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1

Leuning, R. "Modelling Stomatal Behaviour and and Photosynthesis of Eucalyptus grandis." Functional Plant Biology 17, no. 2 (1990): 159. http://dx.doi.org/10.1071/pp9900159.

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Stomatal conductances, CO2 assimilation, transpiration and intercellular CO2 mol fractions of Eucalyptus grandis leaves were measured in the field using a portable, controlled environment cuvette. Test leaves were subjected to a range of temperatures, humidities, photon irradiances and external CO2 mol fractions. An empiral function, gsw = g0 + g1 Ahs/(cs-I'), was able to account for steady- state stomatal conductances g*sw, over a wide range of environmental conditions and leaf photosynthetic capacities. In this equation, termed the stomatal constraint function, A is CO2 assimilation rate, hs
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2

Anderegg, William R. L. "Quantifying seasonal and diurnal variation of stomatal behavior in a hydraulic-based stomatal optimization model." Journal of Plant Hydraulics 5 (December 22, 2018): e001. http://dx.doi.org/10.20870/jph.2018.e001.

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Plant responses to drought occur across many time-scales, with stomatal closure typically considered to be a critical short-term response. Recent theories of optimal stomatal conductance linked to plant hydraulic transport have shown promise, but it is not known if stomata update their hydraulic “shadow price” of water use (marginal increase in carbon cost with a marginal drop in water potential) over days, seasons, or in response to recent drought. Here, I estimate the hydraulic shadow price in five species – two semi-arid gymnosperms, one temperate and two tropical angiosperms – at daily tim
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3

Buchholcerová, Anna, Peter Fleischer, Dušan Štefánik, Svetlana Bičárová, and Veronika Lukasová. "Specification of Modified Jarvis Model Parameterization for Pinus cembra." Atmosphere 12, no. 11 (2021): 1388. http://dx.doi.org/10.3390/atmos12111388.

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The high ambient ozone concentrations cause impairing effects on vegetation leading to plant injuries. The potential ozone uptake to vegetation through open stomata can be quantified using stomatal conductance measurements under the local environmental conditions. This study compares the ozone stomatal conductance to vegetation obtained with a modified Jarvis formula adopted from the Vegetation Manual of United Nations Economic Commission for Europe, and experimental field measurements’ data. The stomatal conductance was measured by a portable photosynthesis and gas exchange analyzer system Li
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4

Sun, Ruifeng, Juanjuan Ma, Xihuan Sun, Shijian Bai, Lijian Zheng, and Jiachang Guo. "Study on a Stomatal Conductance Model of Grape Leaves in Extremely Arid Areas." Sustainability 15, no. 10 (2023): 8342. http://dx.doi.org/10.3390/su15108342.

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Stomata are essential for regulating the exchange of water and energy between plants and the atmosphere. In the context of climate warming, especially in extremely arid regions, the knowledge of stomatal conductance variation patterns is fundamental to the study of crop evapotranspiration, productivity and drought resistance characteristics. The accurate simulation of stomatal conductance in this region is an important prerequisite for the optimal regulation of the crop growth environment. In this study, a two-year field experiment was carried out in vineyards in an extremely arid region. The
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5

Yun, Kyungdahm, Dennis Timlin, and Soo-Hyung Kim. "Coupled Gas-Exchange Model for C4 Leaves Comparing Stomatal Conductance Models." Plants 9, no. 10 (2020): 1358. http://dx.doi.org/10.3390/plants9101358.

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Plant simulation models are abstractions of plant physiological processes that are useful for investigating the responses of plants to changes in the environment. Because photosynthesis and transpiration are fundamental processes that drive plant growth and water relations, a leaf gas-exchange model that couples their interdependent relationship through stomatal control is a prerequisite for explanatory plant simulation models. Here, we present a coupled gas-exchange model for C4 leaves incorporating two widely used stomatal conductance submodels: Ball–Berry and Medlyn models. The output varia
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6

Li, Qianyu, Shawn P. Serbin, Julien Lamour, Kenneth J. Davidson, Kim S. Ely, and Alistair Rogers. "Implementation and evaluation of the unified stomatal optimization approach in the Functionally Assembled Terrestrial Ecosystem Simulator (FATES)." Geoscientific Model Development 15, no. 11 (2022): 4313–29. http://dx.doi.org/10.5194/gmd-15-4313-2022.

