Transpiration and canopy conductance in a pristine broad-leaved forest of Nothofagus: an analysis of xylem sap flow and eddy correlation measurements

Summary Tree transpiration was determined by xylem sap flow and eddy correlation measurements in a temperate broad-leaved forest of Nothofagus in New Zealand (tree height: up to 36 m, one-sided leaf area index: 7). Measurements were carried out on a plot which had similar stem circumference and basal area per ground area as the stand. Plot sap flux density agreed with tree canopy transpiration rate determined by the difference between above-canopy eddy correlation and forest floor lysimeter evaporation measurements. Daily sap flux varied by an order of magnitude among trees (2 to 87 kg day^–1 tree^–1). Over 50% of plot sap flux density originated from 3 of 14 trees which emerged 2 to 5 m above the canopy. Maximum tree transpiration rate was significantly correlated with tree height, stem sapwood area, and stem circumference. Use of water stored in the trees was minimal. It is estimated that during growth and crown development, Nothofagus allocates about 0.06 m of circumference of main tree trunk or 0.01 m² of sapwood per kg of water transpired over one hour.Maximum total conductance for water vapour transfer (including canopy and aerodynamic conductance) of emergent trees, calculated from sap flux density and humidity measurements, was 9.5 mm s^–1 that is equivalent to 112 mmol m^–2 s^–1 at the scale of the leaf. Artificially illuminated shoots measured in the stand with gas exchange chambers had maximum stomatal conductances of 280 mmol m^–2 s^–1 at the top and 150 mmol m^–2 s^–1 at the bottom of the canopy. The difference between canopy and leaf-level measurements is discussed with respect to effects of transpiration on humidity within the canopy. Maximum total conductance was significantly correlated with leaf nitrogen content. Mean carbon isotope ratio was –27.76±0.27 (average ±s.e.) indicating a moist environment. The effects of interactions between the canopy and the atmosphere on forest water use dynamics are shown by a fourfold variation in coupling of the tree canopy air saturation deficit to that of the overhead atmosphere on a typical fine day due to changes in stomatal conductance.This paper is dedicated to Prof. Dr. O.L. Lange on the occasion of his 65th birthday     

Water relations of stem succulent trees in north-central Baja California

Summary Water relations of several stem succulent trees were measured in north-central Baja California in comparisons to other growth forms in the same habitat. Our research concentrated on three stem succulent species (Idria collumnaris, Pachycormus discolor and Bursera microphylla) each with a different succulent stem morphology. The stem succulent trees had 1 to 4 kg H₂O/m³ of trunk while the other trees and shrubs in the same habitat had 0.6 to 0.8 kg H₂O/m³. The diurnal and seasonal variation in leaf water potential was small for the stem succulent species in comparison to deciduous and evergreen species as a consequence of the stem-water, buffering capacity. In addition, the leaf conductance of the stem succulent species was low (60 mmol m^–2 s^–1) and yet, the leaf conductance decreased through the day similar to adjacent evergreen and deciduous species. The leaves of the stem succulent trees lost turgor at low saturated water deficits (0.06 to 0.14), had comparatively high osmotic potentials, and high values of elastic modulus in comparison to adjacent evergreen and deciduous species. The stem acts as an important buffering mechanism allowing for the maintenance of leaf turgor in these stem succulent trees. The low transpiration rates of the stem succulent trees may be a mechanism to minimize leaf saturated water deficit and extend leaf longevity.     

Water relations of indigenous versus exotic tree species,growing at the same site in a tropical montane forest in southern Ethiopia

