scholarly journals A soil microbial model to analyze decoupled microbial growth and respiration during soil drying and rewetting

2020 ◽  
Vol 148 ◽  
pp. 107871
Author(s):  
Albert C. Brangarí ◽  
Stefano Manzoni ◽  
Johannes Rousk
2021 ◽  
Author(s):  
Blandine Lyonnard ◽  
Albert Brangarí ◽  
Johannes Rousk

<p>The alternation of drought periods and rainfall events, intensified by climate change, has huge impacts on carbon cycle dynamics. Changes in soil moisture induce significant releases of CO<sub>2</sub> from soils to the atmosphere. This phenomenon, known as the Birch effect, is accompanied by drastic changes in the microbiology as well. Based on the response patterns of microbial growth and respiration to the rewetting of dry soil, two different types have been identified. Microbial communities either respond immediately after rewetting and start increasing growth in a linear way (so-called “type 1” response), or they recover growth after a lag phase preceding an exponential increase (“type 2” response). The reasons behind the different responses, including how harsh the drought is perceived by the communities and what history of moisture conditions they were subjected to, are not yet fully resolved. Moreover, most studies focus on the top few centimeters of soil and the effect of depth and the contribution of deeper soils to the overall dynamics have been largely overlooked.</p><p>In order to investigate the influence of depth on microbial dynamics during drought and rainfall events, taking into account land-use, we performed a set of laboratory experiments that were also used to parameterize and validate numerical modelling-based analysis of the ecology driving soil biogeochemistry. We collected soil samples from permanent pasture and tilled and cropped arable fields at two different depths (0-5 cm and 20-30 cm). We then subjected them to a week of air drying followed by rewetting to optimal moisture, and measured respiration, bacterial growth and fungal growth at high temporal resolution.</p><p>The patterns were significantly different between soil types, showing type 1 responses in arable soils and type 2 responses in pasture soils. The type 1 responses in arable soils were also characterized by a higher carbon use efficiency after the rewetting perturbation. Moreover, the deeper microbial communities were relatively more affected by the drying and rewetting experiment than the respective shallow ones. Taken together, these results suggested that the drying and rewetting event was perceived by soil microbial communities as a stronger disturbance in the pasture soils, and at deeper depths, as illustrated by more sensitive microbial responses.</p><p>We then incorporated these laboratory data into a soil microbial model (EcoSMMARTS) and identified the depth- and community-specific differences in osmolyte regulation, necromass turnover, and cell residue activity as the microbial mechanisms potentially explaining the observed patterns. These findings provide insights into soil-climate feedback from different ecosystems, where intensively used arable soils were more resilient than permanent pasture soils and stored larger amounts of carbon due to a higher fraction of microbial growth to respiration under climate change scenarios. The capacity of microbial communities to adapt and regulate soil carbon dynamics is not uniform through the soil profile nor across management practices, therefore indicating a need for future studies incorporating depth and especially land-use which has the strongest effect on microbial activity during soil drying and rewetting.</p>


2015 ◽  
Vol 12 (14) ◽  
pp. 11191-11216 ◽  
Author(s):  
Z. H. Zhou ◽  
C. K. Wang

Abstract. Microbial metabolism plays a key role in regulating the biogeochemical cycle of forest ecosystems, but the mechanisms driving microbial growth are not well understood. Here, we synthesized 689 measurements on soil microbial biomass carbon (Cmic) and nitrogen (Nmic) and related parameters from 207 independent studies published during the past 15 years across China's forest ecosystems. Our objectives were to (1) examine patterns in Cmic, Nmic, and microbial quotient (i.e., Cmic / Csoil and Nmic / Nsoil rates) by climate zones and management regimes for these forests; and (2) identify the factors driving the variability in the Cmic, Nmic, and microbial quotient. There was a large variability in Cmic (390.2 mg kg−1), Nmic (60.1 mg kg−1), Cmic : Nmic ratio (8.25), Cmic / Csoil rate (1.92 %), and Nmic / Nsoil rate (3.43 %) across China's forests, with coefficients of variation varying from 61.2 to 95.6 %. The natural forests had significantly greater Cmic and Nmic than the planted forests, but had less Cmic : Nmic ratio and Cmic / Csoil rate. Soil resources and climate together explained 24.4–40.7 % of these variations. The Cmic : Nmic ratio declined slightly with the Csoil : Nsoil ratio, and changed with latitude, mean annual temperature and precipitation, suggesting a plastic homeostasis of microbial carbon-nitrogen stoichiometry. The Cmic / Csoil and Nmic / Nsoil rates were responsive to soil resources and climate differently, suggesting that soil microbial assimilation of carbon and nitrogen be regulated by different mechanisms. We conclude that soil resources and climate jointly drive microbial growth and metabolism, and also emphasize the necessity of appropriate procedures for data compilation and standardization in cross-study syntheses.


