Helminths from the giant mottled eel Anguilla marmorata Quoy & Gaimard in Japan,with a description of Acanthocephalus longiacanthus n. sp. (Acanthocephala: Echinorhynchidae)

Five helminths, including a new echinorhynchid acanthocephalan Acanthocephalus longiacanthus n. sp., are described based on specimens from the giant mottled eel Anguilla marmorata Quoy & Gaimard caught in a small river, western Japan. The new acanthocephalan is distinguished from the other congeners in terms of hook arrangement (8–9 longitudinal rows with 5–6 hooks per row) on proboscis, maximum length of hook blade (81–95 μm in male, 150–190 μm in female), lemnisci being longer than proboscis receptacle, and small-sized eggs (80–83 μm). Two monogeneans, Pseudodactylogyrus anguillae (Yin & Sproston, 1948) and P. bini (Kikuchi, 1929), and two acanthocephalans, Acanthocephalus gotoi Van Cleave, 1925 and Southwellina hispida (Van Cleave, 1925), were also found; this new material is described. The monogeneans are notorious as invasive parasites spreading worldwide via anthropogenic transportations of anguillid eels, but in Japanese waters A. marmorata appears to be an indigenous host for these parasites. Anguilla marmorata is a new host record for the acanthocephalans A. gotoi and S. hispida.     

Acanthocephalus tahlequahensis sp. n. (Acanthocephala: Echinorhynchidae) from the the stippled darter, Etheostoma punctulatum (Agassiz), in northeastern Oklahoma.

Acanthocephalus tahlequahensis sp. n. was recovered from the intestines of 4 species of freshwater fishes, Etheostoma punctulatum, E. spectabile, Nocomis asper, and Notropis pilsbryi, collected in northeastern Oklahoma. The new species is distinguished from all other species of Acanthocephalus, except A. japonicus (Fukui and Morisita 1936) Petrochenko 1956, and A. fluviatilus Paperna 1964, by having smaller proboscis hooks. The length of the proboscis hooks for males is 27 to 38 (33) mum and for females 35 to 46 (42) mum. A. tahlequahensis is smaller than either A. japonicus or A. fluviatilis, and has about half the number of longitudinal rows of proboscis hooks of A. japonicus and half the number of proboscis hooks in each longitudinal row of A. fluviatilus. In addition to having smaller hooks. A. tahlequahensis differs from other species of Acanthocephalus parasitizing North American fishes by its smaller, spindle-shaped trunk and more hooks in each longitudinal row.     

<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.     

First morphological and molecular characterization of cystacanths of Corynosoma evae Zdzitowiecki, 1984 (Acanthocephala: Polymorphidae) from Antarctic teleost fishes

Cystacanths of the polymorphid acanthocephalan Corynosoma evae Zdzitowiecki, 1984 were examined and redescribed based on newly collected material from teleost fishes from coastal waters of the Galindez Island (Argentine Islands, West Antarctica). Detailed morphological data, measurements and photomicrographs, including scanning electron microscopy images, are presented. Our morphological and morphometrical analyses confirmed the validity of C. evae; however, three key characteristics of taxonomic importance (i.e., the number of rows of hooks on the proboscis, and the number and arrangement of genital spines in males) showed significant morphological variability. In addition, a genital spine in the posterior body end of a female is reported for the first time. This study provides the first sequences of the small and large subunits nuclear ribosomal RNA genes (SSU and LSU) and the mitochondrial cytochrome c oxidase subunit 1 (cox1) for C. evae. Maximum likelihood and Bayesian inference analyses of the SSU + LSU + cox1 and the cox1 datasets placed C. evae as a sister lineage to a clade formed by C. validum Van Cleave, 1953 and C. villosum Van Cleave, 1953, although with low support. In contrast, the position of C. evae in the phylogenetic analysis of the SSU + LSU dataset remained unresolved. Finally, C. arctocephali Zdzitowiecki, 1984 from pinnipeds from the subantarctic and Antarctic regions is considered as a valid species.     

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.