The objective of the study was to compare the water relations of two indigenous [Podocarpus falcatus (Thunb.) Endl., Croton macrostachys Hochst. ex. Del.] and two exotic tree species (Eucalyptus globulus Labille., Cupressus lusitanica Miller) growing in the same location in the montane Munessa State Forest, southern Ethiopia. Stem flow was measured with Granier type thermal dissipation probes. Sap flux, normalized per unit sapwood area, and the total sapwood areas of the particular trees were used to estimate daily transpiration. Maximum daily transpiration values (60 kg water) were recorded for Croton when at full foliage. After shedding most of its leaves in the dry season transpiration was reduced to 8 kg per day. Eucalyptus had the next highest transpiration (55 kg), in this case at the peak of the dry season. It transpired 4–5 times more than Podocarpus and Cupressus trees of similar size. Maximum stem flux density was tree-size dependent only in Croton. Diurnal patterns of stem flux indicated that Croton, Eucalyptus and Podocarpus, in contrast to Cupressus, responded more directly to light than to atmospheric water pressure deficit. At high VPD (>1.0 kPa) stem flux reached a plateau in Croton and Podocarpus indicating stomatal limitation. Per unit leaf area Croton had the highest and Podocarpus and Cupressus the lowest daily transpiration rates. In summary, the pioneer tree Croton had the lowest and Podocarpus the highest water use efficiency. The contribution of the study to the understanding of the role of each tree species in the hydrology of the natural forest and the plantations is discussed.     

A comparison of sap flux and water relations of leaves of various isolated trees with special reference to foundation movement in clay soil

Diurnal variation in sap flux (S) through stems of six trees, two each of Ulmus procera SALISB., Melaleuca styphelioides SM. and Prunus cerasifera EHRH. ‘Nigra’ (referred to hereafter by their generic names), were estimated from measurements of heat pulse velocities. Leaf water potential (ψ), stomatal conductance (g _s ) and transpiration from leaves (T) of all replicate trees were measured at 1300–1500h, once during the summer. On two separate occasions measurements were made of S, ψ, (g _s ) and T for one each of Ulmus and Melaleuca trees to study diurnal variations in these parameters. A 12×12 m² area around each tree was kept covered to simulate the condition of trees growing on pavements adjacent to residential properties. Sap flux for these tree species was in the order Melaleuca>Ulmus>Prunus. It is suggested that the smaller canopy and sapwood area in Prunus compared to the other two species is responsible for lower water potential and lower transpiration rate than the other species. Detailed analysis of the diurnal variation in sap flux and water relation of leaves of Melaleuca and Ulmus indicated sap flux of Melaleuca to be greater than that of Ulmus at the same transpiration rate per unit leaf area although the sapwood area of the two species was marginally different. This may have been due either to the difference in canopy conductance or in leaf area between the two species. With the assumption that sap flux closely resembles the rate of soil water extraction for both species, results indicate that Melaleuca is likely to extract soil water at a higher rate than Ulmus and hence is capable of causing greater shrinkage and soil movement than Ulmus.     

Effect of fruiting on carbon budgets of apple tree canopies

Summary Carbon budgets were calculated from net photosynthesis and dark respiration measurements for canopies of field-grown, 3-year-old apple trees (Malus domestica Borkh.) with maximum leaf areas of 5.4 m² in a temperature-controlled Perspex tree chamber, measured in situ over 2 years (July 1988 to October 1990) by computerized infrared gas analysis using a dedicated interface and software. Net photosynthesis (Pn) and carbon assimilation per leaf area peaked at respectively 8.3 and 7.7 mol CO₂ m^–2 s^–1 in April. Net photosynthesis (Pn) and dark respiration (Rd) per tree peaked at 3.6 g CO₂ tree^–1 h^–1 (Pn) and 1.2 g CO₂ tree^–1 h^–1 (Rd), equivalent to 4.2 mol CO₂ (Pn) and 1.4 mol CO₂ (Rd) m^–2 s^–1 with maximum carbon gain per tree in August and maximum dark respiration per tree in October 1988 and 1989. In May 1990, a tree was deblossomed. Pn (per tree) of the fruiting apple tree canopy exceeded that of the non-fruiting tree by 2–2.5 fold from June to August 1990, attributed to reduced photorespiration (RI), and resulting in a 2-fold carbon gain of the fruiting over the non-fruiting tree. Dark respiration of the fruiting tree canopy progressively exceeded, with increasing sink strength of the fruit, by 51% (June–August), 1.4-fold (September) and 2-fold (October) that of the non-fruiting tree due to leaf (i. e. not fruit) respiration to provide energy (a) to produce and maintain the fruit on the tree and (b) thereafter to facilitate the later carbohydrate translocation into the woody perennial parts of the tree. The fruiting tree reached its optium carbon budget 2–4 weeks earlier (August) then the non-fruiting tree (September 1990). In the winter, the trunk respired 2–100 g CO₂ month^–1 tree^–1. These data represent the first long-term examination of the effect of fruiting without fruit removal which shows increased dark respiration and with the increase progressing as the fruit developed.     

