Functional diversity of carbon-gain, water-use, and leaf-allocation traits in trees of a threatened lowland dry forest in Hawaii

2007 ◽  
Vol 94 (9) ◽  
pp. 1459-1469 ◽  
Author(s):  
Darren R. Sandquist ◽  
Susan Cordell
2019 ◽  
Vol 70 (1) ◽  
pp. 781-808 ◽  
Author(s):  
Andrew D.B. Leakey ◽  
John N. Ferguson ◽  
Charles P. Pignon ◽  
Alex Wu ◽  
Zhenong Jin ◽  
...  

The ratio of plant carbon gain to water use, known as water use efficiency (WUE), has long been recognized as a key constraint on crop production and an important target for crop improvement. WUE is a physiologically and genetically complex trait that can be defined at a range of scales. Many component traits directly influence WUE, including photosynthesis, stomatal and mesophyll conductances, and canopy structure. Interactions of carbon and water relations with diverse aspects of the environment and crop development also modulate WUE. As a consequence, enhancing WUE by breeding or biotechnology has proven challenging but not impossible. This review aims to synthesize new knowledge of WUE arising from advances in phenotyping, modeling, physiology, genetics, and molecular biology in the context of classical theoretical principles. In addition, we discuss how rising atmospheric CO2concentration has created and will continue to create opportunities for enhancing WUE by modifying the trade-off between photosynthesis and transpiration.


2020 ◽  
Vol 173 ◽  
pp. 104024
Author(s):  
Isadora Correia ◽  
Erivelton Rosário do Nascimento ◽  
Sidney F. Gouveia

2006 ◽  
Vol 3 (4) ◽  
pp. 421-437 ◽  
Author(s):  
A. Arneth ◽  
E. M. Veenendaal ◽  
C. Best ◽  
W. Timmermans ◽  
O. Kolle ◽  
...  

Abstract. We compare assimilation and respiration rates, and water use strategies in four divergent ecosystems located in cold-continental central Siberia and in semi-arid southern Africa. These seemingly unrelated systems have in common a harsh and highly seasonal environment with a very sharp transition between the dormant and the active season, with vegetation facing dry air and soil conditions for at least part of the year. Moreover, the northern high latitudes and the semi-arid tropics will likely experience changes in key environmental parameters (e.g., air temperature and precipitation) in the future; indeed, in some regions marked climate trends have already been observed over the last decade or so. The magnitude of instantaneous or daily assimilation and respiration rates, derived from one to two years of eddy covariance measurements in each of the four ecosystems, was not related to the growth environment. For instance, respiration rates were clearly highest in the two deciduous systems included in the analysis (a Mopane woodland in northern Botswana and a Downy birch forest in Siberia; >300 mmol m−2 d−1), while assimilation rates in the Mopane woodland were relatively similar to a Siberian Scots pine canopy for a large part of the active season (ca. 420 mmol m−2 d−1). Acknowledging the limited number of ecosystems compared here, these data nevertheless demonstrate that factors like vegetation type, canopy phenology or ecosystem age can override larger-scale climate differences in terms of their effects on carbon assimilation and respiration rates. By far the highest rates of assimilation were observed in Downy birch, an early successional species. These were achieved at a rather conservative water use, as indicated by relatively low levels of λ, the marginal water cost of plant carbon gain. Surprisingly, the Mopane woodland growing in the semi-arid environment had significantly higher values of λ. However, its water use strategy included a very plastic response to intermittently dry periods, and values of λ were much more conservative overall during a rainy season with low precipitation and high air saturation deficits. Our comparison demonstrates that forest ecosystems can respond very dynamically in terms of water use strategy, both on interannual and much shorter time scales. But it remains to be evaluated whether and in which ecosystems this plasticity is mainly due to a short-term stomatal response, or alternatively goes hand in hand with changes in canopy photosynthetic capacity.