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Abstract. Stomata play a central role in regulating the exchange of carbon dioxide and water vapor between ecosystems and the atmosphere. Their function is represented in land surface models (LSMs) by conductance models. The Functionally Assembled Terrestrial Ecosystem Simulator (FATES) is a dynamic vegetation demography model that can simulate both detailed plant demographic and physiological dynamics. To evaluate the effect of stomatal conductance model formulation on forest water and carbon fluxes in FATES, we implemented an optimality-based stomatal conductance model – the Medlyn (MED) mod
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7

Han, Tuo, Qi Feng, Tengfei Yu, Xiaomei Yang, Xiaofang Zhang, and Kuan Li. "Characteristic of Stomatal Conductance and Optimal Stomatal Behaviour in an Arid Oasis of Northwestern China." Sustainability 14, no. 2 (2022): 968. http://dx.doi.org/10.3390/su14020968.

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Stomatal conductance (gs), the process that governs plant carbon uptake and water loss, is fundamental to most Land Surface Models (LSMs). With global change accelerating, more attention should be paid to investigating stomatal behavior, especially in extremely arid areas. In this study, gas exchange measurements and environmental/biological variables observations during growing seasons in 2016 and 2017 were combined to investigate diurnal and seasonal characteristics of gs and the applicability of the optimal stomatal conductance model in a desert oasis vineyard. The results showed that the r
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8

Bauerle*, William L., and Joe E. Toler. "Stomatal Control by Both Abscisic Acid in the Bulk Leaf Tissue and Leaf Environment: A Test of a Model of Stomatal Conductance to Leaf Environment Coupled with an Abscisic Acid-based Model." HortScience 39, no. 4 (2004): 855B—855. http://dx.doi.org/10.21273/hortsci.39.4.855b.

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A multiplicative model of stomatal conductance was developed and tested in two functionally distinct ecotypes of Acer rubrum L. (red maple). The model overcomes the main limitation of the commonly used Ball-Berry model by accounting for stomatal behavior under soil drying conditions. It combined the Ball-Berry model with an integrated expression of abscisic acid-based control mechanisms (gfac). The factor gfac = exp(-β[ABA]L) incorporated the stomatal response to abscisic acid (ABA) concentration in the bulk leaf tissue [ABA]L into the Ball-Berry model by down-regulating the slope and coupled
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9

McCaughey, J. Harry, and Antonio Iacobelli. "Modelling stomatal conductance in a northern deciduous forest, Chalk River, Ontario." Canadian Journal of Forest Research 24, no. 5 (1994): 904–10. http://dx.doi.org/10.1139/x94-119.

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Modelling results of stomatal conductance of trembling aspen (Populustremuloides Michx.) and white birch (Betulapapyrifera Marsh.) are reported. Stomatal conductance for the two species was related to global solar radiation, vapour pressure deficit, and air temperature using both linear and nonlinear least squares approaches. Both approaches provided an equally poor fit when relating the large scatter of stomatal conductance data to each of the environmental variables separately. However, an additive, multiple linear regression model and a multiplicative, nonlinear least squares model were abl
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10

Lombardozzi, D., S. Levis, G. Bonan, and J. P. Sparks. "Predicting photosynthesis and transpiration responses to ozone: decoupling modeled photosynthesis and stomatal conductance." Biogeosciences Discussions 9, no. 4 (2012): 4245–83. http://dx.doi.org/10.5194/bgd-9-4245-2012.

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Abstract. Plants exchange carbon dioxide and water, two key greenhouse gases, with the atmosphere through the processes of photosynthesis and transpiration, making them essential in climate regulation. Carbon dioxide and water exchange are typically coupled through the control of stomatal conductance, and the parameterization in many models often predict conductance based on photosynthesis values. Some environmental conditions, like exposure to high ozone (O3) concentrations, alter photosynthesis independent of stomatal conductance, so models cannot accurately predict both. The goals of this s
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11

Lombardozzi, D., S. Levis, G. Bonan, and J. P. Sparks. "Predicting photosynthesis and transpiration responses to ozone: decoupling modeled photosynthesis and stomatal conductance." Biogeosciences 9, no. 8 (2012): 3113–30. http://dx.doi.org/10.5194/bg-9-3113-2012.

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Abstract. Plants exchange greenhouse gases carbon dioxide and water with the atmosphere through the processes of photosynthesis and transpiration, making them essential in climate regulation. Carbon dioxide and water exchange are typically coupled through the control of stomatal conductance, and the parameterization in many models often predict conductance based on photosynthesis values. Some environmental conditions, like exposure to high ozone (O3) concentrations, alter photosynthesis independent of stomatal conductance, so models that couple these processes cannot accurately predict both. T
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12

Bonan, G. B., M. Williams, R. A. Fisher, and K. W. Oleson. "Modeling stomatal conductance in the earth system: linking leaf water-use efficiency and water transport along the soil–plant–atmosphere continuum." Geoscientific Model Development 7, no. 5 (2014): 2193–222. http://dx.doi.org/10.5194/gmd-7-2193-2014.

