Phylogenetic relationships among families of the order Anomopoda (Crustacea, Branchiopoda, Cladocera)

Zootaxa ◽  
2004 ◽  
Vol 760 (1) ◽  
pp. 1 ◽  
Author(s):  
LOURDES M.A. ELMOOR-LOUREIRO

The phylogenetic relationships among families of the Order Anomopoda (Crustacea, Branchiopoda, Cladocera) were investigated through a cladistic analysis including 93 characters and 37 terminal taxa (2 as outgroups). The strict consensus tree supported the monophyly of the Anomopoda and its families, and indicated the existence of two main clades: (Moinidae+Daphniidae) and (Dumontidae (Ilyocryptidae+Bosminidae+Radopoda)). The later clade was supported by trunk limb characters, probably related to life associated with the bottom or with macrophytes (lifestyle lost in Bosminidae, but still visible in some of its trunk limbs). Within the Radopoda, the Eurycercoidea was monophyletic, but the monophyly of the Macrothricoidea was not supported.

Zootaxa ◽  
2009 ◽  
Vol 2022 (1) ◽  
pp. 1-14 ◽  
Author(s):  
RAFAEL LEMAITRE ◽  
PATSY A. MCLAUGHLIN ◽  
ULF SORHANNUS

Phylogenetic relationships within the “symmetrical” hermit crab family Pylochelidae were analyzed for 41 of the 45 species and subspecies currently considered valid. In the analyses, 78 morphological characters comprised the data matrix and the outgroup consisted of Thalassina anomala, a member of the Thalassinidae, and Munida quadrispina, a member of the Galatheidae. A poorly resolved strict consensus tree was obtained from a heuristic parsimony analysis of unweighted and unordered characters, which showed the family Pylochelidae and the subfamilies Pylochelinae and Pomatochelinae to be monophyletic taxa – the latter two groups had the highest Bremer support values. Additionally, while the subgenus Pylocheles (Pylocheles) was strongly supported, the subgenera Xylocheles, and Bathycheles were not. More fully resolved trees were obtained when using implied weighting, which recognized the monotypic subfamilies Parapylochelinae, Cancellochelinae and Mixtopagurinae. The subfamily Trizochelinae was found to have four distinct clades and several ambiguously placed taxa.


2000 ◽  
Vol 78 (3) ◽  
pp. 351-360 ◽  
Author(s):  
Ana M Arambarri

The diagnostic characters of the genus Lotus L. are a claw with a thickened infolded margin, diadelphous stamens, and a style hardened from the base. This genus contains about 100 species that are distributed throughout the world. To investigate the phylogeny of the Old World species of Lotus, subgenus Edentolotus, sections Krokeria, Xantholotus, and Erythrolotus, a cladistic analysis was performed using 31 morphological characters. To test the phylogenetic relationships among species of Lotus-Edentolotus and Dorycnium, Pedrosia, and Tetragonolobus, these taxa were included as part of the ingroup. The polarity of the characters was based on the outgroup comparison method, using Anthyllis as one outgroup and Tripodion as another. The analysis with Anthyllis as outgroup yielded eight equally parsimonious trees (with all characters equally weighted), each with 62 steps, a consistency index of 0.53, and a retention index of 0.75. All trees (including the strict consensus tree from the eight initial trees) showed that genus Lotus, subgenus Edentolotus, and sections Xantholotus and Erythrolotus are polyphyletic, with only section Krokeria appearing as monophyletic. On the other hand, the groups of species Lotus angustissimus, Lotus corniculatus, Lotus creticus, and Lotus peregrinus are monophyletic. Identical results were derived from the data matrix using Tripodion as the outgroup. Results are compared with previous cytogenetic and biochemical evidence.Key words: cladistic analysis, Fabaceae, Loteae, Lotus, Old World species, phylogeny.


2017 ◽  
Vol 15 (4) ◽  
Author(s):  
Maria Laura S. Delapieve ◽  
Pablo Lehmann A ◽  
Roberto E. Reis

ABSTRACT The discovery of three new taxa of Hypoptotopomatini with ambiguous generic assignment prompted a reanalysis of the phylogenetic relationships of the tribe. The analysis focused on a data matrix of 56 terminals and 107 morphological characters comprising the three new taxa, most species of Hypoptopoma and Otocinclus, and all other species of the tribe. The 162 maximally parsimonious trees of 382 steps, consistency index of 0.41, and retention index of 0.83 were then summarized in a strict consensus tree. The results confirm the monophyly of the Hypoptopomatini, recover four genera as monophyletic (Acestridium, Hypoptopoma, Niobichthys, and Otocinclus), revealed Hypoptopoma and Oxyropsis to be non-monophyletic; and revealed two new genera within Hypoptopomatini. Additionally, Otocinclus was found to be sister to a group with all remaining genera of the tribe; Acestridium and Niobichthys were found to be sister to each other and that clade sister to a group formed by ((Leptotocinclus + Hypoptopoma [part]) + (Nannoxyropsis (Oxyropsis + Hypoptopoma [part]))). Based on this framework, changes to the classification and the taxonomy of the Hypoptopomatini are suggested and the new taxa are described.


