We propose modifications to the Code such that use of a hyphen in the name of a fossil-genus is treated as an error to be corrected by deletion of the hyphen. This will circumvent the need to conserve the numerous de-hyphenated names against unused hyphenated forms. We propose changes to Art. 60 of the Code to allow this correction, and the addition of a phrase in Art. 20 to add clarity to the naming of fossil-genera.

Athroismeae is a small tribe of the Asteraceae-Asteroideae, the members of which show considerable variation in morphology. A molecular phylogenetic study of the tribe is presented for the first time, based on plastid (ndhF, trnH-psbA, trnL-trnF) and nuclear data (ETS, ITS). The phylogenetic relationships between the different genera within Athroismeae are discussed, and in addition, three unispecific genera: Anisochaeta, Artemisiopsis and Symphyllocarpus as well as Duhaldea (Inula) stuhlmannii, all earlier placed in other tribes, are here shown to belong within Athroismeae. Symphyllocarpus is sister to Centipeda and the earlier Symphyllocarpinae includes Centipedinae in synonymy. Furthermore, Cardosoa and Philyrophyllum are found to be integrated within Anisopappus and their generic status cannot be maintained. An outline of an amended circumscription of the Athroismeae is presented, with three new combinations and a description of the new subtribe Lowryanthinae.

Anisopappus (Asteraceae: Athroismeae) is a genus with its main distribution in Africa (one species also in Asia), currently considered to include around 21 species. A molecular phylogenetic study of Anisopappus is presented for the first time, based on plastid (ndhF, trnL-trnF, trnQ-rps16) and nuclear (ETS, ITS) data. Anisopappus is confirmed to be monophyletic, and species interrelationships are resolved. The results differ from earlier treatments based on morphology, and the phylogenetic analyses reveal a need for changes in species circumscriptions as compared to those of the most recent treatment. Consequently, many taxa currently treated as synonyms are here shown to represent separate species indicating that the genus includes well over 40 species. Distribution patterns now emerge where several clades are found to consist of species restricted to a particular geographical region. The Anisopappus of Madagascar, many of which were earlier placed in synonymy with species found on the African continent, are here shown to be endemic, and the results reveal a need for further studies of that group.

Phylogenetic relationships of the two Malagasy Sapotaceae endemic genera Capurodendron and Tsebona have been unclear until now. Recent collections from Madagascar, as well as a better representation of the tribe Isonandreae, altogether 95 terminals, were used to estimate a phylogeny of subfamily Sapotoideae. We analysed sequences of nrDNA (ITS) and cpDNA (trnH-psbA) with Bayesian inference and parsimony jackknifing. As in previous analyses, Sapoteae and Sideroxyleae are recovered monophyletic. In addition, Isonandreae, distributed in the Indo-Pacific, is for the first time resolved as monophy- letic and sister to Sapoteae. All Malagasy accessions of Capurodendron, Tsebona, and a new species are grouped in another well-supported clade. This clade is accommodated in a new tribe Tseboneae characterized by caducous stipules, 5-merous flowers with quincuncial sepals, contorted aestivation of corolla lobes, absence of corolla appendages, one or three stamens opposite each corolla lobe, villous staminodes, seeds with an adaxial scar and plano-convex cotyledons, lacking endosperm. The new species is described in the new genus Bemangidia (B. lowryi) because it has a unique leaf venation for the tribe and combines different morphological features from Capurodendron and Tsebona. All three genera are well-supported monophy- letic groups. Bemangidia lowryi is threatened with extinction due to extensive ongoing forest destruction and is assigned a preliminary conservation status of Critically Endangered.

The Inula complex (Asteraceae: Inulinae) is a monophyletic group which comprises eight genera distributed in Eurasia and Africa: Amblyocarpum, Carpesium, Chrysophthalmum, Inula, Pentanema, Rhanteriopsis, Telekia, and Varthemia. With the aim to shed light on the circumscription of these genera, phylogenetic analyses were performed with 293 new DNA sequences (ITS region from nrDNA and three plastid spacers from cpDNA: rps16-trnQ, rpl32-trnL, ndhF-rpl32). It is concluded that both Inula and Pentanema are paraphyletic and that generic delimitations within the Inula complex need to be revised. Based on the results of the analyses, together with morphological and karyological data, we argue that the best solution is a new circumscription of the genus Pentanema including an amended description and 24 new combinations of former Inula species. Resurrection of the names Codonocephalum, Monactinocephalus and Vicoa is proposed to preserve the monophyly of the genera included in the Inula complex. Incongruences between nrDNA and cpDNA are documented and discussed.

