ALBERT

Notes: Sunflower plants [Helianthus annuus L.) were subjected to soil drought. Leaf conductance declined with soil water content even when the shoot was kept turgid throughout the drying period. The concentration of abscisic acid in the xylem sap increased with decreasing soil water content. No general relation could be established between abscisic acid concentration in the xylem sap and leaf conductance due to marked differences in the sensitivity of leaf conductance of individual plants to abscisic acid from the xylem sap. The combination of these results with data from Gollan, Schurr & Schulze (1992, see pp. 551–559, this issue) reveals close connection of the effectiveness of abscisic acid as a root to shoot signal to the nutritional status of the plant.

Notes: Higher rates of nitrate assimilation are required to support faster growth in enhanced carbon dioxide. To investigate how this is achieved, tobacco plants were grown on high nitrate and high light in ambient and enhanced (700 μmol mol–1) carbon dioxide. Surprisingly, enhanced carbon dioxide did not increase leaf nitrate reductase (NR) activity in the middle of the photoperiod. Possible reasons for this anomalous result were investigated. (a) Measurements of biomass, nitrate, amino acids and glutamine in plants fertilized once and twice daily with 12 mol m–3 nitrate showed that enhanced carbon dioxide did not lead to a nitrate limitation in these plants. (b) Enhanced carbon dioxide modified the diurnal regulation of NR activity in source leaves. The transcript for nia declined during the light period in a similar manner in ambient and enhanced carbon dioxide. The decline of the transcript correlated with a decrease of nitrate in the leaf, and was temporarily reversed after re-irrigating with nitrate in the second part of the photoperiod. The decline of the transcript was not correlated with changes of sugars or glutamine. NR activity and protein decline in the second part of the photoperiod, and NR is inactivated in the dark in ambient carbon dioxide. The decline of NR activity was smaller and dark inactivation was partially reversed in enhanced carbon dioxide, indicating that post-transcriptional or post-translational regulation of NR has been modified. The increased activation and stability of NR in enhanced carbon dioxide was correlated with higher sugars and lower glutamine in the leaves. (c) Enhanced carbon dioxide led to increased levels of the minor amino acids in leaves. (d) Enhanced carbon dioxide led to a large decrease of glycine and a small decrease of serine in leaves of mature plants. The glycine:serine ratio decreased in source leaves of older plants and seedlings. The consequences of a lower rate of photorespiration for the levels of glutamine and the regulation of nitrogen metabolism are discussed. (e) Enhanced carbon dioxide also modified the diurnal regulation of NR in roots. The nia transcript increased after nitrate fertilization in the early and the second part of the photoperiod. The response of the transcript was not accentuated in enhanced carbon dioxide. NR activity declined slightly during the photoperiod in ambient carbon dioxide, whereas it increased 2-fold in enhanced carbon dioxide. The increase of root NR activity in enhanced carbon dioxide was preceded by a transient increase of sugars, and was followed by a decline of sugars, a faster decrease of nitrate than in ambient carbon dioxide, and an increase of nitrite in the roots. (f) To interpret the physiological significance of these changes in nitrate metabolism, they were compared with the current growth rate of the plants. (g) In 4–5-week-old plants, the current rate of growth was similar in ambient and enhanced carbon dioxide (≈ 0·4 g–1 d–1). Enhanced carbon dioxide only led to small changes of NR activity, nitrate decreased, and overall amino acids were not significantly increased. (h) Young seedlings had a high growth rate (0·5 g–1 d–1) in ambient carbon dioxide, that was increased by another 20% in enhanced carbon dioxide. Enhanced carbon dioxide led to larger increases of NR activity and NR activation, a 2–3-fold increase of glutamine, a 50% increase of glutamate, and a 2–3-fold increase in minor amino acids. It also led to a higher nitrate level. It is argued that enhanced carbon dioxide leads to a very effective stimulation of nitrate uptake, nitrate assimilation and amino acid synthesis in seedlings. This will play an important role in allowing faster growth rates in enhanced carbon dioxide at this stage.

