Abstract
The dynamics of C partitioning with Lolium perenne and its associated rhizosphere was investigated in plant-soil microcosms using 14C pulse-chase labelling. The 14CO2 pulse was introduced into the shoot chamber and the plants allowed to assimilate the label for a fixed period. The microcosm design facilitated independent monitoring of shoot and root/soil respiration during the chase period. Partitioning between above- and below-ground pools was determined between 30 min and 168 h after the pulse, and the distribution was found to vary with the length of the chase period. Initially (30 min after the pulse), the 14C was predominantly (99%) in the shoot biomass and declined thereafter. The results indicate that translocation of recent photoassimilate is rapid, with 14C detected below ground within 30 min of pulse application. The translocation rate of 14C below ground was maximal (6.2% h-1) between 30 min and 3 h after the pulse, with greatest incorporation into the microbial biomass detected at 3 h. After 3 h, the microbial biomass 14C pool accounted for 74% of the total 14C rhizosphere pool. By 24 h, approximately 30% of 14C assimilate had been translocated below ground; thereafter 14C translocation was greatly reduced. Partitioning of recent assimilate changed with increasing CO2 concentration. The proportion of 14C translocated below ground almost doubled from 17.76% at the ambient atmospheric CO2 concentration (450 ppm) to 33.73% at 750 ppm CO2 concentration. More specifically, these changes occurred in the root biomass and the total rhizosphere pools, with two- and threefold 14C increases at an elevated CO2 concentration compared to ambient, respectively. The pulselabelling strategy developed in this study provided sufficient sensitivity to determine perturbations in C dynamics in L. perenne, in particular rhizosphere C pools, in response to an elevated atmospheric CO2 concentration.
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