Classical eyeblink conditioning in adulthood: effects of age and interstimulus interval on acquisition in the trace paradigm

Effects of age and interstimulus interval (ISI) were examined in eyeblink classical conditioning with a trace paradigm. Sixty young adults were trained in Experiment 1 with 6 interstimulus intervals (ISIs): 400, 900, 1,200, 1,500, 1,800, and 2,100 ms. The purpose was to find an ISI value for humans that would result in nonoptimal acquisition. ISIs of 1,200 ms and longer were nonoptimal. Adults aged 17-81 years were trained in Experiment 2 with a nonoptimal 1,800-ms ISI in the trace paradigm. Young and middle-aged subjects demonstrated equivalent levels of acquisition, and only older subjects conditioned more poorly. Aging appears to affect conditioning in the long-ISI trace paradigm as well as in the short-ISI delay paradigm.     

Inhibition of return in visual marking? The importance of the interstimulus interval and the type of search task

Four experiments are presented that examine the possibility that inhibition of return (IOR) may occur in visual marking. Previously, Watson and Humphreys (1997), using a cue duration of 750 ms and an interstimulus interval (ISI) of 250 ms, concluded that IOR was not present in visual marking. In the present study, the first experiment examined three ISIs (250 ms, 500 ms, and 750 ms) with a constant stimulus onset asynchrony (SOA, 1000 ms) in a typical cueing paradigm and failed to find IOR with the short ISI. Based on these findings, the second (feature search) and third (conjunction search) experiments tested for IOR by using a visual marking paradigm with a 500 ms ISI. Evidence for IOR was found in the feature search (preview condition similar to half-elements baseline condition) and not in the conjunction search (preview condition similar to the all-elements baseline). The typical preview effect was found in Experiment 4 with a cue duration 1000 ms and no ISI. Overall, these findings indicate that IOR may play a role in visual marking, but only with feature search tasks and long ISIs between displays.     

Effects of Early Hippocampal Lesions on Trace, Delay, and Long-Delay Eyeblink Conditioning in Developing Rats

The effects of bilateral hippocampal aspiration lesions on later acquisition of eyeblink conditioning were examined in developing Long-Evans rat pups. Lesions on postnatal day (PND) 10 were followed by evaluation of trace eyeblink conditioning (Experiment 1) and delay eyeblink conditioning (Experiment 2) on PND 25. Pairings of a tone conditioned stimulus (CS) and periocular shock unconditioned stimulus (US, 100 ms) were presented in one of three conditioning paradigms: trace (380 ms CS, 500 ms trace interval, 880 ms interstimulus interval [ISI]), standard delay (380 ms CS, 280 ms ISI), or long delay (980 ms CS, 880 ms ISI). The results of two experiments indicated that hippocampal lesions impaired trace eyeblink conditioning more than either type of delay conditioning. In light of our previous work on the ontogeny of trace, delay, and long-delay eyeblink conditioning (Ivkovich, Paczkowski, & Stanton, 2000) showing that trace and long-delay eyeblink conditioning had similar ontogenetic profiles, the current data suggest that during ontogeny hippocampal maturation may be more important for the short-term memory component than for the long-ISI component of trace eyeblink conditioning. The late development of conditioning over long ISIs may depend on a separate process such as protracted development of cerebellar cortex.     

Discriminability and central intermittency in same-different judgements

Four sets of paired visual stimuli (OO, XX, XO, or OX) were judged by 48 subjects to be either “same” or “different.” Decision latencies of the same and different judgement were studied as a function of the inter-stimulus interval (ISI). In Experiments I and II, in which stimulus durations were 70 millisec., decision latencies showed marked increases when the ISI was reduced to 100 millisec., but in Experiments III and IV, in which the stimulus durations were only 40 millisec., comparable increases did not occur until the ISI was reduced to 50 millisec. These increases were more marked for “same” than for “different” judgements, although overall decision latencies were generally shorter for “same” judgements. The effects of varying ISIs and stimulus durations are interpreted in terms of masking; they fail to support an hypothesis of central intermittency.     

