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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Inorganic chemistry 10 (1971), S. 1453-1457 
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Plant, cell & environment 26 (2003), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: In the present study the response of stomatal conductance (gs) to increasing leaf-to-air vapour pressure difference (D) in early season C3 (Bromus japonicus) and late season C4 (Bothriochloa ischaemum) grasses grown in the field across a range of CO2 (200–550 µmol mol−1) was examined. Stomatal sensitivity to D was calculated as the slope of the response of gs to the natural log of externally manipulated D (dgs/dlnD). Increasing D and CO2 significantly reduced gs in both species. Increasing CO2 caused a significant decrease in stomatal sensitivity to D in Br. japonicus, but not in Bo. ischaemum. The decrease in stomatal sensitivity to D at high CO2 for Br. japonicus fit theoretical expectations of a hydraulic model of stomatal regulation, in which gs varies to maintain constant transpiration and leaf water potential. The weaker stomatal sensitivity to D in Bo. ischaemum suggested that stomatal regulation of leaf water potential was poor in this species, or that non-hydraulic signals influenced guard cell behaviour. Photosynthesis (A) declined with increasing D in both species, but analyses of the ratio of intercellular to atmospheric CO2 (Ci/Ca) suggested that stomatal limitation of A occurred only in Br. japonicus. Rising CO2 had the greatest effect on gs and A in Br. japonicus at low D. In contrast, the strength of stomatal and photosynthetic responses to CO2 were not affected by D in Bo. ischaemum. Carbon and water dynamics in this grassland are dominated by a seasonal transition from C3 to C4 photosynthesis. Interspecific variation in the response of gs to D therefore has implications for predicting seasonal ecosystem responses to CO2.
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  • 3
    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.
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science, Ltd
    Plant, cell & environment 25 (2002), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: An investigation to determine whether stomatal acclimation to [CO2] occurred in C3/C4 grassland plants grown across a range of [CO2] (200–550 µmol mol−1) in the field was carried out. Acclimation was assessed by measuring the response of stomatal conductance (gs) to a range of intercellular CO2 (a gs–Ci curve) at each growth [CO2] in the third and fourth growing seasons of the treatment. The gs–Ci response curves for Solanum dimidiatum (C3 perennial forb) differed significantly across [CO2] treatments, suggesting that stomatal acclimation had occurred. Evidence of non–linear stomatal acclimation to [CO2] in this species was also found as maximum gs (gsmax; gs measured at the lowest Ci) increased with decreasing growth [CO2] only below 400 µmol mol−1. The substantial increase in gs at subambient [CO2] for S. dimidiatum was weakly correlated with the maximum velocity of carboxylation (Vcmax; r2 = 0·27) and was not associated with CO2 saturated photosynthesis (Amax). The response of gs to Ci did not vary with growth [CO2] in Bromus japonicus (C3 annual grass) or Bothriochloa ischaemum (C4 perennial grass), suggesting that stomatal acclimation had not occurred in these species. Stomatal density, which increased with rising [CO2] in both C3 species, was not correlated with gs. Larger stomatal size at subambient [CO2], however, may be associated with stomatal acclimation in S. dimidiatum. Incorporating stomatal acclimation into modelling studies could improve the ability to predict changes in ecosystem water fluxes and water availability with rising CO2 and to understand their magnitudes relative to the past.
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  • 5
    ISSN: 1435-0629
    Keywords: Key words: biosphere metabolism; carbon cycle; carbon fluxes; global change; terrestrial ecosystems.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: ABSTRACT Understanding terrestrial carbon metabolism is critical because terrestrial ecosystems play a major role in the global carbon cycle. Furthermore, humans have severely disrupted the carbon cycle in ways that will alter the climate system and directly affect terrestrial metabolism. Changes in terrestrial metabolism may well be as important an indicator of global change as the changing temperature signal. Improving our understanding of the carbon cycle at various spatial and temporal scales will require the integration of multiple, complementary and independent methods that are used by different research communities. Tools such as air sampling networks, inverse numerical methods, and satellite data (top-down approaches) allow us to study the strength and location of the global- and continental-scale carbon sources and sinks. Bottom-up studies provide estimates of carbon fluxes at finer spatial scales and examine the mechanisms that control fluxes at the ecosystem, landscape, and regional scales. Bottom-up approaches include comparative and process studies (for example, ecosystem manipulative experiments) that provide the necessary mechanistic information to develop and validate terrestrial biospheric models. An iteration and reiteration of top-down and bottom-up approaches will be necessary to help constrain measurements at various scales. We propose a major international effort to coordinate and lead research programs of global scope of the carbon cycle.
