Direct exposure to solar radiation causes radial growth eccentricity at the beginning of the growing season in Robinia pseudoacacia
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Abstract
Our study investigated the effect of stem temperature increase on xylem formation in Robinia pseudoacacia tree-trunks, caused by direct exposure to solar radiation. It is important to determine factors which may improve the concentricity of deposited wood tissue and intensify xylogenesis because a strong irregularity of wood tissue deposited in the radial direction in mature trees of R. pseudoacacia reduces the commercial value of the wood. Samples of vascular cambium along with adjacent tissues were collected from the southern (illuminated) and northern (shaded) side of tree-trunks growing in the inner and peripheral (thus exposed to direct sunlight) zones of the research plot. Sampling was performed several times during the growing season. The collected material was examined by epifluorescence microscopy and the thickness of deposited tissue comprising cambial xylem derivatives was measured. Deposition of a markedly greater amount of xylem on the southern side of tree-trunks in the peripheral zone of the plot was observed before full leaf development. Instrumental climatic data confirmed that in the early stage of the growing season, temperature on the southern side of the peripheral zone tree-trunk was higher than on the northern side. No clear response in terms of directional deposition of xylem was noticed in the inner zone trees and in peripheral zone trees after full leaf development. This study highlights the importance of temperature increase, caused by solar radiation, for R. pseudoacacia xylogenesis, which may be considered as a factor that affects the course of the radial growth before full leaf development.
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-
Aiso H, Kezuka S, Hiraiwa T, Ishiguri F, Yokota S. 2017. Effects of different inclination angle of stems on anatomical and chemical characteristics of tension wood in Cercidiphyllum japonicum Sieb. et Zucc. Bull. Utsunomiya Univ. For. 53: 55–60.
-
Akaike H. 1974. A new look at the statistical model identification. IEEE Trans. Automat. Contr. 19: 716–723. DOI: 10.1109/TAC.1974.1100705.
-
Alexandre J, Lassalles J-P. 1991. Hydrostatic and osmotic pressure activated channel in plant vacuole. Biophys. J. 60: 1326–1336. DOI: 10.1016/S0006-3495(91)82170-1.
-
Alméras T, Yoshida M, Okuyama T. 2006. Strains inside xylem and inner bark of a stem submitted to a change in hydrostatic pressure. Trees 20: 460–467. DOI: 10.1007/s00468-006-0061-7.
-
Aloni R. 2013. Role of hormones in controlling vascular differentiation and the mechanism of lateral root initiation. Planta 238: 819–830. DOI: 10.1007/s00425-013-1927-8.
-
Aloni R, Peterson CA. 1997. Auxin promotes dormancy callose removal from the phloem of Magnolia kobus and callose accumulation and earlywood vessel differentiation in Quercus robur. J. Plant Res. 110: 37–44. DOI: 10.1007/BF02506841.
-
Barnett JR, Miller H. 1994. The effect of applied heat on graft union formation in dormant Picea sitchensis (Bong.) Carr. J. Exp. Bot. 45: 135–143. DOI: 10.1093/jxb/45.1.135.
-
Barrett RP, Mebrahtu T, Hanover JW. 1990. Black locust: a multi-purpose tree species for temperate climates. In: Janick J, Simon JE (eds.), Advances in new crops: 278–283. Timber Press, Portland, OR.
-
Begum S, Nakaba S, Oribe Y, Kubo T, Funada R. 2007. Induction of cambial reactivation by localized heating in a deciduous hardwood hybrid poplar (Populus sieboldii × P. grandidentata). Ann. Bot. 100: 439–447. DOI: 10.1093/aob/mcm130.
-
Begum S, Nakaba S, Yamagishi Y, Yamane K, Islam MdA, Oribe Y, Ko J-H, Jin H-O, Funada R. 2012. A rapid decrease in temperature induces latewood formation in artificially reactivated cambium of conifer stems. Ann. Bot. 110: 875–885. DOI: 10.1093/aob/mcs149.
-
Cosgrove DJ. 2018. Diffuse growth of plant cell walls. Plant Physiol. 176: 16–27. DOI: 10.1104/pp.17.01541.
-
Dhonukshe P, Aniento F, Hwang I, Robinson DG, Mravec J, Stierhof Y-D, Friml J. 2007. Clathrin-mediated constitutive endocytosis of PIN auxin efflux carriers in Arabidopsis. Curr. Biol. 17: 520–527. DOI: 10.1016/j.cub.2007.01.052.
