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zenodo40/100

Fig. 3 in Capalictus, a new subgenus of Lasioglossum Curtis, 1833 from South Africa, with description of three new species (Hymenoptera, Apoidea, Halictidae)

Fig. 3. Lasioglossum (Capalictus) mosselinum (Cockerell, 1945), Ƌ. A. Head. B. Mesoscutum and vertex. C. Propodeum. D. First tergum. E. Metasoma, dorsal view. F. Metasoma, ventral view. Scale line = 0,5 mm.

opencc-by-3.0Nov 2012View details →
zenodo40/100

Fig. 8 in Capalictus, a new subgenus of Lasioglossum Curtis, 1833 from South Africa, with description of three new species (Hymenoptera, Apoidea, Halictidae)

Fig. 8. Lasioglossum (Capalictus) timmermanni sp. nov., Ƌ. A. Head. B. Mesosoma and vertex. C. Propodeum and metanotum. D. First tergum. E. Metasoma, dorsal view. F. Metasoma, ventral view. Scale line = 0,5 mm.

opencc-by-3.0Nov 2012View details →
zenodo40/100

Fig. 9 in Capalictus, a new subgenus of Lasioglossum Curtis, 1833 from South Africa, with description of three new species (Hymenoptera, Apoidea, Halictidae)

Fig. 9. Lasioglossum (Capalictus) timmermanni sp. nov., ♀. A. Head. B. Mesoscutum and scutellum. C. Propodeum. D. Metanotum. E. Metasoma. F. First tergum. Scale line = 0,5 mm.

opencc-by-3.0Nov 2012View details →
dryad40/100

Data from: Genome wide assessment of genetic variation and population distinctiveness of the pig family in South Africa

<p>Genetic diversity is of great importance and a prerequisite for genetic improvement and conservation programs in pigs and other livestock populations. The present study provides a genome wide analysis of the genetic variability and population structure of pig populations from different production systems in South Africa relative to global populations. A total of 234 pigs sampled in South Africa and consisting of village (n = 91), commercial (n = 60), indigenous (n = 40), Asian (n = 5) and wild (n = 38) populations were genotyped using Porcine SNP60K BeadChip. In addition, 389 genotypes representing village and commercial pigs from America, Europe and Asia were accessed from a previous study and used to compare population clustering and relationships of South African pigs with global populations. Moderate heterozygosity levels, ranging from 0.204 for Warthogs to 0.371 for village pigs sampled from Capricorn municipality in Eastern Cape province of South Africa were observed. Principal Component Analysis of the South African pigs resulted in four distinct clusters of (i) Duroc; (ii) Vietnamese; (iii) Bush pig and Warthog and (iv) a cluster with the rest of the commercial (SA Large White and Landrace), village, Wild Boar and indigenous breeds of Koelbroek and Windsnyer. The clustering demonstrated alignment with genetic similarities, geographic location and production systems.  The PCA with the global populations also resulted in four clusters that where populated with (i) all the village populations, wild boars, SA indigenous and the large white and landraces; (ii) Durocs (iii) Chinese and Vietnamese pigs and (iv) Warthog and Bush pig. <i>K</i>= 10 (The number of population units) was the most probable ADMIXTURE based clustering, which grouped animals according to their populations with the exception of the village pigs that showed presence of admixture. AMOVA reported 19.92% – 98.62% of the genetic variation to be within populations. Sub structuring was observed between South African commercial populations as well as between Indigenous and commercial breeds. Population pairwise <i>F<sub>ST</sub></i>analysis showed genetic differentiation <i>(P &lt; 0.05)</i>between the village, commercial and wild populations. A per marker per population pairwise <i>F<sub>ST</sub></i>analysis revealed SNPs associated with QTLs for traits such as meat quality, cytoskeletal and muscle development, glucose metabolism processes and growth factors between both domestic populations as well as between wild and domestic breeds. Overall, the study provided a baseline understanding of porcine diversity and an important foundation for porcine genomics of South African populations.</p>

opencc-zeroJun 2020View details →
zenodo40/100

Fig. 7 in Revalidation of Enteromius alberti and presence of Enteromius cf. mimus (Cypriniformes: Cyprinidae) in the Lake Edward system, East Africa

Fig. 7. (a) Lectotype of Enteromius alberti (Poll, 1939) (MRAC 64723) with 74.3 mm SL. (b) Fresh specimen of E. alberti (RMCA 2018.008.P.0248 HP 3246) with 62.4 mm SL.

