Skip to main content
Log in

Leaf mass per area relationships across light gradients in hybrid spruce crowns

  • Original Article
  • Published:
Trees Aims and scope Submit manuscript

Abstract

This study examined the distribution and variation of mass to projected area ratio of foliage (LMA, g/m2) within hybrid spruce (Picea engelmannii Parry×Picea glauca (Moench) Voss×Picea sitchensis (Bong.) Carr) crowns across three stages of stand development (20, 60, and 140 years). Variability of LMA was assessed at different heights and branch positions. LMA decreased with distance from top of tree (p<0.0001) at rates that varied among stand development stages (p<0.0001). A multi-level mixed effect analysis indicated that distance from the tip of the first-order branch (p=0.0002) had a significant influence on LMA. In general, LMAs decreased towards the base of the tree and increased towards tree apex.

LMA differed significantly across stand development stages. Older trees (140 years) showed the highest LMA, while younger trees (20 years) showed the lowest LMA values. LMA also increased with foliage age, suggesting a developmental change in leaf area and mass with increasing foliage age. Multiple linear regression (MLR) relationships were developed to predict LMA at various positions within tree crowns. The precision of the models was slightly greater when branch position (from the apex of the tree) was described relative to tree height, rather than relative to crown length. The MLR function resulted in precise representations of LMA within tree crowns.

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.

Institutional subscriptions

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  • Apple M, Tiekotter K, Snow M, Young J, Soeldner A, Phillips D, Tingey DG, Bond BJ (2002) Needle anatomy changes with increasing tree age in Douglas-fir. Tree Physiol 22:129–136

    PubMed  Google Scholar 

  • Ashton PMS, Olander LP, Berlyn GP, Thadani R, Cameron IR (1998) Changes in leaf structure in relation to crown position and tree size of Betula papyrifera within fire-origin stands of interior cedar-hemlock. Can J Bot 76:1180–1187

    Article  Google Scholar 

  • Baldocchi DD (1993) Scaling water vapour and carbon dioxide exchange from leaves to canopy: rules and tools. In: Ehleringer JR, Filed CB (eds) Scaling physiological processes: leaf to globe. Academic, San Diego, pp 77–114

    Google Scholar 

  • Barker MG, Booth WE (1996) Vertical profiles in a Brunei rain forest: II. Leaf characteristics of Dryobalanops lanceolata. J Trop For Sci 9:52–66

    Google Scholar 

  • Billow C, Matson PG,Yoder B (1994) Seasonal biochemical changes in coniferous forest canopies and their response to fertilization. Tree Physiol 14:563–574

    PubMed  Google Scholar 

  • Bjorkman O (1981) Responses to different quantum flux densities. In: Lange OL, Nobel PS, Osmond CB, Ziegler H (eds) Physiological plant ecology I. Responses to the physical environment. Springer-Verlag, Berlin Heidelberg New York, pp 57–107

  • Bond JB, Farnsworth BT, Coulombe RA, Winner WE (1999) Foliage physiology and biochemistry in response to light gradients in conifers with varying shade tolerance. Oecologia 120:183–192

    Article  Google Scholar 

  • Brooks JR, Hinkley TM, Ford ED, Sprugel DG (1991) Foliage dark respiration in Abies amabilis (Dougl.) Forbes: variation within the canopy. Tree Physiol 9:325–338

    PubMed  Google Scholar 

  • Brooks JR, Schulte PJ, Bond BJ, Coulombe R, Domec JC, Hinkley TM, McDowell N, Phillips N (2003) Does foliage on the same branch compete for the same water? Experiments on Douglas-fir trees. Trees 17:101–108

    Google Scholar 

  • Chabot BF, Jurik TW, Chabot JF (1979) Influence of instantaneous and integrated light-flux density on leaf anatomy and photosynthesis. Am J Bot 66:940–945

    Article  Google Scholar 

  • Clement CJ, Banner A (1992) Ecosystem mapping of the Date Creek silvicultural systems research area, Prince Rupert Forest Region. Report to the BC Ministry of Forests, Victoria, 33 pp

