Three new species of Polyclithrum Rogers, 1967 (Gyrodactylidae: Monogenea) from mugilid fishes from Australia and Brazil, with a redescription of P. mugilini Rogers, 1967

Polyclithrum mugilini Rogers, 1967, a parasite of Mugil cephalus Linnaeus, is redescribed from type-material from Lake Seminole, Georgia, USA. Three new species of Polyclithrum Rogers, 1967 are also described: P. alberti n. sp. from M. cephalus from the Albert River, Queensland, Australia; P. boegeri n. sp. from M. platanus Günther from Rio da Guarda, State of Rio de Janeiro, Brazil; and P. corallense n. sp. from M. cephalus from Heron Island, Great Barrier Reef, Australia. The four species can be distinguished by the size and shape of haptoral sclerites, but in particular by accessory bar number 3, the dorsal bar, the marginal hooks and the hamulus point to shaft angle. The validity of Micropolyclithrum parvum Skinner, 1975, a parasite of M. cephalus in Biscayne Bay, Florida, is discussed, and a key to the species of Polyclithrum is presented.     

The description of Gyrodactylus mulli sp. n. (Monogenea: Gyrodactylidae) from the Black Sea blunt-snouted mullet Mullus barbatus ponticus

A new species Gyrodactylus mulli sp. n. is described from the thorax fins of blunt-snouted mullet Mullus barbatus ponticus by the collections of B. E. Bychowsky made in 1947 near Karadag on the Black Sea. Gyrodactylus mulli sp. n. differs from G. alviga Dmitrieva et Gerasev, 2000 (described from blunt-snouted mullet too) in having another morphotype of the marginal hooks. The new species differs from G. proterorhini Ergens, 1967, which has the identical type of the marginal hooks, in having longer membrane of the ventral connective bar, longer point of the anchors, shorter marginal hooks, and lesser size of the cirrus.     

The family Tetraonchidae (Monogenea): its structure and position among the monogeneans

The muscle fascicles of the haptor in Tetraonchus monenteron have been described. The muscle connection of the fan-shaped dorsal bars with dorsal anchors is shown. When these muscle fascicles are contracted the dorsal anchors works as pincers. The division of tetraonchids into two genera based on types of copulatory organs, morphology of bars and haptor ans associations with different groups of fishes is restored. Different authors based on ciliated cells and chaetotaxy of the oncomiracidium and comparative spermiogenetic of T. monenteron include the tetraonchids with 16 marginal hooks into the order Dactylogyroidea. In the same time, based on the analysis of the onthogenesis of the dactylogyrid's haptor they postulate, that the haptor of these worms originally had 2 pairs of anchors and only 14 marginal hooks. The present paper contains data indicating that different representatives of the Dactylogyridea have 14-18 marginal hooks. Author put forward a suggestion, that some group of dactylogyrids originally did not have the anchors.     

Neotropical Monogenoidea. 52. Diechodactylus joaberi n. g., n. sp. from the banded knifefish Gymnotus carapo (Gymnotiformes: Gymnotidae) in southeastern Brazil

Diechodactylus joaberi n. g., n. sp. is described from the body surface of the banded knifefish Gymnotus carapo L. (Gymnotiformes: Gymnotidae) from southeastern Brazil. The new genus is proposed to accommodate species with five pairs of hooks in anterior bilateral clusters on the haptor, three pairs of hooks in a single cluster on the posterior margin of the haptor, sclerites R1 associated with the superficial bar, and confluent intestinal caeca. The presence of five pairs of hooks in two bilateral clusters anterior in the haptor permits the differentiation of species of Diechodactylus from species of all known genera of the Gyrodactylidae. The genus is likely a member of a clade of the Gyrodactylidae comprising genera with a similar hook distribution.     

