Classification and distribution of Tabanidae (Diptera)

1954 ◽  
Vol 2 (3) ◽  
pp. 431 ◽  
Author(s):  
IM Mackerras
Keyword(s):  
New Zealand ◽  
South America ◽  
Radial Distribution ◽  
Southern Africa ◽  
World Wide ◽  
Primitive Groups ◽  
Early Stages ◽  
The Family ◽  
Southern Regional

The old primary classification of the Tabanidae, based on the presence or absence of hind tibia1 spurs, has been replaced by one based primarily on the genitalia of both sexes, but supported by a significant, though not complete, correlation with external characters. The early stages, so far as known, support the new arrangement. The following subfamilies and tribes are recognized: Pangoniinae Scepsidinae Chrysopinae Tabaninue Pangoniini Bouvieromyiini Diachlorini Scionini Chrysopini Haematopotini Philolichini Rhinomyzini Tabanini Distribution of the family is world-wide, but can be divided into three main sections. More primitive groups are predominantly southern, occurring in some or all of South America, southern Africa, Australia, and New Zealand, with occasional northern extensions, and, in one case (Pangoniini), an extensive Holarctic arc. More specialized groups show two patterns. Southern regional radiations have occurred in South America and Africa, with extensions respectively into the Nearctic and Oriental-Australasian regions. Northern radiation of Chrysopini,Haematopotini, and Tabanini has resulted in a radial distribution like that of the eutherian mammals.

The Cretaceous and Paleocene pleurotomariid (Gastropoda: Vetigastropoda) fauna of Seymour Island, Antarctica

2009 ◽  
Vol 83 (5) ◽  
pp. 750-766 ◽  
Author(s):  
M. G. Harasewych ◽  
Anton Oleinik ◽  
William Zinsmeister
Keyword(s):  
Species Richness ◽  
New Zealand ◽  
South America ◽  
Late Cretaceous ◽  
Upper Cretaceous ◽  
Southern India ◽  
New Combination ◽  
The Family ◽  
The Status ◽  
Seymour Island

Leptomaria antipodensis and Leptomaria hickmanae are described from the Upper Cretaceous [Maastrichtian] Lopez de Bertodano Formation, Seymour Island, and represent the first Mesozoic records of the family Pleurotomariidae from Antarctica. Leptomaria stillwelli, L. seymourensis, Conotomaria sobralensis and C. bayeri, from the Paleocene [Danian], Sobral Formation, Seymour Island, are described as new. Leptomaria larseniana (Wilckens, 1911) new combination, also from the Sobral Formation, is redescribed based on better-preserved material. The limited diversity of the pleurotomariid fauna of Seymour Island is more similar to that of the Late Cretaceous faunas of Australia and New Zealand in terms of the number of genera and species, than to the older, more diverse faunas of South America, southern India, or northwestern Madagascar, supporting the status of the Weddelian Province as a distinct biogeographic unit. The increase in the species richness of this fauna during the Danian may be due to the final fragmentation of Gondwana during this period.

A molecular phylogeny of the circum-Antarctic Opiliones family Neopilionidae

2021 ◽  
Author(s):  
Gonzalo Giribet ◽  
Kate Sheridan ◽  
Caitlin M. Baker ◽  
Christina J. Painting ◽  
Gregory I. Holwell ◽  
...  
Keyword(s):  
New Zealand ◽  
South America ◽  
Morphological Study ◽  
18S Rrna ◽  
New Caledonia ◽  
Sister Group ◽  
28S Rrna ◽  
South American ◽  
Australian Species ◽  
The Family

