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Herbivore Dung Promotes Plant Litter Decomposition Rate in a Semi-arid Grassland Ecosystem

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The decomposition of plant litter and animal dung is the key processes of nutrient cycling and has been studied in a wide range of grassland ecosystems. However, most studies focus on the separate processes of either plant litter or animal dung decomposition, while the interactions between these two processes, which occur in grazed grassland ecosystems, are rarely studied. We conducted an experiment in a semi-arid grassland in Central Inner Mongolia, to examine the mass loss rates and chemical composition changes of two plant litter species and three herbivore dung types separately or in combination over a 2-year period. Twenty litterbag treatments were used to represent 2 treatments of plant litter only, 6 treatments of herbivore dung only at two addition levels, and 12 treatments of litter and dung combinations. We found that horse dung had the biggest mass loss rate, followed by cattle dung and sheep dung, either separately or mixed with plant litter. Dung addition promoted the mass loss, nitrogen release and fiber fraction (hemicellulose, cellulose and lignin) loss of plant litter, and the promotion was strongest for cattle dung, weakest for sheep dung, and stronger at high dung addition levels and in the early stages. However, the effect of litter addition on dung decomposition, a negative effect, was significant only when the dung proportion was low in the litter and dung mixture (that is, in the treatment of 10 g litter + 6 g dung). Furthermore, a significant positive non-additive effect of mixing litter and dung on their total mass loss was detected for the mixture at a litter:dung ratio of 10:6, the ratio in the major grazing area of the grassland. Our findings suggest that mixture of herbivore dung with plant litter, as in actual grassland ecosystems, promotes litter decomposition, and the composition of the litter and dung in mixture, though it may inhibit dung decomposition, due to the changes in chemical stoichiometry of decomposing materials and biophysical microenvironment by the mixing. It is necessary to incorporate the non-additive effect of litter and dung mixture in modeling carbon and nutrient cycling of grassland ecosystems.

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References

  • Bardgett RD, Keiller S, Cook R, Gilburn AS. 1998. Dynamic interactions between soil animals and microorganisms in upland grassland soils amended with sheep dung: a microcosm experiment. Soil Biology and Biochemistry 30:531–539.

    Article  CAS  Google Scholar 

  • Berg B, Mcclaugherty C. 2013. Plant litter: decomposition humus formation carbon sequestration, 3rd edn. Springer press.

    Google Scholar 

  • Berglund SL, Agren GI, Ekblad A. 2013. Carbon and nitrogen transfer in leaf litter mixtures. Soil Biology and Biochemistry 57:341–348.

    Article  CAS  Google Scholar 

  • Bloor JMG. 2015. Additive effects of dung amendment and plant species identity on soil processes and soil inorganic nitrogen in grass monocultures. Plant and Soil 396:189–200.

    Article  CAS  Google Scholar 

  • Briones MJI, Ineson P. 1996. Decomposition of eucalyptus leaves in litter mixtures. Soil Biology and Biochemistry 28:1381–1388.

    Article  CAS  Google Scholar 

  • Cai Y, Wang X, Tian L, Zhao H, Lu X, Yan YJSB, Biochemistry. 2014. The impact of excretal returns from yak and Tibetan sheep dung on nitrous oxide emissions in an alpine steppe on the Qinghai-Tibetan Plateau. Soil Biology and Biochemistry 76:90–99.

    Article  CAS  Google Scholar 

  • Chao L, Liu YY, Freschet GT, Zhang WD, Yu X, Zheng WH, Guan X, Yang QP, Chen LC, Dijkstra FA, Wang SL. 2019. Litter carbon and nutrient chemistry control the magnitude of soil priming effect. Functional Ecology 33:876–888.

    Article  Google Scholar 

  • Cornwell WK, Cornelissen JH, Amatangelo K, Dorrepaal E, Eviner VT, Godoy O, Hobbie SE, Hoorens B, Kurokawa H, Pérez-Harguindeguy N. 2008. Plant species traits are the predominant control on litter decomposition rates within biomes worldwide. Ecology Letters 11:1065–1071.