A new diplectanid (Monogenea) genus and species from the gills of the black snook, Centropomus nigrescens (Perciformes: Centropomidae) of the Pacific coast of Mexico

Cornutohaptor nigrescensi n. sp. (Diplectanidae) is described from the gills of the black snook, Centropomus nigrescens (Perciformes: Centropomidae) from the Pacific coast of Mexico. Cornutohaptor n. gen. is proposed for this new species and is characterized by possessing 2 intestinal ceca terminating blindly; a germarium looping right intestinal cecum; bilobed testis; 2 seminal vesicles; 7 pairs of hooks, each with protruding thumb; a grooved ventral bar and coiled male copulatory organ (MCO); an accessory piece comprising a "baglike structure" with an appendage; dorsal bars associated parallelly to body midline; and no adhesive accessory organs on the haptor. Cornutohaptor differs from all confamilial genera by including species with anchors with straight and deep root longest, hook pair 1 reduced in size, MCO with counterclockwise rings, and by the morphology of the accessory piece. Cornutohaptor nigrescensi most closely resembles species of Murraytrema Price, 1937, Lobotrema Tripathi, 1937, and Murraytrematoides Yamaguti, 1958, because of the absence of squamodiscs or lamellodiscs on the haptor and tegumental scales on the posterior portion of the body. Cornutohaptor differs from these genera in the position and number of haptoral bars (2 bars in Lobotrema spp., dorsal bars transversally associated in Murraytrema and Murraytrematoides spp.) and in having a coiled MCO (copulatory organ is a comparatively straight, poorly sclerotized tube in Murraytrematoides spp.). This is the first diplectanid described from a centropomid along the Pacific coast of Mexico.     

Calicobenedenia Polyprioni n. gen., n. sp. (Monogenoidea: Capsalidae) from the external surfaces of wreckfish, Polyprion americanus (Teleostei: Polyprionidae), in the north Atlantic

Calicobenedenia polyprioni n. sp. (Capsalidae) is described from the external surfaces (skin and eye) of wreckfish, Polyprion americanus (Teleostei, Perciformes, Polyprionidae), from the north Atlantic Ocean. The monotypic Calicobenedenia n. gen. is proposed for this species and is characterized, in part, by its members possessing an aseptate haptor armed with 14 submarginal hooks and 1 pair of anchors, a common genital pore opening marginally immediately posterior to the left cephalic lobe, 2 testes juxtaposed near the body midlength, and by lacking cephalic suckers or adhesive discs, accessory haptoral sclerites, and a uterine valve. The new genus most closely resembles Entobdella, which differs from Calicobenedenia by having an aseptate haptor armed with 14 submarginal hooks, 2 pairs of anchors, and a pair of accessary sclerites.     

Dactylogyrids (Monogenea: Dactylogyridea) with unusual number of the anchors, their origin and phylogenetic significance. Original data

The haptors Dactylogyrus spp., Anacanthorus sp., Trianchoratus sp. and Schilbetrematoides pseudodactylogyrus are investigated. On the base of the morphology, transfer of the domus, etc. a homology of the hooks in dactylogyrids (s. s.) and the pin-like structures (4 "A") in the haptor of Anacanthorinae and Dactylogyridae sensu Bychowsky et Nagibina, 1978 is demonstrated. The vestiges of the anchors in the haptor of dactylogyrids (s. l.), according to morphological data, correspond to the point of anchor formed during the ontogenesis. In S. pseudodactylogyrus the pins are redescribed as typical vestiges of the anchors.     

Gyrodactylus gvozdevi n. sp. (Gyrodactylidae: Monogenea) from Noemacheilus dorsalis (Kessler) in Kazakhstan

Gyrodactylus gvozdevi n. sp. (Gyrodactylidae: Monogenea) is described from the skin of the freshwater fish Noemacheilus dorsalis (Kessler) (Cobitidae: Cypriniformes) from Kazakhstan. This species is most closely related to G. pseudonemachili Ergens & Bykhovsky, 1967 in the shape and size of the anchors and both the ventral and dorsal bars, but can be distinguished from it by the shape and size of the hookproper of the marginal hooks.     

