Considerable impacts of litter inputs on soil nematode community composition in a young Acacia crassicapa plantation

Cancan Zhao, Yin Li, Chenlu Zhang, Yuan Miao, Mengzhou Liu, Wanlin Zhuang, Yuanhu Shao, Weixin Zhang, Shenglei Fu

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Soil Ecology Letters ›› 2021, Vol. 3 ›› Issue (2) : 145-155. DOI: 10.1007/s42832-021-0085-3
RESEARCH ARTICLE
RESEARCH ARTICLE

Considerable impacts of litter inputs on soil nematode community composition in a young Acacia crassicapa plantation

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Highlights

• Nematodes was investigated in a young Acacia crassicapa plantation in southern China

• Both litter addition and root presence enhanced soil nematode abundance

• Litter addition significantly altered soil nematode community composition

• Root presence had a limited impact on nematode trophic group composition

Abstract

Aboveground litter inputs and root exudates provide basal resources for soil communities, however, their relative contributions to soil food web are still not well understood. Here, we conducted a field manipulative experiment to differentiate the effects of litter inputs and living root on nematode community composition of surface and subsoils in a young Acacia crassicapa plantation in southern China. Our results showed that both litter addition and root presence significantly enhanced soil nematode abundance by 17.3% and 35.3%, respectively. Litter addition altered nematode trophic group composition, decreased fungivore to bacterivore ratio, and enhanced maturity index and structure index, which led to a bacterial-based energy channel and a more complex food web structure. However, root presence had a limited impact on the nematode community composition and ecological indices. Despite nematodes surface assembly, soil depth did not affect nematode trophic group composition or ecological index. Our findings highlight the importance of litter inputs in shaping soil nematode community structure and regulating soil energy channel.

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Keywords

Litter addition / Root exudates / Nematode community composition / Soil depth / Nematode ecological index

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Cancan Zhao, Yin Li, Chenlu Zhang, Yuan Miao, Mengzhou Liu, Wanlin Zhuang, Yuanhu Shao, Weixin Zhang, Shenglei Fu. Considerable impacts of litter inputs on soil nematode community composition in a young Acacia crassicapa plantation. Soil Ecology Letters, 2021, 3(2): 145‒155 https://doi.org/10.1007/s42832-021-0085-3

