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Figs 9a–b in Development And Morphology Of Unduloribates Undulatus (Berlese, 1914) (Acari: Oribatida) And Some Remarks On The Unduloribatidae

Figs 9a–b. Interference contrast micrographs of egg exochorion structure: a = Unduloribates undulatus, b = Eupelops sp.

opencc-by-4.0May 2010View details →
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Fig. 6 in Developing Best Practice In Micropalaeontology: Examples From The Mid-Cretaceous Of The Zagros Mountains

Fig. 6 Further examples of relatively recent Zagros mid-Cretaceous biozonation schemes that utilize larger benthic foraminifera. No numerical scaling of the geological timescale is implied. The age assignments and taxonomic nomenclature are often outdat- ed, and the uncertainty precludes precise calibration of stage boundaries and the precise relationship of one zonal scheme to another.

opencc-by-4.0Feb 2022View details →
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Fig. 4 in Developing Best Practice In Micropalaeontology: Examples From The Mid-Cretaceous Of The Zagros Mountains

Fig. 4 Morphological variability (apical angle, test height and diameter) of the late Aptian – middle Albian Mesorbitolina texana (Roemer). a late Aptian Taft Formation of Central Iran. b late Aptian of Lebanon (from Schroeder and Neumann, 1985, pl. 36, fig. 2, topotype of Orbitolina discoidea var. libanica Henson; coll. F.R.S. Henson). Also note the convex test base in a and the central depression in b with a few final annular chambers.

opencc-by-4.0Feb 2022View details →
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Fig. 5 in Developing Best Practice In Micropalaeontology: Examples From The Mid-Cretaceous Of The Zagros Mountains

Fig. 5 Examples of relatively recent Zagros mid-Cretaceous biozonation schemes that utilize larger benthic foraminifera. No numerical scaling of the geological timescale is implied. The age assignments and taxonomic nomenclature are often outdated, and the uncertainty precludes precise calibration of stage boundaries and the precise relationship of one zonal scheme to another.

opencc-by-4.0Feb 2022View details →
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Fig. 2 in Developing Best Practice In Micropalaeontology: Examples From The Mid-Cretaceous Of The Zagros Mountains

Fig. 2 Lower- to mid-Cretaceous Orbitolinidae from Iran. a Subaxial section of Mesorbitolina sp. or Orbitolina sp. (= Dictyoconus pachymarginalis Schroeder in Dehghanian and Afghah, 2021, Fig. 7.4, Albian Kazhdumi Formation SW Iran). b–c Dictyoconus? pachymarginalis Schroeder, subaxial sections, Aptian Taft Formation, Central Iran. d "Dictyoconus pachymarginalis Schroeder" axial section (extracted from Afghah et al., 2014, fig. 11A), Cenomanian Sarvak Formation of SW Iran. e–f Persiconus sarvaki Yazdi-Moghadam & Schlagintweit, axial and tangential sections, Cenomanian Sarvak Formation of SW Iran.

opencc-by-4.0Feb 2022View details →
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Fig. 1 in Developing Best Practice In Micropalaeontology: Examples From The Mid-Cretaceous Of The Zagros Mountains

Fig. 1 Optimal and sub-optimal workflows for the identification of larger benthic foraminifera. Following a review of identification, the identity of a specimen can be confirmed or downgraded to a non-specific identity. If the identification is confident based on morphological features, stratigraphic range extension is possible, but should be evaluated carefully if the vast majority of well-established records suggest a different age.

opencc-by-4.0Feb 2022View details →
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Fig. 3 in Developing Best Practice In Micropalaeontology: Examples From The Mid-Cretaceous Of The Zagros Mountains

Fig. 3 Early – mid-Cretaceous Zagros biozonations (mostly assemblage zones or biofacies) utilising larger benthic foraminifera. The Wynd (1965) zonation and Sissingh (1977) zonations are based on data presented in Motiei (1993). Sampò (1969) and Kalantari (1976) are published schemes, whilst that of Ammen & Gharib (2014) is a scheme using more modern taxonomic concepts. LAD = Last Appearance Datum. FAD = First Appearance Datum. s.l. = sensu lato. No numerical scaling of the geological timescale is implied. The age assignments and taxonomic nomenclature are often outdated, and the uncertainty precludes precise calibration of stage boundaries and the precise relationship of one zonal scheme to another.

opencc-by-4.0Feb 2022View details →
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Comic strips sequences to develop narratives in the Storytelling in Sequence Task (STST)

