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Waterlogging under simulated late-winter conditions had little impact on the physiology and growth of Norway spruce seedlings

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Abstract

Context

Waterlogging is predicted to become more common in boreal forests during winter and early spring with climate change. So far, little is known about the waterlogging tolerance of boreal tree species during their winter dormancy.

Aim

The aim was to quantify the degree of waterlogging tolerance of 1-year-old dormant Norway spruce (Picea abies (L.) Karst.) seedlings.

Methods

The seedlings were exposed to waterlogging in a growth chamber at temperature of 2 °C for 4 weeks and then allowed to recover for 6 weeks during the growth stage. Shoot and root responses were monitored by physiological and growth measurements.

Results

No effect was found in the seedling biomass, but root mortality increased slightly during the early growth stage following waterlogging. The water potential of the needles became less negative at the end of the waterlogging and the early growth stage. The ratio of apoplastic to symplastic electrical resistance (R e/R i) of the needles was lower after waterlogging, indicating changes in the proportions of symplastic and apoplastic space. No differences were found between the treatments in the dark-acclimated chlorophyll fluorescence (F v/F m) of the needles. Slightly greater accumulation of starch and temporary reductions of some mineral nutrients in needles were found after waterlogging.

Conclusions

We conclude that in late winter and early spring, Norway spruce seedlings potentially tolerate short periods of waterlogging.

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References

  • Adams MB, Allen HL, Davey CB (1986) Accumulation of starch in roots and foliage of loblolly pine (Pinus taeda L.): Effects of season, site and fertilization. Tree Phys 2:35–46

    Article  CAS  Google Scholar 

  • Armstrong W, Read DJ (1972) Some observations on oxygen transport in conifer seedlings. New Phytol 71:55–62

    Article  Google Scholar 

  • Aroca R, Porcel R, Ruiz-Lozano JM (2012) Regulation of root water uptake under abiotic stress conditions. J Exp Bot 63:43–57

    Article  PubMed  CAS  Google Scholar 

  • Aronen TS, Häggman HM (1994) Occurrence of lenticels in roots of Scots pine seedlings in different growth conditions. J Plant Physiol 143:325–329

    Article  Google Scholar 

  • Baker NR (2008) Chlorophyll fluorescence: a probe of photosynthesis in vivo. Ann Rev Plant Biol 59:89–113

    Article  CAS  Google Scholar 

  • Bardossy A, Caspary HJ (1990) Detection of climate change in Europe by analyzing European atmospheric circulation patterns from 1881 to 1989. Theor Appl Climatol 42:155–167

    Article  Google Scholar 

  • Brahim MB, Loustau D, Gaudillère JP, Saur E (1996) Effects of phosphate deficiency on photosynthesis and accumulation of starch and soluble sugars in 1-year-old seedlings of maritime pine (Pinus pinaster Ait). Ann Sci For 53:801–810

    Article  Google Scholar 

  • Calvo-Polanco M, Señorans J, Zwiazek JJ (2012) Role of adventitious roots in water relations of tamarack (Larix laricina) seedlings exposed to flooding. BMC Plant Biol 12:99–107

    Article  PubMed  CAS  Google Scholar 

  • Calvo-Polanco M, Zwiazek JJ, Jones MD, MacKinnon MD (2009) Effects of NaCl on responses of ectomycorrhizal black spruce (Picea mariana), white spruce (Picea glauca) and jack pine (Pinus banksiana) to fluoride. Physiol Plant 135:51–61

    Article  PubMed  CAS  Google Scholar 

  • Chow PS, Landhäusser SM (2004) A method for routine measurements of total sugar and starch content in woody plant tissues. Tree Phys 24:1129–1136

    Article  CAS  Google Scholar 

  • Conlin TSS, Lieffers VJ (1993) Anaerobic and aerobic CO2 efflux rates from boreal forest conifer roots at low temperatures. Can J For Res 23:767–771

    Article  CAS  Google Scholar 

  • Coutts MP, Nicoll BC (1990) Waterlogging tolerance of roots of Sitka spruce clones and of strands from Thelephora terrestris mycorrhizas. Can J For Res 20:1894–1899

    Article  Google Scholar 

  • Coutts MP, Philipson JJ (1978) Tolerance of tree roots to waterlogging. I. Survival of Sitka spruce and Lodgepole pine. New Phytol 80:63–69

    Article  Google Scholar 

  • Crawford RMM (2003) Seasonal differences in plant responses to flooding and anoxia. Can J Bot 81:1224–1246

    Article  CAS  Google Scholar 

  • Crawford RMM, Braendle R (1996) Oxygen deprivation stress in a changing environment. J Exp Bot 47:145–159

