Revision of Parancylodiscoides Caballero y C. & Bravo-Hollis, 1961 (Monogenoidea: Dactylogyridae), with a redescription of P. longiphallus (MacCallum, 1915) from the Atlantic spadefish Chaetodipterus faber (Broussonet) (Acanthuroidei: Ephippidae) in the Gulf of Mexico

The generic diagnosis of Parancylodiscoides Caballero y C. & Bravo-Hollis, 1961 (Monogenoidea: Dactylogyridae), with three valid species, was amended to include dactylogyrids having: a haptor with dorsal and ventral anchor/bar complexes, 14 hooks (seven pairs) and four reservoirs (two pairs); a dorsal bar with bifurcate ends; hooks with protruding, blunt and slightly depressed thumbs and undilated shanks; a dextroventral vaginal aperture leading to an elongate and oblique vaginal vestibule; a germarium dextral to the testis; a vas deferens looping the left intestinal caecum; a copulatory complex lacking an accessory piece; and two intestinal caeca lacking diverticula and united posterior to the gonads. Parancylodiscoides is most similar to Sundatrema Lim & Gibson, 2009, from which it differs only by the position of the vaginal aperture (sinistroventral in Sundatrema spp.) and by lacking a sucker-like genital pore. New information concerning the number and distribution of haptoral hooks, the relative positions of the gonads and the course of the vas deferens was provided for the type-species, P. chaetodipteri Caballero y C. & Bravo-Hollis, 1961. Parancylodiscoides longiphallus (MacCallum, 1915) Lim & Gibson, 2009 was redescribed based on specimens collected from the Atlantic spadefish Chaetodipterus faber from the Gulf of Mexico off Mississippi and Guaratuba Bay, Paraná, Brazil; its occurrence on the Atlantic spadefish from the Gulf of Mexico, Guaratuba Bay and off Puerto Rico represented new geographical records for this helminth. Parancylodiscoides caballerobravorum Cezar, Luque & Amato, 1999 was considered a junior subjective synonym of P. longiphallus. The monotypic Isohaliotrema Young, 1968 was placed in synonymy with Parancylodiscoides and its type-species, I. platacis Young, 1968, transferred to Parancylodiscoides as Parancylodiscoides platacis (Young, 1968) n. comb.     

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.     

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     

Seasonal variations of the opisthaptoral hard parts of Gyrodactylus derjavini Mikailov, 1975 (Monogenea: Gyrodactylidae) on brown trout Salmo trutta L. parr and Atlantic salmon S. salar L. parr in the River Sandvikselva,Norway

Seasonal variations in the size and shape of the marginal hooks, anchors and ventral bar of the opisthaptor of Gyrodactylus derjavini Mikailov, 1975 were studied. The G. derjavini specimens were collected from brown trout Salmo trutta L. parr and Atlantic salmon S. salar L. parr in the River Sandvikselva, southeastern Norway. Samples were taken at roughly monthly intervals during a 13-month period. The marginal hooks, anchors and ventral bars showed considerable seasonal variation in size, but varied very little in shape. The size increased when the water temperature decreased and vice versa.     

Gyrodactylus anarhichatis n. sp. and G. microanchoratus n. sp. (Monogenea: Gyrodactylidae) from the Atlantic wolf-fish Anarhichas lupus (Anarhichadidae) off the coast of Norway

The gyrodactylid monogeneans Gyrodactylus anarhichatis n. sp. and G. microanchoratus n. sp. are reported from the skin and fins of wild Atlantic wolf-fish Anarhichas lupus L. caught off the coast of northern Norway. G. anarhichatis n. sp. is also reported from farmed Atlantic wolf-fish and spotted wolf-fish A. minor Olafsen. G. anarhichatis n. sp. most closely resembles G. corti Mizelle & Kritsky, 1967, but is also similar to G. perlucidus Bychowsky & Poljansky, 1953 and G. errabundus Malmberg, 1970, while G. microanchoratus n. sp. differs from most other Gyrodactylus spp. by having marginal hooks longer than anchors and a peculiar lump on the marginal hook sickle toe pointing towards the sickle point.     

