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Figure 5 in Integrated morphological, CO1 and distributional analysis confirms many species in the Iridomyrmex anceps (Roger) complex of ants
Figure 5. Distribution records of sequenced specimens from the Iridomyrmex anceps complex in Australia. Monsoonal tropics region shaded in grey. A. Species A, G, H and I. B. Species B, J, K, L, M, N, O and R. Abbreviations: WA—Western Australia, NT— Northern Territory, Qld—Queensland.
Figure 3 in Integrated morphological, CO1 and distributional analysis confirms many species in the Iridomyrmex anceps (Roger) complex of ants
Figure 3. Scape length in relation to head length for selected species. A. Species A, G, H, I and J. B. Species B, K, L, M and N.
Figure 2 in Integrated morphological, CO1 and distributional analysis confirms many species in the Iridomyrmex anceps (Roger) complex of ants
Figure 2. Summary CO1 tree of the 82 sequenced specimens of Iridomyrmex anceps. Maximum-likelihood phylogeny inferred using IQ-TREE. Black and red circles indicate bootstrap support values ≥90 and ≥70, respectively. The full CO1 tree is shown in Supplementary Figure 1. Abbreviations: WA—Western Australia, NT—Northern Territory, Qld—Queensland, PNG—Papua New Guinea.
Figure 1 in Integrated morphological, CO1 and distributional analysis confirms many species in the Iridomyrmex anceps (Roger) complex of ants
Figure 1. Head (A) and lateral (B) views of a typical member of the Iridomyrmex anceps complex (sp. A; specimen IRIDO217-16). Scale bars = 1 mm.
Fig. 3 in Extended distribution patterns of the Arabian burnet moth Reissita simonyi (R , 1899) (Lepidoptera: Zygaenidae) and the Arabian wall brown Lasiommata felix (W , 1929) (Lepidoptera: Nymphalidae: Satyrinae) in Southern Arabia
Fig. 3: A typical place to find Lasiommata felix near Bani Mawhab / Bait Muzaret. The artificial walls seem to be a suitable habitat for L. felix.
Fig. 4 in Extended distribution patterns of the Arabian burnet moth Reissita simonyi (R , 1899) (Lepidoptera: Zygaenidae) and the Arabian wall brown Lasiommata felix (W , 1929) (Lepidoptera: Nymphalidae: Satyrinae) in Southern Arabia
Fig. 4: Distribution of Reissita simonyi yemenicola (along the Red Sea) and Reissita simonyi simonyi (along the Indian Ocean at both sides of the Yemeni-Omani border).
Fig. 14. Distribution map. 1 in New species and new records of terrestrial isopods (Crustacea, Isopoda, Oniscidea) of the families Philosciidae and Scleropactidae from Brazilian caves
Fig. 14. Distribution map. 1. Alboscia jotajota Campos-Filho, Bichuette & Taiti sp. nov. 2. Androdeloscia akuanduba Campos-Filho, Cardoso & Taiti sp nov. 3. Atlantoscia inflata Campos-Filho & Araujo, 2015. 4. Benthana iporangensis Lima & Serejo, 1993. 5. B. longicornis Verhoeff, 1941. 6. B. olfersii (Brandt, 1833). 7. B. picta (Brandt, 1833). 8. B. taeniata Araujo & Buckup, 1994. 9. Metaprosekia igatuensis Campos-Filho, Fernandes & Bichuette sp. nov. 10. Paratlantoscia rubromarginata (Araujo & Leistikow, 1999). 11. Amazoniscus spica Campos-Filho, Aguiar & Taiti sp. nov. 12. Circoniscus bezzii Arcangeli, 1931. Light gray areas denote Brazilian conservation units. AL = Alagoas; BA = Bahia; CE = Ceará; DF = Distrito Federal; ES = Espírito Santo; GO = Goiás; MA = Maranhão; MG = Minas Gerais; MT = Mato Grosso; PA = Pará; PB = Paraíba; PE = Pernambuco; PI = Piauí; PR = Paraná; RJ = Rio de Janeiro; RN = Rio Grande do Norte; SE = Sergipe; SP = São Paulo; TO = Tocantins.
Figure 2 in Forest monkeys and Pleistocene refugia: a phylogeographic window onto the disjunct distribution of the Chlorocebus lhoesti species group
Figure 2. All possible patterns of relationships among the lhoesti group species. A, topology consistent with a vicariant scenario in which the distribution of a widespread common ancestor fragments into three segments – nearly simultaneously – as the result of habitat deterioration associated with a Pleistocene glacial cycle. B, topology consistent with an alternative vicariant scenario, in which ancestral populations of Chlorocebus preussi and Chlorocebus solatus remain in contact for a short time after the divergence of Chlorocebus lhoesti, because the former two stocks range within the same Pleistocene refuge. C, tree consistent with a dispersal hypothesis in which early C. preussi populations (following divergence from C. solatus) migrate along the northern rim of the Congo Basin, and found a new lineage (C. lhoesti) in the Albertine region (see Fig. 1). D, tree consistent with a dispersal hypothesis in which early C. solatus populations (following divergence from C. preussi) conduct a similar transcontinental migration, but along the southern rim of the Congo Basin (see Fig. 1).
Fig. 2 in Species Diversity And Distribution Of Synanthropic Acarid Mites (Acariformes, Acaridia) In Transcarpathia
Fig. 2. Species diversity and the number of acarid mites in farm buildings in different zones of Transcarpathia.
