Family revision and cladistic analysis of the Nereidoidea (Polychaeta : Phyllodocida)

1993 ◽  
Vol 7 (6) ◽  
pp. 1551 ◽  
Author(s):  
CJ Glasby

A family revision and cladistic analysis of the superfamily Nereidoidea sensu George and Hartmann - Schroder, 1985 (Polychaeta : Phyllodocida) based on internal and external morphological characters is presented. The superfamily, presently lacking synapomorphies, contains the Antonbruunidae, Calamyzidae, Hesionidae, Levidoridae, Nautiliniellidae, Nereididae, Pilargidae and Syllidae. Three synapomorphies are proposed: anterior or, rarely, anteroventral palps; paired pharyngeal retractor muscles; and the presence of metanephromixia. On the basis of this definition, the Chrysopetalidae are moved to the Nereidoidea. The requirement for ingroup monophyly necessitated synonymising the Antonbruunidae with the Pilargidae, and the Calamyzidae and Levidoridae with the Syllidae. The Nautiliniellidae are redefined. The cladistic analysis using 15 characters (21 apomorphic character states) and 3 outgroups (Aphroditidae, Polynoidae, and Sigalionidae) produced 3 minimum-length cladograms each with 29 steps and consistency index of 0.72. The cladograms showed the Nereidoidea to consist of 2 monophyletic groups: the Nereididae - (Chrysopetalidae - Hesionidae) and the Pilargidae - Nautiliniellidae - Syllidae. The topology of the latter group was variable; one cladogram had the Pilargidae as the sister-group of the Nautiliniellidae and Syllidae, and another had the Syllidae as the sister-group of the Nautiliniellidae and the Pilargidae. Evolutionary scenarios for multistate characters are given, and the phylogenetic relationships of taxa are discussed.

Zootaxa ◽  
2019 ◽  
Vol 4551 (2) ◽  
pp. 101 ◽  
Author(s):  
K. J. DAVID ◽  
S. RAMANI

The tribe Dacini comprising four genera, namely Bactrocera Macquart, Dacus Fabricius, Monacrostichus Bezzi and Zeugodacus Hendel, is a derived lineage in Tephritidae. It is one of the most economically important tribes in Tephritidae harbouring several species of quarantine concern across the world. We describe two new species of Bactrocera Macquart, B. (Parazeugodacus) conica David & Ramani, sp. n. & B. (B.) prabhui David, sp. n. from India. Postabdominal structures of males and/or females of 23 species of Bactrocera, 16 species of Zeugodacus and 8 species of Dacus from India are illustrated and described for the first time, which revealed similarities between Dacus and Zeugodacus with respect to epandrial shape and praeputium patterning. Bactrocera is unique in possessing oval shaped epandrium and an unpatterned praeputium. An analysis of phylogenetic relationships between three genera of the tribe Dacini from India based on morphological characters has been attempted for the first time. Cladistic analysis employing 51 characters of 62 species in Dacini, with seven species as outgroups revealed the monophyly of Dacini, Bactrocera and Dacus with supporting nonhomplasious synapomorphies. Ichneumonopsis Hardy, often included in the Gastrozonini, does not possess any synapomorphies of Dacini, eventhough it appeared at the base of the Dacini clade. Zeugodacus was retrieved as a monophyletic sister-group to Dacus based solely on a single homoplasious host plant character, with weak statistcal support. 


2005 ◽  
Vol 19 (6) ◽  
pp. 531 ◽  
Author(s):  
Faye Christidis

Phylogenetic relationships among the Australian Leptophlebiidae genera and selected genera from South America and New Zealand were investigated using a cladistic analysis of 43 morphological characters. The outcomes of this analysis were largely consistent with the higher-level relationships previously proposed by Pescador and Peters (1980). The monophyly of the Meridialaris lineage (comprising Austrophlebioides, Tillyardophlebia, Kirrara, ‘WT sp. 1’ and ‘WT sp. 2’ from Australia, Meridialaris from South America and Deleatidium and Atalophlebioides from New Zealand) was strongly supported, as was the monophyly of the Nousia lineage (Nyungara, Nousia and Koorrnonga). However, Australian genera assigned to the Hapsiphlebia lineage (Atalophlebia, Kalbaybaria, Ulmerophlebia, Jappa and Atalomicria) did not form a monophlyletic group. There was support for a sister-group relationship between the Dactylophlebia and Meridialaris lineages, and for the placement of Garinjuga (Penaphlebia lineage) as the sister-group to a large clade comprising genera of the Nousia, Dactylophlebia and Meridialaris lineages. The phylogenetic analysis provided some clarification of the affinities of Neboissophlebia, Bibulmena, Loamaggalangta and Kaninga. These genera appear to belong to lineages not recognised previously among the Gondwanan Leptophlebiidae.


