Molecular phylogeny of the beetle tribe Oxypodini (Coleoptera: Staphylinidae: Aleocharinae)

This is the first study to comprehensively address the phylogeny of the tribe Oxypodini Thomson and its phylogenetic relationships to other tribes within the staphylinid subfamily Aleocharinae. Using the hitherto largest molecular dataset of Aleocharinae comprising of 4599 bp for representatives of 22 tribes, the Oxypodini are recovered as non‐monophyletic. Members of the tribe belong to three distantly related lineages within the Aleocharinae: (i) the Amarochara group as sister clade to the tribe Aleocharini, (ii) the subtribe Tachyusina within a clade that also includes the tribes Athetini and Hygronomini, (iii) all other Oxypodini in a clade that also includes the tribes Placusini, Hoplandriini and Liparocephalini. Based on the inferred phylogeny, five subtribes of the Oxypodini are recognized: Dinardina Mulsant & Rey, Meoticina Seevers, Microglottina Fenyes, Oxypodina Thomson and Phloeoporina Thomson. The following changes in the classification of the Aleocharinae are proposed: (i) Amarochara Thomson is removed from the Oxypodini and placed in the tribe Aleocharini; (ii) the subtribe Taxicerina Lohse of the Athetini is reinstated as tribe Taxicerini to include Discerota Mulsant & Rey, Halobrecta Thomson (both removed from the Oxypodini) and Taxicera Mulsant & Rey; (iii) the subtribe Tachyusina Thomson is excluded from the Oxypodini and provisionally treated as tribe Tachyusini; (iv) the oxypodine subtribe name Blepharhymenina Klimaszewski & Peck is placed in synonymy with the subtribe name Dinardina Mulsant & Rey.     

Palynological Features as a Systematic Marker in Artemisia L. and Related Genera (Asteraceae, Anthemideae) - II: Implications for Subtribe Artemisiinae Delimitation

Abstract: Using optical and scanning electron microscopy, we completed a palynological study of the subtribe Artemisiinae (Asteraceae, Anthemideae), which we started in a previous paper. This subtribe contains different genera with a systematic position that, in many cases, has been controversial. There is a group of genera closely related to Artemisia, and another one more related to Chrysanthemum sensu lato. We confirm the existence of two pollen morphological patterns - concerning exine ornamentation - in the tribe Anthemideae and in the subtribe Artemisiinae as currently considered: one with long spines ( Anthemis type) and the other with short spinules ( Artemisia type). This feature is a good taxonomic marker, well correlated with other morphological and with molecular characters. This enables a new delimitation of the subtribe Artemisiinae, which is characterized by pollen grain ornamentation constituted by short spinules (microechinate pollen), and should be restricted to Artemisia and the closely related genera that share this trait.     

Pericarp structure and systematic positions of five genera of Lamiaceae subg. Nepetoideae tribe Ocimeae

Pericarp structure has been investigated in five genera of Lamiaceae subg. Nepetoideae tribe Ocimeae which were omitted or poorly studied by Ryding (1992a): Hanceola, Limniboza, Skapanthus, Tetradenia and Thorncroftia . In the light of the results, the systematic position of these and some related genera are discussed. Limniboza is suggested to belong to Ocimeae subtribe Ociminae, the Acrocephalus group. Hanceola (incl. Siphocranion), Isodon, Skapanthus (which is resurrected as a genus), Tetradenia and Thorncroftia apparently do not fit into any of the three traditional subtribes (Hyptidinae, Ociminae or Plectranthinae). The three Asiatic genera, Hanceola, Isodon and Skapanthus might together form a new subtribe. Tetradenia and Thorncroftia have more isolated positions in the Ocimeae.     

