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1,003 results for “darkness”
FIGURES 22–28 in New dark species of the bee genus Colletes (Hymenoptera, Colletidae) from Mexico and Guatemala
FIGURES 22–28. Colletes chiaPensis Balboa & Ayala sp. n. 22—female holotype: habitus, lateral view; 23—female holotype: antennae; 24—female paratype: head; 25—female paratype: propodeum; 26—female paratype: paraocular area and vertex; 27—female holotype: dorsal view of metasoma; 28—female holotype: S6.
FIGURES 1–7 in New dark species of the bee genus Colletes (Hymenoptera, Colletidae) from Mexico and Guatemala
FIGURES 1–7. Colletes tzotzilis Balboa & Ayala sp. n. 1—female holotype: habitus, lateral view; 2—male allotype: habitus, lateral view; 3—female paratype: dorsolateral view of mesosoma; 4—female holotype: dorsal view of mesosoma; 5—male allotype: S7; 6—male allotype: S8; 7—male allotype: genital capsule.
FIGURES 15–21 in New dark species of the bee genus Colletes (Hymenoptera, Colletidae) from Mexico and Guatemala
FIGURES 15–21. Colletes guatemalensis Balboa & Ayala sp. n. 15—female holotype: habitus, lateral view; 16—male allotype: habitus, lateral view; 17—Female paratype: Clypeus; 18—female holotype: dorsal view of metasoma; 19—male allotype: S7; 20—male allotype: S8; 21—male allotype: genital capsule.
FIGURES 8–14 in New dark species of the bee genus Colletes (Hymenoptera, Colletidae) from Mexico and Guatemala
FIGURES 8–14. Colletes jobeli Balboa & Ayala sp. n. 8—female (holotype): habitus, lateral view; 9—male allotype: habitus, lateral view; 10—female holotype: T2 y T3; 11—female paratype: tegula; 12—male allotype: S7; 13—male allotype: S8; 14— male allotype: genital capsule.
FIGURES 43–49 in New dark species of the bee genus Colletes (Hymenoptera, Colletidae) from Mexico and Guatemala
FIGURES 43–49. Colletes isabelae Balboa & Ayala sp. n. 36—female holotype: habitus, lateral view; 44—male allotype: habitus, lateral view; 45—female holotype: detail of clypeus, labrum and mandibles; 46—female holotype: propodeum; 47— male allotype: S7; 48—male allotype: S8; 49—male allotype): genital capsule.
Inlists for "An Alternative Channel to Black Hole Low-Mass X-ray Binaries: Dynamical Friction of Dark Matter? "
<p>In this work, we employ MESA code to diagnose whether the dynamical friction between dark matter and the companion stars can drive BH binaries to evolve toward the observed BH LMXBs and alleviate the effective temperature problem. Assuming that there exists a density spike of dark matter around BH, the dynamical friction can produce an efficient angular momentum loss, driving BH binaries with an intermediate-mass companion star to evolve into BH LMXBs for a spike index higher than $\gamma = 1.58$.</p> <p>MESA version: r12115; SDK compiler: mesasdk-x86_64-linux-20190830</p> <p> </p>
Atomic resolution high-angle annular dark field scanning transmission electron microscopy imaging of WSe2 encapsulated within hexagonal boron nitride
Open the record for dataset details and reuse information.
