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  • 1
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Ecology, Evolution, and Systematics 23 (1992), S. 201-235 
    ISSN: 0066-4162
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Global change biology 5 (1999), S. 0 
    ISSN: 1365-2486
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Geography
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Global change biology 5 (1999), S. 0 
    ISSN: 1365-2486
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Geography
    Notes: The distribution of assimilated carbon among the plant parts has a profound effect on plant growth, and at a larger scale, on terrestrial biogeochemistry. Although important progress has been made in modelling photosynthesis, less effort has been spent on understanding the carbon allocation, especially at large spatial scales. Whereas several individual-level models of plant growth include an allocation scheme, most global terrestrial models still assume constant allocation of net primary production (NPP) among plant parts, without any environmental coupling. Here, we use the CASA biosphere model as a platform for exploring a new global allocation scheme that estimates allocation of photosynthesis products among leaves, stems, and roots depending on resource availability. The philosophy underlying the model is that allocation patterns result from evolved responses that adjust carbon investments to facilitate capture of the most limiting resources, i.e. light, water, and mineral nitrogen. In addition, we allow allocation of NPP to vary in response to changes in atmospheric CO2. The relative magnitudes of changes in NPP and resource-use efficiency control the response of root:shoot allocation. For ambient CO2, the model produces realistic changes in above-ground allocation along productivity gradients. In comparison to the CASA standard estimate using fixed allocation ratios, the new allocation scheme tends to favour root allocation, leading to a 10% lower global biomass. Elevated CO2, which alters the balance between growth and available resources, generally leads to reduced water stress and consequently, decreased root:shoot ratio. The major exception is forest ecosystems, where increased nitrogen stress induces a larger root allocation.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1365-2486
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Geography
    Notes: Soil and ecosystem trace gas fluxes are commonly measured using the dynamic chamber technique. Although the chamber pressure anomalies associated with this method are known to be a source of error, their effects have not been fully characterized. In this study, we use results from soil gas-exchange experiments and a soil CO2 transport model to characterize the effects of chamber pressure on soil CO2 efflux in an annual California grassland. For greater than ambient chamber pressures, experimental data show that soil-surface CO2 flux decreases as a nonlinear function of increasing chamber pressure; this decrease is larger for drier soils. In dry soil, a gauge pressure of 0.5 Pa reduced the measured soil CO2 efflux by roughly 70% relative to the control measurement at ambient pressure. Results from the soil CO2 transport model show that pressurizing the flux chamber above ambient pressure effectively flushes CO2 from the soil by generating a downward flow of air through the soil air-filled pore space. This advective flow of air reduces the CO2 concentration gradient across the soil–atmosphere interface, resulting in a smaller diffusive flux into the chamber head space. Simulations also show that the reduction in diffusive flux is a function of chamber pressure, soil moisture, soil texture, the depth distribution of soil CO2 generation, and chamber diameter. These results highlight the need for caution in the interpretation of dynamic chamber trace gas flux measurements. A portion of the frequently observed increase in net ecosystem carbon uptake under elevated CO2 may be an artifact resulting from the impact of chamber pressurization on soil CO2 efflux.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1365-2486
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Geography
    Notes: Remote sensing of net primary production (NPP) is a critical tool for assessing spatial and temporal patterns of carbon exchange between the atmosphere and biosphere. However, satellite estimates suffer from a lack of large-scale field data needed for validation, as well as the need to parameterize plant light-use efficiencies (LUEs). In this study, we estimated cropland NPP with the Carnegie-Ames-Stanford-Approach (CASA), a biogeochemical model driven by satellite observations, and then compared these results with field estimates based on harvest data from United States Department of Agriculture National Agriculture Statistics Service (NASS) county statistics. Observed interannual variations in NPP over a 17-year period were well modelled by CASA, with exceptions mainly due to occasional difficulties in estimating NPP from harvest yields. The role of environmental stressors in agriculture was investigated by running CASA with and without temperature and moisture down-regulators, which are used in the model to simulate climate impacts on plant LUE. In most cases, correlations with NASS data were highest with modelled stresses, while the opposite was true for irrigated and temperature resistant crops. Analysis of the spatial variability in computed LUE revealed significantly higher values for corn than for other crops, suggesting a simple parameterization of LUE for future studies based on the fraction of area with corn. Absolute values of LUE were much lower than those reported in field trials, due to uncommonly high yields in most field trials, as well as overestimates of absorbed radiation in CASA attributed to bias from temporal compositing of satellite data. Total NPP for US croplands, excluding Alaska and Hawaii, was estimated as 0.62 Pg C year−1, representing ∼20% of total US NPP, and exhibited a positive trend of 3.7 Tg C year−2. These results have several implications for large-scale carbon cycle research that are discussed, and are especially relevant for studies of the role of agriculture in the global carbon balance.