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  • 1
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Abstract. A dynamic model of whole leaf C3 photosynthesis is constructed using a modified version of the Farquliar-von Caemmerer approach. The model is designed to provide a physiological basis to understand observations of assimilation in environments with varying photon flux densities, including induction phenomena. The model couples the effect of light activation and dark deactivation of enzymes, stomatal conductance responses, and variations in the pools of carbon cycle intermediates. The dynamic components are viewed on three time scales, the slowest of which (min to h) involves changes in stomatal conductance and the activation stale of Rubisco. On a time scale of seconds to a few minutes, adjustments in pools of biochemical components of the photosynthetic pathway occurs. The most rapid time scale corresponds to the equilibration time of intercelluar CO2 concentration through gaseous diffusion and is here assumed to occur instantaneously. The model form includes a single pool for reduced intermediates including RuBP, a single pool for components of the glycolate pathway, and a third component corresponding to the activation state of Rubisco. This is coupled to a previously described model for the dynamics of stomatal conductance, giving a final model form consisting of six non-linear ordinary differential equations, of which three control conductance dynamics and three control assimilation. The coupling between these occurs through the variable pi, the intercellular partial pressure of CO2. Only three of the parameters for the assimilation portion of the model require dynamic data to estimate. The remaining parameters are estimated from steady-state data. The model is calibrated using previously collected data on the tropical understory plant Alocasia macrorrhiza and is shown to have qualitatively similar behaviour to that of experimental measurements using simple changes in PFD, as well as a complex sequence of such changes.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Plant, cell & environment 17 (1994), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: The atmospheric CO2 concentration has increased from the pre-industrial concentration of about 280 μmol mol−1 to its present concentration of over 350 μmol mol−1, and continues to increase. As the rate of photosynthesis in C3 plants is strongly dependent on CO2 concentration, this should have a marked effect on photosynthesis, and hence on plant growth and productivity. The magnitude of photo-synthetic responses can be calculated based on the well-developed theory of photosynthetic response to intercellular CO2 concentration. A simple biochemically based model of photosynthesis was coupled to a model of stomatal conductance to calculate photosynthetic responses to ambient CO2 concentration. In the combined model, photosynthesis was much more responsive to CO2 at high than at low temperatures. At 350 μmol mol−1, photosynthesis at 35°C reached 51% of the rate that would have been possible with non-limiting CO2, whereas at 5°C, 77% of the CO2 non-limited rate was attained. Relative CO2 sensitivity also became smaller at elevated CO2, as CO2 concentration increased towards saturation. As photosynthesis was far from being saturated at the current ambient CO2 concentration, considerable further gains in photosynthesis were predicted through continuing increases in CO2 concentration. The strong interaction with temperature also leads to photosynthesis in different global regions experiencing very different sensitivities to increasing CO2 concentrations.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Plant, cell & environment 11 (1988), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Abstract. Seedlings of Eucalyptus pauciflora Sieb. ex. Spreng. were stressed by withholding water. They were then rewatered, and the time course of recovery of photosynthesis was followed. Recovery always followed a distinct bi-phasic pattern. A first, rapid, stage of recovery commenced between 5 and 60 min after rewatering and was completed by between 30 min and four h after rewatering. Recovery in this stage always involved concurrent increases in stomatal conductance and the leaf's capacity to assimilate CO2 at any intercellular partial pressure of CO2 [A(pi) relationship]. This stage of rapid recovery was followed either by a constant or gradually declining rate of photosynthesis for the remainder of the light period. In plants kept to a normal diurnal cycle, a second stage of recovery occurred and was completed during the night following rewatering. In this second stage of recovery, the A(Pi) relationship recovered to 90–100% of prestress values. In contrast, the recovery of stomatal conductance was not complete by the first day after rewatering. In darkness, complete recovery of the A(pi) relationship required as little as five h. If plants were kept in continuous high light, then between six and 16 h elapsed after rewatering before the second stage of recovery commenced. After this lag, almost complete recovery of the A(pi) relationship was possible. These results indicate that water stress has two independent and parallel effects on the mesophyll capacity for photosynthesis. The first may be simply reversible when the plant is rewatered, while the second may involve damage to the photosynthetic machinery that requires protein synthesis for its reversal.