taxonID	type	description	language	source
316487FCFFEFFFCDFC354803FA6B9D0E.taxon	materials_examined	Type genus Aluntia Stål, 1866. Diagnosis The tribe can be distinguished by the following combination of characters: vertex with posterior margin	en	Song, Zhi-Shun, Szwedo, Jacek, Wang, Rong-Rong, Liang, Ai-Ping (2016): Systematic revision of Aluntiini Emeljanov, 1979 (Hemiptera: Fulgoromorpha: Dictyopharidae: Dictyopharinae): reclassification, phylogenetic analysis, and biogeography. Zoological Journal of the Linnean Society 176 (2): 349-398, DOI: 10.1111/zoj.12319, URL: http://dx.doi.org/10.1111/zoj.12319
316487FCFFE7FFC5FF6F4B5BFA6A9D0E.taxon	description	Synonymized under Aluntia Stål, 1866 by Distant 1906: 237 and here resurrected. Type species	en	Song, Zhi-Shun, Szwedo, Jacek, Wang, Rong-Rong, Liang, Ai-Ping (2016): Systematic revision of Aluntiini Emeljanov, 1979 (Hemiptera: Fulgoromorpha: Dictyopharidae: Dictyopharinae): reclassification, phylogenetic analysis, and biogeography. Zoological Journal of the Linnean Society 176 (2): 349-398, DOI: 10.1111/zoj.12319, URL: http://dx.doi.org/10.1111/zoj.12319
316487FCFFE7FFC5FF6F4B5BFA6A9D0E.taxon	diagnosis	Diagnosis The genus can be separated from other Aluntiini genera by the following combination of characters: frons with intermediate carinae weakly ridged, median carina incomplete, absent in middle; tegmina somewhat trun- cate apically, with numerous dendroid nodose veins; Sc + R and M branched before CuA at basal one-third; apical area densely covered with transverse veins; costal cell distinctly broad, with dendroid nodose veins in entire area; and aedeagus with a pair of slender, elongate, sclerotized endosomal processes. Redescription Body distinctly large and robust. General colour ochraceous in dead specimens (probably viridescent or stramineous green in life). Head (Figs 7 A – C, 9 A – C) as long as or a little longer than pronotum and mesonotum combined. Cephalic process (Figs 7 B, 9 B) more or less compressed dorsoventrally. Vertex (Figs 7 A, 9 A) with median carina absent, only median furrowed suture visible between eyes; lateral carinae ridged, nearly parallel, relatively broad and flat towards apex; anterior margin angulately convex at ∼ 90 °, posterior margin indistinct, sloped down into the pronotum. Frons (Figs 7 C, 9 C) with intermediate carinae converging posteriorly and extending before compound eyes; median carina incomplete, distinct at apex and base, absent in middle. Rostrum, eyes, ocelli, and antennae similar to Aluntia. Pronotum and mesonotum (Figs 7 C, 9 C) similar to Aluntia, but mesonotum with lateral carinae more or less curved outwards. Tegmina (Fig. 2 C) transparent, large, and broad, nearly 2.4 – 2.5 times as long as broad; apex somewhat truncate; anterior margin distinctly expanded into broad sclerotized costal area; basal twothirds to four-fifths with dendroid veins densely interspersed among longitudinal veins; Sc + R and M branched before CuA at basal one-third; M 3 + 4 bifurcating M 3 and M 4 not beyond the middle; Sc + R, M, and CuA branching into accessory veins successively four times; apical area densely covered with transverse veins, with 21 – 25 apical cells; costal cell distinctly broad, with numerous dendroid veins in entire area. Legs similar to Aluntia. Male genitalia with pygofer similar to Aluntia, in lateral view posterior margin more or less projecting near upper middle (Figs 7 E, 9 E), in dorsal view	en	Song, Zhi-Shun, Szwedo, Jacek, Wang, Rong-Rong, Liang, Ai-Ping (2016): Systematic revision of Aluntiini Emeljanov, 1979 (Hemiptera: Fulgoromorpha: Dictyopharidae: Dictyopharinae): reclassification, phylogenetic analysis, and biogeography. Zoological Journal of the Linnean Society 176 (2): 349-398, DOI: 10.1111/zoj.12319, URL: http://dx.doi.org/10.1111/zoj.12319
