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Journal articles on the topic 'Taprobane'

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Author: Grafiati
Published: 10 March 2023

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1

Jang, Sieun. "In Search of Taprobane - ‘Taprobane’ in Ancient Greek Texts -." Association of Korean Cultural and Historical Geographers 33, no. 1 (April 30, 2021): 52–68. http://dx.doi.org/10.29349/jchg.2021.33.1.52.

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2

Hanima, R. K. P., P. G. Kumar, and V. D. Hegde. "New record of Methocha (Dryinopsis) taprobane Krombein, 1982 (Hymenoptera: Tiphiidae, Methochinae) from India." Far Eastern entomologist 450 (March 2, 2022): 12–14. http://dx.doi.org/10.25221/fee.450.3.

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3

Abeydeera, Ananda. "Taprobane, Ceylan ou Sumatra? Une confusion féconde." Archipel 47, no. 1 (1994): 87–124. http://dx.doi.org/10.3406/arch.1994.2970.

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4

Abeydeera, Ananda. "Encore Taprobane. A Propos du témoignage tardif de Thomaso Porcacchi (1576)." Archipel 49, no. 1 (1995): 125–36. http://dx.doi.org/10.3406/arch.1995.3039.

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5

Lee, Eun Seon. "Cosmas’ Awareness of Christian Expansion in Christian Topography and Taprobane." Journal of Youngsan Theology 52, no. 01 (June 30, 2020): 39–76. http://dx.doi.org/10.18804/jyt.2020.06.52.39.

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6

Ducœur, Guillaume. "Clément d’Alexandrie et les Semnoí de Taprobane. Remarques sur Stromates 3.7.60.3‑4." Revue de l'histoire des religions, no. 235 (September 1, 2018): 379–414. http://dx.doi.org/10.4000/rhr.8927.

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7

Abeydeera, Ananda. "Encore Taprobane. Giovanni Battista Ramusio y voit Sumatra et Immanuel Kant Madagascar." Archipel 56, no. 1 (1998): 199–230. http://dx.doi.org/10.3406/arch.1998.3486.

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8

Habib, Irfan. "Book Review: Osmund Bopearachchi, From Bactria to Taprobane: Selected Works of Osmund Bopearachchi, Vol. I: Central Asian and Indian Numismatics." Studies in People's History 2, no. 1 (May 24, 2015): 136–38. http://dx.doi.org/10.1177/2348448915574376.

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9

Meyer, Eric. "Tagus to Taprobane: Portuguese Impact on the Socio-culture of Sri Lanka from 1505 AD. By Shihan de Silva Jayasuriya. pp. 459. Dehiwala (Sri Lanka), Tisara Prakasakayo, 2001." Journal of the Royal Asiatic Society of Great Britain & Ireland 16, no. 1 (March 15, 2006): 99. http://dx.doi.org/10.1017/s1356186305285917.

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10

MLYNAREK, JULIA J., and TERRY A. WHEELER. "Phylogeny and revised classification of the tribe Elachipterini (Diptera: Chloropidae)." Zootaxa 4471, no. 1 (September 4, 2018): 1. http://dx.doi.org/10.11646/zootaxa.4471.1.1.

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The phylogenetic relationships of the chloropid tribe Elachipterini were analysed. Sixty-eight exemplar species and seven outgroup species were included in a cladistic analysis based on 76 morphological characters of adult specimens in order to test existing, non-phylogenetic, classifications of the tribe. Nine genera are recognized in the Elachipterini: Allomedeia Mlynarek & Wheeler, Alombus Becker, Anatrichus Loew, Ceratobarys Coquillett, Disciphus Becker, Elachiptera Macquart, Goniaspis Duda, Melanochaeta Bezzi and Sepsidoscinis Hendel. Myrmecosepsis Kertesz is synonymised with Anatrichus, and Togeciphus Nishijima and Cyrtomomyia Becker are synonymised with Elachiptera. Ceratobarys is removed from synonymy with Elachiptera and all Neotropical species and two Nearctic species previously assigned to Elachiptera are transferred to Ceratobarys. Melanochaeta is a valid genus; the type species Melanochaeta capreolus clusters with other species of Melanochaeta and not Oscinella. New combinations include Anatrichus hystrix (Kertesz, 1914) (Myrmecosepsis); Anatrichus taprobane (Andersson, 1977) (Myrmecosepsis), Ceratobarys attenuata (Adams, 1908) (Elachiptera); Ceratobarys cultrata (Wheeler & Forrest, 2002) (Elachiptera); Ceratobarys flavida (Williston, 1896) (Elachiptera); Ceratobarys melinifrons (Mlynarek & Wheeler, 2008) (Elachiptera); Ceratobarys fucosa (Mlynarek & Wheeler, 2008) (Elachiptera); Ceratobarys queposana (Mlynarek & Wheeler, 2008) (Elachiptera); Ceratobarys rubida (Becker, 1912) (Elachiptera); Ceratobarys sacculicornis (Enderlein, 1911) (Elachiptera); Ceratobarys willistoni (Sabrosky, 1948) (Elachiptera), Elachiptera ensifer (Sabrosky, 1951) (Cyrtomomyia); Elachiptera ericius (Kanmiya, 1983) (Togeciphus); Elachiptera katoi (Nishijima, 1955) (Togeciphus); Elachiptera maculinervis (Becker, 1910) (Cyrtomomyia); Elachiptera punctulata (Becker, 1912) (Cyrtomomyia); Elachiptera subelongata (Kanmiya, 1983) (Disciphus); Elachiptera truncatus (Liu & Yang, 2012) (Togeciphus); Elachiptera tuberculata (Adams, 1905) (Cyrtomomyia) and all the species that were placed in Lasiochaeta are returned to Melanochaeta. A key to genera of the tribe Elachipterini is provided and diagnoses are provided for all genera. The tribe is divided into two geographically distinct clades: the Anatrichus clade includes the Old World tropical genera Allomedeia, Alombus, Anatrichus, Disciphus and Sepsidoscinis; the Elachiptera clade includes the primarily Neotropical genera Goniaspis and Ceratobarys and the widespread, but primarily Holarctic, genera Elachiptera and Melanochaeta.
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11