An account is given of the comparative morphology of the family Littorinidae, based on examination of 122 species, grouped into 32 subgenera. The shell, operculum and principal organ systems are described, and their phylogenetic significance assessed. A total of 53 characters, coded as 131 character states, were chosen for inclusion in a cladistic analysis of the phylogenetic relationships of the subgenera. This was performed by the program paup, using the principle of maximum parsimony. The outgroup for the analysis comprised representatives of the Pomatiasidae and Skeneopsidae. A consensus tree was obtained from cladograms with consistency indices of 0.408 (autapomorphies excluded).


Zootaxa ◽  
2009 ◽  
Vol 2082 (1) ◽  
pp. 1-84 ◽  
Author(s):  
ALEXEY A. KOTOV

A revision of the genus Leydigia Kurz, 1875 (Anomopoda, Cladocera, Branchiopoda) is presented. The list of all species-group nominal taxa consists of 34 published and 3 unpublished names. Of these, 12 species are accepted as valid: (1) Leydigia (Leydigia) leydigi (Schödler, 1863); (2) L. (L.) louisi Jenkin, 1934 with two subspecies L. louisi louisi Jenkin, 1934 and L. louisi mexicana Kotov, Elías-Gutiérrez et Nieto, 2003; (3) Leydigia (Neoleydigia) propinqua Sars, 1903; (4) L. (N.) australis Sars, 1885; (5) L. (N.) microps Sars, 1916; (6) L. (N.) sp. nov. from 'L. acanthocercoides' in Alonso, 1996; (7) L. (N.). macrodonta Sars, 1916; (8) L. (N.) acanthocercoides (Fischer, 1854); (9) L. (N.). laevis Gurney, 1927; (10) L. (N.) cf. ipojucae Brehm, 1939; (11) L. (N.) ciliata Gauthier, 1939; (12) L. (N.) cf. striata Birabén, 1939. Lectotypes are selected for 3, 5, 7, and 9. Exact identification of 10 and 12 is not possible without examination of material from type localities and neotype selection. As confirmed by examination of authors' type material, some taxa (Leydigia africana Gurney, 1904 and Leydigia ankammaraoi Prasad, Santa Kumari et Bose, 1985) prove to be junior synonyms of previously described species; species 8-12 form a compact acanthocercoides-group, with fine differences among members. A cladistic analysis for 13 studied taxa and 18 morphological characters resulted in four most-parsimonious trees (TL = 32; CI = 0.78), which differ only in the grouping of members of the L. acanthocercoides-group. A slightly polytomic strict consensus tree (the 50% majority rule bootstrap simulation led to a tree of similar topology to the contree), as well as some 'orthodox' ideas on the evolution of the genus (not contradicting each other), are used to subdivide the genus into two subgenera, Leydigia (Leydigia) Kurz, 1875 and Leydigia (Neoleydigia) subgen. nov. L. (N.) acanthocercoides is the type species of the latter. A key for the identification of well-known species of Leydigia is provided. The level of description of representatives of the genus Leydigia in different continents is estimated, and perspectives for further investigations are outlined.


Botany ◽  
2008 ◽  
Vol 86 (8) ◽  
pp. 938-967 ◽  
Author(s):  
Lynn J. Gillespie ◽  
Robert J. Soreng ◽  
Roger D. Bull ◽  
Surrey W.L. Jacobs ◽  
Nancy F. Refulio-Rodriguez

