| cold-affiliated species |
show area-based J max_25 is 29% lower (6.52 μmol m−2 s−1 per degree of warming) at |
22°C than 14°C growth site |
|
| catalytic efficiency of Rubisco |
may differ in |
species that have evolved under contrasting thermal regimes |
|
| Rubisco kinetic properties |
may be improved in some species more than others with |
current climatic warming |
|
| Rubisco in Inga species |
may be optimised to |
warmer conditions |
Inga marginata; Inga spectabilis |
| oxygen rates on Day 1 in turbid water column |
varied from |
3.5 up to 6 μmol O2 (μg Chl a)−1 h−1 |
|
| samples on Day 3 |
had lower ETR max values than |
samples on Day 1 |
|
| lower carbon to chlorophyll a ratio (C : Chl a) |
entails |
increase in pigment content per cell |
|
| organisms expressing ID Rubisco |
show |
positive correlation between kcat c and Kc |
|
| Acetabularia acetabulum |
has |
highest catalytic oxygenation efficiency (kcat o : Ko) |
Acetabularia acetabulum |
| CCM effectiveness |
influences |
Rubisco kinetic traits and Rubisco concentration |
|
| higher Arub in analyzed macroalgal species expressing ID Rubisco |
occurs only at |
Cc < 60 μbar |
|
| gp CO2 values |
were similar among |
analyzed chlorophyte and rhodophyte species |
|
| thylakoid membranes |
are site of |
electron transport chain |
|
| accounting for CO2 concentration at the surface of photosynthetic mesophyll cells (cw) |
allows more detailed description of |
CO2 and water vapor gradients within the leaf |
Capsicum annuum; Helianthus annuus; Gossypium hirsutum |
| mesophyll conductance to CO2 (gm) calculation |
relies on |
precision of ci calculations |
|
| patchy stomatal conductance |
might be an indication of |
unusual observations in cw estimates |
|
| delayed springtime photosynthesis resumption (DSPR) |
reduced ecosystem LUE by 30–70% at many site-years during |
spring |
|
| late frost events that occur after leaf unfolding |
can have |
large impact on forest productivity |
|
| high-light or low-temperature conditions |
show contrasting |
PSII excitation pressure |
|
| Cytb6f genes |
are downregulated under |
low-light (24–72 h) and low-temperature (6 h) treatments |
Thalassiosira pseudonana |
| gene expression within the photosynthesis pathway |
contrasts in sign to the response to |
low-light and high-temperature stress |
Thalassiosira pseudonana |
| C3 grasses |
compared with |
species with C4 pathway |
|
| irrigation |
resulted in higher |
needle-level net photosynthesis (A) |
Pinus sylvestris |
| PSI functionality |
is severely affected by |
severe drought stress |
Arabidopsis thaliana |
| red light |
promotes highest photosynthetic efficiency (Fv/Fm) in |
Phaeocystis globosa |
Phaeocystis globosa |
| energy distribution |
alters |
carbon fixation |
|
| mesophyll conductance (gm) |
is associated with |
larger chloroplasts |
|
| FTSZ1-16 line |
shows markedly decreased |
net CO2 assimilation rate |
Nicotiana tabacum |
| FTSZ1-16 line |
shows significantly perturbed |
photosynthetic electron transport rate |
Nicotiana tabacum |
| light absorptance within leaf |
is a function of |
concentration and distribution of absorbing pigments |
|
| FTSZ1-16 line |
did not show stronger phenotype when comparing steady state with dynamic response of |
NPQ to varying light intensities |
Nicotiana tabacum |
| impairment of chloroplast movement |
can make plants more prone to |
photoinhibition |
|
| reduction in chloroplast size |
seemed to have very little impact on |
NPQ under steady-state and fluctuating light |
Nicotiana tabacum |
| ChlF in (CP22, NPQ4, PSBS, AT1G44575) mutant |
increases due to |
reduction of plastoquinone pool in increasing light |
Arabidopsis thaliana |
| antenna excitation |
eventually controls |
ChlF |
|
| Photosystem I (PSI) fluorescence |
decays quickly on |
c. 50 ps timescale |
|
| chloroplast CO2 concentration under atmospheric conditions (CC400) |
is positively correlated with |
total leaf conductance to CO2 under atmospheric conditions (gtot400) |
|
| CO2/O2 specificity factor of Rubisco (SC/O) |
is positively correlated with |
protein content per unit leaf area (PAREA) |
|
| variation in area-based light-saturated photosynthetic rate (Aa) |
was largest |
across years |
Vaccinium angustifolium; Vaccinium myrtilloides |
| water and nitrogen resources |
are considered broadly substitutable in |
photosynthesis |
|
| CO2 supply (proportional to gs) |
contributes to setting |
ci:ca |
|
| enhancing the adaptation of photosynthesis to diverse environmental settings |
is required to |
increase yield |
|
| Brassica nigra |
had significantly higher maximum rate of electron transport than |
Brassica rapa |
Brassica nigra; Brassica rapa |
| Hirschfeldia incana |
had lower |
limitation by total diffusional conductance |
Hirschfeldia incana |
| smaller mesophyll thickness |
led to |
maximum photosynthetic capacity |
|
| photosynthesis |
uses |
carbon dioxide |
|
| increased CO2 levels |
impact |
photosynthetic productivity |
|
| Pt9029 influence on TaRCA function |
leads to |
consequential effects on Rubisco enzyme activity |
Triticum aestivum |
| Fast Assimilation-Temperature Response (FAsTeR) method |
measures |
plant assimilation-temperature response |
|
| young leaves in Cucurbita pepo |
begin fixing carbon when they are only |
8% expanded |
Cucurbita pepo |
| Flaveria sonorensis |
is |
C2 photosynthetic type |
Flaveria sonorensis |
| phycobiliproteins |
include |
phycoerythrin (PE) |
|
| CCMP1630 |
shows |
F v / F m values remained at or near maximal levels at 27°C |
Synechococcus spp. |
| pioneer Inga species |
perform well in |
high light conditions |
|
| Ellisolandia elongata |
shows net photosynthesis completely inhibited under presence of |
EZ (ethoxyzolamide) |
Ellisolandia elongata |
| shorter lived leaves |
have higher |
maximum carboxylation rate of the enzyme Rubisco (Vcmax) |
|
| phytoene boost |
is proposed to interfere with |
photosynthesis |
|
| drop in ɸPSII |
is likely derived from |
transcription-independent downregulation of proteins associated with photosynthetic electron transport |
Nicotiana benthamiana |
| light absorption, excitation energy transfer, and primary photochemistry in photosynthesis |
are |
temperature-independent |
|
| photosynthesis genes |
are similarly expressed under |
all nutrient-starvation treatments, ROS, LT, HL, and LpH |
Thalassiosira pseudonana |
| net photosynthetic rate of Cleistogenes squarrosa |
largely increased |
phosphorus addition |
Cleistogenes squarrosa |
| stomatal closure during summer |
drives |
lower peak photosynthesis and thermal optimum in control trees |
Pinus sylvestris |
| photosynthetic adjustments |
can be beneficial in future as |
temperatures and frequency of heatwaves are predicted to increase |
Pinus sylvestris |
| light-harvesting complex II (LHCII) trimers |
can act as antenna for |
active Photosystem II (PSII) complexes |
Arabidopsis thaliana |
| 14-d water deficiency |
causes drop of approximately 20% in |
F v / F m |
Arabidopsis thaliana |
| (SLG1, AT5G08490) lines |
showed |
wild-type phenotype in terms of photosynthesis |
Solanum lycopersicum |
| FTSZ1-16 line |
shows significant decrease in |
rate of linear electron transport |
Nicotiana tabacum |
| CCM metabolites |
play a central role in |
photosynthesis |
|
