Skip to main content
Log in

Growth, biomass distribution and CO2 exchange of northern hardwood seedlings in high and low light: relationships with successional status and shade tolerance

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

Abstract

The physiology, morphology and growth of first-year Betula papyrifera Marsh., Betula alleghaniensis Britton, Ostrya virginiana (Mill.) K. Koch, Acer saccharum Marsh., and Quercus rubra L. seedlings, which differ widely in reported successional affinity and shade tolerance, were compared in a controlled high-resource environment. Relative to late-successional, shade-tolerant Acer and Ostrya species, early-successional, shade-intolerant Betula species had high relative growth rates (RGR) and high rates of photosynthesis, nitrogen uptake and respiration when grown in high light. Fire-adapted Quercus rubra had intermediate photosynthetic rates, but had the lowest RGR and leaf area ratio and the highest root weight ratio of any species. Interspecific variation in RGR in high light was positively correlated with allocation to leaves and rates of photosynthesis and respiration, and negatively related to seed mass and leaf mass per unit area. Despite higher respiration rates, early-successional Betula papyrifera lost a lower percentage of daily photosynthetic CO2 gain to respiration than other species in high light. A subset comprised of the three Betulaceae family members was also grown in low light. As in high light, low-light grown Betula species had higher growth rates than tolerant Ostrya virainiana. The rapid growth habit of sarly-successional species in low light was associated with a higher proportion of biomass distributed to leaves, lower leaf mass per unit area, a lower proportion of biomass in roots, and a greater height per unit stem mass. Variation in these traits is discussed in terms of reported species ecologies in a resource availability context.

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

  • Augspurger CK (1984) Seedling survival of tropical tree species: interactions of dispersal distance, light gaps, and pathogens. Ecology 65: 1705–1712

    Google Scholar 

  • Baker FS (1949) A revised tolerance table. J For 47: 179–181

    Google Scholar 

  • Bazzaz FA (1979) The physiological ecology of plant succession. Ann Rev Ecol Syst 10: 351–372

    Google Scholar 

  • Braun EL (1950) Deciduous Forests of Eastern North America. McGraw-Hill Book Co. Inc. New York 596 p

    Google Scholar 

  • Canham C (1988) Growth and canopy architecture of shade tolerant trees: the response of Acer Saccharum and Fagus grandifolia to canopy gaps. Ecology 69: 786–795

    Google Scholar 

  • Canham CD, Denslow JS, Platt WJ, Runkle JR, Spies TA, White PS (1990) Light regimes beneath closed canopies and tree-fall gaps in temperate and tropical forests. Can J For Res 20: 620–631

    Google Scholar 

  • Chapin III FS (1980) The mineral nutrition of wild plants. Annu Rev Ecol Syst 11: 233–260

    Google Scholar 

  • Coley PD (1988) Effects of plant growth rate and leaf lifetime on the amount and type of anti-herbivore defense. Oecologia 74: 531–536

    Google Scholar 

  • Coley PD, Bryant JP, Chapin III FS (1985) Resource availability and plant anti-herbivore defense. Science 230: 895–899

    Google Scholar 

  • Crow TR (1988) Reproductive mode and mechanisms for self replacement of northern red oak (Quercus rubra) — a review. For Sci 34: 19–40

    Google Scholar 

  • Curtis JT (1959) The Vegetation of Wisconsin: An Ordination of Plant Communities. The University of Wisconsin Press 655 p

  • Ellsworth DS, Reich PB (1992) Leaf mass per area, nitrogen content, and photosynthetic carbon gain in Acer saccharum seedlings in contrasting forest light environments. Funct Ecol 6: 423–435

    Google Scholar 

  • Evans GC (1972) The Quantitative Analysis of Plant Growth. University of California Press. 734 p

  • Forcier LK (1975) Reproductive strategies and the co-occurrence of climax tree species. Science 189: 808–809

    Google Scholar 

  • Fowells HA (1965) Silvics of Forest Trees of the United States. United States Department of Agriculture, Agricultural Hand-book Number 271

  • Garnier E (1991) Resource capture, biomass allocation and growth in herbaceous plants. Trends Ecol Evol 6: 126–131

    Google Scholar 

  • Givnish TJ (1988) Adaptation to sun and shade: a whole-plant perspective. Aust J Plant Physiol. 5: 63–92

    Google Scholar 

  • Grime JP (1979) Plant Strategies and Vegetation Processes. John Wiley and Sons, Chichester

