identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
344687B4FFB1FE53FF38380DFA26612C.text	344687B4FFB1FE53FF38380DFA26612C.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Macropsychanthus , Harms 1900	<div><p>Macropsychanthus Harms in K. Schum. &amp; Lauterb., Fl. Schutzgeb. Südsee 366. 1900.</p><p>Type. Macropsychanthus lauterbachii Harms</p><p>Description. Lianas, less frequently shrubs. Stipules medifixed or basifixed, lanceolate or triangular. Leaves pinnately trifoliolate, stipellate or exstipellate. Inflorescence an erect and woody pseudoraceme. Flowers papilionate; calyx 4–5-lobed, rarely bilabiate; standard petal reflexed, bicallose, rarely ecallose, wing petals twice as long as or slightly longer than the keel, obliquely oblong, basal spur at the upper margin present or lacking, the keel petals naviculiform or semi-lunar, rarely straight; androecium pseudomonadelphous, anthers mostly dimorphic, 5 fertile alternating with 5 sterile, or 6 fertile and 4 sterile, less frequently all 10 fertile; ovary with 2–9 ovules, mostly sessile, rarely with a gynophore, style glabrous, cylindrical or broadened near the middle, stigma capitate. Legume turgid or slightly compressed, indehiscent or passively dehiscent, valves thick or fleshy, or fruits flat, compressed, with woody valves and elastic dehiscence, or woody and passively dehiscent or elastically dehiscent. Seeds 1–9, D-shaped to orbicular in outline, compressed or not, and lacking a particular shape, testa coriaceous; hilum short and oblong or linear and encircling 1/2 to 3/4 of the seed circumference.</p><p>Richness, distribution and habitat. Macropsychanthus comprises 52 species. The genus exhibits its greatest species richness in humid forests, with the Amazon hosting the highest number of species (20 species), followed by Southeast Asia (12) the Andes (7), and the South American Atlantic Forests (5). Although four species are found in the Caatinga and eight in the Cerrado, the genus is otherwise typically associated with wet forests.</p><p>Key to species in Southeast Asia and Oceania</p><p>1. Stipules basifixed; calyx bilabiate, with the upper lip 2-toothed and the lower lip 3-toothed...................................... M. purpureus</p><p>1. Stipules medifixed; calyx not bilabiate, with four or five lobes......................................................................................................... 2</p><p>2. Androecium with fertile anthers alternating with sterile anthers (staminodes); fruits with the pedicel attachment displaced towards the dorsal suture at the base................................................................................................................................................................ 3</p><p>2. Androecium with all ten stamens fertile; fruits with the pedicel attached near the middle of the base............................................. 5</p><p>3. Flowers 10–15 mm long; androecium with five fertile stamens and five staminodes; indumentum of young branches and inflorescence fuscous to almost black ............................................................................................................................... M. wilsonii</p><p>3. Flowers 20–25 mm long; androecium with six fertile stamens and four staminodes; indumentum of young branches and inflorescence fulvous to canescent villose or strigose.............................................................................................................................................. 4</p><p>4. Indumentum villose; bracteoles 4–5 × 5–6 mm ............................................................................................................ M. bracteosus</p><p>4. Indumentum strigose; bracteoles 1–2 × 1–2 mm ............................................................................................................ M. hexander</p><p>5. Leaflets rugose, tertiary veins strongly impressed ............................................................................................................................. 6</p><p>5. Leaflets smooth, tertiary veins not impressed .................................................................................................................................... 7</p><p>6. Flowers 25–30 mm long.............................................................................................................................................. M. ferrugineus</p><p>6. Flowers 14–17 mm long............................................................................................................................................ M. wiakabumba</p><p>7. Flowers 50–70 mm long; petals bright blue ....................................................................................................................................... 8</p><p>7. Flowers to 45 mm long; petals pink, purple or violet....................................................................................................................... 10</p><p>8. Calyx glabrous.............................................................................................................................................................. M. glabricalyx</p><p>8. Calyx hairy .........................................................................................................................................................................................9</p><p>9. Calyx with erect trichomes................................................................................................................................................ M. hirsutus</p><p>9. Calyx with adpressed trichomes................................................................................................................................. M. lauterbachii</p><p>10. Flowers 10–15 mm long; plants from the Philippines .................................................................................................... M. umbrinus</p><p>10. Flowers 40–45 mm long; plants from New Guinea, Indonesia, Caroline and Solomon Islands ..................................................... 11</p><p>11. Bracteoles 10–12 × 8–12 mm; brachyblasts 4–5.5 cm long; calyx with four lobes..................................................... M. magnificus</p><p>11. Bracteoles 4–5 × 5–6 mm; brachyblasts 5–17 mm long; calyx with five lobes......................................................... M. carolinensis</p></div>	https://treatment.plazi.org/id/344687B4FFB1FE53FF38380DFA26612C	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Fonseca-Cortés, Andrés;Clark, Ruth P.;Snak, Cristiane;Queiroz, Luciano Paganucci De	Fonseca-Cortés, Andrés, Clark, Ruth P., Snak, Cristiane, Queiroz, Luciano Paganucci De (2025): A Taxonomic Revision of Macropsychanthus (Leguminosae-Papilionoideae) Reveals New Species and New Circumscriptions in Southeast Asia and Oceania. Phytotaxa 720 (2): 93-120, DOI: 10.11646/phytotaxa.720.2.1, URL: https://doi.org/10.11646/phytotaxa.720.2.1
