Temporal and spatial variations of carbon isotope signature reveal substantial contribution of bracts and internode assimilates to grain filling of japonica rice

Carbon isotope composition(δ^(13)C)of a plant organ is an inherent signature reflecting its physiological property,and thus is used as an integrative index in crop breeding.It is also a non-intrusive method for quantifying the relative contribution of different source organs to grain filling in cereals.Using the samples collected from two-year field and pot experiments with two nitrogen(N)fertilization treatments,we investigated the temporal and spatial variations of δ^(13)C in source organs of leaf,sheath,internode,and bracts,and in sink organ grain.Constitutive nature of δ^(13)C was uncovered,with an order of leaf(−27.84‰)<grain(−27.82‰)<sheath(−27.24‰)<bracts(−26.81‰)<internode(−25.67‰).For different positions of individual organs within the plant,δ^(13)C of the leaf and sheath presented a diminishing trend from the top(flag leaf and its sheath)to the bottom(the last leaf in reverse order and its sheath).No obvious pattern was found for the internode.For temporal variations, δ^(13)C of the leaf and sheath had a peak(the most negative)at 10 days after anthesis(DAA),whereas that of the bracts showed a marked increase at the time point of anthesis,implying a transformation from sink to source organ.By comparing the δ^(13)C in its natural abundance in the water-soluble fractions of the sheath,internode,and bracts with the δ^(13)C in mature grains,the relative contribution of these organs to grain filling was assessed.With reference to the leaf,the internode accounted for as high as 32.64%and 42.56%at 10 DAA and 20 DAA,respectively.Meanwhile,bracts presented a larger contribution than the internode,with superior bracts being higher than inferior bracts.In addition,N topdressing reduced the contribution of the internode and bracts.Our findings clearly proved the actual significance of non-foliar organs of the internode and bracts for rice yield formation,thus extending our basic knowledge of source and sink relations.

The role of soluble sugars during drought in tropical tree seedlings with contrasting tolerances

Aims Non-structural carbohydrates(NSCs)are plant storage compounds used for metabolism,transport,osmoregulation and regrowth following the loss of plant tissue.Even in conditions suitable for optimal growth,plants continue to store NSCs.This storage may be due to passive accumulation from sink-inhibited growth or active reserves that come at the expense of growth.The former pathway implies that NSCs may be a by-product of sink limitation,while the latter suggests a functional role of NSCs for use during poor conditions.Methods Using 13C pulse labelling,we traced the source of soluble sugars in stem and root organs during drought and everwet conditions for seedlings of two tropical tree species that differ in drought tolerance to estimate the relative allocation of NSCs stored prior to drought versus NSCs assimilated during drought.We monitored growth,stomatal conductance,stem water potential and NSC storage to assess a broad carbon response to drought.Important Findings We found that the drought-sensitive species had reduced growth,conserved NSC concentrations in leaf,stem and root organs and had a larger proportion of soluble sugars in stem and root organs that originated from pre-drought storage relative to seedlings in control conditions.In contrast,the drought-tolerant species maintained growth and stem and root NSC concentrations but had reduced leaf NSCs concentrations with a larger proportion of stem and root soluble sugars originated from freshly assimilated photosynthates relative to control seedlings.These results suggest the drought-sensitive species passively accumulated NSCs during water deficit due to growth inhibition,while the drought-tolerant species actively responded to water deficit by allocating NSCs to stem and root organs.These strategies seem correlated with baseline maximum growth rates,which supports previous research suggesting a trade-off between growth and drought tolerance while providing new evidence for the importance of plasticity in NSC allocation during drought.