Research Article |
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Corresponding author: Bonaventure Sonké ( bonaventure.sonke@ird.fr ) Academic editor: Elmar Robbrecht
© 2026 Bonaventure Sonké, Murielle Simo-Droissart, Ehoarn Bidault, Fernandez Ngoula, Olivier Lachenaud.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Sonké B, Simo-Droissart M, Bidault E, Ngoula F, Lachenaud O (2026) Nectaropetalum camerunense (Erythroxylaceae), a new species from the Sanaga basin in Cameroon, with a key to the genus. Plant Ecology and Evolution 159(3): 461-469. https://doi.org/10.5091/plecevo.190713
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Background and aims – This paper describes and illustrates a new species of Nectaropetalum (Erythroxylaceae) from the Sanaga River basin in Cameroon. The genus otherwise includes eight species: two in the Democratic Republic of the Congo, five in coastal areas of eastern and southern Africa, and one in Madagascar.
Material and methods – The description of the new species is based on the study of 13 gatherings, field observations, and a comparison with available material of its congeners in BR and K. Its conservation status was assessed following the IUCN Red List Categories and Criteria.
Key results – The discovery is an important westwards range extension for the genus. Nectaropetalum camerunense sp. nov. most closely resembles N. acuminatum from Tanzania in vegetative characters, but differs by its shorter sepals and short thickened pedicels (vs sessile flowers). A key to the genus Nectaropetalum is presented. The new species is endemic to the middle Sanaga basin in Cameroon, where it occurs gregariously in periodically flooded riverine forests. It is assessed as Endangered following IUCN Red List Categories and Criteria. This brings the total number of Sanaga basin riverine endemics to date to nine, all of which are currently facing significant threats from agriculture and the construction of hydroelectric dams.
Central Africa, conservation, IUCN Red List assessment, riverine forests, taxonomy, threatened species
Cameroon’s forests are among the most biologically diverse in tropical Africa (
In 2021, a team of scientists from Institut de Recherche pour le Développement (IRD, France), the Plant Systematics and Ecology Laboratory (University of Yaoundé I), Biotope (an environmental consultancy based in France), and the Missouri Botanical Garden initiated an Environmental and Social Impact Assessment (ESIA) for a hydro-electric project at Kikot, along the Sanaga River. This study identified several taxonomic novelties, including the recently described Drypetes stevartii Sonké & Quintanar (Putranjivaceae;
Erythroxylaceae are a pantropical family, comprising ca 270 species in four genera (
Key morphological characters and distribution of genera in Erythroxylaceae. Characters particular to one genus are highlighted in bold.
| Aneulophus | Erythroxylum | Nectaropetalum | Pinacopodium | |
| Leaves | opposite | alternate | alternate | alternate |
| Stipules | interpetiolar, caducous | intrapetiolar, persistent (rarely caducous) | intrapetiolar, caducous | intrapetiolar, caducous |
| Inflorescences | fasciculate | fasciculate (or 1-flowered) | fasciculate (or 1-flowered) | cymose |
| Inner scale of petals | absent | well-developed, exceeding the sepals | present but reduced, often hidden by the sepals (rarely absent) | present but reduced, hidden by the sepals |
| Ovary | 3(–4)-locular | (2–)3-locular | 2-locular | 2-locular |
| Styles | 3(–4), free | (2–)3, free or connate at base | 1, bilobed | 1, bilobed |
| Fruits | capsular, 3-valved | drupaceous | drupaceous | ? (mature fruits not known) |
| Distribution | Central Africa | pantropical | Central, Eastern & Southern Africa, Madagascar | Central Africa |
Nectaropetalum was originally classified in Linaceae (
Apart from the relatively frequent East African N. kaessneri, most Nectaropetalum species are uncommon and rarely collected. None has yet been recorded from the Atlantic side of the African continent (e.g.
