Refine
Document Type
- Part of Periodical (10)
- Article (4)
Language
- English (14)
Has Fulltext
- yes (14) (remove)
Is part of the Bibliography
- no (14) (remove)
Keywords
- New Zealand (14) (remove)
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.
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).
Glemparon Jaschhof, 2013, a previously monotypic genus confined to Sweden, is shown here to be considerably richer in species, with most species found to occur in the Australasian region. Eighteen new species are described: G. tomelilla sp. nov. (from Sweden); G. aotearoa sp. nov., G. birhojohmi sp. nov., G. cervus sp. nov., G. didhami sp. nov, G. kaikoura sp. nov., G. nativitas sp. nov., G. orautahi sp. nov., G. otago sp. nov., G. pureora sp. nov., G. rakiura sp. nov., G. rotoiti sp. nov., G. rotoroa sp. nov., G. tewaipounamu sp. nov., G. waipapa sp. nov., G. waipoua sp. nov. (all from New Zealand); G. manuka sp. nov. and G. warra sp. nov. (both from Tasmania, Australia). Glemparon sagittifer Jaschhof, 2013 is redescribed. Genitalic illustrations are provided allowing for the effective identification of all the species known thus far. Morphological data obtained here are used for revising the generic definition. Dicerura Kieffer, 1898 is hypothesized as the sister group to Glemparon. The case of Glemparon is discussed as a perfect example of the fact that our collective ignorance of porricondyline diversity in most parts of the world is a major impediment to a better understanding of the European species.
New Zealand harbours a considerable number of alien plants and animals, and is often used as a model region for studies on factors determining the outcome of introductions. Alien birds have been a particular focus of research attention, especially to understand the effect of propagule pressure, as records exist for the numbers of birds introduced to New Zealand. However, studies have relied on compilations of bird numbers, rather than on primary data. Here, we present a case study of the alien yellowhammer (Emberiza citrinella) introduced from the UK to New Zealand, to demonstrate how recourse to the primary literature highlights significant data gaps and misinterpretations in these compilations. We show that the history of the introduction, establishment and spread of the yellowhammer in New Zealand can be reconstructed with surprising precision, including details of the ships importing yellowhammers, their survival rates on board, the numbers and locations of release, and the development of public perception of the species. We demonstrate that not all birds imported were released, as some died or were re-transported to Australia, and that some birds thought to be introductions were in fact translocations of individuals captured in one region of New Zealand for liberation in another. Our study confirms the potential of precise historical reconstructions that, if done for all species, would address criticisms of historical data in the evidence base for the effect of propagule pressure on establishment success for alien populations.
Three new species of the order Monhysterida are described based on specimens obtained at depths of 8081 and 9177 m in the Kermadec Trench. Thelonema clarki sp. nov. is characterised by a large body size (3230–4461 μm), short cylindrical buccal cavity, gubernaculum without apophyses, and long conico-cylindrical tail. This is the first record of the genus since its original description over two decades ago from the Peru Basin. Metasphaerolaimus constrictus sp. nov. is characterised by a relatively long body (1232–1623 μm), slightly arcuate spicules without gubernaculum, and conico-cylindrical tail with inner cuticle conspicuously thickened immediately anterior to cylindrical portion. Monhystrella kermadecensis sp. nov. is characterised by a circle of papillose outer labial sensillae slightly anterior to the four short cephalic setae, gubernaculum with caudal apophyses, the presence of distinct cuticularised piece along anterior vaginal wall, and a relatively short conical (males) or conico-cylindrical tail (females) with conical, ventrally-curved spinneret. M. kermadecensis sp. nov. can be differentiated from all other species of the genus, and, indeed, the entire family, based on the variable position of the anterior gonad relative to the intestine. The new species is classified within the Monhysteridae, and not the closely-related Xyalidae, based on the small body size, a smooth cuticle, and the presence of six outer labial papillae and only one testis. Further work is required to clarify the placement of M. kermadecensis sp. nov. relative to other monhysterid genera. A tabular key to all ten valid Metasphaerolaimus species is presented.
The genus Bembidion Latreille (Carabidae: Bembidiini) is reviewed for New Zealand. Thirty-six species-group taxa are recognized. Seven species are described as new: Bembidion (Zecillenus) karikari new species, Bembidion (Zecillenus) puponga new species, Bembidion (Zecillenus) tepaki new species, Bembidion (Zecillenus) waimarama new species, Bembidion (Zemetallina) bullerense new species, Bembidion (Zemetallina) mangamuka new species, Bembidion (Zemetallina) waiho new species. The taxonomic status of two species-group taxa is changed (valid names listed after equal sign): Bembidion (Zeactedium) orbiferum giachinoi Toledano, 2005 = Bembidion (Zeactedium) giachinoi Toledano, 2005; Bembidion (Zeperyphodes) nesophilum Broun, 1886 (previously synonymized with Bembidion (Zeperyphodes) callipeplum Bates, 1878) is resurrected from synonymy. A new synonymy is established (valid name listed after equal sign): Bembidion (Ananotaphus) rotundicolle eustictum Bates, 1878 = Bembidion (Ananotaphus) rotundicolle Bates, 1874. A concise review of the taxonomy of all taxa is provided.