-
Digby J, Wareing PF. 1966. The relationship between endogenous hormone levels in the plant and seasonal aspects of cambial activity. Ann. Bot. 30: 607–622. DOI: 10.1093/oxfordjournals.aob.a084100.
-
Felix G, Regenass M, Boller T. 2000. Sensing of osmotic pressure changes in tomato cells. Plant Physiol. 124: 1169–1179. DOI: 10.1104/pp.124.3.1169.
-
Frankenstein C, Eckstein D, Schmitt U. 2005. The onset of cambium activity — a matter of agreement? Dendrochronologia 23: 57–62. DOI: 10.1016/j.dendro.2005.07.007.
-
Frankenstein C, Schmitt U. 2006. Microscopic studies on modified wall structure and lignin topochemistry in xylem fibres of poplar after wounding. Maderas, Cienc. Tecnol. 8: 93–106. DOI: 10.4067/S0718-221X2006000200003.
-
Franklin KA, Lee SH, Patel D, Kumar SV, Spartz AK, Gu C, Ye S, Yu P, Breen G, Cohen JD, Wigge PA, Gray WM. 2011. PHYTOCHROME-INTERACTING FACTOR 4 (PIF4) regulates auxin biosynthesis at high temperature. Proc. Natl. Acad. Sci. U.S.A. 108: 20231–20235. DOI: 10.1073/pnas.1110682108.
-
Gray WM, Östin A, Sandberg G, Romano CP, Estelle M. 1998. High temperature promotes auxin-mediated hypocotyl elongation in Arabidopsis. Proc. Natl. Acad. Sci. U.S.A. 95: 7197–7202. DOI: 10.1073/pnas.95.12.7197.
-
Gričar J, Zupančič M, Čufar K, Koch G, Schmitt U, Oven P. 2006. Effect of local heating and cooling on cambial activity and cell differentiation in the stem of Norway spruce (Picea abies). Ann. Bot. 97: 943–951. DOI: 10.1093/aob/mcl050.
-
Groover A. 2016. Gravitropisms and reaction woods of forest trees — evolution, functions and mechanisms. New Phytol. 211: 790–802. DOI: 10.1111/nph.13968.
-
Hager A, Menzel H, Krauss A. 1971. Versuche und Hypothese zur Primärwirkung des Auxins beim Streckungswachstum. Planta 100: 47–75. DOI: 10.1007/BF00386886.
-
Hamann T, Bennett M, Mansfield J, Somerville C. 2009. Identification of cell-wall stress as a hexose-dependent and osmosensitive regulator of plant responses. Plant J. 57: 1015–1026. DOI: 10.1111/j.1365-313X.2008.03744.x.
-
Heisler MG, Hamant O, Krupinski P, Uyttewaal M, Ohno C, Jönsson H, Traas J, Meyerowitz EM. 2010. Alignment between PIN1 polarity and microtubule orientation in the shoot apical meristem reveals a tight coupling between morphogenesis and auxin transport. PLoS Biol. 8: e1000516. DOI: 10.1371/journal.pbio.1000516.
-
Hellgren JM, Olofsson K, Sundberg B. 2004. Patterns of auxin distribution during gravitational induction of reaction wood in poplar and pine. Plant Physiol. 135: 212–220. DOI: 10.1104/pp.104.038927.
-
Karczewska D, Karczewski J, Włoch W, Jura-Morawiec J, Kojs P, Iqbal M, Krawczyszyn J. 2009. Mathematical modeling of intrusive growth of fusiform initials in relation to radial growth and expanding cambial circumference in Pinus sylvestris L. Acta Biotheor. 57: 331–348. DOI: 10.1007/s10441-009-9068-y.
-
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: 315–331. DOI: 10.1163/22941932-20160136.
-
Klepper B, Browning VD, Taylor HM. 1971. Stem diameter in relation to plant water status. Plant Physiol. 48: 683–685. DOI: 10.1104/pp.48.6.683.
-
Klisz M, Wojda T, Jastrzębowski S, Ukalska J. 2015. Circumferential variation in heartwood in stands of black locust (Robinia pseudoacacia L.). Drewno 58: 31–44. DOI: 10.12841/wood.1644-3985.116.03.