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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 pho
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13

Bonan, G. B., M. Williams, R. A. Fisher, and K. W. Oleson. "Modeling stomatal conductance in the Earth system: linking leaf water-use efficiency and water transport along the soil-plant-atmosphere continuum." Geoscientific Model Development Discussions 7, no. 3 (2014): 3085–159. http://dx.doi.org/10.5194/gmdd-7-3085-2014.

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Abstract. The empirical 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 both 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) to numerically optimize photosynthetic carbon gain per unit wate
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14

De Kauwe, M. G., J. Kala, Y. S. Lin, et al. "A test of an optimal stomatal conductance scheme within the CABLE Land Surface Model." Geoscientific Model Development Discussions 7, no. 5 (2014): 6845–91. http://dx.doi.org/10.5194/gmdd-7-6845-2014.

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Abstract. Stomatal conductance (gs) affects the fluxes of carbon, energy and water between the vegetated land surface and the atmosphere. We test an implementation of an optimal stomatal conductance model within the Community Atmosphere Biosphere Land Exchange (CABLE) land surface model (LSM). In common with many LSMs, CABLE does not differentiate between gs model parameters in relation to plant functional type (PFT), but instead only in relation to photosynthetic pathway. We therefore constrained the key model parameter "g1" which represents a plants water use strategy by PFT based on a globa
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15

Grossnickle, Steven C., and John H. Russell. "Gas exchange processes of yellow-cedar (Chamaecyparis nootkatensis) in response to environmental variables." Canadian Journal of Botany 69, no. 12 (1991): 2684–91. http://dx.doi.org/10.1139/b91-337.

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Yellow-cedar (Chamaecyparis nootkatensis (D. Don) Spach) gas exchange processes were measured in response to the following primary environmental variables: photosynthetically active radiation, vapour pressure deficit, root temperature, and soil moisture. Under nonlimiting edaphic conditions, maximum stomatal conductance and maximum CO2 assimilation increased rapidly as photosynthetically active radiation increased from 0 to 200 μmol∙m−2∙s−1 and from 0 to 500 μmol∙m−2∙s−1, respectively. Thereafter, greater photosynthetically active radiation levels only resulted in minor increases in stomatal c
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16

Nguyen, Thuy Huu, Matthias Langensiepen, Jan Vanderborght, Hubert Hüging, Cho Miltin Mboh, and Frank Ewert. "Comparison of root water uptake models in simulating CO<sub>2</sub> and H<sub>2</sub>O fluxes and growth of wheat." Hydrology and Earth System Sciences 24, no. 10 (2020): 4943–69. http://dx.doi.org/10.5194/hess-24-4943-2020.

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Abstract. Stomatal regulation and whole plant hydraulic signaling affect water fluxes and stress in plants. Land surface models and crop models use a coupled photosynthesis–stomatal conductance modeling approach. Those models estimate the effect of soil water stress on stomatal conductance directly from soil water content or soil hydraulic potential without explicit representation of hydraulic signals between the soil and stomata. In order to explicitly represent stomatal regulation by soil water status as a function of the hydraulic signal and its relation to the whole plant hydraulic conduct
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17

De Kauwe, M. G., J. Kala, Y. S. Lin, et al. "A test of an optimal stomatal conductance scheme within the CABLE land surface model." Geoscientific Model Development 8, no. 2 (2015): 431–52. http://dx.doi.org/10.5194/gmd-8-431-2015.

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Abstract. Stomatal conductance (gs) affects the fluxes of carbon, energy and water between the vegetated land surface and the atmosphere. We test an implementation of an optimal stomatal conductance model within the Community Atmosphere Biosphere Land Exchange (CABLE) land surface model (LSM). In common with many LSMs, CABLE does not differentiate between gs model parameters in relation to plant functional type (PFT), but instead only in relation to photosynthetic pathway. We constrained the key model parameter "g1", which represents plant water use strategy, by PFT, based on a global synthesi
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18

Xue, Runjia, Wenjun Zuo, Zhaowen Zheng, et al. "Interpreting Controls of Stomatal Conductance across Different Vegetation Types via Machine Learning." Water 16, no. 16 (2024): 2251. http://dx.doi.org/10.3390/w16162251.

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Plant stomata regulate transpiration (T) and CO2 assimilation, essential for the water–carbon cycle. Quantifying how environmental factors influence stomatal conductance will provide a scientific basis for understanding the vegetation–atmosphere water–carbon exchange process and water use strategies. Based on eddy covariance and hydro-metrological observations from FLUXNET sites with four plant functional types and using three widely applied methods to estimate ecosystem T from eddy covariance data, namely uWUE, Perez-Priego, and TEA, we quantified the regulation effect of environmental factor
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19

McMurtrie, Ross E., Richard J. Norby, Belinda E. Medlyn, et al. "Why is plant-growth response to elevated CO2 amplified when water is limiting, but reduced when nitrogen is limiting? A growth-optimisation hypothesis." Functional Plant Biology 35, no. 6 (2008): 521. http://dx.doi.org/10.1071/fp08128.

