scholarly journals Színfolt a Kanonoksoron = Colour Patch Along the Kanonoksor

Metszet ◽  
2020 ◽  
Vol 11 (3) ◽  
pp. 50-55
Author(s):  
Katalin Getto
Keyword(s):  
1993 ◽  
Vol 46 (1) ◽  
pp. 51-82 ◽  
Author(s):  
Harold Pashler ◽  
Mark Carrier ◽  
James Hoffman

Four dual-task experiments required a speeded manual choice response to a tone in a close temporal proximity to a saccadic eye movement task. In Experiment 1, subjects made a saccade towards a single transient; in Experiment 2, a red and a green colour patch were presented to left and right, and the saccade was to which ever patch was the pre-specified target colour. There was some slowing of the eye movement, but neither task combination showed typical dual-task interference (the “psychological refractory effect”). However, more interference was observed when the direction of the saccade depended on whether a central colour patch was red or green, or when the saccade was directed towards the numerically higher of two large digits presented to the left and the right. Experiment 5 examined a vocal second task, for comparison. The findings might reflect the fact that eye movements can be directed by two separate brain systems–-the superior colliculus and the frontal eye fields; commands from the latter but not the former may be delayed by simultaneous unrelated sensorimotor tasks.


The author describes a modification of his colour patch apparatus, in which two spectra are produced by the same beam that passes through the collimator and prisms. With this apparatus two distinct patches of pure or mixed colours can be placed side by side upon a white screen, and when a set of three slits is placed in each spectrum, mixtures in one spectrum can be matched with mixtures in the other, or with pure colours and white combined. This new apparatus, in which also the positions of the slits in the two spectra could be most accurately determined, was used for a redetermination of the visual sensation curves.


2002 ◽  
Vol 55 (3) ◽  
pp. 917-936 ◽  
Author(s):  
Tony Ro ◽  
Liana Machado ◽  
Nancy Kanwisher ◽  
Robert D. Rafal

The role of covert orienting of attention in response channel activation was examined using the flanker interference and precueing paradigms. Four experiments assessed the influence of distractors on the discrimination of a target colour patch under cueing conditions (three with non-informative, exogenous cues and one with informative, endogenous cues) that modulated attention at the flanker or target locations. Across all of the experiments, the amount of interference generated by the distractors was not modulated by the facilitation and inhibition of return induced by spatial attention precues. These results are consistent with previous reports of patients with neglect, which demonstrated that flanker interference proceeds at unattended locations (Audet, Bub, & Lecours, 1991; Cohen, Ivry, Rafal, & Kohn, 1995), and they suggest that response channel activation can occur independently from spatial attention.


A Simple Test .—In Parts II and III of this series of papers I have indicated several methods of giving a quantitative value to the amount of green or red sensation which exists in the incomplete green- or red-blind eye as compared with the normal eye. I need not summarise what has already appeared at recent dates in the ‘Proceedings’ of the Royal Society, but I will at once explain a very simple test which gives quantitative measures of the sensations in incomplete colour-blindness. In my last paper of the series a table is given of the luminosity of the arc spectrum and the percentage composition of the tabulated rays of the spectrum, and from the same table the amount of white which exists in these several rays can readily be calculated. Owing to change in hue which white causes in a mixture of a pure red with a green ray I pointed out that the match of the D line by two such rays is open to error, not considerable perhaps, but still appreciable. In my communication “On the Change of Hue of Spectrum Colours by Dilution with White Light, it was shown that the change in hue at the point where the two curves of red and green sensations cut when their areas are made equal is nil . For reasons given later it may also be mentioned that a ray at this point when mixed with a blue where the same red and green sensation curves cut, will, with proper adjustment of the widths of the slits, match the white of the reflected beam of the arc light. The same happens for any other source of light if the curves of equal areas are calculated for such a light. The position of the point of intersection in the yellow part of the spectrum varies with the kind of light forming the spectrum. Looking at the table it will be seen that from S. S. N. 50 to the extreme red there is no blue sensation present in measurable quantities. Suppose that in a beam of the arc spectrum a cell containing a saturated solution of potassium chromate of (say) ¾ inch in thickness is placed; the beam becomes yellow with very little blue present. If a slit is caused to traverse the spectrum in the colour patch apparatus a position will be found for it which exactly matches the hue of the white light which passes through the chromate solution, and will be at S. S. N. 49·6 or λ 5828 to the normal eye. This, like other rays, contains a fixed ratio of green to red sensations, but no blue which is measurable. Making the red sensation unity it will be found that the green sensation present is 0·385. A table of the ratio of red to green sensation (making red unity) for the standard spectrum scale is annexed, as is also a table of wave-lengths with the like ratios:—


