The Prehistory of South Polynesia

Author(s):  
Atholl Anderson

Southern Polynesia, including New Zealand, the outlying Norfolk, Kermadec, Chatham, and Auckland Island groups was colonized after A.D. 1200 by populations from Central East Polynesia. Interaction between Eastern Polynesian and Southern Polynesian populations ceased soon after colonization, although interaction between the various outlying islands and the New Zealand population continued for possibly another 200 years. Early New Zealand populations exploited plentiful moa, a large flightless bird, and pinnipeds as food sources, hunting the former to extinction. Later horticultural activities, especially in the more clement North Island, focused on kumara or sweet potato. Although Maori society was never as hierarchical as East Polynesian populations, there is abundant archaeological and ethnographic evidence of later complex social and political systems, exchange or distribution networks for utilitarian and prestige goods, and extensive competition between groups, most prominently indicated by the approximately 7,000 fortified sites or pa distributed largely within horticultural landscapes.

2012 ◽  
Vol 19 (4) ◽  
pp. 453-480
Author(s):  
Lee E. Dutter

Studies of individuals or groups who might use violence or terrorism in pursuit of political goals often focus on the specific actions which these individuals or groups have taken and on the policies which defenders (that is, governments of states) against such actions may adopt in response. Typically, less attention is devoted to identifying the relevant preconditions of political action and possible escalation to violence and how or why potential actions may be obviated before they occur. In the context of democratic political systems, the present analysis addresses these issues via examination of indigenous peoples, who typically constitute tiny fractions of the population of the states or regions in which they reside, in terms of their past and present treatment by governments and the political actions, whether non-violent or violent, which individuals from these peoples have engaged or may engage. The specific peoples examined are Aborigines and Torres Strait Islanders of Australia, Haudenosaunee of North America, Inuit of Canada, Maori of New Zealand, and Saami of Scandinavia.


1964 ◽  
Vol 12 (2) ◽  
pp. 282 ◽  
Author(s):  
SI Ali

Reasons for the retention of the name Senecio lautus Forst. f. ex Willd. for both New Zealand and Australian forms are advanced. It is concluded that the New Zealand population should be given the status of a subspecies. Synonymy of S. lautus subsp. lautus and typification of various names involved are discussed. S. glaucophyllus subsp. discoideus (T. Kirk) Ornd. is reported for the first time from Tasmania.


Heart ◽  
2012 ◽  
Vol 98 (23) ◽  
pp. 1728-1731 ◽  
Author(s):  
Prashanthi V Sangu ◽  
Isuru Ranasinghe ◽  
Bernadette Aliprandi Costa ◽  
Gerard Devlin ◽  
John Elliot ◽  
...  

1996 ◽  
Vol 36 (2) ◽  
pp. 109-117 ◽  
Author(s):  
J.F. Hamilton ◽  
L. Starling ◽  
S.J. Cordiner ◽  
D.L. Monahan ◽  
J.S. Buckleton ◽  
...  

2010 ◽  
Vol 63 ◽  
pp. 275-275
Author(s):  
A.J. Puketapu

The tomato/potato psyllid Bactericera cockerelli (Sulc) (Hemiptera Triozidae) is an introduced pest of solanaceous crops in New Zealand A range of established plants play host to Bactericera cockerelli including three traditional Maori food sources taewa or Maori potatoes (Solanum tuberosum ssp andigena) kumara (Ipomoea batatas) and poroporo (Solanum aviculare) Taewa and kumara are highly susceptible to summer B cockerelli infestation whilst poroporo an evergreen plant remains susceptible yearround and provides overwintering refuge Extensive monitoring of each host plant was carried out to determine the significance of each host in the lifecycle of B cockerelli in New Zealand Poroporo was monitored from late autumn for 6 months to determine if the plant served as a significant overwintering host for the pest after harvesting summer crops Taewa and kumara plants were monitored throughout the summer growing season on a weekly basis increasing to twice a week as populations proliferated Host plants were monitored both in the natural environment and under laboratory conditions Data collected contributed to tracking population development of B cockerelli on each host including the length of each life stage (ie egg nymph adult) Comparisons between the three hosts revealed host preference host suitability and the significance of each host in the lifecycle progression of B cockerelli


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