New records of Papilionoideae (Leguminosae) to Colombian flora: Lonchocarpus schiedeanus (Schltdl.) Harms and Bowdichia nitida Spruce ex Benth.
Abstract
We report the first records of Lonchocarpus schiedeanus (Schltdl.) Harms and Bowdichia nitida Spruce ex Benth. from Colombia. Lonchocarpus schiedeanus represents the first species of L. sect. Willardia in South America; this section was previously known only from Central America and the Caribbean. Bowdichia nitida is primarily known from Brazil, with scattered records in Bolivia. Our findings extend the known distributions of these species to the Colombian Orinoquia and Amazon regions. Complete descriptions, images, information about habitat, and phenology are presented.
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the journal of biodiversity data NOTES ON GEOGRAPHIC DISTRIBUTION 890 Academic editor: Marcelo Trovó Lopes deOliveira Received: 20 March 2025 Accepted: 2 July 2025 Published: 1 October 2025 Copyright © The authors. This is an open‑access article distributed under terms of the Creative Commons Attribution License (Attribution 4.0 International – CC BY 4.0) Abstract. We report the first records of Lonchocarpus schiedeanus (Schltdl.) Harms and Bowdichia nitida Spruce ex Benth. from Colombia. Lonchocarpus schiedeanus represents the first species of L. sect. Willardia in South America; this section was previously known only from Central America and the Caribbean. Bowdichia nitida is primarily known from Brazil, with scattered records in Bolivia. Our findings extend the known distri‑ butions of these species to the Colombian Orinoquia and Amazon regions. Complete descriptions, images, information about habitat, and phenology are presented. Key words. Fabaceae, Millettieae, Willardia, Bowdichia clade, South America Ariza-Cortes W, Carvajal-Rojas L, Diaz-C. SE (2025) New records of Papilionoideae (Leguminosae) to Co‑ lombian flora: Lonchocarpus schiedeanus (Schltdl.) Harms and Bowdichia nitida Spruce ex Benth. Check List 21 (5): 890–896. https://doi.org/10.15560/21.5.890 INTRODUCTION Leguminosae comprises 800 recognized genera and approximately 23,000 species (Bruneau et al. 2019). In the Neotropics, there are 314 genera (Miliken et al. 2009), and in Colombia 174 genera and 1123 species (Lewis and Castellanos 2019). The family consists of six subfamilies, five of which are represented in Colom‑ bia; Duparquetioideae is restricted to Africa (TLPWG 2017). Papilionoideae is the largest subfamily and a well‑supported monophyletic group (Kajita et al. 2001; Wojciechowski et al. 2004; TLPWG 2017). In Colombia, there are about 110 genera and 640 species of Papilionoideae (Lewis and Castellanos 2019). Lonchocarpus Kunth is a genus of more than 180 Neotropical species (Cruz‑Durán and Andrade‑Murguía 2019). Throughout its taxonomic history, various classifications have been proposed, including subgenera, series, and sections (da Silva 2010). Sousa (1992, 2009a, 2009b, 2011) and Sousa et al. (2014) outlined recent cir‑ cumscriptions. Phylogenetic studies using molecular data have validated the clustering patterns of Lonchocarpus sensu lato and reconstructed its diversification events. These studies suggest that recent evolutionary processes, occurring approximately three million years ago, primarily took place in Neotropical forests with seasonal climates (da Silva et al. 2012). The genus Bowdichia Kunth comprises two Neotropical species primarily distributed in the lowland areas of the Amazon and the Guiana Shield. It belongs to the Bowdichia clade, along with the genera Leptolobium Vogel, Guianodendron