A new Candonopsini (Ostracoda) genus from subterranean waters of New South Wales (Australia)

Zootaxa ◽  
2018 ◽  
Vol 4379 (2) ◽  
pp. 247 ◽  
Author(s):  
IVANA KARANOVIC

The Australian Candonidae ostracod fauna has few surface water representatives, despite Australia being one of the principal centers of Candonidae biodiversity. The majority of Australian species live in subterranean waters, with most genera and one tribe being endemic to the continent. Species in Australia show Tethyan and Gondwana connections, with relatives living in European and Central/South American subterranean waters. I describe Hancockcandonopsis gen. nov. from boreholes in the alluvial aquifers of the Peel River and Hunter Valley, which at present contains five species, of which three are named, H. inachos sp. nov., H. io sp. nov., and H. tamworthi sp. nov., and two are left on the open nomenclature. All species are allopatric and short range endemics. The genus belongs to the almost cosmopolitan Candonopsini tribe, and the major generic autapomorphy is a hook-shaped h3-seta on the cleaning leg. Characters on the prehensile palps and hemipenis of Hancockcandonopsis indicate a close relationship with the Queensland genus Pioneercandonopsis Karanovic, 2005 and two West Indies genera, Cubacandona Danielopol, 1978 and Caribecandona Broodbaker, 1983. A cladistic analysis, based on 32 Candonopsini species and 24 morphological characters, is used to test phylogenetic relationships among Candonopsini genera globally. Several hypotheses about the historical biogeography of this tribe are discussed. 

2017 ◽  
Vol 49 (1) ◽  
pp. 1-22 ◽  
Author(s):  
Diego J. Inclán ◽  
James E. O’Hara ◽  
John O. Stireman III ◽  
Hiroshi Shima ◽  
Jaakko Pohjoismäki ◽  
...  

The Glaurocarini are a small Old World tribe of tachinids belonging to the subfamily Tachininae. Two genera are currently recognized, Glaurocara Thomson with 16 species and Semisuturia Malloch with eight species. In this study we describe Semisuturia moffattensis Inclán, O’Hara, Stireman & Cerretti sp. n. from Queensland and New South Wales and compare it with congeners as well as other glaurocarines. The new species is readily identifiable among world glaurocarines by having a row of setae on lower 2/3 of facial ridge. We further evaluate the monophyly of the Glaurocarini on the basis of morphological characters of both adult and larval stages. A molecular phylogenetic analysis also supports monophyly of the tribe but does not support a close relationship between Glaurocarini and Ormiini as has been suggested previously. Finally, we provide new morphological evidence from both adults and first instar larvae to support the monophyly of both Semisuturia and Glaurocara.


2021 ◽  
Vol 53 (1) ◽  
pp. 95-101
Author(s):  
Gintaras Kantvilas

AbstractThe lichen genus Lecanactis Körb. in Tasmania comprises six species: L. abietina (Ach.) Körb., which is widespread and pan-temperate; L. latispora Egea & Torrente and L. neozelandica Egea & Torrente, both shared with New Zealand and with the former recorded here from the Auckland Islands for the first time; L. mollis (Stirt.) Frisch & Ertz, shared with Victoria and New Zealand; L. aff. dilleniana (Ach.) Körb., a European species recorded provisionally for Tasmania on the basis of several sterile collections; L. scopulicola Kantvilas, which is described here as new to science and apparently a Tasmanian endemic. This new taxon occurs in rocky underhangs and is characterized by a thick, leprose thallus containing schizopeltic acid, and 3-septate ascospores, 19–30 × 4.5–6 μm. Short descriptions and a discussion of distribution and ecology are given for all species. A key for all 11 Australian species of the genus is provided, including L. subfarinosa (C. Knight) Hellb. and L. tibelliana Egea & Torrente, which are recorded for Australia for the first time, and L. platygraphoides (Müll.Arg.) Zahlbr., a first record for New South Wales. Lecanactis spermatospora Egea & Torrente and L. sulphurea Egea & Torrente are also included.


Zootaxa ◽  
2017 ◽  
Vol 4362 (2) ◽  
pp. 213 ◽  
Author(s):  
KAI CHEN ◽  
MARIANNE HORAK ◽  
XICUI DU ◽  
DANDAN ZHANG

The genus Agrotera Schrank, 1802 is revised for Australia and the generic definition is refined based on the male genitalia. The genera Leucinodella Strand, 1918 stat. rev. with L. leucostola (Hampson, 1896) comb. nov., Nistra Walker, 1859 stat. rev. with N. coelatalis Walker, 1859 comb. rev., Sagariphora Meyrick, 1894 stat. rev. with S. magnificalis (Hampson, 1893) comb. nov., and Tetracona Meyrick, 1884 stat. rev. with T. amathealis (Walker, 1859) comb. rev. and T. pictalis Warren, 1896 comb. rev. are removed from synonymy with Agrotera, as they lack the synapomorphies of Agrotera. Two new species, Agrotera genuflexa sp. nov. from Northern Territory, Queensland and New South Wales, and A. longitabulata sp. nov. from Queensland, are described. The taxonomic status of the Australian species of Agrotera is discussed, and a key to all species, based on males, is provided. The adults and genitalia of the new species and some related species are figured. 


