Abstract
Foragers of several species of stingless bees (Apidae; Meliponini), a group of eusocial bees comprising more than 400 mainly tropical species, produce pulsed thoracic vibrations inside the nest when returning from a successful foraging trip. These vibrations do not provide navigational information on the direction and distance of a food source. Instead, both their occurrence and their temporal pattern correlate with the net gain during a foraging trip. The vibrations are therefore considered important information for potential foragers about the profitability of a food patch. Their repeated presentation lowers the foraging threshold of potential food collectors. The vibrations are considered as an alerting signal, which increases the colony’s foraging activity. So far, nothing is known about how foragers of stingless bees perceive the pulsed thoracic vibrations of the recruiters. Yet, consideration of the corresponding receptors and their thresholds in honeybees suggests three possible pathways for their transmission to the nestmates: (1) the substrate (vibrations), (2) the air (air particle movements), and (3) direct physical contact (tactile stimuli). The corresponding differ significantly. Whereas substrate vibrations will reach receivers up to ten bee lengths away (medium-range transmission), air particle oscillations and direct vibrations can be detected only by bees very close to, or in contact with, the forager (short-range transmission). Thus, depending on the transmission pathway and the recipient’s sensory capacity, the signal generated by thoracic vibrations will have different meanings. Indeed, substrate vibrations attract both food processors and potential foragers to the vibrating bee, whereas air particle oscillations and direct contact vibrations, in addition to important olfactory and gustatory information, may well be used by prospective recruits to evaluate the profitability of the advertised food source. In contrast to the honeybee waggle dance vibrations, there is no indication in stingless bees of an air jet potentially providing directional information.
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Notes
- 1.
The individual variation in sugar intake of M. seminigra foragers collecting at an artificial food source was 3.32 mg (Hrncir et al. 2004b). Taking measurements in honeybees, which are of similar body size as M. seminigra, as reference, the bees spend 0.70 mg sugar for each 1,000 m of flight (Hanauer-Thieser and Nachtigall 1995). Nestmates receiving the thoracic vibrations of a forager would have to decide whether the forager loaded 3.32 mg less sugar at the food source (less energy intake) or spent more energy due to an additional 4,740 m of flight (consumption of additional 3.32 mg sugar). The energy budget, and thus thoracic vibrations reflecting it, would be the same under both conditions provided that thoracic vibrations are influenced to the same degree by energy intake and energy consumption.
- 2.
Wasps and bees produce thoracic vibrations when trying to escape from any form of confinement, such as when pushing through narrow nest entrances (Michener 2000), or when trying to escape from the grasp of predators or researchers (Esch and Wilson 1967; Schneider 1975; Larsen et al. 1986; Hrncir et al. 2008a). This form of thoracic vibrations (termed “disturbance buzzes”: Larsen et al. 1986; “annoyance buzzing”: Hrncir et al. 2008a) are known from both solitary bees (Colletes cunicularius: Larsen et al. 1986) and social bees (Bombini; Bombus terrestris: Schneider 1975; Meliponini; Melipona spp.: Esch and Wilson 1967; Hrncir et al. 2008a, b; Nunes-Silva 2011).
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Acknowledgments
Our sincere thanks go to Ronaldo Zucchi, Stefan Jarau, Dirk-Louis P. Schorkopf, and Veronika Schmidt whose participation, help, and discussion were decisive for many of the studies described in this chapter. Financial support for the research came from grants FAPESP (2006/50809-7) and CNPq (304722/2010-3) to MH, and FWF (P 14328, P 17530) to FGB.
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Hrncir, M., Barth, F.G. (2014). Vibratory Communication in Stingless Bees (Meliponini): The Challenge of Interpreting the Signals. In: Cocroft, R., Gogala, M., Hill, P., Wessel, A. (eds) Studying Vibrational Communication. Animal Signals and Communication, vol 3. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-43607-3_18
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