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Local edaphic factors influence leaf nutrient resorption efficiency of evergreen and deciduous trees: a case study from montane subtropical old-growth and regenerating forests of Meghalaya

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Abstract

Variation in soil nutrient availability can influence the functional traits and performance of tree species in a forested landscape. We tested this hypothesis by studying the variations in leaf-traits, and N- and P-resorption efficiencies of a few evergreen (Myrica esculenta, Rhododendron arboretum and Lithocarpus dealbatus) and deciduous (Quercus griffithii, Engelhardtia spicata and Lyonia ovalifolia) tree species growing in montane subtropical old-growth and regenerating forests of Meghalaya, northeast India, varying in their soil characteristics. Trees of the old-growth forest stand, having greater soil total N and P, proved to be much efficient in their foliar nutrient resorption (mean = 42.0% for N and mean = 82.1% for P) and showed higher leaf nutritional quality compared to the regenerating forest stand. Deciduous species had greater N-resorption efficiencies (45.3–49.7%) than the evergreen species (23.6–56.9%) in the old-growth stand. However, in the regenerating stand, the evergreen species were better at resorbing both N (30.6–55.9%) and P (67.9–76.4%) from their leaves than the deciduous species (23.2–40.9% for N and 33.2–52.0% for P). Overall, phosphorus was the limiting nutrient for growth in both the functional groups, with relatively low concentrations in the soils of the two forest stands. The evergreen and deciduous trees in the old-growth forest are found to tightly conserve nutrients with higher leaf N and P concentrations and higher N- and P- resorption efficiencies than the regenerating forest stand. The study clearly indicates that soil fertility has profound effect on the internal nutrient cycling of evergreen and deciduous tree species.

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References

  • Aerts R (1990) Nutrient use efficiency in evergreen and deciduous species from heathland. Oecologia 84:391–397

    PubMed  Google Scholar 

  • Aerts R (1996) Nutrient resorption from senescing leaves of perennials: are there general patterns? J Ecol 84:597–608

    Google Scholar 

  • Aerts RS, Chapin FIII (2000) The mineral nutrition of wild plants revisited: a re-evaluation of processes and patterns. Adv Ecol Res 30:1–67

    CAS  Google Scholar 

  • Allen SE, Grimshaw HM, Parkinson JA, Quarmby C (1974) Chemical analysis of ecological materials. Blackwell Scientific Publications, Oxford

    Google Scholar 

  • Boerner REJ (1986) Seasonal nutrient dynamics, nutrient resorption and mycorrhizal infection intensity of two perennial forest herbs. Am J Bot 73:1249–1257

    Google Scholar 

  • Brant AN, Chen HYH (2015) Patterns and mechanisms of nutrient resorption in plants. Crti Rev Plant Sci 34:471–486

    CAS  Google Scholar 

  • Chapin FSIII, Kedrowski RA (1983) Seasonal changes in nitrogen and phosphorus fractions and autumn retranslocation in evergreen and deciduous taiga trees. Ecology 64:376–391

    CAS  Google Scholar 

  • Chapin FSIII, Moilanen L, Kielland K (1993) Preferential use of organic nitrogen for growth by a non-mycorrhizal arctic sedge. Nature 361:150–153

    CAS  Google Scholar 

  • Chen Y, Han W, Tang L, Tang Z, Fang J (2013) Leaf nitrogen and phosphorus concentrations of woody plants differ in responses to climate, soil and plant growth form. Ecography 36:178–184

    Google Scholar 

  • Chen FS, Niklas KJ, Liu Y, Fang XM, Wan SZ, Wang H (2015) Nitrogen and phosphorus additions alter nutrient dynamics but not resorption efficiencies of Chinese fir leaves and twigs differing in age. Tree Physiol 35:1106–1117

    CAS  PubMed  Google Scholar 

  • Cornelissen JHC, Pérez-Harguindeguy N, Díaz S, Grime JP, Marzano B, Cabido M, Vendramini F, Cerabolini B (1999) Leaf structure and defence control litter decomposition rate across species and life forms in regional flora on two continents. New Phytol 143:191–200

    Google Scholar 

  • Distel RA, Moretto AS, Didone NG (2003) Nutrient resorption from senescing leaves in two Stipa species native to central Argentina. Austral Ecol 28:210–215

