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1 December 2014 Endemic Families of Madagascar. XIII. New, Restricted Range Species of Eremolaena Baill. and Schizolaena Thouars (Sarcolaenaceae)
Porter P. Lowry II, Louis Nusbaumer, Armand Randrianasolo, George E. Schatz, Cynthia Hong-Wa
Author Affiliations +
Abstract

Lowry II, P. P., L. Nusbaumer, A. Randrianasolo, G. E. Schatz & C. Hong-Wa (2014). Endemic Families of Madagascar. XIII. New, restricted range species of Eremolaena Baill. and Schizolaena Thouars (Sarcolaenaceae). Candollea 69: 183–193. In English, French and English abstracts.

One new species of Eremolaena Baill. and two new species of Schizolaena Thouars (belonging to the family Sarcolaenaceae) are described, illustrated and compared with the members of their respective genera they most closely resemble. Eremolaena darainensis Nusb. & Lowry is similar to Eremolaena rotundifolia (F. Gérard) Danguy but differs from it by features of the indument on the leaves and the sepals, and occurs only in the Loky-Manambato (Daraina) region of far north-eastern Madagascar, where it occurs in semi-deciduous forest on granite. Schizolaena charlotteae Lowry & G. E. Schatz resembles Schizolaena milleri Lowry & al. but is distinguished by differences in sepal indument, petal color, the number of stamens, and the length of the processes borne on the involucre in fruit. Schizolaena parvipetala Randrian. & Hong-Wa is similar to Schizolaena gereaui Lowry & al. but differs by petal size, leaf acumen length, the number of stamens, and the number of flowers per involucre. Both new species of Schizolaena Thouars are only known from lowland humid forest in far south-eastern Madagascar, in the vicinity of the city of Tolagnaro. The distribution and ecology of each species are discussed and preliminary IUCN conservation assessments are provided.

Introduction

Over the last decade and a half each of the ten genera comprising Madagascar's largest endemic family, Sarcolaenaceae, has been the subject of a synoptic revision, which collectively provide an updated taxonomic treatment of the family, including the description of 29 new species (Hong-Wa, 2009; Lowry & al., 1999, 2000, 2002; Randrianasolo & Miller, 1994, 1999; Schatz & al., 2000, 2001). Moreover, two additional species of Schizolaena Thouars have since been described (Lowry & Rabehevitra, 2006; Rabehevitra & Lowry, 2009), largely based on material collected during recent botanical inventory work, bringing the total number of recognized species from the 33 treated in the “Flore de Madagascar et des Comores” (Cavaco, 1952) to a total of 74 (Madagascar Catalogue, 2014). Further exploration, especially in areas that have previously received little or no attention, has continued to yield a wealth of new discoveries from throughout Madagascar. Here we describe three new, welldelimited species, one belonging to the genus Eremolaena Baill. occurring in semi-deciduous forests in the Loky-Manambato (Daraina) region of northeastern Madagascar, and two in Schizolaena, both of which are restricted to humid forests situated to the north of Tolagnaro in the extreme south-eastern portion of the island.

Systematics

Eremolaena darainensis Nusb. & Lowry, spec, nova (Fig. 1, 2A–D).

  • Typus: Madagascar. Prov. Antsiranana: Région SAVA, sous-préfecture de Vohemar, commune rurale de Daraina, forêt de Bekaraoka, partie N, 13°07′06″S 49°42′34″E, 420 m, 17.I.2005, fl., Nusbaumer & Ranirison LN 1420 (holo-: G [G00019278]!; iso-: K!, MO!, P [P00722548]!, TEF!).

  • Eremolaena darainensis Nusb. & Lowry differs from E. humblotiana Baill. by its smaller leaves, its flowers born singly (vs. in pairs) and its shorter sepals, and from E. rotundifolia (F. Gérard) Danguy by its stellate-lanate indument adjacent to the primary vein on the abaxial surface of the leaf (vs. absent), its smaller and less dense strigose-stellate indument on the sepals, and its presence in semi-deciduous forest on granite (vs. littoral forest on sand)