-
Kojs P, Rusin T. 2011. Diurnal strains in plants. In: Gliński J, Horabik J, Lipiec J (eds.), Encyclopedia of agrophysics: 220–224. Springer, Dordrecht. DOI: 10.1007/978-90-481-3585-1_203.
-
Kozlowski TT, Winget CH. 1964. Diurnal and seasonal variation in radii of tree stems. Ecology 45: 149–155. DOI: 10.2307/1937115.
-
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: 1021–1027. DOI: 10.1093/aob/mcu026.
-
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: 455–464. DOI: 10.1007/s10086-015-1487-6.
-
Kurusu T, Nishikawa D, Yamazaki Y, Gotoh M, Nakano M, Hamada H, Yamanaka T, Iida K, Nakagawa Y, Saji H, Shinozaki K, Iida H, Kuchitsu K. 2012a. Plasma membrane protein OsMCA1 is involved in regulation of hypo-osmotic shock-induced Ca2+ influx and modulates generation of reactive oxygen species in cultured rice cells. BMC Plant Biol. 12: 11. DOI: 10.1186/1471-2229-12-11.
-
Kurusu T, Yamanaka T, Nakano M, Takiguchi A, Ogasawara Y, Hayashi T, Iida K, Hanamata S, Shinozaki K, Iida H, Kuchitsu K. 2012b. Involvement of the putative Ca2+-permeable mechanosensitive channels, NtMCA1 and NtMCA2, in Ca2+ uptake, Ca2+-dependent cell proliferation and mechanical stress-induced gene expression in tobacco (Nicotiana tabacum) BY-2 cells. J. Plant Res. 125: 555–568. DOI: 10.1007/s10265-011-0462-6.
-
Lilley JLS, Gee CW, Sairanen I, Ljung K, Nemhauser JL. 2012. An endogenous carbon-sensing pathway triggers increased auxin flux and hypocotyl elongation. Plant Physiol. 160: 2261–2270. DOI: 10.1104/pp.112.205575.
-
Littell RC, Milliken GA, Stroup WW, Wolfinger RD, Schabenberger O. 2006. SAS for mixed models, 2nd Edn. SAS Institute Inc., Cary, NC.
-
Los DA, Murata N. 2004. Membrane fluidity and its roles in the perception of environmental signals. Biochim. Biophys. Acta 1666: 142–157. DOI: 10.1016/j.bbamem.2004.08.002.
-
Michelot A, Simard S, Rathgeber C, Dufrêne E, Damesin C. 2012. Comparing the intra-annual wood formation of three European species (Fagus sylvatica, Quercus petraea and Pinus sylvestris) as related to leaf phenology and non-structural carbohydrate dynamics. Tree Physiol. 32: 1033–1045. DOI: 10.1093/treephys/tps052.
-
Monshausen GB, Haswell ES. 2013. A force of nature: molecular mechanisms of mechanoperception in plants. J. Exp. Bot. 64: 4663–4680. DOI: 10.1093/jxb/ert204.
-
Nakayama N, Smith RS, Mandel T, Robinson S, Kimura S, Boudaoud A, Kuhlemeier C. 2012. Mechanical regulation of auxin-mediated growth. Curr. Biol. 22: 1468–1476. DOI: 10.1016/j.cub.2012.06.050.
-
Oribe Y, Funada R, Kubo T. 2003. Relationships between cambial activity, cell differentiation and the localization of starch in storage tissues around the cambium in locally heated stems of Abies sachalinensis (Schmidt) Masters. Trees 17: 185–192. DOI: 10.1007/s00468-002-0231-1.
-
Paciorek T, Zažímalová E, Ruthardt N, Petrášek J, Stierhof Y-D, Kleine-Vehn J, Morris DA, Emans N, Jürgens G, Geldner N, Friml J. 2005. Auxin inhibits endocytosis and promotes its own efflux from cells. Nature 435: 1251–1256. DOI: 10.1038/nature03633.
-
Patetta M. 2002. Longitudinal data analysis with discrete and continuous responses course notes. SAS Institute Inc., Cary, NC.
-
Panchen ZA, Primack RB, Nordt B, Ellwood ER, Stevens A-D, Renner SS, Willis CG, Fahey R, Whittemore A, Du Y, Davis CC. 2014. Leaf out times of temperate woody plants are related to phylogeny, deciduousness, growth habit and wood anatomy. New Phytol. 203: 1208–1219. DOI: 10.1111/nph.12892.
