Naineris chilensis Hartmann-Schroder 1965, New Status
Notice bibliographique
Résumé
Naineris chilensis Hartmann-Schröder, 1965, New Status Figures 46–47 Naineris dendritica chilensis Hartmann-Schröder, 1965: 195 –197, figs. 179–180; Rozbaczylo 1985: 130. Material examined. Ecuador, Anton Bruun Sta. 66-70 (1, USNM 60641), 8–9 m; 3 juveniles (USNM 60637).— Peru, South of Callao, Anton Bruun Sta. 65-215, shallow subtidal (USNM 60640).— Chile, Arica Province, Aricia, 18°29′33″S, 70°19′17″W, intertidal shale, coll. Eric Guiler, Papudo Corvette sta. N 17, 26–28 Feb 1955 (1, LACM- AHF Poly 5021); Chile, Puerto Aguirre, coll. 21 Jul 1958, 10 m, holotype of Naineris dendritica chilensis (ZMH- P-15326). Description. A large species, Chilean specimen [Holotype of N. dendritica chilensis] from Puerto Aguirre 60 mm long, 6 mm wide for approximately 250 setigerous segments. Body broad, depressed in thoracic region, cylindrical in abdominal region. Thorax with 15–30 setigers, depending upon size: larger specimens with more thoracic setigers. Branchiae from setiger 7–8, continuing to posterior end. Prostomium broadly rounded on anterior margin (Figs. 46 A, 47A); no eyespots; no nuchal organs observed. Peristomium a single narrow folded achaetous ring (Figs. 46 A, 47A); proboscis large, multilobed (Fig. 46 A). Thoracic notopodial postsetal lamellae broadly triangular (Fig. 46 B); abdominal notopodial postsetal lamellae similar, but not as broad and elongated (Fig. 46 C). Thoracic neuropodial postsetal lobes foliaceous ridges with uppermost edge prolonged (Fig. 46 B); abdominal neuropodial postsetal lobes lower, less foliaceous (Fig. 46 C). Thoracic notosetae all crenulated capillaries; abdominal notosetae including capillaries, 2–3 furcate setae and 5–6 deeply imbedded aciculae; furcate setae with unequal tynes, longest blunt on tip, shortest thin, pointed, with about 10 thin needles between tynes (Fig. 47 D); shaft with numerous crowded transverse rows of barbs merging with bases of needles. Thoracic neurosetae including three rows of uncini and subuluncini intermixed with capillaries (Fig. 47 B), especially in ventral-most portion of fascicles; uncini including smooth spines (Fig. 46 F) and less numerous smaller, weakly ribbed uncini (Fig. 46 D); subuluncini with minute barbs on capillary extension (Figs. 46 E, 47B). Abdominal neurosetae including capillaries and 5–6 smooth spines (Figs. 46 G, 47C). Abdominal parapodia dorsally elevated, forming channel with parapodia and setae of right and left sides nearly overlapping medially. Anus terminal, surrounded by lobes, cirri lacking. Remarks. N. dendritica chilensis Hartmann-Schröder is here raised to full species status. This species is similar to N. dendritica, but differs because the neuropodial postsetal lobes are prolonged on their superior most margins instead of being reduced to a small papilla as is typical for N. dendritica. Furthermore, the thoracic neuropodial uncini are mostly smooth instead of being mostly ribbed. The three juvenile specimens from Ecuador (USNM 60637) have more uncini with transverse ridges in the thoracic neuropodia than the adults, but an adult identification was confirmed for the same sample and it is not known how the various setal types develop in orbiniids. N. chilensis is also similar to N. laevigata Grube, 1855 originally described from the Mediterranean, but widely reported elsewhere in the Atlantic and Pacific Oceans. The branchial distribution reported for N. laevigata is highly variable and at odds with the majority of the genera and species examined as part of this study, where the branchiae of individual species have either a fixed segment on which they begin or at most only a narrow range of segments; exceptions are species where the branchiae begin in far posterior thoracic setigers. For N. laevigata, Eisig (1914) indicated most of the specimens he examined had branchiae from setigers 7–8, as in N. chilensis, but did range from setigers 4–11. Hartman (1957) referred North Pacific records of N. laevigata to N. dendritica, but retained the records of N. laevigata of Monro (1933b) from the Galápagos Islands and Ecuador and added additional specimens from Peru. For these collections, Hartman (1957) noted a wide range from setigers 6–12 as a starting point for the branchiae suggesting that more than one species might be present. Variability in other characters was not observed and apart from notes on records from Florida (branchiae from setiger 4) little comparative information was presented by Hartman (1957). However, the branchial distribution reported for N. laevigata from the Americas at a minimum, is so variable, that it is likely that several species are involved. A review of the widely distributed records of N. laevigata is clearly needed. Based on my own observations of N. dendritica from the eastern North Pacific (Blake 1996) and the few specimens of N. chilensis available for study, the differences between the two species are not great and they likely represent a sibling species pair with subtle parapodial and setal differences representing a clinal variation over the distribution from Canada to Chile. Distribution. Ecuador to Chile, intertidal to 10 m.
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 | 0,002 | 0,002 |
| Communication savante | 0,001 | 0,003 |
| Science ouverte | 0,001 | 0,002 |
| Intégrité de la recherche | 0,001 | 0,001 |
| Charge utile insuffisante (le modèle a refusé de juger) | 0,031 | 0,008 |
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 ».