Plant size and abiotic factors determine the intra-specific variation in the multi-stemmed architecture of Prunus lusitanica in the Northeast limit of its global distribution

  • A. Muñoz Costa Centro de investigación La Orden-Valdesequera. Guadajira, Badajoz.
  • J.A. Calleja-Alarcón Dpto. Biología Animal, Vegetal y Ecología. Universidad Autónoma de Barcelona. Barcelona.

Abstract

Aim of study: The present work provides novel insights on factors (either intrinsic or extrinsic) that trigger sprouting in woody species living at range margins. We aim to explain the inter-individual variability in the multi-stemmed architecture of Prunus lusitanica L., an Iberian evergreen relict tree related to the Tertiary flora.

Area of study: Northeastern Mediterranean mountains of the Iberian Peninsula, the Northeast limit of the global distribution of the species.

Material and Methods: We gathered data on two modes of vegetative reproduction, basal and layering sprouts, in 288 clumps of Prunus lusitanica from four populations. We modeled and analyzed the effect of environmental factors (topography, canopy cover, soil moisture and disturbances) and plant size (diameter at breast height) on sprouting by means of Generalized Linear Model and other statistical approaches.

Main results: Plant size arises as the principal factor to explain the variability of the numbers of both types of sprouts yet it is not a trigger factor. Natural and anthropogenic disturbances promote basal and layering shoots, while tree canopy is mainly relevant for basal shoots, and slope and soil moisture are significant factors for layering shoots.

Research highlights: The multi-stemmed architecture of P. lusitanica at the Northeastern limit of its worldwide distribution is triggered by local environmental factors and disturbances. Each external factor shows different levels of influence on the variability and type of vegetative reproduction yet the intensity of the response is driven by the size of the largest trunk of each clump.

Key words: vegetative reproduction; sprouting; disturbances; woody plants; relict tree; subtropical; Iberian Peninsula.

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Author Biography

A. Muñoz Costa, Centro de investigación La Orden-Valdesequera. Guadajira, Badajoz.
Departamento de producción forestal

References

Aymerich P, Sáez Ll, Blanché C, 2010. Llibre vermell de les plantes vasculars endèmiques i amenaçades de Catalunya. Argania Editio. Barcelona, Spain. 255 pp.

Barrón E, Peyrot D, 2006. La vegetación forestal en el Terciario. In: Paleoambientes y cambio climático (Carrión JS, Fernández S, Fuentes N, eds). Fundación Séneca – Agencia de Ciencia y Tecnología de la Región de Murcia. pp: 54-76.

Bazzaz F, Chiariello N, Coley P, Pitelka P, 1987. Allocation Resources to Reproduction and Defense. BioScience 37: 58-67. http://dx.doi.org/10.2307/1310178

Bellingham PJ, Sparrow AD, 2009. Multi-stemmed trees in montane rain forests: their frequency and demography in relation to elevation, soil nutrients and disturbance. J Ecol 97: 472-483. http://dx.doi.org/10.1111/j.1365-2745.2009.01479.x

Bellingham PJ, Tanner EVJ, Healey JR, 1994. Sprouting of trees in Jamaican montane forests, after a hurricane. J Ecol 82: 747-758. http://dx.doi.org/10.2307/2261440

Bond WJ, Midgley JJ, 2001. Ecology of sprouting in woody plants: the persistence niche. Trends Ecol Evol 16: 45-51. http://dx.doi.org/10.1016/S0169-5347(00)02033-4

Bond WJ, Midgley JJ, 2003. The evolutionary ecology of sprouting in woody plants. Int J Plant Sci 164: S103-S114. http://dx.doi.org/10.1086/374191

Bond WJ, Van Wilgen BW, 1996. Fire and plants. Chapman & Hall, London. 272 pp. http://dx.doi.org/10.1007/978-94-009-1499-5

Boninsegna JA, Villalba R, Amarilla L, Ocampo J, 1989. Studies on tree rings, growth rates and age-size relationships of tropical tree species in Misiones, Argentina. IAWA Bull 10: 161-169.

Calleja JA, 2006. Geobotánica, estructura demográf ica, conservación y biología predispersiva de Prunus lusitanica (loro) en la Península ibérica. Memoria de tesis doctoral. Universidad Autónoma de Madrid, Facultad de Ciencias, Departamento de Biología.

Calleja JA, 2011. Tama-os poblacionales, estructura poblacional y regeneración de Prunus lusitanica en el NE de la Península Ibérica. Orsis 26: 21-35.

