Contents of Volume 58

Volume Contents

Contents of Volume 58     

Psychometric properties of the eating disorders inventory-2 among women seeking treatment for binge eating disorder

Psychometric properties of the Eating Disorders Inventory-2 (EDI-2) when used for women with Binge Eating Disorder (BED) are assessed. The EDI-2 was administered to 144 outpatients seeking treatment for BED and 152 outpatients seeking treatment for Bulimia Nervosa (BN). Most EDI-2 scales had acceptable internal consistence for both the BED and BN samples. EDI-2 scales demonstrated adequate stability within a subsample of those with BED who were retested. Confirmatory factor analyses revealed a hypothesized second-order two-factor structure for the original EDI scales for the BED group but not for those with BN. When the provisional EDI-2 scales were included, a two-factor structure was not supported for any group. Some scales differentiated the BED from the BN sample, and the second-order factors correlated with measures of similar constructs. The original EDI scales can be used reliably for those with BED.     

A presentation of Attentional Semantics

The paper presents the two main assumptions of Attentional Semantics—(A) and (B), and its main aim (C). (A) Conscious experience is determined by attention: there cannot be consciousness without attention. Consciousness is explained as the product of attentional activity. Attentional activity can be performed thanks to a special kind of energy: nervous energy. This energy is supplied by the organ of attention. When we perform attentional activity, we use our nervous energy. This activity directly affects the organ of attention, causing a variation in the state of the nervous energy. This variation constitutes the phenomenal aspect of consciousness. (B) Words are tools to pilot attention. The meanings of words isolate, de-contextualize, “freeze” and classify in an articulated system the ever-changing and multiform stream of our conscious experiences. Each meaning is composed of the sequence of invariable elements that, independently of any individual occurrence of a given conscious experience, are responsible for the production of any instance of that conscious experience. The elements composing the meanings of words are attentional operations: each word conveys the condensed instructions on the attentional operations one has to perform if one wants to consciously experience what is expressed through and by it. (C) Attentional Semantics aims at finding the attentional instruction conveyed by the meanings of words. To achieve this goal, it tries: (1) to identify the sequence of the elementary conscious experiences that invariably accompany, and are prompted by, the use of the word being analyzed; (2) to describe these conscious experiences in terms of the attentional operations that are responsible for their production; and (3) to identify the unconscious and non-conscious operations that, directly or indirectly, serve either as the support that makes it possible for the attentional operations to take place, be completed, and occur in a certain way, or as the necessary complement that makes it possible to execute and implement the activities determined and triggered by the conscious experiences. The origins of Attentional Semantics are also presented, and the methodological problems researchers encounter when analyzing meanings in attentional terms are discussed. Finally, a brief comparison with the other kinds of semantics is made.     

Motion and color processing in school-age children and adults: an ERP study

Stimuli designed to selectively elicit motion or color processing were used in a developmental event-related potential study with adults and children aged 6, 7 and 8. A positivity at posterior site INZ (P-INZ) was greater to motion stimuli only in adults. The P1 and N1 were larger to color stimuli in both adults and children, but earlier to motion stimuli only in adults. Finally, the P2 was larger to color stimuli in adults but larger to motion stimuli in children, and earlier to motion stimuli only in children. The findings across components indicate development from middle childhood to adulthood in aspects of both the motion and color processing systems indexed by this paradigm, but are consistent with an hypothesis of a more protracted time course of development for the motion as compared to the color processing system.     

Understanding the effects of task-specific practice in the brain: Insights from individual-differences analyses

We used functional magnetic resonance imaging to study practice effects in different mental imagery tasks. The study was designed to address three general questions: First, are the results of standard group-based analyses the same as those of a regression method in which brain activation changes over individual participants are used to predict task performance changes? With respect to the effects of practice, the answer was clear: Group-based analyses produced different results from regression-based individual-differences analyses. Second, are all brain areas that predict practice effects consistently activated across participants? Again, the answer was clear: Most areas that predicted the effects of practice on performance were not activated consistently over participants. Finally, does practice affect different areas in different ways for different people in different tasks? The answer was again clear: The areas that predicted changes in performance with practice varied for the different tasks, but this was more dramatically and clearly revealed by the individual-differences analyses. In short, individual-differences analyses provided insights into the relation between changes in brain activation and changes in accompanying performance, and these insights were not provided by standard group-based analyses.     