Effects of xylem sap flow on carbon dioxide efflux from stems of birch (Betula pendula Roth)

The effect of xylem sap flow in stems of mature Betula pendula Roth on radial CO₂ efflux was studied from April to October 2001. Temperature-controlled respiration cuvettes allowed measurements of CO₂ efflux without interference from temperature gradients between stem surface and sapwood. Variations of sap flow in different stem sectors, and in a given sector at different heights were analysed. Daytime reduction of CO₂ efflux caused by sap flow was expressed as the difference between gross and apparent CO₂ release. Gross CO₂ release was calculated from Arrhenius-equations derived from night-time data records of the same day, which were free from interference by sap flow. In mid-July, daytime reductions of CO₂ efflux reached 1.8–3.9 μmol CO₂ m⁻² g⁻¹ xylem sap transpired. Assuming tree-specific maximum transpiration rates of 30 kg H₂O d⁻¹ this is up to 40% of gross CO₂ release. In relation to photosynthetic CO₂ fixation the endogenous supply of dissolved CO₂ to the leaves acccounted for 0.5–3.7%. This study indicates a negative correlation between sap flow velocity and radial CO₂ efflux from B. pendula stems. Periods of unbalanced CO₂ partial pressures between aqueous and gaseous pathways during increase and decrease of sap flow seem to affect gaseous CO₂ release through lenticels. It is concluded that CO₂ efflux rates are not simply equivalent to respiration rates because of the interference of aqueous CO₂ transport by xylem sap flow in the wood-body of trees.     

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     

Transpiration and root water uptake by olive trees

While the cultivated olive tree (Olea europaea L.) is known to be sclerophyllous and effective at tolerating drought, little is known of its short-term water-use dynamics for most studies have been based on longer-term, water-balance information. We present here, for the first time, heat-pulse measurements of the sap flux measured not only within the semi-trunk of an olive tree, but also within a root excavated close to the stump. One tree in the olive grove near Seville in Spain had regularly received basin irrigation during the summer, whereas the other, growing on this deep silt loam, had been without water for over 3 months. Following a flood irrigation of 730 L to a dyked area around the tree, the regularly-irrigated olive maintained a transpiration rate of 1.65 mm³ mm^–2 d^–1, on a leaf area basis, for only 3 days following the irrigation. This rate was maintained for a total consumption of 110 L. It then began again to limit its rate of water use with transpiration falling below that predicted for well-watered conditions by the Penman-Monteith equation. The flow of sap in the near-surface root dropped concomitantly. Meanwhile the unirrigated tree was using water at just 0.78 mm d^–1. Yet following an irrigation of 870 L it only lifted its consumption to 1.12 mm d^–1, on a leaf area basis. Neither did it recover its leaf water potential following this wetting because of an inability to refill cavitated vessels. These data again show olive to be a parsimonious and cautious consumer of soil water.     

Regulation of xylem sap flow in an evergreen, a semi-deciduous, and a deciduous Meliaceae species from the Amazon

The significance of phenological characteristics, stomatal conductance of the leaves, and stem water storage fluctuations for the regulation of xylem sap flow in an evergreen (Carapa guianensis Aubl.), in a semi-deciduous (Swietenia macrophylla King), and in a deciduous (Cedrela odorata L.) Meliaceae species was studied in a 7-year-old plantation near Manaus, Brazil. The study responds to the increasing demand for knowledge on the water relations of highly exploited timber trees of the Amazon. Xylem sap flow measurements indicated that the daily sap flow of Carapa (3.8 l day^-1 tree^-1 to 16.4 l day^-1 tree^-1) exceeded the daily sap flow of Swietenia (2.4 l day^-1 tree^-1 to 7.0 l day^-1 tree^-1) and Cedrela (1.6 l day^-1 tree^-1 to 11.6 l day^-1 tree^-1) during the entire year, although the highest flux densities were measured in Cedrela. The decrease in xylem sap flow observed in periods with low soil water potentials and high atmospheric vapor saturation deficits was more pronounced in the deciduous (Cedrela) and semi-deciduous species (Swietenia) than the evergreen species (Carapa). Carapa, which has the highest daily sap flow, had the highest biomass and sapwood portion. The high flux densities measured in Cedrela most likely result from the large earlywood vessels in this species. The seasonal variation of xylem sap flow of the three species was correlated with the stomatal conductance of the leaves measured by infiltration experiments. Stem water storage fluctuations in Carapa and Swietenia were predominantly due to transpiration; in Cedrela it was predominantly due to evaporative water loss on the stem surface during dry periods.     

