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K A Fritsches

Publications and source records attributed to K A Fritsches.

4 recordsLinked to original sources
PubMed2000

Colour vision in billfish.

Members of the billfish family are highly visual predatory teleosts inhabiting the open ocean. Little is known about their visual abilities in detail, but past studies have indicated that these fishes were likely to be monochromats. This study, however, presents evidence of two anatomically distinct cone types in billfish. The cells are arranged in a regular mosaic pattern of single and twin cones as in many fishes, and this arrangement suggests that the different cone types also show different spectral sensitivity, which is the basis for colour vision. First measurements using microspectrophotometry (MSP) revealed a peak absorption of the rod pigment at 484 nm, indicating that MSP, despite technical difficulties, will be a decisive tool in proving colour vision in these offshore fishes. When hunting, billfish such as the sailfish flash bright blue bars on their sides. This colour reflects largely in ultraviolet (UV) light at 350 nm as revealed by spectrophotometric measurements. Billfish lenses block light of wavelengths below 400 nm, presumably rendering the animal blind to the UV component of its own body colour. Interestingly, at least two prey species of billfish have lenses transmitting light in the UV waveband and are therefore likely to perceive a large fraction of the UV peak found in the blue bar of the sailfish. The possible biological significance of this finding is discussed.

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PubMed1997

The second visual area in the marmoset monkey: visuotopic organisation, magnification factors, architectonical boundaries, and modularity.

The organisation of the second visual area (V2) in marmoset monkeys was studied by means of extracellular recordings of responses to visual stimulation and examination of myelin- and cytochrome oxidase-stained sections. Area V2 forms a continuous cortical belt of variable width (1-2 mm adjacent to the foveal representation of V1, and 3-3.5 mm near the midline and on the tentorial surface) bordering V1 on the lateral, dorsal, medial, and tentorial surfaces of the occipital lobe. The total surface area of V2 is approximately 100 mm2, or about 50% of the surface area of V1 in the same individuals. In each hemisphere, the receptive fields of V2 neurones cover the entire contralateral visual hemifield, forming an ordered visuotopic representation. As in other simians, the dorsal and ventral halves of V2 represent the lower and upper contralateral quadrants, respectively, with little invasion of the ipsilateral hemifield. The representation of the vertical meridian forms the caudal border of V2, with V1, whereas a field discontinuity approximately coincident with the horizontal meridian forms the rostral border of V2, with other visually responsive areas. The bridge of cortex connecting dorsal and ventral V2 contains neurones with receptive fields centred within 1 degree of the centre of the fovea. The visuotopy, size, shape and location of V2 show little variation among individuals. Analysis of cortical magnification factor (CMF) revealed that the V2 map of the visual field is highly anisotropic: for any given eccentricity, the CMF is approximately twice as large in the dimension parallel to the V1/V2 border as it is perpendicular to this border. Moreover, comparison of V2 and V1 in the same individuals demonstrated that the representation of the central visual field is emphasised in V2, relative to V1. Approximately half of the surface area of V2 is dedicated to the representation of the central 5 degrees of the visual field. Calculations based on the CMF, receptive field scatter, and receptive field size revealed that the point-image size measured parallel to the V1/V2 border (2-3 mm) equals the width of a full cycle of cytochrome oxidase stripes in V2, suggesting a close correspondence between physiological and anatomical estimates of the dimensions of modular components in this area.

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PubMed1996

Visuotopic organisation of striate cortex in the marmoset monkey (Callithrix jacchus).

The visuotopic organisation of the primary visual cortex (V1) was studied by extracellular recordings in adult male marmosets (Callithrix jacchus) that were anaesthetised with sufentanil/nitrous oxide and paralysed with pancuronium bromide. Extensive sampling of the occipital region in four individuals and partial coverage of V1 in five others allowed not only the establishment of the normal visuotopy but also the study of interindividual variability. As in other primates, there was a single, continuous map of the contralateral hemifield in V1, with the upper visual quadrant represented ventrally and the lower quadrant represented dorsally. The surface area of V1, which was measured in two-dimensional reconstructions of the cortical surface, varied from 192 to 217 mm2. There was a marked emphasis on the representation of the foveal and parafoveal visual fields: the representation of the central 5 degrees of the visual field occupied 36-39% of the surface area of V1, whereas the central 10 degrees occupied 57-59%. No asymmetry between the representations of the upper and lower quadrants was apparent. The visual topography of V1 was highly consistent between individuals, relative to both sulcal landmarks and stereotaxic coordinates. The entire contralateral hemifield was represented in V1; in addition, neurones with receptive fields whose borders invaded the ipsilateral hemifield were observed within V1, less than 800 microns from the V1/V2 boundary. The total invasion of the ipsilateral hemifield was less than 0.5 degree at the centre of the fovea but reached 8 degrees at the periphery of the vertical meridian. Our results demonstrate that the organisation of V1 is similar in diurnal New and Old World simians, despite major variations in size, ecological niche, and timing of postnatal development across species.

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