Phylogenetic relationships of subtribe Ecliptinae (Asteraceae: Heliantheae) based on chloroplast DNA restriction site data

Phylogenetic analysis of chloroplast DNA restriction site data for 76 of the 302 genera of Heliantheae sensu lato using 16 restriction endonucleases reveals that subtribe Ecliptinae is polyphyletic and that its genera are distributed in four different lineages. The ecliptinous genera Squamopappus, Podachaenium, Verbesina, and Tetrachyron (of the Neurolaeninae), along with other members of subtribe Neurolaeninae are the basalmost clades of the paleaceous Heliantheae. The mostly temperate species of subtribe Ecliptinae (exemplified by Balsamorhiza, Borrichia, Chrysogonum, Engelmannia, Silphium, Vigethia, and Wyethia) are strongly nested in a clade with the Mesoamerican monotypic genus Rojasianthe as basal. The genera characterized by marcescent ray corollas traditionally classified in subtribe Zinniinae constitute a strongly supported group sister to Acmella, Spilanthes, and Salmea. The largest clade of ecliptinous genera is the most recently derived group within Heliantheae sampled. This large group of mostly Neotropical lowland genera (variously characterized by their winged cypselae, foliaceous phyllaries, and opposite phyllotaxy and exemplified by Perymenium, Wedelia, and Zexmenia) has been and continues to be the most challenging group from a taxonomic standpoint. The study provides new insights as to their relationships that will have a positive impact in future monographic studies of the group. The genera of the Espeletiinae form a monophyletic clade and are sister to members of the Milleriinae and Melampodiinae. This result is consistent with their traditional taxonomic placement with genera such as Smallanthus with which they share a tendency for functionally staminate disc flowers. The phylogenetically enigmatic genus Montanoa is sister to Melampodium. Members of subtribe Galinsoginae are clustered in two main lineages that correspond to the traditional division of the subtribe based on pappus characteristics. There is no support for the monophyly of subtribe Galinsoginae, and the same results indicate some of its genera are paraphyletic.     

Phylogeny and molecular evolution of the tribe Harpalini (Coleoptera, Carabidae) inferred from mitochondrial cytochrome-oxidase I

The tribe Harpalini is a group of ground beetles with a world-wide distribution that comprises approximately 2000 species and about 238 genera and subgenera. Hypotheses about the phylogenetic relationships of the subtribes of Harpalini are implicit within the systematic criteria put forward by different authors. A 759 bp fragment of the mitochondrial COI was sequenced in 119 specimens (107 species) of 52 genera and subgenera that represent the main lineages of Harpalines, and 3 species of other tribes used as outgroups. A hierarchical study of sequence divergence (under uncorrected and corrected models) and ts:tv ratio pattern analyses were carried out at different taxonomic levels. A low saturation rate was detected at first and second codon positions, whereas A+T richness causes a low transitions:transversions ratio, which suggests--a priori--a high rate of saturation at the third codon position. A progressive accumulation of sequence divergence and a decreasing ts:tv ratio were found from lower to higher taxonomic levels. MP strict consensus, ML, and minimum evolution distance (under ts+tv and tv only schemes) trees showed similar major clades within the tribe. The subtribe Ditomina is a monophyletic lineage with close affinities to the subtribe Harpalina. Harpalina is a polyphyletic lineage as the genus Daptus is always related to members of the subtribe Stenolophina, and the Selenophorines resulted a polyphyletic group related to the subtribe Anisodactylina. Main lineages proposed by Noonan [Quaest. Entomol. 9 (1973) 266] within the subtribe Anisodactylina have been corroborated in this study. The Australian genus Phorticosomus is not related to Ditomina but to the Australian Notiobioids lineage. Most taxa of the subtribe Stenolophina are always included in the same clade, together with taxa of the subtribe Pelmatellina, which might be considered as a lineage of Stenolophina related to Bradycellus and Dicheirotrichus. The subtribe Amblystomina lacks a well-supported relationship to the other subtribes of Harpalini and could not be consistently related to any of them.     

