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Fig. 2 in Nest support plants and breeding season of two ibis (Theristicus) species in the Pantanal wetland, Brazil
Fig. 2. Seasonal occurrence of records of breeding activities of two ibis species (Theristicus caerulescens and T. caudatus) in the Brazilian Pantanal wetland, based on records (photographs) obtained during our field observations, and bY citizens, between 2007 and 2019. Data bY citizens was gathered in the WikiAves and eBird databases in March 2020. The horizontal bars in light and dark blue colors indicate the length of the dry and rainy seasons in the Pantanal, respectively.
Figs 1, 2 in Two new species of oil-collecting bees of Centris (Melanocentris) from Colombia (Hymenoptera: Apidae)
Figs 1, 2. Centris (Melanocentris) germani sp. nov., holotype male:1, frontal view (scale bar 2 mm); 2, habitus, lateral view (scale bar 5 mm).
Figs 3, 4 in Two new species of oil-collecting bees of Centris (Melanocentris) from Colombia (Hymenoptera: Apidae)
Figs 3, 4. Centris (Melanocentris) marinae sp. nov., holotype male: 1, frontal view (scale bar 2 mm); 2, habitus, lateral view (scale bar 5 mm).
Fig. 5 in Two new species of oil-collecting bees of Centris (Melanocentris) from Colombia (Hymenoptera: Apidae)
Fig. 5. Distribution records of Centris (Melanocentris) germani sp. nov. and C. (Melanocentris) marinae sp. nov.
Fig. 2 in Comparative analysis of the diet of Arctocephalus gazella (Pinnipedia), at two localities of the South Shetland Islands, with emphasis on the fish component
Fig. 2. Estimated standard length frequency distribution of Gymnoscopelus nicholsi (Gilbert, 1911), preyed on by Antarctic fur seals Arctocephalus gazella (Peters, 1875), at Stranger Point and Duthoit Point, South Shetland Islands, in February 2012.
Fig. 1 in Comparative analysis of the diet of Arctocephalus gazella (Pinnipedia), at two localities of the South Shetland Islands, with emphasis on the fish component
Fig. 1. The study area at South Shetland Islands: Stranger Point, King George Island/Isla 25 de Mayo and Duthoit Point, Nelson Island (modified from MALVÉ et al., 2014 and BRAUN et al., 2017).
Fig. 4 in Comparative analysis of the diet of Arctocephalus gazella (Pinnipedia), at two localities of the South Shetland Islands, with emphasis on the fish component
Fig. 4. Estimated standard length frequency distribution of Electrona antarctica (Gunther, 1878) preyed on by Arctocephalus gazella (Peters, 1875), at both sampling sites, Stranger Point and Duthoit Point, South Shetland Islands, in February 2012.
Fig. 3 in Comparative analysis of the diet of Arctocephalus gazella (Pinnipedia), at two localities of the South Shetland Islands, with emphasis on the fish component
Fig. 3. Estimated standard length frequency distribution of Pleuragramma antarctica (Boulenger, 1902) preyed on by Arctocephalus gazella (Peters, 1875), at both sampling sites, Stranger Point and Duthoit Point, South Shetland Islands, in February 2012.
Fig. 2 in The importance of considering small-scale variability in macrobenthic distribution: spatial segregation between two fiddler crab species (genus Leptuca) (Decapoda, Ocypodidae)
Fig. 2. NMDS ordination (stress = 0.16) of sites based on similarity of group composition. Leptuca leptodactyla (Rathbun in Rankin, 1898): JLM (juvenile males), JLF (juvenile females), ALM (adult males) and ALF (adult females). Leptuca uruguayensis (Nobili, 1901): JUM (juvenile males), JUF (juvenile females), AUM (adult males) and AUF (adult females).
Fig. 2 in Temporal variations of larval digenean assemblages parasitizing Heleobia parchappii (Mollusca: Cochliopidae) in two shallow lakes from the Buenos Aires province, Argentina
Fig. 2. Seasonal variation in the Overall prevalence (mean ± S.D) of larval digeneans parasitizing Heleobia parchappii (D'Orbigny, 1835) in Los Padres and La Brava lakes, Buenos Aires province, Argentina.
