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Fig. 1 in Phylogenetic relationships within the flatworm genus Matuxia (Platyhelminthes, Tricladida, Continenticola) inferred from molecular data with the description of a southern lineage of the genus

Fig. 1 Distributional range of the genus Matuxia in areas of Atlantic Forest from southeastern and southern Brazil

opennotspecifiedAug 2019View details →
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Fig. 3 in Phylogenetic relationships within the flatworm genus Matuxia (Platyhelminthes, Tricladida, Continenticola) inferred from molecular data with the description of a southern lineage of the genus

Fig. 3 Matuxia tymbyra Rossi & Leal-Zanchet, sp. nov.: a–b photograph of live specimens, a MZU PL.00181 and b holotype, in dorsal view; c colour pattern of the holotype after fixation in dorsal view; d eye pattern of a fixed specimen (MZU PL.00183) in dorsal view. Anterior tip to the left. The position of the pharynx and copulatory apparatus is indicated by the light marks on dorsal surface in c

opennotspecifiedAug 2019View details →
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Fig. 4 in A widespread commensal loses its identity: suggested taxonomic revision for Indotyphlops braminus (Scolecophidia: Typhlopidae) based on molecular data

Fig. 4 The distributions of the three putative species, plotted on an annual precipitation layer (BIOCLIM 12) to indicate the wet zone

opennotspecifiedAug 2022View details →
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Fig. 3 in A widespread commensal loses its identity: suggested taxonomic revision for Indotyphlops braminus (Scolecophidia: Typhlopidae) based on molecular data

Fig. 3 Lateral view of the head of specimens. a CES17213 (wet zone I. braminus), b CES151013 (dry zone I. braminus), c CES16711 (I. pammeces). R= rostral, PN = pre-nasal, NA = nasal, PO = pre-ocular, SL 1–4 = Supralabial scales 1–4

opennotspecifiedAug 2022View details →
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Fig. 9 in A widespread commensal loses its identity: suggested taxonomic revision for Indotyphlops braminus (Scolecophidia: Typhlopidae) based on molecular data

Fig. 9 Coalescent species tree built using seven nuclear markers (AMEL, BDNF, CMOS, CAND1, NT3, RAG1, and ZEB2) in *BEAST. The nodes with posterior probability≥ 0.8 are indicated with a solid black circle

opennotspecifiedAug 2022View details →
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Fig. 6 in A widespread commensal loses its identity: suggested taxonomic revision for Indotyphlops braminus (Scolecophidia: Typhlopidae) based on molecular data

Fig. 6 Bayesian assignment of the 25 individuals to three populations based on the, using STRUCTURE. The individual ids are indicated below each bar, and the y-axis is the posterior probability. The three putative species are indicated below the individual ids

opennotspecifiedAug 2022View details →
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FIGURE 21. Habit and floral details. A in Can a rainbow consist of a single colour? A new comprehensive generic arrangement of the 'Iris sensu latissimo' clade (Iridaceae), congruent with morphology and molecular data

FIGURE 21. Habit and floral details. A) Zhaoanthus minutoaureus (Hooker 1910: t. 8293); B) Iridodictyum bakerianum (Foster 1889: t. 7084); C) Cryptobasis loczyi (photo: Georgy Lazkov); D) Cryptobasis mariae (photo: Elena Rahimova); E) Hermodactylus tuberosus (Syme 1869: t. 1496).

opennotspecifiedOct 2015View details →
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FIGURE 20 in Can a rainbow consist of a single colour? A new comprehensive generic arrangement of the 'Iris sensu latissimo' clade (Iridaceae), congruent with morphology and molecular data

FIGURE 20. Approximate distribution areas: A) Joniris (yellow); B) Cryptobasis (red); C) Syrianthus (green).

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FIGURE 15. Habit and floral details. A in Can a rainbow consist of a single colour? A new comprehensive generic arrangement of the 'Iris sensu latissimo' clade (Iridaceae), congruent with morphology and molecular data

FIGURE 15. Habit and floral details. A) Limniris sibirica (Dietrich 1832–1833: t. 45); B) L. tenax (Hooker 1834: t. 3343); C) L. pseudacorus (Lindman 1922–1926: t. 398); D) L. wilsonii (Smith 1910: t. 8340).

opennotspecifiedOct 2015View details →
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FIGURE 12 in Can a rainbow consist of a single colour? A new comprehensive generic arrangement of the 'Iris sensu latissimo' clade (Iridaceae), congruent with morphology and molecular data

FIGURE 12. Approximate distribution areas: A) Iris sect. Psammiris (yellow); B) I. sect. Oncocyclus (red); C) I. sect. Regelia (blue); D) I. sect. Pseudoregelia (violet).

