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Fig. 6 in A revision of the South American species of the cleptoparasitic bee genus Triepeolus Robertson, 1901 (Hymenoptera: Apidae)

Fig. 6. Triepeolus buchwaldi (Friese, 1908). A. Female (AMNH M.G.R. Database No. 1328), habitus, lateral view. B, D. Female (AMNH M.G.R. Database No. 3707). B. Habitus, dorsal view. C. Male (INHS 387483), habitus, lateral view. D. Pseudopygidial area, dorsal view.

opencc-by-4.0Apr 2024View details →
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Figure 6. Rosa cieselskii B in Rosa Cieselskii Bÿocki Or Rosa × Subcollina (Christ) Dalla Torre & Sarnth. - Which Species Does Occur In Latvia?

Figure 6. Rosa cieselskii B˘ocki from KW herbarium. Label: Ternopol region (W Ukraine), Zalischiki village, steep slope by the river Dnister, voucher no. KW001003162.

opencc-by-4.0Dec 2023View details →
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Figure 6 in Ecological Features And Anthropogenic Transformation Of Wetlands As Part Of Urban Floras Of Ukraine

Figure 6. Proportion of number of native and adventive plant species in wetland flora in studied territories.

opencc-by-4.0Aug 2023View details →
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Fig. 6 in Taxonomic notes on some Cantharidae of Sicily and North Africa

Fig. 6. Metacantharis puncticollis (Levrat, 1857). Neotypus preserved in the Walter Wittmer collection at the Natural History Museum of Basel.

opencc-by-4.0Dec 2020View details →
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Fig. 6 in Fossil soldier beetles of the Anders Damgaard amber collection. Fourth update

Fig. 6. Podistra (Absidia) mattheseni sp. nov. ALDC0566/ALD.Ba.Can.27 in Baltic amber. A: Holotype, detail of head and pronotum, bar = 0.5 mm; B: Holotype, detail of head and palps (lateral view), bar = 0.3 mm; C: Holotype, detail of left antenna, bar = 0.5 mm; D: Holotype, detail of tarsomeres and last tergite, bar = 0.2 mm.

opencc-by-4.0Dec 2020View details →
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Figure 6 in Seasonal analysis of Saturniidae (Insecta: Lepidoptera: Bombycoidea) in a remaining Atlantic Forest in the State of Espírito Santo, Brazil

Figure 6. Arsenurinae subfamily found in the Vale Nature Reserve, Linhares, EspÍrito Santo, Brasil. Scale: 2 cm. / Subfamilia Arsenurinae encontrado en la Reserva Natural Vale, Linhares, EspÍrito Santo, Brasil. A) Arsenura armida (Cramer, 1779). B) Arsenura ponderosa ponderosa Rothschild, 1895. C) Arsenura sylla (Walker, 1855). D) Copiopteryx semiramis phoenix (Deyrolle, 1869). E) Loxolomia serpentina Maassen, 1869. F) Paradaemonis pluto (Westwood, 1854). Escala: 2 cm.

opencc-by-4.0Feb 2022View details →
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Fig. 6 in Effects of urbanization on the diversity of testate amoebae (Protist, Rhizopoda) in a stream of the southwestern Amazon basin (Igarapé São Francisco in Acre state, Brazil)

Fig. 6. Biplot of the first two axes of the Redundancy Analysis of the scores of the streams according to the abiotic variables (TC = Thermotolerant Coliforms; EC = Electrical Conductivity, DO = Oxygen; pH = Hydrogen potential; TotP = Total Phosphorus; Temp = Temperature; Turb = Turbidity; NH 4 = Ammonia; NO 2 = Nitrate), the legend explains the symbols corresponding to the family names.

opencc-by-4.0Dec 2023View details →
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Fig. 6 in Certesella larai (Amoebozoa: Arcellinida: Hyalospheniformes) a new soil testate amoeba species from the Dominican Republic and Chile challenges the definition of genera Certesella and Porosia

