identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
0EC620A4000651DFB42F44C5AB49CF62.text	0EC620A4000651DFB42F44C5AB49CF62.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Lamprosoma cambuci Santos, Jorge & Zarbin 2026	<div><p>5.3. 2. Lamprosoma cambuci Santos, Jorge &amp; Zarbin sp. nov.</p><p>Figures 2, 3, 4, 5, 6, 12</p><p>Diagnoses.</p><p>The species has an oval body in dorsal view, strongly convex dorsally and flat ventrally (Fig. 2 A, B). The head, pronotum, and elytra are matte, iridescent blue (Fig. 2 A – H), while the mouthparts, antennae, legs, and abdomen are bluish black. The prosternal process is longer than wide and gently constricted in the middle in females. The last abdominal ventrite is larger than the previous three; in females, it presents a concavity densely punctate and covered with setae, while in males, it bears a concentrated tuft of setae medially at the apex. The apical margin of the dorsal genital valve uniformly slender (Fig. 6 D), bearing short and thick setae. Dorsal valve medially projected. Dorsal sclerites paired, elongated, curved to follow the contour of the ventral wall. Ventral sclerites paired, elongated, reaching the median portion of the aedeagus, apically sinuous. Sclerite in the basal region possibly homologous to the ejaculatory hook (Fig. 6 A – C). Single spermatheca, without chamber formation (Fig. 6 E). A large chitinous cushion (chitinpolster) present, with lateral folds widened, bending upwards and posteriorly extended into a longitudinal twig, median fusion of the lateral folds of the chitinpolster, forming an H-like structure. Styli present and fused. Spermathecal ducts intricate.</p><p>Description.</p><p>MALE: Body. Oval, strongly convex dorsally and flat ventrally (Fig. 2 A, B). — Integument color. Head, pronotum, and elytra lead blue (Fig. 2 A, B), with violaceous reflections; ventral surface, including legs and abdomen, dark blue. Elytra with ten rows of punctures extending from the base to the apex, where they merge. In dorsal view, only eight rows are visible. Each puncture with a short, yellowish hair. — Head. Frons with fine punctures, evenly distributed (Figs 4, 5 A – E). Head anteriorly flat, with very slight, rounded impression in the interocular space in the males (Fig. 2 C). Eyes emarginated at the level of antenna insertion. Antennae (Figs 2 B, 4 F) short, with eleven segments, inserted between the base of the eye and lateral edges of the clypeus. Labrum short, sub quadrangular, with angulate lateral margins. — Prothorax. Pronotum convex, narrower than the base of elytra, sinuous at base, with fine punctures like those on frons in the posterior region and coarser in the anterior region; prosternal process longer than wide (Figs 2 B, 4 E – G), sinuous medially, and truncated at apex. — Meso- and metathorax. Mesothorax small, with triangular scutellum, with acute apex (Fig. 2 A). Epipleura narrow. Elytral apex with the inner surface bearing a depression that receives the denticles on the apex of the last ventrite, forming an elytral locking mechanism. Prosternal process narrow and length than width. Anterior legs (Fig. 2 B, D) with femora with the inner margin project into the median portion, tibiae with a small tooth-like in the internal and external portion apex. Four visible tarsomeres; the last tarsomere protrudes less than one-third of the anterior tarsal lobe, with an appendiculate claw (Fig. 4 I). Middle and Posterior legs (Figs 2 B, 4 G) similar to the anterior leg, except for the transverse coxae and femora lack internal projections. — Abdomen. with five ventrites, the last serrated at the apex (elytral lock mechanism) (Fig. 4 H). Ventrite I with lateral arc-shaped depressions to receive the metafemora (Figs 2 B, 4 G); Ventrite II to IV medially punctate and with short setae, ventrite V more densely