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Enregistrement W7103889678 · doi:10.5281/zenodo.17514841

Cheilosia (Taeniochilosia) aenigmatosa Barkalov 1993, stat. rev.

2025· article· W7103889678 sur OpenAlexaff

Notice bibliographique

RevueZenodo (CERN European Organization for Nuclear Research) · 2025
Typearticle
Langue
DomaineBiochemistry, Genetics and Molecular Biology
ThématiqueProtist diversity and phylogeny
Établissements canadiensUniversity of Ottawa
Organismes subventionnairesnon disponible
Mots-clésScutellumSetaMargin (machine learning)Black male

Résumé

récupéré en direct d'OpenAlex

Cheilosia (Taeniochilosia) aenigmatosa Barkalov, 1993 stat. rev. Fig. 2 Cheilosia aenigmatosa Barkalov, 1993: 700. Cheilosia grisella Becker, 1894 – Stackelberg & Richter 1968: 246. — Peck 1988: 104. — Barkalov & Ståhls 1997: 28. — Gujabidze 2002: 245. — Mengual et al. 2020: 25. — Speight 2020a: 35. Cheilosia aenigmatosa – Barkalov 1993: 700. — Barkalov & Ståhls 1997: 52. — Barkalov & Mutin 2018: 486. Differential diagnosis Cheilosia aenigmatosa is identified as belonging to the subgenus Taeniochilosia by the combination of bare eye, black legs and the anterior process of lunula not broadly confluent with the face (Barkalov & Ståhls 1997). The male genitalia are figured in Barkalov (1993). The male of C. aenigmatosa is very similar to C. pollinifacies and can be distinguished as follows: posterior margin of scutellum with few and thin setae, diameter almost as thin as scattered black pile on disc of scutellum (Fig. 2E) (in C. pollinifacies the posterior margin of scutellum has multiple setae with a diameter much larger than diameter of scattered long black pile on disc of scutellum; Fig. 56E), scutum with dense erect short golden pile, with sparse long black erect pile intermixed (in C. pollinifacies scutum also with sparse long black pile, but short pile on scutum semi-adpressed, variable in colour, ranging from predominantly black to predominantly golden). Females of C. aenigmatosa differ from C. pollinifacies by the absence of black setae or pile on posterior margin of scutellum, while black setae are present on posterior margin of scutellum in C. pollinifacies. Genetically, it is similar to C. ouwehandae Bot sp. nov., but the male differs in many ways (the female of C. ouwehandae remains unknown): C. aenigmatosa is larger (body size usually at least 8 mm instead of 6.5 mm), face and parafacia densely pruinose (slightly pruinose in C. ouwehandae), facial tubercle less well developed, not further projecting than mouth edge (rounder, and further protruding, well beyond mouth edge in C. ouwehandae), postpedicel black (basoventrally orange in C. ouwehandae), frontal triangle with large proportion of yellow pile (pile black in C. ouwehandae), pile on scutum golden instead of whitish, and posterior margin of scutellum with black pile setae instead of black setae and abdomen with less dense pruinosity. Material examined Collected in 2018, 2019 and 2021, but 2018 records were not published in Mengual et al. (2020). Thus, all records are reported here. GEORGIA – Adjara Region • 1 ♀; Kintrishi Nature Reserve; 41.7619° N, 42.1162° E; 2462 m a.s.l.; 16 Jun.–30 Jun. 2018; GGBC-members leg; ZFMK, ZFMK-TIS-8010536 • 1 ♀; Kintrishi Nature Reserve; 41.7619° N, 42.1162° E; 2462 m a.s.l.; 30 Jun.–14 Jul. 2018; GGBC-members leg; ZFMK, ZFMK-TIS-8010398 • 1 ♀; Mtirala N.P.; 41.6535° N, 41.8730° E; 1106 m a.s.l.; 16 Jul. 2021; S. Bot leg.; BA, SB.003061. – Imereti • 2 ♂♂; road from Abastumani to Sairme; 41.824° N, 42.847° E; 2150 m a.s.l.; 10 Jun. 2019; F. Van de Meutter leg.; FMT • 1 ♂; Abastumani area, along path; 41.823° N, 42.840° E; 2025 m a.s.l.; 11 Jun. 2019; F. Van de Meutter leg.; FMT. – Mtskheta-Mtianeti • 1 ♂; Gudauri-pass; 42.5336° N, 44.4751° E; 2210 m a.s.l.; 11 Jul. 2019; A. Ssymank leg.; ASW, Ssy 9504- 01, ZFMK-TIS-8009412 • 1 ♀; same data as for preceding; ASW, Ssy 