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Changes in defense traits of young leaves in subtropical forests succession

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Abstract

Plants develop diverse adaptive traits in changeable environments, yet whether plant defense traits change during succession remains unclear. In this study, we investigated the young leaf physical traits (i.e., upright orientation of leaves, trichomes, an enhanced cuticle, and a multilayered epidermis) and leaf color trait (i.e., red pigmentation) of dominant plants in three subtropical forests. These forests included a pioneer forest, a mixed coniferous-broadleaved forest, and a monsoon-evergreen broadleaved forest representing early, middle, and later successional stages, respectively. Our results show that the red color trait in young leaves is related to anti-herbivory defense, and the percentage of species with red young leaves is higher in later than in early succession. Physical defense tends to be weaker for red young leaves than for green young leaves in early and middle successions. In addition, the number of defense traits of young leaves increases with succession. We speculate that young leaves in subtropical forests depend increasingly on multiple defense traits during succession because of the increased biotic stresses and environmental complexity in later succession.

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References

  • Agrawal AA (2011) Current trends in the evolutionary ecology of plant defence. Funct Ecol 25:420–432

    Article  Google Scholar 

  • Agrawal AA, Fishbein M (2006) Plant defense syndromes. Ecology 87:132–149

    Article  Google Scholar 

  • Archetti M, Döring TF, Hagen SB, Hughes NM, Leather SR, Lee DW, Lev-Yadun S, Manetas Y, Ougham HJ, Schaberg PG, Thomas H (2009) Unravelling the evolution of autumn colours: an interdisciplinary approach. Trends Ecol Evol 24:166–173

    Article  PubMed  Google Scholar 

  • Bari R, Jones JD (2009) Role of plant hormones in plant defence responses. Plant Mol Biol 69:473–488

    Article  CAS  Google Scholar 

  • Barton KE, Koricheva J (2010) The ontogeny of plant defense and herbivory: Characterizing general patterns using meta-analysis. Am Nat 175:481–493

    Article  Google Scholar 

  • Bennett RN, Wallsgrove RM (2006) Secondary metabolites in plant defence mechanisms. New Phytol 127:617–633

    Article  Google Scholar 

  • Chabot BF, Hicks DJ (1982) The ecology of leaf life spans. Annu Rev Ecol Syst 13:229–259

    Article  Google Scholar 

  • Chassot C, Nawrath C, Métraux JP (2008) The cuticle: Not only a barrier for plant defence: A novel defence syndrome in plants with cuticular defects. Plant Signal Behav 3:142–144

    Article  PubMed  PubMed Central  Google Scholar 

  • Chen YZ, Huang SQ (2013) Red young leaves have less mechanical defence than green young leaves. Oikos 122:1035–1041

    Article  Google Scholar 

  • Coley PD, Barone JA (1996) Herbivory and plant defenses in tropical forests. Annu Rev Ecol Systemat 27:305–335

    Article  Google Scholar 

  • Dalin P, Björkman C (2003) Adult beetle grazing induces willow trichome defence against subsequent larval feeding. Oecologia 134:112–118

    Article  PubMed  Google Scholar 

  • Davidson DW (1993) The effects of herbivory and granivory on terrestrial plant succession. Oikos 68:23–35

    Article  Google Scholar 

  • Eichenberg D, Purschke O, Ristok C, Wessjohann L, Bruelheide H (2015) Trade-offs between physical and chemical carbon-based leaf defence: of intraspecific variation and trait evolution. J Ecol 103:1667–1679

    Article  CAS  Google Scholar 

  • Erickson AA, Bell SS, Dawes CJ (2004) Does mangrove leaf chemistry help explain crab herbivory patterns? Biotropica 36:333–343

    Google Scholar 

  • Grotewold E (2006) The genetics and biochemistry of floral pigments. Annu. Rev. Plant Biol 57:761–780

    Article  CAS  PubMed  Google Scholar 

  • Guo Q (2003) Temporal species richness-biomass relationships along successional gradients. J Veg Sci 14:121–128

    Article  Google Scholar 

  • Gutschick VP (1999) Biotic and abiotic consequences of differences in leaf structure. New Phytol 143:3–18

    Article  Google Scholar 

  • Gutterman Y, Chauser-Volfson E (2000) The distribution of the phenolic metabolites barbaloin, aloeresin and aloenin as a peripheral defense strategy in the succulent leaf parts of aloe arborescens. Biochem Syst Ecol 28:825–838

    Article  CAS  PubMed  Google Scholar 

  • Hakes AS, Cronin JT (2011) Environmental heterogeneity and spatiotemporal variability in plant defense traits. Oikos 120:452–462

    Article  Google Scholar 

  • Hanley ME, Lamont BB, Fairbanks MM, Rafferty CM (2007) Plant structural traits and their role in anti-herbivore defence. Perspect Plant Ecol 8:157–178

    Article  Google Scholar 

  • Heil M, Ton J (2008) Long-distance signalling in plant defence. Trends Plant Sci 13:264–272

    Article  CAS  Google Scholar 

  • Herms DA, Mattson WJ (1992) The dilemma of plants: to grow or defend. Q Rev Biol 67:283–335

    Article  Google Scholar 

  • Iii FSC, Pugnaire F (1993) Evolution of suites of traits in response to environmental stress. Am Nat 142:S78–S92

    Article  Google Scholar 

  • Kachroo A, Kachroo P (2009) Fatty acid-derived signals in plant defense. Annu Rev Phytopathol 47:153–176

    Article  CAS  PubMed  Google Scholar 

  • Kirkwood RC (1999) Recent developments in our understanding of the plant cuticle as a barrier to the foliar uptake of pesticides. J Pestic Sci 55:69–77

