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Figure 22. Nepionts. A–G in Objective identification of Lepidocyclina (Foraminifera) species from the Eocene of Cuba based on growth-invariant morphometric characters

Figure 22. Nepionts. A–G, Lepidocyclina macdonaldi Cushman. Equatorial sections of megalospheric individuals. A, 98LC-1(640); B, 98LC-1(642); C, 98LC-1(616); D, 98LC-1(617); E, CA-215 (66); F, CA-215 (74); G, LM-23 (429). H, I, Lepidocyclina ariana Cole & Ponton. Equatorial sections of megalospheric individuals; H, LM-23(431); I, LM-23 (433). Loma Candela Formation (98LC-1), Arroyo Blanco Formation (CA-215) and Hatillo Formation (LM-23).

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Figure 20 in Objective identification of Lepidocyclina (Foraminifera) species from the Eocene of Cuba based on growth-invariant morphometric characters

Figure 20. Geometric reconstruction of chamberlets based on the means of character states for the species (Tables 5–8).

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Figure 19 in Objective identification of Lepidocyclina (Foraminifera) species from the Eocene of Cuba based on growth-invariant morphometric characters

Figure 19. Box plots of nepiont character states for the Lepidocyclina groups (species). Significant differences checked by the Kruskal-Wallis test. L. group 1 = L. macdonaldi, L. group 2 = L.?macdonaldi (small specimens), L. group 3 = L. ariana, L. group 4 = L. pustulosa, L. group 5 = L. ocalana.

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Figure 26 in Objective identification of Lepidocyclina (Foraminifera) species from the Eocene of Cuba based on growth-invariant morphometric characters

Figure 26. Lepidocyclina pustulosa (H. Douvilĺe). A–C, equatorial sections of megalospheric individuals; D–F, axial sections of megalospheric individuals; G–I, nepiont enlargement. A, G, LM-52(734); B, I, LM-52(738); C, H, LM-52(735); D, LM-52(742); E, LM-52(744); F, LM-52(751). Jabaco Formation (LM-52).

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Figure 21. A–G in Objective identification of Lepidocyclina (Foraminifera) species from the Eocene of Cuba based on growth-invariant morphometric characters

Figure 21. A–G, Lepidocyclina macdonaldi Cushman. Equatorial sections of megalospheric individuals. A, 98LC-1(640); B, 98LC-1(642); C, 98LC-1(616); D, 98LC-1(617); E, CA-215 (66); F, CA-215 (74); G, LM-23 (429); H, I, Lepidocyclina ariana Cole & Ponton. Equatorial sections of megalospheric individuals; H, LM-23(431); I, LM-23 (433). Loma Candela Formation (98LC-1), Arroyo Blanco Formation (CA-215) and Hatillo Formation (LM-23).

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Figure 15 in Objective identification of Lepidocyclina (Foraminifera) species from the Eocene of Cuba based on growth-invariant morphometric characters

Figure 15. Box plots of neanic character states for the Lepidocyclina groups (species). Significant differences checked by the Kruskal-Wallis test. L. group 1 = L. macdonaldi, L. group 2 = L.?macdonaldi (small specimens), L. group 3 = L. ariana, L. group 4 = L. pustulosa, L. group 5 = L. ocalana.

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Figure 17 in Objective identification of Lepidocyclina (Foraminifera) species from the Eocene of Cuba based on growth-invariant morphometric characters

Figure 17. Box plots of neanic character states for the Lepidocyclina groups (species). Significant differences checked by the Kruskal-Wallis test. L. group 1 = L. macdonaldi, L. group 2 = L.?macdonaldi (small specimens), L. group 3 = L. ariana, L. group 4 = L. pustulosa, L. group 5 = L. ocalana.

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Figure 13 in Objective identification of Lepidocyclina (Foraminifera) species from the Eocene of Cuba based on growth-invariant morphometric characters

Figure 13. Principal component analysis based on growth-independent characters of nepionts. Grouping by samples (point colours) and groups (background colour of convex hulls). Points with yellow margins represent the position of 'L. group 2'.

