Find research datasets worth reusing

Fig. 12 in Contribution to the Knowledge of the Genus Atholus (Coleoptera: Histeridae: Histerinae: Histerini) from the Indonesian Archipelago

Fig. 12. Map showing the occurrence of some species of Atholus from the Indonesian archipelago and its extra-limital distribution in the Oriental Region.

Fig. 11 in Contribution to the Knowledge of the Genus Atholus (Coleoptera: Histeridae: Histerinae: Histerini) from the Indonesian Archipelago

Fig. 11. Map showing the occurrence of some species of Atholus from the Indonesian archipelago and its extra-limital distribution in the Oriental Region. A, Atholus coelestis; B, A. philippinesis; C, A. torquatus; D, A. bifrons.

Fig. 10 in Contribution to the Knowledge of the Genus Atholus (Coleoptera: Histeridae: Histerinae: Histerini) from the Indonesian Archipelago

Fig. 10. Atholus singalanus (Marseul, 1880), SEM micrographs, IC-22-in07. A, Elytra, dorsal view; B, ditto, oblique view; C, prosternal process; D, meso- and metaventrite; E, propygidium and pygidium; F, propygidium (punctation); G, protibia, dorsal view; H, ditto, ventral view.

Fig. 9 in Contribution to the Knowledge of the Genus Atholus (Coleoptera: Histeridae: Histerinae: Histerini) from the Indonesian Archipelago

Fig. 9. Atholus singalanus (Marseul, 1880), SEM micrographs, IC-22-in07. A, Habitus, dorsal view; B, ditto, ventral view; C, ditto, oblique view; D, head, dorsal view; E, pronotum; F, mouthparts, ventral view.

Fig. 8 in Contribution to the Knowledge of the Genus Atholus (Coleoptera: Histeridae: Histerinae: Histerini) from the Indonesian Archipelago

Fig. 8. Atholus myrmidon (Marseul, 1861), male genitalia, IC-22-in05. A, Aedeagus, dorsal view; B, ditto, lateral view; C, ninth and tenth tergites, and spiculum gastrale, dorsal view; D, ditto, lateral view; E, eighth tergite and sternite, dorsal view; F, ditto, lateral view. Scale bar: 0.20 mm.

Fig. 6 in Contribution to the Knowledge of the Genus Atholus (Coleoptera: Histeridae: Histerinae: Histerini) from the Indonesian Archipelago

Fig. 6. Atholus myrmidon (Marseul, 1861), SEM micrographs, IC-22-in05. A, Habitus, dorsal view; B, ditto, ventral view; C, ditto, oblique view; D, head, dorsal view; E, pronotum; F, mouthparts, ventral view.

Fig. 7 in Contribution to the Knowledge of the Genus Atholus (Coleoptera: Histeridae: Histerinae: Histerini) from the Indonesian Archipelago

Fig. 7. Atholus myrmidon (Marseul, 1861), SEM micrographs, IC-22-in05. A, Elytra, dorsal view; B, ditto, oblique view; C, prosternal process; D, meso- and metaventrite; E, propygidium and pygidium; F, propygidium (punctation); G, protibia, dorsal view; H, ditto, ventral view.

Fig. 4 in Contribution to the Knowledge of the Genus Atholus (Coleoptera: Histeridae: Histerinae: Histerini) from the Indonesian Archipelago

Fig. 4. Atholus famulus (Lewis, 1892), male genitalia, IC-22-in03. A, Aedeagus, dorsal view; B, ditto, lateral view; C, ninth and tenth tergites, and spiculum gastrale, dorsal view; D, ditto, lateral view; E, eighth tergite and sternite, dorsal view; F, ditto, lateral view. Scale bar: 0.20 mm.

Fig. 2 in Contribution to the Knowledge of the Genus Atholus (Coleoptera: Histeridae: Histerinae: Histerini) from the Indonesian Archipelago

Fig. 2. Atholus famulus (Lewis, 1892), SEM micrographs, IC-22-in03. A, Habitus, dorsal view; B, ditto, ventral view; C, ditto, oblique view; D, head, dorsal view; E, pronotum; F, mouthparts, ventral view.

