Apparent responses of stomata to transpiration and humidity in a hybrid poplar canopy

It has been proposed that the stomatal response to humidity relies on sensing of the transpiration rate itself rather than relative humidity or the saturation deficit per se. We used independent measurements of stomatal conductance (g_s), transpiration (E), and leaf-to-air vapour pressure difference (V) in a hybrid poplar canopy to evaluate relationships between g_s and E and between g_s and V. Relationships between E, V and total vapour phase conductance or crown conductance (g_c) were also assessed. Conductance measurements were made on exposed and partially shaded branches over a wide range of incident solar radiation. In exposed branches, g_s appeared to decline linearly with increasing E and increasing V at both high and low irradiance. However, in a partially shaded branch, a bimodal relationship between g_s and E was observed in which g_s continued to decrease after E had reached a maximum value and begun to decrease. The relationship between g_s and V for this branch was linear. Plots of g_c against E always yielded bimodal or somewhat variable relationships, whereas plots of g_c against V were invariably linear. It was not possible to derive a unique relationship between conductance and E or V because prevailing radiation partially determined the operating range for conductance. Normalization of data by radiation served to linearize responses observed within the same day or type of day, but even after normalization, data collected on partly cloudy days could not be used to predict stomatal behaviour on clear days and vice versa. An additional unidentified factor was thus also involved in determining operating ranges of conductance on days with different overall radiation regimes. We suggest that the simplest mechanism to account for the observed humidity responses is stomatal sensing of the epidermal or cuticular transpiration rate rather than the bulk leaf or stomatal transpiration rate.     

Environmental and physiological regulation of transpiration in tropical forest gap species: the influence of boundary layer and hydraulic properties

Environmental and physiological regulation of transpiration were examined in several gap-colonizing shrub and tree species during two consecutive dry seasons in a moist, lowland tropical forest on Barro Colorado Island, Panama. Whole plant transpiration, stomatal and total vapor phase (stomatal + boundary layer) conductance, plant water potential and environmental variables were measured concurrently. This allowed control of transpiration (E) to be partitioned quantitatively between stomatal (g _s) and boundary layer (g _b) conductance and permitted the impact of invividual environmental and physiological variables on stomatal behavior and E to be assessed. Wind speed in treefall gap sites was often below the 0.25 m s^–1 stalling speed of the anemometer used and was rarely above 0.5 m s^–1, resulting in uniformly low g _b (c. 200–300 mmol m^–2 s^–1) among all species studied regardless of leaf size. Stomatal conductance was typically equal to or somewhat greater than g _b. This strongly decoupled E from control by stomata, so that in Miconia argentea a 10% change in g _s when g _s was near its mean value was predicted to yield only a 2.5% change in E. Porometric estimates of E, obtained as the product of g _s and the leaf-bulk air vapor pressure difference (VPD) without taking g _b into account, were up to 300% higher than actual E determined from sap flow measurements. Porometry was thus inadequate as a means of assessing the physiological consequences of stomatal behavior in different gap colonizing species. Stomatal responses to humidity strongly limited the increase in E with increasing evaporative demand. Stomata of all species studied appeared to respond to increasing evaporative demand in the same manner when the leaf surface was selected as the reference point for determination of external vapor pressure and when simultaneous variation of light and leaf-air VPD was taken into account. This result suggests that contrasting stomatal responses to similar leaf-bulk air VPD may be governed as much by the external boundary layer as by intrinsic physiological differences among species. Both E and g _s initially increased sharply with increasing leaf area-specific total hydraulic conductance of the soil/root/leaf pathway (G _t), becoming asymptotic at higher values of G _t. For both E and g _s a unique relationship appeared to describe the response of all species to variations in G _t. The relatively weak correlation observed between g _s and midday leaf water potential suggested that stomatal adjustment to variations in water availability coordinated E with water transport efficiency rather than bulk leaf water status.     

