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3,878 results for “Molecular data”
Fig. 2 in Two new species of the genus Mystilus Distant (Hemiptera: Miridae: Mirinae) from Vietnam, with discussion on morphological variation based on molecular data, and a revised key for Mystilus species
Fig. 2. Dorsal and lateral habitus with variation of Mystilus frederici, new species. A, holotype, male; B, paratype, female; C, lateral view of male; D–F, variation of pronotum colouration. Scale bar = 1 mm.
Fig. 1 in Two new species of the genus Mystilus Distant (Hemiptera: Miridae: Mirinae) from Vietnam, with discussion on morphological variation based on molecular data, and a revised key for Mystilus species
Fig. 1. Dorsal and lateral habitus with variation of Mystilus carvalhoi, new species. A, holotype, male; B, paratype, female; C, lateral view of male; D–F, variation of pronotum colouration. Scale bar = 1 mm.
Fig. 3 in Two new species of the genus Mystilus Distant (Hemiptera: Miridae: Mirinae) from Vietnam, with discussion on morphological variation based on molecular data, and a revised key for Mystilus species
Fig. 3. Parameres and endosome of Mystilus spp. A–D, M. carvalhoi, new species; E–H, M. frederici, new species. A, E, left paramere; B, F, right paramere; C, D, G, H, endosoma; sc, sclerite; sg, secondary gonopore. Scale bar = 0.1 mm.
Figure 5 in Three ways to distinguish species: using behavioural, ecological, and molecular data to tell apart two closely related ants, Camponotus renggeri and Camponotus rufipes (Hymenoptera: Formicidae)
Figure 5. Box plots of Kimura two-parameter (K2P) distance of 672 bp cytochrome c oxidase subunit I sequences within and between Camponotus renggeri and Camponotus rufipes. Boxes indicate interquartile range (upper line, quartile 3; lower line, quartile 1). Horizontal lines with boxes indicate median and whiskers the minimum and the maximum values. Outliers are shown as individual circles.
Figure 4 in Three ways to distinguish species: using behavioural, ecological, and molecular data to tell apart two closely related ants, Camponotus renggeri and Camponotus rufipes (Hymenoptera: Formicidae)
Figure 4. Genetic structure analyses of Camponotus renggeri (yellow) and Camponotus rufipes (red) workers from Mogi- Guaçu (Brazil), using microsatellites. A, model-based assignment of individuals to the most likely number of clusters (K = 2) using STRUCTURE software. B, model-based assignment of individuals to different classes of hybrids or 'pure' species. Each individual is represented by a vertical line and the colours indicate the probability of the individual being assigned to a group in (A), or a hybrid or 'pure species' class in (B). C, scatterplot of the model-free principal coordinates analysis considering the two first principal coordinates (PCo1 and 2).
Figure 2 in Three ways to distinguish species: using behavioural, ecological, and molecular data to tell apart two closely related ants, Camponotus renggeri and Camponotus rufipes (Hymenoptera: Formicidae)
Figure 2. Main vegetation physiognomies of the cerrado reserve at Mogi-Guaçu, Brazil. Cerrado sensu stricto consists of a dense scrub of shrubs and trees and a fair amount of herbaceous vegetation, whereas the cerradão is a closed woodland with a reduced ground layer. Nests of Camponotus renggeri (N = 46) were found in cerrado sensu stricto (22%) and cerradão (78%), whereas Camponotus rufipes (N = 40) occurred only in cerrado sensu stricto. Drawing by L. Mota.
Figure 1 in Three ways to distinguish species: using behavioural, ecological, and molecular data to tell apart two closely related ants, Camponotus renggeri and Camponotus rufipes (Hymenoptera: Formicidae)
Figure 1. Workers of (A) Camponotus renggeri and (B) Camponotus rufipes. The two species are usually differentiated in the field by nuances in the integument colour (C. renggeri is shiny; C. rufipes is matte), and colour of the legs (yellowish in C. renggeri; reddish in C. rufipes). Photographs courtesy of L. Mota.
Figure 6 in Three ways to distinguish species: using behavioural, ecological, and molecular data to tell apart two closely related ants, Camponotus renggeri and Camponotus rufipes (Hymenoptera: Formicidae)
Figure 6. Analyses of the cytochrome c oxidase subunit I haplotypes of Camponotus renggeri (yellow) and Camponotus rufipes (red). A, neighbour-joining tree constructed with Kimura two-parameter distances between C. renggeri and C. rufipes with bootstrap support values based on 10 000 replications indicated on each branch. B, median-joining network amongst the obtained haplotypes. Values on the branches represent the numbers of mutational steps distinguishing the haplotypes, represented as circles whose areas are proportional to the number of individuals with that haplotype.
Figure 3 in Three ways to distinguish species: using behavioural, ecological, and molecular data to tell apart two closely related ants, Camponotus renggeri and Camponotus rufipes (Hymenoptera: Formicidae)
Figure 3. Frequency distribution of nest categories in Camponotus renggeri and Camponotus rufipes in the cerrado reserve at Mogi-Guaçu, Brazil. The species differed in the structure and building materials used for nesting.
Figure 6 in First record of Liposcelis entomophila (Enderlein) (Psocodea: Liposcelididae) from Sri Lanka based on morphological and molecular data
Figure 6. Neighbor-joining and maximum likelihood phylogenetic trees constructed based on COI. The number at each branch showed the percentage supported by bootstrap. A. Neighbor-joining tree. B. Maximum likelihood tree.
