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261
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ShareScore release 0.9.0
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261 results for “hypothesis testing”
Data from: Testing the reproductive groundplan hypothesis in ants (Hymenoptera: Formicidae)
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Data from: Testing the Münch hypothesis of long distance phloem transport in plants
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Data from: A test of the hypothesis that correlational selection generates genetic correlations
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Data from: Behavioural mediators of genetic life-history trade-offs: a test of the pace-of-life syndrome hypothesis in field crickets
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Data from: Testing the correlated response hypothesis for the evolution and maintenance of male mating preferences in Drosophila serrata
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Aquaplanet experiment data for Webb, M. J., & Lock, A. P. (2020). Testing a physical hypothesis for the relationship between climate sen-sitivity and double-ITCZ bias in climate models.Journal of Advances in Modeling Earth Systems, 12,e2019MS001999.https://doi.org/10.1029/2019MS001999
<p><strong>Aquaplanet experiment data from Webb and Lock (2020)</strong></p> <p><br> Webb, M. J., & Lock, A. P. (2020). Testing a physical hypothesis for the relationship between climate sen-sitivity and double-ITCZ bias in climate models.Journal of Advances in Modeling Earth Systems, 12,e2019MS001999.https://doi.org/10.1029/2019MS001999</p> <p>CSV files containing data from Figs 1(b) and 2(a-d)</p> <p>Figure 2b:</p> <p>APEQ.Precipitation_mmperday.zonal.csv<br> APEQ_2LW_Cloud.Precipitation_mmperday.zonal.csv<br> APEQ_3LW_Cloud.Precipitation_mmperday.zonal.csv</p> <p>Figure 3a:</p> <p>APEQ.w700.zonal.csv<br> APEQ_3LW_Cloud.w700.zonal.csv<br> APEQ_2LW_Cloud.w700.zonal.csv</p> <p>Figure 3b:</p> <p>APEQ.Estimated_Inversion_Strength_K.zonal.csv<br> APEQ_2LW_Cloud.Estimated_Inversion_Strength_K.zonal.csv<br> APEQ_3LW_Cloud.Estimated_Inversion_Strength_K.zonal.csv</p> <p>Figure 3c:</p> <p>APEQ.Net_CRE_Wperm2.zonal.csv<br> APEQ_2LW_Cloud.Net_CRE_Wperm2.zonal.csv<br> APEQ_3LW_Cloud.Net_CRE_Wperm2.zonal.csv</p> <p>Figure 3d:</p> <p>APEQ4K-APEQ.Net_CRE_Feedback_Wperm2perK.zonal.csv<br> APEQ4K_2LW_Cloud-APEQ_2LW_Cloud.Net_CRE_Feedback_Wperm2perK.zonal.csv<br> APEQ4K_3LW_Cloud-APEQ_3LW_Cloud.Net_CRE_Feedback_Wperm2perK.zonal.csv</p> <p>Any queries please contact Mark Webb mark.webb@metoffice.gov.uk</p> <p> </p>
Data from: Testing the niche breadth-range size hypothesis: habitat specialization versus performance in Australian alpine daisies
Relatively common species within a clade are expected to perform well across a wider range of conditions than their rarer relatives, yet experimental tests of this "niche breadth—range size" hypothesis remain surprisingly scarce. Rarity may arise due to trade-offs between specialization and performance across a wide range of environments. Here we use common garden and reciprocal transplant experiments to test the niche breadth—range size hypothesis, focusing on four common and three rare endemic alpine daisies (Brachyscome spp.) from the Australian Alps. We used three experimental contexts: 1) alpine reciprocal seedling experiment: a test of seedling survival and growth in three alpine habitat types differing in environmental quality and species diversity, 2) warm environment common garden: a test of whether common daisy species have higher growth rates and phenotypic plasticity, assessed in a common garden in a warmer climate and run simultaneously with experiment 1, and 3) alpine reciprocal seed experiment: a test of seed germination capacity and viability in the same three alpine habitat types as in experiment 1. In the alpine reciprocal seedling experiment, survival of all species was highest in the open heathland habitat where overall plant diversity is high, suggesting a general, positive response to a relatively productive, low-stress environment. We found only partial support for higher survival of rare species in their habitats of origin. In the warm environment common garden, three common daisies exhibited greater growth and biomass than two rare species, but the other rare species performed as well as the common species. In the alpine reciprocal seed experiment, common daisies exhibited higher germination across most habitats, but rare species maintained a higher proportion of viable seed in all conditions, suggesting different life history strategies. These results indicate that some but not all rare, alpine endemics exhibit stress tolerance at the cost of reduced growth rates in low-stress environments compared to common species. Finally, these findings suggest the seed stage is important in the persistence of rare species, and they provide only weak support at the seedling stage for the niche breadth-range size hypothesis.
Testing the Adipose Expandability Hypothesis in Vivo During Overfeeding
ClinicalTrials.gov study NCT04583514. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Testing the Noradrenergic Hypothesis of Transcutaneous Vagus Nerve Stimulation
ClinicalTrials.gov study NCT04455295. IPD Sharing: NO. Countries: 1. Publications: 0.
Data from: Testing the niche breadth-range size hypothesis: habitat specialization versus performance in Australian alpine daisies
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A test of the pioneer factor hypothesis using ectopic liver gene activation [0.05dox CUTTag]
GEO Series GSE189006. Homo sapiens. 4 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
A test of the pioneer factor hypothesis using ectopic liver gene activation
GEO Series GSE182191. Homo sapiens. 48 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
A test of the pioneer factor hypothesis using ectopic liver gene activation [0.05dox RNAseq]
GEO Series GSE189020. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
A test of the pioneer factor hypothesis using ectopic liver gene activation [ATACseq]
GEO Series GSE182188. Homo sapiens. 12 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
A test of the pioneer factor hypothesis using ectopic liver gene activation [RNAseq]
GEO Series GSE182190. Homo sapiens. 18 samples. Type: Expression profiling by high throughput sequencing.
A test of the pioneer factor hypothesis using ectopic liver gene activation [CUTTag]
GEO Series GSE182189. Homo sapiens. 8 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Figures 128–135 in Phylogeny of Neotropical Castniinae (Lepidoptera: Cossoidea: Castniidae): testing the hypothesis of the mimics as a monophyletic group and implications for the arrangement of the genera
Figures 128–135. Female genitalia and associated characters, dorsal view: 128, Synpalamides amycus (Cramer [1779]) comb. nov.; 129, Yagra fonscolombe (Godart, [1824]); 130, Athis inca (Walker, 1854); 131, Athis palatinus (Cramer, 1777); 132, Telchin syphax (Fabricius, 1775); 133, Imara therapon (Kollar, 1839) comb. nov.; 134, Synpalamides fabricii (Swainson, 1823) comb. nov.; 135, Castnia invaria Walker, 1854. Scale bar: 1 mm.
Figures 111–116 in Phylogeny of Neotropical Castniinae (Lepidoptera: Cossoidea: Castniidae): testing the hypothesis of the mimics as a monophyletic group and implications for the arrangement of the genera
Figures 111–116. Female genitalia and associated characters, dorsal view: 111, Imara acraeoides (Guérin-Ménéville, [1832]) comb. nov.; 112, Synpalamides amycus (Cramer [1779]) comb. nov.; 113, Castnius marcus (Jordan, 1908); 114, Castnia invaria Walker, 1854; 115, Prometheus cochrus (Fabricius, 1787); 116, Ceretes marcelserres (Godart, [1824]). Scale bars: 1 mm.
Figures 49–51 in Phylogeny of Neotropical Castniinae (Lepidoptera: Cossoidea: Castniidae): testing the hypothesis of the mimics as a monophyletic group and implications for the arrangement of the genera
Figures 49–51. Wing scales: 49, piliform scales on the hindwing base of Imara pallasia (Eschscholtz, 1821); 50, oblong scales on the hindwing of Yagra fonscolombe (Godart, [1824]); 51, projection on the inner margin of the forewing with oblong scales of Synpalamides amycus (Cramer [1779]) comb. nov. Scale bars: 1 cm.
Figures 87–95 in Phylogeny of Neotropical Castniinae (Lepidoptera: Cossoidea: Castniidae): testing the hypothesis of the mimics as a monophyletic group and implications for the arrangement of the genera
Figures 87–95. Tegumen, uncus, and associated characters, dorsal view: 87, Yagra dalmannii (Gray, 1838); 88, Synpalamides ctesiphon (Hübner, [1820]) comb. nov.; 89, Prometheus heliconioides (Herrich-Schäffer, [1853]) comb. nov.; 90, Telchin atymnius (Dalman, 1824); 91, Castnia invaria Walker, 1854; 92, Imara satrapes (Kollar, 1839); 93, Telchin evalthe (Fabricius, 1775) comb. nov.; 94, Castnius pelasgus (Cramer, [1779]); 95, Synpalamides hegemon (Kollar, 1839) comb. nov. Scale bars: 1 mm.
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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.