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Fig. 3 in Feeding habits and morphometry of Iheringichthys labrosus (Lütken, 1874) in the Uruguay River (Uruguay)
Fig. 3. Correspondence analysis between prey items (circles) and fish size ranges (squares), 1 and 2. Note that the analysis resolved in only one dimension.
Fig. 3 in Habitat partitioning, habits and convergence among coastal nektonic fish species from the São Sebastião Channel, southeastern Brazil
Fig. 3. Dendrogram of ecomorphological relationships (similarity) for the 17 nektonic fish species studied. Cluster analysis is by the Euclidean distance measure and Group Average linkage method using the same scores (i.e., coordinates) calculated for PCA and plotted in Fig. 2 (cophenetic coefficient r = 0.86). Anc tri = Anchoa tricolor; Ath bra = Atherinella brasiliensis; Car lat = Caranx latus; Chl chr = Chloroscombrus chrysurus; Fis tab = Fistularia tabacaria; Har jag = Harengula jaguana; Hyp uni = Hyporhamphus unifasciatus; Lag lae = Lagocephalus laevigatus; Mug cur = Mugil curema; Oli sau = Oligoplites saurus; Pom sal = Pomatomus saltatrix; Sar jan = Sardinella janeiro; Sco bra = Scomberomorus brasiliensis; Sel vom = Selene vomer; Str tim = Strongylura timucu; Tra car = Trachinotus carolinus; Tri lep = Trichiurus lepturus. There is no scale among the fishes (see Table 2 for standard length range) (illustrations: Alexandre C. Ribeiro).
Fig. 2 in Habitat partitioning, habits and convergence among coastal nektonic fish species from the São Sebastião Channel, southeastern Brazil
Fig. 2. Distribution of the 17 nektonic fish species in ecomorphological space. Ordination is by the first two axes of PCA (cumulative % of variance = 73) (see Table 5). Anc tri = Anchoa tricolor; Ath bra = Atherinella brasiliensis; Car lat = Caranx latus; Chl chr = Chloroscombrus chrysurus; Fis tab = Fistularia tabacaria; Har jag = Harengula jaguana; Hyp uni = Hyporhamphus unifasciatus; Lag lae = Lagocephalus laevigatus; Mug cur = Mugil curema; Oli sau = Oligoplites saurus; Pom sal = Pomatomus saltatrix; Sar jan = Sardinella janeiro; Sco bra = Scomberomorus brasiliensis; Sel vom = Selene vomer; Str tim = Strongylura timucu; Tra car = Trachinotus carolinus; Tri lep = Trichiurus lepturus. There is no scale among the fishes (see Table 2 for standard length range) (illustrations: Alexandre C. Ribeiro).
Fig. 1 in Habitat partitioning, habits and convergence among coastal nektonic fish species from the São Sebastião Channel, southeastern Brazil
Fig. 1. Map indicating the location of the study area (São Sebastião Channel) and the marine station of the University of São Paulo (CEBIMar-USP) on the coast of São Paulo, southeastern Brazil.
Fig. 5 in Temporal and ontogenetic variations in feeding habits of Hollandichthys multifasciatus (Teleostei: Characidae) in coastal Atlantic rainforest streams, southern Brazil
Fig. 5. Proportion of autochthonous and allochthonous food items in the diet of Hollandichthys multifasciatus according to the method proposed by Costello (1990).
Fig. 3 in Temporal and ontogenetic variations in feeding habits of Hollandichthys multifasciatus (Teleostei: Characidae) in coastal Atlantic rainforest streams, southern Brazil
Fig. 3. Monthly distribution of the environmental factors measured pH (a), water temperature (b) and water current (c) in the streams investigated.
Fig. 4 in Temporal and ontogenetic variations in feeding habits of Hollandichthys multifasciatus (Teleostei: Characidae) in coastal Atlantic rainforest streams, southern Brazil
Fig. 4. Monthly variation of the rainfall (mm) in the sample period provided by the Center of Environmental Resources Information and Hydrometeorology of Santa Catarina (Ciram- Epagri).
Fig. 4 in Feeding habits of Thoracocharax stellatus (Characiformes: Gasteropelecidae) in the upper rio Tocantins, Brazil
Fig. 4. Principal Components Analysis plot, based on the volumetric proportions of food items consumed by individuals of Thoracocharax stellatus in the upper rio Tocantins.
