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nutrient acquisition

9498 relationships annotated with this phrase. Showing first 500 of 9498.
Source entity Relationship Target entity Species
nutrient supplementation indicates that floral traits should be at least as responsive to arbuscular mycorrhizal fungi (AMF)
consumption of the vacuole would allow for parasite to immediately consume the major polysaccharide storage within the host cell Maullinia ectocarpii
fungi is key to enhancing plant nutrient-acquisition strategies
root hairs have a role in absorbing nutrients
efficient nutrient uptake by plants would allow for coupling of plant and ant colony growth Caularthron bilamellatum
vascular epiphyte morphological adaptations enable nutrient uptake from decomposing organic matter from plants, insects, birds or other organisms
plants secret exudates to recruit microbiomes in exchange for nutrients
root morphology plays central role in acquisition of soil P
close interface between the parasite and the amyloplast allows consumption of leaked sugars without cutting the organelle off from the nucleus Plasmodiophora brassicae
species with higher root morphological and anatomical plasticity may show greater P-uptake rate when P limitation is alleviated
species with larger genomes have higher nitrogen (N) demands
thick melanized hyphae and thin endophytic hyphae results in synergism in nutrient uptake Caularthron bilamellatum
Representation of nitrogen (N) acquisition processes was more developed than phosphorus (P) acquisition
association with ants enables access to nutrient resources
ant presence enhances nutrient uptake capabilities Caularthron bilamellatum
plants at vigorous vegetative and reproductive developmental stages have requirement for large amount of nutrients
antifungal nature of Bg_9562 enables bacterium to utilize plant-associated fungi as nutrient source Burkholderia gladioli
fine roots are involved in nutrient acquisition
Caularthron bilamellatum sacrifices water storage tissue Caularthron bilamellatum
AM fungi and phosphate-solubilizing bacteria (PSB) significantly increased plant phosphorus (P) content
new root hair mutants in grasses have the potential to illuminate mechanisms of plant nutrition
mycorrhizal fungi enhance plant's ability to acquire nutrients (especially N and P) critical to floral display
enhanced nutrient availability in soil and pathogen suppression promote nutrient uptake
endophytic fungi may be functionally equivalent to mycorrhizal mycelia in roots
intracellular eukaryotic parasites can obtain macromolecules from their host via endocytosis
C3 and C4 grasses show correlation between root PUR and Pn in response to soil P availability
hyphosphere microbiome play important roles on nutrient acquisition for the mycorrhizal pathway
advanced genotypes have greater greater total nutrient content per length compared with reduced genotypes
plants receive approximately 50% of their nitrogen from associations with AMF
drought stress strongly limits nutrient uptake
ant wastes contribute to nutrient needs of host plant
combination of root morphology and anatomy can more comprehensively enhance soil volume from which roots can acquire P and water
RSL overexpression did not improve phosphate uptake and content
enhanced growth of both plants and fungi may increase need and capacity for symbiotic nutrient provision
hydrogen sulphide at 15 micromolar concentration caused reduction of 80% in phosphorous uptake rice cultivars
higher root contact with soil increases ability to take up nutrients Cleistogenes squarrosa
changes in leaf [Mn] were positively correlated with leaf [P]
ECM species in mixed cultures demonstrate preference for carbon over nitrogen
ant waste in hollow pseudobulbs serves as nutrient source Caularthron bilamellatum
N addition may directly alleviate N limitation for plants
plant growth is limited by phosphorus (P)
specific rhizosphere metabolites enriched by intercropping may enhance nutrient uptake Zea mays
AM woody plants exhibit higher foliar N and P concentrations
access to nutrients may be more important than water storage Caularthron bilamellatum
importance of nutrient supply from ants to plants may be different depending on ecology and habitat of the host plant
Plasmodiophora brassicae glucose transporters have been found to significantly increase in late stages of infection Plasmodiophora brassicae
low soluble phosphorus (P) concentration in soils may stimulate plants and microorganisms to secrete more phosphatase
AM fungi increase plant uptake of other elements
root system responsiveness enables exploitation of high nutrient density regions
buzz mutant has no statistically significant difference in total nitrogen in shoots and roots compared with Bd21 Brachypodium distachyon
Restionaceae has evolved cluster roots
Caularthron bilamellatum is epiphytic orchid Caularthron bilamellatum
arbuscular mycorrhizal (AM), ectomycorrhizal (ECM), or ericoid mycorrhizal (ERM) fungi enable access to soil nutrients
enhanced nutrient availability in rhizosphere facilitate greater plant nutrient uptake
plants at high-altitude biome exhibit conservative resource-use strategy to adapt to nutrient limitation at high-altitude biome woody plant species
establishing arbuscular mycorrhizal fungal (AMF) symbioses is outsource P-acquisition strategy
study by Gegenbauer et al. informs understanding of diversity of strategies used by plants to acquire nutrients
positive feedbacks involve mycorrhizal symbioses
The most common nutrient parameter functionally related to nutrient uptake in the models was rate of nitrogen (N) uptake, which was responsive to changes in soil nutrient availability (five models), followed by the rate of phosphorus (P) uptake (four models)
EcM woody plants have lower foliar N and P concentrations
mycorrhizal symbioses are important for P capture
extraradical hyphae of AM fungi improve plant phosphorus (P) nutrition
P found predominantly in topsoil suggests that increasing distribution of roots in topsoil may increase P-acquisition
