Hysterothylacium Ward and Magath 1917
Notice bibliographique
Résumé
Hysterothylacium Ward and Magath, 1917 Synonyms: Thynnascaris Dollfus, 1933; Contracaecum (Thynnascaris) Dollfus 1935; Contracaecum (Erschovicaecum) Mozgovoi, 1951; Contracaecum (Simplexonema) Kreis, 1952 nom. nud.; Iheringascaris Pereira, 1935; Contracaecum (Acollaris) Araujo, 1970 Generic diagnosis (after Deardorff & Overstreet 1981). Raphidascaridinae. Body elongate, reaching greatest width near midbody. Cuticle with annulations moderately or weakly defined or lacking (presumably unreported). Cuticular alae distinct or indistinct. Lips approximately equal in size, usually wider than long, bearing transparent cuticular flanges on lateral margins: flanges with or without indentations; internal pulp usually pedunculated; dorsal lip with two lateral doubled papillae; subventral lips with amphid, adjacent mediolateral doubled papilla, and single lateral papilla. Dentigerous ridges absent. Interlabia present. Interlabial grooves present or absent. Ventriculus almost spherical; ventricular appendix sac-like or cylindrical, with septum dividing structure into two equal longitudinal pouches; intestinal caecum usually shorter than ventricular appendix. Excretory system with excretory pore at or near nerve ring level, with duct extending to at least left lateral cord. Rectal glands present or absent (presumably unreported). Spicules similar, alate, equal or slightly unequal in length. Gubernaculum absent. Vulva anterior to midbody. Uterus didelphic, opisthodelphic. Tail conical, tip with or without spines. Medioventral pre-cloacal organ usually distinct on pre-cloacal fold. Phasmids usually distinct. Parasites of marine, estuarine and fresh-water fishes. Comments: Gopar-Merino et al. (2005) claimed that 61 species of Hysterothylacium have been recognized; however, there are more than 61species if “morphospecies”, “sibling species” and “cryptic species” are taken into account. According to Rye & Baker (1992) most Hysterothylacium species occur in the alimentary tract of marine fishes rather than fresh-water ones. In common with some other aquatic ascaridoids, species of Hysterothylacium have evolved remarkable flexibility in completing the life-cycle. For example, Luque et al. (2007) reported L4 of Hysterothylacium sp. in the haemocoel of amphipods, Paracorophium excavatum, from New Zealand waters. Furthermore, several of the adult males showed precocious sexual development, having undergone the 3rd and 4th (final) moults in the amphipod host. Moreover, H. haze also departs from the life-cycle known for many other species. Yoshinaga et al. (1989) studied natural and experimental infections of H. haze in gobies Acanthogobius flavimanus from Tokyo Bay, concluding that the life-cycle may be direct and involve invertebrates as paratenic hosts; this life-cycle might represent an example of extreme precocity in which the fish intermediate host has also become a final host (Anderson 1998). Like Contracaecum and Phocascaris (see above) the genus Hysterothylacium is defined by characteristics of the adults, and agreeing again with Moravec (2013) it is difficult to assign larvae to any one species. It is not possible to design a key for their reliable identification, and the following keys are for the identification of the adults only. Feeding experiments to rear larvae to adults and the application of molecular markers to identify species may be solutions to this and similar problems. Several taxa are considered and, where possible, described, their names having appeared in the relevant Canadian literature. Only two Hysterothylacium species (** H. analarum and ** H. brachyurum) are known from Canadian fresh-water fishes. While four species (** H. aduncum, H. corrugatum, H. incurvum and H. reliquens) have been reported from Canadian marine fishes, only ** H. aduncum is abundant, having been recorded from a wide variety of fish species. In contrast, there is only one report, that of Hogans et al. (1983), for each of the other three Hysterothylacium species. All of the specimens were recovered from the stomachs of swordfish, Xiphias gladius, collected from the “northwest Atlantic Ocean”. The coordinates for the collection site(s) are not given but it may be assumed that these were within Canadian waters, so the descriptions are given below. Swordfish are oceanic travellers that enter Canadian waters usually about June and leave in October and November. They move through a great range of depths, feeding on various fish species and shortfin squid, Illex illecebrosus (Scott and Scott 1988). It is possible, therefore, that infections with the three species of Hysterothylacium were acquired by swordfish at locations remote from Canadian waters. It is worth noting that Hogans et al. (1983) deposited representative specimens of each nematode species (and of the other helminths collected) at a public museum and provided catalogue numbers; details may be found in the original paper. While two other species of Hysterothylacium, H. magnum and H. melanogrammi, have been recorded from Canadian marine fishes the species are of doubtful validity, as discussed below.
Récupéré en direct depuis OpenAlex et désinversé. Les résumés ne sont pas conservés dans cette base de données : les index inversés représentent 8,6 Go des 9,3 Go de texte de la base, et le serveur dispose de 13 Go libres.
Comment cette classification a été obtenuedéplier
Prédiction machine sur la base complète
Imitation des enseignantsNi prévalence calibrée, ni vérité terrain. Validation humaine à venir. Le volet Gemma est une étiquette directe du modèle pour chaque travail de la base, lue sur la notice réduite au titre. Le volet Codex est un classifieur appris des 10 348 étiquettes directes de Codex et calibré sur les taux pondérés de l'échantillon; les champs sans appui suffisant ne portent aucun appel Codex. Le mode candidate est l'union des deux volets; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont pas des étiquettes humaines.
Scores du classifieur distillé par catégorie (deux têtes)
| Catégorie | Codex | Gemma |
|---|---|---|
| Métarecherche | 0,000 | 0,000 |
| Méta-épidémiologie (sens strict) | 0,000 | 0,000 |
| Méta-épidémiologie (sens large) | 0,000 | 0,000 |
| Bibliométrie | 0,001 | 0,001 |
| Études des sciences et des technologies | 0,001 | 0,000 |
| Communication savante | 0,000 | 0,001 |
| Science ouverte | 0,000 | 0,001 |
| Intégrité de la recherche | 0,001 | 0,000 |
| Charge utile insuffisante (le modèle a refusé de juger) | 0,010 | 0,004 |
Scores machine (provisoires)
Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.
Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.
score_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découleClassification
machine, non validéePrédiction automatique; un appel candidat d’une seule source (Gemma direct ou Codex distillé), pas un consensus.
Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».