Phylogenetic relationships in the tribe Inuleae (Asteraceae, sunflower family) are elucidated based on a concatenated set of nuclear (ETS, ITS), and chloroplast data (ndhF, trnL-F, trnH-psbA), analysed by Bayesian and parsimony methods. Extensive sampling of representatives from both subtribes Inuleae-Inulinae and Inuleae-Plucheinae establish their reciprocal monophyly, and result in the first-ever resolved molecular phylogeny of the Inuleae-Plucheinae with new insights into the relationships and morphological character distributions between genera and among species. Of the 31 accepted genera in the Inuleae-Plucheinae, only Pseudoblepharispermum is not represented in this study, 12 monotypic genera are placed in the phylogeny, 13 genera are shown to be monophyletic, and only 5 of the remaining 18 genera are revealed to be polyphyletic. The implications for the nomenclature status of the monotypic and polyphyletic genera are discussed, together with a descriptive review of morphological characters traditionally used to circumscribe the genera in this subtribe.

Tropical Asia is one of the centers of species diversity of flowering plants, in particular the coffee family (Rubiaceae). Prismatomerideae (the Psychotrieae alliance, subfamily Rubioideae) are a mostly Southeast Asian tribe encompassing four genera of shrubs and small trees (monospecific Gentingia and Motleyia, Prismatomeris with 16 spp., Rennellia with 4–5 spp.). We conducted molecular phylogenetic analyses of this group based on the nuclear and plastid sequence data from six markers and using Bayesian inference. The main goal was to produce a robust phylogeny of the tribe, which was subsequently used to (1) reassess its monophyly and phylogenetic position within the Psychotrieae alliance; (2) rigorously test the monophyly of Prismatomeris and Rennellia; (3) assess the phylogenetic relationships between the genera; and (4) evaluate the phylogenetic value of the inflorescence type currently used for species recognition in Rennellia. Motleyia was not sequenced due to the lack of material, and therefore its affinity with the other genera was assessed based on morphology. The tribe was supported as monophyletic and resolved as sister to the (Gaertnereae (Mitchelleae-Morindeae)) clade. The monophyly of Prismatomeris sensu Johansson was strongly supported, but we argue for the merging of the monospecific genus Motleyia into Prismatomeris based on their strong morphological similarities coupled with the paraphyly of Prismatomeris with respect to Motleyia. Rennellia was strongly supported as paraphyletic with respect to Gentingia. We propose the transfer of the monospecific genus Gentingia to Rennellia, also consistent with their strong morphological resemblance. Prismatomerideae were resolved in two major sister lineages, the Prismatomeris and Rennellia clades, corresponding to our broadly delimited Prismatomeris and Rennellia. Three well-supported and morphologically distinct subclades were identified within Rennellia s.l., of which one was represented by Rennellia subsessilis, with sessile and reduced umbel-like inflorescences bearing two to four flowers. The other two subclades have compound spike-like (or sub-raceme-like) and raceme-like inflorescences, an important distinction in species-group recognition. We conclude that inflorescence type shows a strong phylogenetic signal and is, therefore, a reliable feature for recognizing groups of species in Rennellia. Additional taxonomic characters are, however, needed for teasing apart closely related species with the same inflorescence types. Subsequent to our taxonomic revision, the tribe Prismatomerideae comprises two genera: Prismatomeris and Rennellia. One and two new combinations, respectively, are presented, bringing the total number of species in the tribe to 25, of which 17 are in Prismatomeris and 8 in Rennellia. A new species key to Rennellia s.l. is presented.

