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BLUMEA 30 (1984) 77-87 The genus Mastersia P.C. van (Papilionaceae: Welzen &: S. den Rijksherbarium, Leiden, Phaseoleae) Hengst The Netherlands Summary Characteristic cles. Within bakeri this (Koord.) tion Backer of both pattern Mastersia species two from the indehiscent are the Phaseoleae in the and are found in the with pods M. assamica recognized: are Celebes Borneo, characters within placed is only distinctive closely related; Mastersia for the genus genus Moluccas. seeds with Benth. Both species bracteoles, wing petals, the subtribe elongated funi- from Assam and M. are keel considered petal The Glycininae-Glycinastrae. and pod. distribu- is discussed. species Introduction The genus Mastersia (Bentham, 1965b) as first was its described by based only species, on Bentham Griffith and Wallich. Bentham commemorated with this of Dr. T. Maxwell Masters. material as Bentham did and Baker's ognized assamica Baker (see Koorders thereby described M. creating mistake and sunk the latter note under the a name and with M. assamica collected in East India new genus name. by the labours name cleistocarpa, superfluous using Prain the same (1897) rec- into the synonymy of M. correctly latter). described Mucuna bakeri. Backer (1898) generic identity (1876) (1865a), specimens made the (in Heyne, 1927) combination in Mastersia. See also corrected the note 1 under M. bakeri. Harms (1911) (Borneo), neensis study present described both both two species new species: M. sarasinorum reduced are to M. bakeri MORPHOLOGICAL Leaves (Fig. la) Stipulae and lose hairs the nerves to are usually stipellae — are The leaves are present, but more (see note and M. bor- caducous. on 2 under this the and The upper pinnately leaflets side. are Hairs on uniseriate, 3-celled (Lackey, trifoliolate. pilose, on permanent. Mature leaflets of M. assamica show be earlier devoid of hairs species). NOTES spirally arranged early during maturation, especially are (Celebes) different from each other and from M. assamica. In the slightly a but veins and tendency the upper surface than leaflets of M. bakeri. The hairs 1978). BLUMEA 78 For M. bakeri small glands. nym) as Lackey These devoid of these The upper surface No. 30, also reports (I.e.) the always present, not are VOL. - of stalked and presence he as 1984. 1, does record M. unstalked, borneensis (a syno- glands. of the leaflets lacks Paraveinal stomata. mesophyll be may present (Lackey, I.e.). Inflorescence a with raceme both sides of the base covering at — In both the base; in M. bakeri Calyx most The — The species petals for sepals is the — only bracteoles opposite they are, at completely are Keel claw. more the At present, are present just are below vexillary side, overlapping only touching connate calyx the base. at and the calyx is, are The standard lacks auricles and possesses only that in M. short-clawed, The — This distinct petals a there- present in al- two small, basal bakeri is 1981), usually about petals gradual. upper after Stirton, third of all genera show Both — In M. assamica a petals are claw An upper auricle is present. margin in M. bakeri, a to are a a de- to sculp- sculpturing (Stirton, I.e.). pocket more pos- vertical Phaseoleae from just below the apex The lateral sculp- The lamellae are and in exposed a landing usually only slightly (M. bakeri). kind of as lamellate legumes usually only blade is rather but in M. assamica a have In M. bakeri one. pocket 1981). Within the partly united, the transition from as in Mastersia is of the Moluccas specimens short-clawed and Mastersia also has exceptional, sculpturing position (terminology not rare, are