Notice: Database construction is still in progress. Certain features may be incomplete, slower than usual, or temporarily unavailable while we re-ingest the knowledge graph with citation data. Thank you for your patience.
← All pathways

plant growth

38945 relationships annotated with this phrase. Showing first 500 of 38945.
Source entity Relationship Target entity Species
dry organ weight did not reveal any impact of slskor mutation on plant growth Solanum lycopersicum
SKRP mutants do not illustrate visible growth penalty Arabidopsis thaliana; Glycine max
miR156 overexpression strongly reduced stalk length Nicotiana attenuata
OsHMGB1 regulates expression of growth-related genes Oryza sativa
fungicide application increased plant biomass
predicted increases in vapour pressure deficit (VPD) are expected to influence vegetation growth globally
phosphorus addition shows no significant change in root biomass of Cleistogenes squarrosa Cleistogenes squarrosa
biomass (BM) was consistently lower across all 3 years
expression lines were grown on medium containing DMSO, 50 or 100 μM Dex Arabidopsis thaliana
fast-growing stage (22–24 d) root exudates enhance plant growth-related genes Arabidopsis thaliana
mutual modulation of root activities by plants and soil microbiomes through metabolic processes ultimately influences plant productivity
larger cell sizes may reduce growth rates
tpTOC75 lines developed smaller mature rosettes Arabidopsis thaliana
copper (Cu) deficiency does not produce changes shoot or root biomass Arabidopsis thaliana
irAGO7 and WT plants produced similar numbers of leaves with similar chlorophyll contents Nicotiana attenuata
radicle is required to initiate postembryonic plant growth Arabidopsis thaliana
photosynthetic rates and carbon assimilation constraints impact biomass allocation among plant organs
pOsGPX1::astol1 transgenic lines display similar tiller number Oryza sativa
plant biomass has positive relationship with middle growing-season precipitation amount
OsEPF1oe plants were physically smaller Oryza sativa
(PPR1, AT1G06580) mutant has 30% lower fresh weight (FW) than wild-type (WT) plants after Cd treatment Arabidopsis thaliana
F2 plants were transferred to medium with different Dex concentrations Arabidopsis thaliana
four specific QTLs on chromosomes 1, 2, and 8 identified at distinct time points during the plant's growth Zea mays
zcn8 and rap2 genes, when interacting with each other and mads69 circuitously regulate plant height Zea mays
pepper-unique nonantagonistic core microbiota could have been beneficial for pepper growth only in 2015 during the rotation season
NAC094-overexpressing plants (NAC-OE1 and NAC-OE2) exhibit reduced shoot biomass Lotus japonicus
site with highest vapour pressure deficit (VPD) is expected to have lower growth rates
rosettes of irAGO7 and WT plants grew similarly each other Nicotiana attenuata
decadal soil warming decreased production of aboveground biomass
arid and semiarid regions are regions where most C3 and C4 crops cannot grow or are limited to short and unpredictable rainy seasons
fungicide application did not significantly affect individual size
nia1nia2 mutants showed significant growth reduction compared with WT plants (Col-0) Arabidopsis thaliana
plants with larger genomes may enhance plant growth performance under possibly low water availability
relative growth rate (RGR) will have negative relationship with genome size (GS)
seasonal redistribution of precipitation severely limits vegetation development
(CLF, ICU1, SDG1, SET1, AT2G23380) mutants exhibit dwarf stature Arabidopsis thaliana
ZmBELL10-OE plants exhibit increased ear height Zea mays L.
Weibull model can fit temporal plant height
larger cell size associated with larger genome size (GS) may provide environment-dependent growth advantages
oastlAC B +/+ mutant shows decreased shoot biomass Arabidopsis thaliana
zmbell10-1 mutants have decreased plant height Zea mays L.
Pseudomonas is well-known for stimulation of root growth
plants with larger genomes may enhance plant growth performance under low growth temperatures
oastlAB C +/+ mutant shows decreased fresh weight by 45% at 4 weeks and 74% at 8 weeks compared to wild type Arabidopsis thaliana
arbuscular mycorrhizal (AM) Medicago truncatula has higher root and shoot biomass Medicago truncatula
FTSZ1-16 line shows lower total dry weight under field conditions Nicotiana tabacum
monoterpene mixture at 6.25 mM applied at 7 dpi causes decrease in shoot fresh weight Populus tremula × alba
maize crops grown in sterilized soil showed narrower leaf widths
heat-treated plants did not differ from in leaf number Brassica rapa
enhancement of early growing-season normalized difference vegetation index (NDVI) may have legacy effects and compensate for negative impacts on plant growth
(AT.EIF4E1, CUM1, EIF4E, eIF4E1, AT4G18040) mutants display decreased fresh weight Arabidopsis thaliana
OXrPPR1 plants accumulate higher fresh biomass than wild-type (WT) plants after Cd treatment Arabidopsis thaliana
OE plants exhibited significantly thicker thalli than Tak-1 Marchantia polymorpha
genes are mainly involved in plant growth and responses to pathogen and abiotic stress Fragaria vesca
oastlBC A +/+ mutant shows no difference from wild type Arabidopsis thaliana
(VUP1, AT3G21710) 1-165 and 1-126 truncated versions lead to similar phenotypes to full-length (VUP1, AT3G21710) overexpression Arabidopsis thaliana
(S8H, AT3G12900) Ox lines showed significantly higher shoot fresh weight Arabidopsis thaliana
M24 overgrowth mutant line is taller than wild-type Anhinga
Beyma mutant exhibited slower growth rate Lotus japonicus
forests growing under higher vapour pressure deficit (VPD) are expected to have lower relative growth rates
(AT.EIF4E1, CUM1, EIF4E, eIF4E1, AT4G18040) mutants show lower height Arabidopsis thaliana
mutant stigmas of (GOM8, RHD3, AT3G13870) (RL2, AT5G45160) when pollinated with pollen from wild type exhibit normal growth Arabidopsis thaliana
substantial losses of soil N explained reduced productivity, both aboveground and belowground
