Skip to main content
Log in

Leaf life spans in wild perennial herbaceous plants: a survey and attempts at a functional interpretation

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

Summary

Leaf longevity in 29 herbaceous plant species of Central Europe was studied by inspecting tagged leaves at weekly intervals. About half of the species are elements of the lowland meadow flora, the other half comprises a representative sample of species from the highest sites where vascular plants grow in the Alps. Shaded and water-stressed sites were avoided. Overall mean leaf longevity did not differ significantly between sites and amounted to 71±5 days at low and 68±4 days at high altitude. Leaf life spans ranged (with no clear altitudinal trend) from 41 to 95 days. Low-altitude forbs and grasses produced several leaf cohorts during their growth period, while most alpine species produced only one. Correlations were found between leaf duration and percent nitrogen content and carbon-cost/carbon-gain ratios, but not with leaf dry mass per unit leaf area and photosynthetic capacity alone. As leaf life spans increase, more C tends to be invested per unit CO2 uptake and less N is invested per unit invested C. Thus, mass relationships rather than area relationships seem to be linked to leaf life span in these species, suggesting that leaf duration is associated with properties other than the efficiency of light utilization (e.g. mechanical strength, herbivory or pathogen resistance). It seems that the explanations of leaf duration that have been developed for evergreen/deciduous plants and for plants along steep light gradients do not apply to the variable life spans in leaves of perennial herbaceous plants of open habitats.

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

  • Bahn M, Körner Ch (1987) Vegetation und Phänologie der hochalpinen Gipfelflur des Glungezer in Tirol. Ber Nat-Med Ver Innsbruck 74:61–80

    Google Scholar 

  • Bazzaz FA, Harper JL (1977) Demographic analysis of the growth of Linum usitatissimum. New Phytol 78:193–208

    Google Scholar 

  • Chabot BF, Hicks DJ (1982) The ecology of leaf life spans. Annu Rev Ecol Syst 13:229–259

    Google Scholar 

  • Chapin FS, Schulze ED, Mooney HA (1990) The ecology and economics of storage in plants. Annu Rev Ecol Syst 21: 423–447

    Google Scholar 

  • Diemer MW (1990) Die Kohlenstoffbilanz von Blättern krautiger Pflanzen aus dem Hochgebirge und der Niederung. PhD thesis, Univ Innsbruck

  • Fliri F (1975) Das Klima der Alpen im Raume von Tirol. Univ Verlag Wagner, Innsbruck

    Google Scholar 

  • Harper JL (1989) The value of a leaf. Oecologia 80:53–58

    Google Scholar 

  • Hirose T, Werger MJA (1987) Maximizing daily canopy photosynthesis with respect to the leaf nitrogen allocation pattern in the canopy. Oecologia 72:520–526

    Google Scholar 

  • Hodanova D (1981) Photosynthetic capacity, irradiance and sequential senescence of sugar beet leaves. Biol Plant (Prag) 23:58–67

    Google Scholar 

  • Jurik TW (1983) Reproductive effort and dynamics of wild strawberry populations. Ecology 64:1329–1342

    Google Scholar 

  • Jurik TW, Chabot BF (1986) Leaf dynamics and profitability in wild strawberries. Oecologia 69:296–304

    Google Scholar 

  • Karlsson PS (1985) Effects of water and mineral nutrient supply on a deciduous and an evergreen dwarf shrub: Vaccinium uliginosum L. and V. vitis-idea L. Holarct Ecol 8:1–8

    Google Scholar 

  • Koike T (1988) Leaf structure and photosynthetic performance as related to the forest succession of deciduous broad-leaved trees. Plant Spec Biol 3:77–87

    Google Scholar 

  • Körner Ch (1984) Auswirkungen von Mineraldünger auf alpine Zwergsträucher. Verh Ges Ökol 12:123–136

    Google Scholar 

  • Körner Ch (1989) The nutritional status of plants from high altitudes. A worldwide comparison. Oecologia 81:379–391

