Phylogeny of minute carabid beetles and their relatives based upon DNA sequence data (Coleoptera, Carabidae, Trechitae)

The phylogeny of ground beetles of supertribe Trechitae is inferred using DNA sequences of genes that code for 28S ribosomal RNA, 18S ribosomal RNA, and wingless. Within the outgroups, austral psydrines are inferred to be monophyletic, and separate from the three genera of true Psydrina (Psydrus, Nomius, Laccocenus); the austral psydrines are formally removed from Psydrini and are treated herein as their own tribe, Moriomorphini Sloane. All three genes place Gehringia with Psydrina. Trechitae is inferred to be monophyletic, and sister to Patrobini.Within trechites, evidence is presented that Tasmanitachoides is not a tachyine, but is instead a member of Trechini. Perileptus is a member of subtribe Trechodina. Against Erwin's hypothesis of anillines as a polyphyletic lineage derived from the tachyine genus Paratachys, the anillines sampled are monophyletic, and not related to Paratachys. Zolini, Pogonini, Tachyina, and Xystosomina are all monophyletic, with the latter two being sister groups. The relationships of the subtribe Bembidiina were studied in greater detail. Phrypeus is only distantly related to Bembidion, and there is no evidence from sequence data that it belongs within Bembidiina. Three groups that have been recently considered to be outside of the large genus Bembidion are shown to be derived members of Bembidion, related to subgroups: Cillenus is related to the Ocydromus complex of Bembidion, Zecillenus is related to the New Zealand subgenus Zeplataphus, and Hydrium is close to subgenus Metallina. The relationships among major lineages of Trechitae are not, however, resolved with these data.     

Chromosomal diversity and evolution in the ground beetle genus Bembidion and related taxa (Coleoptera: Carabidae: Trechitae)

Chromosome numbers and sex chromosome systems of 154 previously unstudied Bembidion species are described. The genus is nearly uniform: males of 176 of 205 species are 2n=22+XY. Karyotypes are presented for 30 species. There is some variation among species in size of Y and size of autosomes. Within most species autosomes are subequal in size, and metacentric or submetacentric. Subterminal secondary constrictions and B chromosomes are reported from several species.The supertribe Trechitae (Zolini + Trechini + Pogonini + Bembidiini) is hypothesized to be primitively male 2n=22+X or 24+X, and the ancestral Bembidion stock 2n=22+XY. Conclusions are based on the most parsimonious hypothesis of ancestral state given an inferred phylogeny of the group, rather than the widespread-is-primitive arguments used previously. Evolution within Bembidion away from the presumably-primitive 2n=22+XY is discussed. Six lineages have lost Y chromosomes; seven have undergone changes in autosome number. It is not known why such changes are so scarce, nor what particular rearrangements led to the observed diversity. Nonetheless, the cytogenetic data can be used to infer a monophyletic origin of groups possessing derived chromosome numbers or sex chromosomes, and to help resolve species limits.     

Monophyly of Euaesthetinae (Coleoptera: Staphylinidae): phylogenetic evidence from adults and larvae,review of austral genera,and new larval descriptions