The worldwide temperate subtribe Poinae comprises the largest grass genus, Poa (500+ species), and multiple additional small genera. We explore generic boundaries and relationships among genera of Poinae using nuclear ribosomal internal transcribed spacer data (ITS) and plastid trnT–trnL–trnF (TLF) sequence data. ITS and TLF analyses are mostly congruent with regards to circumscription of genera, and with respect to relationships among Poinae genera, but tree structure is generally better supported among genera in the ITS strict consensus tree. ITS and TLF both support two main Poinae lineages: (i) Poa and (ii) a clade comprising all other sampled Poinae. Nine small genera were nested within the large Poa clade, including Aphanelytrum , Dissanthelium , and Tovarochloa , supporting inclusion of these as sections within Poa. In the second clade, three subclades support close relationships among Nicoraepoa , Hookerochloa , and Arctagrostis ; Arctophila and Dupontia ; and Apera , Bellardiochloa , and Ventenata . Genera of the related subtribes Alopecurinae, Cinninae, and Miliinae were mixed among or in part external to Poinae in different ways in ITS and TLF analyses, and only subtribe Puccinelliinae was strongly supported and monophyletic. ITS analyses supported placement of Catabrosella , Hyalopoa , and Paracolpodium in Puccinelliinae (no TLF data available). The position of Poa subgenus Arctopoa is incongruent between the two analyses: TLF data support inclusion within Poa and ITS data place it outside of Poa. Similarly, TLF data resolves the genus Aniselytron outside of Poa, whereas ITS data place it within Poa. Based on these results and a consideration of morphology, we recognize Arctopoa and Aniselytron as genera, probably of ancient hybrid origins. Nothogenus  × Duarctopoa is coined for Arctopoa × Dupontia, with a single nothospecies  × Duarctopoa labradorica . A new combination is provided for Poa subg. Sylvestres .


1998 ◽  
Vol 353 (1378) ◽  
pp. 2077-2151 ◽  
Author(s):  
B. C. Livezey

The order Gruiformes, for which even familial composition remains controversial, is perhaps the least well understood avian order from a phylogenetic perspective. The history of the systematics of the order is presented, and the ecological and biogeographic characteristics of its members are summarized. Using cladistic techniques, phylogenetic relationships among fossil and modern genera of the Gruiformes were estimated based on 381 primarily osteological characters; relationships among modern species of Grues (Psophiidae, Aramidae, Gruidae, Heliornithidae and Rallidae) were assessed based on these characters augmented by 189 characters of the definitive integument. A strict consensus tree for 20,000 shortest trees compiled for the matrix of gruiform genera (length = 967, CI = 0.517) revealed a number of nodes common to the solution set, many of which were robust to bootstrapping and had substantial support (Bremer) indices. Robust nodes included those supporting: a sister relationship between the Pedionomidae and Turnicidae; monophyly of the Gruiformes exclusive of the Pedionomidae and Turnicidae; a sister relationship between the Cariamidae and Phorusrhacoidea; a sister relationship between a clade comprising Eurypyga and Messelornis and one comprising Rhynochetos and Aptornis ; monophyly of the Grues (Psophiidae, Aramidae, Gruidae, Heliornithidae and Rallidae); monophyly of a clade (Gruoidea) comprising (in order of increasingly close relationship) Psophia , Aramus , Balearica and other Gruidae, with monophyly of each member in this series confirmed; a sister relationship between the Heliornithidae and Rallidae; and monophyly of the Rallidae exclusive of Himantornis . Autapomorphic divergence was comparatively high for Pedionomus , Eurypyga , Psophia , Himantornis and Fulica ; extreme autapomorphy, much of which is unique for the order, characterized the extinct, flightless Aptornis . In the species–level analysis of modern Grues, special efforts were made to limit the analytical impacts of homoplasy related to flightlessness in a number of rallid lineages. A strict consensus tree of 20,000 shortest trees compiled (length = 1232, CI = 0.463) confirmed the interfamilial relationships resolved in the ordinal analysis and established a number of other, variably supported groups within the Rallidae. Groupings within the Rallidae included: monophyly of Rallidae exclusive of Himantornis and a clade comprising Porphyrio (including Notornis ) and Porphyrula ; a poorly resolved, basal group of genera including Gymnocrex , Habroptila , Eulabeornis , Aramides , Canirallus and Mentocrex ; an intermediate grade comprising Anurolimnas , Amaurolimnas , and Rougetius ; monophyly of two major subdivisions of remaining rallids, one comprising Rallina (paraphyletic), Rallicula , and Sarothrura , and the other comprising the apparently paraphyletic ‘long–billed’ rails (e.g. Pardirallus , Cyanolimnas , Rallus , Gallirallus and Cabalus and a variably resolved clade comprising ‘crakes’ (e.g. Atlantisia , Laterallus and Porzana , waterhens ( Amaurornis ), moorhens ( Gallinula and allied genera) and coots ( Fulica ). Relationships among ‘crakes’ remain poorly resolved; Laterallus may be paraphyletic, and Porzana is evidently polyphyletic and poses substantial challenges for reconciliation with current taxonomy. Relationships among the species of waterhens, moorhens and coots, however, were comparatively well resolved, and exhaustive, fine–scale analyses of several genera ( Grus , Porphyrio , Aramides , Rallus , Laterallus and Fulica ) and species complexes ( Porphyrio porphyrio –group, Gallirallus philippensis –group and Fulica americana –group) revealed additional topological likelihoods. Many nodes shared by a majority of the shortest trees under equal weighting were common to all shortest trees found following one or two iterations of successive weighting of characters. Provisional placements of selected subfossil rallids (e.g. Diaphorapteryx , Aphanapteryx and Capellirallus ) were based on separate heuristic searches using the strict consensus tree for modern rallids as a backbone constraint. These analyses were considered with respect to assessments of robustness, homoplasy related to flightlessness, challenges and importance of fossils in cladistic analysis, previously published studies and biogeography, and an annotated phylogenetic classification of the Gruiformes is proposed.


