Internal phylogeny of the Chilopoda (Myriapoda, Arthropoda) using complete 18S rDNA and partial 28S rDNA sequences

The internal phylogeny of the ‘myriapod’ class Chilopoda is evaluated for 12 species belonging to the five extant centipede orders, using 18S rDNA complete gene sequence and 28S rDNA partial gene sequence data. Equally and differentially weighted parsimony, neighbour–joining and maximum–likelihood were used for phylogenetic reconstruction, and bootstrapping and branch support analyses were performed to evaluate tree topology stability. The results show that the Chilopoda constitute a monophyletic group that is divided into two lines, Notostigmophora (= Scutigeromorpha) and Pleurostigmophora, as found in previous morphological analyses. The Notostigmophora are markedly modified for their epigenic mode of life. The first offshoot of the Pleurostigmophora are the Lithobiomorpha, followed by the Craterostigmomorpha and by the Epimorpha s. str. (= Scolopendromorpha + Geophilomorpha), although strong support for the monophyly of the Epimorpha s. lat. (= Craterostigmomorpha + Epimorpha s. str.) is only found in the differentially weighted parsimony analysis.

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Systematic revision, cladistics and biogeography of the genus Neogutierrezia Martínez (Coleoptera:Scarabaeidae) and its phylogenetic placement in Rutelinae based on structural alignment of 28S rDNA sequences

Invertebrate Systematics ◽

10.1071/is09035 ◽

2010 ◽

Vol 24 (1) ◽

pp. 81 ◽

Cited By ~ 8

Author(s):

Federico C. Ocampo ◽

Eider Ruiz-Manzanos ◽

Adriana E. Marvaldi

Keyword(s):

Structural Alignment ◽

Phylogenetic Reconstruction ◽

Cladistic Analysis ◽

28S Rdna ◽

Structure Alignment ◽

28S Rrna ◽

Systematic Revision ◽

Rdna Sequences ◽

Molecular Phylogenetic ◽

28S Rdna Sequences

The Argentinean endemic genus Neogutierrezia Martínez, 1953 (Scarabaeidae : Rutelinae) is revised and seven new species are described: N. bicolor Ocampo & Ruiz-Manzanos, sp. nov., N. chelii Ocampo & Ruiz-Manzanos, sp. nov., N. galileoi Ocampo & Ruiz-Manzanos, sp. nov., N. lagosae Ocampo & Ruiz-Manzanos, sp. nov., N. payuniensis Ocampo & Ruiz-Manzanos, sp. nov., N. scutata Ocampo & Ruiz-Manzanos, sp. nov. and N. variabilis Ocampo & Ruiz-Manzanos, sp. nov. Species status is proposed for N. affinis Martínez stat. nov., which was formerly considered as subspecies of N. mirabilis Martínez. The genus Neogutierrezia now includes 10 species distributed in the Monte biogeographic province in Argentina. In order to clarify the systematic placement of the genus Neogutierrezia, a molecular phylogenetic analysis was performed using structurally aligned 28S rDNA sequences (expansion segments D2 and D3) from 23 taxa in Scarabaeoidea, including two representative species of Neogutierrezia. This is the first report of an annotated secondary structure alignment of the D2 and D3 segments of 28S rRNA that spans a wide sample of scarabaeoids, providing a useful homology template for further phylogenetic reconstruction in these and closely related beetles. Results of the molecular parsimony analysis strongly indicate that the genus is closely related to members of the Rutelinae (Scarabaeidae), and thus Neogutierrezia Martínez is transferred from Melolonthinae: Pachydemini to Rutelinae, new placement. A morphological cladistic analysis of the genus was also undertaken, including all the 10 known species in the genus plus two outgroup taxa in Rutelinae, and based on 53 adult characters. The most-parsimonious cladogram provides evidence for the monophyly of the genus, which shows three main clades, distributed in Central Monte and Southern Monte. The adult morphology of the 10 species is described and a key is provided, along with illustrations of the diagnostic characters. The biogeography of species in the genus is discussed.

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Description of Calcaridorylaimus heynsi n. sp. (Nematoda: Dorylaimidae) from Potchefstroom, South Africa

Nematology ◽

10.1163/15685411-00003346 ◽

2020 ◽

Vol 22 (8) ◽

pp. 855-865

Author(s):

Antoinette Swart ◽

Hendrika Fourie ◽

Louwrens R. Tiedt ◽

Milad Rashidifard

Keyword(s):

