Arganthomyza carbo Rohacek & Barber 2013
Notice bibliographique
Résumé
Arganthomyza carbo Roháček & Barber, 2013 (Figs 66–68, 70–84, 164) Arganthomyza carbo Roháček & Barber, 2013: 13. Type material. HOLOTYPE: ♂, “CAN:ON: SSMarie, Base-line Rd., 26.vi.2005, KNBarber, sweeps, Aster, Rubus, Equisetum, Carex, ferns, under aspen 46°31.40'N 84°24.40'W ” and “ HOLOTYPUS ♂, Arganthomyza carbo sp.n., J. Roháček & K. N. Barber det.2011” [red label] (DEBU, intact, see Fig. 164). PARATYPES: 121 ♂♂ 126 ♀♀ (AMNH, CASC, CNCI, DEBU, LACM, LEMQ, SEMC, SMOC, USNM) (details in ROHÁĆEK & BARBER 2013). Other material examined (not included in type series). 1 ♀ (used for molecular analysis, details in ROHÁĆEK & BARBER 2013). Additional records. CANADA: ONTARIO: Moosonee, 51°16.54'N 80°39.00'W, sweeps, Equisetum, Rubus, Cornus, graminoids, edge of wet forest trail, 10.vii.2014, 1 ♀; Moosonee, 51°16.33'N 80°39.11'W, sweeps, mostly Rubus, Impatiens, under Salix, Alnus, 10.vii.2014, 1 ♀, 11.vii.2014, 1 ♂, all K. N. Barber leg. (all CNCI); S[ault] S[te.] Marie, Baseline Rd., 46°31.40'N 84°24.40'W, sweeps, mostly ferns under aspen, 27.vii.2012, 1 ♂ 1 ♀, sweeps, Aster, Rubus, Equisetum, Carex, ferns, under aspen, 24.viii.2013, 1 ♂, K. N. Barber leg. (INHS). QUEBEC: Mt. Orford, 1200–2000', 21.vii.1968, 1 ♀, J. R. Vockeroth leg. (CNCI); Ste.-Anne-de-Bellevue, 19.vi.1973, 1 ♀, W. Boyle leg. (LEMQ). UNITED STATES OF AMERICA: NORTH CAROLINA: Spruce Mt., Smoky Park [GSMNP], 10.vi.1970, 1 ♀, FFS & JEW leg. (UGCA). Diagnosis. Male 2.06–3.14 mm, female 2.32–3.55 mm. Primarily blackish brown to black species (Figs 66–68, 164), very sparsely dark grey microtomentose and distinctly shining; postgena, ventral margin of gena and of occiput entirely blackish; face greyish brown; haltere, parafacialia entirely and anterior portion of frons, ventral corner of sternopleuron and large portions of antennae, mouthparts, gena, legs contrasting ochreous, yellow or whitish yellow; in female, mouthparts with clypeus distinctly darker and palpus brown and nrst antennal nagellomere dorsobasally darker. Frontal triangle very long, reaching anterior margin of frons. Mid basitarsus with 1–2 short dark setae and hind basitarsus with 2–3 (1–2 longer and thicker) short thickened setae. T1 and T2 completely fused to form syntergum T1+2, with only fusion line indicated. Wing hyaline (Fig. 84). Male genitalia (Figs 70–76). Epandrium (Figs 70, 71) blackish brown, slightly higher than long. Gonostylus (Figs 70, 71, 76) broad and nat, brown, of ham-shaped outline. Postgonite prolonged and strongly curved, sickle-shaped (Fig. 72); caudal process of transandrium reduced (Fig. 73). Female postabdomen and genitalia (see Figs 77–83 for details). T7 and S7 completely fused into dark brown ring-shaped tergosternum (Figs 78, 79). Ventral receptacle (Fig. 77) arched, wrinkled with distal fourth or nfth smooth with slender nnger-like projection at apex (similar to that in other members of the A. setiplanta group). Spermathecae (1+1) irregularly ovoid (slightly bent), both of similar size or one slightly larger (Fig. 81), with nnely ringed surface except for plain basal fourth and 7–8 spine-like appendages around duct insertion; cervix pale-pigmented, separate. For detailed description see ROHÁĆEK & BARBER (2013). Discussion. Arganthomyza carbo is the only Nearctic representative of the A. setiplanta group which otherwise includes A. setiplanta from Nepal and A. versitheca from Korea. Based on genitalic and postabdominal characters, A. carbo seems to be most closely allied to the Korean species A. versitheca (cf. ROHÁĆEK & BARBER 2013). Arganthomyza carbo can be safely distinguished from most other Nearctic congeners (except A. vittipennis with patterned wings) by its completely black occiput and postgena, its hind and mid basitarsus with 1–2 short proximoventral dark setae, abdominal T1 and T2 completely fused, and many genitalic characters of which the most salient are mentioned in the key and in the above diagnosis. Biology. Like all other species of the genus, little is known about the biology of A. carbo. Habitats where this species has been collected can be generally described as mesic mixed woodland (often dominated by trembling aspen, Populus tremuloides Michx. in Ontario, see Fig. 69) in openings or edges of trails where thick and diverse undergrowth communities thrive. It is our suspicion that ferns are at least indicators of suitable habitat for A. carbo and possibly also more generally for A. vittipennis, A. bivittata and A. duplex, which can also co-occur with A. carbo, especially the more common A. vittipennis and A. duplex (see Biology section of latter species and comments about ferns above in discussion of wing pattern and its signincance). Collections of adults have been made as early as 1 June (Quebec: Magog) and as late as 18 September (Ontario: Sault Ste. Marie). Distribution. Generally distributed in northeastern North America (Canada: Newfoundland, Nova Scotia, Ontario, Quebec; United States of America: Maine, Massachusetts, New Hampshire, New York, North Carolina, Tennessee, Virginia, West Virginia) with two specimens from western Canada (Alberta: Edmonton) (ROHÁĆEK & BARBER 2013, see Table 2, Figs 599, 604).
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 | 0,000 |
| Méta-épidémiologie (sens strict) | 0,001 | 0,000 |
| Méta-épidémiologie (sens large) | 0,000 | 0,000 |
| Bibliométrie | 0,001 | 0,001 |
| Études des sciences et des technologies | 0,002 | 0,001 |
| Communication savante | 0,001 | 0,001 |
| Science ouverte | 0,000 | 0,001 |
| Intégrité de la recherche | 0,001 | 0,001 |
| Charge utile insuffisante (le modèle a refusé de juger) | 0,013 | 0,004 |
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.
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 ».