Please wait a minute...
Journal of Arid Land  2014, Vol. 6 Issue (4): 432-444    DOI: 10.1007/s40333-014-0002-z
Research Articles     
Litter decomposition and C and N dynamics as affected by N additions in a semi-arid temperate steppe, Inner Mongolia of China
Qin PENG1, YuChun QI1, YunShe DONG1, YaTing HE1,2, ShengSheng XIAO3, XinChao LIU1,2, LiangJie SUN1,2, JunQiang JIA1,2, ShuFang GUO1,2, CongCong CAO1,2
1 Institute of Geographic Sciences and Natural Resources Research, Chinese Academy of Sciences, Beijing 100101, China;
2 University of Chinese Academy of Sciences, Beijing 100049, China;
3 Jiangxi Provincial Research Institute for Soil and Water Conservation, Nanchang 330029, China
Download:   PDF(322KB)
Export: BibTeX | EndNote (RIS)      

Abstract   Litter decomposition is the fundamental process in nutrient cycling and soil carbon (C) sequestration in terrestrial ecosystems. The global-wide increase in nitrogen (N) inputs is expected to alter litter decomposition and,ultimately, affect ecosystem C storage and nutrient status. Temperate grassland ecosystems in China are usually N-deficient and particularly sensitive to the changes in exogenous N additions. In this paper, we conducted a 1,200-day in situ experiment in a typical semi-arid temperate steppe in Inner Mongolia to investigate the litter decomposition as well as the dynamics of litter C and N concentrations under three N addition levels (low N with 50 kg N/(hm2•a) (LN), medium N with 100 kg N/(hm2•a) (MN), and high N with 200 kg N/(hm2•a) (HN)) and three N addition forms (ammonium-N-based with 100 kg N/(hm2•a) as ammonium sulfate (AS), nitrate-N-based with 100 kg N/(hm2•a) as sodium nitrate (SN), and mixed-N-based with 100 kg N/(hm2•a) as calcium ammonium nitrate (CAN)) compared to control with no N addition (CK). The results indicated that the litter mass remaining in all N treatments exhib¬ited a similar decomposition pattern: fast decomposition within the initial 120 days, followed by a relatively slow decomposition in the remaining observation period (120–1,200 days). The decomposition pattern in each treatment was fitted well in two split-phase models, namely, a single exponential decay model in phase I (<398 days) and a linear decay function in phase II (>398 days). The three N addition levels exerted insignificant effects on litter decomposition in the early stages (<398 days, phase I; P>0.05). However, MN and HN treatments inhibited litter mass loss after 398 and 746 days, respectively (P<0.05). AS and SN treatments exerted similar effects on litter mass remaining during the entire decomposition period (P>0.05). The effects of these two N addition forms differed greatly from those of CAN after 746 and 1,053 days, respectively (P<0.05). During the decomposition period, N concentrations in the decomposing litter increased whereas C concentrations decreased, which also led to an exponential decrease in litter C:N ratios in all treatments. No significant effects were induced by N addition levels and forms on litter C and N concentrations (P>0.05). Our results indicated that exogenous N additions could exhibit neutral or inhibitory effects on litter decomposition, and the inhibitory effects of N additions on litter decomposition in the final decay stages are not caused by the changes in the chemical qualities of the litter, such as endogenous N and C concentrations. These results will provide an important data basis for the simulation and prediction of C cycle processes in future N-deposition scenarios.

Key wordsbiomass allocation      drought      temperature      persistence time      semi-arid area     
Received: 27 June 2013      Published: 12 August 2014
Fund:  

The National Natural Science Foundation of China (41073061, 41203054, 40730105, 40973057) and the Knowledge Innovation Program of the Chinese Academy of Sciences (KZCX2-EW-302).

Corresponding Authors:
Cite this article:

Qin PENG, YuChun QI, YunShe DONG, YaTing HE, ShengSheng XIAO, XinChao LIU, LiangJie SUN, JunQiang JIA, ShuFang GUO, CongCong CAO. Litter decomposition and C and N dynamics as affected by N additions in a semi-arid temperate steppe, Inner Mongolia of China. Journal of Arid Land, 2014, 6(4): 432-444.

URL:

http://jal.xjegi.com/10.1007/s40333-014-0002-z     OR     http://jal.xjegi.com/Y2014/V6/I4/432

Aber J D, Melillo J M, McClaugherty C A. 1990. Predicting long-term patterns of mass loss, nitrogen dynamics, and soil organic matter formation from initial fine litter chemistry in temperate forest ecosystems. Canadian Journal of Botany, 68: 2201–2208.