Control of transpiration in an irrigated Eucalyptus globulus Labill. plantation

Stomatal conductance and transpiration were measured concurrently in an irrigated Eucalyptus globulus Labill. plantation. Canopy stomatal conductance, canopy boundary layer conductance and the dimensionless decoupling coefficient (Ω) were calculated (a) summing the conductance of three canopy layers (g_c) and (b) weighting the contribution of foliage according to the amount of radiation received (g_c′). Canopy transpiration was then calculated from g_c and g_c′ for Ω = 1 (E_eq), Ω = 0 (E_imp) and by weighting E_eq and E_imp using Ω (E_Ω). E_eq, E_imp and E_Ω were compared to transpiration estimated from measurements of heat pulse velocity. The mean value of Ω was 0·63. Transpiration calculated using g_c and assuming perfect coupling (12·5 ± 0·9 mmol m^?2 s^?1) significantly overestimated measured values (8·7 ± 0·8 mmol m^?2 s^?1). Good estimates of canopy transpiration were obtained either (a) calculating E_Ω separately for the individual canopy layers or (b) treating the canopy as a single layer and using g_c′ in a calculation of E_imp (Ω = 0). The latter approach only required measurement of stomatal conductance at a single canopy position but would be unsuitable for use in combined models of canopy transpiration and assimilation. It should however, be suitable for estimating transpiration in forests regardless of the degree of coupling.     

Regulation of transpiration in coffee hedgerows: covariation of environmental variables and apparent responses of stomata to wind and humidity

Stomatal regulation of transpiration was studied in hedgerow coffee (Coffea arabica L.) at different stages of canopy development encompassing a range of leaf area indices (L) from 0·7 to 6·7. Stomatal (g_s) and crown (g_c) conductance attained maximum values early during the day and then declined as both leaf-to-bulk air water vapour mole fraction difference (V_a) and photosynthetically active photon flux density (I) continued to increase. Covariation of environmental variables during the day, particularly V, I, and wind speed (u), obscured stomatal responses to individual variables. This also caused diurnal hysteresis in the relationship between g_c and individual variables. Normalization of g_s and g_c by I removed the hysteresis and revealed a strong stomatal response to humidity. At the crown scale, transpiration (E) increased linearly with net radiation (R_n) and seemed to increase with increasing wind speed. Increasing wind speed imposed higher leaf interior to leaf surface water vapour mole fraction differences (V_s) at given levels of V_a. However, strong relationships between declining g_c and E and increasing wind speed were obtained when g_c and E were normalized by I and R_n, respectively, without invoking additional potential interactions involving temperature or CO₂ concentration at the leaf surface. Apparent stomatal responses to wind were thus at least partially a reflection of the stomatal response to humidity.     

Late-stage canopy tree species with extremely low δ13C and high stomatal sensitivity to seasonal soil drought in the tropical rainforest of French Guiana

We assessed the daily time‐courses of CO₂ assimilation rate (A), leaf transpiration rate (E), stomatal conductance for water vapour (g_s), leaf water potential ( Ψ _w) and tree transpiration in a wet and a dry season for three late‐stage canopy rainforest tree species in French Guiana differing in leaf carbon isotope composition ( δ ¹³C). The lower sunlit leaf δ ¹³C values found in Virola surinamensis ( ? 29·9‰) and in Diplotropis purpurea ( ? 30·9‰), two light‐demanding species, as compared to Eperua falcata ( ? 28·6‰), a shade‐semi‐tolerant species, were clearly associated with higher maximum g_s values of sunlit leaves in the two former species. These two species were also characterized by a high sensitivity of g_s, sap flow density (Ju) and canopy conductance (g_c) to seasonal soil drought, allowing maintenance of high midday Ψ _w values in the dry season. The data for Diplotropis provided an original picture of increasing midday Ψ _w with increasing soil drought. In Virola, stomata were extremely sensitive to seasonal soil drought, leading to a dramatic decrease in leaf and tree transpiration in the dry season, whereas midday Ψ _w remained close to ? 0·3 MPa. The mechanisms underlying such an extremely high sensitivity of stomata to soil drought remain unknown. In Eperua, g_s of sunlit leaves was non‐responsive to seasonal drought, whereas Ju and g_c were lower in the dry season. This suggests a higher stomatal sensitivity to seasonal drought in shaded leaves than in sunlit ones in this species.     

