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Compsibidion vandenberghei Heffern, Santos-Silva & Nascimento, 2018 (Figs 30–35) Compsibidion vandenberghei Heffern, Santos-Silva & Nascimento, 2018: 526. Compsibidion vandenberghei was described based on two females from Nicaragua (Nueva Segovia) (Heffern et al. 2018). We examined another female from Guatemala (Fig. 30), and in comparison with the type material (holotype illustrated in Figs 31, 33 and 35), the female examined has the body slightly wider, scape shorter and stouter (Fig. 32), flagellomeres slightly thicker, femora slightly thicker, yellowish lateral macula on the anterior third of the elytron closed adjacent to the epipleura (it is open in the holotype), black anterior elytral macula closer to the black transverse band (Fig. 30), transverse black macula on posterior half of the elytron arched upward close to suture (Fig. 30), and procoxal cavities slightly open behind (it is closed in the holotype). However, these types of variations also occur in other species of Compsibidion, as for example, in C. vanum (Thomson, 1867). Additionally, the upper eye lobes (Fig. 34) in the female from Guatemala have three rows of ommatidia, while in the holotype they have four rows (Fig. 35). However, in the female paratype, the left upper eye lobe has four rows of ommatidia, with a single ommatidium in the fourth row, and the right upper eye lobe has three rows of ommatidia. Material examined. GUATEMALA (new country record), Zacapa: Quarry rd to San Lorenzo, Sierra las Minas, 15.043871, -89.668775, 555 m, 1 female, 29-31.V.2019, Skillman, Wappes & Monzón leg. (FWSC). NICARAGUA, Nueva Segovia: Cerro Jesus (1300 m), holotype and paratype female, 25–30.V.2011, E. van den Berghe col. (MZSP; DHCO).

Corimbion wappesi sp. nov. (Figs 6–12) Description. Holotype male (Figs 6–11). Integument mostly black; palpomeres reddish brown, except apex of maxillary palpomeres I–III and labial palpomeres I–II yellowish brown; scape, pedicel, and antennomeres III–VI dark brown (slightly lighter toward VI); antennomeres VII–XI brown (gradually lighter toward XI). Elytra brown, lighter toward posterior fifth; with wide, transverse yellowish-brown band before middle, from suture to epipleural margin, oblique, gradually narrowed near suture. Femoral peduncle dark reddish brown and femoral club dark brown. Tibiae mostly dark reddish brown, more dark brown depending on light intensity. Tarsi dark reddish brown. Apex of ventrites 3–4 narrowly paler; ventrite 5 dark brown basally, gradually reddish brown toward apex. Head. Frons finely, densely rugose and punctate; with abundant, decumbent yellowish pubescence not obscuring integument (pubescence paler depending on light intensity). Area between antennal tubercles and upper eye lobes with sculpturing and pubescence as on frons; with a few long, erect light yellowish-brown setae interspersed close to eyes. Remaining surface of vertex transversely rugose-punctate, with a few short, decumbent yellowish setae. Area behind upper eye lobes finely, abundantly punctate close to eye, punctures coarser and shallower close to prothorax; with abundant yellowish pubescence not obscuring integument (pubescence paler depending on light intensity), glabrous close to prothorax; with a few long, erect light yellowish-brown setae close to eye. Area behind lower eye lobes tumid close to eye; with sculpturing as behind upper eye lobes, except smooth area adjacent to tumid area; pubescence as behind upper eye lobes, sparser superiorly; with long, erect, moderately abundant light yellowish-brown setae on tumid area. Genae finely rugose-punctate, except smooth apex; with sparse yellowish pubescence and a few long, erect setae of same color, except glabrous apex. Wide central area of postclypeus with bristly yellowish pubescence not obscuring integument (pubescence paler depending on light intensity), and one long, erect yellowish seta on each side; sides of postclypeus glabrous. Labrum coplanar with anteclypeus at posterior half, inclined at anterior half; with long, erect yellowish-brown setae on posterior half, longer laterally, and fringe short, erect yellowish-brown setae on anterior half. Gulamentum smooth, glabrous on posterior half; transversely striatepunctate on anterior half, with sparse yellowish pubescence interspersed with long, erect setae of same color. Upper eye lobes with three rows of ommatidia; distance between upper eye lobes 0.39 times distance between outer margins of eyes; in frontal view, distance between lower eye lobes 0.46 times distance between outer margins of eyes. Antennae 2.6 times elytral length, reaching elytral apex at posterior third of antennomere VII. Scape subcylindrical, not sulcate dorsally; finely, abundantly punctate, with some sparse and coarse piliferous punctures interspersed, except smooth apex (smooth area wider on outer region); with moderately abundant yellowish pubescence not obscuring integument, and long, erect yellow setae interspersed, except glabrous smooth area. Pedicel finely, sparsely punctate, except coarser piliferous punctures apically; with sparse yellowish pubescence, and long, erect, moderately abundant yellow setae apically. Antennomere III tumid (Fig. 11), coarsely, sparsely punctate; finely carinate dorsally, from base near apex (carina placed close to inner margin); with abundant yellowish-white pubescence not obscuring integument on part of basal third of dorsal surface and entire outer side, very sparse on remaining surface; with long, erect yellow setae throughout, longer, more abundant ventrally. Antennomeres IV–VI tumid, with yellowish-white pubescence not obscuring integument, abundant dorsally and sparser ventrally; with abundant, long, erect yellow setae ventrally and apically; with dorsal carina from base near apex, less distinct on posterior half of IV. Antennomeres VII–XI slender; with abundant yellowish-white pubescence; VII–X with a few long yellowish setae on apex. Antennal formula based on length of antennomere III: scape = 0.52; pedicel = 0.11; IV = 0.72; V = 0.89; VI = 0.87; VII = 0.85; VIII = 0.80; IX = 0.74; X = 0.69; XI = 0.76. Thorax. Prothorax distinctly longer than wide; anterior and posterior constrictions well-marked; sides rounded centrally. Pronotum densely rugose on anterior and posterior third, and laterally, somehow smooth on center; with one distinct conical tubercle on each side, placed slightly before middle, and another elongated, less elevated placed centrally, from middle to posterior third; with a few coarse punctures on anterior third; with dense pubescence partially obscuring integument, yellowish-white basally, lighter toward its apex, except glabrous tubercles and area surrounding them, and band of sparse pubescence on each side of central tubercle (wide central area mostly glabrous); with long, erect, sparse yellowish-brown setae from anterior margin to before middle, setae yellowish-brown basally, pale yellow toward its apex. Sides of prothorax with a few coarse punctures, except transversely striate area close to anterior margin; with abundant yellowish-white pubescence partially obscuring integument, except glabrous anterior region (this area gradually widened toward prosternum) and posterior region; with long, erect, sparse setae, yellowish-brown basally, pale toward its apex. Prosternum transversely striate on anterior half; with abundant yellowish-white pubescence on posterior half, sparser than on sides of prothorax and a few short setae of same color on anterior half. Prosternal process with abundant yellowish-white pubescence except glabrous sides of apex; narrowest area 0.16 times procoxal width. Procoxal cavities slightly open behind (Fig. 10). Ventral surface of mesothorax with yellowish-white pubescence, denser on anterocentral area of mesoventrite, mesanepisternum and mesepimeron. Metanepisternum and sides of metaventrite with abundant yellowish-white pubescence not obscuring integument; central area of metaventrite with sparse yellowish-white setae anteriorly, glabrous on remaining surface; metaventrite with a few long, erect light yellowish-brown setae. Scutellum with pale yellow pubescence not obscuring integument. Elytra. Coarsely, sparsely punctate on anterior half, punctures finer on posterior half; with sparse yellowish-white pubescence on posterior quarter, reaching posterior third on sides; with long, erect light yellowish-brown seta on nearly all punctures; apex slightly obliquely truncate, with outer and sutural angle rounded, slightly projected. Legs. Femora with abundant grayish-white pubescence not obscuring integument, except glabrous ventral surface of profemora, and glabrous ventral surface of posterior 2/3 of meso- and metafemoral club; with long, erect, sparse light yellowish-brown setae. Protibiae with abundant yellowish-white pubescence, not obscuring integument, dorsally and laterally, and bristly yellowish-brown pubescence ventrally; meso- and metatibiae with sparse yellowish-white pubescence dorsally and laterally, and bristly light pale yellow pubescence on ventral surface of posterior half (yellow pubescence more abundant toward apex); with long, erect, sparse pale yellow setae; meso- and metatibiae longitudinally carinate laterally. Metatarsomere I slightly longer than II–III together. Abdomen. Ventrites with abundant yellowish-brown pubescence not obscuring integument, except almost glabrous area on center of ventrite 1, posterocentral area of ventrite 2, and apex of ventrites 3–4; with long, erect, sparse light yellowish-brown setae, gradually more abundant toward ventrite 5. Female (Fig. 12). It differs from male by the shorter antennae, 2.1 times elytral length, reaching elytral apex at basal area of antennomere IX, and antennomeres III–VI not tumid. Variation. Central tubercle of pronotum as elevated as lateral tubercles; pronotal pubescence light yellowishbrown; pronotal erect setae reaching posterior constriction and partially brownish. Dimensions (mm) (Holotype male/ paratypes male/ paratypes female). Total length, 9.95/7.55–9.70/9.05–12.20; prothoracic length, 2.20/1.75–2.10/1.95–2.65; anterior prothoracic width, 1.40/1.10–1.30/1.20–1.65; posterior prothoracic width, 1.35/1.05–1.25/1.10–1.60; maximum prothoracic width, 1.50/1.20–1.40/1.25–1.80; humeral width, 2.00/1.60–1.85/1.65–2.40; elytral length, 6.10/4.70–5.55/5.45–7.20. Type material. Holotype male from GUATEMALA, Zacapa: El Arenal, Heloderma Conservation Reserve, 14º18’N, 89º78’W, 530 m, collected at MV/UV lights, 23-15.V.2019, Wappes, Monzón & Skillman leg. (FSCA, formerly ACMT). Paratypes — GUATEMALA, Zacapa: 1 male, same data as holotype (FSCA, formerly ACMT); 1 male, 1 female, same data as holotype, except Skillman, Wappes & Monzón leg. (FWSC); Quarry Rd to San Lorenzo, Sierra Las Minas, 15º04’N, 89º67’W, 555 m, MV/UV lights, 1 male, 26.V.2019, Wappes, Monzón & Skillman leg. (MZSP, formerly ACMT); 500-600 m, MV/UV lights, 1 female, 26.V.2019, Wappes, Monzón & Skillman leg. (MZSP, formerly ACMT). Etymology. The specific epithet “ wappesi ” is in honor to the late James Wappes, in recognition of his contributions to the knowledge of Cerambycidae. Remarks. Depending on the feature and/or the interpretation of the features, the new species can be included in Compsibidion (Neoibidionina), Corimbion, Pygmodeon or Heterachthes (Compsina). Only a complete review of these genera may present reliable features to separate them or, eventually, to propose synonymies. This is because the features used to separate them are too variable in the genera studied: basal antennomeres carinate or not (Compsibidion and Heterachthes), central tubercle of the prothorax elevated or not (variable in Heterocompsa and Corimbion) procoxal cavities closed or slightly open behind (at least variable in Corimbion, Compsibidion and Pygmodeon), tibiae with or without carina (at least variable in Compsibidion and Heterachthes), presence of pubescent band on sides of the prothorax (at least variable in Compsibidion and Heterachthes), etc. For now, we think better to include the new species in Corimbion. By the elytral pattern, the new species cannot be confused with any species currently included in Corimbion. This is because there are no other species with only a transverse yellowish band about middle, and no other macula anterior and/or posterior to it., Published as part of García, Kimberly & Santos-Silva, Antonio, 2022, New species and new records in Neoibidionini and Hexoplonini (Coleoptera: Cerambycidae: Cerambycinae), pp. 399-414 in Zootaxa 5134 (3) on pages 401-404, DOI: 10.11646/zootaxa.5134.3.4, http://zenodo.org/record/6538351

