EPN amplitudes to faces, but not to symbolic word stimuli.     

Interaction Between Visually and Kinesthetically Triggered Voluntary Responses

A voluntary motor response that is prepared in advance of a stimulus may be triggered by any sensory input. This study investigated the combination of visual and kinesthetic inputs in triggering voluntary torque responses. When a visual stimulus was presented alone, subjects produced a fast and accurate increase in elbow flexion torque. When a kinesthetic stimulus was presented instead of the visual stimulus, subjects produced a similar response with a reduced response latency. When a visual stimulus was presented in combination with a kinesthetic stimulus, subjects initiated their responses after either a visual or a kinesthetic response latency, depending on the relative timing of the two stimuli. An analysis of response amplitude suggested that when visual and kinesthetic stimuli were combined, both stimuli triggered a response. The results are more consistent with a simple behavioral model of addition of visual and kinesthetic responses (which predicts that the response to combined stimuli should be the sum of individual responses) than with a model of exclusion of one response (which predicts that the response to combined stimuli should be identical to either the visual or the kinesthetic response). Because addition of visually and kinesthetically triggered responses produced a response with an erroneously large amplitude, it is suggested that visual and kinesthetic inputs are not always efficiently integrated.     

Rate of response as a visual social stimulus

In Exp. 1, a high rate of responding (chain pulling) of a stimulus monkey was established as a visual positive discriminative stimulus for the operant behavior (bar pressing) of an observer monkey. The terminal performance of the observer under conditions in which a high rate of response of the stimulus monkey alternated in a variable temporal arrangement with a zero rate of response of the stimulus monkey (negative discriminative stimulus) was essentially the same as when nonbehavioral stimuli are correlated with the availability of reinforcement. By manipulating the schedule of reinforcement to change the rate of responding of the stimulus subject without changing its rate of reinforcement, Exp. 2 showed that the effective behavioral stimulus for the observer was the rate of chain pulling by the stimulus subject. A novel intermediate rate of responding by the stimulus monkey resulted in an intermediate rate (generalization) on the part of the observer during an extinction test. These experiments demonstrated that the rate of responding of one organism can function as a discriminative stimulus to control the rate of responding of another organism; and that the rate of responding is similar to other physical stimuli in terms of discrimination and generalization.     

Interaction between visually and kinesthetically triggered voluntary responses

A voluntary motor response that is prepared in advance of a stimulus may be triggered by any sensory input. This study investigated the combination of visual and kinesthetic inputs in triggering voluntary torque responses. When a visual stimulus was presented alone, subjects produced a fast and accurate increase in elbow flexion torque. When a kinesthetic stimulus was presented instead of the visual stimulus, subjects produced a similar response with a reduced response latency. When a visual stimulus was presented in combination with a kinesthetic stimulus, subjects initiated their responses after either a visual or a kinesthetic response latency, depending on the relative timing of the two stimuli. An analysis of response amplitude suggested that when visual and kinesthetic stimuli were combined, both stimuli triggered a response. The results are more consistent with a simple behavioral model of addition of visual and kinesthetic responses (which predicts that the response to combined stimuli should be the sum of individual responses) than with a model of exclusion of one response (which predicts that the response to combined stimuli should be identical to either the visual or the kinesthetic response). Because addition of visually and kinesthetically triggered responses produced a response with an erroneously large amplitude, it is suggested that visual and kinesthetic inputs are not always efficiently integrated.     

Conditioned reinforcement and discrimination performance

Pigeons were trained in a three-key chamber to peck one side key in the presence of a vertical line on the center key and to peck the other side key in the presence of a horizontal line. Correct choice responses were reinforced with food according to fixed- and variable-ratio, fixed-interval, and differential-reinforcement-of-long-latency schedules of reinforcement. For each schedule, the birds performed under each of two conditions: (1) each correct choice response produced a brief presentation of stimuli intermittently paired with food, then the next trial; (2) each correct choice response produced an intertrial interval only. For all schedules except one long latency schedule, response rates were higher under the condition of brief stimulus presentation than under the comparable control condition. Presentation of brief magazine stimuli increased choice accuracy. The amount of change in accuracy was correlated with the rate of food presentation. Performance under the schedules with highest food reinforcement rates showed no enhancement; performance under the schedules with the lowest reinforcement rates showed the greatest enhancement.     

