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Enregistrement W6968673264 · doi:10.5281/zenodo.4474182

Zagrammosoma multilineatum

2021· article· en· W6968673264 sur OpenAlexaboutno aff

Notice bibliographique

RevueZenodo (CERN European Organization for Nuclear Research) · 2021
Typearticle
Langueen
DomaineBiochemistry, Genetics and Molecular Biology
ThématiqueLepidoptera: Biology and Taxonomy
Établissements canadiensnon disponible
Organismes subventionnairesnon disponible
Mots-clésHolotypeSubgenusSubspeciesErebidaeTaxonomy (biology)Type (biology)

Résumé

récupéré en direct d'OpenAlex

Zagrammosoma multilineatum (Ashmead) (Fig. 34) Hippocephalus multilineatus Ashmead, 1888: vii. Holotype ♀ [examined]. Locality: USA, Kansas, Riley Co., coll. C. Marlatt, host: Phyllonorycter ornatella (Lepidoptera: Gracillariidae). Depository: USNM type no. 27286. Zagrammosoma multilineatum; combination by Ashmead, 1904: 354. Preoccupied by Hippocephalus Swainson, 1839 (synonym of Percis Scopoli, 1777, Scorpaeniformes: Agonidae). Zagrammosoma multilineata punicea Girault, 1911: 123. Subspecies lectotype designation by Frison, 1927: 221. Lectotype locality: Washington D.C., USA. Lectotype depository: INHS type no. 44,261. Synonymy by Burks, 1979: 985. Zagrammosoma multilineatum puniceum; justified emendation by Peck, 1951: 460. Zagrammosoma multilineatum multilineatum (Ashmead, 1888). Subspecies designation by Peck, 1963: 189. Zagrammosoma multilineatus multilineatus; incorrect spelling by Pottinger & Le Roux, 1971: 437. Cirrospilus multilineatus; combination by Kerrich, 1969: 198. Cirrospilus (Zagrammosoma) multilineatum; unjustified use of subgenus designation by DeSantis, 1979: 261. Zagrammosoma zebralineata De Santis, 1983: 10. Holotype ♀ [examined]. Locality: Colombia, Pradera, coll. E. Flores, 1982. Depository: MLPA. Synonymy by Evans, 1999: 452. Diagnosis. Zagrammosoma multilineatum possesses dark stripes or bands that extend from the posterior margin of the pronotum to the notaulus (Fig. 34D), a character not found in other species of Zagrammosoma. The remaining body and wing patterns are similar to several species, however, the dark stripe between the notaulus and pronotum is absent in Z. interlineatum (Fig. 23D, E) and does not fully extend to the notaulus in Z. americanum (Fig. 4D, E) and Z. galapagoense (Fig. 18D, E). The gaster color patterns are different in Z. crowei (Fig. 12) and Z. interlineatum (Fig. 23). The second funicular is subequal in Z. deliae, as opposed to longer than wide in Z. multilineatum. There is no median stripe on the lower face in Z. interlineatum (Fig. 23A), whereas this stripe is present in Z. multilineatum (Fig. 34A). Description. Female - body length 1.4–1.98 mm. Metallic luster on body absent. Scape yellow with black stripe dorsally. Lower face with median stripe present. Vertex with 2 stripes above compound eye. Gena posteriorly with dark stripes below compound eye. Occiput yellow with 2 dark, vertical stripes. Pronotum with median stripe complete; laterally with 2 black stripes. Prepectus yellow with dark stripe along dorsal margin. Mesoscutum with median stripe complete. Mesoscutellum yellow with three dark stripes. Propodeum yellow with black median carina, anterior and posterior margins, and diagonal line connecting anterior and posterior margins. Procoxa and mesocoxa yellow. Metacoxa yellow with black stripe basally. Profemur and mesofemur yellow. Metafemur with interrupted or uninterrupted stripe dorsally. Fore wing: basal band absent; cubital band present; parastigmal, stigmal, and postmarginal bands present, with perpendicular extension greater than that of stigmal apex; connection from stigmal band to postmarginal band absent. Hind wing hyaline. Gaster yellow