Phylogeny of the neotropical moth tribe Josiini (Notodontidae: Dioptinae): comparing and combining evidence from DNA sequences and morphology

DNA sequences were gathered from mitochondrial COII and nuclear ribosomal 18S and 28S genes for 21 moth species in the tribe Josiini (Notodontidae: Dioptinae) and two outgroup genera. These data complement a previously published morphological character set for the same taxa. We examine whether relationships in the Josiini are best reflected by a single phylogenetic analysis of all the data, or by a consensus of separate trees generated from DNA and morphology. Even in cases where analyses of partitioned data produce incongruent cladograms, the underlying disagreement between partitions is relatively small. While both molecular and morphological data provide useful character information by themselves, we conclude that the best supported phylogenetic hypothesis is the one derived from combined analysis.     

Toward a Better Understanding of the Phylogeny of the Asplanchnidae (Rotifera)

We investigated the phylogenetic relationships of Family Asplanchnidae using both morphological and molecular data. The morphological database, comprising 23 characters from 19 taxa (15 Asplanchnidae and 4 outgroups), was compiled from a survey of the literature and our own observations; the molecular data (ITS and V4 region nuclear regions and mitochondrial cox1) was sequenced from specimens that we collected. Our analysis of the morphological data set (maximum parsimony) yielded 12 most-parsimonious trees with a tree length of 27 steps. From this analysis we conclude (1) Asplanchnidae is a monophyletic group as are the three genera comprising it, (2) there is no compelling support for the argument that Asplanchna should be separated into two discrete genera, and (3) there is some support for the proposal that Asplanchnidae and Synchaetidae are sister groups. Our analysis of the molecular data set supports the first two of these conclusions while the sister group of the family varied depending on the gene region analyzed and families and genera included. Current understanding of the phylogeny of Asplanchnidae is hampered by the need for additional informative morphological characters and a lack of molecular data for the genus Harringia and several other members of the Asplanchnidae.     

Once a Batesian mimic, not always a Batesian mimic: mimic reverts back to ancestral phenotype when the model is absent

Batesian mimics gain protection from predation through the evolution of physical similarities to a model species that possesses anti-predator defences. This protection should not be effective in the absence of the model since the predator does not identify the mimic as potentially dangerous and both the model and the mimic are highly conspicuous. Thus, Batesian mimics should probably encounter strong predation pressure outside the geographical range of the model species. There are several documented examples of Batesian mimics occurring in locations without their models, but the evolutionary responses remain largely unidentified. A mimetic species has four alternative evolutionary responses to the loss of model presence. If predation is weak, it could maintain its mimetic signal. If predation is intense, it is widely presumed the mimic will go extinct. However, the mimic could also evolve a new colour pattern to mimic another model species or it could revert back to its ancestral, less conspicuous phenotype. We used molecular phylogenetic approaches to reconstruct and test the evolution of mimicry in the North American admiral butterflies (Limenitis: Nymphalidae). We confirmed that the more cryptic white-banded form is the ancestral phenotype of North American admiral butterflies. However, one species, Limenitis arthemis, evolved the black pipevine swallowtail mimetic form but later reverted to the white-banded more cryptic ancestral form. This character reversion is strongly correlated with the geographical absence of the model species and its host plant, but not the host plant distribution of L. arthemis. Our results support the prediction that a Batesian mimic does not persist in locations without its model, but it does not go extinct either. The mimic can revert back to its ancestral, less conspicuous form and persist.     