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.     

Seasonal variations of opisthaptoral hard parts of Gyrodactylus salaris Malmberg, 1957 (Monogenea: Gyrodactylidae) on parr of Atlantic salmon Salmo salar L. in the River Batnfjordselva,Norway

Seasonal variations in size and shape of the marginal hooks, the anchors and the ventral bar of the opisthaptor of Gyrodactylus salaris Malmberg, 1957 were studied. The G. salaris specimens were collected from parr of Atlantic salmon Salmo salar L. in the River Batnfjordselva, north-western Norway. Samples were taken at roughly monthly intervals during a two-year period. The marginal hooks, the anchors and the ventral bar showed considerable seasonal variation in size, but varied only slightly in shape. The variation in 12 of the 14 characters measured showed a significant regression to the variation in the water temperature. The total length of the marginal hooks of G. salaris can be considerably longer than the previously reported maximum of 40 m for the species.     

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.     

Automated identification of Monogeneans using digital image processing and K-nearest neighbour approaches

Background

Monogeneans are flatworms (Platyhelminthes) that are primarily found on gills and skin of fishes. Monogenean parasites have attachment appendages at their haptoral regions that help them to move about the body surface and feed on skin and gill debris. Haptoral attachment organs consist of sclerotized hard parts such as hooks, anchors and marginal hooks. Monogenean species are differentiated based on their haptoral bars, anchors, marginal hooks, reproductive parts’ (male and female copulatory organs) morphological characters and soft anatomical parts. The complex structure of these diagnostic organs and also their overlapping in microscopic digital images are impediments for developing fully automated identification system for monogeneans (LNCS 7666:256-263, 2012), (ISDA; 457–462, 2011), (J Zoolog Syst Evol Res 52(2): 95–99. 2013;). In this study images of hard parts of the haptoral organs such as bars and anchors are used to develop a fully automated identification technique for monogenean species identification by implementing image processing techniques and machine learning methods.

Result

Images of four monogenean species namely Sinodiplectanotrema malayanus, Trianchoratus pahangensis, Metahaliotrema mizellei and Metahaliotrema sp. (undescribed) were used to develop an automated technique for identification. K-nearest neighbour (KNN) was applied to classify the monogenean specimens based on the extracted features. 50% of the dataset was used for training and the other 50% was used as testing for system evaluation. Our approach demonstrated overall classification accuracy of 90%. In this study Leave One Out (LOO) cross validation is used for validation of our system and the accuracy is 91.25%.

Conclusions

The methods presented in this study facilitate fast and accurate fully automated classification of monogeneans at the species level. In future studies more classes will be included in the model, the time to capture the monogenean images will be reduced and improvements in extraction and selection of features will be implemented.

     

Neocalceostoma Tripathi, 1957 and Neocalceostomoides Kritsky,Mizelle & Bilqees, 1978 (Monogenea: Neocalceostomatidae n. fam.) from ariid fishes of Peninsular Malaysia

Three new species of Neocalceostomoides Kritsky, Mizelle & Bilqees, 1978 and Neocalceostoma elongatum Tripathi, 1957 were found on five species of Arius from Peninsular Malaysia. N. elongatum was collected from Arius sagor. A. venosus and A. maculatus, whereas Neocalceostomoides spinivaginalis n. sp., N. hamatum n. sp. and N. simplex n. sp. were obtained from A. thalassinus, A. sagor and A. caelatus, respectively. The three new species of Neocalceostomoides are similar to Neocalceostoma elongatum in the morphology of the soft anatomical parts and in having 14 marginal hooks, but differ in having the two anchors situated far apart without a connecting bar. The possibility that Neocalceostomoides and Neocalceostoma are synonymous is noted. The generic diagnosis of Neocalceostomoides is amended herein and a new family, the Neocalceostomatidae, is proposed to accommodate Neocalceostoma and Neocalceostomoides.     

