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BioAcoustica is a free, open repository of wildlife sound recordings from the Natural History Museum, London.

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Tettigonia viridissima

Species · 25 recordings · 8 specimens

Recordings

579:28 Tettigonia viridissima (794r10) 16-Nov1:28 · W. J. Reynolds
597:7 Tettigonia viridissima (003r5)22:03 · David R. Ragge
600:4 Tettigonia viridissima (15r1)16:07 · David R. Ragge
600:5 Tettigonia viridissima (15r2)8:53 · David R. Ragge
896:6 Tettigonia viridissima (61r1)2:34 · G. F. Wade
897:2 Tettigonia viridissima (63)6:00 · David R. Ragge; J. F. Burton; G. F. Wade
134_7_Tettigonia viridissima5:00 · David R. Ragge
565_6_Tettigonia viridissima1:06
565_7_Tettigonia viridissima0:28
26 Great Green Bush-cricket0:36
Tettigonia viridissima 868_20:59 · P Rudkin
Tettigonia viridissima0:34
Tettigonia viridissima0:29
Tettigonia viridissima0:34
565_8 Tettigonia viridissima0:31
male from Poznan, Poland0:07
field recording at 21.50 h, ca. 16°C (Uher, tape no. U3)0:20
field recording, 8/8/1989, 18°C (Sony WM-D3 with Universum mono, tape: UX-ES90, tape no. YU2/89:491-525)0:36
394:5 Tettigonia viridissima(360r2)2:53 · W. J. Reynolds
394:6 Tettigonia viridissima(360r2b)3:50 · W. J. Reynolds
394:7 Tettigonia viridissima(361)3:51 · W. J. Reynolds; David R. Ragge
399:9 Tettigonia viridissima(412)3:53 · W. J. Reynolds
399:10 Tettigonia viridissima(412b)1:50 · W. J. Reynolds
399:11 Tettigonia viridissima(412c)0:45 · W. J. Reynolds
562:15 Tettigonia viridissima (760r1)1:13 · W. J. Reynolds

Specimens

Tettigonia viridissima BioAcoustica Rudkin 21998-06-21 · P Rudkin
Tettigonia viridissima NHMUK BMNH(E) 010210772GB · 1976-07-26 · B. C. Townsend
Tettigonia viridissima NHMUK BMNH(E) 010210771FR · 1974-08-24 · David R. Ragge
Tettigonia viridissima NHMUK BMNH(E) 010210927
Tettigonia viridissima NHMUK BMNH(E) 010210928
Tettigonia viridissima NHMUK BMNH(E) 010210929
Tettigonia viridissima NHMUK BMNH(E) 010210930
Tettigonia viridissima NHMUK BMNH(E) 010211042

Literature

Grzywacz, Beata; Heller, Klaus-Gerhard; Warchałowska-Śliwa, Elżbieta; Karamysheva, Tatyana V.; Chobanov, Dragan Petrov (2017). Evolution and systematics of Green Bush-crickets (Orthoptera: Tettigoniidae: Tettigonia) in the Western Palaearctic: testing concordance between molecular, acoustic, and morphological data. Organisms Diversity & Evolution, 17(1): 213 - 228.
Montealegre-Zapata, Fernando; Ogden, Jessica; Jonsson, Thorin; Soulsbury, Carl D. (2017). Morphological determinants of carrier frequency signal in katydids (Orthoptera): a comparative analysis using biophysical evidence. Journal of Evolutionary Biology.
Jeliazkov, Alienor; Bas, Yves; Kerbiriou, Christian; Julien, Jean-François; Penone, Caterina; Le Viol, Isabelle (2016). Large-scale semi-automated acoustic monitoring allows to detect temporal decline of bush-crickets. Global Ecology and Conservation, 6: 208 - 218.
Grzywacz, Beata; Heller, Klaus-Gerhard; Lehmann, Arne W.; Warchałowska-Śliwa, Elżbieta; Lehmann, Gerlind U.C. (2014). Chromosomal diversification in the flightless Western Mediterranean bushcricket genus Odontura (Orthoptera: Tettigoniidae: Phaneropterinae) inferred from molecular data. Journal of Zoological Systematics and Evolutionary Research, 52(2): 109 - 118.
Hartbauer, Manfred; Ofner, Elisabeth; Grossauer, Viktoria; Siemers, Björn M. (2010). The Cercal Organ May Provide Singing Tettigoniids a Backup Sensory System for the Detection of Eavesdropping Bats.
Bangert, Marc; Kalmring, Klaus; Sickmann, Thomas; Stephen, Richard; Jatho, Martin; Lakes-Harlan, Reinhard (1998). Stimulus transmission in the auditory receptor organs of the foreleg of bushcrickets (Tettigoniidae) I. The role of the tympana.
Arak, Anthony; Eiriksson, Thorleifur; Radesäter, Tommy (1990). The adaptive significance of acoustic spacing in male bushcrickets Tettigonia viridissima: a perturbation experiment. Behavioral Ecology and Sociobiology, 26(1).
Ahlén, Ingemar (1981). Ultraljud hos svenska vårtbitare. Entomologisk Tidskrift, 102: 27-41.
Autrum, H. (1960). Phasische und tonische antworten vom tympanalorgan of Tettigonia viridissima. Acoustica, 10: 339-348.