Fig. 3 in Contribution to the Knowledge of the Genus Atholus (Coleoptera: Histeridae: Histerinae: Histerini) from the Indonesian Archipelago

Fig. 3. Atholus famulus (Lewis, 1892), SEM micrographs, IC-22-in03. A, Elytra, dorsal view; B, ditto, oblique view; C, prosternal process; D, meso- and metaventrite; E, propygidium and pygidium; F, propygidium (punctation); G, protibia, dorsal view; H, ditto, ventral view.

Fig. 1. Some Indonesian Atholus, dorsal habitus. A in Contribution to the Knowledge of the Genus Atholus (Coleoptera: Histeridae: Histerinae: Histerini) from the Indonesian Archipelago

Fig. 1. Some Indonesian Atholus, dorsal habitus. A, Atholus bifrons (Marseul, 1854), IC-22-in01; B, A. philippinensis (Marseul, 1854), IC- 22-in06; C, A. coelestis (Marseul, 1857), IC-22-in02; D, A. myrmidon (Marseul, 1861), IC-22-in05; E, A. famulus (Lewis, 1892), IC-22-in03; F, A. singalanus (Marseul, 1880), IC-22-in07; G, A. torquatus (Marseul, 1854), IC-22-in08. Scale bar: 1.00 mm.

Fig. 5 in Contribution to the Knowledge of the Genus Atholus (Coleoptera: Histeridae: Histerinae: Histerini) from the Indonesian Archipelago

Fig. 5. Atholus famulus (Lewis, 1892), female genitalia, IC-22-in04. A, Dorsal view; B, lateral view; C, gonocoxite, dorsolateral view. Scale bars: 0.20 mm.

opencc-zeroJan 2024View details →

Linked collectors and determiners for: The talitrid amphipod genus Talorchestia from the South China Sea to the Indonesian Archipelago (Crustacea, Senticaudata).

Natural history specimen data linked to collectors and determiners held within, "The talitrid amphipod genus Talorchestia from the South China Sea to the Indonesian Archipelago (Crustacea, Senticaudata)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/4b84979a-e3de-4956-b9c7-91e178dd46b1">https://bionomia.net/dataset/4b84979a-e3de-4956-b9c7-91e178dd46b1</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/4b84979a-e3de-4956-b9c7-91e178dd46b1">https://gbif.org/dataset/4b84979a-e3de-4956-b9c7-91e178dd46b1</a>. Formatted as a Frictionless Data package.

dryad36/100

Phylogenomics of white-eyes, a 'great speciator,' reveals Indonesian archipelago as the center of lineage diversity

Archipelagoes serve as important 'natural laboratories' which facilitate the study of island radiations and contribute to the understanding of evolutionary processes. The white-eye genus Zosterops is a classical example of a 'great speciator', comprising c. 100 species from across the Old World, most of them insular. We achieved an extensive geographic DNA sampling of Zosterops by using historical specimens and recently collected samples. Using over 700 genome-wide loci in conjunction with coalescent species tree methods and gene flow detection approaches, we untangled the reticulated evolutionary history of Zosterops, which comprises three main clades centered in Indo-Africa, Asia, and Australasia, respectively. Genetic introgression between species permeates the Zosteropsphylogeny, regardless of how distantly related species are. Crucially, we identified the Indonesian archipelago, and specifically Borneo, as the major centre of diversity and the only area where all three main clades overlap, attesting to the evolutionary importance of this region.

opencc-zeroDec 2020View details →

zenodo36/100

Risk factors of typhoid infection in the Indonesian archipelago

Datasets and accompanying questionnaires for the epidemiological study on risk factors for typhoid infection conducted between June 2010 and June 2011 from 14 selected hospitals and health centres in three Indonesian islands: in and around Makassar in South Sulawesi (Sulawesi); Jayapura (Papua); Samarinda in East-Kalimantan (Kalimantan). The mansucript describing methods and results has been accepted for publication in PLOS ONE "Risk factors of typhoid infection in the Indonesian archipelago" by Sandra Alba, Mirjam I Bakker, Mochammad Hatta, Pauline FD Scheelbeek, Ressy Dwiyanti , Romi Usman, Andi R Sultan, Muhammad Sabir, Nataniel Tandirogan, Masyhudi Amir, Yadi Yasir,  Rob Pastoor, Stella van Beers,Henk L Smits

opencc-zeroMay 2016View details →

dryad36/100

Phylogenomics of white-eyes, a ‘great speciator,’ reveals Indonesian archipelago as the center of lineage diversity