<Emphasis Type="Italic">Diplectanocotyla</Emphasis> Yamaguti, 1953 (Monogenea: Diplectanoidea) from <Emphasis Type="Italic">Megalops cyprinoides</Emphasis> (Broussonet) (Teleostei: Megalopidae) off Peninsular Malaysia

Two known and two new species of Diplectanocotyla Yamaguti, 1953 (D. gracilis Yamaguti, 1953, D. megalopis Rakotofiringa & Oliver, 1987, D. langkawiensis n. sp. and D. parva n. sp.) were collected from Megalops cyprinoides (Megalopidae) off Langkawi, Kedah and Matang, Perak, Peninsular Malaysia. All four species possess similar types of sclerotised male and female reproductive structures and similar soft anatomical features. The squamodisc sclerites of all four species have spine-like projections with varying degrees of visibility and shapes (sharp-pointed to triangular). In D. megalopis and D. langkawiensis n. sp. the spines are sharp-pointed and distinct on sclerites from rows 5–6 onwards. In D. gracilis and D. parva n. sp. the sclerite spines are triangular, lightly sclerotised and occur on almost all of the sclerites. D. parva n. sp. has comparatively the smallest set of anchors, bars, squamodiscs and squamodisc suckers. The anchors and bars of the other three species are almost similar in overall size, and the main distinguishing feature is the relative lengths of the inner and outer roots of the ventral anchors. In D. gracilis the outer root is very much smaller than the inner root and they are disposed almost at a right angle to each other. In D. megalopis the outer root is usually about half the length of the inner root and the roots are inclined at c.60° to each other. In D. langkawiensis n. sp. the roots are inclined at c.40° degrees and the outer root is of a similar length or only slightly shorter than the inner root. The openings of the two squamodisc suckers of all four Diplectanocotyla species are surrounded by tiny scale-like spines. Bifid tegumental spines are found in the posterior region of all four species, differing only in their extent: in D. parva n. sp. the tegumental spines are only distributed in the peduncular region and not beyond, whilst in the other three species the tegumental spines extend from the posterior level of the testis to the end of the peduncle. An amended diagnosis of Diplectanocotyla and a key to its species are appended.     

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.     

A new genus and three new species of dactylogyrids (Monogenea), gill parasites of the threadfin bass,Pronotogrammus multifasciatus Gill (Perciformes: Serranidae) in the Southeastern Pacific Ocean off Peru

Pronotogrammella n. g. is erected to accommodate Pronotogrammella boegeri n. sp. (type-species), Pr. scholzi n. sp. and Pr. multifasciatus n. sp. (Monogenea: Dactylogyridae). The new species are gill parasites of the threadfin bass Pronotogrammus multifasciatus Gill (Perciformes: Serranidae), a demersal teleost collected from off the coastal zone of Puerto Pizarro, Tumbes, Peru. Pronotogrammella n. g. is mainly characterised by having broadly fork-shaped dorsal anchors, which have an accessory anchor sclerite articulated to the tip of the superficial roots. Pronotogrammella n. g. is also characterised by having: (i) a tubular tapered-shaped male copulatory organ (MCO), filamentous distally, with a clockwise coil at distal end or not, lacking accessory piece; (ii) a dorsal bar with an anteromedial delicate umbelliform membrane supported by two processes; (iii) hooks with upright blunt thumb and uniform shank; (iv) a vaginal aperture dextrolateral; (v) a subquadrangular haptor, with inconspicuous lateral flaps and lacking haptoral reservoirs; and (vi) eye-spot or chromatic granules absent. Pronotogrammella boegeri n. sp. is characterised by its crosier-shaped MCO having a clockwise coil at distal end and by its dorsal bar with a straight anteromedial processes. Pronotogrammella scholzi n. sp. is typified by possessing of a dorsal bar with the anteromedial processes like cow horns, hoof-shaped deep roots of the dorsal anchors and a broader shaft of the MCO. Pronotogrammella multifasciatus n. sp. differs from all congeners by having a tubular MCO with twisted shaft and a base with a short and broad arm and by having an almost dumbbell-shaped ventral bar.

