Free Standard AU & NZ Shipping For All Book Orders Over $80!
Register      Login
Functional Plant Biology Functional Plant Biology Society
Plant function and evolutionary biology
RESEARCH ARTICLE

Modelling seasonal and diurnal dynamics of stomatal conductance of plants in a semiarid environment

Qiong Gao A C , Mei Yu B , Xinshi Zhang A B , Hongmei Xu A and Yongmei Huang A
+ Author Affiliations
- Author Affiliations

A MOE Key Laboratory of Environmental Change and Natural Disasters, College of Resources Science and Technology, Beijing Normal University, Beijing 100875, People’s Republic of China.

B Institute of Botany, Chinese Academy of Sciences, Beijing 100093, People’s Republic of China.

C Corresponding author. Email: gaoq@bnu.edu.cn

Functional Plant Biology 32(7) 583-598 https://doi.org/10.1071/FP04092
Submitted: 25 May 2004  Accepted: 19 April 2005   Published: 7 July 2005

Abstract

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 surface. The model can be easily adapted to ecosystem simulation because of its mathematical simplicity. Guard-cell osmotic pressure at zero light intensity, apparent elastic modulus of guard cells per leaf area, half-saturation light intensity, maximum light-inducible osmotic pressure, soil-to-leaf resistance at zero plant water potential, sensitivity of soil-to-leaf resistance to xylem water potential, and plant body water capacitance, are independent parameters of the model. The model was fitted to the field data of the five species with a non-linear least-square algorithm to obtain the parameters. The result indicates that the model explained, on average, 88% of seasonal and diurnal variation of stomatal conductance for the five species, in comparison with 67% of variation explained by an early model without plant body water capacitance. Comparisons of the physiological parameters among the species show that the woody species exhibited more tolerance for water stresses than the forb because of their higher dark osmotic pressure, greater capability of seasonal and diurnal osmotic regulation, and stiffer guard cell structure (or smaller stomatal density or both). A decreasing trend of soil-to-leaf resistance from the trees to the shrubs to the forb was found in this study. Midday depression of transpiration and stomatal conductance may or may not occur, depending on the magnitude of body water capacitance.

Key words: drought tolerance and resistance, gas exchange, guard cell function, leaf transpiration, Loess Plateau, northern China, plant water capacitance, stomata opening.


Acknowledgments

This research was jointly supported by the Chinese Ministry of Science and Technology grant #G2000018605, and the National Science Foundation of China grants #90202008 and #90211002, and BNU Innovation Team Funds for Synthetic Landscape Dynamics.


References


Aphalo PJ, Jarvis PG (1991) Do stomata respond to relative humidity. Plant, Cell & Environment 14, 127–132. open url image1

Ball, JT , Woodrow, IE ,  and  Berry, JA (1987). A model predicting stomatal conductance and its contribution to the control of photosynthesis under different environmental conditions. In ‘Progress in photosynthesis research’. pp. 221–224. (Martinus Nijhoff Publishers: Dordrecht)

Buckley TN, Mott KA, Farquhar GD (2003) A hydromechanical and biochemical model of stomatal conductance. Plant, Cell & Environment 26, 1767–1785.
Crossref | GoogleScholarGoogle Scholar | open url image1

Campbell GS, Jungbauer JD, Shiozawa S, Hungerford RD (1993) A one-parameter equation for water sorption isotherms of soils. Soil Science 156, 302–305. open url image1

Campbell, GS ,  and  Norman, JM (1998). ‘An introduction to environmental biophysics.’ 2nd edn. edn . (Springer-Verlag: New York)

Cheung YNS, Tyree MT, Dainty J (1975) Water relations parameters on single leaves obtained in a pressure bomb and some ecological interpretations. Canadian Journal of Botany 53, 1342–1346. open url image1

Collatz GJ, Ball JT, Grivet C, Berry JA (1991) Physiological and environmental regulation of stomatal conductance photosynthesis and transpiration, a model that includes a laminar boundary layer. Agricultural and Forest Meteorology 54, 107–136.
Crossref | GoogleScholarGoogle Scholar | open url image1

Cooke JR, DeBaerdemaeker JG, Rand RH, Mang HA (1976) A finite element shell analysis of guard cell deformations. Transactions of the American Society of Agricultural Engineers 19, 1107–1121. open url image1

Dewar RC (1995) Interpretation of an empirical model for stomatal conductance in terms of guard cell function. Plant, Cell & Environment 18, 365–372. open url image1

