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.
284
datasets available to search
ShareScore release 0.9.0
Dataset results
284 results for “novel genus”
Figure 8 in Morphological, ontogenetic, and molecular investigations of freshwater hypotrich ciliates from China revealed a new genus Heterodeviata gen. nov. (Protista: Ciliophora), and a novel limnetic population of Deviata multilineae
Figure 8. Nucleotide differences between deviatids based on 18S rRNA gene sequences. In (A), the lower less values of the table indicate the sequence similarity, the upper right numbers are numbers of nucleotide differences. The numbers in the header (B) indicate the unmatched site positions. In A, B, the newly obtained sequences are in red. '**' indicates the sequence Perisincirra sp. (KY855575) which was likely misidentified and can be considered conspecific with Deviata brasiliensis. 'H', Heterodeviata.
Figure 5 in Morphological, ontogenetic, and molecular investigations of freshwater hypotrich ciliates from China revealed a new genus Heterodeviata gen. nov. (Protista: Ciliophora), and a novel limnetic population of Deviata multilineae
Figure 5. Morphogenetic process of Heterodeviata sinica asser protargol impregnation. A, showing the oral primordium of the opisthe. B, ventral view of a very early divider, showing oral primordium of the opisthe (arrowhead). C–E, ventro-lateral (C, D) and dorsolateral (E) views of the same early divider, in this stage, anlagen I–IV (C), two right marginal anlagen (E) formed, adoral zone of membranelles incompletely formed (arrowhead in C), and arrowhead in (D) shows the parental endoral beginning to disintegrate. F, G, ventral (F) and dorsal (G) views of two middle dividers, arrowheads in (G) showing dorsal kinety anlage 2. H, I, ventral (H) and dorsal view (I) of two middle dividers, in this stage, anlagen I–IV dedifferentiating into cirri (H), and two bristles of dorsal kinety 2 formed (arrowheads in H, I). J, dorsal view of a late divider, showing one macronuclear nodule dedifferentiated into two ones. K, L, ventral views of two late dividers, arrowheads in (K) and (L) indicate the buccal and parabuccal cirrus, separately. I–IV, anlagen I–IV; DK1, dorsal kinety 1; DḎ1, dorsal kinety anlage 1; FVR, frontoventral cirral row; LMA1, 2, less marginal anlagen 1, 2; LMR1, 2, less marginal rows 1, 2; Ma, macronuclear nodules; Mi, micronuclei; OP, oral primordium; RMA1, 2, right marginal anlagen 1, 2; RMR1, 2, right marginal rows 1, 2; UM, undulating membranes. Scale bars: 50 μm (F, L), 20 μm (G, I).
Figure 1 in Morphological, ontogenetic, and molecular investigations of freshwater hypotrich ciliates from China revealed a new genus Heterodeviata gen. nov. (Protista: Ciliophora), and a novel limnetic population of Deviata multilineae
Figure 1. Location of the sampling site. A, map showing the location of the Lake Weishan Wetland, China. B, C, photographs of the Lake Weishan where Heterodeviata sinica and Deviata multilineae were collected, respectively.
Figure 9 in Morphological, ontogenetic, and molecular investigations of freshwater hypotrich ciliates from China revealed a new genus Heterodeviata gen. nov. (Protista: Ciliophora), and a novel limnetic population of Deviata multilineae
Figure 9. Comparison of Heterodeviata with related genera within Deviatidae and Kahllidae that possess three frontal cirri, at least one short or long frontal ventral cirral row right of the cell midline, at least one less marginal row, and one dorsomarginal kinety. Figures in the upper and lower row show the dorsal kinety paưern and cirral paưern of corresponding genera, respectively. Old (parental) structures (marginal cirri or dorsal kineties) are depicted by contour. Abbreviations: BC, buccal cirri; CC, caudal cirri; DK, dorsal kinety; FC, frontal cirri; FVR, frontoventral cirral row; LMR, less marginal row; PBC, parabuccal cirri; RMR, right marginal row; TC, transverse cirri.