Open the record for dataset details and reuse information.

publicJan 2021View details →

opennotspecifiedOct 2019View details →

Distribution. Mainland SE Asia, Philippines, Indonesian Archipelago, New Guinea (including Bismarck Archipelago), Solomon Is, and NE Australia; also on N Nicobar Is. in Family Hipposideridae (Old World Leaf-nosed Bats)

Distribution. Mainland SE Asia, Philippines, Indonesian Archipelago, New Guinea (including Bismarck Archipelago), Solomon Is, and NE Australia; also on N Nicobar Is.

opennotspecifiedJan 2009View details →

Subspecies and Distribution. V. t. tangalunga Gray, 1832 — Peninsular Malaysia, Sumatra, Borneo, several Indonesian islands (Amboina I, Banggi I, Langkawi I, Rhio-Lingga Archipelago, Bangka I, Karimata I & Sulawesi), and the Philippines; also two records from Java, but no evidence of native population. V. t. lankavensis Robinson & Kloss, 1920 — Malaysia (Langkawi I). in Viverridae

Subspecies and Distribution. V. t. tangalunga Gray, 1832 — Peninsular Malaysia, Sumatra, Borneo, several Indonesian islands (Amboina I, Banggi I, Langkawi I, Rhio-Lingga Archipelago, Bangka I, Karimata I & Sulawesi), and the Philippines; also two records from Java, but no evidence of native population. V. t. lankavensis Robinson & Kloss, 1920 — Malaysia (Langkawi I).

opennotspecifiedAug 2011View details →

Distribution. Sulawesi and adjacent Is (Buton, Kabaena, Muna, Peleng, Lembeh, and on some of the Togian Is); thought to be extinct on Selayar I. Pigs have been widely domesticated through the Indonesian archipelago and beyond. This primarily involved the Eurasian Wild Pig (S. scrofa), but also S. celebensis, the only other species of pig successfully domesticated. Mitochondrial DNA studies of the dispersion of these domesticated forms agree on three major dispersal events, two involving S. scrofa and one S. celebensis. Evidence supports an early human-mediated translocation of S. celebensis to Flores and Timor and two later, separate human-mediated dispersals of domestic pig through islands of SE Asia into Oceania. In addition to Flores and Timor, S. celebensis is also thought to occur in its domesticated form on Halmahera, Lendu, Roti, and Savur Is, and even on Simeulue and Nias Is to the W of Sumatra and far from its island of origin, Sulawesi. In the Moluccas, and possibly elsewhere in this region, introduced S. celebensis are thought to have hybridized with other introduced pigs of S. scrofa derivation, and apparent hybrids between these species are now reported to survive on a number of islands, including Salawatti, Great Kei, Dobu, Seram, Ambon, Bacan, Ternate, Morotai, and New Guinea. It is also reported that in the 19" century the sows of domestic pigs in Sulawesi frequently mated with wild animals, after which they returned to their villages. in Suidae

Distribution. Sulawesi and adjacent Is (Buton, Kabaena, Muna, Peleng, Lembeh, and on some of the Togian Is); thought to be extinct on Selayar I. Pigs have been widely domesticated through the Indonesian archipelago and beyond. This primarily involved the Eurasian Wild Pig (S. scrofa), but also S. celebensis, the only other species of pig successfully domesticated. Mitochondrial DNA studies of the dispersion of these domesticated forms agree on three major dispersal events, two involving S. scrofa and one S. celebensis. Evidence supports an early human-mediated translocation of S. celebensis to Flores and Timor and two later, separate human-mediated dispersals of domestic pig through islands of SE Asia into Oceania. In addition to Flores and Timor, S. celebensis is also thought to occur in its domesticated form on Halmahera, Lendu, Roti, and Savur Is, and even on Simeulue and Nias Is to the W of Sumatra and far from its island of origin, Sulawesi. In the Moluccas, and possibly elsewhere in this region, introduced S. celebensis are thought to have hybridized with other introduced pigs of S. scrofa derivation, and apparent hybrids between these species are now reported to survive on a number of islands, including Salawatti, Great Kei, Dobu, Seram, Ambon, Bacan, Ternate, Morotai, and New Guinea. It is also reported that in the 19" century the sows of domestic pigs in Sulawesi frequently mated with wild animals, after which they returned to their villages.