Contribution of soil fauna to the degradation of recalcitrant components in Cinnamomum camphora foliar litter in different-sized gaps in Pinus massoniana plantations

Yan Zhang , Danju Zhang , Xun Li , Jian Zhang

Journal of Forestry Research ›› 2019, Vol. 30 ›› Issue (3) : 931 -941.

PDF
Journal of Forestry Research ›› 2019, Vol. 30 ›› Issue (3) : 931 -941. DOI: 10.1007/s11676-018-0609-6
Original Paper

Contribution of soil fauna to the degradation of recalcitrant components in Cinnamomum camphora foliar litter in different-sized gaps in Pinus massoniana plantations

Author information +
History +
PDF

Abstract

Forest gaps are important in forest dynamics and management, but little is known about how soil fauna influence the degradation of recalcitrant litter components in different-sized forest gaps. This investigation uses litterbags with two different mesh sizes (0.04 and 3 mm) to control the meso- and microfauna entering the bags to quantify the contribution of soil fauna to the degradation of recalcitrant components (including condensed tannins, total phenol, lignin and cellulose) during litter decomposition. The experiment was conducted in seven different forest gap sizes in Pinus massoniana plantations over 1 year. One closed-canopy site (CC) and forest gap sizes of 100, 225, 400, 625, 900, 1225 and 1600 m2 were created in a P. massoniana plantation in the Sichuan basin of China; the CC was treated as the control. Cinnamomum camphora foliage from local native trees was used in all forest gap experiments. We found the following: (1) Gap size had significant effects on the degradation rates (E) of condensed tannins and lignin and on the contributions of soil fauna; medium-sized gaps also presented high degradation rates. Soil fauna obviously contributed to the degradation of recalcitrant foliar litter components in medium-sized gaps. (2) The highest contribution to degradation (40.98%) was recorded for lignin, and the lowest contribution (0.29%) was recorded for condensed tannins. The results indicate that medium-sized gaps (900 m2) were conducive to the degradation of recalcitrant litter components by soil fauna.

Keywords

Cinnamomum camphora / Foliar litter / Gap size / Pinus massoniana / Recalcitrant litter components / Soil fauna

Cite this article

Download citation ▾
Yan Zhang, Danju Zhang, Xun Li, Jian Zhang. Contribution of soil fauna to the degradation of recalcitrant components in Cinnamomum camphora foliar litter in different-sized gaps in Pinus massoniana plantations. Journal of Forestry Research, 2019, 30(3): 931-941 DOI:10.1007/s11676-018-0609-6

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Arunachalam A, Arunachalam K. Influence of gap size and soil properties on microbial biomass in a subtropical humid forest of north-east india. Plant Soil, 2000, 223(1–2): 187-195.

[2]

Austin AT, Ballaré CL. Dual role of lignin in plant litter decomposition in terrestrial ecosystems. Proc Natl Acad Sci USA, 2010, 107(10): 4618-4622.

[3]

Berg B. Litter decomposition and organic matter turnover in northern forest soils. For Ecol Manag, 2000, 133(1): 13-22.

[4]

Berg B, Mcclaugherty C. Plant litter. Decomposition, humus formation, carbon sequestration, 2013 2 Berlin: Springer.

[5]

Bjorn B. Litter decomposition: a guide to carbon and nutrient turnover, 2006, Amsterdam: Elsevier Academic Press 1 448

[6]

Booker FL, Maier CA. Atmospheric carbon dioxide, irrigation, and fertilization effects on phenolic and nitrogen concentrations in loblolly pine (Pinus taeda) needles. Tree Physiol, 2001, 21(9): 609-616.

[7]

Brandt LA, King JY, Hobbie SE, Milchunas DG, Sinsabaugh RL. The role of photodegradation in surface litter decomposition across a grassland ecosystem precipitation gradient. Ecosystems, 2010, 13(5): 765-781.

[8]

Butter NL, Dawson JM, Wakelin D, Buttery PJ. Effect of dietary condensed tannins on gastrointestinal nematodes. J Agric Sci, 2001, 137(12): 461-469.

