Abstract

Variations in the carbon isotope signature of leaf dark-respired CO2 (δ13CR) within a single night is a widely observed phenomenon. However, it is unclear whether there are plant functional type differences with regard to the amplitude of the nighttime variation in δ13CR. These differences, if present, would be important for interpreting the short-term variations in the stable carbon signature of ecosystem respiration and the partitioning of carbon fluxes. To assess the plant functional type differences relating to the magnitude of the nighttime variation in δ13CR and the respiratory apparent fractionation, we measured the δ13CR, the leaf gas exchange, and the δ13C of the respiratory substrates of 22 species present in the agricultural-pastoral zone of the Songnen Plain, northeast China. The species studied were grouped into C3 and C4 plants, trees, grasses, and herbs. A significant nocturnal shift in δ13CR was detected in 20 of the studied species, with the magnitude of the shift ranging from 1‰ to 5.8‰. The magnitude of the nighttime variation in δ13CR was strongly correlated with the daytime cumulative carbon assimilation, which suggests that variation in δ13CR were influenced, to some extent, by changes in the contribution of malate decarboxylation to total respiratory CO2 flux. There were no differences in the magnitude of the nighttime variation in δ13CR between the C3 and C4 plants, as well as among the woody plants, herbs and graminoids. Leaf respired CO2 was enriched in 13C compared to biomass, soluble carbohydrates and lipids; however the magnitude of enrichment differed between 8 pm and 4 am, which were mainly caused by the changes in δ13CR. We also detected the plant functional type differences in respiratory apparent fractionation relative to biomass at 4 am, which suggests that caution should be exercised when using the δ13C of bulk leaf material as a proxy for the δ13C of leaf-respired CO2.

Highlights

  • The stable C isotope composition (δ13C) has been widely used to trace the carbon flow within ecosystem components or between the ecosystem and the atmosphere [1,2,3,4,5,6,7]

  • The magnitude of the nighttime variation in δ13C of leaf-respired CO2 (δ13CR) was strongly correlated with the daytime cumulative carbon assimilation, which suggests that variation in δ13CR were influenced, to some extent, by changes in the contribution of malate decarboxylation to total respiratory CO2 flux

  • There was no significant difference in the mean R among the functional groups, and it did not differ between the C3 and the C4 species either (Table 3)

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Summary

Introduction

The stable C isotope composition (δ13C) has been widely used to trace the carbon flow within ecosystem components or between the ecosystem and the atmosphere [1,2,3,4,5,6,7]. Leaf dark-respired CO2 is often enriched in 13C compared with leaf bulk tissue or other potential respiratory substrates, such as starch, soluble carbohydrates, and others [27,28,29] This phenomenon is attributed mainly to non-homogeneous 13C distribution among the carbon atoms within the hexose molecules and the incomplete oxidation of hexoses. For instance, allocated proportionally more acetyl-CoA to the synthesis of lipids and lignin than did grasses [14, 26] This could lead to the leaf-respired CO2 in trees being more enriched in 13C in comparison with the putative respiratory substrates or the bulk leaf material. The existence of plant functional type differences with regard to respiratory apparent fractionation needs to be further verified and, if they do exist, we need to incorporate these into the flux partitioning

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