    Google Scholar 

  • Eckstein RL, Karlsson PS, Weih M (1999) Life span and nutrient resorption as determinants of plant nutrient conservation in temperate–arctic regions. New Phytol 143:177–190

    Google Scholar 

  • Elser JJ, Bracken MES, Cleland EE, Gruner DS, Harpole WS, Hillebrand H, Ngai JT, Seabloom EW, Shurin JB, Smith JE (2007) Global analysis of nitrogen and phosphorus limitation of primary producers in freshwater, marine and terrestrial ecosystems. Ecol Lett 10:1135–1142

    PubMed  Google Scholar 

  • Enoki T, Kawaguchi H (1999) Nitrogen resorption from needles of Pinus thunbergii Parl. growing along a topographic gradient of soil nutrient availability. Ecol Res 14:1–8

    Google Scholar 

  • Gallardo A, Merino J (1999) Control of leaf litter decomposition rate in a Mediterranean shrubland as indicated by N, P and lignin concentrations. Pedobiol (Jena) 43:64–72

    Google Scholar 

  • Givnish TJ (2002) Adaptive significance of evergreen vs. deciduous leaves: solving the triple paradox. Silva Fenn 36:703–743

    Google Scholar 

  • Gower ST, McMurtrie RE, Murty D (1996) Aboveground net primary production decline with stand age: potential causes. Trends Ecol Evol 11:378–382

    CAS  PubMed  Google Scholar 

  • Güsewell S (2004) N: P ratios in terrestrial plants: variation and functional significance. New Phytol 164:243–266

    Google Scholar 

  • Hagen-Thorn A, Varnagiryte I, Nihlgard B, Armolaitis K (2006) Autumn nutrient resorption and losses in four deciduous forest tree species. Forest Ecol Manag 228:33–39

    Google Scholar 

  • Hammer Ø, Harper DAT, Ryan PD (2001) PAST: paleontological statistics software package for education and data analysis. Palaeontol Electronica 4:9

    Google Scholar 

  • Han W, Tang L, Chen Y, Fang J (2013) Relationship between the relative limitation and resorption efficiency of nitrogen vs phosphorus in woody plants. PLoS One 8:e83366

    PubMed  PubMed Central  Google Scholar 

  • Hayes P, Turner BL, Lambers H, Laliberté E (2014) Foliar nutrient concentrations and resorption efficiency in plants of contrasting nutrient–acquisition strategies along a 2–million–year dune chronosequence. J Ecol 102:396–410

    CAS  Google Scholar 

  • He JS, Wang X, Schmid B, Flynn DFB, Li X, Reich PB, Fang J (2010) Taxonomic identity, phylogeny, climate and soil fertility as drivers of leaf traits across Chinese grassland biomes. J Plant Res 123:551–561

    PubMed  Google Scholar 

  • Hidaka A, Kitayama K (2011) Allocation of foliar phosphorus fractions and leaf traits of tropical tree species in response to decreased soil phosphorus availability on Mount Kinabalu, Borneo. J Ecol 99:849–857

    CAS  Google Scholar 

  • Hobbie S (1992) Effects of plant species on nutrient cycling. Trends Ecol Evol 7:336–339

    CAS  Google Scholar 

  • Huang JJ, Boerner REJ (2007) Effects of fire alone or combined with thinning on tissue nutrient concentrations and nutrient resorption in Desmodium nudiflorum. Oecologia 153:233–243

    PubMed  Google Scholar 

  • Huang J, Wang XH, Yan ER (2007) Leaf nutrient concentration, nutrient resorption and litter decomposition in an evergreen broad–leaved forest in eastern China. Forest Ecol Manag 239:150–158

    Google Scholar 

  • Kamei J, Pandey HN, Barik SK (2009) Tree species distribution and its impact on soil properties, and nitrogen and phosphorus mineralization in a humid subtropical forest ecosystem of northeastern India. Can J For Res 39(1):36–47

    CAS  Google Scholar 

  • Killingbeck KT (1996) Nutrients in senesced leaves: keys to the search for potential resorption and resorption proficiency. Ecology 77:1716–1727