Fig. 6. Comparative overview of the morphology of all known species of genera Certesella and Porosia species. A: Certesella larai n. sp., B: C. certesi, C: C. australis, D: C. murrayi, E: C. martiali, F: Porosia paracarinata, G: P. bigibbbosa. Images are not to scale as some early images lacked a scale.

opencc-by-4.0Feb 2022View details →
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Fig. 6 in Spirostomum teres: A Long Term Study of an Anoxic-Hypolimnion Population Feeding upon Photosynthesizing Microorganisms

Fig. 6. Spirostomum teres: a) Lake Alchichica (8/8/2011, 30 m), b) Lake La Preciosa (2/9/2011, 20.5 m and c) Lake de La Cruz (25/6/2010, 11.25 m. Protargol stain (QPS). 1 ≡ 10 µm.

opencc-by-4.0Dec 2020View details →
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Fig. 6 in Immunocytochemical Analysis of α-Tubulin Distribution Before and After Rapid Axopodial Contraction in the Centrohelid Raphidocystis contractilis

Fig. 6. Confocal analysis of α-tubulin-immunolabeled extended axopodia. Fine reconstructed projection image from 161 optical sections taken at a 0.05 µm (top) and the corresponding light micrograph (bottom). Note the regions of relatively low fluorescence (arrowheads) did not correspond to the location of kinetocysts (arrows). Scale bar: 10 μm.

opencc-by-4.0Dec 2020View details →
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Fig. 6 in A Study on Resting Cysts of an Oxytrichid Soil Ciliate, Rigidohymena quadrinucleata (Dragesco and Njine, 1971) Berger, 2011 (Ciliophora, Hypotrichia), Including Notes on its Encystation and Excystation Process

Fig. 6. Rigidohymena quadrinucleata, the basic scheme of two excystation modes. The standard mode: The beginning of excystation process is connected with formation of a transparent space between cyst wall and excysting cell. A little later, appears the excystation vacuole. The regenerating specimen breaks the cyst wall and escapes within the single, transparent membrane. The transparent membrane is broken by the excystant and resorbed in the enviroment. The rare mode: The beginning of excystation is associated, similarly, as in the standard mode, with formation of a transparent space and excystation vacuole. The regenerating specimen breaks the transparent membrane first, instead of breaking the whole cyst wall. Finally, the rest of the cyst wall is ruptured by the moving cell and the pressure of the excystation vacuole. The cell leaves the resting cyst. The transparent membrane remains in the empty cyst as a residual body.

opencc-by-4.0Dec 2017View details →
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Fig. 6 in Morpho-molecular Characterization of the Litostomatean Predatory Ciliate Phialina pupula (Müller, 1773) Foissner, 1983 (Haptoria, Lacrymariidae)

Fig. 6. Phylogeny based on the 18S rRNA gene of 22 taxa from the family Lacrymariidae (18S-lac1 alignment). Note that the genus Phialina is paraphyletic and contains the polyphyletic genus Lacrymaria. Posterior probabilities for the Bayesian inference and bootstrap values for maximum likelihood were mapped onto the 50%-majority rule ML tree. Sequences in bold were obtained during this study. The scale bar indicates nine substitutions per one thousand nucleotide positions.

opencc-by-4.0Dec 2019View details →
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Fig. 6 in Exploring the diversity and ecology of testate amoebae in West Siberian peatlands

Fig. 6. Plots of taxon abundance versus moisture content for the twelve most abundant testate amoeba taxa. All taxa show a significant correlation with moisture (Spearman Rs, P <0.05) with the exception of Nebela tincta.

opencc-by-4.0Dec 2017View details →
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FIGURE 6 in A new species of Moenkhausia (Characiformes: Characidae) from the rio Madeira basin, Brazil, with comments on the evolution and development of the trunk lateral line system in characids

FIGURE 6 | Distribution of Moenkhausia cambacica in the upper rio Machado, rio Madeira basin, Brazil. Black star (type-locality), blue star (other localities).

opencc-by-4.0Jun 2021View details →
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Fig 6 in The last giants: New evidence for giant Late Triassic (Rhaetian) ichthyosaurs from the UK