-
Puchałka R, Koprowski M, Gričar J, Przybylak R. 2017. Does tree-ring formation follow leaf phenology in Pedunculate oak (Quercus robur L.)? Eur. J. For. Res. 136: 259–268. DOI: 10.1007/s10342-017-1026-7.
-
Rahman MH, Begum S, Nakaba S, Yamagishi Y, Kudo K, Nabeshima E, Nugroho WD, Oribe Y, Funada R. 2016. Relationship between the earlywood-to-latewood transition and changes in levels of stored starch around the cambium in locally heated stems of the evergreen conifer Chamaecyparis pisifera. Trees 30: 1619–1631. DOI: 10.1007/s00468-016-1395-4.
-
Rahman MH, Kudo K, Begum S, Yamagishi Y, Muraishi T, Nakaba S, Oribe Y, Lee C, Jin H-O, Funada R. 2018. Effects of auxin-transport-inhibitor and defoliation on wood formation in locally-heated Abies homolepis. IAWA J. 39: 353–371. DOI: 10.1163/22941932-20170211.
-
Rayle DL, Cleland RE. 1992. The acid growth theory of auxin-induced cell elongation is alive and well. Plant Physiol. 99: 1271–1274. DOI: 10.1104/pp.99.4.1271.
-
Rédei K, Osváth-Bujtás Z, Balla I. 2002. Clonal approaches to growing black locust (Robinia pseudoacacia) in Hungary: a review. Forestry 75: 547–552. DOI: 10.1093/forestry/75.5.547.
-
Sairanen I, Novák O, Pěnčík A, Ikeda Y, Jones B, Sandberg G, Ljung K. 2012. Soluble carbohydrates regulate auxin biosynthesis via PIF proteins in Arabidopsis. Plant Cell 24: 4907–4916. DOI: 10.1105/tpc.112.104794.
-
SAS Institute. 2017. SAS/STAT 14.3 user’s guide. SAS Institute Inc., Cary, NC, USA.
-
Sass-Klaassen U, Sabajo CR, den Ouden J. 2011. Vessel formation in relation to leaf phenology in pedunculate oak and European ash. Dendrochronologia 29: 171–175. DOI: 10.1016/j.dendro.2011.01.002.
-
Savidge RA, Wareing PF. 1981. Plant-growth regulators and the differentiation of vascular elements. In: Barnett JR (ed.), Xylem cell development: 192–235. Castle House Publications, Tunbridge Wells.
-
Schrader J, Baba K, May ST, Palme K, Bennett M, Bhalerao RP, Sandberg G. 2003. Polar auxin transport in the wood-forming tissues of hybrid aspen is under simultaneous control of developmental and environmental signals. Proc. Natl. Acad. Sci. U.S.A. 100: 10096–10101. DOI: 10.1073/pnas.1633693100.
-
Simonneau T, Habib R, Goutouly J-P, Huguet J-G. 1993. Diurnal changes in stem diameter depend upon variations in water content: direct evidence in peach trees. J. Exp. Bot. 44: 615–621. DOI: 10.1093/jxb/44.3.615.
-
Srivastava LM. 1973. Cambial activity in trees. Arnoldia 33: 46–66.
-
Sun J, Qi L, Li Y, Chu J, Li C. 2012. PIF4-mediated activation of YUCCA8 expression integrates temperature into the auxin pathway in regulating Arabidopsis hypocotyl growth. PLoS Genet. 8: e1002594. DOI: 10.1371/journal.pgen.1002594.
-
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: 615–624. DOI: 10.1007/s11284-013-1053-x.
-
Ueda M, Shibata E. 2001. Diurnal changes in branch diameter as indicator of water status of Hinoki cypress Chamaecyparis obtusa. Trees 15: 315–318. DOI: 10.1007/s004680100113.
-
Uggla C, Mellerowicz EJ, Sundberg B. 1998. Indole-3-acetic acid controls cambial growth in Scots pine by positional signaling. Plant Physiol. 117: 113–121. DOI: 10.1104/pp.117.1.113.
-
Vavrčík H, Gryc V, Rybníček M. 2008. Fluorescence microscopy utilization for lignin detection in wooden cell walls in spruce. A technical note. In: Elferts D, Brumelis G, Gärtner H, Helle G, Schleser G (eds.), Proceedings of the dendrosymposium 2007. Scientific Technical Report (STR): Vol. 08/05. 6. TRACE (Tree Rings in Archaeology, Climatology and Ecology) conference: 176–182. DOI: 10.2312/GFZ.b103-08056.
