Genus
What the sources say about this taxon, as written.
discussion ·
Plazi
Remarks. Our single male specimen ( Fig. 1A ) belongs to the subgenus Bejorama Otte, 1988 on the basis of the distinct stridulatory apparatus ( Fig. 1B ), presence of strong setae along posterior edge of male anal plate ( Fig. 1C ), and lack of distinct transverse fold and dorsal denticle on epiphallus ( Fig. 2 ). It has similar male genitalia and tegminal venation to that of Duolandrevus luzonensis Otte, 1988 from Luzon Island, Philippines as illustrated in Otte (1988) . While this may indicate a new locality record for the Filipino species, there are however still some slight differences: our male specimen has a reduced anal area of the tegmen and with mirror much broader than long ( Fig. 1B vs. Fig. 1E ); posterolateral epiphallic lobe more slender (when viewed dorsally and laterally) and with ventral process more elongated ( Fig. 2 ). Owing to the lack of further information, we tentatively identify the specimen to be close to D. luzonensis .
key ·
Plazi
1. Fore tibia usually with two tympana, but sometimes this tibia with one tympanum. Male tegmina with developed stridulatory apparatus............................................................................................ 2 - Fore tibiae without tympana. Male tegmina with only traces of stridulatory apparatus (this apparatus almost lost). [Sumatra]............................................................................. Surdolandrevus Gorochov, 2003 2. Head distinctly depressed dorsoventrally, with more or less angular rostral projection in profile. Hind tibia with articulated dorsal spines moderately long and unarticulated dorsal spines short, denticle-like...................................... 3 - Head slightly depressed or almost not depressed dorsoventrally, with rounded rostral projection in profile. Hind tibia with all dorsal spines more or less long. [Sumatra]......................................... Spinolandrevus Gorochov, 1999 3. Male genitalia with posterolateral epiphalluc lobes large and plate-like widened, or these lobes with numerous small denticles.................................................................................................... 4 - Male genitalia with posterolateral lobes not plate-like widened and lacking denticles................................ 5 4. Head moderately depressed dorsoventrally. Male genitalia with posterolateral epiphallic lobes rather small (not widened) and having numerous small denticles. [ Taiwan , Philippines , New Guinea , Lombok I.]..................... Jorama Otte, 1988 - Head strongly depressed dorsoventrally. Male genitalia with posterolateral lobes large and plate-like widened but lacking denticles. [New Guinea ].......................................................... Platylandrevus Gorochov, 2005 5. Male genitalia with epiphallus lacking distinct transverse fold or folds in middle part................................ 6 - Male genitalia with epiphallus having distinct transverse fold or a pair of lateral ones in middle part.................... 7 6. Male anal plate with dorsoapical denticle and / or with bundle of dense and rather strong setae in apical part. [Sumatra, Malacca , Sulawesi; possibly also Borneo, but all species described from Borneo unrevised in accordance to recent views]........................................................................................... Bejorama Otte, 1988 - Male anal plate without both dorsoapical denticle and distinct bundle of setae in apical part. [Java, Lombok I.]............................................................................................. Duolandrevus Kirby, 1906 7. Male tegmen with lateral field much shorter than dorsal field. [Central Vietnam ]............. Vietlandrevus Gorochov, 1996 - Male tegmen with lateral field not shorter or insignificantly shorter than dorsal field [from Japan and China to Northern Vietnam and Taiwan ; see also notes below]............................................. Eulandrevus Gorochov, 1988
2 measurements across 2 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 |
|---|---|---|---|---|---|---|
| Crepitation (Presence) | Absent | Male; Female | bio.acousti.ca | |||
| Sound Production Method | Elytral Stridulation | bio.acousti.ca |
50 in audioBlast.
38 more in the audioBlast browser.
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.
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 |
|---|---|---|---|---|
| Duolandrevus | Genus | Gryllidae | Plazi/Duolandrevus | |
| Duolandrevus | Genus | Gryllidae | iNaturalist/625420 | |
| Duolandrevus | Genus | — | xeno-canto/Duolandrevus | |
| bio.acousti.ca | Duolandrevus | Genus | Gryllidae | bio.acousti.ca/2610 |
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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