Arostrilepis cooki Makarikov, Galbreath & Hoberg, 2013, sp. n.
Notice bibliographique
Résumé
Arostrilepis cooki sp. n. (Figs. 4, 5) Type host: Myodes gapperi (Vigors) (Rodentia: Cricetidae: Arvicolinae). Other hosts: Currently unknown. Type locality: Near Meziadin Junction, British Columbia, Canada (56o21’55”N, 129o16’28”W). Other localities: Taft Creek, British Columbia (56o29’46”N, 129o25’31”W); near Bell II, British Columbia, south side Deltaic Creek (ca., 56o32’38”N, 129o32’39”W); Pattee Canyon, Missoula Co., Montana, USA (46o48’N, 113o57’W). Type material: Holotype MSB Para 1244 (field number IF 6750/ cyt- b sequence) from type host and locality by A.M. Runck et al., 9 June 2003. Paratypes from type host species: MSB 1245 (IF 6751/ cyt- b sequence) by A.M. Runck et al., at type locality, 9 June 2003; MSB 1249–1252 (IF 6830 C2; 6830 C3; 6830 C4; 6830 C6/ cyt- b sequence) by A.M. Runck et al., at Taft Creek, British Columbia, 14 June 2003; MSB 1217 (JMK 02-10), collected by J. M. Kinsella at Pattee Canyon, Montana, 10 October 2002; MSB 1246–1248 (IF 6827 C1; 6827 C2; 6827 C3) by A. Runck et al., at Bell II, British Columbia, 14 June 2003. Symbiotype: Myodes gapperi (IF 6750) at type locality, skull and skeleton in MSB Mammalogy Division. Description: Based on 8 specimens. Fully developed strobila up to 150 mm long, with maximum width at postmature or pregravid gravid proglottides, 1.25–1.4 mm. Strobila flat, consisting of about 850 craspedote proglottides. Scolex slightly compressed dorso-ventrally, 280–372 (324, n = 4) wide, clearly wider than neck. Suckers unarmed, ovoid in surface view, 162–238 × 124–195 (190 × 161, n = 8), with thin walls, prominent (Fig. 4 A, B). Rhynchus and rostellar apparatus absent. Neck relatively long and narrow, 160–200 (178, n = 8) wide. Two pairs of osmoregulatory canals, without transverse anastomoses. Dorsal osmoregulatory canals thin, 0.5–2 (1.2, n = 10) wide, situated predominantly in same sagittal plane as ventral canals. Ventral osmoregulatory canals 30–65 (44, n = 15) wide. Position of dorsal osmoregulatory canals not always constant; loops may be situated laterally to ventral canals. Genital pores unilateral, dextral. Genital ducts usually pass dorsally to longitudinal osmoregulatory canals, position of genital ducts between osmoregulatory canals within single strobila appears rarely (Fig. 4 C, D). Development of proglottides gradual, protandrous. Strobilar part containing juvenile proglottides without external segmentation; proglottides become externally distinct at level of premature part of strobila. Mature proglottides 120–275 × 680–1040 (198 × 785, n = 12), transversely elongate, trapeziform (Fig. 4 C, D). Testes relatively large, usually three in number, almost of equal size, 115–175 × 85–125 (135 × 96, n = 25), round or oval, commonly situated in triangle; poral testis separated from two antiporal testes by female gonads. Arrangement of testes may vary (from triangle with flat angle to linear). Cirrus-sac relatively short, 190–218 × 35–48 (205 × 42, n = 15), with well-developed external muscular layers, commonly extends across ventral longitudinal canal (Figs. 4 D, 5C). Genital atrium simple, infundibular, deep, opens laterally about middle or slightly anterior of lateral proglottis margin. Cirrus 88–109 (98, n = 16) long, conical, with relatively wide basal region, 19–24 (21, n = 16) in diameter, and narrow distal region, 8–14 (11, n = 16) in diameter; armed along entire length with relatively large (up to 3.3–4 long) rosethorn-shaped spines (Fig. 5 A). Internal seminal vesicle with circular musculature, ovoid, 85–120 × 28–40 (95 × 33, n = 15), shorter than half of cirrus-sac length (Figs. 4 D, 5C). External seminal vesicle transversely elongate, 117–171 × 65–103 (151 × 78, n = 15), clearly outlined from vas deferens, slightly larger than seminal receptacle. Ovary 305–410 (329, n = 20) wide, median, fan-shaped, irregularly lobed, ventral to male genital organs, occupying substantial part of median field, slightly overlapping testes (Fig. 4 D). Vitellarium 60–117 × 115–172 (91 × 153, n = 