Survival with an asymmetrical brain: advantages and disadvantages of cerebral lateralization

Recent evidence in natural and semi-natural settings has revealed a variety of left-right perceptual asymmetries among vertebrates. These include preferential use of the left or right visual hemifield during activities such as searching for food, agonistic responses, or escape from predators in animals as different as fish, amphibians, reptiles, birds, and mammals. There are obvious disadvantages in showing such directional asymmetries because relevant stimuli may be located to the animal's left or right at random; there is no a priori association between the meaning of a stimulus (e.g., its being a predator or a food item) and its being located to the animal's left or right. Moreover, other organisms (e.g., predators) could exploit the predictability of behavior that arises from population-level lateral biases. It might be argued that lateralization of function enhances cognitive capacity and efficiency of the brain, thus counteracting the ecological disadvantages of lateral biases in behavior. However, such an increase in brain efficiency could be obtained by each individual being lateralized without any need to align the direction of the asymmetry in the majority of the individuals of the population. Here we argue that the alignment of the direction of behavioral asymmetries at the population level arises as an "evolutionarily stable strategy" under "social" pressures occurring when individually asymmetrical organisms must coordinate their behavior with the behavior of other asymmetrical organisms of the same or different species.     

Intermittent exposure to social defeat and open-field test in rats: acute and long-term effects on ECG,body temperature and physical activity

This study investigated the effects of exposure to an intermittent homotypic stressor on: (i) habituation of acute autonomic responsivity (i.e. cardiac sympathovagal balance and susceptibility to arrhythmias), and (ii) circadian rhythmicity of heart rate, body temperature, and physical activity. After implantation of a transmitter for the radiotelemetric recording of electrocardiogram (ECG), body temperature and physical activity, adult male rats (Rattus norvegicus, Wild Type Groningen strain) were repeatedly exposed (10 consecutive times, on alternate days) to either a social stressor (defeat by a con-specific, n = 15) or an open-field, control challenge (transfer to a new cage; n = 8). ECGs, body temperature and physical activity were continuously recorded in baseline, test and recovery periods (each lasting 15 min), at the 1st and 10th episodes of both defeat and open-field challenge. The circadian rhythms of heart rate, body temperature and physical activity were monitored before (5 days), during (16 days) and after (21 days) the intermittent stress protocol. This study indicates that there is no clear habituation of either acute cardiac autonomic responsivity (as estimated by means of time-domain indexes of heart rate variability) or arrhythmia occurrence to a brief, intermittent, homotypic challenge, regardless of the nature of the stressor (social or non-social). On the other hand, rats exposed to social challenge also failed to show adaptation of acute temperature and activity stress responsiveness, whereas rats facing open-field challenge developed habituation of activity and sensitization of temperature responses. Repeated social challenge produced remarkable reductions of the heart rate circadian rhythm amplitude (this effect being significantly greater than that produced by intermittent open-field), but only minor changes in the daily rhythms of body temperature and physical activity.     

Role of motor imitation in traversability of surfaces by walking infants.

The ecological approach by Gibson stressed the role of visual cues in toddlers' locomotor activities. In particular, a rigid surface offers more traversability "affordances" to walkers (13-16 mo. old) than a deformable surface. On the other hand, imitation plays a relevant role in human behaviors. In our study a group of 17 walking infants (12-19 mo.) were asked to choose between locomoting on a rigid versus a deformable surface after having seen an older child walking on the deformable surface. A control group of 19 infants were asked to do the same task without having seen a model. The task was repeated three times. No relevant differences appeared between the two groups as to the choice of surfaces: the rigid surface was preferred by both groups. Some slight differences in the behavior of the experimental group were seen as a result of observing the model. Clearly, however, social stimulus. such as the sight of an older child performing a specific task, does not overcome the affordances which induce infants not to walk on the deformable surface.     

At the root of the left–right asymmetries in spatial–numerical processing: From domestic chicks to human subjects

In this review, we discuss evidence showing that birds (Gallus gallus and Nucifraga columbiana) represent numerical magnitudes as being oriented from left to right. Subjects, trained to identify a target element (i.e. the 4th) in a series of sagittally oriented identical elements, when required to generalise on an identical series oriented spatially from left to right, correctly identified the target element “counting” from the left of the array. Moreover, chicks, when presented with sets of 5 vs. 10 or 6 vs. 9 imprinting objects, which were made to disappear one at a time behind one of two identical screens, spontaneously inspected the screen which occluded the larger set. Interestingly, chicks scored a higher percentage of correct choices when the larger of the two sets was on their right side. Similarities with the phenomenon of the spatially oriented (left to right) number line in humans are discussed. Animal models promise a fresh approach to the understanding of developmental mechanisms underlying the expression of knowledge, offering attractive arguments for doubting the uniqueness of human numerical cognition.