Next Article in Journal
Salmonidae Genome: Features, Evolutionary and Phylogenetic Characteristics
Next Article in Special Issue
Transcriptome Level Reveals the Triterpenoid Saponin Biosynthesis Pathway of Bupleurum falcatum L.
Previous Article in Journal
Effects of Tributyrin Supplementation on Liver Fat Deposition, Lipid Levels and Lipid Metabolism-Related Gene Expression in Broiler Chickens
Previous Article in Special Issue
Characterization of the Evolutionary Pressure on Anisodus tanguticus Maxim. with Complete Chloroplast Genome Sequence
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Genes
Volume 13
Issue 12
10.3390/genes13122220
genes-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Interplay of Ecological Opportunities and Functional Traits Drives the Evolution and Diversification of Millettiod Legumes (Fabaceae)

by
Dongzhu Jiang
†,
Linzheng Liao
†,
Haitao Xing
,
Zhidan Chen
,
Xuemei Luo
and
Hong-Lei Li
*
College of Landscape Architecture and Life Science/Institute of Special Plants, Chongqing University of Arts and Sciences, Chongqing 402168, China
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Genes 2022, 13(12), 2220; https://doi.org/10.3390/genes13122220
Submission received: 27 October 2022 / Revised: 22 November 2022 / Accepted: 22 November 2022 / Published: 27 November 2022
(This article belongs to the Special Issue Phylogenetics, Genetics, and Breeding of Medicinal Plants)
Browse Figures
Versions Notes

Abstract

:
Understanding the striking diversity of the angiosperms is a paramount issue in biology and of interest to biologists. The Millettiod legumes is one of the most hyper-diverse groups of the legume family, containing many economically important medicine, furniture and craft species. In the present study, we explore how the interplay of past climate change, ecological opportunities and functional traits’ evolution may have triggered diversification of the Millettiod legumes. Using a comprehensive species-level phylogeny from three plastid markers, we estimate divergence times, infer habit shifts, test the phylogenetic and temporal diversification heterogeneity, and reconstruct ancestral biogeographical ranges. We found that three dramatic accumulations of the Millettiod legumes occurred during the Miocene. The rapid diversification of the Millettiod legumes in the Miocene was driven by ecological opportunities created by the emergence of new niches and range expansion. Additionally, habit shifts and the switch between biomes might have facilitated the rapid diversification of the Millettiod legumes. The Millettiod legumes provide an excellent case for supporting the idea that the interplay of functional traits, biomes, and climatic and geographic factors drives evolutionary success.

1. Introduction

Angiosperms are the most prominent life form across global ecosystems, and exhibit a spectacular range of morphological and ecological diversity on the Earth [1]. However, the species diversity across the Tree of Life of the angiosperms is uneven. Understanding the striking diversity of the angiosperms is a paramount issue in biology and of interest to biologists [1,2,3]. Previous studies found that the rapid radiations of many angiosperm groups was driven by both biological (intrinsic) and environmental (extrinsic) factors [4,5,6,7]; however, the effects of functional traits, the biome, and climatic and geographic factors on plant diversification are largely unknown.
The Millettiod legumes is one of the most hyper-diverse groups in the legume family. This clade is composed of five tribes (Millettieae, Abreae, Phaseoleae, Desmodieae and Psoraleeae), including more than 2600 described species with a global distribution [8,9]. The Millettiod legumes contain many economically important species, which contribute enormously to the word’s economy through food and vegetables, pharmaceuticals and medicines, furniture and crafts, chemicals and fertilizers, as well as horticulture [9]. The main dietary legumes include pigeon pea (Cajanus cajan Millsp.), soybean (Glycine max Merr.), cowpea (Vigna unguiculata Walp.), and bean (Phaseolus). Vetches (Vicia amoena Fisch.) and tropical kudzu (Pueraria phaseoloides Benth.) were important pastures used for forage. Species such as Desmodium, Macoptilium and Centrosema are used for the purpose of improving tropical pasture systems [10]. Showy-flowered species of Mucuna and Strongylodon are very popular in tropical gardens. Species of Erythrina are important woody tree legumes in forestry. Multipurpose shrubs, such as Butea and Millettia, are regional favorites as ornaments and for shade [9].
The Millettiod legumes show great diversity in their morphological and habit characteristics from ephemeral herbs and herbaceous climbers to shrubs, woody lianas and trees. The terminal taxa of the Millettiod legumes grow in various habitats such as succulent, grass, rainforest and temperate, which are in accordance with major zonobiomes [9,11]. The crown age of the Millettiod legumes is 44.1 Ma to 53 Ma. Global climate and tectomic changes since the Eocene may have triggered the diversification of many angiosperm lineages [12,13,14,15,16]. Moreover, the diversification of Psoraleeae is assumed to be a result of global climate change during the Pleistocene [17]. The evolution of phaseoloid legumes may be due to habit shifts and dispersal events along with the global climate changes since the Oligocene [18]. However, it remains puzzling and unexplored how the evolution of habits fostered diversification in the Millettiod legumes and how ecological forces have been regulating cladogenesis in different geographical areas.
A well-resolved phylogeny of Millettiod legumes is paramount for understanding the aspects of the temporal and biogeographical patterns of diversification. Some previous molecular phylogenetic studies have made progress in the delimitation of the Millettiod legumes based on nuclear ribosomal ITS or a few plastid loci [18,19,20,21,22]. These researches generated a well-resolved phylogenetic framework of the Millettiod legumes at tribal levels [3,23]. However, less than 40% of the generic diversity of the Millettiod legumes was sampled in previous studies. Therefore, a well-resolved phylogeny with dense taxon sampling at species level is needed to understand the evolutionary dynamics of the Millettiod legumes. Oyebanji et al. proved that plastome is an effective marker for resolving the evolutionary relationships of the Millettiod legumes [23]. In the past decades, plastome data of the Millettiod legumes increased rapidly along with previous studies [19,20,21,22,24,25,26,27]. The data accumulation of the Millettiod legumes provides an opportunity to reconstruct the phylogeny of this clade with comprehensive taxon sampling.
In the present study, we first reconstruct a species-level phylogeny for the phaseoloid legumes using three plastid loci with a more extensive generic sampling than in any previous studies. Based on the improved phylogenetic framework, we then explore how the interplay of past climate change, geographical expansion and habit shifts may have triggered diversification of the Millettiod legumes.