| ambient light reduction by 95% |
caused |
lower photosynthetic rates in Posidonia australis |
Posidonia australis |
| ChlF in (CP22, NPQ4, PSBS, AT1G44575) mutant |
decreases when |
plastoquinone pool becomes more oxidized in decreasing light phase |
Arabidopsis thaliana |
| C4 plants |
have enhanced |
water-use efficiency |
|
| photosynthetic rate of lower leaves in a canopy |
is determined more by light than by |
photosynthetic capacity |
|
| linear electron transport (LET) in chloroplasts |
gives |
ATP : NADPH ratio of 1.5 |
|
| corrected αbs value for NAD-ME and PEP-CK subtypes |
remains essentially unaltered |
original αbs values |
|
| stomatal conductance to H2O under atmospheric conditions (gs400) |
is positively correlated with |
maximum rate for carboxylation reaction of Rubisco at 25°C (VCmax,25) |
|
| rate of electron transport through PSII under atmospheric conditions (J400) |
is positively correlated with |
total leaf conductance to CO2 under atmospheric conditions (gtot400) |
|
| Total tree leaf area |
regulates |
photosynthetic leaf area |
|
| delta BL (ΔBL) and delta TR (ΔTR) |
respond to changing |
atmospheric CO2 concentration (Ca) |
|
| (HUP43, PCO2, AT5G39890) limitation |
is counteracted by |
elevational reductions in pO2 and photorespiration |
|
| decrease in fluorescence-derived yield of PSII (Y(II)) |
lowers |
modelled rate of (PAS2, PEP, PEPINO, AT5G10480) carboxylation (VP) |
maize; sorghum |
| CO2 concentration in the intercellular airspaces (Ci) |
has |
elasticity to dehydration |
maize; sorghum |
| absorption spectra analysis |
focused on |
blue–green wavelengths |
Ostreococcus tauri |
| chloroplast coverage in inner BS |
averages |
2.4% in typical C3 species |
Helianthus annuus; Senecio flaveriae; Flaveria cronquistii |
| electron transport chain (ETC) |
includes |
PSII |
|
| phycobilins |
extend |
range of photosynthetically active radiation the cell can use beyond that of chlorophyll |
|
| oxidized PQ pool |
causes PBS to become associated with |
PSII (state 1) |
|
| Synechococcus spp. |
is |
in cyanobacteria, including Synechococcus spp., the main light-harvesting antennae are water-soluble pigment-protein complexes called phycobilisomes |
|
| PBS-related proteins |
showed |
more variable responses |
Synechococcus sp. WH8102 |
| oxygen production |
is |
photosynthetic target |
|
| phytoplankton exposed to rapid unpredictable alterations in multiple global-change drivers |
can regulate |
interplay between energetic supply and demand |
|
| ochrophyte Dictyota fasciola |
has |
lowest gp CO2 value |
Dictyota fasciola |
| subtraction of internal airspace resistance |
would obtain |
more accurate estimate of chloroplast-based traits |
|
| ΔcMix estimates in Helianthus annuus |
ranged between |
−2 and 5 μmol mol−1 |
Helianthus annuus |
| adaxial and abaxial stomatal conductances in Gossypium hirsutum |
did not change greatly during |
light response experiment |
Gossypium hirsutum |
| Δcw for experiments varying atmospheric CO2 concentration (ca), air saturation deficit (ASD), and photosynthetically active radiation (PAR) |
was presented in |
Fig. 5 |
|
| (HTB4, AT5G59910) mutant leaves |
shows decreased |
chlorophyll content |
Arabidopsis thaliana |
| low-temperature and high-light conditions |
can cause |
over-supply of energy from light absorption |
|
| elevated CO2 |
accelerates |
carboxylation by ribulose-1:5-bisphosphate carboxylase/oxygenase |
|
| elevated CO2 |
competitively inhibits |
oxygenation reaction |
|
| A opt |
is usually optimised under |
maximum daytime temperatures |
|
| Pinus sylvestris |
shows low plasticity in |
thermotolerance metrics in response to soil moisture changes |
Pinus sylvestris |
| thermotolerance |
did not change between |
treatments |
Pinus sylvestris |
| high light illumination |
can cause |
photoreduction of oxygen (O 2) |
|
| Drought group |
has higher NPQ values than |
Water group in low actinic light |
Arabidopsis thaliana |
| stomatal conductance (gs) |
has sensitivity coefficient of |
0.06 in Year 1, 0.05 in Year 3, 0.05 in Year 6 |
Agave tequilana |
| simulated water-use efficiency (WUE) |
showed relatively little sensitivity to |
LAI |
Agave tequilana |
| model |
could be used to contrast water saving by CAM plants with |
typical C3 plants |
|
| theoretical maximum εt of Agave spp. (NADP-ME CAM) |
is similar to |
theoretical maximum εt of C3 photosynthesis |
|
| phototrophs |
have developed |
specific light-harvesting pigments |
|
| fucoxanthin |
functions as |
antenna pigment carotenoid in light-harvesting complexes |
|
| pTRV-SlMPK2 plants |
show decreased |
maximal photochemical efficiency of photosystem II (Fv/Fm) |
Solanum lycopersicum |
| proposed effect of thylakoid remodeling on photosynthetic dynamics |
needs to be further examined because |
it may entail fundamental consequences for studies based on dark-to-light transitions |
|
| leaf lifespan (LLS) |
is negatively correlated with |
maximum rate for carboxylation reaction of Rubisco at 25°C (VCmax,25) |
|
| rainfall |
was associated and positively related to |
leaf photosynthetic traits (Aa, Am, AP, AN, gs) |
Vaccinium angustifolium; Vaccinium myrtilloides |
| light-saturated photosynthetic rates |
represented |
expected range for unstressed sclerophyll vegetation in this region |
|
| leaf nitrogen content per area |
boosted |
Rubisco carboxylation |
Hirschfeldia incana |
| photosynthesis in Brassica nigra |
was relatively limited more by |
CO2 diffusion |
Brassica nigra |
| limited RuBP regeneration under light-limiting photosynthesis |
likely due to |
CO2 assimilation decreased slightly in response to temperature elevation |
Arabidopsis thaliana |
| inhibition of Rubisco activase (TaRCA) function |
leads to |
decrease in Rubisco enzyme activity |
Triticum aestivum |
| (ATHSF3, ATHSFA1B, HSF3, HSFA1B, AT5G16820) |
is implicated in |
Chl c and other carotenes synthesis |
Phaeodactylum tricornutum |
| FAsTeR method |
accurately reproduces |
AT response parameters |
|
| genes involved in light reactions of photosynthesis |
are clearly overrepresented in up-regulated genes of |
Rorippa amphibia |
Rorippa amphibia |
| strong induction of genes associated with light-harvesting complexes |
could imply |
presence and/or formation of chloroplasts in belowground tissues |
Rorippa amphibia |
| Helianthus annuus (sunflower) |
is |
C3 photosynthetic type |
Helianthus annuus |
| changes in number and/or size of chloroplasts and mitochondria |
lead to |
greater coverage of BS cell area by organelles in C2 species |
Flaveria angustifolia; Flaveria sonorensis |
| changes in number and/or size of chloroplasts and mitochondria |
lead to |
greater mitochondrial coverage of BS cell area in proto-Kranz species |
Flaveria pringlei; Flaveria robusta |
| BS mitochondria in sunflower, S. flaveriae, and F. cronquistii |
are scattered and often have |
no chloroplast nearby when positioned along cell periphery facing another cell |
Helianthus annuus; Senecio flaveriae; Flaveria cronquistii |
| common intercept of A/Ci responses |
allows for |
approximate C* estimate |
Flaveria robusta; Flaveria angustifolia; Flaveria sonorensis |
| photosynthetic organisms |
are commonly able to perform photosynthesis efficiently over |
a range of temperatures bracketing the optimal growth temperature |
