Individual differentiation in behaviour of honey bee workers (<Emphasis Type="Italic">Apis meltifera</Emphasis> L.)van der Blom, J.;
doi: 10.1007/BF01253898pmid: N/A
Summary Behavioural differentiation in honey bee workers has been the most important issue in papers on honey bee behaviour throughout the years. However, little is yet known about proximate factors leading to behavioural differentiation within worker honey bees of the same age group (idiosyncrasy). Although recently there have been many publications concerning the influence of genetic and physiological factors on worker behaviour, these factors do not provide proximate clues at the level of an individual. The aim of this paper is to describe behavioural differentiation within one age group of honey bee workers. These descriptions for more or less normal situations are necessary in order to make investigations with respect to the proximate factors leading to idiosyncrasy possible. Various methods have to be employed to describe and quantify these differences. The analysis of frequency distributions of involvement in a behaviour alone is usually not enough for this purpose. Significant idiosyncrasy has been found for “comb construction”, “allogrooming” and some behavioural acts which occur in queenless colonies: “involvement in aggressive interactions” (both as “aggressor” and as “victim”) and “staying in empty cells”. The distribution of the number of times workers were allogroomed never deviated from random distributions. Also workers' “involvement in visiting larvae in emergency queen cells” was mostly random.
Weight changes in adult hornets,<Emphasis Type="Italic">Vespa affinis</Emphasis> (Hymenoptera: Vespidae)Martin, S. J.;
doi: 10.1007/BF01253899pmid: N/A
Summary After sexuals emerge from their cells, they remain within the nest for 8–11 days (males) or 13–14 days (queens). During this time their weight increases (males 38 %, queens 40 %) due to the laying down of fat in the gaster. The weight of workers does not change over the same period. The fat is utilized by the queen during the 4–5 month overwintering period. When queens emerge in spring their weight is at its lowest, and they feed on nectar. Ovarian development, which was delayed during winter, now begins. During summer, queens again gain weight but this is now due to the development of the ovaries. The queen lives for about 1 year.
Memory and chemical communication in the orientation of two mass-recruiting ant speciesAron, S.;Beckers, R.;Deneubourg, J. L.;Pasteels, J. M.;
doi: 10.1007/BF01253900pmid: N/A
Summary The relative contribution of visual and chemical components in the orientation ofLasius niger andIridomyrmex humilis (Argentine ant) workers during mass recruitment to newly discovered food sources is analyzed over short time intervals. While both species orient in response to the trail pheromone, a large number ofL. niger foragers rapidly switch to a more individual orientation, based on their memory of environmental cues.I. humilis workers, on the other hand, predominantly use collective chemical cues. The effect of the number of reinforcements on visual learning and its interference with chemical communication show that olfactory cues always prevail in the Argentine ant. InL. niger, the proportion of ants orienting to visual cues is independent of the trail concentration. Detailed observations of the trail-laying behavior of individually marked foragers show that nearly all theI. humilis workers initially lay a trail, whereas only half theL. niger foragers do so. This proportion decreases considerably with the number of trips performed byL. niger workers, while remaining constant for the Argentine ants. These results are interpreted with respect to the species' behavioral ecology.
Landmark orientation during the approach to the nest in the stingless bee<Emphasis Type="Italic">Trigona (Tetragonisca) angustula</Emphasis> (Apidae, Meliponinae)Zeil, J.;Wittmann, D.;
doi: 10.1007/BF01253901pmid: N/A
Summary We displaced a small nest box containing stingless bees (Trigona (Tetragonisca)angustula) over distances of up to 1.6 meters in different directions and counted the numbers of returning foragers to measure the effects of this manipulation on the homing ability of bees. Bees find it hard to locate the nest box when it was displaced more than about 1 m backwards, forwards or sideways relative to the direction into which the nest entrance pointed. They do not find the nest when its height above ground is changed. The bees use landmarks in the vicinity of the nest to locate it: When the nest box is displaced and landmark positions are changed so that their angular position at the new nest site is the same as at the normal nest position their homing ability is less impaired than it is without changes in landmark positions. Our results show that the bees do not use the nest box itself as a landmark until they have approached the nest position to within about 1 meter with the aid of surrounding landmarks.
