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Enregistrement W6968818287 · doi:10.5281/zenodo.5593006

Parabezzia Malloch

2014· article· en· W6968818287 sur OpenAlexaboutno aff

Notice bibliographique

RevueZenodo (CERN European Organization for Nuclear Research) · 2014
Typearticle
Langueen
DomaineAgricultural and Biological Sciences
ThématiqueVector-Borne Animal Diseases
Établissements canadiensnon disponible
Organismes subventionnairesnon disponible
Mots-clésSensillumSetaDorsumTarsus (eyelids)AppendageAir sacs

Résumé

récupéré en direct d'OpenAlex

Parabezzia Malloch (Figs. 16A–B, 20K–L, 25H, 30E, 33A, 37B, 44R–S, 50B, 62B–C, 74L, 75A) DIAGNOSIS: Only pupa of Ceratopogonidae with a well-developed prothoracic extension (Fig. 25H) and the mesonotum with only 2 setae (D-1-T, D-2-T) and D-3-T (campaniform sensillum) (Fig. 30E). Also, only pupa of Ceratopogonidae with a well-developed prothoracic extension (Fig. 25H) and the abdominal segment 4 with 9-10 sensilla (Figs. 62 B-C) (lacking D-3-IV, L-1-IV, L-4-IV, V-7-IV and, in some, D-9-IV). DESCRIPTION: Total length = 1.50–2.59 mm. Without larval exuviae retained on abdomen. Exuviae with flagellum appressed against lateral margin of face, midleg, wing (Figs. 16A–B, 33A). Ecdysial tear medial to antennal base (as in Figs. 15D, 79D) or tearing into eye, either posteriorly or posterolaterally (Figs. 16A–B, 79F). Head: Dorsal apotome (Figs. 20K–L), without ventral line of weakness, without dorsomedial tubercle, without central dome; dorsolateral cephalic sclerite (as in Fig. 13H) fused to scutum, each side separated medially by dorsal apotome in whole pupa; mouthparts (Fig. 25H) with mandible well-developed, lacinia absent; palpus extending posterior to posterolateral margin of labium; labium entire (not divided medially); apex of antenna (Fig. 37B) equal to posterior to, posterior extent of midlength portion of midleg (portion lateral to mesosternum), narrowed posteriorly; sensilla: dorsal apotomals (Figs. 20K–L)—1 short seta, 1 campaniform sensillum; dorsolateral cephalic sclerite sensilla—1 very short seta, 1 campaniform sensillum or 2 setae (only in P. petiolata); clypeallabrals (Fig. 25H)—absent or 1 short peg; oculars (Fig. 25H)—1 campaniform sensillum. Thorax: Prothoracic extension (Fig. 25H) wide, well-developed, extending from palpus to antenna; mesonotum with or without welldeveloped moderately sized tubercles, not extending posteromedially, with or without slight protuberance, not dividing metathorax medially (Fig. 50B); respiratory organ (Figs. 44R–S) length/width = 1.95–2.82, short, squat, somewhat flattened dorsoventrally, with pores closely abutting at apex of respiratory organ, arranged in single row, outer surface with some wrinkles, with or without short, wide pedicel, base with short posteromedial apodeme, membranous base of respiratory organ short, tracheal tube straight to slightly curved along length, with annulations to half length; wing (Fig. 37B) with apical tubercle lateral to apex of hind leg, separated medially by fore-, midlegs; halter apex and hind leg (Fig. 33A) broadly abutting; halter apex abutting anterolateral knob-like extension of tergite 2; legs (Fig. 37B) with lateral margin of foreleg near midlength of wing with abrupt angle or evenly curved; hind leg visible at lateral margin of wing (Fig. 33A); with apex of foreleg slightly to moderately anterior to apex of midleg; apex of hind leg abutting apex of midleg laterally; sensilla: anteromedials—1 very short seta, 1 campaniform sensillum; anterolaterals—1 short seta; dorsal setae (Fig. 30E)—D-1-T, D-2-T peg-like setae, D-3-T campaniform sensillum; D-2-T, D-3-T on single tubercleor closely approximated tubercles; supraalar 2—campaniform sensillum; metathoracics (Fig. 50B)—2 campaniform sensilla; M-3-T near anterior margin of metathorax. Abdomen: with 2 spots medially on tergites 1-7 or tergites 1-3 and fading posteriorly, segment 2 as wide or slightly wider than segment 3, segments with undivided, peg-like or thin to thick setae, with rounded to pointed or apically toothed, short to moderately elongate tubercles, tergites or sternites entire, not membranous or sternites 4-7 or 4-8 each with narrow membranous disc; segment 9 (Figs. 74L, 75A) not strongly modified, terminal processes closely approximated basally, each projecting nearly posteriorly to posterodorsolaterally, tapering to pointed apex; sensilla: tergite 1 (Fig. 50B) with 5 setae, 2 campaniform sensilla or 7 setae, 2 campaniform sensilla, including 4 lateral sensilla, D-2-I present, D-3 absent, D-7-I situated anterolaterally