  • Small trees 8–12 m, 10–20 cm DBH, branched. Branches gray brown to reddish, glabrescent, with grayish lenticels, bark smooth; twigs of current year flattened, reddish-brown pubescent with gray to whitish stellate-strigose scattered trichomes. Leaves ovate to obovate, green, slightly discolorous, whitish on abaxial surface (brown when dry), chartaceous, 30–55 × 25–43 mm, 1-1.4(-1.7) times as long as wide, with erect white stellate indument 0.4-0.8(-1. 1) mm long on abaxial surface adjacent to the primary vein, glabrous elsewhere, base subcordate to attenuate, margin flat in dry material, irregularly and weakly undulate when fresh, apex emarginate (rarely almost round), venation brochidodromous, with (5 or) 6 to 8 pairs of alternate to subopposite secondary veins, primary and secondary veins raised below, secondary and tertiary venation dark green, brown to purplish black in dry material, with sparse stellate-strigose indument on the venation of both surfaces and along the margin; petiole 8–17 mm long, with gray to whitish stellate-strigose indument, adaxially canaliculate; stipules triangular, 1.5–3 × 1–2 mm, canaliculate, brown, with white stellate-strigose indument, caducous. Flowers solitary, erect; pedicel green, brown-blackish when dry, 4-14(-16) mm long, with sparse to dense gray to whitish stellate-strigose indument, especially toward the apex; bracts foliose, 2-4(-5) × 1-2 mm, triangular, then 1.5 × 1 mm, covered with both dense white stellate-strigose and reddish-brown indument, caducous; flower subtended by a 3-lobed collar, the lobes 1.2 × 1.5 mm, with dense whitish stellate-strigose indument, giving it a whitish cast in fresh material; sepals 5, green, blackish when dry, entire, unequal, the 2 external ones smaller, triangular to deltoid, coriaceous, 1.5–3 × 1–2 mm, green, slightly purplish when fresh, the 3 internal ones imbricate, usually clockwise but sometimes counter-clockwise, ovate, asymmetrical, 9–14 × 6– 9 mm, glabrous, coriaceous or membranaceous where overlapped by an adjacent sepal, with gray to whitish stellate-strigose indument (trichomes to 0.25–0.35 mm diam.) where overlapping an adjacent sepal, trichomes of the overlapping part less dense at anthesis on the left side than on the right side, such that the foliaceous part (blackish in dry material) is visible; petals 5, obovate, white, equal, usually overlapping counter-clockwise, sometimes clockwise, always in the opposite direction from the sepals, convoluted, sub-irregular, 19– 22 × 8–10 mm, glabrous on both surfaces, apex rounded; extrastaminal disc cupuliform, 1 mm high, with an irregular margin; stamens ca. 90 to 110, filaments slender, white, 4–8 mm long, glabrous, anthers brown, 1–2 × 1 mm, introrse, anther sacs often oblique; pollen pale yellow; ovary spherical to shortly conical, with dense, cream to yellowish stellate-strigose indument (glabrous at the apex), 3-locular; style cylindrical, erect, pale yellow, 5–6 mm long, glabrous; stigma pale yellow, 3-lobed, 2 mm long, crateriform, margin distinctly undulate. Fruit unknown.

  • Distribution and ecology. Eremolaena darainensis is restricted to the Bekaraoka and Ampondrabe forests in the Loky-Manambato (Daraina) region in north-eastern Madagascar (Fig. 3). Among the more than 54,000 individual plants documented during recent floristic inventory work and vegetation studies conducted in this area, only 39 were found of E. darainensis (Nusbaumer & al., 2011), including just two fertile trees. Eremolaena darainensis is the northernmost member of the genus, separated by nearly 250 km from the closest known locality of E. rotundifolia (F. Gérard) Danguy just north of Cap Est, and almost 350 km from the most northern population of E. humblotiana Baill. Eremolaena darainensis is only known from flowering material gathered in January and February; no fruiting collections have yet been made. It grows in semi-deciduous (transitional) forest with a dense canopy reaching to 7– 12 m and a dense under-storey of shrubs. Our new species occurs at 250–550 m elevation and is usually found on fairly steep (20-40°) slopes in fine soil on rocky outcrops. The most abundant co-occurring species include, in decreasing order, Euphorbia geroldii Rauh (Euphorbiaceae), Asteropeia amblyocarpa Tul. (Asteropeiaceae), Cleistanthus suarezensis Leandri (Phyllanthaceae), and Rinorea angustifolia (Thouars) Baill. (Violaceae).

  • Conservation status. Eremolaena darainensis is currently known form five subpopulations, all of which are encompassed within the Loky-Manambato forest, which has been accorded temporary protection by the Malagasy government as a “Station Forestière à usages Multiples” (SFUM, Multiple Use Forestry Station), which falls short of full protection, indicating that some continuing decline of the quality of the habitat can be projected. Therefore, with an Extent of Occurrence (EOO) of 81 km2, an Area of Occupancy (AOO) of 54 km2, and five locations (calculated following Callmander & al., 2007), as well as estimated number of mature individuals (based on extrapolation of the inventory data) of less than 2,500, with none of the five subpopulations estimated to contain more than 250 mature individuals, E. darainensis can be assigned a risk of extinction of “Endangered” [EN Blab(iii)+ 2ab(iii); C2a(i)] following the IUCN Red List Categories and Criteria (IUCN, 2012).

