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Fig. 8 in A revision of the Thyropygus allevatus group. Part V: Nine new species of the extended opinatus subgroup, based on morphological and DNA sequence data (Diplopoda: Spirostreptida: Harpagophoridae)
Fig. 8. Thyropygus sutchariti sp. nov., from Kaeng Krachan, holotype (CUMZ-D00090), ♂, gonopods. A. Anterior view, left telopodite removed. B. Posterior view, left telopodite removed. C. Left telopodite, posterior-mesal view. D. Left telopodite, anterior-lateral view.
Fig. 11. A in A revision of the Thyropygus allevatus group. Part V: Nine new species of the extended opinatus subgroup, based on morphological and DNA sequence data (Diplopoda: Spirostreptida: Harpagophoridae)
Fig. 11. A. Thyropygus navychula sp. nov., specimen from Surin Islands, living ♂ (paratype, CUMZ-D00089-1). B. Thyropygus forceps sp. nov., specimen from Namwang Srithammasokrach, living ♂ (paratype, CUMZ-D00073-1).
Fig. 5 in A revision of the Thyropygus allevatus group. Part V: Nine new species of the extended opinatus subgroup, based on morphological and DNA sequence data (Diplopoda: Spirostreptida: Harpagophoridae)
Fig. 5. Thyropygus mesocristatus sp. nov., from Srikasorn, holotype (CUMZ-D00094), ♂, gonopods. A. Anterior view, left telopodite removed. B. Posterior view, left telopodite removed. C. Lateral view. D. Left telopodite, posterior-mesal view. E. Left telopodite, anterior-lateral view.
Fig. 2 in A revision of the Thyropygus allevatus group. Part V: Nine new species of the extended opinatus subgroup, based on morphological and DNA sequence data (Diplopoda: Spirostreptida: Harpagophoridae)
Fig. 2. Thyropygus cimi sp. nov., from Namwang Srithammasokrach, holotype (CUMZ-D00086), ♂, gonopods. A. Anterior view, left telopodite removed. B. Posterior view, left telopodite removed. C. Lateral view. D. Left telopodite, posterior-mesal view. E. Left telopodite, anterior-lateral view.
Fig. 1 in A revision of the Thyropygus allevatus group. Part V: Nine new species of the extended opinatus subgroup, based on morphological and DNA sequence data (Diplopoda: Spirostreptida: Harpagophoridae)
Fig. 1. Phylogenetic relationships of Thyropygus species based on maximum likelihood analysis (ML) and Bayesian Inference (BI) of 1147 bp of concatenated gene fragments of COI (660 bp) and 16S rRNA (487 bp). Numbers at nodes indicate branch support based on bootstrapping (ML) / posterior probability (BI). Scale bar = 0.06 substitutions/site. # indicates branches which received <50% ML bootstrap support, - indicates non-supported branches by posterior probability. Clade memberships and designations are shown as vertical bars; 1A1 = T. allevatus, 1A2 = cuisinieri subgroup, 1A3 = opinatus subgroup and 1A4 = induratus subgroup. The coloured area marks the T. opinatus subgroup. Abbreviations after species names refer to locality names as shown in Table 1.
Fig. 7 in A revision of the Thyropygus allevatus group. Part V: Nine new species of the extended opinatus subgroup, based on morphological and DNA sequence data (Diplopoda: Spirostreptida: Harpagophoridae)
Fig. 7. Thyropygus planispina sp. nov., from Tham Sua temple, holotype (CUMZ-D00088), ♂, gonopods. A. Anterior view, left telopodite removed. B. Posterior view, left telopodite removed. C. Lateral view. D. Left telopodite, posterior-mesal view. E. Left telopodite, anterior-lateral view.
Fig. 6 in A revision of the Thyropygus allevatus group. Part V: Nine new species of the extended opinatus subgroup, based on morphological and DNA sequence data (Diplopoda: Spirostreptida: Harpagophoridae)
Fig. 6. Thyropygus navychula sp. nov., from Surin Islands, holotype (CUMZ-D00095), ♂, gonopods. A. Anterior view, left telopodite removed. B. Posterior view, left telopodite removed. C. Left telopodite, posterior-mesal view. D. Left telopodite, anterior-lateral view.
