(4) University of Amsterdam, Institute of Biodiversity and Ecosystem Dynamics, Earth Surface Science, Amsterdam, Netherlands (k.kalbitz@uva.nl), (1) All-Russian Research Institute of Agricultural Chemistry, Moscow, Russia, (2) University of Hohenheim, Institute of Soil Science and Land Evaluation, Stuttgart, Germany (Sabine.Fiedler@uni-hohenheim.de, (3) University of Bayreuth, Bayreuth Center of Ecology and Environmental Research, Agroecosystem Research, Bayreuth, Germany (kuzyakov@uni-bayreuth.de)
Two recent reviews raised a fundamental question: what is the time lag between photosynthetic C uptake and CO2 efflux from soil. Both reviews, however, in describing the linkages between CO2 assimilation and CO2 efflux from soil, were unable to evaluate the significance of two mechanisms i) the direct transport of assimilates to the roots and rhizosphere and ii) phloem pressure concentration waves. This uncertainty led to a further discussion about the suitability of labeling when evaluating time lags. Here, we estimated the importance of the direct transport of assimilates to the rhizosphere and the importance of phloem pressure concentration waves by various approaches, and reveal further differences between both reviews. We show that the pressure concentration waves only briefly play a role for CO2 efflux. In contrast, the direct transport influence lasts longer and so, it is more important for rhizosphere processes and for CO2 efflux. To evaluate the significance of these two mechanisms, we suggested a new approach based on regressions between the time lag and tree height, which confirms significance of pressure concentration waves only for trees, smaller than 2.5 m.
Nutrient deficiency in most terrestrial ecosystems constrains global primary productivity. Rhizosphere nutrient availability directly regulates plant growth and is influenced by many factors, including soil properties, plant characteristics and climate. A quantitatively comprehensive understanding of the role of these factors in modulating rhizosphere nutrient availability remains largely unknown. We reviewed 123 studies to assess nutrient availability in the rhizosphere compared to bulk soil depending on various factors. The increase in microbial nitrogen (N) content and N-cycling related enzyme activities in the rhizosphere led to a 10% increase in available N relative to bulk soil. The available phosphorus (P) in the rhizosphere decreased by 12% with a corresponding increase in phosphatase activities, indicating extreme demand and competition between plants and microorganisms for P. Greater organic carbon (C) content around taproots (+17%) confirmed their stronger ability to store more organic compounds than the fibrous roots. This corresponds to higher bacterial and fungal contents and slightly higher available nutrients in the rhizosphere of taproots. The maximal rhizosphere nutrient accumulation was common for low-fertile soils, which is confirmed by the negative correlation between most soil chemical properties and the effect sizes of available nutrients. Increases in rhizosphere bacterial and fungal population densities (205–254%) were much higher than microbial biomass increases (indicated as microbial C: +19%). Consequently, despite the higher microbial population densities in the rhizosphere, the biomass of individual microbial cells decreased, pointing on their younger age and faster turnover. This meta-analysis shows that, contrary to the common view, most nutrients are more available in the rhizosphere than in bulk soil because of higher microbial activities around roots.
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Land use change can affect terrestrial C stocks, resulting in increased CO2 flux from soil to the atmosphere. In Africa, conversion of natural ecosystems to agricultural lands is the most common land use change. This study investigated the effects of six land use types occurring in Mt. Kilimanjaro ecosystems i.e. (1) lower montane forest (2) grassland and (3) savannah (natural ecosystems) (4) Chagga homegardens (semi-natural ecosystem) and (5) maize fields and (6) coffee plantation (agroecosystems) on microbial biomass carbon (MBC) and dynamics of 14C labelled glucose added into soil. Decomposition of 14C labelled glucose and its incorporation into microbial biomass in surface soils (0–10 and 10–20 cm) were determined. MBC decreased significantly with increased intensity of land use. Mineralization of the 14C labelled glucose occurred in two phases with contrasting rates: 0–10 days (6–18% of 14C d−1) and 15–65 days (<0.1% of 14C d−1). Land use intensification in agroecosystems led to an average increase of glucose decomposition of 14%. The decay rates of the labile C pool in intensively used agricultural lands were up to three times higher compared to natural ecosystems. The incorporation of 14C glucose into microorganisms ranged between 1 and 7% of 14C input in all soils, and was highest in savannah. Agricultural intensification decreased C content in soil through increased mineralization of organic substances and negatively impacted the upper soil layer more compared to the lower one. Based on these results we conclude that semi-natural ecosystems (e.g. Chagga homegardens) are more sustainable in Mt. Kilimanjaro ecosystems compared to intensive agroecosystems.
Nitrogen (N) fertilization is an indispensable agricultural practice worldwide, serving the survival of half of the global population. Nitrogen transformation (e.g., nitrification) in soil as well as plant N uptake releases protons and increases soil acidification. Neutralizing this acidity in carbonate‐containing soils (7.49 × 10 9 ha; ca. 54% of the global land surface area) leads to a CO 2 release corresponding to 0.21 kg C per kg of applied N. We here for the first time raise this problem of acidification of carbonate‐containing soils and assess the global CO 2 release from pedogenic and geogenic carbonates in the upper 1 m soil depth. Based on a global N‐fertilization map and the distribution of soils containing CaCO 3 , we calculated the CO 2 amount released annually from the acidification of such soils to be 7.48 × 10 12 g C/year. This level of continuous CO 2 release will remain constant at least until soils are fertilized by N. Moreover, we estimated that about 273 × 10 12 g CO 2 ‐C are released annually in the same process of CaCO 3 neutralization but involving liming of acid soils. These two CO 2 sources correspond to 3% of global CO 2 emissions by fossil fuel combustion or 30% of CO 2 by land‐use changes. Importantly, the duration of CO 2 release after land‐use changes usually lasts only 1–3 decades before a new C equilibrium is reached in soil. In contrast, the CO 2 released by CaCO 3 acidification cannot reach equilibrium, as long as N fertilizer is applied until it becomes completely neutralized. As the CaCO 3 amounts in soils, if present, are nearly unlimited, their complete dissolution and CO 2 release will take centuries or even millennia. This emphasizes the necessity of preventing soil acidification in N‐fertilized soils as an effective strategy to inhibit millennia of CO 2 efflux to the atmosphere. Hence, N fertilization should be strictly calculated based on plant‐demand, and overfertilization should be avoided not only because N is a source of local and regional eutrophication, but also because of the continuous CO 2 release by global acidification.