  • Notes. — Using the key to species of Eremolaena provided by Lowry & al. (2000), material of this new species would be identified as E. rotundifolia. It can, however, be distinguished from the two other members of the genus by several foliar and floral features, as well as differences in substrate preferences and geographic distribution (Fig. 3). In order to facilitate identification of material of Eremolaena, the following updated key is provided.

    Key to the species of Eremolaena Baill.

    1. Leaves subcoriaceous, largest blades at least 9 cm long, secondary and tertiary venation distinctly raised on abaxial surface; sepals 15–19 mm long at anthesis; flowers borne in pairs, subtended by 5 small, scale-like involucral lobes; humid and subhumid forest on laterite, Betampona RNI and the area E of Zahamena NP, S to near Vatomandry E. humblotiana

    1a. Leaves chartaceous, largest blade not exceeding 5(-6) cm long, secondary and tertiary venation weakly raised on abaxial surface; sepals 9–14 mm long at anthesis; flowers borne singly, subtended by a very small, 3-lobed collar 2

    2. Abaxial surface of leaves with erect stellate white trichomes 0.4-0.6(-1.1) mm long home along the midvein, apex emarginate (rarely sub-rounded), base subcordate to attenuate; sepals with stellate-strigose trichomes to 0.25–0.35 mm in diam., abaxial portion overlapped by adjacent sepal with scattered stellate-strigose trichomes revealing the foliaceous surface (blackish in dry material); semi-deciduous forest on ridge crests, granite, Loky-Manambato (Daraina) region E. darainensis

    2a. Abaxial surface of leaves without white stellate trichomes along the midvein, apex usually rounded (rarely sub-emarginate), base attenuate; sepals with stellate-strigose trichomes to 0.35–0.5 mm in diam., abaxial portion overlapped by adjacent sepal totally covered with stellate-strigose indument at anthesis, obscuring the surface; littoral forest on sand, Masoala PN to Ft. Dauphin area E rotundifolia

  • Paratypes. Madagascar. Prov. Antsiranana: Région Sava, sous-préfecture de Vohemar, commune rurale de Daraina, forêt d'Ampondrabe, 12°57′07″S 49°41′36″E, 450 m, fl., 17.II.2005, Ranirison & Nusbaumer 936 (G [G00019280]!, K!, MO!, P [P00722550]!, TEF!).

  • Fig. 1.

    Eremolaena darainensis Nusb. & Lowry. A. Branch with buds and nearly open flowers; B. Detail of adaxial surface of leaf; C. Bud with pedicel; D. Branch with buds; E. Detail of abaxial surface of leaf; F. Detail of adaxial surface of leaf.

    [A–C: Ranirison & Nusbaumer PR 936; D–F: Nusbaumer & Ranirison LN 1420] [Drawing: R. L. Andriamiarisoa]

    f01_183.jpg

    Fig. 2.

    Photographs of Eremolaena dorainensis Nusb. & Lowry (A-D) and Schizoloeno charlotteae Lowry & G. E. Schatz (E). A. Flower, from above (petals fallen); B. Detail of midvein on abaxial leaf surface showing long white stellate trichomes near the margin and small stellate-strigose indument on nerves; C. Flower, from side (2 petals remaining); D. Detail of abaxial surface of a sepal, with stellate-strigose indument on the overlapping part less dense on the left side than on the right side; E. Flower and buds with young involucres.

    [A–D: Nusbaumer & Ronirison LN 1420; E. Randriatafika & al. 653] [Photos: A–D: L. Nusbaumer; E: P. Lowry].

    f02_183.jpg

    Fig. 3.

    Geographic distribution of Eremolaena darainensis Nusb. & Lowry (stars), Schizolaena charlotteae Lowry & G. E. Schatz (circles) and Schizolaena parvipetala Randrian. & Hong-Wa (squares), mapped on the bioclimatic zones of Madagascar (after Cornet, 1974; see Schatz, 2000).

    f03_183.jpg

    Schizolaena charlotteae Lowry & G. E. Schatz, spec, nova (Fig. 2E, 4).

  • Typus: Madagascar. Prov. Toliara: Région Anosy, Bemangidy, Commune Iabokoho, Fokontany Antsotso, Ivohibe forest, 24°34′10″S 47°12′37″E, 41 m, 24.V.2006, fr., Antilahimena 4876 (holo-: MO-6564308!; iso-: G!, K!, P [P00722627]!, TAN!, WAG!).

