Nothing Special   »   [go: up one dir, main page]

Skip to main content
Log in

Adaptive phenology of desert and Mediterranean populations of annual plants grown with and without water stress

  • Original Papers
  • Published:
Oecologia Aims and scope Submit manuscript

Summary

The dynamics of vegetative and reproductive growth were compared in matched pairs of Mediteranean and desert populations of three unrelated annual species, Erucaria hispanica (L.) Druce, Brachypodium distachyon (L.) Beauv. and Bromus fasciculatus C. Presl., under high and low levels of water availability in a common-environment experiment. Plants of all desert populations showed earlier switches to reproductive development and to subsequent phenophases, and the transition to flowering occurred at smaller plant sizes. Water stress had no effect (E. hispanica) or slightly accelerated the transition to flowering in B. fasciculatus (by 1–2 days) and in B. distachyon (by 4–6 days). Plant senescence was strongly enhanced by water stress, and this enhancement was greater in desert populations than in corresponding Mediterranean ones. Duration of life cycle was greatly shortened by water stress in all three species. Desert and Mediterranean populations of the three species exhibited small differences in their relative response, i.e. phenotypic plasticity, to water stress for phenological and plant size parameters. In E. hispanica and B. fasciculatus the population x water regime interaction amounted to less than 3% of total variance. By contrast, the Mediterranean population of B. distachyon was much more plastic in its response to water stress than the desert population in its transition to plant senescence. Plants from the desert populations appeared to be adapted to shorter, more compact growth cycles, culminating in earlier dates of seed maturation and plant senescence. In addition, they showed larger phenotypic plasticity in the transition to plant senescence, which trait was enhanced or magnified by sustained or repeated lack of water. By contrast, plants from Mediterranean populations delayed switchover from one phenophase to the next, seeming thus to “bet” on more water being forthcoming.

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

Access this article

Subscribe and save

Springer+ Basic
$34.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or eBook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

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

  • Abbot RJ (1976) Variation within common groundsel (Senecio vulgaris L.) I. Genetic responses to spatial variation in the environment. New Phytol 76: 153–164

    Google Scholar 

  • Angus JF, Moncur MW (1977) Water stress and phenology of wheat. Aust J Agric Res 28:177–181

    Google Scholar 

  • Aronson J (1990) Comparison of Life History Strategies in Desert and Mediterranean Populations of Ephemeral Plant Species in Israel. Hebrew University of Jerusalem, Israel

    Google Scholar 

  • Aronson J, Shmida A (1991) Plant species diversity along a Mediterranean-desert gradient and its correlation to interannual variation in rainfall. J Arid Envir, in press

  • Aronson J, Kigel J, Shmida A (1989). Responses to water stress in Mediterranean and desert populations of two annual grasses and a crucifer. In: Di Castri F, Roy J, Floret C, Rambal S (eds), Time Scales and Water Stress, I.U.B.S., Paris, pp 239–245

    Google Scholar 

  • Aronson J, Kigel J, Shmida A (1990) Comparative variability in desert and Mediterranean populations of annual plants in Israel. Israel J Bot 39:413–430

    Google Scholar 

  • Barlow EWR, Munns RE, Brady CJ (1980) Drought responses of apical meristems. In: Turner NC, Kramer PJ (eds) Adaptations of Plants to Water and High Temperature Stress. Wiley, New York, pp 191–205

    Google Scholar 

  • Bradshaw AD (1965) Evolutionary significance of phenotypic plasticity in plants. Adv Genetics 13:115–155

    Google Scholar 

  • Carey K (1983) Breeding systems, genetic variability and response to selection in Plestritis (Valarianeaceae). Evolution 37: 947–956

    Google Scholar 

  • Clarkson NM, Russell JS (1976) Effect of water stress on the plastic development of annual Medicago species. Aust J Agric Res 27: 227–234

    Google Scholar 

  • Cohen D (1971) Maximizing final yield when growth is limited by time or by limiting resources. J Theor Biol 33: 299–307

