Color discrimination on Mangaia

Bornstein’s hypothesis that there is a loss of color discrimination in tropical areas was not supported in earlier research in the Cook Islands. Using a more sensitive color vision test (the Farnsworth-Munsell 100-Hue Test), a loss of color discrimination in the red-purple and blue-green regions of the spectrum was found. The lack of sex differences in this color discrimination loss supports a physiological rather than a genetic explanation of the observed decrement.     

Color discrimination and luminance

This experiment studied the relation between luminance level and color discrimination at 570 millimicrons. A variety ofstimuli whose luminances varied from .1 to 100 ft-L were viewed against a variety of surrounds. 1t was found that color discrimination ability was a joint function of the luminance level of the stimulus and the ratio of the luminance of the stimulus to that of the surround.     

Color is necessary for face discrimination in the Northern paper wasp,Polistes fuscatus

Animal Cognition - Visual individual recognition requires animals to distinguish among conspecifics based on appearance. Though visual individual recognition has been reported in a range of taxa...     

Nestling recognition via direct cues by parental male bluegill sunfish (<Emphasis Type="Italic">Lepomis macrochirus</Emphasis>)

Parental care can be costly to a parent in terms of both time and energy invested in the young. In species with cuckoldry or brood parasitism not all of the young under a parent's care are necessarily offspring. In such cases, distinguishing between kin and non-kin, and investing only in the former (nepotism), can be advantageous. Bluegill sunfish (Lepomis macrochirus) are characterized by paternal care and cuckoldry, and care-providing males appear to show nepotistic behaviours. Here, we investigated nestling recognition in bluegill, determining whether parental males can differentiate between young from their own nest (familiar and related) and young from non-neighbouring nests (unfamiliar and unrelated) using (1) visual and chemical cues, and (2) chemical cues only. In the first experiment, wild-caught parental males were presented with samples of eggs or fry (newly hatched eggs) collected from their own nest or a foreign nest and placed on opposite sides of an aquarium. The time these parental males spent associating with each sample, and their "pecking" behaviours (indicating cannibalism), were recorded. Parental males showed no preference between eggs from their own nest and eggs from a non-neighbouring nest, but they preferred to associate with fry from their own nest over foreign fry. There also was a positive relationship between male body size and the time spent associated with fry from their own nest. Parental males pecked at foreign fry more than 5 times as often as fry from their own nest, though this difference was not statistically significant. In the second experiment, fry that were collected from the nest of a wild-caught parental male or a non-neighbouring nest were placed in different containers and the water from each was dripped into opposite ends of an aquarium. The time the male spent on each side was recorded. In this case, parental males spent more time near the source of water conditioned by unrelated fry, but there was a positive relationship between male condition (fat reserves) and the time he spent near the source of water conditioned by fry from his own nest. Results confirm that chemicals cue nestling recognition by parental male bluegill. Electronic Publication     

Color discrimination under chronic hypoxic conditions (simulated climb "Everest-Comex 97")

Hypoxia is known to alter visual functions. In the present study, the effects of chronic hypobaric hypoxia upon visual color discrimination were studied in 8 subjects participating in a simulated climb from sea level (PO2 = 210 hPa) to 8,848 m (PO2 = 70 hPa) over a 31-day period of confinement in a decompression chamber ('Everst-Comex 97'). During these investigations, the subjects were required to discriminate between colors of different hue in the red, blue, and green ranges. Alterations in color discrimination increased slightly but significantly as altitude increased. Impairments occurred mainly in the red and blue ranges. In addition, our results further indicate that color discrimination would be affected only when a minimum threshold of difference between color stimuli is not present. Methodological and physiological implications are discussed.     

Visual discrimination in the toad

Using a method of successive discrimination, 10 toads (Bufo bufo), were trained to discriminate between horizontal and vertical rectangles each 5.0 ± 7.5 cm. After training, one optic nerve was severed in certain animals and the stumps pushed well apart to delay regeneration. The non-operated animals retained their learning over the rest-period of 10 weeks at a level similar to training. The animals with one eye showed considerably less retention than the non-operated animals.     