    Schizolaena charlotteae Lowry & G. E. Schatz differs from its most similar congener, S. milleri Lowry & al., by its sparse grayish stellate indument obscuring the dark outer surface of the sepals beneath (vs. dense whitish stellate indument not obscuring the sepal surface), large petals 10– 14 mm long that are bright pinkish red grading to yellow toward the margins (vs. 7–8 mm long and white), 90 to 100 stamens (vs. ca. 265), and an involucre in fruit with processes that are 10–16 mm long and 1 mm wide below the apex (vs. 3–9 mm long and 0.2–0.5 mm wide).

  • Shrubs to trees 2–15 m tall. Twigs glabrous or sparsely hispidulose, with small, elongate lenticels. Leaves elliptic to slightly ovate or obovate, chocolate brown above (in dry material), lighter and more orangish below, subcoriaceous, (3-)4-7.5 × (1.2-) 1.5-3 cm, glabrous on both surfaces, base broadly cuneate to rounded, margin entire, minutely thickened, slightly revolute, apex acute to nearly rounded, sometimes slightly retuse, venation brochidodromous, with 6 to 9 pairs of alternate to subopposite, weakly raised secondary veins joined by rounded arches, midrib plane above, raised below; petiole 6– 9 mm long, glabrous or with scattered stellate indumentum; stipules narrowly ovate to ovate, membranous, with nearly obscure parallel venation, 10–12 × 5–7 mm, base rounded, apex acute, caducous, leaving a small scar. Inflorescence comprising 1 or 2 (rarely 3) unbranched axes, each with a pair of bracts borne near the middle and hearing 1 or 2 terminal flowers, axis ca. 10 mm in bud, expanding to 20–22 mm at anthesis, moderately to densely papillose stellate-strigose, bracts broadly elliptic to nearly circular, 4 × 3–4 mm, apex rounded, minutely stellate on abaxial surface, pubescent on adaxial surface, caducous, ultimate axes below the involucre 6–10 mm long, moderately papillose stellate, involucre in flower broadly cupuliform, with numerous cylindrical to narrowly triangular teeth, moderately to densely papillose stellate on both surfaces, containing 1 or 2 sessile flowers; sepals 3, imbricate, broadly ovate, adaxially concave, 9–10 × 6 mm at anthesis, with short stellate-papillose indumentum on the exposed part of the abaxial surface, the portion hidden by the overlapping adjacent sepal with both papillose stellate and short lanate indumentum, margins entire, the hidden portion tinged deep pinkishred, apex rounded to acute; petals 5, obovate, bright pinkish red, yellow toward the margins, slightly succulent in fresh material, chartaceous when dry, 10–14 × 6–8 mm, with dense, appressed sericeous indument in the central portion of the abaxial surface, glabrous toward the entire margins, glabrous on the adaxial surface, apex rounded to broadly acute; stamens ca. 90–100, filaments slender, ca. 4 mm long, glabrous, anthers elliptic to nearly circular, 0.8 mm long, introrse, dehiscent through longitudinal slits; ovary broadly conical, densely white woolly tomentose, 3-locular; style cylindrical, erect, ca. 9 mm long, stigma terminal, minutely 3-lobed, glabrous. Fruit subglobose, ca. 15 mm in diam., with dense stellate indumentum, most trichomes with the central branch much longer than the others, capsule dehiscent by 3 longitudinal sutures, exocarp cartilaginous, rugose, dry sepals and filaments persistent; involucre expanded, broadly cupulate, fleshy and sticky, green in nearly mature fresh material, ca. 25 × 20 mm, sparsely stellate pubescent to glabrous on both surfaces, with 5 broadly ovate, nearly equal lobes divided ca. 1/2 of the way to the base, each lobe with 7 to 10 narrowly triangular to lanceolate or cylindrical, occasionally bifid processes, each 7–16 mm long, ca. 1 mm wide just below the apex; seeds 1 per locule.

  • Distribution and ecology. Schizolaena charlotteae is known only from lowland humid forest at Bemangidy-Ivohibe, situated just a few km to the west of the village of Antsotso in the Tsitongambarika New Protected Area, which encompasses much of the Vohimena range to the north of Tolagnaro (Fig. 3).

  • Conservation status. — The sole forest (Bemangidy-Ivohibe) from which Schizolaena charlotteae is currently known has temporary protection status as part of the larger Tsitongambarika New Protected Area. However, until permanent protection has been established, the forest is still potentially subject to local disturbance and illicit exploitation, especially along its eastern edge where S. charlotteae has been collected. Therefore, with a very restricted AOO of ca. 20 km2 and only a single location, coupled with the possibility for rapid decline due to the effects of human activities if protection of the Bemangidy-Ivohibe forest is not maintained, S. charlotteae can be assigned a risk of extinction of “Vulnerable” [VU D2] following IUCN Red List Categories and Criteria (IUCN, 2012).