plants should increase biomass allocation to roots
reduced transpiration (E) can restrict nutrient uptake
phosphorus (P) relations is a leading explanation for why plants engage in arbuscular mycorrhizal fungi (AMF) symbiosis
pesticides may be responsible for reduced arbuscular mycorrhizal fungi (AMF)-mediated nutrient acquisition from agricultural soils
angiosperms compared to gymnosperms, have higher leaf nitrogen content
delayed transition into the role of axial transport may allow roots to acquire more resources from the surrounding soil for a greater length of time
root length and root density are positively correlated with mineral element uptake
axial roots have particular importance in P acquisition
transgenic tobacco plants with an enhanced root system showed better growth on medium with low Mg content Nicotiana tabacum
root elongation can improve subsoil foraging for mobile resources Zea mays
transgenic barley plants with enhanced root system show increased accumulation of several soil nutrients in leaves and seeds Hordeum vulgare
greater rooting depth results in greater capture of deep soil resources by remaining axial roots Zea mays
altered CK status of the root may improve acquisition of soil nutrients
crown roots are responsible primarily for soil resource acquisition Zea mays
patterning and characteristics of root hairs leads to increased absorptive surface of the root Arabidopsis thaliana
poor root growth causes reduced efficiency of water and nutrient uptake
maize lines with small crown root number (CN) had greater nitrogen (N) acquisition from deep soil strata Zea mays
better P acquisition occurs under suboptimal P availability Zea mays
empirical observations of plants grown in controlled environment mesocosms and in the field are utilized to explore effect of reduced secondary growth of roots on phosphorus (P) acquisition
production of axial roots is particularly important for balance between capture of mobile and immobile resources
axial roots of monocot crops have fewer mycorrhizal symbioses than dicot crops
increased root distribution in surface soil strata may be disadvantageous for capture of mobile soil resources like water and N Zea mays
increased total volume of soil explored increases acquisition of soil resources
specific root length is root morphological adaptation to P stress
increased root distribution in surface soil strata could facilitate topsoil foraging for immobile resources like P Zea mays
Phosphorus (P) has suboptimal availability for plant growth
shallow root growth angles enables increased topsoil foraging
contrasting architectural strategies have important implications for spatiotemporal dynamics of topsoil foraging
roots under phosphorus (P) stress achieve greater exploration of soil domains that have not been depleted of phosphorus (P)
soil resource acquisition is especially important for P Zea mays
interplant competition is quite small for P acquisition
phosphorus (P) availability is primary limitation to plant growth
AM fungi improve mineral nutrition (particularly phosphate) of the partner
common bean (Phaseolus vulgaris) with greater basal root whorl number had shallower rooting and greater root length topsoil foraging Phaseolus vulgaris
root cortical aerenchyma is beneficial for capture of the immobile resources P and K Zea mays
nutrient-starved conditions allow plants to modify roots to efficiently explore heterogeneous soil environment for nutrients
Yellow Stripe-Like (YSL) proteins are involved in soil scavenging
increasing CK degradation in roots by root-specific expression of a CKX gene causes increased accumulation of micronutrients and macronutrients in aerial plant parts
axial roots of monocot crops have fewer mycorrhizal symbioses
efficient nutrient uptake by plants would be beneficial for both plant and ant mutualistic partners Caularthron bilamellatum
iron sulphide plaques hamper nutrient uptake wild rice
filamentous cyanobacterium found in biocrusts secret exudates to recruit microbiomes in exchange for nutrients
New data presented here from Panama and Singapore demonstrate variation in nutrient uptake rates for different nutrients, with some links to root morphological traits that could be used to further develop resource acquisition syndromes
ectomycorrhizal (ECM) fungi are capable of using organic forms of nutrients
root system is important for nutrient uptake
reduced root secondary growth improves phosphorus capture Phaseolus vulgaris
development of root length can improve soil resource acquisition Zea mays
soil pH has strong impact on availability of mineral nutrients
plant roots explore soil
pollen grains must retrieve all of their nutrients from locular fluid
ammonium uptake results in root acidification Oryza sativa
mutualistic biotrophic fungi differ in nutritional strategies
mycorrhizas affect aphid fitness through improved nutrition
studies in progress examine responses of different crops and cultivars to immobile resources (e.g. phosphate and iron)
biotrophic pathogens are equipped to utilize nutrients provided by living plant cells
beneficial bacteria use ACC as nitrogen source
mineral nutrients are primarily acquired from soil
lateral roots is important for phosphorus acquisition Zea mays
root hairs provide access to immobile nutrients such as phosphate (Pi) Arabidopsis thaliana
plant roots acquire nutrients from soil
plants are dependent on nutrient ion uptake from the soil
nitrogen is essential macronutrient
symbiotic associations improve plant nutrition
structurally related proteins can mediate uptake from the soil
low-molecular-weight organic acid (OA) extrusion is critical for plant nutrition
epidermal and cortical cells receive sufficient O2 for ion transport Triticum aestivum
rice root volume may also enhance absorption of other nutrients Oryza sativa
feeding site functions for nutrient uptake
plants have developed sophisticated mechanisms to improve the acquisition of immobile nutrients
certain fungi provide nutrients
