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Geisbauer, G., Griebel, U., Schmid, A., & Timney, B. (2004). Brightness discrimination and neutral point. Can. J. Zool, 82(4), 660–670.
Abstract: Abstract: Equine brightness discrimination ability and color discrimination were measured using a two-choice discrimination
task. Two Haflinger horses (Equus caballus L., 1758) were trained to discriminate 30 different shades of grey varying from low to high relative brightness. Their ability to distinguish shades of grey was poor, with calculated Weber fractions of 0.42 and 0.45. In addition, a “neutral point” test to determine the dimensionality of color vision was carried out. Three hues of blue-green were tested versus a range of grey targets with brightnesses similar to those of the blue-green targets. A neutral point was found at about 480 nm. Thus, we can conclude that horses possess dichromatic color vision. |
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Macuda, T., & Timney, B. (1999). Luminance and chromatic discrimination in the horse (Equus caballus). Behav. Process., 44(3), 301–307.
Abstract: Equine colour vision was measured under conditions that minimised the possibility of animals using brightness cues to make chromatic discriminations. In a two-stage study, we first obtained luminance discrimination functions for achromatic targets then tested for chromatic discrimination over a range of target luminances. Horses were trained on a two-choice discrimination task. The positive stimulus was varied in luminance and/or colour using neutral density and broad band colour filters. The negative stimulus appeared as a uniform grey. In the brightness discrimination task, the horses performed well at large luminance differences but their percentage of correct responses declined to near chance levels at differences of less than 0.2 log units. In addition, a decrement in performance was noted at luminance differences of less than 0.2 log units for green and yellow chromatic discrimination functions, suggesting that horses cannot easily discriminate yellow and green from grey. However, the chromatic discrimination functions for red and blue showed that animals performed very well across the full range of target luminances. These results suggest that horses are at least dichromats.
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Timney, B. (2008). Photopic Spectral Sensitivity and Wavelength Discrimination in the Horse (Equus caballus). In IESM 2008.
Abstract: A number of studies have demonstrated that horses have chromatic vision and are able to distinguish colours from grey, independent of brightness. Anatomical and physiological data support the view that they are dichromats. In two experiments we provide behavioural evidence for their dichromacy. In the first we measured photopic spectral sensitivity. Using a spatial two alternative forced choice task, two horses were required to discriminate a coloured circular patch on an achromatic background from a blank field over a range of wavelengths . The obtained spectral sensitivity function was consistent with the presence of two cone classes with predicted spectral peaks at 429 nm and 545 nm, respectively. In the second experiment we obtained wavelength discrimination functions. The same animals were required to make discriminations between a series of standard wavelengths and a series of comparison wavelengths across the spectrum. The resultant wavelength discrimination function showed a single minimum at approximately 480 nm, which is also consistent with the view that horses are dichromats. Key Words: Horse, colour vision, spectral sensitivity, wavelength discrimination
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Timney, B., & Keil, K. (1999). Local and global stereopsis in the horse. Vision Res, 39(10), 1861–1867.
Abstract: Although horses have laterally-placed eyes, there is substantial binocular overlap, allowing for the possibility that these animals have stereopsis. In the first experiment of the present study we measured local stereopsis by obtaining monocular and binocular depth thresholds for renal depth stimuli. On all measures, the horses' binocular performance was superior to their monocular. When depth thresholds were obtained, binocular thresholds were several times superior to those obtained monocularly, suggesting that the animals could use stereoscopic information when it was available. The binocular thresholds averaged about 15 min arc. In the second experiment we obtained evidence for the presence of global stereopsis by testing the animals' ability to discriminate between random-dot stereograms with and without consistent disparity information. When presented with such stimuli they showed a strong preference for the cyclopean equivalent of the positive stimulus with the real depth. These results provide the first behavioral demonstration of a full range of stereoscopic skills in a lateral-eyed mammal.
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Timney, B., & Keil, K. (1992). Visual acuity in the horse. Vis. Res., 32(12), 2289–2293.
Abstract: We assessed the ease with which horses could learn visual discriminations and measured their resolution acuity. We trained three horses to press their noses against one of two large wooden panels to receive a small food reward. Following training on a series of two-choice discrimination tasks, resolution acuity was measured. Although there was some variability between animals, the best acuity obtained was 23.3 c deg-1. Within the margin of error imposed by limited anatomical data, the obtained values are consistent with predictions based on retinal ganglion cell density estimates and posterior nodal distance/axial length ratios. They suggest that the resolution acuity of the horse is limited by ganglion cell density in the temporal portion of the narrow visual streak.
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Timney, B., & Macuda, T. (2001). Vision and hearing in horses. J Am Vet Med Assoc, 218(10), 1567–1574.
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