Diploneis tenera Jovanovska & Wilson & Hamilton & Stone 2023, sp. nov.
Bibliographic record
Abstract
Diploneis tenera sp. nov. (LM Figs 152–171, SEM Figs 172–177) Valves are asymmetric, linear-elliptic with parallel to weakly convex margins and round apices (Figs 152–172). Valve length is 29–47.5 μm and valve width is 14.5–20 μm. The axial area is linear to lanceolate, widening at the center to form a longitudinally elongate and weakly asymmetric central area (Figs 153, 172), 2.5–4 μm wide. Externally, the canal is linear to lanceolate, slightly expanded in the middle of the valve with three rows of cribrate areolae narrowing into one at the valve apices (Figs 152–172). Internally, a thick non-porous slightly raised silica plate encloses the longitudinal canal (Fig. 174). Externally, the raphe is filiform, curved with expanded proximal ends deflected to one side; the proximal ends are positioned within tear drop depressions (Fig. 172). The distal raphe ends are unilaterally bent to the same side and terminate at the valve face mantle junction (Figs 172, 173). Internally, the raphe is curved with simple proximal and distal ends that are slightly elevated in a depression formed by the longitudinal canal (Figs 174, 175, 177). The striae are parallel at mid-valve changing to radiate towards the valve apices, 10–11 in 10 μm. Striae are uniseriate becoming biseriate towards the valve margins (Figs 173, 175). The striae are composed of round to rectangular areolae covered externally with a dense cribra (>15 poroids), 15–20 in 10 μm. The inter-areolar thickenings have fin-like crest shaped silica ornamentations serrated into ca. 3–5 notched edges (Fig. 173). The fin-like ornamentations around the canal are bent into semi-circular shapes, positioned towards the striae whereas those of the striae are only slightly bent and positioned towards the canal, changing opposite direction only at valve mantle (Figs 172, 173). The areolae increase in size towards the valve margins (Fig. 173). Internally, the alveoli open via a single elongated opening covered with a thin silica layer (Fig. 176). The valvocopula has serrated advalvar edges (Figs 174, 176). Type:— REPUBLIC OF ZAMBIA, Lake Tanganyika, Kalambo Falls Lodge, at 782 m elevation; sand from fish crater, 7.5 m water depth, collected SCUBA diving, 8°37’22.9” S 31°12’01.8” E, W. Salzburger, 29 th September 2021 (holotype designated here, circled specimen BM-108981! = Fig. 157, isotypes ANSP-GC17210!, CANA-130009!). Type material CANA-129325. Registration: http://phycobank.org/103719 Pictures of the isolated specimen:— LM micrograph on 1000× magnification (Fig. S3q). Sequence data:— Plastid gene rbc L sequence (GenBank accession: OQ 660297). Etymology:— The specific epithet ‘ tenera ’ refers to structurally simple valves and valve ornamentations. Ecology and distribution:— Diploneis tenera sp. nov. has only been observed along the Zambian and Tanzanian coasts of Lake Tanganyika. In the alkaline, moderately mineral-rich and highly transparent waters, the species occurs mainly in sandy substrates (sometimes with mollusk shells) and rarely in submerged rocks between 15 and 20 m water depth in the southern sub-basin at Kalambo Falls Lodge, Isanga Bay, Mutondwe Island, and Cape Nangu in Kasaba Bay, and less so in the central sub-basin in Mahale National Park (see Fig. 1c, e, f). It is quite abundant especially at Kalambo Falls Lodge and in Kasaba Bay where it occurs together with D. kilhamiana sp. nov., D. gigantea sp. nov., D. decora sp. nov., D. serrulata sp. nov., D. salzburgeri sp. nov., D. duplex sp. nov., and D. clara sp. nov. Main differential characters:— Valve shape, striae pattern, external thick fin-like ornamentations across the valve, and poroids 15–20 per areola. Similar species:— Diploneis tessellata sp. nov. and Diploneis rumrichorum Lange-Bertalot & Fuhrmann (2020: 121).
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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 | 0.002 | 0.001 |
| Science and technology studies | 0.001 | 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) | 0.006 | 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".