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100 results for “Armadillo”
FIGURE 6 in Reassessment of the hairy long-nosed armadillo " Dasypus " pilosus (Xenarthra, Dasypodidae) and revalidation of the genus Cryptophractus Fitzinger, 1856
FIGURE 6. Skull of Cryptophractus pilosus (MUSM 7501) in dorsal (A), ventral (B), and lateral (C) views, and right mandibular ramus (MUSM 7502) in lateral view (D). Scale bars equal 10 mm.
FIGURE 2 in Reassessment of the hairy long-nosed armadillo " Dasypus " pilosus (Xenarthra, Dasypodidae) and revalidation of the genus Cryptophractus Fitzinger, 1856
FIGURE 2. Most parsimonious tree resulting from the cladistic analysis of 58 characters (tree length = 113; Consistency Index = 0.66, Retention Index = 0.61). Capital letters represent the nodes discussed in the text; sinapomorphies given below the nodes and autapomorphies given along each branch, following the numbers assigned in Appendix 2.
FIGURE 8 in Reassessment of the hairy long-nosed armadillo " Dasypus " pilosus (Xenarthra, Dasypodidae) and revalidation of the genus Cryptophractus Fitzinger, 1856
FIGURE 8. Comparison of the postcranial elements of Cryptophractus pilosus and Dasypus novemcinctus, which is represented by ('). (A), lumbar vertebrae; (B), sinsacrum; (C), femur; (D), tibia-fibula; (E), astragalus; and (F), calcaneum. Scale bars equal 10 mm.
Figure 9 in Redescription of the terrestrial isopod Armadillo mayeti Simon, 1885 and its comparison with Armadillo officinalis Duméril, 1816 from Tunisian populations
Figure 9. Male Armadillo officinalis. (A) Telson with uropods, dorsal view. (B) Uropod exopodite insertion, dorsal view. (C) Pleopod 2. (D) Pleopod 1.
Figure 5 in Redescription of the terrestrial isopod Armadillo mayeti Simon, 1885 and its comparison with Armadillo officinalis Duméril, 1816 from Tunisian populations
Figure 5. Male Armadillo mayeti. (A) Pereopod 1. (B) Pereopod 7. (C) Exopodite pleopod 1. (D) Endopodite pleopod 1. (E) Pleopod 2.
Figure 6 in Redescription of the terrestrial isopod Armadillo mayeti Simon, 1885 and its comparison with Armadillo officinalis Duméril, 1816 from Tunisian populations
Figure 6. Male Armadillo mayeti. (A) Stridulation apparatus on propodus 5. (B) Enlarged scale. (C) Scale-setae on tergite I enlarged scale.
Figure 2 in Redescription of the terrestrial isopod Armadillo mayeti Simon, 1885 and its comparison with Armadillo officinalis Duméril, 1816 from Tunisian populations
Figure 2. Male Armadillo mayeti. (A) Cephalon and tergite I dorsal view with numerous setae. (B) Pereonite I and II with lateral groove. (C) Pleotelson ventral view (pereopods 7 removed) with bilobed caudal process, pereopods 6, pleopods 1 and 2, uropods, telson apex.
Figure 4 in Redescription of the terrestrial isopod Armadillo mayeti Simon, 1885 and its comparison with Armadillo officinalis Duméril, 1816 from Tunisian populations
Figure 4. Male Armadillo mayeti. (A) Right mandible. (B) Left mandible. (C) Maxilliped. (D) Maxillula. (E) Maxilla.
Figure 8 in Redescription of the terrestrial isopod Armadillo mayeti Simon, 1885 and its comparison with Armadillo officinalis Duméril, 1816 from Tunisian populations
Figure 8. Male Armadillo officinalis. (A) Antenna. (B) Pereopod 1. (C) Pereopod 7. (D) Uropod, ventral view.
