02072nas a2200205 4500008004100000245008700041210006900128520133100197653001601528653002001544653002201564653001901586653002901605653001801634100002101652700002101673700002001694700002101714856013101735 2014 eng d00aProcessing of simple and complex acoustic signals in a tonotopically organized ear0 aProcessing of simple and complex acoustic signals in a tonotopic3 a

Processing of complex signals in the hearing organ remains poorly understood. This paper aims to contribute to this topic by presenting investigations on the mechanical and neuronal response of the hearing organ of the tropical bushcricket species Mecopoda elongata to simple pure tone signals as well as to the conspecific song as a complex acoustic signal. The high-frequency hearing organ of bushcrickets, the crista acustica (CA), is tonotopically tuned to frequencies between about 4 and 70 kHz. Laser Doppler vibrometer measurements revealed a strong and dominant low-frequency-induced motion of the CA when stimulated with either pure tone or complex stimuli. Consequently, the high-frequency distal area of the CA is more strongly deflected by low-frequency-induced waves than by high-frequency-induced waves. This low-frequency dominance will have strong effects on the processing of complex signals. Therefore, we additionally studied the neuronal response of the CA to native and frequency-manipulated chirps. Again, we found a dominant influence of low-frequency components within the conspecific song, indicating that the mechanical vibration pattern highly determines the neuronal response of the sensory cells. Thus, we conclude that the encoding of communication signals is modulated by ear mechanics.

10abushcricket10acrista acustica10aElectrophysiology10ainsect hearing10alaser Doppler vibrometry10aTettigoniidae1 aHummel, Jennifer1 aWolf, Konstantin1 aKössl, Manfred1 aNowotny, Manuela uhttps://royalsocietypublishing.org/doi/10.1098/rspb.2014.1872https://royalsocietypublishing.org/doi/pdf/10.1098/rspb.2014.187202330nas a2200229 4500008004100000022001400041245008500055210006900140260001300209300001100222490000700233520169200240653001201932653002201944653001201966653001201978653002701990653001002017100001802027700001402045856004102059 1966 eng d a0022-094900aThe neuromuscular mechanism of stridulation in crickets (Orthoptera: Gryllidae).0 aneuromuscular mechanism of stridulation in crickets Orthoptera G c1966 Aug a151-640 v453 a

Study of the insect neuromuscular system appears very promising as a means of
explaining behaviour in terms of cellular operation. The relatively small number of
neurons, the ganglionic nature of the nervous system, the simplicity of the neuro-
muscular arrangement, and the repetitiveness of behavioural sequences all lend them-
selves to a solution of this problem. As a result, an increasing number of investigators
have been turning their attention to insects and especially to the large orthopterans.
Recently, Ewing & Hoyle (1965) and Huber (1965) reported on muscle activity
underlying sound production in crickets. The acoustic behaviour is well understood
(Alexander, 1961) and in the genera Gryllus, Acheta and Gryllodes communication is
mediated by three basic songs composed of three types of pulses. While working
independently on this system at the University of Cologne (W.K.) and the University
of Michigan (D.B.) using various Gryllus species, we found a number of basic
differences between the muscle activity in our crickets and that reported by Ewing
& Hoyle (1965) for Acheta domesticus. These two genera, Gryllus and Acheta, are so
nearly identical that they are distinguished solely by differences in the male genitalia
(Chopard, 1961). The present paper constitutes a survey of muscle activity patterns
producing stridulation in four species of field crickets. Since the work of the two
authors was carried out independently, non-overlapping experiments will be initialled
to indicate the investigator.

10aAnimals10aElectrophysiology10ainsects10amuscles10aneuromuscular junction10asound1 aBentley, D, R1 aKutsch, W uhttps://bio.acousti.ca/es/node/17213