The genealogy of geebungs: phylogenetic analysis of Persoonia (Proteaceae) and related genera in subfamily Persoonioideae

2018 ◽  
Vol 31 (2) ◽  
pp. 166
Author(s):  
Gareth D. Holmes ◽  
Peter H. Weston ◽  
Daniel J. Murphy ◽  
Carolyn Connelly ◽  
David J. Cantrill

Proteaceae subfamily Persoonioideae, as presently circumscribed, consists of the monogeneric tribe Placospermeae (Placospermum) and the tribe Persoonieae. The latter comprises the diverse genus Persoonia and monospecific genera found in New Zealand (Toronia), New Caledonia (Garnieria) and south-western Western Australia (Acidonia). Persoonia has 101 species distributed across Australia and has been classified into 11 informal groups. Using data derived from plastid DNA (trnL–trnF region), nuclear rDNA (ITS) and morphological characters, we constructed a phylogeny of Persoonioideae and compared the results to the existing classification. Bayesian and parsimony analyses indicated that Persoonia, as currently defined, is non-monophyletic. The molecular data and combined molecular and morphological data place Toronia in a moderately well supported clade with the monophyletic Rufiflora group of Persoonia from Western Australia. This clade is sister to Acidonia, Garnieria and the remaining Persoonia species. Of the other informal groups in Persoonia, the Teretifolia, Quinquenervis, Laurina, Arborea, Graminea and Chapmaniana groups are supported as monophyletic. The Lanceolata group can be re-circumscribed to be monophyletic by the addition of P. elliptica R.Br. (Longifolia group) and the Dillwynioides group. Relationships within this large, geographically widespread clade are largely unresolved and low DNA-sequence variation within it suggests a recent radiation followed by isolation in south-western and eastern Australia. All endemic Tasmanian Persoonia (Gunnii group taxa) are unresolved at the second-most basal node of the Persoonieae. Our results suggest that the Rufiflora group should be treated as a new genus and that the infrageneric taxonomy of Persoonia requires minor amendment.

2006 ◽  
Vol 37 (3) ◽  
pp. 241-256 ◽  
Author(s):  
Donald Colgan ◽  
Gregory Edgecombe ◽  
Deirdre Sharkey

AbstractThe lithobiomorph centipede Henicops is widely distributed in Australia and New Zealand, with five described species, as well as two species in New Caledonia and Lord Howe Island. Parsimony, maximum likelihood and Bayesian analyses of ca. 800 aligned bases of sequence data from 16S rRNA and 28S rRNA were conducted on a dataset including multiple individuals of Henicops species from populations sampled from different parts of species' geographic ranges, together with the allied henicopines Lamyctes and Easonobius. Morphological characters are included in parsimony analyses. Molecular and combined datasets unite species from eastern Australia and New Zealand to the exclusion of species from Western Australia, New Caledonia and Lord Howe Island. The molecular data favour these two geographic groupings as clades, whereas inclusion of morphology resolves New Caledonia, Lord Howe Island, southwest Western Australia and Queensland as successive sisters to southeastern Australia and New Zealand. The basal position of the Lord Howe Island species in the phylogeny favours a diversification of Australasian Henicops since the late Miocene unless the Lord Howe species originated in a biota that pre-dates the island. The molecular and combined data resolve the widespread morphospecies H. maculatus as paraphyletic, with its populations contributing to the geographic groupings New South Wales + New Zealand and Tasmania + Victoria.