The Opiliones family Neopilionidae is restricted to the terranes of the former temperate Gondwana: South America, Africa, Australia, New Caledonia and New Zealand. Despite decades of morphological study of this unique fauna, it has been difficult reconciling the classic species of the group (some described over a century ago) with recent cladistic morphological work and previous molecular work. Here we attempted to investigate the pattern and timing of diversification of Neopilionidae by sampling across the distribution range of the family and sequencing three markers commonly used in Sanger-based approaches (18S rRNA, 28S rRNA and cytochrome-c oxidase subunit I). We recovered a well-supported and stable clade including Ballarra (an Australian ballarrine) and the Enantiobuninae from South America, Australia, New Caledonia and New Zealand, but excluding Vibone (a ballarrine from South Africa). We further found a division between West and East Gondwana, with the South American Thrasychirus/Thrasychiroides always being sister group to an Australian–Zealandian (i.e. Australia + New Zealand + New Caledonia) clade. Resolution of the Australian–Zealandian taxa was analysis-dependent, but some analyses found Martensopsalis, from New Caledonia, as the sister group to an Australian–New Zealand clade. Likewise, the species from New Zealand formed a clade in some analyses, but Mangatangi often came out as a separate lineage from the remaining species. However, the Australian taxa never constituted a monophyletic group, with Ballarra always segregating from the remaining Australian species, which in turn constituted 1–3 clades, depending on the analysis. Our results identify several generic inconsistencies, including the possibility of Thrasychiroides nested within Thrasychirus, Forsteropsalis being paraphyletic with respect to Pantopsalis, and multiple lineages of Megalopsalis in Australia. In addition, the New Zealand Megalopsalis need generic reassignment: Megalopsalis triascuta will require its own genus and M. turneri is here transferred to Forsteropsalis, as Forsteropsalis turneri (Marples, 1944), comb. nov.

Corrigendum to: Systematics and distribution of world hyptiogastrine wasps (Hymenoptera : Gasteruptiidae)

2002 ◽  
Vol 16 (6) ◽  
pp. 957 ◽  
Author(s):  
J. T. Jennings ◽  
A. D. Austin
Keyword(s):  
New Species ◽  
New Zealand ◽  
South America ◽  
New Caledonia ◽  
Cladistic Analysis ◽  
Taxonomic Revision ◽  
Morphological Characters ◽  
The Family ◽  
New Hebrides ◽  
New Britain