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Experimental evidence indicates that the stomatal conductance and nitrogen concentration ([N]) of foliage decline under CO2 enrichment, and that the percentage growth response to elevated CO2 is amplified under water limitation, but reduced under nitrogen limitation. We advance simple explanations for these responses based on an optimisation hypothesis applied to a simple model of the annual carbon–nitrogen–water economy of trees growing at a CO2-enrichment experiment at Oak Ridge, Tennessee, USA. The model is shown to have an optimum for leaf [N], stomatal conductance and leaf area index (LAI
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20

Lloyd, J., T. Trochoulias, and R. Ensbey. "Stomatal Responses and Whole-Tree Hydraulic Conductivity of Orchard Macadamia integrifolia Under Irrigated and Non-Irrigated Conditions." Functional Plant Biology 18, no. 6 (1991): 661. http://dx.doi.org/10.1071/pp9910661.

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Diurnal patterns of stomatal conductance (gs) and leaf water potential (Ψ1) were determined for leaves on irrigated and non-irrigated 5-year-old Macadamia integrifolia trees over a 4-month period from September to December 1989. An empirical model for stomatal conductance was developed for irrigated trees using relationships to photon irradiance (I), leaf temperature (T1) and vapour mole fraction difference (D). This model accounted for 69% of the variance in gs, and was not improved by the inclusion of Ψ1 as an independent variable. Fitted parameters led to the effective prediction of gs for
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21

Liao, Qi, Risheng Ding, Taisheng Du, Shaozhong Kang, Ling Tong, and Shuai Li. "Salinity-specific stomatal conductance model parameters are reduced by stomatal saturation conductance and area via leaf nitrogen." Science of The Total Environment 876 (June 2023): 162584. http://dx.doi.org/10.1016/j.scitotenv.2023.162584.

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22

Wehr, Richard, Róisín Commane, J. William Munger, et al. "Dynamics of canopy stomatal conductance, transpiration, and evaporation in a temperate deciduous forest, validated by carbonyl sulfide uptake." Biogeosciences 14, no. 2 (2017): 389–401. http://dx.doi.org/10.5194/bg-14-389-2017.

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Abstract. Stomatal conductance influences both photosynthesis and transpiration, thereby coupling the carbon and water cycles and affecting surface–atmosphere energy exchange. The environmental response of stomatal conductance has been measured mainly on the leaf scale, and theoretical canopy models are relied on to upscale stomatal conductance for application in terrestrial ecosystem models and climate prediction. Here we estimate stomatal conductance and associated transpiration in a temperate deciduous forest directly on the canopy scale via two independent approaches: (i) from heat and wat
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23

BUCKLEY, T. N., K. A. MOTT, and G. D. FARQUHAR. "A hydromechanical and biochemical model of stomatal conductance." Plant, Cell & Environment 26, no. 10 (2003): 1767–85. http://dx.doi.org/10.1046/j.1365-3040.2003.01094.x.

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24

Qu, Mingnan, Saber Hamdani, Wenzhen Li, et al. "Rapid stomatal response to fluctuating light: an under-explored mechanism to improve drought tolerance in rice." Functional Plant Biology 43, no. 8 (2016): 727. http://dx.doi.org/10.1071/fp15348.

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Light inside a canopy constantly fluctuates. Under fluctuating light (FL) conditions, stomatal conductance and photosynthetic rate constantly change. In this study, we explored whether this dynamics of stomata movements upon FL influenced the water use efficiency of rice in the field. We used a USDA-curated rice mini-core diversity panel consisting of 204 worldwide distributed accessions. A priori model on dynamic stomatal response to FL was utilised to identify kinetic parameters describing the stomatal delays during the closing (τcl) and the opening (τop) phase. Result showed that τcl had a
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25

Liu, Ke, Yujie Wang, Troy S. Magney, and Christian Frankenberg. "Non-steady-state stomatal conductance modeling and its implications: from leaf to ecosystem." Biogeosciences 21, no. 6 (2024): 1501–16. http://dx.doi.org/10.5194/bg-21-1501-2024.

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Abstract. Accurate and efficient modeling of stomatal conductance (gs) has been a key challenge in vegetation models across scales. Current practice of most land surface models (LSMs) assumes steady-state gs and predicts stomatal responses to environmental cues as immediate jumps between stationary regimes. However, the response of stomata can be orders of magnitude slower than that of photosynthesis and often cannot reach a steady state before the next model time step, even on half-hourly timescales. Here, we implemented a simple dynamic gs model in the vegetation module of an LSM developed w
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26

Gowdy, Mark, Bruno Suter, Philippe Pieri, et al. "Variety-specific response of bulk stomatal conductance of grapevine canopies to changes in net radiation, atmospheric demand, and drought stress." OENO One 56, no. 2 (2022): 205–22. http://dx.doi.org/10.20870/oeno-one.2022.56.2.5435.

