New insights into intergeneric relationships of Hickeliinae (Poaceae: Bambusoideae) revealed by complete plastid genomes

Abstract

The Hickeliinae (Poaceae: Bambusoideae) is an ecologically and economically significant subtribe of tropical bamboos restricted to Madagascar, Comoros, Reunion Island, and a small part of continental Africa (Tanzania). Because these bamboos rarely flower, field identification is challenging, and inferring the evolutionary history of Hickeliinae from herbarium specimens is even more so. Molecular phylogenetic work is critical to understanding this group of bamboos. Here, comparative analysis of 22 newly sequenced plastid genomes showed that members of all genera of Hickeliinae share evolutionarily conserved plastome structures. We also determined that Hickeliinae plastome sequences are informative for phylogenetic reconstructions. Phylogenetic analysis showed that all genera of Hickeliinae are monophyletic, except for Nastus, which is paraphyletic and forms two distant clades. The type species of Nastus (Clade II) is endemic to Reunion Island and is not closely related to other sampled species of Nastus endemic to Madagascar (Clade VI). Clade VI (Malagasy Nastus) is sister to the Sokinochloa + Hitchcockella clade (Clade V), and both clades have a clumping habit with short-necked pachymorph rhizomes. The monotypic Decaryochloa is remarkable in having the longest floret in Bambuseae and forms a distinct Clade IV. Clade III, which has the highest generic diversity, consists of Cathariostachys, Perrierbambus, Sirochloa, and Valiha, which are also morphologically diverse. This work provides significant resources for further genetic and phylogenomic studies of Hickeliinae, an understudied subtribe of bamboo.

Highlights

• •Hickeliinae is a Bambusoideae subtribe endemic to Madagascar, Comoros, La Reunion and Tanzania.
• •Our study provides a comprehensive understanding of Hickeliinae phylogeny at the generic level based on plastome data.
• •Molecular phylogeny indicates that all genera of Hickeliinae are monophyletic except for Nastus Juss.

1. Introduction

The Bambusoideae (bamboos) is one of 12 currently recognized subfamilies of the Poaceae (grasses) unambiguously supported by recent analyses (Bouchenak-Khelladi et al., 2008; GPWG II 2012; Wu and Ge, 2012; Saarela et al., 2018). Bamboos, which naturally occur on all continents except Europe and Antarctica (Li, 1998; Ohrnberger, 1999; Bamboo Phylogeny Group et al., 2012; Soreng et al., 2022), currently total 1642 species in 115 genera (Vorontsova et al., 2016), although these numbers continue to change with new combinations and discoveries (e.g., Haevermans et al., 2020; Tong et al., 2020; Zhang et al., 2020; Ruiz-Sanchez et al., 2021; Ye et al., 2021b). Three tribes, i.e., Arundinarieae (temperate woody bamboos), Bambuseae (tropical woody bamboos) and Olyreae (herbaceous bamboos), are widely recognized. The tribe Bambuseae is further divided into the paleotropical woody bamboos and the neotropical woody bamboos (Sungkaew et al., 2009; Triplett et al., 2014; Kellogg, 2015; Saarela et al., 2018; Guo et al., 2019). The paleotropical woody bamboos have, in turn, been divided into eight subtribes, one of which is named the Hickeliinae A. Camus (Camus, 1924; Dransfield 1994, 1997, 1998, 2000, 2002, 2003, 2016).

