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Record W6931551151 · doi:10.5281/zenodo.5103076

Thamiaraea brittoni Gusarov 2003, comb. nov.

2003· article· en· W6931551151 on OpenAlexaboutno aff

Bibliographic record

VenueZenodo (CERN European Organization for Nuclear Research) · 2003
Typearticle
Languageen
FieldAgricultural and Biological Sciences
TopicColeoptera Taxonomy and Distribution
Canadian institutionsnot available
Fundersnot available
KeywordsHolotypeDeflationChampionship

Abstract

fetched live from OpenAlex

Thamiaraea brittoni (Casey, 1911a), comb. nov. (Figs. 11–14, 20– 23 in Hoebeke 1988 (as Th. lira); Figs. 1–8 in Hoebeke 1994 (as Th. paralira); Figs. 127–134 in this paper) Sableta (Fusalia) brittoni Casey, 1911a: 145. Atheta (Sableta) brittoni: Fenyes, 1920: 221 (as valid species). Atheta (Sableta) brittoni: Bernhauer & Scheerpeltz, 1926: 666 (as valid species). Atheta (Sableta) brittoni: Moore & Legner, 1975: 356 (as valid species). Fusalia brittoni: Seevers, 1978: 260 (as valid species). Thamiaraea lira Hoebeke, 1988: 21, syn. nov. Thamiaraea paralira Hoebeke, 1994: 1, syn. nov. Fusalia brittoni: Ashe in Newton et al., 2000: 370 (as valid species). Type material. Lectotype of Sableta brittoni (here designated): ♀, “Westville Ct.[Connecticut] 27 July 1905 W.E.Britton ”, “ Fusalia brittoni Csy. ”, “TYPE USNM 39146” (red label), “CASEY bequest 1925” (NMNH). Holotype of Thamiaraea lira: UNITED STATES: Pennsylvania: Adams Co.: ♂, Arendtsville, 24.v.1927 (S.W.Frost) (CUIC). Paratypes: UNITED STATES: Pennsylvania: Adams Co.: ♀ (allotype), Arendtsville, 10.v.1927 (S.W.Frost); ♀, ditto but 18.iii.1927; ♂, ditto but 7.vi.1927; ♂, ditto but 2.vi.1927; ♂, ditto but 10.v.1927; ♂, ditto but 24.v.1927 (CUIC). Holotype of Thamiaraea paralira: UNITED STATES: New York: Westchester Co.: ♂, Yonkers, in flowers of Calycanthus fertilis, 29.v.1938 (H.Dietrich) (CUIC). Paratypes: UNITED STATES: New York: Westchester Co.: 4♂♂, same data as the holotype; Mississippi: Pontotoc Co.: ♂, 1 mi. SE Ecru, pitfall trap in deciduous woods, 18.xii.1980 (W.H.Cross) (CUIC). Additional material. UNITED STATES: Connecticut: New London Co.: ♂, molasses trap, 9.vi.1974 (L.E. Watrous) (FMNH); Kansas: Douglas Co.: ♂, ♀, 7 km S Lawrence, ex fermenting sap flow, 30.viii.1992 (J.S. Ashe) (KSEM); New Jersey: Middlesex Co.: 5♂♂, 4♀♀, Avenel (FMNH); Ohio: Clark [?] Co.: ♂, “ Shadywilde Selma ”, Malaise trap, center of big woods, 19.v.1972 (R.S.Boone); ♂, ditto but corner of big woods, 1.vi.1971; ♀, ditto but 23.ix.1971; ♂, ditto but by creek, 3.ix.1968; ♂, ditto but 9.vii.1968; ♂, ditto but 6.vii.1968; ♀, ditto but 7.vii.1968; Franklin Co.: ♂, ♀, Columbus, Ohio State University woods, ex banana trap, 20–27.x.1979 (L.E.Watrous); 2♂♂, ♀, ditto but 28–31.x.1979 (FMNH); Pennsylvania: Northampton Co.: ♀, Easton, 30.ix.1932 (J.W.Green) (FMNH); CANADA: Ontario: Wentworth Co.: 2♂♂, 2♀♀, Stoney Cr., on rotted bananas in pitfall, 2.vi.1973 (H.Frania) (KSEM); Québec: ♀, Downey, 19.vi.1995 (SPSU). Diagnosis. See Hoebeke (1988 (as Th. lira), and 1994 (as Th. paralira )). Discussion. According to Hoebeke (1994), Th. paralira differs from Th. lira only in having a smaller body size, shorter teeth at the posterior margin of the male abdominal tergum 8, and a weaker medial swelling in the posterior half of the tergum. My examination of the types of both species confirmed that they are identical in the shape of the aedeagus. In one paratype of Th. paralira and in several specimens fitting the description of Th. lira (in details of the male tergum 8) the internal sac was everted, and rather elaborate sclerites of the internal sac (Figs. 133–134) were examined. No difference between the specimens was found. Within species, the shape of the aedeagus and the sclerites of internal sac are usually less variable than the shape of the male tergum 8. It is a common phenomenon in many groups of aleocharines for smaller male specimens to have less prominent secondary sexual features (e. g., in Stethusa dichroa (Gravenhorst, 1802) (cf. Figs. 24–26 in Gusarov 2003d); in Tropimenelytron americanum Gusarov, 2002e and Tr. californicum Gusarov, 2002e (Gusarov 2002e)). Considering that 1) the types of Th. lira and Th. paralira are identical in the shape of the aedeagus; 2) there is no gap between the male specimens with the sexual features fitting Th. lira on one side, and Th. paralira on the other (Figs. 127–132); 3) it is the smaller male specimens of Thamiaraea that have less pronounced sexual features on the tergum 8; 4) both morphs are sympatric and even were collected in the same samples (Hoebeke 1994); I synonymize Th. lira and Th. paralira. My examination of the lectotype of Sableta brittoni revealed that it in fact belongs to Thamiaraea and is conspecific with both Th. lira and Th. paralira. Thamiaraea brittoni is the valid name for this species. Unfortunately, Casey (1911a) misplaced this species in Sableta Casey, 1910a, a genus unrelated to Thamiaraea, and when Hoebeke (1988) published his review of Thamiaraea, he had no means of knowing that one species of Thamiaraea had already been described by Casey. Distribution. Thamiaraea brittoni is widely distributed in the eastern United States and Canada. It is known from Ontario, Québec, Connecticut, New York, New Jersey, Pennsylvania, Ohio, Wisconsin (Hoebeke 1994), Kansas, North Carolina (Hoebeke 1994) and Mississippi.

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)0.001
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 score0.058

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0020.001
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0030.002
Science and technology studies0.0020.001
Scholarly communication0.0010.003
Open science0.0010.001
Research integrity0.0010.002
Insufficient payload (model declined to judge)0.0170.010

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 head0.034
GPT teacher head0.211
Teacher spread0.177 · 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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Citations0
Published2003
Admission routes1
Has abstractyes

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