Stomatal and environmental control of transpiration in a lowland tropical forest tree

Stomatal control of crown transpiration was studied in Anacardium excelsum, a large-leaved, emergent canopy species common in the moist forests of Central and northern South America. A construction crane equipped with a gondola was used to gain access to the uppermost level in the crown of a 35-m-tall individual. Stomatal conductance at the single leaf scale, and transpiration and total vapour phase conductance (stomatal and boundary layer) at the branch scale were measured simultaneously using the independent techniques of porometry and stem heat balance, respectively. This permitted the sensitivity of transpiration to a marginal change in stomatal conductance to be evaluated using a dimensionless coupling coefficient (1-ω) ranging from zero to 1, with 1 representing maximal stomatal control of transpiration. Average stomatal conductance varied from 0.09 mol m^?2 s^?1 during the dry season to 0.3 mol m^?2 s^?1 during the wet season. Since boundary layer conductance was relatively low (0.4 mol m^?2 s^?1), 1-ω ranged from 0.46 during the dry season to only 0.25 during the wet season. A pronounced stomatal response to humidity was observed, which strongly limited transpiration as evaporative demand increased. The stomatal response to humidity was apparent only when the leaf surface was used as the reference point for measurement of external vapour pressure. Average transpiration was predicted to be nearly the same during the dry and wet seasons despite a 1 kPa difference in the prevailing leaf-to-air vapour pressure difference. The patterns of stomatal behaviour and transpiration observed were consistent with recent proposals that stomatal responses to humidity are based on sensing the transpiration rate itself.     

The boundary layer and the apparent responses of stomatal conductance to wind speed and to the mole fractions of CO2 and water vapour in the air

The experiments and simulations reported in this paper show that, for stomata sensitive to both CO₂ and water vapour concentrations, responses of stomatal conductance (g^w_s) to boundary layer thickness have two components, one resulting from changes in intercellular CO₂ concentration (χ^c_i) and another from changes in leaf surface water vapour saturation deficit (D^w_s). The experiments and simulations also show that the boundary layer conductance (g^w_b) can significantly alter the apparent response of g^w_s to ambient air CO₂ mole fraction (χ^c_a) and water vapour mole fraction (χ^w_a). Because of the feedback loop involved the responses of g^w_s for χ^c_a and χ^w_a each include responses to both χ^c_i and D^w_s. The boundary layer alters the state of the variables sensed by the guard cells—i.e. χ^c_i and D^w_s—and so it is a source of feedback. Thus, when scaling up from responses of stomata to the response of g^w_s for a whole leaf, the effect of the boundary layer must be considered. The results indicate that, for given responses of g^w_s to χ^c_i and D^w_s, the apparent responses of g^w_s to D^w_a and χ^c_a depend on the size of the leaf and wind speed, showing that this effect of the boundary layer should be considered when comparing data measured under different conditions, or with different methods.     

Estimating transpiration from 6-year-old Eucalyptus grandis trees: development of a canopy conductance model and comparison with independent sap flux measurements

Daily patterns of stomatal conductance (g_s), xylem pressure potential (P) and canopy microclimatic variables were recorded on 11 sample days as part of a one-year study of the water use of Eucalyptus grandis Hill ex Maiden in the eastern Transvaal, South Africa. Measured g_s was found to be largely controlled by quantum flux density (Q) and ambient vapour pressure deficit (D). Canopy conductance (g_c) was determined for hourly intervals using g_s measurements and leaf areas in four different canopy levels. A simple model was constructed to allow the prediction of g_c and transpiration from Q, D and season of year. The model was used to estimate transpiration rates from 10 trees in a later study of similarly-aged E. grandis trees, in which sap flow in each tree was measured using the heat pulse velocity (HPV) technique. Five of the trees were monitored on a summer day and five on a winter day. Correspondence between HPV sap flow and modelled transpiration was good for the summertime comparisons, but measured winter-time sap flow rates were underestimated by the model, especially under conditions of high sap flow. The discrepancy is believed to result from having insufficient data from the conductance study to describe the response of g_s to relatively high D in winter. Marked variation in transpiration per unit leaf area indicates that a relatively large number of trees must be sampled for the HPV technique to be used to obtain a mean rate for an entire stand in winter.     