Aerts R, van Logtestijn R S P, Karlsson P S. 2006. Nitrogen supply differentially affects litter decomposition rates and nitrogen dynamics of sub-arctic bog species. Oecologia, 146: 652–658.

Ågren G I, Bosatta E. 1996. Quality: A bridge between theory and experiment in soil organic matter studies. Oikos, 76: 522–528.

Ågren G I, Bosatta E, Magill A H. 2001. Combining theory and experiment to understand effects of inorganic nitrogen on litter decomposition. Oecologia, 128: 94–98.

Allison S D, Czimczik C I, Treseder K K. 2008. Microbial activity and soil respiration under nitrogen addition in Alaskan boreal forest. Global Change Biology, 14: 1156–1168.

Allison S D, LeBauer D S, Ofrecio M R, et al. 2009. Low levels of nitrogen addition stimulate decomposition by boreal forest fungi. Soil Biology and Biochemistry, 41: 293–302.

Almagro M, Martínez-Mena M. 2012. Exploring short-term leaf litter decomposition dynamics in a Mediterranean ecosystem: dependence on litter type and site conditions. Plant and Soil, 358: 323–335.

Amundson R. 2001. The carbon budget in soils. Annual Review of Earth and Planetary Sciences, 29: 535–562.

Apolinário V X O, Dubeux J C B, Mello A C L, et al. 2013. Deposition and decomposition of signal grass pasture litter under varying nitrogen fertilizer and stocking rates. Crop Ecology and Physiology, 105: 999–1004.

Axelsson G, Berg B. 1988. Fixation of ammonia (15N) to Pinus sylvestris needle litter in different stages of decomposition. Scandi¬navian Journal of Forest Research, 3: 273–279.

Bardgett R D, Streeter T, Bol R. 2003. Soil microbes compete effectively with plants for organic nitrogen inputs to temperate grasslands. Ecology, 84: 1277–1287.

Berg B. 1986. Nutrient release from litter and humus in coniferous forest soils, a mini review. Scandinavian Journal of Forest Research, 1: 359–370.

Berg B, Tamm C O. 1994. Decomposition and nutrient dynamics of litter in long-term optimum nutrition experiments. II. Nutrient concentrations in decomposing Picea abies needle litter. Scandinavian Journal of Forest Research, 9: 99–105.

Berg B, Laskowski R. 2006. Litter decomposition: a guide to carbon and nutrient turnover. In: Advances in Ecological Research (Vol. 38). Amsterdam: Elsevier Academic Press, 38: 20–71.

Berg B, McClaugherty C. 2008. Plant Litter: Decomposition, Humus Formation, Carbon Sequestration (2nd ed.). Berlin: Springer.

Berg M P, Kniese J P, Zoomer R, et al. 1998. Long-term decomposition of successive organic strata in an N saturated Scots pine forest soil. Forest Ecology and Management, 107: 159–172.

Berglund S L, Ågren G I. 2012. When will litter mixtures decompose faster or slower than individual litters? A model for two litters. Oikos, 121: 1112–1120.

Bosatta E, Staaf H. 1982. The control of nitrogen turnover in forest litter. Oikos, 39: 143–151.

Cao G, Tang Y, Mo W, et al. 2004. Grazing intensity alters soil respiration in an alpine meadow on the Tibetan plateau. Soil Biology and Biochemistry, 36: 237–243.

Chadwick D R, Ineson P, Woods C, et al. 1998. Decomposition of Pinus sylvestris litter in litter bags: influence of underlying native litter layer. Soil Biology and Biochemistry, 30: 47–55.

Chen Z, Wang S. 2000. Typical Steppe Ecosystems of China. Beijing: Science Press.

Cleland E E, Harpole W S. 2010. Nitrogen enrichment and plant communities. Annals of the New York Academy of Sciences, 1195: 46–61.

Conn C E, Day F P. 1996. Response of root and cotton strip decay to nitrogen amendment along a barrier island dune chronosequences. Canadian Journal of Botany, 74: 276–284.

Couteaux M M, Bottner P, Berg B. 1995. Litter decomposition, climate and litter quality. Trends in Ecology and Evolution, 10: 63–66.

Dentener F, Drevet J, Lamarque J F, et al. 2006. Nitrogen and sulfur deposition on regional and global scales: A multimodel evaluation. Global Biogeochemical Cycles, 20, GB4003, doi: 10.1029/2005GB002672.