<p>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; <strong>&nbsp; &nbsp; &nbsp; &nbsp;Comic strips sequences to develop narratives in theStorytelling in Sequence Task (STST)</strong></p> <p>&nbsp;&nbsp;</p> <p>The stimuli presented in the 9 following pages were developed by Sophie Courchesne and Sonia Routhier, under the supervision of Marion Fossard, as part of a master&rsquo;s essay in speech and language pathology at Laval University, Quebec City, Canada.</p> <p>The Storytelling in Sequence Task (STST) was then introduced in a paper of Fossard, Achim, et al., published in 2018 in the journal Frontiers in Psychology.</p> <p><strong>To cite this material :</strong></p> <p>Courchesne, S., &amp; Routhier, S. (2009). T&acirc;che de narration d&rsquo;histoires en s&eacute;quence et son analyse r&eacute;f&eacute;rentielle (Essai de ma&icirc;trise, Universit&eacute; Laval). Universit&eacute; Laval, Qu&eacute;bec, Canada.</p> <p>Fossard M, Achim AM (co-first authors), Roussier-Vercruyssen L, Gonzales S, Bureau A, Champagne-Lavau M. (2018). Referential choices in a collaborative storytelling task: Discourse stages and referential complexity matter. Frontiers in Psychology: Language Sciences, vol. 9, article 176. doi: 10.3389/fpsyg.2018.00176</p> <p><em>TERMES OF USE :</em> This material belongs to Marion Fossard and her research team. Its use is allowed in research or in clinical settings if the following conditions are met:</p> <div>&middot;All commercial use is prohibited;</div> <div>&middot;The source must be cited in all publications involving the use of this material;</div> <div>&middot;No Modifications must can made without the consent of Marion Fossard (<u><a href="mailto:marion.fossard@unine.ch">marion.fossard@unine.ch</a></u>);</div> <div>&middot;All clinical use is done while recognizing the limitations of the test.</div>

opencc-by-nc-nd-4.0Jul 2024View details →
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Fig. 2 in Two new Myxobolus spp. (Myxozoa: Myxobolidae) from white bream, Blicca bjoerkna (Linnaeus, 1758) developing in basifilamental location of gills

Fig. 2. Schematic illustration of Myxobolus spp. myxospores. a – M. bjoerknae sp. n. in frontal view, b – in sutural view; c – M. lamellobasis sp. n. in frontal view, d – in sutural view. Scale bar: 10 µm.

opencc-by-4.0Dec 2014View details →
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Fig. 3 in Two new Myxobolus spp. (Myxozoa: Myxobolidae) from white bream, Blicca bjoerkna (Linnaeus, 1758) developing in basifilamental location of gills

Fig. 3. Histological section of the cartilaginous gill arch of white bream. p – plasmodium of Myxobolus bjoerknae sp. n., c – cartilaginous base of the filaments, f – gill filament, ct – connective tissue; arrows indicate gill lamellae. Haematoxylin and eosin staining (H &amp; E). Scale bar: 100 µm.

opencc-by-4.0Dec 2014View details →
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Fig. 1. a in Two new Myxobolus spp. (Myxozoa: Myxobolidae) from white bream, Blicca bjoerkna (Linnaeus, 1758) developing in basifilamental location of gills

Fig. 1. a – spores of Myxobolus bjoerknae sp. n. infecting the cartilaginous gill arch in frontal view; inset: spores in sutural view; b – spores of M. lamellobasis sp. n. from the base of the gill filaments in frontal view; inset: spores in sutural view. Scale bars: 10 µm.

opencc-by-4.0Dec 2014View details →
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Fig. 5 in Two new Myxobolus spp. (Myxozoa: Myxobolidae) from white bream, Blicca bjoerkna (Linnaeus, 1758) developing in basifilamental location of gills

Fig. 5. Phylogenetic tree generated by Bayesian inference (GTR + I + Γ model) based on a 1613 bp-long alignment of 18S rDNA sequences of 43 myxosporean taxa. New Myxobolus spp. sequences are in bold. Ceratomyxa shasta was chosen as outgroup. Posterior probabilities are shown at nodes. NCBI accession numbers are in brackets.

opencc-by-4.0Dec 2014View details →
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Figure 5 in Development of a decision support system for managing Heterodera schahtii in sugar beet production

Figure 5: Crop sequence in rotation 4: tolerant sugar beets variety "Julietta"; Cereals; Cereals; "Julietta." The SBN initial population (Pi eggs g−1 soil) = 2.

opencc-by-4.0Apr 2019View details →
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Figure 6 in Development of a decision support system for managing Heterodera schahtii in sugar beet production

Figure 6: Crop sequence in rotation 5: tolerant sugar beets variety "Julietta"; Cereals; WOSR; Cereals; "Julietta." The SBN initial population (Pi eggs g−1 soil) = 2.

opencc-by-4.0Apr 2019View details →
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Fig. 1 in Development of habitat suitability criteria for Neotropical stream fishes and an assessment of their transferability to streams with different conservation status