below and aboveground plant productivity in this subarctic grassland ecosystem was more affected by warming-induced change in soil N than by the warming per se
fungicide application inhibited the growth of conspecific larger individuals conspecific larger individuals
modeling temporal trajectories of NGRDI indices demonstrated effectiveness for enhancing our understanding of plant growth dynamics
arbuscular mycorrhizal fungi (AMF) increase plant height
(ATGT18, GT18, XLT2, AT5G62220) deficient mutants show minor, if any, growth phenotypes under laboratory conditions Arabidopsis thaliana
Athda7-2 mutant exhibits defects in postgermination growth Arabidopsis thaliana
calcium (Ca) deficiency increases shoot and root fresh weight Arabidopsis thaliana
plant height is positively correlated with plant biomass
plasticity of metabolic reactions affects plasticity in fresh weight (FW), as a proxy for growth Arabidopsis thaliana
predicted productivity of hypothetical 6-yr plantation at Tequila was 28.5 Mg ha-1 Agave tequilana
predicted optimal angle of lowest (oldest) leaf increases with canopy size Agave tequilana
FTSZ1-16 line shows lower plant height under field conditions Nicotiana tabacum
The biomass of (ELMOD_B, MCR, AT2G44770) seedlings treated with only malathion was not significantly different from the untreated controls Amaranthus tuberculatus
(ATFT1, ATFUT1, FT1, FUT1, MUR2, AT2G03220) deficient mutants show minor, if any, growth phenotypes under laboratory conditions Arabidopsis thaliana
coi1a mutants show no difference in plant height compared to WT plants in the field Oryza sativa
shifts in fungal community composition related to plant biomass
efficiency of 0.0069 would result in productivity of c. 1.56 kg m-2 yr-1, or 15.6 Mg ha-1 annualized over 8-yr growth cycle Agave tequilana
pOsGPX1::astol1 transgenic lines display similar panicle number Oryza sativa
(AtHMGB1, HMGB1, NFD1, AT3G51880) mutant seedlings showed slightly weaker growth compared with WT seedlings Oryza sativa
bdgux2 mutant plants grew similar to wild-type Brachypodium distachyon
deep-rooted forb species result in slight enhancement in plant growth
MADS box and UspA gene mutants found no significant difference in root growth and fresh weight compared with wild type Arabidopsis thaliana
stem growth is either a result of cell elongation or cell elongation and cell division
RNAi plants with lower levels of LPLA were heavily impaired in normal air Arabidopsis thaliana
analysis starting at day 17 captures growth attributes over approximately 92% of plant growth Setaria
wild-type plants harvested after 4 weeks
plant biomass correlates with stomatal size (SS) Oryza sativa
plants with low stomatal density (SD) and large stomatal size (SS) typically had higher biomasses Oryza sativa
eIF4E1-OE plants exhibit higher height Arabidopsis thaliana
warming in cold grasslands expected to increase fine root productivity
PDV2-9 × PDV1-9 line shows lower leaf area under field conditions Nicotiana tabacum
bark contributes predominantly to stem diameter variations
pOsGPX1::astol1 transgenic lines show no significant difference in straw biomass Oryza sativa
BR biosynthesis mutations exhibit stunted stature
decrease in total growing season fine root production under warming was mainly attributable to decreased soil N
genes related to growth ( (ATHB-2, ATHB2, HAT4, HB-2, AT4G16780) (ATEXP8, ATEXPA8, ATHEXP ALPHA 1.11, EXP8, EXPA8, AT2G40610) and (XTH15, XTR7, AT4G14130) ) were upregulated in (PAP3, PIF3, POC1, AT1G09530) overexpression transgenic plants Arabidopsis thaliana
arbuscular mycorrhizal fungi (AMF) has effect on vegetative biomass
phosphorus (P) deficiency decreases shoot fresh weight Arabidopsis thaliana
phosphorus (P) deficiency decreases root fresh weight Arabidopsis thaliana
irAGO7 plants continued to lag behind WT counterparts Nicotiana attenuata
variations in stem diameter would depend on tissue properties and their respective proportions
systemic expression of Avr9B-like protein from Stemphylium lycopersici in MM-Cf-0 tomato plants triggered stunted growth Solanum lycopersicum
variation in stem diameter (SD) was largest across species Vaccinium angustifolium; Vaccinium myrtilloides
35s::AHB1 mutants displayed similar growth to 35s::GSNOR1 mutants Arabidopsis thaliana
ZmReas1 mutation causes slow growth phenotype Zea mays
(AtNPF1.2, NPF1.2, NRT1.11, AT1G52190) (NRT1.12, AT3G16180) double mutants showed no increase of growth in younger leaves when nitrate concentrations were increased Arabidopsis thaliana
concerted action of different histone deacetylases (HDACs) controls Arabidopsis growth Arabidopsis thaliana
stalk lengths of irAGO7 plants were significantly shorter than stalk lengths of WT plants Nicotiana attenuata
MYC interacts with growth-promoting factors
PDV2-9 × PDV1-9 line shows lower plant height under field conditions Nicotiana tabacum
annual plants can grow and reproduce when water and nutrients are scarcer
(ALKBH10B, AT4G02940) mutants affect vegetative growth Arabidopsis thaliana
plants expressing relevant markers are grown for 7 days Arabidopsis thaliana
PDV2-9 × PDV1-9 line shows lower total dry weight under field conditions Nicotiana tabacum
bdxax1b mutant plants do not exhibit growth phenotype Brachypodium distachyon
plants with larger genomes may enhance plant growth performance under high soil fertility
rhd3-8 mutant exhibits small rosette Arabidopsis thaliana
Sapur.001G016500 is (SLO1, AT2G22410) homolog, slow growth 1 Salix purpurea
additional robustness under stress conditions ensures coordinated growth within and between tissues
HMGB1-OE seedlings were noticeably smaller under Pi-sufficient (HP) and Pi-limited (LP) conditions in glasshouse Oryza sativa
soybean FBA model predicts soybean growth rates that fall within the experimentally determined range of 0.05 − 0.1 g g − 1 DW d − 1 Glycine max
(MIR399, MIR399F, AT2G34208) overexpression did not influence stalk length Nicotiana attenuata
increasing water temperature impairs above-ground biomass