Author(s):  

Abstract A new distribution map is provided for Pyrenophora tritici-repentis (Died.) Drechsler. Hosts: wheat (Triticum spp.) and other grasses. Information is given on the geographical distribution in AFRICA, Ethiopia, Kenya, Morocco, South Africa, Tanzania, Tunisia, Uganda, ASIA, Afghanistan, Bhutan, China, Zhejiang, India, Bihar, Iran, Israel, Japan, Nepal, Thailand, Turkey, USSR ,: N. Caucasus, AUSTRALASIA & OCEANIA, Australia ,: New South Wales, EUROPE, Austria, Belgium, Cyprus, Czechoslovakia, Denmark, Finland, France, Germany, Hungary, Italy, Latvia, Poland, Romania, Spain, Sweden, Switzerland, UK, England, USSR, Byelorussia, NORTH AMERICA, Canada, Mexico, USA, CENTRAL AMERICA & WEST INDIES, Puerto Rico, SOUTH AMERICA, Bolivia, Brazil, Chile, Colombia, Ecuador, Peru.


Author(s):  

Abstract A new distribution map is provided for Alternaria zinniae M.B. Ellis. Hosts: Zinnia and other Compositae. Information is given on the geographical distribution in AFRICA, Egypt, Ethiopia, Ghana, Guinea, Kenya, Libya, Malawi, Mauritius, Sierra Leone, South Africa, Sudan, Tanzania, Uganda, Zambia, Zimbabwe, ASIA, Brunei, China, India, Uttar Pradesh, MP, Bihar, Delhi, Karnataka, Maharastra, TN, Indonesia, Borneo, Japan, Korea: Republic, Malaysia, Sabah, Nepal, Pakistan, AUSTRALASIA & OCEANIA, Australia, New South Wales, Queensland, Hawaii, Honolulu, New Caledonia, New Zealand, EUROPE, Austria, Bulgaria, Cyprus, Denmark, France, Germany, Hungary, Italy, Netherlands, Norway, Poland, Portugal, Romania, Switzerland, UK, England, Yugoslavia, NORTH AMERICA, Bermuda, Canada, USA, CENTRAL AMERICA & WEST INDIES, Jamaica, SOUTH AMERICA, Brazil.


Author(s):  

Abstract A new distribution map is provided for Verticillium theobromae (Turc.) Mason & Hughes. Hosts: on Banana (Musa). Information is given on the geographical distribution in AFRICA, Angola, Cameroon, Canary Islands, Cape Verde Islands, Egypt, Ethiopia, Ghana, Kenya, Libya, Mauritius, Morocco, Mozambique, Nigeria, Rhodesia, Sierra Leone, Somalia, South Africa, Tanzania, Uganda, Zambia, ASIA, India (MP), Iran, Israel, Lebanon, Thailand, Yemen, AUSTRALASIA & OCEANIA, Australia (Queensland, New South Wales), Fiji, EUROPE, Azores, Cyprus, Greece (Crete), Italy, NORTH AMERICA, Bermuda, CENTRAL AMERICA & WEST INDIES, Cayman Islands, Cuba, Dominica, French, Antilles, Grenada, Haiti, Honduras, Jamaica, Panama, Puerto Rico, St. Lucia, St. Vincent, Trinidad, SOUTH AMERICA, Brazil (San Paulo, Minas Gerais, Espirito Santo), Bolivia, Colombia, Guyana, Peru, Venezuela.


Author(s):  

