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Genus Vrsanskysajda nom. nov. Sajda Vršanský, 2021: 27 (Blattaria: Corydiidae: Holocompsinae). Preoccupied by Sajda Dworakowska, 1981: 244 (Homoptera: Cicadellidae: Typhlocybinae). Type species: Vrsanskysajda equatorialis (Vršanský in Vršanský et al. 2021) comb. nov. Etymology. The replacement name for the genus is derived from the name of Peter Vršanský, the author of the genus Sajda. Gender: feminine. Distribution. Brezina, Algeria., Published as part of Jiang, Lina, Xing, Jichun & Li, Yujian, 2023, New replacement name for the genus Sajda Vršanský, 2021 (Blattaria: Corydiidae: Holocompsinae), pp. 343-344 in Zootaxa 5270 (2) on page 343, DOI: 10.11646/zootaxa.5270.2.10, http://zenodo.org/record/7849704, {"references":["Vrsansky, P., Vrsanska, L., Vasilenko, D. V., Puskelova, L. & Biron, A. (2021) An isolated Cretaceous analogue of Madagascar on the Adria - Turkey microcontinent indicated by fossils in Brezina, Algeria. Palaeontographica, Abteilung A. Palaozoologie-Stratigraphie, 321 (1 / 6), 19 - 35. https: // doi. org / 10.1127 / pala / 2021 / 0107","Dworakowska, I. (1981) Proskura gen. n. and some Erythroneurini from Souther India (Homoptera, Auchenorrhyncha, Cicadellidae, Typhlocybinae). Reichenbachia, 19 (37), 225 - 246."]}

Zanolkyra guaira (Zanol, 2011) Kyra guaira Zanol, 2011:3 Zanolkyra guaira (Zanol, 2011), Yang 2017: 133 Parakyra guaira (Zanol, 2011), Dmitriev 2020: 35, Published as part of Cao, Wenjun & Xing, Jichun, 2022, Synonymy of Parakyra Dmitriev, 2020 with Zanolkyra Yang, 2017 (Hemiptera Cicadellidae: Deltocephalinae: Bahitini), pp. 95-96 in Zootaxa 5195 (1) on page 95, DOI: 10.11646/zootaxa.5195.1.7, http://zenodo.org/record/7180708, {"references":["Zanol, K. M. R. (2011) Kyra gen. nov. (Cicadellidae, Deltocephalinae) and descriptions of two new species. Acta Biologica Paranaense Curitiba, 40 (1 - 2), 1 - 8. https: // doi. org / 10.5380 / abpr. v 40 i (1 - 4). 25199","Yang, W. C. (2017) New replacement name for Kyra Zanol, 2011 (Hemiptera: Cicadellidae: Deltocephalinae). Zootaxa, 4299 (1), 133 - 134. https: // doi. org / 10.11646 / zootaxa. 4299.1.8","Dmitriev, D. A. (2020) Nomenclatural changes in the suborders Auchenorrhyncha (Hemiptera) and Paleorrhyncha (Palaeohemiptera). Zootaxa, 4881 (1), 25 - 53. https: // doi. org / 10.11646 / zootaxa. 4881.1.2"]}

Zanolkyra Yang, 2017 Kyra Zanol, 2011: 1. Zanolkyra Yang, 2017: 133, nomen novum for Kyra Zanol, 2011, preoccupied by Eurhodope (Kyra) Gozmány, 1958. Parakyra Dmitriev, 2020: 34, nomen novum for Kyra Zanol, 2011, preoccupied by Eurhodope (Kyra) Gozmány, 1958. syn. nov. Type species: Kyra paranaigua Zanol, 2011 Distribution. Brazil., Published as part of Cao, Wenjun & Xing, Jichun, 2022, Synonymy of Parakyra Dmitriev, 2020 with Zanolkyra Yang, 2017 (Hemiptera Cicadellidae: Deltocephalinae: Bahitini), pp. 95-96 in Zootaxa 5195 (1) on page 95, DOI: 10.11646/zootaxa.5195.1.7, http://zenodo.org/record/7180708, {"references":["Yang, W. C. (2017) New replacement name for Kyra Zanol, 2011 (Hemiptera: Cicadellidae: Deltocephalinae). Zootaxa, 4299 (1), 133 - 134. https: // doi. org / 10.11646 / zootaxa. 4299.1.8","Zanol, K. M. R. (2011) Kyra gen. nov. (Cicadellidae, Deltocephalinae) and descriptions of two new species. Acta Biologica Paranaense Curitiba, 40 (1 - 2), 1 - 8. https: // doi. org / 10.5380 / abpr. v 40 i (1 - 4). 25199","Gozmany, L. (1958) Notes on Hungarian Phycitidae (Lepidoptera). Annales Historico-Naturales Musei Hungarici, New Series, 9, 223 - 225.","Dmitriev, D. A. (2020) Nomenclatural changes in the suborders Auchenorrhyncha (Hemiptera) and Paleorrhyncha (Palaeohemiptera). Zootaxa, 4881 (1), 25 - 53. https: // doi. org / 10.11646 / zootaxa. 4881.1.2"]}