  • Notes. Schizolaena charlotteae is part of a morphologically coherent group of species that also includes S. laurina Baill., S. milleri Lowry & al. and S. rosea Thouars, characterized by several features including: glabrous petioles and young branches; dense, straight, appressed indumentum on the abaxial surface of the petals; ovate and usually persistent stipules and inflorescence bracts; and an involucre in fruit that is broadly to narrowly cupuliform or funnelform. Indeed, one of the collections of our new species, Service Forestier 28662, was originally assigned by Lowry & al. (1999) to S. milleri, known otherwise only from littoral forest on white sand and low elevation humid forest on latente, from near the village of Ambavala (north of Sambava) extending south to Foulpointe, fully 800 km to the north of the only known locality of S. charlotteae.

  • Using the key to species of Schizolaena provided by Lowry & al. (1999), material of this new species would be identified as S. milleri. However, it differs in several features of the flower and fruiting involucre, as indicated below in Table 1. Specimens of Service Forestier 28662 at P were originally annotated as ‘S. delphinensis’ by J.-F. Leroy, but the name was never validly published.

  • The Bemangidy-Ivohibe forest has been the focus of intensive botanical inventory conducted over the last decade by teams from the Missouri Botanical Garden and the Rio Tinto-QMM mining company in order to assess its suitability as a conservation offset site (BirdLife International, 2011; Temple & al. 2012). Dozens of new taxa have been documented from Bemangidy-Ivohibe, some of which have already been described, including new genera of Sapotaceae, Bemangidia L. Gaut. (Gautier & al., 2013) and Asteraceae, Lowryanthus Pruski (Pruski, 2014) and new species in several families such as Gnidia razakamalalana Z. S. Rogers (Thymelaeaceae; Rogers, 2006), Ivodea anosiensis Rabarim. & al. and I. macrocarpa Rabarim. & al. (Rutaceae; Rabarimanarivo & al., in press), and Micronychia bemangidiensis Randrian. & Lowry (Anacardiaceae; Randrlanasolo & Lowry, 2009).

  • Etymology. — This species is named in honor of our friend and colleague Professor Charlotte Rajeriarson, recently retired from the Université d'Antananarivo, who has played a key role in training an entire generation of Malagasy botanists, and who served as the first President of the IUCN Madagascar Plant Specialist Group, helping to ensure the successful establishment of this important national initiative.

  • Paratypes.Madagascar. Prov. Toliara: Région Anosy, Tsitongambarika, Commune Iabokoho, Fokontany Antsotso, forêt dense humide d'Ivohibe, 24°34′S 47° 11′E, 5.IV.2008, fl., Ramison & al. 581 (G, MO-6564309, P [P00722628], TEF); ibid, loc., 24°34′04″S 47°12′37″E, 90 m, 9.II.2006, fl., Randriatafika & al. 653 (MO, P [P00722633], TEF); Forêt de Bemangidy, entre les fleuves Vatomena et Manambato, au N de Ft. Dauphin, [24°34′S 47°12′E], 14.XII. 1968, fl., Service Forestier 28662 (MO-5189144, P [P00490165, P00490166]).

  • Fig. 4.

    Schizolaena charlotteae Lowry & G. E. Schatz. A. Branch with fruiting involucre; B. Flower (from above); C. Involucre surrounding mature fruit; D. Detail of leaf; [A-B, D: Antilahimena 4786; C: Randriatafika & al. 653] [Drawing: R. L. Andriamiarisoa]

    f04_183.jpg

    Table 1.

    Characters distinguishing Schizolaena charlotteae Lowry & G.E. Schatz from S. milleri Lowry & al.

    t01_183.gif

    Schizolaena parvipetala Randrian. & Hong-Wa, spec, nova (Fig. 5).

  • Typus: Madagascar. Prov. Toliara: Région Anosy, Tolagnaro, Iabokoho, Antsotso, TGK 42, forêt de Bemangidy, 24°35′17″S 47°08′42″E, 28 m, [2008], fl., Randriatafika 877 (holo-: MO-6564307!; iso-: G!, K!, MO-6406252!, P [P00722634]!, TEF!).

  • Schizolaena parvipetala Randrian. & Hong-Wa differs from its most similar congener, S. gereaui Lowry & al., by its ovate to elliptic leaves (vs. elliptic to slightly obovate) with an acumen (5-)7-14 mm long (vs. 3-6 (-12) mm), the presence of two flowers per involucre (vs. one), smaller petals measuring 4–6 × 1.8–2 mm (vs. 10–14 × 7–8 mm), 30 to 40 stamens (vs. 100 to 120) with the filaments 3–3.5 mm long (vs. ca. 1.5 mm), and styles ca. 3.5 mm long (vs. ca. 2 mm).