This study examines the phylogeny, taxonomy, distribution and biology of the gasteruptiid subfamily Hyptiogastrinae and, at the same time, presents an overview of the family. Following a cladistic analysis of 35 discrete morphological characters, two monophyletic genera are recognised, Hyptiogaster Kieffer and Pseudofoenus s. l. Kieffer. As a consequence, the genera Aulacofoenus Kieffer, Crassifoenus Crosskey, and Eufoenus Szépligeti are synonymised with Pseudofoenus. A total of 88 species are recognised for the subfamily, 10 species of Hyptiogaster, which are restricted to mainland Australia, and 78 species of Pseudofoenus, 40 of which are described as new. Pseudofoenus has a restricted Gondwanan distribution and is found in Australia including Tasmania (65 spp.), New Guinea and New Britain (5 spp.), the south-west Pacific (New Caledonia, New Hebrides and Fiji – 2 spp.), New Zealand (4 spp.) and South America (2 spp.). No new species have been recorded from either New Zealand or South America. For Pseudofoenus, information on the distribution of each species, their biology (if known) and an identification key are presented.Following a taxonomic revision, the following new species are described: P. baileyi, sp. nov., P. baitetaensis, sp. nov., P. beverlyae, sp. nov., P. caperatus, sp. nov., P. cardaleae, sp. nov., P. carrabinensis, sp. nov., P. claireae, sp. nov., P. collessi, sp. nov., P. coorowensis, sp. nov., P. crosskeyi, sp. nov., P. douglasorum, sp. nov., P. eliseae, sp. nov., P. ericae, sp. nov., P. eustonensis, sp. nov., P. feckneri, sp. nov., P. gressitti, sp. nov., P. gullanae, sp. nov., P. hackeri, sp. nov., P. imbricatus, sp. nov., P. iqbali, sp. nov., P. kadowi, sp. nov., P. karimuiensis, sp. nov., P. kelleri, sp. nov., P. leinsterensis, sp. nov., P. macdonaldi, sp. nov., P. malkini, sp. nov., P. marshalli, sp. nov., P. masneri, sp. nov., P. mitchellae, sp. nov., P. morganensis, sp. nov., P. nalbarraensis, sp. nov., P. pumilis, sp. nov., P. schmidti, sp. nov., P. stevensi, sp. nov., P. tasmaniensis, sp. nov., P. taylori, sp. nov., P. umboiensis, sp. nov., P. walkeri, sp. nov. and P. zborowskii, sp. nov. The synonymy of Aulacofoenus, Crassifoenus and Eufoenus with Pseudofoenus result in the following new combinations: from Aulacofoenus: P. bungeyi (Jennings & Austin), comb. nov., P. deletangi (Schletterer), comb. nov., P. fallax (Schletterer), comb. nov., P. fletcheri (Jennings & Austin), comb. nov., P. goonooensis (Jennings & Austin), comb. nov., P. infumatus (Schletterer), comb. nov., P. kurmondi (Jennings & Austin), comb. nov., P. loxleyi (Jennings & Austin), comb. nov., P. marionae (Jennings & Austin), comb. nov., P. perenjorii (Jennings & Austin), comb. nov., P. swani (Jennings & Austin), comb. nov., P. thoracicus (Guérin Menéville), comb. nov., P. whiani (Jennings & Austin), comb. nov. and P. wubinensis (Jennings & Austin), comb. nov.; from Crassifoenus: P. houstoni (Jennings & Austin), comb. nov., P. grossitarsis (Kieffer), comb. nov and P. macronyx (Schletterer), comb. nov.; and from Eufoenus: P. antennalis (Schletterer), comb. nov., P. australis (Westwood), comb. nov., P. crassitarsis (Kieffer), comb. nov., P. darwini (Westwood), comb. nov., P. extraneus (Turner), comb. nov., P. ferrugineus (Crosskey), comb. nov., P. floricolus (Turner), comb. nov., P. inaequalis (Turner), comb. nov., P. melanopleurus (Crosskey), comb. nov., P. minimus (Turner), comb. nov., P. nitidiusculus (Turner), comb. nov., P. patellatus (Westwood), comb. nov., P. pilosus (Kieffer), comb. nov., P. reticulatus (Crosskey), comb. nov., P. rieki (Crosskey), comb. nov., P. ritae (Cheesman), comb. nov. and P. spinitarsis (Westwood), comb. nov. Pseudofoenus microcephalus (Crosskey), comb. nov. is transferred from Hyptiogaster and Eufoenus flavinervis (Kieffer) remains incertae sedis.

scholarly journals Studies on the Systematics and Anatomy of New Zealand Earthworms

2021 ◽  
Author(s):  
◽  
Kenneth Ernest Lee
Keyword(s):  
South Africa ◽  
New Zealand ◽  
South America ◽  
Salt Water ◽  
Wide Distribution ◽  
Late Nineteenth Century ◽  
The Family ◽  
America South ◽  
Late Nineteenth ◽  
Original Area

<p>The study of New Zealand earthworms has been extensive, but has been confined principally to the systematics of the group. Only one family of the Oligochaeta, the Megascolecidae, is represented in the endemic fauna, but within this family, over eighty species, belonging to seventeen genera, have been recorded and described. Apart from the Megascolecidae, certain species, lumbricids, worldwide in their distribution, are present and are regarded as having been introduced through the agency of man. The family Megascolecidae is confined almost entirely to the Southern hemisphere, and the southern regions of the Northern hemisphere, and within these regions, the greatest number of species occur in New Zealand, South America, South Africa, and Australia. When the distribution of the Megascolecidae became known, in the late nineteenth century, its sporadic nature evoked a great deal of interest among zoo-geographers, since earthworms, being terrestrial, and unable to tolerate immersion in salt water, form an ideal basis for the consideration of dispersal problems among terrestrial animals as a whole. The interest thus aroused in the Megascolecidae led to much work on the group in New Zealand. Michaelsen (1913 (b)) accounts for the predominance of the Megascolecidae in the southern continental areas by postulating that originally the family had a wide distribution in the nothern and southern continents, and that other families (e.g. the Glossoscolecidae), evolved more recently in the northern continents, have gradually superseded the Megascolecidae in all but the most remote regions of their original area of distribution. Matthew (1915) came to a similar conclusion in regard to the origin of present southern faunas in the course of his work on the distribution and evolution of the Mammalia. Evidence in favour of Michaelsen's conclusions can also be derived from the distribution of slugs, spiders, Collembola, Coleoptera, littoral Echinoderms, Polychaeta and Brachiopoda in the southern land masses.</p>