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  • 6
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 344 (1990), S. 58-60 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 7
    ISSN: 1432-1939
    Keywords: Patagonia-vegetation ; Root distribution ; 13C-, 18O-, D-Isotope composition ; Water ; Plant succession
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Above-and belowground biomass distribution, isotopic composition of soil and xylem water, and carbon isotope ratios were studied along an aridity gradient in Patagonia (44–45°S). Sites, ranging from those with Nothofagus forest with high annual rainfall (770 mm) to Nothofagus scrub (520 mm), Festuca (290 mm) and Stipa (160 mm) grasslands and into desert vegetation (125 mm), were chosen to test whether rooting depth compensates for low rainfall. Along this gradient, both mean above-and belowground biomass and leaf area index decreased, but average carbon isotope ratios of sun leaves remained constant (at-27‰), indicating no major differences in the ratio of assimilation to stomatal conductance at the time of leaf growth. The depth of the soil horizon that contained 90% of the root biomass was similar for forests and grasslands (about 0.80–0.50 m), but was shallower in the desert (0.30 m). In all habitats, roots reached water-saturated soils or ground water at 2–3 m depth. The depth profile of oxygen and hydrogen isotope ratios of soil water corresponded inversely to volumetric soil water contents and showed distinct patterns throughout the soil profile due to evaporation, water uptake and rainfall events of the past year. The isotope ratios of soil water indicated that high soil moisture at 2–3 m soil depth had originated from rainy periods earlier in the season or even from past rainy seasons. Hydrogen and oxygen isotope ratios of xylem water revealed that all plants used water from recent rain events in the topsoil and not from water-saturated soils at greater depth. However, this study cannot explain the vegetation zonation along the transect on the basis of water supply to the existing plant cover. Although water was accessible to roots in deeper soil layers in all habitats, as demonstrated by high soil moisture, earlier rain events were not fully utilized by the current plant cover during summer drought. The role of seedling establishment in determining species composition and vegetation type, and the indirect effect of seedling establishment on the use of water by fully developed plant cover, are discussed in relation to climate change and vegetation modelling.
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  • 8
    ISSN: 1432-1939
    Keywords: Deep roots function ; Terrestrial vegetation ; Biomes ; Plant forms ; Root depth
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The depth at which plants are able to grow roots has important implications for the whole ecosystem hydrological balance, as well as for carbon and nutrient cycling. Here we summarize what we know about the maximum rooting depth of species belonging to the major terrestrial biomes. We found 290 observations of maximum rooting depth in the literature which covered 253 woody and herbaceous species. Maximum rooting depth ranged from 0.3 m for some tundra species to 68 m for Boscia albitrunca in the central Kalahari; 194 species had roots at least 2 m deep, 50 species had roots at a depth of 5 m or more, and 22 species had roots as deep as 10 m or more. The average for the globe was 4.6±0.5 m. Maximum rooting depth by biome was 2.0±0.3 m for boreal forest. 2.1±0.2 m for cropland, 9.5±2.4 m for desert, 5.2±0.8 m for sclerophyllous shrubland and forest, 3.9±0.4 m for temperate coniferous forest, 2.9±0.2 m for temperate deciduous forest, 2.6±0.2 m for temperate grassland, 3.7±0.5 m for tropical deciduous forest, 7.3±2.8 m for tropical evergreen forest, 15.0±5.4 m for tropical grassland/savanna, and 0.5±0.1 m for tundra. Grouping all the species across biomes (except croplands) by three basic functional groups: trees, shrubs, and herbaceous plants, the maximum rooting depth was 7.0±1.2 m for trees, 5.1±0.8 m for shrubs, and 2.6±0.1 m for herbaceous plants. These data show that deep root habits are quite common in woody and herbaceous species across most of the terrestrial biomes, far deeper than the traditional view has held up to now. This finding has important implications for a better understanding of ecosystem function and its application in developing ecosystem models.