    Google Scholar 

  • Körner Ch, Diemer M (1987) In situ photosynthetic responses to light, temperature and carbon dioxide in herbaceous plants from low and high altitude. Funct Ecol 1:179–194

    Google Scholar 

  • Körner Ch, Pelaez Menendez-Riedl S (1989) The significance of developmental aspects in plant growth analysis. In: Lambers H et al. (eds) Causes and consequences of variation in growth rate and productivity of higher plants. SPB Acad Publ, The Hague, pp 141–157

    Google Scholar 

  • Körner Ch, Neumayer M, Pelaez Menendez-Riedl S, Smeets-Scheel A (1989) Functional morphology of mountain plants. Flora 182:353–383

    Google Scholar 

  • Larcher W (1963) Die Leistungsfähigkeit der CO2-Assimilation höherer Pflanzen unter Laboratoriumsbedingungen und am natürlichen Standort. Mitt Florist-Soziol Arbeitsgem N.F. 10:20–33

    Google Scholar 

  • Maillette L (1986) Canopy development, leaf demography and growth dynamics of wheat and three weed species growing in pure and mixed stands. J Appl Ecol 23:929–944

    Google Scholar 

  • Miller PC, Stoner WA (1979) Canopy structural and environmental interactions. In: Solbrig OT et al. (eds) Topics in plant population biology, Columbia Univ Press, New York, pp 428–458

    Google Scholar 

  • Mitchley J (1988) Control of relative abundance of perennials in chalk grassland in Southern England. III. Shoot phenology. J Ecol 76:607–616

    Google Scholar 

  • Mooney HA, Gulmon SL (1982) Constraints on leaf structure and function in reference to herbivory. BioScience 32:198–206

    Google Scholar 

  • Moore DM (1982) Flora Europaea check-list and chromosome index. Cambridge Univ Press, Cambridge

    Google Scholar 

  • Peters B (1980) The demography of leaves in a permanent pasture. PhD thesis, Univ of Wales

  • Reich PB (1987) Quantifying plant response to ozone: a unifying theory. Tree Physiol 3:63–91

    Google Scholar 

  • Schmid B (1985) Clonal growth in grassland perennials. II. Growth form and fine-scale colonizing ability. J Ecol 73:809–818

    Google Scholar 

  • Schulze ED, Fuchs M, Fuchs MI (1977) Spatial distribution of photosynthetic capacity and performance in a mountain spruce forest of Northern Germany. Oecologia 30:239–248

    Google Scholar 

  • Schulze W, Schulze ED (1990) Insect capture and growth of the insectivorous Drosera rotundifolia L. Oecologia 82:427–429

    Google Scholar 

  • Shaver GR (1983) Mineral nutrition and leaf longevity in Ledum palustre: the role of individual nutrients and the timing of leaf mortality. Oecologia 56:160–165

    Google Scholar 

  • Southwood TRE, Brown VK, Reader PM (1986) Leaf palatability, life expectancy and herbivore damage. Oecologia 70:544–548

    Google Scholar 

  • Sydes CL (1984) A comparative study of leaf demography in limestone grassland. J Ecol 72:331–345

    Google Scholar 

  • Van Keulen H, Goudriaan J, Seligman NG (1989) Modelling the effects of nitrogen on canopy development and crop grwoth. In: Russell G, Marshall B, Jarvis PG (eds) Plant canopies: their growth, form and function. (soc Exp Biol Sem Ser 31) Cambridge Univ Press, pp 83–104

  • Williams K, Field CB, Mooney HA (1989) Relationships among leaf construction cost, leaf longevity, and light environment in rain-forest plants of the genus Piper. Am Nat 133: 198–211

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Diemer, M., Körner, C. & Prock, S. Leaf life spans in wild perennial herbaceous plants: a survey and attempts at a functional interpretation. Oecologia 89, 10–16 (1992). https://doi.org/10.1007/BF00319009

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00319009

Key words

Navigation