- 1Department of Biodiversity and Conservation, Real Jardín Botánico (RJB), CSIC, Madrid, Spain
- 2Florida Museum of Natural History, University of Florida, Gainesville, FL, United States
- 3Department of Biology, Duke University, Durham, NC, United States
- 4Department of Botany, University of Innsbruck, Innsbruck, Austria
Editorial on the Research Topic
Understanding plant diversity and evolution in the Mediterranean Basin
The biota of the Mediterranean Basin (MB), characterized by a high species richness and endemism (Greuter, 1991; Blondel et al., 2010), has drawn the attention of biologists for centuries. While representing only 1.6% of Earth’s surface area, this hotspot of biodiversity houses 7–10% of the world’s plant diversity, 60% of which is restricted to the region (Myers et al., 2000; Thompson, 2005). Two main factors which have been shown to be important for high diversity in other Mediterranean climate zones–characterized by mild wet winters and warm dry summers– are low rates of extinction and an association with fire (Rundel et al., 2018). However, many additional features and forces shape biodiversity patterns in the MB (e.g., Nieto Feliner, 2014; Onstein et al., 2015).
Abiotic factors, in particular a complex and active geo-climatic history (Krijgsman, 2002; Rosenbaum et al., 2002), have played a crucial role in shaping the MB flora. Three climatic events are considered as fundamental historical landmarks in plant evolution within the region. These are the Messinian Salinity Crisis (MSC) c. 5.9 Ma (Bocquet et al., 1978), the advent of Mediterranean climate c. 3.2 Ma (Suc, 1984) and the climatic oscillations during the Pleistocene c. 2.5 Ma onwards (Hewitt, 2000). These abiotic events have been tested as drivers of diversification in numerous phylogenetic studies (e.g., Fiz-Palacios and Valcárcel, 2013; Crowl et al., 2015). However, in a biota as rich and diverse as that found in the MB, an accurate picture of diversification drivers across taxonomic groups and geographic areas requires consideration of additional factors. These include evolutionary consequential mechanisms such as polyploidy and hybridization (Thompson, 2005; Marques et al., 2018), the importance of annual habit and associated selfing reproduction (Stebbins, 1970), the heterogeneous orography that provided refugial areas in periods of adverse climates during the Pleistocene (Médail and Diadema, 2009), and the structure of the landscape, composed of a mosaic of habitat patches (Blondel et al., 2010). This structure could partly underlie features such as the importance of chasmophytic species (Davis, 1951), the role of ecological speciation (Thompson et al., 2005), in addition to shaping distribution limits of narrow endemics, which are highly represented in the MB (Thompson, 2005).
Another crucial factor that greatly influenced the MB biota across time is human impact. Flanking the fertile crescent, cradle of western civilizations, the impact of humans on the MB over, at least, the last 10,000 years has probably been the most intense on the planet leading to landscape modification, habitat destruction and species range fragmentation (Blondel et al., 2010; Thompson, 2020). In addition, the MB acted as a corridor for the rapid spread of useful wild species such as chestnut (Fineschi et al., 2000) or stone pine (Vendramin et al., 2008) and domesticated species or varieties (Zohary et al., 2012) although not always along an expected straight east-to-west direction, but rather involving the preservation of ancestral local lineages preceding agriculture (Besnard et al., 2018; Baumel et al., 2022).
Despite a considerable body of knowledge on plant evolution in the MB, we still have an insufficient understanding about the various potential drivers of diversification that, over time, have interacted with other numerous intervening factors to produce the rich plant biodiversity we observe. This is no doubt partly due to the complexity of the evolutionary history in the basin (Nieto Feliner, 2014). The present special issue is a reflection of the broad array of research foci and methodological approaches that the scientific community use to tackle the fascinating questions related to plant evolution in the MB.
