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FIGURE 4 in Spintherobolus papilliferus in the rio Ribeira de Iguape basin: implications for the biogeography and conservation of an endangered species (Ostariophysi: Characiformes)
FIGURE 4 | Maximum likelihood tree of species of Spintherobolus based on partial sequences of the COI gene (531 bp). Numbers represent voucher specimens deposited in LBP (Tab. 1). Vouchers LBP 101792 and 101793 are from rio Ribeira de Iguape drainage, municipality of Juquitiba, and voucher LBP 61600 is from rio Sertãozinho, rio Itapanhaú drainage, municipality of Bertioga, both São Paulo State, Brazil.
FIGURE 3 in Spintherobolus papilliferus in the rio Ribeira de Iguape basin: implications for the biogeography and conservation of an endangered species (Ostariophysi: Characiformes)
FIGURE 3 | A. Boxplot for dependent variables body depth (BD), predorsal distance (PD), preanal distance (PA), caudal-peduncle depth (CPD), and upper jaw length (UJL) of Spintherobolus papilliferus from the three drainages: Itapanhaú (IT), Ribeira de Iguape (RI), and upper rio Tietê (UT). B. Scatter plot of LDA features for distinct drainages Itapanhaú (IT – red dots), Ribeira de Iguape (RI – green dots), and upper rio Tietê (UT – blue dots).
FIGURE 5 in Spintherobolus papilliferus in the rio Ribeira de Iguape basin: implications for the biogeography and conservation of an endangered species (Ostariophysi: Characiformes)
FIGURE 5 | Map of southeastern South America showing a detail of the map of São Paulo State (dark grey in small map) and the three drainages discussed in this study: upper rio Tietê (yellow), rio Itapanhaú (pink) and rio Ribeira de Iguape (green). Localities 1–4 belong to the upper rio Tietê, locality 5 belongs to rio Itapanhaú and locality 6 belongs to rio Juquiá, rio Ribeira de Iguape drainages. PE = Parque Estadual.
FIGURE 2 in Spintherobolus papilliferus in the rio Ribeira de Iguape basin: implications for the biogeography and conservation of an endangered species (Ostariophysi: Characiformes)
FIGURE 2 | Stream stretch affluent of rio Juquiá, rio Ribeira de Iguape, municipality of Juquitiba, São Paulo State, where specimens of Spintherobolus papilliferus were sampled for this study. A. General view showing rapids in the background. B. Rapids pool where specimens were caught.
FIGURE 1 in Spintherobolus papilliferus in the rio Ribeira de Iguape basin: implications for the biogeography and conservation of an endangered species (Ostariophysi: Characiformes)
FIGURE 1 | Spintherobolus papilliferus sampled in an affluent of rio Juquiá, rio Ribeira de Iguape drainage, municipality of Juquitiba, São Paulo State, Brazil. A. Live specimen right after capture. B. LISO 426, fixed specimen, 33.0 mm SL. Scale bar = 10 mm.
Fig. 4 in A new gobiconodontid mammal from the Early Cretaceous of Spain and its palaeogeographic implications
Fig. 4. Gobiconodontidae indet. SEM micrographs of the distal cingulum and the enamel at the occlusal view of the broken cusp B of the upper molariform M3, 4 MPZ 2002/73 (Vallipón, Teruel, Spain, upper Barremian) in occlusal view, mesial side is down (A), detail of distal cingular cuspule (B), dentine layers at the anterior broken part of the tooth and enamel cover detailed in D (C), a detail of the enamel ultrastructure showing the radial type of the enamel prisms (D).
Fig. 3 in A new gobiconodontid mammal from the Early Cretaceous of Spain and its palaeogeographic implications
Fig. 3. Gobiconodontidae indet. Stereo SEM micrographs of the occlusal view of the upper molariform M3 or M4, MPZ 2002/73 (Vallipón, Teruel, Spain, upper Barremian). The mesial side is up.
Fig. 2 in A new gobiconodontid mammal from the Early Cretaceous of Spain and its palaeogeographic implications
Fig. 2. Gobiconodontidae indet. SEM micrographs of the upper molariform M3 or M4 MPZ 2002/73 (Vallipón, Teruel, Spain, upper Barremian) in lingual (A), occlusal (B), posterior (C), labial (D), and anterior (E) views. White line in A shows the distal cingulum and the direction of tooth wear made possibly by cusp a of the corresponding lower molariform. In B, mesial is up, the arrows on the left show the lingual cingulum, the arrow at the bottom the distal cingulum. In E the arrow shows the pulp cavity.
