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.
2,531
datasets available to search
ShareScore release 0.9.0
Dataset results
2,531 results for “New combination”
Figure 3 from: Yang L-H, Wen F, Kong H-H, Sun Z-X, Su L-Y, Kang M (2020) Two new combinations in Oreocharis (Gesneriaceae) based on morphological, molecular and cytological evidence. In: Shui Y-M, Chen W-H, Ren M-X, Wen F, Hong X, Qiu Z-J, Wei Y-G, Kang M (Eds) Taxonomy of Gesneriaceae in China and Vietnam. PhytoKeys 157: 43-58. https://doi.org/10.3897/phytokeys.157.32609
Figure 3 Bayesian (> 50%) tree resulting of the combined nuclear (ITS) and plastid (trnL-F) data matrices. Posterior probability (PP) from the BI analysis are indicated above branches and Bootstrap value (BS) from the ML analysis are indicated below. The asterisk indicates a BS < 50. The dash indicates the topological discordance between ML and Bayesian tree. The two species, O. baolianis and O. guileana, are highlighted in bold.
Figure 1 from: Yang L-H, Wen F, Kong H-H, Sun Z-X, Su L-Y, Kang M (2020) Two new combinations in Oreocharis (Gesneriaceae) based on morphological, molecular and cytological evidence. In: Shui Y-M, Chen W-H, Ren M-X, Wen F, Hong X, Qiu Z-J, Wei Y-G, Kang M (Eds) Taxonomy of Gesneriaceae in China and Vietnam. PhytoKeys 157: 43-58. https://doi.org/10.3897/phytokeys.157.32609
Figure 1 Photographs of Oreocharis guileana (A–H), O. pilosopetiolata (I), Boeica ferruginea (J) and Beccarinda tonkinensis (K). A, E, I habit B, C flower D opened corolla, showing stamens and staminodes F pistil G, H, J, K mature fruit.
Figure 4 from: Yang L-H, Wen F, Kong H-H, Sun Z-X, Su L-Y, Kang M (2020) Two new combinations in Oreocharis (Gesneriaceae) based on morphological, molecular and cytological evidence. In: Shui Y-M, Chen W-H, Ren M-X, Wen F, Hong X, Qiu Z-J, Wei Y-G, Kang M (Eds) Taxonomy of Gesneriaceae in China and Vietnam. PhytoKeys 157: 43-58. https://doi.org/10.3897/phytokeys.157.32609
Figure 4 Somatic metaphase chromosome spreads of Oreocharis guileana, 2n = 34 (A), O. baolianis, 2n = 34 (B), Beccarinda tonkinensis, 2n = 20 (C) and Boeica stolonifera, 2n = 20 (D). Scale bar: 10 μm.
Figure 2 from: Yang L-H, Wen F, Kong H-H, Sun Z-X, Su L-Y, Kang M (2020) Two new combinations in Oreocharis (Gesneriaceae) based on morphological, molecular and cytological evidence. In: Shui Y-M, Chen W-H, Ren M-X, Wen F, Hong X, Qiu Z-J, Wei Y-G, Kang M (Eds) Taxonomy of Gesneriaceae in China and Vietnam. PhytoKeys 157: 43-58. https://doi.org/10.3897/phytokeys.157.32609
Figure 2 Photographs of Oreocharis baolianis. A–C Habit D, E flower F, H opened corolla, showing stamens and staminodes G anthers I pistil J mature fruit.
Figure 3 from: Zhao W-Y, Fritsch PW, Liu Z-C, Fan Q, Jin J-H, Liao W-B (2020) New combinations and synonyms in Rehderodendron (Styracaceae). PhytoKeys 161: 79-88. https://doi.org/10.3897/phytokeys.161.54970
Figure 3 A lectotype of Rehderodendron macrophyllum (Yu Ping-Hua s.n. [KUN (acc. # KUN0026237)] B isotype of R. truongsonense (Ulf Swenson, Do Van Truong, Hoang Manh Quyen & Sylvain Razaflimandimbison 2131 [P00937133]).