Viswanath, T. K., and V. D. Hegde. "First record of Boletoxenus taprobanae (Lewis, 1894) (Coleoptera: Tenebrionidae) from India." Far Eastern entomologist 469 (January 8, 2023): 26–28. http://dx.doi.org/10.25221/fee.469.5.

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12

VOLYNKIN, ANTON V. "Three new species of the genus Aemene Walker (Lepidoptera: Erebidae: Arctiinae) from the Himalayas." Zootaxa 5068, no. 4 (November 18, 2021): 533–46. http://dx.doi.org/10.11646/zootaxa.5068.4.4.

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Three new species of the genus Aemene Walker, 1854 are described: Aemene cernyi sp. n. (NE India and E Nepal), Aemene laszloi sp. n. (C Nepal) and Aemene bucseki sp. n. (C Nepal and Pakistan). The Aemene taprobanis Walker, 1854 species-group is established and characterised. The status of one taxon previously considered as a junior synonym of A. taprobanis is revised: Aemene sinuata Moore, 1878, stat. rev. A taxon previously considered as a subspecies of A. taprobanis is upgraded to species level: Aemene likiangensis (Daniel, 1951), stat. nov. Lectotypes are designated for Aemene taprobanis Walker, 1854, Panassa cingalesa Walker, 1865, Autoceras grammophora Felder, 1874 and Aemene sinuata Moore, 1878. Adults together with the male and the female genitalia of the new and related species are illustrated.
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13

Camilo, Vagner. "Meyer, do Arpoador a muito além da Taprobana." Alea : Estudos Neolatinos 19, no. 2 (May 2017): 339–55. http://dx.doi.org/10.1590/10.1590/1517-106x/2017192339355.

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Resumo O objetivo deste artigo é examinar a “Elegia do Arpoador”, incluída nos Últimos poemas (1955), de Augusto Meyer, juntamente com seu estudo sobre Camões, o bruxo e o diálogo que ela institui com certa tendência neoclássica marcante na lírica brasileira dos anos 1940 e 1950.
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14

Ustjuzhanin, Petr, Vasiliy Kovtunovich, Viktor Sinyaev, and Alexander Streltzov. "Fauna of Pterophoridae (Lepidoptera) of Sierra Leone (Western Africa)." Ecologica Montenegrina 35 (October 9, 2020): 26–30. http://dx.doi.org/10.37828/em.2020.35.3.

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The faunal review of Pterophoridae species is given for the fauna of Sierra Leone for the first time the type localities and world distribution (with new data) are specified. The information on the collected materials is given. Eleven species, previously unknown for this territory – Ochyrotica africana, Platyptilia farfarella, Bipunctiphorus dimorpha, Stenoptilodes taprobanes, Sphenarches erythrodactylus, Exelastis pumilo, E. tenax, E. vuattouxi, Hellinsia madecasseus, Pterophorus albidus and P. lampra – are added to the two known Pterophoridae species of Sierra Leone (Megalorhipida leucodactylus and Pterophorus candidalis).
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15

D’Angelis, Wagner Rocha. "Indo Além da Taprobana: O Instituto da Supranacionalidade no Mercosul." REVISTA INTERNACIONAL CONSINTER DE DIREITO 14, no. 14 (June 30, 2022): 491–511. http://dx.doi.org/10.19135/revista.consinter.00014.23.

