Comparative Parasitology 67(1) 2000 - Peru State College

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58 COMPARATIVE PARASITOLOGY, <strong>67</strong>(1), JANUARY <strong>2000</strong> Figures 22—31. Popovastrongylus pluteus sp. n. from Macropus robustus. 22. Anterior end (lateral view). 23. Cephalic end, optical section (lateral view). 24. Mouth opening (en face view). 25. Cephalic end, optical section (ventral view). 26. Cephalic collar (lateral view). 27. Buccal capsule, transverse optical section at level of shelf. 28. Bursa (ventral view). 29. Bursa (lateral view). 30. Ovejector (lateral view). 31. Female posterior end (lateral view). Scale bars: Figures 22, 31 = 200 urn; Figures 23, 25, 26 = 25 |xm; Figures 24, 27 = 10 urn; Figures 28, 29 = 50 (mm; Figure 30 = 100 |xm. in red-necked wallabies from New South Wales, Victoria, or South Australia. This may be because of either a lack of sampling effort (the parasite being present but not detected) or a disjunct distribution of the parasite. Popovastrongylus pearsoni also occurs in red-necked wallabies from the same localities in Tasmania as P. wallabiae and has only been found on con- Copyright © 2011, The Helminthological Society of Washington tinental Australia in a common wallaroo in the Tidbinbilla Nature Reserve in the Australian Capital Territory. Since the macropod population on the reserve includes red-necked wallabies, tammars, and species of rock-wallaby, it is reasonable to suppose that this record was an accidental infection. It does, however, occur in 3 other hosts, the tammar and western grey kan-
garoo from Kangaroo Island (Smales and Mawson, 1978; Beveridge, 1986) and Petrogale lateralis Gould, 1842, the black-footed wallaby from Pearson Island (Johnston and Mawson, 1940; Mawson, 1971; Beveridge, 1986), both southern localities offshore from South Australia. Popovastrongylus irma is found only in the western brush wallaby in southwestern Australia (Mawson, 1977), but in contrast to P. pearsoni it has not been reported from sympatric hosts in the region. In general, species of Popovastrongylus infect mainly pademelons and the small wallabies, M. irma, M. eugenii, and M. rufogriseus. The genus is not common in the larger kangaroos from northern Queensland, with only 1 or 2 nematodes present in each individual host (Beveridge, 1986) and does not normally occur in kangaroos in the southern states (Beveridge and Arundel, 1979; Arundel et al., 1979, 1990). Neither is the genus found in Wallabia bicolor, the swamp wallaby (Beveridge et al., 1985), nor the macropodid genera Hypsiprymnodon, Aepyprymnus, Onychogalea, Lagorchestes, or Dendrolagus (Beveridge et al., 1992). Acknowledgments My thanks go to Ms. J. Forrest from the South Australian Museum for making material available and to Dr. I. Beveridge for his unfailing help and generosity. Literature Cited Arundel, J. H., I. Beveridge, and P. J. Presidente. 1979. Parasites and pathological findings in enclosed and free-ranging populations of Macropus rufiis (Desmarest) (Marsupialia) at Menindee, New South Wales. Australian Wildlife Research 6:361-379. , K. J. Dempster, K. E. Harrigan, and R. Black. 1990. Epidemiological observations on the helminth parasites of Macropus giganteus Shaw in Victoria. Australian Wildlife Research 17:39- 51. Begg, M., I. Beveridge, N. B. Chilton, P. M. Johnson, and M. G. O'Callaghan. 1995. Parasites of the Proserpine rock wallaby, Petrogale persepho- SMALES—POPOVASTRONGYLUS FROM MARSUPIALS 59 ne (Marsupialia: Macropodidae). Australian Mammalogy 18:45-53. Beveridge, I. 1986. New species and new records of Popovastrongylus Mawson, 1977 (Nematoda: Cloacininae) from Australian marsupials. Bulletin du Museum National d'Histoire Naturelle, 4th Series 8:257-265. . 1987. The systematic status of Australian Strongyloidea. Bulletin du Museum National d'Histoire Naturelle, 4th Series 9:107-126. , and J. H. Arundel. 1979. Helminth parasites of grey kangaroos, Macropus giganteus Shaw and M. fuliginosus (Desmarest) in Eastern Australia. Australian Wildlife Research 6:69-77. , P. J. A. Presidente, and R. Speare. 1985. Parasites and associated pathology of the swamp wallaby, Wallabia bicolor (Marsupialia). Journal of Wildlife Diseases 21:377-385. -, R. Speare, P. M. Johnson, and D. M. Spratt. 1992. Helminth parasite communities of macropodoid marsupials of the genera Hypsiprymnodon, Aepyprymnus, Thylogale, Onychogalea, Lagorchestes and Dendrolagus from Queensland. Wildlife Research 19:359-376. Johnston, T. H., and P. M. Mawson. 1939. Strongylate nematodes from marsupials in New South Wales. Proceedings of the Linnean Society of New South Wales 64:513-536. , and . 