Phylogeny of the Proteaceae based on atpB and atpB-rbcL intergenic spacer region sequences

1998 ◽  
Vol 11 (4) ◽  
pp. 301 ◽  
Author(s):  
Sara B. Hoot ◽  
Andrew W. Douglas

Parsimony analyses were conducted for 46 genera representing all subfamilies and tribes within Proteaceae using two chloroplast sequences: the gene atpB and the noncoding spacer region between atpB and rbcL. The spacer region was more variable than atpB and provided insertion and deletion data as well as nucleotide substitutions. The atpB and spacer region data sets were highly congruent (as indicated by the partition homogeneity test) and were analysed separately and combined. Both unweighted and weighted character states (3 : 1 correction for transition bias) for the atpB data resulted in very similar strict consensus trees. In addition, the large subfamilies Proteoideae and Grevilleoideae were analysed separately, using appropriate outgroups determined by the analyses with complete sampling. The results from the combination of data were better resolved and supported than the results from each separate data set, although the Grevilleoideae were highly unresolved in all analyses. Most subfamilies in the Proteaceae were essentially monophyletic, but most tribes and subtribes were not. Bellendena is weakly supported as the sister group to all remaining members of the Proteaceae. Monotypic Eidotheoideae is well supported as a member of Proteoideae. Carnarvonioideae and Sphalmioideae are strongly supported as closely allied to the Grevilleoideae, but their positions in relation to this subfamily are unresolved. Other unusual alliances supported by our molecular data are: Isopogon–Adenanthos–Leucadendron–Protea, Petrophile–Aulax, Cardwellia–Euplassa–Gevuina, and Opisthiolepis–Buckinghamia–Grevillea. The tree resulting from the combined data showed limited congruence with morphological characters (flower pairs, stylar pollen presentation, and ovule number). Congruence with chromosome number was minimal, but our tree does support previous hypotheses of multiple aneuploidy and chromosome doubling events. The African and South American genera included in our analysis are dispersed among various clades with taxa from Australia and Asia, suggesting a former Gondwanian distribution for Proteaceae.

2001 ◽  
Vol 32 (2) ◽  
pp. 205-216 ◽  
Author(s):  
John W.H. Trueman ◽  
Rita Marullo ◽  
Laurence A. Mound

AbstractThe subfamily Panchaetothripinae, comprising 35 genera and 98 species, includes several pest species of which the most notorious is the greenhouse thrips, Heliothrips haemorrhoidalis. In an attempt to establish the sister-group of Heliothrips, the relationships of this genus to 31 of the other genera in the subfamily were examined cladistically, using 35 parsimony-informative morphological characters. The analysis indicated that there was no support for two of the three tribes into which this subfamily is customarily arranged, the Monilothripini and the Panchaetothripini, but weak support for the tribe Tryphactothripini. No clear sister-group relationship could be identified for the New World genus Heliothrips, although it grouped with three old world genera Australothrips, Retithrips and Rhipiphorothrips. It is concluded that a morphological data set is not capable of producing a robust phylogeny of the Panchaetothripinae, and that the subject requires re-examination using molecular data.


2009 ◽  
Vol 40 (1) ◽  
pp. 3-41 ◽  
Author(s):  
Detlef Bernhard ◽  
Rolf Beutel ◽  
Albrecht Komarek ◽  
Ignacio Ribera

AbstractAn extensive combined data set comprising 160 morphological characters of adults and immature stages of Hydrophiloidea and sequences of six different genes were analysed using parsimony and a Bayesian approach. Analyses were carried out with equal weight for individual morphological and molecular characters, and alternatively with approximately equivalent weight for the entire partitions, i.e., 147 informative morphological characters × 9.5 ≈ 1383 informative molecular characters. With the former approach some conventional groups such as the histeroid lineage (Histeridae and Sphaeritidae), Helophorinae and Sphaeridiinae were recovered. However, the branching pattern as a whole is strongly in contrast to the results of previous studies. The results obtained with the modified weighting scheme (9.5:1) conform more to morphology based analyses. The monophyly of Hydrophiloidea, Histeridae + Sphaeritidae, Epimetopinae + Georissinae, Helophorinae, Sphaeridiinae and of the hydrophiline-sphaeridiine lineage is supported in the parsimony analysis. Spercheinae is placed as sister group of all the remaining hydrophiloid groups and a clade is formed by the subfamilies Epimetopinae, Georissinae, Hydrochinae and Helophorinae. In the Bayesian analysis the monophyly of Hydrophilidae is supported. Georissinae form a clade with Hydrochinae, and Epimetopinae are placed as sister group of a clade comprising Spercheinae + the hydrophiline-sphaeridiine lineage. Berosus is placed as the sister group of the remaining groups of Hydrophilinae-Sphaeridiinae in both analyses, and Sphaeridiinae are always nested within a paraphyletic Hydrophilinae. The divergent results of the different analyses show that important questions in the phylogeny of Hydrophiloidea such as for instance the placement of Spercheinae are still open.


