identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
03B187B0FFC6B66C2BD6FE6FA2EABA19.text	03B187B0FFC6B66C2BD6FE6FA2EABA19.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Dalbergia lanceolaria Linnaeus f. 1782	<div><p>1. Dalbergia lanceolaria Linnaeus f. (1782: 316) . Figs. 1 &amp; 3A–B.</p><p>TYPE:—CEYLON [SRI LANKA]. Koenig s. n. [BM (barcode BM000958685!)] .</p><p>For heterotypic synonyms of this species, see Li (2017: 159).</p><p>Description: —Trees, 15–20 m tall. Bark flaking. Stipules thin, subfalcate to lanceolate, 1–1.4 cm, caducous. Leaves imparipinnate, 10–25 cm; petiole 1–3 cm; rachis 9–12 cm, sparsely pubescent when young, becoming glabrous with age; leaflets (7–)9–19, thinly chartaceous, elliptic-oblong to obovate or sometimes orbicular, 1.8–5(–6) × 1–2.8(–3) cm, base attenuate, cuneate to broadly cuneate (usually asymmetrical in lateral leaflets), apex rounded to retuse; both surfaces sparsely pubescent with appressed hairs when young, becoming glabrous; secondary veins 8–10 pairs; these and reticulation coarse and prominent on both surfaces; petiolule 3–5(–7) mm. Inflorescence an axillary (or, not observed from Chinese specimens, terminal) panicle, (5–)5.5–10(–18) cm long, with flowers laxly arranged; axes and pedicel moderately pilose with pale yellow-brown hairs. Pedicel 1.5–2 mm, articulated sub-apically; bracteoles lanceolate, minute, caducous. Calyx campanulate, puberulent, with pubescence denser along margins; tube ca. 2 mm long; lobes 5, the lowest longest, lanceolate, the upper two connate. Corolla purplish; standard ovate, retuse at apex, 6–8 mm × 6–8 mm, reflexed, with a claw ca. 1 mm long; wings broadly ovate, ca. 6 × 3.5 mm, with a claw ca. 2 mm long, inner side with a downward auricle; keel semi-lunate, ca. 4 × 2.5 mm, with a claw ca. 2 mm long, inner side with a downward auricle. Stamens 10, diadelphous (5+5), with the upper ⅓ of filaments free, unequal in length (long and short ones alternating). Ovary shortly stipitate, pubescent on stipe and along sutures, 3–4-ovuled; style slender, curved; stigma minute. Pods oblong-lanceolate, 5–12.5 × 1–2.5 cm, attenuate into a stipe ca. 1 cm long at base, acute to slightly obtuse at apex, sometimes constricted between seeds; valves coriaceous, glabrous, reticulate, thickened around seeds with prominent reticulation. Seeds 1–2(–4), reniform, flattened, separating from the inner surface of the seed chamber at maturity.</p><p>Phenology: —Flowering from April to May; fruiting from November to December.</p><p>Distribution and ecology: —As the type species of the genus Dalbergia, D. lanceolaria has a wide distribution, ranging from the Indian Subcontinent to the Indochina Peninsula (Li 2017). This study represents the first record of D. lanceolaria in China, currently known only from southern Yunnan Province. The species is typically found in or near limestone mountainous regions.</p><p>Chinese vernacular name: —fi‼vnḛ/fiŀ(ă)vñḛ (pī zhēn guǒ huáng tán, ㄆ– ㄓㄣ ㄍㄨㄛˇ ㄏㄨㄤ ˊ ㄊㄢˊ). The first part “fi‼v/fiŀ(ă)v” is derived from the specific epithet lanceolaria, referring to the usually lanceolate pods of Dalbergia lanceolaria, while “nḛ/ñḛ” is the common Chinese name for the genus Dalbergia .</p><p>The Chinese name of D. lanceolaria was originally given as “fi‼叶nḛ/fiŀ(ă)ĸñḛ” by Li (2017), where the first part “fi‼叶/fiŀ(ă)ĸ” means “lanceolate leaf/leaflet”. This name is inappropriate since the species usually does not have lanceolate leaflets.</p><p>Conservation status: —Following the IUCN Red List Standards and Petitions Subcommittee (2024), Dalbergia lanceolaria is assessed as Least Concern (LC) due to its wide distribution and relatively common occurrence in Xishuangbanna Prefecture.