Neotropical Monogenoidea. 33. Three new species of Ancistrohaptor n. g. (Dactylogyridae,Ancyrocephalinae) on Triportheus spp. (Teleostei,Characidae) from Brazil,with checklists of ancyrocephalines recorded from neotropical characiform fishes

Three new species of Ancistrohaptor n. g. are described from the gills of three species of Triportheus (Characidae) collected from the environs of Manaus, Amazonas, Brazil: A. falcatum n. sp. from T. elongatus; and A. falciferum n. sp. and A. falcunculum n. sp. from T. angulatus, T. albus and T. elongatus. Ancistrohaptor n. g. is proposed for species possessing overlapping gonads, a dextral or dextroventral vaginal aperture, a coiled (counter-clockwise) male copulatory organ, two accessory pieces in the copulatory complex, and a haptor armed with two pairs of anchors (ventral anchor with elongate shaft), dorsal and ventral bars and 14 hooks; hook pair 1 (ventral) anterior to ventral bar, pairs 2–4 (ventral) lying bilaterally anterior to ventral anchor bases, pair 5 (ventral) associated with distal end of ventral anchor shafts, and pairs 6 and 7 (dorsal) bilateral about midway along haptoral length. Parasite-host and host-parasite lists of the Ancyrocephalinae from neotropical Characiformes are provided.     

A description of a new species Gyrodactylus moldovicus sp. n. (Monogenea: Gyrodactylidae) from the European mudminnow Umbra krameri Walbaum, 1792 from the lower Dnester basin

Gyrodactylus moldovicus sp. n. found on gills, body and in nasal cavities of the European mudminnow (Umbra krameri) differs from G. slovacicus Ergens, 1963 also living on the this host by bigger size of the body, anchors and marginal hooks; from G. cylindriformes Mueller et Van Cleave, 1932 living on the American mudminnow Umbra limi--by bigger size of the body; from G. limi Wood et Mizelle, 1957 also from U. limi--by the form of ventral and dorsal bars and form of marginal hooks. It differs from other freshwater gyrodactylids by special type of marginal hooks which have a hook-like end of the blade. Gyrodactylus moldovicus, G. slovacicus and G. limi have marginal hooks of quite different morphological types. By the morphology of anchors, ventral and sometimes dorsal bars and also morphology of cirrus, G. moldovicus is most related to three species from Cyprininae: G. stankovichi Ergens, 1970, G. longoacuminatus Zitnan, 1964 f. typica and G. shulmani Ling, 1962.     

Philureter trigoniopsis, a new genus and species (Dactylogyridae, Ancyrocephalinae) from the ureters and urinary bladder of Galaxias maculatus (Osmeriformes: Galaxiidae) in Patagonia (Argentina)

The monotypic Philureter n. gen. (Ancyrocephalinae; Dactylogyridae) is proposed to accommodate Philureter trigoniopsis n. sp. with the following features: presence of a cuplike ventral haptor armed with 14 hooks and 2 anchor/bar complexes; dorsal pair of anchors poorly defined and variable in shape, 1 frequently absent; tandem, intercecal gonads, testis bilaterally lobulated. Philureter trigoniopsis n. sp. is described from the ureters and urinary bladder of Galaxias maculatus (Jenyns, 1842) (Osmeriformes) in Patagonian Andean lakes, Argentina.     