  • Ellsworth DS, Reich PB (1993) Canopy structure and vertical patterns of photosynthesis and related leaf traits in a deciduous forest. Oecologia 96:169–178

    Article  Google Scholar 

  • Farquhar GD, O’Leary MH, Berry JA (1982) On the relationship between carbon isotope discrimination and the intercellular carbon dioxide concentration in leaves. Aust J Plant Physiol 9:121–137

    Article  CAS  Google Scholar 

  • Gertner GG, Kohl M (1995) Correlated observer errors and their effects on survey estimates of needle-leaf loss. For Sci 41:758–776

    Google Scholar 

  • Gilmore DW, Seymour RS, Halteman WA, Greenwood MS (1995) Canopy dynamics and the morphological development of Abies balsamea: effects of foliage age on specific leaf area and secondary vascular development. Tree Physiol 15:47–55

    Article  PubMed  Google Scholar 

  • Goldfeld SM, Quandt RE (1965) Some tests for homoscedasticity. J Am Stat Assoc 60:539–547

    Article  Google Scholar 

  • Grulke NEG, Miller PR (1994) Changes in gas exchange characteristics during the life span of giant sequoia: implications for response to current and future concentrations of atmospheric ozone. Tree Physiol 14:659–668

    PubMed  CAS  Google Scholar 

  • Gulmon SLG, Chu CC (1981) The effects of light and nitrogen on photosynthesis, leaf characteristics, and dry matter allocation in the chaparral shrub, Diplacus aurantiacus. Oecologia 49:207–212

    Article  Google Scholar 

  • Gutschick VPG, Weigel FW (1988) Optimizing the canopy photosynthetic rate by patterns of investments in specific leaf mass. Am Nat 132:68–85

    Article  Google Scholar 

  • Hollinger DY (1989) Canopy organization and foliage photosynthetic capacity in a broad-leaved evergreen montane forest. Funct Ecol 3:53–62

    Article  Google Scholar 

  • Jarvis PG (1993) Prospects for bottom-up models. In: Ehleringer JR, Filed CB (eds) Scaling physiological processes: leaf to globe. Academic, San Diego, pp 115–126

    Google Scholar 

  • Judge GC, Griffith WE, Hill RC, Lutkephol H, Lee T (1985) The theory and practice of econometrics, 2nd edn. Wiley, Toronto, 1019 pp

    Google Scholar 

  • Landsberg JJG, Waring RH (1997) A generalized model of forest productivity using simplified concepts of radiation use efficiency, carbon balance and partitioning. For Ecol Manage 95:209–228

    Article  Google Scholar 

  • Marshall JD, Monserud RA (2003) Foliage height influences specific leaf area of three conifer species. Can J For Res 33:164–170

    Article  Google Scholar 

  • Meidinger D, Pojar J (1991) Ecosystems of British Columbia. Research Branch, British Columbia Ministry of Forests, Victoria, BC, 330 pp

  • Nageswara Rao RCG, Wright GC (1994) Stability of the relationship between specific leaf area and carbon isotope discrimination across environment in peanut. Crop Sci 34:98–103

    Google Scholar 

  • Neter J, Wasserman W, Kutner MH (1990) Applied linear statistical models. IRWIN, MA, 1181 pp

    Google Scholar 

  • Oberbauer SFG, Strain BR (1986) Effects of canopy position and irradiance on the leaf physiology and morphology of pentaclethra macroloba (mimosaceae). Am J Bot 73:409–416

    Article  Google Scholar 

  • Oren R, Schulze E-D, Matyssek RG, Zimmermann R (1986) Estimating photosynthetic rate and annual carbon gain in conifers from specific leaf weight and leaf biomass. Oecologia 70:187–193

    Article  Google Scholar 

  • Parker GG, Davis MM, Chapotin SM (2002) Canopy light transmittance in Douglas-fir—western hemlock stands. Tree Physiol 22:147–158

    PubMed  Google Scholar 

  • Pinheiro JCG, Bates DM (2000) Mixed-effects models in S and S-Plus. Springer, Berlin Heidelberg New York, 528 pp

    Google Scholar 

  • Reich PB, Walters MB, Ellsworth DS (1997) From tropics to tundra: global convergence in plant functioning. Proc Natl Acad Sci USA 94:13730–13734

