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Fig. 5 in Three New And Four Newly Recorded Species Of Linyphiinae And Micronetinae Spiders (Araneae: Linyphiidae) From Northern Vietnam
Fig. 5. Nesioneta ellipsoidalis, new species: A, left male palp, retrolateral view; B, ditto, prolateral view; C, ditto, ventral view; D, embolic division, ventral view; E, ditto, dorsal view; F, epigynum, ventral view; G, ditto, dorsal view; H, ditto lateral view; I, vulva, dorsal view. Scale bars = 0.1 mm.
Fig. 4 in Three New And Four Newly Recorded Species Of Linyphiinae And Micronetinae Spiders (Araneae: Linyphiidae) From Northern Vietnam
Fig. 4. Neriene oxycera, new species: A, ocular area of male, dorsal view; B, male left chelicera, frontal view; C, left male palp, retrolateral view; D, ditto, ventral view; E, ditto, prolateral view; F, embolic division, ventral view. Scale bars = 0.1 mm.
Fig. 6 in Three New And Four Newly Recorded Species Of Linyphiinae And Micronetinae Spiders (Araneae: Linyphiidae) From Northern Vietnam
Fig. 6. Nesioneta ellipsoidalis, new species: A, embolus, dorsal view. Nesioneta benoiti (van Helsdingen, 1978): B, embolus, dorsal view; C, embolic division, ventral view; D, ditto, dorsal view. Scale bars: A-B = 0.05 mm; C-D = 0.1 mm.
Fig. 1 in Three New And Four Newly Recorded Species Of Linyphiinae And Micronetinae Spiders (Araneae: Linyphiidae) From Northern Vietnam
Fig. 1. Bathyphantes floralis, new species: A, left chelicera, frontal view; B, left male palp, retrolateral view; C, ditto, prolateral view; D, embolic division, ventral view; E, lamella characteristca, prolateral view; F, embolic membrane, retrolateral view; G, ditto, prolateral view; H, epigynum, ventral view; I, ditto, lateral view; J, vulva, dorsal view. Scale bars = 0.05 mm.
Fig. 2 in Three New And Four Newly Recorded Species Of Linyphiinae And Micronetinae Spiders (Araneae: Linyphiidae) From Northern Vietnam
Fig. 2. Microbathyphantes aokii (Saito, 1982): A, left chelicera, frontal view; B, left male palp, retrolateral view; C, ditto, prolateral view; D, embolic division, ventral view; E, epigynum, ventral view; F, ditto, lateral view; G, vulva, dorsal view. Scale bars = 0.1 mm.
Fig. 8. Parameioneta bilobata Li in Three New And Four Newly Recorded Species Of Linyphiinae And Micronetinae Spiders (Araneae: Linyphiidae) From Northern Vietnam
Fig. 8. Parameioneta bilobata Li & Zhu, 1993: A, embolic division (removing embolus), ventral view; B, embolus, ventral view; C, ditto, ventrolateral view. Scale bars = 0.1 mm.
Fig. 9 in Three New And Four Newly Recorded Species Of Linyphiinae And Micronetinae Spiders (Araneae: Linyphiidae) From Northern Vietnam
Fig. 9. Prosoponoides sinensis (Chen, 1991): A, left chelicera, frontal view; B, left male palp, retrolateral view; C, ditto, ventral view; D, ditto, prolateral view; E, embolic division, ventral view; F, epigynum, ventral view; G, vulva, dorsal view; H, ditto, ventral view. Scale bars = 0.1 mm.
Fig 2. Three dwarf spinner dolphins, Stenella l in Cetacean Diversity And Habitat Preferences In Tropical Waters Of East Kalimantan, Indonesia
Fig 2. Three dwarf spinner dolphins, Stenella l. roseiventris with obscure, lateral color pattern, photographed in the Berau Archipelago, October 2003. Photo: Budiono.