Wing pattern evolution and the origins of mimicry among North American admiral butterflies (Nymphalidae: Limenitis)

The evolution of wing pattern diversity in butterflies has emerged as a model system for understanding the origins and maintenance of adaptive phenotypic novelty. Admiral butterflies (genus Limenitis) are an attractive system for studying wing pattern diversity because mimicry is common among the North American species and hybrid zones occur wherever mimetic and non-mimetic wing pattern races meet. However, the utility of this system has been limited because the evolutionary relationships among these butterflies remain unclear. Here I present a robust species-level phylogeny of Limenitis based on 1911 bp of two mitochondrial genes (COI and COII) and 904 bp of EF1-alpha for all five of the Nearctic species/wing pattern races, the majority of the Palearctic species, and three outgroup genera; Athyma, Moduza (Limenitidini), and Neptis (Limenitidinae: Neptini). Maximum-likelihood and Bayesian analyses indicate that the North American species are a well-supported, monophyletic lineage that is most closely related to the widespread, Palearctic, Poplar admiral (L. populi). Within North America, the Viceroy (L. archippus) is the basal lineage while the relationships among the remaining species are not well resolved. A combined maximum-likelihood analysis, however, indicates that the two western North America species (L. lorquini and L. weidemeyerii) are sister taxa and closely related to the wing pattern subspecies of the polytypic Limenitis arthemis species complex. These results are consistent with (1) an ancestral host-shift to Salicaceae by the common ancestor of the Poplar admiral and the Nearctic admiral lineage, (2) a single colonization of the Nearctic, and (3) a subsequent radiation of the North American forms leading to at least three independent origins of mimicry.     

Phylogenetic analysis of the tribe Bovini (Mammalia: Artiodactyla)

A matrix of 57 (mainly cranial) characters and 32 taxa of fossil and Recent Bovini (buffaloes, bison and cattle) has been analysed using the parsimony program HENNIG86. Among the best established results are the exclusion of Parabos , polyphyly of Leptobos , monophyly of the Bos sensu lato + buffaloes group (a clade including all Recent Bovini), probable monophyly of the Bubalina and Syncerina, and the close relationship between bison and yak. Some other interesting questions raised include the apparent absence of a close link between Pliocene African bovines (except Leptobos syrticus ) and later African buffaloes, and the possible monophyly of Pelorovis oldowayensis+Bos sensu lato .     

The first vespiform tineid moth (Lepidoptera: Tineidae)

Abstract Vespitinea gurkharum gen. et sp.n. is described from specimens reared from a bracket-fungus ( Ganoderma - Polyporaceae) from lowland rain-forest in Brunei. This striking wasp-like moth is suggested to be a Batesian mimic of species of Vespidae and Pompilidae (Hymenoptera) and the first example of this mimicry type recorded from the Tineoidea. Abdominal, eye and wing-coupling modifications suggest that it is diurnal and a behavioural mimic. The systematic position of Vespitinea is discussed with reference to biology and adult and larval morphology.     

Phylogeny of the tribe Colletieae, Rhamnaceae

A cladistic analysis based on 63 morphological characters was carried out on the tribe Colletieae including two presumed closely related genera, Geanothus and Noltea as outgroupS. In addition to a parsimony analysis of the equally weighted characters, analyses investigating the effects of character weighting, removal of a presumed hybrid species as well as the impact of uncertainly scored characters were undertaken. In all analyses Noltea was placed as sister group to a well supported monophyletic Colletieae. Nineteen different in group topologies were found, with the additional analyses mainly supporting two of them. Within the Colletieae a basal dichotomy divides Trevoa and Retanilla from the remainder of the tribe. While the Trevoa-Retanilla clade is fully resolved, the second lacks detailed resolution. Within this clade the Colletia species from a well supported monophyletic group, while monophyly of the disjunct genus Discaria could not be confirmed.     

Phylogeny of the tribe Antirrhineae (Scrophulariaceae) based on morphological andndhF sequence data