Figure 2 from: Zhao W-Y, Fritsch PW, Liu Z-C, Fan Q, Jin J-H, Liao W-B (2020) New combinations and synonyms in Rehderodendron (Styracaceae). PhytoKeys 161: 79-88. https://doi.org/10.3897/phytokeys.161.54970
Figure 2 Inflorescences of Rehderodendron burmanicum, Pterostyrax corymbosus Siebold & Zucc. and R. microcarpum. A inflorescence of R. burmanicum, showing flowering shoots comprising only inflorescences, flowers not strictly arranged on one side of ultimate inflorescence branches and (red arrow) stamens longer than the petals B inflorescence of P. corymbosus, showing flowering shoots comprising both inflorescences and (red arrow) leaves and flowers arranged on one side of ultimate inflorescence branches C inflorescences of R. microcarpum, showing flowering shoots comprising only inflorescences, flowers not strictly arranged on one side of ultimate inflorescence branches and stamens that are shorter than the petals. (Photographs: A from the holotype of R. burmanicumB by Wan-Yi Zhao from Jinggangshan, Jiangxi, China C by Wan-Yi Zhao from Gongshan, Yunnan, China).
Figure 4 from: Zhao W-Y, Fritsch PW, Liu Z-C, Fan Q, Jin J-H, Liao W-B (2020) New combinations and synonyms in Rehderodendron (Styracaceae). PhytoKeys 161: 79-88. https://doi.org/10.3897/phytokeys.161.54970
Figure 4 Morphology of Rehderodendron macrophyllum and R. macrocarpum Hu. A–DRehderodendron macrophyllumA branchlet and leaf B fruiting branch C young fruit D transverse section of fruit showing endocarp with many rays intruding into the mesocarp E fruit transverse section of R. macrocarpum. (Photographs: A–D by Wan-Yi Zhao from Hekou, Yunnan, China E by Wan-Yi Zhao rom Wawushan, Sichuan, China).
Figure 1 from: Martins AL, Melo GAR (2020) Revision of the fossil species of Thaumatodryinus Perkins from Dominican amber, with a new combination and description of a new species (Hymenoptera, Dryinidae). Journal of Hymenoptera Research 79: 77-88. https://doi.org/10.3897/jhr.79.57686
Figure 1 †Thaumatodryinus fuscescens sp. nov., female holotype. A habitus, dorsal view B right antenna, dorsal view C head and mesosoma, antero-ventral view D head and mesosoma, dorsal view E apical portion of flagellum, with details of flagellomeres 5–8 F–G Apical portion of fore leg, with details of the chela. Scale bars: 2 mm (A), 0.5 mm (B), 0.5 mm (C–D), 0.3 mm (E–G).
Figure 3 from: Martins AL, Melo GAR (2020) Revision of the fossil species of Thaumatodryinus Perkins from Dominican amber, with a new combination and description of a new species (Hymenoptera, Dryinidae). Journal of Hymenoptera Research 79: 77-88. https://doi.org/10.3897/jhr.79.57686
Figure 3 †Thaumatodryinus priscus (Olmi, 1998), female holotype. A habitus, lateral view B habitus, ventral view C head and mesosoma, lateral view D head and mesosoma, dorsal view E head and mesosoma, ventral view F apical portion of fore leg, with details of the chela. Scales: 1 mm (A), 1 mm (B), 0.5 mm (C), 0.5 mm (D–F).
Figure 2 from: Martins AL, Melo GAR (2020) Revision of the fossil species of Thaumatodryinus Perkins from Dominican amber, with a new combination and description of a new species (Hymenoptera, Dryinidae). Journal of Hymenoptera Research 79: 77-88. https://doi.org/10.3897/jhr.79.57686
Figure 2 †Thaumatodryinus miocenicus Olmi, 1995, female holotype. A habitus, dorsal view B habitus, ventral view C habitus, lateral view D habitus, dorsal view E head and mesosoma, ventral view F habitus, lateral view. Scale bars: 1 mm (A–C), 1 mm (D, F), 1 mm (E).
