Effects of phosphorus deficiency on the photosynthesis and respiration of leaves of sugar beet

Phosphorus deficiency was induced in sugar beet plants (Beta vulgaris L. var. F5855441), cultured hydroponically under standardized environmental conditions, by removal of phosphorus from the nutrient supply at the ten leaf stage 28 days after germination. CO₂ and water vapor exchange rates of individual attached leaves were determined at intervals after P cutoff. Leaves grown with an adequate nutrient supply attained net rates of photosynthetic CO₂ fixation of 125 ng CO₂ cm⁻² sec⁻¹ at saturating irradiance, 25 C, and an ambient CO₂ concentration of about 250 μl l⁻¹. After P cutoff, leaf phosphorus concentrations decreased as did net rates of photosynthetic CO₂ uptake, photorespiratory evolution of CO₂ into CO₂-free air, and dark respiration, so that 30 days after cutoff these rates were about one-third of the control rates. The decrease in photosynthetic rates during the first 15 days after cutoff was associated with increased mesophyll resistance (r_m) which increased from 2.4 to 4.9 sec cm⁻¹, while from 15 to 30 days there was an increase in leaf (mainly stomatal) diffusion resistance (r_l′) from 0.3 to 0.9 sec cm⁻¹, as well as further increases in r_m to 8.5 sec cm⁻¹. Leaf diffusion resistance (r_l′) was increased greatly by low P at low but not at high irradiance, r_l′ for plants at low P reaching values as high as 9 sec cm⁻¹.     

Leaf diffusion resistance, illuminance, and transpiration

Stepwise increases in fluorescent illuminance, imposed as a single variable in a controlled environment, induced progressive stomatal opening in 8 plant species, as evidenced by a consistent decrease in leaf diffusion resistance (R_L), ranging from 15 to 70 sec cm⁻¹ in darkness to about 1 sec cm⁻¹ at approximately 40 kilolux. The minimum R_L values were the same for the upper and the lower epidermis, provided that stomatal density was adequate. Saturation illuminance was not achieved in any species; extrapolation indicates that 50 kilolux would bring about full stomatal opening (R_L ≤ 0.1 sec cm⁻¹).

In 4 species, reasonable agreement was obtained in a controlled environment between transpiration as measured by weight loss and that calculated from determination of (a) the difference in water vapor density from leaf to air, (b) the boundary layer resistance, and (c) the leaf diffusion resistance. This result confirms the physical validity of the resistance measurement procedure.

     

Water Relations and Photosynthesis of a Desert CAM Plant, Agave deserti

The water relations and photosynthesis of Agave deserti Engelm., a plant exhibiting Crassulacean acid metabolism, were measured in the Colorado desert. Although no natural stomatal opening of A. deserti occurred in the summer of 1975, it could be induced by watering. The resistance for water vapor diffusion from a leaf (R_WV) became less than 20 sec cm⁻¹ when the soil water potential at 10 cm became greater than −3 bars, as would occur after a 7-mm rainfall. As a consequence of its shallow root system (mean depth of 8 cm), A. deserti responded rapidly to the infrequent rains, and the succulent nature of its leaves allowed stomatal opening to continue for up to 8 days after the soil became drier than the plant. When the leaf temperature at night was increased from 5 to 20 C, R_WV increased 5-fold, emphasizing the importance of cool nighttime temperatures for gas exchange by this plant. Although most CO₂ uptake occurred at night, a secondary light-dependent rise in CO₂ influx generally occurred after dawn. The transpiration ratio (mass of water transpired/mass of CO₂ fixed) had extremely low values of 18 for a winter day, and approximately 25 for an entire year.     

Detrimental effect of rust infection on the water relations of bean

Bean plants (Phaseolus vulgaris L.) infected with the rust Uromyces phaseoli became unusually susceptible to drought as sporulation occurred. Under the conditions used (1,300 ft-c, 27 C, and 55% relative humidity) such plants wilted at soil water potentials greater than −1 bar, whereas healthy plants did not wilt until the soil water potential fell below −3.4 bars. Determinations of leaf water and osmotic potentials showed that an alteration in leaf osmotic potential was not responsible for the wilting of diseased plants. When diffusive resistance was measured as a function of decreasing leaf water content, the resistance of healthy leaves increased to 50 sec cm⁻¹ by the time relative water content decreased to 70%, whereas the resistance of diseased leaves remained less than 8 sec cm⁻¹ down to 50% relative water content. Apparently, water vapor loss through cuticle damaged by the sporulation process, together with the reduction in root to shoot ratio which occurs in diseased plants, upset the water economy of the diseased plant under mild drought conditions.     