2013 ◽  
Vol 27 (1) ◽  
pp. 129
Author(s):  
Edilson Caron ◽  
Cibele S. Ribeiro-Costa ◽  
Alfred F. Newton

Rove beetles of the genus Piestus Gravenhorst, 1806 are commonly captured under the bark of or inside decaying logs from Neotropical forests. Piestus belongs to the subfamily Piestinae, historically an ill-defined dumping-ground for Staphylinidae defined by plesiomorphic characters, but which has gradually been restricted in concept and currently includes only six additional extant genera worldwide. Piestinae in this restricted sense has been considered a probably monophyletic subfamily, but its status and phylogenetic position, as a possible sister-group of Osoriinae within the recently proposed Oxyteline group of staphylinid subfamilies, are uncertain and need confirmation. The main aim of the present study was to provide a morphological cladistic analysis and complete taxonomic revision of Piestus, which, as the type and most speciose genus of Piestinae, is critical for future phylogenetic studies involving the subfamily. In our study, the monophyly of Piestus is established and phylogenetic relationships among its species are proposed based on 70 adult morphological characters. Piestus is supported by 11 synapomorphies and high branch support. All species of Piestus are revised and the genus is redefined. The genus contains 43 species, including 13 species described here for the first time. The previously proposed subgenera Antropiestus Bernhauer, 1917, Eccoptopiestus Scheerpeltz, 1952, Elytropiestus Scheerpeltz, 1952, Lissopiestus Scheerpeltz, 1952, Piestus s. str., Trachypiestus Scheerpeltz, 1952 and Zirophorus Dalman, 1821 have not been confirmed, as they were found to be poly- or paraphyletic, or are here removed from Piestus, and therefore subgenera are not used. The main taxonomic changes are as follows. Lissopiestus, syn. nov. is proposed as new synonym of Eleusis Laporte, 1835 and its species, E. interrupta (Erichson, 1840), comb. rest., is transferred again to that genus. Antropiestus, syn. nov. and Eccoptopiestus, syn. nov. are proposed as new synonyms of Hypotelus Erichson, 1839 and their species, H. laevis (Solsky, 1872), comb. nov. and H. andinus (Bernhauer, 1917), comb. nov., are transferred to Hypotelus. Fourteen new synonymies are proposed (valid species listed first): P. lacordairei Laporte, 1835 = Z. furcatus Sharp, 1887, syn. nov.; P. capricornis Laporte, 1835 = P. frontalis Sharp, 1876, syn. nov.; P. pennicornis Fauvel, 1864 = P. plagiatus Fauvel, 1864, syn. nov.; P. rectus Sharp, 1876, syn. nov.; P. pygialis Fauvel, 1902, syn. nov.; P. surinamensis Bernhauer, 1928, syn. nov.; P. minutus Erichson, 1840 = P. nigrator Fauvel, 1902, syn. nov.; P. sulcatus Gravenhorst, 1806 = P. sanctaecatharinae Bernhauer, 1906, syn. nov.; P. condei Wendeler, 1955, syn. nov.; P. gounellei Fauvel, 1902 = P. wasmanni Fauvel, 1902, syn. nov.; P. mexicanus Laporte, 1835 = P. alternans Sharp, 1887, syn. nov.; P. aper Sharp, 1876 = P. schadei Scheerpeltz, 1952, syn. nov.; P. angularis Fauvel, 1864 = P. crassicornis Sharp, 1887, syn. nov.; H. andinus (Bernhauer, 1917) = P. strigipennis Bernhauer, 1921, syn. nov. One species is revalidated: P. fronticornis (Dalman, 1821), stat. rev., and one synonym is restored: P. penicillatus (Dalman, 1821) = P. erythropus Erichson, 1840, syn. rest. Neotypes are designated for P. lacordairei Laporte, 1835 and Oxytelus bicornis Olivier, 1811, and lectotypes are designated for P. puncticollis Fauvel, 1902, P. capricornis variety muticus Fauvel, 1902, P. zischkai Scheerpeltz, 1951, P. pennicornis Fauvel, 1864, P. plagiatus Fauvel, 1864, P. pygmaeus Laporte, 1835, P. niger Fauvel 1864, P. minutus Erichson, 1840, P. nigratror Fauvel, 1902, P. sulcatus Gravenhorst, 1806, P. sanctaecatharinae Bernhauer, 1906, P. sulcipennis Scheerpeltz, 1952, P. aper Sharp, 1876, P. schadei Scheerpeltz, 1952 and P. andinus Bernhauer, 1917.


