Molecular systematics, morphological analysis, and hybrid crossing identify a third taxon, Aedes (Halaedes) wardangensis sp.nov., of the Aedes (Halaedes) australis species-group (Diptera: Culicidae)

1998 ◽  
Vol 76 (7) ◽  
pp. 1236-1246 ◽  
Author(s):  
Reinhart A Brust ◽  
J William O. Ballard ◽  
Felice Driver ◽  
Diana M Hartley ◽  
Nora J Galway ◽  
...  

Phylogenetic and morphological analyses, male morphology, and hybrid crossing indicate that a population from Wardang Island, South Australia, is distinct from the monophyletic series of populations of Aedes (Halaedes) australis (Erichson) 1842 from Victoria, Tasmania, New South Wales, and New Zealand. The name Aedes (Halaedes) wardangensis has been assigned to the new species. Phylogenetic analysis of DNA sequences from the cytochrome oxidase II and internal transcribed spacer loci support the resurrection of Aedes (Halaedes) ashworthi Edwards, 1921 (Brust and Mahon, 1997). Aedes ashworthi is known only from Western Australia and was found to be infertile when crossed with Ae. wardangensis from South Australia and Ae. australis from New Zealand. The hybrid of Ae. australis from New South Wales × Ae. australis from New Zealand was fertile for three generations, documenting these as conspecific.

Author(s):  
D. W. Minter

Abstract A description is provided for Podospora excentrica. Some information on its associated organisms and substrata, dispersal and transmission, habitats and conservation status is given, along with details of its geographical distribution (South America (Venezuela), Atlantic Ocean (Portugal (Madeira)), Australasia (Australia (New South Wales, South Australia, Victoria, Western Australia)), New Zealand, Europe (Belgium, Denmark, Germany, Ireland, Italy, Netherlands, Spain, Sweden, UK)).


2018 ◽  
Vol 50 (5) ◽  
pp. 571-582
Author(s):  
G. KANTVILAS ◽  
E. RIVAS PLATA ◽  
R. LüCKING

AbstractThe genus Coenogonium Ehrenb. in Tasmania comprises seven species. New to science are: C. atherospermatis Kantvilas, Rivas Plata & Lücking, endemic to Tasmania and characterized by pale yellowish beige apothecia and relatively small ascospores, 6–8·5×2·5–3 µm; C. urceolatum Kantvilas, Rivas Plata & Lücking, likewise endemic to Tasmania and characterized by orange, urceolate apothecia, 0·3–0·4 mm wide, and uniseriate ascospores, 8·5–11×2·5–3 µm; and C. australiense Kantvilas & Lücking, recorded from Tasmania, South Australia and New South Wales, and characterized by orange apothecia, 0·5–2 mm wide, and relatively broad ascospores, 10–14×3–4·5 µm. Also treated are C. lutescens (Vĕzda & Malcolm) Malcolm (Tasmania and New Zealand) and three widespread taxa, namely C. implexum Nyl. (Southern Hemisphere), C. luteum (Dicks.) Kalb & Lücking and C. pineti (Schrad. ex Ach.) Lücking & Lumbsch (both subcosmopolitan). All species are described in full from Tasmanian collections and illustrated, and their ecology, variation and affinities to related species are discussed. The Tasmanian taxa are also discussed in the context of the Australasian lichen biota.


1970 ◽  
Vol 12 (3) ◽  
Author(s):  
Lee Richardson

Historians who have asked "why it was the Australasian colonies opted to introduce a compulsory element into their dispute solving mechanisms have given broadly similar answer. Compulsion resulted from the conjunction of a particular stage of union development, a heightened predisposition towards what might be called liberal rationality or a belief in the possibility of resolving clashes of interest by negotiation. Commonly enough historians have also tended to concentrate upon the leadership or sponsorship of a particular individual. Thus the persistent advocacy of William Pember Reeves in New Zealand, C C Kingston in South Australia and B R Wise in New South Wales is often seen as critical to winning acceptance for the legislation. There is much to commend this general explanation for the adoption of a compulsory system of arbitration through out Australasia. It is an historical framework which Jim Holts Compulsory' arbitration in New Zealand endorses. It is when he turns to examine the evolution of the system that he widens our perspective. He stresses the subtle interplay between employers and unions, politicians and administrators and the Arbitration Court itself as each sought to respond to changing circumstances.


