Plant Diversity and Diversification
Plants have successfully colonized almost all of the Earth ecosystems and are among the most diverse eukaryote phyla (Mora et al., 2011; Pimm and Joppa, 2015). They also play a key role in the Earth system as a major actor in atmospheric, water and nutrient cycles that make possible life as we know it (Lucas, 2001; Payne et al., 2020). Numerous studies focused on plant diversity and evolution have been published and a large body of knowledge on plant diversity, evolutionary history, traits, physiology, and distribution has been generated. Such accumulation of knowledge combined with methodological and computational advances, and the ever-expanding biological databases (e.g., GenBank, TRY, GBIF) have allowed the study of plant diversity at large geographical and temporal scales as exemplified on Figure 1 (Zanne et al., 2014; Smith and Brown, 2018; Igea and Tanentzap, 2020; Neves et al., 2021). However, despite numerous advances, plant diversity and diversification patterns remain contentions. For example, there is still no consensus about the crown age of angiosperms (flowering plants, the most diverse plant lineage) (e.g., Barba-Montoya et al., 2018; Sauquet et al., 2021). Many species remain undescribed and a large fraction of the described species have never been included in phylogenetic datasets (Stevens, 2017). Likewise, large gaps remain in distributional and trait databases (Cornwell et al., 2019).
Figure 1
The aim of this Research Topic is to bring together research that furthers our understanding of large-scale plant diversity and diversification patterns. It includes nine papers that tackle these issues from different evolutionary and ecological perspectives using diverse methods and study systems.
Evolutionary and Ecological Drivers of Plant Diversity Patterns
Most of the articles in this Research Topic focus on the drivers of plant diversity and distribution patterns. Loiseau et al., using genome skimming data of the hyperdiverse genus Vriesea (Bromeliaceae), show that hybridization have likely played a major role in the diversification of this genus. Their results provide further evidence for the potential importance of hybridization for the diversification of Bromeliaceae.
Dispersal abilities and phenotypic adaptations are essential for the success of taxa in changing environments. Bitencourt et al. study the evolution of dispersal, habit, and pollination in Apocynaceae. They find that evolution of wind-dispersed seeds, climbing growth form, and pollinia have jointly shaped the diversification and diversity patterns of this family across Africa.
Fernandes et al. take a different approach and study the processes that have shaped the flora in a geographical region. They show that most lineages restricted to the Brazilian Caatinga seasonally dry forest emerged only recently during the Miocene when the region became drier. They also discuss the importance of local diversification processes driven by regional-scale geological history and local adaptations.
Diversity patterns along elevational gradients have attracted biologists since the time of Humboldt and Bonpland (1805). Griffiths et al. use plot inventory data and published phylogenies to investigate how evolutionary diversity varies along an elevation gradient. Similarly to taxonomic diversity (Rahbek, 1995), they find a mid-elevation pick in evolutionary diversity and they interpret this as a support for the Environmental Crossroads Hypothesis (Neves et al., 2020).
Song et al. study the patterns of species richness of bryophytes in China and find that the tropical and subtropical montane regions in China are both centers of diversification and refugia for bryophyte species. Different functional traits allow plant species to establish in diverse environments and co-exists in complex communities.
Yang et al. contribution investigates the patterns of leaf traits relationships in the Tibetan plateau, and the importance of particular traits for the adaptation of plants to aquatic environments.
Sedio et al. study chemical similarity among co-occurring trees and based on the comparison of more than 13,000 leaf metabolites conclude that plant metabolomes play an important role in community assembly. However, their importance is not homogenous along environmental gradients and is higher in wetter and warmer climates.
Defining Biomes and Predicting Future Distributions
Defining biomes and predicting suitable areas for species are central for conservation planning in the context of ongoing global warming.
Cardoso et al. present a new approach to biome delimitation that incorporates floristic, functional, and phylogenetic data and environmentally trained species distribution models. Their comprehensive analyses support a new, biologically meaningful delimitation of terrestrial biomes in eastern Brazil.
Global warming may cause major changes in the areas suitable for the growth and cultivation of plant species. Yan et al. estimate the areas that would be potentially suitable for Codonopsis pilosula (a medicinal plant from China) under global warming and suggest which regions may be optimal to cultivate this species.
Concluding Remarks
The articles in this Research Topic shed light on different aspects of plant diversity and diversification patterns in different regions of the world, across environmental gradients or trough evolutionary time. This Research Topic has highlighted the potential of integrative approaches that combine evolutionary, ecological, environmental, and geological data. It has also opened new questions and has provided new tools for future studies, and we hope that readers will find inspiration in the research presented here.