Eight of the fifteen papers included in this special issue adopt macroevolutionary perspectives attempting to understand diversification patterns, taxonomic circumscriptions, and biogeographic connections of species lineages occurring in the MB and tested under explicit phylogenetic and phylogenomic frameworks. One of the factors generating uncertainty in taxonomy and phylogenetic relationships is polyploidy, which is documented in five of these studies. Cetlová et al. (2021) shows a combination of representative features for the MB in Alyssum, ranging from annual lifespan to multiple events of allopolyploidy, but also highlighting a strong human influence shaping its current distribution, and an impact of range shifts caused by sea-level changes, resulting in complex patterns. The same complexity is found in the Euphorbia nicaeensis alliance, which, as several other plant groups (e.g., Manafzadeh et al., 2014), colonized the MB from Western Asia and the Irano-Turanian region, and owes its partly unsettled taxonomy —including cryptic diversity— to diversification driven by vicariance in three main European Pleistocene refugia, ecological adaptation and, to a lesser extent, polyploidy (Stojilkovič et al., 2022). Polyploidy often evolves independently in different groups (Segraves et al., 1999). The following two studies identified different polyploidization patterns across the MB over time. Tomasello and Oberprieler (2022) find that elevational range shifts and secondary contact fostered allopolyploidy in Iberian populations of the genus Leucanthemopsis, whereas in other parts of its Mediterreanean-Alpine range, only autopolyploidy occurred. In the genus Centaurium, with tetraploids mainly distributed in northern temperate areas and hexaploids in southern arid areas, Maguilla et al. (2021) infer through diversification estimates, biogeographic analysis and chromosome evolution, that diploid lineages remained in the area of origin. By contrast, whole genome duplication events —recent and old— could have facilitated colonization and establishment in other areas. Aiming to tackle the complexity derived from polyploidy, Slenker et al. (2021) developed a new phylogenomic approach to identifying merged subgenomes from different progenitors, which allow them to infer an allopolyploid origin for the Greek endemic Cardamine barbaraeoides. Naciri et al. (2022) conclude that the chasmophyte habit, important in the MB, evolved independently several times in Silene sect. Italicae. The remaining two phylogenetic studies find high diversification rates: first, in the Iberian-centered genus Antirrhinum, associated with a geographic mode of speciation and multiple acquisition of key taxonomic characters (Otero et al., 2021); and second, in the Mediterranean lineage of Limonium, associated with the MSC, the onset of Mediterranean climate, Plio-Pleistocene sea-level fluctuations, and apomixis (Koutroumpa et al., 2021).
In line with the diversity of possible evolutionary outcomes, hybridization can be addressed under different approaches. The contribution by López de Heredia et al. (2021) exemplifies how in two hybridizing species of the best known syngameon —Quercus (Cannon and Petit, 2020)— cytonuclear incompatibilities may have shaped the combination of plastid and nuclear genomes across the species ranges. Abdelaziz et al. provide evidence of a stable unimodal hybrid zone in the genus Erysimum, one of the possible evolutionary outcomes of hybridization, which however has been insufficiently studied in plants (Abbott, 2017).
One of the unwritten goals of the present special issue was to enrich our knowledge concerning the Balkan Peninsula, a critical area for the evolution of MB biota, as well as for the postglacial recolonization of central Europe (Hewitt, 2011). In addition to Slenker et al. (2021), four other papers focused on this region. Rešetnik et al. (2022) and Torre et al. (2022) unveil the role of the Balkans as a cradle of diversification and a source for dispersal into other areas in Aurinia saxatilis and Ulmus laevis, respectively. Lazarević et al. (2022) explore the consequences of interploidy hybridization in the areas of contact between two Tertiary relict species of the long-lived genus Ramonda using AFLPs and genome size estimation. Using an integrative approach that includes environmental modelling, Faltner et al. (2023) provide clues to the causes behind very narrowly-distributed endemics in the MB and clarify the unforeseen phylogenetic position of one of them. Focusing on Euphorbia orphanidis, an endangered species restricted to a few patches of limestone screes in Mt. Parnassos (Greece), this study underlines the role of microrelief in heterogeneous mountain environments. Finally, a phylogeographic study focuses on a narrow endemic coastal species, Eokochia saxicola, which is exceptional in the MB for being wind-pollinated, and concludes that, despite small population sizes, this rare species does not face immediate conservation risks (Strumia et al., 2021).
