Int. J. Mol. Sci. 2012, 13(1), 71-83; doi:10.3390/ijms13010071

Article
Is Remusatia (Araceae) Monophyletic? Evidence from Three Plastid Regions
Rong Li 1,2, Tingshuang Yi 1,2 and Heng Li 1,*
1
Key Laboratory of Biodiversity and Biogeography, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China; E-Mails: lirong@mail.kib.ac.cn (R.L.); tingshuangyi@mail.kib.ac.cn (T.Y.)
2
Germplasm Bank of Wild Species in Southwest China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China
*
Author to whom correspondence should be addressed; E-Mail: liheng@mail.kib.ac.cn; Tel./Fax: +86-871-5223533.
Received: 18 November 2011; in revised form: 14 December 2011 / Accepted: 15 December 2011 /
Published: 22 December 2011

Abstract

: The genus Remusatia (Araceae) includes four species distributed in the tropical and subtropical Old World. The phylogeny of Remusatia was constructed using parsimony and Bayesian analyses of sequence data from three plastid regions (the rbcL gene, the trnL-trnF intergenic spacer, and the rps16 intron). Phylogenetic analyses of the concatenated plastid data suggested that the monophyly of Remusatia was not supported because R. hookeriana did not form a clade with the other three species R. vivipara, R. yunnanensis, and R. pumila. Nevertheless, the topology of the analysis constraining Remusatia to monophyly was congruent with the topology of the unconstrained analysis. The results confirmed the inclusion of the previously separate genus Gonatanthus within Remusatia and disagreed with the current infrageneric classification of the genus.
Keywords:
Araceae; phylogeny; Remusatia; taxonomy

1. Introduction

The herbaceous genus Remusatia Schott (Araceae) was established in 1832 and contains four species distributed in the tropical and subtropical Old World [14]. The species type Remusatia vivipara (Roxb.) Schott extends from Africa, Madagascar, southeastern Arabian Peninsula, and the Himalaya to southern China, and tropical Asia to Malesia, northern Australia, and the Pacific islands [2,4]. Remusatia hookeriana Schott and R. pumila (D. Don) H. Li and A. Hay are distributed in Nepal, Bhutan, Northeastern India, Southwestern China, and Northern Thailand [4]. Remusatia yunnanensis (H. Li and A. Hay) H. Li and A. Hay is endemic to Western Yunnan of China [4]. Species of Remusatia usually grow as epiphytes or lithophytes in a wide variety of habitats including forest, rocks and damp banks [1,2]. The tubers of Remusatia vivipara are used to treat mastitis, traumatic injuries, abscesses, and swellings [4].

Remusatia is characterized by a combination of characters including unbranched or branched stolons with numerous bulbils, peltate leaves, absent appendix at spadix, and entirely connate stamens [1,4]. Based on the position of the placenta, Li and Hay [5] divided Remusatia into two sections: sect. Remusatia and sect. Gonatanthus (Klotzsh) H. Li and A. Hay. Species of sect. Remusatia have parietal placenta and the inflorescence appearing before the leaf. This section includes Remusatia vivipara and R. hookeriana. Species of section Gonatanthus (Remusatia pumila and R. yunnanensis) have basal placenta and an inflorescence that appears with the leaf [5].

Historically, the group Gonatanthus was formally recognized as a separate genus with Gonatanthus pumilus (D. Don) Engler and Krause (=Remusatia pumila) as the type with basal placentation being the key difference [68]. However this difference was found to be inconsistent as placentation was observed to be either basal or parietal in species such as Remusatia hookeriana and Gonatanthus yunnanensis H. Li and A. Hay (=R. yunnanensis) [5]. As a result, the genus Gonatanthus was merged with Remusatia by Li and Hay [5]. Nevertheless, this classification needs to be further tested within a broader phylogenetic framework that includes many lineages from Araceae.