Descriptions, identifi cation keys, illustrations of male genitalia, habitus photos, as well a s distributional data and
maps are given. Extensive information on ecology, biology, dispersal power, and collecting techniques is included for each species.
Rhaptothyreus is arguably the most enigmatic nematode taxon due to a combination of unusual morphological features (e.g., large feather-like amphids, vestigial mouth, trophosome, single spicule), unclear phylogenetic relationships (possible affinities with the Enoplida, Mermithida and Benthimermithida) and a distribution restricted to the deep sea. Here I provide the first record of the genus in the Western Pacific Ocean and describe new morphological features of a moulting juvenile. This specimen is characterised by features that differ markedly from those of the adults, the most prominent being the absence of cephalic sensillae and amphids and the presence of a stylet-like structure in the buccal cavity. Similar contrasts in morphology are found between adults and juveniles of the order Benthimermithida, which is characterised by free-living adults and parasitic juveniles.
Other morphological (large body size, presence of trophosome) and distributional characteristics (predominantly deep-sea distribution, juveniles rare / absent in sediments) are also common to both groups. Published records show that Rhaptothyreus is commonly found in oligotrophic environments (e.g., abyssal plain) where organisms bearing symbiotic bacteria are not typically found, which makes the presence of endosymbiotic bacteria inside the trophosome unlikely. These observations are consistent with the existence of a parasitic juvenile life stage in Rhaptothyreus.
We compared Chatham Island endemic species Xanthocnemis tuanuii to its congenerics from the New Zealand South Island: X. zealandica (newly collected specimens)and X. sinclairi (type specimens plus newly collected material). Two independent tests were performed –geometric morphometrics and molecular. Both analyses were consistent in supporting the status of X. tuanuiias a good species. Species differed statistically in the following morphological traits: head (dorsal view), male appendages (dorsal, lateral, posterior and ventral views), thorax (dorsal view), and penis (dorsal and lateral view). In addition to the original diagnostic features (mainly shape of the male superior appendages), a new morphological character is suggested here which reliably distinguishes the species based on the shape of the inferior appendages. There was no statistical support for the species status of X. sinclairi. The only feature re-ported as diagnostic (lower lobe of male superior appendages) was found to be variable and insufficient to warrant the previously proposed taxonomic rank for X. sinclairi. Molecular analysis of specimens showing identical appendages to the X. sinclairi holotype grouped them with X. zealandica specimens. Therefore X. sinclairi is synonymised with X. zealandica.
For the first time Amphipoda have been discovered living in Bryozoa. A new genus and species of the amphipod family Chevaliidae, Bryoconversor tutus gen. et sp. nov. is described from New Zealand at depths of 530–1500 m. The species lives in an inquiline relationship with the cheilostome bryozoan Onchoporoides moseleyi (Calwelliidae), inhabiting an abfrontal basal coelom of the bryozoan beneath the membranous ectocyst (cuticularized epithelium) that conceals and protects the amphipods. The colony is strengthened along all edges by a unique intracoelomic rod of calcium carbonate that is formed within the marginal kenozooids of the colony. The potential benefits and costs to the bryozoan are discussed.
One feature of global geographic variation in avian body sizes is that they are larger on isolated islands than on continental regions. Therefore, this study aims to assess whether there have been changes in body size following successful establishment for seven passerine bird species (blackbird Turdus merula, song thrush T. philomelos, house sparrow Passer domesticus, chaffinch Fringilla coelebs, greenfinch Chloris chloris, goldfinch Carduelis carduelis, yellowhammer Emberiza citrinella) introduced from the continental islands of the UK to the more isolated oceanic landmass of New Zealand in the middle of the nineteenth century. Measures of tarsus length were taken from individuals from contemporary UK and New Zealand populations of these species, and from historical specimens collected around the time that individuals were translocated from the UK to New Zealand. Analysis of Variance was used to test for size differences between contemporary UK and New Zealand populations, and between historical UK and contemporary UK and New Zealand populations. Historical UK populations have longer tarsi, on average, than 12 (7 UK and 5 New Zealand) of the 14 contemporary populations. Significant decreases in tarsus length relative to the historical populations have occurred in the UK for blackbird, chaffinch and greenfinch, and in the New Zealand blackbird population. Contemporary New Zealand house sparrows have significantly longer tarsi, on average, than both historical and contemporary UK populations. Exposure to novel environments may be expected to lead to changes in the morphology and other traits of exotic species, but changes have also occurred in the native range. In fact, contrary to expectations, the most common differences we found were between contemporary and historical UK populations. Consideration of contemporary populations alone would underestimate the true scale of morphological change in these species over time, which may be due to phenotypic plasticity or genetic adaptation to environmental changes experienced by all populations in the last 150 years.