|
| inhibition of chloroplast gene expression |
leads to |
impairment of photosynthesis |
Arabidopsis thaliana |
| rate of ribulose bisphosphate regeneration (J) |
may be limited by |
electron transport rate |
|
| HCO3− transport regulation proportional to light levels or inversely proportional to stromal [HCO3−] |
would increase |
efficiency in light-limited conditions |
|
| C assimilation values after acclimation period |
were slightly higher for |
Day 1 values |
|
| decreased carbon assimilation |
resulted in |
reduced photosynthetic efficiency |
|
| increase in pigment content per cell |
increases |
number of reaction centers available |
|
| analyzed macroalgal species expressing ID Rubisco |
presented higher |
Arub than model C3 terrestrial plant Triticum aestivum |
|
| phytoene build-up |
might cause |
higher rate of D1 degradation |
Nicotiana benthamiana |
| adaxial and abaxial estimated intercellular CO2 concentrations (ci) |
differ by usually larger than |
CO2 concentration at the surface of photosynthetic mesophyll cells (cw) |
Capsicum annuum; Helianthus annuus; Gossypium hirsutum |
| varying the rate of change of photosynthetic uptake with x (m) |
does not significantly affect |
estimation of cw |
|
| GO:0009773 (photosynthetic electron transport in photosystem I) |
was enriched in |
SOM6 |
Setaria viridis |
| Leymus chinensis |
is |
C3 grass species |
Leymus chinensis |
| temperatures exceeding species-specific thresholds |
might negatively impact |
carbon gain |
|
| photosynthetic apparatus and onset of light-dependent photosynthetic electron transport |
modulated as response to |
high light acclimation |
Chlamydomonas reinhardtii |
| drought treatment |
causes appearance of |
long component in time-resolved data |
Arabidopsis thaliana |
| decrease in Photosystem II (PSII) : Photosystem I (PSI) ratio at protein level |
does not correspond to |
decrease at functional level |
Arabidopsis thaliana |
| color phenotype of young leaves |
correlated with |
photosynthetic pigment (carotenoids and chlorophylls) content |
Solanum lycopersicum |
| maximum energy absorption by photosystems |
is |
37.2% |
|
| photorespiration cost in Phase IV |
is considered to be the same as |
photorespiration cost in C3 plants |
|
| photosynthetic activity in P. globosa |
was promoted in |
red light |
Phaeocystis globosa |
| three steps of the Calvin cycle |
require |
ATP |
|
| photosynthetic inefficiencies in large-chloroplast line |
had little effect on |
biomass production when plants grown in well-watered and well-fertilized field conditions |
Nicotiana tabacum |
| NPQ limitations in (AVDE1, NPQ1, AT1G08550) mutant |
have only minor effect on |
redox state dynamics of PSI primary donor P700 |
Arabidopsis thaliana |
| hypothesis and results |
partially explain |
variations in observed quantum yield of CO2 assimilation |
|
| bundle-sheath conductance (gbs) in PEP-CK subtype |
had average value of |
5.0 mmol m−2 s−1 bar−1 |
|
| positive correlation between Mi/BS and gbs |
was not |
significant statistically |
|
| drought |
reduces |
photosynthetic activity |
|
| sucrose and other sugars |
are decreased in |
leaves and axillary buds of dtn1 mutant |
Oryza sativa |
| stomatal conductance to H2O under atmospheric conditions (gs400) |
is positively correlated with |
net photosynthetic rate under atmospheric conditions (AN400) |
|
| laminae with higher leaf protein content per area (PAREA) |
had higher |
optimal Rubisco CO2/O2 specificity (SC/O,opt) values |
|
| Rubisco concentration |
was assumed to be |
34% from the total soluble protein within lamina |
|
| relative limitation by mesophyll conductance and stomatal conductance |
was similar in |
high-light-grown Arabidopsis thaliana |
Arabidopsis thaliana |
| high-light-grown Brassica rapa |
had smaller |
palisade cell diameter |
Brassica rapa |
| lower liquid phase diffusion resistance in Brassica rapa |
due to |
greater Sm,a and Sc |
Brassica rapa |
| increase in leaf temperature |
directly stimulates |
photosynthetic biochemistry |
Arabidopsis thaliana |
| branch hydraulic traits |
might influence |
photosynthetic rates |
|
| light |
has fundamental role in |
photosynthesis |
|
| absorption spectra analysis |
differentiated between |
PSI and PSII |
Ostreococcus tauri |
| BS mitochondria in sunflower, S. flaveriae, and F. cronquistii |
are close to |
chloroplasts when positioned along cell periphery facing IAS |
Helianthus annuus; Senecio flaveriae; Flaveria cronquistii |
| fluorescence traces |
were used to derive |
photosynthetic parameters |
Synechococcus spp. |
| cold-affiliated species |
have highest |
net photosynthetic rate (A net) |
|
| V cmax_25 and J max_25 in warm-affiliated species |
were higher at warm temperatures in |
warm-affiliated counterparts |
|
| mixing and nutrients combined effect |
showed similar response as |
mixing as a single factor |
|
| knowledge of canopy structure and light dynamics |
should improve capacity to |
understand light use efficiency in shade |
|
| calcifying species |
show trend for lower inhibition of photosynthesis at pH 9 relative to |
noncalcifying species within same phylogenetic group |
|
| inverse relationship between carbon concentrating mechanism (CCM) effectiveness (Kc air : Km in vivo ratio) and Rubisco carboxylation efficiency (kcat c : Kc air) |
was found across |
all analyzed macroalgal species |
|
| low Rubisco carboxylation efficiency in species with effective carbon concentrating mechanisms (CCMs) |
evolved differently across |
analyzed macroalgal species |
|
| macroalgae expressing ID Rubisco |
show lower Rubisco carboxylation efficiency derived solely by |
strongly impaired Rubisco CO2 affinity in Ectocarpus elongata relative to other macroalgae |
|
| analyzed seaweeds |
might present |
similar carboxylation potential |
|
| photosynthesis |
harnesses light to build |
chemical bonds |
|
| estimated cw in Gossypium hirsutum light response |
was below |
estimated adaxial and abaxial ci |
Gossypium hirsutum |
| leaves |
have |
a crucial role in resource acquisition via photosynthesis |
|
| PSII photochemical efficiency |
reached a minimum in |
late winter |
|
| thermotolerance |
is often assessed by measuring |
temperature causing a 50% reduction of the maximum quantum yield of the photosystem II (T 50) |
|
| incident light (PPFD) |
had strong relationship with |
net photosynthesis (A) |
Pinus sylvestris |
| photosynthesis and plant productivity |
have not widely been characterised under |
elevated nocturnal temperatures |
|
| εt of Agave tequilana over whole growth cycle (0.021%) |
is much lower than |
theoretical maximum value of C3 or C4 plants |
Agave tequilana |
| three steps of the Calvin cycle |
are regulated by |
specific enzymes |
|
| tobacco (Nicotiana tabacum) lines with contrasting chloroplast sizes |
were used to assess |
photosynthetic performance under steady-state and fluctuating light |
Nicotiana tabacum |
| FTSZ1-16 line |
has reduced |
mesophyll conductance (gm) under ambient oxygen |
Nicotiana tabacum |
| low-chlorophyll soybean mutants |
show leaf-level photosynthesis affected only when chlorophyll content decreased by |
> 50% |
Glycine max |
| eddy covariance (EC) measurement approach |
produced similar estimates for |
photosynthesis (gross primary production, (GPP, VTC4, AT3G02870) ) |