2. Material and Methods

2.1. Taxon and Nuclear Marker Sampling

Three plastid regions (rbcL, matK and trnL-F) were selected as DNA markers for the phylogenetic analyses of the Millettiod legumes. The combination of these three plastid regions has been proved to have high-efficiency in resolving intergeneric and interspecific relationships. To obtain dense sampling of the Millettiod legumes, all available nucleotide sequences of these three markers from GenBank were collected firstly. Then, sequences were filtered following the principles: (1) For each taxon, the same species and DNA sample across three plastid markers were kept in priority, but some composite accessions were necessary to represent genera. (2) When multiple sequences were available for each marker, the longest sequence was retained. (3) In the scenario of multiple sequences with the same length, one sequence was randomly selected. (4) In a genus, when one marker occurred in species different with other markers, the species with faster evolved marker were kept following the order: trnL-F, rbcL, matK. All the works above were completed by using a series of R scripts written by our group. Most of the DNA sequences have been used in previously published studies [19,20,21,22,24,25,26,27]. Species names and GenBank accession numbers are listed in Table S1.

2.2. Alignment and Phylogeny

For the two DNA coding genes (rbcL and matK), sequences were aligned directly in the program MUSCLE with the default settings [28]. Then the aligned matrix was manually adjusted using BioEdit version 5.0.9 (Hall, T.A., California, USA) [29]. For the plastid region trnL-F, sequences were aligned using a two-step strategy. First, sequences were divided into clusters according to taxonomic unit and aligned in the program MUSCLE under default high accuracy parameters with subsequently manual adjustment. Then, the matrix of each cluster was aligned using the profile–profile alignment algorithm in MUSCLE and final adjustments were made to the alignments using the refinement algorithm in MUSCLE. Alignment of each plastid region was manually trimmed for quality and maximum coverage. The final aligned matrix contains 429 OTUs.
To check the conflicts among three plastid regions, the initial phylogenetic analysis for each marker was carried out using maximum likelihood (ML) method implemented in the program RAxML version 7.6.6 (Stamatakis, A., Lausanne, Switzerland) [30]. After checking for significant conflict among different nodes (bootstrap support value exceeding 70%), all data from different markers were combined for further analyses. We used the ML method to construct the phylogeny of the Millettiod legumes based on the combined data. The ML analysis was performed using RAxML with the following options: three data partitions (rbcL, matK and trnL-F), GTR + I + G nucleotide substitution model, and gaps treated as missing data. A standard bootstrap analysis with 1000 bootstrap iterations was used to estimate the branch support. The program was run on the CIPRES network [31].

2.3. Molecular Dating

To date the branching events within the Millettiod legumes, a Bayesian MCMC approach as implemented in BEAST version 1.8.0 (Drummond, A.J., Auckland, Zealand) was used based on the combined dataset of 429 terminals [32]. We selected 7 calibration points from the result of Lavin et al. [33]. These calibration points could be confidently assigned to clades and nodes represented in our dataset (Table S2). A normal distribution was used for all 7 calibration points. The standard deviation was set to contain the lower and higher boundaries of the 95% highest posterior density values. MCMC searches were run for 500,000,000 generations, sampled every 5000 generations. Tracer v1.5 was used to monitor appropriate burn-in and the adequate effective sample sizes of the posterior distribution (>200). The maximum clade credibility tree was computed by TreeAnnotator v1.7.5 in BEAST software package [34]. BEAST analyses were performed in the CIPRES Web Portal 3.1 (Miller, M.A., California, USA) [31].

2.4. Trait Evolution Analyses

To clarify the trait evolutionary history of the Millettiod legumes, the habit and biome information were collected (Table S2). The habit information of the Millettiod legumes was collected from International Legume Database & Information Service (ILDIS). Two habit states were coded, herbaceous (including herbs and herbaceous climbing vines) vs. woody (including trees, woody climbers and shrubs) (Table S1). According to the geographic distributions and the biome patterns of Lewis et al. [9], five biome types were coded: (1) succulent (S), including semi-arid, non-fire-adapted, succulent-rich and grass-poor, dry tropical forest, thicket and bushland biome; (2) grass (G), comprising a fire-adapted, succulent-poor and grass-rich, seasonally dry tropical forest, woodland and savanna biome; (3) rainforest (R), comprising the equatorial tropics (wet forests) worldwide; (4) temperate north (TN), comprising the Mediterranean, warm and cold temperate regions of the North Hemisphere; and (5) temperate south (TS), comprising the area except for the first three biomes (Table S1). The parsimony method implemented in Mesquite v2.74 was used to reconstruct the trait evolution of the Millettiod legumes [35]. The maximum clade credibility tree obtained from the Bayesian analysis was used as input tree.

2.5. Diversification Analyses

To visualize the temporal dynamics of the diversification rates in the Millettiod legumes, we constructed the semilogarithmic lineage-through-time (LTT) plots using the R package APE v2.5-1 [36]. In total, 1000 dated phylogenies obtained from the Bayesian analyses were randomly selected and used to generate semilogarithmic LTT plots. To verify the rapid shifts in diversification rates at any specified time, the RC statistic was performed using the R package GEIGER v1.3-1 [37]. We used 11 models including pureBirth, bd, DDX, DDL, SPVAR, EXVAR, BOTHVAR, yule2rate, yule3rate, yule4rate and yule5rate to assess the significant rate changes. A diversification rate shift was confirmed by the criterion that more or fewer descendants than expected under the constant rate model happen in lineages.

