Appendices Image on Reverse: Australian Old Endemic Rodent, Leggadina Lakedownensis

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Appendices Image on reverse: Australian Old Endemic rodent, Leggadina lakedownensis. Modified image from Strahan, 2002 Appendix 1: Nucleotide sequence of exon 6, intron 6 and exon 7 of Zp3 from New Guinean and Australasian murine rodents. Exons are indicated in bold. Polymorphic sites are highlighted in grey.

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NHBSS 054 2G Wattanaratcha
NAT. NAT. HIST. BUL L. SIAM Soc. 54(2): 195-207 ，2006 SMALL MAMMALS AROUND A KAREN VILLAGE IN NORTHERN MAE HONG SON PROVINCE ，THAILAND: ABUNDANCE ，DISTRIBUTION AND HUMAN CONSUMPTION Nattha Nattha Wattanaratchaki t' and Sompoad Srikosamatarcl ABSTRACT The aim of 出is study was to understand the ecology of small mammals around a Karen village village and the relationships between small mammals and the lifestyle of the Karen people. Th e abundance ，distribution and species diversity of small mammals were studied around a Ka 民 n village ，Muang Pham ， Pang Ma Pa District ， in Mae Hong Son Province. Ten species were captured. captured. Menetes berdmorei ， Rattus rattus ，如 d Niviventer bukit were the most common species around around the village. R. rattus w ぉ abundant in paddy fields ， whereas M. berdmorei was captu 問 d more often in com fields. N. bukit was most common in multiple-use forest area. 明le highest abundance abundance of small mammals was found in 恥 agricultural area ，whereas 曲eir gl 四回 tspecies diversity diversity was in the community fores t. Most species that occur 四 d in the agricultural 蹴 a were pest pest species. Maxomys su ゆ r had low density around the village but was a valuable source of of protein for Karen villagers. About 3，000 raωweighing a to 飽1 of more 血an 300 kg we 問 ∞nsumed in Muang Pham village during November 20 04- January 2005. Disturbance from agriculture ， and harvest of timber and non-timber forest products around the village have caused caused a high abundance of pest species around 白is Karen village.
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BANDICOTA INDICA, the BANDICOOT RAT 3.1 The
CHAPTER THREE BANDICOTA INDICA, THE BANDICOOT RAT 3.1 The Living Animal 3.1.1 Zoology Rats and mice (family Muridae) are the most common and well-known rodents, not only of the ﬁ elds, cultivated areas, gardens, and storage places but especially so of the houses. Though there are many genera and species, their general appearance is pretty the same. Rats are on average twice as large as mice (see Chapter 31). The bandicoot is the largest rat on the Indian subcontinent, with a body and head length of 30–40 cm and an equally long tail; this is twice as large as the black rat or common house rat (see section 3.1.2 below). This large size immediately distinguishes the bandicoot from other rats. Bandicoots have a robust form, a rounded head, large rounded or oval ears, and a short, broad muzzle. Their long and naked scaly tail is typical of practically all rats and mice. Bandicoots erect their piles of long hairs and grunt when excited. Bandicoots are found practically on the whole of the subcontinent from the Himalayas to Cape Comorin, including Sri Lanka, but they are not found in the deserts and the semi-arid zones of north-west India. Here, they are replaced by a related species, the short-tailed bandicoot (see section 3.1.2 below). The bandicoot is essentially parasitic on man, living in or about human dwellings. They cause a lot of damage to grounds and ﬂ oorings because of their burrowing habits; they also dig tunnels through bricks and masonry.
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Biogeography of Mammals in SE Asia: Estimates of Rates of Colonization, Extinction and Speciation
Biological Journal oflhe Linnean Sociely (1986), 28, 127-165. With 8 figures Biogeography of mammals in SE Asia: estimates of rates of colonization, extinction and speciation LAWRENCE R. HEANEY Museum of <oology and Division of Biological Sciences, University of Michigan, Ann Arbor, Michigan 48109, U.S.A. Accepted for publication I4 February 1986 Four categories of islands in SE Asia may be identified on the basis of their histories of landbridge connections. Those islands on the shallow, continental Sunda Shelf were joined to the Asian mainland by a broad landbridge during the late Pleistocene; other islands were connected to the Sunda Shelf by a middle Pleistocene landbridge; some were parts of larger oceanic islands; and others remained as isolated oceanic islands. The limits of late Pleistocene islands, defined by the 120 ni bathymetric line, are highly concordant with the limits of faunal regions. Faunal variation among non-volant mammals is high between faunal regions and low within the faunal regions; endcmism of faunal regions characteristically exceeds 70%. Small and geologically young oceanic islands are depauperate; larger and older islands are more species-rich. The number of endemic species is correlated with island area; however, continental shelf islands less than 125000 km2 do not have endemic species, whereas isolated oceanic islands as small as 47 km2 often have endemic species. Geologirally old oceanic islands have many endemic species, whereas young oceanic islands have few endemic species. Colonization across sea channels that were 5-25 km wide during the Pleistocene has been low, with a rate of about 1-2/500000 years.
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Calaby References
Abbott, I.J. (1974). Natural history of Curtis Island, Bass Strait. 5. Birds, with some notes on mammal trapping. Papers and Proceedings of the Royal Society of Tasmania 107: 171–74. General; Rodents; Abbott, I. (1978). Seabird islands No. 56 Michaelmas Island, King George Sound, Western Australia. Corella 2: 26–27. (Records rabbit and Rattus fuscipes). General; Rodents; Lagomorphs; Abbott, I. (1981). Seabird Islands No. 106 Mondrain Island, Archipelago of the Recherche, Western Australia. Corella 5: 60–61. (Records bush-rat and rock-wallaby). General; Rodents; Abbott, I. and Watson, J.R. (1978). The soils, flora, vegetation and vertebrate fauna of Chatham Island, Western Australia. Journal of the Royal Society of Western Australia 60: 65–70. (Only mammal is Rattus fuscipes). General; Rodents; Adams, D.B. (1980). Motivational systems of agonistic behaviour in muroid rodents: a comparative review and neural model. Aggressive Behavior 6: 295–346. Rodents; Ahern, L.D., Brown, P.R., Robertson, P. and Seebeck, J.H. (1985). Application of a taxon priority system to some Victorian vertebrate fauna. Fisheries and Wildlife Service, Victoria, Arthur Rylah Institute of Environmental Research Technical Report No. 32: 1–48. General; Marsupials; Bats; Rodents; Whales; Land Carnivores; Aitken, P. (1968). Observations on Notomys fuscus (Wood Jones) (Muridae-Pseudomyinae) with notes on a new synonym. South Australian Naturalist 43: 37–45. Rodents; Aitken, P.F. (1969). The mammals of the Flinders Ranges. Pp. 255–356 in Corbett, D.W.P. (ed.) The natural history of the Flinders Ranges. Libraries Board of South Australia : Adelaide. (Gives descriptions and notes on the echidna, marsupials, murids, and bats recorded for the Flinders Ranges; also deals with the introduced mammals, including the dingo).
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Retrotransposons
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TAXONOMIC STUDIES from RODENT OUTBREAK AREAS in the CHITTAGONG HILL TRACTS Nikhil
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