Neocompsa pilosa sp. nov. (Figs 13–18) Description. Holotype male (Figs 13–17). Head brown dorsally, dark reddish brown laterally and ventrally, reddish brown on frons and antennal tubercles; apex of palpomeres pale yellow; antennae and legs reddish brown. Prothorax and ventral surface of meso- and metathorax dark reddish brown, darker than on dorsal surface of head, with lighter irregular areas. Elytra dark reddish brown basally, gradually lighter toward apex, except yellowish-white longitudinal band dorsally, from anterior quarter to slightly after middle. Ventral surface of abdomen brown basally, gradually orangish brown toward ventrite 5. Head. Frons finely, densely rugose-punctate; with sparse straw-colored pubescence, denser close to clypeus. Antennal tubercles smooth, almost glabrous, elevated and abruptly inclined posteriorly. Vertex and area behind upper eye lobes finely, densely rugose-punctate; with straw-colored pubescence not obscuring integument, denser close to lower eye lobe, and long, erect light yellowish-brown setae interspersed close to eyes. Area behind lower eye lobes tumid close to eye; coarsely, shallowly punctate on tumid area, almost smooth close to prothorax; with a few short, decumbent straw-colored setae on tumid area, absent close to prothorax, and long, erect light yellowish-brown setae on tumid area (erect setae more abundant than behind upper eye lobes). Genae finely rugose-punctate; with sparse straw-colored pubescence. Wide central area of postclypeus with abundant, bristly straw-colored pubescence not obscuring integument, and one long, erect yellowish-brown seta on each side; sides of postclypeus glabrous. Labrum coplanar with anteclypeus at posterior third, inclined at anterior 2/3; with sparse, erect yellowish-brown setae, both short and long, directed forward laterally. Gulamentum smooth, glabrous on posterior half; anterior half transversely striate, with sparse, suberect straw-colored setae, and sparse, long, erect setae, yellowish-brown basally, gradually paler toward apex. Upper eye lobes with three rows of ommatidia (Fig. 17); distance between upper eye lobes 0.31 times distance between outer margins of eyes; in frontal view, distance between lower eye lobes 0.45 times distance between outer margins of eyes. Antennae 2.0 times elytral length, reaching elytral apex at base of antennomere IX. Scape subpiriform; finely, somewhat sparsely punctate, except smooth apex; with sparse yellowish-white pubescence, and long, erect yellowish-brown setae interspersed. Pedicel finely punctate except smooth apex; with sparse yellowish-white pubescence and long, erect yellowish-brown setae interspersed. Antennomeres III–VI wide and tumid, decreasing the width toward the VI; with distinct longitudinal carinae dorsally and ventrally; with sparse, straw-colored pubescence, almost absent on entire inner surface of III–V; with long, erect yellowish-brown setae, longer ventrally, more abundant especially on III–V.Antennomeres VII–XI cylindrical; with abundant yellowish-white pubescence; VII–X with long, erect yellowish-brown setae apically, longer ventrally. Antennal formula based on length of antennomere III: scape = 0.44; pedicel = 0.14; IV = 0.53; V = 0.78; VI = 0.78; VII = 0.64; VIII = 0.61; IX = 0.55; X = 0.50; XI = 0.58. Thorax. Prothorax cylindrical, distinctly longer than wide; sides slightly narrowed close to posterior sixth. Pronotum coarsely, sparsely punctate, punctures slightly more abundant laterally, almost smooth centrally; sides with dense, wide straw-colored pubescent band; central area with sparse straw-colored pubescence close to anterior and posterior margins (denser on posterior margin); with long, erect, sparse yellowish-brown setae. Sides of prothorax coarsely, sparsely punctate, except transversely striate area close to anterior margin (this area gradually widened toward prosternum); with dense straw-colored pubescent band close to prosternum and posterior margin, not reaching striate anterior area; remaining surface almost glabrous. Prosternum finely, sparsely punctate about posterior half, transversely striate on remaining surface; with sparse yellowish-white pubescence on posterior third, except dense pubescence close to procoxal cavities, a few short, decumbent setae of same color centrally, glabrous anteriorly. Prosternal process with yellowish-white pubescence not obscuring integument; narrowest area 0.15 times procoxal width. Ventral surface of meso- and metathorax with yellowish-white pubescence not obscuring integument, slightly denser on inferior area of mesanepisternum, mesepimeron, and sparser on part of mesoventrite. Mesoventral process distinctly widened posteriorly; maximum width 0.85 times mesocoxal width. Scutellum with dense straw-colored pubescence. Elytra. Coarsely, abundantly punctate on anterior half, except fine and sparse punctures on yellowish-white band, punctures finer, distinctly sparer on posterior half; with short yellowish-white seta within nearly all punctures on anterior half, except sides from anterior third with dense yellowish-white pubescence not obscuring integument; and long, erect, sparse yellowish-brown setae throughout, denser on lateral sides of apical fourth; apex obliquely truncate, slightly emarginate, with outer angle projected. Legs. Femora with yellowish-white pubescence not obscuring integument, absent on ventral surface of femoral club and mostly of outer surface of profemora and ventral surface of meso- and metafemora; with long, erect, sparse yellowish-brown setae interspersed; outer apex of meso- and metafemora with short, fine longitudinal carina. Tibiae with abundant yellowish-white pubescence not obscuring integument, except bristly yellowish-brown pubescence on posterior third of ventral surface; with long, erect yellowish-brown setae interspersed. Tarsomeres with yellowish-white pubescence not obscuring integument, and long, erect yellowish-brown setae interspersed; metatarsomere I about as long as II–III together. Abdomen. Ventrites with abundant yellowish-white pubescence not obscuring integument, and a few long, erect yellowish-brown setae interspersed; apex of ventrite 5 emarginate. Female (Fig. 18). It differs from male by the shorter antennae, 1.9 times elytral length, reaching elytral apex at apex of antennomere IX. Apex of ventrite 5 truncate, slightly emarginate centrally. Variation. The paratype female has part of the yellowish-white band surrounded by dark brown. Dimensions (mm) (Holotype male/ paratype female). Total length, 8.05/6.80; prothoracic length, 1.90/1.50; anterior prothoracic width, 1.00/0.80; posterior prothoracic width, 0.95/0.80; maximum prothoracic width, 1.05/0.90; humeral width, 1.35/1.20; elytral length, 5.00/4.10. Type material. Holotype male from PARAGUAY, Itapúa: Hotel Tirol, 27º11’00”S, 55º50’42”W, 827 ft., 25- 26.II.2019, J.E. Eger & L. Bezark leg. (FSCA, formerly RFMC). Paratype female, same data as holotype (RFMC). Etymology. Latin “pilosus”, meaning hairy, referring to the abundant setae on the antennae, elytra, and legs. Remarks. Neocompsa pilosa sp. nov. differs from N. aspasia Martins, 1974 as follows: antennomeres unicolorous; pronotum with dense pubescent band laterally; elytra with one longitudinal yellowish-white band; elytra with dense pubescence on posterior half; elytral apex obliquely truncate with outer angle projected. In N. aspasia, the antennomeres V–XI are bicolorous; pronotal pubescence is sparse laterally, elytra with two longitudinal yellowish bands, sparse pubescence on posterior half, and rounded apex. The new species is also similar to N. albopilosa (Martins, 1962), N. tucumana (Martins, 1962), N. serrana (Martins, 1962), N. vogti Martins, 1970, and N. lineolata (Bates, 1870), especially by having a single longitudinal yellowish band on each elytron, but it differs by the pronotum with dense lateral pubescence (absent in these species). Also, it differs from N. serrana and N. vogti by having dense pubescence only on apical half of the elytra (elytral pubescence is present throughout in N. serrana and N. vogti). Lastly, the new species is similar to N. santarensis Martins & Galileo, 1998 by having sparse pubescence only on the posterior half of the elytra; however, it differs from N. santarensis by having a single longitudinal band on each elytron (N. santarensis has two bands, one of them elliptical). In the key to species of Neocompsa from Martins (2009), the new species can be included in the alternative of couplet “10,” modified: 10(9). Elytra pubescent on posterior half, glabrous or almost glabrous on anterior half..................................10’ - Elytra almost entirely pubescent....................................................................... 11 10’(10). Pronotum with dense pubescent band laterally; elytra with one longitudinal yellowish band, and with dense pubescence on posterior half. Paraguay.................................................................. N. pilosa sp. nov. - Pronotum without dense pubescent band laterally; elytra with two yellowish bands, one longitudinal anteriorly, another rounded posteriorly, and with sparse pubescence on posterior half. Brazil (Pará)...................................................................................................... N. santarensis Martins & Galileo, 1998, Published as part of García, Kimberly & Santos-Silva, Antonio, 2022, New species and new records in Neoibidionini and Hexoplonini (Coleoptera: Cerambycidae: Cerambycinae), pp. 399-414 in Zootaxa 5134 (3) on pages 404-407, DOI: 10.11646/zootaxa.5134.3.4, http://zenodo.org/record/6538351, {"references":["Martins, U. R. (2009) Tribo Ibidionini, Subtribo Compsina. In: Martins, U. R. (Org.), Cerambycidae Sul-Americanos (Coleoptera). Volume 10. Sociedade Brasileira de Entomologia, Sao Paulo, pp. 1 - 199."]}

