Effect of larval rearing temperature on adult female morphology of Anopheles (Nyssorhynchus) albimanus (Diptera: Culicidae)

Summary

Time to pupation, percent survival to pupation, and percent adult emergence of Anopheles albimanus Wiedemann decreased at higher larval rearing temperature. Mosquitoes reared at 30°C experienced higher mortality during the pupal stage than did mosquitoes reared at 22°C. Analysis of variance revealed that wing length and costal wing spot patterns of adult female A. albimanus were affected by larval rearing temperature. Female A. albimanus reared at 22°C had longer wings, and larger basal pale + prehumeral pale, prehumeral dark, and humeral pale costal wing spots than did female siblings reared at 30°C. Female A. albimanus reared at 30°C had larger subcostal pale spots than did female siblings reared at 22°C. Analyses of 2x2 contingency tables indicated that sex ratio was independent of larval rearing temperature, whereas survival to the adult stage and coalescence of wing spots were not independent of rearing temperature. The need to examine stability of morphological characters under differing environmental conditions is discussed.     

Key to Dohrniphora males (Diptera: Phoridae) of the Australasian and Oriental Regions with descriptions of new species

A key to males of the Australasian and Oriental species of Dohrniphora is provided. Twenty-five new species are described and two new synonyms proposed.     

Association and description of males, females and larvae of two New Caledonian Xanthochorema species (Trichoptera: Hydrobiosidae) based on mitochondrial 16S and COI sequences

A method for associating larvae, females and males of Trichoptera is demonstrated for New Caledonian Hydrobiosidae species of the genus Xanthochorema, using cytochrome oxidase subunit I (COI) and 16S mitochondrial gene sequences. Two species, X. caledon Kimmins, 1953 and X. celadon Schmid, 1989 , previously with unknown larvae and undescribed females, were associated, and males, females and larvae of both species are described. Mitochondrial COI and 16S gene fragments are demonstrated to be useful for association of sexes and life stages of the two species, and distance measures show that the method is likely to also be useful for other species within the genus. The associations are well supported by high bootstrap and jackknife values.     

Key to Dohrniphora males (Diptera: Phoridae) of the Australasian and Oriental Regions with descriptions of new species

A key to males of the Australasian and Oriental species of Dohrniphora is provided. Twenty-five new species are described and two new synonyms proposed.     

Contribution to the knowledge of female west palaearctic Glyptotendipes Kieff. (Diptera, Nematocera, Chironomidae)

The characters of the genitalia of the females of Glyptotendipes glaucus (Meigen, 1818), Glyptotendipes pallens (Meigen, 1804), Glyptotendipes paripes (Edwards, 1929), Glyptotendipes gripekoveni (Kieffer, 1913), Glyptotendipes aequalis (Kieffer, 1922), Glyptotendipes barbipes (Staeger, 1839) and Glyptotendipes salinus Michailova, 1987 are described. A key for the identification of these species is given.The taxonomic status of Glyptotendipes aequalis is discussed.     

Revision of the subgenus Udamochiras of Melaloncha bee-killing flies (Diptera: Phoridae: Metopininae)

The genus Melaloncha Brues is defined and groundplan character states established based on outgroup comparison with Phalacrotophora Enderlein and Melittophora Brues. Major groupings within Melaloncha are recognized, and two subgenera are established: Udamochiras Enderlein (type species M. colossia (Enderlein)) and Melaloncha s.s. (type species M. pulchella Brues). Subgenus Udamochiras is revised and 42 species are recognized, including the following 33 new to science: M. anaticula , M. angustifrons , M. apicula , M. aprica , M. basella , M. biseta , M. brevicarina , M. carinata , M. compressicauda , M. exigua , M. falcata , M. flavilata , M. hamata , M. hansoni , M. horologia , M. individa , M. lobata , M. maculifrons , M. parkeri , M. paxilla , M. premordica , M. rhampha , M. rhypopoda , M. rostrata , M. sinuosa , M. spatula , M. spicula , M. triangularis , M. trua , M. valeria , M. vargasi , M. villosa , M. woodi . Melaloncha simillima Borgmeier is removed from synonymy with M. piliapex Borgmeier and reinstated as a separate species; lectotypes are designated for both.  © 2004 The Linnean Society of London, Zoological Journal of the Linnean Society , 2004, 140 , 1−42     