Pinus sylvestris |
| plastocyanin |
was measured in |
oscillating light of various frequencies |
Arabidopsis thaliana |
| stationary component of ChlF yield in wild-type |
is quenched in |
wild-type plants compared to (AVDE1, NPQ1, AT1G08550) mutant |
Arabidopsis thaliana |
| DTN1 loss of function |
influences |
photosynthetic rate |
Oryza sativa |
| mutations in Mp GLK |
impair |
photosynthetic pigment accumulation |
Marchantia polymorpha |
| GLKs |
induce expression of |
PhANGs (photosynthesis-associated nuclear genes) |
|
| leaf lifespan (LLS) |
is negatively correlated with |
relative limitation on AN from photosynthetic capacity (lb400) |
|
| plant species with lower leaf protein content per area (PAREA) and higher total leaf conductance (gtot400) |
had narrower suboptimal |
Rubisco CO2/O2 specificity (SC/O) values |
|
| higher Narea (or Vcmax) |
leads to |
reduced need for water |
|
| Brassica nigra |
had significantly higher |
relative limitation by biochemical capacity |
Brassica nigra |
| species with higher leaf area relative to sapwood area |
had |
higher ci:ca values |
|
| CO2 concentration in the mesophyll (CM) |
has |
elasticity to dehydration |
maize; sorghum |
| sucrose (Suc) |
is |
main product of photosynthesis |
higher plants |
| Tobacco (Nicotiana tabacum) plants with constitutively elevated levels of Tre6P |
were reported to have |
higher rates of photosynthesis per unit leaf area than wild-type plants |
Nicotiana tabacum |
| aerenchymatous species including rice |
form |
functional chloroplasts in roots after prolonged illumination |
Oryza sativa; Rorippa amphibia; Rorippa sylvestris |
| lower CO2 compensation point of photosynthesis in Flaveria pringlei and Flaveria robusta |
indicates |
increase in photosynthetic efficiency |
Flaveria pringlei; Flaveria robusta |
| high light treatment at 1,580 μmol quanta m –2 s –1 |
closed |
many PSII reaction centers |
Synechococcus spp. |
| chloroplast |
is directly associated with |
light absorption |
|
| cold-affiliated species |
show few changes in |
J max_25 and J max_Tg when expressed on mass, N and P bases |
|
| photosynthetically more efficient community |
does not revert |
decreasing trend in carbon fixation with increased mixing speed |
|
| NCP rates on Day 3 |
were lower as compared to |
NCP rates on Day 1 |
|
| diversion of protons and electrons produced at PSII away from carbon fixation |
is due to |
upregulation of alternative electron pathways |
|
| FLL5A locus |
would allow investigation of |
morphological and physiological aspects of photosynthesis |
|
| Miconia borealis |
has |
saturating irradiance 50% higher than other five species |
Miconia borealis |
| cytochrome b6-f complex subunit (PETC, PGR1, AT4G03280) |
showed even earlier decrease |
compared to (PSBA, ATCG00020) and PsaD |
Nicotiana benthamiana |
| Helianthus annuus leaf |
showed nonzero Δci evident only under |
(AATP1, ASD, AT5G40010) equal to, or ≥1.5 kPa |
Helianthus annuus |
| Fe deficiency in (HTB4, AT5G59910) mutant |
might compromise |
chlorophyll synthesis |
Arabidopsis thaliana |
| chloroplast-encoded photosynthesis genes (including the PSI and PSII core, ATP synthase) |
tend to be downregulated under |
low-light |
Thalassiosira pseudonana |
| one year of extreme drought |
caused significant reductions in |
photosynthetic capacity |
Pinus edulis |
| PSII thermotolerance |
may stem from its absence of plasticity compared with |
net photosynthesis and stomatal conductance (gs) |
Pinus sylvestris |
| photosynthetic process |
has crucial role in |
maintenance of homeostasis of different ions across thylakoid membranes |
Chlamydomonas reinhardtii |
| light-harvesting complex II (LHCII) degradation |
occurs at slower rate than |
degradation of all other components of the photosynthetic apparatus |
Arabidopsis thaliana |
| actual light interception, biochemical and anatomical limitations |
reduced theoretical maximum energy conversion efficiency to |
0.0069 actual energy conversion efficiency |
Agave tequilana |
| phenomenological linkage between atmospheric or intercellular CO2 concentrations and stomatal conductance |
has been demonstrated in |
C4 plants |
|
| phenomenological linkage between atmospheric or intercellular CO2 concentrations and stomatal conductance |
has been demonstrated in |
CAM plants |
|
| Talinum triangulare |
is |
facultative CAM plant |
Talinum triangulare |
| many chlorophyll (Chl)-deficient mutants |
display |
altered photosystem I (PSI) / photosystem II (PSII) stoichiometry |
|
| chloroplast size |
could affect |
CO2 conductance from intercellular airspace to chloroplast stroma |
|
| FTSZ1-16 line |
shows significant decrease in |
rate of triose phosphate utilization |
Nicotiana tabacum |
| manipulations of chloroplast size |
are unlikely to achieve |
higher photosynthetic efficiency |
Nicotiana tabacum |
| observed increase in gross primary productivity (GPP) |
but not |
leaf-scale photosynthesis |
|
| eddy covariance (EC) estimates of photosynthesis or gross primary production (GPP) |
are estimated by fitting |
net ecosystem exchange (NEE) to a light response curve |
|
| Arabidopsis thaliana plants |
possess |
two CET pathways |
Arabidopsis thaliana |
| changing stomata conductance |
could be alternative explanation for |
observed slow changes |
|
| parameters estimated from second round |
had values very similar to |
parameters from first round |
|
| leaf total NSC concentration |
is not related to |
leaf gas exchange variables |
Betula pendula |
| total leaf conductance to CO2 under atmospheric conditions (gtot400) |
is positively correlated with |
maximum rate for carboxylation reaction of Rubisco at 25°C (VCmax,25) |
|
| protein content per unit leaf area (PAREA) |
increases |
optimum value of SC/O that maximized AN400 (SC/O,opt) |
|
| field-obtained SC/O values |
were nearly optimal for achieving |
maximum photosynthesis |
|
| high Rubisco CO2/O2 specificity (SC/O) |
decreases |
catalytic rate constant for carboxylation (kcat,C) |
|
| mesophyll conductance from combined gas exchange and chlorophyll fluorescence |
correlated weakly with |
mesophyll porosity |
Arabidopsis thaliana; Brassica nigra; Brassica rapa; Hirschfeldia incana |
| mesophyll thickness |
had substantial contribution to |
anatomically explained variability in mesophyll conductance between high-light and low-light plants |
Arabidopsis thaliana; Brassica nigra; Brassica rapa; Hirschfeldia incana |
| simulations of photosynthetic response to temperature |
show that |
fixed, empirical b' values (e.g. 27 per mille) cannot explain changes in photosynthetic discrimination caused by temperature and accompanying variation in photorespiration |
|
| angiosperms |
compared to gymnosperms, have greater |
photosynthetic rates |
|
| chloroplast-to-nucleus retrograde signaling |
is essential for |
efficient function and assembly of photosynthetic apparatus |
|
| FAsTeR method |
is |
method for measuring acute temperature response of photosynthesis |
|
| temperature |
is a major factor that controls |
photosynthetic rates |
|
| photosynthesis |
serves as |
main energy source for autotrophic organisms |
|
| why1why3polIb-1 mutant line |
reduces |
plant photosynthetic capacity |
Arabidopsis thaliana |
| CIP treatment |
reduces |
