Tree Genetics & Genomes

, Volume 10, Issue 5, pp 1191–1203 | Cite as

Among-population variation and plasticity to drought of Atlantic, Mediterranean, and interprovenance hybrid populations of maritime pine

Original Paper

Abstract

Maritime pine grows naturally under a wide range of climatic conditions, from strongly Atlantic to strongly Mediterranean. Aiming to improve our understanding of the genetic structure and inheritance of drought resistance strategies in the species, we conducted an environmentally controlled experiment to assess the genetic variation and plasticity to drought of Atlantic and Mediterranean populations, and the interprovenance hybrids between them. Hybridization could also help to provide new genetic material for use in transitional areas between the two regions, for which reproductive materials of good quality are generally lacking. Plastic responses to water stress appeared to be highly conserved among populations, with a common conservative isohydric strategy based on promoting growth when water was abundant, and stopping it when water became limiting. We found, however, a strong intraspecific variation in biomass allocation patterns. The Atlantic populations showed a risky growth-based strategy with a larger amount of juvenile needles, whereas Mediterranean populations showed a more conservative strategy, minimizing aerial growth and increasing the proportion of adult needles that is more resistant to water loss. Hybrid populations performed more similarly to the Mediterranean parent, suggesting a dominance of the Mediterranean-like characteristics. Some of the tested hybrid populations, however, combined high growth with traits of drought adaptation, and thus represent potentially interesting materials for use in transitional regions between the two climate zones.

Keywords

Phenotypic plasticity Drought stress Pinus pinaster Interprovenance hybrids Biomass allocation Optimal partitioning theory 

Supplementary material

11295_2014_753_MOESM1_ESM.pdf (139 kb)
Online Resource 1(PDF 138 kb)
11295_2014_753_MOESM2_ESM.pdf (1.9 mb)
Online Resource 2(PDF 1952 kb)
11295_2014_753_MOESM3_ESM.pdf (109 kb)
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References

