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◂Fig. 6 Gynoecial development, fruit and seedling of C. crenata %yellow frames), C. cf. grandicalyx %blue frames) and C. sinensis %pink frames; A–F light microscopy, G–K stereo microscopy of endocarp, mesocarp removed; L–O field images; TS in horizontal orientation). A, B TS of anthetic flower %note two to three abortive ovules and strongly stained, peripheral tissue). C, D TS of anthetic flower %note two to three abortive ovules and lignifying portions of prospective mesocarp). E Young fruit %note developing endocarp and flashily pink portions of the mesocarp). F TS of postanthetic flower %note three abortive ovules and lignifying portions of prospective mesocarp). G TS of endocarp, with three developed embryos removed %note scanty endosperm). H Endocarp. J TS of endocarp. K Endocarp. L Immature fruits. M Mature fruits. N Seedlings %note short hypocotyl and long petioles of cotyledons). O Seedlings %note long hypocotyl and short petioles of cotyledons; image taken from cultivated plant, accession number 2012–0005, in the Botanical Garden Munich) %LS, longisection; TS, transverse section; ao, abortive ovule; cot, cotyledon; db, dorsal bundle; c, calyx; ec, endocarp; ens, endosperm; ex, exocarp; fr, fruit; h, hypocotyl; int, integument; lb, lateral bundle; mc, mesocarp; o, ovule; pet, petiolus; sty, style; ut, peripheral tissue; vs, ventral slit) in Observations on flower and fruit anatomy in dioecious species of Cordia (Cordiaceae, Boraginales) with evolutionary interpretations

◂Fig. 6 Gynoecial development, fruit and seedling of C. crenata %yellow frames), C. cf. grandicalyx %blue frames) and C. sinensis %pink frames; A–F light microscopy, G–K stereo microscopy of endocarp, mesocarp removed; L–O field images; TS in horizontal orientation). A, B TS of anthetic flower %note two to three abortive ovules and strongly stained, peripheral tissue). C, D TS of anthetic flower %note two to three abortive ovules and lignifying portions of prospective mesocarp). E Young fruit %note developing endocarp and flashily pink portions of the mesocarp). F TS of postanthetic flower %note three abortive ovules and lignifying portions of prospective mesocarp). G TS of endocarp, with three developed embryos removed %note scanty endosperm). H Endocarp. J TS of endocarp. K Endocarp. L Immature fruits. M Mature fruits. N Seedlings %note short hypocotyl and long petioles of cotyledons). O Seedlings %note long hypocotyl and short petioles of cotyledons; image taken from cultivated plant, accession number 2012–0005, in the Botanical Garden Munich) %LS, longisection; TS, transverse section; ao, abortive ovule; cot, cotyledon; db, dorsal bundle; c, calyx; ec, endocarp; ens, endosperm; ex, exocarp; fr, fruit; h, hypocotyl; int, integument; lb, lateral bundle; mc, mesocarp; o, ovule; pet, petiolus; sty, style; ut, peripheral tissue; vs, ventral slit)

opencc-by-4.0Aug 2022View details →
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Рис. 1. КоΛичество макрокониΑий грибов роΑа Fusarium (% от общего чисΛа эΛементов морфоΛогии) на органах и в физиоΛогических жиΑкостях картофеΛьной коровки Fig. 1. Number of macroconidia of fungus species from the genus Fusarium (% of the total number of morphological elements) on organs and in physiological fluids of the potato ladybird beetle in On the vector characteristics of the potato ladybird beetle Henosepilachna Vigintioctomaculata (Motsch.) (Coleoptera, Coccinellidae) in the system "phytophagous insect - plant pathogen - plant"

Рис. 1. КоΛичество макрокониΑий грибов роΑа Fusarium (% от общего чисΛа эΛементов морфоΛогии) на органах и в физиоΛогических жиΑкостях картофеΛьной коровки Fig. 1. Number of macroconidia of fungus species from the genus Fusarium (% of the total number of morphological elements) on organs and in physiological fluids of the potato ladybird beetle

opencc-by-4.0Jul 2024View details →
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Рис. 2. ΔоΛговременная Αинамика весенней чисΛенности трех виΑов уток (A — трескунка; B — касатки; C — шиΛохвости) на ΑебеΑинском стационаре Хинганского заповеΑника (показаны уровень значимости и 95-процентный ΑоверитеΛьный интерваΛ) Fig. 2. Long-term spring number dynamics of three duck species at the Lebedinsky Station of Khingansky State Nature Reserve with p-values and 0.95 confidence intervals. A — Gargany; B — Falcated Duck; C — Pintail in The results of long-term observation of waterfowl spring migration in Khingan Nature Reserve, Eastern Russia