[9]

Canham CD, Marks PL (1985) The response of woody plants to disturbance: patterns of establishment and growth, chap 11. The Ecology of Natural Disturbance and Patch Dynamics, pp 197–216

[10]

Carrillo Y, Ball BA, Bradford MA, Jordan CF, Molina M. Soil fauna alter the effects of litter composition on nitrogen cycling in a mineral soil. Soil Biol Biochem, 2011, 43(7): 1440-1449.

[11]

Clein JS, Schimel JP. Microbial activity of tundra and taiga soils at sub-zero temperatures. Soil Biol Biochem, 1995, 27: 1231-1234.

[12]

Compiled by Team of Handbook of Soil Fauna Research Methods, Handbook of Soil Fauna Research Methods, China forest Press, Beijing, 1998

[13]

Connell JH. Diversity in tropical rain forests and coral reefs. Science, 1978, 199: 1302-1310.

[14]

Cui NJ, Liu Y, Zhang J, Yang WQ, Ou J, Zhang J, Deng CC, Li JP. Effects of forest gap on plant diversity of Pinus massoniana plantations. Chin J Appl Environ Biol, 2014, 20(1): 8-14. (in Chinese)

[15]

Cui NJ, Zhang DJ, Liu Y, Zhang J, Yang WQ, Ou J, Zhang J, Song XY, Yin R. Plant diversity and seasonal dynamics in forest gaps of varying sizes in Pinus massoniana plantation. Chin J Plant Ecol, 2014, 38(5): 477-490. in Chinese)

[16]

David JF. The role of litter-feeding macroarthropods in decomposition processes: a reappraisal of common views. Soil Biol Biochem, 2014, 76: 109-118.

[17]

Devagiri GM, Khaple AK, Mohan S, Venkateshamurthy P, Tomar S, Arunkumar AN, Joshi G. Species diversity, regeneration and dominance as influenced by canopy gaps and their characteristics in tropical evergreen forests of western ghats, india. J For Res, 2016, 27(4): 799-810.

[18]

FAO (2007) The state of the world’s forests. ftp.fao.org/docrep/fao/009. FAO, Rome, Italy

[19]

Gálhidy L, Mihók B, Hagyó A, Rajkai K, Standovár T. Effects of gap size and associated changes in light and soil moisture on the understorey vegetation of a Hungarian beech forest. Plant Ecol, 2006, 183: 133-145.

[20]

Gallo ME, Porras-Alfaro A, Odenbach KJ, Sinsabaugh RL. Photoacceleration of plant litter decomposition in an arid environment. Soil Biol Biochem, 2009, 41(7): 1433-1441.

[21]

García-Palacios P, Maestre FT, Kattge J, Wall DH. Climate and litter quality differently modulate the effects of soil fauna on litter decomposition across biomes. Ecol Lett, 2013, 16(8): 1045-1053.

[22]

Gebauer RLE, Strain BR, Reynolds JF. The effect of elevated CO2 and N availability on tissue concentrations and whole plant pools of carbon-based secondary compounds in loblolly pine (pinus taeda). Oecologia, 1998, 113(1): 29-36.

[23]

Gong ZT. The Chinese soil classification system, 1999, Beijing: Science Press (in Chinese)

[24]

Graça MAS, Bärlocher F, Gessner MO. Methods to study litter decomposition: a practical guide, 2005, New York: Springer.

[25]

Gray AN, Spies TA, Easter MJ. Microclimatic and soil moisture responses to gap formation in coastal Douglas-fir forests. Can J For Res, 2011, 32(2): 332-343.

[26]

Herman J, Moorhead D, Berg B. The relationship between rates of lignin and cellulose decay in aboveground forest litter. Soil Biol Biochem, 2008, 40(10): 2620-2626.

[27]

Hill SB, Mallik AU, Chen HY. Canopy gap disturbance and succession in trembling aspen dominated boreal forests in Northeastern Ontario. Can J For Res, 2005, 35(8): 1942-1951.

[28]

Kalbitz K, Solinger S, Park JH, Michalzik B, Matzner E. Controls on the dynamics of dissolved organic matter in soils: a review. Soil Sci, 2000, 165(4): 277-304.

[29]

Kraus TEC, Yu ZC, Preston CM, Dahlgren RA, Zasoski RJ. Linking chemical reactivity and protein precipitation to structural characteristics of foliar tannins. J Chem Ecol, 2003, 29(3): 703-730.