Calleja JA, Benito M, Sainz H, 2009. A quaternary perspective on the conservation prospects of the Tertiary relict tree Prunus lusitanica. J Biogeog 36: 487-498. http://dx.doi.org/10.1111/j.1365-2699.2008.01976.x

Calleja JA, Sainz H, 2009. Análisis e interpretación geobotánica de la estructura y composición florística de las loreras ibéricas. Ecología 22: 45-71.

Calleja JA, Domínguez F, Sainz H, 2008. Prunus lusitanica L. In: Atlas y Libro Rojo de la Flora Vascular Amenazada de Espa-a. Adenda 2008 (Ba-ares Á, Blanca G, Güemes J, Moreno JC, Ortiz S, eds). Dirección General de Conservación de la Naturaleza. Madrid, Spain. pp: 110-111.

Chin SW, Wen J, Johnson G, Potter D, 2010. Merging Maddenia with the morphologically diverse Prunus (Rosaceae). Bot J Linn Soc 164: 236-245. http://dx.doi.org/10.1111/j.1095-8339.2010.01083.x

Clarke PJ, Lawes MJ, Midgley JJ, 2010. Resprouting as a key functional trait in woody plants – challenges to developing new organizing principles. New Phytol 188: 651-654. http://dx.doi.org/10.1111/j.1469-8137.2010.03508.x PMid:20976869

Cornelissen JHC, Lavorel S, Garnier E, Díaz S, Buchmann N, Gurvich DE et al., 2003. A handbook of protocols for standardised and easy measurement of plant functional traits worldwide. Aust J Bot 51: 335-380. http://dx.doi.org/10.1071/BT02124

Del Tredici P, 2001. Sprouting in temperate trees: a morphological and ecological review. Bot Rev 67: 121-140. http://dx.doi.org/10.1007/BF02858075

Fernández-Palacios JM, Arévalo JR, 1998. Regeneration strategies of tree species in the laurel forest of Tenerife (The Canary Islands). Plant Ecol 137: 21-29. http://dx.doi.org/10.1023/A:1008000330184

Franco JA, 1964. O azereiro e as ginjeiras bravas. Bol Soc Port Ci Nat 10: 66-90.

Fujiki D, Kikuzawa K, 2006. Stem turnover strategy of multiple-stemmed woody plants. Ecol Res 2: 80-386.

García M, Maldonado J, Morla C, Sainz H, 2002. Fitogeografía histórica de la península Ibérica. In: La diversidad biológica de España (Pineda FD, De Miguel JM, Casado MA, Montalvo J, eds). Prentice Hall, Madrid, Spain. pp: 45-64.

García D, Zamora R, 2003. Persistence, multiple demographic strategies and conservation in long-lived Mediterranean plants. J Veg Scie 14: 921-926. http://dx.doi.org/10.1111/j.1654-1103.2003.tb02227.x

Garilleti R, Calleja JA, Lara F, 2012. La vegetación ribere-a de los ríos y ramblas de la España meridional (península y archipiélagos). Ministerio de Agricultura, Alimentación y Medio Ambiente, Madrid, Spain.

Hara M, 1987. Analysis of Seedling banks of a climax beech forest: ecological importance of seedling sprouts. Vegetatio 71: 67-74.

Harper JL, 1977. Population biology of plants. Academic Press, London. 892 pp.

Jonsdottir IS, Watson MA, 1997. Extensive physiological integration: an adaptative trait in resource-poor environ-ments? In: The ecology and evolution of clonal plants (Kroon H, Groendael J, eds). Backhuys Publishers, Leiden. pp: 109-136.

Kammesheidt L, 1999. Forest recovery by root suckers and above-ground sprouts after slash-and-burn agriculture, fire and logging in Paraguay and Venezuela. J Trop Ecol 15: 143-157. http://dx.doi.org/10.1017/S0266467499000723

Kawecki TJ, 20,08. Adaptation to marginal habitats. Annu Rev Ecol Evol Syst 39: 321-342. http://dx.doi.org/10.1146/annurev.ecolsys.38.091206.095622

Klimês J, Klimês L, 2007. Bud banks and their role in vegetative regeneration – A literature review and proposal for simple classification and assessment. Perspect Plant Ecol 8: 115-129. http://dx.doi.org/10.1016/j.ppees.2006.10.002

Klimês L, Klimêsova J, Hendriks R, Van Groenendael J, 1997. Clonal plant architecture: a comparative analysis of form and function. In: The ecology and evolution of clonal plants (Kroon H, Groenendael J, eds). Backhuys Publishers, Leiden. pp: 1-29.