Heterachthes boliviensis sp. nov. (Figs 24–29) Description. Holotype female. Head capsule reddish brown, dark orangish-brown ventrally and on antennal tubercles; ventral mouthparts dark orangish brown, except pale yellow apex of palpomeres; scape orangish brown, except irregular brownish area near dorsal apex; pedicel orangish brown, lighter toward apex; antennomeres III–XI orangish, slightly darkened on apex of III–X; mandibles orangish-brown, except dark brown margins and almost black apical third. Prothorax dark reddish brown, except brown anterior and posterior margins and area surrounding procoxal cavities. Ventral surface of mesothorax mostly reddish brown, except orangish posterocentral area of mesoventrite, central area of mesoventral process, and brownish margins of mesanepisternum, mesepimeron, and mesoventral process. Metanepisternum reddish brown; metaventrite dark orangish brown anteriorly and laterally, light orangish brown on wide central area, and yellowish close to metacoxal cavities. Elytra brownish on anterior seventh, with two yellowish maculae on each elytron, the anterior one from anterior seventh to slightly after middle, almost reaching epipleural margin and suture; the posterior one smaller, reaching epipleural margin and suture, with its anterior and posterior margins sinuous; with brown transverse macula separating yellowish maculae. Coxae mostly orangish brown; trochanters mostly light orangish brown; femoral peduncle pale yellow; femoral club brownish, except yellowish-brown apex; tibiae orangish-brown basally, pale yellow on remaining surface; tarsi light orangish brown, slightly brownish on apex of tarsomeres I–II. Ventral surface of abdomen reddish brown, except pale yellow apical margin of ventrites 1–4. Head. Frons finely rugose-punctate; sides of frontal-plate rounded and slightly inclined upward; with distinct sulcus between sides of frontal-plate and lower eye lobes, curved toward anterocentral region; with sparse whitish pubescence, almost absent on central area of frontal-plate. Antennal tubercles moderately elevated and abruptly inclined posteriorly; finely punctate, except smooth apex; with whitish pubescence not obscuring integument. Area between tubercles, finely, abundantly punctate, punctures confluently close to tubercles, and U-shaped sulcus close to anterior margin of upper eye lobes; with sparse whitish pubescence. Vertex finely, sparsely punctate; with slightly, transversely rugose area close to prothorax; and sparse yellowish-white pubescence, almost absent close to prothorax, and one long, erect yellowish seta on each side near eyes. Area behind upper eye lobes smooth close to eye, slightly rugose close to prothorax; with yellowish-white pubescence superiorly close to eye, glabrous on remaining surface. Area behind lower eye lobes finely, sparsely punctate close to eye, smooth close to prothorax; with short, decumbent, very sparse yellowish-white setae on inferior half close to eye, and long, erect yellowish setae on posterior 2/3 close to eye. Genae finely, abundantly punctate, except smooth apex; with whitish pubescence not obscuring integument, absent on smooth apex, and a few long, erect whitish setae toward ventral surface. Wide central area of postclypeus with bristly whitish pubescence not obscuring integument, and one long, erect seta of same color on each side; sides of postclypeus smooth, glabrous. Labrum coplanar with anteclypeus at posterior 2/3, inclined at anterior third; finely, sparsely punctate and with a few short, bristly whitish setae on anterior area of coplanar area; with abundant, bristly whitish pubescence on inclined area, and a few long, erect setae of same color interspersed. Basal 2/3 of outer surface of mandibles rugose-punctate; with sparse whitish pubescence and a few long, erect yellowish-brown setae interspersed; apical third smooth, glabrous. Gulamentum smooth, glabrous on posterior half; anterior half slightly depressed, transversely rugose-punctate, with short, sparse, decumbent yellowish-white setae, denser close to anterior margin, and a few long, erect setae of same color interspersed. Upper eye lobes with two rows of ommatidia, with a single ommatidium near inner apex (Fig. 29); distance between upper eye lobes 0.38 times distance between outer margins of eyes; in frontal view, distance between lower eye lobes 0.48 times distance between outer margins of eyes. Antennae 1.9 times elytral length, reaching elytral apex at base of antennomere IX. Scape subcylindrical, arched in lateral view; finely, sparsely punctate, except smooth apex of dorsal surface; with sparse minute yellowish-white pubescence, absent on smooth area, and a few long, erect yellowish-white setae. Pedicel and antennomeres III–XI with abundant whitish pubescence not obscuring integument; pedicel and antennomeres III–V with long, erect, sparse yellowish-white setae ventrally (sparser toward V) and moderately long, erect, sparse yellowish-white setae on dorsal apex; antennomeres VI–X with moderately short, erect, sparse yellowish-white setae on ventral apex. Antennal formula based on length of antennomere III: scape = 0.57; pedicel = 0.17; IV = 0.72; V = 0.87; VI = 0.87; VII = 0.83; VIII = 0.77; IX = 0.73; X = 0.62; XI = 0.73. Thorax. Prothorax longer than wide; anterior and posterior constrictions distinct, especially the posterior one; sides slightly rounded between constrictions. Pronotum with five, slightly elevated gibbosities, one subrounded on each side of anterior third; one subrounded, almost indistinct, on each side of posterior third; and another longitudinal, more conspicuous, centrally; finely, sparsely punctate anteriorly and posteriorly, smooth centrally; with abundant yellowish-white pubescence not obscuring integument, almost absent on wide central area, central and posterolateral tubercles, and T-shaped central area of anterior quarter, with long, erect yellowish-white setae interspersed. Sides of prothorax finely, sparsely punctate, except transversely striate anterior area (this area gradually widened toward prosternum); with abundant yellowish-white pubescence close to pronotum, almost absent toward prosternum; with a few long, erect yellowish-white setae superiorly. Prosternum finely, sparsely punctate on sides of posterior half, transversely striate on anterior half, abundantly punctate close to posterior half; in lateral view, distinctly concave centrally; with wide U-shaped yellowish-white pubescent band on posterior half (pubescence slightly denser close to procoxal cavities), almost glabrous on remaining surface. Narrowest area of prosternal process 0.12 times procoxal width. Ventral surface of mesothorax with abundant yellowish-white pubescence not obscuring integument, sparser on posterocentral area of mesoventrite and mesoventral process; posterocentral area of mesoventrite gradually, distinctly elevated toward mesoventral process. Mesoventral process distinctly widened posteriorly; widest area 0.9 times mesocoxal width. Scutellum with sparse whitish pubescence not obscuring integument. Elytra. Coarsely, sparsely punctate; with short, decumbent, very sparse yellowish-white setae, and long, erect, sparse pale-yellow setae; apex truncate, slightly concave centrally. Legs. Femora with abundant yellowishwhite pubescence not obscuring integument, and long, erect setae of same color interspersed. Tibiae with abundant whitish pubescence not obscuring integument, longer, bristly on ventral surface of posterior third, and long, erect setae of same color interspersed. Metatarsomere I slightly longer than II–III together. Abdomen. Ventrites with abundant whitish pubescence laterally, distinctly sparser centrally on ventrites 1–4, and almost absent on their apex; with a few long, erect yellowish setae interspersed on sides of ventrites 2–5, and apex of ventrite 5; apical margin of ventrite 5 rounded. Dimensions (mm). Total length, 8.05; prothoracic length, 1.60; anterior prothoracic width, 1.05; posterior prothoracic width, 1.05; maximum prothoracic width, 1.15; humeral width, 1.60; elytral length, 5.25. Type material. Holotype female from BOLIVIA, La Paz: Sur Yungas, Carmen Pampa, 5500’, black light trap, 11.XI.1976, L. Janicki leg. (FSCA, formerly RFMC). Etymology. The specific epithet “ boliviensis ” comes from the country Bolivia, where the holotype was collected. Remarks. Heterachthes boliviensis sp. nov. is similar to H. concretus Martins, 1970 (see photographs on Bezark 2022), but differs as follows: upper eye lobes with less than four rows of ommatidia; anterior half of the elytra mostly light yellowish brown; posterior quarter of the elytra entirely light yellowish brown. In H. concretus, the upper eye lobes have four rows of ommatidia; anterior half of the elytra has a yellowish-brown macula near middle; and the posterior third of the elytra has a wide yellowish-brown macula with brown area close to its posterior margin, and the elytral apex is yellowish. The new species is also similar to H. pallidipennis (Thomson, 1865) by having less than four rows of ommatidia. However, it differs by the basal antennomeres not carinate, elytral apex truncate, and elytral surface with four to five rows of piliferous punctures. In H. pallidipennis, the basal antennomeres are carinate, elytral apex is rounded, and the elytral surface has two rows of piliferous punctures. Heterachthes boliviensis sp. nov. can be included in the alternative of couplet “11” from Martins (2009) (translated; modified): 11(8). Upper eye lobes with less than four rows of ommatidia................................................... 11’ - Upper eye lobes with four rows of ommatidia............................................................ 12 11’(11). Elytra with arched dark brown band on anterior half and two rows of erect setae. Chile (?), Peru............................................................................................ H. pallidipennis (Thomson, 1865) - Elytra without arched dark brown band on anterior half, and rows or erect setae more abundant and somewhat irregular. Bolivia (La Paz)................................................................... H. boliviensis sp. nov., Published as part of García, Kimberly & Santos-Silva, Antonio, 2022, New species and new records in Neoibidionini and Hexoplonini (Coleoptera: Cerambycidae: Cerambycinae), pp. 399-414 in Zootaxa 5134 (3) on pages 410-412, DOI: 10.11646/zootaxa.5134.3.4, http://zenodo.org/record/6538351, {"references":["Bezark, L. G. (2022) A photographic Catalog of the Cerambycidae of the World. New World Cerambycidae Catalog. Available from: http: // bezbycids. com / byciddb / wdefault. asp? w = n / (accessed 18 March 2022)","Martins, U. R. (2009) Tribo Ibidionini, Subtribo Compsina. In: Martins, U. R. (Org.), Cerambycidae Sul-Americanos (Coleoptera). Volume 10. Sociedade Brasileira de Entomologia, Sao Paulo, pp. 1 - 199."]}

