Belladonna barryi Klimaszewski and Chandler 2023, sp. n.
Bibliographic record
Abstract
243. Belladonna barryi Klimaszewski and Chandler, sp. n. Figs. 12a–g, Table 1 Holotype (male). USA, New Hampshire, Strafford Co.: Spruce Hole, 3 mi SW Durham, 1–17.VI.1990, G. Fortier and D.S. Chandler, FIT on mat. (CNC). Paratypes: USA, Maine, York Co.: West Lebanon, 7–13.V.1990, D.W. Barry, FIT, 1 female; 14–20.V.1990, D.W. Barry, FIT, 1 female; 5–9.VII.1990, D.W. Barry, FIT, 1 female. New Hampshire, Strafford Co.: Spruce Hole, 3 mi SW Durham, 12.V.1990, 15.VII.1990, G. Fortier, aquatic vegetation, 2 males, 1 female; 9–10.VI.1982, D.S. Chandler, window trap, 1 female; 20–25.V.1990, G. Fortier and D. Chandler, FIT, 1 male; 1–17.VI.1990, G. Fortier and D. Chandler, FIT on mat, 2 females. Durham, 25.IX.1915, 1 male. CANADA, Ontario, Rondeau Provincial Park, Tulip Tree Trail, 5.VI.1985, A. Davies and J.M. Campbell, ex Carex and moss on logs in pond (CNC), 3 males, 1 female, 2 sex? Rondeau Provincial Park, South Pt. Trail turnoff, 30.V.1985, A. Smetana (CNC) 1 male. 8 mi W White River, 14.VI.1973, Campbell and Parry (CNC) 2 males, 1 female, 1 sex? Bells Corners, 9.VI.1983, A. Davies and M. Vermette, berlese muskrat nest (CNC), 1 female. Hald.–Norfolk Reg., Cronmiller prop., 6 km W St. Williams, 42°40’21’’N, 80°29’26’’W, 20.VII.2011, Brunke and Paiero, forest, at lights, (DEBU), 1 male. Etymology. Named for Donald W. Barry, who collected many species for us in Maine at a site 3.5 km from the NH border, of which some have not yet been taken in New Hampshire. He is a former UNH MS graduate student and eventual Agriculture Extension Agent at the University of Maine, Orono, USA. Diagnosis. Male tergite VIII with four sharp apical teeth, two distributed laterally and two medially, median teeth smaller (Fig. 12c); apical part of median lobe of aedeagus broadly triangular, elongate and sinuate (Fig. 12b); spermathecal capsule pitcher-shaped in lateral view, stem swollen posteriorly (Fig. 12g). Description. Body length 3.21–3.79 mm, body broadly oval, moderately convex; color dark brown except paler (yellowish-brown) legs, two basal and two apical antennomeres, legs, posterior part of elytra and base of abdomen (Fig. 12a) (some northern specimens may be black); head distinctly narrower than pronotum (Fig. 12a); pronotum sub-rectangular, distinctly narrower than elytra (Fig. 12a); elytra at suture about as long as pronotum along midline, posterior margins broadly arcuate (Fig. 12a); abdomen broad, at base as wide as elytra or nearly so (Fig. 12a); integument strongly glossy, microsculpture of forebody with hexagonal sculpticells, pubescence sparse (Fig. 12a); head strongly narrowed basally behind eyes, and narrowly produced in front of eyes, eyes large and protruding, longer than genae (Fig. 12a); antennomeres I–III strongly elongate, IV–VI subquadrate to slightly transverse, VII–X moderately to strongly transverse (Fig. 12a). Male. Tergite VIII with 4 teeth, two lateral larger and two median ones smaller and in close proximity (Fig. 12c); sternite VIII parabolic apically (Fig. 12d); median lobe of aedeagus distinct, in lateral view bulbus broadly oval and slightly compressed dorso-ventrad, crista apicalis broad, of triangular shape, tubus short with apex broadly triangular and produced ventrad, its margins slightly sinuate (Fig. 12b). Female. Tergite VIII truncate apically (Fig. 12e); sternite VIII rounded apically (Fig. 1f); spermatheca S-curved, capsule pitcher-shaped, median invagination shallow; stem sinuate, swollen posteriorly (Fig. 12g). Distribution. Nearctic. Canada: ON. USA: ME, NH. Collection and Habitat data. Adults were captured by flight intercept traps on the floating Sphagnum mat of a kettle bog, and by window traps on the bog margin; also, on aquatic vegetation and in ON specimens were found in Carex and moss on logs in a pond. Collected primarily from May to September in NH, ME, and ON.
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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 | 0.001 |
| Meta-epidemiology (narrow) | 0.001 | 0.001 |
| Meta-epidemiology (broad) | 0.001 | 0.000 |
| Bibliometrics | 0.003 | 0.003 |
| Science and technology studies | 0.005 | 0.002 |
| Scholarly communication | 0.001 | 0.002 |
| Open science | 0.001 | 0.002 |
| Research integrity | 0.001 | 0.002 |
| Insufficient payload (model declined to judge) | 0.036 | 0.013 |
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".