Fig. 1. Location of the study sites in the São José dos Dourados River basin, São Paulo State, Brazil (a and b). Forested sites (dark circles) are located within the greatest forest fragments and deforested (gray circles) streams lack arboreal vegetation in their riparian zone and are located in areas dominated by pasture (c).

opencc-by-4.0Jun 2013View details →
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Fig. 2 in Development of habitat suitability criteria for Neotropical stream fishes and an assessment of their transferability to streams with different conservation status

Fig. 2. Habitat suitability criteria for depth and velocity of 10 species (codes in Table 1) developed for forested streams, considering five classes of depth (D1 = 0 to 0.2 m; D2 = 0.21 to 0.30 m; D3 = 0.31 to 0.40 m; D4 = 0.41 to 0.50 m; D5&gt; 0.51 m) and four classes of velocity (V1 =&gt; 0.0 to 0.2 m/s; V2 = 0.21 to 0.40 m/s; V3 = 0.41 to 0.60 m/s; V4&gt; 0.61 m/s). The dotted lines indicate SI = 0.7, above which conditions were considered optimal.

opencc-by-4.0Jun 2013View details →
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Fig. 8 in Reproductive cycle of the Neotropical cichlid yellow peacock bass Cichla kelberi: A novel pattern of testicular development

Fig. 8. Testicular morphological characteristics of the Regression phase in C. kelberi. (a) Testicular proximal region, highlighting the big volume of melano-macrophage centers (mmc). (b) Gonad in restructuration with details to the Sertoli cells phagocytizing (Sp) the residual sperm (rSz), and the apoptotic cells (double arrow). (c) Transversal section along the testis in Regression. (d) Testicular periphery (dorsal region) highlighting the intense proliferation of primary spermatogonia in this region (Sg). primary spermatogonial cluster (dotted line); I - interstitial tissue; Sp - Sertoli cell in phagocytosis; Sc1 - primary spermatocysts; Sg1 - primary spermatogonia; Sg2 - secondary spermatogonia. H.E. stain.

opencc-by-4.0Sep 2013View details →
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Fig. 7 in Reproductive cycle of the Neotropical cichlid yellow peacock bass Cichla kelberi: A novel pattern of testicular development

Fig. 7. Testicular morphological characteristics of Late GE Development phase in C. kelberi. (a) Longitudinal section of the main testicular duct (dt). (b) Germinal epithelium discontinuity in the distal region of the testicular lobules (asterisk). (c) Spermatogenic cysts in different development phases, highlighting the spermatocytes cyst in metaphase (mt) of the first meiotic division. (d) Discontinuity of the germinal epithelium along the testicle. H.E. stain. Egd - discontinuous germinal epithelium; mmc - melano-macrophage centers; S - Sertoli cell; Sc1 - primary spermatocysts; Sg1 -primary spermatogonia; Sg2 - secondary spermatogonia cysts; St - spermatids cysts; Sz - sperm. H.E. stain.

opencc-by-4.0Sep 2013View details →
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Fig. 6 in Reproductive cycle of the Neotropical cichlid yellow peacock bass Cichla kelberi: A novel pattern of testicular development

Fig. 6. Testicular morphological characteristics of Mid GE Development phase in C. kelberi. (a and b) Testicular anastomosing region, highlighting the beginning of the germinal epithelium discontinuity (asterisk), in both the anastomosing region and lobules near the main testicular ducts. (c) Discontinuous germinal epithelium, with cysts in different development stages and lots of sperm (Sz) in the lobular lumen. (d) Peripheral lobular region (dorsal) highlighting the continuous germinal epithelium and clusters of primary spermatogonia (dotted line). ar - anastomosing region; dt - main testicular ducts; I - interstice; m - basal membrane; mt - metaphase; S - Sertoli cell; Sc1 - primary spermatocysts; Sg1 - primary spermatogonia; Sg2 - secondary spermatogonia; St - spermatids; ta - tunica albuginea; cytoplasmic extension (hollow arrow). H.E. stain.

opencc-by-4.0Sep 2013View details →
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Fig. 5 in Reproductive cycle of the Neotropical cichlid yellow peacock bass Cichla kelberi: A novel pattern of testicular development

Fig. 5. Testicular morphological characteristics of Early GE Development phase in C. kelberi. (a) Main testicular duct region (dt), highlighting the narrow light (arrow). (b) Testicular lobules with continuous germinal epithelium (Egc) and germ cells cysts in different phases of spermatogenesis. (c) Germ cells cysts in different phases of spermatogenesis. (d) Distal lobular region, highlighting the germ cells clusters (dotted line). Bv - blood vessels; S - Sertoli cell; Sc1 - primary spermatocysts; Sg1 - primary spermatogonia; Sg2 - secondary spermatogonia; St - spermatids; ta - tunica albuginea. H. E. stain.

opencc-by-4.0Sep 2013View 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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