9504-02, ZFMK-TIS-8009413. – Samegrelo-Zemo Svaneti • 1 ♀; 43.0319° N, 42.8272° E; 1905 m a.s.l.; 13 Jun. 2019; X. Mengual leg; ZFMK, ZFMK-DIP-00066299 = ZFMK-TIS-8008764 • 1 ♂; 42.900° N, 42.934° E; 2700 m a.s.l.; 17 Jun. 2019; S. Bot leg.; SBA, SB.003064 • 1 ♀; 42.9140° N, 43.0911° E; 2575 m a.s.l.; 18 Jun. 2019; X. Mengual leg.; ZFMK, ZFMK-DIP-00066298 = ZFMK-TIS-8006837 • 1 ♂; 7 km W of Ushguli, near hilltop; 42.906° N, 42.937° E; 2615 m a.s.l.; 16 Jun. 2019; F. Van de Meutter leg.; FMT • 1 ♀; 7.5 km N of Mestia, path to glacier; 42.738° N, 43.113° E; 1800 m a.s.l.; 14 Jun. 2019; F. Van de Meutter leg.; FMT • 3 ♂♂; 43.0275° N, 42.9115° E; 2887 m a.s.l.; 14 Jul. 2021; S. Bot leg.; SBA, SB.003058 to SB.003060 • 2 ♀♀; same data as for preceding; SBA, SB.003056, SB.003057. – Samtskhe-Javakheti • 1 ♂; Borjomi N.P.; 41.824° N, 42.848° E; 2165 m a.s.l.; 10 Jun. 2019; S. Bot leg.; SBA, SB.003062 • 1 ♀; same data as for preceding; SBA, SB.003063. RUSSIA – Kabardino-Balkaria • 1 ♀; 43.4841° N, 43.1006° E; 1776 m a.s.l.; 6 Jun. 2018; A. Przhiboro leg.; ZFMK, ZFMK-DIP-00078649 = ZFMK-TIS-8009592 • 2 ♂♂; 43.4795° N, 43.0971° E; 1836 m a.s.l.; 7–8 Jun. 2018; A. Przhiboro leg.; yellow plates; ZFMK, ZFMK-DIP-00078658 = ZFMKTIS-8009602, ZFMK-DIP-00078660 = ZFMK-TIS-8009567 • 2 ♀♀; same data as for preceding; ZFMK, ZFMK-DIP-00078653 = ZFMK-TIS-8009596; ZFMK-DIP-00078659 = ZFMK-TIS-8009566; ZFMK. Genetics DNA barcodes of C. aenigmatosa were resolved into three clusters with high support (BS = 96.7–100%). DNA barcodes of European specimens of C. grisella were grouped together with high support (BS = 98.7%). See Remarks. Remarks Previous records of C. grisella from the Caucasus are referred here to as C. aenigmatosa and C. grisella is considered absent from the Caucasus Region. Barkalov & Ståhls (1997) synonymized C. aenigmatosa with C. pollinifacies without providing an explanation or comment. Our genetic study resolved C. pollinifacies and related species in several clusters. One group corresponds to the original description of C. pollinifacies and three other groups match the description of C. aenigmatosa, with C. ouwehandae sp. nov. branching in between (Supp. file 1: Fig. S1). Although genetically similar, C. ouwehandae differs from C. aenigmatosa morphologically (see Differential diagnosis). Within C. aenigmatosa, we could not find morphological differences between the genetic clusters. Here we reinstate C. aenigmatosa as a genetically and morphologically different species from C. pollinifacies. Biology During our expeditions, collected between 6 June and 16 July at an altitude between 1106 and 2887 m a.s.l. Behaviour difficult to ascertain due to confusion with the very similar C. pollinifacies with which it often co-occurs. At places where C. aenigmatosa was caught, individuals belonging to C. aenigmatosa or C. pollinifacies were often found in clearings in forest, along forest edges or near tall vegetation in alpine meadows, visiting low flowers including Caltha palustris L. and Ranunculus sp. Distribution Caucasus (Russia, Georgia).

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: Observationnel · Signal consensuel: aucune
GenreSignal candidat: Autre · Signal consensuel: Autre
Score de désaccord entre enseignants0,027
Score d'incertitude au seuil0,090

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
Bibliométrie0,0020,001
Études des sciences et des technologies0,0020,001
Communication savante0,0010,001
Science ouverte0,0010,001
Intégrité de la recherche0,0010,001
Charge utile insuffisante (le modèle a refusé de juger)0,0270,018

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 Opus0,017
Tête enseignante GPT0,236
Écart entre enseignants0,220 · 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'étudeObservationnel
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
Publié2025
Routes d'admission1
Résumé présentoui

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