punctate and with long setae. — Aedeagus (Fig. 6 A – D). Apical margin of the dorsal valve uniformly slender, bearing short and thick setae. Dorsal valve medially projected. Apical sclerites paired, elongate, curved to follow the contour of the ventral wall. Median sclerites paired, elongate, reaching the median portion of the aedeagus, apically sinuous. Sclerite in the basal region possibly homologous to the ejaculatory hook. — FEMALE (Figs 3 A – D, 5 A – F, 6 E): Head anteriorly flat, with a very strongly, roundly impressed on the interocular space (Figs 3 C, 5 C, 5 E). Prosternal process length than width (Figs 3 B, 5 E). Abdominal ventrite V more strongly punctate and densely pilose than in males. One single spermatheca (Fig. 6 E), without chamber formation, hook-shaped. A large chitinous cushion (chitinpolster) present, with lateral folds widened, bending upwards and posteriorly extended into a longitudinal twig, median fusion of lateral folds of the chitinpolster, forming an H-like structure. Styli present and fusion. Spermathecal ducts intricate.</p><p>Egg case.</p><p>Brownish, host plant’s wood fibers visible, with three vertical rows of externally projecting spicules surrounding the entire case, forming a total of seven vertical lines of spicules (Fig. 12 J, L, K).</p><p>Larval case.</p><p>Brownish, “ bonnet Phrygian ” - like; host plant’s wood fibers visible (Fig. 12 C, E, F).</p><p>Host plants.</p><p>Campomanesia phaea (O. Berg) Landrum ( Myrtaceae).</p><p>Parasitoid.</p><p>Undetermined wasp species belonging to Brasema Cameron, 1884 ( Hymenoptera: Chalcidoidea: Eupelmidae) (Fig. 14 A – F).</p><p>Geographical distribution.</p><p>Brazil: Minas Gerais, Aiuruoca (Fig. 11).</p><p>Type series.</p><p>The type series of the new species of Lamprosoma comprises 13 specimens: the holotype (male) and five paratypes (♀ and ♂), being the holotype and three paratypes deposited in the DZUP, along with the parasitoid wasp (a single individual that emerged from a pupal case), while two paratypes (one ♀ and one ♂) were deposited in the Invertebrate Collection of the Instituto Nacional de Pesquisas da Amazônia – INPA. Seven paratypes (♀ and ♂) that were used in the molecular extraction and in the scanning electron microscope (SEM) images were also deposited in the DZUP and INPA. — DZUP. Holotype ♂ labeled: BRASIL: Minas Gerais, Aiuruoca, | Sítio Angai Cambuci . | 28. VIII. 2024 | Col. Thiago Nicoliello, 2024; Consumindo Campomanesia phaea | (O. Berg) Landrum | Nome popular: Cambuci.; HOLOTYPE | Lamprosoma cambuci | Santos, Jorge &amp; Zarbin, 2025; DZUP | 325202 . — One paratype ♀ and two paratypes ♂ labeled: BRASIL: Minas Gerais, Aiuruoca, | Sítio Angai Cambuci . | 28. VIII. 2024 | Col. Thiago Nicoliello, 2024; Consumindo Campomanesia phaea | (O. Berg) Landrum | Nome popular: Cambuci.; PARATYPE | Lamprosoma cambuci | Santos, Jorge &amp; Zarbin, 2025; DZUP | 325199; 325200; 325201 . — Used in molecular and MEV analyses: Three ♀ and three ♂ labeled: BRASIL: Minas Gerais, Aiuruoca, | Sítio Angai Cambuci . | 28. VIII. 2024 | Col. Thiago Nicoliello, 2024; Consumindo Campomanesia phaea | (O. Berg) Landrum | Nome popular: Cambuci.; PARATYPE | Lamprosoma cambuci | Santos, Jorge &amp; Zarbin, 2025 | Det. A. T. dos Santos, 2024; DZUP | 325186; 325187; 325188; 325189; 325190; 325191; 325192; 325193 . — INPA. One paratype ♀ and one paratype ♂ labeled: BRASIL: Minas Gerais, Aiuruoca, | Sítio Angai Cambuci . | 28. VIII. 2024 | Col. Thiago Nicoliello, 2024; Consumindo Campomanesia phaea | (O. Berg) Landrum | Nome popular: Cambuci.; PARATYPE | Lamprosoma cambuci | Santos, Jorge &amp; Zarbin, 2025; INPA -COL | 002861; INPA -COL 002862 .</p><p>Etymology.