Two New Species of the Genus Heterakis (Heterakidae) from the Genera Echymipera, Isoodon and Perameles (Peramelidae), Bandicoots from Papua New Guinea and Australia.

PURPOSE: To identify and describe any new nematode species of the genus Heterakis Dujardin, 1845 (Heterakidae Railliet & Henry, 1914) found in bandicoots (Peramelidae Gray, 1825) collected from Australia and Papua New Guinea and held in the South Australian Museum, Adelaide. METHODS: All the relevant specimens registered in the South Australian Museum were examined as temporary wet mounts, after clearing in lactophenol, using an Olympus BH-2 microscope with differential interference optics. Measurements were made with an eyepiece micrometer and figures drawn using a drawing tube. RESULTS: Heterakis balamukensis n. sp. was described from Echymipera kabulu (Lesson, 1828) collected from Balamuk station, Bensbach River, Papua New Guinea and Heterakis oweni n. sp. was described from Isoodon macrourus (Gould, 1842) collected from Papua New Guinea, and Queensland, Australia. Heterakis sp. females were identified from I. macrourus from the Northern Territory and Perameles pallescens Thomas, 1923 from Queensland, Australia. A key to the valid species of Heterakis from mammals is given. CONCLUSIONS: The heterakid fauna of mammals now comprises eight species: the cosmopolitan species Heterakis spumosa Schneider, 1886 as well as H. balamukensis n. sp., H. fieldingi Smales, 1996, H. oweni n. sp. and H. sirawii Smales, 2016 from Australasia, H. dahomensis (Gendre, 1911) from Africa, and H. inglisi Gupta & Trevadi, 1982 and H. yamagutii Gupta & Trevadi, 1982 from India. Two species have been declared species inquirenda; H. equispicularis Uphadyyay, 2017 and H. verrucosa Molin, 1860, while H. rattui Ghambir, Gyaneswori, Tarnita, Indrani & Zenith, 2008 falls as a junior synonym of H. spumosa. No infections of the cosmopolitan species infecting rodent hosts, Heterakis spumosa Schneider, 1866, were found in bandicoots.

An Evaluation of the Genera Longicollum and Paralongicollum (Pomphorhynchidae: Acanthocephala) in Australia.

PURPOSE: To confirm the identity of Longicollum edmondsi Golvan, 1969, Pomphorhynchidae Yamaguti, 1939, from Australia. METHODS: All the relevant specimens registered in Australian museums were examined. Those held as permanent slide preparations were examined directly and those stored in 70% ethanol were examined as temporary wet mounts, after clearing in lactophenol, using an Olympus BH-2 microscope with differential interference optics. Measurements were made with an eyepiece micrometer and figures drawn using a drawing tube. RESULTS: All the material registered as either Longicollum edmondsi or Paralongicollum sp. was determined to be Paralongicollum edmondsi (Golvan, 1969) comb. nov. based, amongst other characters, on the morphology of the neck. DISCUSSION: The significance of known host species of P. edmondsi and their geographical distribution around the Australian coast was analysed. The geographical distribution of the genus Paralongicollum, Amin, Bauer & Siderov, 1991, across the Indo Pacific was compared to that of the acanthocephalan genus Sclerocollum Schmidt & Paperna, 1978.

Molecular characterisation and updated description of Neoechinorhynchus aldrichettae Edmonds, 1971 (Acanthocephala: Neoechinorhynchidae), based on material from Aldrichetta forsteri (Valenciennes) collected in Tasmania, Australia.