All native woody bamboo species of Madagascar fall into two subtribes, the Hickeliinae (Bambuseae) and the Thamnocalaminae (Arundinarieae) (Zhou et al., 2017; Zhang et al., 2017, 2020), except for Schizostachyum perrieri A. Camus (Vorontsova et al., 2016). However, Schizostachyum Nees is a genus of the Melocalanninae distributed in Southeast Asia, extending to New Guinea, Melanesia and Polynesia. The identity of S. perrieri is questionable (Zhou et al., 2022) and probably belongs to Oldeania Stapleton judging from the type specimen deposited at the Muséum National d’Histoire Naturelle. Dransfield (2000) inferred that it may be conspecific with Arundinaria madagascariensis A. Camus which has been transferred into Oldeania (Zhang et al., 2017). After transferring 11 Malesian species of Nastus Juss. to Chloothamnus Buse (subtribe Racemobambosinae Stapleton), Ruhooglandia S. Dransf. & K.M. Wong (subtribal position uncertain) and Widjajachloa K.M. Wong & S. Dransf. (subtribe Racemobambosinae) (Widjaja and Wong, 2016; Wong and Dransfield, 2016), Hickeliinae currently includes 9 genera and 32 species: Cathariostachys S. Dransf. (2 spp.), Decaryochloa A. Camus (1 sp.), Hickelia A. Camus (4 spp.), Hitchcockella A. Camus (1 sp.), Nastus (12 spp.), Perrierbambus A. Camus (2 spp.), Sirochloa S. Dransf. (1 sp.), Sokinochloa S. Dransf. (7 spp.), and Valiha S. Dransf. (2 spp.) (Dransfield, 2016; Vorontsova et al., 2016). The heterogeneity and revision of Nastus s.l. have also been revealed and supported by plastid phylogeny (Chokthaweepanich, 2014; Zhou et al., 2017). All Hickeliinae species, except Nastus borbonicus J. F. Gmel. (Reunion Island) and Hickelia africana S. Dransf. (Tanzania), are endemic to Madagascar, with Sirochloa parvifolia S. Dransf. extending to Comoros. The majority of species in the Hickeliinae are found on the eastern escarpment, where remnants of wet rainforest still exist and a variety of ecological niches are found. Hickelia is found in montane forests (Dransfield, 1994), whereas Sirochloa and Valiha are found in coastal areas at lower elevations (Dransfield, 1998, 2002). Perrierbambus grows in the drier vegetation in the west of Madagascar (Vorontsova et al., 2018). Nastus, the largest genus, is abundant in forested areas and forest margins (Dransfield, 2003). Sokinochloa, which is the most recently described and revised genus, is also found across Madagascar’s forests and their margins (Dransfield, 2016). Madagascar’s fauna, particularly lemurs, and its people depend on these bamboos (Dransfield, 2003; King et al., 2013). Despite the common occurrence of Hickeliinae species and their close relationships with economically significant invasive and edible species (Canavan et al., 2016), the phylogenetic relationships among Hickeliinae genera are poorly understood.

Diagnostic morphological characters of subtribe Hickeliinae include an erect culm in the lower part with a scrambling or climbing upper part, nodes that dip downward with an extravaginal branch, determinate inflorescence (spike or capitate) with one floret in the spikelet, and pachymorph rhizomes (Vorontsova et al., 2018). Woody bamboos are famous for their rare and often unpredictable flowering (Janzen, 1976; Li et al., 2006; Ma et al., 2017), and the Hickeliinae is no exception (Dransfield, 2000). Consequently, collecting flowering material for identification and classification is challenging. Molecular data and plastome sequences, in particular, have provided invaluable information for resolving the phylogenetic relationships of bamboos and grasses (Zhou et al., 2017; Saarela et al., 2018). However, molecular approaches have yet to clarify phylogenetic relationships in Hickeliinae. Although one study used five chloroplast markers to confirm the monophyly of the subtribe, these markers lacked sufficient informative sites to resolve phylogenetic relationships among genera (Hackel et al., 2018). One potential approach to resolving complex evolutionary relationships such as those in the subtribe Hickeliinae is the use of comparative plastome analysis (Shaw et al., 2007; Moore et al., 2010; Park et al., 2017; Li et al., 2021). Plastomes, which have a circular quadripartite structure containing a large single-copy (LSC) region and a small single-copy (SSC) region separated by two inverted repeats (IRs) (Palmer, 1991), show a relatively high degree of conservatism in size, structure, and gene content across land plants (Wicke et al., 2011). In the past ten years, plastid phylogenomic analyses have been used to address evolutionary questions and have been widely applied in the Bambusoideae to resolve relationships at the subfamilial, tribal, and subtribal levels (Zhang et al., 2011; Wu and Ge, 2012; Ma et al., 2014; Wysocki et al., 2015; Ye et al., 2021a).

