identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
462987920858DB1DFC1DFC4FFDC5375E.text	462987920858DB1DFC1DFC4FFDC5375E.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Adneella Carvalho 1960	<div><p>Adneella Carvalho, 1960</p><p>(Figs 1A, H, 2A, 3A, H, 5D, H, M, 6)</p><p>Tope species: Neella distincta Carvalho, 1945 . By original designation.</p><p>Adneella Carvalho, 1960: 47–49, 55 (original description; generic key; figs); Carvalho, 1985b: 290 (description of a new species); Carvalho and Schaffner, 1985: 4–7 (description of a new species); Carvalho and Froeschner, 1987: 124 (list); Carvalho, 1988: 79–80 (description of a new species); Carvalho, 1989a: 261–262 (description of a new species); Carvalho and Ferreira, 1995: 469, 476–477 (generic key); Schuh, 2002–13 (online catalogue); Coelho, 2008: 18, 24, 103, 111–112, 148 (generic key; distribution; figs); Ferreira et al., 2015: 252 (citation); Álvarez-Zapata et al., 2022: 101, 105–106, 109, 111, 114–115, 118, 124, 143 (generic and species key; figs; distribution).</p><p>Adparafurius Carvalho and Gomes, 1971: 461–462 (original description; figs); Carvalho, 1989b: 461–463, 482 (description of a new species; n. syn. of Adneella); Schuh, 2002–13 (online catalogue).</p><p>Included species: A. agripinoi Carvalho, 1988</p><p>A. amazonica Carvalho, 1989a</p><p>A. carioca Carvalho, 1985b</p><p>A. columbiensis (Carvalho and Gomes, 1971)</p><p>A. cuneata (Carvalho, 1954a), comb. nov.</p><p>A. decarloi (Carvalho, 1945), comb. nov.</p><p>A. distincta (Carvalho, 1945)</p><p>A. explanata (Carvalho, 1954a), comb. nov.</p><p>A. fumentaria (Distant, 1884), comb. nov.</p><p>A. nigronotata (Carvalho, 1954a), comb. nov.</p><p>A. osunai Carvalho, 1989b</p><p>A. panamensis Carvalho and Schaffner, 1985</p><p>A. putumaia Carvalho, 1989b</p><p>A. sp 1 sp. nov.</p><p>Diagnosis: Large, over 5mm (except female of A. decarloi comb. nov.); yellow with some orange to reddish or brown to black areas; eyes medium to large, sessile, inner margin inside or level with lateral collar margin; clypeus visible dorsally; vertex globose; antennal segment I widened towards apex; labium short, extending to middle of mesosternum; pronotal calli completely separated; posterior pronotal margin convex (straight in A. fumentaria comb. nov. and A. panamensis); veins roundly angled before the middle length of membrane, directed posteriorly and passing apex of cuneus; genital capsule with supragenital bridge strongly sclerotized and phallotheca slightly leaned to the lef relative to the phallobase.</p><p>Redescription: Male. TBL 5.89–8.48; PBL 4.98–7.47; BW 2.70– 3.85. Female. TBL 4.23–8.17; PBL 3.85–7.50; BW 1.94–3.48. Coloration: hemelytron yellow or yellow with black areas or black with yellow to red areas. Head: yellow, orange, or reddish, sometimes clypeus and apex of labium black; eyes black or silver; antennal segment I–II brown to black, III–IV brown, black, or pale yellow. Torax: pronotum yellow to reddish, or with posterior pronotal lobe dark brown; collar yellow, orange or black; mesoscutum yellow to reddish; scutellum brown to black or yellow, in some species yellow with dark areas; pleura yellow to reddish. Hemelytron: yellow, black, or yellow with brown to black areas; membrane and veins yellow or brown, or anterior half dark and posterior half yellow. Legs: coxae yellow or black; femora yellow, sometimes apex black; tibiae yellow or brown, or yellow with brown apex; tarsi yellow with apex brown in some species; claws brown. Abdomen: yellow or dark brown to black. Surface: shiny; posterior pronotal lobe evenly punctate; head dorsally with some recumbent setae, ventrally with longer and more abundant setae; antennal segment I with recumbent setae, II–IV with semierect setae; collar, pronotum, and hemelytra with abundant, short, semierect setae; veins of membrane with very short setae; pleura and abdomen with semierect setae; coxae, trochanters, femora, and tibiae with short, semierect setae, dorsal setae of femora usually as long as ventral setae. Structure: Head: more than 2× as wide as long; clypeus visible dorsally (except A. explanata comb. nov.), rounded in lateral view; frons rounded or flat in lateral view; vertex globose, wider than head length; eyes medium to large, sessile, more than half head height, upper margin not ataining dorsal margin of head, inner and posterior margins straight; inner margin inside or at level with lateral collar margin; labrum rounded in lateral view, long; gula visible; labium extending to mesosternum; antennal segment I long, widened towards apex; II, thinner and longer than I; III, thinner than II, narrowing towards apex; IV slender. Torax: anterior margin of collar straight or concave and posterior margin convex; pronotum bell-shaped; calli small to large, separated from each other by a median depression; posterior pronotal lobe flat, with shallow lateral depressions before humeral angles, posterior margin convex (straight in A. fumentaria comb. nov. and A. panamensis); mesoscutum exposed. Hemelytron: lateral margins parallel to convex; R + M extending to cuneal fracture; cuneus longer than wide, inner margin straight; veins roundly angled before the middle length of membrane, directed posteriorly, and passing apex of cuneus. Legs: profemora slightly widened at base; metafemora slightly curved. Male genitalia: genital capsule short, less than one-quarter of abdomen length, wider than long; genital aperture small and facing caudally; right wall as long as lef wall; dorsal wall less developed than ventral wall; supragenital bridge strongly sclerotized. Lef paramere similar to right paramere, strongly curved, hook-shaped; basal and apical processes narrower than body. Right paramere curved; basal and apical processes narrower than body. Aedeagus small; phallotheca membranous with some sclerotized areas or totally sclerotized, curved and slightly curving to the lef relative to the phallobase; seminal duct broad, membranous and slightly folded basally; apex of endosoma sclerotized.</p><p>Distribution: Argentina, Bolivia, Brazil, Colombia, Costa Rica, Ecuador, El Salvador, Panama, Peru, and Venezuela (Fig. 6).</p><p>Discussion: Te phylogenetic analysis recovered this genus as originally conceived as paraphyletic and as the sister-group of the clade formed by Pocnoderes quadrimaculatus + ( Parafurius discifer + Paraneella amazonica). It is supported by 12 synapomorphies. Five continuous characters: total length (0:078– 0792), and the following relations: labrum length/labial segment I length (4: 0.123 –0.124), antennal segment I, length/ antennal segment II (6: 0.229 –0.244), medial fracture length/ corium length (14:0.028), and genital capsule length/abdomen length (16:0.011); six discrete contradictory synapomorphic characters: labrum slightly globose (29:1), surface of collar smooth (43:0) and with recumbent setae (45:0), calli separated (48:0), inner margin of cuneus sinuate (71:1), medial angle of membrane cell acute (77:1), and supragenital bridge present (111:1); and a discrete synapomorphic character: phallotheca slightly inclined to the lef (147:0). Te GC frequencies indicate a low support due to high contradictory information (Fig. 7).</p><p>Carvalho (1960), in the original description of Adneella, stated that it is related to Neella, Neoneella, Paraneella, and Proneella . In our results, Adneella and Paraneella are located in a different clade from Neella, Proneella, and Neoneella, showing a more distant and complex relationship than assumed previously. In addition, Carvalho (1960) designated Neella distincta as type species, and suggested that four Neella species should also be transferred to this genus. In our analysis, Carvalho’s (1960) hypothesis was verified and Neella explanata, Neella fumentaria, Neella cuneata, and Neella nigronotata are transferred to Adneella, as well as Neella decarloi .</p><p>Egerocoris Mingheti et al., 2024</p><p>Tope species: Egerocoris ecuatorianus Mingheti et al., 2024 . By original designation.</p><p>Egerocoris Mingheti et al., 2024: 2–4 (original description; figs).</p><p>Included species: E. chaparensis Mingheti et al., 2024 E. dimorphus Mingheti et al., 2024</p><p>E. ecuatorianus Mingheti et al., 2024</p><p>Discussion: Tis genus was recently described to include three species from Bolivia and Ecuador. Egerocoris is recovered as the sister-group of the clade, including Neoneella and Puncticollus gen. nov., and is supported by six synapomorphies: five discrete contradictory synapomorphic characters: eyes covering laterally collar (22:1), dorsal wall of genital capsule with sclerotizations (97:1), posterior margin of ventral wall of the genital capsule sinuate (103:0), lef wall of genital capsule shorter than right wall (107:2), and lef paramere triangular (136:1), and one discrete synapomorphic character: lef paramere with distal extreme basally curved (141:1). For a detailed description and discussion of the genus see Mingheti et al. (2024).</p></div>	https://treatment.plazi.org/id/462987920858DB1DFC1DFC4FFDC5375E	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.		Plazi	Mingheti, Eugenia;Montemayor, Sara Itzel;Dellapé, Pablo Matías	Mingheti, Eugenia, Montemayor, Sara Itzel, Dellapé, Pablo Matías (2025): Phylogenetic revision of the Neella-Neoneella complex (Hemiptera: Heteroptera: Miridae: Bryocorinae), with description of five new genera. Zoological Journal of the Linnean Society 204 (2), DOI: 10.1093/zoolinnean/zlaf043, URL: https://doi.org/10.1093/zoolinnean/zlaf043
