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Kriebel, R.

Publications and source records attributed to Kriebel, R..

3 recordsLinked to original sources

Buzz-world: Global patterns and drivers of buzzing bees and poricidal plants

Foraging behavior frequently plays a major role in driving the geographic distribution of animals. Buzzing to extract protein-rich pollen from flowers is a key foraging behavior used by bee species across at least 83 genera (these genera comprise [~]58% of all bee species). Although buzzing is widely recognized to affect the ecology and evolution of bees and flowering plants (e.g., buzz-pollinated flowers), global patterns and drivers of buzzing bee biogeography remain unexplored. Here, we investigate the global species distribution patterns within each bee family and how patterns and drivers differ with respect to buzzing bee species. We found that both distributional patterns and drivers of richness typically differed for buzzing species compared to hotspots for all bee species and when grouped by family. A major predictor of the distribution, but not species richness overall for buzzing members of four of the five major bee families included in analyses (Andrenidae, Halictidae, Colletidae and to a lesser extent, Apidae) was the richness of poricidal flowering plant species, which depend on buzzing bees for pollination. As poricidal plant richness was highest in areas with low wind and high aridity, we discuss how global hotspots of buzzing bee biodiversity are likely driven by both biogeographic factors and plant host availability. Whilst we explored global patterns with State-level data, higher resolution work is needed to explore local level drivers of patterns, but from a global perspective, buzz-pollinated plants clearly play a greater role in the ecology and evolution of buzzing bees than previously predicted.

ecology↗

Widespread evolution of poricidal flowers: A striking example of morphological convergence across flowering plants

The evolution of tube-like floral morphologies that control pollen release via small openings (functionally poricidal flowers) represents a taxonomically and geographically widespread instance of repeated and independent evolution of a functionally similar morphology. Poricidal flowers are also often closely associated with buzz pollination by bees. Yet we lack an updated angiosperm-wide survey of their phylogenetic distribution. We identify all known angiosperm genera containing poricidal flowers via a literature survey. We determined their phylogenetic distribution and minimum number of independent gains and losses via a species-level angiosperm-wide phylogeny. We estimated if evolution of poricidal flowers is associated with changes in speciation/extinction via diversification rate analyses. Poricidal flowers occur across 87 angiosperm families and 639 genera containing >28,000 species. At the species level, an average of 205 independent gains and 215 losses of poricidal flowers occurred. Angiosperm-wide analyses suggest an early burst in poricidal evolution, but no differences in net diversification (origination-extinction) between non-poricidal and poricidal taxa. Analyses for two focal families however indicate strong context-dependent effects of poricidal flowers on diversification. Poricidal evolution thus represents a large-scale example of convergent evolution in floral form, but effects on diversification appear to be strongly contingent on phylogenetic and ecological background.

evolutionary biology↗

Phylogenetic Comparative Methods on Phylogenetic Networks with Reticulations

The goal of Phylogenetic Comparative Methods (PCMs) is to study the distribution of quantitative traits among related species. The observed traits are often seen as the result of a Brownian Motion (BM) along the branches of a phylogenetic tree. Reticulation events such as hybridization, gene flow or horizontal gene transfer, can substantially affect a species traits, but are not modeled by a tree. Phylogenetic networks have been designed to represent reticulate evolution. As they become available for downstream analyses, new models of trait evolution are needed, applicable to networks. One natural extension of the BM is to use a weighted average model for the trait of a hybrid, at a reticulation point. We develop here an efficient recursive algorithm to compute the phylogenetic variance matrix of a trait on a network, in only one preorder traversal of the network. We then extend the standard PCM tools to this new framework, including phylogenetic regression with covariates (or phylogenetic ANOVA), ancestral trait reconstruction, and Pagels {lambda} test of phylogenetic signal. The trait of a hybrid is sometimes outside of the range of its two parents, for instance because of hybrid vigor or hybrid depression. These two phenomena are rather commonly observed in present-day hybrids. Transgressive evolution can be modeled as a shift in the trait value following a reticulation point. We develop a general framework to handle such shifts, and take advantage of the phylogenetic regression view of the problem to design statistical tests for ancestral transgressive evolution in the evolutionary history of a group of species. We study the power of these tests in several scenarios, and show that recent events have indeed the strongest impact on the trait distribution of present-day taxa. We apply those methods to a dataset of Xiphophorus fishes, to confirm and complete previous analysis in this group. All the methods developed here are available in the Julia package PhyloNetworks.

evolutionary biology↗