Neduba lucubrata Cole, Weissman, & Lightfoot, 2021

Cole, Jeffrey A., Weissman, David B., Lightfoot, David C., Ueshima, Norihiro, Warchałowska-Śliwa, Elżbieta, Maryańska-Nadachowska, Anna & Chatfield-Taylor, Will, 2021, A revision of the shield-back katydid genus Neduba (Orthoptera: Tettigoniidae: Tettigoniinae: Nedubini), Zootaxa 4910 (1), pp. 1-92 : 55-57

publication ID

https://doi.org/ 10.11646/zootaxa.4910.1.1

publication LSID

lsid:zoobank.org:pub:69A0204C-15B4-4566-AA27-E3817087130A

DOI

https://doi.org/10.5281/zenodo.4465046

persistent identifier

https://treatment.plazi.org/id/039C87AE-7D40-FFFF-FF47-07CF7539FC91

treatment provided by

Plazi

scientific name

Neduba lucubrata Cole, Weissman, & Lightfoot
status

sp. nov.

Neduba lucubrata Cole, Weissman, & Lightfoot View in CoL , sp. n.

Fig. 19 View FIGURE 19 (distribution), Fig. 23 View FIGURE 23 (male and female habitus, calling song, drumming, male and female terminalia, karyotype), Plate 2E View PLATE 2 (live habitus), Plate 5C View PLATE 5 (male calling song), Plate 7 View PLATE 7 G–H (male ventral sclerites), Plate 10D View PLATE 10 (male titillators), Plate 12A View PLATE 12 (female subgenital plate).

Common name. Midnight Shieldback.

History of recognition. None.

Type material. HOLOTYPE MALE, USA, CA, Monterey Co., Miller’s Lodge , 0.6 miles west jct. Arroyo Seco Road and G16, 36.25466N, 121.43208W, 192 m, 22-VII-2015, JA Cole, DB Weissman, JAC000002197 [specimen barcode], DNA161 [tissue], SING0503 [DNA extraction], JCT15-08 View Materials [karyotope], genitalia in vial under specimen, deposited in CAS, Entomology type #19712. GoogleMaps

PARATYPES (n = 32): All USA, CA , Monterey Co., 4♁, 1♀, same data as holotype, LACM GoogleMaps ; 2♁, 1♀, Arroyo Seco Rd. , 0.6 mi. W of intersection with G16, 36.235139N, 121.473392W, 274 m, 29-VII-1983, DB Weissman, CAS GoogleMaps ; 3♁, Bottcher’s Gap, Los Padres National Forest, 19 miles north of Big Sur off SR1 on Palo Colorado Road , 36.355N, 121.8138W, 652 m, 20-21-VIII-2012, JA Cole, LACM GoogleMaps ; 1♁, same data except 7-8-IX-2002, JA Cole, LACM GoogleMaps ; 7♁, Nacimiento-Ferguson Rd., at bridge of Nacimiento River , 8.4 miles east of SR1, 36.0135N, 121.4216W, 587 m, 19-20-VIII-2012, JA Cole, LACM GoogleMaps ; San Benito Co., 9♁, Short Fence Trailhead, Coalinga Road , Laguna Mountain Recreation Area , BLM, 36.36403N, 120.8784W, 670 m, 10-11-VIII-2017, JA Cole, LACM GoogleMaps ; 2♁, same data except 10-11-VIII-2017, JA Cole, JAC GoogleMaps ; 2♁, Upper Sweetwater Campground, Coalinga Road, Laguna Mountain Recreation Area , BLM, 36.36067N, 120.85256W, 848 m, 10-11-VIII-2017, JA Cole, LACM GoogleMaps .

Measurements. (mm, ♁n = 24, ♀ n = 2) Hind femur ♁16.35–20.74, ♀ 21.61–22.90, pronotum total length ♁7.04–9.03, ♀ 8.95–9.17, prozona length ♁2.65–4.78, ♀ 4.02–4.18, metazona dorsal length ♁3.85–5.10, ♀ 4.77– 5.15, pronotum constriction width ♁1.85–2.66, ♀ 2.70–3.35, metazona dorsal width ♁5.36–6.25, ♀ 5.76–6.35, head width ♁3.90–4.70, ♀ 5.11–5.46, ovipositor length ♀ 16.50–16.60.

Distribution. Santa Lucia and Diablo Ranges in the South Coast Range, California.