  • Shrubs to small trees 2–6 m tall. Twigs glabrous to sometimes sparsely pubescent, with small, roundish lenticels. Leaves ovate to elliptic, medium brown above, light brown below (in dry material), chartaceous, 2–6 × 1.2–2.4 cm, glabrous on both surfaces, base rounded to truncate, margin entire, minutely thickened, slightly revolute and undulate, apex acuminate, acumen (5-)7-14 mm long, venation brochidodromous, with 8–12 pairs of alternate to subopposite, abaxially slightly raised secondary veins joined by depressed-rounded arches, midrib slightly canaliculate above, raised below; petiole 3–5 mm long, glabrous to sparsely stellate-strigose; stipules 2, united at their base, brownish when dry, lanceolate, 2–3.5 × 1–1.5 mm, membranaceous, somewhat triplinerved, glabrous on adaxial surface, stellate on abaxial surface, base truncate, margin entire, apex acute to rounded, caducous, leaving a small scar. Inflorescences axillary, 2-4-flowered, with 1 or 2 unbranched axes, each with a pair of basally connate bracts borne in the middle and bearing 2 terminal flowers, axes 2–3 mm long in bud, reaching 8 mm long at anthesis, densely short stellate, bracts brownish, widely ovate, 1 × 1.2 mm, base truncate, glabrous on adaxial surface, densely stellate on abaxial surface, membranaceous, caducous, leaving a rimmed scar, margin entire, apex rounded, ultimate axes below the involucre 1.5–4.5 mm long, densely stellate, involucre in flower a shallowly 5-lobed rim, densely papillose stellate on both surfaces, subtending 2 sessile flowers, lobes minutely crenate; sepals 3, imbricate, broadly ovate, adaxially concave, 3–4 × 2.5–2.8 mm at anthesis, glabrous on adaxial surface, densely stellate on the exposed part of the abaxial surface, the portion hidden by the overlapping adjacent sepal glabrous and darker-colored, base truncate, margin entire, apex acute to rounded, occasionally shallowly bifid; petals 5, white, oblong, chartaceous (in dry material), 4–6 × 1.8–2 mm, glabrous on both surfaces, base truncate, margin entire, apex rounded, caducous; disc cupuliform, denticulate, 0.8-1 mm long; stamens 30 to 40, filaments slender, often contorted in dry material, 3–3.5 mm long, glabrous, anthers ovoid to subglobose, 0.3–0.4 mm long, introrse, dehiscent through longitudinal slits; ovary ovoid to subglobose, 1.5–2.5 × 2 mm, densely white tomentose, 3-locular, style cylindrical, contorted in dry material, ca. 3.5 mm long, stigma terminal, truncate to slightly 3-lobed, glabrous. Fruit unknown.

  • Distribution and Ecology.Schizolaena parvipetala, like S. charlotteae described above, appears to be restricted to lowland humid forest of southeastern Madagascar, where it has been recorded to the W of Mahatalaky and at Bemangidy-Ivohibe in the Tsitongambarika New Protected Area, respectively ca. 20 and 55 km N of Tolagnaro (Fig. 3).

  • Conservation status. Schizolaena parvipetala is known from only two localities, one of which (Bemangidy-Ivohibe) currently has temporary protection (but see the assessment of Schizolaena charlotteae above) while the other (W of Mahatalaky) lacks any protection. Therefore, with an AOO of ca. 20 km2 and projected continuing decline as a result of forest conversion and degradation at the second location, S. parvipetala can be assigned a risk of extinction of “Endangered” [EN B2ab(ii,iii,iv,v)] following IUCN Red List Categories and Criteria (IUCN, 2012).

  • Notes. As its name suggests, Schizolaena parvipetala stands out by having the smallest flowers of any member of the genus. It closely resembles S. gereaui, which also occurs in south-eastern Madagascar, and specimens would be identified as that species using the key provided by Lowry & al. (1999). However, S. parvipetala differs by several foliar and floral characters, as summarized in Table 2.

  • Paratypes. Madagascar. Prov. Toliara: Région Anosy, Tolagnaro, Iabokoho, Antsotso, TGK 42, forêt de Bemangidy, 24°35′17″S 47°08′42″E, 28 m, s.d., fl., Randriatafika 876 (MO-6407630, P [P00722635], TAN); Mahatalaky, Farafara Vatambe, forêt humide de basse altitude de Farafara Andohavolo située au S du village de Farafara, 24°51′05″S47°00′07″E, 179 m, 19.II.2009, fr., Rakotovao 4343 (G!, K!, MO-6404251, P [P00722636], TAN. WAG!).