Abstract We develop a morphological dataset for the rove beetle subfamily Euaesthetinae comprising 167 morphological characters (135 adult and 32 larval) scored from 30 terminal taxa including 25 ingroup terminals (from subfamilies Euaesthetinae and Steninae) and five outgroups. Four maximum parsimony analyses using different sets of terminals and character sets were run to test the monophyly of (1) Euaesthetinae, (2) Steninae, (3) Euaesthetinae + Steninae, (4) euaesthetine tribes Austroesthetini, Alzadaesthetini, Euaesthetini, Fenderiini and Stenaesthetini, and (5) the ten currently known austral endemic genera together. Analyses of adult and larval character sets separately and in combination recovered the monophyly of Euaesthetinae, Steninae, and both subfamilies together, with strong support. Analysis of 13 ingroup terminals for which complete data were available suggests that monophyly of Euaesthetinae is supported by 19 synapomorphies (13 adult, six larval), of Steninae by 23 synapomorphies (14 adult, nine larval), and of both subfamilies together by 24 synapomorphies (21 adult, three larval). Within Euaesthetinae, only the tribe Stenaesthetini was recovered as monophyletic based on adult characters, and in no analyses were the ten austral endemic genera recovered as a monophyletic group. Phylogenetic relationships among euaesthetine genera were weakly supported, although analyses including adult characters supported monophyly of Octavius and Protopristus separately, and of Octavius + Protopristus, Austroesthetus + Chilioesthetus and Edaphus + Euaesthetus. Steninae may include a third genus comprising two undescribed species probably possessing a ‘stick–capture’ method of prey capture, similar to that in Stenus. These two species formed a strongly supported clade recovered as the sister group of Stenus based on adult characters. Diagnoses and a key to adults are provided for the 15 euaesthetine genera currently known from the austral region (Australia, New Zealand, South Africa and southern South America). Euaesthetine larvae previously were known only for Euaesthetus, and we describe the larvae of nine more genera and provide the first larval identification key for genera of Euaesthetinae.     

Cladistic analysis of morphological characters in the eulophine tribe Cirrospilini (Hymenoptera: Eulophidae)

A total of 56 morphological characters were analyzed for 53 cirrospiline species that represent all of the 17 described genera of the tribe. The other taxa of the Eulophinae included in the analysis were six species of six representative genera in the tribe Eulophini, a species of Elasmus (the only genus comprising the tribe Elasmini), and a species of Trichospilus (unplaced). Trichospilus and two of the six genera of Eulophini examined were placed within Cirrospilini. Monophyly of Cirrospilini (when these two genera of Eulophini and Trichospilus are included) and of the cirrospiline genera for which more than one species were examined was supported, but the relationships between the genera were poorly resolved. An exception was Cirrospilus, the largest genus in the Cirrospilini, monophyly of which was not supported to any extent.     

Phylogenetic analysis of Cyprichromini (Perciformes: Cichlidae) endemic to Lake Tanganyika and validation of the genus <Emphasis Type="Italic">Paracyprichromis</Emphasis>

The phylogenetic relationships among two Paracyprichromis and five Cyprichromis species, included in the Tanganyikan cichlid tribe Cyprichromini, were investigated using morphological features. The previously proposed diagnostic characters of Paracyprichromis are not synapomorphies, because the nonelongated swim bladder is plesiomorphic, the numbers of dorsal and anal fin rays and scales on longitudinal line and around the caudal peduncle overlap with those of Cyprichromis, and these counts and number of vertebrae are all included within the ranges of other Tanganyikan cichlids. The monophyly of Paracyprichromis is supported by a unique condition of infraorbitals to this genus. Additionally, the monophyly of Cyprichromis was reconfirmed by one of the previously proposed diagnostic characters, the presence of an elongated swim bladder.     

Changes in the suprageneric classification of Lasiocampidae (Lepidoptera) based on the nucleotide sequence of gene EF-1α

The nucleotide sequences of nuclear gene EF-1α were determined for 49 species of Lasiocampidae from Eurasia and Africa. Based on these data, the phylogeny of the family was reconstructed using the minimum evolution, maximum parsimony, maximum likelihood, and Bayesian inference methods. The molecular genetic research confirms the monophyly of Malacosominae which is treated as a separate subfamily. The genus Euthrix appears to be paraphyletic. The group of genera similar to Arguda, previously united with Odonestis in the tribe Odonestini, proved to be a separate lineage; contrary to the earlier assumption, the genera do not seem to be related. On the other hand, the genera Argonestis and Odonestis were found to be closely related and therefore were placed in the same tribe. The position of the genus Macrothylacia remains obscure. The genus Stoermeriana de Fr. et Witt is also para- or polyphyletic and consists of several independent lineages whose status remains to be determined. The new classification supports synonymization of Pinarinae with Lasiocampinae. The rank of subfamily is not supported for the Neotropical Macromphaliinae, which is downgraded to a tribe, Macromphaliini stat. n., within Poecilocampinae. The genus Hypopacha, previously considered within Macromphaliinae, is transferred to Poecilocampini; the close relation between Poecilocampini and Macromphaliini is additionally supported by the presence of a member of Poecilocampini in the New World. A new tribe, Argudini Zolotuhin trib. n., is established.     

