The pseudoscorpions of New Zealand,Norfolk, and Lord Howe

Nearly 20 000 specimens of pseudoscorpions from a full range of habitats have been examined. For New Zealand, 70 species and subspecies in 28 genera are recognised, and for Norfolk and Lord Howe Islands, 11 species in 9 genera. Endemism is very high in this area: in New Zealand, 13 out of 25 indigenous genera are endemic; 2 others (Apatochernes, Nesochernes) are shared with Norfolk Island; and 4 (Sathrochthonius, Austrochthonius, Synsphyronus, Protochelifer) extend their distribution to Australia (Austrochthonius is known also from South America and South Africa). The rest of the native genera have a wider distribution in the Pacific. Three species (Lamprochernes savignyi, Withius subruber, Chelifer cancroides) have a wide and disjunct distribution induced by human traffic, and are considered to be an introduced element.     

The Powelliphanta gilliesi — traversi — hochstetteri — rossiana — lignaria — superba ring species (Mollusca: Pulmonata)

Abstract

An alternative classification of the New Zealand rhytidid genus Powelliphanta O'Connor, 1945 is presented. P. gilliesi (Smith, 1880) and P. hochstetteri (Pfeiffer, 1862) are recognised as species, and the following subspecies are recognised within hochstetteri: h. superba (Powell, 1930); h. lignaria (Hutton, 1880); h. rossiana (Powell, 1930); h. fiordlandica (Climo, 1971). A model is explained which suggests that all described species and subspecies of Powelliphanta are part of a complex ring species. This developed as a result of glacial disjunction of South Island populations and hybridisation across a Cook Strait land bridge formed during the last Pleistocene glaciation.     

Distribution,origin and speciation,wing development,and host‐plant relationships of New Zealand Targaremini (Hemiptera: Lygaeidae)

Three faunal areas—northern (Three Kings Islands, Northland, Auckland, Coromandel Peninsula, and offshore islands), central (most of Nelson, north‐east Buller, Marlborough, Marlborough Sounds, Kaikoura, northern North Canterbury), and southern (Fiordland, southern Otago Lakes, southern Central Otago, southern Dunedin, Southland, Stewart Island) —are each characterised by the local endemicity of about 20% of the total targaremine species of New Zealand. They are separated by areas of no endemicity. Arbitrary subareas are delineated in the northern and southern areas. Species not endemic to a single faunal area have wider ranges covering more than one area. The targaremine faunal areas and subareas are compared with those recognised for other units of the New Zealand biota. Instances of allopatric and parapatric species are listed. All 30 targaremine species in New Zealand are endemic; the effects of Pleistocene cold climate on their distribution and speciation are discussed. Wing development is discussed in relation to its role in initial distribution and dispersal over geographical barriers, and in subsequent adaptations to ecological niches and/or post‐Pleistocene extensions of range. Analysis of host‐plant data reveals that the Targaremini have no marked host specificity; ecologically significant data are presented for several species.     

Polytrichum commune Hedw. and Polytrichadelphus magellanicus (Hedw.) Mitt. used as decorative material on New Zealand Maori cloaks

Abstract

Confirmation of the occurrence of the moss Ptychomnion densifolium on the main islands of New Zealand is provided and the features which separate it from the more common P. aciculare are outlined. A brief account of the history of P. densifolium in New Zealand is given and its morphology there is discussed. A key to the two species in New Zealand is provided and habitat differences between them outlined. New Zealand material differs from type locality (Tristan d' Acunha) material in having longer and more twisted acumens, and in this respect is similar to New Zealand material of P. aciculare. New Zealand populations of P. densifolium are recognisable in having stem leaves reflexed from an oblong sheathing base, and well developed basal leaf plications. It is a relatively widespread species in New Zealand, occurring in mostly upper elevation, open sites.     

Some osteological differences between the blennioid fishes Limnichthys polyactis and L. rendahli,with comments on other species of Creediidae

Abstract

The two endemic species of New Zealand Limnichthys differ in several osteological characters. L. polyactis differs from L. rendahli in having a rayed dorsal margin of the opercle (cf. entire), little or no gap between the lower limb of the coracoid and the pelvis (cf. wide gap), one epural (cf. two), and narrow posterior neural and haemal spines (cf. wide spines). Comments are given on some characters in the other 10 recognised named species of Creediidae. Squamicreedia obtusa is removed from the Creediidae, and is provisionally placed in the Percophididae.     

Good morning Gondwana

Summary

Vicariance and dispersion both must be considered as possibilities for the fauna and flora of New Zealand and New Caledonia. Oligocene submersion, promoted by the geologists and several biologists, does not seem to have been total. Refuge stations must have existed in mountains and even in plains in some surrounding areas. From there the relicts must have radiated after the partial submersion. Certain “primitive” Chrysomelidae Eumolpinae (Bohumiljania spp.) are closely related to Patagonian genera. Their case is not unique among the terrestrial organisms of New Caledonia. How to explain the occurrence of Amborella in New Caledonia and of the tuataras in New Zealand, already very probably extinct elsewhere during the Paleogene?     

