Foraging in the ant Camponotus mus: nectar-intake rate and crop filling depend on colony starvation.

The effects of colony starvation on the dynamics of nectar collection were studied in individual workers of the ant Camponotus mus. A laboratory colony was first deprived of carbohydrates for 15days, and thereafter fed daily ad libitum with diluted honey until satiation. During these two successive experimental phases, the probability of feeding, crop filling and fluid-intake rates were recorded daily for individual foragers collecting a 10% (w/w) sucrose solution. The feeding responses of individuals varied with the nutritional state of the colony. When the colony was deprived of sugar, acceptance of the sucrose solution was higher than under satiation. Feeding time increased with increasing starvation. During deprivation workers fed nearly continuously on the solution, whereas a number of feeding interruptions occurred under satiation. Crop filling also increased with increasing starvation, and showed a marked decrease when the colony was satiated. Fluid-intake rate during the deprivation phase was roughly twice that during the satiation phase. This matched well with the difference in sucking frequency recorded during ingestion in satiated and starved workers, which was also higher during starvation. Results indicate that the responsiveness of foragers, determined by the nutritional state of the colony, influenced both foraging decisions and the dynamics of fluid intake.

[1]  T. Daniel,et al.  On the mechanics and energetics of nectar feeding in butterflies. , 1979, Journal of theoretical biology.

[2]  R. R. Brenner,et al.  Chagas' disease vectors , 1987 .

[3]  R. Matthews,et al.  Ants. , 1898, Science.

[4]  R. C. Weast CRC Handbook of Chemistry and Physics , 1973 .

[5]  D. Cosens,et al.  The dynamic nature of the activities of the wood ant Formica aquilonia foraging to static food resources within a laboratory habitat , 1986 .

[6]  W. Farina,et al.  Food-exchange by foragers in the hive – a means of communication among honey bees? , 1996, Behavioral Ecology and Sociobiology.

[7]  M. H. Nitecki,et al.  Biochemical Aspects of Evolutionary Biology , 1983 .

[8]  D. M. Wilson Central nervous mechanisms for the generation of rhythmic behaviour in arthropods. , 1966, Symposia of the Society for Experimental Biology.

[9]  H. C. Bennet-Clark,et al.  NEGATIVE PRESSURES PRODUCED IN THE PHARYNGEAL PUMP OF THE BLOOD-SUCKING BUG, RHODNIUS PROLIXUS , 1963 .

[10]  F. Roces,et al.  Nectar feeding by the ant Camponotus mus: intake rate and crop filling as a function of sucrose concentration. , 1998, Journal of insect physiology.

[11]  M. Rice Cibarial stretch receptors in the tsetse fly (Glossina austeni) and the blowfly (Calliphora erythrocephala). , 1970, Journal of insect physiology.

[12]  R. Snodgrass,et al.  Anatomy of the Honey Bee , 1956 .

[13]  J. J. Smith,et al.  Effect of diet viscosity on the operation of the pharyngeal pump in the blood-feeding bug Rhodnius prolixus. , 1979, The Journal of experimental biology.

[14]  J. Núñez,et al.  Honeybee Foraging Strategies at a Food Source in Relation to its Distance from the Hive and the Rate of Sugar Flow , 1982 .

[15]  J.J.B. Smith,et al.  Feeding in Rhodnius prolixus: Responses to artificial diets as revealed by changes in electrical resistance , 1970 .

[16]  B. Bentley,et al.  The Biology of Nectaries , 1983 .

[17]  Martin Giurfa,et al.  Motivation and regulation of honey bee foraging , 1996 .

[18]  D. McFarland Feedback mechanisms in animal behaviour , 1971 .