larger root volume increases root surface area
Arbuscular mycorrhiza (AM) improves uptake of phosphorus (P)
root system architecture (RSA) defines macronutrient uptake efficiency
fungal symbionts deliver inorganic phosphate (Pi)
Arbuscular mycorrhiza (AM) improves uptake of water and mineral nutrients
transpirational water flux may be beneficial in aiding nutrient uptake
upregulation of plant SWEET genes promotes bacterial growth due to increased carbon availability
bacterial enzymes aid dissolution of periphyton into vital nutrients in enclosed bladder environment Utricularia
Utricularia and Genlisea are prime candidates for further research on novel plant nitrogen/nutrient utilization pathways Utricularia; Genlisea
Nepenthes ampullaria pitchers possess suite of morphological adaptations Nepenthes ampullaria
phosphorus (P) uptake is dependent on root
decreased nitrate uptake by Pi starvation suggests interdependence of N and P acquisition
disruption of proteostasis by hemi-biotrophic or necrotrophic pathogens allows pathogens to extract nutrients, including essential amino acids
expression of nitrate transporters was elevated in spring Picea abies
plant performance depends directly on Phosphate (Pi) nutrition
Strategy II plants include graminaceous monocot barley Hordeum vulgare L.
low Pi triggers increase of Pi uptake capacity
Somma et al. (1998) model did not directly relate to nutrient uptake
ethylene production increases under phosphorus deficiency
ethylene is involved in regulation of promotion of root hairs
stylet acts as syringe for nutrient uptake from giant cell cytoplasm
Nepenthes pitcher plant species differ in pitcher longevity Nepenthes ampullaria; Nepenthes bicalcarata; Nepenthes rafflesiana
plant uptake of Fe involves complex processes
two transport steps, one in the epidermis and cortex to accumulate ions from the solution and another in the stele to load ions into the xylem is important for understanding inhibitory effects of root zone hypoxia on nutrient acquisition Triticum aestivum
mathematical models have been used to estimate spatial extent of nutrient depletion around rhizosphere
Nepenthes pitcher plant species differ in prey capture rates Nepenthes ampullaria; Nepenthes bicalcarata; Nepenthes rafflesiana
microstructure of inner pitcher wall could be related to nutrient sequestration strategy Nepenthes
superior tolerance to high soil temperatures of thermal Agrostis scabra is manifested by nitrate uptake Agrostis scabra
organic nitrogen (oN) is potentially important soil-derived N source for plants
12C/13C and 14N/15N isotope techniques were used to investigate nitrogen assimilation of two alpine species
cluster roots are formed in response to low nutrient supply
(BSK12, SSP, AT2G17090) pathways are important for optimization of macronutrient uptake
arbuscular mycorrhizal and ectomycorrhizal mycelia improve acquisition of mineral nutrients which are already in solution
cation efflux family member is responsive to Mn deficiency Chlamydomonas
(ATOPT3, OPT3, AT4G16370) has been found to be dramatically up-regulated by Fe and Mn deficiency
Mn deficiency response syndrome is not very common in natural habitats
Dionaea and other carnivorous plants improve nutrient status by catching insects Dionaea muscipula
arbuscular mycorrhizal fungi (AMF) assist the plant in the acquisition of mineral nutrients (mainly phosphorus) and water
AM and ECM differ substantially in biochemical capabilities for carbon and nutrient acquisition
expression of root mass–depth profile trait in heterogeneous substrate might influence nutrient acquisition and NUE in barley genotypes
mycorrhizal fungi connect plant hosts to heterogeneously distributed nutrients
root length duration is the main driver of acquisition of immobile resources
S deficiency occurs in other crops
root system may enhance Pi uptake by arbuscular mycorrhizal symbiosis
phenotypes with fewer but longer laterals are capable of exploring a greater volume of soil accessible via mass flow of water, and therefore nitrate
increased root hair length improves phosphate acquisition Triticum aestivum
root hair enhanced crops have improved water and nutrient use efficiency
branched root system is expected to facilitate nutrient uptake
adaptation of Australian species to nutrient deficiencies has been linked to cluster roots
cluster roots enhance plant's access to other soil nutrients
rhizomatous (rhizoid-bearing) axes of early vascular plants function in mineral nutrient scavenging
root hairs are crucial for uptake of water and nutrients Arabidopsis thaliana
hyphae in mycorrhizal associations by virtue of their small diameter are able to penetrate soil microsites which are inaccessible to plant roots
perennials with sufficient carbohydrate reserves may have advantage over annuals in acquisition of immobile resources
leading embryo utilizes megagametophyte and subordinate embryos for its own nutrition Pinus sylvestris
root system architecture, morphology, and biochemistry can greatly affect ability of a plant to acquire nutrients from the soil
(ATNRAMP1, NRAMP1, PMIT1, AT1G80830) is responsive to Mn deficiency Chlamydomonas
cluster roots exude enzymes
Fe acquisition mechanisms differ between Strategy I and Strategy II plants
parasite had access to N in the substrate Rhinanthus minor
parasite forming haustoria at distal root tips is thus unable to intercept the nutrients taken up by the host's roots Rhinanthus minor
leaf demands mineral nutrients
increased mycorrhizal colonization enable plants to collect more nutrients
transpirational water fluxes play fundamental role in nutrient acquisition
water-deficit stress causes deleterious effects on nutrient uptake
mass-flow reduces rhizosphere nutrient depletion
some species of associative and endophytic diazotrophic bacteria are reported to improve nutrient uptake
cortical phenes deserve more attention for their possible influences on soil resource acquisition in maize Zea mays
AM fungi increased leaf P concentrations Vicia faba L.