Figure 4 in Morphological, ontogenetic, and molecular investigations of freshwater hypotrich ciliates from China revealed a new genus Heterodeviata gen. nov. (Protista: Ciliophora), and a novel limnetic population of Deviata multilineae
Figure 4. Early to middle morphogenetic stages of Heterodeviata sinica asser protargol impregnation. A, macronuclear nodules of a very early divider (ventral view), showing replication band of macronuclear nodules (arrows). B, oral primordium of the opisthe (arrow). C, developed oral primordia (arrow). D–F, ventrolateral (D, E) and dorsolateral (F) view of the same early divider, showing incomplete adoral zone of membranelles (arrow in D, E), the intrakinetally formed marginal anlagen and dorsal kinety anlage 1. G, H, ventral (G) and dorsal (H) view of the same early-middle divider, showing the dorsal kinety 2 anlage formed to the right of the right marginal anlage 2. I, J, ventral (I) and dorsal (J) view of the same middle divider, denoting anlagen I–IV differentiating into cirri, arrowhead in (I) shows the parabuccal cirrus. DḎ1, 2, dorsal kineties anlagen 1, 2; FC, frontal cirri; FVR, frontoventral cirral row; LMA1, 2, less marginal anlagen 1, 2; Ma, macronuclear nodules; Mi, micronuclei; RMA1, 2, right marginal anlagen 1, 2; UMA, undulating membrane anlage. Scale bars: 20 μm (A–C), 50 μm (D–J).
Figure 3 in Morphological, ontogenetic, and molecular investigations of freshwater hypotrich ciliates from China revealed a new genus Heterodeviata gen. nov. (Protista: Ciliophora), and a novel limnetic population of Deviata multilineae
Figure 3. Heterodeviata sinica from life (A, D–F, I–K) and asser protargol impregnation (B, C, G, H, L–P). A, ventral view of a composite representative specimen. B, L, details of the oral zone, arrow in (B) indicates pharyngeal fibres. C, detail of the end of cell, arrowhead indicates the caudal cirrus at the end of dorsal kinety 1. D–F, ventral views, showing the various cell shapes, arrows mark the contractile vacuole. G, H, M–O, ventral (G, N) and dorsal (H, M, O) views of the holotype, denoting infraciliature and nuclear apparatus, arrowhead in (G) marks buccal cirrus, arrowheads in (H, O) and arrow in (M, O) show the two dorsal bristles of dorsal kinety 2 and the single caudal cirrus, respectively. I, J, ventral views to show different individuals, arrow in (I) shows contractile vacuole. K, showing the cytoplasm and macronuclear nodules. P, dorsal view of a different individual, arrowheads and arrow indicate two dorsal bristles and caudal cirrus, respectively. 1, 2, dorsal kineties 1, 2; E, endoral; FC, frontal cirri; FVR, frontoventral cirral row; LMR1, 2, less marginal rows 1, 2; Ma, macronuclear nodules; Mi, micronuclei; P, paroral; PBC, parabuccal cirri; RMR1, 2, right marginal rows 1, 2. Scale bars: 50 μm (A, D–F, I, J), 30 μm (G, H, K–P).
Figure 6 in Morphological, ontogenetic, and molecular investigations of freshwater hypotrich ciliates from China revealed a new genus Heterodeviata gen. nov. (Protista: Ciliophora), and a novel limnetic population of Deviata multilineae
Figure 6. Middle to late morphogenetic stages of Heterodeviata sinica asser protargol impregnation. A, B, ventral (A) and dorsal (B) view of the same middle divider, to demonstrate the formed marginal rows and dorsal kineties 1, 2. C, D, ventral (C) and dorsal (D) view of the same late-middle divider, arrowheads in (C) show the parabuccal cirrus. E, F, ventral (E) and dorsal (F) view of the same late divider, arrowheads in (E) and arrows in (F) separately mark the parabuccal and caudal cirrus for the proter and opisthe. G, H, ventral (G) and dorsal (H) view of the same late divider, arrowheads and arrows separately show the parabuccal and caudal cirrus. BC, buccal cirrus, DK1, 2, dorsal kineties 1, 2; FC, frontal cirri; FVR, frontoventral cirral row; LMR1, 2, less marginal rows 1, 2; Ma, macronuclear nodules; RMR1, 2, right marginal rows 1, 2. Scale bars: 50 μm.
