A nomenclator of Pacific oceanic island Phyllanthus (Phyllanthaceae), including Glochidion.

Recent molecular phylogenetic studies and reevaluation of morphological characters have led to the inclusion of Glochidion within a broader delimitation of Phyllanthus. It is necessary for preparation of the Vascular Flora of the Marquesas Islands to make new combinations for the Marquesan species. We also provide the relevant combinations and listing of all of the currently accepted species of Phyllanthus on Pacific oceanic islands for a total of 69 native species in oceanic Pacific islands. Glochidion tooviianum J. Florenceis here placed into synonymy of Phyllanthus marchionicus (F. Br.) W. L. Wagner & Lorence based on new assessment of recently collected specimens from Nuku Hiva. Glochidion excorticans Fosberg var. calvum Fosberg is placed into synonomy of Phyllanthus ponapense (Hosokawa) W. L. Wagner & Lorenceand Glochidion puberulum Hosokawa and Glochidion excorticans Fosberg are placed in synonymy of Phyllanthus senyavinianus (Glassman)W. L. Wagner & Lorence based on new study of all Micronesian specimens available to us. No infraspecific taxa are recognized within Phyllanthus pacificus of the Marquesas Islands. Species already with valid names in Phyllanthus are also listed for completeness and convenience. Brief distributional comments are given for each species. We propose new names for species for which a new combination is not possible: Phyllanthus florencei W. L. Wagner & Lorence, nom. nov., Phyllanthus mariannensis W.L. Wagner & Lorence, nom. nov., Phyllanthus otobedii W. L. Wagner & Lorence, Phyllanthus raiateaensis W. L. Wagner & Lorence, Phyllanthus st-johnii W. L. Wagner & Lorence, nom. nov., and Phyllanthus vitilevuensis W.L. Wagner & Lorence, nom. nov. We provide information for four additional naturalized species within the region (Phyllanthus amarus, Phyllanthus debilis, Phyllanthus tenellus, and Phyllanthus urinaria). The name Glochidion ramiflorum widely applied to Pacific island populations is here considered to be a species further west in the Pacific with all of the oceanic species here referred to several regional species.

Introduction

Recent molecular phylogenetic studies have greatly advanced the understanding of relationships in the family Phyllanthaceae (a segregate from Euphorbiaceae s. l.) based on chloroplast and nuclear DNA sequence data (Wurdack et al. 2004; Samuel et al. 2005; Kathriarachchi et al. 2005, 2006). Among the tribes in Phyllanthaceae (Hoffmann et al. 2006), tribe Phyllantheae is the largest natural group and accounts for more than half of the 2000 species in the family (Kathriarachchi et al. 2006; Hoffmann et al. 2006). One of the most taxonomically difficult groups in the family is L.and related genera, species of which have small unisexual flowers and an often confusingly similar habit in unrelated groups. Historically generic circumscriptions in Phyllantheae have undergone substantial fluctuation, and the definition of natural groups is still unclear in many parts of the tribe (Hoffmann et al., 2006). The recent molecular studies of relationships within the family, with special emphasis on the large genus , confirm paraphyly of in its traditional circumscription with J. R. Forst. & G. Forst., Glochidion J. R. Forst. & G. Forst., Reverchonia A. Gray, and Blumeembedded within . These results led the research groups working on Phyllanthaceae (Hoffmann et al. 2006; Kathriarachchi et al. 2006) to conclude that the embedded genera should be submerged into a broadened rather than further generic segregation, which would create a series of highly technical genera distinguishable only by specialists. Distinguishing morphological characters among these five taxa are not clear-cut or comparable, and thus recognition of equivalent clades at generic level would exacerbate the problem of understanding the evolution of this large and widespread lineage (Hoffmann et al. 2006). The enlarged comprises nearly 1300 species with the inclusion of , , , Hemsl., and . It is not surprising that the vast morphological diversity of prior to adding the embedded taxa would readily accommodate them (Hoffmann et al. 2006). Unfortunately, the broadening of necessitates a considerable number of new combinations, but nevertheless this seems to be the best approach over the long term in the interest of developing a classification that facilitates understanding of the evolution and relationships in the overall group.

Our work has focused on the oceanic Pacific and specifically we are currently completing investigation of the flora of the Marquesas Islands as part of a collaboration between National Tropical Botanical Garden (NTBG), Smithsonian Institution (SI), and the Délégation à la Recherche, Papeete, Tahiti (French Polynesia). We do not believe it is wise to make only the necessary combinations for just the Marquesan species previously placed in so we here provide a synopsis of all of the Pacific oceanic island species (Fiji and Caroline Islands eastward across the Pacific). We also include all of the species currently recognized within for completeness. We have not made an exhaustive study of the taxonomy of these species, but accept for the most part previous taxonomic conclusions. The Pacific group of species is in serious need of comprehensive analysis as previous work has focused on localized areas with few excePageBreakptions. Smith (1981) and Florence (1997) have made good regional taxonomic studies, but both point out problems that need a broader geographical perspective to solve. The Micronesian species are in particular need of comprehensive study and have received only partial treatments, either of part of the region (Hosokawa 1935) or more superficial descriptive work (Fosberg and Oliver 1991) without consideration of all species previously described. We have made some changes to the taxonomy of these species, but an in depth study is required to gain a more solid understanding of the diversity within Micronesia. Webster (1986) also made a partial study in the region, primarily of southwestern Pacific species, and Croizat (1943) contributed a useful analysis of several species. We have made extensive use of the Euphorbiaceae world checklist (Govaerts et al. 2000) in compiling the list presented here.

Systematics

1. Müll. Arg., Flora 48: 390. 1865. TYPE. FIJI ISLANDS: Vanua Levu: Mbua Bay, 1840, U.S. Expl. Exped. s.n. (holotype: probably G; Isotype: US!).

(Müll. Arg.) Kuntze, Revis. Gen. Pl. 2: 598. 1891. Müll. Arg.) Croizat, Sargentia 1: 46. 1942.

Distribution. Endemic to Fiji and known from Vanua Levu and eastern Viti Levu at elevations of 100–400 m in dense or open forest, edges, and thickets (Smith 1981).

2. G. Webster, Pacific Sci. 40: 100. 1986 [1988]. TYPE. TONGA: Eua, E. Soakai 341 (Holotype: K).

Distribution. Endemic to the island of Eua, Tonga (Webster 1986) where it is only known from forest margins and exposed rocks, 300m, on the Liku Plateau.

3. (Gibbs) W. L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112692-1

Basionym: Gibbs, J. Linn. Soc. Bot. 39: 168. 1909. TYPE. FIJI ISLANDS: Viti Levu: Nandarivatu, Sep 1907, J. G. Gibbs 730 (holotype: BM).

Distribution. Endemic to Fiji and known only from Viti Levu and Ovalau at elevations from 100 to 1075 m, in dense or dry forest, thickets or ridge forest (Smith 1981).

4. Nadeaud, Énum. Pl. Tahiti 73. 1873. TYPE. SOCIETY ISLANDS: Tahiti: 1000 m, Nov 1857, J. Nadeaud 459 (holotype: P; isotypes: G [2], P[2]).

Distribution. Endemic to the Society Islands and known only from Tahiti at about 1000 m elevation on a ridge crest. Not collected since 1857 and presumed extinct (Florence 1997).

5. (A.C. Sm.) W.L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112693-1

Basionym: A.C. Sm., Contr. U.S. Natl. Herb. 37: 74. 1967. TYPE. FIJI ISLANDS: Viti Levu: Namosi, northern Korombasambasanga Range, drainage of Wainavindrau Creek, 450 to 600 m, 28 Sep 1953, A.C. Smith 8747 (holotype: US-02191397!; isotypes: GH, BISH!, L, NY!, S).

Distribution. Endemic to Fiji and known only from Namosi Prov., Viti Levu from 250–800 m in dense forest (Smith 1981).