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In wine growing regions around the world, climate change has the potential to affect vine transpiration and overall vineyard water use due to related changes in daily atmospheric conditions and soil water deficits. Grapevines control their transpiration in response to such changes by regulating conductance of water through the soil-plant-atmosphere continuum. The response of bulk stomatal conductance, the vine canopy equivalent of stomatal conductance, to such changes were studied on Cabernet-Sauvignon, Merlot, Tempranillo, Ugni blanc, and Semillon vines in a non-irrigated vineyard in Bordeaux
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27

Lombardozzi, Danica L., Melanie J. B. Zeppel, Rosie A. Fisher, and Ahmed Tawfik. "Representing nighttime and minimum conductance in CLM4.5: global hydrology and carbon sensitivity analysis using observational constraints." Geoscientific Model Development 10, no. 1 (2017): 321–31. http://dx.doi.org/10.5194/gmd-10-321-2017.

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Abstract. The terrestrial biosphere regulates climate through carbon, water, and energy exchanges with the atmosphere. Land-surface models estimate plant transpiration, which is actively regulated by stomatal pores, and provide projections essential for understanding Earth's carbon and water resources. Empirical evidence from 204 species suggests that significant amounts of water are lost through leaves at night, though land-surface models typically reduce stomatal conductance to nearly zero at night. Here, we test the sensitivity of carbon and water budgets in a global land-surface model, the
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28

Martin, Marion J., Peter K. Farage, Steve W. Humphries, and Steve P. Long. "Can the stomatal changes caused by acute ozone exposure be predicted by changes occurring in the mesophyll? A simplification for models of vegetation response to the global increase in tropospheric elevated ozone episodes." Functional Plant Biology 27, no. 3 (2000): 211. http://dx.doi.org/10.1071/pp99132.

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The prediction of complex interactive effects of rising concentrations of ozone and CO2on vegetation will require robust models based on mechanistic understanding of how these two gases affect photosynthesis. This paper describes the development of a model of acute ozone exposure effects on wheat leaf photosynthesis, based on the mechanism of reactive oxygen scavenging processes. Based on experimental data, the dose of ozone to the leaf above a threshold flux, here termed the effective ozone dose, was found to be linearly related to the decline in the in vivo maximum rate of carboxylation. The
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29

Mäkelä, Jarmo, Jürgen Knauer, Mika Aurela, et al. "Parameter calibration and stomatal conductance formulation comparison for boreal forests with adaptive population importance sampler in the land surface model JSBACH." Geoscientific Model Development 12, no. 9 (2019): 4075–98. http://dx.doi.org/10.5194/gmd-12-4075-2019.

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Abstract. We calibrated the JSBACH model with six different stomatal conductance formulations using measurements from 10 FLUXNET coniferous evergreen sites in the boreal zone. The parameter posterior distributions were generated by the adaptive population importance sampler (APIS); then the optimal values were estimated by a simple stochastic optimisation algorithm. The model was constrained with in situ observations of evapotranspiration (ET) and gross primary production (GPP). We identified the key parameters in the calibration process. These parameters control the soil moisture stress funct
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Gao, Qiong, Mei Yu, Xinshi Zhang, Hongmei Xu, and Yongmei Huang. "Modelling seasonal and diurnal dynamics of stomatal conductance of plants in a semiarid environment." Functional Plant Biology 32, no. 7 (2005): 583. http://dx.doi.org/10.1071/fp04092.

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Seasonal and diurnal stomatal conductance, leaf transpiration, and soil water contents of two shrubs of Hippophae rhamnoides L. subsp. Sinensis Rousi and Caragana korshinskii Kom., two trees of Malus pomila Mill. and Robinia pseudoacacia L., and a forb, Artemisia gmelinii, were measured in field of the semiarid Loess Plateau, north China, during the growing season of 2002. We developed a dynamic, nonlinear semi-mechanistic model to relate stomatal conductance of these plants to soil water potential, incident photon flux density, vapour pressure deficit, and partial CO2 pressure, on leaf surfac
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31

TUZET, A., A. PERRIER, and R. LEUNING. "A coupled model of stomatal conductance, photosynthesis and transpiration." Plant, Cell & Environment 26, no. 7 (2003): 1097–116. http://dx.doi.org/10.1046/j.1365-3040.2003.01035.x.

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32

Aphalo, P. "An Analysis of Ball's Empirical Model of Stomatal Conductance." Annals of Botany 72, no. 4 (1993): 321–27. http://dx.doi.org/10.1006/anbo.1993.1114.