    Google Scholar 

  • Knecht MF, Göransson A (2004) Terrestrial plants require nutrients in similar proportions. Tree Physiol 24:447–460

    CAS  PubMed  Google Scholar 

  • Kobe RK, Lepczyk CA, Iyer M (2005) Resorption efficiency decreases with increasing green leaf nutrients in a global data set. Ecology 86:2780–2792

    Google Scholar 

  • Koerselman W, Meuleman AFM (1996) The vegetation N: P ratio: a new tool to detect the nature of nutrient limitation. J Appl Ecol 33:1441–1450

    Google Scholar 

  • Lal CB, Annapurna C, Raghubanshi AS, Singh JS (2001) Effect of leaf habit and soil type on nutrient resorption and conservation in woody species of a dry tropical environment. Can J Bot 79:1066–1075

    CAS  Google Scholar 

  • Lambers H, Brundrett MC, Ravel JA, Hopper SD (2010) Plant mineral nutrition in ancient landscapes: high plant species diversity on infertile soils is linked to functional diversity for nutritional strategies. Plant Soil 334:11–31

    CAS  Google Scholar 

  • Lehtonen A, Sievänen R, Mäkelä A, Mäkipää R, Korhonen KT, Hokkanen T (2004) Potential litterfall of Scots pine branches in southern Finland. Ecol Model 180:305–315

    CAS  Google Scholar 

  • Li Y, Yang F, Ou Y, Zhang D, Liu J, Chu G, Zhang Y, Otieno D, Zhou G (2013) Changes in forest soil properties in different successional stages in lower tropical China. PLoS One 8:11

    Google Scholar 

  • Li X, Liu J, Fan J, Ma Y, Ding S, Zhong Z, Wang D (2015) Combined effects of nitrogen addition and litter manipulation on nutrient resorption of Leymus chinensis in a semi-arid grassland of northern China. Plant Biol 17:9–15

    PubMed  Google Scholar 

  • Liu XZ, Zhou GY, Zhang DQ, Liu SZ, Chu GW, Yan JH, He JS, Han XG (2010) N and P stoichiometry of plant and soil in lower subtropical forest successional series in southern China. J Plant Ecol (Chin Vers) 34:64–71

    CAS  Google Scholar 

  • Miatto RC, Wright IJ, Batalha MA (2016) Relationships between soil nutrient status and nutrient-related leaf traits in Brazilian cerrado and seasonal forest communities. Plant Soil 404:13–33

    CAS  Google Scholar 

  • Nambiar EKS, Fife DN (1987) Growth and nutrient retranslocation in needles of radiata pine in relation to nitrogen supply. Ann Bot 60:147–156

    Google Scholar 

  • Niinemets U (1999) Components of leaf dry mass per area—thickness and density—alter leaf photosynthetic capacity in reverse directions in woody plants. New Phytol 144:35–47

    Google Scholar 

  • Niinemets U (2001) Global–scale climatic controls of leaf dry mass per area, density, and thickness in trees and shrubs. Ecology 82:453–469

    Google Scholar 

  • Norby RJ, Long TM, Hartz-Rubin JS, O’Neill EG (2000) Nitrogen resorption in senescing tree leaves in a warmer, CO2-enriched atmosphere. Plant Soil 224:15–29

    CAS  Google Scholar 

  • Ordonez JC, Van Bodegom PM, Witte JPM, Wright IJ, Reich PB, Aerts R (2009) A global study of relationships between leaf traits, climate and soil measures of nutrient fertility. Glob Ecol Biogeogr 18:137–149

    Google Scholar 

  • Palow DT, Nolting K, Kitajima K (2012) Functional trait divergence of juveniles and adults of nine Inga species with contrasting soil preference in a tropical rain forest. Funct Ecol 26:1144–1152

    Google Scholar 

  • Poorter H, Garnier E (1999) Ecological significance of inherent variation in relative growth rate and its components. In: Pugnaire FI, Valladares F (eds) Handbook of functional plant ecology. Marcel Dekker, New York, pp 81–120

    Google Scholar 

  • Poorter H, Niinemets U, Poorter L, Wright IJ, Villar R (2009) Causes and consequences of variation in leaf mass per area (LMA): a meta–analysis. New Phytol 182:565–588