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  • 9
    ISSN: 1432-1939
    Keywords: Key words Drainage ; Ecosystem water budget ; Leaf area index ; Soil evaporation ; Plant transpiration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The need to combine data from CO2 field experiments with climate data remains urgent, particularly because each CO2 experiment cannot run for decades to centuries. Furthermore, predictions for a given biome need to take into account differences in productivity and leaf area index (LAI) independent of CO2-derived changes. In this study, we use long-term weather records and field data from the Jasper Ridge CO2 experiment in Palo Alto, California, to model the effects of CO2 and climate variability on ecosystem water fluxes. The sandstone and serpentine grasslands at Jasper Ridge provide a range of primary productivity and LAI, with the sandstone as the more productive system. Modeled soil water availability agreed well with published observations of time-domain reflectometry in the CO2 experiment. Simulated water fluxes based on 10-year weather data (January 1985–December 1994) showed that the sandstone grassland had a much greater proportion of water movement through plants than did the serpentine; transpiration accounted for approximately 30% of annual fluxes in the sandstone and only 10% in the serpentine. Although simulated physiological and biomass changes were similar in both grasslands, the consequences of elevated CO2 were greater for the sandstone water budget. Elevated CO2 increased soil drainage by 20% in the sandstone, despite an approximately one-fifth increase in plant biomass; in the serpentine, drainage increased by 〈10% and soil evaporation was unchanged for the same simulated biomass change. Phenological changes, simulated by a 15-day lengthening of the growing season, had minimal impacts on the water budget. Annual variation in the timing and amount of rainfall was important for water fluxes in both grasslands. Elevated CO2 increased sandstone drainage 〉50 mm in seven of ten years, but the relative increase in drainage varied from 10% to 300% depending on the year. Early-season transpiration in the sandstone decreased between 26% and 41%, with elevated CO2 resulting in a simulated water savings of 54–76 mm. Even in years when precipitation was similar (e.g., 505 and 479 mm in years 3 and 4), the effect of CO2 varied dramatically. The response of grassland water budgets to CO2 depends on the productivity and structure of the grassland, the amount and timing of rainfall, and CO2-induced changes in physiology. In systems with low LAI, large physiological changes may not necessarily alter total ecosystem water budgets dramatically.
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  • 10
    ISSN: 1432-1939
    Keywords: Terrestrial biomes ; Cumulative root fraction ; Root biomass ; Rooting density ; Soil depth
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Understanding and predicting ecosystem functioning (e.g., carbon and water fluxes) and the role of soils in carbon storage requires an accurate assessment of plant rooting distributions. Here, in a comprehensive literature synthesis, we analyze rooting patterns for terrestrial biomes and compare distributions for various plant functional groups. We compiled a database of 250 root studies, subdividing suitable results into 11 biomes, and fitted the depth coefficient β to the data for each biome (Gale and Grigal 1987). β is a simple numerical index of rooting distribution based on the asymptotic equation Y=1-βd, where d = depth and Y = the proportion of roots from the surface to depth d. High values of β correspond to a greater proportion of roots with depth. Tundra, boreal forest, and temperate grasslands showed the shallowest rooting profiles (β=0.913, 0.943, and 0.943, respectively), with 80–90% of roots in the top 30 cm of soil; deserts and temperate coniferous forests showed the deepest profiles (β=0.975 and 0.976, respectively) and had only 50% of their roots in the upper 30 cm. Standing root biomass varied by over an order of magnitude across biomes, from approximately 0.2 to 5 kg m-2. Tropical evergreen forests had the highest root biomass (5 kg m-2), but other forest biomes and sclerophyllous shrublands were of similar magnitude. Root biomass for croplands, deserts, tundra and grasslands was below 1.5 kg m-2. Root/shoot (R/S) ratios were highest for tundra, grasslands, and cold deserts (ranging from 4 to 7); forest ecosystems and croplands had the lowest R/S ratios (approximately 0.1 to 0.5). Comparing data across biomes for plant functional groups, grasses had 44% of their roots in the top 10 cm of soil. (β=0.952), while shrubs had only 21% in the same depth increment (β=0.978). The rooting distribution of all temperate and tropical trees was β=0.970 with 26% of roots in the top 10 cm and 60% in the top 30 cm. Overall, the globally averaged root distribution for all ecosystems was β=0.966 (r 2=0.89) with approximately 30%, 50%, and 75% of roots in the top 10 cm, 20 cm, and 40 cm, respectively. We discuss the merits and possible shortcomings of our analysis in the context of root biomass and root functioning.
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