Optimization of Root system architecture (RSA) may be a promising avenue to enhance nitrogen (N) uptake efficiency Triticum aestivum
cluster roots enhance plant's access to phosphorus
acquisition of immobile resources is related to root length duration
high transpirational water fluxes may be especially important in zones where roots are sparsely distributed
mutant barley lines with small rhizosheaths were compromised for P-accumulation
cytokinins is involved in nitrate uptake
inhabiting pelagic ecological niche provides advantages such as increased diffusivity of available nutrients Utricularia
economic use of nutrients is vital in extremely nutrient-impoverished and seasonally dry habitats of Banksia species Banksia
organic anion efflux from roots of P-deficient plants plays a role in P nutrition
S deficiency occurs in cereals
root cap contributes substantially to plant Pi acquisition
Rhinanthus minor abstracts carbon (C), nitrogen (N), and other minerals Rhinanthus minor
increased sunlight absorption may increase nutrient uptake
Trichoderma-induced plant growth promotion is mediated by enhanced nutrient uptake
VAM is commonly associated with enhanced phosphorus acquisition
cluster roots are a strategy for nutrient acquisition in extremely oligotrophic habitats
ericoid mycorrhizal fungi can contribute to plant nitrogen uptake
trees colonizing former grasslands may mainly exploit easily available N pools
soil P availability affects plant P uptake
rhizosphere metabolic mixture comprising soyasapogenol B, 6-hydroxynicotinic acid, lycorine, shikimic acid, and phosphocreatine enhances nutrient uptake in maize crops
lower soil microbial diversity could hinder arbuscular mycorrhizal fungi (AMF)-mediated nutrient acquisition from agricultural soils
Some work in the tropics has explored plant trade-offs for the acquisition of different nutrients
phosphorus (P) uptake was represented only in four of the models using just one parameter (P uptake rate)
floral display and reward production relies heavily on nitrogen and phosphorus
relatively greater root biomass and root production rates in infertile surface soils vs fertile surface soils is likely for rapid uptake of scarce mineral nutrients released from litter decomposition
nutrient availability can overcome cellular nitrogen (N) and phosphorus (P) costs
single-species inocula had stronger effects on foliar nutrient content
efficacy of mass-flow depends on soil nutrient retention Phaseolus vulgaris
field experiments measured nitrogen uptake Triticum aestivum
formation of extra root hairs may represent 'rescue' back-up, which is induced when the Fe deficiency response is not triggered by low availability of Fe
Arabidopsis thaliana (ATWRKY75, WRKY75, AT5G13080) has a demonstrated function in phosphate acquisition Arabidopsis thaliana
root-fungi associations is well known for facilitating plant nutrient uptake
terrestrial plant species rely on root pathway via root epidermal cells and root hairs
releasing carbon that stimulates rhizosphere microbial production of extracellular phosphatase is outsource P-acquisition strategy
arbuscular mycorrhizal (AM) fungi mainly use mineral nutrients
ECM species interact with their nutritional requirements
tip growth is essential for water and nutrient uptake
ectomycorrhizal (ECM) fungi mine forest soils for nitrogen, phosphorus, and micronutrients
natural abundances of carbon stable isotopes provided insights into possible use of H. physophora tissues as carbon source by fungus Hirtella physophora
arbuscular mycorrhizal fungi (AMF) provides mainly phosphorus (P) and nitrogen (N) to host plant
root morphological traits have been proposed as good indicator of capacity of plants to forage for resources and dependency on AMF
N addition could alleviate N resource constraints
trade-offs between plant growth and P uptake result in different root P-uptake rate (PUR)
strigolactone exudation in relation to nitrogen availability is part of plant nutrient acquisition strategy
control treatment comprised plants having free access to all nutrients including nitrogen (N) Phaseolus vulgaris
external changes in nitrate triggers nutrient uptake
'mass-flow' treatment plants had maximum concentrations at 10 mm from N source Phaseolus vulgaris
sparse lateral branching should explore a greater volume of soil than a many/short (MS) lateral root phenotype
root trait that increases the volume of soil explored may not be as effective in improving the efficiency of uptake of more mobile ions such as nitrate
high transpirational water fluxes may be especially important in acquisition of mobile nutrients
compatible, host-derived organic N compounds in the form of amino acids are not unique to legumes fixing N2 as their only N source Rhinanthus minor
mycorrhizal fungi increase nutrient absorptive surface area of host plant root systems
essential micronutrients have to be acquired in sufficient amounts by plants
sparse lateral branching should reduce competition for N among neighbouring lateral roots
overlap of N-depletion zones around roots of the same plant effectively reduces nitrate uptake efficiency
roots 10mm apart will probably compete for NO3- Zea mays
mass-flow plays no direct role in nutrient uptake across plasma membrane
magnitude of distance over which mass-flow is effective remains unknown understanding of nutrient acquisition
AM fungi and P addition increased leaf P concentrations Vicia faba L.