Gnomidolon incisum Napp & Martins, 1985 (Figs 1–5) Gnomidolon incisum Napp & Martins, 1985: 127; Joly, 1991: 24; Monné, 1993: 13 (cat.); Monné & Giesbert, 1994: 67 (checklist); Monné, 2005: 310 (cat.); Martins, 2006: 147; Monné & Hovore, 2006: 86 (checklist); Monné, 2022: 492 (cat.). Gnomidolon incisum is known only from its type-locality in Venezuela (Napp & Martins 1985). We examined a female specimen from Trinidad and Tobago (Fig. 1). This specimen differs from the type material (paratype illustrated in Fig. 2) by the scape orangish (dark reddish brown in the holotype and paratype), and elytra without dark band projected toward anterior third along suture (present in the holotype and paratype). As there are no morphological structures differentiating the specimens, we concluded these are just chromatic variations. The length of the inner spine of the left metafemur is considerably different in the specimen from Trinidad and Tobago (Fig. 3); however, it varies within the same specimen and, in fact, the length of the inner spine of the right metafemur (Fig. 4) agrees well with that in the paratype of G. incisum (Fig. 5). Therefore, this characteristic is variable intraspecifically. Material examined. TRINIDAD AND TOBAGO (new country record), Trinidad, Tunapuna-Piarco: Saint Augustine, Mount Saint Benedict, Abbey, 1 female, 29.VI.1994, B.K. Dozier leg. (FSCA)., Published as part of García, Kimberly & Santos-Silva, Antonio, 2022, New species and new records in Neoibidionini and Hexoplonini (Coleoptera: Cerambycidae: Cerambycinae), pp. 399-414 in Zootaxa 5134 (3) on pages 400-401, DOI: 10.11646/zootaxa.5134.3.4, http://zenodo.org/record/6538351, {"references":["Napp, D. S. & Martins, U. R. (1985) Ibidionini (Coleoptera, Cerambycidae) Ia. Divisao: notas, chaves e descricoes. Papeis Avulsos de Zoologia, 36 (12), 111 - 130.","Monne, M. A. (2022) Catalogue of the Cerambycidae (Coleoptera) of the Neotropical region. Part I. Subfamily Cerambycinae. Available from: https: // cerambycids. com / catalog / (accessed 18 March 2022)"]}

Four new species are described in Neoibidionini (Compsina): Corimbion wappesi, from Guatemala, Zacapa; Neocompsa pilosa, from Paraguay, Itapúa; Neocompsa soniae, from Panama, Chiriquí; and Heterachthes boliviensis, from Bolivia, La Paz. New country record, Trinidad and Tobago, as well as chromatic and morphological variations are reported to Gnomidolon incisum Napp & Martins, 1985 (Hexoplonini), and Compsibidion vandenberghei Heffern, Santos-Silva & Nascimento, 2018 (Neoibidionini, Neoibidionina). Additionally, a key to species of Corimbion Martins, 1970 are provided, and the two new species of Neocompsa Martins, 1965, and the new species of Heterachthes Newman, 1840 are included in a previous key.

Hamaticherus Dejean, 1821 (Coleoptera: Cerambycidae: Cerambycinae) is considered a junior synonym of Cerambyx Linnaeus, 1758. Hamaticherus sensu Audinet-Serville, 1834 is considered a posterior usage of Hamaticherus Dejean, 1821, and an unavailable name. Plocaederus is considered as a new genus, and not a replacement name, proposed by Dejean (1835) to allocate the species included in Hamaticherus sensu Audinet-Serville, 1834. Therefore, a new genus, Hamaederus Santos-Silva, Garcia and Botero,is herein proposed to include the species currently allocated in Plocaederus Dejean, 1835, creating 15 new combinations, and additionally, a new species from French Guiana, Hamaederus allofasciatus Santos-Silva, Garcia and Botero, is described. Furthermore, Plocaederus barauna Martins and Monné, 2002 and Plocaederus confusus Martins and Monné,2002 are proposed as new junior synonyms of Hamaederus yucatecus (Chemsak and Noguera, 1997), and Hamaticherus bellator Audinet-Serville, 1834 is transferred to Plocaederus Dejean, 1835, new combination. New geographical records are provided for Hamaederus fraterculus (Martins), H. glaberrimus (Martins), H. rusticus (Gounelle), and H. yucatecus (Chemsak and Noguera). Hamaederus fasciatus is formally excluded from the fauna of French Guiana. A key to American genera of Cerambycina (Cerambycini) is provided.

En los próximos años, el uso de catalizadores sigue aumentando, ya que desempeña un papel importante en la fabricación de productos básicos, petroquímicos, químicos, farmacéuticos y alimenticios, además de servir como una herramienta para la mejora el rendimiento de las nuevas tecnologías energéticas. Por otro lado, los procesos de síntesis de catalizadores generan residuos en los laboratorios y fábricas, convirtiéndose en un desafío ambiental debido a su composición particular. En este contexto, se pueden utilizar herramientas como el análisis de ciclo de vida (ACV) para cuantificar los impactos ambientales e identificar los puntos débiles, que deberán ser mitigados. Por lo tanto, en esta revisión, se evaluaron tres catalizadores: Zn, Pd, Pt, al igual que sus impactos ambientales. Finalmente, se encontraron algunos de los usos potenciales en la reducción de las emisiones de gases de efecto invernadero (GEI) y el aumento en el rendimiento de la producción de energía y urea, así como el aumento del rendimiento en el gas total y de hidrógeno; también se consideró el uso de los residuos de base como catalizadores, por ejemplo, en la industria del petróleo y las cenizas generadas durante los procesos de combustión de residuos sólidos urbanos (RSU), neumáticos y carbón, Catalyst use will continue to increase in the coming years, as they are essential in the manufacture of commodities and petrochemicals and chemicals, pharmaceuticals, and foodstuffs, and also serves as a tool for improving the performance of new energy technologies. On the other hand, the synthesis of catalysts generates waste in laboratories and factories, presenting an environmental challenge due to its particular composition. In this context, life cycle analysis (LCA) can quantify environmental impacts and identify areas of vulnerability that should be addressed. As a result, this review evaluated three catalysts: Zn, Pd, and Pt, as well as their environmental impacts. Finally, some possible uses include reducing greenhouse gas (GHG) emissions and increasing energy and urea production yields, as well as total gas and hydrogen yields; the use of base residues as catalysts was also considered, for example, in the petroleum industry and the ashes generated during municipal solid waste (MSW) combustion processes

Sydax gibbus Joly, 1985 Material examined COLOMBIA ��� 1 spec.; Atl��ntico, Usiacur��, Reserva Campesina La Monta��a; 10��46���2.6��� N, 75��0.2���34��� W; 260 m a.s.l.; 12���14 May 2018; K. Garc��a leg; tropical dry forest, light trap; UARC. Geographical distribution Venezuela, Colombia (Bol��var). New department record is added: Atl��ntico (Colombia)., Published as part of Garc��a, Kimberly, Botero, Juan Pablo & Santos-Silva, Antonio, 2021, A new genus of Achrysonini and new records in Cerambycidae (Coleoptera, Chrysomeloidea) from Colombia, pp. 89-109 in European Journal of Taxonomy 735 on page 100, DOI: 10.5852/ejt.2021.735.1243, http://zenodo.org/record/4554780

Jupoata rufipennis (Gory, 1831) Material examined COLOMBIA ��� 1 spec.; Bol��var, San Jacinto, Reserva La Flecha; 09��51���12.4��� N, 75��10���41.4��� W; 324 m a.s.l.; 13���16 Apr. 2018; K. Garc��a leg; tropical dry forest, light trap; UARC. Geographical distribution Mexico, Nicaragua, Costa Rica, Panama, Trinidad and Tobago, Colombia (Amazonas), Venezuela, Ecuador, Surinam, Guyana, French Guiana, Brazil (Roraima, Amazonas, Par��, Mato Grosso, Goi��s, Maranh���o, Cear��, Pernambuco, Bahia, Minas Gerais, Esp��rito Santo, Rio de Janeiro, S���o Paulo, Paran��, Santa Catarina, Rio Grande do Sul), Peru, Bolivia (Cochabamba, La Paz, Santa Cruz), Paraguay, Argentina (Misiones), Uruguay, Honduras, Guatemala. New department record is added: Bol��var (Colombia)., Published as part of Garc��a, Kimberly, Botero, Juan Pablo & Santos-Silva, Antonio, 2021, A new genus of Achrysonini and new records in Cerambycidae (Coleoptera, Chrysomeloidea) from Colombia, pp. 89-109 in European Journal of Taxonomy 735 on page 98, DOI: 10.5852/ejt.2021.735.1243, http://zenodo.org/record/4554780