Stomatal behaviour in a beech canopy: an analysis of Bowen ratio measurements compared with porometer data

On the basis of measurements or stand transpiration and microclimate, the bulk stomatal or bulk leaf conductance (g_L) of a beech forest in northern Germany was calculated for periods in which leaves were fully expanded and the canopy was dry. This conductance depends strongly on light and humidity conditions above the forest. During periods with photosynthetic photon flux densities Q > 1200 μmol m^?2s^?1, g_L was reduced from 1500mmol m^?2s^?1 at a vapour pressure deficit D= 0.5kPa to 500 mmol m^?2s^?1 at D= 2kPa. Light saturation of g_L was not reached until Q= 1200 μmol m^?2s^?1 at low D, or until even higher Q at higher D. The dependence of g_L, on Q and D was described mathematically by a non-linear equation that requires two empirical parameters. Values for g_L as simulated by this equation provided a satisfactory agreement with independent porometer data collected on single leaves and scaled up to the canopy. A comparison of stomatal and aerodynamic conductances showed a strong coupling between the forest canopy and the atmosphere, indicating that transpiration of the beech forest is controlled mainly by the stomata.     

Influence of stomatal distribution on transpiration in low-wind environments

Abstract According to computer energy balance simulations of horizontal thin leaves, the quantitative effects of stomatal distribution patterns (top vs. bottom surfaces) on transpiration (E) were maximal for sunlit leaves with high stomatal conductances (g_s) and experiencing low windspeeds (free or mixed convection regimes). E of these leaves decreased at windspeeds > 50 cm s^?1, despite increases in the leaf-to-air vapour density deficit. At 50 cm s^?1 wind-speed, rapidly transpiring leaves had greater E when one-half of the stomata were on each leaf surface (amphistomaty; 10.16 mmol H₂O m^?2 s^?1) than when all stomata were on either the top (hyperstomaty; 9.34 mmol m^?2s^?1) or bottom (hypostomaty; 7.02 mmol m^?2s^?1) surface because water loss occurred in parallel from both surfaces. Hyperstomatous leaves had larger E than hypostomatous leaves because free convection was greater on the top than on the bottom surface. Transpiration of leaves with large g, was greatest at windspeeds near zero when ～60–75% of the stomata were on the top surface, while at high windspeeds E was greatest with, 50% of the stomata on top. For leaves with low g_s, stomatal distribution exerted little influence on simulated E values. Laboratory measurements of water loss from simulated hypo-, hyper-, and amphistomatous leaf models qualitatively supported these predictions.     

Influences of PAR, temperature and water vapor concentration on gas exchange by ferns

The effects of photosynthetically active radiation (PAR), leaf temperature and the leaf-to-air water vapor concentration drop on net CO₂ uptake and water vapor conductance were surveyed for 14 species of ferns. Most previous studies indicated that ferns have extremely low maximal rates of net CO₂ uptake, below 2 umol m^?2 s^?1, whereas the average maximal rate observed here at 25⁰ C was 7 umol m^?2 s^?1. Net CO₂ uptake reached 90% of saturation at an average PAR (400 to 700 nm) of only 240 umol m^?2 s^?1, consistent with the typically shaded habitats of most ferns. Maximal CO₂ uptake rates were positively correlated with the PAR for 90% saturation (r²=0.59), the chlorophyII per unit leaf area (r²=0.30), the water vapor conductance (r²=0.65), and the CO₂ residual conductance (r²=0.69). A higher water vapor conductance (gwv) was correlated with a greater fractional change in gwv as the leaf-to-air water vapor concentration drop (Δc_wv) was raised from 5to20 g m^?3 (r²=0.90). Specifically, for species with low g_wv of about I mm s^?1 the ratio of g_wv at Δc_wv= 5 g m^?3 to that at Δc_wv= 20 g m^?3 was near 1, but it was near 2 for species with g_wv of about 4 mm s^?1. Such a relationship, which can prevent excessive transpiration, has apparently not previously been pointed out in surveys of other plant groups.     

