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2,620 results for “Molecular Phylogeny”
Fig. 9 in Revised classification and phylogeny of an Afrotropical species group based on molecular and morphological data, with the description of a new genus (Coleoptera: Scarabaeidae: Onthophagini)
Fig. 9 Vagina and receptaculum seminis of a Digitonthophagus bonasus, b D. gazella, c Phalops ardea, and d P. wittei. Scale bars = 0.5 mm
Fig. 8 in Revised classification and phylogeny of an Afrotropical species group based on molecular and morphological data, with the description of a new genus (Coleoptera: Scarabaeidae: Onthophagini)
Fig. 8 The endophallus sclerites of a Digitonthophagus bonasus, b D. gazella, c Phalops ardea, and d P. wittei. Scale bars = 0.5 mm
Fig. 2 in Revised classification and phylogeny of an Afrotropical species group based on molecular and morphological data, with the description of a new genus (Coleoptera: Scarabaeidae: Onthophagini)
Fig. 2 Points configuration for the geometric morphometrics analysis of the epipharynx, with the landmarks marked in black and the semilandmarks in dark gray. Scale bar = 0.5 mm
Fig. 8 in Tracking the variability of phenotypic traits on a molecular phylogeny: an example from scolopendrid centipedes in peninsular India
Fig. 8 Presence of a lateral spine on the coxopleuron (on one side) mapped onto phylogeny of Indian Digitipes
Fig. 3 in Tracking the variability of phenotypic traits on a molecular phylogeny: an example from scolopendrid centipedes in peninsular India
Fig. 3 Number of glabrous antennal articles mapped onto phylogeny of Indian Digitipes. Taxonomic identifications from Joshi and Edgecombe (2013). CES codes refer to specimen registration numbers
Fig. 1 in Topography and climatic fluctuations boosting speciation: biogeography and a molecular phylogeny of the East African genera Afroanthracites Hemp & Ingrisch and Afroagraecia Ingrisch & Hemp (Orthoptera, Tettigoniidae, Conocephalinae, Agraeciini)
Fig. 1 Map of East Africa in the area Tanzania and southern Kenya. Indicated are the volcanoes and mountain ranges harboring Afroanthracites species
Fig. 2 Bayesian 50 in Recovering the evolutionary history of Africa's most diverse viper genus: morphological and molecular phylogeny of Bitis (Reptilia: Squamata: Viperidae)
Fig. 2 Bayesian 50 % majority-rule consensus phylogram of Bitis species from partitioned analysis of four mitochondrial gene fragments (ND4, cyt b, 16S, and 12S; total of 1930 bp). Support values include
Fig. 2 in New insights into the systematics and molecular phylogeny of the Malagasy snake genus Liopholidophis suggest at least one rapid reversal of extreme sexual dimorphism in tail length
Fig. 2 Head drawings of Liopholidophis baderi sp. nov. (holotype, ZFMK 62235) in (a) dorsal and (b) lateral view
Fig. 2 ITS phylogeny and genetic distances from the 13 in DNA barcoding of brown Parmeliae (Parmeliaceae) species: a molecular approach for accurate specimen identification, emphasizing species in Greenland
Fig. 2 ITS phylogeny and genetic distances from the 13 brown Pakmeliae species occurring in Greenland. a Cartoon representation of the maximum likelihood ITS topology obtained from 372 brown Pakmeliae specimens. Values at each node indicate non-parametric bootstrap support; only support values>50% are shown (complete ITS topology is shown in Supplementary Figure, S1). b Box plots of ITS genetic distances estimated for each species and all interspecific distances. 'CO' =Cetkakiella commixta; 'AG' =Melaielia agiata; 'HE' = M. hepatizoi; 'ST' = M. stygia; 'EL' = Melaiohalea elegaitula; 'EX' = M. exaspekatula; 'IN' = M. iifumata; 'OL' =M. olivacea; 'SE' =M. septeitkioialis; 'DI' =Moitaielia disjuicta; 'PA' = M.