plant photosynthetic capacity |
Arabidopsis thaliana |
| total chlorophyll level in wild-type plants |
was |
2.19 ± 0.06 mg g−1 fresh weight |
Arabidopsis thaliana |
| improved Rubisco kinetic properties |
may grant |
greater affinity for CO2 and increased rates of carbon fixation |
|
| Enriched samples on Day 1 |
had tendency of lower C assimilation than |
Ambient samples |
|
| rhodophyte Ellisolandia elongata |
has |
lowest maximum net photosynthetic rate (An max) |
Ellisolandia elongata |
| cellular characteristics of wheat |
should help maintain |
high photosynthetic carbon assimilation irrespective of which leaf surface faces the sun |
|
| OsEPF1oeS plants grown in fresh water |
have Photosystem II efficiency (ΦPSII) significantly lower than |
IR-64 |
Oryza sativa |
| MpCRY |
is involved in |
carbon fixation |
Marchantia polymorpha |
| photochemical reflectance index (PRI) |
provides optical indicator of |
photoprotection |
|
| Helianthus annuus in Fig. 3 |
presented |
a value of A lower than the one expected from the A / c w measured under low VPD |
Helianthus annuus |
| modifications of plant architecture |
can regulate |
photosynthesis |
Oryza sativa |
| delayed springtime photosynthesis resumption (DSPR) |
occurs across |
multiple forest sites |
|
| red algae |
possess |
highly efficient photosynthetic capacity |
|
| studies measuring tree thermotolerance responses to drought in situ |
are severely lacking but are needed to |
increase accuracy of predictions in mature managed and natural forests |
Pinus sylvestris |
| high light acclimation |
minimize |
harmful effects of excessive irradiance |
Chlamydomonas reinhardtii |
| drought treatment |
causes increase in |
functional Photosystem II (PSII) : Photosystem I (PSI) ratio |
Arabidopsis thaliana |
| photosynthetic efficiency |
could be improved by |
modifying chloroplast size |
|
| FTSZ1-16 line |
shows 43% lower |
maximum rate of linear electron transport |
Nicotiana tabacum |
| lower net CO2 assimilation in FTSZ1-16 |
could have resulted directly in |
decline in productivity |
Nicotiana tabacum |
| photosystem I components |
dynamics are formed in slow light oscillations partially by |
thylakoid remodeling |
Arabidopsis thaliana |
| oscillatory ChlF signal |
contains |
upper harmonics |
Arabidopsis thaliana |
| pgrl1ab mutant |
shows qualitatively different frequency responses in which |
P700 redox state is largely independent of oscillating light |
Arabidopsis thaliana |
| gas mixture of 1000 μmol mol−1 CO2 with 2% O2 |
was assumed to represent |
nonphotorespiratory condition |
|
| larger leaves |
may increase |
light interception |
|
| CO2/O2 specificity factor of Rubisco (SC/O) |
is negatively correlated with |
mesophyll conductance to CO2 under atmospheric conditions (gm400) |
|
| CO2/O2 specificity factor of Rubisco (SC/O) |
is positively correlated with |
leaf lifespan (LLS) |
|
| CO2/O2 specificity factor of Rubisco (SC/O) |
is negatively correlated with |
total leaf conductance to CO2 under atmospheric conditions (gtot400) |
|
| alien species |
had |
high maximum carboxylation rate at 25°C (VCmax,25) |
|
| relationship between Am and (CHLM, AT4G25080) |
was found only in |
vegetative year 2019 across genotypes of both species |
Vaccinium angustifolium; Vaccinium myrtilloides |
| low-light-grown Hirschfeldia incana |
had greater net photosynthesis per leaf area than |
low-light-grown Arabidopsis thaliana |
Hirschfeldia incana; Arabidopsis thaliana |
| limitation by total diffusional conductance |
was dominant in |
low-light-grown Arabidopsis thaliana |
Arabidopsis thaliana |
| limitation by total diffusional conductance |
was not dominant in |
high-light-grown Brassica rapa |
Brassica rapa |
| PH02Gene20741 (PGR3, AT4G31850) homologous genes from UV sample |
are associated with |
photosynthesis |
Phyllostachys edulis |
| specific excitation of Lhcp with green light |
induced |
phosphorylation of Lhcp |
Ostreococcus tauri |
| sorbitol and sucrose |
are produced by |
leaf photosynthesis |
|
| low light level used in this experiment |
likely contributed to |
seedlings' carbon limitation |
Cucumis sativus |
| cucumber seedlings |
are carbon limited when grown under |
high light |
Cucumis sativus |
| reduction of mesophyll (M) tissue |
could have |
photosynthetic cost |
plants |
| (CPD45, FHY3, AT3G22170) and (FAR1, AT5G22500) |
are required for regulating |
chlorophyll biosynthesis |
|
| PSI (Photosystem I) |
produces superoxide by photoreduction of |
oxygen |
|
| photosynthetic efficiency |
occurs over |
broader range of temperatures than high cell division rates |
Synechococcus spp. |
| total chlorophyll level in tpTOC75-2 |
was |
2.10 ± 0.19 mg g−1 fresh weight |
Arabidopsis thaliana |
| A net, V cmax_25 and J max_25 responses to growth temperature |
agree with |
hypothesis H1 |
|
| NCP : C assimilation ratio |
on Day 3 was lower than on |
day 1 |
|
| mixing as a single factor |
was significant for |
NCP |
|
| ratio Rdark25 : Vcmax25 |
changes vertically |
canopy position |
|
| CO2 assimilation |
is sustained for several seconds postillumination due to |
residual photosynthetic metabolic pools |
|
| CO2 liberated from CaCO3 formation |
can be used as |
source for photosynthesis |
|
| distinct relationship between CO2 and O2 affinities |
was detected for |
ID and IB Rubisco forms in algae |
|
| isolated location of calcifying regions |
would hinder |
diffusion of CO2 generated in calcification toward Rubisco active sites |
|
| overaccumulation of phytoene |
triggers |
decline in photosystem II quantum yield (ΦPSII) |
|
| SbWRKY50-OE sorghum |
show higher expression of |
SbRBCSA |
Sorghum bicolor |
| proximal sampling methods involving collecting leaf samples |
alters |
other factors influencing photosynthesis |
|
| surfaces with higher stomatal density and conductance |
presented |
greatest gradient between adaxial/abaxial ci and cw |
|
| photosynthesis associated nuclear genes (PhANGs) |
include |
genes encoding subunits of photosystem II (PSII) |
|
| rate of respiratory CO2 release in the dark (Rdark, μmol m-2 s-1) |
is among the parameters necessary to estimate |
photosynthetic assimilation (A) |
|
| drought stress |
affects at different stages |
photosystems |
Arabidopsis thaliana |
| stomatal conductance (gs) |
has default value of |
0.1 mol m-2 s-1 |
Agave tequilana |
| photosynthesis (YII) in Phaeocystis globosa |
accounts for |
over 50% of absorbed light energy during exponential growth |
Phaeocystis globosa |
| tricarboxylic acid reduction in red light |
exhibited high regeneration via |
BPGA → GAP step (high expression of GAPDH) |
Phaeocystis globosa |
| enlarged chloroplasts in Arabidopsis and tobacco |
reported to show |
unusually strong midday depression of Φ PSII |
Arabidopsis thaliana; Nicotiana tabacum |
| SlBBX17-overexpression plants |
display increased |
maximal photochemical efficiency of photosystem II (Fv/Fm) |
Solanum lycopersicum |
| pgrl1ab mutant |
lacks |
( (AtPGR5, PGR5, AT2G05620) /PGRL1)-dependent pathway |
Arabidopsis thaliana |
| simultaneous measurements of multiple system variables |
required for understanding |
dynamics in complex systems like plants photosynthetic system |
Arabidopsis thaliana |
| variations of ChlF yield in pgrl1ab mutant exposed to long-period light oscillations |
