Dna-Dna Hybridization Studies of Carnivorous Marsupials .2. Relationships Among Dasyurids (Marsupialia, Dasyuridae)

1990 ◽  
Vol 38 (6) ◽  
pp. 673 ◽  
Author(s):  
JAW Kirsch ◽  
C Krajewski ◽  
MS Springer ◽  
M Archer

A suite of comparisons among ten radiolabelled dasyurid species and one outgroup bandicoot was generated using the hydroxyapatite chromatography method of DNA-DNA hybridisation; comparisons were also made with four other dasyurid taxa. Square matrices of DELTA-T(m)s, DELTA-Modes, and DELTA-T50H's were complied and corrected for reciprocity, additivity, and, in the case of DELTA-T(m)'s, normalised percentages of hybridisation. These matrices were analysed using the FITCH algorithm in Felsenstein's PHYLIP (Version 3.1), and all distinct topologies were jackknifed to test for internal consistency. Additionally, uncorrected DELTA-T(m), DELTA-Mode, and DELTA-T50H datasets were bootstrapped and subjected to phylogenetic analysis to assess measurement imprecision. FITCH trees from folded matrices including unlabelled species or those for which heteroduplex comparisons were incomplete were also calculated and jack-knifed, both before and after correction. With the exception of limited measurements to Dasyuroides byrnei and Dasykaluta rosamondae, which showed affinities with Dasyurus spp., the final tree was fully resolved: Sminthopsis crassicaudata and S. murina, together with the more distant Planigale maculata, are the sister-group to all other dasyurids examined, which in turn comprise two clades. One of these includes Dasyurus, Dasyuroides, and Dasykaluta; the other, 'true' Antechinus (A. flavipes, A. stuartii, A. swainsonii) as a sister-group to Antechinus melanurus plus Murexia longicaudata, with Phascogale tapoatafa representing a probable sister-group to all Antechinus with Murexia. DNA-DNA hybridisation provides no support for the genus Satanellus: most of the trees linked Dasyurus albopunctatus with D. maculatus instead of D. hallucatus. Similarly, Antechinus flavipes and A. stuartii appear to be closer to each other than either is to A. swainsonii. The historical biogeographic significance of the adopted phylogeny is considered, and it is concluded that the putative early Miocene separation of Australia and New Guinea was probably too early to account for the independent evolution of the New Guinean clade.

1992 ◽  
Vol 40 (6) ◽  
pp. 563 ◽  
Author(s):  
D Edwards ◽  
M Westerman

The diprotodontian family Petauridae is composed of two subfamilies: Petaurinae (gliders) and Dactylopsilinae (striped possums). Leadbeater's possum (Gymnobelideus leadbeateri) has generally been placed among the petaurines on the basis of morphological, particularly dental, characters. Recent microcomplement fixation data, however, suggest that G. leadbeateri is a sister group to the Dactylopsilinae. We report DNA-DNA hybridisation comparisons among Leadbeater's possum, two dactylopsilines, two petaurines, and an outgroup pseudocheirid. Phylogenetic analysis of these data support the basic dichotomy between petaurines and dactylopsilines, and suggest that G. leadbeateri is more closely related to dactylopsilines. Resolution of this relationship, assayed by bootstrap analysis, is limited, but branch lengths on the optimal tree suggest a rapid initial diversification of three lineages within the Petauridae: dactylopsilines, petaurines and G. leadbeateri.


1995 ◽  
Vol 43 (4) ◽  
pp. 395 ◽  
Author(s):  
JAW Kirsch ◽  
TF Flannery ◽  
MS Springer ◽  
FJ Lapointe

