History of Tuberculosis in Australia, New Zealand and Papua New Guinea

1992 ◽  
Vol 116 (2) ◽  
pp. 175
2021 ◽  
pp. 0310057X2110278
Author(s):  
Terence E Loughnan ◽  
Michael G Cooper ◽  
Pauline B Wake ◽  
Harry Aigeeleng

The most recent estimates, published in 2016, have indicated that around 70% of anaesthesia providers in Papua New Guinea are non-physician anaesthetic providers and that they administer over 90% of anaesthetics, with a significant number unsupervised by a physician anaesthetist. Papua New Guinea has a physician anaesthetist ratio estimated to be 0.25 per 100,000 population, while Australia and New Zealand have a ratio of 19 physician anaesthetists per 100,000, which is 75 times that of Papua New Guinea. To reach a ratio of seven per 100,000, recommended as the minimum acceptable by the Lancet Commission in 2016, there will need to be over 35 practitioners trained per annum until 2030, at a time when the average annual numbers of recent years are less than three physicians and less than five non-physician anaesthetic providers. We review the development of anaesthesia administered by non-physician indigenous staff and the stages of development from heil tultuls, dokta bois, liklik doktas, native medical assistants, aid post orderlies, and Anaesthetic Technical Officers up to the current Anaesthetic Scientific Officers having attained the Diploma in Anaesthetic Science from the University of Papua New Guinea.


CHEST Journal ◽  
1992 ◽  
Vol 102 (4) ◽  
pp. 22 ◽  
Author(s):  
A.J. PROUST ◽  
Carlton R. Souders

Radiocarbon ◽  
2021 ◽  
pp. 1-21
Author(s):  
Chris Urwin ◽  
Quan Hua ◽  
Henry Arifeae

ABSTRACT When European colonists arrived in the late 19th century, large villages dotted the coastline of the Gulf of Papua (southern Papua New Guinea). These central places sustained long-distance exchange and decade-spanning ceremonial cycles. Besides ethnohistoric records, little is known of the villages’ antiquity, spatiality, or development. Here we combine oral traditional and 14C chronological evidence to investigate the spatial history of two ancestral village sites in Orokolo Bay: Popo and Mirimua Mapoe. A Bayesian model composed of 35 14C assays from seven excavations, alongside the oral traditional accounts, demonstrates that people lived at Popo from 765–575 cal BP until 220–40 cal BP, at which time they moved southwards to Mirimua Mapoe. The village of Popo spanned ca. 34 ha and was composed of various estates, each occupied by a different tribe. Through time, the inhabitants of Popo transformed (e.g., expanded, contracted, and shifted) the village to manage social and ceremonial priorities, long-distance exchange opportunities and changing marine environments. Ours is a crucial case study of how oral traditional ways of understanding the past interrelate with the information generated by Bayesian 14C analyses. We conclude by reflecting on the limitations, strengths, and uncertainties inherent to these forms of chronological knowledge.


Author(s):  
A. Sivanesan

Abstract A description is provided for Cochliobolus cynodontis. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: Cynodon dactylon (very common on this host), other Cynodon spp., Agropyron, Ammi, Arecastrum, Axonopus, Calathea, Chamaedorea, Chrysalidocarpus, Dactyloctenium, Eleusine, Hordeum, Ipomoea, Lycopersicon, Muhlenbergia, Oryza, Panicum, Pennisetum, Poa, Rhapis, Secale and Zea. DISEASE: Leafspot of Bermuda grass end other crops, leaf blight end brown patches of turf, lawns end golflinks. GEOGRAPHICAL DISTRIBUTION: Argentina, Australia, Bangladesh, Brazil, Brunei, Egypt, Ghana, Guinea, India, Israel, Iraq, Italy, Japan, Kenya, Malaysia, New Zealand, Pakistan, Papua New Guinea, Puerto Rico, Spain, South Africa, Sudan, Tanzania, Trinidad, Turkey, USA, USSR, Venezuela, Yugoslavia and Zambia. TRANSMISSION: By wind-borne conidia and seed-borne.


Author(s):  
A. Sivanesan

Abstract A description is provided for Cochliobolus eragrostidis. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: Acacia, Agave, Allium, Alysicarpus, Amorphophallus, Anacardium, Arachis, Areca, Billbergia, Calamus, Callitris, Calotropis, Camellia, Cananga, Capsicum, Citrullus, Citrus, Clerodendron, Cocos, Coffea, Colocasia, Cymbopogon, Dendrobium, Digitaria, Dioscorea, Dracaena, Durio, Elaeis, Eragrostis, Eucalyptus, Euphorbia, Furcraea, Gladiolus, Glycine, Gossypium, Heliconia, Hevea, Hystrix, Ipomoea, Kaempferia, Lycopersicon, Mangifera, Manihot, Mystroxylon, Musa, Neyraudia, Oldenlandia, Opuntia, Oryza, Panicum, Pennisetum, Pentas, Phalaenopsis, Phaseolus, Pinus, Polygala, Pueraria, Raphia, Raphanus, Rhodomyrtus, Rhoeo, Rottboellia, Saccharum, Sesamum, Sorghum, Spinacia, Sporobolus, Stylosanthes, Theobroma, Thrasya, Tradescantia, Trichosanthes, Triplochiton, Triticum, Vanda, Vigna, Zea, Zingiber and soil. DISEASE: Leaf spots. GEOGRAPHICAL DISTRIBUTION: Australia, Bangladesh, Belize, Brazil, Brunei, Burma, Colombia, Cuba, Fiji, Ghana, Guinea, Honduras, Hong Kong, India, Indonesia, Japan, Kenya, Kuwait, Malaysia, New Zealand, Nigeria, Papua New Guinea, Puerto Rico, Sierra Leone, Singapore, Solomon Islands, Sri Lanka, Trinidad, USA, Zambia, Zaire. TRANSMISSION: By wind-borne conidia.


2001 ◽  
Vol 36 (4) ◽  
pp. 321-340 ◽  
Author(s):  
Koen Sabbe ◽  
Koenraad Vanhoutte ◽  
Rex L. Lowe ◽  
Elizabeth A. Bergey ◽  
Barry J.F. Biggs ◽  
...  

2010 ◽  
Vol 40 (6) ◽  
pp. 1271-1279 ◽  
Author(s):  
Barnaby J. Dixson ◽  
Paul L. Vasey ◽  
Katayo Sagata ◽  
Nokuthaba Sibanda ◽  
Wayne L. Linklater ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document