Skip to main content
Log in

Plant genetic adaptedness to climatic and edaphic environment

  • Climatic and Edaphic Adaptation
  • Published:
Euphytica Aims and scope Submit manuscript

Summary

Genetic adaptation implies the shaping of population and species gene pools in response to environmental challenges. The two components of the abiotic land environment are climate and soil, both of which determine much of the evolutionary adaptedness of plants as, besides representing a set of surrounding physical, chemical and sometimes limiting traits, they determine the availability of nutrients and energy, of which they are the immediate source. Ecogeographical distribution of species and ecotypes and different physiological mechanisms and developmental patterns are good evidence of plant adaptedness to soil and climate. However, it is not always easy to determine the underlying genetics of adaptive processes, because 1) environmental factors to which the plants are responding are not always evident and are sometimes too complex, 2) several genes may be involved in the response to a given environmental factor, and 3) the same gene/s may be involved in different adaptive responses. In particular, data on Avena species and temperature as a key environmental factor will be used to illustrate some examples of climatic and edaphic adaptedness. Temperature affects the genetic evolution and geographical distribution of all organisms, and a great deal of evidence indicates that species and populations are genetically adapted to different temperature regimes. Isozymes and other molecular markers have helped in the understanding of the genetic basis of adaptedness. There are many examples of correlation between isozyme and DNA-marker variation and environmental differences. For many population geneticists, isozyme markers are just genetic markers with little or no direct involvement in adaptation. However, metabolic processes are controlled by enzymes, influenced by the environment and used to react in response to it. Evidence that isozymes, and perhaps other molecular polymorphisms, are directly involved in adaptedness will be also presented. Molecular genetic analyses at gene and population levels are opening the ways to a better understanding of plant genetic adaptation.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Aarssen L.W. & S.M. Burton, 1990. Maternal effects at four levers in Senecio vulgaris (Asteraceae) grown on a soil nutrient gradient. Am J Bot 77: 1231–1240.

    Google Scholar 

  • Al-Hiyaly S.A.K., T.M. McNeilly & A.D. Bradshaw, 1990. The effect of zinc contamination from electricity pylons. Contrasting patterns of evolution in five grass species. New Phytol 114: 183–190.

    Google Scholar 

  • Al-Khatib M., T. McNeilly & J.C. Collins, 1993. The potential of selection and breeding for improved salt tolerance in luceme (Medicago sativa L.). Euphytica 65: 43–51.

    Google Scholar 

  • Allard R.W., 1988. Genetic changes associated with the evolution of adaptedness in cultivated plants and their progenies. J Hered 79: 225–238.

    Google Scholar 

  • Allard R.W., P. García, L.E. Sáenz de Miera & M. Pérez de la Vega, 1993. Evolution of multilocus structure in Avena hirtula and Avena barbata. Genetics 135: 1125–1139.

    Google Scholar 

  • Allard R.W., Q. Zhang, M.A. Shagai Maroof & O.M. Mouna, 1992. Evolution of multilocus genetic structure in an experimental barley population. Genetics 1131: 957–969.

    Google Scholar 

  • Bergmann F. & H.R. Gregorius, 1993. Ecogeographical distribution and thermostability of isocitrate dehydrogenase (IDH) allozymes in European silver Fir (Abies alba). Biochem Syst Ecol 21: 5–605.

    Google Scholar 

  • Bradshaw A.D., 1965. Evolutionary significance of phenotypic plasticity in plants. Adv Genet 13: 115–153.

    Google Scholar 

  • Burke J.J., 1990. High temperature stress and adaptation in crops. In: R.G. Alscher & J.R. Cummings (Eds). Stress Responses in Plants: Adaptation and acclimatation mechanisms, pp. 295–309. Wiley-Liss, New York.

    Google Scholar 

  • Burke J.J., J.R. Mahan & J.L. Hatfield, 1988. Crop-specific thermal kinetic windows in relation to wheat and cotton biomass production. Agron J 80: 553–556.

    Google Scholar 

  • Chalmers K.J., R. Waugh, J. Watters, B.P. Foster, E. Nevo, R.J. Abbott & W. Powell, 1992. Grain isozyme and ribosomal DNA variability in Hordeum spontaneum populations from Israel. Theor Appl Genet 84: 313–322.

    Google Scholar 

  • Chanway C.P. & F.B. Holl, 1992. Influence of soil biota on Douglasfir (Pseudotsuga menziesii) seedling growth: the role of rhizosphere bacteria. Can J Bot 70: 1025–1031.

    Google Scholar 

  • Chanway C.P. & L.M. Nelson, 1990. Field and laboratory studies of Triticum aestivum L. inoculated with co-existent growth-promoting Bacillus strains. Soil Biol Biochem 22: 789–795.

