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Enregistrement W6931326577 · doi:10.5281/zenodo.5073169

Peristenus broadbenti Goulet & Mason 2006, n. sp.

2006· article· en· W6931326577 sur OpenAlexaboutno aff

Notice bibliographique

RevueZenodo (CERN European Organization for Nuclear Research) · 2006
Typearticle
Langueen
DomaineMedicine
ThématiqueMosquito-borne diseases and control
Établissements canadiensnon disponible
Organismes subventionnairesnon disponible
Mots-clésHolotypeVoltinismAnimal ecologyGenusScapeNymph

Résumé

récupéré en direct d'OpenAlex

Peristenus broadbenti n. sp. (Figs. 4 habitus, 10, 16, 47, 52a, 52b, 58, 61, 62, 63, 85, Table 15) Type material. Type locality: Canada, Alberta, Lethbridge. Holotype, female (CNCI), labelled: [White] " Canada, Alberta, Lethbridge, Victoria Church, alfalfa­weed mix, Coll. 24.VII.2002 49º42.279'N 112º44.951'W C. Herle, Cage ID: 3D"; [White] "Lab. emg. 10.VI.2003 – 4.VII.2003 Ex. Lygus nymph"; [Red] " HOLOTYPE Peristenus broadbenti CNC No. 23478". Condition of holotype: Perfect. Allotype male from same locality and emergence date, but cage "ID: 11B". Paratypes: all specimens from above locality. Origin of species name. This species is named in honour of Bruce Broadbent who worked for many years on Lygus endoparasitoids. He reared several species, which benefited markedly our species concept for southern Ontario. Because all species he worked on in Ontario are named, this species is dedicated to him as acknowledgement for his long support of systematic research of mirid parasitoids. Diagnosis. Clypeus black or dark brown, Frons not densely punctate (especially between lateral ocellus and inner eye margin), forewing vein r generally developed and a univoltine life cycle associated with the second nymphal generation of Lygus. Description. FEMALE. Colour. Head and mesosoma black; metasoma black. Legs generally straw coloured, metacoxa brown to black; basal 0.3–0.5 of metatibia usually straw coloured or occasionally light reddish brown, and apical 0.5–0.7 of metatibia, metatarsomere 1 clearly darker than basal half of metatibia, but metatarsomeres 2–5 less dark than metatarsomere 1. Palpi, tegula and mandible (except apex) straw coloured. Scape to flagellomere 2 straw coloured, threafter brown to dark brown. Stigma dark brown and straw coloured in basal 0.3. See habitus (Fig. 4). Structure. Flagellum with 18–20 flagellomeres (respectively 3%, 59% and 35% of 32 specimens) and flagellomeres enlarged in apical 0.5. Few preapical flagellomeres subquadrate (none 60%, one 34% and two 6%). Length of gena behind eye 0.91–1.09 times as long as length of eye. Height of eye 1.30–1.42 times as long as minimum distance between inner eye margins (as in Fig. 18). Maximum width of head behind eyes subequal (0.91–0.96) to maximum head width at eye level. Occipital carina developed in dorsal third. Metasomal tergum 1 with lateral edges clearly convergent (posterior margin 2.2–2.3 times as wide as narrowest width near base) and elongate (medial length of tergum 1.5–1.8 times maximum width at posterior end). Radial cell length 0.94–1.06 as long as stigma width (Figs. 58, 61–63). Forewing vein r usually developed (85% based on 50 specimens) and short (Figs. 58, 61–63) and basal cell of forewing (except extreme base) pubescent (as in Fig. 54). Sculpture. Punctures on vertex 5–10 µm in diameter, on frons and mesoscutum about 10–15 µm in diameter (a little larger than diameter of ommatidia). Punctures 20–25 µm apart on vertex (especially between lateral ocellus and inner eye margin), 5–15 µm apart on frons to 5–10 µm apart near antennal socket, and 20–25 µm apart on mesoscutum. Punctures on mesopleuron generally dense, occasionally scattered. Clypeus generally smooth, rarely punctate over disc. Metasomal tergum 1 with about 10–12 longitudinal ridges, these often anastomosing on disc and forming a puncture­like sculpture. MALE. Colour. As in female. Structure. Flagellum with 20–23 flagellomeres (respectively 7%, 45%, 42% and 5% of 40 specimens) and flagellomeres narrow in apical 0.5. Height of eye 1.00–1.11 times as long as minimum distance between inner eye margins. Otherwise