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Effect of artificially accelerated aging on the vigor of Metasequoia glyptostroboides seeds

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Abstract

Metasequoia glyptostroboides is an endangered relict plant native to China that has been widely introduced into many countries and areas around the world. However, its seeds germinate at a very low percentage. Consequently, population regeneration by seed is low under natural conditions, which probably contributes to the endangered status of this plant species. The present study aimed to describe the aging mechanism of M. glyptostroboides seeds. Our objective was to elucidate causes of the low germination rate in an effort to enhance potential for conservation of the species. We used germination tests, relative electrical conductivity and malondialdehyde content determination, ultrastructural observation of embryo cells, and analysis of superoxide dismutase, catalase, ascorbate peroxidase, and dehydroascorbate reductase activities during accelerated aging treatment. We found that M. glyptostroboides seeds have a low level of vigor and poor ability to maintain vigor, which is probably associated with the inefficiency of its enzymatic antioxidative system.

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Abbreviations

ANOVA:

Analysis of variance

APX:

Ascorbate peroxidase

AsA:

Ascorbate peroxidase

CAT:

Catalase

CM:

Cytoplasmic membrane

CW:

Cell wall

DC:

Druse crystal

DHA:

Dehydroascorbate

DHAR:

Dehydroascorbate reductase

DW:

Dry weight

G:

Glyoxysome

GCC:

Globoid crystal cavity

GR:

Glutathione reductase

GSH:

Glutathione

GSSG:

Oxidized glutathione

H2O2 :

Hydrogen peroxide

IS:

Intercellular space

ISTA:

International rules for seed testing

LB:

Lipid body

MDA:

Malondialdehyde

MDHAR:

Monodehydroascorbate reductase

Mt:

Mitochondrion

N:

Nucleus

\({\text{O}}_{ 2}^{ - }\) :

Superoxide radicals

·OH:

Hydroxy radicals

1O2 :

Singlet oxygen

P:

Probability

PB:

Protein body

PPFD:

Photosynthetic Photon Flux Density

RH:

Relative humidity

ROS:

Reactive oxygen species

S:

Starch granule

SE:

Standard error

SG:

Soft globoid

S–N–K:

Student–Newman–Keuls

SOD:

Superoxide dismutase

References

  • Aebi H (1984) Oxygen radicals in biological systems. Methods Enzymol 105:121–126

    Article  CAS  PubMed  Google Scholar 

  • Asada K, Takahashi M (1987) Production and scavenging of active oxygen in photosynthesis. In: Kyle DJ, Osmond CB, Arntzen CJ (eds) Photoinhibition. Elsevier, Amsterdam, pp 227–287

    Google Scholar 

  • Bailly C (2004) Active oxygen species and antioxidants in seed biology. Seed Sci Res 14:93–107

    Article  CAS  Google Scholar 

  • Bailly C, Benamar A, Corbineau F, Côme D (1996) Changes in malondialdehyde content and superoxide dismutase, catalase and glutathione reductase activities in sunflower seeds as related to deterioration during accelerated aging. Physiol Plantarum 97:104–110

    Article  CAS  Google Scholar 

  • Bailly C, El-Maarouf-Bouteau H, Corbineau F (2008) From intercellular signalling networks to cell death: the dual role of reactive oxygen species in seed physiology. CR Biol 331:806–814

    Article  CAS  Google Scholar 

  • Barreto LC, Garcia QS (2017) Accelerated ageing and subsequent imbibition affect seed viability and the efficiency of antioxidant system in macaw palm seeds. Acta Physiol Plant 39(3):72

    Article  CAS  Google Scholar 

  • Bowler C, Slooten L, Vandenbranden S, De Rycke R, Botterman J, Sybesma C, van Montagu M, Inze D (1991) Manganese superoxide dismutase can reduce cellular damage mediated by oxygen radicals in transgenic plants. EMBO J 10:1723–1732

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Bowler C, Montagu MV, Inze D (1992) Superoxide dismutases and stress tolerance. Annu Rev Plant Physiol Mol Biol 43:83–116

    Article  CAS  Google Scholar 

  • Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254

    Article  CAS  PubMed  Google Scholar 

  • Cao JW, Liu CL, Zhang B, Wu Y, Zhu L, Liu G, Li SC (2010) Seed germination of endangered Cathaya argyrophylla Chun & Kuang. Acta Ecol Sin 30(15):4027–4034 (in Chinese with English abstract)

