Calystegines as chemotaxonomic markers in the Convolvulaceae

An extended GC-MS study of 129 convolvulaceous species belonging to 29 genera (all 12 tribes) including the results of a previous survey (65 spp.) revealed the occurrence of one to six polyhydroxy alkaloids of the nortropane type (calystegines) in 62 species belonging to 22 genera of all tribes except the unique parasitic Cuscuteae. The large genus Ipomoea turned out to comprise calystegine-positive species in at least eight out of ten sections checked. The number of the calystegines used as reference compounds has been increased from seven (previous survey) to 11 (present study). Furthermore, the results concerning these additional four alkaloids could also be completed for all species of the previous survey. The plant material (epigeal vegetative parts and/or roots, flowers, fruits/seeds) was obtained from collections in the wild from a wide range of tropical, subtropical, and temperate locations of all continents as well as from cultivation in the greenhouse. All plant organs turned out to be potential locations for the occurrence of these metabolites though they are detectable often only in certain organs of a given species. Three genera (Cuscuta, Operculina, Polymeria) might have lost the ability to synthesize these plesiomorphic characters in the course of the evolution since the examination of several different organs and/or provenances of five species each failed to show calystegines as constituents. Nevertheless, the present data clearly demonstrate that the occurrence of calystegines is an almost consistent trait in the Convolvulaceae in principle, from basal to most advanced tribes.     

Wood anatomy of the subfamily Crotonoideae (Euphorbiaceae s.s.) from India: systematic implications with special reference to the taxonomic delimitation of Givotia and Vernicia

The wood anatomy of 15 representative species belonging to 12 genera of nine tribes of the subfamily Crotonoideae (Euphorbiaceae) are comprehensively described with focus on systematic implications. In addition, ecological and evolutionary aspects are evaluated. An identification key to the species based on wood anatomical features is presented. The wood microstructure of the tribes was found to be considerably heterogeneous reflecting an unnatural classification of the subfamily. However, the results confirm the generic relationship within subtribe Aleuritinae and tribe Ricinodendreae. Vernicia and Givotia may be recognized based on wood anatomical and morphological characters. The tribes Micrandreae and Adenoclineae have considerable similarity in wood anatomy. The wood structure of the monogeneric tribes Trigonostemoneae and Geloneae idicate a close relationship with the tribe Crotoneae.     

Serotaxonomy and systematic relationships of the genus Adenocarpus (Genisteae – Fabaceae)

The storage proteins extracted from the seeds of five species of the genus Adenocarpus and of four subspecies or varieties of the type species A. complicates were studied serologically and compared with the homologous proteins extracted from 20 other species of Genisteae and allied tribes. All taxa of Adenocarpus reacted strongly with an antiserum to A. complicates ssp. complicates; only slight differences were observed between subspecies and between species. Adenocarpus was shown to be isolated from all other Genisteae. However, it was more similar to the Genisteae than to species of other tribes. The highest similarity toward Adenocarpus was presented by Argyrolobium , by some primitive unspecialized genera (Laburnum, Cytisophyllum) , and by such isolated genera as Cytisanthus, Spartium, Echinospartum. Retama and Lupinus were most dissimilar. It is concluded that Adenocarpus , a very uniform and isolated genus, belongs to the Genisteae; it shares many characters with the bulk of primitive genera of the Genisteae; its evolutionary line is independent from all others, but is not very distant from that of Argyrolobium.     

Floral structure and evolution in the Anacardiaceae

WANNAN, B. S. & QUINN, C. J, 1991. Floral structure and evolution in the Anacardiaceae. Carpel morphology and anatomy is investigated in 17 genera and carpellode morphology in 12 genera. There is an evolutionary sequence in the family from poorly differentiated, nearly apocarpous gynoecia towards syncarpous gynoecia with clearly defined stigmata, styles and ovaries. There has also been marked reduction culminating in pseudomonomery. The carpellodes of the male flowers appear more conservative, and provide evidence of affinities between genera with quite different fertile gynoecia. The characters have been polarized using Burseraceae as a sister group. Data from these sources, as well as from pericarp anatomy, wood anatomy and biflavonoid content indicate that the long standing intrafamilial classification into five tribes is artificial, and that the two small satellite families, Blepharocaryaceae and Julianiaceae should be included in the family. A large monophyletic group is recognized comprised of essentially four of the existing tribes (Anacardiëae, Dobineëae, Semecarpeae, Rhoëae), as well as the two satellite families. This group incorporates two subgroups of more closely allied genera. The remaining genera (mostly Spondiadeae) are very diverse, and for the present are placed in an artificial group characterised by a set of plesiomorphs. Relationships within this group must be resolved before a satisfactory taxonomy of the family can be achieved.     