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Celebrating thirty years of existence on 03/26/2021, the MERCOSUR Bloc has not yet managed to transform itself into a common market – the main objective for which it was designed, as stated in Article 1 of its foundation milestone, the Treaty of Asuncion (1991). Having achieved comercial success as a free trade zone, but proving to be ambiguous and imperfect in its version of a customs union, the bloc gestated in Asuncion, Paraguay, has shown notable advances and several setbacks, as it is subject to the misfortunes and political glimpses of its governments – in addition to the difficulties arising from the world economic order and amplified due to the COVID-19 pandemic – owing to the fact that, to this day, it has been kept under the criterion of intergovernability. However, the MERCOSUR is still considered a strong mechanism for positive commercial and social contributions among its partners. As a regional reality or even as a strategic idea, the model maintains its strenght, its validity and a good support base, enabling it for better times to come. In order to do so, however, it is essential that member countries open themselves to the idea of shared integration along the lines of the European Union, concluding the convergence period of the common external tariff (CET) and opting for an integration governed by the institute of supranationality, with its acts and functioning subject to a supranational Court of Justice. Therefore, the main objectives of this study are to shed a light on the internal order obstacles of its member states to achieve the referred purpose, and to present the necessary adjustments to upgrade the association towards the common market – where institutional rules as well as human and social rights can really prevail.
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16

LI, JUNLAN, CUIQING GAO, and WENJUN BU. "Review of the tribe Lethaeini Stål (Hemiptera: Heteroptera: Lygaeoidea: Rhyparochromidae) from China, with a key to Chinese genera and species." Zootaxa 3126, no. 1 (December 12, 2011): 28. http://dx.doi.org/10.11646/zootaxa.3126.1.2.

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The tribe Lethaeini Stål from China is reviewed. Seventeen species in seven genera are recognized. Four genera, Adauctus Distant, Atkinsonianus Distant, Lamproceps Reuter, and Lethaeus Dallas; and five species, Adauctus cupreus Distant, Atkinsonianus reticulatus Distant, Lamproceps antennatus (Scott), Lamproceps bipunctatus (Bergroth), and Lethaeus taprobanes Kirkaldy are reported for the first time from China (new records). Diniella yinae Zheng & Liu is treated as a junior synonym of Lamproceps antennatus (Scott) (new synonymy). A key to Chinese genera and species of the tribe is given. Diagnoses of the genera, habitus photos, male genitalia illustrations, additional distributions, biology (if possible), and taxonomic remarks of the species are also presented.
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17

KLUGE, NIKITA J., M. VASANTH, C. BALASUBRAMANIAN, and K. G. SIVARAMAKRISHNAN. "Review of the Kimminsula-complex (Ephemeroptera, Leptophlebiidae)." Zootaxa 5212, no. 1 (November 22, 2022): 1–140. http://dx.doi.org/10.11646/zootaxa.5212.1.1.

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Distribution of the Kimminsula complex is limited by mountains of the Western Ghats in India and the Central Highlands in Sri Lanka. Indian taxa include the new genus Ghatula gen. n. with 2 new species, Ghatula rufa sp. n. (type species of Ghatula, described here from larvae of both sexes, female subimago, female imago and eggs associated by rearing) and Ghatula quadrimaculata sp. n. (described here from larvae of both sexes); and the genus Petersula Sivaramakrishnan 1984 with type species Petersula courtallensis Sivaramakrishnan 1984 (additionally described here from larvae of both sexes, female subimagines, female imagines and eggs associated by rearing), Petersula heptagenoides sp. n. (described here from larvae, subimagines, imagines of both sexes and eggs associated by rearing) and Petersula nathani Sivaramakrishnan & Hubbard 1984 (known as a single male imago). In Sri Lanka the Kimminsula complex is represented by the following taxa: the new genus Ceylonula gen. n. with the single species Ceylonula femoralis (Hagen 1858) comb. n. (originally in Potamanthus; redescribed here from larvae, subimagines, imagines of both sexes and eggs associated by rearing); the genus Kimminsula Peters & Edmunds 1970 with type species Kimminsula taprobanes (Walker 1853) [= Kimminsula annulata (Hagen 1858)] (redescribed here from larvae, subimagines, imagines of both sexes and eggs associated by rearing), Kimminsula fasciata (Hagen 1858) (redescribed here from larvae, subimagines, imagines of both sexes and eggs associated by rearing), Kimminsula podi sp. n. (described here from larvae, male subimagines, male imagines and eggs associated by rearing) and Kimminsula latifolia sp. n. (described here from larvae); a form intermediate between K. fasciata and K. taprobanes is described here from larvae, subimagines, imagines of both sexes and eggs associated by rearing; and the new genus Hubbardula gen. n. with the single species Hubbardula heterolepida sp. n. (described here from larvae, subimagines, imagines of both sexes and eggs associated by rearing). Systematic position of the Kimminsula-complex is discussed.
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18

Ustjuzhanin, P. Ya, V. N. Kovtunovich, R. V. Yakovlev, and A. N. Streltzov. "Materials on the Lepidoptera fauna of “Ecoportal de Piedra” National Park (Jujuy Province, North-Western Argentina). Part I. Pterophoridae (Lepidoptera: Pterophoridae)." SHILAP Revista de lepidopterología 49, no. 195 (September 30, 2021): 435–46. http://dx.doi.org/10.57065/shilap.282.