distinct lower Besides the lateral developed. is somewhat The in wing in M. assamica also slightly structures. only reclined turing is the Remnants of the central of the blade, they present in the upper part slightly matures. be striated. The bracteoles to appear they elongated. pollinators (Stirton, pocket. of these and veloped is (Fig. le&g) insect above one two veins standard in M. assamica is lower auricle turing brachyblasts one caducous bracts early somewhat smaller and are dorsal upper auricle and platform usually only very short-clawed. Wing distinct sess they two petal Standard callosities. or pseudoraceme: fruits. ripe sessile a These brachyblasts. of which flowers, numerous 4-lobed. The ventral lobe fore, the three in fruit. In M. assamica persistent are The inflorescence consists of — contracted into of the inflorescence small, Because of the calyx. often bear b) are dormant bud. a Bracteoles the la & which and cushion-shaped are (Fig. fascicles is often to the in M. bakeri sharp, always present near in the middle of the blade. Stamens are for more nately longer — than The vexillary and shorter (with reflection of the standard all usually persistent filament is half of their length at are the vexillary of the the base of the completely connate. pod. same free from the other 9, which In young stages the one being shorter), length. stamens but at Remnants of the are alter- the time of filaments are P. C. van Welzen & Fruit lc & (Fig. f) The fruit — and thin. Mastersia assamica has M. bakeri has wings regular, usually be black, dish both on one- S. den with The but field observations indicate yellow Seeds In (Fig. Id) is and hang vertically The seeds — in the unique few seeds show the horizontal pod. in a pod partly in (1865a) connate Taubert with the to (with which Shuteria, funicle well-developed embryo; only a young seeds in fig. lc & f). Galactiinae of the Phaseoleae. in the Galactiinae The (both Diocleinae). vexillary somewhat large, pod, winged (1964) too. Harms stamen, which (1911) supported because of the Pueraria, and staminal heavy the Pueraria- like lower followed Bentham, but raised the Galac- basically not study. traditional six the style. or Mastersia in the this (the character is made a Baudet belongs to sensu subjective). long Cajaninae Mastersia the are more con- have Glycininae usually in- pos- Bentham also have no- allies Mastersia Lackey funicles. different classification of the Phaseoleae, also based groups his are based on differences in development Glycininae-Glycinastrae (the Glycininae Diocleinae, Glycininae s.s.,Erythryninae,Ophrestiinae,and Glycininae vision and Lackey's subdivided the tribe into three subtribes, instead of His seven. In while the Diocleinae Galactiinae rather leaf anatomy and Glycininae. Bentham. The sensu only slightly nodose, or inflorescences so chromosomes, maintained Bentham's question mark, however) (1977, 1978) the former of the investigation because of the reniform seeds with elaborate primitive group with a simple style, not of contain Kennediinae). bipartite as in and the Phaseolinae. is a Bentham, 1865a). cininae within the elongated POSITION include all Galactiinae nodose the the Mastersia the Phaseoleae, a are inflorescences, Baudet The placement much staminal tube in the Diocleinae and free in the Galactiinae after of all Glycininae prominent an a from the Galactiinae in the Hutchinson (1977a &b), florescences, on the wing petal. Mastersia the with green to red- to tribal rank. Lackey dose to Dioclea and Pueraria allied Mastersia with disk, chemotaxonomy sess to be related system) (1894) placed auricle of the cept to still Mastersia in his subtribe placed his (in view and tube, the large placed light appears Mastersia). Bentham's tiinae lacking developed embryo (the larger, considered Mastersia Diocleinae differ is pod always of seeds face each other with Usually pairs abortive, are attached are SYSTEMATIC (free the small and reniform. Their are the seeds Phaseoleae, their funicle. Most seeds per Bentham state edge only, up into ir- breaking in colour from flat breadth, the upper wing along dried a and length is indehiscent and change a its to 79 black. to pod He genus Mastersia a narrow pod two-seeded parts. or The is, in proportion pods edges. Hengst: distinct Its (in Lackey's genus, because placement concept), flower of Mastersia. The was because of flowers lack of its pod traditionally the, and within the appendages seed connection within the Galactiinae on the Phaseoleae, standard, rather the (see or the also Gly- primitive wing petals do 80 BLUMEA enclose not does the the style keel sitions among the of the Glycininae, is style No. 30, much not beard. The leaflets not are the traditional concept is not 1984 1, elongated to seems be Phaseolinae, glandular with in as the nor Cajani- because of tran- enlarged concept an with Mastersia appropriate classification, most the in as dotted fully satisfactory, subtribes. Therefore Baudet's solution, in the being placed a possess Unfortunately, nae. the petals, VOL. - Glycinastrae. GEOGRAPHY The shows genus Mastersia is found in Assam Makassar Strait deep & Clayton placed (50% species (their figures 7 attention less or similar due to is occurred Mastersia deep. the via the during that glacial Ma) Mastersia cally area sides migrate not between glacial periods. also affect the embryos). A (1981) to Naga-Khasia Southeast Asiabut also be can distribution fit treatment Styracaceae Van Steenis Erroneously, from which M. a 8 Ma 20 Sunda line of islands Shelf Ma) another during dry. The easily explained, at and/or the in- this is presence as of this strait already 'since southern end, where even extensive land may table 4.1 also shows The present East to Late Pliocene Celebes and (+ distribution suggests due only pods Raven & Polhill (1981) noted the to the wetter affect the with only few relatively poor 12—3 Australia, enabling the Moluccas. The latter region is, Borneo, perhaps not of Makassar Strait possible crossing the Late Miocene to has also Borneo could have to was onwards).' Audley-Charles' established between pollinators (Mastersia drew a more migrate from Borneo into southeast Celebes to climate does with absent; indicates that Makassar Strait existed region, (1932) (1932) bakeri is origin. Dispersal its the further eastwards and Van Steenis of the for (1979) widespread plants in any pattern, the best easily (80—40 Ma), except perhaps (from Van Steenis by Bogor herbarium. when and animals was wetter not of the Makassar Strait is less well-known. Assam Compared sub-kingdom species (fig. 18). Laurasian in also shows that chain found pattern a M. bakeri. the Mid-Miocene (+ to seen, as periods shoals landplants island a 6), his group of Indo-Malesian distribution range, Cretaceous existed. Table 4.1 an the the late Pliocene during to distribution in his presumably Doandoany have allowed with misidentifications in the or Deccan-Malesian a Wallacea-ranging a Audley-Charles Eocene one species: both sides of the of Indian grasses. chorology a Mastersia bakeri itself does in both on on the 25% isochore of their map belongs distribution during vicariant The genus Mastersia itself shows to with plants peculiar Jaya Mastersia perhaps 8). two of Indonesia 2). that of this to cluded Irian is of Mastersia & is description 12a). map distribution