A molecular phylogeny of the subfamily Arundinoideae (Poaceae) based on sequences of rDNA

1998 ◽  
Vol 11 (1) ◽  
pp. 41 ◽  
Author(s):  
C. Hsiao ◽  
S. W. L. Jacobs ◽  
N. P. Barker ◽  
N. J. Chatterton

Phylogenetic relationships of the whole Poaceae family inferred from the sequence data of rDNA (ITS) support the hypothesis that the arundinoids are monophyletic, not polyphyletic as previously proposed. The ITS sequence phylogeny of 42 arundinoid species demonstrates an early divergence of the Aristideae and three major groupings, corresponding loosely to the tribes Aristideae, Arundineae and Danthonieae. The Arundineae are resolved into two paraphyletic clades. In one clade, Arundo, Monachather, and Dregeochloa are the sister group to Amphipogon and Diplopogon. In the other clade, Phragmites, Molinia, Gynerium, Thysanolaena, Spartochloa, and Cyperochloa are the sister group to Eriachne and Micraira. Arundo is not closely related to Phragmites. The Danthonieae clade, including taxa from Africa, Australia, New Guinea, New Zealand, the South American Cortaderia, and the North American Danthonia, appears to be monophyletic. However, the genus Merxmuellera is polyphyletic.

2019 ◽  
Vol 44 (4) ◽  
pp. 930-942
Author(s):  
Geraldine A. Allen ◽  
Luc Brouillet ◽  
John C. Semple ◽  
Heidi J. Guest ◽  
Robert Underhill

Abstract—Doellingeria and Eucephalus form the earliest-diverging clade of the North American Astereae lineage. Phylogenetic analyses of both nuclear and plastid sequence data show that the Doellingeria-Eucephalus clade consists of two main subclades that differ from current circumscriptions of the two genera. Doellingeria is the sister group to E. elegans, and the Doellingeria + E. elegans subclade in turn is sister to the subclade containing all remaining species of Eucephalus. In the plastid phylogeny, the two subclades are deeply divergent, a pattern that is consistent with an ancient hybridization event involving ancestral species of the Doellingeria-Eucephalus clade and an ancestral taxon of a related North American or South American group. Divergence of the two Doellingeria-Eucephalus subclades may have occurred in association with northward migration from South American ancestors. We combine these two genera under the older of the two names, Doellingeria, and propose 12 new combinations (10 species and two varieties) for all species of Eucephalus.


Botany ◽  
2008 ◽  
Vol 86 (9) ◽  
pp. 1039-1064 ◽  
Author(s):  
Stephen R. Downie ◽  
Deborah S. Katz-Downie ◽  
Feng-Jie Sun ◽  
Chang-Shook Lee

Intergeneric phylogenetic relationships within Apiaceae tribe Oenantheae were investigated using sequence data from the chloroplast DNA psbI–5′trnK(UUU) and nuclear ribosomal DNA internal transcribed spacer regions. One hundred and thirty-one accessions were examined, representing all 17 genera of the tribe and approximately one-half of its species. The cpDNA region includes four intergenic spacers and the rps16 intron and these noncoding loci were analyzed separately to assess their relative utility for resolving relationships. Separate maximum parsimony analyses of the entire psbI–5′trnK(UUU) and ITS regions, each with and without scored indels, yielded concordant trees. Phylogenies derived from maximum parsimony, Bayesian, or maximum likelihood analyses of combined chloroplast and nuclear DNA sequences for 82 accessions were highly resolved, well supported, and consistent. Among the five noncoding loci examined, the trnQ(UUG)–5′rps16 and 3′rps16–5′trnK(UUU) intergenic spacers are the most variable, with the latter contributing the greatest total number of parsimony informative characters relative to its size. The North American genera Atrema , Cynosciadium , Daucosma , Limnosciadium , Neogoezia , Oxypolis , Ptilimnium , and Trepocarpus ally with the western hemispheric and Australasian genus Lilaeopsis in a strongly supported North American Endemics clade that is a sister group to a clade composed primarily of Old World taxa ( Berula sensu lato, Cryptotaenia , Helosciadium , and Sium ). Oxypolis and Ptilimnium are not monophyletic, with the rachis-leaved members of each comprising a clade separate from their compound-leaved congeners. Dispersal-vicariance analysis suggests that the ancestors of the North American Endemics clade probably originated in Canada and the USA or in a broader ancestral area including Mexico and South America.


