Species
What the sources say about this taxon, as written.
behaviour · bio.acousti.ca
(1 male recorded) We successfully recorded the singing of one specimen at 28°C. This male's duty cycle was extremely low: in making a succession of seven call he sang for about 1/3 of 1% of the time available. Each call was a zip lasting 106.7 ms (c.v. = 1.6%). One complete zip is shown in Fig. 31 A. Average down time between calls was 35.8 s (n=9). The amplitude modulation of the call is complex and a little variable; it incorporates trains of rapid-decay pulses of low amplitude as well as trains of higher amplitude prolonged pulses (Fig. 31B); within the trains these latter tend to increment in duration. The maximum prolonged pulse duration achieved was in the final train (Fig. 31B,C): 2.1 ms. The call always begins with a pair of low-amplitude rapid-decay pulse pulse trains. Then there are a few short sinusoidal pulses at higher amplitude and finally a short succession of the rather variable (presumed) phonatomes, each comprised of a minor low amplitude train preceding a major train of several maximally sustained pure tone pulses (Fig. 31 A,B). Though this insect's song includes so many low amplitude rapid-decay pulse trains, its spectrum is is nevertheless dominated by a single relatively high-Q peak of unusual symmetry (Fig. 31 D,E). At any signficant distance from a singer a female would only perceive this dominant carrier. The peak is the product of the higher intensity pulses which involve one dominant frequency: 29.3 kHz (c.v1.3%). Though not obvious in all spectra there are also very low harmonic peaks. There is a fundamental at 14.5 kHz >37 dB down. The principal carrier is thus the first harmonic of this suppressed fundamental. Other low harmonic peaks occur, 2'nd, 3'rd, 5th, all >30 dB below the dominant peak. One prolonged pulse is shown (Fig. 31C) at a resolution that reveals the pure-tone sinusoid; the power spectrum of this particular time sample is shown in Fig. 31 E.
6 measurements across 6 traits. Each name links to its term in the audioBlast vocabulary.
Every value behind the summaries above. Each links to its own record in the API, which carries the reference it was taken from.
| Trait | Value | Call | Part | Sex | Temp. | Source |
|---|---|---|---|---|---|---|
| Fundamental Frequency | 14.5 | Calling Call | Male | bio.acousti.ca | ||
| Duty Cycle (%) | 0.33 | Calling Call | Male | bio.acousti.ca | ||
| Length Of Stridulatory File | 1.64 | Male | bio.acousti.ca | |||
| Peak Frequency (kHz) | 29.3 | Calling Call | Male | bio.acousti.ca | ||
| Number Of Teeth On Stridulatory File | 142 | Male | bio.acousti.ca | |||
| Centre Frequency (kHz) | 22.30 | Calling Call | Male | bio.acousti.ca |
Counts are recordings at or below each taxon, so an empty branch shows as empty before you click it. A dash means the join view holds no column for that rank and cannot roll up to it.
Publications audioBlast links to this taxon.
The rows audioBlast holds for this taxon, each matched to the same Catalogue of Life node. Where a source classifies it differently, its own classification is kept.
| Source | Its name | Its rank | Its family | Record |
|---|---|---|---|---|
| bio.acousti.ca | Triencentrus atrosignatus | Species | Tettigoniidae | bio.acousti.ca/5258 |
Bioschemas is in the head of this page. The Darwin Core RDF lives at the API address below, which negotiates JSON-LD and Turtle.
{
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"@id": "https://browse.acousti.cloud/taxon/triencentrus-atrosignatus/",
"name": "Triencentrus atrosignatus",
"taxonRank": "species",
"url": "https://browse.acousti.cloud/taxon/triencentrus-atrosignatus/",
"sameAs": "https://api.audioblast.org/taxon/CoL/58PC3",
"parentTaxon": {
"@type": "Taxon",
"name": "Triencentrus",
"taxonRank": "genus",
"url": "https://browse.acousti.cloud/taxon/triencentrus/"
}
}