Fig. 1 in A new gobiconodontid mammal from the Early Cretaceous of Spain and its palaeogeographic implications
Fig. 1. Geographical and geological situation of the Vallipón site (upper Barremian, Teruel, Spain).
Fig. 6 in A new gobiconodontid mammal from the Early Cretaceous of Spain and its palaeogeographic implications
Fig. 6. Palaeogeography of the Hauterivian (sensu Smith et al., in Martill and Naish, 2001). Abbreviations: 1, Vallipón (upper Barremian, Spain); 2, Cloverly (Aptian–Albian, USA); 3, Shestakovo (Albian, Siberia); 4, Oshih (Hauterivian, Gobi, China), Ejinhoro (Barremian, Gobi, China), Khoboor (Albian, Gobi, Mongolia), Mazongshan (Albian, Gansu, China); 5, Lujiatum Beds, Yixian Formation (Hauterivian, Liaoning, China).
Fig. 5 in A new gobiconodontid mammal from the Early Cretaceous of Spain and its palaeogeographic implications
Fig. 5. Stratigraphical distribution of the gobiconodontid record. The age and order of the localities and formations were established basing on Ostrom (1970), Lucas and Estep (1998), Averianov and Skutchas (2000), and Zhou et al. (2003).
Fig. 14 in Late Miocene large mammals from Yulafli, Thrace region, Turkey, and their biogeographic implications
Fig. 14. Map (slightly modified from Vasiliev et al. 2004) of the Tethys (dark grey) and Paratethys (light grey) region in early late Miocene times, showing the main mammalian localities with and without Dorcatherium, and the tentative extent of the provinces discussed in the text. 1, North−Western Province; 2, North−Dacian Province; 3, Balkano−Iranian (= Sub−Paratethyan) Province; 4, Greek Macedonian Province; 5, Eastern Aegean Province; 6, Anatolian Province.
Fig. 13 in Late Miocene large mammals from Yulafli, Thrace region, Turkey, and their biogeographic implications
Fig. 13. Plot of length vs. distal width of the metacarpal of some large late Miocene Giraffidae. Black symbols are for "Palaeogiraffa", others are for Samotherium.
Fig. 9 in Late Miocene large mammals from Yulafli, Thrace region, Turkey, and their biogeographic implications
Fig. 9. Measurements of the cross−section of the lower i2s in various Proboscideans. From Tassy (1986: fig. 14) and y = Yulafll.
Fig. 2 in Late Miocene large mammals from Yulafli, Thrace region, Turkey, and their biogeographic implications
Fig. 2. Indarctos arctoides, TTMEU−CY−46, Yulafli, Turkey, Vallesian, late Miocene. Left mandibular ramus, lateral (A) and occlusal (B) views of p2–m2 (stereo).
Figure 1 in The effect of photobleaching on bee (Hymenoptera: Apoidea) setae color and its implications for studying aging and behavior
Figure 1. Unstandardized color photographs of the dorsal view of a worker of Bombus huntii Greene. The square box demarcates the lateral distal region of terga 2 and 3 where setal color was sampled for the 'before' and 'after' comparisons in the control and sun-exposed treatments.
Figure 2 in The effect of photobleaching on bee (Hymenoptera: Apoidea) setae color and its implications for studying aging and behavior
Figure 2. Data distributions of 'before' and 'after' measurements of setal color on the lateral distal region of the terga 2 and 3 for the control and sun-exposed treatments. Setal color was measured using the color property hue (H). Letters above each boxplot correspond to a significant difference between treatments of at least 0.05 based on Tukey's adjusted multiple comparison tests.
Figure 3 in The effect of photobleaching on bee (Hymenoptera: Apoidea) setae color and its implications for studying aging and behavior
Figure 3. Correlation (τ) between wing wear (W) and setal color (hue, H) of three bee species: Bombus huntii Greene, Melecta pacifica fulvida Cresson, and Osmia integra Cresson. Larger H values represent increased photobleaching of setae, whereas smaller values of H represent less photobleaching of setae. Larger W represents increased wing wear, whereas smaller W represents decreased wing wear.
Figure 12 in The anatomy of the thyroid gland among "fishes": phylogenetic implications for the Vertebrata
Figure 12. - Distribution of the thyroidian patterns in Acanthomorphs. The interrelationship tree have been reconstructed from Li (2008), and Betancur- R et al. (2013b). See text and Appendix I for details.
Figure 11 in The anatomy of the thyroid gland among "fishes": phylogenetic implications for the Vertebrata
Figure 11. - Distribution of the thyroidian patterns in Teleostei. The interrelationship tree has been reconstructed from Li (2008), Broughton (2010) and Betancur-R et al. (2013b). See text and Appendix I for 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.
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.