  • Fig. 5.

    Schizolaena parvipetala Randrian. & Hong-Wa A. Branch with flowers; B. Detail of leaf; C. Peduncle with 2 flowers subtended by undeveloped involucre. [Randriatafika 877] [Drawing: R. L. Andriamiarisoa]

    f05_183.jpg

    Table 2.

    Characters distinguishing Schizolaena parvipetala Randrian. & Hong-Wa from S. gereaui Lowry & al.

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    Acknowledgements

    We wish to thank Roger Lala Andriamiarisoa for the fine illustrations, and the flora team of Rio Tinto-QMM (Johny Rabenantoandro, Faly Randriatafika, David Rabehevitra and Roger Ramison) for providing excellent collections and assistance in the field in SE Madagascar. We are also very grateful for the valuable comments on the manuscript provided by Sven Buerki, Martin Callmander and an anonymous reviewer. LN is grateful to Laurent Gautier, Rodolphe Spichiger and Pierre-André Loizeau for support, Patrick Ranirison for providing herbarium specimens, and Felipe Castaño for assistance with the preparation of material for microscopic observation. Fieldwork by MBG botanists was conducted under collaborative agreements between the Missouri Botanical Garden and the Parc Botanique et Zoologique de Tsimbazaza and the Direction de la Recherche Forestière et Piscicole, FOFIFA, Antananarivo, Madagascar. Research conducted by MBG staff was supported by the U.S. National Science Foundation (grant no. 0743355 to GES and PPL), the Andrew W. Mellon Foundation, and Rio Tinto-QMM. Research carried out by LN in Daraina was funded in part by the Conservatoire et Jardin botaniques de la Ville de Genève, the University of Geneva, Conservation International (CBC fund), the Malagasy NGO Fanamby, the Fondation Jean-Marcel Aubert, and the Vontobel Stiftung. We gratefully acknowledge courtesies extended by the Government of Madagascar (Direction Générale de la Gestion des Ressources Forestières) and the Département de Biologie et Ecologie Végétale de l'Université d'Antananarivo.

    References

    1.

    BirdLife International (2011). Tsitongambarika Forest, Madagascar. Biological and socio-economic surveys, with conservation recommendations. BirdLife International, Cambridge. Google Scholar

    2.

    M. W. Callmander , G. E. Schatz , P. P. Lowry II, M. O. Laivao , J. Raharimampionona , S. Andriambololonera , T. Raminosoa & T. K. Consiglio (2007). Identification of priority areas for plant conservation in Madagascar using IUCN Red List criteria: rare and threatened Pandanaceae indicate sites in need of protection. Oryx 41: 168–176. Google Scholar

    3.

    A. Cavaco ( 1952). Chlaenaceae. In : H. Humbert (ed.), Fl. Madagascar Comores 126: 1–37. Google Scholar

    4.

    A. Cornet (1974). Essai de cartographie bioclimatique à Madagascar. Notice Explicative No. 55. ORSTOM, Paris. Google Scholar

    5.

    L. Gautier , Y. Naciri , A. A. Anderberg , J. E. E. Smedmark , R. Randrianaivo & U. Swenson (2013). A new species, genus and tribe of Sapotaceae, endemic to Madagascar. Taxon 62: 972– 983. Google Scholar

    6.

    C. Hong-Wa ( 2009). Endemic families of Madagascar. XII. Resurrection and taxonomic revision of the genera Mediusella (Cavaco) Hutchinson and Xerochlamys Baker (Sarcolaenaceae). Adansonia ser. 3, 31: 311–339. Google Scholar

    7.

    IUCN (2012). IUCN Red List Categories and Criteria: Version 3.1. 2nd Edition. IUCN Species Survival Commission, Gland & Cambridge. Google Scholar

    8.

    P. P. Lowry II , T. Haevermans , J.-N. Labat , G. E. Schatz , J.-F. Leroy & A.-E. Wolf (2000). Endemic families of Madagascar. V. A synoptic revision of Eremolaena, Pentachlaena and Perrierodendron (Sarcolaenaceae). Adansonia ser. 3, 22: 11–31. Google Scholar

    9.

    P. P. Lowry II & D. Rabehevitra ( 2006). Endemic families of Madagascar. IX. A new littoral forest species of Schizolaena (Sarcolaenaceae). Adansonia ser. 3, 28: 149–153. Google Scholar

    10.