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Plant, cell & environment 20 (1997), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Disease is an integral element of agricultural and natural systems, but the roles pathogens play in determining ecosystem response to elevated CO2 have rarely been examined. To investigate whether disease can alter the response of plants to CO2, we examined the effects of doubled CO2 (∼700 μmol mol−1) on Avena sativa infected with barley yellow dwarf virus (BYDV), a common pathogen of cereals and grasses. Oats infected with BYDV showed a significantly greater biomass response to CO2 enrichment than did healthy plants. Root mass of diseased plants increased by 37–60% with CO2 enrichment, but was largely unaffected in healthy plants. CO2 enrichment increased midday leaf-level photosynthesis and instantaneous water use efficiency by 34 and 93% in healthy plants and by 48 and 174% in infected plants. Foliar carbohydrates increased with both CO2 enrichment and BYDV infection, but the two factors affected individual pools dissimilarly. CO2 enrichment may alter the epidemiology of BYDV by increasing the persistence of infected plants.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Plant, cell & environment 18 (1995), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Increased atmospheric CO2 often but not always leads to large decreases in leaf conductance. Decreased leaf conductance has important implications for a number of components of CO2 responses, from the plant to the global scale. All of the factors that are sensitive to a change in soil moisture, either amount or timing, may be affected by increased CO2. The list of potentially sensitive processes includes soil evaporation, run-off, decomposition, and physiological adjustments of plants, as well as factors such as canopy development and the composition of the plant and microbial communities. Experimental evidence concerning ecosystem-scale consequences of the effects of CO2 on water use is only beginning to accumulate, but the initial indication is that, in water-limited areas, the effects of CO2-induced changes in leaf conductance are comparable in importance to those of CO,2-induced changes in photosynthesis.Above the leaf scale, a number of processes interact to modulate the response of canopy or regional evapotran-spiration to increased CO2. While some components of these processes tend to amplify the sensitivity of evapo-transpiration to altered leaf conductance, the most likely overall pattern is one in which the responses of canopy and regional evapotranspiration are substantially smaller than the responses of canopy conductance. The effects of increased CO2 on canopy evapotranspiration are likely to be smallest in aerodynamically smooth canopies with high leaf conductances. Under these circumstances, which are largely restricted to agriculture, decreases in evapotranspiration may be only one-fourth as large as decreases in canopy conductance.Decreased canopy conductances over large regions may lead to altered climate, including increased temperature and decreased precipitation. The simulation experiments to date predict small effects globally, but these could be important regionally, especially in combination with radiative (greenhouse) effects of increased CO2.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Previous modelling exercises and conceptual arguments have predicted that a reduction in biochemical capacity for photosynthesis (Aarea) at elevated CO2 may be compensated by an increase in mesophyll tissue growth if the total amount of photosynthetic machinery per unit leaf area is maintained (i.e. morphological upregulation). The model prediction was based on modelling photosynthesis as a function of leaf N per unit leaf area (Narea), where Narea = Nmass×LMA. Here, Nmass is percentage leaf N and is used to estimate biochemical capacity and LMA is leaf mass per unit leaf area and is an index of leaf morphology. To assess the relative importance of changes in biochemical capacity versus leaf morphology we need to control for multiple correlations that are known, or that are likely to exist between CO2 concentration, Narea, Nmass, LMA and Aarea. Although this is impractical experimentally, we can control for these correlations statistically using systems of linear multiple-regression equations. We developed a linear model to partition the response of Aarea to elevated CO2 into components representing the independent and interactive effects of changes in indexes of biochemical capacity, leaf morphology and CO2 limitation of photosynthesis. The model was fitted to data from three pine and seven deciduous tree species grown in separate chamber-based field experiments. Photosynthetic enhancement at elevated CO2 due to morphological upregulation was negligible for most species. The response of Aarea in these species was dominated by the reduction in CO2 limitation occurring at higher CO2 concentration. However, some species displayed a significant reduction in potential photosynthesis at elevated CO2 due to an increase in LMA that was independent of any changes in Narea. This morphologically based inhibition of Aarea combined additively with a reduction in biochemical capacity to significantly offset the direct enhancement of Aarea caused by reduced CO2 limitation in two species. This offset was 100% for Acer rubrum, resulting in no net effect of elevated CO2 on Aarea for this species, and 44% for Betula pendula. This analysis shows that interactions between biochemical and morphological responses to elevated CO2 can have important effects on photosynthesis.
