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| Volume 1, Number 2, Article 2, Pages 80-87 |
doi:10.1167/1.2.2 |
http://journalofvision.org/1/2/2/ |
ISSN 1534-7362 |
Photopigment basis for dichromatic color vision in the horse
Joseph Carroll |
Department of Cell Biology, Neurobiology & Anatomy, Medical College of Wisconsin, Milwaukee, WI, USA |
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Christopher J. Murphy |
Department of Surgical Sciences, School of Veterinary Medicine, and Department of Ophthalmology and Visual Sciences, School of Medicine, University of Wisconsin-Madison, Madison, WI, USA |
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Maureen Neitz |
Departments of Ophthalmology and Cell Biology, Neurobiology and Anatomy, Medical College of Wisconsin, Milwaukee, WI, USA |
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James N. Ver Hoeve |
Department of Ophthalmology and Visual Sciences, School of Medicine, University of Wisconsin-Madison, Madison, WI, USA |
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Jay Neitz |
Departments of Cell Biology, Neurobiology and Anatomy, and Ophthalmology, Medical College of Wisconsin, Milwaukee, WI, USA |
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Abstract
Horses, like other ungulates, are active in the day, at dusk, dawn, and night; and, they have eyes designed to have both high sensitivity for vision in dim light and good visual acuity under higher light levels (Walls, 1942). Typically, daytime activity is associated with the presence of multiple cone classes and color-vision capacity (Jacobs, 1993). Previous studies in other ungulates, such as pigs, goats, cows, sheep and deer, have shown that they have two spectrally different cone types, and hence, at least the photopigment basis for dichromatic color vision (Neitz & Jacobs, 1989; Jacobs, Deegan II, Neitz, Murphy, Miller, & Marchinton, 1994; Jacobs, Deegan II, & Neitz, 1998). Here, electroretinogram flicker photometry was used to measure the spectral sensitivities of the cones in the domestic horse (Equus caballus). Two distinct spectral mechanisms were identified and are consistent with the presence of a short-wavelength-sensitive (S) and a middle-to-long-wavelength-sensitive (M/L) cone. The spectral sensitivity of the S cone was estimated to have a peak of 428 nm, while the M/L cone had a peak of 539 nm. These two cone types would provide the basis for dichromatic color vision consistent with recent results from behavioral testing of horses (Macuda & Timney, 1999; Macuda & Timney, 2000; Timney & Macuda, 2001). The spectral peak of the M/L cone photopigment measured here, in vivo, is similar to that obtained when the gene was sequenced, cloned, and expressed in vitro (Yokoyama & Radlwimmer, 1999). Of the ungulates that have been studied to date, all have the photopigment basis for dichromatic color vision; however, they differ considerably from one another in the spectral tuning of their cone pigments. These differences may represent adaptations to the different visual requirements of different species.
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