Phylogenies based on combined mitochondrial and nuclear sequences conflict with morphologically defined genera in the eimeriid coccidia (Apicomplexa)

Partial mitochondrial (mt) cytochrome c oxidase subunit I (COI) and near-complete nuclear (nu) 18S rDNA sequences were obtained from various eimeriid coccidia infecting vertebrates. New and published sequences were used in phylogenetic reconstructions based on nu 18S rDNA, mt COI and concatenated sequence datasets. Bayesian analyses of nu 18S rDNA sequences used secondary structure-based alignments with a doublet nucleotide substitution model; the codon nucleotide substitution model was applied to COI sequences. Although alignment of the mt COI sequences was unambiguous, substitution saturation was evident for comparisons of COI sequences between ingroup (eimeriid) and outgroup (sarcocystid) taxa. Consequently, a combined dataset applying partition-specific analytical and alignment improvements was used to generate a robust molecular phylogeny. Most eimeriid parasites that infect closely related definitive hosts were found in close proximity on the resulting tree, frequently in a single clade. Whether this represents coevolution or co-accommodation or a combination remains an open point. Unlike host associations, basic oocyst configuration (number of sporocysts per oocyst and sporozoites per sporocyst) was not correlated with phylogeny. Neither ‘Eimeria-type’ nor ‘Isospora-type’ oocyst morphotypes formed monophyletic groups. In the combined dataset tree (representing only a tiny fraction of described eimeriid coccidia), at least 10 clades of Eimeria spp. would need to be re-assigned to nine distinct genera to resolve their paraphyly. The apparent lack of congruence between morphotype and genotype will require taxonomists to balance nomenclatural stability and diagnostic ease against the ideal of monophyletic genera. For now, recognition of paraphyletic eimeriid genera defined by basic oocyst configuration may be necessary for reasons of taxonomic stability and diagnostic utility. Future taxonomic revisions to produce monophyletic eimeriid genera will ultimately require the identification of reliable phenotypic characters that agree with the molecular phylogeny of these parasites or, less optimally, acceptance that genotyping may be needed to support monophyletic supraspecific taxonomic groups.     

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.     

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.     

Phylogeny and classification of Muscini (Diptera, Muscidae)

Worldwide in distribution, the tribe Muscini comprises 21 accepted genera and about 350 species. In the present study, a cladistic analysis based upon adult morphological characters is carried out in order to discuss the monophyly of the tribe and its genera, the intergeneric relationships and, in some cases, also the intrageneric relationships. As a result, Muscini is supported as a monophyletic tribe sister-group of Stomoxyini. Except for Morellia Robineau-Desvoidy, Curranosia Paterson, and Eudasyphora Townsend, all the remaining genera are monophyletic. The results are dubious for Polietes Rondani, which was then provisionally kept unchanged. Morellia was broadened to include the Neotropical endemic genera Parapyrellia Townsend, Trichomorellia Stein, and Xenomorellia Malloch. Therefore, a new classification is proposed for Morellia in which it is divided into four subgenera: Morellia s.s. , Parapyrellia , Trichomorellia , and Xenomorellia . Furthermore, the previously proposed subgenus Dasysterna Zimin is given new status as a genus; however, as it is preoccupied by Dasysterna Dejean, the new replacement name Ziminellia nom. nov. is proposed herewith. Eudasyphora was found to be a paraphyletic group relative to Dasyphora Robineau-Desvoidy; both genera are hence synonymized, and Dasyphora is classified in three subgenera: Dasyphora s.s. , Eudasyphora , and Rypellia Malloch. The analysis demonstrated that the traditional classification of Musca Linnaeus into subgenera is artificial and, moreover, that the use of characters from male genitalia could be strongly informative for classifying the genus in phylogeny-supported species groups. Finally, the new classification proposal for Muscini recognizes 18 genera and, furthermore, two undescribed genus-ranked taxa are indicated.  © 2007 The Linnean Society of London, Zoological Journal of the Linnean Society , 2007, 149 , 493–532.     