2.6. Biogeographical Analyses

In order to infer the possible ancestral ranges of the Millettiod legumes, a Bayes-DIVA analysis [38] was conducted using the software package RASP [39]. Bayes-DIVA method is a popular method with the advantages of minimizing the phylogenetic uncertainties and generating credibility support values for alternative phylogenetic relationships [38,39]. We used 1000 trees from the BEAST output as a “trees file”. The maximum clade credibility tree was used as a final representative tree. With the aim of predicating the ancestral areas of nodes deeper down into the tree, biogeographical analyses were run on continental spatial scale at species level. According to Lewies et al. [9] and the ILDIS database, nine geographic regions were coded: A, Africa; B, Asia; C, Australia; D, Indian Ocean area, including islands in the Indian Ocean region and Madagascar; E, Pacific, including islands in the Pacific; F, North America; H, Central America; I, Europe; K, South America (Table S1). The “maxareas” was constrained to 3 when constructing the ancestral areas of the Millettiod legumes.

3. Results

3.1. Phylogeny of the Millettiod Legumes

The aligned matrix of the combined three-marker dataset consists of 4728 characters with 2290 variable and 1690 parsimony-informative sites. The tree generated by the maximum likelihood (ML) analysis (Figure S1) was highly consistent with those retrieved from the Bayesian inference (BI) analysis (Figure S2), except for some weakly supported nodes (BS < 70%). The Millettiod legumes are strongly supported as monophyletic (BS 100%, PP 1.0). Within the Millettiod legumes, five major clades were identified: Basal millettioid (BS 94%, PP 1.0), Clitoriinae (BS 59%, PP 0.87), Disynstemon + (Abreae + (Diocleinae + core Millettieae)) (BS 81%, PP 1.0), Platycyamus + Dewevrea (BS 91%, PP 1.0), and the phaseoloid clade (BS 98%, PP 1.0). Within the phaseoloid clade, Desmodieae, Cajaninae and Phaseolinae are monophyletic with high support. Psoraleeae is monophyletic and nested in Glycininae.

3.2. Divergence-Time Estimates of the Millettiod Legumes

Based on our analyses, the Millettiod legumes diversified at 45.1 Ma (42.3–47.3 Ma, HPD) (Figure 1 and Figure S3). The second lineage separated from the remaining Millettiod legumes at 44.5 Ma (40.1–45.6 Ma, HPD). The tribe Abreae split with its sister lineage at 34.3 Ma (32.2–38.2 Ma, HPD). The divergence time between core Millettieae and Diocleinae was estimated to be 27.3 Ma (26.4–35.4 Ma, HPD). The steam age of the phaseoloid clade was 37.3 Ma (36.1–41.4 Ma, HPD), and the crow age was 31.1 Ma (28.8–33.5 Ma, HPD). Desmodieae diverged from its close relatives at 24.8 Ma (23.7–30.0 Ma, HPD). Psoraleeae separated from Glycine at 11.8 Ma (8.8–14.4 Ma, HPD).

3.3. Trait Evolution

Results of the ancestral habit state reconstruction of the Millettiod legumes are shown in Figure 2. The ancestral state of the Millettiod legumes was woody. Multiple transitions between woody and herbaceous occurred during the evolutionary history of the Millettiod legumes. Our results showed that switching frequency from woody to herbaceous was higher than that from herbaceous. The switching frequency from woody to herbaceous was 52, whereas the switching frequency from herbaceous to woody was 25. In our examining transitions analyses among biomes, the common ancestor of the Millettiod legumes was most likely distributed in a grass biome (Figure 3). The ancestor of core Millettieae similarly may have occupied a grass biome with subsequent shifts into the other biome types. The ancestor of the phaseoloid clade was also distributed in a grass biome. Multiple shifts between biome types in different clades were detected since the Miocene.

3.4. Reconstruction of Historical Biogeography

The results of biogeographic reconstruction are summarized in Figure 1 and Figure S4. The most recent common ancestor (MRCA) of the Millettiod legumes was equivocal, either in Africa (p = 0.44), Asia (p = 0.39) or the other regions (p = 0.17). Multiple colonization events occurred independently during the evolutionary history of the Millettiod legumes. The MRCA of core Millettieae was Africa (p = 0.88), and dispersed from Africa to Asia, North America, Central America and South America multiple times. The MRCA of the phaseoloid legumes occurred in Asia (p = 0.84), with a number of movements into Africa, Australia and Central America. Among all of the nine geographic regions, Africa and Asia harbored higher frequency of lineage emigration (185 and 204 times, respectively) than immigration (73 and 90 times, respectively). Conversely, the frequency of lineage emigration in Australia, the Indian Ocean area and Pacific harbor was lower with the numbers being 17, 10 and 17.5, respectively, whereas the frequencies of lineage immigration were 81, 87 and 69, respectively.

3.5. Diversification Rates

Our results of the semilogarithmic lineage-through-time (LTT) showed that the Millettiod legumes experienced a high diversification rate in the Miocene (Figure 4). When testing the significant rate changes based on 11 models, the AIC values of seven constant rate models, including pureBirth, bd, DDX, DDL, SPVAR, EXVAR and BOTHVAR, were found to be higher than the other four and were excluded (Table 1). Among the variable rate models, the AIC value of yule5rate was the lowest and was selected as the best fit model for the diversification rate analyses of the Millettiod legumes. Three rapid increases in diversification rate were found in the Millettiod legumes: the first was at 17.78 Ma with a rate change from 0.07 to 0.13 (sp Myr−1); the second was at 11.57 Ma, with a rate change from 0.13 to 0.29 (sp Myr−1); the third was at 8.46 Ma, with a rate change from 0.10 to 0.19 (sp Myr−1).