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Basing on the materials from Russian entomological expedition to Jujuy Province, North-Western Argentina, the participants of which were working in Ecoportal de Piedra National Park, 22 Pterophoridae species have been revealed, two of which, Emmelina doroshkini Ustjuzhanin & Kovtunovich sp. n. and E. reshetnikovi Ustjuzhanin & Kovtunovich sp. n., turned to be new to Science. Six more species, Bipunctiphorus nigroapicalis (Landry & Gielis, 1992), Stenoptilodes brevipennis (Zeller, 1874), S. taprobanes (Felder & Rogenhofer, 1875), Lioptilodes cuzcoicus Gielis, 1996, Adaina zephyria Barnes & Lindsey, 1921, and Hellinsia mauleicus (Gielis, 1991) have been indicated for Argentina for the first time, and eleven more species, Postplatyptilia flinti Gielis, 1991, Stenoptilodes sematodactyla (Berg, 1885), Lioptilodes aguilaicus Gielis, 1991, Oidaematophorus pseudotrachyphloeus Gielis, 2011, Singularia carabayus (Arenberger, 1990), Hellinsia angulofuscus (Gielis, 1991), H. chalupi Gielis, 2013, H. grandaevus (Meyrick, 1931), and H. tacanasensis Gielis, 2013 have been indicated for Jujuy Province for the first time. One species of the genus Singularia has not been identified on a unique female.
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19

Gildenkov, M. Yu. "Seven new species of the genus Carpelimus Leach, 1819 from the “taprobanae” group (Coleoptera: Staphylinidae: Oxytelinae)." Russian Entomological Journal 28, no. 1 (September 2019): 138–45. http://dx.doi.org/10.15298/rusentj.28.2.04.

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20

EGUCHI, KATSUYUKI. "A revision of Northern Vietnamese species of the ant genus Pheidole (Insecta: Hymenoptera: Formicidae: Myrmicinae)." Zootaxa 1902, no. 1 (October 15, 2008): 1–118. http://dx.doi.org/10.11646/zootaxa.1902.1.1.

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Northern Vietnamese species of the ant genus Pheidole (Myrmicinae: Pheidolini) were revised, and 31 species including six new species were recognized: capellinii Emery, colpigaleata Eguchi, dugasi Forel, elongicephala sp.n., fervens F. Smith, fervida F. Smith, fortis Eguchi, foveolata Eguchi, gatesi (Wheeler), hongkongensis Wheeler, indosinensis Wheeler stat.n., laevicolor Eguchi, laevithorax sp.n., magna Eguchi, megacephala (Fabricius), noda F. Smith, ochracea sp.n., parva Mayr, pieli Santschi, plagiaria F. Smith, planifrons Santschi, rabo Forel, rugithorax sp.n., smythiesii Forel, taipoana Wheeler, tjibodana Forel, tumida sp.n., vieti sp.n., vulgaris Eguchi, yeensis Forel, zoceana Santschi. The following cases of synonymy were resolved: Myrmica agilis F. Smith as a junior synonym of Pheidole megacephala; Pheidole rhombinoda var. stella Forel, P. rhombinoda var. formosensis Forel, P. rhombinoda var. taprobanae Forel, and P. nodus var. flebilis Santschi as junior synonyms of P. noda; Pheidole peguensis r. yomensis as a junior synonym of P. plagiaria; and Pheidole smythiesii var. bengalensis Forel and P. bhavanae Bingham as junior synonyms of P. smythiesii. The lectotype was designated for the following species: Pheidole dugasi, P. rhombinoda var. stella, P. peguensis r. yomensis and P. sulcaticeps r. yeensis. A key to N. Vietnamese species of Pheidole based on the worker caste is given.
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21

Ustjuzhanin, P. Ya, A. A. Teimurov, V. V. Anikin, A. Yu Matov, A. E. Naydenov, A. N. Streltsov, and R. V. Yakovlev. "Materials on the Lepidoptera fauna of the Dagestan Republic (Northeastern Caucasus, Russia): autumn aspect (Insecta: Lepidoptera)." SHILAP Revista de lepidopterología 50, no. 198 (June 30, 2022): 213–28. http://dx.doi.org/10.57065/shilap.125.

