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62 results for “plant accumulation”
Supplementary material 3 from: Egawa C, Koyama A (2023) Temporal trends in the accumulation of alien vascular plant species through intentional and unintentional introductions in Japan. NeoBiota 83: 179-196. https://doi.org/10.3897/neobiota.83.101416
Generalised additive model (GAM) results
Fig. 3. Key NOESY correlations observed for compounds 1 and 2 in Isoavenaciol and 7-hydroxy-isoavenaciol: Zn-chelating metallophores produced by root-endophytic Pezicula ericae in a Zn-accumulating plant, Aucuba japonica
Fig. 3. Key NOESY correlations observed for compounds 1 and 2.
Fig. 5 in Isoavenaciol and 7-hydroxy-isoavenaciol: Zn-chelating metallophores produced by root-endophytic Pezicula ericae in a Zn-accumulating plant, Aucuba japonica
Fig. 5. Partial structure of isoavenaciol hydrolysate in CD3OD.
Fig. 2. Key HMBC correlations observed for compound 1 in Isoavenaciol and 7-hydroxy-isoavenaciol: Zn-chelating metallophores produced by root-endophytic Pezicula ericae in a Zn-accumulating plant, Aucuba japonica
Fig. 2. Key HMBC correlations observed for compound 1.
Fig. 1 in Sites of biosynthesis and storage of Taxol in Taxus media (Rehder) plants: Mechanism of accumulation
Fig. 1. Summarized Taxol biosynthetic pathway.
Data from: Alteration of nitrous oxide emissions from floodplain soils by aggregate size, litter accumulation and plant–soil interactions
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Data from: Effect of cadmium accumulation on the performance of plants and of herbivores that cope differently with organic defenses
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Data from: Ambient nitrogen deposition drives plant-diversity decline by nitrogen accumulation in a closed grassland ecosystem
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Accumulation of TuMV-derived siRNAs in aerial parts of Arabidopsis thaliana plants at 7 and 10 dpi
GEO Series GSE20197. Arabidopsis thaliana; Turnip mosaic virus. 36 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Transcriptomic comparison between nickel hyperaccumulator and non-accumulator plant species from diverse genera and geographic locations
GEO Series GSE116054. Leucocroton havanensis; Geissois pruinosa; [Phyllanthus] conjugatus var. ducosensis; Noccaea caerulescens; Geissois racemosa; Psychotria revoluta; Homalium betulifolium; Psychotria semperflorens; Thlaspi montanum; Psychotria grandis; Lasiocroton microphyllus; Psychotria costivenia; Psychotria gabriellae; Homalium kanaliense; Phyllanthus luciliae. 43 samples. Type: Expression profiling by high throughput sequencing.
Transcriptomic comparison between nickel hyperaccumulator and non-accumulator plant species from the Leucocroton and Lasiocroton genus (Euphorbiaceae) from Cuba
GEO Series GSE116049. Lasiocroton microphyllus; Leucocroton havanensis. 3 samples. Type: Expression profiling by high throughput sequencing.
Transcriptomic comparison between nickel hyperaccumulator and non-accumulator plant species from the Phyllanthus genus (Phyllanthaceae) from New Caledonia.
GEO Series GSE154372. [Phyllanthus] conjugatus var. ducosensis; Phyllanthus luciliae. 6 samples. Type: Expression profiling by high throughput sequencing.
Transcriptomic comparison between nickel hyperaccumulator and non-accumulator plant species from the Noccaea genus (Brassicaceae) from France
GEO Series GSE115411. Thlaspi montanum; Noccaea caerulescens. 10 samples. Type: Expression profiling by high throughput sequencing.
Transcriptomic comparison between nickel hyperaccumulator and non-accumulator plant species from the Psychotria genus (Rubiacaeae) from Cuba
GEO Series GSE116050. Psychotria revoluta; Psychotria grandis; Psychotria costivenia. 6 samples. Type: Expression profiling by high throughput sequencing.
Transcriptomic comparison between nickel hyperaccumulator and non-accumulator plant species from the Geissois genus (Cunoniaceae) endemic from New Caledonia
GEO Series GSE116048. Geissois racemosa; Geissois pruinosa. 6 samples. Type: Expression profiling by high throughput sequencing.
Data from: Soil carbon accumulation differences: allocation of visible plant biomass, carbon and nitrogen in two turfgrasses
<p><span>Carbon accumulation in turfgrass soils by plant material may be beneficial to CO<sub>2</sub> sequestration and soil health, but at high rates can easily lead to declined turfgrass quality (i.e. thatch and mat layer formation). In a field study it was investigated how the fraction of visible plant biomass of turfgrass (sub)species monocultures, with two or three varieties as monoculture per (sub)species, and its C and N concentration and CN ratio in this visible plant biomass in thatch, mat and soil layers contributes to C accumulation. In total three <em>Festuca rubra</em> subspecies; <em>Festcua rubra commutata</em> (Frc), <em>Festuca rubra trichophylla </em>(Frt), <em>Festuca rubra rubra</em> (Frr), and three Agrostis species; <em>Agrostis canina</em> (Acn), <em>Agrostis capillaris</em> (Acp), Agrostis stolonifera (As), were studied. The study was conducted on 3 years old turfgrass demonstration fields of two turfgrass seed companies: <em>Festuca rubra</em> subspecies samples were collected at a site of Barenbrug in Wolfheze (52°00´N, 5°46´E), and <em>Agrostis </em>species were sampled at a site of DLF in Moerstraten (51°32´N, 4°20´E), both in the Netherlands. Both sites were built on a sandy soil. </span></p> <p><span>For every variety, cores of the top 20 cm of the soil including aboveground biomass were taken with a core sampler (diameter 28 mm). The core was immediately divided into 4 distinctive layers, thatch + aboveground biomass, mat, remaining upper 10 cm soil and 10-20 cm soil. Distinction of these layers followed the protocol of Evers et al. (2024). </span><span>Aboveground biomass was separated from the thatch with scissors. Sediment from thatch, mat, remaining upper 10 cm of soil and 10-20 cm soil was carefully washed out with tap water, after which the remaining below-ground (dead and living) visible plant biomass and aboveground biomass was dried at 65 °C until stable weight and weighed. Total C and N analyses were carried out with a Vario Micro Cube Element Analyzer (Elementar, Langenselbold, Germany), from which C and N concentrations (in % of dry matter of plant biomass) and C to N ratios (CN ratio) were calculated.</span></p>
Transcriptomic comparison between nickel hyperaccumulator and non-accumulator plant species from the Homalium genus (Salicaceae) endemic from New Caledonia
GEO Series GSE116052. Homalium kanaliense; Homalium betulifolium. 6 samples. Type: Expression profiling by high throughput sequencing.
Transcriptomic comparison between nickel hyperaccumulator and non-accumulator plant species from the Psychotria genus (Rubiacaeae) endemic from New Caledonia
GEO Series GSE116051. Psychotria gabriellae; Psychotria semperflorens. 6 samples. Type: Expression profiling by high throughput sequencing.
Zinc accumulation in Atriplex lentiformis is driven by plant genes and the soil microbiome
GEO Series GSE208352. Atriplex lentiformis. 9 samples. Type: Expression profiling by high throughput sequencing.
Overexpression of ENOD40 in Arabidopsis thaliana plants reveals a role of the gene in cell wall turnover and glucosinolate accumulation.
GEO Series GSE37867. Arabidopsis thaliana. 12 samples. Type: Expression profiling by array.
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International Brain Laboratory public data
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OpenNeuro
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