The description of the new species, as well as information about its distribution, habitat, and phenology, is based on field work conducted in Cameroon and on the study of 13 herbarium gatherings (including spirit material), all of which were made by the authors and deposited in the following herbaria: BR, BRLU, K, M, MA, MO, P, WAG, and YA (herbarium codes according to
Note: As suggested by
| 1. | Sepals imbricate, their margins widely overlapping; Madagascar | Nectaropetalum eligulatum |
| – | Sepals valvate, or sometimes very slightly imbricate in bud; continental Africa | 2 |
| 2. | Leaves obtuse to emarginate at apex; petals 7–28 mm long | 3 |
| – | Leaves acuminate at apex; petals 2.5–12 mm long | 4 |
| 3. | Flowers borne in leaf axils or just below the leaves; petals 7–19 mm long; Somalia to Tanzania | N. kaessneri |
| – | Flowers borne at leafless nodes; petals 20–28 mm long; Mozambique | N. carvalhoi |
| 4. | Stipules 10–23 mm long, leaving annular scars; flowers sessile or very shortly (≤ 1 mm long) pedicellate; South Africa | N. capense |
| – | Stipules ≤ 8 mm long, leaving interrupted scars; flowers sessile or with pedicel up to 10 mm long | 5 |
| 5. | Stipules bifid for around 1/3 of their length, leaving scars about half as wide as the twig; petals 2.5–4 mm long, with internal scale reaching around 1/3 of their length; D.R.Congo | N. lebrunii |
| – | Stipules not or very shortly bifid, leaving scars almost as wide as the twig (with only a narrow interruption on the side opposite the petiole); petals 6–12 mm long, with internal scale much shorter | 6 |
| 6. | Flowers and fruits on slender pedicels 5–10 mm long | 7 |
| – | Flowers and fruits sessile or with short and thick pedicels up to 1 mm long | 8 |
| 7. | Leaf secondary veins strongly curved and distinctly more prominent than tertiary veins; young flower buds (still enclosed in the calyx) markedly 5-angled; D.R.Congo | N. evrardii |
| – | Leaf secondary veins almost straight and hardly more prominent than tertiary veins; young flower buds (still enclosed in the calyx) almost circular in section; South Africa, Kenya, Tanzania | N. zuluense |
| 8. | Calyx lobes 2.2–2.5 mm long; flowers and fruits sessile; leaf blade 2.8–7 × 1–3 cm; Tanzania | N. acuminatum |
| – | Calyx lobes 1–1.5 mm long; flowers and fruits on short thick pedicel 0.5–1 mm long; leaf blade usually larger, 4–17 × 1.4–4.3 cm; Cameroon | N. camerunense |
CAMEROON • Central Region; Mbébé (Silobé); 4°07’45.41”N, 11°00’11.63”E; 28 Mar. 2025; fl.; Sonké & Ngoula 7959; holotype: BR [BR0000017787413]; isotypes: BR [BR0000017787406], BRLU [BRLU0045381, BRLU0045382, BRLU0045383], E, FR [FR-0038706], K, M, MA, MO, P, WAG, YA.
This species has acuminate leaves, and stipules leaving sub-annular scars with a narrow interruption on the side opposite the petiole, in which characters it resembles N. acuminatum Verdc.; it differs from the latter by its shorter calyx lobes, 1–1.5 mm long (vs 2.2–2.5 mm) and short thickened pedicels 0.5–1 mm long (vs pedicels absent).