    P. P. Lowry II , G. E. Schatz , J.-F. Leroy & A.-E. Wolf ( 1999). Endemic families of Madagascar. III. A synoptic revision of Schizolaena (Sarcolaenaceae). Adansonia ser. 3, 21: 183–212. Google Scholar

    11.

    P. P. Lowry II , G. E. Schatz & A.-E. Wolf ( 2002). Endemic families of Madagascar. VIII. A synoptic revision of Xyloolaena Baill. (Sarcolaenaceae). Adansonia ser. 3, 24: 7–19. Google Scholar

    12.

    Madagascar Catalogue (2014). Catalogue of the Vascular Plants of Madagascar. Missouri Botanical Garden, St. Louis & Antananarivo [  www.tropicos.org/project/mada ]. Google Scholar

    13.

    L. Nusbaumer ( 2011). Species distribution patterns in steep environmental gradients: downscaling of a biogeographical framework (Loky-Manambato Region, NE Madagascar). Ph. D. thesis, University of Geneva. Google Scholar

    14.

    J. Pruski ( 2014). Lowryanthus rubens (Compositae: Athroismeae), a new genus and species from southeastern Madagascar. Phytoneuron 51: 1–11. Google Scholar

    15.

    M. N. Rabarimanarivo , N. H. Rakotonirina , P. B. Phillipson , P. P. Lowry II, J.-N. Labat & M. Pignal (in press). Révision du genre Ivodea Capuron (Rutaceae), endémique de Madagascar et des Îles Comores. Adansonia ser. 3. Google Scholar

    16.

    D. Rabehevitra & P. P. Lowry II ( 2009). Endemic families of Madagascar. XI. A new critically endangered species of Schizolaena (Sarcolaenaceae) from tapia woodland in South-Central Madagascar. Adansonia ser. 3, 31: 149–155. Google Scholar

    17.

    A. Randrianasolo & P. P. Lowry II ( 2009). Four new species and one new combination in the Malagasy endemic genus of Micronychia Oliv. (Anacardiaceae). Adansonia ser. 3, 31: 157–168 Google Scholar

    18.

    A. Randrianasolo & J. S. Miller ( 1994). Sarcolaena isaloensis, a new species of Sarcolaenaceae from Isalo, south-central Madagascar. Novon 4: 290–292. Google Scholar

    19.

    A. Randrianasolo & J. S. Miller ( 1999). Taxonomic revision of the genus Sarcolaena (Sarcolaenaceae). Ann. Missouri Bot. Gard. 86: 702–722. Google Scholar

    20.

    Z. A. Rogers ( 2006). A new species of Malagasy Gnidia and the lectotypification of Octolepis decalepis (Thymelaeaceae). Adansonia ser. 3, 28: 155–160. Google Scholar

    21.

    G. E. Schatz 2000. Endemism in the Malagasy tree flora. In : W. R. & S. Lourenço S. M. Goodman (ed.), Diversity and endemism in Madagascar : 1–9. Mémoires de la Société de Biogéographie, Paris. Google Scholar

    22.

    G. E. Schatz , P. P. Lowry II & A.-E. Wolf ( 2000). Endemic families of Madagascar. VI. A synoptic revision of Rhodolaena (Sarcolaenaceae). Adansonia ser. 3, 22: 239–252. Google Scholar

    23.

    G. E. Schatz , P. P. Lowry II & A.-E. Wolf ( 2001). Endemic families of Madagascar. VII A synoptic revision of Leptolaena Thouars sensu stricto (Sarcolaenaceae). Adansonia ser. 3, 23: 171–189. Google Scholar

    24.

    H. J. Temple , S. Anstee , J. Ekstrom , J. D. Pilgrim , J. Rabenantoandro , J.-B. Ramanamanjato , F. Randriatafika & M. Vincelette (2012). Forecasting the path towards a Net Positive Impact on biodiversity for Rio Tinto QMM. IUCN, Gland. Google Scholar
    © CONSERVATOIRE ET JARDIN BOTANIQUES DE GENEVE 2014
    Porter P. Lowry II, Louis Nusbaumer, Armand Randrianasolo, George E. Schatz, and Cynthia Hong-Wa "Endemic Families of Madagascar. XIII. New, Restricted Range Species of Eremolaena Baill. and Schizolaena Thouars (Sarcolaenaceae)," Candollea 69(2), 183-193, (1 December 2014). https://doi.org/10.15553/c2014v692a11
    Received: 15 September 2014; Accepted: 6 October 2014; Published: 1 December 2014
    KEYWORDS
    conservation
    Eremolaena
    Madagascar
    new species
    SARCOLAENACEAE
    Schizolaena
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