</p><p>The specific name “ cambuci ” is used in apposition and was chosen based on the common name of the host plants consumed by the species. The term cambuci originates from the Tupi-Guarani Indians and means “ pot of water, ” referring to the vase-like shape of the fruit. According to Navarro (2013), the Tupi-Guarani term kamu’si denotes a vase or a funerary urn used by the Tupis.</p><p>Remarks.</p><p>This species belongs to the “ D 2 A ” group delimited by Lacordaire (1848) (see Table S 1). This species closely resembles Lamprosoma azureum in terms of its external morphology, particularly coloration. These species exhibit a uniform blue dorsal surface without additional spots. In both species, the dorsal surface is a matte and iridescent blue. The ventral sclerites are paired and elongate, extending to the median portion of the aedeagus, a trait shared by La. azureum and La. cambuci . We thus regard them as likely sister species.</p><p>Differences between the two include the following: the ventral apical margin of the ventral valve is laterally thickened in La. azureum, while in La. cambuci it is uniformly slender, with short and thick setae present in both species. In L. cambuci, these sclerites are apically sinuous, whereas in La. azureum, the sclerites follow the curvature of the ventral wall. The dorsal sclerite is found exclusively in La. cambuci . The dorsal valve is medially projected in both species. The sclerite in the basal region is possibly homologous to the ejaculatory hook, present in both species. The female has a large chitinous cushion (chitinpolster) present, with lateral folds widened, bending upwards and posteriorly extended into a longitudinal twig, resembling Lamprosoma sp. as mentioned by Schöller (2008), except for the median fusion of the lateral folds of the chitinpolster, forming an H-like structure.</p></div>	https://treatment.plazi.org/id/0EC620A4000651DFB42F44C5AB49CF62	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.		Pensoft via Plazi	Santos, Aluska Tavares;Jorge, Isaac Reis;Fianco, Marcos;Sampaio, Aline;Martins, André Luis;Rafael, José Albertino;Paladini, Andressa;Zarbin, Paulo Henrique Gorgatti	Santos, Aluska Tavares, Jorge, Isaac Reis, Fianco, Marcos, Sampaio, Aline, Martins, André Luis, Rafael, José Albertino, Paladini, Andressa, Zarbin, Paulo Henrique Gorgatti (2026): Revisiting Lamprosoma and expanding knowledge of Lychnophaes (Coleoptera: Chrysomelidae, Lamprosomatinae): Molecular phylogeny, new species, host plants, associated parasitoid wasps and geographical records. Arthropod Systematics & Phylogeny 84: 719-744, DOI: 10.3897/asp.84.e181950
CACAD84A41005012B6A525A48A8DE8AF.text	CACAD84A41005012B6A525A48A8DE8AF.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Lamprosoma Kirby 1818	<div><p>5.3. 1. Genus Lamprosoma Kirby, 1818</p><p>Kirby 1818: 445 (genus description); Lacordaire 1848: 574 (species description, distribution); Kirby and Spence 1865: 262 (larval case); Girard 1873: 775 (natural history); Chapuis 1874: 216 (catalog); Jacoby 1880: 90 (catalog); Weise 1882 (species description), Jacoby 1908 (species description); Fiebrig 1910: 236 (illustrated description of larva, host plant); Moreira 1913 (natural history); Achard 1914 (catalog); Böving and Craighead 1930: 64 (key to the larvae of the subfamily); Chen 1940 (species description); Chevrolat 1842 (catalog); Blackwelder 1946 (catalog); Monrós 1948 b: 81 (species description); Monrós 1949 (natural history, immature description); Fiori 1951: 183 (case construction); Monrós 1956: 59 (revision of tribes, distribution, figures); Monrós 1960: 9 (catalog); Ogloblin and Medvedev 1971: 41 (illustration); Linsenmaier 1972: 158 (illustrations of egg and larval cases); Kasap and Crowson 1976: 100 (citation); Erber 1988: 143 (citation); Reid 1995: 82–84 (morphological characters); Caxambú and Almeida 1999: 244 (immature description, species redescription); Caxambú 1998: 1–65 (biology); Wikler et al. 1999: 660 (biology, host plant, fecal case); Jolivet and Verma 2002: 50, 501 (host plant); Caxambú and Almeida 2003: 330 (species description, species redescription, key); DalMolin 2005: 7 (pest); Casari and Texeira 2008: 39 (illustrated descriptions of larva and pupa); Chamorro 2014: 226 (tribe description); Chaboo et al. 2016 (immature catalogue); Agrain et al. 2017 (Camptosomata of Argentina).