opencc-by-4.0Aug 2020View details →
zenodo40/100

Fig. 4 in Revalidation of Enteromius alberti and presence of Enteromius cf. mimus (Cypriniformes: Cyprinidae) in the Lake Edward system, East Africa

Fig. 4. Scatterplots of PC2 against PC1 of the PCA on (a) 24 log-transformed measurements (n = 69) and (b) on 15 meristics (n = 62). Specimens of group A, the filled circles (●) represent the genetically analysed specimens, the open circles (Ǫ) indicate the additional specimens. Specimens of E. alberti (Poll, 1939) (lectotype) (♦), E. alberti (paralectotypes) (◊), specimens from Tshambi (), E. cercops (Whitehead, 1960) (holotype) (▲), E. cercops (paratypes) (), E. mimus (Boulenger, 1912) (lectotype) (▼), E. mimus (paralectotypes) (▼), E. perince (R̹ppell, 1835) (syntypes) (+) and E. stigmatopygus (Boulenger, 1903) (syntypes) (×).

opencc-by-4.0Aug 2020View details →
zenodo40/100

Fig. 6 in Revalidation of Enteromius alberti and presence of Enteromius cf. mimus (Cypriniformes: Cyprinidae) in the Lake Edward system, East Africa

Fig. 6. Scatterplot of PC2 against PC1 of the PCA (n = 83) on 24 log-transformed measurements. For group B, the filled squares (■) represent the specimens used for the genetic analysis, the open squares (□) indicate the additional specimens of the Lake Edward system and the two specimens from Tshambi. Specimens of E. mimus (Boulenger, 1912) (lectotype) (▼) and E. mimus (paralectotypes) (▼).

opencc-by-4.0Aug 2020View details →
zenodo40/100

Fig. 2 in Revalidation of Enteromius alberti and presence of Enteromius cf. mimus (Cypriniformes: Cyprinidae) in the Lake Edward system, East Africa

Fig. 2. Scatterplot of PC2 against PC1 of a PCA on 24 log-transformed measurements on 71 specimens of Enteromius Cope, 1867. Specimens of the genetic groups A (●) (n = 21) and B (■) (n = 50) are indicated separately.

opencc-by-4.0Aug 2020View details →
zenodo40/100

Fig. 5 in Revalidation of Enteromius alberti and presence of Enteromius cf. mimus (Cypriniformes: Cyprinidae) in the Lake Edward system, East Africa

Fig. 5. Scatterplots of PC2 against PC1 of (a) the PCA (n = 105) on 24 log-transformed measurements and (b) the PCA (n = 95) on 15 meristics. Specimens of group B, the filled squares (■) represent the genetic analysed specimens, the open squares (□) indicate the additional specimens. Specimens of E. alberti (Poll, 1939) (lectotype) (♦), E. alberti (paralectotypes) (◊), specimens from Tshambi (), E. cercops (Whitehead, 1960) (holotype) (▲), E. cercops (paratypes) (), E. mimus (Boulenger, 1912) (lectotype) (▼), E. mimus (paralectotypes) (▼), E. perince (R̹ppell, 1835) (syntypes) (+) and E. stigmatopygus (Boulenger, 1903) (syntypes) (×).

opencc-by-4.0Aug 2020View details →
zenodo40/100

Fig. 1 in Revalidation of Enteromius alberti and presence of Enteromius cf. mimus (Cypriniformes: Cyprinidae) in the Lake Edward system, East Africa

Fig. 1. Haplotype network of 651-bp-long COI sequences (n = 137) of the specimens of Enteromius Cope, 1867 with a smooth, flexible last unbranched dorsal fin ray from the Lake Edward system. Each circle represents a haplotype, with the size of the circles indicating the number of individuals with this haplotype and the colour indicating the different parts of the basin. Each bar represents a mutation between two haplotypes.

opencc-by-4.0Aug 2020View details →
zenodo40/100

Fig. 3 in Revalidation of Enteromius alberti and presence of Enteromius cf. mimus (Cypriniformes: Cyprinidae) in the Lake Edward system, East Africa

Fig. 3. Scatterplots of (a) interorbital width (IOW), (b) pre-pelvic distance (PrPelD), (c) body depth (BD), (d) maximum caudal peduncle depth (MxCPD), (e) minimum caudal peduncle depth (MnCPD), (f) head width (HW), and (g) head depth (HD) in % SL against SL (in mm) on 72 specimens of Enteromius Cope, 1867. The genetic groups A (●) (n = 22) and B (■) (n = 50) are indicated separately. The dashed lines indicate the size class used for the MWU tests.