In situ measurement of fine root water absorption in three temperate tree species—Temporal variability and control by soil and atmospheric factors

Miniature heat balance-sap flow gauges were used to measure water flows in small-diameter roots (3–4 mm) in the undisturbed soil of a mature beech–oak–spruce mixed stand. By relating sap flow to the surface area of all branch fine roots distal to the gauge, we were able to calculate real time water uptake rates per root surface area (J_s) for individual fine root systems of 0.5–1.0 m in length. Study aims were (i) to quantify root water uptake of mature trees under field conditions with respect to average rates, and diurnal and seasonal changes of J_s, and (ii) to investigate the relationship between uptake and soil moisture θ, atmospheric saturation deficit D, and radiation I. On most days, water uptake followed the diurnal course of D with a mid-day peak and low night flow. Neighbouring roots of the same species differed up to 10-fold in their daily totals of J_s (<100–2000 g m⁻² d⁻¹) indicating a large spatial heterogeneity in uptake. Beech, oak and spruce roots revealed different seasonal patterns of water uptake although they were extracting water from the same soil volume. Multiple regression analyses on the influence of D, I and θ on root water uptake showed that D was the single most influential environmental factor in beech and oak (variable selection in 77% and 79% of the investigated roots), whereas D was less important in spruce roots (50% variable selection). A comparison of root water uptake with synchronous leaf transpiration (porometer data) indicated that average water fluxes per surface area in the beech and oak trees were about 2.5 and 5.5 times smaller on the uptake side (roots) than on the loss side (leaves) given that all branch roots <2 mm were equally participating in uptake. Beech fine roots showed maximal uptake rates on mid-summer days in the range of 48–205 g m⁻² h⁻¹ (i.e. 0.7–3.2 mmol m⁻² s⁻¹), oak of 12–160 g m⁻² h⁻¹ (0.2–2.5 mmol m⁻² s⁻¹). Maximal transpiration rates ranged from 3 to 5 and from 5 to 6 mmol m⁻² s⁻¹ for sun canopy leaves of beech and oak, respectively. We conclude that instantaneous rates of root water uptake in beech, oak and spruce trees are above all controlled by atmospheric factors. The effects of different root conductivities, soil moisture, and soil hydraulic properties become increasingly important if time spans longer than a week are considered.     

Sap flow as an indicator of transpiration and the water status of young apricot trees

The relationship between water loss via transpiration and stem sap flow in young apricot trees was studied under different environmental conditions and different levels of soil water status. The experiment was carried out in a greenhouse over a 2-week period (November 2–14, 1997) using three-year-old apricot trees (Prunus armeniaca cv. Búlida) growing in pots. Diurnal courses of leaf water potential, leaf conductance and leaf turgor potential also were recorded throughout the experiment. Data from four days of different enviromental conditions and soil water availability have been selected for analysis. On each of the selected days the leaf water potential and the mean transpiration rates were well correlated. The slope of the linear regression of this correlation, taken to indicate the total hydraulic resistance of the tree, confirmed an increasing hydraulic resistance under drought conditions. When the trees were not drought stressed the diurnal courses of sap flow and transpiration were very similar. However, when the trees were droughted, measured of sap flow slightly underestimated actual transpiration. Our heat-pulse measurements suggest the amount of readily available water stored in the stem and leaf tissues of young apricot trees is sufficient to sustain the peak transpiration rates for about 1 hour. This revised version was published online in June 2006 with corrections to the Cover Date.     