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FIGURE 10 in Can a rainbow consist of a single colour? A new comprehensive generic arrangement of the 'Iris sensu latissimo' clade (Iridaceae), congruent with morphology and molecular data

FIGURE 10. Habit and floral details in habitat. A) Iris (Iris) lutescens (photo: Mario Martínez-Azorín); B) Iris (Psammiris) humilis (photo: Peter Bohnert); C) Iris (Oncocyclus) helena (photo: Ruslan Mishustin); D) Iris (Regelia) korolkowii (photo: Rafael Díez Domínguez); E) Iris (Pseudoregelia) dolichosiphon (photo: Rafael Díez Domínguez).

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FIGURE 19 in Can a rainbow consist of a single colour? A new comprehensive generic arrangement of the 'Iris sensu latissimo' clade (Iridaceae), congruent with morphology and molecular data

FIGURE 19. Approximate distribution areas: A) Eremiris (yellow); B) Sclerosiphon (green); C) Phaeiris (red); D) Zhaoanthus (blue); E) Hermodactylus (white).

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FIGURE 16 in Can a rainbow consist of a single colour? A new comprehensive generic arrangement of the 'Iris sensu latissimo' clade (Iridaceae), congruent with morphology and molecular data

FIGURE 16. Approximate distribution areas: A) Limniris sect. Limniris (red); B) L. sect. Chrysographes (violet); C) L. sect. Californicae (yellow); D) L. sect. Prismaticae (orange).

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FIGURE 9 in Can a rainbow consist of a single colour? A new comprehensive generic arrangement of the 'Iris sensu latissimo' clade (Iridaceae), congruent with morphology and molecular data

FIGURE 9. Approximate distribution areas: A) Pardanthopsis (violet); B) Belamcanda (orange); C) Juno (red); D) Junopsis (yellow). Areas for A and B include only the territories where they are presumably native.

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FIGURE 13. Habit and floral details. A in Can a rainbow consist of a single colour? A new comprehensive generic arrangement of the 'Iris sensu latissimo' clade (Iridaceae), congruent with morphology and molecular data

FIGURE 13. Habit and floral details. A) Juno persica (Wright 1906: t. 8059); B) Evansia japonica (Redouté 1806: t. 152); C) Junopsis collettii (Hooker 1903: t. 7889); D) Tectiris milesii (Baker 1886: t. 6889).

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FIGURE 18. Habit and floral details. A in Can a rainbow consist of a single colour? A new comprehensive generic arrangement of the 'Iris sensu latissimo' clade (Iridaceae), congruent with morphology and molecular data

FIGURE 18. Habit and floral details. A) Eremiris lactea (Lindley 1840: t. 1); B) Sclerosiphon songaricum (photo: Vladimir Kolobincev); C) Joniris ruthenica (photo: Aleksandr Kostjukov); D) Joniris ruthenica (Ker Gawler 1811: t. 1393); E) Phaeiris fulva (Small 1927: t. 388).

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FIGURE 4 in Can a rainbow consist of a single colour? A new comprehensive generic arrangement of the 'Iris sensu latissimo' clade (Iridaceae), congruent with morphology and molecular data

FIGURE 4. Flower morphology: falls, standards and stylar branches, sometimes with spathe bracts (cont.). A) Limniris sibirica (photo: Frank Hoehnel); B) Limniris chrysographes (photo: Ken Walker); C) Limniris sanguinea (photo: Andrej Baryshenko); D) Eremiris lactea (photo: Andrey Korzun); E) Sclerosiphon songaricum (photo: Vladimir Kolobincev); F) Joniris brevituba (photo: Georgy Lazkov); G) Phaeiris giganticaerulea (photo: Rodney Barton); H) Zhaoanthus henryi (photo: Ken Walker); I) Zhaoanthus minutoaureus (photo: Dennis Kramb); J) Iridodictyum reticulatum (photo: Sean Zera); K) Iridodictyum danfordiae (photo: Peter Bohnert); L) Cryptobasis mariae (photo: Yuriy Danilevsky).

opennotspecifiedOct 2015View details →
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FIGURE 6. Carpology. A in Can a rainbow consist of a single colour? A new comprehensive generic arrangement of the 'Iris sensu latissimo' clade (Iridaceae), congruent with morphology and molecular data