Auditory frequency discrimination in adult developmental dyslexics

Developmental dyslexics reportedly discriminate auditory frequency poorly. A recent study found no such deficit. Unlike its predecessors, however, it employed multiple exposures per trial to the standard stimulus. To investigate whether this affects frequency discrimination in dyslexics, a traditional two-interval same-different paradigm (2I_1A_X) and a variant with six A-stimuli per trial (2I_6A_X) were used here. Frequency varied around 500 Hz; interstimulus interval (ISI) ranged between 0 and 1,000 msec. Under 2I_1A_X, dyslexics always had larger just noticeable differences (JNDs) than did controls. Dyslexic and control JNDs were equal at shorter ISIs under 2I_6A_X, but dyslexics became worse than controls at longer ISIs. Signal detection analysis suggests that both sensory variance and trace variance are larger in dyslexics than in controls.     

Audiotactile temporal order judgments

We report a series of three experiments in which participants made unspeeded 'Which modality came first?' temporal order judgments (TOJs) to pairs of auditory and tactile stimuli presented at varying stimulus onset asynchronies (SOAs) using the method of constant stimuli. The stimuli were presented from either the same or different locations in order to explore the potential effect of redundant spatial information on audiotactile temporal perception. In Experiment 1, the auditory and tactile stimuli had to be separated by nearly 80 ms for inexperienced participants to be able to judge their temporal order accurately (i.e., for the just noticeable difference (JND) to be achieved), no matter whether the stimuli were presented from the same or different spatial positions. More experienced psychophysical observers (Experiment 2) also failed to show any effect of relative spatial position on audiotactile TOJ performance, despite having much lower JNDs (40 ms) overall. A similar pattern of results was found in Experiment 3 when silent electrocutaneous stimulation was used rather than vibrotactile stimulation. Thus, relative spatial position seems to be a less important factor in determining performance for audiotactile TOJ than for other modality pairings (e.g., audiovisual and visuotactile).     

Inhibition of return to color: A replication and nonextension of Law, Pratt, and Abrams (1995)

We presented subjects with an unpredictive cue that was followed after a 150- to 900-msec interstimulus interval (ISI) by a detection target. Cue and target were blue or red squares that appeared at fixation and in an otherwise uniform black field. In a filler condition, a task-irrelevant filler stimulus (magenta square) was presented during the ISI; in a no-filler condition, no stimulus appeared during the ISI. Using only a 900-msec ISI, Law, Pratt, and Abrams (1995) reported slower reaction times (RTs) when cue and target were the same color, but only when the task-irrelevant filler was presented during the ISI. They argued that attention is first drawn to the cue color and that inhibition of return (IOR; see Posner & Cohen, 1984) is established when attention is drawn away from that cue color representation by the task-irrelevant filler. Critical to their view is the assumption that IOR occurs only after attention is drawn away from the cue color by the filler. Assuming a time course for the withdrawal of attention from the cue color representation, Law et al. ’s view predicts growth of the inhibitory effect as a function of ISI in the filler condition as well as facilitation at early ISIs in the no-filler condition (because there is no filler to withdraw attention from the cue color). Contrary to these predictions, we found that the inhibitory effect observed by Law et al. at the 900-msec ISI was present at—and did not vary in magnitude across—the range of ISIs tested. And there was never facilitation in the no-filler condition. These results challenge Law et al. ’s inference that IOR for foveally presented colors was operating in their paradigm.     

Slow potential changes and choice reaction time as a function of interstimulus interval

Slow potential changes were recorded over the vertex (C_z) during a choice reaction task. The constant interstimulus interval (ISI) between the visual warning (S₁) and the visual imperative signal (S₂) was either 200, 400, 1000 or 2000 msec. The contingent negative variation (CNV) was not only measured between S₁ and S₂ (CNV₂), but also before S₁ (CNV₁).The main results were: (1) The CNV₂ amplitude showed significant variation as a function of ISI. It reached its maximum with an ISI of 1000 msec. (2) CNV₁ developed only before the short ISIs (200 and 400 msec). (3) When CNV₁ and CNV₂ were summed the differences in CNV amplitudes and durations between different ISIs became smaller. (4) The peak-to-peak amplitude P₁-N₁ of the potential evoked by S₁ was enhanced with short ISIs. (5) The correlations between mean CNV and median reaction time (RT) were low but significant for ISIs of 400, 1000 and 2000 msec. When, however, the effect of subjects was partialized out these correlations were drastically reduced, whereas the partialization of session and block effects had no noticeable influence on these correlations. (6) The correlations between single RT and single CNV (measured for the ISI of 1000 msec, individually for two subjects) were weak or even completely lacking.The main conclusion was that CNV coincides with preparedness to react to a stimulus in a choice RT-task, but its amplitude at the moment of onset of the imperative stimulus does not reflect, or reflects weakly, the degree of preparedness (as indicated by RTs) at that moment.     

