Notice bibliographique
Résumé
Genus Eupronoe Claus, 1879 (Figs 5–6) Eupronoe Claus, 1879: 23 (key), 26–28.— Gerstaecker 1886: 484 –485.— Claus 1887: 48 (key), 50–52.— Stebbing 1888: 1509.— Chevreux & Fage 1925: 425.— Spandl 1927: 216 (key).— Pirlot 1929: 147.— Hurley 1955: 174 (key), 175.— Yoo 1971: 61 (key).— Bowman & Gruner 1973: 42 (key), 43.— Zeidler 1978: 21 (key), 21–22.— Vinogradov et al. 1982: 361 (key), 362.— Shih & Chen 1995: 146 (key), 148.— Vinogradov 1999: 1203 (incl. key). Type species. Eupronoe maculata Claus, 1879 by page priority. Type material could not be found at the MFN or ZMH and is considered lost. However, the description and figures provided by Claus (1879, 1887) readily characterise this genus. The type locality is the tropical south-west Indian Ocean, off Zanzibar. Diagnosis. Body shape robust or globular. Head round. Rostrum only present in males, short and rounded. Eyes occupying most of head surface; grouped in one field on each side of head. Antennae 1 of males with 3- articulate peduncle; flagellum with large, crescent-shaped callynophore, with aesthetascs arranged in one-field brush medially; with three smaller articles inserted on antero-dorsal corner. Antennae 1 of females with 3-articulate peduncle; flagellum with narrowly rectangular callynophore; with two smaller articles inserted terminally. Antennae 2 inserted on ventral surface of head in groove. Antennae 2 of males 5-articulate; strongly zig-zagged, with most articles folded back on each other; extending anteriorly under head and posteriorly into antennal pocket of gnathopod 1; basal article elongate, sub-equal in length to following article; terminal article very short, not folded, pointing posteriorly. Antenna 2 of females 5-articulate. Mandibular incisor relatively broad, with several teeth, with small distal lobe medially; in male orientated at right angles to palp. Maxillae 1 consisting of elongate, lobes, with four rounded teeth distally on medial margin. Maxillae 2 consisting of relatively broad lobes, pointed distally, with rounded medial bulge. Maxilliped with inner lobes completely fused; medial margin of outer lobes with fringe of closely packed slender setae. Gnathopod 1 sub-chelate; basis with antennal pocket in male, with fold of articles 2 & 3 of antennae held in pocket; carpal process rounded, armed with microscopic teeth or setae. Gnathopod 2 chelate; carpal process knife-shaped, armed with microscopic teeth or setae. Pereopods 3 & 4 distinctly shorter than pereopods 5 & 6. Pereopod 5; basis about 3 x as wide as merus; may overlap with P6 and lock proximally; articles 3–7 inserted terminally, or almost sub-terminally, to basis. Pereopod 6; basis very broad, more than 5 x as wide as merus, but not operculate; articles 3–7 inserted sub-terminally on basis; merus with antero-distal corner extended, distinctly overlapping carpus medially. Pereopod 7 reduced in size with large basis, with only 1–3 terminal articles. Uropoda all with articulated exopoda and endopoda. Uropod 2; endopod and exopod leaf-like, foliaceous with smooth margins. Uropod 3; endopod, and sometimes also exopod, leaf-like, foliaceous, with smooth margins. Species. Eupronoe maculata Claus, 1879; E. armata Claus, 1879; E. minuta Claus, 1879; E. intermedia Stebbing, 1888 and E. laticarpa Stephensen, 1925. Sexual dimorphism. Apart from the morphology of the mandibles, the antennae, and the antennal pocket of gnathopod 1, males differ from females in having a slightly more pointed head, the carpus of gnathopod 1 is generally broader, and the carpal process of gnathopod 2 ends in a sharper point. Females also tend to have a more robust pereon. Remarks. In all species, the coxa of pereopod 5 articulates proximally with the coxa/basis of pereopod 6, as in Parapronoe. Similarly all species have a weak, ridge/groove locking mechanism near the proximal, anterior corner of the ischium of pereopods 5 & 6, and pleonites 1–3 have a slight lateral ridge, that lines up with the posterior margin of pereopod 6, when the animal is curled. Also, like Parapronoe, the cuticular sculpture is relatively prominent, consisting of circular markings or pits, or dorso-ventral striations; characters which can be used to help distinguish species. Virtually nothing is known about the biology of species, but they seem to be associated with salps, or siphonophores, or both. Eupronoe maculata has been recorded with salps (Spandl 1927), and E. minuta has been found associated with the siphonophores, Agalma elegans (Harbison et al. 1977), Apolemia uvaria, and Sulculeolaria quadrivalvis (Laval 1980) and Rosacea cymbiformis (Gasca et al. 2014), and has also been found with the salp Thalia democratica (Young & Anderson 1987—misidentified as E. armata). Eupronoe is widely distributed in tropical and warm-temperate regions of the world’s oceans and can, at times, be relatively abundant in plankton hauls near the surface (Stephensen 1925, Pirlot 1939). Species of Eupronoe are particularly difficult to determine with certainty because of the sexual dimorphism, morphological changes due to growth, and moulting, and the lack of adequate illustrations in the literature. Zeidler (1992 a, 1998) gives more information on all species, together with some illustrations. Vinogradov et al. (1982) recognise four species; to this should be added E. intermedia Stebbing, 1888, which Tashiro (1978) demonstrated to be a valid species, distinguished from E. armata Claus, 1879.
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 | 0,001 |
| 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 | 0,000 |
| 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) | 0,021 | 0,006 |
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 ».