References

[1]
Allison, V.J., Yermakov, Z., Miller, R.M., Jastrow, J.D., Matamala, R., 2007. Using landscape and depth gradients to decouple the impact of correlated environmental variables on soil microbial community composition. Soil Biology & Biochemistry 39, 505–516
CrossRef Google scholar
[2]
Bais, H.P., Weir, T.L., Perry, L.G., Gilroy, S., Vivanco, J.M., 2006. The role of root exudates in rhizosphere interactions with plants and other organisms. Annual Review of Plant Biology 57, 233–266
CrossRef Google scholar
[3]
Bardgett, R.D., Bowman, W.D., Kaufmann, R., Schmidt, S.K., 2005. A temporal approach to linking aboveground and belowground ecology. Trends in Ecology & Evolution 20, 634–641
CrossRef Google scholar
[4]
Bardgett, R.D., Mommer, L., de Vries, F.T., 2014. Going underground: root traits as drivers of ecosystem processes. Trends in Ecology & Evolution 29, 692–699
CrossRef Google scholar
[5]
Barker, K.R., 1985. Nematode extraction and bioassays, in: Barker, K.R., Carter, C.C., Sasser, J.N., eds., An advanced treatise on Meloidogyne. vol. 2. North Carolina State University Graphics, Raleigh, pp. 19–35. Methodology.
[6]
Bastow, J.L., 2011. Facilitation and predation structure a grassland detrital food web: the responses of soil nematodes to isopod processing of litter. Journal of Animal Ecology 80, 947–957
CrossRef Google scholar
[7]
Bongers, T., 1990. The maturity index: an ecological measure of environmental disturbance based on nematode species composition. Oecologia 83, 14–19
CrossRef Google scholar
[8]
Bongers, T., Ferris, H., 1999. Nematode community structure as a bioindicator in environmental monitoring. Trends in Ecology & Evolution 14, 224–228
CrossRef Google scholar
[9]
Briar, S.S., Culman, S.W., Young-Mathews, A., Jackson, L.E., Ferris, H., 2012. Nematode community responses to a moisture gradient and grazing along a restored riparian corridor. European Journal of Soil Biology 50, 32–38
CrossRef Google scholar
[10]
Chen, H., Dai, Z., Veach, A.M., Zheng, J., Xu, J., Schadt, C.W., 2020b. Global meta-analyses show that conservation tillage practices promote soil fungal and bacterial biomass. Agriculture, Ecosystems & Environment 293, 106841
CrossRef Google scholar
[11]
Chen, Y., Cao, J., He, X., Liu, T., Shao, Y., Zhang, C., Zhou, Q., Li, F., Mao, P., Tao, L., Liu, Z., Lin, Y., Zhou, L., Zhang, W., Fu, S., 2020a. Plant leaf litter plays a more important role than roots in maintaining earthworm communities in subtropical plantations. Soil Biology & Biochemistry 144, 107777
CrossRef Google scholar
[12]
Chen, Y., Zhang, Y., Cao, J., Fu, S., Hu, S., Wu, J., Zhao, J., Liu, Z., 2019. Stand age and species traits alter the effects of understory removal on litter decomposition and nutrient dynamics in subtropical Eucalyptus plantations. Global Ecology and Conservation 20, e00693
CrossRef Google scholar
[13]
De Long, J.R., Laudon, H., Blume-Werry, G., Kardol, P., 2016. Nematode community resistant to deep soil frost in boreal forest soils. Pedobiologia 59, 243–251
CrossRef Google scholar
[14]
Eilers, K.G., Debenport, S., Anderson, S., Fierer, N., 2012. Digging deeper to find unique microbial communities: the strong effect of depth on the structure of bacterial and archaeal communities in soil. Soil Biology & Biochemistry 50, 58–65
CrossRef Google scholar
[15]
Eisenhauer, N., Ferlian, O., Craven, D., Hines, J., Jochum, M., 2019. Ecosystem responses to exotic earthworm invasion in northern North American forests. Research Ideas and Outcomes 5, e34564
CrossRef Google scholar
[16]
Eisenhauer, N., Lanoue, A., Strecker, T., Scheu, S., Steinauer, K., Thakur, M.P., Mommer, L., 2017. Root biomass and exudates link plant diversity with soil bacterial and fungal biomass. Scientific Reports 7, 44641
CrossRef Google scholar
[17]
Eisenhauer, N., Migunova, V.D., Ackermann, M., Ruess, L., Scheu, S., 2011. Changes in plant species richness induce functional shifts in soil nematode communities in experimental grassland. PLoS One 6, e24087