Figure 7 in Redescription of the terrestrial isopod Armadillo mayeti Simon, 1885 and its comparison with Armadillo officinalis Duméril, 1816 from Tunisian populations
Figure 7. Male Armadillo officinalis. (A) Body, lateral view. (B) Pereion-epimera I and II latero-ventral view. (C) Cephalon and tergite I, dorsal view. (D) Setae on tergite I. (E) Pleotelson ventral view (pereopods 7 removed) with pereopods 6, pleopods l and 2, uropods, telson apex. (F) Stridulation apparatus on propodus 5. (G) Enlarged scale.
Figure 3 in Redescription of the terrestrial isopod Armadillo mayeti Simon, 1885 and its comparison with Armadillo officinalis Duméril, 1816 from Tunisian populations
Figure 3. Male Armadillo mayeti. (A) Antenna. (B) Antennula. (C) Telson dorsal view. (D) Uropod exopodite insertion. (E) Uropod ventral view.
On following pages: 3. Large Hairy Armadillo (Chaetophractus villosus); 4. Pichi (Zaedyus pichiy); 5. Pink Fairy Armadillo (Priodontes maximus): 8. Northern Naked-tailed Armadillo (Cabassous centralis); 9. Southern Naked-tailed Armadillo Armadillo (Cabassous chacoensis); 12. Brazilian Three-banded Armadillo (Tolypeutestricinctus); 13. Southern Three-banded (Chlamyphorus truncatus); 6. Greater Fairy Armadillo (Calyptophractus retusus); 7. Giant Armadillo (Cabassous unicinctus); 10. Greater Naked-tailed Armadillo (Cabassous tatouay); 11. Chacoan Naked-tailed Armadillo (Tolypeutes matacus). in Chlamyphoridae
On following pages: 3. Large Hairy Armadillo (Chaetophractus villosus); 4. Pichi (Zaedyus pichiy); 5. Pink Fairy Armadillo (Priodontes maximus): 8. Northern Naked-tailed Armadillo (Cabassous centralis); 9. Southern Naked-tailed Armadillo Armadillo (Cabassous chacoensis); 12. Brazilian Three-banded Armadillo (Tolypeutestricinctus); 13. Southern Three-banded (Chlamyphorus truncatus); 6. Greater Fairy Armadillo (Calyptophractus retusus); 7. Giant Armadillo (Cabassous unicinctus); 10. Greater Naked-tailed Armadillo (Cabassous tatouay); 11. Chacoan Naked-tailed Armadillo (Tolypeutes matacus).
On following pages: 4. Brazilian Lesser Long-nosed Armadillo (Dasypus septemcinctus); 5. Hairy Long-nosed Armadillo Armadillo (Dasypus hybridus). (Dasypus pilosus); 6. Yungas Lesser Long-nosed Armadillo (Dasypus mazzai); 7. Southern Long-nosed in Dasypodidae
On following pages: 4. Brazilian Lesser Long-nosed Armadillo (Dasypus septemcinctus); 5. Hairy Long-nosed Armadillo Armadillo (Dasypus hybridus). (Dasypus pilosus); 6. Yungas Lesser Long-nosed Armadillo (Dasypus mazzai); 7. Southern Long-nosed
Armadillo detections in Northwest Arkansas
<p>As the human footprint upon the landscape expands, wildlife seeking to avoid human contact are losing the option of altering their spatial distribution and instead are shifting their daily activity patterns to be active at different times than humans. In this study, we used game cameras to evaluate how human development and activity were related to the daily activity patterns of the nine-banded armadillo (<i>Dasypus novemcinctus)</i> along an urban to rural gradient in Arkansas, USA during the winter of 2020-2021. We found that armadillos had substantial behavioral plasticity in regard to the timing of their activity patterns; >95% of armadillo activity was nocturnal at six of the study sites whereas between 30 and 60% of activity occurred during the day at 3 other sites. The likelihood of diurnal armadillo activity was best explained by the distance to downtown Fayetteville (the nearest population center) and estimated ambient sound level (both indices of human activity) with armadillos being most active during the day at quiet sites far from Fayetteville. Furthermore, armadillo activity occurred later during the night period (minutes after sunset)at sites near downtown and with higher anthropogenic sound. Anecdotal evidence suggests that the observed activity shift may be in response to not only human activity but the presence of domestic dogs. Our results provide further evidence that human activity has subtle nonlethal impacts on even common, widespread wildlife species. Because armadillos have low body temperatures and basal metabolism, being active during cold winter nights likely has measurable fitness costs. Nature reserves near human population centers may not serve as safe harbors for wildlife as we intend, and managers could benefit from considering these nonlethal responses in how they manage recreation and visitation in these natural areas.</p>
Figure 4 in Effects of Quaternary climatic oscillations over the Chacoan fauna: phylogeographic patterns in the southern three-banded armadillo Tolypeutes matacus (Cingulata: Chlamyphoridae)
Figure 4. Effective size change over time estimated from BSP analysis corresponding to all the localities for each marker. The y-axis represents the effective size (Ne) expressed on a logarithmic scale. The x-axis represents time in millions of years (Myr) before the present. The dark blue lines represent the median effective population size over time, and the lighter blue areas the range of Ne values with posterior densities higher than 95%. Expansion signals were highlighted in yellow. The analyses for the northern and southern groups are shown in the Supporting Information, Figure S1.