Sch. Rodr. & A.M.G. Azevedo, Diplotropis Benth., and Staminodianthus D.B.O.S. Cardoso, H.C. Lima & L.P. Queiroz (Cardoso et al. 2012; Cardoso et al. 2013). Bowdichia species are recognized by their odd‑pinnate leaves with alternate to subopposite leaflets and an emarginate apex, flowers with blue to purple petals, a suborbicular standard without auricles, wings much larger than the keels, an ovary with a capitate stigma, and samaroid, membranous, oblong fruits with the upper suture shortly winged. Bowdichia virgilioides Kunth is one of the most common trees in the wooded savannas of the Neotropical region (Conceição et al. 2011; Soares et al. 2015). Relevant studies on the biogeography of plants in the Neotropics, including the Fabaceae family, explain the migration of tree species and the origins of biodiversity in Colombia and South America (Richardson et al. 2001; Schrire et al. 2005; Pennington and Dick 2010). Several efforts have been made to document the composition and richness of the family Fabaceae in Colombia, with notable contributions from the works of Ruiz and Forero (2005) and Ariza (2022). However, gaps remain in our understanding of species distribution due to limited collections and a lack of exploration in ecologically important yet underrepresented areas of 21 (5) · https://doi.org/10.15560/21.5.890 21 (5): 890–896 New records of Papilionoideae (Leguminosae) to Colombian flora: Lonchocarpus schiedeanus (Schltdl.) Harms and Bowdichia nitida Spruce ex Benth. William Ariza-Cortes1, Lyndon Carvajal-Rojas1, Sebastian Emilio Diaz-C.2 1 Herbario Forestal (UDBC), Universidad Distrital Francisco José de Caldas, Bogotá, Colombia 2 Department of Marine, Earth, and Atmospheric Sciences, North Carolina State University, Raleigh, NC, USA Corresponding author: Sebastian Emilio Diaz-C. (sdiaz[email protected])
Check List 21 (5) · https://doi.org/10.15560/21.5.890 Ariza-Cortes et al. · New records of Lonchocarpus and Bowdichia, Colombia 891 Colombia (Castellanos and Lewis 2012). Nonetheless, recent studies have documented new records in the Colombian Orinoquia and Magdalena Valley (Mijares et al. 2017; Lucas et al. 2023). This manuscript reports the first records of species from the genera Lonchocarpus and Bowdichia within Colombia’s tropical forests. Our objectives include a comprehensive description of key morphological traits, along with photographic documentation and insights into the ecology and distribution of these species. METHODS We examined botanical collections of the genera deposited in the UDBC, LLANOS, HUA, JAUM, COAH, FMB, and COL herbaria (acronyms according to Thiers 2025) between 2022 and 2024. We also reviewed the genera using Tropicos (Missouri Botanical Garden 2025) and analyzed their type collections available on the JSTOR Global Plants platform (Ryan 2018). Additionally, we visited the Meta and Guaviare departments to monitor trees in the field. Terminology for describing leaf venations was based on Ellis et al. (2009), while the nomen‑ clature for reproductive traits followed Beentje (2016) and Alemán et al. (2020). We observed morphological traits and made measurements using a Zeiss Stemi SV 11 stereoscope. Distribution maps were created with QGIS (Rosas‑Chavoya et al. 2022) employing records from GBIF (GBIF 2023). RESULTS Lonchocarpus schiedeanus (Schltdl.) Harms Figures 1, 2 New record. COLOMBIA — Meta • Restrepo, Vereda Caney, Finca Villa Esperanza, km 5 para cruzar a Cumaral, camino a Cosmopolitana; 04°15’18.6’’N, 73°32’09.9’’W; 434 m alt.; 17.VII.2017; F. Castro leg.; 22313 Figure 1. Lonchocarpus schiedeanus. A. Trunk. B. Leaves. C. Inflorescences. D. Fruits.