Phoebe birai Galileo, 2015 Material examined COLOMBIA ��� 1 spec.; Atl��ntico, Usiacur��, Reserva Campesina La Monta��a; 10��46���2.6��� N, 75��0.2���34��� W; 260 m a.s.l.; 12 May 2018; K. Garc��a leg; tropical dry forest, light trap; UARC. Geographical distribution Bolivia (Santa Cruz). A new country record from Colombia (Atl��ntico) is added., Published as part of Garc��a, Kimberly, Botero, Juan Pablo & Santos-Silva, Antonio, 2021, A new genus of Achrysonini and new records in Cerambycidae (Coleoptera, Chrysomeloidea) from Colombia, pp. 89-109 in European Journal of Taxonomy 735 on page 105, DOI: 10.5852/ejt.2021.735.1243, http://zenodo.org/record/4554780

Mimasyngenes icuapara Galileo & Martins, 1996 Material examined COLOMBIA • 1 spec.; Atlántico, Usiacurí, Reserva Campesina La Montaña; 10°46′2.6″ N, 75°0.2′34″ W; 260 m a.s.l.; 12 May 2018; K. García leg; tropical dry forest, light trap; UARC. Geographical distribution Costa Rica, Colombia, Venezuela, Brazil (S„o Paulo), Argentina (Misiones). The species is registered from Colombia but without further locality. Herein, the species is registered from the department of Atlántico (Colombia).

Amphelictus castaneus Chemsak & Linsley, 1964 Material examined COLOMBIA • 1 ♂, 1 ♀; Bolívar, San Jacinto, Reserva La Flecha; 09°51′12.4″ N, 75°10′41.4″W; 324 m a.s.l.; 13–16 Apr. 2018; K. García leg; tropical dry forest, light trap; MZSP. Geographical distribution Venezuela, Colombia (Cundinamarca, Magdalena), Ecuador, French Guiana, Brazil (Amazonas, Goiás), Bolivia (Santa Cruz). New department record is added: Bolívar (Colombia).

Chrysoprasis vittata Aurivillius, 1910 Material examined COLOMBIA ��� 1 spec.; Bol��var, San Jacinto, Reserva La Flecha; 09��51���12.4��� N, 75��10���41.4��� W; 324 m a.s.l.; 13���16 Apr. 2018; K. Garc��a leg; tropical dry forest, UV light trap; UARC. Geographical distribution Venezuela, Colombia (Magdalena, Norte de Santander). New department record is added: Bol��var (Colombia)., Published as part of Garc��a, Kimberly, Botero, Juan Pablo & Santos-Silva, Antonio, 2021, A new genus of Achrysonini and new records in Cerambycidae (Coleoptera, Chrysomeloidea) from Colombia, pp. 89-109 in European Journal of Taxonomy 735 on page 98, DOI: 10.5852/ejt.2021.735.1243, http://zenodo.org/record/4554780

Jupoata robusta Martins & Monné, 2002 Material examined COLOMBIA • 1 spec.; Atlántico, Usiacurí, Reserva Campesina La Montaña; 10°46′2.6″ N, 75°0.2′34″ W; 260 m a.s.l.; 7 Mar. 2018; K. García leg; tropical dry forest, white light trap; UARC. Geographical distribution Brazil (Maranh„o, Pernambuco, Bahia, Goiás, Minas Gerais, Rio de Janeiro, S„o Paulo, Santa Catarina), Costa Rica (Limón). A new country record from Colombia (Atlántico) is added.

Mallodon dasystomus (Say, 1824) Material examined COLOMBIA ��� 1 spec.; Bol��var, San Jacinto, Reserva La Flecha; 09��51���12.4��� N, 75��10���41.4��� W; 324 m a.s.l.; 16 Apr. 2018; K. Garc��a leg; tropical dry forest, UV light trap; UARC. Geographical distribution Southern United States of America, Mexico (Jalisco, Nayarit, Sinaloa, Tamaulipas, Veracruz), Honduras, Tobago, Colombia. The species is registered from Colombia but without any specific locality. Herein, the species is registered from the department of Bol��var (Colombia)., Published as part of Garc��a, Kimberly, Botero, Juan Pablo & Santos-Silva, Antonio, 2021, A new genus of Achrysonini and new records in Cerambycidae (Coleoptera, Chrysomeloidea) from Colombia, pp. 89-109 in European Journal of Taxonomy 735 on page 107, DOI: 10.5852/ejt.2021.735.1243, http://zenodo.org/record/4554780

Hippopsis lemniscata lemniscata (Fabricius, 1801) Material examined COLOMBIA ��� 1 spec.; Atl��ntico, Usiacur��, Reserva Campesina La Monta��a; 10��46���2.6��� N, 75��0.2���34��� W; 260 m a.s.l.; 12���13 May 2018; K. Garc��a leg; tropical dry forest, beating sheet; UARC. Geographical distribution Canada, Eastern United States of America to Texas, Mexico, Guatemala, Honduras, Nicaragua, Brazil, Panama, Venezuela, Argentina, Bolivia. A new country record from Colombia (Atl��ntico) is added., Published as part of Garc��a, Kimberly, Botero, Juan Pablo & Santos-Silva, Antonio, 2021, A new genus of Achrysonini and new records in Cerambycidae (Coleoptera, Chrysomeloidea) from Colombia, pp. 89-109 in European Journal of Taxonomy 735 on page 102, DOI: 10.5852/ejt.2021.735.1243, http://zenodo.org/record/4554780

Lissonotus corallinus Dupont, 1836 Material examined COLOMBIA ��� 1 spec.; Atl��ntico, Usiacur��, Reserva Campesina La Monta��a; 10��46���2.6��� N, 75��0.2���34��� W; 260 m a.s.l.; 12 May 2018; K. Garc��a leg; tropical dry forest, manual capture; UARC ��� 1 spec.; same collection data as for preceding; 14 Feb. 2018; fruit trap; UARC ��� 1 spec.; same collection data as for preceding; 17 Mar. 2018; UARC. Geographical distribution Panama, Colombia (Antioquia, Bol��var, Boyac��, Choc��, Cundinamarca, Magdalena, Santander, Tolima, Valle del Cauca), Venezuela, Brazil. New department record is added: Atl��ntico (Colombia)., Published as part of Garc��a, Kimberly, Botero, Juan Pablo & Santos-Silva, Antonio, 2021, A new genus of Achrysonini and new records in Cerambycidae (Coleoptera, Chrysomeloidea) from Colombia, pp. 89-109 in European Journal of Taxonomy 735 on page 99, DOI: 10.5852/ejt.2021.735.1243, http://zenodo.org/record/4554780

Piola colombica Martins & Galileo, 1999 Material examined COLOMBIA ��� 1 spec.; Atl��ntico, Usiacur��, Reserva Campesina La Monta��a; 10��46���2.6��� N, 75��0.2���34��� W; 260 m a.s.l.; 12���13 May 2018; K. Garc��a leg; tropical dry forest, light trap; UARC. Geographical distribution Colombia (Bol��var). New department record is added: Atl��ntico (Colombia)., Published as part of Garc��a, Kimberly, Botero, Juan Pablo & Santos-Silva, Antonio, 2021, A new genus of Achrysonini and new records in Cerambycidae (Coleoptera, Chrysomeloidea) from Colombia, pp. 89-109 in European Journal of Taxonomy 735 on page 106, DOI: 10.5852/ejt.2021.735.1243, http://zenodo.org/record/4554780, {"references":["Martins U. R. & Galileo M. H. M. 1999. Tribo Hesperophanini. In: Martins U. R. (ed.) Cerambycidae Sul- Americanos (Coleoptera) Taxonomia Vol. 3: 1 - 117. Sociedade Brasileira de Entomologia, S \" o Paulo."]}