     

A new species of Heterosentis Van Cleave, 1931 (Acanthocephala, Arhythmacanthidae), a parasite of pinguipedid fishes in the southwest Atlantic

A new species of arhythmacanthid acanthocephalan, Heterosentis martini n. sp., parasitic in the Argentinean sandperch Pseudopercis semifasciata (Cuvier) (Perciformes, Pinguipedidae) from the coasts of Argentina is described. Heterosentis martini n. sp. differs from all congeneric species by having 10 longitudinal rows of hooks in the proboscis, each with 7-8 hooks, consisting of 1 medium apical and 3 larger sub-apical hooks with root, and 3-4 smaller, basal, curved hooks with rudimentary roots and spines in both ventral and dorsal regions of the body. The most similar species, Heterosentis heteracanthus (Linstow, 1896) Van Cleave, 1931, and Heterosentis brasiliensis Vieira, Felizardo and Luque, 2009, also have 10 longitudinal rows of hooks, but H. heteracanthus differs from the new species by having only 3-5 (more frequently 4) hooks in each row, with only the anterior hook large and bearing a developed root. Heterosentis brasiliensis differs from the new species by possessing 2 sub-apical hooks in each row (instead of 3), similar body length but shorter proboscis, and trunk spines restricted to the ventral surface of body.     

Description of a new species of Moniliformis (Acanthocephala: Moniliformidae) from Peromyscus hylocetes (Rodentia: Cricetidae) in Mexico

Moniliformis ibunami n. sp., is described from the intestine of the transvolcanic deermouse Peromyscus hylocetes Merriam 1898 (Cricetidae) from Parque Nacional Nevado de Colima “El Floripondio”, Jalisco, Mexico. The new species can be distinguished morphologically from the other 18 congeneric species of Moniliformis by a combination of morphological and molecular characters including the number of hooks on the proboscis (12 longitudinal rows, each one with six to eight transversally arranged unrooted hooks), the proboscis length (230–270 μm), the female trunk length (159–186 mm) and egg size (40–70 × 20–40). For molecular distinction, nearly complete sequences of the small subunit (SSU) and large subunit (LSU) of the nuclear ribosomal DNA and cytochrome oxidase subunit 1 (cox 1) of the mitochondrial DNA of the new species were obtained and compared with available sequences downloaded from GenBank. Phylogenetic analyses inferred with the three molecular markers consistently showed that Moniliformis ibunami n. sp. is sister to other congeneric species of Moniliformis. The genetic distance with cox 1 gene among Moniliformis ibunami n. sp., M. saudi, M. cryptosaudi, M. kalahariensis, M. necromysi and M. moniliformis ranged from 20 to 27%. Morphological evidence and high genetic distance, plus the phylogenetic analyses, indicate that acanthocephalans collected from the intestines of transvolcanic deer mice represent a new species which constitutes the seventh species of the genus Moniliformis in the Americas.     

A comparative survey of proboscis morphology and associated structures in fruit-piercing, tear-feeding, and blood-feeding moths in Calpinae (Lepidoptera: Erebidae)

Functional feeding categories for adult species of Calpinae are described. Structures associated with the proboscis were examined using exemplar species in fruit-piercing, blood-feeding, and tear-feeding species using both light microscopy and SEM methods. At least three genera currently placed in Calpini, and several others in related groups lack specialized piercing structures. The proboscis of the tear-feeding species, Hemiceratoides hieroglyphica, is equipped with specialized cuticular hooks not yet observed in other tear-feeding species. Tearing hooks moveable by blood pressure are restricted to Calpini species, and little additional variation within this taxon exists, suggesting proboscis morphology may not be strongly correlated with feeding behavior (e.g., fruit piercing vs. blood feeding). A glossary of terms and character codings for proboscis structures is provided, and morphologies for all included calpine taxa are described. We discuss the taxonomic significance of proboscis morphology in Calpinae and the evolutionary implications of their associated feeding behaviors. This survey indicates morphology provides powerful prediction, but not proof of lepidopteran adult food habits.     

Acanthocephaloides cyrusi n. sp. (Acanthocephala: Arhythmacanthidae) from southeast African teleost fishes

A new species,Acanthocephaloides cyrusi, is described from the fishesSolea bleekeri andPomadasys commersoni from Lake St. Lucia, Natal, South Africa. It is distinguished from the other species in the genus by the more marked sexual dimorphism in length, the arrangement of hooks, the proboscis with the longest hooks at the anterior-most extremity and the greater size of the proboscis hooks and body spines. An acanthella, which may represent this species, was found in the tanaidApseudes digitalis.     

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.     

