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Decomposition of Main Litter Types and Nitrogen Release in Post-fire Larch Forests of the Russian Far East

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Abstract

Decomposition processes in larch forests, which occupy a significant part of the boreal zone and are most frequently affected by devastating ground fires, are poorly researched. In the course of a long-term (850 days) field experiment, the decomposition of litter types typical for boreal larch forests of the Russian Far East (needles, leaves, branches, and grass) was monitored in larch stands, both natural ones and those disturbed by fire. The following litter parameters were measured: mass loss, carbon (C) and nitrogen (N) dynamics, respiration, and environmental conditions (temperature and humidity). It is established that, 15 years after a long-lasting ground fire, the inflow of C and N with ground litter has decreased 2.2 times in comparison with the prefire level. At this stage of post-fire succession, the share of tree litter is lower, while the share of low-lignin grass litter is higher in comparison with the control. No differences in mass loss rates were identified between the studied stands for leaves, grass, and branches. However, at the end of the experiment (day 850, p = 0.0035), needles were decomposing more slowly in the burned larch forest than in the control. A lower CO2 emission intensity featured by the needle litter in the postfire forest (p = 0.0207) in comparison with the control and a lower nitrogen content in decomposing needles at later stages of the experiment (p = 0.0234) indicate that the post-fire factor inhibits microbiological activities. A decrease in the total N inflow with litter in the post-fire stand, combined with a lower needle decomposition rate, results in a slower release of nitrogen and its availability to plants and microorganisms, which may affect the restoration of boreal larch forest ecosystems damaged by fires.

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REFERENCES

  1. Abramova, E.R., Kondratova, A.V., Shumilova, L.P., and Piletskaya, O.A., Biological properties of soils in anthropogenically damaged boreal forests of Amur region, Mezhdunar. Nauchno-Issled. Zh., 2020, vol. 95, no. 5-1, pp. 162–167.

  2. Bani, A., Pioli, S., Ventura, M., Panzacchi, P., Borruso, L., Tognetti, R., and Brusetti, L., The role of microbial community in the decomposition of leaf litter and deadwood, Appl. Soil Ecol., 2018, vol. 126, pp. 75–84.

    Article  Google Scholar 

  3. Bazilevich, N.I., Titlyanova, A.A., Smirnov, V.V., Rodin, L.E., Nechaeva, N.T., and Levin, F.I., Metody izucheniya biologicheskogo krugovorota v razlichnykh prirodnykh zonakh (Analysis of Biological Cycle in Various Nature Zones), Rode, A.A., Ed., Moscow: Mysl’, 1978.

    Google Scholar 

  4. Beare, M.H., Neely, C.L., Coleman, D.C., and Hargrove, W.L., A substrate-induced respiration (SIR) method for measurement of fungal and bacterial biomass on plant residues, Soil Biol. Biochem., 1991, vol. 22, pp. 585–594.

    Article  Google Scholar 

  5. Berg, B., Litter decomposition and organic matter turnover in northern forest soils, For. Ecol. Manage., 2000, vol. 133, pp. 13–22.

    Article  Google Scholar 

  6. Berg, B. and McClaugherty, C., Plant Litter: Decomposition, Humus Formation, Carbon Sequestration, Berlin: Springer-Verlag, 2014, 3rd ed.

    Book  Google Scholar 

  7. Bryanin, S.V. and Abramova, E.S., Phytomass of litter fall in postfire larch forests of Zeisky Nature Reserve (Upper Amur region), Sib. Lesn. Zh., 2017, no. 2, pp. 93–101.

  8. Chigineva, N.I., Aleksandrova, A.V., Sidorova, I.I., and Tiunov, A.V., The effect of available carbon on microfungal community composition and decomposition rate of plant litter in soil, Mikol. Fitopatol., 2007, vol. 41, no. 5, pp. 428–435.

    Google Scholar 

  9. Dove, N.C. and Hart, S.C., Fire reduces fungal species richness and in situ mycorrhizal colonization: a meta-analysis, Fire Ecol., 2017, vol. 13, no. 2, pp. 37–65.

    Article  Google Scholar 

  10. García-Palacios, P., Shaw, E.A., Wall, D.H., and Hättenschwiler, S., Contrasting mass-ratio vs. niche complementarity effects on litter C and N loss during decomposition along a regional climatic gradient, J. Ecol., 2017, vol. 105, no. 4, pp. 968–978.

    Article  Google Scholar 

  11. Gartner, T.B. and Cardon, Z.G., Decomposition dynamics in mixed-species leaf litter, Oikos, 2004, vol. 104, no. 2, pp. 230–246.

    Article  Google Scholar 

  12. Gauthier, S., Bernier, P., Kuuluvainen, T., Shvidenko, A.Z., and Schepaschenko, D.G., Boreal forest health and global change, Science, 2015, vol. 349, no. 6250, pp. 819–822.