A new Neocalceostomatid (Monogenoidea) from the gills of the blackfin sea catfish, Arius jella (Siluriformes: Ariidae), in the Bay of Bengal, India

Thysanotohaptor n. gen. (Neocalceostomatidae) is proposed to accommodate Thysanotohaptor rex n. sp. collected from the gills of the blackfin sea catfish Arius jella Day (Siluriformes: Ariidae) from off the coast of Visakhapatnam, Bay of Bengal, Andhra Pradesh, India. Thysanotohaptor is differentiated from the other known neocalceostomatid genera by its species having multiple postgermarial testes (single testis in species of Neocalceostoma and Neocalceostomoides ), lacking a transverse bar associated with the ventral anchor pair (present in species of Neocalceostoma ), and possessing a disc-shaped haptor with a pleated marginal frill (frill absent in Neocalceostomoides spp.; Neocalceostoma spp. with delicate marginal membranes). The Neocalceostomatidae is considered valid within the Order Dactylogyridea based on its members having a haptor armed with 10 marginal and 4 ventral hooks and a germarium having a distal loop prior to uniting with the ootype; the family is not assigned to a suborder of Dactylogyridea because of uncertainty in part about the way in which the distribution of haptoral hooks evolved within the taxon.     

Two new species of Cryptocephalum n. gen. (Monogenoidea: Dactylogyridae) from the cephalic lateral line of Percichthys trucha (Perciformes: Percichthyidae) in Patagonia, Argentina

Two new species of Monogenoidea were found parasitizing the cephalic lateral line canals of Percichthys trucha (Valenciennes) (Perciformes: Percichthyidae). These species are described as members of a newly proposed genus of Dactylogyridae. Cryptocephalum n. gen. is characterized by the site of infection and the combination of the several features: ventral and dorsal anchor/bar complexes, anchors with strongly elongated shaft and recurved point, shaft and point of dorsal anchors protruding laterally from haptor, hooks with 2 subunits and with pair 5 smaller than the others; gonads overlapping; coiled male copulatory organ with counterclockwise rings, accessory piece formed by 2 distinct parts, and a tubular, sclerotized ventral vagina. C ryptocephalum petreum n. sp. is characterized by having both anchor pairs protruding laterally from haptor, male copulatory organ with a coil of 2-1/2 rings, accessory piece tweezers-shaped, and sclerotized vaginal vestibule. Cryptocephalum spiralis n. sp. has ventral anchors protruding ventrally and dorsal ones protruding laterally, male copulatory organ with a coil of 1-1/2 rings, the antero-dorsal part of the accessory piece saddle-shaped, vaginal vestibule not present, and coiled vagina. This is the first record of Dactylogyridae species parasitizing the cephalic lateral line of fishes.     

Origin and evolution of the hamuli in the monogeneans

The hypothesis of the origin and evolution of the hamuli in monogeneans is proposed. It is suggested that the hamuli originated as the adult attachment organs of protomonogeneans inhabited the gills of the first vertebrates. Primarily they were represented by two lateral pairs of large hooks disposed anterior to the larval haptor. The fundamental direction in the evolution of monogeneans was the concentration of all attachment structures on the growing haptor. It the course of this evolutionary process, the hamuli onchoblasts migrated to the haptor, in which they had reached the position in the hind part of the haptor. The neotenic evolution of the Dactylogyridea and Gyrodactyloidea resulted in the forming new hamuli pairs. The hooks of opposite sides of the haptor are joined in a single complex within each side by the transverse plates (bars). So the presence of 4 hamuli is plesiomorphy for all the monogeneans and the presence of the transverse bars and new hamuli pairs are apomorphy for the Dactylogyridea and Gyrodactyloidea, whose evolution was linked with that of the Teleostei. The origin of the new hamuli pairs and transverse bars in the Dactylogyridea and Gyrodactyloidea appears to be a convergence.     