RNA Synthesis in Spring and Winter Wheat during Cold Acclimation

The factors responsible for the low transpiration rates of citrus were investigated. Leaf resistance to water vapor exchange by orange seedlings (Citrus sinensis L. cv. Koethen) including a substantial boundary layer resistance, was as low as 1 s cm⁻¹ in humid air. Leaf resistance of well watered plants increased to values as large as 5 s cm⁻¹ when the difference in absolute humidity between leaf and air was increased. Leaf resistance was only slightly influenced by temperature between 20 and 30°C providing the humidity difference between leaf and air was kept constant. Leaf resistance increased when leaf temperature was increased between 20 and 30°C when the absolute humidity external to the leaf was kept constant. Increased humidity differences resulted in greater increases in leaf resistance during initial experiments than when the experiments were repeated with the same leaves indicating acclimation by the plant. It was concluded that the effects of humidity differences on leaf resistance are partially responsible for the low transpiration rates of citrus.     

Developmental history affects the susceptibility of spinach leaves to in vivo low temperature photoinhibition

Room temperature chlorophyll a fluorescence was used to determine the effects of developmental history, developmental stage, and leaf age on susceptibility of spinach to in vivo low temperature (5°C) induced photoinhibition. Spinach (Spinacia oleracea cv Savoy) leaves expanded at cold hardening temperatures (5°C day/night), an irradiance of 250 micromoles per square meter per second of photosynthetic proton flux density, and a photoperiod of 16 hours were less sensitive than leaves expanded at nonhardening temperatures (16 or 25°C day/night) and the same irradiance and photoperiod. This differential sensitivity to low-temperature photoinhibition was observed at high (1200) but not lower (500 or 800 micromoles per square meter per second) irradiance treatment. In spite of a differential sensitivity to photoinhibition, both cold-hardened and nonhardened spinach exhibited similar recovery kinetics at either 20 or 5°C. Shifting plants grown at 16°C (day/night) to 5°C (day/night) for 12 days after full leaf expansion did not alter the sensitivity to photoinhibition at 5°C. Conversely, shifting plants grown at 5°C (day/night) to 16°C (day/night) for 12 days produced a sensitivity to photoinhibition at 5°C similar to control plants grown at 16°C. Thus, any resistance to low-temperature photoinhibition acquired during growth at 5°C was lost in 12 days at 16°C. We conclude that leaf developmental history, developmental stage, and leaf age contribute significantly to the in vivo photoinhibitory response of spinach. Thus, these characteristics must be defined clearly in studies of plant susceptibility to photoinhibition.     

MICROCLIMATIC EFFECTS ON WATER RELATIONS,LEAF TEMPERATURES,AND THE DISTRIBUTION OF HERACLEUM LANATUM AT HIGH ELEVATIONS

The small-scale distribution of an understory herb, Heracleum lanatum, was evaluated in terms of leaf temperature and water relations limitations due to a large leaf size (630 cm²). Diurnal variations in transpiration (4 to 60 mg m⁻² s⁻¹) were influenced by fluctuations in solar irradiance, wind speed, leaf temperature and stomatal conductance. Computer simulations indicated that leaf temperatures in a forest clearing would be > 12 C above air temperature, with maximum transpiration rates of 140 mg m⁻² s⁻¹, and daily water loss to be over 200% greater than values at natural understory locations. Simulations of nocturnal temperature relations indicated ~100 W m ⁻² less incident longwave irradiance in the forest clearing as compared to the understory (560 vs. 660 W m⁻² at 400 hr). This difference led to predicted leaf temperatures being as low as 6 C below air temperature in the forest clearing while measured leaf temperatures in the forest understory were within 1.5 C of air temperature throughout the night. Furthermore, minimum air temperatures were at or below 6 C on 36% of the nights during the summer growth period indicating that in open areas leaves of H. lanatum would frequently be below 0 C and subject to possible freeze damage. Heracleum lanatum may be more abundant in the shaded understory of the subalpine forest because exposure in open environments would result in high leaf temperatures and increased transpirational water loss during the day, as well as low leaf temperatures with the possibility of freeze damage at night.     

