This file contains data from the experiment at Carpenter Meadow to assess natural selection on flowering in local genotypes. Jill Anderson collected data in the field in 2010. Analyses included size at planting (number of leaves) and cohort as fixed effects, and row nested within block as random eff

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

Gene flow from transgenic crops allows novel traits to spread to sexually compatible weeds. Traits such as resistance to insects may enhance the fitness of weeds, but few studies have tested for these effects under natural field conditions. We created F2 and F3 crop-weed hybrid lineages of genetical

Specialization is common in most lineages of insect herbivores, one of the most diverse groups of organisms on earth. To address how and why specialization is maintained over evolutionary time, we hypothesized that plant defense and other ecological attributes of potential host plants would predict

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

Multiple unlinked genetic loci often provide a more comprehensive picture of evolutionary history than any single gene can, but analyzing multigene data presents particular challenges. Differing rates and patterns of nucleotide substitution, combined with the limited information available in any dat

We conducted a phylogenetic study of pygopodid lizards, a group of 38 species endemic to Australia and New Guinea, with two major goals:to reconstruct a taxonomically complete and robustly supported phylogeny for the group and to use this information to gain insights into the tempo, mode, and timing

This table contains 37 years of demographic data for 12 sites. The trap record for each animal for each year the animal was present includes age, sex, locality, and reproductive status. Also included, when known, are changes in location, fate (predation death, dispersed), and genetic information (al

This table contains 37 years of demographic data for 12 sites. The trap record for each animal for each year the animal was present includes age, sex, locality, and reproductive status. Also included, when known, are changes in location, fate (predation death, dispersed), and genetic information (al

This table contains 37 years of demographic data for 12 sites. The trap record for each animal for each year the animal was present includes age, sex, locality, and reproductive status. Also included, when known, are changes in location, fate (predation death, dispersed), and genetic information (al

This table contains 37 years of demographic data for 12 sites. The trap record for each animal for each year the animal was present includes age, sex, locality, and reproductive status. Also included, when known, are changes in location, fate (predation death, dispersed), and genetic information (al

This table contains 37 years of demographic data for 12 sites. The trap record for each animal for each year the animal was present includes age, sex, locality, and reproductive status. Also included, when known, are changes in location, fate (predation death, dispersed), and genetic information (al

This table contains 37 years of demographic data for 12 sites. The trap record for each animal for each year the animal was present includes age, sex, locality, and reproductive status. Also included, when known, are changes in location, fate (predation death, dispersed), and genetic information (al

This table contains 37 years of demographic data for 12 sites. The trap record for each animal for each year the animal was present includes age, sex, locality, and reproductive status. Also included, when known, are changes in location, fate (predation death, dispersed), and genetic information (al

This table contains 37 years of demographic data for 12 sites. The trap record for each animal for each year the animal was present includes age, sex, locality, and reproductive status. Also included, when known, are changes in location, fate (predation death, dispersed), and genetic information (al

This table contains 37 years of demographic data for 12 sites. The trap record for each animal for each year the animal was present includes age, sex, locality, and reproductive status. Also included, when known, are changes in location, fate (predation death, dispersed), and genetic information (al

This table contains 37 years of demographic data for 12 sites. The trap record for each animal for each year the animal was present includes age, sex, locality, and reproductive status. Also included, when known, are changes in location, fate (predation death, dispersed), and genetic information (al

This table contains 36 years of demographic data for 12 sites. The trap record for each animal for each year the animal was present includes age, sex, locality, and reproductive status. Also included, when known, are changes in location, fate (predation death, dispersed), and genetic information (al

This table contains 36 years of demographic data for 12 sites. The trap record for each animal for each year the animal was present includes age, sex, locality, and reproductive status. Also included, when known, are changes in location, fate (predation death, dispersed), and genetic information (al

This table contains 36 years of demographic data for 12 sites. The trap record for each animal for each year the animal was present includes age, sex, locality, and reproductive status. Also included, when known, are changes in location, fate (predation death, dispersed), and genetic information (al