CrossRef Google scholar
[18]
Eisenhauer, N., Reich, P.B., 2012. Above- and below-ground plant inputs both fuel soil food webs. Soil Biology & Biochemistry 45, 156–160
CrossRef Google scholar
[19]
Elfstrand, S., Lagerlöf, J., Hedlund, K., Mårtensson, A., 2008. Carbon routes from decomposing plant residues and living roots into soil food webs assessed with 13C labelling. Soil Biology & Biochemistry 40, 2530–2539
CrossRef Google scholar
[20]
Ferris, H., Bongers, T., de Goede, R.G.M., 2001. A framework for soil food web diagnostics: extension of the nematode faunal analysis concept. Applied Soil Ecology 18, 13–29
CrossRef Google scholar
[21]
Freschet, G.T., Cornwell, W.K., Wardle, D.A., Elumeeva, T.G., Liu, W., Jackson, B.G., Onipchenko, V.G., Soudzilovskaia, N.A., Tao, J., Cornelissen, J.H.C., 2013. Linking litter decomposition of above- and below-ground organs to plant-soil feedbacks worldwide. Journal of Ecology 101, 943–952
CrossRef Google scholar
[22]
Glavatska, O., Müller, K., Butenschoen, O., Schmalwasser, A., Kandeler, E., Scheu, S., Totsche, K.U., Ruess, L., 2017. Disentangling the root- and detritus-based food chain in the micro-food web of an arable soil by plant removal. PLoS One 12, e0180264
CrossRef Google scholar
[23]
Gransee, A., Wittenmayer, L., 2000. Qualitative and quantitative analysis of water soluble root exudates in relation to plant species and development. Journal of Plant Nutrition and Soil Science 163, 381–385
CrossRef Google scholar
[24]
Hsiao, C.J., Sassenrath, G.F., Zeglin, L.H., Hettiarachchi, G.M., Rice, C.W., 2018. Vertical changes of soil microbial properties in claypan soils. Soil Biology & Biochemistry 121, 154–164
CrossRef Google scholar
[25]
Jones, D.L., Kemmitt, S.J., Wright, D., Cuttle, S.P., Bol, R., Edwards, A.C., 2005. Rapid intrinsic rates of amino acid biodegradation in soils are unaffected by agricultural management strategy. Soil Biology & Biochemistry 37, 1267–1275
CrossRef Google scholar
[26]
Kalinkat, G., Brose, U., Rall, B.C., 2013. Habitat structure alters top-down control in litter communities. Oecologia 172, 877–887
CrossRef Google scholar
[27]
Kaneda, S., Kaneko, N., 2011. Influence of Collembola on nitrogen mineralization varies with soil moisture content. Soil Science and Plant Nutrition 57, 40–49
CrossRef Google scholar
[28]
Keith, A.M., Brooker, R.W., Osler, G.H.R., Chapman, S.J., Burslem, D.F.R.P., van der Wal, R., 2009. Strong impacts of belowground tree inputs on soil nematode trophic composition. Soil Biology & Biochemistry 41, 1060–1065
CrossRef Google scholar
[29]
Kudrin, A.A., 2017. Effects of low quantities of added labile carbon on soil nematodes in intact forest soil microcosms. European Journal of Soil Biology 78, 29–37
CrossRef Google scholar
[30]
Lazarova, S.S., de Goede, R.G.M., Peneva, V.K., Bongers, T., 2004. Spatial patterns of variation in the composition and structure of nematode communities in relation to different microhabitats: a case study of Quercus dalechampii Ten. forest. Soil Biology & Biochemistry 36, 701–712
CrossRef Google scholar
[31]
Liu, J., Chen, Y., Du, C., Liu, X., Ma, Q., Zhang, X., Wang, D., 2019. Interactive effects of nitrogen addition and litter on soil nematodes in grassland. European Journal of Soil Science 70, 697–706
CrossRef Google scholar
[32]
Malik, A.A., Chowdhury, S., Schlager, V., Oliver, A., Puissant, J., Vazquez, P.G.M., Jehmlich, N., von Bergen, M., Griffiths, R.I., Gleixner, G., 2016. Soil fungal:bacterial ratios are linked to altered carbon cycling. Frontiers in Microbiology 7, 1247
CrossRef Google scholar
[33]
Moore, J.C., Berlow, E.L., Coleman, D.C., de Ruiter, P.C., Dong, Q., Hastings, A., Johnson, N.C., McCann, K.S., Melville, K., Morin, P.J., Nadelhoffer, K., Rosemond, A.D., Post, D.M., Sabo, J.L., Scow, K.M., Vanni, M.J., Wall, D.H., 2004. Detritus, trophic dynamics and biodiversity. Ecology Letters 7, 584–600
