Gibson's reclassification of the enoplan nemerteans (Enopla, Nemertea): a critique and cladistic analysis

Gibson's (1988) reclassification of the class Enopla (phylum Nemertea), and in particular the forming of the taxon Paramonostilifera, is assessed by a cladistic analysis based on 35 characters. This analysis does not support the reclassification, and it is suggested that the previous classification is kept for the time being, although it is recognized that certain of the higher categories are non-monophyletic and should be reclassified.     

A new genus and species of monostiliferous hoplonemertean (Nemertea: Enopla: Monostilifera) from Japan

A new genus and species of monostiliferous hoplonemertean, Diopsonemertes acanthocephala gen. et sp. nov., is described from Otsuchi Bay, Japan. Significant anatomical features of the new form include a body wall longitudinal musculature anteriorly divided into inner and outer layers by connective tissue, no pre-cerebral septum, the presence of a thin coat of diagonal muscle fibres between the body wall longitudinal and circular muscle layers in the foregut body region, cephalic retractor muscles derived only from the inner portion of the divided longitudinal muscles and a rhynchocoel more than half the body length.     

Redescription and taxonomic reappraisal of Amphiporus elongatus Stephenson (Nemertea, Enopla) from the Firth of Clyde

Amphiporus elongatus Stephenson, 1911, is redescribed from histological studies of five specimens obtained from near the type locality. The systematic position of the species is reassessed and a new genus, Psammamphiporus , is established for it. Psammamphiporus elongatus (Stephenson) is so far known only from two intertidal sandy localities in the Firth of Clyde.     

The genus Valdivianemertes Stiasny-Wijnhoff 1923 (Nemertea,Enopla, Hoplonemertea): nomenclatural status and proper systematic position

The genus Akrostomum was erected by Grube in 1840 for a single species A. stannii which remained a nomen dubium until redescribed by Bürger in 1895 as Amphiporus stanniusi. Bürger (1909) described Drepanophorus valdiviae which shared many characters with A. stannii. Stiasny-Wijnhoff (1923) noted that these two forms belonged neither to Amphiporus nor Drepanophorus and united them in a new genus Valdivianemertes but did not mention the earlier name Akrostomum nor a family affiliation. Several major characters are examined. The nomenclatural status is analyzed, with retention of the junior synonym Valdivianemertes, and the type species is fixed as V. stannii by subsequent designation. Family affiliation is discussed, and the genus is transferred to the Cratenemertidae.     

A new genus and species of freshwater monostiliferous hoplonemertean (Nemertea, Enopla) from the People's Republic of China

A new genus and species of freshwater monostiliferous hoplonemertean, Limnemertes poyangensis gen. et sp. nov., from Poyang Lake, People's Republic of China, is described and illustrated. The taxon is compared and contrasted with previously described freshwater hoplonemerteans. This is the fourth species of freshwater nemertean to be described from China and the first recorded from Poyang Lake.     

Classification of the family Plectonemertidae (Nemertea): a phenetic comparison

A phenetic classification based on overall morphological similarity between the species in the family Plectonemertidae (genera Plectonemertes, Campbellonemertes, Potamonemertes, Leptonemertes, Katechonemertes, Argonemertes, Anliponemertes, and Acteonemertes ) was undertaken and the result compared with a cladistic and an evolutionary classification. Similarity between species was computed by Gower's general coefficient of similarity and various techniques were used to find patterns in the similarity matrix: single-linkage, average-linkage, and complete-linkage clustering, together with principal coordinate analysis. Although the explicit aim of phenetics is not to estimate the phylogeny, the classification based on overall similarity still portrays phylogeny better than an intuitive assessment of morphological similarity, as judged by the cladistic analysis. The classification does not support the previously proposed hypothesis that the two freshwater genera Campbellonemertes and Potamonemertes have descended from a terrestrial ancestor.     

A new genus and species of monostiliferoidean nemertean (Nemertea: Enopla) found on an egg mass of the anomuran decapod Paralithodes camtschatica

A new genus and species of monostiliferoidean enoplan nemertean from Alaska is described and illustrated. The nemertean, Alaxinus oclairi gen. et sp. nov. , was found on the egg mass of a red king crab, Paralithodes camtschatica.     