Fig. 4 in A revision of the Thyropygus allevatus group. Part V: Nine new species of the extended opinatus subgroup, based on morphological and DNA sequence data (Diplopoda: Spirostreptida: Harpagophoridae)
Fig. 4. Thyropygus forceps sp. nov., gonopods. – A, C–E. Holotype (CUMZ-D00092), ♂, from Namwang Srithammasokrach. A. Anterior view, left telopodite removed. C. Posterior view, left telopodite removed. D. Left telopodite, posterior-mesal view. E. Left telopodite, anterior-lateral view. – B. Specimen from Tham Pha Deang temple (CUMZ-D00093), ♂. Anterior view, left telopodite removed.
Fig. 10 in A revision of the Thyropygus allevatus group. Part V: Nine new species of the extended opinatus subgroup, based on morphological and DNA sequence data (Diplopoda: Spirostreptida: Harpagophoridae)
Fig. 10. Thyropygus ursus sp. nov., from Lanta Islands, holotype (NMHW-Inv.7855), ♂, gonopods. A. Anterior view, left telopodite removed. B. Posterior view, left telopodite removed. C. Left telopodite, posterior-mesal view. D. Left telopodite, anterior-lateral view.
Fig. 9 in A revision of the Thyropygus allevatus group. Part V: Nine new species of the extended opinatus subgroup, based on morphological and DNA sequence data (Diplopoda: Spirostreptida: Harpagophoridae)
Fig. 9. Thyropygus undulatus sp. nov., from Khao Phanom Bencha, holotype (CUMZ-D00087), ♂, gonopods. A. Anterior view, left telopodite removed. B. Posterior view, left telopodite removed. C. Lateral view. D. Left telopodite, posterior-mesal view. E. Left telopodite, anterior-lateral view.
Fig. 3 in A revision of the Thyropygus allevatus group. Part V: Nine new species of the extended opinatus subgroup, based on morphological and DNA sequence data (Diplopoda: Spirostreptida: Harpagophoridae)
Fig. 3. Thyropygus culter sp. nov., from Rorn waterfall, holotype (CUMZ-D00091), ♂, gonopods. A. Anterior view, left telopodite removed. B. Posterior view, left telopodite removed. C. Left telopodite, posterior-mesal view. D. Left telopodite, anterior-lateral view.
Neighbor-joining phylogenetic tree based on 16S rRNA sequences.
<p><strong>Supplementary Figure (S1):</strong> Bayesian 50% majority rule phylogram of 16S ribosomal RNA region showing the phylogenetic relationships among the bacterial isolates in our study. The newly generated sequences are preceded by red circle. The GenBank sequences are preceded by blue squares. The GenBank accession number appears after the species name. Numbers above the branches represent Bayesian posterior probabilities (≥ 0.90), and the maximum parsimony bootstrap support values are given below the branches (≥70%). The out group used for tree construction preceded by empty circle.</p>
CyclomicsSeq: Accurate detection of circulating tumor DNA using nanopore consensus sequencing
<p>CyclomicsSeq is a protocol designed to produce and sequence long DNA concatemers with a linear repetition to acquire high accuracy consensus reads. In this dataset, we used CyclomicsSeq for sequencing TP53 in cell-free DNA of healthy individuals and of head and neck cancer patients and for sequencing synthetic TP53 DNA sequences that mimic the length of cell-free DNA. This dataset contains data (mainly base calls of the backbone and the insert) of 32 nanopore sequencing runs. <br> </p>
Fig. 55. One ofthreetreesfromtotalevidenceanalysiswith POYof 92-taxondatasetusing 2 in Phylogenetic relationships of family groups in Pentatomoidea based on morphology and DNA sequences (Insecta: Heteroptera)
Fig. 55. One ofthreetreesfromtotalevidenceanalysiswith POYof 92-taxondatasetusing 2: 2 indel ⁄ transition–transversioncostratio, whichhad the lowest MRI value. Bremer support values are shown.