CrossRef Google scholar
[34]
Moradi, J., John, K., Vicentini, F., Veselá, H., Vicena, J., Ardestani, M.M., Frouz, J., 2020. Vertical distribution of soil fauna and microbial community under two contrasting post mining chronosequences: Sites reclaimed by alder plantation and unreclaimed regrowth. Global Ecology and Conservation 23, e01165
CrossRef Google scholar
[35]
Neher, D.A., Darby, B.J., 2009. General community indices that can be used for analysis of nematode assemblages, In: Wilson, M.J., Kakouli-Duarte, T., eds., Nematodes as Environmental Indicators. CABI, Wallingford, pp. 107–123.
[36]
Pausch, J., Hünninghaus, M., Kramer, S., Scharroba, A., Scheunemann, N., Butenschoen, O., Marhan, S., Bonkowski, M., Kandeler, E., Scheu, S., Kuzyakov, Y., Ruess, L., 2018. Carbon budgets of top- and subsoil food webs in an arable system. Pedobiologia 69, 29–33
CrossRef Google scholar
[37]
Pollierer, M.M., Langel, R., Körner, C., Maraun, M., Scheu, S., 2007. The underestimated importance of belowground carbon input for forest soil animal food webs. Ecology Letters 10, 729–736
CrossRef Google scholar
[38]
Potapov, A.M., Goncharov, A.A., Semenina, E.E., Korotkevich, A.Y., Tsurikov, S.M., Rozanova, O.L., Anichkin, A.E., Zuev, A.G., Samoylova, E.S., Semenyuk, I.I., Yevdokimov, I.V., Tiunov, A.V., 2017. Arthropods in the subsoil: Abundance and vertical distribution as related to soil organic matter, microbial biomass and plant roots. European Journal of Soil Biology 82, 88–97
CrossRef Google scholar
[39]
Rooney, N., McCann, K., Gellner, G., Moore, J.C., 2006. Structural asymmetry and the stability of diverse food webs. Nature 442, 265–269
CrossRef Google scholar
[40]
Ruess, L., Ferris, H., 2004. Decomposition pathways and successional changes. Nematology Monographs & Perspectives 2, 547–556.
[41]
Ruf, A., Kuzyakov, Y., Lopatovskaya, O., 2006. Carbon fluxes in soil food webs of increasing complexity revealed by 14C labelling and 13C natural abundance. Soil Biology & Biochemistry 38, 2390–2400
CrossRef Google scholar
[42]
Saj, S., Mikola, J., Ekelund, F., 2009. Species-specific effects of live roots and shoot litter on soil decomposer abundances do not forecast plant litter-nitrogen uptake. Oecologia 161, 331–341
CrossRef Google scholar
[43]
Sauvadet, M., Chauvat, M., Cluzeau, D., Maron, P.A., Villenave, C., Bertrand, I., 2016. The dynamics of soil micro-food web structure and functions vary according to litter quality. Soil Biology & Biochemistry 95, 262–274
CrossRef Google scholar
[44]
Sayer, E.J., 2006. Using experimental manipulation to assess the roles of leaf litter in the functioning of forest ecosystems. Biological Reviews of the Cambridge Philosophical Society 81, 1–31
CrossRef Google scholar
[45]
Scharroba, A., Kramer, S., Kandeler, E., Ruess, L., 2016. Spatial and temporal variation of resource allocation in an arable soil drives community structure and biomass of nematodes and their role in the micro-food web. Pedobiologia 59, 111–120
CrossRef Google scholar
[46]
Shao, Y., Zhang, W., Eisenhauer, N., Liu, T., Xiong, Y., Liang, C., Fu, S., 2017. Nitrogen deposition cancels out exotic earthworm effects on plant-feeding nematode communities. Journal of Animal Ecology 86, 708–717
CrossRef Google scholar
[47]
Sradnick, A., Oltmanns, M., Raupp, J., Joergensen, R.G., 2014. Microbial residue indices down the soil profile after long-term addition of farmyard manure and mineral fertilizer to a sandy soil. Geoderma 226–227, 79–84
CrossRef Google scholar
[48]
Stone, M.M., DeForest, J.L., Plante, A.F., 2014. Changes in extracellular enzyme activity and microbial community structure with soil depth at the Luquillo Critical Zone Observatory. Soil Biology & Biochemistry 75, 237–247
CrossRef Google scholar
[49]