2006 ◽  
Vol 84 (3) ◽  
pp. 453-468 ◽  
Author(s):  
Chang-Shook Lee ◽  
Stephen R. Downie

The genus Cicuta (Apiaceae tribe Oenantheae Dumort.) is the most virulently poisonous group of flowering plants native to the north temperate zone. A recent treatment recognized four species ( C. bulbifera L., C. douglasii (DC.) J.M. Coult. & Rose, C. maculata L., and C. virosa L.), with C. maculata divided into four varieties. We present results of phylogenetic analyses of the nuclear ribosomal DNA (rDNA) internal transcribed spacer (ITS) locus and the region bounded by the chloroplast genes psbI and trnK 5′ exon to determine taxonomic limits and relationships among these taxa, and to assess the taxonomic status of C. douglasii, a polyploid thought to be derived from C. maculata and C. virosa. Cicuta bulbifera and C. virosa are each resolved as monophyletic, the latter is a sister group to all other species. Discordance between the ITS- and plastid-derived phylogenies and lack of resolution in the ITS trees preclude unequivocal hypotheses of relationship; all trees do suggest, however, that the allotetraploid C. douglasii is polyphyletic and possibly polytopic, with all examined accessions but one nested within C. maculata. This single outstanding accession is from California and, pending further study, might warrant recognition as a distinct species. The diploid C. bulbifera may also be of hybrid origin, as revealed by significant discordance between data sets. Within C. maculata, only the western North American var. angustifolia Hook. is resolved in the ITS trees. In the cpDNA trees, C. maculata var. angustifolia comprises a strongly supported clade with C. maculata var. bolanderi (S. Watson) G.A. Mulligan and C. douglasii, both of primarily western North American distribution. The eastern North American taxa, C. maculata vars. maculata and victorinii (Fernald) B. Boivin, also comprise a clade, sister group to C. bulbifera.


1968 ◽  
Vol 25 (5) ◽  
pp. 877-901 ◽  
Author(s):  
Wilfred Templeman

Three specimens of Halargyreus johnsonii taken on the southwestern and southeastern slopes of the Grand Bank in 1959 and 1964 are apparently the first records of this species and genus from the western Atlantic. These specimens are compared with the holotypes of H. johnsonii Günther and of H. brevipes Vaillant and with the syntypes of H. affinis Collett and also with specimens identified as H. affinis from the north-central and northeast Atlantic and with specimens of H. johnsonii from Madeira and New Zealand. These three nominal species are also compared. Is it concluded that for the present all North Atlantic specimens may be referred to H. johnsonii and that the other two species names should be considered as junior synonyms of H. johnsonii.The New Zealand specimens of Halargyreus, described by Günther (1887, Challenger Rept., 22(Zoology), p. 1–268) as H. johnsonii, have higher numbers for some meristic characters than Atlantic specimens of H. johnsonii but these differences are not too great to be possibly due to environmental differences. Pending the study of additional specimens in better condition, these New Zealand specimens are tentatively allowed to remain as H. johnsonii.


Zootaxa ◽  
2009 ◽  
Vol 2021 (1) ◽  
pp. 57-65 ◽  
Author(s):  
JOHN S. BUCKERIDGE

A new deep-sea stalked barnacle, Ashinkailepas kermadecensis sp. nov. has been recovered from a cold-water seep at depths of 1165 metres in the vicinity of the Kermadec Ridge to the northeast of the North Island, New Zealand. There are now two species of Ashinkailepas—the other, Ashinkailepas seepiophila Yamaguchi, Newman & Hashimoto, 2004, occurs in deep, cold seeps off central Japan. As there are two species within Ashinkailepas, formal diagnoses are provided for both taxa.


2021 ◽  
Author(s):  
Gonzalo Giribet ◽  
Kate Sheridan ◽  
Caitlin M. Baker ◽  
Christina J. Painting ◽  
Gregory I. Holwell ◽  
...  

The Opiliones family Neopilionidae is restricted to the terranes of the former temperate Gondwana: South America, Africa, Australia, New Caledonia and New Zealand. Despite decades of morphological study of this unique fauna, it has been difficult reconciling the classic species of the group (some described over a century ago) with recent cladistic morphological work and previous molecular work. Here we attempted to investigate the pattern and timing of diversification of Neopilionidae by sampling across the distribution range of the family and sequencing three markers commonly used in Sanger-based approaches (18S rRNA, 28S rRNA and cytochrome-c oxidase subunit I). We recovered a well-supported and stable clade including Ballarra (an Australian ballarrine) and the Enantiobuninae from South America, Australia, New Caledonia and New Zealand, but excluding Vibone (a ballarrine from South Africa). We further found a division between West and East Gondwana, with the South American Thrasychirus/Thrasychiroides always being sister group to an Australian–Zealandian (i.e. Australia + New Zealand + New Caledonia) clade. Resolution of the Australian–Zealandian taxa was analysis-dependent, but some analyses found Martensopsalis, from New Caledonia, as the sister group to an Australian–New Zealand clade. Likewise, the species from New Zealand formed a clade in some analyses, but Mangatangi often came out as a separate lineage from the remaining species. However, the Australian taxa never constituted a monophyletic group, with Ballarra always segregating from the remaining Australian species, which in turn constituted 1–3 clades, depending on the analysis. Our results identify several generic inconsistencies, including the possibility of Thrasychiroides nested within Thrasychirus, Forsteropsalis being paraphyletic with respect to Pantopsalis, and multiple lineages of Megalopsalis in Australia. In addition, the New Zealand Megalopsalis need generic reassignment: Megalopsalis triascuta will require its own genus and M. turneri is here transferred to Forsteropsalis, as Forsteropsalis turneri (Marples, 1944), comb. nov.


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