agrees plants. area M. assamica fits into the group of they found, (belonging group latter Malesian (his the isochore of map The small a (Borneo/Celebes, Moluccas). Malesian distribution in with disjunct distribution, Panigrahi (1975) published the distribution patterns endemic a the other in (India), an geologi- extinction in climate during plants themselves, seeds with the interit may well-developed representation of legumes P. C. in Asia tropical to data exist compared to The distribution of M. & S. den as a Unfortunately, 81 palaeontological no note introduction in Java, where the enlarged by plant cover See also the f., 1964). Mastersia genus suppositions. bakeri has been is used The Hengst: Africa and America. support the above plant occasionally den Brink Welzen van or as fertilizer a under the on uses & Bakhuizen (Backer of the description van species. ACKNOWLEDGEMENTS We Leiden, marks of this for he to indebted greatly are butions to and hospitality made Rob We publication. Geesink, thankful are facilities during the reading Wessendorp prepared offered. of the A, BM, C, CAL, K, L, SAN, SING, and Mr. J. Leiden, for Prof. Dr. guidance, critics, editing US, who the excellent personal C. Kalkman manuscript. We and his also to the staff and would kindly like of the is thanked to sent material for the loan. critical re- the directors acknowledge on and contri- Rijksherbarium, Mr. C. van Laeren drawing. REFERENCES AUDLEY-CHARLES, M.G. Whitmore, Wallace's C.A. BACKER, 1927. 1981. line In: and K. Geological history plate Heyne, tectonics: De of the 24-35. of Wallace's region line. In: T. C. Oxford. nuttige planten van Nederlandsch Indie, 2nd ed., 2: 828. Buitenzorg. & R.C. BAKER, BAKHUIZEN VAN DEN J.G. 1876. J.C. BAUDET, Leguminosae. 1977. Recherches Thesis (mimeogr.). 1978. Prodrome Bot. Nat. BENTHAM, 454, G. 1865b. CLAYTON, Bull. 300, 1911. 9: HUTCHINSON, des Groningen. 2: 195. London. Papilionaceae-Phaseoleae. classification generique des Papilionaceae-Phaseoleae. Bull. Jard. Leguminosae. In: G. Bentham & J.D. Hooker, Genera plantarum 1: 451- new G. PANIGRAHI. Uber J. overzicht der 630. of some and genera species of tropical Leguminosae. Trans. Linn 1975. Computer-aided chorology of Indian grasses. Kew die Verbreitung der Leguminosen-Gattung Mastersia. In: F. Fedde, Re- 367-369. S.H. 1964. Genera of 1898. flora flowering plants Verslag van eener botanische N.O.Celebes, uit een 1: 431. Oxford. dienstreis door wetenschappelijk de en Minahasa, praktisch tevens oogpunt: eerste 439, Batavia/'s-Gravenhage. J. A. 1977a. LACKEY, 1977b. A revised its relation 1978. D. synopsis anatomy Bot. & Raven, of Phaseoleae: classification Gaz. of 139: C.G.G.J. VAN. in 87, 88. Bot. J. Linn. Phaseoleae Thesis (mimeogr.). Ames, Soc. 74: (Leguminosae: Leguminosae. 1981. The J. As. Soc. Biogeography legume systematics 1932. Plant-geography and 163-178. Papilionoideae) 1: Styracaceae of Beng. 66, the ii: and its relation to In: R. M. Polhill & 417. Leguminosae. 27-34. Kew. of Netherlands India. Bull. 212-272. 1979. Iowa. Phaseoleae (Leguminosae: Papilionoideae), 436-446. R.M. POLHILL. Advances of the tribe distribution. 1897. Some additional P.H. STEENIS, A to canavanine Leaflet taxonomy. 12: generique 1: 631. India 669-686. KOORDERS, P.H. classification of Java of British t. 34. W.D. & 29: H. RAVEN, la Flora 183-220. Description pertorium PRAIN, sur Hooker, 535. London. Soc. 25: HARMS, 1865a. J.D. Paris. d'une 48: Belg. BRINK f. 1964. Flora In: of east Malesia. Bot. J. Linn. Soc. 79: 97-178. Jard. Bot. Btzg III 82 BLUMEA C.H. STIRTON, Advances P. TAUBERT, 3: III, in 368. 1981. Petal 1894. in sculpturing 2: legume systematics Leguminosae. VOL. - A. No. 1984 1, papilionoid legumes. 