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The article provides the list of Lepidoptera (the families: Cossidae, Coleophoridae, Choreutidae, Ethmiidae, Pterophoridae, Pyralidae, Crambidae, Lemoniidae, Lasiocampidae, Drepanidae, Geometridae, Sphingidae, Erebidae, Noctuidae, Lycaenidae, Nymphalidae, Pieridae), collected in four localities in the Republic of Dagestan in September 2020. In total, 207 species have been recorded. Five species are reported for the fauna of Russia for the first time: Casignetella texanella (Chambers, 1878) (Coleophoridae), Agriphila cyrenaicellus (Ragonot, 1887), Thyridiphora furia (Swinhoe, 1884), Haritalodes derogata (Fabricius, 1775) (Crambidae), and Scopula minorata (Boisduval, 1833) (Geometridae); 23 species - for the fauna of Eastern Caucasus: Perygra glaucicolella (Wood, 1892), Ecebalia halophilella (Zimmermann, 1926), E. linosyris (E. Hering, 1937), Ionescumia clypeiferella (O. Hofmann, 1871), Carpochena trientella (Christpoh, 1872) (Coleophoridae), Tebenna micalis (Mann, 1857) (Choreutidae), Ethmia candidella (Alpheraky, 1908) (Ethmiidae), Stenoptilia zophodactyla (Duponchel, 1838), Stenoptilodes taprobanes (Felder & Rogenhofer, 1875), Crombrugghia laetus (Zeller, 1847) (Pterophoridae), Glyptoteles leucacrinella Zeller, 1848, Cadra calidella (Guenée, 1845), (Pyralidae), Agriphila selasella (Hübner, [1813]), Agriphila tolli (Bleszynski, 1952), Agriphila poliellus (Treitschke, 1832), Pediasia contaminella (Hübner, 1796), Pediasia fascelinella (Hübner, [1813]), Uresiphita gilvata (Fabricius, 1794), Antigastra catalaunalis (Duponchel, 1833) (Crambidae), Watsonalla binaria (Hufnagel, 1767) (Drepanidae), Idaea degeneraria erschoffi (Christoph, 1872), Scopula nigropunctata (Hufnagel, 1767), and Rhodometra sacraria (Linnaeus, 1767) (Geometridae).
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22

SABU, THOMAS K., PRABHAKAR ABHITHA, and DANYANG ZHAO. "A new Helluodes Westwood species from Western Ghats with notes on habitat, distribution and phylogenetic relationships of genera Helluodes Westwood and Physocrotaphus Parry of the tribe Physocrotaphini Chaudoir (Insecta: Coleoptera: Carabidae: Anthiinae)." Zootaxa 1745, no. 1 (April 9, 2008): 30. http://dx.doi.org/10.11646/zootaxa.1745.1.3.

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Description of Helluodes devagiriensis, n.sp. from western slopes of the Western Ghats, a global biodiversity hot spot in southwest India, is provided along with redescriptions of all species of Helluodes Westwood and Physocrotaphus Parry (H. taprobanae Westwood, H. westwoodi Chaudoir, Physocrotaphus ceylonicus Parry), keys to the genera of tribe Physocrotaphini and the species of genus Helluodes, notes on a curious sexually dimorphic character of species in the tribe and on termitophilous and geophilous habits of genus Helluodes, a discussion of the geographic distribution and phylogenetic relationships of the genera, and supportive evidence for the divergence of Physocrotaphini Chaudoir from Zuphiini Bonelli. Based on distributional patterns and phylogenetic relationships, (1) origin of the tribe in the southwest region of the Greater Indian Plate is hypothesized with Helluodes as basal stock; (2) Helluodes is endemic to the Western GhatsSri Lanka global hot spot of biodiversity; (3) Physocrotaphus is endemic to the globally outstanding montane evergreen forest ecoregion of Sri Lanka; (4) Pogonoglossus Chaudoir is a derivative of the Helluodes ancestral stock that dispersed into southeast Asia and beyond before Deccan trap formation; and (5) Physocrotaphus is a later derivative of the Helluodes stock after the separation of Sri Lanka from the Indian mainland.
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23

GUÉORGUIEV, BORISLAV, and HONGBIN LIANG. "Revision of the Palaearctic and Oriental representatives of Lachnocrepis LeConte and Oodes Bonelli (Coleoptera: Carabidae), with special account on Chinese species." Zootaxa 4850, no. 1 (September 8, 2020): 1–89. http://dx.doi.org/10.11646/zootaxa.4850.1.1.