prolonged vegetative growth in SbGhd7 overexpression lines results in more than twofold biomass accumulation Sorghum bicolor
relative growth rate (RGR) under tropical (control) conditions will have negative relationship with genome size (GS)
lowered chaperone activity in distant tissues results in coordinated decreased growth Arabidopsis thaliana
WT plants had greater shoot fresh and dry masses Nicotiana attenuata
ov473 and ovPN59 plants were shorter Nicotiana attenuata
(BRD1, AT1G20670) gene was also discovered to influence plasticity of plant height Zea mays
dtn1-1 mutant exhibits shorter plant height Oryza sativa
(APX3, AT4G35000) and (APX4, TL29, AT4G09010) co-silencing does not cause growth differences Oryza sativa
(AXY4, TBL27, AT1G70230) deficient mutants show minor, if any, growth phenotypes under laboratory conditions Arabidopsis thaliana
low SD and large SS plants were physically larger Oryza sativa
reduced soil N stock likely counteracted positive effect of the more benign soil thermal environment on vascular plant production
decadal soil warming decreased fine roots
model has not performed continuous simulation for entire growth period
rNAD-ME1 plants had significantly lower above-ground dry weight Kalanchoe fedtschenkoi
silencing of NbPAT resulted in strong growth reduction Nicotiana benthamiana
gradient of a growth signal from the apex may include auxin or photoassimilates Brassica rapa
pin quadruple mutant (ATPIN1, PIN1, AT1G73590) ;3;4;7 is dwarfed Arabidopsis thaliana
(ATGRP8, CCR1, GR-RBP8, GRP8, RBGA6, AT4G39260) ProSNBE lines have primary inflorescence stem height approximately 2-fold higher than (ATGRP8, CCR1, GR-RBP8, GRP8, RBGA6, AT4G39260) mutants Arabidopsis thaliana
Leu-rich repeat extensins (LRXs) are required for plant growth
double suppression of GmEXPB2 and GmINS1 resulted in decreases in biomass Glycine max
5-d-old seedlings of corresponding expression lines were transferred to medium containing 50 or 100 μM Dex Arabidopsis thaliana
slow rate at which Agave tequilana expands to cover ground after planting results from low overall productivity Agave tequilana
Mp glk mutants show differences in thallus size Marchantia polymorpha
(VUP1, AT3G21710) OX plants exhibit severe dwarf phenotype at rosette stage Arabidopsis thaliana
NahG transgene had no impact on growth phenotype of (CYP98A3, REF8, AT2G40890) plants Arabidopsis thaliana
rNAD-ME1 had dry weight vegetative yield measured for plants grown in greenhouse Kalanchoe fedtschenkoi
flux through OPPP is required for growth responses to nitrate Arabidopsis thaliana
sir1-1 cad2-1 double mutant (s1c2) grows faster than sir1-1 mutant Arabidopsis thaliana
three GmINS1 OX lines have 29.5%, 62.3%, and 98.8% increases in plant dry weight
ov398 plants were initially smaller than EV Nicotiana attenuata
phosphorus addition at P12.5 significantly decreases root biomass of Leymus chinensis Leymus chinensis
(ADH, ADH1, ATADH, ATADH1, AT1G77120) control plants continued to grow normally Arabidopsis thaliana
fungicide application promoted the growth of conspecific smaller individuals conspecific smaller individuals
O-acetylserine(thiol)lyase isoform C (OAS-TL C) loss-of-function mutant is only single oastl knockout mutant that displays significant growth phenotype Arabidopsis thaliana
transfer DNA mutant in (AtMUR3, KAM1, MUR3, RSA3, AT2G20370) shows impaired growth Arabidopsis thaliana
(VUP1, AT3G21710) S119A; S120A variant overexpression results in slight dwarfism at seedling stage Arabidopsis thaliana
young leaves of dexamethasone (dex)-induced (CYP98A3, REF8, AT2G40890) pOpON grew bigger than young leaves of uninduced (CYP98A3, REF8, AT2G40890) pOpON Arabidopsis thaliana
rPPDK1 had average percentage of dry weight reduction of 34% Kalanchoe fedtschenkoi
Mutants of (ATTRX H1, ATTRX1, TRX1, AT3G51030) grew more slowly than wild type under either control or stress conditions Arabidopsis thaliana
LPLA RNAi plants showed slow leaf and root growth Arabidopsis thaliana
kinG mutant showed no obvious defects in growth or overall appearance Arabidopsis thaliana
Haberlea rhodopensis plants grown under optimal conditions gain fresh weight Haberlea rhodopensis
large-CN phenotype under P deficiency has 44% greater shoot biomass in greenhouse
plates were transferred to Percival growth chamber Arabidopsis thaliana
region of the epicotyl that displayed the greatest change in growth was localized 5 to 20 mm below the apex apex Vigna sinensis
localization of the growing region specifically to 5 mm or more below the apex in V. sinensis epicotyl and in bean hypocotyl may be due to species specificity, a lack of resolution in defining the hypocotyl regions most sensitive to growth, or a difference in using excised epicotyl/hypocotyl explants Vigna sinensis; Phaseolus vulgaris
YFP-GS line 1 displayed significantly improved growth compared with (ATSS4, SS4, SSIV, AT4G18240) mutants Arabidopsis thaliana
transgenic plants with ABA biosynthesis rescued in guard cells restores stunted growth phenotype Arabidopsis thaliana
Δ ftsZ3 mutants show growth retardation Physcomitrella patens
failure to accelerate the rate of starch synthesis in short days in GlgC-TM plants was accompanied by growth rates substantially reduced relative to wild-type plants Arabidopsis thaliana
transformants expressing C-terminal region of (ATSS4, SS4, SSIV, AT4G18240) (YFP-SS4C lines) grew better than (ATSS4, SS4, SSIV, AT4G18240) mutants Arabidopsis thaliana
loss-of-function (FBL17, AT3G54650) mutants showed greatly impaired growth Arabidopsis thaliana
higher Pi levels in roots of transgenic plants could be due to reduced shoot growth Arabidopsis thaliana
Beyma mutant resulted in smaller plant than MG-20 Lotus japonicus
isa1isa2 mutant grew slightly slower than Col-0 wild type Arabidopsis thaliana
(AGL15, AT5G13790) (AGL18, AT3G57390) (AGL24, AT4G24540) (AGL22, FAQ1, SVP, AT2G22540) mutants are small relative to wild type Arabidopsis thaliana
hypocotyl growth in B. rapa occurs in a basipetal gradient basipetal gradient Brassica rapa
sir1-1 cad2-1 double mutant (s1c2) grows 5 times faster than sir1-1 mutant under nonstressed conditions Arabidopsis thaliana