Ovules and seeds in Acalyphoideae (Euphorbiaceae): structure and systematic implications

Acalyphoideae, the largest subfamily of Euphorbiaceae, are investigated with respect to ovule and seed structure on the basis of 172 species of 80 genera in all 20 tribes of Acalyphoideae sensu Webster. All species of Acalyphoideae examined have bitegmic ovules with a non-vascularized inner integument. However, noticeable differences exist among and sometimes within the genera in the thickness of the inner and outer integument, the presence or absence of vascular bundles in the outer integument, whether ovules are pachychalazal or not, the presence or absence of an aril, seed coat structure (in terms of the best-developed mechanical cell-layer), and the shape of cells constituting the exotegmen. For the latter two characters, two different types of seed coat (i.e., "exotegmic" and "exotestal") and three different types of exotegmic cell (i.e., palisadal, tracheoidal and ribbon-like) were distinguished. Comparisons showed that three tribes Clutieae, Chaetocarpeae and Pereae are distinct from the other Acalyphoideae as well as from the other Euphorbiaceae in having an exotestal seed coat with a tracheoidal exotegmen. The tribe Dicoelieae is also distinct from the other Acalyphoideae in having an exotegmic seed that is composed of ribbon-like cells of exotegmen (i.e., cells both longitudinally and radially elongated, sclerotic and pitted). The tribe Galearieae, which should be treated as a distinct family Pandaceae, is also distinct from the other Acalyphoideae in having an exotegmic seed with a tracheoidal exotegmen (i.e., cells longitudinally elongated, sclerotic and pitted). The remaining genera of Acalyphoideae always have an exotegmic seed with a palisadal exotegmen (i.e., cells radially elongated, sclerotic and pitted). The shared palisadal exotegmen supports the close affinity of Acalyphoideae (excluding five tribes) with Crotonoideae and Euphorbioideae. Within the remaining genera of Acalyphoideae, a significant diversity is found in ovule and seed morphology with respect to the thickness of the inner and outer integument, the size of chalaza, vascularization of an outer integument and an aril.     

Derivation and dispersal of Acacia (Leguminosae), with particular reference to Australia, and the recognition of Senegalia and Racosperma

The morphology of seedlings, leaves, flowers and inflorescences, anatomy of the pod, the occurrence of extra-floral nectaries, free amino acids of the seeds, flavonoid compounds in heartwoods, cyanogenic compounds and porate, colporate and extraporate pollen, and susceptibility to rusts, all indicate that three genera, Acacia Miller, Senegalia Raf. and Racosperma Martius, should be recognized. These correspond to currently accepted subgenera of Acacia. The size of these more narrowly circumscribed genera is in keeping with the size of genera of other tribes of low diversity in Leguminosae. Acacia and Senegalia arose independently from the Ingeae, with Racosperma being derived from Senegalia. Section Filicinae is more advanced than section Senegalia of Senegalia , and sections Racosperma and Pukhella , both with at least some species with bipinnate foliage, are the most advanced of Racosperma , while the other sections Pleurinervia and Lycopodiifolia have only phyllodinous species. Long-range dispersal of Racosperma from the Australian region has occurred, but the broad pattern of distribution is interpreted in terms of plate tectonics. Racosperma was present in Australia in the late Cretaceous but did not become widespread until the general drying of the continent in the Miocene. The flora of SW Australia has been isolated from the rest of the continent by climatic barriers since the late Tertiary and has a high proportion of endemic species. Barriers to plant migration in the east have operated only intermittently and there is no area comparable in endemism to the southwest.     