are stronger than in |
short-period oscillations |
Arabidopsis thaliana |
| work |
anticipate new insights will be gained regarding |
acclimation of these processes to fluctuating light environments |
|
| fraction of Photosystem II (PSII) in bundle-sheath (BS) cells (αbs) in NAD-ME subtype |
ranged from |
0.20–0.38 |
|
| significantly decreased iron contents in leaves |
was not accompanied by |
frequently coinciding decrease in chlorophyll content |
Populus trichocarpa |
| hexoses |
are |
soluble sugars tightly associated with leaf photosynthetic functions |
|
| dtn1-3 mutant |
shows significantly decreased |
net photosynthetic rate (Pn) |
Oryza sativa |
| nine out of 13 lines |
show |
significantly higher Chl and carotenoid content |
Marchantia polymorpha |
| combined morphological and molecular analysis |
underscores |
conserved role of MpGLK in regulating expression of PhANGs |
Marchantia polymorpha |
| leaf dry mass per unit leaf area (LMA) |
is negatively correlated with |
relative limitation on AN from photosynthetic capacity (lb400) |
|
| CO2/O2 specificity factor of Rubisco (SC/O) |
is positively correlated with |
protein content per unit leaf area (PAREA) |
|
| nitrogen content per unit leaf area (NAREA) |
is negatively correlated with |
stomatal conductance to H2O under atmospheric conditions (gs400) |
|
| maximum carboxylation rate (Vcmax) |
decreases proportionally with |
catalytic rate constant for carboxylation (kcat,C) |
|
| stomatal conductance to CO2 |
was lower under low light than under high light for all species except |
high-light-grown Brassica nigra |
Arabidopsis thaliana; Brassica nigra; Brassica rapa; Hirschfeldia incana |
| triose phosphate utilization limitation |
was associated with |
decline in net photosynthesis |
Hirschfeldia incana; Brassica rapa |
| nonequilibrium gas exchange techniques |
have been successfully applied to |
certain other types of photosynthesis measurements |
|
| short-term rise in Tre6P |
could affect |
photosynthetic capacity |
Arabidopsis thaliana |
| stomatal pores |
form |
primary route for CO2 entry for photosynthesis |
|
| phycobilisome (PBS) |
likely associates with reaction centers by |
weak interactions with lipid head groups |
|
| photosynthetic efficiency (Φ PSII) |
was assessed over |
range of irradiances at each growth temperature |
Synechococcus spp. |
| results from this study and Dusenge et al. (2021) |
find no change in |
J max_25 : V cmax_25 with increased growth temperature |
|
| increasing DOM concentrations combined with vertical mixing-mediated light fluctuations |
impair |
photosynthesis of monospecific cultures of cyanobacteria |
|
| oxygen rates on Day 1 |
were significantly higher in turbid water column (kd of 3 m−1) than in clear water column (kd of 0.8 m−1) |
water column attenuation conditions |
|
| Enriched samples on Day 3 |
had significantly higher C assimilation than Ambient ones in turbid water column |
turbid water column |
|
| decrease in maximum carboxylation rate from top-of-canopy to ground |
was less than |
TBM assumptions |
|
| Acetabularia acetabulum |
shows |
highest Arub among macroalgal species |
Acetabularia acetabulum |
| green macroalgal Rubiscos |
show lower |
Ko : Kc ratios (32–40) |
|
| carotenoids, chromanols, and quinones in thylakoid membranes |
participate in |
photosynthesis-related processes |
|
| CO2 concentrations surrounding the mesophyll cells |
must be roughly similar, except for |
few cells next to the stomatal cavity |
|
| additional measurements on selected forest EC sites |
are suggested for |
discriminating effects of protective vs damage |
|
| seasonal modification of the Vcmax parameter |
affects |
rates of A |
|
| irrigated trees |
have significantly higher optimal temperature (T opt) than |
control trees |
|
| thermotolerance |
is usually higher in |
coniferous and evergreen than in deciduous species |
Pinus sylvestris |
| CO2 influx |
limits |
photosynthesis yield |
|
| mesophyll conductance (gm) |
has default value of |
0.1 mol m-2 s-1 |
Agave tequilana |
| realized εt of rice |
is |
approximately 0.02 |
Oryza sativa |
| blue light |
promotes quantum yield (YII) in |
Phaeocystis globosa |
Phaeocystis globosa |
| light energy |
is converted to |
chemical energy |
|
| synthesis of carbohydrates or lipids in the Calvin cycle of P. globosa |
may be related to |
synthesis of GAP and Ru5P |
Phaeocystis globosa |
| upgraded GAPDH (gene and enzyme) in red light |
resulting in |
high production of three- and five-carbon sugars (GAP and Ru5P) |
Phaeocystis globosa |
| increased NPQ at lower light levels in FTSZ1-16 |
was also found in absence of |
blue light |
Nicotiana tabacum |
| sucrose |
is |
major product of photosynthesis in seagrasses |
|
| ChlF yield maximum in α/β boundary |
is found in |
(AVDE1, NPQ1, AT1G08550) mutant |
Arabidopsis thaliana |
| apparent relative Fd-redox states in wild-types |
are hardly changing between |
light minima and light maxima of rapid light oscillations |
Arabidopsis thaliana |
| difference in quantum yield (%) between two gas mixtures |
varied among species from |
4.2% to 23.8% |
|
| fraction of Photosystem II (PSII) in bundle-sheath (BS) cells (αbs) in PEP-CK subtype |
ranged from |
0.36–0.50 |
|
| Chlorella ohadii cultures |
were grown for 24 h in |
low light (LL) or high light (HL) illumination |
Chlorella ohadii |
| PSI |
may undergo |
photoinhibition due to the accumulation of reactive oxygen species (ROS) |
Chlorella ohadii |
| mutant plants after 5-wk hydroponic cultivation |
chlorophyll content of leaves is not considerably altered in |
wild-type (WT) chlorophyll content |
Populus × canescens |
| stomatal conductance |
best explains variation in |
photosynthetic rate |
Betula pendula |
| 17 independent gain-of-function pro35S:Mp GLK-FLAG transgenic lines |
show |
smaller size and greener phenotype in over 80% of lines |
Marchantia polymorpha |
| high-light-grown Brassica rapa |
exceeded net photosynthesis per leaf area of |
high-light-grown Arabidopsis thaliana |
Brassica rapa; Arabidopsis thaliana |
| high-light-grown Brassica rapa |
had significantly higher net photosynthesis on dry mass basis than |
high-light-grown Hirschfeldia incana |
Brassica rapa; Hirschfeldia incana |
| Brassica nigra |
had significantly higher maximum carboxylation rate than |
Hirschfeldia incana |
Brassica nigra; Hirschfeldia incana |
| limitation by total diffusional conductance |
was dominant in |
low-light-grown Brassica nigra |
Brassica nigra |
| high-light-grown Hirschfeldia incana |
had thicker |
cell wall |
Hirschfeldia incana |
| thicker leaves or mesophyll structure with a high surface to volume ratio |
while ensuring |
CO2 diffusion |
|
| high light conditions |
caused |
higher A and J at 28°C |
Arabidopsis thaliana |
| genome size (GS) |
is influenced by |
photosynthetic pathway |
|
| CO2 enrichment |
leads to greater increases in |
(GPP, VTC4, AT3G02870) |
tropical forest plants |
| photosynthesis-related genes ( (LHCB3, LHCB3*1, AT5G54270) and (PSBR, AT1G79040) ) |
are |
potential mediators of higher tolerance in Rorippa species |
Rorippa amphibia; Rorippa sylvestris |
| Flaveria robusta |
is |
C3 species |
Flaveria robusta |
| Flaveria angustifolia and Flaveria sonorensis |
are |
C2 species in the study |
|