Small tree or shrub up to 12 m tall, multi-stemmed; stems up to 12 cm in diameter. Twigs obliquely ascending, slightly flattened when young, then cylindrical, glabrous, soon covered with a pale grey-brown bark. Stipules 4.5–6.5 × 1–2 mm, intrapetiolar, narrowly triangular, folded lengthwise and initially forming a conical bud, entire or shortly (≤ 0.7 mm) bifid at apex and sometimes minutely fimbriate on the margins, with two dorsal keels, glabrous or with short sparse hairs on the keels, soon caducous and leaving sub-annular scars on the twigs (with an interruption on the side opposite the petiole). Leaves deciduous, appearing with the flowers, light green to burgundy when young, glabrous; petiole 4–6 mm long, 2-angled to slightly winged; blade 4–17 × 1.4–4.3 cm, oblong to elliptic, the base cuneate to obtuse, the apex gradually acuminate, thinly papyraceous, drying olive brown, or the lower side sometimes glaucous; midrib depressed on the upper side; secondary nerves 9–27 on each side, rather faint (only slightly more prominent than tertiary venation), forming irregular loops which anastomose 2–5 mm from the leaf margin; tertiary venation densely reticulate, forming areolae ca 0.5 mm in diameter, visible on both sides (both in fresh and dry state). Flowers axillary or sometimes borne at leafless nodes, solitary or in fascicles of up to 5, 5-merous, subtended by small, ovate to semi-circular bracts, 0.4–0.8 mm long, obtuse to rounded, fimbriate, persistent or caducous. Pedicel 0.5–1 mm long and thick, truncated-obconical, glabrous. Calyx lobes 5, almost free, 1–1.5 × 0.5–0.8 mm, triangular, acute, green, glabrous, valvate and completely enclosing the young bud. Petals 5, 8–10 × 2–3 mm, free, oblong, the apex rounded, white, glabrous, with a basal claw 1–1.5 mm long, and two internal scales, 0.3–0.8 mm long, triangular to semi-circular, borne just above the claw. Stamens 10, in a single whorl, the filaments alternately long (4–6 mm) and short (2.5–4 mm), united at base into a shallow cup 0.5–1 mm high, white; anthers 0.7–1.5 × 0.2–0.7 mm, oblong to elliptic, basifixed, dithecous, opening by longitudinal slits, brownish. Ovary 1.8–3 × 0.8–1 mm, 2–locular, with a single ovule per chamber, oblong, olive green, glabrous. Style 3–4.5 mm long, much longer than ovary, slightly shorter to slightly longer than stamens, linear, glabrous, the apex bilobed, the stigmas ca 0.5 mm long, elliptic, spreading to reflexed. Fruits 12–13 × 4–7 mm, fusiform to ovoid, the apex slightly beaked, yellowish green when fresh, grey-green after drying, with persistent calyx and stamens at base (the style sometimes persistent too). Seeds not seen.
Nectaropetalum camerunense is, based on current evidence, endemic to the middle Sanaga basin in Cameroon (Fig.
The species occurs in riverine forest, 320–420 m a.s.l., on the banks of the Sanaga River and its tributary the Lobo River. These forests have a relatively low canopy (15–20 m tall), and an open undergrowth mainly consisting of Thunbergia sp., Psychotria leptophylla Hiern, and Rinorea dentata (P.Beauv.) Kuntze. Nectaropetalum camerunense is gregarious in this habitat (Fig.
Nectaropetalum camerunense. A. Apex of twig with young leaves and intrapetiolar stipules. B. Same, with leaves seen from the lower side. C. Same, with leaves seen from the upper side. D. Flowers and young leaves (note unequal stamen filaments). E. Twig with flower buds, one open flower, and old flowers. F. Habit. A, F from Sonké & Ngoula 7961; B, from Sonké & Ngoula 7965; C, D, E from Sonké & Ngoula 7959. Photos by Bonaventure Sonké.
Nectaropetalum camerunense A. Twig with fruit and flower buds. B. Fruit (note style at apex and stamens persistent at base). C. Leafless twig with flower buds and one fruit. D. Multi-stemmed base of the tree. A from Sonké & Yemdji 8027; B, C from Sonké & Yemdji 8026; D from Sonké & Ngoula 7965. Photos by Bonaventure Sonké.
Flower buds appear in September, but the flowers open only in late March, at the start of the rainy season and when the leaves are sprouting. The flowering period is very short, lasting no more than two weeks. While most flowers in an inflorescence open at almost the same time, buds, open flowers, and withered flowers may occasionally be observed on the same branch (Fig.
