1Members of the Centre for Terrestrial Carbon Dynamics (CTCD), a centre of excellence of the Natural Environment Research Council (NERC), UK.
Forest soil CO2 flux: uncovering the contribution and environmental responses of ectomycorrhizas
Article first published online: 19 MAY 2007
Global Change Biology
Volume 13, Issue 8, pages 1786–1797, August 2007
How to Cite
HEINEMEYER, A., HARTLEY, I. P., EVANS, S. P., CARREIRA DE LA FUENTE, J. A. and INESON, P. (2007), Forest soil CO2 flux: uncovering the contribution and environmental responses of ectomycorrhizas. Global Change Biology, 13: 1786–1797. doi: 10.1111/j.1365-2486.2007.01383.x
- Issue published online: 19 MAY 2007
- Article first published online: 19 MAY 2007
- Received 24 August 2006; revised version received 3 January 2007 and accepted 13 March 2007
- lodgepole pine;
- mesh collar;
- mycorrhizal respiration;
- root respiration;
- soil moisture;
- soil respiration;
- substrate supply;
Forests play a critical role in the global carbon cycle, being considered an important and continuing carbon sink. However, the response of carbon sequestration in forests to global climate change remains a major uncertainty, with a particularly poor understanding of the origins and environmental responses of soil CO2 efflux. For example, despite their large biomass, the contribution of ectomycorrhizal (EM) fungi to forest soil CO2 efflux and responses to changes in environmental drivers has, to date, not been quantified in the field. Their activity is often simplistically included in the ‘autotrophic’ root respiration term. We set up a multiplexed continuous soil respiration measurement system in a young Lodgepole pine forest, using a mycorrhizal mesh collar design, to monitor the three main soil CO2 efflux components: root, extraradical mycorrhizal hyphal, and soil heterotrophic respiration.
Mycorrhizal hyphal respiration increased during the first month after collar insertion and thereafter remained remarkably stable. During autumn the soil CO2 flux components could be divided into ∼60% soil heterotrophic, ∼25% EM hyphal, and ∼15% root fluxes. Thus the extraradical EM mycelium can contribute substantially more to soil CO2 flux than do roots. While EM hyphal respiration responded strongly to reductions in soil moisture and appeared to be highly dependent on assimilate supply, it did not responded directly to changes in soil temperature. It was mainly the soil heterotrophic flux component that caused the commonly observed exponential relationship with temperature. Our results strongly suggest that accurate modelling of soil respiration, particularly in forest ecosystems, needs to explicitly consider the mycorrhizal mycelium and its dynamic response to specific environmental factors. Moreover, we propose that in forest ecosystems the mycorrhizal CO2 flux component represents an overflow ‘CO2 tap’ through which surplus plant carbon may be returned directly to the atmosphere, thus limiting expected carbon sequestration from trees under elevated CO2.