1. Substrate-borne vibration signals play an important role in the life of the fiddler crabUca pugilator. In this study we investigated how a vibration signal is transmitted through the legs and body of the freely standing live crab and how it is modified on its way to the sites of the crab's vibration-receptive organs. 2. An optical technique, Laser Doppler Vibrometry (LDV), was used to measure the motion of the substrate (the input signal) and the motion of the dactylopodite, carpopodite, meropodite and carapax (the output signals). The output motion was compared with the input motion to determine the transfer function at each of the measured points over the frequency range of 10 to 1,000 Hz. 3. In response to a single input vibration pulse with an energy spectrum similar to that of a rap of a male fiddler crab, points on the crab showed amplification of the low-frequency components (up to 25–250 Hz) with no amplification or else attenuation in a mid-frequency range (from 25–250 to about 800 Hz), and then a range of less attenuation or slight amplification above about 800 Hz (Fig. 4). The amplification and attenuation effects tended to be more pronounced the further away from the leg tip the measurement point was. Maximal low-frequency amplification ranged from 8 to 32 dB, maximal mid-frequency attenuation between −7 and −33 dB, with higher values closer to the carapax. The vibration transfer characteristics were essentially independent of the input amplitude over the biologically relevant intensity range (Fig. 5). 4. When a train of input pulses was given at about the drumming rate of maleUca pugilator the transfer function changed during the train, with transmission of the first few impulses being as described above and that of later impulses being more ‘sharply tuned’, that is, with the low-frequency amplification range being narrower (Fig. 6). This change in transmission is reproducibly accompanied by small active postural changes of the crab (‘alerting reaction’). 5. Animals resting in body-contact with the substrate rather than in an upright ‘alert’ stance showed very different transmission characteristics with much less modification of the signal between substrate and carapax (Fig. 7). 6. These results are compared with the known spectral energy distribution of crab drumming signals. It is concluded, that the described transmission characteristics of the crab leg emphasize the specific communication signals while at the same time damping noise vibrations.
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