The species name was chosen since it is endemic to Cameroon, and the only species of Nectaropetalum occurring in the country.
Nectaropetalum camerunense is known from 13 gatherings representing 12 unique occurrences and one or two subpopulations. Its extent of occurrence (EOO) is calculated as 35.6 km2, which falls within the limits of the Critically Endangered category under criterion B1. Its area of occupancy (AOO) is estimated as 12 km2, which falls within the limits for the Endangered category under criterion B2. Seven occurrences, which are located downstream of the Kikot hydroelectric dam project are threatened by shifting agriculture (one location). However, they are not expected to be affected by the dam project itself (not a regulating dam). No threats were identified to the four occurrences located at Ntol-Lébanga upstream of the dam project; these four occurrences represent one location. With regard to the most serious plausible threat, which is shifting agriculture, the 12 occurrences represent two locations, which falls within the limits of Endangered according to criterion B. We expect that shifting agriculture has led to a decline in habitat extent and quality and number of mature individuals, and will continue to do so in the future. For all these reasons, Nectaropetalum camerunense is assessed as Endangered: EN B1ab(iii,v)+2ab(iii,v).
This species most closely resembles N. acuminatum, which is still only known from its type, collected in Tanzania. Although their ranges are separated by a gap of over 3,000 km, the two species are highly similar, and differ mostly in the size of their calyx lobes and pedicel development; additional differences in the style and ovary (Table
Main morphological differences between Nectaropetalum acuminatum and N. camerunense.
| N. acuminatum | N. camerunense | |
| Leaf blade size | 2.8–7 × 1–3 cm | 4–13 × 1.4–4 cm |
| Number of flowers per axil | 1(2) | 1 to 5 |
| Pedicel | absent | short and thick, 0.5-1 mm |
| Calyx lobes (length) | 2.2–2.5 mm, acuminate | 1–1.5 mm, acute |
| Ovary | 3–5 mm long, narrowly cylindrical | 1.8–3 mm long, oblong |
| Style | 2 mm, much shorter than ovary | 3–4.5 mm, much longer than ovary |
The other two species found in Central Africa, N. evrardii Bamps and N. lebrunii G.C.C.Gilbert, both restricted to the Democratic Republic of the Congo, are quite different from N. camerunense, mostly due to their long and slender pedicels; N. lebrunii also has much smaller petals with a more developed inner scale, and stipules markedly bifid (to about one third of their length).
The new species also resembles Pinacopodium congolense (S.Moore) Exell & Mendonça which, as discussed in the introduction, may well be congeneric. The latter has virtually identical leaves and stipules but is usually a taller tree with a single trunk, slender pedicels, and flowers arranged in cymose inflorescences; it occurs from Gabon to Angola (Cabinda) but not in Cameroon.
The stamen filaments of N. camerunense are distinctly unequal in length (alternately long and short) but this character is not or barely noticeable in herbarium specimens, since the longer filaments tend to curve more when dried, causing all the anthers to appear at almost the same level.