plant height and dry weight biomass showed statistically significant differences between wild-type and ca1ca2 mutant plants Zea mays
(CESA4, IRX5, NWS2, AT5G44030) mutants are able to grow healthier and more closely resemble wild-type plants Arabidopsis thaliana
rPPDK1 plants had significantly lower above-ground dry weight Kalanchoe fedtschenkoi
erect leaf rice mutant osdwarf4-1 can improve biomass production Oryza sativa
sir1-1 cad2-1 double mutant (s1c2) does not completely restore to wild-type growth levels Arabidopsis thaliana
(ADT3, PD1, AT2G27820) /4/5/6 plants displayed diminished growth relative to wild-type plants Arabidopsis thaliana
plant size exhibits strong correlation with fresh and dry weight Setaria
transgenic plant produced more biomass Arabidopsis thaliana
0.5 MS medium used for growing Col (WT) seedlings Arabidopsis thaliana
above-ground biomass was increased independently of whether they were grown under day lengths of 8, 10 or 12 h OE lines Solanum andigena
axs1-2 axs2-2/+ mutants has more severe dwarf phenotypes on growth compared with axs1-1 axs2-1/+ mutants Arabidopsis thaliana
(ARA1, ATISA1, ISA1, AT4G16130) mutant grew slightly slower than Col-0 wild type Arabidopsis thaliana
LPLA RNAi lines show growth retardation of rosettes and roots Arabidopsis thaliana
(ATGRP8, CCR1, GR-RBP8, GRP8, RBGA6, AT4G39260) mutants are severely dwarfed
(ATGRP8, CCR1, GR-RBP8, GRP8, RBGA6, AT4G39260) -6 ProSNBE lines with siliques removed become equal to wild-type plants in total stem biomass Arabidopsis thaliana
salicylic acid (SA) regulates biomass Arabidopsis thaliana
GH1-HMGA1 mutants exhibit growth defects Arabidopsis thaliana
ABA may parallel the role of ABA in promoting general plant growth
genotypes with reduced cortical cell file number (CCFN) under water stress have better growth Zea mays
OsmiR396d-resistant form of OsGRF6 transgenic plants (rGRF6OE) had slightly increased plant height Oryza sativa
mature Columbia-0 (Col-0) rosettes grown in controlled environment Arabidopsis thaliana
increased subsoil foraging for water or N results in improved plant growth Zea mays
plants were kept in Conviron growth chambers Arabidopsis thaliana
(AGL15, AT5G13790) (AGL18, AT3G57390) (AGL24, AT4G24540) (AGL22, FAQ1, SVP, AT2G22540) (AGL20, ATSOC1, SOC1, AT2G45660) plants are larger at floral transition than (AGL15, AT5G13790) (AGL18, AT3G57390) (AGL24, AT4G24540) (AGL22, FAQ1, SVP, AT2G22540) plants Arabidopsis thaliana
OsGRF6 antisense transgenic plants (GRF6as) were moderately reduced compared with wild-type (ZH10) plants Oryza sativa
albino F1 plants from (EMB2279, EMB88, SOT5, AT1G30610) × -2 cross could turn a bit green when growing on the medium but could not survive after transfer to the soil Arabidopsis thaliana
(ATGRP8, CCR1, GR-RBP8, GRP8, RBGA6, AT4G39260) ProSNBE lines showed strong increase in total stem biomass
Spinach (Spinacia oleracea var. Lina) grown under 8/16-h light/dark cycles Spinacia oleracea
growth at night decreases progressively as the photoperiod is shortened Arabidopsis thaliana
P stress reduces shoot biomass
tpTOC75 lines grew more slowly than wild type on soil Arabidopsis thaliana
tpTOC75 lines grew more slowly than wild type on plates Arabidopsis thaliana
ospp18 mutant shows no significant difference in growth compared with wild-type plants Oryza sativa
lines with large cortical cell size (CCS) have greater shoot biomass under water stress in mesocosms by shoot biomass Zea mays
double mutants from F2 families were significantly shorter than siblings Zea mays
faster myosin expression leads to larger plant size Arabidopsis thaliana
larger infection cells promoted plant biomass Glycine max
pfd mutants show reduced size Arabidopsis thaliana
mature tobacco plants grown in pots containing 3:1 (v/v) Levington M3 compost and vermiculite Nicotiana tabacum
potassium (K) deficiency decreases shoot and root biomass Arabidopsis thaliana
PhyB-1 pro35S:VUP1 plants exhibit severe dwarfism similar to (VUP1, AT3G21710) OX in wild-type plants Arabidopsis thaliana
dexamethasone (dex) induction starting at later times did not relieve much of growth inhibition of primary shoots Arabidopsis thaliana
(ATRAPTOR1B, RAPTOR1, RAPTOR1B, AT3G08850) lines are highly sensitive to applied growth conditions Arabidopsis thaliana
actinic light intensity of about 120 µmol photons m−2 s−1 is less than one-half light intensity used to grow plants Arabidopsis thaliana
the (CESA4, IRX5, NWS2, AT5G44030) D XD and TE D mutant plants grow substantially larger and can reach almost twice the height of the corresponding (ATCESA7, CESA7, IRX3, MUR10, AT5G17420) mutants
increased net rate of photosynthesis is positively associated with growth and yield of crop plants
(PFD3, AT5G49510) mutant has fresh weight approximately 75% of wild-type plants under control conditions Arabidopsis thaliana
wtBSMV-infected plants continued to grow and produce leaves and new shoots Zingiber officinale
sec24a-2 lgo-1 double mutant remains dwarfed Arabidopsis thaliana
old leaves of dexamethasone (dex)-induced (CYP98A3, REF8, AT2G40890) pOpON showed little dex-induced growth increase growth Arabidopsis thaliana
SS4N-GS-expressing plants displayed near-normal growth rates
decreased Target of Rapamycin (TOR, AT1G50030) activity in sir1-1 mutant explains retarded growth phenotype of sir1-1
multiple genes associated with auxin signaling and cell growth were found from noncanonical genes Arabidopsis thaliana
iop1 mutants stayed significantly smaller during their entire lifespan plant size Arabidopsis thaliana
mir plants had root length reduced by 24% compared to WT plants grown in presence of Fe
SmVUP1 overexpressors died quickly after germination most plants Arabidopsis thaliana
Arabidopsis plants were grown under high-irradiance white light for 2 weeks Arabidopsis thaliana
(ATGRP8, CCR1, GR-RBP8, GRP8, RBGA6, AT4G39260) ProSNBE lines have increase in secondary inflorescence stem biomass of 49% to 75% compared to wild-type plants Arabidopsis thaliana
