A large-scale chloroplast phylogeny of the Lamiaceae sheds new light on its subfamilial classification


Lamiaceae, the sixth largest angiosperm family, contains more than 7000 species distributed all over the world. However, although considerable progress has been made in the last two decades, its phylogenetic backbone has never been well resolved. In the present study, a large-scale phylogenetic reconstruction of Lamiaceae using chloroplast sequences was carried out with the most comprehensive sampling of the family to date (288 species in 191 genera, representing approximately 78% of the genera of Lamiaceae). Twelve strongly supported primary clades were inferred, which form the phylogenetic backbone of Lamiaceae. Six of the primary clades correspond to the current recognized subfamilies Ajugoideae, Lamioideae, Nepetoideae, Prostantheroideae, Scutellarioideae, and Symphorematoideae, and one corresponds to a portion of Viticoideae. The other five clades comprise: 1) Acrymia and Cymaria; 2) Hymenopyramis, Petraeovitex, Peronema, and Garrettia; 3) Premna, Gmelina, and Cornutia; 4) Callicarpa; and 5) Tectona. Based on these results, three new subfamilies—Cymarioideae, Peronematoideae, and Premnoideae—are described, and the compositions of other subfamilies are updated based on new findings from the last decade. Furthermore, our analyses revealed five strongly supported, more inclusive clades that contain subfamilies, and we give them phylogenetically defined, unranked names: Cymalamiina, Scutelamiina, Perolamiina, Viticisymphorina, and Calliprostantherina.


The circumscriptions of Lamiaceae and Verbenaceae have changed dramatically in the past 25 years as a consequence of the discovery that both families were polyphyletic as traditionally circumscribed (e.g., by Bentham1 and Briquet2 for Lamiaceae and by Briquet3 for Verbenaceae; see Cantino4 for a summary of traditional classifications of Lamiaceae). The polyphyly of Lamiaceae was first proposed based on gynoecial morphology5, palynology6,7, and phylogenetic analyses of non-DNA data4,8 and subsequently corroborated by molecular research9,10. Based on these studies, the traditionally circumscribed family Verbenaceae was thought to be paraphyletic (as also implied earlier by Cronquist11 using different terms), but more recent molecular studies of Lamiales12,13,14,15 have shown that Verbenaceae as traditionally circumscribed were polyphyletic, with genera such as Vitex L., Clerodendrum L., and Callicarpa L. being more closely related to the traditional Lamiaceae than they are to Verbenaceae s. str. In an attempt to delimit monophyletic families, Cantino8 resurrected Junell’s5 proposed transfer of about 50 genera (in subfamilies Caryopteridoideae, Chloanthoideae, Viticoideae, and tribe Monochileae) of Verbenaceae to Lamiaceae, leaving only subfamily Verbenoideae in the reconstituted Verbenaceae. Wagstaff et al.10 additionally found that Congea Roxb., a representative of subfamily Symphorematoideae of Verbenaceae, which was not transferred to Lamiaceae by Cantino8, should be included in Lamiaceae. Harley et al.16 adopted the expansion of Lamiaceae and proposed a subfamilial classification of the family, which is the first global, genus-level treatment of the entire family in more than a century (since Briquet2).

As presently circumscribed16, Lamiaceae are the largest family-level clade within Lamiales17, an order comprising 26 families and over 20,000 species18. They are cosmopolitan in distribution and occur as herbs, shrubs, lianas, and trees. Economically important products include teak wood (Tectona), oil of peppermint (Mentha) and patchouli (Pogostemon), and various culinary herbs—e.g., rosemary (Rosmarinus), thyme (Thymus), basil (Ocimum), oregano (Origanum), sage (Salvia), and both spearmint and peppermint (Mentha). Recent phylogenetic studies of angiosperms19, and especially Lamiales13,15, place both Lamiaceae and Verbenaceae within a large clade called “core Lamiales”13, where Lamiaceae are sister to a well-supported clade comprising Orobanchaceae and several small families (Mazaceae, Paulowniaceae, Phrymaceae, Rehmanniaceae), and Verbenaceae are sister to the small African family Thomandersiaceae. The early misunderstanding of the proper division between Lamiaceae and Verbenaceae relied on macroscopic features of the ovary, such as the degree to which it is divided and the placement of the style. However, what Junell5 recognized and Cantino4 later brought to the attention of botanists, is the fundamental distinction between where the ovules attach to the ovary wall relative to the false septa that divide each carpel into two single-seeded chambers; ovules in Lamiaceae attach to the sides of an inrolled carpel wall, whereas ovules in Verbenaceae attach directly to the margins of the false carpel septa. In addition, the inflorescence is fundamentally cymose in Lamiaceae versus racemose in Verbenaceae, but this is not a consistent distinction because a recemoid inflorescence has independently evolved in several subgroups of Lamiaceae. In general, Lamiaceae can be recognized by a combination of traits, including opposite leaves, bilaterally symmetric flowers with four stamens, and ovaries consisting of two fused carpels, each divided into one-seeded chambers. However, most Verbenaceae also exhibit these traits, albeit with much less variation in floral form, hence the long-standing belief that the two families are each other’s closest relatives. Only the advent of molecular phylogenetic studies9,10,15 showed conclusively that this was not the case.

In Lamiaceae, Harley et al.16 recognized 236 genera (comprising more than 7000 species), 226 of which were assigned to seven subfamilies: Ajugoideae, Lamioideae, Nepetoideae, Prostantheroideae, Scutellarioideae, Symphorematoideae and Viticoideae. Ten genera that could not be placed in a subfamily were listed as incertae sedis: Acrymia Prain, Callicarpa, Cymaria Benth., Garrettia Fletch., Holocheila (Kudo) S. Chow, Hymenopyramis Wall. ex Griff., Ombrocharis Hand.-Mazz., Peronema Jack, Petraeovitex Oliv., and Tectona L. A decade later, Harley et al.’s16 classification has been widely adopted, and new evidence has incrementally improved the classification. The monophyly of five of the seven subfamilies (Ajugoideae, Lamioideae, Nepetoideae, Prostantheroideae, and Scutellarioideae) has been supported by molecular studies20,21,22,23,24,25,26. Within subfamilies, intergeneric relationships have been illuminated to varying degrees in Ajugoideae22,27, Lamioideae21,23,25,26,28,29,30,31,32,33, Nepetoideae34,35,36,37,38,39,40,41,42,43, Prostantheroideae44,45,46, and Scutellarioideae24, and tribal subdivisions in Lamioideae have been proposed and updated21,23,26. However, the monophyly of two subfamilies, Symphorematoideae and Viticoideae, still has not been satisfactorily examined. The former is well characterized by morphological characters (e.g., woody climbing stems, capitate inflorescences surrounded by an involucre of 3–6 bracteoles, polysymmetric flowers, and ovary with incomplete septum), some of which are probably synapomorphies, but its monophyly has not been tested with DNA data because no molecular study has included more than one representative9,10,21,23,24,25,47. In contrast, there is now strong evidence that subfamily Viticoideae, as circumscribed by Harley et al.16, is not monophyletic. Its members fall into two clades that are not sister groups10,23,24,25,43,47, with Vitex (grouped with Paravitex H. R. Fletcher, Petitia Jacq., Teijsmanniodendron Koord., Tsoongia Merr., and Viticipremna H. J. Lam) being the largest genus in one clade and Premna (grouped with Cornutia L. and Gmelina L.) in the other. Based on these results, Paravitex, Tsoongia, and Viticipremna were reduced to synonymy with Vitex47, and Cornutia, Gmelina, and Premna were assigned to a provisional subfamily, “Premnoideae”18,48.

Of the ten genera considered to be incertae sedis by Harley et al.16, Holocheila has since been shown to be a member of tribe Pogostemoneae in subfamily Lamioideae25, and Ombrocharis has been shown to be part of tribe Elsholtzieae in subfamily Nepetoideae43. The other eight genera have still not been placed in subfamilies, but several molecular studies have shed light on their relationships: Acrymia and Cymaria form a moderately supported clade23,25,26; Hymenopyramis, Peronema and Petraeovitex25,47 or Hymenopyramis, Petraeovitex and Garrettia25 group together; Callicarpa is sister to the rest of the family21,23 or groups with subfamily Prostantheroideae15; Tectona emerges in various positions21,23,47.

Although all ten genera incertae sedis and all seven subfamilies have been included in molecular studies cited above, no single study has included all of them, and the phylogenetic backbone of the family remains poorly resolved. The present study employs the most broadly comprehensive sampling of the family to date, including representatives of every subfamily and tribe, all ten of the genera incertae sedis of Harley et al.16, and a substantially larger sample of the mainly tropical and subtropical taxa Premna, Callicarpa, Gmelina, Tectona, and Symphorematoideae than in previous studies. We are using five plastid DNA regions to infer a large-scale phylogeny of the whole family with four objectives, to: (1) increase resolution of the phylogenetic backbone of Lamiaceae, (2) determine the phylogenetic positions of the genera incertae sedis, (3) assess relationships among subfamilies, and (4) test the monophyly of Symphorematoideae.


The number of sequences, new sequences generated in this study, aligned length of sequences, proportion of missing data, parsimony informative characters and indels, tree length, consistency index (CI), retention index (RI), and evolutionary model, for separate and combined data sets are summarized in Table 1.

Table 1 Properties of data partitions used in this study and tree statistics.

MP and ML analyses of separate data sets (matK, ndhF, rbcL, rps16, and trnL-F) did not yield fully resolved gene trees for the whole family. Generally, MP and ML analyses of the same data set yielded similar supported clades (Supplementary Figs S1–S5). Trees generated from different data sets had variable topological structure, but there were several comparable clades among these different trees (Table 2).

Table 2 Comparison of support values for subfamilial or above nodes in the different analyses.

Based on the combined data sets D270 and D155, all MP, ML and BI analyses yielded very similar topologies, and this was true regardless of whether gaps were treated as simple indels or as missing data. Twelve well-supported primary clades were obtained in all analyses (Figs 1, 2, 3, 4; Supplementary Figs S6–S12). A simplified phylogenetic tree shows the phylogenetic backbone of Lamiaceae (Fig. 1), and the 50% majority-rule consensus tree from the BI analysis of the combined D270 data set with simple gap coding shows detailed relationships (Figs 2 and 3). Six of the 12 primary clades in Fig. 1 correspond to subfamilies Ajugoideae, Lamioideae, Nepetoideae, Prostantheroideae, Scutellarioideae, and Symphorematoideae, as recognized by Harley et al.16 and Olmstead18, and one corresponds to subfamily Viticoideae s. str. as recognized by Bramley et al.47. The monophyly of Symphorematoideae was confirmed for the first time, with all three genera sampled in one study (Fig. 2 and 3). Besides these subfamilial clades, the other five primary clades comprise: 1) Acrymia and Cymaria; 2) Hymenopyramis, Petraeovitex, Garrettia, and Peronema; 3) Premna, Gmelina, and Cornutia; 4) Callicarpa; and 5) Tectona. The relationships among these 12 clades were inferred with varying degrees of support. Callicarpa and Prostantheroideae group together in all of the combined-data analyses, with support ranging from low to high, and the Callicarpa-Prostantheroideae clade usually emerges as sister to the remaining Lamiaceae. Symphorematoideae and Viticoideae s. str. are sister groups in all combined-data analyses with high support. Acrymia-Cymaria, Scutellarioideae, and Hymenopyramis-Petraeovitex-Garrettia-Peronema are successive sister groups to Lamioideae (Fig. 2), with each node highly supported in all combined-data analyses (Fig. 1). Overall, the 12 primary clades cluster into four larger clades. Relationships among the four larger clades are poorly resolved, but each usually received moderate to high support in our analyses (Fig. 1: clade I–IV). Support values for the above-mentioned clades are summarized in Table 2. Phylogenetically defined names (names ending in –ina in Fig. 1) are hereby proposed for five clades that are moderately to strongly supported in our analyses and do not already have genus or subfamily names.

Figure 1: Phylogenetic backbone of Lamiaceae based on simplification of trees generated from the analyses of the combined cpDNA (matK + ndhF + rbcL + rps16 + trnL-F) dataset D270.