near L- 1-I; segment 4 (Figs. 62 B-C)—D-2-IV peg-like seta on short to moderately elongate tubercle, D-3-IV absent; D-5- IV peg-like seta, D-8-IV, D-9-IV (when present) short setae; only D-8-IV on short tubercle or D-5-IV, D-8-IV, D-9- IV on moderately elongate, separate tubercles, posterior dorsal sensilla in transverse row, arranged medially to laterally: D-5-IV, D-4-IV, D-8-IV or D-5-IV, D-4-IV, D-8-IV, D-9-IV; L-1-IV absent, L-2-IV, L-3-IV short setae on pointed or toothed tubercles, L-4-IV absent, V-5-IV, V-6-IV short setae, V-5-IV without tubercle or on short toothed tubercle, V-6-IV on short toothed or pointed tubercle,V-7-IV absent; segment 8 without D-3-VIII, without L-1-VIII; segment 9 (Figs. 74L, 75A)—with D-5-IX, D-6-IX campaniform sensilla. DISTRIBUTION AND HABITAT: The genus Parabezzia is known from 40 species from nearly every Region worldwide but absent from most of the Palaearctic (only in north Africa) and the Australasian Region (Borkent 2014). Pupae have been collected on the edges of streams, rivers and ponds. Grogan & Wirth (1977a) reported that P. alexanderi pupae were the most common of all ceratopogonids at a lily pond in Maryland, USA. TAXONOMIC DISCUSSION: There are seven species of Parabezzia known as pupae (Tables 2–3). There are two quite different types of pupae in this genus. One has numbers of rounded tubercles (Figs. 33A, 62B), the other, called the alexanderi group, has sharp tubercles (Fig. 62C) and abdominal sternites with membranous discs (e.g. P. alexanderi, P. balseiroi). All species of Parabezzia have reduced numbers of sensilla on every part of the body (see diagnosis). Some species have no clypeal-labral setae (P. bystraki, P. stagni) while others have a single peg (P. huberti, P. alexanderi, P. downesi, P. petiolata, P. balseiroi), a condition unique in the family. Grogan & Wirth (1977a) provided a key to the pupae of the four Nearctic species known at that time and Wirth & Grogan (1981) included a key to three species at Plummer's Island, Maryland, USA, including the newly described pupa of P. bystraki. Harris (1981) and Elson-Harris (1990) described the pupa of " Ceratopogon sp. n. 1" from Australia which would fit the diagnosis and distinctive description of Parabezzia here (the reared adult was not subsequently described). The described presence of eight sensilla on abdominal segment 4 (she likely missed the small campaniform sensilla D-4-IV and D-7-IV, hence a total of 10) is unique within the Ceratopogoninae for Parabezzia. However, at present there are no Parabezzia otherwise known from the Australasian Region. One potential candidate may be Heteroceratopogon, a genus related to Parabezzia and present in Australia. Unfortunately, the original material has been lost (Marlene Elson-Harris, pers. comm. 1993). If Harris (1981) correctly associated the larvae with the pupa and the above reidentification is correct, she provides the only larval description of a species of Parabezzia (or the only known larva and pupa of Heteroceratopogon). Grogan & Wirth (1977a) illustrated the dorsal apotomes of species of Parabezzia with DA-2-H being a very short seta but reexamination of original material indicates that these are campaniform sensilla, as in nearly all other Ceratopogonidae. Previous descriptions (Table 2) missed D-7-IV (campaniform sensillum) on abdominal segment 4. MATERIAL EXAMINED: P. alexanderi: 1 pupal exuviae, Lakeland Pond, College Park, Prince George’s County, Maryland, USA, 11-VI-1975 (USNM); 3 pupal exuviae, as previous locality, 27-V-1975 (2 WLGC, 1 CNCI); 2 pupal exuviae, as previous locality, 30-V-1975 (1 USNM, 1 CNCI). P. balseiroi: 2 pupal exuviae (of paratypes), Santa Ana, Entre Rios, Argentina, 9-XI-1984 (MLPA). P. bystraki: 1 pupal exuviae, Patuxent Wildlife Rescue Center, Prince George’s County, Maryland, USA, 20-VII-1976 (USNM). P. downesi: 9 pupal exuviae (of paratypes), Algonquin Park, Ontario, Canada, 8-VI-1960 (3 CNCI, 6 USNM). P. eupetiolata: 1 pupal exuviae (of paratype), 1 pupal exuviae (of allotype), Glenfield, Independence River, Lewis County, New York, USA, 22-VI- 1963 (USNM). P. huberti: 1 pupal exuviae, Patuxent Wildlife Rescue Center, Prince George’s County, Maryland, USA, 20-VII-1977 (USNM); 4 pupal exuviae (of paratypes), Falls Church, Virginia, USA, 22-VII-1951 (USNM); 2 pupal exuviae (of paratypes), Mount Solon, Virginia, 4-VII-1951 (USNM). P. stagni: 1 pupal exuviae (of holotype), Doornpan, Bulge River, North Transvaal, South Africa, 6-XI-1973 (NMSA). P. sp.: 1 pupal exuviae, 5 km E of Dandy, Vermont, USA, 25-VI-1986 (CNCI).

