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Thrasychroma Jacoby 1885
Thrasychroma Jacoby, 1885 (Figs. 2, 3) Thrasychroma Jacoby, 1885a: 70 (type species: Thrasychroma submetallica Jacoby 1885a: 71 by monotypy). Prior to this study, two species were recognized from Indonesia: Java and Sumatra. Licyllus Jacoby, 1885b: 928 (type species: Licyllus splendidus Jacoby, 1885b: 928, by monotypy). Prior to this study, six species were recognized from Australia, New Guinea, Indonesia (Sumatra), and Vanuatu (New Hebrides). New synonymy. Material Examined. Licyllus splendidus: Cla ”…” // F. Monros collection 1959 // Licyllus splendidus // Licyllus splendidus Jac. (USNM). Thrasychroma submetallica: Sumatra Mt Singalang, Luglio 1878, O. Beccari // Thrasychroma submetallica Ws. // Dom. Mus. Civ. Genova, cotype! // Cotype // 1953 Coll. Heikertinger. (FCMB); Indonesia, Sumatra, Mt. Singalang, VII 1878. O. Beccari // F. Monros collection 1959 // Thrasychroma submetallica // Thrasychroma submetallica Jac. (USNM). Thrasychroma sp. 2 ♂♂, 3♀♀: Indonesia. Timor, Soe, 29.VI.2008, M.S. Mohamedsaid // ex. Solanum (Solanaceae) (USNM).Published as part of Lee, Chi-Feng & Konstantinov, Alexander, 1939, A New Species ofBurumoseriaCsiki, 1939 from Taiwan, with Redescription of the Genus and New Synonymy ofLicyllusJacoby, 1885 withThrasychromaJacoby, 1885 (Coleoptera: Chrysomelidae: Galerucinae: Alticini), pp. 325-331 in The Coleopterists Bulletin 1885 (2) on pages 325-331, DOI: 10.1649/0010-065X-69.2.325, http://zenodo.org/record/533241
Ivalia Jacoby
Ivalia Jacoby (Figs 1–8) Ivalia Jacoby, 1887: 100 (type species Ivalia viridipennis Jacoby 1887 designated by Maulik (1926), type locality Sri Lanka, type in BMNH). Ancyloscelis Ogloblin, 1930: 100 –101 (type species Mniophila ruficolle Motschulsky 1866 by monotypy, type locality Sri Lanka, type probably lost). Scherer, 1969: 234 (synonymy). Amphimeloides Jacoby, 1887: 95 (type species Amphimeloides dorsalis Jacoby 1887: 96 by monotypy, type locality Sri Lanka, type in BMNH). New synonym. Taizonia Chen, 1934: 182 (type species Taizonia bella Chen 1934 by original designation, type locality Taiwan, type in DEIM). New synonym. Schereria Medvedev, 1984: 60 (type species Chabria minima Scherer 1984 by original designation, type locality Nepal, holotype in NHMB). Gruev & Askevold, 1988: 140 (synonymy). Notes on generic synonymy. Based on the study of various specimens, including type specimens of the type species, we conclude that Taizonia and Amphimeloides are junior synonyms of Ivalia. They share the following character extremely rare among flea beetles: metasternum is expanded anteriorly, becoming vertical and covering mesosternum (Fig. 5 A) so the latter also becomes vertical and sometimes invisible in ventral view. This character is shared by the types of all the type species, but varies slightly among other studied species of Ivalia. In its most developed state, the character is known to occur only in Clavicornaltica Scherer (Konstantinov & Duckett 2005), also a humicole feeder but easily distinguishable from Ivalia by its clavate antennae and other features. Other uncommon characters occuring in Ivalia and some other Oriental genera include the following: a. Metatibia curved in dorsal view with long metatibial spur (Figs 1, 3 E, F), first metatarsomere as long as or longer than two following tarsomeres combined (Figs 2 D, 3 F); b. Labrum deeply emarginated (Fig. 3 A); c. Thoracic sternites with elevated processes; d. Head with frontal ridge wide and swollen together with anterofrontal ridge in one callosity (see Figs 2 C, E, 3 A–B); e. Antennal calli poorly separated from vertex and from each other, sometimes not separated at all (Figs 2 C, E, and 3 A); f. Anterolateral callosity of pronotum very long, commonly reaching midpoint of lateral margin of pronotum (Figs 1, 2); g. Vaginal palpi of female