Effects of Prime Type and Delay on Multiplication Priming: Evidence for a Dual-process Model

Two experiments investigated effects of numerical primes on production of simple multiplication facts (e.g. 4 × 8 = ?). In Experiment 1, a correct (32), related (24), unrelated (27), or neutral (##) prime appeared for 200 msec and was followed by a target problem at an ISI of 0, 750, or 1500 msec. Relative to neutral primes, correct primes produced constant RT and accuracy benefits across ISIs, and unrelated primes produced constant RT costs. Related primes produced costs compared to unrelated primes at the 0-msec ISI only. In Experiment 2, eliminating correct-answer primes from the stimulus set eliminated all the false-prime effects except the costs of related primes at the 0-msec ISI. We propose a dual-process account incorporating a familiarity-based name-the-prime strategy that produces benefits and costs insensitive to ISI and an automatic retrieval-priming process that is measurable only at short ISIs.     

Tempo sensitivity in auditory sequences: Evidence for a multiple-look model

Differential thresholds for tempi (with interonset intervals ranging from 100 to 1,500 msec) were measured using an adaptive 2IFC paradigm for several types of auditory sequences. In Experiment 1, the number of intervals in an isochronous sequence was varied to compare the sensitivity for single intervals withthat for sequences of two to six intervals. Mean relative just noticeable differences (JNDs) decreased as the number of intervals increased (single intervals=6%, two intervals=4%, four intervals=3.2%, six intervals=3%) and were optimal at intermediate tempi for both sequences and single intervals (as low as 1.5% in the range between 300 and 800 msec). In Experiment 2, the sensitivity for different types of irregular sequences was studied. Globally, JNDs for irregular sequences were of an intermediate level between that observed for single intervals and that observed for regular sequences. However, the closer a sequence was to regularity, the lower its relative JND. Experiment 3 demonstrated that musicians were more sensitive than nonmusicians to changes in tempo, and this was true for single intervals and for regular and irregular sequences, demonstrating the role of training on these abilities. The results are discussed in terms of possible underlying mechanisms, in particular those providing a mental representation of the mean and dispersion of successive interval durations.     

Attenuation of age-related conditioning deficits in humans by extension of the interstimulus interval

Young (17-22 years) and older (61-86 years) persons underwent classical conditioning of the eye-blink response to a tone conditioned stimulus (CS) and an airpuff unconditioned stimulus (UCS) at 1 of 3 interstimulus intervals (ISIs; 400, 650, and 900 ms). As in a previous study, older subjects conditioned more slowly and emitted fewer conditioned responses at the optimal 400-ms ISI. At longer ISIs, however, this age-related disruption of classical conditioning was attenuated. These differences in conditioning were not due to nonassociative factors, such as sensitivity to the tone CS or airpuff UCS or to differences in spontaneous blink rate, nor were they due to differences in general cognitive abilities. The results are discussed in terms of the role of temporal relationships between stimuli in conditioning across the life span.     

Feedback and stimulus-offset timing effects in perceptual category learning

We examined how feedback delay and stimulus offset timing affected declarative, rule-based and procedural, information–integration category-learning. We predicted that small feedback delays of several hundred milliseconds would lead to the best information–integration learning based on a highly regarded neurobiological model of learning in the striatum. In Experiment 1 information–integration learning was best with feedback delays of 500 ms compared to delays of 0 and 1000 ms. This effect was only obtained if the stimulus offset following the response. Rule-based learning was unaffected by the length of feedback delay, but was better when the stimulus was present throughout feedback than when it offset following the response. In Experiment 2 we found that a large variance (SD = 150 ms) in feedback delay times around a mean delay of 500 ms attenuated information–integration learning, but a small variance (SD = 75 ms) did not. In Experiment 3 we found that the delay between stimulus offset and feedback is more critical to information–integration learning than the delay between the response and feedback. These results demonstrate the importance of feedback timing in category-learning situations where a declarative, verbalizable rule cannot easily be used as a heuristic to classify members into their correct category.     