| Rd intercept of A/Ci response at 400 µmol m−2 s−1 in F. sonorensis and F. angustifolia |
is shifted to |
lower Ci than estimated C* |
Flaveria sonorensis; Flaveria angustifolia |
| low light |
causes |
convergence of ½ values in C2 and C3 species |
Flaveria species |
| electron transport chain (ETC) |
includes |
PSI |
|
| phycobilisome (PBS) |
can associate with |
PSI or PSII |
|
| state transitions |
balance |
electron flow such that electrons do not accumulate within the ETC |
|
| pulse amplitude-modulated (PAM) fluorometry |
was used to collect |
fluorescence traces |
Synechococcus spp. |
| replacement of C3 crop Rubisco with cyanobacterial Rubisco isoform |
in absence of CCM results in |
decrease in light-saturated CO2 uptake (Asat) |
|
| elevated [CO2] |
causes most Rubisco isoforms to support similar |
light-saturated CO2 uptake (A sat) |
|
| high sensitivity of system to kinetic properties of BicA and BCT1 |
underlines finding that simulated inclusion of HCO3− transporters alone will apparently increase light-saturated CO2 uptake (A sat) |
HCO3− transporters as primary targets for transformation |
|
| maximum rate of photosynthetic electron transport (Jmax_T) |
had |
greatest flux control coefficient (CC) under low light PPFD of 200 μmol m−2 s−1 |
|
| C4 photosynthesis |
differs from |
C3 photosynthesis |
|
| increased SQDG level in the upper leaves of SIR Ri plants |
might be related to |
additional stabilization of PSII |
Solanum lycopersicum |
| understanding of relationship between cell size and photosynthesis |
is still rudimentary and merits |
further research |
|
| LCIA mutation |
has more significant impact on photosynthetic O2 evolution at |
higher pH |
Chlamydomonas reinhardtii |
| LCIB mutants at higher pH |
show reduced O2 evolution rates at |
higher inorganic carbon concentrations |
Chlamydomonas reinhardtii |
| Δ flv4 mutant |
showed approximately 30% smaller |
oxygen evolution rates |
Synechocystis |
| Δ flv4 mutant |
demonstrated a high peak at |
685 nm |
Synechocystis |
| high light intensity or drought stress |
causes singlet oxygen production especially under |
singlet oxygen production |
Synechocystis sp. PCC 6803 |
| flv4-2 operon overexpression |
provides better tolerance to |
photoinhibition |
Synechocystis sp. PCC 6803 |
| Flv2/Flv4-mediated electron transfer mechanism |
is an important electron sink at |
PSII acceptor side |
Synechocystis sp. PCC 6803 |
| Flv2, Sll0218, and Flv4 protein accumulation |
is related to |
presence of functional phycobilisomes |
Synechocystis sp. PCC 6803 |
| coronatine (COR) treatment |
strongly represses |
gene functions associated with photosynthesis |
Arabidopsis thaliana |
| newly developed chlorophyll fluorescence imaging technology |
revealed a previously unreported transient decrease of |
quantum efficiency of PSII (Φ II) at dawn on the morning after coronatine (COR) treatment |
Arabidopsis thaliana |
| overexpression of transcription factors GOLDEN1-like (ATGLK1, GLK1, GPRI1, AT2G20570) or (ATGLK2, GLK2, GPRI2, AT5G44190) |
activates |
photosynthetic gene expression in roots in Arabidopsis lines |
Arabidopsis thaliana |
| rh50-1 mutant |
restores to wild-type-like levels |
(PSAO, AT1G08380) expression |
Arabidopsis thaliana |
| rh50-1 prors1-1 double mutant |
restores |
PhANG expression |
Arabidopsis thaliana |
| SS4N-GS-YFP/YFP-SS4N-GS plants |
had all leaves that were |
green |
Arabidopsis thaliana |
| cyclic electron flow via FDX1 isoform |
may help maintain |
NPQ in FDX2 mutants |
Arabidopsis thaliana |
| Cyt f |
undergoes transcriptional down-regulation by |
Fe deficiency |
Arabidopsis thaliana |
| plant TCA cycle |
likely fulfills role in |
optimization of photosynthesis |
|
| Genes encoding carbonic anhydrases in Haberlea rhodopensis |
are |
repressed during darkness |
Haberlea rhodopensis |
| photosynthesis |
serves as basis for |
biomass accumulation and growth |
Arabidopsis thaliana |
| intraspecific variation in C4 grass |
would be particularly useful in mapping |
traits relevant to improving photosynthesis in crops |
Gynandropsis gynandra |
| reduced levels of polar lipids |
leads to |
reduced photosynthetic capacity |
Arabidopsis thaliana |
| decreased relative chlorophyll a contents in (OHP, OHP1, PDE335, AT5G02120) mutants |
were consistent with |
lack of obvious chlorophyll a-binding PSII core proteins in (OHP, OHP1, PDE335, AT5G02120) mutants |
Arabidopsis thaliana |
| relative amount of PSII in HL |
was drastically decreased in |
Ɗnd4pgrl1 double mutant |
Chlamydomonas reinhardtii |
| LPS |
significantly reduces |
photosynthetic efficiency of PSII in Fv/Fm |
|
| AtBBX21-expressing plants |
have higher rates of |
photosynthesis |
Solanum tuberosum |
| transgenic lines |
have |
higher photosynthetic rates |
Solanum tuberosum |
| 21% O2 condition |
results in |
GOP max of 34.2 μmol m−2 s−1 |
|
| increase in proton motive force across the thylakoid membrane |
down-regulates |
photosystem II activity |
Arabidopsis thaliana |
| light saturation curve measurements |
utilized |
night-adapted (NA) leaves adapted to different light intensities with dark-interval-relaxation kinetics (DIRK) method |
Arabidopsis thaliana |
| Arabidopsis plants with compromised ADT activity |
do not show significantly higher rates of |
carbon fixation |
Arabidopsis thaliana |
| P deficiency treatment |
significantly reduces |
fraction of open reaction centers under steady-state growth light |
Hordeum vulgare |
| electron flow to PSI |
reduces |
inflection at the I-step |
|
| individual leaf darkening (IDL) after 6 days |
decreases |
photosynthetic efficiency |
Arabidopsis thaliana |
| Auxenochlorella protothecoides |
can grow |
autotrophically in light |
Auxenochlorella protothecoides |
| excess light |
cannot be properly absorbed into |
photosynthetic apparatus |
|
| high-light stress in (AVDE1, NPQ1, AT1G08550) lor1 double mutant |
causes |
PSII proteins are degraded and photosynthesis is down-regulated |
Chlamydomonas |
| light transients |
involve |
redox demand fluctuations |
Flaveria |
| reanalysis accounting for competition between CO2 hydration and carboxylation |
would reconcile |
PEPC-derived and Δ18O-derived gm approaches |
Zea mays; Setaria viridis |
| thylakoid membranes obtained through severe mechanical procedures like ultrasonication or passage through French press |
were normally found to be inactive in |
non-cyclic photophosphorylation |
|
| AOX |
plays a significant role in dissipating chloroplastic reducing equivalents in coordination with cyanide-resistant pathway to |
optimize photosynthetic performance |
|
| quenching coefficient qP |
calculated using equation |
qP = [FV(S) – FV]/FV(S) |
|
| Alb3.2 |
interacts with |
reaction center polypeptides of PSI |
Chlamydomonas reinhardtii |
| depletion of Alb3.2 |
shows that Alb3.2 has essential role in assembly of |
PSI (photosystem I) |
Chlamydomonas reinhardtii |
| copper (Cu) |
is cofactor for |
plastocyanin |
Arabidopsis thaliana |
| mixing as a single factor |
was significant for |
(AtETR1, EIN1, ETR, ETR1, RDO3, AT1G66340) max |
|
| maximum net CO2 assimilation rate (A) and stomatal conductance (gsw) |
are simulated at |
09:00 to 10:00 h at top-of-canopy |
|
| Ellisolandia elongata |
has |
highest Rubisco Michaelis–Menten constant for CO2 under ambient O2 (Kc air) |
