Description of Pomphorhynchus spindletruncatus n. sp. (Acanthocephala: Pomphorhynchidae) from freshwater fishes in northern Iraq,with the erection of a new pomphorhynchid genus,Pyriproboscis n. g., and keys to genera of the Pomphorhynchidae and the species of Pomphorhynchus Monticelli, 1905

The status of species of Pomphorhynchus Monticelli, 1905 is examined and 23 species are recognised as valid. These include P. spindletruncatus n. sp., which is described herein from two species of freshwater fishes in northern Iraq, Aspius vorax Heckel and Barbus xanthopterus (Heckel) (Cyprinidae). Only one other species, P. yunnanensis Wang, 1981, has a spindle-shaped trunk similar to that of P. spindletruncatus, but is distinguished from it by a distinctly different proboscis armature. A key separating the new taxon from other species of Pomphorhynchus is included. P. heronensis Pichelin, 1997 is reassigned to a new pomphorhynchid genus, Pyriproboscis n. g., based on its unique proboscis shape and armature, short proboscis receptacle and tubular cement glands. A key to the genera of the Pomphorhynchidae is also included.     

A review of the Arhythmacanthidae (Acanthocephala) with a description of Heterosentis hirsutus n. sp. from Cnidoglanis macrocephala (Plotosidae) in Australia

Heterosentis hirsutus n. sp. is described from Cnidoglanis macrocephala (Siluriformes: Plotosidae) from the Swan Estuary, Western Australia. It is distinguished by having 14 longitudinal rows of 6-7 hooks per row on the proboscis, a trunk armed anteriorly and posteriorly (= genital spines) with minute spines and lemnisci that may extend to the posterior margin of the proboscis receptacle. The new species also has prominent fragmented nuclei in its trunk wall. New information is given for Heterosentis plotosi Yamaguti, 1935 from Plotosus lineatus (Siluriformes: Plotosidae) and H. paraplagusiarum (Nickol, 1972) Amin, 1985 from Paraplagusia guttata (Pleuronectiformes: Cynoglossidae), both from Queensland. A key to the species of Heterosentis Van Cleave, 1931 is provided. The Arhythmacanthidae subfamilies are reviewed: there is little utility in the recognition of these taxa because of the small number of genera involved and the validity of the characters on which they are based is in doubt, particularly whether trunk spines are present or absent. Only Acanthocephaloides Meyer, 1932, Breizacanthus Golvan, 1969, Euzetacanthus Golvan & Houin, 1964, Heterosentis, Hypoechinorhynchus Yamaguti, 1939 and Paracanthocephaloides Golvan, 1969 of the Arhythmacanthidae are considered valid. A key to these genera is provided. The monotypic genus Neoacanthocephaloides Cable & Quick, 1954 is considered a new synonym of Acanthocephaloides thus creating Acanthocephaloides spinicaudatus (Cable & Quick, 1954) n. comb. Arhythmacanthus Yamaguti, 1935 is maintained as a synonym of Heterosentis because the distinction between two and three hook types is made equivocal when the transition between the apical and subapical hooks is gradual.     

Acanthocephalus?amini n. sp. (Acanthocephala: Echinorhynchidae) from the freshwater fish Cichlasoma?urophthalmus (Günther) (Cichlidae) in Mexico