The effect of root temperature on rose plants in relation to air temperature

Rose plants (Rosa hybrida ‘Sonia’=‘Sweet Promise’) were grown in heated (minimum night temperature 17°C), and unheated greenhouses with or without root heating to 21°C. These trials covered 6 growth cycles extending over two winter seasons. In the heated greenhouse, root heating did not increase yield, flower quality or plant development. In the unheated greenhouse, root-heated plants grew as well as those in the air-heated greenhouse as long as the air temperature did not fall below 6°C. When minimum night temperatures fell below 6°C, growth, yield and quality were reduced, irrespective of root temperature. Daytime plant water relations were studied in plants growing at 6 different root temperatures in the unheated greenhouse. Leaf resistance to water diffusion was lowest at optimal root temperature. Total leaf water potential was not significantly affected by root temperature.     

Effects of magnesium deficiency on the photosynthesis and respiration of leaves of sugar beet

The effects of Mg deficiency on the photosynthesis and respiration of sugar beets (Beta vulgaris L. cv. F58-554H1) were studied by withholding Mg from the culture solution and by following changes in CO₂ and water vapor exchange of attached leaves. Leaf blade Mg concentration decreased from about 1200 to less than 200 meq kg⁻¹ dry matter without change in the rate of photosynthetic CO₂ uptake per unit leaf area, while from 200 to 50 meq kg⁻¹ the rate decreased to one-third. Rates of photorespiratory evolution of CO₂ into CO₂-free air responded to Mg like those of photosynthetic CO₂ uptake, the rates decreasing to one-half, below 200 meq kg⁻¹. Respiratory CO₂ evolution in the dark increased almost 2-fold in low Mg leaves. Magnesium deficiency had less effect on leaf (mainly stomatal) diffusion resistance (r₁) than on mesophyll resistance (r_m); in Mg-deficient plants r_m increased from 2.9 to 7.1 sec cm⁻¹, whereas r₁ became significantly greater than the control value only in the most severe instances of Mg deficiency.     

Direct relation between growth and frost hardening in cabbage leaves

Potted cabbage plants were grown in growth chambers at 25° day and 15° night and hardened successively at 5, 0, and −3°. Leaf growth was determined by measuring leaf area, hardiness by freezing at a series of temperatures and determining percent survival. Leaf growth increased progessively with leaf number, reaching a maximum rate of growth and final area in the tenth and eleventh leaves when the plants become potbound. Leaf growth continued at hardening temperatures of 5 or 0°, the Q₁₀ being 2.0 to 2.5. Ability to harden also increased with leaf number, paralleling the growth rate of the leaves just before hardening as well as the growth rate and the total growth during hardening. The above results were similar whether prolonged (several weeks) or brief (24 hr) hardening was utilized.     

Effects of environment,seedling age,and seed source on leaf resistance of three species of Chamaecyparis and Tsuga chinensis

Summary The objectives of this study were to determine how stomata of Chamaecyparis spp. react to environmental changes and to determine in what ways leaf resistance patterns may have adaptive value for these confers. Leaf resistances were measured of Chamaecyparis taiwanensis, C. formosensis and C. lawsoniana seedlings in a forest nursery, and of saplings of the first two species and Tsuga chinensis growing in natural forest and clearcuts. Light, temperature, humidity, and sometimes xylem pressure potential were measured concurrently.In the nursery, C. lawsoniana, the species from the driest climate, had the lowest resistance, daily means for well-watered yearold plants being 2–5 s cm^-1. Leaf resistances of well-watered C. formosensis and C. taiwanensis from more humid habitats were two and three times greater. Leaf resistance was more sensitive to environment in those nursery populations of C. formosensis from habitats where a dry season is more severe. There were no clear patterns of variation within the other species. Resistance of scale leaves increased with seedling size and age. Primary leaves of C. formosensis had higher average resistance than its scale leaves, and were more responsive to changes in the environment.In the field, C. taiwanensis had higher resistance than C. formosensis. Leaf resistance of Tsuga chinesis was quite similar to that of C. formosensis. Resistance decreased from winter to spring except during a severe dry spell in March.Changes in leaf resistance were most consistently correlated with humidity, which often increased during the day as humid air rose from the lowlands. Stomata opened as humidity rose even when plant xylem pressure potentials were -15 to -23 bars. Stomatal reaction of Chamaecyparis spp. varies in ways apparently adaptive to their environment.     