2018 ◽  
Author(s):  
John A. Endler ◽  
Gemma L. Cole ◽  
Alexandrea Kranz

AbstractColour patterns are used by many species to make decisions that ultimately affect their Darwinian fitness. Colour patterns consist of a mosaic of patches that differ in geometry and visual properties. Although traditionally pattern geometry and colour patch visual properties are analysed separately, these components are likely to work together as a functional unit. Despite this, the combined effect of patch visual properties, patch geometry, and the effects of the patch boundaries on animal visual systems, behaviour and fitness are relatively unexplored. Here we describe Boundary Strength Analysis (BSA), a novel way to combine the geometry of the edges (boundaries among the patch classes) with the receptor noise estimate (ΔS) of the intensity of the edges. The method is based upon known properties of vertebrate and invertebrate retinas. The mean and SD of ΔS (mΔS, sΔS) of a colour pattern can be obtained by weighting each edge class ΔS by its length, separately for chromatic and achromatic ΔS. This assumes those colour patterns, or parts of the patterns used in signalling, with larger mΔS and sΔS are more stimulating and hence more salient to the viewers. BSA can be used to examine both colour patterns and visual backgrounds. BSA was successful in assessing the estimated conspicuousness of colour pattern variants in two species, guppies (Poecilia reticulata) and Gouldian finches (Erythrura gouldiae), both polymorphic for patch colour, luminance and geometry. The pattern difference between chromatic and achromatic edges in both species reveals the possibility that chromatic and achromatic edges could function differently. BSA can be applied to any colour pattern used in intraspecific and interspecific behaviour. Seven predictions and four questions about colour patterns are presented.


In “Colour Photometry, Part III,” ‘Phil. Trans.,' 1892, and “On the Sensitiveness of the Retina to Light and Colour,” ‘Phil. Trans.,’ 1897, a discussion on the extinction of light by a “dark-adapted” eye is given. Since the latter date, a large number of experiments have been made by myself and others on the extinction of light when the retina as a whole has been stimulated by illumination of white or coloured light. In this communication the results obtained when the stimulation is by white light are described. In the two papers above referred to the apparatus used when the eye was dark-adapted is described, but for the observations made with an illuminated retina a modification had to be made. A description of one form, which answered as well as any other form, is given. BB is a box as in fig. 1. At the end of the box is cut a hole ¾ inch in diameter and against it, but inside, is placed a 4-inch disc of white matt paper, in the centre of which is cut a ½-inch circular hole. Behind the box is a second end AA separated from the first by a couple of inches. Opposite the aperture at the first end of the box is cut a circular aperture 1 inch in diameter, against which is placed a piece of doubly-ground white glass, and if necessary a second piece can be placed behind it. The ray of the spectrum from the colour-patch apparatus can be reflected from a mirror M on to the ground glasses at d . The 4-inch white disc is illuminated by the white reflected beam of the same apparatus (or by any other light) through an aperture CC cut in the side of the box. This beam partly goes through the aperture at the end of the box and falls on G, a blackened surface, and is completely hidden from the eye end E. At the side of CC a small metal disc can be placed, which casts a sharp black image on the white disc, as shown in fig. 2. This may be taken as a measure of the blackness to be matched when extinguishing the light from the colour.


2012 ◽  
Vol 15 (4) ◽  
pp. 771-781 ◽  
Author(s):  
NIHARIKA SINGH ◽  
RAMESH KUMAR MISHRA

Though many previous studies have reported enhanced cognitive control in bilinguals, few have investigated if such control is modulated by language proficiency. Here, we examined the inhibitory control of high and low proficient Hindi–English bilinguals on an oculomotor Stroop task. Subjects were asked to make a saccade as fast as possible towards the appropriate colour patch among competitors and distractors suppressing an eye movement evoked by the meaning of the word. High proficient bilinguals quickly oriented their attention towards the correct colour patch while effectively controlling the Stroop interference compared with low proficient subjects, on both colour and direction words. High proficient bilinguals also had fewer saccadic errors and demonstrated overall faster saccadic latency on all trial types. The results provide strong evidence for enhanced oculomotor control in proficient bilinguals compared with the less proficient ones.


2017 ◽  
Vol 8 (11) ◽  
pp. 1585-1593 ◽  
Author(s):  
Arnaud Badiane ◽  
Guillem Pérez i de Lanuza ◽  
María del Carmen García‐Custodio ◽  
Pau Carazo ◽  
Enrique Font

2021 ◽  
Vol 288 (1947) ◽  
Author(s):  
Cristina Romero-Diaz ◽  
Jake A. Pruett ◽  
Stephanie M. Campos ◽  
Alison G. Ossip-Drahos ◽  
J. Jaime Zúñiga-Vega ◽  
...  

Behavioural responses to communicative signals combine input from multiple sensory modalities and signal compensation theory predicts that evolutionary shifts in one sensory modality could impact the response to signals in other sensory modalities. Here, we conducted two types of field experiments with 11 species spread across the lizard genus Sceloporus to test the hypothesis that the loss of visual signal elements affects behavioural responses to a chemical signal (conspecific scents) or to a predominantly visual signal (a conspecific lizard), both of which are used in intraspecific communication. We found that three species that have independently lost a visual signal trait, a colourful belly patch, responded to conspecific scents with increased chemosensory behaviour compared to a chemical control, while species with the belly patch did not. However, most species, with and without the belly patch, responded to live conspecifics with increased visual displays of similar magnitude. While aggressive responses to visual stimuli are taxonomically widespread in Sceloporus , our results suggest that increased chemosensory response behaviour is linked to colour patch loss. Thus, interactions across sensory modalities could constrain the evolution of complex signalling phenotypes, thereby influencing signal diversity.


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