Phylogenetic relationships within the tribe Antirrhineae (Scrophulariaceae) are analysed and discussed on the basis of parsimony analyses of morphological andndhF gene sequence data. The results indicate that the tribe Antirrhineae consists of four major groups of genera, theAnarrhinum clade, theGambelia clade, theMaurandya clade, and theAntirrhinum clade. TheAnarrhinum clade, consisting of the Old World bee-pollinated generaAnarrhinum andKickxia, is sister to the rest of the tribe. TheGambelia clade consists of the New World generaGambelia andGalvezia, which are very closely related and pollinated by hummingbirds. TheMaurandya clade consists of one subclade includingMaurandya and a number of related bee- or hummingbird-pollinated New World genera and another subclade with the Old World bee-pollinated generaAsarina andCymbalaria. TheAntirrhinum clade consists mainly of bee-pollinated Old World genera, such asAntirrhinum, Linaria, Chaenorhinum, and their segregates, but also includes the New World generaMohavea andHowelliella, of which the latter is known to be partly pollinated by hummingbirds. It is concluded that hummingbirdpollination has evolved independently within Antirrhineae at least three times from bee-pollinated ancestors.     

The monophyly of the Characidiinae, a Neotropical group of characiform fishes (Teleostei: Ostariophysi)

Although virtually no phylogenetic evidence (in the sense advocated by Hennig, 1966) had been previously presented to support the monophyly of the Characidiinae, and most 'diagnostic' characters used by previous authors were found to be unacceptable in a cladistic classification, i t is still possible to diagnose the Characidiinae in a phylogenetic sense. This study revealed the existence of 13 synapomorphies supporting the monophyly of the group. Several of these synapomorphies, such as the modifications associated with the mesethmoid, the jaw bones, and the ribs of the fifth vertebra, are unique to the Characidiinae, thus providing a solid basis for recognizing the group as a monophyletic unit of characiform fishes. Demonstration of characidiin monophyly provides a solid foundation for further phylogenetic analysis of characidiin interrelationships, and higher level relationships among characiform fishes.     

Phylogeny of Australian species of flatheads (Teleostei, Platycephalidae) as determined by allozyme electrophoresis

Phylogenetic relationships of 24 taxa of Platycephalid fish were examined for up to 40 loci using starch and polyacrylarnide gel electrophoresis. Over 400 different enzyme mobilities were scored. The extent of homoplasy was estimated to be between 5 and 12%. Polymorphism at the 1% level was observed at 26 of the 40 loci. The importance of shared polymorphic alleles in cladistic analysis was endorsed by the different results obtained from multistate and binary coding of alleles. Many loci were shown to contain phylogenetically informative ancestral alleles which appear irregularly in extant species. The polymorphism parsimony method provided the most informative results. Genetic similarities between endemic Australian species from each family stem provide the basis for a major revision of subfamilies and genera within the family.     

Phylogeny reconstruction in the neogene bryozoan metrarabdotos: A paleontologic evaluation of methodology

An adequate stratigraphic record can not only aid in both cladistic and stratophenetic reconstruction of phytogenies, but can also serve in estimating the temporal consistency of the resulting phylogenetic trees. For hypothetical data sets, cladistically constructed trees can be as consistent with the temporal distribution of sampled populations or species as those constructed stratophenetically. Empirical testing in taxonomic groups with sufficiently dense fossil records is needed to show whether, and under what conditions, this potential can be realized. A stratophenetic tree and cladistic trees based on several approaches to character weighting were constructed for Caribbean Neogene species of the bryozoan Metrarabdotos with multiple‐character data from closely spaced sequential populations. The modular morphology and highly punctuated evolutionary pattern of these species blur the distinction between continuous and discrete characters, so that all available characters are potentially of equal significance in establishing phytogenies, rather than just those with discrete states conventionally used in cladistic analysis. However, only the cladistic trees generated with all characters weighted to emphasize contribution to species discrimination have temporal consistencies that are clearly significant statistically and approach that of the stratophenetic tree in magnitude. These results provide a start toward establishing general guidelines for cladistic analysis of taxa with stratigraphie records too sparse for stratophenetic reconstruction.     

