Euxaldar daweishanensis, Yang & Chang & Yang & Chen, 2021

Yang, Liang-Jing, Chang, Zhi-Min, Yang, Lin & Chen, Xiang-Sheng, 2021, A new species of the genus Euxaldar Fennah, 1978 (Hemiptera, Fulgoromorpha, Issidae) from China and revision on the molecular phylogeny of the family, ZooKeys 1021, pp. 19-35 : 19

publication ID

https://dx.doi.org/10.3897/zookeys.1021.35510

publication LSID

lsid:zoobank.org:pub:DE22C878-1AE5-4798-84B5-8FCB4A37A73B

persistent identifier

https://treatment.plazi.org/id/663A901A-6FF8-4BC9-A6B9-C9D1244AAB5B

taxon LSID

lsid:zoobank.org:act:663A901A-6FF8-4BC9-A6B9-C9D1244AAB5B

treatment provided by

ZooKeys by Pensoft

scientific name

Euxaldar daweishanensis
status

sp. nov.

Euxaldar daweishanensis View in CoL sp. nov. Figs 1-7 View Figures 1–7 , 8-17 View Figures 8–18 , 19-26 View Figures 19–26

Type material.

Holotype: ♂, China: Yunnan Province, Pingbian County, Mt: Daweishan National Nature Reserve (23°07'N, 103°20'E), 8 August, 2017, Qiang Luo, Nian Gong, Y. -J Sui, Yan Zhi. Paratypes GoogleMaps : 7♂♂ 36♀♀, same data as holotype GoogleMaps .

Measurements.

Total length (from apex of coryphe to tip of forewing): male 4.1-4.3 mm (N = 6), female 4.6-4.9 mm (N = 10); forewing length: male 3.8-4.0 mm (N = 7), female 4.2-4.4 mm (N = 10).

Diagnosis.

This species differs from other Euxaldar species by the following characters: (1) coryphe about 2.3 times wider than long (less, or more than 2.3 times as wide as long in other species of Euxaldar ); (2) first metatibiotarsal of hind leg with 8 intermediate spines (other species of Euxaldar with first metatarsomere of hind leg with 6 or 7 intermediate spines); (2) penis with 3 different ribbon-shaped processes at middle (Figs 16 View Figures 8–18 , 17 View Figures 8–18 , pp, paed), dorsal lobe of periandrium with 2 asymmetrical sword-shaped subapical processes in apical half (Figs 16 View Figures 8–18 , 17 View Figures 8–18 , sap) (other species without sword-shaped subapical processes in apical half of dorsal lobe of periandrium).

Coloration.

Male body brown yellowish, with irregular dark brown bands on forewings. Coryphe brown (Fig. 8 View Figures 8–18 ). Metope with all margins, pustules, and median carinae pale yellow, disc dark brown (Fig. 9 View Figures 8–18 ). Metopoclypeal suture light yellow. Anteclypeus straw yellow. Postclypeus pale yellow (Figs 9 View Figures 8–18 , 10 View Figures 8–18 ). Rostrum and antenna straw yellow (Fig. 10 View Figures 8–18 ). Eyes dark brown (Figs 8-10 View Figures 8–18 ). Pronotum straw yellow. Mesonotum dark brown (Fig. 8 View Figures 8–18 ). Forewings slightly hyaline, with 2 irregular brown bands (Figs 1 View Figures 1–7 , 2 View Figures 1–7 , 11 View Figures 8–18 ): a large one derived from costal margin to almost C2 of radial cell, small one derived from apical half of median cell, extended to areola postica (anterior cubital area). Legs (Figs 2 View Figures 1–7 , 4 View Figures 1–7 ) light brown. Abdomen brown, male genital segment light straw yellow. Females generally darker than males (Figs 3 View Figures 1–7 , 4 View Figures 1–7 ).

Head and thorax.