20), postovarian, median, scarcely lobed. Vagina tubular, clearly distinct from seminal receptacle; ventral to cirrus-sac. Distal part of vagina 92–111 × 9–19 (100 × 13, n = 10), thick-walled, covered externally by dense layer of intensely stained cells; proximal part of vagina infundibular (Fig. 5 C). Conductive part of vagina 110–132 × 10–27 (122 × 17, n = 10), thin-walled, vastly varying in diameter depending on degree of distention with sperm. Seminal receptacle relatively small, transversely elongate, 80–122 × 40–77 (100 × 51, n = 14). Uterus appears as complex of fine-walled anastomosing tubes of varying length and diameter, positioned ventrally to other organs. With development of proglottides, tubular structures increase in width and uterus becomes labyrinthine. Testes remain in postmature and pregravid proglottides; cirrus-sac and vagina persist in gravid proglottides. Gravid proglottides transversely elongate, 185–360 × 810–1330 (261 × 1107, n = 10). Fully developed uterus labyrinthine, occupying entire median field, extending bilaterally beyond longitudinal osmoregulatory canals (Fig. 5 D). Uterus contains numerous (up to 1100) eggs. Eggs 31–38 × 58–72, elliptic, with thin outer coat (Fig. 5 B); oncosphere 13–17 × 18–23. Embryophore fusiform, 17–20 × 40–48, with straight polar processes. Embryonic hooks small, 7.5–8.3 long. Etymology: This species has been named in honor of Joseph A. Cook in recognition of contributions in understanding rodent systematics and biogeography, and innovative explorations of host-parasite associations among arvicoline rodents. Remarks: Arostrilepis cooki sp. n. is distinguished from congeners by the length and shape of the cirrus (Table 2). In specimens of A. cooki the cirrus is longer in comparison to A. beringiensis, A. microtis, A. tenuicirrosa, A. gulyaevi, A. mariettavogeae and A. schilleri. The cirrus is armed with relatively large rosethornshaped spines and has a conical form; these features distinguish A. cooki from A. beringiensis, A. intermedia, A. janickii and A. schilleri, which have cylindrical cirri, and from A. microtis, A. tenuicirrosa and A. gulyaevi, in which the cirri have a conical basal region and cylindrical distal region. Compared to A. cooki, the cirrus of A. tenuicirrosa is armed with relatively small needle-shaped spines. The form and the length of the cirrus of A. cooki are most similar to those of A. macrocirrosa, but in specimens of the former the cirrus is narrower in the basal region (Figs. 11, 12). Arostrilepis cooki is characterized by a relatively narrow strobila. The cirrus-sac is shorter than that in A. horrida and A. microtis but larger than in A. beringiensis, A. janickii, A. mariettavogeae and A. schilleri. The ovary is narrower relative to those in A. horrida, A. microtis and A. gulyaevi. The scolex and the suckers are larger in comparison to A. janickii. The egg and oncosphere are large relative to those in A. horrida, A. microtis and A. janickii (see Table 2). The proximal end of the cirrus-sac in hermaphroditic mature proglottides overlaps the ventral longitudinal osmoregulatory canal. This species can be distinguished from A. beringiensis as its testes are arranged in a triangle; in the latter species, the testes form a flat angle or are situated in one row. Similarly, the testes form one row in A. microtis and A. mariettavogeae. Furthermore, the external seminal vesicle is larger than the seminal receptacle, the gravid proglottides are transversely elongate, and the polar processes of the embryophore are straight in A. cooki. This species is a specific parasite of red-backed voles (Myodes) from North America.
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) | 0,001 | 0,000 |
| Méta-épidémiologie (sens large) | 0,000 | 0,000 |
| Bibliométrie | 0,002 | 0,001 |
| Études des sciences et des technologies | 0,001 | 0,001 |
| Communication savante | 0,000 | 0,001 |
| Science ouverte | 0,001 | 0,001 |
| Intégrité de la recherche | 0,001 | 0,001 |
| Charge utile insuffisante (le modèle a refusé de juger) | 0,011 | 0,005 |
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 ».