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Titel Transport of root-derived CO2 via the transpiration stream affects aboveground tree physiology
VerfasserIn J. Bloemen, M. A. McGuire, D. P. Aubrey, R. O. Teskey, K. Steppe
Konferenz EGU General Assembly 2012
Medientyp Artikel
Sprache Englisch
Digitales Dokument PDF
Erschienen In: GRA - Volume 14 (2012)
Datensatznummer 250062318
 
Zusammenfassung
Recent research on soil CO2 efflux has shown that belowground autotrophic respiration is largely underestimated using classical net CO2 flux measurements. Aubrey & Teskey (2009) found that in forest ecosystems a substantial portion of the CO2 released from root respiration remained within the root system and was transported aboveground in the stem via the transpiration stream. The magnitude of this upward movement of CO2 from belowground tissues suggested important implications for how we measure above- and belowground respiration. If a considerable fraction of root-respired CO2 is transported aboveground, where it might be fixed in woody and leaf tissues, then we are routinely underestimating the amount of C needed to sustain belowground tissues. In this study, we infused 13C labeled water into the base of field-grown poplar trees as a surrogate for root-respired CO2 to investigate the possible role of root-derived CO2 as substrate for carbon fixation. The label was transported upwards from the base of the tree toward the top. During its ascent, the 13C label was removed from the transpiration stream and fixed by chlorophyll-containing woody (young bark and xylem) and leaf (petiole) tissues. Moreover, based on 13C analysis of gas samples, we observed that up to 88 ±Â 0.10 % of the label applied was lost to the atmosphere by stem and branch efflux higher in the trees. Given that one-half of root-respired CO2 may follow this internal flux pathway (Aubrey & Teskey, 2009), we calculated that up to 44% of the root-respired CO2 could diffuse to the atmosphere once transported to the stem and branches. Thus, a large portion of CO2 that diffuses out of aboveground tissues may actually result from root respiration. Our results show that CO2 originating belowground can be transported internally to aboveground parts of trees, where it will have an important impact on tree physiology. Internal transport of CO2 indicates that the gas exchange approach to estimating above- and belowground autotrophic respiration is inadequate. Accurate quantification of this internal carbon flux is necessary to understand plant physiological mechanisms and to explain variations in above-and belowground respiratory patterns, but these results do not imply the necessity for a reevaluation of net CO2 flux at the ecosystem level. Reference: Aubrey DP, Teskey RO (2009) Root-derived CO2 efflux via xylem stream rivals soil CO2 efflux. New Phytologist 184: 35-40.