Acanthocephalus amini n. sp. (Palaeacanthocephala: Echinorhynchidae) is described from the intestine of Cichlasoma urophthalmus (Günther) (Pisces: Cichlidae) collected in the Río Champotón, a river in Campeche State, Mexico. It is the fourth species of Acanthocephalus Koelreuther, 1771 described from North American freshwater fishes, although two other species are known from South America. The new species is distinguished from other members of Acanthocephalus by features of its trunk, which is small, clavate, slightly expanded medially and bluntly pointed posteriorly. It is further distinguished by having a cylindrical proboscis armed with 13–14 longitudinal rows of 11–12 stout hooks; the apical and medial proboscis hooks are almost uniform in size and shape, decreasing in size towards the base; the posteriormost hooks are smaller, straighter and more slender than the anterior and middle hooks; and the lateral rows of hooks are more widely spaced, forming a conspicuous longitudinal area devoid of hooks. Furthermore, the lemnisci are saccate and shorter than the proboscis receptacle; and the neck is very short with a thick collar of trunk tegument, which encircles the base of proboscis. In males, the testes are in the middle third of trunk, diagonal, spherical and small relative to the body size, and there are six clavate cement glands. In females, the uterus forms a conspicuous, elongate, cylindrical egg reservoir. The new species is most similar to A. alabamensis Amin & Williams, 1983, but can be distinguished by its swollen, clavate trunk, the largest proboscis hooks being present apically and medially, smaller testes, a shorter male reproductive system relative to body size and females with a prominent uterus. They have different hosts and geographical distribution. The new species can be differentiated from Brasacanthus sphoeroides Thatcher, 2001, a similar species in a monotypic echinorhynchid genus, because the latter is larger, has smaller proboscis hooks and its lemnisci are longer than the receptacle.     

On a new acanthocephalan family and a new order, from birds in Vietnam

During November 2000, a collection of acanthocephalans from birds in Quang Ninh Province, Vietnam, included a new genus and species in a new family and order. Pyrirhynchus heterospinus n. gen., n. sp. (Pyrirhynchidae n. fam.: Heteramorphida: new order) is described from Actitis hypoleucos (Linnaeus, 1758) (common sandpiper). The new family combines characters from Polymorphidae and Heteracanthocephalidae, and it includes new features. Specimens of the new species are distinguished from those of Heteracanthocephalidae and/or Polymorphidae by their long cylindrical trunk with anterior swelling, pyriform proboscis with hooks much larger ventrally, brain at the anterior end of the receptacle, specialized tubular cement glands, and elliptoid eggs with concentric shells. A detailed analysis of proboscis and trunk armature is included, and specimens of several species of Arhythmorhynchus Lühe, 1911 (Polymorphidae) were studied for comparative purposes. The proboscis of P. heterospinus is armed with 17 to 20 rows of 17 to 19 hooks each, with anterior 9-11 hooks rooted and posterior 6-10 spines rootless.     

First report of Neoechinorhynchus (Acanthocephala: Neoechinorhynchidae) from marine fish of the eastern seaboard of Vietnam, with the description of six new species

The occurrence of acanthocephalans of the genus Neoechinorhynchus Stiles and Hassall, 1905 in Vietnamese waters is reported for the first time. Six new species are described from seven species of marine fish of the families Belonidae, Clupeidae, Megalopidae, Mugilidae, and Sciaenidae, collected in Halong Bay of the eastern seaboard of Vietnam in 2008 and 2009. These are Neoechinorhynchus (Neoechinorhynchus) plaquensis n. sp. characterized by dermal plaques covering the entire trunk; Neoechinorhynchus manubriensis n. sp. with very long anterior proboscis hooks having roots with prominent anterior manubria and very small and equal middle and posterior hooks, two pseudo-retractors in the receptacle, simple vagina, and terminal gonopore; Neoechinorhynchus pennahia n. sp. with equal anterior and middle proboscis and somewhat smaller posterior hooks, and terminal female gonopore; Neoechinorhynchus ampullata with many giant nuclei in the body wall and lemnisci and a parareceptacle structure complex which includes pumping ampullas reported for the first time; Neoechinorhynchus (Neoechinorhynchus) longinucleatus n. sp. with very long giant nuclei in the Lemnisci, anteriorly twisted vagina, and subterminal female gonopore. Neoechinorhynchus (Neoechinorhynchus) ascus n. sp. is the second species of Neoechinorhynchus found with the parareceptacle structure/ampulla complex. Neoechinorhynchus (Neoechinorhynchus) johnii Yamaguti, 1929 of Bilqees, 1972 is not N. johnii because of proboscis armature and other discrepancies with the Yamaguti material. Notes on host distribution and feeding habits are also included.     