6. (A.C. Sm.) W.L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112694-1

Basionym: A.C. Sm., Fl. Vitiensis Nova 2: 481,491. 1981. TYPE. FIJI ISLANDS: Viti Levu: Serua, hills between Waininggere and Waisese Creeks, between Ngaloa and Wainiyambia, 50 to 100 m, 10 Dec 1953, A.C. Smith 9550 (holotype: BISH-508142!; isotype: US!).

Distribution. Endemic to Fiji and know only from coastal and slightly inland areas of southern Viti Levu from 50–100 m in dry or dense forest (Smith 1981).

7. (Gillespie) W.L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112695-1

Basionym: Gillespie, Bernice P. Bishop Mus. Bull. 91: 15. 1932. TYPE. FIJI ISLANDS: Viti Levu: Rewa, SE slopes of Mt. Korombamba, 7 Aug 1927, J. W. Gillespie 2169 (holotype: BISH-508144!; isotypes: BISH [2]!).

Distribution. Endemic to Fiji from southern and eastern Vitu Levu, from 100 to 430 m in dense or open forest (Smith 1981).

8. (J. Florence) W.L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112696-1

Basionym: J. Florence, Fl. Polynésie Française 1: 68. 1997. TYPE. SOCIETY ISLANDS: Raiatea: Opoa, Mont Oropiro, épaulement nord. 200 m, 151°24’ W, 16°51’ S, 2 Jun 1990, J. Florence 10373 (holotype: P; isotypes: BISH!, CHR, DAV, K, L, P, PAP, PTBG!, US!).PageBreak

Distribution. Endemic to the Society Islands and know only from Raiatea at apparently only low elevations from 200 to 250 m, collected in riparian forest with L. and in mesic ridge forest with (J. R. Forst. & G. Forst.) A. Gray and (L.) Merr. (Florence 1997) The area has been converted to pine plantation (D. Hembry, pers. comm. 2011).

9. (A.C. Sm.) W.L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112697-1

Basionym: A.C. Sm., Fl. Vitiensis Nova 2: 482, 491. 1981. TYPE. FIJI ISLANDS: Viti Levu: Namosi, Mt., Nambui, third peak of Korombasambasanga Range, 12 Nov 1965, DA 14548 pro parte (coll. D. Koroiveibau & I. Qoro) (holotype: BISH-508147!; isotype: SUVA).

Distribution. Endemic to Fiji and know only from inland areas of Viti Levu and Vanua Levu, from 300 to 960 m in dense forest, ridge forest and scrubby forest (Smith 1981).

10. (Croizat) W.L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112698-1

Basionym: Croizat, Sargentia 1: 46. 1942. TYPE. FIJI ISLANDS: Fulaga: limestone cliff of lagoon, 0 to 80 m, 26 Feb 1934, A.C. Smith 1217 (holotype: GH; isotypes: BISH!, K, S, US!).

Distribution. Endemic to Fiji and know only from the two islands of southern Lau (Fulaga and Kabara) near sea level on limestone and lagoon cliffs (Smith 1981).

11. (Croizat) W. L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112699-1

Basionym: Croizat, Occas. Pap. Bernice P. Bishop Mus. 17(16): 213. 1943. TYPE. SAMOAN ISLANDS: Savai`i: above Matavanu, 1300 m, 24 Jul 1931, E. Christophersen & E. P. Hume 2134 (holotype: A; isotype: BISH).

Distribution. Endemic to montane Savai`i and known from cloud forest at 1000–1550 m (Whistler 1978; Christophersen 1935).

12. (Fosberg) W. L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112700-1

Basionym: Fosberg, Willdenowia 20: 263. 1991. TYPE. CAROLINE ISLANDS: Pohnpei: 1913, C. L. Ledermann 13599a (holotype: B-bc100249519!)

PageBreakDistribution. Endemic to Pohnpei where it occurs from ca. 12 to 770 m elevation, most commonly in lowland wet forest and agroforest, but occasionally in summit cloud forest.

Note. This species is distinctive in having oblong-ovate to narrowly oblong-elliptic leaves and comparatively small flowers in umbel-like fascicles often borne on short, sometimes branched stalks or peduncles to 5 mm long, a densely puberulent pistil with a puberulent columnar style exserted for 1–1.5 mm beyond the calyx lobes, and relatively small, densely puberulent fruits. Pohnpei collections of this species have been identified as or less commonly .

13. (J. Florence) W. L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112701-1

Basionym: J. Florence, Novon 7:29. 1997. TYPE. PITCAIRN ISLANDS: Pitcairn: Sommet Crete Sud-Est, 25°4’ S, 130°7’ W, 300 m, 19 Apr 1991, J. Florence 10740 (holotype: K; isotypes: BISH, BM, DAV, E, L, MO, P, PAP, TER, US!).

Distribution. Endemic to Pitcairn where it is known from fewer than 10 collections.

14. (Müll. Arg.) Müll. Arg., Flora 48: 374. 1865.

Basionym: Müll. Arg., Linnaea 32: 62. 1863. var. ellipticus (Müll. Arg.), Prodromus Systematis Naturalis Regni Vegetabilis 15(2): 290. 1866, nom. illeg. (Müll. Arg.) Kuntze, Revis. Gen. Pl. 2: 599. 1891. TYPE. FIJI ISLANDS: s.l., Nov 1855, W. H. Harvey s.n. (holotype: P; isotypes: BM, K).

J.R. Forst. & G. Forst. var. lanceolatum Müll. Arg. Linnaea 32: 63. 1863. (J.R. Forst. & G. Forst.) Müll. Arg. var. lanceolatus (Müll. Arg.) Müll. Arg., Flora 48: 374. 1865, nom. illeg. TYPE. FIJI ISLANDS: Ovalau: Port Kinnaird, June 1860 and Somosomo, Taveuni, May 1860, B.C. Seemann 415 (lectotype: presumably G, designated by Smith (1981, p. 476); isolectotypes: BM, K).\\

Distribution. Widespread in Fiji, Tonga, and possibly Raratonga (Smith 1981), and also from Niue (Sykes 1970) from 0 to 1000 m elevation in dense or open forest, edges and forest-grassland transition, and on open slopes. These collections were previously referred to , butwere considered by Smith (1981) to be a separate species. He considered to be a species from New Guinea to New Hebrides.

15. (Seem. ex Müll. Arg.) Müll. Arg., Flora 48: 376. 1865.

Basionym: Seem. ex Müll. Arg., Linnaea 32: 64. 1863. (Seem. ex Müll. Arg.) Kuntze, Revis. Gen. Pl. 2: 599. 1891. TYPE. FIJI July 1860 and Ovalau: Port Kinnaird, June 1860 [the K isotype bears 2 field labels], B.C. Seemann 416 (holotype: presumably G; isotypes: BM, K).

Distribution. Endemic to Fiji and know from Viti Levu, Ovalau, and Vanua Levu at 50–900 m, in dry forest, ridge forest, and in pastures and along roadsides (Smith 1981).

16. Müll. Arg., Flora 48: 377. 1865.

Basionym: (Müll. Arg.) Pax, Bot. Jahrb. Syst. 25: 645. 1898. (Müll. Arg.) Kuntze, Revis. Gen. Pl. 2: 599. 1891. TYPE. SAMOAN ISLANDS: s.l., U.S. Expl. Exped. s.n. (holotype: G-DC).

Distribution. Endemic to the Samoan Islands (Savai`i, `Upolu), and Tutuila at up to 400–450 m in ridge forest (Whistler 1980).

17. Hook. & Arn., Bot. Beechey Voy.: 95. 1832.

Basionym: (Hook. & Arn.) Kuntze, Revis. Gen. Pl. 2: 599. 1891. TYPE. HAWAIIAN ISLANDS: O`ahu: 1827–1827, G.T. Lay & A. Collie s.n. (probable holotype: K; probable isotype: E).