Araucarioxylon Kraus is a widely known fossil-genus generally applied to woods similar to that of the extant Araucariaceae. However, since 1905, several researchers have pointed out that this name is an illegitimate junior nomenclatural synonym. At least four generic names are in current use for fossil wood of this type: Agathoxylon Hartig, Araucarioxylon, Dadoxylon Endl. and Dammaroxylon J.Schultze-Motel. This problem of inconsistent nomenclatural application is compounded by the fact that woods of this type represent a wide range of plants including basal pteridosperms, cordaitaleans, glossopterids, primitive conifers, and araucarian conifers, with a fossil record that extends from the Devonian to Holocene. Conservation of Araucarioxylon has been repeatedly suggested but never officially proposed. Since general use is a strong argument for conservation, a poll was conducted amongst fossil wood anatomists in order to canvass current and preferred usage. It was found that the community is divided, with about one-fifth recommending retention of the well-known Araucarioxylon, whereas the majority of others advocated use of the legitimate Agathoxylon. The arguments of the various colleagues who answered the poll are synthesized and discussed. There is clearly little support for conservation of Araucarioxylon. A secondary aspect of the poll tackled the issue as to whether Araucaria-like fossil woods should be either gathered into a unique fossil-genus, or whether two fossil-genera should be recognized, based on the respective presence or absence of axial parenchyma. A majority of colleagues favoured having one fossil-genus only. Agathoxylon can be used legitimately and appears to be the most appropriate name for such woods. However, its original diagnosis must be expanded if those woods lacking axial parenchyma are to be included.

Classifications of the pantropical plant family Sapotaceae based solely on morphology have historically recognized be- tween 125 and 53 genera. Phylogenetic analyses using molecular data have repeatedly demonstrated that broad concepts of two large genera belonging to subfamily Chrysophylloideae, Chrysophyllum and Pouteria, are untenable and their narrowed delimitations have restricted them to the Neotropics. A recent phylogenetic study proposed further amendments by resurrecting the genera Achrouteria, Cornuella, Lucuma, Martiusella, Nemaluma, Prieurella and Ragala, and questioned the status of three generally accepted genera, Chromolucuma, Pradosia and Sarcaulus. We test this suggested classification using expanded sampling that comprises 122 terminals, including material of 29 of the 34 name-bringing species for generic names historically regarded as synonyms of Chrysophyllum and Pouteria. We used sequence data from ribosomal nrDNA (ETS, ITS), the nuclear gene RPB2, two cpDNA spacers (petN-psbM, trnH- psbA), and indel information to estimate phylogenetic relationships in a Bayesian framework using BEAST. All sequences were newly realigned to test reproducibility, and 26 morphological characters were mapped on the resulting tree. Our analyses recovered three African genera embedded within a large Neotropical clade of Chrysophylloideae. We found strong support for the reinstatement of the seven genera listed above as well as for four other genera, viz. Chloroluma, Englerella, Labatia, and Peteniodendron. This sub- sequently leads to further amendments of Chrysophyllum and Pouteria, which are now limited to include 25–30 and 7 species, respec- tively. However, one clade that includes many name-bringing lineages largely corresponds to Pouteria s.l., a group that needs further phylogenetic research to unravel relationships and generic limits. The hypothesis that Chrysophyllum cuneifolium had an inter- continental hybrid origin involving genomes from Africa and South America is rejected because it is shown to have been based on erroneous results obtained from a contaminated DNA aliquot. A total of 73 genera are currently recognised in Sapotaceae, 21 of which are Neotropical members of Chrysophylloideae. We update the nomenclature and synonymy of 75 species, make 36 new com- binations, and designate lectotypes for 31 names.

ThepantropicalplantfamilySapotaceaecurrentlyincludes65–70genera.Twogenera,BeauvisageaandBoerlagella,were described in 1890s using incomplete material from West New Guinea (Bird’s Head Peninsula) and Sumatra, neither of which has been collected since. Their systematic position has long been regarded doubtful and Boerlagella was once placed in its own family, Boer- lagellaceae. We show here how useful and important it can be to obtain small leaf fragments from type specimens that are up to 150 years old for molecular analysis aiming to determine their phylogenetic position and clarify their taxonomic status. We used nuclear ribosomal DNA (ETS, ITS) and the nuclear gene RPB2 from 170 terminals to estimate phylogenetic relationships in a Bayes- ian framework using BEAST. The old type material yielded full length sequences of ETS and ITS from both genera (less successful with RPB2), revealing that both are firmly placed in Planchonella. Boerlagella is placed in synonymy with Planchonella and its type is accepted as Planchonella spectabilis, a species from Sumatra that possibly has gone extinct due to deforestation. Beauvisagea from the Bird’s Head Peninsula of western New Guinea is likewise regarded as a synonym of Planchonella and its type, accepted as P. pomi- fera, is conspecific with Pouteria doonsaf (currently circumscribed to include material of at least two different species), not Plancho- nella maclayana as earlier believed. Our study also included Planchonella suboppositifolia, an odd species with a character combination in conflict with the current definition of the genus. Our results show that it is sister to a lineage comprising several gen- era, including Planchonella, and that it represents a distinct lineage constituting a monotypic genus that will be described in a sub- sequent paper. The most recent classification of subfamily Chrysophylloideae and the character combinations used to distinguish its constituent genera are supported, and our results confirm that taxa can reliably be assigned to a genus based on morphology alone. 

