The scaling of respiratory metabolism with body mass is one of the most pervasive phenomena in biology. Using a single allometric equation to characterize empirical scaling relationships and to evaluate alternative hypotheses about mechanisms has been controversial. We developed a method to directly measure respiration of 271 whole plants, spanning nine orders of magnitude in body mass, from small seedlings to large trees, and from tropical to boreal ecosystems. Our measurements include the roots, which have often been ignored. Rather than a single power-law relationship, our data are fit by a biphasic, mixed-power function. The allometric exponent varies continuously from 1 in the smallest plants to 3/4 in larger saplings and trees. The transition from linear to 3/4-power scaling may indicate fundamental physical and physiological constraints on the allocation of plant biomass between photosynthetic and nonphotosynthetic organs over the course of ontogenetic plant growth.allometry | metabolic scaling | mixed-power function | whole-plant respiration | simple-power function F rom the smallest seedlings to giant trees, the masses of vascular plants span 12 orders of magnitude in mass (1). The growth rates of most plants, which are generally presented in terms of net assimilation rates of CO 2 , are believed to be controlled by respiration (2, 3). Furthermore, many of the CO 2 -budget models of plant growth and carbon dynamics in terrestrial ecosystems are based on whole-plant respiration rates in relation to plant size (2, 4-7). Thus far, however, there have been few studies of wholeplant respiration over the entire range of plant size from tiny seedlings to large trees. The purpose of the present study was to quantify the allometric scaling of metabolism by directly measuring whole-plant respiration over a representative range of sizes.For the past century, the scaling of metabolic rate with body size has usually been described using an allometric equation, or simple power function, for the form (8-17)where Y is the respiratory metabolic rate (μmol s −1 ), F is a constant (μmol s −1 kg -f ), M is the body mass (kg), and f is the scaling exponent. The exponent f has been controversial, and various values have been reported based on studies of both animals and plants (15). Recently, it was suggested that f = 1 for relatively small plants, based on data for a 10 6 -fold range of body mass (16), including measurements using a whole-plant chamber (18,19). If f = 1, this means that whole-plant respiration scales isometrically with body mass, which may be reasonable in the case of herbaceous plants and small trees because nearly all of their cells, even those in the stems, should be active in respiration. However, it was suggested that f = 3/4 based originally on empirical studies of animal metabolism (8). This idea is consistent with the mechanistic models of resource distribution in vascular systems (10, 11), including the pipe model (20, 21) and models based on space-filling, hierarchical, fractal-like networks of br...
We assessed above- and belowground biomass and net primary production (NPP) of a mature Larix gmelinii (Rupr.) Rupr. forest (240-280 years old) established on permafrost soils in central Siberia. Specifically, we investigated annual carbon budgets in roots in relation to root system development and availability of soil resources. Total stand biomass estimated by allometry was about 39 Mg per ha. Root biomass (17 Mg per ha) comprised about 43% of total biomass. Coarse root (>/= 5 mm in diameter) biomass was about twice that of fine roots (< 5 mm). The aboveground biomass/root biomass ratio (T/R) of the larch stand was about unity, which is much less than that of other boreal and subalpine conifer forests. The proportion of fine roots in total root biomass (35%) was relatively high compared with other cold-climate evergreen conifer forests. Total NPP, defined as the sum of annual biomass increment of woody parts and needle biomass, was estimated to be 1.8 Mg per ha per year. Allocation of total NPP to needle production was 56%. The proportion of total NPP in belowground production (27%) was less than for evergreen taiga forests. However, belowground NPP was probably under-estimated because root mortality was excluded. We conclude that L. gmelinii trees invested annual carbon gains largely into needle production or roots, or both, at the expense of growth of aboveground woody parts. This carbon allocation pattern, which resulted in the construction of exploitative root networks, appeared to be a positive growth response to the nutrient-poor permafrost soil of central Siberia.
We compared effects of ambient (360 vpm) and elevated (720 vpm) carbon dioxide concentration ([CO2]) and high and low nutrient supply rates on stem growth, annual ring structure and tracheid anatomy of Siberian larch (Larix sibirica Ledeb.) seedlings over two growing seasons. Elevated [CO2] had no significant effect on either stem height or diameter growth; however, both stem height and diameter growth were enhanced by the high nutrient supply rate, and these increases were stimulated by elevated [CO2]. Elevated [CO2] tended to increase the width of the annual xylem ring, the number of cells in a radial file spanning the ring, and tracheid lumen diameter, whereas it tended to reduce cell wall thickness, although there were no statistically significant CO2 effects on tracheid anatomy. Changes in tracheid cell morphology seemed to be dependent on changes in shoot elongation rates.
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