46298792085EDB1EFEDBF983FD8B3700.text	46298792085EDB1EFEDBF983FD8B3700.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Globicephalomiris Mingheti & Montemayor & Dellapé 2025	<div><p>Globicephalomiris gen. nov.</p><p>(Figs 1I, K, 2B, 4 A–D, 8)</p><p>Tope species: Neella pallescens Carvalho and Schaffner, 1985 . By present designation.</p><p>Included species: htp://zoobank.org/ urn:lsid:zoobank. org:pub: 465E9E66-F5ED-4820-9A02-D2E43F4ABFA0 G. carmelitana (Carvalho, 1945), comb. nov.</p><p>G. oaxacana (Carvalho and Schaffner, 1985), comb. nov.</p><p>G. pallescens (Carvalho and Schaffner, 1985), comb. nov.</p><p>G. veracruzana (Carvalho and Schaffner, 1985), comb. nov.</p><p>Diagnosis: Small, less than 4 mm; eyes covering collar in lateral view; clypeus not visible in dorsal view, basal half bulging; frons globose; vertex convex; labium extending to half of mesosternum; antennal segment I cylindrical; medial fracture adjacent to R + M; inner margin of cuneus straight; total overlap between inner margin of cell with hemelytra in repose; membrane unicolorous; right paramere rectangular, larger and more flatened than lef, without projections; phallobase tilted to right side and phallotheca curved to lef side.</p><p>Description: Male. TBL 3.71–3.99; PBL 3.15–3.81; BW 1.41– 1.87. Female. TBL 4.00; PBL 3.52; BW 1.55 (only a female of G. pallescens comb. nov. was measured). Coloration: Head: yellow to orange, apex of clypeus dark red to dark brown in some specimens; eyes black or silver, or black with silver areas; antennal segments brown, I–II with yellow areas. Torax: pronotum yellow or orange, with brown to black areas in some species; collar yellow or orange; mesoscutum and pleura yellow to orange; scutellum yellow to orange, in some specimens with brown areas. Hemelytron: yellow, with small brown or black areas on embolium, corium and clavus in some species, or orange with brown to black areas on embolium, corium, clavus and cuneus; membrane brown or greyish; veins brown or yellow. Legs: coxae yellow; femora and tibiae yellow, apex brown to black; tarsi brown or yellow; claws brown. Abdomen: yellow, orange or brown, or combined. Surface: Shiny; posterior pronotal lobe evenly punctate; head, pronotum, and hemelytra with short and recumbent setae; labium with semierect setae; antennal segments with semierect setae or segment I with recumbent setae and III–IV with erect setae; veins with very short, recumbent setae; pleura and abdomen with semierect setae, longer than dorsum; coxae, trochanters, femora and tarsi with semierect or erect setae; femora with dorsal setae as long as ventral setae; tibiae with abundant semierect setae. Structure: Head: more than 2× as wide as long; clypeus prominent, basal half bulging; frons globose in lateral view; vertex convex, wider than head length; eyes large, at maximum half of head height, sessile, covering collar in lateral view, upper margin ataining or not ataining dorsal margin of head, inner margin straight, at level with lateral margins of collar; gula well developed; labium extending to half of mesosternum; antennal segment I straight; II, straight, thinner and longer than I; III, tapering towards apex, thinner than II; IV, as thin as III. Torax: anterior margin of collar concave and posterior margin straight; calli slightly to strongly evident, connected or not in central area, attaining or not lateral margins of pronotum; posterior pronotal lobe with shallow lateral depressions before humeral angles; posterior margin convex or straight; mesoscutum exposed or not exposed; scutellum with or without basal depression. Hemelytron: embolium bent upwards or not; passing or not apex of abdomen; medial fracture shorter than half of corium, adjacent to R + M; claval commissure less than 2× as long as scutellum; cuneus longer than wide; inner margin straight; veins angled in middle of membrane, before or beyond apex of cuneus; inner and posterior margins of cell straight, most of species with total overlap between inner margin of cell with hemelytra in resting position. Legs: profemora widened basally; meso- and metafemora straight; metafemora slightly curved; protibiae slightly flatened distally; meso- and metatibiae straight. Male genitalia: genital capsule wider than long; genital opening broad or small, facing caudally; right wall as long as than lef; dorsal wall can be reduced; ventral wall more developed than dorsal; supragenital bridge present or absent. Lef paramere smaller than right, curved, hook-shaped; broad basally and narrow distally. Right paramere wider and longer than lef, slightly to strongly curved, flatened; apex broad and rounded. Aedeagus small and simple; phallobase lean to right side, membranous, with some sclerotized areas distally, curved to lef side; seminal duct membranous and not folded initially, sclerotized posterior to its distal curvature, extending at least to apex of phallotheca; endosoma membranous.</p><p>Distribution: Brazil, Colombia, Mexico, and Nicaragua (Fig. 8).</p><p>Etomologo: Te genus name is derived from the Latin word ‘ globus ’, meaning globe, and the Greek word ‘ kephalé ’, meaning head, due to its globose frons and vertex, in combination with the suffix ‘ miris ’ in reference to its assignment to the family Miridae . Te gender is feminine.</p><p>Discussion: Tis new genus includes four species transferred from Neella, N. carmelitana, N. oaxacana, N. pallescens, and N. veracruzana . In our analysis Globicephalomiris gen. nov. is recovered as monophyletic supported by nine synapomorphies. One continuous character:the relation posterior pronotal margin width/anterior pronotal margin width (11: 0.198 –0.206); five discrete contradictory synapomorphic characters: eyes covering collar in lateral view (22:1), clypeus not visible in dorsal view (27:0), frons globose (30:1), antennal segment I cylindrical (37:0), membrane unicolorous (158:0), and three discrete character: clypeus with a basal bulge (28:1), right paramere rectangular, without projections (125:1), phallobase curving to the right side (144:1). Globicephalomiris gen. nov. is hypothesized as the sister-group of the clade formed by Adneella + Paraneella + Parafurius discifer + Pocnoderes quadrimaculatus. Te GC frequencies indicate a high support due to low contradictory information (Fig. 7).</p><p>Globicephalomiris gen. nov. runs to couplet 46 in the key to the Neotropical eccritotarsine genera (Carvalho and Ferreira 1995) where the monotypic Tomascoris Carvalho, 1985a and Pachomerocerus Reuter, 1909 are identified. Tomascoris henroi Carvalho, 1985a has a pronotum and scutellum heavily punctate and with abundant pilosity on the antennae, legs, and body, and a genital capsule with two dorsal projections. Pachomerocerus species exhibit a convex, declivent anteriorly and subtriangular pronotum, with the posterior margin 2× longer than head width, the antennal segments I and II conspicuously wider than III and IV, and the genital capsule with dorsal projections. Globicephalomiris gen. nov. has a posterior pronotal lobe evenly punctate, with the posterior margin barely longer than the head width, the antennal segments I and II not evidently widened and the genital capsule without projections.</p><p>Four Neotropical genera were omited in Carvalho and Ferreira (1995)´s key ( Perissobasis Reuter, 1892, Eurocipitia Reuter, 1905, Bugabacoris Carvalho and China, 1959, and Pocnoderiella Henry, 1993) and five genera were described afer 1995 ( Cubanomiris Hernández and Stonedahl, 1996 and Agaveocoris, Laterospinocoris, Nigrotomocoris, and Schaffnerocoris, described by Henry and Menard, 2020). Te combination of characters given in the diagnosis distinguish Globicephalomiris gen. nov. from all the other eccritotarsines.</p></div>	https://treatment.plazi.org/id/46298792085EDB1EFEDBF983FD8B3700	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.		Plazi	Mingheti, Eugenia;Montemayor, Sara Itzel;Dellapé, Pablo Matías	Mingheti, Eugenia, Montemayor, Sara Itzel, Dellapé, Pablo Matías (2025): Phylogenetic revision of the Neella-Neoneella complex (Hemiptera: Heteroptera: Miridae: Bryocorinae), with description of five new genera. Zoological Journal of the Linnean Society 204 (2), DOI: 10.1093/zoolinnean/zlaf043, URL: https://doi.org/10.1093/zoolinnean/zlaf043