Previous molecular phylogenetic studies have only included a single species from Remusatia (R. vivipara). The most recent and comprehensive family-wide phylogenetic studies supported the placement of Remusatia in Colocasia clade or large Pistia clade based on coding (rbcL gene, matK gene) and non-coding (partial trnK intron, trnL intron, trnL-F spacer) plastid DNA sequences [9]. Remusatia has been suggested to be closely related to Ariopsis Nimmo, Steudnera K. Koch, and Colocasia Schott [911]. However, these previous studies focused on the relationships at tribal level and only sampled Remusatia vivipara. Species from section Gonatanthus have not been included. To gain a clearer understanding of the phylogenetic position of Remusatia, it is necessary to test its monophyly by including the remaining species.

In this study, we employ sequences of three coding or non-coding plastid regions (the rbcL gene, the trnL-trnF intergenic spacer, and the rps16 intron) to construct the phylogeny of Remusatia, because these sequences have been shown to be useful for inferring relationships at the generic and specific levels of Araceae [9,1117]. The objectives of this study are to (1) test the monophyly of Remusatia with all four species sampled, (2) confirm the combination of Gonatanthus with Remusatia, and (3) infer the phylogenetic relationships within the genus.

2. Results and Discussion

2.1. Results

We excluded the poly A or poly T, and the ambiguous alignment from the data sets (rps16, 25 bp between 195 and 219, 505 bp between 245 and 749, 29 bp between 791 and 819, and 6 bp between 1224 and 1229; trnL-F, 6 bp between 73 and 78, 4 bp between 126 and 129, 14 bp between 523 and 536, 211 bp between 696 and 906, 3 bp between 1096 and 1098, and 6 bp between 1102 and 1107). The aligned length, the numbers of variable and parsimony informative sites, and the best-fit model determined by Modeltest for each plastid region were given (Table 1). The variation among three regions is different and the rps16 intron is the most variable region. The single-gene analysis using maximum parsimony and Bayesian methods demonstrated no significant incongruences for the phylogeny of Remusatia among the three regions (Figure S1–S3). Moreover, a quantitative approach using the incongruence length difference (ILD) test also indicated no conflict among the three data sets (p = 0.04). We thus concatenated the three plastid data set in our analysis.

The aligned length, the numbers of variable sites, and the numbers of parsimony informative sites for the concatenated plastid regions were given (Table 1). Treating gaps as missing data, the maximum parsimony analysis produced 3 most parsimonious trees (MPTs) of 412 steps, with a consistency index (CI) of 0.83, a CI excluding uninformative characters of 0.71, a retention index (RI) of 0.84, and a rescaled consistency index (RC) of 0.70. The Bayesian tree was nearly identical to the strict consensus tree of MPTs (Figure 1). Treating the gaps as new characters, the parsimony strict consensus tree also did not support the monophyly of Remusatia (Figure S4). Moreover, the resulting tree when gaps were treated as missing data is better resolved than the tree obtained with gaps as coded characters. For this reason, we discuss all results in this paper based on the analysis treating gaps as missing data (Figure 1).

The concatenated plastid data supported the monophyly of the Colocasia clade (PB = 77%, PP = 1.0). Remusatia was part of the Colocasia clade (Figure 1). The monophyly of Remusatia was not supported because R. hookeriana did not form a clade with other three species R. vivipara, R. yunnanensis, and R. pumila (see Figure 1). Excluding Remusatia hookeriana, the remaining Remusatia species formed a supported clade (PB = 60%, PP = 0.97) (Figure 1). Within this clade, Remusatia pumila is sister to the clade containing R. vivipara and R. yunnanensis (Figure 1).

Analyses constraining all Remusatia species into a clade generated MPTs that were the same tree length with the unconstrained MPTs. The SH test suggests topological congruence is well supported (p > 0.01) between constrained analysis and unconstrained analysis (Figure S5).

2.2. Discussion

2.2.1. Is Remusatia Monophyletic?

With the current sampling, the monophyly of Remusatia is not supported. The species R. hookeriana does not group with the remainder of the Remusatia species sampled. However, the topology of the analysis constraining Remusatia to monophyly was congruent with the topology of unconstrained analysis (Figures 1 and S5). It is likely that the non-monophyly was due to the morphological and ploidy sampling bias, because our sampling for R. hookeriana remains poor (e.g., only three accessions having stolons branched and placentae parietal were sampled from R. hookeriana). Remusatia hookeriana is morphologically or cytologically variable in several characters including stolons simple or much branched, placentae parietal or basal, and chromosome numbers diploid or triploid [5,1822]. These characters are shared with the remaining Remusatia species. It seems likely that Remusatia hookeriana may be more closely related to the common ancestor of the remaining Remusatia species. Thus, the monophyly of Remusatia needs to be further examined with additional R. hookeriana sampling covered the morphological or cytological diversity.

