Conflict transition, emplaced identity and the gendered politics of scale in Solomon Islands

2020 ◽  
Vol 55 (4) ◽  
pp. 518-534
Author(s):  
Nicole George

Although there is growing recognition that women’s participation is critical for the durability of peaceful conflict transition, grounded research examining the political scale of women’s participation has not been common. Where feminist researchers have tackled this topic, they have generally reproduced binary representations of political space, sometimes strongly critical of local spaces as restrictive of women, sometimes strongly critical of a hegemonic liberal international. In this article, I address the issue of women’s participation in conflict transition governance from another more ethnographic angle, drawing from fieldwork conducted in the Solomon Islands, a Pacific Islands country destabilised by conflict in the late 1990s and early 2000s. I apply theories of political scale to consider where and how women are politically active in the conflict transition environment, how that political activity is constituted relative to other political scales and where and how women seek to make their political ambitions understood. The ‘emplacement’ lens I develop offers a critical vantage point for analysis of the ways women constitute political identities and the agendas they might meaningfully progress, at scales ranging from the small worlds of the household and the community to the broader scale of national politics.

2013 ◽  
Vol 15 (4) ◽  
pp. 493-527 ◽  
Author(s):  
Anthony J. Nownes ◽  
Nurgul R. Aitalieva

What is the nature and extent of corporate leader involvement in American national politics? The results of a mail survey of nearly 100 such individuals show that leaders are quite active, devoting an average of nearly 1 hour per day to national political activity. We also show that corporate leaders engage in a wide range of advocacy activities. Monetary activities loom particularly large in the political lives of American corporate leaders, as large numbers are approached by members of Congress for contributions, and many who are approached answer the call. In addition, we find that corporate leaders, unlike advocacy professionals, do a great deal of their advocacy work in private; for the most part they eschew public activities such as testifying before congressional committees. Speaking to the question of which leaders are most politically active, our data evince a strong relationship between firm political activity and firm leader political activity. In sum, politically active firms have politically active leaders. We thus contribute to the ongoing academic discussion of corporate political activity by showing that the CEO's office is an additional locus of political power within business firms, and that CEO political activity is instrumental rather than consumptive in nature.


1988 ◽  
Vol 1 (4) ◽  
pp. 11-14
Author(s):  
Ronald J. Oakerson

Occasional references to the old radical teaching that “all politics is local” notwithstanding, American political scientists have by and large treated the study of local politics as a subject of much lesser importance than national politics. The standard introductory course in “American democracy” has a national focus—often it is exclusively national. Briefly, in the late 1960s and early 1970s, the study of “urban politics” occupied a more prominent place in the discipline, but interest has waned. The priority concern in both teaching and research continues to be American national government and politics.This narrow focus leads to a distorted and truncated view of American democracy. Despite increased nationalization, state and local government has been and remains a basic element in the practice of American politics. The productivity and creativity of democracy in America are outcomes, not simply of a national political process, but of a complex system of governance in which local collective action provides much of the energy and initiative for addressing public problems. A vast amount of political activity in the United States is channeled through state and local institutions, where much of the work of public problem solving is done.


Author(s):  

Abstract A new distribution map is provided for Dysdercus sidae Montr. (D. insular is Stål) (Hemipt., Pyrrhocoridae). Host Plants: Cotton, kapok, Hibiscus spp. Information is given on the geographical distribution in AUSTRALASIA AND PACIFIC ISLANDS, Australia, Fiji, Loyalty Islands, New Caledonia, New Hebrides, Niue, Papua & New Guinea, Samoa, Solomon Islands, Tonga, Wallis Islands, Irian Jaya.


Author(s):  

Abstract A new distribution map is provided for Hypsipyla robusta (Moore) (Lep., -Pyrandae) (Toon shoot-and fruit-borer). Host Plants: Cedrella, Khaya, Toona. Information is given on the geographical distribution in ASIA, Andaman Is, Burma, India, Indonesia, Malaysia, Pakistan, Sikkim, Singapore, Sri Lanka, AFRICA, Ghana, Madagascar, Malawi, Mauritius, Nigeria, Sierra Leone, Tanzania, Uganda, AUSTRALASIA, and PACIFIC ISLANDS, Australia, Papua New Guinea, Solomon Islands.


Author(s):  

Abstract A new distribution map is provided for Leptoglossus australis (F.) (=L. membranaceus (F.), L. bidentatus Montr.) (Hemipt, Coreidae) (Leaf-footed Plant Bug). Host Plants: Cucurbits, Citrus and legumes. Information is given on the geographical distribution in ASIA, Andaman Islands, Burma, Cambodia, Ceylon, China, India, Indonesia, Malaysia, Nicobar Islands, Bangladesh, Philippine Islands, Taiwan, Thailand, AFRICA, Angola, Annobon Islands, Botswana, Burundi, Cameroon, Canary Islands, Central African Republic, Chad, Congo, Dahomey, Ethiopia, Ghana, Guinea, Ivory Coast, Kenya, Liberia, Madagascar, Malawi, Mali, Mauritania, Mauritius, Mozambique, Niger, Nigeria, Rhodesia, Rodriguez Islands, Rwanda, Saõ Tomé, Senegal, Seychelle, Sierra Leone, Somalia, Tanzania, Togo, Uganda, Upper Volta, AUSTRALASIA and PACIFIC ISLANDS, Australia, Caroline Islands, Fiji, Mariana Islands, New Caledonia, New Hebrides, Papua & New Guinea, Western Samoa, Society Islands, Solomon Islands, Wallis Islands, Irian Jaya, China.