Female flowers and systematic position of Picrodendraceae (Euphorbiaceae s.l., Malpighiales)

This is the first comparative study of floral structure of the recently established new family Picrodendraceae (part of Euphorbiaceae s.l.) in Malpighiales. Nine species of eight (out of ca. 28) genera were studied. Female flowers are mainly completely trimerous, and in such flowers the perianth consists of one or two whorls of sepals. A floral disc (which probably functions as a nectary) is mostly present. The free parts of the carpels are simple (unbranched) in all ten species studied. Each carpel contains two crassinucellar, anatropous or hemitropous, epitropous (antitropous) ovules, which are covered by a large obturator. The inner integument is thicker than the outer (equally thick in two species studied), and commonly both integuments form the micropyle. In mature ovules the vascular bundle commonly branches in the chalaza, with the branches extending to the base of the inner integument but not entering it. A nucellar cap and, less often, a nucellar beak is formed. Floral structure supports the close relationship of Picrodendraceae with Phyllanthaceae and Euphorbiaceae s.str. within Malpighiales, as suggested (but not yet strongly supported) by some recent published molecular analyses. These three families share a unique combination of characters, including (1) unisexual, apetalous trimerous flowers, (2) crassinucellar ovules with a nucellar beak, (3) a large obturator, and (4) explosive fruits with carunculate seeds.     

大戟科植物分类的数值分析

根据大戟科216个分类性状的分布,采用欧氏距离系数一类平均法对Webster(1994)广义大戟科49个族或亚族进行聚类分析。结果表明,现行的大戟科分类系统中,大多数族和亚族水平的分类基本合理,而Galearieae族的系统位置和五月茶族Antidesmeae等亚族的划分出现较大矛盾。该系统中未包含的方鼎木属Archileptopus,应与叶下珠族的Pseudolachnostylidillae亚族接近。     

Phylogenetic utility of the major opsin in bees (Hymenoptera: Apoidea): a reassessment

Major opsin (LW Rh) DNA sequence has been reported to provide useful data for resolving phylogenetic relationships among tribes of corbiculate bees based on analyses of 502 bp of coding sequence. However, the corbiculate tribes are believed to be of Cretaceous age, and strong support for insect clades of this age from small data sets of nucleotide sequence data has rarely been demonstrated. To more critically assess opsin's phylogenetic utility we generated an expanded LW Rh data set by sequencing the same gene fragment from 52 additional bee species from 24 tribes and all six extant bee families. Analyses of this data set failed to provide substantial support for monophyly of corbiculate bees, for relationships among corbiculate tribes, or for most other well-established higher-level relationships among long-tongued bees. However, monophyly of nearly all genera and tribes is strongly supported, indicating that LW Rh provides useful phylogenetic signal at lower taxonomic levels. When our expanded LW Rh data set is combined with a morphological and behavioral data set for corbiculate bees, the results unambiguously support the traditional phylogeny of the corbiculate bee tribes: (Euglossini + (Bombini + (Meliponini + Apini))). This implies a single origin of advanced eusocial behavior among bees rather than dual origins, as proposed by several recent studies.     

PATTERNS OF STAMEN VASCULATURE IN THE ARACEAE

A survey of the three-dimensional organization of stamen vasculature in 100 genera and over 350 species of Araceae was made using clearings. The Araceae exhibit highly varied stamen vasculature, with three main patterns: 1) vascular bundles unbranched, 1–3 per stamen, 2) forked bundles in some or all stamens, 3) anastomosing vascular systems with several to many bundles entering a single stamen. Three major groups of taxa in the family can be recognized on the basis of their predominant pattern of stamen vasculature. Virtually all genera with bisexual flowers (most Pothoideae, Monsteroideae, Calloideae, Lasieae) have unbranched bundles, one per stamen, except two to three in some species of Holochlamys, Spathiphyllum, and Scindapsus. Forked stamen bundles are virtually restricted to and occur nearly throughout the monoecious Lasioideae, Philodendroideae, Colocasioideae and among certain Aroideae (sensu Engler), including tribes Arophyteae, Spathicarpeae (Asterostigmateae) and Protareae. No forked bundles were found in tribe Areae (Aroideae), except Theriophonum indicum or any Araceae with bisexual flowers, except two species of Cyrtosperma. Anastomosing systems are virtually limited to members of tribe Areae with larger stamens, such as Arum, Helicodiceros, Eminium and Dracunculus species. A similar pattern occurs in some Amorphophallus, but other patterns occur as well. The distributions of forked bundles and anastomosing systems in the family are notable because they are both highly congruent with Philodendroideae-Colocasioideae, and Aroideae, respectively, in Grayum's new system for the family. Virtually all of the genera with forked bundles are grouped together in the Philodendroideae-Colocasioideae. All of the genera with anastomosing systems are in the Areae, including the complex and variable Amorphophallus, which has an uncertain systematic placement.     

