Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
13,017
datasets available to search
ShareScore release 0.9.0
Dataset results
13,017 results for “Positionning”
Figure 1 from: Conrado AC, Arruda H, Stanton DWG, James SW, Kille P, Brown G, Silva E, Dupont L, Taheri S, Morgan AJ, Simões N, Rodrigues A, Montiel R, Cunha L (2017) The complete mitochondrial DNA sequence of the pantropical earthworm Pontoscolex corethrurus (Rhinodrilidae, Clitellata): Mitogenome characterization and phylogenetic positioning. ZooKeys 688: 1-13. https://doi.org/10.3897/zookeys.688.13721
Figure 1 - The mitochondrial genome of Pontoscolex corethrurus (Müller, 1857). Gene order and positions are shown, including the putative control region. IUPAC single letter codes are used to identify transfer RNA. The L1, L2, S1, and S2 transfer RNAs are differentiated on the basis of their anti-codons TAG, TAA, TCT, and TGA, respectively.
Figure 2 from: Conrado AC, Arruda H, Stanton DWG, James SW, Kille P, Brown G, Silva E, Dupont L, Taheri S, Morgan AJ, Simões N, Rodrigues A, Montiel R, Cunha L (2017) The complete mitochondrial DNA sequence of the pantropical earthworm Pontoscolex corethrurus (Rhinodrilidae, Clitellata): Mitogenome characterization and phylogenetic positioning. ZooKeys 688: 1-13. https://doi.org/10.3897/zookeys.688.13721
Figure 2 - Phylogenetic relationships among phylum Annelida based on the combined 13,416 bp nucleotide positions. Total alignment length is greater than the combined P. corethrurus protein coding and rRNA sequence lengths due to overlapping protein coding sequences that are subsequently concatenated, and indel regions in the alignment. The posterior probability value of BI analyses and bootstrap support values of ML analyses (in the order: BI, ML) are indicated near the branches.
Figure 3 from: Takano A (2017) Taxonomic study on Japanese Salvia (Lamiaceae): Phylogenetic position of S. akiensis, and polyphyletic nature of S. lutescens var. intermedia. PhytoKeys 80: 87-104. https://doi.org/10.3897/phytokeys.80.11611
Figure 3 - A graph shows the number of specimens examined indumentums at the base of anther connective.
Figure 2 from: Takano A (2017) Taxonomic study on Japanese Salvia (Lamiaceae): Phylogenetic position of S. akiensis, and polyphyletic nature of S. lutescens var. intermedia. PhytoKeys 80: 87-104. https://doi.org/10.3897/phytokeys.80.11611
Figure 2 - Photographs of S. lutescens var. intermedia flowers. a Flower of A. Takano 140806-4-2 (Hyogo), from Mt. Mikuni, Susono-shi, Shizuoka Pref. (Kanto region). Arrows indicate the base of the anther connective. No hairs are visible b Flower of A. Takano 140813-1 (Hyogo), from Mt. Yamatokatsuragi, Gose-shi, Nara Pref. (Kinki region). The red open circle indicates the base of the anther connective. White hairs are visible.
Figure 5 from: Takano A (2017) Taxonomic study on Japanese Salvia (Lamiaceae): Phylogenetic position of S. akiensis, and polyphyletic nature of S. lutescens var. intermedia. PhytoKeys 80: 87-104. https://doi.org/10.3897/phytokeys.80.11611
Figure 5 - The Bayesian maximum clade credibility tree derived from nuclear ribosomal DNA (concatenate dataset of ETS and ITS). ML-bootstrap/Bayesian-PP numbers are shown above or below the corresponding branch. Thick lines denote a clade that was strongly supported with ML-bootstrap and/or Bayesian-PP values greater than 95 %. ML: maximum likelihood; PP: posterior probability.
Figure 4 from: Takano A (2017) Taxonomic study on Japanese Salvia (Lamiaceae): Phylogenetic position of S. akiensis, and polyphyletic nature of S. lutescens var. intermedia. PhytoKeys 80: 87-104. https://doi.org/10.3897/phytokeys.80.11611
Figure 4 - The Bayesian maximum clade credibility tree derived from plastid DNA (concatenate dataset of rbcL, trnL-F, ycf1-rps15). ML-bootstrap/Bayesian PP numbers are shown near the corresponding branch. Thick lines denote a clade that was strongly supported, with ML- bootstrap and/or Bayesian-PP greater than 95 %. ML: maximum likelihood; PP: posterior probability.