Color-coded circles above branches indicate support values from BI, ML and MP analyses of the combined dataset D270, with or without gaps coded respectively, while those below branches indicate support values from BI, ML and MP analyses of the combined dataset D155, with or without gaps coded respectively. Subfamilies recognized by Olmstead46 (Ajugoideae, Lamioideae, Nepetoideae, Prostantheroideae, Scutellarioideae, Symphorematoideae, and Viticoideae s. str.) are shown in black bold font, while new subfamilies (Cymarioideae, Peronematoideae and Premnoideae) and two genera (Callicarpa and Tectona) that we do not assign to a subfamily are in red bold font. The arrows show the clade node of Lamiaceae and the nodes of five new clades (Cymalamiina, Scutelamiina, Perolamiina, Viticisymphorina, and Calliprostantherina).

Figure 2

Bayesian 50% majority-rule consensus tree (box on the top left corner shows the topology) based on the combined cpDNA (matK + ndhF + rbcL + rps16 + trnL-F) dataset D270, with gaps treated as simple indels, showing the taxa from Lamioideae, Cymarioideae, Scutellarioideae, Peronematoideae, Premnoideae, Ajugoideae, and Tectona. The topologies of the ML and MP trees are congruent with the BI tree. Bayesian posterior probability values ≥ 0.90 are marked with bold lines. Bootstrap values ≥ 50% in ML and MP analyses are plotted above the branches, successively, while “-” indicates support values of less than 50%. Multiple accessions of the same species are numbered according to Supplementary Table S1. A single generic name indicates that the combined sequences pooled from different species of the genus. Subfamilies and tribes recognized by Olmstead18 were covered by gray boxes with different grey level, while new subfamilies and clades proposed in this study were covered by pink boxes and marked in red bold font.

Figure 3

Bayesian 50% majority-rule consensus tree (box on the top left corner shows the topology) based on the combined cpDNA (matK + ndhF + rbcL + rps16 + trnL-F) dataset D270, with gaps treated as simple indels, showing the taxa from Nepetoideae, Viticoideae s. str., Symphoremoideae, Callicarpa, and Prostantheroideae. The topologies of the ML and MP trees are congruent with the BI tree. Bayesian posterior probability values ≥ 0.90 are marked with bold lines. Bootstrap values ≥ 50% in ML and MP analyses are plotted above the branches, successively, while “-” indicates support values of less than 50%. Multiple accessions of the same species are numbered according to Supplementary Table S1. A single generic name indicates that the combined sequences pooled from different species of the genus. Subfamilies and tribes recognized by Olmstead18 were covered by gray boxes with different grey level, while new subfamilies and clades proposed in this study were covered by pink boxes and marked in red bold font.

Figure 4: The Bayesian 50% majority-rule consensus phylogram based on combined cpDNA (matK + ndhF + rbcL + rps16 + trnL-F) dataset D155, with gaps treated as simple indels.

The topologies of the ML and MP trees are congruent with the BI tree. Support values displayed on the branches follow the order BI-PP/ML-BS/MP-BS (“−” Indicates support values of less than 0.90 in BI or 50% in ML and MP analyses, respectively). The bold lines indicate that the three support values get full scores simultaneously. Multiple accessions of the same species are numbered according to Supplementary Table S1. A single generic name represented that the combined sequences pooled from different species of the genus. Subfamilies recognized by Olmstead45 were covered by gray boxes with different grey level, while new subfamilies (Cymarioideae, Peronematoideae, and Premnoideae) and clades (Callicarpa and Tectona) proposed in this study were covered by pink boxes and marked in red bold font.


Our phylogenetic reconstruction of Lamiaceae, on the basis of the most comprehensive sampling of Lamiaceae to date, builds on prior studies using chloroplast DNA markers9,10,21,22,23,24,25,27,28,31,32,33,34,35,36,37,38,39,40,41,43,45,46,47,49,50,51,52,53. All of our analyses of the concatenated datasets revealed 12 highly supported primary clades (Figs 1, 2, 3, 4), which are grouped into four moderately to highly supported larger clades (Fig. 1: clade I–IV). This set of four clades has not been identified in any previous published analysis but is consistent with the unpublished results of another combined analysis of three cpDNA regions (ycf1 + ycf1–rps15 + trnL-F; B. Drew, pers. comm.). Of the 12 primary clades, five correspond to subfamilies Ajugoideae, Lamioideae, Nepetoideae, Prostantheroideae, and Scutellarioideae as recognized both by Harley et al.16 and Olmstead18. We have no additional findings on these subfamilies relative to previous molecular studies21,22,23,24,25,26,43,46, so we will focus our discussion on the other seven primary clades. One of these clades corresponds to Symphorematoideae recognized by Harley et al.16 and Olmstead18, and another corresponds to Viticoideae s. str. recognized by Bramley et al.47. These two clades are sister groups in all our combined-data analyses. The other five primary clades comprise Acrymia-Cymaria, Hymenopyramis-Petraeovitex-Peronema-Garrettia, Premna-Gmelina-Cornutia, Callicarpa, and Tectona. Eight genera listed as incertae sedis in Harley et al.16 are included in these five clades. Resolution of their phylogenetic placements makes it possible to improve the subfamilial classification of the Lamiaceae.


The clade comprising Callicarpa and Prostantheroideae, which we are naming Calliprostantherina (see Phylogenetic Nomenclature, below), emerged as sister to the remaining Lamiaceae in our phylogeny. This finding agrees with the large-scale phylogenetic analysis of Lamiidae15, while in other analyses, Callicarpa9,21,23 or Symphorematoideae (represented by Congea)10,24,25 was inferred to be sister to the rest of Lamiaceae. Inconsistency among published trees probably reflects taxon sampling or insufficient data, since these conditions could impact the accuracy of phylogenetic analyses54,55. Outgroups used by Scheen et al.21, Bendiksby et al.23, Li et al.24, and Chen et al.25 are distantly related to the Lamiaceae, and Prostantheroideae were not sampled by Schäferhoff et al.13. In the present study, outgroups were selected from Mazaceae, Orobanchaceae, Paulowniaceae, and Phrymaceae, which together form the sister group to Lamiaceae in recent studies of Lamiales12,13,14,15, and the ingroup was more comprehensively and densely sampled than in previous studies. Thus, there is reason to have greater confidence in our inference of a Callicarpa-Prostantheroideae clade that is sister to the remaining Lamiaceae than the different inferred positions of these taxa in some previous studies.


The clade comprising the subfamilies Symphorematoideae and Viticoideae s. str., which we are naming Viticisymphorina (see Phylogenetic Nomenclature, below), was strongly supported in all our analyses, consistent with some previous studies23,47. Each subfamily in this clade was confirmed to be monophyletic for the first time (Figs 1, 2, 3, 4, Table 2). Though Symphorematoideae is well characterized by many morphological characters, its monophyly had never been tested in previous molecular studies because only one representative had been included9,10,21,23,24,25,47. With all three genera included in the present study, Symphorematoideae was confirmed to be monophyletic (Figs 1, 2, 3, 4, Table 2). Viticoideae as circumscribed by Harley et al.16 have been shown to form two clades that are not sister groups10,23,25,43,47, with Vitex (grouped with Paravitex, Petitia, Teijsmanniodendron, Tsoongia, and Viticipremna) being the largest genus in one clade and Premna (grouped with Cornutia and Gmelina) the largest genus in the other. After Premna, Cornutia, and Gmelina were removed from Viticoideae18 and Paravitex, Tsoongia, and Viticipremna were reduced to synonymy with Vitex47, the remaining Viticoideae consist of only four genera: Petitia, Pseudocarpidium Millsp., Teijsmanniodendron, and Vitex. We included representatives of all four of these genera in a single analysis for the first time here and the monophyly of Viticoideae s. str. was strongly supported (Figs 1, 2, 3, 4, Table 2).

Symphorematoideae and Viticoideae s. str. are morphologically distinct from each other. Symphorematoideae are woody climbers with simple leaves, 3–7-flowered capitate inflorescences with accrescent bracteoles, whereas Viticoideae s. str. are generally shrubs or trees that have simple or palmately compound leaves and lack the distinctive inflorescence structure of Symphorematoideae. However, the two subfamilies are putatively connected by several anatomical structures: 1) Ovaries without a false septum are rare in other Lamiaceae, but can be found both in Symphorematoideae and Viticoideae s. str. 2) In Symphorematoideae, orthotropous and pendulous ovules are borne in the free apex of the locules16. Ovules in most Lamiaceae are anatropous or hemianatropous. Junell5 noted that the distinctive placentation in Symphorematoideae could easily be derived from the type of placentation found in many Viticoideae.


This clade, comprising Premna, Gmelina and Cornutia, has been partially recovered in previous molecular phylogenetic analyses10,24,25,43, in which Premna and Gmelina always grouped together. Cornutia was first included by Bendiksby et al.23 and revealed to be sister to a clade containing Premna, Gmelina, and Tectona (though the inclusion of Tectona in that clade conflicts with all other studies). In all of our combined analyses, the Premna-Gmelina-Cornutia clade was strongly supported (Table 2). This clade is part of a larger clade that also includes Ajugoideae, Hymenopyramis-Petraeovitex-Garrettia-Peronema, Scutellarioideae, Acrymia-Cymaria and Lamioideae, consistent with the findings in Chen et al.25. Though traditionally placed in Viticoideae3,16, previous studies10,23,24,25,43,47 as well as the present one have shown that the Premna-Gmelina-Cornutia clade is not sister to the rest of Viticoideae sensu Harley et al.16. Furthermore, these three genera cannot be included in any other established subfamily based on our results. In a paper intended to contrast conventional and phylogenetic nomenclature, Cantino et al.56 informally referred to the Premna-Gmelina clade (the position of Cornutia being unknown at that time) as Premnoideae under rank-based nomenclature and Premnina under phylogenetic nomenclature, and the former name was provisionally adopted by Olmstead18,48. Below we formally describe the new subfamily Premnoideae B. Li, R. G. Olmstead & P. D. Cantino.


This clade comprises Petraeovitex, Peronema, Hymenopyramis and Garrettia. The first three of these were inferred to form a well-supported clade25,47 that is sister to the Scutellarioideae-Acrymia-Cymaria-Lamioideae clade25. The same sister position to Scutellarioideae-Acrymia-Cymaria-Lamioideae was found for Garrettia, which was first included by Bendiksby et al.23. When Garrettia, Hymenopyramis, and Petraeovitex were included in the same analysis, they formed a moderately supported clade25. In our combined analyses, the four genera form a highly supported clade that is sister to a larger clade comprising of Scutellarioideae, Acrymia-Cymaria and Lamioideae (Figs 1, 2, 3, 4, Table 2). Olmstead18 suggested that a new name should be provided to accommodate the Hymenopyramis-Petraeovitex-Peronema clade, while Garrettia was still listed as having uncertain subfamilial placement in his A Synoptical Classification of the Lamiales (Version 2.4). Based on the present phylogeny, the clade comprising Hymenopyramis, Petraeovitex, Garrettia, and Peronema cannot be assigned to any established subfamily, thus we here propose a new subfamilial name: Peronematoideae B. Li, R. G. Olmstead & P. D. Cantino. Formal description of the new subfamily is provided below.


This small clade comprising Acrymia and Cymaria received high support in all our analyses of combined dataset D270, as well as in BI, ML, and MP analyses of D155 with gaps coded. It was inferred to be sister to subfamily Lamioideae with strong support in all analyses (Figs 1, 2, 3, 4, Table 2). Our findings corroborate previous molecular phylogenetic analyses, where Cymaria21 or Acrymia-Cymaria23,25 was revealed to be closely related to Lamioideae. Now that the phylogenetic relationships seem to be well established, a taxonomic decision is needed whether to expand Lamioideae to include these two genera or name a new subfamily to accommodate them. The two approaches are equally consistent with the molecular phylogenetic results; i.e., both Lamioideae s. str. and a broader Lamioideae, expanded to include Acrymia and Cymaria, are well supported in our analyses and previous studies23,25. Bendiksby et al.23 and Chen et al.25 have argued that an expanded Lamioideae would be more morphologically heterogeneous and difficult to diagnose, and they therefore recommended excluding Acrymia and Cymaria from Lamioideae. Because the Acrymia-Cymaria clade was only moderately supported in their analyses, Chen et al.25 noted that if future evidence were to strongly corroborate the existence of this clade, a new subfamily could be named to accommodate them. This hypothesis is confirmed with strong confidence in our analyses (Figs 1, 2, 3, 4, Table 2); therefore, we hereby erect the new subfamily Cymarioideae B. Li, R. G. Olmstead & P. D. Cantino and formally describe it below.

