Flower-naive honeybees Apis mellifera L. flying in an enclosure were tested for their colour preferences. Bees were rewarded once on an achromatic (grey, aluminium or hardboard), or on a chromatic (ultraviolet) disk. Since naive bees never alighted on colour stimuli alone, a scent was given in combination with colour. Their landings on twelve colour stimuli were recorded. Results after one reward ("first test") were analysed separately from those obtained after few rewards ("late tests"). 1) After pre-training to achromatic signals, bees preferred, in the first test, bee-uv-blue and bee-green colours. With increasing experience, the original preference pattern persisted but the choice of bee-blue and bee-green colours increased. 2) Neither colour distance of the test stimuli to the background or to the pre-training signal, nor their intensity, nor their green contrast, accounted for the colour choice of bees. Choices reflected innate preferences and were only associated with stimulus hue. 3) Bees learned very quickly the pre-trained chromatic stimulus, the original colour preferences being thus erased. 4) Colour preferences were strongly correlated with flower colour and its associated nectar reward, as measured in 154 flower species. 5) Colour preferences also resemble the wavelength dependence of colour learning demonstrated in experienced bees.

Experimental evidence is reported for flower-marking by honeybees (Apis mellifera ligustica) while they were foraging on an artificial patch of flowers yielding a continuous and equal flow of sucrose solution. Honeybees marked with scent and rejected all recently visited and nectar-depleted flowers. The short fade-out time of this scent allowed discrimination of flowers that temporarily provided no food. The repellent nature of this scent mark was demonstrated by the use of an air extractor connected to the patch; when the apparatus was turned on, the rejection behaviour disappeared. The movement pattern of foraging bees also contributed to foraging efficiency, as the probability of an immediate return to the flower just abandoned was very low. However, when a quick repeat visit took place, the presence of the repellent scent-mark promoted rapid rejection.

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1) When a thermal gradient (20-40° C) was established along a laboratory nest, Camponotus mus nurse workers showed a photoperiodic circadian rhythm of temperature preferences for brood rearing. Two different temperatures were daily selected to translocate the brood, i.e. 30.8° C selected at the middle of the photophase, and 27.5° C selected during the scotophase, 8 h later. 2) The daily temperature response of nurse workers consisted of paired high and low-temperature translocations, with a 8 hs-interval in between: high-temperature translocation was shown to be entrained by the photophase length, whereas low-temperature translocation was shown to be dependent on the precedent one. 3) Prey deprivation to the colony modified the brood transport behaviors resulting in translocations of only cocoons and large (ripe) larvae, stages in which the pupation processes are triggered. Small larvae and eggs remained located at 27.5° C. 4) Evaluation of pupa developmental time as well as percentage of pupa mortality at different temperature regimes allowed to construct an efficiency index relating pupa survival and cocoon developmental time. In the range of temperatures selected by nurses, the index reached its maximal values. 5) The ecological significance of these results is discussed.

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We tested the attraction of volatile compounds, produced by the aerobic growth of Saccharomyces cerevisiae on saccharose for Triatoma infestans. For these tests, we exploited the behavioural characteristic of these haematophagous insects of dropping when searching for food. In olfactometer assays, yeast cultures activated and attracted bugs as effectively as a mouse. The attraction of the cultures was significantly reduced when the carbon dioxide released was partially eliminated using potassium hydroxide. Yeast cultures were also tested as lures in a novel trap device. A baited device for trapping Chagas' disease vectors using the behavioural peculiarities of T. infestans and this simple attractant is described.

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