We report on Neoechinorhynchus aldrichettae Edmonds, 1971 (Acanthocephala: Neoechinorhynchidae), obtained from yellow-eye mullet Aldrichetta forsteri (Valenciennes) (Mugiliformes: Mugilidae) from the Huon River, Tasmania, Australia. We provide new 18S and 28S rDNA gene sequence data for N. aldrichettae, assess its phylogenetic position relative to other species of Neoechinorhynchus and provide an updated morphological account of this species including detail of features omitted in the type-description, specifically of the apical organ, a collar at the base of the neck and a para-receptacle structure associated with the proboscis receptacle. We determine that eggs in this species are ovoid, without polar prolongations of fertilisation membrane, which permits assignment of N. aldrichettae to the subgenus Neoechinorhynchus. Our phylogenetic analyses place N. (N.) aldrichettae in a clade with other species of Neoechinorhynchus which parasitise mullets in marine and estuarine waters. We find that, in terms of monophyletic clades, the current subgeneric classification system for Neoechinorhynchus is not reflected in our phylogenetic analyses.

Gorgorhynchoides pseudocarangis n. sp. (Acanthocephala: Isthmosacanthidae) from Pseudocaranx dentex (Carangidae) in southeast Queensland, Australia, with comments on the Isthmosacanthidae.

Gorgorhynchoides pseudocarangis n. sp. (Isthmosacanthidae), is described from the intestine of the white trevally Pseudocaranx dentex (Bloch & Schneider) (Carangiformes: Carangidae) collected in Moreton Bay, Queensland, Australia. The new species has a proboscis armature of 27-28 rows of 16-17 hooks. It is most similar morphologically to Gorgorhynchoides bullocki Cable & Marafachisi, 1970 and Gorgorhynchoides gnathanodontos Smales, 2014 but differs from the former in having a longer proboscis with more rows of hooks, ventral hooks 6/7-12 with notched tips and trunk spines which do not extend onto the anterior bulbous swelling, and from the latter in having a longer proboscis, ventral hooks 6/7-12 with notched tips, more circles of trunk spines, larger eggs and a proboscis armature with all hooks lacking manubria. Previous molecular phylogenetic analyses have shown that the genus Serrasentis Van Cleave, 1923 is sister to Gorgorhynchoides Cable & Linderoth, 1963, although some have failed to resolve these two lineages in separate monophyletic clades. We performed novel single-gene and concatenated phylogenetic analyses using cox1 mtDNA, 18S and 28S rDNA gene-sequences, resolving Gorgorhynchoides and Serrasentis in monophyletic sister clades and demonstrating that Gorgorhynchoides pseudocarangis n. sp. is phylogenetically distinct from related species for which molecular sequence data are available. We view the previous amendment of the Isthmosacanthidae to include the genera Golvanorhynchus Noronha, Fabio & Pinto, 1987, Gorgorhynchoides, Isthmosacanthus Smales 2014 and Serrasentis, and the transfer of the family to the Polymorphida, as the most satisfactory classification at present, although additional molecular evidence would provide greater stability.

Correction to: Molecular characterisation of acanthocephalans from Australian marine teleosts: proposal of a new family, synonymy of another and transfer of taxa between orders.

Shortly after publication it was brought to authors' attention that two of the cox1 sequences reported in the study, those of Neoechinorhynchus tylosuri (MN692675) and Transvena annulospinosa (MN692690) were potentially erroneous. After investigation, it was determined that this was indeed the case and was caused by contamination of original sequencing results. They were found to be near-duplicates of other species from the same sequencing batch. These sequences have been removed from GenBank. Unfortunately, this means that no cox1 sequence data were provided for the above two species in the referenced study. The remaining cox1 sequences reported have been checked and are reliable. Furthermore, cox1 sequence data were not analysed as part of the study, and thus the above error does not affect the results or conclusions of the study. Corrections to the text in reference to the above are made in Table 1 (removal of the above GenBank accession numbers), on page 10 ("Sequence data for all three targeted markers were obtained for 13 (rather than 15) of the 17 acanthocephalan species studied") and on page 19 ("We generated new cox1 sequence data for all but three (rather than one) of the acanthocephalan species from our collection…").

Proposal of Spinulacorpus biforme (Smales, 2014) n. g., n. comb. and the Spinulacorpidae n. fam. to resolve paraphyly of the acanthocephalan family Rhadinorhynchidae Lühe, 1912.