316487FCFFE3FFDEFC804936FD029F6F.taxon	description	(FIGS 1 G, 9 A – J)	en	Song, Zhi-Shun, Szwedo, Jacek, Wang, Rong-Rong, Liang, Ai-Ping (2016): Systematic revision of Aluntiini Emeljanov, 1979 (Hemiptera: Fulgoromorpha: Dictyopharidae: Dictyopharinae): reclassification, phylogenetic analysis, and biogeography. Zoological Journal of the Linnean Society 176 (2): 349-398, DOI: 10.1111/zoj.12319, URL: http://dx.doi.org/10.1111/zoj.12319
316487FCFFE3FFDEFC804936FD029F6F.taxon	description	Redescription BL, ♂ 14.8 – 16.6 mm; HL, ♂ 4.5 – 4.9 mm; HW, ♂ 1.1 – 1.2 mm; TL, ♂ 9.4 – 10.5 mm. Head (Fig. 9 A – C) elongate, 1.2 – 1.3 times as long as pronotum and mesonotum combined. Tegmina nearly 2.4 times as long as broad; basal four-fifths with dendroid veins dense. Male genitalia with pygofer with ratio of ventral to dorsal width ∼ 2.0: 1.0 in lateral view, posterior margin distinctly projecting near upper middle (Fig. 9 E). Gonostyles with apex bluntly rounded and strongly projecting backward; in lateral view upper margin with a large, broad, and blunt process near middle, direct- ed anteriorly (Fig. 9 F). Aedeagus with endosomal processes abruptly curved dorsolaterally in middle; phallobase with apex produced in two lamellar processes dorsally and ventrally, respectively: dorsal pair elongate and large (Fig. 9 H – J). Segment X in dorsal view oval, large, and broad, with ratio of length to width in middle ∼ 1.3: 1.0 (Fig. 9 G). Type material examined Syntype ♂, [Sri Lanka]: 2 – 86; 239; romosa [Melichar’s handwriting], det. Melichar; Aselgeia = Dendrophora [Melichar’s handwriting]; Aluntia romosa [Melichar’s handwriting]; Collection Dr. Melichar; Dendrophora ramosa sp. n. L. Melichar, 1903 [Lauterer’s handwriting], P. Lauterer det. 1991 (MMBC). Other material examined [Sri Lanka]: 1 ♂, Ceylon, E. Prov., Kuchchavell, 20 miles NW Trincomalee, 9 – 10. II. 1962, Loc. 60., Semi desert; 1 ♂, Ceylon, E. Prov., Madura Oya, 15 miles NNW Bibile, 13. III. 1962, Loc. 138., Swept on veg, by stream (both in MZLU, Lund University Ceylon Expedition 1962, Brinck-Andersson-Cederholm). Distribution Sri Lanka. Remarks Distant (1906) listed that D. ramosa was recorded from the Malay Peninsula, but his description probably represented a D. borneensis. Nast (1949) suggested that the record from the Malay Peninsula was wrong.	en	Song, Zhi-Shun, Szwedo, Jacek, Wang, Rong-Rong, Liang, Ai-Ping (2016): Systematic revision of Aluntiini Emeljanov, 1979 (Hemiptera: Fulgoromorpha: Dictyopharidae: Dictyopharinae): reclassification, phylogenetic analysis, and biogeography. Zoological Journal of the Linnean Society 176 (2): 349-398, DOI: 10.1111/zoj.12319, URL: http://dx.doi.org/10.1111/zoj.12319
316487FCFFFCFFDCFEB34B62FF399F78.taxon	materials_examined	Type species	en	Song, Zhi-Shun, Szwedo, Jacek, Wang, Rong-Rong, Liang, Ai-Ping (2016): Systematic revision of Aluntiini Emeljanov, 1979 (Hemiptera: Fulgoromorpha: Dictyopharidae: Dictyopharinae): reclassification, phylogenetic analysis, and biogeography. Zoological Journal of the Linnean Society 176 (2): 349-398, DOI: 10.1111/zoj.12319, URL: http://dx.doi.org/10.1111/zoj.12319
