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Record W6950693416 · doi:10.5281/zenodo.5764133

Marsdenia mayottae W. D. Stevens, Labat & Barthelat 2016, spec. nova

2016· article· en· W6950693416 on OpenAlex

Why this work is in the frame

A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.

affAt least one author lists a Canadian institution in the pinned OpenAlex snapshot.

Bibliographic record

VenueZenodo (CERN European Organization for Nuclear Research) · 2016
Typearticle
Languageen
FieldMaterials Science
TopicPhytochemistry and Bioactive Compounds
Canadian institutionsMinistère des Ressources naturelles et des Forêts (Québec)
Fundersnot available
KeywordsPedicelApex (geometry)CalyxBractPetiole (insect anatomy)

Abstract

fetched live from OpenAlex

Marsdenia mayottae W.D. Stevens, Labat & Barthelat, spec. nova (Fig. 1, 2). Typus: M AYOTTE: Grande Terre, Bandré, Rassi Abambo, 9.II.2001, Barthelat, M’Changama & Ali Sifari 295 (holo: P [P00229277]!; iso: G!, K!, MAO!, MO!, P [P00282507]!). Marsdenia mayottae W.D. Stevens, Labat & Barthelat is most similar to M. vohiborensis Choux, but differs from this species by its umbonate style apex completely covered by the terminal anther appendages and the absence or near absence of a corona. Shrub or twining vine, woody but apparently not corky, underground parts unknown, stems densely appressedpuberulent, sparsely lenticellate, internodes 1-6 cm; latex white. Leaves opposite; blades 6.5-11.1 × 4-9.2 cm, ovate to elliptic, glabrous or puberulent on veins below; apex acuminate to attenuate; base truncate to shallowly lobate, its sinus up to 5 mm deep, lateral veins 4 to 6, colleters 10 to 24; petiole 2.4-5.5 cm, sparsely puberulent. Inflorescences solitary, paniculate with 2 to 6 congested-racemose, appressedpuberulent branches; peduncle (3) 10-48 mm; fertile axes up to 3 cm long, more or less covered with pedicel scars. Flowers borne on pedicels 4–9 mm long; bracts numerous and conspicuous, 1.5-10 × 0.6-4 mm, elliptic to spathulate, sometimes leaf-like; calyx with 1 colleter below each sinus within, lobes elliptic to ovate with round tips, unequal, 3-4 × 1.7-2 mm, sparsely puberulent along axis abaxially, not ciliolate, green; corolla shallowly campanulate, dull yellow, without calli, barbate in distal half of tube and proximal half or more of each lobe adaxially, glabrous abaxially, tube 1.7-2.3 mm, lobes elliptic with tip rounded, 2.2-3 × 1.6- 1.7 mm, patent; corona lobes absent or if present reduced to a fleshy tooth adnate to base of anther, deltate, up to 0.4 mm long, 0.2 mm wide at base; gynostegium nearly sessile, guide rails 0.7 mm long, slightly salient at base; anthers trapezoidal, nearly rectangular, 0.8-1 × 0.8-1 mm, terminal appendages 0.6 × 0.6 mm, elliptic to ovate, translucent, corpusculum ellipsoid to subsagittoid, 0.19-0.28 × 0.08-0.13 mm, translators flat, 0.19-0.25 × ca. 0.05 mm, pollinia ellipsoid to obovoid, 0.39-0.43 × 0.24-0.3 mm; style apex umbonate, 1.4-1.5 mm wide at base. Follicles narrowly ovoid with asymmetrical base, 7.5-9.5 × 2.5-3.5 cm, smooth, glabrous, follicle wall 5-7 mm thick; seeds elliptic, 8-11 × 5-7 mm, dark grey-brown with red-brown mottling, margin 0.6-0.7 mm wide, distally entire or inconspicuously crenulate, surface smooth, coma 3.5-4 cm long, white. Distribution, habitat and phenology. – Marsdenia mayottae is only known from Mayotte, where it can be found at low elevations (less than 10 m a.s.l.) in littoral forest growing with Thespesia populnea (L.) Sol. ex Corrêa, Xylocarpus granatum Koenig, Mimusops comorensis Engl., Maytenus undata (Thunb.) Blakelock and Calophyllum inophyllum L. It is also found on coastal squeletic soils on basaltic rock or in dry littoral scrubland with Grewia picta Baill., G. triflora (Bojer) Walp., Guettarda speciosa L. and Maytenus undata. In addition, it can be found also on calcareous sand soil with Talipariti tiliaceum (L.) Fryxell. The new species is very rarely present also in dry lowland forest on other substrates at up to 100 m. Marsdenia mayottae has been recorded in flower from November to January and in fruit in May and June. Vernacular names and local use. – The following vernacular names in Shibushi have been recorded for M. mayottae by Barthelat & Boullet (2005) or on herbarium labels: “Pamba suisui be” or “Pamba suisui famakitrano”, “Macarangana vahi”, “Vahy rotono”, “Vahy maro” and “Kidoro voalavo”. The plants are used in the preparation of magic potions known as “grigris” (M. M’changama, pers. comm.). Conservation status. – Marsdenia mayottae is only known from highly threatened littoral and lowland dry forests on Mayotte, and its population, as currently known, is highly fragmented. It is only known from five locations despite intensive inventories in the last decades. Thus, its preliminary risk of extinction can be assessed as “Endangered” [EN B2ab(iii)] following the IUCN Red List Categories and Criteria (IUCN, 2012). Notes. – This species shares a dense, bracteate inflorescence with M. vohiborensis Choux from the central plateau of Madagascar. However, M. vohiborensis has a long-exserted style apex while M. mayottae has an umbonate style apex completely covered by the terminal anther appendages. The absence or near absence of a corona in M. mayottae is unique among the species of Marsdenia of Madagascar and the Comoros, and rare in the genus. Paratypi. – M AYOTTE: Grande Terre, Saziley, 17.I.2001, Barthelat & Ali Sifari 233 (G, K, MAO, MO, P); Petite Terre, Labattoir, Plage de Moya, 15.I.2002, Barthelat & Ali Sifari 694 (K, MAO, MO, P); ibid. loc., 15.I.2002, Barthelat & Ali Sifari 699 (MAO, MO, P); Grande Terre, Mliha, Mtsumbatsu, 20.XII.2001, Barthelat et al. 625 (MAO, MO, P); sommet du Bouzi, X.1850, Boivin s.n. (P); Rassi Maoussi, 17.V.1999, Mas 176 (P); Sohoa, 28.VI.1997, Pascal 942 (G, MO, P).

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.

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesInsufficient payload (model declined to judge)
Consensus categoriesInsufficient payload (model declined to judge)
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.613
Threshold uncertainty score0.955

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0010.000
Scholarly communication0.0000.000
Open science0.0010.001
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0770.045

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.

Opus teacher head0.036
GPT teacher head0.247
Teacher spread0.211 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it