Yoyetta delicata, Popple & Emery, 2022

Popple, Lindsay W. & Emery, David L., 2022, Five new species of Yoyetta Moulds (Hemiptera: Cicadidae: Cicadettinae) from south-eastern Australia, Zootaxa 5141 (5), pp. 401-441 : 421-427

publication ID

https://doi.org/ 10.11646/zootaxa.5141.5.1

publication LSID

lsid:zoobank.org:pub:CE3235D2-A4DA-4570-8CD8-5E05FFE7F952

DOI

https://doi.org/10.5281/zenodo.6598605

persistent identifier

https://treatment.plazi.org/id/B930879A-9E38-4141-FF57-FF3BA55FFDF6

treatment provided by

Plazi

scientific name

Yoyetta delicata
status

sp. nov.

Yoyetta delicata View in CoL n. sp.

( Plate 3 View PLATE 3 ; Figs 1 View FIGURE 1 , 2D View FIGURE 2 , 3D View FIGURE 3 , 4D View FIGURE 4 , 12–14 View FIGURE 12 View FIGURE 13 View FIGURE 14 )

Types. Holotype ♂, AUSTRALIA NSW, 4 km SSE of Stannum , 29.353249°S 151.803142°E, 4–7.i.2016, [permit no.] SL100704, L. W. Popple, 488-0005, K594160 ( AM). GoogleMaps

Paratypes. NEW SOUTH WALES. 1♀, same data as holotype, 488-0014, K594161 ( AM) GoogleMaps . 1♂, Armidale N.S.W., 19.xi.1966, C. W. Frazier, University of New England coll. Donated 1983 ; 1♀, same data as previous, N[ew] E[ngland] University , 6.xii.1966 ; 1♀, Dangar’s Falls , Armidale N.S.W., 16.xii.1962, C. W. Frazier, University of New England coll. Donated 1983 ; 7♂, 3♀, 5km W. of Torrington N.S.W., 10.i.1993, A. I. Knight; 2♂, 1♀, same data as previous, 18–22.xii.1990 ; 1♀ Upper Talbragar via Cassilis N.S.W., 26.xi.1963, T. G. Campbell ( ANIC) . 2♂, 1♀, same data as holotype, 488-0004, 488-0010, 488-0013 (DE) GoogleMaps . 1♂, Wetlands Place, Shortland , 32.876557°S 151.695962°E, 11.xii.2021, J. Poyitt ( JP) GoogleMaps . 6♂, 4♀, same data as holotype, 488-0002, 488-0003, 488- 0006 to 488-0009, 488-0011, 488-0012, 488-0015, 488-0016 GoogleMaps ; 1♂, Armidale , 12.xii.1958, K. L. Taylor, 487-0001 ( LWP) . 1♂, Mt Coryah, approx. 45 km NE. Narrabri , 25.xi.1981, 2500’, 25.xi.1981, G. & T. Williams, at light, in scler[ophyll] forest ; 1♂, Kanwal, near Wyong , 1.i.1972, G. Daniels ( MSM) . QUEENSLAND. 1♂, Daggs Falls via Killarney , 1.xi.2003, L. Popple, R. MacSloy, 488-0001 ( LWP) .

Audio records (LWP). NEW SOUTH WALES: 4 km SSE. of Stannum , 29.353249°S 151.803142°E, 4– 8.i.2016 GoogleMaps ; Bismuth Dam , 29°15’13’’S 151°38’20’’E, 6.i.2016 GoogleMaps . QUEENSLAND: 6 km west of Thane , 28°09’41’’S 151°37’59’’E, 11–12.xii.2001 GoogleMaps ; Queen Mary Falls , 28°20’30’’S 152°22’17’’E, 1.xi.2003 GoogleMaps .

Aural records (LWP). QUEENSLAND: Durikai State Forest (Thane), 28°10’41’’S 151°38’24’’E, 8.xi.2015 GoogleMaps . NEW SOUTH WALES: Torrington State Forest , 29°16’06’’S 151°39’55’’E, 6.i.2016 GoogleMaps .

Distribution, habitat and seasonality ( Fig. 1 View FIGURE 1 ). This species is restricted to southern coastal and northern montane areas in the northern half of New South Wales, extending north into adjacent areas of south-east Queensland. In New South Wales, it occurs from near Wyong west to Cassilis and north through the mountains east of Narrabri and the Armidale region to the Torrington area. In Queensland, it is known only from between Amiens and Thanes Creek, and near Killarney. Adults have been found between November and January.

Etymology. A Latin adjective (feminine), meaning ‘delicate’. This refers to the gracile appearance of this species relative to many of its congeners.

Description of adult male ( Plates 3A, 3B, 3G, 3I View PLATE 3 ; Figs 2D View FIGURE 2 , 3D View FIGURE 3 , 4D View FIGURE 4 , 12 View FIGURE 12 ).

Head slightly narrower than lateral margins of pronotum; mostly black with a yellow-orange triangular marking between lateral ocelli, based on posterior margin; two faint, brown markings between lateral ocelli and adjacent compound eyes, not reaching posterior margin; supra-antennal plates black, occasionally edged brown; ocelli pinkish-brown; postclypeus mainly black, inner dorsal side with a dull yellow-brown line extending from anterior margin almost to median ocellus; ventral side with pinkish-brown lateral margins; anteclypeus shiny black; rostrum reaching anterior edges of hind coxae, medium brown basally becoming dark brown apically; antennae dark brown to black.

Thorax mostly black. Pronotum with a narrow yellow-brown fascia along midline surrounded extensively by black; interior of pronotum dark brown, with irregular black areas, especially along paramedian and lateral fissures; pronotal collar black anteriorly, grading to brown towards posterior margin. Mesonotum brown, reddish-brown or black with black submedian and lateral sigilla; cruciform elevation pale brown to pale orange-brown apart from a broad black midline and black anterior arms; wing grooves mainly pale brown to brown. Metanotum orange and black. Thorax below mainly brown with leg cavities bordered dull orange-brown.

Legs mainly dark brown to orange-brown with black longitudinal markings. Fore coxae orange-brown on outer sides, dark brown on inner sides, with orange joints; mid hind coxae dark brown with orange joints; fore femora with inner side dark brown, outer side orange-brown, each with a dark brown longitudinal marking on ventral margin; femoral spines dark brown; mid and hind femora dark brown on anterior side, pale brown on posterior side; fore and mid tibiae dark brown to orange-brown; hind tibiae mainly brown to pale brown; tarsi brown; claws dark brown; meracantha black on basal half, pale brown and narrow apically, partially overlapping opercula.

Wings with fore wing costal margin orange-brown, tending pale orange-brown at node; CuP+1A pale brown basally, otherwise all venation dark brown to dark reddish-brown; basal membrane mostly orange, tending dull orange-grey distally. Hindwing venation brown to orange-brown; plagas and margin of jugum light brown to pale orange-brown.

Opercula ( Fig. 2D View FIGURE 2 ) black basally, plates brown to pale brown and broadly rounded; relatively small, each <1.9 mm wide.

Timbals ( Fig. 3D View FIGURE 3 ) with five long ribs all attached to basal spur and separated ventrally; long ribs 1–3 spanning the timbal membrane; long rib 4 may span the timbal membrane or appear discontinuous, with dorsal and ventral areas connected by only a very narrow medial area; long rib 5 shorter, occupying dorsal two thirds of timbal only; timbal plate with well developed, elongate dome bearing a distinct point of apodeme attachment near centre.

Abdomen mostly orange. Tergite 1 black; tergite 2 orange with black anterior margin and black medially extending to posterior margin, curved to follow outer margin of exposed timbals; tergites 3–7 predominantly orange, each with a black mark on dorsal midline, this narrowly and sometimes diffusely extending along posterior margins of lateral sides where it broadens into a diffuse black triangular marking, apex anterior facing; tergite 8 black. Sternite I mainly dull orange; sternite II mainly dark brown with dull orange areas ventrolaterally; sternites III–VI orange; sternite VII orange with a small, diffuse black spot at centre of posterior margin; sternite VIII dark brown becoming brown apically.

Genitalia ( Figs 4D View FIGURE 4 , 12 View FIGURE 12 ) with pygofer dark brown; upper lobe of moderate size, broad and broadly rounded at apex; basal pygofer lobe comparatively small, broadly rounded; median lobe of uncus well developed but not excessively long, slightly concave dorsally, in lateral view straight, narrow, parallel-sided; claspers robust, claw-like, in ventral view clearly separated, with apices gradually tapering laterally. Aedeagus with pseudoparameres not extending as far as theca; theca strongly recurved distally through 180 degrees towards apex, with transparent flanges along margin of recurvature, strongly serrated ventrolaterally and dorsolaterally towards apex; apex transparent, weakly upturned, sclerotised, spine-like, sometimes with sparse ornamentation.

Description of adult female ( Plates 3D, 3E, 3H View PLATE 3 ). Similar to male but differing as follows.

Abdomen appears black with orange lateral bands. Tergite 1 mainly black, sometimes with dark orange areas sublaterally; tergite 2 black suffused with orange laterally; tergite 3–7 predominantly orange, each with a broad black mark on dorsal midline, this mark extending along posterior margins of lateral sides where it broadens into a diffuse black triangular marking, apex anterior facing; tergite 8 mainly black with orange along posterior lateral margins. Sternite II mainly orange, dark brown medially; sternite III–VII orange. Abdominal segment 9 pale orange-brown, with a bold, black longitudinal marking on each side along the anterior lateral margin, extending posteriorly on dorsolateral sides. Ovipositor sheath dark reddish-brown to black, extending less than 0.5 mm beyond apex of abdominal segment 9.

Measurements (in mm; range with mean in parentheses for 10 typical males, 1 small male and 5 females, including smallest and largest specimens). Length of body including head: typical male 16.9–19.5 (18.27); small male 15.4; female 17.6–20.6 (19.80). Length of fore wing: typical male 20.2–23.7 (21.99); small male 18.5; female 23.1–25.7 (24.96). Width of fore wing: typical male 6.7–8.0 (7.46); small male 6.7; female 8.2–8.4 (8.26). Width of head (including eyes): typical male 4.8–5.6 (5.15); small male 4.1; female 5.2–6.0 (5.70). Width of pronotum (across lateral angles): typical male 4.8–5.9 (5.21); small male 4.3; female 5.0–6.5 (5.84). Width of abdomen: typical male 4.7–5.5 (5.08); small male 4.3; female 4.9–6.4 (5.78). Length of ovipositor: female 5.9–6.6 (6.22). The small male was treated separately as it was considered aberrant.

Morphological distinguishing features. Males of Y. delicata n. sp. can be distinguished from other species in the Y. tristrigata species group by the following combination of characters: (1) opercula relatively small, each <1.9 mm wide, (2) theca recurved distally through 180 degrees; and (3) apex of theca weakly upturned. Females can be distinguished from most other species in the Y. tristrigata species group by having the following combination of characters: (1) thorax mainly black, (2) fore wing length 23–26 mm, and (3) head width> 5.2 mm. They may be impossible to distinguish from specimens of Y. australicta n. sp. and Y. repetens , although none of these species have been found co-occurring.

Calling song ( Figs 13 View FIGURE 13 , 14 View FIGURE 14 ). Males of Yoyetta delicata n. sp. call almost entirely while stationary. They sometimes continue to call when moving a short distance between singing stations. The calling song is a loud buzz (long echeme) followed by a series of 2–19 (typically 10–14) syllables (all statistics, n =12 recordings). There is usually a pause of between 30 seconds and several minutes between phrases; however, it can be as little as 4 seconds. The duration of the long echeme is variable, between approximately 8 s and 90 s. The detailed structure of the long echeme (illustrated in Figs 13B View FIGURE 13 , 14B View FIGURE 14 ) shows a clearly defined train of prominent single pulses (with a pulse repetition rate of 59–125 Hz). These are reliably followed by a softer peak (or double peak), which may represent the sound produced by the relaxation of each timbal. The syllables that follow each long echeme vary from 0.03 to 0.09 s, are composed of 2–6 prominent pulses, and have a syllable repetition rate of 2–11 Hz. The durations of the syllables and the repetition rate often reduce successively towards the end of the phrase ( Figs 13C View FIGURE 13 , 14C View FIGURE 14 ). Female wing flick responses have been recorded 0.02– 0.03 s after a syllable (but not following all syllables and with no predictable pattern) in one cage recording (not illustrated).

As evidenced in some cage recordings, a soft “purring” echeme (or series of echemes) is sometimes produced at the end of a phrase after the syllables (not illustrated). These echemes have a pulse repetition rate of 20–55 Hz (lower than the long echeme) and appear to have a lower frequency than the rest of the calling song. These soft echemes are not evident in available field recordings and their behavioural role is not understood.

Based on a cage recording from the type locality, the calling song has a broad frequency plateau spanning approximately 10 to 13 kHz, with a dominant frequency of approximately 11.8 kHz ( Fig. 13 View FIGURE 13 ). In contrast, a recording from further north displays a higher broad frequency plateau from approximately 11 to 14 kHz, with a dominant frequency of approximately 13.1 kHz ( Fig. 14 View FIGURE 14 ). Differences in measured song frequencies may reflect difference in size of the insects, differences in recording situation (cage versus field) and/or differences in recording equipment. Despite the differences, the frequency spectra are broader than described here and mostly overlapping ( Figs 13 View FIGURE 13 , 14 View FIGURE 14 ).

Within the genus Yoyetta , the singing behaviour of Y. delicata n. sp. most closely resembles Y. serrata Emery, Emery & Popple , which is in the Y. abdominalis species group. The songs can easily be distinguished by the length of the gap between the long echeme and the first syllable, which is 20–50 ms in Y. delicata n. sp. and>300 ms in Y. serrata . Additionally, the phrases repeat much more regularly in Y. serrata , with little gap between them ( Emery et al., 2019) (cf. long and often irregular gaps between phrases in Y. delicata n. sp.).

AM

Australian Museum

T

Tavera, Department of Geology and Geophysics

ANIC

Australian National Insect Collection

JP

Phyletisches Museum Jena

MSM

Marine Science Museum, Tokai Univ.

R

Departamento de Geologia, Universidad de Chile

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Order

Hemiptera

Family

Cicadidae

SubFamily

Cicadettinae

Tribe

Cicadettini

Genus

Yoyetta

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