scholarly journals Soil microbial biomass in cropland and forest ecosystem in eastern Nepal

2013 ◽  
Vol 3 (1) ◽  
pp. 69-74
Author(s):  
T.N. Mandal

Soil microbial biomass carbon (MB-C) and nitrogen (MB-N) were estimated in some man-made cropland ecosystems and Sal forest natural ecosystem in eastern Nepal. In these cropping systems MB-C ranged between 244 µg g-1 and 425 µg g-1 soil, minimum in tea cultivation and maximum in uncultivated paddy field. MB –N ranged from 24.7 µg g-1 to 43.2 µg g-1 soil, which was minimum in paddy field at mature crop stage and maximum in uncultivated paddy field. Towards natural ecosystem five landslide damaged sites selected in Sal forest ecosystem were 1 yr., 4yr., 15yr., 40yr., and 58-year old. Under these sites MB-C was minimum (132μg g-1) in 1-yr old site and maximum (638 µg g-1) in 58- yr old site. Similarly, MB-N was also minimum (14 µg g-1) in 1-yr and maximum (55 µg g-1) in 58- yr old site. In comparison to undisturbed mature Sal forest 58 year old site showed 82 % recovery in soil microbial biomass which indicates the re-establishment of soil nutrients and restitution of nutrients cycling.

Forests ◽  
2018 ◽  
Vol 9 (9) ◽  
pp. 508 ◽  
Author(s):  
Zhiwei Ge ◽  
Shuiyuan Fang ◽  
Han Chen ◽  
Rongwei Zhu ◽  
Sili Peng ◽  
...  

Soil resident water-stable macroaggregates (diameter (Ø) > 0.25 mm) play a critical role in organic carbon conservation and fertility. However, limited studies have investigated the direct effects of stand development on soil aggregation and its associated mechanisms. Here, we examined the dynamics of soil organic carbon, water-stable macroaggregates, litterfall production, fine-root (Ø < 1 mm) biomass, and soil microbial biomass carbon with stand development in poplar plantations (Populus deltoides L. ‘35’) in Eastern Coastal China, using an age sequence (i.e., five, nine, and 16 years since plantation establishment). We found that the quantity of water-stable macroaggregates and organic carbon content in topsoil (0–10 cm depth) increased significantly with stand age. With increasing stand age, annual aboveground litterfall production did not differ, while fine-root biomass sampled in June, August, and October increased. Further, microbial biomass carbon in the soil increased in June but decreased when sampled in October. Ridge regression analysis revealed that the weighted percentage of small (0.25 mm ≤ Ø < 2 mm) increased with soil microbial biomass carbon, while that of large aggregates (Ø ≥ 2 mm) increased with fine-root biomass as well as microbial biomass carbon. Our results reveal that soil microbial biomass carbon plays a critical role in the formation of both small and large aggregates, while fine roots enhance the formation of large aggregates.


1996 ◽  
Vol 76 (4) ◽  
pp. 459-467 ◽  
Author(s):  
William R. Horwath ◽  
Eldor A. Paul ◽  
David Harris ◽  
Jeannette Norton ◽  
Leslie Jagger ◽  
...  

Chloroform fumigation-incubation (CFI) has made possible the extensive characterization of soil microbial biomass carbon (C) (MBC). Defining the non-microbial C mineralized in soils following fumigation remains the major limitation of CFI. The mineralization of non-microbial C during CFI was examined by adding 14C-maize to soil before incubation. The decomposition of the 14C-maize during a 10-d incubation after fumigation was 22.5% that in non-fumigated control soils. Re-inoculation of the fumigated soil raised 14C-maize decomposition to 77% that of the unfumigated control. A method was developed which varies the proportion of mineralized C from the unfumigated soil (UFC) that is subtracted in calculating CFI biomasss C. The proportion subtracted (P) varies according to a linear function of the ratio of C mineralized in the fumigated (FC) and unfumigated samples (FC/UFC) with two parameters K1 and K2 (P = K1FC/UFC) + K2). These parameters were estimated by regression of CFI biomass C, calculated according to the equation MBC = (FC − PUFC)/0.41, against that derived by direct microscopy in a series of California soils. Parameter values which gave the best estimate of microscopic biomass from the fumigation data were K1 = 0.29 and K2 = 0.23 (R2 = 0.87). Substituting these parameter values, the equation can be simplified to MBC = 1.73FC − 0.56UFC. The equation was applied to other CFI data to determine its effect on the measurement of MBC. The use of this approach corrected data that were previously difficult to interpret and helped to reveal temporal trends and changes in MBC associated with soil depth. Key words: Chloroform fumigation-incubation, soil microbial biomass, microscopically estimated biomass, carbon, control, 14C


2016 ◽  
Author(s):  
Marshall D. McDaniel ◽  
A. Stuart Grandy

Abstract. Agriculture-driven declines in plant biodiversity reduce soil microbial biomass, alter microbial functions, and threaten the provisioning of soil ecosystem services. We examined whether increasing temporal plant biodiversity (by rotating crops) can partially reverse these trends and enhance microbial biomass and function. We quantified seasonal patterns in soil microbial biomass, respiration rates, extracellular enzyme activity, and catabolic potential three times over one growing season in a 12-year crop rotation study at the W.K. Kellogg Biological Station LTER. Rotation treatments varied from one to five crops in a three-year rotation cycle, but all soils were sampled under corn to isolate historical rotation effects from current crop effects. Inorganic N, the stoichiometry of microbial biomass and dissolved organic C and N varied seasonally, likely reflecting fluctuations in soil resources during the growing season. Soils from biodiverse cropping systems increased microbial biomass C by 28–112 % and N by 18–58 % compared to monoculture corn. Rotations increased potential C mineralization by as much as 64 %, and potential N mineralization by 62 %, and both were related to substantially higher hydrolase and lower oxidase enzyme activities. The catabolic potential of the microbial community, assessed with community-level physiological profiling, showed that microbial communities in monoculture corn preferentially used simple substrates like carboxylic acids, relative to more diverse cropping systems. By isolating plant biodiversity from differences in fertilization and tillage, our study illustrates that crop biodiversity has overarching effects on soil microbial biomass and function that last throughout the growing season. In simplified agricultural systems, relatively small increases in plant biodiversity have a large impact on microbial community size and function.


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