Phylogeny of the riodinid butterfly subtribe Theopeina (Lepidoptera: Riodinidae: Nymphidiini)

Abstract The almost exclusively Neotropical butterfly family Riodinidae is poorly represented in both ecological and systematic studies of Lepidoptera. A comparative morphological study of all seventy-five species in subtribe Theopeina (tribe Nymphidiini) yielded 104 characters, predominantly from wing pattern, male and female genitalia, and abdominal structures. All morphological characters and adults representing the range of wing pattern variation are illustrated. Phylogenetic analysis of the data produced a large number of most parsimonious cladograms, but the strict consensus of these, both when using equal weights and after successive weighting, is well resolved and the majority of terminal clades have high character and branch support. Theopeina is found to consist of five monophyletic genera, Protonymphidia , Archaeonympha , Calicosama , Behemothia and Theope (=  Parnes and Dinoplotis ), with the largest genus Theope containing thirteen monophyletic species groups, which are delineated to facilitate a discussion of broad evolutionary patterns in this morphologically diverse subtribe.     

The Genus Artemisia and its Allies: Phylogeny of the Subtribe Artemisiinae (Asteraceae, Anthemideae) Based on Nucleotide Sequences of Nuclear Ribosomal DNA Internal Transcribed Spacers (ITS)

Abstract: Sequences of the internal transcribed spacers (ITS1 and ITS2) of nuclear ribosomal DNA were analysed for 44 Artemisia species (46 populations) representing all the five classical subgenera and the geographical range of the genus, 11 species from 10 genera closely related to Artemisia, and six outgroup species from five other genera of the Anthemideae. The results definitely support the monophyly of the genus Artemisia in its broadest sense (including some taxa segregated as independent genera, like Oligosporus and Seriphidium ). Eight main clades are established in this molecular phylogeny within Artemisia; they agree in part with the classical subdivision of the genus, but they also suggest that some infrageneric groups must be redefined, especially the subgenus Artemisia. The subgenera Tridentatae and Seriphidium are independent from each other. Some of the satellite genera are clearly placed within Artemisia ( Artemisiastrum, Filifolium, Mausolea, Picrothamnus, Sphaeromeria, Turaniphytum ), whereas some others fall outside the large clade formed by this genus (Brachanthemum, Elachanthemum, Hippolytia, Kaschgaria). Our results, correlated to other data such as pollen morphology, allow us to conclude that the subtribe Artemisiinae as currently defined is a very heterogeneous group. Affinities of the largest genus of the subtribe and tribe, Artemisia, and of other genera of the subtribe to some genera from other subtribes of the Anthemideae strongly suggest that subtribe Artemisiinae needs a deep revision and redefinition. Phylogenetic utility of region trnL-F of the plastid DNA in the genus Artemisia and allies was also evaluated: sequences of the trnL-F region in Artemisia do not provide phylogenetic information.     

A phylogenetic analysis of the palm subtribe Oncospermatinae (Arecaceae) based on morphological characters

Subtribe Oncospermatinae (Arecaceae: Arecoideae: Areceae) is a diverse group of spiny Old World palms. The subtribe includesOncosperma, a widespread Asian genus of five species, along with seven monotypic genera, all endemic to the Seychelles and Mascarene Islands of the western Indian Ocean. A phylogenetic analysis was conducted in order to test the monophyly of subtribe Oncospermatinae with respect to other Old World genera of tribe Areceae. A matrix of 38 morphological characters was scored for 29 taxa, including 11 species of the Oncospermatinae. A single most parsimonious tree was found, resolving the subtribe as a polyphyletic group of two distinct clades. One clade containingAcanthophoenix, Deckenia, Oncosperma, andTectiphiala was placed as sister to a large group that includes members of subtribes Archontophoenicinae, Arecinae, Iguanurinae, and Ptychospermatinae. The other clade of Oncospermatinae, including the Seychelles endemic generaNephrosperma, Phoenicophorium, Roscheria, andVerschaffeltia, was resolved as sister to the Madagascar endemic subtribe Masoalinae, and may have arisen in the western Indian Ocean region.     