Distribution. is endemic to the Hawaiian islands where it is occasional to locally common in mesic forest, often on steep slopes or ridge tops, sometimes in dry shrubland at 60–950 m on the islands of Kaua`i, O`ahu, Moloka`i, Lana`i, West Maui, and rare on East Maui. A number of additional names have been applied to populations of , but they were placed into synonymy by Wagner et al. (1990, 1999) and are not repeated here.

18. (J. W. Moore) W. L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112702-1

Basionym: J. W. Moore, Bernice P. Bishop Mus. Bull. 102: 30. 1933. TYPE. SOCIETY ISLANDS: Raiatea: Mount Temehani, 470 m, 1 Jan 1927, J.W. Moore 476A (holotype: BISH-508150!; isotype: P [2]).

J. W. Moore, Bernice P. Bishop Mus. Bull. 102: 30. 1933. TYPE: SOCIETY ISLANDS: Raiatea: Mount Temehani, 470 m, 1 Jan 1927, J.W. Moore 476B (Holotype: BISH-508230!).

Distribution. Endemic to the Society Islands and known only from Raiatea at 580–750 m where it occurs in marshy shrubland with and species of Cyperaceae. Also collected at ca. 930 m in mesic ridge shrubland with and (Florence 1997).

PageBreak19. (A. C. Sm.) W. L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112703-1

Basionym: A.C. Sm., J. Arnold Arbor. 33: 373. 1952. TYPE. FIJI ISLANDS: Viti Levu: Mba, upper slopes of Mt. Koromba (Pickering Peak), 3 Jun 1947, A. C. Smith 4659 (holotype: A; isotypes: BISH!, K, S, US!).

Distribution. Endemic to Fiji and known only from the type collection.

20. W. L. Wagner & Lorence, nom. nov.

urn:lsid:ipni.org:names:77112704-1

Replaced name: J. Florence, Fl. Polynésie Française 1: 90. 1997. TYPE. SOCIETY ISLANDS: Tahaa: Patio, Mt. Purauti, crête sud-est, 151°30’ W, 16°37’ S, 225 m, 18 Jun 1990, J. Florence 10,627(holotype: P; isotypes: BISH!, CHR, DAV, K, L, NY!, P [2], PAP, PTBG!, US!).

Distribution. Known from the Society Islands (Huahine, Mauapiti, Raiatea, and Tahaa) and Austral Islands (Rimatara) at 0–225 m elevation where it is locally common to abundant in coastal vegetation with and on coral sand, in lowland mesic forest with and , in mesic ridge forest with and (Burm. f.) Underw., and in secondary forest (Florence 1997).

21. (Croizat) W.L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112705-1

Basionym: Croizat, Sargentia 1: 46. 1942. TYPE. FIJI ISLANDS: Viti Levu: Namosi, near summit of Mt. Naitarandamu, 28 Sep 1927, J.W. Gillespie 3161 (holotype: GH; isotypes: BISH).

Distribution. Endemic to Fiji and known only from mountainous areas of Viti Levu from 750–1155 m in dense or ridge forest (Smith 1981).

22. (J. Florence) W. L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112706-1

Basionym: J. Florence, Bull. Mus. Natl. Hist. Nat., B, Adansonia 18: 250. 1996. TYPE. SOCIETY ISLANDS: Tahaa: Tapuamu, crête entre les Monts Tete et Ohiri. 530 m, 151°31’ W, 16°37’ S, 5 Nov 1992, J. Florence & R. Tahuaitu 11816 (holotype: P; isotype: BISH!, DAV, K, L, PAP, US!).

Distribution. Endemic to the Society Islands (Raiatea and Tahaa) where it occurs at 435–730 m elevation in marshy shrubland with and Cyperaceae and in wet summit forest with and (Florence 1997).PageBreak

23. Müll. Arg., Flora 48(24): 380. 1863.

(Müll. Arg.) Kuntze, Revis. Gen. Pl. 2: 599 .1891. (Müll. Arg.) J. Florence, Bull. Mus. Natl. Hist., B, Adansonia 18: 250. 1996. TYPE. SOCIETY ISLANDS: Tahiti: s. l., Sep 1839 or Jan1841, U. S. Expl. Exped. s.n. (Holotype: G-DC).

Distribution. Endemic to the Society Islands and known only from Tahiti at 60–1040 m. It occurs in lowland riparian forest with and and extends up to mesic ridge and summit forest dominated by (Florence 1997).

24. Müll. Arg., in DC., Prodr. 15(2):321. 1866.

(Müll. Arg.) Kuntze, Revis. Gen. Pl. 2: 599. 1891. (Müll. Arg.) Pax & K.Hoffm. in H.G.A. Engler, Nat. Pflanzenfam. ed. 2, 19c: 58. 1931. TYPE. FIJI ISLANDS: s. l.,1840, U.S. Expl. Exped. s.n. (Holotype: Probably G).

Distribution. Endemic to Fiji and known only from Vanua Levu and Lau Group, Fulaga from 0 to 870 m (Smith 1981).

25. (J. Florence) W. L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112707-1

Basionym: J. Florence, Fl. Polynésie Française 1: 74. 1997. TYPE. MARQUESAS ISLANDS: Hiva Oa: Atuona, piste de Hanamenu, NW du Mt. Temetiu, 139°5’ W, 9°48’ S, 1100 m, 30 Jul 1988, J. Florence & S. Perlman 9673 (holotype: P; isotypes: BISH!, DAV, K, L, P, PAP, PTBG!, US!). Fig. 1.

Figure 1.

(J. Florence) W. L. Wagner & Lorence. A branch B abaxial leaf surface C leaf axil showing stipules D female flowers E female flower close-up F–G calyx lobes H longitudinal view of female flower I capsule. A–I drawn from: Marquesas Islands. Tahuata: Haaoiputeomo, summit ridge, 823-951 m, Wood et al. 6522(BISH, DAV, K, MO, P, PAP, PTBG, US).

Distribution. Endemic to the Marquesas Islands of Hiva Oa and Tahuata, from about 700 to 1200 m, collected in wet shrubland and forest with , , and the tree ferns and (Florence 1997).

26. (Fosberg) W. L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112708-1

Basionym: Fosberg, Willdenowia 20: 261. 1991. TYPE: CAROLINE ISLANDS: Pohnpei: Awak, 25.8.1980, F.R. Fosberg 60467 (holotype: US [not located]: isotypes: BISH, L).

Distribution. To date know only from the type collection from Pohnpei; the holotype could not be located at US.

Note. This entity should be carefully evaluated in the context of an overall review of in Micronesia. It may be conspecific with , in which PageBreakPageBreakcase we would adopt the latter name because the description applies most closely to this species and the holotype is available at B.

27. (J. Florence) W. L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112709-1

Basionym: J. Florence, Fl. Polynésie Française 1: 75. 1997. TYPE. SOCIETY ISLANDS: Huahine: Maeva, motu Oavarei, secteur Haaparu, 151°W, 16°41’ S, 2 m, 1 Nov 1992, J. Florence & R. Tahuaitu 11745 (holotype: P ; isotypes: BISH, DAV, K, L, NY, P, PAP, PTBG !, US !).

Distribution. Endemic to the Society Islands and known only from Huahine on the islet Motu de Maeva at 1–4 m elevation, restricted to coral sand substrate in coastal vegetation with , , and (Florence 1997).

28. (A.C. Sm.) W.L. Wagner & Lorence, comb. nov.

Basionym: A.C. Sm., Fl. Vitiensis Nova 2: 486, 493. 1981. TYPE. FIJI ISLANDS: Vanua Levu: divide between Wainunu and Ndreketi Rivers, between Nanduna (old village site) and Mt. Ndelanathau, 17 May 1934, A.C. Smith 1851 (holotype: BISH-142932; isotypes: many indicated, but not specific as to where deposited).