Regulation of water flux through trunks, branches, and leaves in trees of a lowland tropical forest

We studied regulation of whole-tree water use in individuals of five diverse canopy tree species growing in a Panamanian seasonal forest. A construction crane equipped with a gondola was used to access the upper crowns and points along the branches and trunks of the study trees for making concurrent measurements of sap flow at the whole-tree and branch levels, and vapor phase conductances and water status at the leaf level. These measurements were integrated to assess physiological regulation of water use from the whole-tree to the single-leaf scale. Whole-tree water use ranged from 379 kg day⁻¹ in a 35 m-tall Anacardium excelsum tree to 46 kg day⁻¹ in an 18 m-tall Cecropia longipes tree. The dependence of whole-tree and branch sap velocity and sap flow on sapwood area was essentially identical in the five trees studied. However, large differences in transpiration per unit leaf area (E) among individuals and among branches on the same individual were observed. These differences were substantially reduced when E was normalized by the corresponding branch leaf area:sapwood area ratio (LA/SA). Variation in stomatal conductance (g _s) and crown conductance (g _c), a total vapor phase conductance that includes stomatal and boundary layer components, was closely associated with variation in the leaf area-specific total hydraulic conductance of the soil/leaf pathway (G _t). Vapor phase conductance in all five trees responded similarly to variation in G _t. Large diurnal variations in G _t were associated with diurnal variation in exchange of water between the transpiration stream and internal stem storage compartments. Differences in stomatal regulation of transpiration on a leaf area basis appeared to be governed largely by tree size and hydraulic architectural features rather than physiological differences in the responsiveness of stomata. We suggest that reliance on measurements gathered at a single scale or inadequate range of scale may result in misleading conclusions concerning physiological differences in regulation of transpiration. Received: 1 October 1997 / Accepted: 6 March 1998     

Control of transpiration in three coffee cultivars: the role of hydraulic and crown architecture

Water use and hydraulic architecture were studied in the coffee (Coffea arabica) cultivars San Ramon, Yellow Caturra and Typica growing in the field under similar environmental conditions. The cultivars differed in growth habit, crown architecture, basal sapwood area and total leaf surface area. Transpiration per unit leaf area (E), stomatal conductance (g _s), crown conductance (g _c), total hydraulic conductance of the soil/leaf pathway (G _t) and the stomatal decoupling coefficient, omega (Ω) (Jarvis and McNaughton 1986) were assessed over a range of soil moisture and during partial defoliation treatments. The relationship between sap flow and sapwood area was linear and appeared to be similar for the three cultivars. Variation in g _c, E, and G _t of intact plants and leaf area-specific hydraulic conductivity (k _l) of excised lateral branches was negatively correlated with variation in the ratio of leaf area to sapwood area. Transpiration, g _c, and g _s were positively correlated with G _t. Transpiration and G _t varied with total leaf area and were greatest at intermediate values (10 m²) of leaf area. Omega was greatest in Yellow Caturra, the cultivar with the greatest leaf area and a dense crown, and was smallest in Typica, the cultivar with an open crown. Differences in omega were attributable primarily to differences in leaf boundary layer conductance among the cultivars. Plants of each cultivar that were 40% defoliated maintained sap flows comparable to pretreatment plants, but expected compensatory increases in g _s were not consistently observed. Despite their contrasting crown morphologies and hydraulic architecture, the three cultivars shared common relationships between water use and hydraulic architectural traits. Received: 17 February 1999 / Accepted: 28 July 1999     

Low conductances for CO2 diffusion from stomata to the sites of carboxylation in leaves of woody species

Concurrent measurements of leaf gas exchange and on-line ¹³C discrimination were used to evaluate the CO₂ conductance to diffusion from the stomatal cavity to the sites of carboxylation within the chloroplast (internal conductance; g_i). When photon irradiance was varied it appeared that g_i and/or the discrimination accompanying carboxylation also varied. Despite this problem, g_i, was estimated for leaves of peach (Prunus persica), grapefruit (Citrus paradisi), lemon (C. limon) and macadamia (Macadamia integrifolia) at saturating photon irradiance. Estimates for leaves of C. paradisi, C. limon and M. integrifolia were considerably lower than those previously reported for well-nourished herbaceous plants and ranged from 1.1 to2.2μmol CO₂ m^?2 s^?1 Pa^?1, whilst P. persica had a mean value of 3.5 μmol CO₂ m^?2 s^?1 Pa^?1. At an ambient CO₂ partial pressure of 33Pa, estimates of chloroplastic partial pressure of CO₂ (C_c) using measurements of CO₂ assimilation rate (A) and calculated values of g_i, and of partial pressure of CO₂ in the stomatal cavity (C_st) were as low as 11.2 Pa for C. limon and as high as 17.8Pa for peach. In vivo maximum rubisco activities (V_max) were also determined from estimates of C_c. This calculation showed that for a given leaf nitrogen concentration (area basis) C. paradisi and C. limon leaves had a lower V_max than P. persica, with C. paradisi and C. limon estimated to have only 10% of leaf nitrogen present as rubisco. Therefore, low CO₂ assimilation rates despite high leaf nitrogen concentrations in leaves of the evergreen species examined were explained not only by a low C_c but also by a relatively low proportion of leaf nitrogen being used for photosynthesis. We also show that simple one-dimensional equations describing the relationship between leaf internal conductance from stomatal cavities to the sites of carboxylation and carbon isotope discrimination (Δ) can lead to errors in the estimate of g_i. Potential effects of heterogeneity in stomatal aperture on carbon isotope discrimination may be particularly important and may lead to a dependence of g_i upon CO₂ assimilation rate. It is shown that for any concurrent measurement of A and Δ, the estimate of C_c is an overestimate of the correct photosynthetic capacity-weighted value, but this error is probably less than 1.0 Pa.     

