Journal of Wood Science

, Volume 64, Issue 1, pp 1–5 | Cite as

Wood structure of Populus alba formed in a shortened annual cycle system

Original Article

Abstract

Wood formation of trees that grow along the seasons has an annual rhythm. Due to this rhythm, physiological research on the mechanism of wood formation has been difficult to conduct in a typical experimental room. In the present study, we observed the wood tissue formation in a shortened annual cycle system, which was developed for poplar trees grown in a growth chamber with dormant and non-dormant cycles. Poplar trees were grown in this system by repeating the cycle three times. The resulting wood tissue consisted of three growth rings and very similar structures were observed around the ring boundary of the wood in a field-grown stem. This result suggests that the shortened annual cycle system can be adopted as a model for physiological, cell biological and molecular research of wood and annual ring formation.

Keywords

Annual cycle Annual ring Wood formation Dormancy Poplar (Populus alba

Notes

Acknowledgements

This work was supported by the Research Institute for Sustainable Humanosphere, Kyoto University (Mission-1). We would like to thank Editage (http://www.editage.jp) for English language editing.

References

  1. 1.
    Keskitalo J, Bergquist G, Gardeström P, Jansson S (2005) A cellular timetable of autumn senescence. Plant Physiol 139:1635–1648CrossRefPubMedPubMedCentralGoogle Scholar
  2. 2.
    van der Schoot C, Rinne PLH (2011) Dormancy cycling at the shoot apical meristem: transitioning between self-organization and self-arrest. Plant Sci 180:120–131CrossRefPubMedGoogle Scholar
  3. 3.
    Rinne P, Saarelainen A, Junttila O (1994) Growth cessation and bud dormancy in relation to ABA level in seedling and coppice shoots of Betula pubescens as affected by a short photoperiod, water stress and chilling. Physiol Plant 90:451–458CrossRefGoogle Scholar
  4. 4.
    Ruttink T, Arend M, Morreel K, Storme V, Rombauts S, Fromm J, Bhalerao RP, Boerjan W, Rohdea A (2007) A molecular timetable for apical bud formation and dormancy induction in poplar. Plant Cell 19:2370–2390CrossRefPubMedPubMedCentralGoogle Scholar
  5. 5.
    Rinne PLH, Paul LK, Vahala J, Ruonala R, Kangasjärvi J, van der Schoot C (2015) Long and short photoperiod buds in hybrid aspen share structural development and expression patterns of marker genes. J Exp Bot 66:6745–6760CrossRefPubMedPubMedCentralGoogle Scholar
  6. 6.
    Howe GT, Gardner G, Hackett WP, Furnier GR (1996) Phytochrome control of short-day-induced bud set in black cottonwood. Physiol Plant 97:95–103CrossRefGoogle Scholar
  7. 7.
    Wake CMF, Fennell A (2000) Morphological, physiological and dormancy responses of three Vitis genotypes to short photoperiod. Physiol Plant 109:203–210CrossRefGoogle Scholar
  8. 8.
    Pagter M, Liu F, Jensen CR, Petersen KK (2008) Effects of chilling temperatures and short photoperiod on PSII function, sugar concentrations and xylem sap ABA concentrations in two Hydrangea species. Plant Sci 175:547–555CrossRefGoogle Scholar
  9. 9.
    Welling A, Kaikuranta P, Rinne P (1997) Photoperiodic induction of dormancy and freezing tolerance in Betula pubescens. Involvement of ABA and dehydrins. Physiol Plant 100:119–125CrossRefGoogle Scholar
  10. 10.