    CAS  Google Scholar 

  • Dalton DA, Baird LM, Langeberg L, Taugher CY, Anyan WR, Vance CP, Sarath G (1993) Subcellular localization of oxygen defense enzymes in soybean (Glycine max (L.) Merr.) root nodules. Plant Physiol 102:481–489

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Deng ZJ, Cheng HY, Song SQ (2010) Effects of temperature, scarification, dry storage, stratification, phytohormone and light on dormancy-breaking and germination of Cotinus coggygria var. Cinerea (Anacardiaceae) seeds. Seed Sci Technol 38:572–584

    Article  Google Scholar 

  • Donà M, Balestrazzi A, Mondoni A, Rossi G, Ventura L, Buttafava A, Macovei A, Sabatini ME, Valassi A, Carbonera D (2013) DNA profiling, telomere analysis and antioxidant properties as tools for monitoring ex situ seed longevity. Ann Bot 111:987–998

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  • El-Maarouf Bouteau H, Bailly C (2008) Oxidative signaling in seed germination and dormancy. Plant Signal Behav 3:175–182

    Article  PubMed  PubMed Central  Google Scholar 

  • Engelmann F (2000) Importance of cryopreservation for the conservation of plant genetic resources. In: Engelmann F, Takagi H (eds) Cryopreservation of tropical germplasm: current research progress and application. Japan International Research Centre for Agricultural Sciences, Tsukuba, pp 8–20

    Google Scholar 

  • Goel A, Sheoran IS (2003) Lipid peroxidation and peroxide-scavenging enzyme in cotton seeds under natural ageing. Biol Plant 46:429–434

    Article  CAS  Google Scholar 

  • Goel A, Goel AK, Sheoran IS (2003) Changes in oxidative stress enzymes during artificial ageing in cotton (Gossypium hirsutum L.) seeds. J Plant Physiol 160:1093–1100

    Article  CAS  PubMed  Google Scholar 

  • Gove PB (1965) Webster’s seventh new college dictionary. G.&C. Merriam Co, Springfield

    Google Scholar 

  • Hodges DM, DeLong JM, Forney CF, Prange RK (1999) Improving the thiobarbituric acid-reactive-substances assay for estimating lipid peroxidation in plant tissues containing anthocyanin and other interfering compounds. Planta 207:604–611

    Article  CAS  Google Scholar 

  • Hu D, Ma G, Wang Q, Yao J, Wang Y, Pritchard HW, Wang X (2012) Spatial and temporal nature of reactive oxygen species production and programmed cell death in elm (Ulmus pumila L.) seeds during controlled deterioration. Plant Cell Environ 35:2045–2059

    Article  CAS  PubMed  Google Scholar 

  • ISTA (2013) Chapter 9: determination of moisture content. In: ISTA (ed) International rules for seed testing. International Seed Testing Association, Bassersdorf, Zurich

    Google Scholar 

  • Kapoor N, Arya A, Siddiqui MA, Kumar H, Amir A (2011) Physiological and biochemical changes during seed deterioration in aged seeds of Rice. Am J Plant Physiol 6:28–35

    Article  Google Scholar 

  • Kibinza S, Vinel D, Côme D, Bailly C, Corbineau F (2006) Sunflower seed deterioration as related to moisture content during ageing, energy metabolism and active oxygen species scavenging. Physiol Plant 128:496–506

    Article  CAS  Google Scholar 

  • Krainart C, Siri B, Vichitphan K (2015) Effects of accelerated aging and subsequent priming on seed quality and biochemical change of hybrid cucumber (Cucumis sativa Linn.) seeds. Int J Agric Technol 11(1):165–179

    CAS  Google Scholar 

  • Li YY, Tsang EPK, Cui MY, Chen XY (2012) Too early to call it success: an evaluation of the natural regeneration of the endangered Metasequoia glyptostroboides. Biol Conserv 150:1–4

    Article  Google Scholar 

  • Liu X, Xing D, Li L, Zhang L (2007) Rapid deterioration of seed vigour based on the level of superoxide generation during early imbibition. Photochem Photobiol Sci 6:767–774