4. Discussion

Reliable molecular dating is an essential precondition for revealing the diversification patterns of plant lineages. Phylogenetic analyses of the combined three-region DNA dataset generated a well-supported evolutionary framework of the Millettiod legumes (Figure 1, Figures S1 and S2). The relationships among the main lineages of the Millettiod legumes were in accordance with previous studies [3,18,21,22,23]. Based on our time estimates, the crown age of the Millettiod legumes was 45.1 Ma (42.3–47.3 Ma, HPD; Figure 1 and Figure S3), which corresponded to previous studies [1,33]. The crown age of the phaseoloid legumes was 31.1 Ma (28.8–33.5 Ma, HPD), which was consistent with the estimations of many previous studies [18,26,33]. Our result showed the crown age of Psoraleeae was 5.6 Ma (4.29–8.4 Ma, HPD), which was in accordance with the result of Egan and Crandall [17]. All these results indicated that the divergence times of the Millettiod legumes in the present study were credible.
Our biogeographic reconstruction and dating analyses indicated the Millettiod legumes occurred in Africa (p = 0.44) or Asia (p = 0.39) in the early Eocene. The LTT plot indicated that a dramatic burst of diversification of the Millettiod legumes occurred during the Miocene (c. 18–8 Ma; Figure 4). Three dramatic accumulations of the Millettiod legumes were detected at 17.8 Ma, 11.6 Ma and 8.5 Ma (Table 1). In accordance with the diversification patterns, high frequent migrations of the Millettiod legumes did not occur until the Miocene after its origin with the exception of some dispersal events into Central America and South America (clade Clitoriinae). Multiple colonization events seem to have occurred within a 10-million-year time window (c. 18–8 Ma, Figure 1). The ancestor of the Diocleinae experienced dispersal events into Central America, South America and the Pacific. There were at least three dispersal events into Central America and South America for the core Millettieae, and two such movements into the Indian Ocean area (Figure 1 and Figure S4). Additionally, the Phaseoloids clade experienced multiple dispersal events from Africa to Central America. In the Miocene, the Qinghai–Tibetan Plateau experienced multiple stages of uplift with a rapid uplift at 10–7 Ma [40,41,42,43,44]. The African plate collided with the Eurasian at ca. 18–17 Ma [45]. In the southern hemisphere, the thrust of the South American plate against the Pacific plate led to the rise of the Andes mountains [46]. These geological events fragmented the ecosystems and subsequently opened many new niches [47,48], and forced the rapid diversification of many plant lineages [16,49,50,51,52,53]. Thus, our finding suggests that the rapid diversification of the Millettiod legumes in the Miocene was driven by ecological opportunities created by the emergence of new niches and range expansion.
In the Miocene, the global climate tended to be cooler, drier and more seasonal [54,55,56]. Both Asia and America experienced an arid period of marked aridity due to orogenetic changes [57,58,59,60]. The African plate also experienced an analogous arid period of aridity due to the closure of the Tethys Sea [45,61]. Our trait evolution analyses showed that a larger number of lineages in the 10-million-year time window (c. 18–8 Ma) were herbaceous and inhabited a grass biome. The grass biome generally has a unimodal rainfall pattern, which comprises a fire-adapted, succulent-poor and grass-rich, seasonally dry tropical forest, woodland and savanna [9,11]. The extensive aridity could have promoted the diversification of some groups inhabiting dry regions, such as Bursera [62] and the Potentilla [63]. Herbs could have produced higher per-year mutation rates on the basis of a shorter generation time, consequentially contributing to the adaptation of herbaceous lineages to dry climates [64,65,66]. Additionally, multiple shifts from the grass biome to other biomes, especially the rainforest biome, were found in the Miocene. The interdigitation of the grass and the rainforest biome favors a “refuge” interpretation of allopatric divergence, which was caused by the contraction and expansion of dry-adapted and wet vegetation [67]. Taxa adapted to different biomes are always pioneer species, which can take advantage most effectively of post-disturbance conditions [9]. Thus, the expansion of arid lands due to orogenetic and climatic changes increased the arid niche space, and the switch between biomes might have facilitated the rapid diversification of the Millettiod legumes during the Miocene.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/genes13122220/s1, Figure S1. Phylogenetic relationships of the phaseoloid legumes using maximum-likelihood (ML) method; Figure S2. Phylogenetic relationships of the phaseoloid legumes using Bayesian inference (BI) method; Figure S3. Chronogram for the Millettiod legumes obtained under a Bayesian relaxed clock; Figure S4. Biogeographic analysis of the Millettiod legumes by Statistical Dispersal-Vicariance Analysis (S-DIVA).; Table S1. Taxa, GenBank accession numbers, Life form code and Biome code for samples included in this study; Table S2. Calibrations used in this study. Node number followed Lavin et al., 2005.

Author Contributions

H.-L.L. conceived the study. D.J., L.L., H.X., Z.C. and X.L. performed the experiments. H.-L.L., D.J. and L.L. analyzed the data. H.-L.L., D.J., L.L. and Z.C. contributed reagents/materials/analysis tools. H.-L.L., D.J. and L.L. wrote the paper. H.-L.L. and D.J. edited the paper. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported by National Natural Science Foundation of China (No. 31500175 and 32270237), and the Foundation for High-level Talents of Chongqing University of Arts and Science (2017RTZ21, P2018TZ05).

Informed Consent Statement

Not applicable.

