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3,761 results for “phylogenetic relationship”
Figure 2 in Exploring the phylogenetic landscape: unravelling the relationships and biogeography of the Cosmocerca genus in amphibians
Figure 2. Phylogenetic tree created using the maximum likelihood method based on the internal transcribed spacer (ITS) gene molecular marker of 11 species of cosmocercid nematodes.
Figure 10 in Two new species of the genus Quindina Roewer, 1914 (Opiliones: Nomoclastidae) from Colombia: phylogenetic relationships and notes on their nest architecture
Figure 10. Nest location of Quindina sanantonio sp. n. (A–E) and Quindina horologium sp. n. (F) in leaves. (A) Nest #1; (B) nest #2; (C) nest #3; (D) nest #4; (E) nest #5. Scale bars = 10 mm.
Figure 9 in Two new species of the genus Quindina Roewer, 1914 (Opiliones: Nomoclastidae) from Colombia: phylogenetic relationships and notes on their nest architecture
Figure 9. Nest of Quindina sanantonio sp. n. (A) Close-up of nest #1. (B) Egg with immature harvestmen.
Figure 1 in Two new species of the genus Quindina Roewer, 1914 (Opiliones: Nomoclastidae) from Colombia: phylogenetic relationships and notes on their nest architecture
Figure 1. Quindina sanantonio sp. n. (A–F) Male holotype (MUSENUV-Ar-2240): Habitus in dorsal (A), ventral (B) and lateral (C) views. Female paratype (MUSENUV-Ar-2247): Habitus in dorsal (D), ventral (E) and lateral (F) views. Quindina horologium sp. n: (G–L) Male holotype (MUSENUV-Ar-2229): Habitus in dorsal (G), ventral (H) and lateral (I) views. Female paratype (MUSENUV-Ar-2230): Habitus in dorsal (J), ventral (K) and lateral (L) views. Scale bars = 1 mm.
Figure 5. Topology obtained under K in Two new species of the genus Quindina Roewer, 1914 (Opiliones: Nomoclastidae) from Colombia: phylogenetic relationships and notes on their nest architecture
Figure 5. Topology obtained under K = 7; only the family Nomoclastidae is displayed. Numbers above branches indicate Bootstrap support with absolute frequency (left) and Group present/Contradicted values (right), square brackets indicate negative differences. Navajo rugs: NE, Nelsen strict consensus under equal weighting; K, implied weighting (K 3, 4, 5, 6, 7, 8, 9, 10, 15). Next to each species are depicted the codes for the character #96 (Nest architecture) and a photograph for each state in the box on the right. Nest type 0 photo by Rosanette Quesada.
Figure 4 in Two new species of the genus Quindina Roewer, 1914 (Opiliones: Nomoclastidae) from Colombia: phylogenetic relationships and notes on their nest architecture
Figure 4. Quindina sanantonio sp. n. (A–C) Quindina horologium sp. n. (D–F) Penis in dorsal (A, D), ventral (B, E) and lateral (C, F) views. Abbreviations: A = macrosetae A, C = macrosetae C, E = macrosetae E. Scale bars = 50 mm.
Figure 2 in Two new species of the genus Quindina Roewer, 1914 (Opiliones: Nomoclastidae) from Colombia: phylogenetic relationships and notes on their nest architecture
Figure 2. Quindina sanantonio sp. n. (A–E) Male holotype (MUSENUV-Ar-2240): (A) Habitus, dorsal view; (B) lateral view. (C) Left pedipalp, ventral view, trochanter to tarsus. (D) Leg I, tibia to tarsus in prolateral view. (E) Chelicera (hand, fixed and movable fingers). Scale bars = 1 mm.
Figure 6. Topology obtained under K in Two new species of the genus Quindina Roewer, 1914 (Opiliones: Nomoclastidae) from Colombia: phylogenetic relationships and notes on their nest architecture
Figure 6. Topology obtained under K = 7, with unambiguous character optimisations shown in each branch. Empty and filled hashmarks represent homoplasious and non-homoplasious transformations, respectively, with characters on top and states below. Only the genera Callcosma and Quindina are displayed.
Figure 8 in Two new species of the genus Quindina Roewer, 1914 (Opiliones: Nomoclastidae) from Colombia: phylogenetic relationships and notes on their nest architecture
Figure 8. Nests of Quindina sanantonio sp. n. in the San Antonio Forest, Municipality of Santiago de Cali, Valle del Cauca, Colombia. (A) Nest #1, 29 October 2021. (B) Nest #1, 20 November 2021. (C) Nest #2. (D) Nest #3. (E) Nest #4. (F) Nest #5.
Figure 7 in Two new species of the genus Quindina Roewer, 1914 (Opiliones: Nomoclastidae) from Colombia: phylogenetic relationships and notes on their nest architecture
Figure 7. (A) Trail in San Antonio Forest (Municipality of Santiago de Cali, Valle del Cauca, Colombia). (B–F) Location of Quindina sanantonio sp. n. nests (white arrows) in the San Antonio Forest (B) Nest #1. (C) Nest #2. (D) Nest #3. (E) Nest #4. (F) Nest #5.
Figure 3 in Two new species of the genus Quindina Roewer, 1914 (Opiliones: Nomoclastidae) from Colombia: phylogenetic relationships and notes on their nest architecture
Figure 3. Quindina horologium sp. n. (A–E) Male holotype (MUSENUV-Ar-2229): (A) Habitus, dorsal view; (B) lateral view. (C) Left pedipalp, ventral view, trochanter to tarsus. (D) Leg I, tibia to tarsus in prolateral view. (E) Chelicera (hand, fixed and movable fingers). Scale bars = 1 mm.