Description and morphological variability of <Emphasis Type="Italic">Neoechinorhynchus beringianus</Emphasis> n. sp. (Acanthocephala: Neoechinorhynchidae) from north-eastern Asia

Neoechinorhynchus beringianus sp. n. is described from Pungitius pungitius L. in north-eastern Russia. Since 1986, when it was first found, it was reported as 'N. pungitius Dechtiar, 1971'. However, this new species differs from the latter in having an egg shell without a prolongation of the fertilisation membrane, a larger proboscis and proboscis hooks, a subterminal position of the female genital pore and a more slender trunk, and it occurs in a different site in the intestine. N. beringianus has a small, stout body with an asymmetrical position of the proboscis, which is located ventrally to and at an angle with the longitudinal axis of the body. The proboscis is wider than long, the hooks are of equal size in each circle but diminish in size posteriorly, whereas the lemnisci are subequal in length. It differs from those species of Neoechinorhynchus Stiles & Hassall, 1905 with somewhat similar characteristics in body length, proboscis size and proportions, proboscis hook lengths, egg size, size-ratio of the cement gland and testes, and the number of giant nuclei in the tegument and lemnisci. In different geographical populations of the new species, the sizes of both the proboscis and proboscis hooks exhibit some variation.     

Neoechinorhynchus (Neoechinorhynchus) dorsovaginatus n. sp.(Acanthocephala: Neoechinorhynchidae) from the dusky kob Argyrosomus japonicus (Sciaenidae) on the southern coast of South Africa

Neoechinorhynchus (Neoechinorhynchus) dorsovaginatus n. sp. (Acanthocephala: Neoechinorhynchidae) is described from the dusky kob, Argyrosomus japonicus (Temminck & Schlegel) from the southern coast of South Africa in the Breede River Estuary. Like four other species of Neoechinorhynchus Stiles & Hassall, 1905, N. (N.) africanus Troncy, 1969, N. (N.) johnii Yamaguti, 1939, N. topseyi Podder, 1937 and N. (N.) tylosuri Yamaguti, 1939, the new species has a very long, slender body, cylindrical testes and cement-gland, anterior proboscis hooks much longer than the middle or posterior hooks, and a long neck. The new species is the only species of Neoechinorynchus having an antero-dorsal hump just posterior to the neck and a specialised vaginal sphincter and a gonopore on the dorsal side. It is closest to N. (N.) johnii, but is distinguished from it by: the size of the trunk, proboscis, anterior proboscis hooks, neck, and the posterior testis in relation to the cement-gland; the shape of cerebral ganglion and proboscis hook root; and the number of giant nuclei in the cement-gland.     

Description and pathology of Neoechinorhynchus idahoensis n. sp. (Acanthocephala: Neoechinorhynchidae) in Catostomus columbianus from Idaho.

Neoechinorhynchus idahoensis is described from Catostomus columbianus caught in the Salmon River, Stanley Basin, Idaho. The new species is closest to Neoechinorhynchus venustus Lynch, 1936, but is distinguished from it by its smaller and variably structured eggs, anterio-dorsal trunk hump, bent and posteriorly notched proboscis receptacle, and larger proboscis, proboscis receptacle, and hooks. It is distinguished also from 2 other species of Neoechinorhynchus with proboscis hooks in middle and anterior circles about equally large and from 7 other species having lemnisci greatly unequal in length. Histopathology of host tissue showed limited host response exemplified by epithelial damage and hemorrhaging at point of proboscis attachment with subsequent macrophage and other phagocytic cell migration. The proboscis extended through the host epithelium into the submucosa with limited hemorrhaging at the point of attachment. Unorganized collagenous fibers were present. The lumen of the host intestine was obstructed, and compressed villi were present. The trunk of the worm damaged intestinal epithelium near the crypts, causing localized inflammation. The caryophyllaeid cestode Isoglaridacris calentinei Mackiewicz, 1974, was present in concurrent infections of C. columbianus.     