We constructed DNA-hybridisation matrices comparing 18 genera of Megachiroptera and an outgroup microchiropteran, and eight species of Pteropus and two related genera. Three species each of Megachiroptera and Microchiroptera, two of Primates, and an outgroup armadillo were compared in another matrix; additional representatives of other mammalian orders figured in a further set of experiments. Among the megachiropterans examined, Nyctimene and Paranyctimene comprise the sister-group to other pteropodids. Of the 'macroglossines', only Macroglossus and Syconycteris are associated apart from typical pteropodines, while the four remaining nectar-feeders (Eonycteris, Megaloglossus, Melonycteris, Notopteris) are independently linked with non-nectar-feeding clades. Thus, Megaloglossus is the nearest relative of Lissonycteris, with Epomophorus and Rousettus successive sister-groups to both, while Eonycteris is the sister of all four; Melonycteris and Pteralopex form a trichotomy with the closely related Acerodon and Pteropus, and Notopteris is the sister-taxon to all four. It therefore appears that anatomical specialisations for nectar- and pollen-feeding evolved (or were lost) several times within Pteropodidae. Cynopterus and Dobsonia represent additional clades within the Pteropodinae, with which Thoopterus and Aproteles are respectively paired. Comparisons among species of Pteropus and related genera suggest that Acerodon may be congeneric with Pteropus, but that Pteralopex clearly is not. The ordinal-level matrices support bat monophyly: no order tested is closer to either of the chiropteran suborders than they are to each other, and bats are separated from Primates by at least two nodes. On the basis of previous rate determinations for mammals, we estimate that the African grouping (Epomophorus, Megaloglossus, Lissonycteris) is mid-Miocene in origin, that the two major pteropodid subfamilies (Nyctimeninae and Pteropodinae, including 'Macroglossinae') separated in the Early Miocene, and that the divergence of chiropteran suborders dates from the latest Cretaceous or earliest Palaeocene. Arrangement of genera within Pteropodidae supports the family's Australo-Pacific or south-east Asian origin.


2019 ◽  
Vol 75 (3-4) ◽  
pp. 397-411
Author(s):  
Jorge Morales ◽  
Oldřich Fejfar ◽  
Elmar Heizmann ◽  
Jan Wagner ◽  
Alberto Valenciano ◽  
...  

Abstract New Amphicyonidae fossil remains from the early Miocene site of Tuchořice (the Czech Republic) confirm the presence of a new Thaumastocyoninae taxon: Peignecyon felinoides n. gen. et n. sp. It is characterized by a peculiar combination of plesiomorphic and derived morphological traits. The new genus can be defined by a long and sharp mandible diastema, loss of mesial premolars (p2–p3), p4 with an inclined distally high main cuspid, moderate sectorial carnassial teeth, m1 with relict metaconid, and talonid and trigonid of similar width, and reduced M2 and m2. In the phylogenetic analysis the Thaumastocyoninae form a monophyletic group characterized by the start of the m2/M2 reduction, still moderate in Crassidia intermedia (von Meyer, 1849), but remarkable in the other species of the clade. Peignecyon felinoides already shows the advanced features defining the Thaumastocyoninae, and constitutes the sister group of the most specialized genera Tomocyon Viret, 1929b and Thaumastocyon Sthelin et Helbing, 1925. Consequently, it can be considered an excellent link between this group and the more primitive members of the tribe Ysengrini (Ysengrinia Ginsburg, 1966 and Crassidia Heizmannn et Kordikova, 2000). Peignecyon felinoides shows that the trend towards hypercarnivory had already emerged in the European early Miocene fauna, thus helping to understand the complex evolution of the Amphicyonidae during the Miocene.