A new genus and species of monostiliferoidean nemertean (Nemertea: Enopla) found on an egg mass of the anomuran decapod Paralithodes camtschatica

A new genus and species of monostiliferoidean enoplan nemertean from Alaska is described and illustrated. The nemertean, Alaxinus oclairi gen. et sp. nov. , was found on the egg mass of a red king crab, Paralithodes camtschatica .     

Phylogeny and Cladistic Classification of the Paramonostiliferous Family Plectonemertidae (Phylum Nemertea)

Abstract— Numerical phylogenetic analysis of nemertean species from the genera Plectonemertes, Katechonemertes and Acteonementes (marine), Argonemertes, Antiponemertes and Leptonemertes (terrestrial), Potamonemertes and Campbellonemertes (freshwater) in the family Plectonemertidae was carried out with the following aims. (1) To estimate the evolutionary relationships between and among these species. (2) To lest the hypothesis of Moore and Gibson that the analysed freshwater species originated from a terrestrial ancestor. (3) To classify the species in monophyletic genera. The analysis did not confirm the hypothesis that the freshwater habitat has been colonised via land. Instead, it suggests that both terrestrial and freshwater species within this family have evolved from a marine ancestor. The cladogram suggests that Antiponemetes is paraphyletic, and it is combined with Argonemertes to form a monophyletic genus.     

Synamorphy,monophyly, and cladistic analysis: A reply to Wilkinson

Wilkinson (1991) suggests that the problems of polarity decisions and homoplasy in a cladistic analysis may be solved if cladists simply accept plesiomorphy as a reliable indicator of monophyly. Here we argue that: (1) Wilkinson's argument is based on misapprehension of synapomorphy and the problem of homoplasy; (2) His proposed methodology fails to consider the full ramifications of rooting, polarity, and parsimony; and (3) His method does not solve the problems he raises. We demonstrate the limitations of this methodology by using Wilkinson's practical example. We find no justification for the assertion that plesiomorphy may reliably delimit monophyly and recommend against Wilkinson's suggested methodological revisions.     

A cladistic analysis of the anomalocystitid mitrates

A cladistic analysis of the anomalocystitid mitrates is presented. A neutral terminology for the anomalocystitid skeleton is proposed, independent of the zoological interpretation of the fossils as echinoderms or as craniates. The anomalocystitid monophyly is supported by parsimony, although the instability of several basal taxa makes it difficult to ascertain the sequence in which characters were acquired or modified in the transition from the mi-trocystitids to the anomalocystitids. The genus Barrandeocarpus falls outside the anomalocystitids as traditionally defined in the literature, and is either polyphyletic or monophyletic. Diamphidiocystis drepanon is either a basal anomalocystitid or the sister taxon to the group ( Enoploura popei + Allanicytidiidae). Ateleocystites guttenbergensis is placed either at the base of the anomalocystitids or as the sister taxon to a group including mainly boreal forms, the only non-boreal members being the South African Bokkeveldia oosthuizeni and the Australian Victoriacystis wilkinsi.     

A cladistic analysis of Haemanthus and Scadoxus

Estimates, based on various cladistic methods, of the evolutionary relationship between the species of Haemanthus and Scadoxus are presented. The different methods are compared and discussed. On the data available the compatibility analysis gave a result easier to explain biologically compared to the parsimony analysis. In Haemanthus the results are ambiguous and more data needed. In Scadoxus the following sub–generic division is supported: Two subgenera, Scadoxus and Demeusea , the first with two sections, Scadoxus and Gyaxis , the second with three, Demeusea, Gamolepis and Choananthus.     

Homo floresiensis: a cladistic analysis

The announcement of a new species, Homo floresiensis, a primitive hominin that survived until relatively recent times is an enormous challenge to paradigms of human evolution. Until this announcement, the dominant paradigm stipulated that: 1) only more derived hominins had emerged from Africa, and 2) H. sapiens was the only hominin since the demise of Homo erectus and Homo neanderthalensis. Resistance to H. floresiensis has been intense, and debate centers on two sets of competing hypotheses: 1) that it is a primitive hominin, and 2) that it is a modern human, either a pygmoid form or a pathological individual. Despite a range of analytical techniques having been applied to the question, no resolution has been reached. Here, we use cladistic analysis, a tool that has not, until now, been applied to the problem, to establish the phylogenetic position of the species. Our results produce two equally parsimonious phylogenetic trees. The first suggests that H. floresiensis is an early hominin that emerged after Homo rudolfensis (1.86 Ma) but before H. habilis (1.66 Ma, or after 1.9 Ma if the earlier chronology for H. habilis is retained). The second tree indicates H. floresiensis branched after Homo habilis.     