Description and host relationships of Polymorphus spindlatus n. sp. (Acanthocephala: Polymorphidae) from the heron Nycticorax nycticorax in Peru

Polymorphus spindlatus n. sp. is described from the black-crowned night heron, Nycticorax nycticorax, in Lake Titicaca, Peru. It is distinguished from all 27 known species of the subgenus Polymorphus by its spindle-shaped proboscis and its trunk shape, the anterior 2/3 of which is ovoid, tapering into a tubular posterior end. It resembles Polymorphus brevis (=Arhythmorhynchus brevis), which is, however, longer and considerably more slender, and has smaller and more numerous proboscis hooks per row and smaller eggs. It is separated also from Polymorphus swartzi, Polymorphus striatus, Polymorphus contortus, and Polymorphus cincli by its proboscis armature (usually 18 longitudinal rows of 11-13 hooks each), among other characters. Histopathological sections of host tissue show well defined localized damage including hemorrhaging with subsequent phagocyte cell migration (granular tissue). The lumen of the host intestine is obstructed and villi show compression. The proboscis of P. spindlatus extends through the intestinal mucosa and submucosa, displacing the smooth muscle layers of the muscularis externa. Fibrosis also was observed.     

Plagiorhynchidae Meyer, 1931 (Acanthocephala) from Australasian birds and mammals,with descriptions of Plagiorhynchus (Plagiorhynchus) menurae (Johnston, 1912) and P. (P.) allisonae n. sp.

New host and locality records are given for Plagiorhynchus (Plagiorhynchus) charadrii (Yamaguti, 1939) Van Cleave, 1951 and P. (Prosthorhynchus) cylindraceus (Goeze, 1782) Schmidt & Kuntz, 1966. The uncertainty of identification of a plover host of P. (P.) charadrii as well as the origins of P. (P.) cylindraceus (found in Australia but not New Zealand) and its occurrence in both bird and mammal hosts are discussed. P. (P.) menurae (Johnston, 1912) Golvan, 1956 is redescribed, including the male, and new host, Menura alberti Bonaparte, and locality records are given. P. (P.) allisonae n. sp. is described from Haematopus ostralegus finschi (Martens) and H. unicolor (Forster) from the South Island of New Zealand. P. (P.) allisonae can be differentiated from its congeners by having a proboscis armature of 18-23 rows of 14-20 hooks, thorns of hooks shorter than simple roots with short manubria, eight tubular cement glands and eggs of 134-154 x 33-36 microm in size. The presence of P. (P.) gracilis Petrochenko, 1958 in Australia is questioned. New host and locality records are given for Porrorchis hylae (Johnston, 1914) Schmidt & Kuntz, 1967 and the northern distribution of P. hydromuris (Edmonds, 1957) Schmidt & Kuntz, 1967 confirmed.     

Pomphorhynchus patagonicus n. sp. (Acanthocephala: Pomphorhynchidae) from freshwater fishes of Patagonia, Argentina

Pomphorhynchus patagonicus n. sp. is described from Lake Rosario, Chubut Province, Argentina. It is characterized by a long neck forming an asymmetrical bulb with 2 well differentiated dorsal protruberances and 14 alternating rows of 13 and 14 proboscis hooks, each row with a stout fourth hook. It most closely resembles Pomphorhynchus sebastichthydis Yamaguti, 1939, from Japan, but differs in the bulb protruberances and in having more rows of hooks and more hooks per row and in the shapes of the fourth and basal hooks. Among American species P. patagonicus shows some similarities to Pomphorhynchus yamagutii Schmidt and Hugghins, 1973, from Chile, but differs with respect to the longer neck, bulb protruberances, and proboscis armature. Pomphorhynchus patagonicus is endemic to Patagonia, where its definitive type host is the endemic fish Patagonina hatcheri (Atherinidae) and its intermediate host the endemic freshwater amphipod Hyalella patagonica. It has been found also in autochthonous fishes belonging to the families Galaxiidae and Percichthyidae and in introduced salmonid fishes.     