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 distillée sur la base complète

Imitation des enseignants

Ni prévalence calibrée, ni vérité terrain. Validation humaine à venir. Apprise à partir de 10 348 étiquettes directes de Codex et de 10 348 étiquettes directes de Gemma. Le mode candidate est l'union des têtes enseignantes seuillées; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont ni des étiquettes humaines ni des étiquettes directes de modèles de pointe.

score de la tête « metaresearch » (Codex)0,000
score de la tête « metaresearch » (Gemma)0,000
Version: codex-gemma-dda1882f352aStatut de validation: machine_predicted_unvalidated
Catégories candidatesÉtudes des sciences et des technologies, Charge utile insuffisante (le modèle a refusé de juger)
Catégories consensuellesCharge utile insuffisante (le modèle a refusé de juger)
DomaineSignal candidat: aucune · Signal consensuel: aucune
Devis d'étudeSignal candidat: Sans objet · Signal consensuel: aucune
GenreSignal candidat: Empirique · Signal consensuel: Empirique
Score de désaccord entre enseignants0,761
Score d'incertitude au seuil1,000

Scores Codex et Gemma par catégorie

CatégorieCodexGemma
Métarecherche0,0000,000
Méta-épidémiologie (sens strict)0,0000,000
Méta-épidémiologie (sens large)0,0000,000
Bibliométrie0,0000,000
Études des sciences et des technologies0,0010,000
Communication savante0,0000,000
Science ouverte0,0010,000
Intégrité de la recherche0,0000,000
Charge utile insuffisante (le modèle a refusé de juger)0,0230,011

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 Opus0,032
Tête enseignante GPT0,216
Écart entre enseignants0,184 · 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; les deux têtes enseignantes s’accordent sur ce qui est montré ici.

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
Publié2014
Routes d'admission1
Résumé présentoui

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