Acknowledgments

We would like to thank Miaoqin Xia, Xavier-ravi Baskaran and Zhiduan Chen for helping to read and revise the manuscript; Min Gong modified the Figures.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Lu, L.M.; Mao, L.F.; Yang, T.; Ye, J.F.; Liu, B.; Li, H.L.; Sun, M.; Miller, J.T.; Mathews, S.; Hu, H.H. Evolutionary history of the angiosperm flora of China. Nature 2018, 554, 234–238. [Google Scholar] [CrossRef]
  2. Huang, W.; Zhang, L.; Columbus, J.T.; Hu, Y.; Zhao, Y.; Tang, L.; Guo, Z.; Chen, W.; McKain, M.; Bartlett, M. A well-supported nuclear phylogeny of Poaceae and implications for the evolution of C4 photosynthesis. Mol. Plant 2022, 15, 755–777. [Google Scholar] [CrossRef]
  3. Zhao, Y.; Zhang, R.; Jiang, K.W.; Qi, J.; Hu, Y.; Guo, J.; Zhu, R.; Zhang, T.; Egan, A.N.; Yi, T.S. Nuclear phylotranscriptomics and phylogenomics support numerous polyploidization events and hypotheses for the evolution of rhizobial nitrogen-fixing symbiosis in Fabaceae. Mol. Plant 2021, 14, 748–773. [Google Scholar] [CrossRef] [PubMed]
  4. Givnish, T.J.; Spalink, D.; Ames, M.; Lyon, S.P.; Hunter, S.J.; Zuluaga, A.; Iles, W.J.; Clements, M.A.; Arroyo, M.T.; Leebens-Mack, J. Orchid phylogenomics and multiple drivers of their extraordinary diversification. Proc. R. Soc. B 2015, 282, 20151553. [Google Scholar] [CrossRef]
  5. Bouchena-Khelladi, Y.; Onstein, R.E.; Xing, Y.; Schwery, O.; Linder, H.P. On the complexity of triggering evolutionary radiations. N. Phytol. 2015, 207, 313–326. [Google Scholar] [CrossRef] [PubMed]
  6. Hughes, C.E.; Atchison, G.W. The ubiquity of alpine plant radiations: From the Andes to the Hengduan Mountains. N. Phytol. 2015, 207, 275–282. [Google Scholar] [CrossRef] [PubMed]
  7. Simões, M.; Breitkreuz, L.; Alvarado, M.; Baca, S.; Cooper, J.; Heins, L.; Herzog, K.; Lieberman, B. The evolving theory of evolutionary radiations. Trends Ecol. Evol. 2016, 31, 27–34. [Google Scholar] [CrossRef]
  8. Schrire, B.D.; Lavin, M.; Barker, N.P.; Forest, F. Phylogeny of the tribe Indigofereae (Leguminosae Papilionoideae): Geographically structured more in succulent-rich and temperate settings than in grass-rich environments. Am. J. Bot. 2009, 96, 816–852. [Google Scholar] [CrossRef]
  9. Lewis, G.; Schrire, B.; MacKinder, B.; Lock, M. Legumes of the World; Royal Botanic Gardens: Kew, UK, 2005. [Google Scholar]
  10. Graham, P.H.; Vance, C.P. Legumes: Importance and constraints to greater use. Plant Physiol. 2003, 131, 872–877. [Google Scholar] [CrossRef] [Green Version]
  11. Breckle, S.W. Walter’s Vegetation of the Earth: The Ecological Systems of the Geo Biosphere; Springer: Berlin/Heidelberg, Germany, 2002. [Google Scholar]
  12. Wade, B.; Pälike, H. Oligocene climate dynamics. Paleoceanography 2004, 19, PA4019. [Google Scholar] [CrossRef]
  13. Palike, H.; Norris, R.D.; Herrle, J.O.; Wilson, P.A.; Coxall, H.K.; Lear, C.H.; Shackleton, N.J.; Tripati, A.K.; Wade, B.S. The heartbeat of the Oligocene climate system. Science 2006, 314, 1894–1898. [Google Scholar] [CrossRef] [Green Version]
  14. Lu, H.; Guo, Z. Evolution of the monsoon and dry climate in East Asia during late Cenozoic: A review. Sci. China Earth Sci. 2014, 57, 70–79. [Google Scholar] [CrossRef]
  15. Tada, R.; Zheng, H.; Clift, P.D. Evolution and variability of the Asian monsoon and its potential linkage with uplift of the Himalaya and Tibetan Plateau. Prog. Earth Planet. Sci. 2016, 3, 4. [Google Scholar] [CrossRef] [Green Version]
  16. Zhao, J.L.; Gugger, P.F.; Xia, Y.M.; Li, Q.J. Ecological divergence of two closely related Roscoea species associated with late Quaternary climate change. J. Biogeogr. 2016, 43, 1990–2001. [Google Scholar] [CrossRef]
  17. Egan, A.N.; Crandall, K.A. Divergence and diversification in North American Psoraleeae (Fabaceae) due to climate change. BMC Biol. 2008, 6, 55. [Google Scholar] [CrossRef] [Green Version]
  18. Li, H.; Wang, W.; Lin, L.; Zhu, X.; Li, J.; Zhu, X.; Chen, Z. Diversification of the phaseoloid legumes: Effects of climate change, range expansion and habit shift. Front. Plant Sci. 2013, 4, 386. [Google Scholar] [CrossRef] [Green Version]
  19. Kajita, T.; Ohashi, H.; Tateishi, Y.; Bailey, C.D.; Doyle, J.J. RbcL and legume phylogeny, with particular reference to Phaseoleae, Millettieae, and allies. Syst. Bot. 2001, 26, 515–536. [Google Scholar]
  20. Cardoso, D.; de Queiroz, L.P.; Pennington, R.T.; de Lima, H.C.; Fonty, É.; Wojciechowski, M.F.; Lavin, M. Revisiting the phylogeny of papilionoid legumes: New insights from comprehensively sampled early branching lineages. Am. J. Bot. 2012, 99, 1991–2013. [Google Scholar] [CrossRef] [PubMed]
  21. Azani, N.; Babineau, M.; Bailey, C.D.; Banks, H.; Barbosa, A.R.; Pinto, R.B.; Boatwright, J.S.; Borges, L.M.; Brown, G.K.; Bruneau, A.; et al. A new subfamily classification of the Leguminosae based on a taxonomically comprehensive phylogeny. Taxon 2017, 66, 44–77. [Google Scholar] [CrossRef] [Green Version]