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33

Schultz, Hans R. "Extension of a Farquhar model for limitations of leaf photosynthesis induced by light environment, phenology and leaf age in grapevines (Vitis vinifera L. cvv. White Riesling and Zinfandel)." Functional Plant Biology 30, no. 6 (2003): 673. http://dx.doi.org/10.1071/fp02146.

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Measurements of gas exchange and stomatal conductance were made on potted and field-grown grapevines (Vitis vinifera L.) on leaves from different light environments (sun and shade) at different phenological stages during the season to parameterise the Farquhar model. The model parameters for Rubisco activity (Vcmax), maximum electron transport rate (Jmax), and triose-phosphate utilisation (TPU) were estimated on the basis of a large data set (n = 105) of CO2 assimilation (A) versus internal CO2 pressure (Ci) curves. Leaf age was described with the leaf plastochron index (LPI). Stomatal couplin
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34

K.Kalaichelvi. "Physiological Efficiency of Weeds in Rice Fallow Fields." International Journal of Plant & Soil Science 36, no. 5 (2024): 323–28. http://dx.doi.org/10.9734/ijpss/2024/v36i54530.

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Photosynthetic rate, Transpiration rate and Stomatal Conductance is measured in different weeds during July’2020 in rice fallows using IRGA- Photosynthesis system model Lci- T. We have chosen all the weeds at flowering to maturity phase and observed the data. Among the weeds analysed Parthenium hysterophorus has recorded very high Photosynthetic rate (µ molm-2 Sec-1)and there was difference with stage also, Flowering stage (165.28) has recorded a higher photosynthetic rate followed by vegetative (123.2) and maturity phase (118.72) and found that transpiration rate also followed the same trend.
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35

Green, S. R., T. M. Mills, and B. E. Clothier. "Seasonal Water Use of a Kiwifruit Vine: Measurements and a Model." HortScience 32, no. 3 (1997): 446G—447. http://dx.doi.org/10.21273/hortsci.32.3.446g.

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We recorded canopy development and stomatal function of a kiwifruit vine for the purpose of calculating the seasonal water use by the crop. Canopy development was described using an empirical “S-shaped” curve fitted to weekly measurements of the vine's leaf area. Stomatal conductance was described using a semi-empirical model based on the incident radiation, and the ambient vapor pressure deficit of the air. These two descriptors, leaf area and stomatal conductance, were combined with meteorological data to calculate vine transpiration via the Penman–Monteith model. Transpiration rates calcula
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36

Lombardozzi, D. L., M. J. B. Zeppel, R. A. Fisher, and A. Tawfik. "Observed nighttime conductance alters modeled global hydrology and carbon budgets." Geoscientific Model Development Discussions 8, no. 12 (2015): 10339–63. http://dx.doi.org/10.5194/gmdd-8-10339-2015.

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Abstract. The terrestrial biosphere regulates climate through carbon, water, and energy exchanges with the atmosphere. Land surface models estimate plant transpiration, which is actively regulated by stomatal pores, and provide projections essential for understanding Earth's carbon and water resources. Empirical evidence from 204 species suggests that significant amounts of water are lost through leaves at night, though land surface models typically reduce stomatal conductance to nearly zero at night. Here, we apply observed nighttime stomatal conductance values to a global land surface model,
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Ranawana, S. R. W. M. C. J. K., K. H. M. Siddique, J. A. Palta, K. Stefanova, and H. Bramley. "Stomata coordinate with plant hydraulics to regulate transpiration response to vapour pressure deficit in wheat." Functional Plant Biology 48, no. 9 (2021): 839. http://dx.doi.org/10.1071/fp20392.

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Genotypic variation in transpiration (Tr) response to vapour pressure deficit (VPD) has been studied in many crop species. There is debate over whether shoots or roots drive these responses. We investigated how stomata coordinate with plant hydraulics to mediate Tr response to VPD and influence leaf water status in wheat (Triticum aestivum L.). We measured Tr and stomatal conductance (gs) responses to VPD in well-watered, water-stressed and de-rooted shoots of eight wheat genotypes. Tr response to VPD was related to stomatal sensitivity to VPD and proportional to gs at low VPD, except in the w
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Hoshika, Yasutomo, Elena Paoletti, and Kenji Omasa. "Parameterization of Zelkova serrata stomatal conductance model to estimate stomatal ozone uptake in Japan." Atmospheric Environment 55 (August 2012): 271–78. http://dx.doi.org/10.1016/j.atmosenv.2012.02.083.

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Wang, Shusen. "Evaluation of Water Stress Impact on the Parameter Values in Stomatal Conductance Models Using Tower Flux Measurement of a Boreal Aspen Forest." Journal of Hydrometeorology 13, no. 1 (2012): 239–54. http://dx.doi.org/10.1175/jhm-d-11-043.1.