A cladistic analysis ofAnisopappus (Asteraceae: Inuleae)

A cladistic analysis of the genusAnisopappus (Asteraceae: Inuleae) has been undertaken. A hypothesis of species interrelationships in the genus is presented for the first time. The analysis also includedArctotis (Arctoteae), used as outgroup, and five additional genera from theInuleae: Geigeria, Calostephane, Asteriscus, Buphthalmum, Pulicaria, andInula. It is concluded thatAnisopappus is a monophyletic group situated at the base of the tribe, diagnosed by, e.g., their obtuse stylar sweeping-hairs. The species with acute sweeping-hairs were found to be derived within the genus. Problems concerning species delimitation, biogeography and character evolution in the genus are briefly discussed.     

A new species of Tetrastemma (Nemertea: Enopla: Monostiliferoidea) from Ria de Foz, north-western Spain, found living in the mantle cavity of the bivalve mollusc Scrobicularia plana

A new species of monostiliferoidean nemertean, Tetrastemmafozensis , from the mantle cavity of the bivalve mollusc Scrobicularia plana , in the Ría de Foz, north-western Spain, is described and illustrated. Other nemerteans from the mantle cavity of Scrobicularia collected in Poole Harbour, southern England, are provisionally identified as conspecific with the Ria de Foz material, but show certain anatomical differences whose taxonomic significance cannot at present be assessed.     

A cladistic analysis of the nomadine bees (Hymenoptera: Apoidea)

Abstract. This study compares the results of Rozen's cladistic analysis of the larvae of fifteen genera of cleptoparasitic bees in the subfamily Nomadinae with an independent data set of adult characters for the same genera. Adult characters exhibited considerably higher levels of homoplasy and poorer resolution of cladistic relationships, with multiple equally parsimonious cladograms. However, comparison of a Nelson consensus tree based on adult characters with the cladogram based on larval characters reveals three components consistently supported in both analyses (the tribes Epeolini and Ammobatini, and Neopasites + Neolarra) , one component supported only by adult characters (Isepeolus + Protepeolus) , and one terminal component supported only by larval characters (Nomada + Ammobatini), as well as several more inclusive groupings based on larval characters that are difficult to compare with the adult consensus tree because it shows so much less resolution. When adult and larval characters are combined in a single data matrix, the resulting cladogram closely resembles the cladogram based on larval characters alone, although levels of homoplasy are considerably higher than in the larval analysis.
A preliminary analysis of adult characters for thirty-four genera in the Nomadinae also exhibited high levels of homoplasy and very large numbers of equally parsimonious cladograms. Nevertheless, certain consistent monophyletic groupings, most notably the Epeolini and Ammobatini, were also supported in this analysis. The one currently recognized tribe whose monophyly has received no support from any analysis is the Nomadini.
The relevance of these phylogenetic hypotheses to our understanding of host associations and variable features of egg morphology and oviposition behaviour in nomadine bees is briefly discussed.     

A cladistic analysis of interspecific relationships ofSaguinus

The dental and cranial morphologies of all species ofSaguinus, S. oedipus, S. geoffroyi, S. leucopus, S. nigricollis, S. fuscicollis, S. labiatus, S. mystax, S. imperator, S. bicolor, andS. midas are examined. The following hypotheses are developed by cladistic methodology, using only synapomorphic characters to assess the interspecific relationships ofSaguinus.Saguinus are divided into two main groups; one consists ofS. oedipus, S. geoffroyi, andS. leucopus, and the other includesS. inustus, S. nigricollis, S. fuscicollis, S. labiatus, S. mystax, S. imperator, S. bicolor, andS. midas. In the former group,S. oedipus is more closely related toS. geoffroyi than either is toS. leucopus. In the latter group,S. labiatus, S. mystax, andS. imperator are classified into one group, andS. bicolor andS. midas form one monophyletic group.