Author(s):  
Tomomi Saito ◽  
Masatsune Takeda

The phylogenetic relationships within the family Spongicolidae were examined based on a cladistic analysis of 38 adult morphological characters with reference to two outgroup species of the family Stenopodidae. The strict consensus tree identified Microprosthema as the most basal genus, followed by Paraspongicola, Spongicola and the remaining genera. The Spongicoloides represents the most derived genus among spongicolids. The genera Spongicola, Spongicoloides and Spongiocaris should be redefined, because they formed paraphyletic clades. The cladogram indicates that symbiosis with the hexactinellid sponges is coincident with the loss of gills, exopods on maxillipeds 2 and 3, and with the loss of spination on carapace, pereopods, abdomen, tail fan etc. These losses in the spongicolids are thought to be secondarily derived in relation to their sponge-associated habitat.


Zootaxa ◽  
2011 ◽  
Vol 2801 (1) ◽  
pp. 27 ◽  
Author(s):  
PAVEL G. NEMKOV ◽  
MICHAEL OHL

A cladistic analysis of the digger wasp tribe Bembicini based on morphological characters is presented. The underlying data matrix comprises 64 terminal taxa (coded on genus-level) and 54 morphological characters. The resulting strict consensus tree was used as the basis for a revised subtribal classification of the Bembicini. Based on a previously published classification, we herewith propose a number of changes. The subtribe Spheciina Nemkov and Ohl, subtrib. nov. (comprising Ammatomus A. Costa 1859, Kohlia Handlirsch 1895, Sphecius Dahlbom 1843, and Tanyoprymnus Cameron 1905) is removed from Handlirschiina Nemkov and Lelej 1996. The subtribe Stictiellina Bohart and Horning 1971, stat. resurr. (composed of Chilostictia Gillaspy 1983, Glenostictia Gillaspy in Gillaspy, Evans, and Lin 1962, Microstictia Gillaspy 1963, Steniolia Say 1837, Stictiella J. Parker 1917, and Xerostictia Gillaspy 1963) is separated from Bembicina Latreille 1802. The subtribe Argogorytina Nemkov and Lelej 1996 (Argogorytes Ashmead 1899, Neogorytes Bohart in Bohart and Menke 1976, Paraphilanthus Vardy 1995) is synonymized with Exeirina Dalla Torre 1897, syn. nov. Finally, the subtribe Trichogorytina Nemkov and Pulawski 2009 (genus Trichogorytes Rohwer 1912 only) is synonymized with Gorytina Lepeletier de Saint Fargeau 1845, syn. nov. An updated identification key to the subtribes of the Bembicini is provided.


2007 ◽  
Vol 139 (3) ◽  
pp. 297-307 ◽  
Author(s):  
Željko Tomanović ◽  
Ehsan Rakhshani ◽  
Petr Starý ◽  
Nickolas G. Kavallieratos ◽  
Ljubiša Ž. Stanisavljević ◽  
...  

AbstractWe analyzed the phylogenetic relationships between eight Aphidius Nees and six Lysaphidus Smith species on the basis of 12 morphological characters by parsimony analysis. The consensus tree does not support the generic status of Lysaphidus. Aphidius iranicus, sp. nov., associated with Titanosiphon bellicosum Nevsky on Artemisia absinthium L. from Iran, is described. The new parasitoid species is described and illustrated by line drawings, and its diagnostic characters are discussed. The taxonomic position of the subgenus Tremblayia Tizado and Núñez-Pérez is also considered. Tremblayia and Lysaphidus are newly classified as synonyms of Aphidius. The following new or revised combinations are proposed: Aphidius adelocarinus Smith, comb. rev., A. ramythirus Smith, comb. rev., A. rosaphidis Smith, comb. rev., A. viaticus (Sedlag), comb. nov., A. arvensis (Starý), comb. nov., and A. erysimi (Starý), comb. nov.


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