Zanolkyra paranaigua (Zanol, 2011) Kyra paranaigua Zanol, 2011:2 Zanolkyra paranaigua (Zanol, 2011), Yang 2017: 133 Parakyra paranaigua (Zanol, 2011), Dmitriev 2020: 35 Zanolkyra umbrina (Linnavuori, 1955) Bahita umbrina Linnavuori, 1955: 115 Parabahita umbrina (Linnavuori, 1955), Linnavuori 1959: 178; Linnavuori & DeLong 1978: 128 Kyra umbrina (Linnavuori, 1955), Zanol 2011: 3 Zanolkyra umbrina (Linnavuori, 1955), Yang 2017: 133 Parakyra umbrina (Linnavuori, 1955), Dmitriev 2020: 35, Published as part of Cao, Wenjun & Xing, Jichun, 2022, Synonymy of Parakyra Dmitriev, 2020 with Zanolkyra Yang, 2017 (Hemiptera Cicadellidae: Deltocephalinae: Bahitini), pp. 95-96 in Zootaxa 5195 (1) on page 95, DOI: 10.11646/zootaxa.5195.1.7, http://zenodo.org/record/7180708, {"references":["Zanol, K. M. R. (2011) Kyra gen. nov. (Cicadellidae, Deltocephalinae) and descriptions of two new species. Acta Biologica Paranaense Curitiba, 40 (1 - 2), 1 - 8. https: // doi. org / 10.5380 / abpr. v 40 i (1 - 4). 25199","Yang, W. C. (2017) New replacement name for Kyra Zanol, 2011 (Hemiptera: Cicadellidae: Deltocephalinae). Zootaxa, 4299 (1), 133 - 134. https: // doi. org / 10.11646 / zootaxa. 4299.1.8","Dmitriev, D. A. (2020) Nomenclatural changes in the suborders Auchenorrhyncha (Hemiptera) and Paleorrhyncha (Palaeohemiptera). Zootaxa, 4881 (1), 25 - 53. https: // doi. org / 10.11646 / zootaxa. 4881.1.2","Linnavuori, R. (1955) Contributions to the Neotropical leafhopper fauna of the family Cicadellidae IV. (Continued.). Suomen Hyonteistieteellinen Aikakauskirja. Annales Entomologici Fennici, 21,113 - 129.","Linnavuori, R. (1959) Revision of the Neotropical Deltocephalinae and some related subfamilies. Annales Botanici Societatis Zoologicae Botanicae Fennicae Vanamo, 20 (1), 1 - 370.","Linnavuori, R. & DeLong, D. M. (1978) Neotropical leafhoppers of the Bahita group (Homoptera: Cicadellidae: Deltocephalinae); a contribution to the taxonomy. Brenesia, 14 - 15, 109 - 169."]}

Tambocerus robustispinus Qu & Dai, 2014 Tambocerus robustispinus Qu & Dai, 2014: 53. Distribution. China (Guangxi, Yunnan). Material examined. Holotype, ♂, CHINA: Guangxi Autonomous Region, Wuming County, Damingshan National Natural Reserve, 15 May 2012, coll. Hu Li (GUGC). Paratypes, 6 ♂♂, same data as holotype (GUGC); 1 ♂, Yunnan Prov., Yuanyang County, Shangjiupai, 2 August 2013, coll. Yangyang Liu., Published as part of Yao, Binbin, Dietrich, Christopher H. & Xing, Jichun, 2022, Description of a new species of the leafhopper genus Tambocerus (Hemiptera: Cicadellidae: Deltocephalinae) from Guizhou, China, pp. 87-92 in Zootaxa 5169 (1) on page 91, DOI: 10.11646/zootaxa.5169.1.8, http://zenodo.org/record/6911353, {"references":["Qu, L. & Dai, R. H. (2014) Three new species of the leafhopper genus Tambocerus Zhang & Webb (Hemiptera, Cicadellidae) from southern China. ZooKeys, 434, 47 - 55."]}

Tambocerus furcellus Shang & Zhang, 2008 Tambocerus furcellus Shang & Zhang, 2008: 247. Distribution. China (Hunan)., Published as part of Yao, Binbin, Dietrich, Christopher H. & Xing, Jichun, 2022, Description of a new species of the leafhopper genus Tambocerus (Hemiptera: Cicadellidae: Deltocephalinae) from Guizhou, China, pp. 87-92 in Zootaxa 5169 (1) on page 91, DOI: 10.11646/zootaxa.5169.1.8, http://zenodo.org/record/6911353

Tambocerus dentatus Qu & Dai, 2014 Tambocerus dentatus Qu & Dai, 2014: 51. Distribution. China (Guizhou). Material examined. Holotype, ♂, CHINA: Guizhou Prov., Libo County, 20 July 2011, coll. Weibin Zheng (GUGC)., Published as part of Yao, Binbin, Dietrich, Christopher H. & Xing, Jichun, 2022, Description of a new species of the leafhopper genus Tambocerus (Hemiptera: Cicadellidae: Deltocephalinae) from Guizhou, China, pp. 87-92 in Zootaxa 5169 (1) on page 89, DOI: 10.11646/zootaxa.5169.1.8, http://zenodo.org/record/6911353, {"references":["Qu, L. & Dai, R. H. (2014) Three new species of the leafhopper genus Tambocerus Zhang & Webb (Hemiptera, Cicadellidae) from southern China. ZooKeys, 434, 47 - 55."]}

Tambocerus longicaudatus Qu & Dai, 2014 Tambocerus longicaudatus Qu & Dai, 2014: 52. Distribution. China (Guizhou). Material examined. Holotype, ♂, CHINA: Guizhou Prov., Suiyang County, Kuankuoshui National Natural Reserve, 5 June 2010, coll. Jichun Xing (GUGC); Paratype, 1 ♂, CHINA: Guizhou Province, Suiyang County, Kuankuoshui National Natural Reserve, 8 June 2010, coll. Renhuai Dai and Hu Li., Published as part of Yao, Binbin, Dietrich, Christopher H. & Xing, Jichun, 2022, Description of a new species of the leafhopper genus Tambocerus (Hemiptera: Cicadellidae: Deltocephalinae) from Guizhou, China, pp. 87-92 in Zootaxa 5169 (1) on page 91, DOI: 10.11646/zootaxa.5169.1.8, http://zenodo.org/record/6911353, {"references":["Qu, L. & Dai, R. H. (2014) Three new species of the leafhopper genus Tambocerus Zhang & Webb (Hemiptera, Cicadellidae) from southern China. ZooKeys, 434, 47 - 55."]}