An ITS phylogeny of Balsamorhiza and Wyethia (Asteraceae: Heliantheae)

The relationships among the species of Balsamorhiza and Wyethia (Asteraceae: Heliantheae) were examined using data from the internal transcribed spacer (ITS) region of the nuclear ribosomal DNA. The ITS sequences were obtained from nine species of Balsamorhiza and 14 species of Wyethia as well as seven outgroup genera. Five of the outgroup genera were members of the subtribe Engelmanniinae of the tribe Heliantheae, the subtribe that includes Balsamorhiza and Wyethia. The resulting trees show that Balsamorhiza and Wyethia together form a monophyletic group. Balsamorhiza alone is monophyletic, but neither of its two sections is monophyletic. Wyethia is paraphyletic. One group of Wyethia species, including all members of sections Alarconia and Wyethia as well as W. bolanderi from section Agnorhiza, is monophyletic and sister to Balsamorhiza. The other species of Wyethia (all placed in section Agnorhiza) are part of a polytomy along with the clade composed of Balsamorhiza plus the rest of Wyethia.     

Polyphyly of the grass tribe Hainardieae (Poaceae: Pooideae): identification of its different lineages based on molecular phylogenetics, including morphological and cytogenetic characteristics

The small pooid grass tribe Hainardieae comprises six genera with approximately ten species; however, this tribe was not accepted by all previous taxonomic treatments. To study the relationships among these genera and to infer the phylogeny and evolutionary patterns, we used sequence variation of the internal transcribed spacers (ITS) of nuclear ribosomal and chloroplast (cp) matK DNA and morphology. Many genera of the Aveneae/Poeae tribe complex additionally were included. Both molecular datasets showed Hainardieae to be highly polyphyletic, and its genera to branch with different groups of the Aveneae/Poeae. Parapholis and Hainardia are corroborated as being closely related, and belonging to a firmly supported Eurasian clade together with Catapodium incl. Scleropoa, Cutandia, Desmazeria, Sphenopus, Vulpiella (subtribe Parapholiinae) and with Cynosurus as sister to this assemblage. The other genera of traditionally recognised Hainardieae are positioned phylogenetically distant: Mediterranean Narduroides is verified as more or less related to Festuca and relatives (subtribe Loliinae), whereas the west Eurasian Pholiurus is close to the lineage of Poa and relatives (subtribe Poinae). North American Scribneria is sister to Deschampsia and both genera should be unified under a common subtribe (Aristaveninae or Holcinae). The phylogenetic position of the Algerian genus Agropyropsis (close to Narduroides and within the Loliinae) is suggested on morphology only, because no molecular data was obtained for it. Considering classification, we support the abandonment of tribe Hainardieae and argue to abandon Poeae subtribe Scribneriinae. Poeae subtribe Parapholiinae is redefined with a novel genus content, due to the exclusion of Agropyropsis and Pholiurus and the inclusion of Vulpiella.     

Revised concept of the genus Euryporus Erichson (Coleoptera, Staphylinidae, Staphylininae) and phylogenetic significance of Staphylinini from New Guinea

The Staphylinini rove beetle genus Euryporus Erichson from the subtribe Quediina is restricted to include only three species from the Western Palearctic region: Euryporus picipes (Paykull, 1800), Euryporus aeneiventris (Lucas, 1846), and Euryporus princeps Wollaston, 1864. Euryporus argentatus Fauvel, 1881, Euryporus warisensis Last, 1987 and Euryporus multicavus Last, 1980, which do not even belong to the subtribe Quediina, are excluded fromthe genus. Of these, two were transferred to different genera: Tympanophorus argentatus (Fauvel, 1881), comb. nov., from Sumatra;and Hesperus warisensis (Last, 1987), comb. nov.,from New Guinea. "Euryporus" multicavus could not be placed to any of the described genera of Staphylinini and is left as incertae sedis pending a broader study of the relevant fauna of this tribe in New Guinea and adjacent regions. The taxonomic history of Euryporus is reviewed, and an updated diagnosis of this genus is provided.     