    Article  PubMed  Google Scholar 

  • Delgado-Baquerizo M, García-Palacios P, Milla R, Gallardo A, Maestre FT. 2015. Soil characteristics determine soil carbon and nitrogen availability during leaf litter decomposition regardless of litter quality. Soil Biology and Biochemistry 81:134–142.

    Article  CAS  Google Scholar 

  • Du Z, Wang X, Xiang J, Wu Y, Zhang B, Yan Y, Zhang X, Cai Y. 2021. Yak dung pat fragmentation affects its carbon and nitrogen leaching in Northern Tibet, China. Agriculture, Ecosystems and Environment 310:107301.

    Article  CAS  Google Scholar 

  • Eriksson KE, Blanchette RA, Ander P. 1990. Springer series in wood science microbial and enzymatic degradation of wood and wood components. Berlin: Springer Verlag press.

    Book  Google Scholar 

  • Frey SD, Knorr M, Parrent JL, Simpson RT. 2004. Chronic nitrogen enrichment affects the structure and function of the soil microbial community in temperate hardwood and pine forests. Forest Ecology and Management 196:159–171.

    Article  Google Scholar 

  • Haynes R, Williams P. 1993. Nutrient cycling and soil fertility in the grazed pasture ecosystem. Elsevier press. p119–199.

  • Kohn RA, Dinneen MM, Russek-Cohen E. 2005. Using blood urea nitrogen to predict nitrogen excretion and efficiency of nitrogen utilization in cattle, sheep, goats, horses, pigs, and rats. Journal of Animal Science 83:879–889.

    Article  CAS  PubMed  Google Scholar 

  • Li F, Wang Y, Guo K, Wesche K. 2019. Grasslands of China. USA: Elsevier press.

    Google Scholar 

  • Liang DF, Niu KC, Zhang ST. 2017. Interacting effects of yak dung deposition and litter quality on litter mass loss and nitrogen dynamics in Tibetan alpine grassland. Grass and Forage Science 73:123–131.

    Article  Google Scholar 

  • Liao W, Wen ZY, Hurley S, Liu Y, Liu CB, Chen SL. 2005. Effects of hemicellulose and lignin on enzymatic hydrolysis of cellulose from dairy manure. Applied Biochemistry and Biotechnology 121:1017–1030.

    Article  PubMed  Google Scholar 

  • Liu J, Liu X, Song Q, Compson ZG, LeRoy CJ, Luan F, Wang H, Hu Y, Yang Q. 2020. Synergistic effects: a common theme in mixed-species litter decomposition. New Phytologist 277:757–765.

    Article  Google Scholar 

  • Makkonen M, Berg MP, van Logtestijn RSP, van Hal JR, Aerts R. 2013. Do physical plant litter traits explain non-additivity in litter mixtures? A test of the improved microenvironmental conditions theory. Oikos 122:987–997.

    Article  Google Scholar 

  • Markewich HA, Pell AN, Mbugua DM, Cherney DJR, van Es HM, Lehmann J, Robertson JB. 2010. Effects of storage methods on chemical composition of manure and manure decomposition in soil in small-scale Kenyan systems. Agriculture Ecosystems and Environment 139:134–141.

    Article  Google Scholar 

  • Martinez-Garcia LB, Korthals GW, Brussaard L, Mainardi G, De Deyn GB. 2021. Litter quality drives nitrogen release, and agricultural management (organic vs. conventional) drives carbon loss during litter decomposition in agro-ecosystems. Soil Biology and Biochemistry 153:9.

    Article  Google Scholar 

  • Mora-Gómez J, Elosegi A, Duarte S, Cássio F, Pascoal C, Romaní AM. 2016. Differences in the sensitivity of fungi and bacteria to season and invertebrates affect leaf litter decomposition in a Mediterranean stream. FEMS Microbiology Ecology 92:121.