opencc-by-4.0Aug 2020View details →
zenodo40/100

Figure 3 in Aspects of natural history in a sand boa, Eryx muelleri (Erycidae) from arid savannahs in Burkina Faso, Togo, and Nigeria (West Africa)

Figure 3. Relationships between (a) Snout-Vent-Length (SLV) and Tail Length (TL), and between (b) SVL and Head Length (HL) in Eryx muelleri. Specimens from Togo, Burkina Faso and Nigeria were pooled.

opencc-by-4.0Aug 2015View details →
zenodo40/100

Figure 1 in Aspects of natural history in a sand boa, Eryx muelleri (Erycidae) from arid savannahs in Burkina Faso, Togo, and Nigeria (West Africa)

Figure 1. (a) Eryx muelleri from Kebbe, north-western Nigeria (Photo: Luca Luiselli); (b) dry savannah habitat of Eryx muelleri in northern Burkina Faso (Photo: Emmanuel Hema).

opencc-by-4.0Aug 2015View details →
zenodo40/100

Filling Africa's largest hydropower dam should consider engineering realities

<p>This repository contains engineering data for the Grand Ethiopian Renaissance Dam, including reservoir geometry, evaporation rates, tailwater curve, and outlet capacities.</p>

opencc-by-4.0Aug 2020View details →
zenodo40/100

Figure 5 in A new large and colourful species of the genus Doto (Nudibranchia: Dotidae) from South Africa

Figure 5. Living specimens. (A) Doto coronata (Gmelin, 1791). Specimen from Northern Ireland. Photo by Bernard Picton; (B) Doto cf. coronata. Specimen from South Africa, Cape Province, Oudekraal. Photo by T.M. Gosliner; (C) Doto rosea Trinchese, 1881. Specimen from Catalunia, Spain Photo by Antoni López-Arenas; (D) Doto pinnatifida (Montagu, 1804). Specimen from Northern Ireland. Photo by Bernard Picton.

opencc-by-4.0Apr 2015View details →
zenodo40/100

Figure 2 in A new large and colourful species of the genus Doto (Nudibranchia: Dotidae) from South Africa

Figure 2. Doto splendida nov. sp. Paratype (CASIZ176123), SEM pictures of the radula and penis. (A) Radula, scale bar: 10 μm; (B) detail of the teeth, scale bar: 3 μm; (C) penis, scale bar: 10 μm; (D) detail of the penis, scale bar: 10 μm.

opencc-by-4.0Apr 2015View details →
zenodo40/100

Figure 3 in A new large and colourful species of the genus Doto (Nudibranchia: Dotidae) from South Africa

Figure 3. Reproductive system of Doto splendida nov. sp. Paratype (CASIZ176123). Abbreviations: am, ampulla; fglm, female gland mass; hd, hermaphrodite duct; ov, oviduct; pb, penial bulb; pr, prostate; sr, seminal receptacle; v, vagina; vd, vas deferens. Scale bars, 1 mm.

opencc-by-4.0Apr 2015View details →
zenodo40/100

Figure 9 in Revision of the genus Delopleurus Boheman (Coleoptera: Scarabaeidae: Scarabaeinae) with description of new species from Africa

Figure 9. Delopleurus spp. and Metacatharsius janssensi. (A, E) habitus (A, D. striatus, E, M. janssensi); (B) D. striatus, head and pronotum in dorsal view; (C) D. striatus, pygidium; (D) D. striatus, locality map; (F) D. fossatus sp. nov., ventral view of head showing gula with distinct longitudinal groove.

opencc-by-4.0Jun 2014View details →
zenodo40/100

Figure 8 in Revision of the genus Delopleurus Boheman (Coleoptera: Scarabaeidae: Scarabaeinae) with description of new species from Africa

Figure 8. Delopleurus parvus. (A, D) habitus (A, male, D, female); (B, E) pygidium (B, male, E, female); (C) aedeagus in lateral view and internal sac; (F) locality map.

opencc-by-4.0Jun 2014View details →
zenodo40/100

Figure 4 in Revision of the genus Delopleurus Boheman (Coleoptera: Scarabaeidae: Scarabaeinae) with description of new species from Africa

Figure 4. Delopleurus darrenmanni sp. nov. (A, D) habitus (A, male, D, female); (B, E) pygidium (B, male, E, female); (C) aedeagus in lateral view and internal sac; (F) locality map.

opencc-by-4.0Jun 2014View 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