Telopea ◽  
2021 ◽  
Vol 24 ◽  
pp. 61-169
Author(s):  
Russell Barrett ◽  

The Tricostularia Nees ex Lehm. group of genera is reviewed and formally recognised as Cyperaceae tribe Schoeneae subtribe Tricostulariinae R.L.Barrett, K.L.Wilson & J.J.Bruhl. Molecular data from plastid rbcL and trnL–F and nuclear ITS and ETS regions are combined with a novel assessment of morphological characters to support our new classification. Six genera are included: a new genus, Ammothryon R.L.Barrett, K.L.Wilson & J.J.Bruhl, and the named genera Chaetospora R.Br., Morelotia Gaudich., Tetraria P.Beauv., Tricostularia, and Xyroschoenus Larridon. Ammothryon, Chaetospora and Tricostularia are all endemic to southern Australia. Morelotia has one species each in Hawaii, French Polynesia and New Zealand, and three species in southwest Western Australia. Tetraria has a disjunct distribution in Southern Africa, Borneo, New Guinea and New Caledonia. Xyroschoenus is endemic to the Seychelles. Tetrariopsis C.B.Clarke (based on Tetrariopsis octandra (Nees) C.B.Clarke) is included under an expanded concept of Morelotia, which also includes Tetraria australiensis C.B.Clarke and Tetraria microcarpa S.T.Blake from south-west Western Australia. Tricostularia bennettiana R.L.Barrett & K.L.Wilson, Tricostularia davisii R.L.Barrett & K.L.Wilson, Tricostularia lepschii R.L.Barrett & K.L.Wilson, Tricostularia newbeyi R.L.Barrett & K.L.Wilson, and Tricostularia sandifordiana R.L.Barrett & K.L.Wilson are described as new species from south-west Western Australia. The following new combinations are made: Ammothryon grandiflorum (Nees ex Lehm.) R.L.Barrett, K.L.Wilson & J.J.Bruhl, Morelotia australiensis (C.B.Clarke) R.L.Barrett & K.L.Wilson, Morelotia microcarpa (S.T.Blake) R.L.Barrett & K.L.Wilson, Morelotia octandra (Nees) R.L.Barrett & J.J.Bruhl and Tricostularia drummondii (Steud.) R.L.Barrett & K.L.Wilson. Tricostularia drummondii is reinstated from synonymy (formerly Discopodium drummondii Steud.), having previously been confused with T. exsul (C.B.Clarke) K.L.Wilson & R.L.Barrett. Lectotypes are selected for Chaetospora flexuosa var. gracilis Boeckeler, Discopodium drummondii Steud., Elynanthus grandiflorus Nees ex Lehm., Lampocarya affinis Brongn., Lepidosperma exsul C.B.Clarke, Morelotia gahniiformis Gaudich. var. minor A.Rich., Tetraria australiensis C.B.Clarke, Tetraria capillacea var. intercedens Kük., Tricostularia compressa Nees ex Lehm. and Tricostularia neesii Lehm.


2021 ◽  
Vol 307 (2) ◽  
Author(s):  
Pau Carnicero ◽  
Núria Garcia-Jacas ◽  
Llorenç Sáez ◽  
Theophanis Constantinidis ◽  
Mercè Galbany-Casals

AbstractThe eastern Mediterranean basin hosts a remarkably high plant diversity. Historical connections between currently isolated areas across the Aegean region and long-distance dispersal events have been invoked to explain current distribution patterns of species. According to most recent treatments, at least two Cymbalaria species occur in this area, Cymbalaria microcalyx and C. longipes. The former comprises several intraspecific taxa, treated at different ranks by different authors based on morphological data, evidencing the need of a taxonomic revision. Additionally, some populations of C. microcalyx show exclusive morphological characters that do not match any described taxon. Here, we aim to shed light on the systematics of eastern Mediterranean Cymbalaria and to propose a classification informed by various sources of evidence. We performed molecular phylogenetic analyses using ITS, 3’ETS, ndhF and rpl32-trnL sequences and estimated the ploidy level of some taxa performing relative genome size measures. Molecular data combined with morphology support the division of traditionally delimited C. microcalyx into C. acutiloba, C. microcalyx and C. minor, corresponding to well-delimited nrDNA lineages. Furthermore, we propose to combine C. microcalyx subsp. paradoxa at the species level. A group of specimens previously thought to belong to Cymbalaria microcalyx constitute a well-defined phylogenetic and morphological entity and are described here as a new species, Cymbalaria spetae. Cymbalaria longipes is non-monophyletic, but characterized by being glabrous and diploid, unlike other eastern species. The nrDNA data suggest at least two dispersals from the mainland to the Aegean Islands, potentially facilitated by marine regressions.


