Xenogryllus mozambicus Robillard

Jaiswara, Ranjana, Dong, Jiajia, Ma, Libin, Yin, Haisheng & Robillard, Tony, 2019, Taxonomic revision of the genus Xenogryllus Bolívar, 1890 (Orthoptera, Gryllidae, Eneopterinae, Xenogryllini), Zootaxa 4545 (3), pp. 301-338: 328-331

publication ID

https://doi.org/10.11646/zootaxa.4545.3.1

publication LSID

lsid:zoobank.org:pub:A6A7B9CE-9905-4DA7-8011-747D4B9325F7

persistent identifier

http://treatment.plazi.org/id/6A6AC46E-CE1E-FFEB-E9AB-FDC2FEAAFD83

treatment provided by

Plazi

scientific name

Xenogryllus mozambicus Robillard
status

n. sp.

Xenogryllus mozambicus Robillard  n. sp.

( Figs 2View FIGURE 2 A–D, 3K–L, 4H, 5F, 7J–K, 8F, 9D, 11H–J, 12C, 15, 16)

Xenogryllus eniopteroides  (wrong spelling of X. eneopteroides  )—Toms 1984: 309.

Type material. Holotype, ♂, Mozambique: Cabo Delgado, Pantanos de Nhica, zone herbacée à l’Est du camp [herbaceous area E of camp], 10°45’19,1"S 40°13’00"E, 122 m, 29.xi.2009, T. Robillard, nuit, enregistrement appel [call recording MNHN-SO-2018-140] (TR475) (MNHN-EO-ENSIF1517)GoogleMaps  . Allotype, ♀, Mozambique: Cabo Delgado, mare SE de Nhica, bras mort de la Rovuma [pond SE Nhica, dead arm of Rovuma river ], 10°45’41,9"S 40°13’31,7"E, 124 m, 27.xi.2009, T. Robillard, mort en élevage [dead in captivity] (MNHN-EO- ENSIF1539)GoogleMaps  . Paratypes (8♂, 4♀): Mozambique: Cabo Delgado, same information as holotype: 1♂, 1♀, morts en élevage [dead in captivity] (MNHN-EO-ENSIF1576-ENSIF1556). Same information as allotype: 2♂, mort en élevage [dead in captivity] (MNHN-EO- ENSIF1557, ENSIF1508). Mare SE de Nhica, bras mort de la Rovuma [pond SE Nhica, dead arm of Rovuma river], 10°45’41,9"S 40°13’31,7"E, 124 m, nuit, zone herbacée en bord de piste [herbaceous area near track] T. Robillard: 22.xi.2009, 1♂ (MNHN-EO-ENSIF1554), 3♀ (MNHN-EO- ENSIF1502, ENSIF1503, ENSIF1505); 23.xi.2009, 1♂ (TR208), enregistrement appel Take 224 [call recording MNHN-SO-2018-133] (MNHN-EO-ENSIF3079); 1♂ (TR206), enregistrement appel Take 222 [call recording MNHN-SO-2018-134], molecular sample X7 - XenMoz (MNHN-EO-ENSIF1515). Mare SW de Nhica, bras mort de la Rovuma [pond SW Nhica, dead arm of Rovuma river], 10°52’09,5"S 40°06’47,1"E, 122 m, 24.xi.2009, nuit, zone herbacée en bord de piste [herbaceous area near track] T. Robillard: 1♂ (TR224), hautes herbes (h=1.3 m) [on high grass], enregistrement appel Take 228 [call recording MNHN-SO-2018-135], molecular sample X23 (MNHN-EO-ENSIF1559); 1♂, mort en élevage (MNHN-EO-ENSIF1581)GoogleMaps  .

Additional material examined. Mozambique: Delagoa   [Maputo Bay], xii.1898, 1 ♂, identified Phormincter  species nova by A. Finot (MNHN). South Africa: Zululand, Mtunzini , 8.i.1952, R. Toms, 1♂, R146, identified Xenogryllus eneopteroides  by B. C. Townsend, 1984, B.M.1983-166 ( NHMUK 010926568)  . Malawi: Fish Eagle Bay Lodge, herbaceous area near lake Malawi ( Mal 7), S13°02'21.1" E34°19'34.8", 503 m, 6.x.2018, night, 2♂, call recording, 1♀, T. Robillard, K. Salazar & R. Murphy ( MNHN)GoogleMaps  .

Type locality. Mozambique, Cabo Delgado, Pantanos of Nhica , 10°45’19,1"S 40°13’00"EGoogleMaps  .

