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  • Canopy conductance  (2)
  • Heterosis  (2)
  • Nicotiana (transformed with antisense DNA)  (2)
  • Springer  (6)
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  • Springer  (6)
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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Oecologia 95 (1993), S. 153-163 
    ISSN: 1432-1939
    Keywords: Evaporation ; Aerodynamic conductance ; Canopy conductance ; Humidity response ; Soil water
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Canopy-scale evaporation rate (E) and derived surface and aerodynamic conductances for the transfer of water vapour (gs and ga, respectively) are reviewed for coniferous forests and grasslands. Despite the extremes of canopy structure, the two vegetation types have similar maximum hourly evaporation rates (E max) and maximum surface conductances (gsmax) (medians = 0.46 mm h-1 and 22 mm s-1). However, on a daily basis, median E max of coniferous forest (4.0 mm d-1) is significantly lower than that of grassland (4.6 mm d-1). Additionally, a representative value of ga for coniferous forest (200 mm s-1) is an order of magnitude more than the corresponding value for grassland (25 mm s-1). The proportional sensitivity of E, calculated by the Penman-Monteith equation, to changes in gs is 〉0.7 for coniferous forest, but as low as 0.3 for grassland. The proportional sensitivity of E to changes in ga is generally ±0.15 or less. Boundary-line relationships between gs and light and air saturation deficit (D) vary considerably. Attainment of gsmax occurs at a much lower irradiance for coniferous forest than for grassland (15 versus about 45% of full sunlight). Relationships between gs and D measured above the canopy appear to be fairly uniform for coniferous forest, but are variable for grassland. More uniform relationships may be found for surfaces with relatively small ga, like grassland, by using D at the evaporating surface (D0) as the independent variable rather than D at a reference point above the surface. An analytical expression is given for determining D0 from measurable quantities. Evaporation rate also depends on the availability of water in the root zone. Below a critical value of soil water storage, the ratio of evaporation rate to the available energy tends to decrease sharply and linearly with decreasing soil water content. At the lowest value of soil water content, this ratio declines by up to a factor of 4 from the non-soil-water-limiting plateau. Knowledge about functional rooting depth of different plant species remains rather limited. Ignorance of this important variable makes it generally difficult to obtain accurate estimates of seasonal evaporation from terrestrial ecosystems.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1939
    Keywords: Canopy conductance ; Canopy transpiration ; Xylem sap flow ; Humidity response of stomatal ; Nothofagus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    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.
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  • 3
    ISSN: 1432-2048
    Keywords: Flux control (photosynthesis) ; Nicotiana (transformed with antisense DNA) ; Ribulose-1,5-bisphosphate carboxylase-oxygenase (control of photosynthesis) ; Transgenic plant (antisense)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Transgenic tobacco (Nicotiana tabacum L.) plants transformed with ‘antisense’ rbcS to produce a series of plants with a progressive decrease in the amount of ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) have been used to investigate the contribution of Rubsico to the control of photosynthesis at different irradiance, CO2 concentrations and vapour-pressure deficits. Assimilation rates, transpiration, the internal CO2 concentration and chlorophyll fluorescence were measured in each plant. (i) The flux-control coefficient of Rubisco was estimated from the slope of the plot of Rubisco content versus assimilation rate. The flux-control coefficient had a value of 0.8 or more in high irradiance, (1050 μmol·m−2·s−1), low-vapour pressure deficit (4 mbar) and ambient CO2 (350 μbar). Control was marginal in enhanced CO2 (450 μbar) or low light (310 μmol·m−2·s−1) and was also decreased at high vapour-pressure deficit (17 mbar). No control was exerted in 5% CO2. (ii) The flux-control coefficients of Rubisco were compared with the fractional demand placed on the calculated available Rubisco capacity. Only a marginal control on photosynthetic flux is exerted by Rubisco until over 50% of the available capacity is being used. Control increases as utilisation rises to 80%, and approaches unity (i.e. strict limitation) when more than 80% of the available capacity is being used. (iii) In low light, plants with reduced Rubisco have very high energy-dependent quenching of chlorophyll fluorescence (qE) and a decreased apparent quantum yield. It is argued that Rubisco still exerts marginal control in these conditions because decreased Rubisco leads to increased thylakoid energisation and high-energy dependent dissipation of light energy, and lower light-harvesting efficiency. (iv) The flux-control coefficient of stomata for photosynthesis was calculated from the flux-control coefficient of Rubisco and the internal CO2 concentration, by applying the connectivity theorem. Control by the stomata varies between zero and about 0.25. It is increased by increased irradiance, decreased CO2 or decreased vapour-pressure deficit. (v) Photosynthetic oscillations in saturating irradiance and CO2 are suppressed in decreased-activity transformants before the steady-state rate of photosynthesis is affected. This provides direct evidence that these oscillations reveal the presence of “excess” Rubisco. (vi) Comparison of the flux-control coefficients of Rubisco with mechanistic models of photosynthesis provides direct support for the reliability of these models in conditions where Rubisco has a flux-control coefficient approach unity (i.e. “limits” photosynthesis), but also indicates that these models are less useful in conditions where control is shared between Rubisco and other components of the photosynthetic apparatus.