    Google Scholar 

  • Rahman MM, Tsukamoto J (2013) Leaf traits, litter decomposability and forest floor dynamics in an evergreen- and a deciduous-broadleaved forest in warm temperate Japan. Forestry 2013:1–11

    Google Scholar 

  • Reich PB, Wright IJ, Cavender-Bares J, Craine JM, Oleksyn J, Westoby M, Walters MB (2003) The evolution of plant functional variation: traits, spectra, and strategies. Int J Plant Sci 164:S143–S164

    Google Scholar 

  • Rejmánková E (2005) Nutrient resorption in wetland macrophytes: comparison across several regions of different nutrient status. New Phytol 167:471–482

    PubMed  Google Scholar 

  • Rentería LY, Jaramillo VJ (2011) Rainfall drives leaf traits and leaf nutrient resorption in a tropical dry forest in Mexico. Oecologia 165:201–211

    PubMed  Google Scholar 

  • Rentería LY, Jaramillo VJ, Martínez-Yrízar A, Pérez-Jiménez A (2005) Nitrogen and phosphorus resorption in trees of a Mexican tropical dry forest. Trees 19:431–441

    Google Scholar 

  • Richardson SJ, Allen RB, Doherty JE (2008) Shifts in leaf N: P ratio during resorption reflect soil P in temperate rainforest. Funct Ecol 22:738–745

    Google Scholar 

  • Sabaté S, Sala A, Garcia CA (1995) Nutrient content in Quercus ilex canopies: seasonal and spatial variation within a catchment. Plant Soil 168–169:297–304

    Google Scholar 

  • Salazar S, Sánchez LE, Galindo P, Santa-Regina I (2011) N and P resorption efficiency and proficiency from leaves under different forest management systems of deciduous woody species. Int Res J Eng Tech 3:389–397

    Google Scholar 

  • Sariyildiz T, Savaci G, Kravkaz IS (2015) Effects of tree species, stand age and land-use change on soil carbon and nitrogen stock rates in northwestern Turkey. Biogeosci Forestry 9:165–170

    Google Scholar 

  • Sasser CL, Binkley D (1989) Nitrogen mineralization in high-elevation forests of the Appalachians. II. Patterns with stand development in fir waves. Biogeochemistry 7:147–156

    Google Scholar 

  • Tang L, Han W, Chen Y, Fang J (2013) Resorption proficiency and efficiency of leaf nutrients in woody plants in eastern China. J Plant Ecol 6:408–417

    Google Scholar 

  • Tang J, Luyssaert S, Richardson AD, Kutsch W, Janssens IA (2014) Steeper declines in forest photosynthesis than respiration explain age-driven decreases in forest growth. Proc Natl Acad Sci USA 111:8856–8860

    CAS  PubMed  Google Scholar 

  • Tomlinson KW, Van Langevelde F, Ward D, Bongers F, da Silva DA, Prins HHT, de Bie S, Sterck FJ (2013) Deciduous and evergreen trees differ in juvenile biomass allometries because of differences in allocation to root storage. Ann Bot 112:575–587

    CAS  PubMed  PubMed Central  Google Scholar 

  • Van Heerwaarden OJ, Toet S, Aerts R (2003) Current measures of nutrient resorption efficiency lead to a substantial underestimation of real resorption efficiency: facts and solutions. Oikos 101:664–669

    Google Scholar 

  • Vance CP, Uhde-Stone C, Allan DL (2003) Phosphorus acquisition and use: critical adaptations by plants for securing a nonrenewable resource. New Phytol 157:423–447

    CAS  Google Scholar 

  • Vergutz L, Manzoni S, Porporato A, Novai RF, Jackson RB (2012) Global resorption efficiencies and concentrations of carbon and nutrients in leaves of terrestrial plants. Ecol Monogr 82:205–220

    Google Scholar 

  • Vile D, Garnier E, Shipley B, Laurent G, Navas ML, Roumet C, Lavorel S, Diaz S, Hodgson JG, Lloret F, Midgley GF, Poorter H, Rutherford MC, Wilson PJ, Wright IJ (2005) Specific leaf area and dry matter content estimate thickness in laminar leaves. Ann Bot 96:1129–1136

