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LOTOS files for Local earthquake tomography of the Aegean crust: Implications for active deformation, large earthquakes, and arc volcanism
<p>This archive contains LOTOS codes and model files/folders associated with the publication "Local earthquake tomography of the Aegean crust: Implications for active deformation, large earthquakes, and arc volcanism" (inside Aeg_tomo.zip)</p> <p> </p> <p>New in version 2:</p> <p>3D model files as well as lateral sections for Vp, Vs, and Vp/Vs (inside nc_3d_model.zip)</p>
Data from: foraging and the importance of knowledge in Pemba, Tanzania: implications for childhood evolution
<p>Childhood is a period of life unique to humans. Childhood may have evolved through the need to acquire knowledge and subsistence skills. In an effort to understand the functional significance of childhood, previous research examined increases with age in returns to foraging across food resources. Such increases could be due to changes in knowledge, or other factors such as body size or strength. Here we attempt to unpack these age-related changes. First we estimate age-specific foraging returns for two resources. We then develop non-linear structural equation models to evaluate the relative importance of ecological knowledge, grip strength, and height in a population of part-time children foragers on Pemba island, Tanzania. We use anthropometric measures, estimates of ecological knowledge, and behavioral observations for 63 individuals across 370 foraging trips. We find slower increases in foraging returns with age for trap hunting than for shellfish collection. We do not detect any effect of individual knowledge on foraging returns, potentially linked to information-sharing within foraging parties. Producing accurate estimates of the distinct contribution of specific traits to an individual's foraging performance constitutes a key step in evaluating different hypotheses for the emergence of childhood.</p>
Zebra finches increase social behavior in traffic noise: implications for urban songbirds
<p>Statistical code & datasets for "Zebra finches increase social behavior in traffic noise: implications for urban songbirds" manuscript submitted to <em>Acta ethologica. </em>Also includes audio file for traffic noise playback in described experiment. </p>
Fig. 5 in Bird Diversity Differs Between Industrial Tree Plantations On Borneo: Implications For Conservation Planning
Fig. 5. Nonlinear multidimensional scaling of bird survey data pooled by point-transect. Vectors represent correlations between the ordination and habitat variables. Vectors and Pearson correlation coefficients are plotted for habitat variables with an r2> 0.200 for axis 1.
Fig. 4 in Bird Diversity Differs Between Industrial Tree Plantations On Borneo: Implications For Conservation Planning
Fig. 4. Plots of (A) species and (B) individual rates (from Fig. 1) versus number of species listed by www.birdlife.org (Table 1) per habitat type.
Fig. 1 in Bird Diversity Differs Between Industrial Tree Plantations On Borneo: Implications For Conservation Planning
Fig. 1. Map of forest occurrence in Borneo in 2005 (WWF-Malaysia, 2005) showing the localities of the Sarawak Planted Forest Project and Sabah Softwoods plantation.
FIG. 9 in Charophyte flora from the Miocene of Zahle (Beeka Valley, Lebanon). Biostratigraphic, palaeoenvironmental and palaeobiogeographical implications
FIG. 9. — Neogene chronostratigraphy. Suggested age of the base of the lacustrine deposits of Zahle according to the charophyte assemblage. European charophyte biozonations and distribution of species are after Riveline et al. (1996).
FIGURE 10 in A new collared lizard (Tropidurus: Tropiduridae) endemic to the Western Bolivian Andes and its implications for seasonally dry tropical forests
FIGURE 10. Scatterplots of PC1 and PC2 generated by the principal component analyses and LD1 and LD2 generated by the linear discriminant analyses performed on meristic variables (scale counts). See table 7 for corresponding summary statistics. Figure color-coded following species labels in figure 11.
FIGURE 8 in A new collared lizard (Tropidurus: Tropiduridae) endemic to the Western Bolivian Andes and its implications for seasonally dry tropical forests
FIGURE 8. Boxplots showing variation in scale counts among Tropidurus chromatops, T. etheridgei, and T. azurduyae.
FIGURE 7 in A new collared lizard (Tropidurus: Tropiduridae) endemic to the Western Bolivian Andes and its implications for seasonally dry tropical forests
FIGURE 7. Scatterplots of PC1 and PC2 generated by the principal component analyses and LD1 and LD2 generated by the linear discriminant analyses performed on morphometric variables. See table 4 for corresponding summary statistics. Figure color-coded following species labels in figure 11.
FIGURE 6 in A new collared lizard (Tropidurus: Tropiduridae) endemic to the Western Bolivian Andes and its implications for seasonally dry tropical forests
FIGURE 6. Live specimens of Tropidurus chromatops Harvey and Gutberlet, 1998 from isolated granitic outcrops ~30 km W Florida, Santa Cruz, Bolivia (14° 36′ 17.28″ S, 61° 29′ 32.64″ W — WGS84 system; ~309 m). A, C, Adult female (MHNC-R 3003). B, D, Adult male (MHNC-R 3018).
FIGURE 5 in A new collared lizard (Tropidurus: Tropiduridae) endemic to the Western Bolivian Andes and its implications for seasonally dry tropical forests
FIGURE 5. Adult male of Tropidurus chromatops Harvey and Gutberlet, 1998 (MHNC-R 3018), illustrating the expanded lateral neck mite pockets and the colorful facial mask with touches of blue and cream, characteristic of the species.