Larvae of Ceratocanthidae and Hybosoridae (Coleoptera: Scarabaeoidea): study of morphology, phylogenetic analysis and evidence of paraphyly of Hybosoridae

Abstract. Larvae of the scarabaeoid genera Germarostes Paulian, Cyphopisthes Gestro, Paulianostes Ballerio, Ceratocanthus White, Pterorthochaetes Gestro, Madrasostes Paulian, Astaenomoechus Martínez & Pereira (Ceratocanthidae) and Hybosorus Macleay, Phaeochrous Castelnau, and Anaides Westwood (Hybosoridae) are described, keyed and illustrated with fifty‐seven drawings. A phylogenetic analysis of these two families based on larval morphology is presented. Fifty‐four larval morphological and three biological characters from twenty‐seven taxa revealed nineteen equally parsimonious cladograms. The monophyly of (Ceratocanthidae + Hybosoridae) is supported by four unambiguous unique synapomorphies: dorsal medial endocarina on cranium extended anteriorly into frontal sclerite; presence of large membranous spot on apical antennomere; labium dorsally with four pores in centre (secondarily reduced to two pores in some groups); and presence of stridulatory organ on fore‐ and middle legs (secondarily reduced in some groups). Our analysis suggests that the family Hybosoridae is paraphyletic with respect to Ceratocanthidae. The clade comprising the hybosorid genera Hybosorus and Phaeochrous is the sister group of the remaining Hybosoridae plus Ceratocanthidae. It is supported by two unambiguous synapomorphies: two apical antennomeres completely joined and the stridulatory organ represented by seven to nine large teeth anteriorly on the middle leg. The hybosorid genus Anaides is a sister group to the remaining Hybosoridae plus Ceratocanthidae (without Hybosorus and Phaeochrous) and the ceratocanthid genus Germarostes is a sister group to the remaining Hybosoridae plus Ceratocanthidae (without Hybosorus, Phaeochrous and Anaides). The ceratocanthid genera Cyphopisthes, Astaenomoechus, Paulianostes, Pterorthochaetes, and Madrasostes constitute a sister group to the hybosorid genus Cryptogenius and are supported by the presence of two reversions: two dorsal pores on labium and completely reduced stridulatory organs on fore‐ and middle legs.     

Comparative detailed morphology of the Heteroderinae Filip'ev & Schuurmans Stekhoven, 1941, sensu Luc et al. (1988): phylogenetic systematics and revised classification