Fig. 1 in Feeding habits of Thoracocharax stellatus (Characiformes: Gasteropelecidae) in the upper rio Tocantins, Brazil
Fig. 1. Location of the study area, in the upper Rio Tocantins, where the Serra da Mesa Hydroelectric Dam was installed – Estado de Goiás, central Brazil.
Fig. 3 in Feeding habits of Thoracocharax stellatus (Characiformes: Gasteropelecidae) in the upper rio Tocantins, Brazil
Fig. 3. Representation of the alimentary index (IAi), associating relative frequency (FO%), and relative volume (VO%) of the main items in the diet of Thoracocharax stellatus of the upper rio Tocantins.
Fig. 2 in Feeding habits of Thoracocharax stellatus (Characiformes: Gasteropelecidae) in the upper rio Tocantins, Brazil
Fig. 2. Voucher specimen of Thoracocharax stellatus (5.54 cm in standard length) from the upper rio Tocantins (MNRJ 17659).
Figure 9. A in Cranial morphology and dietary habits of rodents
Figure 9. A, log-log plot of the square root of cheek tooth area (√TA) vs. centroid size (dorsal), regression line: y = -1.220 + 1.216x, standard error of the estimate = 0.088, correlation coefficient r = 0.945, dashed reference line represents isometric scaling: y = -1.220 + x. B, plot of relative cheek tooth area [(√TA)/skull length] versus first canonical variate scores. Individual points represent species averages. Numbers associated with each point identify individual species in Appendix 1.
Figure 1 in Cranial morphology and dietary habits of rodents
Figure 1. Landmarks indicated on: A, dorsal, B, left lateral, and C, ventral views of the skull of Castor canadensis. Definitions of landmarks are included in Table 3.
Figure 8 in Cranial morphology and dietary habits of rodents
Figure 8. Box plots of incisor shape for dietary categories. A, incisor anteroposterior (AP) diameter divided by transverse (T) diameter. B, incisor procumbency angle. Bars display the mean, boxes represent the standard deviation, and whiskers represent the extreme values for each dietary group. Numbers associated with outliers identify individual species in Appendix 1.
Figure 10 in Cranial morphology and dietary habits of rodents
Figure 10. Skulls of selected members of the Muridae, illustrating some differences in cranial and dental structure associated with different diets. Each skull is scaled to the same total length. Scale bars with each skull represent 10 mm.
Figure 2. A in Cranial morphology and dietary habits of rodents
Figure 2. A, linear, and B, angular measurements illustrated on the skull of Castor canadensis. Note: although measurements are only illustrated for P4, all premolars and molars were measured.
Figure 7 in Cranial morphology and dietary habits of rodents
Figure 7. Plot of first (CV1) and second (CV2) canonical variates; included are thin-plate splines for maximum observed deformations in each of the three views of the skull along each canonical axis. This figure is identical to Fig. 5 except that extinct rodent taxa with inferred diets are also included. Individual points represent the average shape for each species. Numbers associated with each point identify individual species in Appendix 1.
Figure 3 in Cranial morphology and dietary habits of rodents
Figure 3. Relative warp plots for the dorsal, lateral, and ventral views of the skull. A, first (DRW1) and third (DRW3) dorsal relative warps, B, first (LRW1) and fourth (LRW4) lateral relative warps, C, first (VRW1) and second (VRW2) ventral relative warps. Individual points represent the average shape for each species. Numbers associated with each point identify individual species in Appendix 1. Shape deformations associated with each axis are illustrated in Fig. 4.
Figure 6 in Cranial morphology and dietary habits of rodents
Figure 6. Plot of first (CV1) and third (CV3) canonical variates; included are thin-plate splines for maximum observed deformations in each of the three views of the skull along each canonical axis. Individual points represent the average shape for each species. Numbers associated with each point identify individual species in Appendix 1.
Figure 5 in Cranial morphology and dietary habits of rodents
Figure 5. Plot of first (CV1) and second (CV2) canonical variates; included are thin-plate splines for maximum observed deformations in each of the three views of the skull along each canonical axis. Individual points represent the average shape for each species. Numbers associated with each point identify individual species in Appendix 1.
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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
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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.