identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
260C87D6FFCE781DFF63B812FC6A9C5E.text	260C87D6FFCE781DFF63B812FC6A9C5E.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Gorczyciana Wolski et Taszakowski 2023	<div><p>Genus: Gorczyciana Wolski et Taszakowski gen. nov.</p><p>Type species: Gorczyciana sulawesica Wolski et Taszakowski gen. nov., here designated.</p><p>Diagnosis. Easily recognized by the following set of characters: body relatively large (more than 4.5 mm); dorsum with characteristic vestiture composed of moderately dense, erect and suberect, thin, caliciform, and apically serrate setae (Figs 2E, H, I); antennomere I relatively long, about as long as head length, curved near base, with long, erect, thick, cylindrical, apically serrate bristles (Figs 1, 2A, D, F); antennomere II weakly arcuate (Figs 1, 2A); pronotal collar weakly separated from remainder of pronotum by shallow depression (Fig. 2E); pronotal calli strongly upraised, occupying most of pronotum (Figs 2G, H); lateral margin weakly elevated and strongly carinate (Figs 2C, H); hemelytral veins convex along entire length (Fig. 2A); embolium wide (Fig. 2A); vulvar area with strongly developed sclerotizations (Figs 3C–F); apex of gonapophyses 8 and 9 obtuse, without any teeth; gonapophyses 8 connected by delicate membrane along entire length, this membrane furnished with a thin, elongated sclerotization originating near base of gonapophyses 8 and terminating near apex (ss) (Figs 3D, E, H).</p><p>Description. Female. Macropterous. TEXTURE AND VESTITURE. Dorsum covered with characteristic vestiture composed of moderately dense, erect and suberect, thin, caliciform and apically serrate setae (Figs 2E, H, I). Head, pronotum, thoracic pleura, mesoscutum and scutellum with net-like sculpture comprised of microsetae (Figs 2E, G, H, I). Head. Eyes covered with vestiture similar to dorsum (Fig. 2E); antennomere I covered with fine, closely fitting setae and with several stiff, long, erect, apically serrate cylindrical bristles (Fig. 2D); antennomere II covered with fine, moderately dense setae; antennomeres III and IV missing in examined specimen. Thorax. Pronotum. Anterior angles each with single long, erect, thick, apically serrate bristle (Fig. 2E). Thoracic pleura. Covered with sparse, recumbent scale-like setae. Hemelytron. Shagreened (Fig. 2I). Legs. Coxae nearly glabrous; femora and tibiae covered fine, short, relatively dense, semi-recumbent setae; inner surface of fore femur with row of long, erect, simple setae along entire length. Abdomen. Covered with relatively dense and long semi-recumbent setae (Fig. 2B, C). STRUCTURE. Head. Porrect; vertex with moderately deep longitudinal depression along midline, posterior margin not carinate (Fig. 2E); clypeal base situated above ventral margin of eye (Fig.1F); mandibular plate without sulcus posteriorly (Fig. 2G); antennal insertion contiguous with sulcus between maxillary and mandibular plates (Fig. 2F); eyes contiguous with pronotal collar, relatively large, reniform in lateral view, reaching gula, almost wrapping head (Figs 2E–G); antennomere I rather long, weakly curved near base (Figs 2A, C, D); antennomere II thinner than antennomere I, somewhat arcuate, weakly broadened toward apex (Fig. 2A); labium thin, weakly reaching beyond hind coxae (Fig. 2B); segment I subdivided near medial portion (Figs 2B, G); segment II subdivided subapically. Thorax. Pronotum. Trapeziform, short (Figs 1, 2A); lateral margin elevated, strongly carinate, weakly arcuate (Figs 2G, H); calli upraised, separated by deep depression, long, almost reaching posterior margin of pronotum and broad but not reaching lateral margins (Figs 2A, G, H); humeral angles relatively thin and long (Figs 2A, H); posterior margin weakly sinuate (Fig. 2A). Mesoscutum and scutellum. Mesoscutum well exposed; scutellum moderately convex (Figs 2A, C). Thoracic pleura. Scent gland efferent system relatively broad, triangular; peritreme moderately upraised, ovoid (Fig. 2C). Hemelytron. Arcuate laterally; embolium wide; hemelytral veins convex; membrane with two cells (Fig. 2A). Legs. Not modified; relatively long (Fig. 2A); tarsi of each leg missing in examined specimen. Abdomen. Female genitalia. Genital chamber mostly membranous, voluminous, moderately expanded laterally beyond gonapophyses 8, semicircular (Figs 3A–F); sclerotized rings thin rimmed, relatively