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Effects of nitrogen addition on root respiration of trees and understory herbs at different temperatures in Pinus tabulaeformis forest

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Abstract

Aims

Nitrogen (N) addition had differential effects on root respiration. However, the reasons and mechanism have not yet been analyzed. We speculated that the differential effects of N addition are related to the N addition rate, root diameter, and temperature. Meanwhile, tree and understory herb in forest ecosystems maybe another reason that root respiration has different responses.

Methods

N addition was performed in a Pinus tabulaeformis forest for six years. P. tabulaeformis and Carex lanceolata fine roots with three size classes (< 0.5 mm; 0.5–1.0 mm; 1.0–2.0 mm) were sampled for respiration and temperature sensitivity measurement at three temperatures and chemical analysis.

Results

(1) N addition increased the root respiration of P. tabulaeformis and had the maximum values in 3, 6, and 9 g N m−2 y−1 at 1 °C, 14 °C, and 18 °C, respectively. (2) The root respiration of C. lanceolata significantly decreased under N addition only at 18 °C. (3) The effect of N addition on temperature sensitivity of root respiration was also varied due to N addition rate. (4) N and carbon/nitrogen ratio were the main driving factors of root respiration of P. tabulaeformis, while chemical properties had a slight driving effect on root respiration of C. lanceolata.

Conclusions

N addition rate and temperature were the reasons for the differential effect of N addition on root respiration, but not root diameter. Furthermore, root respirations of tree and understory herb have varied changing mechanism, which demonstrated an apparent species specificity.

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References

  • Antonino DI, Valentino G, Donato C (2015) Acclimation of fine root respiration to soil warming involves starch deposition in very fine and fine roots: a case study in Fagus sylvatica saplings. Physiol Plant 156:294–310

    Google Scholar 

  • Atkin OK, Edwards EJ, Loveys BR (2000) Response of root respiration to changes in temperature and its relevance to global warming. New Phytol 147:141–154

    Article  CAS  Google Scholar 

  • Atkin OK, Zhang Q, Wiskich JT (2002) Effect of temperature on rates of alternative and cytochrome pathway respiration and their relationship with the redox poise of the quinone pool. Plant Physiol 128:212–222

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Atkinson LJ, Hellicar MA, Fitter AH, Atkin OK (2007) Impact of temperature on the relationship between respiration and nitrogen concentration in roots: an analysis of scaling relationships, Q(10) values and thermal acclimation ratios. New Phytol 173:110–120

    Article  CAS  PubMed  Google Scholar 

  • Böhm W (1979) Methods of studying root systems. Springer-Verlag, Berlin

    Book  Google Scholar 

  • Boone RD, Nadelhoffer KJ (1998) Roots exert a strong influence on the temperature sensitivity of soil respiration. Nature 396:570–572

    Article  CAS  Google Scholar 

  • Burton AJ, Pregitzer KS, Ruess RW, Hendrick RL, Allen MF (2002) Root respiration in north American forests: effects of nitrogen concentration and temperature across biomes. Oecologia 131:559–568

    Article  CAS  PubMed  Google Scholar 

  • Burton AJ, Jarvey JC, Jarvi MP, Zak DR, Pregitzer KS (2012) Chronic N deposition alters root respiration-tissue N relationship in northern hardwood forests. Glob Chang Biol 18:258–266

    Article  Google Scholar 

  • Carson AAR, Walter P (2006) On the formation of dense understory layers in forests worldwide: consequences and implications for forest dynamics, biodiversity, and succession. Can J For Res 36:1345–1362

    Article  Google Scholar 

  • Chen D, Zhang Y, Lin Y, Chen H, Fu S (2009) Stand level estimation of root respiration for two subtropical plantations based on in situ measurement of specific root respiration. For Ecol Manag 257:2088–2097

    Article  Google Scholar 

  • Chen D, Zhou R, Rao R, Lin R, Fu R (2010) Effects of root diameter and root nitrogen concentration on in situ root respiration among different seasons and tree species. Ecol Res 25:983–993

    Article  CAS  Google Scholar 

  • Chen H, Li D, Xiao K, Wang K (2018) Soil microbial processes and resource limitation in karst and non-karst forests. Funct Ecol 32:1400–1409

    Article  Google Scholar 

  • Desrochers A, Landhausser SM, Lieffers VJ (2002) Coarse and fine root respiration in aspen (Populus tremuloides). Tree Physiol 22:725–732

    Article  PubMed  Google Scholar 

  • Fu X, Wang J, Wang H, Dai X, Yang F, Zhao M (2016) Response of the fine root production, phenology, and turnover rate of six shrub species from a subtropical forest to a soil moisture gradient and shading. Plant Soil 399:135–146