Figure 11 in Two new species of the genus Quindina Roewer, 1914 (Opiliones: Nomoclastidae) from Colombia: phylogenetic relationships and notes on their nest architecture
Figure 11. Distribution map of Quindina species in Colombia, including the new species described in this study. The geographical data were taken or georeferenced from Pinto-da-Rocha and Bragagnolo (2017) and Pinzón and Pinto-Da-Rocha (2020).
FIGURE 9 in Biogeographical affinity shapes relationships between ecological and phylogenetic mammal diversity and associations with their environmental correlates in the Americas
FIGURE 9. Non-stationary associations between ecological diversity (ED) and standard deviation in altitude (ALTstd). The maps show the spatial variation in local beta coefficients (b) for ALTstd as predictor of ED, obtained from the full model, i.e., including all environmental predictors and species richness (TR), after application of geographically weighted regression separately on data for each mammal group. Regions of (+) and negative (-) associations are indicated. Maps are in Mollweide equalarea projection. Dash lines on each map indicate the location of the tropics in the Northern and Southern Hemispheres.
FIGURE 5 in Biogeographical affinity shapes relationships between ecological and phylogenetic mammal diversity and associations with their environmental correlates in the Americas
FIGURE 5. Non-stationary associations between ecological diversity (ED) and net primary productivity (NPP). The maps show the spatial variation in local beta coefficients (b) for NPP as predictor of ED, obtained from the full model, i.e., including all environmental predictors and species richness (TR), after application of geographically weighted regression separately on data for each mammal group. Regions of (+) and negative (-) associations are indicated. Maps are in Mollweide equal-area projection. Dash lines on each map indicate the location of the tropics in the Northern and Southern Hemispheres.
FIGURE 4 in Biogeographical affinity shapes relationships between ecological and phylogenetic mammal diversity and associations with their environmental correlates in the Americas
FIGURE 4. Non-stationary associations between ecological diversity (ED) and mean annual temperature (TEMP). The maps show the spatial variation in local beta coefficients (b) for TEMP as predictor of ED, obtained from the full model, i.e., including all environmental predictors and species richness (TR), after application of geographically weighted regression separately on data for each mammal group. Regions of (+) and negative (-) associations are indicated. Maps are in Mollweide equal-area projection. Dash lines on each map indicate the location of tropics in the Northern and Southern Hemispheres.
FIGURE 8 in Biogeographical affinity shapes relationships between ecological and phylogenetic mammal diversity and associations with their environmental correlates in the Americas
FIGURE 8. Non-stationary associations between ecological diversity (ED) and coefficient of variation in annual precipitation (PRECcv). The maps show the spatial variation in local beta coefficients (b) for PRECcv as predictor of ED, obtained from the full model, i.e., including all environmental predictors and species richness (TR), after application of geographically weighted regression separately on data for each mammal group. Regions of (+) and negative (-) associations are indicated. Maps are in Mollweide equal-area projection. Dash lines on each map indicate the location of the tropics in the Northern and Southern Hemispheres.
FIGURE 7 in Biogeographical affinity shapes relationships between ecological and phylogenetic mammal diversity and associations with their environmental correlates in the Americas
FIGURE 7. Non-stationary associations between ecological diversity (ED) and annual range in temperature (TEMPr). The maps show the spatial variation in local beta coefficients (b) for TEMPr as predictor of ED, obtained from the full model, i.e., including all environmental predictors and species richness (TR), after application of geographically weighted regression separately on data for each mammal group. Regions of (+) and negative (-) associations are indicated. Maps are in Mollweide equalarea projection. Dash lines on each map indicate the location of the tropics in the Northern and Southern Hemispheres.
FIGURE 1 in Biogeographical affinity shapes relationships between ecological and phylogenetic mammal diversity and associations with their environmental correlates in the Americas
FIGURE 1. Spatial patterns of variation in the ecological diversity (ED) of different mammal groups over the Americas. Maps are in Mollweide equal-area projection. Dash lines on each map indicate the location of the tropics in the Northern and Southern Hemispheres.
FIGURE 14 in Biogeographical affinity shapes relationships between ecological and phylogenetic mammal diversity and associations with their environmental correlates in the Americas
FIGURE 14. Non-stationary associations between phylogenetic diversity (AvPD) and coefficient of variation in annual precipitation (PRECcv). The maps show the spatial variation in local beta coefficients (b) for PRECcv as predictor of AvPD, obtained from the full model, i.e., including all environmental predictors, after application of geographically weighted regression separately on data for each mammal group. Regions of (+) and negative (-) associations are indicated. Maps are in Mollweide equal-area projection. Dash lines on each map indicate the location of the tropics in the Northern and Southern Hemispheres.
FIGURE 6 in Biogeographical affinity shapes relationships between ecological and phylogenetic mammal diversity and associations with their environmental correlates in the Americas
FIGURE 6. Non-stationary associations between ecological diversity (ED) and annual precipitation (PREC). The maps show the spatial variation in local beta coefficients (b) for PREC as predictor of ED, obtained from the full model, i.e., including all environmental predictors and species richness (TR), after application of geographically weighted regression separately on data for each mammal group. Regions of (+) and negative (-) associations are indicated. Maps are in Mollweide equal-area projection. Dash lines on each map indicate the location of tropics in the Northern and Southern Hemispheres.
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.