The effect of host species on growth and variability of Echinorhynchus salmonis Müller, 1784 (Acanthocephala: Echinorhynchidae), with special reference to the status of the genus

Summary The sex and age (as measured by length) of Echinorhynchus salmonis Müller, 1784 and the host species of this acanthocephalan considerably affected worm body form and size, as well as size of proboscis, proboscis hooks, proboscis receptacle, lemnisci, testes and cement glands. Linear regression analysis indicated that curves describing the growth pattern of these characters by worm length were significantly different as a function of host species. The larger worms recovered from bloater (Coregonus hoyi: Salmonidae) almost invariably showed higher regression coefficient compared to those from smelt (Osmerus mordax: Osmeridae) in all characters. Taxonomic implications of these findings are discussed. Abnormalities in body wall, proboscis hook orientation, lemnisci and cement gland ducts as well as variations in proboscis hook and cement gland numbers are reported, some for the first time. Findings from studies of cement gland pattern invalidate Petrochenko's (1956) splitting up of the genus into three: Echinorhynchus, Metechinorhynchus and Pseudoechinorhynchus. It is proposed that the designation of the last two genera as junior synynoms of the first be accepted. ac]19791205     

Status of Corynosoma (Acanthocephala: Polymorphidae) based on anatomical, ecological, and phylogenetic evidence, with the erection of Pseudocorynosoma n. gen

The possession of genital spines has been considered as a key taxonomic trait to differentiate Corynosoma from other genera of the Polymorphidae. However, Corynosoma currently consists of 2 groups of species with clear ecological and morphological divergences: the "marine" group (with ca. 30 species) infects mammals and piscivorous birds in the marine realm, whereas the "freshwater" group (with ca. 7 species) infects waterfowl in continental waters. Species from these groups differ in shape of body and neck, trunk spination, lemnisci length and shape, testes arrangement, and number and shape of cement glands. We tested whether species from these 2 groups formed a monophyletic assemblage based on a phylogenetic analysis by using 15 morphological characters. We also included species of Andracantha, Polymorphus, and Hexaglandula with which potential taxonomic conflicts could most likely arise. We obtained 108 equally most parsimonious trees of 32 steps, with a consistency index (CI) = 0.59, and a retention index (RI) = 0.82. The strict consensus tree indicated that the "freshwater" species of Corynosoma form a monophyletic assemblage closely related to some species of Polymorphus, whereas the "marine" species of Corynosoma are grouped together with Andracantha. Accordingly, Corynosoma is not a monophyletic assemblage, and Pseudocorynosoma n. gen. is proposed for the "freshwater" species of Corynosoma. This decision was strongly supported by (1) a functional comparison of foretrunk muscles between species of Polymophus, Andracantha, and Corynosoma; (2) a multivariate morphometric study of proboscis characters and egg size; and (3) an analysis of ecological patterns of host-parasite relationships.     

<Emphasis Type="Italic">Acanthocephaloides irregularis</Emphasis> n. sp. (Acanthocephala: Arhythmacanthidae) from marine fishes off the Ukrainian Black Sea coast

Acanthocephaloides irregularis n. sp. (Arhythmacanthidae) is described from four species of marine fishes in the Gulf of Odessa and Sukhyi Lyman, Ukrainan Black Sea waters, making it the tenth species of the genus. The hosts are the combtooth blenny Parablennius zvonimiri (Kolombatovic) (Blenniidae), the mushroom goby Ponticola eurycephalus (Kessler) (Gobiidae), the tubenose goby Proterorhinus marmoratus (Pallas) (Gobiidae) and the black-striped pipefish Syngnathus abaster Risso (Syngnathidae). The new species is most similar to its closest relative, Acanthocephaloides propinquus (Dujardin, 1845), in proboscis shape and armature (12 longitudinal rows of 5 hooks) and the shape of the trunk, reproductive system and lemnisci, but differs in having randomly distributed trunk spines. These trunk spines are organised in circular rings of individual spines separated by aspinose zones. The new species is also unique in having an anterior trunk collar, a very large triangular cephalic ganglion, nucleated pouches at the posterior end of the proboscis receptacle, and hooks and spines with roots bearing anterior manubria. Valid and invalid species of Acanthocephaloides Meyer, 1932 are listed and a key to all ten species is included.     