FIGURE 6. Carpology. A) Belamcanda chinensis, seeds black, long persistent on the central axis of fruit (photo: Stanislav Doronenko); B) Pardanthopsis dichotoma, seeds shortly winged (photo: Ken Walker); C) Gattenhofia verna var. smalliana, seeds with fleshy raphe and ribbed surface (photo: Ken Walker); D) Tectiris tectorum, seeds glossy, pyriform, apiculate, with inconspicuous aril (photo: Ken Walker); E) Evansia wattii, seeds matte, angulose, with small aril (photo: Dennis Kramb); F) Chamaeiris foetidissima, seeds reddish, persistent on valves of the opened fruit (photo: Ken Walker); G) Chamaeiris halophila, seeds with papery, loose testa (photo: David Pilling); H) Hermodactylus tuberosus, seeds globose with gelatinous aril (photo: Ken Walker); I) Lophiris cristata, seeds with long coiled appendage (photo: Jan Sacks); J) Zhaoanthus speculatrix, seeds with aril withering early as a wing (photo: Ken Walker); K) Phaeiris giganticaerulea, seeds large, flattened, with thickened, corky testa (photo: Robert R. Pries); L) Joniris uniflora, seeds with fleshy raphe vanishing on drying (photo: Robert R. Pries); M) Limniris sibirica, seeds discoidal, without aril, with subcorky testa (photo: Ken Walker); N) Rodionenkoa gracilipes, seeds with fleshy raphe and testa surface pitted (photo: Robert R. Pries); O) Junopsis collettii, seeds oblong with conspicuous whitish aril (photo: Ken Walker); P) Zhaoanthus koreanus, seeds globosecompressed, with fleshy raphe withering early as a wing (photo: Robert R. Pries); Q) Iris hoogiana, seeds with prominent aril and testa surface reticulate-wrinkled (photo: Robert R. Pries); R) Iris pumila, seeds without aril and testa surface reticulate-wrinkled (photo: Steve Hurst); S) Juno bucharica, seeds apiculate with fleshy appendage (photo: Ken Walker); T) Siphonostylis lazica, seeds angulose with testa surface covered with sessile glands (photo: Ken Walker). Scale bars in mm.

opennotspecifiedOct 2015View details →
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FIGURE 3 in Can a rainbow consist of a single colour? A new comprehensive generic arrangement of the 'Iris sensu latissimo' clade (Iridaceae), congruent with morphology and molecular data

FIGURE 3. Flower morphology: falls, standards and stylar branches in most cases, sometimes with spathe bracts. A) Siphonostylis lazica (photo: Ken Walker); B) Gattenhofia verna (photo: Jim McCormac); C) Pardanthopsis dichotoma (photo: Christy Hensler); D) Belamcanda chinensis, with all tepals subequal and also with fruits (photo: Tom Murphy); E) Iris germanica (photo: Ken Walker); F) Iris acutiloba (photo: Aleksandr Ivanov); G) Iris tigridia (photo: Vladimir Y. Arkhipov); H) Iris bloudowii (photo: Vesa Muurinen); I) Juno planifolia (photo: Mario Martínez-Azorín); J) Evansia japonica (photo: Ken Walker); K) Tectiris tectorum (photo: Ken Walker); L) Junopsis decora (photo: Ken Walker).

opennotspecifiedOct 2015View details →
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FIGURE 2 in Can a rainbow consist of a single colour? A new comprehensive generic arrangement of the 'Iris sensu latissimo' clade (Iridaceae), congruent with morphology and molecular data

FIGURE 2. External morphology of rootstock (bulbs, rhizomes and roots). A) Iridodictyum reticulatum, bulb with reticulate outer tunics (photo: Ken Walker); B) Xiphion heracleanum, bulb with membranous outer tunics and stem bulbil (photo: Manuel B. Crespo); C) Juno narbutii, bulb with persistent fleshy roots (photo: Ken Walker); D) Juno rosenbachiana, bulb with persistent fleshy roots (photo: Ken Walker); E) Limniris pseudacorus, rhizome with swollen annulate annual growths (photo: G.–U. Tolkiehn); F) Hermodactylus tuberosus, rhizome with pseudodigitate tubercles (photo: Attilio Marzorati); G) Junopsis barbatula, fleshy tuberous roots surrounding the inconspicuous central rhizome (photo: Ken Walker); H) Phaeiris hexagona, rhizome with fibrous remains of old leaves on scars, and fibrosus roots (photo: Ken Walker); I) Siphonostylis lazica, rhizome dichotomously branched and fibrous roots (photo: Ken Walker); J) Zhaoanthus odaesanensis, slender stoloniferous rhizomes with long, thin roots bearing nodules (photo: Christy Hensler); K) Rodionenkoa gracilipes, heterogeneous rhizome with cord-like branches (photo: Ken Walker); L) Cryptobasis bungei, short rizhomes with reddish-brown remains of leaf sheaths forming an apical neck-like structure (MO s.n.).

opennotspecifiedOct 2015View 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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