344687B4FFB0FE52FF383AE4FA8B6E91.text	344687B4FFB0FE52FF383AE4FA8B6E91.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Macropsychanthus bracteosus Fonseca-Cortes, R. Clark & L. P. Queiroz. A. Branch 2025	<div><p>1) Macropsychanthus bracteosus Fonseca-Cortés, R.Clark &amp; L.P. Queiroz, sp. nov.</p><p>Type: Papua, Koitaki, 6 June 1935, C.E. Carr 12552 (holotype BM-000958603!, isotypes K-000900294!, L-1953112!) . Fig. 4.</p><p>Dioclea hexandra var. carrii Amfshoff ex Hengst, in sched.</p><p>Indumento fulvo et legumine pedicello ad suturam dorsalem affixo Macropsychantho hexandro prima facie similis, sed pubescentia villosa (nec strigosa) bracteolis magnis (4–5 × 5–6 mm, nec 1–2 × 1–2 mm) distincta.</p><p>Lianas. Stems terete, brown, hollow when young; villose, fulvous or canescent on the stems, young branches, stipules, stipels, petiole, petiolules, rachis and inflorescence. Stipules 5–10 × 2–4 mm, medifixed, upper and lower lobes of similar length. Petiole 4–5 cm long, sulcate; rachis 15–20 mm long, sulcate; stipels 5–6 mm long, linear; petiolules 5–7 mm, terete; leaflets chartaceous, elliptic to ovate, base rounded, truncate, cordate or slightly attenuate, apex 4–7 mm long, mucronate or rounded; secondary veins 8–10 pairs, dorsal surface strigose fulvous, lower surface villose fulvous; lateral leaflets 5–10 × 5–7 cm; distal leaflet 5–10 × 5–7 cm. Inflorescence a pseudoraceme 18–20 cm long, erect, terminal; peduncle 2–4 cm long; brachyblasts 3–5 mm long, incurved, stalked, 5–10 mm apart; first order bract (at the brachyblast attachment) unknown; second order bract (at the pedicel attachment) 2–3 × 1–2 mm, ovate, sericeous, fulvous; bracteoles 4–5 × 5–6 mm, rounded, sericeous, fulvous; pedicel 4–6 mm long. Flowers 2–2.5 cm long; calyx 10–13 × 4–6 mm, campanulate, without a hump behind the dorsal sepal, sericeous, fulvous on the outside and velutinous fulvous on the inside; dorsal lobe 3–5 × 6–8 mm, rounded, emarginate; lateral lobes 4–6 × 3–5 mm, triangular, falcate; lower lobe 6–7 × 2–4 mm, lanceolate; petals glabrous, purple; standard petal 18–22 × 10–12 mm, elliptic, with two callosities at the base, with two basal auricles, apex emarginate, claw 3–4 × 1–2 mm; wing petals 20–25 × 10–12 mm, lower lobe rounded and rounded apex, claw 4–6 × to 1 mm, with a dorsal spur at the base of the claw; keel petals 18–20 × 10–12 mm, apex with a rounded beak, claw 4–6 × to 1 mm, with a dorsal spur at the beginning of the claw; stamens up to 20 mm long; six fertile and four infertile, ovary 4–6 mm long, 4-ovulate, covered with canescent sericeous indumentum, style to 20 mm long, linear, stigma capitate. Legume 12 cm long × 4.5 cm wide × 0.8 cm thick, oblong, laterally compressed, apex acuminate; valves woody, sericeous, fulvous, pedicel attached near the dorsal suture. Seeds not seen.</p><p>Etymology. The specific epithet is derived from the large bracteoles of this species.</p><p>Distribution and habitat. Macropsychanthus bracteosus is known only from a single locality in Papua New Guinea, where it inhabits humid forests (Fig 2A).</p><p>Preliminary conservation assessment. This species is only known from the type, collected in 1935 from eastern Papua New Guinea. Based on this single collection, the Extent of Occurrence (EOO) and Area of Occupancy (AOO) are both estimated as 4 km 2, below the thresholds for Critically Endangered under criteria B1 and B2. The type locality is in an area which is a mosaic of land cleared for agriculture and forest, although there are large areas of intact natural habitat within the elevation range of this species in eastern Papua New Guinea which have not been thoroughly explored by botanists, where it may occur. While its apparently highly restricted distribution makes this species vulnerable to stochastic effects, it is difficult to determine if it is experiencing a continuing decline given the lack of data on its current status. If found to be experiencing a continuing decline, this species could qualify as Critically Endangered under criterion B. If, however, it is not found to be threatened at its single known locality, this species would qualify for Least Concern. It is also possible that this species is much more widespread than is currently known, and it may occur at other localities in Papua and New Guinea, or even on nearby islands. As the uncertainty spans the full range of categories, we propose its classification as Data Deficient (DD) following the IUCN (2024) criteria.</p><p>Comments. Macropsychanthus bracteosus is morphologically similar to M. hexander and M. wilsonii, but can be distinguished by differences in distribution, indumentum type and color, bracteole size and keel length. Macropsychanthus bracteosus is currently known only from Papua New Guinea, although it is likely to occur on neighboring islands. Macropsychanthus hexander has a broad distribution across East Asia, Melanesia, and northern Australia. Macropsychanthus wilsonii is primarily found in the Neotropics but also occurs in French Polynesia, Madagascar and the Hawaiian Islands. Macropsychanthus bracteosus is characterized by its villose, fulvous indumentum, in contrast with the fulvous strigose or hirsute indumentum of M. hexander and the dark ferruginous, strigose or hirsute indumentum of M. wilsonii . In addition, the bracteoles of M. bracteosus measure 4–5 × 5–6 mm, which is larger than those of M. hexander and M. wilsonii (1–2 × 1–2 mm). The keel petals of M. bracteosus are 18–20 mm long, similar to those of M. hexander, but larger than the 7–10 mm long keel petals of M. wilsonii .</p></div>	https://treatment.plazi.org/id/344687B4FFB0FE52FF383AE4FA8B6E91	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Fonseca-Cortés, Andrés;Clark, Ruth P.;Snak, Cristiane;Queiroz, Luciano Paganucci De	Fonseca-Cortés, Andrés, Clark, Ruth P., Snak, Cristiane, Queiroz, Luciano Paganucci De (2025): A Taxonomic Revision of Macropsychanthus (Leguminosae-Papilionoideae) Reveals New Species and New Circumscriptions in Southeast Asia and Oceania. Phytotaxa 720 (2): 93-120, DOI: 10.11646/phytotaxa.720.2.1, URL: https://doi.org/10.11646/phytotaxa.720.2.1
344687B4FFB0FE50FF383DB0FE9A6DBA.text	344687B4FFB0FE50FF383DB0FE9A6DBA.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Macropsychanthus magnificus Fonseca-Cortes, R. Clark & L. P. Queiroz. A. Branch B. Stipule C. Inflorescence 2025	<div><p>2) Macropsychanthus magnificus Fonseca-Cortés, R.Clark &amp; L.P.Queiroz, sp. nov.</p><p>Type: Solomon Islands, Guadalcanal, <a href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=160.3&amp;materialsCitation.latitude=-9.466666" title="Search Plazi for locations around (long 160.3/lat -9.466666)">49 km from Honiara on Aola road, near Sirogharu</a>, 9 28 S 160 18 E, 16 June 1991, P.I. Forster &amp; D.J. Liddle 8598 (holotype BRI-AQ0517219!) . Fig. 5.</p><p>Ramis foliisque glabris, alabastra indumento sericeo ac flores 4–4.5 cm longis Macropsychantho carolinensi affinis, brachyblastis longioribus (4–5.5 cm, nec 0.5–1.7 cm), bracteolis maioribus (10–12 × 8–12 mm, nec 4–5 × 5–6 mm) et calyce tetralobato (nec quinquelobato) differt.</p><p>Lianas. Stems terete, brown, hollow when young; glabrous on stems, young branches, stipules, stipels, petiole, petiolules, rachis and inflorescence. Stipules 2–4 × 2–4 mm, medifixed, upper lobe larger. Petiole 8–10 cm long, sulcate; rachis 30–40 mm long, sulcate; stipels 1–2 mm long, linear; petiolules 6–8 mm, terete; leaflets chartaceous, elliptic to ovate, base rounded, truncate or cordate, apex 4–7 mm long, mucronate or rounded; secondary veins 7–11 pairs, dorsal surface and lower surface glabrous; lateral leaflets 8–20 × 8–13 cm; distal leaflet 8–23 × 8–13 cm. Inflorescence a pseudoraceme 65 cm long, erect, axillary; peduncle 30 cm long; brachyblasts 4–5.5 cm long, straight, 10–25 mm apart; first order bract (at the brachyblast attachment) unknown; second order bract (at the pedicel attachment) 2–3 × 1–2 mm, ovate, sericeous, canescent; bracteoles 10–12 × 8–12 mm, rounded, sericeous, canescent; pedicel 8–10 mm long. Flowers 4–4.5 cm long; calyx 18–22 × 8–12 mm, 4-lobed, tubular, without a hump behind the dorsal sepal, canescent sericeous; dorsal lobe 8–10 × 8–10 mm, triangular; lateral lobes 8–10 × 4–7 mm, triangular; lower lobe 8–10 × 4–7 mm, triangular; petals glabrous, pink; standard petal 30–35 × 18–22 mm, elliptical, with two callosities at the base, without basal auricles, apex emarginate, claw 3–4 × 1–2 mm; wing petals 28–35 × 12–16 mm, lower lobe rounded, apex rounded, claw 5–7 × up to 1 mm, with a dorsal spur at the beginning of the claw; keel petals 30–37 × 10–12 mm, apex with a rounded beak, claw 4–6 × to 1 mm, with a dorsal spur at the beginning of the claw; stamens up to 35 mm long, all fertile; ovary 4–6 mm long, 4-ovulate, covered with canescent sericeous indumentum, style to 30 mm long, linear, stigma capitate. Legume and seeds unknown.</p><p>Etymology. The specific epithet comes from the Latin word magnificus, meaning “splendid”, referring to the striking inflorescences of this species.</p><p>Distribution and habitat. Macropsychanthus magnificus is known only from Guandacanal (Solomon Islands), where it inhabits humid and riverine forests (Fig 3E).