Bibliographic record
Abstract
Bolshecapnia spenceri (Ricker, 1965) http://lsid.speciesfile.org/urn:lsid: Plecoptera.speciesfile.org: TaxonName:5022 (Figs. 25-34) Capnia (Bolshecapnia) spenceri Ricker, 1965:481. Holotype ♂ (Canadian National Collection), Consolation Lake, Banff National Park, Alberta Bolshecapnia spenceri: Ricker & Scudder, 1975:338 Distribution. CANADA: AB, BC, UNITED STATES: MT (DeWalt et al. 2018) Material examined. CANADA: Alberta: Consolation Lake, near Moraine Lake, Banff National Park, 51.316 N, - 121.77 W, 1 June 1958, W.E. Ricker, Holotype ♂, Allotype ♀, 37 Paratypes (CNC). Same data, 2♂, 1♀ (INHS, Paratypes). British Columbia: Headquarters Creek near Sorcerer Glacier, Selkirk Mountains, 14 July 1960, J. Ricker, 3♀ Paratypes (CNC). NW branch Lyell Creek, Golden, 30 June 1961, J. Ricker, 1♀ Paratype (CNC). UNITED STATES: Montana: Glacier Co., Iceberg Lake, Glacier National Park, 3 July 1968, S.M. Stauffer, 4♂ (USNM). Same site, 5 July 1981, Levine, Weber, 7♂, 2♀ (FLBS). Same site, 5 July 1981, W.D. Shepard, 26♂, 1♀, 2 larvae (CAS). Same site, 17 July 1971, G.G. Lawley, 1♂ (BYU). Same site, 20 July 1966, P. Milam, 11♂ (FLBS). Same site, 21 July 1979, B. Stark, K.W. Stewart, R.W. Baumann, 97♂, 48♀, 32 larvae (BPSC, BYU). Same site, 24 July 1964, D. C. Lowrie, 18♂, 2♀ (BYU). Same site, 28 July 1970, R.A. Haick, 1♂, 1♀ (BYU). Same site, 29 July 1969, R.A. Haick, 94♂, 20♀ (BYU, USNM). Same site 29 July 1970, R.A. Haick. 2♂, 2♀ (USNM). Same site, 5 August 1972, R.A. Haick, 87♂, 22♀ (USNM). Iceberg Lake, above trail to lower lake, 48.81944 N, - 113.76401 W, 15 July 2013, J. Giersch, 1♀ (USGSAIC). Iceberg Creek, below Iceberg Lake, Glacier National Park, 28 July 1964, A. R. Gaufin, 1♀ (BYU). Same site, 48.82098 N, - 113.73896 W, 14 July 2014, J. Giersch, 3♀ (USGSAIC). Iceberg Lake, Glacier National Park, 5 mi NW Many Glacier Hotel, 28 July 1964, A. R. Gaufin, A.V. Nebeker, 36♂, 6♀ (CNC). Iceberg Lake, Glacier National Park, Many Glacier Campground Area, 29 July 1969, A. R. Gaufin, 91♂, 20♀ (BYU). Sue Lake, east shore, Glacier National Park, 48.861896 N, - 113.84058 W, 8 August 2012, J. Giersch, 6♀ (USGSAIC). Tarn above Preston Park, Glacier National Park, 48.72157 N, - 113.63796 W, 27 July 1997, J. Giersch, 2♂, 1♀ (USGSAIC). Upper Twin Lakes Basin, Proglacial pond outlet, NW Fusillade Mountain, Glacier National Park, 48.64387 N, - 113.73931 W, 22 September 2015, J. Giersch, 1 larva (USGSAIC). Male epiproct (n = 6). Length 524-543 μm, width at midlength 224-250 μm, greatest width near base 295-300 μm. Sclerotized hooks arise subapically from either side of the median groove, and are bent sharply laterad, and extend beyond the lateral margins of the epiproct body (Figs. 25-29); tips of basolateral hooks extend forward for about 0.75 of the total epiproct length. Median groove wide near apex, narrowing gradually to the widest point near the epiproct base (Fig. 26). Small clumps of spongy appearing tissue located along lateral margins near base of hooks (Figs. 27-28). Base of epiproct body bearing a pair of dorsal ridges separated by terminus of median groove (Figs. 27, 29). Apex with a protruding membranous process (Figs. 29- 30). Tergal process (n = 3). Absent, but tergum 9 covered with a broad band of short, thick setae (Figs. 27-28). Vesicle (n = 1). Length = 219 μm, basal width =. 214 μm, median width = 252 μm. Process relatively wide, slightly wider near midlength (Fig. 31-32). Ventral surface covered with thick setae. Female subgenital plate (n = 3). This structure is an apically narrowed, tongue-shaped process, about twice as wide at midlength as near the apical margin (Figs. 33-34); the structure extends beyond the anterior margin of sternum 9 (see fig. 169 in Baumann et al. 1977), and is hairless except for a few scattered long setae on the basal half. Several variations in the structure are shown in figs. 15-16 (Ricker 1965). Larva. Described by Stewart & Stark (1988, 2002) and Stewart & Oswood (2006). The larval characteristics listed above for the genus are based on these descriptions.
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 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) | 0.001 | 0.000 |
| Meta-epidemiology (broad) | 0.000 | 0.000 |
| Bibliometrics | 0.003 | 0.002 |
| Science and technology studies | 0.003 | 0.001 |
| Scholarly communication | 0.001 | 0.001 |
| Open science | 0.001 | 0.001 |
| Research integrity | 0.001 | 0.001 |
| Insufficient payload (model declined to judge) | 0.030 | 0.010 |
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.
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".