Taxonomic schemes for the Heteroderinae Filip'ev & Schuurmans Stekhoven, 1941, sensu Luc et al., (1988) have been unstable due to the large number of genera and the paucity of known reliable characters. Reliable characters are essential when using phylogenetic inference in developing a natural classification. Morphological and developmental studies using light, scanning and transmission electron microscopy have revealed the new characters of host response, en face patterns, phasmid structure and female cuticular layers. These techniques also gave us insight into the homoplasy and polarity of many characters, revealed previously undetected character states and clarified misinterpreted character states. A matrix with the 19 most reliable characters is proposed for 20 operational taxonomic units (OTUs) and we employ this matrix for comparing computer generated phylogenetic analyses of the PHYLIP and PAUP packages. PAUP was deemed the more reliable parsimony algorithm for phylogenetic analysis of the Heteroderinae (Fink, 1986; Platnick, 1987). Monophyly of Atalodera + Sherodera + Thecavermiculatus (tribe Ataloderini), and Cactodera + Heterodera + Afenestrata, as well as Punctodera + Globodera + Dolichodera is supported by both programs. Most importantly, analyses strongly support monophyly of all cyst-forming genera (tribe Heteroderini) contrary to previous hypotheses of repeated evolution of the cyst (Wouts, 1985). In addition, monophyly of the Heteroderini with the Ataloderini is demonstrated. PAUP indicates monophyly of Sarisodera + Rhizonema + Bellodera + Hylonema and Ekphymatodera (tribe Sarisoderini new rank). Monophyly of the Sarisoderini was at first only weakly supported, but, subsequently, the reduced width of the submedial lips of second stage juveniles and males was recognized as a synapomorphy which strengthened subsequent PAUP trees and monophyly of the tribe. The present study rejects as paraphyletic or polyphyletic several previously proposed combinations, including Thecavermiculatus sequoiae (versus Rhizonema sequoiae), Sarisodera africana (versus Afenestrata africana), Dolichodera andinus (versus Thecavermiculatus andinus). The question whether T. andinus is a distinct genus, was not resolved due to insufficient data. PAUP supports our previous observations that Cactodera betulae is intermediate in a transformation series between other Cactodera and Heterodera: it also indicates these species as bring monophyletic with Heterodera + Afenestrata, but not with other Cactodera. Although these phylogenetic analyses strongly support some relationships, they indicate unresolved alternative hypotheses for others. Meloidodera (tribe Meloidoderini) and Cryphodera (tribe Cryphoderini) must be investigated for consideration of a possible synapomorphy not included in the present data matrix. Future studies are proposed to more clearly define the monophyly of the Heteroderini, as well as the Sarisoderini. Tests are also proposed to clarify questions of the monophyly of Verutus (tribe Verutini new rank) with the Heteroderinae versus other Tylenchida.     

On the thoracic anatomy of the Madagascan Heterogyrus milloti and the phylogeny of Gyrinidae (Coleoptera)

Gyrinidae is a group of beetles with a unique specialization of swimming on the water surface. Heterogyrus milloti Legros (Heterogyrinae) from Madagascar is a species with various preserved plesiomorphic features. The information on the morphology and biology was very limited until recently, and the thoracic anatomy remained largely unknown. Consequently, the aim of the present study is to describe external and internal thoracic features of Heterogyrus Legros in detail and to interprete them with respect to their phylogenetic and functional significance, with a special focus on the unusual flight apparatus of Gyrinidae. Characters documented with innovative techniques are compared to conditions found in other gyrinid genera and other groups of Adephaga, including characters of other body parts and larvae. A data matrix with 144 characters of adults, larvae and eggs was compiled and analysed cladistically. Gyrinidae excluding Spanglerogyrus Folkers (Heterogyrinae + Gyrininae) is supported by many apomorphies, mainly by a unique locomotor apparatus with paddle‐like middle and hind legs. The results confirm Heterogyrus as the earliest diverging branch in Gyrinidae except Spanglerogyrus, implying a sister‐group relationship between this genus and Gyrininae, a clade comprising Gyrinini, Dineutini and Orectochilini. The presence of an opening between the mesanepisternum and elytra, reduction of the lateral metafurcal arms, loss of the metathoracic M. furcacoxalis lateralis, and modifications of the head, including the dorsal shift of the upper subcomponent of the compound eyes, are synapomorphies of the three tribes. The monophyly of Gyrinini is moderately well‐supported, whereas Orectochilini is strongly supported by different characters including a highly simplified but functioning flight apparatus. A clade comprising Orectochilini and the dineutine genera is suggested by synapomorphies of adults and larvae. The monophyly of Dineutini was supported in a recent study, but not by the characters analysed here. Features of adults, larvae and eggs indicate that Gyrinidae are the sister group to the remaining adephagan families, as suggested in some earlier morphology‐based studies and recent analyses of large molecular datasets.     

