Size-dependent changes in light requirements of tropical trees: weak light-growth relationships in seven Caribbean rainforest species preclude testing a general hypothesis

In tropical forests light is presumed to be the most important limiting resource for trees below the forest canopy, and interspecific variation in shade tolerance an important driver of tree community composition. It has been hypothesized that tree light requirements may increase with tree size, but to date no study has explicitly quantified ontogenetic changes in light requirements for tropical trees. Here we make use of a field measure of whole-plant light compensation point (WPLCP) to quantify size-related shifts in light requirements of seven Dominican rainforest tree species, at two distinct size categories: saplings and pole-size juveniles. Although our dataset was large (representing 429 trees remeasured over a 13-month period), relative tree growth rate was only weakly related to estimated light levels ( r 2 = 0–0.36) across all species/size groups, and WPLCP could thus only be estimated for saplings of three species, and juveniles of one species. Both sapling and juvenile WPLCPs were significant for only one species, where we observed a size-dependent decrease in light requirements, a result contradicting our hypothesis. However, generalizations possible from our dataset are limited, as WPLCP could not be accurately determined within species/size groups, and did not match a priori qualitative shade-tolerance rankings. Overall, our data neither confirm nor deny a hypothesized ontogenetic increase in light requirements of tropical trees. We suggest that the highly dynamic canopies of Dominican rainforests due to strong, persistent winds on the island make estimates of understory light levels using hemispherical photography unreliable: a limitation that is likely present, though less pronounced, in many forest ecosystems.

[1]  Nathan J B Kraft,et al.  Functional traits and the growth-mortality trade-off in tropical trees. , 2010, Ecology.

[2]  C. Canham,et al.  Shade tolerance, canopy gaps and mechanisms of coexistence of forest trees , 2010 .

[3]  C. Collier,et al.  The land below the wind: Doppler LiDAR observations from the tropical rain forest of Sabah, Borneo, Malaysia , 2010 .

[4]  D. Coomes,et al.  Size‐dependence of growth and mortality influence the shade tolerance of trees in a lowland temperate rain forest , 2009 .

[5]  S. Hubbell,et al.  Local neighborhood and species' shade tolerance influence survival in a diverse seedling bank. , 2009, Ecology.

[6]  Ü. Niinemets,et al.  Shade Tolerance, a Key Plant Feature of Complex Nature and Consequences , 2008 .

[7]  D. Falster,et al.  Ontogenetic variation in light requirements of juvenile rainforest evergreens , 2008 .

[8]  Phillip B. Schafer,et al.  Orographic Precipitation in the Tropics: Experiments in Dominica , 2008 .

[9]  J. Baltzer,et al.  Determinants of whole‐plant light requirements in Bornean rain forest tree saplings , 2007 .

[10]  J. Baltzer,et al.  Physiological and morphological correlates of whole-plant light compensation point in temperate deciduous tree seedlings , 2007, Oecologia.

[11]  L. Poorter,et al.  Carbohydrate storage and light requirements of tropical moist and dry forest tree species. , 2007, Ecology.

[12]  Ü. Niinemets The controversy over traits conferring shade‐tolerance in trees: ontogenetic changes revisited , 2006 .

[13]  Jing M. Chen,et al.  Determining digital hemispherical photograph exposure for leaf area index estimation , 2005 .

[14]  J. Makana,et al.  Effects of Light Gaps and Litter Removal on the Seedling Performance of Six African Timber Species 1 , 2005 .

[15]  F. Bongers,et al.  Beyond the regeneration phase: differentiation of height–light trajectories among tropical tree species , 2005 .

[16]  C. Messier,et al.  Interacting influence of light and size on aboveground biomass distribution in sub-boreal conifer saplings with contrasting shade tolerance. , 2005, Tree Physiology.

[17]  Michael Nobis,et al.  Automatic thresholding for hemispherical canopy-photographs based on edge detection , 2005 .

[18]  C. Messier,et al.  Light and tree size influence belowground development in yellow birch and sugar maple , 2005, Plant and Soil.

[19]  Mike S. Fowler,et al.  Editorial: The Journal of Negative Results in Ecology and Evolutionary Biology , 2004 .

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

[21]  T. Nakashizuka,et al.  Allocation to defense or growth in dipterocarp forest seedlings in Borneo , 2004, Oecologia.

[22]  C. Messier,et al.  Physiological, morphological and allocational plasticity in understory deciduous trees: importance of plant size and light availability. , 2004, Tree physiology.

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

[24]  M. Turnbull The effect of light quantity and quality during development on the photosynthetic characteristics of six Australian rainforest tree species , 1991, Oecologia.

[25]  M. Swaine,et al.  On the definition of ecological species groups in tropical rain forests , 1988, Vegetatio.

[26]  Michael D. Jennions,et al.  Meta‐analysis can “fail”: reply to Kotiaho and Tomkins , 2004 .

[27]  C. Augspurger,et al.  Differences in leaf phenology between juvenile and adult trees in a temperate deciduous forest. , 2003, Tree physiology.

