87 research outputs found

    Placing the Fijian Honeyeaters within the meliphagid radiation: implications for origins and conservation

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    Understanding the evolutionary relationships of threatened species provides an important framework for making decisions about their conservation. However, unrecognised problems with the underlying phylogenetic analyses may bias the decision-making process. Recent phylogenetic studies have improved our understanding of Meliphagidae, but also indicate discordance between molecular datasets. Here, we examine the causes of this discordance using maximum likelihood tree-building and network analyses of identically sampled datasets for four genetic loci. Our results suggest that while we can be reasonably confident of relationships within species groups, discordance within and between molecular datasets tends to obscure relationships towards the base of the meliphagid tree. This ongoing uncertainty likely reflects differences in the sampling of markers and taxa between previously published analyses. To avoid the problems of conflicting data we used divergence time analyses of only the most densely sampled marker, NADH-ubiquinone oxidoreductase chain 2, to investigate the age and origins of the Fijian Meliphagidae. Our analyses suggest two temporally distinct colonisations of the Fijian archipelago. The large-bodied honeyeaters arrived ,15.6 million years ago, subsequently diversifying and spreading to Tonga and Samoa. In contrast, Myzomela appears to have arrived within the last 5.0 million years. The phylogenetic results therefore imply that conserving the evolutionary diversity of Meliphagidae in Polynesia requires that effort be spread across both the currently recognised taxa and geographical range

    Exploring Phylogeographic Congruence in a Continental Island System

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    A prediction in phylogeographic studies is that patterns of lineage diversity and timing will be similar within the same landscape under the assumption that these lineages have responded to past environmental changes in comparable ways. Eight invertebrate taxa from four different orders were included in this study of mainland New Zealand and Chatham Islands lineages to explore outcomes of island colonization. These comprised two orthopteran genera, one an endemic forest-dwelling genus of cave weta (Rhaphidophoridae, Talitropsis) and the other a grasshopper (Acrididae, Phaulacridum) that inhabits open grassland; four genera of Coleoptera including carabid beetles (Mecodema), stag beetles (Geodorcus), weevils (Hadramphus) and clickbeetles (Amychus); the widespread earwig genus Anisolabis (Dermaptera) that is common on beaches in New Zealand and the Chatham Islands, and an endemic and widespread cockroach genus Celatoblatta (Blattodea). Mitochondrial DNA data were used to reconstruct phylogeographic hypotheses to compare among these taxa. Strikingly, despite a maximum age of the Chathams of ~4 million years there is no concordance among these taxa, in the extent of genetic divergence and partitioning between Chatham and Mainland populations. Some Chatham lineages are represented by insular endemics and others by haplotypes shared with mainland populations. These diverse patterns suggest that combinations of intrinsic (taxon ecology) and extrinsic (extinction and dispersal) factors can result in apparently very different biogeographic outcomes

    Diversity and distribution of <i>Pleioplectron </i>Hutton cave wētā (Orthoptera: Rhaphidophoridae: Macropathinae), with the synonymy of <i>Weta</i> Chopard and the description of seven new species

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    The genus Pleioplectron was first described by Hutton (1896) and included six New Zealand species. This genus has since had three species moved, one each to the genera Pachyrhamma Brunner von Wattenwyl, 1888, Miotopus Hutton, 1898 and Novoplectron Richards, 1958. Here we clarify the status and appearance of Pleioplectron simplex Hutton, 1896 (incl. P. pectinatum Hutton, 1896 syn. nov.) and P. hudsoni Hutton, 1896, as well as P. thomsoni (Chopard, 1923) comb. nov., which is transferred from the genus Weta Chopard, 1923. The genus Weta is newly synonymised with Pleioplectron. We also describe seven new species of Pleioplectron from South Island, New Zealand: P. auratum sp. nov., P. caudatum sp. nov, P. crystallae sp. nov., P. flavicorne sp. nov., P. gubernator sp. nov., P. rodmorrisi sp. nov and P. triquetrum sp. nov. We base these descriptions on morphology using fresh specimens of both male and female adults, and provide support for each with DNA sequence variation (mtDNA, partial COI).</p