It is difficult to establish any morphological synapomorphies for the Remusatia, because the defining characters except the unbranched or branched stolons also occur in other genera of Araceae. These include peltate leaves, appendix absent at spadix, entirely connate stamens, and chromosome base number x = 14 [1,4]. At the family level, many of these morphological or cytological characters including leaf shape, spadix structure, male flowers morphology, and chromosome number have been shown to be relatively plastic [1,9].

In our phylogenetic tree, the genus Remusatia and the genus Steudnera form a weakly supported clade (PB = 56%, PP < 0.95) (Figure 1), which share the characters of the appendix absent at the spadix and numerous ovules. They differ in that Steudnera has stout rhizomes and absent stolons, whereas Remusatia possesses subglobose tubers and produces erect or spreading, unbranched or branched stolons from the axils of deciduous cataphylls [1,4]. The rarely flowering Remusatia species are spread by the generous formation of tubercles from stolons [23].

2.2.2. Infrageneric Relationships Within Remusatia

Our phylogenetic analyses confirm the combination of previously separate genus Gonatanthus with Remusatia, because the G. pumilus (=R. pumila) (the type of Gonatanthus), G. yunnanensis (=R. yunnanensis), and R. vivipara (the type of Remusatia) formed a supported clade (Figure 1). Within this clade, Remusatia pumila is sister to the clade consisting of R. vivipara and R. yunnanensis (Figure 1). Morphologically, Remusatia pumila is distinguished from the other two species by not having a reflexed spathe with 2 constrictions (vs. reflexed spathe with only 1 constriction) [4,5]. Remusatia vivipara is phylogenetically close to R. yunnanensis, differing primarily in their stolon morphology and flowering time. Remusatia vivipara has erect, simple stolons and the inflorescence appearing before the leaf, whereas R. yunnanensis has creeping or pendulous, branched stolons and the inflorescence appearing together with the leaf [4,5].

In our study, the widely distributed Remusatia vivipara and narrowly endemic R. yunnanensis are represented by several accessions from Southern India and Yunnan in China. However, the monophyly of each species is not supported in the phylogenetic analyses. There may be several cryptic species in widespread Remusatia vivipara complex and in morphologically variable R. yunnanensis complex. Thus, a more thorough analysis (e.g., using genomic screening markers and additional taxon sampling) should be performed to confirm the status of Remusatia vivipara and R. yunnanensis.

Based on the placenta position, Li and Hay [5] split Remusatia into two sections: sect. Remusatia and sect. Gonatanthus (Klotzsh) H. Li and A. Hay. Our results do not support their infrageneric classification, because species with parietal or basal placentae do not form a clade. For example, Remusatia yunnanensis grouped with R. vivipara which has parietal placentae, rather than with R. pumila having basal placentae.

Below we provide a taxonomic key to the species of Remusatia to facilitate the identification of the four species [4]:

1a. Spathe with two constrictions, one separating tube and limb, one separating limb into two partsR. pumila
1b. Spathe with only one constriction separating tube and limb
 2a. Stonlons erect, simple, stoutR. vivipara
 2b. Stonlons creeping or pendulous, simple or branched, slender
  3a. Limb of spathe semispreading to erect, not reflexedR. hookeriana
  3b. Limb of spathe initially erect, later reflexedR. yunnanensis

3. Experimental Section

3.1. Taxon Sampling

Thirty accessions representing four species of Remusatia and 20 related taxa were included in this study (Table 2). Based on recent phylogenetic analyses of Araceae [9], the following genera were used as closely related taxa that represent major lineage within the large Pistia clade: Ariopsis, Steudnera, Colocasia, Alocasia (Schott) G. Don, Arisaema Martius, and Pinellia Tenore. Species of Pistia L. and Protarum Engl. were selected as outgroups because they have been shown to be outside the Colocasia clade within the large Pistia clade. The wide range of multiple taxa within the large Pistia clade was selected to further test the monophyly of Remusatia within a broader phylogenetic framework.