Phylogeny and radiation of pollination systems in DISA (Orchidaceae)

We studied the patterns of adaptive radiation in Disa, a large orchid genus in southern Africa. A cladogram for 27 species was constructed using 44 morphological characters. Pollination systems were then mapped onto the phylogeny in order to analyze pathways of floral evolution. Shifts from one pollination system to another have been a major feature of the evolutionary diversification of Disa. Unlike many plant genera that are pollinated mainly by a single group of insects, radiation in Disa has encompassed nearly all major groups of pollinating insects; in all, 19 different specialized pollination systems have been found in the 27 species included in this analysis. Another striking pattern is the repeated evolution of broadly similar pollination systems in unrelated clades. For example, butterfly-pollinated flowers have evolved twice; showy deceptive flowers pollinated by carpenter bees, twice; long-spurred flowers pollinated by long-tongued flies, four times; night-scented flowers pollinated by moths, three times; and self-pollination, three times. This suggests that a few dominant pollinator species in a region may be sufficient to generate diversification in plants through repeated floral shifts that never retrace the same pathways.     

Phylogeny of the intertidal aleocharine tribe Liparocephalini (Coleoptera: Staphylinidae)

The tribe Liparocephalini (genera Liparocephalus Mäklin, 1853;Diaulota Casey, 1893 [ = Genoplectes Sawada, 1955];Paramblopusa Ahn & Ashe, Amblopusa Casey, 1893;Salinamexus Moore & Legner, 1977 [ = Biophytosus Moore & Legner, 1977]), all of which are exclusively restricted to the Pacific coasts of the Holarctic Region, is hypothesized to be a monophyletic group based on the following synapomorphies: seta v absent (inferred to be lost) from mentum (reversed one time in the Liparocephalus lineage), setae distributed only on mesal surface of galea and apex with setae, one medial seta present on prementum, and contiguous mesocoxal cavities. Natural history and history of the classification of the Liparocephalini are discussed. Phylogenetic analyses of the species of the Liparocephalini are presented based on larval (21 characters, 57 states), adult (49 characters, 115 states), and a combination of larval and adult characters (70 characters, 172 states). Analysis of the combined larval and adult data sets with successive approximation resulted in a single most parsimonious tree (length = 937, CI = 0.885, RI = 0.930) with the following patterns of generic relationships (outgroup (Salinamexus + Biophytosus (Amblopusa (Paramblopusa (Diaulota + Genoplectes, Liparocephalus))))).     

Moths of the tribe Pseudoterpnini (Geometridae: Geometrinae): a review of the genera

The classification of the genera of the widely distributed Old World tribe Pseudoterpnini is reviewed and 34 genera are recognized. Two new generic synonyms ( Sterictopsis Warren and Oxyphanes Turner as synonyms of Rhuma Walker), and 21 new or reinstated combinations are established. Representative moths of all the genera are illustrated in colour (upper side and underside), and genitalia of all genera are illustrated in monochrome (162 figures). All the known species and subspecies of Pseudoterpnini are listed (321), together with their synonyms. The Pseudoterpnini and their characters are assessed, and many genera are newly assigned to the tribe.  © 2007 Natural History Museum, London. Journal compilation © 2007 The Linnean Society of London, Zoological Journal of the Linnean Society , 2007, 150 , 343–412.     

Derived morphology in a basal moth: The uniquely specialized sternum V glands of Agathiphaga (Lepidoptera: Agathiphagidae)

The sternum V gland is a notable specialization shared by basal Lepidoptera and most Trichoptera; it is generally present in both sexes or in females only. In both orders the secretory cells usually discharge into a sac-like reservoir from which a duct leads to the opening on sternum V. In contrast, the gland in agathiphagid moths is only present in males and it exhibits several unique specialisations: the glandular portion being the apical (morphologically anterior) part of a long tubular cuticular invagination covered with contiguous ‘type-3’ glandular units; together with the following part of the efferent duct it is coiled like a ball of yarn; the duct expands into a fusiform reservoir, and a separate small sac surrounded by a complex muscular coat is present just inside the gland opening. The principal opener muscle of each gland originates on the contralateral side of sternum VI, hence crossing its counterpart in the midline. Characters of the agathiphagid sternum V gland, the function of which remains unclear (though sex pheromone production may appear most likely), add significantly to the suite of autapomorphies exhibited by this otherwise overall remarkably generalized moth taxon.     