with dark transverse stripes and median stripe that bifurcates posteriorly on Gt 1. Upper ocular sulcus present. Pedicel longer than wide. Funiculars symmetrical: first longer than wide (w:l = 0.51–0.66); second longer than wide (w:l = 0.64–0.89). Pronotum, in dorsal view, bell-shaped (w:l = 1.07–1.45) 3–4 pairs of setae along posterior margin. Mesoscutum reticulate; small, scattered setae present; intermediate setae absent. Mesoscutellum subequal or wider than long (w: l = 1.0–1.13); submedian grooves absent or present, but faint and shallow. Hind tibial spur distinctly shorter than basitarsus. Hind basitarsus subequal or shorter than second tarsomere (bst:2 nd = 0.83–1.0). Fore wing l:w = 2.25–2.71. Submarginal vein with 5–6 setae dorsally. Basal fold setose. Cubital fold setose. Admarginal setae present. Uncus shifted basally more than length of uncus. Male - as female, except: body length 0.82–1.25 mm; metafemur yellow or yellow with interrupted or uninterrupted stripe dorsally; cubital band absent or present; gaster completely yellow or yellow with dark median stripe and transverse stripe on posterior margin of Gt 5. Remarks. No other species has been as difficult to define as Z. multilineatum, as the color patterns on the body and wings can be similar to many species. Extensive examination of loaned material revealed Z. multilineatum as the dumping ground for the genus, and at least six unique species have been identified from specimens identified as Z. multilineatum (Z. americanum, Z. deliae, Z. galapagoense, Z. interlineatum, Z. intermedium, Z. talitzkii). Published records of Z. multilineatum are difficult to verify without direct examination of the specimens used in published papers, and therefore, I have not included additional host and locality records of specimens for species that I have not personally examined. I have digitally examined the holotype of Z. zebralineatum and specimens collected by E. Flores from the same location and same host, coffee leaf miner (Leucoptera coffeella), and agree with the synonymy (Evans, 1999). Hosts. Reared from a large number of coleopteran, dipteran, and lepidopteran leaf miners. See Table 3 for a full list of hosts. Coleoptera: Buprestidae. Diptera: Agromyzidae. Hymenoptera: Tenthredinidae. Lepidoptera: Bucculatricidae, Gelechiidae, Gracillariidae, Lyonetiidae, Pyralidae, Tischeriidae. Distribution. Nearctic: Canada (BC), USA (AZ, CA, IA, KS, LA, MA, MD, MO, NC, NJ, NM, PA, SD, TN, TX, VA, VI). Neotropical: Bahamas, Jamaica, Colombia, Costa Rica, Ecuador (Galapagos), El Salvador, Guatemala, Haiti, Honduras, Venezuela (Fig. 35). Etymology. Multilineatum is taken from Latin meaning having many lines. Type material examined. Paratype: same as holotype [1♀, USNM: UCRCENT425376]. Additional material examined: BAHAMAS: Eleuthera: Rainbow Bay, 23m, 25°20’31”N, 76°27’1”W, 11.xi–19.xii.1986, J. R. Wiley, malaise [1♀, CNC: CNC 508660 (D5890)]. Exuma: Simon’s Point, 7m, 23°31’52”N, 75°47’49”W, 15–20.v.1986, T.L. McCabe [1♀, CNC: CNC 508842]. Grand Bahama Island: Freeport, Xanadu Beach, 26°29’35”N, 78°42’10”W, 16.x.1982, D. M. LaSalle, sand dunes [1♀, ANIC: UCRCENT238603]. CANADA: British Columbia: Chase, Adams Rd, 388m, 50°55’18”N, 119°37’45”W, 12.vii.1986, H. Goulet, car-net [1♀, CNC: CNC 508879]. COLOMBIA: Caldas: Naranjal, 1400m, 4°58’14”N, 75°39’4”W, 15.viii.1994, C. Lopez-Vaamonde, host: Leucoptera coffeella [1♁ 3♀, ANIC: UCRCENT238679–82]. Valle del Cauca: Palmira, 1015m, 3°30’31”N, 76°19’11”W, 15.ix.1975, A. Saldarriaga, host: Scrobipalpula sp., host plant: Solanum saponaceum (now bonariense?) [1♀, USNM: UCRCENT425392]. Valle Pradera, 1300m, 3°25’3”N, 76°11’36”W, 1981, E. Florez, #8106, host: Leucoptera coffeella, host plant: Coffee [4♁ 2♀, UCRC: UCRCENT414310, 