Funding
DMN acknowledges support from the US NSF (DEB-1556651) and Instituto Serrapilheira/Brazil (Serra-1912-32082). XX acknowledges support from the National Science Foundation of China (31770566).
Publisher's Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Statements
Author contributions
DD, DMN and XX wrote the article together and all authors approved the submitted version.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
References
1
Barba-MontoyaJ.ReisM.dos SchneiderH.DonoghueP. C. J.YangZ. (2018). Constraining uncertainty in the timescale of angiosperm evolution and the veracity of a Cretaceous Terrestrial Revolution. New Phytol.218, 819–834. 10.1111/nph.15011
2
CornwellW. K.PearseW. D.DalrympleR. L.ZanneA. E. (2019). What we (don't) know about global plant diversity. Ecography42, 1819–1831. 10.1111/ecog.04481
3
HumboldtA.BonplandA. (1805). Essai sur la géographie des plantes. Paris: Schoell et Cie.
4
IgeaJ.TanentzapA. J. (2020). Angiosperm speciation cools down in the tropics. Ecol. Lett.23, 692–700. 10.1111/ele.13476
5
LucasY. (2001). The role of plants in controlling rates and products of weathering: importance of biological pumping. Annu. Rev. Earth Planet. Sci.29, 135–163. 10.1146/annurev.earth.29.1.135
6
MaitnerB. S.BoyleB.CaslerN.ConditR.DonoghueI. I. J.et al. (2018). The bien r package: a tool to access the Botanical Information and Ecology Network (BIEN) database. Methods Ecol. Evol.9, 373–379. 10.1111/2041-210X.12861
7
MoraC.TittensorD. P.AdlS.SimpsonA. G. B.WormB. (2011). How many species are there on earth and in the ocean?PLOS Biol.9, e1001127. 10.1371/journal.pbio.1001127
8
NevesD. M.DexterK. G.BakerT. R.Coelho de SouzaF.Oliveira-FilhoA. T.QueirozL. P.et al. (2020). Evolutionary diversity in tropical tree communities peaks at intermediate precipitation. Sci. Rep.10, 1188. 10.1038/s41598-019-55621-w
9
NevesD. M.KerkhoffA. J.Echeverría-LondoñoS.MerowC.Morueta-HolmeN.PeetR. K.et al. (2021). The adaptive challenge of extreme conditions shapes evolutionary diversity of plant assemblages at continental scales. Proc. Natl. Acad. Sci.118, e2021132118. 10.1073/pnas.2021132118
10
PayneJ. L.BachanA.HeimN. A.HullP. M.KnopeM. L. (2020). The evolution of complex life and the stabilization of the Earth system. Interface Focus10, 20190106. 10.1098/rsfs.2019.0106
11
PimmS. L.JoppaL. N. (2015). How many plant species are there, where are they, and at what rate are they going extinct?Ann. Mol. Bot. Gard.100, 170–176. 10.3417/2012018
12
RahbekC. (1995). The elevational gradient of species richness: a uniform pattern?Ecography18, 200–205
13
SauquetH.Ramírez-BarahonaS.MagallónS. (2021). The age of flowering plants is unknown. EcoEvoRxiv.10.32942/osf.io/n4v6b
14
SmithS. A.BrownJ. W. (2018). Constructing a broadly inclusive seed plant phylogeny. Am. J. Bot.105, 302–314. 10.1002/ajb2.1019
15
StevensP. F. (2017). Angiosperm Phylogeny Website. Version 14. Available online at: http://www.mobot.org/MOBOT/research/APweb/ (accessed November 13, 2015).
16
ZanneA. E.TankD. C.CornwellW. K.EastmanJ. M.SmithS. A.FitzJohnR. G.et al. (2014). Three keys to the radiation of angiosperms into freezing environments. Nature506, 89–92. 10.1038/nature12872
Summary
Keywords
species richness, environmental gradients, traits, macroecology, macroevolution
Citation
Dimitrov D, Neves DM and Xu X (2022) Editorial: Temporal and Large-Scale Spatial Patterns of Plant Diversity and Diversification. Front. Ecol. Evol. 10:894234. doi: 10.3389/fevo.2022.894234
Received
11 March 2022
Accepted
04 May 2022
Published
18 May 2022
Volume
10 - 2022
Edited and reviewed by
Jairo Patiño, Spanish National Research Council (CSIC), Spain
Updates
Copyright
© 2022 Dimitrov, Neves and Xu.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Dimitar Dimitrov dimitard.gwu@gmail.comDanilo M. Neves dneves@icb.ufmg.brXiaoting Xu xiaotingxu@scu.edu.cn
This article was submitted to Biogeography and Macroecology, a section of the journal Frontiers in Ecology and Evolution
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.