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Fig. 35 in "Larger" Benthic Foraminifera Of The Cenomanian. A Review Of The Identity And The Stratigraphic And Palaeogeographic Distribution Of Non-Fusiform Planispiral (Or Near-Planispiral) Forms

Fig. 35 Representative illustrations of Hemicyclammina whitei: a Axial view, Whittaker et al. (1998, pl. 12, fig. 1a, Qatar - see also Simmons & Bidgood, 2022, fig. 1a); b Axial section, Whittaker et al. (1998, pl. 59, fig. 8, U.A.E. - see also Simmons & Bidgood, 2022, fig. 3c); c Equatorial section, Simmons & Bidgood (2022, fig. 3a, Abu Dhabi).

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Fig. 37 in "Larger" Benthic Foraminifera Of The Cenomanian. A Review Of The Identity And The Stratigraphic And Palaeogeographic Distribution Of Non-Fusiform Planispiral (Or Near-Planispiral) Forms

Fig. 37 Representative illustrations of Reissella ramonensis: a Exterior view, (Hamaoui 1963, pl. 1, fig. 3, holotype, Israel); b Exterior view (schematic), (Hamaoui 1963, pl. 1, fig. 11, Israel); c Enlarged cutaway exterior view showing internal features (Hamaoui 1963, text fig. 1, Israel).

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Fig. 21 in "Larger" Benthic Foraminifera Of The Cenomanian. A Review Of The Identity And The Stratigraphic And Palaeogeographic Distribution Of Non-Fusiform Planispiral (Or Near-Planispiral) Forms

Fig. 21 Representative illustrations of Charentia cuvillieri: a Equatorial section, Neumann (1965, holotype, pl. 2, fig. 1c, France); b Axial section, Schroeder & Neumann (1985, pl. 3, fig. 3, France).

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Fig. 29 in "Larger" Benthic Foraminifera Of The Cenomanian. A Review Of The Identity And The Stratigraphic And Palaeogeographic Distribution Of Non-Fusiform Planispiral (Or Near-Planispiral) Forms

Fig. 29 Representative illustrations of Buccicrenata ex gr. subgoodlandensis: a Uncoiled equatorial section, Loeblich & Tappan (1985, pl. 2, fig. 7, Texas); b Close up of section through wall and septum, Loeblich & Tappan (1985, pl. 2, fig. 10, Texas); c Equatorial section, Loeblich & Tappan (1985, pl. 2, fig. 5, Texas); d External view, Loeblich & Tappan (1985, pl. 2, fig. 9, Texas).

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Fig. 33 in "Larger" Benthic Foraminifera Of The Cenomanian. A Review Of The Identity And The Stratigraphic And Palaeogeographic Distribution Of Non-Fusiform Planispiral (Or Near-Planispiral) Forms

Fig. 33 Representative illustrations of Pseudocyclammina sarvakensis: a Equatorial section, Schlagintweit & Yazdi-Moghadam (2023, fig. 4b, Iran, holotype); b Subaxial section, Ibid. (2023, fig. 4d, Iran); c Oblique tangential section, Ibid. (2023, fig. 4f, Iran). Not scale bar change for figs. b & c.

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Fig. 23 in "Larger" Benthic Foraminifera Of The Cenomanian. A Review Of The Identity And The Stratigraphic And Palaeogeographic Distribution Of Non-Fusiform Planispiral (Or Near-Planispiral) Forms

Fig. 23 Representative illustrations of Fleuryana gediki: a Equatorial section, Solak et al. (2020, fig. 15(R), Turkey); b Axial section, Solak et al. (2020, fig. 15(S), Turkey).

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Fig. 31 in "Larger" Benthic Foraminifera Of The Cenomanian. A Review Of The Identity And The Stratigraphic And Palaeogeographic Distribution Of Non-Fusiform Planispiral (Or Near-Planispiral) Forms

Fig. 31 Representative illustrations of Pseudocyclammina rugosa: a Equatorial section, Maync (1952, pl. 12, fig. 9, France); b Equatorial section of uncoiled specimen, Maync (1959b, pl. 1, fig. 14, France); c Axial section, Maync (1952, pl. 12, fig. 8, France).

