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  • 1
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    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.
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  • 2
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    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.
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Plant, cell & environment 19 (1996), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: We studied the effects of variations of water flux through the plant, of diurnal variation of water flux, and of variation of vapour pressure deficit at the leaf on compensation pressure in the Passioura-type pressure chamber, the composition of the xylem sap and leaf conductance in Ricinus communis. The diurnal pattern of compensation pressure showed stress relaxation during the night hours, while stress increased during the day, when water limitation increased. Thus compensation pressure was a good measure of the momentary water status of the root throughout the day and during drought. The bulk soil water content at which predawn compensation pressure and abscisic acid concentration in the xylem sap increased and leaf conductance decreased, was high when the water usage of the plant was high. For all xylem sap constituents analysed, variations in concentrations during the day were larger than changes in mean concentrations with drought. Mean concentrations of phosphate and the pH of the xylem sap declined with drought, while nitrate concentration remained constant. When the measurement leaf was exposed to a different VPD from the rest of the plant, leaf conductance declined by 400mmol m−2 s−1 when compensation pressure increased by 1 MPa in all treatments. The compensation pressure needed to keep the shoot turgid, leaf conductance and the abscisic acid concentration in the xylem were linearly related. This was also the case when the highly dynamic development of stress was taken into account.
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  • 4
    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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  • 5
    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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  • 6
    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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  • 7
    ISSN: 1432-1939
    Keywords: C4 photosynthesis ; δ13C values ; Grass flora of Namibia ; Poaceae ; Geographic distribution
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The grass flora of Namibia (374 species in 110 genera) shows surprisingly little variation in δ13C values along a rainfall gradient (50–600 mm) and in different habitat conditions. However, there are significant differences in the δ13C values between the metabolic types of the C4 photosynthetic pathway. NADP-ME-type C4 species exhibit the highest δ13C values (−11.7 ‰) and occur mainly in regions with high rainfall. NAD-ME-type C4 species have significantly lower δ13C values (−13.4 ‰) and dominate in the most arid part of the precipitation regime. PCK-type C4 species play an intermediate role (−12.5 ‰) and reach a maximum abundance in areas of intermediate precipitation. This pattern is also evident in genera containing species of different metabolic types. Within the same genus NAD species reach more negative δ13C values than PCK species and δ13C values decreased with rainfall. Also in Aristida, with NADP-ME-type photosynthesis, δ13C values decreased from −11 ‰ in the inland region (600 mm precipitation) to −15 ‰ near the coast (150 mm precipitation), which is a change in discrimination which is otherwise associated by a change in metabolism. The exceptional C3 species Eragrostis walteri and Panicum heterostachyum are coastal species experiencing 50 mm precipitation only. Many of the rare species and monotypic genera grow in moist habitats rather than in the desert, and they are not different in their carbon isotope ratios from the more common flora. The role of species diversity with respect to habitat occupation and carbon metabolism is discussed.
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  • 8
    ISSN: 1432-1939
    Keywords: Storage ; Accumulation ; Reserve formation ; Storage structure ; Biennial plants
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Four biennial species (Arctium tomentosum, Cirsium vulgare, Dipsacus sylvester and Daucus carota) which originate from habitats of different nutrient availability were investigated in a 2-year experiment in a twofactorial structured block design varying light (natural daylight versus shading) and fertilizer addition. The experiment was designed to study storage as reserve formation (competing with growth) or as accumulation (see Chapin et al. 1990). We show that (i) the previous definitions of storage excluded an important process, namely the formation of storage tissue. Depending on species, storage tissue and the filling process can be either a process of reserve formation, or a process of accumulation. (ii) In species representing low-resource habitats, the formation of a storage structure competes with other growth processes. Growth of storage tissue and filling with storage products is an accumulation process only in the high-resource plant Arctium tomentosum. We interpret the structural growth of low-resource plants in terms of the evolutionary history of these species, which have closely related woody species in the Mediterranean area. (iii) The use of storage products for early leaf growth determines the biomass development in the second season and the competitive ability of this species during growth with perennial species. (iv) The high-resource plant Arctium has higher biomass development under all conditions, i.e. plants of low-resource habitats are not superior under low-resource conditions. The main difference between high- and low-resource plants is that low-resource plants initiate flowering at a lower total plant internal pool size of available resources.
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  • 9
    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.
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  • 10
    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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