    Article  Google Scholar 

  • Moro MJ, Domingo F. 2000. Litter decomposition in four woody species in a mediterranean climate: Weight loss, N and P dynamics. Annals of Botany 86:1065–1071.

    Article  CAS  Google Scholar 

  • Mroczunski R, Komosinski K. 2014. Differences between beetle communities colonizing cattle and horse dung. European Journal of Entomology 111:349–355.

    Article  Google Scholar 

  • Nichols E, Spector S, Louzada J, Larsen T, Amequita S, Favila ME, Scarabaeinae Res N. 2008. Ecological functions and ecosystem services provided by Scarabaeinae dung beetles. Biological Conservation 141:1461–1474.

    Article  Google Scholar 

  • Nichols KL, Del Grosso SJ, Derner JD, Follett RF, Archibeque SL, Stewart CE, Paustian KH. 2016. Nitrous oxide and methane fluxes from cattle excrement on C3 pasture and C4-dominated shortgrass steppe. Agriculture Ecosystems and Environment 225:104–115.

    Article  CAS  Google Scholar 

  • Olson JS. 1963. Energy storage and the balance of producers and decomposers in ecological systems. Ecology 44:322–331.

    Article  Google Scholar 

  • Ross LC, Woodin SJ, Hester AJ, Thompson DB, Birks HJB. 2012. Biotic homogenization of upland vegetation: patterns and drivers at multiple spatial scales over five decades. Journal of Vegetation Science 23:755–770.

    Article  Google Scholar 

  • Seastedt T. 1984. The Role of Microarthropods in Decomposition and Mineralization Processes. Annual Review of Entomology 29:25–46.

    Article  Google Scholar 

  • Sitters J, Maechler MJ, Edwards PJ, Suter W, Venterink HO. 2014. Interactions between C:N: P stoichiometry and soil macrofauna control dung decomposition of savanna herbivores. Functional Ecology 28:776–786.

    Article  Google Scholar 

  • Somda ZC, Powell JM. 1998. Seasonal decomposition of sheep manure and forage leaves in soil. Communications in Soil Science and Plant Analysis 29:2961–2979.

    Article  CAS  Google Scholar 

  • Sun Y, He XZ, Hou FJ, Wang ZF, Chang SH. 2018. Grazing increases litter decomposition rate but decreases nitrogen release rate in an alpine meadow. Biogeosciences 15:4233–4243.

    Article  CAS  Google Scholar 

  • Swift MJ, Heal OW, Anderson JM, Anderson J. 1979. Decomposition in terrestrial ecosystems: Univ of California Press.

  • Trofymow J, Moore T, Titus B, Prescott C, Morrison I, Siltanen M, Smith S, Fyles J, Wein R, Camiré C. 2002. Rates of litter decomposition over 6 years in Canadian forests: influence of litter quality and climate. Canadian Journal of Forest Research 32(5):789–804.

    Article  Google Scholar 

  • Uselman SM, Snyder KA, Blank RR, Jones TJ. 2011. UVB exposure does not accelerate rates of litter decomposition in a semi-arid riparian ecosystem. Soil Biology and Biochemistry 43:1254–1265.

    Article  CAS  Google Scholar 

  • Vos VCA, van Ruijven J, Berg MP, Peeters E, Berendse F. 2011. Macro-detritivore identity drives leaf litter diversity effects. Oikos 120:1092–1098.

    Article  Google Scholar 

  • Vossbrinck CR, Coleman DC, Woolley TA. 1979. Abiotic and biotic factors in litter decomposition in a semi-arid grassland. Ecology 60:265–271.

    Article  CAS  Google Scholar 

  • Wang JZ, Wang DL, Li CQ, Seastedt TR, Liang CZ, Wang L, Sun W, Liang MW, Li Y. 2018. Feces nitrogen release induced by different large herbivores in a dry grassland. Ecological Applications 28:201–211.

    Article  PubMed  Google Scholar 

  • Wang YN, Li FY, Song X, Wang XS, Suri G, Baoyin T. 2020. Changes in litter decomposition rate of dominant plants in a semi-arid steppe across different land-use types: Soil moisture, not home-field advantage, plays a dominant role. Agriculture, Ecosystems and Environment 303:107119.