    Welling A, Moritz T, Palva ET, Junttila O (2002) Independent activation of cold acclimation by low temperature and short photoperiod in hybrid aspen. Plant Physiol 129:1633–1641CrossRefPubMedPubMedCentralGoogle Scholar
  11. 11.
    Heide OM (1974) Growth and dormancy in Norway spruce ecotype (Picea abies) I. Interaction of photoperiod and temperature. Phyiol Plant 30:1–12CrossRefGoogle Scholar
  12. 12.
    Olsen JE, Junttila O, Moritz T (1997) Long-day induced bud break in Salix pentandra is associated with transiently elevated levels of GA1 and gradual increase in indole-3-acetic acid. Plant Cell Physiol 38:536–540CrossRefGoogle Scholar
  13. 13.
    Azeez A, Miskolczi P, Tylewicz S, Bhalerao RPA (2014) Tree ortholog of APETALA1 mediates photoperiodic control of seasonal growth. Curr Biol 24:717–724CrossRefPubMedGoogle Scholar
  14. 14.
    Böhlenius H, Huang T, Charbonnel-Cambaa L, Brunner A, Jansson S, Strauss S, Nilsson O (2006) CO/FT regulatory module controls timing of flowering and seasonal growth cessation in trees. Science 312:1040–1043CrossRefPubMedGoogle Scholar
  15. 15.
    Meilerowicz EJ, Riding RT, Little CHA (1992) Periodicity of cambial activity in Abies balsamea. II. Effects of temperature and photoperiod on the size of the nuclear genome in fusiform cambial cells. Physiol Plant 85:526–530CrossRefGoogle Scholar
  16. 16.
    Zhu B, Coleman GD (2001) Phytochrome-mediated photoperiod perception, shoot growth, glutamine, calcium, and protein phosphorylation influence the activity of the poplar bark storage protein gene promoter (bspA). Plant Physiol 126:342–351CrossRefPubMedPubMedCentralGoogle Scholar
  17. 17.
    Noda Y, Furukawa J, Aohara T, Nihei N, Hirose A, Tanoi K, Nakanishi TM, Satoh S (2016) Short day length-induced decrease of cesium uptake without altering potassium uptake manner in poplar. Sci Rep 6:38360CrossRefPubMedPubMedCentralGoogle Scholar
  18. 18.
    Aohara T, Mizuno H, Kiyomichi D, Abe Y, Matsuki K, Sagawa K, Mori H, Iwai H, Furukawa J, Satoh S (2016) Identification of a xylem sap germin-like protein and its expression under short-day and non-freezing low temperature conditions in poplar root. Plant Biotech 33:123–127CrossRefGoogle Scholar
  19. 19.
    Kurita Y, Baba K, Ohnishi M, Anegawa A, Shichijo C, Kosuge K, Fukaki H, Mimura T (2014) Establishment of a shortened annual cycle system; a tool for the analysis of annual re-translocation of phosphorus in the deciduous woody plant (Populus alba L.). J Plant Res 127:545–551CrossRefPubMedGoogle Scholar
  20. 20.
    Chaffey N (2002) Why is there so little research into the cell biology of the secondary vascular system of trees? New Phytol 153:213–223CrossRefGoogle Scholar
  21. 21.
    Kaku T, Baba K, Tanigchi T, Kurita M, Konagaya K, Ishii K, Kondo T, Serada S, Iizuka H, Kaida R, Taji T, Sakata Y, Hayashi T (2012) Analyses of leaves from open field-grown transgenic poplars overexpressing xyloglucanase. J Wood Sci 58:281–289CrossRefGoogle Scholar
  22. 22.
    Park YW, Baba K, Furuta Y, Kojiro K, Yoshida M, Hayashi T (2010) Characterization of poplar overexpressing xylanase. Wood Res J 1:50–55Google Scholar
  23. 23.
    Kaida R, Kaku T, Baba K, Sri H, Enny S, Hayashi T (2009) Enhancement of saccharification by overexpression of poplar cellulase in sengon. J Wood Sci 55:435–440CrossRefGoogle Scholar
  24. 24.
    Kaku T, Serada S, Baba K, Tanaka F, Hayashi T (2009) Proteomic analysis of the G-layer in poplar tension wood. J Wood Sci 55:250–257CrossRefGoogle Scholar