    Article  CAS  Google Scholar 

  • Kursar TA, Coley PD (1992) Delayed greening in tropical leaves: an antiherbivore defense? Biotropica 24:256–262

    Article  Google Scholar 

  • Lamont BB, Groom PK, Cowling RM (2002) High leaf mass per area of related species assemblages may reflect low rainfall and carbon isotope discrimination rather than low phosphorus and nitrogen concentrations. Funct Ecol 16:403–412

    Article  Google Scholar 

  • Landi M, Tattini M, Gould KS (2015) Multiple functional roles of anthocyanins in plant-environment interactions. Environ Exp Bot 119:4–17

    Article  CAS  Google Scholar 

  • Lee DW, Gould KS (2002) Anthocyanins in leaves and other vegetative organs: An introduction. Adv Bot Res 37:1–16

    Article  CAS  Google Scholar 

  • Levin DA (1973) The role of trichomes in plant defense. Q Rev Biol 48:3–15

    Article  Google Scholar 

  • Liu J, Yan HF, Newmaster SG, Pei N, Ragupathy S, Ge XJ (2015) The use of DNA barcoding as a tool for the conservation biogeography of subtropical forests in China. Divers Distrib 21:188–199

    Article  Google Scholar 

  • Manetas Y, Drinia A, Petropoulou Y (2002) High contents of anthocyanins in young leaves are correlated with low pools of xanthophyll cycle components and low risk of photoinhibition. Photosynthetica 40:349–354

    Article  CAS  Google Scholar 

  • Manetas Y (2003) The importance of being hairy: The adverse effects of hair removal on stem photosynthesis of verbascum speciosum are due to solar UV-B radiation. New Phytol 158:503–508

    Article  Google Scholar 

  • Martin JT (2003) Role of cuticle in the defense against plant disease. Annu Rev Phytopathol 2:81–100

    Article  Google Scholar 

  • Mittler R (2002) Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci 7:405–410

    Article  CAS  PubMed  Google Scholar 

  • Moles AT, Bonser SP, Poore AG, Wallis IR, Foley WJ (2011) Assessing the evidence for latitudinal gradients in plant defence and herbivory. Funct Ecol 25:380–388

    Article  Google Scholar 

  • Peng SL (1996) Community dynamics of lower subtropical forests. Science Press, Beijing

    Google Scholar 

  • Peng SL, Ren H (1998) The energy ecology study in sub-tropical forest ecosystem. China Meteorological Press, Beijing

    Google Scholar 

  • Pritsch C, Muehlbauer GJ, Bushnell WR, Somers DA, Vance CP (2000) Fungal development and induction of defense response genes during early infection of wheat spikes by fusarium graminearum. Mol Plant Microbe In 13:159–169

    Article  CAS  Google Scholar 

  • Raevel V, Violle C, Munoz F (2012) Mechanisms of ecological succession: Insights from plant functional strategies. Oikos 121:1761–1770

    Article  Google Scholar 

  • Sangoi L, Gracietti M, Rampazzo C, Bianchetti P (2002) Response of brazilian maize hybrids from different eras to changes in plant density. Field Crop Res 79:39–51

    Article  Google Scholar 

  • Schaefer HM, Wilkinson DM (2004) Red leaves, insects and coevolution: a red herring? Trends Ecol Evol 19:616–618

    Article  PubMed  Google Scholar 

  • Serrano M, Coluccia F, Torres M, L'Haridon F, Métraux JP (2014) The cuticle and plant defense to pathogens. Front Plant Sci 5:274

    Article  PubMed  PubMed Central  Google Scholar 

  • Tattini M, Landi M, Brunetti C, Giordano C, Remorini D, Gould KS, Guidi L (2014) Epidermal coumaroyl anthocyanins protect sweet basil against excess light stress: multiple consequences of light attenuation. Physiol Plant 152:585–598

    Article  CAS  PubMed  Google Scholar 

  • Wagner GJ (1991) Secreting glandular trichomes: More than just hairs. Plant Physiol 96:675–679

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Woodman RL, Fernandes GW (1991) Differential mechanical defense : herbivory, evapotranspiration, and leaf-hairs. Oikos 60:11–19

    Article  Google Scholar 

  • Wu F, Yu Y, Sun J, Zhang J, Wang J, Tang G, Wang Y (2016) Characteristics, source apportionment and reactivity of ambient volatile organic compounds at Dinghu mountain in Guangdong Province, China. Sci Total Environ 548:347–359

    Article  CAS  PubMed  Google Scholar 

  • Zhou G, Guan L, Wei X, Zhang D, Zhang Q, Yan J, Wen D, Liu J, Liu S, Huang Z (2007) Litterfall production along successional and altitudinal gradients of subtropical monsoon evergreen broadleaved forests in Guangdong, China. Plant Ecol 188:77–89

    Article  Google Scholar 

Download references

Acknowledgements

This research was supported by the National Natural Science Foundation of China (no. 31570422) and Guangdong Science and Technology Program (no. 2016A030303044). We thank Mr Yiming Fan for field investigation. Thanks are also due to Prof. Bruce Jaffee for English editing and constructive comments and to anonymous reviewers for their valuable comments on an early version of the manuscript.

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Correspondence to Hai Ren.

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Communicated by Shayne Martin Jacobs.

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Appendices

Appendix 1

See Table 3.

Table 3 The species compositions and species important values in the three successional forests

Appendix 2

See Table 4.

Table 4 The defense traits of dominant species in different successional stages of subtropical forests in South China

Appendix 3

See Table 5.

Table 5 The environment factors in the three successional forests in South China (unpublished)

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Han, T., Wang, J., Ren, H. et al. Changes in defense traits of young leaves in subtropical forests succession. Plant Ecol 220, 305–320 (2019). https://doi.org/10.1007/s11258-019-00916-1

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