    Article  CAS  Google Scholar 

  • Galloway JN, Dentener FJ, Capone DG, Boyer EW, Vosmarty CJ (2004) Nitrogen cycles: past, present, and future. Biogeochemistry 70:153–226

    Article  CAS  Google Scholar 

  • Gunn S, Farrar JF (1999) Effects of a 4 °C increase in temperature on partitioning of leaf area and dry mass, root respiration and carbohydrates. Funct Ecol 13:12–20

    Article  Google Scholar 

  • Guo D, Mitchell RJ, Hendricks JJ (2004) Fine root branch orders respond differentially to carbon source-sink manipulations in a longleaf pine forest. Oecologia 140:450–457

    Article  PubMed  Google Scholar 

  • Guo D, Xia M, Wei X, Chang W, Liu Y, Wang Z (2008) Anatomical traits associated with absorption and mycorrhizal colonization are linked to root branch order in twenty-three Chinese temperate tree species. New Phytol 180:673–683

    Article  PubMed  Google Scholar 

  • Hanson PJ, Edwards NT, Garten CT, Andrews JA (2000) Separating root and soil microbial contributions to soil respiration: a review of methods and observations. Biogeochemistry 48:115–146

    Article  CAS  Google Scholar 

  • Haynes BE, Gower ST (1995) Belowground carbon allocation in unfertilized and fertilized red pine plantations in northern Wisconsin. Tree Physiol 5:317–325

    Article  Google Scholar 

  • Huxman TE, Turnipseed AA, Sparks JP, Harley PC, Monson RK (2003) Temperature as a control over ecosystem CO2 fluxes in a high-elevation, subalpine forest. Oecologia 134:537–546

    Article  CAS  PubMed  Google Scholar 

  • Jia S, Wang Z, Li X, Zhang X, Mclaughlin NB (2011) Effect of nitrogen fertilizer, root branch order and temperature on respiration and tissue N concentration of fine roots in Larix gmelinii and Fraxinus mandshurica. Tree Physiol 7:718–726

    Article  Google Scholar 

  • Jia S, Mclaughlin NB, Gu J, Li X, Wang Z (2013) Relationships between root respiration rate and root morphology, chemistry and anatomy in Larix gmelinii and Fraxinus mandshurica. Tree Physiol 6:579–589

    Article  Google Scholar 

  • Jin NN, Kristine C, Li J, Zineb C, Craig B, Stefan A, Peter R, Tjoelker M, Elise P (2020) Does root respiration in Australian rainforest tree seedlings acclimate to experimental warming? Tree Physiol 40:1192–1204

    Article  Google Scholar 

  • Jing H, Wang G (2020) Temporal dynamics of Pinus tabulaeformis litter decomposition under nitrogen addition on the loess plateau of China. For Ecol Manag 476:118465

    Article  Google Scholar 

  • Jing H, Zhou H, Wang G, Xue S, Liu G, Duan M (2017) Nitrogen addition changes the stoichiometry and growth rate of different organs in Pinus tabuliformis seedlings. Front Plant Sci 8:1922

    Article  PubMed  PubMed Central  Google Scholar 

  • Jing H, Zhang P, Li J, Yao X, Liu G, Wang G (2019) Effect of nitrogen addition on the decomposition and release of compounds from fine roots with different diameters: the importance of initial substrate chemistry. Plant Soil 438:281–296

    Article  CAS  Google Scholar 

  • King JS, Pregitzer KS, Zak DR, Holmes WE, Schmidt K (2005) Fine root chemistry and decomposition in model communities of north-temperate tree species show little response to elevated atmospheric CO2 and varying soil resource availability. Oecologia 146:318–328

    Article  CAS  PubMed  Google Scholar 

  • Koch N, Andersen CP, Raidl S, Agerer R, Matyssek R, Grams TEE (2007) Temperature-respiration relationships differ in mycorrhizal and non-mycorrhizal root systems of Picea abies (L.) karst. Plant Biol 9:545–549

    Article  CAS  PubMed  Google Scholar 

  • Leuschner C, Gebel S, Rose L (2013) Root trait responses of six temperate grassland species to intensive mowing and NPK fertilisation: a field study in a temperate grassland. Plant Soil 373:687–698

    Article  CAS  Google Scholar 

  • Li C, Wan S, Zhan C, Din J, Ma B, Yasi R, Xue Z (2020) Effects of nitrogen concentration on root respiration rate and nonstructural carbohydrates of walnut seedlings. Horticult Sci Technol 38:323–331

    CAS  Google Scholar 

  • Lin L, Sun X, Yu Z, Wang K, Zeng DH (2016) Effects of nitrogen addition on microbial respiration and root respiration in a sandy grassland. The J Appl Ecol 27:2189–2196