broad, almost entirely enveloping lateral portion of genital chamber (Figs 3A–C), posterior edge of sclerotized rings weakly folded (Figs 3C, F); lateral oviducts moderately thick, their bases moderately removed from each other (Fig. 3B); vulvar area with strongly developed sclerotizations (Figs 3C–F); genital chamber posterior wall with lateral margins of interramal sclerite thickened (Fig. 3G); ovipositor thin; apex of gonapophyses 8 and 9 obtuse, without any teeth (Figs 3I, J); gonapophyses 8 connected by delicate membrane along entire length, this membrane furnished with thin, elongated sclerotization originating near base of gonapophyses 8 and terminating near apex (ss) (Figs 3D, E, H).</p><p>Remarks. Gorczyciana gen. nov. is readily recognized by the unique set of the diagnostic characters that is not found in other Cylapinae . The new genus is assigned to the tribe Fulviini based on characters provided by Gorczyca (2000) as diagnostic for the tribe such as horizontal head, forecoxae and fore-femora enlarged, labium reaching the middle of abdomen. Other features allowing for a placement in Fulviini commonly found in the tribe are: labial segments I and II subdivided (Figs 2C, G), clypeal base situated well above the ventral margin of the eye (Figs 2C, F, G); antennal insertion contiguous with sulcus between maxillary and mandibular plates (Fig. 2G); eye enlarged, reniform, its ventral margin reaching gula (Figs 2C, F, G); mandibular plate without sulcus posteriorly; bursa copulatrix relatively thin, not reaching laterally beyond rami of the first valvulae (Figs 3A, B, D). (Wolski &amp; Henry 2012, 2015; Wolski et al. 2017; Namyatova &amp; Cassis 2019 a, 2021, 2022; Wolski 2021).</p><p>Gorczyciana is similar and possibly closely related to such fulviine genera as Cassisotropis Taszakowski et al. (Madagascar), Ceratofulvius Reuter (Australia), Euchilofulvius Poppius (Oriental and Australian Regions), Fulvius Stål (species belonging to the anthocoroides group–cosmopolitan), Peritropis Uhler (cosmopolitan), Peritropisca Carvalho &amp; Lorenzato (Australian Region), Rewafulvius Carvalho (Fiji) or Sulawesifulvius Gorczyca, Chérot &amp; Štys 2004 (Sulawesi) in sharing dorsum verrucose or with net-like sculpture comprised of tuberculate microsetae (Gorczyca &amp; Wolski 2007: Fig. 9; Wolski &amp; Henry 2012: figs 27–32; Pluot-Sigwalt &amp; Chérot 2013; Gorczyca et al. 2020: fig. 2A; Wolski &amp; Gorczyca 2014: figs 29–31; Wolski et al. 2017: fig. 7; Namyatova &amp; Cassis 2019; fig. 18J; Taszakowski et al. 2022b: figs 2B–E).Among those genera Gorczyciana is most similar to Peritropis in both sharing the oval body (Figs 1, 2A) and short pronotum with somewhat elevated and strongly carinate lateral margin and the collar weakly separated from the remainder of pronotum (absent in some Peritropis species) (Fig. 2H; Wolski &amp; Henry 2012: fig. 2). Additionally, Gorczyciana and many species of Peritropis (pers. obs.) possess a long, thin sclerotization along the membrane connecting 8 gonapophyses (Figs 3D, E, H) and the vulvar area is furnished with strongly developed sclerotizations (Figs 3C–F), which also may indicate a close affinity between both taxa. The new genus, however, can be easily distinguished from Peritropis in having the antennomere I about as long as head length (Fig. 2A), the strongly upraised pronotal calli (Figs 2C, G), the wide embolium, and the convex hemelytral veins (Fig. 3A). Similar structure of pronotum is also found in the genus Sulawesifulvius Gorczyca, Chérot &amp; Štys, 2004 (Gorczyca et al. 2004). The latter can, however, be easily distinguished from both genera by having the antennomere III the longest, the cuneus long, curved, nearly enveloping membrane, and the enlarged metafemur with subapical depressions laterally (Gorczyca et al. 2004). Gorczyciana somewhat resembles the Madagascan genus Cassisotropis in both having the apically serrate bristles on head and pronotum (Fig. 2 E; Taszakowski et al. 2022b: 2 B) at the same time having the weakly developed pronotal collar separated from the remainder of pronotum by shallow suture (Fig. 2E; Taszakowski et al. 2022b: fig. 2B). Also, both genera have upraised and acute calli although in Cassisotropis they are proportionally smaller than remainder of the pronotum (Taszakowski et al. 2022b: 2 B) whereas in Gorczyciana they calli occupy most of pronotum (Fig. 2A). Additionally, both