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Revisiting the fate of buds: size and position drive bud mortality and bursting in two coexisting Mediterranean Quercus species with contrasting leaf habit

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Abstract

Understanding the relationships between bud size and position and bud fate through time is crucial for identifying and subsequently modeling the mechanisms underlying tree architecture. However, there is a lack of information on how bud size drives crown architectural patterns in coexisting tree species. We studied bud demography in two coexisting Mediterranean oak species with contrasting leaf habit (Quercus ilex, evergreen; Q. faginea, deciduous). The main objective was to analyse the effect of bud size on the fate of buds with different positions along the shoot (apical, leaf axillary and scale-cataphyll axillary buds). The number, length and position of all buds and stems were recorded in marked branches during 4 years. Study species presented different strategies in bud production and lifespan. The evergreen species showed greater mortality rate than the deciduous one, which produced larger buds. Bud size and position were highly related since apical buds where longer than axillary ones and bud length declined basipetally along the stem. Apical buds had also higher chances of bursting than axillary ones. Within positions, longer buds presented a higher probability of bursting than shorter ones, although no absolute size threshold was found below which bud bursting was impaired. In Q. ilex, four-year-old buds were still viable and able to burst, whereas in Q. faginea practically all buds burst in their first year or died soon after. Such different bud longevities may indicate contrasting strategies in primary growth between both species. Q. ilex is able to accumulate viable buds for several ages, whereas Q. faginea seems to rely on the production of large current-year buds with high bursting probability under favourable environmental conditions.

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References

  • Alla AQ, Camarero JJ, Montserrat-Marti G (2013) Seasonal and inter-annual variability of bud development as related to climate in two co-existing Mediterranean Quercus species. Ann Bot 111:261–270. doi:10.1093/aob/mcs247

    Article  PubMed  Google Scholar 

  • Amaral Franco J (1990) Quercus. In: Castroviejo S, Laínz M, López González G, Montserrat P, Muñoz Garmendia F, Paiva J, Villa L (eds) Flora Ibérica. CSIC, Real Jardín Botánico, pp 15–36

    Google Scholar 

  • Barthélémy D, Caraglio Y (2007) Plant architecture: a dynamic, multilevel and comprehensive approach to plant form, structure and ontogeny. Ann Bot 99:375–407. doi:10.1093/aob/mcl260

    Article  PubMed  Google Scholar 

  • Buck-Sorlin GH, Bell AD (2000) Crown architecture in Quercus petraea and Q. robur: the fate of buds and shoots in relation to age, position and environmental perturbation. Forestry 73:331–349. doi:10.1093/forestry/73.4.331

    Article  Google Scholar 

  • Cline MG (1997) Concepts and terminology of apical dominance. Am J Bot 84:1064

    Article  PubMed  CAS  Google Scholar 

  • FAO (1998) World reference base for soil resources ISRIC and ISSS, Rome

  • Fontaine F, Chaar H, Colin F, Clément C, Burrus M, Druelle JL (1999) Preformation and neoformation of growth units on 3-year-old seedlings of Quercus petraea. Can J Bot 77:1623–1631. doi:10.1139/b99-138

    Article  Google Scholar 

  • Gill AM (1971) The formation, growth and fate of buds of Fraxinus americana L. in central Massachusetts. Harvard For Pap 20:1–16

    Google Scholar 

  • Harmer R (1991) The effect of bud position on branch growth and bud abscission in Quercus petraea (Matt.) Liebl. Ann Bot 67:463–468

    Google Scholar 

  • Harmer R (1992) Relationships between shoot length, bud number and branch production in Quercus petraea (Matt.). Liebl For 65:61–72. doi:10.1093/forestry/65.1.61

    Google Scholar 

  • Ishihara MI, Kikuzawa K (2009) Annual and spatial variation in shoot demography associated with masting in Betula grossa: comparison between mature trees and saplings. Ann Bot 104:1195–1205. doi:10.1093/aob/mcp217

