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712 results for “Beetle diversity”
Figure 7 from: Zhang M, Ruan Y, Wan X, Tong Y, Yang X, Bai M (2019) Geometric morphometric analysis of the pronotum and elytron in stag beetles: insight into its diversity and evolution. ZooKeys 833: 21-40. https://doi.org/10.3897/zookeys.833.26164
Figure 7 Differences in elytron shape among each branch and ancestor, on the basis of principal component analysis. Empty dots indicate the number of the node on the phylogenetic tree; solid dots indicate the average shape of the extant subfamily/tribe of each branch.
Figure 6 from: Zhang M, Ruan Y, Wan X, Tong Y, Yang X, Bai M (2019) Geometric morphometric analysis of the pronotum and elytron in stag beetles: insight into its diversity and evolution. ZooKeys 833: 21-40. https://doi.org/10.3897/zookeys.833.26164
Figure 6 Differences in pronotum shape among each branch and ancestor, on the basis of principal component analysis. Empty dots indicate the number of the node on the phylogenetic tree; solid dots indicate the average shape of the extant subfamily/tribe of each branch.
Figure 5 from: Zhang M, Ruan Y, Wan X, Tong Y, Yang X, Bai M (2019) Geometric morphometric analysis of the pronotum and elytron in stag beetles: insight into its diversity and evolution. ZooKeys 833: 21-40. https://doi.org/10.3897/zookeys.833.26164
Figure 5 Reconstruction of ancestral groundplans of the elytron in Lucanidae and the outgroups. The splines indicate the deformation of the shapes relative to the reference configuration. The phylogenetic tree was summarized and reconstructed from earlier molecular results (Kim and Farrell 2015).
Figure 3 from: Zhang M, Ruan Y, Wan X, Tong Y, Yang X, Bai M (2019) Geometric morphometric analysis of the pronotum and elytron in stag beetles: insight into its diversity and evolution. ZooKeys 833: 21-40. https://doi.org/10.3897/zookeys.833.26164
Figure 3 Differences in elytron shape between outgroups and Lucanidae, on the basis of principal component analysis at the species level. The four circles are 90%-equal frequency ellipses of Lucanidae subfamilies.
Figure 4 from: Zhang M, Ruan Y, Wan X, Tong Y, Yang X, Bai M (2019) Geometric morphometric analysis of the pronotum and elytron in stag beetles: insight into its diversity and evolution. ZooKeys 833: 21-40. https://doi.org/10.3897/zookeys.833.26164
Figure 4 Reconstruction of ancestral groundplans of the pronotum in Lucanidae and the outgroups. The splines indicate deformation of the shapes relative to the reference configuration. The phylogenetic tree was summarized and reconstructed from earlier molecular results (Kim and Farrell 2015).
Figure 2 from: Zhang M, Ruan Y, Wan X, Tong Y, Yang X, Bai M (2019) Geometric morphometric analysis of the pronotum and elytron in stag beetles: insight into its diversity and evolution. ZooKeys 833: 21-40. https://doi.org/10.3897/zookeys.833.26164
Figure 2 Differences in pronotum shape between outgroups and Lucanidae, on the basis of principal component analysis at the species level. The four circles are 90%-equal frequency ellipses of Lucanidae subfamilies.
Figure 1 from: Zhang M, Ruan Y, Wan X, Tong Y, Yang X, Bai M (2019) Geometric morphometric analysis of the pronotum and elytron in stag beetles: insight into its diversity and evolution. ZooKeys 833: 21-40. https://doi.org/10.3897/zookeys.833.26164
Figure 1 Description of the curves used in geometric morphometric analysis. The positions selected for the pronotum and elytron curves are represented by Prosopocoilus sp. in dorsal view. The curves were resampled in 25 or 50 semi-landmarks (SLM).
