A brief historical account of an endemic swallowtail butterfly first collected a century ago on Goodenough Island (D'Entrecasteaux group) in Papua New Guinea

2017 ◽  
Vol 44 (1) ◽  
pp. 159-169
Author(s):  
W. J. Tennent ◽  
D. K. Mitchell

Graphium weiskei goodenovii Rothschild, 1915 (Lepidoptera: Papilionidae) has been known for over a century only from two male specimens: one in the Natural History Museum, London; the other in the Oxford University Museum of Natural History (OUMNH). Endemic to Goodenough Island, in the D'Entrecasteaux group, Papua New Guinea, it was first collected on the summit of ‘Oiamadawa'a (Mount Madawaa, Mount Madara'a) in 1912 by New Zealand anthropologist Diamond Jenness. The second specimen, which became the holotype, was collected in mountains in the south of the island by Albert Stewart Meek, one of Walter, Lord Rothschild's most prolific collector/explorers for his museum at Tring in Hertfordshire. In each case, capture of specimens was sufficiently notable to be recorded contemporaneously by the captors. These data, and maps and photographs made by the collectors suggest that the butterfly was widespread at moderate to high elevations on Goodenough Island. The authors climbed ‘Oiamadawa'a in 2015 and collected further specimens, now deposited in OUMNH.

Zootaxa ◽  
2020 ◽  
Vol 4729 (2) ◽  
pp. 151-176
Author(s):  
FELIPE VIVALLO

In this paper the primary types of Centris bees described by the British entomologist Frederick Smith deposited in the Natural History Museum, London and in the Oxford University Museum of Natural History, Oxford, United Kingdom were studied. To stabilize the application of some names, lectotypes were designated for C. agilis, C. apiformis (= C. aenea Lepeletier), C. ardens (= C. varia (Erichson)), C. aterrima, C. cineraria, C. concinna (= C. dentata), C. crassipes, C. dentata, C. difformis, C. discolor, C. elegans, C. ephippium, C. festiva, C. ignita (= C. agilis), C. insignis, C. insularis, C. maculifrons, C. melanochlaena, C. mexicana, C. modesta, C. nitida, C. perforator, C. personata (= C. longimana Fabricius), C. plumipes, C. rubella (= C. ferruginea Lepeletier), C. semicaerulea, C. simillima, C. tarsata, C. thoracica (= C. domingensis Dalla Torre) and Anthophora dimidiata (= C. nigerrima (Spinola)). Centris perforator nom. rev. and C. modesta nom. rev. are withdrawn from the synonymy of C. fuscata Lepeletier and C. obsoleta Lepeletier respectively, and consequently revalidated. Centris fulviventris Cresson and C. simillima are removed from the synonymy of C. lanipes (Fabricius), proposing the revalidation of the first species and the second one as its new junior synonym. Centris insignis and C. insignis scutellaris Friese are proposed as new junior synonyms of C. laticincta (Spinola). The critical study of the primary type of C. aterrima, for a long time a misidentified species, allowed for proposing C. anomala Snelling as its new junior synonym. As result of this synonymy, C. apache new species is here described based on specimens incorrectly considered as belonging to C. aterrima. In addition, a lectotype for Centris clypeata Friese (= C. nigrocaerulea Smith) is also designated. 


Zootaxa ◽  
2007 ◽  
Vol 1502 (1) ◽  
pp. 1-44 ◽  
Author(s):  
HEIKKI HIPPA

The following new species of Manota are described: M. biunculata (Papua New Guinea), M. evexa (Papua New Guinea), M. explicans (Papua New Guinea), M. gemella (Ambon, Maluku Utara, Indonesia), M. hirsuta (Papua New Guinea), M. orthacantha (Papua New Guinea), M. parilis (Papua New Guinea), M. pentacantha (Solomon Islands), M. perissochaeta (Papua New Guinea and Solomon Islands), M. serawei (Papua New Guinea), M. sicula (Papua New Guinea), M. spathula (Papua New Guinea), M. subspathula (Papua New Guinea) and M. tricuspis (Fiji). Manota ctenophora Matile (New Caledonia), M. maorica Edwards (New Zealand) and M. taedia Matile (New Caledonia) are redescribed. Manota hamulata Colless, previously known from Palau, is redescribed and recorded from Papua New Guinea. Manota pacifica Edwards from Samoa is discussed and compared with the other species of the region. A key to the Melanesian and Oceanian species of Manota is given.