repression of (ATRAPTOR1B, RAPTOR1, RAPTOR1B, AT3G08850) results in significantly reduced and delayed growth Arabidopsis thaliana
Manganese (Mn) deficiency significantly reduces shoot and root biomass Arabidopsis thaliana
growth rates at the end of the night will be lower in 6:18 conditions than in 12:12 conditions Arabidopsis thaliana
plant height of osgrf6 mutant was decreased compared with wild-type Dongjin (DJ) Oryza sativa
enhanced (TOR, AT1G50030) activity in s1c2 might contribute to faster growth of s1c2 compared with sir1-1 Arabidopsis thaliana
5-week-old Arabidopsis rosettes grown under control conditions Arabidopsis thaliana
fixed set point for pot weight neglects increasing weight of plant Setaria
Percival growth chamber provides 16 h light/8 h dark photoperiod Arabidopsis thaliana
VUP1.1 minor splice variant overexpression leads to phenotype indistinguishable from (VUP1, AT3G21710) full-length overexpression Arabidopsis thaliana
(VUP2, AT1G50930) (VUP3, AT3G20557) and (VUP4, AT5G54790) overexpression leads to severely dwarf plants Arabidopsis thaliana
ssisa mutants grew slowly and displayed lower average fresh weight Arabidopsis thaliana
soil moisture regime (treatment) significantly affects shoot biomass Zea mays
growth defects in ohp1-2 mutants were caused by mutation of (OHP, OHP1, PDE335, AT5G02120) Arabidopsis thaliana
large-CN phenotype under P deficiency has 23% greater shoot biomass in field
severe phosphorus (P) deficiency (0 µm) decreases by shoot fresh weight Arabidopsis thaliana
boron (B) deficiency decreases root biomass Arabidopsis thaliana
mutants with reduced carbon availability at night have wild-type growth rates in continuous light but reduced growth rates in day-night cycles Arabidopsis thaliana
ES7 (endosidin 7) is potent inhibitor of plant growth Arabidopsis thaliana
(ANAC072, ANAC72, AtRD26, RD26, AT4G27410) represses growth Arabidopsis thaliana
better P acquisition will result in better plant growth Zea mays
(CKRC2, YUC8, YUCCA8, AT4G28720) and (YUC9, YUCCA9, AT1G04180) overexpression increasing total plant height total plant height Arabidopsis thaliana
myosin XI is key factor in Arabidopsis growth Arabidopsis thaliana
carrot lycopene β-cyclase (DcLCYB1) expression in results in increased biomass Nicotiana tabacum
(ATGRP8, CCR1, GR-RBP8, GRP8, RBGA6, AT4G39260) ProSNBE lines completely overcame total plant biomass penalty of severely dwarfed (ATGRP8, CCR1, GR-RBP8, GRP8, RBGA6, AT4G39260) mutants
remaining glutamate cysteine ligase (GCL) activity in cad2-1 (40% of wild-type level) is sufficient to allow wild-type-like growth under nonstressed conditions
young seedlings (20–30 DAS) and older plants (40–50 DAS) showed no significant differences in leaf growth between (ADT3, PD1, AT2G27820) /4/5/6 and wild-type lines Arabidopsis thaliana
MG-20 plants were somewhat bigger than Gifu plants
mutation of (HTB4, AT5G59910) results in thin stem Arabidopsis thaliana
soil N limitation was identified as the main driver of decreased vascular plant above- and belowground production
rhizosphere metabolic mixture comprising soyasapogenol B, 6-hydroxynicotinic acid, lycorine, shikimic acid, and phosphocreatine enhances growth in maize crops
specific rhizosphere metabolites do not directly regulate plant growth and nutrient uptake
CSS10 dry weight was not increased in CSS lines compared with WT Oryza sativa
plants from both HS and HR treatments had similar areas to control plants Chenopodium quinoa
leaf area did not differ between transgenic and wild-type plants Nicotiana benthamiana
sulfur (S) deficiency reduces shoot and root biomass Arabidopsis thaliana
chlorine (Cl) deficiency does not affect shoot and root biomass Arabidopsis thaliana
(AGL24, AT4G24540) (AGL22, FAQ1, SVP, AT2G22540) (AGL20, ATSOC1, SOC1, AT2G45660) plants are larger than (AGL24, AT4G24540) (AGL22, FAQ1, SVP, AT2G22540) plants Arabidopsis thaliana
cold treatment reduces height of many accessions Brachypodium spp.
overexpression of GmEXPB2 elevates plant biomass Glycine max
mature tobacco plants grown in greenhouse with additional lighting of 100 μmol photons m−2 s−1 for 16 h photoperiod Nicotiana tabacum
growth rates following an unexpected extension of the night are much lower than following a normal night Arabidopsis thaliana
transgenic Arabidopsis plants expressing ShMKS2 or both ShMKS1 and ShMKS2 still had reduced growth rate Arabidopsis thaliana
Fe deficiency causes concomitant reductions in biomass production Arabidopsis thaliana
reduced average nuclear ploidy level causes growth defects of (ATGRP8, CCR1, GR-RBP8, GRP8, RBGA6, AT4G39260) mutants Arabidopsis thaliana
Transgenic plants complemented with (OHP, OHP1, PDE335, AT5G02120) grew normally Arabidopsis thaliana
MS Modified Basal Salt Mixture without Nitrogen was used for plant growth media Arabidopsis thaliana
impaired microtubule organization is associated with reduced plant size Arabidopsis thaliana
plants grown in soil in a greenhouse Arabidopsis thaliana
moderate accumulation of mannitol facilitates increased biomass Triticum aestivum
seedlings of transformed PLA promoter- uidA plants were transferred into 24-well plates filled with liquid 1/2MS + 2% glucose Arabidopsis thaliana
OsMED14_1 knockdown produces pleiotropic effects such as less height Oryza sativa
plants with varying degrees of Arabidopsis (TOR, AT1G50030) (AtTOR) overexpression demonstrate that AtTOR is essential for postembryonic growth Arabidopsis thaliana
tandem affinity tag (TAP)-tagged (PCK2, PEPCK, AT5G65690) restores growth parameters Arabidopsis thaliana
Rca-α only-expressing lines underperformed compared to WT plants and Rca-β only counterparts Arabidopsis thaliana
transgenic expression of cellulase enhanced growth of whole plant bodies Populus trichocarpa
control aspen growth monitored by plant height measurement
plants from all treatments had similar shoot dry weight after 11 days of heat treatment Chenopodium quinoa
shoot dry weight without panicles was significantly affected by shoot heating Chenopodium quinoa
bp er fsh plants are almost twice the height of bp er parent line Arabidopsis thaliana
