Visual generalization in honeybees: evidence of peak shift in color discrimination (original) (raw)
Related papers
Color distance derived from a receptor model of color vision in the honeybee
Biological Cybernetics, 1987
A model calculation is presented for investigating the domain between the two well-examined fields of color vision in the bee, i.e. choice behavior with respect to color stimuli, and photoreceptor physiology. Based on the properties of the receptors, the model explains quantitatively the results obtained in color discrimination experiments. The model predicts curved lines which connect the loci of most similar color stimuli in the receptor plane and makes quantitative predictions about the magnitude of the Bezold-Abney hue shift. A measure for color difference is derived from the number of the just-noticeabledifference (jnd) steps determined by the noise thresholds of the photoreceptor cells.
Fast learning but coarse discrimination of colours in restrained honeybees
Journal of Experimental Biology, 2009
Colours are quickly learnt by free-moving bees in operant conditioning settings. In the present study, we report a method using the classical conditioning of the proboscis extension response (PER) in restrained honeybees (Apis mellifera), which allows bees to learn colours after just a few training trials. We further analysed how visual learning and discrimination is influenced by the quality of a stimulus by systematically varying the chromatic and achromatic properties of the stimuli. Using differential conditioning, we found that faster colour discrimination learning was correlated with reduced colour similarity between stimuli. In experiments with both absolute and differential conditioning, restrained bees showed poor colour discrimination and broad generalisation. This result is in strong contrast to the well-demonstrated ability of bees to finely discriminate colours under freeflight conditions and raises further questions about the temporal and perceptual processes underlying the ability of bees to discriminate and learn colours in different behavioural contexts.
Detection of coloured stimuli by honeybees: minimum visual angles and receptor specific contrasts
Journal of Comparative Physiology A-neuroethology Sensory Neural and Behavioral Physiology, 1996
Honeybees Apis mellifera were trained to distinguish between the presence and the absence of a rewarded coloured spot, presented on a vertical, achromatic plane in a Y-maze. They were subsequently tested with different subtended visual angles of that spot, generated by different disk diameters and different distances from the decision point in the device. Bees were trained easily to detect bee-chromatic colours, but not an achromatic one. Chromatic contrast was not the only parameter allowing learning and, therefore, detection: α min, the subtended visual angle at which the bees detect a given stimulus with a probability P 0 = 0.6, was 5° for stimuli presenting both chromatic contrast and contrast for the green photoreceptors [i.e. excitation difference in the green photoreceptors, between target and background (green contrast)], and 15° for stimuli presenting chromatic but no green contrast. Our results suggest that green contrast can be utilized for target detection if target recognition has been established by means of the colour vision system. The green-contrast signal would be used as a far-distance signal for flower detection. This signal would always be detected before chromatic contrast during an approach flight and would be learned in compound with chromatic contrast, in a facilitation-like process.
Color constancy in the honeybee
The Journal of neuroscience : the official journal of the Society for Neuroscience, 1988
A multicolored display was illuminated by 3 bands of wavelengths corresponding to the maxima of the spectral sensitivities of the 3 types of photoreceptors found in the bee retina. The intensity of each band could be varied individually. The light fluxes emitted by the colored areas of the multicolored display were determined quantitatively. Free-flying honeybees were trained with sugar solution to choose one of the colored areas. The illumination was then changed in such a way that the light fluxes formerly emitted by the training area were now measured on another area. When the trained bees were tested under those conditions, they still chose the training area. The relative positions of the colored areas were changed in order to exclude learning of position. It is concluded that color vision in bees is, in a certain range, independent of the spectral content of the illumination. Model calculations show that the behavior observed in bees is consistent with the retinex theory (Land,...
Discrimination of coloured stimuli by honeybees: alternative use of achromatic and chromatic signals
Journal of Comparative Physiology A-neuroethology Sensory Neural and Behavioral Physiology, 1997
Using a Y-maze experimental set-up, honeybees Apis mellifera were trained to a coloured disc presented against an achromatic background. In subsequent tests they were given a choice between the trained disc and an alternative disc that differed either in its chromatic properties, or in the amount of achromatic green contrast that it produced against the background. Tests were conducted in two experimental situations: one in which discs subtended a visual angle of 30°(as viewed by the bee at the decision point in the Y-maze), and another in which the angle was 6.5°or 5°(depending on the experiment). At the visual angle of 30°, the bees' choice behaviour was governed by the differences in chromatic properties, and not by the differences in the amount of green contrast. With the 6.5°-and 5°discs, on the other hand, it was governed by the differences in the amount of green contrast, and not by the differences in chromatic properties. Consequently, in the present discrimination task, bees use either chromatic or achromatic cues, depending on the visual angle subtended by the stimuli at the eye. Results of a further experiment, in which the trained disc was tested against discs that produced various amounts of green contrast, confirm the above conclusion and show, in addition, that bees learn the green-contrast difference between a trained and a non-rewarded alternative.