Рис. 2. ΔоΛговременная Αинамика весенней чисΛенности трех виΑов уток (A — трескунка; B — касатки; C — шиΛохвости) на ΑебеΑинском стационаре Хинганского заповеΑника (показаны уровень значимости и 95-процентный ΑоверитеΛьный интерваΛ) Fig. 2. Long-term spring number dynamics of three duck species at the Lebedinsky Station of Khingansky State Nature Reserve with p-values and 0.95 confidence intervals. A — Gargany; B — Falcated Duck; C — Pintail

opencc-by-4.0Jul 2024View details →
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Fig. 17 in Extant diversity and estimated number of Gracillariidae (Lepidoptera) species yet to be discovered in the Neotropical region

Fig. 17. Lineage-Through-Time (LTT) plot of Neotropical Gracillariidae. LTT was plotted using 1000 trees from the COI dataset analyses. The number of lineages (y axis) is plotted against time (x axis) in such way that each increase on the number of lineages represents a cladogenesis (a node) in one of the 1000 phylogenetic trees. 2. Dashed red and blue lines represent 95%-confidence intervals for time of starting diversification and LLT plot, respectively.

opencc-by-4.0Jun 2016View details →
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Fig. 16 in Extant diversity and estimated number of Gracillariidae (Lepidoptera) species yet to be discovered in the Neotropical region

Fig. 16. Predictive future cumulative species description curve for the Gracillariidae in the Neotropical region, based on the Logistic model.

opencc-by-4.0Jun 2016View details →
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Fig. 14 in Extant diversity and estimated number of Gracillariidae (Lepidoptera) species yet to be discovered in the Neotropical region

Fig. 14. Variation in number of articles regarding original descriptions on Neotropical gracillariids that were based on adults but that included also data either on gross morphology of immature stages or DNA sequences.

opencc-by-4.0Jun 2016View details →
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Fig. 13 in Extant diversity and estimated number of Gracillariidae (Lepidoptera) species yet to be discovered in the Neotropical region

Fig. 13. Variation in number of type specimens available among museum collections for Neotropical gracillarids. Numbers above bars represent percentages in relation to total number of species (n = 175). See Tab S3 for description of museum acronyms.

opencc-by-4.0Jun 2016View details →
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Fig. 12 in Extant diversity and estimated number of Gracillariidae (Lepidoptera) species yet to be discovered in the Neotropical region

Fig. 12. Relative representation of type specimens for gracillariid species in the Neotropical region. Numbers above bars represent percentages in relation to total number of extant species (n = 175).

opencc-by-4.0Jun 2016View details →
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Fig. 9 in Extant diversity and estimated number of Gracillariidae (Lepidoptera) species yet to be discovered in the Neotropical region

Fig. 9. Diversity of extant gracillariid species (Arabic numbers) in the Neotropics, according to biogeographical regionalization proposed by Morrone (2014). Asterisks indicate areas not contemplated in his restricted definition of the Neotropical region (see text for further description).

opencc-by-4.0Jun 2016View details →
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Figs. 1–8 in Extant diversity and estimated number of Gracillariidae (Lepidoptera) species yet to be discovered in the Neotropical region

Figs. 1–8. Leaf mines (left) and adults (right) from putative species of Neotropical gracillariids: (1, 2) Spinivalva gaucha Moreira & Vargas (Gracillariinae) on Passiflora actinia Hook (Passifloraceae); (3, 4) Porphyrosela minuta Clarke (Lithocolletinae) on Trifolium repens Linnaeus (Fabaceae); (5, 6) Angelabella tecomae Vargas & Parra (Oecophyllembiinae) on Tecoma fulva (Cav.) G. Don (Bignoniaceae); (7, 8) Phyllocnistis sp. (Phyllocnistinae) on Baccharis anomala DC. (Asteraceae). Scale bars = 10, 1, 10, 1, 5, 1, 5, 1 mm, respectively.

opencc-by-4.0Jun 2016View details →
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Fig. 2 in An estimate of the potential number of mayfly species (Ephemeroptera, Insecta) still to be described in Brazil

Fig. 2. Simple linear regression between the number of ephemeropteran species described based on male/female specimens and the year the description was published.

opencc-by-4.0Jul 2015View details →
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Fig. 1 in An estimate of the potential number of mayfly species (Ephemeroptera, Insecta) still to be described in Brazil

Fig. 1. Simple linear regression between the number of ephemeropteran species described based on specimens of the nymphs and/or imagoes and the year the description was published.

opencc-by-4.0Jul 2015View details →
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Figure. The phylogenetic tree showing the relationship among Brevibacillus parabrevis strains SA2.2 and TJ2.3, Bacillus licheniformis MG4.2, and their phylogenetically closest type strains. The GenBank accession numbers of the type strains and studied strains are shown following species names. Distance matrix was calculated by Kimura's 2-parameter model. The scale bar indicates 0.02 substitutions per nucleotide position. Alicyclobacillus pohliae AJ564766 served as an out-group. in Distribution of extracellular enzyme-producing bacteria in the digestive tracts of 4 brackish water fish species