Fig. 1 in The importance of considering small-scale variability in macrobenthic distribution: spatial segregation between two fiddler crab species (genus Leptuca) (Decapoda, Ocypodidae)
Fig. 1. Schematic representation of the sampling design, with subarea separation and the six random replicates. (Area=10 m²).
Fig. 3 in Temporal variations of larval digenean assemblages parasitizing Heleobia parchappii (Mollusca: Cochliopidae) in two shallow lakes from the Buenos Aires province, Argentina
Fig. 3. Seasonal variation in Species richness (mean ± S.D) of larval digeneans parasitizing Heleobia parchappii (D'Orbigny, 1835) in Los Padres and La Brava lakes, Buenos Aires province, Argentina.
Figs 1-8 in Two new Japanagromyza Sasakawa (Diptera: Agromyzidae) from Brazil
Figs 1-8. Japanagromyza arcuaria sp. nov.: 1, adult male, lateral view; 2, adult female, lateral view; 3, epandrium; phallus: 4, lateral view; 5, ventral view; 6, ejaculatory apodeme; 7, oviscape; 8, spermathecae.
Figs 9-12 in Two new Japanagromyza Sasakawa (Diptera: Agromyzidae) from Brazil
Figs 9-12. Japanagromyza chapadensis sp. nov.: 9, adult male lateral view; 10, phallus lateral view; 11, phallus ventral view; 12, ejaculatory apodeme.
Fig.14 in Molecular and morphological approaches for species delimitation and hybridization investigations of two Cichla species
Fig.14. Cluster similarity based on the meristic data of Cichla Bloch & Schneider, 1801 specimens, indicating the relationship among Cichla kelberi Kullander & Ferreira, 2006, Cichla piquiti Kullander & Ferreira, 2006 and carijó samples.
Figs 9-12. Fig. 9 in Molecular and morphological approaches for species delimitation and hybridization investigations of two Cichla species
Figs 9-12. Fig. 9, patterns of PCR-multiplex for the COI mitochondrial gene. Fig. 10, PCR-RFLP patterns of the COI gene with NlaIV enzymes. Fig. 11, patterns of PCR-multiplex for the RAG nuclear gene. Fig. 12, PCR-RFLP patterns of the RAG gene with the BsrI enzyme. The species are indicated as: column 1, Cichla kelberi Kullander & Ferreira, 2006; column 2, Cichla piquiti Kullander & Ferreira, 2006; column 3 and 4, Cichla kelberi; column 5 and 6, Cichla piquiti; column 7 and 8, carijó; M, 1 kb molecular weight marker.
Fig. 8 in Molecular and morphological approaches for species delimitation and hybridization investigations of two Cichla species
Fig. 8. Restriction maps of the COI gene and RAG1 gene for the species Cichla kelberi Kullander & Ferreira, 2006 and Cichla piquiti Kullander & Ferreira, 2006.
Fig. 13 in Molecular and morphological approaches for species delimitation and hybridization investigations of two Cichla species
Fig. 13. Principal Component Analysis (PCA) for Cichla Bloch & Schneider, 1801 specimens using morphological data. Highlight: Cichla kelberi Kullander & Ferreira, 2006, Cichla piquiti Kullander & Ferreira, 2006 and carijó samples distribution.
Figs 4-6. Fig. 4 in Molecular and morphological approaches for species delimitation and hybridization investigations of two Cichla species
Figs 4-6. Fig. 4: Cichla kelberi Kullander & Ferreira, 2006; Fig. 5: Cichla piquiti Kullander & Ferreira, 2006; Fig. 6: carijó.
Fig. 7 in Molecular and morphological approaches for species delimitation and hybridization investigations of two Cichla species
Fig. 7. Recognition and orientation sites of universal and species-specific primers within regions of the mitochondrial (COI) and nuclear (RAG1) genes of Cichla Bloch & Schneider, 1801 species.
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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.