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.
8,819
datasets available to search
ShareScore release 0.9.0
Dataset results
8,819 results for “new data”
Figure 12 in Gorgocephalidae (Digenea: Lepocreadioidea) in the Indo-West Pacific: new species, life-cycle data and perspectives on species delineation over geographic range
Figure 12. Gorgocephalus euryaleae and Gorgocephalus graboides, scanning electron micrographs. A, B, oral suckers of adult Gorgocephalus euryaleae ex Kyphosus gladius, Point Peron, Rockingham, Western Australia. C, tegument of adult Gorgocephalus euryaleae, ex Kyphosus gladius, Point Peron. D, E, oral suckers of adult Gorgocephalus graboides ex Kyphosus cinerascens, Lizard Island, Queensland, Australia. F, tegument of adult Gorgocephalus graboides ex Kyphosus cinerascens, Lizard Island. Scale bars: A, E, 40 µm; B, D, 50 µm; C, F, 20 µm.
Data set for the paper "Temperatures and cooling rates recorded by the New Caledonia ophiolite: implications for cooling mechanisms in young forearc sequences"
<p>Data set for the paper "Temperatures and cooling rates recorded by the New Caledonia ophiolite: implications for cooling mechanisms in young forearc sequences" by Secchiari et al.</p>
Additional data, Table 2. — Forewing and proboscis lengths (cm) in Xanthopan praedicta stat. nov. – first 35 lines: MNHN specimens. – lines 36 (Ranomena) to 43 (Lakato): RCPB. – lines 44 (Ranomafana) to 47 (Amber Mountain): CJHL. – line 55 (female from Ranomafana) and last five lines: NHMUK. – last 30 lines: individuals captured and released by DCL, except for the six NHMUK specimens. in A new taxonomic status for Darwin's "predicted" pollinator: Xanthopan praedicta stat. nov. (Lepidoptera Sphingidae Sphinginae)
Additional data, Table 2. — Forewing and proboscis lengths (cm) in Xanthopan praedicta stat. nov. – first 35 lines: MNHN specimens. – lines 36 (Ranomena) to 43 (Lakato): RCPB. – lines 44 (Ranomafana) to 47 (Amber Mountain): CJHL. – line 55 (female from Ranomafana) and last five lines: NHMUK. – last 30 lines: individuals captured and released by DCL, except for the six NHMUK specimens.
Additional data, Table 1. — Forewing and proboscis lengths (cm) in Xanthopan morganii. – last four specimens: CJHL (Rungwe, Hombo, and Convalescence) and RCPB (Tsoundzou). – all other specimens: MNHN. in A new taxonomic status for Darwin's "predicted" pollinator: Xanthopan praedicta stat. nov. (Lepidoptera Sphingidae Sphinginae)
Additional data, Table 1. — Forewing and proboscis lengths (cm) in Xanthopan morganii. – last four specimens: CJHL (Rungwe, Hombo, and Convalescence) and RCPB (Tsoundzou). – all other specimens: MNHN.