The Condor ◽  
2005 ◽  
Vol 107 (2) ◽  
pp. 342-352 ◽  
Author(s):  
Gerald Mayr

Abstract A new taxon of the Cypselomorphae—the clade including nightjars, potoos, owlet-nightjars, and apodiform birds—is described from the middle Eocene of Messel in Germany. Phylogenetic analysis of 49 characters shows Protocypselomorphus manfredkelleri gen. et sp. nov. to be the sister group of all other cypselomorph taxa, although this placement was not robust to bootstrapping. As evidenced by its swift-like beak, long forearm, and reduced feet, P. manfredkelleri was hawking insects on the wing. Thus it adds a distinctive new taxon to the already diverse assemblage of Paleogene aerial insectivores, all of which belong to the Cypselomorphae. This strongly contrasts with the extant avifauna where many aerial insectivores belong to songbirds, and among the insectivorous cypselomorph taxa only swifts and nightjars are species rich and widely distributed. The diversity of aerial insectivores among the Cypselomorphae may have been reduced by food competition with songbirds, which do not become the dominant group of insectivorous birds before the early Miocene. Una Nueva Ave Cipselomorfa del Eoceno Medio de Alemania y la Diversificación Temprana de las Aves Insectívoras Aéreas Resumen. Se describe un nuevo taxón de Cypselomorphae, el clado que incluye a las familias Caprimulgidae, Nyctibiidae, Aegothelidae y a las aves apodiformes, del Eoceno medio de Messel en Alemania. Un análisis filogenético de 49 caracteres muestra que Protocypselomorphus manfredkelleri gen. et sp. nov. es el grupo hermano de los demás taxa de cipselomorfos, aunque esta posición no fue apoyada por el análisis de bootstrap. Como lo evidencia su pico tipo vencejo, antebrazo largo y patas pequeñas, P. manfredkelleri cazaba insectos al vuelo. Así, este hallazgo añade un nuevo taxón al grupo ya diverso de los insectívoros aéreos del Paleógeno, todos los cuales pertenecen al grupo de los cipselomorfos. Esto contrasta fuertemente con la avifauna actual, en que muchos insectívoros aéreos pertenecen al grupo de los paseriformes, mientras que de los taxa de insectívoros cipselomorfos sólo los apodiformes y caprimúlgidos presentan alta diversidad específica y se encuentran ampliamente distribuidos. La diversidad de los insectívoros aéreos en los cipselomorfos pude haberse reducido debido a la competencia por alimento con las aves paseriformes, las cuales no se transforman en el grupo dominante de aves insectívoras sino hasta el Mioceno temprano.


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.


2002 ◽  
Vol 80 (1) ◽  
pp. 94-99 ◽  
Author(s):  
Donald T Stewart ◽  
Neil D Perry ◽  
Luca Fumagalli

Previous morphological and cytological analyses have suggested that the arctic shrew (Sorex arcticus) as currently recognized may be two distinct species. Specifically, those studies demonstrated considerable differentiation between the putative subspecies S. a. maritimensis and one or both of the other two subspecies, S. a. arcticus and S. a. laricorum. Phylogenetic analysis of 546 base pairs of cytochrome b sequence data from 10 arctic shrews from across Canada indicates that maritimensis is the sister-group to arcticus + laricorum. Furthermore, there is considerable genetic divergence between maritimensis and the other two putative subspecies (~8–9%; Kimura's two-parameter distance). Given that maritimensis and arcticus + laricorum appear to be reciprocally monophyletic clades with considerable genetic divergence (i.e., greater than that between other recognized pairs of sister-species within the S. araneus–arcticus group), we propose that S. maritimensis be recognized as a distinct species. The proportion of third-position transversion substitutions between S. arcticus and S. maritimensis suggests that these two species shared a common ancestor approximately 2.4 million years ago.


1997 ◽  
Vol 67 (2) ◽  
pp. 125-141 ◽  
Author(s):  
Christopher C. Tudge

A phylogenetic analysis of selected anomuran, thalassinidean, and other decapod crustacean taxa, based on spermatozoal ultrastructural characters and spermatophore morphological characters, was performed and the following relationships of the taxa are elucidated from the trees produced. The Anomura are not a monophyletic assemblage, with the lomoid Lomis being exclusive of the remainder of the anomuran taxa, and the thalassinid Thalassina included in the anomuran clade. The synapomorphy joining the majority of the conventional anomuran taxa (Lomis excluded) is the cytoplasmic origin of the microtubular arms. When the palinurid and thalassinoid representatives are separately designated as outgroups, the Astacidea and Brachyura jointly formed a sister group to the Anomura. The superfamilies Thalassinoidea, Paguroidea, and Galatheoidea are not monophyletic groups. In all analyses the anomuran families Coenobitidae and Porcellanidae each form a monophyletic group. The paguroid family Diogenidae is paraphyletic, with the genera Clibanarius and Cancellus separate from a single clade containing the remaining diogenid genera. The families Paguridae and Parapaguridae form a monophyletic clade with the exception of Porcellanopagurus. The two representatives of the family Chirostylidae (Eumunida and Uroptychus) fail to associate with the other species in the Galatheoidea. The taxa in the family Galatheidae are not a monophyletic assemblage. The only investigated hippoid Hippa is portrayed as the sister group to the remainder of the anomuran taxa (with the exception of Lomis).