On the ontogeny of the haptor and the evolution of the Monogenea

Data on the ontogeny of the posterior haptor of monogeneans were obtained from more than 150 publications and summarised. These data were plotted into diagrams showing evolutionary capacity levels based on the theory of a progressive evolution of marginal hooks, anchors and other attachment components of the posterior haptor in the Monogenea (Malmberg, 1986). 5 + 5 unhinged marginal hooks are assumed to be the most primitive monogenean haptoral condition. Thus the diagrams were founded on a 5 + 5 unhinged marginal hook evolutionary capacity level, and the evolutionary capacity levels of anchors and other haptoral attachement components were arranged according to haptoral ontogenetical sequences. In the final plotting diagram data on hosts, type of spermatozoa, oncomiracidial ciliation, sensilla pattern and protonephridial systems were also included. In this way a number of correlations were revealed. Thus, for example, the number of 5 + 5 marginal hooks correlates with the most primitive monogenean type of spermatozoon and with few sensillae, many ciliated cells and a simple protonephridial system in the oncomiracidium. On the basis of the reviewed data it is concluded that the ancient monogeneans with 5 + 5 unhinged marginal hooks were divided into two main lines, one retaining unhinged marginal hooks and the other evolving hinged marginal hooks. Both main lines have recent representatives at different marginal hook evolutionary capacity levels, i.e. monogeneans retaining a haptor with only marginal hooks. For the main line with hinged marginal hooks the name Articulon-choinea n. subclass is proposed. Members with 8 + 8 hinged marginal hooks only are here called Proanchorea n. superord. Monogeneans with unhinged marginal hooks only are here called Ananchorea n. superord. and three new families are erected for its recent members: Anonchohapteridae n. fam., Acolpentronidae n. fam. and Anacanthoridae n. fam. (with 7 + 7, 8 + 8 and 9 + 9 unhinged marginal hooks, respectively). Except for the families of Articulonchoinea (e.g. Acanthocotylidae, Gyrodactylidae, Tetraonchoididae) Bychowsky's (1957) division of the Monogenea into the Oligonchoinea and Polyonchoinea fits the proposed scheme, i.e. monogeneans with unhinged marginal hooks form one old group, the Oligonchoinea, which have 5 + 5 unhinged marginal hooks, and the other group form the Polyonchoinea, which (with the exception of the Hexabothriidae) has a greater number (7 + 7, 8 + 8 or 9 + 9) of unhinged marginal hooks. It is proposed that both these names, Oligonchoinea (sensu mihi) and Polyonchoinea (sensu mihi), will be retained on one side and Articulonchoinea placed on the other side, which reflects the early monogenean evolution. Except for the members of Ananchorea [Polyonchoinea], all members of the Oligonchoinea and Polyonchoinea have anchors, which imply that they are further evolved, i.e. have passed the 5 + 5 marginal hook evolutionary capacity level (Malmberg, 1986). There are two main types of anchors in the Monogenea: haptoral anchors, with anlages appearing in the haptor, and peduncular anchors, with anlages in the peduncle. There are two types of haptoral anchors: peripheral haptoral anchors, ontogenetically the oldest, and central haptoral anchors. Peduncular anchors, in turn, are ontogenetically younger than peripheral haptoral anchors. There may be two pairs of peduncular anchors: medial peduncular anchors, ontogentically the oldest, and lateral peduncular anchors. Only peduncular (not haptoral) anchors have anchor bars. Monogeneans with haptoral anchors are here called Mediohaptanchorea n. superord. and Laterohaptanchorea n. superord. or haptanchoreans. All oligonchoineans and the oldest polyonchoineans are haptanchoreans. Certain members of Calceostomatidae [Polyonchoinea] are the only monogeneans with both (peripheral) haptoral and peduncular anchors (one pair). These monogeneans are here called Mixanchorea n. superord. Polyonchoineans with peduncular anchors and unhinged marginal hooks are here called the Pedunculanchorea n. superord. The most primitive pedunculanchoreans have only one pair of peduncular anchors with an anchor bar, while the most advanced have both medial and lateral peduncular anchors; each pair having an anchor bar. Certain families of the Articulonchoinea, the Anchorea n. superord., also have peduncular anchors (parallel evolution): only one family, the Sundanonchidae n. fam., has both medial and lateral peduncular anchors, each anchor pair with an anchor bar. Evolutionary lines from different monogenean evolutionary capacity levels are discussed and a new system of classification for the Monogenea is proposed.In agreeing to publish this article, I recognise that its contents are controversial and contrary to generally accepted views on monogenean systematics and evolution. I have anticipated a reaction to the article by inviting senior workers in the field to comment upon it: their views will be reported in a future issue of this journal. EditorIn agreeing to publish this article, I recognise that its contents are controversial and contrary to generally accepted views on monogenean systematics and evolution. I have anticipated a reaction to the article by inviting senior workers in the field to comment upon it: their views will be reported in a future issue of this journal. Editor     

