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14,185 results for “phylogenies”
Fig. 1 in Phylogeny and Synonymy of Gyrodinium heterostriatum comb. nov. (Dinophyceae), a Common Unarmored Dinoflagellate in the World Oceans
Fig. 1. Map of the sampling stations in the North Sea during the JERICO-NEXT LifeWatch research cruise in May 2019.
Fig. 3 in Molecular Phylogeny of the Sand-dwelling Dinoflagellate Planodinium striatum and Chrysodinium gen. nov. for Plagiodinium ballux (Dinophyceae)
Fig. 3. Line drawings of the plate arrangement of Planodinium striatum (A–C), Plagiodinium belizeanum (D–F) and Chrysodinium ballux gen. nov. & comb. nov. (=Plagiodinium ballux) (G–I). Left lateral (A), right lateral (B), apical (C) views of Planodinium striatum redrawn from Hoppenrath et al. (2014). Left lateral (D), right lateral (E) and apical (F) views of Plagiodinium belizeanum redrawn from Wakeman et al. (2018). Left lateral (G), ventral (H) and apical (I) views of Chrysodinium ballux gen. & comb. nov. redrawn from Yamada et al. (2018) with a re-interpreted tabulation.
Fig. 1 in Molecular Phylogeny of the Sand-dwelling Dinoflagellate Planodinium striatum and Chrysodinium gen. nov. for Plagiodinium ballux (Dinophyceae)
Fig. 1. Light (A–M) and scanning electron microscopy (N–O) images of Planodinium striatum isolated in June 2012 at Wimereux, France. (A–B) A cell in left lateral and dorsal views. Asterisk (*) indicates the pusule. (C–M) Different views of another cell. The arrows indicate hypothecal plates. (N) Cell in ventro-left lateral view. (O) Another cell in left lateral view. The arrowheads indicate the trichocysts. The inset shows a large pore surrounded by several small pores. Scale bar = 10 μm.
Fig. 5 in Jenynsia luxata, a new species from Northwestern Argentina, with additional observations of J. maculata Regan and phylogeny of the genus (Cyprinodontiformes: Anablepidae)
Fig. 5. Topologies from most equally parsimonious trees and relative Bremer support/GC values under (a) equal weights (strict consensus of 12 trees), and (b) implied weighting (strict consensus of two trees), with concavities K = 4 to 20 (with supports measured under K = 8). Unsupported nodes are shown as collapsed. The relationships of genera of the family are consistent with those proposed in previous studies, therefore species of Anableps and Oxyzygonectes are not shown.
Fig. 1 in Jenynsia luxata, a new species from Northwestern Argentina, with additional observations of J. maculata Regan and phylogeny of the genus (Cyprinodontiformes: Anablepidae)
Fig. 1. Jenynsia luxata. Above: holotype CI-FML: 5464, male, 24.4 mm SL, Tucumán, Burruyacu city, a small unnamed stream, río Tajamar basin, Argentina; below: paratype CI-FML 5466, female, 34.8 mm SL, Santiago del Estero, Pellegrini, small flooded pools at Ruta Provincial 4, not connected to but near to río Urueña basin, Argentina.
Fig. 4 in Jenynsia luxata, a new species from Northwestern Argentina, with additional observations of J. maculata Regan and phylogeny of the genus (Cyprinodontiformes: Anablepidae)
Fig. 4. Hydrographic map of South America showing the currently known distribution of Jenynsia luxata. The area delimited by the rectangle is enlarged at right, where the type locality is indicated by an open dot and an additional locality is indicated by a black dot. The small black dot indicates the capital of Tucumán.
Fig. 7 in Phylogenetic relationships of the enigmatic Carlastyanax aurocaudatus (Eigenmann) with remarks on the phylogeny of the Stevardiinae (Teleostei: Characidae)
Fig. 7. Cladogram showing relationships of the Characidae obtained with the Examined Matrix. Node numbers correspond to those cited on the text.
Fig. 4 in Phylogenetic relationships of the enigmatic Carlastyanax aurocaudatus (Eigenmann) with remarks on the phylogeny of the Stevardiinae (Teleostei: Characidae)
Fig. 4. Premaxilla and maxilla of Carlastyanax aurocaudatus, CI-FML 5015, 44.4 mm SL, medial view, anterior to left. Scale bar = 1 mm.