Previous phylogenetic analyses of the Acanthocephala have demonstrated that the families Rhadinorhynchidae Lühe, 1912 and Transvenidae Pichelin & Cribb, 2001 are sister clades. However, a recent study found that the Rhadinorhynchidae is paraphyletic, due to the basal position of Rhadinorhynchus biformis Smales, 2014 relative to the Rhadinorhynchidae + Transvenidae. We reassess these relationships with new single-gene and concatenated phylogenetic analyses utilising cox1 mtDNA, 18S rDNA and 28S rDNA, including recently available sequences. Although topologies differed among single-gene analyses, the overall results support R. biformis as representative of a lineage distinct from those of the Rhadinorhynchidae and Transvenidae. Examination of additional specimens of R. biformis allowed us to identify morphological characters that further support this hypothesis. These results lead us to propose transfer of R. biformis to a new genus (Spinulacorpus n. g.) and family (Spinulacorpidae n. fam.) to resolve the paraphyly of the Rhadinorhynchidae.

Morphological and molecular characterisation of a new genus and species of acanthocephalan, Tenuisoma tarapungi n. g., n. sp. (Acanthocephala: Polymorphidae) infecting red-billed gulls in New Zealand, with a key to the genera of the Polymorphidae Meyer, 1931.

Acanthocephalans of the family Polymorphidae Meyer, 1931 are cosmopolitan parasites that infect the intestines of fish-eating birds and mammals. Polymorphid acanthocephalans recovered from the intestines of red-billed gulls (Chroicocephalus scopulinus (Forster)) from the Otago coast, New Zealand, although morphologically similar to the genus Arhythmorhynchus Lühe, 1911 nevertheless have a unique molecular profile showing considerable genetic differentation, and are here diagnosed and described as Tenuisoma tarapungi n. g., n. sp. Characters which distinguish T. tarapungi include a very elongate, cylindrical hindtrunk, swollen anterior trunk with a spinose region, a secondary swelling in males only containing the testes, and hypodermal nuclei distributed throughout the length of the trunk. Molecular data (cox1, 18S, 28S) confirm that the representative of the new genus is closest to, but nonetheless strongly divergent from species of Pseudocorynosoma Aznar, Pérez-Ponce de León & Raga, 2006. Immature specimens are described and illustrated, demonstrating the extreme degree of hindtrunk inversion occurring in immature individuals of this species. We provide a key to the genera of the family Polymorphidae.

Molecular characterisation of acanthocephalans from Australian marine teleosts: proposal of a new family, synonymy of another and transfer of taxa between orders.

