Observations of the 'Critically Endangered' bare-rumped sheathtail bat Saccolaimus saccolaimus Temminck (Chiroptera: Emballonuridae) on Cape York Peninsula, Queensland.

2001 ◽  
Vol 23 (2) ◽  
pp. 185 ◽  
Author(s):  
S Murphy

THE bare-rumped sheathtailed bat Saccolaimus saccolaimus is a poorly understood species that has a wide distribution covering parts of India, Sri Lanka, Thailand, Myanmar, Malaya, Indonesia, New Guinea, the Solomon Islands and Northern Australia (Bonaccorso 1998). First collected in Australia by De Vis near Cardwell, the current known distribution in Queensland (Qld) extends from Bowen to Cooktown with one isolated specimen collected near Coen on Cape York Peninsula (Hall 1995; Duncan et al. 1999). It has also been recorded in the Alligator River area in the Northern Territory (McKean et al. 1981). The conservation status of S. saccolaimus in Qld has recently been defined as ?Critically Endangered?, and the species has not been recorded anywhere in Australia for at least 18 years (Duncan et al. 1999; Menkhorst and Knight 2001). The likely reasons for the apparent decline are unclear, but may involve land-clearing and changed fire regimes in the coastal zone where it is thought to occur (Duncan et al. 1999). In contrast, Bonaccorso (1998) considers S. saccolaimus to be secure, albeit also poorly known in Papua New Guinea.


Author(s):  
D. W. Minter

Abstract C. brasiliense is described and illustrated. Information on symptoms of the disease caused by C. brasiliense, host range (mainly horticultural and field crops, trees, wood, man, dung and artefacts), geographical distribution (Democratic Republic of Congo; Ghana; Namibia; Nigeria; Tanzania; Swaziland; Ontario, Canada; California, Kansas, New Mexico and Texas, USA; Pernambuco, Brazil; Ecuador; Bangladesh; India; Japan; Malaysia; Pakistan; Papua New Guinea; Philippines; Russia; Sri Lanka; Thailand; Northern Territory, Australia; Great Britain; Kuwait; Spain; Saudi Arabia; and Solomon Islands), transmission, biology and conservation status is presented.



Author(s):  

Abstract A new distribution map is provided for Phyllosticta maculata Wong & Crous. Dothideomycetes: Phyllostictaceae. Hosts: banana (Musa spp.). Information is given on the geographical distribution in Asia (Indonesia, Java, Sulawesi, Malaysia, Sarawak, Philippines), Oceania (American Samoa, Australia, Northern Territory, Queensland, Fiji, Palau, Papua New Guinea, Samoa, Solomon Islands).



2020 ◽  
Vol 8 (1) ◽  
pp. 37-45
Author(s):  
KONSTANTINA M. B KAMEUBUN ◽  
ROSANIA REHIARA ◽  
FRANS DEMINGGUS

Ethnobotanical and taxonomical studies are conducted to uncover the scientific name, uses as well as utilization of Diwoka (local name) popular to the Dani people in Wamena. The local name, Diwoka, is determined by its scientific name Piper macropiper Pennant. Piper macropiper has been used by the Dani people to serve as spices when foods are cooked traditionally by stone-fired earth oven (bakarbatu) or prepared in other ways such as stir-frying vegetables, fish, and meat. The leaves can be consumed uncooked the way salad is consumed beside it is functioned as medicine as well. The distribution of this type of plant is found in Indonesia, Papua New Guinea, Solomon Islands, Australia (Northern territory), Brunei, and Sri Lanka



1989 ◽  
Vol 20 (1) ◽  
pp. 75-120 ◽  
Author(s):  
N. Møller Andersen

AbstractMarine bugs of the genus Halovelia Bergroth inhabit intertidal coral reefs and rocky coasts along the continents and larger islands bordering the Red Sea, Indian Ocean, and western Pacific Ocean as well as on island groups and atolls in these areas. A historical review of the study of the genus is presented and different views upon its classification discussed. The genus Halovelia is redescribed together with its type species, H. maritima Bergroth, and four other previously known species. Fifteen new species are described: H. carolinensis sp.n. (Caroline Islands), H. halophila sp.n. (Sumbawa, Sabah), H. corallia sp.n. (Papua New Guinea, Australia: Queensland), H. esakii sp.n. (Solomon Islands, Irian New Guinea, Moluccas, Sulawesi, Sumbawa, Palau Islands, Philippines), H. polhemi sp.n. (Australia: Northern Territory), H. solomon sp.n. (Solomon Islands), H. novoguinensis sp.n. (Papua New Guinea), H. fosteri sp.n. (Fiji Islands), H. tongaensis sp.n. (Tonga Islands), H. heron sp.n. (Australia: S. Queensland), H. fijiensis sp.n. (Fiji Islands), H. inflexa sp.n. (Sudan, Red Sea), H. annemariae sp.n. (Solomon Islands, Papua New Guinea), H. lannae sp.n. (Java, Singapore, West Malaysia, Sabah, Philippines), and H. wallacei sp.n. (Sulawesi, Sumbawa). Two names are synonymized: H. marianarum Usinger syn.n. (= H. bergrothi Esaki) and H. danae Herring syn.n. (= H. bergrothi Esaki). The following species are removed from the genus Halovelia: H. papuensis Esaki, H. loyaltiensis China, and H. (Colpovelia) angulana Polhemus. A key to the species is included. The taxonomy of the H. malaya-group will be presented in Part II of this work together with the cladistics, ecology, biology, and biogeography of the genus.