Tambocerus fanjingensis sp. nov. (Figs 1–12) Description. Color pattern typical for genus.Vertex with median length 0.35x basal width between eyes. Head in dorsal view slightly narrower than pronotum. Fore femur with one dorsoapical seta, row AM with 2 stout setae, and row IC with 3 stout setae and several short setae. Hind femur setal formula 2+2+1. Hind tibia row PD with 21 macrosetae; row AD with approximately 13 long stout setae and 0–4 short and stout setae between each long seta. Male genitalia. Pygofer elongate, triangularly produced into straight spinelike process posteriorly, with scattered fine setae (Figs 5, 6). Valve triangular (Fig. 7). Subgenital plate abruptly narrowing at midlength, apical half slender with three stout macrosetae and several short setae (Fig. 8). Aedeagal shaft in ventral view broad, 1/3 as wide as long in ventral view, lateral margins with serrations (Fig. 9); aedeagus in lateral view strongly curved dorsally, Cshaped, apex expanded with a small triangular lamellar process in lateral view (Fig. 10); gonopore apical (Figs 9, 10). Connective stem twice as long as arms (Fig. 11). Style broad at base, abruptly narrowing subapically, preapical lobe with setae (Fig. 12). Measurement. Length (including tegmen): ♂, 6.6–6.8 mm. Host plant. Grasses. Type material. Holotype: ♂, CHINA: Guizhou Prov., Jiangkou County, Mt. Fanjing, 30 May 2021, coll. Binbin Yao (GUGC). Paratypes: 2♂♂, same data as holotype (GUGC). Remarks. The new species is similar to T. robustispinus Qu & Dai, 2014, but can be distinguished from the later by the relatively broad, parallel-sided aedeagal shaft in posterior view with the lateral margins serrate throughout their length and the apex lacking distinct processes. Etymology. This new species is named after its type locality “Fanjing”.

Tambocerus elongatus Shen, 2008 Tambocerus elongatus Shen, 2008: 243. Distribution. China (Hunan, Shaanxi, Hainan, Fujian, Hubei, Anhui, Guangxi and Henan)., Published as part of Yao, Binbin, Dietrich, Christopher H. & Xing, Jichun, 2022, Description of a new species of the leafhopper genus Tambocerus (Hemiptera: Cicadellidae: Deltocephalinae) from Guizhou, China, pp. 87-92 in Zootaxa 5169 (1) on page 89, DOI: 10.11646/zootaxa.5169.1.8, http://zenodo.org/record/6911353, {"references":["Shen, L., Shang, S. Q. & Zhang, Y. L. (2008) Study of the leafhopper genus Tambocerus (Hemiptera: Cicadellidae) with four new species from China. Proceedings of the Entomological Society of Washington, 110, 242 - 249. https: // doi. org / 10.4289 / 0013 - 8797 - 110.1.242"]}

Tambocerus quadricornis Shang & Zhang, 2008 Tambocerus quadricornis Shang & Zhang, 2008: 248. Distribution. China (Guangxi)., Published as part of Yao, Binbin, Dietrich, Christopher H. & Xing, Jichun, 2022, Description of a new species of the leafhopper genus Tambocerus (Hemiptera: Cicadellidae: Deltocephalinae) from Guizhou, China, pp. 87-92 in Zootaxa 5169 (1) on page 91, DOI: 10.11646/zootaxa.5169.1.8, http://zenodo.org/record/6911353

Tambocerus triangulatus Shen, 2008 Tambocerus triangulatus Shen, 2008: 246. Distribution. China (Shaanxi, Hainan)., Published as part of Yao, Binbin, Dietrich, Christopher H. & Xing, Jichun, 2022, Description of a new species of the leafhopper genus Tambocerus (Hemiptera: Cicadellidae: Deltocephalinae) from Guizhou, China, pp. 87-92 in Zootaxa 5169 (1) on page 91, DOI: 10.11646/zootaxa.5169.1.8, http://zenodo.org/record/6911353, {"references":["Shen, L., Shang, S. Q. & Zhang, Y. L. (2008) Study of the leafhopper genus Tambocerus (Hemiptera: Cicadellidae) with four new species from China. Proceedings of the Entomological Society of Washington, 110, 242 - 249. https: // doi. org / 10.4289 / 0013 - 8797 - 110.1.242"]}

Tambocerus Zhang & Webb, 1996 Tambocerus Zhang & Webb, 1996: 8; Shen, Shang & Zhang, 2008: 243; Viraktamath, 2012: 44; Qu & Dai, 2014: 48; Naveed & Zhang, 2018: 237. Type species: Selenocephalus disparatus Melichar, 1903. Diagnosis. Tambocerus can be distinguished by the following combination of characters: body robust, yellow with numerous small brown irregular spots; vertex slightly produced medially, with transverse ridges on anterior margin; male pygofer lobe serrate or with tooth- or spine-like process; connective Y-shaped with stem longer than arms; and aedeagal shaft with lateral margins serrated. Distribution. China, India, Sri Lanka, Pakistan. Notes. The tribal placement of Tambocerus has been controversial. Zhang & Webb (1996) placed the genus in the tribe Selenocephalini based on the fore margin of the head with transverse striations. It was transferred to the rather poorly characterized deltocephaline tribe Athysanini (Viraktamath, 2012). However, the recent phylogenomic analysis of Cao et al. (2022) consistently placed Tambocerus in together with the Afrotropical genus Odzalana Linnavuori (currently placed in Drabescini) and the Oriental genera Sychentia Wei & Webb (placed in Stegelytrini) and Orientus DeLong (placed in Athysanini) in a clade sister to a larger lineage of mostly Afrotropical genera (tribes Penthimiini in part, Bonaspeiini and Selenocephalini). Thus, the tribal placement of Tambocerus should be considered uncertain at present., Published as part of Yao, Binbin, Dietrich, Christopher H. & Xing, Jichun, 2022, Description of a new species of the leafhopper genus Tambocerus (Hemiptera: Cicadellidae: Deltocephalinae) from Guizhou, China, pp. 87-92 in Zootaxa 5169 (1) on page 88, DOI: 10.11646/zootaxa.5169.1.8, http://zenodo.org/record/6911353, {"references":["Zhang, Y. L. & Webb, M. D. (1996) A revised classification of the Asian and Pacific Selenocephalinae leafhoppers (Homoptera: Cicadellidae). Bulletin of the Natural History Museum (Entomology), 65 (1), 1 - 103.","Shen, L., Shang, S. Q. & Zhang, Y. L. (2008) Study of the leafhopper genus Tambocerus (Hemiptera: Cicadellidae) with four new species from China. Proceedings of the Entomological Society of Washington, 110, 242 - 249. https: // doi. org / 10.4289 / 0013 - 8797 - 110.1.242","Viraktamath, C. A. (2012) Seven new species of the leafhopper genus Tambocerus (Hemiptera: Cicadellidae) from the Indian subcontinent. Zootaxa, 3385 (1), 43 - 61. https: // doi. org / 10.11646 / zootaxa. 3385.1.4","Qu, L. & Dai, R. H. (2014) Three new species of the leafhopper genus Tambocerus Zhang & Webb (Hemiptera, Cicadellidae) from southern China. ZooKeys, 434, 47 - 55.","Naveed, H. & Zhang, Y. L. (2018) A key to species of the leafhopper genus Tambocerus (Hemiptera, Cicadellidae, Deltocephalinae) with description of a new species from Pakistan. Zootaxa, 4462 (2), 237 - 244. https: // doi. org / 10.11646 / zootaxa. 4462.2.5","Melichar, L. (1903) Homopteren-Fauna von Ceylon. F. L. Dames, Berlin, 248 pp.","Cao, Y., Dietrich, C. H., Zahniser, J. N. & Dmitriev, D. A. (2022) Dense sampling of taxa and characters improves phylogenetic resolution among deltocephaline leafhoppers (Hemiptera: Cicadellidae: Deltocephalinae). Systematic Entomology, 47, 430 - 444. https: // doi. org / 10.1111 / syen. 12540"]}

