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  • Basal area  (1)
  • Deep roots function  (1)
  • Ecosystem water budget  (1)
  • 1
    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.
    Type of Medium: Electronic Resource
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  • 2
    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.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-5052
    Keywords: Argentina ; Basal area ; Community structure ; Diversity ; Dynamics ; Flooding pampa ; Grassland ; Grazing effect ; Leaf area
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Changes in plant community structure are identified as a result of grazing in grasslands of the flooding pampa which evolved under supposedly light grazing conditions. The effect of excluding grazing upon total leaf area index was an increase of 30%. The largest response was observed in the distribution of leaves in the canopy. In the grazed areas, most of the green material was concentrated in the 0–5 cm layer while in the ungrazed treatments the largest portion of the leaf area was in the 10–30 cm layer. Grazing exclusion resulted in a small change in total basal area but a larger change in its distribution, from many small tussocks to less numerous large ones. The effect of grazing upon leaf area and basal area was accounted for by changes in vigor as well as by changes in species composition. The major effect of excluding grazing upon species composition was the disappearance of some native planophile species and most of the exotics. The species composition of grazed areas of both communities was very similar while there were large differences between the ungrazed areas and between the grazed and ungrazed areas of the same community. It is suggested that there is a group of species which responds to the coarse-grained ‘signal’ of grazing and its presence can cause dissimilar communities to converge under grazing conditions. The other group of species responded to the fine-grained ‘signal’ of the environmental conditions associated with topography.
    Type of Medium: Electronic Resource
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