Reaction time as a function of stimulus intensity for the monkey

Monkeys were trained to release a telegraph key in response to a visual or auditory stimulus. The latency of the key release response was measured for different stimulus intensities. In general, the relation between latency and intensity is inverse and exponential with greater variability of latency at the lower intensities. Some preliminary data involving differential reinforcement of short latencies are presented.     

Reaction time to a second stimulus as a function of intensity of the first stimulus

Reaction time (RT) to the second of two stimuli presented in rapid succession was examined as a function of the intensity of the first stimulus (S₁). It was found that the delay in RT₂ was greater following a dim first stimulus than following a bright first stimulus. The magnitude of this increase corresponded to the difference in RTs to the two intensity levels of S₁. These results support the prediction of a single channel model of response selection. Examination of mean first RTs revealed a general elevation in latency of RT. However, since this increase was not influenced by the inter-stimulus interval (ISI) or by the intensity of the second stimulus (S₂), and since the same increase was found on “catch trials“ where no S₂ was presented, this increase is considered to be a function of change in set in the double response situation.     

Critical fusion frequency as a function of stimulus intensity: and wavelength composition

Six Ss made judgments of equal loudness by adjusting the intensity of comparison tones of 10 different frequencies. The comparison tones were presented diotically alternately with standaxd tones. Each standard tone remained fixed at one frequency (125, 1,000, or 8,000 Hz) and one intensity (10, 20, 40, or 70 dB sensation level)while collecting the data for any single equal-loudness contour. In this manner, families of equal-loudness contours were generated for each of the three standard frequencies. The contours for the 1,000-Hz standard were compared with those in the literature. The families of contours for the 125- and 8,000-Hz standards, determined by the same algorithm, differed in the spacing of the contours from the 1,000-Hz standard family as well as from each other. Implications for the reflexive, symmetric, and transitive properties of the equal-loudness relation axe discussed.     

Differential responding as a function of auditory stimulus intensity without differential reinforcement

Two groups of four rats each were trained to bar press on a variable-interval 2-min schedule. During training, either 3, 5, or 9 auditory stimuli of various intensities were randomly presented. A direct relationship between stimulus intensity and rate of responding was obtained, but it was more consistent in the group trained initially with three stimuli than for the group that started with nine stimuli. The results are related to the concept of stimulus intensity dynamism and the necessary conditions for the acquisition of stimulus control.     

Discrimination learning as a function of stimulus location along an auditory intensity continuum

Eight groups of rats were trained on an auditory intensity discrimination in which the discriminative stimuli were separated by 10 decibels (db). Four pairs of stimuli were selected from different regions along a 60–100 db (SPL) intensity continuum. Counterpart groups were trained on each stimulus pair, with the relative intensity positions of the reinforced stimulus (S^D) and the non-reinforced stimulus (S^Δ) reversed for the two groups. Discrimination acquisition curves were compared to determine whether stimuli separated by equal logarithmic units were of comparable “difficulty”, and to determine the relative effectiveness of an S^D serving as the more versus less intense member of a stimulus pair. It was concluded that: (1) When S^D is the more intense, auditory intensities of constant logarithmic separation are graded in “difficulty” along the intensity continuum; high intensity discriminative stimuli are most readily discriminated. When S^Δ is the more intense, this graded effect is not evident. (2) For a given continuum location, discrimination is inferior when S^Δ is the more intense. This effect is most pronounced at the high intensity end of the continuum and is chiefly attributable to differences in the rate of S^Δ responding.     

Reinforced stimulus preexposure effects as a function of US intensity: Implications for understanding the Hall-Pearce effect

Three conditioned suppression experiments examined the Hall-Pearce (1979) negative transfer effect in rats. Experiment 1 replicated the effect: CS-US_weak pairings retarded subsequent fear conditioning to the CS as a result of CS-US_strong pairings. The size of this retardation was less than that produced by non-reinforced CS presentations (latent inhibition). When the magnitude of the US_weak was reduced in Experiment 2, the Hall-Pearce effect was greater than latent inhibition. Experiment 3 confirmed the findings of the two previous experiments, and demonstrated that magnitude of the Hall-Pearce negative transfer effect is inversely related to the magnitude of the US_weak. From these findings it is suggested that the Hall-Pearce effect consists of a balance between a positive transfer of associative strength, and negative transfer based on CS- and US-preexposure effects.     

Hue discrimination as a function of stimulus luminance

The relation between hue discrimination and stimulus luminance was investigated. It was found that discrimination was best at the highest luminance and deteriorated at the lowest, except in the yellow region.