Genus Bambusaecoccus Meng & Xing gen. n. Type species: Bambusaecoccus maolanensis Meng & Xing sp. n., here designated. Generic diagnosis of adult female. Body broadly oval. Anal cleft deep, about 1/4‒1/5th of total body length. Stigmatic clefts present, deep, narrow marginally, but broadening away from margin, each cleft associated with about 20 dorsal stigmatic spines, with sclerotisation around inner margin, and in a small dorsal area. Dorsal derm membranous with numerous areolations. Dorsal setae short and sparse. Preopercular pores present in 2 groups, each group present antero-lateral to anal plates. Anal plates together quadrate, slightly pyriform, each plate with anterolateral margin slightly longer than posterolateral margin. Marginal setae apparently ventral, each short and spinose. Ventral tubular ducts present in a small group lateral to genital opening. Pregenital disc pores mostly each with 5‒8 loculi, present in a small group beneath posterior end of anal plates. Antennae small, each 7 segmented. Legs greatly reduced, each with only 3 segments visible on available material. Etymology. The name Bambusaecoccus is composed of the main part of the plant subfamily Bambusoideae on which the type species was collected, plus ‘ coccus ’, from the Greek word “ kokkos ” meaning “seed” or “scale insect”. Distribution. China. Remarks. The soft scale insect tribe Paralecaniini contains genera characterized by possession of a pair of eyespots on the dorsal surface of the head, situated some distance from the margin; and stigmatic clefts noticeably sunken and well sclerotized (Williams 1969). The tribe was revised by Hodgson (1994: 48), who listed four additional characteristics: “(i) lack of dorsal tubular ducts; (ii) restriction of ventral tubular ducts, if present, to a group on either side of genital opening; (iii) lack of pocket-like sclerotizations (except in Perilecanium); and (iv) restriction of pregenital disc-pores to segments immediately anterior to genital opening (when present)”. Bambusaecoccus possesses all of the above characteristics of the Paralecaniini: the adult females lack dorsal tubular ducts, and have a pair of eyespots on the dorsal surface of the head situated some distance from the margin; ventral tubular ducts are restricted to a small group on either side of the genital opening; and pregenital disc-pores are restricted to segments immediately anterior to the genital opening. Bambusaecoccus is similar to Takahashilecanium Kondo (in Kondo et al. 2005) in sharing the following character states: (i) stigmatic clefts present; (ii) pregenital disc-pores mostly each with 5 loculi; (iii) anal plates together pyriform; (iv) spiracular disc-pores present in broad bands between margin and spiracles; (v) preopercular pores present in two groups located laterad to anal plates; and (vi) pregenital disc pores forming a small group posterior to vulvar opening on each side of the anal cleft. Bambusaecoccus can be distinguished from the latter genus by (character states of Takahashilecanium in brackets): (i) stigmatic clefts each associated with about 20 dorsal stigmatic spines (each cleft containing only 3 stigmatic spines); (ii) ventral tubular ducts present in a small group on each side of genital opening (ventral tubular ducts absent); and (iii) legs and antennae reduced (legs and antennae well developed, although small relative to body size)., Published as part of Meng, Shitao & Xing, Jichun, 2022, Bambusaecoccus maolanensis, a new soft scale genus and species from China (Hemiptera: Coccomorpha: Coccidae), pp. 419-430 in Zootaxa 5168 (4) on pages 420-421, DOI: 10.11646/zootaxa.5168.4.2, http://zenodo.org/record/6899711, {"references":["Williams, D. J. (1969) The family-group names of the scale insects (Hemiptera: Coccoidea). Bulletin of the British Museum (Natural History) Entomology, 23, 315 - 341. https: // doi. org / 10.5962 / bhl. part. 15136","Hodgson, C. J. (1994) The Scale Insect Family Coccidae: An Identification Manual to Genera. CAB International, Wallingford, 639 pp.","Kondo, T., Williams, M. L. & Gullan, P. J. (2005) Taxonomic review of the genus Xenolecanium Takahashi and description of the new genus Takahashilecanium Kondo (Hemiptera: Coccidae; Coccinae, Paralecaniini). Entomological Science, 8, 109 - 120. https: // doi. org / 10.1111 / j. 1479 - 8298.2005.00105. x"]}