structure and sculpture as in female. Taxonomic notes. Among the species of the P. pallipes complex with a black or dark brown clypeus, P. broadbenti is nearest to P. gillespiei. Almost no structural differences were found between the two species. However, adults of the species differ in their life cycle and their almost allopatric range (narrowly sympatric in the Cascade Mountains). Though the data on reared specimens is limited, the Cascades samples from the Harrison Lake support the lack of gene flow between the two species. The emergence data from this locality are consistant with the typical P. gillespiei early emergence and the typical P. broadbenti late emergence. A summary of measurement differences between P. broadbenti and P.gillespiei is given in Table 15. Adults of P. broadbenti differ from those of P.howardi in the development of forewing vein r, the presence of males, and a univoltine life cycle. A summary of measurement differences between P. broadbenti and P. howardi is given in Table 15. Adults of P. broadbenti could easily be confused with those of P. braunae a darkly coloured species. They are easily distinguished from those of P. braunae by the colour of the clypeus and metatibia, by the puncture density on the vertex especially between the lateral ocellus and the inner eye margin, by the the ratio of eye height to minimal distance between eye inner margins, and the ratio of length of flagellum to maximum width of head between outer eye margins. Host and biological notes. Adults of P. broadbenti have been reared from various species of Lygus. Adults occur from late June till late August with peak abundance probably in mid July. This is a univoltine species. Females of this species parasitize nymphs of only the second generation of Lygus. Material examined and range. 116 (36♂, 80♀) adults were studied. Of these, 42 were reared from Miridae hosts and 74 were field collected. The species is known from temperate regions where two full Lygus generations occur from southwestern Alberta and southern British Columbia south to Nevada and Wyoming. CANADA. AB: Eisenhower jct. Banff Nat. Park (1♀); Johnston Canyon, vic. Banff (3♀); Hardstead (1♀); Hendrickson (1♀); Lethbridge (7♂, 9♀); Lethbridge, 49º42.279'N 112º44.951'W (22♂, 16♀); Lethbridge, Pavan Park, 49º45.294'N 112º50.525'W (1♂, 6♀); Rolling Hills (2♂, 6♀); Rosdal (1♀); Waklin (1♂, 2♀); Waterton Lakes Nat. Park, 1300 m (1♂, 6♀). BC: Diamond Head Trail, vic. Squamish, 1000 m (5♀); Hatzic Lake (3♀); Harrison Lake (1♀); Harrison Mills (1♀); MacGillivray Creek, vic. Chilliwack (1♀); Prince Rupert (1♀); Robson (1♂); Terrace (2♀); Summerland (1♀); West Harrison Rd., 49º16'26"N 121º52'41"W (2♀). USA. MT: Beaverhead Co., Clark Canyon Dam Rd. (1♀; ESUW). NV: 19 km SW Wells, 2700 m (1♀). OR: Lincoln Co., 13 km E Eddyville (6♀). WA: Lewis Co., Meskill, 1.6 km W Hwy. 6 (2♀); Pacific Co., Idwaco, 28 km N Hwy 101 (1♀). WY: Albany Co., Medecine Bow Nat. For., 0.8 km NE Lincoln Monument (1♀; ESUW); Albany Co., Medecine Bow Nat. For., 1.6 km N Lincoln Monument (1♀; E SUW); Albany Co., Medecine Bow Nat. For., 0.6 km S Lincoln Monument (1♀; ESUW); Albany Co., Pole Mtn. (1♀; ESUW); Battle Lake Rd., Sierra Madre Range (1♀; ESUW).

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: Autre · Signal consensuel: Autre
Score de désaccord entre enseignants0,026
Score d'incertitude au seuil0,052

Scores du classifieur distillé par catégorie (deux têtes)

CatégorieCodexGemma
Métarecherche0,0000,000
Méta-épidémiologie (sens strict)0,0000,000
Méta-épidémiologie (sens large)0,0000,000
Bibliométrie0,0010,001
Études des sciences et des technologies0,0020,001
Communication savante0,0000,001
Science ouverte0,0010,001
Intégrité de la recherche0,0000,001
Charge utile insuffisante (le modèle a refusé de juger)0,0120,004

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 Opus0,021
Tête enseignante GPT0,246
Écart entre enseignants0,225 · 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
GenreAutre

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
Publié2006
Routes d'admission1
Résumé présentoui

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