Zootaxa ◽  
2004 ◽  
Vol 680 (1) ◽  
pp. 1 ◽  
Author(s):  
ARNE NYGREN

Autolytinae is revised based on available types, and newly collected specimens. Out of 170 nominal species, 18 are considered as incertae sedis, 43 are regarded as junior synonyms, and 25 are referred to as nomina dubia. The relationships of Autolytinae is assessed from 51 morphological characters and 211 states for 76 ingroup-taxa, and 460 molecular characters from mitochondrial 16S rDNA and nuclear 18S rDNA for 31 ingroup-taxa; outgroups include 12 non-autolytine syllid polychaetes. Two analyses are provided, one including morphological data only, and one with combined morphological and molecular data sets. The resulting strict consensus tree from the combined data is chosen for a reclassification. Three main clades are identified: Procerini trib. n., Autolytini Grube, 1850, and Epigamia gen. n. Proceraea Ehlers, 1864 and Myrianida Milne Edwards, 1845 are referred to as nomen protectum, while Scolopendra Slabber, 1781, Podonereis Blainville, 1818, Amytis Savigny, 1822, Polynice Savigny, 1822, and Nereisyllis Blainville, 1828 are considered


Zootaxa ◽  
2010 ◽  
Vol 2505 (1) ◽  
pp. 1 ◽  
Author(s):  
JOHN E. McCOSKER

The 19 Indo-Pacific species of the snake-eel genus Ophichthus (family Ophichthidae, subfamily Ophichthinae) that live at or below 200 m are reviewed. Included are: Ophichthus aphotistos, O. brachynotopterus, O. echeloides, O. exourus, O. genie, O. kunaloa, O. megalops, O. mystacinus, O. serpentinus, O. urolophus, and nine new species which are described: O. alleni from 115–200 m off eastern Australia; O. aniptocheilos from 391–421 m off Tonga; O. congroides from 300 m off the Tuamotu Islands; O. hirritus from 600 m off the Seychelle Islands; O. humanni from 254–300 m off Vanuatu; O. ishiyamorum from 258–400 m off the Gulf of Aden, Somalia; O. lentiginosus from 400 m off Vanuatu and New Caledonia; O. microstictus from 362–450 m off Tonga, Fiji, and possibly New Caledonia; and O. tomioi from 300– 423 m off the Philippines, Marquesas, Fiji, and the Seychelle Islands. The range and depth distributions of the following are expanded to include: O. brachynotopterus to New Caledonia and Vanuatu between 541–580 m; O. mystacinus to Tonga, Fiji, and the Philippines between 371–824 m; and O. urolophus to Western Australia and Indonesia between 40– 420 m. An identification key is provided. Characteristics and the behavior of species of the subgenus Coecilophis, to which all treated species except O. aphotistos belong, is discussed. Ophichthys madagascariensis Fourmanoir (1961) is proposed to be a junior synonym of Pisodonophis cancrivorus (Richardson 1848).


2013 ◽  
Vol 26 (6) ◽  
pp. 408 ◽  
Author(s):  
Matt A. M. Renner ◽  
Nicolas Devos ◽  
Elizabeth A. Brown ◽  
Matt J. von Konrat

The current paper presents molecular data from three chloroplast markers (atpB–rbcL spacer, trnG G2 intron, trnL–trnF intron and spacer); morphological data, and geographic data to support the recognition of nine species belonging to Radula subg. Odontoradula in Australasia. R. ocellata, the subgeneric type from the Wet Tropics bioregion, is maintained as distinct from its sister species, R. pulchella, from south-eastern Australian rainforests; both species are Australian endemics. Reinstatement of R. allisonii from synonymy, under R. retroflexa, is supported by molecular data and morphological characters, including the absence of triradiate trigones on leaf-lobe cell walls, the apex of lobules on primary shoots not being turned outwards, the oblong-elliptic female bracts, and the perianths having a pronounced wing. Reinstatement of R. weymouthiana, from synonymy under R. retroflexa, is also supported by molecular data and morphological characters, including the presence of a single low dome-shaped papilla over each leaf-lobe cell, and the large imbricate lobules on primary shoots. R. weymouthiana occurs in Tasmania and New Zealand, whereas R. allisonii is a New Zealand endemic. Australian R. retroflexa exhibits differentiation into epiphytic and rheophytic morphs, interpreted as ecotypes. Australian individuals, comprising both epiphytic and rheophytic morphs, are monophyletic and nested within a clade containing individuals from other regions. R. novae-hollandiae is newly reported for the New Zealand Botanical Region, from Raoul Island in the Kermadecs. R. novae-hollandiae exhibits decoupling of morphological and molecular divergence, with Australian individuals forming two clades reflecting geography (a Wet Tropics bioregion clade and a south-eastern Rainforest clade). These clades exhibit equivalent levels of molecular divergence, as observed in R. pulchella and R. ocellata, but no morphological differences. Similar levels of molecular divergence were observed in trans-Tasman populations of R. tasmanica. The New Zealand endemic, R. plicata, is excluded from the Australian flora, and R. cuspidata replaces R. dentifolia for the New Zealand endemic species formerly known by both names.