Check List 21 (5) · https://doi.org/10.15560/21.5.890 Ariza-Cortes et al. · New records of Lonchocarpus and Bowdichia, Colombia 892 (UDBC) • ibid.; 30.IX.2021; W. Ariza‑C. & S.E. Díaz‑C. leg.; 9365 (COL, HUA, LLANOS, FMB, UDBC) • ibid.; 26.VII.1994; F. Castro leg.; 1131 (LLANOS) • ibid.; 30.IX.2003; F. Castro leg.; 1169 (LLANOS) • ibid.; 25.V.1994; G. Santiago leg.; 003 (LLANOS). Description. Tree up to 20 m tall, 45 cm in diameter, with a ribbed stem. Bark brown with white spots ex‑ ternally and pale yellow internally. Twigs striate, reddish brown, with lenticels. Leaves odd‑pinnate, alternate, arranged in a spiral pattern, 10.2–12.3 (–12.8) cm long; petioles 2.8–3.2 (–3.6) cm long; rachis grooved towards the apex, slightly grooved at the base; leaflets 11–13, opposite, oblong, coriaceous, sometimes with a revolute margin, with pellucid points, and papillose texture abaxially; indumentum golden, comose, and dispersed along the midvein and secondary veins abaxially, apex retuse to obtuse; venation eucamptodromous, tertiary venation black. Petiolules 1.7–2.0 mm long, grooved, drying yellowish‑brown adaxially and olive‑yellow ab‑ axially. Inflorescence in axillary pseudo‑racemes, (8.4) 11.3–16.7 (–19.7) cm long; brachyblast (2.0) 2.5–3.1 (–3.5) mm long, bearing two flowers each. Flowers papilionaceous, 16 mm long; pedicels (1.5) 2.1–2.8 (–3.0) cm long; bracteoles triangular, 0.3–0.5 mm long, positioned between the middle and apex of the pedicel; calyx pur‑ ple, (2.5) 3–3.5 (–4.0) mm long, (3.5) 3.8–4.5 (–5.0) mm wide, gamosepalous, with short lobes, less pubescent at the apex, and pellucid points; corolla pink to lilac, standard 0.7–1.1 × 0.8–1.2 cm, slightly reflexed, with a white spot at the base, suborbicular, apex emarginate, basal auricles, 0.7–1.0 mm wide, adaxially glabrescent, abaxially puberulent, claw 0.7–1.0 × 0.6 mm, wings 0.7–0.9 × 0.3–0.4 cm, falcate, auriculate base, rounded apex, abaxially puberulent, claw ca. 2 mm, keel 0.6–0.8 × 0.3–0.4 cm, oblong‑falcate, acute apex, acute base, with sparse pubescence in the lower half and pellucid points in the upper half; androecium pseudo‑mona‑ delphous, without fenestrae, isomorphic, stamens 0.9–1.1 cm long, glabrous; anthers suborbicular, basifixed, with longitudinal dehiscence; gynoecium 1.1 cm long; stigma discoidal, 0.5 mm; style linear‑curved from the base, 2 mm; ovary simple, superior, pubescent, 8–9 mm long. Fruit a samaroid legume, oblong, indehiscent, with a persistent androecium vestige at the base, (4.8) 5.2–7.8 (–10.8) cm long, (0.7) 1.0–1.4 (–1.6) cm wide, slightly thickened at the seed insertion point; seeds 1–4, reniform, concolorous. Identification. Lonchocarpus schiedeanus closely resembles Lonchocarpus castilloi Standl. but differs in its brachyblast length (2.5–3.1 mm vs. 1.6–2.1 mm in L. castilloi), calyx lobes (short vs. pronounced), fruit width (1.0–1.4 cm vs. 2–3 cm), and seed chamber (flat vs. prominent in L. castilloi). Phenology. Collected from May to July with flowers, and from August to October with fruit. Figure 2. Distribution map of Lonchocarpus schiedeanus.
Check List 21 (5) · https://doi.org/10.15560/21.5.890 Ariza-Cortes et al. · New records of Lonchocarpus and Bowdichia, Colombia 893 Bowdichia nitida Spruce ex Benth Figures 3, 4 New Records. COLOMBIA — Guaviare • San José del Guaviare, Cerro Azul, km 2, cerca de la vía; 02°33’29’’N, 72°50’51’’W; 215 m alt.; 19.X.2022; W. Ariza‑C. leg.; 9496 (UDBC) • San José del Guaviare, Carretera que conduce a Cerro Azul; 02°34’42.22”N, 73°32’9.91”W; 230 m alt.; 21.X.2023; W. Ariza‑C. & R. López leg.; 10082 (UDBC) — Guainía • Rio Inírida; 100‑600 m alt.; VII.1978; E. Acero leg.; 838 (UDBC) — vichada • Puerto Carreño, sabana entre el centro administrativo y el tapón; 10.IV.1995; M.P. Córdoba leg.; 1448 (COL). Description. Tree up to 25 m tall, with an open crown, partially deciduous; bark lenticellate with slight exfoliation in plates; exudate absent; terminal branchlets pubescent. Stipules triangular, pubescent, and caducous. Leaves imparipinnate, alternate, distichous; petiole rounded and slightly canaliculate, 1.5–3.5 cm long; rachis canaliculate, with triangular stipels 0.5–1.5 mm long; leaflets 9–15, alternate to suboppo‑ site, ovate, elliptic, oblong, or ovate‑oblong; base rounded, acute, or subcordate; apex acute to acuminate; adaxial surface glabrous; abaxial surface strigillose, golden, with scattered black trichomes; margin revolute; venation brochidodromous; secondary veins 8–15; intersecondary veins present; tertiary venation reticulate; petiolules canaliculate, 1.5–3.0 mm long, with strigose indumentum. Inflorescences in terminal panicles, up to 50 cm long; axes slightly canaliculate, strigillose; bracts triangular; bracteoles triangular to filiform, located at the base and apex of the pedicel. Flowers 1.4–1.8 cm long; pedicel 1.5–3.5 cm long; calyx turbinate, 0.6–0.8 cm long, 0.4–0.5 cm wide, purple, with triangular lobes and golden strigose indumentum; corolla lilac, petals with undulate margins; standard clawed, lamina elliptic, 1.2 × 0.8 cm; wings falcate, 13 × 6 mm; keels linear, 8 × 2 mm. Androecium with 10 free stamens; filaments 6–8 mm long; anthers rounded, basifixed, with longitudinal dehiscence. Gynoecium 1.0–1.4 cm long, with stipitate ovary; stipe 0.3 cm long; ovary 0.7–0.9 Figure 3. Bowdichia nitida. A. Trunk. B. Leaves. C. Inflorescences.