771-788. In: 30, In: R.M. Polhill & P.H. Raven, Kew. & K. Engler Die Prantl, Pflanzenfamilien naturlichen Leipzig. MASTERSLA Mastersia Benth. in 25 (2 Nov. Fl. PI. Benth. & Hook, Gen. f., Taub. in 34; Allen (1964) 431; 1 t. 1865) 300, PL Oct. (19 Nat. P., Nod. Allen, Leg. & 1 E. & 1865) 535; Benth., Trans. Pfl. Fam. 3 3, 722. (1981) 422, 423, Linn. Ty - p e: Soc. Gen. (1894) 368; Hutch., M. assamica Benth. woody, to Herbaceous somewhat ribbed. arranged, pinnately leaving convex a than longer creeping trifoliolate. revolute to ultrajugal parts. times rhomboid Stipulae Stipellae to times cuspidate; lateral leaflets and veins, nerves tinct the midrib, parallel and calyx, overlapping cent, apex flowers leaflet, of which apex. Corolla Standard glabrous. usually very longer veins 1 2 or indis- either side of slightly perpendicular rowly elliptic, turing slightly slightly equal lower auricle distinct, beneath the apex ent; lateral Vexillary when in fruit. Flowers Bracts to the papilionate. Calyx upper lobe cam- anthers longitudinal short lobes. Ovary ovary to circular to keeled developed; to claw; the latter short to in middle of not petal appendaged; Disk pubescent, stigma, annular, laterally lateral or oblong, at pocket present; sculp- partly the upper dorsifixed, consisting connate introrsely free to from to just upper auricle pres- margin alternately of 10 compressed; nar- lamellate, vertically relatively long; filaments at short; base keel; claw short; upper auricle upper central part, in uniform, ellipsoid, slits. near distinctly in- glabrous slightly ovate, claw absent broadly elliptic pocket present free, to developed at the to below the 2, just cup, sericeous outside, shorter than the Keel blade exposed. filament young; lateral slightly distinctly to reclined, slightly or the to often caducous bracts auricled; basal callosities distinct; margin entire; apex rounded. Wing blade to the acroscopic nervature on often caducous. elongated, keeled, elliptic some- broadly obovate, striately nerved, pubes- than to some- acute to apical leaflet; alternately small, some- for sometimes the hairs, except nerves much to than the caducous. Bracteoles triangular, lower lobe rounded usually being larger with 2 terminal, touching dorsally, fruit; in pulvinate. Leaflets glands occasionally present; lower surface, 4-lobed, lobes imbricate, infrajugal parts retuse to devoid of usually broadly rounded, (sub)persistent side, persistent not or side basiscopic of the and 3-flowered, the to base axillary Brachyblasts brachyblasts panulate, the on acute to to spirally the apex, caducous, at base, somewhat smaller than the unstalked distinct to Pseudoracemes base. leaves mature stalked and upper surface, on nerves. the with the usually asymmetric side; upper surface of usually lobed at rarely apex Stem round plants. when young. Leaves Petiolules ovate; base slightly emarginate; margin entire; to pulvinate triangular. times former climbing or triangular Rachis scar. usually elliptic to twining or parts all short-pubescent Vegetative near the auricle. shorter and opening longer with two somewhat adnate style laterally compressed curving upwards; stigma capitate; ovules c. near 20. Pod P. C. van Welzen & pergamentaceous, linear-oblong, both side or on the dorsal sometimes with length form, of the only; with 83 longitudinal wing a whitish pair-wise with brown, fleshy layers, outer each facing seeds most on in- brown, longitudinally arranged, perpendicular blackish two Mastersia brown; endocarp with the funicles flattened, seeds with genus in dehiscent, dark exocarp usually laterally full-grown embryos; The Hengst: flat, very