Data to accompany 'New evidence suggests no sex bias in herbivory or plant defence'
<p><span><span><span><span><span><span><span><span><span><span><span>Dioecious plants can exhibit sexual dimorphism across a suite of plant traits, including susceptibility to herbivory and secondary chemistry. One hypothesis is that, due to greater costs of reproduction in females, males should grow faster and invest less in defense, resulting in male-biased herbivory. Indeed, a series of papers and a prominent meta-analysis have established male-biased herbivory as a robust result. However, more recent reviews have raised questions about how general the pattern is, citing the low breadth of taxon sampling. The literature on this topic has not been formally quantified by meta-analysis in over 15 years. Here we report the results of a meta-analysis of studies that measured sex bias in either herbivory and/or secondary defense in 71 dioecious plant species. We added 58 observations of herbivory and 41 of secondary chemistry to the original. We control for non-independence of effects from the same study and taxonomic group to address critiques of earlier studies. For secondary chemistry, we found no support for any consistent difference between male and female plants. For herbivory, results are directionally similar to earlier reports, although not statistically significant once we accounted for taxonomic group and study. We also found that the magnitude and direction of the effect of plant sex on herbivory declines, with earlier studies reporting a stronger male-bias. We discuss our results in light of the 'decline effect' and consider whether the datasets exhibit signs of evidence of the type(s) of biases that can result in declining effect sizes over time.</span></span></span></span></span></span></span></span></span></span></span></p>
FIGURE 6. Sonchus palustris—a in A new subgenus of Sonchus (Asteraceae: Cichorieae) inferred from molecular data
FIGURE 6. Sonchus palustris—a. carpopodium of the outermost achene, b. pappus bristles of the outermost achene, c. carpopodium of the inner achene, d. pappus bristles of the inner achene (Güzel 975 & Gültepe) / Sonchus erzincanicus—e. carpopodium of the outermost achene, f. pappus bristles of the outermost achene, g. carpopodium of the inner achene, h. pappus bristles of the inner achene (voucher Güzel 689 & Gültepe)
FIGURE 5. Sonchus palustris—a in A new subgenus of Sonchus (Asteraceae: Cichorieae) inferred from molecular data
FIGURE 5. Sonchus palustris—a. dorsal view of the outermost achene, b. dorsal view of the inner achene (Güzel 975& Gültepe) scale bar = 2 mm / Sonchus erzincanicus—c. dorsal view of the outermost achene, d. dorsal view of the inner achene, (voucher Güzel 689 & Gültepe) scale bar = 1 mm.
FIGURE 2 in A new subgenus of Sonchus (Asteraceae: Cichorieae) inferred from molecular data
FIGURE 2. Majority consensus phylogram of the subtribe Hyoseridinae from the BI analysis based on the matK dataset (support values: first-line MP jackknife, and ML bootstrap, second-line BI posterior probability, see Mejías et al. (2018) for details of the hidden clades, newly generated accessions and target groups are designated with blue color).
FIGURE 1 in A new subgenus of Sonchus (Asteraceae: Cichorieae) inferred from molecular data
FIGURE 1. Majority consensus phylogram of the subtribe Hyoseridinae from the BI analysis based on the nrITS dataset (support values: first-line MP jackknife, and ML bootstrap, second-line BI posterior probability, see Mejías et al. (2018) for details of the hidden clades, newly generated accessions and target groups are designated with blue color).
and) 33 () mm 4.4: lenght total (. nov. spec vulcanalis Metolinus.) Cuoco,) 32. (S): mm photo 3.5 (): 34 lenght () mm total 3.5 (:. nov lenght. spec total (lanceolatus) 1959,. P KRAATZ of Habitus (filum: 34 – 32 Xanthopius Figs in New data on the Oriental Xantholinini. 44. New species and new records from Nepal, Malaysia, Vietnam, Philippines, Sumatra, and Sabah (Coleoptera Staphylinidae)
and) 33 () mm 4.4: lenght total (. nov. spec vulcanalis Metolinus.) Cuoco,) 32. (S): mm photo 3.5 (): 34 lenght () mm total 3.5 (:. nov lenght. spec total (lanceolatus) 1959,. P KRAATZ of Habitus (filum: 34 – 32 Xanthopius Figs