  1. Alberto FJ, Aitken SN, Alía R, González-Martínez SC, Häninen H et al (2013) Potential for evolutionary responses to climate change—evidence from tree populations. Glob Chang Biol 19:1645–1661PubMedCrossRefPubMedCentralGoogle Scholar
  2. Aranda I, Alía R, Ortega U, Dantas AK, Majada J (2010) Intra-specific variability in biomass partitioning and carbon isotopic discrimination under moderate drought stress in seedlings from four Pinus pinaster populations. Tree Genet Genomes 6:169–178CrossRefGoogle Scholar
  3. Bloom AJ, Chapin FS, Mooney HA (1985) Resource limitation in plants—an economic analogy. Annu Rev Ecol Syst 16:363–392Google Scholar
  4. Bolstad SB, Kang H, Guries RP, Marty TL (1991) Performance of interprovenance and intraprovenance crosses of jack pine in Central Wisconsin. Silvae Genet 40:124–130Google Scholar
  5. Cendán C, Sampedro L, Zas R (2013) The maternal environment determines the timing of germination in Pinus pinaster. Env Exp Bot 94:66–72CrossRefGoogle Scholar
  6. Chambel MR, Climent J, Alía R (2007) Divergence among species and populations of Mediterranean pines in biomass allocation of seedlings grown under two watering regimes. Ann For Sci 64:87–97CrossRefGoogle Scholar
  7. Climent J, Silva FCE, Chambel MR, Pardos M, Almeida MH (2009) Freezing injury in primary and secondary needles of Mediterranean pine species of contrasting ecological niches. Ann For Sci 66:407CrossRefGoogle Scholar
  8. Cody ML (1986) Roots in plant ecology. Trends Ecol Evol 1:76–78PubMedCrossRefGoogle Scholar
  9. Coleman JS, McConnaughay KDM, Ackerly DD (1994) Interpreting phenotypic variation in plants. Trends Ecol Evol 9:187–191PubMedCrossRefGoogle Scholar
  10. Corcuera L, Gil-Pelegrín E, Notivol E (2010) Phenotypic plasticity in Pinus pinaster delta(13)C: environment modulates genetic variation. Ann For Sci 67:812CrossRefGoogle Scholar
  11. Corcuera L, Cochard H, Gil-Pelegrín E, Notivol E (2011) Phenotypic plasticity in mesic populations of Pinus pinaster improves resistance ti xylem embolism (P50) under severe drought. Trees 25:1033–1042CrossRefGoogle Scholar
  12. Corcuera L, Gil-Pelegrín E, Notivol E (2012) Differences in hydraulic architecture between mesic and xeric Pinus pinaster populations at the seedling stage. Tree Physiol 32:1442–1457PubMedCrossRefGoogle Scholar
  13. Correia I, Almeida MH, Aguiar A, Alía R, David TS, Pereira JS (2008) Variations in growth, survival and carbon isotope composition (13C) among Pinus pinaster populations of different geographic origins. Tree Physiol 28:1545–1552PubMedCrossRefGoogle Scholar
  14. Danjon F, González G, Meredieu C et al (2009) Phenotypic plasticity of Pinus pinaster to water stress: biomass allocation and root architecture. In: International Symposium “Root Research and Applications”, RootRAP, Boku, Vienna, Austria, 2–4 SeptemberGoogle Scholar
  15. Darrow HE, Bannister P, Burritt DJ, Jameson PE (2002) Are juvenile forms of New Zealand heteroblastic trees more resistant to water loss than their mature counterparts? N Z J Bot 40:313–325CrossRefGoogle Scholar
  16. de la Mata R, Zas R (2010a) Performance of maritime pine Spanish Mediterranean provenances at young ages in a transitional region between Atlantic and Mediterranean climates in NW Spain. Silvae Genet 59:8–17Google Scholar
  17. de la Mata R, Zas R (2010b) Transferring Atlantic maritime pine improved material to a region with marked Mediterranean influence in inland NW Spain: a likelihood-base approach on spatially adjusted field data. Eur J For Res 129:645–658CrossRefGoogle Scholar
  18. Eriksson G, Ilstedt B (1986) Stem volume of intra- and interprovenance families of Picea abies (L.) Karst. Scand J For Res 1:141–152CrossRefGoogle Scholar
  19. Fernández M, Gil L, Pardos JA (1999) Response of Pinus pinaster Ait. provenances at early age to water supply. I. Water relation parameters. Ann For Sci 56:179–187CrossRefGoogle Scholar
  20. Fernández M, Gil L, Pardos JA (2000) Effects of water supply on gas exchange in Pinus pinaster Ait. provenances during their first growing season. Ann For Sci 57:9–16CrossRefGoogle Scholar
  21. Gaspar MJ, Velasco T, Feito I, Alía R, Majada J (2013) Genetic variation of drought tolerance in Pinus pinaster at three hierarchical levels: a comparison of induced osmotic stress and field testing. PLoS ONE 8(11):e79094PubMedCrossRefPubMedCentralGoogle Scholar
  22. González-Martínez SC, Mariette S, Ribeiro MM, Burban C et al (2004) Genetic resources in maritime pine (Pinus pinaster Aiton): molecular and quantitative measures of genetic variation and differentiation among maternal lineages. For Ecol Manag 197:103–115CrossRefGoogle Scholar
  23. Grotkopp E, Rejmánek M, Rost TL (2002) Toward a causal explanation of plant invasiveness: seedling growth and life-history strategies of 29 pine (Pinus) species. Am Nat 159(4):396–419PubMedCrossRefGoogle Scholar
  24. Harfouche A, Kremer A (2000) Provenance hybridization in a diallel mating scheme of maritime pine (Pinus pinaster). I. Means and variance components. Can J For Res 30:1–9CrossRefGoogle Scholar
  25. Harfouche A, Baradat P, Kremer A (1995) Variabilité intraspécifique chez le pin maritime (Pinus pinaster Ait) dans le sud-est de la France. II. Hétérosis et combinaison de caractères chez des hybrides interraciaux. Ann For Sci 52:329–346CrossRefGoogle Scholar