[30]

Li Z-Y, Wang Y-H, Yu P-T, Zhang Z-J. A comparative study of resistance to soil acidification and growth of fine roots between pure stands of Pinus massoniana and Cinnamomum camphora. Acta Ecol Sin, 2007, 27(12): 5245-5253.

[31]

Lu RK. Soil and agro-chemical analytical method, 1999, Beijing: China Agricultural Science and Technology Press (in Chinese)

[32]

Mallik AU, Kreutzweiser DP, Spalvieri CM. Forest regeneration in gaps seven years after partial harvesting in riparian buffers of boreal mixedwood streams. For Ecol Manag, 2014, 312(1): 117-128.

[33]

McCarthy J. Gap dynamics of forest trees: a review with particular attention to boreal forests. Environ Rev, 2001, 9: 1-59.

[34]

Mohamed ASA, Mori T, Islam SQ, Sato M, Yamasaki T. Lethal activity of gallo- and condensed tannins against the free-living soil-inhabiting nematode, Caenorhabditis elegans. J Pestic Sci, 2000, 25: 410-415.

[35]

Mole S, Ross JA, Waterman PG. Light-induced variation in phenolic levels in foliage of rain-forest plants: i. Chemical changes. J Chem Ecol, 1988, 14(1): 1-21.

[36]

Muscolo A, Sidari M, Mercurio R. Influence of gap size on organic matter decomposition, microbial biomass and nutrient cycle in Calabrian pine (pinus laricio, poiret) stands. For Ecol Manag, 2007, 242(2): 412-418.

[37]

Ou J, Zhang J, Cui NJ, Chen YM, Zhang J, Yang WQ, Liu Y. The early effects of forest gap harvesting on soil microbial biomass in Pinus massoniana plantations. J Nat Resour, 2014, 29(12): 2036-2047. (in Chinese)

[38]

Parfitt RL, Newman RH. 13C NMR study of pine needle decomposition. Plant Soil, 2000, 219(1–2): 273-278.

[39]

Peng Y, Yang W, Li J, Wang B, Zhang C, Yue K, Wu F. Contribution of soil fauna to foliar litter-mass loss in winter in an ecotone between dry valley and montane forest in the upper reaches of the minjiang river. PLoS ONE, 2015 10 4 e0124605

[40]

Pflug A, Wolters V. Influence of drought and litter age on Collembola communities. Eur J Soil Biol, 2001, 37(4): 305-308.

[41]

Prescott CE. The influence of the forest canopy on nutrient cycling. Tree Physiol, 2002, 22: 1193-1200.

[42]

Prescott CE, Hope GD, Blevins LL. Effect of gap size on litter decomposition and soil nitrate concentrations in a high-elevation spruce-fir forest. Can J For Res, 2003, 339(11): 2210-2220.

[43]

Rahman MM, Tsukamoto J, Rahman MM, Yoneyama A, Mostafa KM. Lignin and its effects on litter decomposition in forest ecosystems. Chem Ecol, 2013, 29(6): 540-553.

[44]

Richardson BA, Richardson MJ, González G, Shiels AB, Srivastava DS. A canopy trimming experiment in Puerto Rico: the response of litter invertebrate communities to canopy loss and debris deposition in a tropical forest subject to hurricanes. Ecosystems, 2010, 13: 286-301.

[45]

Ritter E. Litter decomposition and nitrogen mineralization in newly formed gaps in a Danish beech (Fagus sylvatica) forest. Soil Biol Biochem, 2005, 37(7): 1237-1247.

[46]

Schwarz W. The cellulosome and cellulose degradation by anaerobic bacteria. Appl Microbiol Biotechnol, 2001, 56(5–6): 634-649.

[47]

Seibold S, Bässler C, Baldrian P, Reinhard L, Thorn S, Ulyshen MD, Weiß I, Müller J. Dead-wood addition promotes non-saproxylic epigeal arthropods but effects are mediated by canopy openness. Biol Cons, 2016, 204: 181-188.

[48]

Song XZ, Jiang H, Zhang HL, Peng CH, Yu SQ. Elevated UV-B radiation did not affect decomposition rates of needles of two coniferous species in subtropical china. Eur J Soil Biol, 2011, 47(6): 343-348.