Here, we used genome skimming to acquire whole plastid genomes of 22 representative species of the subtribe Hickeliinae. Our aim was to (1) determine whether Hickeliinae plastome sequences are structurally similar to those of other Bambusoideae; (2) assess whether plastome sequences are sufficiently informative to resolve evolutionary relationships within this subtribe; (3) confirm whether Hickeliinae genera are monophyletic. We hope to contribute to a valuable phylogenetic framework for future taxonomic and ecological studies of bamboos in Madagascar.

2. Materials and methods

2.1. Plant material and taxon sampling

We sampled 22 species, covering all genera and about 69% of the known species of Hickeliinae. All species sampled here are endemic to Malagasy except Nastus borbonicus (from Reunion Island) and Hickelia africana (from Tanzania). The samples included in this study were collected during targeted field trips in Madagascar in 2017 and 2018. Fresh leaves and other plant materials were collected from the eastern humid forest (Andasibe and Maromizaha) and northeastern mountains (Marojejy) to the western drier areas (Ambanja) of Madagascar. These localities were chosen because of previous collections of the Hickeliinae and their rich biodiversity. During the field survey, we collected flowering material of three bamboo species: Hickelia perrieri (A. Camus) S. Dransf., Nastus tsaratananensis A. Camus and Nastus perrieri A. Camus. This material represents the first modern collection of native flowering bamboos from the montane forest bamboo diversity hotpot on Madagascar’s highest mountain, Tsaratanana. Fresh leaves were silica-gel-dried and stored for DNA extraction. Voucher specimens were deposited at herbaria in Parc Botanique et Zoologique de Tsimbazaza (TAN), Kunming Institute of Botany, Chinese Academy of Sciences (KUN), Royal Botanic Gardens, Kew (K), and Muséum National d'Histoire Naturelle (P). Some experimental materials were sampled from specimens deposited at K and P. Data on collection provenance and voucher specimens are shown in Table 1.

Table 1.

Voucher information and provenance of species sampled in this study. An additional reference sequence originally assembled by Wysocki et al. (2015) was also included: KJ870994, based on Dransfield 1349 collected from Ambatofitorahana in Madagascar.

Species	Country of origin	Silica gel or herbarium specimens used (S/H)	Voucher	Accession number
Hickelia madagascariensis (reference)	Madagascar	H	S. Dransfield 1349	KJ870994
Cathariostachys capitata	Madagascar	H	S. Dransfield 1064	GWHBHNA01000000
C. madagascariensis	Madagascar	S	R. A. Rakotonasolo 015	GWHBHMZ01000000
Decaryochloa diadelpha	Madagascar	S	R. A. Rakotonasolo 016	GWHBHMY01000000
Hickelia africana	Tanzania	H	S. Bidgood 221	GWHBHMX01000000
H. madagascariensis	Madagascar	H	S. Dransfield 1290	GWHBHMW01000000
H. perrieri	Madagascar	H	R. A. Rakotonasolo 071	GWHBHMV01000000
Hitchcockella baronii	Madagascar	H	D. Ravelonarivo & T. Augustin 3430	GWHBHMU01000000
Nastus aristatus	Madagascar	S	R. A. Rakotonasolo 022	GWHBHMT01000000
N. borbonicus	Reunion Island	S	T. Hubert s.n.	GWHBHMS01000000
N. elongatus	Madagascar	S	R. A. Rakotonasolo 024	GWHBHMR01000000
N. emirnensis	Madagascar	H	S. Dransfield 1119	GWHBHMQ01000000
N. humbertianus	Madagascar	H	H. Humbert 13668	GWHBHMP01000000
N. perrieri	Madagascar	S	R. A. Rakotonasolo 032	GWHBHMO01000000
N. tsaratananensis	Madagascar	S	H. Perrier 16170	GWHBHMN01000000
Perrierbambus madagascariensis	Madagascar	H	L. Nusbaumer 1954	GWHBHMM01000000
Sirochloa parvifolia	Madagascar	S	M. S. Vorontsova 1769	GWHBHML01000000
Sokinochloa australis	Madagascar	H	S. Dransfield 1506	GWHBHMK01000000
S. brachyclada	Madagascar	S	R. A. Rakotonasolo 028	GWHBHMJ01000000
S. chapelieri	Madagascar	H	D. K. Edelman 152	GWHBHMI01000000
S. chiataniae	Madagascar	H	Chia Tan 099	GWHBHMH01000000
S. viguieri	Madagascar	H	J. Dransfield 7749	GWHBHMG01000000
Valiha diffusa	Madagascar	H	R. A. Rakotonasolo 014	GWHBHMF01000000