Author(s):  
T.S. Kemp

The vast majority of living and fossil mammals are placentals. Today there are about 4,400 species, which are traditionally organised into 18 Orders, with an extra one if the Pinnipedia are separated from the Carnivora, and a twentieth if the recently extinct Malagasy order Bibymalagasia is recognised as such. There have been many attempts to discover supraordinal groupings from amongst these Orders based on morphological characters, though few proposals have been universally accepted. It is only with the advent of increasingly large sets of molecular sequence data in the last few years that a reasonably robust resolution looks imminent, although these contemporary analyses are remarkably and controversially at odds with the traditional ones. Novacek et al. (1988) summarised the then current situation regarding supraordinal classification of placentals, a time at which morphology was still dominant but molecular data was at the threshold of significance. They accepted a basal group Edentata that combined the Xenarthra of the New World with the Pholidota of the Old, based on a few cranial characters, loss of the anterior teeth, and reduction of the enamel of the remaining ones. This left the rest of the living placentals as a monophyletic group Epitheria, sharing such apparently minor characters as the shape of the stapes bone in the ear. They found very little resolution within the Epitheria, and concluded that there was a polychotomy of no less than nine lineages arranged as a ‘star’ phylogeny. No remnant of the previously recognised taxon Ferungulata, created by Simpson (1945) for the Carnivora plus the ungulate orders Artiodactyla, Perissodactyla, Proboscidea, Hyracoidea, Sirenia, and Tubulidentata remained. On the other hand, three supra ordinal taxa of earlier authors did survive. One was Gregory’s (1910) Archonta, consisting of generally conservative forms and by now composed of the Primates, Dermoptera, Scandentia, and Chiroptera, but excluding the Lipotyphla. The second was Glires, originating with Linnaeus (1758) and widely accepted ever since, for the Rodentia and Lagomorpha; Novacek et al. (1988) tentatively placed the Macroscelidea as the sister-group of the Glires. The third supraordinal taxon recognised was, like Glires, well-established if not universally accepted.


Zootaxa ◽  
2007 ◽  
Vol 1423 (1) ◽  
pp. 1-26 ◽  
Author(s):  
JEFFREY H. SKEVINGTON ◽  
CHRISTIAN KEHLMAIER ◽  
GUNILLA STÅHLS

Sequence data from 658 base pairs of mitochondrial cytochrome c oxidase I (cox1) were analysed for 28 described species of Pipunculidae (Diptera) in an effort to test the concept of DNA Barcoding on this family. Two recently revised but distantly related pipunculid lineages with presumed different evolutionary histories were used for the test (Clistoabdominalis Skevington, 2001 and Nephrocerus Zetterstedt, 1838). An effort was made to test the concept using sister taxa and morphologically similar sibling species swarms in these two genera. Morphological species concepts for Clistoabdominalis taxa were either supported by cox1 data or found to be too broad. Most of the discordance could be accounted for after reassessing morphological characters. In these cases, the molecular data were invaluable in assisting taxonomic decision-making. The radiation of Nearctic species of Nephrocerus could not be diagnosed using cox1. The ability of cox1 to recover phylogenetic signal was also tested on Clistoabdominalis. Morphological data for Clistoabdominalis were combined with the molecular data set. The pipunculid phylogeny from molecular data closely resembles the published phylogeny based on morphology. Partitioned Bremer support is used to localize areas of conflict between the datasets.