FIGURE 4 in A new collared lizard (Tropidurus: Tropiduridae) endemic to the Western Bolivian Andes and its implications for seasonally dry tropical forests
FIGURE 4. Preserved holotype of Tropidurus azurduyae (adult male, MHNC-R 3011). A, Dorsal head. B, Ventral head. C, Lateral head. D, Ventral body. E, Lateral body. F, Dorsal body.
FIGURE 3 in A new collared lizard (Tropidurus: Tropiduridae) endemic to the Western Bolivian Andes and its implications for seasonally dry tropical forests
FIGURE 3. Live specimens of Tropidurus etheridgei Cei, 1982 and T. azurduyae. A, C, Adult male of T. etheridgei (AMNH-R 176273) from Orloff, Colonia 15, Filadelfia, Boquerón, Paraguay (22° 19′ 58.42″ S, 59° 55′ 00.02″ W — WGS84 system; ~136 m). B, D, Adult female of T. etheridgei (AMNH-R 176277) from Estancia Esmeraldas, Boquerón, Paraguay (20° 59′ 15.81″ S 61° 59′ 27.90″ W — WGS84 system; ~329 m). E, G, Adult female (allotype MHNC-R 3009) of T. azurduyae. F, H, Adult male (holotype MHNC-R 3011) of T. azurduyae.
FIGURE 1 in A new collared lizard (Tropidurus: Tropiduridae) endemic to the Western Bolivian Andes and its implications for seasonally dry tropical forests
FIGURE 1. Habitats visited in the Torotoro National Park, Potosí, Bolivia. A–D, Prepuna (18° 7′ 10.92″ S, 65° 48′ 30.24″ W — WGS84 system; ~2798 m). E–G, Inter-Andean dry valleys at the type locality of Tropidurus azurduyae (18° 5′ 54.24″ S, 65° 44′ 57.48″ W — WGS84 system; ~2264 m). H, Adult male of T. azurduyae, sighted (not collected) at the type locality of the species.
Text-fig. 9. Phylogenetic tree indicating the number of required character state changes (steps) under parsimony for various positions of Miranthus gen. nov. in a molecular based backbone tree (see material and methods for additional details). in Early Flowers Of Primuloid Ericales From The Late Cretaceous Of Portugal And Their Ecological And Phytogeographic Implications
Text-fig. 9. Phylogenetic tree indicating the number of required character state changes (steps) under parsimony for various positions of Miranthus gen. nov. in a molecular based backbone tree (see material and methods for additional details).
Characterizing juvenile dispersal dynamics of invasive barred owls: implications for management
<p>Characterizing natal dispersal can help manage the spread of invasive species expanding their ranges in response to land use and climate change. The Barred Owl (<em>Strix varia</em>) is a prominent example of an apex predator undergoing a rapid range expansion, having spread from eastern to western North America where it is now hyperabundant—threatening the Northern Spotted Owl (<em>S. occidentalis caurina</em>) with extinction and potentially endangering many other native species. We attached satellite tags to 31 Barred Owl juveniles at the southern leading edge of the Barred Owl's expanding range in California to characterize natal dispersal patterns and inform management. Juveniles traveled up to 100km from natal territories and experienced high mortality (annual survival = 0.204). At landscape scales, juveniles preferentially used forests, shrublands, and lower elevations during dispersal and avoided grasslands and burned areas. At finer scales, juveniles preferred shorter (younger) forests, lower elevations, and drainages, and avoided unforested areas. Our results suggest the Barred Owl range expansion is being driven primarily by high reproductive rates and densities despite low juvenile survival rates and dispersal through putatively suboptimal younger forests as a result of exclusion from high-quality habitat by territorial individuals. These findings also point to several strategies for conserving Spotted Owls and other native species in the Barred Owl's expanded range, including: (1) creating and maintaining Barred Owl-free reserves bounded by open or high-elevation areas; (2) creating reserves large enough to reduce immigration by long distance dispersers; and (3) removing Barred Owls from large riparian corridors. </p>
Figure 1 in Establishment of Sinoxylon anale Lesne (Coleoptera: Bostrichidae) in Brazil and its potential implications
Figure 1. Distribution of Sinoxylon anale field collections in Brazil. WP – collection associated with wood pallets from India (Teixeira et al. 2002), ES – collection at pallet heat-treatment facility in the state of Espírito Santo, and PR – collection in a Toona ciliata stand in the state of Paraná, and SP – collection in a natural forest stand in state of São Paulo.
Figure 12 in The anatomy of Odobenocetops (Delphinoidea, Mammalia), the walrus-like dolphin from the Pliocene of Peru and its palaeobiological implications
Figure 12. Odobenocetops leptodon, referred specimen (MNHN SAO 202). Left forelimb in lateral (A) and medial (B) views.
Figure 5 in The anatomy of Odobenocetops (Delphinoidea, Mammalia), the walrus-like dolphin from the Pliocene of Peru and its palaeobiological implications
Figure 5. Reconstruction of the dorsal view of the rostrum of Odobenocetops leptodon. Abbreviations: Fps, fossa for the premaxillary sac; Fr, frontal; Mx, maxilla; NaF, narial fossa; Pmx, premaxilla; Sb, supplementary bone.
ScienceDex guides
Understand access before you commit
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)
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.