    Article  CAS  Google Scholar 

  • Glenz C, Schlaepfer R, Iorgulescu I, Kienast F (2006) Flooding tolerance of Central European tree and shrub species. Ecol Manag 235:1–13

    Article  Google Scholar 

  • Gourzi A, Rouane A, Alavi SM, McHugh MB, Nadi M, Roth P, Poincare H (2004) Body fluid characterization using a new electromagnetic biosensor: blood PIG in vitro results. In: Nowakowski A, Wtorek J, Bujnowski A, Janczulewicz A (eds.), Proc 7th Int Conf Electr Bioimp & 5th Electr Imp Tomography 1: 241–244

  • Hansen J, Møller I (1975) Percolation of starch and soluble carbohydrates from plant tissue for quantitative determination with anthrone. Anal Biochem 68:87–94

    Article  PubMed  CAS  Google Scholar 

  • IPCC (2007) Climate change 2007: the physical science basis. In: Solomon S, Qin D, Manning M, Chen Z, Marquis M, Averyt KB, Tignor M, Miller HL (eds) Contribution of Working Group I to the Fourth Assessment Report of the Intergovernmental Panel on Climate Change. Cambridge University Press, Cambridge, p 940

    Google Scholar 

  • Islam A, Macdonald SE, Zwiazek JJ (2003) Responses of black spruce (Picea mariana) and tamarack (Larix laricina) to flooding and ethylene treatments. Tree Physiol 23:535–542

    Article  Google Scholar 

  • Jylhä K, Ruosteenoja K, Räisänen J, Venäläinen A, Tuomenvirta H, Ruokolainen L, Saku S, Seitola T (2009) The changing climate in Finland: estimates for adaptation studies. ACCLIM project report 2009. Finn Meteorol Inst Helsinki, Reports 2009: 4, 102 p. Extended abstract in English

  • Kamaluddin M, Zwiazek JJ (2002) Ethylene enhances water transport in hypoxic aspen (Populus tremuloides). Plant Physiol 128:962–969

    Article  PubMed  CAS  Google Scholar 

  • Knipfer T, Das D, Steudle E (2007) During measurements of root hydraulics with pressure probes, the contribution of unstirred layers is minimized in the pressure relaxation mode: comparison with pressure clamp and high-pressure flowmeter. Plant Cell Environ 30:845–860

    Article  PubMed  Google Scholar 

  • Kortelainen P, Saukkonen S (1995) Organic vs minerogenic acidity in headwater streams in Finland. Water Air Soil Pollut 85:559–564

    Article  CAS  Google Scholar 

  • Kozlowski TT (1997) Responses of woody plants to flooding and salinity. Tree Physiol Monogr 1:1–29

    Google Scholar 

  • Kreuzwieser J, Gessler A (2010) Global climate change and tree nutrition: influence of water availability. Tree Physiol 30:1221–1234

    Article  PubMed  CAS  Google Scholar 

  • Kreuzwieser J, Papadopoulou E, Rennenberg H (2004) Interaction of flooding with carbon metabolism of forest trees. Plant Biol 6:299–306

    Article  PubMed  CAS  Google Scholar 

  • Lichtenthaler HK, Rinderle U (1988) The role of chlorophyll fluorescence in the detection of stress conditions in plants. Crit Rev Anal Chem 19:29–85

    Google Scholar 

  • Palomäki V, Holopainen JK, Holopainen T (1994) Effects of drought and waterlogging on ultrastructure of Scots pine and Norway spruce needles. Trees 9:98–105

    Article  Google Scholar 

  • Parent C, Capelli N, Berger A, Crèvecoeur M, Dat JF (2008) An overview of plant responses to soil waterlogging. Plant Stress 2:20–27

    Google Scholar 

  • Pelkonen E (1975) Effects on Scots pine growth of ground water adjusted to the ground surface for periods of varying length during different seasons of the year. Suo 26:25–32

    Google Scholar 

  • Pelkonen E (1979) Seasonal flood tolerance of Scots pine and Norway spruce seedlings. Suo 30:35–42

    Google Scholar 

  • Pereira JS, Kozlowski TT (1977) Variations among woody angiosperms in response to flooding. Physiol Plant 41:184–192

    Article  Google Scholar 

  • Puhe J (2003) Growth and development of the root system of Norway spruce in forest stands—a review. Ecol Manag 175:253–273

    Article  Google Scholar 

  • Racey GD (1984) Dissolved oxygen depletion by the roots of conifer seedlings during root soaking. Ont Min Nat Resour Res Notes 41:1–4

    Google Scholar 

  • Reece CF, Riha SJ (1991) Role of root systems of eastern larch and white spruce in response to flooding. Plant Cell Environ 14:229–234

