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Enregistrement W6968691934 · doi:10.5281/zenodo.7052892

Kalanchoe robertsonii Gideon F. Sm. 2022, nothospec. nov.

2022· article· en· W6968691934 sur OpenAlexaboutno aff

Notice bibliographique

RevueZenodo (CERN European Organization for Nuclear Research) · 2022
Typearticle
Langueen
DomaineAgricultural and Biological Sciences
ThématiquePlant Diversity and Evolution
Établissements canadiensnon disponible
Organismes subventionnairesnon disponible
Mots-clésKalanchoeOrange (colour)InflorescenceTendrilCrassulaceae

Résumé

récupéré en direct d'OpenAlex

Kalanchoe × robertsonii Gideon F.Sm. nothospec. nov. (Fig. 2A–E). Type:— SOUTH AFRICA. Gauteng province —2528 (Pretoria): Tshwane, (– CA), ex hort., 25 April 2022, G. F. Smith 1180 (holotype PRU). Parentage:— Kalanchoe longiflora Schltr. ex Wood (1903: t. 320) × K. rotundifolia (Haworth 1824: 188) Haworth (1825: 31). Diagnosis:— Kalanchoe × robertsonii is a low-growing leaf succulent that in both vegetative and reproductive morphological characters is generally intermediate between its parents, K. longiflora and K. rotundifolia. However, leaves of K. × robertsonii are narrowly oblong to obovate rather than obovate to nearly orbicular as in K. longiflora or oblong-elliptic to elliptic-obovate as in K. rotundifolia. As in K. rotundifolia, the inflorescence of K. × robertsonii is a corymbose cyme, while that of K. longiflora is a thyrse. Kalanchoe × robertsonii has flowers that are gradually urnshaped above the ovary, but less so than in K. longiflora, while those of K. rotundifolia are abruptly urn-shaped above the ovary. Corolla tubes of K. × robertsonii are shiny greenish yellow, while those of K. rotundifolia are reddish orange and strongly green-infused proximally; those of K. × robertsonii are shiny light orange and lightly green-infused in the lower half. The colour of the adaxial surfaces of the corolla lobes of K. longiflora is monochromatic light yellow, that of K. rotundifolia is generally monochromatic red to dull orange, while that of K. × robertsonii is bicoloured, being dull to bright light orange distally and strongly yellow-infused proximally. Description:—Perennial, few- to many-leaved, sparsely branched from the base, glabrous, dull light green to glaucous, with light waxy bloom, small, low-growing succulent, with erect to leaning stems (0.25–)0.30–0.45(–0.50) m long when in flower. Stems few arising from fibrous rootstock, thin, erect to leaning, light glaucous green, strongly orange-infused to virtually orange throughout, simple at first, sometimes producing branchlets near the base, main stems with few branches higher up post-flowering, leafless lower down, especially at onset of dry season. Leaves (30–)45–60(–70) × (10–)14–18(–20) mm, glaucous to very light green, sometimes lightly or strongly orange-infused especially in dry season, with slight bloom, opposite-decussate, pseudo-rosulately clustered towards stem apices, very finely orange-dotted towards margins, generally sparsely arranged; petiole absent; blade succulent, narrowly oblong to obovate, flat, straight or slightly curved upwards; apex rounded, obtuse, blunt; base cuneate, gradually tapering towards stem; margin flat; entire for proximal ⅔–¾, usually with few rounded, harmless crenations towards leaf apex, often more intensely orange-infused. Inflorescence a corymbose cyme, (250–)270–300(–340) mm tall, with leaf-like bracts at nodes, floriferous only at the top, erect or leaning, apically sparsely branched, few- to many-flowered, rather round in outline when viewed from above, branches opposite, subtended by small, persistent leaf-like bracts, leafy branchlets not produced in axils, axis light glaucous green, strongly orange-infused to virtually orange throughout, with slight bloom; pedicels slender, 4–8 mm long, orange-infused. Flowers tetramerous, sometimes pentamerous, 15–16 mm long, erect; calyx light shiny green, strongly orange-infused, more intensely so distally, lacking a slight bloom; sepals 4, 2.5–3.0 × 1.0– 1.5 mm, separate, basally fused for about 1 mm, deltoid-elongated-triangular, acute, hardly contrasting against basal part of corolla, apically straight; corolla 14–15 mm long, enlarged basally around carpels, abruptly attached to pedicel, not distinctly and tightly anti-clockwise-twisted apically after anthesis; corolla tube 13–14 mm long, orange in bud, distally bright orange, greenish-infused around ovaries at anthesis, and basally at level of sepals, gradually becoming terete upwards above carpels, rounded-4-angled, gradually urceolate, somewhat box-shaped-square when viewed from below; lobes 4–5 × 3.5–4.0 mm, spreading at 90°-angle or slightly to distinctly recurved, bicoloured, dull to bright light orange distally, strongly yellow-infused proximally, ovate to very slightly elliptic; centrally shallowly furrowed, straight along margin, distinctly acute apically, minutely apiculate, not showing diurnal movement. Stamens inserted in two ranks just below and at middle of corolla tube, included but visible at mouth; filaments 2.0– 2.5 mm long, thin, yellow; anthers 0.75–1.00 mm long, dull yellow. Pistil consisting of 4 carpels; carpels 5–6 mm long, light green, strongly orange-infused; styles 2 mm long, yellowish green; stigmas whitish, prominently capitate; scales 2.00– 2.25 mm long, cylindrical to ribbon-like-linear, tapering upwards, light yellow. Follicles 7–8 mm long, light green, at first enveloped in dry, orange-brown, remains of corolla tube, often shedding dry corolla tube early on, then exposing still light green follicles, remains of corolla tube later turning whitish to brownish black, eventually brittle, grass spikelet-like, splitting star-like. Seed 0.4–0.5 mm long, brown to blackish brown, faintly striated, ellipsoid to somewhat banana-shaped-curved. Chromosome number: unknown. Flowering time:— Kalanchoe ×robertsonii flowers mainly in the autumn and winter months, (March–)April to July(–August), in the southern hemisphere. However it has been observed as flowering out-of-season in late-spring and in early-summer. Eponymy:— Kalanchoe × robertsonii is named for Prof. Dr Bruce Leonard Robertson (18 April 1944 [Pretoria, South Africa]–) (Fig. 2F) who, at the age of 17 enrolled at the University of Pretoria, graduating with an M.Sc. (Agriculture) for his study of the embryology of avocado [Persea americana Miller (1768: fifth page headed PER PER, page not numbered)] in 1969. In 1972 he joined the staff of the Department of Botany at the University of Port Elizabeth (U.P.E.), now the Nelson Mandela University, as a lecturer, where he obtained a Ph.D. in 1975 for his research on the distribution, seed germination, developmental anatomy, and embryology of the South African endemic palm, Jubaeopsis caffra Beccari (1914: 173) (see Wicht 1969: 35–37, Robertson 1976a, b, Jones 1995: 234–235, and Dransfield et al. 2008: 401–404). Bruce subsequently completed a postdoctoral sabbatical at the University of Alberta in Edmonton, Canada, where he researched the ultrastructural embryology of barley [Hordeum vulgare Linnaeus (1753: 84)]. Thereafter he returned to U.P.E. where he progressed through the academic ranks to Professor of Botany in 1991. In 1998 he was appointed as Director of the Institute for Coastal Research of U.P.E. His research during this period focussed mainly on the reproduction, harvesting, and aquaculture of macroalgae, leading to him undertaking projects at Dalhousie University, Halifax, Canada, as well as at the Marine Research Station in Tainan, Taiwan. His research programme produced a large number of research publications, and Master’s and Doctoral students. He was appointed Head of U.P.E.’s Department of Botany in 1998, and in 1999 he was appointed as the University’s first Director of Research. Professor Robertson occupied this post until his retirement in December 2004. As an emeritus Professor, he has continued to undertake contractual projects relating to research management and post-graduate student mentoring in a number of the University’s faculties. Professor Robertson served on and chaired numerous professional Boards and Councils, for example of the South African Association of Botanists, Phycological Society of South Africa, South African Council of Natural Scientists, South African Network for Oceanographic Research, and as the Senate Representative on the Council of the University of Port Elizabeth (2002–2004). The naming of K. × robertsonii for Prof. Robertson celebrates his 78 th birthday on 18 April 2022 and recognises his many and varied contributions to plant sciences in South Africa, and beyond.

Récupéré en direct depuis OpenAlex et désinversé. Les résumés ne sont pas conservés dans cette base de données : les index inversés représentent 8,6 Go des 9,3 Go de texte de la base, et le serveur dispose de 13 Go libres.

Comment cette classification a été obtenuedéplier

Prédiction machine sur la base complète

Imitation des enseignants

Ni prévalence calibrée, ni vérité terrain. Validation humaine à venir. Le volet Gemma est une étiquette directe du modèle pour chaque travail de la base, lue sur la notice réduite au titre. Le volet Codex est un classifieur appris des 10 348 étiquettes directes de Codex et calibré sur les taux pondérés de l'échantillon; les champs sans appui suffisant ne portent aucun appel Codex. Le mode candidate est l'union des deux volets; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont pas des étiquettes humaines.

score de la tête « metaresearch » (Codex)0,000
score de la tête « metaresearch » (Gemma)0,001
Version: metacan-v3-hybrid-931329e0061cStatut de validation: machine_predicted_unvalidated
Catégories candidatesaucune
Catégories consensuellesaucune
DomaineSignal candidat: aucune · Signal consensuel: aucune
Devis d'étudeSignal candidat: Observationnel · Signal consensuel: aucune
GenreSignal candidat: Empirique · Signal consensuel: aucune
Score de désaccord entre enseignants0,019
Score d'incertitude au seuil0,063

Scores du classifieur distillé par catégorie (deux têtes)

CatégorieCodexGemma
Métarecherche0,0000,001
Méta-épidémiologie (sens strict)0,0010,000
Méta-épidémiologie (sens large)0,0000,000
Bibliométrie0,0010,001
Études des sciences et des technologies0,0010,000
Communication savante0,0010,002
Science ouverte0,0010,001
Intégrité de la recherche0,0010,001
Charge utile insuffisante (le modèle a refusé de juger)0,0190,011

Scores machine (provisoires)

Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.

Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.

Tête enseignante Opus0,027
Tête enseignante GPT0,186
Écart entre enseignants0,159 · la distance entre les deux têtes enseignantes sur ce seul travail
Statut de validationscore_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découle

Classification

machine, non validée

Prédiction automatique; un appel candidat d’une seule source (Gemma direct ou Codex distillé), pas un consensus.

Les modèles n’ont appliqué aucune catégorie : rien dans la taxonomie ne correspondait à ce travail.
Devis d'étudeObservationnel
Domainenon disponible
GenreEmpirique

Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».

En bref

Citations0
Publié2022
Routes d'admission1
Résumé présentoui

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