Parasyrisca bucklei Marusik & Fomichev, 2010, sp. n.
Bibliographic record
Abstract
Parasyrisca bucklei sp. n. Figs 1–6, 9–15 Etymology. The specific name is a patronym in honour of our colleague Donald J. Buckle (Saskatoon, Canada). Material. RUSSIA: Holotype 3 and paratypes 5Ƥ (SZMN) Altai, Kuraisky Mt. Range, 50º20’N, 87º44’E, mountain stony tundra, 2800–3000 m, 5.07.2009 (A.Fomichev). 13 3Ƥ 1 juv. (ZMMU), same locality, 11– 12.07.2007 (P.Y.Ustyuzhanin). Diagnosis. The new species is closely related to two Siberian species, P. logunovi Ovtsharenko, et al., 1995 and P. belengish Ovtsharenko et al., 1995 (see Ovtsharenko et al., 1995: figs 62–66, 75–76). It can easily be distinguished from the former species by the shape of its conductor with an extended terminal part (conductor with parallel lateral borders in P. logunovi) and the spermatheca terminating over the anterior hood. It can be separated from P. belengish by a more elongate terminal part of the spermathecae. Description. Male. Total length 9.2–10. Carapace: 3.8–4.6 long, 3.2–3.6 wide. Cymbium 1.7–1.8 long. Body light brown without pattern. Palp as in Figs. 1–6. Tibial apophysis with five teeth (Fig. 6), embolus flat, partly exposed (Figs 1, 4), conductor with extended terminal part. Leg article length of male with carapace 3.8 long and in female with carapace 5.3 long. Femur Patella Tibia Metatarsus Tarsus Female. Total length 9.5–14. Carapace: 3.8–5.3 long, 3.2–4.1 wide. Colouration as in male. Epigyne (specimens with carapace 5.3 long) – 1.0 high and 0.9 wide. Epigyne as in Figs 9–15. Shape is variable, anterior hood small, posterior hood about three times wider, posterior part distinctly subdivided, lateral sides of fovea in most specimens almost parallel. Spermathecae with parallel sides, head of spermathecae elongate. Comments. This species, like most species known from numerous females, demonstrates a rather strong variation in the shape of epigyne (Figs. 9–15). Distribution. Only the type locality. Figures 17–18. Photograph showing the habitat in which Parasyrisca bucklei sp. n. was collected (17) and map showing type locality (18).
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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) | 0.001 | 0.000 |
| Meta-epidemiology (broad) | 0.000 | 0.000 |
| Bibliometrics | 0.002 | 0.001 |
| Science and technology studies | 0.002 | 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) | 0.013 | 0.006 |
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".