Contribution of vines to the evapotranspiration of a secondary forest in eastern Amazonia

The contribution of vines to the evapotranspiration (ET) of a secondary forest in eastern Amazonia was estimated based on field measurements of vine and tree transpiration, and seasonal changes in soil water content to 12 meters depth. Transpiration of vines and trees was measured with sapflow gauges placed around stems or branches. Total ET of the secondary forest was estimated as the sum of rainfall and reductions in soil moisture measured using Time Domain Reflectometry sensors installed in the walls of soil shafts. Our results suggest that vines transpire more than trees with stems of similar diameter, and with similar leaf crown exposure to sunlight. Trees experienced a smaller reduction in transpiration from the wet to the dry season than did vines. During the dry season, vines represented 8% (0.4 mm d^–1) of total secondary forest ET (5.4 mm d^–1), but they represented only 5.5% (0.5 m² ha^–1) of total secondary forest basal area (9.6 m² ha^–1). Considering that transpiration corresponds to 66–90% of forest ET, vines may contribute 9–12% to the transpiration of the forest. Hence, vine cutting, which is a commonly recommended management practice to favor the growth of tropical timber trees, may result in a proportionally larger reduction in evapotranspiration than in forest basal area.     

Time constant for water transport in loblolly pine trees estimated from time series of evaporative demand and stem sapflow

 The use of stem sap flow data to estimate diurnal whole-tree transpiration and canopy stomatal conductance depends critically upon knowledge of the time lag between transpiration and water flux through the stem. In this study, the time constant for water movement in stems of 12-year-old Pinus taeda L. individuals was estimated from analysis of time series data of stem water flux and canopy transpiration computed from mean daytime canopy conductance, and diurnal vapor pressure deficit and solar radiation measurements. Water uptake through stems was measured using a constant-heat sapflow probe. Canopy transpiration was correlated to stem uptake using a resistance-capacitance equation that incorporates a time constant parameter. A least-squares auto-regression determined the parameters of the resistance-capacitance equation. The time constants for ten loblolly pine trees averaged 48.0 (SE = 2.0) min and the time lag for the diurnal frequency averaged 47.0 (SE = 2.0) min. A direct-cross correlation analysis between canopy transpiration and sap flow time series showed maximum correlation at an approximately 30 min lag. Residuals (model-predicted minus actual stem flow data) increased with increasing soil moisture depletion. While the time constants did not vary significantly within the range of tree sizes studied, hydraulic resistance and capacitance terms were individually dependent on stem cross-sectional area: capacitance increased and resistance decreased with stem volume. This result may indicate an inverse adjustment of resistance and capacitance to maintain a similar time constant over the range of tree sizes studied.     

Gender specific patterns of carbon uptake and water use in a dominant riparian tree species exposed to a warming climate

Air temperatures in the arid western United States are predicted to increase over the next century. These increases will likely impact the distribution of plant species, particularly dioecious species that show a spatial segregation of the sexes across broad resource gradients. On the basis of spatial segregation patterns, we hypothesized that temperature increases will have a greater negative impact on female plants compared with co‐occurring male plants of dioecious species. This hypothesis was tested by examining the whole‐plant carbon and water relations of 10‐year‐old female (n = 18) and male (n = 13) Acer negundo Sarg. trees grown in a common garden in Salt Lake City, UT. The trees were established from cuttings collected where the growing season temperature averaged about 6.5 °C cooler than at the common garden. During May and June, stem sap flux (J_s) was similar between genders, but averaged 25% higher in males during the warmer months of July and August. Daytime canopy stomatal conductance (g_s) per unit leaf area was 12% higher in females in May : June, but was 11% higher in males in July : August. We combined measurements of sap flux–scaled transpiration with measurements of tree allometry and δ¹³C of leaf soluble sugars to estimate whole‐tree carbon assimilation (A_tree) and water use efficiency (WUE) (A_tree : E_tree). A_tree was similar between genders until late August when A_tree was 32% higher in male trees. A_tree : E_tree was on average 7% higher in females than in males during the growing season. Patterns of J_s, g_s, A_tree and A_tree : E_tree in the present study were in contrast to those previously reported for A. negundo genders under native growing season temperatures. Results suggest that the spatial segregation of the sexes could shift under global warming such that female plants lose their dominance in high‐resource habitats, and males increase their dominance in relatively lower‐resource habitats.     