Dijkstra F A, Hobbie S E, Knops J M H, et al. 2004. Nitrogen deposition and plant species interact to influence soil carbon stabilization. Ecology Letters, 7: 1192–1198.

Edmonds R L. 1980. Litter decomposition and nutrient release in Douglas-fir, red alder, western hemlock, and Pacific silver fir ecosystems in western Washington. Canadian Journal of Forest Research, 10: 327–337.

Fog K. 1988. The effect of added nitrogen on the rate of decomposition of organic-matter. Biological Reviews, 63: 433–462.

Gruber N, Galloway J N. 2008. An earth-system perspective of the global nitrogen cycle. Nature, 451: 293–296.

Hart S C, Firestone M K, Paul E A. 1992. Decomposition and nutrient dynamics of ponderosa pine needles in a Mediterranean-type climate. Canadian Journal of Forest Research, 22: 306–314.

Hart S C. 1999. Nitrogen transformations in fallen tree boles and mineral soil of an old-growth forest. Ecology, 80: 1385–1394.

Hobbie S E. 2000. Interactions between litter lignin and soil nitrogen availability during leaf litter decomposition in a Hawaiian Montane forest. Ecosystems, 3: 484–494.

Hobbie S E. 2008. Nitrogen effects on decomposition: a five-year experiment in eight temperate sites. Ecology, 89: 2633–2644.

Hooper D U, Johnson L. 1999. Nitrogen limitation in dryland ecosystems: responses to geographical and temporal variation in precipitation. Biogeochemistry, 46: 247–293.

Hu L H, Zeng D H, Liu Y X, et al. 2010. Response of soil chemical and biological properties to nitrogen addition in a Dahurian larch plantation in Northeast China. Plant and soil, 333: 81–92.

Jiang Y F, Yin X Q, Wang F B. 2013. The influence of litter mixing on decomposition and soil fauna assemblages in a Pinus koraiensis mixed broad-leaved forest of the Changbai Mountains, China. European Journal of Soil Biology, 55: 28–39.

Kang L, Han X, Zhang Z, et al. 2007. Grassland ecosystems in China: review of current knowledge and research advancement. Philosophical Transactions of the Royal Society, 362: 997–1008.

Knorr M, Frey S D, Curtis P S. 2005. Nitrogen additions and litter decomposition: a meta-analysis. Ecology, 86: 3252–3257.

Kochsiek A E. 2010. Litter carbon dynamics: the importance of decomposition, accretion, and sequestration in understanding ecosystem carbon cycling. PhD Dissertation. Lincoln: University of Nebraska-Lincoln.

LeBauer D S, Treseder K K. 2008. Nitrogen limitation of net primary productivity in terrestrial ecosystems is globally distributed. Ecology, 89: 371–379.

Li L J, Zeng D H, Yu Z Y, et al. 2011. Impact of litter quality and soil nutrient availability on leaf decomposition rate in a semi-arid grassland of Northeast China. Journal of Arid Environments, 75: 787–792.

Liao L P, Gao H, Wang S L, et al. 2000. The effect of nitrogen addition on soil nutrient leaching and the decomposition of Chinese fir leaf litter. Acta Phytoecologica Sinica, 24(1): 34–39.

Liu K, Sollenberger L E, Silveira M L, et al. 2011. Grazing intensity and nitrogen fertilization affect litter responses in "Tifton 85" bermudagrass pastures: II. Decomposition and nutrient mineralization. Agronomy Journal, 103: 163–168.

Liu P, Huang J H, Sun J X, et al. 2010a. Litter decomposition and nutrient release as affected by soil nitrogen availability and litter quality in a semiarid grassland ecosystem. Oecologia, 162: 771–780.

Liu X J, Song L, He C E, et al. 2010b. Nitrogen deposition as an important nutrient from the environment and its impact on ecosystems in China. Journal of Arid Land, 2: 137–143.

Liu X J, Zhang Y, Han W X, et al. 2013. Enhanced nitrogen deposition over China. Nature, 494: 459–462.

Magill A H, Aber J D. 1998. Long-term effects of experimental nitrogen additions on foliar litter decay and humus formation in forest ecosystems. Plant and Soil, 203: 301–311.

Manzoni S, Jackson R B, Trofymow J A, et al. 2008. The global stoichiometry of litter nitrogen mineralization. Science, 321: 684–686.