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Abstract The impact of water stress on plant stomatal conductance (g) has been widely studied but with little consensus as to the processes governing its responses. The photosynthesis-driven stomatal conductance models usually employ constant model parameters and attribute the decrease of g from water stress to the reduction of leaf photosynthesis. This has been challenged by studies showing that the model parameter values decrease when the plant is under water stress. In this study, the impact of plant water stress on the parameter values in stomatal conductance models is evaluated using the
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Piayda, A., M. Dubbert, C. Rebmann, et al. "Drought impact on carbon and water cycling in a Mediterranean <i>Quercus suber</i> L. woodland during the extreme drought event in 2012." Biogeosciences 11, no. 24 (2014): 7159–78. http://dx.doi.org/10.5194/bg-11-7159-2014.

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Abstract. Savannah-type ecosystems account for 26–30% of global gross primary productivity GPP, with water being one of the major driving factors. In Europe, savannah-type woodlands cover an area of about 1.5 million ha. Here, the recent past has shown a significant decrease in precipitation P in winter and spring as well as a decrease in total annual precipitation. Strong effects on local water balance and carbon sink strength have thus been reported due to changes in precipitation regime. The objective of this study is to quantify the impact of the extreme drought event in 2012 on the water
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Piayda, A., M. Dubbert, C. Rebmann, et al. "Drought impact on carbon and water cycling in a Mediterranean <i>Quercus suber</i> L. woodland during the extreme drought event in 2012." Biogeosciences Discussions 11, no. 7 (2014): 10365–417. http://dx.doi.org/10.5194/bgd-11-10365-2014.

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Abstract. Savannah-type ecosystems account for 26–30% of global gross primary productivity GPP with water being one of the major driving factors. In Europe, savannah-type woodlands cover an area of about 1.5 million ha. Here, the recent past has shown a significant decrease of precipitation P in winter and spring as well as decrease of total annual precipitation. Strong effects on local water balance and carbon sink strength have thus been reported due to changes in precipitation regime. The objective of this study is to quantify the impact of the extreme drought event in 2012 on the water bal
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Allen, Leon H., Mary P. Brakke, and James W. Jones. "SIMULATION OF TRANSPIRATION OF CITRUS GOVERNED BY LEAF CONDUCTANCE." HortScience 27, no. 6 (1992): 609d—609. http://dx.doi.org/10.21273/hortsci.27.6.609d.

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A water flow model was developed which uses irradiance, leaf-to-air vapor concentration difference, and soil water potential to establish stomatal conductance. Water flow to the roots was computed using a linear approximation of radial flow through the soil toward the axis of the roots across concentric shells. Root length density and soil rooting volume within four separate layers or compartments were included in the model. The simulation was executed in small time step iterations. A small increment of transpiration was translated to a water content deficit at the root and then sequentially t
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Hu, Meng, Shao Zhong Kang, Tai Sheng Du, and Ling Tong. "Another View of Gas Exchange Model: Reflection of Leaf Surface Air to Stomatal Conductance." Advanced Materials Research 113-116 (June 2010): 14–17. http://dx.doi.org/10.4028/www.scientific.net/amr.113-116.14.

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A reflection function was established, based on leaf gas exchange process and tested with experimental data of eight kinds of plants, i.e. tomato, muskmelon, capsicum, maize, grape, onion, Haloxylon Ammodendron Bunge and Caragana Karshiskii Kom, with multifarious biological characteristic, water and growing status. The function indicated that the leaf stomatal conductance could be linearly reflected by the ratio of humidity and CO2 concentration at leaf surface, and the behaviour of its slope could be recognized as an indicator of leaf gas exchange efficiency, which had a negative relationship
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Kala, J., M. G. De Kauwe, A. J. Pitman, et al. "Implementation of an optimal stomatal conductance model in the Australian Community Climate Earth Systems Simulator (ACCESS1.3b)." Geoscientific Model Development Discussions 8, no. 7 (2015): 5235–64. http://dx.doi.org/10.5194/gmdd-8-5235-2015.

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Abstract. We implement a new stomatal conductance model, based on the optimality approach, within the Community Atmosphere Biosphere Land Exchange (CABLE) land surface model. Coupled land-atmosphere simulations are then performed using CABLE within the Australian Community Climate and Earth Systems Simulator (ACCESS) with prescribed sea surface temperatures. As in most land surface models, the default stomatal conductance scheme only accounts for differences in model parameters in relation to the photosynthetic pathway, but not in relation to plant functional types. The new scheme allows model
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Gong, Cheng, Yadong Lei, Yimian Ma, Xu Yue, and Hong Liao. "Ozone–vegetation feedback through dry deposition and isoprene emissions in a global chemistry–carbon–climate model." Atmospheric Chemistry and Physics 20, no. 6 (2020): 3841–57. http://dx.doi.org/10.5194/acp-20-3841-2020.