    PubMed  PubMed Central  Google Scholar 

  • Violle C, Navas ML, Vile D, Kazakou E, Fortunel C, Hummel I, Garnier E (2007) Let the concept of trait be functional! Oikos 116:882–892

    Google Scholar 

  • Wardle DA, Walker LR, Bardgett RD (2004) Ecosystem properties and forest decline in contrasting long-term chronosequences. Science 305:509–513

    CAS  PubMed  Google Scholar 

  • Westoby M, Falster DS, Moles AT, Vesk PA, Wright IJ (2002) Plant ecological strategies: some leading dimensions of variation between species. Annu Rev Ecol Syst 33:125–159

    Google Scholar 

  • Wright IJ, Cannon K (2001) Relationships between leaf lifespan and structural defenses in a low–nutrient, sclerophyll flora. Funct Ecol 15:351–359

    Google Scholar 

  • Wright IJ, Westoby M (2003) Nutrient concentration, resorption and lifespan: leaf traits of Australian sclerophyll species. Funct Ecol 17:10–19

    Google Scholar 

  • Wright IJ, Reich PB, Westoby M, Ackerly DD, Baruch Z, Bongers F, Cavender-Bares J, Chapin FS, Cornelissen JHC, Diemer M, Flexas J, Garnier E, Groom PK, Gulias J, Hikosaka K, Lamont BB, Lee T, Lee W, Lusk C, Midgley JJ, Navas ML, Niinemets U, Oleksyn J, Osada N, Poorter H, Poot P, Prior L, Pyankov VI, Roumet C, Thomas SC, Tjoelker MG, Veneklaas EJ, Villar R (2004) The world–wide leaf economics spectrum. Nature 428:821–827

    CAS  Google Scholar 

  • Yan T, Jiaojun Z, Kai Y (2018) Leaf nitrogen and phosphorus resorption of woody species in response to climatic conditions and soil nutrients: a meta-analysis. J For Res 29:905–913

    CAS  Google Scholar 

  • Yang H (2018) Effects of nitrogen and phosphorus addition on leaf nutrient characteristics in a subtropical forest. Trees 32:383–391

    CAS  Google Scholar 

  • Yesilonis I, Szlavecz K, Pouyat R, Whigham D, Xia L (2016) Historical land use and stand age effects on forest soil properties in the Mid-Atlantic US. For Ecol Manage 370:83–92

    Google Scholar 

  • Zhang C, Tian HQ, Liu JY, Wang SQ, Liu ML, Pan SF, Shi XZ (2005) Pools and distributions of soil phosphorus in China. Glob Biogeochem Cycles 19:GB1020

    Google Scholar 

  • Zhang YJ, Yang QY, Lee DW, Goldstein G, Cao KF (2013) Extended leaf senescence promotes carbon gain and nutrient resorption: importance of maintaining winter photosynthesis in subtropical forests. Oecologia 173:721–730

    PubMed  Google Scholar 

  • Zhou L, Addo-Danso SD, Wu P, Li S, Zou X, Zhang Y, Ma X (2016) Leaf resorption efficiency in relation to foliar and soil nutrient concentrations and stoichiometry of Cunninghamia lanceolata with stand development in southern China. J Soils Sediments 16:1–12

    Google Scholar 

  • Zhu F, Lu X, Mo J (2014) Phosphorus limitation on photosynthesis of two dominant understory species in a lowland tropical forest. J Plant Ecol 7:526–534

    Google Scholar 

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Authors and Affiliations

  1. Department of Botany, North-Eastern Hill University, Shillong, 793022, India

    Namita Thapa & N. John Lakadong

  2. CSIR-National Botanical Research Institute, Lucknow, India

    Saroj K. Barik

  3. Division of Environmental Sciences, Department of Basic Sciences and Social Sciences, North-Eastern Hill University, Shillong, 793022, India

    Krishna Upadhaya

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  1. Namita Thapa
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Correspondence to Saroj K. Barik.

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Thapa, N., Barik, S.K., Upadhaya, K. et al. Local edaphic factors influence leaf nutrient resorption efficiency of evergreen and deciduous trees: a case study from montane subtropical old-growth and regenerating forests of Meghalaya. Trop Ecol 61, 21–31 (2020). https://doi.org/10.1007/s42965-020-00063-z

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