Journal of Ecology and Environment

The Ecological Society of Korea (한국생태학회)
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Effects of thinning intensity on nutrient concentration and enzyme activity in Larix kaempferi forest soils

  • Kim, Seongjun (Department of Environmental Science and Ecological Engineering, Graduate School, Korea University) ;
  • Han, Seung Hyun (Department of Environmental Science and Ecological Engineering, Graduate School, Korea University) ;
  • Li, Guanlin (Department of Environmental Science and Ecological Engineering, Graduate School, Korea University) ;
  • Yoon, Tae Kyung (Environmental Planning Institute, Seoul National University) ;
  • Lee, Sang-Tae (Forest Practice Research Center, National Institute of Forest Science) ;
  • Kim, Choonsig (Department of Forest Resources, Gyeongnam National University of Science and Technology) ;
  • Son, Yowhan (Department of Environmental Science and Ecological Engineering, Graduate School, Korea University)
  • Received : 2016.09.01
  • Accepted : 2016.09.14
  • Published : 2016.10.31
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Abstract

Background: As the decomposition of lignocellulosic compounds is a rate-limiting stage in the nutrient mineralization from organic matters, elucidation of the changes in soil enzyme activity can provide insight into the nutrient dynamics and ecosystem functioning. The current study aimed to assess the effect of thinning intensities on soil conditions. Un-thinned control, 20 % thinning, and 30 % thinning treatments were applied to a Larix kaempferi forest, and total carbon and nitrogen, total carbon to total nitrogen ratio, extractable nutrients (inorganic nitrogen, phosphorus, calcium, magnesium, potassium), and enzyme activities (acid phosphatase, ${\beta}$-glucosidase, ${\beta}$-xylosidase, ${\beta}$-glucosaminidase) were investigated. Results: Total carbon and nitrogen concentrations were significantly increased in the 30 % thinning treatment, whereas both the 20 and 30 % thinning treatments did not change total carbon to total nitrogen ratio. Inorganic nitrogen and extractable calcium and magnesium concentrations were significantly increased in the 20 % thinning treatment; however, no significant changes were found for extractable phosphorus and potassium concentrations either in the 20 or the 30 % thinning treatment. However, the applied thinning intensities had no significant influences on acid phosphatase, ${\beta}$-glucosidase, ${\beta}$-xylosidase, and ${\beta}$-glucosaminidase activities. Conclusions: These results indicated that thinning can elevate soil organic matter quantity and nutrient availability, and different thinning intensities may affect extractable soil nutrients inconsistently. The results also demonstrated that such inconsistent patterns in extractable nutrient concentrations after thinning might not be fully explained by the shifts in the enzyme-mediated nutrient mineralization.

