Once forests have achieved a full canopy, their growth rate declines progressively with age. This work used a global data set with estimates from a wide range of forest types, aged 20-795 years, of their annual photos...Once forests have achieved a full canopy, their growth rate declines progressively with age. This work used a global data set with estimates from a wide range of forest types, aged 20-795 years, of their annual photosynthetic production(gross primary production, GPP) and subsequent above-plus below-ground biomass production(net primary production, NPP). Both GPP and NPP increased with increasing mean annual temperature and precipitation. GPP was then unrelated to forest age whilst NPP declined progressively with increasing age. These results implied that autotrophic respiration increases with age. It has been proposed that GPP should decline in response to increasing water stress in leaves as water is raised to greater heights as trees grow taller with age. However, trees may make substantial plastic adjustment in mor phology and anatomy of newly developing leaves, xylem and fi ne roots to compensate for this stress and maintain GPP with age. This work reviews the possibilities that NPP declines with age as respiratory costsincrease progressively in, any or all of, the construction and maintenance of more complex tissues, the maintenance of increasing amounts of live tissue within the sapwood of stems and coarse roots, the conversion of sapwood to hear twood, the increasing distance of phloem transport, increased turnover rates of fine roots, cost of supporting very tall trees that are unable to compensate fully for increased water stress in their canopies or maintaining alive competitively unsuccessful small trees.展开更多
In forest growing at any one site, the growth rate of an individual tree is determined principally by its size, which reflects its metabolic capacity, and by competition from neighboring trees. Competitive effects of ...In forest growing at any one site, the growth rate of an individual tree is determined principally by its size, which reflects its metabolic capacity, and by competition from neighboring trees. Competitive effects of a tree may be proportional to its size;such competition is termed ‘sym-metric’ and generally involves competition below ground for nutrients and water from the soil. Competition may also be ‘asymmetric’, where its effects are disproportionate to the size of the tree;this generally involves competition above ground for sunlight, when larger trees shade smaller, but the reverse cannot occur. This work examines three model systems often seen as exemplars relating individual tree growth rates to tree size and both competitive processes. Data of tree stem basal area growth rates in plots of even- aged, monoculture forest of blackbutt (Eucalyptus pilularis Smith) growing in sub-tropical eastern Australia were used to test these systems. It was found that none could distin-guish between size and competitive effects at any time in any one stand and, thus, allow quantification of the contribution of each to explaining tree growth rates. They were prevented from doing so both by collinearity between the terms used to describe each of the effects and technical problems involved in the use of nonlinear least-squares regression to fit the models to any one data set. It is concluded that quite new approaches need to be devised if the effects on tree growth of tree size and competitive processes are to be quantified and modelled successfully.展开更多
Inventory data were available from 96 plots of even-aged,monoculture,tall-open forests of Eucalyptus pilularis Smith,aged 2-63 years,growing in sub-tropical regions along the east coast of Australia.A model was develo...Inventory data were available from 96 plots of even-aged,monoculture,tall-open forests of Eucalyptus pilularis Smith,aged 2-63 years,growing in sub-tropical regions along the east coast of Australia.A model was developed relating the maximum possible stem basal area growth rate of individual trees to their stem basal area.For any tree size,this maximum increased as site productivity increased.However,the size at which this maximum occurred decreased as productivity increased.Much research has shown that,at any stand age,trees of a particular stem basal area are taller on more productive sites than on less productive ones.Taller trees incur greater respiratory costs to ensure maintenance of the photo synthetic capacity of their canopies;this reduces their growth rates.It was concluded that trees with larger basal areas will have the maximum possible growth rate on a less productive site,whilst trees with smaller basal areas will have the maximum possible on a more productive site.The model developed may constitute the first stage of a complete individual tree growth model system to predict wood yields from these forests.展开更多
文摘Once forests have achieved a full canopy, their growth rate declines progressively with age. This work used a global data set with estimates from a wide range of forest types, aged 20-795 years, of their annual photosynthetic production(gross primary production, GPP) and subsequent above-plus below-ground biomass production(net primary production, NPP). Both GPP and NPP increased with increasing mean annual temperature and precipitation. GPP was then unrelated to forest age whilst NPP declined progressively with increasing age. These results implied that autotrophic respiration increases with age. It has been proposed that GPP should decline in response to increasing water stress in leaves as water is raised to greater heights as trees grow taller with age. However, trees may make substantial plastic adjustment in mor phology and anatomy of newly developing leaves, xylem and fi ne roots to compensate for this stress and maintain GPP with age. This work reviews the possibilities that NPP declines with age as respiratory costsincrease progressively in, any or all of, the construction and maintenance of more complex tissues, the maintenance of increasing amounts of live tissue within the sapwood of stems and coarse roots, the conversion of sapwood to hear twood, the increasing distance of phloem transport, increased turnover rates of fine roots, cost of supporting very tall trees that are unable to compensate fully for increased water stress in their canopies or maintaining alive competitively unsuccessful small trees.
文摘In forest growing at any one site, the growth rate of an individual tree is determined principally by its size, which reflects its metabolic capacity, and by competition from neighboring trees. Competitive effects of a tree may be proportional to its size;such competition is termed ‘sym-metric’ and generally involves competition below ground for nutrients and water from the soil. Competition may also be ‘asymmetric’, where its effects are disproportionate to the size of the tree;this generally involves competition above ground for sunlight, when larger trees shade smaller, but the reverse cannot occur. This work examines three model systems often seen as exemplars relating individual tree growth rates to tree size and both competitive processes. Data of tree stem basal area growth rates in plots of even- aged, monoculture forest of blackbutt (Eucalyptus pilularis Smith) growing in sub-tropical eastern Australia were used to test these systems. It was found that none could distin-guish between size and competitive effects at any time in any one stand and, thus, allow quantification of the contribution of each to explaining tree growth rates. They were prevented from doing so both by collinearity between the terms used to describe each of the effects and technical problems involved in the use of nonlinear least-squares regression to fit the models to any one data set. It is concluded that quite new approaches need to be devised if the effects on tree growth of tree size and competitive processes are to be quantified and modelled successfully.
文摘Inventory data were available from 96 plots of even-aged,monoculture,tall-open forests of Eucalyptus pilularis Smith,aged 2-63 years,growing in sub-tropical regions along the east coast of Australia.A model was developed relating the maximum possible stem basal area growth rate of individual trees to their stem basal area.For any tree size,this maximum increased as site productivity increased.However,the size at which this maximum occurred decreased as productivity increased.Much research has shown that,at any stand age,trees of a particular stem basal area are taller on more productive sites than on less productive ones.Taller trees incur greater respiratory costs to ensure maintenance of the photo synthetic capacity of their canopies;this reduces their growth rates.It was concluded that trees with larger basal areas will have the maximum possible growth rate on a less productive site,whilst trees with smaller basal areas will have the maximum possible on a more productive site.The model developed may constitute the first stage of a complete individual tree growth model system to predict wood yields from these forests.