P is acquired within 1mm of the root surface
variation in root hair length is correlated with improved phosphorus (P) acquisition efficiency
transpirational water fluxes are up-regulated in plants grown in low-nutrient soils
plant-associated microbial communities promote plant nutrient uptake
rapid modification of their root system efficiently acquires edaphic resources
plants adapt to reduced nitrogen availability by increasing capacity for nutrient acquisition
elevated strigolactone (SL) levels in roots may contribute to increased mycorrhizal colonization
nutrient status improvement particularly affects nitrogen status Dionaea muscipula
greater lateral root branching might favour uptake of immobile nutrients like P Zea mays
nitrogen status improvement stimulates growth Dionaea muscipula
transpiration powers movement of water and dissolved nutrients to root surfaces by mass-flow
enhanced growth is commonly associated with increased phosphorous acquisition
waterlogging severely affects nutrient uptake
increase in root-hair length and density probably occurs to expand root surface area
common bean (Phaseolus vulgaris) has observed genotypic variation in phosphorus (P) acquisition and metabolic efficiency of roots under phosphorus (P) stress Phaseolus vulgaris
root cortical aerenchyma formation in axial roots is more advantageous for P capture in maize than in common bean Zea mays; Phaseolus vulgaris
maize genotypes with large number of crown roots will have greater topsoil exploration Zea mays
root biomass is root morphological adaptation to P stress
root exudate production is root physiological adaptation to P stress
elevated strigolactone (SL) levels in root exudates may contribute to increased nodulation
increased P uptake is not the main mechanism by which mycorrhiza increase attractiveness of plants to aphids Vicia faba L.; Acyrthosiphon pisum Harris
cereal root system as a whole encounters more diverse range of nutritional environments
altered root CK status may influence nutrient uptake
fewer crown roots might promote strong, long roots that efficiently promote uptake of deep water and nitrogen under dense planting
total root length is key in the acquisition of sparingly soluble elements
reduced root metabolic costs enables improved P acquisition from low-P soils
root-shoot ratio is root morphological adaptation to P stress
longer root hairs contribute more to water and nutrient uptake
mobile elements such as N are known to be acquired through mass-flow
external changes in phosphorus triggers nutrient uptake
local root development maximizes Pi interception Arabidopsis thaliana
response of root hairs to nitrate availability may be important strategy for enhanced N acquisition when plants reach nitrate-enriched soil patch
root hair length affects grain yield of barley plants Hordeum vulgare
root hair formation increases foraged soil volume
arbuscular mycorrhiza (AM) symbiosis enhances nutrient supply of plants
root hair (RH) elongation continuously increased with decreasing nitrogen (N) availabilities
organic acids acidify rooting medium
trade-off between phosphorus (P) acquisition and nitrogen (N) acquisition may demonstrate that more nodal roots are beneficial for growth in low phosphorus (P) soil but fewer nodal roots are beneficial for growth in low nitrogen (N) soil Zea mays
greater density of nodal roots in tillering species may change relationship of lateral root-branching density and resource capture Triticum aestivum; Hordeum vulgare; Avena sativa
myrmecotrophy can be of considerable benefit to nutrient budget of host plants
phosphorus addition would increase PUR
studies of nutrient acquisition have taken advantage of root hairless mutants in both cereals and crop eudicots
functional-structural modeling is utilized to explore effect of reduced secondary growth of roots on phosphorus (P) acquisition
root cortical senescence may increase P capture in monocot species
buzz mutant displays increased nitrate foraging phenotype Brachypodium distachyon
neighboring inefficient species took up Mn 2+ and soluble P mobilized by the facilitator
cryptic associations may be important component of plant nutrient relations
capacity to use nutrients from insect waste may be crucial for survival and reproduction in nutrient-deficient habitats like tropical rainforest canopy
plant Mn uptake is affected by soil microbiome
two models had some representation of symbiotic nutrient uptake, including biological nitrogen fixation (BNF) and mycorrhizal nutrient uptake
chemodiversity and composition of rhizosphere metabolites and their relationship to soil microbiome properties further impacted plant nutrient uptake Zea mays
ant–plant interactions can be enhanced by fungi
rth2 mutant showed that root architecture was regulated by low-phosphorus soils
greater stoichiometric stability is greater ability to maintain plant nutrient status despite variations in soil nutrient availability Leymus chinensis
Leymus chinensis has greater stoichiometric stability than other species in a typical steppe Leymus chinensis
root–soil contact facilitates nutrient uptake
ECM and ERM enhance nutrient uptake by plants
pOsGPX1::astol1 transgenic lines expression enhances sulphate uptake