Morphological and molecular data for a new species of <Emphasis Type="Italic">Pomphorhynchus</Emphasis> Monticelli, 1905 (Acanthocephala: Pomphorhynchidae) in the Mexican redhorse <Emphasis Type="Italic">Moxostoma austrinum</Emphasis> Bean (Cypriniformes: Catostomidae) in central Mexico

Pomphorhynchus purhepechus n. sp. is described from the intestine of the Mexican redhorse Moxostoma austrinum Bean (Catostomidae) in central Mexico. The new species can be distinguished from the other seven described species of Pomphorhynchus Monticelli, 1905 in the Americas by a subspherical proboscis and 14 longitudinal rows with 16–18 hooks each; the third and the fourth row of hooks are alternately longest. Sequences of the mitochondrial cytochrome c oxidase subunit 1 (cox1) gene and the large subunit (LSU) rDNA (including the domains D2-D3) were used to corroborate the morphological distinction between the new species and Pomphorhynchus bulbocolli Linkins in Van Cleave, 1919, a species widely distributed in several freshwater fish species across Canada, USA, and Mexico. The genetic divergence estimated between the new species and the isolates of P. bulbocolli ranged between 13 and 14% for cox1, and between 0.6 and 0.8% for LSU. Maximum likelihood and Bayesian inference analyses of each dataset showed that the isolates of P. bulbocolli parasitising freshwater fishes from three families, the Catostomidae, Cyprinidae and Centrarchidae, represent a separate lineage, and that the acanthocephalans collected from two localities in central Mexico comprise an independent lineage. In addition, our analysis of the genetic variation of P. bulbocolli demonstrates that individuals of this acanthocephalan from different host species are conspecific. Finally, the distribution, host-association, and phylogenetic relationship of the new species, when placed in the context of the region’s geological history, suggest that both host and parasite underwent speciation after their ancestors became isolated in Central Mexico.     

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.     

Morphological and molecular data reveal a new species of Neoechinorhynchus (Acanthocephala: Neoechinorhynchidae) from Dormitator maculatus in the Gulf of Mexico

Neoechinorhynchus (Neoechinorhynchus) mexicoensis sp. n. is described from the intestine of Dormitator maculatus (Bloch 1792) collected in 5 coastal localities from the Gulf of Mexico. The new species is mainly distinguished from the other 33 described species of Neoechinorhynchus from the Americas associated with freshwater, marine and brackish fishes by having smaller middle and posterior hooks and possessing a small proboscis with three rows of six hooks each, apical hooks longer than other hooks and extending to the same level as the posterior hooks, 1 giant nucleus in the ventral body wall and females with eggs longer than other congeneric species. Sequences of the internal transcribed spacer (ITS) and the large subunit (LSU) of ribosomal DNA including the domain D2 + D3 were used independently to corroborate the morphological distinction among the new species and other congeneric species associated with freshwater and brackish water fish from Mexico. The genetic divergence estimated among congeneric species ranged from 7.34 to 44% for ITS and from 1.65 to 32.9% for LSU. Maximum likelihood and Bayesian inference analyses with each dataset showed that the 25 specimens analyzed from 5 localities of the coast of the Gulf of Mexico parasitizing D. maculatus represent an independent clade with strong bootstrap support and posterior probabilities. The morphological evidence, plus the monophyly in the phylogenetic analyses, indicates that the acanthocephalans collected from intestine of D. maculatus from the Gulf of Mexico represent a new species, herein named N. (N.) mexicoensis sp. n.     

Spiracanthus bovichthys n. gen. n. sp. (Acanthocephala: Arhythmacanthidae), a parasite of littoral fishes of the central south coast of Chile

A new acanthocephalan species, Spiracanthus bovichthys n. gen. n. sp., is described. Samples were taken from 26 marine fish species between 23 and 53 degrees S of Chile. The parasite was found in the intestine of 6 species and only between 36 and 40 degrees S, especially in those fish that prey on small crustaceans in the upper and sublittoral zone. The parasite was found in Bovichthys chilensis (Reagan). Auchenionchus variolosus (Valenciennes), Calliclinus genigutattus (Valenciennes), Sindoscopus australis (Fowler and Bean), Myxodes cristatus Valenciennes, and Gobiesox marmoratus (Jenyns). However, only the first species is a suitable host for the parasite as evidenced by the presence of mature females. This acanthocephalan belongs to Arhythmacanthidae, but it does not correspond to any genus described. Spiracanthus bovichthys is different in the number and spiralled distribution of its hooks in the proboscis. In the short proboscis, 3 groups of hooks are distinguished according to size, summing up to 150-190 hooks. The group of largest hooks are found in the apical part of the proboscis, and there are 10 diagonal rows of small hooks from the prebasal to basal proboscis. Its trunk is covered partially by small spines. Amphipod and isopods were the prey items shared among the host fish species and are the best candidates to be the intermediate hosts of S. bovichthys.     

