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769 results for “CULTIVATE”
Data from: Population structure of Venturia inaequalis, a causal agent of apple scab, in response to heterogeneous apple tree cultivation
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Data from: Phenotypic landscapes: phenological patterns in wild and cultivated barley
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Data from: Species composition and community structure of small pest rodents (Muridae) in cultivated and fallow fields in maize growing areas in Mayuge district, Eastern Uganda
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Cultivating scientific literacy and a sense of place through course-based urban ecology research
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Data from: Metabolism and the rise of fungus cultivation by ants
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Testing sunfish as zooplankton control agents for wastewater-algal cultivation: Nutrient, invertebrate, and algae data
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Data from: Rapid evolution in native plants cultivated for ecological restoration: not a general pattern
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Effects of cultivation practice on floristic and flowering diversity of spontaneously growing plant species on arable fields
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Data from: Independent domestications of cultivated tree peonies from different wild peony species
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Population structure of Rosa spinosissima L. on the Frisian Islands and introgression from cultivated material
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Can sensors help in reducing costs associated with cultivated meat production?
<p>Cell culture medium is the most significant cost driver for cultivated meat production. Optimizing bioreactors’ design and instrumentation, through additional monitoring features via sensors can help in decreasing these costs, and achieving maximum cell production capacity per unit medium volume. <br> In Realsense1 (RS1) project, we focus on developing and testing novel low-cost sensors in the lab-on-a-chip environment i.e. microfluidic bioreactors, which enable significant reduction in time and cost of bioprocessing development due to the high degree of control over process variables through controlled fluid behavior characterized by the laminar flow, diffusion mixing and rapid energy dissipation. <br> In the follow-up Realsense 2 project, we use mathematical modeling and computational fluid dynamics coupled to empirical data generated in RS1 to identify the most efficient configuration for integrating sensors into stirred-tank bioreactors.</p> <p>This webinar discusses both projects, presents current results on microbioreactor design and fabrication and specific developed sensors, as well as the next steps for further scale-up options.</p>
Figure 6 from: Popova P, Zarev Y, Shkondrov A, Krasteva I, Ionkova I (2020) Induction of flavonoid biosynthesis by in vitro cultivation of Astragalus glycyphyllos L. Pharmacia 67(2): 95-99. https://doi.org/10.3897/pharmacia.67.e50390
Figure 6 Total flavonoid contents (mg/mg DW) in suspension cultures of A. glycyphyllos, cultivated on G48 medium, supplemented with 10, 20 and 30 mg/mL quercetin.
Figure 3 from: Popova P, Zarev Y, Shkondrov A, Krasteva I, Ionkova I (2020) Induction of flavonoid biosynthesis by in vitro cultivation of Astragalus glycyphyllos L. Pharmacia 67(2): 95-99. https://doi.org/10.3897/pharmacia.67.e50390
Figure 3 Growth index of callus cultures of A. glycyphyllos, cultivated on culture mediums with half and double amount of Mg2+ and Ca2+.
Figure 5 from: Popova P, Zarev Y, Shkondrov A, Krasteva I, Ionkova I (2020) Induction of flavonoid biosynthesis by in vitro cultivation of Astragalus glycyphyllos L. Pharmacia 67(2): 95-99. https://doi.org/10.3897/pharmacia.67.e50390
Figure 5 Total flavonoid contents (mg/g DW) of callus cultures of A. glycyphyllos, cultivated on culture mediums with half and double amount of Mg2+ and Ca2+ under light regimen of cultivation.