genitalia relatively short with proximal ends fused (Fig. 4 E). Overall there are no characters to separate Ivalia, Amphimeloides, and Taizonia. As Ivalia is senior to Taizonia, Ivalia remains valid and because Amphimeloides and Ivalia were published in the same paper, we here choose Ivalia as the name to use. Diagnostic characters of Ivalia. Adult beetles small to medium sized (2–5mm), convex in lateral view. Color metallic or nonmetallic dark or light shades with spots or stripes. Antennal calli poorly to moderately developed, flat to slightly raised, anterior ends somewhat triangular, entering into interantennal space, sulci surrounding antennal calli poorly developed. Eyes small, lateral, orbit narrow, antennal sockets separated by a distance subequal to two times width of orbit or more. Frontal ridge short, wide, flat to moderately raised; anterofrontal ridge wide, flat to moderately raised. Antenna hardly reaching middle of elytron, distal antennomeres widened. Labrum deeply incised. Maxillary palp long, second and third palpomeres moderately thick, distally enlarged, last pointed. Pronotum transverse, without impressions, anterior coxal cavities open behind. Elytron with irregular punctures, posteriorly narrowed; epipleuron wide, horizontal, reaching near apex. Hind wing present or absent. Thoracic sternites with raised process in middle: prosternal intercoxal process with longitudinal vertically raised ridge along middle, process on metasternum usually circular. Metacoxa greatly enlarged, ventrally with a groove and ridge for reception of femur. Metatibia in dorsal view characteristically curved with either ends directed laterally; dorsal surface with sharp lateral margin and flat mesal margin. Tarsal claw appendiculate. Vaginal palpi joined at proximal end. Spermathecal duct not coiled. Material examined. Amphimeloides dorsalis Jacoby: Holotype. Labels: 1) Type HT; 2) Ceylon, G. Lewis, 1910 – 320; 3) Dikoya, 3,800–4,200 ft. 6.XII– 16.I. 82; 4) Amphimeloides dorsalis Jac.; 5) Right hind leg mounted in balsam, S. Maulik, 1929; 6) HT found in dwr. parts missing G. A. Samuelson det. 1974 (BMNH). Ivalia viridipennis Jacoby: Syntypes male and female. Labels: 1) Ceylon, G. Lewis, 1910 – 320; 2) Dikoya, 3,800–4,200 ft. 6.XII– 16.I. 82; 3) Syntype Ivalia viridipennis Jacoby (2 BMNH). Taizonia bella Chen: Holotype male. Labels: 1) Kankau (Koshun) Formosa, H. Sauter V. 1912; 2) Holotypus; 3) Taizonia bella n. g. n. sp. S. H. Chen det. (DEIM). Schereria martensi Medvedev: Holotype male. Labels: 1) 179 a Kaski Dist., oberhalb, Dhumpus Berlese, 2100m, Martens & Ausobsky 8 / 10 Mai 80; 2) Holotypus; 3) Holotypus; 4) Schereria martensi m. L. N. Medvedev det. 1983; 5) Senckenberg Museum Frankfurt/Main (SMFM).Published as part of Duckett, Catherine N., Prathapan, K. D. & Konstantinov, Alexander S., 2006, Notes on identity, new synonymy and larva of Ivalia Jacoby (Coleoptera: Chrysomelidae) with description of a new species, pp. 49-68 in Zootaxa 1363 on pages 51-54, DOI: 10.5281/zenodo.17471
A New Species of Burumoseria Csiki, 1939 from Taiwan, with Redescription of the Genus and New Synonymy of Licyllus Jacoby, 1885 with Thrasychroma Jacoby, 1885 (Coleoptera: Chrysomelidae: Galerucinae: Alticini)
The Oriental genus Burumoseria Csiki, 1939 is redescribed. Burumoseria yuae Lee and Konstantinov, new species from Taiwan is described and illustrated. A key to Burumoseria species is provided. The Oriental and Australian genus Licyllus Jacoby, 1885 is synonymized with Thrasychroma Jacoby, 1885
Douglas Alexander Stewart, poet, author and playwright
Douglas Alexander Stewart, poet, author and playwrigh
Ivalia Jacoby 1887