A synopsis of the New Zealand Anillini (Coleoptera: Carabidae: Bembidiinae), with descriptions of new genera and species

Abstract

Pelodiaetodes n.gen. (type-species P. prominens n.sp.) and Hygranillus n.gen. (type-species H. kuscheli n.sp.) are described, and the following new synonymies are established: Nesamblyops oreobius (Broun, 1893) = N. coriaceus (Broun, 1908); Zeanillus pallidus (Broun, 1884) = Z. marginatus (Broun, 1914). Nine species of New Zealand Anillini are now recognised; they are distributed between five genera.     

Pselaphotumulus,a new genus of pselaphine endemic to New Zealand (Coleoptera: Staphylinidae: Pselaphinae: Pselaphitae)

ABSTRACT

Pselaphotumulus Owens and Carlton, gen. nov., is described as the sixth genus in the tribe Pselaphini known from New Zealand. Three new species are described: Pselaphotumulus aorerei, sp. nov., Pselaphotumulus dubius, sp. nov. and Pselaphotumulus unus, sp. nov.. Three species, Pselaphus cavelli (Broun 1893), Pselaphus oviceps (Broun 1917) and Pselaphus urquharti (Broun 1917) are transferred to Pselaphotumulus, nov. combs. Lectotypes from type series in the New Zealand Broun Collection (Natural History Museum, London) are designated for these three species. Habitus photographs, distributional maps and line drawings of diagnostic characters are provided for each species. A key to species is provided. Searches of museum collections have not yielded representatives outside of New Zealand, suggesting that this is the first endemic genus in the tribe Pselaphini described from the New Zealand’s main islands, specifically, the South Island. Pselaphotumulus species exhibit restricted distribution patterns that approximately coincide with the Pacific/Indo Australian Plate boundary.     

Moss biogeography in the Tasman Sea region

Abstract

Panbiogeographic track analysis is applied to the distribution of several groups of mosses which occur in the New Zealand region. The analysis highlights areas of biogeographic interest (nodes) in the New Zealand region as follows: 1. New Guinea, 2. New Caledonia, 3. New South Wales/Queensland border in Australia, 4. northern New Zealand, 5. Rapa Island, 6. subantarctic New Zealand.

New Zealand is connected to these nodes by the following standard tracks: 1. New Guinea—New South Wales/Queensland border—Tasmania—subantarctic New Zealand, 2. New Guinea—New Caledonia—New Zealand—subantarctic New Zealand, 3. a central Tasman Sea transversal track; New South Wales/Queensland border—New Caledonia. Rapa Island is connected to the Tasman region by northern New Zealand and New Caledonia.     

Accidental importation of a Japanese bat into New Zealand

Abstract

A juvenile female Japanese pipistrelle (Pipistrellus javanicus abramus) wap found dead on 9 December 1981 in Hamilton, New Zealand, in a package of car parts from Japan. This is apparently the first accidental importation of an exotic bat to New Zealand.     

A review of Buccipagoda Ponder, 2010 and descriptions of new species and a new genus (Gastropoda: Neogastropoda: Buccinoidea: Buccinidae)

This revision addresses two Southern Hemisphere genera in the family Buccinidae. Buccipagoda kengrahami (Ponder, 1982) and B. ponderi n. sp. are recognised from off southern Australia and B. achilles n. sp. from off New Zealand. Sagenotriton n. gen. is introduced for S. ajax n. sp. from off New Zealand, and S. bathybius (Bouchet & Warén, 1986) and S. bonaespei (Barnard, 1963) from off South Africa.     

Limnichthys polyactis,a new species of blennioid fish from New Zealand,with notes on the taxonomy and distribution of other Creediidae (including Limnichthyidae)

Abstract

Limnichthys polyactis n.sp., from the North Island of New Zealand, differs from its nearest relative, the more widespread L. rendahli Parrott, in having a shorter preanal distance (the origin of the anal fin precedes the origin of the dorsal fin, as in the other four species of Limnichthys), fewer cirri along the lower jaw, a shorter snout, and fewer vertebrae. The deepest known occurrence of L. polyactis is 6 m, compared to at least 165 m for L. rendahli. It is suggested that the families Creediidae and Limnichthyidae be combined, the former name having precedence. Notes are given on the taxonomy and distribution of the 13 recognised species, and characters for their separation are keyed.     

New Zealand tectonostratigraphic terranes and panbiogeography

Abstract

Tectonostratigraphic terranes of New Zealand, grouped for purposes of the present discussion into six groups, are briefly reviewed as to their role in the biogeographic evolution of the present day biota of New Zealand. Of all the terranes so far recognised, only the Torlesse (Rakaia) terrane is thought to have originated outside the New Zealand region; of the various models proposed to explain its origin and emplacement, only that by McKinnon (1983) would allow it to have acted as a “raft” that could have transported a biota en masse. The former existence of a “lost continent” (Pacifica), suggested as apossible source for Torlesse sediments, is regarded as improbable. The long time (at least 140 Ma, and probably 190 Ma) since terrane accretion, and the extreme degree of geological (and geographical) complexity and change that New Zealand has undergone since accretion, make it most improbable that the present day distribution of plants and animals among the terranes reflects the original distribution of their ancestors.     