Taxonomy and Nomenclature

An Updated Subfamilial Classification of Lamiaceae

The most recent and widely adopted classification of Lamiaceae was proposed by Harley et al.16 in the first global, genus-level treatment of the entire family in more than a century since Briquet2. Harley et al.’s landmark work includes 226 genera assigned to seven subfamilies (Ajugoideae, Lamioideae, Nepetoideae, Prostantheroideae, Scutellarioideae, Symphorematoideae, and Viticoideae), and ten genera listed as incertae sedis (Acrymia, Callicarpa, Cymaria, Garrettia, Holocheila, Hymenopyramis, Ombrocharis, Peronema, Petraeovitex, and Tectona). A decade later, numerous new findings have improved the classification incrementally. The results reported here provide the basis for a revised subfamilial classification. We take this opportunity to describe three new subfamilies and to update the subfamilial classification of the family incorporating new findings since Harley et al.16. For each subfamily, we provide a brief summary of its historical classification and presently understood phylogenetic position, generic and species diversity, morphology, synapomorphies, and distribution. Of the ten genera treated as incertae sedis by Harley et al.16, there are only two that we do not assign to a subfamily—Callicarpa and Tectona; these genera are inserted among the subfamilies in positions consistent with the phylogeny in Fig. 1.

Prostantheroideae Luerssen

This endemic Australian subfamily includes 17 genera and ca. 300 species belonging to two major clades, Chloantheae (12 genera) and Westringieae (5 genera). Prior to the cladistic study of Cantino4, these tribes were usually placed in Verbenaceae (or Chloanthaceae57,58) and Lamiaceae, respectively (e.g., Briquet2,3). However, based on gynoecial anatomy, Junell5 transferred “Chloanthoideae” (i.e., Chloantheae) to Lamiaceae and suggested that it shares a common origin with “Prostantheroideae” (i.e., Westringieae). Cantino et al.59 first placed the two groups together in a subfamily (“Chloanthoideae”). Monophyly of each tribe (excluding Spartothamnella Briq. and Tectona from Chloantheae, contrary to Munir60 and Cantino et al.59, respectively) and of the combined Prostantheroideae was confirmed by molecular phylogenetic analysis20, which also produced the first evidence that Callicarpa is sister to Prostantheroideae. Phylogenetic studies of Prostantheroideae20,44,45,46 (as well as from T. Wilson and B. Conn, pers. comm.) have revealed that several genera are not monophyletic as currently circumscribed. Recent and ongoing studies have led to abandonment of the genera Wrixonia F. Muell. (included in Prostanthera Labill.)61 and Mallophora Endl. (included in Dicrastylis J. Drumm. ex W. H. Harvey)62, the reinstatement of Dasymalla Endl. and Quoya Gaudich. and addition of Muniria N. Streiber & B. J. Conn comprising species previously assigned to Pityrodia R. Br.63, and indications that additional realignments to several genera will be forthcoming44,64 (also T. Wilson, pers. comm.). A probable synapomorphy is a dry schizocarp that splits into four one-seeded mericarps. This feature also characterizes several other clades within Lamiaceae, but our results indicate that it evolved independently in each. Because this fruit type is found in all members of Westringieae and in Brachysola Rye, which is sister to the rest of Chloantheae4,20,45, it is the most parsimonious assignment to the most recent common ancestor of Prostantheroideae.

Callicarpa Linnaeus

Callicarpa contains about 140 species occurring in both temperate and tropical regions16. The plants are small trees or shrubs with actinomorphic, 4–5 (−7)-parted flowers and drupaceous fruits. Despite being one of the largest genera in Lamiaceae, its phylogenetic position had not previously been confirmed. In previous molecular studies, Callicarpa was included with only one or few representatives, and has been inferred to be sister to the rest of the family9,21,23, to group with subfamily Prostantheroideae15,20,43, or to be variably isolated in different positions10. Bramley49 sampled more representatives and indicated that Callicarpa is monophyletic, but she could not infer its phylogenetic position because of poor sampling from the whole family. In the present study, Callicarpa was sampled much more extensively (18 spp.), taking into consideration its morphological and geographic breadth and its infrageneric classification. In all our analyses, the monophyly of Callicarpa was well supported (Figs 1, 2, 3, 4; Table 2). A sister relationship between Callicarpa and subfamily Prostantheroideae was moderately to highly supported in analyses of the combined dataset D270 (Figs 1, 2, 3, Table 2), as well as in BI and ML analyses of the combined dataset D155 (Fig. 4).

Symphorematoideae Briquet

The subfamily has three genera: Congea (ca. 7 species), Sphenodesme Jack (ca. 14 species) and Symphorema Roxb. (3 species). All genera are endemic to continental Asia (India to Indochina and southern and eastern China) and parts of Malesia (Peninsular Malaysia, Sumatra, Borneo, Java, Tanimbar Islands, and the Philippines). Congea tomentosa Roxb. and to a lesser extent C. griffithiana Munir are cultivated as ornamental climbers. There are several morphological traits that unite the three genera. All are climbers with inflorescences of 3–7-flowered capitate cymes. These are usually surrounded by conspicuous bracteoles, often coloured and accrescent. Flowers of Sphenodesme are 5 or 6-merous; the flowers of Symphorema are 6 to 16 (–18)-merous. The corolla of Congea is 2-lipped, but the corollas of Sphenodesme and Symphorema are actinomorphic. The ovaries are incompletely 2-locular, and the ovules are orthotropous and pendulous. Although unique to this subfamily, the ovary type was interpreted by Junell5 as being derived from that found in genera of “Viticoideae” (in which Junell included not only Viticoideae s. str. but also Callicarpa, Tectona, Premnoideae, Peronematoideae, Cymarioideae, and Ajugoideae in our classification). The fruit in all three genera is indehiscent, weakly drupaceous or dry, and is 1 (−2) -seeded by abortion.

Viticoideae Briquet

Viticoideae, as circumscribed here, includes only three genera: Vitex (ca. 250 spp.), Teijsmanniodendron (23 spp.), and Pseudocarpidium (9 spp.). In contrast, Viticoideae sensu Harley et al.16 included ten genera (viz., Petitia, Cornutia, Premna, Viticipremna, Tsoongia, Paravitex, Vitex, Teijsmanniodendron, Gmelina, and Pseudocarpidium). Molecular studies, initially by Wagstaff and Olmstead10, had identified two distinct clades, one centered on Vitex and another including Gmelina, Cornutia, and Premna. Phytochemical studies65 hinted at the same relationships, finding that phenolic compounds present in Premna or Gmelina were absent in Vitex, Petitia, and Teijsmanniodendron. Because several smaller viticoid genera were not included in these early analyses, the circumscription of the subfamily was not altered by Harley et al.16. Bramley et al.47 further elucidated the relationships among the viticoid genera, focusing particularly on Southeast Asian taxa traditionally allied to Vitex. Based on their results, Viticipremna, Tsoongia, and Paravitex were included in Vitex, reducing the number of viticoid genera to seven. The generic status of Petitia and Pseudocarpidium was unchanged, because of poor support for the position of the former, lack of any data for the latter, and poor sampling among Neotropical taxa. In the present study, we find sufficient evidence to include Petitia, but not Pseudocarpidium, in Vitex. Similarly, the generic status of Teijsmanniodendron remains problematic. Neither the analyses of Bramley et al.47 nor our analyses provide convincing support to include Teijsmanniodendron in Vitex. Identification of species in these two genera is often confused; the sole morphological character that can be used to delimit them in most cases is a swelling present at the base and apex of the petiole in Teijsmanniodendron. Traditionally, Teijsmanniodendron species were also recognised by their capsule-like rather than drupaceous fruit that is 1-seeded (by abortion)66, but a reduction in the number of mature seeds can also occur in Vitex species.

Viticoideae are distributed predominantly in the Tropics (Vitex throughout; Teijsmanniodendron in Malesia; Pseudocarpidium in the Caribbean), although there are a few temperate species of Vitex. Madagascar may be home to a number of currently unrecognized species of Vitex67. Analysis of a greater number of viticoid taxa could result in further changes to generic boundaries in this subfamily. Possible synapomorphies for the subfamily are phytochemical (see Pedersen65). There has been no comparative study of morphological or anatomical characters including all of the viticoid genera aside from Junell’s5 work on gynoecial structure. Although Junell noted that Vitex, Petitia, Pseudocarpidium, and the other genera now recognized as Vitex have a very similar ovary structure, he found some differences in Teijsmanniodendron. Further comparative studies including subfamily Viticoideae, particularly focusing on gynoecial structure, may elucidate unifying characters.

Nepetoideae (Dumortier) Luerssen

Nepetoideae is the largest subfamily of Lamiaceae, containing almost half of the genera and species. It now contains 118 genera (compared to 105 recognized by Harley et al.16) and ca. 3400 species, which are widely distributed across tropical and temperate regions of the northern and southern hemispheres but with few native species in Australia and New Zealand. Probable synapomorphies for Nepetoideae include hexacolpate and three-celled pollen, investing embryos, myxocarpy, gynobasic style, and the presence of rosmarinic acid4,16,68,69,70,71. Three tribes are now recognized within Nepetoideae16: Elsholtzieae, Mentheae, and Ocimeae. The monophyly of each of these tribes is well supported by molecular phylogenetic studies34,37,40,43,72, but there are conflicting findings about relationships among the three tribes.

There have been several genus-level changes since the treatment of the subfamily by Harley et al.16. Bräuchler et al.72 described a new genus Killickia Bräuchler, Heubl & Doroszenko from South Africa. Harley and Pastore73 did a major genus-level revision of Hyptidinae, recognizing 12 genera that were not recognized by Harley et al.16. Nine of them were new (Cantinoa Harley & J. F. B. Pastore, Cyanocephalus (Pohl ex Benth.) Harley & J. F. B. Pastore, Eplingiella Harley & J. F. B. Pastore, Gymneia (Benth.) Harley & J. F. B. Pastore, Leptohyptis Harley & J. F. B. Pastore, Martianthus Harley & J. F. B. Pastore, Medusantha Harley & J. F. B. Pastore, Oocephalus (Benth.) Harley & J. F. B. Pastore, and Physominthe Harley & J. F. B. Pastore), and the other three were resurrected (Condea Adans., Eriopidion Harley, and Mesosphaerum P. Browne). Drew et al.42 synonymized Chaunostoma Donn. Sm. and Neoeplingia Ramam., Hiriart & Medrano with Lepechinia Willd. Chen et al.43 resurrected Keiskea Miq. (included in Collinsonia L. by Harley et al.16) and showed that Ombrocharis (unassigned to subfamily by Harley et al.16) is sister to Perillula Maxim. within tribe Elsholtzieae. Drew and Sytsma37 found Heterolamium C. Y. Wu to be nested within Meehania Britton, but Deng et al.74 found that the specimen of Heterolamium studied by Drew and Sytsma41 was misidentified and was in fact a member of Meehania. Thus, the systematic position of Heterolamium within Nepetoideae is still uncertain.