PouteriasplendensistheonlynativespeciesofSapotaceaeinChile,aspeciesonceplacedinthemonotypicgenusGayella and known as G. valparadisaea, but for a long time treated as a Pouteria. In a phylogenetic analysis, this species was placed in an Australasian clade, not with its presumed relatives in South America. We used Bayesian inference under a relaxed molecular clock in BEAST, nuclear ribosomal DNA (ETS, ITS), the nuclear gene RPB2, indel information, and 201 terminals to find the closest rel- ative of P. splendens and to estimate the age of the disjunction between Australasia and South America. The taxon has an isolated phylogenetic position, being part of the cladeʼs backbone, and is placed with weak support as sister to Van-royena, another monotypic genus, but endemic to Australia. Our results justify reinstatement of Gayella with its single species G. valparadisaea. Gayella has a unique combination of morphological features including alternate, opposite or 3-whorled leaves, often on the same plant, a usually 6-lobed, rotate corolla with revolute corolla lobes giving the flower a star-like appearance, lacerate to dentate staminodes, and yellow-orange-red fruit with plano-convex cotyledons and an exserted radicle below the cotyledon commissure. The split between Gayella and Van-royena is estimated to the late Eocene at about 40.0 Ma (50.5–25.3 Ma). The hypothesis that the presence of Gayella in South America is a result of vicariance is consistent with the timing of the geological splits of southern Gondwana, as well as with evidence from fossil pollen, but long-distance dispersal is an alternative explanation that cannot be excluded. Gayella is restricted to an area with a Mediterranean-type climate in coastal central Chile, where it occurs in rocky places, ravines, and gullies, usually below 100 m altitude within reach of sea mist. Gayella valparadisaea is a rare plant, listed as Endangered (EN) in Chile, but it does not occur in any protected area. Considering the isolated phylogenetic position of this old lineage, we urge the Chilean authorities to increase the efforts towards protection of this species.

Generic limits within subfamily Chrysophylloideae (Sapotaceae) from Oceania and Southeast Asia are reconciled based on a molecular phylogeny. We analysed sequences of nuclear ribosomal DNA (ETS, ITS) and the nuclear gene RPB2 with BEAST and parsimony jackknifing, using a sample of 168 terminals. Eight morphological characters were traced on a condensed majority-rule consensus tree to identify diagnostic character combinations for the genera. Accepted genera with character support are Magodendron, Pichonia, Planchonella, Pycnandra, Sersalisia, and Van-royena, while Beccariella and Niemeyera require amendment. Beccariella, a widely distributed group, is an illegitimate later homonym and we propose that the genus Pleioluma is resurrected in its place. The Australian genus Niemeyera is paraphyletic, but it is rendered monophyletic by reinstating Amorphospermum for N. antiloga. Beauvisagea, Blabeia, Fontbrunea, and Krausella are all segregates of Planchonella and rejected, while Wokoia is a later synonym of Pichonia. Planchonella baillonii, an endemic species of New Caledonia, is the sole member of an old lineage and firmly placed as the sister to a clade comprising the other congeners. Planchonella sandwicensis, a Hawaiian species, previously proposed to be a distinct genus, is a member of Planchonella. In the Pacific, P. tahitensis (including P. grayana) is a polymorphic species, widely distributed and adapted to a wide range of habitats. We provide a generic key (excluding Xantolis), diagnostic character combinations for all genera, and the necessary taxonomic combinations for Pichonia, Planchonella, Pleioluma, and Sersalisia to render each genus monophyletic.