Distribution. Endemic to Fiji and known only from the type.

29. Müll. Arg., Linnaea 32: 21. 1863. TYPE. s. l., D.E.S.A. Jardin s.n. (holotype: G-DC-FP3347; isotypes: P [2]). Type presumed to be from Nuku Hiva in the Marquesas Islands.

urn:lsid:ipni.org:names:77112710-1

Note. Precise locality uncertain, known only from a single collection possibly made in the Marquesas Islands (Nuku Hiva) by Jardin in the 19th century (Florence 1997).

30. (Hosokawa) W. L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112711-1

Basionym: Hosokawa, Trans. Nat. Hist. Soc. Taiwan 25: 22. 1935. TYPE. CAROLINE ISLANDS: Palau: Jul–Aug 1929, R. Kanehira 241 (holotype: TAI).

Distribution. Caroline Islands: Palau (Peleliu, Koror including the Rock Islands of Mecherchar, Ngeruktabel, Ulebsechel and Urukthapel, and also known from Babeldaob [Fosberg et al. 1979; Wagner et al. unpubl.]), Yap (Yap Island), and Chuuk (Moen Island, also Tol, Udot, Uman, Dublon, Fano, Fanurmot [Fosberg et al. 1979; Wagner et al. unpubl.]). On Palau it is restricted to limestone substrate from near sea level to about 200 m elevation in coastal forest with speices of , PageBreak, , , and , and in lowland evergreen forest with and and agroforest. On Chuuk it occurs near sea level (3 m) in coastal forest interspersed with mangroves and on slopes of unknown elevation in agroforest and secondary vegetation. On Yap it occurs from near sea level at the edge of mangrove vegetation and on slopes up to 40 m with secondary vegetation.

Note. This glabrous species is characterized by female flowers with a small, depressed-globose pistil 1–1.5 mm long with a very short 10–11-fid stylar column 0.5 mm long. Certain collections from Yap have been identified as cf. ramiflorum, and certain collections from Palau have been identified as .

31. L. Riley, Bull. Misc. Inform. Kew [2]:55. 1926.

(L. Riley) F. Br., Bernice P. Bishop Mus. Bull. 130: 141. 1935. TYPE. AUSTRAL ISLANDS: Rapa: L.A.M. Riley 776 (holotype: K; isotype: BM).

Distribution. Endemic to the Austral Islands (Rapa) where it occurs from 140 to 575 m, in mesic forest on slopes and in valleys and ravines with species of and (Florence 1997).

32. (Hosokawa) W. L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112712-1

Basionym: Hosokawa, Trans. Nat. Hist. Soc. Taiwan 25: 21. 1935. TYPE. CAROLINE ISLANDS: Palau: Babeldaob, valley near Mt. Agade, “Arukoron-sogan”, 20 Sep 1933, T. Hosokawa 7053 (holotype: TAI-118940; isotypes: BISH, GH, TAI). Holotype presumed to be the TAI sheet with the typewritten label as is typical of Hosokawa collections.

Distribution. Endemic to Palau (Babeldaob, Anguar, Peliliu, and Malakal Islands), where it occurs at 3–150 m, in lowland evergreen moist and wet forest on limestone and limestone-derived soils.

Note. This glabrous species is characterized by female flowers with relatively large calyx lobes enclosing the short, depressed-ovoid pistil 1.5 mm long with a very short style column and flat 5-6-sulcate or -lobed stigmatic region. In male flowers the staminal column is composed of 5 connate stamens (versus 3-4 in other Micronesian species).

33. (Baill. ex Müll. Arg.) Müll. Arg., Flora 48: 377. 1865.

Basionym: Baill. ex Müll. Arg.,Linnaea 32: 65. 1863. (Baill. ex Müll. Arg.) Kuntze, Revis. Gen. Pl. 2: 600. 1891. TYPE. SOCIETY ISLANDS: Tahiti: s. l.,J. Lepine 210 (lectotype: G-DC, designated by Florence, Fl. Polynésie Française 1: 79. 1997; isolectotypes: P [2]).

PageBreakDistribution. Endemic to the Society Islands of Moorea and Tahiti where it occurs at 30–1000 m, in valleys in wet forest with , , and and also on slopes and summits, sometimes in disturbed or secondary forest with , , and (Florence 1997).

34. (F. Br.) W. L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112713-1

Basionym: F. Br., Bernice P. Bishop Mus. 130: 142. 1935. TYPE. MARQUESAS ISLANDS: Ua Huka: 9 Nov 1922, E. H. Quayle 1689 (Lectotype: BISH-508228! & 508229!, designated by St. John, Phytologia 33: 420. 1976). Fig. 2.

Figure 2.

(F. Br.) W. L. Wagner & Lorence. Branch with dehisced fruit showing red arillate seeds, with trunk in background. Field image by K. R. Wood: Marquesas Islands. Ua Huka, Haahue, northwestern coastal valley,Wood 10765 (PTBG, US).

Glochidion tooviianum J. Florence, Bull. Mus. Natl. Hist. Nat., B, Adansonia 18: 260. 1996, syn. nov. TYPE. MARQUESAS ISLANDS: Nuku Hiva: Toovii, 800 m, 140°9’ W, 8°51’ S, 3 Mar 1986, J. Florence 7445 (holotype: P; isotypes: BISH!, P, PAP, US).

Distribution. Endemic to the Marquesas Islands (Nuku Hiva, Ua Huka, Ua Pou, Hiva Oa, Tahuata, and Fatu Hiva) from 50 to 1130 m, where it is widespread in moist valleys with , disturbed mesic ridge forest with , ,and , and secondary vegetation with , , ,and or in primary wet forest with , , , and tree ferns (Florence 1997).

35. W.L. Wagner & Lorence, nom. nov.

urn:lsid:ipni.org:names:77112714-1

Replaced name: Müll. Arg., Linnaea 32: 65. 1863. Muell.-Arg. var marianus (Müll. Arg.) Müll. Arg., in DC. Prodr. 15(2): 300. 1866. TYPE. MARIANA ISLANDS: Guam: C. Gaudichaud-Beaupré 139(holotype: G-DC).

Distribution. Endemic to the Mariana Islands (Guam) where it occurs on limestone and basaltic soils in old fields and grasslands and disturbed native and secondary vegetation at ca. 60–150 m elevation.

Note. The ovate leaves with short acuminate to rounded apices and glabrous columnar style 1.5–2 mm long exserted beyond the calyx lobes are characteristic of this species. Collections from Caroline Islands (Pohnpei) previously identified as this species are here considered to represent .

36. Müll. Arg., Linnaea 32:17. 1863.

(Müll. Arg.) Kuntze, Revis. Gen. Pl. 2: 600. 1891. TYPE. MARIANA ISLANDS: Guam: s.l., 17 March to 3 April 1819, C. Gaudichaud-Beaupré s. n. (holotype: G-DC).PageBreak

Distribution. Endemic to the Mariana Islands (Guam, Aguijan, Agrihan, Alamagan, Anathan, Asuncion, Guguan, Maug, Pagan, Rota, Saipan, Sarigan, Tinian) and the Caroline Islands (only on Ulithi Atoll). On Guam it is common on limestone cliffs and terraces.

PageBreak37. (Airy Shaw) W.L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112715-1

Basionym: Airy Shaw., Kew Bull. 25: 487. 1971. TYPE. FUJI ISLANDS: Viti Levu: Nausori Highlands, Nandronga and Navosa Province, 2 May 1962, R. & E.F. Melville & J.W. Parham 7048 (holotype: K; isotypes: BISH, SUVA).

Distribution. Endemic to Fiji and known only from the vicinity of the type locality at 600–670 m in dense or mixed forest (Smith 1981).