soft tissue. Seeds seeds pod, smooth, edge S. den the to reni- other, bearing not dark brown, inner brownish white; funicle elongated; rim aril brownish white; hilum small, round; micropyle in raised radicular lobe. slightly Embryo Distribution. Two Found in Moluccas. places, on waste (1981) on Mastersia reported wet to dry ground. nodulate to its in roots. under M. bakeri. on uses metabolites. Secondary forest secondary Nodulation. Allen & Allen note in Assam, the other in Malesia: North Borneo, one species, Celebes, Central and North See also the a radicle folded towards the micro- long a minute. pyle; plumule Ecology. with Lackey (1977b, see under records References) cana- vanine for the seeds. KEY la. Bracteoles at the in usually broad b. side vexillary lower auricle. Keel with a Bracteoles the upper on at the sharp side always to the on upper edge. M. assamica 417. Trans. Linn. Baker Hills near and s.n. each side racemes by edge. Assam a 1—3 blade; pocket Pod with pubescent. Flower up mm; dard blade a 1—2 mm 1. M. assamica at the base. transition mm broad Wing blade with from claw wing on both an in- blade; pocket to edges. Borneo cm (1865) 300, long; to 18 5—17.5 ovate, 2 J. As. Soc. (1876) 195, s.n. Beng. 66, nom. (K, L), superfl. E. India, ii (1897) — Syn- Mishmee Rachis, infrajugal part 6.5 —12( — 18) long. Stipellae (2—)5—8 by by 3.5—12.5 cm; only pubescent caducous. already long. Calyx by 11—18 by on Brachyblasts with 3—5 acumen the 0.5—1.2 6—9 mm; a mm; 10—13 at 4—5 1.5—4 mm base, (3.5—)5—7 mm long mm. cm Petio- nerves 6—12 lower surface. Pseudo- caducous. Pedicel 5.5—11 dorsally overlapping lateral lobes 7—9 34; Prain, (K), 1824; Wallich convex. cm the flowers mm t. India Assam. See note. scar bracts Br. Fl. 522 Royle 515, Upper Bracteoles broadly 25 midrib; usually and to 1f & g. Hook.f., 1.2—3(—5.5) of the 15—68 4—5.5 in long. Leaflets brachyblasts mm. Hb. Fig. Soc. in caducous, long; ultrajugal part mm in Choonpara Stipules already lules 4—6 — cleistocarpa Benth., M. — Griffith sely Pod with blade with distinct 2. M. bakeri types: the the upper gradual a Wing Moluccas 1. Mastersia assamica Benth. on at only touching distinct lower auricle. Keel with the base. at transition between claw and sometimes edge only. vexillary THE SPECIES overlapping rather middle of blade, wing TO long. mm Bracts long, to spar- by (2.8—)3—4 cup; ventral lobe 9—12 dorsal lobe 7—10 by mm; claw 1—2 short, 6.5—8 mm mm. long. Stan- Wing BLUMEA 84 Fig. 1. Mastersia arrangement 26681, e bakeri of young Kanders wing petal, x 2½ (f, (Koord.) seeds, 272). - g Tessier X ½; Backer, d. a. VOL. 30, No. Habit, x½; seed, X2½; M. assamica 204). - Benth. e. 1, b. 1984 young inflorescence, X1; wing petal, X 2½ (a, f. Pod with c, d de arrangement of c. pod Vogel 5639, young seeds, with b SAN x ½; g. P. C. blade 9—16 3—4 by 5—7 by The Hengst: Mastersia genus claw 4.5—5 mm; beneath the upper sharp; lateral pocket usually present 10.5—13.5 long. Ovary mm Pod 6—13.5 1.8—2.9 cm; by longitudinal wing Seeds 6—20, all dissected seeds without Field Flowers notes. pink on in middle Disk lobes 0.7— long, curving upwards. mm upper margin long. mm edge 1—2 only, mm broad. well-developed embryo. a red. deep to 4.5—5 long; style mm indis- sculpturing transition between claw and long; mm of blade. Staminal tube and free part of filaments 12—15 1.5 85 claw 1—3.5 mm; lower auricle distinct; mm; tinct. Keel blade 6—11 blade rather Welzen & S. den van Young pods green. Distribution. India: Assam. Plant Ecology. drought. presumably description generic the in growing not Bentham's seen Genera Plantarum 1 generic name). Also because Bentham had he described 2. Mastersia bakeri M. bakeri (Koord.) Blumea Minah. 