Complexity,response competition,and preference

In an attempt to resolve disagreements about the events underlying repeated exposure to a stimulus and the affective consequences of these events, two experiments examined psychological complexity and response competition (two measures of the uncertainty produced by a stimulus) as related to each other and to liking and goodness of meaning ratings of Chinese characterlike stimuli. In Experiment 1, 60 undergraduates' mean latency of first free association to the stimuli (response competition) increased as a perfect monotonic function of the number of lines constituting them (psychological complexity). In Experiment 2, ratings of liking by 40 undergraduates were highest for stimuli associated with an intermediate level of uncertainty (psychological complexity and response competition). Thus it was speculated that a moderate number of stimulus exposures (reducing uncertainty to an intermediate level) is preferable to an indefinitely large number of exposures (reducing uncertainty to a minimal level). The finding of no relationship between rated goodness of stimulus meaning and uncertainty was judged to be consistent with Stang's (1974) hypothesis that characteristically observed increases in rated goodness with increasing stimulus exposures (decreasing uncertainty) are a result of subject intuitions rather than an effect of decreasing uncertainty.     

Brainstem frequency-following response recorded from one vertical and three horizontal electrode derivations

The human brainstem frequency-following response reflects neural activity to periodic auditory stimuli. Responses were simultaneously recorded from one vertically oriented and three horizontally oriented electrode derivations. Nine participants each received a total of 16,000 tone repetitions, 4,000 for each of four stimulus frequencies: 222, 266, 350, and 450 Hz. The responses were digitally filtered, quantified by correlation and spectral analysis, and statistically evaluated by repeated measure analysis of variance. While the various horizontal derivation responses did not differ from each other in latency (values tightly clustered around M= 2.60 msec.), the vertical derivation response occurred significantly later (M=4.38 msec.). The smaller latency for the horizontal responses suggests an origin within the acoustic nerve, while the larger latency for the vertical response suggests a central brainstem origin. The largest response amplitude resulted from gold "tiptrode" electrodes placed in each auditory meatus, suggesting that this electrode derivation provided the most accurate (noninvasive) assessment of short-latency events originating at the level of the auditory nerve.     

A STIMULUS CONTROL PROCEDURE TO DECREASE MOTOR AND VOCAL STEREOTYPY

A changing criterion design was used to examine the effects of two stimuli (a green card and a red card), conditioned via discrimination training, on reducing motor and vocal stereotypy in a youngster with autism while he looked at books. During discrimination training, motor and vocal stereotypy was not interrupted in the presence of a green stimulus, but was interrupted in the presence of a red stimulus using manual guidance and appropriate behavior was reinforced. After the participant demonstrated successful discrimination of the stimuli (i.e., the absence of stereotypy in the presence of a red stimulus and the engagement in stereotypy in the presence of a green stimulus), intervention began. During intervention, upon meeting criterion for latency to engage in motor and vocal stereotypy in the presence of the red stimulus for a target duration, the participant was provided access to the green stimulus, which signaled that motor and vocal stereotypy would not be interrupted. The criterion latency to engage in stereotypy in the presence of the red stimulus was systematically increased. Simultaneously, the duration of access to the green stimulus was systematically decreased. The red and green stimuli were faded from poster boards to colored 10 × 10 cm cards, and stimulus control was generalized to the participant's classroom and to a community setting (i.e., public library). Results are discussed in terms of discrimination training as a useful intervention for reducing motor and vocal stereotypy. Copyright © 2011 John Wiley & Sons, Ltd.     

On the discriminative control of concurrent responses: the relations among response frequency, latency, and topography in auditory generalization

Human subjects were used in a study of auditory generalization following multiple-response discrimination training. The relations observed among stimulus intensity, response probability, and response latency were invariant with respect to whether the two vocal responses conditioned were topographically discrete, as in one experiment, or topographically continuous, as in another. The major findings were:

1. The probabilities associated with a specific response were maximal over several stimulus values at the extreme ends of the continuum, then dropped sharply at stimuli intermediate to the initial S^D's as the probability of the alternative response increased.

2. Overall response latency was inversely related to the relative frequency of the two responses at each stimulus value. When the two responses were most nearly equal in probability, latencies were maximal; when one response had close to unit or zero probability, latencies were minimal.

3. Analysis of the latencies of the two responses, taken separately, revealed: (a) an increase in latency as the difference between the test stimulus and the initial S^D increased; (b) a sharp discontinuity in the latency gradient and reversal in trend at intermediate stimulus intensities; and (c) at a given stimulus value, latencies associated with the stochastically dominant response were consistently shorter than those of the nondominant response.

4. No changes in response topography (fundamental frequency) were correlated with the characteristic changes in probability and latency during stimulus generalization.

