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Record W6893935107 · doi:10.5281/zenodo.5952498

Oospila pipa Lindt & Hausmann & Viidalepp 2018, sp. n.

2018· article· en· W6893935107 on OpenAlexaboutno aff

Bibliographic record

VenueZenodo (CERN European Organization for Nuclear Research) · 2018
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicLepidoptera: Biology and Taxonomy
Canadian institutionsnot available
Fundersnot available
KeywordsAmazon rainforestPopulationIdentification (biology)Statistical analysis

Abstract

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Oospila pipa sp. n. (Figs 27, 61, 82) Oospila miccularia: sensu Cook & Scoble (1995 partim) nec Guenée, 1858: material from Ecuador and Peru. Holotype: ♂, Ecuador, Sucumbios prov., Panayacu riv., 13– 19.10.1999, 210 m, 00°23'S, 76°11'W (A. Lindt) (slide 277; TAMZ 0094294; DNA barcode LepNeotr 01875_NGS). Paratypes: 1♂, Peru, Lagunas, 01– 03.12.2003, 134 m, 05°14'15"S, 75°35'44"W (slide 8189) (A. Lindt); 1♂, Peru, Lagunas, 29.11. 2003, 120 m, 05°14'15"S, 75°35'44"W (slide 334) (A. Lindt); 6♂ 1♀, Ecuador: Napo prov., Puerto Misahualli, 5– 9.11.2002 (slide 310) (A. Selin, T. Armulik); 1♂ Ecuador, Zamora Chinchipe prov., Zamora, 19.04.2007, 1000 m, 04°06'30"S, 78°57'49"W (A. Lindt) (slide 509); 1♂ Ecuador, Zamora Chinchipe prov., Los Ecuentros, 21.04.2007, 1460 m, 03°48'47"S, 78°36'39"W (A. Lindt); 3♂, Ecuador, Sucumbios prov., Panayacu river, 13– 19.10.1999, 210 m, 00°23'S, 76°11'W (T. Kesküla) (slide 6615); 3♂ 2♀, the same data but A.Lindt leg. (slides 278, 336, 450); 1♂, Ecuador, Napo prov., Huabuno riv., 03.– 06.10.1999, 400 m, 00°50'S, 77°15'W (A. Lindt); 1♂, Peru, Santa-Rosa, 19.11. 2003, 800 m, 09°58'36"S, 75°30'23"W (slide 278) (A. Lindt); 1♂, Ecuador [Orellana prov.], Rio Shiripuno-Via Auca, 200 m, 27– 28.10.2002, 76°46'W, 01°06'S (slide 503)(I. Renge); 1♂, Ecuador, Orellana prov., Rio Shiripuno, 27.10.2002 (I. Renge); 1♂ 1♀, Ecuador, Orellana prov., Rio Shiripuno, 27– 31.10.2002 (slide 449, 450) (A. Selin, T. Armolik); 1♂, Ecuador, Orellana prov., Rio Shiripuno, 26.10.2002 (A. Selin, T. Armolik); 1♂, Ecuador, Orellana prov., Rio Shiripuno, 31.10.2002 (A. Selin, T. Armolik); 1♂, Venezuela, Orinoco river, 20.10.1999 (slide 309) (A. Selin & T. Armulik); 1♂, Venezuela, about 150 km to E of Puerto Ayacucho, 23.10.1999 (A. Selin & T. Armulik). 1♂, Colombia, Moona, Terr. Caquetà (W. Hopp; ZSM) (slide ZSM G 17493); 19♂ ♀, Peru, Huanuco, Panguana, Rio Llullapichis, 260m, E tributary Rio Pachitea, -9.6138° / - 74.9353°, 13.11.– 13.12.2008 / 23.09.– 02.10.2004 / 02.– 18.10.2009 / 01.– 30.04.2012 / 20.09.– 08.10.2012 / 24.02.– 10.03.2013 / 20.09.– 04.10.2013, 20.05.– 10.06.2014 (A. Segerer, E.G. Burmeister, G. Riedel, E. Diller, H. Sulak, O. Vasha; ZSM) (DNA Barcode BC ZSM Lep 66259; genitalia slides ZSM G 15117, 15782, 20343); 1♂, id., 21.07.2013 (leg. et coll. A. Moser) (DNA barcode BC ZSM Lep 88272); 2♂ 1♀, Ecuador, Zamora-Chinchipe, Estaciòn biològica San Francisco, 19 / 20, 1020– 1025 m, ca. 04°07’ S, 78°58’ W, 19.– 24.11.2008 / 0 1.04.2011 (M. Adams, G. Brehm; coll. G. Brehm) (DNA barcodes ID 22693, 16092, 17069); 1♂, Ecuador, Zamora-Chinchipe, Bombuscaro, 1025 m, -4.1165°, -78.9815°, 19.11.2008 (leg. et coll. G. Brehm) (DNA barocde ID 16096); 1♂, Ecuador, Zamora-Chinchipe, Reserva Copalinga, 1213 m, -4.0883°, -78.9657°, 19.11.2008 (leg. et coll. G. Brehm) (DNA barocde ID 19008). The holotype will be deposited in the collection of EMNH (Tallinn), the paratypes in the collections of EMNH, IZBE, ZSM, and in private collections of G. Brehm, A. Moser, A. Lindt and A. Selin. Other material (not included into type series): 1♀, northern Brazil, [north-western Amazonas], Canal Maturaca, Mission Cauaburi, 70 m, 14.01.1963 (C. Lindemann; ZSM) (slide ZSM G 20342); 1♀, Brazil, [northeastern] Para, Belem-Gunma, Parque Ecologico do Gunma, 22m, -1.213°, -48.29°, 11.04.2010 (T. Decaens; BIO Guelph) (DNA barcode BC-INCT0359). Diagnosis. A member of the O. miccularia species group with large light orange brown blotches at the apex and the tornus of both wings, distinguished from related species by male genitalia, by the presence of a group of tangled, long spines dorsally to the apex of valva. The apical blotch of the fore wing is broad near costa. See the description of O. miccularia above. O. pipa is the allopatric sister species of O. miccularia, differing from the latter by the more extended patch of spines at the tip of the valva and by the much longer bursa copulatrix. Description. Wingspan, 15–18 mm in males, 17–21 mm in females (Fig. 27,). The frons is yellowish brown, the fillet white, the vertex yellowish, a red-brown line in between. The male antennae are bipectinate, the external and inner pectinations, on the fifth antennal segment, are 0.5–0.6 and 0.35–0.4 mm long, accordingly, in males, 0.35–0.5 mm and 0.25–0.35 mm long in females. The palpi project ahead of the frons by about 0.45–0.6 mm. The thorax is dorsally green, the abdomen mottled rose and whitish. The crests on tergites A1–A5 are reddish brown. The wings are dark green, the marginal blotches are light orange brown with irregular brown irroration. The marginal line is brown on both wings; the marginal blotches are edged by a thin white and a proximal grey line, which protrudes into the white line along some veins. The apical blotch of the fore wing reaches the costa broad and expands along the distal margin of the wing, reaching vein M3, and is connected with the tornal blotch by a narrow connection between the veins M3 and CuA1. The hind wing blotches are continuous along the distal margin of the wing but somewhat narrower than on the fore wing. The discal spots are present on both wings, small, vague, brown or green, sometimes also an anterior white discal dot is present on the hind wing. The fringe is pale brownish, chequered darker at vein ends. Male genitalia (Fig. 61): The socii are rounded, broader than in related species, and the gnathi are hooked. The juxta is short, provided with oval dorso-lateral projections and with a pair of short ventro-lateral projections. The valva is split, its saccular part refolded, with a finger-shaped projection directed dorsally and reaching beyond the costal edge of the valva. The distal part of the valva bears a subapical patch of long, tangled spines, not restricted to the edge as in O. miccularia. The aedeagus is provided with a sclerotized dorsal rib as in O. bifida sp. n. The sternite A8 has two, shallowly rounded lobes at its posterior edge. Female genitalia (Fig. 82): Similar to those of O. bifida sp. n. and O. brehmi sp. n., but the sterigma of O. pipa is less broad (1.0– 1.1 mm) than in O. brehmi, with paired, oval, horizontally furrowed lateral sclerites. The ductus bursae (2.0 mm), and corpus bursae (2.0 mm) are very long. The signum is medium-sized (width 0.35–0.45 mm, height 0.2 mm) and bicornute. Genetic data. BIN BOLD:AAG7368 (n=10 from Ecuador, Peru, Brazil). BIN intraspecific variation low in Ecuador, Peru and Bolivia (0.0%), but with a slightly diverging haplotype in Brazil /NW. Para (0.3%). Nearest neighbours: Sister species O. brehmi sp. n. and O. moseri sp. n. (described below), O. miccularia (1.3%). Although O. pipa and O. miccularia belong to the same BIN, O. pipa is described here at species rank, as the genetic distance is constant and well correlated to some differential features in genitalia. Etymology. The species name " pipa " is a free combination of letters, gender feminine. Biology. Oospila pipa is a widespread species in various tropical lowland and montane forests, collected from February to December. Distribution. Colombia, Venezuela, Ecuador, Peru, western Brazil (north-western Amazonas), possibly also prov. Para, requiring confirmation by dissection.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: none
Teacher disagreement score0.017
Threshold uncertainty score0.057

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0020.001
Science and technology studies0.0010.001
Scholarly communication0.0000.002
Open science0.0000.001
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0170.005

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.026
GPT teacher head0.241
Teacher spread0.215 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Published2018
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