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105 results for “acid growth”
Ascorbic Acid Hydrolysate of Kappaphycus alvarezii as an Effective Biostimulant for Growth and Crop Yield Improvement of Hybrid Maize in Vietnam
<p>The study<strong> </strong>researches on plant production with particular attention to the environment. It first mentions the usage of ascorbic acid for depolymerization of carrageenans from dry <em>K. alvarezii</em> biomass, its hydrolysate’ characteristics, and its positive influence on the hybrid maize crop in Vietnam. The study is one of the very fewer studies evaluating the plant-growth promoting activity of oligocarrageenans on maize crops. The results of the study introduce an oligocarrageenans-rich biostimulant prepared by acid hydrolysis of <em>K. alvarezii </em>seaweed in ascorbic acid, and positive impacts of foliar spraying of the hydrolysate (at different Mw of oligocarrageenans and concentrations) on the hybrid maize crop in Vietnam. The application of this product resulted in increases in efficiency of nutrient uptake by the plant, plant height (~20. 6%), and grain yield (by 21.3% over the control). Therefore, it is suitable for application on a large scale agriculture to reduce the chemical fertilizers used</p>
Figure 1 in Ontogenetic changes in nucleic acid, protein contents, and growth of larval and juvenile Japanese flounder
Figure 1. Body mass (◆) and total length (■) of Japanese flounder during larval and juvenile development related to days after hatching. Values are given as the mean ± SD. Each value is obtained from 35 individuals.
Figure 2 in Ontogenetic changes in nucleic acid, protein contents, and growth of larval and juvenile Japanese flounder
Figure 2. Instantaneous growth rate (A) and absolute growth rate (B) of body mass (◆) and total length (v) in Japanese flounder during larval and juvenile development related to days after hatching. Values are given as the mean ± SD. Each value is obtained from 35 individuals.
Figure 4 in Ontogenetic changes in nucleic acid, protein contents, and growth of larval and juvenile Japanese flounder
Figure 4. Changes in DNA content (■) and DNA concentration (◆) of Japanese flounder larvae and juveniles. Values are given as the mean ± SD. The numbers of samples collected each day range from 5 pools of 560 fish initially to 10 individual fish.
Figure 7 in Ontogenetic changes in nucleic acid, protein contents, and growth of larval and juvenile Japanese flounder
Figure 7. Diel variation of the RNA/DNA ratio in the fed () and starved (■) Japanese flounder larvae during the 48-h period. Values are given as the mean ± SD. Each value is obtained from 15 individuals. The dark line means the dark time.
Figure 3 in Ontogenetic changes in nucleic acid, protein contents, and growth of larval and juvenile Japanese flounder
Figure 3. Changes in protein content (■) and protein concentration (◆) of Japanese flounder larvae and juveniles. Values are given as the mean ± SD. The numbers of samples collected each day range from 5 pools of 560 fish initially to 10 individual fish.
Figure 6 in Ontogenetic changes in nucleic acid, protein contents, and growth of larval and juvenile Japanese flounder
Figure 6. Changes in protein/DNA (■) and RNA/DNA (◆) of Japanese flounder larvae and juveniles. Values are given as the mean ± SD. The numbers of samples collected each day range from 5 pools of 560 fish initially to 10 individual fish.
Figure 5 in Ontogenetic changes in nucleic acid, protein contents, and growth of larval and juvenile Japanese flounder
Figure 5. Changes in RNA content (■) and RNA concentration (◆) of Japanese flounder larvae and juveniles. Values are given as the mean ± SD. The numbers of samples collected each day range from 5 pools of 560 fish initially to 10 individual fish.
Figure 8 in Ontogenetic changes in nucleic acid, protein contents, and growth of larval and juvenile Japanese flounder
Figure 8. Changes in RNA/DNA ratios of Japanese flounder exposed to different starved-refeeding treatments from 20 to 27 days after hatching: (A) fed (control treatment), (B) 1-day starved, (C) 2-day starved, (D) 3-day starved, (E) 4-day starved. Values are given as the mean ± SD. Each value is obtained from 10 individuals. Dark symbols mean feeding days and empty symbols mean starved days.