     

Species of <Emphasis Type="Italic">Neohaliotrema</Emphasis> Yamaguti, 1965 (Monogenea: Ancyrocephalidae) from the pomacentrid <Emphasis Type="Italic">Abudefduf vaigensis</Emphasis> (Quoy &; Gaimard) off Pulau Langkawi,Malaysia, with a revised diagnosis of the genus and a key to its species

Four new and one unidentified species of Neohaliotrema Yamaguti, 1965 were obtained from the gills of the Indo-Pacific sergeant Abudefduf vaigensis (Quoy & Gaimard) off Pulau Langkawi, Malaysia. The five species, N. malayense n. sp., N. bombini n. sp., N. andamanense n. sp., N. parvum n. sp. and an unidentified Neohaliotrema sp. (similar to N. macracanthum Zhukov, 1976), are described and distinguished based mainly on features of the haptor. Species of this genus are divisible into two groups, the ‘maomao group’, with two pairs of morphometrically modified ‘marginal’ hooks and a fenestrated haptor, and the ‘gracile group’, with morphologically similar marginal hooks and an entire haptor. With the exception of N. bombini n. sp., the species described fit within the ‘maomao group’. It is suggested that the more complex Neohaliotrema species of the ‘maomao group’ have modified hooks 1 and 2 on a haptoral ‘isthmus’ between two large apertures, i.e. ‘windows’, whereas the less complex species lacking these features are those of the ‘gracile group’. Neohaliotrema spp. have only a single pair of pigmented eye-spots. A fenestrated haptor is unique to the Neohaliotrema spp. of the ‘maomao group’. The generic diagnosis of Neohaliotrema is amended to include new data and a key to its known species is presented.     

Chimaerarhynchus n. g. andPatellobothrium n. g., two new genera of trypanorhynch cestodes with unique poeciloacanthous armatures,and a reorganisation of the poeciloacanthous trypanorhynch families

Chimaerarhynchus rougetae n. g., n. sp. is described fromSqualus acanthias andCentrophorus sp. from the coast of Senegal, and differs from all other trypanorhynch genera in having a chainette composed of dissimilar elements, that is, double-winged hooks alternating with pairs of hooks each with a single lateral wing. The new genus is allocated to the Gymnorhynchidae Dollfus, 1935.Patellobothrium quinquecatenatum n.g., n. sp. is described from the spiral intestine ofSphyrna mokarran from Darwin, Northern Territory, Australia and plerocerci fromRachycentron canadus from Queensland, Australia. The genus is distinguished from all others in possessing five chainettes. It is allocated to the family Mustelicolidae Dollfus, 1969. The relationships of all genera of trypanorhynchs possessing chainettes are discussed, and they are divided into three groups: (1) Dasyrhynchidae Dollfus, 1935, Lacistorhynchidae Guiart, 1927, Mustelicolidae and Hornelliellidae Yamaguti, 1954 are considered closely related since all genera possess two bothridia, a hermaphroditic duct and have hollow hooks; (2) Gymnorhynchidae, amended to contain onlyGymnorhynchus Rudolphi, 1819 andChimaerarhynchus n.g., is distinct in possessing four bothridia, an accessory seminal vesicle and hollow hooks; (3) Mixodigmatidae Dailey & Vogelbein, 1982, amended to includeMixodigma Dailey & Vogelbein, 1982 andHalysiorhynchus Pintner, 1913 has four bothridia, lacks seminal vesicles and a hermaphroditic duct and has solid hooks.A new family Molicolidae n. fam. is erected forMolicola Dollfus, 1935 andStragulorhynchus Beveridge & Campbell, 1988. The new family has a poeciloacanthous armature, and is distinguished by possessing a band of hooks on the external surface of the tentacle, four sessile bothridia and an acessory seminal vesicle.Myrmillorhynchus Bilqees, 1980 is suppressed as a synonym ofPterobothrium Diesing, 1850.Neogymnorhynchus Bilquees & Shah, 1982, is suppressed as a synonym ofPterobothrium, with the type species,N. platycephali becoming a synonym ofP. heteracanthum Diesing, 1850.Eulacistorhynchus Subhapradha, 1957 is considered agenus inquirendum;Gymnorhynchus cymbiumi Chincholikar & Shinde, 1977 is also a synonym ofPterobothrium heteracanthum Diesing, 1850.     