Manzoni S, Trofymow J A, Jackson R B, et al. 2010. Stoichiometric controls on carbon, nitrogen, and phosphorus dynamics in decomposing litter. Ecological Monographs, 80: 89–106.

McClaugherty C A, Pastor J, Aber J D. 1985. Forest litter decomposition in relation to soil nitrogen dynamics and litter quality. Ecology, 66: 266–275.

Mehta N, Dinakaran J, Patel S, et al. 2013. Changes in litter decomposition and soil organic carbon in a reforested tropical deciduous cover (India). Ecological Research, 28: 239–248.

Mo J M, Brown S, Xue J H, et al. 2006. Response of litter decomposition to simulated nitrogen deposition in disturbed, rehabilitated and mature forests in subtropical China. Plant and Soil, 285: 135–151.

Moore J C, Berlow E L, Coleman D C, et al. 2004. Detritus, trophic dynamics and biodiversity. Ecology Letters, 7: 584–600.

Moore T R, Trofymow J A, Prescott C E, et al. 2006. Patterns of carbon, nitrogen and phosphorus dynamics in decomposing foliar litter in Canadian forests. Ecosystems, 9: 46–62.

Oladoye A O, Ola-Adams B A, Adedire M A, et al. 2008. Nutrient dynamics and litter decomposition in Leucaena leucocephala (Lam.) de wit plantation in the Nigerian derived savanna. West African Journal of Applied Ecology, 13: 96–103.

Parton W, Silver W L, Burke I C, et al. 2007. Global-scale similarities in nitrogen release patterns during long-term decomposition. Science, 315: 361–364.

Peng Q, Dong Y S, Qi Y C, et al. 2011a. Effects of nitrogen fertilization on soil respiration in temperate grassland in Inner Mongolia, China. Environmental Earth Sciences, 62: 1163–1171.

Peng Q, Qi Y C, Dong Y S, et al. 2011b. Soil nitrous oxide emissions from a typical semiarid temperatesteppe in Inner Mongolia: effects of mineral nitrogen fertilizer levels and forms. Plant and soil, 342: 345–357.

Prescott C E. 2005. Do rates of litter decomposition tell usanything we really need to know? Forest Ecology and Management, 220: 66–74.

Rovira P, Vallejo V R. 2000. Examination of thermal and acid hydrolysis proceduresin characterization of soil organic matter. Communications in Soil Science and Plant Analysis, 31: 81–100.

Rovira P, Rovira R. 2010. Fitting litter decomposition datasets to mathematical curves: Towards a generalised exponential approach. Geoderma, 155: 329–343.  

Schadt C W, Martin A P, Lipson D A. 2003. Seasonal dynamics of novel fungal lineages in tundra soils. Science, 301: 1359–1361.

Sinsabaugh R L, Carreiro M M, Repert D A. 2002. Allocation of extracellular enzymatic activity in relation to litter composition, N deposition, and mass loss. Biogeochemistry, 60: 1–24.

Sun H L. 2005. Ecosystems of China. Beijing: Science Press.

Vivanco L, Austin A T. 2011. Nitrogen addition stimulates forest litter decomposition and disrupts species interactions in Patagonia, Argentina. Global Change Biology, 17: 1963–1974.

Waldrop M P, Zak D R, Singsabaugh R L, et al. 2004. Nitrogen deposition modifies soil carbon storage through changes in microbial enzymatic activity. Ecological Applications, 14: 1172–1177.

Wang C, Han G, Jia Y, et al. 2011. Response of litter decomposition and related soilenzyme activities to different forms of nitrogen fertilization in a subtropical forest. Ecological Research, 26: 505–513.

Wardle D A, Nilsson M C, Zackrisson O, et al. 2003. Determinants of litter mixing effects in a Swedish boreal forest. Soil Biology and Biochemistry, 35: 827–835.

Zhang J, Han X. 2008. N2O emission from the semi-arid ecosystem under mineral fertilizer (urea and superphosphate) and increased precipitation in northern China. Atmospheric Environment, 42: 291–302.

Zhang W, Wang S. 2012. Effects of NH4+ and NO3– on litter and soil organic carbon decomposition in a Chinese fir plantation forest in South China. Soil Biology and Biochemistry, 47: 116–122.

Zhang Y, Liu X J, Zhang F S, et al. 2006. Spatial and temporal variation of atmospheric nitrogen deposition in the North China Plain. Acta Ecologica Sinica, 26(6): 1633−1639.

Zhou Q, Liu Q P, Lin Z S. 2006. Effects of global warming on constructive species of Leymus chinensis grassland in Inner Mongolia of China. Chinese Journal of Ecology, 25(1): 24–28.