Figure 35 from: Staniec B, Pietrykowska-Tudruj E (2019) Pupae of the mega-diverse rove beetle tribe Staphylinini (Coleoptera, Staphylinidae): their traits and systematic significance. ZooKeys 877: 133-159. https://doi.org/10.3897/zookeys.877.35715
Figure 35 Fifty per cent majority rules consensus tree from a maximum parsimony analysis of 22 species of Staphylinini pupae.
Figure 25-34 from: Staniec B, Pietrykowska-Tudruj E (2019) Pupae of the mega-diverse rove beetle tribe Staphylinini (Coleoptera, Staphylinidae): their traits and systematic significance. ZooKeys 877: 133-159. https://doi.org/10.3897/zookeys.877.35715
Figure 25-34 Pupae; terminal sternites (25–27), setiform projection of pronotum (28), spine of pronotum (29), spine of abdomen (30, 31), functional spiracle (32). Cocoon (33, 34) 25Ontholestes murinus, female 26, 27Staphylinus erythropterus, female (26), male (27) 28Gabrius appendiculatus29Quedius cinctus30Quedionuchus plagiatus31Quedius cinctus32Atanygnathus terminalis, III pair 33Ontholestes murinus34Rabigus tenuis. Abbreviations: A accessory, S spine, Sap spiracular appendage, Tp terminal prolongation, Vp ventral prolongation.
Figure 14-24 from: Staniec B, Pietrykowska-Tudruj E (2019) Pupae of the mega-diverse rove beetle tribe Staphylinini (Coleoptera, Staphylinidae): their traits and systematic significance. ZooKeys 877: 133-159. https://doi.org/10.3897/zookeys.877.35715
Figure 14-24 Pupae; dorsal aspect (17), lateral aspect (15, 19, 23), ventral aspect (14, 16, 18, 20, 21, 22, 24), accessories of terminal prolongation (14a) 14, 14aGabrius appendiculatus15, 16Hesperus rufipennis17Bisnius fimetarius18, 19Atanygnathus terminalis20Heterothops praevius21Erichsonius cinerascens22Quedius fumatus23Q. cinctus24Q. microps.
Figure 1-13 from: Staniec B, Pietrykowska-Tudruj E (2019) Pupae of the mega-diverse rove beetle tribe Staphylinini (Coleoptera, Staphylinidae): their traits and systematic significance. ZooKeys 877: 133-159. https://doi.org/10.3897/zookeys.877.35715
Figure 1-13 Pupae; dorsal aspect (1, 3), ventral aspect (2, 4, 5, 6, 9, 10, 13), lower part in dorsal aspect (5a), lower part in ventral aspect (8a), upper part in dorsal aspect (11a, 12a), upper part in lateral aspect (5b, 6a, 11b, 12b), cuticular projection (2a, 6b, 13a), microstructure of the head (2b) 1–2bAcylophorus wagenschieberi3, 4Astrapaeus ulmi5–5bOntholestes murinus6–6bStaphylinus erythropterus7Creophilus maxillosus, tibiae I and II and antenna 8a, bOcypus fulvipennis9Tasgius melanarius10Neobisnius villosulus11a, bPhilonthus decorus12a, bP. succicola13, 13aRabigus tenuis. Abbreviations: An antenna, As atrophied spiracle, BL body length, BW body width, El elytra, Fs functional spiracle, Fti fore tibia, H head, HL head length, Hti hind tibia, HW head width, K knee, Li labium, Lr labrum, Md mandible, Mp maxillary palp, Ms mesonotum, Mt metanotum, Mti mid tibia, P pronotum, Pr protuberance, PW pronotum width, Sp setiform projection, St sternite, Tr tergite, W wing.
