| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Annals of Botany 72: 165-172, 1993
© 1993 Annals of Botany Company
The Scaling of Plant Height: A Comparison Among Major Plant Clades and Anatomical Grades
Section of Plant Biology, Cornell University, Ithaca, New York 14853, USA
The scaling plant height h (m) with respect to stem diameter d (m) was determined for a total 610 species (mosses, n = 40; pteridophytes, n = 16; dicotyledonous herbs, n = 117; palms, n = 17; gymnosperms, n = 105; dicotyledonous trees, n = 315); axial length or mass vs. d was determined for the pteridophyte Psilotum nudum ; and the scaling of critical buckling height hcrit of gymnosperm and dicotyledonous trees was calculated based on the record trunk d and average Young's modulus E and density p of 33 wood species. The scaling exponents (based on least squares and reduced major axis regressions;
LS and
RMA, respectively) of these relations were compared to expected values for three scaling models: elastic similarity,
= 0·666; stress similarity,
= 0·500; and geometric similarity,
= 1·00. Least squares regression of the data from all species yielded h = 22 d0·91 (r2 = 0·955, n = 610;
RMA = 0·93). The scaling exponent of this formula complied best with the geometric similarity model (
1·00). However,
differed among plant clades and anatomical grades: mosses,
LS = 1·10 (r2 = 0·974;
RMA = 1·12); pteridophytes,
LS = 1·69 (r2 = 0·847;
RMA = 1·83; herbaceous dicotyledons,
LS = 1·26 (r2 = 0·742;
RMA = 1·46); palms,
LS = 1·76 (r2 = 0·940;
RMA = 1·82); gymnosperm trees,
LS = 0·430 (r2 = 0·247;
RMA = 0·87); dicotyledonous trees,
LS = 0·488 (r2 = 0·515;
RMA = 0·69); woody species (gymnosperm and dicotyledonous trees,
LS = 0·538 (r2 = 0·541;
RMA = 0·73); and non-woody species,
LS = 1·29 (r2 = 0·949;
RMA = 1·32). Based on
RMA, the interspecific scaling of woody species complied neither with the stress or elastic similarity model. Regression of hcrit yielded the formula hcrit = 97·7 d0·689 (r2 = 0·969;
RMA = 0·70), which was interpreted to support the assumption that E/p
a constant among gymnosperm and dicotyledonous woods. Intra- and interspecific variations in
RMA caution against using any of the three scaling models to predict h based on d across a broad taxonomic spectrum of species, although, on the average,
RMA < 1·0 and
RMA > 1·0 for woody and non-woody species, respectively.Copyright 1993, 1999 Academic Press
Plant allometry, biomechanics, trees
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
M. Brea and A. F. Zucol Guadua zuloagae sp. nov., the First Petrified Bamboo Culm Record from the Ituzaingo Formation (Pliocene), Parana Basin, Argentina Ann. Bot., October 1, 2007; 100(4): 711 - 723. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. S. WATT, J. R. MOORE, J.-P. FACON, G. M. DOWNES, P. W. CLINTON, G. COKER, M. R. DAVIS, R. SIMCOCK, R. L. PARFITT, J. DANDO, et al. Modelling Environmental Variation in Young's Modulus for Pinus radiata and Implications for Determination of Critical Buckling Height Ann. Bot., October 1, 2006; 98(4): 765 - 775. [Abstract] [Full Text] [PDF] |
||||
![]() |
Z. Hejnowicz and W. Barthlott Structural and mechanical peculiarities of the petioles of giant leaves of Amorphophallus (Araceae) Am. J. Botany, March 1, 2005; 92(3): 391 - 403. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. J. Beerling and R. A. Berner Feedbacks and the coevolution of plants and atmospheric CO2 PNAS, February 1, 2005; 102(5): 1302 - 1305. [Abstract] [Full Text] [PDF] |
||||