</p><p>Type species.</p><p>Lamprosoma bicolor Kirby, 1818: 445 . By original monotypy.</p></div>	https://treatment.plazi.org/id/CACAD84A41005012B6A525A48A8DE8AF	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.		Pensoft via Plazi	Santos, Aluska Tavares;Jorge, Isaac Reis;Fianco, Marcos;Sampaio, Aline;Martins, André Luis;Rafael, José Albertino;Paladini, Andressa;Zarbin, Paulo Henrique Gorgatti	Santos, Aluska Tavares, Jorge, Isaac Reis, Fianco, Marcos, Sampaio, Aline, Martins, André Luis, Rafael, José Albertino, Paladini, Andressa, Zarbin, Paulo Henrique Gorgatti (2026): Revisiting Lamprosoma and expanding knowledge of Lychnophaes (Coleoptera: Chrysomelidae, Lamprosomatinae): Molecular phylogeny, new species, host plants, associated parasitoid wasps and geographical records. Arthropod Systematics & Phylogeny 84: 719-744, DOI: 10.3897/asp.84.e181950
A33C5698F7B15CD6A633AAF2FC388015.text	A33C5698F7B15CD6A633AAF2FC388015.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Lychnophaes imbirucu Jorge, Santos & Zarbin 2026	<div><p>5.3. 4. Lychnophaes imbirucu Jorge, Santos &amp; Zarbin sp. nov.</p><p>Figures 7, 8, 9, 10</p><p>Diagnoses.</p><p>Eyes emarginate. Scutellum tiny. Elytra covering the pygidium. The last abdominal ventrite serrated like the inner surface of the elytra (closing mechanism). Tibiae flattened. Fore and middle legs with simple claws and the hind leg with appendiculate claws.</p><p>Description.</p><p>MALE: Body. Oval, strongly convex dorsally and flat ventrally (Figs 6, 7, 8). — Integument color. Head and pronotum coppery with yellowish green reflections and elytra cyan with green reflections; ventral surface, including abdomen, dark blue; legs cyan except anterior femur with green reflections (Fig. 6). — Head. Frons with fine punctures (Figs 6 C, 7 C). Head anteriorly flat (Figs 6 D, 7 B – D). Eyes emarginated at the level of antenna insertion (Figs 6 B, 7 C). Antennae short, with eleven articles, inserted between the base, eye, and lateral edges of the clypeus (Fig. 7 C). Labrum short, transversal, narrower than the clypeus, bearing small thick setae (Fig. 7 C). — Prothorax. Pronotum convex, narrower than base of elytra, sinuous posterioly, with fine punctures like those on frons anteriorly and coarser posteriorly (Figs 6 A, 7 A); longer than wide, sinuous medially and with a truncated apex. — Mesothorax and metathorax. mesothorax small, scutellum with extremely acute apex (Figs 6 A, 7 A). Elytra with ten rows of punctures extending from the base to the apex, where they merge. In dorsal view, only eight rows are visible. Each puncture with a short seta. Epipleura narrow, with a notch for the posterior femur (Figs 6 B, 6 D, 7 B). Fore legs with femur without the inner margin projecting into the median portion, tibia without a small tooth-like in the internal and external portion apex (Figs 6 B, 7 B, 7 D). Four visible tarsomeres (Figs 7 D, 7 E); the last tarsomere protrudes less than one-third of the anterior tarsal lobe, with simple claws except for appendiculate claws in posterior legs (Fig. 7 E). Middle and posterior legs similar to anterior leg (Fig. 7 D), excepted for the transverse coxa. — Abdomen with five ventrites (Figs 6 B, 7 D), the last serrated at apex (elytral lock mechanism) (Fig. 7 F). Ventrite I with arc-shaped lateral depressions to receive metafemora; ventrites II to V medially punctate and with short setae. — Aedeagus (Fig. 9 A – D): Dorsal valve articulated, rounded at