Involvement of Mechanosensory Complex Structures of the Cricket <Emphasis Type="Italic">Gryllus bimaculatus</Emphasis> Larvae (Orthoptera,Gryllidae) in Triggering of Motor Responses to Sound

Using an ethological approach, we studied the possibility of sound perception as well as probable contribution of diverse mechanosensory systems composing the mechanosensory complex to triggering of motor responses to sound stimulation in the cricket Gryllus bimaculatus larvae. It was shown that larvae can perceive sounds and respond to them by a locomotor reaction in a relatively broad frequency range, which becomes narrower as sound intensity decreases [0.1–6.6 kHz (111 ± 3 dB SPL), 0.1–1.4 kHz (101 ± 3 dB SPL), 0.1–0.8 kHz (91 ± 3 dB SPL]. Sound perception and triggering of motor responses appear to involve the cercal organs (CO), subgenual organs (SO) and, probably, other distant mechanosensory organs (DMO). Normal functioning of CO is essential for triggering locomotor responses to sound within the ranges of 1–1.4 kHz (101 ± 3 dB SPL) and 0.1–0.8 kHz (91 ± 3 dB SPL). CO are not necessary for triggering of motor responses to cues with an intensity of 111 ± 3 dB. SO and, probably, other DMO provide locomotor responses to sound within the ranges of 0.1–6.6 kHz (111 ± 3 dB SPL), 0.1–0.9 kHz (101 ± 3 dB SPL), and 0.1–0.3 kHz (91 ± 3 dB SPL). Thus, last instar larvae of G. bimaculatus lacking the tympanal organs can perceive sounds using CO, SO and, probably, other DMO, which (as in cricket imagoes) are likely to compose an integrated mechanosensory complex providing adequate acoustic behavior of this cricket species. Performance efficiency and sensitivity of the mechanosensory complex (specifically, CO) rely on the thoroughness of grooming. After self-cleaning of CO, the level of larval motor activity in response to cue presentation returned to the baseline and sometimes even increased. We assume that under normal conditions the mechanosensory complex, which triggers motor responses to a sound, is involved in the defensive escape response aimed at rescuing from predators.     

Basic elements of behavior of the cricket <Emphasis Type="Italic">Phaeophilacris bredoides</Emphasis> Kaltenbach (Orthoptera,Gryllidae)

The intraspecific behavior of the non-singing cricket Phaeophilacris bredoides Kaltenbach, 1986, which has no tympanal system, stridulatory apparatus, and classical acoustic communication, was studied. Even though this cricket has no song, its intraspecific behavior can be differentiated into reproductive and agonistic (defensive and aggressive), as this was done before for singing crickets. The main elements and the sequence of the phases were described for reproductive behavior. The active role during copulation belongs to the male. Wingflicks and rocking movements of the male can function as a “song.” Wing-flicks apparently generate air movements that function as short-range signals during reproductive and aggressive behavior. Substrate-borne vibrations produced by rocking also seem to be associated with aggressive behavior. Antennal contacts form an important part of interaction between crickets of both sexes. Thus, intraspecific signaling is at least partly mediated by mechanosensory channels. The assumption about the possible direction of evolution in the singing and non-singing groups of crickets was made.     

Involvement of the mechanosensory complex structures of the cricket <Emphasis Type="Italic">Phaeophilacris bredoides</Emphasis> in triggering of motor responses to sound

Using an ethological approach, we studied the possibility of sound perception as well as probable contribution of diverse mechanosensory systems composing the mechanosensory complex to triggering of motor responses to sound stimulation in imaginal crickets Phaeophilacris bredoides lacking the tympanal organs (“deaf”). It was shown that Ph. bredoides imagoes are able to perceive sounds and respond to sound cues by a locomotor reaction in a relatively broad frequency range which becomes narrower as sound intensity decreases [0.1–6.0 kHz (111 ± 3 dB SPL), 0.1–1.5 kHz (101 ± 3 dB SPL), 0.1–1.3 kHz (91 ± 3 dB SPL), 0.1–0.6 kHz (81 ± 3 dB SPL), and 0.1 kHz (71 ± 3 dB SPL)]. Sound perception and triggering ofmotor responses appear to involve the cercal organs (CO), subgenual organs (SO) and, probably, other distant mechanosensory organs (DMO). CO are essential for triggering of locomotor responses to sound within the ranges of 1.6–6.0 kHz (111 ± 3 dB SPL), 1–1.5 kHz (101 ± 3 dB SPL), 0.9–1.3 kHz (91 ± 3 dB SPL), and 0.5–0.6 kHz (81 ± 3 dB SPL). SO and, probably, other DMO provide locomotor responses to sound within the ranges of 0.1–6.0 kHz (111 ± 3 dB SPL), 0.1–0.8 kHz (101 ± 3 dB SPL), 0.1–0.4 kHz (91 ± 3 dB SPL), and 0.1–0.4 kHz (81 ± 3 dB SPL). From this, it follows that “deaf” (nonsinging) Ph. bredoides can perceive sounds using CO, SO and, probably, other DMO, which (as in singing crickets) are likely to compose an integrated mechanosensory complex providing adequate acoustic behavior of this cricket species. Performance efficiency and sensitivity of the mechanosensory complex (specifically, of CO) rely on the thoroughness of grooming. Following self-cleaning of CO, the level of cricket motor activity in response to cue presentation returned to the baseline and sometimes even increased. Whether or not crickets of this species communicate acoustically is yet to be found out, however, we suggest that the mechanosensory complex, which triggers motor responses to a sound, is normally involved in the defensive escape response aimed at rescuing from predators.     

Erratum to: The original online version of the following articles was revised: the issue date is not January 2020, but January 2021

Journal of Evolutionary Biochemistry and Physiology - A Correction to this paper has been published: https://doi.org/10.1134/S0022093021020216     

Ontogeny of the cricket Phaeophilacris bredoides Kaltenbach (Orthoptera, Gryllidae)

Development of Phaeophilacris bredoides Kalt. was studied under stable laboratory conditions: temperature of 26°C, air humidity 60%, and 12L: 12D photoperiod (Knyazev, 1985). The life cycle of Ph. bredoides includes four stages: egg, pronymph, nymph, and adult. The duration of embryonic development is 28 days. The nymphal ontogeny lasts 230 days and consists of 25 instars. The duration of nymphal instars (days) is: 1st—16, 2nd—6, 3rd—8, 4th—10, 5th—10, 6th—15, 7th—10, 8th—8, 9th—9, 10th—11, 11th—11, 12th—8, 13th—9, 14th—10, 15th—7, 16th—9, 17th—7, 18th—7, 19th—7, 20th—10, 21st—11, 22nd—7, 23rd—9, 24th—6, and 25th—9. The duration of adult life is 126 days in males and 125 days in females. Three periods were distinguished in the imaginal ontogeny of males and females: pre-reproductive, reproductive, and post-reproductive. The pre-reproductive period begins with the molt to the adult and ends with the onset of reproductive behavior in males and with the first copulation in females. Its duration is 4 (3–6) days in males and 5 (2–7) days in females. The reproductive period in males starts with the onset of reproductive behavior on the 4th (3rd–6th) day and lasts 119 (98–135) days. In females it begins when they start responding to males’ courtship behavior and lasts 116 (97–133) days. The female reproductive period includes two alternating phases: copulation and egg-laying. The egg-laying phase is initiated by successful copulation. The post-reproductive period in females starts when oviposition ceases and in males, when their reproductive behavior disappears. This period lasts about 3 (2–3) days in males and 4 (2–7) days in females, until the insect dies.