    Article  PubMed  Google Scholar 

  • Jones M, Harper JL (1987) The influence of neighbours on the growth of trees I: the demography of buds in Betula pendula. Proc R Soc Lond 232:1–18

    Article  Google Scholar 

  • Kozlowski TT, Torrie JH, Marshall PE (1973) Predictability of shoot length from bud size in Pinus resinosa Ait. Can J For Res 3:34–38. doi:10.1139/x73-005

    Article  Google Scholar 

  • Lehtilä K, Tuomi J, Sulkinoja M (1994) Bud demography of the mountain birch Betula pubescens ssp. tortuosa near tree line. Ecology 75:945–955. doi:10.2307/1939418

    Article  Google Scholar 

  • Little CHA (1970) Apical dominance in long shoots of white pine (Pinus strobus). Can J Bot 48:239–253. doi:10.1139/b70-036

    Article  CAS  Google Scholar 

  • Ljung K, Bhalerao RP, Sandberg G (2001) Sites and homeostatic control of auxin biosynthesis in Arabidopsis during vegetative growth. Plant J 28:465–474. doi:10.1046/j.1365-313X.2001.01173.x

    Article  PubMed  CAS  Google Scholar 

  • Macdonald AD, Mothersill DH, Caesar JC (1984) Shoot development in Betula papyrifera. III. Long-shoot organogenesis. Can J Bot 62:437–445. doi:10.1139/b84-066

    Article  Google Scholar 

  • Maillette L (1982a) Structural dynamics of silver birch. I. The fates of buds. J Appl Ecol 19:203–218. doi:10.2307/2403005

    Article  Google Scholar 

  • Maillette L (1982b) Structural dynamics of silver birch. II. A matrix model of the bud population. J Appl Ecol 19:219–238. doi:10.2307/2403006

    Article  Google Scholar 

  • Maillette L (1987) Effects of bud demography and elongation patterns on Betula cordifolia near the tree line. Ecology 68:1251–1261. doi:10.2307/1939209

    Article  Google Scholar 

  • Montserrat-Martí G, Camarero JJ, Palacio S, Pérez-Rontomé C, Milla R, Albuixech J, Maestro M (2009) Summer-drought constrains the phenology and growth of two coexisting Mediterranean oaks with contrasting leaf habit: implications for their persistence and reproduction. Trees 23:787–799. doi:10.1007/s00468-009-0320-5

    Article  Google Scholar 

  • Negi GCS (2006) Leaf and bud demography and shoot growth in evergreen and deciduous trees of central Himalaya, India. Trees 20:416–429. doi:10.1007/s00468-006-0056-4

    Article  Google Scholar 

  • Nitta I, Ohsawa M (1998) Bud structure and shoot architecture of canopy and understory evergreen broad-leaved trees at their northern limit in East Asia. Ann Bot 81:115–129. doi:10.1006/anbo.1997.0545

    Article  Google Scholar 

  • Phillips IDJ (1975) Apical dominance. Ann Rev Plant Physiol 26:341–367. doi:10.1146/annurev.pp.26.060175.002013

    Article  CAS  Google Scholar 

  • Puntieri JG, Stecconi M, Barthélémy D (2002) Preformation and neoformation in shoots of Nothofagus antarctica (G. Forster) Oerst. (Nothofagaceae) shrubs from northern Patagonia. Ann Bot 89:665–673. doi:10.1093/aob/mcf108

    Article  Google Scholar 

  • Sabatier S, Barthélémy D (2001) Bud structure in relation to shoot morphology and position on the vegetative annual shoots of Juglans regia L. (Juglandaceae). Ann Bot 87:117–123. doi:10.1006/anbo.2000.1312

    Article  Google Scholar 

  • Sanz-Pérez V, Castro-Díez P (2010) Summer water stress and shade alter bud size and budburst date in three Mediterranean Quercus species. Trees 24:89–97. doi:10.1007/s00468-009-0381-5