genera can be readily separated by the position of the lateral margin of pronotum which is elevated in Gorczyciana (Figs 2A, H) and depressed in Cassisotropis (Taszakowski et al. 2022b: fig. 2B). Another feature discriminating those two genera is the structure of the posterior lobe of pronotum which is flattened in the new genus (Fig. 2H) and possessing weakly raised tubercles, each situated mediolaterally, bordering posterior margin in Cassisotropis (Taszakowski et al. 2022b: fig. 2B). In the latter genus the vulva is devoid of sclerotized structures (Taszakowski et al. 2022b: fig. 4C) whereas Gorczyciana has the vulvar area furnished with strongly developed sclerotizations (Figs 3C–F). The new genus is somewhat similar to the Australian genus Ceratofulvius in sharing similar mottled coloration (Namyatova &amp; Cassis 2019a: figs 5) and some structural features of the head, pronotum and female genitalia such as for example the upraised pronotal calli (Namyatova &amp; Cassis 2019a: figs 5, 16A, B, 18B, C). Both genera can, however, be easily distinguished the structure of the pronotal collar (well developed, separated from the remainder of the pronotum by the deep furrow in Ceratofulvius) (Namyatova &amp; Cassis 2019a: fig. 16A, 18B) and the metathoracic scent gland evaporative area which in the new genus is moderately developed and triangular (Fig 2C) while in Ceratofulvius it is strongly broadened and semicircular (Namyatova &amp; Cassis 2019a: 18 J).</p></div>	https://treatment.plazi.org/id/260C87D6FFCE781DFF63B812FC6A9C5E	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Wolski, Andrzej;Taszakowski, Artur	Wolski, Andrzej, Taszakowski, Artur (2023): Gorczyciana sulawesica-a remarkable new plant bug genus and species (Heteroptera: Miridae: Cylapinae) from Indonesia. Zootaxa 5297 (2): 260-270, DOI: 10.11646/zootaxa.5297.2.5, URL: http://dx.doi.org/10.11646/zootaxa.5297.2.5
260C87D6FFCC7818FF63BE8EFB7B9FB6.text	260C87D6FFCC7818FF63BE8EFB7B9FB6.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Gorczyciana sulawesica Wolski & Taszakowski 2023	<div><p>Gorczyciana sulawesica sp. nov.</p><p>Diagnosis. See the generic diagnosis.</p><p>Description. Female. Ground dorsal color pale creamy-yellow with numerous reddish and brownish patches and stripes of different size (Figs 2A, B). Head. Creamy-yellow with reddish and brownish patches and stripes (Figs 2A, B); vertex with three pairs of distinct, red, small patches: one pair situated on medial portion of vertex margin, one contiguous with inner margin of each eye and one pair bordering posterior margin of frons, longitudinal sulcus of vertex with reddish patches laterally forming two distinct circular patterns, medial longitudinal depression yellow, weakly darker than remainder of head (Fig. 2A); frons with two longitudinal dark red patches laterally bordering inner margin of eye, frons also with distinct creamy-yellow stripes bordering vertex, surface between vertex and frons also with similar creamy-yellow stripes, medially, frons also with red and dark yellow patches situated at obtuse angle to frons midline, sulcus on frons and surface bordering clypeus pale yellowish red (Fig. 2A); clypeus pale, creamy-yellow tinged with red dorsally, clypeal apex red; mandibular and maxillary plates with relatively large, brownish patches (Figs 2B); buccula red, with anterior small yellow tinge (Figs 2B); antennomere I creamy-yellow, with two red annulations; one basally and other close to base, apical three fourths with numerous reddish irregular fused patches (Figs 2A, B); antennomere II dark red with pale creamy-yellow stripe along inner surface (Figs 2A); labial segment I fuscous weakly tinged with yellow (Figs 2B); segment II dark yellow; segments III and IV fuscous. Thorax. Pronotum. Mostly creamy-yellow with numerous, more or less developed red spots and patches and pale fuscous tinge (Figs 2A, B); collar dark brown with broad color pattern medially composed of two creamy-yellow patches, each situated laterally, and one red situated medially (Figs 2A); lateral margin with small red spots along entire length (Figs 2A); calli densely sprinkled with small red spots (Figs 2A, B); posterior lobe broadly tinged with pale fuscous (Figs 2A); posterior margin with a few irregular, small pale yellow red spots along entire length (Figs 2A). Mesoscutum and scutellum. Ground coloration dark yellow with large