Defenders in the North American aphid<Emphasis Type="Italic">Pemphigus obesinymphae</Emphasis>Moran, N. A.;
doi: 10.1007/BF01253902pmid: N/A
Summary Gall-inhabiting individuals of the aphidPemphigus obesinymphae act as defenders, protecting other colony members against attack by dipteran and neuropteran larvae that are the primary predators of this species. As first instar nymphs, the progeny of the fundatrix patrol surfaces of galls and adjoining leaves. These first instar nymphs attack potential predators by mounting and grasping them and inserting their stylets. This defensive behavior, which is not exhibited by nymphs in later instars, appears to be effective in reducing predation. The fundatrix typically produces defenders throughout the extended gall-inhabiting phase, and her progeny delay development beyond the defensive first instar stage. By August, galls contain an average of 101 defenders. Early death of the fundatrix reduces the number of defenders in the gall and advances maturation of defenders into winged migrants, which otherwise mature in September and October. InPemphigus, defensive behavior by first instar nymphs appears to have evolved in the context of several types of derived life cycle, each involving an extended gall-inhabiting phase.
A latitudinal gradient in intensity of applying ant-repellent substance to the nest petiole in paper wasps (Hymenoptera: Vespidae)Kojima, Jun ichi;
doi: 10.1007/BF01253903pmid: N/A
Summary Observations on pre-emergence, single-foundress colonies of Japanese paper wasps (Polistes) revealed that there was a latitudinal gradient in intensity of application of an ant-repellent substance (secreted by the metasomal sternum VI glands) to the nest petiole. Thus the lower the latitude, the more frequently a foundress rubbed ant repellent onto the nest petiole. Estimation of potential ant predation on wasp brood using bait traps showed that there was a positive correlation between the frequency of rubbing and potential predation pressure from ants which are guided predominantly by substrate cues for foraging. There was also a latitudinal gradient in the degree of temporal association of rubbing behavior with foraging: the lower the latitude, the more closely foundress departure from the nest was associated with rubbing. Enlargement of the nest petiole by applying oral secretion potentially obliterated previous coats of ant repellent; however, this behavior was not always followed by rubbing behavior. The ant-repellent chemical barrier around the nest petiole may have evolved in tropical regions of the world as a defense against ant predation on wasp brood. I argue that as ant predation pressure diminishes towards the cooler regions, so does selection maintaining the behavioral sequence where foundress departure from the nest is preceded by rubbing behavior.
Long-term impact of orphaning on field colonies of<Emphasis Type="Italic">Coptotermes lacteus</Emphasis> (Froggatt) (Isoptera: Rhinotermitidae)Lenz, M.;Runko, S.;
doi: 10.1007/BF01253906pmid: N/A
Summary Colonies ofCoptotermes lacteus (Froggatt) from a site in coastal south-eastern Australia were experimentally orphaned in early 1989. Sample colonies were examined 3, 6, 12, 18, 24 or 30 months later for their caste composition, the presence of replacement reproductives and brood. All replacement reproductives were nymphoid neotenics. The number of functional (physogastric) females ranged from 1 to 27; this variability was maintained irrespective of the length of time between orphaning and inspection of the colonies. The average live mass of individual females stayed at 30 to 40 mg over the period of 6 to 30 months after orphaning in groups of more than five neotenic queens, but increased from 38 mg three months after orphaning to about 125 mg after 24 months in colonies headed by fewer than five neotenic females. The combined live mass of neotenic females could approach or even exceed that of primary queens. Two key features characterized experimentally and naturally orphaned, neotenic-headed colonies: (1) Nymphs differentiated in significant numbers all year round for a period of at least 30 months right from the time neotenics commenced breeding (in primary-headed colonies nymph production is strictly seasonal). (2) All or most nymphs were males (in primary-headed colonies the sex ratio of nymphs is more or less balanced). The mechanism(s) for achieving the male-biased sex ratio is (are) unknown. Even when colonies have resumed breeding with the help of neotenics, colony survival is not guaranteed. Under such circumstances the gene pool is best preserved if colonies were to raise and release large numbers of alates as potential founders of new colonies. By producing largely male nymphs orphaned colonies ensure outbreeding and may prevent competition (and its disruptive impact an breeding) between existing reproducing neotenic queens and newly differentiating female neotenics. Competition between male neotenics is unlikely to have any impact on the rate of brood production and therefore would not require a mechanism to prevent it from occurring.