Fig. 53 in Phylogenetic relationships of family groups in Pentatomoidea based on morphology and DNA sequences (Insecta: Heteroptera)
Fig. 53. One of six trees from total evidence analysis with POY of 92-taxon data set using 1: 1 indel ⁄ transition–transversion cost ratio. (d) Non-homoplasious; (s) homoplasious.
Figs 45–48. 45. Oneoftwotreesderivedfromanalysisofcombinedmoleculardatawith 1 in Phylogenetic relationships of family groups in Pentatomoidea based on morphology and DNA sequences (Insecta: Heteroptera)
Figs 45–48. 45. Oneoftwotreesderivedfromanalysisofcombinedmoleculardatawith 1: 1 indel ⁄ transition–transversioncostratio. 46. Singletree derivedfromanalysisofcombinedmoleculardatawith 2: 2 indel ⁄ transition–transversioncostratio. 47. Singletreederivedfromanalysisof ~500 bp of 16S rRNAdatausing 1: 1 indel ⁄ transition–transversioncost ratio. 48. Singletreederivedfromanalysis of ~1800 bpof 18S rRNAusing 1: 1 indel ⁄ transition–transversioncostratio.
Fig. 43 in Phylogenetic relationships of family groups in Pentatomoidea based on morphology and DNA sequences (Insecta: Heteroptera)
Fig. 43. Strict consensus of three trees derived from successive weighting of the results shown in Fig. 42. (d) Non-homoplasious; (s) homoplasious.
Figs 16–24. 16 in Phylogenetic relationships of family groups in Pentatomoidea based on morphology and DNA sequences (Insecta: Heteroptera)
Figs 16–24. 16. Saileriola sandakanensis (Saileriolidae). Coxae of middle and hind legs more distant from each other. 17a. Cydnus aterrimus (Cydnidae): hind tibiae, posterior view; 17b. Dallasiellus dilatipes (Cydnidae): fore tibiae, anterior view. 18. Ruckesona vitrella (Saileriolidae). Abdominal trichobothria. 19. Serbana borneensis (Phloeidae). Abdominal trichobothria. 20. Atarsocoris sp. (Cydnidae). Abdominal trichobothria. 21. Edessa sp. (Pentatomidae). Abdominal spiracles well removed from lateral margins of sternum. 22. Phloea subquadrata (Phloeidae). Male abdominal segment VIII with spiracles. 23. Tessaratoma papillosa (Tessaratomidae). Spiracles on second segment totally exposed and far removed from lateral margins of sternum. 24. Ruckesona vitrella (Saileriolidae), female. Sternite VII split on the midline.
Fig. 5 in First insights into past biodiversity of giraffes based on mitochondrial sequences from museum specimens
Fig. 5. Giraffe subspecies of the Nile region. The map (extracted from Google Earth; https://www.google.com/intl/de/earth/) shows the geographical barriers (rivers and mountains) that may have isolated (at least temporarily) the subspecies Giraffa camelopardalis camelopardalis (Linnaeus, 1758) (red), G. c. antiquorum (Jardine, 1835) (yellow), G. c. rothschildi Lydekker, 1903 (green) and G. c. reticulata de Winton, 1899 (magenta). The question mark refers to the uncertain geographic origin of Zarafa (left) and the two specimens from Abyssinia (right) (see Discussion for more details).
Fig. 2 in First insights into past biodiversity of giraffes based on mitochondrial sequences from museum specimens
Fig. 2. Illustrations of historical giraffe specimens. A. The ʻGiraffe of Levaillantʼ, anonymous painting made in the late 18th century and early 19th century, exhibited in ʻhôtel de Magnyʼ, Jardin des Plantes in Paris (France). B. The ʻGiraffe from Sennaarʼ, representing a lithography of Zarafa (MNHN-1845-211) and the skull of a giraffe from the Cape region (Geoffroy Saint-Hilaire 1827). C. Drawing of the holotype of Giraffa camelopardalis congoensis Lydekker, 1903 (RMCA-452), housed in the Royal Museum of Central Africa, Tervuren (Belgium) (Lydekker 1904). D. Head drawings of the holotypes of G. c. cottoni Lydekker, 1904 (NHMUK-1904.1.21.1, left) and G. g. wardi Lydekker, 1904 (NHMUK-1903.11.18.1, right) (Lydekker 1914).
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.