2013 ◽  
Vol 41 (2) ◽  
pp. 265-298
Author(s):  
Peter Congdon

Constitutional systems of Westminster heritage are increasingly moving towards fixed-term parliaments to, amongst other things, prevent the Premier or Prime Minister opportunistically calling a ‘snap election’. Amongst the Australian states, qualified fixed-term parliaments currently exist in New South Wales, South Australia and Victoria. Queensland, Tasmania and Western Australia have also deliberated over whether to establish similar fixed-term parliaments. However, manner and form provisions in those states' constitutions entrench the Parliament's duration, Governor's Office and dissolution power. In Western Australia and Queensland, unlike Tasmania, such provisions are doubly entrenched. This article considers whether these entrenching provisions present legal obstacles to constitutional amendments establishing fixed-term parliaments in those two states. This involves examining whether laws fixing parliamentary terms fall within section 6 of the Australia Acts 1986 (Cth) & (UK). The article concludes by examining recent amendments to the Electoral Act 1907 (WA) designed to enable fixed election dates in Western Australia without requiring a successful referendum.


1957 ◽  
Vol 8 (1) ◽  
pp. 29 ◽  
Author(s):  
M Blackburn

The diet of surface-swimming Australian barracouta was studied from over 10,000 stomachs. The principal prey organisms in Bass Strait are the euphausiid Nyctiphanes australis Sars, the anchovy Engraulis australis (White), and young barracouta, in that order; and in eastern Tasmania Nyctiphanes, Engraulis, and the sprat Clupea bassensis McCulloch, in that order. The pilchard Sardinops neopilchardus (Steindachner) is not an important item of the diet in these regions although it is so in New South Wales, South Australia, and Western Australia. The jack mackerel Trachurus declivis Jenyns is a significant item in eastern Tasmania and New South Wales but not in Bass Strait. These and other features of the fish diet of the barracouta reflect actual availability of the various small fish species in the waters. Barracouta eat Nyctiphanes by herding them into dense masses (or finding them already concentrated) and swallowing them. The movements of the anchovy make it unavailable to Bass Strait and eastern Tasmanian barracouta for much of the summer and autumn period, when the barracouta are thus dependent upon Nyctiphanes for the bulk of their food. A close positive relationship between the availability of barracouta and Nyctiphanes might therefore be expected at those seasons. There is evidence of such a relationship between mean availability (catch per boat-month) of barracouta and mean percentage of barracouta stomachs containing Nyctiphanes, at those seasons, from year to year. For southern Victorian coastal waters both show a downward trend from 1948-49 to 1950-51 and then an upward trend to 1953-54; for eastern Tasmania both show a downward trend (for autumn only) from 1949-50 through 1952-53. The records of catch per boat-month furnish independent evidence that the main variations in this index were effects of availability (population distribution or behaviour) rather than abundance (population size), at least for southern Victoria. It is therefore considered that when scarcity of barracouta occurs in summer and autumn in the coastal fishing areas it may be due to scarcity of Nyctiphanes, forcing the fish to go offshore for this food which is known to be available there. This would take the fish out of range of the fishermen.


Author(s):  

Abstract A new distribution map is provided for Monilochaetes infuscans Halsted ex Harter. Hosts: Sweet potato (Ipomoea batatas). Information is given on the geographical distribution in Africa, Sierra Leone, Zimbabwe, Asia, China, Israel, Japan, Korea, Taiwan, Australasia & Oceania, Australia, New South Wales, Queensland, South Australia, Hawaii, New Zealand, US Trust Terr., Europe, Portugal, Azores, North America, USA, South America, Argentina, Brazil.


Author(s):  

Abstract A new distribution map is provided for Pseudomonas syringae pv. pisi (Sackett) Young, Dye & Wilkie. Hosts: Pea (Pisum sativum) and other Apiaceae. Information is given on the geographical distribution in Africa, Kenya, Malawi, Morocco, South Africa, Tanzania, Zimbabwe, Asia, India, Rajasthan, Himachal Pradesh, Indonesia, Israel, Japan, Lebanon, Nepal, Pakistan, Russia, Armenia, Kirghizistan, Australasia & Oceania, Australia, New South Wales, South Australia, Western Australia, Queensland, Tasmania, Victoria, New Zealand, Europe, Bulgaria, Denmark, France, Germany, Greece, Hungary, Italy, Netherlands, Romania, Russia, Ukraine, Voronezh, Moldavia, Switzerland, UK, England, Yugoslavia, North America, Bermuda, Canada, Alberta, British Columbia, Manitoba, Ontario, Quebec, Saskatchewan, Mexico, USA, New York, South America, Argentina, Colombia, Uruguay.


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