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Bush crickets are a model group for testing hypotheses in sexual selection, but much of the information is based on laboratory observations on wingless or short-winged species, which may restrict their generality. Here we describe aspects of the mating behaviour of the long-winged European bush cricket Phaneroptera falcata (Poda, 1761). Both in the laboratory and the field, diel calling followed a normal, though slightly left-skewed distribution, peaking about three hours after sunset or lights-off. Under bright greenhouse conditions, when the light was suddenly switched off, calling occurred only after the onset of darkness. Decreasing light intensity may trigger the start of calling activity. In the field, calling decreased from midnight onwards, which may be related to a decrease in temperature. The sequence of events during copulation was identical in the laboratory and the field. However, in two of 14 copulations documented in the field, a pre-copulatory behaviour was observed that resembled the putative removal and ingestion of rival sperm. Previous suggestions that P. falcata (Poda) is monogamous are rejected on the basis of both laboratory and field results. In the laboratory males and females mated every 2.3 and 3.6 days, respectively. We introduce a simple way to calculate the average frequency of mating in the field, based on the observation that at any one time 3% of all the individuals are recorded mating and copulation lasts 15 min. We estimate that on average P. falcata (Poda) mates once per day. More generally, our results show it is important for evolutionary conclusions to measure behaviourial data in the field. [ABSTRACT FROM AUTHOR]

In bush-crickets, males produce a calling song to announce their presence to females. Females ready to mate respond either by a phonotactic approach or signal their presence acoustically by establishing a kind of duet. This duetting behaviour is typical of phaneropterid bush-crickets, of which many species in Europe are flightless. In the long-winged genus Phaneroptera, the females also respond acoustically to the male calling song, which is quite similar in the three west European species in this genus. After acoustical contact, however, the behaviour of males and females of the three species differ markedly. In P. nana, males and females engage in a duet in which the female responds to each syllable of the male song (and he approaches her). In P. falcata, the female only responds to certain elements of the male song that are produced at long intervals. However, after her response the male does not change its song or its position, but often increases its singing activity (and the female approaches him). In P. sparsa the female only responds to particular, very complicated and soft elements of the male song, which are typically repeated at intervals of several to many minutes. After hearing the response, the male drastically changes its song by producing only the soft elements. These parts of the song contain syllables with a unique spectral composition and others that may threaten eavesdropping rivals. In this species both sexes probably move towards each other during mate localization. At present, we can only speculate about the adaptive nature of the different strategies. [ABSTRACT FROM AUTHOR]

In bush-crickets, males produce a calling song to announce their presence to females. Females ready to mate respond either by a phonotactic approach or signal their presence acoustically by establishing a kind of duet. This duetting behaviour is typical of phaneropterid bush-crickets, of which many species in Europe are flightless. In the long-winged genus Phaneroptera, the females also respond acoustically to the male calling song, which is quite similar in the three west European species in this genus. After acoustical contact, however, the behaviour of males and females of the three species differ markedly. In P. nana, males and females engage in a duet in which the female responds to each syllable of the male song (and he approaches her). In P. falcata, the female only responds to certain elements of the male song that are produced at long intervals. However, after her response the male does not change its song or its position, but often increases its singing activity (and the female approaches him). In P. sparsa the female only responds to particular, very complicated and soft elements of the male song, which are typically repeated at intervals of several to many minutes. After hearing the response, the male drastically changes its song by producing only the soft elements. These parts of the song contain syllables with a unique spectral composition and others that may threaten eavesdropping rivals. In this species both sexes probably move towards each other during mate localization. At present, we can only speculate about the adaptive nature of the different strategies. [ABSTRACT FROM AUTHOR]