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In order to investigate the Chinese representatives from two genera of the tribe Oodini LaFerté-Sénectère, 1851, twenty-three Palaearctic and Oriental species of the genera Lachnocrepis LeConte, 1853 and Oodes Bonelli, 1810 are taxonomically reviewed. Because the species in question share a high degree of morphological similarity they are grouped in the “Oodes generic group”. The character-analysis showed that seven species belong to Oodes, including five species to Oodes s.str. and two species to Lachnocrepis (downgraded to subgenus). The remaining sixteen species are classified in three genera: ten species in Pseudoodes gen. n. (type species: Oodes cribristernis Bates, 1892), two species in Sundaoodes gen. n. (type species: Sundaoodes hainanensis sp. n.), and four species in Nothoodes gen. n. (type species: Oodes angustatus Lorenz, 2005). The taxa of Oodes s.str. and Pseudoodes gen. n. are arranged in two and four species groups, respectively. Eleven species from three genera, including six new to science, are found in China: Oodes (Oodes) echigonus Habu & Baba, 1960, Oodes (Lachnocrepis) desertus Motschulsky, 1858, Oodes (Lachnocrepis) japonicus (Bates, 1873), Pseudoodes cribristernis (Bates, 1892) (first record for China), Pseudoodes rambouseki (Jedlička, 1931), Pseudoodes ampliusculus, sp. n. (type locality: Mingfenggu Valley, Jiangfengling Mountains, Hainan), Pseudoodes emeishanicus, sp. n. (type locality: Xixinsuo Temple, Emei Shan, Leshan City, Sichuan), Pseudoodes hunanensis, sp. n. (type locality: Xiaozhuangping, Tianping Shan, Sangzhi County, Hunan), Pseudoodes leigongshanicus, sp. n. (type locality: Xijiang Town, Leigong Shan, Leishan County, Guizhou), Pseudoodes tianlinensis, sp. n. (type locality: Cenwanglao Shan, Tianlin County, Guangxi), and Sundaoodes hainanensis, sp. n. (type locality: Nada Town, Danzhou City, Hainan). Two further new species, Sundaoodes kalimantanensis, sp. n. (type locality: Bukit Liang Mount, West Kalimantan Province, Indonesia) and Nothoodes bharat, sp. n. (type locality: Dwarakapuram Village, Naidupet Mandal, Nellore District, Andhra Pradesh, India), are also described. The following new synonymies are proposed: Oodes parallelus Motschulsky, 1858, syn. n. of Oodes helopioides (Fabricius, 1792); Oodes parallelogrammus Motschulsky, 1858, syn. n. of Oodes helopioides (Fabricius, 1792); Oodes prolixus Bates, 1873, syn. n. of Oodes desertus Motschulsky, 1858; Simous viridissimus Louwerens, 1951, syn. n. of Pseudoodes coelestinus (Chaudoir, 1882). The synonymy of Oodes hahni Reitter, 1908 with Oodes desertus Motschulsky, 1858 is confirmed. Also, the following new combinations are introduced: Oodes japonicus (Bates, 1873), comb. n. of Lachnocrepis japonica Bates, 1873; Pseudoodes vicarius (Bates, 1873), comb. n. of Oödes vicarius Bates, 1873; Pseudoodes coelestinus (Chaudoir, 1882), comb. n. of Oodes coelestinus Chaudoir, 1882; Pseudoodes subcoriaceus (Chaudoir, 1882), comb. n. of Oodes subcoriaceus Chaudoir, 1882; Pseudoodes cribristernis (Bates, 1892), comb. n. of Oodes cribristernis Bates, 1892; Pseudoodes rambouseki (Jedlička, 1931), comb. n. of Holosoma rambouseki Jedlička, 1931; Nothoodes taprobanae (Andrewes, 1923), comb. n. of Oodes taprobanae Andrewes, 1923; Nothoodes longus (Andrewes, 1940), comb. n. of Oodes longus Andrewes, 1940; Nothoodes angustatus (Lorenz, 1998), comb. n. of Oodes angustatus Lorenz, 1998. Lectotypes are designated for Oodes parallelus Motschulsky, 1858, Oodes parallelogrammus Motschulsky, 1858, Oodes desertus Motschulsky, 1858, Oodes cribristernis Bates, 1892, Oodes hahni Reitter, 1908, Oodes thessalonicensis Schatzmayr, 1909, Oodes helopioides var. fiorii Porta, 1923, and Holosoma rambouseki Jedlička, 1931. A key to the species, diagnoses, descriptions, notes on type specimens, relationships, distribution, bionomics when available, and figures of body, genitalia and other characters useful for taxonomy are provided. Numerous new records, including first country records for Romania, Israel, Nepal, China, Thailand, Laos, Vietnam, Brunei, and Indonesia, are registered.
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24

VOLYNKIN, ANTON V., and KAREL ČERNÝ. "Revision of the genus Nephelomilta Hampson, 1900, with descriptions of twelve new species and two new subspecies (Lepidoptera, Erebidae, Arctiinae)." Zootaxa 4472, no. 3 (September 11, 2018): 401. http://dx.doi.org/10.11646/zootaxa.4472.3.1.