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: The growth rates of woody plants depend on both the rate of photosynthetic carbon gain and the availability of essential nutrients. Instantaneous carbon gain is known to increase in response to increasing atmospheric CO2 concentration, but it is uncertain whether this will translate into increased growth in the longer term under nutrient-limited conditions. An analytical model to address this question was developed by Comins & McMurtrie (1993, Ecological Applications 3, 666–681). Their model was further tested and analysed. Manipulation of various assumptions in the model revealed its key assumptions and allowed a more confident prediction of expected growth responses to CO2 enrichment under nutrient-limited conditions.The analysis indicated that conclusions about the CO2 sensitivity of production were strongly influenced by assumptions about the relationship between foliar and heartwood nitrogen concentrations. With heartwood nitrogen concentration proportional to foliar nitrogen concentration, the model predicted a strong response of plant productivity to increasing CO2 concentration, whereas with heartwood nitrogen concentration set constant, the model predicted only a very slight growth response to changing CO2 concentration. On the other hand, predictions were only slightly affected by: (1) assumptions about the extent of nitrogen retranslocation out of senescing roots and foliage or wood during heartwood formation; (2) the effects of nitrogen status on specific leaf area or (3) leaf longevity; (4) carbon allocation between different plant parts; or (5) changes in the N:C ratio of organic matter sequestered in the passive pool of soil organic matter. Modification of the effect of foliar nitrogen concentration on the light utilization coefficient had only a small effect on the CO2 sensitivity for pines. However, this conclusion was strongly dependent on the chosen relationship between single-leaf photosynthesis and leaf nitrogen concentration. Overall, the analysis suggested that trees growing under nitrogen-limited conditions can respond to increasing atmospheric CO2 concentration with considerable increases in growth.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Plant, cell & environment 11 (1988), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Abstract. Dynamic responses of stomatal conductance to lightflecks (15 s to 5 min) were observed in the tropical understory plant Alocasia macrorrhiza. Brief observations were also made on step changes in light, flashing light and short low-light periods (darkflecks) after stomata had reached steady state conductances in high light. Stomata opened substantially even in response to very short lightflecks, with maximal opening being reached about 20 min after the end of the lightfleck. These responses are compared to those of a semi-mechanistic stomatal model consisting of three steps in series: a biochemical signal which responds directly to light, producing osmotic changes within the guard cells which, in turn, drive the movement of water into the guard cells. The rate of change of each component was assumed to be given by the difference between the current state of that component and the state of the previous component in the series divided by a characteristic time constant for each step. This model allowed excellent description of observed responses to lightflecks, including the fleck-length dependence of stomatal opening, the lag between the end of the lightfleck and the time of maximal stomatal conductance and the response to multiple flecks. However, agreement with predicted responses to flashing light and darkflecks was poor. Good agreement could be restored by using different time constants for the initial biochemical step, suggesting that the speed of the initial biochemical response is not constant but dependent on the current physiological state of the stomata. For leaves experiencing predominantly low light, punctuated by relatively short and infrequent periods of high light, this model allows good description of the dynamic changes in stomatal conductance.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: The temperature dependence of C3 photosynthesis is known to vary with growth environment and with species. In an attempt to quantify this variability, a commonly used biochemically based photosynthesis model was parameterized from 19 gas exchange studies on tree and crop species. The parameter values obtained described the shape and amplitude of the temperature responses of the maximum rate of Rubisco activity (Vcmax) and the potential rate of electron transport (Jmax). Original data sets were used for this review, as it is shown that derived values of Vcmax and its temperature response depend strongly on assumptions made in derivation. Values of Jmax and Vcmax at 25 °C varied considerably among species but were strongly correlated, with an average Jmax : Vcmax ratio of 1·67. Two species grown in cold climates, however, had lower ratios. In all studies, the Jmax : Vcmax ratio declined strongly with measurement temperature. The relative temperature responses of Jmax and Vcmax were relatively constant among tree species. Activation energies averaged 50 kJ mol−1 for Jmax and 65 kJ mol−1 for Vcmax, and for most species temperature optima averaged 33 °C for Jmax and 40 °C for Vcmax. However, the cold climate tree species had low temperature optima for both Jmax(19 °C) and Vcmax (29 °C), suggesting acclimation of both processes to growth temperature. Crop species had somewhat different temperature responses, with higher activation energies for both Jmax and Vcmax, implying narrower peaks in the temperature response for these species. The results thus suggest that both growth environment and plant type can influence the photosynthetic response to temperature. Based on these results, several suggestions are made to improve modelling of temperature responses.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1365-2486
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Geography
