H. Bassirirad et al., Root system adjustments: regulation of plant nutrient uptake and growth responses to elevated CO2, OECOLOGIA, 126(3), 2001, pp. 305-320
Nutrients such as nitrogen (N) and phosphorus (P) often limit plant growth
rate and production in natural and agricultural ecosystems. Limited availab
ility of these nutrients is also a major factor influencing longterm plant
and ecosystem responses to rising atmospheric CO2 levels, i.e., the commonl
y observed short-term increase in plant biomass may not be sustained over t
he long-term. Therefore, it is critical to obtain a mechanistic understandi
ng of whether elevated CO2 can elicit compensatory adjustments such that ac
quisition capacity for minerals increases in concert with carbon (C) uptake
. Compensatory adjustments such as increases in (a) root mycorrhizal infect
ion, (b) root-to-shoot ratio and changes in root morphology and architectur
e, (c) root nutrient absorption capacity, and (d) nutrient-use efficiency c
an enable plants to meet an increased nutrient demand under high CO2. Here
we examine the literature to assess the extent to which these mechanisms ha
ve been shown to respond to high CO2. The literature survey reveals no cons
istent pattern either in direction or magnitude of responses of these mecha
nisms to high CO2. This apparent lack of a pattern may represent variations
in experimental protocol and/or interspecific differences. We found that i
n addressing nutrient uptake responses to high CO2 most investigators have
examined these mechanisms in isolation. Because such mechanisms can potenti
ally counterbalance one another, a more reliable prediction of elevated CO2
responses requires experimental designs that integrate all mechanisms simu
ltaneously. Finally, we present a functional balance (FB) model as an examp
le of how root system adjustments and nitrogen-use efficiency can be integr
ated to assess growth responses to high CO2. The FB model suggests that the
mechanisms of increased N uptake highlighted here have different weights i
n determining overall plant responses to high CO2. For example, while chang
es in root-to-shoot biomass allocation, r, have a small effect on growth, a
djustments in uptake rate per unit root mass, <(<nu>)over bar>, and photosy
nthetic N use efficiency, p*, have a significantly greater leverage on grow
th responses to elevated CO2 except when relative growth rate (RGR) reaches
its developmental limit, maximum RGR (RGR(max)).