 
[1] ZHAO Xuqin, LUO Min, MENG Fanhao, SA Chula, BAO Shanhu, BAO Yuhai. Spatiotemporal changes of gross primary productivity and its response to drought in the Mongolian Plateau under climate change[J]. Journal of Arid Land, 2024, 16(1): 46-70.
[2] CHEN Yingying, LIN Yajun, ZHOU Xiaobing, ZHANG Jing, YANG Chunhong, ZHANG Yuanming. Effects of drought treatment on photosystem II activity in the ephemeral plant Erodium oxyrhinchum[J]. Journal of Arid Land, 2023, 15(6): 724-739.
[3] Fateme RIGI, Morteza SABERI, Mahdieh EBRAHIMI. Improved drought tolerance in Festuca ovina L. using plant growth promoting bacteria[J]. Journal of Arid Land, 2023, 15(6): 740-755.
[4] BAI Miao, LI Zhanling, HUO Pengying, WANG Jiawen, LI Zhanjie. Propagation characteristics from meteorological drought to agricultural drought over the Heihe River Basin, Northwest China[J]. Journal of Arid Land, 2023, 15(5): 523-544.
[5] Sakine KOOHI, Hadi RAMEZANI ETEDALI. Future meteorological drought conditions in southwestern Iran based on the NEX-GDDP climate dataset[J]. Journal of Arid Land, 2023, 15(4): 377-392.
[6] Mohammad Hossein TAGHIZADEH, Mohammad FARZAM, Jafar NABATI. Rhizobacteria facilitate physiological and biochemical drought tolerance of Halimodendron halodendron (Pall.) Voss[J]. Journal of Arid Land, 2023, 15(2): 205-217.
[7] ZHAO Lili, LI Lusheng, LI Yanbin, ZHONG Huayu, ZHANG Fang, ZHU Junzhen, DING Yibo. Monitoring vegetation drought in the nine major river basins of China based on a new developed Vegetation Drought Condition Index[J]. Journal of Arid Land, 2023, 15(12): 1421-1438.
[8] Mahdi SEDIGHKIA, Bithin DATTA. Analyzing environmental flow supply in the semi-arid area through integrating drought analysis and optimal operation of reservoir[J]. Journal of Arid Land, 2023, 15(12): 1439-1454.
[9] Olfa TERWAYET BAYOULI, ZHANG Wanchang, Houssem TERWAYET BAYOULI. Combining RUSLE model and the vegetation health index to unravel the relationship between soil erosion and droughts in southeastern Tunisia[J]. Journal of Arid Land, 2023, 15(11): 1269-1289.
[10] HAN Mengxue, ZHANG Lin, LIU Xiaoqiang. Subsurface irrigation with ceramic emitters improves wolfberry yield and economic benefits on the Tibetan Plateau, China[J]. Journal of Arid Land, 2023, 15(11): 1376-1390.
[11] Lobna MNIF FAKHFAKH, Mohamed CHAIEB. Effects of water stress on growth phenology photosynthesis and leaf water potential in Stipagrostis ciliata (Desf.) De Winter in North Africa[J]. Journal of Arid Land, 2023, 15(1): 77-90.
[12] WANG Yuxia, ZHANG Jing, YU Xiaojun. Effects of mulch and planting methods on Medicago ruthenica seed yield and soil physical-chemical properties[J]. Journal of Arid Land, 2022, 14(8): 894-909.
[13] WANG Fengjiao, FU Bojie, LIANG Wei, JIN Zhao, ZHANG Liwei, YAN Jianwu, FU Shuyi, GOU Fen. Assessment of drought and its impact on winter wheat yield in the Chinese Loess Plateau[J]. Journal of Arid Land, 2022, 14(7): 771-786.
[14] LI Feng, LI Yaoming, ZHOU Xuewen, YIN Zun, LIU Tie, XIN Qinchuan. Modeling and analyzing supply-demand relationships of water resources in Xinjiang from a perspective of ecosystem services[J]. Journal of Arid Land, 2022, 14(2): 115-138.
[15] CHEN Limei, Abudureheman HALIKE, YAO Kaixuan, WEI Qianqian. Spatiotemporal variation in vegetation net primary productivity and its relationship with meteorological factors in the Tarim River Basin of China from 2001 to 2020 based on the Google Earth Engine[J]. Journal of Arid Land, 2022, 14(12): 1377-1394.