apex. Ventral margin thickened laterally, with a deep lateral emargination. — FEMALE: Similar coloration to male except for lacking metallic green spot on the profemur. In the type series, there is a single entirely coppery female with reddish reflections instead of having blue elytra as in the others (Fig. 6 E). Sternite VIII membranous, straight, without an apodeme. Genitalia (Fig. 9 E) with a circular chitinpolster, resembling Oomorphoides tonkinensis as mentioned by Schöller (2008). Styli present and articulate. Spermatheca composed of three chambers connected. Duct non-sclerotized.</p><p>Egg case.</p><p>Coverage without specific format.</p><p>Larval case.</p><p>Oval shape made up of earthy-looking material.</p><p>Host Plants.</p><p>Pseudobombax grandiflorum (Cav.) A. Robyns.</p><p>Parasitoids.</p><p>Unknown.</p><p>Geographical distribution.</p><p>Brazil: Paraná, Curitiba (Fig. 11).</p><p>Type series.</p><p>The type series of the new species of Lychnophaes comprises: the holotype and 20 paratypes, with the holotype and 18 paratypes deposited in the DZUP, and two paratypes (one ♀ and one ♂) deposited in the INPA. Seven paratypes (♀ and ♂) that were used in the molecular extraction and in the scanning electron microscope (SEM) images were also deposited in the Padre Jesus Santiago Moure Entomological Collection, totalizing 28 specimens. — DZUP. Holotype ♂ labeled: BRASIL: Paraná, Curitiba, Jardim | das Américas, Campus Jardim | Botânico, UFPR, 10. XII. 2024, | Col. Isaac R. Jorge, 2024; Consumindo Pseudobombax grandiflorum | (Cav.) | A. Robyns; HOLOTYPE | Lychnophaes imbirucu | Jorge, Santos &amp; Zarbin, 2025; DZUP | 325205 . — Two paratypes ♂ and four ♀ labeled: BRASIL: Paraná, Curitiba, Jardim | das Américas, Campus Jardim | Botânico, UFPR, 10. XII. 2024, | Col. Isaac R. Jorge, 2024; Consumindo Pseudobombax grandiflorum | (Cav.) | A. Robyns; PARATYPE | Lychnophaes imbirucu | Jorge, Santos &amp; Zarbin, 2025; DZUP | 325206; 325208; 325209; 325210; 325711; 325712 . One paratypes ♂ and seven ♀ labeled: BRASIL: Paraná, Curitiba, Jardim | das Américas, Campus Jardim | Botânico, UFPR, 01. XI. 2023, | Col. Isaac R. Jorge, Aluska T. Santos; Consumindo Pseudobombax grandiflorum | (Cav.) | A. Robyns; PARATYPE | Lychnophaes imbirucu | Jorge, Santos &amp; Zarbin, 2025; DZUP | 325255; 325253; 325254; 325256; 325257; 325258; 325259; 325260 . One paratypes ♂ and three ♀ labeled: BRASIL: Paraná, Curitiba, Jardim | das Américas, Campus Jardim | Botânico, UFPR, 01. XI. 2023, | Col. A. T. Santos &amp; Isaac R. Jorge, 2023; Consumindo Pseudobombax grandiflorum | (Cav.) | A. Robyns; PARATYPE | Lychnophaes imbirucu | Jorge, Santos &amp; Zarbin, 2025; DZUP | 325261; 325262; 325263; 325264 . One ♀ and one ♂ labeled: BRASIL: Paraná, Curitiba, Jardim | das Américas, Campus Jardim | Botânico, UFPR, 10. XII. 2024, | Col. Isaac R. Jorge, 2024; Consumindo Pseudobombax grandiflorum | (Cav.) | A. Robyns; Lychnophaes imbirucu | Jorge, Santos &amp; Zarbin, 2025 | Det. I. R. Jorge and A. T. dos Santos, 2024; DZUP | 325194; 325195; 325196; 325197; 325198; 325203; 325204 . — INPA. One paratype ♀ and one ♂ labeled: BRASIL: Paraná, Curitiba, Jardim | das Américas, Campus Jardim | Botânico, UFPR, 10. XII. 2024, | Col. Isaac R. Jorge, 2024; Consumindo Pseudobombax grandiflorum | (Cav.) | A. Robyns; PARATYPE | Lychnophaes imbirucu | Jorge, Santos &amp; Zarbin, 2025; INPA -COL 002863; INPA -COL 002864 .</p><p>Etymology.</p><p>The specific name “ imbirucu ” is a name in apposition, and it was chosen based on the host plants consumed by the species. The common name “ imbirucu ” originates from Tupi-Guarani, “ mbirusú ” language, and it’s used to name the tree belonging to the Bombacaceae, P. grandiflorum (Cav.) A. Robyns.</p><p>Remarks.