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The genus Nephelomilta Hampson, 1900 is revised. The genus Kailasha Singh & Kirti, 2015 is synonymized with Nephelomilta. Twelve new species, N. admiranda, sp. nov. (NE India), N. kanchenjunga, sp. nov. (NE India), N. wolfgangspeideli, sp. nov. (S Vietnam), N. ranau, sp. nov. (Sumatra), N. bana, sp. nov. (C Vietnam), N. martini, sp. nov. (N Vietnam), N. thomaswitti, sp. nov. (Nepal, NE India), N. fangae, sp. nov. (China: Hainan), N. hortensis, sp. nov. (N Thailand), N. melli, sp. nov. (E and S China), N. ferruginea, sp. nov. (Sumatra) and N. diehli, sp. nov. (Sumatra), and two new subspecies, N. sumatrana effractoida, ssp. nov. (N India and Indochina) and N. hortensis fansipana, ssp. nov. (N Vietnam) are described. Barsine fuscobarsine, 2016 is synonymized with Nephelomilta suffusa (Hampson, 1891). Eleven new combinations are established and three taxa previously treated as junior synonyms of N. effracta are upgraded to species level: N. taprobana (Hampson, 1901), comb. nov., N. sumatrana (van Eecke, 1927), comb. & stat. nov., N. gulmargensis (N. Singh, Kirti & D.P. Singh, 2015), comb. nov., N. effracta (Walker, 1854), comb. nov., N. pseudoeffracta (Kirti, Joshi & N. Singh, 2013), comb. nov., N. klapperichi (Daniel, 1952), comb. nov., N. pellucida (Rothschild, 1936), comb. nov., N. babensis (Bae & Bayarsaikhan, 2017), comb. nov., N. karenkonis (Matsumura, 1930), comb. & stat. nov., N. angkorensis (Bayarsaikhan & Bae, 2016), comb. nov., N. pusilla (Wileman, 1910), comb. & stat. nov. Lectotypes for Chionaema effracta sumatrana van Eecke, 1927, Chionaema pellucida Rothschild, 1936 and Chionaema pusilla Wileman, 1910 are designated.
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25

Shokoohy, Mehrdad. "Taprobanê, Ancient Sri Lanka as Known to Greeks and Romans. By D. P. M. Weerakkody, pp. xxii, 287. Turnhout, Brepols, 1997. BEF 2500." Journal of the Royal Asiatic Society 9, no. 1 (April 1999): 170–72. http://dx.doi.org/10.1017/s1356186300016126.

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26

Gildenkov, Mikhail Yurievich. "New data (for 2020) on the distribution of species from the genus Carpelimus Leach, 1819 (Coleoptera: Staphylinidae: Oxytelinae) in the Oriental Region." Samara Journal of Science 10, no. 1 (March 1, 2021): 51–56. http://dx.doi.org/10.17816/snv2021101107.

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New data on the distribution of species from the genus Carpelimus Leach, 1819 in the Oriental Region for 2020 are presented. Carpelimus (s. str.) politus politus (Kiesenwetter, 1850) is recorded for the first time from the Oriental Region, the Jiangxi province in China. Carpelimus (s. str.) raptius Gildenkov, 2019 is recorded for the first time from Vietnam. Carpelimus (s. str.) papuensis (Fauvel, 1879), Carpelimus (Trogophloeus) pseudosimplex Gildenkov, 2013 and Carpelimus (Trogophloeus) simplex (Motschulsky, 1857) are recorded for the first time from Cambodia. Carpelimus (s. str.) praelongus (Bernhauer, 1938) is recorded for the first time from Thailand. Carpelimus (Trogophloeus) plenus Gildenkov, 2019 is recorded for the first time from Malaysia (Borneo) and Indonesia (Sulawesi). Carpelimus (Trogophloeus) geminus Gildenkov, 2018 is recorded for the first time from India, the province of W Bengal. Carpelimus (Trogophloeus) coriaceus (Cameron, 1930) is recorded for the first time from the south of India, the province of Tamil Nadu. Carpelimus (Trogophloeus) magnicollis Gildenkov, 2014, Carpelimus (Trogophloeus) taprobanae (Walker, 1859) and Carpelimus (Trogophloeus) vagans (Cameron, 1930) are recorded for the first time for the central part of India, the province of Madhya Pradesh. Carpelimus (s. str.) communius Gildenkov, 2019 is recorded for the first time from China, the Yunnan province. Carpelimus (s. str.) angusticollis (Bernhauer, 1907), Carpelimus (s. str.) indicus indicus (Kraatz, 1859) and Carpelimus (Troginus) atomus (Saulcy, 1864) are recorded for the first time from the Chinese province of Jiangxi; Carpelimus (Trogophloeus) paripalitans Gildenkov, 2013 is recorded for the first time from the provinces of Jiangxi and Guangdong; Carpelimus (Bucephalinus) formosae (Cameron, 1940) is recorded for the first time from for the province of Hainan. Carpelimus (Troginus) exiguus (Erichson, 1839) is reliably recorded for the Oriental Region from China, the Yunnan province.
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27

"Cotesia taprobanae." CABI Compendium CABI Compendium (January 7, 2022). http://dx.doi.org/10.1079/cabicompendium.15562.