Tectona Linnaeus f

Tectona is a genus of large trees comprising three species distributed from India to southeast Asia. The large drupaceous fruits contain a hard four-celled endocarp and are enclosed in an enlarged persistent calyx. Tectona has been included in several molecular studies9,10,21,23,47, but its phylogenetic position has never been determined definitively. It has been inferred to be sister to a clade comprising Hymenopyramis-Petraeovitex-Peronema and Premna-Gmelina47, to a large clade containing Ajugoideae, Lamioideae, Scutellarioideae, Peronema-Petraeovitex, and Premna-Gmelina-Cornutia (B. Drew, pers. comm.), to another larger clade comprising Ajugoideae, Lamioideae, Premna-Gmelina, Prostantheroideae, Scutellarioideae, and Vitex-Petitia10, or to group with Gmelina21,23. In our more comprehensive analyses, Tectona is inferred to be sister to a large clade comprised of Lamioideae, Acrymia-Cymaria, Scutellarioideae, Hymenopyramis-Petraeovitex-Garrettia-Peronema, Ajugoideae, and Premna-Gmelina-Cornutia, with moderate to strong support in BI and ML analyses of both datasets D270 and D155, with or without gaps coded (Figs 1, 2, 3, 4). The distinct morphology of Tectona including an actinomorphic 5–7-lobed calyx and corolla, greatly enlarged and inflated persistent calyx, and 4-celled endocarp with small central cavity between the cells16, contributed to the difficulty of placing it in previous classifications. Our results suggest that Tectona is an early diverging lineage from the major clade IV (Figs 1, 2, 3, 4).

Premnoideae B. Li, R. G. Olmstead & P. D. Cantino, subfam. nov

Type: Premna L. in Mant. ii, 154. 1771.

Trees, shrubs, lianas, or rarely small herbs. Leaves simple, opposite, usually aromatic. Inflorescence cymose, usually terminal, variable in form. Calyx tubular or campanulate, truncate or 4–5-toothed, often obscurely 2-lipped. Corolla blue, purple-violet, mauve, yellow, brownish or white, infundibular or hypocrateriform, 4–5-lobed, ±2-lipped or occasionally actinomorphic. Stamens 4 or posterior pair reduced to staminodes, didynamous or equal, included or slightly exserted, thecae separate, parallel to widely divergent; pollen usually tricolpate (4–5-colpate in Cornutia), tectate-perforate, psilate or suprareticulate. Ovary unlobed, stigma 2-lobed, equal or unequal; disc well developed (Cornutia) or absent (Premna, Gmelina). Fruit drupaceous, exocarp fleshy, pyrene hard, 4-seeded (sometimes3–1-seeded by abortion).

This new subfamily contains three genera: Premna (50–200 spp. in tropical to subtropical Asia, Africa, Australia, and the Pacific Islands), Gmelina (31 spp. in tropical and subtropical Asia to Australia and western Pacific Islands), and Cornutia (12 spp. in tropical America). The three genera were traditionally placed in subfamily Viticoideae of Verbenaceae3, and transferred to Lamiaceae together with the subfamily5,16,59, and then excluded from Viticoideae by Olmstead18 based on molecular evidence that Viticoideae is non-monophyletic if they are included23,47. A possible synapomorphy for Premnoideae is a drupaceous fruit with one four-seeded pyrene. However since a similar fruit structure is also found in Tectona and some species of Vitex, it may instead be a synapomorphy at a deeper level in the phylogeny with subsequent reversals. With the number of species estimated from 5075 to 20076, Premna now ranks among the most taxonomically difficult and complicated genera of Lamiaceae. Though some regional revisions of the genus have been done in recent decades77,78,79,80,81,82, there is no treatment of the genus throughout its range. A global taxonomic revision of Gmelina was published by de Kok83.

Ajugoideae Kosteletzky

Ajugoideae contains 26 genera and ca. 760 species and is cosmopolitan in distribution. A series of phylogenetic studies, which collectively included every genus except Monochilus Fisch. & C. A. Mey., have resolved most of the generic boundaries and relationships22,27,84,85,86,87,88. Our results find a small clade comprising Karomia Dop and Rotheca Raf. to be sister to the rest of the subfamily. Unpublished results by one of us (C. L. Xiang) indicate that Discretitheca P. D. Cantino and Glossocarya Wall. ex Griff. are close relatives of Rotheca. This clade of four genera is distributed from Africa to the Indian subcontinent, Southeast Asia, and Queensland. The rest of Ajugoideae comprises two large clades. One, with ca. 260 species, is primarily temperate and centered on Teucrium L. (this clade remains poorly studied). The other large clade, with ca. 425 species, is centered on Clerodendrum19,24,51,87. The latter clade comprises a primarily tropical clade, which includes Clerodendrum and related genera, and a primarily temperate clade, which includes Ajuga L., Trichostema L., Caryopteris Bunge, and related genera. Molecular analyses22,27,89 have also increased the number of genera accepted from 2416 to 26, with Huxleya Ewart now included in Clerodendrum, Faradaya F. Muell. included in Oxera Labill., and four genera (Kalaharia Baill., Ovieda L., Tetraclea A. Gray, and Volkameria L.) segregated from Clerodendrum. Probable synapomorphies of Ajugoideae include pollen exine with supratectal spines, spinules or verrucae, and exine with branched to granular columellae. These character states are widespread in Ajugoideae16,90,91 and rare (branched columellae) or absent (spinules and verrucae) elsewhere in the Lamiaceae.

Peronematoideae B. Li, R. G. Olmstead & P. D. Cantino, subfam. nov

Type: Peronema Jack in Malayan Misc. 2 (7): 18. 1822.

Shrubs, trees, and lianas. Leaves opposite, petiolate, simple or ternately, biternately, or pinnately compound. Inflorescence cymose, axillary, and/or terminal, highly variable in form. Calyx actinomorphic, 4–5-lobed, and usually accrescent (not accrescent in Peronema) in fruit. Corolla white to yellow, 4–5-lobed, and nearly actinomorphic to zygomorphic. Stamens 4 or posterior pair reduced to staminodes (Peronema), equal or didynamous, included or exserted, thecae parallel to divaricate, usually separate (confluent in Garrettia) at dehiscence; pollen tricolpate, tectate-perforate. Ovary unlobed, stigma 2-lobed, equal or unequal; disc absent or poorly developed. Fruit dry, globose or turbinate, glabrous or pubescent to villous, indehiscent or breaking into two or four mericarps, abscission-scar as long as the mericarp.

This new subfamily comprises four small, mostly tropical Asian genera that were treated as incertae sedis by Harley et al.16: Garrettia (1 sp., southwest China, Thailand, and Indonesia), Hymenopyramis (7 spp., India, China, and Indo-China), Peronema (1 sp., Thailand to Malaysia and western Indonesia), and Petraeovitex (8 spp., Burma, Thailand, Malaysia, Indonesia, Philippines, New Guinea, and Melanesia). Previously, Hymenopyramis, Peronema, and Petraeovitex have been placed in Caryopteridoideae3 or transferred to Viticoideae5, or Hymenopyramis was retained in Viticoideae but Peronema and Petraeovitex were transferred to Teucrioideae59. Garrettia was always placed in Caryopteridoideae92,93 before being transferred to Ajugoideae59. The four genera of Peronematoideae differ greatly in morphology and have never been linked in any previous classification, but Chen et al.25 has found some traits in common, including woody stems (small or climbing shrubs, lianas or large trees), white to yellowish corolla, unlobed ovary, nectar disc poorly developed or absent, and dry fruit. Each of these traits is probably either synapomorphic at a more inclusive level within Lamiaceae or plesiomorphic in the family as a whole25.

Scutellarioideae (Dumortier) Caruel

A taxon centered on Scutellaria was recognized as a distinct element within Lamiaceae in early classifications (e.g., Bentham1; Briquet2), often comprising only Scutellaria and the segregate genera, Perilomia Kunth and Salazaria Torr., now included within Scutellaria16,94. Early phylogenetic studies based on morphology4,8 and DNA sequences10 expanded this clade to include Renschia Vatke, Tinnea Kotschy ex Hook. f., and Holmskioldia Retz., the latter formerly assigned to Verbenaceae. The rediscovery of the extremely rare Wenchengia C. Y. Wu & S. Chow permitted Li et al.24 to confirm its placement in Scutellarioideae by Harley et al.16. A characteristic two lobed, untoothed calyx is shared by a clade of Scutellaria, Renschia, and Tinnea. Holmskioldia is sister to this clade and has an expanded saucer-shaped calyx with five, often indistinct, lobes, which form the dominant part of the floral display, unlike the other genera. Wenchengia is sister to the rest of the clade and has a two-lobed, but five-toothed calyx. Probable synapomorphies for Scutellarioideae include pericarps with tuberculate or elongate processes24, high densities of xylem fibers in the calyces95, and possibly racemose inflorescences (but they are cymose in Holmskioldia and most species of Tinnea, suggesting that independent origin of racemes within Scutellarioideae may be equally parsimonious). Scutellaria includes approximately 360 species, is cosmopolitan in distribution, occurs in a wide range of habitats, and includes annual and perennial herbs and shrubs. A global taxonomic revision of Scutellaria established infrageneric classification and reduced Harlanlewisia, Perilomia, and Salazaria to synonymy94. Tinnea includes 19 species, all endemic to Africa. The rest of the clade consists of small, narrowly endemic genera: Renschia (1–2 spp., Somalia), Holmskioldia (1 sp., southern Himalayas), and Wenchengia (1 sp., Hainan island, China).

Cymarioideae B. Li, R. G. Olmstead & P. D. Cantino, subfam. nov

Type: Cymaria Bentham in Edwards’ Bot. Reg. 15: t. 1292. 1830.

Shrubs and subshrubs. Leaves simple, opposite, petiolate, elliptic or ovate to rhombic, crenate to crenulate or repand. Cymes axillary, lax, long-pedunculate, with secund, monochasial branches, sometimes grading into a terminal paniculiform thyrse. Calyx campanulate, accrescent, broadly campanulate to urceolate or subglobose in fruit, 5-lobed, lobes equal to subequal, triangular. Corolla white to yellowish, 2-lipped, posterior lip entire to deeply 2-lobed, anterior lip with median lobe largest. Stamens 4, didynamous (anterior pair longer), included or exserted, thecae divaricate, confluent at dehiscence; pollen tricolpate, tectate-perforate, suprareticulate, columellae simple to sparsely branched. Ovary shallowly 4-lobed; style sub-terminal, stigma lobes subequal to unequal; disc absent. Nutlets obovoid, reticulately ridged, pubescent, abscission-scar lateral, 0.4–0.6× the length of the nutlet.

This new subfamily consists of two small, tropical Asian genera: Acrymia (1 sp., Peninsular Malaysia) and Cymaria (2–3 spp., Hainan, Indo-China and Malesia)(species numbers and ranges from Harley et al.16). The two genera have been included in subfamily Ajugoideae2,59,96,97 or treated as incertae sedis16. A probable synapomorphy of Cymarioideae is its inflorescence structure: the cymes are axillary, lax, and long-pedunculate, with secund, monochasial branches16. This form of inflorescence is rare in the family but also occurs in Garrettia, where it apparently evolved independently.

When describing Cymarioideae, we realized that the type genus of the new subfamily, Cymaria, is currently without a type species. Bentham98 simultaneously named two species, C. dichotoma Benth. and C. elongata Benth., at the same time he described the genus, but he did not designate either as the type. Cymaria was recognized by several subsequent authors, and the two species were always listed in parallel without any type designation1,2,97,99. We take this opportunity to designate C. dichotoma as the type species for Cymaria, because it is more widely distributed and better represented in herbaria.

Lamioideae Harley

The largely Old World subfamily Lamioideae is second in size only to Nepetoideae with over 60 genera and ca. 1200 species. Tribe Stachydeae is cosmopolitan in distribution, and Synandreae is endemic to North America. The other eight tribes are largely Eurasian, but four of them include some African species, and Pogostemon also occurs in Australia16,21,23. All Lamioideae have a gynobasic style, a synapomorphy that arose independently in Nepetoideae and Scutellarioideae9,10. Another possible synapomorphy is the presence of seed oils with an allenic component present4, but this character has been studied in too few species to be fully evaluated. Recent phylogenetic studies based on cpDNA sequence data have identified ten clades that have been ranked as tribes, with several genera unassigned to tribe21,23, but the monophyly of some of these tribes is not supported by nuclear DNA (PPR) data26. Further studies of relationships within some tribes (Synandreae—Scheen et al.29; Roy et al.33; Leucadeae—Scheen and Albert100; Phlomideae—Pan et al.52; Mathiesen et al.101; Salmaki et al.30; Lamieae—Bendiksby et al.102; Stachydeae—Salmaki et al.31; Gomphostemmateae—Xiang et al.53) have led to changes in the composition of some genera, acceptance of genera not recognized by Harley et al.16, and elimination of some genera that were recognized by Harley et al.16. In addition, Chen et al.25 showed that the formerly unplaced genus Holocheila belongs in Lamioideae. Besides Holocheila, four genera have been added to Lamioideae since 2004: Rydingia Scheen & V. A. Albert103, Betonica L.21, Acanthoprasium (Benth.) Spenn.23, and Phlomoides Moench101. Six genera recognized by Harley et al.16 are no longer recognized: Alajja Ikonn. (included in Eriophyton Benth.)23, Sulaimania Hedge & Rech. f. (included in Moluccella L.)23, Pseudoeremostachys Popov and Lamiophlomis Kudo (included in Phlomoides)52,101, Bostrychanthera Benth. (included in Chelonopsis Miq.)102, and Stachyopsis Popov & Vved. (included in Eriophyton Benth.)104. As a result of these changes, Lamioideae is now considered to have 62 genera (versus 63 recognized by Harley et al.16).