Lamellodiscus euzeti n. sp. (Monogenea:Diplectanidae), a parasite from Dentex canariensis and D. gibbosus (Teleostei:Sparidae) in the Atlantic Ocean and Mediterranean Sea

Lamellodiscus euzeti n. sp. (Monogenea:Diplectanidae) is described from the gills of two sparid fishes, Dentex canariensis (Steindachner) off Senegal and Ivory Coast and D. gibbosus (Rafinesque) off Senegal and Tunisia. The new species belongs to the "ignoratus" group, characterized by a lamellodisc with complete lamellae, a "lyre" shaped male copulatory organ type, and the "ignoratus" sensu stricto subgroup, characterized by a haptor with simple lateral dorsal bars. Lamellodiscus euzeti n. sp can be distinguished from all the congeneric species of the "ignoratus" subgroup by the presence of a prominent protuberance at the base of the curved part of the simple piece of the male copulatory organ (MCO), a large bulb at the base of the bifurcated piece of the MCO and the presence of 5-6 spines in the distal portion of the axial branch of the bifurcated piece of the MCO. Specificity and biogeography of Lamellodiscus species from sparid fishes are discussed.     

A new monogenean genus from an ephippid fish off Peninsular Malaysia

Sundatrema langkawiense n. g., n. sp. (Monogenea: Ancyrocephalidae) is described from the gills of the orbfish Ephippus orbis (Bloch) (Ephippidae) off the Island of Langkawi, Malaysia, in the Andaman Sea. This new genus has the ancyrocephalid characteristics of four anchors, 14 marginal hooks and two bars, but differs from other four-anchored monogenean genera, and notably from Parancylodiscoides Caballero & Bravo Hollis, 1961 (found on the ephippids Chaetodipterus spp. off Central and South America), by having a unique combination of features. These include a muscular genital sucker and a vas deferens and vagina on the same (sinistral) side of the body. It is similar to Parancylodiscoides in having four haptoral reservoirs opening at the anchoral apertures, four anchors, similar connecting bars and small marginal hooks. The new species is characterised by the above generic features and by possessing a small, short copulatory organ lacking an accessory piece. Diplectanum longiphallus MacCallum, 1915 (previously attributed to Ancyrocephalus Creplin, 1839, Tetrancistrum Goto & Kikuchi, 1917 and Pseudohaliotrema Yamaguti, 1953) is transferred to Parancylodiscoides as P. longiphallus (MacCallum, 1915) n. comb.     

海南岛海水鱼类单殖吸虫研究及宽海盘虫二新种记述

记述了采自海南岛后水湾的眶棘双边鱼Ambassis gymnocephalus Lacépéde鳃上寄生的宽海盘虫2新种.张氏宽海盘虫Euryhaliotrema zhangjianyingi sp nov.以其边缘小钩明显长于两对中央大钩,支持器的套环状特殊结构,两对中央大钩和联结片而不同于属内的已知种;双边鱼宽海盘虫,Euryhaliotrema ambassisi sp.nov.以其交接器的量度,后吸器中央大钩内突基部较宽,外突较小,钩基部较直,钩尖短而不同于相似种和属内已知种.文中量度μm,模式标本保存在海南师范学院生物系.