    Google Scholar 

  • Grime JP, Jeffery DW (1965) Seedling establishment in vertical gradients of sunlight. J Ecol 53: 621–642

    Google Scholar 

  • Hunt R (1982) Plant Growth Curves. The Functional Approach to Growth Analysis. Edward Arnold, London

    Google Scholar 

  • Huston M, Smith T (1987) Plant succession: life history and competition. Am Nat 130: 168–198

    Google Scholar 

  • Körner C (1991) Some often overlooked plant characteristics as determinants of growth: a reconsideration. Funct Ecol 5: 162–173

    Google Scholar 

  • Korstian CF, Coile TS (1938) Plant competition in forest stands. Duke Univ School For Bull 3. 125 p + 14 plates

  • Kotar J, Kovach JA, Locey CT (1988) Field Guide to Forest Habitat Types of Northern Wisconsin. Department of Forestry, University of Wisconsin-Madison and the Wisconsin Department of Natural Resources

  • Kruger EL (1992) Survival, growth, root:shoot relations and ecophysiology of northern red oak (Quercus rubra L.) and competing tree regeneration in response to fire and related disturbance in mesic forest openings. Ph.D. thesis, University of Wisconsin, Madison

  • Küppers M (1989) Ecological significance of above-ground architectural patterns in woody plants: a question of cost-benefit relationships. TREE 4: 375–379

    Google Scholar 

  • Loach K (1970) Shade tolerance in tree seedlings. II. growth analysis of plants raised under artificial shade. New Phytol 69: 273–286

    Google Scholar 

  • Molofsky J, Augspurger CK (1992) The effect of leaf litter on early seedling establishment in a tropical forest. Ecology 73: 68–77

    Google Scholar 

  • Perala DA, Alm AA (1990) Reproductive ecology of birch: a review. For Ecol Man 32: 1–38

    Google Scholar 

  • Poorter H, Remkes C (1990) Leaf area ratio and net assimilation rate of 24 wild species differing in relative growth rate. Oecologia 83: 553–559

    Google Scholar 

  • Poorter H, Remkes C, Lambers H (1990) Carbon and nitrogen economy of 24 wild species differing in relative growth rate. Plant Physiol 94: 621–627

    Google Scholar 

  • Poorter H, Van der Werf A, Atkin OK, Lambers H (1991) Respiratory energy requirements of roots vary with the potential growth rate of plant species. Physiol Plant 83: 469–475

    Google Scholar 

  • Reich PB, Uhl C, Walters MB and Ellsworth DS (1991) Leaf lifespan as a determinant of leaf structure and function among 23 species in Amazonian forest communities. Oecologia 86: 16–24

    Google Scholar 

  • Reich PB, Walters MB, Ellsworth DS (1992) Leaf lifespan in relation to leaf, plant and stand characteristics among diverse ecosystems. Ecol Monog 62: 365–392

    Google Scholar 

  • Salisbury EJ (1942) The Reproductive Capacity of Plants: Studies in Quantitative Biology, Bell, London

    Google Scholar 

  • Schultze ED, Küppers M, Matyssek R (1986) The roles of carbon balance and branching pattern in the growth of woody species. In: Givnish TJ (ed) On the Economt of Plant Form and Function. Cambridge University Press, New York, pp 585–602

    Google Scholar 

  • Shipley B, Peters RH (1990) The allometry of seed weight and seedling relative growth rate. Func Ecol 4: 523–529

    Google Scholar 

  • Shirley HL (1945) Reproduction of upland conifers in the lake states as affected by root competition and light. Am Mid Nat 33: 537–612

    Google Scholar 

  • Tilman D (1988) Plant Strategies and the Dynamics and Structure of Plant Communities. Princeton University Press, Princeton, NJ

    Google Scholar 

  • Tubbs CH (1977) Managers handbook for northern hardwoods in the north central states. United States Forest Service North Central Forest Experiment Station General Technical Report NC-39

  • Vitousek PM, Matson PA, Van Cleve K (1989) Nitrogen availability and nitrification during succession: primary, secondary, and oldfield seres. In: Clarholm M, Bergstrom L, (eds) Ecology of Arable Land. Kluwer Academic, Amsterdam. pp. 161–171

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Walters, M.B., Kruger, E.L. & Reich, P.B. Growth, biomass distribution and CO2 exchange of northern hardwood seedlings in high and low light: relationships with successional status and shade tolerance. Oecologia 94, 7–16 (1993). https://doi.org/10.1007/BF00317294

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00317294

Key words

Navigation