316487FCFFFCFFDCFEB34B62FF399F78.taxon	diagnosis	Diagnosis The genus may be distinguished by the following combination of characters: cephalic process distinctly compressed dorsoventrally, flat and narrowing from base to apex; frons with intermediate carinae strongly elevated, median carina complete, strongly elevated at apex, and slightly keeled in middle; tegmina distinctly elongate, without dendroid secondary veins; Cu branched before Sc + R and M; costal cell with suboblique veins on apical one-third; male pygofer with an obtuse posterior process; and aedeagus with a pair of elongate, large, strongly inflated, and membranous endosomal processes. Diversity and distribution Dictyomorpha includes seven species and exhibits an Austro-Oriental distribution. Remarks This genus was recently revised by Liang & Song (2012). Six species, except for Dictyomorpha hectica Haupt, 1926, were described and illustrated, along with fifthinstar nymph and wax glands of parts of Dictyomorpha species.	en	Song, Zhi-Shun, Szwedo, Jacek, Wang, Rong-Rong, Liang, Ai-Ping (2016): Systematic revision of Aluntiini Emeljanov, 1979 (Hemiptera: Fulgoromorpha: Dictyopharidae: Dictyopharinae): reclassification, phylogenetic analysis, and biogeography. Zoological Journal of the Linnean Society 176 (2): 349-398, DOI: 10.1111/zoj.12319, URL: http://dx.doi.org/10.1111/zoj.12319
316487FCFFFCFFDCFEB34B62FF399F78.taxon	description	Redescription Body relatively small. General colour ochraceous in dead specimens (probably viridescent or stramineous green in life). BL, ♂ 16.9 mm, ♀ 18.6 mm; HL, ♂ 5.4 mm, ♀ 5.7 mm; HW, ♂ 1.1 mm, ♀ 1.2 mm; TL, ♂ 10.5 mm, ♀ 12.3 mm. Cephalic process (Fig. 10 A – C) 1.9 times as long as pronotum and mesonotum combined. Vertex (Fig. 10 A) with median carina distinct only at extreme apical part and basal one-fifth, rest of carina indistinct and sometimes slightly sutured. Frons (Fig. 10 C) with intermediate carinae strongly elevated and blade-like, converging at eye level; median carina complete. Tegmina elongate and slender, nearly 3.5 times as long as broad; costal cell with between six and eight suboblique veins. Male genitalia with pygofer relatively large and broad, with ratio of ventral to dorsal width ∼ 1.4: 1.0, in lateral view posterior margin distinctly produced posteriorly near middle, with posteriorly produced part obtuse apically (Fig. 10 E); in dorsal view dorsal margin excavated to accommodate segment X, dorsolateral margins strongly produced posteriorly (Fig. 10 F). Gonostyles symmetrical; base narrow, expanded towards middle, then gradually narrowed towards apex; apex bluntly rounded; upper process large and blunt, directed dorsally (Fig. 10 E). Aedeagus (Fig. 10 G – I) with endosomal processes extended from phallotheca: in lateral view apical half membranous and inflated, turned dorsoposteriorly; relatively short, small, and slender, apex acute; phallobase relatively narrow and elongate, phallobase with two membranous lobes ventrally. Segment X in dorsal view with ratio of length to width in middle ∼ 2.1: 1.0 (Fig. 10 F). Type material examined Paratype ♀, [Philippines]: Mt. Banahao, Luzon, IV. 1923, Dictyomorpha hectica Hpt. [Haupt’s handwriting], Paratypoid [red label], ♀, Dictyomorpha hectica Haupt, 1926, des. R. Remane 2003 (SNSD). Other material examined [Philippines]: 1 ♂, Mt. Banahao, P. I., Baker; Dictyomorpha elongata Mel. [Melichar’s