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Consistency in women's orientations to food and nutrition in midlife and older age: a 10-year qualitative follow-up.

OBJECTIVE: The objective of this study was to discover and understand women's perceptions of stability and change in their orientations to food and nutrition during a time of physical, social, and psychological transitions. DESIGN: A 10-year follow-up to a 1988 study was conducted. PARTICPANTS/SETTINGS: Seventeen women from a 1988 study in a semirural county in New York participated. They were well-educated, Caucasian mothers, aged 44 to 75 years in 1998. METHODS: Semistructured, qualitative interviews in 1988 and 1998 were analyzed using grounded theory analysis. The 1998 and 1988 interviews with the same women were compared to understand patterns in orientations to food and nutrition. The life-course perspective was a conceptual guide. RESULTS: Most women in this sample described consistent orientations to food and nutrition at interviews 10 years apart. Even in the face of expected and unexpected changes in healthy, social environment, and roles, 14 of the 17 women perceived that their thoughts, beliefs, and strategies related to food and nutrition had been consistent across 10 years. The few women who perceived that they had changed orientations attributed changes to debilitating disease and transitions in work and family roles. IMPLICATIONS: Perceptions of consistency in their orientations to food and nutrition through midlife and older age among these women may be signs of stable trajectories that influence their response to nutrition education and their approach to dietary change.

Adult↗

Excitation and inhibition in orientation selectivity of cat visual cortex neurons revealed by whole-cell recordings in vivo.

One striking transformation in response properties that occurs in the geniculo-cortical pathway is the appearance of a high degree of orientation selectivity in the cortex. This property may be conceived as arising purely from the excitatory inputs to the cell, as being structured largely by the inhibition a cortical cell receives or could be due to a combination of the two. We have studied the contributions of excitatory and inhibitory inputs to cortical cells' orientation selectivity by analyzing the postsynaptic potentials evoked in cat striate neurones by flashing stimuli of different orientations. We made these recordings using the in vivo whole-cell technique (Xing Pei et al., 1991), which provides more stable and reliable results than classical intracellular recording methods. Our results show that the cat striate cortex exhibits a variety of mechanisms to achieve orientation selectivity. Orientation selectivity of a particular cell can be created by excitatory, by inhibitory, or by a combination of both mechanisms.

Animals↗

Is Posner's "beam" the same as Treisman's "glue"?: On the relation between visual orienting and feature integration theory.

In the present study we investigated whether the visually allocated "beam" studied by Posner and others is the same visual attentional resource that performs the role of feature integration in Treisman's model. Subjects were cued to attend to a certain spatial location by a visual cue, and performance at expected and unexpected stimulus locations was compared. Subjects searched for a target letter (R) with distractor letters that either could give rise to illusory conjunctions (PQ) or could not (PB). Results from three separate experiments showed that orienting attention in response to central cues (endogenous orienting) showed similar effects for both conjunction and feature search. However, when attention was oriented with peripheral visual cues (exogenous orienting), conjunction search showed larger effects of attention than did feature search. It is suggested that the attentional systems that are oriented in response to central and peripheral cues may not be the same and that only the latter performs a role in feature integration. Possibilities for future research are discussed.

Attention↗

Spatial layout, orientation relative to the observer, and perceived projection in pictures viewed at an angle.

Judgments of the spatial layout of a three-dimensional array of pictured dowels remain relatively constant as viewing angle changes, whereas judgments of their orientation relative to the observer (perceived orientation) vary. These changes in perceived orientation as viewing angle changes, called the differential rotation effect (DRE), also occur for stimuli such as the eyes in portraits, which are not extended in pictorial space. Thus, the mechanism for the DRE does not depend on the extension of pictured objects in depth. The DRE is decreased when back-illuminated pictures are viewed in the dark so that the picture plane is not visible. This result suggests that the DRE depends on information that defines a pictured object's direction relative to the picture plane. The difference in the way spatial layout and perceived orientation are affected by changes in viewing angle suggests that it is important to distinguish between these two attributes of pictures. In addition, another attribute, the picture's projection, should be distinguished from spatial layout and perceived orientation. When these distinctions are not made, the result is confusion, particularly when discussing whether or not pictures viewed at an angle appear distorted.

Attention↗

Reflexive and voluntary orienting of visual attention: time course of activation and resistance to interruption.