1992 ◽  
Vol 5 (5) ◽  
pp. 533 ◽  
Author(s):  
PI Forster

Circumscription of the genus Ichnocarpus R. Br. is discussed and Micrechites Miq. and Lamechites Markgraf are placed in synonymy. Ichnocarpus R. Br. is revised for Australia and Papuasia (Irian Jaya, Papua New Guinea and the Solomon Islands). Three species are recognised in this region, namely I. archboldianus comb. nov. (Micrechites archboldiana Merr. & Perr.), I. frutescens (L.) W. T. Aiton and I. serpyllifolius comb. nov. (Ficus serpyllifolia Blume). Lumechites schlechteri Markgraf, Micrechites rhombifolia Markgraf, M. rhombifolia var. lanceolata Markgraf and Ichnocarpus salornonensis C. T. White are newly placed in the synonymy of Ichnocarpus serpyllifolius. The new combination I. polyanthus (Micrechites polyantha Miq.) is made for a Malesian species west of Papuasia. The names Ichnocarpus leptodictyus F. Muell. and Micrechites rhombifolia Markgraf are lectotypified. Generic and specific descriptions, a species key, notes on variation, distribution, habitat and conservation status are provided.



Author(s):  

Abstract A new distribution map is provided for Sweet potato little leaf phytoplasma Bacteria: Phytoplasmas Hosts: Sweet potato (lpomoea batatas). Information is given on the geographical distribution in ASIA, Bangladesh, China, Fujian, India, Indonesia, Nusa Tenggara, Japan, Ryukyu Archipelago, North Korea, Korea Republic, Malaysia, Sarawak, Philippines, Taiwan, OCEANIA, Australia, Northern Territory Queensland, Fed. States of Micronesia, New Caledonia, Niue, Palau, Papua New Guinea, Solomon islands, Tonga, Vanuatu.



1986 ◽  
Vol 76 (4) ◽  
pp. 701-717 ◽  
Author(s):  
R. G. Booth ◽  
R. D. Pope

AbstractCryptolaemus montrouzieri Mulsant is a well-known and historically important predator of mealybugs. It is indigenous to eastern Australia, and has been introduced throughout the world for biological control. In contrast, the other members of the genus, including those which resemble C. montrouzieri, remain poorly known. The genus Cryptolaemus, with seven previously described species, is redefined and two species-groups are recognized. The first, the montrouzieri group, comprising C. montrouzieri, C. affinis Crotch (Indonesia and Papua New Guinea and northern Queensland, Australia). C. wallacei Crotch (Indonesia) and C. simplex Blackburn (northern Australia), is revised; C. crotchi sp. n. (Indonesia) and C. sinestria sp. n. (Indonesia, Papua New Guinea and Solomon Islands) are described as new, and C. simplex is reduced to a subspecies of C. montrouzieri. A key to these species is provided. The second group comprises two of the remaining species. C. subviolaceus Crotch and C. concinnus Weise, but lack of sufficient material precludes a revision of this group at present. The final species, C. engelhardi Gorham. is transferred to the chilocorine genus Brumoides Chapin. Lectotypes are selected where appropriate.



Viruses ◽  
2021 ◽  
Vol 13 (3) ◽  
pp. 482
Author(s):  
Alice Michie ◽  
John S. Mackenzie ◽  
David W. Smith ◽  
Allison Imrie

Ross River virus (RRV) is the most medically significant mosquito-borne virus of Australia, in terms of human morbidity. RRV cases, characterised by febrile illness and potentially persistent arthralgia, have been reported from all Australian states and territories. RRV was the cause of a large-scale epidemic of multiple Pacific Island countries and territories (PICTs) from 1979 to 1980, involving at least 50,000 cases. Historical evidence of RRV seropositivity beyond Australia, in populations of Papua New Guinea (PNG), Indonesia and the Solomon Islands, has been documented. We describe the genomic characterisation and timescale analysis of the first isolate of RRV to be sampled from PNG to date. Our analysis indicates that RRV has evolved locally within PNG, independent of Australian lineages, over an approximate 40 year period. The mean time to most recent common ancestor (tMRCA) of the unique PNG clade coincides with the initiation of the PICTs epidemic in mid-1979. This may indicate that an ancestral variant of the PNG clade was seeded into the region during the epidemic, a period of high RRV transmission. Further epidemiological and molecular-based surveillance is required in PNG to better understand the molecular epidemiology of RRV in the general Australasian region.



1994 ◽  
Vol 11 (1) ◽  
pp. 179-192
Author(s):  
Victor Prescott


Author(s):  

Abstract A new distribution map is provided for Rice grassy stunt tenuivirus Viruses: Tenuivirus. Hosts: Rice (Oryza sativa). Information is given on the geographical distribution in ASIA, Bangladesh, Brunei, Darussalam, China, India, Kerala, Tamil Nadu, Indonesia, Java, Nusa, Tenggara, Sulawesi, Sumatra, Japan, Kyushu, Korea Republic, Malaysia, Philippines, Sri Lanka, Taiwan, Thailand, Vietnam, OCEANIA, Fiji, Papua New Guinea, Solomon Islands.



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