1979 ◽  
Vol 30 (3) ◽  
pp. 375 ◽  
Author(s):  
AJ Hadfield ◽  
V Ivantsoff ◽  
PG Johnson

Electrophoretic and morphological comparisons were made between 14 populations representing the major part of the known range of the nominal fish species, Pseudomugil signifer Kner and Pseudomugil signatus (Gunther), described from the fresh and brackish waters of eastern Australia. Analysis by principal components was used to assess the morphological data. .Clinal variation revealed in 10 morphological characters and at two enzyme loci was found to bridge most of the previously described differences between species. The type material of P. signatus afinis from the Low Isles, Queensland, was re-examined and did not appear to differ morphologically from the coastal species. It is therefore suggested that the populations studied represent a single species Pseudomugil signifer Kner.


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.


2016 ◽  
Vol 85 (4) ◽  
pp. 387-422 ◽  
Author(s):  
Roberto Arrigoni ◽  
Francesca Benzoni ◽  
Danwei Huang ◽  
Hironobu Fukami ◽  
Chaolun Allen Chen ◽  
...  

The scleractinian family Lobophylliidae is undergoing a major taxonomic revision thanks to the combination of molecular and morphological data. In this study, we investigate the evolutionary relationships and the macro- and micromorphology of six nominal coral species belonging to two of the nine molecular clades of the Lobophylliidae, clades A and B, and of Symphyllia wilsoni, a lobophylliid species analyzed from a molecular point of view for the first time. Sequence data from mitochondrial DNA (COI and the intergenic spacer between COI and l-rRNA), and nuclear DNA (histone H3 and ITS region) are used to generate robust molecular phylogenies and a median-joining haplotype network. Molecular results are strongly in agreement with detailed observations of gross- and fine-scale morphology of skeletons, leading to the formal revision of the genera Micromussa and Homophyllia and the description of two newly discovered zooxanthellate shallow-water species, Micromussa pacifica sp. nov. Benzoni & Arrigoni and Micromussa indiana sp. nov. Benzoni & Arrigoni, and a new genus, Australophyllia gen. nov. Benzoni & Arrigoni. In particular, Acanthastrea lordhowensis and Montastraea multipunctata are moved into Micromussa, A. hillae is synonymized with A. bowerbanki and is transferred to Homophyllia, and a revised diagnosis for both genera is provided. Micromussa pacifica sp. nov. is described from the Gambier Islands with its distribution spanning New Caledonia and eastern Australia. Despite a superficial resemblance with Homophyllia australis, it has distinctive macroand micromorphological septal features. Micromussa indiana sp. nov., previously identified as M. amakusensis, is here described from the Gulf of Aden and the southern Red Sea as a distinct species that is genetically separated from M. amakusensis and is morphologically distinct from the latter due to its smaller corallite size and lower number of septa. Finally, molecular trees show that S. wilsoni is closely related, but molecularly separated from clades A and B, and, also based on a unique combination of corallite and sub-corallite characters, the species is moved into Australophyllia gen. nov. These findings confirm the need for using both genetic and morphological datasets for the ongoing taxonomic revision of scleractinian corals.


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.


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