    High alpine sorcerers: revision of the cave wētā genus &lt;i&gt;Pharmacus&lt;/i&gt;Pictet &amp; de Saussure (Orthoptera: Rhaphidophoridae: Macropathinae), with the descriptionof six new species and three new subspecies

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    The New Zealand alpine cave wētā genus Pharmacus was first described by Pictet &amp; de Saussure (1893) as a monotypic taxon. Three species were added to the genus by Richards in 1972. Here we clarify the status and appearance of all known species of Pharmacus. Based on morphology and mtDNA sequences we determine that the species Pharmacus brewsterensis Richards, 1972 is better placed within the genus Notoplectron Richards, 1964. We also resolve the species Isoplectron cochleatum Karny, 1935 and show that it belongs to the genus Pharmacus. Additionally, we describe six new species and three new subspecies from the southern regions of South Island, New Zealand. We provide key traits and known distributions for all known species and subspecies in this alpine genus. New combinations: Pharmacus brewsterensis Richards, 1972 becomes Notoplectron brewsterense (Richards, 1972) comb. nov.; Isoplectron cochleatum Karny, 1935 becomes Pharmacus cochleatus (Karny, 1935) comb. nov. New species and subspecies: Pharmacus cochleatus rawhiti subsp. nov., Pharmacus cochleatus fiordensis subsp. nov., Pharmacus cochleatus nauclerus subsp. nov., Pharmacus concinnus sp. nov., Pharmacus cristatus sp. nov., Pharmacus notabilis sp. nov., Pharmacus perfidus sp. nov., Pharmacus senex sp. nov. and Pharmacus vallestris sp. nov. New synonyms: Pharmacus dumbletoni Richards, 1972 = Pharmacus montanus Pictet &amp; de Saussure, 1893 syn. nov.; Pharmacus chapmanae Richards, 1972 = Pharmacus cochleatus (Karny, 1935) syn. nov.</p

    Diversity and distribution of Pleioplectron Hutton cave wētā (Orthoptera: Rhaphidophoridae: Macropathinae), with the synonymy of Weta Chopard and the description of seven new species

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    The genus Pleioplectron was first described by Hutton (1896) and included six New Zealand species. This genus has since had three species moved, one each to the genera Pachyrhamma Brunner von Wattenwyl, 1888, Miotopus Hutton, 1898 and Novoplectron Richards, 1958. Here we clarify the status and appearance of Pleioplectron simplex Hutton, 1896 (incl. P. pectinatum Hutton, 1896 syn. nov.) and P. hudsoni Hutton, 1896, as well as P. thomsoni (Chopard, 1923) comb. nov., which is transferred from the genus Weta Chopard, 1923. The genus Weta is newly synonymised with Pleioplectron. We also describe seven new species of Pleioplectron from South Island, New Zealand: P. auratum sp. nov., P. caudatum sp. nov, P. crystallae sp. nov., P. flavicorne sp. nov., P. gubernator sp. nov., P. rodmorrisi sp. nov and P. triquetrum sp. nov. We base these descriptions on morphology using fresh specimens of both male and female adults, and provide support for each with DNA sequence variation (mtDNA, partial COI)

    High alpine sorcerers: revision of the cave wētā genus Pharmacus Pictet & de Saussure (Orthoptera: Rhaphidophoridae: Macropathinae), with the description of six new species and three new subspecies