To study the mechanisms underlying covert orienting of attention in visual space, subjects were given advance cues indicating the probable locations of targets that they had to discriminate and localize. Direct peripheral cues (brightening of one of four boxes in peripheral vision) and symbolic central cues (an arrow at the fixation point indicating a probable peripheral box) were compared. Peripheral and central cues are believed to activate different reflexive and voluntary modes of orienting (Jonides, 1981; Posner, 1980). Experiment 1 showed that the time courses of facilitation and inhibition from peripheral and central cues were characteristic and different. Experiment 2 showed that voluntary orienting in response to symbolic central cues is interrupted by reflexive orienting to random peripheral flashes. Experiment 3 showed that irrelevant peripheral flashes also compete with relevant peripheral cues. The amount of interference varied systematically with the interval between the onset of the relevant cue and of the distracting flash (cue-flash onset asynchrony) and with the cuing condition. Taken together, these effects support a model for spatial attention with distinct but interacting reflexive and voluntary orienting mechanisms.

Adult↗

Orienting attention without awareness.

Previous research has shown that visual attention can be directed to a spatial location in 2 qualitatively different ways. Attention can be allocated endogenously in response to centrally presented precues, or it can be captured exogenously by a visual stimulus with an abrupt onset. It has been suggested that exogenous orienting of attention is an automatic process, whereas endogenous orienting of attention represents a controlled and strategic process. M.I. Posner and C.R.R. Snyder (1975) suggested that an automatic process occurs without intention, does not interfere with other mental processes, and does not necessarily give rise to awareness, whereas a controlled process will likely interfere with other processes and necessarily requires intention and awareness. Three experiments investigated the role of awareness in orienting visual attention. Endogenous and exogenous components of orienting attention were placed in opposition to each other to assess the automaticity of exogenous orienting by examining the potential for brief stimulus events to capture attention in the absence of subjective awareness. Results show that an exogenous cue presented below a subjective threshold of awareness captured attention automatically and without awareness.

Attention↗

Seeing and hearing rotated faces: influences of facial orientation on visual and audiovisual speech recognition.

It is well-known that facial orientation affects the processing of static facial information, but similar effects on the processing of visual speech have yet to be explored fully. Three experiments are reported in which the effects of facial orientation on visual speech processing were examined using a talking face presented at 8 orientations through 360 degrees. Auditory and visual forms of the syllables /ba/, /bi/, /ga/, /gi/, /ma/, /mi/, /ta/, and /ti/ were used to produce the following speech stimulus types: auditory, visual, congruent audiovisual, and incongruent audiovisual. Facial orientation did not affect identification of visual speed per se or the near-perfect accuracy of auditory speech report with congruent audiovisual speech stimuli. However, facial orientation did affect the accuracy of auditory speech report with incongruent audiovisual speech stimuli. Moreover, the nature of this effect depended on the type of incongruent visual speech used. Implications for the processing of visual and audiovisual speech are discussed.

Acoustic Stimulation↗

The effect on form perception of change of orientation in the third dimension.

The experiments reported here concern the effect of change of orientation of figures in the third dimension on phenomenal shape. In one experiment, novel two-dimensional wire figures were first shown in one orientation in the sagittal plane, and recognition of them was then tested in an altered orientation in that plane. In another experiment, novel three-dimensional wire figures were first shown in one orientation, and recognition of them was tested following rotation about one of the three major axes of space. The guiding hypotheses were (a) form perception is the end result of a process of figural description; (b) orientation change that alters the perceived location of the top, bottom, and sides of a figure will affect this description; and (c) front-back reversal and rotations about the Y axis will not affect the description because front and back constitute the sides of a figure much as left and right do, and all figural sides are phenomenally equivalent. The findings support these hypotheses except for an unanticipated effect on recognition of 90 degrees rotations about the Y axis. This effect was seen as a hitherto unknown example of egocentrism in perception, since the description is governed by the retinal projection resulting from the particular vantage point of the observer.

Depth Perception↗

Orientation specificity and spatial updating of memories for layouts.

This article examines the degree to which knowledge about the body's orientation affects transformations in spatial memory and whether memories are accessed with a preferred orientation. Participants learned large paths from a single viewpoint and were later asked to make judgments of relative directions from imagined positions on the path. Experiments 1 and 2 contribute to the emerging consensus that memories for large layouts are orientation specific, suggesting that prior findings to the contrary may not have fully accounted for latencies. Experiments 2 and 3 show that knowledge of one's orientation can create a preferred direction in spatial memory that is different from the learned orientation. Results further suggest that spatial updating may not be as automatic as previously thought.

Adult↗

Dopamine in the lateral caudate-putamen of the rat is essential for somatosensory orientation.