2002 ◽  
Vol 80 (11) ◽  
pp. 1887-1899 ◽  
Author(s):  
Alison M Murray ◽  
Kathlyn M Stewart

The family Alestidae (also referred to as the African Characidae) comprises the African dwarf forms ("Petersiini") and the genera Alestes, Brycinus, Bryconaethiops, and Hydrocynus. Although several authors have presented characters to support the monophyly of the family, a cladistic analysis of the group has not been published. Furthermore, the interrelationships of the constituent groups are the subject of some controversy. A cladistic analysis of the Alestidae is presented, including characters to support the monophyly of the family. The results of this study indicate that several species should be removed from the genus Brycinus, that Hydrocynus is the sister group of Alestes s.str. (containing only five species), and that the dwarf alestids ("Petersiini") do not form a monophyletic group.


Zootaxa ◽  
2009 ◽  
Vol 2264 (1) ◽  
pp. 1-22 ◽  
Author(s):  
ADALGISA GUGLIELMINO ◽  
CHRISTOPH BÜCKLE

A small sector of Northern Apennines the Tuscan-Emilian Apennines constitutes an interesting diversity centre of a new Verdanus species group closely related to V. bensoni and the V. limbatellus group. It consists of three species: V. tyrannus sp. nov., V. saurosus sp. nov. and V. rosaurus sp. nov., the latter with two subspecies, V. rosaurus rosaurus ssp. nov. and V. rosaurus rex ssp. nov., which doubtless form a monophyletic group (V. rosaurus group). Data on their distribution, ecology and life cycle are added to their original descriptions. The new taxa live allopatrically in a very restricted area and thus occupy a distribution gap of another species group of Verdanus, the V. abdominalis group, present in Italy in the mountain regions of the Alps and Central and Southern Apennines. A hypothesis of the origin of the new taxa is presented based on the ecological conditions in the Tuscan-Emilian Apennines during the last Postglacial period and on the limited dispersal ability of these normally brachypterous insects. Possible synapomorphic characters and phylogenetic relationships of the new taxa with each other and with V. bensoni (China) and the V. limbatellus group (V. limbatellus (Zetterstedt), V. kyrilli (Emeljanov), V. sichotanus (Anufriev), V. kaszabi (Dlabola)) are discussed and a cladistic analysis is conducted. Comparing V. bensoni and the V. limbatellus group on the one hand and the V. rosaurus group on the other, some morphological characters appear to change often in parallel on the same paths, independently from the phylogenetic hypothesis. Remarkably, within the same morphological characters the range of variation among species inhabiting the comparatively minute area of the Tuscan-Emilian Apennines is similar to that found among other taxa distributed across vast areas of northern and central Eurasia.


2012 ◽  
Vol 46 (6) ◽  
pp. 31-48
Author(s):  
K. B. Sukhomlin

Abstract Phylogenetic relationships among the Palaearctic genera of the subfamily Simuliinae are analyzed based on the matrix of 100 morphological characters and 37 taxa, including 6 outgroups. Parsimonic analysis was resulted in 3 consensus trees (weighting based on CI, RI and RC indices) of slightly different topology, which show monophyly of the subfamily Simuliinae, tribes Stegopternini, Nevermanniini, Wilhelmiini and Simuliini, and a possible sister-group relationships between the latter two tribes. Tribe Ectemniini is apparently a paraphyletic formation. The analysis also supports transferring of the Stegopternini and Nevermanniini from Prosimuliinae to Simuliinae.


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.


Zootaxa ◽  
2007 ◽  
Vol 1530 (1) ◽  
pp. 19-26 ◽  
Author(s):  
MÁRCIA SOUTO COURI ◽  
CLAUDIO JOSÉ BARROS DE CARVALHO ◽  
PETER LÖWENBERG-NETO

This study presents a cladistic analysis of the Neotropical Philornis species based on morphological characters of adults and larvae, as well as biological data on larvae. Forty-one species of Philornis were used in the analysis, which was based on a total of 64 characters and included six outgroup taxa, half of which belong to Passeromyia Rodhain & Villeneuve, an Old World genus that shows the same variety of associations with birds as Philornis. Four most parsimonious cladograms (242 steps in length; ci=30; ri=69) were produced. According to the analysis, the genus Philornis is supported by the following synapomorphies (adults): only the pre-scutellar pair of acrostichal postsutural setae developed and setulae on anepimeron present. The resulting phylogenetic hypothesis (strict consensus) shows a basal polytomy that includes the species that traditionally correspond to the “aitkeni-group”. This group is mainly defined by male characters, which are known for only about half of these species. The next clade is divided into two others, the first one supported by the homoplasies: cheek hairs yellow; setulae on anepimeron black on upper half and yellow on lower half and proepimeral hairs yellow. This group traditionally corresponds to the “falsificus-group” and more data on the biology of the species will certainly clarify and/or confirm their relationships. Philornis downsi Dodge & Aitken is the sister group of all the remaining Philornis species. This third clade corresponds to the “angustifrons-group”, defined in this analysis by the following synapomorphies: concave shape of posterior end of puparium and the median width of female frons. These “traditional” groups, the relationships among the species and their evolutionary trends are discussed.