2.2. DNA extraction and sequencing

Genomic DNA was extracted from leaf tissue and isolated using the TIANGEN DNAsecure Plant Kit following the manufacturer’s instructions, or from herbarium specimens following Zeng et al. (2018). The Illumina Hiseq platform was used to sequence paired-end reads. Library preparation and sequencing were carried out at the Laboratory of Molecular Biology, the Germplasm Bank of Wild Species (Kunming, China) and BGI Genomics Co., Ltd. (Shenzhen, China).

2.3. Plastid genome assembly and annotation

Plastid genomes were assembled using the GetOrganelle toolkit (Jin et al., 2020). We used Bandage v.8.0 (Wick et al., 2015) to visualize newly assembled plastome structure. Hickelia madagascariensis A. Camus was retrieved from GenBank (accession number: KJ_870994) and used as the reference plastome (Wysocki et al., 2015). Annotation was conducted in Geneious v.9.1.4 using MAFFT (Kearse et al., 2012) to align plastome sequences; annotations were transferred from the reference plastome. MAFFT was also used to align all plastomes. Annotations and alignments were checked manually. Gene maps of circular complete plastomes were drawn using OGDRAW (Lohse et al., 2013). Geneious v.9.1.4 was used to inspect the boundaries between LSC, IRa, SSC, IRb and the GC content for each species. Whole plastid sequence data have been deposited in the Genome Warehouse in National Genomics Data Center, Beijing Institute of Genomics, Chinese Academy of Sciences/China National Center for Bioinformation, which are publicly accessible at https://ngdc.cncb.ac.cn/gwh.

2.4. Comparative genomic and phylogenetic analysis

Using Hickelia madagascariensis (KJ_870994) as a reference, we compared the plastomes of the species sampled in this study. The assembled plastomes of Hickeliinae were aligned and plotted using the mVista program with LAGAN mode (Frazer et al., 2004). The rearrangement analysis of all plastomes was performed using Mauve alignment with default values for all parameters (Darling et al., 2004). The borders between LSC, IRa, SSC and IRb were investigated using IRscope (Amiryousefi et al., 2018).

To determine the phylogenetic relationships of the species sampled and test the support for the relationships within the subtribe, maximum likelihood (ML) was used to reconstruct a phylogenetic tree using whole plastome sequences of all sampled species in RAxML v.8.2.10 with the GTR + G + I model and 1000 rapid bootstrap replicates (Stamatakis, 2014). Bayesian inference (BI) was carried out in MrBayes v.3.2.6 (Ronquist et al., 2012). Markov chain Monte Carlo (MCMC) chains were run for 2 × 10,000,000 generations. Both analyses were performed on CIPRES Science Gateway (Miller et al., 2010). To root the tree, three species of Bambusa Schreb. were retrieved from GenBank and used as outgroup taxa (B. teres Buch.-Ham. ex Munro: NC_050751.1, B. oliveriana Gamble: MK679792.1 and B. vulgaris Schrad. ex J.C.Wendl: NC_050780.1).

