High concentrations of dissolved inorganic carbon in stems of herbaceous and woody C3plants exit leaves in the dark. In the light, C3species use a small portion of xylem‐transported CO2for leaf photosynthesis. However, it is not known if xylem‐transported CO2will exit leaves in the dark or be used for photosynthesis in the light in Kranz‐type C4plants. Cut leaves of In the dark, the efflux of xylem‐transported CO2increased with increasing rates of transpiration and [13CO2*]; however, rates of13Ceffluxin Kranz anatomy and biochemistry likely influence the efflux of xylem‐transported CO2out of cut leaves of
Traditionally, leaves were thought to be supplied with Cut leaves of The rates of assimilation and efflux of xylem‐transported The majority of xylem‐transported
- Award ID(s):
- 1301346
- NSF-PAR ID:
- 10443337
- Publisher / Repository:
- Wiley-Blackwell
- Date Published:
- Journal Name:
- New Phytologist
- Volume:
- 223
- Issue:
- 3
- ISSN:
- 0028-646X
- Page Range / eLocation ID:
- p. 1230-1240
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
Summary Amaranthus hypochondriacus were placed in one of three solutions of [NaH13CO3] dissolved in KCl water to measure the efflux of xylem‐transported CO2exiting the leaf in the dark or rates of assimilation of xylem‐transported CO2* in the light, in real‐time, using a tunable diode laser absorption spectroscope.A. hypochondriacus were lower compared to C3species. In the light,A. hypochondriacus fixed nearly 75% of the xylem‐transported CO2supplied to the leaf.A. hypochondriacus in the dark, as well as the use of xylem‐transported CO2* for photosynthesis in the light. Thus increasing the carbon use efficiency of Kranz‐type C4species over C3species. -
Summary Autotrophic respiration is a major driver of the global C cycle and may contribute a positive climate warming feedback through increased atmospheric concentrations of
CO 2. The extent of this feedback depends on plants' ability to acclimate respiration to maintain a constant carbon use efficiency (CUE ).We quantified respiratory partitioning of gross primary production (GPP) and
CUE of field‐grown trees in a long‐term warming experiment (+3°C). We delivered a13C–CO 2pulse to whole tree crowns and chased that pulse in the respiration of leaves, whole crowns, roots, and soil. We also measured the isotopic composition of soil microbial biomass and the respiration rates of leaves and whole crowns.We documented homeostatic respiratory acclimation of foliar and whole‐crown respiration rates; the trees adjusted to experimental warming such that leaf‐level respiration rates were not increased. Experimental warming had no detectable impact on respiratory partitioning or mean residence times. Of the13C label acquired by the trees, aboveground respiration consumed 10%, belowground respiration consumed 40%, and the remaining 50% was retained.
Experimental warming of +3°C did not alter respiratory partitioning at the scale of entire trees, suggesting that complete acclimation of respiration to warming is likely to dampen a positive climate warming feedback.
-
Summary Steady‐state photosynthetic
CO 2responses (A /C icurves) are used to assess environmental responses of photosynthetic traits and to predict future vegetative carbon uptake through modeling. The recent development of rapidA /C icurves (RAC iRs) permits faster assessment of these traits by continuously changing [CO 2] around the leaf, and may reveal additional photosynthetic properties beyond what is practical or possible with steady‐state methods.Gas exchange necessarily incorporates photosynthesis and (photo)respiration. Each process was expected to respond on different timescales due to differences in metabolite compartmentation, biochemistry and diffusive pathways. We hypothesized that metabolic lags in photorespiration relative to photosynthesis/respiration and
CO 2diffusional limitations can be detected by varying the rate of change in [CO 2] duringRAC iR assays. We tested these hypotheses through modeling and experiments at ambient and 2% oxygen.Our data show that photorespiratory delays cause offsets in predicted
CO 2compensation points that are dependent on the rate of change in [CO 2]. Diffusional limitations may reduce the rate of change in chloroplastic [CO 2], causing a reduction in apparentRAC iR slopes under highCO 2ramp rates.Multirate
RAC iRs may prove useful in assessing diffusional limitations to gas exchange and photorespiratory rates. -
Abstract The springtime transition to regional‐scale onset of photosynthesis and net ecosystem carbon uptake in boreal and tundra ecosystems are linked to the soil freeze–thaw state. We present evidence from diagnostic and inversion models constrained by satellite fluorescence and airborne
CO 2from 2012 to 2014 indicating the timing and magnitude of spring carbon uptake in Alaska correlates with landscape thaw and ecoregion. Landscape thaw in boreal forests typically occurs in late April (DOY 111 ± 7) with a 29 ± 6 day lag until photosynthetic onset. North Slope tundra thaws 3 weeks later (DOY 133 ± 5) but experiences only a 20 ± 5 day lag until photosynthetic onset. These time lag differences reflect efficient cold season adaptation in tundra shrub and the longer dehardening period for boreal evergreens. Despite the short transition from thaw to photosynthetic onset in tundra, synchrony of tundra respiration with snow melt and landscape thaw delays the transition from net carbon loss (at photosynthetic onset) to net uptake by 13 ± 7 days, thus reducing the tundra net carbon uptake period. Two globalCO 2inversions using aCASA ‐GFED model prior estimate earlier northern high latitude net carbon uptake compared to our regional inversion, which we attribute to (i) early photosynthetic‐onset model prior bias, (ii) inverse method (scaling factor + optimization window), and (iii) sparsity of available AlaskanCO 2observations. Another global inversion with zero prior estimates the same timing for net carbon uptake as the regional model but smaller seasonal amplitude. The analysis of Alaskan eddy covariance observations confirms regional scale findings for tundra, but indicates that photosynthesis and net carbon uptake occur up to 1 month earlier in evergreens than captured by models orCO 2inversions, with better correlation to above‐freezing air temperature than date of primary thaw. Further collection and analysis of boreal evergreen species over multiple years and at additional subarctic flux towers are critically needed. -
Summary Respiration in leaves and the continued elevation in the atmospheric
CO 2concentration causeCO 2‐mediated reduction in stomatal pore apertures. Several mutants have been isolated for which stomatal responses to both abscisic acid (ABA ) andCO 2are simultaneously defective. However, there are only few mutations that impair the stomatal response to elevatedCO 2, but not toABA . Such mutants are invaluable in unraveling the molecular mechanisms of earlyCO 2signal transduction in guard cells. Recently, mutations in the mitogen‐activated protein (MAP ) kinase, , have been shown to partially impairMPK 12CO 2‐induced stomatal closure. Here, we show thatmpk12 plants, in which is stably silenced specifically in guard cells (MPK 4mpk12 mpk4 homozygous double‐mutants), completely lackGC CO 2‐induced stomatal responses and have impaired activation of guard cell S‐type anion channels in response to elevatedCO 2/bicarbonate. However,ABA ‐induced stomatal closure, S‐type anion channel activation andABA ‐induced marker gene expression remain intact in thempk12 mpk4 double‐mutants. These findings suggest thatGC MPK 12 andMPK 4 act very early inCO 2signaling, upstream of, or parallel to the convergence ofCO 2andABA signal transduction. The activities ofMPK 4 andMPK 12 protein kinases were not directly modulated byCO 2/bicarbonatein vitro , suggesting that they are not directCO 2/bicarbonate sensors. Further data indicate thatMPK 4 andMPK 12 have distinguishable roles in Arabidopsis and that the previously suggested role ofRHC 1 in stomatalCO 2signaling is minor, whereasMPK 4 andMPK 12 act as key components of early stomatalCO 2signal transduction.