Figure 2. A, maximum likelihood tree inferred from 18S in Morphological, ontogenetic, and molecular investigations of freshwater hypotrich ciliates from China revealed a new genus Heterodeviata gen. nov. (Protista: Ciliophora), and a novel limnetic population of Deviata multilineae
Figure 2. A, maximum likelihood tree inferred from 18S rRNA gene sequences, showing the phylogenetic positions of the two newly sequenced species. Numbers near the nodes represent the ML bootstrap support and BI posterior probability values. Fully supported (100%/1.00) branches are marked with solid circles. 'Asterisks' indicate disagreement between the ML and BI trees. Sequences newly obtained are in pink. The scale bar corresponds to one substitution per 100 nucleotide positions. B, the tree is made referring to the ML tree in a radiation view, showing the likely systematic relationship of Heterodeviata with related genera. C, topology of species within Deviatidae in Bayesian inference (BI) tree. '**' indicates the sequence Perisincirra sp. (KY855575) is probably misidentified, which should be conspecific with Deviata brasiliensis.
Data from: Independent evolution of ancestral and novel defenses in a genus of toxic plants (Erysimum, Brassicaceae)
Open the record for dataset details and reuse information.
Fig. 6 in A novel species of Heterophoxus Shoemaker, 1925 (Crustacea, Amphipoda, Phoxocephalidae) from southeast and southern Brazil, with an identification key to world species of the genus
Fig. 6. Heterophoxus shoemakeri sp. nov. A–F. Paratype, ♂ (UERJ 434). A. Head. B. Antenna 1. C. Antenna 2. D. Gnathopod 1. E. Gnathopod 2. F. Uropod 3. G. Paratype, subadult ♂ (UERJ 435). Antenna 2. Scale bars: A = 0.5 mm; B–F = 0.2 mm; G = 0.1 mm.
Fig. 5 in A novel species of Heterophoxus Shoemaker, 1925 (Crustacea, Amphipoda, Phoxocephalidae) from southeast and southern Brazil, with an identification key to world species of the genus
Fig. 5. Heterophoxus shoemakeri sp. nov., holotype, ♀ (UERJ 433). A. Epimeral plate 1. B. Epimeral plate 2. C. Epimeral plate 3. D. Uropod 1 E. Uropod 2. F. Uropod 3. G. Telson. Scale bars: A–E, G = 0.2 mm; F = 0.1 mm.
Fig. 4 in A novel species of Heterophoxus Shoemaker, 1925 (Crustacea, Amphipoda, Phoxocephalidae) from southeast and southern Brazil, with an identification key to world species of the genus
Fig. 4. Heterophoxus shoemakeri sp. nov., holotype, ♀ (UERJ 433). A. Pereopod 5. B. Pereopod 6. C. Pereopod 7. Scale bars = 0.2 mm.
Figure 2 from: Zheng H, Wan Y, Li J, Castañeda-Ruiz RF, Yu Z (2020) Phialolunulospora vermispora (Chaetosphaeriaceae, Sordariomycetes), a novel asexual genus and species from freshwater in southern China. MycoKeys 76: 17-30. https://doi.org/10.3897/mycokeys.76.57410
Figure 2 Phialolunulospora vermispora (YMF 1.04260) A colony on PDA at day 10 B conidia C–F conidiophores, conidiogenous cells and conidia G conidiogenous cells H, I conidiophores and conidiogenous cells. Scale bars: 10 mm (A); 10 μm (B–I).
Figure 1 from: Zheng H, Wan Y, Li J, Castañeda-Ruiz RF, Yu Z (2020) Phialolunulospora vermispora (Chaetosphaeriaceae, Sordariomycetes), a novel asexual genus and species from freshwater in southern China. MycoKeys 76: 17-30. https://doi.org/10.3897/mycokeys.76.57410
Figure 1 Phylogenetic tree derived from Bayesian analysis based on ITS and LSU sequences, depicting the relationships of the new taxon Phialolunulospora vermispora with closely related taxa. The numbers above branches represent BIPP (left) and MLBPs (right). BIPP over 95% and MLBPs greater than 70% are shown on the respective branches, and the bar represents the substitutions per nucleotide position. Gelasinospora tetrasperma CBS 178.33, Sordaria fimicola CBS 508.50 and Lasiosphaeria ovina SMH 4605 were used as outgroup.
Fig. 11 in A new tarantula (Mygalomorphae: Theraphosidae) genus endemic from Peru with a novel genitalic morphology among theraphosinae and its phylogenetic placement
Fig. 11. Distribution map of Chinchaysuyu gen. nov. in Peru.