38. (A.C. Sm.) W.L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112716-1

Basionym: A.C. Sm., Fl. Vitiensis Nova 2: 484, 493. 1981. TYPE. FIJI ISLANDS: Vanua Levu: Thakaundrove Prov., SW slope of Mt. Batini, 28 Nov 1933, A.C. Smith 606 (holotype: BISH-142931; isotypes: many indicated, but not specific as to where deposited).

Distribution. Endemic to Fiji and know only from Mt. Batini and Mt. Seatura on Vanua Levu from 300 to 800 m in dense or crest forest (Smith 1981).

39. (J. Florence) W. L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112717-1

Basionym: J. Florence, Bull. Mus. Natl. Hist. Nat., B, Adansonia 18: 253. 1996. TYPE. SOCIETY ISLANDS: Moorea: Pao Pao, crête N du Mt. Fairurani. 670 m, 149°47’ W, 17°30’ S, 14 May 1987, J. Florence 8287 (holotype: P; isotypes: BISH!, PAP, US!).

Distribution. Endemic to the Society Island of Moorea at 420–800 m, where it typically occurs on high ridge slopes and crests with , , , and (Florence 1997).

40. (J. W. Moore) W. L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112718-1

Basionym: J. W. Moore, Bernice P. Bishop Mus. 16: 6. 1940. TYPE: SOCIETY ISLANDS: Tahiti: south side of Mt. Orohena, 1300 m, 14 May 1927, L. H. McDaniels 1312(holotype: BH; isotype: BISH!).

Distribution. Endemic to the Society Island of Tahiti where it is rare and localized at 900–1750 m, in cloud forest with , , and (Florence 1997).

41. W. L. Wagner & Lorence, nom. nov.

urn:lsid:ipni.org:names:77112719-1

Replaced name: Hosokawa, Trans. Nat. Hist. Soc. Taiwan 25: 22. 1935. TYPE. CAROLINE ISLANDS: Palau: Aurapushekaru I. (OropusyPageBreakakaru-to), S. of Koror I., 8 Oct 1933, T. Hosokawa 7453 (holotype: TAI; isotype: BISH!, MICH, US!, Z).

Distribution. Endemic to Palau on Babeldaob, Anguar, Ngerechong, Ulebsechel, Ulong, and the Rock Islands (Koror, Ngerukeuid, Ngeruktabel). On Babeldaob this species occurs on basaltic soils in evergreen wet forest and savannas at about 100 m elevation. On the Rock Islands it occurs on limestone substrate near sea level (2–5 m elevation) in evergreen coastal forest and cliff vegetation. This glabrous species is distinguished by its female flowers with a conical-columnar pistil 3 mm long with a cylindrical style and shortly 6–7-lobed stigma.

Etymology. We are pleased to name this species for Mr. Demei O. Otobed, president of the board of directors of the Belau National Museum, who has done so much to advance the study and conservation of Palau’s biodiversity.

Note. Some Palau collections of this species were identified as .

42. Muell. Arg, Linnaea 32 : 31. 1863.

(Müll. Arg.) Kuntze, Revis. Gen. Pl. 2: 600. 1891. TYPE. MARQUESAS ISLANDS: Nuku Hiva: D.E.S.A. Jardin 122 (lectotype: P, designated by Florence, Fl. Polynésie Française 1: 123. 1997; isolectotype: G-DC [2], P).

Müll. Arg. var. uapensis F. Br., Bernice P. Bishop Mus. Bull. 130 : 138. 1935, syn. nov. TYPE. MARQUESAS ISLANDS: Ua Pou: 9 Sep 1922, E. H. Quayle s.n. (holotype: BISH-143921! & 508277!; isotype: BISH).

Müll. Arg. var. quaylei F. Br., Bernice P. Bishop Mus. Bull. 130: 139. 1935, syn. nov. TYPE. MARQUESAS ISLANDS: Nuku Hiva: s.l., 15? Oct 1922, E. H. Quayle 1341 (holotype: BISH-508703!).

Müll. Arg. var. uahukensis F. Br., Bernice P. Bishop Mus. Bull. 130: 139. 1935, syn. nov. TYPE: MARQUESAS ISLANDS: Hiva Oa: Kopaafaa, 2770 ft, 2 Aug 1929, E.P. Mumford & A.M. Adamson 488 (lectotype: BISH-508705!; designated by St. John, Phytologia 33: 420. 1976). Additional syntypes: MARQUESAS ISLANDS: Ua Huka: s.l., 9 Nov 1922, E. H. Quayle 1781 (BISH-508704! & -143920!).

Distribution. Endemic to the Marquesas Islands (Nuku Hiva, Hiva Oa, Tahuata, Ua Pou, Ua Huka, and Fatu Hiva) where it is widespread and occurs from about 25 to 1085 m, growing in open areas or on rocky slopes and cliffs in secondary vegetation with and grasses. At higher elevations it grows among fern cover in - wet shrubland and forest (Florence 1997).

43. Hosokawa, Trans. Nat. Hist. Soc. Taiwan 25: 19. 1935. TYPE. CAROLINE ISLANDS: Palau: Babeldaob Island, near Almatin at low altitudes, 17 Sep 1933, T. Hosokawa 6921 (holotype: TAI; isotype: GH).

PageBreakDistribution. Endemic to Palau (Babeldaob, Ngemelachel, Ulong) and Rock Islands (Koror, Mecherchar, Ngerukeuid, Ngerekebesang, Ngeruktabel) where it occurs to at least 30 m elevation on volcanic soils in wet forests along streams and in savannah vegetation.

44. (J. Florence) W. L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112720-1

Basionym. J. Florence, Bull. Mus. Natl. Hist. Nat., B, Adansonia 18: 254. 1996. TYPE: SOCIETY ISLANDS: Tahiti: Papenoo, Ofetanu, 160 m, 149°26’ W, 17°38’ S, 9 Sep 1989, J. Florence 9901 (holotype: P; isotypes: BISH!, PAP).

Distribution. Endemic to the Society Island of Tahiti where it is apparently rare and known only from Papenoo Valley up to about 650 m in riparian forest with and invaded by DC. (Florence 1997).

45. Gillespie, Bernice P. Bishop Mus. Bull. 91: 18. 1932. TYPE. FIJI ISLANDS: Viti Levu: Naitasiri Province, Tamavua woods, 11 km from Suva, 150 m, 9 Aug 1927, J.W. Gillespie 2122 (holotype: BISH-508710!; isotypes: GH, UC).

Distribution. Endemic to Fiji and known only from Viti Levu at 30–1200 m (Smith 1981; Webster 1986).

46. S.L.Welsh, Flora Societensis 112. 1998.

Basionym: Baill., Adansonia 2: 239. 1862. (Baill.) Kuntze, Revis. Gen. Pl. 2: 601. 1891, non Noronha (1790). TYPE. SOC IETY ISLANDS: Tahiti: “Nouvelle-Caledonie, Port de France”, E. Vieillard 336 (holotype: P; isotype: P).

Distribution. Endemic to the Society Islands of Moorea, Raiatea, and Tahiti from 150–830 m, usually in understory of valley forest with , , and or sometimes on ridge crests. Not collected on Tahiti since the end of the 19th century but apparently still frequent on Moorea (Florence 1997).

Note. According to Florence (1997) the type of Baill. is from Tahiti, not New Caledonia. This is likely due to a labeling error.

47. (H. St. John) W. L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112721-1

Basionym. (F.Br.) H.St.John, Trans. Roy. Soc. New Zealand, Bot. 1: 187. 1962. var. pitcairnense F. Br., Bernice P. BisPageBreakhop Mus. Bull. 130: 142. 1935. TYPE: PITCAIRN ISLANDS: s.l., 1922, E. H. Quayle s.n. (holotype: BISH-508246! & -508247!).

Distribution. Endemic to the Pitcairn Islands (Henderson and Pitcairn), from about 30 to 270 m elevation. On Henderson it occurs at 30 m on eroded calcarenite in beach forest and scrub with , , and . On Pitcairn it has been collected at 270 m in secondary upland vegetation with grasses and ferns.