-
Veley KM, Marshburn S, Clure CE, Haswell ES. 2012. Mechanosensitive channels protect plastids from hypoosmotic stress during normal plant growth. Curr. Biol. 22: 408–413. DOI: 10.1016/j.cub.2012.01.027.
-
Wodzicki TJ. 1993. Auxin apical control of the auxin polar transport and its oscillation — a suggested cellular transduction mechanism. Acta Soc. Bot. Pol. 62: 37–41. DOI: 10.5586/asbp.1993.007.
-
Wojda T, Klisz M, Jastrzębowski S, Mionskowski M, Szyp-Borowska I, Szczygieł K. 2015. The geographical distribution of the black locust (Robinia pseudoacacia L.) in Poland and its role on non-forest land. Pap. Glob. Change 22: 101–113. DOI: 10.1515/igbp-2015-0018.
-
Wormit A, Butt SM, Chairam I, McKenna JF, Nunes-Nesi A, Kjaer L, O’Donnelly K, Fernie AR, Woscholski R, Barter MCL, Hamann T. 2012. Osmosensitive changes of carbohydrate metabolism in response to cellulose biosynthesis inhibition. Plant Physiol. 159: 105–117. DOI: 10.1104/pp.112.195198.
-
Yoshida M, Ikawa M, Kaneda K, Okuyama T. 2003. Stem tangential strain on the tension wood side of Fagus crenata saplings. J Wood Sci 49: 475–478. DOI: 10.1007/s10086-002-0511-9.
-
Zakrzewski J. 1983. Hormonal control of cambial activity and vessel differentiation in Quercus robur. Physiol. Plant. 57: 537–542. DOI: 10.1111/j.1399-3054.1983.tb02782.x.
-
Zhang W, Fan L-M, Wu W-H. 2007. Osmo-sensitive and stretch-activated calcium-permeable channels in Vicia faba guard cells are regulated by actin dynamics. Plant Physiol. 143: 1140–1151. DOI: 10.1104/pp.106.091405.
-
Zweifel R, Item H, Häsler R. 2000. Stem radius changes and their relation to stored water in stems of young Norway spruce trees. Trees 15: 50–57. DOI: 10.1007/s004680000072.
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Direct exposure to solar radiation causes radial growth eccentricity at the beginning of the growing season in Robinia pseudoacacia
In: IAWA JournalSearch for other papers by Adam Miodek in
Current site
Google Scholar
PubMed
Search for other papers by Aldona Gizińska in
Current site
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PubMed
Search for other papers by Marcin Klisz in
Current site
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Search for other papers by Tomasz Wojda in
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PubMed
Search for other papers by Krzysztof Ukalski in
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PubMed
Abstract
Our study investigated the effect of stem temperature increase on xylem formation in Robinia pseudoacacia tree-trunks, caused by direct exposure to solar radiation. It is important to determine factors which may improve the concentricity of deposited wood tissue and intensify xylogenesis because a strong irregularity of wood tissue deposited in the radial direction in mature trees of R. pseudoacacia reduces the commercial value of the wood. Samples of vascular cambium along with adjacent tissues were collected from the southern (illuminated) and northern (shaded) side of tree-trunks growing in the inner and peripheral (thus exposed to direct sunlight) zones of the research plot. Sampling was performed several times during the growing season. The collected material was examined by epifluorescence microscopy and the thickness of deposited tissue comprising cambial xylem derivatives was measured. Deposition of a markedly greater amount of xylem on the southern side of tree-trunks in the peripheral zone of the plot was observed before full leaf development. Instrumental climatic data confirmed that in the early stage of the growing season, temperature on the southern side of the peripheral zone tree-trunk was higher than on the northern side. No clear response in terms of directional deposition of xylem was noticed in the inner zone trees and in peripheral zone trees after full leaf development. This study highlights the importance of temperature increase, caused by solar radiation, for R. pseudoacacia xylogenesis, which may be considered as a factor that affects the course of the radial growth before full leaf development.
| All Time | Past Year | Past 30 Days | |
|---|---|---|---|
| Abstract Views | 670 | 104 | 5 |
| Full Text Views | 56 | 5 | 0 |
| PDF Views & Downloads | 58 | 6 | 0 |