Defining fatty acids changes linked to rumen development, weaning and growth within Holstein-Friesian heifers
<p>After birth, as effectively monogastric animals, calves undergo substantial physiological changes to become ruminants by 3 months of age and reach sexual maturity at approximately 15 months of age. Herein, we assess longitudinal metabolomic changes in Holstein-Friesian (HF) heifers from birth until sexual maturity during this developmental process. Sera from 20 healthy, HF heifers were sampled biweekly from 2 weeks of age until 13 months of age and then monthly until 19 months of age. Sera were assessed using flow infusion electrospray high resolution mass spectrometry (FIE-HRMS) on a Q Exactive hybrid quadrupole-Orbitrap mass spectrometer for high throughput, sensitive, non-targeted metabolite fingerprinting. Partial least squares-discriminate analysis (PLS-DA) and unsupervised hierarchical clustering analysis (HCA) of the derived metabolomes indicated changes detectable in heifers’ sera over time. Time series analyses identified 30 metabolites that could be related to rumen development and weaning at ~ 3 months of age. Further time series analysis identified 40 metabolites that could be correlated to growth. These findings highlight the role of acetic acid and 3-PP within rumen development and growth, suggest that weaning induces elevated levels of fatty acyls in response to a post-weaning stress induced innate immune response and demonstrate the utilisation of fatty acyls in growth. The identified metabolites offer serum metabolites which could inform the nutrition and healthy development of heifers</p>
Growth data was collected on one deciduous shrub species on Arctic LTER experimental plots in moist acidic tussock and dry heath tundra 2004, Toolik Field Station, Alaska.
Weekly growth of plant species of three growth forms were measured in the ninth year of a long-term experiment at Toolik Field Station. The experimental treatments excluded small and large mammalian herbivores and increased soil nutrients in two arctic Alaskan tundra communities: moist acidic tussock and dry heath. This data set reports the deciduous dwarf shrub species. Please see 2004lggrgram for the tussock-forming and rhizomatous graminoid species growth data.
Growth data was collected on four graminoid species on Arctic LTER experimental plots in moist acidic tussock and dry heath tundra 2004, Toolik Field Station, Alaska.
Weekly growth of plant species of three growth forms were measured in the ninth year of a long-term experiment at Toolik Field Station. The experimental treatments excluded small and large mammalian herbivores and increased soil nutrients in two arctic Alaskan tundra communities: moist acidic tussock and dry heath. This data set reports the four graminoid (both tussock and rhizomatous forms) species. Please see 2004lggrbnan for Betula nana (dwarf shrub) growth data.
Black solider fly survival, growth, pupation and fatty acid composition
<p>data on BSFL survival, growth, pupation and fatty acid composition</p>
Metadata of " Synthesis of (poly)gallic acid in a bacterial growth medium"
<p>Metadata of " Synthesis of (poly)gallic acid in a bacterial growth medium"</p>
Safety, Tolerability, Efficacy, Pharmacokinetics, and Pharmacodynamics of Sebelipase Alfa in Children With Growth Failure Due to Lysosomal Acid Lipase Deficiency
ClinicalTrials.gov study NCT01371825. IPD Sharing: UNDECIDED. Countries: 5. Publications: 1.
Pertuzumab in Platinum-Resistant Low Human Epidermal Growth Factor Receptor 3 (HER3) Messenger Ribonucleic Acid (mRNA) Epithelial Ovarian Cancer (PENELOPE)
ClinicalTrials.gov study NCT01684878. IPD Sharing: Not stated. Countries: 10. Publications: 1.
Free Fatty Acids, Body Weight, and Growth Hormones Secretion in Children
ClinicalTrials.gov study NCT01237041. IPD Sharing: Not stated. Countries: 1. Publications: 4.
Growth and Adiposity in Newborns: The Influence of Prenatal Docosahexaenoic Acid (DHA) Supplementation
ClinicalTrials.gov study NCT03310983. IPD Sharing: Not stated. Countries: 1. Publications: 2.
Data on weights and lengths from retrospective growth analysis of different stem age classes of Betula nana ramets from the Arctic LTER Nutrient and Warming manipulations in mosit acidic tussock tundra at 1995, Toolik Lake, AK.
This data file contains the data on weights and lengths from retrospective growth analysis of different stem age classes of Betula nana ramets from the Arctic LTER Nutrient and Warming manipulations in moist acidic tussock tundra at Toolik Lake.
Rapid growth of new atmospheric particles by nitric acid and ammonia condensation: data resources
<p>Data presented in the manuscript "Rapid growth of new atmospheric particles by nitric acid and ammonia condensation" currently in review.</p> <p> </p> <p>The manuscript associated with this data was written using results from the CLOUD experiment at CERN, and the author list is a subset of the CLOUD collaboration.</p> <p> </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)
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.