Phylogenetic Nomenclature

Our analyses revealed five strongly supported but previously unnamed clades that contain subfamilies (labeled in Fig. 1). These clades warrant naming to facilitate communication about them, but there is no standard rank between family and subfamily. We therefore have given them unranked names, which are defined below, following the rules and recommendations of the draft PhyloCode105. For readers unfamiliar with phylogenetic nomenclature, the preface of the draft PhyloCode provides a good introduction (https://www.ohio.edu/phylocode/preface.html). The names of a variety of plant clades have been defined following the draft PhyloCode, including a set of major tracheophyte and angiosperm clades106, but there have been few previous applications of phylogenetic nomenclature to Lamiaceae. Cantino et al.56 provided phylogenetic definitions for some clade names within Lamiaceae to illustrate differences between phylogenetic and traditional nomenclature, but the PhyloCode did not yet exist, and the names and definitions in that paper were not intended to have any formal nomenclatural status. Salmaki et al.31 phylogenetically defined the name Eurystachys to accommodate the clade comprising the paraphyletic genus Stachys and ten other genera that nest within it. Phylogenetic definitions for the names Labiatae and Nepetoideae have been prepared by P. D. Cantino & R. G. Olmstead and will be published in Phylonyms (de Queiroz et al., in prep.).

Cymalamiina B. Li, R. G. Olmstead & P. D. Cantino, new clade name


The smallest crown clade containing Lamium purpureum L. 1753 and Cymaria dichotoma Benth. 1930.

Primary reference phylogeny

Figure 2; see also Fig. 1 (this paper), Bendiksby et al.23 (Fig. 1), Chen et al.25 (Fig. 4), Roy and Lind qvist26 (Fig. 1a), and Chen et al.43 (Fig. 3, where Cymaria represents Cymarioideae).


Cymarioideae and Lamioideae.


Confluent anther thecae may be a synapomorphy. It is shared by Cymarioideae and one of the two basal subclades of Lamioideae (i.e., Pogostemoneae), but the anthers in the other basal subclade (i.e., the rest of Lamioideae) vary from distinct (e.g., Gomphostemmateae, Synandreae, Galeopsis L.) to confluent (e.g., Colquhounia Wall. and some Stachydeae). The closest outgroups to Cymalamiina (i.e., Scutellarioideae and Peronematoideae) have distinct thecae (except Garrettia in Peronematoideae), as do the more distant outgroups Premnoideae and Tectona; this character varies in Ajugoideae, another more distant outgroup. Given the distribution of the character states and its variability within many tribes of Lamioideae, it is not clear whether confluent thecae is a synapomorphy of Cymalamiina with a series of reversals within Lamioideae or, alternatively, that it evolved independently in Cymarioideae, Pogostemoneae, and in scattered other members of Lamioideae.

Scutelamiina B. Li, R. G. Olmstead & P. D. Cantino, new clade name


The smallest crown clade containing Lamium purpureum L. 1753 and Scutellaria galericulata L. 1753.

Primary reference phylogeny

Figure 2; see also Fig. 1 (this paper), Bendiksby et al.23 (Fig. 1), Chen et al.25 (Fig. 4), and Chen et al.43 (Fig. 3).


Scutellarioideae, Cymarioideae and Lamioideae.


A four-lobed ovary appears to be a synapomorphy for Scutelamiina. It is shallowly four lobed in Cymarioideae and the more basal members of Scutellarioideae (though unlobed in Holmskioldia) and deeply lobed in Lamioideae and Scutellaria. A developmentally related feature, a schizocarpic fruit with four mericarps (“nutlets”), may be another synapomorphy of Scutelamiina. However, within its sister group (Peronematoideae), the 4-seeded capsule of Garrettia and Peronema breaks with pressure into four mericarps, possibly representing a stage in the evolution of the schizocarp of Scutelamiina. Another likely synapomorphy is suprareticulate (sometimes called bireticulate) pollen, which is found in all genera of Scutellarioideae and Cymarioideae and most genera of Lamioideae90,107,108,109. However the presence of suprareticulate pollen in Garrettia (Peronematoideae)90,110 and suprarugulose pollen in Peronema110 raises the possibility that this feature may be a synapomorphy for Perolamiina rather than Scutelamiina, though Petraeovitex and Hymenopyramis (the more distal genera within Peronematoideae) have psilate pollen110. Furthermore, suprareticulate sculpturing could be synapomorphic at an even more inclusive level because it occurs in some genera of Premnoideae (Gmelina, but not Cornutia or Premna, based on very few species90,110).


Cantino et al.56 applied the name Lamiina to this clade and provided a phylogenetic definition, but the names used in that paper were intended only to illustrate differences between phylogenetic and traditional rank-based nomenclature. They were not intended to have nomenclatural precedence under either system, and the PhyloCode did not yet exist.

Perolamiina B. Li, R. G. Olmstead & P. D. Cantino, new clade name


The smallest crown clade containing Lamium purpureum L. 1753 and Peronema canescens Jack 1822.

Primary reference phylogeny

Figure 2; see also Fig. 1 (this paper), Bendiksby et al.23 (Fig. 1, where Garrettia represents Peronematoideae), Chen et al.25 (Fig. 4, where Garrettia, Hymenopyramis and Petraeovitex represent Peronematoideae), and Chen et al.43 (Fig. 3, where Hymenopyramis, Petraeovitex and Peronema represent Peronematoideae).


Peronematoideae, Scutellarioideae, Cymarioideae and Lamioideae.


Supareticulate pollen may be a synapomorphy; see Scutelamiina.

Viticisymphorina B. Li, R. G. Olmstead & P. D. Cantino, new clade name


The smallest crown clade containing Vitex agnus-castus L. 1753 and Symphorema involucratum Roxb. 1805 but not Nepeta cataria L. 1753, Tectona grandis L. f. 1782, Premna serratifolia L. 1771, Ajuga reptans L. 1753, and Lamium purpureum L. 1753.

Primary reference phylogeny

Figure 3; see also Fig. 1 (this paper), Bendiksby et al.23 (Fig. 1, where Congea represents Symphorematoideae, Vitex and Petitia represent Viticoideae), and Bramley et al.47 (Fig. 1, where Sphenodesme represent Symphorematoideae).


Viticoideae and Symphorematoideae.


No non-molecular synapomorphies are known.


We intend this name to be applicable only if Symphorematoideae and Viticoideae are sister groups. Although our analyses strongly support the monophyly of this grouping, it is not supported in some other analyses24,25,43. For this reason, the definition includes external specifiers to make the name inapplicable under many alternative phylogenies.

Calliprostantherina B. Li, R. G. Olmstead & P. D. Cantino, new clade name


The smallest crown clade containing Callicarpa americana L. 1753 and Prostanthera lasianthos Labillardiére 1806, but not Vitex agnus-castus L. 1753, Nepeta cataria L. 1753, Tectona grandis L. f. 1782, Premna serratifolia L. 1771, Ajuga reptans L. 1753, and Lamium purpureum L. 1753.

Primary reference phylogeny

Figure 3; see also Fig. 1 (this paper), Olmstead et al.20 (Fig. 1), Refulio-Rodriguez and Olmstead15 (Fig. 1A, where Prostanthera represents Prostantheroideae), and Chen et al.43 (Fig. 3, where Prostanthera and Westringia represent Prostantheroideae).


Callicarpa and Prostantheroideae.


Branched trichomes and actinomorphic corollas, two characters that are infrequent in Lamiaceae, are shared by Callicarpa and Chloantheae (one of the two basal subclades of Prostantheroideae). Branched trichomes also occur in scattered species of the other subclade (Westringieae), increasing the likelihood that this feature characterizes Calliprostantherina. However, it could be apomorphic at a deeper level in the phylogeny since Symphorematoideae and Tectona also have branched hairs (see Fig. 1 for the relationship of the latter taxa to Calliprostantherina). Actinomorphic corollas also occur in Tectona and some genera of Symphorematoideae; furthermore, all species of Westringieae have zygomorphic flowers, weakening the hypothesis that actinomorphy is a synapomorphy for Calliprostantherina. There are similarities in pollen surface sculpturing between some species of Callicarpa and some genera of Prostantheroideae111, but there is considerable variation in both groups, and the polarity of the character is unknown.


Because the molecular support for this clade is only moderate and the potential morphological synapomorphies discussed above are not convincing, the definition is designed to become inapplicable under many alternative phylogenies (e.g., Bendiksby et al.23: Fig. 1).

Type designation and new combinations

Cymaria Bentham in Edwards’s Bot. Reg. 15: t. 1292. 1830. Type (here designated): Cymaria dichotoma Bentham in Edwards’ Bot. Reg. 15: t. 1292. 1830.

Vitex petitia Bramley, nom. nov

Bas.: Petitia domingensis Jacq. in Enum. Syst. Pl.: 12. 1760.—Lectotype (here designated): Haiti, Jacquin s.n. (BM! fragment, barcode no. BM000992805).

Note:—A new name rather than a new combination has been created for Petitia domingensis, since the name Vitex domingensis Urb. & Ekman already exists (=Pseudocarpidium domingense (Urb. & Ekman) Moldenke). The epithet ‘petitia’ has been chosen to retain an obvious link to the original name of the species, which is quite common across the West Indies. The fragment of Jacquin’s specimen housed at the BM has been designated as lectotype, as suggested by annotation on the sheet by H. N. Moldenke according to d’Arcy112. Jacquin’s herbarium was reportedly bought by Banks and incorporated into his collections.

Vitex urbanii (Ekman) Bramley, comb. nov

Bas.: Petitia urbanii Ekman in Ark. Bot. 21A(5): 94. 1927. —Lectotype (here designated): Haiti, Ile de la Tortue, steep limestone rocks west of Monillago Anglais, 22 May 1925, E. L. Ekman H4096 (S! sheet number S04-2601; isolectotypes A!, B, F!, G!, K!, NY!, S!, UC!, US!).

Note:—One of the sheets at S [sheet number S04-2601] is designated as lectotype because E. L. Ekman was based there, and it has attached to it a handwritten note “it is a pleasure to dedicate this fine new species to Prof. Urban, the admirable botanist, the never tiring worker, and the best friend a man ever had”.

Materials and Methods

Choice of markers, taxon sampling and molecular data

Five chloroplast DNA markers—matK, ndhF, rbcL, rps16, and trnL-F—were employed in this study because (1) they have been widely used in phylogenetic reconstructions of Lamiaceae at generic, tribal or subfamilial level, and (2) many species of Lamiaceae have already been sequenced for these markers in previous molecular studies9,10,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,101. No comparable source of data exists for any nuclear DNA region for a broad sample of Lamiaceae.