</p><p>Spermatheca composed of three chambers, whereas Ly. principalis Lacordaire, 1848, possesses only two (personal observation by Isaac R. Jorge). Presence of articulate styli. Sternite VIII significantly more membranous compared to L. cambuci .</p><p>The genus Lychnophaes is distinguished from Lamprosoma only by its simple rather than appendicular claws. Since it has appendiculate claws only on the hind legs, Ly. imbirucu represents an exception to the genus. Comparative morphology studies should be performed to better understand this character.</p></div>	https://treatment.plazi.org/id/A33C5698F7B15CD6A633AAF2FC388015	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.		Pensoft via Plazi	Santos, Aluska Tavares;Jorge, Isaac Reis;Fianco, Marcos;Sampaio, Aline;Martins, André Luis;Rafael, José Albertino;Paladini, Andressa;Zarbin, Paulo Henrique Gorgatti	Santos, Aluska Tavares, Jorge, Isaac Reis, Fianco, Marcos, Sampaio, Aline, Martins, André Luis, Rafael, José Albertino, Paladini, Andressa, Zarbin, Paulo Henrique Gorgatti (2026): Revisiting Lamprosoma and expanding knowledge of Lychnophaes (Coleoptera: Chrysomelidae, Lamprosomatinae): Molecular phylogeny, new species, host plants, associated parasitoid wasps and geographical records. Arthropod Systematics & Phylogeny 84: 719-744, DOI: 10.3897/asp.84.e181950
E216AD4E7EF2510EBBECABAA390B2F19.text	E216AD4E7EF2510EBBECABAA390B2F19.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Lychnophaes Lacordaire 1848	<div><p>5.3. 3. Genus Lychnophaes Lacordaire, 1848</p><p>Lacordaire 1848: 574 (genus and species description); Chapuis 1874: 218 (catalog); Achard 1914: 4 (catalog); Blackwelder 1946: 650 (catalog); Monrós 1956: 59 (revision of the tribe, figures); Monrós 1960: 9 (catalog).</p><p>Type species.</p><p>Cryptocephalus globulosus Olivier, by subsequent designation by Achard, 1914.</p><p>Taxonomical history of Lychnophaes .</p><p>Following Lacordaire (1848), the species belonging to the Lychnophaes are easily distinguished due to the variety of colors found in the few species known, and for the Lamprosoma due to the no appendiculate claws. The nine species that were studied by Lacordaire one distributed in Brazil, five from French Guiana, one from both localities, and the last two from Colombia. Besides the color, Lacordaire divided the species into two groups based on the ocular margin. The first one was defined by the “ Eyes triangularly emarginated in the lower half ” and comported Lychnophaes laticollis, Ly. globosus, Ly. cornutus, while the second group was defined as “ Eyes quadrangularly emarginated in the lower half ”, and the following species belong to them: Ly. principalis, Ly. pilula, Ly. empyreus, Ly. hypochrysus, Ly. purpureus and Ly. cyaniceps .</p><p>Only two specimens of Lychnophaes principalis (Lacordaire, 1848) were deposited in the collection of Pe. Jesus Santiago Moure. However, the two differences observed by Lacordaire: deeply notched eyes in the lower half and triangular eyes, and slightly notched below the middle, were not observed in our material. The study of other species of the genus may better interpret this characteristic.</p></div>	https://treatment.plazi.org/id/E216AD4E7EF2510EBBECABAA390B2F19	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.		Pensoft via Plazi	Santos, Aluska Tavares;Jorge, Isaac Reis;Fianco, Marcos;Sampaio, Aline;Martins, André Luis;Rafael, José Albertino;Paladini, Andressa;Zarbin, Paulo Henrique Gorgatti	Santos, Aluska Tavares, Jorge, Isaac Reis, Fianco, Marcos, Sampaio, Aline, Martins, André Luis, Rafael, José Albertino, Paladini, Andressa, Zarbin, Paulo Henrique Gorgatti (2026): Revisiting Lamprosoma and expanding knowledge of Lychnophaes (Coleoptera: Chrysomelidae, Lamprosomatinae): Molecular phylogeny, new species, host plants, associated parasitoid wasps and geographical records. Arthropod Systematics & Phylogeny 84: 719-744, DOI: 10.3897/asp.84.e181950