[28]  A. Leakey,et al.  Patterns of dynamic irradiance affect the photosynthetic capacity and growth of dipterocarp tree seedlings , 2003, Oecologia.

[29]  Hong S. He,et al.  A simulation study of landscape scale forest succession in northeastern China , 2002 .

[30]  Mark R. Fulton,et al.  Sapling growth and survivorship as a function of light in a mesic forest of southeast Texas, USA , 2002, Oecologia.

[31]  L. Alados-Arboledas,et al.  Improved estimation of diffuse photosynthetically active radiation using two spectral models , 2002 .

[32]  C. Messier,et al.  Growth and crown morphological responses of boreal conifer seedlings and saplings with contrasting shade tolerance to a gradient of light and height , 2002 .

[33]  W. Winner,et al.  Photosynthetic differences between saplings and adult trees: an integration of field results by meta-analysis. , 2002, Tree physiology.

[34]  K. Cao Morphology and growth of deciduous and evergreen broad-leaved saplings under different light conditions in a Chinese beech forest with dense bamboo undergrowth , 2001, Ecological Research.

[35]  D. Bates,et al.  Mixed-Effects Models in S and S-PLUS , 2001 .

[36]  L. Poorter Light-dependent changes in biomass allocation and their importance for growth of rain forest tree species , 2001 .

[37]  P. Reich,et al.  SEED SIZE, NITROGEN SUPPLY, AND GROWTH RATE AFFECT TREE SEEDLING SURVIVAL IN DEEP SHADE , 2000 .

[38]  P. Reich,et al.  Trade‐offs in low‐light CO2 exchange: a component of variation in shade tolerance among cold temperate tree seedlings , 2000 .

[39]  Frans Bongers,et al.  The effect of tree height and light availability on photosynthetic leaf traits of four neotropical species differing in shade tolerance , 2000 .

[40]  Seiwa Ontogenetic changes in leaf phenology of Ulmus davidiana var. japonica, a deciduous broad-leaved tree. , 1999, Tree physiology.

[41]  Lourens Poorter,et al.  Growth responses of 15 rain‐forest tree species to a light gradient: the relative importance of morphological and physiological traits , 1999 .

[42]  C. Messier,et al.  Functional ecology of advance regeneration in relation to light in boreal forests , 1999 .

[43]  K. Seiwa,et al.  Changes in Leaf Phenology are Dependent on Tree Height inAcer mono, a Deciduous Broad-leaved Tree , 1999 .

[44]  R. Kobe LIGHT GRADIENT PARTITIONING AMONG TROPICAL TREE SPECIES THROUGH DIFFERENTIAL SEEDLING MORTALITY AND GROWTH , 1999 .

[45]  R. Kobe Carbohydrate allocation to storage as a basis of interspecific variation in sapling survivorship and growth , 1997 .

[46]  S. Pacala,et al.  Forest models defined by field measurements : Estimation, error analysis and dynamics , 1996 .

[47]  John A. Silander,et al.  Juvenile Tree Survivorship as a Component of Shade Tolerance , 1995 .

[48]  David B. Clark,et al.  LIFE HISTORY DIVERSITY OF CANOPY AND EMERGENT TREES IN A NEOTROPICAL RAIN FOREST , 1992 .

[49]  S. Hubbell,et al.  Short-term dynamics of a neotropical forest: why ecological research matters to tropical conservation and management , 1992 .

[50]  A. Moad Dipterocarp juvenile growth and understory light availability in Malaysian tropical forest , 1992 .

[51]  R. Chazdon,et al.  The Importance of Sunflecks for Forest Understory Plants Photosynthetic machinery appears adapted to brief, unpredictable periods of radiation , 1991 .

[52]  A. Lack Dead logs as a substrate for rain forest trees in Dominica , 1991, Journal of Tropical Ecology.

[53]  D. Nicolson,et al.  Flora of Dominica, Part 2: Dicotyledoneae , 1991 .

[54]  D. A. King Correlations between biomass allocation, relative growth rate and light environment in tropical forest saplings , 1991 .

[55]  T. Kohyama A functional model describing sapling growth under a tropical forest canopy , 1991 .

[56]  Robert W. Pearcy,et al.  SUNFLECKS AND PHOTOSYNTHESIS IN PLANT CANOPIES , 1990 .

[57]  F. Stuart Chapin,et al.  The Ecology and Economics of Storage in Plants , 1990 .

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

[59]  Richard H. Waring,et al.  Characteristics of Trees Predisposed to Die , 1987 .

[60]  P. Grubb THE MAINTENANCE OF SPECIES‐RICHNESS IN PLANT COMMUNITIES: THE IMPORTANCE OF THE REGENERATION NICHE , 1977 .

[61]  J. Connell On the role of the natural enemies in preventing competitive exclusion in some marine animals and in rain forest trees , 1971 .

[62]  D. Janzen Herbivores and the Number of Tree Species in Tropical Forests , 1970, The American Naturalist.

[63]  F. S. Baker A Revised Tolerance Table , 1949 .

[64]  W. Hodge The Vegetation of Dominica , 1943 .