    Google Scholar 

  • Chanway C.P., R. Turkington & F.B. Holl, 1991. Ecological implications of specificity between plants and rhizosphere microorganisms. Adv Ecol Res 21: 121–169.

    Google Scholar 

  • Cluster P.D. & R.W. Allard, 1995. Evolution of ribosomal DNA (rDNA) genetic structure in colonial Californian populations of Avena barbata. Genetics 139: 941–954.

    Google Scholar 

  • Davy A.J., S.M. Noble & R.P. Oliver, 1990. Genetic variation and adaptation to flooding in plants. Aqua Bot 38: 91–108.

    Google Scholar 

  • Dubuc M., L. Lapointe & J.-P. Simon, 1988. Kinetic properties of NADP+-malic enzyme in two populations of the C4 weed species Echinochloa crus-galli (L.) Beauv. (Poaceae) from sites of contrasting climates. Funct Ecol 2: 353–362.

    Google Scholar 

  • Emery R.N.J., C.C. Chinnappa & J.G. Chmielewski, 1994. Specialization, plant strategies, and phenotypic plasticity in populations of Stellaria longipes along an elevationl gradient. Int J Plant Sci 155: 203–219.

    Google Scholar 

  • Erskine W., A. Hussain, M. Tahir, A. Bahksh, R.H. Ellis, R.J. Summerfield & E.H. Roberts, 1994. Field evaluation of a model of photothermal flowering responses in a world lentil collection. Theor Appl Genet 88: 423–428.

    Google Scholar 

  • Funk C.R., F.C. Belanger & J.A. Murphy, 1994. Role of endophytes in grasses used for turf and soil conservation. In: C.W. Bacon & J.F. White (Eds). Biotechnology and Endophytic Fungi of Grasses, pp. 201–209. CRC Press, Boca Raton, Florida.

    Google Scholar 

  • García P., F.J. Vences, M. Pérez de la Vega & R.W. Allard, 1989. Allelic and genotypic composition of ancestral Spanish and colonial Californian gene pools of Avena barbata: Evolutionary implications. Genetics 122: 687–694.

    Google Scholar 

  • Graner A., W.F. Ludwig & A.E. Melchinger, 1994. Relationships among European barley germplasm: II. Comparison of RFLP and pedigree data. Crop Sci 34: 1199–1205.

    Google Scholar 

  • Hällgren J.-E. & G. Oquist, 1990. Adaptations to low temperatures. In: R.G. Alscher & J.R. Cumming (Eds). Stress Response in Plants: Adaptation and acclimation mechanisms, pp. 265–293. Wiley-Liss, New York.

    Google Scholar 

  • Hedrick P.W. & L. Holden, 1979. Hitch-hiking: An alternative to coadaptation for the barley and slender wild oat examples. Heredity 43: 79–86.

    Google Scholar 

  • Hoffman A.A. & P.A. Parsons, 1991. Evolutionary genetics and environmental stress. Oxford Sci Publ, Oxford.

    Google Scholar 

  • Kato K. & H. Yokoyama, 1992. Geographical variation in heading characters among wheat landraces, Triticum aestivum L., and its implication for the adaptability. Theor Appl Genet 84: 259–265.

    Google Scholar 

  • Macnair M.R., 1991. Why the evolution of resistance to anthropogenic toxins normally involves major gene changes: the limits to natural selection. Genetica 84: 213–219.

    Google Scholar 

  • McArthur J.V., D.A. Kovacic & M.H. Smith, 1988. Genetic diversity in natural populations of a soil bacterium across a landscape gradient. Proc Natl Acad Sci USA 85: 9621–9624.

    Google Scholar 

  • McNeilly T., 1990. Selection and breeding for salinity tolerance in crop species. A case for optimism? Acta Oecol 11: 595–610.

    Google Scholar 

  • Meharg A.A., Q.J. Cumbes & M.R. Macnair, 1993. Pre-adaptation of Yorkshire fog, Holcus lanatus. L. (Poaceae) to arsenate tolerance. Evolution 47: 313–316.

    Google Scholar 

  • Melchinger A.E., A. Graner, M. Singh & M.A. Messmer, 1994. Relationships among European barley germplasm: I. Genetic diversity among winter and spring cultivars revealed by RFLPs. Crop Sci 34: 1191–1199.

    Google Scholar 

  • Nevo E., A. Ordentlich, A. Beiles & I. Raskin, 1992. Genetic divergence of heat production within and between the wild progenitor of wheat and barley: evolutionary and agronomical implications. Theor Appl Genet 84: 958–962.

    Google Scholar 

  • O'Donoughue L.S., E. Souza, S.D. Tanksley & M.E. Sorrells, 1994. Relationships among North American oat cultivars based on restriction fragment length polymorphisms. Crop Sci 34: 1251–1258.