Phylogeny of the Agathidiini Westwood (Coleoptera: Leiodidae) and implications for classification and contractile morphology

A cladistic analysis of the tribe Agathidiini Westwood is presented. Agathidiines are slime mould specialists and they are hypothesized to be a monophyletic group consisting of 12 genera (Afroagathidium Angelini & Peck, Agathidium Panzer, Anisotoma Panzer, Besuchetionella Angelini & Peck, Cyrtoplastus Reitter, Decuria Miller & Wheeler, Gelae Miller & Wheeler, Liodopria Reitter, Pseudoagathidium Angelini, Sphaeroliodes Portevin, and Stetholiodes Fall), based on three synapomorphies: epipleuron present to apical third, mesoventrite without longitudinal carina and longitudinal setal lines present on the tibiae. The dataset for phylogenetic analysis comprised 72 characters representing 198 character states derived from adult morphology. These data were analysed using equal weighting and implied weighting (k = 1–6) and supported the monophyly of the tribe based on three unique characters (epipleuron present to apical third, mesoventrite without longitudinal carina, longitudinal setal lines present on tibia) and two homoplastic characters [antennomeres 7–10 (or 6–9) asymmetrical, apical shape of terminal antennomere abruptly tapered]. The topology of IW trees with k = 4–6 was identical with one of three EW trees. Decuria was sister group to the remaining agathidiine genera whereas the following groups were resolved as monophyletic: Anisotoma, Gelae + Liodopria, and Pseudoagathidium (Afroagathidium + Besuchetionella). The clade [Sphaeroliodes rufescens (Agathidium bockshini, Agathidium subcostatum)] was supported in all analyses except for the IW (k = 1) cladogram. The monophyly of Agathidium was not supported at all and was rendered paraphyletic by the placements of Sphaeroliodes, Stetholiodes and the Pseudoagathidium (Afroagathidium + Besuchetionella) clade. Sphaeroliodes is synonymized with Agathidium ( syn.n. ) resulting in two new combinations [A. acuminatus (?vec) and A. rufescens (Portevin)]. Contractability is a complex character composed of several morphological features that have evolved independently within the agathidiine tree. Conglobation (the ability to roll the body into a ball) has arisen at least twice in Agathidiini.     

Phylogeny of the Saprininae reveals interesting ecological shifts in the history of the subfamily (Coleoptera: Histeridae)

A morphological data set for the histerid beetle subfamily Saprininae comprising 95 adult morphological characters scored (multistate coding) from 72 terminal taxa and four outgroups was developed in order to analyse and determine the relationships amongst the genera and subgenera of the Saprininae subfamily. Cladograms were rooted with exemplars of Dendrophilinae (genus Dendrophilus), Bacaniini (genus Bacanius), Abraeinae (genus Chaetabraeus), and Anapleini (genus Anapleus). Parsimony‐based phylogenetic analyses were performed based on the type species of each genus and subgenus of the Saprininae occurring around the world, with the exception of three taxa: Paramyrmetes foveipennis (type species of the genus Paramyrmetes), Satrapister nitens (type species of the genus Satrapister) and Xerosaprinus (Auchmosaprinus) laciniatus (type species of the subgenus Auchmosaprinus) that were not available. In addition, in order to test the monophyly of several questionable genera, multiple exemplars were added in a few cases. The analysis also included an exemplar of an apparently undescribed genus. The results of the analysis confirm the monophyly of the subfamily supported by two unique synapomorphies: (1) presence of sensory structures of the antenna; and (2) presence of the antennal cavity, as well as several other weaker synapomorphies. However, the phylogeny inferred here shows mostly low support for the deeper branches and consequently no major changes in the Saprininae classification are proposed. The presented cladogram is discussed together with its implications for the evolution of the subfamily. The most informative characters and their respective states are outlined. Multiple shifts in lifestyles have evolved during the evolutionary history of the group. Taxa found near the root of the cladogram are mostly nidicolous or myrmecophilous, and inquiliny is presumed to be the plesiomorphic lifestyle of the subfamily. The nidicolous lifestyle has undergone several transformations to other lifestyles and myrmecophily has evolved three times independently during the evolution of the subfamily. Termitoxeny has evolved two times independently in the group whereas ecological adaptation for life in caves has likewise evolved two times independently. The analyses yielded a large clade of predominantly psammophilous taxa; psammophily is thought to have evolved once and has been subsequently lost several times. © 2014 The Linnean Society of London     

