Abstract
The below-ground growing season often extends beyond the above-ground growing season in tundra ecosystems and as the climate warms, shifts in growing seasons are expected. However, we do not yet know to what extent, when and where asynchrony in above- and below-ground phenology occurs and whether variation is driven by local vegetation communities or spatial variation in microclimate. Here, we combined above- and below-ground plant phenology metrics to compare the relative timings and magnitudes of leaf and fine-root growth and senescence across microclimates and plant communities at five sites across the Arctic and alpine tundra biome. We observed asynchronous growth between above- and below-ground plant tissue, with the below-ground season extending up to 74% (~56 days) beyond the onset of above-ground leaf senescence. Plant community type, rather than microclimate, was a key factor controlling the timing, productivity, and growth rates of fine roots, with graminoid roots exhibiting a distinct ‘pulse’ of growth later into the growing season than shrub roots. Our findings indicate the potential of vegetation change to influence below-ground carbon storage as the climate warms and roots remain active in unfrozen soils for longer. Taken together, our findings of increased root growth in soils that remain thawed later into the growing season, in combination with ongoing tundra vegetation change including increased shrub and graminoid abundance, indicate increased below-ground productivity and altered carbon cycling in the tundra biome.
| Original language | English |
|---|---|
| Article number | e70153 |
| Journal | Global Change Biology |
| Volume | 31 |
| Issue number | 4 |
| DOIs | |
| State | Published - Apr 2025 |
Funding
Funding: The research was funded by an E4 PhD scholarship and Envision Doctoral Training Partnership funded by the Natural Environment Research Council, the Tundra Time Project funded by the Natural Environment Research Council, the 2021 Davis Expedition fund, the Niwot Ridge LTER program and Polar Programs funded by the US National Science Foundation, the NGEE Arctic project funded by the Biological and Environmental Research program in the US Department of Energy’s Office of Science, the University of British Columbia Biodiversity Research Centre Postdoctoral Fellowship, and the Norwegian Research Council. The research was funded by an E4 PhD scholarship funded by the Natural Environment Research Council (NERC, NE/S007407/1) and the 2021 Davis Expedition fund acquired by EG and NERC Tundra Time Project (NE/W006448/1) acquired by IMS. S.E. was supported by the US National Science Foundation-supported Niwot Ridge LTER program (NSF DEB 1627686 and NSF DEB 2224439) and Polar Programs (NSF OPP 1836839). C.M.I. and V.G.S. were supported by the NGEE Arctic project, funded by the Biological and Environmental Research program in the US Department of Energy's Office of Science. C.G.C. was supported by a University of British Columbia Biodiversity Research Centre Postdoctoral Fellowship. IA was supported by Norwegian Research Council grant number 294948. L.T. was supported by the Envision Doctoral Training Partnership funded by the Natural Environment Research Council (NE/S007423/1). We thank C. Andrews at the UK Centre for Ecology and Hydrology for access to the Cairngorms ECN Interact site. We thank the Kluane, Champagne, Aishihik, Inuvialuit, Nunamiut, Gwich'in, Koyukuk, Iñupiaq, Ute, Arapaho, Cheyenne and St'àt'imc First Nations for the opportunity to conduct research on their land. We thank the Qikiqtaruk Territorial Park staff as well as the Yukon government, Aurora Research Institute and Yukon Parks for their permission and support of this research. Field assistance was provided by J. Boyle, Z. Leslie, C. Suprenant, E. Zaja, J. Subrt, D. Jerome, J. Everest, C. Hoad, E. Cloutier, and J.G. Smith. Laboratory assistance was provided by M. Hens, J. Subrt, A. Shulmann, E. Bestington, L. Dickenmann, and E. Radeloff. We thank the Editor and three anonymous reviewers for comments that greatly improved our manuscript. The research was funded by an E4 PhD scholarship funded by the Natural Environment Research Council (NERC, NE/S007407/1) and the 2021 Davis Expedition fund acquired by EG and NERC Tundra Time Project (NE/W006448/1) acquired by IMS. S.E. was supported by the US National Science Foundation‐supported Niwot Ridge LTER program (NSF DEB 1627686 and NSF DEB 2224439) and Polar Programs (NSF OPP 1836839). C.M.I. and V.G.S. were supported by the NGEE Arctic project, funded by the Biological and Environmental Research program in the US Department of Energy's Office of Science. C.G.C. was supported by a University of British Columbia Biodiversity Research Centre Postdoctoral Fellowship. IA was supported by Norwegian Research Council grant number 294948. L.T. was supported by the Envision Doctoral Training Partnership funded by the Natural Environment Research Council (NE/S007423/1). We thank C. Andrews at the UK Centre for Ecology and Hydrology for access to the Cairngorms ECN Interact site. We thank the Kluane, Champagne, Aishihik, Inuvialuit, Nunamiut, Gwich'in, Koyukuk, Iñupiaq, Ute, Arapaho, Cheyenne and St'àt'imc First Nations for the opportunity to conduct research on their land. We thank the Qikiqtaruk Territorial Park staff as well as the Yukon government, Aurora Research Institute and Yukon Parks for their permission and support of this research. Field assistance was provided by J. Boyle, Z. Leslie, C. Suprenant, E. Zaja, J. Subrt, D. Jerome, J. Everest, C. Hoad, E. Cloutier, and J.G. Smith. Laboratory assistance was provided by M. Hens, J. Subrt, A. Shulmann, E. Bestington, L. Dickenmann, and E. Radeloff. We thank the Editor and three anonymous reviewers for comments that greatly improved our manuscript.
Keywords
- below-ground
- carbon cycling
- climate change
- permafrost thaw
- phenology
- root dynamics
- root phenology
- tundra ecology
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