    Article  CAS  PubMed  Google Scholar 

  • Long RL, Panetta FD, Steadman KJ, Probert R, Bekker R, Brooks S, Adkins SW (2008) Seed persistence in the field may be predicted by laboratory-controlled aging. Weed Sci 56:523–528

    Article  CAS  Google Scholar 

  • Ma J, Shao G (2003) Rediscovery of the “first collection” of the “living fossil”, Metasequoia glyptostroboides. Taxon 52:585–588

    Article  Google Scholar 

  • Ma LY, Wang XQ, Guo BX (2006) Progress on introduction and ex situ conservation on Metasequoia glyptostrobodies in the world. Guihaia 26(3):235–241 (in Chinese with English abstract)

    Google Scholar 

  • Matamoros MA, Loscos J, Coronado MJ, Ramos J, Sato S, Testillano PS, Tabata S, Becana M (2006) Biosynthesis of ascorbic acid in legume root nodules. Plant Physiol 141:1068–1077

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Matamoros MA, Fernández-García N, Wienkoop S, Loscos J, Saiz A, Becana M (2013) Mitochondria are an early target of oxidative modifications in senescing legume nodules. New Phytol 197:873–885

    Article  CAS  PubMed  Google Scholar 

  • Miller G, Shulaev V, Mittler R (2008) Reactive oxygen signalling and abiotic stress. Physiol Plant 133:481–489

    Article  CAS  PubMed  Google Scholar 

  • Mittler R (2002) Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci 7(9):405–410

    Article  CAS  PubMed  Google Scholar 

  • Mittova V, Volokita M, Guy M, Tal M (2000) Activities of SOD and the ascorbate–glutathione cycle enzymes in subcellular compartments in leaves and roots of the cultivated tomato and its wild salt-tolerant relative Lycopersicon pennellii. Physiol Plant 110:42–51

    Article  CAS  Google Scholar 

  • Moore RP (1973) Tetrazolium staining for assessing seed quality. In: Heydecker W (ed) Seed ecology. Butterworths, London, pp 347–366

    Google Scholar 

  • Munné-Bosch S, Oñate M, Oliveira PG, Garcia QS (2011) Changes in phytohormones and oxidative stress markers in buried seeds of Vellozia alata. Flora 206:704–711

    Article  Google Scholar 

  • Nagel M, Borner A (2010) The longevity of crop seeds stored under ambient conditions. Seed Sci Res 20:1–12

    Article  Google Scholar 

  • Nakano Y, Asada K (1981) Hydrogen peroxide scavenged by ascorbate-specific peroxidase in spinach chloroplast. Plant Cell Physiol 22:867–880

    CAS  Google Scholar 

  • Negreiros GF, Perez SCJG (2004) Physiological response of palm seeds to accelerated aging. Pesqui Agropecu Bras 39(4):391–396 (in Portuguese with English abstract)

    Article  Google Scholar 

  • Olofinboba MO, Kozlowski TT (1982) Effects of three systemic insecticides on seed germination and growth of Pinus halepensis seedlings. Plant Soil 64:255–258

    Article  CAS  Google Scholar 

  • Rajjou L, Lovigny Y, Groot SPC, Belghazi M, Job C, Job D (2008) Proteome-wide characterization of seed aging in Arabidopsis: a comparison between artificial and natural aging protocols. Plant Physiol 148:620–641

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Rao KVM, Sresty TVS (2000) Antioxidant parameters in the seedlings of pigeon pea (Cajanus cajan (L.) Millspaugh) in response to Zn and Ni stresses. Plant Sci 157:113–128

    Article  Google Scholar 

  • Sano N, Rajjou L, North HM, Debeaujon I, MarionPoll A, Seo M (2016) Staying alive: molecular aspects of seed longevity. Plant Cell Physiol 57(4):660

    Article  CAS  PubMed  Google Scholar 

  • Sarvajeet SG, Narendra T (2010) Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol Biochem 48:909–930

    Article  CAS  Google Scholar 

  • Satoh K (1999) Metaseguoia travels the globe. Arnold 58/59(4/1):72–75

    Google Scholar 

  • Shaban M (2013) Review on physiological aspects of seed deterioration. Int J Agric Crop Sci 6:627–631

    CAS  Google Scholar 

  • Sharma P, Jha AB, Dubey RS, Pessarakli M (2012) Reactive oxygen species, oxidative damage, and antioxidative defense mechanism in plants under stressful conditions. J Bot 20:121–126