Discrimination of coloured patterns by honeybees through chromatic and achromatic cues
Journal of Comparative Physiology A: Sensory, Neural, and Behavioral Physiology, 2002
We investigated pattern discrimination by worker honeybees, Apis mellifera, focusing on the roles of spectral cues and the angular size of patterns. Freeflying bees were trained to discriminate concentric patterns in a Y-maze. The rewarded pattern could be composed of either a cyan and a yellow colour, which presented both different chromatic and achromatic Lreceptor contrast, or an orange and a blue colour, which presented different chromatic cues, but the same L-receptor contrast. The non-rewarded alternative was either a single-coloured disc with the colour of the central disc or the surrounding ring of the pattern, a checkerboard pattern with non-resolvable squares, the reversed pattern, or the elements of the training pattern (disc or ring alone). Bees resolved and learned both colour elements in the rewarded patterns and their spatial properties. When the patterns subtended large visual angles, this discrimination used chromatic cues only. Patterns with yellow or orange central discs were generalised toward the yellow and orange colours, respectively. When the patterns subtended a visual angle close to the detection limit and L-receptor contrast was mediating discrimination, pattern perception was reduced: bees perceived only the pattern element with higher contrast.
Detection of coloured patterns by honeybees through chromatic and achromatic cues
Journal of Comparative Physiology A: Sensory, Neural, and Behavioral Physiology, 2001
We asked whether the detection range of twocoloured centre-surround patterns diers from that of single-coloured targets. Honeybees Apis mellifera were trained to distinguish between the presence and absence of a single-coloured disc or a coloured pattern at different visual angles. The patterns presented colours which were either dierent in chromatic and L-receptor contrasts to the background, equal in chromatic but dierent in L-receptor contrasts, or vice-versa. Patterns with colours presenting only chromatic contrast were also tested. Patterns with higher L-receptor contrast in its outer than in its inner element were better detected than patterns with a reversed L-contrast distribution. However, both were detected worse than single-coloured discs of the respective colours. When the L-receptor contrast was the same for both elements, the detection range of the two-coloured and single-coloured targets was the same. Patterns whose colours lacked L-receptor contrast were detected just as single-coloured targets of the same colours. These results demonstrate that both chromatic and L-receptor contrasts mediate the detec-tion of coloured patterns and that particular distributions of L-receptor contrast within a target are better detected than others. This ®nding is consistent with the intervention of neurons with centre-surround receptive ®elds in the detection of coloured patterns.
Mechanisms, functions and ecology of colour vision in the honeybee
Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology, 2014
Research in the honeybee has laid the foundations for our understanding of insect colour vision. The trichromatic colour vision of honeybees shares fundamental properties with primate and human colour perception, such as colour constancy, colour opponency, segregation of colour and brightness coding. Laborious efforts to reconstruct the colour vision pathway in the honeybee have provided detailed descriptions of neural connectivity and the properties of photoreceptors and interneurons in the optic lobes of the bee brain. The modelling of colour perception advanced with the establishment of colour discrimination models that were based on experimental data, the Colour-Opponent Coding and Receptor Noise-Limited models, which are important tools for the quantitative assessment of bee colour vision and colour-guided behaviours. Major insights into the visual ecology of bees have been gained combining behavioural experiments and quantitative modelling, and asking how bee vision has influe...
Arthropod-Plant Interactions, 2008
It has long been assumed that bees cannot see red. However, bees visit red flowers, and the visual spectral sensitivity of bees extends into wavelengths to provide sensitivity to such flowers. We thus investigated whether bees can discriminate stimuli reflecting wavelengths above 560 nm, i.e., which appear orange and red to a human observer. Flowers do not reflect monochromatic (single wavelength) light; specifically orange and red flowers have reflectance patterns which are step functions, we thus used colored stimuli with such reflectance patterns. We first conditioned honey bees Apis mellifera to detect six stimuli reflecting light mostly above 560 nm and found that bees learned to detect only stimuli which were perceptually very different from a bee achromatic background. In a second experiment we conditioned bees to discriminate stimuli from a salient, negative (un-rewarded) yellow stimulus. In subsequent unrewarded tests we presented the bees with the trained situation and with five other tests in which the trained stimulus was presented against a novel one. We found that bees learned to discriminate the positive from the negative stimulus, and could unambiguously discriminate eight out of fifteen stimulus pairs. The performance of bees was positively correlated with differences between the trained and the novel stimulus in the receptor contrast for the long-wavelength bee photoreceptor and in the color distance (calculated using two models of the honeybee colors space). We found that the differential conditioning resulted in a concurrent inhibitory conditioning of the negative stimulus, which might have improved discrimination of stimuli which are perceptually similar. These results show that bees can detect long wavelength stimuli which appear reddish to a human observer. The mechanisms underlying discrimination of these stimuli are discussed.
Journal of Comparative Physiology A, 2014
Your article is protected by copyright and all rights are held exclusively by Springer-Verlag Berlin Heidelberg. This e-offprint is for personal use only and shall not be selfarchived in electronic repositories. If you wish to self-archive your article, please use the accepted manuscript version for posting on your own website. You may further deposit the accepted manuscript version in any repository, provided it is only made publicly available 12 months after official publication or later and provided acknowledgement is given to the original source of publication and a link is inserted to the published article on Springer's website. The link must be accompanied by the following text: "The final publication is available at link.springer.com". 1 3 J Comp Physiol A