    Google Scholar 

  • Orr H.A. & J.A. Coyne, 1992. The genetics of adaptation: A reassessment. Am Nat 140: 725–742.

    Google Scholar 

  • Palta J.W. & G. Simon, 1993. Breeding potential for improvement of freezing stress resistance: Genetic separation of freezing tolerance, freezing avoidance, and capacity to cold acclimate. In: P.H. Li & L. Christersson (Eds). Advances in Plant Cold Hardiness, pp. 299–310. CRC Press, Boca Raton, Florida.

    Google Scholar 

  • Parsons P.A., 1987. Evolutionary rates under environmental stress. Evol Biol 21: 311–347.

    Google Scholar 

  • Pérez de la Vega M., P. García & R.W. Allard, 1991. Multilocus genetic structure of ancestral Spanish and colonial Californian populations of Avena barbata. Proc Natl Acad Sci USA 88: 1202–1206.

    Google Scholar 

  • Pérez de la Vega M., L.E. Sáenz de Miera & R.W. Allard, 1994. Ecogeographical distribution and differentiation of multilocus allelic association in Spanish Avena sativa L. Theor Appl Genet 88: 56–64.

    Google Scholar 

  • Platenkamp G.A.J., 1990. Phenotypic plasticity and genetic differentiation in the demography of the grass Anthoxanthum odoratum. J Ecol 78: 772–788.

    Google Scholar 

  • Roberts E., R. Summerfield, R. Ellis & A. Qi, 1993. Adaptation of flowering in crops to climate. Outlook Agric 22: 105–110.

    Google Scholar 

  • Royo C., A. Rodríguez & I. Romagosa, 1993. Differential adaptation of complete and substituted Triticale. Plant Breeding 111: 113–119.

    Google Scholar 

  • Saghai-Maroof M.A., R.W. Allard & Q. Zhang, 1990. Genetic diversity and ecogeographical differentiation among ribosomal DNA alleles in wild and cultivated barley. Proc Natl Acad Sci USA 87: 8486–8490.

    Google Scholar 

  • Shannon M.C., 1985. Principles and strategies in breeding for higher salt tolerance. Plant Soil 89: 227–241.

    Google Scholar 

  • Shonnard G.C. & P. Gepts, 1994. Genetics of heat tolerance during reproductive development in common bean. Crop Sci 34: 1168–1175.

    Google Scholar 

  • Simon J.-P., 1979. Adaptation and acclimatation of higher plants at the enzyme level: Latitudinal variations of thermal properties of NAD malate dehydrogenase in Lathyrus japonicus Willd. (Leguminosae). Oecologia 39: 273–287.

    Google Scholar 

  • Snaydon R.W. & T.M. Davies, 1994. Rapid divergence of plant populations in response to recent changes in soil conditions. Evolution 36: 289–297.

    Google Scholar 

  • Stettler R.F. & H.D. Bradshaw, 1994. The choice of genetic material for mechanistic studies of adaptation in forest trees. Tree Physiol 14: 781–796.

    Google Scholar 

  • Turner A.P., 1994. The responses of plant to heavy metals. In: S.M. Ross (Ed). Toxic metals in soil-plant systems, pp. 153–187. John Wiley and Sons, Chichester.

    Google Scholar 

  • Turner L.B., C.J. Pollock & G.O. Edmeades, 1994. Thermal kinetics of glutathione reductase and their relation to thermotolerance in diverse cultivars in maize. Ann Bot 74: 254–250.

    Google Scholar 

  • van Tienderen P.H. & J.van der Toorn, 1991a. Genetic differentiation between populations of Plantago lanceolata. I. Local adaptation in three contrasting habitats. J Ecol 79: 27–42.

    Google Scholar 

  • van Tienderen P.H. & J.van der Toorn, 1991b. Genetic differentiation between populations of Plantago lanceolata. II. Phenotypic selection in a transplant experiment in three contrasting habitats. J Ecol 79: 43–59.

    Google Scholar 

  • Via S., 1994. The evolution of phenotypic plasticity: What do we really know? In: L.A. Real (Ed). Ecological Genetics, pp. 33–57. Princeton Univ Press, Princeton, New Jersey.

    Google Scholar 

  • Yamaguchi-Shinozaki K. & K. Shinozaki, 1994. A novel cis-acting element in an Arabidopsis gene is involved in responsiveness to drought, low temperature, or high-salt stress. Plant Cell 6: 251–264.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Pérez de la Vega, M. Plant genetic adaptedness to climatic and edaphic environment. Euphytica 92, 27–38 (1996). https://doi.org/10.1007/BF00022825

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00022825

Key words

Navigation