Abstract

Measuring species-specific competitive interactions is key to understanding plant communities. Repeat censused large forest dynamics plots offer an ideal setting to measure these interactions by estimating the species-specific competitive effect on neighboring tree growth. Estimating these interaction values can be difficult, however, because the number of them grows with the square of the number of species. Furthermore, confidence in the estimates can be overestimated if any spatial structure of model errors is not considered. Here we measured these interactions in a forest dynamics plot in a transitional oak-hickory forest. We analytically fit Bayesian linear regression models of annual tree radial growth as a function of that tree's species, its size, and its neighboring trees. We then compared these models to test whether the identity of a tree's neighbors matters and if so at what level: based on trait grouping, based on phylogenetic family, or based on species. We used a spatial cross-validation scheme to better estimate model errors while avoiding potentially over-fitting our models. Since our model is analytically solvable we can rapidly evaluate it, which allows our proposed cross-validation scheme to be computationally feasible. We found that the identity of the focal and competitor trees mattered for competitive interactions, but surprisingly, identity mattered at the family rather than species-level.

Highlights

  • Competition is a key biotic interaction which structures communities

  • Attempts have been made to do this through direct measurement of species-specific competition coefficients, or to generalize competitive interactions based on trait or phylogeny differences between competitors

  • For all three groupings the identity of the competitor did matter; the root mean-squared error (RMSE) with actual competitor identity was less than the RSME when the competitor identity was permuted (Fig 2 compare the dotted horizontal lines to the histograms)

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Summary

Introduction

Competition is a key biotic interaction which structures communities. To better understand the role it plays, we need ways to understand species-specific competitive interactions. Attempts have been made to do this through direct measurement of species-specific competition coefficients, or to generalize competitive interactions based on trait or phylogeny differences between competitors. Repeat censused forest inventory plots are good places to measure species-specific competition. In such forests trees are identified, mapped, and have their diameter measured at regular time intervals [1, 2].

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