Dactylogyridae (Monogenea) from the gills of Iheringichthys labrosus (Osteichthyes: Pimelodidae) from the upper Paraná River floodplain,Brazil, with the proposal of Pseudovancleaveus n. g

Two new species of Demidospermus Suriano, 1983 and a new genus, Pseudovancleaveus, and species are described from the gills of Iheringichthys labrosus (Pimelodidae). The fishes were collected from the upper Paraná River floodplain, Brazil. D. mandi n. sp. is characterised by the distal region of the copulatoty organ having an expanded bulb and D. labrosi n. sp. by the copulatory organ having a funnel-shaped proximal extremity. The latter species also has an accessory piece comprising a variable sheath enclosing the distal shaft of the copulatory organ and two anterolateral structures resembling irregular spheres. Pseudovancleaveus paranaensis. n. g., n. sp. is characterised by a sinistral vagina, overlapping gonads, a copulatory ligament, anchors without a fold on the base and hooks with slightly inflated shanks. A new combination, Pseudovancleaveus platensis, is proposed for Vancleaveus platensis Suriano & Incorvaia, 1995.     

A special technique for studying haptoral sclerites of monogeneans

The marginal hooks and anchors have been digested from the haptors of the monogeneans Gyrodactylus salaris and Discocotyle sagittata. These structures then can be measured and drawn more accurately than those surrounded by haptoral tissue. The technique also facilitates the study of isolated hooks with SEM. The results of studies using this digestion technique are presented.     

Three new species of Dactylogyrus Diesing, 1850 (Monogenea: Dactylogyridae) from the gills of the bala sharkminnow Balantiocheilos melanopterus (Cyprinidae) from Thailand

Three new species of Dactylogyrus are described from the gills of the cyprinid fish Balantiocheilos melanopterus (Bleeker) imported from Thailand via the aquarium trade. They are D. coartatus n. sp., D. macrocolpius n. sp. and D. melanopteri n. sp. The double-bar species, D. coartatus n. sp. and D. melanopteri n. sp., are characterised by hooks that are markedly large in relation to the size of the anchors. Clip-like anchors with a sharply recurved, long point are a unique feature of D. coartatus n. sp. The single-bar species, D. macrocolpius n. sp., is characterised by having a copulatory organ composed of a spiral copulum and a medial accessory piece with thorns.     

<Emphasis Type="Italic">Empruthotrema longipenis</Emphasis> n. sp. (Monogenoidea: Monocotylidae: Merizocotylinae) from the olfactory sacs of the smooth butterfly ray <Emphasis Type="Italic">Gymnura micrura</Emphasis> (Bloch &amp; Schneider) (Myliobatiformes: Gymnuridae) in the Gulf of Mexico

A new species of Empruthotrema Johnston & Tiegs, 1922 is described based on specimens collected from the olfactory sacs of smooth butterfly rays Gymnura micrura (Bloch & Schneider) captured in Mobile Bay (northcentral Gulf of Mexico), Alabama, USA. Empruthotrema longipenis n. sp. is most similar to the type-species Empruthotrema raiae (MacCallum, 1916) Johnston & Tiegs, 1922 by having 12 marginal and two interhamular loculi with members of haptoral hook pair 1 located midway along the periphery of each interhamular loculus and those of hook pair 2 located at the marginal termini of the bilateral septa flanking the interhamular loculi. Empruthotrema longipenis n. sp. differs from E. raiae by having a much longer male copulatory organ and from its remaining congeners by the sinistral and extracecal ejaculatory bulb flanking the pharynx, the number of interhamular and marginal septa, and the distribution of hook pairs 1 and 2 along the haptoral margin. This is the first report of a monocotylid from the smooth butterfly ray and from Mobile Bay. The diversity of haptoral morphotypes among the currently accepted species of Empruthotrema is detailed and discussed in the context of monophyly of the genus.