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  • 9
    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: At elevated atmospheric CO2 concentrations ([CO2]a), photosynthetic capacity (Amax) and root fraction (ηR, the ratio of root to plant dry mass) increased in some studies and decreased in others. Here, we have explored possible causes of this, focusing on the relative magnitudes of the effects of elevated [CO2]a on specific leaf (nm) and plant (np) nitrogen concentrations, leaf mass per unit area (h), and plant nitrogen productivity (α). In our survey of 39 studies with 35 species, we found that elevated [CO2]a led to decreased nm and np in all the studies and to increased h and α in most of the studies. The magnitudes of these changes varied with species and with experimental conditions.Based on a model that integrated [CO2]a-induced changes in leaf nitrogen into a biochemically based model of leaf photosynthesis, we predicted that, to a first approximation, photosynthesis will be upregulated (Amax will increase) when growth at increased [CO2]a leads to increases in h that are larger than decreases in nm. Photosynthesis will be downregulated (Amax will decrease) when increases in h are smaller than decreases in nm. The model suggests that photosynthetic capacity increases at elevated [CO2]a only when additional leaf mesophyll more than compensates the effects of nitrogen dilution.We considered two kinds of regulatory paradigms that could lead to varying responses of ηR to elevated [CO2]a, and compared the predictions of each with the data. A simple static model based on the functional balance concept predicts that ηR should increase when neither np nor h is very responsive to elevated [CO2]a. The quantitative and qualitative agreement of the predictions with data from the literature, however, is poor. A model that predicts ηR from the relative sensitivities of photosynthesis and relative growth rate to elevated [CO2]a corresponds much more closely to the observations. In general, root fraction increases if the response of photosynthesis to [CO2]a is greater than that of relative growth rate.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Plant, cell & environment 14 (1991), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Abstract. Sunflower plants (Helianthus annuus L., cv. CGL 208) were field-grown in adjacent plots of varying resource availability. Control plants received irrigation (on a 4–5 d interval) and high levels of fertilizer nitrogen. Nutrient-stress (N-stress) plants received control levels of irrigation but no nutrient amendments and were determined to be nitrogen-limited. Water-stress (H2O-stress) plants received control levels of fertilizer nitrogen, but no irrigation after approximately 6 weeks of plant growth. Both stress treatments reduced maximum and diurnal net photosynthesis (A) but resulted in different physiological or biochemical adjustments that tended to maintain or increase A per unit of resource (nitrogen or water) in shortest supply while decreasing the ratio of A per unit of abundant resource. Nutrient-stress reduced total foliar nitrogen, foliar chlorophyll, and initial and total RuBPCase activities, thereby enhancing or preserving photosynthetic nitrogen-use efficiency (NUE), defined as the maximum A observed per unit of leaf nitrogen, relative to the control and H2O-stress treatments. In addition, N-stress reduced photosynthetic water-use efficiency (WUE), defined as the ratio of A to stomatal conductance to water vapour (g). The slope of A versus g increased with H2O-stress. In addition, sunflower plants responded to H2O-stress by accumulating foliar glucose and sucrose and by exhibiting diurnal leaf wilting, which presumably provided additional improvements in photosynthetic WUE through osmoregulation and reduction of midday radiation interception respectively. Photosynthetic NUE was decreased by H2O-stress in that control levels of total nitrogen, foliar chlorophyll, and RuBPCase activities were maintained even after mean diurnal levels of A had fallen to less than 50% of the control level. We conclude that field-grown sunflower manages a trade-off between photosynthetic WUE and NUE, increasing use efficiency of the scarce resource while decreasing use efficiency of the abundant resource.
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