The distinctiveness of hardiness, positive emotionality, and negative emotionality in National Guard soldiers

Exploratory and confirmatory factor analyses were used to investigate the distinctiveness of hardiness (using the Short Hardiness Scale; Bartone, 1995) from the broader personality traits of negative emotionality and positive emotionality (NEM and PEM; assessed with items from the MMPI-2 PSY-5 scales); in a sample of 981 Army National Guard soldiers. Exploratory factor analyses demonstrated that hardiness items loaded on a separate factor from PEM and NEM items, and confirmatory factor analysis suggested that hardiness is not simply a sub-facet of either PEM or NEM. However, subsequent regression analyses found that hardiness did not predict symptoms of PTSD or depression beyond the effects of PEM and NEM among combat exposed soldiers.     

内隐序列学习不受注意负荷的影响:来自眼动的证据

利用眼动记录方法,采用内隐序列学习的观察范式,通过操纵注意负荷高和低,考察内隐序列学习是否需要注意参与。结果发现:(1)在高、低注意负荷条件下都出现了内隐序列学习效应;(2)高注意负荷条件下眼跳反应时长于低注意负荷条件下的;(3)高、低注意负荷序列内隐序列学习量差异不显著,表明内隐序列学习不受注意负荷影响。     

Neural correlates of feigned memory impairment are distinguishable from answering randomly and answering incorrectly: an fMRI and behavioral study

Previous functional magnetic resonance imaging (fMRI) studies have identified activation in the prefrontal-parietal-sub-cortical circuit during feigned memory impairment when comparing with truthful telling. Here, we used fMRI to determine whether neural activity can differentiate between answering correctly, answering randomly, answering incorrectly, and feigned memory impairment. In this study, 12 healthy subjects underwent block-design fMRI while they performed digit task of forced-choice format under four conditions: answering correctly, answering randomly, answering incorrectly, and simulated feigned memory impairment. There were three main results. First, six areas, including the left prefrontal cortex, the left superior temporal lobe, the right postcentral gyrus, the right superior parietal cortex, the right superior occipital cortex, and the right putamen, were significantly modulated by condition type. Second, for some areas, including the right superior parietal cortex, the right postcentral gyrus, the right superior occipital cortex, and the right putamen, brain activity was significantly greater in feigned memory impairment than answering randomly. Third, for the areas including the left prefrontal cortex and the right putamen, brain activity was significantly greater in feigned memory impairment than answering incorrectly. In contrast, for the left superior temporal lobe, brain activity was significantly greater in answering incorrectly than feigned memory impairment. The results suggest that neural correlates of feigned memory impairment are distinguishable from answering randomly and answering incorrectly in healthy subjects.     

Generalized lessons about sequence learning from the study of the serial reaction time task

Over the last 20 years researchers have used the serial reaction time (SRT) task to investigate the nature of spatial sequence learning. They have used the task to identify the locus of spatial sequence learning, identify situations that enhance and those that impair learning, and identify the important cognitive processes that facilitate this type of learning. Although controversies remain, the SRT task has been integral in enhancing our understanding of implicit sequence learning. It is important, however, to ask what, if anything, the discoveries made using the SRT task tell us about implicit learning more generally. This review analyzes the state of the current spatial SRT sequence learning literature highlighting the stimulus-response rule hypothesis of sequence learning which we believe provides a unifying account of discrepant SRT data. It also challenges researchers to use the vast body of knowledge acquired with the SRT task to understand other implicit learning literatures too often ignored in the context of this particular task. This broad perspective will make it possible to identify congruences among data acquired using various different tasks that will allow us to generalize about the nature of implicit learning.     

Manipulating attentional load in sequence learning through random number generation

Implicit learning is often assumed to be an effortless process. However, some artificial grammar learning and sequence learning studies using dual tasks seem to suggest that attention is essential for implicit learning to occur. This discrepancy probably results from the specific type of secondary task that is used. Different secondary tasks may engage attentional resources differently and therefore may bias performance on the primary task in different ways. Here, we used a random number generation (RNG) task, which may allow for a closer monitoring of a participant's engagement in a secondary task than the popular secondary task in sequence learning studies: tone counting (TC). In the first two experiments, we investigated the interference associated with performing RNG concurrently with a serial reaction time (SRT) task. In a third experiment, we compared the effects of RNG and TC. In all three experiments, we directly evaluated participants' knowledge of the sequence with a subsequent sequence generation task. Sequence learning was consistently observed in all experiments, but was impaired under dual-task conditions. Most importantly, our data suggest that RNG is more demanding and impairs learning to a greater extent than TC. Nevertheless, we failed to observe effects of the secondary task in subsequent sequence generation. Our studies indicate that RNG is a promising task to explore the involvement of attention in the SRT task.     