3. Results

3.1. Plastome organizations and features in the subtribe Hickeliinae

The plastomes of all species showed a typical quadripartite structure (Fig. 1). Data on plastome size, length, and GC content of LSC, SSC and IR are shown in Table 2. All plastomes shared a common structure, consisting of two IR (21,773–21,804 bp) regions separated by an LSC (81,925–83,018 bp) region and an SSC (12,485–12,863 bp) region. The SSC region had the lowest GC content (33.1%–33.4%) followed by the LSC region (36.9%–37%), while that of the IR regions (44.2%) was constant and the highest. All plastomes contained the same 128 genes. A total of 110 unique genes were found, and 18 genes were duplicated in the IR regions (Table 3). The 110 unique genes comprise 77 protein-coding genes, 29 tRNA genes and 4 rRNA genes.

Fig. 1.

Plastome map of Valiha diffusa. Genes inside the circle are transcribed clockwise; genes outside the circle are transcribed counter-clockwise. The light gray inner circle corresponds to AT content, and the dark gray to GC content. Genes belonging to different functional groups are shown in different colors.

Table 2.

Structure of the plastomes analyzed in this study.

Taxon name	Plastome genome size (bp)	LSC length (bp)	GC content of LSC (%)	IR length (bp)	GC content of IR (%)	SSC length (bp)	GC content of SSC (%)
Hickelia madagascariensis (reference)	138,276	81,925	37	21,804	44.2	12,743	33.1
Cathariostachys capitata	138,606	82,550	36.9	21,782	44.2	12,492	33.3
C. madagascariensis	138,462	82,425	37	21,776	44.2	12,485	33.3
Decaryochloa diadelpha	139,073	82,762	37	21,782	44.2	12,747	33.2
Hickelia africana	138,290	81,966	37	21,790	44.2	12,744	33.1
H. madagascariensis	138,284	81,936	37	21,803	44.2	12,742	33.1
H. perrieri	138,250	81,941	37	21,788	44.2	12,733	33.2
Hitchcockella baronii	139,167	82,779	36.9	21,786	44.2	12,616	33.1
Nastus aristatus	139,380	82,961	37	21,778	44.2	12,863	33.1
N. borbonicus	138,953	82,619	36.9	21,787	44.2	12,760	33.2
N. elongatus	139,287	82,973	37	21,775	44.2	12,764	33.2
N. emirnensis	139,291	82,962	37	21,774	44.2	12,781	33.2
N. humbertianus	139,291	82,962	37	21,774	44.2	12,781	33.2
N. perrieri	139,328	82,946	37	21,776	44.2	12,830	33.3
N. tsaratananensis	139,272	82,950	37	21,774	44.2	12,774	33.3
Perrierbambus madagascariensis	139,134	82,827	36.9	21,786	44.2	12,735	33.1
Sirochloa parvifolia	139,346	83,018	36.9	21,782	44.2	12,764	33.1
Sokinochloa australis	138,258	81,958	37	21,773	44.2	12,754	33.3
S. brachyclada	138,286	82,001	37	21,779	44.2	12,727	33.3
S. chapelieri	139,149	82,847	37	21,782	44.2	12,738	33.2
S. chiataniae	139,045	82,749	37	21,781	44.2	12,734	33.3
S. viguieri	139,147	82,801	37	21,782	44.2	12,782	33.2
Valiha diffusa	138,937	82,862	37	21,775	44.2	12,525	33.4

Table 3.

Gene content in the Hickeliinae plastomes.