mixed-strain inoculation treatment had generally weaker effects on foliar nutrient content
plants receive upwards of 90% of their phosphorus from associations with AMF
AM fungi have reliance on inorganic soil nutrients
vascular epiphyte morphological adaptations enable nutrient uptake from clouds, rainfall, throughfall and stemflow water
citrus rhizosphere microbiome mediate rhizosphere plant–microbe and microbe–microbe interactions for nutrient uptake Citrus
evolutionary shift from AM to EcM is linked to plant nutrient acquisition strategies through the specific type of mycorrhizal association
fungal partners provide essential nutrients such as nitrogen, phosphorus, and micronutrients
species with larger genomes have higher phosphorus (P) demands
positive plant–soil feedback loop allows trees to access and monopolize otherwise inaccessible N pool
endocytosis includes pinocytosis of fluids and solutes
broad-spectrum antifungal activity of Bg_9562 enables bacterium to access fungal biomass as nutrient source Burkholderia gladioli
reprogramming of root development improves nitrogen (N) acquisition
inorganic phosphate (Pi) is essential mineral nutrient for plants
maize recombinant inbred lines (RILs) with contrasting crown root number (CN) were compared under contrasting P availability Zea mays
increased root branching may promote resource acquisition
AM fungi increase plant uptake of phosphorus
intercropping enhances maize nutrient uptake
mycorrhizal pathway can contribute more than half of plant nutrient uptake
neopolyploid growth and fitness requires greater nutrient supplies than diploid progenitors
Bg_9562 is deployed to forage over fungi Burkholderia gladioli
low nutrient conditions should trigger increase in biomass allocation to roots
Caularthron bilamellatum obtains nutrients from ant waste Caularthron bilamellatum
nutrient cycling conservation occurred either by directly releasing enzymes for nutrient foraging
arbuscular mycorrhizal fungi (AMF) enhance plant nitrogen (N) acquisition
plant Mn uptake is affected by soil Mn availability and plant strategy
higher C investment in ectomycorrhiza associations could lead to lower nutrient absorption capacity woody plant species
increased specific root length (SRL) may promote resource acquisition
decreased root tissue density (RTD) may promote resource acquisition
biodiversity of key microbial ecological clusters in intercropping systems in turn affects crop nutrient uptake
arbuscular mycorrhizal fungi (AMF) inoculation modified nutritional content of foliar tissues
decreased root diameter (RD) may promote resource acquisition
Root enzyme activities (e.g. phosphatase and protease) function to release mineral nutrients from organic matter
tropical epiphyte obtains nitrogen from activity of mutualistic ants Caularthron bilamellatum
epiphytic orchid C. bilamellatum sacrifices approximately 50% of volume of water storage tissues in pseudobulbs Caularthron bilamellatum
terrestrial plant species rely on mycorrhizal pathway via arbuscular mycorrhizal (AM) fungal hyphae
putative cyclin-dependent kinase (CDK)-like gene is a new player in nitrate-responsive root architecture Brachypodium distachyon
ants provide several benefits including contributing to nutrient needs of host plant
root NSC concentrations of C3 and C4 species may respond differently to P availability
pests' successful colonization relies on obtaining sugars and amino acids
Pi fertilizer supply only 15%-25% is taken up by plants plant uptake efficiency
Iron (Fe) is essential nutrient
stomatal closure leads to reductions in nitrogen uptake
Plasmodium falciparum and Toxoplasma gondii are known to use different set of genes to undertake endocytic nutrient uptake Plasmodium falciparum; Toxoplasma gondii
plant pathogens and insect pests need to get sugars and other nutrients from their hosts
root elongation inhibition affects uptake of water and nutrients
Piriformospora indica significantly improves nutrient uptake Hordeum vulgare
root hairs (RHs) provide nutrient uptake enhancement
root hairs facilitate water/nutrient uptake
root hairs facilitate uptake of water and macronutrients
Pseudomonas syringae during foliar infection may simply intercept quaternary ammonium compounds (QACs) available in the apoplast
roots serve nutrient and water uptake
62 significant QTL detected for plant phosphorus (P) uptake Brassica napus
miR166- HD-ZIPIII module plays critical roles in nutrition ion uptake
activation of soil P by phosphatases enhances plant P uptake
soil salinization interferes with nutrient and water uptake
uq.C3b identified specifically for phosphorus (P) uptake Brassica napus
membrane transport proteins play a central role in nutrient uptake from soil Arabidopsis thaliana
initial haustoria transfer nutrients
root hair development significantly affects nutrient absorption
adaptive responses help plants acquire and utilize Pi (inorganic phosphate)
arbuscular mycorrhizal (AM) fungi provide phosphorous and micronutrients
capacity to use nutrients from insect waste may be crucial for survival and reproduction for plants with arboreal lifestyle
long-lived and rather costly roots capture nutrients for the longest possible period