Characterisation (δ13C and δ15N isotopes) of the food webs in a New Zealand stream in the Waitakere Ranges,with emphasis on the trophic level of the endemic frog Leiopelma hochstetteri

Abstract

Leiopelma hochstetteri, the most widespread of New Zealand's native frogs, is recognised as threatened, and is fully protected by legislation. As a first step to characterise the diet and trophic level of L. hochstetteri within streams in the Waitakere Ranges, Auckland, stable carbon and nitrogen isotope analyses were undertaken on a variety of sympatric terrestrial and aquatic plant and animal species, including adult frogs. These results show that: (1) aquatic and terrestrial food webs are linked by terrestrial inputs into the stream; (2) invertebrate and vertebrate predators separate well into distinct trophic groups, and (3) L. hochstetteri occupies an intermediate trophic position among predators, with a diet, at least as an adult, comprising terrestrial invertebrates. Shortfin eels and banded kokopu are identified as potential predators of L. hochstetteri, but data for rats are inconclusive. These results have important implications for the conservation of New Zealand native frog species and riparian stream habitat.     

Leaf hoppers of New Zealand: Subfamilies Aphrodinae,Jassinae, Xestocephalinae,Idiocerinae, and Macropsinae (Homoptera: Cicadellidae)

The cosmopolitan subfamilies Aphrodinae, Jassinae, Xestocephalinae, Idiocerinae, and Macropsinae are diagnosed and the New Zealand species described and illustrated. Each subfamily is represented in New Zealand by only one or two species, those in Idiocerinae having been introduced from Europe or North America. The species Euacanthella brunnea Evans (Aphrodinae) is synonymised with the Australian species E. insularis Evans (new synonymy).     

Protura in native and exotic forests in the North Island of New Zealand

Abstract

This study provides data on population and community ecology of Protura in native forests and Pinus radiata plantations in New Zealand. Abundance, age structure, sex ratios, biodiversity, and relationship with soil chemistry are discussed. Protura were significantly more abundant in pine plantations in comparison to native forests. Among native forests, Protura were most abundant under Southern beech (Nothofagus solandri). The abundance patterns may reflect the association between Protura and fungal communities in the soil. No correlation was found between soil organic matter, nitrogen, phosphorous, pH, cation exchange capacity, and the density of Protura. Protura assemblage composition was significantly related to forest type. New Zealand endemic species were associated with native forests; species with distribution outside New Zealand dominated in pine plantations. The distribution records within New Zealand were expanded for five species. The Protura fauna of New Zealand was increased to 18 species. Berberentulus capensis, Eosentomon australicum and Australentulus tillyardi are new records for New Zealand fauna.     

On the occurrence of Lymnaea auricularia (Gastropoda: Lymnaeidae) in New Zealand

Abstract

The occurrence in New Zealand of Lymnaea auricularia (L.) is recorded for the first time, and its status world-wide is briefly discussed, with particular reference to its role in economic parasitology. The lymnaeid fauna of New Zealand is briefly reviewed.     

Mnioloma fuscum (Marchantiopsida: Calypogeiaceae), an unexpected addition to the indigenous flora of New Zealand

Abstract

Mnioloma fuscum, a liverwort species known to date primarily from tropical-montane regions, is reported for New Zealand for the first time. Its occurrence in New Zealand is unexpected as the next nearest known site is believed to be the Solomon Islands, some 3500 km distant. The occurrence of Mnioloma fuscum in New Zealand highlights the contribution tropical regions have made to the composition of New Zealand's hepatic flora.     

Few genetic differences between Victorian and Western Australian blue penguins,Eudyptula minor

Abstract

Blue penguins, Eudyptula minor, breeding on Penguin Island, Western Australia are considerably larger than other blue penguins in Australia. If genetic isolation is the cause, it may have implications for the conservation status of some blue penguin populations. We compared the sequences of two mitochondrial gene regions (cytochrome‐b and the control region) from Western Australian blue penguins with other populations of blue penguins from Australia and New Zealand. We found few differences between sequences from Western Australia, Phillip Island, Victoria and Otago, New Zealand, although all three differed considerably from other New Zealand blue penguins. Sequences for the control region from the Western Australian blue penguins and 30 more birds breeding at various Australasian sites provided further support for two major clades within Eudyptula; an Australian clade (including Otago) and a New Zealand clade.     

A histochemical study of the swimming musculature of Antarctic fish

The kiore, once common throughout New Zealand, had disappeared from most of the country by the end of the 19th century, and is now found only on certain offshore islands and in areas of Fiordland where at least one of the three introduced European rodent species is absent. It is usually accepted that the kiore was displaced by ship rats (Rattus r. rattus) and Norway rats (R. norvegicus). However, recent investigations on Stewart Island have revealed kiore, ship rats, and Norway rats living in close association, but in the absence of mice (Mus musculus). In the area studied the kiore seemed to inhabit mainly grassland. Re‐examination of possible reasons for the decline of the kiore strongly suggests that competition from mice has been a major contributing factor. It seems that in New Zealand a niche no longer exists for kiore once mice, ship rats, and Norway rats have all become established.