Notes: Sunflower plants (Helianthus annuus L.) were subjected to soil drying with their shoots either kept fully turgid using a Passioura-type pressure chamber or allowed to decrease in water potential. Whether the shoots were kept turgid or not, leaf conductance decreased below a certain soil water content. During the soil drying, xylem sap samples were taken from individual intact and transpiring plants. Xylem sap concentrations of nitrate and phosphate decreased with soil water content, whereas the concentrations of the other anions (SO42 and Cl−) remained unaltered. Calcium concentrations also decreased. Potassium, magnesium, manganese and sodium concentrations stayed constant during soil drying. In contrast, the pH, the buffering capacity at a pH below 5 and the cation/anion ratio increased after soil water content was lowered below a certain threshold. Amino acid concentration of the xylem sap increased with decreasing soil water content. The effect of changes in ion concentrations in the xylem sap on leaf conductance is discussed.

Notes: Abstract Downward transport of water in roots, in the following termed “inverse hydraulic lift,” has previously been shown with heat flux techniques. But water flow into deeper soil layers was demonstrated in this study for the first time when investigating several perennial grass species of the Kalahari Desert under field conditions. Deuterium labelling was used to show that water acquired by roots from moist sand in the upper profile was transported through the root system to roots deeper in the profile and released into the dry sand at these depths. Inverse hydraulic lift may serve as an important mechanism to facilitate root growth through the dry soil layers underlaying the upper profile where precipitation penetrates. This may allow roots to reach deep sources of moisture in water-limited ecosystems such as the Kalahari Desert.

Notes: Summary Previous publications have reported on investigations of CO2 exchange in the desert lichenRamalina maciformis both in its natural habitat in the Negev and in the laboratory. Utilizing laboratory data, net photosynthesis and dark respiration were expressed as mathematical functions of the most important environmental factors. Based on these relationships, a model is developed that allows one to predict CO2 exchange of the plant. Input data are light intensity, temperature, and water content of the thallus, together with a measure of the rate of the seasonal change of photosynthetic and respiratory activity. The validity of the model is tested by comparing simulated daily courses of CO2 uptake and release of the lichen with independent results of CO2 exchange measurements conducted in the field during and after the condensation of dew. The sensitivity of the model is shown by simulating changes in the input data of temperature and water content of the lichen.

Notes: Summary Biomass distribution and diurnal CO2 uptake under natural conditions were investigated on Picea abies in a mountainous climate (Solling, Northwest Germany). Spruce has a remarkable variability in leaf characteristics. Even on a single branch in the lower sun crown, needle dry weight and surface area change considerably from the branch base to the tip and accoring to exposure. Only about 18% of the total biomass of the tree was current year's growth, about 40% of the needles were 4 years and older reaching a maximal age of 12 years. The main growing zone was at the border of upper shade and lower sun crown and the main accumulation of dry weight was at a greater tree height than was observed for maximal growth of needle numbers or surface area. The annual, new growth shifted toward the upper sun crown. Maximal daily CO2 uptake was highest in the lower sun crown on days with variable cloud cover when temperatures were moderate and water vapor pressure deficits were low. Also the annual CO2 uptake was highest in the lower sun crown, where 4-year-old and older needles contributed about 35% to the annual CO2 uptake of the tree. Current year growth contributed about 15% of the total CO2 gain. The upper and lower sun crowns produce about 70% of the total carbon gain. The carbon balance of spruce and the distribution of the production process in relation to needle age and crown level are discussed.