IVALIA JACOBY, 1887 (FIG. 4) Type species: Ivalia viridipennis Jacoby, 1887, designated by Maulik (1926). Synonyms: Ancyloscelis Ogloblin, 1930, synonymized by Scherer (1969); Amphimeloides Jacoby, 1887, synonymized by Duckett et al. (2006); Taizonia Chen, 1934, synonymized by Duckett et al. (2006); Schereria Medvedev, 1984, synonymized by Gruev & Askevold, (1988). Phylogenetic position: The genus belongs to the Chabria group, based on both our analyses and DamaŠka et al. (2021); the latter study revealed polyphyly of the genus, therefore, the genus will require revision. Diversity and distribution: There are 86 known species of Ivalia; most species were catalogued by Nadein (2013a) listing 67 species.An additional two species were described by Medvedev (2016) and a further species by Takizawa & Konstantinov (2018). New species from the Philippines were described by DamaŠka et al. (2020) and from Japan by Takemoto & Suenaga (2021). The genus is distributed from India and the Himalayas to central China, Japan and southwards to Australia. Most species are described from high mountain ranges (Himalayas, Mt. Kinabalu and New Guinea). Revisions: The genus has not been revised recently. Duckett et al. (2006) redescribed the genus, described its larva and established new synonyms; fauna of Australia was revised by Nadein (2013a). Synoptic keys were presented by Medvedev (2009) for Indochina and Yang et al. (2015) for China and Taiwan. Morphological characteristics: The morphological features diagnosing Ivalia were proposed by Duckett et al. (2006) and should possibly be revised based on DamaŠka et al. (2021). The genus consists mainly of small to large flea beetles (1.5–5.0 mm). General body shape oval to rounded, convex in lateral view. Body colour from black, with or without metallic lustre, to yellow basic colour and variable pattern or dark elytral and pronotal spots. The majority of species are wingless. Head nearly hypognathous, antennal shape from long and slender to relatively short, with distal antennomeres somewhat widened, frontal calli poorly developed (Nadein, 2013a; Takizawa & Konstantinov, 2018). Pronotum usually about twice as wide as long, convex, on apical margins sometimes with rounded lobes visible anterolaterally. Pronotal margin with a setiferous pore situated in the apical half of the pronotal length. Procoxal cavities widely open posteriorly.The anterior process of the metaventrite expanding between the mesocoxae partially covering the mesoventrite, similar to that of Clavicornaltica and Cangshanaltica. Metaventral intercoxal process surface excavated, forming a horseshoe-shaped structure (as in Cangshanaltica). Metafemora strongly curved in many species, some described species bearing straight metafemora (Takizawa & Konstantinov, 2018). Metatibiae with a long apical spur, proximal metatarsomere elongated. Vaginal palpi fused basally, with apices widely separated. Spermatheca simply formed, with duct not bearing coils. Aedeagus usually simple with long, wide and flat apex. Ecology: In most species the ecology is not known, but all species with known biology are associated with mosses and known larvae feed on mosses (Duckett et al., 2006; Takizawa & Konstantinov, 2018; Takemoto & Suenaga, 2021). The majority of known species are described from high elevations up to 3500 m, but mid-elevation and lowland species are known as well (DamaŠka & Aston, 2019; Takemoto & Suenaga, 2021). Remarks: Diagnoses from Clavicornaltica and Cangshanaltica were mentioned above. Ivalia is also similar to Phaelota Jacoby, 1887, from which it can be distinguished by the morphology of procoxal cavities, closed posteriorly in Phaelota, open in Ivalia (Konstantinov et al., 2013).Published as part of Damaška, Albert František, Konstantinov, Alexander & Fikáček, Martin, 2022, Multiple origins of moss-inhabiting flea beetles (Coleoptera: Chrysomelidae): molecular phylogeny, overview of genera and a new genus from Africa, pp. 647-676 in Zoological Journal of the Linnean Society 196 on page 663, DOI: 10.1093/zoolinnean/zlab112, http://zenodo.org/record/719624
New Alexander Drug Company
Photograph of the New Alexander Drug Company Building at Northeast 12th Street and Oklahoma Street, Oklahoma City, OK
Phaelota Jacoby 1887
PHAELOTA JACOBY, 1887 (FIG. 4) Type species: Phaelota semifasciata Jacoby, 1887. Synonymy: This genus has no generic synonyms. Phylogenetic position: Unknown. A possible placement in the Chabria group has been discussed, but no molecular or morphological phylogenetic analysis has been published to justify this. Diversity and distribution: So far, 16 species of Phaelota are known (Ruan et al., 2017). The genus is found mainly in India and Sri Lanka. One species was described from Borneo (Konstantinov, 2008). Revisions: The fauna of southern India and Sri Lanka was recently revised by Prathapan & Viraktamath (2009). Morphological characteristics: Body large, 2.5 to 5.5 mm long, oval to round in dorsal view, moderately convex in lateral view, colour variable. Head hypognathous, partially retracted into prothorax. Antennal calli well developed, triangular, separated from vertex and from each other by deep impressions. Frontal ridge wide and flat. Antennae with 11 antennomeres, not widened or forming any apical club. Pronotum wide, with a feebly developed a n t e b a s a l t r a n s v e r s e i m p r e s s i o n, s u r r o u n d e d by two short longitudinal impressions. Procoxal cavities closed posteriorly; in Phaelota sindhoori Prathapan & Viraktamath, 2004, procoxal cavities narrowly open. The intercoxal proventral process wide. Elytra narrowing towards apex, with rows of slightly developed punctures. Legs long; all coxae with a triangular posterior denticle. Aedeagus simple, slightly curved in lateral view. Spermatheca simple, with a long pump and bulbous receptacle; spermathecal duct without coils. Vaginal palpi fused basally, and parallel. Ecology: The genus contains both moss-inhabiting and leaf-surface-living species (Konstantinov et al., 2013; Ruan et al., 2017). Prathapan & Viraktamath (2009) report that at least three leaf-surface-living Indian species feed on ferns. It is likely that various species from the genus feed on various food sources; however, the ecology of Phaelota needs more research to be resolved. Remarks: The genus is similar to Chabria and Acrocrypta Baly, 1862. It can be separated from Chabria, by having closed procoxal cavities (procoxal cavities are open in Chabria). From Acrocrypta, the genus differs by having a wide intercoxal proventral process and elytral punctures in rows (in Acrocrypta, the intercoxal proventral process is narrow and elytra are confusedly punctured).Published as part of Damaška, Albert František, Konstantinov, Alexander & Fikáček, Martin, 2022, Multiple origins of moss-inhabiting flea beetles (Coleoptera: Chrysomelidae): molecular phylogeny, overview of genera and a new genus from Africa, pp. 647-676 in Zoological Journal of the Linnean Society 196 on pages 668-669, DOI: 10.1093/zoolinnean/zlab112, http://zenodo.org/record/719624
FIGURE 1 in Notes on identity, new synonymy and larva of Ivalia Jacoby (Coleoptera: Chrysomelidae) with description of a new species
FIGURE 1. Dorsal habitus of Ivalia korakundah new species, total body length 1.8 mm.Published as part of Duckett, Catherine N., Prathapan, K. D. & Konstantinov, Alexander S., 2006, Notes on identity, new synonymy and larva of Ivalia Jacoby (Coleoptera: Chrysomelidae) with description of a new species, pp. 49-68 in Zootaxa 1363 on page 53, DOI: 10.5281/zenodo.17471
Author inscription in William Hazlitt, essayist and critic; selections from his writings, with a memoir, biographical and critical by Alexander Ireland
Author's gift inscription, "To W. C. Hazlitt Esq with kind regards, from Alexr Ireland," with tipped-in review of the book.ASU Library edition has inscription from Ireland to Hazlitt [a child of William Hazlitt?].
Hazlitt , William, 1778-1830.
Ireland, Alexander, 1810-1894
Chaetocnema (Chaetocnema) granulicollis Jacoby 1896
16. Chaetocnema (Chaetocnema) granulicollis Jacoby, 1896 (Fig. 36) Chaetocnema granulicollis Jacoby, 1896: 439. TL: Sumatra. TD: BMNH. Lectotype designated here. Chaetocnema flavipennis Medvedev, 1996: 68. TL: Philippines (Luzon, Mount Makiling). TD: Medvedev Collection. (Syn. Nov.) Distribution: Malaysia, Singapore, Philippines (Medvedev, 1996), Indonesia (Sumatra), India. Host plants: Unknown. Description: Body length: 1.70–1.90 mm. Body width: 1.00– 1.10 mm. Ratio of elytron length (along suture) to width (maximum): 2.15–2.25. Ratio of pronotum width (at base) to length: 1.80–1.90. Ratio of length of elytron to length of pronotum (along middle): 2.40–2.50. Ratio of width of elytra at base (in middle of humeral calli) to width of pronotum at base: 1.05–1.10. Color variable, typical individuals have yellow elytra with brown area near scutellum, or elytra entirely brown in some cases. Head and pronotum bronzy to brown. Antennomeres 1–5 yellow brown, 6–11 brown. Tibiae yellow brown. Pro- and mesofemora light brown. Metafemora dark brown. Pronotum and head rugose. Head hypognathous. Frontal ridge wide, slightly convex. Frontolateral sulcus present. Suprafrontal sulcus shallow laterally, deep in middle. Orbital sulcus deep and straight. Ratio of width of frontal ridge (excluding margin) to width of antennal socket (excluding margin): 2.95–3.00. Number of punctures on vertex: 60–90, punctures sometimes extremely weak. Number of punctures on orbit: 1–2 on each side. Number of punctures on frons (triangular area surrounded by frontolateral sulcus and clypeus): 0. Number of setae on clypeus: 13. Number of setae on labrum: 6. Anterior margin of labrum slightly convex at middle. Base of pronotum without short longitudinal impressions near basal margin, with deep row of large punctures at sides, weak in some specimens. Pronotal base slightly convex, with middle prominently expanded. Lateral margins of pronotum nearly straight, converging forward with maximum width near base. Anterolateral prothoracic callosity strongly developed, forming obtuse angle laterally. Posterolateral prothoracic callosity poorly developed. Diameter of pronotal punctures 2 to 3 times smaller than distance between them. Elytra with slightly convex lateral sides. All rows of elytral punctures regular and single. Interspaces between rows of punctures smooth and glabrous except the few near scutellum are rugged. Humeral callus well developed. First male protarsomere slightly larger than second. Excavation of hind tibia moderately deep. Large lateral denticle on metatibia sharp. Metatibial serration proximal to large lateral denticle absent. Apex of aedeagus unique, arrow-head shaped in ventral view. Ventral longitudinal groove absent. Apical denticle in ventral view absent. Minute transverse wrinkles on ventral side absent. Aedeagus in lateral view unevenly curved, apex sinusoidal. Maximum curvature in lateral view situated near apex. Spermathecal receptacle pear-shaped. Basal part of spermathecal duct coiled. Spermathecal pump much shorter than receptacle, with cylindrical apex. Receptacle basally wider than apically. Apex of vaginal palpus rounded, with slightly convex lateral margin. Anterior end of anterior sclerotization evenly rounded. Posterior sclerotization longer than wide. Both width and length of posterior sclerotization greater than that of anterior sclerotization. Types: Lectotype: 1♂ (BMNH), labels: 1) Type H.T.; 2) Sumatra Siboga X.90 – III.91 E. Modigliani; 3) Jacoby Coll. 1909–28 a; 4) Chaetocnema granulicollis Jac.; 5) Lectotype Chaetocnema granulicollis Jacoby, 1896 Des. Ruan et al., 2016. Paralectotype: 3♀ (BMNH), labels: 1) Sumatra Balighe X.90 – III.91 E. Modigliani; 2) Jacoby Coll. 1909–28 a.; 3) Lectotype Chaetocnema granulicollis Jacoby, 1896 Des. Ruan et al., 2016. Material: 1♀ (USNM), Malaysia, Sabah, 7km NNW Kudat, Tanjung Tajau, 19.IX.1983, loan from USNMNH 2065634; 1♂ (BMNH), Sarawak (Malaysia), on vegetable, 8–vii–63, coll. S. KUEH, Chaetocnema granulicollis Jacoby, 1896, Det. Yongying Ruan, 2016; 1♂ (BMNH), Singapore, C. J. Saunders, B.M. 1933–227, Chaetocnema granulicollis Jacoby, 1896, Det. Yongying Ruan, 2016; 3♂ 1♀ (USNM), India, Assam Chabua, 20.II.1944, D. E. Hardy, loan from USNMNH 2065634; 1♂, Chabua, Assam, India, 2–X–43, DEHardy, Chaetocnema flavipennis Medvedev, 1996 det. Yongying Ruan, 2016. Remarks: Specimens of C. granulicollis, even from the same locality, vary greatly. For instance, the general color of elytra vary from yellow to dark brown; punctation of head and pronotum range from weak to strong and even the shape of the apex of aedeagus may vary slightly.Published as part of Ruan, Yongying, Yang, Xingke, Konstantinov, Alexander S., Prathapan, Kaniyarikkal D. & Zhang, Mengna, 2019, Revision of the Oriental Chaetocnema species (Coleoptera, Chrysomelidae, Galerucinae, Alticini), pp. 1-206 in Zootaxa 4699 (1) on pages 59-61, DOI: 10.11646/zootaxa.4699.1.1, http://zenodo.org/record/354303
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