Tertiary Bryozoan genera in the present-day Australiasian fauna — Implications for classification and biogeography

1994 ◽  
Vol 8 (2) ◽  
pp. 283 ◽  
Author(s):  
DP Gordon
Keyword(s):  
South Africa ◽  
New Zealand ◽  
South America ◽  
Type Species ◽  
Southern South America ◽  
South West ◽  
The Family ◽  
The Mediterranean ◽  
Subjective Synonym

The type species of three little-known Tertiary bryozoan genera have been examined and redescribed. Victorian Bitectipora lineata, previously the only recognised species of Bitectiporidae, is shown to be related to a present-day New Zealand species which may now also be included in Bitectipora. Further, the family Bitectiporidae MacGillivray, 1895 is here considered to be a senior subjective synonym of Hippoporinidae Brown, 1952. Schizosmittina, a French Miocene genus, is confirmed to be congeneric with a suite of Holocene Australasian species and removed from the Smittinidae to the Bitectiporidae. However, on the basis of ovicellular morphology, both families are considered to be closely related. The scarcely used superfamily taxon Smittinoidea is re-established for those families with 'smittinid' ovicells (in contradistinction to 'schizoporellid' ovicells). The genus Stephanollona, based on a French Miocene species, is recognised to be a senior subjective synonym of Brodiella (Phidoloporidae), which includes present-day species from Australasia, South Africa, southern South America, Madeira, south-west Britain and the Mediterranean.

Morphological and taxonomic relationships among branched, ligulate members of the genus Desmarestia (Phaeophyceae, Desmarestiales), with particular reference to South African D. firma

1985 ◽  
Vol 63 (3) ◽  
pp. 437-447 ◽  
Author(s):  
Robert James Anderson
Keyword(s):  
New Zealand ◽  
South America ◽  
South African ◽  
Southern Africa ◽  
Cortical Cells ◽  
Size And Shape ◽  
Signy Island ◽  
Gough Island ◽  
Taxonomic Implications ◽  
Reproductive Anatomy

An examination is made of the reproductive anatomy and the morphology of branched, ligulate members of the genus Desmarestia from worldwide localities. Entities from southern Africa, New Zealand, South America, Gough Island, northwestern America, and Europe show varying degrees of morphological overlap, but all possess sporangia similar in size and shape to, and scattered among, the vegetative cortical cells. Specimens from Signy Island (South Orkneys) have sporangia subtended by stalk cells, interspersed with sterile paraphyses, and arranged in a palisadelike sorus (Antarctic type). The taxonomic implications of these findings are discussed. The New Zealand and Gough entities are referred to D. ligulata (Stackhouse) Lamouroux and the name D. firma (C.Ag.) Skottsb. is retained for the southern African entity.

Four new genera of Mesoveliidae (Hemiptera, Gerromorpha) and the phylogeny and classification of the family

1980 ◽  
Vol 11 (4) ◽  
pp. 369-392 ◽  
Author(s):  
N. Møller Andersen ◽  
John Polhemus
Keyword(s):  
New Zealand ◽  
Type Species ◽  
Habitat Preferences ◽  
New Genera ◽  
Check List ◽  
Aquatic Habitats ◽  
Lava Tubes ◽  
Marine Habitats ◽  
The Family