Chrysomyinae (Diptera: Calliphoridae) is monophyletic: a molecular systematic analysis

The subfamily Chrysomyinae includes blowflies of considerable ecological and applied importance. Previous extensive morphological investigations have affirmed chrysomyine monophyly, but did not support the monophyly of traditional chrysomyine tribes. Conversely, molecular systematic analyses suggested a para‐ or polyphyletic Chrysomyinae. Conflicting hypotheses have been proposed about the tribe‐level classification, and about the relationships of the obligate bird parasites Protocalliphora Hough and Trypocalliphora Peus. To understand chrysomyine evolution better, we reconstructed phylogenies of the Chrysomyinae based on 2285 bp of combined data from mitochondrial cytochrome oxidase c subunit 1 (COI) and nuclear carbamoylphosphate synthetase (CPS) genes. Maximum parsimony (MP), maximum likelihood (ML) and Bayesian analysis (BA) strongly supported the monophyly of Chrysomyinae and the paraphyly of the tribe Chrysomyini. BA and ML yielded a monophyletic tribe Phormiini, but this was unresolved by MP. A sister‐group relationship between Trypocalliphora and Protocalliphora indicates that obligate bird parasitism evolved once within the Calliphoridae. For the first time all Neotropical genera (Cochliomyia Townsend, Compsomyiops Townsend, Paralucilia Brauer and Bergenstamm, Hemilucilia Brauer and Chloroprocta Wulp) were found to comprise a single lineage, and Chrysomya Robineau‐Desvoidy, traditionally a member of Chrysomyini, was found to be closer to the Phormiini. Similarly, Hemilucilia + Chloroprocta was a monophyletic group. Every genus for which we examined more than one species was monophyletic.     

Phylogenetic relationships of Combretoideae (Combretaceae) inferred from plastid,nuclear gene and spacer sequences

Phylogenetic relationships of the subfamily Combretoideae (Combretaceae) were studied based on DNA sequences of nuclear ribosomal internal transcribed spacer (ITS) regions, the plastid rbcL gene and the intergenic spacer between the psaA and ycf3 genes (PY-IGS), including 16 species of eight genera within two traditional tribes of Combretoideae, and two species of the subfamily Strephonematoideae of Combretaceae as outgroups. Phylogenetic trees based on the three data sets (ITS, rbcL, and PY-IGS) were generated by using maximum parsimony (MP) and maximum likelihood (ML) analyses. Partition-homogeneity tests indicated that the three data sets and the combined data set are homogeneous. In the combined phylogenetic trees, all ingroup taxa are divided into two main clades, which correspond to the two tribes Laguncularieae and Combreteae. In the Laguncularieae clade, two mangrove genera, Lumnitzera and Laguncularia, are shown to be sister taxa. In the tribe Combreteae, two major clades can be classified: one includes three genera Quisqualis, Combretum and Calycopteris, within which the monophyly of the tribe Combreteae sensu Engler and Diels including Quisqualis and Combretum is strongly supported, and this monophyly is then sister to the monotypic genus Calycopteris; another major clade includes three genera Anogeissus, Terminalia and Conocarpus. There is no support for the monophyly of Terminalia as it forms a polytomy with Anogeissus. This clade is sister to Conocarpus. Electronic Publication     

Phylogeny of North American Tolypella (Charophyceae,Charophyta) based on plastid DNA sequences with a description of Tolypella ramosissima sp. nov.