Figure 7 in First record of Liposcelis entomophila (Enderlein) (Psocodea: Liposcelididae) from Sri Lanka based on morphological and molecular data
Figure 7. Neighbor-joining and maximum likelihood phylogenetic trees constructed based on ITS2. The number at each branch showed the percentage supported by bootstrap. A. Neighbor-joining tree. B. Maximum likelihood tree.
Figures 2–4. Liposcelis entomophila, female. 2. Adult. 3 in First record of Liposcelis entomophila (Enderlein) (Psocodea: Liposcelididae) from Sri Lanka based on morphological and molecular data
Figures 2–4. Liposcelis entomophila, female. 2. Adult. 3. Pronotal setae (PNS, 3). 4. Prosternal setae (5). Scale bars: 2 = 1.0 mm; 3–4 = 0.1 mm.
Fig. 4 in New Bryodelphax species (Heterotardigrada: Echiniscidae) from Western Borneo (Sarawak), with new molecular data for the genus
Fig. 4. Close-up on various parts of dorsal armature of Bryodelphax arenosus sp. nov. A, faceting of sc and ornamented pattern of sl; B, ornamented pattern of pl; C, faceting of c. Abbreviations are the same as for Figure 1. Scale bars in μm.
Fig. 1 in New Bryodelphax species (Heterotardigrada: Echiniscidae) from Western Borneo (Sarawak), with new molecular data for the genus
Fig. 1. Map of the Malay Archipelago with the Wallace's line marked with red colour (signifies the western border of Wallacea). Asterisk = sampling locality (Bako Peninsula).
Fig. 6 in New Bryodelphax species (Heterotardigrada: Echiniscidae) from Western Borneo (Sarawak), with new molecular data for the genus
Fig. 6. The phylogenetic position of Bryodelphax Thulin, 1928 (red lineage) on the Bayesian Inference (BI) cladogram constructed from currently available 18S+28S rRNA sequences for Echiniscidae, with Echiniscoides sigismundi (M. Schultze, 1865) as the outgroup (see also Table 2). The Echiniscus evolutionary line is marked with blue colour. Values above branches indicate posterior probability values. Branches with support below 0.9 were collapsed.
Fig. 3 in New Bryodelphax species (Heterotardigrada: Echiniscidae) from Western Borneo (Sarawak), with new molecular data for the genus
Fig. 3. Bryodelphax arenosus sp. nov., habitus (PCM). A, dorsal view (paratype); B, dorsolateral view (paratype); C, holotype dorsal armature in close-up (claws III inserted in the upper right corner). Empty arrowheads indicate ornamented portions of dorsal plates, whereas white arrowhead points pedal plate IV devoid of dentate collar. Scale bars in μm.
Fig. 2 in New Bryodelphax species (Heterotardigrada: Echiniscidae) from Western Borneo (Sarawak), with new molecular data for the genus
Fig. 2. Schematic arrangement of plates on dorsum of Bryodelphax arenosus sp. nov. Abbreviations: c = the caudal plate; pl = lateral portion of the paired plate; sc = central portion of the scapular plate; sl = lateral portion of the scapular plate.
Fig. 5 in New Bryodelphax species (Heterotardigrada: Echiniscidae) from Western Borneo (Sarawak), with new molecular data for the genus
Fig. 5. Other Bryodelphax spp., habitus (PCM). A, B. asiaticus Kaczmarek & Michalczyk, 2004, dorsal view (paratype); B, B. parvulus Thulin, 1928, dorsal view (specimen from Öland, Sweden); C, B. parvulus, lateral view (specimen from Öland, Sweden). Scale bars in μm.
Molecular Determinants and Pharmacological Analysis for a Class of Competitive Non-transported Bicyclic Inhibitors of the Betaine/GABA Transporter BGT1: Modeling Data
<p>This archive contains the modeling data for the study <a href="https://www.frontiersin.org/articles/10.3389/fchem.2021.736457/full">"Molecular Determinants and Pharmacological Analysis for a Class of Competitive Non-transported Bicyclic Inhibitors of the Betaine/GABA Transporter BGT1"</a> (doi: 10.3389/fchem.2021.736457).</p> <p>The following data sets are available:</p> <ul> <li>Induced fit docking results of all mentioned compounds in the study: <br> ifd_hBGT1_occ_clustering_all_compounds.zip<br> </li> <li>MD simulations of bicyclo-GABA and compound 1 (100ns, 3 replica):<br> MD_simulation_bicyclo-GABA_run1.zip<br> MD_simulation_bicyclo-GABA_run2.zip<br> MD_simulation_bicyclo-GABA_run3.zip<br> MD_simulation_cmd1_run1.zip<br> MD_simulation_cmd1_run2.zip<br> MD_simulation_cmd1_run3.zip</li> </ul> <p>A detailed description of the methods is available in the aforementioned publication.</p> <p> </p> <p>The compound numbering in the uploaded files differs from the compound numbering in the mentioned study:</p> <p> </p> <p>study / upload</p> <p>bicyclo-GABA / cmd4</p> <p>1 / IIa</p> <p>2 /8-2</p> <p>3 / 8-3</p> <p>4a / 7-1</p> <p>4b / 7-2</p> <p>4c / 7-3</p> <p> </p> <p> </p> <p> </p> <p> </p> <p> </p> <p> </p>
Fig. 6 in Three new species of Ligophorus Euzet & Suriano, 1977 (Monogenea: Ancyrocephalidae) from Moolgarda buchanani (Bleeker) off Johor, Malaysia based on morphological, morphometric and molecular data
Fig. 6. Sclerotised hard parts of L. grandis, new species: A, dorsal anchors; B, dorsal bar; C, ventral anchors; D, ventral bar (dorsal view); E, marginal hook; F, male copulatory organ.
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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.