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Enregistrement W6950250948 · doi:10.5281/zenodo.6093737

Sertularella pacifica Choong, 2015, sp. nov.

2015· article· en· W6950250948 sur OpenAlexaboutno aff

Notice bibliographique

RevueZenodo (CERN European Organization for Nuclear Research) · 2015
Typearticle
Langueen
DomaineMaterials Science
ThématiqueDiatoms and Algae Research
Établissements canadiensnon disponible
Organismes subventionnairesnon disponible
Mots-clésQueen (butterfly)StolonPlant stemApex (geometry)Land area

Résumé

récupéré en direct d'OpenAlex

Sertularella pacifica sp. nov. (Figure 6) Sertularella fusiformis — Torrey, 1902: 61, pl. 6, fig. 53–54.— Fraser, 1937: 153, pl. 34, fig. 181 [not Sertularella fusiformis (Hincks, 1861)] Material. Holotype: CANADA: British Columbia. Vancouver Island, Juan de Fuca Strait, Race Rocks, 48˚18’00”N, 123˚32’00”W, 0 5. iv.1986, 6–10 meters, two short hydrocauli, with gonothecae, coll. A. Brinckmann- Voss, ROMIZ B670. Paratype: CANADA: British Columbia. Queen Charlotte Land District. Masset Harbor, 14. ix.1935, without gonothecae, ROMIZ B4065. Other material: CANADA: British Columbia. Queen Charlotte Land District. Masset Harbor, 54˚03’00”N, 132˚13’00”W, 14. ix.1935, colony arising from stolon at the base of Abietinaria pulchra (Nutting, 1904) colony, without gonothecae, ROMIZ B4066. CANADA: British Columbia. Queen Charlotte Land District. Masset Harbor, 14. ix.1935, two short hydrocauli, without gonothecae, ROMIZ B4067. CANADA: British Columbia. Queen Charlotte Land District. Masset Harbor, 14. ix.1935, colony arising from stolon at the base of Sertularia sp.colony, without gonothecae, ROMIZ B4068. CANADA: British Columbia. Queen Charlotte Land District. Masset Harbor, 54˚03’00”N, 132˚13’00”W, 14. ix.1935, hydrocauli, without gonothecae, ROMIZ B4069. Reported distribution. California: San Francisco, as Sertularella fusiformis (Hincks, 1861) (Torrey, 1902). Oregon: Three locations off Heceta Head, 0–113 meters (Fraser, 1937). Description. Colonies erect, hydrorhiza stolonal, occasionally anastomosing. Hydrocaulus geniculate, unbranched. Perisarc thickened throughout, up to 60 mm thick. Hydrocaulus monosiphonic, unfascicled, divided into internodes. Internodes 1003–1530 mm long, with one to three (usually two) complete annulations basally; proximal-most annulation often spirally twisted (Fig. 3 A,B). Internode has tendency to spiral relative to main axis. Single hydrotheca distal to internode. Hydrothecae alternate, often not on same plane (Fig. 3 A). Hydrotheca tubular, walls asymmetrical; abcauline and adcauline wall slightly swollen basally, swelling on abcauline wall more proximal. Perisarc of hydrothecae thickened, up to 60 mm thick. Distal half of hydrotheca narrowed towards aperture, greater narrowing on abcauline side. Adcauline hydrothecal wall adnate for approximately 1/4–1/2 of length. Hydrothecal margin dentate with four equally-developed cusps; one adcauline, one abcauline, and two laterals. Opercular flaps triangular, four present; when closed forms roof extending slightly beyond opercular margin. Intrathecal cusps present, three in number, occasionally missing; two small intrathecal cusps proximal to and flanking adcauline marginal cusp, one long and narrow intrathecal cusp on abcauline side (Fig 3 A). Gonothecae (♂) few, attached to internode or directly below base of hydrotheca; large, up to three-times longer than hydrothecae, spindle-shaped, widest medially, longer than wide, flexed or bent mid-axis. Gonothecal body strongly annulated throughout; 10–12 complete, well-developed annulations. Neck short or barely discernible, four low rounded cusps around gonothecal aperture. Occasionally, one of the four cusps may be more developed than other three. Differential diagnosis. The records from the west coast of North America (Torrey 1902; Fraser 1937) seem to be morphologically distinct from descriptions of S. fusiformis elsewhere as shown by the absence of four intrathecal cusps and the presence of two annulations at the base of the internodes. These descriptions correspond to the specimens examined by the author in this study. Given the variability of the species included in the S. fusiformis / S.ellisii complex, this species was most likely misidentified as S. fusiformis. Measurements of the internodes, hydrothecae, and gonothecae (Table 4) show that these specimens are much larger than S. fusiformis. The intrathecal cusps are never as well-developed as in S. fusiformis. Moreover, the hydrothecae of Sertularella pacifica sp. nov. lack the considerably swollen basal portion and strongly tapered upper portion characteristic of the fusiform hydrothecal shape, and the gonothecae are distinct from those belonging to S. fusiformis in being spindle-shaped and bent around their mid-axis. Remarks. This material agrees with the hydroids attributed to Sertularella fusiformis (Hincks, 1861) from the west coast of North America by Torrey (1902), and subsequently included in reports by Fraser (1911, 1937). Sertularella fusiformis is well distributed in temperate and subtropical parts of the Atlantic as well as in the Mediterranean, but records of occurrences elsewhere are few and dispersed (Ramil et al. 1992). The latter are from the Indian Ocean coast of South Africa (Millard 1975) and from the Pacific coast of North America: Californian Pacific coast (Fraser 1911); off Heceta Head, Oregon (Fraser 1937). I consider the reports of Sertularella fusiformis from the Pacific coast of North America to be erroneous. Its biogeographic distribution, and the distinct morphological characteristics of Sertularella pacifica set this species apart from its congeners. Even within the Atlantic, it is probable that the nominal species Sertularella fusiformis is part of a species complex. Sertularella fusiformis, along with S. mediterranea, S. ellisii, S. ornata, and S. polyzonias are morphologically similar and so have been variously kept separate or synonymised with other taxa (Cornelius 1979; Ramil et al. 1992; Medel & Vervoort 1998). Millard (1958) considered S. fusiformis to be a variable species, but accepted the diagnostic value of the presence of 4 intrathecal cusps that alternate with the marginal cusps in this species, a view shared by Corrales et al. (1980). Others, such as Picard (1956) considered S. fusiformis to be an extreme, Atlantic form of S. ellisii. 16S genetic data has provided evidence that nominal species of Sertularella fusiformis from Madeira and the Azores in the North Atlantic fall into distinct clades likely corresponding to different species (Moura et al. 2011). Etymology. The species name refers to the Pacific Ocean and emphasizes its distinctiveness from its congeners elsewhere.

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 enseignants

Ni 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.

score de la tête « metaresearch » (Codex)0,000
score de la tête « metaresearch » (Gemma)0,001
Version: metacan-v3-hybrid-931329e0061cStatut de validation: machine_predicted_unvalidated
Catégories candidatesaucune
Catégories consensuellesaucune
DomaineSignal candidat: aucune · Signal consensuel: aucune
Devis d'étudeSignal candidat: Sans objet · Signal consensuel: aucune
GenreSignal candidat: Empirique · Signal consensuel: aucune
Score de désaccord entre enseignants0,053
Score d'incertitude au seuil0,106

Scores du classifieur distillé par catégorie (deux têtes)

CatégorieCodexGemma
Métarecherche0,0000,001
Méta-épidémiologie (sens strict)0,0010,001
Méta-épidémiologie (sens large)0,0010,000
Bibliométrie0,0020,003
Études des sciences et des technologies0,0030,001
Communication savante0,0010,003
Science ouverte0,0010,002
Intégrité de la recherche0,0010,001
Charge utile insuffisante (le modèle a refusé de juger)0,0100,005

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.

Tête enseignante Opus0,055
Tête enseignante GPT0,276
Écart entre enseignants0,221 · la distance entre les deux têtes enseignantes sur ce seul travail
Statut de validationscore_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 découle

Classification

machine, non validée

Prédiction automatique; un appel candidat d’une seule source (Gemma direct ou Codex distillé), pas un consensus.

Les modèles n’ont appliqué aucune catégorie : rien dans la taxonomie ne correspondait à ce travail.
Devis d'étudeSans objet
Domainenon disponible
GenreEmpirique

Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».

En bref

Citations0
Publié2015
Routes d'admission1
Résumé présentoui

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