◂Fig. 2 Maximum likelihood trees. A Tree obtained when analysing 18S data set. B Tree obtained when analysing 28S data set. C Tree obtained when analysing COI data set. D Tree obtained when analysing 16S data set. Bootstrap support values below nodes. Syllis and Typosyllis species as they were originally described in Ramisyllis kingghidorahi n. sp., a new branching annelid from Japan
◂Fig. 2 Maximum likelihood trees. A Tree obtained when analysing 18S data set. B Tree obtained when analysing 28S data set. C Tree obtained when analysing COI data set. D Tree obtained when analysing 16S data set. Bootstrap support values below nodes. Syllis and Typosyllis species as they were originally described
Raw data for "Field and Laboratory Assessment of a New Electrolytic Point-of-Use Water Treatment Technology"
<p>Within these files contains the raw data used for the Figures in "Field and Laboratory Assessment of a New Electrolytic Point-of-Use Water Treatment Technology."</p>
Data for: Thriving in a pandemic: determinants of excellent wellbeing among New Zealanders during the 2020 COVID-19 lockdown; a cross-sectional survey
<p><strong>Objective:</strong> The COVID-19 pandemic and associated restrictions are associated with adverse psychological impacts but an assessment of positive wellbeing is required to understand the overall impacts of the pandemic.</p> <p><strong>Methods: </strong>The NZ Lockdown Psychological Distress Survey measured excellent wellbeing categorised by a WHO-Five Well-being Index (WHO-5) score ≥22. The survey also contained demographic and pre-lockdown questions, subjective and objective lockdown experiences, and questions on alcohol use. The proportion of participants with excellent wellbeing is reported with multivariate analysis examining the relative importance of individual factors associated with excellent wellbeing.</p> <p><strong>Results:</strong> Approximately 9% of the overall sample reported excellent wellbeing during the New Zealand lockdown. Excellent wellbeing status was associated with older age, male gender, Māori and Asian ethnicity, and lower levels of education. Excellent wellbeing was negatively associated with smoking, poor physical and mental health, and previous trauma.</p> <p><strong>Conclusion:</strong> A substantial minority of New Zealanders reported excellent wellbeing during severe COVID-19 pandemic restrictions. Demographic and broader health factors predicted excellent wellbeing status. An understanding of these factors may help to enhance wellbeing during any future lockdowns.</p>
FIGURE. Phylogenetic tree of specimens on Poaceae and related host plants constructed by MP method based on ITS+28S regions of rDNA. Bootstrap values of MP and ML are followed by the Bayesian posterior probabilities (Bpp) on the nodes in the topology. Asterisk (*) represents bootstrap values or Bpp less than 50% in the topology. Sample data are shown with voucher specimen number or GenBank accession number, and host plant. Sequence data determined in this study are shown in color. Teliospore shapes are shown in each clade detected, and new species are shown by asterisk (*) on clades. 0, I: Spermogonial and aecial host genus. Asterisk (*) on host plants: Spermogonial and aecial host plants. in Phylogenetic approach for identification and life cycles of Puccinia (Pucciniaceae) species on Poaceae from northeastern China
FIGURE. Phylogenetic tree of specimens on Poaceae and related host plants constructed by MP method based on ITS+28S regions of rDNA. Bootstrap values of MP and ML are followed by the Bayesian posterior probabilities (Bpp) on the nodes in the topology. Asterisk (*) represents bootstrap values or Bpp less than 50% in the topology. Sample data are shown with voucher specimen number or GenBank accession number, and host plant. Sequence data determined in this study are shown in color. Teliospore shapes are shown in each clade detected, and new species are shown by asterisk (*) on clades. 0, I: Spermogonial and aecial host genus. Asterisk (*) on host plants: Spermogonial and aecial host plants.
Data from: Late Cretaceous European theropod palaeobiodiversity, palaeobiogeography and the intra-Maastrichtian faunal turnover: new contributions from the Iberian fossil site of Laño
<p>A total of 227 theropod teeth have so far been recovered from the late Campanian Laño site (northern Iberian Peninsula). The teeth were studied for their qualitative and quantitative features. From the theropod sample found at Laño, seven morphotypes attributed to five taxa are identified: a medium to large abelisaurid (<i>Arcovenator</i> sp.) and four small coelurosaurians (Dromaeosauridae indet., Paraves indet., cf. <i>Paronychodon</i> sp. and cf. <i>Richardoestesia</i> sp.). Together with the ground bird <i>Gargantuavis</i> and a possible ornithomimosaur, the theropod fauna of Laño might be composed of two medium- to large-sized non-avian theropods, four small-bodied non-avian theropods and a large terrestrial bird. This makes the Laño site the richest and most diverse latest Cretaceous theropod site of Europe. Furthermore, the Laño site and the Late Cretaceous localities of Europe that have yielded theropod remains suggest that the medium- to large-sized theropods were abelisaurids or indeterminate theropods. The small theropods are more abundant, diverse and represented by different dromaeosaurids, <i>Paronychodon</i>, <i>Richardoestesia</i>, or related forms, troodontids and, probably, by other paravians. Among birds, enantiornithines, gargantuaviids and ornithurines are also common in the European Late Cretaceous sites. The theropod assemblage of Laño, together with the taxa of other Late Cretaceous sites, supports the idea that several theropod dispersal events took place during the Cretaceous. This resulted in a mixture of European endemic, Asiamerican and Gondwanan forms. This study also supports the hypothesis that the intra-Maastrichtian faunal turnover that occurred in the Ibero-Armorican landmass seems to have had no effect on theropods.</p>
Data from: A new lineage of Galapagos giant tortoises identified from museum samples
<p>The Galapagos Archipelago is recognized as a natural laboratory for studying evolutionary processes. San Cristóbal was one of the first islands colonized by tortoises, which radiated from there across the archipelago to inhabit 10 islands. Here, we sequenced the mitochondrial control region from six historical giant tortoises from San Cristóbal (five long deceased individuals found in a cave and one found alive during an expedition in 1906) and discovered that the five from the cave are from a clade that is distinct among known Galapagos giant tortoises but closely related to the species from Española and Pinta Islands. The haplotype individual collected alive in 1906 is in the same clade as the haplotype in the contemporary population. To search for traces of a second lineage in the contemporary population on San Cristóbal, we closely examined the population by sequencing the mitochondrial control region for 129 individuals and genotyping 70 of these for both 21 microsatellite loci and >12 000 genome-wide single nucleotide polymorphisms [SNPs]. The dataset archived here consists of a VCF file of the SNPs genotyped through ddRAD and a structure file of the 21 microsatellites with the genotypes for the same 64 individuals in each. Only a single mitochondrial haplotype was found, with no evidence to suggest substructure based on the nuclear markers.</p>
FIGURE 6. Hyphinomos svenhedini Ramme, 1950 in Revision of the high-altitude genus Hyphinomos Uvarov, 1921 (Orthoptera: Tettigoniidae) with a redescription and new data on mating behavior and acoustic signals of H. svenhedini Ramme, 1950
FIGURE 6. Hyphinomos svenhedini Ramme, 1950 (A) female head, pronotum and forewing, (B) male head, pronotum and forewing, (C) maxillary palpi, (D) female head and pronotum, (E) front view of face and (F) top view of fore tibia showing external and internal tympanum. Scale 5mm.
FIGURE 1 in Revision of the high-altitude genus Hyphinomos Uvarov, 1921 (Orthoptera: Tettigoniidae) with a redescription and new data on mating behavior and acoustic signals of H. svenhedini Ramme, 1950
FIGURE 1. Map showing type localities of Hyphinomos fasciata Uvarov, 1921 (in Dakar, Western Tibet, China) and H. svenhedini Ramme, 1950 (in Hanle, Indus Valley, Ladakh and Lahaul, Himachal Pradesh, India). Zanskar and Shashi lake, Kargil, Ladakh are additional locations from where H. svenhedini has been reported. Area highlighted in green is Ladakh, U.T., pink: Kargil district of Ladakh, blue: Lahaul and Spiti district in Himachal Pradesh.
FIGURE 12 in Revision of the high-altitude genus Hyphinomos Uvarov, 1921 (Orthoptera: Tettigoniidae) with a redescription and new data on mating behavior and acoustic signals of H. svenhedini Ramme, 1950
FIGURE 12. Male and female of Hyphinomos svenhedini Ramme, 1950 (A) exhibiting end-to-end copulation position in laboratory condition and (B) in natural habitat.
FIGURE 5. Hyphinomos svenhedini Ramme, 1950 in Revision of the high-altitude genus Hyphinomos Uvarov, 1921 (Orthoptera: Tettigoniidae) with a redescription and new data on mating behavior and acoustic signals of H. svenhedini Ramme, 1950
FIGURE 5. Hyphinomos svenhedini Ramme, 1950 (A & B) female and (C & D) male in dorsal and lateral view respectively. Scale 14mm.
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.