Keywords

References

  1. Attiwill, P. M., & Adams, M. A. (1993). Nutrient cycling in forests. New Phytologist, 124, 561-582. https://doi.org/10.1111/j.1469-8137.1993.tb03847.x
  2. Grigal, D. F. (2000). Effects of extensive forest management on soil productivity. Forest Ecology and Management, 138, 167-185. https://doi.org/10.1016/S0378-1127(00)00395-9
  3. Boerner, R. E. J., Giai, C., Huang, J., & Miesel, J. R. (2008). Initial effects of fire and mechanical thinning on soil enzyme activity and nitrogen transformations in eight North American forest ecosystems. Soil Biology and Biochemistry, 40, 3076-3085. https://doi.org/10.1016/j.soilbio.2008.09.008
  4. Achat, D. L., Deleuze, C., Landmann, G., Pousse, N., Ranger, J., & Augusto, L. (2015). Quantifying consequences of removing harvesting residues on forest soils and tree growth-a meta-analysis. Forest Ecology and Management, 348, 124-141. https://doi.org/10.1016/j.foreco.2015.03.042
  5. Son, Y., Jun, Y. C., Lee, Y. Y., Kim, R. H., & Yang, S. Y. (2004). Soil carbon dioxide evolution, litter decomposition, and nitrogen availability four years after thinning in a Japanese larch plantation. Communications in Soil Science and Plant Analysis, 35, 1111-1122. https://doi.org/10.1081/CSS-120030593
  6. Masyagina, O. V., Hirano, T., Ji, D. H., Choi, D. S., Qu, L., Fujinuma, Y., Sasa, K., Matsuura, Y., Prokushkin, S. G., & Koike, T. (2006). Effect of spatial variation of soil respiration rates following disturbance by timber harvesting in a larch plantation in northern Japan. Forest Science and Technology, 2, 80-91. https://doi.org/10.1080/21580103.2006.9656303
  7. Smolander, A., Kitunen, V., Kukkola, M., & Tamminen, P. (2013). Response of soil organic matter layer characteristics to logging residues in three Scots pine thinning stands. Soil Biology and Biochemistry, 66, 51-59. https://doi.org/10.1016/j.soilbio.2013.06.017
  8. Hwang, J., & Son, Y. (2006). Short-term effects of thinning and liming on forest soils of pitch pine and Japanese larch plantations in central Korea. Ecological Research, 21, 671-680. https://doi.org/10.1007/s11284-006-0170-1
  9. Kim, S., Yoon, T. K., Han, S., Han, S. H., Lee, J., Kim, C., Lee, S.-T., Seo, K. W., Yang, A.-R., & Son, Y. (2015). Initial effects of thinning on soil carbon storage and base cations in a naturally regenerated Quercus spp. forest in Hongcheon, Korea. Forest Science and Technology, 11, 172-176. https://doi.org/10.1080/21580103.2014.957357
  10. Giai, C., & Boerner, R. E. J. (2007). Effects of ecological restoration on microbial activity, microbial functional diversity, and soil organic matter in mixed-oak forests of southern Ohio, USA. Applied Soil Ecology, 35, 281-290. https://doi.org/10.1016/j.apsoil.2006.08.003
  11. Adamczyk, B., Adamczyk, S., Kukkola, M., Tamminen, P., & Smolander, A. (2015). Logging residue harvest may decrease enzymatic activity of boreal forest soils. Soil Biology and Biochemistry, 82, 74-80. https://doi.org/10.1016/j.soilbio.2014.12.017
  12. Sinsabaugh, R. L., Lauber, C. L., Weintraub, M. N., Ahmed, B., Allison, S. D., Crenshaw, C., Contosta, A. R., Cusack, D., Frey, S., Gallo, M. E., Gartner, T. B., Hobbie, S. E., Holland, K., Keeler, B. L., Powers, J. S., Stursova, M., Takacs-Vesbach, C., Waldrop, M. P., Wallenstein, M. D., Zak, D. R., & Zeglin, L. H. (2008). Stoichiometry of soil enzyme activity at global scale. Ecology Letters, 11, 1252-1264. https://doi.org/10.1111/j.1461-0248.2008.01245.x
  13. Korea Forest Service. (2015). Statistical yearbook of forestry. Daejeon: Korea Forest Service. (In Korean).
  14. Hwang, J., Son, Y., Kim, C., Yi, M.-J., Kim, Z.-S., Lee, W.-K., & Hong, S.-K. (2007). Fine root dynamics in thinned and limed pitch pine and Japanese larch plantations. Journal of Plant Nutrition, 30, 1821-1839. https://doi.org/10.1080/01904160701628940
  15. Lee, S. K., Son, Y., Lee, W. K., Yang, A.-R., Noh, N. J., & Byun, J.-G. (2010). Influence of thinning on carbon storage in a Japanese larch (Larix kaempferi) plantation in Yangpyeong, central Korea. Forest Science and Technology, 6, 35-40. https://doi.org/10.1080/21580103.2010.9656356
  16. Ko, S., Son, Y., Noh, N. J., Yoon, T. K., Kim, C., Bae, S.-W., Hwang, J., Lee, S.-T., & Kim, H.-S. (2012). Influence of thinning on carbon storage in soil, forest floor and coarse woody debris of Larix kaempferi stands in Korea. Forest Science and Technology, 8, 116-121. https://doi.org/10.1080/21580103.2012.672018