Systematics of the spider genus Metabus O. P.-Cambridge, 1899 (Araneoidea: Tetragnathidae) with additions to the tetragnathid fauna of Chile and comments on the phylogeny of Tetragnathidae

The spider genus Metabus (Tetragnathidae) previously included nine species: the type M. gravidus O. P.-Cambridge, 1899 – junior synonym of Leucauge ocellata (Keyserling) – from Central America and eight species from Chile. In this paper, the classification of the Metabus species-complex is revised, and two new genera, with three new species and five new combinations, are described. Allende gen. nov. is created for four Chilean species not congeneric with the type of Metabus : the type A. puyehuensis sp. nov. , A. patagiatus (Simon) comb. nov. , A. nigrohumeralis (F. O. P.-Cambridge) comb. nov. and A. longipes (Nicolet) comb. nov. Further additions to the Chilean fauna are under the new genus Mollemeta gen. nov. – created for M. edwardsi (Simon) comb. nov. – and three new species of Chrysometa : C. acinosa sp. nov. , C. levii sp. nov. and C. maitae sp. nov. Metabus now includes four species: M. ocellatus (Keyserling) comb. nov. , M. debilis (O. P.-Cambridge) comb. nov. , M. ebanoverde sp. nov. and M. conacyt sp. nov. All of these species were included in a phylogenetic analysis of 38 tetragnathid and 12 orbicularian outgroup terminals scored for 105 morphological and behavioural characters. The results suggest that Metabus as previously circumscribed is polyphyletic. The phylogenetic relationships within tetragnathids are briefly discussed. © 2007 The Linnean Society of London, Zoological Journal of the Linnean Society , 2007, 151 , 285–335.     

Phylogenetic relationships in rhinonyssid mites (Acari: Rhinonyssidae) based on mitochondrial 16S rDNA sequences

A 390 bp region of the 16S rDNA gene was sequenced from six species ofrhinonyssid mites (Tinaminyssus columbae, T. minisetosum, Sternostomaturdi, S. sternahirundo, S. fulicae and Ptilonyssus euroturdi) andtwo subspecies (Tinaminyssus melloi melloi andTinaminyssus melloi streptopeliae) to examine the level ofsequence variation and the taxonomic levels to show utility in phylogenyestimation. Furthemore, two different geographic locations of T. m.melloi and T. m. streptopeliae were analyzed todetect variation between populations. Molecular data revealed the existence oftwo distinct groups in the genus Tinaminyssus parasitic oncolumbiform birds. These results are in agreement with those reported by someauthors using morphological characters. Sternostoma turdi parasitizing aerial birds appeared to be phylogenetically separated from otherspecies of this genus isolated from aquatic birds. Moreover, our studyaddressesthe validity of the subspecies status of T. melloistreptopeliae. This region of the mitochondrial 16S rDNA gene is auseful marker for inferring phylogenetic relationships among closely relatedrhinonyssid species, but not for more distantly related taxa.     

Phylogeny and classification of tribe Aedini (Diptera: Culicidae)