5 Backer (Koord.) Backer in 194; (1942) Heyne, Backer & 17702 an with area a yearly (L); s y Nutt. PI. Ned. Bakh. Fl. t n f., e Ind. 2nd Java 1 ed., (1964) 16; Koorders : the of the use Baker material, only same thought superfluous epithet cleistocarpa. (1922) pi. 2 y p of M. assamica, description (proved by 1a-e. Fig. - Cel. (1898) 439, 630; Suppl. type: Koorders in annotated his not when he created the species a new moist soil on Altitude 80—1250 m. not rare. Baker has Note. the in trees; climbing Occurrence 2 Mucuna - 3 Cel. Suppl. 17705 Holthuis (1927) 828; 631. & bakeri (1922) 9. - (L), Celebes, Minahassa, Lam, Koord., LectoMenado. See note 1. M. borneensis (1921) 2211 M. Harms in Kema. Harms 15( —18) 3.5-6 nerves 6—14 lower surface, Southeast 1.5-4 by on each side stalked long; 2 c. 1 by 20 broadly up 12—18 J. Str. Br. Elm. Born. 369. As. Roy. 109. (1929) Type: - Sarasin No. Soc., Spec. Type: - Winkler 250 (B lost), Celebes, by c. long. Wing 6 blade slightly mm curved Disk upwards by c. mm. 1.5 a 3—5 mm long dorsal lobe 7—14 by 6—9(—11) sculpturing mm long; upper after mm sometimes 0.7—2 3—7 acumen upper and on mm 0.8 at a long; Pseudoracemes 6- base, 1.5—5 by 1—3 mm; c. ventral lobe 7—14 5 mm. Standard claw absent mm; indistinct to mm Pedicel 1.5—5 mm. cup, by 8— mm. especially to claw mm mm. by c. elliptic occasionally 1.5—2.5 mm distinct. Keel blade transition between claw and blade margin. lobes 0.5—2 by Brachyblasts 0.5—3(—6) 8—14(—16) by 2.5—3.5(—4) the 2.5—6 present. by dorsally touching developed; at pubescent 1.2 the flowers mm; claw 2.5—3.5 long. 4.5 with 8—14(—17) pocket present 12—16 long, mm; to c. Rachis, infrajugal part 3.5—14 cm; by glands occasionally Bracteoles 4 revolute. long. Stipellae midrib; usually Bracts c. to cm 4.5—15.5 cuspidate, by convex 1.5—3.8 long. Calyx ovate; blade mm lateral ments mm mm lower auricle long; ual; to lateral lobes 6—1 1 (1911) mm, scar of the mm. pubescent. to 9 and unstalked Flowers up to PI. Borneo, Hayoep. long. Leaflets mm bracts ovate, bracts mm; (1911) 369; Merr., (1928) 524; Fedde, Rep. long, sparsely 4 3 long; ultrajugal part cm Petiolules 6—8 long; in 9 Rep. J. See note 2. Stipules cm Mus. (B lost, L, SING), sarasinorum 30 Fedde, Sarawak 310; grad- Staminal tube and free of filapart long. Ovary slight c. 10 mm long; style downward bend. Pod 5—13 c. 6 by BLUMEA 86 2—3 2.5 with cm, ventral wing mm; radicle Field 7.5—18.5 green when from varying green young via 1.5 broad, mm 5.5 c. by 5—12.5 Inner cm. on and yellow and the inside near reddish pink dark to pale bark lower side. on Calyx mature. red, crimson its base. Smell faint. Fruits black. Seeds dark, yellow turning In Ecology. and primary to being present to forest secondary hillsides; type recorded: yellow, clayish plants Celebes, Moluccas. Occasionally (see uses). spots; from flat grounds m — long; embryo crimson and reddish brown when young via green-yellow girth Distribution. North Borneo, Central and North cultivated in Java 900 1 wing mm brown. greyish some 5 c. upper side, light green dark to green when long, m on when mature; standard with green spot green when young, dorsal edges, long. glossy to dark from Corolla mm Climber, notes. green. Leaves varying 2 1984 1, broad. Seeds 5-20, funicle mm c. No. 30, both wings along longitudinal 2—3 VOL. - sand on on to dry places. hill of volcanic tuff. Occurrence in groups to being in open grounds, especially waste (like riverbanks) wet on One soil from varying found from sealevel up common; to altitude. Vernacular Moluccas: N. Celebes names. abele (Morotai I.), rarau (Sulawesi utara): lambuow, tatamulak, tontagis. Halmahera: (N. Gal.), wolewon Halmahera: (S. Weda). Uses. which used According prevents as as it nodulates as coverplant a establishment of Pollen. I.K. & Ferguson J.J. Skvarla Papilionoideae (Leguminosae). systematics 2, 1981, 886, 'less specialised'; they are lumina. Endexine is much with the grains Notes. Koorders, of Pueraria l.The 1922) manuscript. oldest, was Koorders ' the too 11: 888, pi. narrower Koorders, merely Then the Backer first (the valid first make to as it a is sons. Firstly, has the been plant can because of its climb- of the Advances subfamily in legume that the grains of M. bakeri reticulate with layer be recom- f., 1964). morphology of the reprint this granules much broader in are in the comparison is bakeri. species the new even combination, but in (Kds.) Back.).' smaUer. consequently not of a very 16 authors accepted (Art. Heyne (1922) a plate most not was valid combination is in of the first edition Under Although the combination new (see Backer combination within Mastersia in bakeri printed synonym, and pubUcation the aid of name new (= Mastersia 34 by ICBN). (1927) Heyne's by book Backer). 2. The type of M. sarasinorum Harms rial. The the obvious that introduction of the acknowledges for legitimate epithet Mucuna bakeri Kds. cited The phaseoloides. (1922), however, published (1922), Bakh. good coverplant, a much Utter. It is plantations pollen and the foot combination within Mastersia is Koorders (The & subprolate, margocolporate, the to tea (Backer G, H) report way: refer in produces as grasses. R.M.Polhill & P.H. Raven, In: pecuUar new alang-alang and easily plantations, except in habit. It is sometimes used in Java ing in N. Celebes Heyne (1927) appreciated to dominating fertilizer too, a mended the placed was not studied, because of loss of the into the synonymy of M. bakeri because of differences Harms (1911) has described among M. mate- two rea- sarasinorum and P. C. the other most important calyx with Welzen differences shorter & S. den The Hengst: cup that are and with relatively The plants tinct doubt that only of the Moluccas show often (but leaving sculpturing bends a islands. The little downwards before plants A 2057: Brooke 2 1824: U. 2390: 1 de - - 2 2; SF 6705: 2362: 2. 2 Haan 1 - van - 2 Tessier - Kaudern - 3500: 2; 2 2 - 3580: 2 2 1 - Prain 70610: 204: 2; 1 - 21794: 3247: 272: 2 71053: de show blades with a dis- in the other which sometimes style, a is present. species 1 - - - 2; Vogel STUDIED = - - M. 1905: Beguin Clarke 2 8916: - Monod Idjan 79130: 3816: 2; - & 2 - 2; 5179: 79789: 5639: 2 - = M. bakeri 2108: - 3439: 2; 2 222: 17702: 2; - 2 Clemens 2; 71:25414: 79833: 2 2 1; - 2; Winkler 216: 2 21186: 1; 2; 2211: - 1 - 1; - Kostermans 10787: 81018: 2 694: 48913: Ooststroom Ras 2; - 1 21294: 2; 522: Joseph 17705: van 16347: Elmer - - Bor 10070: Griffith 515: Mochtar 17698: 2; 1 Curran de Froideville Purseglove 2; 40752: 27321: 2 2 assamica; Geesink Koorders - 306: 2 204: 2; 2 246: Hulstijn Lewis 1 Burut 3096: Eyma - 1807: 21605: - different from only slightly developed of Celebes included. Balgooy 2 hexandra); 4958: 57052: 2 2 BS 425: - Dioclea 2; Lam - Panigrahi 26681: 3218: 4225: Kanjilal 21300: 2 with (mixed Endert 2; 10148: variable a later curving upwards. not been collections have Secondly, slightly very exclusively) wing not COLLECTIONS Unnumbered only minimal. The are smaller bracteoles and ventral lobe. slightly one the upper auricle, which is near of other specimens no bakeri) M. has longer collected material from Celebes and the Moluccas is that of Borneo, = M. sarasinorum a 87 genus Mastersia assamica and M. borneensis species (M. two a van 12698: 1 - 83919: 2 - SAN 2 - Yoshida