Category	Group of gene	Name of gene
Self-replication	Ribosomal RNA genes	rrn4.5a	rrn5a	rrn16a	rrn23a
	Transfer RNA genes	trnA-UGCa	trnC-GCA	trnD-GUC	trnE-UUC
		trnF-GAA	trnfM-CAU∗	trnG-UCC	trnH-CAU
		trnH-GUGa	trnI-GAUa	trnK-UUU	trnL-CAA
		trnL-UAA	trnL-UAG	trnN-GUUa	trnP-UGG
		trnQ-UUG	trnR-ACGa	trnR-UCU	trnS-GCU
		trnS-GGA	trnS-UGA	trnT-GGU	trnT-UGU
		trnV-GACa	trnV-UAC	trnW-CCA	trnY-GUA
	Small subunit of ribosome	rps2	rps3	rps4	rps7a
		rps8	rps11	rps12a,b	rps14
		rps15a	rps16	rps18	rps19a
	Large subunit of ribosome	rpl2a	rpl14	rpl16	rpl20
		rpl22	rpl23a	rpl32	rpl33
		rpl36
	RNA polymerase subunit	rpoA	rpoB	rpoC1	rpoC2
Photosynthesis	Subunits of photosystem I	psaA	psaB	psaC	psaI
		psaJ
	Subunits of photosystem II	psbA	psbB	psbC	psbD
		psbE	psbF	psbH	psbI
		psbJ	psbK	psbL	psbM
		psbN	psbT	psbZ
	Subunits of cytochrome	petA	petB	petD	petG
		petL	petN
	Subunits of ATP synthetase	atpA	atpB	atpE	atpF
		atpH	atpI
	Large subunit of rubisco	rbcL
	Subunits of NADH	ndhA	ndhBa	ndhC	ndhD
		ndhE	ndhF	ndhG	ndhHa
		ndhI	ndhJ	ndhK
Other gene	Translation initiation factor	infA
	Maturase	matK
	Envelope membrane protein	cemA
	C-type cytochrome synthesis gene	ccsA
	Protease	clpP
Unknown function	Conserved open reading frames	ycf3		ycf4

^aTwo gene copies in IRs.

^bGene divided into two independent transcription units.

^∗Gene containing one intron.

3.2. Structural variations of the plastome

The structure of all plastomes in this study was relatively conserved, except for in the trnG-trnT region (Fig. S1). Plastome size ranged from 138,250 bp (Hickelia perrieri) to 139,380 bp (Nastus aristatus A. Camus). Although gene organization did not show evidence of rearrangement from the examination with Mauve (Fig. S2), the length of three plastome regions varied between species. In addition, the LSC and SSC regions were less conserved than the IR region. We also noted variations at the four boundaries between the single-copy region and the IR region shown by the results of IRscope (Fig. S3). ndhH was the only gene that spans the junction of the single-copy region and IR region in all species. ndhF exclusively spans the JSA junction of Sokinochloa viguieri (A. Camus) S. Dransf. and Nastus aristatus.

3.3. Plastid phylogenomic analyses

Our analyses showed that the subtribe Hickeliinae consists of six clades. The topologies reconstructed by BI and ML analyses were largely congruent (Fig. 2). The topologies from the BI and ML analyses were either the same, or ML analyses yielded less resolved or less supported trees than BI analysis. Analyses of complete plastome data resolved the phylogenetic relationships within Hickeliinae with high statistical support on most nodes (MLBS >90, PP = 1.00). In our tree, Nastus borbonicus from Reunion Island is sister to Hickelia with relatively low bootstrap support. The tree is compatible with a basal trichotomy for the three main clades: Clade II/Clade I/and Clade III + IV + V + VI.

Fig. 2.

ML tree based on whole plastome sequences using three species of Bambusa as outgroup taxa. Numbers near nodes indicate maximum likelihood bootstrap (MLBS)/Bayesian inference posterior probability (PP). Species names in bold are types of genera.

Major clades are well supported with strong statistical support (Fig. 2). Clade I consists of all sampled species of Hickelia (H. africana, H. perrieri and H. madagascariensis). Clade II contains only one species, Nastus borbonicus, which is endemic to Reunion Island. Clade III consists of five species from three oligotypic genera and one monotypic genus, i.e., Perrierbambus madagascariensis A. Camus, Sirochloa parvifolia, Valiha diffusa S. Dransf., Cathariostachys madagascariensis (A. Camus) S. Dransf. and Cathariostachys capitata (Kunth) S. Dransf. Clade IV consists of the monotypic genus Decaryochloa. Clade V consists of Sokinochloa and the monotypic Hitchcockella. Clade VI consists of Malagasy species of Nastus (N. aristatus, N. elongatus A. Camus, N. emirnensis A. Camus, N. perrieri, N. humbertianus A. Camus and N. tsaratananensis). All sampled Malagasy species of Nastus (Clade VI) are in another clade of the Hickeliinae with strong bootstrap support, whereas Nastus borbonicus from Reunion Island forms a basal clade of Hickeliinae sister to Hickelia with high posterior probability and low bootstrap support.