    Google Scholar 

  • Cohen D (1976) The optimal timing of reproduction. Am Nat 110: 801–807

    Google Scholar 

  • Evenari M, Gutterman Y (1965) The photoperiodic response of some desert plants. Zeits Pflanzenphysiol 54: 7–27

    Google Scholar 

  • Evenari M, Gutterman Y (1985) Desert Plants. In: Halevy AH (ed), CRC Handbook of Flowering Plants. Vol I. CRC Press, Boca Raton, Florida, pp 41–59

    Google Scholar 

  • Evenari M, Shanan L, Tadmor N (1982) The Negev: Challenge of a Desert, 2nd edn. Harvard University, Cambridge, USA

    Google Scholar 

  • Ezcurra R, Rodrigues V (1966) Rainfall patterns in the Gran Desierto, Sonora, Mexico. J Arid Environ 10: 13–28

    Google Scholar 

  • Feinbrun-Dothan N (1986) Flora Palaestina, Vol. 4, Israel Acad Sci & Humanities, Jerusalem

    Google Scholar 

  • Fox GA (1990a) Consequences of flowering time variation in a desert annual: adaptation and history. Ecology 70: 1294–1306

    Google Scholar 

  • Fox GA (1990b) Drought and the evolution of flowering time in desert annuals. Am J Bot 77: 1508–1518

    Google Scholar 

  • Gates CT (1968) Water deficits and growth of herbaceous plants. In: Kozlowski TT (ed) Water Deficits and Plant Growth, Vol. 2. Plant Water Consumption and Response. Academic Press, New York, pp 135–140

    Google Scholar 

  • Hedge IC, Lamond JC (1980) In: Townsend CC, Guest E (eds) Flora of Iraq. Vol. 4 Part 2. Min Agric and Agrarian Reform, Baghdad

    Google Scholar 

  • Hickman JC (1975) Environmental unpredictability and plastic energy allocation strategies in the annual Polygonum cascadense (Polygonaceae). J Ecol 63: 689–702

    Google Scholar 

  • Hickman JC (1977) Energy allocation and niche differentiation in four co-existing annual species of Polygonum in western North America. J Ecol 65: 317–326

    Google Scholar 

  • Jain S (1978) Adaptive strategies: polymorphism, plasticity and homeostasis. In: Solbrig O (ed) Topics in plant population biology. Columbia Univ Press, New York, pp 160–187

    Google Scholar 

  • Kaderit JW, Briggs D (1985) Speed of development of radiate and non-radiate plants of Senecio vulgaris L. from habitats subject to different degrees of weeding pressure. New Phytol 99: 155–169

    Google Scholar 

  • King D, Roughgarden J (1982) Multiple switches between vegetative and reproductive growth in annual plants. Theor Pop Biol 21: 194–204

    Google Scholar 

  • Lacey EP (1986) Onset of reproduction in plants: Size- versus Age-dependency. Trends Ecol Evol 1: 72–76

    Google Scholar 

  • Lacey EP (1988) Latitudinal variation in reproductive timing of a short-lived monocarp, Daucus carota (Apiaceae). Ecology 69: 220–232

    Google Scholar 

  • Landau N (1957) Effect of length of day and temperature on the development of some annual legumes indigenous to Israel. Bull Res Coun Israel 5: 245–256

    Google Scholar 

  • Law R, Bradshaw AD, Putwain PD (1977) Life history variation in Poa annua. Evolution 31: 3–16

    Google Scholar 

  • Le Houerou HN (1984) Rain use efficiency: a unifying concept in arid-land ecology. J Arid Environ 7: 213–247

    Google Scholar 

  • Levins R (1963) Theory of fitness in a heterogenous environment II. Developmental flexibility and niche selection. Am Nat 97: 75–90

    Google Scholar 

  • Lewontin RC (1957) The adaptations of populations to varying environments. Cold Spring Harbor Symp Quant Biol 22: 395–408

    Google Scholar 

  • MacWilliams EC, Landers PR, Mahlstede JP (1967) Ecotypic differentiation in response to photoperiodism in several species of Amaranthus. Iowa Acad Sc Proc, 1966, 2 p

  • Newman EI (1965) Factors affecting seed production of Teesdalia nudicaulis. II. Soil moisture in spring. J Ecol 53: 211–232