Fig. 2 in Cryptic and pseudo-cryptic diversity in the world's most common bark beetle-Hypothenemus eruditus
Fig. 2 Character states for Bbody color.^ a Bicolored (state 1). b Dark (state 2)
Fig. 1 A in Cryptic and pseudo-cryptic diversity in the world's most common bark beetle-Hypothenemus eruditus
Fig. 1 A piece of the book cover tunneled by beetles of the syntype series of Hypothenemus eruditus
Figure 6 in Deep soil floatation in Chile reveals diverse and mainly nameless fauna of endogean beetles (Coleoptera)
Figure 6. Maximum Likelihood DNA barcode tree of 85 non-Staphylinidae endogean beetles of Chile. Families are colour coded. Terminal names consist of specimen number, the family name (superfamily for specimens GR0312 and GR0313), the most detailed current taxonomic identification (species, genus, tribe, or subfamily), sample number, length of the DNA barcode fragment [with the number of ambiguously read bases in angle brackets], BIN number [if applicable, also denoted on the tree with black dots], and GenBank accession number. Digits at internodes are rapid bootstrap values of 50 % and above.
Figure 1 in Deep soil floatation in Chile reveals diverse and mainly nameless fauna of endogean beetles (Coleoptera)
Figure 1. (A) map of central Chile between Santiago and Valdivia showing the 15 localities where 50 deep soil samples were taken; (B) a pit producing the soil sample CH01 (note the piolet used for digging, a sifter used to sift the soil, and one bag of sifted soil ready to be floated in the barrel with water); (C) the floatation process, with the floating fraction scooped by a kitchen sieve and deposited on a fine mesh on the ground; (D) a standard floated sample after rinsing in water and before being wrapped in two additional layers of thicker cloth; (E) two plastic boxes used for sample transportation and temperature/humidity management, each containing 16 floated samples; (F) Sundriven specimen extraction with floated samples spread on chicken wire and placed on top of aluminium pans (note on the background a funnel suspended from a tree, through which water from all pans was filtered daily).
Figure 5 in Spatiotemporal patterns of ground beetle diversity (Coleoptera: Carabidae) in a Ramsar wetland (Chott Tinsilt) of Algeria
Figure 5. Hierarchical clustering dendrogram illustrating abundance-based similarity of ground beetle species among months in Chott Tinsilt, northeastern Algeria (clustering method = Euclidean paired group, UPGMA).
Fig. 3 in Rare or Simply Overlooked? New Records of Pediacus ater Grouvelle, 1897 from the Philippines, with Notes on Phenology and Diversity of its Flat Bark Beetle Fauna (Coleoptera: Cucujidae)
Fig. 3. Distribution of flat bark beetles (Cucujidae) in the Philippines.
Figure 4 from: Riley Peterson KN, Browne RA, Erwin TL (2021) Carabid beetle (Coleoptera, Carabidae) richness, diversity, and community structure in the understory of temporarily flooded and non-flooded Amazonian forests of Ecuador. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 831-876. https://doi.org/10.3897/zookeys.1044.62340
Figure 4 Body length (ABL) (mm) for carabid individuals collected in FP and TF forests, excluding Cicindelini. Body length for FP forest was significantly larger than TF forest (P < 0.001).
Figure E1 from: Riley Peterson KN, Browne RA, Erwin TL (2021) Carabid beetle (Coleoptera, Carabidae) richness, diversity, and community structure in the understory of temporarily flooded and non-flooded Amazonian forests of Ecuador. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 831-876. https://doi.org/10.3897/zookeys.1044.62340
Figure E1 Non-metric multidimensional scaling (NMDS) ordination based on Jaccard dissimilarity values (presence/absence data) of Carabidae morphospecies assemblages for FP and TF forests (stress = 13.7, k = 2). Each data point represents one of the 24 sampling sites. Significant differences (P < 0.001) in morphospecies assemblages occurred between FP and TF.
Figure D2 from: Riley Peterson KN, Browne RA, Erwin TL (2021) Carabid beetle (Coleoptera, Carabidae) richness, diversity, and community structure in the understory of temporarily flooded and non-flooded Amazonian forests of Ecuador. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 831-876. https://doi.org/10.3897/zookeys.1044.62340
Figure D2 Numbers of morphospecies for Carabidae tribes with significant differences (P < 0.05) between FP and TF forests.
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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
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.