Light foraging by trees is a fundamental process shaping forest communities. In heterogeneous light environments this behavior is expressed as plasticity of tree growth and the development of structural asymmetries. We studied the relative influence of neighborhood structure and directional solar ra

Plant architecture is crucial to pollination and mating in wind pollinated species. We investigate the effect of crown architecture on pollen dispersal, mating system and offspring quality, combining phenotypic and genotypic analyses in a low-density population of the endangered species Abies pinsap

Trait-based ecology predicts that evolution in high-resource agricultural environments should select for suites of traits that enable fast resource acquisition and rapid canopy closure. However, crop breeding targets specific agronomic attributes rather than broad trait syndromes. Breeding for speci

1) The concentration, stoichiometry, and resorption of nitrogen (N) and phosphorus (P) in plant leaves are often used as proxies of the availability of these growth-limiting nutrients, but the responses of these metrics to changes in nutrient availability remains largely untested for tropical forest

1. Despite extensive development of successional theory, few empirical studies have evaluated whether existing models are applicable to human-modified landscapes. Seasonally dry tropical forests are experiencing widespread transformation, and represent a critical system to assess in a successional f

Genomic selection (GS) is of interest in breeding because of its potential for predicting the genetic value of individuals and increasing genetic gains per unit of time. To date, very few studies have reported empirical results of GS potential in the context of large population sizes and long breedi

Interspecific hybridization may enhance the capacity of populations to adapt to changing environments, and has practical implications for reforestation. We use genomewide estimates of admixture and phenotypic traits for trees in a common garden to examine the extent and direction of gene flow across

Assessing the potential for forest carbon (C) capture and storage requires accurate assessments of C in live tree tissues. In the vast majority of local, regional, and global assessments, C content has been assumed to be 50% of tree biomass; however, recent studies indicate that this assumption is n

Intraspecific adaptation in Abies sachalinensis was examined using models based on long-term monitoring data gathered during a reciprocal transplant experiment with eight seed source populations and six transplantation sites along an altitudinal gradient. The consequence of local adaptation was eval

Tree ring data from the International Tree Ring Data Bank and World Data Center for Paleoclimatology archives. Most data sets include raw treering measurements (most are annual ring width, with some collections of earlywood or latewood width or wood density), plus chronologies (standardized growth i

Tree ring data from the International Tree Ring Data Bank and World Data Center for Paleoclimatology archives. Most data sets include raw treering measurements (most are annual ring width, with some collections of earlywood or latewood width or wood density), plus chronologies (standardized growth i

The Southern Rockies LCC is home to narrowleaf cottonwood (Populus angustifolia), common at elevations above 1800 m, and Fremont cottonwood [a common name regionally attached to the ecologically very similar Populus fremontii subsp. fremontii S. Watson and P. deltoides subsp. wislizenii (S. Watson)

The Southern Rockies LCC is home to narrowleaf cottonwood (Populus angustifolia), common at elevations above 1800 m, and Fremont cottonwood [a common name regionally attached to the ecologically very similar Populus fremontii subsp. fremontii S. Watson and P. deltoides subsp. wislizenii (S. Watson)

The Southern Rockies LCC is home to narrowleaf cottonwood (Populus angustifolia), common at elevations above 1800 m, and Fremont cottonwood [a common name regionally attached to the ecologically very similar Populus fremontii subsp. fremontii S. Watson and P. deltoides subsp. wislizenii (S. Watson)

The Southern Rockies LCC is home to narrowleaf cottonwood (Populus angustifolia), common at elevations above 1800 m, and Fremont cottonwood [a common name regionally attached to the ecologically very similar Populus fremontii subsp. fremontii S. Watson and P. deltoides subsp. wislizenii (S. Watson)

The Southern Rockies LCC is home to narrowleaf cottonwood (Populus angustifolia), common at elevations above 1800 m, and Fremont cottonwood [a common name regionally attached to the ecologically very similar Populus fremontii subsp. fremontii S. Watson and P. deltoides subsp. wislizenii (S. Watson)

The Southern Rockies LCC is home to narrowleaf cottonwood (Populus angustifolia), common at elevations above 1800 m, and Fremont cottonwood [a common name regionally attached to the ecologically very similar Populus fremontii subsp. fremontii S. Watson and P. deltoides subsp. wislizenii (S. Watson)

The Southern Rockies LCC is home to narrowleaf cottonwood (Populus angustifolia), common at elevations above 1800 m, and Fremont cottonwood [a common name regionally attached to the ecologically very similar Populus fremontii subsp. fremontii S. Watson and P. deltoides subsp. wislizenii (S. Watson)

The Southern Rockies LCC is home to narrowleaf cottonwood (Populus angustifolia), common at elevations above 1800 m, and Fremont cottonwood [a common name regionally attached to the ecologically very similar Populus fremontii subsp. fremontii S. Watson and P. deltoides subsp. wislizenii (S. Watson)

The Southern Rockies LCC is home to narrowleaf cottonwood (Populus angustifolia), common at elevations above 1800 m, and Fremont cottonwood [a common name regionally attached to the ecologically very similar Populus fremontii subsp. fremontii S. Watson and P. deltoides subsp. wislizenii (S. Watson)