Does a sensory processing deficit explain counting accuracy on rapid visual sequencing tasks in adults with and without dyslexia?

The experiments conducted aimed to investigate whether reduced accuracy when counting stimuli presented in rapid temporal sequence in adults with dyslexia could be explained by a sensory processing deficit, a general slowing in processing speed or difficulties shifting attention between stimuli. To achieve these aims, the influence of the inter-stimulus interval (ISI), stimulus duration, and sequence length were evaluated in two experiments. In the first that used skilled readers only, significantly more errors were found with presentation of long sequences when the ISI or stimulus durations were short. Experiment 2 used a wider range of ISIs and stimulus durations. Compared to skilled readers, a group with dyslexia had reduced accuracy on two-stimulus sequences when the ISI was short, but not when the ISI was long. Although reduced accuracy was found on all short and long sequences by the group with dyslexia, when performance on two-stimulus sequences was used as an index of sensory processing efficiency and controlled, group differences were found with presentation of stimuli of short duration only. We concluded that continuous, repetitive stimulation to the same visual area can produce a capacity limitation on rapid counting tasks in all readers when the ISIs or stimulus durations are short. While reduced accuracy on rapid sequential counting tasks can be explained by a sensory processing deficit when the stimulus duration is long, slower processing speed in the group with dyslexia explains the greater inaccuracy found as sequence length is increased when the stimulus duration is short.     

Timing in trace conditioning of the nictitating membrane response of the rabbit (Oryctolagus cuniculus): scalar, nonscalar, and adaptive features

Using interstimulus intervals (ISIs) of 125, 250, and 500 msec in trace conditioning of the rabbit nictitating membrane response, the offset times and durations of conditioned responses (CRs) were collected along with onset and peak latencies. All measures were proportional to the ISI, but only onset and peak latencies conformed to the criterion for scalar timing. Regarding the CR's possible protective overlap of the unconditioned stimulus (US), CR duration increased with ISI, while the peak's alignment with the US declined. Implications for models of timing and CR adaptiveness are discussed.     

Visual discrimination of vowel duration

Discrimination of vowel duration was explored with regard to discrimination threshold, error bias, and effects of modality and consonant context. A total of 122 normal-hearing participants were presented with disyllabic-like items such as /lal-lal/ or /mam-mam/ in which the lengths of the vowels were systematically varied and were asked to judge whether the first or second vowel was longer. Presentation was either visual, auditory, or audiovisual. Vowel duration differences varied in 24 steps: 12 with a longer first /a/ and 12 with a longer last /a/ (range: ±33–400 ms). Results: 50% JNDs were smaller than the lowest tested step size (33 ms); 75% JNDs were in the 33–66 ms range for all conditions but V /lal/, with a 75% JND at 66–100 ms. Errors were greatest for visual presentation and for /lal-lal/ tokens. There was an error bias towards reporting the first vowel as longer, and this was strongest for /mam-mam/ and when both vowels were short, possibly reflecting a sublinguistic processing strategy.     

时距的短时保持: 缩短还是变长

采用Wearden和Ferrara(1993)的经典方法, 分别考察了1s以下(350 ms~650 ms)和1s以上(1000 ms ~ 2000 ms)不同类型(空、实时距)和通道(视、听)时距的短时保持效应。实验1发现, 不同刺激通道条件下, 1s以下时距的短时保持都呈现出主观缩短, 其中视觉条件比听觉条件明显; 实验2表明, 1s以上时距在不同刺激通道条件下都呈现出主观变长, 其中听觉条件比视觉条件明显。分析表明, 主观缩短趋势可能是由主观缩短效应和正的顺序误差效应共同作用所致, 而主观变长趋势是由主观变长效应和负的顺序误差效应造成的。     