    CAS  Google Scholar 

  • Lovelock CE, Ruess RW, Feller IC (2006) Fine root respiration in the mangrove Rhizophora mangle over variation in forest stature and nutrient availability. Tree Physiol 26:1601–1606

    Article  CAS  PubMed  Google Scholar 

  • Loveys BR, Atkinson LJ, Sherlock DJ, Roberts RL, Atkin OK (2003) Thermal acclimation of leaf and root respiration: an investigation comparing inherently fast- and slow-growing plant species. Glob Chang Biol 9:895–910

    Article  Google Scholar 

  • Lu R (2000) Methods for soil agrochemistry analysis, vol 5. Agricultural Science and Technology Press, Beijing

    Google Scholar 

  • Mao Q, Lu X, Wang C, Zhou K, Mo J (2017) Responses of understory plant physiological traits to a decade of nitrogen addition in a tropical reforested ecosystem. For Ecol Manag 401:65–74

    Article  Google Scholar 

  • McCormack ML, Dickie IA, Eissenstat DM, Fahey TJ, Fernandez CW, Guo D (2015) Redefining fine roots improves understanding of below-ground contributions to terrestrial biosphere processes. New Phytol 207:505–518

    Article  PubMed  Google Scholar 

  • Mebius LJ (1960) A rapid method for the determination of organic carbon in soil. Anal Chim Acta 22:120–124

    Article  CAS  Google Scholar 

  • Mei L, Gu J, Zhang Z, Wang Z (2010) Responses of fine root mass, length, production and turnover to soil nitrogen fertilization in Larix gmelinii and Fraxinus mandshurica forests in northeastern China. J For Res 15:194–201

    Article  CAS  Google Scholar 

  • Mo J, Zhang W, Zhu W, Gundersen P, Fang Y, Li D, Wang H (2007) Nitrogen addition reduces soil respiration in a mature tropical forest in southern China. Glob Chang Biol 2:403–412

    Google Scholar 

  • Oechel WTL, Walter C (1983) Effects of soil temperature on the carbon exchange of taiga seedlings: I. root respiration. Revue Canadienne De Recherche Forestière 13:840–849

    Article  Google Scholar 

  • Page AL, Miller RH, Keeney DR (1982) Methods of soil analysis. Catena 15:99–100

    Google Scholar 

  • Parts K, Tedersoo L, Schindlbacher A, Sigurdsson BD, Leblans NIW, Oddsdottir ES, Borken W, Ostonen I (2019) Acclimation of fine root systems to soil warming: comparison of an experimental setup and a natural soil temperature gradient. Ecosystems 22:457–472

    Article  CAS  Google Scholar 

  • Pregitzer KS, Deforest JL, Burton AJ, Allen MF, Ruess RW, Hendrick RL (2002) Fine root architecture of nine north American trees. Ecol Monogr 72:293–309

    Article  Google Scholar 

  • Raich JW, Schlesinger WH (1992) The global carbon dioxide flux in soil respiration and its relationship to vegetation and climate. Tellus 44:81–99

    Article  Google Scholar 

  • Ryan MG (1991) Effects of climate change on plant respiration. Ecol Appl 1:157–167

    Article  PubMed  Google Scholar 

  • Ryan MG, Hubbard RM, Pongracic S, Raison RJ, Mcmurtrie RE (1996) Foliage, fine-root, woody-tissue and stand respiration in Pinus radiata in relation to nitrogen status. Tree Physiol 16:333–343

    Article  CAS  PubMed  Google Scholar 

  • Scheller RM, Mladenoff DJ (2002) Understory species patterns and diversity in old-growth and managed northern hardwood forests. Ecol Appl 12:1329–1343

    Article  Google Scholar 

  • Schleser GH (1982) The response of CO2 evolution from soils to global temperature changes. Ztschrift Für Naturforschung A 37:287–291

    Article  Google Scholar 

  • Sun L, Jing H, Wang G, Liu G (2018) Nitrogen addition increases the contents of glomalin-related soil protein and soil organic carbon but retains aggregate stability in a Pinus tabulaeformis forest. PeerJ 6: e5039

  • Sundareshwar PV, Morris JT, Koepfler EK, Fornwalt B (2003) Phosphorus limitation of coastal ecosystem processes. Science 299:563–565

    Article  CAS  PubMed  Google Scholar 

  • Vidya S, Nishanth T, Elise P, Rao AM (2017) Warming and elevated CO2 alter the suberin chemistry in roots of photosynthetically divergent grass species. AoB Plants 5:5