     

Effects of differences between stimuli, responses, and reinforcer rates on conditional discrimination performance

In a discrete-trial conditional discrimination procedure, 4 pigeons obtained food reinforcers by pecking a key with a short latency on trials signaled by one stimulus and by pecking the same key with a long latency on trials signaled by a second stimulus. The physical difference between the two stimuli and the temporal separation between the latency values required for reinforcement were varied factorially over four sets of conditions, and the ratio of reinforcer rates for short and long latencies was varied within each set of conditions. Stimulus discrimination varied directly with both stimulus and response differences and was unaffected by the reinforcer ratio. Sensitivity to reinforcement, estimated by generalized-matching-law fits to the data within each set of conditions, varied directly with the response difference but inversely with the stimulus difference arranged between sets of conditions. Because variations in stimulus differences, response differences, and reinforcer differences did not have equivalent effects, these findings question the functional equivalence of the three terms of the discriminated operant: antecedent stimuli, behavior, and consequences.     

SENSORY AND PREPARATORY FACTORS IN RESPONSE LATENCY: III. Preknowledge and regularity of stimuli as antecedent variables

T hrane , V. C. Sensory and preparatory factors in response latency. III. Preknowledge and regularity of stimuli as antecedent variables. Scand. J. Psychol ., 1961, 2, 30–44.—Interaction between stimulus and organismic determinants of simple reaction time under weak and strong auditory stimulation was studied with 24 subjects. Results indicate that without specific preknowledge of the stimulus variants presented, there is little or no correlation between sensory and non-sensory determinants of response latency, but that both speed and constancy of response are influenced by preknowledge, and to some extent by regularity of stimuli, in a manner and to a degree which depend on the expected intensity, thus being consistent with the hypothesis of bipolar (positive and negative) compensatory interaction.     

Personality and the topography of the conditioned eyelid response

One-hundred and four women were tested on an eyelid conditioning paradigm in a 2 x 2 x 2 factorial design where two levels of US intensity (1 vs 3 p.s.i.) were balanced against two rest pause interpolations (after 25 and after 50 trials), and the presence or absence of a warning stimulus prior to CS-US presentation. Subjects were later classified as high, low or intermediate extraverts on the basis of a personality questionnaire. A very detailed analysis of conditioned responses was carried out, using both simple and composite measures including work-ratio, utility-ratio, CR frequency, peak latency, peak amplitude, response area and effective response area, degree of avoidance amplitude and latency, etc. Major findings related to similar effects of high intensity US vs low intensity US, and introversion vs extraversion; introverts react as if they were responding to more intense stimuli than extraverts. This finding cuts across other parameter variables, and supports Eysenck's formulation of personality-conditioning relationships in terms of higher cortical arousal in introverts as compared with extraverts.     

Event-related potential sensitivity to acoustic and semantic properties of terminal words in sentences.

This experiment was concerned with the effects of phonologically correct masking on the electrophysiological responses to terminal words of spoken sentences differing in contextual constraint. Two event-related potential (ERP) components, the N400 and N200, were recorded to the terminal words of high and low constraint sentences in four conditions. In the Control condition, subjects (Ss) simply attended to the sentences with no explicit task instructions. In the Semantic condition, Ss were required to listen to the stimuli in order to make semantic judgements about the terminal word of each sentence. The Control+Masking condition was identical to the Control condition except for the simultaneous presentation of a masking stimulus. The Semantic+Masking condition had Ss listening to sentences in the presence of masking with the task of making semantic judgements about the terminal word of each sentence. ERPs were recorded from Fz, Cz, Pz, T3, and T4 in 10 subjects. Amplitudes of both the N200 and the N400 were sensitive to contextual constraint with larger responses elicited by the terminal words of low constraint sentences. In addition to demonstrating the co-occurrence of the N200 and N400, this experiment highlighted a functional separation between the two components. Masking had no statistically significant effect on N200 latency but N400 latency was delayed in the masked conditions relative to those in the unmasked conditions. It is proposed that the N200 and N400 are manifestations of two different processes; the N200 reflects the acoustic/phonological processing of the terminal word while the N400 reflects the cognitive/linguistic processing. The relationship between the N200 recorded in this experiment and the discrimination N200 is discussed.     

Contextual dependencies in predictive learning

Two experiments assessed contextual dependencies in a predictive-learning task. Subjects learned to associate each of four pictorial stimuli with the occurrence or non-occurrence of a specific outcome. Each of these stimuli, the intentional stimuli, was presented against one of two different visual (Experiment 1) or auditory (Experiment 2) context stimuli. These context stimuli were incidental: subjects were not explicitly instructed to pay any attention to them and each of them in isolation was not predictive of the outcome. During acquisition and testing, subjects expressed the expected relationship between intentional stimulus and outcome by an appropriate key press. At test, intentional stimuli were presented either with the same contextual stimulus as also present during acquisition (same trials), or with the other one (switched trials). The response latency was slower on switched trials than on same trials in each experiment, a result extending previous findings on the effect of environmental contextual stimuli on task performance. Results are discussed in the framework of contextual occasion setting and habituation to contextual stimuli.