ABSTRACT
Pair formation in the bladder grasshopper (Bullacris membracioides) is by duetting and male phonotaxis. Low-frequency stridulatory signals are emitted by an abdominal resonator in the male and are answered by females using a species-specific time delay. Acoustic transmission in the natural environment was studied using playback of sexual signals over distances of 450m under two atmospheric conditions (day and night). Upward-refracting sound conditions and a sound shadow zone beyond approximately 50m prevailed during the day. Acoustic enhancement was demonstrated at night when downward-refracting temperature inversions created a tunnel effect with sound caught between the ground and zones of different temperatures. Transmission conditions are almost ideal at night when the species actually calls; calling distances of 150m for the male signal in the afternoon increased to 1.5-1.9km at night, arguably the largest calling distance yet reported for insects. In contrast, female calls transmit over a maximum of 50m, signifying a marked discrepancy in the active space of sex-specific signals. Transmission distance may, however, be profoundly affected by levels of masking noise. Adaptations to increase the signal range may variously be found in the signal itself, in behaviour patterns or in the sensory system. Here we demonstrate aspects of the first two types of adaptation in the sexual signalling system of a grasshopper in which maximizing the calling range appears to be the major selection pressure, with lesser effects imposed by inter- and intraspecific pressures and by the transmission channel.
Subject(s)
Grasshoppers/physiology , Sexual Behavior, Animal , Animals , Female , MaleABSTRACT
The species assemblages of cichlids in the three largest African Great Lakes are among the richest concentrations of vertebrate species on earth. The faunas are broadly similar in terms of trophic diversity, species richness, rates of endemism, and taxonomic composition, yet they are historically independent of each other. Hence, they offer a true and unique evolutionary experiment to test hypotheses concerning the mutual dependencies of ecology and brain morphology. We examined the brains of 189 species of cichlids from the three large lakes: Victoria, Tanganyika, and Malawi. A first paper demonstrated that patterns of evolutionary change in cichlid brain morphology are similar across taxonomic boundaries as well as across the three lakes [van Staaden et al., 1995 ZACS 98: 165-178]. Here we report a close relationship between the relative sizes of various brain structures and variables related to the utilization of habitat and prey. Causality is difficult to assign in this context, nonetheless, prey size and agility, turbidity levels, depth, and substrate complexity are all highly predictive of variation in brain structure. Areas associated with primary sensory functions such as vision and taste relate significantly to differences in feeding habits. Turbidity and depth are closely associated with differences in eye size, and large eyes are associated with species that pick plankton from the water column. Piscivorous taxa and others that utilize motile prey are characterized by a well developed optic tectum and a large cerebellum compared to species that prey on molluscs or plants. Structures relating to taste are well developed in species feeding on benthos over muddy or sandy substrates. The data militated against the existence of compensatory changes in brain structure. Thus enhanced development of a particular function is generally not accompanied by a parallel reduction of structures related to other modalities. Although genetic and environmental influences during ontogeny of the brain cannot be isolated, this study provides a rich source of hypotheses concerning the way the nervous system functions under various environmental conditions and how it has responded to natural selection.