Vicariance biogeography and terrane tectonics in the South Pacific: analysis of the genus Abrotanella (Compositae)

The species of Abrotanella (Compositae) form mats and cushions a few centimetres high and up to a metre or more in diameter. The flowers are less complex than those of most Compositae and lack a pappus, the usual means of dispersal in the family. There are 20 species, all restricted to mountains of Australasia and southern South America. The putative affinities of Abrotanella involve several tribes of Compositae and the genus is not considered derived within the family. A comparative analysis of areas of endemism in Abrotanella shows clear patterns of vicariance and disjunction shared with many plants and animals, and longdistance dispersal is rejected as an explanation. Abrotanella and the three genera related to it are all restricted to lands bordering the Pacific. Areas previously accepted as areas of endemism, such as New Guinea, Tasmania, New Zealand and southern South America, are shown to be polyphyletic complexes, rather than simple areas. Use of such areas in area cladograms leads to the erroneous interpretation of taxa-area relations as incongruent. Distributions of the taxa in Abrotanella are correlated with tectonic features such as plate margins, transform faults and fracture zones, and processes such as continental rifting, terrane accretion, granite emplacement and orogeny. Abrotanellapatearoa sp. nov., a high-alpine cushion-plant, is described from mountains of eastern Central Otago: Rock and Pillar Range, Lammerlaw Range, Umbrella Mountains and Garvie Mountains.     

Phylogeny and biogeography of Neotropical spittlebugs (Hemiptera: Cercopidae: Ischnorhininae): revised tribal classification based on morphological data

The spittlebug family Cercopidae is currently divided into two subfamilies: the paraphyletic Old World Cercopinae and the monophyletic New World Ischnorhininae. The most recent classification scheme proposed by Fennah in 1968 divided the New World Cercopidae into four tribes: Tomaspidini, Ischnorhinini, Hyboscartini and Neaenini. Herein we present a phylogenetic analysis of Ischnorhininae using 108 morphological characters and including 53 of the 59 recognized genera, to evaluate the tribal‐level classification and understand the processes underlying the current distributional patterns of these genera. We found significant support for the monophyly of many Neotropical genera, but Fennah's tribal classification is revised because tribes Neaenini, Ischnorhinini and Tomaspidini were recovered as polyphyletic. Hyboscartini was synonymized with Tomaspidini. A taxonomic key to tribes and genera of Neotropical spittlebugs is provided based mostly on recovered apomorphies. The biogeographical analysis suggests a Neotropical origin of ischnorhinines, more specifically in northwestern South America. This was possibly coincident spatially and temporally with the origin of grasses, with ancestral range expansions southward to the Amazonian and Paraná regions, and posterior vicariant events, possibly related to the expansion of forests in the Chacoan region, the South America diagonal of open formations. Dispersals to the Chacoan region and to the Nearctic region are hypothesized to have occurred only within genera. In the Chacoan region it is associated with more recent events, such as the diversification of C4 grasses and establishment of the savannas and seasonally dry forests.     

Phenetic and cladistic relationships among tenebrionid beetles (Coleoptera)

Abstract. The higher classification of Tenebrionidae is analysed using numerical phenetic, numerical cladistic and traditional Hennigian methods. In all, eighty characters are examined for about 335 taxa; definitive analyses are made on combinations of eighteen to seventy characters for thirty-three OTUs. At lower levels of relationship (genera and closely related tribes) phenetic and cladistic classifications are shown to be congruent, but at higher levels (tribes and subfamilies) there is marked discordance with phenetic results being more stable. A consensus classification is more similar to the Hennigian cladogram than is any single computer generated cladogram. Two main tribal groups – the Lagrioid and Tenebrionoid groups – are suggested which differ in defensive glands, female anatomy, wing and mouthpart morphology, larval characters and other features. The Tenebrionoid group consists of three main subdivisions – the tenebrionine, coelometopine and diaperine lineages. Changes in classificatory position are recommended for eighty-seven genera and tribes (listed in Appendix E) and implied for numerous others.     