Abstract A new distribution map is provided for Mycosphaerella berkeleyi Jenkins. Hosts: Groundnut (Arachis hypogaea). Information is given on the geographical distribution in AFRICA, Angola, Cameroon, Chad, Congo, Dahomey, Egypt, Ethiopia, Gambia, Ghana, Guinea, Ivory Coast, Kenya, Libya, Malagasy Republic, Malawi, Mauritius, Morocco, Mozambique, Niger, Nigeria, Rhodesia, Senegal, Sierra Leone, Somalia, South Africa, Sudan, Tanzania, Togo, Uganda, Zaire, Zambia, ASIA, Afghanistan, Bangladesh, Brunei, Burma, Cambodia, China, Hong Kong, India (general), Indonesia (Java), Iran, Iraq, Israel, Japan, Korea, Laos, Peninsular Malaysia (Sabah, Sarawak), Nepal, Pakistan, Philippines, Sri Lanka, Taiwan, Thailand, Timor, Turkey, USSR (Republic of Georgia), Vietnam, AUSTRALASIA & OCEANIA, Australia (New South Wales, Qd), British Solomon Islands, Fiji, Guam, Hawaii, New Caledonia, Papua New Guinea, Tahiti, Tonga, West Irian, EUROPE, Greece, Spain, NORTH AMERICA, Bermuda, Mexico, USA, CENTRAL AMERICA & WEST INDIES, Antilles, Barbados, Cuba, Dominican Republic, Guatemala, Haiti, Honduras, Jamaica, Nicaragua, Panama, Puerto Rico, Salvador, St. Vincent, Trinidad & Tobago, SOUTH AMERICA, Argentina (Cordoba), Brazil (Rio Grande do Sul), Colombia, Guyana, Paraguay, Peru, Surinam, Uruguay, Venezuela.


Author(s):  

Abstract A new distribution map is provided for Botrytis allii Munn. Hosts: Onion (Allium cepa), leek (Allium porrum), shallot (Allium ascalonicum). Information is given on the geographical distribution in Africa, Canary islands, Egypt, Kenya, Morocco, South Africa, Tanzania, Zambia, Asia, Afghanistan, China, Henan, Cyprus, Iran, Iraq, Israel, Japan, Jordan, Korea, Nepal, Pakistan, Saudi Arabia, Taiwan, Vietnam, Australasia & Oceania, Australia, New South Wales, South Australia, Western Australia, Tasmania, Victoria, New Zealand, Europe, Austria, Belgium, Bulgaria, Denmark, Finland, France, Germany, Italy, Netherlands, Norway, Poland, Romania, UK, USSR, Yugoslavia, North America, Canada, Alberta, British Columbia, Manitoba, Ontario, Prince Edward Island, Quebec, Saskatchewan, Mexico, USA, Central America & West Indies, Costa Rica, Guatemala, Jamaica, Panama, Salavador, South America, Brazil, Chile, Venezuela.


Author(s):  

Abstract A new distribution map is provided for Colletotrichum coccodes (Wallr.) Hughes. Hosts: Potato (Solanum tuberosum), tomato (Lycopersicon esculentum). Information is given on the geographical distribution in Africa, Ethiopia, Kenya, Morocco, Nigeria, South Africa, Sudan, Tanzania, Uganda, Zimbabwe, Asia, Afghanistan, Brunei, Burma, China, India, Bihar, Uttar Pradesh, Indonesia, Java, Iran, Israel, Japan, Jordan, Korea, Lebanon, Malaysia, Sabah, Pakistan, Syria, Turkey, USSR, Caucasus, Australasia & Oceania, Australia, Queensland, New South Wales, South Australia, Western Australia, Victoria, Tasmania, New Zealand, Europe, Austria, Belgium, Britain & Northern Ireland, Channel Islands, Bulgaria, Cyprus, Czechoslovakia, Denmark, France, Germany, Greece, Hungary, Irish Republic, Italy, Netherlands, Poland, Portugal, Azores, Romania, Spain, Sweden, Switzerland, USSR, Estonia, Lithuania, Byelorussia, Leningrad, Yugoslavia, North America, Bermuda, Canada, Alberta, Manitoba, New Brunswick, Nova Scotia, Prince Edward Island, Quebec, Saskatchewan, Ontario, USA, Central America & West Indies, Barbados, Jamaica, South America, Brazil, Peru, Venezuela.


2021 ◽  
Author(s):  
Ryan P. O'Donnell ◽  
Jeremy J. Bruhl ◽  
Ian R.H. Telford ◽  
Trevor C. Wilson ◽  
Heidi C. Zimmer ◽  
...  

Research into the systematics of Prostanthera has recently revealed a close evolutionary relationship among P. phylicifolia s. str., the critically endangered P. gilesii, and a population of uncertain identity from the Central Tablelands of New South Wales, Australia. Previous analyses were unable to establish whether genetic boundaries separated these taxa. This study aimed to assess the species boundaries among these three taxa using a combination of single-nucleotide polymorphisms (SNP) sampled at the population-scale and multivariate analysis of morphological characters. Non-parametric and parametric statistics, neighbour-network analysis, phylogenetic analysis, and ancestry coefficient estimates all provided support for discrete genetic differences between the three taxa. Morphological phenetic analysis identified a suite of characters that distinguished each of these taxa. This corroboration of evidence supports the presence of three independently evolving lineages. Prostanthera gilesii and P. phylicifolia s. str. are distinct species independent from the third taxon which is described here as P. volucris R.P.O'Donnell. A detailed description, diagnostic line drawings and photographs are provided. We evaluate P. volucris as satisfying criteria to be considered Critically Endangered.


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