Coryphe transverse, about 2.3 times wider than long, anterior margin weakly prominent in the middle, posterior margin angularly concave (Fig. 8 View Figures 8–18 ). Metope flat, median carinae weak, running from upper margin and reaching middle, with a row of distinct pustules along lateral margins, disc with weak pustules (Fig. 9 View Figures 8–18 ). Metopoclypeal suture complete (Fig. 9 View Figures 8–18 ). Anteclypeus with distinct median carinae (Figs 9 View Figures 8–18 , 10 View Figures 8–18 ). Pronotum with disc depressed (Fig. 8 View Figures 8–18 ). Mesonotum about 2.1 times longer than pronotum. Forewings (Figs 1-4 View Figures 1–7 , 11 View Figures 8–18 ) with distinct claval suture and CuP venation, the other venation reticulate, poorly recognizable. Hind wings about 0.7 times as long as forewings, venation reticulate (Fig. 12 View Figures 8–18 ). Hind tibiae with 2 lateral teeth. Metatibiotarsal formula (9-8)-8-2.

Male genitalia.

Anal tube (Fig. 13 View Figures 8–18 ) enlarging from base to apical fourth in dorsal view, narrowing to apex, apical margin convex in the middle, laterally with 2 small triangular processes in apical fourth. Pygofer with hind margin distinctly convex (Figs 5 View Figures 1–7 , 14 View Figures 8–18 ). Gonostyli triangular, hind margin convex, caudo-dorsal angle rounded (Fig. 14 View Figures 8–18 ). Capitulum of gonostyli style with wide and short neck, with a wide lateral tooth and 2 apical teeth (Figs 14 View Figures 8–18 , 15 View Figures 8–18 ). Corpus of connective rod-like (Figs 5-7 View Figures 1–7 , 16 View Figures 8–18 , 17 View Figures 8–18 ), curved, cuticularized, reaching middle of periandrium; tectiductus of connective cup-shaped, third ventral part separated from corpus (Fig. 14 View Figures 8–18 ). Periandrium asymmetrical (Figs 6 View Figures 1–7 , 7 View Figures 1–7 , 16 View Figures 8–18 , 17 View Figures 8–18 ), suspensorium V-shaped in dorsal view, membranaceous in the middle; base with process claval (Figs 16 View Figures 8–18 , 17 View Figures 8–18 , bp), dorsal periandrium lobe with 2 ribbon-like processes in center near right edge (Figs 16 View Figures 8–18 , 17 View Figures 8–18 , pp), directed dorsad, respectively curved caudad and cephalad; dorsal lobe in left lateral view with 2 subapical processes near apex (Fig. 16 View Figures 8–18 , sap): one crescent-shaped, above base with another process shortly sword-shaped, directed caudad; in right lateral view (Fig. 17 View Figures 8–18 , sap) with two subapical processes derived from apical third, directed apically, one process base movable, sword-shaped, below base another process crutch-like and sclerotized. Ventral periandrium lobe (Fig. 18 View Figures 8–18 , vlp) with apical margin convex, shorter than dorso-lateral lobe of periandrium (Figs 16 View Figures 8–18 , 17 View Figures 8–18 , dllp, 18) in ventral view. Aedeagus (Figs 16 View Figures 8–18 , 17 View Figures 8–18 , aed) with dagger-shaped process, base slightly movable, directed dorsad, slightly inclined caudad (Figs 16 View Figures 8–18 , 17 View Figures 8–18 , paed).

Female genitalia.

Anal tube ovate in dorsal view, about 1.3 times longer than maximal width at second part (Fig. 19 View Figures 19–26 ). Anal style long, located at basal fifth of anal tube. In ventral view, Sternite VII with hind margin convex medially, without any process in ventral view, disc arched ventrad (Fig. 20 View Figures 19–26 ). Anterior connective lamina of gonapophysis VIII nearly rectangular, with 3 or 4 apical teeth on inner lateral margin and 3 lateral teeth bearing 3 keels on outer lateral margin (Figs 21 View Figures 19–26 , 22 View Figures 19–26 ); endogonocoxal lobe developed, membranous in distal part (Figs 21 View Figures 19–26 , 22 View Figures 19–26 ). Posterior connective lamina of gonapophyses IX triangular in dorsal view (Fig. 23 View Figures 19–26 ), narrowing; median field with leaf-like process bearing apical margin, deeply incised in the middle (Fig. 23 View Figures 19–26 , mdp); lateral field (Fig. 23 View Figures 19–26 , lf) without obvious process; distal parts of laminae (Fig. 23 View Figures 19–26 , slf) with tooth-like process on each lateral margin; posterior ventral lobes bent at slender angle (Figs 23 View Figures 19–26 , pvb, 24). Gonoplacs in lateral view irregularly elliptical (Fig. 25 View Figures 19–26 ), without carinae, with apical half fused, apical margin membranous (Fig. 26 View Figures 19–26 ).

