Paranoplocephala primordialis Douthitt 1915
Notice bibliographique
Résumé
Paranoplocephala primordialis (Douthitt, 1915) (Fig. 2, Table 2) Syn. Andrya primordialis Douthitt, 1915. Redescription: Based on three specimens from T. hudsonicus (Tables 1 and 2). For the early uterus and other illustrations of the type material, see Douthitt (1915). Fully gravid strobila ca. 85 long (n=1) and 2.0 (n=1) wide (1.0 in Douthitt 1915). Number of proglottids ca. 300 (n=1). Proglottids craspedote, but velum very short or absent in well-relaxed specimens. Length/width ratio of mature proglottids 0.21–0.44 (0.33, n=6), of gravid proglottids 0.38–0.62 (0.46, n=5). Scolex simple, globular, rounded apically; width 0.46–0.53 (n=2) (0.475 in Douthitt 1915). Suckers 0.175–0.220 (0.20, n=8) in diameter, directed antero-laterally, embedded in scolex. Neck 0.5 (n=1) long, not clearly distinct from scolex, tapering posteriorly, minimum width (0.15–0.26, n=2) attained in region where segmentation first visible. Genital pores unilateral (n=1) or with multiple (18) alternations per strobila (n=1), opening slightly posterior to middle of proglottid margin in mature proglottids. Ventral longitudinal osmoregulatory canals of variable width (0.04–0.10, 0.058, n=7). Dorsal longitudinal osmoregulatory canals lateral to ventral longitudinal canals. Genital ducts passing dorsally to longitudinal osmoregulatory canals. Number of testes 22–40 (30.2, n=9) (30–40 in Douthitt 1915), distributed in single group antiporally and anteriorly to ovary. Poral testes reach level of poral margin of vitellarium or ovary, or poral longitudinal ventral canal (but not overlapping latter). No testes found lateral to antiporal longitudinal ventral canal (n=9). Testes overlap anterior and antiporal margins of ovary, being in contact with antiporal lobe of vitellarium in one specimen. Diameter of testes variable (0.035–0.110). Cirrus sac 0.12–0.20 (0.16, n=7) long in mature proglottids or 19–26% (n=3) of proglottid width, overlapping or extending across longitudinal ventral canal. Maximum length of cirrus sac in postmature proglottids 0.19–0.22 (n=3). Muscle layers of cirrus sac thin. Ductus cirri armed densely with minute spines in its distal part. Internal seminal vesicle occupying up to half of cirrus sac length when filled with sperm. External seminal vesicle slightly pedunculated, distinctly set off from vas deferens, covered by large, poorly-stained cells. Ovary coarsely lobed, 0.15–0.34 (0.24, n=6) wide or 33–39% (n=3) of proglottid width, positioned medially or slightly antiporally, not filling whole space between ventral longitudinal canals. Vitellarium asymmetrically bilobed or irregularly shaped, positioned medially or slightly porally with respect to midline of ovary and proglottid (index of asymmetry 0.46–0.49, n=3), overlapping markedly posterior part of ovary. Vagina 0.13–0.17 (0.15, n=7) long, usually somewhat shorter than cirrus sac (75–100%, n=3), slightly curved, running posteriorly or postero-ventrally to cirrus sac, set off from seminal receptacle by slight constriction. Internally, vagina formed by tube with distinct wall; vaginal lumen wide. Internal surface of vagina lined at least proximally with delicate hairs pointing distally (seen poorly in whole-mounts). Vaginal tube and internal surface of poral region of seminal receptacle covered by layer of large cells. Seminal receptacle 0.09–0.15 (0.11, n=7) in diameter in mature proglottids, spherical or subspherical, even before being filled with sperm. Seminal receptacle retains its shape in postmature proglottids, attaining diameter of 0.15–0.18 (n=3). Early uterus not seen in whole-mounts; in sectioned type material it appears as loose network of anastomosing tubes in anterior part of mature proglottids. Uterus in pregravid proglottids filling most of medulla with few large anterior, posterior and lateral sacculations or diverticula and relatively simple system of internal trabeculae. Genital ducts, sacculations and trabeculae disappear in fully gravid proglottids. Eggs 0.060–0.070 (0.066, n=5) long, spherical in surface view, ovoid in side view. Pyriform apparatus present. FIGURE. 2. Paranoplocephala primordialis from Tamiasciurus hudsonicus. A. scolex (Wyoming). B. Mature proglottid (Minnesota, reconstruction of sectioned type material; redrawn from Haukisalmi & Henttonen 2001. C. Terminal genital ducts (Minnesota, sectioned type material). D. Mature proglottid (Quebec). E. Pregravid uterus (Minnesota, sectioned type material). Scale-bars in mm. Remarks. Paranoplocephala primordialis was described from the red squirrel T. hudsonicus from Minnesota, U.S.A. (Douthitt 1915), and it has later been reported from Microtus and Myodes voles in various parts of North America (Table 1). However, we suggest that P. primordialis is a host-specific parasite of T. hudsonicus, because it is morphologically distinct from the P. primordialis -like species in voles (see below). In addition to the type region (Minnesota), P. primordialis has been found in T. hudsonicus from Wyoming (U.S.A.), Alberta, Saskatchewan and Quebec (Canada) (Table 1). However, P. primordialis was not found during an examination of ca. 50 red squirrels and 100 Arctic ground squirrels (Spermophilus parryii) in various parts of Alaska (unpublished BCP data). Also, P. primordialis -like cestodes were not found in the red squirrel or other sciurids in the North Central States of the U.S.A. (Ohio, Michigan, Illinois, Wisconsin, Minnesota; Rausch & Tiner 1948), or in the red squirrel or Abert's squirrel (Sciurus aberti) in New Mexico (Patrick & Wilson 1995).
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 | 0,000 |
| 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 | 0,000 | 0,000 |
| Charge utile insuffisante (le modèle a refusé de juger) | 0,006 | 0,002 |
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 ».