3.2. DNA Extractions, Amplification, and Sequencing

Total DNA was extracted from about 15 mg silica-gel dried leaf material using the DNeasy plant mini kits (QIAGEN, Mississauga, Ontario) following the manufacturer’s protocol or the modified CTAB extraction method [24].

Three coding or non-coding plastid regions (the rbcL gene, the trnL-trnF intergenic spacer, and the rps16 intron) markers were employed in this study. The following primers were used for both amplification and sequencing: “1F” and “1460R” for the rbcL gene [25], “c” and “f” for the single trnL-F region or as two fragments with “c + d” and “e + f” [26]; when this region could not be amplified successful using primer “c”, we used instead primer “c2” [27], “F” and “R2” for the rps16 intron [28]. Polymerase chain reaction (PCR) amplifications were performed in a 25 μL volume containing 1.5 mM MgCl2, 0.2 mM of each dNTP, 0.4 mM of each primer, 1 U of Taq polymerase (Bioline), and about 10–50 ng of DNA template under the following conditions: 3 min at 95 °C, followed by 37 cycles of 20 s at 94 °C, 30 s at 50 °C, and 40 s at 72 °C, and then a final 5 min extension at 72 °C.

The PCR products were purified using the polyethylene glycol (PEG) precipitation procedure following the protocol of Sambrook et al. [29]. Cycle sequencing was conducted using BigDye 3.1 reagents and carried out using the following profile: 35 cycles of 97 °C for 15 s, 50 °C for 5 s, and 60 °C for 4 min. The products of cycle-sequencing reactions were cleaned using the Sephadex columns (Amersham Pharmacia Biotech, Piscataway, New Jersey). The sequences were generated on an ABI prism 3730XL capillary sequencer (Applied Biosystems, Foster City, California). All sequences were newly generated in this study and have been deposited in GenBank (Table 2).

3.3. Sequence Alignment and Phylogenetic Analyses

The program Sequencher 4.5 (Gene Codes Corporation, Ann Arbor, Michigan) was used to evaluate chromatograms for base confirmation and to edit contiguous sequences. Sequences were initially aligned with ClustalX version 1.83 [30], followed by manual adjustments on Se-Al v2.0a11 [31].

To evaluate congruence of the three plastid (rbcL, trnL-F, rps16) data sets, we employed the partition homogeneity test or the incongruence length difference (ILD) test [32]. The partition homogeneity test was conducted with PAUP* version 4.0b10 [33] with 100 replicates, each with 100 random addition sequence replicates, tree bisection-reconnection (TBR) branch swapping, and keeping no more than 100 trees per random addition replicate. Following Cunningham [34], a significance level of p = 0.01 was adopted for this test.

Phylogenetic trees for each plastid region and the combined data set (concatenating the rbcL, trnL-F, and rps16) were constructed using maximum parsimony (MP) and Bayesian methods. The MP analyses was conducted using PAUP* version 4.0b10 [33]. All characters were weighted equally and gaps were treated as missing data and coded as binary characters for the concatenated plastid data set using the “simple gap coding” method [35]. The program GapCoder [36] was employed to score the insertions and deletions (indels). The most parsimonious trees were obtained with heuristic searches of 1000 replicates with random stepwise sequence addition, tree bisection-reconnection (TBR) branch swapping, collapse of zero-length branches, multiple tree option in effect, saving 100 trees from each random sequence addition. Parsimony bootstrap values (PB) for the clades [37] revealed in the most parsimonious trees (MPTs) were calculated with 500 bootstrap replicates. In each replicate, we performed 1000 random sequence addition replicates followed by tree bisection-reconnection (TBR) swapping, keeping no more than 10 trees per replicate. Tree statistics, including consistency index and the retention index, were calculated using PAUP*.