Author(s):  

Abstract A new distribution map is provided for Maruca testulalis[Maruca vitrata] (Geyer) (including M. t. amboinalis Felder) (Lep., Pyralidae) (Bean Pod Borer, Mung Moth). Host Plants: Cajanus, Canavalia, Dolichos, Phaseolus, Vigna and other legumes. Information is given on the geographical distribution in ASIA, Andaman Islands, Bangladesh, Burma, Cambodia, China, Hongkong, India, Indonesia, Japan, Korea, Laos, Malaysia, Maldive Islands, Nepal, Nicobar Islands, Philippines, Ryukyu Islands, Sikkim, Singapore, Sri Lanka, Taiwan, Thailand, Vietnam, North AFRICA, Angola, Burundi, Dahomey, Fernando Po, Gabon, Ghana, Ivory Coast, Kenya, Madagascar, Malawi, Mali, Mauritius, Mozambique, Niger, Nigeria, Réunion, Rhodesia, Rwanda, Senegal, Sierra Leone, Somalia, South Africa, Sudan, Tanzania, Togo, Uganda, Zaire, AUSTRALASIA and PACIFIC ISLANDS, Australia, Cook Islands, Fiji, Hawaii, Marianas Islands, Marquesas Islands, New Caledonia, New Hebrides, Papua New Guinea, Samoa, American, & Western Society Islands, Solomon Islands, Tubuai, Tonga, Irian Jaya, NORTH AMERICA, Mexico, CENTRAL AMERICA and WEST INDIES, SOUTH AMERICA, Argentina, Brazil, Colombia, Ecuador, French Guiana, Guyana, Paraguay, Peru, Surinam, Uruguay, Venezuela.


Author(s):  

Abstract A new distribution map is provided for Hemiberlesia lataniae (Sign.) (Aspidtotux lataniae Sign.) (Hem., Coccoidea) (Latania Scale). Host Plants: Acacia, almond, avocado, banana, coconut, guava, indigo, mango, rose, tung. Information is given on the geographical distribution in EUROPE, Crete, Greece, Italy, Malta, Portugal, Sicily, Spain, Yugoslavia, ASIA, China, Cyprus, Hong Kong, India, Indonesia, Iraq, Israel, Japan, Jordan, Lebanon, Pakistan, Philippines, Sinai, Singapore, Sri Lanka, Syria, Taiwan, Thailand, Turkey, AFRICA, Algeria, Angola, Cameroun, Canary islands, Cape Verde Islands, Dahomey, Egypt, Ethiopia, Ghana, Guinea, Ivory Coast, Kenya, Libya, Madagascar, Madeira, Malawi, Mali, Mauritius, Morocco, Mozambique, Nigeria, Principe, Réunion, Rhodesia, Rodriguez Is, St. Helena, São Tomé, Seychelles, Sierra Leone, Somalia, South Africa, Sudan, Tanzania, Togo, Tunisia, Uganda, Zaire, AUSTRALASIA and PACIFIC ISLANDS, Australia, Caroline Islands, Fiji, Hawaii, Johnston Island, New Caledonia, Western Samoa Solomon Islands, Tonga, Irian Jaya, NORTH AMERICA, Mexico, U.S.A, CENTRAL AMERICA and WEST INDIES, Guatemala, Panama, West Indies, SOUTH AMERICA, Argentina, Brazil, Chile, Galapagos Islands, Guyana, Peru, Venezuela.


Itinerario ◽  
2000 ◽  
Vol 24 (3-4) ◽  
pp. 173-191 ◽  
Author(s):  
Robert Aldrich

At the end of the Second World War, the islands of Polynesia, Melanesia and Micronesia were all under foreign control. The Netherlands retained West New Guinea even while control of the rest of the Dutch East Indies slipped away, while on the other side of the South Pacific, Chile held Easter Island. Pitcairn, the Gilbert and Ellice Islands, Fiji and the Solomon Islands comprised Britain's Oceanic empire, in addition to informal overlordship of Tonga. France claimed New Caledonia, the French Establishments in Oceania (soon renamed French Polynesia) and Wallis and Futuna. The New Hebrides remained an Anglo-French condominium; Britain, Australia and New Zealand jointly administered Nauru. The United States' territories included older possessions – the Hawaiian islands, American Samoa and Guam – and the former Japanese colonies of the Northern Marianas, Mar-shall Islands and Caroline Islands administered as a United Nations trust territory. Australia controlled Papua and New Guinea (PNG), as well as islands in the Torres Strait and Norfolk Island; New Zealand had Western Samoa, the Cook Islands, Niue and Tokelau. No island group in Oceania, other than New Zealand, was independent.