  22. Wojciechowski, M.F.; Lavin, M.; Sanderson, M.J. A phylogeny of legumes (Leguminosae) based on analysis of the plastid matK gene resolves many well-supported subclades within the family. Am. J. Bot. 2004, 91, 1846–1862. [Google Scholar] [CrossRef]
  23. Oyebanji, O.; Zhang, R.; Chen, S.Y.; Yi, T.S. New insights into the plastome evolution of the Millettioid/Phaseoloid clade (Papilionoideae, Leguminosae). Front. Plant Sci. 2020, 11, 151. [Google Scholar] [CrossRef] [PubMed]
  24. Vatanparast, M.; Powell, A.; Doyle, J.J.; Egan, A.N. Targeting legume loci: A comparison of three methods for target enrichment bait design in Leguminosae phylogenomics. Appl. Plant Sci. 2018, 6, e1036. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Egan, A.N.; Vatanparast, M.; Cagle, W. Parsing polyphyletic Pueraria: Delimiting distinct evolutionary lineages through phylogeny. Mol. Phylogenet. Evol. 2016, 104, 44–59. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Stefanović, S.; Pfeil, B.E.; Palmer, J.D.; Doyle, J.J. Relationships among phaseoloid legumes based on sequences from eight chloroplast regions. Syst. Bot. 2009, 34, 115–128. [Google Scholar] [CrossRef]
  27. De Queiroz, L.P.; Pastore, J.F.B.; Cardoso, D.; Snak, C.; Lima, A.L.d.C.; Gagnon, E.; Vatanparast, M.; Holland, A.E.; Egan, A.N.A. Multilocus phylogenetic analysis reveals the monophyly of a recircumscribed papilionoid legume tribe Diocleae with well-supported generic relationships. Mol. Phylogenet. Evol. 2015, 90, 1–19. [Google Scholar] [CrossRef]
  28. Edgar, R.C. MUSCLE: Multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res. 2004, 32, 1792–1797. [Google Scholar] [CrossRef] [Green Version]
  29. Hall, T.A. In BioEdit: A user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symp. Ser. 1999, 41, 95–98. [Google Scholar]
  30. Stamatakis, A. RAxML-VI-HPC: Maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models. Bioinformatics 2006, 22, 2688–2690. [Google Scholar] [CrossRef] [Green Version]
  31. Miller, M.A.; Pfeiffer, W.; Schwartz, T. Creating the CIPRES Science Gateway for inference of large phylogenetic trees. In Proceedings of the 2010 Gateway Computing Environments Workshop (GCE), New Orleans, LA, USA, 14 November 2010; pp. 1–8. [Google Scholar]
  32. Drummond, A.J.; Rambaut, A. BEAST: Bayesian evolutionary analysis by sampling trees. BMC Evol. Biol. 2007, 7, 214. [Google Scholar] [CrossRef] [Green Version]
  33. Lavin, M.; Herendeen, P.S.; Wojciechowski, M.F. Evolutionary rates analysis of Leguminosae implicates a rapid diversification of lineages during the tertiary. Syst. Biol. 2005, 54, 575–594. [Google Scholar] [CrossRef] [Green Version]
  34. Drummond, A.J.; Suchard, M.A.; Xie, D.; Rambaut, A. Bayesian phylogenetics with BEAUti and the BEAST 1.7. Mol. Biol. Evol. 2012, 29, 1969–1973. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  35. Maddison, W.P. Mesquite: A modular system for evolutionary analysis. Evolution 2008, 62, 1103–1118. [Google Scholar]
  36. Paradis, E.; Claude, J.; Strimmer, K.J.B. APE: Analyses of phylogenetics and evolution in R language. Bioinformatics 2004, 20, 289–290. [Google Scholar] [CrossRef] [PubMed]
  37. Harmon, L.J.; Weir, J.T.; Brock, C.D.; Glor, R.E.; Challenger, W. GEIGER: Investigating evolutionary radiations. Bioinformatics 2008, 24, 129–131. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  38. Nylander, J.A.; Olsson, U.; Alström, P.; Sanmartin, I. Accounting for phylogenetic uncertainty in biogeography: A Bayesian approach to dispersal-vicariance analysis of the thrushes (Aves: Turdus). Syst. Biol. 2008, 57, 257–268. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  39. Yu, Y.; Harris, A.; He, X. RASP (Reconstruct Ancestral State in Phylogenies) 1.1. Beta; Sichuan University: Sichuan, China, 2011. [Google Scholar]
  40. Zhisheng, A.; Kutzbach, J.E.; Prell, W.L.; Porter, S.C. Evolution of Asian monsoons and phased uplift of the Himalaya–Tibetan plateau since Late Miocene times. Nature 2001, 411, 62–66. [Google Scholar] [CrossRef]
  41. Che, J.; Zhou, W.W.; Hu, J.S.; Yan, F.; Papenfuss, T.J.; Wake, D.B.; Zhang, Y.P. Spiny frogs (Paini) illuminate the history of the Himalayan region and Southeast Asia. Proc. Natl. Acad. Sci. USA 2010, 107, 13765–13770. [Google Scholar] [CrossRef] [Green Version]
  42. Li, J.; Fang, X. Research on the uplift of the Qinghai-Xizang Plateau and environmental changes. Chin. Sci. Bull. 1998, 43, 1569–1574. [Google Scholar]
  43. Liu, X.; Dong, B. Influence of the Tibetan Plateau uplift on the Asian monsoon-arid environment evolution. Chin. Sci. Bull. 2013, 58, 4277–4291. [Google Scholar] [CrossRef] [Green Version]