Check List 21 (5) · https://doi.org/10.15560/21.5.890 Ariza-Cortes et al. · New records of Lonchocarpus and Bowdichia, Colombia 894 cm long, with sericeous pubescence; style curved, 0.3–0.4 cm long; stigma subcapitate. Fruit a samaroid legume, oblong, elliptic to linear‑oblong, 4–8 cm × 1–2 cm, glabrous, slightly reticulate; seeds 1–6. Phenology. Collected from September to November with flowers, and from December to March with fruit. Identification. Bowdichia nitida is distinguishable from B. virgilioides by its growth form (medium‑sized to large trees vs. small trees up to 6 m), glaucous and glabrescent abaxial leaf surface (vs. generally pubescent), and more developed inflorescences. Additionally, in Colombia, B. nitida occurs mainly in forests, whereas B. virgilioides is primarily found in savannas and open areas. DISCUSSION The genus Lonchocarpus is predominantly represented in Central America. However, in recent decades, numerous taxa have been discovered in northern South America, primarily in Brazil (da Silva and Tozzi 2012). Lonchocarpus schiedeanus represents the first record of L. sect. Willardia in South America, a section previ‑ ously documented only in Central America and the Caribbean. This group is characterized by leaves with a helical arrangement, ovoid or oblong bracteoles, persistent and distant from the calyx, a glabrous corolla, and free wings of the keel (Sousa 1992). Notably, there are no records of the species on the western side of the Andes or in the inter‑Andean valleys. This new record is from the trans‑Andean zone, over the Orinoco river basin. Bowdichia is a genus represented by two species: B. nitida and B. virgilioides. The latter is generally a me‑ dium‑sized to small tree, widely distributed in South America, and abundant in wooded savannas and areas with water deficits. Conversely, B. nitida can grow up to 25 m in height. It has been primarily recorded in Brazil, with scarce records in Bolivia. It grows in forested areas of the Amazon rainforest and in regions with white sands on Precambrian shields (Cardoso et al. 2015). The two species of Bowdichia can be confused, especially in juvenile individuals. However, B. virgilioides typically exhibits abundant indumentum on the abaxial surface of its leaves and features distinctive corky bark, whereas B. nitida has leaves that are usually glaucous on the abaxial surface, with bark that is smooth or removable in plates. There is a significant gap in collections of B. nitida between the most northwestern samples in Brazil and the new records of the species in Colombia. Figure 4. Distribution map of Bowdichia nitida.