Fig. 3 in Phylogenetic relationships of the enigmatic Carlastyanax aurocaudatus (Eigenmann) with remarks on the phylogeny of the Stevardiinae (Teleostei: Characidae)
Fig. 3. Premaxilla of Carlastyanax aurocaudatus, CI-FML 5015, 44.4 mm SL, ventral view, medial to right. Scale bar = 1 mm.
Fig. 2 in Phylogenetic relationships of the enigmatic Carlastyanax aurocaudatus (Eigenmann) with remarks on the phylogeny of the Stevardiinae (Teleostei: Characidae)
Fig. 2. Lower jaw and part of the suspensorium of Carlastyanax aurocaudatus, CI-FML 5015, 44.4 mm SL, lateral view, anterior to left. Scale bar = 1 mm.
Fig. 6 in Phylogenetic relationships of the enigmatic Carlastyanax aurocaudatus (Eigenmann) with remarks on the phylogeny of the Stevardiinae (Teleostei: Characidae)
Fig. 6. Premaxilla and part of the maxilla of Carlastyanax aurocaudatus, CI-FML 5015, 44.4 mm SL, medial view, anterior to left. Scale bar = 1 mm. Arrow indicates the ligament between middle length of ascendant maxillary process and the premaxilla, described in the character 378.
Fig. 5 in Phylogenetic relationships of the enigmatic Carlastyanax aurocaudatus (Eigenmann) with remarks on the phylogeny of the Stevardiinae (Teleostei: Characidae)
Fig. 5. Cranium and pectoral girdle of Carlastyanax aurocaudatus, CI-FML 5015, 44.4 mm SL, lateral view, anterior to left. Gill skeleton and right suspensorium removed. Scale bar = 5 mm.
Fig. 8 in Phylogenetic relationships of the enigmatic Carlastyanax aurocaudatus (Eigenmann) with remarks on the phylogeny of the Stevardiinae (Teleostei: Characidae)
Fig. 8. Detail of the cladogram obtained with the Extended Matrix. Clade 353 corresponds to the clade with the same number in Fig. 7.
Figure 4 in Morphology, molecular phylogeny and biomass evaluation of Desmodesmus abundans (Scenedesmaceae-Chlorophyceae) from Brazil
Figure 4. Phylogenetic analysis of Desmodesmus species by Bayesian inference using ITS sequences. Posteriori probability values are left from nodes.
Figure 2 in Morphology, molecular phylogeny and biomass evaluation of Desmodesmus abundans (Scenedesmaceae-Chlorophyceae) from Brazil
Figure 2. Lipids and carbohydrate production of D. abundans LGMM0013 andT.obliquus LGMM0001 under autotrophic conditions after 22 days. Bars indicate standard deviation.
Figure 1 in Morphology, molecular phylogeny and biomass evaluation of Desmodesmus abundans (Scenedesmaceae-Chlorophyceae) from Brazil
Figure 1. Growth comparison in autotrophic conditions between D. abundans LGMM0013 and T. obliquus LGMM0001 by dry biomass production. Bars indicate standard deviation.
Fig. 3 in Molecular phylogeny of Indonesian Lymantria Tussock Moths (Lepidoptera: Erebidae) based on CO I gene sequences
Fig. 3. Neighbor-Joining tree based on K2P distance model of all substitutions of CO I gene (Bootstrap support are shown at the nodes; ID=specimens from Indonesia).
Fig. 4. Maximum likelihood tree for 43 in Molecular phylogeny of Indonesian Lymantria Tussock Moths (Lepidoptera: Erebidae) based on CO I gene sequences
Fig. 4. Maximum likelihood tree for 43 species of Lymantria based all substitutions of CO I gene (Bootstrap support are shown at the nodes; ID=specimens from Indonesia).
Figure 9 in The life cycle in late Paleozoic eryopid temnospondyls: developmental variation, plasticity and phylogeny
Figure 9. Phylogenetic relationships within Eryopidae as found in the present analysis, with the most important synapomorphies mapped onto nodes. See Appendix A for character definitions and a matrix, and see the text for a complete list of results.
Figure 8 in The life cycle in late Paleozoic eryopid temnospondyls: developmental variation, plasticity and phylogeny
Figure 8. Morphometrics of eryopiform skulls, depicting crucial skull proportions relative to size. Arrows in (a) highlight ontogeny in O. labyrinthicus and S. haeuseri.
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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)
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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.