We provide molecular data (cox1, 18S rDNA and 28S rDNA) for 17 acanthocephalan species and 20 host-parasite combinations from Australian marine teleosts collected from off Queensland, Australia. Fourteen of these acanthocephalans are characterised with molecular data for the first time and we provide the first molecular data for a species of each of the genera Heterosentis Van Cleave, 1931, Pyriproboscis Amin, Abdullah & Mhaisen, 2003 and Sclerocollum Schmidt & Paperna, 1978. Using 18S and 28S rDNA sequences, the phylogenetic position of each newly sequenced species is assessed with both single-gene and concatenated 18S+28S maximum likelihood and Bayesian inference analyses. Additional phylogenetic analyses focusing on the genus Rhadinorhynchus Lühe, 1912 and related lineages are included. Our phylogenetic results are broadly consistent with previous analyses, recovering previously identified inconsistencies but also providing new insights and necessitating taxonomic action. We do not find sufficient evidence to recognise the Gymnorhadinorhynchidae Braicovich, Lanfranchi, Farber, Marvaldi, Luque & Timi, 2014 as distinct from the Rhadinorhynchidae Lühe, 1912. The family Gymnorhadinorhynchidae and its sole genus, Gymnorhadinorhynchus Braicovich, Lanfranchi, Farber, Marvaldi, Luque & Timi, 2014, are here recognised as junior synonyms of Rhadinorhynchidae and Rhadinorhynchus, respectively. The two species currently assigned to Gymnorhadinorhynchus are recombined as Rhadinorhynchus decapteri (Braicovich, Lanfranchi, Farber, Marvaldi, Luque & Timi, 2014) n. comb. and Rhadinorhynchus mariserpentis (Steinauer, Garcia-Vedrenne, Weinstein & Kuris, 2019) n. comb. In all of our analyses, Rhadinorhynchus biformis Smales, 2014 is found basal to the Rhadinorhynchidae + Transvenidae Pichelin & Cribb, 2001, thus resulting in a paraphyletic Rhadinorhynchidae. It appears that R. biformis may require a new genus and family; however, morphological data for this species are currently insufficient to adequately distinguish it from related lineages, thus we defer the proposal of any new higher-rank names for this species. Species of the genus Sclerocollum, currently assigned to the Cavisomidae Meyer, 1932, are found nested within the family Transvenidae. We transfer the genus Sclerocollum to the Transvenidae and amend the diagnosis of the family accordingly. The genera Gorgorhynchoides Cable & Linderoth, 1963 and Serrasentis Van Cleave, 1923, currently assigned to the Rhadinorhynchidae, are supported as sister taxa and form a clade in the Polymorphida. We transfer these genera and Golvanorhynchus Noronha, Fabio & Pinto, 1978 to an emended concept of the Isthomosacanthidae Smales, 2012 and transfer this family to the Polymorphida. Lastly, Pyriproboscis heronensis (Pichelin, 1997) Amin, Abdullah & Mhaisen, 2003, currently assigned to the Pomphorhynchidae Yamaguti, 1939, falls under the Polymorphida in our analyses with some support for a sister relationship with the Centrorhynchidae Van Cleave, 1916. As this species clearly does not belong in the Pomphorhynchidae and is morphologically and molecularly distinct from the lineages of the Polymorphida, we propose the Pyriprobosicidae n. fam. to accommodate it.

Description of New Species of Coronostrongylus and Dorcopsistrongylus (Strongylida: Chabertiidae) from Dorcopsis muelleri (Macropodidae) from Kumawa Mountains, West Papua, Indonesia.

New species of Coronostrongylus and Dorcopsistrongylus (Strongyloidea: Chabertiidae) are described from Dorcopsis muelleri (Macropodidae) from Kumawa Mountains, West Papua, Indonesia. Coronostrongylus hasegawai n.sp .is most similar to C. spearei, the only other species described from New Guinea, in having 24 longitudinal pleats in the buccal cavity and spicules less than 1,400 long. Coronostrongylus hasegawai differs from C. spearei, in a suite of characters including the shape of the cephalic collar, the proportions of the buccal capsule, the disposition of the bursal rays, the length of the spicules and the proportions of the ovejector. Dorcopsistrongylus supriyatnai n.sp differs from all congeners in lacking large anteriorly directed intestinal diverticula. The genus Coronostrongylus is found in Australia and New Guinea while the genus Dorcopsistrongylus appears to be endemic to New Guinea.

Acanthocephalans from Australian elasmobranchs (Chondrichthyes) with a description of a new species in the genus Gorgorhynchus Chandler, 1934 (Rhadinorhynchidae).

Gorgorhynchus occultus n. sp. is described from Sutorectus tentaculatus (Peters) (Orectolobidae) collected off Bunbury, Western Australia in 1986. The new species differs from all other species of Gorgorhynchus Chandler, 1934 by having a suite of characters including a proboscis hook formula of 18-20 rows of 8-9 hooks, a well-developed neck, irregular circles of small spines in a single anterior field, the male reproductive system limited to the posterior quarter of the trunk and three cement glands. In a survey of 284 sharks collected between 2015 and 2018 from 10 localities in Australian waters, 11 individuals were infected with acanthocephalan cystacanths. One individual of Sphyrna mokarran (Rupell) (Sphyrnidae) was infected with Corynosoma cetaceum Johnston & Best, 1931. Serrasentis sagittifer (Linton, 1889) (Rhadinorhynchidae) was found in five individuals of S. mokarran, four individuals of Syphyrna lewini (Griffith & Smith) and one individual of Carcharhinus coatesi (Whitley) (Carcharhinidae). These infections may be accidental because it has been suggested that acanthocephalans cannot tolerate the high levels of urea used by marine and esturine elasmobranchs for osmoregulation. The two most common host species examined, S. mokarran and S. lewini had the highest intensities and prevalences of infection with S. sagittifer. Although more individuals of S. lewini were examined, S. mokarran had the higher prevalence of infection.

