Diploneis disjuncta Jovanovska & Wilson & Hamilton & Stone 2023, sp. nov.
Bibliographic record
Abstract
Diploneis disjuncta sp. nov. (LM Figs 214–248, SEM Figs 249–257) Valves are weakly asymmetric, linear-elliptic with weakly convex margins and round apices (Figs 214–250). Valve length is 17.5–32.5 μm and valve width is 9–13.5 μm. The axial area is very narrow, linear to lanceolate, slightly widening into a small to indistinguishable and weakly asymmetric central area (Figs 214, 250, 253), 1.8–3 μm wide. Externally, the canal is linear to lanceolate, slightly expanded in the middle of the valve with three to two rows of cribrate (<15 poroids) areolae narrowing into one at the valve apices (Figs 249, 250, 251, 253). Internally, a thick non-porous slightly raised silica plate encloses the longitudinal canal (Figs 254, 255). Externally, the raphe is filiform, curved with expanded proximal ends deflected to one side; the proximal raphe ends are positioned within a linear expanded depression (Figs 250, 253). The distal raphe ends are unilaterally bent to the same side and terminate on the valve face (Figs 249, 251). Internally, the raphe is curved with simple proximal and distal ends that are slightly elevated in a depression formed by the longitudinal canal (Figs 254–257). The striae are parallel at mid-valve becoming radiate towards the apices, 11–12 in 10 μm. Striae are uniseriate at the center of the valve (white arrow in Fig. 250) and biseriate at the apices (black arrow in Fig. 250). The striae are composed of round areolae externally covered with fine pored cribra (25 poroids), 20 in 10 μm. The inter-areolar thickenings have fin-like silica ridges (mostly absent and hardly visible on the illustrated specimens probably as a result of corrosion, Figs 250, 253). The areolae increase in size towards the valve margins (Fig. 252). Internally, the alveoli open via a single elongated opening covered with a thin silica layer (Figs 254, 256, 257). The valvocopula has serrated advalvar edges (Fig. 255). Type:— REPUBLIC OF ZAMBIA, Lake Tanganyika, Cape Nandu, Kasaba Bay, at 768 m elevation; sand and mud, 20 m water depth, collected with Van Veen grab sampler, 8°30’18.9” S 30°38’32.3” E, E. Jovanovska, 2 nd October 2021 (holotype designated here, circled specimen BM-108992! = Fig. 224, isotypes ANSP-GC17221!, CANA-129326!). Type material CANA-129326. Registration: http://phycobank.org/103703 Pictures of the isolated specimen:— LM micrograph on 1000× magnification (Fig. S3y). Sequence data:— Plastid gene rbc L sequence (GenBank accession: OQ 660294). Etymology:— The specific epithet ‘ disjuncta ’ refers to the disjunct distribution of uniseriate and biseriate striae. Ecology and distribution:— Diploneis disjuncta sp. nov. has only been observed along the Tanzanian and Zambian coasts in the southern and central sub-basins of Lake Tanganyika. This relatively small species is quite common in the alkaline, moderately mineral-rich and highly transparent waters on the sand and mud surface (sometimes interspersed with mollusk shells) between 15 and 33 m water depth, especially in Mahale National Park, but also in Isanga Bay, Chituta Bay, and Mutondwe Island (Fig. 1 c, e, f). At all sites, the species occurs together with D. decora sp. nov., D. serrulata sp. nov., D. kilhamiana sp. nov., D. cocquytiana sp. nov., D. duplex sp. nov., D. salzburgeri sp. nov., D. clara sp. nov., D. fossa sp. nov., and D. tanganyikae sp. nov. Main differential characters:— Valve size, striae pattern, narrow canals, external fin-like ornamentations across the valve, and poroids ca. 25 per areola. Similar species:— Diploneis duplex sp. nov. and Diploneis mineroviciae Lange-Bertalot, Fuhrmann & Werum (2020: 80).
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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 | 0.000 |
| Meta-epidemiology (broad) | 0.000 | 0.000 |
| Bibliometrics | 0.001 | 0.001 |
| Science and technology studies | 0.001 | 0.001 |
| Scholarly communication | 0.001 | 0.001 |
| Open science | 0.000 | 0.001 |
| Research integrity | 0.001 | 0.001 |
| Insufficient payload (model declined to judge) | 0.005 | 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".