Variations in photosynthetic rate and associated parameters with age of oil palm leaves under irrigation

Net photosynthetic rate (P _N), transpiration rate (E), and stomatal conductance (g _s) in an adult oil palm (Elaeis guineensis) canopy were highest in the 9^th leaf and progressively declined with leaf age. Larger leaf area (LA) and leaf dry mass (LDM) were recorded in middle leaves. P _N showed a significant positive correlation with g _s and a negative relationship with leaf mass per area (ALM). The oil palm leaf remains photosynthetically active for a longer time in the canopy which contributes significantly to larger dry matter production in general and greater fresh fruit bunch yields in particular.     

Direct and acclimatory responses of stomatal conductance to elevated carbon dioxide in four herbaceous crop species in the field

In order to separate the net effect of growth at elevated [CO₂] on stomatal conductance (g_s) into direct and acclimatory responses, mid‐day values of g_s were measured for plants grown in field plots in open‐topped chambers at the current ambient [CO₂], which averaged 350 μmol mol^?1 in the daytime, and at ambient + 350 μmol mol^?1[CO₂] for winter wheat, winter barley, potato and sorghum. The acclimatory response was determined by comparing g_s measured at 700 μmol mol^?1[CO₂] for plants grown at the two [CO₂]. The direct effect of increasing [CO₂] from 350 to 700 μmol mol^?1 was determined for plants grown at the lower concentration. Photosynthetic rates were measured concurrently with g_s. For all species, growth at the higher [CO₂] significantly reduced g_s measured at 700 μmol mol^?1[CO₂]. The reduction in g_s caused by growth at the higher [CO₂] was larger for all species on days with low leaf to air water vapour pressure difference for a given temperature, which coincided with highest conductances and also the smallest direct effects of increased [CO₂] on conductance. For barley, there was no other evidence for stomatal acclimation, despite consistent down‐regulation of photosynthetic rate in plants grown at the higher [CO₂]. In wheat and potato, in addition to the vapour pressure difference interaction, the magnitude of stomatal acclimation varied directly in proportion to the magnitude of down‐regulation of photosynthetic rate through the season. In sorghum, g_s consistently exhibited acclimation, but there was no down‐regulation of photosynthetic rate. In none of the species except barley was the direct effect the larger component of the net reduction in g_s when averaged over measurement dates. The net effect of growth at elevated [CO₂] on mid‐day g_s resulted from unique combinations of direct and acclimatory responses in the various species.     

Controls of Evapotranspiration and CO2 Fluxes from Scots Pine by Surface Conductance and Abiotic Factors

