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1,138 results for “cryptic diversity”
Fig. 4 in Cryptic and pseudo-cryptic diversity in the world's most common bark beetle-Hypothenemus eruditus
Fig. 4 Character states for Binterstrial declivital vestiture.^ a Sparse (state 1). b Medium (state 2). c Abundant (state 3)
Fig. 1 in Cryptic diversity, sympatry, and other integrative taxonomy scenarios in the Mexican Ceratozamia miqueliana complex (Zamiaceae)
Fig. 1 Distribution map of the species; inset: points 1 The Los Tuxtlas mountain range, 2 Uxpanapa-Chimalapas region, 3 Northern mountain range of Chiapas. The type localities for the species are represented by large figures
Fig. 6 Bachia trinitatis. a Crown view UWIMZ2010.12.44c. b Profile FMNH 49881. c Gular view. d Manus. e Pes. f. FMNH 49880d in The reduced limbed lizards of the genus Bachia (Reptilia, Squamata, Gymnophthalmidae); biogeography, cryptic diversity, and morphological convergence in the eastern Caribbean
Fig. 6 Bachia trinitatis. a Crown view UWIMZ2010.12.44c. b Profile FMNH 49881. c Gular view. d Manus. e Pes. f. FMNH 49880d cleared and stained manus; arrow points to the reduced first digit, not readily visible in complete specimens. Each bar is about 1 mm
Fig. 7 a, b in The reduced limbed lizards of the genus Bachia (Reptilia, Squamata, Gymnophthalmidae); biogeography, cryptic diversity, and morphological convergence in the eastern Caribbean
Fig. 7 a, b Bachia trinitatis from Flagstaff Hill, Tobago (JCM). c, d Bachia whitei sp. nov. UWIZM.2017.15.6. A female from Main Ridge Reserve, Tobago (JCM)
Fig. 2 in The reduced limbed lizards of the genus Bachia (Reptilia, Squamata, Gymnophthalmidae); biogeography, cryptic diversity, and morphological convergence in the eastern Caribbean
Fig. 2 Best ML trees for the concatenated mitochondrial and nuclear (12S + 16S rDNA + c-mos), mitochondrial (12S + 16S rDNA) and nuclear (c-mos) alignments. Asterisks (*) by nodes correspond to posterior probabilities (above nodes) recovered from the Bayesian
Fig. 5 in The reduced limbed lizards of the genus Bachia (Reptilia, Squamata, Gymnophthalmidae); biogeography, cryptic diversity, and morphological convergence in the eastern Caribbean
Fig. 5 Bachia alleni. KU315771 from Grenada. a Crown. b Profile. c Gular view. d Rear leg with four digits. Each bar is about 1 mm
Fig. 4 in The reduced limbed lizards of the genus Bachia (Reptilia, Squamata, Gymnophthalmidae); biogeography, cryptic diversity, and morphological convergence in the eastern Caribbean
Fig. 4 The discriminate function analysis (DA) on the left was done using 58 specimens of eastern Caribbean Bachia and 12 traits. Bachia alleni (1 dark blue). The blue outlier labeled alleni is the type specimen of B. a. parviceps. (3, 4) Bachia trinitatis is shown as two populations: Trinidad (orange), Tobago, and Little Tobago (green). (4) Bachia beebei sp. nov. (light blue). The DA on the right was done with 61 specimens of eastern Caribbean Bachia. Bachia alleni (dark blue). Bachia trinitatis is shown as two populations: Trinidad (orange), Tobago and Little
Fig. 8 in The reduced limbed lizards of the genus Bachia (Reptilia, Squamata, Gymnophthalmidae); biogeography, cryptic diversity, and morphological convergence in the eastern Caribbean
Fig. 8 Bachia beebei sp. nov. AMNH 137630. a Crown view note absence of prefrontals. b Profile. c Gular view. D. Manus, with three digits. e Pes with four digits. Each bar is about 1 mm
Fig. 2 in Biogeography, cryptic diversity, and queen dimorphism evolution of the Neotropical ant genus Ectatomma Smith, 1958 (Formicidae, Ectatomminae)
Fig. 2 Ultrametric tree of Ectatomma ants obtained from BEAST Bayesian relaxed molecular clock analysis of two mitochondrial genes and one nuclear gene. Ninety-five per cent highest posterior density divergence time estimates are presented as bars. Numbers on the scale at the foot of the figure represent millions of years. Corresponding geological epochs and their subdivisions are represented with differential
Fig. 3 in Biogeography, cryptic diversity, and queen dimorphism evolution of the Neotropical ant genus Ectatomma Smith, 1958 (Formicidae, Ectatomminae)