4. Discussion

The accessibility of plant plastome sequences has increased swiftly over the last decade. However, plastome data from species of Hickeliinae has remained scarce. We present here the most comprehensively sampled data set of plastid genomes and an explicit phylogeny for the neglected bamboo subtribe Hickeliinae. In total, 22 plastome sequences were newly generated covering all recognized genera of Hickeliinae.

4.1. Plastome structure is conserved in Hickeliinae and similar to that of other Bambusoideae subtribes

The structure and length of all the plastomes analyzed in our study are conserved. The plastome structures, gene contents and gene orders of Hickeliinae are consistent with that of other bamboo species (Zhang et al., 2011; Ma et al., 2014; Wysocki et al., 2015). These similarities indicate that the plastome structure of Hickeliinae is largely conserved following patterns across the Bambusoideae.

4.2. Monophyly of the Hickeliinae and phylogenetic relationships among main clades

Our phylogenetic analysis based on plastome data confirmed that, except for Nastus, all currently-recognized genera of Hickeliinae are monophyletic. These genera had previously been delimited based on morphology. In our phylogenetic tree, Clade II consists of Nastus borbonicus, which is the type species and only species of Nastus distributed outside Madagascar. Morphologically, Nastus borbonicus is characterized by its erect culms and pachymorph rhizomes with long necks (Dransfield, 2000; Bosser and Renvoize, 2018).

Clade I consists of species of Hickelia, which was previously suggested as an early diverged genus in Hickeliinae (Chokthaweepanich, 2014; Zhou et al., 2017; Hackel et al., 2018). Hickelia is found in Malagasy dry highland forests with one species in wet montane forests of Tanzania (Dransfield, 1994). The culm of it is erect at the base and then scrambles over nearby vegetation at the upper part (Dransfield, 1994). Based on the order of divergence in Clade II, Hickelia is most likely native to Madagascar and subsequently dispersed to Africa.

Clade III is highly heterogeneous, including four genera (i.e., Cathariostachys, Perrierbambus, Sirochloa, and Valiha) of plants characterized by having culms that are erect on the lower part. Plants of these four genera grow at low to mid-elevations, distributed from montane forests to relatively drier coastal forests. Sirochloa has an open clumping habit, whereas the other three genera grow scattered. The culms of Perrierbambus and Sirochloa are solid, whereas those of the other two are hollow. The inflorescence types are capitate, paniculate, spicate, and racemose in Cathariostachys, Perrierbambus, Sirochloa, and Valiha, respectively (Dransfield, 1998, 2000, 2002, 2003).

Members of Clades IV–VI are wet forest climbers that grow in mid-elevation habitats (Dransfield, 1997, 2016; Vorontsova et al., 2018). The monotypic genus Decaryochloa (Clade IV), which is remarkable in having the longest floret in tropical woody bamboos (Bambuseae), is sister to Clades V and VI, the most speciose clades. The climbing bamboos of Malagasy Nastus (Clade VI) and Sokinochloa (Clade V) have the highest species diversity in the subtribe (Dransfield, 2016). Species in these two clades are similar in having pachymorph rhizomes with short necks that lead to their clumping habit. However, the capitate inflorescence of Sokinochloa is significantly different from that of the other two genera, which are paniculate or racemose. The wet forest climber Hitchcokella is one of the rarest and most enigmatic members of the Hickeliinae and is much in need of further study (Vorontsova et al., 2018).