46298792085DDB01FED4F9D5FD0C371C.text	46298792085DDB01FED4F9D5FD0C371C.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Laterocavocoris Mingheti & Montemayor & Dellapé 2025	<div><p>Laterocavocoris gen. nov.</p><p>(Figs 2C, 3B, I, 4E–H, 5F, G, 6)</p><p>Tope species: Eccritotarsus lutescens Stål, 1860 . By present designation.</p><p>Included species: htp://zoobank.org/ urn:lsid:zoobank. org:pub: C0D3E979-1137-445B-BFEC-A90B175A82FD L. lutescens (Stål, 1860), comb. nov.</p><p>L. sp 1 sp. nov.</p><p>Diagnosis: Eyes large, stylate, upper margin overcoming dorsal margin of head; clypeus longer than half of head height, apex slightly depressed; antennal segment I straight and wider than II; labium extending to abdominal segment III; calli evident and small, not ataining lateral pronotal margins; embolium bent upwards in less than half of its length; medial fracture longer than one-third of corium length; inner margin of cuneus concave with apex truncate; supragenital bridge well developed; genital aperture small; dorsal wall of genital capsule with posterior margin sinuate; right projection of subgenital plate larger than lef, strongly curved and directed upwards, with central depression; and right paramere abruptly widened distally.</p><p>Description: Male. TBL 4.51–5.04; PBL 4.42–4.61; BW 2.18– 2.21. Female. TBL 4.94; PBL 4.61; BW 2.21. Coloration: Head: pale yellow; eyes brown to black; antennal segments I–II brown; III–IV, pale yellow. Torax: pronotum, mesoscutum, and pleura pale yellow to yellow; scutellum pale yellow with lateral margins brown. Hemelytron: pale yellow to yellow; membrane yellow; veins pale yellow to yellow. Legs: pale yellow to yellow. Abdomen: pale yellow to yellow. Surface: Shiny; posterior pronotal lobe evenly punctate; head, pronotum, and hemelytra with short and recumbent setae; labium with semierect setae; antennal segments I–II with short and recumbent setae; III–IV with semierect setae; veins with minute and recumbent setae; pleura and abdomen with semierect setae, longer and more dispersed setae than dorsum; coxae, trochanters, femora, and tarsi with short and recumbent setae. Structure: Head: more than 2× as wide as long. Clypeus not prominent, flat, longer than half of head height; apex slightly depressed; frons rounded; vertex flat, wider than length of head; eyes large, stylate, upper margin overcoming dorsal margin of head, more than half of head height, inner margin straight, at level with lateral margins of collar; maxillary plates large and broad; gula not visible or short; antennal segment I straight; II, straight, thinner, and more than 2× as long as I; III, tapering towards apex; IV, straight. Torax: collar evident, anterior margin concave and posterior margin straight; calli evident, small, separated, not ataining lateral margins of pronotum; posterior pronotal lobe with shallow depression separating humeral angles; posterior margin straight; mesoscutum exposed; scutellum with basal depression. Hemelytron lateral margins convex; embolium bent upwards in less than half of its length; medial fracture shorter than half of corium, anterior half adjacent to R + M vein, posterior half separated from R + M vein; R + M not ataining cuneal fracture; cuneus longer than width, inner margin concave with apex truncate; veins angled before or at central area of membrane, before apex of cuneus; cell with inner margin straight or convex, and posterior margin straight. Legs: profemora widened basally; meso- and metafemora straight; metafemora curved; apex of protibiae flatened internally; meso- and metatibiae straight. Male genitalia: Genital capsule less than or equal to one-third of abdomen length; wider than long; genital aperture small, facing caudally or dorsally; right wall shorter than or equal to lef; dorsal wall well developed or reduced, posterior margin sinuate with projections; ventral wall more developed than dorsal, posterior margin convex; subgenital plate with two processes, lef less developed and straight, and right larger and curved, directed dorsally, with a central depression and complex shape; supragenital bridge well developed. Lef paramere: basal process narrow; body curved, narrowed before apical process or medially. Right paramere wider than lef; basal process narrow; body abruptly widened. Aedeagus small and simple; phallotheca almost completely membranous, with some areas sclerotized dorsally; seminal duct widened initially, sclerotized posterior to its distal curvature; endosoma membranous.</p><p>Distribution: Brazil and Peru (Fig. 6).</p><p>Etomologo: Tis genus is named for the lateral and right projection of the subgenital plate, in combination with the Latin word ‘ cavo ’ from ‘ cavus ’ meaning hollow or concave, and the suffix ‘ coris ’ meaning bug. Te gender is feminine.</p><p>Discussion: Laterocavocoris gen. nov. includes one species transferred from Neella, N. lutescens, and a new as yet undescribed species. Laterocavocoris gen. nov. is recovered as monophyletic supported by 10 synapomorphies. Five continuous characters: the relations, clypeus length/head height (3:0.047), labial segment I length/vertex width (8:0.122), width of anterior margin of scutellum/scutellum length (12: 0.135 –0.137), cuneus length/anterior cuneal margin width (15:0.137) and aedeagus length/genital capsule length (18:0.077); three discrete contradictory synapomorphic characters: the sinuate posterior margin of dorsal wall of the genital capsule (96:2), genital capsule with a reduced opening (110:1) and supragenital bridge present (111:1); and two discrete characters: right process of the subgenital plate with a central concavity directed ventrally (116:1) and distal extreme of the right paramere abruptly and strongly expanded (129:1). Te GC frequencies indicate good support due to low contradictory information (Fig. 7).</p><p>Laterocavocoris gen. nov. runs to the couplet 8 in the key to the Neotropical eccritotarsine genera (Carvalho and Ferreira 1995), where Hesperolabops Kirkaldy, 1902 and Aztecarina Carvalho, 1974a are identified. Hesperolabops species have the head with long eye stalks and the hemelytra red or fuscous, and Aztecarina have strongly stylate eyes, the pronotum narrowed and constricted anteriorly with the posterior margin strongly arcuate at middle and the hemelytra punctate. In contrast, Laterocavocoris gen. nov. has slightly stylate eyes, the pronotum is not strongly narrowed or constricted anteriorly with its posterior margin straight, and the hemelytra are impunctate, yellow to pale yellow.</p><p>Four Neotropical genera were omited in the Carvalho and Ferreira (1995)´s key and five genera were described afer 1995 (see Globicephalomiris gen. nov. discussion for more details). Te combination of characters given in the diagnosis distinguish Laterocavocoris gen. nov. from all other eccritotarsines.</p></div>	https://treatment.plazi.org/id/46298792085DDB01FED4F9D5FD0C371C	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.		Plazi	Mingheti, Eugenia;Montemayor, Sara Itzel;Dellapé, Pablo Matías	Mingheti, Eugenia, Montemayor, Sara Itzel, Dellapé, Pablo Matías (2025): Phylogenetic revision of the Neella-Neoneella complex (Hemiptera: Heteroptera: Miridae: Bryocorinae), with description of five new genera. Zoological Journal of the Linnean Society 204 (2), DOI: 10.1093/zoolinnean/zlaf043, URL: https://doi.org/10.1093/zoolinnean/zlaf043
462987920842DB00FE90F9C1FD7136F6.text	462987920842DB00FE90F9C1FD7136F6.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Lelena Mingheti & Montemayor & Dellapé 2025	<div><p>Lelena gen. nov.</p><p>(Figs 2D, 9)</p><p>Tope species: Neella guiana Costa et al., 2008. By present designation.</p><p>Included species: htp://zoobank.org/ urn:lsid:zoobank. org:pub: 908E82A1-7838-45C1-810B-C1E18DD13264 L. cinnamomea (Carvalho and Gomes, 1971), comb. nov.</p><p>L. guiana (Costa et al., 2008), comb. nov.</p><p>L. unicolor (Hsiao, 1946), comb. nov.</p><p>Diagnosis: Yellow to orange; eyes sessile or slightly stylate; frons globose in lateral view; antennal segment I with recumbent and sparce erect setae, wider than II; calli not evident, separated; posterior pronotal margin straight; embolium not passing apex of abdomen; tibiae with only semierect setae; inner margin of cell convex and posterior margin straight; lef paramere curved and with apical process bifurcate with an expansion.</p><p>Description: Female. TBL 3.49–4.90; PBL 3.20–4.40; BW 1.44–2.08. Coloration: Head: yellow to orange; eyes silver, black or black with silver areas; antennal segment I yellow, orange, or brown; II, brown, dark brown, or yellow and brown; III, yellow basally, brownish distally; IV, brownish. Torax: pronotum, mesoscutum, and scutellum yellow to orange or orange with brown areas; pleura yellow to orange, in one species propleura bicoloured. Hemelytron: yellow to orange, or brown with basal area orange; membrane yellow to brown; veins yellow to brown. Legs: yellow to orange; tarsi pale yellow to orange; claws orange to brown. Abdomen: yellow to orange, in one species genital capsule brownish. Surface: Shiny; posterior pronotal lobe evenly punctate; head, pronotum, scutellum and hemelytra with abundant recumbent setae; labium with semierect setae; antennal segments I–II with short and recumbent setae, and sparce erect setae; III–IV, with semierect setae; veins with tiny and recumbent setae; pleura and abdomen with semierect setae, longer and more disperse setae than dorsum; legs with abundant semierect setae. Structure: Head: more than 2× as long as wide; clypeus not prominent, rounded in lateral view; frons globose in lateral view; vertex flat or convex; eyes sessile to slightly stylate, covering collar in lateral view, inner margin at level with or inside lateral margins of collar; gula not visible to short; labium extending to metacoxae or beyond; antennal segment II, straight, thinner and at least 2.5× as long as I. Torax: posterior margin of collar straight; calli not evident, separated and not ataining lateral margins of pronotum; posterior pronotal margin straight; mesoscutum exposed. Hemelytron lateral margins parallel to slightly convex; embolium flat, bent upwards, not passing apex of abdomen; claval commissure longer or shorter than scutellum and half of pronotum length combined; anterior half of medial fracture adjacent to R + M vein, posterior half separated from R + M vein; cuneus longer than wide, inner margin straight or slightly concave; veins angled in medial area of membrane and before apex of cuneus; inner margin of cell convex and posterior margin straight. Legs: profemora widened basally. Male genitalia: Lef paramere falciform; curved; apical process bifurcate with an expansion. Right paramere small, tapering towards apex.