Distribution. Mozambique, South Africa, Malawi.

Etymology. Species named after the type locality.

Diagnosis. Species of average to large size, close to X. eneopteroides  and X. maniema  n. sp. From X. eneopteroides  , the new species differs by rather larger size, face more rounded, almost globular in lateral view, absence of T-shaped median band on pronotum (also absent in X. maniema  ), larger mirror, and slight differences in male genitalia. From X. maniema  n. sp., X. mozambicus  mostly differs by male genitalia with larger lophi ( Fig. 8FView FIGURE 8) and presence of transverse carina on ventral face of lophi (also present in X. eneopteroides  ). As X. maniema  and X. eneopteroides  , X. mozambicus  differs from X. lamottei  n. sp. and Asian species by strongly carinated lateral angles of pronotum.

Description. Species of average size ( Fig. 2View FIGURE 2 A–D), coloration light brown little contrasted. Eyes little prominent laterally ( Fig. 3KView FIGURE 3), higher than long, occupying almost half of head height in lateral view. Face globular in lateral view ( Fig. 3LView FIGURE 3), with typical whitish mask underlined by a black line below eyes and on mandibles. Pronotum dorsal disc strongly carinated laterally, coloration light brown, with a median dark brown band, not extended laterally near anterior margin; lateral lobes almost homogeneously dark brown. First article of antennae dark brown.

Male. FWs very wide, longer than abdomen; dark coloration anterior to 1A including angle of 1A ( Fig. 5FView FIGURE 5). Stridulatory file with 505 teeth (n=1) on transverse part of 1A. FW venation as in X. eneopteroides  , mirror wider and apical field longer, forming a long triangle including 5–6 (n=8) cell alignments.

Male genitalia ( Fig. 7View FIGURE 7 J–K): Similar to X. eneopteroides  , except longer pseudepiphallic lophi ( Fig 8FView FIGURE 8); transverse carina on ventral face of lophi present but weak.

Female ( Fig. 2View FIGURE 2 C–D) FW dorsal field elongate, with 8–9 longitudinal veins (m = 9, n = 6). Subgenital plate with a shallow apical indentation ( Fig. 9DView FIGURE 9). Ovipositor short, about 0.6 times FIII length.

Female genitalia: Copulatory papilla ( Fig. 11View FIGURE 11 H–J) as in X. eneopteroides  , conical and narrow, well-sclerotized except base and apex.

Life history traits. X. mozambicus  lives in areas of wet savannah ( Fig. 15View FIGURE 15) or on the edge ponds and lakes. Individuals of both sexes are found only at night in herbaceous vegetation, and males sing at night from the vegetation (ca. 30–80 cm high). Toms (1984) demonstrated that this species has directional calls and turs while calling, giving rise to changes in sound intensity.

Calling song ( Figs 12CView FIGURE 12, 16View FIGURE 16). At 21.5 °C, males of X. mozambicus  emit almost continuously long bouts of highly musical calling songs. After a warming phase, call bouts are made of successions of echemes of 23 ± 2 syllables, barely separated from each other (echeme duration = 3.13 ± 0.29 s; echeme period 3.21 ± 0.30 s, echeme duty cycle = 97.6 %), with a regular amplitude profile, except for the last syllable, which is more intense. Within echemes, syllables are initially organized in 4 ± 1 doublets, which are followed by a series of similar syllables. Syllables are very long (syllable duration = 126 ± 5 ms), with a relatively short syllable period of 137 ± 8 ms (syllable duty cycle = 92%). All syllables are characterized by a large amplitude modulation: in initial doublets within echemes, the first syllables are less intense than the second ones and they start with a lower amplitude than their end (initial amplitude <ending amplitude), contrary to the second syllables of the doublets (initial amplitude> ending amplitude); the rest of the syllables have a higher starting amplitude, except for the last syllable of each echeme, which has a higher ending amplitude. The frequency spectrum shows a pure-tone dominant frequency at 3.3 ± 0.01 kHz, followed by a rich harmonic content including three powerful harmonics at ca. 6.6, 9.9, 13.2 kHz, especially visible in ending syllables.

Measurements. See Table 7.

Taxonomic discussion. The specimens observed by Toms (1984) and identified Xenogryllus eniopteroides  (wrong spelling for X. eneopteroides  ) from Zululand (Mtunzini and Eastern Transvaal (Clanor)), South Africa, belong to X. mozambicus  n. sp. according to one male specimen observed from the series of Toms (NHMUK 010926568).

MNHN

Museum National d'Histoire Naturelle