    Notes: It is well recognized that photosynthesis of C3 plants is highly responsive to CO2 concentration. However, in natural ecosystems, plants are subject to a range of feed-back effects that can interact with increased photosynthetic carbon gain in different ways so that it is not clear to what extent increased photosynthesis will translate into increased growth. To assess the probable growth response of nutrient-limited forests to increasing CO2 concentration, we use a previously developed modelling framework and apply it under conditions where the supply of nutrients is affected by a range of different factors.Our analysis indicates that forest growth is likely to be highly stimulated by increasing CO2 concentration in forests with high fertility, in forests with nitrogen fixing plants, in those subject to fire or where nitrogen in wood is effectively removed from the biologically active cycle either through physical removal of stems in harvesting or through continued stem growth over long time periods. Forest growth is likely to be stimulated by CO2 concentration in both phosphorus- and sulphur-limited forests provided nutrients in heartwood of trees are removed from the active nutrient cycle. Without this removal from the cycling system, however, sulphur-limited forests should show little response to increasing CO2. In phosphorus-limited forests without phosphorus removal, the response to increasing CO2 depends further on the equilibration state of the large pool of unavailable secondary phosphorus. Considered over periods of centuries during which the secondary pool has equilibrated, growth of phosphorus-limited forests is likely to be only weakly stimulated by increasing CO2 concentration. However, over shorter periods, increasing CO2 concentration should lead to a substantial increase in productivity.In general, it can be concluded that systems that are more open with respect to nutrient gains and losses are likely to be more responsive to increasing CO2 concentration than systems where the amount of available nutrients is less variable. In more open systems, operation at a lower internal nutrient concentration as a result of increasing atmospheric CO2 concentration can lead to reduced nutrient losses per unit carbon gain. Our analysis shows that the effect of increasing CO2 on forest growth can differ substantially between forests due to interactions with a range of factors that affect nutrient supply. The response of a particular forest to increasing CO2 concentration can only be predicted if the main factors controlling nutrient supply and growth in that forest are understood and incorporated into an assessment.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Oecologia 70 (1986), S. 273-282 
    ISSN: 1432-1939
    Keywords: Photosynthetic capacity ; Stomata ; Carboxylation efficiency ; Eucalyptus ; Acacia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The rate of CO2 assimilation at light saturation and an intercellular CO2 concentration of 350 μl l-1 (photosynthetic capacity), measured in leaves of Eucalyptus pauciflora, E. behriana, E. delegatensis and Acacia melanoxylon, declined over the course of cloudless days under naturally varying environmental conditions as well as under constant optimal conditions for high CO2 uptake. Since the capacity did not recover during the light period, it was different from the “midday depression” of gas exchange. The change appeared to be caused neither by the diurnal variation of total leaf water potential, by photoinhibition of redox-reaction centres in photosystems nor by changes in the intrinsic properties of Ribulose-bisphosphate carboxylase-oxygenase. The decline was more pronounced in winter than in summer. It was related to the duration of illumination or the cumulative carbon gain. It was reversible in the following dark phase, and it did not occur on changeable days with short peaks of high light. Despite the decline in photosynthetic capacity, the initial slope of the CO2 response of net photosynthesis, as obtained at low intercellular CO2 concentrations, remained constant during the day, but declined at night when photosynthetic capacity recovered. In all cases stomatal conductance varied in parallel with photosynthetic capacity. The relevance of changes in photosynthetic capacity for the intercellular CO2 concentration is discussed.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-2048
    Keywords: Key words:Alocasia (photosynthesis) ; Light activation (Rubisco) ; Lightfleck (carbon gain) ; Model (photo-synthesis) ; Photosynthesis ; Photosynthetic induction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract. Photosynthetic carbon gain in rapidly fluctuating light is controlled by stomatal conductance, activation of ribulose-1,5-bisphosphate carboxylase-oxygenase, a fast induction step in the regeneration of ribulose-1,5-bisphosphate, and the build-up of pools of photosynthetic intermediates that allow post-illumination CO2 fixation. Experimental work over recent years has identified and characterised these factors. A physiologically-based dynamic model is described here that incorporates these factors and allows the simulation of carbon gain in response to any arbitrary sequence of light levels. The model output is found to conform well to previously reported plant responses of Alocasia macrorrhiza (L.) G. Don. observed under widely differing conditions. The model shows (i) responses of net assimilation rate and stomatal conductance to constant light levels and different CO2 concentrations that are consistent with experimental observations and predictions of a steady-state model; (ii) carbon gain to continue after the end of lightflecks, especially in uninduced leaves; (iii) carbon gain to be only marginally reduced during low-light periods of up to 2 s; (iv) a fast-inducing component in the regeneration of ribulose-1,5-bisphosphate to be limiting for up to 60 s after an increase in light in uninduced leaves: the duration of this limitation lengthens with increasing CO2 concentration and is absent at low CO2 concentration; (v) oxygen evolution to exceed CO2 fixation during the first few seconds of a lightfleck, but CO2 fixation to continue after the end of the lightfleck whereas oxygen evolution decreases to low-light rates immediately. The model is thus able to reproduce published responses of leaves to a variety of perturbations. This provides good evidence that the present formulation of the model includes the essential rate-determining factors of photosynthesis under fluctuating light conditions.
    Type of Medium: Electronic Resource
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