The occurrence of gastrointestinal helminth parasites in 40 Macropus agilis, 12 M. antilopinus, 39 M. dorsalis, 28 M. giganteus, 29 M. parryi, 30 M. robustus and 26 Wallabia bicolor from north and central Queensland was examined. A total of 124 morphologically defined species of helminth was encountered, comprising 103 species of strongyloid nematodes, 6 species of trichostrongyloid nematodes, 2 species of spiruroid nematodes, 4 species of oxyuroid nematodes, 7 species of anoplocephalid cestodes and 2 species of digenetic trematodes. Helminth communities in each macropodid host species exhibited a high level of diversity, and were dominated numerically by strongyloid nematodes. A high proportion of the helminth species was restricted to a single host species and there was a low level of similarity between helminth communities in different host species. Similarities that did occur were not apparently related to the phylogenetic relationships between hosts and are best explained by host switching between hosts sharing overlapping habitats and feeding preferences. There was poor separation of the helminth species into ‘core’, ‘secondary’ and ‘satellite’ members of communities.

Nematodes, comprising 17 species, including 3 new genera, 4 new species and 3 putative new species, from the families Chabertiidae, Heligmonellidae, Herpetostrongylidae, Molineidae, Oxyuridae and Spiruridae were collected from the digestive tracts of 31 Paramelomys rubex (Murinae: Hydromyini) from Papua, Indonesia and Papua New Guinea. Mawsonema mokwanensis n. gen., n. sp. differs from all other genera in the Heligmonellidae in the characters of the synlophe, 15 ridges oriented sub frontally in the anterior body, the asymmetry of the bursa, the left lobe larger and the proportions of the dorsal ray. Melomystrongylus somoroensis n. sp. differs from its congener M. sepikensis in the number of ridges in the synlophe and the length of the spicules and female tail. A combination of the characters of the synlophe, 15 ridges oriented 55–60° from the saggital plane, lacking a carene, the asymmetry of the bursa and the proportions of the dorsal rays distinguishes Montistrongylus ingati n. gen., n. sp. from all other helligmonellids. Paraheligmosomoides singauwaensis is redescribed. It can be distinguished from P. amplicaudae n. sp., which has a similar number of synlophe ridges, but of differing proportions by the shape of the female tail and the proportions of the bursal lobes. Paraheligmosomoides ennisae n. sp. is characterized by the number of ridges of the synlophe, the shape of the female posterior end and the trilobed right spicule tip. Parasabanema n. gen., n. sp. differs from other heligmonellid genera in the arrangement and proportions of the 45 ridges and the left lateral dilatation of the synlophe. The herpetostrongylid Paraustrostrongylus paramelomysi n. sp. can be distinguished from its congenerics by a combination of characters including the number of synlophe ridges, the extent of the lateral floats in the female and the length of the proximally twisted spicules. Species richness of this nematode assemblage is similar to that of Melomys rufescens and Uromys caudimaculatus but species composition is not. Ten, including the three putative species, of the 17 species found in this study were unique to P. rubex. Biogeographic distributions within the helminth assemblage were discussed.

Adult and cystacanth forms of the acanthocephalan Serrasentis sagittifer from Australian coastal waters are redescribed and verified as the same species using both molecular and morphological data. This study provides the baseline 18S rDNA, 28S rDNA, and cox1 sequence data to serve as genetic barcode for S. sagittifer. The validity of the currently recognized species of Serrasentis is discussed. The most recently described species are junior synonyms of either Serrasentis nadakali or S. sagittifer, and a number of species are species inquirenda. When using morphological characters to distinguish the species of Serrasentis, consideration needs to be given to the maturity of the specimens, since the trunk elongates and the number and distribution of the ventral combs changes as worms mature, although the proboscis armature itself does not change. A simple key to assist in the identification of species of Serrasentis is provided. Adult S. sagittifer appear to be highly host specific to the cobia, Rachycentron canadum, in northern Australian waters, whereas cystacanths have been reported from a wide range of fish species. The relationship between host length and number of cystacanths shows that most paratenic infections are acquired as young fish, most likely via a crustacean intermediate host.

Parasites are ubiquitous in wild animals, with host-specific life histories considered as major determinants of prevalence and parasite assemblage patterns. It is predicted that habitat differences in logged rain forests influence population performances of small mammals and consequently may change the infection patterns of local animal populations with regard to endo-and ectoparasites. We investigated patterns of helminth species assemblages (Nematoda, Platyhelminthes) in two rat species (Leopoldamys sabanus, Niviventer cremoriventer) and two tree shrew species (Tupaia tana, T. longipes) in three logged and three unlogged rain forests in Borneo by examining 337 faecal samples with non-invasive faecal egg count (FEC). Nematode eggs prevailed in 9 5 % of all samples with up to five (mean 1.9 ± 1.1) morphotypes. Whereas members of Strongylida were most prevalent in L. sabanus, T. tana and T. longipes, Spirurida dominated in N. cremoriventer that revealed at the same time the lowest average nematode prevalence and FEC. Cestode eggs were only found in L. sabanus and T. tana. Composition and abundance patterns of the parasitic helminth assemblages were influenced by logging. As hypothesized, species richness of nematode morphotypes and mean number of infections per host of T. longipes were larger in logged than in unlogged forest. In contrast, L. sabanus was more heavily infected with cestodes in unlogged than in logged forest and also revealed larger egg counts for strongylids and spirurids in unlogged forest. Our results suggest that forest degradation and altered environmental conditions influence helminth diversity and infection patterns of small mammals with contrasting trends among host species. The inconsistent logging-induced changes in helminth assemblages from different hosts indicate that specific sets of habitat-host-parasite interactions are uniquely influenced by the effects of logging. Consequently, predictions on changes of parasite diversity and prevalence with regard to habitat disturbance need to be based on the individual life histories of the hosts (and the parasites).