ZooKeys ◽  
2019 ◽  
Vol 823 ◽  
pp. 1-126
Author(s):  
Catherine A. Tauber ◽  
Zoë Simmons ◽  
Agatha J. Tauber

The Hope Entomological Collection in the Oxford University Museum of Natural History holds a large and diverse array of historically valuable type specimens for species in the superorder Neuropterida (Megaloptera, Neuroptera, and Raphidioptera). Most are from the mid-1800s (1823–1874). Here, we report each type found during a rigorous search of the collection, and we confirm the identity and status of each type with bibliographic, specimen, and label data. Images, current nomenclatural information, and references for name changes are provided for each species.We identified primary or secondary types for 76 species in seven families of Neuroptera, primary and secondary types for one species of Raphidoptera (Raphidiidae), and secondary types for three species of Megaloptera (Corydalidae). Among the Neuroptera, we found primary types for 26 species of Mantispidae, 16 species of Myrmeleontidae, 11 species of Ascalaphidae, seven species of Nemopteridae, five species of Chrysopidae, and one species each of Coniopterygidae and Hemerobiidae. Types for only two species that were reported to be in the collection were not found.To help stabilize the nomenclature, we made new lectotype designations for the following six species in the Hope Collection:ColobopterusdissimilisMcLachlan, 1871;MantispabatesellaWestwood, 1867;MantispamyrapetrellaWestwood, 1867;MantispatropicaWestwood, 1852;MyrmeleonanomalusRambur, 1842; andMyrmeleonsingulareWestwood, 1847. We also made new lectotype designations for two species in the Natural History Museum in London:MantispaindicaWestwood, 1852, andMantispaquadrituberculataWestwood, 1852. In several other cases, holotype determinations in the literature were recognized as lectotype designations. Finally, to correct an important error in the literature, we reinstated the synonymization ofAscalaphusanticusWalker, 1853,A.loquaxWalker, 1853, andA.truxWalker, 1853 underA.longusWalker, 1853.


Zootaxa ◽  
2017 ◽  
Vol 4277 (2) ◽  
pp. 295
Author(s):  
MÁRCIA S. COURI ◽  
ADRIAN C. PONT

Spilogona breviaristata sp. nov. from South Africa is described and the morphology of the male terminalia of seven African Spilogona Schnabl (Diptera, Muscidae) species are described and illustrated: Spilogona biguttata Emden, Spilogona fuscotriangulata Emden, Spilogona natalensis Zielke, Spilogona pertinisetodes Emden, Spilogona quasifasciata Emden, Spilogona semifasciata Emden and Spilogona spinipes (Bigot). The material studied is deposited in the Natural History Museum (BMNH), London, United Kingdom, and paratypes of the new species are also in the Museu Nacional, Universidade Federal do Rio de Janeiro (MNRJ), Rio de Janeiro, Brazil, and the Oxford University Museum of Natural History (OUMNH), Oxford, United Kingdom. 


2018 ◽  
Vol 154 (3) ◽  
pp. 179-196
Author(s):  
Michael Darby

Some 2,000 Ptiliidae collected in the North and South Islands of New Zealand in 1983/1984 by Peter Hammond of the Natural History Museum, London, are determined to 34 species, four of which are new to the country. As there are very few previous records, most from the Auckland district of North Island, the Hammond collection provides much new distributional data. The three new species: Nellosana insperatus sp. n., Notoptenidium flavum sp. n., and Notoptenidium johnsoni sp. n., are described and figured; the genus Ptiliodes is moved from Acrotrichinae to Ptiliinae, and Ptenidium formicetorum Kraatz recorded as a new introduction. Information is provided to aid separation of the new species from those previously recorded.


1866 ◽  
Vol 5 ◽  
pp. 444-449
Author(s):  
Wm. Turner

1st, Scaphocephalus.—After making reference to his previous papers, more especially to that in which he had described several specimens of the scaphocephalic skull, in which he had discussed the influence exercised on the production of deformities of the cranium, by a premature closure or obliteration of the sutures, and to the recent memoirs of Professor von Düben of Stockholm,† and Dr John Thurnam, the author proceeded to relate two additional cases of scaphocephalus to those he had already recorded. He had met with one of these in the head of a living person, the other in a skull in the Natural History Museum of the University of Edinburgh.


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.


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.


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