1982 ◽  
Vol 62 (1) ◽  
pp. 125-137 ◽  
Author(s):  
C. A. CAMPBELL ◽  
V. O. BIEDERBECK

The aim of this study was to identify, in situ, some of the microbial responses to environmental conditions previously noted in experiments in the laboratory and field. Soil samples were taken from a Brown Chernozem under a wheat-fallow rotation at 2-wk intervals during spring and autumn and at 4-wk intervals in winter and summer for a 2-yr period. Nitrate-N and exchangeable NH4-N, and numbers of bacteria and actinomycetes by plate count, were measured in 0- to 2.5-cm, 2.5- to 15-cm and 15- to 30-cm soil layers. Changes in microbial numbers and mineral N were correlated with soil depth, available carbon and environmental conditions. Bacterial numbers ranged between 14 and 119 million per gram of soil in the 0- to 2.5-cm layer, between 9 and 47 million in the 2.5-to 15-cm layer and were 4 million in the 15- to 30-cm soil layer. Bacteria:actinomycetes ratios were 3:1 in the 0- to 2.5-cm layer, 2:1 in the 2.5- to 15-cm layer and 1:1 in the 15- to 30-cm layer. Exchangeable NH4- and NO3-N as high as 20 and 280 ppm, respectively, were found in the top 2.5 cm. Different processes with similar or opposing effects often occurred simultaneously, thus making interpretation difficult. However, we identified (i) the stepwise nature of the ammonification-nitrification process; (ii) the importance of crop residues in microbial growth, and denitrification; (iii) the flush in microbial growth when a dry soil is moistened; (iv) the importance of the tilled layer as the prime site of soil microbial activity; and (v) the rapid decrease in microbial population and activity below the tilled soil layer. There was also evidence of possible upward movement of NO3 due to temperature gradient (as soil froze), and due to evaporation.


2020 ◽  
Author(s):  
Jie Zhou ◽  
Yuan Wen ◽  
Lingling Shi ◽  
Michaela Dippold ◽  
Yakov Kuzyakov ◽  
...  

<p>The Paris climate agreement is pursuing efforts to limit the increase in global temperature to below 2 °C above pre-industrial level. The overall consequence of relatively slight warming (~2 °C), on soil C and N stocks will be dependent on microorganisms decomposing organic matter through release of extracellular enzymes. Therefore, the capacity of soil microbial community to buffer climate warming in long-term and the self-regulatory mechanisms mediating soil C and N cycling through enzyme activity and microbial growth require a detailed comparative study. Here, microbial growth and the dynamics of enzyme activity (involved in C and N cycling) in response to 8 years warming (ambient, +1.6 °C, +3.2 °C) were investigated to identify shifts in soil and microbial functioning. A slight temperature increase (+1.6 °C) only altered microbial properties, but had no effect on either hydrolytic enzyme activity or basic soil properties. Stronger warming (+3.2 °C) increased the specific growth rate (μ<sub>m</sub>) of the microbial community, indicating an alteration in their ecological strategy, i.e. a shift towards fast-growing microorganisms and accelerated microbial turnover. Warming strongly changed microbial physiological state, as indicated by a 1.4-fold increase in the fraction of growing microorganisms (GMB) and 2 times decrease in lag-time with warming. This reduced total microbial biomass but increased specific enzyme activity to be ready to decompose increased rhizodeposition, as supported by the higher potential activitiy (V<sub>max</sub>) and lower affinity to substrates (higher K<sub>m</sub>) of enzymes hydrolyzing cellobiose and proteins cleavage in warmed soil. In other words, stronger warming magnitude (+3.2 °C) changed microbial communities, and was sufficient to benefit fast-growing microbial populations with enzyme functions that specific to degrade labile SOM. Combining with 48 literature observations, we confirmed that the slight magnitude of temperature increase (< 2 °C) only altered microbial properties, but further temperature increases (2-4 °C) was sufficient to change almost all soil, microbial, and enzyme properties and related processes. As a consequence, the revealed microbial regulatory mechanism of stability of soil C storage is strongly depended on the magnitude of future climate warming.</p>


1979 ◽  
Vol 11 (3) ◽  
pp. 317-319 ◽  
Author(s):  
G.P. Sparling ◽  
M.V. Cheshire

2017 ◽  
Vol 220 ◽  
pp. 504-513 ◽  
Author(s):  
A.D. Samarajeewa ◽  
J.R. Velicogna ◽  
J.I. Princz ◽  
R.M. Subasinghe ◽  
R.P. Scroggins ◽  
...  

Elem Sci Anth ◽  
2020 ◽  
Vol 8 (1) ◽  
Author(s):  
Grace Pold ◽  
Luiz A. Domeignoz-Horta ◽  
Kristen M. DeAngelis

Soils store more carbon than the biosphere and atmosphere combined, and the efficiency to which soil microorganisms allocate carbon to growth rather than respiration is increasingly considered a proxy for the soil capacity to store carbon. This carbon use efficiency (CUE) is measured via different methods, and more recently, the 18O-H2O method has been embraced as a significant improvement for measuring CUE of soil microbial communities. Based on extrapolating 18O incorporation into DNA to new biomass, this measurement makes various implicit assumptions about the microbial community at hand. Here we conducted a literature review to evaluate how viable these assumptions are and then developed a mathematical model to test how violating them affects estimates of the growth component of CUE in soil. We applied this model to previously collected data from two kinds of soil microbial communities. By changing one parameter at a time, we confirmed our previous observation that CUE was reduced by fungal removal. Our results also show that depending on the microbial community composition, there can be substantial discrepancies between estimated and true microbial growth. Of the numerous implicit assumptions that might be violated, not accounting for the contribution of sources of oxygen other than extracellular water to DNA leads to a consistent underestimation of CUE. We present a framework that allows researchers to evaluate how their experimental conditions may influence their 18O-H2O-based CUE measurements and suggest the parameters that need further constraining to more accurately quantify growth and CUE.


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