The present study examined the possible localization of somatosensory orientation in the caudate-putamen (CP) of the rat. In the first experiment, 6-hydroxydopamine (6-OHDA) was injected into either the anterodorsal (AD), anteroventral (AV), posterodorsal (PD), or posteroventral (PV) CP. Only rats with PV-CP 6-OHDA injections showed impaired orientation scores. However, these PV injections often caused widespread CP dopamine (DA) depletions, and no specific CP region appeared to be particularly associated with somatosensory orientation. In the second experiment, multiple injections of 6-OHDA were directed toward the medial or lateral halves of the CP to assess their relative contributions directly. DA depletions confined to the lateral (but not medial) CP resulted in orientation deficits; these deficits were greater than would be predicted from the volume of CP/DA loss. Furthermore, the magnitude of the DA fluorescence loss in the lateral CP was more highly correlated with the orientation impairment than was the medial CP fluorescence loss. Thus the lateral CP contributes to sensorimotor functions to a greater extent than does the medial CP, but the volume of CP/DA depletion also appears important.

Animals↗

Effect of visual experience on the habituation of orienting behavior.

Orienting behavior elicited by novel visual and auditory stimuli was examined in light-reared (LR) and dark-reared (DR) rats at 30, 60, 90, or 120 days of age. Orienting behavior was assessed by examining the rat's ability to interrupt ongoing licking and perform appropriate head and postural adjustments when apparently moving or stationary light displays or tones were presented. When the lights were first presented to the LR and DR rats, their orienting behavior did not differ at any of the ages examined. However, age and visual experience did influence habituation and recovery of orienting with changes in the light display. The older DR rats habituated with fewer repeated presentations of the light displays than their LR counterparts and did not recover orienting as effectively to all the subsequent changes of the light displays. The younger LR and DR rats did not differ reliably. These results are discussed with regard to the nature of the habituation process for rodents and the relation between visual experience and habituation of attentional responses.

Animals↗

Discrimination of shape reflections and shape orientations by Columba livia.

By using a free-operant instrumental discrimination procedure, it was demonstrated that pigeons find two-dimensional mirror-image visual forms more difficult to distinguish than otherwise similar forms. Variations in orientation of the discriminanda exacerbated the relative confusability of mirror images. No significant difference was found in the pigeons' performance whether the birds were discriminating vertically or horizontally reflected mirror-image pairs. Mirror images of shapes were also shown to be less discriminable than upside-down versions of shapes. The similarity of mirror-image patterns is discussed in relation to the generalized recognition of bilaterally symmetrical forms by pigeons. Pigeons found an orientation discrimination task involving a 45 degree tilt comparatively hard. A second experiment with a discrete-trial conditional paradigm confirmed that discriminations of shape orientations can be difficult for these birds. The addition of shape cues improved the performance on the orientation discrimination task, more so when arbitrary shapes were employed than when mirror images were used, which indicates again that the latter were more difficult to discriminate than the former. The relative insensitivity to shape orientations is ascribed to normal ecological demands on pigeons.

Animals↗

Ontogeny of orientation flight in the honeybee revealed by harmonic radar.

Cognitive ethology focuses on the study of animals under natural conditions to reveal ecologically adapted modes of learning. But biologists can more easily study what an animal learns than how it learns. For example, honeybees take repeated 'orientation' flights before becoming foragers at about three weeks of age. These flights are a prerequisite for successful homing. Little is known about these flights because orienting bees rapidly fly out of the range of human observation. Using harmonic radar, we show for the first time a striking ontogeny to honeybee orientation flights. With increased experience, bees hold trip duration constant but fly faster, so later trips cover a larger area than earlier trips. In addition, each flight is typically restricted to a narrow sector around the hive. Orientation flights provide honeybees with repeated opportunities to view the hive and landscape features from different viewpoints, suggesting that bees learn the local landscape in a progressive fashion. We also show that these changes in orientation flight are related to the number of previous flights taken instead of chronological age, suggesting a learning process adapted to changes in weather conditions, flower availability and the needs of bee colonies.

Animal Communication↗

Orientation-selective adaptation and tilt after-effect from invisible patterns.