</p><p>Taxonomic remarks: —Among Chinese species of Dalbergia, D. lanceolaria is most closely related to D. assamica Bentham (in Miquel 1852: 256), with very subtle morphological differences between them. These subtle distinctions led Thothathri (1983 [1985], 1987) to reduce the latter to a variety of D. lanceolaria subsp. lanceolaria, as var. assamica (Benth.) Thothathri (1983: 171) . According to Niyomdham (2002), D. lanceolaria can be distinguished from D. assamica by its coarse and prominent secondary veins and reticulation on both surfaces of mature leaflets when dry (vs. thin and fine secondary veins and reticulation, rather obscure on abaxial surface when dry in D. assamica). It can be also distinguished from D. assamica by its flanking bark (vs. longitudinally fissured, cf. Dholariya et al. 2019) Additionally, our observations reveal that mature seeds of D. lanceolaria separate from the inner surface of the pod's seed chamber, causing them to rattle when the ripe pods are shaken. In contrast, mature seeds of D. assamica remain firmly attached to the inner wall of the pod's seed chamber and do not rattle when shaken.</p><p>Specimens examined:— CHINA. Yunnan: Xishuangbanna, Mengla, Menglun, G219, along roadsides, on slopes with limestone bedrock, alt. 677.35 m, 19 April 2024, K. Chiang KC1528 (IBSC, NPH, PE). Mengla, Yiwu, Menghuyanzi, on slopes with limestone bedrock, alt. 825.86 m, 19 April 2024, S. J. Li 5582 (NPH). ibid., alt. 992.37 m, ead. die, S. J. Li 5583 (NPH). ibid., besides villages, ead. die, S. J. Li 5584 (NPH). ibid., ead. die, S. J. Li 5584bis (NPH).</p></div>	https://treatment.plazi.org/id/03B187B0FFC6B66C2BD6FE6FA2EABA19	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	Dong, Jin-Long;Jiang, Kai-Wen;Biao, A.;Shu, Nan;Huang, Hui-Wen;Song, Zhu-Qiu;Pan, Bo;Tu, Tie-Yao;Li, Shi-Jin	Dong, Jin-Long, Jiang, Kai-Wen, Biao, A., Shu, Nan, Huang, Hui-Wen, Song, Zhu-Qiu, Pan, Bo, Tu, Tie-Yao, Li, Shi-Jin (2025): Three new recorded species of the genus Dalbergia (Fabaceae: Papilionoideae: Dalbergieae) from southwestern China. Phytotaxa 720 (2): 140-148, DOI: 10.11646/phytotaxa.720.2.4, URL: https://doi.org/10.11646/phytotaxa.720.2.4
03B187B0FFC5B66A2BD6FAC3A3B2B9E1.text	03B187B0FFC5B66A2BD6FAC3A3B2B9E1.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Dalbergia nigrescens Kurz 1875	<div><p>2. Dalbergia nigrescens Kurz (1875: App. A: 48 &amp; App. B: 45). Figs. 2 &amp; 3C.</p><p>TYPE:— MYANMAR, Pegu, R. Wright 926 [holotype K (barcode K000264335!), isotype K (barcode K000264336!) .</p><p>For heterotypic synonyms of this species, see Li (2017: 188).</p><p>Description: —Trees, up to 20(–30) m tall. Young branches puberulent. Stipules caducous. Leaves imparipinnate, 10–20 cm; petiole 2–3 cm, rachis 8–10 cm, puberulent; leaflets 9–15, thinly chartaceous, alternate, ovate, obovateoblong to oblong, 2.5–4.5 × 1.5–2 cm, base rounded to obtuse, apex rounded to retuse or less frequently obtuse; adaxial surface glabrous, abaxial surface puberulent to almost glabrous; secondary veins 7–9 pairs, prominent adaxially, slightly prominent abaxially; reticulation slightly prominent adaxially, obscure abaxially; petiolule 2–3 mm. Inflorescence a panicle, terminal or axillary, (3–) 5–10 cm; axes and pedicels pubescent with yellowish-brown hairs, becoming glabrous when fruiting; pedicel 1.5–2 mm, articulated sub-apically; bracteoles caducous. Calyx campanulate; tube ca. 2 mm; lobes 5, the lowest longest, lanceolate. Corolla white with blue stripes; standard narrowly obovate, emarginate at apex, ca. 4.5 × 3 mm, dorsally curved, with a claw ca. 2 mm; wings oblong, ca. 5 × 2 mm, auriculate, with a claw ca. 2 mm; keel semi-lunate, ca. 3.5 × 2 mm, with a claw ca. 2 mm, auriculate. Stamens 10, diadelphous (5+5), with the upper ⅓ of filaments free, equal in length. Ovary stipitate, pubescent along sutures, 2–3(–4)-ovuled; style slender, stigma slightly expanded. Pods oblong, (4–)4.5–8.5 × (0.8–)1–1.4(–2.5) cm, dark brown to black, attenuate to a stipe 0.4–0.7 cm long at base, apex obtuse, rounded to acute, sometimes shortly rostrate; valves coriaceous, reticulation inconspicuous, thickened and raised around seeds. Seeds 1–2, reniform, flattened, ca. 9.5 × 6.5 mm, dark brown to black.</p><p>Phenology: —Flowering from March to May (cf. Li 2017); fruiting from May to August.</p><p>Distribution and ecology: — Dalbergia nigrescens is known from the southern Indian Subcontinent and southern Indochina Peninsula (Myanmar, Thailand, Laos, Vietnam, and Cambodia; Li 2017). This species is reported here for the first time from China, currently known only from Yingjiang County, Yunnan Province, which borders Myanmar. It grows along roadsides in tropical evergreen forests.</p><p>Chinese vernacular name: —ā叶nḛ/āĸñḛ (hēi yè huáng tán, ㄏㄟ –ㄝˋ ㄏㄨㄤˊ ㄊㄢˊ, cf. Li 2017). The first part “ā叶/āĸ” is derived from the specific epithet nigrescens, referring to the leaflets of Dalbergia nigrescens turns black or dark brown when dry.</p><p>Conservation status: —Since we examined only one collection of Dalbergia nigrescens from China made by one of us (see Specimens examined below), we follow Barstow (2001) in assessing the species as Data Deficient (DD).</p><p>Taxonomic remarks: —(1) The description of inflorescence and flowers, as well as the phenology given below, are based mainly on Li (2017), as we examined only one fruiting collection.</p><p>(2) While previous literature (Li 2017) documented that Dalbergia nigrescens could be characterized by leaflets that turn dark brown to black when dried, our recent observations suggest that this darkening is largely attributable to specimen processing conditions. When dried rapidly using a drying oven (approximately 60°C), specimens may retain their green coloration. Although this character may be useful to some degree, caution should be exercised when relying on it as a distinguishing feature.</p><p>Based on further observations, D. nigrescens can be distinguished from related species by several pod characteristics. It differs from D. assamica by having pod valves that are obviously thickened and raised around seeds (vs. not or slightly thickened and raised around seeds). It can be separated from D. lanceolaria by the inconspicuously reticulated thickened portions of the valves (vs. obviously reticulated). Finally, it differs from D. oliveri by its generally shorter pods [(4–)4.5–8.5 vs. 9–11(–14) cm] combined with inconspicuously reticulated thickened valve portions (vs. reticulation absent). Nevertheless, the relationships among these four species require further investigation.</p><p>Specimens examined:— CHINA. Yunnan: Dehong, Yingjiang, along roadsides, 15 August 2020, Z. Q. Song 202023 (IBSC, NPH).</p></div>	https://treatment.plazi.org/id/03B187B0FFC5B66A2BD6FAC3A3B2B9E1	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	Dong, Jin-Long;Jiang, Kai-Wen;Biao, A.;Shu, Nan;Huang, Hui-Wen;Song, Zhu-Qiu;Pan, Bo;Tu, Tie-Yao;Li, Shi-Jin	Dong, Jin-Long, Jiang, Kai-Wen, Biao, A., Shu, Nan, Huang, Hui-Wen, Song, Zhu-Qiu, Pan, Bo, Tu, Tie-Yao, Li, Shi-Jin (2025): Three new recorded species of the genus Dalbergia (Fabaceae: Papilionoideae: Dalbergieae) from southwestern China. Phytotaxa 720 (2): 140-148, DOI: 10.11646/phytotaxa.720.2.4, URL: https://doi.org/10.11646/phytotaxa.720.2.4
03B187B0FFC3B6682BD6FD5CA044BA3D.text	03B187B0FFC3B6682BD6FD5CA044BA3D.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Dalbergia oliveri Prain 1897	<div><p>3. Dalbergia oliveri Gamble ex Prain (1897: 451) . Fig. 3D.</p><p>TYPE:— UPPER BURMA [MYANMAR]. Wuntho, February 1892, J. W. Oliver s. n. [lectotype CAL (barcode CAL0000015279!), designated by Thothathri (1987: 134), isolectotype K (barcode K000264350!) .</p><p>For heterotypic synonyms of this species, see Li (2017: 199).</p><p>Description: —Trees medium to large, up to 15–30 m tall. Young branches glabrous or occasionally puberulent. Stipules small, readily caducous. Leaves imparipinnate, 15–25 cm; petiole 1–3 cm; rachis 6.5–11 cm, glabrous; leaflets 7–17, alternate, chartaceous to subcoriaceous, ovate-oblong to ovate-lanceolate, 1.4–4(–8) × 0.9–2.4(–3) cm, base rounded to broadly cuneate, apex obtuse or acute with an obtuse to retuse tip, both surfaces glabrous; secondary veins 9–12 pairs, slightly prominent on both surfaces, reticulation ± obvious; petiolule (3–) 4–7 mm. Inflorescence a panicle, axillary and subterminal, or terminal (not observed in Chinese specimens), 4–10.5(–15) cm, flowers laxly arranged; axes and pedicels puberulent with rusty hairs when young (not observed in Chinese specimens), becoming glabrous in fruit. Pedicels 2–3 mm long; bracteoles small, readily caducous. Calyx campanulate; tube ca. 2.5 mm long, puberulent with rusty hairs; lobes 5, the lowest lanceolate and longest. Corolla purplish; standard suborbicular, ca. 7 × 7 mm, retuse at apex, reflexed, with a claw ca. 2 mm long; wings broadly obovate, ca. 7 × 3.5 mm, with a claw ca. 2 mm long, inner side with a downward auricle; keel semi-lunate, 5 × 2.5–3 mm, with a claw ca. 2 mm long, inner side with a downward auricle. Stamens 10, diadelphous (5+5), with the upper ⅓ of filaments free, unequal in length. Ovary stipitate, pubescent on lower part and along sutures, 3–4-ovuled; style slender, conical; stigma slightly expanded. Pods rounded-ligulate, oblong to strap-shaped, 9–11(–14) × 1.6–1.8(–4) cm, attenuate into a stipe 0.6–1 cm long at base, apex acute to acuminate or forming an elbow-tweezer-like tip (in Chinese specimens); valves coriaceous, obviously thickened and raised around seeds with reticulation absent, elsewhere with obvious reticulation extending to margins. Seeds 1–2(–3), reniform, flattened, ca. 12 × 6 mm.</p><p>Phenology: —Flowering from March to April (cf. Li 2017); fruiting from May to August.</p><p>Distribution and ecology: — Dalbergia oliveri is widely distributed in the Indochina Peninsula and was previously known only as an introduced and cultivated species in China and Malaysia (Li 2017). This species is reported here for the first time as native to China. It is currently known only from Yingjiang County, Yunnan Province, where it grows on slopes in tropical evergreen forests.</p><p>Chinese vernacular name: —中南nḛ/中南ñḛ (zhōng nán huáng tán, ㄓㄨㄥ ㄋㄢˊ ㄏㄨㄤˊ ㄊㄢˊ). The first part “中南” refers to the wide distribution of Dalbergia oliveri in Indochina Peninsular. In the Chinese timber trade, this species is also known as “奥aenḛ/奧aeñḛ (ào shì huáng tán, ㄠˋ ㄕˋ ㄏㄨㄤˊ ㄊㄢˊ)” (cf. Li 2017), in which the first part refers to the pronunciation of initial letters of specific epithet in Chinese.</p><p>Conservation status: —Although Dalbergia oliveri is widely distributed in the Indochina Peninsula, it has been heavily exploited for its valuable hardwood, which is close-grained, red-colored, and prized for furniture and ornamental work (Thothathri 1987). Its commercial value in the timber trade (Phong et al. 2011) has led to widespread deforestation and population decline. Despite reports that this species may be locally common in Yingjiang County (Bin Tian, pers. comm.), we follow Barstow et al. (2022) in assessing it as Critically Endangered (CR A2cd+3cd+4cd).</p><p>Taxonomic remarks: —(1) The description of inflorescence and flowers, as well as the phenology given below, are based mainly on Li (2017), as we examined only one fruiting collection.</p><p>(2) Among Chinese species of Dalbergia, D. oliveri is most closely related to D. lanceolaria L. f. and its allies, but can be readily distinguished from them by its pods being obviously thickened and raised around seeds without reticulation [vs. pods less prominently thickened and raised around seeds with inconspicuous to obvious reticulation, cf. Taxonomic remark (2) under D. nigrescens].</p><p>Specimens examined:— CHINA. Yunnan: Dehong, Yingjiang, along roadsides, on slopes, alt. 422 ± 3 m, 3 June 2023, N. Shu et al. KC634bis (IBSC, NPH).</p></div>	https://treatment.plazi.org/id/03B187B0FFC3B6682BD6FD5CA044BA3D	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	Dong, Jin-Long;Jiang, Kai-Wen;Biao, A.;Shu, Nan;Huang, Hui-Wen;Song, Zhu-Qiu;Pan, Bo;Tu, Tie-Yao;Li, Shi-Jin	Dong, Jin-Long, Jiang, Kai-Wen, Biao, A., Shu, Nan, Huang, Hui-Wen, Song, Zhu-Qiu, Pan, Bo, Tu, Tie-Yao, Li, Shi-Jin (2025): Three new recorded species of the genus Dalbergia (Fabaceae: Papilionoideae: Dalbergieae) from southwestern China. Phytotaxa 720 (2): 140-148, DOI: 10.11646/phytotaxa.720.2.4, URL: https://doi.org/10.11646/phytotaxa.720.2.4
03B187B0FFC1B6682BD6FE18A0A9BCD6.text	03B187B0FFC1B6682BD6FE18A0A9BCD6.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Dalbergia (sect. Dalbergia) sect. Dalbergia	<div><p>Key to Chinese species of Dalbergia sect. Dalbergia</p><p>The type species of the genus Dalbergia, D. lanceolaria L. f., and its allies comprise section Dalbergia . This section was previously known as section Dalbergaria Prain (1905 [1904]: 85). However, according to Art. 22.2 of the International Code of Nomenclature for algae, fungi, and plants (ICN; Madrid Code, Turland et al. 2025), a name of a subdivision of a genus that includes the type of the adopted, legitimate name of the genus is not validly published unless its epithet repeats the generic name unaltered. Therefore, the sectional name Dalbergaria was not validly published and should not be used; instead, the autonym sect. Dalbergia should be adopted.</p><p>This section, based on the treatments by Prain (1905 [1904]) and Thothathri (1987), as well as the species key by Li (2017), comprises ca. 16 species distributed in tropical and subtropical Asia, and has been supported as a monophyletic clade in phylogenetic studies 1,2 (Vatanparast et al. 2013, Sotuyo et al. 2022). Members of this section are characterized by their stamens in 5+5 diadelphous arrangement [except D. polyadelpha Prain (1905 [1904]: 84), stamens irregularly separated to incompletely 3–5-adelphous on upper part] and coriaceous pods. Currently, nine species of this section are known from China. A key to these species (mainly based on fruiting specimens) is provided below.</p><p>1. Climbers or scandent shrubs...............................................................................................................................................................2</p><p>-. Generally erect trees ...........................................................................................................................................................................3</p><p>2. Leaflets 15–25; panicle generally shorter than its subtending leaf; pods strongly thickened and spongy around seeds..................... ................................................................................................................................................... D. stipulacea Roxburgh (1832: 233)</p><p>-. Leaflets 9–13; panicle generally longer than its subtending leaf; pods not thickened around seeds as above .................................... ............................................................................................................................................ D. volubilis Roxburgh (1798 [1805]: 48)</p><p>3. Leaflets acute to acuminate at