48. Müll. Arg., Flora 48: 388. 1865.Diasperus podocarpus (Müll. Arg.) Kuntze, Revis. Gen. Pl. 2: 600. 1891. (Müll. Arg.) C.B. Robinson, Philippine J. Sci. Bot. 6: 300. 1911. TYPE. FIJI ISLANDS: s. l., 1840, U.S. Expl. Exped. s.n. (holotype: probably G; isotype: US!).

Distribution. Endemic to Fiji and know only from the type collection.

49. (Hosokawa) W. L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112722-1

Basionym. Hosokawa, Trans. Nat. Hist. Soc. Taiwan 25: 24. 1935. TYPE: CAROLINE ISLANDS: Pohnpei: summit of Mt. Troton, 13 Aug 1933, T. Hosokawa 5770 (holotype: TAI).

Fosberg var. calvum Fosberg, Willdenowia 20: 261. 1991, syn. nov. TYPE: CAROLINE ISLANDS: Pohnpei: 1913-1914, C. L. Ledermann 13333 (holotype: B-bc100249513!).

Distribution. Endemic to Pohnpei, this species occurs from lowland wet forest up into montane cloud forest on summits from 20 to 732 m elevation.

Note. This species is characterized by its female flowers with a short, glabrous, depressed-globose ovary 0.5 mm long and glabrous columnar style 1-1.5 mm long with a 6-7-dentate stigma. Some collections of were previously identified as or .

50. W. L. Wagner & Lorence, nom. nov.

urn:lsid:ipni.org:names:77112723-1

Replaced name: P. T. Li, Acta Phytotax. Sin. 20: 117. 1982, non M. Schmid (1991). J. W. Moore, Bernice P. Bishop Mus. Bull. 226: 13. 1963, non (Baill.) Müll. Arg. (1863) nec Baill (1862). TYPE. SOCIETY ISLANDS: Raiatea: Temihani Plateau, 5 Oct 1934, H. St. John 17250 (holotype: BISH-508232!; isotype: BISH).

Note. The sheet (BISH-142814) was considered by Florence (1997) to not be part of the type because it was pubescent vs. glabrous as in the holotype. The full variation of is not well understood, but Florence accepted both specimens as this species. Without further supporting information that this really represents a mixed PageBreakcollection it seems best to accept the second sheet as an isotype. However, even if the second sheet is not accepted as an isotype, the first sheet is clearly the holotype as it was explicitly stated as such and shown in a figure in the original publication.

Distribution. Endemic to the Society Island of Raiatea where it is known from the Temehani plateau region at 435–750 m, occurring in wet forest with , , and and in open marshland with and species of Cyperaceae (Florence 1997).

51. (F. Br.) W. L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112724-1

Basionym. F. Br., Bernice P. Bishop Mus. Bull. 130: 142. 1935. TYPE. AUSTRAL ISLANDS: Raivavae: 23 Mar 1922, A. M. Stokes 43 (holotype: BISH-508248!).

Distribution. Endemic to the Austral Islands (Raivavae, Rurutu, and Tubuai). It occurs at 10–340 m in primary and secondary vegetation including riparian forest with , , , and , and on dry slopes or crests with , , , and grasses (Florence 1997).

52. (J. Florence) W. L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112725-1

Basionym. J. Florence, Bull. Mus. Natl. Hist. Nat., B, Adansonia 18: 258. 1996. TYPE. AUSTRAL ISLANDS: Rapa: flanc SE du Mt. Pukumia, 150 m, 144°19’ W, 27°36’ S, 5 Feb 1984, J. Florence 6465 (holotype: P; isotypes: BISH!, K, PAP, US!).

Distribution. Endemic to the Austral Island of Rapa, at 50–330 m in mesic forest with , , and , and sometimes on wet rocks or cliffs (Florence 1997).

53. Hosokawa, Trans. Nat. Hist. Soc. Taiwan 25: 19. 1935. TYPE. CAROLINE ISLANDS: Palau: upon a coral islet near the island of Urktable [Ngeruktabel], 15 Oct 1933, T. Hosokawa 7534 (holotype: TAI; isotype: GH, US [2]!).

Distribution. Endemic to Palau where it occurs on the Rock Islands (Ngerukeuid, Ngeruktabel, Ulong), on limestone substrate in coastal cliff vegetation near sea level to about 5 m elevation.

54. Merr., Philipp. J. Sci., C 9: 104. 1914. TYPE. MARIANA ISLANDS: Guam: hills back of Piti, 100 m, Oct 1911, R. C. McGregor 476 (lectotype: US- 01860446!, here designated).The type in PNH was destroyed during World War II.PageBreak

Distribution. Endemic to the Maraiana Islands (Guam, Alamagan, Anatahan, Pagan, Saipan, and Tinian). This species occurs in savannah vegetation.

55. W. L. Wagner & Lorence, nom. nov.

urn:lsid:ipni.org:names:77112726-1

Replaced name: J. W. Moore, Bernice P. Bishop Mus. Bull. 226: 10. 1963. TYPE. SOCIETY ISLANDS: Raiatea: S ridge of Ereeo Valley, 9 Oct 1934, H. St. John 17328 (holotype: BISH-508233!; isotype: BISH).

J.W.Moore, Bernice P. Bishop Mus. Bull. 226: 9. 1963, nom. illeg., non Yamamoto (1933). P.T.Li, Acta Phytotax. Sin. 20:117. 1982. TYPE. SOCIETY ISLANDS: Raiatea: south side of Toahiva Valley, 200 m, 7 Oct 1934, H. St. John 17305 (holotype: BISH-508155!; isotype: BISH).

Distribution. Endemic to the Society Islands (Bora Bora, Moorea, Raiatea, and Tahaa) where it occurs at 30–680 m in primary or secondary mesic or wet forest with and in valleys, or with , , and on slopes and ridges (Florence 1997).

56. (Müll. Arg.) W. L. Wagner & Lorence, comb. et stat. nov.

urn:lsid:ipni.org:names:77112727-1

Basionym: (J.R. Forst. & G. Forst.) Müll. Arg. var. samoanus Müll. Arg. in A.P.de Candolle, Prodr. 15(2): 289. 1866. J.R. Forst. & G. Forst. var. samoanum (Müll. Arg.) Pax, Bot. Jahrb. Syst. 25: 645. 1898. TYPE. SAMOAN ISLANDS: s.l., U.S. Expl. Exped. s.n. (holotype: probably G-DC).

var. samoanus Müll. Arg. in A.P.de Candolle, Prodr. 15(2):300. 1866. var. samoanum .(Müll. Arg.) Pax, Bot. Jahrb. Syst. 25:645. 1898. TYPE. SAMOAN ISLANDS: s.l., U.S. Expl. Exped. s.n. (holotype: probably G-DC).

Distribution. Endemic to the Samoan Islands (Savai`i, Upolu, Tutuila, Aunu`u, Ofu, Olosega, and Ta`u) at 60–1000 m disturbed forest, secondary forest, and pastures (Whistler 1980).

Note. Even though the varietal name was published under an illegitimate species it is legitimate under Art. 55.2 of the ICBN and is available for use at the specific level. These Samoan collections were previously referred to , butwere considered by Smith (1981) to be a separate species. He considered to be a species from New Guinea to New Hebrides [see Excluded Names].

57. (Müll. Arg.) Müll. Arg., Flora 48: 374. 1865 (as seammanianus).

PageBreakBasionym. Müll. Arg., Linnaea 32: 63. 1863 (as seemanni). (Müll. Arg.) Kuntze, Revis. Gen. Pl. 2: 600. 1891. TYPE. FIJI ISLANDS: Kadavu: s.l., 1860, B.C. Seemann 413 (holotype: probably G; isotypes: BM, K).

