Glypthelmins intestinalis Lucker 1931
Notice bibliographique
Résumé
Glypthelmins intestinalis (Lucker, 1931), O´ Grady, 1987 (Figs. 12–15) Synonyms Haplometrana intestinalis Lucker, 1931: 1 –7. Figs. 1–4; Haplometrana utahensis, Olsen, 1937b: 13 –28 (Description and life cycle); Waitz (1959: 385–387) [Sinonimizes Haplometrana utahensis with Haplometrana intestinalis]; Haplometrana intestinalis, Brooks, 1977; Glypthelmins intestinalis, O´ Grady (1987: 52) [Transfers Haplometrana intestinalis to Glypthelmins intestinalis]. Haplometrana intestinalis, Rannala (1990: 746–747) [Alozyme study]; Rannala (1991: 805–808) [Alozyme study]; Rannala (1992: 993 –1000) [Alozyme study]. Taxonomic summary Type-host: Rana pretiosa. Habitat: Intestine. Type-locality: Bothell, King County, Washington, U.S.A. Type specimens deposition: USNPC 29903. Diagnosis: This species can be differentiated by the following unique traits: Body filiform with a ratio of body width/length longer than 7; esophagus longer than the ventral sucker; suctorial disc present on the ventral sucker; testes located in tandem; vitelline follicles extend from the ovarian region to the beginning of the last third of the body. Vitelline follicles are confluent in the post-testicular region. Description: Body elongated, with round posterior and anterior ends. Ratio of the body width/length 1:7. Numerous scale-like spines present on the body tegument, in the anterior third of body. Oral sucker subterminal, rounded to oval, with several papillae on the buccal cavity. Ventral sucker rounded, smaller than oral sucker, preequatorial, and possesses a suctorial muscular disc bearing nine minute papillae around the disc. Oral sucker/ventral sucker ratio 1:0.58 in length and 1:0.58 in width. Mouth opens in the middle of oral sucker. Prepharynx conspicuous. Pharynx small, muscular, surrounded by medial glands that extend to the esophagus level. Oesophagus larger than oral sucker, thin. Caeca posteriorly to almost reach the end of body. Testes oval to rounded, in tandem, and are located at mid-level of body, mostly intercaecal and sometimes overlapping the caeca ventrally. Cirrus pouch well-developed, large, and contains a bi-partite seminal vesicle, prostatic gland and unarmed and coiled cirrus. Cirrus opens into the genital pore that is immediately preacetabular. Ovary located sinistrally to the ventral sucker, ovoid, smaller than testes. Seminal receptacle ovoid, located postero-dorsal to ovary. Mehli’s gland inconspicouos, covered by the seminal receptacle. Uterus coiled, and the uterine loops transversally arranged, occupying the posterior region of body. In midbody, uterine loops intercaecal with some overlapping the caeca. Muscular metraterm almost as large as the cirrus, opening into the genital pore. Vitelline gland follicular, which is distributed into two fields along the caeca, from the level of the seminal receptacle to the posterior border of the posterior testis. Posteriorly to testes, follicles are confluent dorsally. Eggs operculated, yellow, and measure 48–58 µm long by 18–26 µm wide. Excretory vesicle “I” shaped extending to the level of posterior testis. Excretory pore terminal. Host, geographic distribution and specimen deposition Bufo boreas: U.S.A.: Idaho (Waitz, 1959); Idaho, U.S.A., (Waitz, 1961); “ U.S.A. ” (Walton 1962). Rana luteiventris: U.S.A.: Glacier National Park, Montana. Specimen deposition: CNHE: 4692. Rana pretiosa: Canada: Postill Lake, Kelowna, British Columbia, Coleman, Alberta (Holmes pers. comm in O´ Grady, 1987). Manning Park, Okanagan Falls, Wilgress Lake, Champion Lakes, Creston and Loon Lake, British Columbia (O´ Grady, 1987); Trail, British Columbia (Rannala, 1990, 1991, 1992). U.S.A.: Bothell, Washington (Lucker, 1931); Springville, Utah (Olsen, 1937b); Idaho (Waitz, 1959, 1961, 1962); North West (Pratt & McCauley, 1961); Spokane County, Washington (Current & Lang, 1975); Pelican Creek, Wyoming (O´ Grady, 1987); Northern Idaho (Russell & Wallace, 1991). Specimen deposition: USNPC: 9025, 9026, 29903, 29904, 31021. Rana pipiens: U.S.A.: Lake and Flathead counties, Montana (Holmes pers. comm in O´ Grady, 1987). Rana pretiosa x Rana sylvatica: U.S.A.: Idaho (Waitz, 1959). Rana sylvatica: Canada: Gorge Creek, Alberta (Holmes com. per. in O´ Grady, 1987). Life cycle The life cycle of Glypthelmins intestinalis was elucidated by Olsen (1937b), Schell (1965), and Current & Lang (1975). Adults inhabit the intestine of Rana pretiosa, and the embrionated eggs are released to the environment with the feces and are ingested by snails (Physa spp., Helisoma spp.. and Lymnaea spp.). Once inside the intestine of the first intermediate host, eggs hatch and the miracidium is released penetrating the stomach epithelium. Miracidium is then transformed to mother sporocyst and then daughter sporocysts are formed within each mother sporocyst. Each daughter sporocyst produces lophocerc xiphicocercariae that are released from the snail as free-living forms. Cercariae penetrate the skin of frogs, lose the caudal region and transform into metacercariae that encyst in the frog’s epidermis. Metecercaria are ingested when adult frogs feed upon their skin during molt. GenBank 28S: AY875673 (1139 bp).
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 | 0,001 |
| Communication savante | 0,000 | 0,001 |
| Science ouverte | 0,000 | 0,001 |
| Intégrité de la recherche | 0,000 | 0,000 |
| Charge utile insuffisante (le modèle a refusé de juger) | 0,010 | 0,003 |
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 ».