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  • 1
    ISSN: 1365-2486
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Geography
    Notes: Forest floor CO2 efflux (Fff) depends on vegetation type, climate, and soil physical properties. We assessed the effects of biological factors on Fff by comparing a maturing pine plantation (PP) and a nearby mature Oak-Hickory-type hardwood forest (HW). Fff was measured continuously with soil chambers connected to an IRGA during 2001–2002. At both sites, Fff depended on soil temperature at 5 cm (T5) when soil was moist (soil moisture, θ〉0.20 m3 m−3), and on both T5 and θ when soil was drier. A model (Fff (T5, θ)) explained 〈inlineGraphic alt="geqslant R: gt-or-equal, slanted" extraInfo="nonStandardEntity" href="urn:x-wiley:13541013:GCB915:ges" location="ges.gif"/〉92% of the variation in the daily mean Fff at both sites. Higher radiation reaching the ground during the leafless period, and a thinner litter layer because of faster decomposition, probably caused higher soil temperature at HW compared with PP. The annual Fff was estimated at 1330 and 1464 g C m−2 yr−1 for a year with mild drought (2001) at PP and HW, respectively, and 1231 and 1557 g C m−2 yr−1 for a year with severe drought (2002). In the wetter year, higher soil temperature and moisture at HW compared with PP compensated for the negative effect on Fff of the response to these variables resulting in similar annual Fff at both stands. In the drier year, however, the response to soil temperature and moisture was more similar at the two stands causing the difference in the state variables to impel a higher Fff at HW. A simple mass balance indicated that in the wetter year, C in the litter–soil system was at steady state at HW, and was accruing at PP. However, HW was probably losing C from the mineral soil during the severe drought year of 2002, while PP was accumulating C at a lower rate because of a loss of C from the litter layer. Such contrasting behavior of two forest types in close proximity might frustrate attempts to estimate regional carbon (C) fluxes and net C exchange.
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Plant, cell & environment 23 (2000), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Variation in stomatal conductance is typically explained in relation to environmental conditions. However, tree height may also contribute to the variability in mean stomatal conductance. Mean canopy stomatal conductance of individual tree crowns (GSi) was estimated using sap flux measurements in Fagus sylvatica L., and the hypothesis that GSi decreases with tree height was tested. Over 13 d of the growing season during which soil moisture was not limiting, GSi decreased linearly with the natural logarithm of vapour pressure deficit (D), and increased exponentially to saturation with photosynthetic photon flux density (Qo). Under conditions of D= 1 kPa and saturating Qo, GSi decreased by approximately 60% with 30 m increase in tree height. Over the same range in height, sapwood-to-leaf area ratio (AS:AL) doubled. A simple hydraulic model explained the variation in GSi based on an inverse relationship with height, and a linear relationship with AS:AL. Thus, in F. sylvatica, adjustments in AS:AL partially compensate for the negative effect of increased flow-path length on leaf conductance. Furthermore, because stomata with low conductance are less sensitive to D, gas exchange of tall trees is reduced less by high D. Despite these compensations, decreasing hydraulic conductance with tree height in F. sylvatica reduces carbon uptake through a corresponding decrease in stomatal conductance.
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  • 3
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Responses of stomatal conductance (gs) to increasing vapour pressure deficit (D) generally follow an exponential decrease described equally well by several empirical functions. However, the magnitude of the decrease – the stomatal sensitivity – varies considerably both within and between species. Here we analysed data from a variety of sources employing both porometric and sap flux estimates of gs to evaluate the hypothesis that stomatal sensitivity is proportional to the magnitude of gs at low D (≤ 1 kPa). To test this relationship we used the function gs=gsref–m· lnD where m is the stomatal sensitivity and gsref=gs at D= 1 kPa. Regardless of species or methodology, m was highly correlated with gsref (average r2= 0·75) with a slope of approximately 0·6. We demonstrate that this empirical slope is consistent with the theoretical slope derived from a simple hydraulic model that assumes stomatal regulation of leaf water potential. The theoretical slope is robust to deviations from underlying assumptions and variation in model parameters. The relationships within and among species are close to theoretical predictions, regardless of whether the analysis is based on porometric measurements of gs in relation to leaf-surface D (Ds), or on sap flux-based stomatal conductance of whole trees (GSi), or stand-level stomatal conductance (GS) in relation to D. Thus, individuals, species, and stands with high stomatal conductance at low D show a greater sensitivity to D, as required by the role of stomata in regulating leaf water potential.