Exposure to visual patterns of high contrast (for example, gratings formed by alternating white and black bars) creates after-effects in perception. We become temporarily insensitive to faint test patterns that resemble the pre-exposed pattern (such as gratings of the same orientation), and we require more contrast to detect them. Moreover, if the test pattern is slightly tilted relative to the pre-exposed one, this tilt may be perceptually exaggerated: we experience a tilt after-effect. Here we show that these visual after-effects occur even if the pre-exposed grating is too fine to be perceptually resolved. After looking at a very fine grating, so high in spatial frequency that it was perceptually indistinguishable from a uniform field, observers required more contrast to detect a test grating presented at the same orientation than one presented at the orthogonal orientation. They also experienced a tilt after-effect that depended on the relation of the test pattern's tilt to the unseen orientation of the pre-exposed pattern. Because these after-effects are due to changes in orientation-sensitive mechanisms in visual cortex, our observations imply that extremely fine details, even those too fine to be seen, can penetrate the visual system as far as the cortex, where they are represented neurally without conscious awareness.

Adaptation, Physiological↗

The contribution of sensory experience to the maturation of orientation selectivity in ferret visual cortex.

Sensory experience begins when neural circuits in the cerebral cortex are still immature; however, the contribution of experience to cortical maturation remains unclear. In the visual cortex, the selectivity of neurons for oriented stimuli at the time of eye opening is poor and increases dramatically after the onset of visual experience. Here we investigate whether visual experience has a significant role in the maturation of orientation selectivity and underlying cortical circuits using two forms of deprivation: dark rearing, which completely eliminates experience, and binocular lid suture, which alters the pattern of sensory driven activity. Orientation maps were present in dark-reared ferrets, but fully mature levels of tuning were never attained. In contrast, only rudimentary levels of orientation selectivity were observed in lid-sutured ferrets. Despite these differences, horizontal connections in both groups were less extensive and less clustered than normal, suggesting that long-range cortical processing is not essential for the expression of orientation selectivity, but may be needed for the full maturation of tuning. Thus, experience is beneficial or highly detrimental to cortical maturation, depending on the pattern of sensory driven activity.

Animals↗

Predicting the orientation of invisible stimuli from activity in human primary visual cortex.

Humans can experience aftereffects from oriented stimuli that are not consciously perceived, suggesting that such stimuli receive cortical processing. Determining the physiological substrate of such effects has proven elusive owing to the low spatial resolution of conventional human neuroimaging techniques compared to the size of orientation columns in visual cortex. Here we show that even at conventional resolutions it is possible to use fMRI to obtain a direct measure of orientation-selective processing in V1. We found that many parts of V1 show subtle but reproducible biases to oriented stimuli, and that we could accumulate this information across the whole of V1 using multivariate pattern recognition. Using this information, we could then successfully predict which one of two oriented stimuli a participant was viewing, even when masking rendered that stimulus invisible. Our findings show that conventional fMRI can be used to reveal feature-selective processing in human cortex, even for invisible stimuli.

Adult↗

Three-dimensional orientation tuning in macaque area V4.

Tuning for the orientation of elongated, linear image elements (edges, bars, gratings), first discovered by Hubel and Wiesel, is considered a key feature of visual processing in the brain. It has been studied extensively in two dimensions (2D) using frontoparallel stimuli, but in real life most lines, edges and contours are slanted with respect to the viewer. Here we report that neurons in macaque area V4, an intermediate stage in the ventral (object-related) pathway of visual cortex, were tuned for 3D orientation--that is,for specific slants as well as for 2D orientation. The tuning for 3D orientation was consistent across depth position (binocular disparity) and position within the 2D classical receptive field. The existence of 3D orientation signals in the ventral pathway suggests that the brain may use such information to interpret 3D shape.

Animals↗

Orienting attention in audition and between audition and vision: young and elderly subjects.

This study examined 30 young and 10 elderly subjects to test whether orienting of attention could be measured in audition. Orienting in a mixed-modal condition in which stimuli were either auditory or visual was also tested. The dependent measure was the reaction time (RT) to lateralized targets when the locations were predicted by antecedent arrow cues that were correct (valid), were incorrect (invalid), or provided no lateralizing information (neutral). A comparison between the two groups among the different conditions showed that elderly subjects had longer RTs than the younger participants, but the pattern of results was similar in both groups. In addition, a similar RT pattern was found for each modal condition: Valid trials elicited the fastest responses and invalid trials the slowest. These findings suggest that the mechanisms involved in orienting attention operate in audition and that individuals may allocate their processing resources among multiple sensory pools. Moreover, effects seen in orienting attention in audition were similar to those found in vision and are interpretable with the same types of models. Orienting attention appears to be relatively resistant to the aging process in the sample of subjects tested in this study.

Acoustic Stimulation↗