The phylogeny and classification of tribe Aedini are delineated based on a cladistic analysis of 336 characters from eggs, fourth‐instar larvae, pupae, adult females and males, and immature stage habitat coded for 270 exemplar species, including an outgroup of four species from different non‐aedine genera. Analyses of the data set with all multistate characters treated as unordered under implied weights, implemented by TNT version 1.1, with values of the concavity constant K ranging from 7 to 12 each produced a single most parsimonious cladogram (MPC). The MPCs obtained with K values of 7–9 were identical, and that for K = 10 differed only in small changes in the relationships within one subclade. Because values of K < 7 and > 10 produced large changes in the relationships among the taxa, the stability of relationships exemplified by the MPC obtained from the K = 9 analysis is used to interpret the phylogeny and classification of Aedini. Clade support was assessed using parsimony jackknife and symmetric resampling. Overall, the results reinforce the patterns of relationships obtained previously despite differences in the taxa and characters included in the analyses. With two exceptions, all of the groups represented by two or more species were once again recovered as monophyletic taxa. Thus, the monophyly of the following genera and subgenera is corroborated: Aedes, Albuginosus, Armigeres (and its two subgenera), Ayurakitia, Bothaella, Bruceharrisonius, Christophersiomyia, Collessius (and its two subgenera), Dahliana, Danielsia, Dobrotworskyius, Downsiomyia, Edwardsaedes, Finlaya, Georgecraigius (and its two subgenera), Eretmapodites, Geoskusea, Gilesius, Haemagogus (and its two subgenera), Heizmannia (and subgenus Heizmannia), Hopkinsius (and its two subgenera), Howardina, Hulecoeteomyia, Jarnellius, Kenknightia, Lorrainea, Macleaya, Mucidus (and its two subgenera), Neomelaniconion, Ochlerotatus (subgenera Chrysoconops, Culicelsa, Gilesia, Pholeomyia, Protoculex, Rusticoidus and Pseudoskusea), Opifex, Paraedes, Patmarksia, Phagomyia, Pseudarmigeres, Rhinoskusea, Psorophora (and its three subgenera), Rampamyia, Scutomyia, Stegomyia, Tanakaius, Udaya, Vansomerenis, Verrallina (and subgenera Harbachius and Neomacleaya), Zavortinkius and Zeugnomyia. In addition, the monophyly of Tewarius, newly added to the data set, is confirmed. Heizmannia (Mattinglyia) and Verrallina (Verrallina) were found to be paraphyletic with respect to Heizmannia (Heizmannia) and Verrallina (Neomacleaya), respectively. The analyses were repeated with the 14 characters derived from length measurements treated as ordered. Although somewhat different patterns of relationships among the genera and subgenera were found, all were recovered as monophyletic taxa with the sole exception of Dendroskusea stat. nov. Fifteen additional genera, three of which are new, and 12 additional subgenera, 11 of which are new, are proposed for monophyletic clades, and a few lineages represented by a single species, based on tree topology, the principle of equivalent rank, branch support and the number and nature of the characters that support the branches. Acartomyia stat. nov. , Aedimorphus stat. nov. , Cancraedes stat. nov. , Cornetius stat. nov. , Geoskusea stat. nov. , Levua stat. nov. , Lewnielsenius stat. nov. , Rhinoskusea stat. nov. and Sallumia stat. nov., which were previously recognized as subgenera of various genera, are elevated to generic status. Catageiomyia stat. nov. and Polyleptiomyia stat. nov. are resurrected from synonymy with Aedimorphus, and Catatassomyia stat. nov. and Dendroskusea stat. nov. are resurrected from synonymy with Diceromyia. Bifidistylus gen. nov. (type species: Aedes lamborni Edwards) and Elpeytonius gen. nov. (type species: Ochlerotatus apicoannulatus Edwards) are described as new for species previously included in Aedes (Aedimorphus), and Petermattinglyius gen. nov. (type species: Aedes iyengari Edwards) and Pe. (Aglaonotus) subgen. nov. (type species: Aedes whartoni Mattingly) are described as new for species previously included in Aedes (Diceromyia). Four additional subgenera are recognized for species of Ochlerotatus, including Oc. (Culicada) stat. nov. (type species: Culex canadensis Theobald), Oc. (Juppius) subgen. nov. (type species: Grabhamia caballa Theobald), Oc. (Lepidokeneon) subgen. nov. (type species: Aedes spilotus Marks) and Oc. (Woodius) subgen. nov. (type species: Aedes intrudens Dyar), and seven are proposed for species of Stegomyia: St. (Actinothrix) subgen. nov. (type species: Stegomyia edwardsi Barraud), St. (Bohartius) subgen. nov. (type species: Aedes pandani Stone), St. (Heteraspidion) subgen. nov. (type species: Stegomyia annandalei Theobald), St. (Huangmyia) subgen. nov. (type species: Stegomyia mediopunctata Theobald), St. (Mukwaya) subgen. nov. (type species: Stegomyia simpsoni Theobald), St. (Xyele) subgen. nov. (type species: Stegomyia desmotes Giles) and St. (Zoromorphus) subgen. nov. (type species: Aedes futunae Belkin). Due to the unavailability of specimens for study, many species of Stegomyia are without subgeneric placement. As is usual with generic‐level groups of Aedini, the newly recognized genera and subgenera are polythetic taxa that are diagnosed by unique combinations of characters. The analysis corroborates the previous observation that ‘Oc. (Protomacleaya)’ is a polyphyletic assemblage of species.     