Figure 1 from: Takano A (2017) Taxonomic study on Japanese Salvia (Lamiaceae): Phylogenetic position of S. akiensis, and polyphyletic nature of S. lutescens var. intermedia. PhytoKeys 80: 87-104. https://doi.org/10.3897/phytokeys.80.11611
Figure 1 - Map of Japan shows the sites where Salvia lutescens taxa were sampled. Open circle = var. crenata, filled circle = var. intermedia, open square = var. lutescens, filled square = var. stolonifera. The areas encircled with dotted lines show the Kinki and Kanto regions, as indicated.
Figure 3 from: Özüdoğru B, Fırat (2016) Arabis watsonii (P.H.Davis) F.K.Mey.: An overlooked cruciferous species from eastern Anatolia and its phylogenetic position. PhytoKeys 75: 57-68. https://doi.org/10.3897/phytokeys.75.10568
Figure 3 - ITS-based phylogenetic backbone of Arabideae that focuses on the placement of Arabis watsonii. Shown is the Bayesian maximum clade credibility tree with posterior probability values > 0.5. Highlighted part of the tree, (magnified on the left), is the Arabis hirsuta aggregate and its relatives. Color codes: Green = Arabis hirsuta aggregate, red=the closest relatives of the Arabis hirsuta aggregate, blue = Arabis watsonii. Clade names follow Karl and Koch (2013).
Figure 1 from: Özüdoğru B, Fırat (2016) Arabis watsonii (P.H.Davis) F.K.Mey.: An overlooked cruciferous species from eastern Anatolia and its phylogenetic position. PhytoKeys 75: 57-68. https://doi.org/10.3897/phytokeys.75.10568
Figure 1 - Photographs of Arabis watsonii, A habit (in flower) B habit (in fruit), C basal leaves D stem leaves E trichomes on leaves margins F flowers G fruits E habitat of Bahçesaray population.
Figure 4 from: Özüdoğru B, Fırat (2016) Arabis watsonii (P.H.Davis) F.K.Mey.: An overlooked cruciferous species from eastern Anatolia and its phylogenetic position. PhytoKeys 75: 57-68. https://doi.org/10.3897/phytokeys.75.10568
Figure 4 - trnL-F-based phylogenetic backbone of Arabideae that focuses on the placement of Arabis watsonii. Shown is the Bayesian maximum clade credibility tree with posterior probability values > 0.5. Highlighted part of the tree, (magnified on the left), is the Arabis hirsuta aggregate and its relatives. Color codes: Green = Arabis hirsuta aggregate, red=the closest relatives of the Arabis hirsuta aggregate, blue = Arabis watsonii. Clade names follow Karl and Koch (2013).
Figures 12-19 from: Skuhravá M, Massa B, Cerasa G (2016) Rediscovery and identity of Pumilomyia protrahenda De Stefani (Diptera, Cecidomyiidae) in Sicily with redescription and reassessment of its taxonomic position. ZooKeys 617: 129-137. https://doi.org/10.3897/zookeys.617.9850
Figures 12-19 - Rhopalomyia protrahenda comb. n. 12 Female, wing 13 male, first flagellomeres 14 female, fifth tarsomeres 15 female, antenna 16 female, first flagellomeres 17 female, claws and empodium 18 male terminalia, lateral view 19 frontal view.
Figures 20-29 from: Skuhravá M, Massa B, Cerasa G (2016) Rediscovery and identity of Pumilomyia protrahenda De Stefani (Diptera, Cecidomyiidae) in Sicily with redescription and reassessment of its taxonomic position. ZooKeys 617: 129-137. https://doi.org/10.3897/zookeys.617.9850
Figures 20-29 - 20 Artemisia arborescens covered with galls 21 female of Rhopalomyia protrahenda next to apical leaves of the host plant covered with reddish mass of eggs 22 galls, detail 23 dissected gall showing a pupa 24 exuviae protruding from a gall 25 adult emergence hole 26 detail of a leaf gall showing the chamber and thin wall 27 pupa, lateral view 28 pupa frontal view 29 female emerging from gall.
Figures 1-11 from: Skuhravá M, Massa B, Cerasa G (2016) Rediscovery and identity of Pumilomyia protrahenda De Stefani (Diptera, Cecidomyiidae) in Sicily with redescription and reassessment of its taxonomic position. ZooKeys 617: 129-137. https://doi.org/10.3897/zookeys.617.9850
Figures 1-11 - Rhopalomyia protrahenda comb. n. 1 Females wing 2 female, fifth flagellomere 3 female, two apical flagellomeres 4 female, head 5 male, fifth flagellomere 6 male, two apical flagellomeres 7 female, mouthparts 8 fifth tarsomere with simple claw and empodium 9 terminal part of ovipositor 10 pupal head, lateral view 11 male terminalia.