Fig. 6 in Phenotypic Study Of Population And Distribution Of The Poecilia Reticulata (Cyprinodontiformes, Poeciliidae) From Kyiv Sewage System (Ukraine)
Fig. 6. Dependence of the area of orange spots (stripes, %) on the body length of male guppies (L) P. reticulata.
Fig. 1 in Phenotypic Study Of Population And Distribution Of The Poecilia Reticulata (Cyprinodontiformes, Poeciliidae) From Kyiv Sewage System (Ukraine)
Fig. 1. Potential (probabilistic) model of P. reticulata current world expansion built in the Maxent program based on the CliMond climatic data and GBIF data (2021). Areas of highest habitat suitability (> 0.5) are colored in red and areas of lowest (<0.1) — in blue.
Fig. 7 in Phenotypic Study Of Population And Distribution Of The Poecilia Reticulata (Cyprinodontiformes, Poeciliidae) From Kyiv Sewage System (Ukraine)
Fig. 7. Dependence of the proportions of the tail (C1/C2) on the body length of P. reticulata: C1/C2 = 1 ("symmetrical tail") is shown by the line.
Fig. 1 in Species Diversity And Distribution Of Synanthropic Acarid Mites (Acariformes, Acaridia) In Transcarpathia
Fig. 1. Map of acarid mites collection sites in Transcarpathian Region: a — map of Transcarpathian Region by altitudinal zonation; b — air temperature map of Transcarpathian Region; c — precipitation map of Transcarpathian Region.
Figure 13 in Taxonomy of Oncaeidae (Copepoda, Poecilostomatoida) from the Red Sea. V. Three species of Spinoncaea gen. nov. (ivlevi-group), with notes on zoogeographical distribution
Figure 13. Spinoncaea tenuis sp. nov., female (Red Sea). (A) Antenna; (B) labrum, anterior; (C) same, posterior; (D) mandible, showing individual elements; (E) maxillule; (F) maxilla; (G) maxilliped, anterior; (H) paragnaths, ventral.
Figure 6 in Taxonomy of Oncaeidae (Copepoda, Poecilostomatoida) from the Red Sea. V. Three species of Spinoncaea gen. nov. (ivlevi-group), with notes on zoogeographical distribution
Figure 6. Spinoncaea ivlevi (Shmeleva, 1966) comb. nov., female, elongate form (Red Sea). (A) Habitus, dorsal; (B) urosome, dorsal, seta V on CR omitted [b: P5-bearing somite, ventral, showing midventral spinous processes, exopodal setae omitted]; (C) P4, endopod, anterior, showing reduced inner setae on second segment. Spinoncaea ivlevi (Shmeleva, 1966) comb. nov., female (Adriatic Sea). (D) Habitus, dorsal, pore pattern on prosome not fully discerned; (E) urosome, dorsal; (F) caudal ramus, dorsal, seta VII shown separately; (G) P4, endopod, posterior.
Figure 9 in Taxonomy of Oncaeidae (Copepoda, Poecilostomatoida) from the Red Sea. V. Three species of Spinoncaea gen. nov. (ivlevi-group), with notes on zoogeographical distribution
Figure 9. Spinoncaea humesi sp. nov., female (Red Sea). (A) Antenna; (B) labrum, anterior; (C) same, posterior; (D) mandible, showing individual elements; (E) maxillule; (F) maxilla; (G) maxilliped, anterior.
Figure 4 in Taxonomy of Oncaeidae (Copepoda, Poecilostomatoida) from the Red Sea. V. Three species of Spinoncaea gen. nov. (ivlevi-group), with notes on zoogeographical distribution
Figure 4. Spinoncaea ivlevi (Shmeleva, 1966) comb. nov., female, robust form (Red Sea). (A) P1, anterior [a: second endopod segment, arrow indicating ornamentation on inner margin]; (B) P2, anterior, intercoxal sclerite not shown; (C) P3, posterior; (D) P4, anterior, intercoxal sclerite not shown.
Figure 3 in Taxonomy of Oncaeidae (Copepoda, Poecilostomatoida) from the Red Sea. V. Three species of Spinoncaea gen. nov. (ivlevi-group), with notes on zoogeographical distribution
Figure 3. Spinoncaea ivlevi (Shmeleva, 1966) comb. nov., female, robust form (Red Sea). (A) Antenna, lateral elements are numbered using Roman numerals, distal elements are identified by capital letters; (B) labrum, anterior; (C) same, posterior; (D) mandible, showing individual elements, which are identified by capital letters; (E) maxillule; (F) maxilla; (G) maxilliped, anterior.
Figure 1 in Taxonomy of Oncaeidae (Copepoda, Poecilostomatoida) from the Red Sea. V. Three species of Spinoncaea gen. nov. (ivlevi-group), with notes on zoogeographical distribution
Figure 1. Location of stations. ' = VALDIVIA-Cruise 29, October 1980; - = METEOR-Cruise 5/1, January 1987; • = METEOR-Cruise 5/3b, May 1987; ' = METEOR-Cruise 5/5, July/August 1987; · = METEOR-Cruise 44/2, March 1999.
Figure 5 in Taxonomy of Oncaeidae (Copepoda, Poecilostomatoida) from the Red Sea. V. Three species of Spinoncaea gen. nov. (ivlevi-group), with notes on zoogeographical distribution
Figure 5. Spinoncaea ivlevi (Shmeleva, 1966) comb. nov., male (Red Sea). (A) Habitus, dorsal; (B) maxilliped, anterior [b: same, medial view, claw partly omitted]; (C) maxilliped, posterior; (D) urosome, dorsal, seta V on CR omitted; (E) urosome, ventral; (F) same, lateral; (G) antennule, small middle aesthetasc close to seta figured separately.
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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.