Is drought tolerance a domestication trait in tepary bean?: Allelic diversity at abiotic stress responsive genes in cultivated Phaseolus acutifolius A. Gray and its wild relatives
<p>Some of the major impacts of climate change are expected in the poorest regions of the world where drought stress and nutrient deficiency are already a main issue. Legumes are an essential food crop for the poorest because of their high dietary protein and micronutrient contents. However, they are generally drought susceptible. Therefore, our goal in this study was to explore allele diversity at abiotic stress responsive candidate genes in the only drought tolerant cultivated bean species of the genus <i>Phaseolus</i>, tepary bean (<i>P. acutifolius</i> A. Gray) and its related species <i>P. parvifolius </i>Freytag. Specifically, we estimated drought tolerance in 52 tepary bean <i>s.l.</i> geo-referenced germplasm accessions from the <i>P. acutifolius</i>–<i>parvifolius</i> clade using climate information, and used this estimated drought stress index to examine allele correlations with <i>Asr2</i>, <i>Dreb2B</i> and ERECTA-encoding candidate genes for drought tolerance. Genetic clustering showed that cultivated and wild <i>P. acutifolius</i> were intermingled with <i>P. acutifolius </i>var.<i> tenuifolius</i> and <i>P. parvifolius</i>, signifying that allele diversity at candidate genes for drought tolerance was not scarce in tepary bean <i>s.l</i>. <i>Dreb2B</i> and ERECTA-encoding genes harbored signatures of directional/purifying selection, likely in favor of adaptive alleles selectively advantageous because each had two SNPs significantly correlated (<i>p-value</i> < 0.05) with habitat drought stress at six and 12 months. These results suggest that tepary bean <i>s.l. </i>is a reservoir of novel alleles at candidate genes for drought tolerance, as expected for a drought-tolerant species that originated in warmer and arid environments. Abiotic stress responsive candidate genes also exhibit comparable patterns of selective signatures when comparing orthologous across species, which speaks for a predominant role of gene sub-functionalization likely due to ecological constrains. Our study therefore corroborates that the candidate gene approach is still an effective alternative for marker validation across a broader genetic basis of germplasm accessions. Further efforts to determine the genetic architecture of drought tolerance will unlock novel alleles hidden in a crop with limited modern relevance as tepary bean, but capable of acting as a donor in backcrossing and genome editing strategies with elite common bean lines aiming to meet the imminent demands of a drier world.</p>
Figure 8 in New eriophyoid mites (Acari: Prostigmata: Eriophyoidea) from cultivated plants from northeastern Brazil, including the second taxon in the Prothricinae
Figure 8. Tegolophus indica. (A) Dorsal habitus, female; (B) ventral habitus, female; (C) epigynum; (D) genitalia, male; (E) detail of prodorsal shield; (F) leg I and leg II, female; (G) empodium.
Figure 5 in New eriophyoid mites (Acari: Prostigmata: Eriophyoidea) from cultivated plants from northeastern Brazil, including the second taxon in the Prothricinae
Figure 5. Thamnacus paubrasil sp. nov. CGM, coxigenital region, male; D, dorsal habitus, female; em, empodium, leg I, female; LM, lateral habitus, female; L1, leg I, female; L2, leg II, female; V, ventral habitus, female.
Figure 4 in New eriophyoid mites (Acari: Prostigmata: Eriophyoidea) from cultivated plants from northeastern Brazil, including the second taxon in the Prothricinae
Figure 4. Auriculatus clitoria gen. nov., sp. nov. (A) Dorsal habitus, female; (B) ventral habitus, female; (C) lateral habitus, female; (D) leg I and II, female; (E) epigynum; (F) genitalia, male; (G) empodium, female.
Figure 3 in New eriophyoid mites (Acari: Prostigmata: Eriophyoidea) from cultivated plants from northeastern Brazil, including the second taxon in the Prothricinae
Figure 3. Auriculatus clitoria gen. nov., sp. nov. CGM, coxigenital region, male; D, dorsal habitus, female; em, empodium, leg I, female; LM, lateral habitus, female; L1, leg I, female; L2, leg II, female; V, ventral habitus, female.
Figure 2 in New eriophyoid mites (Acari: Prostigmata: Eriophyoidea) from cultivated plants from northeastern Brazil, including the second taxon in the Prothricinae
Figure 2. Neoprothrix hibiscus gen. nov., sp. nov. (A) Dorsal habitus, female; (B) ventral habitus, female; (C) epigynum; (D) genitalia, male; (E) dorsal seta; (F) dorsal seta amplified; (G) internal seta; (H) leg I, female; (I). leg II, female.
ScienceDex guides
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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.