Evapotranspiration (E) and CO₂ flux (F_c) in the growing season of an unusual dry year were measured continuously over a Scots pine forest in eastern Finland, by eddy covariance techniques. The aims were to gain an understanding of their biological and environmental control processes. As a result, there were obvious diurnal and seasonal changes in E, F_c, surface conductance (g_c), and decoupling coefficient (Ω), showing similar trends to those in radiation (PAR) and vapour pressure deficit (δ). The maximum mean daily values (24-h average) for E, F_c, g_c, and Ω were 1.78 mmol m⁻² s⁻¹, −11.18 µmol m⁻² s⁻¹, 6.27 mm s⁻¹, and 0.31, respectively, with seasonal averages of 0.71 mmol m⁻² s⁻¹, −4.61 µmol m⁻² s⁻¹, 3.3 mm s⁻¹, and 0.16. E and F_c were controlled by combined biological and environmental variables. There was curvilinear dependence of E on g_c and F_c on g_c. Among the environmental variables, PAR was the most important factor having a positive linear relationship to E and curvilinear relationship to F_c, while vapour pressure deficit was the most important environmental factor affecting g_c. Water use efficiency was slightly higher in the dry season, with mean monthly values ranging from 6.67 to 7.48 μmol CO₂ (mmol H₂O)⁻¹ and a seasonal average of 7.06 μmol CO₂ (μmol H₂O)⁻¹. Low Ω and its close positive relationship with g_c indicate that evapotranspiration was sensitive to surface conductance. Mid summer drought reduced surface conductance and decoupling coefficient, suggesting a more biotic control of evapotranspiration and a physiological acclimation to dry air. Surface conductance remained low and constant under dry condition, supporting that a constant value of surface constant can be used for modelling transpiration under drought condition.     

Net CO2 assimilation of taro and cocoyam as affected by shading and leaf age

Taro and cocoyam were grown outdoors in either full sun or under 40% shade. Leaves were tagged as they emerged and the effect of leaf age on net CO₂ assimilation rate (A) was determined. The effects of shading on A, transpiration (E), stomatal conductance for CO₂ (g_c) and H₂O (g_s), and water use efficiency (WUE) were also determined for leaves of a single age for each species. The effect of leaf age on A was similar for both species. Net CO₂ assimilation rates increased as leaf age increased up to 28 days with the exception of a sharp decline in A for 21 day-old leaves which corresponded to unusually low temperatures during the period of leaf expansion. A generally decreased as leaves aged beyond 28 days. Cocoyam had higher A rates than taro. Leaves of shade-grown plants had higher rates of A and E for both species at photosynthetic photon flux densities (PPFD) up to 1600 mol s^–1 m^–2. Shade-grown leaves of cocoyam had greater leaf dry weights per area (LW/A) and a trend toward higher g_c and g_s than sun-grown leaves. Shade leaves of taro had greater g_c and g₃ rates than sun-grown leaves. The data suggest that taro and cocoyam are highly adapted to moderate shade conditions.     

Physiological divergences between two rhizomatous grasses from a desertification steppe,North China

The inter-and intra-specific physiological differences, e.g. rates of net photosynthesis (P _N) and transpiration (E), stomatal conductance (g _s), and water use efficiency (WUE), were compared between two grasses, Calamagrostis epigeios (L.) Roth. and Psammochloa villosa (Trin.) Bor., and between their leaf types in a desertification steppe in North China. The two species had a similar habitat, but differed in leaf area and rhizome depth. Leaf P _N, E, and g _s for P. villosa were significantly greater than those for C. epigeios in the growing season, but WUE for the former species was only 50 and 80 % of that for the latter one in dry and rainy seasons, respectively. In general, leaf P _N, E, g _s, and WUE for both vegetative and reproductive shoots of the two species exhibited little variations between leaf types or with leaf age, even though there were some remarkable differences between dry and rainy seasons. The mean leaf P _N and E in reproductive shoots of P. villosa were significantly lower than those in its vegetative shoots in rainy season, while these differences were much smaller for those of C. epigeios. P. villosa with deeper rhizome roots has relative higher leaf P _N, E, and g _s, but a smaller WUE in the arid desertification steppe region.     

Photosynthesis,transpiration, and water use efficiency of <Emphasis Type="Italic">Leymus dasystachys</Emphasis> on the Hunshandake desert

Net photosynthetic rate (P _N), transpiration rate (E), and stomatal conductance (g _s) declined from upper leaves to the lower ones during dry and rainy seasons, indicating that long-term carbon budget should take into account P _N variations for different leaf types. Relatively greater P _N in the dry season suggested that this species is more able to maintain higher P _N under drought, but the relatively higher E in the dry season might reduce water use efficiency (P _N/E) for the species. Significant correlations between P _N and g _s indicated that g _s may be the critical factor for P _N variability in the desert region.