[49]

Stout RJ. Effects of condensed tannins on leaf processing in mid-latitude and tropical streams: a theoretical approach. Can J Fish Aquat Sci, 1989, 46(7): 1097-1106.

[50]

Swift MJ, Heal OW, Anderson JM. Decomposition in terrestrial ecosystems, 1979, Berkeley: University of California Press.

[51]

Terrill TH, Rowan AM, Douglas GB, Barry TN. Determination of extractable and bound condensed tannin concentrations in forage plants, protein concentrate meals and cereal grains. J Sci Food Agric, 1992, 58(3): 321-329.

[52]

Valachovic YS, Caldwell BA, Cromack K, Griffiths RP. Leaf litter chemistry controls on decomposition of pacific northwest trees and woody shrubs. Can J For Res, 2004, 34(10): 2131-2147.

[53]

Wang SJ, Ruan HH, Han Y. Effects of microclimate, litter type, and mesh size on leaf litter decomposition along an elevation gradient in the Wuyi Mountains, China. Ecol Res, 2010, 25: 1113-1120.

[54]

Whitmore T. Canopy gaps and the two major groups of forest trees. Ecology, 1989, 70: 536-538.

[55]

Xin WD, Yin XQ, Song B. Contribution of soil fauna to litter decomposition in Songnen sandy lands in Northeastern China. J Arid Environ, 2012, 77(1): 90-95.

[56]

Xu JX, Lie GW, Xue L. Effects of gap size on diversity of soil fauna in a cunninghamia lanceolata stand damaged by an ice storm in southern china. J For Res, 2016, 27(6): 1427-1434.

[57]

Yang XD, Jin C. Plant litter quality influences the contribution of soil fauna to litter decomposition in humid tropical forests, southwestern china. Soil Biol Biochem, 2009, 41(5): 910-918.

[58]

Yang Z, Liu JA, Zhou G, Yi WU, Deng X, Yan F. Community succession characteristics of Pinus massoninana plantation in Hengshan. For Resour Manag, 2012, 2(1): 42-47.

[59]

Yi H, Moldenke A. Responses of litter-dwelling arthropods to four different thinning intensities in Douglas-fir forests of the Pacific Northwest, USA. Ann Zool Fenn, 2008, 45: 229-240.

[60]

Yin WY, Hu SH, ShenYF Ning YZ, Sun XD, Wu JH, Zhuge Y, Zhang YM, Wang M, Chen JY, Xu CG, Liang YL, Wang HZ, Yang T, Chen DN, Zhang GQ, Song DX, Chen J, Liang LR, Hu CY, Wang HF, Zhang CZ, Kuang BR, Chen GX, Zhao LJ, Xie RD, Zhang J, Liu XW, Han MZ, Bi DY, Xiao NN, Yang DR. Pictorial keys to soil animals of China, 1998, Beijing: Science Press.

[61]

Yin XQ, Song B, Dong WH, Xin WD, Wang YQ. A review on the eco-geography of soil fauna in China. J Geog Sci, 2010, 20(3): 333-346.

[62]

Zhang QS, Liang YW. Effects of gap size on nutrient release from plant litter decomposition in a natural forest ecosystem. Can J For Res, 1995, 25: 1627-1638.

[63]

Zhang Q, Zak JC. Effects of gap size on litter decomposition and microbial activity in a subtropical forest. Ecology, 1995, 76(7): 2196-2204.

[64]

Zhang Q, Zak JC. Potential physiological activities of fungi and bacteria in relation to plant litter decomposition along a gap size gradient in a natural subtropical forest. Microb Ecol, 1998, 35(1): 172-179.

[65]

Zhou HC, Wei SD, Zeng Q, Zhang LH, Tam FY, Lin YM. Nutrient and caloric dynamics in avicennia marina leaves at different developmental and decay stages in Zhangjiang River Estuary, China. Estuar Coast Shelf Sci, 2010, 87(1): 21-26.

[66]

Zhu JX, Yang WQ, He XH. Temporal dynamics of abiotic and biotic factors on leaf litter of three plant species in relation to decomposition rate along a subalpine elevation gradient. PLoS ONE, 2013 8 4 e62073

AI Summary AI Mindmap
PDF

274

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/