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FIG. 24 in Pliocene suids from Musaitu and Dermenji, Moldova: implications for understanding the origin of African Kolpochoerus Van Hoepen & Van Hoepen, 1932
FIG. 24. — Map of the Old World showing the reconstructed Plio-Pleistocene distribution of Dasychoerus Gray, 1873 (grey zones) (fossil localities: squares). The large square west of the Black Sea localises Musaitu and Dermenji, Moldova.
FIG. 15 in Pliocene suids from Musaitu and Dermenji, Moldova: implications for understanding the origin of African Kolpochoerus Van Hoepen & Van Hoepen, 1932
FIG. 15. — Right mandible of Dasychoerus arvernensis (Croizet & Jobert, 1828) from Dermenji, Moldova: A, lingual view; B, occlusal view; C, buccal view. Scale bar: 10 mm.
FIG. 19 in Pliocene suids from Musaitu and Dermenji, Moldova: implications for understanding the origin of African Kolpochoerus Van Hoepen & Van Hoepen, 1932
FIG. 19. — Length and breadth of lower cheek teeth of Dasychoerus arvernensis (Croizet & Jobert, 1828) from Europe and Africa (Mabaget Formation, Tugen Hills, Kenya). Symbols are the same as in Figures 16 and 17, except that the hollow snowflake symbol () in the middle line refers to the fossils from Mabaget.
FIG. 19. – Localisation des sources d in Les objets de parure associés au dépôt funéraire mésolithique de Grosse Ofnet: implications pour la compréhension de l'organisation sociale des dernières sociétés de chasseurs-cueilleurs du Jura Souabe
FIG. 19. – Localisation des sources d'approvisionnement des différents coquillages utilisés dans la parure de Grosse Ofnet. M, bassin de la Mayence; S, bassin de Stenheim; 1, Theodoxus gregarius; 2, Gyraulus sulcatus; 3, Lithoglyphus naticoides; 4, Columbella rustica.
FIG. 18 in Les objets de parure associés au dépôt funéraire mésolithique de Grosse Ofnet: implications pour la compréhension de l'organisation sociale des dernières sociétés de chasseurs-cueilleurs du Jura Souabe
FIG. 18. – Détails des perforations et usures de suspension observées sur les T. gregarius. Echelle du haut 1 cm, échelles A-D, 1 mm.
FIG. 17 in Les objets de parure associés au dépôt funéraire mésolithique de Grosse Ofnet: implications pour la compréhension de l'organisation sociale des dernières sociétés de chasseurs-cueilleurs du Jura Souabe
FIG. 17. – Détails des perforations et usures de suspension observées sur les L. naticoides. Echelle du haut 1 cm, échelles A-F, 1 mm.
FIG. 10 in Les objets de parure associés au dépôt funéraire mésolithique de Grosse Ofnet: implications pour la compréhension de l'organisation sociale des dernières sociétés de chasseurs-cueilleurs du Jura Souabe
FIG. 10. – Représentation du profil de mortalité des cerfs d'Ofnet projeté sur un diagramme ternaire (Stiner 1991, modifié selon Costamagno 1999). Ellipse de confiance 95% [Triangle 2.0 software (Boyko R., Weaver T., Steele T. in prep)].
FIG. 16 in Les objets de parure associés au dépôt funéraire mésolithique de Grosse Ofnet: implications pour la compréhension de l'organisation sociale des dernières sociétés de chasseurs-cueilleurs du Jura Souabe
FIG. 16. – Détails des perforations et usures de suspension observées sur les G. sulcatus. Echelle du haut 1 cm, échelles A-F, 1mm.
FIG. 6 in Les objets de parure associés au dépôt funéraire mésolithique de Grosse Ofnet: implications pour la compréhension de l'organisation sociale des dernières sociétés de chasseurs-cueilleurs du Jura Souabe
FIG. 6. – Canines de cerf appariées au sein de la collection de Ofnet (de haut en bas, paires de canines associées au crâne 18, 11, 6, 3). Echelle: 1 cm.
FIG. 9 in Les objets de parure associés au dépôt funéraire mésolithique de Grosse Ofnet: implications pour la compréhension de l'organisation sociale des dernières sociétés de chasseurs-cueilleurs du Jura Souabe
FIG. 9. – Attribution de l'âge des canines d'Ofnet: A,profil de l'âge des individus d'Ofnet estimé par l'équation basée sur les variables morphométriques; B, distribution des stades d'usure de la face occlusale. *1.75 ou 21 mois soit l'âge maximal pour l'éruption de la canine observé chez le cerf. (Mitchell 1967, Azorit et al. 2002).
FIG. 13 in Les objets de parure associés au dépôt funéraire mésolithique de Grosse Ofnet: implications pour la compréhension de l'organisation sociale des dernières sociétés de chasseurs-cueilleurs du Jura Souabe
FIG. 13. – Perforation des craches de cerf. Face linguale et vestibulaire de chaque crache, exemple de pièces associées au crâne n°3. Echelle 1 mm.
FIG. 7 in Les objets de parure associés au dépôt funéraire mésolithique de Grosse Ofnet: implications pour la compréhension de l'organisation sociale des dernières sociétés de chasseurs-cueilleurs du Jura Souabe
FIG. 7. – Comparaison du diamètre mésio-distal et vestibulo-lingual de la racine des pièces de Ofnet avec un référentiel de comparaison actuel (Rum), trois collections attribuées au Mésolithique récent (Braña-Arintero, Teviec, Hoëdic), ainsi que deux collections du Paléolithique Supérieur (Malataverne, Saint Germain la Rivière). Ellipse de confiance 95%.