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    The New Zealand alpine cave wētā genus Pharmacus was first described by Pictet & de Saussure (1893) as a monotypic taxon. Three species were added to the genus by Richards in 1972. Here we clarify the status and appearance of all known species of Pharmacus. Based on morphology and mtDNA sequences we determine that the species Pharmacus brewsterensis Richards, 1972 is better placed within the genus Notoplectron Richards, 1964. We also resolve the species Isoplectron cochleatum Karny, 1935 and show that it belongs to the genus Pharmacus. Additionally, we describe six new species and three new subspecies from the southern regions of South Island, New Zealand. We provide key traits and known distributions for all known species and subspecies in this alpine genus. New combinations: Pharmacus brewsterensis Richards, 1972 becomes Notoplectron brewsterense (Richards, 1972) comb. nov.; Isoplectron cochleatum Karny, 1935 becomes Pharmacus cochleatus (Karny, 1935) comb. nov. New species and subspecies: Pharmacus cochleatus rawhiti subsp. nov., Pharmacus cochleatus fiordensis subsp. nov., Pharmacus cochleatus nauclerus subsp. nov., Pharmacus concinnus sp. nov., Pharmacus cristatus sp. nov., Pharmacus notabilis sp. nov., Pharmacus perfidus sp. nov., Pharmacus senex sp. nov. and Pharmacus vallestris sp. nov. New synonyms: Pharmacus dumbletoni Richards, 1972 = Pharmacus montanus Pictet & de Saussure, 1893 syn. nov.; Pharmacus chapmanae Richards, 1972 = Pharmacus cochleatus (Karny, 1935) syn. nov

    Diversity and distribution of Pleioplectron Hutton cave wētā (Orthoptera: Rhaphidophoridae: Macropathinae), with the synonymy of Weta Chopard and the description of seven new species

    No full text
    The genus Pleioplectron was first described by Hutton (1896) and included six New Zealand species. This genus has since had three species moved, one each to the genera Pachyrhamma Brunner von Wattenwyl, 1888, Miotopus Hutton, 1898 and Novoplectron Richards, 1958. Here we clarify the status and appearance of Pleioplectron simplex Hutton, 1896 (incl. P. pectinatum Hutton, 1896 syn. nov.) and P. hudsoni Hutton, 1896, as well as P. thomsoni (Chopard, 1923) comb. nov., which is transferred from the genus Weta Chopard, 1923. The genus Weta is newly synonymised with Pleioplectron. We also describe seven new species of Pleioplectron from South Island, New Zealand: P. auratum sp. nov., P. caudatum sp. nov, P. crystallae sp. nov., P. flavicorne sp. nov., P. gubernator sp. nov., P. rodmorrisi sp. nov and P. triquetrum sp. nov. We base these descriptions on morphology using fresh specimens of both male and female adults, and provide support for each with DNA sequence variation (mtDNA, partial COI)

    Relationships among body size components of three flightless New Zealand grasshopper species (Orthoptera, Acrididae) and their ecological applications

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    Body size is perhaps the most fundamental property of an organism and is central to ecology at multiple scales, yet obtaining accurate estimates of ecologically meaningful size metrics, such as body mass, is often impractical. Allometric scaling and mass-to-mass relationships have been used as alternative approaches to model the expected body mass of many species. However, models for predicting body size in key herbivorous insects, such as grasshoppers, exist only at the family level. To address this data gap, we collected empirical body size data (hind femur length and width, pronotum length, live fresh mass, ethanol-preserved mass, and dry mass) from 368 adult grasshoppers of three flightless species at Hamilton Peak, Southern Alps, New Zealand. We examined the relationships among body size components across all species using linear and non-linear regression models. Femur length and preserved mass were robust predictors of both fresh mass and dry mass across all species; however, regressions using preserved mass as a predictor always showed higher predictive power than those using femur length. Based on our results, we developed species-specific statistical linear mixed-effects models to estimate the fresh and dry masses of individual grasshoppers from their preserved mass and femur length. Including sex as an additional co-variate increased model fit in some cases but did not produce better estimates than traditional mass-to-mass and allometric scaling regressions. Overall, our results showed that two easy-to-measure, unambiguous, highly repeatable, and non-destructive size measures (i.e., preserved mass and femur length) can predict, to an informative level of accuracy, fresh and dry body mass across three flightless grasshopper species. Knowledge about the relationships between body dimensions and body mass estimates in these grasshoppers has several important ecological applications, which are discussed
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