Figure 3 in Effects of Quaternary climatic oscillations over the Chacoan fauna: phylogeographic patterns in the southern three-banded armadillo Tolypeutes matacus (Cingulata: Chlamyphoridae)
Figure 3. Left panel (A) shows groups recovered by Bayesian inference in GENELAND. The middle and right panels present spatial distribution of posterior probability to belong to cluster north (B) and south (C).
Figure 2. Geographic distribution and haplotype networks for 12S in Effects of Quaternary climatic oscillations over the Chacoan fauna: phylogeographic patterns in the southern three-banded armadillo Tolypeutes matacus (Cingulata: Chlamyphoridae)
Figure 2. Geographic distribution and haplotype networks for 12S (top panels) and control region (bottom panels). The panels on the left plot the geographical distribution and frequency of haplotypes in the different localities analysed. Localities were labelled according to their ID (see Table 1). The right panels show the haplotype networks, where the dashes on the lines represent mutations, and the black circles represent intermediate variants not found. Principal Chacoan rivers are shown in light-blue labels. Capitalized labels indicate names of Argentinean provinces, and labels with all letters in uppercase refer to neighbouring countries.
Figure 1 in Effects of Quaternary climatic oscillations over the Chacoan fauna: phylogeographic patterns in the southern three-banded armadillo Tolypeutes matacus (Cingulata: Chlamyphoridae)
Figure 1. Possible range expansion scenarios for Tolypeutes matacus during glacial (A) and interglacial (B) periods. Yellow arrows denote scenarios proposed by Soibelzon (2019), while pink arrows indicate scenarios suggested by results from Ferreiro et al. (2022). Green polygon shows IUCN's current species distribution (Noss et al. 2014), and red and blue dots indicate fossil records from Holocene and Pleistocene periods, respectively (sensu Ferreiro et al. 2022).
Figure 5 in Effects of Quaternary climatic oscillations over the Chacoan fauna: phylogeographic patterns in the southern three-banded armadillo Tolypeutes matacus (Cingulata: Chlamyphoridae)
Figure 5. Spatiotemporal diffusion analysis of lineages for Tolypeutes matacus showing time slices for (A) 1.6 Mya, (B) 1.07 Mya, (C) 580 kya, and (D) the present. Red lines represent branches of the MCC tree and blue-shaded areas: indicate 80% HPD uncertainty in the location of ancestral nodes.
Figure 5. Dasypus hybridus. A in Dental enamel structure in long-nosed armadillos (Xenarthra: Dasypus) and its evolutionary implications
Figure 5. Dasypus hybridus. A, cross-section parallel to the occlusal plane of a permanent molariform. B, C, photomicrographs of the permanent molariform, taken with the scanning electron microscope, showing the enamel layer. Abbreviations: D, dentine; E, enamel; EDJ, enamel–dentine junction; white arrowheads show incremental lines.
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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
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