handwriting], det. Melichar; Cotypus [red label]; Collection Dr. Melichar; Dictyomorpha elongata Melichar, 1903, ♂, Melichar det. 1912 [Lauterer’s handwriting] (MMBC); 1 nymph, Los Banos, P. I., IX. 1915 (BPBM). Distribution Philippines (Luzon, Los Banos). Remarks Liang & Song (2012) did not examine the type and other adult material of D. hectica except for a nymph from Los Banos, Luzon, Philippines, which is adjacent to the type locality. One male specimen from Mt. Banahao, Philippines, deposited in MMBC was determined as D. elongata by Melichar and designated as a co-type of D. elongata by Lauterer. In fact, Mt. Banahao was not recorded in Melichar’s dictyopharid monograph (Melichar, 1912: 104); hence, the designation for D. elongata is rejected here. We redescribe this species and add the description of male genitalia for the first time.	en	Song, Zhi-Shun, Szwedo, Jacek, Wang, Rong-Rong, Liang, Ai-Ping (2016): Systematic revision of Aluntiini Emeljanov, 1979 (Hemiptera: Fulgoromorpha: Dictyopharidae: Dictyopharinae): reclassification, phylogenetic analysis, and biogeography. Zoological Journal of the Linnean Society 176 (2): 349-398, DOI: 10.1111/zoj.12319, URL: http://dx.doi.org/10.1111/zoj.12319
316487FCFFFEFFDCFF594B44FC089B16.taxon	materials_examined	Type species	en	Song, Zhi-Shun, Szwedo, Jacek, Wang, Rong-Rong, Liang, Ai-Ping (2016): Systematic revision of Aluntiini Emeljanov, 1979 (Hemiptera: Fulgoromorpha: Dictyopharidae: Dictyopharinae): reclassification, phylogenetic analysis, and biogeography. Zoological Journal of the Linnean Society 176 (2): 349-398, DOI: 10.1111/zoj.12319, URL: http://dx.doi.org/10.1111/zoj.12319
316487FCFFFEFFDCFF594B44FC089B16.taxon	diagnosis	Diagnosis The genus can be separated from other Aluntiini genera by the following combination of characters: cephalic process nearly 1.3 times as long as pronotum and mesonotum combined; vertex with median carina only visible basally; frons with lateral and median carinae strongly ridged and blade-like; tegmina without dendroid secondary veins; ten suboblique veins on costal cell from basal one-third to apex; and aedeagus with a pair of spinous, sclerotized, black-tipped, and not inflated endosomal processes. Diversity and distribution Indodictyophara is a monotypic genus known only from southern India.	en	Song, Zhi-Shun, Szwedo, Jacek, Wang, Rong-Rong, Liang, Ai-Ping (2016): Systematic revision of Aluntiini Emeljanov, 1979 (Hemiptera: Fulgoromorpha: Dictyopharidae: Dictyopharinae): reclassification, phylogenetic analysis, and biogeography. Zoological Journal of the Linnean Society 176 (2): 349-398, DOI: 10.1111/zoj.12319, URL: http://dx.doi.org/10.1111/zoj.12319
316487FCFFFEFFDCFCC74F89FA479D0E.taxon	materials_examined	Type species Madagascaritia angusta Song & Liang sp. nov., by present designation. Diagnosis This new genus can be separated from other Aluntiini genera by the following combination of characters: cephalic process with dorsal surface very narrow and compressed laterally before the eyes, so it becomes nearly triangular in cross section; frons with intermediate carinae strongly elevated, median carina incomplete or complete but obscure in middle; tegmina with costal cell distinctly narrow, coriaceous, opaque, and bright yellow, with suboblique veins (although observed with difficulty because of sclerotic surface), without dendroid secondary veins; basal three-quarters with dendroid nodose secondary veins densely interspersed