Key to genera of Paralecaniini (Coccinae) found in the Palaearctic and Oriental Regions based on adult females, adapted from Hodgson (1994) and Kondo (2005). 1(0) Dorsal setae each shorter than width of basal socket; pregenital disc-pores absent.................................. 2 - Dorsal setae each longer than width of basal socket; pregenital disc-pores present or absent.......................... 3 2(1) Legs reduced; anal plates together distinctly quadrate with outer margins angular, each plate about as long as their combined widths; claw digitules both fine............................................................ Saccharolecanium - Legs normal; anal plates together approximately diamond-shaped, each anal plate with outer margin rounded, and longer than their combined widths; claw digitules both broad.................................................... Maacoccus 3(1) Preopercular pores absent............................................................................... 4 - Preopercular pores present.............................................................................. 7 4(3) Marginal setae broadly fan shaped.............................................................. Paralecanium - Marginal setae narrow, not broadly fan shaped.............................................................. 5 5(4) Legs and antennae reduced to stumps; dorsal setae very small, each situated on a raised dermal cone......... Platylecanium - Legs and antennae well developed; dorsal setae normal size, each not situated on a raised dermal cone.................. 6 6(5) Each stigmatic cleft with a group of fleshy protuberances on either side; stigmatic spines spinose............. Anthococcus - Stigmatic clefts normal, each without a group of fleshy protuberances on either side; shape of stigmatic spines distinctive, either broadly wedge-shaped or bluntly tubular....................................................... Pounamococcus 7(3) Preopercular pores forming 1 or 2 longitudinal bands......................................................... 8 - Preopercular pores forming 2 groups, each situated antero-lateral to anal plates.................................... 9 8(7) Each stigmatic cleft without stigmatic spines, or with 1 stigmatic spine on anterior margin................. Perilecanium - Each stigmatic cleft with 2 stigmatic spines, each situated at a basal corner............................. Marsipococcus 9(7) Anal cleft with sides closely adpressed or fused together........................................... Megalocryptes - Anal cleft with sides not closely adpressed or fused together.................................................. 10 10(9) Pregenital setae represented by a band of multiple setae...................................................... 11 - Pregenital setae represented by 3 pairs of long setae......................................................... 12 11(10) Legs and antennae reduced; ventral tubular ducts present in a small group on each side of genital opening; dorsal sclerotic plates absent........................................................................... Bambusaecoccus gen. n. - Legs and antennae well developed, although small relative to body size; ventral tubular ducts absent; dorsum with triangular to irregular-shaped sclerotic plates............................................................ Takahashilecanium 12(10) Ventral tubular ducts present, each with inner ductule swollen and lacking a terminal gland; each stigmatic cleft with stigmatic spines present as a group on each side; marginal setae minute and cylindrical......................... Neoplatylecanium - Ventral tubular ducts absent; each stigmatic cleft with stigmatic spines normally distributed; marginal setae spinose...... 13 13(12) Claws each with denticle on widest part; each stigmatic cleft with stigmatic spines grouped in a triangle at base, numbering 9‒14; dorsal tubercles absent................................................................ Melanesicoccus - Claws each without a denticle on widest part; each stigmatic cleft containing 3 stigmatic spines; dorsal tubercles present submarginally.................................................................................. Neosaissetia

Bambusaecoccus maolanensis Meng & Xing sp. n. Material examined: Holotype: adult ♀, CHINA: Guizhou Prov., / Libo County, Yongkang Town, / 25°28′73″N, 107º94′15″E, / 707 m altitude, / on Dendrocalamopsis sp. (Bambusoideae), / 19. August. 2021, / Shitao Meng leg., mounted singly on a slide (GUGC). Paratypes: Same collection data as holotype, 8 adult ♀♀, 4 adult ♂♂, mounted singly on slides (GUGC). The slide lables are written in English. Adult female Appearance in life (Figs 1A–D): Body of adult female oval, mildly convex, 2.3‒3.5 mm long, 1.8‒2.3 mm wide; entire dorsum yellowish-brown, mediodorsally with a greyish brown longitudinal ridge, submargin with a quite wide, dark yellowish brown strip, without visible wax except for a small area of white wax near each stigmatic cleft. Slide-mounted adult female (n=9) (Figs 2, 3): Body broadly oval, 2.5‒3.7 (2.8) mm long, 2.0‒2.5 (2.3) mm wide. Stigmatic clefts deep and very pronounced, each reniform. Anal cleft approximately 1/4 of body length without sides fused. Dorsum. Derm membranous, lightly sclerotized in more mature specimens, with abundant small areolations that are more obvious in mature specimens; each areolation contains a central dorsal microductule. A narrow, strongly sclerotized area present around anal plates. Dorsal setae all spinose, each 7‒10 (8) μm long, sparsely distributed throughout but frequent around each stigmatic cleft. Dorsal pores of 2 types: (i) small convex, closed pores, each about 3 μm wide and (ii) small microducts each with a narrow outer ductule about 4 μm long, an inner ductule 6 μm long and swollen at proximal end, and sclerotized pore about 1.5‒2.0 (1.6) μm wide. Preopercular pores each about 4‒6 (5) μm wide, forming 2 compact groups, each of 60‒85 pores, situated anterolaterally to anterior margin of anal plates. Anal plates each 190‒210 (195) μm long, combined width 170‒180 (173) μm; each plate with 4 setae, with 3 along outer submargin and 1 near inner margin. Ano-genital fold with 2 pairs of short setae present along anterior margin and 3 or 4 pairs of longer setae laterally. Anal ring bearing 4 pairs of setae, each about 100 μm long, ring apparently with pores; anal tube quite short, anal ring lying beneath anal plates. Eyespots present. Margin. Marginal setae short and spinose, located on ventral surface apart from a few on dorsum on either side of each stigmatic cleft, each seta 11‒16 (13) μm long. Each side of body with 15‒20 marginal setae between anterior and posterior stigmatic clefts. Stigmatic clefts deep, with a narrow opening marginally, but widening submarginally, each with 20 stigmatic spines on dorsal surface; stigmatic spines variable in size, each 5‒14 μm long; each stigmatic cleft with inner margin sclerotized, and a small area of dorsal sclerotisation by inner margin, containing about 25 spiracular disc-pores. Venter. Derm entirely membranous. Ventral microducts distributed evenly on venter Multilocular disc-pores present, mostly each 7‒10 (8) μm wide, with mainly 5 or 6 (a few with 7 or 8) loculi, restricted to a small group of 20‒30 on each side at anterior end of anal cleft, posterior to genital opening. Spiracular disc-pores each with 5 loculi, present in a wide band between each spiracle and margin, with about 45‒55 pores in each anterior band and 50‒70 in each posterior band. Tubular ducts all of 1 type, each duct with a long, narrow outer ductule about 12 μm long, and a narrow inner ductule about 10 μm long, restricted to a small group of 15‒20 (total) on either side of genital opening. Setose setae abundant; pregenital setae with 4 setae on either side of anal opening (segment VII); a group of about 16 on each side of segment VI; about 23 on each side of V; and 10 or 11 on each side of each of segments IV and III; and 0 on segment II; also, each middle and hind leg with an adjacent group of 10‒15 setae. Antennae reduced, each about 130‒135 (132) μm long, with 7 ring-like segments; scape with 3 setae; pedicel with 2 setae; segment III with 3 setae; segment with 2 setae, 1 long and 1 short; V and IV each with 1 fleshy seta + 1 hair-like seta; VII with 3 hair-like setae and 3 stiff setae. Mouthparts rather large; clypeolabral shield about 265‒310 (272) μm long with 2 pairs of setae; labium shorter than clypeus, with 4 pairs of setae. Peritremes of anterior spiracles each about 95‒100 (96) μm wide, with 140–150 disc-pores; and those of posterior spiracles each about 98‒103 (101) μm wide, with 145–155 disc-pores. Legs reduced but each with a large coxal apodeme; segmentation difficult to discern; each tibia and tarsus very short, with 1 short seta; tarsal and claw digitules capitate, each 5‒7 μm long; claw about 20‒23 (21) μm long, without a denticle. Vulva not visible but probably situated between abdominal segments VI and VII. Remarks: Bambusaecoccus maolanensis sp. n. is the only species currently known in the genus. The morphology of the adult female is similar to that of Takahashilecanium rotundum (Takahashi, 1951), sharing the following character states: (i) stigmatic clefts present; (ii) spiracular disc-pores present in broad bands between margin and spiracles; (iii) preopercular pores present in two groups located laterad to anal plates; (iv) anal ring with four pairs of setae; and (v) pregenital disc pores forming a small group posterior to vulvar opening on each side of the anal cleft. Bambusaecoccus maolanensis can be distinguished from Takahashilecanium by (character states of T. rotundum in brackets): (i) stigmatic clefts each associated with about 20 dorsal stigmatic spines (each cleft containing only 3 stigmatic spines); (ii) ventral tubular ducts present in a small group on each side of genital opening (ventral tubular ducts absent); and (iii) legs and antennae reduced (legs and antennae well developed); and (iv) presence of a group of 10‒15 setae on venter just mesad to each middle and hind leg (absent). Ecological note: Specimens of B. maolanensis were found under carton coverings made by the ant Crematogaster subnuda nigrosubnuda Özdikmen 2010 (Hymenoptera: Formicidae: Myrmicinae) on stem nodes of bamboo, Bambusa (Dendrocalamopsis) sp. (Poaceae: Bambusoideae) (Figs 4A–B). The ants were feeding on the honeydew eliminated by the scale insects and had built a tent-like carton cover to protect them from predators and parasites. Both female and male scales of various developmental stages were usually found together. Adult male Appearance in life (Figs 5A–D): Body yellowish-brown. Genital segments uncinate, about 1/5th total body length; antennae rather short, each approximately half total body length; wing petaliform, about 3/5th total body length. Slide-mounted adult male (Figs 6, 7): Body 1.84–1.89 mm long, with hair-like setae (hs) and fleshy setae (fs), mainly restricted to the limbs. Antennae rather short, each about half total body length. Head with two pairs of simple eyes. Procoxae each with 1 pair long hair-like seta. Caudal extension of abdominal segment VIII rounded, with mild sclerotisation and moderate protuberance. Glandular pouches numbering 1 pair. Fore wings each slightly shorter than total body length. Head. Roughly diamond-shaped, 216–220 μm long and about 234 μm wide. Median crest (mc) well developed, with blurry reticulations. Postoccipital ridge (por) absent. Mid-cranial ridge (vmcr) narrow but clear. Preocular ridge (procr) present ventrally, extending posteriorly. Genae (g) large and membranous, without genal setae (gs) and without polygonal reticulations but with a few striations. Eyes: with 2 pairs of round simple eyes, 1 pair dorsal (dse) and 1 pair ventral (vse), subequal in size, each 40–45 μm in diameter. Ocelli (o) present laterally. Ocular sclerite (ocs) sclerotized and reticulated, each reticulation containing microridges. Postocular ridge (pocr) dorsally extending medially to median crest (dividing around each ocellus). Dorsal ocular setae absent, but with a small seta between postocular ridge (pocr) and median crest (mc). Cranial apophysis (ca) present. Antennae each 10 segmented and filiform. Segment lengths in μm: scape (scp) 31‒35, 45–49 wide, with 3 hs; pedicel (pdc) 45–50 long, 50–52 wide, with 2 or 3 hs on ventral surface and campaniform pore present. Segments III–X each 28‒33 wide; length of fs 17–19 (occasionally down to 12); segment lengths: III 60–65; IV 110–115; V 135–140; VI 124–129; VII 113–118; VIII 105–110; IX 88–93; X 66–71; approximate number of setae per segment: III, 6 or 7 fs + 0 hs; IV, 10–16 fs + 0 hs; V–VII, 16–25 fs + 0 hs; VIII and IX, 13–17 fs + 3 hs; segment X with 16–19 fs, of which 5 probably antennal bristles (ab) but not differentiated + 3 capitate setae (caps). Prothorax. Pronotal ridge (prnr) well developed, apparently fused medially. Pronotal sclerite (prn) wide, without lateral pronotal setae. Post-tergites (pt) present, without post-tergital setae. Median pronotal and other dorsal and pleural setae absent. Proepisternum + cervical sclerite (pepcv) well developed. Sternum (stn 1) with strong, bow-shaped, transverse ridge. Median ridge absent but with a broad striated area in this position. Prosternal setae, anteprosternal setae and antemesospiracular setae absent. Mesothorax. Prescutum (prsc) slightly wider than long, 100–105 μm long and 190–195 μm wide. Prescutal setae (prscs) absent. Prescutal ridge (pscr) and prescutal suture (pscs) well developed. Median membranous area (sma) 125–130 μm long and 190–195 μm wide. Scutum margin with a small group of blurry reticulations. Scutal setae (scts) absent. Scutellum (scl) 165–170 μm long and 265–270 μm wide, with a moderately large foramen; scutellar setae absent. Mesepisternum (eps 2) with petaliform nodules. Postalare (pa) striated anteriorly, without postalare setae. Mesosternum (stn 2) large, about 180–190 μm long and 270–275 μm wide; stn 2 bounded anteriorly with strong marginal ridges (mr) and posteriorly with strong precoxal ridges (pcr 2), without mesosternal setae (stn 2 s). Median ridge (mdr) well developed and complete. Lateropleurite (lpl) without marginal ridge. Furca (f) well developed but short, extending anteriorly. Subepisternal ridge (ser) well developed. Postmesospiracular setae absent. Mesothoracic spiracle (sp 2) peritreme 37–39 μm wide. Antemetaspiracular setae absent. Mesopostnotum (pn 2) developed normally. Tegula (teg) without tegular setae (tegs). Metathorax. Metapostnotum (pn 3) absent. Dorsal and ventral parts of metapleural ridge (plr 3) well developed. Metepisternum (eps 3) lightly sclerotized. Metepimeron (epm 3) long and without setae. Metathoracic spiracle (sp 3) peritreme 37‒39 μm wide. Metasternum (stn 3) membranous; posterior metasternal setae absent. Wings. Fore wings hyaline, 1.13–1.18 mm long and about 0.58 mm wide (ratio of length to width 1:0.5). alar setae and alar sensoria absent. Hamulohalteres absent. Legs. Metathoracic legs marginally longest. All leg segments with setae, mainly fs. Coxa (cx) lengths (μm): I, 107; II, 100; and III, 100–105, each procoxa bearing 2 long hair-like setae, each 25‒30 μm long, and 8–10 fs + 3 hs. Metacoxa with 12–15 fs + 7 hs. Trochanterofemora (tfm) with segmentation indistinct, lengths (μm): I, 295–300, II, 270–275, III, 305–310. Metatrochanter with 20–25 fs + 8 hs. Tibiae (ti) long, lengths (μm): I, 330–335; II, 350–355, and III, 400–405. Metatibia with 40–50 fs + 14 hs. Apical spurs (tibs) on tibiae each about 26 μm long. Tarsi (ta) one segmented, I, II and III each 100–110 μm long. Metatarsi each with 10–15 fs + 14 hs. Distal tarsal spur (tars) present, each 25–28 μm long. Tarsal digitules (tdt) slightly longer than claw. Claws (c) short, each about 60‒65 μm long and without denticle (cd). Claw digitules (cdt) with small capitate apices and slightly shorter than claw. Abdomen. Segments I–VIII: tergites on segments IV–VIII (at) with light sclerotisation. Abdominal sternites (as) slightly sclerotized. Segment VII with caudal extensions. Dorsal abdominal setae (ads) absent. Segment VIII with 2 ante-anal setae (aas) each 15–17 μm long. Pleural setae all hs. Dorsal pleural setae (dpls): segments I–III each with 0, III‒VII each with 6, VIII with 5. Ventral pleural setae (vpls) absent. Ventral abdominal setae hair-like; each side of segments I and II each with 1 seta, segments VI‒VIII each with 1 seta, and segments III‒V with 2 setae each. Glandular pouches (gp) deep, each divided into inner and outer sections; each pouch containing small pores and 2 glandular pouch setae (gls), these proportionately rather short, each 90‒95 μm long. Genital segments. Segment IX intimately fused onto caudal segment. Penial sheath (ps) 355–360 μm long and 55–60 μm wide at base, about 1/5th total body length (ratio of total body length to penial sheath length 1:0.19), with slightly sclerotized margins. Basal rod (bra) very short, 15–20 μm long, its anterior not approaching basal membranous area (bma). Aedeagus (aed) 90–95 μm long, apex of penial sheath with a membranous extension, bearing minute setae, each about 3‒5 μm long setae (gts). Posterior and dorsal margins of penial sheath all with a cluster of small sensillae (gtp) near apex. Remarks: The male of B. maolanensis shows some similarities to that of Cribropulvinaria tailungensis Hodgson & Martin 2001, sharing the following character states: (i) sternum (stn 1) with a strong, bow-shaped, transverse ridge; (ii) scutum with a few polygonal nodulations laterad to scutellum; (iii) hamulohalteres absent and (iv) the presence of distinct sclerotized tergal plates on segments II to VIII; and (v) glandular pouches (gp) present, each with 2 setae. The male of B. maolanensis can be distinguished from that of C. tailungensis (characteristics of C. tailungensis in brackets) by possessing: (i) genae (g) with a few striations (genae without striations or polygonal reticulations); (ii) abdominal ventral setae present (abdominal ventral setae absent); and (iii) episternum (eps 1) slightly sclerotized and without postmetaspiracular setae (pmss) (episternum (eps 1) sclerotized, with fs postmetaspiracular setae (pmss) present). Etymology: The specific name maolanensis is composed of maolan, the name of the site in Libo where this species was collected, and - ensis (Latin), a suffix denoting place or locality., Published as part of Meng, Shitao & Xing, Jichun, 2022, Bambusaecoccus maolanensis, a new soft scale genus and species from China (Hemiptera: Coccomorpha: Coccidae), pp. 419-430 in Zootaxa 5168 (4) on pages 422-429, DOI: 10.11646/zootaxa.5168.4.2, http://zenodo.org/record/6899711, {"references":["Ozdikmen, H. (2010) New names for some preoccupied specific and subspecific epithets in the family Formicidae (Hymenoptera). Munis Entomology and Zoology, 5 (supplement), 986 - 1000.","Hodgson, C. J. & Martin, J. H. (2001) Three noteworthy scale insects (Hemiptera: Coccoidea) from Hong Kong and Singapore, including Cribropulvinaria tailungensis, new genus and species (Coccidae), and the status of the cycad-feeding Aulacaspis yasumatsui (Diaspididae). The Raffles Bulletin of Zoology, 49, 227 - 250."]}