  44. Shi, Y.; Li, J.; Li, B. Uplift of the Qinghai-Xizang (Tibetan) plateau and east Asia environmental change during late Cenozoic. Acta Geogr. Sin. 1999, 54, 20–28. [Google Scholar]
  45. Pokorny, L.; Riina, R.; Mairal, M.; Meseguer, A.S.; Culshaw, V.; Cendoya, J.; Serrano, M.; Carbajal, R.; Ortiz, S.; Heuertz, M. Living on the edge: Timing of Rand Flora disjunctions congruent with ongoing aridification in Africa. Front. Genet. 2015, 6, 154. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  46. Hoorn, C.; Wesselingh, F.P.; Ter Steege, H.; Bermudez, M.; Mora, A.; Sevink, J.; Sanmartín, I.; Sanchez-Meseguer, A.; Anderson, C.; Figueiredo, J. Amazonia through time: Andean uplift, climate change, landscape evolution, and biodiversity. Science 2010, 330, 927–931. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  47. Prothero, D.R. The late eocene-oligocene extinctions. Annu. Rev. Earth Planet Sci. 1994, 22, 145–165. [Google Scholar] [CrossRef]
  48. Crisp, M.D.; Cook, L.G. Explosive radiation or cryptic mass extinction? Interpreting signatures in molecular phylogenies. Evolution 2009, 63, 2257–2265. [Google Scholar] [CrossRef]
  49. Favre, A.; Michalak, I.; Chen, C.H.; Wang, J.C.; Pringle, J.S.; Matuszak, S.; Sun, H.; Yuan, Y.M.; Struwe, L.; Muellner-Riehl, A.N. Out of Tibet: The spatiotemporal evolution of Gentiana (Gentianaceae). J. Biogeogr. 2016, 43, 1967–1978. [Google Scholar] [CrossRef]
  50. Wen, J.; Zhang, J.Q.; Nie, Z.L.; Zhong, Y.; Sun, H. Evolutionary diversifications of plants on the Qinghai-Tibetan Plateau. Front. Genet. 2014, 5, 4. [Google Scholar] [CrossRef] [Green Version]
  51. Bagheri, A.; Maassoumi, A.A.; Rahiminejad, M.R.; Brassac, J.; Blattner, F.R. Molecular phylogeny and divergence times of Astragalus section Hymenostegis: An analysis of a rapidly diversifying species group in Fabaceae. Sci. Rep. 2017, 7, 14033. [Google Scholar] [CrossRef]
  52. Donkpegan, A.S.; Doucet, J.-L.; Hardy, O.J.; Heuertz, M.; Piñeiro, R. Miocene diversification in the Savannahs precedes tetraploid rainforest radiation in the african tree genus Afzelia (Detarioideae, Fabaceae). Front. Plant Sci. 2020, 11, 798. [Google Scholar] [CrossRef]
  53. Oliveira, L.C.; Rodrigues, D.P.; Hopkins, H.C.F.; Lewis, G.P.; Hopkins, M.J.G. Phylogeny and historical biogeography of the pantropical genus Parkia (Leguminosae, Caesalpinioideae, mimosoid clade). Mol. Phylogenet. Evol. 2021, 163, 107219. [Google Scholar] [CrossRef]
  54. Lu, H.; Wang, X.; Li, L. Aeolian sediment evidence that global cooling has driven late Cenozoic stepwise aridification in central Asia. Geol. Soc. Spec. Publ. 2010, 342, 29–44. [Google Scholar] [CrossRef]
  55. Miao, Y.; Herrmann, M.; Wu, F.; Yan, X.; Yang, S. What controlled Mid-Late Miocene long-term aridification in Central Asia? Global cooling or Tibetan Plateau uplift: A review. Earth Sci. Rev. 2012, 112, 155–172. [Google Scholar] [CrossRef]
  56. Mosbrugger, V.; Utescher, T.; Dilcher, D.L. Cenozoic continental climatic evolution of Central Europe. Proc. Natl. Acad. Sci. USA 2005, 102, 14964–14969. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  57. Graham, A. Late Cretaceous and Cenozoic History of Latin American Vegetation and Terrestrial Environments; Missouri Botanical Garden Press: St. Louis, MO, USA, 2010. [Google Scholar]
  58. Guo, Z.; Ruddiman, W.F.; Hao, Q.Z.; Wu, H.; Qiao, Y.; Zhu, R.X.; Peng, S.; Wei, J.; Yuan, B.; Liu, T. Onset of Asian desertification by 22 Myr ago inferred from loess deposits in China. Nature 2002, 416, 159–163. [Google Scholar] [CrossRef]
  59. Barbour, M.; Keeler-Wolf, T.; Schoenherr, A.A. Terrestrial Vegetation of California; University of California Press: Berkeley, CA, USA, 2007. [Google Scholar]
  60. Ramstein, G.; Fluteau, F.; Besse, J.; Joussaume, S. Effect of orogeny, plate motion and land-sea distribution on Eurasian climate change over the past 30 million years. Nature 1997, 386, 788–795. [Google Scholar] [CrossRef]
  61. Jacobs, B.F. Palaeobotanical studies from tropical Africa: Relevance to the evolution of forest, woodland and savannah biomes. Philos. Trans. R. Soc. Lond. B Biol. Sci. 2004, 359, 1573–1583. [Google Scholar] [CrossRef] [PubMed]
  62. De-Nova, J.A.; Medina, R.; Montero, J.C.; Weeks, A.; Rosell, J.A.; Olson, M.E.; Eguiarte, L.E.; Magallón, S. Insights into the historical construction of species-rich Mesoamerican seasonally dry tropical forests: The diversification of Bursera (Burseraceae, Sapindales). N. Phytol. 2012, 193, 276–287. [Google Scholar] [CrossRef]
  63. Töpel, M.; Antonelli, A.; Yesson, C.; Eriksen, B.; One, P. Past climate change and plant evolution in western North America: A case study in Rosaceae. PLoS ONE 2012, 7, e50358. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  64. Dodd, M.E.; Silvertown, J.; Chase, M.W. Phylogenetic analysis of trait evolution and species diversity variation among angiosperm families. Evolution 1999, 53, 732–744. [Google Scholar] [CrossRef]