</p><p>Preliminary conservation assessment. This species is only known from two collections comprising two separate locations on Guadalcanal in the Solomon Islands. The Extent of Occurrence is estimated as 8-44 km 2 and the Area of Occupancy (AOO) as 8 km 2, both falling below thresholds for a threatened category under criteria B1 and B2 respectively. However, this area has not been intensively explored by botanists and it is possible that this species occurs on other islands, in which case the EOO and AOO could be much larger. Much of the lowland forest on Guadalcanal has been cleared for agriculture, settlements, and plantations (Olson 2025). These threats are inferred to be contributing to a continuing decline in the area, extent, and quality of habitat for this species. Given the available data, we take a precautionary approach here and propose this species is classified as Endangered B1ab(iii)+2ab(iii) following the IUCN (2024) criteria.</p><p>Comments. This species is unusual within the genus due to its larger brachyblasts, measuring 4–5.5 cm in length, and its bracteoles, which measure 10–12 × 8–12 mm. Morphologically, it resembles M. carolinensis in the presence of sericeous indumentum on the inflorescence and flower buds, and flowers, which are 4–4.5 cm long. However, M. carolinensis differs by having significantly smaller brachyblasts (5–17 mm long) and bracteoles (4–5 × 5–6 mm).</p><p>Paratype. Solomon Islands, Guadalcanal, Umasami river, 5 miles inland, 3 July 1965, Whitmore 6010 (K-000980361) .</p></div>	https://treatment.plazi.org/id/344687B4FFB0FE50FF383DB0FE9A6DBA	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Fonseca-Cortés, Andrés;Clark, Ruth P.;Snak, Cristiane;Queiroz, Luciano Paganucci De	Fonseca-Cortés, Andrés, Clark, Ruth P., Snak, Cristiane, Queiroz, Luciano Paganucci De (2025): A Taxonomic Revision of Macropsychanthus (Leguminosae-Papilionoideae) Reveals New Species and New Circumscriptions in Southeast Asia and Oceania. Phytotaxa 720 (2): 93-120, DOI: 10.11646/phytotaxa.720.2.1, URL: https://doi.org/10.11646/phytotaxa.720.2.1
344687B4FFB2FE5DFF383EA7FF676100.text	344687B4FFB2FE5DFF383EA7FF676100.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Macropsychanthus wiakabumba Fonseca-Cortes, R. Clark & L. P. Queiroz. A. Branch 2025	<div><p>3) Macropsychanthus wiakabumba Fonseca-Cortés, R.Clark &amp; L.P.Queiroz, sp. nov.</p><p>Type: Papua New Guinea, District Morobe, Subdistrict Lae, <a href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=146.83333&amp;materialsCitation.latitude=-6.8333335" title="Search Plazi for locations around (long 146.83333/lat -6.8333335)">about 2 km south of Timini village, along Lae-Bulolo road</a>, 6°50’S 146°50’E, 9 May 1977, J. Wiakabu &amp; T. Umba 70394 (holotype: NSW-863173!; isotypes: A-2261614!, BISH, BM, BO, BRI-AQ355171!, CANB-00549252!, E!, K-0009800354!, L-1953109!, M, PNH, QRS, SING, US-02343836!) . Fig. 6.</p><p>Combinatione foliolis rugosis 8–11 paribus venarum donatis, floribus 1.4–1.7 cm longis vexillo 10–14 × 6–8 mm, alis 12–14 × 4–6 mm et carina 12–15 × 3–6 mm, atque decem staminibus fertilibus, inter species generis unica.</p><p>Lianas. Stems terete, brown, hollow when young; hirsute and fulvous on the stems, young branches, stipules, stipels, petiole, petiolules, rachis and inflorescence. Stipules 10–20 × 2–4 mm, medifixed, upper and lower lobes of similar length. Petiole 7–13 cm long, sulcate; rachis 20–30 mm long, sulcate; stipels 5–7 mm long, linear; petiolules 7–10 mm, terete; leaflets chartaceous, elliptic to ovate, base rounded, truncate, cordate or slightly attenuate, apex 5–10 mm long, mucronate or rounded; secondary veins 9–11 pairs, dorsal and lower surface strigose fulvous; lateral leaflets 10–14 × 8–10 cm; distal leaflet 12–15 × 8–10 cm. Pseudoraceme 55–85 cm, erect, axillary or terminal; peduncle of inflorescence 30–45 cm long; brachyblasts 3–7 mm, incurved, stalked, 5–15 mm apart; first-order bract (at the brachyblast attachment) 7–12 × 2–3 mm, lanceolate, erect or reflexed; second-order bract (at the pedicel attachment) 1–2 × 1–2 mm, ovate, sericeous, fulvous; bracteoles 1–2 × 1–2 mm, rounded, sericeous, fulvous; pedicel 4–6 mm long. Flowers 1.4–1.7 cm long; calyx 5–7 × 5–7 mm, campanulate, without a hump behind the dorsal sepal, strigose, fulvous on the outside and velutinous fulvous on the inside; dorsal lobe 3–4 × 4–6 mm, rounded, emarginate; lateral lobes 3–5 × 3–5 mm, triangular, falcate; lower lobe 3–4 × 2–4 mm, lanceolate; petals glabrous, purple; standard petal 10–14 × 6–8 mm, elliptic, with two callosities at the base, with two basal auricles, apex emarginate, claw 3–4 × 1–2 mm; wing petals 12–14 × 4–6 mm, lower lobe rounded, apex rounded, claw 4–5 × to 1 mm, with a dorsal spur at the base of the claw; keel petals 12–15 × 3–6 mm, apex with one rounded beak, claw 4–6 × to 1 mm, with a dorsal spur at the beginning of the claw; stamens up to 15 mm long; all fertile, ovary 5–8 mm long, 3-ovulate, covered with canescent sericeous indumentum, style up to 5 mm long, linear, stigma capitate. Legume and s eeds unknown.</p><p>Etymology. The specific epithet honors J. Wiakabu and T. Umba for their contributions to advancing knowledge of the flora of Papua New Guinea.</p><p>Distribution and habitat. Macropsychanthus wiakabumba is known only from a single locality in Papua New Guinea (Fig. 3F).</p><p>Preliminary conservation assessment. This species is only known from the type, collected in 1935 from eastern Papua New Guinea. Based on this single collection, the Extent of Occurrence (EOO) and Area of Occupancy (AOO) are both estimated as 4 km 2, below the thresholds for Critically Endangered under criteria B1 and B2. The single known collection was made in disturbed lowland forest, and much of the area surrounding the type locality within the elevation range of this species is a mosaic of land cleared for shifting agriculture and secondary forest. However, this species may be able to persist in secondary forest as observed for other species in the genus. While its apparently highly restricted distribution makes this species vulnerable to stochastic effects, it is difficult to determine if it is experiencing a continuing decline given the lack of data on its population status. If found to be experiencing a continuing decline, this species could qualify as Critically Endangered under criterion B. If, however, it is not found to be threatened at its single known locality, this species would qualify for Least Concern. It is also possible that this species is much more widespread than is currently known, and it may occur at other localities in Papua and New Guinea, or even on nearby islands. As the uncertainty spans the full range of categories, we propose its classification as Data Deficient (DD) following the IUCN (2024) criteria.</p><p>Comments. Macropsychanthus wiakabumba exhibits a distinctive morphology not observed in any other species of Macropsychanthus, particularly in its rugose leaflets with 8–11 pairs of secondary veins, very small flowers (1.4–1.7 cm long), standard petal 10–14 × 6–8 mm, wing petals 12–14 × 4–6 mm, keel petals 12–15 × 3–6 mm and ten fertile stamens. In vegetative morphology, it resembles M. ferrugineus and M. hexander due to the presence of a hirsute indumentum and a similar number of secondary veins in the leaflets. However, M. hexander is distinguished by its larger flowers (2–2.5 cm long), standard petal 17–20 × 13–17 mm, wing petals 17–20 × 7–12 mm, keel petals 14–18 × 7–12 mm, and six fertile stamens and four staminodes. In contrast, M. ferrugineus has flowers measuring 2.5–3 cm long, standard petal 25–30 × 18–22 mm wing petals 25–30 × 10–12 mm, keel petals 25–30 × 10–12 mm, and ten fertile stamens.</p></div>	https://treatment.plazi.org/id/344687B4FFB2FE5DFF383EA7FF676100	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Fonseca-Cortés, Andrés;Clark, Ruth P.;Snak, Cristiane;Queiroz, Luciano Paganucci De	Fonseca-Cortés, Andrés, Clark, Ruth P., Snak, Cristiane, Queiroz, Luciano Paganucci De (2025): A Taxonomic Revision of Macropsychanthus (Leguminosae-Papilionoideae) Reveals New Species and New Circumscriptions in Southeast Asia and Oceania. Phytotaxa 720 (2): 93-120, DOI: 10.11646/phytotaxa.720.2.1, URL: https://doi.org/10.11646/phytotaxa.720.2.1
344687B4FFBEFE5AFF383CF1FEEF6A84.text	344687B4FFBEFE5AFF383CF1FEEF6A84.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Macropsychanthus carolinensis Kanehira & Hosokawa, Trans. Nat. Hist. Soc.	<div><p>4) Macropsychanthus carolinensis Kanehira &amp; Hosokawa, Trans. Nat. Hist. Soc. Taiwan 24: 414. 1934.</p><p>Type. Caroline Islands, Palau, August 1931, Kanehira 1711 (holotype: TAI-118892!; isotypes: NY- 04814511!, P-02752991!) . Fig. 7.</p><p>Macropsychanthus dolichobotrys Holth., Blumea 5: 192. 1942. Type. Indonesia, Talaud Islands, Pasir Malap, 14 May 1926, Lam 3002 (holotype: L-0019084!; isotypes: BO, L-0019085!, L- 0019086!), syn. nov.</p><p>Macropsychanthus lauterbachii subsp. parviflorus Verdc., Kew Bull. 32(2): 456-457.1978. Macropsychanthus lauterbachii var. parviflorus (Verdc.) Adema, Blumea 43: 236. 1998. Type. Papua New Guinea, Milne Bay District, Rossel Island, 5 October 1956, Brass 28335 (holotype: K! K-000900300; isotypes: A-00057466!, L-0019089!, L-0019090!, LAE, S-10- 10521!, US-00170445!), syn. nov.</p><p>Macropsychanthus lauterbachii subsp. neobritannicus Verdc., Kew Bull. 32(2): 456-457. 1978. Type: Papua New Guinea, New Britain, Talasea subdistrict, Kopiura river, 15 May 1968, Henty in NGF 29391 (holotype: LAE; isotypes: A-00057465!, BOG, BRI-AQ0052463!, CANB, K-000900299!, L-0019091!, SING), syn. nov.</p><p>Diagnostic description. Lianas glabrescent, with sericeous canescent indumentum restricted to the inflorescence. Leaflets with smooth surfaces and 7–10 pairs of secondary veins. Flowers 4–4.5 cm long, calyx with five lobes, ten fertile stamens. Legume 10–17 cm long × 4–6 cm wide × 1.5–2 cm thick, glabrous, laterally compressed, pedicel attachment displaced toward the dorsal suture. Seeds 2.5–3 cm long × 2.5–3 cm wide × 1.0– 1.5 cm thick, D-shaped or orbicular in outline, black, smooth.</p><p>Etymology. The specific epithet refers to the Caroline Islands, where the holotype of the species was collected.</p><p>Distribution and habitat. This species occurs in Papua New Guinea, the Caroline and Solomon islands, and Indonesia, at elevations between 0–50 m a.s.l., where it inhabits humid and riverine forests (Fig. 3A).</p><p>Preliminary conservation assessment. This species is widely distributed across several islands, and has a large Extent of Occurrence (EOO) of 3,924,472 km ², far exceeding the threshold for a threatened category under criterion B1. Based on herbarium specimen records, the Area of Occupancy (AOO) is estimated as 36 km ². The AOO is likely an underestimate given that botanical collection efforts have been limited in some parts of this species’ range, however it is considered unlikely that the true value exceeds the threshold for a threatened category under criterion B2. This species is known from nine localities across nine different islands. However, most of the islands that this species has been collected from have large areas of intact forest with no obvious threats. As such, the locations concept cannot be used and the species is not thought to be undergoing a continuing decline. Considering these factors, propose classifying this species as Least Concern (LC), following the IUCN (2024) criteria.</p><p>Comments. Macropsychanthus carolinensis closely resembles M. magnificus in overall morphology, particularly in the presence of a sericeous indumentum on the inflorescence, similar flower bud shape, and comparable flower length. However, M. carolinensis can be distinguished by its smaller brachyblasts (5–17 mm long) and bracteoles (4–5 × 5–6 mm).</p><p>Specimens examined. FEDERATED STATES OF MICRONESIA, Caroline Islands, Truk Moen, Aug 1931, Kanchira 1711 (NY, P, TAI). INDONESIA, Talaud island, Talaud, Karakelang; pasir Malap, E. of Lobo, 14 May 1926, Lam 3002 (L); Talaud island, Talaud Karakelang; S.W. slope of G. Duata, 8 May 1926, Lam 2893 (L). PAPUA NEW GUINEA, Mumma River, 20 May 1926, Brass 1519 (AAH, CANB, K); Milne Bay, Sudest Is., 28 Jan 2009, Johns 12764 (K); Milne Bay, Rossel Isl., Abaleti, 5 Oct 1956, Brass 28335 (AAH, K, L, US); Morobe, Kapiura river, at Junction with Karoli river, near Lavege village, N.B., 5.65º S, 150.62º E, 15 March 1968, Henty 29391 (AAH, BRI, BO, K, L). SOLOMON ISLANDS, Guadalcanal, 5 miles inland, N.W Guadalcanal, 14 July 1965, Whitmore 6088 (BRI, CANB, K, L, P); Makira-Ulawa, San Cristobal, ridge east of Pegato. Ridge forest, 3 August 1965, Fergusson 2315 (BRI, CANB, K, L, P); New Georgia, Baga Island, Valley bottom, 14 June 1965, Whitmore 2913 (L, K); New Georgia, Tita River, S.E Georgia, 14 Jun 1965, Maenu’u 5990 (L); New Georgia, Tita River, 27 April 1966, Burn-Murdoch 7187 (K).</p></div>	https://treatment.plazi.org/id/344687B4FFBEFE5AFF383CF1FEEF6A84	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Fonseca-Cortés, Andrés;Clark, Ruth P.;Snak, Cristiane;Queiroz, Luciano Paganucci De	Fonseca-Cortés, Andrés, Clark, Ruth P., Snak, Cristiane, Queiroz, Luciano Paganucci De (2025): A Taxonomic Revision of Macropsychanthus (Leguminosae-Papilionoideae) Reveals New Species and New Circumscriptions in Southeast Asia and Oceania. Phytotaxa 720 (2): 93-120, DOI: 10.11646/phytotaxa.720.2.1, URL: https://doi.org/10.11646/phytotaxa.720.2.1
344687B4FFB8FE5AFF3839CCFD1C6120.text	344687B4FFB8FE5AFF3839CCFD1C6120.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Macropsychanthus ferrugineus Merr., Philipp. J. Sc.	<div><p>5) Macropsychanthus ferrugineus Merr., Philipp. J. Sc. 5, Bot.: 121. 1910.</p><p>Type. Philippines, Mindanao, Lake Lanao, w.d., Clemens 419 (lectotype, designated by Adema 1998: US-00004643!; isolectotypes: F-0059545!, K-000900292!, K-000900293!) . Fig. 8.</p><p>Dioclea decandra Amshoff ex Adema, Blumea 43: 234. 1998.</p><p>Diagnostic description. Lianas with fulvous indumentum. Leaflets with rugose upper surface and 11–12 pairs of secondary veins. Flowers 2.5–3.0 cm long, calyx with four lobes, ten fertile stamens. Legume 10–12 cm long × 4–4.5 cm wide × 1.5–2 cm thick, fulvous strigose, laterally compressed, pedicel attachment displaced toward the dorsal suture. Seeds 2–2.5 cm long × 1–1.5 cm wide × 1–1.5 cm thick, orbicular in outline, black, smooth.</p><p>Etymology. The specific epithet comes from the Latin word ferrūgineus, meaning “rusty”, alluding to the goldencolored indumentum of the fruit.</p><p>Distribution and habitat. Macropsychanthus ferrugineus is endemic to the Philippines, where it occurs in riverine forests (Fig. 2B).</p><p>Preliminary conservation assessment. The Extent of Occurrence (EOO) is estimated as 203,329 km 2, which greatly exceeds thresholds for a threatened category under criterion B1. Based on herbarium specimen records, the Area of Occupancy (AOO) is estimated as 40 km ². The AOO is likely an underestimate given that botanical collection efforts have been limited in some parts of this species’ range, however it is considered unlikely that the true value exceeds the threshold for a threatened category under criterion B2. It is only known from ten locations, with no new collections since 1995. It is inferred to be undergoing a continuing decline in the area and quality of its habitat due to deforestation associated with settlement expansion. Considering these factors, we propose classifying this species as Vulnerable B2ab(iii), following the IUCN (2024) criteria.</p><p>Comments. Macropsychanthus ferrugineus is characterized by its rugose leaflets with 11–12 pairs of secondary veins, pink flowers, a 4-lobed sericeous calyx, flowers measuring 2.5–3.0 cm in length, and ten fertile stamens. This species is readily distinguishable from other Southeast Asian species, although it bears some resemblance to M. hirsutus due to its rugose leaflets. However, M. hirsutus differs by having leaflets with 8–10 pairs of secondary veins, blue flowers, a 4-5-lobed hirsute calyx, and significantly larger flowers (5–7 cm long).</p><p>Specimens examined. PHILIPPINES. Agusan, Cabadbaran (Mt. Urdaneta), island of Mindanao, October 1912, Elmer 13993 (NSW, US); Island of Mindanao, October 1912, Elmer 13993 (US); Bohol, Aug–Oct 1923, Ramos 43301 (US); Cebu, November 1995, Bicknell 931 (L); Mindanao, Lake Lanao, September–October 1906, Clemens 419 (US, K, F); Palawan, Busuanga island, Sep 1922, Ramos 41220 (US); Panay, Capiz, October–November 1925, Edaño 46013 (US); Zamboanga, Malangas, October–November 1919, Ramos 36747 (US); Zamboanga, Malangas, October–November 1919, Ramos 36821 (US).</p></div>	https://treatment.plazi.org/id/344687B4FFB8FE5AFF3839CCFD1C6120	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Fonseca-Cortés, Andrés;Clark, Ruth P.;Snak, Cristiane;Queiroz, Luciano Paganucci De	Fonseca-Cortés, Andrés, Clark, Ruth P., Snak, Cristiane, Queiroz, Luciano Paganucci De (2025): A Taxonomic Revision of Macropsychanthus (Leguminosae-Papilionoideae) Reveals New Species and New Circumscriptions in Southeast Asia and Oceania. Phytotaxa 720 (2): 93-120, DOI: 10.11646/phytotaxa.720.2.1, URL: https://doi.org/10.11646/phytotaxa.720.2.1
344687B4FFBBFE47FF383CE5FE106860.text	344687B4FFBBFE47FF383CE5FE106860.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Macropsychanthus glabricalyx (Verdc.) Fonseca-Cortes, R. Clark & L. P. Queiroz 2025	<div><p>6) Macropsychanthus glabricalyx (Verdc.) Fonseca-Cortés, R.Clark &amp; L.P.Queiroz, comb. nov.</p><p>Macropsychanthus lauterbachii subsp. glabricalyx Verdc., Kew Bull. 32(2): 456. 1978.</p><p>Type. Papua New Guinea, Northern District, near Kokoda, 21 September 1953, Hoogland 3953 (holotype: K-000900297!; isotypes: A-00057463!, BM-000958600! BM-000958601!, BRI- AQ0050313!, CANB-74008.1!, L-0019087!, LAE, MEL-81601!, US-00170444!) . Fig. 9.</p><p>Diagnostic description. Lianas glabrescent. Leaflets with smooth surfaces and 6–8 pairs of secondary veins. Flowers 5–7 cm long, calyx with four lobes and ten fertile stamens. Legume and seeds unknown.</p><p>Etymology. The specific epithet is derived from the Latin words glaber (meaning “glabrous”) and calyx, referring to the glabrous calyx that characterizes this species.</p><p>Distribution and habitat. Macropsychanthus glabricalyx is known only from Papua New Guinea, where it inhabits riverine forests in altitudes close to sea level (Fig. 3B).</p><p>Preliminary conservation assessment. This species is only known from three collections, the most recent of which dates from 1953. Two collections are from near Kokoda, where much of the natural habitat within the elevation range of this species has been cleared for agriculture. A third specimen was collected in 1920 somewhere along the Mamberamo River in Papua, however the exact locality is not known. If restricted to a single location in the highly transformed river valley near Kokoda, this species could be threatened with an EOO and AOO as small as 4-8 km 2, qualifying for Critically Endangered. However, given the disjunct occurrence in Papua this species could have a much larger range, and may occur in areas of intact lowland forest where botanical collecting efforts have been low, such that it would qualify for Least Concern. Given that the uncertainty spans the full range of categories, we propose classifying this species as Data Deficient (DD), in accordance with IUCN (2024) criteria.</p><p>Comments. Macropsychanthus glabricalyx is similar to M. lauterbachii in its overall glabrescent aspect. However, it can be easily distinguished by its leaflets, which have 6–8 pairs of secondary veins, and a glabrous calyx. In contrast, M. lauterbachii has leaflets with 8–11 pairs of secondary veins and a calyx covered in sericeous indumentum, which may be fulvous or canescent.</p><p>Specimens examined. PAPUA NEW GUINEA, Kokoda, 9 Oct 1933, Chesman 108 (K); bank Othe river, 29 June 1920, Lam 466 (L).</p></div>	https://treatment.plazi.org/id/344687B4FFBBFE47FF383CE5FE106860	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Fonseca-Cortés, Andrés;Clark, Ruth P.;Snak, Cristiane;Queiroz, Luciano Paganucci De	Fonseca-Cortés, Andrés, Clark, Ruth P., Snak, Cristiane, Queiroz, Luciano Paganucci De (2025): A Taxonomic Revision of Macropsychanthus (Leguminosae-Papilionoideae) Reveals New Species and New Circumscriptions in Southeast Asia and Oceania. Phytotaxa 720 (2): 93-120, DOI: 10.11646/phytotaxa.720.2.1, URL: https://doi.org/10.11646/phytotaxa.720.2.1
344687B4FFA5FE45FF383BE0FEF568DF.text	344687B4FFA5FE45FF383BE0FEF568DF.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Macropsychanthus hexander (Ralph) L. P. Queiroz & Snak, PhytoKeys 2020	<div><p>7) Macropsychanthus hexander (Ralph) L.P. Queiroz &amp; Snak, PhytoKeys 164: 97, 2020.</p><p>Mucuna hexandra Ralph, IC. Carp., 30, t. 34, f. 5. 1849. Dioclea hexandra (Ralph) Mabb., Taxon 29(5–6): 605–606, 1980.</p><p>Type: The plate of Dolichos hexandrus Roxb. (nom. nud.), Ic. 2328 (holotype K) . Fig 10.</p><p>Dolichos coriaceus Graham ex Wall., Numer. List [Wallich] n. 5562. 1831, nom. inval. (nom. nud.). Dioclea coriacea (Graham ex Wall.) Rusby, Mem. Torrey Bot. Club 3(3): 22. 1893. Type: Singapore, Penang, w.d., Wallich 5562 (holotype: K-001121297!).</p><p>Dioclea javanica Benth., Pl. Jungh. 2: 236. 1852. Macropsychanthus javanicus (Benth.) L.P. Queiroz &amp; Snak, PhytoKeys 164, 2020. Type: Indonesia, Java, w.d., Junghuhn s.n. [=108?] (lectotype, designated by Queiroz &amp; Snak (2020): K-000898373!; isolectotype: L-0018938!). syn. nov.</p><p>Dioclea fergusonii Thwaites, Enum. Pl. Zeyl. 5: 412. 1864. Type: Sri Lanka, near Colombo, 1866, Ferguson 3817 (lectotype here desginated: BM-000958602!; isolectotypes: G-00364007!, K-000898372!, P-00708478!).</p><p>Macropsychanthus novoguineensis Pulle, Nova Guinea 8: 382. 1910. Type: Indonesia, Irian Jaya, May 1907, Versteeg 1028 (lectotype designated by Queiroz &amp; Snak (2020): L-0018939!; isolectotypes: BO, U-1248394!).</p><p>Dioclea hexandra var. merrillii Amshoff ex den Hengst, in sched.</p><p>Dioclea hexandra var. australiensis Domin, in sched.</p><p>Dioclea hexandra var. javanica (Benth.) den Hengst, in sched.</p><p>Dioclea reflexa var. javanica (Benth.) den Hengst, in sched.</p><p>Diagnostic description. Lianas with fulvous indumentum. Leaflets with smooth surfaces and 8–11 pairs of secondary veins. Flowers 2–2.5 cm long, calyx with four lobes, six fertile stamens and four staminodes. Legume 7–12 cm long × 4–5.5 cm wide × 0.8–1.5 cm thick, fulvous strigose, laterally compressed, pedicel attachment displaced toward the dorsal suture. Seeds 3–3.5 cm long × 3–3.5 cm wide × 1–1.5 cm thick, D-shaped, black, smooth.</p><p>Etymology. The specific epithet alludes to the six fertile stamens in this species.</p><p>Distribution and habitat. This species has a broad distribution across Southeast Asia, present in Australia, Brunei, India, Indonesia, Malaysia, Myanmar, Papua New Guinea, Philippines, Solomon Islands, Sri Lanka, and Thailand. It occurs in humid, riverine, and disturbed forests, as well as near beaches (Fig. 2C).</p><p>Preliminary conservation assessment. The Extent of Occurrence (EOO) is estimated at 15,361,495 km 2, which greatly exceeds thresholds for a threatened category under criterion B1. The Area of Occupancy (AOO) is estimated as 208 km 2, which would meet the threshold for Endangered (EN) under criterion B2. However, the AOO should be considered a minimum estimate since botanical collection efforts have been limited in some parts of this species’ range. The species is neither severely fragmented nor undergoing a continuous decline. Furthermore, it is known from many more than ten locations. Considering these factors, we propose classifying this species as Least Concern (LC) following IUCN (2024) criteria.</p><p>Comments. Macropsychanthus hexander may be confused with M. wilsonii due to the similar number of secondary veins and the fruit morphology, particularly the pedicel attachment displaced toward the dorsal suture. However, M. hexander is distinguished by its fulvous indumentum, flowers measuring 2–2.5 cm long, six fertile stamens and four staminodes, and seeds measuring 3–3.5 cm long × 3–3.5 cm wide × 1–1.5 cm thick. In contrast, M. wilsonii has a dark ferruginous indumentum, smaller flowers (1–1.5 cm long), five fertile stamens and five staminodes, and seeds measuring 25–30 mm long, 15–25 mm wide, 10–15 mm thick.</p><p>Some of the exsiccatae housed in L bear the names Dioclea hexandra var. merrillii Amshoff ex den Hengst, Dioclea hexandra var. javanica (Benth.) den Hengst, Dioclea reflexa var. javanica (Benth.) den Hengst, and Dioclea hexandra var. australiensis Domin. However, none of these names were ever validly published.</p><p>Specimens examined. AUSTRALIA, Queensland, Cook District, 7 Dec 1941, White 11691 (BRI). BRUNEI, Tutong, Rambai, Kampong Panchong, 4º 58′ N, 114º 72′ E, 22 June 1995, Namgkat et al. 16801 (K, L). MYANMAR, Tenasserim, Tavoy district, 14º N, 98º 5′ E, October 1961, Keenan et al. 1945 (RBGE). INDIA, Andamans, Ali Wastid Reserve, 27 January 1918, Parkinson 245 (K). INDONESIA, Amboina, July–November 1913, Robinson 2048 (US); Borneo, Soengai Tanggi, 1893–1894, Hallier 1002 (L); Buru, Wacha R. N. Buru, between Wawlanga and laje Kunturun, riverine forest dominated by Neonauclea, 14 November 1984, Balgooy 4766 (K, L); Celebes, Sulawesi Selatan, N. shore of lake Mata-no, Donemaitu, 2° 33′ S, 121° 45′ E, 11 August 1979, Vogel 6210 (L); Kalimantan Timur, between Long Bawan and Panado, 3º 87′ N, 115° 7′ E, 10 July 1981, Geesink 9003 (L); Lesser Sunda Islands, 1973, Schmutz 5852 (L); Moluccas, Seram, Manusela National Park: a low hill north of Kanikeh, Kecamatan (District) Seram Utara, 3º 1′ S, 129º 22′ E, 4 January 1985, Kato et al. 3080 (L); Sumatra, Tapianoeli, division Padang Si Dimpoean, subdivision Padang Lawas, 21–27 September 1933, Liman 5622 (L, US); Sungai, Kelindjau R. (W. Kutei), flatland, Segoi, 12 June 1954, Kostermens 9584 (K, L); MALAYSIA, Sabah, Keningau, 22 Jun 1989, Asik 127658 (L); Sarawak, Baram district, October 1894, Home 326 (L); Selangor, Batu Tiga, May 1902, Curtis 3766 (K); Tregganum, Passir Gajah: Ulu Kemaman.Roadside verge, 10 August 1977, Lewis 129 (L). PAPUA NEW GUINEA, Lower Fly River, east bank opposite Sturt Island, October 1936, Brass 8231 (BRI, K, L); Fergusson, 23 June 1956, Brass 27299 (L); East Setik, Ambunti district. Waskuk hill, buttress ridge N of Garuka Foothill forest, 4° 18′ S, 142° 73′ E, 24 Nov 2001, Takeuchi et al. 17449 (L); Madang, Road No. 1 near Mawan village, Gogol valley. Subdist. Madang, 5° 22′ S, 145 58º E, 26 January 1977, Wiakabu et al. 70365 (BRI, L, K); Malalaua, Near Malalaua, Gulf District, Papua, 2 March 1966, Craven &amp; Schodde 931 (L, K); Morobe, Bambu River, near Lae, Lae sub-dist., 6 °75′ S, 147º E, 1 September 1970, Womersley 43664 (BRI, L, K); Tagula, Sudest isl.; Rambuso, 15 September 1956, Brass 28100 (L). PHILIPPINES, Luzon, Rizal province, September 1905, Ahern 333 (K, US); Mindoro, Baco river, March 1905, Elmer 4033 (US, K, L); Palawan, Forest N of Tagburos c. km 17 N of P. Princess, 27 October 1985, Ridsdale 1091 (L). SOLOMON ISLANDS, Bongainville, December 1931, Waterhouse 662 (K). SRI LANKA, Ceylán, Macrae, w.d., w.c (L-1952864). THAILAND, Narathiwat, Sue-ngai Kolok Toe Daeng Peat Swamp Forest, 9 May 2005, Niyondham &amp; Puudjaa 7381 (K).</p></div>	https://treatment.plazi.org/id/344687B4FFA5FE45FF383BE0FEF568DF	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Fonseca-Cortés, Andrés;Clark, Ruth P.;Snak, Cristiane;Queiroz, Luciano Paganucci De	Fonseca-Cortés, Andrés, Clark, Ruth P., Snak, Cristiane, Queiroz, Luciano Paganucci De (2025): A Taxonomic Revision of Macropsychanthus (Leguminosae-Papilionoideae) Reveals New Species and New Circumscriptions in Southeast Asia and Oceania. Phytotaxa 720 (2): 93-120, DOI: 10.11646/phytotaxa.720.2.1, URL: https://doi.org/10.11646/phytotaxa.720.2.1
344687B4FFA7FE44FF383B83FD2F6DA4.text	344687B4FFA7FE44FF383B83FD2F6DA4.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Macropsychanthus hirsutus (Fonseca-Cortes, R. Clark & L. P. Queiroz. A. Branch B. Stipule C. Inflorescence D. Flower 2025) Fonseca-Cortes, R. Clark & L. P. Queiroz. A. Branch B. Stipule C. Inflorescence D. Flower 2025	<div><p>8) Macropsychanthus hirsutus (Verdc.) Fonseca-Cortés, R.Clark &amp; L.P.Queiroz, comb. nov.</p><p>Macropsychanthus lauterbachii var. hirsutus Verdc., Kew Bull. 32(2): 456. 1978.</p><p>Type. Papua New Guinea, Morobe District: near Lae, 21 August 1961, Millar in NGF 13819 (holotype: K-000900298!; isotypes: A-00057464!, E-00531192!, BRI-AQ0050930!, L-0019088!, LAE) . Fig. 11.</p><p>Diagnostic description. Lianas with hirsute fulvous indumentum. Leaflets with either smooth or rugose upper surface and 8–10 pairs of secondary veins. Flowers 5–7 cm long, calyx with four or five lobes, ten fertile stamens. Legume 10–15 cm long × 4–5 cm wide × 1–2 cm thick, fulvous strigose, laterally compressed, pedicel attached below the dorsal suture. Seeds 2.5–3 cm long × 2.5–3 cm wide × 1–1.5 cm thick, subcubic, black, smooth.</p><p>Etymology. The specific epithet comes from the Latin word hirsutus, meaning “rough”, “shaggy”, or “bristly”, and refers to the indumentum of the calyx in this species.</p><p>Distribution and habitat. This species is known only from Papua New Guinea, where it occurs in humid and riverine forests (Fig. 3C).</p><p>Preliminary conservation assessment. This species is only known from four collections. Based on these specimens, the Extent of Occurrence is estimated as 3,909 km ² and the Area of Occupancy (AOO) as 16 km ², both falling within thresholds for a threatened category under criteria B1 and B2 respectively. However, much of this species’ range has not been intensively explored by botanists and it is possible that this species is much more widespread, in which case the EOO and AOO could be much larger. Two collecting localities are in areas where native vegetation appears to be intact, whereas the remaining two are in areas which appear to be largely deforested as a result of agricultural and settlement expansion. This species has been collected both from highlands, which have relatively low levels of deforestation, as well as coastal areas where habitat loss is more substantial. Given that the overall distribution of this species is highly uncertain, it is difficult to determine if this species is undergoing a continuing decline across most of its range. It is not likely to be severely fragmented or subject to extreme fluctuations. We propose its classification as Data Deficient (DD) following the IUCN (2024) criteria.</p><p>Comments. Macropsychanthus hirsutus is easily distinguished by its fulvous, erect trichomes on stems, inflorescences and flower buds. This is the only Southeast Asian species in the genus known to have black, cubic seeds.</p><p>Specimens examined. PAPUA NEW GUINEA, eastern Papua, January 1941, Shaw s.n. (SING-0267295); Strickland River, 1886, Mueller s.n. (MEL-81599); Milne Bay, M.I road to Mt. Suckling, Rabaraba, 9° 62′ S, 149° 17′ E, 15 June 1972, Katik 46985 (BRI, GH, L, NSW, SING, US); Milne Bay, North slopes of Mt. Dayman, Maneau Range, 27 July 1953, Brass 23479 (CAN, L, BUS); Morobe, Bumbu river near Lae, 6° 75′ S, 149°17′ E, August 1961, Millar 13819 (CANB, E, GH, K, L, NSW); Morobe, Bumbu river near Lae, 6° 75′ S, 147° 17′ E, 7 November 1961, Millar 13855 (CANB, GH, K, L, NSW); Morobe, Eastern slope of Adzare Range, Bumbu River, east of Lae, 6° 75′ S, 147º E, 29 August 1964, Royen 20061 (BRI, L).</p></div>	https://treatment.plazi.org/id/344687B4FFA7FE44FF383B83FD2F6DA4	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Fonseca-Cortés, Andrés;Clark, Ruth P.;Snak, Cristiane;Queiroz, Luciano Paganucci De	Fonseca-Cortés, Andrés, Clark, Ruth P., Snak, Cristiane, Queiroz, Luciano Paganucci De (2025): A Taxonomic Revision of Macropsychanthus (Leguminosae-Papilionoideae) Reveals New Species and New Circumscriptions in Southeast Asia and Oceania. Phytotaxa 720 (2): 93-120, DOI: 10.11646/phytotaxa.720.2.1, URL: https://doi.org/10.11646/phytotaxa.720.2.1
344687B4FFA6FE42FF383EACFBE9680C.text	344687B4FFA6FE42FF383EACFBE9680C.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Macropsychanthus lauterbachii Harms. A. Leaf B. Stipule C. Inflorescence D. Flower 1900	<div><p>9) Macropsychanthus lauterbachii Harms in Schumann &amp; Lauterb., Fl. Schutzgeb. Südsee 367. 1900.</p><p>Type. Papua New Guinea, Nurufluss, 7 June 1896, Lauterbach s.n. (lectotype, designated by Queiroz &amp; Snak 2020: WRSL-064264!) . Fig. 12.</p><p>Diagnostic description. Lianas, glabrescent. Leaflets with smooth surfaces and 8–12 pairs of secondary veins. Flower buds with canescent or fulvous, sericeous indumentum. Flowers 5–7 cm long, calyx with four lobes, ten fertile stamens. Legume 16–17 cm long × 4–5 cm wide × 1–2 cm thick, fulvous strigose, laterally compressed, pedicel attached below the dorsal suture. Seeds 2.5–3 cm long × 2.5–3 cm wide × 1.0– 1.5 cm thick, D-shaped or orbicular in outline, black, smooth.</p><p>Etymology. The specific epithet honors the German botanist Carl Adolf Georg Lauterbach, who was the first to collect this species.</p><p>Distribution and habitat. This species is known only from Papua New Guinea, where it occurs in humid and riverine forests (Fig. 3D).</p><p>Preliminary conservation assessment. The Extent of Occurrence (EOO) is estimated as 158,048 km 2, which greatly exceeds thresholds for a threatened category under criterion B1. Based on herbarium specimen records, the Area of Occupancy (AOO) is estimated as 24 km ². The AOO is likely an underestimate given that botanical collection efforts have been limited in some parts of this species’ range, however it is considered unlikely that the true value exceeds the threshold for a threatened category under criterion B2. It is only known from six locations: most of these are from lowland areas which are threatened by agricultural and settlement expansion and as such, the species is inferred to be undergoing a continuing decline in the area, extent, and quality of habitat. However, the species has also been collected from the interior of Papua New Guinea, where natural habitats are largely intact and botanical sampling efforts have been low. While the species may be more widespread than is currently known, we take a precautionary approach and propose classifying this species as Vulnerable B2ab(iii), following the IUCN (2024) criteria.</p><p>Comments. Macropsychanthus lauterbachii is similar to M. glabricalyx due to its glabrous stems and leaflets. However, the two species can be readily distinguished by their leaflet venation and calyx indumentum. Macropsychanthus lauterbachii has leaflets with 8–11 pairs of secondary veins and a calyx covered in sericeous indumentum, which may be fulvous or canescent. In contrast, M. glabricalyx has leaflets with 6–8 pairs of secondary veins and a glabrous calyx.</p><p>Specimens examined. PAPUA NEW GUINEA, 6 Jun 1896, Lauterbach 2251 (WRSL, K); Fly River, 528 Mile Camp., May 1936, Brass 6738 (GH, BRI, L); Central, Varirata National Park at c. 100 m on Varirata Lookout trail, 9° 45′ S, 147 37º E, 1 Oct 1992, Hopkins 1360 (K); Central, Koitaki, 19 April 1935, Carr 11936 (L, SING); Central Division, Dieni, Ononge road, April–May 1933, Brass 3856 (BRI, GH); Chimbu, Crater Mt. Wildlife Management Area, E of Haia village; hill forest with some anthropogenic disturbance, 6° 72′ S, 145º E, 18 March 1997, Takeuchi 11839 (AAH, CANB, K, L, NSW, US); Madang, new logging road area that was being bulldozed off of logging Rd. 7, Gogol Valley Woodchip Project area. Subprovince Madang, 5° 25′ S, 145° 62′ E, 25 April 79, Sohmer 75175 (AAH, E, BRI, CANB, Madang, Wedegumav Conservation area, Urumarav, Bogia dist., 4° 35′ S, 145° 1′ E, 16 May 2005, Kuria 87168 (K, L); New Britain, Talasea, 5° 6′ S, 150° 42′ E, April 1959, White 10909 (BRI).</p></div>	https://treatment.plazi.org/id/344687B4FFA6FE42FF383EACFBE9680C	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Fonseca-Cortés, Andrés;Clark, Ruth P.;Snak, Cristiane;Queiroz, Luciano Paganucci De	Fonseca-Cortés, Andrés, Clark, Ruth P., Snak, Cristiane, Queiroz, Luciano Paganucci De (2025): A Taxonomic Revision of Macropsychanthus (Leguminosae-Papilionoideae) Reveals New Species and New Circumscriptions in Southeast Asia and Oceania. Phytotaxa 720 (2): 93-120, DOI: 10.11646/phytotaxa.720.2.1, URL: https://doi.org/10.11646/phytotaxa.720.2.1
344687B4FFA0FE41FF383B54FCC46AA0.text	344687B4FFA0FE41FF383B54FCC46AA0.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Macropsychanthus purpureus (Elmer) L. P. Queiroz & Snak	<div><p>10) Macropsychanthus purpureus (Elmer) L.P. Queiroz &amp; Snak</p><p>Luzonia purpurea Elmer, Leafl. Philipp. Bot. 1: 220. 1907.</p><p>Type: Philippines, Luzon, Province of Tayabas, Lucban, May 1907, Elmer 9013 (holotype: PNH; isotypes: A-00057462!, E-00301634!, L-0019058!, MO-256507!, NY-00016167!, US-00004668!) . Fig. 13.</p><p>Diagnostic description. Lianas, glabrescent. Leaflets with smooth surfaces and 7–10 pairs of secondary veins. Flowers 2–2.7 cm long, calyx with two lobes, five fertile stamens and five staminodes. Legume and seeds unknown.</p><p>Etymology. The specific epithet comes from the Greek word πορφύρεος (porphúreos), meaning “purple”, referring to the color of the flowers.</p><p>Distribution and habitat. Macropsychanthus purpureus is known only from the Philippines, where it occurs in humid forests (Fig. 2D).</p><p>Preliminary conservation assessment. The Extent of Occurrence (EOO) is estimated as 77,384 km 2, which exceeds thresholds for a threatened category under criterion B1. Based on herbarium specimen records, the Area of Occupancy (AOO) is estimated as 20 km ². The AOO is likely an underestimate given that botanical collection efforts have been limited in some parts of this species’ range, however it is considered unlikely that the true value exceeds the threshold for a threatened category under criterion B2. It is only known from five locations, with no new collections since 1993. It is inferred to be undergoing a continuing decline in the area and quality of its habitat due to deforestation associated with urbanization, palm oil plantations, and agricultural expansion. Considering these factors, we propose classifying this species as Endangered B2ab(iii), following the IUCN (2024) criteria.</p><p>Comments. Macropsychanthus purpureus can be confused with M. hexander and M. wilsonii due to similar number of secondary veins in their leaflets. However, M. purpureus is characterized by its basifixed triangular stipules (in contrast to the lanceolate medifixed stipules found in the other species) and its minute stipels, which are barely visible to the naked eye (versus clearly visible stipels in M. hexander and M. wilsonii). Furthermore, M. purpureus is the only species of the genus with bilabiate flower calyx, differing from the four- or five-lobed calyx observed in the other species. Additionally, the keel of M. purpureus measures 20–25 mm in length, whereas in M. hexander and M. wilsonii the keel ranges from 10 to 18 mm long.</p><p>Specimens examined. PHILIPPINES, Leyte, 30 Aug 1915, Wenzel 1595 (US); Luzon, Bayninan, Banaue, Ifugao forest, 6 July 1963, Conklin &amp; Buwaya 80687 (L); Luzon, Malieboi, Tayabas, April 1903, Elmer 2446 (K); Luzon, Aurora Prov., on road Baler-Palayan, km 22–23 from San Luis, 15° 67′ N, 121° 47′ E, 14 June 1993, Soejarto 7967 (US, L); Luzon, Lamao river, Mt. Mariveles Province of Batan, May 1904, Borden 3050 (US); Tayabas, Lucban, Island Luzon, May 1907, Elmer 9013 (GH, MO, NY, US, VT).</p></div>	https://treatment.plazi.org/id/344687B4FFA0FE41FF383B54FCC46AA0	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Fonseca-Cortés, Andrés;Clark, Ruth P.;Snak, Cristiane;Queiroz, Luciano Paganucci De	Fonseca-Cortés, Andrés, Clark, Ruth P., Snak, Cristiane, Queiroz, Luciano Paganucci De (2025): A Taxonomic Revision of Macropsychanthus (Leguminosae-Papilionoideae) Reveals New Species and New Circumscriptions in Southeast Asia and Oceania. Phytotaxa 720 (2): 93-120, DOI: 10.11646/phytotaxa.720.2.1, URL: https://doi.org/10.11646/phytotaxa.720.2.1
344687B4FFA3FE40FF3839A0FBEC6860.text	344687B4FFA3FE40FF3839A0FBEC6860.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Macropsychanthus umbrinus (Elmer) L. P. Queiroz & Snak, PhytoKeys	<div><p>11) Macropsychanthus umbrinus (Elmer) L.P. Queiroz &amp; Snak, PhytoKeys 164: 104, 2020.</p><p>Dioclea umbrina Elmer, Leafl. Philipp. Bot. 1: 224. 1907.</p><p>Type: Philippines, Leyte, January 1906, Elmer 7249 (holotype: PHN; isotype: K-000898375!) . Fig. 14.</p><p>Diagnostic description. Lianas with fulvous indumentum overall, and canescent indumentum on the inflorescence. Leaflets with smooth surfaces and 8–11 pairs of secondary veins. Flowers 1–1.5 cm long, calyx with four lobes, ten fertile stamens. Legume 10–12 cm long × 4–4.5 cm wide × 1.5–2 cm thick, fulvous villose, laterally compressed, pedicel attachment displaced toward the dorsal suture. Seeds 2–2.5 cm long × 1.5–2 cm wide × 1–1.5 cm thick, orbicular in outline, brown, smooth.</p><p>Etymology. The specific epithet derives from the Middle French word “umbre” meaning “brown”, likely referring to the color of the fruit indumentum.</p><p>Distribution and habitat. Macropsychanthus umbrinus is endemic from the Philippines, where it occurs in humid and riverine forests (Fig. 2E).</p><p>Preliminary conservation assessment. The Extent of Occurrence (EOO) is estimated as 639,904 km ², which greatly exceeds thresholds for a threatened category under criterion B1. The Area of Occupancy (AOO) is estimated as 56 km ², which meets the threshold for Endangered (EN) under criterion B2 (AOO &lt;500 km ²). The species is threatened by deforestation due to logging, shifting agriculture, and clearance for settlements (Curtis et al., 2018, Wikramanayake 2025). This threat is inferred to be contributing to a continuing decline in the area and quality of habitat for this species. It is known from 14 locations, barely exceeding the threshold for a threatened category. Since this species nearly meets all of the subcriteria for a threatened category under criterion B2, but occurs at more than 10 locations, we propose classifying this species as Near Threatened B2ab(iii) according to IUCN criteria (2024).</p><p>Comments. This species could be confused with M. hexander due to similarities in leaflet morphology, shared indumentum type, and the number of secondary veins. However, M. umbrinus can be distinguished by its canescent indumentum on the inflorescences, smaller flowers (1–1.5 cm long), ten fertile stamens, villose pods, and orbicular in outline seeds. In contrast, M. hexander has fulvous indumentum on the inflorescences, larger flowers (2–2.5 cm long), six fertile stamens and four staminodes, strigose pods, and laterally compressed, D-shaped seeds.</p><p>Specimens examined. PHILIPPINES, Laguna, Los baños (Mt. Maquiling). Island of Luzon, June–July 1917, Elmer 17865 (US, P, L, U); Leyte, Palo, Leyte, 1828, Elmer 7249 (K); Luzon, San Mariano, Isabela province, February– March 1926, Ramos &amp; Edaño 46734 (P); Luzon, Manille, w.d., Cumming 521 (P); Luzon, Batigui Promontory, Batangas Province (S.E.), December 1950, Sulit 13832 (L); Luzon, Bapuio, Mar 1907, Elmer 8922 (K); Luzon, Calauan, prov. of Laguna, November–December 1910, McGregor 12394 (K); Luzon, Antipolo, Province of Rizal, November 1914, Ramos 22257 (K, L, US); Luzon, Antipolo, Prov. Rizal, March 1903, Elmer 1621 (US); Luzon, Province of Rizal, January 1911, Ramos 708 (US, U, SI, U); Mindanao, Todaya (mt. Apo), District of Davao, October 1909, Elmer 11905 (L, U, US, WRSL); Mindoro, Naujan, November–December 1925, Ramos 46455 (P); Palawan, Silanga, May 1913, Merrill 9595 (US, K); Palawan, Balabac Island, November 1927, Ramos &amp; Edaño 49804 (BR); Panay, Jamindan, Capiz province, April–May 1918, Ramos &amp; Edaño 31387 (US, P); Samar, Catubig river, February–March 1916, Ramos 24168 (US); THAILAND. Chonburi, Si Racha, 20 December 1907, Collins 1821 (US).</p></div>	https://treatment.plazi.org/id/344687B4FFA3FE40FF3839A0FBEC6860	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Fonseca-Cortés, Andrés;Clark, Ruth P.;Snak, Cristiane;Queiroz, Luciano Paganucci De	Fonseca-Cortés, Andrés, Clark, Ruth P., Snak, Cristiane, Queiroz, Luciano Paganucci De (2025): A Taxonomic Revision of Macropsychanthus (Leguminosae-Papilionoideae) Reveals New Species and New Circumscriptions in Southeast Asia and Oceania. Phytotaxa 720 (2): 93-120, DOI: 10.11646/phytotaxa.720.2.1, URL: https://doi.org/10.11646/phytotaxa.720.2.1
344687B4FFA2FE4EFF383D32FE3D6AA0.text	344687B4FFA2FE4EFF383D32FE3D6AA0.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Macropsychanthus wilsonii (Standl.) L. P. Queiroz & Snak, PhytoKeys	<div><p>12) Macropsychanthus wilsonii (Standl.) L.P. Queiroz &amp; Snak, PhytoKeys 164: 105, 2020.</p><p>Dioclea wilsonii Standl., Publ. Field Mus. Nat. Hist., Bot. Ser. 4(8): 310–311. 1929.</p><p>Type: Honduras, 2 June 1903, Wilson 336 (holotype: F-0059180!; isotypes: NY-00007718!, US-00004644!) . Fig. 15.</p><p>Dioclea atropurpurea Pittier, Bol. Tecn. Minist. Agric. 5: 79, f. 34, 1944. Type: Venezuela, Sucre, entre Cumaná y Cumanacoa, Apr 1942, Pittier 14660 (holotype: VEN [4439]; isotypes: K-000502895!, S-R-9702!).</p><p>Diagnostic description. Lianas with dark ferruginous indumentum. Leaflets with smooth surfaces and 8–10 pairs of secondary veins. Flowers 1–1.5 cm long, calyx with four lobes, five fertile stamens and five staminodes. Legume 6–11 cm long × 5–6 cm wide × 3–4 cm thick, dark pubescent to strigose, laterally compressed, pedicel attachment displaced toward the dorsal suture. Seeds 1–4, 25–30 mm long, 15–25 mm wide, 10–15 mm thick, D-shaped or subcubic, testa dark orange, smooth, usually mottled with black spots.</p><p>Etymology. The specific epithet commemorates the American botanist Percy Wilson, who collected the type specimen.</p><p>Distribution and habitat. Macropsychanthus wilsonii is a widely distributed species found in Belize, Brazil, Colombia, Costa Rica, French Polynesia, Honduras, the Hawaiian Islands, Madagascar, Mexico, Nicaragua, Nigeria (Oladunmoye &amp; Kehinde 2011), Panama, and Samoa. It primarily inhabits coastal areas and the edges of forests (Fig. 2F).</p><p>Preliminary conservation assessment. The Extent of Occurrence (EOO) is estimated as 100,056,497 km 2, which greatly exceeds thresholds for a threatened category under criterion B1. The Area of Occupancy (AOO) is estimated as 372 km 2. which would meet the threshold for Endangered (EN) under criterion B2. However, the AOO should be considered a minimum estimate since botanical collection efforts have been limited in some parts of this species’ range. The species is neither severely fragmented nor undergoing a continuous decline. This is supported by its ability to thrive in secondary vegetation. Additionally, the species is known from many more than ten locations and has a wide distribution. Taking these factors into account, we propose classifying this species as Least Concern (LC), following IUCN (2024) criteria.</p><p>Comments. Macropsychanthus wilsonii is distinguished by its dark ferruginous indumentum, small flowers (1– 1.5 cm long), and five fertile stamens, a combination of characteristics that is unique among Southeast Asian species. It may be confused with M. hexander and M. umbrinus due to the similar leaflet morphology. However, M. hexander has fulvous indumentum and larger flowers (2–2.5 cm long) with six fertile stamens, while M. umbrinus features both fulvous indumentum and canescent indumentum on the inflorescences, and flowers with ten fertile stamens.</p><p>Specimens examined. FRENCH POLYNESIA, Raivavae, 8 August 1934, St. John &amp; Fosberg 16061 (K); Tubuai, Taahuaia, 20 August 1934, St. John 16450 (K). SAMOA, Tutuila, growing near the beacon atop Mt. Tau, 3 May 2001, Whistler 11502 (K); UNITED STATES OF AMERICA, Hawaii, Kauai, 5 October 1916, Forbes 496 (K); Hawaii, S Hilo District, near Waiakea Stream, 19 7º N, 155 7º W, 31 Jul 2001, Oppenheimer 70140 (K); Hawaii, Hamakua coast, above Onomea Bay along the old scenic drive, just below the Carlsmith residence., 9 January 1991, Herbst &amp; Staples 9277 (K); Hawaii, Kauai, Hanalei District. Waipa ahupuaà SW of Waipa stream, 2 December 1988, Flymm &amp; Hume 3221 (K).</p></div>	https://treatment.plazi.org/id/344687B4FFA2FE4EFF383D32FE3D6AA0	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Fonseca-Cortés, Andrés;Clark, Ruth P.;Snak, Cristiane;Queiroz, Luciano Paganucci De	Fonseca-Cortés, Andrés, Clark, Ruth P., Snak, Cristiane, Queiroz, Luciano Paganucci De (2025): A Taxonomic Revision of Macropsychanthus (Leguminosae-Papilionoideae) Reveals New Species and New Circumscriptions in Southeast Asia and Oceania. Phytotaxa 720 (2): 93-120, DOI: 10.11646/phytotaxa.720.2.1, URL: https://doi.org/10.11646/phytotaxa.720.2.1
