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  • CO2 assimilation  (1)
  • Carbon uptake  (1)
  • Spruce (Picea abies)  (1)
  • Storage
  • Springer  (3)
  • 1995-1999
  • 1985-1989  (3)
  • 1988  (3)
Collection
Keywords
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  • Springer  (3)
Years
  • 1995-1999
  • 1985-1989  (3)
Year
  • 1
    ISSN: 1432-1939
    Keywords: CO2 assimilation ; stomatal responses ; soil drying rate ; cowpea
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Well watered plants of Vigna unguiculata (L.) Walp cv. California Blackeye No. 5 had maximum photosynthetic rates of 16 μmol m-2 s-1 (at ambient CO2 concentration and environmental parameters optimal for high CO2 uptake). Leaf conductance declined with increasing water vapour concentration difference between leaf and air (Δw), but it increased with increasing leaf temperature at a constant small Δw. When light was varied, CO2 assimilation and leaf conductance were correlated linearly. We tested the hypothesis that g was controlled by photosynthesis via intercellular CO2 concentration (c i). No unique relationship between (1) c i, (2) the difference between ambient CO2 concentration (c a) and c i, namely c a-c i, or (3) the c i/c a ratio and g was found. g and A appeared to respond to environmental factors fairly independently of each other. The effects of different rates of soil drying on leaf gas exchange were studied. At unchanged air humidity, different rates of soil drying were produced by using (a) different soils, (b) different irrigation schemes and (c) different soil volumes per plant. Although the soil dried to wilting point the relative leaf water content was little affected. Different soil drying rates always resulted in the same response of photosynthetic capacity (A max) and corresponding leaf conductance (g(Amax)) when plotted against percent relative plant-extractable soil water content (W e %) but the relationship with relative soil water content (W e ) was less clear. Above a range of W e of 15%–25%, A max and g(Amax) were both high and responded little to decreasing W e . As soon as W e fell below this range, A max and g(Amax) declined. The data suggest root-to-leaf communication not mediated via relative leaf water content. However, g(Amax) was initially more affected than A max.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Oecologia 77 (1988), S. 163-173 
    ISSN: 1432-1939
    Keywords: Forest decline ; Spruce (Picea abies) ; Nutrients ; Growth
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary A declining, closed-canopy Picea abies (L.) Karst. stand produced as much crown biomass as a healthy stand, although some trees were chlorotic due to magnesium deficiency. The production of wood per unit of leaf area in both stands was related to the foliar magnesium concentration. Although leaf area index and climate were similar at both sites, stemwood production was 35% lower in the declining than in the healthy stand. Nutritional disharmony, rather than a deficiency in a single element, was identified as the mechanism for reduced tree vigor. The role of nutrient stress in forest decline was detected by partitioning the season into three periods reflecting different phenological stages: a canopy growth period in spring, a stem growth period in summer, and a recharge period during the non-growing season. Needle growth was associated with nitrogen supply. Most of the magnesium supply required to meet the demand for foliage growth was retranslocated from mature needles. Magnesium retranslocation was related to concentration of nitrogen and magnesium in those needles before bud break. Retranslocation from mature needles during the phase of canopy production resulted in chlorosis in initially green needles if the magnesium concentration before bud break was low. Nitrogen concentration in 0-year-old needles generally remained constant with increasing supply, indicating that foliage growth was restricted by the supply of nitrogen. In contrast, magnesium concentration generally increased with supply, indicating that magnesium supply for needle growth was sufficient. Much of the magnesium required for wood production was taken up from the soil because stored magnesium was largely used for canopy growth. Uptake at the declining site was probably limited because of restricted root expansion and lower soil magnesium compared to the healthy site. For this reason only wood growth was reduced at the declining site. Because the recharge of magnesium during the non-growing period is dependent on uptake from the soil, it was more limited at the declining that at the healthy stand. However, as nitrogen uptake from the atmosphere may account for an appreciable proportion of the total uptake, and as its supply in the soil at both sites was similar, an unbalanced recharge of nitrogen and magnesium may have occurred at the declining site. If mature needles are unable to recharge with magnesium in proportion to the uptake of nitrogen, chlorosis is likely to occur during the next canopy growth period.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Trees 2 (1988), S. 233-241 
    ISSN: 1432-2285
    Keywords: Larix ; Carbon uptake ; Respiration ; Carbon balances ; Water loss ; Sun and shade branches
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Shade needles of hybrid larch (Larix decidua × leptolepis) had the same rates of photosynthesis as sun needles per dry weight and nitrogen, and a similar leaf conductance under conditions of light saturation at ambient CO2 (Amax). However, on an area basis, Amax and specific leaf weight were lower in shade than in sun needles. Stomata of sun needles limited CO2 uptake at light saturation by about 20%, but under natural conditions of light in the shade crown, shade needles operated in a range of saturating internal CO2 without stomatal limitation of CO2 uptake. In both needle types, stomata responded similarly to changes in light, but shade needles were more sensitive to changes in vapor pressure deficit than sun needles. Despite a high photosynthetic capacity, the ambient light conditions reduced the mean daily (in summer) and annual carbon gain of shade needles to less than 50% of that in sun needles. In sun needles, the transpiration per carbon gain was about 220 mol mol−1 on an annual basis. The carbon budget of branches was determined from the photosynthetic rate, the needle biomass and respiration, the latter of which was (per growth and on a carbon basis) 1.6 mol mol−1 year−1 in branch and stem wood. In shade branches carbon gains exceeded carbon costs (growth + respiration) by only a factor of 1.6 compared with 3.5 in sun branches. The carbon balance of sun branches was 5 times higher per needle biomass of a branch or 9 times higher on a branch length basis than shade branches. The shade foliage (including the shaded near-stem sun foliage) only contributed approximately 23% to the total annual carbon gain of the tree.
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