The ingroup sample included representatives of all seven subfamilies and all ten genera incertae sedis recognized by Harley et al.16 and all 14 tribes recognized by Olmstead18. Nomenclature of Lamiaceae and Viticoideae s. str. followed Olmstead18 and Bramley et al.47, respectively. Initially, we downloaded data for all taxa of Lamiaceae with sequence information for any of the five gene regions deposited in Genbank as of August 2015. In the five subfamilies whose monophyly is well supported (viz., Ajugoideae, Lamioideae, Nepetoideae, Prostantheroideae and Scutellarioideae), sampling was designed to cover their genus-level diversity. Generally, genera with at least two sequenced regions were selected, and each selected genus was represented by one or two species. Particular emphasis was placed on sampling Symphorematoideae, Viticoideae s. str., all genera incertae sedis, and three genera formerly assigned to Viticoideae—Cornutia, Gmelina, and Premna. In three large genera—Callicarpa, Premna, and Vitex, sampling was designed to cover their morphological and geographic breadth. In total, 288 species representing 191 genera were included, representing approximately 78% of the genera of Lamiaceae. Five outgroup species were selected representing the closest relatives to Lamiaceae in Lamiales12,13,14,15. They are Lindenbergia philippensis (Cham. & Schltdl.) Benth. and Pedicularis groenlandica Retz. from Orobanchaceae, Paulownia tomentosa (Thunb.) Steud. from Paulowniaceae, Mazus reptans N. E. Br. from Mazaceae and Phryma leptostachya L. from Phrymaceae. Information on sampled taxa and Genbank accession numbers is assembled in Supplementary Table S1.

The five separate molecular data sets matK, ndhF, rbcL, rps16 and trnL-F contained 202, 160, 170, 181, and 259 sequences with 54, 83, 59, 57, and 88 newly reported sequences, respectively. The dataset combining the five markers included 270 taxa (D270), with 39.65 % missing data. According to investigations by Wiens113 and Wiens and Moen114, the proportion of missing data should not affect the accuracy of the phylogenetic analysis; however, just to make sure, a reduced dataset was assembled including 155 taxa (D155) with at least three of the five regions or 50 % of the total aligned sequence length available for each terminal taxon. The total amount of missing data in D155 was 23.51 %. For most species in the combined datasets, data were available for all five regions, but there were some genera of Ajugoideae, Lamioideae, Nepetoideae, Prostantheroideae, and Scutellarioideae in which different species were used for different gene regions. When data were pooled in this way, generic names, rather than species names, were used to represent the combined sequences in the phylogenetic trees.

DNA extraction, amplification, and sequencing

The 2x CTAB method of Doyle and Doyle115 was used to extract total genomic DNA of the samples with silica dried leaf tissue, and DNEasy® Plant Mini Kit (QIAGEN®, Valencia, California, USA) was used for herbarium materials according to the manufacturer’s specifications. The DNA extracts were dissolved in TE buffer and preserved at −20 °C for further use.

Primer pairs used in Polymerase chain reaction (PCR) amplification of the five regions are listed in Table S2 with their sequences and references. The PCR reaction system and amplification protocol were identical for all five fragments. PCR reactions used 2.5 μL sample DNA, 0.5 μL Dream Taq DNA polymerase, 5 μL 10 × DreamTaq Green Buffer, 5 μL dNTP Mix (2 mM each), 1 μL of bovine serum albumin (BSA, 20 mg/mL), 1 μL of each primer in a final reaction volume of 50 μL. The PCR program was as follows: an initial template denaturation at 94 °C for 5 min, 35 cycles of 30 second denaturation at 94 °C, 1 minute primer annealing at 52 °C, 1.5 min extension at 72 °C, with a final extension of 8 min at 72 °C. Sequencing was done by the Invitrogen sequencing service (Invitrogen, commercial sequencing facility, Guangzhou, China) using the same primers for PCR amplifications.

Sequence alignment and phylogenetic analyses

Sequencher v.4.5116 was used to evaluate chromatograms for base confirmation and to edit contiguous sequences. All DNA sequences were initially aligned using Clustal X v.2.0.117 and adjusted manually in BioEdit Sequence Alignment Editor v.7.0.0118.

The separate data sets were first analyzed using Maximum parsimony (MP) and Maximum likelihood (ML) methods, with gaps treated as simple indels determined by the program Gapcoder119 and added to the matrix as binary presence/absence characters. The combined data sets D270 and D155 were analyzed using MP, ML and Bayesian inference (BI) methods with gaps treated either as missing data or as simple indels.

MP analyses were conducted using PAUP* v.4.0b10120 with all characters unordered and equally weighted. Heuristic search was conducted using 1000 random addition sequence replicates, tree-bisection-reconnection (TBR) branch swapping, MulTrees in effect, and steepest descent off. Bootstrap support values (BS) were estimated using a heuristic search strategy with 500 bootstrap replicates and 1000 random sequences additions.

ML analyses were performed on the web server RAxML Black Box121. Before each submission, the “Maximum likelihood search” and “Estimate proportion ofinvariable sites” options were selected, with a total of 1000 bootstrap replicates performed.

BI analysis was executed using MrBayes version 3.2.2122 on the CIPRES Science Gateway123 with the default parameters. The best substitution types (Nst) and rate distribution models (rates) were determined by the Akaike information criterion (AIC) using Model Test v.3.7124 with the hierarchical likelihood ratio tests. Four Markov chain Monte Carlo (MCMC) chains were run, each beginning with a random tree and sampling one tree every 1000 generations for 30 000 000 generations. Mixing, convergence and a suitable burn-in were assessed with the statistics provided by the program and with Tracer v. 1.6125. Post burn-in samples from the four runs were merged using LogCombiner v1.7.5. (available at http://beast.bio.ed.ac.uk/, LogCombiner) prior to the calculation of a 50 % majority-rule consensus tree.

Additional Information

How to cite this article: Li, B. et al. A large-scale chloroplast phylogeny of the Lamiaceae sheds new light on its subfamilial classification. Sci. Rep. 6, 34343; doi: 10.1038/srep34343 (2016).


  1. 1

    Bentham, G. In Genera plantarum, Vol. 2 (eds Bentham, G. & Hooker, J. D. ), Verbenaceae and Labiatae, 1131–1223 (Reeve, London, 1876).

    Google Scholar 

  2. 2

    Briquet, J. In Die natürlichen Pflanzenfamilien, Vol. 4 (3a)(eds Engler, A. & Prantl, K. ), Labiatae, 183–375 (Engelmann, Leipzig, 1895–1897).

    Google Scholar 

  3. 3

    Briquet, J. In Die natürlichen Pflanzenfamilien, Vol. 4 (3a) (eds Engler, A. & Prantl, K. ), Verbenaceae, 132–182 (Engelmann, Leipzig, 1895).

    Google Scholar 

  4. 4

    Cantino, P. D. In Advances in Labiate science (eds Harley, R. M. & Reynolds, T. ), Toward a phylogenetic classification of the Labiatae, 27–37 (Royal Botanic Gardens, Kew, London, 1992).

  5. 5

    Junell, S. Zur Gynaceum morphologie und Systematik der Verbenaceen und Labiaten. Symb. Bot. Upsal. 4, 1–219 (1934).

    Google Scholar 

  6. 6

    Abu-Asab, M. S. Phylogenetic implications of pollen morphology in subfamily Lamioideae (Labiatae) and related taxa (Ph.D. Thesis) (Ohio University, USA, 1990).

  7. 7

    Abu-Asab, M. S. & Cantino, P. D. In Advances in Labiate science (eds Harley, R. M. & Reynolds, T. ), Pollen morphology in subfamily Lamioideae (Labiatae) and its phylogenetic implications, 97–112 (Royal Botanic Gardens, Kew, London, 1992).

  8. 8

    Cantino, P. D. Evidence for a polyphyletic origin of the Labiatae. Ann. Missouri Bot. Gard. 79, 361–379 (1992).

    Article  Google Scholar 

  9. 9

    Wagstaff, S. J. & Olmstead, R. G. Phylogeny of Lamiaceae and Verbenaceae inferred from rbcL sequences. Syst. Bot. 22, 165–179 (1997).

    Article  Google Scholar 

  10. 10

    Wagstaff, S. J., Hickerson, L., Spangler, R., Reeves, P. A. & Olmstead, R. G. Phylogeny of Lamiaceae s. l. inferred from cpDNA sequences. Plant Syst. Evol. 209, 265–274 (1998).

    Article  CAS  Google Scholar 

  11. 11

    Cronquist, A. An integrated system of classification of flowering plants. (Columbia University Press, New York, 1981).

  12. 12

    Oxelman, B., Kornhall, P., Olmstead, R. G. & Bremer, B. Further disintegration of Scrophulariaceae. Taxon 54, 411–425 (2005).

    Article  Google Scholar 

  13. 13

    Schäferhoff, B. et al. Towards resolving Lamiales relationships: insights from rapidly evolving chloroplast sequences. BMC Evol. Biol. 10, 352 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. 14

    Perret, M., Chautems, A., De Araujo, A. O. & Salamin, N. Temporal and spatial origin of Gesneriaceae in the New World inferred from plastid DNA sequences. Bot. J. Linn. Soc. 171, 61–79 (2013).

    Article  Google Scholar 

  15. 15

    Refulio-Rodriguez, N. F. & Olmstead, R. G. Phylogeny of Lamiidae. Am. J. Bot. 101, 287–299 (2014).

    Article  PubMed  Google Scholar 

  16. 16

    Harley, R. M. et al. In Families and genera of vascular plants, Vol. 7 (eds Kubitzki, K. & Kadereit, J. W. ), Labiatae, 167–275 (Springer, Berlin, 2004).

    Google Scholar 

  17. 17

    The Angiosperm Phylogeny Group. An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG IV. Bot. J. Linn. Soc. 181, 1–20 (2016).

  18. 18

    Olmstead, R. G. A synoptical classification of the Lamiales, version 2.4 (2012) Available at: http://depts.washington.edu/phylo/Classification.pdf. (Accessed: 5th April 2013).

  19. 19

    Soltis, D. E. et al. Angiosperm phylogeny: 17-genes, 640 taxa. Am. J. Bot. 98, 704–730 (2011).

    Article  PubMed  Google Scholar 

  20. 20

    Olmstead, R. G., Reeves, P. A. & Lepschi, B. J. Confirmation of a monophyletic Chloanthoideae (Lamiaceae) comprising tribes Chloantheae and Prostanthereae. Lamiales Newsletter 6, 7–10 (1998).

    Google Scholar 

  21. 21

    Scheen, A. C. et al. Molecular phylogenetics, character evolution, and suprageneric classification of Lamioideae (Lamiaceae). Ann. Missouri Bot. Gard. 97, 191–217 (2010).

    Article  Google Scholar 

  22. 22

    Yuan, Y. W., Mabberley, D. J., Steane, D. A. & Olmstead, R. G. Further disintegration and redefinition of Clerodendrum (Lamiaceae): implications for the understanding of the evolution of an intriguing breeding strategy. Taxon 59, 125–133 (2010).

    Article  Google Scholar 

  23. 23

    Bendiksby, M., Thorbek, L., Scheen, A. C., Lindqvist, C. & Ryding, O. An updated phylogeny and classification of Lamiaceae subfamily Lamioideae. Taxon 60, 471–484 (2011).

    Article  Google Scholar 

  24. 24

    Li, B. et al. Phylogenetic position of Wenchengia (Lamiaceae): a taxonomicallyenigmatic and critically endangered genus. Taxon 61, 392–401 (2012).

    Article  Google Scholar 

  25. 25

    Chen, Y. P. et al. Phylogenetic placement of the enigmatic genus Holocheila (Lamiaceae) inferred from plastid DNA sequences. Taxon 63, 355–366 (2014).

    Article  Google Scholar 

  26. 26

    Roy, T. & Lindqvist, C. New insights into evolutionary relationships within the subfamily Lamioideae (Lamiaceae) based on pentatricopeptide repeat (PPR) nuclear DNA sequences. Amer. J. Bot. 102, 1721–1735 (2015).

    Article  CAS  Google Scholar 

  27. 27

    Steane, D. A., de Kok, R. P. & Olmstead, R. G. Phylogenetic relationships between Clerodendrum (Lamiaceae) and other Ajugoid genera inferred from nuclear and chloroplast DNA sequence data. Mol. Phylogenet. Evol. 32, 39–45 (2004).

    Article  CAS  PubMed  Google Scholar 

  28. 28

    Lindqvist, C. & Albert, V. A. Origin of the Hawaiian endemic mints within North American Stachys (Lamiaceae). Am. J. Bot. 89, 1709–1724 (2002).

    Article  PubMed  Google Scholar 

  29. 29

    Scheen, A. C., Lindqvist, C., Fossdal, C. G. & Albert, V. A. Molecular phylogenetics of tribe Synandreae, a North American lineage of lamioid mints (Lamiaceae). Cladistics 24, 299–314 (2008).