1968 ◽  
Vol 57 (4) ◽  
pp. 567-604 ◽  
Author(s):  
R. W. Paine

The stick-insect Graeffea crouanii (Le Guillou) is a pest of coconuts of local and sporadic importance in the south Pacific and there have been recent outbreaks on Taveuni Island, in the Fiji group. As there appear to be virtually no parasites of the nymphal stages, a preliminary search was made in 1960 for parasites of other palm-feeding Phasmatids in Melanesia. This revealed the presence of Tachinidae parasitising species of the genera Ophicrania and Megacrania, and in 1963–64 these were studied in the Solomon Islands. The Tachinidae comprise at least two species of Mycteromyiella: M. laetifica (Mesnil) attacking both O. leveri Günth. and a species of Megacrania in the western Solomons, and M. phasmatophaga Crosskey attacking 0. leveri and some other Phasmatid hosts on Guadalcanal. The early stages of both species of Mycteromyiella are briefly described and compared, with notes on their bionomics. There was no evidence of any egg parasite attacking Ophicrania in the Solomons.O. leveri, which is very closely related to G. crouanii, has never caused significant damage to coconuts in the Solomon Islands, except on the small island of Savo, from which its Tachinid parasites appear to be absent. It is concluded that Mycteromyiella, especially M. laetifica, which appears to be fairly specific, may be an important factor in the control of O. leveri in the Solomons.The principal hosts of O. leveri are the sago palm (Metroxylon salomonense) and species of arecoid palms in the forest, on all of which the insect has better scope for concealment than on coconuts. Collections of nearly 6,000 examples of O. leveri from sago palm on Kolombangara island, in the western Solomons, in August 1963-February 1964 showed an average parasitism by Mycteromyiella laetifica of 28 per cent. Eggs of the Tachinid are laid on nymphs of all instars as well as on adults. The host-survival rate was about 30 per cent, for nymphs and 50 per cent, for adults.A small number of parasitised specimens of O. leveri from Kolombangara were released on Savo, but there was no evidence six months later that M. laetifica had become established there.Breeding trials at Honiara showed that O. leveri could be reared successfully in captivity but not M. laetifica, which shows reluctance to mate in cages and has a narrow range of environmental tolerance in the pupal stage, in which a mortality of at least 70 per cent, seems unavoidable under the conditions practicable for transportation of this stage by air.Between October 1963 and March 1964 nearly 960 puparia of M. laetifica were sent to Fiji. About half of them were used for breeding trials, which showed that the Tachinid could be reared through G. crouanii in captivity but could not be maintained. The rest were released on Taveuni, but a further outbreak of G. crouanii during 1965 yielded no evidence that M. laetifica had become established.Material of M. phasmatophaga, which has a more restricted choice of environment than M. laetifica, but also a somewhat greater potentiality for killing its host, was obtained by exposing O. leveri on seedling coconut palms planted in the forest at Honiara. Quantities were insufficient for transmission to Fiji; 150 parasitised hosts were released on Savo but samples of O. leveri collected there six months later gave no indication of its establishment.Despite this initial failure, it is considered that Mycteromyiella could bring about the control of G. crouanii in Fiji and other affected Pacific islands, and the means by which this might be achieved are discussed.


2005 ◽  
Vol 86 (2) ◽  
pp. 491-499 ◽  
Author(s):  
Peter Revill ◽  
Xuan Trinh ◽  
James Dale ◽  
Rob Harding

Sequencing of the monopartite RNA genome of a Fijian isolate of Taro vein chlorosis virus (TaVCV) confirmed that it is a definitive rhabdovirus with most similarity to members of the genus Nucleorhabdovirus. The TaVCV 12 020 nt negative-sense RNA genome contained six ORFs in the antigenomic sequence, equivalent to the N, P, 3, M, G and L genes that have been identified in other rhabdoviruses. The putative gene products had highest similarity to those of the nucleorhabdovirus Maize mosaic virus. A characteristic 3′-AAUUCUUUUUGGGUUGU/A-5′ sequence was identified in each of the intergenic regions and the TaVCV leader and trailer sequences comprised 140 and 61 nt, respectively. Assignment of TaVCV to the genus Nucleorhabdovirus was supported by thin-section electron microscopy of TaVCV-infected taro leaves, which identified virions budding from nuclear membranes into the perinuclear space. Variability studies identified high levels of TaVCV sequence diversity. Within the L gene of 20 TaVCV isolates from Fiji, the Federated States of Micronesia, New Caledonia, Papua New Guinea, Solomon Islands and Vanuatu, maximum variability at the nucleotide level was 27·4 %. Within the N gene, maximum variability among 15 isolates at the nucleotide level was 19·3 %. The high level of TaVCV variability observed suggested that the introduction of TaVCV to the Pacific Islands was not a recent occurrence.


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