among longitudinal veins; Sc + R, M, and CuA first branching nearly abreast. Description General colour ochraceous in dead specimens (probably viridescent or stramineous green in life). Head (Fig. 11 A – C) distinctly elongate, 1.5 – 1.8 times as long as pronotum and mesonotum combined. Cephalic process with dorsal surface very narrow and compressed laterally before the eyes in dorsal view (Fig. 11 A), so it becomes nearly triangular in cross section. Vertex (Fig. 11 A) with median carina absent, only median furrowed suture visible; lateral carinae strongly ridged, convergent anteriorly between eyes, slightly sinuate in front of eyes, and then narrowed and nearly subparallel towards apex, but apex acuate; posterior margin weakly ridged, arcuately concave. Frons (Fig. 11 C) with lateral carinae narrow and elongate; intermediate carinae strongly elevated, converging posteriorly and extending before eyes; median carina incomplete, or complete but obscure in middle. Clypeus, rostrum, eyes, ocelli, and antennae similar to Aluntia. Pronotum and mesonotum (Fig. 11 A) similar to Aluntia. Tegmina (Fig. 2 F) elongate and broad, translucent, and dull whitish, nearly 2.5 times as long as broad; costal cell very narrow, mostly coriaceous, opaque, and bright yellow in colour, with suboblique veins (although observed with difficulty because of sclerotic surface), without dendroid secondary veins; apex rounded; basal two-thirds with dendroid nodose	en	Song, Zhi-Shun, Szwedo, Jacek, Wang, Rong-Rong, Liang, Ai-Ping (2016): Systematic revision of Aluntiini Emeljanov, 1979 (Hemiptera: Fulgoromorpha: Dictyopharidae: Dictyopharinae): reclassification, phylogenetic analysis, and biogeography. Zoological Journal of the Linnean Society 176 (2): 349-398, DOI: 10.1111/zoj.12319, URL: http://dx.doi.org/10.1111/zoj.12319
316487FCFFFBFFD9FF0D4A0BFA6B9D0E.taxon	description	(FIGS 1 L, 2 F, 12 A – C)	en	Song, Zhi-Shun, Szwedo, Jacek, Wang, Rong-Rong, Liang, Ai-Ping (2016): Systematic revision of Aluntiini Emeljanov, 1979 (Hemiptera: Fulgoromorpha: Dictyopharidae: Dictyopharinae): reclassification, phylogenetic analysis, and biogeography. Zoological Journal of the Linnean Society 176 (2): 349-398, DOI: 10.1111/zoj.12319, URL: http://dx.doi.org/10.1111/zoj.12319
316487FCFFFBFFD9FF0D4A0BFA6B9D0E.taxon	description	Redescription Apex of head with a pair of irregular bronwnish black spots visible from above and beneath (Fig. 12 A, B); BL, ♀ 18.9 mm; HL, ♀ 5.6 mm; HW, ♀ 1.2 mm; TL, ♀ 11.1 mm. Head nearly 1.8 times as long as pronotum and mesonotum combined (Fig. 12 A). Tegmina (Fig. 2 F) with Sc + R, M, and CuA branching into accessory veins successively four times; apical margin with 24 cells. Female genitalia similar to Aluntia. Segment X relatively broad, base narrow, gradually expanded towards apex, with ratio of length to width at apex ∼ 1.8: 1.0. Male unknown. Type material examined Holotype ♀ (MIZ 313167), Madagascar: Périnet, 8. I. 1938; B. Kreczmer & A. Fiedler leg.; Type [red label]; Aluntia hova sp. nov. ♀, J. Nast, det. 1949 [Nast’s handwriting] (Mus. Zool. Polonicum, Warszawa, 12 / 45; MIZPAS). Distribution Madagascar. ARJUNINI SONG & SZWEDO TRIB. NOV. Type genus	en	Song, Zhi-Shun, Szwedo, Jacek, Wang, Rong-Rong, Liang, Ai-Ping (2016): Systematic revision of Aluntiini Emeljanov, 1979 (Hemiptera: Fulgoromorpha: Dictyopharidae: Dictyopharinae): reclassification, phylogenetic analysis, and biogeography. Zoological Journal of the Linnean Society 176 (2): 349-398, DOI: 10.1111/zoj.12319, URL: http://dx.doi.org/10.1111/zoj.12319
316487FCFFFBFFD9FF0D4A0BFA6B9D0E.taxon	diagnosis	Diagnosis This new tribe can be distinguished by the following combination of characters: clypeus distinctly elongate, extending to apex of middle coxae; rostrum distinctly elongate, beyond apex of hind femora; tegmina submacropterous and transparent, apical one-third not overlapping, apex somewhat pointed; corium without fold; veins with long setae, Sc + R and M veins on tegmina with a long common stem; claval suture extending to posterior margin; hindwings with anal area reduced, only a very small portion folded inwards, secondary fold absent; ACL of gonapophysis VIII with seven large teeth of varying sizes and shapes from base to apex; basal four teeth with base transversally prolonged and strongly ridged; and Gp 1 of gonoplacs with filmy edging, without sensory appendage. Diversity and distribution Arjunini includes eight species in two genera restrict- ed to the southern Sunda Islands and New Guinea only (Fig. 25). This group may be distributed widely in Wallacea, New Guinea, and the western Pacific, which	en	Song, Zhi-Shun, Szwedo, Jacek, Wang, Rong-Rong, Liang, Ai-Ping (2016): Systematic revision of Aluntiini Emeljanov, 1979 (Hemiptera: Fulgoromorpha: Dictyopharidae: Dictyopharinae): reclassification, phylogenetic analysis, and biogeography. Zoological Journal of the Linnean Society 176 (2): 349-398, DOI: 10.1111/zoj.12319, URL: http://dx.doi.org/10.1111/zoj.12319
316487FCFFFAFFD8FEC74C77FA449D0D.taxon	materials_examined	Type species	en	Song, Zhi-Shun, Szwedo, Jacek, Wang, Rong-Rong, Liang, Ai-Ping (2016): Systematic revision of Aluntiini Emeljanov, 1979 (Hemiptera: Fulgoromorpha: Dictyopharidae: Dictyopharinae): reclassification, phylogenetic analysis, and biogeography. Zoological Journal of the Linnean Society 176 (2): 349-398, DOI: 10.1111/zoj.12319, URL: http://dx.doi.org/10.1111/zoj.12319
316487FCFFFAFFD8FEC74C77FA449D0D.taxon	diagnosis	Diagnosis The genus can be distinguished by the following combination of characters: cephalic process curved downwards before eyes; vertex with a secondary longitudinal carina bifurcating from subapex of lateral carinae; frons with lateral carinae well developed from clypeus, but obscure and gradually disappearing anterad to eyes, only a pale trace extending forwards; intermediate carinae extending before eyes; median carina complete, robust, and strongly convex; and aedeagus with a pair of ventrolateral lobes twining around endosomal processes. Redescription Head (Fig. 14 A – I) moderately elongate, as long as or slightly longer than pronotum and mesonotum combined, and curved downwards before eyes. Vertex (Fig. 14 A, D, G) with lateral carinae distinctly thickened, gradually widened from base, widest before eyes, gradually narrowed towards subapex, then abruptly converging to apex; surface between lateral carinae more or less convex, median carina absent, a transverse depression present at widest area; apex acute; posteri- or margin weakly ridged, arcuately concave. Apex of cephalic process with sharp secondary longitudinal carina bifurcating from subapex of lateral carinae of vertex, extending to the dorsal branch of lateral carinae of frons forming areolets (lanceolate cells in Emeljanov, 2008: 311), then joining to apex of intermediate carinae of frons (Fig. 14 J, K). Frons (Fig. 14 C, F, I) widest below