Abstract

Honey bee foragers use a “waggle dance” to inform nestmates about direction and distance to locations of attractive food. The sound and air flows generated by dancer's wing and abdominal vibrations have been implicated as important cues, but the decoding mechanisms for these dance messages are poorly understood. To understand the neural mechanisms of honey bee dance communication, we analyzed the anatomy of antenna and Johnston's organ (JO) in the pedicel of the antenna, as well as the mechanical and neural response characteristics of antenna and JO to acoustic stimuli, respectively. The honey bee JO consists of about 300–320 scolopidia connected with about 48 cuticular “knobs” around the circumference of the pedicel. Each scolopidium contains bipolar sensory neurons with both type I and II cilia. The mechanical sensitivities of the antennal flagellum are specifically high in response to low but not high intensity stimuli of 265–350 Hz frequencies. The structural characteristics of antenna but not JO neurons seem to be responsible for the non-linear responses of the flagellum in contrast to mosquito and fruit fly. The honey bee flagellum is a sensitive movement detector responding to 20 nm tip displacement, which is comparable to female mosquito. Furthermore, the JO neurons have the ability to preserve both frequency and temporal information of acoustic stimuli including the “waggle dance” sound. Intriguingly, the response of JO neurons was found to be age-dependent, demonstrating that the dance communication is only possible between aged foragers. These results suggest that the matured honey bee antennae and JO neurons are best tuned to detect 250–300 Hz sound generated during “waggle dance” from the distance in a dark hive, and that sufficient responses of the JO neurons are obtained by reducing the mechanical sensitivity of the flagellum in a near-field of dancer. This nonlinear effect brings about dynamic range compression in the honey bee auditory system.

Highlights

  • The honey bee (Apis mellifera) uses various chemical and physical stimuli for communication

  • We found that the flagellum can be moved at the joint between the pedicel and flagellum in response to acoustic stimuli

  • The sound-evoked vibrations of the flagellum at this joint and the relative position of the recording electrode strongly support the idea that sound-evoked compound potentials (SEP) are derived from the sensory neurons of the approximately 300 Johnston’s organ (JO) scolopidia

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Summary

Introduction

The honey bee (Apis mellifera) uses various chemical and physical stimuli for communication. One of the best-characterized forms of honey bee communication is the forager’s ‘‘waggle dance’’, which informs nestmates about the direction and distance to locations of attractive food [1] This dance consists of a series of alternating left-hand and right-hand loops, interspersed by a phase in which a dancer waggles her abdomen. Behavioral experiments demonstrated that honey bees can hear near-field sounds by detecting air-particle movements with Johnston’s organ (JO) located at the second segment (pedicel) of the antenna [9–11]. This hearing mechanism is ideal for the followers located only millimeters away from a dancer. These neurons project to the antennal mechanosensory region of the brain for further auditory processing

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