apex....................................................................................................................................................4</p><p>-. Leaflets rounded, obtuse to retuse at apex..........................................................................................................................................5</p><p>4. Pods glabrous except for short stipe............................................................................................................................ D. polyadelpha</p><p>-. Pods brown puberulent.................................................................................................... D. hainanensis Merrill &amp; Chun (1934: 32)</p><p>5. Pods not reticulate opposite seeds ........................................................................................................................................ D. oliveri</p><p>-. Pods ± reticulate opposite seeds .........................................................................................................................................................6</p><p>6. Pods inconspicuously reticulate opposite seeds .................................................................................................................................7</p><p>-. Pods obviously reticulate opposite seeds ...........................................................................................................................................8</p><p>7. Pods obviously thickened and raised around seeds....................................................................................................... D. nigrescens</p><p>-. Pods not or slightly thickened and raised around seeds ................................................................................................... D. assamica</p><p>8. Leaflets 7– 113; mature seeds firmly attached to the inner wall of the pod’s seed chamber .................. D. hupeana Hance (1882: 5)</p><p>-. Leaflets (7–)9–19; mature seeds separate from the inner surface of the pod’s seed chamber ..................................... D. lanceolaria</p><p>Notes: — 1 Phylogenetic analyses by Vatanparast et al. (2013) and Sotuyo et al. (2022) did not place Dalbergia sericea within the Dalbergia sect. Dalbergia clade. Upon examining the voucher specimen (BANGLADESH. Chittagong, 25 April 1994, A. M. Huq &amp; M. K. Mia 10336 [L]) used in their studies, we found it to be a misidentification. This specimen likely represents a species closely related to Dalbergia velutina Bentham (in Miquel 1852: 255), characterized by membranous pods containing elongate seeds.</p><p>2 Notably, phylogenetic analyses based on chloroplast genomes by Rather et al. (2025) placed D. obtusifolia Prain (1901 [1902]: 42) and D. mimosoides Franchet (1889: 187) within the Dalbergia sect. Dalbergia clade. However, this result may be based on misidentification of voucher specimens (vouchers not traced by the current authors) and conflicts with both morphological data (see Li 2017) and our unpublished molecular phylogenetic data. Therefore, their results are not recognized here.</p><p>3 Li (2017), in his key to species and species descriptions, stated the leaflet number of Dalbergia hupeana as 3–5. This should be corrected to 3–5-paired leaflets.</p></div>	https://treatment.plazi.org/id/03B187B0FFC1B6682BD6FE18A0A9BCD6	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	Dong, Jin-Long;Jiang, Kai-Wen;Biao, A.;Shu, Nan;Huang, Hui-Wen;Song, Zhu-Qiu;Pan, Bo;Tu, Tie-Yao;Li, Shi-Jin	Dong, Jin-Long, Jiang, Kai-Wen, Biao, A., Shu, Nan, Huang, Hui-Wen, Song, Zhu-Qiu, Pan, Bo, Tu, Tie-Yao, Li, Shi-Jin (2025): Three new recorded species of the genus Dalbergia (Fabaceae: Papilionoideae: Dalbergieae) from southwestern China. Phytotaxa 720 (2): 140-148, DOI: 10.11646/phytotaxa.720.2.4, URL: https://doi.org/10.11646/phytotaxa.720.2.4