South Africa ◽

Phylogenetic Analysis ◽

New Species ◽

18S Rdna ◽

Molecular Techniques ◽

28S Rdna ◽

Median Line ◽

Rdna Sequences ◽

28S Rdna Sequences ◽

Short Body

Summary Calcaridorylaimus heynsi n. sp. is the second species of the genus to be described by both morphological and molecular techniques. Morphologically, it can be distinguished from all known species of Calcaridorylaimus by a combination of the following characters: presence of advulval ornamentations, short body (0.90-1.33 mm), slightly anteriorly positioned vulva (V = 47.6 (45.8-49.8)), short odontostyle in females and males (13.1 (11.5-14.5) μm and 13.5 (12.0-18.0) μm, respectively), number of supplements (2 + 9-11), short spicules when measured along the median line (40.4 (38-42) μm) and pore-like vulval opening. It is closest to C. sirgeli, especially in the presence of advulval ornamentations and the pore-like vulva. Phylogenetic analysis based on partial D2-D3 segment of 28S rDNA sequences showed that C. heynsi n. sp. is in a well-supported sister relation with Mesodorylaimus sp. in a clade with C. cignatus and Mesodorylaimus spp. In the Bayesian tree, using partial sequences 18S rDNA, M. japonicus was the closest taxon to the new species.

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Phylogenetic Positions of the Bothitrematidae and Neocalceostomatidae (Monopisthocotylean Monogeneans) Inferred from 28S rDNA Sequences

Comparative Parasitology ◽

10.1654/1525-2647(2002)069[0020:ppotba]2.0.co;2 ◽

2002 ◽

Vol 69 (1) ◽

pp. 20-25 ◽

Cited By ~ 11

Author(s):

Jean-Lou Justine ◽

Richard Jovelin ◽

Lassâd Neifar ◽

Isabelle Mollaret ◽

L. H Susan Lim ◽

...

Keyword(s):

28S Rdna ◽

Rdna Sequences ◽

28S Rdna Sequences

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Generic classification of some more hyphomycetes with solitary conidia borne on phialides

Canadian Journal of Botany ◽

10.1139/b98-104 ◽

1998 ◽

Vol 76 (9) ◽

pp. 1570-1583 ◽

Cited By ~ 7

Author(s):

W Gams ◽

K O'Donnell ◽

H -J Schroers ◽

M Christensen

Keyword(s):

New Species ◽

Phylogenetic Analyses ◽

Large Subunit ◽

Elongation Factor ◽

28S Rdna ◽

New Combination ◽

Rdna Sequences ◽

28S Rdna Sequences ◽

Three New Species ◽

Morphological Species

Unlike most phialide-producing fungi that liberate a multiplicity of conidia from each conidiogenous cell, only single conidia are formed on phialide-like conidiogenous cells in Aphanocladium, Verticimonosporium, and some species of Sibirina. A group of isolates obtained from soil of native Artemisia tridentata (sagebrush) grassland in Wyoming and from desert soil in Iraq is compared with these genera and classified as a fourth genus, Stanjemonium, honouring Stanley J. Hughes. Phylogenetic analyses of partial nuclear small- (18S) and large-subunit (28S) rDNA sequences indicate that Stanjemonium spp. form a monophyletic group with Emericellopsis. Sequences from the nuclear 18S and 28S rDNA were too conserved to resolve morphological species of Stanjemonium; however, phylogenetic analysis of b-tubulin and translation elongation factor 1a gene exons and introns resolved all species distinguished morphologically. Numerous conidiogenous cells or denticles are scattered along the cells of aerial hyphae in Aphanocladium and Stanjemonium spp., very rapidly collapsing into denticles in the former, somewhat more persistent and leaving broad scars in the latter. In Cladobotryum-Sibirina and Verticimonosporium spp., conidiogenous cells are discrete in terminal and intercalary whorls; phialides of the latter taxon are particularly swollen. The taxonomy of Aphanocladium is not yet resolved. Two species are recognized in Verticimonosporium. Three new species of Stanjemonium are described, and one new combination from Aphanocladium is proposed, along with one new species of Cladobotryum.Key words: Aphanocladium, Cladobotryum, conidiogenesis, hyphomycetes, molecular phylogeny, phialide, Stanjemonium, systematics, Verticimonosporium.

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Macrostomum shenda and M. spiriger, two new brackish-water species of Macrostomum (Platyhelminthes: Macrostomorpha) from China

Zootaxa ◽

10.11646/zootaxa.4603.1.5 ◽

2019 ◽

Vol 4603 (1) ◽

pp. 105

Author(s):

FAN XIN ◽

SI-YU ZHANG ◽

YONG-SHI SHI ◽

LEI WANG ◽

YU ZHANG ◽

...