</p><p>Distribution: Argentina, Brazil, Ecuador, French Guiana, and Peru (Fig. 9).</p><p>Etomologo: Te generic name is an anagram of Neella, a genus in which the included species were originally described. Te gender is feminine.</p><p>Discussion: Lelena gen. nov. includes three species transferred from Neella ( N. cinnamomea, N. guiana, and N. unicolor) that share sessile or slightly stylate eyes, globose frons, first antennal segment with recumbent and sparce erect setae, calli not evident and separated, posterior margin of pronotum straight, and lef paramere curved and with a bifurcate apical process. In our analysis, this genus is supported by three synapomorphies: the continuous character relation: pronotum posterior margin width/ anterior margin width (11:0.179), and two discrete contradictory synapomorphies: embolium not extending posteriorly to the abdomen (65:1), and tibiae with one type of setae (89:0). Te GC frequencies indicate a low support due to high contradictory information (Fig. 7).</p><p>Lelena gen. nov. runs to the couplet 23 in the key to the Neotropical eccritotarsine genera (Carvalho and Ferreira 1995), where the genera Pachopoda Carvalho and China, 1951 and Stictolophus Bergroth, 1922 are identified. Pachopoda has a smooth pronotum with large calli and thick tibiae, incrassated toward apex, and Stictolophus is characterized by a large collar, sinuate anteriorly, and large calli separated by a deep median depression over posterior two-thirds, and thick profemora. In contrast, Lelena gen. nov. has a narrow collar, indistinct calli, and legs with only the profemora thickened basally.</p><p>Additional nine Neotropical genera are absent in Carvalho and Ferreira (1995)´s key (see discussion under Globicephalomiris gen. nov.). Te combination of characters given in the diagnosis distinguishes Lelena gen. nov. from all other eccritotarsines.</p></div>	https://treatment.plazi.org/id/462987920842DB00FE90F9C1FD7136F6	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.		Plazi	Mingheti, Eugenia;Montemayor, Sara Itzel;Dellapé, Pablo Matías	Mingheti, Eugenia, Montemayor, Sara Itzel, Dellapé, Pablo Matías (2025): Phylogenetic revision of the Neella-Neoneella complex (Hemiptera: Heteroptera: Miridae: Bryocorinae), with description of five new genera. Zoological Journal of the Linnean Society 204 (2), DOI: 10.1093/zoolinnean/zlaf043, URL: https://doi.org/10.1093/zoolinnean/zlaf043
462987920843DB03FBFCFB10FA3B352C.text	462987920843DB03FBFCFB10FA3B352C.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Naelle Mingheti & Montemayor & Dellapé 2025	<div><p>Naelle gen. nov.</p><p>(Figs 2E, 3C, J, 5E, J, 9)</p><p>Tope species: Neella ecuatoriana Carvalho and Wallerstein, 1978 . By present designation.</p><p>Included species: htp://zoobank.org/ urn:lsid:zoobank. org:pub: 25A5159E-A03D-4A02-8FBC-452632C9B 109 N. ecuatoriana (Carvalho and Wallerstein, 1978), comb. nov. N. itacoaiensis (Carvalho, 1954a), comb. nov.</p><p>N. sp 1 sp. nov.</p><p>Diagnosis: Orange to red; eyes large, stylate; vertex flat, slightly longer than width of head; clypeus longer than half of head height; embolium flat; medial fracture shorter than half of corium; inner margin of cuneus concave with apex truncate; inner and posterior margins of cell straight; profemora widened basally; genital capsule wider than tall, dorsal wall with a large projection in lef margin; lef paramere curved to strongly curved, with a distal concavity; right paramere widened medially; and seminal duct initially folded and extending to half of phallotheca length.</p><p>Description: Male. TBL 4.14–4.89; PBL 3.85–4.61; BW 1.80– 2.49. Female. TBL 4.18–5.22; PBL 3.67–4.75; BW 1.82–2.46.</p><p>Coloration: Head: pale yellow to orange; eyes black, silver, golden or black with silver areas; antennal segment I orange or brown; II, brown or orange basally and brown distally; III, pale yellow or pale yellow basally and reddish or brownish distally; IV, pale yellow or reddish basally and brown distally. Torax: pronotum orange or collar and calli paler and posterior lobe darker; mesoscutum and scutellum pale yellow to reddish; pleura pale yellow to orange. Hemelytron: yellow to reddish, in some specimens cuneus orange and reddish; membrane translucent; veins yellow to reddish. Legs: coxae pale yellow to orange; femora yellow or orange, in some specimens bicoloured; tibiae orange, apex yellow or brown; tarsi pale yellow; claws orange to brown. Abdomen: pale yellow to reddish, in some specimens with more than one colour. Surface: Shiny, posterior pronotal lobe evenly punctate; head, pronotum, and hemelytra with recumbent setae; labium with semierect setae; antennal segment I with abundant recumbent setae, II with recumbent and scattered semierect setae, III and IV with recumbent and semierect setae; veins with minute and recumbent setae; pleura and abdomen with longer semierect setae than dorsum; coxae, trochanters, femora, and tarsi with short, semierect setae; femora with dorsal setae as long as ventral setae; tibiae with abundant recumbent setae. Structure: Head: more than 2× as wide as long; clypeus not prominent, rounded in lateral view; frons rounded in lateral view; vertex flat, slightly longer than width of head; eyes large, stylate, more than half head height, upper margin attaining or overcoming dorsal margin of head, inner margin at level with lateral margins of collar; maxillary plates rectangular, medium to large; gula not visible to short; labium at least extending to mesocoxae; antennal segment I straight or slightly tapering towards apex; II, slightly widened towards apex, at least 2× as long as I; III, tapering towards apex, thinner than II; IV, straight. Torax: anterior margin of collar concave medially and posterior margin straight or convex; wider than antennal segment I; calli not evident to evident, separated, not ataining or ataining lateral margins of pronotum; posterior pronotal lobe with shallow depression separating humeral angles; posterior margin straight; mesoscutum exposed or not; scutellum in some species with a basal depression. Hemelytron with lateral margins slightly convex from apex of scutellum; embolium flat, in one species not bent upwards; medial fracture shorter than half of corium, anterior half adjacent to R + M vein, posterior half separated from R + M vein; R + M ataining or not cuneal fracture; cuneus longer than wide, inner margin concave; cell angled before apex of cuneus, inner and posterior margins straight. Legs: profemora widened basally, meso- and metafemora straight, metafemora slightly curved; protibiae with apex flatened, meso- and metatibiae straight. Male genitalia: Genital capsule wider than long; right wall shorter or longer than lef; dorsal wall well developed or reduced medially, posterior margin concave, with a large projection in lef margin; posterior margin of ventral wall sinuate or straight; subgenital plate in two species with two processes, lef one smaller and straight, and right longer and curved, with central depression. Lef paramere smaller than right, curved to strongly curved; with a distal concavity. Right paremere body flat and widened medially. Aedeagus small and simple; phallotheca membranous, some areas sclerotized; seminal duct sclerotized, folded initially, extending to half of phallotheca length; endosoma membranous.</p><p>Distribution: Brazil, Ecuador, Peru (Fig. 9).</p><p>Etomologo: Te generic name is an anagram of Neella, a genus in which two of the species included in this new genus were originally described. Te gender is feminine.</p><p>Discussion: Naelle gen. nov. is recovered as the sister-group of Proneella and includes two species transferred from Neella, Neella itacoaiensis and Neella ecuatoriana, and a new as yet undescribed species. In our analysis this genus is recovered as monophyletic supported by four synapomorphies. Tree continuous characters: the relations, eyes height/head height (1: 0.055 –0.058), vertex width/eye width (5: 0.194 –0.204), and labial segment II/ total labial length (9:0.3); and one discrete synapomorphic character: lef paramere with a concavity at distal extreme (139:1). Te GC frequencies indicate a low support due to high contradictory information (Fig. 7).</p><p>Naelle gen. nov. runs to the couplet 8 in the key to the Neotropical eccritotarsine genera (Carvalho and Ferreira 1995) in which Hesperolabops and Aztecarina are identified. Hesperolabops includes species with the head with long eye stalks and hemelytra red or fuscous, and Aztecarina species have strongly stylate eyes, the pronotum narrowed and constricted anteriorly with the posterior margin strongly arcuate at middle, and the hemelytra punctate. Naelle gen. nov. has slightly stylate eyes, pronotum not strongly narrowed or constricted anteriorly and with its posterior margin straight, and yellow to reddish impunctate hemelytra.</p><p>Nine Neotropical genera are absent in the Carvalho and Ferreira (1995) 's key (see discussion under Globicephalomiris gen. nov.). Te combination of characters given in the diagnosis distinguishes Naelle gen. nov. from all other eccritotarsines.</p></div>	https://treatment.plazi.org/id/462987920843DB03FBFCFB10FA3B352C	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.		Plazi	Mingheti, Eugenia;Montemayor, Sara Itzel;Dellapé, Pablo Matías	Mingheti, Eugenia, Montemayor, Sara Itzel, Dellapé, Pablo Matías (2025): Phylogenetic revision of the Neella-Neoneella complex (Hemiptera: Heteroptera: Miridae: Bryocorinae), with description of five new genera. Zoological Journal of the Linnean Society 204 (2), DOI: 10.1093/zoolinnean/zlaf043, URL: https://doi.org/10.1093/zoolinnean/zlaf043
462987920840DB05FBF4FB21FEC5327E.text	462987920840DB05FBF4FB21FEC5327E.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Neella Reuter 1908	<div><p>Neella Reuter, 1908</p><p>(Figs 1C, 2F, 3D, E, K, 5C, K, O, 8)</p><p>Tope species: Eccritotarsus eucosmus Stål, 1862 . By original designation.</p><p>Neella Reuter, 1908: 152–154 (original description); Reuter, 1910: 153 (catalogue); Bergroth, 1922: 17 (species transfer); Costa Lima, 1942: 103–104 (citation); Carvalho, 1945: 161– 172 (description of new species; redescription of known species; key); Hsiao, 1946: 385–387 (description of a new species; species transfer; key); Carvalho, 1948: 100, 103–104 (description of a new species); Carvalho, 1952: 56; Carvalho, 1954a: 1–19 (description of new species; redescription of known species; key); Carvalho, 1955: 32 (key); Carvalho, 1960: 47, 49 (key); Carvalho and Gomes, 1971: 466–468 (description of new species); Carvalho, 1974b: 324–325 (description of a new species); Carvalho and Schaffner, 1985: 7–14 (description of new species); Carvalho and Ferreira, 1995: 477 (key); Carpintero, 1998: 145 (citation); Kerzhner and Konstantinov, 1999: 124; Ferreira et al., 2001: 162 (distribution); Schuh, 2002–13 (online catalogue); Ferreira et al., 2006: 4, 10 (distribution); Coelho, 2008: 18, 25,104, 116, 149 (key; distribution); Ferreira and Henry, 2011: 2, 13, 19–20, 34 (key; distribution); Namyatova et al., 2016: 14 (citation); Etl et al., 2016: 300, 302–303 (host plants); Barbosa et al., 2019: 158 [ Neela misspelling] (host plant); Álvarez-Zapata et al., 2022: 101, 105, 107, 109–110, 114, 116, 129–130, 136, 144 (generic and species key; figs; distribution); Ferreira et al., 2024: 207, 214, 215, 222, 242 (diagnosis; generic key; figs).</p><p>Included species: N. bicolor Hsiao, 1946 N. carvalhoi Hsiao, 1946</p><p>N. eucosma (Stål, 1862)</p><p>N. fasciata Hsiao, 1946</p><p>N. floridula (Distant, 1883) N. mantiqueirae Carvalho, 1954a N. peruana Carvalho, 1974b N. similaris Carvalho and Gomes, 1971</p><p>Diagnosis: Orange to reddish, with brown to black areas in pronotum and hemelytra; eyes large, more than half of head height, posterior margin concave; vertex as maximum 2.5× as wide as one eye; posterior margin of head with a group of recumbent setae behind eyes; labrum flat in lateral view; labium at least extending to metacoxae; antennal segment II swollen subapically; anterior margin of collar concave; posterior pronotal margin straight, pronotal width across calli half as wide as posterior margin width; inner margin of cuneus concave; cell angled before apex of cuneus; tibiae with only one type of setae; lef paramere with two or three curvatures, tapering towards apex; right paramere different from lef, C-shaped, tapering towards apex.</p><p>Redescription: Male. TBL 4.00–5.89; PBL 3.38–5.32; BW 1.51–2.59. Female. TBL 3.47–5.70; PBL 3.19–5.22; BW 1.44–2.66. Coloration: Orange to reddish, with brown to black areas in pronotum and hemelytra. Head: pale yellow to reddish, sometimes with brown to black areas; eyes black, golden or silver, or black with golden or silver areas; antennal segments I–II yellow, orange, reddish or brown reddish; III, pale yellow to reddish or brown; IV, pale yellow to reddish, sometimes distal half brown. Torax: collar pale yellow to dark red or brown; calli pale yellow to reddish; posterior pronotal lobe pale yellow to dark red or brown, in some species with dark transverse fascia or semicircular area; mesoscutum and scutellum yellow to black; pleura pale yellow to reddish, in some species propleura bicoloured. Hemelytron: pale yellow to reddish, brown or black, unicolorous, or with longitudinal brown fascia extending to membrane; membrane translucent to black; veins yellow to black. Legs: pale yellow to dark brown; usually femora and tibiae bicoloured; tarsi and claws pale yellow to black. Abdomen: pale yellow to dark red. Surface: Shiny; posterior pronotal lobe evenly punctate; head, collar, pronotum, and hemelytra with short, recumbent or semierect setae; labium with semierect setae; antennal segments I–II with short and recumbent or semierect setae, sometimes with some erect setae; III–IV, with abundant recumbent to semierect setae; veins with very short and recumbent setae; pleura and abdomen with semierect setae, longer than dorsum; coxae, trochanters, femora, and tarsi with short and semierect setae; femora with dorsal setae as long as ventral setae; tibiae with thicker setae. Structure: Head: at least 2× as wide as long; clypeus not visible from above, flat or rounded in lateral view; frons rounded to globose in lateral view; vertex flat, as maximum 2.5× as wide as one eye; eyes large, stylate, more than half of head height, upper margin of eyes overcoming dorsal margin of head; posterior margin concave; gula not visible to short; labrum flat in lateral view; labium at least extending to metacoxae; antennal segment I straight; II more than 2× as long as I, swollen subapically; III, tapering towards apex; IV, straight and thinner than III; posterior margin of head with a group of recumbent setae behind eyes. Torax: anterior margin of collar concave and posterior margin straight or convex, thinner than antennal segment I; calli separated in central area, ataining or not lateral margins of pronotum; pronotal width across calli half as wide as posterior margin width, posterior margin straight; mesoscutum usually exposed; scutellum with basal depression. Hemelytron: lateral margins slightly convex to convex; embolium thin, bent upwards; claval commissure longer than scutellum and half of pronotum length combined; anterior half of medial fracture adjacent to R + M vein, posterior half separated from R + M vein; cuneus longer than wide, inner margin concave; cell angled before or in middle of membrane, before apex of cuneus, inner margin straight or convex and posterior margin straight or concave; veins angled before apex of cuneus. Legs: profemora widened basally; meso- and metafemora straight; metafemora slightly curved; protibia slightly flatened distally. Male genitalia: Genital capsule wider than long; genital opening broad, facing dorsally; right wall equal to or shorter than lef; dorsal wall well developed or reduced, in some species with projections, posterior margin concave; ventral wall more developed than dorsal, posterior margin convex, with one or two projections; subgenital plate with or without projections, ventral to parameres insertion. Lef paramere smaller than right, curved to sinuate; body with two or three curvatures, tapering towards apex; apical process rounded or pointed, in some species bifurcate. Right paramere different from lef, C-shaped; basal process narrow; apical process simple or bifurcate. Aedeagus small and simple; phallotheca membranous with some sclerotized areas; seminal duct folded initially, membranous, sclerotized posterior to its distal curvature or completely sclerotized, at least extending to half of phallotheca; endosoma membranous, in some species apex sclerotized.</p><p>Distribution: Argentina, Brazil, Colombia, Costa Rica, Ecuador, El Salvador, French Guiana, Guatemala, Honduras, Mexico, Panama, Paraguay, and Peru (Fig. 8).</p><p>Discussion: In our analysis Neella is highly polyphyletic, indicating several species require transfer to other known or to new genera. Te phylogeny recovers seven species in the Neella clade (plus N. similaris) and as the sister-group of the clade Egerocoris, Laterocavocoris gen. nov., Lelena gen. nov., Neoneella, and Puncticollus gen. nov. Te genus is supported by five synapomorphies, one continuous character: relation of posterior pronotal margin width/anterior pronotal margin width (11: 0.193 –0.198), three discrete contradictory synapomorphic characters: the cylindrical antennal segment II (38:0), tibiae with one type of setae (89:0) and the right paramere C-shaped in dorsal view (122:1), and a discrete synapomorphic character: lef paramere with a basal and distal curvatures in straight angle (137:1). Te GC frequencies indicate a low support due to high contradictory information (Fig. 7).</p><p>Troughout the years different authors have related Neella with other genera of Eccritotarsini. Reuter (1908) differentiated it from Sosinas Distant by the vertical position of the head, the flat vertex, the flatened clypeus in lateral view, the more rounded inner margin of the eyes, the long labium, the large and transverse calli, and the scutellum with a triangular depression at the anterior margin. Also, when Costa Lima (1942) described Neoneella he recognized its affinity with Neella, but distinguished them by the absence of sexual dimorphism in the development of the cuneus in Neella . Hsiao (1946) considered Neella closely related to Tenthecoris Scot, but pointed out that in Neella the body is more elongated, the lateral margins of the hemelytra are less convex, the vertex is flat, and the labium long, with segments III–IV short and thin. Finally, Carvalho (1960) highlighted that Neella is related to Adneella, Neoneella, Paraneella, and Proneella, transferring one species from Neella to Adneella and suggesting that four other species should also be transferred. In our hypothesis, Sosinas and Tenthecoris are located basally together with Paraneella, Adneella, Pocnoderes, Parafurius, and Globicephalomiris gen. nov., whereas Neella is related to Proneella and other genera (see ‘Phylogenetic results’ for a more detailed analysis of characters).</p></div>	https://treatment.plazi.org/id/462987920840DB05FBF4FB21FEC5327E	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.		Plazi	Mingheti, Eugenia;Montemayor, Sara Itzel;Dellapé, Pablo Matías	Mingheti, Eugenia, Montemayor, Sara Itzel, Dellapé, Pablo Matías (2025): Phylogenetic revision of the Neella-Neoneella complex (Hemiptera: Heteroptera: Miridae: Bryocorinae), with description of five new genera. Zoological Journal of the Linnean Society 204 (2), DOI: 10.1093/zoolinnean/zlaf043, URL: https://doi.org/10.1093/zoolinnean/zlaf043
462987920846DB04FED7FCE0FE6937BE.text	462987920846DB04FED7FCE0FE6937BE.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Neoneella da Costa Lima 1942	<div><p>Neoneella Costa Lima, 1942</p><p>(Figs 1E, F, 2G, 3F, G, L, 5A, B, I, P, 6)</p><p>Tope species: Neoneella zikani Costa Lima, 1942. By original designation.</p><p>Neoneella Costa Lima, 1942: 102–107 (original description); Hsiao, 1946: 385; Carvalho, 1946a: 1–8 (description of new species; key); Carvalho, 1946b: 1–2, 7, 9 (description of a new species); Carvalho, 1952: 57 (catalogue); Carvalho, 1955: 30 (key); Carvalho, 1957: 115–116 (catalogue); Carvalho, 1960: 47–50, 53, 55, 58–59 (description of a new species; key); Schuh, 1976: 9 (citation); Carvalho, 1985a: 571, 579-580 (description of a new species); Carvalho, 1985c: 169, 173–174 (description of a new species); Carvalho and Ferreira, 1995: 472, 481 (key); Carpintero, 1998: 145 (citation); Ferreira et al., 2001: 162 (distribution); Schuh, 2002–13 (online catalogue); Ferreira et al., 2006: 4, 10 (distribution); Coelho, 2008: 14, 18, 25, 103, 117– 118, 150 (key; distribution); Ferreira and Henry, 2011: 2, 12, 20, 36 (key; distribution); Ferreira et al., 2024: 213 (generic key).</p><p>Included species: N. argentina Carvalho, 1960</p><p>N. bosqi Carvalho, 1946b</p><p>N. milzae Carvalho, 1946a</p><p>N. minuscula Carvalho, 1985c</p><p>N. paranaensis Carvalho, 1946a</p><p>N. zikani Costa Lima, 1942</p><p>Diagnosis: Orange or reddish; some species with brown to black areas; eyes stylate, directed posteriorly, eye stalk narrowed; posterior margin of head without recumbent setae behind eyes; vertex concave; antennae longer in males; hemelytra with semierect setae (except N. milzae with erect setae); claval commissure more than 2× as long as scutellum length; sexual dimorphism in length and shape of inner margin of cuneus, males with cuneus more developed and its apex ataining posterior margin of membrane, which is reduced, and vein of cell straight, not curved as in females; right projection of subgenital plate asymmetrically bifurcate, ventral to the insertion of parameres and visible from outside of the genital capsule; right paramere with a triangular projection or big tooth on dorsal surface; lef paramere C-shaped with its apex bifurcate in upper view; and phallotheca with bulbous base.</p><p>Redescription: Male. TBL 5.23–7.55; BW 2.30–3.95. Female. TBL 5.32–6.66; PBL 5.13–6.37; BW 1.97–2.98. Coloration: Head: orange yellowish to reddish; eyes black, in some specimens with silver areas; antennal segments I–II, brown to black; III, pale yellow or dark brown; IV, blackish. Torax: pronotum unicolorous or bicoloured; collar mesoscutum, scutellum, and pleura orange or reddish. Hemelytron: reddish to brown, in some species yellow or reddish with brown areas in embolium, corium, clavus, and/or cuneus; membrane yellow, brown, or black; veins pale yellow to reddish or brown. Legs: coxae yellow, orange to reddish; femora yellow, orange or brown reddish; tibiae yellow, orange to dark brown; tarsi pale yellow and apex brown; claws brown. Abdomen: yellow, orange to reddish. Surface: Shiny; posterior pronotal lobe evenly punctate; head, collar, pronotum, scutellum, and hemelytra with short, recumbent, or semierect setae; labium with semierect setae; antennal segments with semierect setae, segment I with also some erect setae, in some species scattered erect setae on all segments; veins with very short and recumbent setae; pleura and abdomen with semierect setae, longer than dorsum; coxae, trochanters, and tarsi with short and semierect setae; femora with dorsal setae shorter than ventral setae; tibiae with abundant semierect or erect setae. Structure: Head: at least 2× as wide as long; clypeus not visible from above, rounded in lateral view; frons rounded in lateral view; vertex concave, wider than length of head; eyes large, more than half of head height, stylate, directed posteriorly, upper margin overcoming dorsal margin of head, inner margin straight and outside lateral margins of collar; eye stalk narrowed; posterior margin of head without recumbent setae behind eyes; labrum long; gula very short; antennal segment I wide basally, tapering towards apex; II, straight, thinner than and more than 2× as long as I; III, tapering towards apex, thinner than II; IV, straight and thin. Torax: anterior margin of collar concave and posterior margin straight; calli evident, not connected in central area, ataining or not lateral margins of pronotum; posterior pronotal lobe with shallow lateral depressions before humeral angles, posterior margin straight or sinuate; mesoscutum exposed; scutellum with basal depression. Hemelytron: lateral margins parallel to convex; embolium flat, bent upwards; claval commissure more than 2× as long as scutellum length; anterior half of medial fracture adjacent to R + M vein, posterior half separated from R + M vein; males with apex of cuneus ataining posterior margin of membrane and contacting each other with hemelytra in repose, inner margin concave, membrane reduced, and veins straight, not angled in middle of membrane, and ataining apex of cuneus; females with apex of cuneus not ataining posterior margin of membrane and not contacting each other with hemelytra in repose, membrane well developed, veins angled before middle area of membrane and before apex of cuneus, inner margin convex and posterior margin straight. Legs: profemora widened basally; meso- and metafemora straight; metafemora slightly curved; protibia slightly flatened distally; meso- and metatibiae straight. Male genitalia: Genital capsule shorter than half of abdomen length; genital opening broad, facing dorsally; right wall shorter than lef; dorsal wall well developed or reduced, with projections; ventral wall more developed than dorsal, posterior margin convex; subgenital plate with right projection asymmetrically bifurcate, ventral to paramere insertion, visible from outside of genital capsule. Lef paramere very curved, C-shaped, flat, smaller or larger than right; apical process bifurcate. Right paramere with basal, triangular projection or a big tooth directed dorsally; apical process with sclerotized teeth. Aedeagus small to large; phallotheca sclerotized or with some membranous areas, bulbous basally; seminal duct folded and widened initially, membranous, sclerotized posterior to its distal curvature, at least extending to half of phallotheca; endosoma membranous, sometimes sclerotized basally.</p><p>Distribution: Argentina, Brazil, Paraguay, and Uruguay (Fig. 6).</p><p>Discussion: Neoneella is recovered as sister-group of Puncticollus gen. nov. (Fig. 7). Neoneella is strongly supported by 20 synapomorphies. Four are continuous characters: total length (0: 0.672 –0.690), and the relations: antennal fossa length/ eye height (7:0.030), claval commissure length/scutellum length (13: 0.234 –0.242), and aedeagus length/genital capsule length (18: 0.119 –0.133); and five are discrete contradictory synapomorphic characters: eyes anteriorly directed (24:1), without a group of recumbent setae behind posterior margin of eye (32:0), semierect setae on hemelytra (62:1), and cuneus sexually dimorphic (68:1, 70:1); and 11 are discrete synapomorphic characters: vertex concave (31:0), length of antenna, membrane development, and cell length sexually dimorphic (34:1, 72:1, 74:1), medial angle of cell present only in females (76:1), lef wall of genital capsule more developed than right (107:1), processes of subgenital plate of genital capsule only in the right side (113:0) and asymmetrically bifurcate (117:1), right paramere with a triangular projection or large tooth on dorsal surface (121:1), lef paramere C-shaped with apex bifurcate in upper view (134:1), and phallotheca with bulbous base in ventral view (148:1). Te GC frequencies indicate a high support due to low contradictory information (Fig. 7).</p><p>Costa Lima (1942) recognized that Neoneella has similarities with Taumastomiris Kirkaldy in the development of the cuneus and in the length of the labium (long in both genera), and suggested that they could be synonymized. However, the eyes in Taumastomiris are less stylate and, at least in females, the posterior margin of the cuneus is narrow and reaches the posterior margin of the hemelytra, with the membrane veins straight ataining the apex of cuneus.</p><p>Proneella also has a sexually dimorphic cuneus, with males having a longer cuneus than females, but it does not extend to the posterior margin of each hemelytron and does not contact the other at rest, and the membrane is not reduced with the vein roundly angled in the central area.</p></div>	https://treatment.plazi.org/id/462987920846DB04FED7FCE0FE6937BE	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.		Plazi	Mingheti, Eugenia;Montemayor, Sara Itzel;Dellapé, Pablo Matías	Mingheti, Eugenia, Montemayor, Sara Itzel, Dellapé, Pablo Matías (2025): Phylogenetic revision of the Neella-Neoneella complex (Hemiptera: Heteroptera: Miridae: Bryocorinae), with description of five new genera. Zoological Journal of the Linnean Society 204 (2), DOI: 10.1093/zoolinnean/zlaf043, URL: https://doi.org/10.1093/zoolinnean/zlaf043
462987920847DB04FEC5F8A3FAA232F5.text	462987920847DB04FEC5F8A3FAA232F5.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Paraneella Carvalho 1954	<div><p>Paraneella Carvalho, 1954b</p><p>(Fig. 1B)</p><p>Tope species: Paraneella amazonica Carvalho, 1954b . By monotypy and original designation.</p><p>Paraneella Carvalho, 1954b: 100–101 (original description, fig.); Carvalho, 1957: 119 (catalogue); Carvalho, 1960: 49 (key); Carvalho and Froeschner, 1987: 133 (list); Carvalho and Ferreira, 1995: 477 (key); Schuh, 2002–13 (online catalogue); Mingheti et al., 2023: 1–9 (redescription, key).</p><p>Discussion: In our analysis Paraneella is recovered as monophyletic supported by 19 synapomorphies: seven continuous characters: relations: eyes height/head height (1:0.033), labrum length/labial segment I length (4:0.063), antennal segment I, length/antennal segment II (6:0.122), antennal fossa length/eye height (7:0.036), labial segment I length/vertex width (8:0.102), claval commissure length/scutellum length (13: 0.218), and cuneus length/anterior cuneal margin width (15:0.16); eight discrete contradictory synapomorphic characters: frons globose (30:1), collar glabrous (44:0), anterior pronotal lobe evidently differentiated from posterior lobe, like a neck (49:1), inner margin of cuneus sinuate (71:1), medial angle of membrane cell acute (77:1) and with its posterior margin slightly concave (79:1), procoxae separated from each other (82:1), and laterals and/or posterior margins of cuneus brown to black (157:1) and four discrete synapomorphic characters: vertex globose (31:3), antennal segment I with distal half wider, abruptly swollen at middle (37:4), setae of pronotum absent (53:0), and base of mesofemur expanded (85:1). For a discussion of the genus see Mingheti et al., 2023.</p></div>	https://treatment.plazi.org/id/462987920847DB04FEC5F8A3FAA232F5	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.		Plazi	Mingheti, Eugenia;Montemayor, Sara Itzel;Dellapé, Pablo Matías	Mingheti, Eugenia, Montemayor, Sara Itzel, Dellapé, Pablo Matías (2025): Phylogenetic revision of the Neella-Neoneella complex (Hemiptera: Heteroptera: Miridae: Bryocorinae), with description of five new genera. Zoological Journal of the Linnean Society 204 (2), DOI: 10.1093/zoolinnean/zlaf043, URL: https://doi.org/10.1093/zoolinnean/zlaf043
462987920847DB07FC0FFC68FC4D321C.text	462987920847DB07FC0FFC68FC4D321C.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Proneella Carvalho 1960	<div><p>Proneella Carvalho, 1960</p><p>(Figs 1G, H, 2H, 5L, N, 6)</p><p>Tope species: Proneella boliviana Carvalho, 1960 . By original designation.</p><p>Proneella Carvalho, 1960: 48, 50–52, 55–59 (original description); Carvalho and Froeschner, 1987: 133 (list); Carvalho and Ferreira, 1995: 470, 472 (key). Schuh, 2002–13 (online catalogue).</p><p>Included species: P. boliviana Carvalho, 1960</p><p>P. peruana Carvalho, 1960</p><p>Diagnosis: Orange to reddish, some specimens with brown to black areas; eyes large and sessile; vertex flat; inner margin of eye at level with lateral margins of collar; labium extending to metacoxae; embolium bent upwards; sexual dimorphism in length of cuneus, males with cuneus more developed and its apex ataining posterior margin of membrane, without contacting each other in resting position, vein of cell angled before middle of membrane; genital capsule with sclerotizations in lef margin; subgenital plate with two projections, one dentated in the right and one in the lef; apex of lef paramere hooked; and seminal duct tapering.</p><p>Redescription: Male. TBL 4.32–6.06; PBL 4.37–5.98; BW 2.30– 2.75. Female. TBL 4.84; PBL 4.56; BW 2.35. Coloration: Head: orange to reddish; eyes black or silver; antennal segments I–II orange to reddish or brown; III, pale yellow to reddish; IV, brown. Torax: pronotum orange to reddish; mesoscutum yellow to reddish; scutellum reddish or blackish; pleura yellow to reddish. Hemelytron: orange to reddish, or yellow to reddish with some reddish or brown areas on corium, clavus and/or cuneus; membrane yellow or blackish; veins yellow to reddish. Legs: coxae, femora, and tibiae orange to reddish, sometimes apex brown; tarsi yellow; claws brown. Abdomen: yellow to orange or reddish to brown reddish. Surface: Shiny; posterior pronotal lobe evenly punctate; head and pronotum with short and recumbent setae; labium with semierect setae; antennal with abundant semierect and sparce erect setae; hemelytra with semierect setae; veins with very short and recumbent setae; pleura and abdomen with semierect setae, longer than dorsal; coxae, trochanters, femora, and tarsi with short and recumbent or semierect setae; femora with dorsal setae as long as ventral; tibiae with abundant recumbent and semierect setae. Structure: Head: more than 2× as wide as long; clypeus not prominent, rounded in lateral view; frons rounded in lateral view; vertex flat, wider than head length; eyes large, more than half of head height, sessile, upper margin ataining dorsal margin of head, inner margin straight, at level with lateral margins of collar; gula very short; antennal segment I straight; II, widened centrally or distally, more than 2.5× as long as I; III, tapering towards apex, thinner than II; IV, straight, thinner than III. Torax: anterior margin of collar concave and posterior margin straight; calli slightly evident, small, separated in central area, ataining or not lateral margins of pronotum; posterior pronotal lobe with shallow lateral depressions before humeral angles; posterior margin straight; mesoscutum exposed or not; scutellum with basal depression. Hemelytron with lateral margins convex in males, less evident in females; embolium bent upwards; medial fracture shorter than half of corium; claval commissure longer than scutellum and half of pronotum length combined; anterior half of medial fracture adjacent to R + M vein, posterior half separated from R + M vein; male with apex of cuneus ataining posterior margin of membrane and not contacting each other with hemelytra in resting position, inner margin concave; females with shorter cuneus, not ataining posterior margin of membrane and not contacting each other; veins angled in middle of membrane and before apex of cuneus. Legs: profemora widened basally; meso- and metafemora straight; metafemora slightly curved; protibiae slightly flatened distally; meso- and metatibiae straight. Male genitalia: Genital capsule shorter than a third of abdomen length; right wall longer than lef; genital opening broad, facing dorsally; dorsal wall reduced, with a projection in lef margin; ventral wall more developed than dorsal; posterior margin convex; subgenital plate with lef and right projections, ventral to parameres insertion, lef one as a short wall and right larger, curved and with two tiny basal teeth. Lef paramere strongly curved, hook-shaped; basal process narrow; body wide; apical process tapering towards curved apex. Right paramere curved; basal process narrow; body wide initially, with basal and broad expansion; apical process narrow. Aedeagus small and simple; phallotheca sclerotized, except base; seminal duct membranous and not folded initially, sclerotized posterior to its distal curvature; extending to apex of phallotheca and beyond it; endosoma sclerotized basally.</p><p>Distribution: Argentina, Bolivia, Colombia, and Peru (Fig. 6).</p><p>Discussion: Carvalho (1960), in the original description of the genus, stated that Proneella is closely related to Adneella, Neella, Neoneella, and Paraneella . In our analysis Proneella is recovered as monophyletic supported by 10 synapomorphies: five continuous characters: relations of claval commissure length/ scutellum length (13: 0.190 –0.196), cuneus length/anterior cuneal margin width (15: 0.165 –0.239) genital capsule length/ abdomen length (16:0.014), genital capsule width/genital capsule height (17:0.096), aedeagus length/genital capsule length (18:0.114), three discrete contradictory synapomorphic characters: eyes without projection (23:0), cuneus sexually dimorphic (68:1), and seminal duct tapering (152:1), and two discrete synapomorphic characters: basal blunt tooth in the right process of the subgenital plate (115:1), and distal extreme of lef paramere hook shaped (138:1). Proneella is recovered as the sister-group of Naelle gen. nov., and this clade is the sister of a group composed of Egerocoris, Laterocavocoris gen. nov., Lelena gen. nov., Neella, Neoneella, and Puncticollus gen. nov. Te GC frequencies indicate a high support due to low contradictory information (Fig. 7).</p><p>Neoneella, as Proneella, has sexual dimorphism in the length of the cuneus but in Neoneella the males have an extremely well-developed cuneus that reaches the posterior margin of the membrane, contacting each other at rest, the membrane is reduced, and the vein of the membrane is straight ataining posterior margin of cuneus.</p></div>	https://treatment.plazi.org/id/462987920847DB07FC0FFC68FC4D321C	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.		Plazi	Mingheti, Eugenia;Montemayor, Sara Itzel;Dellapé, Pablo Matías	Mingheti, Eugenia, Montemayor, Sara Itzel, Dellapé, Pablo Matías (2025): Phylogenetic revision of the Neella-Neoneella complex (Hemiptera: Heteroptera: Miridae: Bryocorinae), with description of five new genera. Zoological Journal of the Linnean Society 204 (2), DOI: 10.1093/zoolinnean/zlaf043, URL: https://doi.org/10.1093/zoolinnean/zlaf043