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Figure 12 in Objective identification of Lepidocyclina (Foraminifera) species from the Eocene of Cuba based on growth-invariant morphometric characters

Figure 12. Principal component analysis based on growth-invariant characters of neanic chamberlets. Grouping by samples (point colours) and groups (background colour of convex hulls). Points with yellow margins represent the position of 'L. group 2'.

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Figure 11 in Objective identification of Lepidocyclina (Foraminifera) species from the Eocene of Cuba based on growth-invariant morphometric characters

Figure 11. Loadings of the first and second axes in principal component analysis based on growth-independent and growth-invariant characters of neanic chamberlets and nepionts.

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Figure 14 in Objective identification of Lepidocyclina (Foraminifera) species from the Eocene of Cuba based on growth-invariant morphometric characters

Figure 14. Discriminant analysis separating species. Ellipses point to the 95% confidence limits. Axis values of characters shown in Table 3.

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Figure 10 in Objective identification of Lepidocyclina (Foraminifera) species from the Eocene of Cuba based on growth-invariant morphometric characters

Figure 10. Principal component analysis based on growth-independent and growth-invariant characters of neanic chamberlets and nepionts. Grouping by samples (point colours) and groups (background colour of convex hulls). Points with yellow margins represent the position of 'L. group 2' within 'L. group 1'.

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Figure 7 in Objective identification of Lepidocyclina (Foraminifera) species from the Eocene of Cuba based on growth-invariant morphometric characters

Figure 7. Growth functions of specimens pictured in Fig. 2, left for L. group 1, specimen 98C-1h(616), right for L. group 5, specimen P562(496).

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Figure 8 in Objective identification of Lepidocyclina (Foraminifera) species from the Eocene of Cuba based on growth-invariant morphometric characters

Figure 8. Growth functions of specimens pictured in Fig. 2, left for L. group 1, specimen 98C-1h(616), right for L. group 5, specimen P562(496).

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Figure 6 in Objective identification of Lepidocyclina (Foraminifera) species from the Eocene of Cuba based on growth-invariant morphometric characters

Figure 6. Lepidocyclina specimens with measurements of chamberlets (in sectors). 1070 measurements were taken for first and 1163 measurements for the second specimen demonstrating the high time and effort in measuring a single individual. A, 98C-1h(616) and B, P562(496).

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Figure 5 in Objective identification of Lepidocyclina (Foraminifera) species from the Eocene of Cuba based on growth-invariant morphometric characters

Figure 5. Measurements in equatorial sections: A, spatulate chamberlet; B, arcuate chamberlet; C, nepiont.

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Figure 3 in Objective identification of Lepidocyclina (Foraminifera) species from the Eocene of Cuba based on growth-invariant morphometric characters

Figure 3. Distribution of samples and assemblages LBF in Loma El Santo section, central Cuba (modified from Torres-Silva et al., 2019).

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Figure 2 in Objective identification of Lepidocyclina (Foraminifera) species from the Eocene of Cuba based on growth-invariant morphometric characters

Figure 2. Distribution of the samples and LBF assemblages at Loma Candelaria section, western Cuba (modified from Torres-Silva et al., 2019).

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Figure 4 in Objective identification of Lepidocyclina (Foraminifera) species from the Eocene of Cuba based on growth-invariant morphometric characters

Figure 4. Distribution of samples and LBF assemblages at Loma Viǵıa section, central Cuba (modified from Torres-Silva et al., 2019).

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Figure 1. A in Objective identification of Lepidocyclina (Foraminifera) species from the Eocene of Cuba based on growth-invariant morphometric characters

Figure 1. A, schematic tectonic map of western and central Cuba (after Iturralde-Vinent, 1994) with locations of the stratigraphical sections and samples. B, stratigraphical relations of the Eocene units in western and central Cuba slightly modified from Garćıa-Delgado & Torres-Silva (1997). Stratigraphical ranges of the studied sections, A (98LC-1), B (LM-52), C (LM-23), D (P-559, P-562), E (CA-215), F (CA-216).

opencc-by-4.0Feb 2024View 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