    Article  CAS  PubMed  Google Scholar 

  13. Gessner, M.O., Swan, C.M., Dang, C.K., McKie, B.G., Bardgett, R.D., Wall, D.H., et al., Diversity meets decomposition, Trends Ecol. Evol., 2010, vol. 25, no. 6, pp. 372–380.

    Article  PubMed  Google Scholar 

  14. Hart, S.C., DeLuca, T.H., Newman, G.S., MacKenzie, M.D., and Boyle, S.I., Post-fire vegetative dynamics as drivers of microbial community structure and function in forest soils, For. Ecol. Manage., 2005, vol. 220, nos. 1–3, pp. 166–184.

    Article  Google Scholar 

  15. Heim, A. and Frey, B., Early stage litter decomposition rates for Swiss forests, Biogeochemistry, 2004, vol. 70, no. 3, pp. 299–313.

    Article  CAS  Google Scholar 

  16. Hernandez, D.L. and Hobbie, S.E., Effects of fire frequency on oak litter decomposition and nitrogen dynamics, Oecologia, 2008, vol. 158, no. 3, pp. 535–543.

    Article  PubMed  Google Scholar 

  17. Hobbie, S.E. and Vitousek, P.M., Nutrient limitation of decomposition in Hawaiian montane forests, Ecology, 2000, vol. 81, no. 7, pp. 1867–1877.

    Article  Google Scholar 

  18. Holden, S.R., Gutierrez, A., and Treseder, K.K., Changes in soil fungal communities, extracellular enzyme activities, and litter decomposition across a fire chronosequence in Alaskan boreal forests, Ecosystems, 2013, vol. 16, no. 1, pp. 34–46.

    Article  CAS  Google Scholar 

  19. Horodecki, P. and Jagodziński, A.M., Site type effect on litter decomposition rates: a three-year comparison of decomposition process between spoil heap and forest sites, Forests, 2019, vol. 10, no. 4, pp. 353–374.

    Article  Google Scholar 

  20. IUSS Working Group, World Reference Base for Soil Resources 2014, Update 2015. International Soil Classification System for Naming Soils and Creating Legends for Soil Maps, World Soil Resources Reports No. 106, Rome: UN Food Agric. Org., 2015.

    Google Scholar 

  21. Johnstone, J.F., Hollingsworth, T.N., Chapin, F.S., and Mack, M.C., Changes in fire regime break the legacy lock on successional trajectories in Alaskan boreal forest, Global Change Biol., 2010, vol. 16, no. 4, pp. 1281–1295.

    Article  Google Scholar 

  22. Kelly, R., Chipman, M.L., Higuera, P.E., Stefanova, I., Brubaker, L.B., and Hu, F.S., Recent burning of boreal forest s exceeds fire regime limits of the past 10 000 years, Proc. Natl. Acad. Sci. U.S.A., 2013, vol. 110, no. 32, pp. 13055–13060.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. Kobak, K.I., Turchinovich, I.Y., Kondrasheva, N.Y., Schulze, E.D., Schulze, W., Koch, H., and Vygodskaya, N.N., Vulnerability and adaptation of the larch forest in eastern Siberia to climate change, Water, Air Soil Pollut., 1996, vol. 92, nos. 1–2, pp. 119–127.

    CAS  Google Scholar 

  24. Köster, K., Berninger, F., Heinonsalo, J., Linden, A., Köster, E., Ilvesniemi, H., and Pumpanen, J., The long-term impact of low-intensity surface fires on litter decomposition and enzyme activities in boreal coniferous forests, Int. J. Wildland Fire, 2016, vol. 25, no. 2, pp. 213–223.

    Article  Google Scholar 

  25. Liu, C., Liu, Y., Guo, K., Zhao, H., Qiao, X., Wang, S., Zhang, L., and Cai, X., Mixing litter from deciduous and evergreen trees enhances decomposition in a subtropical karst forest in southwestern China, Soil Biol. Biochem., 2016, vol. 101, pp. 44–54.

    Article  Google Scholar 

  26. Makita, N. and Fujii, S., Tree species effects on microbial respiration from decomposing leaf and fine root litter, Soil Biol. Biochem., 2015, vol. 88, pp. 39–47.

    Article  CAS  Google Scholar 

  27. Makita, N., Hirano, Y., Dannoura, M., Kominami, Y., Mizoguchi, T., Ishii, H., and Kanazawa, Y., Fine root morphological traits determine variation in root respiration of Quercus serrate, Tree Physiol., 2009, vol. 29, no. 4, pp. 579–585.