Phylogeny,classification and biogeography of bombyliine bee flies (Diptera,Bombyliidae)

The Bombyliinae comprises over 1100 described species in 73 known genera distributed worldwide. It is one of the largest subfamilies of bee flies (Diptera: Bombyliidae). We present the first phylogenetic hypothesis for this subfamily, based on 157 adult morphological characters scored for 123 species representing 60 genera, including all the tribes of Bombyliinae, and the related subfamilies Lordotinae and Toxophorinae. Four most parsimonious trees were generated from our analysis under equal weighting schemes. The monophyly of Bombyliinae is supported, and Lordotinae is sister to the Bombyliinae. Within Bombyliinae, Conophorini is sister to the remaining tribes. Five previously recognized tribes are revised and four new tribes are erected. We placed almost all genera in our tribal classification, based on our phylogenetic results and available character evidence. The genus Parabombylius is proposed as a synonym of Bombylius. The Gondwanan origin for the major lineages of Bombyliinae is strongly indicated by our biogeographic analysis which reconstructs ancestral areas. This published work has been registered in ZooBank, http://zoobank.org/urn:lsid:zoobank.org:pub: 1EC5C827‐34D5‐4A95‐BA78‐4ACF457F6D40.     

Molecular Phylogenetics and Biogeography of the Caribbean-Centered <Emphasis Type="Italic">Croton</Emphasis> Subgenus <Emphasis Type="Italic">Moacroton</Emphasis> (Euphorbiaceae s.s.)

Initial molecular phylogenetic studies established the monophylly of the large genus Croton (Euphorbiaceae s.s.) and suggested that the group originated in the New World. A denser and more targeted sampling of Croton species points to a South American origin for the genus. The nuclear and chloroplast genomes indicate a different rooting for the phylogeny of Croton. Although we favor the rooting indicated by the chloroplast data our conclusions are also consistent with the topology inferred from the nuclear data. The satellite genera Cubacroton and Moacroton are embedded within Croton. These two genera are synonimized into Croton and a new subgenus, Croton subgenus Moacroton, is circumscribed to include them and their allied Croton species. Croton subgenus Moacroton is morphologically characterized by a primarily lepidote indumentum, bifid or simple styles, and pistillate flowers with sepals that are connate at the base. This newly circumscribed subgenus is found from North America to South America, and in contrast to the majority of Croton species most of its members are found in mesic habitats. The group is most diverse in the greater Caribbean basin. A molecular clock was calibrated to the phylogeny using the available Euphorbiaceae fossils. The timing and pattern of diversification of Croton is consistent with both the GAARlandia and Laurasian migration hypotheses. A single species, Croton poecilanthus from Puerto Rico, is placed incongruently by its nuclear and chloroplast genomes. The possibility of this species being of hybrid origin is discussed.      

Mitochondrial phylogeny of Arvicolinae using comprehensive taxonomic sampling yields new insights

Comprehensive taxonomic sampling can vastly improve the accuracy of phylogenetic reconstruction. Here, we present the most inclusive phylogenetic analysis of Arvicolinae (Mammalia, Rodentia) to date, combining all published cytochrome  b gene sequences of greater than 1097 bp and new sequences from two monotypic genera. Overall, the phylogenetic relationships between 69 species of voles and lemmings, representing 18 genera and 10 tribes, were studied. By applying powerful modern approaches to phylogenetic reconstruction, such as maximum likelihood and Bayesian analysis, we provide new information on the early pulse of evolution within the Arvicolinae. While the position of two highly divergent lineages, Phenacomys and Ondatra , could not be resolved, the tribe Lemmini, appeared as the most basal group of voles. The collared lemmings (Dicrostonychini) grouped together with all of the remaining tribes. The two previously unstudied monotypic genera Dinaromys and Prometheomys form a moderately well-supported monophyletic clade, possibly a sister group to Ellobius (Ellobiusini). Furthermore, with one exception, all tribes ( sensu Musser & Carleton, 2005) proved to be monophyletic and can thus be regarded as meaningful evolutionary entities. Only the tribe Arvicolini emerged as paraphyletic in both analyses because of the unresolved phylogenetic position of Arvicola terrestris . Steppe voles of the genus Lagurus were solidly supported as a sister group to the Microtus and allies clade.  © 2008 The Linnean Society of London, Biological Journal of the Linnean Society , 2008, 94 , 825–835.