1992 ◽  
Vol 40 (4) ◽  
pp. 423 ◽  
Author(s):  
MS Springer ◽  
GM Mckay ◽  
KP Aplin ◽  
JAW Kirsch

Comparison among eight pseudocheirid species and two outgroup petaurids were made by means of the hydroxyapatite chromatography method of DNA hybridisation. Matrices of DELTAT(m) and DELTAT(m)H-C values were analysed with the FITCH algorithm in Felsenstein's PHYLIP (Version 3.3). Jackknifing and bootstrapping were applied to determine the stability of resulting topologies. All the phylogenetic analyses produced trees that support (1) the monophyly of the Pseudocheirus herbertensis complex, (2) the monophyly of Pseudocheirus, (3) a close relationship between Hemibelideus and Petauroides, and (4) a close relationship between Pseudochirops archeri and Pseudochirops cupreus. Rates of single-copy DNA evolution are slightly faster in Pseudocheirus, Hemibelideus, and Petauroides than in Pseudochirops. Hybridisation evidence also provides a framework for understanding the timing of the pseudocheirid radiation and suggests that the divergence between extant genera dates back to about 36 million years ago.


2005 ◽  
Vol 36 (2) ◽  
pp. 121-143 ◽  
Author(s):  
Pekka Vilkamaa ◽  
Heikki Hippa

AbstractThe phylogeny of the main groups of the Sciaroidea, including the fossil Antefungivoridae, Archizelmiridae, Mesosciophilidae, Pleciofungivoridae, Pleciomimidae, Protopleciidae and Bolitophilidae: Mangasinae, and an extant new taxon, was studied by parsimony analysis. Two cladistic analyses of seventy-eight morphological characters from adults were made. One analysis, with forty-one extant taxa in the ingroup and the other, with the addition of twelve fossil taxa, both produced two most parsimonious cladograms. The phylogenetic hypotheses obtained differed from each other, and in part also to a great extent from previous ones although most of the traditionally recognized groups appeared monophyletic, including the speciose Cecidomyiidae and Sciaridae. The Cecidomyiidae (fossil analysis) or the Keroplatidae-Ditomyiidae (extant analysis) appeared as the sister-group of the rest of the Sciaroidea. Following on from these analyses, we propose emending the current Sciaridae to include the following subfamilies: Archizelmirinae stat. n., Rangomaraminae stat. n., Sciarinae, Sciarosominae subfam. n. and Sciarotrichinae subfam. n. A new taxon from Namibia, Sciarotricha biloba gen. n., sp. n. is described, and, according to the phylogenetic analysis, is placed in the Sciaridae (Sciarotrichinae). The sister-group of the Sciaridae as newly defined is the Mycetophilidae group, in the extant analysis including the Mycetophilidae, Manotidae, Lygistorrhinidae, Pterogymnus and Sciaropota, and in the fossil analysis even including the Mesosciophilidae and the Ohakunea group (Ohakunea + Colonomyia).


2018 ◽  
Vol 69 (8) ◽  
pp. 2232-2235
Author(s):  
Marius Moga ◽  
Mark Edward Pogarasteanu ◽  
Antoine Edu

The role of arthroscopy in incipient and mild arthrosis, even combined with proximal tibial ostetomy, is well known and well documented. On the other hand, its role in the treatment of advanced arthrosis of the large joints, especially the knee, is a subject of controversy. The proponents of the use of arthroscopy in advanced arthrosis claim that meniscectomy, synovectomy, ostophytectomy, chondral lesion stabilization, arthroscopic release, plica and loose body removal greatly improve the quality of life for most patients, especially if followed by the use of viscoelastic injection, by diminishing pain and improving joint range of motion. The opponents claim that, even though the advantages are clear in the cases that refuse arthroplasty, in all the other cases the surgical indication should be total knee arthroplasty, as the clinical relief is temporary, but with all the risks of a surgical intervention. We have conducted an overview of the recent literature, in order to find objective evidence to sustain either point of view. We focused on articles published that included an objective measurement of before and after clinical status through clinical scores and objective measurements. We also focused on the follow-up period and on the evolution of the pathology after arthroscopy.


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