Our work shows that plastome sequences are sufficiently informative to resolve the phylogeny of Hickeliinae. In addition, our Hickeliinae phylogeny is the most explicit and robust framework to date for this bamboo subtribe. Our phylogeny updates the most recent study involving Hickeliinae, which included a sampling of 15 species from all genera of Hickeliinae and used 5 plastid markers to infer phylogeny (Hackel et al., 2018). Our analyses shared two samples with theirs: One is the plastome sequence of Hickelia madagascariensis (Dransfield 1349 from Ambatofitorahana in Madagascar) previously sequenced by Wysocki et al. (2015) and used here as the reference sequence. Another is a herbarium sample of the rare species Hitchcockella baronii A. Camus (Ravelonarivo and Augustin 3430 from Marojejy in Madagascar, http://legacy.tropicos.org/Specimen/100323444), which Hackel et al. (2018) received as a silica specimen from the Missouri Botanical Garden DNA Bank. Because the previous study focused on a larger scale (i.e., grasses in Madagascar) and only several markers were used, posterior probabilities for most inner nodes of Hickeliinae were considerably low and prevent further discussion.

4.3. Paraphyly of the genus Nastus

The genus Nastus was originally published by Jussieu (1789) based on Nastus borbonicus as the type species. It is distributed in Madagascar with only the type species on Reunion Island. However, the result of plastid phylogenomic analysis resolved Nastus as polyphyletic and further confirmed the results of Zhou et al. (2017). The central point of incongruence in Nastus with Hackel et al. (2018) is in the placement of Nastus borbonicus: Hackel et al. (2018) analyzed ndhF and rps16 originally sequenced by Kelchner and Bamboo Phylogeny Group (2013), which is sister to three Malagasy Nastus but without statistical support. Our phylogeny rejects the current delimitation of Nastus and strongly suggests that it may now encompass two distinct genera. In addition to their allopatric nature, species currently treated in Nastus from Madagascar can be distinguished from Nastus borbonicus by a few morphological characteristics. All Nastus species from Madagascar, described by A. Camus (1925–1953), have determinate inflorescences with one-floret spikelets, which match the inflorescence structure of Nastus borbonicus from Reunion Island. The spikelet consists of five transitional glumes, one floret, and a rachilla extension usually with rudimentary floret. However, they differ from Nastus borbonicus in having slender culms that are erect with dropping tips (N. elongatus) or erect at lower parts with scrambling upper parts. Moreover, the species from Madagascar have a single branch bud at each node, which is borne below the supranodal ridge where the sheath scar curves downward, whereas Nastus borbonicus has multiple branch buds at each node which are borne above the sheath scar which is not curved. Malagasy Nastus species have a clumping habit with commonly short necks in the rhizome. However, the rhizomes have long necks in Nastus borbonicus, so that it does not form a clump. The fact that Jussieu based the genus on Nastus borbonicus, recovered here as its own lineage, suggests that other species of Nastus will need to be accommodated in a different, probably new genus. Further phylogenetic studies with broader sampling across its distribution range and evidence from nuclear genes are needed to clarify relationships between Malagasy species of Nastus and the type species, Nastus borbonicus.

5. Conclusion

This study shows that the plastome structure of Hickeliinae is largely conserved, with characteristics that are similar to those of other Bambusoideae species. Our plastid phylogenomic analysis provides a robust framework of Hickeliinae and confirms previous delimitation of genera based on morphological characters, although further phylogenetic analyses based on nuclear genes and morphological characters are still needed. Furthermore, our phylogeny suggests that the currently-defined genus Nastus is paraphyletic and might be divided into two different genera. However, given the reticulate evolutionary history of woody bamboos, this needs to be verified by nuclear data (Guo et al., 2019, 2021). We, therefore, recommend a taxonomic review of the genus Nastus on the basis of comprehensive phylogenomic study. Our work has demonstrated that comparative plastome analysis provides insight into the phylogeny of Hickeliinae and using complete plastomes can resolve the complex phylogenetic relationships. Our work also highlights the need for an evaluation of the conservation status of each species of the Malagasy Hickeliinae across all distributions and in various ecological niches, which is indispensable for protecting and sustainable utilizing Malagasy bamboos.

Author contributions

RAR conducted field survey and phylogenomic analysis, and drafted the manuscript; TH, MSV, HR and SD assisted in field sampling and herbarium work; MSV, TH and SD provided comments and revised the draft; MYZ and DZL conceived the study and wrote the paper. All authors contributed to the paper and gave final approval.

Declaration of competing interest

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Appendix A. Supplementary data

The following are the Supplementary data to this article:

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