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28

"Stenoptilodes taprobanes." CABI Compendium CABI Compendium (January 7, 2022). http://dx.doi.org/10.1079/cabicompendium.51779.

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29

Pai, Sachin G., C. M. Kalleshwaraswamy, Krishnamoorty Varanashi, M. Ranjith, and M. Rajkumar. "First record of mayfly Povilla (Languidipes) taprobanes Hubbard from Karnataka." Indian Journal of Entomology, August 8, 2022, 1–7. http://dx.doi.org/10.55446/ije.2021.392.

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Mayflies are important as macroinvertebrates of aquatic ecosystems and are reliable bioindicators of water quality. Most mayfly nymphs feed by scraping algae from underwater rocks or by extracting food particles in the littoral and benthic zones of the water bodies. The mayfly Povilla (Languidipes) taprobanes originally described from Sri Lanka was observed in plastic lined ponds in coastal Karnataka. Not only, this is the first report of the species from Karnataka, but the unique case making behaviour of this species is also described for the first time. Additionally, the species was found damaging plastic tarpaulins of 750 gsm thickness used as lining for water storage in the tank by chewing. This chewing behaviour was responsible for damage of plastic sheets leading to water leakage. The possible loss caused and a need of alternate strategies to store water is discussed.
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30

Pederin, Ivan. "Hellenistic travel books and the travel books of greek writers during the roman empire." Radovi. Razdio filoloških znanosti 37, no. 27 (April 18, 2018). http://dx.doi.org/10.15291/radovifilo.1670.

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Es ist wohl kein Zufall, daß der Große Alexander eben diese Länder eroberte, die vor ihm die Reiseschriftsteller beschrieben haben. Die Reisebeschreibungen der Griechen in persischen Diensten und andere, hinter denen wohl Handelsinteressen standen, erfaßten die Welt von Thule bis nach Taprobana und flössen langsam mit der geographischen Wissenschaft zusammen. Afrika, und besonders die Westküste fehlt weitgehend in diesem Weltbild, was wohl eine Folge der Aufteilung der Welt in Einflußsphären ist, wobei die Westküste Afrikas der karthaginischen Interessensphäre zufiel, was anderenorts beschrieben wird. In der griechischen Reisebeschreibung entstand ein Welt-, Geschichts- und Wissenschaftsbild, das erste der westlichen Welt. In dieser Arbeit wurden aber wohl zwei Reisebeschreibungen entdeckt, von denen die Originale verschollen sind und daher sind sie in den Geschichten der griechischenLiteratur nicht enthalten. Beide Reisebeschreibungen konnten nun in leider wortungetreuen Übersetzungen entdeckt werden - es sind die Reisebeschreibungen des Antenor und Pitagora.
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31

Mustika, Adi, Harri Prayogo, and M. Sofwan Anwari. "KEANEKARAGAMAN JENIS SEMUT (Formicidae) DI HUTAN KOTA KABUPATEN KETAPANG KALIMANTAN BARAT." JURNAL HUTAN LESTARI 7, no. 1 (February 6, 2019). http://dx.doi.org/10.26418/jhl.v7i1.31187.

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The diversity of ant species is one of the links in ecosystem stability as decomposing insects as well as food sources so that its existence becomes very ecologically important. Information about the types of ants found in the urban forest of Ketapang Regency is not yet available, therefore the problem of this research is how the diversity of ant species (Formicidae) in the urban forest of Ketapang Regency. This study aims to document the richness and diversity of ant species in the urban forest of Ketapang Regency, West Kalimantan. The method used was purposive sampling and systematic where the placement of traps was carried out according to the presence of ants in terrestrial and arboreal types in secondary forest habitats. Based on the results of research in the urban forest of Ketapang Regency, which was carried out in two types, namely terrestrial type and arboreal type, 10 species of 5 sub-families were found. Sub-families and types of ants found include: Dolichoderinae (Dolichoderus burmanicus, Dolichoderus taprobanae ceramensis), Formicinae (Aphomomyrmex afer, Polirachis browni, Prenolepis fisheri, Chepalotes femoral), Myrmicinae (Crematogester yameni, Crematogester indet), Ponerinae (Odontomachus haematodus), Pseudomyrmecinae (Tetraponera attenuata). The species diversity index (H') in terrestrial type secondary forest habitat (H'= 0.62) and arboreal type (H'= 0.81), the results of the two types in the secondary forest can be concluded that it is still relatively low.Keywords: Ants, Secondary forest habitat, Species diversity
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