Contrast as seen in visual search reaction times.

Three pigeons searched arrays of alphabetic letters displayed on computer monitors. On each trial, either an A or an E appeared, and the reaction time and accuracy with which the bird pecked at this target were measured. In each block of trials, each target (A or E) was displayed alone, or together with a number of distractor letters (2 or 18) that varied in their similarity to the target. During a baseline series of sessions, responses to the A and to the E each yielded food reinforcement on 10% of the trials. In the next series of sessions, reinforcement continued at 10% for A, but rose to 30% for E. In a final series, these reinforcement conditions were reversed. As expected, reaction times increased with target-distractor similarity and (for similar distractors) with the number of distractors. Increased reinforcement of E had no effect on reaction times to E, but produced a very consistent increase in reaction times to A; the average increase was constant across the various display conditions. Reversal of the differential reinforcement conditions reversed this contrast effect. Analysis of the reaction time distributions indicated that increased reinforcement to E decreased the momentary probability of response to A by a constant amount, regardless of display conditions. These results are discussed in relation to theories of contrast, memory, and of the search image.     

Shaping of rule-governed behaviour

Over an experimental session of 80 trials, subjects counted brief auditory stimuli ("clicks") in stimulus presentation periods and indicated the number counted by pressing a key the corresponding number of times in subsequent response periods. "Correct" answers resulted in feedback. Unknown to the subjects, the feedback criterion was based on speed of pressing rather than on the correct number of presses. Speed of pressing was modified by response consequences when feedback was made dependent on pressing faster or slower than baseline speed. Modification of speed occurred independently of rules and without the subjects' ability to describe contingency or response requirements. The results suggest that non-verbal contingencies may have a shaping effect on non-salient and non-described attributes of rule-governed behaviour, and it is argued that this may be an important control mechanism of low-level behavioural attributes that are unlikely to be guided by verbal discriminative stimuli.     

Rasch-representable reaction time distributions

This article investigates properties of a representation based on the Rasch test model for reaction times (RT) that was proposed by Micko. Necessary and sufficient conditions for a set of RT distributions to be Rasch-representable are derived. It is shown that independent serial and independent parallel processing models cannot be reconciled with the representation. However, random extreme models compatible with the Reasch-representation exist that assume RT is determined by the longest or he shortest processing time of a random number of independent paraloel channels. Nonparametric properties of Rasch-representable distributions are derived that can be used for testing the model and for estimating its parameters. Conditions are presented for Rasch-representable distributions to form a scale family. Finally, Rasch-represent-able distributions are characterized interms of their hazard functions.For helpful discussions, we are grateful to Hans Irtel, Christoph Micko, Hartmann Scheiblechner, and Hans-Henning Schultz.     

The role of verbal behavior in human learning: infant performance on fixed-interval schedules

The performances of two infants less than one year old were investigated on fixed-interval schedules. When the infants touched a cylinder either music or food was presented according to fixed-interval schedules ranging in value from 10 to 50 seconds. With respect to two principal criteria, namely, pattern of responding and sensitivity to the schedule parameter, the subjects' behavior closely resembled that of animals but differed markedly from that of older children and adults. Negatively accelerated responding in the course of the fixed interval in the early sessions gave way to a scalloped pattern, consisting of a pause after reinforcement followed by an accelerated response rate. This scalloped pattern was the final form of responding on all schedule values. Analysis of data after performance had stabilized showed that postreinforcement pause was a negatively accelerated increasing function, and running rate (calculated after excluding the postreinforcement pause) was a declining function, of schedule value. On each schedule, the durations of mean successive interresponse times declined in the course of the fixed interval and were directly related to schedule value. The results supported Lowe's (1979) suggestion that verbal behavior may be responsible for major differences in the schedule performance of older humans and animals.     

Burying by rats in response to aversive and nonaversive stimuli

Previous investigations have shown that rats bury a variety of conditioned and unconditioned aversive stimuli. Such burying has been considered as a species-typical defensive reaction. In the present studies, rats buried spouts filled with Tabasco sauce, or condensed milk to which a taste aversion was conditioned, but did not bury water-filled spouts or spouts filled with a palatable novel food (apple juice) to which a taste aversion was not conditioned. However, in other experiments rats consistently and repeatedly buried Purina Rat Chow, Purina Rat Chow coated with quinine, and glass marbles. This indicates that a variety of stimuli, not all aversive or novel, evoke burying by rats. Whereas the behavior may reasonably be considered as a species-typical defensive behavior in some situations, the wide range of conditions that occasion burying suggests that the behavior has no single biological function.