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Plant, cell & environment 23 (2000), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: We investigated the hydraulic consequences of a major decrease in root-to-leaf area ratio (AR:AL) caused by nutrient amendments to 15-year-old Pinus taeda L. stands on sandy soil. In theory, such a reduction in AR:AL should compromise the trees’ ability to extract water from drying sand. Under equally high soil moisture, canopy stomatal conductance (GS) of fertilized trees (F) was 50% that of irrigated/fertilized trees (IF), irrigated trees (I), and untreated control trees (C). As predicted from theory, F trees also decreased their stomatal sensitivity to vapour pressure deficit by 50%. The lower GS in F was associated with 50% reduction in leaf-specific hydraulic conductance (KL) compared with other treatments. The lower KL in F was in turn a result of a higher leaf area per sapwood area and a lower specific conductivity (conducting efficiency) of the plant and its root xylem. The root xylem of F trees was also 50% more resistant to cavitation than the other treatments. A transport model predicted that the lower AR:AL in IF trees resulted in a considerably restricted ability to extract water during drought. However, this deficiency was not exposed because irrigation minimized drought. In contrast, the lower AR:AL in F trees caused only a limited restriction in water extraction during drought owing to the more cavitation resistant root xylem in this treatment. In both fertilized treatments, approximate safety margins from predicted hydraulic failure were minimal suggesting increased vulnerability to drought-induced dieback compared with non-fertilized trees. However, IF trees are likely to be so affected even under a mild drought if irrigation is withheld.
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  • 5
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Using a combination of model simulations and detailed measurements at a hierarchy of scales conducted at a sandhills forest site, the effect of fertilization on net ecosystem exchange (NEE) and its components in 6-year-old Pinus taeda stands was quantified. The detailed measurements, collected over a 20-d period in September and October, included gas exchange and eddy covariance fluxes, sampled for a 10-d period each at the fertilized stand and at the control stand. Respiration from the forest floor and above-ground biomass was measured using chambers during the experiment. Fertilization doubled leaf area index (LAI) and increased leaf carboxylation capacity by 20%. However, this increase in total LAI translated into an increase of only 25% in modelled sunlit LAI and in canopy photosynthesis. It is shown that the same climatic and environmental conditions that enhance photosynthesis in the September and October periods also cause an increase in respiration The increases in respiration counterbalanced photosynthesis and resulted in negligible NEE differences between fertilized and control stands. The fact that total biomass of the fertilized stand exceeded 2·5 times that of the control, suggests that the counteracting effects cannot persist throughout the year. In fact, modelled annual carbon balance showed that gross primary productivity (GPP) increased by about 50% and that the largest enhancement in NEE occurred in the spring and autumn, during which cooler temperatures reduced respiration more than photosynthesis. The modelled difference in annual NEE between fertilized  and  control  stands  (approximately  200 1;g 2;C 3;m−2 y−1)  suggest that the effect of fertilization was sufficiently large to transform the stand from a net terrestrial carbon source to a net sink.
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  • 6
    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: Many aspects of plant water use – particularly in response to soil drought – may have as their basis the alteration of hydraulic conductance from soil to canopy. The regulation of plant water potential (Ψ) by stomatal control and leaf area adjustment may be necessary to maximize water uptake on the one hand, while avoiding loss of hydraulic contact with the soil water on the other. Modelling the changes in hydraulic conductance with pressure gradients in the continuum allows the prediction of water use as a function of soil environment and plant architectural and xylem traits. Large differences in water use between species can be attributed in part to differences in their ‘hydraulic equipment’ that is presumably optimized for drawing water from a particular temporal and spatial niche in the soil environment. A number of studies have identified hydraulic limits as the cause of partial or complete foliar dieback in response to drought. The interactions between root:shoot ratio, rooting depth, xylem properties, and soil properties in influencing the limits to canopy water supply can be used to predict which combinations should optimize water use in a given circumstance. The hydraulic approach can improve our understanding of the coupling of canopy processes to soil environment, and the adaptive significance of stomatal behaviour.
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