CAMEROON • Ntol-Lébanga, en amont du site du projet de construction du barrage de Kikot; 4°13’55.1”N, 11°07’56.19”E; 9 Jan. 2024; Nzoyeuem et al. 261; BRLU, K, MO, P, YA • Ntol-Lébanga, en amont du site du projet de construction du barrage de Kikot; 4°15’35.53”N, 11°07’2.15”E; 11 Jan. 2024; Relevé Cameroun 126; BRLU, MO, P, YA • Nkolmelen, Île de Ponis (Nord Lebanga); 4°15’31.14”N, 11°06’48.15”E; 30 Jul. 2023; Sonké 7481; BR, BRLU, K, M, MO, P, WAG, YA • Mbébé (Silobé); 4°07’43.24”N, 11°00’12.41”E; 23 May 2024; Sonké & Ngoula 7896; BR, BRLU, K, M, MO, P, YA • Mbébé (Silobé); 4°07’44.67”N, 11°00’11.97”E; 23 May 2024; Sonké & Ngoula 7897; BR, BRLU, K, MO, P, YA • Silobé (Mbébé); 4°07’46.24”N, 11°00’12.17”E; 1 Nov. 2024; Sonké & Atangana 7929; BR, BRLU, K, M, MO, P, YA • Mbébé (Silobé); 4°07’48.1”N, 11°00’10.89”E; 28 Mar. 2025; Sonké & Ngoula 7961; BR, BRLU, K, M, MO, P, WAG, YA • Mbébé (Silobé); 4°07’44.44”N, 11°00’12.46”E; 10 May 2025; Sonké & Ngoula 7965; BR, BRLU, MO, P, YA • Mbébé (Silobé); 4°07’44.87”N, 11°00’11.84”E; 21 Nov. 2025; Sonké & Yemdji 8026; BR, BRLU, FR, K, M, MO, P, YA • Mbébé (Silobé); 4°07’41.48”N, 11°00’3.46”E; 21 Nov. 2025; Sonké & Yemdji 8027; BR, BRLU, MO, P, YA • Mbebe, en aval du site du projet de construction du barrage hydroélectrique de Kikot; 4°07’42.2”N, 11°00’4.66”E; 21 Aug. 2023; Transect Cameroun 935; BRLU, YA • Ntol (île de Ponis), en amont du site du projet de construction du barrage hydroélectrique de Kikot; 4°14’27.66”N, 11°07’23.69”E; 31 Jul. 2023; Transect Cameroun 832; BRLU, YA.
Remarkably, this locally gregarious species has apparently never been collected before 2023, with no historical specimens found in herbaria to date. This is probably due to its restricted range and habitat. Indeed, riparian forests along the Sanaga were rarely explored by botanists until recently. As discussed in the introduction, several new species were discovered during the botanical inventories carried out for the environmental impact study of the Kikot hydroelectric dam project. Furthermore, Nectaropetalum camerunense, like Talbotiella couteronii which grows in the same habitat and flowers at the same time (
The discovery of N. camerunense adds another species to the list of Sanaga Basin riverine endemics, which already includes Eugenia ancorifera Amshoff (Myrtaceae), Hibiscus elongatifolius Hochr. (Malvaceae), Maranthes sanagensis F.White (Chrysobalanaceae), Ostryocarpus zenkerianus Dunn (Fabaceae), Talbotiella couteronii (Fabaceae), Synsepalum longiflorum (Sapotaceae), Phragmanthera bidaultii (Loranthaceae), and Tristicha spinulosa (Podostemaceae). A new species of Turraea L. (Meliaceae), which is endemic to this area, is currently being described, and it is highly likely that more new species are awaiting to be discovered. Given the ongoing threats to their habitat, particularly from hydroelectric dams (three of which are already operating on the Sanaga, with another one under construction, and a further project at Kikot), there is an urgent need for further exploration and conservation measures.
We thank the herbarium staff of BR, BRLU, K, P, and YA for their assistance while working in their institutes. Thanks are due to Dr Martin Cheek (Royal Botanic Gardens, Kew) for his assistance to the first author. Special thanks are due to Dr Jeannette Mapi-Sonké for various support and advice to the first and second authors. Field work by BS, MS-D, and FN was undertaken as part of an environmental impact assessment for the Kikot hydro-electric dam project. Kikot Hydro-Power Company and Electricité de France (namely Charles Bodel, Frederick Jacob, and Antoinette Kiboum) are warmly thanked for their support to our taxonomical studies, including in the field. We thank Dr Tariq Stévart (Missouri Botanical Garden), Dr Nicolas Granier and Xavier Rufray (Biotope) for their support. Numerous site visits to monitor phenology of the novelty have been funded by IRD through the International Joint Laboratory DYCOFAC project. We would also like to thank Désiré Ntamack for his help during field work and all other collectors of specimens of the new species.