Morphological and molecular evidence for synonymy of Corynosoma obtuscens Lincicome, 1943 with Corynosoma australe Johnston, 1937 (Acanthocephala: Polymorphidae).

Corynosoma obtuscens Lincicome, 1943 (Acanthocephala: Polymorphidae) is synonymised with Corynosoma australe Johnston, 1937 based on combined morphological and molecular evidence. Morphological comparison of C. obtuscens (24 males and 27 females) collected from a California sea lion Zalophus californianus (Lesson) in California, USA, with the type-specimens of C. obtuscens and C. australe, and with published data on C. australe collected from different hosts and regions showed no significant differences. The levels of genetic divergence in the cox1 sequences obtained from C. obtuscens from a California sea lion in the present study and C. australe from otariid seals from Argentina and penguins from Brazil ranged between 1.4-1.6% and was considered to represent intraspecific variability. Additionally, cox1 sequences were generated for Andracantha phalacrocoracis (Yamaguti, 1939), Corynosoma semerme (Forssell, 1904), C. strumosum (Rudolphi, 1802), C. validum Van Cleave, 1953 and C. villosum Van Cleave, 1953. Our results revealed inconsistency in the identification of material used as a source of the previously published sequence data for C. obtuscens and C. magdaleni Montreuil, 1958.

Checklist of acanthocephalan parasites of South Africa.

Twenty-one species of acanthocephalans, representative of thirteen genera from ten families of seven orders and three classes, are included in this updated checklist of acanthocephalans in South Africa. Although South Africa appears to have a less diverse acanthocephalan fauna compared to some other countries such as Iran in Asia, or Brazil in South America, this is probably an artefact of fewer parasitological surveys.

Redescription of Maupasina weissi (Seurat, 1913) (Nematoda: Ascaridida) from sengis, Elephantulus spp. and Macroscelides proboscideus (Shaw) (Macroscelidea), in Africa.

Maupasina weissi (Seurat, 1913), is redescribed from the eastern rock sengi, Elephantulus myurus Thomas & Schwann, from Limpopo Province and compared with material collected from Free State and North West Provinces, South Africa, as well as the description of the type-material from South Tunisia. Distinguishing features of the species include a corona radiata of 12 pointed leaflike elements, a complex bipartite buccal capsule with 3 large bicuspid denticular lobes and 4 smaller club-shaped lobes and 11 (occasionally 10) pairs of cloacal papillae in the male. The complex taxonomic history of the genus Maupasina Seurat, 1917 is discussed. The probable misidentification of Macroscelides proboscideus Shaw, the short eared sengi, from North West Province, South Africa, as a host of M. weissi is explained, indicating that M. weissi occurs only in species of the genus Elephantulus Thomas & Schwann. The widely separated geographical regions, stretching the length of the African continent, in which M. weissi has been found are indicative of a conservative species with a broad geographical distribution. Tenebrionid beetles, up to 50% of stomach contents of E. myurus in Limpopo Province may act as intermediate hosts in the life-cycle of M. weissi.

The gastrointestinal nematodes of Paramelomys lorentzii and Mammelomys spp. (Rodentia: Muridae) with descriptions of a new genus and three new species (Heligmonellidae) from Papua New Guinea and Indonesia.