Ysachron pilosus gen. et sp. nov. urn:lsid:zoobank.org:act: 22FB104A-E069-4F84-9214-C5AD9ACA1877 Figs 1–13, 17–29 Differential diagnosis As for genus. Etymology The species epithet comes from the Latin ‘ pilosus ’, referring to the general appearance of the species, covered by long and erect setae. Material examined Holotype COLOMBIA • 1 ♂; Bolívar, San Jacinto, Reserva La Flecha; 09°51′12.4″ N, 75°10′41.4″ W; 324 m a.s.l.; 19 Feb. 2018; K. García leg; tropical dry forest, beating sheet; MPUJ _ ENT 0071150. Paratypes COLOMBIA • 1 ♂; Atlántico, Usiacurí, Reserva Campesina La Montaña; 10°46′2.6″ N 75°0.2′34″ W; 260 m a.s.l.; 15–16 Feb. 2018; K. García leg; tropical dry forest, white light trap; MZSP • 1 ♂; same collection data as for preceding; 17–18 Mar. 2018; MPUJ_ENT 0071151 • 1 ♀; same collection data as for holotype; MZSP • 1 ♀; same collection data as for preceding; 16–17 Mar. 2018; UV light trap; MPUJ_ENT 0071152. Description of holotype male (Figs 1–4, 10, 13, 17–29) COLORATION. Integument brown with yellowish-white setae, whiter depending on light intensity. Head and prothorax reddish brown. Antennae light brown; scape and pedicel slightly darker; antennomeres III – VI with apical margin dark brown. Ventral surface reddish brown, metaventrite darker on some areas. Base of femora light brown, remaining surface dark brown. Apical margin of tibiae dark. Body covered by long and erect, dense yellowish-white setae. HEAD. Frons alveolate. Area between antennal tubercles densely, coarsely alveolate. Antennal tubercles elevated, smooth. Median groove distinct from frons to area between anterior margin of upper eye lobes. Area between upper eye lobes alveolate, alveoli coarser toward antennal tubercles, smooth on central area; with abundant, long, erect setae, denser centrally. Area behind upper eye lobes slightly alveolate, with central area sparsely punctate; with a few erect setae. Genae smooth; with a few long, erect setae. Distance between upper eye lobes about three times width of an upper eye lobe. Antennae 2.1 times elytral length, reaching elytral apex at antennomere IX. Scape with sparse piliferous punctures. Antennomeres with abundant, distinctly long, erect setae, shorter toward distal segments. Antennal formula (ratio) based on length of antennomere III: scape = 0.59; pedicel = 0.14; IV = 0.76; V = 0.78; VI = 0.81; VII = 0.89; VIII = 0.81; IX = 0.76; X = 0.70; XI = 0.62; XII= 0.57. THORAX. Prothorax as long as wide. Surface of pronotum coarsely alveolate, except for small longitudinal area behind middle. Lateral sides of prothorax sparsely punctate. Prosternum slightly and transversely striated, smooth on anterior area. Prosternal process narrow, distinctly narrowed toward apex; width at narrowest point about 0.12 times width of procoxal cavity. Mesanepisternum and mesepimeron densely setose. Mesoventrite sparsely punctate. Mesoventral process microsculptured, with a few long, erect setae; emarginated at apex; width at narrowest point about 0.4 times width of mesocoxal cavity. Metanepisternum abundantly setose. Metaventrite smooth centrally, rugose on anterior sides; with sparse long, erect setae, gradually sparser toward glabrous central area. Scutellum smooth, with short, decumbent setae; posterior margin rounded. Elytra with distinct piliferous punctures, with erect setae irregularly organized. Apex of elytra obliquely truncate. LEGS. Profemora fusiform, meso- and metafemora subclavate; lateral sides of femora rugose, remaining surface smooth; setae denser toward apex. Metatarsomere I about as long as II–III together. ABDOMEN. Ventrites sparsely, finely punctate, punctures denser centrally; with long decumbent setae, erect laterally. Apex of ventrite V truncate. TERMINALIA. Tergite VIII (Fig. 17) with distal margin distinctly emarginated, with long and short yellow setae, abundant and longer laterally. Sternite VIII (Fig. 18) transverse, distal margin slightly emarginated, projected forward laterally, with long yellow setae laterally; apophysis short, rounded at apex, about as long as central area of sternite. Dorsal arc sinuous (Fig. 19). Ventral arc (Fig. 20) fork-shaped, with apophysis as long as arms; arms straight. Tegmen (Figs 24–26) about 0.8 times length of median lobe; distal region divided into parameres; parameres triangularshaped, apex rounded and covered by short setae; ring piece subrounded, proximal part truncate, without projection. Median lobe (Figs 27–29) slightly curved in lateral view; dorsal lobe with apex rounded and reaching rounded apex of ventral lobe; basal apophysis about 2.3 times length of apical region. Female (Figs 5–9, 11–12) Antennae shorter, reaching elytral apex at antennomere XII, with scape elongate; prothorax wider, with small gibbosity medially (in one female more evident – Fig. 12); surface of lateral sides of prothorax densely alveolate; ventrite V longer than precedent, with rounded apex. Measurements (in mm) Holotype male, total length: 7.5, prothorax length: 1.5, anterior prothoracic width: 1.1, posterior prothoracic width: 1.1, largest prothoracic width: 1.5, elytral length: 5.1, humeral width: 1.7. Paratypes, ♂ / ♀, n = 2 / 2. Total length: 7–8.5 / 8.8–9.1, prothorax length: 1.4–1.8 / 1.6–1.6, largest prothoracic width: 1.35–1.7 / 1.4–2, elytral length: 4.6–5.7 / 6.2–6.5, humeral width: 1.6–1.9 / 2.1–2.2.

Colobothea fasciatipennis Linsley, 1935 Material examined COLOMBIA ��� 1 spec.; Atl��ntico, Usiacur��, Reserva Campesina La Monta��a; 10��46���2.6��� N, 75��0.2���34��� W; 260 m a.s.l.; 18 Mar. 2018; K. Garc��a leg; tropical dry forest, light trap; UARC ��� 1 spec.; same collection data as for preceding; 9 Apr. 2018; manual capture; UARC. Geographical distribution Honduras, Panama, Colombia (Bol��var, Choc��, Santander). New department record is added: Atl��ntico (Colombia)., Published as part of Garc��a, Kimberly, Botero, Juan Pablo & Santos-Silva, Antonio, 2021, A new genus of Achrysonini and new records in Cerambycidae (Coleoptera, Chrysomeloidea) from Colombia, pp. 89-109 in European Journal of Taxonomy 735 on page 104, DOI: 10.5852/ejt.2021.735.1243, http://zenodo.org/record/4554780

Malacopterus tenellus (Fabricius, 1801) Material examined COLOMBIA ��� 1 spec.; Atl��ntico, Usiacur��, Reserva Campesina La Monta��a; 10��46���2.6��� N, 75��0.2���34��� W; 260 m a.s.l.; 12���14 May 2018; K. Garc��a leg; tropical dry forest, light trap; UARC. Geographical distribution United States of America (Texas, California), Mexico (Durango, Sonora, Tamaulipas), Guatemala, Belize, Nicaragua, Panama, Colombia (Antioquia, Choc��, Cundinamarca, Meta, Santander, Tolima, Valle del Cauca), Brazil (Amazonas, Par��, Mato Grosso, Maranh���o), Venezuela, Ecuador, Guyana, French Guiana, Surinam, Peru, Bolivia (La Paz, Santa Cruz), Jamaica, Cuba, Guadeloupe, Hispaniola, Honduras, Costa Rica, Dominican Republic. New department record is added: Atl��ntico (Colombia)., Published as part of Garc��a, Kimberly, Botero, Juan Pablo & Santos-Silva, Antonio, 2021, A new genus of Achrysonini and new records in Cerambycidae (Coleoptera, Chrysomeloidea) from Colombia, pp. 89-109 in European Journal of Taxonomy 735 on page 99, DOI: 10.5852/ejt.2021.735.1243, http://zenodo.org/record/4554780

Coleoxestia atrata (Gounelle, 1909) Material examined COLOMBIA ��� 1 spec.; Bol��var, San Jacinto, Reserva La Flecha; 09��51���12.4��� N, 75��10���41.4��� W; 324 m a.s.l.; 13���16 Apr. 2018; K. Garc��a leg; tropical dry forest, light trap; UARC ��� 1 spec.; same collection data as for preceding; beating sheet. UARC. Geographical distribution Colombia (Amazonas), Brazil (Tocantins, Goi��s, Paran��), Bolivia (Santa Cruz). New department record is added: Bol��var (Colombia)., Published as part of Garc��a, Kimberly, Botero, Juan Pablo & Santos-Silva, Antonio, 2021, A new genus of Achrysonini and new records in Cerambycidae (Coleoptera, Chrysomeloidea) from Colombia, pp. 89-109 in European Journal of Taxonomy 735 on page 97, DOI: 10.5852/ejt.2021.735.1243, http://zenodo.org/record/4554780

Estoloides venezuelensis Breuning, 1942 Material examined COLOMBIA ��� 1 spec.; Atl��ntico, Usiacur��, Reserva Campesina La Monta��a; 10��46���2.6��� N, 75��0.2���34��� W; 260 m a.s.l.; 15 Feb. 2018; K. Garc��a leg; tropical dry forest, UV light trap; UARC ��� 1 spec.; Bol��var, San Jacinto, Reserva La Flecha; 09��51���12.4��� N, 75��10���41.4��� W; 324 m a.s.l.; 16 Mar. 2018; K. Garc��a leg; tropical dry forest, manual capture; UARC. Geographical distribution Venezuela. A new country record from Colombia (Atl��ntico and Bol��var) is added., Published as part of Garc��a, Kimberly, Botero, Juan Pablo & Santos-Silva, Antonio, 2021, A new genus of Achrysonini and new records in Cerambycidae (Coleoptera, Chrysomeloidea) from Colombia, pp. 89-109 in European Journal of Taxonomy 735 on page 104, DOI: 10.5852/ejt.2021.735.1243, http://zenodo.org/record/4554780

Cacostola colombiana Martins & Galileo, 1999 Material examined COLOMBIA • 1 spec.; Atlántico, Usiacurí, Reserva Campesina La Montaña; 10°46′2.6″ N, 75°0.2′34″ W; 260 m a.s.l.; 12–13 May 2018; K. García leg; tropical dry forest, beating sheet, light trap; UARC • 1 spec.; same collection data as for preceding; 10 Jun. 2018; UARC. Geographical distribution Colombia (Bolívar). New department record is added: Atlántico (Colombia).