The Effect of Leaf Water Potential, Leaf Temperature and Light Intensity on Leaf Diffusion Resistance and the Transpiration of Leaves of Malus sylvestris

The relationship between leaf resistance to water vapour diffusion and each of the factors leaf water potential, light intensity and leaf temperature was determined for leaves on seedling apple trees (Malus sylvestris Mill. cv. Granny Smith) in the laboratory. Leaf cuticular resistance was also determined and transpiration was measured on attached leaves for a range of conditions. Leaf resistance was shown to be independent of water potential until potential fell below — 19 bars after which leaf resistance increased rapidly. Exposure of leaves to CO₂-free air extended the range for which resistance was independent of water potential to — 30 bars. The light requirement for minimum leaf resistance was 10 to 20 W m^?2 and at light intensities exceeding these, leaf resistance was unaffected by light intensity. Optimum leaf temperature for minimum diffusion resistance was 23 ± 2°C. The rate of change measured in leaf resistance in leaves given a sudden change in leaf temperature increased as the magnitude of the temperature change increased. For a sudden change of 1°C in leaf temperature, diffusion resistance changed at a rate of 0.01 s cm^?1 min^?1 whilst for a 9°C leaf temperature change, diffusion resistance changed at a rate of 0.1 s cm^?1 min^?1. Cuticular resistance of these leaves was 125 s cm^?1 which is very high compared with resistances for open stomata of 1.5 to 4 s cm^?1 and 30 to 35 s cm^?1 for stomata closed in the dark. Transpiration was measured in attached apple leaves enclosed in a leaf chamber and exposed to a range of conditions of leaf temperature and ambient water vapour density. Peak transpiration of approximately 5 × 10^?6 g cm^?2 s^?1 occurred at a vapour density gradient from the leaf to the air of 12 to 14 g m^?3 after which transpiration declined due presumably to increased stomatal resistance. Leaves in CO₂-free air attained a peak transpiration of 11 × 10^?6 g cm^?2 s^?1 due to lower values of leaf resistance in CO₂ free air. Transpiration then declined in these leaves due to development of an internal leaf resistance (of up to 2 s cm^?1). The internal resistance was masked in leaves at normal CO₂ concentrations by the increase in stomatal resistance.     

LEAF RESISTANCE TO WATER VAPOR TRANSFER IN SUCCULENT PLANTS: EFFECT OF THERMOPERIOD

Leaf resistance (R_L) of Kalanchoe blossfeldiana to water vapor transfer was determined with a resistance hygrometer. The diurnal leaf-resistance change followed a normal pattern (i.e., low in light and higher in dark) when plants were pretreated with cool thermoperiods or with thermoperiods having little diurnal temperature fluctuation. Large diurnal temperature fluctuations (30-18, 26-15 C) resulted in apparent nocturnal stomatal opening. Nocturnal stomatal opening was more apparent than real since leaf-resistance measurements indicated day stomatal closing rather than complete night opening. Low nocturnal leaf resistances ( < 10 sec/cm) were not measured in the dark; however, resistances tended to decrease toward the end of the dark period indicating some degree of nocturnal stomatal opening. Leaf resistances were generally higher than those reported for nonsucculent plants. The data suggested that gaseous diffusion (Q) into or out of the leaves of K. blossfeldiana would be adequately described by an equation of the form, Q = D Δ e R_L⁻¹. There was little or no indication that physiological long days (15 min of 660 mμ light in the middle of a 16-hr dark period), which prevented flowering and reduced organic acid accumulation, significantly affected leaf resistance. It was concluded that the photoperiod response effects of dark CO₂ fixation were probably not due to leaf-resistance changes and, therefore, not due to stomatal aperture changes.     

Effects of day-to-day changes in root temperature on leaf conductance to water vapour and CO2 assimilation rates of Vigna unguiculata L. Walp.