Etymology.

This new species is named after the type locality, Mt. Daweishan National Nature Reserve , Yunnan Province, China.

Distribution.

China (Yunnan Province)

Remark.

This new species resembles Euxaldar jehucal but differs from the latter by the following combined features: Anal tube with apical margin convex in the middle, lateral margin with a small triangular process in each side (anal tube wide, apical margin deeply concave medially in E. jehucal ); periandrium with two asymmetrical subapical processes sword-shaped in apical half (periandrium with subapical processes not as sword-shaped in E. jehucal ); aedeagus with one medial dagger-like process on lateral margins (aedeagus without any processes on lateral margins in E. jehucal ).

Phylogenetical analysis.

Four gene fragments of Euxaldar daweishanensis sp. nov. were sequenced and registered in GenBank with the accession numbers as follows: MK 441660 View Materials ( COI), MK 426664 View Materials (16S), MK 441661 View Materials (Cytb), MK 441662 View Materials (28S d6-d7). Nucleotide compositions are listed in Table 3 View Table 3 . A+ T content of 16S is the highest (76.0%) and 28S (d6-d7) is the lowest (39.2%).

This study deals with more molecular markers from Oriental and Western Palaearctic, Nearctic and Neotropical regions than previous reviews by Wang et al. (2016) and Gnezdilov et al. (2020). BI (Fig. 27 View Figure 27 ) and ML (Fig. 28 View Figure 28 ) topologies were mostly congruent, and the monophyly of Issidae was reconfirmed. The Issidae had lower support in the ML tree ( BS: 47) than Gnezdilov et al. (2020) and Wang et al. et al. (2016) and higher support in the BL analysis ( PP: 88). Subfamilies Hysteropterinae Melichar, 1906 sensu ( Gnezdilov et al. 2020) and Issinae Spinola, 1839 sensu ( Gnezdilov et al. 2020) are both recovered (nodes 1 and 2: ML: 47, 67; BI: 88, 89, respectively).

Node 1 includes almost all tribal level genera group of the subfamily Hysteropterinae sensu Gnezdilov (2016a, b, 2020) and the tribe Thioniini Melichar, 1906 sensu ( Gnezdilov 2018): 1) Node 4 ( ML: 75, BI: 100) corresponds to the subtribe Thioniina sensu Gnezdilov (2018) with the inclusion of American taxa, characterized by hind wings reduced or rudimentary, A2 vein branched; 2) Nodes 5 and 6 corresponds to the monophyletic Kervillea , and Mycterodus genera group sensu Gnezdilov (2016 a, b); monophyly of the Hysteropterum genera group was not supported by this analysis (node 3).

Node 2 ( ML: 67, BI: 89) includes five monophyletic tribes (nodes 7-11): Issini , Kodaianellini and Hemisphaeriini sensu (Gnezdilov 2020), Parahiraciini , and Sarimini sensu ( Wang et al. 2016), while the monophyly of Sarimini and Parahiraciini was not supported by Gnezdilov (2020).

MK

National Museum of Kenya

COI

University of Coimbra Botany Department

T

Tavera, Department of Geology and Geophysics

ML

Musee de Lectoure

R

Departamento de Geologia, Universidad de Chile

MN

Museu Nacional, Universidade Federal do Rio de Janeiro

MW

Museum Wasmann

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Order

Hemiptera

Family

Issidae

Genus

Euxaldar