Check List 21 (5) · https://doi.org/10.15560/21.5.890 Ariza-Cortes et al. · New records of Lonchocarpus and Bowdichia, Colombia 895 In this contribution, we emphasize the importance of botanical collections and research in understand‑ ing species distributions, niches, and conservation status (Feeley and Silman 2011). Recently, new plant pop‑ ulations have been discovered at considerable distances from their known populations through herbarium reviews (da Silva et al. 2023), suggesting that sampling remains insufficient in many areas and for several taxa. Finally, we highlight the need to gather information on the population ecology of these new records. We also recommend continuing botanical explorations in these areas due to the floristic singularities that have been found; particularly in the case of L. schiedeanus, it is important to continue exploring and mon‑ itoring areas adjacent to the current record to locate additional individuals. Additionally, local propagation programs for the species are highly desirable. ACKNOWLEDGEMENTS We express our sincere gratitude to the staff at the Herbario de la Universidad de Los Llanos (LLANOS) for their collaboration in the search for botanical specimens. Additionally, we thank Diego Zapata for his sup‑ port in identifying L. schiedeanus, as well as the personnel of UDBC for their assistance. Furthermore, we are grateful to the anonymous reviewers for their valuable observations that contributed to the development of this paper. ADDITIONAL INFORMATION Conflict of interest The authors declare that no competing interests exist. Ethical statement No ethical statement is reported. Funding This study was financially supported by the authors. Author contributions Conceptualization: WAC. Data curation: WAC, LCR, SEDC. Formal analysis: WAC, LCR, SEDC. Methodology: WAC, LCR, SEDC. Resources: WAC, LCR. Visualization: WAC, LCR, SEDC. Writing – review and editing: WAC, LCR, SEDC. Author ORCID iDs William Ariza‑Cortes https://orcid.org/0000‑0002‑8423‑8256 Lyndon Carvajal‑Rojas https://orcid.org/0009‑0003‑4065‑8296 Sebastian Emilio Diaz‑C. https://orcid.org/0000‑0002‑7387‑5073 Data availability All data that support the findings of this study are available in the main text. REFERENCES Alemán MM, López-Spahr D, Gómez C, Yañez C (2020) Diversidad morfológica del androceo y gineceo de 17 especies de Papil‑ ionoideae (Fabaceae) nativas del Valle de Lerma (Salta‑Argentina) y su relación con algunos aspectos reproductivos. Boletín de la Sociedad Argentina de Botánica 55: 369–387. https://doi.org/10.31055/1851.2372.v55.n3.27867. Ariza W (2022) Sinopsis de los géneros de Leguminosae‑Papilionoideae en Colombia: árboles y arbustos. In: Forero E, Castella‑ nos C (Eds) Estudios en Leguminosas Colombianas IV. Academia Colombiana de Ciencias Exactas, Físicas y Naturales, Bogotá, Colombia, 15–136. Beentje H (2016) The Kew plant glossary: an illustrated dictionary of plant terms. Royal Botanical Garden, Kew, UK, 184 pp. Bruneau A, Borges LM, Allkin R, Egan AN, de la Estrella M, Javadi F, Klitgaard B, Miller JT, Murphy DJ, Sinou C, Vatanparast M, Zhang R (2019) Towards a new online species‑information system for legumes. Australian Systematic Botany 32: 495–518. https://doi.org/10.1071/SB19025 Cardoso D, de Lima HC, de Queiroz LP (2013) Staminodianthus, a new Neotropical genistoid legume genus segregated from Diplotropis. Phytotaxa 110: 1–16. https://doi.org/10.11646/phytotaxa.110.1.1 Cardoso D, Carvalho-Sobrinho J, Zartman C, Komura D, de Queiroz LP (2015) Unexplored Amazonian diversity: rare and phylo‑ genetically enigmatic tree species are newly collected. Neodiversity 8: 55–73. https://doi.org/10.13102/neod.81.4. Cardoso D, de Lima HC, Rodrigues RS, de Queiroz LP, Pennington RT, Lavin M (2012) The Bowdichia clade of genistoid legumes: phylogenetic analysis of combined molecular and morphological data and a recircumscription of Diplotropis. Taxon 61: 1074– 1087. https://doi.org/10.1002/tax.615012. Castellanos C, Lewis GP (2012) Leguminosas colombianas de la subfamilia Caesalpinioideae presentes en el herbario del Real Jar‑ dín Botánico de Kew, Reino Unido. Revista de la Academia Colombiana de Ciencias Exactas, Físicas y Naturales 36: 141–192. Conceição GMD, Ruggieri AC, Silva EO, Gomes EC, Roche HMV (2011) Especies vegetales y síndromes de dispersión del área de protección ambiental municipal de Inhamum, Caxias, Maranhão, Brasil. Ambiente e Agua 6: 129–142. https://doi.org/10.4136/ ambi‑agua.190.
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