5-FC became toxic at concentrations of 1 mM or higher Arabidopsis thaliana
5-azacytidine treatment increased growth of rice seedlings Oryza sativa
photosynthesis drives growth in the rest of the tree Picea abies
mir plants had root length reduced by 43% compared to WT plants grown in absence of Fe
TREHALOSE-6-PHOSPHATE (T6P) inhibition of (AKIN10, KIN10, SnRK1, SnRK1α1, SNRK1.1, AT3G01090) signaling occurs in actively growing tissue Arabidopsis thaliana
MIR171c-overexpressing plants manifest altered plant height
total dry weights of CSS16 and CSS10 under ambient CO2 were reduced to 50% and 70% of wild-type respectively Oryza sativa
dry weights of other organs and total dry weight in CSS lines under elevated CO2 were almost recovered to level of wild-type Oryza sativa
seeds were sown directly into soil Arabidopsis thaliana
overexpression of rice PIN5b and other PINs producing dwarf plants Oryza sativa
Mp myosin XI-driven cytoplasmic streaming in 4KO can contribute to plant growth in Arabidopsis Arabidopsis thaliana
toxicity of 5-FC first tested on quartz sand plates supplemented with MS solution
OsCIPK genes overexpression had no negative growth effects in plants Oryza sativa
double knockout mutant ( (ATXT1, AtXXT1, XT1, XXT1, AT3G62720) and (ATXT2, AtXXT2, TXT2, XT2, XXT2, AT4G02500) ) exhibited slow growth Arabidopsis thaliana
irx mutants some are dwarf Arabidopsis thaliana
OsMED14_1 overexpression transgenic rice plants show no obvious differences compared with wild-type plants Oryza sativa
ASK1-containing SCF complexes are important for regulating plant growth Arabidopsis thaliana
Rca-α only lines grew more slowly in various light conditions Arabidopsis thaliana
many seeds failed to germinate for one Nicotiana benthamiana
Arabidopsis thaliana plants grown under 12 hour-12 hour day/night cycle at 21°C and 60% humidity with 100 μmol s−1 m−2 light Arabidopsis thaliana
seeds were transferred to rooms at 22°C Arabidopsis thaliana
nitrogen is major soil nutrient
GFP in excess of 35% TSP is the likely reason for the significantly reduced growth
Spring bread wheat (Triticum aestivum L. cv. Bobwhite) plants grown in 1.5-l pots containing University of California mix Triticum aestivum
NIL HR5 shows increase of 17.3 cm in plant height under long-day conditions
(AtHSPR, SMXL4, AT4G29920) (SMXL5, AT5G57130) shoots supported by wild-type root show fully restored stem diameter and overall growth stem diameter and overall growth Arabidopsis thaliana
phosphorus is major soil nutrient
point c moves away from observer at considerably faster rate
plant length and leaf number in CSS lines were at similar levels to plant length and leaf number in wild-type Oryza sativa
δ13C leaf in the well watered treatment had relatively strong correlations with biomass Setaria
HS plants had similar dry weights to control plants at harvest Chenopodium quinoa
ectopic expression of OsPIP1;3 gene resulted in greater biomass Nicotiana benthamiana
increased total plant assimilation is reflected in higher plant yields under fluctuating light Nicotiana tabacum
most seeds germinated for the last line Nicotiana benthamiana
zaxinone has growth-promoting activity growth promotion Oryza sativa
transgenic plants had greater biomass accumulation with greater fresh and dry weights than wild-type plants Nicotiana benthamiana
(GMD2, MUR1, MUR_1, SFR8, AT3G51160) mutants exhibit dwarf phenotype Arabidopsis thaliana
adoption of bryophytes as production platforms is hindered by slow growth
medium irradiance (MI; 500 μmol quanta m⁻² s⁻¹) plants have higher relative growth rate (RGR) Flaveria bidentis
plants exposed to elevated RZ [CO2] of 50,000 ppm show significantly greater root fresh weight (FW) and dry weight (DW)
tobacco plants transformed with BjCET4 under Cd stress showed significantly enhanced shoot biomass production Nicotiana tabacum
content of Rubisco and catalytic properties contribute to growth phenotype of CSS lines Oryza sativa
GFP-Mp myosin XI-Full expression partially rescues growth defect of 4KO mutant Arabidopsis thaliana
most seeds germinated for the other line Nicotiana benthamiana
low level of OsMAPK6 could impair biomass production of rice Oryza sativa
plants with varying degrees of Arabidopsis (TOR, AT1G50030) (AtTOR) silencing demonstrate that AtTOR is essential for postembryonic growth Arabidopsis thaliana
auxin is major growth-promoting hormone
enhanced expression of most PINs could be one of possible causes for smaller height Oryza sativa
RNAi lines had a reduced above-ground biomass compared with WT when grown under 8 h days Solanum andigena
alterations in protein expression or phosphorylation of Rca-α of rwt46 and DRA46 plants are not cause of slow plant growth in short day conditions Arabidopsis thaliana
plants grown from seeds selected for absence of fluorescence Arabidopsis thaliana
(APO2, emb1629, AT5G57930) mutant included dwarf stem Oryza sativa
xyloglucanase (AaXEG2) overexpression results in faster growth Populus trichocarpa
no significant difference in above-ground biomass was observed for either OE or RNAi transgenic lines under 16 h days OE or RNAi transgenic lines Solanum andigena
Jatropha cell cultures grow under environmental conditions differing from field-grown plants Jatropha curcas
bp er fsh plants are not as tall as L er single-mutant Arabidopsis thaliana
BrLhcb1-silenced (ARK3, AtKINUa, PAK, AT1G12430) choi have lower biomass Brassica rapa subsp. chinensis
35Spro–mSCL6-IV–LUC/35Spro–MIR171c#2 double transgenic plants are significantly shorter than 35Spro–MIR171c#2 plants
CSS10 showed significantly higher tiller numbers at final time points than wild-type under the conditions Oryza sativa
mutants deficient in gibberellins (GAs) display dwarf plant architecture Arabidopsis thaliana; Solanum lycopersicum
root heating had a more pronounced effect than shoot heating on shoot biomass Triticum aestivum
(ASK1, ATSKP1, SKP1, SKP1A, UIP1, AT1G75950) inflorescence stems grew more slowly than WT plants Arabidopsis thaliana
content of Rubisco might be a larger determinant of growth phenotype of CSS lines Oryza sativa
