The effective number of species ( We used simulations of five stream macroinvertebrate assemblages and spatially extensive field data of stream fishes and mussels to show (a) how different Values of The amount of variation in
Generalization is difficult to quantify, and many classifications exist. A beta diversity framework can be used to establish a numeric measure of generalist tendencies that jointly describes many important features of species interactions, namely spatiotemporal heterogeneity. This framework is promising for studying generalized symbiotic relationships of any form. We formulated a novel index, turnover importance ( Alternative interactor‐specific measures of generalism are best employed for local‐level community networks over short timespans. While these interactor metrics can assess use versus availability in local communities,
- NSF-PAR ID:
- 10500336
- Publisher / Repository:
- Wiley-Blackwell
- Date Published:
- Journal Name:
- Methods in Ecology and Evolution
- Volume:
- 15
- Issue:
- 5
- ISSN:
- 2041-210X
- Format(s):
- Medium: X Size: p. 951-964
- Size(s):
- p. 951-964
- Sponsoring Org:
- National Science Foundation
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Weighting effective number of species measures by abundance weakens detection of diversity responses
Abstract ENS ) has been proposed as a robust measure of species diversity that overcomes several limitations in terms of both diversity indices and species richness (SR). However, it is not yet clear ifENS improves interpretation and comparison of biodiversity monitoring data, and ultimately resource management decisions.ENS formulations respond to stress and (b) how diversity–environment relationships change with values ofq , which weightENS measures by species abundances.ENS derived from whole simulated assemblages with all species weighted equally (true SR) steadily decreased as stress increased, andENS ‐stress relationships became weaker and more different among assemblages with increased weighting.ENS across the fish and mussel assemblages that was associated with environmental gradients decreased with increasingq .Synthesis and applications . Species diversity is valued by many human societies, which often have policies designed to protect and restore it. Natural resources managers and policy makers may use species richness and diversity indices to describe the status of ecological communities. However, these traditional diversity measures are known subject to limitations that hinder their interpretation and comparability. The effective number of species (ENS ) was proposed to overcome the limitations. Unfortunately, our analyses show thatENS does not improve interpretability of how species diversity responds to either stress or natural environmental gradients. Moreover, incorporating the relative abundance of individuals in different species (evenness) into diversity measures as implemented inENS can actually weaken detection of diversity responses. Natural resources managers and policy makers therefore need to be cautious when interpreting diversity measures, includingENS , whose values are jointly influenced by richness and evenness. We suggest that both researchers and practitioners measure and report three aspects of diversity (species richness, evenness, and composition) separately when assessing and monitoring the diversity of ecological communities. -
Abstract The field of eco‐evolutionary dynamics is developing rapidly, with a growing number of well‐designed experiments quantifying the impact of evolution on ecological processes and patterns, ranging from population demography to community composition and ecosystem functioning. The key challenge remains to transfer the insights of these proof‐of‐principle experiments to natural settings, where multiple species interact and the dynamics are far more complex than those studied in most experiments.
Here, we discuss potential pitfalls of building a framework on eco‐evolutionary dynamics that is based on data on single species studied in isolation from interspecific interactions, which can lead to both under‐ and overestimation of the impact of evolution on ecological processes. Underestimation of evolution‐driven ecological changes could occur in a single‐species approach when the focal species is involved in co‐evolutionary dynamics, whereas overestimation might occur due to increased rates of evolution following ecological release of the focal species.
In order to develop a multi‐species perspective on eco‐evolutionary dynamics, we discuss the need for a broad‐sense definition of “eco‐evolutionary feedbacks” that includes any reciprocal interaction between ecological and evolutionary processes, next to a narrow‐sense definition that refers to interactions that directly feed back on the interactor that evolves.
We discuss the challenges and opportunities of using more natural settings in eco‐evolutionary studies by gradually adding complexity: (a) multiple interacting species within a guild, (b) food web interactions and (c) evolving metacommunities in multiple habitat patches in a landscape. A literature survey indicated that only a few studies on microbial systems so far developed a truly multi‐species approach in their analysis of eco‐evolutionary dynamics, and mostly so in artificially constructed communities.
Finally, we provide a road map of methods to study eco‐evolutionary dynamics in more natural settings. Eco‐evolutionary studies involving multiple species are necessarily demanding and might require intensive collaboration among research teams, but are highly needed.
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Abstract The prediction that higher biodiversity leads to denser niche packing and thus higher community resistance to invasion has long been studied, with species richness as the predominant measure of diversity. However, few studies have explored how phylogenetic and functional diversity, which should represent niche space more faithfully than taxonomic diversity, influence community invasibility, especially across longer time frames and over larger spatial extents.
We used a 15‐year, 150‐site grassland dataset to assess relationships between invasive plant abundance and phylogenetic, functional and taxonomic diversity of recipient native plant communities. We analysed the dataset both pooled across all surveys and longitudinally, leveraging time‐series data to compare observed patterns in invasion with those predicted by two community assembly processes: biotic resistance and competitive exclusion. We expected more phylogenetically and functionally diverse communities to exhibit greater resistance to invasion.
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Abstract Assemblages of insect herbivores are structured by plant traits such as nutrient content, secondary metabolites, physical traits, and phenology. Many of these traits are phylogenetically conserved, implying a decrease in trait similarity with increasing phylogenetic distance of the host plant taxa. Thus, a metric of phylogenetic distances and relationships can be considered a proxy for phylogenetically conserved plant traits and used to predict variation in herbivorous insect assemblages among co‐occurring plant species.
Using a Holarctic dataset of exposed‐feeding and shelter‐building caterpillars, we aimed at showing how phylogenetic relationships among host plants explain compositional changes and characteristics of herbivore assemblages.
Our plant–caterpillar network data derived from plot‐based samplings at three different continents included >28,000 individual caterpillar–plant interactions. We tested whether increasing phylogenetic distance of the host plants leads to a decrease in caterpillar assemblage overlap. We further investigated to what degree phylogenetic isolation of a host tree species within the local community explains abundance, density, richness, and mean specialization of its associated caterpillar assemblage.
The overlap of caterpillar assemblages decreased with increasing phylogenetic distance among the host tree species. Phylogenetic isolation of a host plant within the local plant community was correlated with lower richness and mean specialization of the associated caterpillar assemblages. Phylogenetic isolation had no effect on caterpillar abundance or density. The effects of plant phylogeny were consistent across exposed‐feeding and shelter‐building caterpillars.
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