Systematic implications of sesquiterpene lactones in the subtribe melampodiinae

Within the tribe Heliantheae of the Asteraceae, the genetic boundaries of the subtribe Melampodinae have recently been drastically revised by Stuessy. The number of genera within the subtribe has been reduced and new generic groupings have been established. The present study correlates the distribution of sesquiterpene lactones found in these genera with the newly revised subtribal boundaries. The genera Acanthospermum, Melampodium, Polymnia and Sigesbeckia produce predominantly melampolide-type sequiterpene lactones. Limited chemical data support Stuessy's removal of the genera Desmanthodium, Clibadium and Ichthyothere from the subtribe Melampodiinae. The occurrence of melampolide-type sesquiterpene lactones in members of the genera Tetragonotheca (Helianthinae) and Enhydra (Ecliptinae) indicate a possible position of these genera in the Melampodiinae.     

Phylogenetic position of the genus Ferula (Apiaceae) and its placement in tribe Scandiceae as inferred from nrDNA ITS sequence variation

Recent molecular systematic investigations suggested that Ferula, an umbellifer genus of about 170 species, is polyphyletic, with its members placed in the apioid superclade and within tribe Scandiceae. We analyzed ITS sequence variation from 134 accessions of Apiaceae, including 83 accessions (74 species) of Ferula to ascertain the phylogenetic position of the genus within the family. Phylogenetic analyses of these data using maximum parsimony, Bayesian, and neighbor-joining methods support the monophyly of Ferula upon the addition of Dorema and Leutea (as Ferula sensu lato) and its placement in tribe Scandiceae. Ferula sensu is closely allied with other major lineages of Scandiceae, corresponding to subtribes Scandicinae, Daucinae, and Torilidinae. Therefore, we recognize the Ferula clade as subtribe Ferulinae. Another addition to tribe Scandiceae is a clade composed of genera Glaucosciadium and Mozaffariania. The three accessions of Ferula misplaced in the apioid superclade represent a species of Silaum.     

A Phylogenetic Study of Tribe Euphorbieae (Euphorbiaceae)

A phylogenetic investigation of a monophyletic lineage of spurge plants, tribe Euphorbieae, was conducted to elucidate evolutionary relationships, to clarify biogeographic patterns, and to reexamine the previous classification of Euphorbieae. Cladistic analyses of the 52 morphological characters of 61 species resulted in 2922 equally most parsimonious trees of 193 steps with a consistency index of 0.34. The strict consensus tree indicates genus Anthostema of subtribe Anthosteminae as a likely sister group to all other members of tribe Euphorbieae. The morphological data support a monophyletic origin of subtribe Euphorbiinae, but the subtribes Anthosteminae and Neoquillauminiinae did not form monophyletic groups. Although the previous taxonomic treatments within tribe Euphorbieae have supported the generic status of Pedilanthus, Monadenium, Synadenium, Chamaesyce, and Elaeophorbia, the results of this analysis do not support generic placement of them based on cladistic principles. Recognition of these groups as genera results in Euphorbia becoming a paraphyletic group. One solution to this problem in Euphorbieae is to divide the largest genus Euphorbia into several monophyletic genera and to keep the generic ranks for previously recognized genera. The distribution of basal endemic genera in Euphorbieae showed African and east Gondwanan affinities and strongly indicated that the ancestor of Euphorbieae originated prior to the breakup of Gondwanaland from an old group in Euphorbiaceae. However, some recent African taxa of Euphorbia should be interpreted by transoceanic dispersal from the New World ancestors.     

<Emphasis Type="Italic">Welwitschiella</Emphasis> is a member of the African subtribe Grangeinae (Asteraceae Astereae): a new phylogenetic position based on <Emphasis Type="Italic">ndh</Emphasis>F and ITS sequence data

The African genus Welwitschiella has traditionally been placed in tribe Heliantheae. Our phylogenetic analysis of chloroplast DNA ndhF sequence data, however, reveals that it is part of tribe Astereae. In order to assess the relationships of this genus within the tribe, we produced a phylogeny based on ITS (nrDNA) sequence data of a sample including Amellus, African Conyza, Chrysocoma, Felicia spp., Mairia, Poeciliopsis, Printzia, Welwitschiella and Zyrphelis. Both parsimony and Bayesian analyses were done. The Bayesian analysis showed that African genera form a basal grade in tribe Astereae along with the Chinese Nannoglottis and South American and New Zealand genera, with Printzia being the earliest diverging member of the tribe. Mairia occupies an isolated position. Amellus, Chrysocoma, Felicia, Poecilolepis and Zyrphelis belong to subtribe Homochrominae, a South African radiation that also includes the St Helena endemics Commidendron and Melanodendron. Pteronia appears isolated, though it might be close to the Homochrominae. Welwitschiella is placed in the latest diverging African clade, subtribe Grangeinae, which also includes Grangea, Psiadia, Nidorella, and the African Conyza species except C. gouani. This subtribe is sister to the Eurasiatic subtribe Bellidinae, and together they are sister to the Astereae crown lineages of Australasia-Asia and South and North America.     