The shieldbug genus Parastrachia and its position within the Pentatomoidea (Insecta: Hemiptera)

A new hemipteran subfamily, Parastrachiinae , is proposed in the Cydnidae for the single genus Parastrachia Distant 1883. There are two included species, P. japonensis (Scott 1880) and P. nagaensis Distant 1908. The morphology, relationships, and taxonomic history of Parastrachia are discussed     

Justification for the generic status of Courtoisina (Cyperaceae)

In the past, the two species of Courtoisina were placed either in Cyperus L., Mariscus Vahl, or in Courtoisia Nees (now Courtoisina Sojak). While these species show undoubted external similarities to both Cypm and Muriscus , they differ by their widely winged glumes and the arrangement of the veins of the glumes. They also differ profoundly from Mariscus and most species of Cypm in anatomical characteristics, and it is concluded that these differences warrant separate generic status.     

Phylogeny and systematics of the Acrapex apicestriata (Bethune-Baker, 1911) species complex (Lepidoptera,Noctuidae, Noctuinae,Apameini, Sesamiina) with the description of eight new species from the Afrotropics

Twelve morphologically similar species of Acrapex Hampson 1894, (Lepidoptera, Noctuidae, Noctuinae, Apameini, Sesamiina), from Western, Central and Eastern Africa are reviewed. Eight of these species are new to science and are described: Acrapex akunamatata n. sp. and A. incrassata n. sp. from Kenya; A. gracilis n. sp., A. iringa n. sp., A. lukumbura n. sp. and A. rungwe n. sp. from Tanzania; A. soyema n. sp. from Ethiopia; and A. zoutoi n. sp. from Benin. All 12 species belong to a species complex that we hereby define as the Acrapex apicestriata group. Host-plants for three of the new species are recorded: Setaria incrassata (Hochst.) Hack. for Acrapex incrassata; Cymbopogon pospishilii (K. Schum.) C.E. Hubb. for A. rungwe; and Andropogon perligulatus Stapf. for A. zoutoi. We also conducted molecular phylogenetic analyses (using maximum likelihood and Bayesian inference) on a six gene multimarker molecular dataset (four mitochondrial and two nuclear gene fragments; 4581 nucleotides in length) consisting of 15 Acrapex species (including seven species from the apicestriata group) and four outgroups species from the subtribe Sesamiina (from genera Busseola Thurau 1904, Sciomesa Tams & Bowden 1953, Pirateolea Moyal, Le Ru, Conlong, Cugala, Defabachew, Matama-Kauma, Pallangyo & Van den Berg 2010 and Sesamia Boisduval & Guenée 1852). Both maximum likelihood and Bayesian inference analyses yield a similar and well-supported topology, which supports the monophyly of the apicestriata group.     