Author(s):  
Christopher J. Glasby ◽  
Patricia A. Hutchings ◽  
Kathryn Hall

A phylogenetic analysis of the polychaete clade Terebelliformia (Terebellida) was undertaken in order to test monophyly of families and subfamilies and to determine their affinities. Parsimony analyses of 41 terebelliform species with outgroup Owenia fusiformis and 46 morphological characters yielded 106–144 most parsimonious trees with length 250, consistency index=0·432, retention index=0·659 and rescaled consistency index=0·285. Monophyly was indicated for Alvinellidae, Ampharetidae, Terebellidae and Trichobranchidae and the terebellid subfamily Polycirrinae. Monophyly of Terebellidae is supported by the presence of a ridge-like tentacular membrane. Monophyly of Polycirrinae is supported by the loss of branchiae, trilobed upper lip, pinnate secondary notochaetae and ventro-lateral pads. Recognition of Polycirrinae renders taxa in the other terebellid subfamilies—Terebellinae and Thelepodinae—paraphyletic. Our results do not support previous classifications that placed Trichobranchidae as a subfamily of Terebellidae; rather it should be considered equal in rank with Alvinellidae, Ampharetidae, Terebellidae and Pectinariidae. The following relationships were obtained: (Trichobranchidae ((Alvinellidae, Ampharetidae) (Pectinariidae, Terebellidae))). This is the first time a Pectinariidae–Terebellidae sister group relationship has been found; it is supported by the synapomorphic presence of ventral glandular shields.


1995 ◽  
Vol 43 (6) ◽  
pp. 557 ◽  
Author(s):  
MS Springer ◽  
LJ Hollar ◽  
JAW Kirsch

Andersen's 1912 monograph on megachiropterans remains the definitive work on the systematics of this group. Andersen argued that the Macroglossinae, containing the eonycterine and notopterine sections, are a monophyletic sister-group to other fruitbats (i.e. Andersen's Rousettus, Cynopterus and Epomophorus sections). Two recent molecular studies (DNA hybridisation and restriction mapping of ribosomal cistrons), as well as an analysis of female reproductive characters, challenge the monophyly of the Macroglossinae and several of Andersen's other conclusions such as the phylogenetic position of Nyctimene. We performed a cladistic analysis on 36 morphological characters, including 33 that were gleaned from Andersen, to determine whether phylogenetic hypotheses based on modem phylogenetic methods are in agreement with Andersen's original conclusions and to compare morphological and molecular phylogenetic hypotheses. Minimum-length trees based on parsimony are largely consistent with Andersen and support (1) a monophyletic Macroglossinae, within which the eonycterine section is paraphyletic with respect to a monophyletic notopterine section, (2) a monophyletic Cynopterus section, excepting the exclusion of Myonycteris, (3) a monophyletic Epomophorus section, excepting the exclusion of Plerotes, and (4) a paraphyletic Rousettus section, with several of the Rousettus-like forms branching off near the base of the tree. Bootstrapping analyses on a reduced data-set that included taxa shared in common with the DNA hybridisation study did not provide strong support (greater than or equal to 95%) for any clades but did provide moderate support (greater than or equal to 70) for several clades, including a monophyletic Macroglossinae. These findings are in marked contrast to the DNA hybridisation phylogeny. A high index of between-data-set incongruence is further evidence for the clash between DNA hybridisation and morphology. A phylogenetic framework was constructed on the basis of morphological data and DNA hybridisation data using a criterion of moderate support and shows little resolution, whereas employing a criterion of strong support produced a framework resolving several additional nodes. One implication of this framework is that characteristic macroglossine features such as a long tongue with a thick carpet of filiform papillae have evolved independently on several occasions (or evolved once and were lost several times). Rates of character evolution for the morphological characters employed in our analysis were calculated using divergence times estimated from DNA hybridisation data. Rates have apparently been fastest in the interior branches, and slower along the external branches, which suggests an early adaptive radiation in the history of fruitbats.


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