462987920844DB06FBF2FCC1FAD7365D.text	462987920844DB06FBF2FCC1FAD7365D.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Puncticollus Mingheti & Montemayor & Dellapé 2025	<div><p>Puncticollus gen. nov.</p><p>(Figs 1D, 2I, 4I–L, 8)</p><p>Tope species: Neella rondonia Carvalho, 1985d . By present designation.</p><p>Included species: htp://zoobank.org/ urn:lsid:zoobank. org:pub: 152B12F9-8CDE-496F-9BC1-DF87746A3933 P. anduzeei (Carvalho, 1954a), comb. nov.</p><p>P. rondonia (Carvalho, 1985d), comb. nov.</p><p>P. sp 1 sp. nov.</p><p>Diagnosis: Small, TBL less than 4.50 mm; eyes large and stylate, upper margin ataining dorsal margin of head; frons globose in lateral view; labium extending to mesocoxae, labial segment I shorter than vertex; antennal segment I with only short and recumbent setae, tapering towards apex, wider than II; collar punctate; humeral angles separated from central area of posterior pronotal lobe by a deep depression; pro- and metafemora widened basally; aperture of genital capsule small; right process of subgenital plate larger than lef and divided in two branches; right paramere larger than lef; phallotheca completely sclerotized; and females with subgenital plate longer than wide.</p><p>Description: Male. TBL 3.67–4.11; PBL 3.29–3.65; BW 1.41– 1.68. Female. TBL 3.38–4.09; PBL 3.24–3.57; BW 1.5–1.82. Coloration: Head: yellow whitish to orange; eyes golden, silver, black or black with silver areas; antennal segment I yellow whitish to orange; II, orange to brown; III–IV whitish or brown with base whitish. Torax: pronotum, mesoscutum, and scutellum yellow whitish to orange; pleura yellow whitish to orange, in some specimens propleura bicoloured. Hemelytron: yellow whitish to orange; membrane translucent to yellow; veins yellow whitish to orange. Legs: yellow whitish to orange; tarsi pale yellow; claws brown. Abdomen: yellow whitish to orange. Surface: Shiny; collar and posterior pronotal lobe punctate; pronotum, scutellum, and hemelytra with short, recumbent setae; labium with semierect setae; antennal segments I–II with short, recumbent setae; III–IV, with semierect setae; veins with tiny, recumbent setae; pleura and abdomen with semierect setae, longer and more disperse setae than dorsal; coxae, trochanters, and tarsi with short, semierect setae; femora with dorsal setae shorter than ventral. Structure: Head: at least 2× as long as wide; clypeus not prominent, flat to rounded in lateral view; frons globose and prominent in lateral view; vertex flat; eyes large, more than half of head height, stylate and upper margin ataining dorsal margin of head, inner margin at level with lateral margins of collar; maxillary plates mediumsize to large, broad; gula not visible to short; antennal segment I tapering towards apex; II, straight, thinner and more than 2.5× as long as I; III, tapering towards apex; IV, straight. Torax: anterior margin of collar concave and posterior margin convex, wider than antennal segment I; calli not evident to prominent, not connected medially or connected anteriorly, ataining to lateral margins of pronotum; humeral angles separated from central area of posterior pronotal lobe by a deep depression; posterior pronotal margin straight; mesoscutum exposed or not; scutellum flat or with basal depression. Hemelytron: flat, lateral margins convex; embolium thin, flat, bent upwards; anterior half of medial fracture adjacent to R + M vein, posterior half separated from R + M vein; R + M extending to cuneal fracture; claval commissure longer or shorter than scutellum and half of pronotum length combined; cuneus longer than wide, inner margin concave with apex truncate; veins angled in medial area of membrane and before apex of cuneus; inner margin of cell straight or convex and posterior margin straight. Legs: pro- and metafemora widened basally; mesofemora straight; metafemora slightly curved; protibiae flatened distally, meso- and metatibiae straight. Male genitalia: Genital capsule longer than one third of abdomen length, wider than long; genital aperture small and facing caudally; right wall longer than lef; posterior margin of dorsal wall concave; ventral wall more developed than dorsal, posterior margin convex; subgenital plate with two processes, lef smaller and straight, and right larger and divided in two branches, one directed interiorly and the other exteriorly; supragenital bridge present or absent. Lef paramere smaller than right, curved; basal process narrow; body straight or with slight constriction before apical process; apical process tapering. Right paramere curved, wider than lef; basal process narrow; body wide, in some species with projections; apical process reduced to well developed. Aedeagus small and simple; phallotheca sclerotized; seminal duct widened basally, not folded, sclerotized posterior to its distal curvature, ataining at least apex of phallotheca; endosoma completely sclerotized or only on distal half.</p><p>Distribution: Argentina, Brazil, Ecuador, and Venezuela (Fig. 8).</p><p>Etomologo: Te generic name refers to the punctate collar and it is formed by the combination of the Latin words ‘ puncti ’ (points) and ‘ collus ’ (neck). Te gender is masculine.</p><p>Discussion: Puncticollus gen. nov. includes two species transferred from Neella, N. anduzeei and N. rondonia, and a new as yet undescribed species. In our analysis it is recovered as the sister-group of Neoneella and is supported by 15 synapomorphies: six continuous characters:the total length (0:0.473) and the relations, clypeus length/head height (3: 0.039 –0.041), labial segment I length/vertex width (8: 0.077 –0.096), labial segment II/total labial length (9:0.025), cuneus length/anterior cuneal margin width (15: 0.147 –0.148), and female subgenital plate length/anterior margin width (19: 0.172 –0.213); and nine discrete contradictory synapomorphies: upper margin of eyes achieving the head dorsal margin (20:0), frons globose (30:1), antennal segment I with one type of setae (35:1), labium ataining mesocoxae (40:1), humeral angles separated from posterior pronotal lobe by a deep longitudinal depression (52:1), metafemora expanded at base (86:1), genital capsule with a reduced opening (110:1), phallotheca completely sclerotized (145:2), and female subgenital plate truncate (153:2). Te GC frequencies indicate a high support due to low contradictory information (Fig. 7).</p><p>Puncticollus gen. nov. runs to the couplet 8 in the key to the Neotropical eccritotarsine genera (Carvalho and Ferreira 1995), where Hesperolabops and Aztecarina are identified. Puncticollus gen. nov. can be distinguished from the two aforementioned genera by the slightly stylate eyes, the pronotum not strongly narrowed or constricted anteriorly and with the posterior margin straight, and the hemelytra impunctate and yellowish white to orange.</p><p>Tomasomiris Mingheti et al., 2024</p><p>Tope species: Tomasomiris setosus Mingheti et al., 2024 . By monotypy and original designation.</p><p>Tomasomiris Mingheti et al., 2024: 2–4 (original description; figs).</p><p>Discussion: Tis genus was recently described to include the type species from Panama. Tomasomiris is recovered at the base of the clade including Caulotops, Pachopoda, Proneella, Naelle gen. nov., Neella, Laterocavocoris gen. nov., Lelena gen. nov., Egerocoris, Puncticollus gen. nov., and Neoneella . It is supported by 16 synapomorphies. Seven continuous characters: the total length (0: 0.655 –0.666), and the relations: labrum length/labial segment I length (4: 0.018 –0.030), antennal segment I, length/ antennal segment II (6: 0.438 –0.453), scutellum, anterior margin width/scutellum length (12: 0.119 –0.126), corium, medial fracture length/corium length (14: 0.008 –0.009), cuneus length/anterior cuneal margin width (15: 0.096 –0.100) and female subgenital plate length/anterior margin width (19: 0.026 – 0.055); and nine discrete contradictory synapomorphic characters: eyes projected anteriorly (24:2), posterior margin of pronotum convex (51:0), hemelytra with erect setae (62:2), membrane cell with medial angle acute (77:1) and with its posterior margin slightly concave (79:1), calli of pronotum of different coloration than posterior pronotal lobe (154:0), hemelytra with a black central spot (156:1), cuneus with laterals and/or posterior margins brown to black (157:1) and distal extreme of femora with a brown to black dorsal spot (159:1). For a detailed discussion of the genus see Mingheti et al., 2024.</p></div>	https://treatment.plazi.org/id/462987920844DB06FBF2FCC1FAD7365D	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.		Plazi	Mingheti, Eugenia;Montemayor, Sara Itzel;Dellapé, Pablo Matías	Mingheti, Eugenia, Montemayor, Sara Itzel, Dellapé, Pablo Matías (2025): Phylogenetic revision of the Neella-Neoneella complex (Hemiptera: Heteroptera: Miridae: Bryocorinae), with description of five new genera. Zoological Journal of the Linnean Society 204 (2), DOI: 10.1093/zoolinnean/zlaf043, URL: https://doi.org/10.1093/zoolinnean/zlaf043