Modeltest 3.7 [38,39] was used to determine the optimal model of molecular evolution and gamma rate heterogeneity using the Akaike Information Criterion (AIC). Bayesian inference was implemented with MrBayes 3.1.2 [40] using a mixed model Bayesian analysis strategy. We assigned model parameters for each gene partition identified by AIC in Modeltest (Table 1). The Markov chain Monte Carlo (MCMC) algorithm was run for 10,000,000 generations with one cold and three heated chains, starting from random trees and sampling one out of every 1000 generations. Runs were repeated twice. The average standard deviation of split frequencies below 0.01 was examined to evaluate the convergence between the runs. The program Tracer 1.5 [41] was used to ensure that plots of the two analyses were converging on the same area and the log likelihoods had stabilized. The value of the effective sample size (ESS) for each statistic was above 200 after excluding the 25% burn-in. After discarding the trees saved prior to this point as burn-in, the remaining 7500 trees were used to construct majority-rule consensus trees using PAUP*. Nodes with posterior probabilities (PP) ≥ 0.95 in the consensus trees were considered statistically significant.

With Remusatia shown to be non-monophyletic in our initial analysis, we performed a constraint analysis using the concatenated plastid data set. With Remusatia constrained to be monophyletic, a parsimony analysis was performed with the heuristic search option using 1000 random sequence additions, TBR, and saving 100 trees from each random sequence addition. Shimodaira-Hasegawa (SH) test [42] was used to evaluate the topological congruence between gene trees produced by the likelihood method. The SH test was implemented in PAUP* with the best-fit model estimated using Modeltest 3.7 [38,39], RELL optimization, and 1000 bootstrap replicates to compare the difference between the RELL optimization and the computationally much more intensive full optimization. We compared the optimal trees (unconstrained) with constraint trees from the maximum likelihood analysis separately.

4. Conclusions

The present study constructed the first phylogeny of Remusatia. The monophyly of Remusatia was not supported by the concatenated plastid data (the rbcL gene, the trnL-trnF intergenic spacer, and the rps16 intron). Phylogenetic analyses confirmed the combination of previous separate genus Gonatanthus with Remusatia and disagreed with the current infrageneric classification of the genus.

Supplementary Materials

Acknowledgments

The study was supported by knowledge innovation engineering of the Chinese Academy of Sciences (2010KIBA06). Laboratory assistance was provided by Meiqing Yang and Yang Yang. We thank Yanmei Chen, Josef Bogner, and Pascal Bruggeman for collecting samples, Philip Thomas from the Royal Botanic Garden Edinburgh, and Peter Fritsch from California Academy of Sciences for revising an earlier version of this manuscript.

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Figure 1. The parsimony strict consensus tree of Remusatia based on concatenated plastid data, with gaps treated as missing data (tree length = 412 steps, CI = 0.83, RI = 0.84, and RC = 0.70). Parsimony bootstrap values (PB) for maximum parsimony analysis in 500 replicates > 50% are shown above the branches and Bayesian posterior probabilities (PP) ≥ 0.95 are indicated below the branches. Double dash shows that the PP value was lower than 0.95.

Click here to enlarge figure

Figure 1. The parsimony strict consensus tree of Remusatia based on concatenated plastid data, with gaps treated as missing data (tree length = 412 steps, CI = 0.83, RI = 0.84, and RC = 0.70). Parsimony bootstrap values (PB) for maximum parsimony analysis in 500 replicates > 50% are shown above the branches and Bayesian posterior probabilities (PP) ≥ 0.95 are indicated below the branches. Double dash shows that the PP value was lower than 0.95.
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Table 1. Characteristics of three plastid regions.

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Table 1. Characteristics of three plastid regions.
Aligned length (bp)Number of variable sites (%)Number of parsimony-informative sites (%)Model selected by AIC
rbcL gene122180 (6.6%)35 (2.9%)HKY + I + G
trnL-F intergenic spacer93685 (9.1%)45 (4.8%)TVM + G
rps16 intron1014160 (15.8%)73 (7.2%)TIM + G
Plastid concatenated3171325 (10.2%)153 (4.8%)
Table 2. Voucher information and GenBank accession numbers for Remusatia and related taxa used in this study. All collections are deposited at the Herbarium of Kunming Institute of Botany, Chinese Academy of Sciences (KUN).