Fig 6. Histological overview of BRSMG Cg3178 (BAS surangular). A. Composite image of thin section under circular polarized light. B. Close-up of the external margin of the outer cortex, showing the presence of multiple growth marks (GMs), open vascular canals and cortical vascular canals with all degrees of maturity (simple canals, primary osteons and secondary osteons), supporting an ongoing active and continuous growth. Note the evident darker border of the lumen of a diagonal canal running from the top left toward the margin of the large nutrient canal (NC) showing further longitudinal vascularization. C. Concentric secondary osteon in the outer cortex under lambda filter. D. Close-up of the upper margin of the nutrient canal under crossed polarized (left) and circular polarized light (right). The growth marks appear as alternated tightly packed rows of brighter and darker periosteal intrinsic fibres (PIF). The same tight packing of the GMs occurs also deeper in the cortex. E. Lateral margin of the nutrient canal under circular polarized view. PIF are evident as bright yellow and blue coiled structures. The presence of simple canals alongside osteons, indicates primary deposition of bone along the margin of the large nutrient canal. F. Concentric secondary osteon in the trabecular bone under transmitted light. It is evident the high amount of osteocyte lacunae and the presence of plump irregular shaped ones in the lamellar bone. G. Trabecular bone under circular polarized view. The presence of primary matrix and concentric secondary osteons indicate that the trabeculae are secondary, produced from compact bone made cancellous. White arrows (D, E, G) point at PIF; white arrowheads point at resorption lines in concentric osteons (C, F, G); white dotted lines indicate borders of primary osteons (C, F, G); yellow arrow heads (B, D) point at rows of GMs. Abbreviations. LB, Lamellar bone; NC, Nutrient canal; OC, Open periosteal canal; PO, Primary osteon; RC, Resorption cavity; SC, Simple canal; SO, Secondary osteon. https://doi.org/10.1371/journal.pone.0300289.g006

opencc-by-4.0Apr 2024View details →
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Figure 6 in Microstonyx (Suidae, Artiodactyla) from the Upper Miocene of Hayranlı-Haliminhanı, Turkey

Figure 6. Bivariate plots of the upper cheek teeth: length (DAP) versus width of the anterior (DTa) or posterior lobes (DTp). Legend for the lower and upper cheek teeth (Figures 2–4): Hippopotamodon sivalense from the Siwaliks (IM, GSP, NHI, UL, NMB, BSP, FISF); Hippopotamodon antiquus from Bayraktepe (MTA), Eppelsheim (HLD), Esme Akçaköy (PIMUZ), Kayincak (UA), Montrigaud (MLG), Middle Sinap (MTA, MNHN), St. Jeande-Bournai (NMB), Usak (MTA); Microstonyx major from Allisas (MGL), Baltavár (HGSB, NMW), Basaleti (GSM), Bayir (MTA), Bayramkalesi (UA), Çeltek Küyü (MTA), Chalon (UCBL), Çobanpınar (MTA, UA), Concud (NHM), Concud - Barranco de las Calaveras (IVAU), Concud - Cerro de la Garita (MNCN, IVAU, IPS, MPZ, Collection Pepe Orrios, Teruel), Çorak Yerler (UA, PIMUZ), Crevillente 2 (MHMN, MPV), Crevillente 15 (MHMN), Csákvár (HGSB), Cucuron or Vaugines (MRA), Das (MLGSB), Eldar (GSM), Evciköy (MTA), Garkin (MTA), Grebeniki (VMM), Gökdere (UA), Elmadağ (UA), Gülpınar (MTA), Igbek (= Sinap loc. 49; SP), Kayadibi (MTA, PIMUZ), Kohfiddisch (NMW), Küçük Yozgat (UA), Lapsehi-Subasi (MTA), Luzinay (MGL), Mahmutgazi (MTA), Montredon/Mont Léberon (UCBL, MGL), Paşabağı (UA), Piera (IPS, MLGSB, MGB), Polgárdi (HGSB, NMB), Puente Minero (CPO), Salihpaşalar (MTA), Salmendingen (NMB), Schernham (NMW), Sehlek (MTA), Sinap loc. 26 (SP), Sivas-Hayranlı (MTA), Sivas loc. 2 (UA), Sivas loc. 19 (UA), Siwaliks (IM, cast IGF), Stratzing (NMW, KME), Taraklia (PIN), Terrassa (IPS), Tersanne (UCBL), Titov Veles (IVAU), La Tour du Pin (MGL), Udabno (GSM), Várpalota (HGSB), Vaugines (MRA); Microstonyx erymanthius from Ano Metochi 4 (IVAU), Dorn Dürkheim (FISF), Kavakdere (= Sinap loc. 33; MTA, PIMUZ, SP), Kerasia (IVAU), Maragha (NMW, MTA, IVAU), Maragha - Kopran (NMW), Pikermi (NHM, IPUW MGL, MSNO, TMH, MGPUSB), Pikermi - Chomateri (NMW), Samos (NMW, HLD, NMB, NMBe), Soblay (UCBL, MGL).

opencc-by-4.0Dec 2012View details →
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Fig. 6 in New genera of stiletto flies endemic to Madagascar (Therevidae: Therevinae)

Fig. 6. Rinhatiana distincta (Lyneborg, 1976) comb. nov., ♀, (CSCA). A. Lateral view. B. Oblique view.

opencc-by-4.0Apr 2024View details →
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Figure 6 in Updates on the classification and numbers of marine fungi

Figure 6: Phylogram generated from maximum likelihood (ML) analysis based on combined LSU, ITS, and act1 sequence data representing Sarocladiaceae (Hypocreales). Thirty-seven strains are included in the combined analyses which comprised 1753 characters (504 characters for LSU, 478 characters for ITS, 771 characters for act1) after alignment. Acremonium variecolor strains CBS 130360 and FMR 11141 in Bionectriaceae (Hypocreales) were used as the outgroup taxa. The best scoring RAxML tree with a final likelihood value of −8526.836 is presented. The matrix had 435 distinct alignment patterns, 356 parsimony-informative, 73 singleton sites, and 1332 constant sites. Estimated base frequencies were as follows: A = 0.216, C = 0.298, G = 0.265, T = 0.221; substitution rates: AC = 2.09479, AG = 3.08268, AT = 2.09479, CG = 1.00000, CT = 10.05849, GT = 1.000000; gamma distribution shape parameter α = 0.574. Bootstrap support values for ML equal to or greater than 75 % are given above the nodes (left side). Bayesian posterior probabilities (BYPP) equal to or greater than 0.95 are given above the nodes (right side). Ex-type strains are in bold and newly generated sequences are in blue.

opencc-by-4.0Jul 2023View details →
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Figure 6 in Looks can be deceiving: contrasting temperature characteristics of two morphologically similar kelp species co-occurring in the Arctic

Figure 6: Sex ratio (female:male) of gametophytes of Laminaria digitata (left) and Hedophyllum nigripes (right) after 14 days in temperature gradients between 0 and 25 °C (L. digitata) and 22 °C (H. nigripes) (n = 4, mean ± SD). Different letters denote significant differences among temperatures within each species (L. digitata: Kruskal–Wallis test with multiple p-value comparison; H. nigripes: one-way ANOVA with Tukey's post hoc test). Please note that the marked deviation from an expected initial 50:50 ratio was due to applied seeding methods. †All gametophytes died.

opencc-by-4.0May 2021View details →
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Figures 4–6 in DNA sequencing reveals three new species of Chamberlainium (Corallinales, Rhodophyta) from South Africa, all formerly passing under Spongites yendoi

Figures 4–6: Habit photographs of Chamberlainium capense, C. glebosum and C. occidentale. (4) Chamberlainium capense is moderately thick to mostly lumpy and only slightly protuberant. Scale bar = 20 mm. (5) Chamberlainium glebosum is thick, very lumpy and highly protuberant. Scale bar = 20 mm. (6) Chamberlainium occidentale is morphologically highly variable, occurring as thin encrusting (smooth) to thick warty (mostly) to lumpy plants, and are only slightly protuberant. Scale bar = 30 mm.

opencc-by-4.0Jan 2021View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

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