The Mediterranean Basin is undoubtedly a remarkable biogeographic region with a rich but fragile flora. We hope that this collection of studies provides the inspiration and motivation for much needed additional research in this biodiversity hotspot.
Author contributions
All authors listed have made a substantial, direct and intellectual contribution to the work, and approved it for publication.
Funding
This study was supported by grant MCIN/ AEI/ FEDER (PID2021-125432NB-I00), from the Spanish Ministry of Science and Innovation, to GNF.
Acknowledgments
We thank all reviewers, who have helped us edit the articles included in this Research Topic.
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.
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.
References
Abbott, R. J. (2017). Plant speciation across environmental gradients and the occurrence and nature of hybrid zones. J. Syst. Evol. 55, 238–258. doi: 10.1111/jse.12267
Baumel, A., Nieto Feliner, G., Médail, F., La Malfa, S., Di Guardo, M., Bou Dagher Kharrat, M., et al. (2022). Genome-wide footprints in the carob tree (Ceratonia siliqua) unveil a new domestication pattern of a fruit tree in the Mediterranean. Mol. Ecol. 31, 4095–4111. doi: 10.1111/mec.16563
Besnard, G., Terral, J. F., Cornille, A. (2018). On the origins and domestication of the olive: A review and perspectives. Ann. Bot.-London 121, 385–403. doi: 10.1093/aob/mcx145
Blondel, J., Aronson, J., Bodiou, J. Y., Boeuf, G. (2010). The Mediterranean region: biological diversity in space and time (New York: Oxford University Press).
Bocquet, G., Widler, B., Kiefer, H. (1978). The messinian model, a new outlook for the floristics and systematics of the Mediterranean area. Candollea 33, 269–287.
Cannon, C. H., Petit, R. J. (2020). The oak syngameon: more than the sum of its parts. New Phytol. 226, 978–983. doi: 10.1111/nph.16091
Crowl, A. A., Visger, C. J., Mansion, G., Hand, R., Wu, H.-H., Kamari, G., et al. (2015). Evolution and biogeography of the endemic Roucela complex (Campanulaceae: Campanula) in the Eastern Mediterranean. Ecol. Evol. 5, 5329–5343. doi: 10.1002/ece3.1791
Davis, P. H. (1951). Cliff vegetation in the eastern Mediterranean. J. Ecol. 39, 63–93. doi: 10.2307/2256628
Fineschi, S., Taurchini, D., Villani, F., Vendramin, G. G. (2000). Chloroplast DNA polymorphism reveals little geographical structure in Castanea sativa mill. (Fagaceae) throughout southern European countries. Mol. Ecol. 9, 1495–1503. doi: 10.1046/j.1365-294x.2000.01029.x
Fiz-Palacios, O., Valcárcel, V. (2013). From messinian crisis to Mediterranean climate: a temporal gap of diversification recovered from multiple plant phylogenies. Perspect. Plant Ecol. 15, 130–137. doi: 10.1016/j.ppees.2013.02.002
Greuter, W. (1991). Botanical diversity, endemism, rarity, and extinction in the Mediterranean area: an analysis based on the published volumes of med-checklist. Bot. Chron. 10, 63–79.
Hewitt, G. M. (2000). The genetic legacy of the quaternary ice ages. Nature 405, 907–913. doi: 10.1038/35016000
Hewitt, G. M. (2011). “Mediterranean Peninsulas: the evolution of hotspots,” in Biodiversity hotspots. Eds. Zachos, F. E., Habel, J. C. (Berlin, Heidelberg: Springer), 123–147.