  17. Baldrian, P., & Stursova, M. (2011). Enzymes in forest soils. In G. Shukla & A. Varma (Eds.), Soil enzymology (pp. 61-73). Heidelberg: Springer.
  18. Olander, L. P., & Vitousek, P. M. (2000). Regulation of soil phosphatase and chitinase activity by N and P availability. Biogeochemistry, 49, 175-190. https://doi.org/10.1023/A:1006316117817
  19. Tabatabai, M. A., Ekenler, M., & Senwo, Z. N. (2010). Significance of enzyme activities in soil nitrogen mineralization. Communications in Soil Science and Plant Analysis, 41, 595-605. https://doi.org/10.1080/00103620903531177
  20. Kim, S., Han, S. H., Lee, J., Kim, C., Lee, S.-T., & Son, Y. (2016). Impact of thinning on carbon storage of dead organic matter across larch and oak stands in South Korea. iForest, 9, 593-598. https://doi.org/10.3832/ifor1776-008
  21. Park, C.-W., Ko, S., Yoon, T. K., Han, S., Yi, K., Jo, W., Jin, L., Lee, S. J., Noh, N. J., Chung, H., & Son, Y. (2011). Differences in soil aggregate, microbial biomass carbon concentration, and soil carbon between Pinus rigida and Larix kaempferi plantations in Yangpyeong, central Korea. Forest Science and Technology, 8, 38-46.
  22. Mulvaney, R. L. (1996). Nitrogen-inorganic forms. In D. L. Sparks, P. A. Helmke, R. H. Loeppert, P. N. Soltanpour, M. A. Tabatabai, C. T. Johnston, & M. E. Sumner (Eds.), Methods of soil analysis. Part 3-chemical methods (pp. 1146-1155). Madison: Soil Sci Soc Am.
  23. Miranda, K. M., Espey, M. G., & Wink, D. A. (2001). A rapid, simple spectrophotometric method for simultaneous detection of nitrate and nitrite. Nitric Oxide, 5, 62-71. https://doi.org/10.1006/niox.2000.0319
  24. Bray, R. H., & Kurtz, L. T. (1945). Determination of total, organic, and available forms of phosphorus in soils. Soil Science, 59, 39-46. https://doi.org/10.1097/00010694-194501000-00006
  25. DeForest, J. L. (2009). The influence of time, storage temperature, and substrate age on potential soil enzyme activity in acidic forest soils using MUB-linked substrates and L-DOPA. Soil Biology and Biochemistry, 41, 1180-1186. https://doi.org/10.1016/j.soilbio.2009.02.029
  26. Hodge, A., Robinson, D., & Fitter, A. (2000). Are microorganisms more effective than plants at competing for nitrogen? Trends in Plant Science, 5, 304-308. https://doi.org/10.1016/S1360-1385(00)01656-3
  27. Siemion, J., Burns, D. A., Murdoch, P. S., & Germain, R. H. (2011). The relation of harvesting intensity to changes in soil, soil water, and stream chemistry in a northern hardwood forest, Catskill Mountains, USA. Forest Ecology and Management, 261, 1510-1519. https://doi.org/10.1016/j.foreco.2011.01.036
  28. Chen, X.-L., Wang, D., Chen, X., Wang, J., Diao, J.-J., Zhang, J.-Y., & Guan, Q.-W. (2015). Soil microbial functional diversity and biomass as affected by different thinning intensities in a Chinese fir plantation. Applied Soil Ecology, 92, 35-44. https://doi.org/10.1016/j.apsoil.2015.01.018
  29. Karaca, A., Cetin, S. C., Turgay, O. C., & Kizilkaya, R. (2011). Soil enzymes as indication of soil quality. In G. Shukla & A. Varma (Eds.), Soil enzymology (pp. 119-148). Heidelberg: Springer.
  30. Brzostek, E. R., Greco, A., Drake, J. E., & Finzi, A. C. (2013). Root carbon inputs to the rhizosphere stimulate extracellular enzyme activity and increase nitrogen availability in temperate forest soils. Biogeochemistry, 115, 65-76. https://doi.org/10.1007/s10533-012-9818-9
  31. Boyle, S. I., Hart, S. C., Kaye, J. P., & Waldrop, M. P. (2005). Restoration and canopy type influence soil microflora in a ponderosa pine forest. Soil Science Society of America Journal, 69, 1627-1638. https://doi.org/10.2136/sssaj2005.0029
  32. Maassen, S., Fritze, H., & Wirth, S. (2006). Response of soil microbial biomass, activities, and community structure at a pine stand in northeastern Germany 5 years after thinning. Can J of For Res., 36, 1427-1434. https://doi.org/10.1139/x06-039
  33. Geng, Y., Dighton, J., & Gray, D. (2012). The effects of thinning and soil disturbance on enzyme activities under pitch pine soil in New Jersey pinelands. Applied Soil Ecology, 62, 1-7. https://doi.org/10.1016/j.apsoil.2012.07.001

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