Soil acidification is an ongoing problem in intensively cultivated croplands due to inefficient and excessive nitrogen (N) fertilization. We collected high-resolution data comprising 19,969 topsoil (0–20 cm) samples from the Land Use and Coverage Area frame Survey (LUCAS) of the European commission in 2009 to assess the impact of N fertilization on buffering substances such as carbonates and base cations. We have only considered the impacts of mineral fertilizers from the total added N, and a N use efficiency of 60 %. Nitrogen fertilization adds annually 6.1 × 107 kmol H+ to European croplands, leading to annual loss of 6.1 × 109 kg CaCO3. Assuming similar acidification during the next 50 years, soil carbonates will be completely removed from 3.4 × 106 ha of European croplands. In carbonate-free soils, annual loss of 2.1 × 107 kmol of basic cations will lead to strong acidification of at least 2.6 million ha of European croplands within the next 50 years. Inorganic carbon and basic cation losses at such rapid scale tremendously drop the nutrient status and production potential of croplands. Soil liming to ameliorate acidity increases pH only temporarily and with additional financial and environmental costs. Only the direct loss of soil carbonate stocks and compensation of carbonate-related CO2 correspond to about 1.5 % of the proposed budget of the European commission for 2023. Thus, controlling and decreasing soil acidification is crucial to avoid degradation of agricultural soils, which can be done by adopting best management practices and increasing nutrient use efficiency. Regular screening or monitoring of carbonate and base cations contents, especially for soils, where the carbonate stocks are at critical levels, are urgently necessary.
The rhizosphere is a very important and dynamic hotspot of microbial activity in soil. Consequently, the enzyme activities in the rhizosphere are a footprint of complex plant-microbial interactions and may reflect functional response to climate changes.The temperature sensitivity of enzymes responsible for organic matter decomposition in soil is crucial for predicting the effects of global warming on the carbon cycle and sequestration. For the first time, we applied the in situ soil zymography for identification and localization of hotspots of phosphatase and chitinase activity in the rhizosphere of rice (Oryza sativa L.) under warming effect - (18 and 25 °C) after 14 and 30 days. Thus, we test the hypotheses that due to high inputs of easily degradable organic compounds from the roots canceling effect: strong reduction of temperature sensitvity (Q10~1) of catalytic reactions will not accoure in the rhizosphere. Correspondingly, the Q10 values for reaction rates were always >1, at root-soil interface, with the average range of 1.3 –1.4 Independent of enzymes, canceling was never observed at vicinity of root. Thus, canceling effect is a substrate concentration dependence phenomenon. To our knowledge, this is the first study explored the canceling effect in the rhizosphere. Absence of canceling at root-soil interface for phosphates and chitinase revealed that warming will accelerate P and N mobilization in the rhizosphere. Altogether, for the first time we showed that extent of enzyme activity’s rhizosphere is constant, temporally however, there is a temporal heterogeneity of enzymatic hotspots localization in soil. Thus, increasing in temperature had a positive impact on overall enzyme activities, Rice growth and root development, conducted an enzyme specific impact on hotspots percentage and localization patterns. We conclude that absence of canceling at root-soil interface for tested enzymes revealed that warming will accelerate nutrient mobilization in the rhizosphere more than root free soil.
No abstract is provided for this article.
No abstract is provided for this article.
Soil fertility and (micro)biological activities are prominent indicators of soil ecological functions interrelated with nutrient cycles and stocks. The responses of soil functions and belowground biota to degradation of natural ecosystems and land use changes have received little attention, especially in semi-arid ecosystems of mountainous areas that are sensitive and fragile habitats. Soils were sampled from two natural vegetation types: forest (Carpinus orientalis - Zelkova carpinifolia) and rangeland (Berberis integerrima - Crataegus melanocarpa), and two cultivated croplands (under Triticum aestivum), located in a mountainous semi-arid region of northern Iran, that were converted from the forests and rangelands thirty years ago. Soil properties, C and N stocks and fractions, and related microbial activities were analysed in 0–10 and 10–20 cm. C stocks in the upper 10 cm soil were affected by land use, while no differences were found in the lower depth. C stocks in the topsoil reached 49, 37, 33 and 29 Mg ha−1 for forest, rangeland, croplands (converted from forest and converted from rangeland), respectively. Soil N stocks under forest (5.2 Mg ha−1 for top 10 cm and 4.8 Mg ha−1 for 10–20 cm depths) were higher compared to the other land use types. Particulate and dissolved organic matters under croplands were almost half of that under forest and rangeland. High soil respiration, microbial biomass, ammonium and nitrate content, as well as N mineralization in 0–10 cm under forest were 2 times larger than in 10–20 cm. Concluding, conversion of forest and rangeland to croplands (converted from forest > converted from rangeland) has decreased the functions of soil due to removal of tree cover, decreasing litter layer, organic matter input and soil moisture and also increase of soil temperature. Consequently, more care should be taken by preserving natural vegetation in mountainous semi-arid ecosystems, and higher organic inputs are necessary to maintain microbial properties and functions.