Fig. 6 in Phylogeny, molecular ecology and taxonomy of southern Iberian lineages of Triops mauritanicus (Crustacea: Notostraca)
Fig. 6 Resting-egg size in populations of Triops cancriformis and main lineages of T. mauritanicus (C = 'Cádiz' lineage; G = 'Gitanilla' lineage; MM = T. m. mauritanicus; MS = T. m. simplex; P = 'Portuguese' lineage; S. I = 'S.Iberian' lineage; T.c.c. = Triops c. cancriformis). Eggs from populations 082, 084, 058, 108–111, 119, 120–123, 130 and some eggs from population 103 obtained from lab cultures, remaining samples extracted from field-collected sediments; for details on populations see Table A1. Error bars indicate 95% confidence intervals
Fig. 5 in Phylogeny, molecular ecology and taxonomy of southern Iberian lineages of Triops mauritanicus (Crustacea: Notostraca)
Fig. 5 Unrooted NJ tree of squared Mahalanobis distances between group centroids obtained from discriminant function analysis of morphological data on adult males of all known Triops mauritanicus lineages. Abbreviations: T.m.m. = T. m. mauritanicus; T.m.s = T. m. simplex
Fig. A1 in Phylogeny, molecular ecology and taxonomy of southern Iberian lineages of Triops mauritanicus (Crustacea: Notostraca)
Fig. A1 ML tree based on COI sequences (RAxML program, setting 'estimate proportion of invariable sites'; best evolutionary model obtained by Modeltest was TrN+I+G, selected by AIC). ML bootstrap support (obtained with RAxML) given for selected branches. Outgroups [GenBank sequences of Lepidurus apus (accession number EF189669), L. arcticus (AF209067), L. couesii (DQ310622), L. lemmoni (GQ144447), Triops longicaudatus (DQ310623 and GQ144444), T. australiensis (DQ889135), T. granarius (GQ144446)] removed for clarity. Samples labelled, as applicable, with short names of main phylogenetic lineages (Table A1) followed by museum specimen tissue voucher numbers (MTD-TW; sequences submitted to GenBank, acc. nrs. FN691430–FN691444) or by GenBank accessions, or labelled with GenBank accessions containing numbers but no lineage data (samples with GenBank taxon labels apparently resulting from erroneous species identification, i.e. samples submitted to GenBank with invalid species names). Abbreviations: T.c. = Triops cancriformis; T.m. = T. mauritanicus
Fig. 3 in Nereididae (Annelida) phylogeny based on molecular data
Fig. 3 Maximum Likelihood tree showing previous and new proposed delineation for subfamilies within Nereididae. Values on nodes are bootstrap support. Color scheme identifies taxa placement in clades at subfamily level: 1, Fitzhugh (1987); 2, Santos et al. (2005); and 3, present study; *unnamed clades. Colored taxa are species for which mtDNA gene order is known and their respective classifications (as Park et al., 2016). Photos show species examples for each group: Namanereidinae, Namalycastis abiuma; Gymnonereidinae, Gymnonereis aff. crosslandi; Nereidinae, Alitta aff. succinea. Photos by Santos, C. and Alves, P.
Fig. 9 in High species diversity of fish tapeworms in congeneric hosts in Africa: revision of Monobothrioides (Cestoda: Caryophyllidea), including description of two new species and molecular phylogeny
Fig. 9 Distribution map of nominal Monobothrioides spp. according to existing voucher material. Ichthyological provinces are marked as follows: I. Maghreb, II. Nilo Sudan, IIa. Abyssinian subprovince, III. Upper Guinea, IV. Lower Guinea, V. Congo, VI. Quanza, VII. Zambezi, VIII. East Coast, IX. Southern province (map orig. M. Jirků; delimitation of ichthyological provinces modified after Lévêque et al. 2008)
Fig. 2 in High species diversity of fish tapeworms in congeneric hosts in Africa: revision of Monobothrioides (Cestoda: Caryophyllidea), including description of two new species and molecular phylogeny
Fig. 2 Monobothrioides cunningtoni Fuhrmann and Baer, 1925 from Parauchenoglanis punctatus, Central African Republic (a, c, d—IPCAS C-535/1) and Auchenoglanis occidentalis, Zambia (b—BMNH 1928.5.22.117–124; e—syntype; MHNG-PLAT-41609). a Complete specimen, dorsal view; b, c scolex; d terminal genitalia, ventral view; e cross section at the testicular level
Fig. 3 in High species diversity of fish tapeworms in congeneric hosts in Africa: revision of Monobothrioides (Cestoda: Caryophyllidea), including description of two new species and molecular phylogeny
Fig. 3 Monobothrioides chalmersius (Woodland, 1924) from Clarias spp. a complete worm from C. anguillaris, Senegal (MHNG-PLAT-34719), dorsal view; b anterior region with first testes situated very far posterior to anteriormost vitelline follicles; c scolex; d posterior region of syntype from C. anguillaris, Sudan (BMNH 1961.3.14.43), dorsal view
Fig. 1 in High species diversity of fish tapeworms in congeneric hosts in Africa: revision of Monobothrioides (Cestoda: Caryophyllidea), including description of two new species and molecular phylogeny
Fig. 1 Best-scoring maximum likelihood tree based on the concatenated (ssrDNA, lsrDNA) dataset estimated in IQ-TREE under the TIM2+F+R2 model. Nodal supports depict standard bootstrap values (1000 replicates); only values>50 are shown. The branch length scale bar indicates number of
FIGURE 3 in Molecular phylogeny and morphology reveal a new wood-inhabiting fungal species, Hyphoderma guangdongense (Polyporales, Basidiomycota), from China
FIGURE 3. Microscopic structures of Hyphoderma guangdongense (holotype, CLZhao 12657): basidiospores (A), basidia and basidioles (B), tubular cystidia (C), septate cystidia (D), a section of the hymenium (E). Bars: (A–C) = 5 µm; (D–E) = 10 µm.
FIGURE 3 in Molecular phylogeny and morphology reveal two new wood-inhabiting fungal species (Basidiomycota) from China
FIGURE 3. Microscopic structures of Candelabrochaete yunnanensis (holotype, CLZhao 26027): basidiospores (A), basidia and basidioles (B), cystidia (C), a section of the hymenium (D). Bars: A= 5 µm, (B–D) = 10 µm.
Figure 5 in Molecular phylogeny of Chinese raspy crickets (Orthoptera: Gryllacrididae) reveals incongruences in current classification
Figure 5. Abdominal terminal: male (A–F), female (G–I). A, Glolarnaca sp.; B, Neolarnaca sp.; C, Ha. bilobulata; D, Apt. quadrimaculata; E, Apt. biloba; F, T. huanglianensis sp. nov.. (Arrow in A indicates spines extending downwards from the base in the middle of each valve at the posterior margin of male abdominal tergite, arrow in F indicates styli.).
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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.