Fig. 4 in Resolution of the identity of three species of Diplostomum (Digenea: Diplostomidae) parasitising freshwater fishes in South Africa, combining molecular and morphological evidence
Fig. 4. Metacercariae of Diplostomum spp. from eye lenses of different fish hosts; (a) Diplostomum sp. from Tilipia sparrmanii, live, ventral view (b) Diplostomum sp. from Tilipia sparrmanii, fixed, ventral view (c) Diplostomum sp. from Tilipia sparrmanii, live, sunken pseudosuckers (arrowhead) (hologenophore, GenBank MN813526, MN813534 and MN808616) (d) Diplostomum sp. 14 sensu Locke et al. (2015) from Synodontis zambezensis, live, ventral view (hologenophore, GenBank MN813541) (e) Diplostomum sp. 14 sensu Locke et al. (2015) from Oreochromis mossambicus, fixed, ventral view, small excretory granules (arrowhead) (hologenophore, GenBank MN813531, MN813539 and MN808621) (f) Diplostomum sp. 14 sensu Locke et al. (2015) from Synodontis zambezensis, fixed, ventral view, large excretory granules (arrowhead) (hologenophore, GenBank MN813541) (g) Diplostomum sp. 16 sensu Locke et al. (2015) from Pseudocrenilabrus philander, fixed, ventral view, everted pseudosuckers (arrowhead) (hologenophore, GenBank MN813532, MN813547 and MN808627) (h) Diplostomum sp. 16 sensu Locke et al. (2015) from Pseudocrenilabrus philander, fixed, ventral view, inverted pseudosuckers (arrowhead) (hologenophore, GenBank MN813533, MN813548 and MN808628) (i) Diplostomum sp. 16 sensu Locke et al. (2015) from Pseudocrenilabrus philander, live metacercariae inside of fish lens. Scale bars: a–h = 100 μm; i = 700 μm.
Fig. 3 in Resolution of the identity of three species of Diplostomum (Digenea: Diplostomidae) parasitising freshwater fishes in South Africa, combining molecular and morphological evidence
Fig. 3. Bayesian inference (BI) and maximum likelihood (ML) phylogram reconstructed using cox1 sequences for species of Diplostomum. Nodal support from BI and ML analyses indicated as BI/ML; only values> 0.90 (BI) and> 70 (ML) are displayed. Scale-bar indicates the expected number of substitution per site. Sequences generated in this study are in bold and indicated by blue rectangles. Codes with isolate information for newly generated sequences are provided in Table 3. Sequences derived from Africa are highlighted in blue, from Asia in purple, from Europe in orange, from North America in green (according to the map) and sequences reported from more than one continent are highlighted in black. Black arrows on the map demonstrate distribution of Diplostomum spathaceum and 'D. mergi Lineage 2' in both, Asia and Europe, and Diplostomum sp. 14 and Diplostomum sp. 16 in both, Africa and Asia. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 2 in Resolution of the identity of three species of Diplostomum (Digenea: Diplostomidae) parasitising freshwater fishes in South Africa, combining molecular and morphological evidence
Fig. 2. Bayesian inference (BI) and maximum likelihood (ML) phylograms reconstructed using (a) partial 28S rDNA sequences (b) ITS1-5.8S-ITS2 sequences for species of Diplostomum. Nodal support from BI and ML analyses indicated as BI/ML; only values> 0.90 (BI) and> 70 (ML) are displayed. Scale-bar indicates the expected number of substitution per site. Sequences generated in this study are in bold and indicated by blue rectangles. Codes with isolate information for newly generated sequences are provided in Table 3. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 1 in Resolution of the identity of three species of Diplostomum (Digenea: Diplostomidae) parasitising freshwater fishes in South Africa, combining molecular and morphological evidence
Fig. 1. Map illustrating the sampling localities on (a) River Riet in Mokala National Park (b) River Phongolo (Site 1, Site 2 and Nyamithi Lake) and the River Usuthu (Shokwe Pan) in Ndumo Game Reserve and (c) River Mooi (Boskop Dam) in Boskop Dam Nature Reserve, South Africa. The illustration was compiled in ArcGIS 10.6 (Available from https://support.esri.com/en/downloads).