Click here to display table

Table 2. Voucher information and GenBank accession numbers for Remusatia and related taxa used in this study. All collections are deposited at the Herbarium of Kunming Institute of Botany, Chinese Academy of Sciences (KUN).
TaxonVoucherLocalityGenBank Accession No.

rbcLtrnL-Frps16
Ingroups
Alocasia cucullata (Loureiro) G. DonR. Li 56China: Yunnan, XishuangbannaJQ237188JQ237218JQ237158
Alocasia odora (Roxburgh) K. KochR. Li 54China: Yunnan, XishuangbannaJQ237190JQ237220JQ237160
Ariopsis peltata NimmoH. AR 602S IndiaJQ237191JQ237221JQ237161
Ariopsis peltata Nimmos.n.S IndiaJQ237192JQ237222JQ237162
Arisaema bonatianum EnglerT.S. Yi 08006China: Yunnan, GongshanJQ237193JQ237223JQ237163
Arisaema elephas BuchetT.S. Yi 08008China: Yunnan, BaoshanJQ237194JQ237224JQ237164
Arisaema wattii J. D. HookerT.S. Yi 08011China: Yunnan, GongshanJQ237195JQ237225JQ237165
Colocasia antiquorum SchottT.S. Yi 08013China: Yunnan, TengchongJQ237199JQ237229JQ237169
Colocasia antiquorum SchottT.S. Yi 08014China: Yunnan, YingjiangJQ237200JQ237230JQ237170
Colocasia esculenta (L.) SchottR. Li 55China: Yunnan, Xishuangbanna, cultivatedJQ237189JQ237219JQ237159
Colocasia esculenta (L.) SchottR. Li 48China: Yunnan, Lvchun, cultivatedJQ237196JQ237226JQ237166
Colocasia gigantea (Blume) J. D. HookerR. Li 66China: Yunnan, LvchunJQ237197JQ237227JQ237167
Colocasia gigantea (Blume) J. D. HookerR. Li 69China: Yunnan, JinpingJQ237198JQ237228JQ237168
Pinellia cordata N. E. BrownT.S. Yi 08015China: Fujian, WuyishanJQ237201JQ237231JQ237171
Pinellia peltata C. PeiT.S. Yi 08016China: Zhejiang, WenzhouJQ237202JQ237232JQ237172
Ingroups
Pinellia ternata (Thunb.) Tenore ex BreitenbachT.S. Yi 08018China: Yunnan, KunmingJQ237203JQ237233JQ237173
Remusatia hookeriana SchottY.M. Chen 26China: Yunnan, WudingJQ237206JQ237236JQ237176
Remusatia hookeriana SchottR. Li 10China: Yunnan, JinpingJQ237207JQ237237JQ237177
Remusatia hookeriana SchottR. Li 46China: Yunnan, LvchunJQ237208JQ237238JQ237178
Remusatia pumila (D. Don) H. Li & A. HayR. Li 13China: Yunnan, PingbianJQ237209JQ237239JQ237179
Remusatia pumila (D. Don) H. Li & A. HayR. Li 43China: Yunnan, LvchunJQ237210JQ237240JQ237180
Remusatia vivipara (Roxb.) SchottR. Li 12China: Yunnan, JinpingJQ237211JQ237241JQ237181
Remusatia vivipara (Roxb.) SchottR. Li 44China: Yunnan, LvchunJQ237212JQ237242JQ237182
Remusatia vivipara (Roxb.) Schotts.n.S IndiaJQ237213JQ237243JQ237183
Remusatia yunnanensis (H. Li & A. Hay) H. Li & A. HayR. Li 11China: Yunnan, YingjiangJQ237214JQ237244JQ237184
Remusatia yunnanensis (H. Li & A. Hay) H. Li & A. HayR. Li 45China: Yunnan, YingjiangJQ237215JQ237245JQ237185
Steudnera colocasiifolia K. KochR. Li 14China: Yunnan, PuerJQ237216JQ237246JQ237186
Steudnera colocasiifolia K. KochR. Li 51China: Yunnan, XishuangbannaJQ237217JQ237247JQ237187
Outgroups
Pistia stratiotes L.T.S. Yi 08020China: Yunnan, KunmingJQ237204JQ237234JQ237174
Protarum sechellarum Engl.Bogner s.n.Germany: Munich Botanical Garden, cultivatedJQ237205JQ237235JQ237175
Int. J. Mol. Sci. EISSN 1422-0067 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert