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Relationships between the strongyloid nematodesRugopharynx delta, R. zeta, R. omega, R. longibursaris, R. mawsonae andR. sigma, all from macropodid marsupials, were investigated using allozyme data. The phylogenetic trees derived from the electrophoretic data set were congruent with those of the hosts and were consistent with the hypothesis that the species complex originated in pademelons of the genusThylogale and diversified in rock-wallabies (Petrogale spp.) and scrub wallabies of the subgenusNotamacropus. Host switching is evident only between closely related macropodid taxa.

An electrophoretic study was conducted on nematodes of the genus Physaloptera that occur in the stomachs of two species of Australian bandicoot, Perameles nasuta and P. gunnii. Each nematode was genetically characterised at 28 enzymes encoding a presumptive 30 loci. No fixed genetic differences were detected between the nematodes in P. gunnii from two localities. A comparison of nematodes from the two host species, however, revealed fixed genetic differences at 15 (50%) loci. This suggests that each host species is infected by a different species of Physaloptera.

Rugopharynx zeta (Johnston & Mawson) (Nematoda: Strongyloidea) is redescribed from the rock wallabies Petrogale penicillata penicillata, P. p. herberti, P. inornata and P. assimilis from Queensland and New South Wales, Australia. Specimens formerly assigned to this nematode taxon from the wallabies Macropus dorsalis and M. parma are treated as a new species, R. mawsonae. R. mawsonae n. sp. differs from R. zeta in the shape of the dorsal ray, length of spicules, morphology of spicule tip, length of female tail and position of deirid. The morphological differences are supported by electrophoretic data. R. zeta and R. mawsonae n. sp. had fixed genetic differences at 45.0% of the 21 enzyme loci examined, while each differed at 38.1% and 45.0% of loci respectively from the morphologically distinct R. delta (Johnston & Mawson). The known host and geographical distributions of R. zeta and R. mawsonae n. sp. are reviewed.

An electrophoretic comparison of the nematodes Rugopharynx longibursaris and R. omega, both from Macropus rufogriseus in south-eastern Australia, revealed fixed genetic differences at 4.5% of the 23 enzyme loci examined. The electrophoretic data do not therefore reject the null hypothesis that the two taxa are conspecific. R. longibursaris was found in Tasmania and in the western mainland population of M. rufogriseus, while R. omega occurred only in the eastern mainland population. Implications for the taxonomic status of the western host population are considered. Specimens formerly assigned to R. omega, from Thylogale stigmatica from Queensland, were found to differ at 45.0% of enzyme loci from specimens from M. rufogriseus. Morphological examination revealed differences in the shape of the buccal capsule, the position of the deirid, the morphology of the spicule tip and the presence of a gubernaculum. A new species, R. sigma, is erected for specimens from T. stigmatica, T. thetis and T. calabyi.

An allozyme study of four populations of Paramacropostrongylus typicus from Macropus fuliginosus and M. giganteus detected the presence of a distinct species, Paramacropostrongylus iugalis n. sp., which is described from the stomach of the eastern grey kangaroo Macropus giganteus. The description is based on samples possessing fixed allelic differences at 10 of 37 enzyme loci examined, minor morphological differences from its congener P. typicus in M. fuliginosus, and presumed limitation to a single host species, M. giganteus. Its differentiation from P. typicus is more clearly demonstrated by biochemical characters than by morphological ones. The two parasite species probably co-speciated with their hosts.

An electrophoretic analysis using 17 enzyme loci was carried out on specimens of the gastric nematode of macropodid marsupials, Rugopharynx australis (Monnig, 1926), collected from Macropus eugenii (Desmarest), M. fuliginosus (Desmarest), M. giganteus Shaw, M. robustus Gould, M. rufogriseus (Desmarest), M. rufus (Desmarest), Thylogale billardierii (Desmarest) and Wallabia bicolor (Desmarest) from south-eastern Australia. The extent of fixed genetic differences between nematodes from different host species ranged from 0–53%. The two distinct morphological forms of the parasite found in M. rufogriseus differed at 50% of loci. Specimens present in M. fuliginosus and M. giganteus were indistinguishable genetically, as were nematodes from M. rufus and M. robustus. Of the two morphologically distinct congeners included in the analysis as controls, Rugopharynx epsilon (Johnston & Mawson, 1939) was genetically distinct (46–69% fixed genetic differences) from all specimens of the R. australis complex while R. rufogrisea Magzoub, 1964 was closely related to one of the two species occuring in M. rufogriseus. It was concluded that R. australis is a species complex, with a genetically distinct species present in M. eugenii, M. fuliginosus/M. giganteus, M. robustus/M. rufus, W. bicolor and T. billardierii, and two species in M. rufogriseus.

Macropostrongyloides baylisi from four different species or subspecies of host were analysed electrophoretically at 27 enzyme loci. The results revealed the existence of two species, one in Macropus giganteus and the other in M. robustus robustus, M.r. erubescens and M.r. parryi, that had fixed genetic differences at 33% of loci. Populations of nematodes from two subspecies of M. robustus, M.r. robustus from Queensland and M.r. erubescens from South Australia, had fixed genetic differences at two (7.4%) of 27 loci and were considered to belong to the same species. No fixed genetic differences were detected between nematodes from M. parryi and M.r. robustus. A discriminant function analysis of morphological data assigned 96% of specimens to groups defined on the basis of the host species or subspecies from which they were obtained. This separation of Ma. baylisi into host-specific groups did not, however, totally correlate with the electrophoretic data. The species of M. baylisi in M. giganteus was genetically more distinct from the sibling species in M. robustus/M. parryi than to a related but morphologically dissimilar nematode, Ma. yamagutii from M. fuliginosus. This suggests an evolutionary parallel between host and parasite at the genetic level which is not reflected by morphological differences.

SUMMARYThis study examined whether allelic changes observed when clinical isolates ofGiardia intestinalismade in suckling mice were adapted toin vitrogrowth occurred as a result of gene switching (alternate isoenzymes) or through selection of organisms with different genotypes from mixed infections. Samples were compared electrophoretically at 20 enzyme loci. Marked allelic differences were detected between the uncloned clinical isolates grown in mice and the axenic cultures established from them. Furthermore, the allelic profiles of the uncloned isolates changed during the course ofin vivoorin vitrogrowth. In contrast, all clones produced from each isolate retained identical allelic profiles, regardless of whether they were grownin vivoorin vitro. These findings argue against gene switching as an explanation for the observed allozyme changes and support preferential selection of organisms with specific genotypes by growth conditions. The data indicate the presence of at least 2 and possibly up to 4 distinct genotypes within each clinical isolate. The genetic differences detected between clinical isolates in suckling mice were of similar magnitude to those that separate different axenic isolates ofG. intestinalisinto cryptic species. Conversely, the genetic differences between the isolates were limited when sampled after establishmentin vitro. These findings have significant implications for research onGiardiaand other medically important parasites and raise the possibility that culture may exert a similar selective bias on the genotypes isolated from infections with other parasitic protozoa.

An electrophoretic study of Pelecitus roemeri from Macropus robustus, M. giganteus and Wallubia bicolor revealed no genetic differences at 23 enzyme loci. The genetic data support the existing morphological evidence that P. roemeri from these three hosts represents a single species. The data show no genetic variation between nematodes from the same or different host species collected in northern and southern Australia. This result is discussed briefly in relation to Price's model of parasite speciation.

Allozyme electrophoresis of 98 Hypodontus macropi from eight different species of hosts using 24 enzymes revealed a complex of at least six sibling species, with 15–50% fixed genetic differences between taxa. Except for the taxon parasitizing Macropus rufus/M. robustus , pairs of parasite taxa were, in each case, sympatric at each locality examined, thus supporting the conclusion that they represent valid species. The existence of a series of host-specific nematode taxa explains many of the inconsistencies noted previously in the host distribution of H. macropi . Comparison of parasite allozyme phenograms with host phylogeny suggests that four of the speciation events could be attributable to cospeciation and two to host switching. A clear case of host switching between M. rufus/M. robustus and M. fuliginosus was found.

Evidence is presented based on morphological, electrophoretic and behavioural data, and on geographical distribution, that Aponomma tachyglossi Roberts is an independent species parasitic primarily on echidnas. Females of A. tachyglossi are distinguishable from the closely related species A. hydrosauri (Denny), parasitic on reptiles, in the shape of the porose areas, and males by the extent of the punctate areas between the scutum and the festoons. Nymphs and larvae of the two species could not be distinguished. In electrophoretic studies, A. tachyglossi was found to differ from A. hydrosauri at 16% of the 18 loci examined. Larvae of A. tachyglossi failed to attach and engorge on lizards, the usual host of A. hydrosauri. Futhermore, A. tachyglossi was found to have a limited geographical range in coastal areas of central Queensland. These data support the hypothesis that A. tachyglossi is a distinct species.

The occurrence of species flocks within the nematode genus Cloacina was examined using the criteria of host specificity, co-occurrence and monophyly. Species of Cloacina generally exhibited a high degree of host specificity, with most species occurring either in a single host species or in two closely related host species. The frequency distribution of numbers of component species of Cloacina per host species indicated that most host species harboured 2–4 species of nematodes, with an approximately exponential decline in the number of species of parasites to a maximum of 20 species of nematode per host species. Host species harbouring eight or more species of Cloacina were found within a single recent macropodid clade, but there was no correlation between evolutionary age of the host and the number of parasite species harboured. Sampling effort was significantly correlated with the number of nematode species found and, in partial regression analysis, subsumed the effects of host body size and geographic range, which were found to be significant correlates with the number of nematode species present in preliminary analyses. Analysis of co-occurrences of nematode species indicated significant variation between host species, with some hosts (e.g. Macropus agilis) most commonly harbouring a single species of Cloacina, while closely related host species (e.g. M. dorsalis) most commonly harboured numerous species. Parsimony analysis of species of Cloacina based on morphological data suggested that while small series of related nematode species could be identified within a single host species, the species flock in each host species is polyphyletic in origin. Species flocks contributed significantly to community richness in some host species.

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.