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FIGURE 15 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain

FIGURE 15 Light micrographs of Longidorus pini Andrés and Arias, 1988 paratypes from San Martín del Pimpollar, Avila province (A–F), and the population from Nava de Francia, Salamanca province (G–M). A–C, G–I, female anterior regions. D–F, J–K, female tails. L-M, male tail with detail of spicules. Abbreviations: a = anus; gr = guiding ring; sp = spicules; spl = ventromedian supplements. Scale bars = 20 μm

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FIGURE 13 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain

FIGURE 13 Light micrographs of Longidorus cf. olegi Kankina & Metlitskaya, 1983. (A)–(B) female anterior region. (C)–(F) female lip regions. (G) detail of basal bulb. (H) vulval region. (I)–(L) female tails. (M) and (N), male tail with detail of spicules. (O)–(R) First-, second-, third-, and fourth-stage juvenile (J1–J4) tails, respectively. Abbreviations: a = anus; af = amphidial fovea; gr = guiding ring. Scale bars = 20 μm

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FIGURE 14 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain

FIGURE 14 Relationship of body length to length of functional and replacement odontostyle (Ost and rOst, respectively) length in all developmental stages from first-stage juveniles (J1) to mature females of Longidorus cf. olegi Kankina & Metlitskaya, 1983

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FIGURE 12 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain

FIGURE 12 Light micrographs of Longidorus nevesi Macara 1985. (A) female anterior region. (B) female lip region. (C) vulval region. (D) female tail. (E)–(F) male tail with detail of spicules. Abbreviations: a = anus; gr = guiding ring; spl = ventromedian supplements; V = vulva. Scale bars = 20 μm

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Figure 11 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain

Figure 11 Light micrographs of Longidorus carpetanensis Arias et al., 1986 from Puebla de Sanabria, Zamora (A)–(F), and topotypes from Navalmoral, Avila (G)–(L). A–C, G and H, female anterior regions. D, I, female tails. E and F, J and L, male tail with detail of spicules. Abbreviations: a = anus; gr = guiding ring; spl = ventromedian supplements. Scale bars = 20 µm

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FIGURE 9 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain

FIGURE 9 Light micrographs of Longidorus pacensis sp. nov. (A)–(G) Anterior regions. (H) Vulval region. (I)–(K) Female tails. (L) Detail of sperm cells. (M) and (N) Male tails. (O)–(R) First-, second-, third-, and fourth-stage juvenile (J1–J4) tails, respectively. Abbreviations: a = anus; af = amphidial fovea; gr = guiding ring; sp = spicules; spl = ventromedian supplements; v = vulva. Scale bars = 20 μm

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FIGURE 10 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain

FIGURE 10 Light micrographs of Longidorus africanus Merny, 1966. (A) female anterior region. (B) female lip region. (C) vulval region. (D)–(E) female tails. Abbreviations: a = anus; gr = guiding ring; v = vulva. Scale bars = 20 μm

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FIGURE 8 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain

FIGURE 8 Line drawings of Longidorus pacensis sp. nov. (A) Female neck region. (B) and (C) Female lip regions. (D) and (E) Female tails. (F) Male tail. (G) First-stage juvenile tail

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FIGURE 7 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain

FIGURE 7 Relationship of body length to length of functional and replacement odontostyle (Ost and rOst, respectively) length in all developmental stages from first-stage juveniles (J1) to mature females of. (A) Longidorus iliturgiensis sp. nov. (B) Longidorus pacensis, sp. nov.

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FIGURE 4 Phylogenetic relationships within the genus Longidorus. Bayesian 50 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain

FIGURE 4 Phylogenetic relationships within the genus Longidorus. Bayesian 50% majority rule consensus tree as inferred from cytochrome c oxidase subunit I (CoxI) mtDNA gene sequence alignment under the general time-reversible model of sequence evolution with correction for invariable sites and a gammashaped distribution (GTR + I + G). Posterior probabilities greater than 0.70 are given for appropriate clades. Newly obtained sequences in this study are shown in bold. Scale bar = expected changes per site.

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FIGURE 6 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain

FIGURE 6 Light micrographs of Longidorus iliturgiensis, sp. nov. (A)–(D) Anterior regions. (E) Vulval region. (F)–(I) Female tails. (J)–(M) First-, second-, third-, and fourth-stage juvenile (J1–J4) tails, respectively. (N)–(O) Male tail. Abbreviations: a = anus; af = amphidial fovea; spl = ventromedian supplements; v = vulva. Scale bars (A)–(C), (E)–(O) = 20 μm; (D) = 10 μm

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FIGURE 5 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain

FIGURE 5 Line drawings of Longidorus iliturgiensis, sp. nov. paratypes. (A) Female neck region. (B) and (C) Female lip regions. (D) and (E) Female tails. (F) Male tail. (G) First-stage juvenile tail

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FIGURE 3 Phylogenetic relationships within the genus Longidorus. Bayesian 50 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain

FIGURE 3 Phylogenetic relationships within the genus Longidorus. Bayesian 50% majority rule consensus tree as inferred from 18S rRNA gene sequence alignment under a transitional model with invariable sites and a gamma correction (TIM 2 + I + G). Posterior probabilities greater Downloaded than 0.70 from are Brill given.comfor08/29/ appropriate 2023 05:44:51PM clades. Newly obtained sequences in this study are shown in bold. Scale bar = expected changesvia per site free. access

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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