Unidentified cestodes and 14 species of nematode and larvae that could not be placed to family level, were collected from the digestive tracts of 27 individuals of Paramelomys lorentzii, four of Mammelomys lanosus and a single M. rattoides from Papua New Guinea and Papua Indonesia. Of these three were new species. Hughjonestrongylus woolleyae sp. nov. can be distinguished from its congeners in having up to 26 ridges in the synlophe and a dissymmetric dorsal ray. Parvinema bafunminensis gen. nov., sp. nov. can be distinguished from all other genera in the family by the combination of features in the synlophe; with a carene, up to 17 ridges, and the pattern of ridge sizes. Parvinema helgeni sp. nov. differs from P. bafunminensis in the length of the spicule and the number of eggs in the uterus. The nematode assemblage of P. lorentzii had similar species richness to, and was also dominated by heligmonellids, as that of Paramelomys rubex, although the two assemblages differed in species composition.

A new species of Centrorhynchus Lühe, 1911 (Acanthocephala: Centrorhynchidae) from the lizard buzzard Kaupifalco monogrammicus (Temminck) (Aves: Accipitridae) in South Africa.

Centrorhynchus sarehae n. sp. is described from the lizard buzzard Kaupifalco monogrammicus (Temminik) in Louis Trichardt City, Limpopo Province, South Africa. The new species can be distinguished from all other species of Centrorhynchus Lühe, 1911 except C. gendrei (Golvan, 1957) and C. mariauxi Smales, 2011 in having a dilated region in the posterior trunk of the female. Centrorhynchus sarehae differs from both these species in the characters of the proboscis armature, particularly the number of hooks per row and the lengths of the longest hooks. This is the first record of a fully identified species of Centrorhynchus in South Africa.

Novel morphological and molecular data for Corynosoma hannae Zdzitowiecki, 1984 (Acanthocephala: Polymorphidae) from teleosts, fish-eating birds and pinnipeds from New Zealand.

The polymorphid acanthocephalan, Corynosoma hannae Zdzitowiecki, 1984 is characterised on the basis of newly collected material from a New Zealand sea lion, Phocarctos hookeri (Gray), and long-nosed fur seal, Arctophoca forsteri (Lesson) (definitive hosts), and from Stewart Island shags, Leucocarbo chalconotus (Gray), spotted shags, Phalacrocorax punctatus (Sparrman) and yellow-eyed penguins, Megadyptes antipodes (Hombron & Jacquinot) (non-definitive hosts) from New Zealand. Specimens are described in detail and scanning electron micrographs for C. hannae are provided. Additionally, cystacanths of C. hannae are reported and described for the first time from the body cavity and mesenteries of New Zealand brill, Colistium guntheri (Hutton) and from New Zealand sole, Peltorhamphus novaezeelandiae Günther from Kaka Point, Otago in New Zealand. Partial sequence data for the mitochondrial cytochrome c oxidase 1 gene (cox1) for adults, immature specimens and cystacanths of C. hannae were obtained. Phylogenetic analyses of the newly-generated sequences and for available cox1 sequences of Corynosoma spp. revealed a close relationship between C. hannae and C. australe Johnston, 1937, both species infecting pinnipeds in the Southern Hemisphere. However, a morphological comparison of the species suggests that C. hannae mostly closely resembles C. evae Zdzitowiecki, 1984 and C. semerme (Forssell, 1904), the latter of which occurs in pinnipeds in the Northern Hemisphere.

A review of the genus Sclerocollum Schmidt & Paperna, 1978 (Acanthocephala: Cavisomidae) from rabbitfishes (Siganidae) in the Indian and Pacific Oceans.

Seven of the eleven species of Siganus Richardson (Siganidae) collected off the coasts of Australia, New Caledonia, French Polynesia and Palau were infected with species of Sclerocollum Schmidt & Paperna, 1978 (Acanthocephala: Cavisomidae). A Principal Component Analysis (PCA) and a Discriminant Analysis were performed on a morphometric dataset of specimens of Sclerocollum including borrowed type-specimens of Sc. rubrimaris Schmidt & Paperna, 1978 from the Indian Ocean and of Sc. robustum Edmonds, 1964, the only acanthocephalan species known previously from an Australian siganid. These analyses showed that the lengths of proboscis hooks were useful variables for separating specimens into groups and supported the presence of two known species (Sc. robustum and Sc. rubrimaris) and one new species (Sc. australis n. sp.) in Australian waters. We found Sc. robustum in Siganus lineatus (Valenciennes) from off Queensland and Sc. rubrimaris in S. fuscescens (Houttuyn) from off Western Australia and Queensland, S. punctatissimus Fowler & Bean from off Queensland and S. argenteus (Quoy & Gaimard), S. corallinus (Valenciennes), S. canaliculatus (Park) and S. doliatus Guérin-Méneville from off New Caledonia (all new host and locality records) which we compared with museum specimens of Sc. rubrimaris from S. rivulatus Forsskål & Niebuhr and S. argenteus [as S. rostratus (Valenciennes)] from the Red Sea. The third species, Sclerocollum australis n. sp., was found only in S. corallinus and S. doliatus from off Queensland. Sclerocollum australis n. sp. can be distinguished from its congeners by a unique combination of characters of the proboscis armature, including lengths of hooks 1-7. Specimens of Sclerocollum were also found in Zebrasoma velifer (Bloch) (Acanthuridae) from off Queensland, and Coradion altivelis McCulloch (Chaetodontidae) and Heniochus acuminatus (Linnaeus) (Chaetodontidae) from off New Caledonia. No acanthocephalans were found in siganids collected from Palau (Micronesia) or Moorea (French Polynesia) or Moreton Bay and Noosa (Queensland, Australia). We found no acanthocephalans in S. puellus (Schlegel), S. punctatus (Schneider & Forster), S. spinus (Linnaeus) or S. vulpinus (Schlegel & Müller). Evidence suggests that species of the genus Sclerocollum have travelled with S. argenteus across the Indo-Pacific with Sc. rubrimaris dispersed widely and Sc. robustum and Sc. australis n. sp. restricted to the Queensland coast, Australia.

Nematodes of Heligmonellidae (Strongylida) of Pogonomys championi Flannery and Pogonomys sylvestris Thomas (Rodentia: Muridae) from Papua New Guinea with descriptions of five new species.

Eight species of heligmonellid nematodes including five new species and a putative new species were identified from the digestive tracts of 12 Pogonomys championi Flannery and 27 P. sylvestris Thomas (Murinae: Hydromyini) from Papua Indonesia. Hasanuddinia pogonomyos Smales, 2014 had been previously described from P. loriae Thomas and P. macrourus (Milne-Edwards) and Odilia mackerrasae (Mawson, 1961) from several endemic rodent species. Bunomystrongylus ilami n. sp. can be distinguished from its congeners by the number of rounded ridges in the synlophe; Hasanuddinia hasegawai n. sp. by the number of ridges, three ventral being hypertrophied, in the synlophe; Montistrongylus kaindiensis n. sp. by the number of ridges in the synlophe and the length of the spicules; Odilia helgeni n. sp. in the characters of the synlophe ridges; Odilia whittingtoni n. sp. in the characters of the synlophe ridges and the length of the spicules. Species richness of the nematode assemblage of P. sylvestris, nine species and a juvenile heligmonellid, was comparable to those of P. loriae and P. macrourus but that of P. championi, five species, was considered depauperate. Species composition showed both commonalities between the host species as well as distinctive features. Three of five species in the assemblage were unique to P. championi and five of nine species to P. sylvestris.

An annotated checklist of Acanthocephala from Australian fish.

Thirty one genera, comprising 58 named species, 15 undetermined species and nine species known only as cystacanths from paratenic fish hosts were found infesting 144 marine, esturine and freshwater species of fish from Australian and Australian Antarctic waters. Host habitats are given and the distribution and records of the acanthocephalans are given. A key to these parasites at the generic level is provided.