    Article  PubMed  CAS  Google Scholar 

  • Richardson AD, Berlyn GP, Ashton PMS, Thadani R, Cameron IR (2000) Foliar plasticity of hybrid spruce in relation to crown position and stand age. Can J Bot 78:305–317

    Article  Google Scholar 

  • Running SWG, Coughlan JC (1988) A general model of forest ecosystem processes for regional applications. I. Hydrologic balance, canopy gas exchange and primary production processes. Ecol Modell 41:125–154

    Article  Google Scholar 

  • SAS Institute Inc. (1989) SAS/STAT users's guide, version 6, vol. 2, 4th edn. SAS Institute Inc., Cary, NC, 846 pp

    Google Scholar 

  • Schoettle AW (1994) Influence of tree size on shoot structure and physiology of Pinus contorta and Pinus aristata. Tree Physiol 14:1055–1068

    PubMed  Google Scholar 

  • Schulze ED, Fuchs MI, Fuchs M (1977) Spatial distribution of photosynthetic capacity and performance in a mountain spruce forest of Northern Germany. I. Biomass distribution and daily CO2 uptake in different crown layers. Oecologia 29:43–61

    Article  Google Scholar 

  • Shapiro SS, Wilk MB (1965) An analysis of variance test for normality (complete samples). Biometrika 52:591–611

    Article  Google Scholar 

  • Sutton BCS, Pritchard SC, Gawley JR, Newton CH, Kiss GK (1994) Analysis of Sitka spruce–interior spruce introgressions in British Columbia using cytoplasmic and nuclear DNA probes. Can J For Res 24:278–285

    Article  Google Scholar 

  • Temesgen H (2003) Evaluation of sampling alternatives to quantify tree leaf area. Can J For Res 33:82–95

    Article  Google Scholar 

  • Vitousek PM, Field CB, Matson PA (1990) Variation in foliar δ13C in Hawaiian Metrosideros polymorpha: a case of internal resistance? Oecologia 84:362–370

    Google Scholar 

  • Wang YP, Jarvis PG, Benson ML (1990) Two dimensional needle-area density distribution within the crowns of Pinus radiata. For Ecol Manage 32:217–237

    Article  Google Scholar 

  • Webb WL, Ungs JM (1993) Three dimensional distribution of needle and stem surface area in a Douglas-fir crown. Tree Physiol 13:203–212

    PubMed  Google Scholar 

  • Weinbaum SW, Southwick SM, Shackel KA, Muraoka TT, Krueger WG, Yeager JT (1989) Photosynthetic photon flux influences microelement weight and leaf dry weight per unit of area in prune tree canopies. J Am Soc Hortic Sci 114:720–723

    Google Scholar 

  • Woodman JN (1971) Variation of net photosynthesis within the crown of a large forest-grown conifer. Photosynthetica 5:50–54

    Google Scholar 

  • Woodruff DR, Bond BJ, Meinzer FC (2004) Does turgor limit growth in tall trees? Plant Cell Environ 27:229–236

    Article  Google Scholar 

  • Yoder BJ, Ryan MG, Waring RH, Schoettle AW, Kaufmann MR (1994) Evidence of reduced photosynthetic rates in old trees. Forest Sci 40:513–527

    Google Scholar 

Download references

Acknowledgements

The financial support of the British Columbia (BC) Ministry of Forests, Research Branch and the Department of Forest Resources at Oregon State University for the analysis phase of this research is gratefully acknowledged. We thank Drs. B. Bond, V. LeMay, and Robert Monserud for their comments on earlier drafts, and I. R. Cameron for coordinating the data collection phase of this study. We thank the two anonymous referees and the Communicating Editor for their constructive comments and insights.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to H. Temesgen.

Additional information

Communicated by M. Adams

Rights and permissions

Reprints and permissions

About this article

Cite this article

Temesgen, H., Weiskittel, A.R. Leaf mass per area relationships across light gradients in hybrid spruce crowns. Trees 20, 522–530 (2006). https://doi.org/10.1007/s00468-006-0068-0

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00468-006-0068-0

Keywords

Navigation