2015 ◽  
Vol 46 (3) ◽  
pp. 269-290 ◽  
Author(s):  
Ian J. Kitching ◽  
C. Lorna Culverwell ◽  
Ralph E. Harbach

Lutzia Theobald was reduced to a subgenus of Culex in 1932 and was treated as such until it was restored to its original generic status in 2003, based mainly on modifications of the larvae for predation. Previous phylogenetic studies based on morphological and molecular data have provided conflicting support for the generic status of Lutzia: analyses of morphological data support the generic status whereas analyses based on DNA sequences do not. Our previous phylogenetic analyses of Culicini (based on 169 morphological characters and 86 species representing the four genera and 26 subgenera of Culicini, most informal group taxa of subgenus Culex and five outgroup species from other tribes) seemed to indicate a conflict between adult and larval morphological data. Hence, we conducted a series of comparative and data exclusion analyses to determine whether the alternative positions of Lutzia are due to conflicting signal or to a lack of strong signal. We found that separate and combined analyses of adult and larval data support different patterns of relationships between Lutzia and other Culicini. However, the majority of conflicting clades are poorly supported and once these are removed from consideration, most of the topological disparity disappears, along with much of the resolution, suggesting that morphology alone does not have sufficiently strong signal to resolve the position of Lutzia. We critically examine the results of other phylogenetic studies of culicinine relationships and conclude that no morphological or molecular data set analysed in any study conducted to date has adequate signal to place Lutzia unequivocally with regard to other taxa in Culicini. Phylogenetic relationships observed thus far suggest that Lutzia is placed within Culex but further data and extended taxon sampling are required to confirm its position relative to Culex.


2003 ◽  
Vol 34 (2) ◽  
pp. 199-219 ◽  
Author(s):  
Torbjørn Ekrem

AbstractA phylogenetic analysis of species potentially belonging to the Tanytarsus eminulus, gregarius, mendax and lugens species groups is performed using morphological characters from the adult male, pupa and larva. The results show that morphological characters do not support the postulated monophyly of the eminulus, gregarius, lugens and mendax group combined in unweighted parsimony analyses, and that a constraint based on unique synapomorphies and evidence from molecular data have to be used in order to produce cladograms with reasonable topologies. Four reasons for this are discussed: Few taxa, few characters, choice of secondary outgroup taxa and a high amount of homoplasy in the data set. A hierarchial analysis procedure is used to avoid the numerous question marks in the complete data matrix. In the preferred tree, the traditional species groups within Tanytarsus are kept, and one new species group, the mcmillani group, comprising only old Gondwanan species is erected. The results are compared to other recent studies on chironomid species relationships, and comments are given to the zoogeographical patterns of the species in the eminulus, gregarius, lugens, mcmillani and mendax species groups.


2011 ◽  
Vol 279 (1731) ◽  
pp. 1093-1099 ◽  
Author(s):  
Maria Heikkilä ◽  
Lauri Kaila ◽  
Marko Mutanen ◽  
Carlos Peña ◽  
Niklas Wahlberg

Although the taxonomy of the ca 18 000 species of butterflies and skippers is well known, the family-level relationships are still debated. Here, we present, to our knowledge, the most comprehensive phylogenetic analysis of the superfamilies Papilionoidea, Hesperioidea and Hedyloidea to date based on morphological and molecular data. We reconstructed their phylogenetic relationships using parsimony and Bayesian approaches. We estimated times and rates of diversification along lineages in order to reconstruct their evolutionary history. Our results suggest that the butterflies, as traditionally understood, are paraphyletic, with Papilionidae being the sister-group to Hesperioidea, Hedyloidea and all other butterflies. Hence, the families in the current three superfamilies should be placed in a single superfamily Papilionoidea. In addition, we find that Hedylidae is sister to Hesperiidae, and this novel relationship is supported by two morphological characters. The families diverged in the Early Cretaceous but diversified after the Cretaceous–Palaeogene event. The diversification of butterflies is characterized by a slow speciation rate in the lineage leading to Baronia brevicornis , a period of stasis by the skippers after divergence and a burst of diversification in the lineages leading to Nymphalidae, Riodinidae and Lycaenidae.