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  • 4
    ISSN: 1432-2048
    Keywords: Nicotiana (transformed with antisense DNA) ; Photosynthesis ; Ribulose-1,5-bisphosphate carboxylase-oxygenase ; Transgenic plant (antisense)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Experiments were carried out to determine how decreased expression of ribulose-1,5-bisphosphate carboxylase-oxygenase (Rubisco) affects photosynthetic metabolism in ambient growth conditions. In a series of tobacco (Nicotiana tabacum L.) plants containing progressively smaller amounts of Rubisco the rate of photosynthesis was measured under conditions similar to those in which the plants had been grown (310 μmol photons · m−2 · s−1, 350 μbar CO2, 22° C). (i) There was only a marginal inhibition (6%) of photosynthesis when Rubisco was decreased to about 60% of the amount in the wildtype. The reduced amount of Rubisco was compensated for by an increase in Rubisco activation (rising from 60 to 100%), with minor contributions from an increase of its substrates (ribulose-1,5-bisphosphate and the internal CO2 concentration) and a decrease of its product (glycerate-3-phosphate). (ii) The decreased amount of Rubisco was accompanied by an increased ATP/ADP ratio that may be causally linked to the increased activation of Rubisco. An increase of highenergy-state chlorophyll fluorescence shows that thylakoid membrane energisation and high-energy-state-dependent energy dissipation at photosystem two had also increased. (iii) A further decrease of Rubisco (in the range of 50–20% of the wildtype level) resulted in a strong and proportional inhibition of CO2 assimilation. This was accompanied by a decrease of fructose-1,6-bisphosphatase activity, coupling-factor 1 (CF1)-ATP-synthase protein, NADP-malate dehydrogenase protein, and chlorophyll. The chlorophyll a/b ratio did not change, and enolase and sucrose-phosphate synthase activity did not decrease. It is argued that other photosynthetic enzymes are also decreased once Rubisco decreases to the point at which it becomes strongly limiting for photosynthesis. (iv) It is proposed that the amount of Rubisco in the wildtype represents a balance between the demands of light, water and nitrogen utilisation. The wildtype overinvests about 15% more protein in Rubisco than is needed to avoid a strict Rubisco limitation of photosynthesis. However, this “excess” Rubisco allows the wildtype to operate with lower thylakoid energisation, and decreased high-energy-state-dependent energy dissipation, hence increasing light-use efficiency by about 6%. It also allows the wildtype to operate with a lower internal CO2 concentration in the leaf and a lower stomatal conductance at a given rate of photosynthesis, so that instantaneous water-use efficiency is marginally (8%) increased.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Trees 1 (1987), S. 219-224 
    ISSN: 1432-2285
    Keywords: Larix ; Heterosis ; Photosynthesis ; Stomatal conductance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Individual 33-year-old forest trees of the deciduous conifer speciesLarix decidua, Larix leptolepis andLarix decidua x leptolepis were investigated with respect to the phenomenon of stem heterosis in hybrid larch; the first part of this study compares the gas exchange responses of leaves. CO2 assimilation per leaf area was similar in the three larch species, but on a dry weight basis the nitrogen content of the needles and maximum CO2 assimilation rate (Amax) were slightly higher in the hybrid. This increase was accompanied by a higher protein content than in the Japanese and a lower specific leaf weight than in the European larch. All three species were similar in terms of the photosynthetic “nitrogen use” and stomatal conductance atA max. The similar slopes of the area-related steady-state responses of gas exchange against irradiance, evaporative demand and internal CO2 concentration led to similar rates of CO2 uptake under ambient conditions. The natural combinations and variability of the environmental factors also reduced the small dry weight-related difference inA max between hybrid larch and the parent species, such that all trees achieved similar daily carbon gains. Thus, the ecological significance of small interspecific differences in the metabolism of leaves has very little effect under the natural habitat conditions of a temperate climate. The second part of the study will investigate the effect of growth characteristics on the heterosis of hybrid larch.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Trees 1 (1987), S. 225-231 
    ISSN: 1432-2285
    Keywords: Larix ; Heterosis ; Growth ; Branching pattern ; Needle density
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Among 33-year-old forest trees ofLarix decidua, L. leptolepis andL. decidua x leptolepis, the hybrid possessed an above-ground biomass which was three times greater, although all larches displayed similar relative distributions of biomass. At a “relative growth rate” slightly lower than in the parent species, hybrid larch achieved twice the annual carbon gain, increment in stem length and above-ground production, and its foliage-related stem growth was higher than in European (L. decidua) but similar to Japanese (L. leptolepis) larch. A similar “relative growth efficiency” and foliage-related total above-ground production in all trees did reflect the similarity of photosynthetic capacity of the hybrid found at the leaf level. While the lengths of lateral twigs on hybrid branches were intermediate between the European larch with short, and the Japanese larch with large, twigs the hybrid possessed the longest branches with the highest needle biomass. This resulted in a crown structure of the hybrid crown similar to the Japanese larch together with a high needle density on branches as in the European larch. In total, the foliage biomass per crown length was about 30% higher in hybrid larch than in both of the parent species. Thus, the high carbon input for the stem heterosis was based on a “complementation principle” of advantageous parent features at the crown level. Similar slopes of foliage against sapwood area of stem and branches did not indicate a special need for a thick hybrid stem with respect to water transport.
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