Notes: Summary Net photosynthesis of Picea abies was measured in a spruce forest in northern Germany with temperature- and humidity-controlled cuvettes in 4 different crown layers on shoots of different ages. These measurments were performed such that temperature and humidity either followed ambient conditions or were kept constant. Annual courses of light-, temperature-, and humidity-related net photosynthesis were determined. Spruce had a remarkably constant rate of CO2 uptake from April to September for 1-year and older needles. Light saturation was achieved at 25 klx. Current year needles had the highest rates of CO2 uptake in early summer, but these rates decreased by autumn. Photosynthetic capacity decreased with needle age and, on a dry weight basis, it was higher in the shade than in the sun crown. The temperature optimum was between 13 and 23° C. Photosynthesis in spruce decreased when air humidity was low. The effect of the natural weather conditions on photosynthetic capacity was determined. The habitat is characterized by a high frequency of low light intensities (75% of total daytime below 20 klx) and cool temperatures (80% of daytime between 9 and 21° C). Low air humidity was only present when light intensities were high. The major limiting factor for production was low light intensities, which reduced photosynthetic capacity in the sun crown to 42% below maximum possible rates. Adverse temperatures reduced CO2 uptake by 28% and large water vapor pressure deficits reduced rates by only 2% compared with maximum possible rates. The limited adaptation to light is discussed.

Notes: Summary Growth and CO2 uptake in the crown of a spruce tree is described and the production processes of this evergreen conifer are compared with those of a deciduous beech. Spruce had 60% lower rates of net photosynthesis per dry weight than beech. But, beech had a 30% shorter growing season and a 84% smaller biomass than spruce. The annual CO2 gain was 40% lower in beech than it was in spruce. An analysis shows the following conclusions for this habitat. (1) The effect of a prolonged growing season is small. The annual CO2 gain of spruce would be reduced only by 9% if the growing season was the same length as for beech. (2) The annual CO2 gain would increase 14% if all needles in spruce were deciduous, because the current year needles have a higher average rate of CO2 uptake than 3-year old and older needles, but a lower average rate than 1- and 2-year old ones. However, the carbon balance of the tree shows that spruce could not afford to produce the existing needle biomass (14 t ha-1) each year. (3) If spruce were to produce the same deciduous foliage biomass during the same growing season as beech then total production by spruce would be reduced 67%. (4) The annual CO2 uptake by evergreen spruce was higher than deciduous beech not because of a long growing season, but because of the longevity of its needles, which during their total life time (an average of 5 years) have a two to three times greater CO2 uptake than a deciduous leaf in one summer season. The relatively small investment in current year needles produces an annually low, but long lasting assimilation of CO2.

Notes: Abstract The effect of nitrogen supply during growth on the contribution of ribulose-1,5-bisphosphate carboxylase-oxygenase (Rubisco; EC 4.1.1.39) to the control of photosynthesis was examined in tobacco (Nicotiana tabacum L.). Transgenic plants transformed with antisense rbcS to produce a series of plants with a progressive decrease in the amount of Rubisco were used to allow the calculation of the flux-control coefficient of Rubisco for photosynthesis (CR). Several points emerged from the data: (i) The strength of Rubisco control of photosynthesis, as measured by CR, was altered by changes in the short-term environmental conditions. Generally, CR was increased in conditions of increased irradiance or decreased CO2. (ii) The amount of Rubisco in wild-type plants was reduced as the nitrogen supply during growth was reduced and this was associated with an increase in CR. This implied that there was a specific reduction in the amount of Rubisco compared with other components of the photosynthetic machinery. (iii) Plants grown with low nitrogen and which had genetically reduced levels of Rubisco had a higher chlorophyll content and a lower chlorophyll a/b ratio than wild-type plants. This indicated that the nitrogen made available by genetically reducing the amount of Rubisco had been re-allocated to other cellular components including light-harvesting and electron-transport proteins. It is argued that there is a “luxury” additional investment of nitrogen into Rubisco in tobacco plants grown in high nitrogen, and that Rubisco can also be considered a nitrogen-store, all be it one where the opportunity cost of the nitrogen storage is higher than in a non-functional storage protein (i.e. it allows for a slightly higher water-use efficiency and for photosynthesis to respond to temporarily high irradiance).

Notes: 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.