Intramodal and crossmodal pairing and anchoring in comparisons of successive stimuli

Two experiments were conducted to study effects of modality, temporal position, and their interaction on comparisons of successive stimuli. In Experiment 1, intramodal (tone–tone and line–line) and crossmodal (tone–line and line–tone) stimulus pairs, with two interstimulus intervals (ISIs), 400 and 2,000 ms, were presented. Participants indicated which stimulus was the “stronger.” Time-order errors (TOEs) were assessed using the D% measure and were found in all types of pairs. Variation in TOEs across conditions was well accounted for by changes in parameters (stimulus weights, reference levels) in an extended version of Hellström’s sensation weighting (SW) model. With an ISI of 2,000 ms, the first stimulus had a lower weight (less impact on the response) than did the second stimulus. More negative TOEs were found with the longer ISI in all pair types except tone–line. In Experiment 2, participants indicated which of two lines was the longer or which of two tones was the louder. An intra- or crossmodal anchor, or no anchor, was interpolated between the stimuli. Anchoring tended to reduce the weight of the first stimulus, suggesting interference with memory, and to yield negative TOEs. Intramodal anchors yielded reduced weights of both stimuli, most dramatically for tones, suggesting an additional effect of stimulus interference. Response times decreased with crossmodal anchors. For line–line pairs, strong negative TOEs were found. In both experiments, the variation in TOE across conditions was well accounted for by the SW model.     

元音范畴知觉中特征分析和整合的时间进程

采用启动范式,在三个实验中通过操纵启动音和目标音的频谱相似度和时间间隔,考察了汉语听者元音范畴知觉中特征分析和整合的时间进程。结果发现随着启动音（从纯音、复合音到目标元音本身）和目标元音频谱相似度的增加,启动效应延续的时间越来越长。实验结果支持语音范畴知觉存在早期的声学特征分析和整合到后期的范畴知觉阶段,并为这些加工阶段的时间进程提供了初步的证据。     

Nonselective read-out from iconic memory in normal, borderline and retarded adolescents

The hypothesis that retarded individuals read-out information from iconic memory at a slower rate, relative to their CA matched peers, was tested. Three IQ groups (normal, borderline and retarded) were selected with 10 subjects in each group. A tachistoscope presented a stimulus array and a post-stimulus cue for 100 msec. each, separated by a variable interstimulus interval (ISI). This stimulus array consisted of 10 letters arranged on two horizontal rows. The post-stimulus cue was a circle which surrounded the position of the correct letter. Nine ISIs were used and ranged from −100 (cue before array) to 500 msec. A 3 × 9 repeated-measures analysis of variance revealed non-significant effects for IQ and the IQ × ISI interaction. A significant effect was found for ISIs (p < .01) which reflected reduced performance at the intermediate ISIs for all intelligence groups. The hypothesis of a read-out deficit in the retarded was not supported. The present findings were discussed in relation to previous research which supported a read-out deficit in the retarded.     

Inhibitory mechanisms in single negative priming from ignored and briefly flashed primes: The key role of the inter-stimulus interval

The influence of interstimulus intervals (ISIs) on priming effects was investigated using a single-prime negative priming (NP) paradigm. In all experiments, a brief (16 ms), centrally displayed prime (a Chinese character, to be ignored) appeared, followed by a pattern mask and then a centrally displayed target (another semantically related or unrelated Chinese character); the task required semantic categorization (animate/inanimate) of the target. An ISI could occur either between prime and mask (Experiments 1 and 5) or between mask and target (Experiments 2–4). The results revealed NP when a 470 ms ISI occurred between prime and mask (Experiments 1 and 5) and when a 700 ms ISI occurred between mask and target (Experiments 3 and 4). In contrast, when a long prime-target SOA was maintained but the mask-target ISI was shortened, NP disappeared (Experiment 4). The results indicated that a persisting mask/distractor (without ISI) located in the same position as the following target interfered with the buildup of inhibition, but an ISI between prime and mask or mask and target eliminated this interference, and that inhibition processes induced by an ignore instruction were implemented faster with an ISI placed between prime and mask than with an ISI placed between mask and target.