Kobe R, 1999. Light gradient partitioning among tropical tree species through differential seedling mortality and growth. Ecology 80: 187-201. http://dx.doi.org/10.1890/0012-9658(1999)080[0187:LGPATT]2.0.CO;2

Konstantinidis P, Tsiourlis G, Xofis P, 2006. Effect of fire season, aspect and pre-fire plant size on the growth of Arbutus unedo L. (strawberry tree) resprouts. Forest Ecol Manag 225: 359-367. http://dx.doi.org/10.1016/j.foreco.2006.01.011

Koop H, 1987. Vegetative reproduction of trees in some European natural forests. Vegetatio 72: 103-110.

Lara F, Garilleti R, Calleja JA, 2004. La vegetación de ribera de la mitad norte espa-ola. CEDEX, Madrid, Spain. 530 pp.

Lieberman D, Lieberman M, Hartshorn G, Peralta R, 1985. Growth rates and age-size relationships of tropical wet forest trees in Costa Rica. J Trop Ecol 1: 97-109. http://dx.doi.org/10.1017/S026646740000016X

Matula R, Svátek M, Ku° rová J, Úradníc˘ek L, Kadavy´ J, Kneifl M, 2012. The sprouting ability of the main tree species in Central European coppices: implications for coppice restoration. Eur J Forest Res 131: 1501-1511. http://dx.doi.org/10.1007/s10342-012-0618-5

Nagaike T, Kubota Y, Watanabe M, 1999. The effects of selective logging on stand structure and the regeneration of subboreal forest in Hokkaido, Northern Japan. J For Res 4: 41-45. http://dx.doi.org/10.1007/BF02760323

Nakamura F, Inahara S, 2007. Fluvial geomorphic disturbances and life history traits of riparian tree species. In: Plant Disturbance Ecology (Johnson EA, Miyanishi K, eds). Elsevier Academic Press, San Diego, California, USA. pp: 283-310. http://dx.doi.org/10.1016/B978-012088778-1/50011-X PMid:17880910

Paula S, Ojeda F, 2006. Resistance of three co-occurring resprouter Erica species to highly frequent disturbance. Plant Ecol 183: 329-336. http://dx.doi.org/10.1007/s11258-005-9043-x

Peterson CJ, Jones RH, 1997. Clonality in woody plants: a review and comparison with clonal herbs. In: The ecology and evolution of clonal plants (Kroon H, Groendael J, eds). Backhuys Publishers, Leiden. pp: 263-289.

Pignatti S, 1978. Evolutionary trends in Mediterranean flora and vegetation. Vegetatio 37: 175-185. http://dx.doi.org/10.1007/BF00717651

Sands BA, Abrams MD, 2009. Effects of stump diameter on sprout number and size for three oak Species in a Pennsylvania clearcut. North J Appl For 26:122-125.

Santiago R, 2001. Prunus lusitanica en la Península Ibérica. Memoria de tesis doctoral. Universidad Politécnica de Madrid (Spain), Escuela de Técnicos Superiores de Ingenieros de Montes, Departamento de Silvopascicultura.

SPSS Inc, 2006. Statistical Package for the Social Sciences. SPSS developersworks.

Tanentzap AJ, Mountford EP, Cooke AS, Coomes DA, 2012. The more stems the merrier: advantages of multistemmed architecture for the demography of understory trees in a temperate broadleaf woodland. J Ecol 100: 171-183. http://dx.doi.org/10.1111/j.1365-2745.2011.01879.x

Vila M, Terradas J, 1995a. Effects of Nutrient Availability and Neighbors on Shoot Growth, Resprouting and Flowering of Erica multiflora. J Veg Sci 6: 411-416. http://dx.doi.org/10.2307/3236240

Vila M, Terradas J, 1995b. Effects of competition and disturbance on the resprouting performance of the mediterranean shrub erica multiflora l (ericaceae). AM J Bot 82: 1241-1248. http://dx.doi.org/10.2307/2446246

Watson MA, Hay MJM, Newton PCD, 1997. Developmental phenology and the timing of determination of shoot bud fates: ways in which the developmental program modulates fitness in clonal plants. In: The ecology and evolution of clonal plants (Kroon H, Groendael J, eds). Backhuys Publishers, Leiden. pp: 31-53.

William E, 1986. A guide for estimating cover. Rangelands 8: 236-238.

Published
2013-12-01
How to Cite
Muñoz Costa, A., & Calleja-Alarcón, J. (2013). Plant size and abiotic factors determine the intra-specific variation in the multi-stemmed architecture of Prunus lusitanica in the Northeast limit of its global distribution. Forest Systems, 22(3), 423-432. https://doi.org/10.5424/fs/2013223-03546
Section
Research Articles