1940. Nematodes from South Australia marsupials. Transactions of the Royal Society of South Australia 64:95-100. Mawson, P. M. 1971. Pearson Island Expedition 1969. 8. Helminths. Transactions of the Royal Society of South Australia 95:169-183. . 1977. Revision of the genus Macropostrongylus and descriptions of three new genera: Popovastrongylus, Dorcopsinema andArundelia (Nematoda: Trichonematidae). Transactions of the Royal Society of South Australia 101:51-62. Smales, L. R. 1997. The status of Cyclostrongylus medioannulatus Johnston and Mawson, 1940. Transactions of the Royal Society of South Australia 121:165. , and P. M. Mawson. 1978. Nematode parasites of the Kangaroo Island Wallaby, Macropus eugenii (Desmarest). 1. Seasonal and geographic distribution. Transactions of the Royal Society of South Australia 102:9-16. Speare, R., I. Beveridge, P. M. Johnson, and L. A. Corner. 1983. Parasites of the agile wallaby Macropus agilis (Marsupialia). Australian Wildlife Research 10:89-96. Spratt, D. M., I. Beveridge, and E. L. Walter. 1991. A catalogue of Australasian monotremes and marsupials and their recorded helminth parasites. Records of the South Australian Museum, Monograph Series 1:1-105. Copyright © 2011, The Helminthological Society of Washington
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January 2000 Number 1 Comparative P
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Comp. Parasitol. 67(1). 2000 pp. 1-
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children. This means, to most of th
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liese, 1995; Marcogliese and Cone,
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Page 21 and 22: serve biodiversity effectively if e
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Page 37 and 38: COADY AND N]CKOL—PLAGIORHYNCHUS C
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Page 41 and 42: Threlfall, W. 1965. Helminth parasi
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Page 47 and 48: AMIN ET AL.—REVISION OF THE GENUS
Page 49 and 50: AMIN ET AL.—REVISION OF THE GENUS
Page 51 and 52: 17. Trunk spines appearing continuo
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Page 55 and 56: SMALES—POPOVASTRONGYLUS FROM MARS
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Page 59: strongylus pluteus differs from P.
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Page 65 and 66: Table 2. Parasite list for Onychoda
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Page 69 and 70: quadrant and 70° in male, 75° in
Page 71 and 72: increase in the number of cuticular
Page 75 and 76: Figures 1-3. Pseudoterranova decipi
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Page 79 and 80: the gill baskets of some hosts were
Page 81 and 82: KRITSKY ET AL.—DACTYLOGYRIDS FROM
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Page 93 and 94: MENDOZA-FRANCO ET M^.—SCIADICLEIT
Page 95 and 96: PEREZ-PONCE DE LEON ET AL.—DIGENE
Page 103 and 104: Table 2. Continued. Locality* (CNHE
Page 105 and 106: Table 2. Continued. Locality (CNHE
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Comp. Parasitol. 67(1), 2000 pp. 10
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Table 1. Extended. Ctenophorus reti
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Table 2. Extended. 3 '£ Oswaldofil
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Mediorhynchus orientalis Belopol'sk
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4-5 spines each: 25.0-35.0 (31.4).
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Table 1. Previous helminth records
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hyrae from a collection of lizards.
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WEST ET AL.—RESEARCH NOTES 123 Ta
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1987, and from these only a sample
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snakes are part of their diet. The
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Comp. Parasitol. 67(1), 2000 pp. 12
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Table 2. Published records of helmi
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, , B. K. Sullivan, and Q. A. Truon
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were larvae. Still, we have conclud
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and their habitats. These low paras
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e eligible for election to office.
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New business. Presentation of notes
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Name: MEMBERSHIP APPLICATION 143 AP
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*Edna M. Buhrer *Mildred A. Doss *A
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