Fig. 3 Ancestral area reconstruction results from RASP Bayesian analyses of Ectatomma ants based on biogeographic regions of Morrone (2006). Pie chart colours correspond to the posterior probability frequencies for each node. Letters in parenthesis correspond
Fig. 1 in Biogeography, cryptic diversity, and queen dimorphism evolution of the Neotropical ant genus Ectatomma Smith, 1958 (Formicidae, Ectatomminae)
Fig. 1 Ectatomma ant species Bayesian phylogram obtained by Mr. Bayes analyses of two mitochondrial and one nuclear gene sequences. Node support is shown by two numbers, the first one corresponding to Bayesian posterior probabilities and the second one to bootstrap support
Fig. 7 in Cryptic diversity in the Mediterranean Temnothorax lichtensteini species complex (Hymenoptera:Formicidae)
Fig. 7 Dorsal view of Temnothorax laconicus sp.n. paratype worker (Profitis-Ilias-20110501-342 / CAS San Francisco / CASENT0906682)
Fig. 3 in Cryptic diversity in the Mediterranean Temnothorax lichtensteini species complex (Hymenoptera:Formicidae)
Fig. 3 Scatterplot of discriminant scores for T. laconicus sp.n. (red circles), T. lichtensteini "East Mediterranean cluster " (green diamonds), T. lichtensteini "West Mediterranean cluster " (blue rectangles) and T. lichtensteini type material (purple rectangle) is illustrated. Ellipses of 95 % range are given for each group
Fig. 6 in Cryptic diversity in the Mediterranean Temnothorax lichtensteini species complex (Hymenoptera:Formicidae)
Fig. 6 Lateral view of Temnothorax laconicus sp.n. paratype worker (Profitis-Ilias-20110501-342 / CAS San Francisco / CASENT0906682)
Fig. 2 in Cryptic diversity in the Mediterranean Temnothorax lichtensteini species complex (Hymenoptera:Formicidae)
Fig. 2 Dendrogram of NC-Ward clustering of three cryptic lineages T. lichtensteini with two subsets ("East Mediterranean cluster " and "West Mediterranean cluster ") and T. laconicus sp.n. ("Peloponnese cluster "). Sequence of information in the string designating the samples: abbreviation of geographic cluster hypothesis inferred from the three exploratory data analyses (EDA methods)—country— locality—date—sample number. Asterisk Position of the T. lichtensteini type series
Fig. 4 in Cryptic diversity in the Mediterranean Temnothorax lichtensteini species complex (Hymenoptera:Formicidae)
Fig. 4 Sampling sites of Temnothorax lichtensteini species-complex. Separate lineages are illustrated as follows: T. laconicus sp.n. (red circles), T. lichtensteini "East Mediterranean cluster " (green diamonds),
Fig. 2 in Molecules and morphology suggest cryptic species diversity and an overall complex taxonomy of fish scale geckos, genus Geckolepis
Fig. 2 Left: Simplified ND4 tree of Geckolepis showing major clades and lineages referred to as OTUs as shown in Fig. 1 (relationships of G. polylepis are derived from analyses of the 12S gene sequences). Major diagnostic morphological differences of each (or combined) OTU are summarized at the right of each respective clade (considers only adult
Fig. 2 in DNA barcode reveals high cryptic diversity in the commercially important Penaeini shrimps (Decapoda, Penaeidae)
Fig. 2 Occurrence of deposit errors registered on the Bold Systems platform for members of Penaeini. The X axis represents the BINs for which COI sequence deposit errors were verified. The Y axis repre-
Fig. 4 in DNA barcode reveals high cryptic diversity in the commercially important Penaeini shrimps (Decapoda, Penaeidae)
Fig. 4 Representation of the largest intraspecific genetic distances (MDR) calculated for each representative of the Penaeini tribe. The X axis presents the seven analyzed genera, while the Y axis represents the
Figure 4 in COI barcoding provides reliable species identification and pinpoints cryptic diversity in Western Palearctic amphibians
Figure 4. Representation of the barcoding gap for the Anura (upper panel) and Caudata (bottom panel) datasets. Each individual in the dataset is represented by a vertical line in: blue, when a barcoding gap exists (the bottom of the line representing the maximum intraspecific distance, and the top of the line representing the minimum interspecific distance);
ScienceDex guides
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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.