antennae, slightly constricted between eyes and narrowed forwards; lateral carinae well developed from clypeus, but obscure and gradually disappearing anterad to eyes, only a pale trace extending forwards (Fig. 14 B, J); a weak carina crossed areolets, sometimes too weak to be visible (Emeljanov, 2008); intermediate carinae converging posteriorly and extending before eyes; median carina complete, robust, and strongly convex. An apical median longitudinal carina between anterior margins of frons and vertex very sharp and convex (Fig. 14 K). Eyes nearly rounded, callus postocularis reduced, forming a triangular process projecting posteriorly. Antennae shifted backwards, pedicel globose, with ∼ 40 distinct sensory plaque organs distributed over the entire surface. Pronotum (Fig. 14 A, D, G) relatively large, longer than half of mesonotum; anterior margin centrally arcuately convex, lateral marginal areas straight and sloping, with two lateral carinae on each side; upper carinae narrower than the lower carinae, so in dorsal view the lower carinae are distinctly visible (Fig. 14 A, D, G); posterior margin broadly angularly concave; disc flat and tricarinate, median and intermediate carinae sharp and high, with a lateral pit on each side. Mesonotum (Fig. 14 A, D, G) transversely broad, short, flat, and tricarinate; lateral carinae weakly tortuous and abruptly incurved apically, slightly converging forwards. Tegmina (Fig. 2 G) nearly three times as long as broad; apical area with transverse veins sparse. Legs elongate and slender, fore and middle femora and tibiae distinctly elongate, hind tibiae more than twice as long as hind femora; fore and middle femora slightly thickened at apex, without spine; hind tibiae with four lateral spines and seven apical teeth; hind tarsomeres I and II with between eight and 13 apical teeth, respectively. Male genitalia with pygofer distinctly narrow and elongate, more than twice ventral width, distinctly wider ventrally than dorsally, in lateral view posterior margin more or less projecting near upper middle (Figs 15 B, 16 B, 17 B). Gonostyles symmetrical; base narrow, expanded towards middle, then gradually narrowed towards apex; apex bluntly rounded and projecting backwards; upper process elongate, obtuse, and compressed dorsoventrally (Figs 16 E, 17 E). Aedeagus (Figs 15 A, D, E, 16 A, F, G, 17 A, F, G) with a pair of slender and moderately long endosomal processes extended from phallotheca: pigmented, sclerotized, nearly straight, and obtuse apically; phallobase sclerotized and pigmented at base, with inflated membranous apical lobes, without spines; dorsal lobe directed posteriorly and two ventrolateral lobes twining around endosomal processes, directed laterally. Segment X in dorsal view long, oval, dorsal margin deeply excavated to accommodate anal style, with ratio of length to width at base	en	Song, Zhi-Shun, Szwedo, Jacek, Wang, Rong-Rong, Liang, Ai-Ping (2016): Systematic revision of Aluntiini Emeljanov, 1979 (Hemiptera: Fulgoromorpha: Dictyopharidae: Dictyopharinae): reclassification, phylogenetic analysis, and biogeography. Zoological Journal of the Linnean Society 176 (2): 349-398, DOI: 10.1111/zoj.12319, URL: http://dx.doi.org/10.1111/zoj.12319