New morphological characters for classifying Phoridae (Diptera) from the structure of the thorax

Forty‐six characters, mostly of the thoracic pleuron, are proposed for the reconstruction of the phylogenetic relationships among the major groups of the family Phoridae. Analysis of these characters, in conjunction with the pre‐existing suite of morphological characters from other body parts, provides a basis for a strongly supported new classification of the Phoridae, in which Sciadocerinae is the sister group of ((Chonocephalus Wandolleck & Cyphocephalus Borgmeier) + (Termitoxeniinae + (Metopininae + Phorinae s.l.))). A new subfamily, Chonocephalinae subfamily nov. , is proposed for Chonocephalus and Cyphocephalus, and a new genus, Hirotophora gen. nov. , is proposed for Chaetopleurophora multiseriata (Aldrich) ( comb. nov. ). © 2015 The Linnean Society of London     

Taxonomic classification of the reef coral family Lobophylliidae (Cnidaria: Anthozoa: Scleractinia)

Lobophylliidae is a family‐level clade of corals within the ‘robust’ lineage of Scleractinia. It comprises species traditionally classified as Indo‐Pacific ‘mussids’, ‘faviids’, and ‘pectiniids’. Following detailed revisions of the closely related families Merulinidae, Mussidae, Montastraeidae, and Diploastraeidae, this monograph focuses on the taxonomy of Lobophylliidae. Specifically, we studied 44 of a total of 54 living lobophylliid species from all 11 genera based on an integrative analysis of colony, corallite, and subcorallite morphology with molecular sequence data. By examining coral skeletal features at three distinct levels – macromorphology, micromorphology, and microstructure – we built a morphological matrix comprising 46 characters. Data were analysed via maximum parsimony and transformed onto a robust molecular phylogeny inferred using two nuclear (histone H3 and internal transcribed spacers) and one mitochondrial (cytochrome c oxidase subunit I) DNA loci. The results suggest that micromorphological characters exhibit the lowest level of homoplasy within Lobophylliidae. Molecular and morphological trees show that Symphyllia, Parascolymia, and Australomussa should be considered junior synonyms of Lobophyllia, whereas Lobophyllia pachysepta needs to be transferred to Acanthastrea. Our analyses also lend strong support to recent revisions of Acanthastrea, which has been reorganized into five separate genera (Lobophyllia, Acanthastrea, Homophyllia, Sclerophyllia, and Micromussa), and to the establishment of Australophyllia. Cynarina and the monotypic Moseleya remain unchanged, and there are insufficient data to redefine Oxypora, Echinophyllia, and Echinomorpha. Finally, all lobophylliid genera are diagnosed under the phylogenetic classification system proposed here, which will facilitate the placement of extinct taxa on the scleractinian tree of life.     

Molecular phylogeny of the subfamily Tephritinae (Diptera: Tephritidae) based on mitochondrial 16S rDNA sequences

The phylogeny of the subfamily Tephritinae (Diptera: Tephritidae) was reconstructed from mitochondrial 16S ribosomal RNA gene sequences using 53 species representing 11 currently recognized tribes of the Tephritinae and 10 outgroup species. The minimum evolution and Bayesian trees suggested the following phylogenetic relationships: (1) monophyly of the Tephritinae was strongly supported; (2) a sister group relationship between the Tephritinae and Plioreocepta was supported by the Bayesian tree; (3) the tribes Tephrellini, Myopitini, and Terelliini (excluding Neaspilota) were supported as monophyletic groups; (4) the non-monophyletic nature of the tribes Dithrycini, Eutretini, Noeetini, Tephritini, Cecidocharini, and Xyphosiini; and (5) recognition of 10 putative tribal groups, most of which were supported strongly by the statistical tests of the interior branches. Our results, therefore, convincingly suggest that an extensive rearrangement of the tribal classification of the Tephritinae is necessary. Since our sampling of taxa heavily relied on the current accepted classification, some lineages identified by the present study were severely under-sampled and other possible major lineages of the Tephritinae were probably not even represented in our dataset. We believe that our results provide baseline information for a more rigorous sampling of additional taxa representing all possible major lineages of the subfamily, which is essential for a comprehensive revision of the tephritine tribal classification.