2010 ◽  
Vol 84 (3) ◽  
pp. 336-339 ◽  
Author(s):  
G. Marucci ◽  
G. La Rosa ◽  
E. Pozio

AbstractMolecular analyses such as polymerase chain reaction (PCR) and sequencing are very useful for taxon identification, especially when morphological characters useful for identifying taxa are lacking. However, the use of molecular tools can be the source of taxon misidentification if they are not correctly applied and the results are not critically evaluated and compared with the literature and GenBank data. We describe a case of misidentification of a taxon of the genus Trichinella due to sequencing mistakes, lack of reference material and selection of a single molecular marker. A Trichinella sp. isolate from an Iranian wild boar (Sus scrofa) was identified as belonging to the Nearctic species Trichinella murrelli, through the molecular analysis of the 5S rRNA intergenic spacer region. A successive molecular identification of the same isolate was performed by the International Trichinella Reference Centre in Rome, Italy, using the 5S rRNA intergenic spacer region, the LSU rDNA expansion segment five, and the internal transcribed spacers 1 and 2. According to these analyses, the Iranian isolate belonged to Trichinella britovi, a Palaearctic species already described in Iran.


Parasitology ◽  
2003 ◽  
Vol 126 (3) ◽  
pp. 203-224 ◽  
Author(s):  
A. E. LOCKYER ◽  
P. D. OLSON ◽  
P. ØSTERGAARD ◽  
D. ROLLINSON ◽  
D. A. JOHNSTON ◽  
...  

Schistosomes are digenean flukes, parasitic of birds, mammals and crocodiles. The family Schistosomatidae contains species of considerable medical and veterinary importance, which cause the disease schistosomiasis. Previous studies, both morphological and molecular, which have provided a good deal of information on the phylogenetics of this group, have been limited in the number of species investigated or the type or extent of molecular data used. This paper presents the most comprehensive phylogeny to date, based on the sequences of 3 genes, complete ribosomal small subunit rRNA and large ribosomal subunit rRNA, and mitochondrial cytochrome oxidase 1, sequenced from 30 taxa including at least 1 representative from 10 of the 13 known genera of the Schistosomatidae and 17 of the 20 recognized Schistosoma species. The phylogeny is examined using morphological characters, intermediate and definitive host associations and biogeography. Theories as to the origins and spread of Schistosoma are also explored. The principal findings are that Ornithobilharzia and Austrobilharzia form a sister group to the Schistosoma; mammalian schistosomes appear paraphyletic and 2 Trichobilharzia species, T. ocellata and T. szidati, seem to be synonymous. The position of Orientobilharzia within the Schistosoma is confirmed, as is an Asian origin for the Schistosoma, followed by subsequent dispersal through India and Africa.


2005 ◽  
Vol 272 (1572) ◽  
pp. 1577-1586 ◽  
Author(s):  
Niklas Wahlberg ◽  
Michael F Braby ◽  
Andrew V.Z Brower ◽  
Rienk de Jong ◽  
Ming-Min Lee ◽  
...  

Phylogenetic relationships among major clades of butterflies and skippers have long been controversial, with no general consensus even today. Such lack of resolution is a substantial impediment to using the otherwise well studied butterflies as a model group in biology. Here we report the results of a combined analysis of DNA sequences from three genes and a morphological data matrix for 57 taxa (3258 characters, 1290 parsimony informative) representing all major lineages from the three putative butterfly super-families (Hedyloidea, Hesperioidea and Papilionoidea), plus out-groups representing other ditrysian Lepidoptera families. Recently, the utility of morphological data as a source of phylogenetic evidence has been debated. We present the first well supported phylogenetic hypothesis for the butterflies and skippers based on a total-evidence analysis of both traditional morphological characters and new molecular characters from three gene regions ( COI , EF-1α and wingless ). All four data partitions show substantial hidden support for the deeper nodes, which emerges only in a combined analysis in which the addition of morphological data plays a crucial role. With the exception of Nymphalidae, the traditionally recognized families are found to be strongly supported monophyletic clades with the following relationships: (Hesperiidae+(Papilionidae+(Pieridae+(Nymphalidae+(Lycaenidae+Riodinidae))))). Nymphalidae is recovered as a monophyletic clade but this clade does not have strong support. Lycaenidae and Riodinidae are sister groups with strong support and we suggest that the latter be given family rank. The position of Pieridae as the sister taxon to nymphalids, lycaenids and riodinids is supported by morphology and the EF-1α data but conflicted by the COI and wingless data. Hedylidae are more likely to be related to butterflies and skippers than geometrid moths and appear to be the sister group to Papilionoidea+Hesperioidea.


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