TE-2-6b gene targets conserved plant growth mechanism Arabidopsis thaliana; Nicotiana tabacum
OsPIP1;3 overexpression plants grew better and accumulated more biomass than WT plants Nicotiana tabacum
BrCCA1-silenced (ARK3, AtKINUa, PAK, AT1G12430) choi show reduced fresh weight Brassica rapa subsp. chinensis
only few plants (three out of approximately 150) developed normally Nicotiana benthamiana
tomato has optimal growth temperature of 25°C to 30°C in daytime Solanum lycopersicum
(QRT2, AT3G07970) overexpression lines have reduced plant height Arabidopsis thaliana
Spinach (Spinacia oleracea var. Lina) harvested 2–3 months after sowing Spinacia oleracea
plant area extracted from image data was 59.8% higher in HRS plants than in control plants Chenopodium quinoa
OsMED14_1 RNAi transgenic plants (T1 generation) show slow vegetative growth and achieve lesser height than wild-type counterparts Oryza sativa
disruption of AtAKT2 did not affect plant growth under long-day conditions Arabidopsis thaliana
5-week-old axs1-1 axs2-1/+ mutants showed growth defects resembling (GMD2, MUR1, MUR_1, SFR8, AT3G51160) mutant Arabidopsis thaliana
mutant seeds affected in different core RdDM elements were exposed to optimal growth conditions Arabidopsis thaliana
(AtLEC1, EMB 212, EMB212, LEC1, NF-YB9, AT1G21970) overexpression results in smaller plants Arabidopsis thaliana
plants were grown at 21°C under continuous illumination (50 μmol m−2 s−1) Arabidopsis thaliana
athak5-3 plants show reduced tissue fresh weight at day 60 Arabidopsis thaliana
athak5-3 plants show important statistically significant reduction in tissue fresh weight at day 74 Arabidopsis thaliana
Spinach (Spinacia oleracea var. Lina) grown in hydroponic culture Spinacia oleracea
increased total plant assimilation is reflected in higher plant yields under fully controlled constant light Nicotiana tabacum
plants can be grown under simulated conditions
brassinosteroid and ethylene-insensitive protein 2 (ATEIN2, CKR1, EIN2, ERA3, ORE2, ORE3, PIR2, AT5G03280) regulation by (TOR, AT1G50030) modulates hypocotyl elongation and root meristem activation
TORC can define whether plants should commit to certain growth-related processes
young leaves of dexamethasone (dex)-induced (CYP98A3, REF8, AT2G40890) pOpON showed growth not restored to wild-type level Arabidopsis thaliana
OsNIP3;1 knockout resulted in retarded growth Oryza sativa
Partial removal of (ATGRX4, GRX4, GRXS15, AT3G15660) from mitochondria slowed whole-plant growth and respiration Arabidopsis thaliana
sulfur deficiency treatment does not show correlation with shoot biomass loss Flaveria species
many Zingiberales plants require high levels of humidity Zingiber officinale
four independent T1s tested in parallel using 2 mm 5-FC Nicotiana benthamiana
plant genotypes were grown for 10 weeks under greenhouse conditions Parasponia andersonii
TORC prevails as underlying regulator of growth and developmental processes
mir plants had shoot length reduced by 18.2% compared to WT plants grown in absence of Fe
seedlings of transformed PLA promoter- uidA plants were grown for 12 days Arabidopsis thaliana
Potato (Solanum tuberosum var. Desirée) grown under the same conditions as Pea seedlings (Pisum sativum var. Feltham First) Solanum tuberosum
>20 shoots in axs1-1 axs2-1/+ mutants were able to elongate until maturity with comparably larger stems but smaller than wild-type Col-0 plants Arabidopsis thaliana
elemental growth rate profile provides information about growth of primary plant body
growth arises from intrinsic properties and hierarchical organization of plant system components
rice plants grown under 12 h light, 26°C, 80% relative humidity (RH), followed by 12 h dark, 20°C, 60% RH Oryza sativa
(AtVIP1, SUE3, VIP1, AT1G43700) and (SUE4, AT3G55880) mutants on MS medium containing 1.5 mM sulphate showed similar growth of roots and shoots to wild type Arabidopsis thaliana
plants growing in dry soil causes hampered root growth
biomass production was simulated satisfactorily simulation model Triticum aestivum
relative growth rate was compared between resistant versus susceptible populations Lolium rigidum
(ENT1, ENT1,AT, AT1G70330) mutants exhibit growth restrictions Arabidopsis thaliana
APRI treatment maintained shoot biomass
wild-type BSMV infection does not show obvious reductions in overall plant growth Zingiber officinale
atakt1-2 plants show similar root and shoot fresh weights Arabidopsis thaliana
(AtNPF8.1, ATPTR1, NPF8.1, PTR1, AT3G54140) 5 have function in biomass Arabidopsis thaliana
polar auxin fluxes are required to maintain fundamental processes of development and organogenesis Arabidopsis thaliana
rwt46 and DRA46 plants showed an ~40% reduction in fresh weight Arabidopsis thaliana
OsMAPK6 plays a critical role in biomass production of rice Oryza sativa
Arabidopsis root peak elemental growth rate perfectly matches values obtained for maize and bean roots Arabidopsis; Zea mays; Phaseolus vulgaris
gibberellin synthesis promotes cell elongation
Bean roots are bigger than Arabidopsis roots Phaseolus vulgaris; Arabidopsis
CNGC2-CNGC4 is critical for sustaining growth
debranched+auxin treatment produces approximately half the total number of leaves on primary branches compared to NPA treatment
nitrate availability influences vegetative biomass Arabidopsis thaliana
relative growth rate (RGR) varies markedly among genotype Populus deltoides × P. nigra
white poplar (P. alba L.) expressing VHb did not observe general growth improvements Populus alba
modern wheat had intermediate relative growth rate (RGR), relative growth rate of shoot (RGRs), and relative growth rate of root (RGRr) Triticum aestivum
(SUT1, AT5G63020) mutants have greatly reduced stature Zea mays
targeted mutagenesis of genes involved in immunity and flowering maximises biomass Nicotiana benthamiana
water influx drives cell expansion
double (ATCAD4, CAD, CAD-C, CAD4, AT3G19450) C/ D mutants show normal or almost normal size Arabidopsis thaliana
A-genome cottons show lower shoot growth (SG) under control conditions Gossypium spp.
