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Abstract AI-Helper 아이콘AI-Helper

Changes in the soil bacterial community of a coniferous forest were analyzed to assess microbial responses to wildfire. Soil samples were collected from three different depths in lightly and severely burned areas, as well as a nearby unburned control area. Direct bacterial counts ranged from $3...

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제안 방법

  • In order to analyze of the structure of the bacterial com­ munity by the FISH method, diluted soil suspensions were fixed by the addition of freshly-prepared 4% paraformaldehyde, and 30 μ 1 was passed through 0.2μm pore-sized polycarbonate filters. The filters were washed free of paraformaldehyde three times with 0.
  • , 2003). In this study, the microbial com­ munity of a coniferous forest's soil after a wildfire was monitored by direct counting and the FISH method, dur­ ing the 90 days after the fire. We have comparatively ana­ lyzed the effects of fire severity and soil depth on wildfire- induced changes in the microbial community.
  • As soil environments are quite heterogeneous in terms of texture, water content, and organic matter content, fire effects are highly variable, rendering the effects of fire on soil microbial communities even harder to examine and analyze. In this study, we monitored the soil bacterial community after wildfire by both direct counting, and the FISH method. It was dem­ onstrated that the wildfire affected mostly surface soil, and that the total bacterial population and bacterial com­ munity structure, after disruption by fire, began to recover quite quickly, such that the original level seemed to be restored only 3 months after the wildfire.
  • Oligonucleotide probes were commer­ cially constructed and labeled with tetramethylrhodamine (TaKaRa, Japan). The filter was placed on a gelatin- coated slide glass, and 16|11 of hybridization solution [0.9 M NaCl, 20 mM Tris-HCl (pH 7.4), 0.01% SDS, forma­ mide (concentrations for EUB, ALF, BET, GAM and CF were 0, 20, 35, 35, and 15%, respectively)] was added. At that time, 2111 of probe solution (25 ng) was added (Alfre­ ider et al.
  • 4 ha of forest was burned. The research areas were classified into lightly burned sites damaged by surface fire, severely burned sites damaged by crown fire, and the nearby control site, which was unaffected by wildfire. Each site was randomly divided into triplicate plots (10 mx 10 m each).

대상 데이터

  • Soil collection commenced on April 9, 17 days after the fire, and continued until July 5 (total 5 collections). From each plot, 3 random subsites were selected, ash and unburned plant residue was removed, and underlying soil was collected separately from the surface layer (0-5 cm depth), middle layer (6-15 cm) and deep layer (16-25 cm) soils.
  • The study area was a temperate coniferous forest (30-year old Pinus densiflora) located in Kangnung, Republic of Korea. The wildfire occurred on March 21-22, 2001 dur­ ing a dry spring, and 25.
  • It has been reported that remoistening increases the micro­ bial activity in dried soil, probably by the liberation of absorbed organic nutrients (Stevenson, 1956). The study area, located in the eastern Taebaek Mountain region, was experiencing very dry weather due to the Fohn phenom­ enon, which leads to low precipitation. Therefore, the microflora in the dry soil of this area might have been sig­ nificantly affected by this rainfall.
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참고문헌 (28)

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  3. Ahn, T., J. Lee, D. Lee, and H. Song. 2002. Ecological monitoring of soil microbial community after forest fire, p. 144-175. In Proceedings of Symposium on Prevention of large forest fire and remediation of ecosystem. Korea Forest Research Institute, Seoul, Korea 

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  12. Hicks, R., R. A $\beta$ mann, and D. Stahl. 1992. Dual staining of natural bacterioplankton with 4, 6-diamidino-2-phenylindole and fluorescent oligonucleotide probes targeting kingdom level 16S rRNA sequences. Appl. Environ. Microbiol. 58, 2158-2163. 

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  17. Madigan, M., J. Martinko, and J. Parker. 2003. Brock Biology of Microorganisms, p. A5-A13. Prentice Hall, Upper Saddle River 

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  20. Neary, D., C. Klopatek, L. DeBano, and P. Ffolliott. 1999. Fire effects on belowground sustainability: a review and synthesis. Forest Ecol. Manage. 122, 51-71 

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  23. Swift, L., K. Elliott, R. Ottmar, and R. Vihnanek. 1993. Site preparation burning to improve Southern Appalachian pine-hardwood stands: fire characteristics and soil erosion, moisture, and temperature. Can. J. Forest Res. 23, 2242-2254 

  24. Trebesius, K., R. Amann, W. Ludwig, K. Muhlegger, and K. Schleifer. 1994. Identification of whole fixed bacterial cells with nonradioactive rRNA targeted transcript probes. Appl. Environ. Microbiol. 60, 3228-3235 

  25. Vasander, H. and T. Lindholm. 1985. Fire intensities and surface temperatures during prescribed burning. Silva Fennica. 19, 1-15 

  26. Vazquez, F., M. Acea, and T. Carballas. 1993. Soil microbial populations after wildfire. FEMS Microbiol. Ecol. 13, 93-104 

  27. Wackett, L. and C. Hershberger. 2001. Biocatalysis and Biodegradation : Microbial transformation of organic compounds, p. 39-69. ASM Press, Washington, D.C. 

  28. Walstad, J., S. Radosevich, and D. Sandberg. 1990. Introduction to natural and prescribed fire in Pacific Northwest forests, p. 3-5. In J.D. Walstad, S.R. Radosevich, and D.V. Sandberg (eds.), Natural and Prescribed Fire in Pacific Northwest Forests Oregon State University Press, Corvallis. 

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