    Article  CAS  PubMed  Google Scholar 

  28. Monleon, V.J. and Cromack, K., Long-term effects of prescribed underburning on litter decomposition and nutrient release in ponderosa pine stands in central Oregon, For. Ecol. Manage., 1996, vol. 81, nos. 1–3, pp. 143–152.

    Article  Google Scholar 

  29. Olson, J.S., Energy storage and the balance of producers and decomposers in ecological systems, Ecology, 1963, vol. 44, no. 2, pp. 322–331.

    Article  Google Scholar 

  30. Palosuo, T., Liski, J., Trofymow, J.A., and Titus, B.D., Litter decomposition affected by climate and litter quality—Testing the Yasso model with litterbag data from the Canadian intersite decomposition experiment, Ecol. Model., 2005, vol. 189, nos. 1–2, pp. 183–198.

    Article  CAS  Google Scholar 

  31. Parton, W., Silver, W.L., Burke, I.C., Grassens, L., Harmon, M.E., Currie, W.S., King, J.Y., Adair, E.C., Brandt, L.A., Hart, S.C., and Fasth, B., Global-scale similarities in nitrogen release patterns during long-term decomposition, Science, 2007, vol. 315, no. 5810, pp. 361–364.

    Article  CAS  Google Scholar 

  32. Preston, C.M., Trofymow, J., et al., Variability in litter quality and its relationship to litter decay in Canadian forests, Can. J. Bot., 2000, vol. 78, no. 10, pp. 1269–1287.

    Google Scholar 

  33. R Development Core Team, R: a language and environment for statistical computing, 2017. https://www.r-project.org/.

  34. Rousk, J., Brookes, P.C., and Bååth, E., Contrasting soil pH effects on fungal and bacterial growth suggests functional redundancy in carbon mineralization, Appl. Environ. Microbiol., 2009, vol. 75, no. 6, pp. 1589–1596.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Sato, H., Kobayashi, H., Iwahana, G., and Ohta, T., Endurance of larch forest ecosystems in eastern Siberia under warming trends, Ecol. Evol., 2016, vol. 6, no. 16, pp. 5690–5704.

    Article  PubMed  PubMed Central  Google Scholar 

  36. Schweitzer, J.A., Bailey, J.K., Rehill, B.J., Martinsen, G.D., Hart, S.C., Lindroth, R.L., Keim, P., and Whitham, T.G., Genetically based trait in a dominant tree affects ecosystem processes, Ecol. Lett., 2004, vol. 7, no. 2, pp. 127–134.

    Article  Google Scholar 

  37. Seedre, M., Taylor, A.R., Brassard, B.W., Chen, H.Y.H., and Jõgiste, K., Recovery of ecosystem carbon stocks in young boreal forests: a comparison of harvesting and wildfire disturbance, Ecosystems, 2014, vol. 17, no. 5, pp. 851-863.

    Article  CAS  Google Scholar 

  38. Throop, H.L., Abu Salem, M., and Whitford, W.G., Fire enhances litter decomposition and reduces vegetation cover influences on decomposition in a dry woodland, Plant Ecol., 2017, vol. 218, no. 7, pp. 799–811.

    Article  Google Scholar 

  39. Vedrova, E.F. and Reshetnikova, T.V., Litter mass and intensity of litter decomposition in 40-year old plantations of the main forest forming species of Siberia, Lesovedenie, 2014, no. 1, pp. 42–50.

  40. Wang, X.L., Thompson, D.K., Marshall, G.A., Tymstra, C., Carr, R., and Flannigan, M.D., Increasing frequency of extreme fire weather in Canada with climate change, Clim. Change, 2015, vol. 130, no. 4, pp. 573-586.

    Article  Google Scholar 

  41. Zhang, W., Yang, K., Lyu, Z., and Zhu, J., Microbial groups and their functions control the decomposition of coniferous litter: a comparison with broadleaved tree litters, Soil Biol. Biochem., 2019, vol. 133, pp. 196–207.

    Article  CAS  Google Scholar 

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Funding

This study was supported by the Russian Foundation for Basic Research, project nos. 18-35-00454 and 19-05-00305.

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Authors and Affiliations

  1. Institute of Geology and Nature Management, Far East Branch, Russian Academy of Sciences, 675000, Blagoveshchensk, Russia

    A. V. Kondratova, E. R. Abramova & S. V. Bryanin

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  1. A. V. Kondratova
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  2. E. R. Abramova
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Correspondence to A. V. Kondratova.

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Translated by L. Emeliyanov

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Kondratova, A.V., Abramova, E.R. & Bryanin, S.V. Decomposition of Main Litter Types and Nitrogen Release in Post-fire Larch Forests of the Russian Far East. Contemp. Probl. Ecol. 14, 171–181 (2021). https://doi.org/10.1134/S1995425521020050

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