ectomycorrhizal association may favor in low soil fertility regions
ion transport is involved in plant nutrition
root access to soil nutrients is critical yield-limiting factor
enhanced root growth might contribute to improved extraction of nutrients from soil
arbuscular mycorrhizal (AM) fungi is attracted to host plants in order to obtain necessary nutrients
seminal roots is important for phosphorus acquisition Zea mays
pathogenic biotrophic fungi differ in nutritional strategies
root system architecture (RSA) links to nutrient uptake
root development and microbial symbiosis exploit soil nutrients
parasitic plants employ haustoria
abiotic stress negatively affects nitrate uptake by roots
greater root growth improves the capture of deep nitrate
functional-structural plant model SimRoot is used to determine relationship between secondary growth of roots and phosphorus (P) acquisition
N, P, and water are three primary soil resources that limit plant growth in most soils
glucose content in infected roots have been found to significantly increase in late stages of infection Plasmodiophora brassicae
leaf [Mn] did not change in HP treatment
arbuscular mycorrhizal fungi (AMF) rob nutrients from nonhost plants
small cell size (less than 1 μm) allows effective capture of nutrients and light Prochlorococcus spp.
persistence of root cortical tissue has implications for P capture
increased root length density in the subsoil under drought and N-deficient conditions resulted in improved water and N acquisition and plant growth Zea mays
small crown root number (CN) was beneficial for N acquisition Zea mays
plants acquire sulfur from soil
common bean (Phaseolus vulgaris) productivity in Africa and Latin America is often limited by low phosphorus (P) availability Phaseolus vulgaris
root longevity affects resource capture
phosphate (Pi) is essential macronutrient
mycoheterotrophic plants partly or completely rely on other organisms
lateral roots (LRs) promotes efficient uptake of deficient nutrients
altered response to P and S availability may have contributed to increased uptake of P and S Hordeum vulgare
increased expression of genes encoding transporters for phosphate, sulfate, Mn, and Zn could make a relevant contribution to increased element accumulation Arabidopsis thaliana; Hordeum vulgare
genotypes with reduced secondary development have greater P capture from low-P soils Phaseolus vulgaris
CN is important regulator in soil resource capture by lateral roots and root symbionts Zea mays
greater topsoil exploration will result in better P acquisition Zea mays
super-root transgenic barley plants displayed increased accumulation of other low-mobility nutrients Hordeum vulgare
mycorrhized roots provide phosphorous and micronutrients
spatiotemporal dynamics of topsoil foraging affects acquisition of P
altered root exudation of element-mobilizing compounds may play a role in enhanced element acquisition
intraplant competition is quite small for P acquisition
optimum range of crown root number (CN) is likely to be greater in soils of low P availability Zea mays
plants acquire sulfur as inorganic sulfate anion
anatomical phenes that reduce the metabolic cost of soil exploration should have benefits for capture of both mobile and immobile resources Zea mays
plant roots perform water and nutrient uptake
factors affecting costs and benefits of axial root production for P capture can result in different strategies to improve P acquisition
P acquisition occurs mostly less than 1 mm from surface of a root
altered interaction of CK-deficient roots with root microbiota may play a role in enhanced element acquisition
total root surface area is root morphological adaptation to P stress
greater root depth results in increased subsoil foraging for water or N Zea mays
versatility in the regulation of nutrient-responsive hormone pathways enables plants to simultaneously coordinate morphological and physiological responses to improve nutrient acquisition
inorganic phosphate (Pi) is delivered to host plant
root hairs is important for phosphorus acquisition Zea mays
physiological functions define macronutrient uptake efficiency
soil nutrient level strongly influences mycorrhizal pathway contribution to plant nutrient uptake
phenotypic plasticity of root hairs is important for nutrient uptake and plant growth
fungal partners obtain nutrients from surrounding soil
two Glc-mediated mechanisms influence nitrate uptake
biotrophic and hemibiotrophic fungi evolved haustoria
core microbiome including Pseudomonas, Agrobacterium and Cupriavidus showed traits of microbial function mediating nutrition uptake
endocytosis includes phagocytosis of solid food particles
P deficiency may trigger alternative P-acquisition strategies
species with large genomes have higher demands for phosphorus and nitrogen
AM and rhizobial symbioses have synergistic effects on plant performance
plants actively seek and mine inorganic phosphate (H2PO4− or Pi)
root hair (RH) elongation facilitates nitrogen (N) acquisition
strigolactones (SLs) reallocate resources from shoot to root nutrient absorption
lateral roots (LRs) function in nutrient uptake
greatly reduced cuticle in white basal part of leaves could enable nutrient uptake Isoetes australis