Ysachron gen. nov. urn:lsid:zoobank.org:act: B31E5244-31DC-49D7-8838-93850EEA9581 Figs 1–12 Type species Ysachron pilosus gen. et sp. nov., here designated. Differential diagnosis Ysachron gen. nov. is similar to some genera of Hesperophanini Mulsant, 1839, Oemini and Achrysonini. Despite not having the setae between ommatidia, we allocate it in Achrysonini due to the presence of the following characteristics: eyes coarsely faceted; antennomeres unarmed; antennae in males longer than body; scape shorter than antennomere III; procoxal cavities open and not strongly angulate laterally (Fig. 13, Ysachron pilosus gen. et sp. nov.; Fig. 14, Achryson surinamum (Linnaeus, 1767)); prosternal process without lateral projections apically; and metatibiae not carinate. The presence or absence of setae between ommatidia is a characteristic that also varies among subtribes of Oemini (Martins, 1997): present in Oemina Lacordaire, 1868, absent in Methioidina Martins, 1997 (except in Proeme Martins, 1978). Although we are aware of the great similarity between the tribes Achrysonini, Hesperophanini and Oemini, Ysachron gen. nov. differs from Hesperophanini and Oemini by having procoxal cavities not strongly angulate laterally (Figs 13–14), while they are strongly angulate in the latter two (Figs 15–16). The new genus also differs from genera of Hesperophanini by the median lobe with the apical region shorter than basal apophysis (Figs 27–29). Among the genera of Achrysonini, Ysachron gen. nov. is similar to Achryson by the rounded prothorax sides without projections, basal antennomeres linear, scape as long as half of the length of antennomere III, and fuscous aspect. It differs as follows: eyes lacking setae between the ommatidia; surface of the pronotum alveolate; antennae 12-segmented; elytra with long setae; and meso- and metafemora subclavate.Species of Achryson have setae between ommatidia, surface of the pronotum microsculptured, antennae 11-segmented, elytra with short setae, and femora fusiform. Also, unlike some other genera in Achrysonini, Ysachron gen. nov. does not show sexual punctation differences. Etymology The name Ysachron is an anagram of Achryson, a similar genus of Achrysonini. The gender is masculine. Description Head narrowed behind eyes, densely alveolate between upper eye lobes. Median groove well-marked between antennal tubercles. Antennal tubercles weakly elevated, with obtuse apex. Eyes coarsely faceted, not coplanar with surface around them; without setae between ommatidia; upper eye lobes distant from each other; lower eye lobes large, about three times the length of genae. Genae small, with rounded apex. Labrum small, when together with clypeus, longer than frons. Mandibles short, with acute apex. Maxillary and labial palpi of similar length. Antennae 12-segmented, longer than body in males, as long as body in females; scape short, somewhat cylindrical, as long as about half length of antennomere III; antennomere III longer than IV. Prothorax subcylindrical; lateral margin rounded and unarmed, constricted in anterior and posterior margins. Prosternal process narrow, parallel sided, with apex curved inwards. Mesoventrite tumid. Mesoventral process emarginated at apex. Metaventrite rectangular, slightly wider than long, parallel-sided. Scutellum small. Elytra not exposing abdomen, parallel-sided; humeri rounded; base wider than posterior margin of prothorax; surface not carinate. Femora from subfusiform to slightly clavate. Tibiae slightly widened toward apex. Abdominal ventrite I the largest (including abdominal process), ventrites II–V subequal in length. Key to South American genera of Achrysonini (modified and translated from Martins 2002 and Monné & Monné 2004) 1. Setae between ommatidia absent; antennae 12-segmented................................. Ysachron gen. nov. – Setae between ommatidia present; antennae 11-segmented............................................................. 2 2. Sides of prothorax with long spine (longer than pedicel), with curved apex backward..................................................................................................................... Drascalia Fairmaire & Germain, 1864 – Sides of prothorax unarmed (without spines or with small gibbosity) or at most with short triangular tubercle............................................................................................................................................. 3 3. Pronotum with two tubercles on anterior third; elytra with longitudinal elevation, more evident near base, reaching apical fourth, delimiting a flattened area near suture.. Abyarachryson Martins, 2002 – Pronotum without tubercles (except for small gibbosities in some species of Achryson); elytra uniformly convex or flattened on apical ¾....................................................................................... 4 4. Elytra flattened on apical ¾; metafemora linear..................... Neoachryson Monné & Monné, 2004 – Elytra uniformly convex, metafemora not linear.............................................................................. 5 5. Metafemora strongly clavate............................................................................................................ 6 – Metafemora subfusiform, with elongate club................................................................................... 7 6. Antennomere III longer than scape and other antennomeres...................... Huequenia Cerda, 1890 – Antennomere III shorter than scape and other antennomeres.............. Esseiachryson Martins, 2002 7. Elytra with contrasting punctures and glabrous perimeter................... Cotyachryson Martins, 2002 – Elytra without contrasting punctures................................................................................................ 8 8. Basal antennomeres thickened; sides of prothorax with small central gibbosity......................................................................................................................................................... Cerdaia Monné, 2006 – Basal antennomeres linear; sides of prothorax rounded................................................................... 9 9. Scape about as long or slightly shorter than antennomere III; elytra with long setae and shining aspect...................................................................................................... Xenocompsa Martins, 1965 – Scape about as long as half the length of antennomere III; elytra often with short setae and general aspect not shining.......................................................................... Achryson Audinet-Serville, 1833

Criodion cinereum (Olivier, 1795) Material examined COLOMBIA ��� 1 spec.; Bol��var, San Jacinto, Reserva La Flecha; 09��51���12.4��� N, 75��10���41.4��� W; 324 m a.s.l.; 13���16 Apr. 2018; K. Garc��a leg; tropical dry forest, light trap; UARC. Geographical distribution Costa Rica, Panama, Colombia (Amazonas), Venezuela, Surinam, French Guiana, Guyana, Peru, Brazil (Amazonas), Bolivia (Santa Cruz), Puerto Rico (?), Paraguay (?). New department record is added: Bol��var (Colombia)., Published as part of Garc��a, Kimberly, Botero, Juan Pablo & Santos-Silva, Antonio, 2021, A new genus of Achrysonini and new records in Cerambycidae (Coleoptera, Chrysomeloidea) from Colombia, pp. 89-109 in European Journal of Taxonomy 735 on page 97, DOI: 10.5852/ejt.2021.735.1243, http://zenodo.org/record/4554780

Coleoxestia rubromaculata (Gounelle, 1909) Material examined COLOMBIA ��� 1 spec.; Bol��var, San Jacinto, Reserva La Flecha; 09��51���12.4��� N, 75��10���41.4��� W; 324 m a.s.l.; 13���16 Apr. 2018; K. Garc��a leg; tropical dry forest, light trap; UARC. Geographical distribution Nicaragua, Honduras, Costa Rica, Panama, Colombia, Ecuador, French Guiana, Peru, Brazil (Rond��nia, Mato Grosso, Goi��s, Distrito Federal). The species is registered from Colombia but without any further locality. Herein, the species is registered from the department of Bol��var (Colombia)., Published as part of Garc��a, Kimberly, Botero, Juan Pablo & Santos-Silva, Antonio, 2021, A new genus of Achrysonini and new records in Cerambycidae (Coleoptera, Chrysomeloidea) from Colombia, pp. 89-109 in European Journal of Taxonomy 735 on page 97, DOI: 10.5852/ejt.2021.735.1243, http://zenodo.org/record/4554780

Bebelis picta Pascoe, 1875 Material examined COLOMBIA ��� 1 spec.; Atl��ntico, Usiacur��, Reserva Campesina La Monta��a; 10��46���2.6��� N, 75��0.2���34��� W; 260 m a.s.l.; 12 May 2018; K. Garc��a leg; tropical dry forest, light trap; UARC. Geographical distribution Mexico (Veracruz, Chiapas, Guerrero), Guatemala, Nicaragua, Honduras, Cuba, Costa Rica, Panama, Venezuela, Colombia, French Guiana, Brazil (Maranh���o, Goi��s, Cear��, Bahia, Minas Gerais, Esp��rito Santo, Rio de Janeiro, S���o Paulo, Paran��, Rio Grande do Sul), Bolivia (Santa Cruz), Paraguay, Argentina (Buenos Aires), Martinique, St. Vincent. New department record is added: Atl��ntico (Colombia)., Published as part of Garc��a, Kimberly, Botero, Juan Pablo & Santos-Silva, Antonio, 2021, A new genus of Achrysonini and new records in Cerambycidae (Coleoptera, Chrysomeloidea) from Colombia, pp. 89-109 in European Journal of Taxonomy 735 on page 103, DOI: 10.5852/ejt.2021.735.1243, http://zenodo.org/record/4554780

Adesmus divus (Chabrillac, 1857) Material examined COLOMBIA ��� 1 spec.; Atl��ntico, Usiacur��, Reserva Campesina La Monta��a; 10��46���2.6��� N, 75��0.2���34��� W; 260 m a.s.l.; 14 May 2018; K. Garc��a leg; tropical dry forest, manual capture; UARC. Geographical distribution Colombia (Guajira), Brazil (Mato Grosso, Goi��s, Distrito Federal, Maranh���o, Minas Gerais, Esp��rito Santo Rio de Janeiro, S���o 649 Paulo, Paran��, Rio Grande do Sul), French Guiana, Bolivia (Santa Cruz), Paraguay, Argentina (Misiones). New department record is added: Atl��ntico (Colombia)., Published as part of Garc��a, Kimberly, Botero, Juan Pablo & Santos-Silva, Antonio, 2021, A new genus of Achrysonini and new records in Cerambycidae (Coleoptera, Chrysomeloidea) from Colombia, pp. 89-109 in European Journal of Taxonomy 735 on page 105, DOI: 10.5852/ejt.2021.735.1243, http://zenodo.org/record/4554780

Deliathis quadritaeniata (White, 1846) Material examined COLOMBIA ��� 1 spec.; Bol��var, San Jacinto, Reserva La Flecha; 09��51���12.4��� N, 75��10���41.4��� W; 324 m a.s.l.; 16 Apr. 2018; K. Garc��a leg; tropical dry forest, UV light trap; UARC. Geographical distribution Costa Rica, Panama, Colombia Venezuela, Ecuador. The species is registered from Colombia but without any specific locality. Herein, the species is registered from the department of Bol��var (Colombia)., Published as part of Garc��a, Kimberly, Botero, Juan Pablo & Santos-Silva, Antonio, 2021, A new genus of Achrysonini and new records in Cerambycidae (Coleoptera, Chrysomeloidea) from Colombia, pp. 89-109 in European Journal of Taxonomy 735 on page 105, DOI: 10.5852/ejt.2021.735.1243, http://zenodo.org/record/4554780

Hippopsis ocularis Galileo & Martins, 1995 Material examined COLOMBIA ��� 1 spec.; Atl��ntico, Usiacur��, Reserva Campesina La Monta��a; 10��46���2.6��� N, 75��0.2���34��� W; 260 m a.s.l.; 10 Jun. 2018; K. Garc��a leg; tropical dry forest, beating sheet; UARC. Geographical distribution Bolivia (Cochabamba, Santa Cruz); French Guiana. A new country record from Colombia (Atl��ntico) is added., Published as part of Garc��a, Kimberly, Botero, Juan Pablo & Santos-Silva, Antonio, 2021, A new genus of Achrysonini and new records in Cerambycidae (Coleoptera, Chrysomeloidea) from Colombia, pp. 89-109 in European Journal of Taxonomy 735 on page 102, DOI: 10.5852/ejt.2021.735.1243, http://zenodo.org/record/4554780

Physopleurus erikae Santos-Silva & Martins, 2009 Material examined COLOMBIA • 1 spec.; Bolívar, San Jacinto, Reserva La Flecha; 09°51′12.4″ N, 75°10′41.4″ W; 324 m a.s.l.; 13 Apr. 2018; K. García leg; tropical dry forest, light trap; UARC. Geographical distribution Colombia (Valle del Cauca). New department record is added: Bolívar (Colombia).