Neoechinorhynchus (Neoechinorhynchus) chimalapasensis n. sp. (Acanthocephala: Neoechinorhynchidae) from the freshwater fish Awaous banana (Valenciennes) (Gobiidae) in Mexico

Neoechinorhynchus (Neoechinorhynchus) chimalapasensis n. sp. (Eoacanthocephala: Neoechinorhynchidae) is described from the intestine of Awaous banana (Valenciennes) (Pisces: Gobiidae) collected in the Río Negro, a tributary in the upper Río Coatzacoalcos basin, Santa María Chimalapa, Oaxaca State, Mexico. It is the third species of Neoechinorhynchus Stiles & Hassall, 1905 described from Mexican freshwater fishes, although 36 other species are known from freshwater fishes in the Americas. Like four other species of Neoechinorhynchus from freshwater fishes in North America and Mexico, N. (N.) limi Muzzall & Buckner, 1982, (N.) rutili (Müller, 1780) Stiles & Hassall, 1905, N. (N.) salmonis Ching, 1984 and N. (N.) roseus Salgado-Maldonado, 1978, males and females of the new species are less than 20 mm in length, lack conspicuous sexual dimorphism in size, have a small proboscis of about 0.1 mm in length with the largest hooks being the anteriormost, about 30–90 μm in length and of equal size, and have subequal lemnisci, larger than the proboscis receptacle but still relatively short and, in males, generally restricted to a position considerably anterior to the testes. The new species is closest to N. (N.) roseus, but it is distinguished from it by having: (1) a slightly larger cylindrical proboscis with almost parallel sides versus a globular proboscis with a rounded tip which is shorter and somewhat wider in N. (N.) roseus; (2) smaller but robust anterior proboscis hooks that do not reach the equatorial level or extend beyond the hooks of the middle circle as in N. (N.) roseus; and (3) the female gonopore situated ventrally subterminal, as opposed to being a significant distance anteriorly to the posterior extremity in N. (N.) roseus.     

Cystacanths of Acanthocephala in notothenioid fish from the Beagle Channel (sub-Antarctica)

The morphology of relaxed cystacanths of polymorphid acanthocephalans collected from notothenioid fishes in the Beagle Channel (Magellanic subregion of sub-Antarctica) is described. A parasite of birds, Andracantha baylisi (Zdzitowiecki, 1986), was found in Patagonotothen longipes and Champsocephalus esox. It has: a proboscis 0.82–0.89 mm long; a proboscis hook formula of 16 rows of 9/10–10/11, including 4–5 basal hooks; distal hooks with the longest blades; a fore-trunk not separated from the hind-trunk by a constriction; large somatic spines arranged in two zones separated by a zone of small, loosely dispersed spines; and only the anterior 36–40% of ventral side of the trunk is covered with spines. One male specimen of Corynosoma sp. was found in Patagonotothen tessellata. It differs from A. baylisi in that the distal proboscis hooks are similar in length to the prebasal hooks, it has a smaller proboscis (0.77 mm) and in the distribution of the somatic spines, which are contiguous with the genital spines on the ventral side of the trunk and lack a zone of small spines between zones of larger spines. A parasite of seals and fur seals, Corynosoma evae Zdzitowiecki, 1984, was found in P. longipes and Champsocephalus esox. It has: a proboscis 0.61–0.78 mm long; a proboscis hook formula of 20–22 rows of 12–13, including 3/4–4 basal hooks; prebasal hooks with the longest blades; a trunk divided into fore-trunk and hind-trunk; somatic spines covering the anterior 64–74% of the ventral side of the trunk; genital spines present only in males; and a terminal genital opening in both sexes. Corynosoma beaglense n. sp. was found in Champsocephalus esox. It has: an almost cylindrical proboscis (length 0.52–0.56 mm); a proboscis hook formula of 16 rows of 9/10–10/11, including 4–4/5 basal hooks; distal hooks shorter than the prebasal hooks; a fore-trunk not separated from the hind-trunk by a constriction; somatic spines contiguous with the genital spines on the ventral side of the trunk of the male and covering the entire length of the ventral side of the female trunk, and the presence of genital spines surrounding the terminal genital pore of the male. The definitive host of this species is unknown.     

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.