. The frequency of dry-season droughts and wet-season storms has been predicted to increase in subtropical areas in the coming decades. Since subtropical forest soils are significant sources of N2O and NO3−, it is important to understand the features and determinants of N transformation responses to the predicted precipitation changes. A precipitation manipulation field experiment was conducted in a subtropical forest to reduce dry-season precipitation and increase wet-season precipitation, with annual precipitation unchanged. Net N mineralization, net nitrification, N2O emission, nitrifying (bacterial and archaeal amoA) and denitrifying (nirK, nirS and nosZ) gene abundance, microbial biomass carbon (MBC), extractable organic carbon (EOC), NO3−, NH4+ and soil water content (SWC) were monitored to characterize and explain soil N transformation responses. Dry-season precipitation reduction decreased net nitrification and N mineralization rates by 13–20 %, while wet-season precipitation addition increased both rates by 50 %. More than 20 % of the total variation of net nitrification and N mineralization could be explained by microbial abundance and SWC. Notably, archaeal amoA abundance showed the strongest correlation with net N transformation rates (r ≥ 0.35), suggesting the critical role of archaeal amoA abundance in determining N transformations. Increased net nitrification in the wet season, together with large precipitation events, caused substantial NO3− losses via leaching. However, N2O emission decreased moderately in both dry and wet seasons due to changes in nosZ gene abundance, MBC, net nitrification and SWC (decreased by 10–21 %). We conclude that reducing dry-season precipitation and increasing wet-season precipitation affect soil N transformations through altering functional microbial abundance and MBC, which are further affected by changes in EOC and NH4+ availabilities.
Roots release a wide range of organic compounds called rhizodeposits, which affect some of the soil parameters such as pH, water holding capacity, stability of the soil aggregates or microbial activity. They are also considered to be one of the major sources of the carbon (C) for rhizospheric microorganisms and contribute to CO2 emission from soil, making up to 60 % of total CO2 efflux from soil. Additionally, rhizodeposits can alter soil organic matter (SOM) decomposition rates. Because of these strong reasons, therefore, the carbon translocation by plants was investigated. The distribution pattern of tracer (14C) in the system plant-soil by means of the pulse labelling has been investigated in the pot-scale experiment. Rhizosphere-derived CO2 accounted for 11 % of total assimilated 14C. The 14C activity and total carbon presented in the roots, rhizosphere-derived CO2, microbial biomass (MB), dissolved organic carbon (DOC) in the soil have been measured. Maximal 14C activity in DOC and MB occurred at the sixth hour while in the roots it was detected at twelfth hour after labelling. The changes of the 14C content in investigated pools have been divided into two phases: the first phase lasted for first four days after labelling with fast decrease of 14C and in the next phase only inconsiderable changes occurred.
Stability and transformation products of incomplete combustion of vegetation or fossil fuel, frequently called pyrogenic or black carbon and of biochar in soil, remains unknown mainly because of their high recalcitrance compared to other natural substances. Therefore, direct estimations of biochar decomposition and transformations are difficult because 1) changes are too small for any relevant experimental period and 2) due to methodological constraints (ambiguity of the origin of investigated compounds). We used 14C-labeled biochar to trace its decomposition to CO2 during 8.5 years and transformation of its chemical compounds: neutral lipids, glycolipids, phospholipids, polysaccharides and benzenepolycarboxylic acids (BPCA). 14C-labeled biochar was produced by charring 14C-labeled Lolium residues. We incubated the 14C-labeled biochar in a Haplic Luvisol and in loess for 8.5 years under controlled conditions. In total only about 6% of initially added biochar were mineralized to CO2 during the 8.5 years. This is probably the slowest decomposition obtained experimentally for any natural organic compound. The biochar decomposition rates estimated by 14CO2 efflux between the 5th and 8th years were of 7 × 10−4 % per day. This corresponds to less than 0.3% per year under optimal conditions and is about 2.5 times slower as reported from the previous shorter study (3.5 years). After 3.5 years of incubation, we analyzed 14C in dissolved organic matter, microbial biomass, and sequentially extracted neutral lipids, glycolipids, phospholipids, polysaccharides and BPCA. Biochar-derived C (14C) in microbial biomass ranged between 0.3 and 0.95% of the 14C input. Biochar-derived C in all lipid fractions was less than 1%. Over 3.5 years, glycolipids and phospholipids were decomposed 1.6 times faster (23% of their initial content per year) compared to neutral lipids (15% year−1). Polysaccharides contributed ca. 17% of the 14C activity in biochar. The highest portion of 14C in the initial biochar (87%) was in BPCA decreasing only 7% over 3.5 years. Condensed aromatic moieties were the most stable fraction compared to all other biochar compounds and the high portion of BPCA in biochar explains its very high stability and its contribution to long-term C sequestration in soil. Our new approach for analysis of biochar stability combines 14C-labeled biochar with 14C determination in chemical fractions allowed tracing of transformation products not only in released CO2 and in microbial biomass, but also evaluation of decomposition of various biochar compounds with different chemical properties.