Canopy transpiration in a chronosequence of Central Siberian pine forests

Tree transpiration was measured in 28, 67, 204 and 383‐y‐old uniform stands and in a multicohort stand (140–430 y) of Pinus sylvestris ssp. sibirica Lebed. in Central Siberia during August 1995. In addition transpiration of three codominant trees was monitored for two years in a 130‐y‐old stand. All stands established after fire. Leaf area index (LAI) ranged between 0.6 (28‐y‐old stand) and 1.6 for stands older than 67‐y. Stand xylem area at 1.3 m height increased from 4 cm² m^?2 (28‐y) to 11.5 cm² m^?2 (67‐y) and decreased again to 7 cm² m^?2 in old stands. Above‐ground living biomass increased from 1.5 kg dry weight m^?2 (28‐y) to 14 kg dry weight m^?2 (383‐y). Day‐to‐day variation of tree transpiration in summer was dependent on net radiation, vapour pressure deficit, and soil water stress. Tree‐to‐tree variation of xylem flux was small and increased with heterogeneity in canopy structure. Maximum rates of xylem flux density followed the course of net radiation from mid April when a constant level of maximum rates was reached until mid September when low temperatures and light strongly reduced flux density. Maximum sap flux density (60 g m^?2 s^?1) and canopy transpiration (1.5 mm d^?1) were reached in the 67‐y stand. Average canopy transpiration of all age classes was 0.72 ± 0.3 mm d^?1. Canopy transpiration (E) was not correlated with LAI but related to stand sapwood area SA (E = ? 0.02 + 1.15SA R²) which was determined by stand density and tree sapwood area.     

基于树干液流及涡动相关技术的葡萄冠层蒸腾及蒸散发特征研究

针对西北干旱区绿洲经济作物葡萄树冠层蒸腾及蒸散发特征的相关问题,在甘肃省敦煌市南湖绿洲开展无核白葡萄树液流速率及蒸散发观测试验,采用基于热平衡原理的包裹式茎流计,详细分析了典型生长季7—9月份葡萄树蒸腾耗水规律,使用"单位叶面积上的平均液流速率SF×叶面积指数LAI"的方法,实现了从单株到林分冠层蒸腾的尺度扩展,并通过与涡动相关技术所测蒸散发数据对比,详细研究了葡萄地冠层蒸腾及蒸散发规律。结果表明:典型生长季中葡萄树液流速率日变化为单峰型曲线,日均耗水量从2.76 kg到10 kg不等,胸径越大的葡萄树日均耗水量越大;冠层蒸腾及蒸散发日变化曲线亦为单峰型,白天8:00—12:00与17:00—20:00期间,葡萄冠层蒸腾与蒸散发曲线均比较吻合,该时间段葡萄地蒸散发绝大部分来源于葡萄冠层蒸腾,而12:00—17:00之间由于午后太阳辐射强烈土壤蒸发量增加,葡萄蒸散发大于冠层蒸腾;典型生长季3个月中,葡萄冠层蒸腾量的变化范围在1.88—8.12 mm/d之间,日均冠层蒸腾量为6.12 mm/d,蒸散发在1.74 mm/d至10.78 mm/d之间,日均蒸散发量为7.13 mm/d;日均土壤蒸发量约为1.01 mm/d,只占总蒸散发量的14.2%,日均冠层蒸腾占日均蒸散发的比重达到85.8%,说明该生长阶段冠层蒸散发以作物蒸腾为主。     

Urban tree root systems and their survival near houses analyzed using ground penetrating radar and sap flow techniques

Root systems of two mature Field maple trees (Acer campestre L.) growing in both shaded and non-shaded sites, on clay soil in an urban environment, were analyzed by ground penetrating radar (GPR), light microscope and sap flow techniques. The ground surface above the root systems was covered by asphalt. However, a small piece of garden existed near the non-shaded tree, and root area of roots growing in this direction increased significantly, due to a presumed increase in available water and nutrients. However, no garden was present near the shaded tree, therefore roots remaining under the asphalt surface did not increase in area in any particular direction. Maximum rooting depth of shaded and exposed trees, as determined by GPR, was approximately 1.4 and 1.7 m, respectively. The trees utilized relatively large amounts of water for transpiration, i.e. 65–140 l per fine summer day and in average 10 m³ per growing season. However, transpiration expressed per root surface area (and/or whole root system enveloping area) was practically the same in both trees, i.e. 1 dm³ m^-2 d^-1 or almost 100 dm³ m^-2 per growing season. These figures represented about 50% of potential evapotranspiration when considering projected crown areas. Increased transpiration under long-term high evaporation demands may cause occasional local drying of soil around roots, associated with soil shrinking in clay, which can be followed by serious damage to buildings.     