Dewar RC (2002) The Ball–Berry–Leuning and Tardieu–Davies stomatal models: synthesis and extension within a spatially aggregated picture of guard cell function. Plant, Cell & Environment 25, 1383–1398.
Crossref | GoogleScholarGoogle Scholar | open url image1

Dong X, Zhang X (2001) Some observations of the adaptations of sandy shrubs to the arid environment in the Mu Us Sandland: leaf water relations and anatomic features. Journal of Arid Environments 48, 41–48.
Crossref | GoogleScholarGoogle Scholar | open url image1

Farquhar GB, Wong SC (1984) An empirical model of stomatal conductance. Australian Journal of Plant Physiology 11, 191–210. open url image1

Forseth IN, Wait DA, Casper BB (2001) Shading by shrubs in a desert system reduces the physiological and demographic performance of an associated herbaceous perennial. Journal of Ecology 89, 670–680.
Crossref | GoogleScholarGoogle Scholar | open url image1

Franks PJ, Cowan IR, Farquhar GD (1997) The apparent feedforward response of stomata to air vapour pressure deficit: information revealed by different experimental procedures with two rainforest trees. Plant, Cell & Environment 20, 142–145.
Crossref | GoogleScholarGoogle Scholar | open url image1

Franks PJ, Cowan IR, Farquhar GD (1998) A study of stomatal mechanics using the cell pressure probe. Plant, Cell & Environment 21, 94–100.
Crossref | GoogleScholarGoogle Scholar | open url image1

Gao Q, Zhao P, Zeng X, Cai X, Shen W (2002) A model of stomata conductance to quantify the relationship between plant transpiration and microclimate and soil water stress. Plant, Cell & Environment 25, 1373–1381.
Crossref | GoogleScholarGoogle Scholar | open url image1

Gao Q (1996) Dynamic modeling of ecosystem with spatial heterogeneity, a structured approach implemented in Windows environment. Ecological Modelling 85, 241–252.
Crossref | GoogleScholarGoogle Scholar | open url image1

Gao Q, Xu LD, Liang N (2001) Dynamic modelling with an integrated ecological knowledge-based system. Knowledge-Based Systems 14, 281–287.
Crossref | GoogleScholarGoogle Scholar | open url image1

Gao Q, Reynolds JF (2003) Historical shrub-grass transition in the northern Chihuahuan Desert: modeling the effects of shifting rainfall seasonality and event size over a landscape gradient. Global Change Biology 9, 1475–1493.
Crossref | GoogleScholarGoogle Scholar | open url image1

Guo W (2004) ‘Effects of water stress on eco-physiological characteristics of two major afforestation shrubs.’ PhD Thesis (Shandong University: China)

Jacobs CMJ, Vandenhurk BJJM, Debruin HAR (1996) Stomatal behaviour and photosynthetic rate of unstressed grapevines in semi-arid conditions. Agricultural and Forest Meteorology 80, 111–134.
Crossref | GoogleScholarGoogle Scholar | open url image1

Kalapos T, Vandenboogaard R, Lambers H (1996) Effect of soil drying on growth, biomass allocation and leaf gas exchange of two annual grass species. Plant and Soil 185, 137–149. open url image1

Kemp PR, Reynolds JF, Pachepsky Y, Chen J-L (1997) A comparative modelling study of soil water dynamics in a desert ecosystem. Water Resources Research 33, 73–90.
Crossref | GoogleScholarGoogle Scholar | open url image1

Knapp AK, Cocke M, Hamerlynck EP, Owensby CE (1994a) Effect of elevated CO2 on stomatal density and distribution in a C-4 grass and a C-3 forb under field conditions. Annals of Botany 74, 595–599.
Crossref | GoogleScholarGoogle Scholar | open url image1

Knapp AK, Fahnestock JT, Owensby CE (1994b) Elevated atmospheric CO2 alters stomatal responses to variable sunlight in a C-4 grass. Plant, Cell & Environment 17, 189–195. open url image1

Knapp AK, Hamerlynck EP, Ham JM, Owensby CE (1996) Responses in stomatal conductance to elevated CO2 in 12 grassland species that differ in growth form. Vegetatio 125, 31–41.
Crossref | GoogleScholarGoogle Scholar | open url image1

Leuning R (1995) A critical appraisal of a combined stomatal-photosynthesis model for C3 plants. Plant, Cell & Environment 18, 339–355. open url image1

Li, S , Fang, T ,  and  Yoshikawa, K (1992). A study on the PV curves of several trees in the Maowusu Sands. In ‘Collected papers of the Maowusu Sands Exploitation and Control Research Center’. pp. 160–164. (Publisher of Inner Mongolia University: Huhehot, China)