FIGURES 24–25 in Resurgence of a forgotten Southern Brazil endemic species: taxonomic position, redescription, and spatio-temporal distribution of Porosagrotis carolia Schaus, 1929 (Lepidoptera: Noctuidae: Noctuinae)
FIGURES 24–25. Feltia carolia (Schaus, 1929) comb. nov., male wing shape and venation.
Figure 2 from: Zhu Z-X, Xu H-X, Zhuang W-Y, Li Y (2017) Two new green-spored species of Trichoderma (Sordariomycetes, Ascomycota) and their phylogenetic positions. MycoKeys 26: 61-75. https://doi.org/10.3897/mycokeys.26.14919
Figure 2 - The new species Trichoderma fujianense, holotype (HMJAU 34830). a–s Asexual state a–c Cultures after 13 d at 25 °C (a PDA, b CMD, c SNA). d–q Conidiophores and phialides (SNA, 20 d) r, s Conidia (SNA, 20 d). Scales bars: 20 mm (a–c); 20 μm (d–h); 10 μm (i–s).
Figure 1 from: Zhu Z-X, Xu H-X, Zhuang W-Y, Li Y (2017) Two new green-spored species of Trichoderma (Sordariomycetes, Ascomycota) and their phylogenetic positions. MycoKeys 26: 61-75. https://doi.org/10.3897/mycokeys.26.14919
Figure 1 - Maximum parsimony phylogram reconstructed from the combined squences of RPB2 and TEF1-α. MPBP above 50% (left) and BIPP above 90% (right) are indicated at the nodes.
Figure 3 from: Zhu Z-X, Xu H-X, Zhuang W-Y, Li Y (2017) Two new green-spored species of Trichoderma (Sordariomycetes, Ascomycota) and their phylogenetic positions. MycoKeys 26: 61-75. https://doi.org/10.3897/mycokeys.26.14919
Figure 3 - The new species Trichoderma zonatum, holotype (HMJAU 34820). a–o Sexual state. a–g Dry stromata on nature substrate h Mature stroma after rehydration i Perithecium in section j Cortical and subcortical tissue in section k Subperithecial tissue in section l Stroma base in section. m–o Ascus with part-ascospores. p–aa Asexual state. p–r Cultures after 7 d at 25 °C (p PDA, q CMD, r SNA). s–y Conidiophores and phialides (SNA, 7 d). z, aa Conidia (SNA, 7 d). Scales bars: 2 mm (a); 1 mm (b, g); 500 μm (c–f, h); 20 μm (i–l, s, x, y); 5 μm (m–o, z, aa); 20 mm (p–r); 10 μm (t–w).
Figure 1 from: Krinitsina AA, Belenikin MS, Churikova OA, Kuptsov SV, Antipin MI, Logacheva MD, Speranskaya AS (2017) Systematic position of Dryopteris blanfordii subsp. nigrosquamosa (Ching) Fraser-Jenkins within the genus Dryopteris Adans.. PhytoKeys 90: 89-112. https://doi.org/10.3897/phytokeys.88.14745
Figure 1 - Dryopteris blanfordii subsp. nigrosquamosa morphology. A Frond of mature plants B Petiole covered with scales C Petiole scale D Adaxial surface of rachis and costa E Abaxial surface of rachis and costa.
Figure 2 from: Krinitsina AA, Belenikin MS, Churikova OA, Kuptsov SV, Antipin MI, Logacheva MD, Speranskaya AS (2017) Systematic position of Dryopteris blanfordii subsp. nigrosquamosa (Ching) Fraser-Jenkins within the genus Dryopteris Adans.. PhytoKeys 90: 89-112. https://doi.org/10.3897/phytokeys.88.14745
Figure 2 - Topology from ML and BI analyses of Dryopteris species using six marker regions consisting of 3734 total bases (psbA-trnH, rbcL-accD, rbcL, trnL-trnF, trnP-petG, rps4-trnS and matK). The tree is drawn to scale, with branch lengths measured in the number of substitutions per site. Bootstrap values are specified at the branch nodes (cut off >50%) / Bayesian РР. Dryopteris blanfordii subsp. nigrosquamosa and closely related species are marked with a blue rectangle.
Figure 8 from: Ezzine IK, Pfarrer B, Dimassi N, Said K, Neubert E (2017) At home at least: the taxonomic position of some north African Xerocrassa species (Pulmonata, Geomitridae). ZooKeys 712: 1-27. https://doi.org/10.3897/zookeys.712.13066
Figure 8 - Haplotype Network showed the number of variable sites. A Haplotypes and numbers of variables sites based on mitochondrial markers B Haplotypes numbers of variables sites based on concatenated mitochondrial and nuclear data.
ScienceDex guides
Understand access before you commit
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.