Tulcus fulvofasciatus (Dillon & Dillon, 1945) Material examined COLOMBIA ��� 1 spec.; Atl��ntico, Usiacur��, Reserva Campesina La Monta��a; 10��46���2.6��� N, 75��0.2���34��� W; 260 m a.s.l.; 12���14 May 2018; K. Garc��a leg; tropical dry forest, light trap; UARC. Geographical distribution Costa Rica, Panama, Colombia. The species is registered from Colombia but without any specific locality. Herein, the species is registered from the department of Atl��ntico (Colombia)., Published as part of Garc��a, Kimberly, Botero, Juan Pablo & Santos-Silva, Antonio, 2021, A new genus of Achrysonini and new records in Cerambycidae (Coleoptera, Chrysomeloidea) from Colombia, pp. 89-109 in European Journal of Taxonomy 735 on page 106, DOI: 10.5852/ejt.2021.735.1243, http://zenodo.org/record/4554780

Ischionodonta colombiana Napp & Marques, 1999 Material examined COLOMBIA • 1 spec.; Bolívar, San Jacinto, Reserva La Flecha; 09°51′12.4″ N, 75°10′41.4″ W; 324 m a.s.l.; 13–16 Apr. 2018; K. García leg; tropical dry forest, UV light trap; UARC. Geographical distribution Colombia (Magdalena). New department record is added: Bolívar (Colombia).

Stizocera geniculata (Pascoe, 1866) Geographical distribution: Trinidad; Colombia (Atlántico, Magdalena), new department record (Atlántico); Venezuela; Brazil (Roraima, Rondônia). Specimens examined: Colombia, Atlántico: Usiacurí; (Reserva Campesina La Montaña, 10°46.0′02.6″N, 75°00.2′34.0″W, tropical dry forest), 12.V.2018, K. García col., UV light trap (1♂, 1♀ UARC)., Published as part of García, Kimberly & Nascimento, Francisco Eriberto de Lima, 2020, Elaphidiini (Coleoptera, Cerambycidae) from the Caribbean region of Colombia: New species, taxonomic notes and new geographical records, pp. 1-8 in Papéis Avulsos de Zoologia (Pap. Avulsos Zool., S. Paulo) (Pap. Avulsos Zool., S. Paulo) 60 (23) on page 7, DOI: 10.11606/1807-0205/2020.60.special-issue.23, http://zenodo.org/record/4615223

Stizocera poeyi (Chevrolat, 1838) Geographical distribution: Cuba; Costa Rica; Panama; Colombia (Bolívar, Tolima), new department record (Bolívar); Venezuela; French Guiana; Brazil (Acre, Amazonas, Rondônia); Bolivia (Santa Cruz). Specimens examined: Colombia, Bolívar: San Jacinto (Reserva La Flecha, 09°51′12.4″N, 75°10′41.4″W, tropical dry forest), 23-16.IV.2017, K. García col., white light trap (1♀ UARC), manual capture (1♀ UARC)., Published as part of García, Kimberly & Nascimento, Francisco Eriberto de Lima, 2020, Elaphidiini (Coleoptera, Cerambycidae) from the Caribbean region of Colombia: New species, taxonomic notes and new geographical records, pp. 1-8 in Papéis Avulsos de Zoologia (Pap. Avulsos Zool., S. Paulo) (Pap. Avulsos Zool., S. Paulo) 60 (23) on page 8, DOI: 10.11606/1807-0205/2020.60.special-issue.23, http://zenodo.org/record/4615223

Amethysphaerion falsus Martins, 1995 Geographical distribution: Venezuela; Colombia (Atlántico), new country record. Specimens examined: Colombia, Atlántico: Usiacurí; (Reserva Campesina La Montaña, 10°46.0′02.6″N, 75°00.2′34.0″W, tropical dry forest), 12.V.2018, K. García col., white light trap (2♀ UARC)., Published as part of García, Kimberly & Nascimento, Francisco Eriberto de Lima, 2020, Elaphidiini (Coleoptera, Cerambycidae) from the Caribbean region of Colombia: New species, taxonomic notes and new geographical records, pp. 1-8 in Papéis Avulsos de Zoologia (Pap. Avulsos Zool., S. Paulo) (Pap. Avulsos Zool., S. Paulo) 60 (23) on page 6, DOI: 10.11606/1807-0205/2020.60.special-issue.23, http://zenodo.org/record/4615223

Stizocera rugicollis (Guérin-Méneville, 1844) Geographical distribution: Nicaragua; Costa Rica; Panama; Colombia (Atlántico), new department record (Atlántico). Specimens examined: Colombia, Atlántico: Usiacurí; (Reserva Campesina La Montaña, 10°46.0′02.6″N, 75°00.2′34.0″W, tropical dry forest), 14.V.2018, K. García col., manual capture (1♂, 1♀ UARC), UV light trap (1♀ UARC)., Published as part of García, Kimberly & Nascimento, Francisco Eriberto de Lima, 2020, Elaphidiini (Coleoptera, Cerambycidae) from the Caribbean region of Colombia: New species, taxonomic notes and new geographical records, pp. 1-8 in Papéis Avulsos de Zoologia (Pap. Avulsos Zool., S. Paulo) (Pap. Avulsos Zool., S. Paulo) 60 (23) on page 8, DOI: 10.11606/1807-0205/2020.60.special-issue.23, http://zenodo.org/record/4615223

Enaphalodes boyacanus Martins, 2005 Geographical distribution: Costa Rica; Panama; Colombia (Bolívar, Boyacá), new department record (Bolívar). Specimens examined: Colombia, Bolívar: San Jacinto (Reserva La Flecha, 324 m, 09°51′12.4″N, 75°10′41.4″W, tropical dry forest), 15.III.2018, García, K. col., fruit-bated trap (1♂ UARC)., Published as part of García, Kimberly & Nascimento, Francisco Eriberto de Lima, 2020, Elaphidiini (Coleoptera, Cerambycidae) from the Caribbean region of Colombia: New species, taxonomic notes and new geographical records, pp. 1-8 in Papéis Avulsos de Zoologia (Pap. Avulsos Zool., S. Paulo) (Pap. Avulsos Zool., S. Paulo) 60 (23) on page 7, DOI: 10.11606/1807-0205/2020.60.special-issue.23, http://zenodo.org/record/4615223, {"references":["Martins, U. R. 2005. Tribo Elaphidionini. In: Martins, U. R. (Org.). Cerambycidae Sul-Americanos (Coleoptera). Taxonomia. Curitiba, Sociedade Brasileira de Entomologia. v. 7, 393 p."]}

Mephritus apicatus (Linsley, 1935) (Figs. 14-15) Geographical distribution: Mexico (Chiapas, Oaxaca); Nicaragua; Costa Rica; Panama; Brazil (Rondônia); Colombia (Atlántico, Bolívar), new country record. Material examined: Colombia, Atlántico: Usiacurí (Reserva Campesina La Montaña, 260 m, 10°46.0′02.6″N, 75°00.2′34.0″W, tropical dry forest), 14.V.2018, García, K. col., UV light trap (1♀ UARC); Bolívar: San Jacinto (Reserva La Flecha, 324 m, 09°51′12.4″N, 75°10′41.4″W, tropical dry forest), 15-16.IV.2018, García, K. col., UV light trap (3♀ UARC), white light trap (1♂, 1♀ MZSP). Remarks: This species was described by Linsley (1935) provisionally in the genus Nephalius Blanchard, 1843, and later transferred to Mephritus by Napp & Martins, 1982. Originally, Linsley (1935) described the species habitus as yellowish-testaceous, with the head (in front of the eyes), antennae, legs, and apices of elytra black or rufo-piceous; he also mentioned that the elytral apex is spinose but did not specify any variation regarding the length of the spine. Specimens of M. apicatus from Colombia were examined and compared with specimens from the MZSP, and a chromatic variation was noticed. The head was completely dark in some specimens (not only in front of the eyes) (Fig. 14), while others were reddish, only dark in front of the eyes (Fig. 15); the color of the legs is also variable, with a tendency to be dark toward the femoral apex. Moreover, the length of the elytral spines is also variable among specimens., Published as part of García, Kimberly & Nascimento, Francisco Eriberto de Lima, 2020, Elaphidiini (Coleoptera, Cerambycidae) from the Caribbean region of Colombia: New species, taxonomic notes and new geographical records, pp. 1-8 in Papéis Avulsos de Zoologia (Pap. Avulsos Zool., S. Paulo) (Pap. Avulsos Zool., S. Paulo) 60 (23) on page 7, DOI: 10.11606/1807-0205/2020.60.special-issue.23, http://zenodo.org/record/4615223, {"references":["Linsley, G. 1935. Notes and descriptions of new or little known neotropical Sphaerionini (Coleoptera, Cerambycidae). Revista de Entomologia, 5 (2): 139 - 149.","Napp, D. S. & Martins, U. R. 1982. Mephritus Pascoe, 1 866 (Coleoptera, Cerambycidae): revalidacao do genero, chave para especies, notas sinonimicas e descricoes. Revista Brasileira Entomologia, 26 (1): 71 - 86."]}