A revision of Microbothriorhynchus Yamaguti, 1952 (Cestoda: Trypanorhyncha), with the redescription of M coelorhynchi Yamaguti, 1952 and the description of M reimeri n sp

The genus Microbothriorhynchus Yamaguti, 1952 is revised. Plerocerci of M. coelorhynchi Yamaguti, 1952 from the body-cavity of Brotula barbata (Bloch & Schneider) off the Angolan coast are re-described, and M. reimeri n. sp. from the body-cavity of Helicolenus maculatus (Cuvier) and Caelorinchus parallelus (Günther) from coastal waters off Mozambique is added to the genus. Both species are characterised in having an elongated, slightly craspedote scolex with small, collar-like bothridia, an elongate pars vaginalis and very long bulbs. The tentacular armature is heteroacanthous atypica, with eight principal hooks and intercalary hooks merging with a band of spiniform hooks on the external tentacle surface. The adult is unknown. Microbothriorhynchus is allocated to the Lacistorhynchidae Guiart, 1927, in having a blastocyst, two bothridia and a heteroacanthous atypica armature. Dasyrhynchus Pintner, 1928 and Pseudogrillotia Dollfus, 1969 are considered the most closely related genera, sharing characters such as the craspedote scolex, similar scolex proportions and hook patterns. Microbothriorhynchus appears to link the heteroacanthous atypica genera Grillotia Guiart, 1927 and Pseudogrillotia with the poeciloacanthous genus Dasyrhynchus.     

<Emphasis Type="Italic">Mayarhynchus karlae</Emphasis> n. g., n. sp. (Acanthocephala: Neoechinorhynchidae), a parasite of cichlids (Perciformes: Cichlidae) in southeastern Mexico,with comments on the paraphyly of <Emphasis Type="Italic">Neoechynorhynchus</Emphasis> Stiles &amp; Hassall, 1905

Mayarhynchus n. g. (Acanthocephala: Neoechinorhynchidae) is erected for Mayarhynchus karlae n. g, n. sp. described from the intestine of four species of cichlid fishes distributed from southeastern Mexico. The new genus placed in the family Neoechinorhynchidae (Ward, 1917) Van Cleave, 1928, is readily distinguished from the other 17 genera in the family by having a small proboscis armed with 45–46 relatively weak rooted hooks arranged in nine longitudinal rows of five hooks each. In addition, Mayarhynchus n. g., n. sp. is diagnosed by the presence of a short trunk, body wall with five dorsal and one ventral giant hypodermal nuclei, proboscis receptacle nearly cylindrical with single layered wall, lemnisci broad and flat with large nuclei, testes in tandem, cement gland with eight large nuclei, and eggs elongate to oval. Partial sequences of the cytochrome c oxidase subunit 1 (cox1), internal transcribed spacers (ITS1 + 5.8S + ITS2), and the D2-D3 domains of the large subunit rRNA gene (28S) were obtained for five specimens of the new species and other species belonging to the Neoechinorhynchidae. Phylogenetic analyses confirmed that the new genus belongs to the Neoechynorhynchidae and indicated that the genus Neoechynorhynchus Stiles & Hassall, 1905 is not monophyletic. Comparison between three populations of the new species yielded nine variable sites for cox1, 11 for ITS and four for 28S.     

Amapacanthus amazonicus n. g., n. sp. (Acanthocephala: Diplosentidae: Allorhadinorhynchinae) from Arius passany and Anableps microleps (Pisces) at Maraca Island off northern Brazil

Amapacanthus amazonicus n. g., n. sp. is described from the intestine of Arius passany (Valenciennes) and Anableps microleps Müller. The most important diagnostic features are: a small globular proboscis armed with 6 diagonal rows of 3 stout hooks; middle hooks conspicuously stouter and larger than anterior ones; terminal hooks as long as middle hooks but straighter and more slender; a double-walled proboscis receptacle; a trunk bearing spines anteriorly; and two tubular cement glands in the males. Amapacanthus n. g. is differentiated from Allorhadinorhynchus, Golvanorhynchus and Slendrorhynchus, the other genera of the Allorhadinorhynchinae, by the presence of a globular proboscis armed with a small number (18) of hooks. A key to the species of the Allorhadinorhynchinae is presented.     