Conditional discrimination learning in the pigeon

Four pigeons received conditional discrimination training in which reinforcement contingencies were related to specific combinations of color and form, but were unrelated to either color or form considered separately. During discrete-trial training, each response in the presence of two of four color-form displays produced reinforcement and terminated the trial; responding to the other two displays was never reinforced, and each such response prolonged the particular trial on which it occurred. Subsequently, the subjects received multiple-schedule training in which responding to either of the displays previously associated with reinforcement was now reinforced on a variable-interval schedule, and extinction was the schedule again correlated with the other two displays. After differential responding to the stimuli was clearly evident, intensity of the combination displays was changed in subsequent training sessions. Complex stimulus control was generally maintained across variation in intensity, although there were temporary disruptions in performance associated with onset of some of the intensity changes. Finally, a component-stimulus test revealed considerably more responding to the forms than to the colors.     

Temporal discrimination in the split brain

Divided visual field studies of neurologically normal adults indicate that the left hemisphere is superior to the right in making temporal judgments. Some neuroimaging and neuropsychological studies, however, have suggested a role for the right hemisphere in temporal processing. We tested the divided hemispheres of a split-brain patient in two tasks requiring temporal judgments about visually presented stimuli. In one task, the patient judged whether two circles presented to one visual field appeared for the same or different durations. In the second task, the patient judged whether the temporal gaps in two circles occurred simultaneously or sequentially. In both tasks, the performance of the right hemisphere was superior to that of the left. This suggests that the right hemisphere plays an important role in making temporal judgments about visually presented stimuli.     

Color and intensity discrimination in <Emphasis Type="Italic">Xenopus laevis</Emphasis> tadpoles

Investigations into the physiology of Xenopus laevis have the potential to greatly accelerate biomedical research, especially concerning neural plasticity and sensory systems, but are limited by the lack of available information on behavioral learning in this species. Here, we attempt to lay the foundations for a behavioral assay in Xenopus that can be used in conjunction with biological manipulations. We tested cohorts of Xenopus tadpoles across four light-mediated active-avoidance experiments, using either wavelength or intensity as the salient discriminative cue. In the wavelength task, we determine a baseline learning rate and characterize retention of learning, identifying active extinction effects as far more potent than the passage of time in the loss of behavior. In the intensity task, we examine the effects of varying differences between the discriminative stimuli on acquisition and extinction and identify a critical range of intensity differences where learning changes. The results of our experiments demonstrate that Xenopus is a tractable model organism for cognitive research and can learn a variety of associative tasks in the laboratory settings. These data reveal new aspects of the Xenopus larval visual processing system and facilitate future research between cognitive methods and biological/chemical manipulations to study mechanisms of brain structure and function.     

Direct transfer from a horizontal-vertical discrimination to a brightness discrimination in the rat

Eight rats were trained on a discrimination between horizontal and vertical striations, and subsequently between black and white vertical striations. Subjects originally trained with horizontal positive preferred black to white and subjects trained with vertical positive preferred white to black.

The present note reports briefly on a transfer effect in rats, observed incidentally in an experiment designed for a different purpose. The rats were trained in a jumping stand to discriminate between horizontal and vertical striations, and when training was complete, were tested on a brightness discrimination.     

Temporal discrimination increases in precision over development and parallels the development of numerosity discrimination

Time perception is important for many aspects of human behavior, and a large literature documents that adults represent intervals and that their ability to discriminate temporal intervals is ratio dependent. Here we replicate a recent study by vanMarle and Wynn (2006) that used the visual habituation paradigm and demonstrated that temporal discrimination in 6-month-old infants is also ratio dependent. We further demonstrate that between 6 and 10 months of age temporal discrimination increases in precision such that by 10 months of age infants succeed at discriminating a 2:3 ratio, a ratio that 6-month-old infants were unable to discriminate. We discuss the potential implications of the fact that temporal discrimination follows the same developmental progression that has been previously observed for number discrimination in infancy (Lipton & Spelke, 2003).