    Article  Google Scholar 

  • Repo T, Zhang G, Ryyppö A, Rikala R (2000) Electrical impedance spectroscopy of Scots pine (Pinus sylvestris L.) shoots in relation to cold acclimation. J Exp Bot 51:2095–2107

    Article  PubMed  CAS  Google Scholar 

  • Repo T, Zhang MIN, Ryyppö A, Vapaavuori E, Sutinen S (1994) Effects of freeze–thaw injury on parameters of distributed electrical circuits of stems and needles of Scots pine seedlings at different stages of acclimation. J Exp Bot 45:823–833

    Article  Google Scholar 

  • Ryyppö A, Repo T, Vapaavuori E (1998) Development of freezing tolerance in roots and shoots of Scots pine seedlings at non-freezing temperatures. Can J For Res 28:557–567

    Article  Google Scholar 

  • Sallantaus T (1992) Leaching in the material balance of peatlands—preliminary results. Suo 43:253–258

    Google Scholar 

  • Sarkkola S, Hökkä H, Ahti E, Koivusalo H, Nieminen M (2012) Depth of water table prior to ditch network maintenance is a key factor for tree growth response. Scand J For Res 27:649–658

    Article  Google Scholar 

  • Scholander PF, Hammel HT, Hemmingsen EA, Bradstreet ED (1964) Hydrostatic pressure and osmotic potential in leaves of mangroves and some other plants. Proc Natl Acad Sci U S A 52:119–125

    Article  PubMed  CAS  Google Scholar 

  • Sudachkova NE, Milyutina IL, Romanova LI (2009) Adaptive responses of Scots pine to the impact of adverse abiotic factors on the rhizosphere. Russ J Ecol 40:387–392

    Article  Google Scholar 

  • Terazawa K, Maruyama Y, Morikawa Y (1992) Photosynthetic and stomatal responses of Larix kaempferi seedlings to short-term waterlogging. Ecol Res 7:193–197

    Article  Google Scholar 

  • Topa MA, Cheeseman JM (1992a) Effects of root hypoxia and a low P supply on relative growth, carbon dioxide exchange rates and carbon partitioning in Pinus serotina seedlings. Phys Plant 86:136–144

    Article  CAS  Google Scholar 

  • Topa MA, Cheeseman JM (1992b) Carbon and phosphorus partitioning in Pinus serotina seedlings growing under hypoxic and low-P conditions. Tree Phys 10:195–207

    Article  CAS  Google Scholar 

  • Tournaire-Roux C, Sutka M, Javot H, Gout E, Gerbeau P, Luu DT, Bligny R, Maurel C (2003) Cytosolic pH regulates root water transport during anoxic stress through gating of aquaporins. Nature 425:393–397

    Article  PubMed  CAS  Google Scholar 

  • Tyree MT, Patiño S, Bennink J, Alexander J (1995) Dynamic measurements of root hydraulic conductance using a high–pressure flowmeter in the laboratory and field. J Exp Bot 46:83–94

    Article  CAS  Google Scholar 

  • Utriainen J, Holopainen T (2001) Nitrogen availability modifies the ozone responses of Scots pine seedlings exposed in an open-field system. Tree Physiol 21:1205–1213

    Article  PubMed  CAS  Google Scholar 

  • Zhang MIN, Repo T, Willison JHM, Sutinen S (1995) Electrical impedance analysis in plant tissues: On the biological meaning of Cole-Cole α in Scots pine needles. Eur Biophys J 24:99–106

    Article  Google Scholar 

  • Zhang MIN, Willison JHM, Cox MA, Hall SA (1993) Measurement of heat injury in plant tissue by electrical impedance analysis. Can J Bot 71:1605–1611

    Article  Google Scholar 

Download references

Acknowledgments

We thank Eija Koljonen, Anita Pussinen, Urho Kettunen, Jussi Liinamo, and Jukka-Pekka Lappalainen for their technical assistance, Jaakko Heinonen for his advice on the statistical analyses, Sirkka Sutinen and Gang Zhang for their comments on the manuscript, and Pekka Hirvonen for revising the English text. The study was financed by the Academy of Finland (project 127924), the Finnish Forest Research Institute (project 3489), the Finnish network ‘Doctoral Programme in Forest Sciences’ and the Niemi Foundation.

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Correspondence to Tapani Repo.

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Handling Editor: Erwin Dreyer

Contribution of the co-authors Wang, Roitto, Lehto and Repo designed the experiment. Wang was responsible for running the experiment, analysis of the results, and majority of the writing. All the authors have contributed in preparing of the manuscript.

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Wang, AF., Roitto, M., Lehto, T. et al. Waterlogging under simulated late-winter conditions had little impact on the physiology and growth of Norway spruce seedlings. Annals of Forest Science 70, 781–790 (2013). https://doi.org/10.1007/s13595-013-0325-5

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