FIGURE 2 in Synopsis of the Asian species in the genus Zarcosia Collado & Alonso-Zarazaga 1996 with new combinations and descriptions of fourteen new species
FIGURE 2. continued next page.
FIGURE 4 in Emesis planeca n. comb. (Lepidoptera: Riodinidae): a new combination revealed by molecular evidence with a description of its morphological variation
FIGURE 4. Male labial palpus and latero - ventral view of the head of Emesis planeca n. comb.
FIGURES 31–32 in The genusParascepsis Dognin,1923(Lepidoptera,Erebidae,Arctiinae,Ctenuchina) in Peru, with the description of three new species, a new combination and their geographical distributions
FIGURES 31–32. Wings of Parascepsis lantigni Grados new species. 31. Forewing. 32 Hindwing.
FIGURES 7–8 in The genusParascepsis Dognin,1923(Lepidoptera,Erebidae,Arctiinae,Ctenuchina) in Peru, with the description of three new species, a new combination and their geographical distributions
FIGURES 7–8. Wings of Parascepsis solox (Dognin). 7. Forewing. 8. Hindwing.
FIGURES 19–20 in The genusParascepsis Dognin,1923(Lepidoptera,Erebidae,Arctiinae,Ctenuchina) in Peru, with the description of three new species, a new combination and their geographical distributions
FIGURES 19–20. Wings of Parascepsis ockendeni Rothschild. 19. Forewing. 20. Hindwing.
Data from: Combining noninvasive genetics and a new mammalian sex-linked marker provides new tools to investigate population size, structure and individual behaviour: an application to bats
Monitoring wild populations is crucial for their effective management. Noninvasive genetic methods provide robust data from individual free-ranging animals, which can be used in capture-mark-recapture (CMR) models to estimate demographic parameters without capturing or disturbing them. However, sex- and status-specific behaviour, which may lead to differences in detection probabilities, is rarely considered in monitoring. Here, we investigated population size, sex ratio, sex- and status-related behaviour in 19 Rhinolophus hipposideros maternity colonies (Northern France) with a noninvasive genetic CMR approach (using faeces) combined with parentage assignments. The use of the DDX3X/Y-Mam sexual marker designed in this study, which shows inter- and intra-chromosomal length polymorphism across placental mammals, together with 8 polymorphic microsatellite markers, produced high quality genetic data with limited genotyping errors and allowed us to reliably distinguish different categories of individuals (males, reproductive and non-reproductive females) and to estimate population sizes. We showed that visual counts represent well adult female numbers and that population composition in maternity colonies changes dynamically during the summer. Before parturition, colonies mainly harbour pregnant and non-pregnant females with a few visiting males whereas after parturition, colonies are mainly composed of mothers and their offspring with a few visiting non-mothers and males. Our approach gives deeper insight into sex- and status-specific behaviour, a prerequisite for understanding population dynamics and developing effective monitoring and management strategies. Provided sufficient samples can be obtained, this approach can be readily applied to a wide range of species.
FIGURE 2 in Long-legged flies (Diptera: Dolichopodidae) in the collection of the Natal Museum: A review of C. H. Curran's types, new synonyms, and new combinations
FIGURE 2. Acropsilus vorax (Curran), hypopygium, left lateral view. Scale bar: 0.1 mm
FIGURE 1 in Long-legged flies (Diptera: Dolichopodidae) in the collection of the Natal Museum: A review of C. H. Curran's types, new synonyms, and new combinations
FIGURE 1. Acropsilus vorax (Curran), wing. Scale bar: 0.5 mm.
FIGURE 1. Typhlocharis toletana n in A new Typhlocharis (Coleoptera: Carabidae: Anillina) from Spain: combining adult and larval morphological data with DNA information
FIGURE 1. Typhlocharis toletana n. sp., adult, habitus, dorsal view, total body length 1.2 mm.
FIGURE 11 in Status of Batakomacrus Kolarov (Hymenoptera: Ichneumonidae: Orthocentrinae), with new generic combinations and description of a new species
FIGURE 11. The same, ovipositor sheaths.
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.