The natural variance of Arabidopsis secondary metabolism on extended darkness-3
<p>In plants due to their sessile nature, secondary metabolites are important components against different abiotic and biotic stress, such as extended darkness. For this reason, the variation of secondary metabolite content of the Arabidopsis thaliana HapMap natural population following 0- and 6-d darkness treatment were detected and the raw data of different accessions at two timepoints were deposited in the MetaboLights database. Moreover, the annotated secondary metabolites of these samples are presented in this data descriptor, which we believe will be a usefully re-usable resource for future integrative analysis with dark-treated transcripts, proteins or other phenotypic data in order to comprehensively illustrate the multiomic landscape of Arabidopsis in response to the stresses exerted by extended darkness.</p>
The natural variance of Arabidopsis secondary metabolism on extended darkness-6
<p>In plants due to their sessile nature, secondary metabolites are important components against different abiotic and biotic stress, such as extended darkness. For this reason, the variation of secondary metabolite content of the Arabidopsis thaliana HapMap natural population following 0- and 6-d darkness treatment were detected and the raw data of different accessions at two timepoints were deposited in the MetaboLights database. Moreover, the annotated secondary metabolites of these samples are presented in this data descriptor, which we believe will be a usefully re-usable resource for future integrative analysis with dark-treated transcripts, proteins or other phenotypic data in order to comprehensively illustrate the multiomic landscape of Arabidopsis in response to the stresses exerted by extended darkness.</p>
The natural variance of Arabidopsis secondary metabolism on extended darkness-2
<p>In plants due to their sessile nature, secondary metabolites are important components against different abiotic and biotic stress, such as extended darkness. For this reason, the variation of secondary metabolite content of the Arabidopsis thaliana HapMap natural population following 0- and 6-d darkness treatment were detected and the raw data of different accessions at two timepoints were deposited in the MetaboLights database. Moreover, the annotated secondary metabolites of these samples are presented in this data descriptor, which we believe will be a usefully re-usable resource for future integrative analysis with dark-treated transcripts, proteins or other phenotypic data in order to comprehensively illustrate the multiomic landscape of Arabidopsis in response to the stresses exerted by extended darkness.</p>
The natural variance of Arabidopsis secondary metabolism on extended darkness-8
<p>In plants due to their sessile nature, secondary metabolites are important components against different abiotic and biotic stress, such as extended darkness. For this reason, the variation of secondary metabolite content of the Arabidopsis thaliana HapMap natural population following 0- and 6-d darkness treatment were detected and the raw data of different accessions at two timepoints were deposited in the MetaboLights database. Moreover, the annotated secondary metabolites of these samples are presented in this data descriptor, which we believe will be a usefully re-usable resource for future integrative analysis with dark-treated transcripts, proteins or other phenotypic data in order to comprehensively illustrate the multiomic landscape of Arabidopsis in response to the stresses exerted by extended darkness.</p>
The natural variance of Arabidopsis secondary metabolism on extended darkness-10
<p>In plants due to their sessile nature, secondary metabolites are important components against different abiotic and biotic stress, such as extended darkness. For this reason, the variation of secondary metabolite content of the Arabidopsis thaliana HapMap natural population following 0- and 6-d darkness treatment were detected and the raw data of different accessions at two timepoints were deposited in the MetaboLights database. Moreover, the annotated secondary metabolites of these samples are presented in this data descriptor, which we believe will be a usefully re-usable resource for future integrative analysis with dark-treated transcripts, proteins or other phenotypic data in order to comprehensively illustrate the multiomic landscape of Arabidopsis in response to the stresses exerted by extended darkness.</p>
The natural variance of Arabidopsis secondary metabolism on extended darkness-5
<p>In plants due to their sessile nature, secondary metabolites are important components against different abiotic and biotic stress, such as extended darkness. For this reason, the variation of secondary metabolite content of the Arabidopsis thaliana HapMap natural population following 0- and 6-d darkness treatment were detected and the raw data of different accessions at two timepoints were deposited in the MetaboLights database. Moreover, the annotated secondary metabolites of these samples are presented in this data descriptor, which we believe will be a usefully re-usable resource for future integrative analysis with dark-treated transcripts, proteins or other phenotypic data in order to comprehensively illustrate the multiomic landscape of Arabidopsis in response to the stresses exerted by extended darkness.</p>
The natural variance of Arabidopsis secondary metabolism on extended darkness-11
<p>In plants due to their sessile nature, secondary metabolites are important components against different abiotic and biotic stress, such as extended darkness. For this reason, the variation of secondary metabolite content of the Arabidopsis thaliana HapMap natural population following 0- and 6-d darkness treatment were detected and the raw data of different accessions at two timepoints were deposited in the MetaboLights database. Moreover, the annotated secondary metabolites of these samples are presented in this data descriptor, which we believe will be a usefully re-usable resource for future integrative analysis with dark-treated transcripts, proteins or other phenotypic data in order to comprehensively illustrate the multiomic landscape of Arabidopsis in response to the stresses exerted by extended darkness.</p>
