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Two new species of the family Trefusiidae, viz., Trefusia piperata sp. nov. and Trefusialaimus idrisi sp. nov., are described from the crest of the Chatham Rise, Southwest Pacific Ocean (350 m water depth). The present study provides the first species records for this family in the region. Trefusia and Trefusialaimus comprise twenty and three valid species, respectively. A key to males of Trefusia is provided.
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.
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.
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.
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.
A new species of pearlfish, Echiodon prionodon, is described from three specimens. This species is diagnosed by having a serrated margin on the posterior edge of the fangs, expanded thoracic plates on some abdominal vertebrae and ventral swimbladder tunic ridges. This species was only found in coastal waters around the North Island of New Zealand. The diagnosis of Eurypleuron is revised.
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.
The present study describes five new free-living nematode species and provides three new species records of the family Comesomatidae (genera Cervonema Wieser, 1954, Dorylaimopsis Ditlevsen, 1918, Hopperia Vitiello, 1969, and Kenyanema Muthumbi et al., 1997) from the continental margin of New Zealand, Southwest Pacific. Dichotomous identification keys are provided for all known species of Dorylaimopsis and Hopperia. Cervonema shiae Chen & Vincx, 2000 is recorded for the first time outside the type locality (Beagle Channel, Chile). C. kaikouraensis sp. nov. is characterised by amphideal fovea with 5.5 turns situated at 1.7 head diameter from anterior end, jointed outer labial setae, equal in length to cephalic setae, sperm dimorphism, and 5-6 small pre-cloacal supplements. C. multispira sp. nov. is characterised by amphideal fovea with 8.0-8.5 turns situated at 2.6-4.0 head diameter from anterior end, cephalic setae 2-3 μm long, slightly shorter than outer labial setae, presence of six uninucleated cells in males (potentially pseudocoelomocytes or supplementary excretory cells), 5 small pre-cloacal supplements, and strongly cuticularised, arcuate spicules with capitulum. C. proberti sp. nov. is characterised by amphideal fovea with 5 turns and located at < 1 head diameter from anterior end, cephalic setae 1.6-2.0 times longer than outer labial setae, and 8 small pre-cloacal supplements. Dorylaimopsis nodderi sp. nov. is characterised by cuticle with lateral differentiation consisting of three longitudinal rows of larger dots in the pharyngeal and caudal regions, two rows of larger dots in middle region of body, and spicules with rounded ventral projection at one third of spicule length from distal end, giving appearance of a joint. Hopperia ancora sp. nov. is characterised by short conical cephalic setae, spicules with hook-like projection at distal end, gubernaculum with bent apophyses, and 11-13 pre-cloacal supplements. H. beaglense Chen & Vincx, 1998 is recorded from Kaikoura Canyon, the fi rst record of this species outside the type locality (Beagle Channel, Chile). Kenyanema monorchis Muthumbi et al., 1997 is also recorded for the first time outside the type locality (Indian Ocean).
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.