Figure. The phylogenetic tree showing the relationship among Brevibacillus parabrevis strains SA2.2 and TJ2.3, Bacillus licheniformis MG4.2, and their phylogenetically closest type strains. The GenBank accession numbers of the type strains and studied strains are shown following species names. Distance matrix was calculated by Kimura's 2-parameter model. The scale bar indicates 0.02 substitutions per nucleotide position. Alicyclobacillus pohliae AJ564766 served as an out-group.

opencc-by-4.0Dec 2013View details →
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Text-fig. 3. Rhinoppioides quadrituberculatus MIKO gen. et sp. nov. Above: assumed fragments of legs as seen in body cavity of holotype (Aa – in dorsal view, Ab – in ventral view) and paratype (B, only dorsal view available). Below: speculative reconstruction of legs, assumed segments leg IV in above rows (numbers 1, 3, 5, 7, 12, 13, 14), assumed segments of leg I below (numbers 6, 9, 10). Rest of the segments assumed to belong to legs II and III. Only trochanters III (nr. 8) and IV (nr. 7, 12) undoubtedly belonging to the new species. Bars indicating 50 µm, numbers indicate identity of segments. in Oribatid Mite Fossils From Quaternary And Pre-Quaternary Sediments In Slovenian Caves I.Two New Genera And Two New Species Of The Family Oppiidae From The Early Pleistocene

Text-fig. 3. Rhinoppioides quadrituberculatus MIKO gen. et sp. nov. Above: assumed fragments of legs as seen in body cavity of holotype (Aa – in dorsal view, Ab – in ventral view) and paratype (B, only dorsal view available). Below: speculative reconstruction of legs, assumed segments leg IV in above rows (numbers 1, 3, 5, 7, 12, 13, 14), assumed segments of leg I below (numbers 6, 9, 10). Rest of the segments assumed to belong to legs II and III. Only trochanters III (nr. 8) and IV (nr. 7, 12) undoubtedly belonging to the new species. Bars indicating 50 µm, numbers indicate identity of segments.

opencc-by-4.0Jul 2012View details →
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Figure 4 in Review of unique odd chromosome-numbered underground rodent species of the Palearctic region: Ellobius lutescens Thomas 1897 (Rodentia: Cricetidae)

Figure 4. Dorsal (a), ventral (b), and lateral (c) views of cranium and lateral view (d) of mandible of an adult male Ellobius lutescens (Dicle University, Faculty of Science, Department of Biology, Zoology Lab. Mammal collection number 741, from 20 km south of Iğdır, Turkey).

opencc-by-4.0Dec 2015View details →
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Figure 2 in Review of unique odd chromosome-numbered underground rodent species of the Palearctic region: Ellobius lutescens Thomas 1897 (Rodentia: Cricetidae)

Figure 2. Photograph of an adult Ellobius lutescens from Iğdır, Turkey. Photograph by Y Coşkun, collected on 24 April 2013.

opencc-by-4.0Dec 2015View details →
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FIGURE 1 in Paleontologia Electronica is still number one for new open access fossil species

FIGURE 1. Eekaulostomus cuevasae, an extinct armored trumpetfish, and the top open access fossil taxon of 2017 (Farke, 2017). Reproduced from Cantalice and Alvarado-Ortega (2016). 2. Illustration of trumpetfish from Brian Engh, http://dontmesswithdinosaurs.com.

opencc-by-4.0Dec 2017View details →
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Figures 34–37. Homaledra wings. MGCL slide number given. 34 in Two new species of palm-leaf skeletonizers (Lepidoptera: Pterolonchidae: Homaledra Busck)

Figures 34–37. Homaledra wings. MGCL slide number given. 34) H. sabalella (#3321). 35) H. howardi (#3335). 36) H. knudsoni (#5005). 37) H. heptathalama (#5029).

opencc-by-4.0Mar 2021View details →
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Figures 27–33. Homaledra female genitalia, MGCL slide number given. 27 in Two new species of palm-leaf skeletonizers (Lepidoptera: Pterolonchidae: Homaledra Busck)

Figures 27–33. Homaledra female genitalia, MGCL slide number given. 27) H. sabalella (#4566). 28) H. sabalella, detail of signum (#4566). 29) H. sabalella, detail of signum (#3303). 30) H. howardi (#4261). 31) H. howardi, detail of signum (#4261). 32) H. knudsoni (#4673). 33) H. knudsoni, detail of signum (#4673). Scale bars = 500 µm.

opencc-by-4.0Mar 2021View details →
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Fig. 53 in Eggs, Ovariole Numbers, and Modes of Parasitism of Cleptoparasitic Bees, with Emphasis on Neotropical Species (Hymenoptera: Apoidea)

Fig. 53. Eggs of some cleptoparasitic bees from some of my recent publications, all reproduced in the same scale to illustrate the often complex shape of those that are hidden in open cells (above horizontal line) and the simple elongate shapes of those that are introduced into closed cells (below horizontal line). The size difference between the oocytes in these two categories is noteworthy, but is best analyzed in terms of oocyte length compared with body size of the female, i.e., the egg index; see Analyses and Results, subsection Size of Mature Oocytes.

opencc-by-4.0Jul 2003View 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