    Google Scholar 

  • Neuffer B (1990) Ecotypic differentiation in Capsella. Vegetatio 89: 165–171

    Google Scholar 

  • Paltridge GW, Denholm JV (1974) Plant yield and the switch from vegetative to reproductive growth. J Theor Biol 44: 23–34

    Google Scholar 

  • Ray PM, Alexander WE (1966) Photoperiodic adaptation to latitude in Xanthium strumarium. Am J Bot 53: 806–816

    Google Scholar 

  • Rathcke BJ, Lacey EP (1985) Phenological patterns of terrestrial plants. Annu Rev Ecol Syst 16: 179–214

    Google Scholar 

  • Ritland K (1983) The joint evolution of seed dormancy and flowering time in annual plants living in variable environments. Theor Pop Biol 24: 213–243

    Google Scholar 

  • Samson DA, Werk KS (1986) Size-dependent effects in the analysis of reproductive effort in plants. Am Nat 127: 667–680

    Google Scholar 

  • Schaffer WM (1974) The evolution of optimal reproductive strategies: the effects of age structure. Ecology 55: 291–303

    Google Scholar 

  • Schemske DW (1984) Population structure and local selection in Impatiens pallida (Balsaminaceae), a selfing annual. Evolution 38: 817–832

    Google Scholar 

  • Schlichting CD (1986) The evolution of phenotypic plasticty in plants. Annu Rev Ecol Syst 17: 667–693

    Google Scholar 

  • Schmitt J (1983) Individual flowering phenology, plant size and reproductive success in Limnanthes androsaceus, a California annual. Oecologia 59: 135–140

    Google Scholar 

  • Scholz H (1987) Delimitation and classification of Bromus fasciculatus (Poaceae). Plant Syst Evol 155: 277–282

    Google Scholar 

  • Shmida A, Burgess T (1988) Plant growth-form strategies and vegetation types in arid environments. In: Werger MJA, van der Aart PJM, During HJ, Verhoeven JTA (eds) Plant Form and Vegetation Structure. SPB Academic, The Hague, pp 211–242

    Google Scholar 

  • Silvertown JW (1987) Introduction to Plant Population Ecology, 2nd edn. Longman, London

    Google Scholar 

  • Smith PM (1970) Taxonomy and nomenclature of the Brome-grasses (Bromus L. s.1.). Notes Roy Bot Gard Edinburgh 30: 361–375

    Google Scholar 

  • Sorenson T (1954) Adaptation of small plants to deficient nutrition and a short growing season illustrated by cultivation experiments with Capsella bursa-pastoris L. Med Botanisk Tidesskrift 51: 339–361

    Google Scholar 

  • Stephenson AG (1981) Flower and fruit abortion: proximate causes and ultimate functions. Annu Rev Ecol Syst 12: 253–278

    Google Scholar 

  • Sultan SE (1987) Evolutionary significance of phenotypic plasticity in plants. Evol Biol 21: 127–178

    Google Scholar 

  • Vince-Prue D (1975) Photoperiodism in plants. McGraw Hill, London

    Google Scholar 

  • Went F (1949) Ecology of desert plants. II. The effect of rain and temperature on germination and growth. Ecology 30: 1–13

    Google Scholar 

  • Whiteman PC, Wilson GL (1965) Effects of water stress on the reproductive development of Sorghum vulgare Pers. Univ Queensland Papers 4: 233–239

    Google Scholar 

  • Woolhouse HW (1983) Hormonal control of senescence allied to reproduction in plants. In: Meudt WJ (ed) Strategies of plant reproduction. BARC, Washington DC, pp 201–233

    Google Scholar 

  • Zohary M (1966) Flora Palaestina Vol. 1. Israel Acad Sci & Humanities. Jerusalem, Israel

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Aronson, J., Kigel, J., Shmida, A. et al. Adaptive phenology of desert and Mediterranean populations of annual plants grown with and without water stress. Oecologia 89, 17–26 (1992). https://doi.org/10.1007/BF00319010

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00319010

Key words

Navigation