Liu MZ, Jiang GM, Li YG, Niu SL (2003) Leaf osmotic potentials of 104 plant species in relation to habitats and plant functional types in Hunshandak sandland, Inner Mongolia, China. Trees 17, 554–560.
Crossref | GoogleScholarGoogle Scholar | open url image1

Lu P, Yunusa IA, Walker RR, Muller WJ (2003) Regulation of canopy conductance and transpiration and their modelling in irrigated grapevines Functional Plant Biology 30, 689–698.
Crossref | GoogleScholarGoogle Scholar | open url image1

Monson RK, Smith SD (1982) Seasonal water potential components of Sonoran Desert (Arizona, USA) plants. Ecology 63, 113–123. open url image1

Mooney HA, Field C, Vazquez-Yanes C, Chu C (1983) Environmental controls on stomatal conductance in a shrub of the humid tropics. Proceedings of the National Academy of Sciences USA 80, 1295–1297. open url image1

Mott KA, Parkhurst DF (1991) Stomatal response to humidity in air and helox. Plant, Cell & Environment 14, 509–515. open url image1

Muchow RC (1985) Stomatal behavior in grain legumes grown under different soil water regimes in a semi-arid tropical environment. Field Crops Research 11, 291–307.
Crossref | GoogleScholarGoogle Scholar | open url image1

Nijs I, Ferris R, Blum H, Hendrey G, Impens I (1997) Stomatal regulation in a changing climate: a field study using free air temperature increase (FATI) and free air CO2 enrichment (FACE). Plant, Cell & Environment 20, 1041–1050. open url image1

Nilsen ET, Sharifi MR, Rundel PW, Jarrell WM, Virginia RA (1983) Diurnal and seasonal water relations of the desert phreatophyte Prosopis glandulosa (honey mesquite) in the Sonoran Desert of California (USA). Ecology 64, 1381–1393. open url image1

Nobel, PS (1983). ‘Biophysical plant physiology and ecology.’ (W. H. Freeman and Company: New York)

Noe SM, Giersch C (2004) A simple dynamic model of photosynthesis in oak leaves: coupling leaf conductance and photosynthetic carbon fixation by a variable intracellular CO2 pool. Functional Plant Biology 31, 1195–1204.
Crossref | GoogleScholarGoogle Scholar | open url image1

Odening WR, Strain BR, Oechel WC (1974) The effect of decreasing water potential on net CO2 exchange of intact desert shrubs. Ecology 55, 1086–1095. open url image1

Peek MS, Alexander ERCD, Forseth IN (2002) Physiological response curve analysis using nonlinear mixed models. Oecologia 132, 175–180.
Crossref | GoogleScholarGoogle Scholar | open url image1

Reynolds, JF , Kemp, PR , Acock, B , Chen, J-L ,  and  Moorhead, DL (1996). Progress, limitations, and challenge in modeling the effects of elevated CO2 on plant and ecosystems. In ‘Carbon dioxide and terrestrial ecosystems’. pp. 374–380. (Academic Press: San Diego , CA)

Reynolds JF, Virginia RA, Kemp PR, Soyza AGD, Tremel DC (1999) Impact of drought on desert shrubs: effects of seasonality and degree of resource island development. Ecological Monographs 69, 69–106. open url image1

Ritchie GA, Hinckley TM (1975) The pressure chamber as an instrument for ecological research. Advances in Ecological Research 9, 165–254. open url image1

Ryel RJ, Caldwell MM, Yoder CK, Or D, Leffler AJ (2002) Hydraulic redistribution in a stand of Artemisia tridentata: evaluation of benefits to transpiration assessed with a simulation model. Oecologia 130, 173–184. open url image1

Schultz HR (2003) 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, 673–687.
Crossref | GoogleScholarGoogle Scholar | open url image1

Sellin A (1996) Base water potential of Picea abies as a characteristic of the soil water status. Plant and Soil 184, 273–280. open url image1

Sellin A (1999) Does pre-dawn water potential reflect conditions of equilibrium in plant and soil water status? Acta Oecologia 20, 51–59.
Crossref | GoogleScholarGoogle Scholar | open url image1

Snyder KA, Richards JH, Donovan LA (2003) Night-time conductance in C3 and C4 species: do plants lose water at night? Journal of Experimental Botany 54, 861–865..
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Thornley, JM ,  and  Johnston, IR (1990). ‘Plant and crop modelling.’ (Clarendon Press: Oxford)

Xu H, Gao Q, Huang Y, Jia H (2004) Photosynthetic characteristics of 6 plant species in the steppe-forest regions in the Loess Plateau. Acta Phytoecologica Sinica 28, 157–163. open url image1