Quantification of effects of season and nitrogen supply on tree below-ground carbon transfer to ectomycorrhizal fungi and other soil organisms in a boreal pine forest
- PMID: 20456043
- DOI: 10.1111/j.1469-8137.2010.03274.x
Quantification of effects of season and nitrogen supply on tree below-ground carbon transfer to ectomycorrhizal fungi and other soil organisms in a boreal pine forest
Abstract
*The flux of carbon from tree photosynthesis through roots to ectomycorrhizal (ECM) fungi and other soil organisms is assumed to vary with season and with edaphic factors such as nitrogen availability, but these effects have not been quantified directly in the field. *To address this deficiency, we conducted high temporal-resolution tracing of (13)C from canopy photosynthesis to different groups of soil organisms in a young boreal Pinus sylvestris forest. *There was a 500% higher below-ground allocation of plant C in the late (August) season compared with the early season (June). Labelled C was primarily found in fungal fatty acid biomarkers (and rarely in bacterial biomarkers), and in Collembola, but not in Acari and Enchytraeidae. The production of sporocarps of ECM fungi was totally dependent on allocation of recent photosynthate in the late season. There was no short-term (2 wk) effect of additions of N to the soil, but after 1 yr, there was a 60% reduction of below-ground C allocation to soil biota. *Thus, organisms in forest soils, and their roles in ecosystem functions, appear highly sensitive to plant physiological responses to two major aspects of global change: changes in seasonal weather patterns and N eutrophication.
Similar articles
-
High temporal resolution tracing of photosynthate carbon from the tree canopy to forest soil microorganisms.New Phytol. 2008;177(1):220-228. doi: 10.1111/j.1469-8137.2007.02238.x. Epub 2007 Oct 18. New Phytol. 2008. PMID: 17944822
-
Greater carbon allocation to mycorrhizal fungi reduces tree nitrogen uptake in a boreal forest.Ecology. 2016 Apr;97(4):1012-22. doi: 10.1890/15-1222.1. Ecology. 2016. PMID: 27220217
-
Are ectomycorrhizal fungi alleviating or aggravating nitrogen limitation of tree growth in boreal forests?New Phytol. 2013 Apr;198(1):214-221. doi: 10.1111/nph.12139. Epub 2013 Jan 29. New Phytol. 2013. PMID: 23356503
-
Atmospheric nitrogen deposition impacts on the structure and function of forest mycorrhizal communities: A review.Environ Pollut. 2019 Mar;246:148-162. doi: 10.1016/j.envpol.2018.11.074. Epub 2018 Nov 28. Environ Pollut. 2019. PMID: 30543941 Review.
-
The mycorrhizal-associated nutrient economy: a new framework for predicting carbon-nutrient couplings in temperate forests.New Phytol. 2013 Jul;199(1):41-51. doi: 10.1111/nph.12221. Epub 2013 Apr 17. New Phytol. 2013. PMID: 23713553 Review.
Cited by
-
Close coupling of plant functional types with soil microbial community composition drives soil carbon and nutrient cycling in tundra heath.Plant Soil. 2023;488(1-2):551-572. doi: 10.1007/s11104-023-05993-w. Epub 2023 Mar 27. Plant Soil. 2023. PMID: 37600962 Free PMC article.
-
Effects of nitrogen addition and root fungal inoculation on the seedling growth and rhizosphere soil microbial community of Pinus tabulaeformis.Front Microbiol. 2022 Oct 19;13:1013023. doi: 10.3389/fmicb.2022.1013023. eCollection 2022. Front Microbiol. 2022. PMID: 36338078 Free PMC article.
-
The responses to long-term nitrogen addition of soil bacterial, fungal, and archaeal communities in a desert ecosystem.Front Microbiol. 2022 Oct 13;13:1015588. doi: 10.3389/fmicb.2022.1015588. eCollection 2022. Front Microbiol. 2022. PMID: 36312972 Free PMC article.
-
Photosynthetic product allocations of Pinus massoniana seedlings inoculated with ectomycorrhizal fungi along a nitrogen addition gradient.Front Plant Sci. 2022 Aug 12;13:948676. doi: 10.3389/fpls.2022.948676. eCollection 2022. Front Plant Sci. 2022. PMID: 36035728 Free PMC article.
-
Overfertilization reduces tomato yield under long-term continuous cropping system via regulation of soil microbial community composition.Front Microbiol. 2022 Aug 4;13:952021. doi: 10.3389/fmicb.2022.952021. eCollection 2022. Front Microbiol. 2022. PMID: 35992643 Free PMC article.
References
-
- Aber J, McDowell W, Nadelhoffer K, Magill A, Berntson G, Kamakea M, McNulty S, Currie W, Rustad L, Fernandez I. 1998. Nitrogen saturation in temperate forest ecosystems - hypotheses revisited. Bioscience 48: 921-934.
-
- Bahn M, Schmitt M, Siegwolf R, Richter A, Brüggemann N. 2009. Does photosynthesis affect grassland soil-respired CO2 and its carbon isotope composition on a diurnal timescale? New Phytologist 182: 451-460.
-
- Berg B, McClaugherty C. 2003. Plant litter decomposition, humus formation, carbon sequestration. Berlin, Germany: Springer.
-
- Carbone MS, Czimczik CI, McDuffee KE, Trumbore SE. 2007. Allocation and residence times of photosynthetic products in a boreal forest using a low-level 14C pulse-chase labelling technique. Global Change Biology 13: 466-477.
-
- Dise NB, Wright RF. 1995. Nitrogen leaching from European forests in relation to nitrogen deposition. Forest Ecology and Management 71: 153-162.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