Ellisolandia elongata |
| Kc air : Km in vivo |
shows negative correlation with |
kcat c : Kc air |
|
| CO2 assimilation rate |
is relevant to |
flag leaf photosynthetic efficiency |
|
| phenological stage and species |
have interactive effects on |
V cmax.25 |
|
| leaf phenology |
has strong effect on |
Vcmax |
|
| aquatic adventitious roots |
develop |
functional chloroplasts |
|
| (LHCB5, AT4G10340) gene |
is upregulated under |
all stressors including low light |
Thalassiosira pseudonana |
| Arctic warming |
stimulates |
primary production |
|
| irrigated trees |
have two times higher needle-level daily net assimilation rate than control trees in mornings of |
June and August |
|
| drought |
can increase |
Tcrit by up to 2°C |
Pinus sylvestris |
| photosynthetic organisms on land |
emit |
molecular oxygen (O2) |
|
| Fucoxanthin (Fuco) |
is dominant in |
Phaeocystis globosa |
Phaeocystis globosa |
| light-absorbing pigment molecules |
participate in |
photosynthesis |
|
| downregulation of the (RBCL, ATCG00490) gene in red light |
evidenced |
inhibition of carbon fixation |
Phaeocystis globosa |
| seagrasses |
require |
relatively high in-water surface irradiances ranging from 10–37% relative to 0.1–1% for most other marine macrophytes |
Posidonia australis; Halophila uninervis |
| ferredoxin |
was measured in |
oscillating light of various frequencies |
Arabidopsis thaliana |
| frequency responses of apparent relative PC oxidation |
depend strongly on |
oscillation periods |
Arabidopsis thaliana |
| bundle-sheath (BS) cells of other C4 subtypes |
showed mixed decay of |
photosystem I (PSI) and photosystem II (PSII) |
|
| phosphorylation |
occurs in |
17 of 22 PSI–LHCI subunits |
Chlorella ohadii |
| plastids |
provide |
photosynthesis |
|
| Brassica rapa |
exhibits |
high photosynthesis rates |
Brassica rapa |
| net photosynthesis |
correlated positively and significantly with |
mesophyll conductance estimated from C-isotope discrimination |
Arabidopsis thaliana; Brassica nigra; Brassica rapa; Hirschfeldia incana |
| limitation by total diffusional conductance |
was not dominant in |
low-light-grown Hirschfeldia incana |
Hirschfeldia incana |
| thickness of cell wall and stroma |
correlated weakly with |
mesophyll conductance from combined gas exchange and chlorophyll fluorescence |
Arabidopsis thaliana; Brassica nigra; Brassica rapa; Hirschfeldia incana |
| more negative e* (e* = delta Ca-GE – delta Ca-growth) |
would result in |
higher apparent photosynthetic discrimination |
|
| green light excitation of Lhcp |
induced |
phosphorylation |
Ostreococcus tauri |
| FAsTeR method |
produces estimates of |
maximum assimilation rate (Amax) |
|
| BS chloroplasts in C2 species |
have relative number |
more than twice that in sunflower, S. flaveriae, and F. cronquistii |
Flaveria angustifolia; Flaveria sonorensis |
| enlarged bundle sheath (BS) cells of Solanum flaveriae and Flaveria cronquistii |
have |
increased their photosynthetic engagement |
Solanum flaveriae; Flaveria cronquistii |
| patterns of light fluctuations in terms of frequency, duration, and intensity |
determine |
ribulose 1,5-bisphosphate regeneration |
|
| intercellular CO2 concentration (Ci) |
is determined by |
mesophyll photosynthesis |
|
| Padina pavonica |
has |
Sc/o value among highest for Ochrophyta |
Padina pavonica |
| response to elevated CO2 |
requires quantitative process understanding on |
nonvascular photoautotrophs (NVP) under climate change |
|
| mesophyll conductance (gm) estimation |
assumes that |
resistance and gradient in the airspace are negligible |
|
| assimilation rate (A) in Helianthus annuus |
increased with |
ca as the latter varied from 50 to 500 μmol mol−1 |
Helianthus annuus |
| chloroplast-encoded photosynthesis genes (including the PSI and PSII core, ATP synthase) |
tend to be upregulated in response to |
all the nutrient-starvation, ROS, and low-temperature (at 72 h) treatments |
Thalassiosira pseudonana |
| chloroplast-encoded photosynthesis genes (including the PSI and PSII core, ATP synthase) |
are not differentially regulated in response to |
high-temperature |
Thalassiosira pseudonana |
| auxin |
may also regulate |
chloroplast function |
|
| species with C4 pathway |
may present photosynthetic advantages under |
P addition |
|
| light acclimation |
has role in shaping |
high light-induced chloroplast Ca2+ transients |
Chlamydomonas reinhardtii |
| photosynthetically active radiation |
is assumed to be absorbed at |
90% |
|
| flux density of photosynthetically active photon interception |
is assumed as |
90% for all photosynthetic types |
|
| simplified equations that dynamically partition sunlit and shaded leaf area |
have proven very effective for |
C4 crops |
|
| green light |
reduces photosynthesis (YII) to |
44.2% of absorbed light energy in Phaeocystis globosa during exponential growth |
Phaeocystis globosa |
| light regime |
varied significantly with |
photosynthetic activity of P. globosa |
Phaeocystis globosa |
| variation in light wavelength |
may adjust |
energy distribution |
|
| pgrl1ab mutation |
may impair |
linear electron transport |
Arabidopsis thaliana |
| frequency responses of apparent relative oxidation/reduction of P700 |
reveal |
diverging dynamics of components operating close to PSI |
Arabidopsis thaliana |
| quantum yield (Φ2) within NADP-ME subtype |
varied appreciably among |
species |
|
| percentage of bundle-sheath (BS) cell wall interfaced with mesophyll (M) cell (M/BS) |
correlated with |
bundle-sheath conductance (gbs) |
|
| PSI |
is far less sensitive to |
photodamage when compared to PSII |
Chlorella ohadii |
| dtn1-2 mutant |
shows significantly increased |
CO2 concentration (Ci) between cells |
Oryza sativa |
| MOC2 |
is |
photosynthesis-involved gene |
|
| interspecific variations in the specificity factor of Rubisco (SC/O) |
have been recognized across |
C3 plants |
|
| stomatal conductance to H2O under atmospheric conditions (gs400) |
is positively correlated with |
total leaf conductance to CO2 under atmospheric conditions (gtot400) |
|
| increase in Rubisco CO2/O2 specificity (SC/O,opt) with decreasing total leaf conductance (gtot400) |
would be attributed to |
physiological mechanism described above |
|
| least-cost theory (LCT) |
can be used to study |
coordination between carbon fixation and plant water use |
|
| greater electron transport rate |
as observed in |
Hirschfeldia incana |
Hirschfeldia incana |
| delta TR (ΔTR) |
is coupled more loosely to |
leaf-level gas exchange or delta C13 of leaf sugars or photosynthates |
|
| acclimation of photosynthetic rates to temperature |
seems to vary widely by |
species and location |
|
| fucoxanthin |
is |
important photosynthetic pigment in marine diatoms |
|
| ptATS2b mutant |
shows no difference in |
photosynthetic capacity compared to WT |
Phaeodactylum tricornutum |
| Rd intercept shift in F. sonorensis and F. angustifolia |
is |
only by slight amount |
Flaveria sonorensis; Flaveria angustifolia |
| electron transport chain (ETC) |
includes |
ferredoxin/flavodoxin NADP reductase (FNR) |
|
| hysteresis in stomatal responsiveness with the demand for CO2 |
erodes |
assimilation and water use efficiency (WUE) |
|
| pH in carboxysome |
will most likely be the same as in |
stroma |
|