Phylogeny of the Neotropical cichlid fish tribe Cichlasomatini (Teleostei: Cichlidae) based on morphological and molecular data, with the description of a new genus

Phylogenetic relationships among cichlasomatine cichlids were studied using an extensive taxon sampling and both morphological and molecular data sets. A new genus, Andinoacara n. gen. with six species ( A. pulcher-rivulatus group of previous authors) from trans-andean South America and NW cis-andean South America, is described based on results of phylogenetic and diagnosability analyses and tests of alternative topologies Our results demonstrate that cichlasomatine cichlid diversity is divided into five principal lineages composed of eleven genera and three suprageneric clades: the [( Bujurquina , Tahuantinsuyoa ), ( Andinoacara ) (BAT) clade; the ( Cleithracara , ( Nannacara , Ivanacara )] clade (NIC) plus Laetacara and 'Aequidens' hoehnei ; and the ( Aequidens , Cichlasoma ) clade, where Aequidens is paraphyletic to Cichlasoma . Two former Aequidens species are additionally transferred into Krobia ( K. potaroensis , K. paloemeuensis ). 'Aequidens' hoehnei probably represents a unique evolutionary lineage and would thus qualify for a separate generic status. Molecular data are yet not available for this species and its generic status requires further study. Relationships between the three suprageneric clades and between Acaronia and Krobia could not be convincingly resolved with our data set of two mitochondrial (16S and cyt b ) and two nuclear (S7 and RAG1) molecular markers and 96 morphological characters.     

Marine insects: genital morphology, phylogeny and evolution of sea skaters, genus Halobates (Hemiptera: Gerridae)

Five species of sea skaters, genus Halobates Eschscholtz, are the only insects to have successfully colonized the open ocean. In addition, 36 species are found in sheltered coastal waters throughout tropical Indo-Pacific. The taxonomy of the genus is relatively well known, but reliable hypotheses about phylogenetic relationships are required if the biogeography and evolution of sea skaters is to be discussed in a meaningful way. This work presents the results of a study of new characters from the genital segments, especially those of the male phallus and the female gynatrial complex, and a reinterpretation for several other characters. In total 64 characters were scored for 26 species of Halobates , two species ofAsclepios and one species of Metrocoris. With Asclepios and Metrocoris species as outgroups, the character state sets were analysed cladistically using the computer program Hennig86. After critical evaluations of both characters and clades, a phylogeny for Halobates is presented and its taxonomic implications are discussed. A number of monophyletic species groups are delimited. One genus-level synonymy and three species-level synonymies are suggested. The evolution of Halobates is discussed in the light of the reconstructed phylogeny and present knowledge of the ecology and behaviour of sea skaters. A hypothesis of ecological evolution in halobatine water striders is proposed and tested.     

Vertical stratification of ithomiine butterfly (Nymphalidae: Ithomiinae) mimicry complexes: the relationship between adult flight height and larval host-plant height

Data are presented which confirm previous findings that sympatric mimicry complexes dominated by unpalatable Neotropical ithomiine butterflies (Nymphalidae: Ithomiinae) are vertically stratified by height of flight. Flight height of ithomiine species is positively correlated with the height of their larval host-plants. Thus members of a mimicry complex utilize host-plants of similar heights. Non-mimetic British woodland butterflies also show a positive relationship between flight height and host-plant height, which suggests that the relationship is independent of mimicry. I propose that female butterflies fly at heights which maximize the probability of encountering their larval host-plants, and that males fly at similar heights to females in order to maximize the probability of encountering potential mates. Female butterflies probably encounter plants of similar heights to their larval hosts more frequently than they encounter plants of other heights. I suggest that butterfly species may therefore be more likely to make host shifts to plant species of a similar height to their current host-plants. Finally, I discuss how the relationship between flight height and height of larval host-plants, coupled with microhabitat-dependent selection on colour pattern, could lead to the evolution in sympatry of vertically stratified mimicry complexes.