316487FCFFF2FFD0FEEF4F89FAC999F0.taxon	materials_examined	Type species	en	Song, Zhi-Shun, Szwedo, Jacek, Wang, Rong-Rong, Liang, Ai-Ping (2016): Systematic revision of Aluntiini Emeljanov, 1979 (Hemiptera: Fulgoromorpha: Dictyopharidae: Dictyopharinae): reclassification, phylogenetic analysis, and biogeography. Zoological Journal of the Linnean Society 176 (2): 349-398, DOI: 10.1111/zoj.12319, URL: http://dx.doi.org/10.1111/zoj.12319
316487FCFFF2FFD0FEEF4F89FAC999F0.taxon	diagnosis	Diagnosis The genus can be distinguished from Arjuna by the following combination of characters: vertex with lateral carinae abruptly incurved before eyes and narrowed into half as wide, parallel forwards, then distinctly widened at subapex, angularly convex at apex; frons with intermediate carinae strongly ridged, nearly parallel and extending below antennae; median carina almost absent, only poorly marked below antennae. Diversity and distribution Pippax was erected by Emeljanov (2008) based on four new species: Pippax alboruber, Pippax bulbinaso, Pippax opilionoides, and Pippax vanstallei from Papua New Guinea. Remarks Emeljanov (2008) provided a key to the species of the genus. We here provide a first description of the male and female genitalia of P. opilionoides.	en	Song, Zhi-Shun, Szwedo, Jacek, Wang, Rong-Rong, Liang, Ai-Ping (2016): Systematic revision of Aluntiini Emeljanov, 1979 (Hemiptera: Fulgoromorpha: Dictyopharidae: Dictyopharinae): reclassification, phylogenetic analysis, and biogeography. Zoological Journal of the Linnean Society 176 (2): 349-398, DOI: 10.1111/zoj.12319, URL: http://dx.doi.org/10.1111/zoj.12319
316487FCFFF2FFD0FEEF4F89FAC999F0.taxon	description	Redescription BL, ♂ 5.8 – 6.5 mm, ♀ 6.6 mm; HL, ♂ 1.5 – 1.7 mm, ♀ 1.7 mm; HW, ♂ 0.8 – 0.9 mm, ♀ 0.9 mm; TL, ♂ 3.8 – 4.1 mm, ♀ 4.1 mm. Male genitalia with pygofer distinctly narrow and elongate, more than twice ventral width, distinctly wider ventrally than dorsally (∼ 3.0: 1.0), posterior margin more or less projecting near upper middle in lateral view (Fig. 20 B). Gonostyles (Fig. 20 C) symmetrical; base narrow, expanded towards middle, then gradually narrowed towards apex; in lateral view apex bluntly rounded and projecting backwards; upper process elongate, obtuse, and compressed dorsoventrally (Fig. 20 D). Aedeagus (Fig. 21 A, B) with a pair of slender and mod- erately long endosomal processes extended from phallotheca: pigmented, sclerotized, nearly straight, and obtuse apically; phallobase sclerotized and pigmented at base and laterally, the remainder membranous, without spines; dorsal area with a large and elongate lobe, acute apically, and directed dorsally; ventrolateral area with two narrow and elongate lobes, directed posteriorly. Segment X in dorsal view oval, with ratio of length to width at base ∼ 1.2: 1.0 (Fig. 20 A). Anal style elongate, beyond the apical ventral margin of segment X. Female genitalia (Fig. 21 C – F) similar to Arjuna. Material examined Papua New Guinea: 1 ♂, 1 ♀, Madang Province, Bundi (5 ° 45 ′ S, 145 ° 15 ′ E), 10 – 12. III. 1987, N. D. Penny; 1 ♂, So. Side Mt. Missim, 1000 m, 24. II. 1978, E. I. Schlinger (all in CAS); 1 ♂, Wau, Morobe Distr., Mt. Missim, 1800 m, Malaise Trap, 22. IV. 1966, Gressitt & Wilkes (BPBM). Distribution Papua New Guinea (Morobe and Madang).	en	Song, Zhi-Shun, Szwedo, Jacek, Wang, Rong-Rong, Liang, Ai-Ping (2016): Systematic revision of Aluntiini Emeljanov, 1979 (Hemiptera: Fulgoromorpha: Dictyopharidae: Dictyopharinae): reclassification, phylogenetic analysis, and biogeography. Zoological Journal of the Linnean Society 176 (2): 349-398, DOI: 10.1111/zoj.12319, URL: http://dx.doi.org/10.1111/zoj.12319