Müll. Arg., J., Flora 48:374. 1865. (Müll. Arg.) Kuntze, Revis. Gen. Pl. 2: 601. 1891. (Müll. Arg.) P.T.Li, Guihaia 14: 131. 1994. TYPE. FIJI ISLANDS: s.l., 1840, U.S. Expl. Exped. s.n. (Holotype: probably G; Isotypes: GH, US).

Distribution. Endemic to Fiji where it is known from Viti Levu, Ovalau, Vanua Levu, Taveuni, and Moala, but Smith (1981) thought it is most likely more widespread, at 0–1150 m, in dense dry or secondary forest or on more open hillsides.

58. (Glassman) W. L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112728-1

Basionym. Glassman, Bernice P. Bishop Mus. Bull. 209: 71. 1952. TYPE. CAROLINE ISLANDS: Pohnpei: Mt. Ninani, 731 m, 17 Aug 1949, S. Glassman 2884 (holotype: US-02158415!; isotypes: BISH, OKL).

Hosokawa, Trans. Nat. Hist. Soc. Taiwan 25:23. 1935, non Miq. ex Baill., syn. nov. (1858). TYPE. CAROLINE ISLANDS: Pohnpei: 8 Aug 1933, T. Hosokawa 5523 (holotype: TAI; isotype: US!).

Fosberg, Willdenowia 20: 260. 1991, syn. nov. TYPE. CAROLINE ISLANDS: Pohnpei: 1913-1914, C. L. Ledermann 13643x (holotype: B!).

Distribution. Caroline Islands, known from Pohnpei and Chuuk (Fano, Dublon, Nomwin, Melot Moen, Romonum, Tol, Udot, and Uman). On Pohnpei it occurs from near sea level (2 m) to 770 m in primary and secondary lowland and montane wet forest and summit cloud forest. On Moen it occurs in lowland areas among mangrove swamps near sea level and on slopes and ridges where said to be common in agroforest and secondary forest. Habitat is unknown on the other islands of Chuuk.

Note. This species is characterized by its variably pubescent stems and densely hirtellous pistil and capsules. Collections from Chuuk resemble in having a densely hirtellous ovary and style, but the pistil is comparatively shorter and only as long as the calyx lobes, and the leaves are narrowly ovate-oblong. These collections from Chuuk were previously identified as and are here tentatively included under , but may represent an undescribed species. Chuuk collections of differ in having female flowers with a glabrous pistil nearly twice as long as the calyx lobes. Some of these collections were previously identified as Certain Pohnpei collections of were previously identified as or .

59. G. L. Webster, Pacific Sci. 40: 99. 1986 (1987). TYPE. FIJI ISLANDS: Viti Levu: Rewa, woods at summit of Mt. Korombamba, 381 to 427PageBreak m, 09 Jul 1968, G.L. Webster, R. Hildreth & I. Kuruvoli 14078 (holotype: DAV; isotypes: BI, SH, GH, NY, US!).

Distribution. Endemic to Fiji on the southern part of Viti Levu at 50–430 m (Smith 1981; Webster 1986).

Note. This distinctive species was treated as sp. by Smith (1981, p.464).

60. Müll. Arg., in DC. Prodr. 15(2): 364. 1866. (Müll. Arg.) Kuntze, Revis. Gen. Pl. 2: 601. 1891. TYPE. SOCIETY ISLANDS: s. l.,1838–1842, U.S. Expl. Exped. s.n. (holotype: G-DC; isotype: US!).

Distribution. Known from the central southern Pacific region, ranging from Nauru to the Tuamotu Islands (Makatea) and Cook Islands (Aitutaki, Atiu, Mauke, and Mitiaro). Restricted to lowland calcareous substrates, usually in clearings or sunny sites in forest with , , , and (Florence 1997).

61. (Baill. ex Müll. Arg.) Müll. Arg., Flora 48: 380. 1865.

Basionym. Baill. ex Müll. Arg., Linnaea 32: 66. 1863. (Baill. ex Müll. Arg.) Kuntze, Revis. Gen. Pl. 2: 601 (1891). TYPE. SOCIETY ISLANDS: Tahiti: 1847, J. Lépine 209(holotype: G-DC; isotypes: P [3]).

(Baill. ex Müll. Arg.) Müll. Arg. var. glabrescens Müll. Arg. in A.P.de Candolle, Prodr. 15(2): 301. 1866. TYPE. SOCIETY ISLANDS: Tahiti: 1838–1842, U.S. Expl. Exped. s.n. (holotype: G-DC; isotype: US!).

J.R. Forst. & G. Forst. var. macrophyllum Müll. Arg., Linnaea 32: 63. 1863. (J.R. Forst. & G. Forst.) Müll. Arg.var. macrophyllus (Müll. Arg.) Müll. Arg., Flora 48: 374. 1865. TYPE. SOCIETY ISLANDS: Tahiti: J.A. Moerenhout s.n. (lectotype: G, designated by Florence, Fl. Polynésie Française 1: 123. 1997; isolectotype: P).

Distribution. Endemic to the Society Islands of Moorea and Tahiti where widespread and common from 50 to 1500 m, occurring from lowland wet forest with and in valleys to mid and high elevation wet forest with , , , and (Florence 1997).

62. (J. W. Moore) W. L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112729-1

Basionym. J. W. Moore, Bernice P. Bishop Mus. Bull. 226: 15. 1935. TYPE. SOCIETY ISLANDS: Raiatea: Temehani Plateau, 600 m, 5 Oct 1934, H. St. John 17279 (holotype: BISH-508231!; isotype: P).

Distribution. Endemic to the Society Islands (Huahine, Raiatea, and Tahaa) where it occurs from 0 to 600 m in lowland vegetation such as coconut plantations PageBreakand wet valleys with and to higher slopes and ridge crests with wet forest or shrubland of , , and Cyperaceae (Florence 1997).

63. (J. Florence) W. L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112730-1

Basionym. J. Florence, J.,  Fl. Polynésie Française 1: 98. 1997. TYPE. TUAMOTU ISLANDS: Niau: Maiahu, secteur oust, 146°20’ W, 16°11’ S, 2 m, 26 Mar 1990, J. Florence 10070 (Holotype: P; Isotypes: BISH!, CHR, DAV, K, L, P, PAP, PTBG!, US!).

Distribution. Endemic to the Gambier Islands (Taravai, Mangareva) and Tuamotu Islands (Niau), where it occurs from near sea level to 7–8 m on calcareous substrate. On Niau it grows in lowland forest with , , and , whereas on Taravai it was collected in secondary vegetation with and (Florence 1997).

64. G. Forst., Fl. Ins. Austral. Prodr. 65. 1786. var. virgatus (G.Forst.) Müll. Arg., Linnaea 32: 32. 1863, nom. illeg. (G.Forst.) Kuntze, Revis. Gen. Pl. 2: 597. 1891. TYPE. SOCIETY ISLANDS: Tahiti: Not designated.

Distribution. Widespread, but increasingly rare on Pacific Islands from Vanuatu, Fiji, Samoa, Tonga, Austral, Society and Cook islands (Webster 1986), and Caroline Islands (Yap) and Mariana Islands (Guam) in Micronesia, from 15 to 500 m elevation.

Note. Smith (1981) treated as native in Asia, but likely naturalized in the Pacific as did Florence (1997). Webster (1986) found a number of morphological features (smaller seeds, short fruiting pedicels, smooth to slightly roughened ovaries, and an irregularly dissected disk) that distinguish the Pacific island populations from the mainland Asian ones, and thus the Asia plants are most likely a different species, Retz. Considering these differences the Pacific island is likely a native and not found outside of Pacific islands. A complex set of considerations would be involved to make a proper lectotypification for this species. A. C. Smith (1981, p. 464) suggested that one of two collections at BM (Banks & Solander s.n.) be selected by a specialist as the lectotype. Webster (1986) incorrectly considered Smith’s comments to be a lectotypification, and Nicolson and Fosberg (2004) summarized the Cook voyage materials available, including Foster collections. They thought it inappropriate to select the Banks and Solander collection as the lectotype while also pointing out that a specialist needs to make the selection because the original material could represent a mixture of this species or Retz. or L.