    Google Scholar 

  • Wang Z, Zheng F (2018) C, N, and P stoichiometric characteristics of Pinus tabulaeformis plantation in the Ziwuling region of the loess plateau. Acta Ecol Sin 38:11

    Google Scholar 

  • Wang W, Peng S, Fang J (2010) Root respiration and its relation to nutrient contents in soil and root and EVI among 8 ecosystems, northern China. Plant Soil 333:391–401

    Article  CAS  Google Scholar 

  • Wang Z, Huang H, Deng J, Liu J (2015) Scaling the respiratory metabolism to phosphorus relationship in plant seedlings. Sci Rep 5:16377

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Wang G, Xue S, Liu F, Liu G (2017) Nitrogen addition increases the production and turnover of the lower-order roots but not of the higher-order roots of Bothriochloa ischaemum. Plant Soil 415:423–434

    Article  CAS  Google Scholar 

  • Wei Y, Tong Y, Qiao L, Liu X, Duan M, Li J (2010) Preliminary estimate of the atmospheric nitrogen deposition in different ecological regions of Shaanxi Province. J Agro-Environ Sci 29:795–800

    CAS  Google Scholar 

  • Wei L, Su J, Jing G, Zhao J, Liu J, Cheng J, Jin J (2018) Nitrogen addition decreased soil respiration and its components in a long-term fenced grassland on the loess plateau. J Arid Environ 152:37–44

    Article  Google Scholar 

  • Wise CS, Dimler RJ, Davis HA, Rist CE (1955) Determination of easily hydrolyzable fructose units in dextran preparations. Anal Chem 27:33–36

    Article  CAS  Google Scholar 

  • Wu J, Liu Z, Chen D, Huang G, Zhou L, Fu S (2011) Understory plants can make substantial contributions to soil respiration: evidence from two subtropical plantations. Soil Biol Biochem 43:2355–2357

    Article  CAS  Google Scholar 

  • Yang Y, Dong B, Xie J, Chen G, Gao R, Li L, Wang X, Guo J (2004) Soil respiration of forest ecosystems and its respondence to global change. Acta Ecol Sin 24:583–591

  • Zeng W, Zhang J, Wang W (2018) Strong root respiration response to nitrogen and phosphorus addition in nitrogen-limited temperate forests. Sci Total Environ 642:646–655

    Article  CAS  PubMed  Google Scholar 

  • Zhang C, Niu D, Hall S, Wen H, Li X, Fu H, Wan C, Elser J (2014) Effects of simulated nitrogen deposition on soil respiration components and their temperature sensitivities in a semiarid grassland. Soil Biol Biochem 75:113–123

    Article  CAS  Google Scholar 

  • Zhang J, Ai Z, Liang C, Wang G, Xue S (2017) Response of soil microbial communities and nitrogen thresholds of Bothriochloa ischaemum to short-term nitrogen addition on the loess plateau. Geoderma 308:112–119

    Article  CAS  Google Scholar 

  • Zhang Y, Dang S, Guo S (2019) Root respiration and its temperature sensitivity at various growth stages of winter wheat in the loess plateau, Northwest China. J Appl Ecol 30:3762–3770

    Google Scholar 

  • Zhu C, Ma Y, Wu H, Sun T, La Pierre KJ, Sun Z, Yu Q (2016) Divergent effects of nitrogen addition on soil respiration in a semiarid grassland. Sci Rep 6:33541

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Zhu L, Gu G, Xu Z, You C, Mu L, Ding S, Zeng X, Wu F (2019) Ecological stoichiometric ratio of carbon, nitrogen, and phosphorus in tree, shrub, and herb species in a subtropical evergreen broad-leaved forest. Chin J Appl Environ Biol 25:1277–1285

    Google Scholar 

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Funding

This research was funded by the National Natural Science Foundation of China (No. 41671513) and the National Key Research and Development Program of China (2017YFC0504601).

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Correspondence to Guoliang Wang.

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Responsible Editor: Hans Lambers.

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Research highlights

• Root respiration of P. tabulaeformis had the maximum values in 3, 6, and 9 g of N m−2 y−1 at 1 °C, 14 °C, and 18 °C, respectively.

• Root respiration of C. lanceolata significantly decreased to N addition only at 18 °C.

• Temperature sensitivity of root respiration had varied responses to N addition due to the N addition rate.

• N, C/N and non-structural carbohydrate were the driving factors of root respiration of P. tabulaeformis, but not of C. lanceolata.

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Jing, H., Liu, Y., Wang, G. et al. Effects of nitrogen addition on root respiration of trees and understory herbs at different temperatures in Pinus tabulaeformis forest. Plant Soil 463, 447–459 (2021). https://doi.org/10.1007/s11104-021-04925-w

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