AbstractCryptovelia terrestris n. gen., n. sp. (Brazil), Darwinivelia fosteri n. gen., n. sp. (Galapagos Is.), Mniovelia kuscheli n. gen., n. sp. (New Zealand), and Cavaticovelia n. gen. (type-species: Speovelia aaa Gagné & Howarth, 1975; Hawaii) are described. The phylogenetic relationships between the mesoveliid genera are discussed in the light of characters revealed by the new taxa. Habitat preferences of mesoveliids include humid terrestrial and/or marginal aquatic habitats, which probably are the most ancestral, and lava-tubes, coastal caves, intertidal marine habitats, and the plant-covered freshwater surface, which probably are the derived kinds of habitats. A classification of the Mesoveliidae with a check list of genera and species is presented. Two subfamilies are recognized: Madeoveliinae (with two genera) and Mesoveliinae (seven genera). The biogeography of the Mesoveliidae is finally discussed.

scholarly journals Studies on the Systematics and Anatomy of New Zealand Earthworms

2021 ◽  
Author(s):  
◽  
Kenneth Ernest Lee
Keyword(s):  
South Africa ◽  
New Zealand ◽  
South America ◽  
Salt Water ◽  
Wide Distribution ◽  
Late Nineteenth Century ◽  
The Family ◽  
America South ◽  
Late Nineteenth ◽  
Original Area

<p>The study of New Zealand earthworms has been extensive, but has been confined principally to the systematics of the group. Only one family of the Oligochaeta, the Megascolecidae, is represented in the endemic fauna, but within this family, over eighty species, belonging to seventeen genera, have been recorded and described. Apart from the Megascolecidae, certain species, lumbricids, worldwide in their distribution, are present and are regarded as having been introduced through the agency of man. The family Megascolecidae is confined almost entirely to the Southern hemisphere, and the southern regions of the Northern hemisphere, and within these regions, the greatest number of species occur in New Zealand, South America, South Africa, and Australia. When the distribution of the Megascolecidae became known, in the late nineteenth century, its sporadic nature evoked a great deal of interest among zoo-geographers, since earthworms, being terrestrial, and unable to tolerate immersion in salt water, form an ideal basis for the consideration of dispersal problems among terrestrial animals as a whole. The interest thus aroused in the Megascolecidae led to much work on the group in New Zealand. Michaelsen (1913 (b)) accounts for the predominance of the Megascolecidae in the southern continental areas by postulating that originally the family had a wide distribution in the nothern and southern continents, and that other families (e.g. the Glossoscolecidae), evolved more recently in the northern continents, have gradually superseded the Megascolecidae in all but the most remote regions of their original area of distribution. Matthew (1915) came to a similar conclusion in regard to the origin of present southern faunas in the course of his work on the distribution and evolution of the Mammalia. Evidence in favour of Michaelsen's conclusions can also be derived from the distribution of slugs, spiders, Collembola, Coleoptera, littoral Echinoderms, Polychaeta and Brachiopoda in the southern land masses.</p>

scholarly journals The plant family Asteraceae: 5. Classification and the subfamily Cichorioideae

2003 ◽  
Vol 22 (1) ◽  
pp. 45-49
Author(s):  
P. P.J. Herman
Keyword(s):  
Southern Africa ◽  
Plant Family ◽  
Flora Of Southern Africa ◽  
The Family

The classification of the plant family Asteraceae is discussed. The family belongs to the division Spermatophyta (Magnoliophyta), subdivision Angiospermae, class Dicotyledoneae (Magnoliopsida), subclass Asteridae, superorder Asteranae and the order Asterales and is divided into three subfamilies: the Barnadesioideae (not in Flora of southern Africa region), the Cichorioideae and the Asteriodeae. The subfamily Cichorioideae is further divided into eight tribes of which one (Liabeae) does not occur in southern Africa and one genus (Corymbium) is not assigned to a tribe. The subfamily Asteriodeae is divided into 10 tribes. The subfamily Cichorioideae and its tribes are more fully described in this article. The genera belonging to these tribes are listed and their distribution given.

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