Yao, Binbin, Xing, Jichun (2022): New replacement name for the genus Kayania Medrano, Kury & Mendes, 2021 (Arachnida: Opiliones: Cosmetidae). Zootaxa 5155 (3): 449-450, DOI: https://doi.org/10.11646/zootaxa.5155.3.9

similis Dai, Viraktamath & Zhang, 2010 Distribution: China (Zhejiang, Hunan, Gansu); Japan., Published as part of Cao, Wenjun & Xing, Jichun, 2022, Japananoides, a new leafhopper genus from China (Hemiptera: Cicadellidae: Deltocephalinae), pp. 345-354 in Zootaxa 5154 (3) on page 346, DOI: 10.11646/zootaxa.5154.3.7, http://zenodo.org/record/6644812, {"references":["Dai, W., Viraktamath, C. A. & Zhang, Y. L. (2010 b) A review of the leafhopper genus Hishimonoides Ishihara (Hemiptera: Cicadellidae: Deltocephalinae). Zoological science, 27 (9), 771 - 781. https: // doi. org / 10.2108 / zsj. 27.771"]}

fodingensis Xing, Dai & Li, 2010 Distribution: China (Guizhou)., Published as part of Cao, Wenjun & Xing, Jichun, 2022, Japananoides, a new leafhopper genus from China (Hemiptera: Cicadellidae: Deltocephalinae), pp. 345-354 in Zootaxa 5154 (3) on page 346, DOI: 10.11646/zootaxa.5154.3.7, http://zenodo.org/record/6644812

hamuleus Du & Dai, 2019 Distribution: China (Guangxi).

aberrans Knight, 1970 Distribution: China (Hainan, Taiwan); Borneo; Malaysia; Singapore; Sri Lanka., Published as part of Cao, Wenjun & Xing, Jichun, 2022, Japananoides, a new leafhopper genus from China (Hemiptera: Cicadellidae: Deltocephalinae), pp. 345-354 in Zootaxa 5154 (3) on page 346, DOI: 10.11646/zootaxa.5154.3.7, http://zenodo.org/record/6644812

sellatus (Uhler, 1896) Distribution: China (Anhui, Fujian, Guizhou, Henan, Hongkong, Hubei, Hunan, Jiangsu, Jiangxi, Liaoning, Ningxia, Shandong, Shaanxi, Shanxi, Sichuan, Taiwan, Xinjiang, Zhejiang); Afghanistan; Armenia; Australia; Ethiopia; Georgia; India; Indonesia; Japan; Korea; Malaysia; Papua New Guinea; Philippines; Russia; Sri Lanka; Tanzania., Published as part of Cao, Wenjun & Xing, Jichun, 2022, Japananoides, a new leafhopper genus from China (Hemiptera: Cicadellidae: Deltocephalinae), pp. 345-354 in Zootaxa 5154 (3) on page 347, DOI: 10.11646/zootaxa.5154.3.7, http://zenodo.org/record/6644812, {"references":["Uhler, P. R. (1896) Summary of the Hemiptera of Japan presented to the United States National Museum by Professor Mitzukuri. Proceedings of the United States National Museum, 19, 255 - 297. https: // doi. org / 10.5479 / si. 00963801.1108.255"]}

recurvatis Li, 1988 Distribution: China (Guizhou, Gansu, Henan, Shaanxi, Hubei, Sichuan, Yunnan)., Published as part of Cao, Wenjun & Xing, Jichun, 2022, Japananoides, a new leafhopper genus from China (Hemiptera: Cicadellidae: Deltocephalinae), pp. 345-354 in Zootaxa 5154 (3) on page 346, DOI: 10.11646/zootaxa.5154.3.7, http://zenodo.org/record/6644812

diffractus Dai, Fletcher & Zhang, 2013 Distribution: China (Jiangxi); Australia; Thailand., Published as part of Cao, Wenjun & Xing, Jichun, 2022, Japananoides, a new leafhopper genus from China (Hemiptera: Cicadellidae: Deltocephalinae), pp. 345-354 in Zootaxa 5154 (3) on page 346, DOI: 10.11646/zootaxa.5154.3.7, http://zenodo.org/record/6644812, {"references":["Dai, W., Fletcher, M. J. & Zhang, Y. L. (2013) First records of the genus Hishimonus Ishihara from Thailand (Hemiptera: Cicadellidae: Deltocephalinae: Opsiini) including description of three new species. Zootaxa, 367 (3), 301 - 316. https: // doi. org / 10.11646 / zootaxa. 3670.3.1"]}

Opsius tigripes (Lethierry, 1876) Distribution: China (Xinjiang, Neimenggu, Hebei, Gansu); Afghanistan; European Russia; Iran; Saudi Arabia., Published as part of Cao, Wenjun & Xing, Jichun, 2022, Japananoides, a new leafhopper genus from China (Hemiptera: Cicadellidae: Deltocephalinae), pp. 345-354 in Zootaxa 5154 (3) on page 348, DOI: 10.11646/zootaxa.5154.3.7, http://zenodo.org/record/6644812, {"references":["Lethierry, L. F. (1876) Homopteres nouveaux d'Europe et des contres voisines. Compte rendu des seances de la Societe Entomologique de Belgique, 19, 5 - 17."]}