    Google Scholar 

  • Sidari M, Mallamaci C, Muscolo A (2008) Drought, salinity and heat differently affect seed germination of Pinus pinea. J For Res 13:326–330

    Article  CAS  Google Scholar 

  • Smirnoff N (1993) The role of active oxygen in the response of plants to water deficit and desiccation. New Phytol 125:27–58

    Article  CAS  PubMed  Google Scholar 

  • Sung JM (1996) Lipid peroxidation and peroxide-scavenging in soybean seeds during aging. Physiol Plant 97:85–89

    Article  CAS  Google Scholar 

  • Walters C, Wheeler LM, Stanwood PC (2004) Longevity of cryogenically stored seeds. Cryobiology 48:229–244

    Article  PubMed  Google Scholar 

  • Wang XQ, Ma LY, Guo BX (2004) History and research progress on the silviculture of Metasequoia glyptostroboides in China. J Northwest For Univ 19(2):82–88 (in Chinese with English abstract)

    CAS  Google Scholar 

  • Wang JS, Zheng WL, Pan G (2005) Relation between being endangered and seed vigor about Cupressus gigantea in Tibet. Sci Silvae Sin 41(4):37–41 (in Chinese with English abstraction)

    Google Scholar 

  • Wang Y, Li Y, Xue H, Pritchard HW, Wang XF (2015) Reactive oxygen species-provoked mitochondria-dependent cell death during ageing of elm (Ulmus pumila L.) seeds. Plant J 81:438–452

    Article  CAS  PubMed  Google Scholar 

  • Wen JJ, Wu B, Li YL, Fan SH (2001) Status and problems in the conservation of old Metasequoia glyptostroboides trees. For Sci Technol 3:30–31 (in Chinese)

    Google Scholar 

  • Willekens H, Chamnongpol S, Davey M, Schraudner M, Langebartels C, Montagu MV, Inzé D, Camp WV (1997) Catalase is a sink for H2O2 and is indispensable for stress defence in C3 plants. EMBO J 16:4806–4816

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Xia FS, Chen LL, Sun Y, Mao PS (2015) Relationships between ultrastructure of embryo cells and biochemical variations during ageing of oat (Avena sativa L.) seeds with different moisture content. Acta Physiol Plant 37:89

    Article  CAS  Google Scholar 

  • Xin X, Jing XM, Sun HM, Lin J, Wang XF (2004) Ecophysiological characteristics of seed germination of the relict plant Metasequoia glyptostroboides. Biodiv Sci 12(6):572–577 (in Chinese with English abstract)

    Google Scholar 

  • Xin X, Tian Q, Yin GK, Chen XL, Zhang JM, Ng S, Lu XY (2014) Reduced mitochondrial and ascorbate–glutathione activity after artificial ageing in soybean seed. J Plant Physiol 171:140–147

    Article  CAS  PubMed  Google Scholar 

  • Yang H (1998-1999) From fossils to molecules: the Metasequoia tale continues. Arnoldia 58/59(4/1):60–71

  • Yao Z, Liu LW, Gao F, Rampitsch C, Reinecke DM, Ozga JA, Ayele BT (2012) Developmental and seed aging mediated regulation of antioxidative genes and differential expression of proteins during pre- and post-germinative phases in pea. Plant Physiol 169:1477–1488

    Article  CAS  Google Scholar 

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Acknowledgements

This work was supported by the Research Project of Hubei Provincial Department of Education (Q20141902). We thank LetPub (www.letpub.com) for providing linguistic assistance during the preparation of this manuscript.

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Correspondence to Zhijun Deng.

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The authors declare that they have no conflict of interest. Huan Liu and Yanfang Zhu contributed equally to this work.

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Project funding: This work was supported by the Research Project of Hubei Provincial Department of Education (Q20141902).

The online version is available at http://www.springerlink.com

Corresponding editor: Zhu Hong.

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Liu, H., Zhu, Y., Liu, X. et al. Effect of artificially accelerated aging on the vigor of Metasequoia glyptostroboides seeds. J. For. Res. 31, 769–779 (2020). https://doi.org/10.1007/s11676-018-0840-1

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  • DOI: https://doi.org/10.1007/s11676-018-0840-1

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