Summary Leaf gas exchange of Vigna unguiculata was influenced by short-term (day-to-day) changes in soil temperature and the response depended upon the aerial environment. When aerial conditions were constant at 30° C leaf temperature, high air humidity and moderate quantum flux, CO₂ assimilation rate and leaf conductance increased with increases in soil temperature from 20 to 35° C, and this response was reversible. Decreases in CO₂ assimilation rate and leaf conductance were observed at root temperatures above 30° C when root temperatures were increased from 20° C to 40° C and when air humidity was decreased in steps during the day. In contrast, varying soil temperatures between 20 to 35° C had no influence on gas exchange when shoots were subjected to a wide range of temperatures during each day.The gain ratio A/E remained constant at different air humidities when root temperature was less than or equal to 30° C indicating optimal gas exchange regulation, but changed with humidity at higher root temperatures. Leaf conductance responded independently from leaf water potential which remained relatively constant during individual experiments.The results indicate that plant responses to high root temperatures may have relevance to plant performance in semi-arid environments. They also illustrate the importance of controlling soil temperatures when studying the responses of potted plants in controlled aerial environments.Dedicated to K.F. Springer     

Response of stomatal resistance and photosynthesis to night temperature in Populus deltoides

Summary Ramets from stem cuttings of three populations of Populus deltoides Bartr. from Wisconsin, Illinois, and Louisiana representing a latitudinal gradient were grown in pots outdoors at Urbana, Illinois and brought indoors for growth chamber studies. Leaf resistance and photosynthetic response to low night temperatures of 4° and 10° C were determined relative to 20° C controls for plants measured over one growing season. Plants from Louisiana, where nights are warm, reacted to cool nights of 4° and 10° C by opening their stomata slower upon illumination the following day than those from farther north where nights are cooler. The optimum night temperature for rate of opening was lower in the Wisconsin population than in populations from farther south. The Wisconsin population showed more ideal homeostasis of photosynthesis at different temperatures than the southern population which exhibited greater plasticity. No seasonal differences in these relationships were apparent other than at the time of leaf senescence.As plants approached senescence, which occurred earliest in the Wisconsin population, leaf resistance increased and photosynthesis declined, but stomata still retained their functional ability to respond to changes in night temperature. The change in leaf resistance, noted in the Wisconsin population, was related more to closure of lower-leaf surface stomata than upper. Only the Louisiana population had significantly more stomata on the lower than upper leaf surface.     

Resistance Analysis of Nocturnal Carbon Dioxide Uptake by a Crassulacean Acid Metabolism Succulent, Agave deserti

Nocturnal CO₂ uptake by a Crassulacean acid metabolism succulent, Agave deserti Engelm. (Agavaceae), was measured so that the resistance properties of the mesophyll chlorenchyma cells and their CO₂ concentrations could be determined. Two equivalents of acidity were produced at night per mole of CO₂ taken up. The nocturnal CO₂ uptake became light-saturated at 3.5 mEinsteins cm⁻² of photosynthetically active radiation (400-700 nm) incident during the preceding day; at least 46 Einsteins were required per mole of CO₂ fixed. Variations in the daytime leaf temperature between 20 and 37 C had little effect on nocturnal CO₂ uptake. After the first few hours in the dark, the leaf liquid phase CO₂ resistance (r^liq_CO2) and the CO₂ concentration in the chlorenchyma cells (cⁱ_CO2) both increased, the latter usually reaching the ambient external CO₂ level at the end of the dark period. Increasing the leaf surface temperature above 15 C at night markedly increased the stomatal resistance, r^liq_CO2, and cⁱ_CO2.

The minimum r^liq_CO2 at night was about 1.6 seconds cm⁻¹. Based on the ratio of chlorenchyma surface area to total leaf surface area of 82, this r^liq_CO2 corresponded to a minimum cellular resistance of approximately 130 seconds cm⁻¹, comparable to values for mesophyll cells of C₃ plants. The contribution of the carboxylation reaction and/or other biochemical steps to r^liq_CO2 may increase appreciably as the nighttime temperature shifts a few degrees from the optimum or after a few hours in the dark, both of which caused large increases in r^liq_CO2. This necessitates a large internal leaf area for CO₂ diffusion into the chlorenchyma to support moderate nocturnal CO₂ uptake rates by these succulent leaves.

     

Determinants of leaf temperature in California Mimulus species at different altitudes

Summary Leaf energy balance and gas-exchange characteristics were studied in Mimulus cardinalis at 400 m and Mimulus lewisii at 2,700 m in the Sierra Nevada of central California. In contrast to previous observations, leaf temperatures were not near 30° C at air temperatures from 20 to 40° C but were coupled quite closely to air temperature. Stomatal conductance in both species decreased in response to increases in the water vapor concentration gradient, a response opposite that required to establish 30°C leaf temperatures over a wide range of air temperatures. The temperature optima for photosynthesis were broad in both species but 5° C higher for M. cardinalis than for M. lewisii. The direct or indirect effects of altitude did not contribute significantly to the maintenance of constant leaf temperatures. For both species, maintaining constant leaf temperatures appears to be less important than avoiding inhibitory water stress or diffusion limitation of photosynthesis.     

