Ecophysiological responses to light availability in three Blechnum species (Pteridophyta, Blechnaceae) of different ecological breadth

[1]  S. Hall-Aspland,et al.  A new approach to the solution of the linear mixing model for a single isotope: application to the case of an opportunistic predator , 2005, Oecologia.

[2]  E. Gianoli,et al.  Morphological plasticity in response to shading in three Convolvulus species of different ecological breadth , 2004 .

[3]  C. Lusk.  Leaf area and growth of juvenile temperate evergreens in low light: species of contrasting shade tolerance change rank during ontogeny , 2004 .

[4]  R. Montgomery.  Relative importance of photosynthetic physiology and biomass allocation for tree seedling growth across a broad light gradient. , 2004, Tree physiology.

[5]  K. Kitajima.  Relative importance of photosynthetic traits and allocation patterns as correlates of seedling shade tolerance of 13 tropical trees , 1994, Oecologia.

[6]  P. Reich,et al.  Canopy structure and vertical patterns of photosynthesis and related leaf traits in a deciduous forest , 1993, Oecologia.

[7]  R. Chazdon.  Photosynthetic plasticity of two rain forest shrubs across natural gap transects , 1992, Oecologia.

[8]  Hendrik Poorter,et al.  Leaf area ratio and net assimilation rate of 24 wild species differing in relative growth rate , 1990, Oecologia.

[9]  C. Field,et al.  Photosynthetic light acclimation in two rainforest Piper species with different ecological amplitudes , 1987, Oecologia.

[10]  F. A. Bazzaz,et al.  Photosynthetic acclimation to variability in the light environment of early and late successional plants , 1982, Oecologia.

[11]  Influencia de las especies del dosel en la disponibilidad de recursos y regeneración avanzada en un bosque templado lluvioso del sur de Chile , 2003 .

[12]  C. Lusk,et al.  Survival and growth of seedlings of 12 Chilean rainforest trees in two light environments: Gas exchange and biomass distribution correlates , 2002 .

[13]  John R. Evans,et al.  Photosynthetic acclimation of plants to growth irradiance: the relative importance of specific leaf area and nitrogen partitioning in maximizing carbon gain , 2001 .

[14]  E. Molla.  Lack of Differential Plasticity to Shading of Internodes and Petioles with Growth Habit in Convolvulus arvensis (Convolvulaceae) , 2001 .

[15]  C. Canham,et al.  Sapling growth in response to light and nitrogen availability in a southern New England forest , 2000 .

[16]  P. Reich,et al.  Relationships of leaf dark respiration with light environment and tissue nitrogen content in juveniles of 11 cold-temperate tree species , 2000, Oecologia.

[17]  P. Reich,et al.  Low-light carbon balance and shade tolerance in the seedlings of woody plants: Do winter deciduous and broad-leaved evergreen species differ? , 1999 .

[18]  D. Roff.  Phenotypic Evolution — A Reaction Norm Perspective , 1999, Heredity.

[19]  Andrew G. Peterson,et al.  Reconciling the apparent difference between mass- and area-based expressions of the photosynthesis-nitrogen relationship , 1999, Oecologia.

[20]  P. Reich,et al.  Evaluation of several measures of canopy openness as predictors of photosynthetic photon flux density in deeply shaded conifer-dominated forest understory , 1999 .

[21]  Hans Lambers,et al.  Plant Physiological Ecology , 2000, Springer New York.

[22]  D. L. Bell,et al.  Physiological response to complex environments in annual Polygonum species of contrasting ecological breadth , 1998, Oecologia.

[23]  P. Reich,et al.  Relationships of leaf dark respiration to leaf nitrogen, specific leaf area and leaf life-span: a test across biomes and functional groups , 1998, Oecologia.

[24]  Ph. Van.  GENERALISTS, SPECIALISTS, AND THE EVOLUTION OF PHENOTYPIC PLASTICITY IN SYMPATRIC POPULATIONS OF DISTINCT SPECIES. , 1997 .

[25]  P. H. Tienderen.  GENERALISTS, SPECIALISTS, AND THE EVOLUTION OF PHENOTYPIC PLASTICITY IN SYMPATRIC POPULATIONS OF DISTINCT SPECIES , 1997 .

[26]  W. G. Eickmeier,et al.  Comparative ecophysiology of a rare and a widespread species of Echinacea (Asteraceae) , 1994 .

[27]  J. M. Robinson.  Speculations on carbon dioxide starvation, Late Tertiary evolution of stomatal regulation and floristic modernization , 1994 .

[28]  R. Wetzel,et al.  Acclimation of photosynthetic phenotype to environmental heterogeneity , 1994 .

[29]  Paul G. Falkowski,et al.  Photoinhibition of Photosynthesis in Nature , 1994 .

[30]  John A. Silander,et al.  Sapling growth as a function of resources in a north temperate forest , 1994 .

[31]  S. Sultan,et al.  PHENOTYPIC PLASTICITY IN POLYGONUM PERSICARIA. III. THE EVOLUTION OF ECOLOGICAL BREADTH FOR NUTRIENT ENVIRONMENT , 1993, Evolution; international journal of organic evolution.

[32]  Harold A. Mooney,et al.  Responses of Plants to Multiple Stresses , 1993 .

[33]  Hendrik Poorter,et al.  Inherent Variation in Growth Rate Between Higher Plants: A Search for Physiological Causes and Ecological Consequences , 1992 .

[34]  F. Chapin.  3 – Effects of Multiple Environmental Stresses on Nutrient Availability and Use , 1991 .

[35]  Thomas J. Givnish,et al.  Adaptation to Sun and Shade: a Whole-Plant Perspective , 1988 .

[36]  D. Futuyma,et al.  The Evolution of Ecological Specialization , 1988 .

[37]  P. Nobel,et al.  STIPE ANATOMY, WATER POTENTIALS, AND XYLEM CONDUCTANCES IN SEVEN SPECIES OF FERNS (FILICOPSIDA) , 1982 .

[38]  O. Björkman.  Responses to Different Quantum Flux Densities , 1981 .

[39]  O. Lange.  Responses to the physical environment , 1981 .

[40]  C. Osmond,et al.  Physiological Plant Ecology I , 1981, Encyclopedia of Plant Physiology.

[41]  Robert K. Colwell,et al.  On the Measurement of Niche Breadth and Overlap. , 1971, Ecology.