Ultrasonic songs and stridulum anatomy of Asiophlugis crystal predatory katydids (Tettigonioidea: Meconematinae: Phlugidini)

The behavioural ecology of ultrasonic-singing katydids is not well understood, and the general bioacoustics, barely known for a few Neotropical Meconematinae, tends to be overlooked for species from Southeast Asia. These include Asiatic species of Phlugidini, commonly known as crystal predatory katydids. One of its genera, Asiophlugis consists of 16 species for which acoustic signals and stridulum anatomy are broadly unknown. These characters can be used to understand species boundaries. Here, we sampled Asiophlugis from five sites in Malay Peninsula and Borneo Island, recorded the acoustic signals of five species plus one subspecies using ultrasound sensitive equipment, and examined their stridulum anatomy. The calling songs of the taxa involved were documented for the first time. We found that the stridulum anatomy (e.g., tooth distributions, tooth length and tooth density) is distinct between species, but less so between subspecies. In contrary, songs of different taxa are different based on acoustic parameters (e.g., pulse duration, peak frequency) and descriptive patterns, even between the subspecies. We also did not observe that song signals are more different in sympatry than in allopatry. Whether this can be generalised requires further sampling, highlighting the need for more research on the ultrasonic acoustic communication in Asiatic katydids

Shrinking wings for ultrasonic pitch production: hyperintense ultra-short-wavelength calls in a new genus of neotropical katydids (Orthoptera: tettigoniidae)

This article reports the discovery of a new genus and three species of predaceous katydid (Insecta: Orthoptera) from Colombia and Ecuador in which males produce the highest frequency ultrasonic calling songs so far recorded from an arthropod. Male katydids sing by rubbing their wings together to attract distant females. Their song frequencies usually range from audio (5 kHz) to low ultrasonic (30 kHz). However, males of Supersonus spp. call females at 115 kHz, 125 kHz, and 150 kHz. Exceeding the human hearing range (50 Hz–20 kHz) by an order of magnitude, these insects also emit their ultrasound at unusually elevated sound pressure levels (SPL). In all three species these calls exceed 110 dB SPL rms re 20 µPa (at 15 cm). Males of Supersonus spp. have unusually reduced forewings (<0.5 mm2). Only the right wing radiates appreciable sound, the left bears the file and does not show a particular resonance. In contrast to most katydids, males of Supersonus spp. position and move their wings during sound production so that the concave aspect of the right wing, underlain by the insect dorsum, forms a contained cavity with sharp resonance. The observed high SPL at extreme carrier frequencies can be explained by wing anatomy, a resonant cavity with a membrane, and cuticle deformation

Versatile Aggressive Mimicry of Cicadas by an Australian Predatory Katydid

Background: In aggressive mimicry, a predator or parasite imitates a signal of another species in order to exploit the recipient of the signal. Some of the most remarkable examples of aggressive mimicry involve exploitation of a complex signal-response system by an unrelated predator species. Methodology/Principal Findings: We have found that predatory Chlorobalius leucoviridis katydids (Orthoptera: Tettigoniidae) can attract male cicadas (Hemiptera: Cicadidae) by imitating the species-specific wing-flick replies of sexually receptive female cicadas. This aggressive mimicry is accomplished both acoustically, with tegminal clicks, and visually, with synchronized body jerks. Remarkably, the katydids respond effectively to a variety of complex, species-specific Cicadettini songs, including songs of many cicada species that the predator has never encountered. Conclusions/Significance: We propose that the versatility of aggressive mimicry in C. leucoviridis is accomplished by exploiting general design elements common to the songs of many acoustically signaling insects that use duets in pairformation. Consideration of the mechanism of versatile mimicry in C. leucoviridis may illuminate processes driving the evolution of insect acoustic signals, which play a central role in reproductive isolation of populations and the formation of species