1995 ◽  
Vol 22 (3) ◽  
pp. 461 ◽  
Author(s):  
J Vadell ◽  
C Cabot ◽  
H Medrano

The effects of drought acclimation on the diurnal time courses of photosynthesis and related characters were studied in Trifolium subterraneum L. leaves during two consecutive late spring days. Leaf CO2 assimilation rate and transpiration rate followed irradiance variations in irrigated plants. Under drought, a bimodal pattern of leaf CO2 assimilation rate developed although stomatal conductance remained uniform and low. Instantaneous water-use efficiency was much higher in droughted plants during the early morning and late evening, while during the middle of the day it was close to the value of irrigated plants. Net carbon gain in plants under drought reached 40% of the carbon gain in irrigated plants with a significant saving of water (80%). Average data derived from midday values of leaf CO2 assimilation rates and instantaneous water-use efficiency did not provide good estimates of the daily carbon gain and water-use efficiency for droughted leaves. Coupled with the morphological changes as a result of acclimation to progressive drought, modifications of diurnal patterns of leaf gas exchange rates effectively contribute to a sustained carbon gain during drought. These modifications significantly improve water-use efficiency, mainly by enabling the plant to take advantage of morning and evening hours with high air humidity.


Author(s):  
Kayla D. Stan ◽  
Arturo Sanchez-Azofeifa ◽  
Sandra M. Duran ◽  
Jose Antonio Guzmán Quesada ◽  
Michael Hesketh ◽  
...  

2014 ◽  
Vol 7 (5) ◽  
pp. 2193-2222 ◽  
Author(s):  
G. B. Bonan ◽  
M. Williams ◽  
R. A. Fisher ◽  
K. W. Oleson

Abstract. The Ball–Berry stomatal conductance model is commonly used in earth system models to simulate biotic regulation of evapotranspiration. However, the dependence of stomatal conductance (gs) on vapor pressure deficit (Ds) and soil moisture must be empirically parameterized. We evaluated the Ball–Berry model used in the Community Land Model version 4.5 (CLM4.5) and an alternative stomatal conductance model that links leaf gas exchange, plant hydraulic constraints, and the soil–plant–atmosphere continuum (SPA). The SPA model simulates stomatal conductance numerically by (1) optimizing photosynthetic carbon gain per unit water loss while (2) constraining stomatal opening to prevent leaf water potential from dropping below a critical minimum. We evaluated two optimization algorithms: intrinsic water-use efficiency (ΔAn /Δgs, the marginal carbon gain of stomatal opening) and water-use efficiency (ΔAn /ΔEl, the marginal carbon gain of transpiration water loss). We implemented the stomatal models in a multi-layer plant canopy model to resolve profiles of gas exchange, leaf water potential, and plant hydraulics within the canopy, and evaluated the simulations using leaf analyses, eddy covariance fluxes at six forest sites, and parameter sensitivity analyses. The primary differences among stomatal models relate to soil moisture stress and vapor pressure deficit responses. Without soil moisture stress, the performance of the SPA stomatal model was comparable to or slightly better than the CLM Ball–Berry model in flux tower simulations, but was significantly better than the CLM Ball–Berry model when there was soil moisture stress. Functional dependence of gs on soil moisture emerged from water flow along the soil-to-leaf pathway rather than being imposed a priori, as in the CLM Ball–Berry model. Similar functional dependence of gs on Ds emerged from the ΔAn/ΔEl optimization, but not the ΔAn /gs optimization. Two parameters (stomatal efficiency and root hydraulic conductivity) minimized errors with the SPA stomatal model. The critical stomatal efficiency for optimization (ι) gave results consistent with relationships between maximum An and gs seen in leaf trait data sets and is related to the slope (g1) of the Ball–Berry model. Root hydraulic conductivity (Rr*) was consistent with estimates from literature surveys. The two central concepts embodied in the SPA stomatal model, that plants account for both water-use efficiency and for hydraulic safety in regulating stomatal conductance, imply a notion of optimal plant strategies and provide testable model hypotheses, rather than empirical descriptions of plant behavior.


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