    Article  Google Scholar 

  30. 30

    Salmaki, Y. et al. Phylogeny of the tribe Phlomideae (Lamioideae: Lamiaceae) with special focus on Eremostachys and Phlomoides: new insights from nuclear and chloroplast sequences. Taxon 61, 161–179 (2012).

    Article  Google Scholar 

  31. 31

    Salmaki, Y. et al. Molecular phylogeny of tribe Stachydeae (Lamiaceae subfamily Lamioideae). Mol. Phylogenet. Evol. 69, 535–551 (2013).

    Article  PubMed  Google Scholar 

  32. 32

    Roy, T., Chang, T. H., Lan, T. Y. & Lindqvist, C. Phylogeny and biogeography of New World Stachydeae (Lamiaceae) with emphasis on the origin and diversification of Hawaiian and South American taxa. Mol. Phylogenet. Evol. 69, 218–238 (2013).

    Article  CAS  PubMed  Google Scholar 

  33. 33

    Roy, T. et al. Evolutionary relationships within the lamioid tribe Synandreae (Lamiaceae) based on multiple low-copy nuclear loci. PeerJ PrePrints 4, e1725v1 (2016).

    Google Scholar 

  34. 34

    Paton, A. J. et al. Phylogeny and evolution of basils and allies (Ocimeae, Labiatae) based on three plastid DNA regions. Mol. Phylogenet. Evol. 31, 277–299 (2004).

    Article  CAS  PubMed  Google Scholar 

  35. 35

    Walker, J. B., Sytsma, K. J., Treutlein, J. & Wink, M. Salvia (Lamiaceae) is not monophyletic: implications for the systematics, radiation, and ecological specializations of Salvia and tribe Mentheae. Am. J. Bot. 91, 1115–1125 (2004).

    Article  PubMed  Google Scholar 

  36. 36

    Walker, J. B. & Sytsma, K. J. Staminal evolution in the genus Salvia (Lamiaceae): molecular phylogenetic evidence for multiple origins of the staminal lever. Ann. Bot. 100, 375–391 (2007).

    Article  CAS  PubMed  Google Scholar 

  37. 37

    Bräuchler, C., Meimberg, H. & Heubl, G. Molecular phylogeny of Menthinae (Lamiaceae, Nepetoideae, Mentheae)–taxonomy, biogeography and conflicts. Mol. Phylogenet. Evol. 55, 501–523 (2010).

    Article  CAS  PubMed  Google Scholar 

  38. 38

    Moon, H. K., Smets, E. & Huysmans, S. Phylogeny of tribe Mentheae (Lamiaceae): the story of molecules and micromorphological characters. Taxon 59, 1065–1076 (2010).

    Article  Google Scholar 

  39. 39

    Drew, B. T. & Sytsma, K. J. Testing the monophyly and placement of Lepechinia in the tribe Mentheae (Lamiaceae). Syst. Bot. 36, 1038–1049 (2011).

    Article  Google Scholar 

  40. 40

    Drew, B. T. & Sytsma, K. J. Phylogenetics, biogeography, and staminal evolution in the tribe Mentheae (Lamiaceae). Am. J. Bot. 99, 933–953 (2012).

    Article  PubMed  Google Scholar 

  41. 41

    Drew, B. T. & Sytsma, K. J. The South American radiation of Lepechinia (Lamiaceae): phylogenetics, divergence times and evolution of dioecy. Bot. J. Linn. Soc. 171, 171–190 (2013).

    Article  Google Scholar 

  42. 42

    Drew, B. T., Cacho, N. I. & Sytsma, K. J. The transfer of two rare monotypic genera, Neoeplingia and Chaunostoma, to Lepechinia (Lamiaceae), and notes on their conservation. Taxon 63, 831–842 (2014).

    Article  Google Scholar 

  43. 43

    Chen, Y. P. et al. Resolving the phylogenetic position of Ombrocharis (Lamiaceae), with reference to the molecular phylogeny of tribe Elsholtzieae. Taxon 65, 123–136 (2016).

    Article  Google Scholar 

  44. 44

    Guerin, G. R. Evidence for polyphyly in Hemigenia and Microcorys (Lamiaceae: Westringieae). Aust . Syst. Bot. 21, 313–325 (2008).

    Article  Google Scholar 

  45. 45

    Conn, B. J., Streiber, N., Brown, E. A., Henwood, M. J. & Olmstead, R. G. Infrageneric phylogeny of Chloantheae (Lamiaceae) based on chloroplast ndhF and nuclear ITS sequence data. Aust . Syst. Bot. 22, 243–256 (2009).

    Article  Google Scholar 

  46. 46

    Wilson, T. C., Conn, B. J. & Henwood, M. J. Molecular phylogeny and systematics of Prostanthera (Lamiaceae). Aust. Syst. Bot. 25, 341–352 (2012).

    Article  Google Scholar 

  47. 47

    Bramley, G. L. C., Forest, F. & De Kok, R. P. J. Troublesome tropical mints: re-examining generic limits of Vitex and relations (Lamiaceae) in South East Asia. Taxon 58, 500–510 (2009).

    Article  Google Scholar 

  48. 48

    Olmstead, R. G. A synoptical classification of the Lamiales, version 2.2. (2010) Available at: http://my-plant.org/sites/default/files/lamiales_classn.v.2.2_0.pdf. (Accessed: 20 November 2012).

  49. 49

    Bramley, G. L. C. The genus Callicarpa (Lamiaceae) on Borneo. Bot. J. Linn. Soc. 159, 416–455 (2009).

    Article  Google Scholar 

  50. 50

    Zhong, J. S., Li, J., Li, L., Conran, J. G. & Li, H. W. Phylogeny of Isodon (Schrad. ex Benth.) Spach (Lamiaceae) and related genera inferred from nuclear ribosomal ITS, trnL-trnF region, and rps16 intron sequences and morphology. Syst. Bot. 35, 207–219 (2010).

    Article  Google Scholar 

  51. 51

    Huang, M., Crawford, D. J., Freudenstein, J. V. & Cantino, P. D. Systematics of Trichostema (Lamiaceae): evidence from ITS, ndhF, and morphology. Syst. Bot. 33, 437–446 (2008).

    Article  Google Scholar 

  52. 52

    Pan, Y. Z., Fang, L. Q., Hao, G., Cai, J. & Gong, X. Systematic positions of Lamiophlomis and Paraphlomis (Lamiaceae) based on nuclear and chloroplast sequences. J. Syst. Evol. 47, 535–542 (2009).

    Article  Google Scholar 

  53. 53

    Xiang, C. L. et al. Molecular phylogenetics of Chelonopsis (Lamiaceae: Gomphostemmateae) as inferred from nuclear and plastid DNA and morphology. Taxon 62, 375–386 (2013).

    Article  Google Scholar 

  54. 54

    Hillis, D. M. Taxonomic sampling, phylogenetic accuracy, and investigator bias. Syst. Biol. 47, 3–8 (1998).

    Article  CAS  PubMed  Google Scholar 

  55. 55

    Heath, T. A., Hedtke, S. M. & Hillis, D. M. Taxon sampling and the accuracy of phylogenetic analyses. J. Syst. Evol. 46, 239–257 (2008).

    Google Scholar 

  56. 56

    Cantino, P. D., Olmstead, R. G. & Wagstaff, S. J. A comparison of phylogenetic nomenclature with the current system: a botanical case study. Syst. Biol. 46, 313–331 (1997).

    Article  Google Scholar 

  57. 57

    Hutchinson, J. The families of flowering plants 2nd ed, Vol. 1 (Oxford University Press, London, 1959).

  58. 58

    Munir, A. A. A taxonomic revision of the genus Chloanthes (Chloanthaceae). J. Adelaide Bot. Gard. 1, 83–106 (1977).

    Google Scholar 

  59. 59

    Cantino, P. D., Harley, R. M. & Wagstaff, S. J. In Advances in Labiate science (eds Harley, R. M. & Reynolds, T. ), Genera of Labiatae: status and classification, 511–522 (Royal Botanic Gardens, Kew, London, 1992).

  60. 60

    Munir, A. A. A taxonomic revision of the genus Spartothamnella (Chloanthaceae). J. Adelaide Bot. Gard. 1, 3–25 (1976).

    Google Scholar 

  61. 61

    Wilson, T. C., Henwood, M. J. & Conn, B. J. Status of the genus Wrixonia F. Muell. (Lamiaceae). Telopea 14, 1–3 (2012).

    Article  Google Scholar 

  62. 62

    Rye, B. L. A taxonomic review of Dicrastylis sect. Corymbosae (Lamiaceae: Chloantheae), incorporating Mallophora as a new synonym. Nuytsia 15, 445–455 (2005).

    Google Scholar 

  63. 63

    Conn, B. J., Henwood, M. J. & Streiber, N. Synopsis of the tribe Chloantheae and new nomenclatural combinations in Pityrodias. lat. (Lamiaceae). Aust . Syst. Bot. 24, 1–9 (2011).

    Article  Google Scholar 

  64. 64

    Guerin, G. R. A taxonomic revision of Hemigenia section Malleantha sect. nov. (Lamiaceae: Westringieae). Aust . Syst. Bot. 21, 326–374 (2008).

    Article  Google Scholar 

  65. 65

    Pedersen, J. A. Distribution and taxonomic implications of some phenolics in the family Lamiaceae determined by ESR spectroscopy. Biochem. Syst. Ecol. 28, 229–253 (2000).

    Article  CAS  Google Scholar 

  66. 66

    Koorders, S. H. Teijsmanniodendron, eine neue Gattung der Verbanaceae im Botanischen Garten von Buitenzorg. Ann. Jard. Bot. Buitenzorg 19, 19–31 (1904).

    Google Scholar 

  67. 67

    Callmander, M. W., Philipson, P. B. & Schatz, G. E. Towards a revision of the genus Vitex L. (Lamiaceae) in Madagascar I: a distinctive new species from North-eastern Madagascar. Candollea 69, 141–147 (2014).

    Article  Google Scholar 

  68. 68

    Cantino, P. D. & Sanders, R. W. Subfamilial classification of Labiatae. Syst. Bot. 11, 163–185 (1986).

    Article  Google Scholar 

  69. 69

    Erdtman, G. Pollen morphology and plant taxonomy IV: Labiatae, Verbenaceae and Avicenniaceae. Svensk Bot. Tidskr. 39, 279–285 (1945).

    Google Scholar 

  70. 70

    Ryding, O. In Advances in Labiate Science (eds. Harley, R. M. & Reynolds, T. ), The distribution and evolution of myxocarpy in Lamiaceae, 85–96 (Royal Botanic Gardens, Kew, London, 1992).

  71. 71

    Wunderlich, R. Ein Vorschlag zu einer natürlichen Gliederung der. Labiaten. Oesterr. Bot. Z. 114, 383–483 (1967).

    Article  Google Scholar 

  72. 72

    Bräeuchler, C., Doroszenko, A., Esser, H. J. & Heubl, G. Killickia (Lamiaceae): a new genus from KwaZulu-Natal, South Africa. Bot. J. Linn. Soc. 157, 575–586 (2008).

    Article  Google Scholar 

  73. 73

    Harley, R. M. & Pastore, J. F. B. A generic revision and new combinations in the Hyptidinae (Lamiaceae), based on molecular and morphological evidence. Phytotaxa 58, 1–55 (2012).

    Article  Google Scholar 

  74. 74

    Deng, T. et al. Does the Arcto-Tertiary biogeographic hypothesis explain the disjunct distribution of northern hermisphere herbaceous plants? The case of Meehania (Lamiaceae). PLoS ONE 10, e0117171 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  75. 75

    Verdcourt, B. In Flora of tropical east Africa (ed. Polhill, R. M. ), Verbenaceae, 1–156 (Balkema, Rotterdam, 1992).

  76. 76

    Mabberley, D. J. Mabberley’s Plant-Book: a Portable Dictionary of Plants, 3rd ed. (Cambridge University Press, Cambridge, 2008).