Habitat. Mixed woodland and chaparral. Taken from twigs in tangles, poison oak, and California sage ( Artemisia californica Less. ). Males call approximately 1 m above ground level in thick tangles. At dusk two males and one female emerged for nocturnal activity from a pack rat nest, suggesting that this structure served as a daytime shelter for an aggregation of individuals. These individuals retreated into the nest when disturbed.

Seasonal occurrence. Adults from late July (22-VII-2015, JA Cole and DB Weissman, LACM) through early September (8-IX-2002, JA Cole, LACM).

Stridulatory file. (n = 7) length 3.2–3.8 mm, 121–186 teeth, tooth density 45.9 ± 4.2 (38.4–50.0) teeth/mm.

Song. (n = 31) Brief bouts separated by long intervals between bouts. PTR is 4.0 ± 0.5 s- 1. Males may add one PT to each successive bout, for example three successive bouts may consist of 3 PT, 4 PT, then 5 PT, and then the cycle recommences at 3 PT. PTF is 14.9 ± 0.8 kHz. Males may accompany stridulation with audible drumming, which is generated by the abdomen striking the substrate ( Weissman 2001; JAC pers. obs.). Drumming coincides with partial PT at the beginning of a bout ( Fig. 23 View FIGURE 23 ). Drumming does not occur frequently and may not occur in all populations. Drumming was observed at the Monterey County localities of Arroyo Seco (one of two males, DBW, JAC, pers. obs.) and Bottcher’s Gap ( JAC, pers. obs.), but not at any San Benito County localities .

Karyotype. (n = 8) Unique. 2n♁ = 24 (2m + 20t + XtYt). T83-37, S83-107, paratopotype.

Recognition. With a single apical protibial spine, dark apical tegminal spots and prosternal spines, this species may be confused only with N. propsti , a larger species that does not occur on the California mainland. The female subgenital plate length and width are subequal, in contrast with the elongated subgenital plate of N. propsti . The song, which consists of short stridulation bouts accompanied by drumming, is unique.

Etymology. l. lucubrata burning the midnight oil, descriptive of male acoustic activity continuing throughout the night.

Notes. This species shares morphological and genitalic characteristics with N. propsti as well as with the species of the Sierranus and Castanea Groups. Santa Lucia Range and Diablo Range populations are genetically distinct ( Figs. 3–5 View FIGURE 3 View FIGURE 4 View FIGURE 5 ) but are separable neither morphologically nor bioacoustically. The chirping song structure combined with abdominal drumming makes N. lucubrata the most acoustically distinct species of Neduba . Selection for mate recognition may have driven the evolution of distinctive song phrasing in N. lucubrata , as within its distribution are found two sympatric nedubines: N. carinata and a small Aglaothorax species. Females may require silent periods of an appropriate intermediate length between bouts to recognize a conspecific male signal (Cole 2016): intermediate length gaps between PT bouts will contrast with the continuous PT production of sympatric N. carinata as well and the long periods of silence between pulse production in Aglaothorax .

Material examined. Type series only. See Type material above.

Sierranus Group

The Sierranus Group is composed of 3 species ( sierranus , arborea , and radocantans ). Like the Sequoia Group, all Sierranus Group species have a single spine on the posterior margin of the forefemur, a pair of prosternal spines, and the entire male tegmen ivory or white. The male subgenital plate has lateral carinae that converge to the apex, which is devoid of styli, petal-like and often reflexed. The stridulatory file tooth density is the highest of all Neduba species groups (59–77 teeth/mm), and this character alone separates it from all Sequoia Group species except N. inversa . The Sierranus Group is distributed in the central and northern Sierra Nevada while the Sequoia Group occupies the southern portions of that mountain range ( Figs. 8 View FIGURE 8 , 19 View FIGURE 19 ). Within this Group are morphologically cryptic species defined by song and/or karyotype. Body part measurements and stridulatory files offer the only means to identify males that lack song data. Females may also be identified by body part measurements and sometimes the shape of the subgenital plate. Species are parapatric in the Sierra Nevada ( Fig. 19 View FIGURE 19 ) and thus geography will serve to narrow species possibilities. Molecular data show hybridization ( Fig. 4 View FIGURE 4 ) between species with adjacent ranges.

CA

Chicago Academy of Sciences

CAS

California Academy of Sciences

LACM

Natural History Museum of Los Angeles County

JAC

University of Jodhpur

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Order

Orthoptera

Family

Tettigoniidae

Genus

Neduba

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