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J Wattam-Bell

Publications and source records attributed to J Wattam-Bell.

7 recordsLinked to original sources

The development of maximum displacement limits for discrimination of motion direction in infancy.

The development of visual motion mechanisms has been studied in infants by using forced-choice preferential looking to measure maximum displacement limits (dmax) for the detection of coherent motion in random-dot patterns. The motion consisted of a sequence of coherent displacements at intervals of 20 msec. Between 8 and 15 weeks, dmax for discrimination of coherent from incoherent motion, and for discrimination of opposite directions of coherent motion, increased with age; in both conditions, dmax for the oldest infants was less than a third of the value found in adults. For 10-11-week-old infants, and for an adult subject, reducing stimulus contrast from 88 to 48% had no effect on dmax for direction discrimination, which indicates that the rise in dmax with age is not simply a result of improving contrast sensitivity. When the displacement interval was increased from 20 to 40 msec, dmax increased significantly in 8-11-week-olds, but remained unchanged in 12-15-week-olds. These results show that while directional mechanisms are present in the visual system by 8 weeks, they operate over a restricted velocity range. The upper limit of this velocity range increases with age. After about 12 weeks, the increase is mainly due to changes in the spatial properties of motion mechanisms; however, in younger infants changes in their temporal properties are also important.

Adult

Orientation selectivity in infancy: behavioural evidence for temporal sensitivity.

One-month-old infants were tested with a habituation-recovery paradigm to determine whether they could discriminate phase-shifting grating patterns that switched between two orientations, three or eight times a second, from grating patterns that only shifted in phase. The infants were found to discriminate patterns switching orientation at the lower temporal rate of 3 reversals s-1, but not 8 reversals s-1. This finding supports the idea that orientation-selective mechanisms improve in their temporal sensitivity during early infancy. Where they can be compared, the results from behavioural and electrophysiological studies agree as to the course of this development.

Child

Changes in infants' ability to switch visual attention in the first three months of life.

The abilities of 1-month-old and 3-month-old infants to shift their gaze from a central target to a peripheral target were compared in four experiments. In experiment 1 targets matched in mean luminance to the background were presented to infants in the periphery at varying levels of contrast. The contrast thresholds for target detection were found to be significantly different for 1-month-olds compared with 3-month-olds. With targets set close to these contrast thresholds, correct refixations and the latency for shifting attention were examined in experiment 2. Two conditions were used: a peripheral target was presented against a homogeneous background (noncompetition); and in the second condition, the patterned target appeared at one of two lighter peripheral windows set against a darker background (competition). Although there was no difference between the two age groups in the latency for shifting visual attention, 1-month-olds were found to make more directional errors in the competition condition. The competition effect of two potential targets on latencies was examined in experiment 3. In the competition condition, two identical peripheral patterned targets were presented to the infants. The 3-month-olds refixated more quickly to one of the double targets in the competition condition than to a single peripheral target, whereas 1-month-olds were slowed down by a double target display. Finally, in experiment 4 the ability of the infants to process and disengage from a central stimulus and to refixate towards a similar peripheral target was examined. This type of competition disrupted both the direction of the first eye movement and the latency to shift attention in both age groups. However, the effect was significantly greater for the 1-month-olds. Taken together, the results of these experiments demonstrate the greater disruption of fixation-shift behaviour in 1-month-olds compared with 3-month-olds when competing visual stimuli are used. This developmental change is explained in terms of maturation of executive cortical orienting systems over the first months of life.

Age Factors

Development of motion-specific cortical responses in infancy.

The development of visual motion mechanisms has been studied in infants with a visual evoked potential (VEP) technique which isolates responses from directionally-selective mechanisms. In adults, the amplitude of this directional VEP increased with velocity up to a maximum at 15-20 deg/sec, and then declined with further increases in velocity. In a group of infants tested longitudinally, directional responses were first found at a median age of 74 days with a stimulus velocity of 5 deg/sec, and 90 days with a velocity of 20 deg/sec; this age difference was statistically significant. Initially, VEP amplitudes were significantly greater at 5 deg/sec than at 20 deg/sec. By the end of the longitudinal study, there was no significant difference in amplitudes at the two velocities. In a second group of infants, simultaneous recording of VEPs and electrooculograms indicated that eye movements tracking the stimulus were not a significant factor in the development of the directional VEP. It is concluded that the development of directional selectivity starts at low velocities, and extends to higher velocities with age.

Adult

Development of orientation discrimination in infancy.

It has previously been found by us, with a visual evoked potential (VEP) measure, that orientation discrimination of dynamic patterns in infants can be demonstrated from around 6 weeks after birth. Experiments are reported in which orientation discrimination was measured behaviourally, in two infant control habituation procedures, with both dynamic and static patterns. When dynamic patterns identical to those in our previous VEP studies were used, the first positive evidence of orientation discrimination was found at around 6 weeks postnatally. The time course of both the VEP and the behavioural measures was similar. However, with static patterns, evidence of orientation discrimination by newborns was found if the infants were allowed to compare the habituated and novel orientations in a paired simultaneous comparison after habituation, but was not found when the habituated and novel stimulus were presented sequentially. The positive evidence of orientation discrimination in newborns supports the hypothesis that some form of orientationally tuned detectors can be used for discrimination of static patterns at birth. However, some developmental change over several weeks seems to be required before a positive electrophysiological VEP response can be measured for dynamic patterns changing in orientation.

Child Development

Orientation-specific cortical responses develop in early infancy.

Neurones in the visual cortex of higher mammals differ from those elsewhere in the visual pathway in that the majority respond selectively to particular edge or bar orientations in the stimulus. We have developed a visually evoked potential (VEP) technique which isolates the response of orientation-selective mechanisms from that of cortical or sub-cortical neurones which lack orientation selectivity. We are unable to find such orientation-selective responses in newborn human infants within the sensitivity of our method, but repeated longitudinal testing of individual infants shows that measurable responses emerge around 6 weeks of age. This result is consistent with the idea that human cortical visual function is very immature at birth, but develops rapidly in the first two postnatal months.

Age Factors