The effect of fertilization on sap flux and canopy conductance in a Eucalyptus saligna experimental forest

Land devoted to plantation forestry (50 million ha) has been increasing worldwide and the genus Eucalyptus is a popular plantation species (14 million ha) for its rapid growth and ability to grow well on a wide range of sites. Fertilization is a common silvicultural tool to improve tree growth with potential effects on stand water use, but the relationship between wood growth and water use in response to fertilization remains poorly quantified. Our objectives in this study were to determine the extent, timing and longevity of fertilization effects on water use and wood growth in a non‐water limited Eucalyptus saligna experimental forest near Hilo, HI. We evaluated the short‐ and long‐term effects of fertilization on water use by measuring sap flux per unit sapwood area, canopy conductance, transpiration per unit leaf area and water‐use efficiency in control and fertilized stands. Short‐term effects were assessed by comparing sap flux before and after fertilizer application. Long‐term effects were assessed by comparing control plots and plots that had received nutrient additions for 5 years. For the short‐term response, total water use in fertilized plots increased from 265 to 487 mm yr^?1 during the 5 months following fertilization. The increase was driven by an increase in stand leaf area accompanied by an increase in sap flux per unit sapwood area. Sap flux per unit leaf area and canopy conductance did not differ during the 5 months following fertilizer additions. For the last 2 months of our short‐term measurements, fertilized trees used less water per unit carbon gain (361 compared with 751 kg H₂O kg C^?1 in control stands). Trees with 5 years of fertilization also used significantly more water than controls (401 vs. 302 mm yr^?1) because of greater leaf area in the fertilized stands. Sap flux per unit sapwood area, sap flux per unit leaf area, and canopy conductance did not differ between control and fertilized trees in the long‐term plots. In contrast to the short‐term response, the long‐term response of water use per unit wood growth was not significant. Overall, fertilization of E. saligna at our site increased stand water use by increasing leaf area. Fertilized trees grew more wood and used more water, but fertilization did not change wood growth per unit water use.     

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.     

Leaf Water Relations and Sapflow in Eastern Cottonwood (Populus deltoides Bartr.) Trees Planted for Phytoremediation of a Groundwater Pollutant

Plants that remediate groundwater pollutants may offer a feasible alternative to the traditional and more expensive practices. Because its success depends on water use, this approach requires a complete understanding of species-specific transpiration patterns. The objectives of this study were (1) to quantify tree and stand-level transpiration in two age classes (whips and 1-year-old seedlings) of eastern cottonwoods (Populus deltoides Bartr.), and (2) to determine climatic and physiological driving variables at the Carswell Air Force Base in central Texas, USA. Trichloroethylene (TCE) was detected in shallow (2 to 3 m) groundwater in the early 1980s. Cottonwood whips and 1-year-old potted seedlings were planted in two separate 0.15-ha plantations in spring 1996. Sapflow gauges determined sapflow on 14 to 16 trees in May, June, July, August, and October 1997. Without adjusting for differences in tree size, sapflow rates were greater for 1-year-old trees than whips (peak values were 0.75 and 0.53 kg hr^-1 tree^-1, respectively). When adjusted for tree size, the pattern reversed, with whips having significantly greater sapflow rates than 1-year-old trees (peak values were 0.053 and 0.045 kg cm^-2 hr^-1, respectively). Temporal variation (diurnal and seasonal) in sapflow rates was principally related to VPD, solar radiation, and leaf conductance. Extrapolating to the stand and across the growing season, the plantations transpired ~25 cm of water. Early attainment of high levels of transpiration indicates that the stands will transpire considerably more water as leaf area and root exploitation increases with stand development.