black, reddish, and creamy-yellow areas (Figs 2A); medial part of mesoscutum and medio-basal part of scutellum with large black patch; mesoscutum sprinkled with brown and red sub-laterally and with two, relatively large patches, each situated laterally (Figs 2A); scutellum sprinkled with red and brown and with large creamy-yellow patch apically (Figs 2A). Thoracic pleura. Mostly yellow; dorsal portion of mesepimeron with red areas. Hemelytron. Ground coloration creamy-yellow with numerous red small spots and fuscous areas (Figs 2A); apical two thirds of clavus and three fourths of endocorium fuscous (Figs 2A); medial portion of exocorium and embolium pale fuscous (Figs 2A); claval and corial veins with small red spots along entire length (Figs 2A); embolium with irregular red spots along entire length (Figs 2A); cuneus pale fuscous, margins with red spots along entire length, numerous group of smaller red spots present on inner angle (Figs 2A); membrane pale fuscous, veins with fuscous spot along entire length (Figs 2A). Legs. Yellow brown, with red areas (Figs 2A, B); coxae yellow; fore coxa tinged with red basally (Figs 2B); fore femur yellow basally, remainder of fore femur fuscous tinged with yellow and red, apical portion yellow sprinkled with red (Figs 2A, B); middle femur yellow basally, remainder of middle femur red brown with numerous yellow patches, apex red (Figs 2A, B); hind femur yellow with basal half broadly tinged with red and brown, apex with two annulations: one composed of irregular brown patches subapically and other red apically (Figs 2A, B); tibiae yellow with numerous brownish and reddish irregular patches (Figs 2A, B).</p><p>Measurements. Female (n = 1). Body. Length: 4.7, width 2.1. Head. Length: 0.76, width: 0.84, interocular distance 0.4. Antenna. Length of antennomere I: 0.78, II: 1.80 (III and IV missing). Labium. Segments: I: 0.77. II: 0.82, III + IV: 1.34. Pronotum. Length: 0.85, length of lateral margin: 0.82, width of posterior margin: 1.56.</p><p>Male. Unknown.</p><p>Etymology. The specific epithet refers to the type locality.</p><p>Biology. Unknown, collected on light trap.</p><p>Distribution. Indonesia (Sulawesi).</p><p>Type material: Holotype ♀: Indonesia: SULAWESI, Ridge betw. Lake Metana and <a href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=121.46667&amp;materialsCitation.latitude=-2.55" title="Search Plazi for locations around (long 121.46667/lat -2.55)">Lake Mahalona. Kg. Salura</a>: 2 km SE Nightjar Camp. 600 m. 14.x.1993. Slightly distributed rain forest on ultrabasic soil 2º33’S, 121º28’E. At light. J.P. &amp; M.J. Duffels. (Zoological Institute, University of Copenhagen, Denmark - ZMUC).</p></div>	https://treatment.plazi.org/id/260C87D6FFCC7818FF63BE8EFB7B9FB6	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Wolski, Andrzej;Taszakowski, Artur	Wolski, Andrzej, Taszakowski, Artur (2023): Gorczyciana sulawesica-a remarkable new plant bug genus and species (Heteroptera: Miridae: Cylapinae) from Indonesia. Zootaxa 5297 (2): 260-270, DOI: 10.11646/zootaxa.5297.2.5, URL: http://dx.doi.org/10.11646/zootaxa.5297.2.5
260C87D6FFC87816FF63BCB1FA219C78.text	260C87D6FFC87816FF63BCB1FA219C78.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Fulviini Uhler 1886	<div><p>Key to tribes and genera of Fulviini of the Oriental Region</p><p>1. Antennal insertions removed from suture between maxillary and mandibular plates in dorsal direction (Namyatova et al. 2018: fig. 8C; Konstantinov 2012: fig. 4D); labium stout, segment IV not sharply pointed (as in Wolski 2021: figs 9j, k)......... 2</p><p>- Antennal insertions contiguous with suture between maxillary and mandibular plates (Fig. 3G; Wolski &amp; Henry 2012: fig. 73; Namyatova &amp; Cassis 2019b: fig. 2c); labium slender, segment IV sharply pointed (Namyatova &amp; Cassis 2019b: fig. 2g; Gorczyca et al. 2020: fig. 2C)........................................................................... 4</p><p>2. Head placed distinctly below posterior margin of pronotum (Namyatova et al. 2018: fig. C)............... Bothriomirini</p><p>- Head located at the same plane or higher than posterior margin of pronotum (Konstantinov 2012: 1 C; Yasunaga 2000: fig. 3). ................................................................................................... 3</p><p>3. Parempodia spatulate (Konstantinov 2012: fig. 4C).................................................... Vanniini</p><p>- Parempodia setiform (as in Wolski 2021: fig. 10n)..................................................... Cylapini</p><p>4. Antennae long, distinctly longer than body length (Namyatova &amp; Cassis 2019a: fig. 5); metathoracic scent gland evaporative area broad, somewhat expanded onto anterior margin of metepisternum, peritreme upraised, earlike (Namyatova &amp; Cassis 2019a: fig. 22E)............................................................................. Rhinomirini</p><p>- Antennae shorter than body length, if longer, then metathoracic scent gland evaporative area reduced, not reaching base of hind coxa and peritreme is weakly upraised oval (Wolski 2010: fig. 5B).............................................. 5</p><p>5. Frons strongly sloping; gula shorter than eye width in lateral view (Wolski &amp; Henry 2015: figs 18, 19).......... Psallopini</p><p>- Frons nearly horizontal or weakly sloping, if strongly sloping then gula is strongly protruding, in the form of disc (Carvalho 1986: fig. 2); gula longer than eye width in lateral view (Fig. 2B, C)..................................... 6 ( Fulviini)</p><p>6. Hemelytra distinctly punctate (Wolski 2010: fig. 1H-R; Tyts et al. 2022: 5 a, b; Wolski et al. 2016a: 1–8); if punctures are less distinct, antennae are longer than body length, third and fourth antennomeres together distinctly longer than second (Wolski 2010: figs 2A, D, F)................................................................................... 7</p><p>- Hemelytra impunctate (Fig. 2A): antennae always shorter than body length...................................... 10</p><p>7. Labial segment I without subdivision (Wolski 2010: fig. 5G, 7G); scent gland evaporative area reduced, not reaching base of hind coxa (Tyts et al. 2022: fig. 6g); left paramere distinctly rounded, with short, rounded process at apex (Wolski 2010: figs 6C, D, 12B, C); right paramere flattened, lateral margins nearly parallel-sided (Wolski 2010: figs 6E, 12D).................................................................... Rhinocylapus complex sensu Namyatova &amp; Cassis 20191</p><p>- Subdivision on labial segment I always present (Fig. 2G; Wolski &amp; Henry 2015: figs 20–24); scent gland evaporative reaching base of hind coxa.................................................................................... .. 8</p><p>8. Costal fracture present (Gorczyca &amp; Chérot 2001: fig. 1); length of the body less than 3.0 mm.......................................................................................... Teratofulvidius Gorczyca &amp; Chérot, 2001</p><p>- Costal fracture absent (Wolski et al. 2016a: 1–8); length of the body more than 3.0 mm.............................. 9</p><p>9. Pronotal collar absent (Wolski et al. 2016a: fig. 16)....................................... Fulvidius Poppius, 1909</p><p>- Pronotal collar present........................................................... Teratofulvius Poppius, 1914</p><p>10. Myrmecomorphic; gula strongly protruding, in the form of disc (Carvalho 1986: fig. 2)....... Gulacylapus Carvalho, 1986</p><p>- Gula normal in shape................................................................................. 11</p><p>11. Frons strongly projected forward, acute (Gorczyca 1996).................................. Rhinophrus China, 1944</p><p>- Frons without a spine................................................................................. 12</p><p>12. Gena convex (Wolski et al. 2016b: fig. 4A); claws not toothed subapically, inner surface of claws with distinct spine basally (Wolski et al. 2016b: 4 G, H)............................................... Hemiophthalmocoris Poppius, 1912</p><p>- Gena not convex; inner surface of claws without spine basally................................................. 13</p><p>13. Dorsum with small, regularly distributed callosities (Wolski &amp; Chérot 2008: fig. 1)..................................................................................................... Stysiofulvius Gorczyca &amp; Chérot, 2008</p><p>- Dorsum without small callosities, if callosities are present then pronotal collar is absent or weakly separated from remainder of pronotum and lateral margin of pronotum are strongly carinate ( similis group of the genus Peritropis Uhler) (Gorczyca 2006: fig. 8–11)......................................................................................... .. 14</p><p>14. Lateral margins of hemelytra more or less arcuate (Figs 1, 2A; Gorczyca 2006: figs 1–4; Gorczyca et al. 2004: fig. 1); pronotum elevated laterally (Figs 2A, H; Gorczyca 2006: figs 1–4); pronotal collar weakly separated from remainder of pronotum or absent (Fig. 2E, H).................................................................................. .. 15</p><p>- Lateral margins of hemelytra more or less straight and parallel (Yasunaga &amp; Miyamoto 2006: figs 5A, F); pronotum not elevated laterally; pronotal collar always present, separated from remainder of pronotum by deep depression............ 17</p><p>15. Antennomere III longest (Gorczyca et al. 2004: fig. 1); cuneus long, curved, nearly enveloping membrane (Gorczyca et al. 2004: fig. 1).................................................. Sulawesifulvius Gorczyca, Chérot &amp; Štys, 2004</p><p>- Antennomere III shorter, II longest; cuneus short, not enveloping membrane..................................... 16</p><p>16. Antennomere I as long as head length (Figs 1, 2A); pronotal calli strongly upraised (Figs 2 A-C, F, G); hemelytral veins convex along entire length (Fig. 2A)........................................................... Gorczyciana gen. nov.</p><p>- Antennomere I shorter than head; pronotal calli flat or weakly upraised; hemelytral veins not convex.. Peritropis Uhler, 1891</p><p>17. Pronotum carinate laterally; scent-gland evaporative area apparently absent or hardly visible (Wolski &amp; Gorczyca 2014: fig. 32); dorsum verrucose, covered with broad, scale-like setae, embolium narrowed basally, with a few small tubercles (Gorczyca 1998: fig. 1; Wolski &amp; Gorczyca 2014: fig. 29)...................................... Euchilofulvius Poppius, 1909</p><p>- Pronotum generally not carinate laterally; scent-gland evaporative area clearly present; body generally covered with simple setae, scale-like setae, if appear are linear (Wolski et al. 2018: figs 41–44); embolium not narrowed basally and without tubercles........................................................................................... 18</p><p>1 Keys to the genera of the Rhinocylapus group were provided by Wolski (2010) and Tyts et al. (2022).</p><p>18. Antennomeres III and IV as thick as antennomere II; head rugose (Schmitz 1978; Wolski 2008: fig. 1)................. 19</p><p>- Antennomeres III and IV thinner than antennomere II; head smooth............................................ 20</p><p>19. Head relatively short; pronotal calli not reaching lateral margins of pronotum............... .. Mimofulviella Wolski, 2008</p><p>- Head longer; pronotal calli reaching lateral margins of pronotum......................... .. Mimofulvius Schmitz, 1978</p><p>20. Eyes strongly removed from pronotal collar; profemur enlarged with thick spines on ventral surface (Stonedahl &amp; Kovac 1995: figs 6, 7).......................................................... Carvalhofulvius Stonedahl &amp; Kovac, 1995</p><p>- Eyes contiguous with pronotal collar, if slightly removed from pronotal, collar aperture of genital capsule oriented laterally; profemur without thick spines on ventral surface.......................................... 21 ( Fulvius Stål, 1862)</p><p>21. Dorsal surface covered with simple setae (Wolski et al. 2018: figs 27–30); second tarsomere divided medially, without subapical tooth (Wolski et al. 2018: figs 32, 33); genital opening of pygophore oriented laterally (Wolski et al. 2018: fig. 34); right paramere much smaller than left paramere (Wolski et al. 2018: figs 14, 15, 22, 23).................. bifenestratus group</p><p>- Dorsal surface covered with scale-like setae (Wolski et al. 2018: figs 41–44); second tarsomere not subdivided medially, toothed subapically (Wolski et al. 2018: figs 45–46); genital opening of pygophore directed posteriorly (Wolski et al. 2018: figs 47, 48); both parameres similar in size (Gorczyca et al. 2020: figs 4A, B)......................... anthocoroides group</p></div>	https://treatment.plazi.org/id/260C87D6FFC87816FF63BCB1FA219C78	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Wolski, Andrzej;Taszakowski, Artur	Wolski, Andrzej, Taszakowski, Artur (2023): Gorczyciana sulawesica-a remarkable new plant bug genus and species (Heteroptera: Miridae: Cylapinae) from Indonesia. Zootaxa 5297 (2): 260-270, DOI: 10.11646/zootaxa.5297.2.5, URL: http://dx.doi.org/10.11646/zootaxa.5297.2.5