A Revision of Subtribe Pleioblastinae Keng & Keng f.

This paper deals with the taxa of tribe Arundinarieae Steud. subtribe Pleiobalastinae Keng and Keng f. which comprised three genera (Pseudosasa Makino, Pleioblastus Nakai and Brachystachyum Keng) when it was established in 1957. With the analysis of morphological characters and geographical distribution, a number of revisions connected with the taxon are made as follows: (1) Genus Brachystachyum Keng is transferred to the tribe Shibataeeae Nakai according to its false inflorescence. (2) Genus Pseudosasa Makino is transferred to subtribe Sasinae Keng f. according to our study on the numerical taxonomic method. (3) Some species of Pleioblastus Nakai established by Keng and Keng f. should be revised. Pleioblastus actinotrichus (Merr. and Chun) Keng f. should be Ampelocalamus actinotrichus (Merr. and Chun) S. L. Chen, T. H. Wen and G. Y. Sheng in subtribe Thamnocalaminae Keng f.; Pleioblastus dolichanthus (Keng) Keng f. is the synonym of Sinobambusa tootsik (Sieb.) Makino, belonging to tribe Shibataeeae Nakai. The rest species remain in this genus. Since the genus Pleioblastus is related to genus Arundinaria Michaux., subtribe Pleioblastus Keng and Keng f. does not seem to have a reason to be retained as a subtribe in tribe Arundinarieae Steud., according to the newest Code (1978). A part of it should be a synonym of subtribe Arundinariinae and we may cite it as follows: Subtribe Arundinariinae——Subtribe Pleioblastinae Keng and Keng f. pro parte, syn. nov. The other parts of it should be transferred to other subtribes or tribes. In addition, one new variety in Branchystachyum, two new species, one new variety in Pseudosasa and six new species, three new varieties in Pleioblastus, are described in this paper.     

Cymbonotus (Compositae: Arctotideae, Arctotidinae): an endemic Australian genus embedded in a southern African clade

The Compositae (Asteraceae) is the largest flowering plant family if described, accepted taxa are considered. Recent revisions in the taxonomy of the family have resulted in the recognition of ten subfamilies and 35 tribes. The tribe Arctotideae is one of the smallest, with around 200 species; it contains two subtribes and several hard-to-place taxa. Previous work has shown that the subtribe Arctotidinae is well defined and is restricted to southern Africa, except for the Australian genus Cymbonotus . Molecular data from internal transcribed spacer (ITS), ndh F, and trn L-F sequences were used (24 previously published sequences; 47 new sequences) to determine the patterns of relationships within the subtribe. Twenty-three samples from the ingroup, including members of all genera and all three species of Cymbonotus , were included in the analysis, together with two outgroup taxa. Cymbonotus is monophyletic and deeply embedded in the subtribe; Haplocarpha is paraphyletic and basal in position; all other genera are monophyletic; however, Arctotis has over 60 species and only eight were sampled for this study, so additional work may prove otherwise. Arctotis is nested high in the tree and has short branch lengths; this may reflect recent radiation. By contrast, the species of the paraphyletic and basal Haplocarpha have long branches, which may indicate an older radiation and a shared ancestry with the remainder of the subtribe. The presence of Cymbonotus in Australia is most probably the result of long-distance dispersal.  Journal compilation © 2007 The Linnean Society of London, Botanical Journal of the Linnean Society , 2007, 153 , 1–8. No claim to original US government works