    Article  CAS  Google Scholar 

  • Wang ZY, Liu ZY, Baoyin T, Jimoh SO, Zhang TR, Cheng JW, Li FYH. 2021. Assessing the burning of household dung-cake as an energy source in different rangeland regions of Inner Mongolia. Journal of Cleaner Production 292:125827. https://doi.org/10.1016/j.jclepro.2021.125827.

    Article  Google Scholar 

  • Wardle DA, Bonner KI, Nicholson KS. 1997. Biodiversity and plant litter: Experimental evidence which does not support the view that enhanced species richness improves ecosystem function. Oikos 79:247–258.

    Article  Google Scholar 

  • Wardle DA, Bardgett RD, Klironomos JN, Setälä H, Van Der Putten WH, Wall DH. 2004. Ecological linkages between aboveground and belowground biota. Science 304:1629–1633.

    Article  CAS  PubMed  Google Scholar 

  • Wu GL, Zhang MQ, Liu Y, Lopez-Vicente M. 2020. Litter cover promotes biocrust decomposition and surface soil functions in sandy ecosystem. Geoderma 374:114429.

    Article  CAS  Google Scholar 

  • Yang C, Zhang Y, Hou F, Millner JP, Wang Z, Chang S. 2019a. Grazing activity increases decomposition of yak dung and litter in an alpine meadow on the Qinghai-Tibet plateau. Plant and Soil 444:239–250.

    Article  CAS  Google Scholar 

  • Yang J, Wang YF, Cui XY, Zhang YM, Yu ZS. 2019b. Do different livestock dwellings on single grassland share similar faecal microbial communities? Applied Microbiology and Biotechnology 103:5023–5037.

    Article  CAS  PubMed  Google Scholar 

  • Yoshitake S, Soutome H, Koizumi H. 2014. Deposition and decomposition of cattle dung and its impact on soil properties and plant growth in a cool-temperate pasture. Ecological Research 29:673–684.

    Article  Google Scholar 

  • Zhang D, Hui D, Luo Y, Zhou G. 2008. Rates of litter decomposition in terrestrial ecosystems: global patterns and controlling factors. Journal of Plant Ecology 1:85–93.

    Article  Google Scholar 

  • Zhou SX, Butenschoen O, Barantal S, Handa IT, Makkonen M, Vos V, Aerts R, Berg MP, McKie B, Van Ruijven J, Hattenschwiler S, Scheu S. 2020. Decomposition of leaf litter mixtures across biomes: the role of litter identity, diversity and soil fauna. Journal of Ecology 108:2283–2297.

    Article  Google Scholar 

  • Zhu YH, Merbold L, Pelster D, Diaz-Pines E, Wanyama GN, Butterbach-Bahl K. 2018. Effect of dung quantity and quality on greenhouse gas fluxes from tropical pastures in Kenya. Global Biogeochemical Cycles 32:1589–1604.

    Article  CAS  Google Scholar 

  • Zhu YH, Merhold L, Lehner S, Pelster DE, Okoma SA, Ngetich F, Onyango AA, Pellikka P, Butterbach-Bahl K. 2020. The effects of climate on decomposition of cattle, sheep and goat manure in Kenyan tropical pastures. Plant and Soil 451:325–343.

    Article  CAS  Google Scholar 

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Funding

The research was supported by the National Natural Science Foundation of China (Grant No. 32071564), and the Department of Science and Technology (Grant No. 2019ZD007, and Grant for Key Basic Research Project on Grassland Ecosystems) and Department of Finance of the Inner Mongolia Autonomous Region of China.

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Correspondence to FrankYonghong Li.

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Wang, Y., Li, F., Liu, Y. et al. Herbivore Dung Promotes Plant Litter Decomposition Rate in a Semi-arid Grassland Ecosystem. Ecosystems 26, 661–674 (2023). https://doi.org/10.1007/s10021-022-00784-3

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