Restriction Analysis of Mitochondrial DNA from the Yellow-footed Rock-wallaby, Petrogale xanthopus: Implications for Management

1997 ◽  
Vol 24 (3) ◽  
pp. 289 ◽  
Author(s):  
M. D. B. Eldridge

The extent of mitochondrial DNA divergence between populations of the vulnerable yellow-footed rock- wallaby, Petrogale xanthopus, was assessed by restriction analysis. Of the 15 restriction endonucleases, five were informative, with a single unique haplotype identified in P. x. celeris from Queensland (Qld) (n = 8) and a further two unique haplotypes in three sampled populations of P. x. xanthopus from New South Wales (NSW) (n = 1) and South Australia (SA) (n = 9). The two subspecies of P. xanthopus were found to be genetically distinct (average sequence divergence = 0·72%). As this divergence is greater than that found between some Petrogale species, it is recommended that populations of P. x. xanthopus and P. x. celeris be managed independently both in captivity and the wild. The NSW population of P. x. xanthopus appears genetically similar to those in SA, although these data are limited.

2006 ◽  
Vol 28 (1) ◽  
pp. 65 ◽  
Author(s):  
J. K. Ling ◽  
C. Atkin ◽  
A. Barnes ◽  
A. Fischer ◽  
M. Guy ◽  
...  

Australian sea lions (Neophoca cinerea) are known to have been kept in aquaria and zoos in Australia since 1965. During that time at least 41 births were recorded, of which 19 were in Adelaide, 15 at Adelaide Zoo and 4 at Marineland of South Australia. The mean interval between successive births in Adelaide was 538.9 � 9.5 days (18.0 months; n = 10) and the mean assumed pregnancy period, including embryonic diapause, was 536.0 � 11.4 days (17.9 months; n = 9). The mean interval between parturition and presumed successful mating was 8.4 � 1.6 days (n = 5). Births occurred in all months except January, June, August and December. Figures for New South Wales and Queensland establishments are too small and scattered over time for any pregnancy periods or birth intervals to be determined. Likewise, latitudinal differences, if any, were not evident, because of the paucity of data from these more northerly places. One female at the Adelaide Zoo produced 8 pups between 1986 and 1997; she is still alive after 22 years in captivity. The youngest known-age (captive-born) female was 4 years, 8 months old when she gave birth to her first pup; and the oldest female in captivity to give birth to a pup was aged approximately 21 years, 8 months. The longest recorded captive period for a female was more than 25 years by 31 December 2003, and for a male it was 21 years, 11 months. A captive-bred female was still alive after 18 years, 2 months, 24 days; another such female died aged 18 years, 2 months, 18 days. These life spans appear to be similar to those that meagre data suggest for tagged N. cinerea in the wild.


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 Mycosphaerella linicola Naumov. Hosts: Flax (Linum usitatissimum) and other (Linum) spp. Information is given on the geographical distribution in Argentina, Australia, New South Wales, Queensland, South Australia, Victoria, Western Australia, Austria, Belarus, Belgium, Brazil, Rio Grande do Sul, Bulgaria, Canada, Alberta, British Columbia, Manitoba, Ontario, Saskatchewan, China, Croatia, Czech Republic, Denmark, Ethiopia, France, Germany, Greece, Hungary, Ireland, Italy, Kazakhstan, Kenya, Mexico, Morocco, New Zealand, Peru, Poland, Portugal, Romania, Russia, Russia (European), Russian Far East, Slovakia, Slovenia, Sweden, Tanzania, Tunisia, Turkey, UK, Scotland, USA, Arizona, California, Iowa, Kansas, Michigan, Minnesota, Montana, North Dakota, South Dakota, Texas, Wisconsin, Ukraine, Uruguay, Yugoslavia (former).


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.


Author(s):  

Abstract A new distribution map is provided for Dacus tryoni[Bactrocera tryoni] (Frogg.) (Dipt., Trypetidae) (Queensland Fruit-fly) Hosts: Many deciduous and subtropical fruits. Information is given on the geographical distribution in AUSTRALIA, New South Wales, Queensland, South Australia, Victoria.


Author(s):  

Abstract A new distribution map is provided for Listronotus bonariensis (Kuschel) Coleoptera: Curculionidae Attacks Lolium spp. and other pasture grasses and cereals. Information is given on the geographical distribution in SOUTH AMERICA, Argentina, Bolivia, Brazil, Chile, Uruguay, OCEANIA, Australia, New South Wales, South Australia, Tasmania, Victoria, Western Australia, New Zealand.


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)).


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