Diffusive resistances at, and transpiration rates from leaves in situ within the vegetative canopy of a corn crop

At several heights and times of day within a crop of Zea mays, internal leaf diffusion resistance (r_i) and external boundary layer diffusion resistance (r_a) were evaluated by measuring the temperature of a transpiring and a non-transpiring leaf (simulated by covering both sides of a normal leaf with strips of poly-ethylene tape), and by measuring the immediate air temperature, humidity and windspeed.

Both r_a and r_i increased with depth into the crop. However, r_a generally was less than 10% of r_i.

Profiles of latent-heat flux density and source intensity of transpiration showed that transpiration corresponded roughly to foliage distribution (with an upward shift) and were not similar to the profile of radiation absorption.

The data were compared with heat budget data. The 2 approaches yielded quite similar height distributions of transpiration per unit leaf area and total transpiration resistance.

The total crop resistance to transpiration was computed as 0.027 min cm⁻¹. This compares to Monteith's values of 0.017 to 0.040 min cm⁻¹ for beans (Phaseolus vulgaris L.), and Linacre's values of 0.015 to 0.020 min cm⁻¹ for turf.

     

Light acclimation during and after leaf expansion in soybean

Soybean plants (Glycine max var. Ransom) were grown at light intensities of 850 and 250 μeinsteins m⁻² sec⁻¹ of photosynthetically active radiation. A group of plants was shifted from each environment into the other environment 24 hours before the beginning of the experiment. Net photosynthetic rates and stomatal conductances were measured at 2,000 and 100 μeinsteins m⁻² sec⁻¹ photosynthetically active radiation on the 1st, 2nd, and 5th days of the experiment to determine the time course of photosynthetic light adaptation. The following factors were also measured: dark respiration, leaf water potential, leaf thickness, internal surface area per external surface area, chlorophyll content, photosynthetic unit size and number, specific leaf weight, and activities of malate dehydrogenase, and glycolate oxidase. Comparisons were made with plants maintained in either 850 or 250 μeinsteins m⁻² sec⁻¹ environments. Changes in photosynthesis, stomatal conductance, leaf anatomy, leaf water potential, photosynthetic unit size, and glycolate oxidase activity occurred upon altering the light environment, and were complete within 1 day, whereas chlorophyll content, numbers of photosynthetic units, specific leaf weight, and malate dehydrogenase activity showed slower changes. Differences in photosynthetic rates at high light were largely accounted for by internal surface area differences with low environmental light associated with low internal area and low photosynthetic rate. An exception to this was the fact that plants grown at 250 μeinsteins m⁻² sec⁻¹ then switched to 850 μeinsteins m⁻² sec⁻¹ showed lower photosynthesis at high light than any other treatment. This was associated with higher glycolate oxidase and malate dehydrogenase activity. Photosynthesis at low light was higher in plants kept at or switched to the lower light environment. This increased rate was associated with larger photosynthetic unit size, and lower dark respiration and malate dehydrogenase activity. Both anatomical and physiological changes with environmental light occurred even after leaf expansion was complete and both were important in determining photosynthetic response to light.     

Temperature-dependent water and ion transport properties of barley and sorghum roots : I. Relationship to leaf growth

Root temperature strongly affects shoot growth, possibly via “nonhydraulic messengers” from root to shoot. In short-term studies with barley (Hordeum vulgare L.) and sorghum (Sorghum bicolor L.) seedlings, the optimum root temperatures for leaf expansion were 25° and 35°C, respectively. Hydraulic conductance (L_p) of both intact plants and detached exuding roots of barley increased with increasing root temperature to a high value at 25°C, remaining high with further warming. In sorghum, the L_p of intact plants and of detached roots peaked at 35°C. In both species, root temperature did not affect water potentials of the expanded leaf blade or the growing region despite marked changes in L_p. Extreme temperatures greatly decreased ion flux, particularly K⁺ and NO₃⁻, to the xylem of detached roots of both species. Removing external K⁺ did not alter short-term K⁺ flux to the xylem in sorghum but strongly inhibited flux at high temperature in barley, indicating differences in the sites of temperature effects. Leaf growth responses to root temperature, although apparently “uncoupled” from water transport properties, were correlated with ion fluxes. Studies of putative root messengers must take into account the possible role of ions.