The natural variance of Arabidopsis secondary metabolism on extended darkness-12
<p>In plants due to their sessile nature, secondary metabolites are important components against different abiotic and biotic stress, such as extended darkness. For this reason, the variation of secondary metabolite content of the Arabidopsis thaliana HapMap natural population following 0- and 6-d darkness treatment were detected and the raw data of different accessions at two timepoints were deposited in the MetaboLights database. Moreover, the annotated secondary metabolites of these samples are presented in this data descriptor, which we believe will be a usefully re-usable resource for future integrative analysis with dark-treated transcripts, proteins or other phenotypic data in order to comprehensively illustrate the multiomic landscape of Arabidopsis in response to the stresses exerted by extended darkness.</p>
The natural variance of Arabidopsis secondary metabolism on extended darkness-9
<p>In plants due to their sessile nature, secondary metabolites are important components against different abiotic and biotic stress, such as extended darkness. For this reason, the variation of secondary metabolite content of the Arabidopsis thaliana HapMap natural population following 0- and 6-d darkness treatment were detected and the raw data of different accessions at two timepoints were deposited in the MetaboLights database. Moreover, the annotated secondary metabolites of these samples are presented in this data descriptor, which we believe will be a usefully re-usable resource for future integrative analysis with dark-treated transcripts, proteins or other phenotypic data in order to comprehensively illustrate the multiomic landscape of Arabidopsis in response to the stresses exerted by extended darkness.</p>
The natural variance of Arabidopsis secondary metabolism on extended darkness-4
<p>In plants due to their sessile nature, secondary metabolites are important components against different abiotic and biotic stress, such as extended darkness. For this reason, the variation of secondary metabolite content of the Arabidopsis thaliana HapMap natural population following 0- and 6-d darkness treatment were detected and the raw data of different accessions at two timepoints were deposited in the MetaboLights database. Moreover, the annotated secondary metabolites of these samples are presented in this data descriptor, which we believe will be a usefully re-usable resource for future integrative analysis with dark-treated transcripts, proteins or other phenotypic data in order to comprehensively illustrate the multiomic landscape of Arabidopsis in response to the stresses exerted by extended darkness.</p>
The natural variance of Arabidopsis secondary metabolism on extended darkness-7
<p>In plants due to their sessile nature, secondary metabolites are important components against different abiotic and biotic stress, such as extended darkness. For this reason, the variation of secondary metabolite content of the Arabidopsis thaliana HapMap natural population following 0- and 6-d darkness treatment were detected and the raw data of different accessions at two timepoints were deposited in the MetaboLights database. Moreover, the annotated secondary metabolites of these samples are presented in this data descriptor, which we believe will be a usefully re-usable resource for future integrative analysis with dark-treated transcripts, proteins or other phenotypic data in order to comprehensively illustrate the multiomic landscape of Arabidopsis in response to the stresses exerted by extended darkness.</p>
The natural variance of Arabidopsis secondary metabolism on extended darkness-13
<p>In plants due to their sessile nature, secondary metabolites are important components against different abiotic and biotic stress, such as extended darkness. For this reason, the variation of secondary metabolite content of the Arabidopsis thaliana HapMap natural population following 0- and 6-d darkness treatment were detected and the raw data of different accessions at two timepoints were deposited in the MetaboLights database. Moreover, the annotated secondary metabolites of these samples are presented in this data descriptor, which we believe will be a usefully re-usable resource for future integrative analysis with dark-treated transcripts, proteins or other phenotypic data in order to comprehensively illustrate the multiomic landscape of Arabidopsis in response to the stresses exerted by extended darkness.</p>
The natural variance of Arabidopsis secondary metabolism on extended darkness-1
<p>In plants due to their sessile nature, secondary metabolites are important components against different abiotic and biotic stress, such as extended darkness. For this reason, the variation of secondary metabolite content of the Arabidopsis thaliana HapMap natural population following 0- and 6-d darkness treatment were detected and the raw data of different accessions at two timepoints were deposited in the MetaboLights database. Moreover, the annotated secondary metabolites of these samples are presented in this data descriptor, which we believe will be a usefully re-usable resource for future integrative analysis with dark-treated transcripts, proteins or other phenotypic data in order to comprehensively illustrate the multiomic landscape of Arabidopsis in response to the stresses exerted by extended darkness.</p>
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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)
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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.