accumulation of Met is a potential cause of retarded plant and cell culture growth Arabidopsis thaliana
kinematics shows maize and bean roots are bigger than Arabidopsis roots because they have more and bigger cells Zea mays; Phaseolus vulgaris; Arabidopsis
salt stress reduces growth rate
ES20-1 more strongly inhibited plant growth
plants in no-N or 15 μM N treatments produced less biomass Hakea actites
constitutive over-production of salicylic acid (SA) results in dwarfed phenotype Arabidopsis thaliana
tritordeum and Cham maintained their ranking under different stress treatments durum wheat; tritordeum
this study followed up on reports to understand how AHA affects plant growth
cells in region a are not expanding much cell expansion
Bean roots have more and bigger cells Phaseolus vulgaris
auxin regulates various growth processes
(AtPGR5, PGR5, AT2G05620) (CRR2, AT3G46790) double mutant showed severe growth retardation under low-light growth conditions
jasmonic acid (JA) stimulate cell division
GS isozymes are correlated with total biomass
(SAPX, AT4G08390) (TAPX, AT1G77490) (AtPGR5, PGR5, AT2G05620) (CRR2, AT3G46790) quadruple mutant had a similar phenotype to (AtPGR5, PGR5, AT2G05620) (CRR2, AT3G46790) double mutant
Q1;1 and Q2;2 mutants (group 1) grow normally
misregulated expression of several (YUC, YUC1, AT4G32540) genes proved importance of (YUC, YUC1, AT4G32540) genes in expansion of leaf lamina and plant height Oryza sativa
BrLhcb1-overexpression (OX) Arabidopsis show improved growth Arabidopsis thaliana
ali1-1/ali1-1 and ali1-1/ali1-2 mutants significantly decreases tassel branches Zea mays
(ATMAPK3, ATMPK3, MPK3, AT3G45640) /+ mpk6-1/– plants grown under moderate light conditions were slightly smaller than wild-type
ltp5-1 mutant exhibits multibranching at maturity Arabidopsis thaliana
elevated RZ [CO2] treatment increases shoot dry weight (DW)
Fusarium graminearum infection together with Pseudomonas fluorescens (CHA19, CHR19, ETL1, AT2G02090) ( &Fus) on same root half results in 33% lower total plant biomass after 1 week barley
debranched+auxin treatment produces approximately 20-fold greater secondary branch stem length than NPA treatment
plants that had three or five seminal roots cut differed during subsequent days in leaf growth rate and final leaf length barley
axenic conditions result in slower plant growth
Reduction in panicle length and grain yield was not due to reduction in leaf area Sorghum bicolor
growth rates (GRs) of control-treated plants were higher in the second interval relative to the first interval Arabidopsis thaliana
greenhouse conditions were 28°C, 85% relative humidity Parasponia andersonii
water capture is driving force of plant growth
P-limited plants have significantly lower height Pinus pinaster
debranched treatment produces approximately half the increase in primary branch stem length compared to NPA treatment
WT and 116-9 plants show similar growth irrespective of treatments
AtRGP2:GFP transgenic plants have significantly decreased total biomass Nicotiana tabacum
whole-plant biomass reached 39±3 g DW plant −1 at day 35 Brassica napus
Pro-197-Ser mutation exhibits no significant effects on plant growth Lolium rigidum
higher extractable (AHAS, ALS, CSR1, IMR1, TZP5, AT3G48560) activity caused by Trp-574-Leu mutation has no adverse effect on Lolium rigidum vegetative growth Lolium rigidum
Wedelia chinensis exhibits more strongly inhibited total biomass production Wedelia chinensis
over-expression of (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) in CESA mutant backgrounds can make plants larger and enhance leaf petiole elongation but cannot completely rescue dwarf phenotype of CESA mutants Arabidopsis thaliana
eve1-D/+ plants exhibited dwarf phenotype Arabidopsis thaliana
debranched treatment produces approximately half the total number of leaves on primary branches compared to girdled treatment
T-DNA insertion mutant of (BIGYIN, FIS1A, AT3G57090) showed growth inhibition Arabidopsis thaliana
negative DIF treatment reduces biomass Pisum sativum
L-glutamine treatment partially restored normal vegetative growth pattern in BABA-treated Arabidopsis Arabidopsis thaliana
ltp5-1 mutant exhibits dwarfed inflorescence stature Arabidopsis thaliana
girdled treatment produces fewer leaves on main stem than control treatment
plants with no detectable xyloglucan have only relatively subtle changes in growth under standard conditions
culms of OsMED14_1 RNAi plants are narrower than wild-type counterparts Oryza sativa
OsYUC1 downregulation produced dwarf rice plants Oryza sativa
Epigenome engineering could be utilized to develop crops with improved growth rates
cells undergoing diffuse growth include seeds
Tsu-0 exhibited large biomass Arabidopsis thaliana
CO2 enrichment stimulates growth more at warmer temperatures Lactuca sativa
BR-related mutants have not much different dry weight above ground per seedling compared to wild type at early developmental stages Arabidopsis thaliana
Burkholderia phytofirmans PsJN colonization is associated with growth promotion Vitis vinifera
ratio for the control plants was significantly reduced compared with all the transgenic lines Populus trichocarpa
flooding inhibits plant development
multiple loss-of-function receptor mutants grow slowly Arabidopsis thaliana
growth responses may account for differences in overall plant productivity Solanum lycopersicum
young tomato plants grown for 25 d using nutrient film technique Solanum lycopersicum
HKL1-FLAG transgenic line resulting in almost a 2-fold decrease in plant size Arabidopsis thaliana
abscisic acid plays critical roles in numerous physiological processes during plant growth
tissue expansion is loosely co-ordinated with cell division
stress-tolerant progeny resulted in 2.4-fold increase in dry weight Arabidopsis thaliana
growth recovery in spring is fundamental for the survival of conifers in boreal regions Picea abies
plants can be grown in locations spanning the native range limits of a species
ali1-1/ali1-1 and ali1-1/ali1-2 mutants significantly decreases tassel height Zea mays
host plant growth is less responsive to S availability legumes
increased rhizosphere CO2 concentration caused significant increase in biomass accumulation in tomato seedlings Solanum lycopersicum
plants grown under RZ [CO2] of 10,000 ppm show significantly greater root dry weight (DW)
blue light-containing irradiance shows trend to higher biomass production
meta-analysis is extended to range of other environmental factors important for plant growth
enriching rhizosphere dissolved inorganic carbon (DIC) concentration increased biomass of salinized tomato plants Solanum lycopersicum
girdled treatment produces significantly lower primary branch stem length than control treatment