65. Müll. Arg., Flora 48: 374. 1865. (Müll. Arg.) Kuntze, Revis. Gen. Pl. 2: 601. 1891. (Müll. Arg.) Gillespie,PageBreak Bernice P. Bishop Mus. Bull. 91: 17. 1932. TYPE. FIJI ISLANDS: s. l., 1840, U.S. Expl. Exped. s.n. (holotype: probably G; isotype: US!).

var. obovatum Müll. Arg., Linnaea 32: 62. 1863. var. obovatus (Müll. Arg.) Müll. Arg. in A.P.de Candolle, Prodr. 15(2): 290. 1866. TYPE. FIJI ISLANDS: Viti Levu: 1860, B. C. Seemann 412 (holotype: probably G; isotypes: BM, K).

Distribution. Endemic to Fiji and known from Viti Levu, Kadavu, Nairrai, Moala, Kanacea, and Vanua Balavu, at 0–590 m in dense dry forests, open rolling hills, and grassy slopes.

66. W.L. Wagner & Lorence, nom. nov.

urn:lsid:ipni.org:names:77112731-1

Replaced name. A.C. Sm., Fl. Vitiensis Nova 2: 486, 494. 1981, non Domin (1928). TYPE. FIJI ISLANDS: Viti Levu: Naitasiri, N portion of Rairaimatuku Plateau, between Mt. Tomanivi (Mt. Victoria) and Nasonggo, 870 to 970 m, 18 Sep 1947, A.C. Smith 6148 (holotype: BISH-142913; isotype: US!).

Distribution. Endemic to Fiji and known only from the interior of Viti Levu at 850–1150 m in dense forest (Smith 1981).

67. (Fosberg) W. L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112732-1

Basionym. Fosberg, Willdenowia 20: 262. 1991. TYPE. CAROLINE ISLANDS: Palau: 1914, C. L. Ledermann 14507 (holotype: B-bc100241068!).

Distribution. Caroline Islands, Pohnpei, known only from the type without specific locality.

Note. A glabrous species to date know only from the type collection which has only pistillate flowers. The glabrous pistil is cylindrical with a columnar style 2-2.5 mm long exserted well beyond the calyx lobes. It most closely resembles and may be conspecific with . This entity should be carefully evaluated in the context of an overall review of in Micronesia.

68. (J. Florence) W. L. Wagner & Lorence, comb. nov.

urn:lsid:ipni.org:names:77112733-1

Basionym. J. Florence, Fl. Polynésie Française 1: 99. 1997. TYPE. TUAMOTU ISLANDS: Makatea: Vaitepaua Ouest, piste de Temao, 45 m, PageBreak148°16’ W, 15°49’ S, 31 Jan 1988, J. Florence 9073 (holotype: P; isotypes: BISH!, CHR, DAV, K, P, PAP, US!).

Distribution. Endemic to the Gambier Islands (Mangareva) and Tuamotu Islands (Makatea). On Makatea it occurs from 45–75 m on calcareous substrate in primary forest with and or in degraded forest. On Mangareva it was collected in relict primary or secondary forest and cliffs up to 350 m elevation (Florence 1997).

69. Müll. Arg., in DC., Prodr. 15(2): 396. 1866. (Müll. Arg.) Kuntze, Revis. Gen. Pl. 2: 601. 1891. TYPE. FIJI ISLANDS: s. l., 610 m, 1840, U.S. Expl. Exped. s.n. (holotype: G, isotype: GH).

Distribution. Endemic to Fiji and known only from two localities: Nadarivatu, Viti Levu and Macuata Range, Vanua Levu at 100–800 m (Smith 1981).

Naturalized species

70. Schumach. & Thonn., Kongel. Danske Vidensk. Selsk. Skr., Naturvidensk. Math. Afd. 4: 195. 1829.

Distribution. Presumably native to the Neotropics, but now naturalized across tropical regions of the world; in the Pacific on Fiji, Austral,Cook, Gambier, Marquesas, Samoa, Society, Tuamotu Islands, and widespread in Micronesia (Carolines, Gilberts, Marshalls, Marianas, Nauru, and Wake) at 0–600 m elevation.

71. Klein ex Willd., Sp. Pl. 4: 582. 1805. var. debilis (Klein ex Willd.) Müll. Arg. in A.P.de Candolle, Prodr. 15(2): 407. 1866. (Klein ex Willd.) Kuntze, Revis. Gen. Pl. 2: 601. 1891.

Distribution. Native to India and Sri Lanka, but now widely naturalized; in the Pacific naturalized on Fiji, Society Islands (only Tahiti), Hawaiian Islands, and Micronesia (Caroline Islands, Mariana Islands, and Marshall Islands) at 0–450 m. Specimens from Palau referred to Nakai are .

72. Roxb., Fl. Ind., ed. 1832, 3: 668. 1832. (Roxb.) Kuntze, Revis. Gen. Pl. 2: 601. 1891.

Distribution. Origin uncertain, but now naturalized across the Indo-Pacific region and currently known from the Hawaiian Islands (Kaua`i, O`ahu, Lana`i, Maui, Hawai`i), Austral Islands (Raivavae, Rurutu, and Tubaui), Gambier (Mangareva, andPageBreak Taravai), Marquesas Islands (Nuku Hiva), Society Islands (Huahine, Moorea, Raiatea, Tahiti, and Tetiaroa), and in Micronesia the Caroline Islands (Pohnpei).

73. L., Sp. Pl.: 982. 1753. (L.) Kuntze, Revis. Gen. Pl. 2: 601. 1891.

Distribution. Native to southern Asia and now naturalized pantropically; it is naturalized across the Pacific and currently known from Fiji, Austral Islands (Rurutu), Marquesas Islands (Fatu Hiva), Society Islands (Huahine, Moorea, Raiatea, Tahaa, and Tahiti), Caroline Islands and Maraiana (Guam) Islands in Micronesia, at 0–1200 m.

Excluded names

J.R. Forst. & G. Forst., Char. Gen. Pl.: 57. 1775. Gaertn., Fruct. Sem. Pl. 2: 128. 1791, nom. illeg. (J.R. Forst. & G. Forst.) Müll. Arg., Flora 48: 374. 1865, nom. illeg., non (Aiton) Pers., Syn. Pl. 2: 591. 1807 [= (Pall.) Baill., Étude Euphorb.: 502. 1858]. (J.R.Forst. & G.Forst.) Kuntze, Revis. Gen. Pl. 2: 600. 1891. TYPE. TANNA AND AMSTERDAM ISLANDS: s. l., J.R. & G. Forster s.n. (lectotype: BM, designated by Smith, Fl. Vitiensis Nova 2: 473. 1981).

We follow Smith (1981) in considering the material previously assigned to this name from Fiji and Samoa to represent other species ( and ). We also exclude the use of the name for collections from Micronesia, and include them instead under (the majority), P. ponapense, and . There is currently no available name within for the because it would need a new name as there are two different names , both illegitimate. We provide the nomenclature for below to bring together the complex set of names involving the epithet ramiflorus. Given the uncertainty surrounding the delimitation of this species we refrain from providing a new name here.

(Pall.) Baill., Étude Euphorb. 502. 1858.

Aiton, Hort. Kew. 1: 376, nom. illeg. 1789[based on Pall.]. (Aiton) Persoon, Syn. Pl. 2: 591. 1807, nom. illeg. (Aiton) Müll. Arg. in A.P.de Candolle, Prodr. 15(2): 449. 1866, nom. illeg. (Aiton) Kuntze, Revis. Gen. Pl. 2: 592. 1891, nom. illeg.