Validating the systematic position of Profilicollis Meyer, 1931 and Hexaglandula Petrochenko, 1950 (Acanthocephala: Polymorphidae) using cytochrome c oxidase (Cox 1)

Members of the Polymorphidae (Acanthocephala) are distributed worldwide as endoparasites of marine mammals, fish-eating birds, and waterfowl. The family contains 10 genera, with approximately 127 species. Polymorphids are characterized by having a spinose trunk with a bulbous proboscis, double-walled proboscis receptacle, long lemnisci, and 4 tubular cement glands. The taxonomic position of several genera within Polymorphidae has been controversial when considering morphological and ecological characters. The mitochondrial coding gene cytochrome-c oxidase representing species of 5 genera of polymorphids (Corynosoma, Lühe, 1904, Hexaglandula Petrochenko, 1950, Southwellina Witenberg 1932, Polymorphus Luh?, 1911, and Profilicollis Meyer, 1931) were sequenced to determine the sister-group relationships among 2 particular genera, i.e., Hexaglandula, and Profilicollis. Maximum likelihood and Bayesian analyses showed that Polymorphidae is a monophyletic assemblage, and that 3 major clades are present. Our results provide support for the idea that Hexaglandula represents an independent lineage, whereas, in the case of Profilicollis, there is no conclusive evidence that they are not members of Polymorphus. The analyses also confirm that Polymorphus is paraphyletic, suggesting that the genus represents a complex of species that should be reexamined and reclassified using morphological, ecological, and molecular data. Our observations suggest that decapods (intermediate hosts for the 2 genera under study) were independently colonized at least twice during the evolutionary history of the group.     

New morphological data on the acanthocephalan <Emphasis Type="Italic">Hypoechinorhynchus magellanicus</Emphasis> Szidat, 1950 (Palaeacanthocephala: Arhythmacanthidae)

Hypoechinorhynchus magellanicus Szidat, 1950 (Acanthocephala: Arhythmacanthidae) is redescribed based on specimens collected from a sub-Antarctic notothenioid fish, Champsocephalus esox (Günther). The host was caught in the Beagle Channel (Magellanic sub-region). H. magellanicus has a trunk with an antero-dorsal curvature, a spherical proboscis, spines on the anterior region of the trunk, narrow lemnisci which are considerably longer than the proboscis receptacle, six cement glands and a single vaginal sphincter. The proboscis is armed with 40 hooks, including 15 large hooks with roots and 25 rootless basal spines. The large hooks are arranged in 10 alternate rows of one and two hooks. Each single large hook is followed by two spines, and pairs of large hooks are followed by single spines. Ten single spines are also present at the base of the proboscis between the rows. The eggs have polar prolongations of the middle envelope.     

Species of Mediorhynchus (Acanthocephala: Gigantorhynchidae) in Australian birds with the description of Mediorhynchus colluricinclae n. sp.

Four species of Mediorhynchus are identified from Australian birds. New locality records are given for Mediorhynchus alecturae (Johnston and Mawson, 1947) Golvan, 1962 and new host and locality records for M. corcoracis Johnston and Edmonds, 1951. Mediorhychus grandis has been reported from Australian hosts, but this record could not be verified. Two females from Acanthogenys rufogularis and the anterior portion of a single female from a "gull" had characters of proboscis armature, lemnisci, and eggs that precluded them being assigned to any of the presently known species of Mediorhynchus. Mediorhynchus colluricinclae n. sp. was found in pomatostomatids from South Australian localities. A high degree of host specificity is recorded for M. corcoracis and M. colluricinclae. Selection of specific dietary items may be one filter that influences the degree of host specificity encountered.