Fig. 4 in Natural history notes on three sympatric frogs, Amolops formosus (Günther 1875), Nanorana liebigii (Günther 1860), and Ombrana sikimensis (Jerdon 1870), from Manaslu Conservation Area, Nepal
Fig. 4. Ventral views of live adults: (A) male of Amolops formosus, (B) female of Amolops formosus, (C) male of Nanorana liebigii, and (D) female of Nanorana liebigii. Photos: Biraj Shrestha.
Fig. 6 in Natural history notes on three sympatric frogs, Amolops formosus (Günther 1875), Nanorana liebigii (Günther 1860), and Ombrana sikimensis (Jerdon 1870), from Manaslu Conservation Area, Nepal
Fig. 6. Habitat varieties of the three sympatric frogs: (A) rapidly flowing stream, (B) series of waterfalls inhabited by Amolops formosus, (C) slow flowing shallow stream, and (D) irrigation ditch. Photos: Biraj Shrestha.
Fig. 2 in Natural history notes on three sympatric frogs, Amolops formosus (Günther 1875), Nanorana liebigii (Günther 1860), and Ombrana sikimensis (Jerdon 1870), from Manaslu Conservation Area, Nepal
Fig. 2. Dorsal view of live adults: (A) Ombrana sikimensis, (B) Amolops formosus, and (C) Nanorana liebigii. (D) Dorso-lateral view of Nanorana liebigii. Photos: Biraj Shrestha and Min Bahadur Gurung.
Fig. 5 in Natural history notes on three sympatric frogs, Amolops formosus (Günther 1875), Nanorana liebigii (Günther 1860), and Ombrana sikimensis (Jerdon 1870), from Manaslu Conservation Area, Nepal
Fig. 5. Life stages of Nanorana liebigii: (A) eggs deposition underneath a stone, (B) egg clutch, (C) embryo development, and (D) tadpole with metamorphosed legs. Photos: Biraj Shrestha.
Fig. 4. Chromosomes 9 and 11 from different L. spenceri populations. Three representative chromosomes from each animal demonstrate a in The critically endangered species Litoria spenceri demonstrates subpopulation karyotype diversity
Fig. 4. Chromosomes 9 and 11 from different L. spenceri populations. Three representative chromosomes from each animal demonstrate a highly conserved DAPI negative region in the long arms of chromosome 9. A DAPI negative region is observed in the long arm of chromosome 11, but only in the Central Site juveniles and in only one matched chromosome of the Northern Site x Central Site tadpole hybrid. Arrows indicate the chromosome 11 DAPI negative region. Asterisks indicate the paired submetacentric chromosome 11 matched pair of the Northern Site x Central Site tadpole hybrid.
Figs. 21–25 in Three new species of Lopesia Rübsaamen (Diptera: Cecidomyiidae) from Brazil
Figs. 21–25. Lopesia ubatubensis sp. nov. (21). Third male flagellomere. (22). Third female flagellomere. (23). Twelfh male flagellomere. (24). Tarsal claws and empodia. (25). Male terminalia (dorsal view).
Fig. 12 in Three new species of Lopesia Rübsaamen (Diptera: Cecidomyiidae) from Brazil
Fig. 12. Cylindrical leaf galls of Lopesia mataybae sp. nov. on Matayba guianensis (Sapindaceae). Arrow marks gall.
Figs. 8–11 in Three new species of Lopesia Rübsaamen (Diptera: Cecidomyiidae) from Brazil
Figs. 8–11. Lopesia mataybae sp. nov. (8). Pupal head (ventral view). (9). Prothoracic spiracle. (10). Sixth pupal abdominal tergite (dorsal view). (11). Larval terminal segment (dorsal view).
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.