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2,576 results for “host species”
Figure 28 in Acmaeodera (Coleoptera: Buprestidae): A new species of Acmaeodera Eschscholtz, 1829 from the southwestern United States, with three new synonymies, new state and host records, and a key to species occurring east of the Rocky Mountain states
Figure 28. Acmaeodera opuntiae Knull.
Figure 36 in Acmaeodera (Coleoptera: Buprestidae): A new species of Acmaeodera Eschscholtz, 1829 from the southwestern United States, with three new synonymies, new state and host records, and a key to species occurring east of the Rocky Mountain states
Figure 36. Acmaeodera quadrivittatoides Nelson and Westcott.
Figure 19 in Acmaeodera (Coleoptera: Buprestidae): A new species of Acmaeodera Eschscholtz, 1829 from the southwestern United States, with three new synonymies, new state and host records, and a key to species occurring east of the Rocky Mountain states
Figure 19. Acmaeodera maculifera Horn.
Figure 34 in Acmaeodera (Coleoptera: Buprestidae): A new species of Acmaeodera Eschscholtz, 1829 from the southwestern United States, with three new synonymies, new state and host records, and a key to species occurring east of the Rocky Mountain states
Figure 34. Acmaeodera princeps Kerremans.
Figure 16 in Acmaeodera (Coleoptera: Buprestidae): A new species of Acmaeodera Eschscholtz, 1829 from the southwestern United States, with three new synonymies, new state and host records, and a key to species occurring east of the Rocky Mountain states
Figure 16. Acmaeodera haemorrhoa LeConte.
Figure 27 in Acmaeodera (Coleoptera: Buprestidae): A new species of Acmaeodera Eschscholtz, 1829 from the southwestern United States, with three new synonymies, new state and host records, and a key to species occurring east of the Rocky Mountain states
Figure 27. Acmaeodera opacula Horn.
Figure 6 in Acmaeodera (Coleoptera: Buprestidae): A new species of Acmaeodera Eschscholtz, 1829 from the southwestern United States, with three new synonymies, new state and host records, and a key to species occurring east of the Rocky Mountain states
Figure 6. Acmaeodera auritincta Fall.
Figure 32 in Acmaeodera (Coleoptera: Buprestidae): A new species of Acmaeodera Eschscholtz, 1829 from the southwestern United States, with three new synonymies, new state and host records, and a key to species occurring east of the Rocky Mountain states
Figure 32. Acmaeodera parkeri Cazier.
Figure 22 in Acmaeodera (Coleoptera: Buprestidae): A new species of Acmaeodera Eschscholtz, 1829 from the southwestern United States, with three new synonymies, new state and host records, and a key to species occurring east of the Rocky Mountain states
Figure 22. Acmaeodera mixta LeConte.
Figure 14 in Acmaeodera (Coleoptera: Buprestidae): A new species of Acmaeodera Eschscholtz, 1829 from the southwestern United States, with three new synonymies, new state and host records, and a key to species occurring east of the Rocky Mountain states
Figure 14. Acmaeodera gibbula LeConte.
Figure 26 in Acmaeodera (Coleoptera: Buprestidae): A new species of Acmaeodera Eschscholtz, 1829 from the southwestern United States, with three new synonymies, new state and host records, and a key to species occurring east of the Rocky Mountain states
Figure 26. Acmaeodera obtusa Horn.
Figure 5 in Acmaeodera (Coleoptera: Buprestidae): A new species of Acmaeodera Eschscholtz, 1829 from the southwestern United States, with three new synonymies, new state and host records, and a key to species occurring east of the Rocky Mountain states
Figure 5. Acmaeodera amplicollis Leconte.
Figure 31 in Acmaeodera (Coleoptera: Buprestidae): A new species of Acmaeodera Eschscholtz, 1829 from the southwestern United States, with three new synonymies, new state and host records, and a key to species occurring east of the Rocky Mountain states
Figure 31. Acmaeodera paradisjuncta Knull.
Figure 23 in Acmaeodera (Coleoptera: Buprestidae): A new species of Acmaeodera Eschscholtz, 1829 from the southwestern United States, with three new synonymies, new state and host records, and a key to species occurring east of the Rocky Mountain states
Figure 23. Acmaeodera natlovei, new species.
Figure 13 in Acmaeodera (Coleoptera: Buprestidae): A new species of Acmaeodera Eschscholtz, 1829 from the southwestern United States, with three new synonymies, new state and host records, and a key to species occurring east of the Rocky Mountain states
Figure 13. Acmaeodera flavopicta Waterhouse.
Figure 9 in Acmaeodera (Coleoptera: Buprestidae): A new species of Acmaeodera Eschscholtz, 1829 from the southwestern United States, with three new synonymies, new state and host records, and a key to species occurring east of the Rocky Mountain states
Figure 9. Acmaeodera cribricollis Horn.
Figure 8 in Acmaeodera (Coleoptera: Buprestidae): A new species of Acmaeodera Eschscholtz, 1829 from the southwestern United States, with three new synonymies, new state and host records, and a key to species occurring east of the Rocky Mountain states
Figure 8. Acmaeodera consors Horn.
Figure 21 in Acmaeodera (Coleoptera: Buprestidae): A new species of Acmaeodera Eschscholtz, 1829 from the southwestern United States, with three new synonymies, new state and host records, and a key to species occurring east of the Rocky Mountain states
Figure 21. Acmaeodera miliaris Horn.
Data from: Genome-wide support for incipient Tula orthohantavirus species within a single rodent host lineage
<p>Evolutionary divergence of viruses is most commonly driven by co-divergence with their hosts or through isolation of transmission after host-shifts. It remains mostly unknown, however, whether divergent phylogenetic clades within named virus species represent functionally equivalent byproducts of high evolutionary rates or rather incipient virus species. Here, we test these alternatives with genomic data from two widespread phylogenetic clades in Tula orthohantavirus (TULV) within a single evolutionary lineage of their natural rodent host, the common vole Microtus arvalis. We examined voles from 42 locations in the contact region between clades for TULV infection by RT-PCR. Sequencing yielded 23 TULV Central North and 21 TULV Central South genomes which differed by 14.9-18.5% at the nucleotide and 2.2-3.7% at the amino acid level without evidence of recombination or reassortment. Geographic cline analyses demonstrated an abrupt (<1 km wide) transition between the parapatric TULV clades in continuous landscape. This transition was located within the Central mitochondrial lineage of M. arvalis and genomic SNPs showed gradual mixing of host populations across it. Genomic differentiation of hosts was much weaker across the TULV Central North to South transition than across the nearby hybrid zone between two evolutionary lineages in the host. We suggest that these parapatric TULV clades represent functionally distinct, incipient species which are likely differently affected by genetic polymorphisms in the host. This highlights the potential of natural viral contact zones as systems for investigating of the genetic and evolutionary factors enabling or restricting the transmission of RNA viruses.</p>
Foliar endophyte diversity in eastern Asia-eastern North America disjunct tree species – Influences of host identity, environment, phylogeny, and geographic isolation
<p><span>The well-known eastern Asia (EA) and eastern North America (ENA) floristic disjunction provides a unique system for biogeographic and evolutionary studies. Despite considerable interest in the disjunction, few studies have investigated the patterns and their underlying drivers of allopatric divergence in sister species or clades isolated in the two areas. Endophyte diversity and assembly in disjunct sister taxa, as an ecological trait, may have played an important role in the processes of allopatric evolution, but no studies have examined endophytes in these disjunct lineages. In this study, we compared foliar endophytes (including both fungi and bacteria) in 17 EA-ENA disjunct species pairs from genera representing conifers and major clades of angiosperms, as well as 23 species of </span><em>Cornus</em> from the US and China. We sequenced the ITS of fungi and 16S rDNA of bacteria to understand the composition of the endophyte community and gain insights into the relative roles of geographic isolation, host identity, phylogeny, and environment in shaping endophytic diversity patterns. We detected a much richer fungal than bacterial community in leaves of all species. Beta diversity varied greatly among individuals within species, between species, among genera, and among three natural environmental conditions. Based on a principal coordinates analysis, we found no close clustering of endophyte communities in samples from the same host plant species, from the same genus, or from the same geographic origin (i.e. EA or ENA) (when plants were grown in the same common garden), but we did detect clustering of samples from plants grown in the same environment (i.e., same geographic location). We observed separation of microbes in plant samples of the same species grown in different locations/environments. However, pooled samples across all species from the common garden with the same geographic origin (EA vs. ENA) showed a moderate level of dissimilarity in fungal endophytes between EA and ENA. An overall significant correlation between endophyte community dissimilarity and phylogenetic distance was detected among the disjunct genera but not among species of <em>Cornus</em>. However, significant correlation between order, family, and genera of endophytes and phylogenetic distance of Cornus species was observed. We also found no significant differences in Foliar Endophytic Fungal (FEF) communities between counterparts of disjunct species pairs in EA and ENA in most genera except in <em>Liriodendron</em> and <em>Cornus</em>, although the beta diversity within genera is high. Our results suggest important roles of host identity and environment (geographic locations), and a likely minor role of phylogenetic divergence and biogeographic isolation in shaping the pattern of foliar endophyte diversity and assembly in the EA-ENA disjunct genera, as well as in <em>Cornus</em>. The results further suggest that the sister taxa in EA and ENA are likely different in their foliar endophyte composition when growing in their native habitats due to differences in geographic locations and local environments, which is potentially a factor driving allopatric divergence of species functional features. This hypothesis can be tested by analysis of samples from native habitats.</p>
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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.