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Abstract. Ozone–vegetation feedback is essential to tropospheric ozone (O3) concentrations. The O3 stomatal uptake damages leaf photosynthesis and stomatal conductance and, in turn, influences O3 dry deposition. Further, O3 directly influences isoprene emissions, an important precursor of O3. The effects of O3 on vegetation further alter local meteorological fields and indirectly influence O3 concentrations. In this study, we apply a fully coupled chemistry–carbon–climate global model (ModelE2-YIBs) to evaluate changes in O3 concentrations caused by O3–vegetation interactions. Different parame
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Ewers, B. E., R. Oren, K. H. Johnsen, and J. J. Landsberg. "Estimating maximum mean canopy stomatal conductance for use in models." Canadian Journal of Forest Research 31, no. 2 (2001): 198–207. http://dx.doi.org/10.1139/x00-159.

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Fertilized (F) and irrigated and fertilized (IF) stands of Pinus taeda L. produced twice the leaf area index of irrigated (I) and control (C) stands. Based on sap flux-scaled mean stomatal conductance (GS), we found that stomatal conductance in F was half that in other treatments. During the growing season, GS was related to vapor pressure deficit (D) and soil moisture. During the cooler season, soil moisture was high and light accompanied D in controlling GS. Under all conditions and treatments, the rate of decrease in GS with D was proportional to GS at low D (= 1 kPa). We evaluated whether
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Barbour, Margaret M., Lucas A. Cernusak, David Whitehead та ін. "Nocturnal stomatal conductance and implications for modelling δ18O of leaf-respired CO2 in temperate tree species". Functional Plant Biology 32, № 12 (2005): 1107. http://dx.doi.org/10.1071/fp05118.

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Variation in the oxygen isotope composition of within-canopy CO2 has potential to allow partitioning of the ecosystem respiratory flux into above- and below-ground components. Recent theoretical work has highlighted the sensitivity of the oxygen isotope composition of leaf-respired CO2 (δRl) to nocturnal stomatal conductance. When the one-way flux model was tested on Ricinus communis L. large enrichments in δRl were observed. However, most species for which the isotope flux partitioning technique has been or would be applied (i.e. temperate tree species) are much more conservative users of wat
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de la Torre Llorente, Daniel. "Comparison of Several Models for Calculating Ozone Stomatal Fluxes on a Mediterranean Wheat Cultivar (Triticum durumDesf. cv. Camacho)." Scientific World JOURNAL 7 (2007): 1634–48. http://dx.doi.org/10.1100/tsw.2007.243.

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Ozone stomatal fluxes were modeled for a 3-year period following different approaches for a commercial variety of durum wheat (Triticum durumDesf. cv. Camacho) at the phenological stage of anthesis. All models performed in the same range, although not all of them afforded equally significant results. Nevertheless, all of them suggest that stomatal conductance would account for the main percentage of ozone deposition fluxes. A new modeling approach was tested, based on a 3-D architectural model of the wheat canopy, and fairly accurate results were obtained. Plant species-specific measurements,
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Anav, Alessandro, Chiara Proietti, Laurent Menut, Stefano Carnicelli, Alessandra De Marco, and Elena Paoletti. "Sensitivity of stomatal conductance to soil moisture: implications for tropospheric ozone." Atmospheric Chemistry and Physics 18, no. 8 (2018): 5747–63. http://dx.doi.org/10.5194/acp-18-5747-2018.

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Abstract. Soil moisture and water stress play a pivotal role in regulating stomatal behaviour of plants; however, in the last decade, the role of water availability has often been neglected in atmospheric chemistry modelling studies as well as in integrated risk assessments, despite the fact that plants remove a large amount of atmospheric compounds from the lower troposphere through stomata. The main aim of this study is to evaluate, within the chemistry transport model CHIMERE, the effect of soil water limitation on stomatal conductance and assess the resulting changes in atmospheric chemist
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Gibert, Caroline, Michel Génard, Gilles Vercambre, and Françoise Lescourret. "Quantification and modelling of the stomatal, cuticular and crack components of peach fruit surface conductance." Functional Plant Biology 37, no. 3 (2010): 264. http://dx.doi.org/10.1071/fp09118.

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This study describes the components of fruit surface conductance. It aims to revise a modelling framework examining water loss across the fruit epidermis in relation to time and fruit growing conditions. For this purpose, cuticular crack surface area, healing artificial wounds in vivo, stomatal number and total fruit surface conductance were quantified during nectarine (Prunus persica L. nucipersica) fruit growth under contrasted irrigation regimes or thinning intensities. The contribution of stomatal component to total conductance decreased very early. A sub-model of the specific cuticular co
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