Heriades leavitti Crawford 1913
Bibliographic record
Abstract
Heriades leavitti Crawford, 1913 (Figs. 2F, 18–19) Heriades leavitti Crawford, 1913. Some bees from the New Brunswick, with descriptions of a new species of Heriades. The Canadian Entomologist:270. Type locality: Nerepis, New Brunswick. Type in USNM. Heriades crawfordi Graenicher, 1928:281. Neotrypetes truncates Robertson, 1929:131. Diagnosis. T3 with punctation medium-sized (0.7 times DOP as on scutum), and sparse punctures (1 time DOP) (Fig. 3J); tergal fasciae with rows of thin, white hairs (Fig. 3L); wings usually dusky. Male: large ocelli (Fig. 3C); posterior side of malar area rounded, not produced to angle; posterior margin of S5 with two rectangular lobes, with two rounded tufts of capitate hairs directed inward, and simple short hairs directed outward, with transverse subapical line (Fig. 19E); S6 with posterior margin produced to right-angled apex, without blackish subapical margin, with two tufts of simple, short, thin hairs, directed downward (Fig. 19F). Female: apical margin of clypeus with two tubercles sided by others smaller and irregular shaped (Fig. 19C), similar to H. variolosa and H. cristina sp. nov., but different from first by having usually darker wings and by second for apical margin of clypeus straight, without emargination but with depression between tubercles and T3 with smaller punctation and dull integument. Additional material examined: MEXICO: San Luis Potosi, 601 m, 22.5775 -99.40138889, 20/V/1989, D. Yanega (KUNHM-ENT 1♀). Veracruz, Coatepec, 1200 m, 19.4451 -96.96448, G. Quintos (IEXA-INECOL 1♀ 2♂). Xalapa, 1110 m. 19.51586 -96.87426, 01, 25/XI/2021, G. Quintos (IEXA-INECOL 2♂), 1150 m, 19.51213 -96.94586, 10/IX/2021, G. Quintos (IEXA-INECOL 1♂), 1200 m, 19.51337 -96.91743, 10/IX/2021, (IEXA-INECOL 1♀). Yucatán, Celestún, 3 m, 20.859304 -90.397205, 26/03/1996, F. León, R. Rodriguez (CER-UADY 2♂), Reserva Estatal El Palmar, 6 m, 21.037079 -90.182137, 16/VII/2006 (CER-UADY 3♂). Cuncunul, 30 m, 20.6412 -88.296294, 14/III/1996, R. Rodriguez (CER-UADY 1♂). Dzan, 29 m, 20.388369 -89.469093, 13/V/1996, H. Contreras (CER-UADY 1♂). Dzliam de Bravo, Reserva Estatal Dzilam, 6 m, 21.5027272 -88.490851, 05/I, 10/V/2006, V. Gaumeri (CER-UADY 9♂). El Cuyo, 6 m, 21.515833 -87.678333, 24/V/1995, R. Tut, 11/I/1996, L. Novelo (CER-UADY 2♂). [Homún], Reserva Estatal Lagunas de Yalahau, 11 m, 20.653353 -89.216377, 14/I, 24/07/2006 (CER-UADY 2♂). La Sierra, 13 m, 21.197361 -87.719176, 15/VI/1995, S. Noreña (CER-UADY 1♂). [Mérida], Reserva Estatal Dzibilchaltún, 11 m, 21.094807 -89.597755, 07/XI/2006 (CER-UADY 1♂). Río Lagartos, 3 m, 21.596482 -88.157898, 26/V/1995, H. Moo (CER-UADY 1♂), 27/VII/1996 (CER-UADY 1♂). Ticul, 8 K N Ticul, 29 m, 20.39777 -89.536646, 11/V/1995, S. Noreña (CER-UADY 1♂). Distribution. This species is mainly present in the United States and Canada; however, we found records that extend the distribution to Mexico, along the Gulf of Mexico slope and Yucatán Peninsula. The records of Quintos-Andrade, et al. (2023) of H. variolosa from Mexico, Veracruz, Coatepec and Xalapa belongs to H. leavitti. These areas correspond to the Sierra Madre Oriental, Veracruzan and Yucatán Peninsula biogeographic provinces (Morrone et al. 2022) (Fig. 18). The altitudinal range is from sea level to 1200 m. Comments. This species is similar to H. variolosa; females of H. leavitti can be recognized by having greater DBP on scutum and dusky wings; and males can be easily recognized by having two tufts of simple, thin, short hairs on S6, not a few simple, scattered capitate hairs, and two rounded tufts of capitate hairs on S5, not one line.
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How this classification was reachedexpand
Full frame machine prediction
Teacher imitationNot 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.
Distilled classifier scores by category (both heads)
| Category | Codex | Gemma |
|---|---|---|
| Metaresearch | 0.000 | 0.000 |
| Meta-epidemiology (narrow) | 0.000 | 0.000 |
| Meta-epidemiology (broad) | 0.000 | 0.000 |
| Bibliometrics | 0.001 | 0.000 |
| Science and technology studies | 0.001 | 0.000 |
| Scholarly communication | 0.000 | 0.000 |
| Open science | 0.000 | 0.000 |
| Research integrity | 0.000 | 0.000 |
| Insufficient payload (model declined to judge) | 0.013 | 0.003 |
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.
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from itClassification
machine, unvalidatedMachine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.
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".