Behaviour

The great green bush-cricket is nocturnal, but the males often sing from mid-afternoon onwards. The song is one of the loudest emitted by any British orthopteran, and cen be heard at distances of several meters (Ragge, 1965, says 200 metres, but this is presumably for those with better hearing than mine!). The tone is slightly metallic and rasping, and is produced in continuous, prolonged bursts. When singing the male appears to 'pump' his abdomen rhythmically - presumably to anhance respiration. Even when singing the crypti ccoloration of a male perched among vegetation makes it very difficult to locate. There is some competition between males for song perches, and where the population is dense one may nip an intruder with his mandibles. The latter will usually dive down into lower vegetation.

Source: Benton, Ted (2012). Grashoppers & Crickets. HarperCollins, 120.

Behaviour

The loud calling song, produced mainly in the late afternoon and after dark, consists of sequences of closely spaced disyllabic echemes. The echeme repetition rate depends on temperature: 10-15/s is common, but in high daytime tempertaures the rate may increase to 20/s and on cool nights may be as low as 5/s. Typically the echeme sequences are interrupted at irregular intervals by very short pauses (Figs 188-190), usually of less than a second and sometimes, at high temperatures, as short as 0.2-0.3 s. Occasionally, long echeme-sequences are produced without even the briefest interruption (Figs 191, 192); the longest uninterrupted sequence we have recorded lasted 3 minutes 9 seconds. Oscillographic analysis shows that nearly all the sound is produced by the closing strokes of the fore wings, although quiet opening hemisyllables are sometimes present. The duration of the two closing hemisyllables comprising each echeme again depends on temperature: 15-25 ms for each hemisyllable is common, but in hot conditions they may last 10 ms or even less and on cool nights tehy may be as long as 50 ms. The second hemisyllable in each echeme is often slightly longer tahn the first. The gap between the two hemisyllables varies from about 6 ms (warm conditions) to about 35 ms (cool conditions), and the interval between successive echemes varies from about 20 ms to about 100 ms, again depending on temperature. Each closing hemisyllable is typically broken up into a very variable number of discrete pulses of sound separated by gaps of varying duration but usually of theorder of 1 ms. There are sometimes fewer than 10 of these pulses in one hemisyllable (see for example Fig. 204) and so, in such cases, they are unlikely to represent individual tooth-impacts.

Source: Ragge, D. R.; Reynolds, W. J. (1998). The Songs of the Grasshoppers and Crickets of Western Europe. Harley Books.

Behaviour

The song is a loud buzzing audible from about 50m. As two syllables are coupled into a double sound, the song - in contrast to T. cantans - is always clearly cut up into 'pulses' of sound.

Source: Bellman, Heiko (1988). A Field Guide to the Grasshoppers and Crickets of Britain and Northern Europe. William Collins & Sons.

Behaviour

Lehtohepokatilla on kovaäänien kutsulaulu, joka voi kuulua jopa yli sadan metrin päähän. Laji aloittaa laulunsa yleensä iltapäivälla, ja mikäli lämpötila on riittävä, laulu on kiihkeimmillään illalla ja se jatkuu heikentyneenä aamuun asti. Sirittääkseen lehtohepokatti vaattii noin kymmenen asteen tai heiman korkeamman lämpötilan. Kutsulaulu jatkuu lämpimällä ilmalla pitkään ilman taukoja (CD2, CD3), mutta lämpötilan laskiessa se muuttuu katkonaiseksi (CD27). Soiton alkaessa iltapäivällä tai lämpimänä päivänä jo aamupäivän puolella se on aluksi katkonaista. Äänen voimakkuuden huippu on noin 10 kHz:n taajuudessa (kuva s. 34).

Source: Karjalainen, Sami (2009). Suomen heinäsirkat ja hepokatit.

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