Krijgsman, W. (2002). The Mediterranean: Mare nostrum of earth sciences. Earth Planet. Sc. Lett. 205, 1–12. doi: 10.1016/S0012-821X(02)01008-7
Manafzadeh, S., Salvo, G., Conti, E. (2014). A tale of migrations from east to west: The irano-turanian floristic region as a source of Mediterranean xerophytes. J. Biogeogr. 41, 366–379. doi: 10.1111/jbi.12185
Marques, I., Loureiro, J., Draper, D., Castro, M., Castro, S. (2018). How much do we know about the frequency of hybridisation and polyploidy in the Mediterranean region? Plant Biol. 20, 21–37. doi: 10.1111/plb.12639
Médail, F., Diadema, K. (2009). Glacial refugia influence plant diversity patterns in the Mediterranean basin. J. Biogeogr. 36, 1333–1345. doi: 10.1111/j.1365-2699.2008.02051.x
Myers, N., Mittermeier, R. A., Mittermeier, C. G., da Fonseca, G. A. B., Kent, J. (2000). Biodiversity hotspots for conservation priorities. Nature 403, 853–858. doi: 10.1038/35002501
Nieto Feliner, G. (2014). Patterns and processes in plant phylogeography in the Mediterranean basin. A review. Perspect. Plant Ecol. 16, 265–278. doi: 10.1016/j.ppees.2014.07.002
Onstein, R. E., Carter, R. J., Xing, Y., Richardson, J. E., Linder, H. P. (2015). Do Mediterranean-type ecosystems have a common history?–insights from the buckthorn family (Rhamnaceae). Evolution 69, 756–771. doi: 10.1111/evo.12605
Rosenbaum, G., Lister, G. S., Duboz, C. (2002). Reconstruction of the tectonic evolution of the western Mediterranean since the oligocene. J. Virtual Explor. 8, 107–130. doi: 10.3809/jvirtex.2002.00053
Rundel, P. W., Arroyo, M. T., Cowling, R. M., Keeley, J. E., Lamont, B. B., Pausas, J. G., et al. (2018). Fire and plant diversification in Mediterranean-climate regions. Front. Plant Sci. 9. doi: 10.3389/fpls.2018.00851
Segraves, K. A., Thompson, J. N., Soltis, P. S., Soltis, D. E. (1999). Multiple origins of polyploidy and the geographic structure of Heuchera grossulariifolia. Mol. Ecol. 8, 253–262. doi: 10.1046/j.1365-294X.1999.00562.x
Stebbins, G. L. (1970). Adaptive radiation of reproductive characteristics in angiosperms, i. pollination mechanisms. Annu. Rev. Ecol. Syst. 1, 307–326. doi: 10.1046/j.1365-294X.1999.00562.x
Suc, J. P. (1984). Origin and evolution of the Mediterranean vegetation and climate in Europe. Nature 307 (5950), 429–432. doi: 10.1038/307429a0
Thompson, J. D. (2020). Plant evolution in the Mediterranean: insights for conservation (USA: Oxford University Press).
Thompson, J. D., Lavergne, S., Affre, L., Gaudeul, M., Debussche, M. (2005). Ecological differentiation of Mediterranean endemic plants. Taxon 54, 967–976. doi: 10.2307/25065481
Vendramin, G. G., Fady, B., González-Martínez, S. C., Hu, F. S., Scotti, I., Sebastiani, F., et al. (2008). Genetically depauperate but widespread: the case of an emblematic Mediterranean pine. Evolution 62, 680–688. doi: 10.1111/j.1558-5646.2007.00294.x
Keywords: Mediterranean Basin, systematics, evolution, biogeography, phylogeography, phylogenetics, hybridization, polyploidy
Citation: Nieto Feliner G, Cellinese N, Crowl AA and Frajman B (2023) Editorial: Understanding plant diversity and evolution in the Mediterranean Basin. Front. Plant Sci. 14:1152340. doi: 10.3389/fpls.2023.1152340
Received: 27 January 2023; Accepted: 07 February 2023;
Published: 14 February 2023.
Edited and Reviewed by:
Susann Wicke, Humboldt University of Berlin, Berlin, GermanyCopyright © 2023 Nieto Feliner, Cellinese, Crowl and Frajman. 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: Gonzalo Nieto Feliner, bmlldG9AcmpiLmNzaWMuZXM=