FIG. 5 in Les objets de parure associés au dépôt funéraire mésolithique de Grosse Ofnet: implications pour la compréhension de l'organisation sociale des dernières sociétés de chasseurs-cueilleurs du Jura Souabe
FIG. 5. – Comparaison des diagrammes ternaires selon les méthodes de M.C. Stiner 1991 et S. Costamagno 1999.
FIG. 14. – Stades d in Les objets de parure associés au dépôt funéraire mésolithique de Grosse Ofnet: implications pour la compréhension de l'organisation sociale des dernières sociétés de chasseurs-cueilleurs du Jura Souabe
FIG. 14. – Stades d'usure des perforations observés sur les craches. Face linguale et vestibulaire de chaque crache. Echelle 1 mm.
Figure 2 in Reproductive ecology and behaviour of a species of Adenomera (Anura, Leptodactylinae) with endotrophic tadpoles: Systematic implications
Figure 2. The tadpole of Adenomera sp. Above: lateral view of the left side (scale bar: 4.0 mm). Below: detail of the oral apparatus (scale bar: 0.5 mm). Specimen from Uberlândia (MG, Brazil).
Figure 1 in Reproductive ecology and behaviour of a species of Adenomera (Anura, Leptodactylinae) with endotrophic tadpoles: Systematic implications
Figure 1. Rainfall in the municipality of Uberlândia. Lines represent median values over the last 21 years; columns represent values accumulated over the pitfall sampling period (seasons 1999/2000 and 2000/2001). Data from meteorological station of the Universidade Federal de Uberlândia (Campus Santa Mônica).
Figure 4 in Reproductive ecology and behaviour of a species of Adenomera (Anura, Leptodactylinae) with endotrophic tadpoles: Systematic implications
Figure 4. Oscillogram (first row), audiospectrogram (second and fourth rows) and power spectrum (third row) of the advertisement call of Adenomera sp. The first three rows are representations of single notes, the fourth represents a sequence of three notes. Recording files: first column, Adenomspmg2AAGd (17 December 2003, 17:00 h, air 24°C, unvouchered recording); second column, AdenomspmgAAGd (10 December 2003, 20:10 h, air 26°C, unvouchered recording); fourth row, AdenomspmgAAG21 (5 October 1999, 19:40 h, air 21°C, voucher AAG-UFU 2633).
Figure 3 in Reproductive ecology and behaviour of a species of Adenomera (Anura, Leptodactylinae) with endotrophic tadpoles: Systematic implications
Figure 3. Monthly variation in abundance of adults (males and females) and juveniles of Adenomera sp. in pitfall traps in two localities at the municipality of Uberlândia, Minas Gerais, Brazil. Above: Caça e Pesca sample (N572 adults, 32 juveniles). Below: Panga sample (N513 adults and 13 juveniles). Sampling period from October 1999 to October 2001. The monthly samples are not independent, since the trapped specimens were removed from the environment.
Figure 5 in Reproductive ecology and behaviour of a species of Adenomera (Anura, Leptodactylinae) with endotrophic tadpoles: Systematic implications
Figure 5. Territorial call of Adenomera sp. Above left: audiospectrogram of a sequence of three calls. Above right: oscillogram of single note. Below left: audiospectrogram of single note. Below right: power spectrum of single note. Record file AdenomspmgbAAG27, 14 November 2002, 20:30 h, air 23.0°C (unvouchered).
Growth genes are implicated in the evolutionary divergence of sympatric piscivorous and insectivorous rainbow trout (Oncorhynchus mykiss)
<p>Identifying ecologically significant phenotypic traits and the genomic mechanisms that underly them are crucial steps in understanding the traits associated with population divergence. We used genome-wide data to identify genomic regions associated with a key trait that distinguishes two ecotypes of rainbow trout (Oncorhynchus mykiss) – insectivores and piscivores – that coexist in Kootenay Lake, southeastern British Columbia, for the non-breeding portion of the year. "Gerrards" are large-bodied (breeding maturity at >60cm) piscivores that spawn 50km north of Kootenay Lake in the Lardeau River, in contrast to the insectivorous populations that are on average smaller in body size, mainly forage on aquatic insects, and spawn in tributaries immediately surrounding Kootenay Lake. We used pool-seq data covering 60 percent of the genome to assess the level of genomic divergence between ecotypes, test for genotype-phenotype associations, and identify loci that may play functional or selective roles in their divergence. Analysis of nearly seven million SNPs provided a genome-wide mean FST estimate of 0.18, indicating a high level of reproductive isolation between populations. The window-based FST analysis did not reveal "islands" of genomic differentiation; however, the window with highest FST estimate did include a gene associated with insulin secretion. Although we explored the use of the "Local score" approach to identify genomic outlier regions, this method was ultimately not used because simulations revealed a high false discovery rate (20 percent). Gene Ontology (GO) analysis identified several growth processes as enriched in genes occurring in the 200 most divergent genomic windows, indicating the importance of genetically-based growth and growth-related metabolic functions in the divergence of these ecotypes. In spite of their sympatric coexistence, a high degree of genomic differentiation separates the populations of piscivores and insectivores, indicating little to no contemporary genetic exchange between ecotypes. Our results further indicate that the large body piscivorous 27 phenotype is likely not due to one or a few loci of large effect, rather it may be controlled by several loci of small effect, thus highlighting the power of whole-genome low-coverage sequencing in phenotypic association studies.</p>
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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.
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.
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.
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.
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.