    Article  Google Scholar 

  • Sheil D, Burslem DFRP, Alder D (1995) The interpretation and misinterpretation of mortality rate measures. J Ecol 83:331–333. doi:10.2307/2261571

    Article  Google Scholar 

  • Shimizu-Sato S, Tanaka M, Mori H (2009) Auxin–cytokinin interactions in the control of shoot branching. Plant Mol Biol 69:429–435. doi:10.1007/s11103-008-9416-3

    Article  PubMed  CAS  Google Scholar 

  • Sokal RR, Rohlf FJ (1995) Biometry: the principles and practices of statistics in biological research. WH Freeman, New York

    Google Scholar 

  • Tanaka M, Takei K, Kojima M, Sakakibara H, Mori H (2006) Auxin controls local cytokinin biosynthesis in the nodal stem in apical dominance. Plant J 45:1028–1036. doi:10.1111/j.1365-313X.2006.02656.x

    Article  PubMed  CAS  Google Scholar 

  • Tolvanen A, Schroderus J, Henry GHR (2002) Age- and stage-based bud demography of Salix arctica under contrasting muskox grazing pressure in the High Arctic. Evol Ecol 15:443–462. doi:10.1023/A:1016049301905

    Article  Google Scholar 

  • Ward WW (1964) Bud distribution and branching in red oak. Bot Gaz 125:217–220

    Article  Google Scholar 

  • Wilson BF, Kelty MJ (1994) Characteristics of shoots from the bud bank in black oak. Bull Torrey Bot Club 121:62–68. doi:10.2307/2996884

    Article  Google Scholar 

  • Zuur AF, Ieno EN, Elphick CS (2009) Mixed effects models and extensions in ecology with R. Springer, New York

    Book  Google Scholar 

Download references

Acknowledgments

A.Q.A., J.J.C. and S.P. acknowledge the support of MAEC-AECID, ARAID and the Spanish Ministerio de Ciencia e Innovación (Juan de la Cierva subprogram), respectively. This work was supported by the Spanish Ministerio de Ciencia e Innovación and FEDER (grant numbers CGL2008-04847-C02-01, CGL2010-16880 BOS, CGL2011-26654 BOS). We thank the collaborative support of the Globimed network (http://www.globimed.net) and the Spanish “Agencia Estatal de Meterorología” for providing climatic data. The authors are grateful to Guillermo Bueno for statistical advice, Jorge Albuixech for help during field work, an anonymous Communicating Editor and two anonymous reviewers for helpful comments on an earlier version of the manuscript.

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Authors and Affiliations

  1. Fakulteti i Shkencave Pyjore, Universiteti Bujqësor i Tiranës, Kodër-Kamëz, 1029, Tirana, Albania

    Arben Q. Alla

  2. ARAID-Instituto Pirenaico de Ecología (IPE-CSIC), Avda. Montañana 1005, 50080, Zaragoza, Spain

    J. Julio Camarero

  3. Dept. d’Ecologia, Fac. Biologia, University of Barcelona, Avda Diagonal 645, 08028, Barcelona, Spain

    J. Julio Camarero

  4. Instituto Pirenaico de Ecología (IPE-CSIC), Avda. Vírgen de la Victoria s/n, 27000, Jaca (Huesca), Spain

    Sara Palacio

  5. Instituto Pirenaico de Ecología (IPE-CSIC), Avda. Montañana 1005, 50080, Zaragoza, Spain

    Gabriel Montserrat-Martí

Authors
  1. Arben Q. Alla
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  2. J. Julio Camarero
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  3. Sara Palacio
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  4. Gabriel Montserrat-Martí
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Correspondence to Arben Q. Alla.

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Communicated by U. Luettge.

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Alla, A.Q., Camarero, J.J., Palacio, S. et al. Revisiting the fate of buds: size and position drive bud mortality and bursting in two coexisting Mediterranean Quercus species with contrasting leaf habit. Trees 27, 1375–1386 (2013). https://doi.org/10.1007/s00468-013-0885-x

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