Two new species of Andracantha (Polymorphidae) are described from the intestine of the shags Leucocarbo chalconotus (Gray) and Phalacrocorax punctatus (Sparrman), and the penguin Eudyptula minor (Forster) from southern South Island, New Zealand. Andracantha leucocarboi n. sp. is distinguished from its congeners by having no genital or ventral trunk spines, but possessing a scattering of small spines between the anterior fields of spines. This is the first record of a species of Andracantha from a penguin. Circumbursal papillae are illustrated in a scanning electron micrograph for the first time in the polymorphids. Andracantha sigma n. sp. is distinguished by the sigmoid shape of its largest proboscis hook, hook VIII, and having the ventral field separated from the posterior disc field by an aspinous gap. A Maximum Likelihood tree from cox1 and large ribosomal subunit (LSU) data shows A. leucocarboi n. sp. to be more closely related to A. gravida than A. sigma n. sp. and the genus Andracantha as sister to Corynosoma spp. Genetic distances between species of Andracantha are comparatively large. A key to the species of Andracantha is provided.

In a survey of 1,732 amphibians and reptiles collected across São Paulo Province, Brazil, and 7 provinces in Paraguay, 26 species were found infected with acanthocephalans. Of 1,510 anurans, 14 anurans, representing 11 species, were infected with cystacanths of Centrorhynchus spp. and 1 anuran with cystacanths of Oligacanthorhynchus sp. Of 107 lizards, 1 lizard was infected with cystacanths of Centrorhynchus sp. and 1 lizard with cystacanths of Oligacanthorhynchus sp. Acanthocephalus caspanensis was found in 3 anurans (3 species) and Acanthocephalus lutzi in 3 anurans (2 species) and 2 snakes (2 species). The systematic position of A. lutzi cannot be resolved using presently available morphological data. Acanthocephalus saopaulensis n. sp. was found in a single individual of Bufo ictericus. The new species can be differentiated from all its congeners except A. caspanensis in having a sigmoid-shaped male posterior end and from A. caspanensis in having a proboscis armature of 16 rows of 5-7 hooks rather than 18-19 rows of 6-7 hooks and larger eggs. The status of Acanthocephalus and Pseudoacanthocephalus continues to be problematic.

This study documents the helminth assemblages of Uromys caudimaculatus (Krefft, 1867) from Papua New Guinea and Australia as well as listing helminths found in U. anak Thomas, 1907 from Papua Indonesia and Papua New Guinea, and U. hadrourus (Winter, 1984) from Queensland Australia. In total, 36 species of helminth, comprising one acanthocephalan, three cestodes (excluding unidentifiable fragments) and 32 nematodes (including two not identified to genus) from 65 hosts were found. The Trichostrongylina nematodes were the dominant group of helminths, the most prevalent species being Odilia uromyos (Mawson, 1961), found in each of the species of Uromys across all regions, and O. melomyos (Mawson, 1961), occurring in U. caudimaculatus from Papua New Guinea and Australia. The helminth species assemblage from U. caudimaculatus, 14 species of helminth from 11 hosts from Papua New Guinea and 23 species of helminth from 51 hosts from Australia, had high species richness but was relatively equitable overall (1/SI = 0.92). The differences found between the helminth assemblages of U. caudimaculatus from Papua New Guinea and Australia suggest that U. caudimaculatus may have travelled to Australia from New Guinea with a small pool of helminth species that was subsequently added to by host switching from sympatric rodent hosts. Alternatively, U. caudimaculatus may have lost many of the helminths that travelled with it following arrival in Australia.

Profilicollis novaezelandensis n. sp. (Acanthocephala: Polymorphidae) is described from the South Island pied oystercatcher Haematopus ostralegus finschi Martens (Haematopodidae) and the intertidal crab Hemigrapsus crenulatus (Milne Edwards) (Brachyura: Grapsidae) from the South Island of New Zealand. The new species can be distinguished from all the other species of the genus by a combination of the following characters: long neck (13% of total body length for adults) and a subspherical proboscis with 14-16 longitudinal rows of 7-8 hooks. The mud crabs Helice crassa Dana (Grapsidae) and Macrophthalmus hirtipes (Heller) (Ocypodidae) were also harbouring cystacanths and the bar-tailed godwit Limosa lapponica (Linnaeus) (Scolopacidae) juveniles of P. novaezelandensis. This is the first record of brachyuran decapods as intermediate hosts of Acanthocephala from New Zealand. P. antarcticus is recorded from three crab species (Helice crassa, Hemigraspus crenulatus and Macrophthalmus hirtipes) and two bird species (Haematopus o. finschi and Limosa lapponica) in New Zealand. An unidentified species of Plagiorhynchus was also found in two bird species (H. o. finschi and H. unicolor Forster). P. antarcticus and P. novaezelandensis are the first records of Profilicollis from New Zealand.