  77. 77

    Munir, A. A. A taxonomic revision of the genus Premna L. (Verbenaceae) in Australia. J. Adelaide Bot. Gard. 7, 1–44 (1984).

    Google Scholar 

  78. 78

    Chen, S. L. & Gilbert, M. G. In Flora of China, Vol. 17 (eds Wu, C. Y. & Raven, P. H. ), Verbenaceae, 1–49 (Science Press, Beijing & Missouri Botanical Garden Press, St. Louis, 1994).

    Google Scholar 

  79. 79

    Rajendran, A. & Daniel, P. The Indian Verbenaceae (Shiva Press, Dehra Dun, 2002).

  80. 80

    Mabberley, D. J. & de Kok, R. P. J. In Flore de la Nouvelle-Calédonieet Dépendances, Vol. 25 (eds Morat, P. & Mackee, H. S. ), Labiatae, 20–141 (Muséum National D’Histoire Naturelle, Paris, 2005).

    Google Scholar 

  81. 81

    Leeratiwong, C., Chantaranothai, P. & Paton, A. A synopsis of the genus Premna L. (Lamiaceae) in Thailand. Nat. Hist. J. Chulalongkorn Univ. 9, 113–142 (2009).

    Google Scholar 

  82. 82

    De Kok, R. P. J. The genus Premna L. (Lamiaceae) in the Flora Malesiana area. Kew Bull. 68, 55–84 (2013).

    Article  Google Scholar 

  83. 83

    De Kok, R. P. J. A revision of the genus Gmelina (Lamiaceae). Kew Bull. 67, 293–329 (2012).

    Article  Google Scholar 

  84. 84

    Steane, D. A. et al. Phylogenetic relationships of Clerodendrum s. l. (Lamiaceae) inferred from chloroplast DNA. Syst. Bot. 22, 229–244 (1997).

    Article  Google Scholar 

  85. 85

    Steane, D. A., Scotland, R. W., Mabberley, D. J. & Olmstead, R. G. Molecular systematics of Clerodendrum (Lamiaceae): ITS sequences and total evidence. Amer. J. Bot. 86, 98–107 (1999).

    Article  CAS  Google Scholar 

  86. 86

    Cantino, P. D., Wagstaff, S. J. & Olmstead, R. G. Caryopteris (Lamiaceae) and the conflict between phylogenetic and pragmatic considerations in botanical nomenclature. Syst. Bot. 23, 369–386 (1999).

    Article  Google Scholar 

  87. 87

    Huang, M. Systematics of Trichostema L. (Lamiaceae) and phylogenetic relationships with its disjunct taxa in Asia. (Ph.D. Thesis)(Ohio University, USA, 2002).

  88. 88

    Shi, S. H. et al. Phylogenetic position of Schnabelia, a genus endemic to China: evidence from sequences of cpDNA matK gene and nrDNA ITS regions. Chinese Sci. Bull. 48, 1576–1580 (2003).

    Article  ADS  CAS  Google Scholar 

  89. 89

    Barrabe, L. et al. Recircumscription of Oxera (Lamiaceae: Ajugoideae) to include Faradaya based on molecular and anatomical data. Bot. J. Linn. Soc. 179, 693–711 (2015).

    Article  Google Scholar 

  90. 90

    Abu-Asab, M. S. & Cantino, P. D. Phylogenetic implications of pollen morphology in tribe Ajugeae (Labiatae). Syst. Bot. 18, 100–122 (1993).

    Article  Google Scholar 

  91. 91

    Abu-Asab, M. S., Cantino, P. D., Nowicke, J. W. & Sang, T. Systematic implications of pollen morphology in Caryopteris (Labiatae). Syst. Bot. 18, 502–515 (1993).

    Article  Google Scholar 

  92. 92

    Wu, C. Y. In Flora Yunnanica, Vol. 1 (eds. Kunming Institute of Botany, Academia Sinica), Verbenaceae, 390–490 (Science Press, Beijing, 1977).

    Google Scholar 

  93. 93

    P’ei, C. & Chen, S. L. In Flora Reipublicae Popularis Sinicae, Vol. 65 (eds. P’ei, C. & Chen, S. L. ), Verbenaceae, 1–208 (Science Press, Beijing, 1982).

    Google Scholar 

  94. 94

    Paton, A. A global taxoboic investigation of Scutellaria (Labiatae). Kew Bull. 45, 399–450 (1990).

    Article  Google Scholar 

  95. 95

    Ryding, O. Amount of calyx fibers in Lamiaceae, relation to calyx structure, phylogeny and ecology. Plant Syst. Evol. 268, 45–58 (2007).

    Article  Google Scholar 

  96. 96

    Prain, D. Decades Kewenses: XLVII.-XLVIII. Bull. Misc. Inform. Kew 3, 105–116 (1908).

    Google Scholar 

  97. 97

    Keng, H. In Flora Malesiana. Series I, Spermatophyta, Flowering Plants, Vol. 8 (ed. Van Steenis, C. G. G. J. ), Labiatae, 301–394 (Sijthoff & Noordhoff International Publishers, Alphen aan den Rijn, 1978).

    Google Scholar 

  98. 98

    Bentham, G. In Edwards’s Botanical Register, Vol. 15 (ed. Lindley, J. ), Cymaria, sub. t. 1292. (James Ridgway, London, 1830).

  99. 99

    Keng, H. Flora Malesianae precursores XLVIII: a revision of Malesian Labiatae. Gard. Bull. Sing. 24, 13–180 (1969).

    Google Scholar 

  100. 100

    Scheen, A. C. & Albert, V. A. Molecular phylogenetics of the Leucas group (Lamioideae; Lamiaceae). Syst. Bot. 34, 173–181 (2009).

    Article  Google Scholar 

  101. 101

    Mathiesen, C., Scheen, A. C. & Lindqvist, C. Phylogeny and biogeography of the lamioid genus Phlomis (Lamiaceae). Kew Bull. 66, 83–99 (2011).

    Article  Google Scholar 

  102. 102

    Bendiksby, M., Brysting, A. K., Thorbek, L., Gussarova, G. & Ryding, O. Molecular phylogeny and taxonomy of the genus Lamium L. (Lamiaceae): disentangling origins of presumed allotetraploids. Taxon 60, 986–1000 (2011).

    Article  Google Scholar 

  103. 103

    Scheen, A. C. & Albert, V. A. Nomenclatural and taxonomic changes within the Leucas clade (Lamioideae; Lamiaceae). Syst. Geogr. Plants 77, 229–238 (2007).

    Google Scholar 

  104. 104

    Bendiksby, M., Salmaki, Y., Bräuchler, C. & Ryding, O. The generic position of Stachys tibetica Vatke and amalgamation of the genera Eriophyton and Stachyopsis (Lamiaceae subfam. Lamioideae). Plant Syst. Evol. 300, 961–971 (2014).

    Article  Google Scholar 

  105. 105

    Cantino, P. D. & de Queiroz, K. International code of phylogenetic nomenclature, version 4c. (2010) Available at: https://www.ohio.edu/phylocode/. (Accessed: 20 December 2014).

  106. 106

    Cantino, P. D. et al. Towards a phylogenetic nomenclature of Tracheophyta. Taxon 56, 822–846 (2007).

    Article  Google Scholar 

  107. 107

    Cantino, P. D. & Abu-Asab, M. S. A new look at the enigmatic genus Wenchengia (Labiatae). Taxon 42, 339–344 (1993).

    Article  Google Scholar 

  108. 108

    Abu-Asab, M. S. & Cantino, P. D. Systematic implications of pollen morphology in subfamilies Lamioideae and Pogostemonoideae (Labiatae). Ann. Missouri Bot. Gard. 81, 653–686 (1994).

    Article  Google Scholar 

  109. 109

    Hsieh, T. H. & Huang, T. C. Notes on the flora of Taiwan (20)—Scutellaria (Lamiaceae) in Taiwan. Taiwania 40, 35–56 (1995).

    Google Scholar 

  110. 110

    Raj, B. A contribution to the pollen morphology of Verbenaceae. Rev. Palaeobot. Palynol. 39, 343–422 (1983).

    Article  Google Scholar 

  111. 111

    Ma, Z. H., Bramley, G. L. C. & Zhang, D. X. Pollen morphology of Callicarpa L. (Lamiaceae) from China and its systematic implication. Plant Syst. Evol. 302, 67–88 (2015).

    Article  Google Scholar 

  112. 112

    D’Arcy, W. G. Jacquin names, some notes on their typification. Taxon 19(4), 554–560 (1970).

    Article  Google Scholar 

  113. 113

    Wiens, J. J. Can incomplete taxa rescue phylogenetic analyses from long branch attraction? Syst. Biol. 54, 731–742 (2005).

    Article  PubMed  Google Scholar 

  114. 114

    Wiens, J. J. & Moen, D. Missing data and the accuracy of Bayesian phylogenetics. J. Syst. Evol. 46, 307–314 (2008).

    Google Scholar 

  115. 115

    Doyle, J. J. & Doyle, J. D. A rapid DNA isolation procedure for small quantities of fresh leaf tissue. Phytochem. Bull. 19, 11–15 (1987).

    Google Scholar 

  116. 116

    Gene Codes Corporation. Sequencher, version 4.5. (2005) Available at: http://genecodes.com/. (Accessed: 13 March 2011).

  117. 117

    Larkin, M. A. et al. Clustal W and Clustal X version 2.0. Bioinformatics 23, 2947–2948 (2007).

    Article  CAS  Google Scholar 

  118. 118

    Hall, T. A. BioEdit: A user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucl. Acids Symp. Ser. 41, 95–98 (1999).

    CAS  Google Scholar 

  119. 119

    Young, N. D. & Healy, J. GapCoder automates the use of indel characters in phylogenetic analysis. BMC Bioinformatics 4, 6 (2003).

    Article  PubMed  PubMed Central  Google Scholar 

  120. 120

    Swofford, D. L. PAUP*: Phylogenetic analysis using parsimony (*and other methods), version 4.0b10. (Sinauer, Massachusetts, Sunderland, 2002).

  121. 121

    Stamatakis, A., Hoover, P. & Rougemont, J. A rapid bootstrap algorithm for the RAxML web-servers. Syst. Biol. 75, 758–771 (2008).

    Article  Google Scholar 

  122. 122

    Ronquist, F. et al. MrBayes 3.2: efficient Bayesian phylogenetic inference and model choice across a large model space. Syst. Biol. 61, 539–542 (2012).

    Article  PubMed  PubMed Central  Google Scholar 

  123. 123

    Miller, M. A., Pfeiffer, W. & Schwartz, T. Creating the CIPRES Science Gateway for inference of large phylogenetic trees in Proceedings of the Gateway Computing Environments Workshop (GCE), USA 1–8 (New Orleans, LA., 2010).

  124. 124

    Posada, D. & Crandall, K. A. Modeltest: testing the model of DNA substitution. Bioinformatics 14, 817–818 (1998).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  125. 125

    Rambaut, A., Suchard, M. A., Xie, D. & Drummond, A. J. Tracer v.1.6. (2014) Available at: http://beast.bio.ed.ac.uk/Tracer. (Accessed: 10 October 2015).

Download references


This work was supported by Ministry of Science and Technology of China (grant no. 2013FY111200), National Natural Science Foundation of China (grant no. 31460044), and National Science Foundation of the United States (DEB 1020369). Assistance in the lab was provided by P.A. Reeves and Y.W. Yuan.

Author information




Conceived and designed the experiments: B.L., D.-X.Z., P.D.C. and R.G.O. Collected the materials: B.L., C.-L.X., G.L.C.B., Y.-H.T. and Z.-H.M. Performed the experiments: B.L., C.-L.X., R.G.O. and Z.-H.M. Analyzed the data: B.L. and R.G.O. Wrote the paper: B.L., C.-L.X., D.-X.Z, G.L.C.B., P.D.C. and R.G.O.

Corresponding author

Correspondence to Dian-Xiang Zhang.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Supplementary information

Rights and permissions

This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Li, B., Cantino, P., Olmstead, R. et al. A large-scale chloroplast phylogeny of the Lamiaceae sheds new light on its subfamilial classification. Sci Rep 6, 34343 (2016). https://doi.org/10.1038/srep34343

Download citation

Further reading


By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.