lateral roots contribute significantly to the acquisition of P, Mn, and Zn Oryza sativa
maize lines with small crown root number (CN) had greater nitrogen (N) acquisition under low-N conditions Zea mays
lateral root branching enables increased topsoil foraging
improved topsoil foraging resulted in greater P acquisition Phaseolus vulgaris
necrotrophic pathogens use nutrients derived from dead host plant tissue
slow NH4+ uptake rate in Nepenthes ampullaria is not unexpected given longevity of pitchers Nepenthes ampullaria
greater shoot biomass occurred in low-P soil Phaseolus vulgaris
small crown root number (CN) was beneficial for N and water acquisition in conditions of suboptimal N availability Zea mays
ability to explore greater soil volumes enables phosphorus acquisition
long-lived and rather costly roots capture nutrients
different P-use efficiency of C3 and C4 photosynthetic pathways causes different responses of root NSC concentrations to P availability
plant diversity enhances nutrient uptake
There are very few empirical data linking root water and nutrient acquisition strategies in tropical forests but there have been advances in identifying clusters of root traits for nutrient acquisition
nutrients are sequestered by absorbing the excrement of predatory insects that live on sticky leaves of Roridulaceae
AM fungi (AMF) improve plant nutrition with mineral nutrients
accumulation of the same type of elements in leaves suggests that their acquisition depends on common mechanisms that appear to be evolutionarily stable Arabidopsis thaliana; Nicotiana tabacum; Hordeum vulgare
total root length is root morphological adaptation to P stress
increased Pi uptake following nitrate treatment suggests interdependence of N and P acquisition
larger soil volume exploited by the enhanced root system of CKX-overexpressing plants besides this, additional factors must play a role in element accumulation Hordeum vulgare
increased root length density enables increased topsoil foraging
CWDEs have nutritional role by providing carbohydrates from the plant cell wall
nitrogen and phosphorus acquisition is balanced interdependent requirements of nitrogen and phosphorus
rootless 'pelagic' Utricularia could enable to grow and utilize both inorganic and organic nutrients (either dissolved or particulate, i.e. from plankton as well as detritus) in water column Utricularia
Nepenthes ampullaria must perform balancing act between creating optimal conditions for micro-organism-derived nitrogen mineralization and digestion of animal-derived nitrogen species Nepenthes ampullaria
higher surface area of the root conferred by increases in the number and length of root hairs improves Pi acquisition efficiency Arabidopsis thaliana
shallow growth angles are more beneficial for the capture of immobile resources in the topsoil, such as phosphorus
root hair elongation is required for nutrient uptake Arabidopsis thaliana
arbuscular mycorrhizal (AM) fungi facilitate the acquisition of phosphorus
PTR via ToxA activity may increase access to nutrients
root phenes associated with enhanced topsoil foraging are important for P acquisition
specific root surface area is root morphological adaptation to P stress
utility of axial root number of Poaceae species for P capture in low-P soil is uncertain
intermediate number of crown roots may be ideal to cooptimize acquisition of mobile and immobile resources Zea mays
greater density of nodal roots in tillering species may change relationship of nodal root occupancy and resource capture Triticum aestivum; Oryza sativa; Hordeum vulgare; Avena sativa
increasing resource allocation to root growth improves phosphorus (P) acquisition
diffusion of phosphorus (P) in soil is greatly outpaced by plant uptake
axial roots of monocot crops generally produce fewer root exudates capable of solubilizing P pools in rhizosphere
AMT1-STOP1 module sustains plant growth
reduced nodal root number (NRN) hypothesized to increase N acquisition in low N environments Zea mays
proteoid roots secrete organic acids and protons
flavonoid chemoattraction of rhizobia and mycorrhizal fungi secures nutrient supply to host plants
reduced inter- and intraplant competition for internal and external resources increases root depth and acquisition of deep soil resources
root hairs are important for water and nutrient uptake
morphological change in root growth angle is thought to enable efficient absorption of Pi from topsoil Arabidopsis thaliana
rhizobial symbiotic mutants (AtLYK3, LYK3, AT1G51940) nfp, and ipd3 exhibit increased phosphorus content Medicago truncatula
limited phosphate (Pi) availability in soil triggers increased root hair density
Pseudomonas syringae is adapted to import choline
uq.C3a identified specifically for phosphorus (P) uptake Brassica napus
primary metabolites function as nutrient source of carbon and nitrogen for microbes
induction of the complex Fe starvation syndrome of strategy I plants will mobilize Mn in addition to Fe
mass-flow may partially substitute for root density Phaseolus vulgaris
plant growth and development must be coordinated with nutrient uptake
increased root hair number and length enlarges root-soil surface