  25. 25.
    Baba K, Park YW, Kaku T, Kaida R, Takeuchi M, Yoshida M, Hosoo Y, Ojio Y, Okuyama T, Taniguchi T, Ohmiya Y, Kondo T, Shani Z, Shoseyov O, Awano T, Serada S, Norioka N, Norioka S, Hayashi T (2009) Xyloglucan for generating tensile stress to bend tree stem. Mol Plant 2:893–903CrossRefPubMedGoogle Scholar
  26. 26.
    Kaida R, Kaku T, Baba K, Oyadomari M, Watanabe T, Nisida K, Kanaya T, Shani Z, Shoseyov O, Hayash T (2009) Loosening xyloglucan accelerates the enzymatic degradation of cellulose in wood. Mol Plant 2:904–909CrossRefPubMedGoogle Scholar
  27. 27.
    Park YW, Baba K, Furuta Y, Iida I, Sameshima K, Arai M, Hayashi T (2004) Enhancement of growth and cellulose accumulation by overexpression of xyloglucanase in poplar. FEBS Lett 564:183–187CrossRefPubMedGoogle Scholar
  28. 28.
    Baba K, Kurita Y, Mimura T (2017) Architectural morphogenesis of poplar grown in a shortened annual cycle system. Sustain Humanosphere 13 (in print)Google Scholar
  29. 29.
    Kudo K, Yasue K, Hosoo Y, Funada R (2015) Relationship between formation of earlywood vessels and leaf phenology in two ring-porous hardwoods, Quercus serrata and Robinia pseudoacacia, in early spring. J Wood Sci 61:455–464CrossRefGoogle Scholar
  30. 30.
    Takahashi S, Okada N, Nobuchi T (2013) Relationship between the timing of vessel formation and leaf phenology in ten ring-porous and diffuse-porous deciduous tree species. Ecol Res 28:615–624CrossRefGoogle Scholar
  31. 31.
    Takahashi S, Okada N, Nobuchi T (2014) Relationship between vessel porosity and leaf emergence pattern in ring- and diffuse-porous deciduous trees in a temperate hardwood forest. Botany 93:31–39CrossRefGoogle Scholar
  32. 32.
    Kitin P, Funada R (2016) Earlywood vessels in ring-porous trees become functional for water transport after bud burst and before the maturation of the current-year leaves. IAWA J 37:315–331CrossRefGoogle Scholar
  33. 33.
    Kudo K, Nabeshima E, Begum S, Yamagishi Y, Nakaba S, Oribe Y, Yasue K, Funada R (2014) The effects of localized heating and disbudding on cambial reactivation and formation of earlywood vessels in seedlings of the deciduous ring-porous hardwood, Quercus serrata. Ann Bot 113:1021–1027CrossRefPubMedPubMedCentralGoogle Scholar
  34. 34.
    Oribe Y, Kubo T (1997) Effect of heat on cambial reactivation during winter dormancy in evergreen and deciduous conifers. Tree Physiol 17:81–87CrossRefPubMedGoogle Scholar
  35. 35.
    Begum S, Nakaba S, Yamagishi Y, Oribe Y, Funada R (2013) Regulation of cambial activity in relation to environmental conditions: understanding the role of temperature in wood formation of trees. Physiol Plant 147:46–54CrossRefPubMedGoogle Scholar
  36. 36.
    Begum S, Kudo K, Matsuoka Y, Nakaba S, Yamagishi Y, Nabeshima E, Rahman MH, Nugroho WD, Oribe Y, Jin H-O, Funada R (2016) Localized cooling of stems induces latewood formation and cambial dormancy during seasons of active cambium in conifers. Ann Bot 117:465–477CrossRefPubMedGoogle Scholar

Copyright information

© The Japan Wood Research Society 2017

Authors and Affiliations

  1. 1.Research Institute for Sustainable HumanosphereKyoto UniversityUjiJapan
  2. 2.Graduate School of ScienceKobe UniversityKobeJapan
  3. 3.Faculty of AgricultureRyukoku UniversityOtsuJapan

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