scholarly journals Soil aggregate breakdown and carbon release along a chronosequence of recovering landslide scars in a subtropical watershed

CATENA ◽  
2018 ◽  
Vol 165 ◽  
pp. 530-536 ◽  
Author(s):  
J. Schomakers ◽  
H. Mayer ◽  
J.Y. Lee ◽  
T.Y. Lee ◽  
S.H. Jien ◽  
...  
CATENA ◽  
2018 ◽  
Vol 162 ◽  
pp. 354-359 ◽  
Author(s):  
Guanglu Li ◽  
Yu Fu ◽  
Baiqiao Li ◽  
Tenghui Zheng ◽  
Faqi Wu ◽  
...  

2015 ◽  
Vol 29 (4) ◽  
pp. 501-508 ◽  
Author(s):  
Jasmin Schomakers ◽  
Franz Zehetner ◽  
Axel Mentler ◽  
Franz Ottner ◽  
Herwig Mayer

Abstract It has been increasingly recognized that soil organic matter stabilization is strongly controlled by physical binding within soil aggregates. It is therefore essential to measure soil aggregate stability reliably over a wide range of disruptive energies and different aggregate sizes. To this end, we tested highaccuracy ultrasonic dispersion in combination with subsequent sedimentation and X-ray attenuation. Three arable topsoils (notillage) from Central Europe were subjected to ultrasound at four different specific energy levels: 0.5, 6.7, 100 and 500 J cm-3, and the resulting suspensions were analyzed for aggregate size distribution by wet sieving (2 000-63 μm) and sedimentation/X-ray attenuation (63-2 μm). The combination of wet sieving and sedimentation technique allowed for a continuous analysis, at high resolution, of soil aggregate breakdown dynamics after defined energy inputs. Our results show that aggregate size distribution strongly varied with sonication energy input and soil type. The strongest effects were observed in the range of low specific energies (< 10 J cm-3), which previous studies have largely neglected. This shows that low ultrasonic energies are required to capture the full range of aggregate stability and release of soil organic matter upon aggregate breakdown.


2018 ◽  
Author(s):  
Xiaolong Liang ◽  
Mark Radosevich ◽  
Frank Löffler ◽  
Sean M. Schaeffer ◽  
Jie Zhuang

AbstractIn situbioremediation to achieve immobilization of toxic metals and radionuclides or detoxification of chlorinated solvents relies on electron donor additions. This practice promotes microbial Fe(III)-oxide mineral reduction that could change soil pore structure, release soil colloids, alter matrix surface properties, and cause the formation of secondary (i.e., reduced) Fe-mineral phases. These processes in turn may impact rates of bioremediation, groundwater quality, and ultimately contaminant fate. Continuous flow columns packed with water-stable soil aggregates high in Fe-oxides were infused with artificial groundwater containing acetate as electron donor and operated for 20 or 60 days inside an anoxic chamber. Soluble Fe(II) and soil colloids were detected in the effluent within one week after initiation of the acetate addition, demonstrating Fe(III)-bioreduction and colloid formation. Br-, 2,6-difluorobenzoate (DFBA), and silica-shelled silver nanoparticles (SSSNP) were selected as diffusible tracer, low-diffusible tracer, and non-diffusible nanoparticles, respectively, to perform transport experiments before and after the active 20-day bioreduction phase, with an aim of assessing the changes in soil structure and surface chemical properties resulting from Fe(III)-bioreduction. The transport of diffusible Br-was not influenced by the Fe(III)-bioreduction as evidenced by identical breakthrough curves before and after the introduction of acetate. Low-diffusible DFBA showed earlier breakthrough and less tailing after the bioreduction, suggesting alterations in flow paths and surface chemical properties of the soils. Similarly, non-diffusible SSSNP exhibited early breakthrough and enhanced transport after the bioreduction phase. Unexpectedly, the bioreduction caused complete retention of SSSNP in the soil columns when the acetate injection was extended from 20 days to 60 days, though no changes were observed for Br-and DFBA during the extended bioreduction period. The large change in the transport of SSSNP was attributed to the enhancement of soil aggregate breakdown and soil colloid release causing mechanical straining of SSSNP and the exposure of iron oxide surfaces previously unavailable within aggregate interiors favorable to the attachment of SSSNP. These results demonstrate that microbial activity can affect soil properties and transport behaviors of diffusivity-varying solutes and colloids in a time dependent fashion, a finding with implication for interpreting the data generated from soil column experiments under continuous flow.HighlightsFe(III)-bioreduction causes time-dependent aggregate breakdown and colloid release.Short-term bioreduction alters soil aggregate surface chemistry and tracer transport.Electron donor amendment enhances transport of nanoparticle tracer.


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