  65. Eriksson, O.; Bremer, B. Pollination systems, dispersal modes, life forms, and diversification rates in angiosperm families. Evolution 1992, 46, 258–266. [Google Scholar] [CrossRef]
  66. Verdú, M. Age at maturity and diversification in woody angiosperms. Evolution 2002, 56, 1352–1361. [Google Scholar] [CrossRef]
  67. Pennington, R.T.; Lavin, M.; Prado, D.E.; Pendry, C.A.; Pell, S.K.; Butterworth, C.A. Historical climate change and speciation: Neotropical seasonally dry forest plants show patterns of both Tertiary and Quaternary diversification. Philos. Trans. R. Soc. Lond. B Biol. Sci. 2004, 359, 515–538. [Google Scholar] [CrossRef] [PubMed]
Genes 13 02220 g001 550
Figure 1. Combined chronogram and the summary of biogeographic analysis of the Millettiod legumes. Dating analysis was performed using BEAST software. The topology corresponds to the majority rule consensus tree of the Bayesian stationary sample. Large pie charts show the relative probabilities of alternative ancestral distributions obtained by statistical dispersal–vicariance analysis (white > red > blue > yellow); areas (frequencies < 0.1) are collectively given with black color.
Figure 1. Combined chronogram and the summary of biogeographic analysis of the Millettiod legumes. Dating analysis was performed using BEAST software. The topology corresponds to the majority rule consensus tree of the Bayesian stationary sample. Large pie charts show the relative probabilities of alternative ancestral distributions obtained by statistical dispersal–vicariance analysis (white > red > blue > yellow); areas (frequencies < 0.1) are collectively given with black color.
Genes 13 02220 g001
Genes 13 02220 g002 550
Figure 2. Habit shift analysis of the Millettiod legumes. Green represents herbaceous; red represents woody. Images are representative species from the Millettiod legumes.
Figure 2. Habit shift analysis of the Millettiod legumes. Green represents herbaceous; red represents woody. Images are representative species from the Millettiod legumes.
Genes 13 02220 g002
Genes 13 02220 g003 550
Figure 3. Biome evolutionary history of the Millettiod legumes. (A) World map of biome (edited from Lewis et al., 2005 [9]). (B) Ancestral biome state reconstruction of the Millettiod legumes using parsimony method.
Figure 3. Biome evolutionary history of the Millettiod legumes. (A) World map of biome (edited from Lewis et al., 2005 [9]). (B) Ancestral biome state reconstruction of the Millettiod legumes using parsimony method.
Genes 13 02220 g003
Genes 13 02220 g004 550
Figure 4. Lineage-through-time (LTT) plots of the Millettiod legumes. Dotted lines in red indicate the rapid increases in diversification rate.
Figure 4. Lineage-through-time (LTT) plots of the Millettiod legumes. Dotted lines in red indicate the rapid increases in diversification rate.
Genes 13 02220 g004
Table
Table 1. Results of diversification rate model-fitting test with parameters estimated under each model. “R” indicates the speciation rate, “St” indicates where the speciation rate shifts.
Table 1. Results of diversification rate model-fitting test with parameters estimated under each model. “R” indicates the speciation rate, “St” indicates where the speciation rate shifts.
ModelAICLikelihoodR1R2R3R4R5St1St2St3St4
pureBirth−1910.211956.10550.16607--------
bd−1928.547966.27350.10794--------
DDX−1930.799967.39940.05211--------
DDL−1908.208956.10410.16608--------
SPVAR−1926.028966.01420.24839--------
EXVAR−1926.544966.27180.23662--------
BOTHVAR−1924.329966.16440.24951--------
yule2rate−1929.337967.66860.166500.10857---0.04---
yule3rate−1932.285971.14230.071660.141140.19292--17.787.12--
yule4rate−1931.881972.94040.098260.289430.095920.19-11.5710.688.46-
yule5rate−1932.951975.47530.071660.133420.289430.095920.1917.7811.5710.688.46
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Jiang, D.; Liao, L.; Xing, H.; Chen, Z.; Luo, X.; Li, H.-L. Interplay of Ecological Opportunities and Functional Traits Drives the Evolution and Diversification of Millettiod Legumes (Fabaceae). Genes 2022, 13, 2220. https://doi.org/10.3390/genes13122220

AMA Style

Jiang D, Liao L, Xing H, Chen Z, Luo X, Li H-L. Interplay of Ecological Opportunities and Functional Traits Drives the Evolution and Diversification of Millettiod Legumes (Fabaceae). Genes. 2022; 13(12):2220. https://doi.org/10.3390/genes13122220

Chicago/Turabian Style

Jiang, Dongzhu, Linzheng Liao, Haitao Xing, Zhidan Chen, Xuemei Luo, and Hong-Lei Li. 2022. "Interplay of Ecological Opportunities and Functional Traits Drives the Evolution and Diversification of Millettiod Legumes (Fabaceae)" Genes 13, no. 12: 2220. https://doi.org/10.3390/genes13122220

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop