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Enregistrement W6931289597 · doi:10.5281/zenodo.6273193

Proceraea prismatica O.F. Muller 1776

2004· article· de· W6931289597 sur OpenAlexaboutno aff

Notice bibliographique

RevueZenodo (CERN European Organization for Nuclear Research) · 2004
Typearticle
Languede
DomaineAgricultural and Biological Sciences
ThématiqueMediterranean and Iberian flora and fauna
Établissements canadiensnon disponible
Organismes subventionnairesnon disponible
Mots-clésHolotypeGenBankSequence (biology)Taxonomy (biology)Type (biology)

Résumé

récupéré en direct d'OpenAlex

Proceraea prismatica (O.F. Müller, 1776) (Fig. 26A–E) Nereis prismatica O.F. Müller, 1776: 218; Fabricius 1780: 302 –303.? Nereis bifrons O.F. Müller, 1776: 218; Fabricius 1780: 303 –304. Amytis prismatica Savigny 1822: 46; Grube 1850: 311; Quatrefages 1866: 77. Nereisyllis prismatica Blainville 1828: 473. Polybostrichus longosetosus Örsted, 1843: 31 –32, figs 62, 67, 71. Polybostrychus longisetosus Grube 1850: 311. Polybostrichus longosetus Quatrefages 1866: 72. Autolytus incertus Malmgren, 1867: 35 –36, plate 6, fig. 40A–E. Proceraea gracilis Verrill, 1874a: 132; 1874b: 361, pl. 3, fig. 2; Webster & Benedict 1887: 723 – 724; Treadwell 1948: 30. Autolytus prismaticus Chamberlin 1920: 12 B; Berkeley 1923: 209 –210; Wesenberg­Lund 1947: 24 –30, figs 10–12; 1950: 50–51, fig. 13D; 1953: 38–39; Chlebovitch 1962: 169 –171, fig. 2; Pettibone 1954: 249 –252, fig. 29A–B; 1963: 139–141, fig. 37D; Imajima 1963: 352, pl. 12, fig. 12; Imajima & Hartman 1964: 99 –100, fig. 21A–G. Autolytus aurantiacus Berkeley & Berkeley 1938: 48. Autolytus trilineatus Berkeley and Berkeley, 1945: 318 –320, fig. 1A–B; 1948: 69–70, fig. 100; Pettibone 1967: 5. Proceraea prismatica Hamond 1967: 1 –4,fig. 3A–C; Hartmann­Schröder 1971: 184 –186, fig. 59E– I; Hamond 1972: 344; 1974; Kirkegaard 1992: 257 –259, fig. 127A–E; Hartmann­Schröder 1996: 190 –191, fig. 82A–E; Nygren & Sundberg 2003: GenBank sequences, 16S rDNA partial sequence AF474265, and 18S rDNA partial sequence AF474311. Autolytus (Proceraea) trilineatus Banse 1972: 197 –198, fig. 3A–C. Not Autolytus prismaticus Thorson 1946: 39 –40 (= Proceraea cornuta) Material examined. Norway: holotype of Autolytus incertus SMNH 2439, Spitsbergen, Whalers point, 77°35'N 20°5'E, Aug 1864. USA: holotype of Proceraea gracilis YPM 24230, Jul 1874; holotype of Autolytus trilineatus USNM 32881, New Castle Island, Nanaimo, British Columbia, 18 Jun 1943. Iceland: 4 spms, Breidafjördur, 65°N 23°W, dredge, 50 m, 15 Jul 1991; 1 spm in author's collection for DNA analyses, 64°15.5'N 22°01.7'W, dredge, 40 m, 26 Jun 1999. Faroes: 1 spm (rear end in author's collection for DNA analyses), South of Vagar, 61°56.8'N 6°59.5'W, triangle­dregde, 76–78 m, bedrock, gravel, hydroids, 27 Jun 1997; 1 spm (rear end in author's collection for DNA analyses), East of Bordøy, 62°04.2'N 6°33.8'W, triangle dredge, 57–58 m, shellgravel, 4 Jul 1997. Diagnosis. Proceraea with 3 longitudinal black lines. Description. Length 12.5–17 mm for 57–75 chaetigers, width 0.4–0.55 mm. Live specimens white, with 3 longitudinal black lines along most of body; one line at each side of body and one middorsal; eyes dark red. Lines fades in preserved material, but are sometimes retained. Ciliation present on prostomium, nuchal epaulettes, and a few segments ventrally. Eyes confluent (Fig. 26A, B); eye spots present (Fig. 26B). Palps in dorsal view projecting 1/4–1/3 of prostomial length, fused. Extension of nuchal epaulettes to beginning of chaetiger 1 (Fig. 26A). Median antenna reaching chaetiger 12–14 (n=2). Lateral antennae and dorsal tentacular cirri, length 1/2 of median antenna. Ventral tentacular cirri 1/2 as long as dorsal pair. First dorsal cirri as long as or 2/3 of median antenna, second dorsal cirri as long as tentacular cirri. From chaetiger 1–27 cirri with usual alternation in direction, followed by 4 DDUU­groups, and 3–4 DDU­groups (n=2). Dorsal cirri from chaetiger 3, of equal length, 2/3 or equal to body width. Cirrophores on tentacular segment and first dorsal cirri present; cirrophores otherwise absent. All appendages cylindrical. Parapodial lobes rounded conical, small. Anterior chaetigers with 2–3 aciculae, 1 in median and posterior. Chaetal fascicle with 10–13 compounds in anterior chaetigers, 5–10 in median and posterior. Compound chaetae with small distal tooth (Fig. 26D) in anterior chaetigers, more posterior with larger terminal tooth, still somewhat smaller than subdistal tooth; serration present. Single thick bayonet chaetae (Fig. 26E), beginning between chaetiger 7–25 (n=4). Pharynx with 1 sinuation anterior and lateral to anterior half of proventricle (Fig. 26B). Trepan in chaetiger 1–2, with 18 unequal teeth, 9 large and 9 smaller (Fig. 26C); 1 large alternating with 1 small, arranged in 2 rings. Basal ring present; infradental spines absent (Fig. 26C). Proventricle equal in length to 2.5 segments in chaetiger 6–9 (Fig. 26B) with 31–32 rows of muscle cells (n=4). Anal cirri equal in length to body width at level of proventricle. Reproduction. Schizogamy by anterior scissiparity. Two specimens with developing stolons behind chaetiger 13. Stolons found from February to December (Malmgren 1867; Chamberlin 1920; Berkeley 1923; Wesenberg­Lund 1947; Pettibone 1963; Hamond 1974). Morphology of epitokous stages. Male. No mature stolons examined. Örsted (1843), Wesenberg­Lund (1947), Pettibone (1963), and Hamond (1967; 1974) provide information on stolon morphology. Length c. 10 mm for 6+(23–35)+(21–30) chaetigers (Wesenberg­Lund 1947; Pettibone 1963). Information on colour pattern lacking. Median antenna reaching chaetiger 9–14 (Wesenberg­Lund 1947; Hamond 1967). Lateral bifid antennae, basal part 1/2 of total length, its rami of about equal length. Frontal processes present. Tentacular cirri 2 pairs (Wesenberg­Lund 1947). First dorsal cirri, longer than median antenna (Wesenberg­Lund 1947); achaetous knobs present (Hamond 1974). Cirri in region a reciprocally equal, slightly longer than cirri in region b, cirri in region c much shorter (Wesenberg­Lund 1947: fig. 12). Cirri in region a fusiform (Örsted 1843: fig. 62; Wesenberg­Lund 1947: fig. 12), cirri in region b cylindrical. Female. Based on holotype of Autolytus incertus. Length 8 mm for 6+19+24 chaetigers width in region a 0.4 mm, width in region b 0.8 mm. Pettibone (1954) gives these measurements: 9 mm for 6+18+34 chaetigers. Preserved material without colour markings, live specimens with same colour pattern as in atokes (Pettibone 1954). Ciliation not assessed. Prostomium with straight anterior margin. Nuchal epaulettes triangular, reaching half of chaetiger 1. Median antenna reaching chaetiger 4–5. Lateral antennae and first pair of dorsal cirri, equal in length to median antenna. Tentacular cirri 2 pairs, dorsal pair 2/ 3 in length of median antenna, ventral pair 1/ 3 in length of dorsal pair. First dorsal cirri, equal in length to dorsal tentacular cirri; achaetous knobs present. Cirri in region a, equal to body width; cirri in region b longer than in region a, equal to body width; cirri in region c successively shorter towards the end, c. 1/3 of body width. Small indistinct tentacular cirrophores, cirrophores on all dorsal cirri, except in posterior part of region c, present. All appendages cylindrical. Region a and b with 2 neuropodial aciculae; 3 anterodorsal, and 6–7 posteroventral notopodial aciculae in region b. Neuropodial chaetal fascicle with c. 10 compound chaetae. Notopodial chaetal fascicle with c. 20 swimming chaetae. Anal cirri lost. Habitat. Hydroids, gravel, sublittoral. Distribution. North Atlantic, North Pacific, Arctic. Remarks. Proceraea prismatica is unique in having 3 black lines, other Proceraea with longitudinal lines have either 2 or 4 lines. Preserved specimens might be difficult to separate from similar taxa with the same length in nuchal epaulettes. Molecular data suggests that its closest relative is Proceraea hanssoni n. sp. (Nygren & Sundberg 2003). The suggested synonomy of Polybostrichus longosetosus is concluded from literature, synonymy of Autolytus incertus, Proceraea gracilis, and A. trilineatus is based on examination of type material. Proceraea rubroproventriculata Nygren & Gidholm, 2001 (Fig. 27A–E) Proceraea rubroproventriculata Nygren & Gidholm, 2001: 184 –187, figs 2D–E, 5A–E, 6A–D, 7; Nygren & Sundberg 2003: GenBank sequences, 16S rDNA partial sequence AF474276, and 18S rDNA partial sequence AF474322. Material examined. USA: holotype (LACM­POLY 1964), 1 paratype (LACM­AHF POLY 1965), and additional 4 spms (2 mounted for SEM), Florida, Key Biscayne, Crandon marina, 25°43.4'N, 80°10.4'W, orange sponge, 0.5 m, 11 Mars 1971; 1 spm, Florida, Biscayne bay, 25°31–34’N, 80°12.3'W, Porites and small sponges Haliclona viridis, 1 m, 22 Feb 1971. Brazil: 1 spm mounted for SEM, 4 spms on slides, 4 spms in author's collection for DNA analyses and 1 additional spm, Baía de Paranaguá, west Ihla do Mel, 25°34.55'S, 48°19.19'W, dive, 10 m, boulders with epifaunal mat, 15 Aug 1998. Diagnosis. Proceraea with anterior and posterior third of proventricle orange­red, and with 12+12 teeth in trepan. Description. Length 4.2–10.7 mm for 35–53 chaetigers, width 0.2–0.25 mm. Live specimens without colour markings, transparent to weakly brownish or orange­red in anterior part, especially laterally; anterior and posterior part of proventricle red (Fig. 27A); parapodial bases in Brazilian specimens with 3 or 4 red spots in a transverse row; eyes red. Preserved material without colours. Ciliation present on prostomium, nuchal epaulettes, and a few segments ventrally. Eyes confluent (Fig. 27A); eye spots present. Palps in dorsal view projecting 1/3–1/2 of prostomial length (Fig. 27A), fused. Nuchal epaulettes extending over tentacular segment (Fig. 27A). Median antenna reaching chaetiger 13–16 (n=4). Lateral antennae and dorsal tentacular cirri, length 1/2–2/3 of median antenna. Ventral tentacular cirri 1/2 as long as dorsal pair. First dorsal cirri as long as median antenna, second dorsal cirri as long as ventral tentacular cirri. Alternation in direction of cirri not assessed. Dorsal cirri from chaetiger 3, of equal length, 1/3–1/2 of body width (Fig. 27A). Cirrophores on tentacular segment and first dorsal cirri present; cirrophores otherwise absent. All appendages cylindrical. Parapodial lobes rounded conical, small. Anterior chaetigers with 2 aciculae, 1 in median and posterior. Chaetal fascicle with 6–9 compounds in anterior chaetigers, 4–5 in me

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)0,000
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 enseignants0,014
Score d'incertitude au seuil0,048

Scores du classifieur distillé par catégorie (deux têtes)

CatégorieCodexGemma
Métarecherche0,0000,000
Méta-épidémiologie (sens strict)0,0010,000
Méta-épidémiologie (sens large)0,0000,000
Bibliométrie0,0010,001
Études des sciences et des technologies0,0010,001
Communication savante0,0000,001
Science ouverte0,0000,001
Intégrité de la recherche0,0000,001
Charge utile insuffisante (le modèle a refusé de juger)0,0140,004

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 Opus0,043
Tête enseignante GPT0,225
Écart entre enseignants0,182 · 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
Publié2004
Routes d'admission1
Résumé présentoui

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