  26. IPCC (2007) Intergovernmental Panel on Climate Change, Fourth Assessment Report. In: Pachauri R, Reisinger A (eds). Geneva, Switzerland, p 104Google Scholar
  27. Kaya Z, Lindgren D (1992) The genetic variation of inter-provenance hybrids of Picea abies and possible breeding consequences. Scand J For Res 7:15–26CrossRefGoogle Scholar
  28. Lamy JB, Delzon S, Bouche P, Alía R, Vendramin GG et al (2014) Limited genetic variability and phenotypic plasticity detected for cavitation resistance in a Mediterranean pine. New Phytol 201:874–886PubMedCrossRefGoogle Scholar
  29. Larcher W (1995) Physiological plant ecology. Ecophysiology and stress physiology of functional groups. Springer, Berlin-HeidelbergGoogle Scholar
  30. Leck MA, Parker VT, Simpson RL (2008) Seedling ecology and evolution. Cambridge University Press, CambridgeCrossRefGoogle Scholar
  31. Littell RC, Milliken GA, Stroup WW, Wolfinger RD, Schabenberger O (2006) SAS System for mixed models, 2nd edn. SAS Institute, CaryGoogle Scholar
  32. Ludlow MM (1989) Strategies of response to water stress. In: Kreeb KH, Richter H, Hinckley TM (eds) Structural and functional responses to environmental stresses: water shortage. SPB Academic Publishing, The Hague, pp 269–281Google Scholar
  33. Martínez-Ferri E, Balaguer L, Valladares F, Chico JM, Manrique E (2000) Energy dissipation in drought-avoiding and drought-tolerant tree species at midday during the Mediterranean summer. Tree Physiol 20:131–138PubMedCrossRefGoogle Scholar
  34. Müller I, Schmid B, Weiner J (2000) The effect of nutrient availability on biomass allocation patterns in 27 species of herbaceous plants. Perspect Plant Ecol 3:115–127CrossRefGoogle Scholar
  35. Nguyen A, Lamant A (1989) Variation in growth and osmotic regulation of roots of water-stressed maritime pine (Pinus pinaster Ait.) provenances. Tree Physiol 5:123–133PubMedCrossRefGoogle Scholar
  36. Nguyen-Queyrens A, Costa P, Loustau D, Plomion C (2002) Osmotic adjustment in Pinus pinaster cuttings in response to a soil drying cycle. Ann For Sci 59:795–799CrossRefGoogle Scholar
  37. Niklas KJ (1994) Allometry in plants: the scaling of form and process. University of Chicago Press, ChicagoGoogle Scholar
  38. O’Brien EK, Mazanec RA, Krauss SL (2007) Provenance variation of ecologically important traits of forest trees: implications for restoration. J Appl Ecol 44:583–593CrossRefGoogle Scholar
  39. Osório J, Osório ML, Chaves MM, Pereira JS (1998) Water deficits are more important in delaying growth than in changing patterns of carbon allocation in Eucalyptus globulus. Tree Physiol 18:363–373PubMedCrossRefGoogle Scholar
  40. Pardos M, Calama R, Climent J (2009) Difference in cuticular transpiration and sclerophylly in juvenile and adult pine needles relates to the species-specific rates of development. Trees Struct Funct 23:501–508CrossRefGoogle Scholar
  41. Peters J, Morales D, Jiménez MS (2003) Gas exchange characteristics of Pinus canariensis needles in a forest stand on Tenerife, Canary Islands. Trees Struct Funct 17:492–500CrossRefGoogle Scholar
  42. Pigliucci M, Schlichting CD (1996) Reaction norms of Arabidopsis. IV. Relationships between plasticity and fitness. Heredity 76:427–436PubMedCrossRefGoogle Scholar
  43. Pigott CD, Pigott S (1993) Water as a determinant of the distribution of trees at the boundary of the Mediterranean Zone. J Ecol 81:557–566CrossRefGoogle Scholar
  44. Poorter H, Nagel O (2000) The role of biomass allocation in the growth response of plants to different levels of light, CO2, nutrients and water: a quantitative review. Aust J Plant Physiol 27:595–607CrossRefGoogle Scholar
  45. Poorter H, Niklas KJ, Reich PB, Oleksyn J, Poot P, Mommer L (2012) Biomass allocation to leaves, stems and roots: meta-analyses of interspecific variation and environmental control. New Phytol 193:30–50PubMedCrossRefGoogle Scholar
  46. Sánchez-Gómez D, Majada J, Alía R, Feito I, Aranda I (2010) Intraspecific variation in growth and allocation patterns in seedlings of Pinus pinaster Ait. submitted to contrasting watering regimes: can water availability explain regional variation? Ann For Sci 67:1–8CrossRefGoogle Scholar
  47. Shukla RP, Ramakrishnan PS (1986) Architecture and growth strategies of tropical trees in relation to successional status. J Ecol 74:33–46CrossRefGoogle Scholar
  48. Strauss SH, Ledig FT (1985) Seedling architecture and life history evolution in pines. Am Nat 125:702–715CrossRefGoogle Scholar
  49. Tognetti R, Michelozzi M, Lauteri M, Brugnoli E, Giannini R (2000) Geographic variation in growth, carbon isotope discrimination, and monoterpene composition in Pinus pinaster Ait. provenances. Can J For Res 30:1682–1690CrossRefGoogle Scholar
  50. White TL, Adams WT, Neale DB (2007) Forest genetics. CAB International, WallingfordCrossRefGoogle Scholar

Copyright information

© Springer-Verlag Berlin Heidelberg 2014

Authors and Affiliations

  1. 1.Division of Biological SciencesThe University of MontanaMissoulaUSA
  2. 2.Madera Plus Co.San Cibrao das ViñasSpain
  3. 3.Misión Biológica de Galicia, MBG-CSICPontevedraSpain

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