Characeae (Charophyceae, Charophyta) contains two tribes with six genera: tribe Chareae with four genera and tribe Nitelleae, which includes Tolypella and Nitella. This paper uses molecular and morphological data to elucidate the phylogeny of Tolypella species in North America. In the most comprehensive taxonomic treatment of Characeae, 16 Tolypella species worldwide were subsumed into two species, T. intricata and T. nidifica, in two sections, Rothia and Tolypella respectively. It was further suggested that Tolypella might be a derived group within Nitella. In this investigation into species diversity and relationships in North American Tolypella, sequence data from the plastid genes atpB, psbC, and rbcL were assembled for a broad range of charophycean and land plant taxa. Molecular data were used in conjunction with morphology to test monophyly of the genus and species within it. Phylogenetic analyses of the sequence data showed that Characeae is monophyletic but that Nitelleae is paraphyletic with Tolypella sister to a monophyletic Nitella + Chareae. The results also supported the monophyly of Tolypella and the sections Rothia and Tolypella. Morphologically defined species were supported as clades with little or no DNA sequence differences. In addition, molecular data revealed several lineages and a new species (T. ramosissima sp. nov.), which suggests greater species diversity in Tolypella than previously recognized.     

Osteology of <Emphasis Type="Italic">Ischikauia steenackeri</Emphasis> (Teleostei: Cypriniformes) with comments on its systematic position

The lakeweed chub Ischikauia steenackeri is a medium-sized, herbivorous fish and the sole extant member of the genus Ischikauia, which is endemic to Lake Biwa and the Yodo River drainage, Japan. In order to clarify its systematic position, the skeletal anatomy of I. steenackeri is described and its relationships with related genera are discussed. The present data suggest the monophyly of Ischikauia and seven cultrine genera (Culter, Chanodichthys, Megalobrama, Sinibrama, Hemiculter, Toxabramis, and Anabarilius) based on a unique character, the metapterygoid elongated dorsally. Additionally, our data suggest that Ischikauia is closely related to Culter, Chanodichthys, Megalobrama, and Sinibrama. This relationship is supported by three synapomorphies that are common to them: a narrow third infraorbital, dorsal extension of the third supraneural, and a large quadrate foramen.     

Phylogeny of the flyingfish family Exocoetidae (Teleostei, Beloniformes)

The phylogeny of the flyingfish family Exocoetidae is studied cladistically, using 41 morphological characters encompassing early life history, and external and internal features. The monophyly of the family is supported by 10 synapomorphies. Within the family,Oxyporhamphus is the sister group to all other genera, the monophyly of the latter being defined by 10 synapomorphies.Fodiator is the sister group of genera characterized by the presence of chin barbels in juveniles.Parexocoetus is the sister group ofExocoetus, Cypselurus, Prognichthys andHirundichthys, the latter being defined by four synapomorphies. In the latter group,Exocoetus is the sister group of the other three genera. The phylogeny of the Exocoetidae is characterized by the stepwise upgrading of gliding capability, with sequential modifications of the caudal, pectoral and pelvic fins. The subfamily Oxyporhamphinae is resurrected.     

Foonchewia guangdongensis gen. et sp. nov. (Rubioideae: Rubiaceae) and its systematic position inferred from chloroplast sequences and morphology

Abstract The new species, Foonchewia guangdongensis R. J. Wang & H. Z. Wen and the new monotypic genus Foonchewia R. J. Wang (Rubioideae, Rubiaceae), are described from eastern Guangdong, China. It is characterized by its subshrub habit, pentamerous and heterostylous flowers, 2‐1ocular ovary with many ovules, and apically dehiscent capsules with numerous angulated seeds. Phylogenetic analysis of four chloroplast DNA regions (rbcL, rps16, ndhF, and atpB‐rbcL) revealed that the new genus is nested in the Spermacoceae alliance and is sister to Dunnia. Morphological comparison between these two genera indicated that they had few synapomorphies; it was therefore inappropriate to classify the new genus in the existing tribe Dunnieae, and a new tribe, Foonchewieae R. J. Wang, is accordingly proposed.     