Figure 1 from: Yuhui X, Lijun Z, Yue H, Xiaoqi W, Chen Z, Huilun Z, Ruoran W, Da P, Hongying S (2017) Complete mitochondrial genomes from two species of Chinese freshwater crabs of the genus Sinopotamon recovered using next-generation sequencing reveal a novel gene order (Brachyura, Potamidae). ZooKeys 705: 41-60. https://doi.org/10.3897/zookeys.705.11852
Figure 1 - Mitochondrial genome sequenced in the present study. Gene order and sizes are shown relative to one another, including non-coding regions. Protein-coding genes encoded on the light strand are underlined. Transfer RNA (tRNA) genes encoded on the light strand are underlined. Each tRNA gene is designated by a single-letter amino acid code, except L1 (trnLeu (CUN)), L2 (trnLeu (UUR)), S1 (trnSer (AGN)) and S2 (trnSer (UCN)). Numbers inside circles represent the size of the non-coding region separating two adjacent genes or the amount of shared nucleotides between two overlapping genes. The translocations of gene or gene block are shaded gray.
Figure 2 from: Yuhui X, Lijun Z, Yue H, Xiaoqi W, Chen Z, Huilun Z, Ruoran W, Da P, Hongying S (2017) Complete mitochondrial genomes from two species of Chinese freshwater crabs of the genus Sinopotamon recovered using next-generation sequencing reveal a novel gene order (Brachyura, Potamidae). ZooKeys 705: 41-60. https://doi.org/10.3897/zookeys.705.11852
Figure 2 - Phylogenetic analyses derived for brachyurans using the maximum likelihood (ML) analyses and Bayesian inferences (BI) using dataset A (13 PCGs) and dataset B (13 PCGs + two rRNAs). Branch lengths and topologies came from ML analysis. Values at the branches represent BP (Bootstrap value)/BPP (Bayesian posterior probability). 100/1.00 is denoted by an asterisk. The horizontal line stands for BP under 50 or BPP under 0.9 ML analyses. The gene rearrangement is denoted by the block on (A): (I) the translocation of trnH shared by the Brachyura taxa sampled; (II) the transposition of trnQ shared by potamid species; (III) the five-gene block, (trnM-nad2-trnW-trnC-trnY), translocation shared by three Sinopotamon crabs sampled.
Figure 5 from: Iturrieta-González I, Gené J, Guarro J, Castañeda-Ruiz RF, García D (2018) Neodendryphiella, a novel genus of the Dictyosporiaceae (Pleosporales). MycoKeys 37: 19-38. https://doi.org/10.3897/mycokeys.37.27275
Figure 5 - Dendryphiella variabilis sp. nov. (ex-type CBS 584.96). A–E Colonies on A PDA B PCA C SNA D OA E MEA at 25 °C after 14 d F Exudates and conidiophores produced on OA G–K Conidiophores and conidia. Scale bars: 50 µm (G–H), 10 µm (I–K).
Figure 4 from: Iturrieta-González I, Gené J, Guarro J, Castañeda-Ruiz RF, García D (2018) Neodendryphiella, a novel genus of the Dictyosporiaceae (Pleosporales). MycoKeys 37: 19-38. https://doi.org/10.3897/mycokeys.37.27275
Figure 4 - Neodendryphiella tarraconensis sp. nov. (ex-type FMR 16234). A–E Colonies on A PDA B PCA C SNA D OA E MEA at 25 °C after 14 d F–K Conidiophores and conidia. Scale bars:10 µm (G–K).
Figure 1 from: Iturrieta-González I, Gené J, Guarro J, Castañeda-Ruiz RF, García D (2018) Neodendryphiella, a novel genus of the Dictyosporiaceae (Pleosporales). MycoKeys 37: 19-38. https://doi.org/10.3897/mycokeys.37.27275
Figure 1 - Maximum Likelihood (ML) tree constructed with the ITS and LSU sequences of 30 strains representatives of different taxa in the families Dictyosporiaceae and Pleosporaceae . The phylogenetic tree was rooted with Paradendryphiella arenaria and P. salina . Bootstrap support values for ML greater than 70% and Bayesian posterior probabilities greater than 0.95 are given near nodes, respectively. Names of species newly described here are indicated in bold. Branch lengths are proportional to distance. T Ex-type strain.
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.