RESUMO
Existing technologies for lime (CaCO3) incorporation into acidic field soils result in the heterogeneous distribution of limed and acidic soil sections. In a study characterising the response of wheat (Triticum aestivum L.) to the amendment of an acidic soil profile with vertically limed slots [1], elucidation of the dynamics of root proliferation within the acidic and limed soil sections was a prerequisite to understanding the mechanisms driving the above-ground responses. Rubidium (Rb) has been used widely as a non-radioactive tracer for root activity [2] in soil. However, the contrasting pH in a heterogeneously limed soil profile and related aluminium toxicity effects to roots can influence the availability and uptake of Rb, and quantitative data relating Rb uptake to root phenology in this scenario are lacking. To validate the use of Rb as a tracer for root activity within vertically limed slots in an acidic soil profile, its uptake by wheat roots from acidic or limed sections of subsoil, and its relation to root architecture was assessed. Wheat plants were grown in a glasshouse in 29 cm deep, vertically split soil columns with acidic (pH 3.9), Al-toxic subsoil on one side and the same soil amended with lime on the other side. Rubidium chloride was applied at 5, 10 or 20 mg Rb kg-1 to either limed or acidic soil sections. Wheat plants were grown for 28 days, after which the Rb content in shoots and the root length and diameter in each of the discrete soil sections was measured. Foremost, the Rb amendments (5, 10 or 20 mg Rb kg-1 soil) did not induce any toxic effects; shoot dry weight and root length in the limed and acidic sections of the subsoil were not statistically different among the rubidium-amended and non-amended treatments, regardless of its placement (limed vs. acidic sections). Average root lengths in the limed sections of the subsoil (69.5 m section-1) were approximately 10-fold greater than in the acidic sections (6.3 m section-1). Likewise, the concentration of Rb in shoots was, on average, 7-fold greater where Rb was applied to the limed (vs. acidic) subsoil section and was positively influenced by the rate of Rb amendment in the limed (p ≤ 0.05), but not the acidic section of the subsoil. Rubidium uptake into shoots was significantly correlated (p ≤ 0.05) with the length of roots within the Rb-amended subsoil section. The uptake of Rb from acidic or limed subsoil sections was determined by the root length in the Rb-amended subsoil section, regardless of the rate of Rb amendment. The uptake of Rb per unit of root length from acidic or limed sections of subsoil was not significantly different. The data validate the use of Rb as a tracer for the dynamics of root length proliferation in limed subsoil sections in a heterogeneously limed acidic soil profile.
RESUMO
Cultivars with increased efficiency of uptake and utilization of soil nutrients are likely to have positive environmental effects through reduced usage of chemicals in agriculture. This review assesses the available literature on differential uptake and utilization efficiency of K in farming systems. Large areas of agricultural land in the world are deficient in K (e.g. 3/4 of paddy soils in China, 2/3 of the wheatbelt in Southern Australia), with export in agricultural produce (especially hay) and leaching (especially in sandy soils) contributing to lowering of K content in the soil. The capacity of a genotype to grow and yield well in soils low in available K is K efficiency. Genotypic differences in efficiency of K uptake and utilization have been reported for all major economically important plants. The K-efficient phenotype is a complex one comprising a mixture of uptake and utilization efficiency mechanisms. Differential exudation of organic compounds to facilitate release of non-exchangeable K is one of the mechanisms of differential K uptake efficiency. Genotypes efficient in K uptake may have a larger surface area of contact between roots and soil and increased uptake at the root-soil interface to maintain a larger diffusive gradient towards roots. Better translocation of K into different organs, greater capacity to maintain cytosolic K(+) concentration within optimal ranges and increased capacity to substitute Na(+) for K(+) are the main mechanisms underlying K utilization efficiency. Further breeding for increased K efficiency will be dependent on identification of suitable markers and compounding of efficiency mechanisms into locally adapted germplasm.