Phylogenetic study of the Characinae (Teleostei: Characiformes: Characidae)

The Characinae is a subunit of the Characidae of special significance in including Charax, the type genus of the family and the order Characiformes. Twelve genera and 79 species have been traditionally assigned to the Characinae, but the subfamily still lacks a phylogenetic diagnosis. Herein, a data matrix including 150 morphological characters and 64 taxa (35 species representing all genera of the Characinae and 29 included in other lineages within the Characiformes) was submitted to two cladistic analyses that differ in the inclusion/exclusion of Priocharax due to the difficulty of coding most of the character states in the miniature species of this genus. Both analyses resulted in a non‐monophyletic Characinae and this subfamily is herein restricted to only seven of the original 12 genera forming the clade (Phenacogaster((Charax Roeboides)(Acanthocharax(Cynopotamus(Acestrocephalus Galeocharax))))), which is supported by ten non‐ambiguous synapomorphies and is more closely related to other genera of the Characidae than those traditionally placed in the subfamily. A second clade includes the members of the tribe Heterocharacini (Lonchogenys(Heterocharax Hoplocharax)) as the sister‐group of Gnathocharax, supported by seven non‐ambiguous synapomorphies. This clade is more closely related to a taxon formed by Roestes and Gilbertolus based on seven non‐ambiguous synapomorphies. Results do not corroborate a close relationship between Roestes–Gilbertolus and the Cynodontinae. Inclusion of the genus Priocharax suggests that it is related more closely to the Heterocharacini, but the profound modifications in its anatomy possibly related to ontogenetic truncations obscure a better understanding of its relationships. A new classification of the Characinae and the Heterocharacinae is proposed. © 2012 The Linnean Society of London, Zoological Journal of the Linnean Society, 2012, 165 , 809–915.     

Phylogeny and systematics of the tribe Sonerileae (Melastomataceae) in Africa: A revised taxonomic classification

The tribe Sonerileae in tropical Africa and Madagascar is a morphologically diverse lineage that consists of 239 species in 10 genera. In this study, we present the first in-depth phylogenetic analysis of African Sonerileae to test monophyly of the currently recognized genera. Phylogenetic analyses were performed using sequence data from two nuclear (nrITS and nrETS) and three plastid loci (accD-psaI, ndhF and psbK-psbL). Sampling consisted of 140 accessions including 64 African, 27 Malagasy, 46 Asian, and three neotropical Sonerileae together with a broad outgroup sampling (105 spp.). Phylogenetic relationships were inferred using maximum likelihood and Bayesian inference approaches, and a careful reassessment of morphological characters was carried out. Our results neither support the monophyly of the Old World nor African Sonerileae. The monospecific African genus Benna is partially supported as sister to Phainantha, one of the basal neotropical lineages, while African and Malagasy Medinilla are nested among the SE Asian genera. Gravesia (116 spp.), the most species-rich and morphologically diverse genus in Madagascar, is recovered as monophyletic. The African genera of Sonerileae Calvoa, Dicellandra, and Preussiella form well-supported clades. In contrast, Amphiblemma (including Amphiblemma molle) and Cincinnobotrys s.l. (including Cincinnobotrys felicis) are not monophyletic. To accommodate the caulescent C. felicis we propose reinstatement of the monospecific genus Bourdaria. For the distinctive A. molle a new genus Mendelia is described. Calvoa hirsuta is designated here as the type of genus Calvoa, lectotypes are designated for Medinilla engleri and Veprecella lutea, and a neotype is designated for Preussiella kamerunensis.