Keyword(s):

Brackish Water ◽

Phylogenetic Analyses ◽

28S Rdna ◽

Body Region ◽

Rdna Sequences ◽

Molecular Phylogenetic ◽

28S Rdna Sequences ◽

Pore Opening ◽

Brackish Water Species ◽

Water Species

In this study, two new brackish-water species of Macrostomum (M. shenda n. sp. and M. spiriger n. sp.) collected from Shenzhen, China, were described based on morphological, histological, and molecular phylogenetic analyses. Macrostomum shenda n. sp. differs from its congeners in the oblique and non-thickening distal opening of its narrow funnel-shaped stylet. In addition, its sperm have neither bristles nor brush, and are surrounded by an undulating membrane in the mid-body region. In M. spiriger n. sp., the stylet is spirally twisted. Its reproductive apparatus has a seminal bursal pore opening exteriorly. Results of the 18S and 28S rDNA phylogenetic analyses also support the establishments of these two new species. Moreover, the 18S and 28S rDNA sequences of some species within Macrostomum in previous studies have been revised to avoid ambiguity, while Macrostomum dongyuanensis Wang & Sun, 2015 was re-identified as a new record of M. quiritium Kolasa, 1973 from China.

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The Complete Plastid Genome of Magnolia zenii and Genetic Comparison to Magnoliaceae species

Molecules ◽

10.3390/molecules24020261 ◽

2019 ◽

Vol 24 (2) ◽

pp. 261 ◽

Cited By ~ 8

Author(s):

Yongfu Li ◽

Steven Paul Sylvester ◽

Meng Li ◽

Cheng Zhang ◽

Xuan Li ◽

...

Keyword(s):

Plastid Genome ◽

Sequence Data ◽

Genome Structure ◽

Phylogenetic Reconstruction ◽

Strong Support ◽

Gc Content ◽

Single Copy ◽

Protein Coding ◽

Critically Endangered Species ◽

Genomic Study

Magnolia zenii is a critically endangered species known from only 18 trees that survive on Baohua Mountain in Jiangsu province, China. Little information is available regarding its molecular biology, with no genomic study performed on M. zenii until now. We determined the complete plastid genome of M. zenii and identified microsatellites. Whole sequence alignment and phylogenetic analysis using BI and ML methods were also conducted. The plastome of M. zenii was 160,048 bp long with 39.2% GC content and included a pair of inverted repeats (IRs) of 26,596 bp that separated a large single-copy (LSC) region of 88,098 bp and a small single-copy (SSC) region of 18,757 bp. One hundred thirty genes were identified, of which 79 were protein-coding genes, 37 were transfer RNAs, and eight were ribosomal RNAs. Thirty seven simple sequence repeats (SSRs) were also identified. Comparative analyses of genome structure and sequence data of closely-related species revealed five mutation hotspots, useful for future phylogenetic research. Magnolia zenii was placed as sister to M. biondii with strong support in all analyses. Overall, this study providing M. zenii genomic resources will be beneficial for the evolutionary study and phylogenetic reconstruction of Magnoliaceae.

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Molecular analysis of selected paramphistome isolates from cattle in southern Africa

Journal of Helminthology ◽

10.1017/s0022149x15000905 ◽

2015 ◽

Vol 90 (6) ◽

pp. 784-788 ◽

Cited By ~ 3

Author(s):

S. Dube ◽

M.S. Sibula ◽

Z. Dhlamini

Keyword(s):

Sequence Data ◽

Animal Health ◽

Phylogenetic Reconstruction ◽

Morphological Characterization ◽

Its2 Sequence ◽

Molecular Techniques ◽

Its2 Rdna ◽

African Countries ◽

Rdna Sequences ◽

The Individual

AbstractParamphistomes are parasites of domestic and wild ruminants, the effects of which in animal health remain underestimated. Very few studies in Africa have been done using molecular techniques to resolve situations associated with taxonomical groupings and epidemiology of these parasites. In this study, the genetic variability of nine representative paramphistome isolates collected from southern African countries, namely Botswana, South Africa, Zambia and Zimbabwe, was assessed using both morphological and internal transcribed spacer 2 (ITS2) rDNA sequence data. Morphological characterization and identification were carried out using median sagittal sections of the paramphistomes. DNA of the individual paramphistomes was isolated, the ITS2 rDNA was amplified, purified and sequenced. The sequences were submitted to GenBank, which assigned them the following accession numbers: KP639631, KP639630, KP639632, KP639633, KP639634, KP639635, KP639636, KP639637 and KP639638. These sequences were used for phylogenetic analysis using MEGA 6. Morphological characterization revealed three species of paramphistomes belonging to three different sub-families: one Stephanopharynx compactus isolate, a member of the Stephanopharyngidae sub-family; one Carmyerius dollfusi isolate, a member of the Gastrothylacidae sub-family; and seven Calicophoron microbothrium isolates belonging to the Paramphistomidae sub-family. ITS2 sequence analysis using BlastN results indicated that this is the first report of S. compactus (KP639630) and C. dollfusi (KP639636). Phylogenetic reconstruction of the paramphistome isolates revealed three separate clades representing the three species. However, the clade with all the C. microbothrium isolates was the only one that was supported by a higher bootstrap value of 92%, although there was no differentiation of the isolates according to geographical locations. The low divergence values on the ITS2 sequences of the C. microbothrium isolates indicate that ITS rDNA sequences can be used as a molecular tool to infer knowledge for resolving taxonomic groupings.

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