Extension of the proboscis was conditioned in restrained honeybees with odor as the conditioned stimulus (CS) and sucrose solution-delivered to the antenna (to elicit extension of the proboscis) and then to the proboscis itselfas the unconditioned stimulus (US). In a first series of experiments, acquisition was found to be very rapid, both in massed and in spaced trials; its associative basis was established by differential conditioning and by an explicitly unpaired control procedure (which produced marked resistance to acquisition in subsequent paired training); and both extinction and spontaneous recovery in massed trials were demonstrated. In a series of experiments on the nature of the US, eliminating the proboscis component was found to lower the asymptotic level of performance, whereas eliminating the antennal component was without effect; reducing the concentration of sucrose from 20% to 7% slowed acquisition but did not lower the asymptotic level of performance; and secondorder conditioning was demonstrated. In a series of experiments on the role of the US, an omission contingency designed to eliminate adventitious response-reinforcer contiguity was found to have no adverse effect on acquisition. In a series of experiments designed to analyze the resistance to acquisition found after explicitly unpaired training in the first experiments, no significant effect was found of prior exposure either to the CS alone or to the US alone, although the unpaired procedure again produced substantial resistance that was shown to be due to inhibition rather than to inattention; extinction after paired training was found to be facilitated by unpaired presentations of the US, The relation between these results for honeybees and those of analogous experiments with vertebrates is considered.

Spectral sensitivity functions S(lambda) of single photoreceptor cells in 43 different hymenopteran species were measured intracellularly with the fast spectral scan method. The distribution of maximal sensitivity values (lambda max) shows 3 major peaks at 340 nm, 430 nm and 535 nm and a small peak at 600 nm. Predictions about the colour vision systems of the different hymenopteran species are derived from the spectral sensitivities by application of a receptor model of colour vision and a model of two colour opponent channels. Most of the species have a trichromatic colour vision system. Although the S(lambda) functions are quite similar, the predicted colour discriminability curves differ in their relative height of best discriminability in the UV-blue or blue-green area of the spectrum, indicating that relatively small differences in the S(lambda) functions may have considerable effects on colour discriminability. Four of the hymenopteran insects tested contain an additional R-receptor with maximal sensitivity around 600 nm. The R-receptor of the solitary bee Callonychium petuniae is based on a pigment (P596) with a long lambda max, whereas in the sawfly Tenthredo campestris the G-receptor appears to act as filter to a pigment (P570), shifting its lambda max value to a longer wavelength and narrowing its bandwidth. Evolutionary and life history constraints (e.g. phylogenetic relatedness, social or solitary life, general or specialized feeding behaviour) appear to have no effect on the S(lambda) functions. The only effect is found in UV receptors, for which lambda max values at longer wavelengths are found in bees flying predominantly within the forest.

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Co.rre1 atcon betvveen panems 1n c a Rd d. r = 0.92 (P < 0.001). B, Time courses of calcium• signals at selected glomeruli {dlfferern experinienl) a, Odours .elicit specific s1gnals upon s tiffUJiat•Oi1 (bar). b. Hexaoollcads to successive activat•on of dif.erent regions (see Inset) 2 8 5