499011–15]. Valle Pradera, 1982, E. Florez, host: Leucoptera coffeella, host plant: Coffee [MLPA-holotype of Z. zebralineatum]. COSTA RICA: Guanacaste: Area de Conservación Guanacaste, Murcielago, 75m, 10°56’28”N, 85°40’52”W, 24.i–4.ii.1996, J. Ugalde, malaise trap [1♀, ANIC: UCRCENT238683]. PN Santa Rosa, Sector Murcielago, Playa Blanca, 10m, 10°56’0”N, 85°51’0”W, 21.xi.2007, J. S. Noyes [1♁, BMNH: NHMUK10734428]. Santa Rosa NP, 300m, 10°53’33”N, 85°46’0”W, 2.iii.1986 – 23.iii.1986, D. H. Janzen, SE-8-C [1♁, USNM: UCRCENT425375]. Santa Rosa NP Hacienda (2C), 300m, 10°53’33”N, 85°45’59”W, 21.ii–14.iii.1987, D. Janzen, I. Gauld [1♀, BMNH: NHMUK10734425 (D5329)]. ECUADOR: Galapagos: Española Island, North Playa, 5–20m, 1°20’57”S, 89°41’51”W, 27.iv.1991, J. Heraty, arid zone, H91-002 [1♁ 9♀, UCRC: UCRCENT436418–436427]. Genovesa Island, Bahia Darwin, 20m, 0°19’8”N, 89°56’55”W, 10–27.iii.1992, S. Peck, Bursera forest, FIT, 92-14 [1♀, UCRC: UCRCENT410517]. Isabela Island, Alcedo, NE Playa, 0m, 0°20’40”S, 91°02’50”W, 26.vi.1991, J. Heraty, arid ravine, H91-120b [2♀, UCRC: UCRCENT491727, 491728]. Marchena Island, Punta Espejo, 0°18’54”N, 90°24’33”W, 11–24.iii.1992, S. Peck, 92-19 [1♀, UCRC: UCRCENT410522]. Pinzon Island, 2.5 km W. Pl. Escondida (5km on label), 280m, 0°36’14”S, 90°40’13”W, 19.vi.1991, J. Heraty, arid forest, H91-101 [3♀, UCRC: UCRCENT491724–26]. Santa Cruz Island, 1.5 km N. Bellavista, 280m, 0°40’55”S, 90°19’25”W, 1.vii.1991, J. Heraty,agricultural, H91-124 [1♀, UCRC:UCRCENT491721]. 13 km N. Santa Rosa, 300m, 0°34’6”S, 90°20’43”W, 1–30.iv.1992, S. Peck, arid zone, Bursera forest, FIT, 92-81 [1♀, UCRC: UCRCENT410519]. 6 km N. Los Gemelos, 300m, 0°34’37”S, 90°20’42”W, 17.v.1991, J. Heraty, low transition, H91-039 [1♀, UCRC: UCRCENT491722]. Santiago Island, 12 km E. Playa Espumilla, 725m, 0°13’54”S, 90°46’3”W, 5.vi.1991, J. Heraty, elfin forest, H91- 078 [1♁ 1♀, UCRC: UCRCENT491714, 491715]. EL SALVADOR: San Salvador, 690m, 13°42’29”N, 89°12’25”W, 18.v.1953, P.A. Berry, host: Leucoptera coffeella [2♀, USNM: UCRCENT425413, 425414]. GUATEMALA: West Guatemala, 460m, 14°33’2”N, 91°26’10”W, G. Manglitz, (Could be anywhere in “West Guatelama”), 51-6316, host: Leucoptera coffeella [6♁ 7♀, USNM: UCRCENT425379–91]. Retalhuleu: San Sebastian, 312m, 14°33’38”N, 91°39’12”W, ii–iii.1951, Oakley-Roberts, 51-2862, host: Leucoptera coffeella, host plant: Coffee [1♀, USNM: UCRCENT425416]. HAITI: 18°35’52”N, 72°11’45”W, 14.ii.1936, F. Sein Jr., Det. Lot No. 36- 4880, host: Leucoptera coffeella [2♁ 8♀, USNM: UCRCENT425402–10, 425412]. HONDURAS: Atlantida Dept.: La Ceiba, 15°46’7”N, 86°47’32”W, 6.vi.1991, R. Cave, host: Gracillaridae, host plant: Gliricidia sepium [1♀, ANIC: UCRCENT238605]. JAMAICA: Saint Andrew Parish: College Common, 173m, 17°59’54”N, 76°44’53”W, 1984, CIBC Trinidad Lot 5, CIE A16067, host: Leucoptera coffeella [1♀, BMNH: NHMUK10370145]. MEXICO: Baja California Sur: Las Barracas, 975m, 23°28’25”N, 109°27’8”W: 15.iv.1984, P. DeBach, Pan trap [1♀, UCRC: UCRCENT499001]; 17.iv.1985, P. DeBach, Pan trap

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: aucune
Score de désaccord entre enseignants0,010
Score d'incertitude au seuil0,032

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
Bibliométrie0,0010,000
Études des sciences et des technologies0,0010,000
Communication savante0,0000,001
Science ouverte0,0000,001
Intégrité de la recherche0,0000,000
Charge utile insuffisante (le modèle a refusé de juger)0,0100,003

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 Opus0,024
Tête enseignante GPT0,239
Écart entre enseignants0,215 · 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
Publié2021
Routes d'admission1
Résumé présentoui

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