Sun, T., Wang, Y., Hui, D., Jing, X., Feng, W., 2020b. Soil properties rather than climate and ecosystem type control the vertical variations of soil organic carbon, microbial carbon, and microbial quotient. Soil Biology & Biochemistry 148, 107905
CrossRef Google scholar
[50]
Sun, Y., Chen, H.Y.H., Jin, L., Wang, C., Zhang, R., Ruan, H., Yang, J., 2020a. Drought stress induced increase of fungi:bacteria ratio in a poplar plantation. Catena 193, 104607
CrossRef Google scholar
[51]
Tian, Q., Wang, X., Wang, D., Wang, M., Liao, C., Yang, X., Liu, F., 2017. Decoupled linkage between soil carbon and nitrogen mineralization among soil depths in a subtropical mixed forest. Soil Biology & Biochemistry 109, 135–144
CrossRef Google scholar
[52]
Wan, S., Zhang, C., Chen, Y., Zhao, J., Zhu, X., Wu, J., Zhou, L., Lin, Y., Liu, Z., Fu, S., 2015. Interactive effects of understory removal and fertilization on soil respiration in subtropical Eucalyptus plantations. Journal of Plant Ecology 8, 284–290
CrossRef Google scholar
[53]
Wang, Q., He, T., Wang, S., Liu, L., 2013. Carbon input manipulation affects soil respiration and microbial community composition in a subtropical coniferous forest. Agricultural and Forest Meteorology 178–179, 152–160
CrossRef Google scholar
[54]
Yang, L., Liu, N., Ren, H., Wang, J., 2009. Facilitation by two exotic Acacia: Acacia auriculiformis and Acacia mangium as nurse plants in South China. Forest Ecology and Management 257, 1786–1793
CrossRef Google scholar
[55]
Zhang, P., Li, B., Wu, J., Hu, S., 2019. Invasive plants differentially affect soil biota through litter and rhizosphere pathways: a meta-analysis. Ecology Letters 22, 200–210
CrossRef Google scholar
[56]
Zhang, P., Neher, D.A., Li, B., Wu, J., 2018. The impacts of above- and belowground plant input on soil microbiota: invasive Spartina alterniflora versus native Phragmites australis. Ecosystems (New York, N.Y.) 21, 469–481
CrossRef Google scholar
[57]
Zhang, X., Dong, X., Liang, W., 2010. Spatial distribution of soil nematode communities in stable and active sand dunes of Horqin sandy land. Arid Land Research and Management 24, 68–80
CrossRef Google scholar
[58]
Zhao, C., Guo, E., Shao, Y., Zhang, W., Zhang, C., Liu, Y., Li, Y., Zou, X., Fu, S., 2021. Impacts of litter addition and root presence on soil nematode community structure in a young Eucalyptus plantation in southern China. Forest Ecology and Management 479, 118633
CrossRef Google scholar
[59]
Zhao, C., Miao, Y., Yu, C., Zhu, L., Wang, F., Jiang, L., Hui, D., Wan, S., 2015b. Soil microbial community composition and respiration along an experimental precipitation gradient in a semiarid steppe. Scientific Reports 6, 24317
CrossRef Google scholar
[60]
Zhao, C., Sun, F., Yu, C., Zhu, L., Li, Y., Zhou, Z., Yang, G., Wang, W., Miao, R., 2018. Soil nematode trophic groups in four different plantations in southern China: implications for restoration. Polish Journal of Environmental Studies 27, 1379–1386
CrossRef Google scholar
[61]
Zhao, C., Zhao, J., Wu, J., Classen, A.T., Li, Y., Lou, Y., Zhang, W., Jing, X., Shao, Y., Fu, S., 2019. Bamboo forest management leads to a shift in the soil energy channel. Geoderma 353, 201–203
CrossRef Google scholar
[62]
Zhao, J., Li, D., Fu, S., He, X., Fu, Z., Zhang, W., Wang, K., 2016. Using the biomasses of soil nematode taxa as weighting factors for assessing soil food web conditions. Ecological Indicators 60, 310–316
CrossRef Google scholar
[63]
Zhao, J., Zhao, C., Wan, S., Wang, X., Zhou, L., Fu, S., 2015a. Soil nematode assemblages in an acid soil as affected by lime application. Nematology 17, 179–191
CrossRef Google scholar

Acknowledgments

This study was supported by the NSFC-Henan Joint Fund (U1804101, U1904204), Henan Key Scientific and Technological Project (192102110160), the National Natural Science Foundation of China (31800405), Innovation Scientists and Technicians Troop Construction Projects of Henan Province.

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